Sample records for albite

  1. In situ viscosity measurements of albite melt under high pressure

    CERN Document Server

    Funakoshi, K I; Terasaki, H


    The viscosities of albite (NaAlSi sub 3 O sub 8) melt under high pressures have been measured using an x-ray radiography falling sphere method with synchrotron radiation. This method has enabled us to determine the precise sinking velocity directly. Recent experiments of albite melt showed the presence of a viscosity minimum around 5 GPa (Poe et al 1997 Science 276 1245, Mori et al 2000 Earth Planet. Sci. Lett. 175 87). We present the results for albite melt up to 5.2 GPa at 1600 and 1700 deg. C. The viscosity minimum is clearly observed to be around 4.5 GPa, and it might be explained not by the change of the compression mechanism in albite melt but by change of the phase itself.

  2. Experimental studies of interaction between water and albite melts

    Institute of Scientific and Technical Information of China (English)

    SUN; Qiang; (孙樯); XIE; Hongsen; (谢鸿森); ZHENG; Haifei; (郑海飞); GUO; Jie; (郭捷); DING; Dongye,(丁东业)


    On the basis of FTIR and Raman spectra studies on hydrous albite glasses, it is found that there exist two water solubility mechanisms in albite melts simultaneously. On the one hand, water interacts with Al -O°-Al to produce the Q3 Al-OH, leading to depolymerization, and this results in the appearance of 4500 cm(1 in FTIR spectra and 900 cm(1 in Raman spectra. On the other hand, the exchange of H+ in water with Na+ in albite melt as charge-balancing cation occurs at the same time. In the initial stage, the production of Al -OH is the dominant solubility mechanism, at the stage of higher water contents, the exchange of H+ with Na+ becomes the important dissolution mechanism. The dissolution of water into albite melt can be expressed as H2O+ 3NaAlSi3O8 = 2NaAl(OH)Si3O7.5 +HAlSi3O8 +NaOH.

  3. Radioluminescence and thermoluminescence of albite at low temperature

    Energy Technology Data Exchange (ETDEWEB)

    Can, N., E-mail: [Physics Department, Faculty of Arts and Sciences, Celal Bayar University, 45140 Muradiye-Manisa (Turkey); Garcia-Guinea, J. [Museo Nacional Ciencias Naturales, Jose Gutierrez Abascal 2, Madrid 28006 (Spain); Kibar, R.; Cetin, A.; Ayvacikli, M. [Physics Department, Faculty of Arts and Sciences, Celal Bayar University, 45140 Muradiye-Manisa (Turkey); Townsend, P.D. [Science and Technology, University of Sussex, Brighton BN1 9QH, England (United Kingdom)


    Feldspar as an archaeological and geological natural material for dating and retrospective dosimetry is receiving more and more attention because of its useful luminescence properties. In this study, the 25-280 K thermoluminescence (TL) and radioluminescence (RL) spectra in albite, which is a component of the two main feldspar series, the alkali feldspar (Na, K)AlSi{sub 3}O{sub 8} and the plagioclases (NaAlSi{sub 3}O{sub 8}-CaAl{sub 2}Si{sub 2}O{sub 8}) have been presented for aliquots along (001) and (010) crystallographic orientations. There are four main emission bands that are considered to arise from complexes of intrinsic defects linked in larger complexes with impurities such as Na{sup +}, Mn{sup 2+} or Fe{sup 3+} ions. The consequence of their association is to produce different luminescence efficiencies that produce wavelength sensitive TL curves. Radioluminescence data at low temperature for albites is distorted by contributions from the TL sites, even when the RL is run in a cooling cycle. This indicates the potential for a far more general problem for analysis of low temperature RL in insulating materials. - Highlights: > TL and RL spectra in albite were presented for different orientations. > There are 4 emission bands that are considered to arise from complexes of intrinsic. > RL data at low temperature for albite is distorted by contributions from TL sites. > This indicates the potential problem for analysis of low temperature RL.

  4. Adsorption of N-tallow 1,3-propanediamine-dioleate collector on albite and quartz minerals, and selective flotation of albite from greek stefania feldspar ore. (United States)

    Vidyadhar, A; Hanumantha Rao, K; Forssberg, K S E


    The adsorption behavior of tallow 1,3-propanediamine-dioleate (Duomeen TDO) collector on albite and quartz minerals is assessed through Hallimond flotation, zeta potential, and diffuse reflectance FTIR investigations, together with the species distribution of the collector. The collector performance on albite separation from a natural feldspar material is evaluated in bench scale flotation tests. The Hallimond flotation responses of the minerals as a function of pH and collector concentration indicate that albite can be selectively floated from quartz at pH 2 where the doubly positively charged collector species adsorb on albite but not on quartz. However, the zeta potential and infrared spectra reveal that the adsorption behavior of the collector is similar on both minerals. The discrepancy in the flotation and adsorption results is attributed to the coarse and fine particle size fractions, and the shorter and longer equilibration periods employed in these studies respectively. The comparable adsorption on fine particles of albite and quartz at pH 2 is explained by the interaction of ammonium ions on silanol groups by hydrogen bonding as well as electrostatic interactions. The changes in zeta potentials are in good agreement with the formation of ionic species and free molecular forms of the collector. The IR spectra show the coexistence of neutral oleic acid together with charged amine species at low pH values in accordance with the species distribution diagram. Selective flotation of albite is accomplished from a natural feldspar material with tallow diamine-dioleate collector at pH 2 using sulfuric acid, only when the feed is deslimed prior to the bench scale flotation tests. An albite recovery exceeding 85% is achieved from a feed material containing about 50% albite.

  5. Mineralogy and petrograghy of some tin, lithium and beryllium bearing albite-pegmatites near Doade, Galicia, Spain

    NARCIS (Netherlands)

    Hensen, B.J.


    The petrography and mineralogy of some Hercynian albite-pegmatites near Doade, Galicia, Spain is described. The mineral assemblage consists of albite, K-feldspar, quartz, muscovite, spodumene, petalite, cassiterite, beryl, columbitetantalite, montebrasite, apatite, eosphorite-childrenite, zircon, to

  6. Authigenic albite formation due to water-rock interactions - Case study: Magnus oilfield (UK, Northern North Sea) (United States)

    Mu, Nana; Fu, Yunjiao; Schulz, Hans-Martin; van Berk, Wolfgang


    It is the aim of this contribution to test whether organic-inorganic interactions could induce the formation of authigenic albite. This concept and related results are being compared with modelling scenarios which are purely based on inorganic geochemical reactions. In order to unravel the pathway of authigenic albite formation, this paper presents results of a multidisciplinary study from imaging, geochemistry, mineralogy, and hydrogeochemical modelling. The Jurassic reservoir sandstones of the Magnus oilfield (UK, North Sea) were chosen as a test site. Albite occurs with 4-18 wt.% in the Magnus sandstones and its contents vary with depth. However, albite contents increase with increasing K-feldspar contents and decreasing grain size. It occurs in three forms: (1) as lamellae in perthite, (2) as overgrowth on/in corroded feldspar, and, (3) as cloudy replacing albite patches in K-feldspar. The albite overgrowth has the highest chemical purity (100% albite) whilst albite lamellae and replacing albite patches are slightly less pure (containing 1-4% anorthite). Albite appears non-altered, and has a euhedral morphology and dull cathodoluminescence. It commonly co-occurs with corroded K-feldspar grains. The precipitation of diagenetic albite in the Magnus sandstones is attributed to deep burial 80 Ma ago and may have continued until today at temperatures between 90-120 °C. The results of hydrogeochemical modelling offer two possible pathways for the authigenic albite formation: (1) Dissolution of unstable minerals (such as kaolinite and chalcedony) coupled to reduction of ferric iron minerals by products generated during oil generation, migration and degradation; (2) Dissolution of non-end member feldspar, such as K-feldspar with 10% albite, coupled to illite formation can account for trace amounts of albite due to an elevated Na+/K+ activity ratio in the pore water.

  7. Albitization and redistribution of REE and Y in IOCG systems: Insights from Moonta-Wallaroo, Yorke Peninsula, South Australia (United States)

    Kontonikas-Charos, Alkis; Ciobanu, Cristiana L.; Cook, Nigel J.


    Trace element concentrations, particularly rare earth elements and yttrium (REY) in feldspars and accessory minerals, have been determined in a suite of albitized igneous, metasedimentary and metasomatite rocks from the Moonta-Wallaroo district, Olympic Cu-Au Province, South Australia. Results show that changes in REY-fractionation trends and concentrations in feldspars and common accessories are associated with key textures in albite-bearing associations from different lithologies. In granitic rocks, pseudomorphic replacement of pre-existing feldspars is typified by porous albite with cleavage-oriented intergrowths of sericite and pore-attached hematite. These observations are comparable with albitization features of granitic terranes elsewhere. A mineral association (albite-sericite ± chlorite), similar to that from granitoids, is observed as pervasive spots in limestone, inferring prograde skarnoid reactions at low fluid/rock ratio in an impure carbonate. In metasedimentary and metasomatite rocks with comparable Na2O content (~ 5-6 wt.%), fine-grained granoblastic albite suggests growth under high fluid/rock ratios irrespective of lithology. In such cases, albite with the highest REY content (ΣREY ~ 200 ppm) accounts for the entire REY budget, e.g., in albite-biotite-schist with the lowest abundance of accessory minerals. Nanoscale investigation confirms this albite to be a REY carrier (elements incorporated within the crystal lattice); no pore-attached inclusions are observed. In contrast, albite with the lowest REY-concentration (~ 14 ppm) is encountered in the metasomatite. In such rocks, recording the highest ΣREY (~ 1000 ppm) in whole-rock, partitioning of REY is favoured among the abundant accessories (titanite, apatite) and calc-silicates (actinolite, clinozoisite) rather than albite. Comparable low-REY albite is also found in granitoid-derived albitite (Na2O ~ 5 wt.%), in which abundant accessories and discrete REY-minerals formed during albitization

  8. Ferropseudobrookite-silica mineral-albite-chondrule in the ALH-77015 chondrite (L3)




    Ferropseudobrookite-silica mineral-albite-chondrule was found in an unequilibraed (L3) chondrite (ALH-77015). This is the first finding of ferropseudobrookite in chondrite. The ferropseudobrookite exhibits a weakly zonal structure. The stability field of ferropseudobrookite suggests that the chondrule should have been quenched at a temperature near 1140±10℃.

  9. Evidence for a new type of regenerated thermoluminescence in an albite

    Energy Technology Data Exchange (ETDEWEB)

    Gartia, R.K. (Manipur Univ., Imphal (India). Dept. of Physics); Robertson, G.B. (Adelaide Univ. (Australia))


    While recording the natural thermoluminescence (TL) of a feldspar (Amelia albite) it has been found that if the heating is not sufficient to clean out the high-temperature peak which occurs around 550-575{sup 0}C, a new peak at about 300{sup 0}C occurs on the next heating. This new observation of regeneration of TL is different from the regenerated TL reported in the literature, and seems to be due to a localized, thermally assisted mechanism. (author).

  10. Geomorphological stability of Permo-Triassic albitized profiles - case study of the Montseny-Guilleries High (NE Iberia) (United States)

    Parcerisa, D.; Casas, L.; Franke, C.; Gomez-Gras, D.; Lacasa, G.; Nunez, J. A.; Thiry, M.


    Massif paleoalteration profiles (≥ 200 m) occur in the upper parts of the Montseny-Guilleries High (NE Catalan Coastal Ranges). The profiles consist of hard albitized-chloritized-hematized facies in the lower part and softer kaolinized-hematized facies in the upper part of the section. Preliminary paleomagnetic data show Triassic ages for both, the albitized and the kaolinized parts, and point to a surficial formation altered under oxidising conditions. Similar paleoalteration profiles have already been described and dated to Triassic ages elsewhere in Europe [Schmitt, 1992; Ricordel et al., 2007; Parcerisa et al., 2009]. These Permian-Triassic alterations are following a succession of different mineral transformations from the top to the base of the profile: 1) Red facies are defined by an increase in the amount and size of haematite crystals leading to the red colour of the rocks. The increase on haematite content is pervasively affecting the whole rock and is accompanied by the kaolinitization of the feldspars. 2) Pink facies: here, the granite shows an uniform pink colouration, which is mainly due to the albitization of the primary Ca-bearing plagioclases, accompanied by a precipitation of minute haematite, sericite, and calcite crystals inside the albite. Additionally primary biotite is fully chloritized. The pink granites are much more resistant to the present-day weathering than the "unaltered" facies at the base of the profile. 3) Spotted facies is characterized by a partial alteration of the rock, which caused a pink-screened aspect to the rock. The alteration developed along the fractures and is less well developed or absent in the non-fractured zones. In the pink-screened facies, the plagioclases are partially albitized and contain numerous hematite inclusions. Biotites are usually almost entirely chloritized. 4) Unaltered facies: These granites are coloured white to greyish, containing plagioclase and K-feldspar that do not show any trace of

  11. A thermochemical calculation of the pyroxene saturation surface in the system diopside-albite-anorthite (United States)

    Hon, R.; Henry, D. J.; Navrotsky, A.; Weill, D. F.


    The pyroxene saturation surface in the system diopside-albite-anorthite may be calculated to + or - 10 C from thermochemical data over most of its composition range. The thermochemical data used are the experimentally determined enthalpies of mixing of the ternary liquids and the enthalpy of fusion of diopside. These are combined with a mixing model for the configurational entropy in the melt and the activity of CaMgSi2O6 in the clinopyroxene, which is less than unity due to departures from CaMgSi2O6 stoichiometry. The two-lattice melt model appears to work satisfactorily throughout the pyroxene primary phase field but probably needs modification at more anorthite-rich compositions.

  12. The combined effect of temperature and pH on albite dissolution rate under far-from-equilibrium conditions (United States)

    Gruber, Chen; Kutuzov, Ilya; Ganor, Jiwchar


    Two of the most studied aspects of albite dissolution kinetics are the effects of temperature and pH. Previous studies quantified the effect of pH on albite dissolution rate under constant temperature. These studies suggested that the effect of pH on dissolution rate can be attributed to three independent dissolution mechanisms that are dominant in different pH region: acidic - proton-promoted, neutral - water-promoted and alkaline - hydroxide-promoted. Based on experimental results, those studies developed a rate law to predict albite dissolution rate as a function of pH, assuming that the effect of pH is temperature independent. The effect of temperature was attributed either to the temperature dependency of the rate under constant pH or that of the rate law coefficients. Nevertheless no unified rate law that combines both effects was suggested. When applying the effects of temperature and pH assuming they are independent of each other in order to predict the dissolution rate at pH of about 5 and various temperatures, the predicted rate overestimate the rate by 0.5-1 order of magnitude. The current study develops and suggests the use of new rate law that is based on two fast adsorption reactions of protons and hydroxides on two different surface sites. The new rate law considers the effect of surface coverage of protons and hydroxides that is temperature dependent. The new rate law successfully describes the variation of albite dissolution rate (about 8 orders of magnitude) under wide temperature (3.6-300 °C) and pH (1.20-12.40) ranges. Under slightly acidic conditions (pH 5-7) the new rate law predicts a minimum rate zone that was not observed before. In order to confirm whether this minimum rate zone does exist, three SPBE (single-point-batch-experiment) of albite dissolution were conducted at pH 5 and temperatures of 3.6, 25 and 50 °C. The SPBE experiments confirm the existence of minimum rate zone predicted by the independent new rate law. The new rate law

  13. Correlation of the Na/K ratio in geothermal well waters with the thermodynamic properties of low albite and potash feldspar

    Energy Technology Data Exchange (ETDEWEB)

    Apps, J.A.; Chang, G.M.


    The Na/K ratio in geothermal well waters provides a better estimate of the relative stability of low albite and potash feldspar than do predictions from calorimetry and high temperature phase equilibria. The calculated saturation indices from field data for low albite, potash feldspar suggest that [Delta]G[sub f,298][sup o] for the latter should be revised to [minus]3748.6[plus minus]3.7 kJ.mol[sup [minus]1].

  14. Correlation of the Na/K ratio in geothermal well waters with the thermodynamic properties of low albite and potash feldspar

    Energy Technology Data Exchange (ETDEWEB)

    Apps, J.A.; Chang, G.M.


    The Na/K ratio in geothermal well waters provides a better estimate of the relative stability of low albite and potash feldspar than do predictions from calorimetry and high temperature phase equilibria. The calculated saturation indices from field data for low albite, potash feldspar suggest that {Delta}G{sub f,298}{sup o} for the latter should be revised to {minus}3748.6{plus_minus}3.7 kJ.mol{sup {minus}1}.

  15. Albite feldspar dissolution kinetics as a function of the Gibbs free energy at high pCO_2

    CERN Document Server

    Hellmann, Roland; Tisserand, Delphine; Renard, François


    We are currently measuring the dissolution kinetics of albite feldspar at 100 deg C in the presence of high levels of dissolved CO_2 (pCO_2 = 9 MPa) as a function of the saturation state of the feldspar (Gibbs free energy of reaction, \\Delta G). The experiments are conducted using a flow through reactor, thereby allowing the dissolution reactions to occur at a fixed pH and at constant, but variable saturation states. Preliminary results indicate that at far-from-equilibrium conditions, the dissolution kinetics of albite are defined by a rate plateau, with R \\approx 5.0 x 10^{-10} mol m^{-2} s^{-1} at -70 -40 kJ mol^{-1}, the rates decrease sharply, revealing a strong inverse relation between the dissolution rate and free energy. Based on the experiments carried out to date, the dissolution rate-free energy data correspond to a highly non-linear and sigmoidal relation, in accord with recent studies.

  16. Radiation damage-controlled localization of alteration haloes in albite: implications for alteration types and patterns vis-à-vis mineralization and element mobilization (United States)

    Pal, D. C.; Chaudhuri, T.


    Uraninite, besides occurring in other modes, occurs as inclusions in albite in feldspathic schist in the Bagjata uranium deposits, Singhbhum shear zone, India. The feldspathic schist, considered the product of Na-metasomatism, witnessed multiple hydrothermal events, the signatures of which are preserved in the alteration halo in albite surrounding uraninite. Here we report radiation damage-controlled localization of alteration halo in albite and its various geological implications. Microscopic observation and SRIM/TRIM simulations reveal that the dimension of the alteration halo is dependent collectively on the zone of maximum cumulative α dose that albite was subjected to and by the extent of dissolution of uraninite during alteration. In well-preserved alteration haloes, from uraninite to the unaltered part of albite, the alteration minerals are systematically distributed in different zones; zone-1: K-feldspar; zone-2: chlorite; zone-3: LREE-phase/pyrite/U-Y-silicate. Based on textures of alteration minerals in the alteration microdomain, we propose a generalized Na+➔K+➔H+ alteration sequence, which is in agreement with the regional-scale alteration pattern. Integrating distribution of ore and alteration minerals in the alteration zone and their geochemistry, we further propose multiple events of U, REE, and sulfide mineralization/mobilization in the Bagjata deposit. The alteration process also involved interaction of the hydrothermal fluid with uraninite inclusions resulting in resorption of uraninite, redistribution of elements, including U and Pb, and resetting of isotopic clock. Thus, our study demonstrates that alteration halo is a miniature scale-model of the regional hydrothermal alteration types and patterns vis-à-vis mineralization/mobilization. This study further demonstrates that albite is vulnerable to radiation damage and damage-controlled fluid-assisted alteration, which may redistribute metals, including actinides, from radioactive minerals

  17. Albitization and quartz dissolution in Paleoproterozoic metagranite, central Sweden — Implications for the disposal of spent nuclear fuel in a deep geological repository (United States)

    Petersson, Jesper; Stephens, Michael B.; Mattsson, Håkan; Möller, Charlotte


    Hydrothermal alteration resulting in albitization and quartz dissolution has been identified in Paleoproterozoic metagranites down to - 1000 m elevation at Forsmark, Sweden. The alteration features were discovered during investigations to locate a site for the disposal of spent nuclear fuel in a deep geological repository. In general, albitization occurs extensively, but it is also observed locally adjacent to minor intrusive bodies of amphibolite. The altered rocks show a marked decrease in K-feldspar and an increase in quartz relative to the unaltered equivalents, resulting in an epitonalitic composition. Plagioclase is metamorphic in character and generally richer in albite than in the unaltered rocks. It is inferred that albitization was triggered by the input of basic or intermediate melts into the crust during igneous activity close to the peak of regional metamorphism at 1.87-1.86 Ga. The mineralogy of the epitonalites gives rise to an increased thermal conductivity and, thereby, a positive influence for the design and safety of a deep geological repository for spent nuclear fuel. However, the increased frequency of low conductive amphibolite in the albitized volumes, consistent with the proposed mechanism for alteration, gives a negative influence. In sharp contrast to the albitization, a majority of the occurrences of quartz dissolution, which resulted in the formation of episyenite, are located along fracture zones. Quartz dissolution took place between or after 1.8-1.7 Ga, when the bedrock was able to respond to deformation in a brittle manner. Most of the vugs left after the removal of quartz are, to a variable extent, refilled by hydrothermal assemblages, including quartz, albite, K-feldspar, hematite, chlorite and calcite. The geometry and spatial distribution of episyenite argue against an extreme fluid/rock ratio and it is inferred that the fluids had at least a moderate salinity with a temperature in excess of 300 °C. The dissolution process was

  18. Partitioning of F Between Aqueous Fluids and Albite Granite Melt and Its Petrogenetic and Metallogenetic SignifiCance

    Institute of Scientific and Technical Information of China (English)

    熊小林; 朱金初; 等


    The fluid/melt partitioning experiments on fluorine were carried out in the system albite-H2O-HF at P=100MPa,770℃≤T≤800℃and wt 2%-6% conditions.The concentrations of fluorine in quenched glasses(melt) were determined by electron microprobe and those of flusorine in the coexisting aqueous fluid were calculated by the method of mass balance The result shows that the fluorine was concentrated in graniteic melt relative to the coexisting fluid.The partition coefficient DF(wtFF1/wtFMt)ranges from 0.35to 0.89,It increases with increasing fluorine content in the system,this means that there is not just one single value of partition coefficicent for fluorine in the granitic melt-fluid system.The partitioning behavior of fluorine in this system depends critically on fluorine and proton(H+) concentrations.Our data suggest that F-rich granitic melts exist in nature and that fluorine may not be an important complexing agent of metal elements in F-bearing fluids.

  19. First-principles investigation of equilibrium isotopic fractionation of Si and O isotopes among quartz, albite, anthorite, orthoenstatite, clinoenstatite, olivine, and zircon (United States)

    Qin, T.; Wu, F.; Huang, F.; Wu, Z.


    Silicon is one of the most abundant elements in the crust and mantle. Because of advance of high precision analytical technique, Si isotope geochemistry has been widely applied into studies of a variety of important processes including planetary formation, core-mantle segregation, magmatism, and weathering of the crust. In order to better understanding Si isotope data in high temperature rock and mineral samples, it is critical to obtain equilibrium fractionation factors of Si isotopes among silicate minerals. However, experimental studies on calibrating Si isotope fractionation factors are still no available in literature. Here we used first-principles calculation based on density functional theory to investigate Si isotope fractionation factors among silicate minerals commonly occurring in magmatism in crustal level. These minerals include quartz, albite, anthorite, orthoenstatite, clinoenstatite, olivine, and zircon. We also calculated oxygen isotope fractionation factors among these minerals. Our results indicate the 18O-enrichment order among these minerals follows sequence of quartz > albite > anorthite > enstatite> zircon > olivine, showing good agreement with the data from previous experiments or natural sample measurement. For Si isotopes, our work shows that the 30Si-enrichment order in these minerals follows sequence of quartz > albite > anorthite > olivine ~ zircon > enstatite > diopside. These results are consistent with previous calculation [1] and observation from natural minerals. For example, Δ30Sianorthite-olivine = 0.2‰ at 1000oC based on our calculation, well consistent with value from the study of Skaergaard Intrusion (Δ30Siplagioclase-olivine = 0.24-27‰) [2] at same temperature. Our calculation indicates that Si isotopes can be significantly fractionated among silicate minerals during high temperature geochemical processes. References: [1] M. Méheut et al (2007), GCA 71:3170-3180. [2] P. S. Savage et al (2011), GCA 75:6124-6139.

  20. Micro-area Chemical Composition and Preserved P-T Evolution Trace of Phengite in Albite Gneiss from the Donghai Ultrahigh-Pressure Metamorphic Area, East China

    Institute of Scientific and Technical Information of China (English)


    Study of micro-area chemical compositions indicates that phengite in albite gneiss from hole ZK2304 of the Donghai region has evident compositional zoning. SiO2 and tetrahedrally coordinated Si contents decrease, and Al2O3, AlIV and AlVI contents increase gradually from core to rim. However, K2O, MgO and FeO contents basically remain unchanged from core to rim. According to P-T estimates obtained from geothermometers and barometers, combined with previous experimental data, the core belt (micro-area I) of phengite was formed at T=637- 672° C and P=1.55- 1.73 GPa, and the transitional belt (micro-area II) of the phengite were formed at T=594- 654° C and P=1.35- 1.45 GPa. Towards the rim belt (micro-area III), the temperature decreased slightly, but the pressure decreased rapidly with T=542- 630° C and P=1.12- 1.19 GPa. The P-T evolution path recorded by the compositional zoning of phengite is characterized by significant near-isothermal decompression, revealing that the gneiss has undergone high-pressure-ultrahigh-pressure metamorphism. The compositional zoning of the phengite in the albite gneiss may have formed in the geodynamic process of rapid exhumation in the Sulu ultrahigh-pressure metamorphic belt.

  1. Albitization and hydrothermal diagenesis of Yanchang oil sandstone reservoir,Ordos Basin%鄂尔多斯盆地三叠系延长组砂岩钠长石化与热液成岩作用研究

    Institute of Scientific and Technical Information of China (English)

    李荣西; 段立志; 陈宝赟; 夏冰; 李靖波


    鄂尔多斯盆地延长组储层砂岩发育大量自生钠长石矿物,其成因和产出与浊沸石有关,含量和分布比浊沸石多而广泛,但没有引起人们的注意.大量详细岩相学观察发现延长组储层砂岩发育丰富的自生钠长石,其主要为由斜长石碎屑蚀变形成或呈胶结物充填分布在砂岩碎屑颗粒之间.钠长石中含有大量原生的发亮黄色荧光的油气包裹体,表明其形成与油气注入同时.电子探针成分分析表明,钠长石Na2O含量较高,几乎为斜长石的纯钠长石端员(NaAlSi3O8),没有钙长石端员(CaAl2Si2O8).激光拉曼光谱特征反映出钠长石为沉积成岩期形成的低温钠长石,而非来源于岩浆岩或者变质岩区的碎屑钠长石.应用LA-MC-ICP/MS原位微分析技术对钠长石进行的稀土元素分析表明,延长组砂岩钠长石具有热水成岩作用地球化学特征,属于热液成岩作用产物.认为大量钠长石形成与石油充注的同时进行导致了储层致密过程中岩性油藏的形成.延长组储层砂岩中热液成岩作用对油藏形成和分布意义重大,值得重视和研究.%The Triassic low permeability reservoir sandstone of Yanchang Formation in Ordos Basin is composed of fine-grained arkose and feldspathic litharenite. Lots of research work has been devoted to the diagenesis of reservoir sandstone of Yanchang Formation. It is considered that the formation of secondary pore through dissolution of laumontite improved the reservoir property of sandstone, and the dissolution of laumontite was closely related to alteration of plagioclase. According to the equilibrium theory of mineral reaction, the laumontite formed by the alteration of plagioclase accompanied by the formation of albite is two times as many as the laumontite in quantity. Therefore, if laumontite of sandstone in Yanchang Formation was dissolved to form dissolution pores, the content of albite with more stability should be higher in theory

  2. Hydrothermal Alteration Zoning and Kinetic Process of Mineral-Water Interactions

    Institute of Scientific and Technical Information of China (English)

    张荣华; 胡书敏; 苏艳丰


    This study reports the kinetic experimental results of albite in water and in KCl solution at 22 MPa in the temperature range of 25 to 400(C. Kinetic experiments have been carried out in an open flow-through reaction system (packed bed reactor). Albite dissolution is always incongruent in water at most temperatures, but becomes congruent at 300(C (close to the critical point 374(C). At temperatures from 25 to 300(C, the incongruent dissolution of albite is reflected by the fact that sodium and aluminum are easily dissolved into water; from 300 to 400(C it is reflected by silicon being more easily dissolved in water than Al and Na. Maximum albite dissolution rates in the flow hydrothermal systems have been repeatedly observed at 300(C, independent of flow rates.The kinetic experiments of albite dissolution in a KCl aqueous solution (0.1 mol KCl) indicate that the dissolution rate of albite increases with increasing temperature. Maximum silicon release rates of albite have been observed at 400(C, while maximum aluminum release rates of albite at 374(C. The reaction rates of albite also depend on the potassium concentration in the aqueous solution.These results can be used to interpret the mechanism for forming hydrothermal alteration. The kinetic experiments of mineral-aqueous solutions interactions in the hydrothermal system from 25 to 400(C and at 22 MPa indicate that the formation of the feldspar-mica-kaolinite zoning occurring in some ore deposits may depend not only on the mineral stability but also on the kinetics of feldspar hydration, which is affected by the water property variation when crossing the critical point.

  3. Thermo-optical properties of optically stimulated luminescence in feldspars

    DEFF Research Database (Denmark)

    Poolton, N.R.J.; Bøtter-Jensen, L.; Johnsen, O.


    Optically stimulated luminescence processes in feldspars are subject to competing thermal enhancement and quenching processes: this article describes the thermal enhancement effects for orthoclase, albite and plagioclase feldspars. It is demonstrated that certain lattice vibrational modes can be ...

  4. Kinetics of Hydrothermal Reactions of Minerals in Near-critical and Supercritical Water

    Institute of Scientific and Technical Information of China (English)


    This work presents new experimental results on the kinetics of mineral dissolution in near-critical and supercritical water in a temperature range (T) from 25 to 400° C and a constant pressure of 23 MPa. Kinetic experiments were carried out by using a flow reactor (packed bed reactor) of an open system. The dissolution rates of albite and magnetite were measured under these experimental conditions. Na, Al and Si release rates for albite dissolution in water were measured as a function of the temperature and flow velocity in the reaction system. The maximum release rates of Na, Al and Si of albite dissolution in the hydrothermal flow systems under different flow velocities were always obtained at 300° C, that is to say, the maximum albite dissolution rates in the flow systems, regardless of different flow rates, were repeatedly measured at 300° C. Results indicate a wide fluctuation in albite dissolution rates occurring close to the critical point of water. The dissolution rates increased when the temperatures increased from 25 to 300° C and decreased when the temperatures increase from 300 to 400° C. At some flow velocities, the dissolution rates rose as the temperature surpassed 374° C. Albite dissolution was incongruent in water at most temperatures. It was only at 300° C that albite dissolution was congruent. The albite dissolution from 25 to 300° C (at 23 MPa) will change from incongruent to congruent, whereas from subcritical 300 to 400° C (at 23 MPa), the dissolution will change from congruent to incongruent. The release ratio of Al/Si (or Na/Si) is positive at T300° C. The dissolution rates of magnetite in water increased with increasing T until T at the critical point of water or around it. The authors believe that this is caused by the wide fluctuations in water properties under the conditions from the near-critical to supercritical state.

  5. Sodium storage in deep paleoweathering profiles beneath the Paleozoic-Triassic unconformity (United States)

    Thiry, M.; Parcerisa, D.; Ricordel-Prognon, C.; Schmitt, J.-M.


    A major sodium accumulation has been recognized for long and by numerous authors in the Permo-Triassic salt deposits (Hay et al., 2006). Beside these basinal deposits, important masses of sodium were stored on the continents within deep palaeoweathering profiles in form of albite. Indeed, wide surfaces and huge volumes of granito-gneissic basements of the Hercynian massifs are albitized from North-Africa up to Scandinavia. These albitized rocks have usually been considered as related to tardi-magmatic metasomatic processes (Cathelineau 1986; Petersson and Eliasson 1997). Geometrical arrangement and dating of these alterations point out that these albitizations, or at least a part of them, developed under low temperature subsurface conditions in relation with the Triassic palaeosurface (Ricordel et al., 2007; Parcerisa et al., 2009). Petrology The albitized igneous rocks show a strong alteration with pseudomorphic replacement of the primary plagioclases into albite, replacement of primary biotite by chlorite and minor precipitation of neogenic minerals like albite, chlorite, apatite, haematite, calcite and titanite. Albitized rocks are characterized by their pink coloration due to the presence of minute haematite inclusions in the albite. The development and distribution of the albitization and related alterations above the unaltered basement occurs in three steps that define a vertical profile, up to 100-150 m depth. 1) In the lower part of the profile, albitization occurs within pink-colored patches in the unaltered rock, giving a pink-spotted aspect to the rock. 2) In the middle part of the profile, rocks have an overall pink coloration due to the albitization of the primary Ca-bearing igneous plagioclases. Usually, this facies develops in a pervasive manner, affecting the whole rock, but it may also be restricted to joints, giving a sharp-pink coloration to the fracture wall. 3) Finally, the top of the profile is defined by the same mineral paragenesis as in the

  6. Glide twinning and pseudotwinning in peristerite: twin morphology and propagation (United States)

    Brown, William L.


    Optically visible Albite glide “twins” in a peristerite (˜An9Or1.6), identified from their tapering shape and relationship to grain boundaries, were studied by transmission electron microscopy. Near the tips in sections ⊥ a, the microstructure consists of small (˜400 nm long) lensshaped Albite twins centred exclusively on the oligoclase lamellae. The lenses extend partly outwards into the two adjacent low albite lamellae and induce strong inhomogeneous strain. Where the lenses are closer together, they form, depending on the sense of shear, nearly linear left or right-stepping en échelon arrays, with overlap of the strain fields. Slightly farther in from the tip, the twin domains coalesce to form continuous pinch-and-swell lamellae, being always thicker in the oligoclase. Because of Si,Al order, only elastic glide pseudotwins are possible in low albite. In oligoclase glide pseudotwins may be mechanically stable (metastable relative to Si,Al order) and may deviate only slightly from true twins. Pseudotwins develop first in the oligoclase, propagate dynamically by jumping across the intervening albite lamellae, extend lengthways and thicken sideways and finally coalesce. They are stabilized by diffusion-controlled inversion of Si,Al order giving rise to true twins described in a companion paper.

  7. Multiple Feldspar replacement in Hercynian granites of the Montseny-Guilleries Massif (Catalan Coastal Ranges, NE Spain) (United States)

    Fàbrega, Carles; Parcerisa, David; Gómez-Gras, David


    The core of the Montseny-Guilleries Massif (Catalan Coastal Ranges) is mainly composed by late-Hercynian granitoids (leucogranites and granodiorites) intruded within Cambrian to Carnoniferous metasediments. The granites are unconformably covered by Triassic (Buntsandstein) and Paleocene red beds at the western boundary, preserving a continuous outcrop of the Permo-Triassic unconformity for about 20 km. In the southwestern Montseny-Guilleries Massif the granites are covered by the Buntsandstein red sandstones that overlain a peneplain paleorelief called the Permo-Triassic palaeosurface. Beneath the palaeosurface the granite displays a characteristic pink colouration. This pink alteration is characterized by precipitation of minute heamatite crystals and albitization of pristine plagioclases (mostly labradorite). The secondary albite is pseudomorphic (mono- or polycrystalline), optically continuous, non-luminiscent, contains widespread microporosity and displays compositions about Ab98. These features are typical of low temperature replacive feldspars (Kastner and Siever, 1979). Albitization of plagioclases is almost total close to the Permo-Triassic palaeosurface and progressively decreases towards depth, displaying a 150-200 m thick alteration profile. The formation of this profile was controlled by fluid circulation along macro- and microfractures and crystal boundaries. Inside the plagioclase crystals fluid pathways were microfractures, twinning and cleavage planes and crystalline defects. The secondary albite holds widespread unconnected micron-size porosity often filled by Fe-oxides. The reaction front is sharp and displays an abrupt composicional change (Ab65 to Ab98) at micron scale. Porosity only appears to be connected at this reaction front surface. The geometrical arrangement of this alterations suggest that albitization was a shallow process related with Na-rich descending fluids linked to the Permo-Triassic palaeosurface, in a similar way to

  8. Integration of geophysical and geological data for delimitation of mineralized zones in Um Naggat area, Central Eastern Desert, Egypt

    Directory of Open Access Journals (Sweden)

    Ibrahim Gaafar


    Interpretations of the aeromagnetic maps delineated four regional structural trends oriented due NNW, NW, ENE and E–W directions. They are identified as strike-slip faults, which coincide well with field observations, where NW-trending faults cut and displace right laterally ENE-trending older ones. The interaction between these two strike-slip fault systems confining the albite granite is easily identified on the regional data presenting longer wavelength anomalies, implying deep-seated structures. They could represent potential pathways for migration of enriched mineralized fluids. Geochemically, albite granites of peraluminous characteristics that had suffered extensive post-magmatic metasomatic reworking, resulted into development of (Zr, Hf, Nb, Ta, U, Th, Sn and albite-enriched and greisenized granite body of about 600 m thick, and more than 3 km in strike length. The albite granite is characterized by sharp increase in average rare metal content: Zr (830 ppm, Hf (51 ppm, Nb (340 ppm, Ta (44 ppm, and U (90 ppm. Thorite, uranothorite, uraninite and zircon are the main uranium-bearing minerals of magmatic origin within the enclosing granite. However, with respect to Zr, Nb, and Ta, the albitized granite can be categorized as rare metal granite. The integration of airborne geophysical (magnetic and γ-ray spectrometric, geological, geochemical and mineralogical data succeeded in assigning the albite granite of Um Naggat pluton as a mineralized zone. This zone is characterized by its high thorium and uranium of hydrothermal origin as indicated by its low Th/U ratio, with rare metals mineralization controlled by two main structural trends in the NW- and ENE-directions.

  9. An occurrence of metastable cristobalite in high-pressure garnet Granulite (United States)

    Darling, R.S.; Chou, I.-Ming; Bodnar, R.J.


    High-pressure (0.8 gigapascals) granulite facies garnet from Gore Mountain, New York, hosts multiple solid inclusions containing the low- pressure silica polymorph cristobalite along with albite and minor ilmenite. Identification of cristobalite is based on Raman spectra, electron microprobe analysis, and microthermometric measurements on the ??/?? phase transformation. The cristobalite plus albite inclusions may have originated as small, trapped samples of hydrous sodium-aluminum-siliceous melt. Diffusive loss of water from these inclusions under isothermal, isochoric conditions may have resulted in a large enough internal pressure decrease to promote the metastable crystallization of cristobalite.

  10. An Occurrence of Metastable Cristobalite in High-Pressure Garnet Granulite (United States)

    Darling; Chou; Bodnar


    High-pressure (0.8 gigapascals) granulite facies garnet from Gore Mountain, New York, hosts multiple solid inclusions containing the low-pressure silica polymorph cristobalite along with albite and minor ilmenite. Identification of cristobalite is based on Raman spectra, electron microprobe analysis, and microthermometric measurements on the alpha/beta phase transformation. The cristobalite plus albite inclusions may have originated as small, trapped samples of hydrous sodium-aluminum-siliceous melt. Diffusive loss of water from these inclusions under isothermal, isochoric conditions may have resulted in a large enough internal pressure decrease to promote the metastable crystallization of cristobalite.

  11. U–Pb zircon and biostratigraphic data of high‐pressure/ low‐temperature metamorphic rocks of the Talea Ori : tracking the Paleotethys suture in central Crete, Greece

    NARCIS (Netherlands)

    Zulauf, G.; Dörr, W.; Krahl, J.; Lahaye, Y.; Chatzaras, V.; Xypolias, P.


    Inherited deformation microfabrics of detrital quartz grains and U–Pb (Laser ablation (LA)-ICPMS and ID TIMS) ages of detrital zircons separated from the Phyllite–Quartzite Unit s.l. of the Talea Ori, central Crete, suggest strikingly different source rocks. Albite gneiss of the lower Rogdia Beds in

  12. Evaluation of Geothermal Potential of Range Bravo 17 and the Shoal Site, Naval Air Station, Fallon. (United States)


    is almost completely argillized and sericitized. The porphyritic rhyolite contains up to 30% phenocrysts of quartz, sani- dine, and/or albite in a...groundmass of the same minerals, plus 0.5% biotite. Some of the porphyritic rhyolite exhibits propylization, argillization , sericitization, and/or

  13. FT-IR and micro-Raman spectroscopic study of decorated potteries from VI and VII century BC, excavated in ancient Ainos Turkey (United States)

    Akyuz, S.; Akyuz, T.; Basaran, S.; Bolcal, C.; Gulec, A.


    Ancient decorated pottery fragments belong to sixth and seventh century BC, excavated in the archaeological district of Enez - Turkey (Ancient Ainos) were analysed using micro-Raman and FT-IR spectroscopy. The experimental results allowed us to identify the peculiar components of the ceramic body and the main pigments of the decoration. The presence of albite and anatase suggests low firing temperatures.

  14. Eudialyte decomposition minerals with new hitherto undescribed phases from the Ilímaussaq complex, South Greenland

    DEFF Research Database (Denmark)

    Karup-Møller, Sven; Rose-Hansen, J.; Sørensen, H.


    are distinguished: alteration of eudialyte to catapleiite is widespread in the complex, whereas alteration to zircon only occurs in strongly altered rocks. additionally, the fol-lowing minerals have been identified in the altered eudialyte: aegirine, K-feldspar, albite, analcime, fluorite, monazite, apatite...

  15. Geochemical characteristics and spectrometric prospecting in the muscovite-bearing pegmatites and granites, southeastern Aswan, Egypt

    Institute of Scientific and Technical Information of China (English)

    Gehad M. Saleh; Mohamed M. El Galy; Mohamed A. Obeid


    Rare metal mineralization of Sn, Nb-Ta and W is encountered in the Gebel Dihmit area (GDA), southeastern Aswan, Egypt. The mineralization is related to muscovite granites and their pegmatite derivatives. The pegmatites are divided into three types according to their main mineral assemblages: K-feldspar-muscovite-tourmaline, K-feldspar-albite-muscovite and albite-K-feldspar-lepidolite veins. Petrogenetic studies indicate that Sn and Nb-Ta mineralization extends from the late-magmatic stage to the pegmatite and hydrothermal stages of the (GDA) suite. The albite-K-feldspar-lepidolite granite is composed dominantly of albite, lepidolote, and quartz, with topaz, K-feldspar and amblygonite. The accessory minerals are zircon, monazite, pollucite, columbite-tantalite, microlite and Ta-rich cassiterite. Phenocrysts of quartz, topaz and K-feldspar contain abundant inclusions of albite laths and occasional lepidolite crystals along growth zones (snowball texture), indicating simultaneous crystallization from a subsolvus, residual magma. The origin of the pegmatites is attributed to extreme differentiation by fractional crystallization of a granitic magma. The economic potential for rare metals was evaluated in the geochemical discrimination diagrams. Accordingly, some of the pegmatites are not only highly differentiated in terms of alkalis, but also the promising targets for small-scale Ta and, to a less extent, Sn. The pegmatites also provide the first example of Fe-Mn and Nb-Ta fractionation in successive generations of granites to cassiterite-bearing pegmatites, which perfectly exhibit similar fractionation trends established for primary columbite-tantalite in the corresponding categories of pegmatites. Uranium and Th of magmatic origin are indicated by the presence of thorite and allanite, whereas evidence of hydrothermal mineralization is the alteration of rock- foring minerals such as feldspar and the formation of secondary minerals such as uranophane..

  16. Kinetic Modeling of Diagenesis of Eogene Lacustrine Sandstone Reservoirs in the Jianghan Basin, Southeastern China

    Institute of Scientific and Technical Information of China (English)

    倪师军; 卿海若; 唐建武; 周美夫; 李泽琴


    In the Tuoshi oilfield, located in the Cenozoic Jianghan Basin of southeastern China, there have been found hydrocarbon reservoirs hosted in lacustrine sandstones of the Eogene Xingouzui Formation. The main diagenetic features identified in these sandstones include the dissolution of detrital K-feldspar and albite grains, the precipitation of quartz as overgrowths and/or cements, and the precipitation and/or transformation of clay minerals. These diagenetic features were interpreted to have occurred in early, intermediate and late stages, based on the burial depth. The kinetics of fluid-mineral reactions and the concentrations of aqueous species at each stage of diagenesis were simulated numerically for these lacustrine sandstones, using a quasi-stationary state approximation that incorporates simultaneous chemical reactions in a time-space continuum. During the early diagenetic stage, pore fluid was weakly acidic, which resulted in dissolution of K-feldspar and albite and, therefore, led to the release of K + , Na + , Al3 + and SiO2(aq) into the diagenetic fluid. The increased K+ , Na + , Al3+ and SiO2(aq) concentrations in the diagenetic fluid caused the precipitation of quartz, kaolinite and illite. At the beginning of the intermediate diagenetic stage the concentration of H + was built up due to the decomposition of organic matter, which was responsible for further dissolution of K-feldspar and albite and precipitation of quartz, kaolinite, and illite. During the late diagenetic stage, the pore fluid was weakly alkaline, K-feldspar became stable and was precipitated with quartz and clay minerals.When the burial depth was greater than 3000 m, the pore fluids became supersaturated with respect to albite, but undersaturated with respect to quartz, resulting in the precipitation of albite and the dissolution of quartz. The diagenetic reactions forecasted in the numerical modeling closely matched the diagenetic features identified by petrographic examination, and

  17. Origin of alternate amphibole and quartz rich bands in amphibole bearing quartzite from North Khetri Copper Belt, Rajasthan, India (United States)

    Paul, J.; Baidya, A. S.; Pal, D. D. C.


    North Khetri Copper Belt (NKCB), located in the northern part of Western Indian shield, is one of most important copper repositories in India. Mineralization is hosted by quartzite containing abundant amphibole in the form of alternation of amphibole ± albite and quartz ± albite bands. In a succession near Chandmari mine of NKCB, this thick banded unit is laterally extended over few hundreds of meters. Band thickness varies from few millimetres to tens of centimetres. Such banding (commonly appearing as gneissic banding) of amphibole ± albite is unlikely to be generated in a quartzo-feldspathic rock metamorphosed at lower amphibolite facies. Amphibole, under microscope, shows pleochroism in shades of green. Their grains are inclusion free and do not show any orientation. From major oxide analysis, their average composition is found to be Ca2Mg2.5Fe2+1.5Fe3+0.5Al1.5Si7O22(OH)2. Forming Fe-Mg rich amphibole in a quartzo-feldspathic unit is again challenging its metamorphic origin. Also, amphibole of same composition found in the form of veins within the host rock. All these observations inferring that the amphibole is probably of hydrothermal origin. Albite in host rock can supply Si, Al and O. If a fluid containing Fe, Mg and Ca intrudes into the host rock, the amphibole of desirable composition may form. However, such alternating banding of amphibole ± albite and quartz ± albite is enigmatic. It is possible that the banded nature is inherited from an existing banded rock with different mineralogy and mineral solubility, e.g. alternation of impure/siliceous carbonate and siliciclastic rocks. Presence of carbonate, mainly dolomite, has been reported early and also observed in field. When a hydrothermal fluid, containing some Fe, had invaded this unit, it reacted with carbonate units and replaced the carbonate by amphibole. This will result in amphibole of expected composition and will also mimic the inherited banded nature in original succession. Reaction will

  18. The Durulgui rare-metal granite‒pegmatite system in the eastern Transbaikal region: Petrological and geochronological aspects (United States)

    Zagorsky, V. E.


    The Durulgui granite‒pegmatite system unites the Dedova Gora granite massif and pegmatite field with the Chalotskoe beryl deposit. New geochronological data on micas from porphyric biotite granites, fine-grained biotite granites, two-mica granites, and Be-bearing pegmatites are discussed. The plateau age of 128.5(±1.5)-131.2(±1.5) should be considered as indicating the formation time of the granite‒pegmatite system as a whole. The age of the system implies the possibility of its formation owing to several magmatic pulses. This assumption concerns porphyric and fine-grained biotite granites and two-mica and muscovite granites, the contact between which is locally sharp. At the same time, the succession "two-mica granites → muscovite granites → granite‒pegmatites → microcline pegmatites → microcline‒albite pegmatites → albite pegmatites" demonstrates gradual facies transitions between rocks, which indicates their emplacement during a single magmatic pulse.

  19. Investigation of the mineral components of porcelain raw material and their phase evolution during a firing process by using a Rietveld quantitative analysis (United States)

    Kim, Jaegyeom; Heo, Eunae; Kim, Seung-Joo; Kim, Jong-Young


    A ceramic raw material for white porcelain and its phase evolution during a firing process were investigated by using Rietveld method based on powder X-ray diffraction data. The raw material was mainly composed of five mineral phases: quartz (SiO2), microcline (KAlSi3O8), albite (NaAlSi3O8), muscovite (KAl2(AlSi3O10)(OH)2), and kaolinite (Al2Si2O5(OH)4). The amount of each mineral phase could be determined by using Rietveld quantitative phase analyses. During the firing process, the microcline, albite, muscovite and kaolinite phases started to react with each other to produce the mullite phase embedded in an amorphous matrix. The amount of quartz remained nearly unchanged until a temperature above 1200 °C; then, it converted to an amorphous phase at higher temperatures.

  20. Structural controls and evolution of gold-, silver-, and REE-bearing copper-cobalt ore deposits, Blackbird district, east-central Idaho: Epigenetic origins (United States)

    Lund, K.; Tysdal, R.G.; Evans, K.V.; Kunk, M.J.; Pillers, R.M.


    The Cu-Co ± Au (± Ag ± Ni ± REE) ore deposits of the Blackbird district, east-central Idaho, have previously been classified as Besshi-type VMS, sedex, and IOCG deposits within an intact stratigraphic section. New studies indicate that, across the district, mineralization was introduced into the country rocks as a series of structurally controlled vein and alteration systems. Quartz-rich and biotite-rich veins (and alteration zones) and minor albite and siderite veinlets maintain consistent order and sulfide mineral associations across the district. Both early and late quartz veins contain chalcopyrite and pyrite, whereas intermediate-stage tourmaline-biotite veins host the cobaltite. Barren early and late albite and late carbonate (generally siderite) form veins or are included in the quartz veins. REE minerals, principally monazite, allanite, and xenotime, are associated with both tourmaline-biotite and late quartz veins. The veins are in mineralized intervals along axial planar cleavage, intrafolial foliation, and shears.

  1. Geochemistry of the Late Neoproterozoic Hadb adh Dayheen ring complex, Central Arabian Shield: Implications for the origin of rare-metal-bearing post-orogenic A-type granites (United States)

    Moghazi, A. M.; Harbi, H. M.; Ali, K. A.


    The Hadb adh Dayheen ring complex (HDRC), Central Arabian Shield, is an alkaline to peralkaline A-type granite complex. It consists of an inner core of monzogranite followed outward by porphyritic alkali feldspar granite (hornblende biotite granite and aegirine riebeckite granite). Field and textural observations indicate that the different granite types were separated from magma reservoir, at different stages, and emplaced at higher levels along pre-existing fractures. The geochemical characteristics indicate that their magma was most plausibly originated by partial melting of juvenile lower crust following collision between East and West Gondwana at the final stage of the Arabian Shield evolution. The alkali feldspar granites have high abundances of albite and fluorite and wide variation of HFSE and REE that indicate interaction with hydrothermal F-rich fluids. Although there are many geochemical, mineralogical and textural evidence of secondary metasomatic alteration superimposed on the granitic rocks, they show textural features such as the arrangement of albite inclusions along growth planes in quartz (snowball texture) and aegirine that indicate early magmatic crystallization of albite. Also, the strong linear positive correlation of Ta vs. Nb and Zr vs. Hf emphasize that the behavior and enrichment of Ta and Nb are largely controlled by magmatic processes. The events that can explain the evolution of these rocks are: (1) during magmatic evolution, F dissolved in the magma and lowered the crystallization temperature causing REE and HFSE to form complexes and thus behave as incompatible elements, (2) prolonged crystallization of the major mineral phases (quartz and feldspar) formed a late-stage magmatic fluid enriched in volatiles (H 2O, F) and trace elements, (3) accessory minerals crystallized from such a phase in the interstices between the major mineral phases, and (4) post-magmatic re-equilibration and formation of secondary albite (Na-metasomatism) has

  2. A-thermal elastic behavior of silicate glasses. (United States)

    Rabia, Mohammed Kamel; Degioanni, Simon; Martinet, Christine; Le Brusq, Jacques; Champagnon, Bernard; Vouagner, Dominique


    Depending on the composition of silicate glasses, their elastic moduli can increase or decrease as function of the temperature. Studying the Brillouin frequency shift of these glasses versus temperature allows the a-thermal composition corresponding to an intermediate glass to be determined. In an intermediate glass, the elastic moduli are independent of the temperature over a large temperature range. For sodium alumino-silicate glasses, the a-thermal composition is close to the albite glass (NaAlSi3O8). The structural origin of this property is studied by in situ high temperature Raman scattering. The structure of the intermediate albite glass and of silica are compared at different temperatures between room temperature and 600 °C. When the temperature increases, it is shown that the high frequency shift of the main band at 440 cm(-1) in silica is a consequence of the cristobalite-like alpha-beta transformation of 6-membered rings. This effect is stronger in silica than bond elongation (anharmonic effects). As a consequence, the elastic moduli of silica increase as the temperature increases. In the albite glass, the substitution of 25% of Si(4+) ions by Al(3+) and Na(+) ions decreases the proportion of SiO2 6-membered rings responsible for the silica anomaly. The effects of the silica anomaly balance the anharmonicity in albite glass and give rise to an intermediate a-thermal glass. Different networks, formers or modifiers, can be added to produce different a-thermal glasses with useful mechanical or chemical properties.

  3. Los sistemas geotermales del Pirineo Central. III. Evaluación de las condiciones en profundidad y evolución de las soluciones hidrotermales durante su ascenso


    Gimeno, M. J.; Lapuente, M. P.; López, P. L.; Mandado, J.; Auqué, L. F.


    Reservoir temperature and physicochemical conditions are determined by modelling the heating of alkaline waters in Caldas de Bohi, Arties, Luchon, Cauterets, Panticosa and Benasque geothermal systems (Central Pyrenees). Kaolinite reequilibrium occurs during the ascent of these thermal waters and therefore simulations are performed in open system conditions with kaolinite. Calculations indicate that thermal waters are in equilibrium with a common mineral assemblage constituted by albite, micro...

  4. 硅铍钠石在水热条件下的形成

    Institute of Scientific and Technical Information of China (English)



    Experiments on the formation of chkalovite through reactions of beryl with aqueous solutions of Na2B4O7-·10H2O, NaHCO8 and NaOH respectively were carried out under hydrothermal conditions. Comparison of mineralogical features was also made between chkalovites formed under different alkaline media mentioned above. The order of crystallization of coexisting minerals (albite, cancrinite, and analcite) is discussed and possible cbemical reactions involved in the formation of chkalovite suggested.

  5. Low-grade Prehnite-Pumpellyite facies metamorphism in the Bamble sector, SE-Norway


    Velo, Mari Roen


    Low-grade metamorphic minerals have been found within the high-grade terrain in the Bamble sector, SE-Norway. The minerals prehnite and pumpellyite indicative of prehnite-pumpellyite facies conditions have been confirmed around the Kragerø area. The formation of analcime, thomsonite, hydrogarnet, albite and clay minerals is also a part of the low-grade metamorphism. The occurrence of these low-grade minerals is constricted to pseudomorph replacement of earlier mineral phases, hydrothermal vei...

  6. Petrography and geochemical study of Nezam-Abad area, Southwest of Shazand, Arak


    Robabeh Jafari; Moosa Noghreeian; Mohammad Makizadeh


    Nezam-Abad area is located in southwest of Shazand (Arak) which is a part of Sanandaj-Sirjan zone. Major intrusive rocks of Nezam-Abad are quartz diorite and minor amount of granodiorite. Leucogranitic, pegmatite dykes and quartz-tourmaline veins were intruded the quartz diorite. Quartz diorites are mainly composed of plagioclase, hornblende, biotite, quartz and pyroxene as major minerals. Major minerals of leucogranite are microcline, orthoclase, albite, quartz, biotite and muscovite. Access...

  7. What is a twin structure? An answer from microcline minerals from pegmatites


    Sánchez Muñoz, Luis; Crespo Feo, Elena; García-Guinea, Javier; Moura, Odulio J. M. de; Zagorsky, Victor Ye.


    Twin-structures in microcline specimens from granite pegmatites were studied by polarized light microscopy (PLM) and Raman microprobe (RMP) spectra. Ordinary and diagonal Albite-Pericline orientation variants from transformation twinning (after a monoclinic precursor) and subsequent solid-state recrystallization twinning were observed. They exhibit a ¿complexity¿, related to the particular organizations of the twin units, that is totally expected from traditional crystallographic and equilibr...

  8. Mineral Surface after Reaction with Aqueous Solution at High Temperatures and Pressures

    Institute of Scientific and Technical Information of China (English)


    This work presents new experimental results on surface chemistry of reacting minerals and interface kinetics between mineral and aqueous solutions. These experiments were carried out using a flow reactor (packed bed reactor) of an open system as well as a continuous stirred tank reactor, CSTR. The authors measured reaction rates of such minerals as zeolite, albite and carbonate (rhodochrosite, dolomite) in various solutions, and tested corresponding mineral surface by using SEM, XPS, SIMS, etc. This paper mainly presents the experimental results of zeolite dissolution in water and in low pH solutions at room temperature, and dolomite dissolution at elevated temperatures. The results show that the release rates of Si, Al and Na of zeolite are different in most cases. The incongruent dissolution of zeolite is related to surface chemical modifications. The Na, Al and Si release rates for dissolution of albite and zeolite in water and various solutions were measured as a function of temperature, flow velocity, pH and solution composition in the reaction system. In most cases, dissolutions of both albite and zeolite are incongruent. Dissolution of dolomite is also incongruent in most cases and varied with T, pH, and nature of aqueous solutions. For dolomite dissolution, the release rates of Mg are less than those of Ca at high temperatures as T increases from 25 to 300° C. SIMS study indicates that the contents of Al, Na and Si in the leached layer of zeolite or albite surface, change with the distance from the surface, exhibiting a non-linear behaviour within a thickness range of 1000%. The distributions of Ca, Mg, Mn, H and Cl in the leached surface layer of carbonate have a non-linear behaviour too.

  9. Two modes of occurrence of garnets from the Tonaru metagabbro mass in the Sambagawa metamorphic belt, central Shikoku, Japan


    蔵谷, 樹; 高須, 晃; カビール, エムデイ ファズレー


    Garnet epidote amphibolite from the central part of the Tonaru metagabbro mass consists mainly of garnet, epidote and amphibole (ferro-hornblende), with small amounts of quartz, plagioclase (albite and oligoclase) and paragonite. Rutile, apatite, hematite, calcite and chlorite occur occasionally. Garnets in the garnet epidote amphibolites exhibit two modes of occurrence. Garnet 1 (Grt 1) occurs as porphyroblast, and garnet 2 (Grt 2) is found as fine grain in the matrix. Porphyroblastic garnet...

  10. Metasomatism of ferroan granites in the northern Aravalli orogen, NW India: geochemical and isotopic constraints, and its metallogenic significance (United States)

    Kaur, Parampreet; Chaudhri, Naveen; Hofmann, Albrecht W.; Raczek, Ingrid; Okrusch, Martin; Skora, Susanne; Koepke, Jürgen


    The late Palaeoproterozoic (1.72-1.70 Ga) ferroan granites of the Khetri complex, northern Aravalli orogen, NW India, were extensively metasomatised ~900 Ma after their emplacement, at around 850-830 Ma by low-temperature (ca. 400 °C) meteoric fluids that attained metamorphic character after exchanging oxygen with the surrounding metamorphic rocks. Albitisation is the dominant metasomatic process that was accompanied by Mg and Ca metasomatism. A two-stage metasomatic model is applicable to all the altered ferroan intrusives. The stage I is represented by a metasomatic reaction interface that developed as a result of transformation of the original microcline-oligoclase (An12-14) granite to microcline-albite (An1-3) granite, and this stage is rarely preserved. In contrast, the stage II metasomatic reaction front, where the microcline-bearing albite granite has been transformed to microcline-free albite granite, is readily recognisable in the field and present in most of the intrusives. Some of them lack an obvious reaction interface due to the presence of stage II albite granites only. When studied in isolation, these intrusives were incorrectly classified and their tectonic setting was misinterpreted. Furthermore, our results show that the mafic mineralogy of metasomatised granites has a significant impact on the characterisation of such rocks in the magmatic classification and discrimination diagrams. Nevertheless, the stage I metasomatised granites can be appropriately characterised in these diagrams, whereas the characterisation of the stage II granites will lead to erroneous interpretations. The close spatial association of these high heat producing ferroan granites with iron oxide-copper-gold (IOCG), U and REE mineralisation in the region indicates a genetic link between the metasomatism and the mineralisation. World-class IOCG, U and REE deposits are associated with metasomatised ferroan granites, suggesting that such a relationship may act as a critical

  11. Changes in the species composition of the rhizosphere and phyllosphere of sugar beet under the impact of biological preparations based on endophytic bacteria and their metabolites (United States)

    Pusenkova, L. I.; Il'yasova, E. Yu.; Lastochkina, O. V.; Maksimov, I. V.; Leonova, S. A.


    The species structure of the mycobiota in the rhizosphere and phyllosphere of sugar beet in ontogenesis was studied. The treatment of the plants with biopreparations based on endophytic bacteria and their metabolites (Phytosporin-M, Vitaplan, and Albit) were shown to create conditions for the colonization of the plant rhizosphere and phyllosphere by bacteria-antagonists displacing phytopathogenic microorganisms and stimulating plant growth, which induces the transformation of the microbial cenosis.

  12. Characterization of some clay deposits in South West Nigeria

    Directory of Open Access Journals (Sweden)

    Fatai Olufemi ARAMIDE


    Full Text Available Clay minerals are the most important industrial minerals whose application is dependent on its structure and chemical composition. Mineralogical, chemical compositions, phase constitutions, and microstructural morphology of certain clay minerals from three different deposits in south western Nigeria were investigated using state-of-the-art equipment. These were done with the intention of determining the appropriate application for the clay minerals. It was observed that the major phases in the clay samples from the three different deposits are kaolinite, microcline, muscovite/illite, plagioclase/albite and quartz. These phases were observed in varied percentages. It was concluded that sample A (Ifon clay which contains very low kaolinite (5.63%; could not use for making high temperature caliber refractories. But due to its high content of feldspar, it could be processed for the production of feldspar for glass and iron making industries. Sample B is considered to be appropriate for the production the refractory composite due to its most appropriate content of both kaolinite (23.74% kaolinite and feldspars (26.12% microcline and 11.28% plagioclase/albite which is necessary for producing mullite fibers in ceramic matrix at a temperature of around 1400oC. Sample C (Iseyin clay, which contains very low feldspars (3.00% microcline and 3.08% plagioclase/albite and high content of kaolinite was considered suitable for further processing for making high temperature caliber refractories.

  13. Clay mineralogy of the Boda Claystone Formation (Mecsek Mts., SW Hungary

    Directory of Open Access Journals (Sweden)

    Németh Tibor


    Full Text Available Boda Claystone Formation (BCF is the host rock of the planned site for high level nuclear waste repository inHungary. Samples representing the dominant rock types of BCF were studied: albitic claystone, claystone with high illite content, and analcime bearing claystone. Clay minerals in these three rock types were characterized by Xray powder diffraction (XRD, transmission electron microscopy (TEM and thermal analysis (DTA-TG, and the results were discussed from the point of view of the radionuclide sorption properties being studied in the future. Mineral compositions of bulk BCF samples vary in wide ranges. In the albitic sample, besides the dominant illite, few percent of chlorite represents the layer silicates in the clay fraction. Illite is the dominating phase in the illitic sample, with a few percent of chlorite. HRTEM study revealed that the thickness of illite particles rarely reaches 10 layers, usually are of 5-6 TOT layer thick. Illite crystals are generally thicker in the albitic sample than in the illitic one. The significant difference between the clay mineral characterisitics of the analcimous and the other two samples is that the former contains regularly interstratified chlorite/smectite beside the dominant illite.

  14. Influence of feldspar containing lithium in the sintering of triaxial ceramics; Sinterizacao de uma massa ceramica triaxial com feldspato contendo litio

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Camila Felippe de; Strecker, Kurt, E-mail: [Universidade Federal de Sao Joao del-Rei (UFSJ), MG (Brazil)


    In this work, the properties of a ceramic material based on a triaxial mass composed of clay, quartz and 15 to 30% feldspar, albite or spodumene, has been investigated. Specimen were prepared by uniaxial pressing under 28.5MPa and sintering at temperatures of 1000, 1100 and 1200 deg C, for 1h. The samples were characterized by their linear shrinkage, apparent porosity, apparent density and flexural strength, as well as analysis of the microstructure. The best results were obtained for samples prepared with 30% spodumene and sintered at 1200 deg C, with a shrinkage of 6.4%, density of 2.01g/cm{sup 3}, porosity of 14.3% and flexural strength of 13.4MPa, while samples prepared with albite exhibited shrinkage of 5.8%, density of 1.9g/cm{sup 3}, porosity of 18.9% and strength of 9.8MPa. Therefore, by the substitution of albite by spodumene in the ceramic triaxial mass, lower sintering temperatures may be employed, thus reducing production costs by the lesser energy consumption. (author)(.

  15. Experimental study on interaction between simulated sandstone and acidic fluid

    Institute of Scientific and Technical Information of China (English)

    Zhang Yongwang; Zeng Jianhu; Yu Bingsong


    In order to investigate the controlling mechanism of temperature, fluid and other factors on water-rock interaction in the diagenetic process, we performed a series of simulated experiments on the interaction between two kinds of fluids with different salinity and a composite mineral system (simulated sandstone), which contains albite, K-feldspar and other minerals. The experimental results showed that acidity was the most important factor that affected the dissolution of minerals in the composite mineral system. The lower the pH value, the more easily the minerals dissolved. At the same pH value, the dissolution abilities of different acids for various mineral components were also different. Compared to hydrochloric acid (inorganic acid), oxalic acid (organic acid) was more able to dissolve aluminosilicate minerals. However, the dissolution ability of oxalic acid for carbonate minerals was lower than that of hydrochloric acid. In the process of fluid-rock interaction,dissolution of feldspar was relatively complicated. Increase of temperature would accelerate the dissolution of feldspar. Under acidic conditions, albite had a higher dissolution rate than K-feldspar. K-feldspar could dissolve and convert into montmorillonite and kaolinite, while albite could dissolve and convert into kaolinite both at 40℃ and 80℃. Presence of organic acid, and decrease of pH value and water salinity were all favorable for the dissolution of feldspar, but weakened the ability to form clay minerals.

  16. Frictional Properties of Feldspar and Quartz at the Temperatures of Seismogenic Zone (United States)

    Arai, T.; Masuda, K.; Takahashi, M.; Fujimoto, K.; Shigematsu, N.; Sumii, T.; Okuyama, Y.


    Most of earthquakes in the crust occurred at the depth of 5 to 20km, and temperatures of 100 to 350° C. The physical properties of rocks at around these temperatures were determined by many frictional experiments. These results indicated the velocity dependence of steady state friction (a-b) was switched from velocity weakening ( seismic slip ) to velocity strengthening ( aseismic slip ) at around 350° C in the wet condition. In these experimental studies, granites were generally used. On the other hand, it is important to evaluate and to compare the physical properties of each mineral which composed of crustal rocks, for example feldspar and quartz, in order to understand the source processes of earthquakes in detail. In this study, we conducted frictional experiments by using albite, anorthite, and quartz gouges ( about 3μ m diameter ) under high pressure and high temperature in a triaxial apparatus, and compared frictional behaviors of three minerals with elevated temperature under the wet and dry conditions. These experiments were conducted by the velocity-stepping test. Temperature varied from room temperature to 600° C. In the dry conditions, experiments were conducted under the confining pressure of 150MPa. In the wet conditions, pore water pressure was applied up to 50MPa under the confining pressure of 200MPa. Sample was put between upper and lower sawcut alumina cylinders ( 20mm diameter x 40mm long ). The sawcut was oriented at 30° to the loading axis. These were jacketed with thin sleeves of annealed Cu. The values for a-b of quartz and albite were positive under the dry condition from room temperature to 600° C. On the other hand, those values of albite and quartz were negative at the temperature of 200° C and 300° C under the wet condition respectively. Those values of quartz decreased as the temperature increased from 100° C to 300° C and increased as the temperature increased from 300° C to 600° C. Those values of albite were switched

  17. Low magnification EBSD mapping of texture distribution in a fine-grained matrix (United States)

    Gardner, Joseph; Mariani, Elisabetta; Wheeler, John


    The study of texture (CPO) in rocks is often restricted to individual phases within a given sample or specific area of said sample. Large scale EBSD mapping of the matrix of a greenschist facies albite mylonite has shown that an overall significant CPO within albite grains is strongly domainal, and each domain has a unique CPO that is independent of both common slip systems in plagioclase and the specimen geometry (i.e. foliation and lineation). Observational evidence suggests the metamorphic breakdown of plagioclase to albite (Ab) plus a Ca-bearing phase (clinozoisite, Cz) has produced a two phase mixture in which each phase has a contrasting solubility. New grains of albite are thought to nucleate epitaxially from original plagioclase as a reaction front passes through parent grains. A pseudomorphic region of Ab plus Cz after an original plagioclase crystal, protected from intense deformation by enclosure in a cm-scale augite clast, gives insight into pre-deformation daughter grain distributions. The albite in the region inherits a strong CPO and 180° misorientation peak from a relict twin pattern due to epitaxial growth while clinozoisite is randomly distributed and oriented (despite some grains nucleating from the plagioclase parent twin boundary). In the deformed matrix, daughter Ab is seen to be the more mobile phase, having undergone obvious dissolution, transport and reprecipitation into fractures and pressure shadows, whereas Cz grains are relatively insoluble and rotate into parallelism with the foliation, forming bands that anastamose around Cpx porphyroclasts. Despite this modification, albite in the matrix retains significant CPOs that comprise distinct domains with sharp boundaries. A 180° misorientation peak thought to be a signature of twinning inherited from parent plagioclase is also observed in each domain. Why a CPO should be preserved under these conditions (contrary to our traditional understanding that CPOs are a signature of dislocation

  18. Origen de arcillas alumínicas en horizontes de alteración de materiales graníticos del borde sur de la sierra de Guadarrama

    Directory of Open Access Journals (Sweden)

    Martín Patino, M. T.


    Full Text Available Three weathering profiles of granitic rocks and two arkoses in the NW of Madrid Province have been studied. Rocks are granodiorites and adamellites with albites showing variable degrees of sericitization, and no-weathered potassic feldspars. Clay fraction in the weathered horizons from these rocks displays high content in beidellite, and minor amounts of illite and 7 Ǻ-halloysite. On the other hand, beidellite, illite and well crystallized kaolinite are clay minerals in the arkosic rocks. Microfabric characteristics from SEM studies show abundant weathered albites with clean surfaces and formation of beidellite in all areas of the samples. Moreover, spatial relations between albite and beidellite are not observed. In pedochemical weathering of albite, sodium from this mineral should be exchanged with protons from soil solution with very quick kinetics. This initial alkalinization produces an increase in the silica solubility released from albite network. In these environments, a continued contact between weathering solution and albite causes a silica and alumina enrichment and beidellite or 7 Ǻ-halloysite precipitation. Microclimatic variations in weathering environment may cause fluctuations in silica and alumina activities with resultant pH changes. So, when silica activities are high, beidellite neoformation is favoured; on the contrary, 7 Ǻ-halloysite is precipitated.Se han estudiado tres perfiles de alteración de rocas graníticas y dos muestras de arcosas en la zona NO de la provincia de Madrid. Las rocas, clasificadas como granodioritas y adamellitas, presentan albitas con sericitización variable, y escasos feldespatos potásicos muy poco alterados. La fracción arcilla de los horizontes de alteración de estas rocas presenta un alto contenido en beidellita, así como porcentajes menores de ilita y haloisita-7Ǻ. Por otra parte, los minerales de la arcilla presentes en las arcosas son ilita, beidellita y caolinita bien

  19. Geochemical and Mineralogical Characteristics of Pleistocene Lignites and Associated Sediments of Marathousa Coal Field,Central Peloponnese,Greece

    Institute of Scientific and Technical Information of China (English)



    The mineralogy and geochemistry data are presented for thirty-seven shales,four concretions,two carbonate sediments and seven lignites from the Marathousa coal field of the Megalopolis Basin in Greece.The argillaceous rocks consist of chlorite,illite,kaolinte,albite,quartz.opal-A,calcite and dolomite;the concretions of aragonite,gypsum and pyrite;and the carbonate rocks of calcite,quartz and illite.The mineral matter in the lignites consists of gypsum,quartz,albite,chlorite,illite,opal-A,dolomite,pyrite,and rarely calcite and kaolinite Athree-factor model explains the total variaition of major and trace elements in the argillaceous sediments.The first factor is an aluminosilicate factor and involves the following elements:Al,Si,Mg,Na,K,Ti,Mn,Nb,Y,Rb,Zn,Cu,Ni,Cr,Nband V,associated with chlorite,albite and illite.The second factor involves the elements Ca,Sr,Ba,Znand Sc and is related to carbonate lithology and mainly the carbonate concretions with gypsum.The third factor involves Fe and Ce with a weak association with Mn.The diagenesis of the Marathousa sediments and lignites was not very advanced as indicated by (a) the total thickness of the sequence (500m),(b) the presence of biogenic silica(opal-A) and (c) the age of the deposit(Pleistocene).FOr these reasons the rpresence of chlorite,illite and kaolinite in the sediments and lignite is due not to diagenetic reactions but to weathering of the flysch and metamorphic rocks at the edges of the Megalopolis Basin and transport of the weathering products(illite,chlorite,kaolinite)into the basin of deposition.The diagenetic minerals of the Marathousa sequence include pyrite,gypsum,dolomite and aragonite.

  20. Phosphate and feldspar mineralogy of equilibrated L chondrites: The record of metasomatism during metamorphism in ordinary chondrite parent bodies (United States)

    Lewis, Jonathan A.; Jones, Rhian H.


    In ordinary chondrites (OCs), phosphates and feldspar are secondary minerals known to be the products of parent-body metamorphism. Both minerals provide evidence that metasomatic fluids played a role during metamorphism. We studied the petrology and chemistry of phosphates and feldspar in petrologic type 4-6 L chondrites, to examine the role of metasomatic fluids, and to compare metamorphic conditions across all three OC groups. Apatite in L chondrites is Cl-rich, similar to H chondrites, whereas apatite in LL chondrites has lower Cl/F ratios. Merrillite has similar compositions among the three chondrite groups. Feldspar in L chondrites shows a similar equilibration trend to LL chondrites, from a wide range of plagioclase compositions in petrologic type 4 to a homogeneous albitic composition in type 6. This contrasts with H chondrites which have homogeneous albitic plagioclase in petrologic types 4-6. Alkali- and halogen-rich and likely hydrous metasomatic fluids acted during prograde metamorphism on OC parent bodies, resulting in albitization reactions and development of phosphate minerals. Fluid compositions transitioned to a more anhydrous, Cl-rich composition after the asteroid began to cool. Differences in secondary minerals between H and L, LL chondrites can be explained by differences in fluid abundance, duration, or timing of fluid release. Phosphate minerals in the regolith breccia, Kendleton, show lithology-dependent apatite compositions. Bulk Cl/F ratios for OCs inferred from apatite compositions are higher than measured bulk chondrite values, suggesting that bulk F abundances are overestimated and that bulk Cl/F ratios in OCs are similar to CI.

  1. Clay mineralogy of the Boda Claystone Formation (Mecsek Mts., SW Hungary) (United States)

    Németh, Tibor; Máthé, Zoltán; Pekker, Péter; Dódony, István; Kovács-Kis, Viktória; Sipos, Péter; Cora, Ildikó; Kovács, Ivett


    Boda Claystone Formation (BCF) is the host rock of the planned site for high level nuclear waste repository inHungary. Samples representing the dominant rock types of BCF were studied: albitic claystone, claystone with high illite content, and analcime bearing claystone. Clay minerals in these three rock types were characterized by Xray powder diffraction (XRD), transmission electron microscopy (TEM) and thermal analysis (DTA-TG), and the results were discussed from the point of view of the radionuclide sorption properties being studied in the future. Mineral compositions of bulk BCF samples vary in wide ranges. In the albitic sample, besides the dominant illite, few percent of chlorite represents the layer silicates in the clay fraction. Illite is the dominating phase in the illitic sample, with a few percent of chlorite. HRTEM study revealed that the thickness of illite particles rarely reaches 10 layers, usually are of 5-6 TOT layer thick. Illite crystals are generally thicker in the albitic sample than in the illitic one. The significant difference between the clay mineral characterisitics of the analcimous and the other two samples is that the former contains regularly interstratified chlorite/smectite beside the dominant illite. Based on the structural and chemical data two illite type minerals are present in the BCF samples: 1M polytype containing octahedral Fe and Mg besides Al, 2M polytype illite generally is free of Fe andMg. Close association of very thin illite plates and nanosized hematite crystals is typical textural feature for BCF. The goal of this study is to provide solid mineralogical basis for further studies focusing on radionuclide sorption properties.

  2. Geochemistry of Hydrothermal Alteration Associated with Cenozoic Intrusion-Hosted Cu-Pb-Zn Mineralization at Tavşanlı Area, Kütahya, NW Turkey

    Directory of Open Access Journals (Sweden)

    Mustafa Kumral


    Full Text Available The Miocene magmatic intrusion in the Tavşanlı zone of the Kütahya-Bolkardağ Belt (KBB in the northwestern region of Turkey is represented by the Eğrigöz granitoids. This paper studies the petrology and geochemistry of hydrothermal alterations associated with the vein-type Cu-Pb-Zn mineralization hosted by this pluton, focusing on the determination of the mass gains and losses of chemical components, which reflect the chemical exchanges between the host rocks and hydrothermal fluids. Vein-type Cu-Pb-Zn mineralization is closely associated with intense hydrothermal alterations within the brecciation, quartz stockwork veining, and brittle fracture zones that are controlled by NW-SE trending faults cutting through the Eğrigöz granitoids. Paragenetic relationships reveal three stages of mineralization: pre-ore, ore, and supergene. The ore mineralogy typically includes hypogene chalcopyrite, sphalerite, galena, and pyrite, with locally supergene covellite, malachite, and azurite. Wall-rock hypogene hydrothermal alterations include pervasive silicification, sulfidation, sericitization, and selective carbonatization and albitization. These are distributed in three main alteration zones (zone 1: silicified/iron carbonatized alterations ± albite, zone 2: argillic-silicic alterations, and zone 3: phyllic alterations. Based on the gains and losses of mass and volume (calculated by the GEOISO-Windows™ program, zone 1 has a higher mass and volume gain than zones 2 and 3. Non-systematic zonal distributions of alterations are observed in which the silicic-carbonate alterations +/− albitization appeared in zone 1 in the center and the phyllic-argillic alterations appeared in zones 2 and 3, with an increase in base metals (Cu-Pb-Zn in the zone from Cu, Cu-Pb, to Cu-Pb-Zn moving outwards.

  3. U-Pb geochronology of the Lagoa Real uranium district, Brazil: Implications for the age of the uranium mineralization (United States)

    Lobato, Lydia Maria; Pimentel, Márcio Martins; Cruz, Simone C. P.; Machado, Nuno; Noce, Carlos Maurício; Alkmim, Fernando Flecha


    The Lagoa Real uranium district in Bahia, northeastern Brazil, is the most important uranium province in the country and presently produces this metal in an open-pit mine operated by Indústrias Nucleares do Brasil. Uranium-rich zones are associated with plagioclase (dominantly albite ± oligoclase) -rich rocks, albitites and metasomatized granitic-gneisses, distributed along NNW/SSE striking shear zones. We have used the ID-TIMS U-Pb method to date zircon and titanite grains from the São Timóteo granitoid, and albite-rich rocks from the Lagoa Real district in order to assess the age of granite emplacement, deformation/metamorphism and uranium mineralization. The isotopic data support the following sequence of events (i) 1746 ± 5 Ma - emplacement of the São Timóteo granitoid (U-Pb zircon age) in an extensional setting, coeval with the beginning of the sedimentation of the Espinhaço Supergroup; (ii) 956 ± 59 Ma hydrothermal alteration of the São Timóteo granitoid and emplacement of the uranium mineralization (U-Pb titanite age on an albite-rich sample); (iii) 480 Ma metamorphism, remobilization and Pb loss (U-Pb titanite age for the gneiss sample), during the nucleation of shear zones related to the collision between the São Francisco-Congo and Amazonia paleoplates. The 956 ± 59-Ma mineralization age is apparently associated with the evolution of the Macaúbas-Santo Onofre rift. This age bracket may bear an important exploration implication, and should be included in the diverse age scenario of uranium deposits worldwide.

  4. The Petrology and Diagenetic History of the Phacoides Sandstone, Temblor Formation at the McKittrick Oil Field, California (United States)

    Kaess, A. B.; Horton, R. A.


    The McKittrick oil field is located near the western edge of the San Joaquin Basin, California. The oil field is currently in production with 480 wells producing from the Tulare, San Joaquin, Reef Ridge, Monterey, Temblor, Tumey, and Kreyenhagen formations. Within the Temblor Formation production is mainly from the Miocene Carneros and the Phacoides sandstones. Eighty-two samples from the Phacoides sandstone (2403 - 3045 m below surface) were obtained from the California Well Sample Repository to characterize and understand the diagenetic history and its influence on its reservoir properties. Petrographic thin sections were analyzed by quantitative optical petrography, energy dispersive X-ray spectrometry, and imaging with back-scatter electron and cathodoluminescence. The Phacoides sandstone consists of fine to very coarse, poorly to well-sorted, arkosic arenites, and wackes with detrital framework grains including sub-angular quartz, K-feldspar (microcline and orthoclase), plagioclase, and lithic fragments. Ba-free, Ba-rich, and perthitic K-feldspars are present. Accessory minerals include glauconite, biotite, muscovite, magnetite, titanomagnetite, sphene, zircon, apatite, corundum, and rutile. Diagenetic alteration includes: (1) compaction, (2) mineral dissolution, (3) albitization of feldspars, alteration of biotite to pyrite and chlorite, replacement of framework grains by calcite, (4) alteration of volcanic rock fragments, (5) cementation by kaolinite, calcite and dolomite, and (6) precipitation of K-feldspar and quartz overgrowths. Early-formed fractures were healed by authigenic quartz, albite, and K-feldspars. Precipitation of carbonates and clays, rearranging of broken grains, and formation of pseudomatrix reduced primary porosity. Secondary porosity is common and formed initially by the dissolution of plagioclase (excluding albite) and volcanic fragments, and later by dissolution of calcite, dolomite, and detrital K-feldspars. Hydrocarbon emplacement was

  5. 花岗岩类长石相成分换算及其应用

    Institute of Scientific and Technical Information of China (English)



    Based on the data on plagioclase number of granitoids and whole.rock chemical analysis the author has proposed that the percentage of molecules of albite in the coexisting plagioclase and alkali-feldspar can be converted directly by petro-chemical approach. Then, the result is substituted into the formula of J. A. Whitney and J. C. Stormer, Jr. (1975, 1977) in order to work out the temperature during crystallization of the coexisting feldspars, which may represent the diagenetic temperature of host granitoids. Diagenetic temperature values computed by this method as described in the present paper are more accurate than thoes obtained by other geothermometries.

  6. Sorption behavior of U(VI) on phyllite: experiments and modeling (United States)

    Arnold, Thuro; Zorn, T.; Zänker, H.; Bernhard, G.; Nitsche, H.


    The sorption of U(VI) onto low-grade metamorphic rock phyllite was modeled with the diffuse double layer model (DDLM) using the primary mineralogical constituents of phyllite, i.e. quartz, chlorite, muscovite, and albite, as input components, and as additional component, the poorly ordered Fe oxide hydroxide mineral, ferrihydrite. Ferrihydrite forms during the batch sorption experiment as a weathering product of chlorite. In this process, Fe(II), leached from the chlorite, oxidizes to Fe(III), hydrolyses and precipitates as ferrihydrite. The formation of ferrihydrite during the batch sorption experiment was identified by Mössbauer spectroscopy, showing a 2.8% increase of Fe(III) in the phyllite powder. The ferrihydrite was present as Fe nanoparticles or agglomerates with diameters ranging from 6 to 25 nm, with indications for even smaller particles. These Fe colloids were detected in centrifugation experiments of a ground phyllite suspension using various centrifugal forces. The basis for the successful interpretation of the experimental sorption data of uranyl(VI) on phyllite were: (1) the determination of surface complex formation constants of uranyl with quartz, chlorite, muscovite, albite, and ferrihydrite in individual batch sorption experiments, (2) the determination of surface acidity constants of quartz, chlorite, muscovite, and albite obtained from separate acid-base titration, (3) the determination of surface site densities of quartz, chlorite, muscovite, and albite evaluated independently of each other with adsorption isotherms, and (4) the quantification of the secondary phase ferrihydrite, which formed during the batch sorption experiments with phyllite. The surface complex formation constants and the protolysis constants were optimized by using the experimentally obtained data sets and the computer code FITEQL. Surface site densities were evaluated from adsorption isotherms at pH 6.5. The uranyl(VI) sorption onto phyllite was accurately modeled with

  7. Mineral composition of sedimentary matter in the Caspian Sea (United States)

    Lukashin, V. N.; Lisitzin, A. P.; Dara, O. M.; Kozina, N. V.; Klyuvitkin, A. A.; Novigatsky, A. N.


    Data on the mineral composition of sedimentary matter and its fluxes in the sediment system of the Caspian Sea are presented. River runoff, aerosols, particulate matter from sediment traps, and the upper layer (0-1 cm) of bottom sediments are considered. The contents of detrital minerals (quartz, albite, and K-feldspar), clay minerals (illite, chlorite, and kaolinite), and carbonates (calcite, Mg-calcite, dolomite, aragonite, and rhodochrosite) are determined. Gypsum was found in bottom sediments but is absent in the other object of the sediment system.

  8. Thermodynamic conditions of framework grain dissolution of clastic rocks and its application in Kela 2 gas field

    Institute of Scientific and Technical Information of China (English)

    LAI; Xingyun; YU; Bingsong; CHEN; Junyuan; CHEN; Xiaolin


    Feldspar and clastic debris are the most important constituent framework grains of sedimentary clastic rocks and their chemical dissolution plays an essential role in the formation and evolution of the secondary pore in the reservoir rocks. On the basis of thermodynamic phase equilibrium, this study investigates the chemical equilibrium relationships between fluid and various plagioclase and K-feldspar in diagenesis of the sediments, particularly, the impact of temperature and fluid compositions (pH, activity of K+, Na+, Ca2+ and so on) on precipitation and dissolution equilibria of feldspars. Feldspar is extremely easily dissolved in the acid pore water with a low salinity when temperature decreases. The dissolution of anorthite end-member of plagioclase is related to the Ca content of the mineral and the fluid, higher Ca either in the mineral or in the fluid, easier dissolution of the feldspar. Moreover, the dissolution of albite end-member of plagioclase is related to Na of both the mineral and fluid, lower Na out of both the mineral and fluid, easier dissolution of the mineral. Similarly, lower-K fluid is more powerful to dissolve K-feldspar than the higher. The anorthite component of plagioclase is most easily dissolved in ground water-rock system, the albite is the secondary, and K-feldspar is the most stable. Selective dissolution of plagioclase occurs in diagenesis because of the plagioclase solid solution that is mainly composed of albite and anorthite end-members, Ca-rich part of which is preferentially dissolved by the pore water, in contrast to the Na-rich parts. Based on investigation of reservoir quality, secondary pore, dissolution structures of feldspar, clay minerals and ground water chemistry of the Kela 2 gas field of Kuqa Depression in the Tarim basin of Western China, we discovered that the secondary pore is very well developed in the highest quality section of the reservoir, and the plagioclase of which was obviously selectively dissolved, in

  9. Diagenesis of Oligocene continental sandstones in salt-walled mini-basins-Sivas Basin, Turkey (United States)

    Pichat, Alexandre; Hoareau, Guilhem; Callot, Jean-Paul; Ringenbach, Jean-Claude


    The recent discovery of Oligo-Miocene salt-walled continental mini-basins in the Sivas Basin (central Anatolia, Turkey) provides the opportunity to unravel the influence of halokinesis on the diagenesis of continental mini-basin infilling. In this study, petrographic and geochemical analyses are used to define the diagenetic sequences recorded by two mini-basins filled mainly by fluvial clastic sediments of the upper Oligocene Karayün Formation. The initial diagenetic features are those commonly encountered in arid to semi-arid continental environments, i.e. clay infiltration, hematite precipitation and vadose calcite cement. Other early cements were strongly controlled by sandstone detrital composition in the presence of saline/alkaline pore water. In feldspathic litharenites and lithic arkoses, near-surface alterations were characterized by the precipitation of analcime (up to 10%), albite and quartz overgrowths (burial diagenesis which prevented further mesogenetic alteration phenomena such as compaction. In feldsarenites, early diagenesis differs by (i) the absence of analcime, (ii) better developed albite cements, (iii) thin smectite-illite coatings forming pore linings and (iv) patchy calcite cementation (burial, and result in a significant degradation of porosity.

  10. Partial melting of deeply subducted continental crust and the formation of quartzofeldspathic polyphase inclusions in the Sulu UHP eclogites

    Institute of Scientific and Technical Information of China (English)

    ZENG LingSen; LIANG FengHua; ASIMOW Paul; CHEN FangYuan; CHEN Jing


    Two types of quartzofeldspathic inclusions hosted by omphacite and garnet were identified in the Sulu UHP eclogites.The first consists of albite,quartz,and various amounts of K-feldspar.In contrast,the second consists predominantly of K-feldspar and quartz without any albite.The presence of quartzofeldspathic inclusions within the UHP mafic eclogites indicates that partial melting occurred in deeply subducted continental crust via mica dehydration melting reactions at an early stage of rapid exhumation.Such a melting event generated hydrous Na-K-Al-Si melts.These melts infiltrated into the mafic eclogite and were captured by recrystallizing garnet or omphacite,which together followed by dehydration and crystallization to form feldspar-bearing polyphase inclusions.Formation of silicate melts within the deeply subducted continental slab not only provides an excellent medium to transport both mobile (LILE) and immobile (HFSE) elements over a large distance,but also induces effective changes in the physical properties of the UHP slab.This process could be a major factor that enhances rapid exhumation of a deeply subducted continental slab.


    Directory of Open Access Journals (Sweden)

    Akintola O. F


    Full Text Available Pegmatites in Nasarawa area of Central Nigeria lie within a fracture-controlled east-north-east trending rare metal pegmatite belt closely associatedwith late PanAfrican peraluminous granites inNigeria. Trace elements of feldspars andmuscovites of pegmatites inNasarawa area of CentralNigeriawere analyzed to determine the raremetalsmineralization potentials of the pegmatites. The minerals show fractionation even within units of complex mineralizedpegmatites as indicated by the wide ranges of K/Rb in Na-feldspars (albites, muscovites and K-feldspars and the wide range of K/Tl in the latter two minerals. Cs, Rb and Tl and the rare earth elements (REEs Ce, La, Pr and Y are enriched in the K-bearing muscovites and K-feldspars; K-feldspars have the highest average values of Tl, Ce, La, Pr and Y while the muscovites have the highest average values of Sn, Nb, Ga, F and Zn. Average values of Ta, Sr, Ba,Wand Zr are highest in the albites,which also have the lowest averageNb/Ta ratio. This is an indication that these elementsare enriched along lateNa-rich raremetalmineralizing fluids. The rare alkalisRb and Cs and Tl are positively correlated with the rare lithophile elements (Ta, REEs, Pb, Bi and Y, in both the pegmatite K-feldspars and muscovites, strongly positively correlated with Sn in the muscovites but negatively correlated with Nb in the minerals. Inthe pegmatitic albites, Nb has very strong positive correlations with Ta (0.868 and Zr (0.847, which is indicative of the incorporations/substitution of these elements in the crystal lattice of the ore minerals. There is a general enrichment of the rare elements towards themiddle and inner zones of the complexmineralized pegmatites. Fluorine, phosphorus and boron-rich fluids played significant roles in the magmatic complexation/fractionation and concentration of Sn-Ta-Li-Cs-Be in the albitized zones of the highly evolved pagmatites.K/Rb versusCs in theK-feldspars classify the pegmatites into

  12. Rare metal-bearing pegmatites from the Southeastern Desert of Egypt: Geology, geochemical characteristics, and petrogenesis

    Institute of Scientific and Technical Information of China (English)


    The pegmatite province of the Southeastern Desert (SED) is part of a pegmatite district that extends from Egypt (extends to 1200 km2). Rare metal pegmatites are divided into (1) unzoned, Sn-mineralized; (2) zoned Li, Nb, Ta and Be-bearing; and (3) pegmatites and pegmatites containing colored, gem-quality tourmaline. The Rb/Sr data reflect a crustal origin for the rare metal pegmatites and indicate that the original SED magma was generated during the peak of regional metamorphism and predates the intrusion of post-tectonic leucogranites. These bodies developed an early border zone consisting of coarse to very coarse muscovite+quartz+alkali feldspar, followed by an intermediate zone of dominant quartz+feldspar+muscovite rock. Garnet, tourmaline, beryl, galena, pyrite, amblygonite, apatite and monazite are rare accessories in both zones. Cassiterite tends to concentrate in replacement zones and along fractures in albite+quartz+muscovite-rich portions. The highest concentrations of cassiterite occur in irregular greisenized zones which consist dominantly of micaceous aggregates of green Li-rich muscovite, quartz, albite and coarse-grained cassiterite. The different metasomatic post-solidification alterations include sodic and potassic metasomatism, greisenization and tourmalinization. Geochemically, the pegmatite-generating granites have a metaluminous composition, showing a differentiation trend from coarse-grained, unfractionated plagioclase-rich granite towards highly fractionated fine- to medium-grained, local albite-rich rock. Economically important ore minerals introduced by volatile-rich, rare metal-bearing fluids, either primarily or during the breakdown of the primary mineral assemblages, are niobium-tantalum oxides, Sn-oxides (cassiterite), Li-silicates (petalite, spodumene, euctyptite, and pollucite), Li-phosphates (amblygonite, montebrasite and lithopilite) and minor REE-minerals (Hf-zircon, monazite, xenotime, thorian, loparite and yttrio-fluorite). The

  13. Fluid-induced Blueschist Preservation on Syros, Cyclades, Southern Greece (United States)

    Kleine, B. I.; Huet, B.; Skelton, A. D. L.


    Local examples of preservation of high-pressure, low-temperature (HP-LT) mineral assemblages within retrograde metamorphosed greenschist are recorded from the Cyclades, Greece. Several models have been proposed to explain the preservation of HP-LT rocks in these areas. On Sifnos, a capping effect of impermeable marble units below the preserved blueschists caused diversion of the upward, cross-layer infiltration of retrograde fluids [1]. On Tinos, blueschist preservation occurred due to retrograde fluid flow channelization along lithological contacts with high flux rates [2]. HP-LT minerals were preserved in regions adjacent to these contacts where fluid fluxes were smaller. We propose a different mechanism of blueschist preservation based on observations from a costal section near Fabrika on Syros. At this locality a high strain zone cuts through a retrograde greenschist. Along the fault a dark blue halo occurs within the greenschist. Whole rock analyses along a profile from the fault into the greenschist show that only the areas directly adjacent to the deformation zone show chemical evidence of metasomatism, whereas the areas further away are chemically similar to greenschist. Point counting of 1000 evenly spaced points in thin sections of the profile shows a clear blueschist to greenschist transition with a blueschist mineral assemblage (glaucophane+phengite+calcite) nearer to the metasomatic zone and a typical greenschist mineral assemblage (epidote+chlorite+albite) farther away. We propose the following model to explain preservation of HP-LT mineral assemblage in this locality. During retrograde metamorphism a water-rich fluid infiltrated the blueschist rock from below. This occurred close to the brittle-ductile transition. This fluid caused a reaction front to propagate into the overlying blueschist at which its mineral assemblage glaucophane+phengite+calcite was replaced by the greenschist mineral assemblage epidote+albite+chlorite. Upwards-flowing fluid

  14. LCT pegmatites from the Wodgina pegmatite district, Western Australia (United States)

    Richter, Lisa; Dittrich, Thomas; Seifert, Thomas; Schulz, Bernhard


    The lithium-cesium-tantalum (LCT) pegmatites from the Mt. Tinstone and Mt. Cassiterite open pits are located within the Wodgina pegmatite district, about 130 km south of Port Hedland, Western Australia. The albite-spodumene and albite-type pegmatites of the Wodgina pegmatite district are currently mined for tin, tantalum and niobium. The pegmatites are hosted within the Archean East-Pilbara Granite-Greenstone Terrane linked to the fertile Numbana monzogranite that forms part of the Yule Granitoid Complex. Granitic melt intruded into metasedimentary rocks (~2.8 Ga) and formed a series of pegmatite sheets, dikes and irregular structures. These pegmatites are characterized by a high melt fractionation that led to the formation of pegmatitic minerals, containing high concentrations of rare elements, such as Ta, Nb, Li, Rb and Cs. The pegmatites from the Mt. Tinstone sheet open pit, which were investigated within this study, comprises four internal zones consisting of six mineral assemblages, dominated by quartz, albite and white mica, with K-feldspar and spodumene as major or minor constituents. Distribution patterns of cassiterite and Ta-Nb-Sn-oxide minerals (ixiolite/wodginite, tantalite/columbite and microlite) can be observed within the four different pegmatite zones. The contact zones are enriched in cassiterite, ixiolite and microlite; border zones reveal high concentrations of cassiterite, ixiolite and tantalite; the intermediate units are characterized by a moderate enrichment of the ore minerals; whereby core zones host almost no significant contents of the minerals mentioned above. Distribution of Ta-Nb-Sn-oxides within the zones and Mn/(Mn+Fe) and Ta/(Ta+Nb) ratios are indicators for melt fractionation, and change from the core zones to the outermost contact zones, as well as from north to south. Electron microprobe analyses on white mica show the existence of fractionation trends from more primitive white mica of the core zones (zinnwaldite) to higher

  15. Eclogite-High-Pressure Granulite Belt in Northern Edge of the Archean North China Craton

    Institute of Scientific and Technical Information of China (English)


    The discovery of retrograded eclogites and high-pressure basic granulites in the joining region of Hebei-Shanxi-Inner Mongolia (HSIM) abandon the old thoughts that Archean granulites in the North China craton are of middle or low pressure facies and promote the reconsideration of Early Precambrian cratonization tectonic process, and reveal the geological fact that the scale, rigid behavior and geological structure of Archean cratonic blocks have strong similarities to the present fundamental plate tectonics, which suggest new tectonic mechanism to understand the early continental evolution of the North China craton. (1) The retrograded eclogites and high-pressure granulites constitute a ENE-NE-striking structure-rock zone termed as the Sanggan structural belt. (2) The retrograded eclogites are closely associated with high-pressure granulites. We can call this belt a transitional eclogite-granulite facies metamorphic belt. Petrographically three metamorphic stages, at least, in the retrograded eclogite can be distinguished. ① The main mineral assemblage is composed of garnet+clinopyroxene+quartz+rutile. The mineral inclusions in garnet are fine-grained quartz, rutile and small inclusions of fine-grained second stage mineral aggregate. This aggregate consists of hypersthene+albite, and has the typical texture of small hypersthene core surrounded by albite micro-grained grains. ② The second mineral assemblage is represented by corona of garnet and symplectite of clinopyroxene. The corona of garnet is composed of hypersthene+plagioclase+clinopyroxene+a minor amount of quartz and magnetite. The symplectite of clinopyroxene is composed of hypersthene + albite+clinopyroxene. The secondary mineral assemblage along boundaries between quartz and garnet (or clinopyroxene) is fine-grained aggregate of hypersthene and clinopyroxene. ③ The third retrograded metamorphic minerals are mainly amphiboles replacing pyroxenes and plagioclases replacing garnets. The estimated

  16. Crystallization of microlites during magma ascent: the fluid mechanics of 1980 1986 eruptions at Mount St Helens (United States)

    Geschwind, C.-H.; Rutherford, Malcolm J.


    Eruptions of Mount St Helens (Washington, USA) decreased in intensity and explosivity after the main May 18, 1980 eruption. As the post-May 18 eruptions progressed, albitic plagioclase microlites began to appear in the matrix glass, although the bulk composition of erupted products, the phenocryst compositions and magmatic temperatures remained fairly constant. Equilibrium experiments on a Mount St Helens white pumice show that at 160 MPa water pressure and 900°C, conditions deduced for the 8 km deep magma storage zone, the stable plagioclase is An47. The microlites in the natural samples, which are more albitic, had to grow at lower water pressures during ascent. Isothermal decompression experiments reported here demonstrate that a decrease in water pressure from 160 to 2 MPa over four to eight days is capable of producing the albitic groundmass plagioclase and evolved melt compositions observed in post-May 18 1980 dacites. Because groundmass crystallization occurs over a period of days during and after decreases in pressure, microlite crystallization in the Mount St Helens dacites must have occurred during the ascent of each magma batch from a deep reservoir rather than continuously in a shallow holding chamber. This is consistent with data on the kinetics of amphibole breakdown, which require that a significant portion of magma vented in each eruption ascended from a depth of at least 6.5 km (˜160 MPa water pressure) in a matter of days. The size and shape of the microlite population have not been studied because of the small size of the experimental samples; it is possible that the texture continues to mature long after chemical equilibrium is approached. As the temperature, composition, crystal content and water content of magma in the deep reservoir remained approximately constant from May 1980 to at least March 1982, the spectacular decrease in eruption intensity during this period cannot be attributed to changes in viscosity or density of the magma

  17. Strong climate and tectonic control on plagioclase weathering in granitic terrain (United States)

    Rasmussen, C.; Brantley, S.; Richter, D.D.B.; Blum, A.; Dixon, J.; White, A.F.


    Investigations to understand linkages among climate, erosion and weathering are central to quantifying landscape evolution. We approach these linkages through synthesis of regolith data for granitic terrain compiled with respect to climate, geochemistry, and denudation rates for low sloping upland profiles. Focusing on Na as a proxy for plagioclase weathering, we quantified regolith Na depletion, Na mass loss, and the relative partitioning of denudation to physical and chemical contributions. The depth and magnitude of regolith Na depletion increased continuously with increasing water availability, except for locations with mean annual temperature reaction enthalpy for albite. Water availability is suggested as the dominant factor limiting rate kinetics in the water-limited systems. Together, these data demonstrate marked transitions and nonlinearity in how climate and tectonics correlate to plagioclase chemical weathering and Na mass loss. ?? 2010 Elsevier B.V.

  18. Petroleum, oil field waters, and authigenic mineral assemblages - Are they in metastable equilibrium in hydrocarbon reservoirs? (United States)

    Helgeson, Harold C.; Knox, Annette M.; Owens, Christine E.; Shock, Everett L.


    The hypothesis that although the presence of carboxylic acids and carboxylate anions in oil field waters is commonly attributed to the thermal maturation of kerogen or bacterial degradation of hydrocarbons during water-washing of petroleum in relatively shallow reservoirs, they may have also been produced in deeper reservoirs by the hydrolysis of hydrocarbons in petroleum at the oil-water interface is tested. Calculations were carried out to determine the distribution of species with the minimum Gibbs free energy in overpressured oil field waters in the Texas Gulf Coast assuming metastable equilibrium among calcite, albite, and a representative spectrum of organic and inorganic aqueous species at reservoir temperatures and pressures. The hypothesis that homogeneous equilibrium obtains among carboxylate and carbonate species in oil field waters is confirmed.

  19. Geochemical characterization and comparative study of plagiogranites from the South portuguese and Ossa-Morena Zones (SW Iberian Massif, Spain); Caracterizacion geoquimica y estudio comparativo de plagiogranitos de las Zonas Surportuguesa y Ossa-Morena (SO del Macizo Iberico, Espana)

    Energy Technology Data Exchange (ETDEWEB)

    Bellido, F.; Diez-Montes, A.; Sanchez-Garcia, T.


    Plagiogranites and albitic rocks belonging to contrasted magmatic associations of different ages and geo dynamic environments outcrop in Ossa-Morena (OMZ) and Sur portuguese (SPZ) Zones. OMZ plagiogranites are related with Cambrian-Ordovician rifting and represent a part of the felsic members of a bimodal magmatic suite and show oceanic plagiogranites affinities. SPZ plagiogranites are related with a Carboniferous volcano-plutonic calc-alkaline suite related with Variscan Orogeny. Both plagiogranites show many similar petrological and geochemical characteristics but display some different immobile elements ratios as La/Nb, Th/Nb, Th/La that are unaltered by metamorphism, magmatic differentiation and alteration processes and prove differences in their sources. SPZ plagiogranites show a more compositional homogeneity than OMZ ones. This is interpreted as a proof of cogenetic origin for SPZ plagiogranites and heterogeneous origin for OMZ plagiogranites, derived from the mix of different sources (astenospheric, lithospheric and crustal). (Author) 23 refs.

  20. Dacite – siltstone peperite from Trlično at Rogatec, Eastern Slovenia

    Directory of Open Access Journals (Sweden)

    Polona Kralj


    Full Text Available Dacitic glassy lava flow at Trlično is surrounded by a dacite – siltstone peperite and peperitic breccia that underwent alteration, recognised in two, only a few metres thick zones. In the higher-temperature alteration zone, albite extensively replaces volcanic glass and primary plagioclases. The siltstone components are altered to microcrystalline quartz, iron oxides and interlayered illite/smectite clay minerals. This zone developed upon thermalmetamorphosis related to the transfer of heat from the cooling lava. In the lower temperature alteration zone, analcime occurs as the replacement of volcanic glass and pore- and fissure-filling, while the primary plagioclases and poorly lithified siltstone remained fairly unchanged. This zone developed under hydrothermal conditions related to the heating, circulation and reactions of pore waters in the sediment surrounding the lava flow.

  1. Late sodic metasomatism evidences in bimodal volcanic rocks of the Acampamento Velho Alloformation, Neoproterozoic III, southern Brazil

    Directory of Open Access Journals (Sweden)

    Delia Del Pilar M. de Almeida


    Full Text Available A mineralogical study was carried out in mafic and felsic volcanic rocks of the Acampamento Velho Alloformation at Cerro do Bugio, Perau and Serra de Santa Bárbara areas (Camaquã Basin in southern Brazil. The Acampamento Velho bimodal event consists of two associations: lower mafic at the base and upper felsic at the top. Plagioclase and alkali-feldspar were studied using an electronic microprobe, and magnetite, ilmenite, rutile, illite and alkali-feldspar were investigated through scanning electron microscopy. The rocks were affected by a process of late sodic autometasomatism. In mafic rocks, Ca-plagioclase was transformed to albite and pyroxenes were altered. In felsic rocks, sanidine was partially pseudomorphosed, generating heterogeneous alkali-feldspar. In this association, unstable Ti-rich magnetite was replaced by rutile and ilmenite. In mafic rocks, the crystallization sequence was: (1 Ti-rich magnetite (?, (2 pyroxene and Ca-plagioclase, (3 albite (alteration to Ca-plagioclase, (4 sericite, chlorite and calcite (alteration to pyroxene, and kaolinite (alteration to plagioclase/albite. In felsic rocks: (1 zircon, (2 Ti-rich magnetite, (3 sanidine, (4 quartz. The introduction of late Na-rich fluids, generated the formation of (5 heterogeneous alkali-feldspar, (6 ilmenite and rutile from the Ti-rich magnetite, (7 albite in the spherulites. Finally, alteration of sanidine, vitroclasts and pumice to (8 illite.Um estudo mineralógico de detalhe foi realizado nas rochas vulcânicas da Aloformação Acampamento Velho nos Cerros do Bugio, Perau e Serra de Santa Bárbara (Bacia do Camaquã, sudeste do Brasil. Este evento bimodal é constituído por duas associações: máfica inferior na base e félsica superior no topo. Foram estudados grãos de plagioclásio e feldspato alcalino com o uso de microssonda eletrônica, sendo que, magnetita,ilmenita, rutilo e ilita além de feldspato alcalino foram pesquisados através do microscópio eletr

  2. Physicochemical study of ceramics from Pre classic of Cuicuilco 'C' Mexico, methodology to define origin of raw material; Estudio fisico-quimico de ceramica del Preclasico de Cuicuilco 'C' Mexico. Metodologia para definir procedencia de materia prima

    Energy Technology Data Exchange (ETDEWEB)

    Badillo S, A.; Sanchez P, S. [Escuela Nacional de Antropologia e Historia INAH, Periferico Sur y Zapote s/n, Col. Isidro Fabela, Delegacion Tlalpan, Mexico D.F. (Mexico); Perez C, M.A. [Proyecto Arqueologico de Cuicuilco, DEA-INAH, Lic. Verdad 3, Col. Centro (Mexico); Jimenez D, G. [Instituto de Investigaciones Antropologicas de la UNAM, Ciudad Universitaria, 04510 Mexico D.F. (Mexico); Aguilar F, M.; Zorrilla C, C.; Arenas A, J.A. [IFUNAM, Circuito de la Investigacion Cientifica s/n, Ciudad Universitaria, 04510, Mexico D.F. (Mexico)]. e-mail:


    Cuicuilco has been considered one of the most important centers during the Formative Period (1000 - 0 b. C.) in the south of Mexico Basin, mainly, due its dimensions. Because of the Xitle volcano eruption, its occupation decreases around 200 b. C. This paper presents the results of a multidisciplinary investigation about ceramic material from Cuicuilco 'C', located in the south of Mexico City, and sediments from different places near to it. The analysis was done by Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDS) and X- Ray Diffraction (XRD). Its results show the presence of Si, O, Fe and Al as majority elements, and crystalline phases as albite, hematite, quartz, maghemite and cristobalite. Chemical elements identified at ceramic samples has been submitted to an statistical analysis in order to be compared with the results of analyzed sediments, to determinate the raw material origin. (Author)

  3. Mineralogical characterization of quarry fines from Tracuateua city, state of Para, Brazil; Caracterizacao mineralogica dos finos de pedreira do municipio de Tracuateua-PA

    Energy Technology Data Exchange (ETDEWEB)

    Costa, J.H.B. da; Negrao, R.C.; Angelica, R.S., E-mail: [Instituto Federal de Educacao, Ciencia e Tecnologia do Para (IFPA), Belem, PA (Brazil). Departamento de Recursos Naturais. Coordenacao de Mineracao; Universidade Federal do Para (UFPA), Belem, PA (Brazil). Instituto de Geociencias


    The aim of this study was to characterize the mineralogy quarry fines samples for its reuse and thus contributing to mitigate the environmental impact caused by this waste. In order to achieve the results, samples were collected and prepared for assays and identification of the mineralogical phases present in the quarry fines from the samples. X-ray diffraction and optical microscopy techniques were used. The quarry of fines characterization was based on qualitatively identification the minerals present in the samples. It was detected the presence of quartz, muscovite and feldspar (albite and microclinite) by x-ray diffraction technique and microscopic and macroscopic observations. Moreover, the size distribution was determined, and the samples presented a medium to fine size (ranging from 9,5 mm to 0,075 mm) and the grains presented an irregular and angular shapes. (author)

  4. Petrography, mineral chemistry and lithochemistry of the albitite and granite-gneissics rocks of anomaly 35 from Lagoa Real uranium province; Petrografia, quimica mineral e litoquimica do albitito e das rochas granito-gnaissicas da anomalia 35, provincia uranifera de Lagoa Real

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Camila Marques dos


    albitites and gneisses are macroscopically gradational, however, in the garnet albitites replacement of granitic mineral facies by the albitite facies were observed petrographically, implying a granitic protolith for this rock. On the other hand, magnetite albitites do not have clear relationship with granites. Albitites usually have porphyroblastic texture with granoblastic polygonal matrix and chessboard texture in albite porphyroclasts. The garnet albitites comprise hedenbergite, hastingsite, garnet, magnetite and sphena. Magnetite albitites, in turn, have hedenbergite, Fe-edenite, biotite, martitized magnetite, allanite and sphene. The diopside+actinolite+eastonita association is late, and in these rocks, it is restricted to more deformed portions or filling voids. The biotite albitites comprise biotite, zircon and apatite hedenbergite (?). Mineralization occurs in magnetite albitites as thin lenses composed by sphene, magnetite, carbonate and zircon. The uranium mineral is the uraninite, which occurs filling spaces between crystals and sphene or albite granules. In comparison to granites, albitites have a higher content of Na{sub 2}O, MgO, V, W, Zr, Pb and Sr for and lower K{sub 2}O, SiO{sub 2} and F. They have a geochemical REE pattern that is identical to that of granite. The similarity between macroscopic granites and albitites, the presence of vazios, feldspar hematitization and sericitization causing macroscopical reddening in transitional portions and the replacement of potassic feldspar by albite and oligoclase are suggestive of episyenitization processes. The metasomatic perthites and presence of chessboard texture in porphyroclasts indicate successive albitization processes prior to deformation. The comparison between albitite samples of different drill cores and anomalies shows that there are differences in the formation and mineralization of these rocks. The V and Mg enrichment in some albitites suggests that these rocks may result from the interaction of

  5. Zeolitización de rocas andesíticas

    Directory of Open Access Journals (Sweden)

    Plana, F.


    Full Text Available The study of some andesites from King George Island (South Shetland Islands, Anctartica has pointed out the existence of a hydrothermal alteration process going rise to a zeolitic secondary minerals of low-temperature assemblages. Two paragenesis have been identified (Smectite-Bytownite-Mordenite, Smectite-Albite-Laumontite which reflecting different conditions durign the hydrothermal alteration of these andesitic rocksEl estudio de rocas andesíticas de la Isla King George (Archipiélago de las Shetland del Sur, Antártida pone de manifiesto la existencia de procesos de alteración hidrotermal con la formación de minerales zeolíticos secundarios pertenecientes a asociaciones de baja temperatura. Se han identificado dos paragénesis (Esmectitas-Bytownita-Mordenita, Esmectitas-AlbitaLaumontita que reflejan distintas condiciones durante la alteración hidrotermal de dichas rocas andesíticas.

  6. Mineralogy, geochemistry, porosity and redox properties of rocks from Forsmark. Compilation of data from the regional model volume for SR-Site

    Energy Technology Data Exchange (ETDEWEB)

    Sandstroem, Bjoern (WSP Sverige AB, Stockholm (Sweden)); Stephens, Michael B. (Geological Survey of Sweden, Uppsala (Sweden))


    This report is a compilation of the data acquired during the Forsmark site investigation programme on the mineralogy, geochemistry, redox properties and porosity of different rock types at Forsmark. The aim is to provide a final summary of the available data for use during the SR-Site modelling work. Data presented in this report represent the regional model volume and have previously been published in various SKB reports. The data have been extracted from the SKB database Sicada and are presented as calculated median values, data range and lower/upper quartile. The representativity of all samples used for the calculations have been evaluated and data from samples where there is insufficient control on the rock type have been omitted. Rock samples affected by alteration have been omitted from the unaltered samples and are presented separately based on type of alteration (e.g. oxidised or albitized rock)

  7. Chemical and mineralogical characterization of archaeologicam building materials from Seyitomer Hoyuk Kutahya, Turkey. (United States)

    Bilgen, Nejat; Olgun, Asim

    This paper focuses on the spectroscopic and thermal analysis of the archaeological samples of mortar and plaster from middle Bronze Age and Achaemenid period in Seyitömer Höyük. The composition of the samples was investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy and thermogravimetric thermal analysis (TG-DTA). The results showed that human used different types of raw materials in the preperation of the mortar and plaster in the Middle Bronze Age and Achaemenid period. The material used in middle Bronze Age contains muscovite whereas the material in Achaemenid period contains albite. Although, the chemical composition of the mortar and plaster used in the period were similar, the calcium content of the plaster is relatively higher than the one of the mortar indicating people's awareness of the binding properties of calcite.

  8. 碱交代与铁矿形成的地球化学机理探讨

    Institute of Scientific and Technical Information of China (English)



    Discussions are given to the processes of albitization and iron activation during the formation of iron deposits, the transportation and hydrolysis of iron, chemical reactions characteristic of wall rock alteration responsible for the localization of iron deposits, the dynamic factors affecting these reactions as well as the systematic pH variation of ore forming solutions. A metasomatic series of Na→Ca→Fe is noticed when diorite and dark minerals + anorthite + quartz are reacted with 1--3N NaCl solution at 400-500℃。Hydrolysis of FeCl3 is experimentally studied as a function of temperature and pressure.The authors suggest that the pH of ore forming solution varies in the direction of alkalic→ intermediate→acid→intermediate→alkalic from eariler to later stages.

  9. Some geochemical characteristics of alkaline rocks of the Mada Younger Granite complex, Nigeria (United States)

    Abaa, S. I.

    Some geochemical aspects of the Mada Younger Granite complex are considered. The granites are petrologically classified as A-type, of long time duration, with chemical differences arising from the variation in the A/CNK ratio. The CPW norms show a decrease in anorthite and an increase in corundum in the granites associated with disseminated and vein type cassiterite mineralization. The KRb diagram shows that rocks of the Mada massif crystallized within a pegmatitic-hydrothermal trend. Some chondrite-normalized transition elements indicate that the rocks unaffected by fluid reaction were derived by fractional crystallization. The enhancement of some LIL elements, heavy rare-earths and a decrease in the magnitude of Eu depletion, particularly in the albitized variants of the granites, point to postmagmatic rock-fluid metasomatism and accompanying mineralization.

  10. Pervasive, high temperature hydrothermal alteration in the RN-17B drill core, Reykjanes Geothermal System-Iceland Deep Drilling Project (United States)

    Zierenberg, R. A.; Schiffman, P.; Marks, N. E.; Reed, M. H.; Elders, W. A.; Fridleifsson, G. O.


    In November 2008, 9.5 m of core were recovered from Reykjanes production well RN-17B at a depth of 2800m. The core consists mainly of hyaloclastite breccias, hetrolithic breccias with clasts of crystalline basalt, and volcaniclastic sandstones/siltstones. Much of the material appears to have been transported and redeposited, but homolithic breccias and hyaloclastites, some with upright flow lobes of basalt with quenched rims, are interpreted to have erupted in situ. Fine-scale features (glass rims, quench crystals, vesicles, phenocrysts) are well preserved, but all lithologies are pervasively hydrothermally altered such that primary clinopyroxene is ubiquitously uralitized and primary plagioclase (An42-80) is replaced by albite and/or more calcic plagioclase. In contrast, cuttings of similar lithologies, recovered by rotary drilling in intervals immediately above and below the core, exhibit much lesser degrees of hydrothermal alteration and commonly contain igneous plagioclase and clinopyroxene. Vitric clasts in the core are recrystallized into aggregates of chlorite and actinolite. In some breccias, cm-scale metadomains are composed of patchy albite or actinolite/magnesiohornblende giving the core a green and white spotted appearance. Minor amounts (<1%) of disseminated pyrite occur throughout the core, but two intervals with more abundant sulfide contain chalcopyrite and sphalerite in addition to pyrite. Amygdales and vugs in the breccias, initially filled with chlorite, actinolite, epidote, and/or albite, have been partly overprinted with hornblende and anorthite. The core is cut in places by < 1 cm- wide veins composed of early epidote + actinolite + titanite and later anorthite + magnesiohornblende/pargasite. Quartz is not present in any alteration domains observed in the core, although it is reported from virtually all of the cutting intervals above and below the cored section. Seawater-basalt reaction calculations suggest that albite formed during early

  11. Thermoluminescence properties of Chile Guajillo (paprika) Mexicano

    Energy Technology Data Exchange (ETDEWEB)

    Kitis, G. [Nuclear Physics Laboratory, Aristotle University of Thessaloniki, Thessaloniki 54124 (Greece)]. E-mail:; Cruz Zaragoza, E. [Institute of Nuclear Science, UNAM, PO Box 70-753, Mexico DF (Mexico); Furetta, C. [Physics Department, University La Sapienza, P.le A. Moro 2. 00187 Rome (Italy)


    The thermoluminescence properties of the inorganic dust extracted from the Chile Guajillo (paprika) Mexicano, were studied in order to verify the possibility of using the TL technique to discriminate between irradiated and non irradiated peppers. The inorganic dust was found to consist of quartz 60%, albite (NaAlSi{sub 3}O{sub 8}) 30%, and ortose (KAlSi{sub 3}O{sub 8}) 10%. Its thermoluminescence dose response covers the wide dose range of 1Gy-10kGy, which was attributed mainly to feldspars. Its high sensitivity and its stability over 10 irradiation-readout cycles allow the application of a single grain-single aliquot regeneration dosimetry in Chile Guajillo (paprika). Evaluations based on trapping parameters show that thermal fading at room temperature for glow-peaks above 180 deg.. C, is not a problem in the dosimetry of paprika.


    Directory of Open Access Journals (Sweden)

    Vladimir Majer


    Full Text Available Metharyolites of Vranica mountain are roks of emphasized porphyritic texture containing phenocrysts of quartz, K.feldspar and very rarely albite. The groundmass is microcrystallinic, characterized by finegrained phengite, biotite and area consisting of granophyric intergrowths of quartz and feldspar. Accessory minerals are ilmenite, rutila, apatite, zircon and chlorite. Metarhyolites are peraulminous rocks (PI=1.-4.1 having dominantly potassium character (K2O/Na2O=1,3-13,8. Incompatible elements are enriched relative to the normalizing chondrite composition, pointing to the crustal origin of metarhyolite magma. Although phengites typically occur in high pressure rocks, it seems that phengites of metarhyolites of Vranica mountain belong to the seldom group of phengites occurring in the low to medium pressure rocks (the paper is published in Croatian.

  13. 某地钽铌钨铍矿化花岗岩

    Institute of Scientific and Technical Information of China (English)



    The tantalum-, niobium-, tungsten-, beryllium-mineralized granite described in this paper is identified as albitizied fine-grained muscovite granite and occurs as a small discordant taeolity with a bulging central part, dipping and finning out outwards.A crust of quartz-pegmatoid, several tens of centimeters thick, dsvelopes in its apices. Major rock-forming minerals are plagioclase, mierocline, albite, muscovite and quartz. Partsehinite, fluorite and topaz are characteristically abundant among accessory minerals. Rare element and base metal minerals include wolframite,scbeellte, microlite, raanganese-rich columbite, berly, phenacite, xenotirae, monazite,cassitcrite, raolybdenite, bisrauthinite, etc. Niobium and beryllium mineralizations are uniformly present throughout the rock body, but tantalum is feund richer in upper parts than in lower parts. It is tentatively suggested that this is a differentiationmctasomatic deposit of fracture-filling type originated during late magmatic stage.

  14. Petrology of Impact-Melt Rocks at the Chicxulub Multiring Basin, Yucatan, Mexico (United States)

    Schuraytz, Benjamin C.; Sharpton, Virgil L.; Marin, Luis E.


    Compositions and textures of melt rocks from the upper part of the Chicxulub structure are typical of melt rocks at other large terrestrial impact structures. Apart from variably elevated iridium concentrations (less than 1.5 to 13.5 +/- 0.9 ppb) indicating nonuniform dissemination of a meteoritic component, bulk rock and phenocryst compositions imply that these melt rocks were derived exclusively from continental crust and platform-sediment target lithologies. Modest differences in bulk chemistry among samples from wells located approximately 40 km apart suggest minor variations in relative contributions of these target lithologies to the melts. Subtle variations in the compositions of early-formed pyroxene and plagioclase also support minor primary differences in chemistry between the melts. Evidence for pervasive hydrothermal alteration of the porous mesostasis includes albite, K-feldspar, quartz, epidote, chlorite, and other phyllosilicates, as well as siderophile element-enriched sulfides, suggesting the possibility that Chicxulub, like Sudbury, may host important ore deposits.

  15. Alkali based slagging: a case study from Leigh Creek

    Energy Technology Data Exchange (ETDEWEB)

    R.A. Creelman; J. Bamberry; L.A. Juniper; C. Ward [University of Western Sydney, Penrith South, NSW (Australia)


    A systematic study was undertaken at NRG Port Augusta Power station in South Australia to determine the cause of ash deposition (slagging) in the boilers. Conventional wisdom suggests that iron in the ash is generally a major player in furnace ash deposition; however, mineralogical and chemical analyses of the deposits showed that the binding phase was plagioclase feldspar, dominated by the sodic feldspar albite. The study resulted in recognition that the cause of the formation of ash deposits in the North Flinders furnaces was the result of the ingestion of sodium and calcium into the melt that bound the deposits. This finding was a breakthrough in understanding the deposition process within these furnaces, and emphasises that not all slagging is iron related and that systematic studies of deposits, coal and ash make fundamental contributions to understanding the ash deposition mechanisms. 9 refs., 5 figs., 2 tabs.

  16. Morro do Rocio - an unequilibrated H5 chondrite (United States)

    Fredriksson, K.; Wlotzka, F.


    The results of an intensive study of apparently anomalous features of the Morro do Rocio (MDR) chondrite are reported. The examination was undertaken because of the detection of what appeared to be tridymite spherules. Chemical, petrological and mineralogical analyses were performed. The analyses indicated that the features thought to anomalous were in reality artifacts taken out of context. Some olivines and pyroxenes with Fe/Mg ratios which deviated from an equilibrated structure were observed, along with free SiO2 close to the olivine. K-feldspar was found to have separated from the albitic-diopsidic residual glass (or melt). The scale of the observed anomalies was finer than the scale usually used in examining chondrites, implying that chondrites will normally display some anomalies if examined on a fine enough scale.

  17. Effects of fluid-assisted diffusion on texture strength in a mylonitised metagabbro (United States)

    Gardner, Joseph; Wheeler, John; Mariani, Elisabetta


    Most rocks are polyphase materials yet many studies of rock texture tend to isolate the behaviour of individual phases. Characterisation of interaction between phases can yield useful information about the deformation behaviour of real rocks. Our work focuses on a broadly two phase mixture of albite and clinozoisite in mylonitised metagabbros, and how these two phases may have interacted to create, maintain and/or weaken the variable strength CPOs observed in each phase. Intriguingly, the rocks have deformed primarily by diffusion-accommodated processes, which are traditionally thought to weaken or destroy an existing CPO. Our data suggest that diffusion can preserve strong textures. Plagioclase in metamorphosed gabbros from a km-scale extensional shear zone in the NW Italian Alps (Gressoney Shear Zone) has undergone (to a first order) breakdown to albite (Ab) + clinozoiste (Cz) at greenschist facies. Grain size reduction via nucleation of product grains, plus the effects of Zener pinning, lead to an average grain size of 100 μm, which suggests grain growth elsewhere in the matrix was indeed inhibited by the presence of a second phase. Discrete CPO bands vary in size. Variations in grain and grain boundary characteristics between domains are being quantified to investigate whether the way an inherited orientation relates to L-S sample geometry may have had any control over degree of dissolution (implied from grain morphology) within domains. Whether volume fraction of Cz in (what remains of) each domain has influenced dissolution will also be characterised by quantifying grain shape, orientation and distribution of phases in individual domains.

  18. Geochemical modeling of diagenetic reactions in Snorre Field reservoir sandstones: a comparative study of computer codes

    Directory of Open Access Journals (Sweden)

    Marcos Antonio Klunk

    Full Text Available ABSTRACTDiagenetic reactions, characterized by the dissolution and precipitation of minerals at low temperatures, control the quality of sedimentary rocks as hydrocarbon reservoirs. Geochemical modeling, a tool used to understand diagenetic processes, is performed through computer codes based on thermodynamic and kinetic parameters. In a comparative study, we reproduced the diagenetic reactions observed in Snorre Field reservoir sandstones, Norwegian North Sea. These reactions had been previously modeled in the literature using DISSOL-THERMAL code. In this study, we modeled the diagenetic reactions in the reservoirs using Geochemist's Workbench (GWB and TOUGHREACT software, based on a convective-diffusive-reactive model and on the thermodynamic and kinetic parameters compiled for each reaction. TOUGHREACT and DISSOL-THERMAL modeling showed dissolution of quartz, K-feldspar and plagioclase in a similar temperature range from 25 to 80°C. In contrast, GWB modeling showed dissolution of albite, plagioclase and illite, as well as precipitation of quartz, K-feldspar and kaolinite in the same temperature range. The modeling generated by the different software for temperatures of 100, 120 and 140°C showed similarly the dissolution of quartz, K-feldspar, plagioclase and kaolinite, but differed in the precipitation of albite and illite. At temperatures of 150 and 160°C, GWB and TOUGHREACT produced different results from the DISSOL-THERMAL, except for the dissolution of quartz, plagioclase and kaolinite. The comparative study allows choosing the numerical modeling software whose results are closer to the diagenetic reactions observed in the petrographic analysis of the modeled reservoirs.

  19. Thermoluminescence response of the poly mineral fraction from hibiscus sabdariffa L foodstuffs

    Energy Technology Data Exchange (ETDEWEB)

    Cruz Z, E.; Guzman, S. [UNAM, Instituto de Ciencias Nucleares, Apdo. Postal 70-543, 04510 Mexico D. F. (Mexico); Brown, F. [Universidad de Sonora, Departamento de Investigacion en Polimeros y Materiales, Apdo. Postal 130, 83000 Hermosillo, Sonora (Mexico); Chernov, V.; Barboza F, M., E-mail: ecruz@nucleares.unam.m [Universidad de Sonora, Departamento de Investigacion en Fisica, Apdo. Postal 5-088, 83190 Hermosillo, Sonora (Mexico)


    Food processed by ionizing irradiation is a safe technology and has been recognized by the FAO/Who Codes Alimentarius Commission. It is an excellent method to prevent food spoilage and food borne diseases by inhibiting the growth of microorganisms and slowing down ripening. The widespread use of food irradiation treatments that include spices, dry vegetables, grains and fruits make relevant the developing of methods for identification and analyses of foodstuffs processed by irradiation. The present work focuses on the thermoluminescence property of Mexican Roselle flower previously irradiated for detection purposes. The poly mineral content of irradiated commercial Roselle flower (Hibiscus sabdariffa L.) was extracted and analyzed by thermoluminescence (Tl). The X-ray diffraction analyses showed that quartz and albite composition for the poly mineral fraction. Different grain sizes; 10, 53, 74 and 149 {mu}m, were selected for the Tl analyses. The Tl glow curves depended on the grain sizes. The glow curves depicted two peaks around 92 and 120 C. The first peak was ascribed to quartz and the broad part of the glow curves (120-250 C) seems to correspond to the albite. Because the complex structure of the Tl glow curves from poly minerals the kinetic parameters were calculated by a fitting process using a deconvolution method based on a non-linear least-squares Levenberg-Ma quart. The values of the activation energy were found to be at 0.79-1.05 eV and 0.79-1.04 for 53 {mu}m and 250 {mu}m, respectively. The Tl properties of the samples were determined including dose response, reproducibly, fading and UV light bleaching. (Author)

  20. Three-Dimensional Modeling of the Reactive Transport of CO2 and Its Impact on Geomechanical Properties of Reservoir Rocks and Seals

    Energy Technology Data Exchange (ETDEWEB)

    Nguyen, Ba Nghiep; Hou, Zhangshuan; Bacon, Diana H.; Murray, Christopher J.; White, Mark D.


    This article develops a novel multiscale modeling approach to analyze CO2 reservoirs using Pacific Northwest National Laboratory’s STOMP-CO2-R code that is interfaced with the ABAQUS® finite element package. The STOMP-CO2-R/ABAQUS® sequentially coupled simulator accounts for the reactive transport of CO2 causing mineral composition changes that modify the geomechanical properties of reservoir rocks and seals. Formation rocks’ elastic properties that vary during CO2 injection and govern the poroelastic behavior of rocks are modeled by an Eshelby-Mori-Tanka approach (EMTA) implemented in ABAQUS® via user-subroutines. The computational tool incorporates the change in rock permeability due to both geochemistry and geomechanics. A three-dimensional (3D) STOMP-CO2-R model for a model CO2 reservoir containing a vertical fault is built to analyze a formation containing a realistic geochemical reaction network with 5 minerals: albite, anorthite, calcite, kaolinite and quartz. A 3D ABAQUS® model that maps the above STOMP-CO2-R model is built for the analysis using STOMP-CO2-R/ABAQUS®. The results show that the changes in volume fraction of minerals include dissolution of anorthite, precipitation of calcite and kaolinite, with little change in the albite volume fraction. After a long period of CO2 injection the mineralogical and geomechanical changes significantly reduced the permeability and elastic modulus of the reservoir (between the base and caprock) in front of the fault leading to a reduction of the pressure margin to fracture at and beyond the injection location. The impact of reactive transport of CO2 on the geomechanical properties of reservoir rocks and seals are studied in terms of mineral composition changes that directly affect the rock stiffness, stress and strain distributions as well as the pressure margin to fracture.

  1. Alteration and mineralization of an oceanic forearc and the ophiolite-ocean crust analogy (United States)

    Alt, J.C.; Teagle, D.A.H.; Brewer, T.; Shanks, Wayne C.; Halliday, A.


    Mineralogical, chemical, and isotopic (O, C, S, and Sr) analyses were performed on minerals and bulk rocks from a forearc basement section to understand alteration processes and compare with mid-ocean ridges (MOR) and ophiolites. Ocean Drilling Program Hole 786B in the Izu-Bonin forearc penetrates 103 m of sediment and 725 m into volcanic flows, breccias, and basal dikes. The rocks comprise boninites and andesites to rhyolites. Most of the section was affected by low-temperature (Mg, Fe, Sr, and Y, and elevated ??18O and 87Sr/86Sr. Higher temperatures (???150??C) in the basal dikes below 750 m led to more intense alteration and formation of chlorite-smectite, corrensite, albite, K-feldspar, and quartz (??chlorite). A 5 m thick hydrothermally altered and pyritized zone at 815 m in the basal dikes reacted with mixtures of seawater and hydrothermal fluids to Mg-chlorite, albite, and pyrite, and gained Mg and S and lost Si and Ca. Focused flow of hydrothermal fluids produced sericitization halos (Na-K sericite, quartz, pyrophyllite, K-feldspar, and pyrite) along quartz veins at temperatures of 200??-250??C. High 87Sr/86Sr ratios of chloritized (???0.7055) and sericitized (???0.7065) rocks indicate involvement of seawater via mixing with hydrothermal fluids. Low ??34S of sulfide (???2 to -5.5???) and sulfate (12.5???) are consistent with input of magmatic SO2 into hydrothermal fluids and disproportionation to sulfide and sulfate. Alteration processes were generally similar to those at MORs, but the arc section is more intensively altered, in part because of the presence of abundant glassy rocks and mafic phases. The increase in alteration grade below 750 m and the mineralization in the basal dikes are analogous to changes that occur near the base of the volcanic section in MOR and the Troodos ophiolite.

  2. Tourmaline from the Archean G.R.Halli gold deposit, Chitradurga greenstone belt, Dharwar craton (India):Implications for the gold metallogeny

    Institute of Scientific and Technical Information of China (English)

    Susmita Gupta; M. Jayananda; Fareeduddin


    Tourmaline occurs as a minor but important mineral in the alteration zone of the Archean orogenic gold deposit of Guddadarangavanahalli (G.R.Halli) in the Chitradurga greenstone belt of the western Dharwar craton, southern India. It occurs in the distal alteration halo of the G.R.Halli gold deposit as (a) clusters of very fine grained aggregates which form a minor constituent in the matrix of the altered metabasalt (AMB tourmaline) and (b) in quartz-carbonate veins (vein tourmaline). The vein tourmaline, based upon the association of specific carbonate minerals, is further grouped as (i) albite-tourmaline-ankerite-quartz veins (vein-1 tourmaline) and (ii) albite-tourmaline-calcite-quartz veins (vein-2 tourmaline). Both the AMB tourmaline and the vein tourmalines (vein-1 and vein-2) belong to the alkali group and are clas-sified under schorl-dravite series. Tourmalines occurring in the veins are zoned while the AMB tour-malines are unzoned. Mineral chemistry and discrimination diagrams reveal that cores and rims of the vein tourmalines are distinctly different. Core composition of the vein tourmalines is similar to the composition of the AMB tourmaline. The formation of the AMB tourmaline and cores of the vein tour-malines are proposed to be related to the regional D1 deformational event associated with the emplacement of the adjoining ca. 2.61 Ga Chitradurga granite whilst rims of the vein tourmalines vis-à-vis gold mineralization is spatially linked to the juvenile magmatic accretion (2.56e2.50 Ga) east of the studied area in the western part of the eastern Dharwar craton.

  3. The Canastra Group in the type-area, Tapira region, southwest of Minas Gerais State, Brazil

    Directory of Open Access Journals (Sweden)

    Carlos Humberto da Silva


    Full Text Available This work aimed at describing the Neoproterozoic evolution of a Southern Brasília Fold Belt segment, in Tapira area(southwest of Minas Gerais state, Brazil, using detailed geologic mapping. This area, the Canastra Group type-area, hasshowed great tectonic and stratigraphic complexities unlike the simplicity suggested in previous works. From recognizingthe main tectonic discontinuities, it was possible to subdivide the area into some domains. In the west domain, they wereindividualized in tectonic sheet I, marked by pelitic rocks and pelitic-graphite rocks with psammitic intercalations, and II,pelitic rocks with psammitic and mafic-ultramafic intercalations overlapped by gneisses. In the east domain, a group ofthree tectonic sheets was defined, in which, in the two lower tectonic sheets, pelitic and pelitic-graphite rocks with psammiticrock intercalations prevailed, which is different in metamorphic conditions. The lower tectonic sheet is marked bymineralogical associations with muscovite + chlorite + quartz ± graphite ± albite, without biotite; however, the superior oneis with muscovite + quartz + garnet ± chlorite ± biotite ± chloritoid ± graphite ± albite. In the upper tectonic sheet, peliticrocks with local contributions of psammitic and ultramafics rocks occur. In the south domain, psammitic rocks basically occur with contributions of pelitics and rudaceous rocks, where the preservation of textures and sedimentary structures is common.Rocks of the several domains are interpreted as part of a passive continental margin basin, located in the western margin of the SãoFrancisco paleocontinent. Thus, the south domain rocks would represent the facies of proximal platform; rocks of the lower and middle tectonic sheets (east domain and of the tectonic sheet I (west domain are of facies distal platform; and the ones from the upper tectonic sheet (east domain and tectonic sheet II (west domain were acknowledged as deposited in an environment

  4. Mass change calculations of hydrothermal alterations within the volcanogenic metasediments hosted Cu-Pb (-Zn) mineralization at Halilar area, NW Turkey (United States)

    Kiran Yildirim, Demet; Abdelnasser, Amr; Doner, Zeynep; Kumral, Mustafa


    The Halilar Cu-Pb (-Zn) mineralization that is formed in the volcanogenic metasediments of Bagcagiz Formation at Balikesir province, NW Turkey, represents locally vein-type deposit as well as restricted to fault gouge zone directed NE-SW along with the lower boundary of Bagcagiz Formation and Duztarla granitic intrusion in the study area. Furthermore, This granite is traversed by numerous mineralized sheeted vein systems, which locally transgress into the surrounding metasediments. Therefore, this mineralization closely associated with intense hydrothermal alteration within brecciation, and quartz stockwork veining. The ore mineral assemblage includes chalcopyrite, galena, and some sphalerite with covellite and goethite formed during three phases of mineralization (pre-ore, main ore, and supergene) within an abundant gangue of quartz and calcite. The geologic and field relationships, petrographic and mineralogical studies reveal two alteration zones occurred with the Cu-Pb (-Zn) mineralization along the contact between the Bagcagiz Formation and Duztarla granite; pervasive phyllic alteration (quartz, sericite, and pyrite), and selective propylitic alteration (albite, calcite, epidote, sericite and/or chlorite). This work, by using the mass balance calculations, reports the mass/volume changes (gain and loss) of the chemical components of the hydrothermal alteration zones associated with Halilar Cu-Pb (-Zn) mineralization at Balikesir area (Turkey). It revealed that the phyllic alteration has enrichments of Si, Fe, K, Ba, and LOI with depletion of Mg, Ca, and Na reflect sericitization of alkali feldspar and destruction of ferromagnesian minerals. This zone has high Cu and Pb with Zn contents represents the main mineralized zone. On the other hand, the propylitic zone is characterized by addition of Ca, Na, K, Ti, P, and Ba with LOI and Cu (lower content) referring to the replacement of plagioclase and ferromagnesian minerals by albite, calcite, epidote, and sericite

  5. The role of diffusion-controlled oscillatory nucleation in the formation of line rock in pegmatite-aplite dikes (United States)

    Webber, K.L.; Falster, A.U.; Simmons, W.B.; Foord, E.E.


    The George Ashley Block (GAB), located in the Pala Pegmatite District, San Diego County, California, is a composite pegmatite-aplite dike of 8 m thickness displaying striking mineralogical layering in the aphte portion of the dike, referred to as line rock. Rhythmic layering is characterized by garnet-rich bands alternating with albite-quartz-muscovite-rich bands. Cumulus textures are notably absent from the layered portion of the dike. Elongated quartz, megacrysts are oriented perpendicular to the garnet-rich layers and poikilitically include garnet, albite, and muscovite. Calculated crystal-free magma viscosity with 3% H2O is 106.2 Pa s and the calculated settling velocity for garnet is 0??51 cm/year. Conductive cooling calculations based on emplacement of a 650??C dike into 150?? C fractured gabbroic country rock at 1??5 kbar, and accounting for latent heat of crystallization, demonstrate that the line rock portion of the dike cools to 550?? C in about 1 year. Crystal size distribution studies also suggest very rapid nucleation and crystallization. Diffusion-controlled gel crystallization experiments yield textures virtually identical to those observed in the layered aplite, including rhythmic banding, colloform layering, and band discontinuities. Thus, observed textures and calculated magmatic parameters suggest that mineralogical layering in the GAB results from an in situ diffusion-controlled process of oscillatory nucleation and crystallization. We propose that any event that promotes strong undercooling has the potential to initiate rapid heterogeneous nucleation and oscillatory crystal growth, leading to the development of a layer of excluded components in front of the crystallization front, and the formation of line rock.

  6. Contribution of long-term hydrothermal experiments for understanding the smectite-to-chlorite conversion in geological environments (United States)

    Mosser-Ruck, Régine; Pignatelli, Isabella; Bourdelle, Franck; Abdelmoula, Mustapha; Barres, Odile; Guillaume, Damien; Charpentier, Delphine; Rousset, Davy; Cathelineau, Michel; Michau, Nicolas


    The smectite-to-chlorite conversion is investigated through long-duration experiments (up to 9 years) conducted at 300 °C. The starting products were the Wyoming bentonite MX80 (79 % smectite), metallic iron and magnetite in contact with a Na-Ca chloride solution. The predominant minerals in the run products were an iron-rich chlorite (chamosite like) and interstratified clays interpreted to be chlorite/smectite and/or corrensite/smectite, accompanied by euhedral crystals of quartz, albite and zeolite. The formation of pure corrensite was not observed in the long-duration experiments. The conversion of smectite into chlorite over time appears to take place in several steps and through several successive mechanisms: a solid-state transformation, significant dissolution of the smectite and direct precipitation from the solution, which is over-saturated with respect to chlorite, allowing the formation of a chamosite-like mineral. The reaction mechanisms are confirmed by X-ray patterns and data obtained on the experimental solutions (pH, contents of Si, Mg, Na and Ca). Because of the availability of some nutrients in the solution, total dissolution of the starting smectite does not lead to 100 % crystallization of chlorite but to a mixture of two dominant clays: chamosite and interstratified chlorite/smectite and/or corrensite/smectite poor in smectite. The role of Fe/(Fe + Mg) in the experimental medium is highlighted by chemical data obtained on newly formed clay particles alongside previously published data. The newly formed iron-rich chlorite has the same composition as that predicted by the geothermometer for diagenetic to low-grade metamorphic conditions, and the quartz + Fe-chlorite + albite experimental assemblage in the 9-year experiment is close to that fixed by water-rock equilibrium.

  7. Chemical evolution of saline waters in the Jordan-Dead Sea transform and in adjoining areas (United States)

    Möller, Peter; Rosenthal, Eliyahu; Geyer, Stefan; Flexer, Akiva


    The Ca Mg relationship in groundwaters strongly points to the overall dolomitization and local albitization. The Mg/Ca ratios reveal two trends by which saline waters develop: increase of Mg/Ca ratio by evaporation and decreasing Mg/Ca ratios due to dolomitization and albitization. Br/Cl vs. Na/Cl ratios demonstrate that albitization does not play a major role which leaves dolomitization to be the main source for decreasing Mg/Ca ratios in saline waters. In the eastern and southern Region of Lake Kinneret, salinization occurs by mixing with a Ca/Mg molar ratio 1 dominates, which developed by the albitization of plagioclase in abundant mafic volcanics and the dolomitization of limestones. The most saline groundwater of the Tabgha-, Fuliya-, and Tiberias clusters could be regional derivatives of at least two mother brines: in diluted form one is represented by Ha’On water, the other is a Na-rich brine of the Zemah type. Additionally, a deep-seated Ca-dominant brine may ascend along the fractures on the western side of Lake Kinneret, which is absent on the eastern side. Groundwaters of the Lower Jordan Valley are chemically different on both sides of the Jordan River, indicating that the exchange of water is insignificant. All saline waters from the Dead Sea and its surroundings represent a complex mixture of brines, and precipitation and local dissolution of halite and gypsum. Many wells of the Arava/Araba Valley pump groundwater from the Upper Cretaceous limestone aquifer, the origin of the water is actually from the Lower Cretaceous Kurnub Group sandstones. Groundwater drawn from the Quaternary alluvial fill either originates from Kurnub Group sandstones (Eilat 108, Yaalon 117) or from altered limestones of the Judea Group. The origin of these waters is from floods flowing through wadis incised into calcareous formations of the Judea Group. On the other hand, as a result of step-faulting, hydraulic contact is locally established between the Kurnub- and the Judea

  8. Mineral Chemistry and Precipitation Kinetics of Dawsonite in the Geological Sequestration of CO2 (United States)

    Duan, R.; Carey, J. W.; Kaszuba, J. P.


    Dawsonite [NaAl(OH)2CO3] is a relatively rare mineral that may play an important role in the geological sequestration of CO2: thermodynamic and reactive transport calculations predict that dawsonite should precipitate under a variety of CO2 injection scenarios by dissolution of Al-bearing minerals in Na-bearing brine. The precipitation of dawsonite is potentially beneficial as a means of fixing the CO2 in solid form but could also modify porosity and permeability. The relative rarity of natural dawsonite occurrences, however, indicates that either appropriate CO2-rich environments are rare in nature or that dawsonite formation is inhibited or more complex than the simplified geochemical systems used in the model calculations. We have conducted synthesis experiments and dissolution studies to help understand precipitation dynamics, Na-K substitution, and solubility. Both Na- and K-dawsonite were readily synthesized from mixtures of (Na,K)HCO3 and gibbsite [Al(OH)3] at 150°C for 24 hours. [Syntheses were made in unstirred, closed ParrTM reaction vessels and consisted generally of 15 ml of H2O with 6 g (Na,K)HCO3 and sufficient Al-bearing mineral to achieve a (Na,K)/Al ratio of 8.] At lower temperatures, a 41% yield of dawsonite was achieved at 120°C; 1% at 94°C; and no reaction was observed at ≤75°C. In contrast, other Al-bearing minerals including albite, analcime and pyrophyllite at 150°C (28 days) and albite, pyrophyllite, and clinoptilolite at 200°C (66 days) showed no evidence of dawsonite formation but did yield analcime. Kaolinite, however, did produce 1% dawsonite at 75°C (40 days), 37% at 150°C (90 days), and some dawsonite in addition to a complex mixture of albite, cancrisilite, and other phases at 200°C (66 days). Thermodynamic calculations suggest that silica activity restricts the range of dawsonite stability and synthesis experiments with gibbsite-quartz and gibbsite-opal-CT were significantly different than gibbsite alone. At 150°C, the

  9. K-feldspar-quartz and K-feldspar-plagioclase phase boundary interactions in garnet-orthopyroxene gneiss's from the Val Strona di Omegna, Ivrea-Verbano Zone, northern Italy (United States)

    Harlov, Daniel E.; Wirth, Richard

    A detailed study based on textural observations combined with microanalysis [back scattered electron imaging (BSE) and electron microprobe analysis (EMPA)] and microstructural data transmission electron microscopy (TEM) has been made of K-feldspar micro-veins along quartz-plagioclase phase and plagioclase-plagioclase grain boundaries in granulite facies, orthopyroxene-garnet-bearing gneiss's (700-825°C, 6-8kbar) from the Val Strona di Omegna, Ivrea-Verbano Zone, northern Italy. The K-feldspar micro-veins are commonly associated with quartz and plagioclase and are not found in quartz absent regions of the thin section. This association appears to represent a localised reaction texture resulting from a common high grade dehydration reaction, namely: amphibole+quartz = orthopyroxene+clinopyroxene+plagioclase+K-feldspar+H2O, which occurred during the granulite facies metamorphism of these rocks. There are a number of lines of evidence for this. These include abundant Ti-rich biotite, which was apparently stable during granulite facies metamorphism, and total lack of amphibole, which apparently was not. Disorder between Al and Si in the K-feldspar indicates crystallisation at temperatures >500°C. Myrmekite and albitic rim intergrowths in the K-feldspar along the K-feldspar-plagioclase interface could only have formed at temperatures >500-600°C. Symplectic intergrowths of albite and Ca-rich plagioclase between these albitic rim intergrowths and plagioclase suggest a high temperature grain boundary reaction, which most likely occurred at the start of decompression in conjunction with a fluid phase. Relatively high dislocation densities (>2×109 to 3×109/cm2) in the K-feldspar suggest plastic deformation at temperatures >500°C. We propose that this plastic deformation is linked with the extensional tectonic environment present during the mafic underplating event responsible for the granulite facies metamorphism in these rocks. Lastly, apparently active garnet grain

  10. Bedout basement rise, offshore northwestern Australia: evidence of an unshocked mafic volcanic hyaloclastite volcanic breccia (United States)

    Glikson, A.


    Core samples from Bedout-1 (3035.8-3044.95 m.), Bedout basement rise, offshore northwestern Australia, were examined by optical microscopy, SEM, EDS and WDS spectrometry. At this stratigraphic depth level Becker et al. (2004) interpret cryptocrystalline alteration zones around and within plagioclase in terms of shock-induced transformation of feldspar into diaplectic maskelynite glass _u postulating a ~200 km-large impact structure and thereby an impact connection of the Permian-Triassic boundary mass extinction. However, the breccia is dominated by fragments of microlitic basalt and ophitic-textured dolerite with well preserved igneous textures, showing no evidence of shock metamorphism. Euhedral pseudomorphs of chlorite and amphibole, probably after pyroxene, protrude into or are enveloped by euhedral albite-twinned calcic plagioclase (andesine to bytownite). Minor phases include euhedral ilmenite needles and subhedral magnetite grains. Plagioclase is altered by cryptocrystalline albite and microcrystalline albite-chlorite matrix along crystal boundaries, along twin lamella and within internal oscillatory crystal zones, consistent with burial metamorphosed hydrovolcanic basalts and spilites (e.g. Amstutz, 1974). The volcanic fragments are set within, and injected by, microcrystalline intergranular mesostasis of mixed mineral fragments and volcanic meta-glass. Becker et al. (2004) refer to the breccia in part as product of Mg-rich sediments (e.g. dolomites). However, apart from the pristine igneous textures of the breccia, the transition element levels (chlorite in dolerite fragment "C Ni 97-160 ppm; Co 75-152 ppm; Cu 69-204 ppm; mesostasis "C Ni 29-45 ppm; Co 18-52 ppm; Cu 26-110 ppm) are consistent with Fe-rich basalts but exceed common abundances in carbonates and marls (BVTP, 1981; Wedepohl, 1978). No shock metamorphic features, such as planar deformation features (PDF), are observed in the feldspar or in any other phases. No criteria for discriminating

  11. The evolution of the Waiotapu geothermal system, New Zealand, based on the chemical and isotopic composition of its fluids, minerals and rocks (United States)

    Hedenquist, Jeffrey W.; Browne, Patrick R. L.


    The Waiotapu geothermal system is hosted by silicic rocks of the Taupo Volcanic Zone, New Zealand. Exploration drilling in the late 1950s down to 1100 m provided physical information on the system. Measured temperatures show a boiling profile to 295 °C, with shallow inversions, particularly in the north. Total discharge fluid samples were collected; the geothermometry and measured temperatures show that fluids derive mainly from a shallow (~400 m deep) reservoir at about 225°C. Petrologic study of drillcore samples recovered from seven wells reveals an alteration assemblage of quartz and albite + adularia, with a variable distribution of chlorite, pyrite, calcite, zeolites, epidote, pyrrhotite, sphene, leucoxene, apatite and minor base metal sulfides; white mica is a late overprint, particularly well developed at shallow depths. Surficial alteration of kaolin, cristobalite, alunite and smectite clays reflect alteration by acid sulfate, steam-heated waters. The activities of components in minerals (determined from microprobe analyses and composition-activity relations) and fluids (speciated to reservoir conditions) indicate equilibrium now exists between the fluids and white mica; the Na/K ratio of the fluid is being controlled by dissolution of albite and adularia, while its H 2/H 2S ratio is buffered by pyrite replacing pyrrhotite. The fluids are now slightly undersaturated with respect to calcite. The present deep fluids boil adiabatically from at least 300°C to 230°C; at depths of ≤500 m, this ascending chloride fluid is variably diluted by a steam-heated water (of zero chloride) that lies over, and occurs on the margin of, the system like a discontinuous umbrella; the steam-heated water is relatively CO 2-rich (≤0.1 m). The cooling at shallow levels by this mixing has shifted the alteration from albite-adularia stability to white mica stability; this shift is enhanced by the CO 2-rich nature of the diluent. Dilution of ascending chloride fluids by

  12. Thermoluminescent dependence with the particle size in ionized foods by radiation; Dependencia termoluminiscente con el tamano de particula en alimentos ionizados por radiacion

    Energy Technology Data Exchange (ETDEWEB)

    Teuffer Z, C.A


    The influence of the particle size of poly minerals in the signals of the thermally stimulated luminescence (TL) is analysed. The poly minerals were extracted of Mexican spices such as Origanum vulgare L. (origanum) and Capsicum annum (Chilli guajillo), these underwent to an homogenization process to obtain four different particle sizes corresponding to 149, 74, 53 and 10 {mu} m, and later on to expose them to gamma radiation in an interval of 0.5- 45 kGy in the Gamma beam 651 PT of {sup 60} Co irradiator of the Nuclear Sciences Institute, UNAM. The glow curves show a maximum of TL intensity for Capsicum annum to dose of 0.5- 10 kGy with particle size selected by means of a mesh of opening of 53 {mu} m, while for Origanum vulgare L., the more intense emission is observed with 149 {mu} m. In the interval of dose 12- 45 kGy the maximum in intensity emission it was presented in 53 {mu} m in both cases. For the case of 10 {mu} m, the TL emissions were of smaller intensity, and were achieved glow curves in a clear, defined way and an overlapping that allows to center the maximum of TL emission, in a defined temperature 126 C for Origanum vulgare L., and 166 C for Capsicum annum. The behavior before described is related with the composition of the samples. For Capsicum annum it was found Quartz (60%), Albite (30%) and Ortosa (10%), while Origanum vulgare stops L., Quartz (50%), Calcite (20%), Albite (20%) and Clay (10%). The homogenization of the samples is an important factor because exists high probability of avoiding as much as possible rests of organic matter traces that can contribute to the total signal of the glow curves. Likewise the defects that pollute from a natural way to each one of the minerals found in the samples, they play an outstanding role in the TL emissions. Although to the interacting the gamma radiation with the poly minerals of different particle sizes, there is a certain energy transfer that will be translated in the absorbed dose and this it

  13. Nature, origin and evolution of the granitoid-hosted early Proterozoic copper-molybdenum mineralization at Malanjkhand, Central India (United States)

    Sarkar, S. C.; Kabiraj, S.; Bhattacharya, S.; Pal, A. B.


    At Malanjkhand, Central India, lode-type copper (-molybdenum) mineralization occurs within calcalkaline tonalite-granodiorite plutonic rocks of early Proterozoic age. The bulk of the mineralization occurs in sheeted quartz-sulfide veins, and K-silicate alteration assemblages, defined by alkali feldspar (K-feldspar≫albite)+dusty hematite in feldspar±biotite±muscovite, are prominent within the ore zone and the adjacent host rock. Weak propylitic alteration, defined by albite+biotite+epidote/zoisite, surrounds the K-silicate alteration zone. The mineralized zone is approximately 2 km in strike length, has a maximum thickness of 200 m and dips 65° 75°, along which low-grade mineralization has been traced up to a depth of about 1 km. The ore reserve has been conservatively estimated to be 92 million tonnes with an average Cu-content of 1.30%. Supergene oxidation, accompanied by limited copper enrichment, is observed down to a depth of 100 m or more from the surface. Primary ores consist essentially of chalcopyrite and pyrite with minor magnetite and molybdenite. δ34S (‰) values in pyrite and chalcopyrite (-0.38 to +2.90) fall within the range characteristic of granitoid-hosted copper deposits. δ18O (‰) values for vein quartz (+6.99 to +8.80) suggest exclusive involvement of juvenile water. Annealed fabrics are common in the ore. The sequence of events that led to the present state of hypogene mineralization is suggested to be as follows: fracturing of the host rock, emplacement of barren vein quartz, pronounced wall-rock alteration accompanied by disseminated mineralization and the ultimate stage of intense silicification accompanied by copper mineralization. Fragments of vein quartz and altered wall rocks and striae in the ore suggest post-mineralization deformation. The recrystallization fabric, particularly in chalcopyrite and sphalerite, is a product of dynamic recrystallization associated with the post-mineralization shearing. The petrology of the host

  14. Mineralogy and geochemistry of a superhigh-organic-sulfur coal, Yanshan Coalfield, Yunnan, China: Evidence for a volcanic ash component and influence by submarine exhalation (United States)

    Dai, S.; Ren, D.; Zhou, Y.; Chou, C.-L.; Wang, X.; Zhao, L.; Zhu, Xudong


    The mineralogy and geochemistry of a superhigh-organic-sulfur (SHOS) coal of Late Permian age from the Yanshan Coalfield, Yunnan Province, southwestern China, have been studied using optical microscope, low-temperature ashing plus X-ray diffraction analysis, scanning electron microscope equipped with energy-dispersive X-ray spectrometer, a sequential chemical extraction procedure, and inductively coupled plasma mass spectrometry. The M9 Coal from the Yanshan Coalfield is a SHOS coal that has a total sulfur content of 10.12%-11.30% and an organic sulfur content of 8.77%-10.30%. The minerals in the coal consist mainly of high-temperature quartz, sanidine, albite, muscovite, illite, pyrite, and trace amounts of kaolinite, plagioclase, akermanite, rutile, and dawsonite. As compared with ordinary worldwide (bituminous coals and anthracite) and Chinese coals, the M9 Coal is remarkably enriched in B (268????g/g), F (841????g/g), V (567????g/g), Cr (329????g/g), Ni (73.9????g/g), Mo (204????g/g), and U (153????g/g). In addition, elements including Se (25.2????g/g), Zr (262????g/g), Nb (20.1????g/g), Cd (2.07????g/g), and Tl (2.03????g/g) are also enriched in the coal. Occurrence of high-temperature quartz, sanidine, muscovite, and illite in the M9 Coal is evidence that there is a volcanic ash component in the coal that was derived from acid volcanic ashes fallen into the swamp during peat accumulation. Occurrence of albite and dawsonite in the coal and strong enrichment of some elements, including F, S, V, Cr, Ni, Mo and U, are attributed to the influence by submarine exhalation which invaded along with seawater into the anoxic peat swamp. Abundances of lithophile elements, including rare earth elements, Nb, Y, Zr, and TiO2, indicate that the silicate minerals in the coal were derived from the northern Vietnam Upland to the south of the basin. ?? 2008 Elsevier B.V. All rights reserved.

  15. Theoretical prediction for several important equilibrium Ge isotope fractionation factors (United States)

    Tang, M.; Li, X.; Liu, Y.


    As a newly emerging field, the stable isotope geochemistry of germanium (Ge) needs basic equilibrium fractionation factors to explore its unknown world. In this study, the Ge isotope fractionations between systems including the aqueous Ge(OH)4 and GeO(OH)3- which are the dominant Ge species in seawater, the Ge-bearing organic complexes (e.g. Ge-catechol, Ge-oxalic acid and Ge-citric acid), the quartz- (or opal- ), albite-, K-feldspar- and olivine- like mineral structures are studied. It is the first time that some geologically important equilibrium Ge isotope fractionation factors are reported. Surprisingly, up to 5 per mil large isotopic fractionations between these Ge isotope systems are found at 25 degree. These results suggest a potentially broad application for the Ge isotope geochemistry. Our theoretical calculations are based on the Urey model (or Bigeleisen-Mayer equation) and high level quantum chemistry calculations. The B3LYP/6-311+G(d,p) level quantum chemistry method and the explicit solvent model ("water droplet" method) are used. Many different conformers are also used for the aqueous complexes in order to reduce the possible errors coming from the differences of configurations in solution. The accuracy of our calculation of the Ge isotopic fractionations is estimated about 0.2 per mil. Our results show quartz-like or opal-like structure can enrich most heavy Ge isotopes. Relative to quartz (or opal), some Ge isotopic fractionations are (at 25 C): quartz-organic Ge = 4-5,quartz-Ge(OH)4 =0.9,quartz-GeO(OH)3- =1.5,quartz-albite=0.6,quartz-K-feldspar=0.4 and quartz-olivine=3.9 per mil. The large fractionations between inorganic Ge complexes and organic Ge ones could be used to distinguish the possible bio-involving processes. Our results suggest a good explanation to the experimental observations of Siebert et al. (2006) and Rouxel et al. (2006) and provide important constraints to the study of Ge cycle in ocean.

  16. Late Paleozoic onset of subduction and exhumation at the western margin of Gondwana (Chilenia Terrane): Counterclockwise P-T paths and timing of metamorphism of deep-seated garnet-mica schist and amphibolite of Punta Sirena, Coastal Accretionary Complex, central Chile (34° S) (United States)

    Hyppolito, T.; García-Casco, A.; Juliani, C.; Meira, V. T.; Hall, C.


    In this study, the Paleozoic albite-epidote-amphibolite occurring as meter-sized intercalations within garnet-mica schist at Punta Sirena beach (Pichilemu region, central Chile) is characterized for the first time. These rocks constitute an unusual exposure of subduction-related rocks within the Paleozoic Coastal Accretionary Complex of central Chile. Whereas high pressure (HP) greenschist and cofacial metasediments are the predominant rocks forming the regional metamorphic basement, the garnet-mica schist and amphibolite yield higher P-T conditions (albite-epidote amphibolite facies) and an older metamorphic age. Combining detailed mineral chemistry and textural information, P-T calculations and Ar-Ar ages, including previously published material from the Paleozoic Accretionary Complex of central Chile, we show that the garnet-mica schist and associated amphibolite (locally retrograded to greenschist) are vestiges of the earliest subducted material now forming exotic bodies within the younger HP units of the paleo-accretionary wedge. These rocks are interpreted as having been formed during the onset of subduction at the southwestern margin of Gondwana. However, we show that the garnet-mica schist formed at a slightly greater depth (ca. 40 km) than the amphibolite (ca. 30 km) along the same hot-subduction gradient developed during the onset of subduction. Both lithotypes reached their peak-P conditions at ca. 335-330 Ma and underwent near-isobaric cooling followed by cooling and decompression (i.e., counterclockwise P-T paths). The forced return flow of the garnet-mica schist from the subduction channel started at ca. 320 Ma and triggered the exhumation of fragments of shallower accreted oceanic crust (amphibolite). Cores of phengite (garnet-mica schist) and amphibole (amphibolite) grains have similar chemical compositions in both the S1 and S2 domains, indicating rotation of these grains during the transposition of the burial-related (prograde peak-T) foliation S1

  17. Chemical mobility during low-grade metamorphism of a Jurassic lava flow: Río Grande Formation, Peru (United States)

    Aguirre, L.

    Chemical and mineralogical changes produced by very low-grade metamorphism in a 40 meter thick, K-rich, calc-alkaline andesite flow of the marine Jurassic Río Grande Formation of southern coastal Peru are discussed. This metamorphism (=spilitization) was non-deformational and generated spilitic domains at (and near) both vesicular margins of the flow, whereas the massive central zone remained relatively unaltered. The metadomains are characterized by mineral associations of the zeolite facies. Primary minerals are Ca-plagioclase, augitic pyroxene, iron-titanium oxides, and (pseudomorphs after) olivine. Metamorphic minerals are: albite (three generations), K-feldspar, pumpellyite, chlorite, interlayered chlorite-celadonite, celadonite, various mixed-layer Si- and Fe-rich phyllosilicates, "iddingsite," calcite, analcime, titanite, and white mica. The effect of the metamorphism on the rock chemistry is reflected in changes especially observed at the marginal zones of the flow which affect major, trace, and RE elements: 1) strong increase of the iron oxidation ratio (Fe 2O 3/FeO); 2) enrichment in Na 2O accompanied by a concomitant depletion of CaO in non-amygdaloidal domains; 3) depletion of SiO 2; 4) strong enrichment in H 2O and CO 2; 5) marked depletion of Sr and Rb; 6) enrichment in Cl and S; and 7) slight depletion in RE elements, notably in the top zone of the flow. Conversely, elements such as Ti, P, Nb, and Y were fairly immobile, whereas Zr and K were only slightly mobilized. The effect of the metamorphism on the mineral chemistry is expressed by the predominance of metastable equilibrium evidenced by the existence of wide compositional ranges in the phyllosilicates, the incomplete albitization of the Ca-plagioclase, and the Al-rich character of the pumpellyites. The metamorphism is considered to be of hydrothermal-burial type, which takes place at low temperature and pressure — probably about 125-230°C and less than 3 kb, and is produced mainly through

  18. Compositional characteristics and Existing Forms of Major,Trace and Rare—earth Elements in Cassiterite,Dupangling Tin Ore Field,Guangxi

    Institute of Scientific and Technical Information of China (English)

    干国梁; 陈志雄


    Trace elements in cassiterite,including Ta,W,Fe,Mn,Ti,Zr,V,Sc,Si,Al,In,Ga,Ge,Be,Bi,Ag,Sb,As,Cu,Pb,Zn,Co and REE,have been studied by many workers (Shan Zhenhua etal.,1998;Huang Zhou Tianren et al.,1987;Wu Qingsheng et al.,1988;Hu Zening,1988,Li Zhong-qing 1988 Mingzhei et al.,1988;Wang Lihua et al.,1988;Liu Kanghuai,1990).Up to now,however,most of the previous studies are concerned with trace-element variations in cassiterites of different occurrences and colors from different types of ore deposits,Data concerning the modes of occurrence of these trace elements are rare,except for the contention that Nb-Ta,Fe2+-Mn-Fe3+ and W-Fe3+ may substitute isomorphously for Sn as pointed out by Zhou Tianren et al.(1987) and Moller et al.(1988).In this paper we are concerned with the compositional characteristics as well as the modes of occurrence of trace elements in cassiterites from quartz veins and greisens in the Dupangling tin field,Guangxi,based on multivariate statistical analyses.Tin mineralization in the Dupangling area is found associated with the medium-to fine-grained protolithionite-albite granite(γ52b) and its outer contacts.Cassiterite occurs,with wolframite,both in quartz veins in the contact and in greisens within the granite.1) Spatially,greisens become dominant over quartz veins in the contact andin greisens with the granite.1)Spatialy,gresens become dominant over quartz veins in going from the contact to the interior of the granite and with increasing depth.The greisens are of various shapes.The vein-shaped and the sheet-shaped greisens at the top of the granie are rich in quartz and the chambered greiens always constitute rich ores and contain abundant topaz or mica.Genetically,Sn,W mineralizations associated with the protolithionite-albite granite(γ52b) are considered to have been formed from fluid melt derived from the ore-forming magma responsible for the granite(γ52b).

  19. Mineral replacement reactions and element mobilization (United States)

    Putnis, Christine V.; Ruiz-Agudo, Encarnacion; King, Helen E.; Hövelmann, Jörn; Renard, François


    When a mineral is out of equilibrium with an aqueous fluid, reactions will take place in an attempt to reach a new equilibrium. Commonly in the Earth dissolution at a mineral-fluid interface initiates a coupled reaction involving dissolution and precipitation (Ruiz-Agudo et al., 2014). This is a ubiquitous reaction during such processes as metamorphism, metasomatism and weathering. When rock-forming minerals such as feldspars, olivine, pyroxenes are in contact with aqueous fluids (typically NaCl-rich) resultant new phases are formed and elements present in the parent mineral are released to the fluid and therefore mobilized for transport elsewhere. This has been shown in a number of systems such as the albitisation of feldspars (Hövelmann et al., 2010) when a Ca-bearing plagioclase is replaced by albite (NaAlSi3O8). However during this reaction not only is Ca released to the fluid but most other minor elements, such as Mg, Pb, rare earth elements amongst others, are almost totally mobilized and removed in solution. This interface-coupled dissolution-precipitation reaction has many implications for the redistributon of elements in the crust of the Earth. It is also of note that albitisation occurs often in areas of high mineralization, such as in the Curnamona Province in S. Australia (Au-Cu and Ag-Pb-Zn deposits) and the Bamble District of S. Norway. Secondly atomic force microscopy (AFM) has been used to image these reactions at a nanoscale, especially at the calcite-fluid interface, such as the formation of apatite from phosphate-bearing solutions, and the sequestration of toxic elements, eg., Se and As. References Ruiz-Agudo E., Putnis C.V., Putnis A. (2014) Coupled dissolution and precipitation at mineral-fluid interfaces. Chemical Geology, 383, 132-146. Putnis C.V. and Ruiz-Agudo E. (2013) The mineral-water interface: where minerals react with the environment. Elements, 9, 177-182. Hövelmann J., Putnis A., Geisler T., Schmidt B.C., Golla-Schindler U. (2009

  20. Can the dissolution rates of individual minerals be used to describe whole rock dissolution? (United States)

    Critelli, Teresa; Marini, Luigi; Schott, Jacques; Mavromatis, Vasileios; Apollaro, Carmine; Rinder, Thomas; De Rosa, Rosanna; Oelkers, Eric H.


    There have been an exhaustive number of laboratory studies determining the dissolution rates of individual minerals, but few have focused on the dissolution rates of minerals in multi-mineralic rocks. As a result, geochemical modeling of the temporal evolution of water-rock interaction is generally based on the assumption that the dissolution rate of minerals within a rock is equal to that measured in the laboratory on individual minerals. To verify this hypothesis, we have determined experimentally the dissolution rates of a well characterized metabasalt rock (Apollaro et al., 2011; Bloise et al., 2012) from the Mt. Reventino area (Southern Italy) at 25°C in mixed flow reactors. From these experiments and rock modal analysis we have deduced the dissolution rates of the minerals present in the rock (actinolite, albite, chlorite, epidote, and phengite). The major observation of this effort include: (i) only small differences in the dissolution rates of the individual minerals were observed; these rates are close to the whole-rock dissolution rate and (ii) the dissolution rates of albite and chlorite are in close agreement with laboratory rates obtained from individual mineral dissolution experiments, whereas those of actinolite, phengite, and epidote are not consistent with those reported in literature by 1-2 orders of magnitude. These results demonstrate that the dissolution rate of a given mineral in a multi-phase rock can be affected by the presence of the other minerals. Rock dissolution kinetics are likely constrained by the dissolution rates of the more abundant, lesser reactive mineral or minerals in the rock. These unreactive minerals can prevent the dissolution of the more rapidly dissolving mineral grains by keeping them out of contact with the aqueous phase. This implies that the overall weathering rate of rocks cannot be modelled from the measured dissolution rates of its individual minerals. If confirmed through further studies, this conclusion may

  1. Hydrofracturing of Sediment and Hydrated MORB's during Subduction of Ocean Crust (United States)

    Nabelek, P. I.


    Dehydration accompanying metamorphism of sediment and hydrated mafic ocean crust during ocean plate subduction can potentially lead to fracturing and intraplate tremors. As rocks are buried, they lose porosity and permeability and eventually pass into the lithostatic pressure regime where the porosity and permeability are thought to be very small. Pore fluid pressure generation stemming from metamorphic reactions was modeled using the program SUTRAMET (Nabelek et al., 2014), which is a modified version of the program SUTRA (Voss & Provost, 2002). The program allows modeling of metamorphic reactions at high pressures and temperatures and incorporates transient porosity and permeability changes due to overpressure and changing volumes of metamorphic assemblages. Permeabilities (k) of 10-18 and 10-20 m2 within the brittle regime were modeled. The model assumes continuous subduction with fluids generated at horizons where specific P-T conditions for reactions exist. Temperature gradient was assumed to be 10°C/km and the vertical component of subduction velocity to be at 0.85 cm/y. The model reactions in sediment (Campito Formation of western California as a proxy) and average MORB were generated by the program Theriak-Domino (de Capitani and Petrakakis, 2010). The initial sediment mineralogy includes albite, K-feldspar, phengite, chlorite, and lawsonite. The final mineralogy for the 10°C/km gradient is quartz, phengite, garnet, and pyroxene with jadeite and acmite components. The initial mineralogy of MORB includes chlorite, amphibole, pumpelyite, albite and quartz and the final eclogite mineralogy includes garnet, cpx, kyanite and quartz. Calculations show that at k = 10-18 m2, pore fluid pressure can reach 450 MPa. Pore pressure is reduced by negative ∆V of mineral assemblages stemming from reactions; nevertheless, for the garnet-forming reaction, pore pressure is about 110 MPa. Assuming a tensile strength of 15 MPa and fracture aperture given by rock

  2. Episyenites in meta-granitoids of the Tauern Window (Eastern Alps): unpredictable? (United States)

    Pennacchioni, Giorgio; Ceccato, Alberto; Fioretti, Anna Maria; Mazzoli, Claudio; Zorzi, Federico; Ferretti, Patrizia


    The core of the Tauern tectonic window (Eastern Alps) consists of pre-Alpine granitoids (∼295 Ma) variably deformed during Alpine (∼30 Ma) amphibolite-facies metamorphism. Episyenites occur as local alteration haloes (as wide as a few meters) surrounding steeply dipping, strike-slip faults, with offsets meta-granodiorite) and 13% (meta-aplite), mainly derived from dissolution of quartz. Glacier-polished outcrops allow the detailed investigation of the relationships between the episyenites and the structure of the associated faults. Field mapping indicates that episyenites: (i) are spatially linked to pre-existing faults and statically overprinted these structures; (ii) are discontinuous along faults; (iii) have a thickness (of as much as a few meters) that does not correlate with either the amount of slip along the pre-existing faults or the spatial density of the fracture network; (iv) developed with a similar extent in rocks with conspicuous variations of the original quartz grain size and structure. The studied outcrop includes a relatively large volume of episyenite associated with faults. However, despite the pervasiveness of faulting, episyenites are rare in the Tauern meta-granitoids. This localized occurrence of episyenite is inferred to represent a section of a vertical pipe structure exploiting a portion of the fault network. Our study indicates that the location and the extent of episyenite alteration cannot be simply predicted from the geometry and the fracturing patterns of the pre-existing cataclastic faults. Quartz dissolution during episyenitization was accompanied and/or followed by: (i) pervasive substitution of oligoclase and biotite/chlorite of the meta-granodiorite by albite and vermicular chlorite, respectively; and (ii) precipitation of adularia, albite, anatase, calcite, hematite and zeolites within pores. Isotopic data from the calcite filling of the pores suggest a surficial source of fluids associated with this calcite precipitation

  3. Paleoproterozoic volcanic centers of the São Félix do Xingu region, Amazonian craton, Brazil: Hydrothermal alteration and metallogenetic potential (United States)

    da Cruz, Raquel Souza; Fernandes, Carlos Marcello Dias; Villas, Raimundo Netuno Nobre; Juliani, Caetano; Monteiro, Lena Virgínia Soares; Lagler, Bruno; Misas, Carlos Mario Echeverri


    Geological, petrographic, scanning electron microscopy, and X-ray diffraction studies revealed hydrothermalized lithotypes evidenced by overprinted zones of potassic, propylitic, sericitic, and intermediate argillic alterations types, with pervasive and fracture-controlled styles, in Paleoproterozoic volcano-plutonic units of the São Félix do Xingu region, Amazonian craton, northern Brazil. The Sobreiro Formation presents propylitic (epidote + chlorite + carbonate + clinozoisite + sericite + quartz ± albite ± hematite ± pyrite), sericitic (sericite + quartz + carbonate), and potassic (potassic feldspar + hematite) alterations. The prehnite-pumpellyite pair that is common in geothermal fields also occurs in this unit. The Santa Rosa Formation shows mainly potassic (biotite + microcline ± magnetite), sericitic (sericite + quartz + carbonate ± chlorite ± gold), and intermediate argillic (montmorillonite + kaolinite/halloysite + illite) alterations. These findings strongly suggest the involvement of magma-sourced and meteoric fluids and draw attention to the metallogenetic potential of these volcanic units for Paleoproterozoic epithermal and rare and base metal porphyry-type mineralizations, similar to those already identified in other portions of the Amazonian craton.

  4. The geomicrobiology of bauxite deposits

    Directory of Open Access Journals (Sweden)

    Xiluo Hao


    Full Text Available Bauxite deposits are studied because of their economic value and because they play an important role in the study of paleoclimate and paleogeography of continents. They provide a rare record of the weathering and evolution of continental surfaces. Geomicrobiological analysis makes it possible to verify that microorganisms have played a critical role during the formation of bauxite with the possibility already intimated in previous studies. Ambient temperature, abundance of water, organic carbon and bioavailable iron and other metal substrates provide a suitable environment for microbes to inhabit. Thiobacillus, Leptospirilum, Thermophilic bacteria and Heterotrophs have been shown to be able to oxidize ferrous iron and to reduce sulfate-generating sulfuric acid, which can accelerate the weathering of aluminosilicates and precipitation of iron oxyhydroxides. Microorganisms referred to the genus Bacillus can mediate the release of alkaline metals. Although the dissimilatory iron-reducing and sulfate-reducing bacteria in bauxites have not yet been identified, some recorded authigenic carbonates and “bacteriopyrites” that appear to be unique in morphology and grain size might record microbial activity. Typical bauxite minerals such as gibbsite, kaolinite, covellite, galena, pyrite, zircon, calcium plagioclase, orthoclase, and albite have been investigated as part of an analysis of microbial mediation. The paleoecology of such bauxitic microorganisms inhabiting continental (sub surfaces, revealed through geomicrobiological analysis, will add a further dimension to paleoclimatic and paleoenvironmental studies.

  5. Kumdykolite, kokchetavite, and cristobalite crystallized in nanogranites from felsic granulites, Orlica-Snieznik Dome (Bohemian Massif): not an evidence for ultrahigh-pressure conditions (United States)

    Ferrero, Silvio; Ziemann, Martin A.; Angel, Ross J.; O'Brien, Patrick J.; Wunder, Bernd


    A unique assemblage including kumdykolite and kokchetavite, polymorphs of albite and K-feldspar, respectively, together with cristobalite, micas, and calcite has been identified in high-pressure granulites of the Orlica-Snieznik dome (Bohemian Massif) as the product of partial melt crystallization in preserved nanogranites. Previous reports of both kumdykolite and kokchetavite in natural rocks are mainly from samples that passed through the diamond stability field. However, because the maximum pressure recorded in these host rocks is <3 GPa, our observations indicate that high pressure is not required for the formation of kumdykolite and kokchetavite, and their presence is not therefore an indicator of ultrahigh-pressure conditions. Detailed microstructural and microchemical investigation of these inclusions indicates that such phases should instead be regarded as (1) a direct mineralogical criteria to identify former melt inclusions with preserved original compositions, including H2O and CO2 contents and (2) indicators of rapid cooling of the host rocks. Thus, the present study provides novel criteria for the interpretation of melt inclusions in natural rocks and allows a more rigorous characterization of partial melts during deep subduction to mantle depth as well as their behavior on exhumation.

  6. Geothermal System as the Cause of the 1979 Landslide Tsunami in Lembata Island, Indonesia

    Directory of Open Access Journals (Sweden)

    Yudhicara Yudhicara


    Full Text Available DOI:10.17014/ijog.2.2.91-99A tsunami landslide which caused hundreds casualties and lots of damage took place on Lembata Island in 1979. In order to understand the characteristics of the landslide mechanism, a field survey was conducted in 2013 which sampled both the origin soil and landslide material, and the water from hotspring around the landslide site. The physical properties of the soil obtained show that the original soil has dominantly coarser grain than the landslide material (80.5% coarser grain compared to 11.8% coarse grain respectively which indicates that the soil has become finer and softer. Hot spring analysis indicated that the mineral content of the water was 99.48% SO4. This shows that magmatism processes are involved which caused the soil to become acidic and may have fragilised the system. Results of X-ray Diffraction Mineralogy Analysis (XRD show that the original soil is composed of minerals of cristobalite, quartz, and albite, while the landslide material consists of clay minerals such as quartz, saponite, chabazite, silicon oxide, and coesite which are typical minerals in a hydrothermal environment. Based on these results, it can be concluded that the area was influenced by an active geothermal system that could be the main source mechanism behind this disastrous event. 

  7. Microstructural, modal and geochemical changes as a result of granodiorite mylonitisation – a case study from the Rolovská shear zone (Čierna hora Mts, Western Carpathians, Slovakia

    Directory of Open Access Journals (Sweden)

    Farkašovský Roman


    Full Text Available Strong tectonic remobilisation and shear zone development are typical features of the easternmost part of the Veporicum tectonic unit in the Western Carpathians. The granodiorite mylonites in the area of the Rolovská shear zone (Čierna hora Mts underwent a complex polystage evolution during the Hercynian and Alpine orogenies. Deformation during the latter reached greenschist facies under metamorphic conditions. Mylonites are macroscopically foliated rocks with a stretching lineation and shear bands. Structurally different mylonite types, ranging from protomylonites to ulramylonites with typical grainsize reduction from the margins towards the shear zone centre, have been assessed. The modal mineralogy of the different mylonite types changes considerably. Typical is a progressive decrease in feldspar content and simultaneously the quartz and white mica content increases from protomylonites towards the most strongly deformed ultramylonites. The deformation had a brittle character in less deformed rocks and a ductile one in more deformed tectonites. Obvious chemical changes occur in mesomylonites and ultramylonites. During mylonitisation, the original biotite granodiorite was depleted of Mg, Fe, Na, Ca and Ba, while K, Rb and mainly Si increased considerably. Other (major and trace elements reflect erratic behaviour due to lateral mobility. Chemical changes indicate the breakdown and subsequent recrystallisation of biotite and feldspars and, in turn, the crystallisation of albite and sericite. REE decrease in ultramylonites due to the breakup of accessory minerals during deformation and alteration.

  8. Study on the enhancement of hydrocarbon recovery by characterization of the reservoir

    Energy Technology Data Exchange (ETDEWEB)

    Jeong, Tae-Jin; Kwak, Young-Hoon; Huh, Dae-Gee [Korea Institute of Geology Mining and Materials, Taejon (KR)] (and others)


    The reservoir geochemistry is to understand the origin of these heterogeneities and distributions of the bitumens within the reservoir and to use them not only for exploration but for the development of the petroleums. Methods and principles of the reservoir geochemistry, which are applicable to the petroleum exploration and development, are reviewed in the study. In addition, a case study was carried out on the gas, condensate, water and bitumen samples in the reservoir, taken from the Haenam, Pohang areas and the Ulleung Basin offshore Korea. Mineral geothermometers were studied to estimate the thermal history in sedimentary basins and successfully applied to the Korean onshore and offshore basins. The opal silica-to-quartz transformation was investigated in the Pohang basin as a geothermometer. In Korean basins, the smectite-to-illite changes indicate that smectite and illite can act as the geothermometer to estimate the thermal history of the basins. The albitization reaction was also considered as a temperature indicator. Naturally fractured reservoir is an important source of oil and gas throughout the world. The properties of matrix and fracture are the key parameters in predicting the performances of naturally fractured reservoirs. A new laboratory equipment has been designed and constructed by pressure pulse method to determine the properties, which are (1) the porosity of matrix, (2) the permeability of matrix, (3) the effective width of the fractures, and the permeability of the fractures. (author). 97 refs.

  9. The geomicrobiology of bauxite deposits

    Institute of Scientific and Technical Information of China (English)

    Xiluo Hao; Kwunlun Leung; Rucheng Wang; Weidong Sun; Yiliang Li


    Bauxite deposits are studied because of their economic value and because they play an important role in the study of paleoclimate and paleogeography of continents. They provide a rare record of the weathering and evolution of continental surfaces. Geomicrobiological analysis makes it possible to verify that microorganisms have played a critical role during the formation of bauxite with the possibility already intimated in previous studies. Ambient temperature, abundance of water, organic carbon and bioavailable iron and other metal substrates provide a suitable environment for microbes to inhabit. Thiobacillus, Leptospirilum, Thermophilic bacteria and Heterotrophs have been shown to be able to oxidize ferrous iron and to reduce sulfate-generating sulfuric acid, which can accelerate the weathering of aluminosilicates and precipitation of iron oxyhydroxides. Microorganisms referred to the genus Bacillus can mediate the release of alkaline metals. Although the dissimilatory iron-reducing and sulfate-reducing bacteria in bauxites have not yet been identified, some recorded authigenic carbonates and "bacteriopyrites" that appear to be unique in morphology and grain size might record microbial activity. Typical bauxite minerals such as gibbsite, kaolinite, covellite, galena, pyrite, zircon, calcium ptagioclase, orthoclase, and albite have been investigated as part of an analysis of microbial mediation. The paleoecologyof such bauxitic microorganisms inhabiting continental (sub) surfaces, revealed through geomicrobiological analysis, will add a further dimension to paleoclimatic and paleoenvironmental studies.

  10. Sludge granulation and efficiency of phase separator in UASB reactor treating combined industrial effluent. (United States)

    Yasar, Abdullah; Ahmad, Nasir; Chaudhry, Muhammad Nawaz; Khan, Aamir Amanat Ali


    Sludge granulation and the effect of gas-liquid-solid separator (GLSS) design on the efficiency of upflow anaerobic sludge blanket (UASB) and upflow anaerobic sludge filter (UASF) reactors, operating at HRTs ranging from 3 to 12 h were investigated. VSS/TS ratio gradually increased in both the reactors with increasing sludge age (from 0.5 to more than 0.7 for UASB reactor and 0.012 to 0.043 for UASF reactor). X-Ray diffraction analysis of the UASF sludge showed the presence of expanding clays revealing its additional absorption capability. Fuoraphyllite and albite precipitation related to excellular polymers of the microbial shell structure, showed the extended growth of microorganisms during sludge granulation. A gradual decrease (82%-69%) in COD removal with decreasing HRT was apparent in UASF reactor. In case of UASB reactor, this decrease was marginal because addition of GLSS device significantly improved (14%-20%) the overall efficiency of the UASB reactor. GLSS enhanced the efficiency of the UASB reactor by increasing the settleability of suspended particles and accelerating the coagulation of colloidal particles due to the velocity gradient.

  11. U-Pb ages related to uranium mineralization of Lagoa Real, Bahia - Brazil: tectonic implications

    Energy Technology Data Exchange (ETDEWEB)

    Chaves, Alexandre O.; Rios, Francisco J.; Oliveira, Lucilia A.R.; Alves, James V.; Fuzikawa, Kazuo; Neves, Jose M.C.; Chaves, Adriana M.D.V.; Prates, Sonia P. [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)]. E-mail:; Tubrett, Michael [Memorial University of Newfoundland, NL (Canada). Inco Innovation Centre. MicroAnalysis Facility; Matos, Evando C. [Industrias Nucleares do Brasil S.A. (INB), Rio de Janeiro, RJ (Brazil)


    The uranium from Lagoa Real (Bahia/Brazil) is associated with syenitic magmatism (1904 {+-}44 Ma minimum age from upper intercept of zircon U-Pb discordia by LA-ICP-MS) belonging to a mafic/ felsic lithologic association linked to the final stages of 2.05-1.80 Ga Orosirian Orogeny, which acted in the Paramirim Block. These syenitic rocks are rich not only in albite, but also in U-rich titanite (source of uranium). In association with the development of the Orosirian ductile shear zones, the syenites were crystallized and deformed. The metamorphic reactions, which include intense recrystallization of magmatic minerals, led uraninite to precipitate (1868 {+-} 69 Ma; U-Pb by LA-ICP MS) under Redox control. A second population of uraninites was also generated by shear zones reactivation during 0.6-0.5 Ga Brasiliano Orogeny (605 {+-} 170 Ma; U-Pb by LA-ICP-MS). The geotectonic implications are: a) the importance of the Orosirian event in the Paramirim Block during paleoproterozoic Sao Francisco/Congo Craton edification and b) the influence of the Brasiliano event in the Paramirim Block during the West-Gondwana assembly processes, indicated by the 605 {+-} 170 Ma uraninite (second population) age and by the 483 {+-} 100 Ma lower intercept of the metamorphosed syenite U-Pb discordia. (author)

  12. Use of a cranium-vessel determined by means of compound analysis; Uso de una vasija-craneo determinada por medio de analisis de compuesto

    Energy Technology Data Exchange (ETDEWEB)

    Leboreiro, I.; Pijoan, C.M.; Mansilla, J. [Direccion de Antropologia Fisica, INAH, Gandhi s/n, Polanco, 11560 Mexico D. F. (Mexico); Bosch, P. [Instituto de Investigaciones en Materiales, UNAM, Circuito Exterior, Ciudad Universitaria, 04510 Mexico D. F. (Mexico)


    Many human remains as bones, skin, teeth and others, were used in pre-hispanic cultures as tools or ritual objects. A human cranial vault filed in the Direccion de Antropologia Fisica presented particular and interesting cultural modifications. There are twelve drills used to restore by sewing the crane, in this way the piece resembles a pot. It has been established that it comes from North Mexico where such restoration work has been reported (Aveleyra, 1956) for containers made of vegetables (guaje). As the utilization of this kind of archaeological remain is unknown, the study of dust samples from the inside and the outside of the crane should provide hints on the products stored into it. In this study we present the X-ray diffraction results which show that the outer dusts are mainly constituted by albite, andesite and quartz, whereas in the inside the substances were mainly aluminosilicates and magnesium compounds. Hence, most probably, this crane was not used as a conventional container and it is linked to the concoction of magnesium and aluminosilicates containing products. This conclusion has to be correlated to that even nowadays, in both alternative and conventional medicine. (Author) 7 refs., 7 figs.

  13. NaAlSi3O8-hollandite and other high-pressure minerals in the shock melt veins of the Suizhou meteorite

    Institute of Scientific and Technical Information of China (English)


    The Suizhou L6 chondrite contains a few very thin shock melt veins of 0.02-0.09 mm in width. In spite of small width of the veins, shock-induced high-pressure phases, such as coarse-grained NaAlSi3O8-hollandite, ringwoodite, majorite and fine-grained matrix majorite-pyropess have been discovered in these veins. NaAlSi3O8-hollandite, the high-pressure phase of plagioclase, in Suizhou shock veins occurs as a single phase mineral, no silicate glassy phase, such as albitic glass, was incorporated with it. The presence of above-mentioned high-pressure phases constrains the high pressure (up to 23-24 GPa) and high temperature (up to 1900-2000℃) regime in Suizhou shock veins, and indicates that the duration of high-pressure regime in the veins should be long enough (a few seconds) for phase transformation and crystallization of minerals under pressure. The discovery of the first natural single-phase crystalline NaAlSi3O8- hollan-dite in Suizhou meteorite is of important significance in un-derstanding the Earth's mantle geochemistry.

  14. Protolith age of Santa Maria Chico granulites dated on zircons from an associated amphibolite-facies granodiorite in southernmost Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Hartmann, Leo A. [Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS (Brazil). Inst. de Geociencias; Liu, Dunyi; Wang, Yenbin [Chinese Academy of Geological Sciences, Beijing (China); Massonne, Hans-Joachim [Universitaet Stuttgart (Germany). Inst. fuer Mineralogie und Kristallchemie; Santos, Joao O.S. [University of Western Australia, Perth, WA (Australia). Centre for Global Targeting


    U-Pb dating of zircon was undertaken with the Beijing SHRIMP II (sensitive high resolution ion microprobe) on an amphibolite facies granodiorite and an almandine-albite granulite from the Santa Maria Chico Granulitic Complex, southern Brazilian Shield. This work was also done to unravel protolith ages which are often hidden in the array of partly reset data. The obtained metamorphic ages of the granodiorite gneiss and the granulite are 2035 {+-} 9 Ma and 2006 {+-} 3 Ma, respectively. These data are within the range of metamorphic ages determined in previous studies (2022 {+-} 18 Ma and 2031 {+-} 40 Ma). However, protolith ages for the granodiorite (2366 {+-} 8 Ma) and the granulite (2489 {+-} 6 Ma) were obtained which are outside the previously recognized range (> 2510-2555 Ma). The magmatic protolith age of the granodiorite refers to a previously little known magmatic event in the shield. Further investigations may demonstrate that amphibolite facies zircon crystals are useful as a window into geological events in associated granulites, because zircon ages are blurred in the studied granulites. (author)

  15. U-Th-Pb age in hydrothermal monazite applied in geochronological tin mineralization from Greisen zone of the Palanqueta granitic system, Bom Futuro deposit, Rondonia, Brazil; Datacao U-Th-Pb de monazita hidrotermal e sua aplicacao na geocronologia da mineralizacao de estanho em zonas de Greisen do sistema granitico Palanqueta, deposito do Bom Futuro, RO

    Energy Technology Data Exchange (ETDEWEB)

    Souza, Valmir da Silva [Universidade Federal do Amazonas, Manaus (Brazil). Inst. de Ciencias Exatas. Dept. de Geociencias]. E-mail:; Teixeira, Luciana Miyahara [Instituto Brasileiro do Meio Ambiente e dos Recursos Naturais Renovaveis (IBAMA), Brasilia, DF (Brazil)]. E-mail:; Botelho, Nilson Francisquini [Universidade de Brasilia, DF (Brazil). Inst. de Geociencias]. E-mail:


    The ages of hydrothermal events responsible for tin mineralization in the granitic systems from the Rondonia Tin Province are poorly defined so far. Available K-Ar dating in Li-micas of greisens and veins yielded values around 965 Ma, younger than the late mineralized granites ages, around 990 Ma. Electron microprobe U, Th and Pb dating of hydrothermal monazite from the greisen zones of the Palanqueta plutonic system, Bom Futuro tin deposit, yielded an age of 997{+-}48 Ma. Considering that: the K-Ar method is influenced by increasing temperature; critical temperature of Ar retention in micas is 300 deg C; and fluid inclusions and ae {sup 18}O studies indicate, respectively, trapping temperature above 300 deg C and cassiterite crystallization temperature above 400 deg C, we suggest that the K-Ar dating in micas from Rondonia tin deposits are indicative of cooling and closure of the hydrothermal systems. Therefore, ages obtained from U-Th-Pb data in hydrothermal monazite from greisen can be considered a good reference for the tin ore formation in the Bom Futuro deposit, associated with late to post-magmatic processes, and coeval with the end of crystallization of albite granite in the Palanqueta granitic system. (author)

  16. 浙江普陀山朱家尖產條絞長石的成因

    Institute of Scientific and Technical Information of China (English)



    @@ 一、引言 浙江省普陀山朱家尖產出的條絞長石,係何作霖先生1928年赴浙東調查時所採集者,其有關成分及結構等情况已詳見前中央研究院地質研究所叢刋第四號The Anorthoclase Perthite from Chu Chia Tsien Island near Putoshan,Cheking.文内.條絞長石生於花崗岩的氣穴裏,呈晶簇狀,晶體形狀如圖一所示,常常具有貝文歐雙晶(Baveno twin).薄片在顯微鏡下呈非常微細的條絞結構,與普通鉀鈉正長石(Anorthoclase)的構造相似,乃由於固溶體的分相作用所生成,惟在晶體内靠近邊緣的部分,往往有較厚的鈉長石(Albite)的薄片包裹在内,常平行(010)晶面,並且鈉長石與條絞長石的光性方位也完全一致,如圖二所示.

  17. Using presence of calcite cap rock in shales to predict occurrence of reservoirs composed of leached secondary porosity in the geopressured zone. Annual report, June 1, 1980-October 31, 1980

    Energy Technology Data Exchange (ETDEWEB)

    Kaiser, W.R.; Magara, K.; Milliken, K.L.; Richmann, D.L.


    The distribution of high-resistivity shale in the Frio Formation between hydropressured and geopressured strata has been mapped along the Texas Gulf Coast. Two high-resistivity intervals more than 1000 ft thick have been mapped, one in Brazoria and Galveston Counties and the other in Kenedy County. They coincide with Frio delta systems and may be related to extraordinary quantities of CO/sub 2/ produced by deltaic sediments rich in woody and herbaceous matter. Beyond being calcareous, the nature of the high-resistivity interval is enigmatic and its relationship to deep secondary porosity problematic. Most of the contained carbonate is microscopically and isotopically skeletal in origin, revealing no evidence of diagenetic modification. Minor rhombs of iron-bearing carbonate tens of microns in size were identified. Detrital feldspar compositions are being established to test subsequent changes in feldspar composition resulting from progressive burial and albitization. Hydrolysis reactions for authigenic minerals and reactions between key pairs of minerals have been written. Thermodynamic functions for complex phyllosilicates at temperatures up to 200/sup 0/C have been calculated. From thermodynamic calculations it was predicted that ferroan calcite would be the favored authigenic carbonate in shales.

  18. A survey of lunar rock types and comparison of the crusts of earth and moon (United States)

    Wood, J. A.


    The principal known types of lunar rocks are briefly reviewed, and their chemical relationships discussed. In the suite of low-KREEP highland rocks, Fe/(Fe + Mg) in the normative mafic minerals increases and the albite content of normative plagio-clase decreases as the total amount of normative plagioclase increases, the opposite of the trend predicted by the Bowen reaction principle. The distribution of compositions of rocks from terrestrial layered mafic intrusives is substantially different: here the analyses fall in several discrete clusters (anorthositic rocks, norites, granophyres and ferrogabbros, ultramafics), and the chemical trends noted above are not reproduced. It is suggested that the observed trends in lunar highland rocks could be produced by crystal fractionation in a deep global surface magma system if (1) plagiociase tended to float, upon crystallization, and (2) the magma was kept agitated and well mixed (probably by thermal convection) until crystallization was far advanced and relatively little residual liquid was left. After the crustal system solidified, but before extensive cooling had developed a thick, strong lithosphere, mantle convection was able to draw portions of the lunar anorthositic crust down into the mantle.

  19. Geology and Mineralogy of Uranium Deposits from Mount Isa, Australia: Implications for Albitite Uranium Deposit Models

    Directory of Open Access Journals (Sweden)

    Nick Wilson


    Full Text Available New geological, bulk chemical and mineralogical (QEMSCAN and FEG-EPMA data are presented for albitite-type uranium deposits of the Mount Isa region of Queensland, Australia. Early albitisation of interbedded metabasalt and metasiltstone predated intense deformation along D2 high strain (mylonite zones. The early sodic alteration paragenetic stage includes albite, riebeckite, aegirine, apatite, zircon and magnetite. This paragenetic stage was overprinted by potassic microveins, containing K-feldspar, biotite, coffinite, brannerite, rare uraninite, ilmenite and rutile. An unusual U-Zr phase has also been identified which exhibits continuous solid solution with a uranium silicate possibly coffinite or nenadkevite. Calcite, epidote and sulphide veinlets represent the latest stage of mineralisation. This transition from ductile deformation and sodic alteration to vein-controlled uranium is mirrored in other examples of the deposit type. The association of uranium with F-rich minerals and a suite of high field strength elements; phosphorous and zirconium is interpreted to be indicative of a magmatic rather than metamorphic or basinal fluid source. No large intrusions of appropriate age outcrop near the deposits; but we suggest a relationship with B- and Be-rich pegmatites and quartz-tourmaline veins.


    Institute of Scientific and Technical Information of China (English)

    程小苏; 陈倩


    Ceramic glazed tile was prepared by low temperature biscuit fire and high temperature glost fire using cinder from a ceramic factory' coal gasifier as the ceramic raw material. The phase composition and microstructure of ceramic glazed tile were analyzed by testing strength, water absorption, X-ray diffraction (XRD) and scanning electron microscopy (SEM). The effects of Albite and Black Talc to strength of ceramic body were discussed. When the content of cinder was 50%, the strength of ceramic tile was more than 35Mpa.%以煤气发生炉的煤渣为主要原料,辅以钠长石和黑滑石等其他原料,经低温素烧、高温釉烧的二次烧结工艺在辊道窑烧制成陶瓷釉面砖.测试其强度和吸水率,并采用X射线衍射(XRD)仪和扫描电子显微镜(SEM)分析了煤渣陶瓷釉面砖的物相组成及微观结构,探讨了配方中钠长石和黑滑石含量对陶瓷坯体强度的影响,制备出的陶瓷釉面砖强度大于35Mpa,且煤渣利用量可达50%.

  1. Regional, environmentally sound integrated protection of sorghum from the diseases in Samara Region

    Directory of Open Access Journals (Sweden)

    Evgenii Matvienko


    Full Text Available In the forest of the Samara region to major diseases of sorghum are striped bacterial blotch, Fusarium root rot and blight. Biological efficiency of chemical system products and Grands Prestige was 22-62 against root rots, bacteriosis 17-40% of bioproduct fitosporin-M and the growth regulator Albite respectively 6-32 and 4-21%. Against Alternaria effectiveness Prestige was 9-22%, fitosporin - 13-34%. By the phase of full ripeness when the intensity of bacteriosis 45-75% of plant height is reduced by 13, their weight - 11, the mass of grains per plant - 28, the number of grains per panicle - 20, the mass of 1000 seeds - 11%. Under the influence of pre-sowing seed treatment chemicals and Prestige Grands increased yield of grain sorghum grain at 4-12, sugar - by 5-9%. In experiments with irrigation at sowing in the average weather conditions for the years 2012-2013. biological grain yield increased in grain sorghum 13-20, sugar - by 28-32%. Important factors of stability of sorghum grain to the fungal infection of the genera Fusarium and Alternaria in the field include the presence on the seeds of the protective film. It may be noted that a significantly higher prevalence of grain grain sorghum, compared with diabetes, due to the fact that the seeds of grain sorghum naked and sweet sorghum filmy. This feature is important to consider in the selection of resistant varieties to this disease.

  2. Chemical evolution of acid precipitation in the unsaturated zone of the Pennsylvanian siltstones and shale of central Ohio (United States)

    Eckstein, Yoram; Lewis, Valerie E.; Bonta, James V.


    The North Appalachian Experimental Watershed in Coshocton, Ohio, USA has recorded average pH of precipitation of 4.7 over a 30-year period. The area lies within the Pennsylvanian siltstones and shale, dominated by aluminosilicates and lateral flow and seepage. The results from water-rock chemical reactions modeled using PHREEQM demonstrate the percolating precipitation water is neutralized to pH 7.5 within the top 1.5 m. The model suggests that, along with calcite, dissolution of albite, illite, and kaolinite are the dominant mechanisms of neutralization. The cation exchange capacity of the siltstone and shale, in the range 54.6-386 meq/100 g, appears to be a function of high organic carbon content of 2.0-3.2%. While cation exchange is responsible for some of the Na+ in solution, it is not the primary source of Ca2+, Mg2+, or K+ ions. Exchange onto clays is occurring, but is secondary to exchange on organic matter. Chemical composition of groundwater perched within a coal seam is controlled by oxidation and dissolution of pyrite, returning pH to approximately 4.0.

  3. Optimization of NaOH Molarity, LUSI Mud/Alkaline Activator, and Na2SiO3/NaOH Ratio to Produce Lightweight Aggregate-Based Geopolymer

    Directory of Open Access Journals (Sweden)

    Rafiza Abdul Razak


    Full Text Available This paper presents the mechanical function and characterization of an artificial lightweight geopolymer aggregate (ALGA using LUSI (Sidoarjo mud and alkaline activator as source materials. LUSI stands for LU-Lumpur and SI-Sidoarjo, meaning mud from Sidoarjo which erupted near the Banjarpanji-1 exploration well in Sidoarjo, East Java, Indonesia on 27 May 2006. The effect of NaOH molarity, LUSI mud/Alkaline activator (LM/AA ratio, and Na2SiO3/NaOH ratio to the ALGA are investigated at a sintering temperature of 950 °C. The results show that the optimum NaOH molarity found in this study is 12 M due to the highest strength (lowest AIV value of 15.79% with lower water absorption and specific gravity. The optimum LUSI mud/Alkaline activator (LM/AA ratio of 1.7 and the Na2SiO3/NaOH ratio of 0.4 gives the highest strength with AIV value of 15.42% with specific gravity of 1.10 g/cm3 and water absorption of 4.7%. The major synthesized crystalline phases were identified as sodalite, quartz and albite. Scanning Electron Microscope (SEM image showed more complete geopolymer matrix which contributes to highest strength of ALGA produced.

  4. Optimization of NaOH Molarity, LUSI Mud/Alkaline Activator, and Na2SiO3/NaOH Ratio to Produce Lightweight Aggregate-Based Geopolymer. (United States)

    Razak, Rafiza Abdul; Abdullah, Mohd Mustafa Al Bakri; Hussin, Kamarudin; Ismail, Khairul Nizar; Hardjito, Djwantoro; Yahya, Zarina


    This paper presents the mechanical function and characterization of an artificial lightweight geopolymer aggregate (ALGA) using LUSI (Sidoarjo mud) and alkaline activator as source materials. LUSI stands for LU-Lumpur and SI-Sidoarjo, meaning mud from Sidoarjo which erupted near the Banjarpanji-1 exploration well in Sidoarjo, East Java, Indonesia on 27 May 2006. The effect of NaOH molarity, LUSI mud/Alkaline activator (LM/AA) ratio, and Na2SiO3/NaOH ratio to the ALGA are investigated at a sintering temperature of 950 °C. The results show that the optimum NaOH molarity found in this study is 12 M due to the highest strength (lowest AIV value) of 15.79% with lower water absorption and specific gravity. The optimum LUSI mud/Alkaline activator (LM/AA) ratio of 1.7 and the Na2SiO3/NaOH ratio of 0.4 gives the highest strength with AIV value of 15.42% with specific gravity of 1.10 g/cm3 and water absorption of 4.7%. The major synthesized crystalline phases were identified as sodalite, quartz and albite. Scanning Electron Microscope (SEM) image showed more complete geopolymer matrix which contributes to highest strength of ALGA produced.

  5. Oxidative potential (OP) and mineralogy of iron ore particulate matter at the Gol-E-Gohar Mining and Industrial Facility (Iran). (United States)

    Soltani, Naghmeh; Keshavarzi, Behnam; Sorooshian, Armin; Moore, Farid; Dunster, Christina; Dominguez, Ana Oliete; Kelly, Frank J; Dhakal, Prakash; Ahmadi, Mohamad Reza; Asadi, Sina


    Concentrations of total suspended particulate matter, particulate matter with aerodynamic diameter ore PM. Accessory minerals are quartz, dolomite, hematite, actinolite, biotite, albite, nimite, laumontite, diopside, and muscovite. The scanning electron microscope structure of fibrous-elongated minerals revealed individual fibers in the range of 1.5 nm to 71.65 µm in length and 0.2 nm to 3.7 µm in diameter. The presence of minerals related to respiratory diseases, such as talc, crystalline silica, and needle-shaped minerals like amphibole asbestos (tremolite and actinolite), strongly suggests the need for detailed health-based studies in the region. The particulate samples show low to medium oxidative potential per unit of mass, in relation to an urban road side control, being more reactive with ascorbate than with glutathione or urate. However, the PM oxidative potential per volume of air is exceptionally high, confirming that the workers are exposed to a considerable oxidative environment. PM released by iron ore mining and processing activities should be considered a potential health risk to the mine workers and nearby employees, and strategies to combat the issue are suggested.

  6. A Petrographic and Mineralogical Study of Volcanic Rocks from the Mayaxueshan Area, North Qilian Fold Belt, NW China

    Institute of Scientific and Technical Information of China (English)

    徐达伟; 萧炎宏


    The Ordovician volcanic rocks in the Mayaxueshan area have been pervasively altered or metamorphosedand contain abundant secondary minerals such as albite, chlorite, epidote, prehnite, pumpellyite, actinolite, titanite, quartz,and/or calcite. They were denoted as spilites or spilitic rocks in terms of their petrographic features and mineral assem-blages. The metamorphic grades of the volcanic rocks are equivalent to that of the intercalated metaclastic rocks. Thisindicates that both the spilitic volcanic rocks and metaclastic rocks in the Mayaxueshan area have formed as a result ofCaledonian regional metamorphism. We suggest that the previously denoted spilitic rocks or altered volcanic rocks shouldbe re-denoted as metabasalts or metabasaltic rocks. The metamorphic grade of the volcanic rocks increases with their age:prehnite-pumpellyite facies for the upper part of the Middle Ordovician volcanic rocks, prehnite-pumpellyite to lowergreenschist facies for the lower part of the Middle Ordovician volcanic rocks, and lower greenschist facies for the LowerOrdovician volcanic rocks. The P-T conditions are estimated as T = 240 - 290C and P = 1.5 - 4.5 kbar for the lower partof the Middle Ordovician rocks, and T = ~ 300~C for the Lower Ordovician rocks. The variations of mineral assemblagesoccurring at different domains of the volcanic rocks were controlled by the variations of the effective bulk composition inthose domains during metamorphism. The geochemical characteristics of Mg-Al chromite in the Mayaxueshan volcanicrocks are consistent with an origin of island arc environment.

  7. Particle size and mineralogical composition of inorganic colloids in waters draining the adit of an abandoned mine, Goesdorf, Luxembourg

    Energy Technology Data Exchange (ETDEWEB)

    Filella, Montserrat [Department of Inorganic, Analytical and Applied Chemistry, University of Geneva, 30 quai Ernest-Ansermet, CH-1211 Geneva 4 (Switzerland); SCHEMA, Rue Principale 92, L-6990 Rameldange (Luxembourg)], E-mail:; Chanudet, Vincent [Department of Inorganic, Analytical and Applied Chemistry, University of Geneva, 30 quai Ernest-Ansermet, CH-1211 Geneva 4 (Switzerland); Institut F.-A. Forel, University of Geneva, 10 route de Suisse, CH-1290 Versoix (Switzerland); Philippo, Simon [Musee National d' Histoire Naturelle, 25 rue Muenster, L-2160 Luxembourg (Luxembourg); Quentel, Francois [Laboratoire de Chimie Analytique, UMR-CNRS 6521, Universite de Bretagne Occidentale, 6 avenue V. Le Gorgeu, F-29238 Brest Cedex 3 (France)


    Particle size distributions and the mineralogy of inorganic colloids in waters draining the adit of an abandoned mine (Goesdorf, Luxembourg) were quantified by single particle counting based on light scattering (100 nm-2 {mu}m) combined with transmission electronic microscopy coupled with energy dispersive spectroscopy and selected area electron diffraction. This water system was chosen as a surrogate for groundwaters. The dependence of the colloid number concentration on colloid diameters can be described by a power-law distribution in all cases. Power-law slopes ranged from -3.30 to -4.44, depending on water ionic strength and flow conditions. The same main mineral types were found in the different samples: 2:1 phyllosilicates (illite and mica), chlorite, feldspars (albite and orthoclase), calcite and quartz; with a variable number of Fe oxide particles. The colloid mineralogical composition closely resembles the composition of the parent rock. Spatial variations in the structure and composition of the rock in contact with the waters, i.e. fissured rock versus shear joints, are reflected in the colloid composition. The properties of the study colloids, as well as the processes influencing them, can be considered as representative of the colloids present in groundwaters.

  8. Petrogenesis of tourmaline rocks associated with Fe-carbonate graphite metapelite, metabasite and strata-bound polymetallic sulphide mineralisation, Peloritani Mountains, Sicily, Southern Italy (United States)

    Ferla, Paolo; Meli, Carmelina


    Tourmalinite and tourmaline-rich rocks associated with Fe-carbonate-graphite phyllite, strata-bound polymetallic sulphide deposits, metabasite and marble were studied, for information on the mechanism of tourmaline formation in the pre-Hercynian low-grade metamorphic sequence of the Mandanici Unit in the Peloritani Mountains of Sicily, southern Italy. The major and trace element compositions of the tourmaline rocks suggest the existence of a sedimentary protolith with pre-metamorphic black shale and bedded chert. Boron was interpreted to be accumulated in a restricted sedimentary basin, between platform carbonate formations, with abundant organic matter and Fe-Al-Ti-rich laterite-bauxite soil-derived clastic supply, under a continental volcano-tectonic extensional regime accompanied by a local convective hydrothermal system along faults. Petrographic, crystal-chemical and δ11B isotopic data are compatible with a model of marine sediment dewatering at temperatures below 200 °C, which caused the removal of boron from clay. Metamorphism led to the development of tourmaline in an Al-Ti-rich environment, in equilibrium with other minerals such as ilmenite, albite and muscovite. The upper temperature of metamorphism (almost 375 °C), estimated on the basis of δ11B, fits geothermometric results from Δ 13C carbonate-graphite on associated rocks. The estimated value of δ11B in the tourmalinite protolith, - 7.5‰ , is also compatible with continental-derived Al-rich sediments.

  9. 广东云开大山花岗岩类形成的初步实验研究

    Institute of Scientific and Technical Information of China (English)

    杨树锋; 蒋引珊


    This paper deals with the experimental studies on the formation of the reworkingtype(rpughly corresponding to S-typ)granites.All the experiments were based on extensive geological investigations into the Napeng granite body of Luoding,Guangdong Province.Thie granite body was formed by reworking and metasomatism of metamorphie rocks which had reached the amphibolite facies,For this reason,the metamorphic rocks consisting mainly of quartz-ica-schists were taken as the starting materials in the experiments.At 1kb and 400°-550℃ the samples of quartz-mica schist reacted with various Na-and K-rich aqueous solutions,resulting in the quartz-albite-biotite and quartz-K-feldspar-biotite assemblages similar to those in the granites.In addition,several initial melting and melting-erystallization experiments on metamorphic rocks and migmatites were performed at 1-2kb and 550°-990℃,Moreover,the equilibrium constants for the reactions were computed at 400°-600℃ ad 1-2kb on the basis of J.D.Frantz's data on the solubility of minerals.Experimental data and thermodynamic calculations indicate that the reworkingtype granites were formed from metamorphic rocks,such as quartz-schist,through reaction with alkali-silicate aquous solutions.

  10. Moessbauer spectroscopy and X-ray diffraction analyses of clayey samples used as ceramic sourcing materials, in Peru

    Energy Technology Data Exchange (ETDEWEB)

    Quille, Ruben, E-mail:; Bustamante, Angel [San Marcos National University, Laboratory of Ceramics and Nanomaterials, Faculty of Physical Sciences (Peru); Palomino, Ybar [National University of San Cristobal de Huamanga, Experimental Center of Ceramics (Peru)


    The ceramic industry is an important area of economic activity in the Ayacucho Region, in particular in the District of Quinua. As a consequence, there is a huge demand for clay to produce ceramic pastes in that region. This paper reports on results concerning the mineralogical characterization of four clayey samples, which were collected MAA and SPQA from the area Pampa de La Quinua with geographic coordinates 13 Degree-Sign 02 Prime 49 Double-Prime S 74 Degree-Sign 08 Prime 03 Double-Prime W, CE1M and CE2M from the Quinua locality 13 Degree-Sign 03 Prime 07 Double-Prime S 74 Degree-Sign 08 Prime 31 Double-Prime W, both in the District of Quinua, Province of Huamanga, Ayacucho, Peru. The chemical and mineralogical characterization of these samples was carried out with powder X-ray diffraction detecting quartz, albite, montmorillonite, kaolinite and glauconite mineral phases, Moessbauer spectroscopy detected iron in kaolinite, glauconite and montmorillonite minerals. Chemical analysis was performed through scanning electron microscopy and energy dispersive X-ray spectroscopy. Data obtained from the combination of these techniques provided relevant information about the morphology, chemical composition, and the mineralogy of samples.

  11. Mössbauer spectroscopy and X-ray diffraction analyses of clayey samples used as ceramic sourcing materials, in Peru (United States)

    Quille, Rubén; Bustamante, Ángel; Palomino, Ybar


    The ceramic industry is an important area of economic activity in the Ayacucho Region, in particular in the District of Quinua. As a consequence, there is a huge demand for clay to produce ceramic pastes in that region. This paper reports on results concerning the mineralogical characterization of four clayey samples, which were collected MAA and SPQA from the area Pampa de La Quinua with geographic coordinates 13° 02' 49″ S 74° 08' 03″ W, CE1M and CE2M from the Quinua locality 13° 03' 07″ S 74° 08' 31″ W, both in the District of Quinua, Province of Huamanga, Ayacucho, Peru. The chemical and mineralogical characterization of these samples was carried out with powder X-ray diffraction detecting quartz, albite, montmorillonite, kaolinite and glauconite mineral phases, Mössbauer spectroscopy detected iron in kaolinite, glauconite and montmorillonite minerals. Chemical analysis was performed through scanning electron microscopy and energy dispersive X-ray spectroscopy. Data obtained from the combination of these techniques provided relevant information about the morphology, chemical composition, and the mineralogy of samples.

  12. Crystal chemical control of clinopyroxene-melt partitioning in the Di-Ab-An system: implications for elemental fractionations in the depleted mantle

    Energy Technology Data Exchange (ETDEWEB)

    Lundstrom, C. C.; Shaw, H. F.; Ryerson, F. J.; Williams, Q.; Gill, J.


    The partitioning of fifteen trace elements (Rb, Sr, Zr, Nb, Ba, La, Ce, Nd, Sm, Gd, Yb, Hf, Ta, Pb and Th) between clinopyroxene and synthetic melt has been studied in two compositions along an isotherm in the diopside-albite-anorthite ternary at 1 bar pressure. The two compositions correspond to ~ Di65An35 and ~ Di55Ab45 and produce clinopyroxenes distinct in chemistry while melt compositions range from 49 wt % SiO2 to 61 wt. % SiO2. The partition coefficients of high field strength elements (HFSE) increase by factors of 2 to 8 in Di-An experiments relative to Di-Ab experiments while other elements show very little change (+/- 20%) between compositions. The change in HFSE partitioning correlates with increases in tetrahedral Al2O3 (IVAl) content of clinopyroxenes in the anorthite-bearing experiments. Changes in DTa/DNb also correlate with IVA1 based on a survey of previously published determinations.

  13. Use of basaltic waste as red ceramic raw material

    Directory of Open Access Journals (Sweden)

    T. M. Mendes

    Full Text Available Abstract Nowadays, environmental codes restrict the emission of particulate matters, which result in these residues being collected by plant filters. This basaltic waste came from construction aggregate plants located in the Metropolitan Region of Londrina (State of Paraná, Brazil. Initially, the basaltic waste was submitted to sieving (< 75 μm and the powder obtained was characterized in terms of density and particle size distribution. The plasticity of ceramic mass containing 0%, 10%, 20%, 30%, 40% and 50% of basaltic waste was measured by Atterberg method. The chemical composition of ceramic formulations containing 0% and 20% of basaltic waste was determined by X-ray fluorescence. The prismatic samples were molded by extrusion and fired at 850 °C. The specimens were also tested to determine density, water absorption, drying and firing shrinkages, flexural strength, and Young's modulus. Microstructure evaluation was conducted by scanning electron microscopy, X-ray diffraction, and mercury intrusion porosimetry. Basaltic powder has similar physical and chemical characteristics when compared to other raw materials, and contributes to ceramic processing by reducing drying and firing shrinkage. Mechanical performance of mixtures containing basaltic powder is equivalent to mixtures without waste. Microstructural aspects such as pore size distribution were modified by basaltic powder; albite phase related to basaltic powder was identified by X-ray diffraction.

  14. Assessment of geochemical evolution of groundwater in a mountainous area under agricultural land (United States)

    Ledesma-Ruiz, Rogelio; Pasten-Zapata, Ernesto; Parra, Roberto; Harter, Thomas; Mahlknecht, Jürgen


    Zona Citricola is an important area to Mexico for its citriculture. Situated in a sub-humid to humid climate adjacent to Sierra Madre Occidental, this mountainouos valley hosts an aquifer system which represents sequences of shales, marls, conglomerates, and alluvial deposits. Groundwater flows from mountainous recharge areas to the basin-fill deposits and provides base flow to supply drinking water to an adjacent metropolitan area. The objective of this study was to characterize groundwater chemistry of this area and to assess the evolution. Correlation and principal component analysis were used to decipher various underlying natural and anthropogenic processes creating distinct water classes: (1) dissolution of evaporates, (2) surface organic waste or wastewater, and (3) silicate weathering and clay formation. Hierarchical cluster analysis was employed for partitioning the water samples into four hydrochemical groups: recharge waters (Ca-HCO3), transition zone waters (Ca-HCO3-SO4 to Ca-SO4-HCO3) and discharge waters (Ca-SO4). Inverse geochemical models of these groups were developed using PHREEQC to elucidate the chemical reactions controlling water chemistry between an initial (recharge) and final water. The main responsible reactions were: (1) dissolution of rock salts, (2) release of soil gas carbon dioxide, (3) dedolomitization,(4) albite weathering reactions with corresponding precipitation of silica and clay minerals, and (5) input from animal/human waste and manure, accompanied by denitrification processes. The hydrochemical groups could be related to lithological formations.

  15. Inherited igneous zircons in jadeitite predate high-pressure metamorphism and jadeitite formation in the Jagua Clara serpentinite mélange of the Rio San Juan Complex (Dominican Republic) (United States)

    Hertwig, Andreas; McClelland, William C.; Kitajima, Kouki; Schertl, Hans-Peter; Maresch, Walter V.; Stanek, Klaus; Valley, John W.; Sergeev, Sergey A.


    This study utilizes zircon SIMS U-Pb dating, REE and trace-element analysis as well as oxygen isotope ratios of zircon to distinguish jadeite-rich rocks that formed by direct crystallization from a hydrous fluid from those that represent products of a metasomatic replacement process. Zircon was separated from a concordant jadeitite layer and its blueschist host, as well as from loose blocks of albite-jadeite rock and jadeitite that were all collected from the Jagua Clara serpentinite-matrix mélange in the northern Dominican Republic. In the concordant jadeitite layer, three groups of zircon domains were distinguished based on both age as well as geochemical and oxygen isotope values: age groups old (117.1 ± 0.9 Ma), intermediate (three dates: 90.6, 97.3, 106.0 Ma) and young (77.6 ± 1.3 Ma). Zircon populations from the blueschist host as well as the other three jadeite-rich samples generally match zircon domains of the old age group in age as well as geochemistry and oxygen isotope ratios. Moreover, these older zircon populations are indistinguishable from zircon typical of igneous oceanic crust and hence are probably inherited from igneous protoliths of the jadeite-rich rocks. Therefore, the results suggest that all investigated jadeite-rich rocks were formed by a metasomatic replacement process. The younger domains might signal actual ages of jadeitite formation, but there is no unequivocal proof for coeval zircon-jadeite growth.

  16. Compositional controls on spinel clouding and garnet formation in plagioclase of olivine metagabbros, Adirondack Mountains, New York (United States)

    McLelland, J.M.; Whitney, P.R.


    Olivine metagabbros from the Adirondacks usually contain both clear and spinel-clouded plagioclase, as well as garnet. The latter occurs primarily as the outer rim of coronas surrounding olivine and pyroxene, and less commonly as lamellae or isolated grains within plagioclase. The formation of garnet and metamorphic spinel is dependent upon the anorthite content of the plagioclase. Plagioclase more sodic than An38??2 does not exhibit spinel clouding, and garnet rarely occurs in contact with plagioclase more albitic than An36??4. As a result of these compositional controls, the distribution of spinel and garnet mimics and visually enhances original igneous zoning in plagioclase. Most features of the arrangement of clear (unclouded) plagioclase, including the shells or moats of clear plagioclase which frequently occur inside the garnet rims of coronas, can be explained on the basis of igneous zoning. The form and distribution of the clear zones may also be affected by the metamorphic reactions which have produced the coronas, and by redistribution of plagioclase in response to local volume changes during metamorphism. ?? 1980 Springer-Verlag.

  17. Sludge granulation and efficiency of phase separator in UASB reactor treating combined industrial effluent

    Institute of Scientific and Technical Information of China (English)

    Abdullah Yasar; Nasir Ahmad; Muhammad Nawaz Chaudhry; Aamir Amanat Ali Khan


    Sludge granulation and the effect of gas-liquid-solid separator (GLSS) design on the efficiency of upflow anaerobic sludge blanket (UASB) and upflow anaerobic sludge filter (UASF) reactors, operating at HRTs ranging from 3 to 12 h was investigated. VSS/TS ratio gradually increased in both the reactors with increasing sludge age (from 0.5 to more than 0.7 for UASB reactor and 0.012 to 0.043 for UASF reactor). X-Ray diffraction analysis of the UASF sludge showed the presence of expanding clays revealing its additional absorption capability. Fuoraphyllite and albite precipitation related to excellular polymers of the microbial shell structure, showed the extended growth of microorganisms during sludge granulation. A gradual decrease (82%-69%) in COD removal with decreasing HRT was apparent in UASF reactor. In case of UASB reactor, this decrease was marginal because addition of GLSS device significantly improved (14%-20%) the overall efficiency of the UASB reactor. GLSS enhanced the efficiency of the UASB reactor by increasing the settleability of suspended particles and accelerating the coagulation of colloidal particles due to the velocity gradient.

  18. Adakite-type sodium-rich rocks in Awulale Mountain of west Tianshan: Significance for the vertical growth of continental crust

    Institute of Scientific and Technical Information of China (English)


    The sodium-rich dacites and albite porphyries of Permian in the Awulale Mountain of west Tianshan have unique chemical and trace element signatures identical to adakite. These intermediate-acidic igneous rocks are characterized by high Na2O, Al2O3 and Sr contents and high Sr/Y and La/Y ratios (>40 and >20, respectively), and low Y and Yb contents, and strong depletion in HREE, and posi- tive Eu anomaly. The (143Nd/144Nd)i is in the range from 0.51236 to 0.51248 and the e Nd(t) is positive value (+0.79- +3.11); the (87Sr/86Sr)i is in the range from 0.7052 to 0.7054. These Nd and Sr isotopic composition features indicate that the source rocks of these adakite-type rocks are from a weakly depleted mantle, or a depleted mantle, but was con-taminated by the crustal materials. These adakite-type rocks were most likely derived from the partial melting of new underplated basaltic rocks under the conditions of amphibo-lite to eclogite transition in the postcollisional environment of North Xinjiang during the Permian Period. They are not only the Phanerozoic juvenile crust materials, but also are probably animportant symbol of the underplating of mantle- derived basaltic magmas and the vertical growth of continen-tal crust in the west Tianshan area during the postcollision of Late Paleozoic.

  19. Geochemistry of Rare Earth Elements (REE) in the Weathered Crusts from the Granitic Rocks in Sulawesi Island, Indonesia

    Institute of Scientific and Technical Information of China (English)

    Adi Maulana; Kotaro Yonezu; Koichiro Watanabe


    We report for the first time the geochemistry of rare earth elements (REE) in the weath-ered crusts of I-type and calc-alkaline to high-K (shoshonitic) granitic rocks at Mamasa and Palu re-gion, Sulawesi Island, Indonesia. The weathered crusts can be divided into horizon A (lateritic profile) and B (weathered horizon). Quartz, albite, kaolinite, halloysite and montmorrilonite prevail in the weathered crust. Both weathered profiles show that the total REE increased from the parent rocks to the horizon B but significantly decrease toward the upper part (horizon A). LREE are enriched toward the upper part of the profile as shown by La/YbN value. However, HREE concentrations are high in horizon B1 in Palu profile. The total REE content of the weathered crust are relatively elevated com-pared to the parent rocks, particularly in the lower part of horizon B in Mamasa profile and in horizon B2 in Palu profile. This suggests that REE-bearing accessory minerals may be resistant against weath-ering and may remain as residual phase in the weathered crusts. The normalized isocon diagram shows that the mass balance of major and REE components between each horizon in Mamasa and Palu weathering profile are different. The positive Ce anomaly in the horizon A of Mamasa profile indicated that Ce is rapidly precipitated during weathering and retain at the upper soil horizon.

  20. Metallogenetic modeling for uranium exploration in rocks of the Abaira-Jussiape Anticlinal nucleus, Chapada Diamantina, Bahia; Modelagem metalogenetica para prospeccao de uranio nas rochas do nucleo da Anticlinal Abaira-Jussiape, Chapada Diamantina, Bahia

    Energy Technology Data Exchange (ETDEWEB)

    Santana, Jocilene dos Santos; Cruz, Simone Cerqueira Pereira; Barbosa, Johildo Salomao Figueiredo [Universidade Federal da Bahia (PPGG/UFBA), Salvador, BA (Brazil); Abram, Maisa Bastos; Martins, Adriano Alberto Marques, E-mail:, E-mail:, E-mail:, E-mail:, E-mail: [Companhia de Pesquisas de Recursos Minerais (CPRM), Salvador, BA (Brazil). Superintendencia Regional de Salvador. Servico Geologico do Brasil


    The NNW-SSE-trending Abaira-Jussiape Anticlinal is an antiformal culmination of folding and shearing in the Paramirim Corridor of the Western Chapada Diamantina. In its core paleoproterozoic, mylonitized Caraguatai Suite, tonalites-granodiorites, alkali-feldspar granites, syenites to quartz-syenites and Jussiape Suite granites crop out. Compressional and distensional stresses mark the structural geology of the area. The compressional structures are related to two distinct deformation phases, named D1a and D1b. The main compressional phase is ductile D1a, which is related to the nucleation of dextral to dextral-reverse shearing zones. Deformation and syn-D1a recrystallization involving plagioclase and the K-feldspar suggest deformation temperature conditions above 550 deg C. The following phase D2 is of ductilebrittle nature and culminates in reverse shearing zones. The distensional structures correspond to the D3 phase and are represented by frontal shear zones with normal movement. The petrographic study helped identify a pre-D1a hydrothermal alteration process related to albitization and potassification, syn-D1 oxidation process, and hydration and saussuritization related to phases D2 and D3. The integration of lithological, petrographic, structural and geophysical data by means of the logic Fuzzy, plus the existing information regarding structural and lithologic controls of the known uranium mineralization in the Paramirim Corridor, led us to identify two promising areas for radioactive element exploration in the nucleus of Abaira-Jussiape Anticlinal. (author)

  1. Properties of ceramics prepared using dry discharged waste to energy bottom ash dust. (United States)

    Bourtsalas, Athanasios; Vandeperre, Luc; Grimes, Sue; Themelis, Nicolas; Koralewska, Ralf; Cheeseman, Chris


    The fine dust of incinerator bottom ash generated from dry discharge systems can be transformed into an inert material suitable for the production of hard, dense ceramics. Processing involves the addition of glass, ball milling and calcining to remove volatile components from the incinerator bottom ash. This transforms the major crystalline phases present in fine incinerator bottom ash dust from quartz (SiO(2)), calcite (CaCO(3)), gehlenite (Ca(2)Al(2)SiO(7)) and hematite (Fe(2)O(3)), to the pyroxene group minerals diopside (CaMgSi(2)O(6)), clinoenstatite (MgSi(2)O(6)), wollastonite (CaSiO(3)) together with some albite (NaAlSi(3)O(8)) and andradite (Ca(3)Fe(2)Si(3)O(12)). Processed powders show minimal leaching and can be pressed and sintered to form dense (>2.5 g cm(-3)), hard ceramics that exhibit low firing shrinkage (ceramic tiles that have potential for use in a range of industrial applications.

  2. Analysis of deterioration of rocky material which conform the sculptured serpents of the Tenayuca pyramid; Analisis del deterioro del material petreo que conforman las serpientes esculpidas de la piramide de Tenayuca

    Energy Technology Data Exchange (ETDEWEB)

    Mendoza A, D. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico); Martinez C, G. [INAH, 04000 Coyoacan (Mexico); Rodriguez L, V. [BUAP, A.P. J-48, 72520 Puebla (Mexico)


    This work presents the results about the characterization of rocky materials samples proceeding from heads of snakes that adorn the pyramid of Tenayuca, Mexico. Analysis of these samples, that show deterioration presence was performance through Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDS) and X-ray Diffraction (XRD). Several morphological structures such as granular, tubular, acicular growths and fibers were observed, some of they could be associate to salt migration. It was possible to identify different crystalline phases associated with albite (NaAlSi{sub 3}O{sub 8}), anorthite [(Ca,Na)(Si,Al){sub 4}O{sub 8}], ferroactinolite [(Ca,Na,K){sub 2} Fe{sub 5}Si{sub 8}O{sub 22}(OH){sub 2}], gypsum (CaSO{sub 4} 2H{sub 2}O), quartz (SiO{sub 2}) and thenardite (Na{sub 2}SO{sub 4}). (Author) 10 refs., 2 tabs., 12 figs.

  3. Salinity variations and chemical compositions of waters in the Frio Formation, Texas Gulf Coast. Annual report

    Energy Technology Data Exchange (ETDEWEB)

    Morton, R.A.; Garrett, C.M. Jr.; Posey, J.S.; Han, J.H.; Jirik, L.A.


    Waters produced from sandstone reservoirs of the deep Frio Formation exhibit spatial variations in chemical composition that roughly coincide with the major tectonic elements (Houston and Rio Grande Embayments, San Marcos Arch) and corresponding depositional systems (Houston and Norias deltas, Greta-Carancahua barrier/strandplain system) that were respectively active along the upper, lower, and middle Texas Coast during Frio deposition. Within an area, salinities are usually depth dependent, and primary trends closely correspond to pore pressure gradients and thermal gradients. Where data are available (mainly in Brazoria County) the increases in TDS and calcium with depth coincide with the zone of albitization, smectite-illite transition, and calcite decrease in shales. Waters have fairly uniform salinities when produced from the same sandstone reservoir within a fault block or adjacent fault blocks with minor displacement. In contrast, stratigraphically equivalent sandstones separated by faults with large displacement usually yield waters with substantially different salinities owing to the markedly different thermal and pressure gradients across the faults that act as barriers to fluid movement.

  4. Thermoluminescent characteristics of oregano and paprika

    Energy Technology Data Exchange (ETDEWEB)

    Cruz Z, E.; Furetta, C.; Teuffer Z, C. [ICN-UNAM, A.P. 70-543, 04510 Mexico D.F. (Mexico); Melendrez, R.; Barboza F, M. [Universidad de Sonora, A.P. 5-88, Hermosillo, Sonora (Mexico); Kitis, G. [Nuclear Physics Laboratory, Aristotle University of Thessaloniki, 54006 Thessaloniki (Greece)


    The poly minerals from oregano and paprika were selected according to different sizes, i.e 10, 53, 74, 149 {mu}m, and they were exposed to ionizing gamma radiation in the range of doses 0.5-45 kGy. The glow curves from these spices show an abroad TL band, centered around 150 C and by XRD analysis shows a mono mineral composition mainly quartz and feldspar, including albite, ortose and clay. The fading behavior was related to the quartz, feldspar and calcite TL properties and shown the stability of the traps associated to the defects generated by irradiation in the samples. The tendency of the TL integrated was increased with the grain size for oregano and can be related to the different energy values associated to the activation energy of the traps in the monominerals. The glow curve TL from poly minerals was analyzed and it is possible to use the dosimetric property of the poly minerals from spices for detect irradiated foodstuffs. (Author)

  5. The structure and petrography of alkaline rocks of the Mada Younger Granite complex, Nigeria (United States)

    Abaa, S. I.

    The structural aspects of the Mada Younger Granite complex differ from those described from other ring complexes in the province. Ring-dykes and cauldron subsidence structures are not observed and the extrusive rhyolites do not appear to be related to a volcanic cauldron. The minor remnants of the extrusive rocks were domes over small vents since there are no clear indications of any unified volcanic structure. Volcanic eruptions may have taken place from dispersed vents probably including pipes and fissures. Linear intrusive structures have been observed and there is no concentric arrangement of rock units. The biotite granites appear more as sheet structures dipping gently to the south. Petrographically, the extrusive rocks are rhyolites, the comenditic ignimbrite being distinctly peralkaline with aegirine and arfvedsonite. The granite cupolas may be classified as 'A'-type and have been affected by pervasive potash metasomatism which caused recrystallization with microline and finely twinned clear euhedral albite, together with mica compositions between annite towards lithian siderophyllite. This process also introduced minerals like fluorite, cassiterite, columbite and thorite which make the Mada complex a possible source for economic minerals.

  6. Fluid geochemistry of the Acqui Terme-Visone geothermal area (Piemonte, Italy)

    Energy Technology Data Exchange (ETDEWEB)

    Marini, L.; Bonaria, V.; Ottonello, G.; Zuccolini, M.V. [University of Genova (Italy). Dip. per lo Studio del Territorio e delle sur Risorse; Guidi, M. [Istituto di Geocronologia e Geochimica Isotopica, CNR, Pisa (Italy); Hunziker, J.C. [Universite de Lausanne (Switzerland). Inst. de Mineralogie et Petrographie


    The main geothermal reservoir of Acqui Terme-Visone hosts Na-Cl waters, which are in chemical equilibrium at 120-130{sup o}C with typical hydrothermal minerals including quartz, albite, K-feldspar, illite. chlorite (or smectite), anhydrite, calcite and an unspecified Ca-Al-silicate. In the Acqui Terme-Visone area, these geothermal waters ascend along zones of high vertical permeability and discharge at the surface almost undiluted or mixed with cold, shallow waters. To the SW of Acqui Terme, other ascending geothermal waters, either undiluted or mixed with low-salinity waters, enter relatively shallow secondary reservoirs, where they reequilibrate at 65-70{sup o}C. Both chemical and isotopic data indicate that bacterial SO{sub 4} reduction affects all these waters, especially those discharged by the secondary reservoirs. Therefore, geothermal waters must get in contact with oil, acquiring the relatively oxidized organic substances needed by SO{sub 4} -reducing bacteria. This oil-water interaction process deserves further investigations, for potential economic implications. (Author)

  7. Quantitative analysis of H-species in anisotropic minerals by polarized infrared spectroscopy along three orthogonal directions (United States)

    Shuai, Kang; Yang, Xiaozhi


    Infrared spectroscopy is a powerful technique for probing H-species in nominally anhydrous minerals, and a particular goal of considerable efforts has been providing a simple yet accurate method for the quantification. The available methods, with either polarized or unpolarized analyses, are usually time-consuming or, in some cases, subjected to larger uncertainty than theoretically expected. It is shown here that an empirical approach for measuring the concentration, by determining three polarized infrared spectra along any three mutually perpendicular directions, is theoretically and in particular experimentally correct. The theoretical background is established by considering the integrated absorbance, and the experimental measurements are based on a careful evaluation of the species and content of H in a series of gem-quality orthogonal, monoclinic and triclinic crystals, including olivine, orthopyroxene, clinopyroxene, orthoclase and albite (natural and H-annealed). The results demonstrate that the sum of the integrated absorbance from two polarized spectra along two perpendicular directions in any given plane is a constant, and that the sum of the integrated absorbance from three polarized spectra along any three orthogonal directions is of essentially the same accuracy as that along the principal axes. It is also shown that this method works well, with a relative accuracy within 10%, even at some extreme cases where the sample absorption bands are both intense and strongly anisotropic.

  8. An unusual radiation dose dependent EPR line at g{sub eff} = 2.54 in feldspars: possible evidence of Fe{sup 3+}O{sup 2-} {r_reversible} Fe{sup 2+}O{sup -} and exchange coupled Fe{sup 3+}-Fe{sup 2+}-nO{sup -}

    Energy Technology Data Exchange (ETDEWEB)

    Sastry, M D [Physical Research Laboratory, Navrangpura, Ahmedabad, 380 009 (India); Nagar, Y C [Physical Research Laboratory, Navrangpura, Ahmedabad, 380 009 (India); Bhushan, B [Food Technology Division, Bhabha Atomic Research Center, Trombay, Mumbai, 400 085 (India); Mishra, K P [Radiation Biology and Health Sciences, Bhabha Atomic Research Center, Mumbai, 400 085 (India); Balaram, V [Geochemistry Division, National Geophysical Research Institute, Hyderabad, 500 007 (India); Singhvi, A K [Physical Research Laboratory, Navrangpura, Ahmedabad, 380 009 (India)


    We report electron paramagnetic resonance (EPR) results on natural feldspar grains extracted from sediment samples of three widely different source regions. The XRD analysis indicated that the samples had albite, microcline and Ca/Ba-orthoclase as the major constituents. The EPR spectrum of all the samples exhibited an intense line around g{sub eff} = 4.3. This is characteristic of Fe{sup 3+} with a zero field splitting that is significantly larger than the microwave quantum. More interesting was the presence of a strong EPR signal in the region of g{sub eff} = 2.54-2.7. On irradiation with gamma rays the position of the line shifted to higher magnetic field. The possible origin of this line and its unusual behavior with dose is explained as being due to the interaction of a hopping 'hole' on oxygen with iron centers. The possibilities considered include (1) the valence fluctuation of an Fe{sup 3+} center at a tetrahedral site (2) oscillation of FeO{sub 4}{sup -} between two resonant forms, Fe{sup 2+}O{sup -} and Fe{sup 3+}O{sup 2-}, and (3) exchange coupling between Fe{sup 3+}, Fe{sup 2+} and O{sup -}. The concentration of the latter is dose dependent and, consequently, it results in the observed dose dependent line shift.

  9. Formation of cordierite-bearing lavas during anatexis in the lower crust beneath Lipari Island (Aeolian arc, Italy) (United States)

    di Martino, Corrado; Forni, Francesca; Frezzotti, Maria Luce; Palmeri, Rosaria; Webster, James D.; Ayuso, Robert A.; Lucchi, Federico; Tranne, Claudio A.


    Cordierite-bearing lavas (CBL;~105 ka) erupted from the Mt. S. Angelo volcano at Lipari (Aeolian arc, Italy) are high-K andesites, displaying a range in the geochemical and isotopic compositions that reflect heterogeneity in the source and/or processes. CBL consist of megacrysts of Ca-plagioclase and clinopyroxene, euhedral crystals of cordierite and garnet, microphenocrysts of orthopyroxene and plagioclase, set in a heterogeneous rhyodacitic-rhyolitic groundmass containing abundant metamorphic and gabbroic xenoliths. New petrographic, chemical and isotopic data indicate formation of CBL by mixing of basaltic-andesitic magmas and high-K peraluminous rhyolitic magmas of anatectic origin and characterize partial melting processes in the lower continental crust of Lipari. Crustal anatectic melts generated through two main dehydration-melting peritectic reactions of metasedimentary rocks: (1) Biotite + Aluminosilicate + Quartz + Albite = Garnet + Cordierite + K-feldspar + Melt; (2) Biotite + Garnet + Quartz = Orthopyroxene + Cordierite + K-feldspar + Melt. Their position into the petrogenetic grid suggests that heating and consequent melting of metasedimentary rocks occurred at temperatures of 725 Lipari was induced by protracted emplacement of basic magmas in the lower crust (~130 Ky). Crustal melting of the lower crust at 105 ka affected the volcano evolution, impeding frequent mafic-magma eruptions, and promoting magma stagnation and fractional crystallization processes.

  10. Origin of the glauconite from the Middle Eocene, Qarara Formation, Egypt (United States)

    Hegab, Omar A.; Abd El-Wahed, Ahmed G.


    Although the Middle Eocene sediments at the Nile Valley, Egypt have been extensively studied, the origin of glauconites in these sediments is still questionable. In this paper, the glauconites that occur in the Qarara Formation were subjected to petrographical and mineralogical studies to assess their origin. Glauconite pellets or grains have been separated from the glauconitic sandy units of the studied three sections. They are present in different colors and different forms. X-ray diffraction analysis indicated that bulk samples are composed of mixed - layer clays (illite-montmorillonite), quartz, microcline, and albite. The separated glauconite grains are present in two shapes, the first is spherical and the second is elliptical, both are green in color with different grades. They are authigenic in origin as evidenced by high sorting, presence of deep or surficial fractures, and as supported to form by alteration of fecal pellets. They are also less mature as evidenced by their pale green color and by the higher expandable layer contents in their mixed-layer clay composition.

  11. A Preliminary Study on the Evolutionary Characteristics of Rare Earth Elements (REE)in Granitoid Rocks and Their Formation Mechanisms in Xianghualing Region,Hunan Province,China

    Institute of Scientific and Technical Information of China (English)

    杜绍华; 邱瑞照


    Recognized in the Xianghualing region,South Hunan are three major types of granitoids,i.e.,biotite granite,zinnwaldite-albite granite and xianghuagite,which evolved form the same granitic magma,but were formed at different stages.These granitoid rocks constitute a complete magmatic evolutionary series.With the evolution of magma,REE contents and negative Eu anomalies tend to decrease progressively,and LREE become more and more enriched relative to HREE .The facts mentioned above show that the tendency of REE evolution in granitoid rocks in the region studied is different from that in other regions.Evidence indicates that the granitic magma system became more and more depleted in Si(K+Na),but richer and richer in Al,Li,F and H2O+ during the process of its evolution,re-sulting in relatively weak acidity and strong alkalinity .It may be the most important factor leading to a specific REE evolutionary trend for the granitoid rocks in this region.In addition,the changing oxidation-reduction environments at different evolutionary stages of this magma system may be anoth-er important factor which should be taken into consideration.

  12. Protolith age of Santa Maria Chico granulites dated on zircons from an associated amphibolite-facies granodiorite in southernmost Brazil. (United States)

    Hartmann, Léo A; Liu, Dunyi; Wang, Yenbin; Massonne, Hans-Joachim; Santos, João O S


    U-Pb dating of zircon was undertaken with the Beijing SHRIMP II (sensitive high resolution ion microprobe) on anamphibolite facies granodiorite and an almandine-albite granulite from the Santa Maria Chico Granulitic Complex, southern Brazilian Shield. This work was also done to unravel protolith ages which are often hidden in the array of partly reset data. The obtained metamorphic ages of the granodiorite gneiss and the granulite are 2035 +/- 9 Ma and 2006 +/- 3 Ma, respectively. These data are within the range of metamorphic ages determined in previous studies (2022 +/- 18 Ma and 2031 +/- 40 Ma). However, protolith ages for the granodiorite (2366 +/- 8 Ma) and the granulite (2489 +/- 6 Ma) were obtained which are outside the previously recognized range (> 2510-2555 Ma). The magmatic protolith age of the granodiorite refers to a previously little known magmatic event in the shield. Further investigations may demonstrate that amphibolite facies zircon crystals are useful as a window into geological events in associated granulites, because zircon ages are blurred in the studied granulites.

  13. Biogenic characteristics of Mesozoic cherts in southern Tibet and its significance

    Institute of Scientific and Technical Information of China (English)

    何俊国; 周永章; 李红中


    The Xialu chert, which contains abundant biological information, were investigated by major element analysis, micro-Raman, SEM and EPMA. The results show that SiO2 content of chert is 84.12%-93.08%, averaging 89.84%. The close packed structures of low degree crystallinity of quartz indicate the hydrothermal origin. SiO2 of modern hot springs exhibit loose silica pellets and nodular, beaded structures. Under polarization microscope, the presence of biological skeleton structures indicate that biological activities are involved in the hydrothermal deposition, which correspond to the geochemical characteristics:w(SiO2)/w(K2O+Na2O), w(SiO2)/w(Al2O3) and w(SiO2)/w(MgO), with average values of 295.29, 68.88 and 284.45, respectively. SiO2 is enriched in the organism (radiolarian) centers, the degree order of SiO2 within the biologic structures is much higher than that of outside. The impurity minerals albites are formed earlier than the original deposition. Kaolinites, feldspars and mixture of organic materials display lower degree of crystallinities and accumulate as vermicular aggregates.

  14. Emplacement age and tectonic implications of the Xilinhot A-type granite in Inner Mongolia, China

    Institute of Scientific and Technical Information of China (English)

    SHI Guanghai; MIAO Laicheng; ZHANG Fuqing; JIAN Ping; FAN Weiming; LIU Dunyi


    A new rock type of granite, approximate 45 km2 in area and located about 10 km south of Xilinhot, Inner Mongolia, was found in the Sunitezuoqi (or called Suzuoqi)-Xilinhot tectonic belt and identified as an A-type mia- rolitic intrusion. The pluton has miarolitic structure and is composed chiefly of perthite, quartz, euhedral albite and potassium feldspar. Various types of textures occur in the pluton, such as perthitie, graphic and myrmekite textures. Only quartz is found in miarolitic cavity. This A-type granite with seagull-shaped REE patterns and obvious negative Eu anomaly (δEu = 0.24-0.28) is high in SiO2 (76%-77%), K and Na (Na2O + K2O = 7.75%-8.15%) and low in Ca (CaO = 0.20%-0.22%), Fe and Mg. Both petrographical observations and chemical compositions indicate that it is an A-type granite. Zircon SHRIMP U-Pb analyses indicate that this A-type granite was emplaced at 276 ( 2 Ma and coeval with the same type of granites in the adjacent areas. Therefore, it suggests that this pluton was likely formed in a post-orogenic extensional setting and probably related to break-off of subducted slabs in Central Asian Orogenic Belt (CAOB), which indicate that the Sunitezuoqi-Xilinhot belt was tectonically evolved into post-orogenic stage since early Permian.

  15. Chemical treatment of kaolin. Case study of kaolin from the Tamazert– Jijel mine

    Directory of Open Access Journals (Sweden)

    Mohamed Chouafa


    Full Text Available The Tamazert-Jijel kaolin deposit is located in eastern Algeria, It was formed during a process of hydro-thermal alteration of feldspars rich in potassium. Kaolin, obtained at the mine, mainly contains varying amounts of impurities such as iron oxide (Fe2O3 and anatase (TiO2. These components negatively affect the quality of the commercial product. This research was performed to improve the quality of kaolin to be used in the paper industry with the goal of reducing the impurities of iron and titanium oxides. Different sized fractions of the original sample were analyzed by XRD. The results obtained showed that the mineralogical composition is: quartz, muscovite, kaolinite, dolomite, albite and orthoclase. Kaolin, like all clays, has a thin dissemination of minerals throughout it. After processing kaolin, the particle size fraction of less than 45μm, corresponding to the liberation mesh size, was retained for purification by chemical treatment with different acids of different concentrations (hydrochloric acid, sulfuric acid, acetic acid, heated to boiling point temperatures. The kaolin samples treated with the various acids above were analyzed by X-ray fluorescence and by XRD. The results obtained from the sample treated with hydrochloric acid show that the iron oxide content of acid is reduced by 1.65% to 0.88%. Meanwhile, the brightness of the sample reached 90% under the effect of the treatment with hydrochloric acid at concentration of 2 mole/dm3.

  16. Aqueous Chemistry of Typical Geothermal Springs with Deep Faults in Xinyi and Fengshun in Guangdong Province, China

    Institute of Scientific and Technical Information of China (English)

    Guoping Lu; Runfang Liu


    This paper investigated aqueous chemistry for two geothermal spring groups responsive and sensitive to flow fluctuations induced by earthquakes. Quake monitorings are favored for their be-ing in residential areas with well-preserved natural flow systems in Xinyi City’s Xijiang Hot Springs and Fengshun County’s Shihu Hot Spring. The hot springs are typical in temperatures and flow rates in southern China’s Guangdong Province. Physical and chemical conditions deep down in the heat sources are important constraints on earthquake, fluid flow, reactive solute transport and heat transfer, but re-main challenging to address via field observations and numerical experiments. In this paper, we made daily and annual observations on flow rates, temperature, and/or aqueous chemistry. We employed strontium isotopes as tracers for the water sources, equilibrium phase diagram for K-feldspar and albite stability, and Na-K-Mg diagram for heat reservoir temperatures. The abundant sulfite content in Xi-jiang Hot Springs is discussed. Our main finding are that the deep fault springs are characterized by low reduction-oxidation potential at around-200–-150 mV and relatively large daily flow variations. The re-sults provide scientific background features on the field sites regarding earthquake monitoring and pre-dictions and geothermal reservoir.

  17. Hydrothermal alteration studies of gabbros from Northern Central Indian Ridge and their geodynamic implications

    Indian Academy of Sciences (India)

    Dwijesh Ray; Catherine Mevel; Ranadip Banerjee


    Mylonitic gabbro and altered gabbro were recovered from off-axis high and corner high locations at ridge-transform intersection, adjacent to Vityaz transform fault of the slow spreading (32–35mm/yr, full spreading) Northern Central Indian Ridge. Both the varieties show signatures of extensive alteration caused due to interaction with sea water. Mylonitic gabbro represents high temperature metamorphism (∼700–800° C) and comprised of hornblende mineral which exhibits well defined foliation/gneissic appearance along with dynamically recrystallised plagioclase grains frequently intercalated with magnetite-ilmenite. Altered gabbro from corner high generally includes low temperature greenschist grade (∼300° C) mineralogical assemblages: chlorite, albite, quartz and locally magnesio hornblende. Crystal plastic deformation resulted in mylonite formation and often porphyroclasts of plagioclase and clinopyroxene grains, while altered gabbro locally exhibits cataclastic texture. Presence of Vityaz transform fault and adjacent megamullion at the weakly magmatic ridge-transform intersection and off-axis high locations prompted the present scenario very much conducive for hydrothermal circulation and further facilitate the exhumation of present suite of gabbro.

  18. Characteristics of rare earth elements of lacustrine exhalative rock in the Xiagou Formation of Lower Cretaceous in Qingxi sag, Jiuxi basin

    Institute of Scientific and Technical Information of China (English)

    WEN Huaguo; ZHENG Rongcai; GENG Wei; FAN Mingtao; WANG Manfu


    The exhalative rock occurring in the Xiagou Formation of Lower Cretaceous in Qingxi sag, Jiuxi basin is a sort of a rare lacustrine white smoke type, rich in ferrodolo-mites and albites. This paper introduces the geological back-ground, mineral association, and lithology of the exhalative rock, and discusses its REE geochemical characteristics and connection with hydrothermal environment. It is shown that the exhalative rock has basal characteristics of hydrothermal depositional formation of LREE>HREE, with positive δCe and negative δEu, which is different from the character-istics of marine exhalative rock. Since the REE pattern and exceptional distribution of δEu and δCe are highly similar to the characteristics of alkalescent tholeiitic basalt in the same layer, the exhalative rock of Xiagou Formation isconsidered to be closely related to the origin of basalt in the same horizon. The fact that the amount of REE of exhala-tive rock decreases outwards indicates that exhalative rock in the Xiagou Formation may be connected with lacustrine hydrothermal convection circulation.

  19. Processes and sources during late Variscan Dioritic-Tonalitic magmatism

    DEFF Research Database (Denmark)

    Pietranik, A.; Waight, Tod Earle


    The Gesiniec Intrusion (Strzelin Massif, East Sudetes) (~307-290 Ma) is composed predominantly of dioritic to tonalitic rocks with 87Sr/86Sr ratios ranging from 0.7069 to 0.7080 and eNd=-3.1 to -4.2, emplaced as post-collisional magmas following the Variscan orogeny. In situ Sr isotope and trace...... element analyses of plagioclase were carried out on five diorite-tonalite samples with variable whole-rock 87Sr/86Sr compositions to constrain magma sources and elucidate magma chamber processes. Plagioclase is characterized by complex zoning patterns, such as patchy zoning, asymmetrical zoning and strong...... resorption between An-rich cores and more albitic rims.The range of Sr isotopic compositions recorded in plagioclase is 0.7069-0.7091, greater than that of the whole-rocks. No change in isotopic composition is observed across resorbed core-rim boundaries, as would be expected if the resorption was caused...

  20. Characterization of rock samples localized in some sites of the Mexican Pacific coast; Caracterizacion de muestras de rocas localizadas en algunos sitios de la costa del Pacifico Mexicano

    Energy Technology Data Exchange (ETDEWEB)

    Pena, P.; Torre, J. de la; Falcon, T.; Segovia, N. [Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico); Azorin, J. [Universidad Autonoma Metropolitana-Iztapalapa C.P. 09340 Mexico D.F. (Mexico)


    Geophysical studies in zones of high seismicity have showed differences in the content of radioactive material that is used in the study of the geochemical behavior of the subsoil. In an emanometric mapping of radon in soil realized in the Mexican Pacific coast were finding distinct levels in zones with different lithology. With the finality to know the mineralization types in two zones of study which are localized in the Guerrero coast and they belonging to terrains named Guerrero and Xolapa it was determined the mineralogic characteristics in two types of rocks. The identification of the rocks was realized by X-ray diffraction and was determined the elemental chemical composition using a scanning electron microscope. It was indicated in the results obtained that in the two types of rocks were found minerals such as: quartz, albite, microcline anortite, ferroactinolite and biotite. However, it was found differences between them by the presence of their mineralogic compounds because in the rock belonging to Xolapa terrain were presented whereas in the rock localized in the Guerrero terrain were presented sodic and potassic feldspars. The analysis by the Elemental Chemical Composition technique (Energy Dispersive Spectroscopy) corroborated the results obtained by the X-ray diffraction technique. (Author)

  1. Process optimization of reaction of acid leaching residue of asbestos tailing and sodium hydroxide aqueous solution

    Institute of Scientific and Technical Information of China (English)


    Silica is the major component of the acid leaching residue of asbestos tailing. The waterglass solution can be prepared by the reaction of the residue with sodium hydroxide aqueous solution. Compared to the high temperature reaction method, this process is environmental friendly and low cost. In this paper, the reaction process of the residue and the sodium hydroxide aqueous solution is optimized. The optimum reaction process parameters are as follows: the usage of sodium hydroxide is 26.4 g/100 g acid leaching residue, the reaction temperature is 90℃, the reaction time is 1 h, and the ratio of the liquid/solid is 2.0. The significance sequence of the process parameters to the alkali leaching reaction effect is the usage of sodium hydroxide > the ratio of the liquid/solid > the reaction time > the reaction temperature. The significance sequence to the leaching ratio of SiO2 is the ratio of the liquid/solid > the usage of sodium hydroxide > the reaction time > the reaction temperature. The significance sequence to the modulus of the sodium silicate is the ratio of the liquid/solid > the usage of sodium hydroxide > the reaction time > the reaction temperature. Under the optimum conditions, the leaching ratio of the SiO2 is 77.5%, and the modulus of the sodium silicate is 3.15. The XRD analysis result indicates that the major components of the alkali leaching residue are serpentine, talc, quartz and some albite.

  2. Formation of cordierite-bearing lavas during anatexis in the lower crust beneath Lipari Island (Aeolian arc, Italy) (United States)

    Di, Martino C.; Forni, F.; Frezzotti, M.L.; Palmeri, R.; Webster, J.D.; Ayuso, R.A.; Lucchi, F.; Tranne, C.A.


    Cordierite-bearing lavas (CBL;~105 ka) erupted from the Mt. S. Angelo volcano at Lipari (Aeolian arc, Italy) are high-K andesites, displaying a range in the geochemical and isotopic compositions that reflect heterogeneity in the source and/or processes. CBL consist of megacrysts of Ca-plagioclase and clinopyroxene, euhedral crystals of cordierite and garnet, microphenocrysts of orthopyroxene and plagioclase, set in a heterogeneous rhyodacitic-rhyolitic groundmass containing abundant metamorphic and gabbroic xenoliths. New petrographic, chemical and isotopic data indicate formation of CBL by mixing of basaltic-andesitic magmas and high-K peraluminous rhyolitic magmas of anatectic origin and characterize partial melting processes in the lower continental crust of Lipari. Crustal anatectic melts generated through two main dehydration-melting peritectic reactions of metasedimentary rocks: (1) Biotite + Aluminosilicate + Quartz + Albite = Garnet + Cordierite + K-feldspar + Melt; (2) Biotite + Garnet + Quartz = Orthopyroxene + Cordierite + K-feldspar + Melt. Their position into the petrogenetic grid suggests that heating and consequent melting of metasedimentary rocks occurred at temperatures of 725 crust of Lipari was induced by protracted emplacement of basic magmas in the lower crust (~130 Ky). Crustal melting of the lower crust at 105 ka affected the volcano evolution, impeding frequent maficmagma eruptions, and promoting magma stagnation and fractional crystallization processes. ?? 2011 Springer-Verlag.

  3. The heterogeneous nature of mineral matter, fly-ash and deposits

    Energy Technology Data Exchange (ETDEWEB)

    Creelman, R.A.; Pohl, J.H.; Devir, G.P.; Su, S. [R.A. Creelman and Associates, Epping, NSW (Australia)


    This paper reports on a series of slagging studies investigating the heterogeneous nature of mineral matter, fly ash and deposits, and how this heterogeneity affects deposition. The data come from low temperature ashing (LTA) of pulverised coal, fly ash from boilers, and deposits from pilot-scale furnaces and boilers. The paper presents optical and scanning electron (SEM) micrographs, electron microprobe analysis (EMPA) and energy dispersive x-ray analysis (EDXRA) of mineral matter, individual fly ash particles, and localised regions of deposits. During combustion, the included mineral matter is transformed into fly ash, melts and partially adheres to the char surface, and may form agglomerated masses. Excluded mineral matter has little chance of encountering another ash particle and agglomerating in the gas phase, but can react with other particles in the wall deposits. Certain fly ash particles adhere to the wall where they can combine with other fly ash particles. Analyses of molten regions of deposits have shown, so far, four mineral phase fields to be responsible for forming difficult deposits with melting points below deposit surface temperatures of 1200 to 1350{sup o}C. These mineral fields include iron cordierite, albite and its silica undersaturated equivalent nepheline, anorthite, and compounds with ratios of Ca to P of 2.3-2.5.

  4. Mineralization Zoning in Yindongzi—Daxigou Barite—Siderite,Silver—Polymetallic Deposits in the Qinling Orogen,China

    Institute of Scientific and Technical Information of China (English)

    方维萱; 胡瑞忠; 等


    The Yindongzi-Daxigou strata-bound barite-siderite,silver-polymetallic deposits discovered in the Qinling orogen are hosted within flysch facies in a deep-water fault-controlled basin on the passive northern margin of the Qinling microplate.The orebodies occur in a series of hydrothermal depositonal rocks.Mineralization zoning is characterized by Fe-Ba←Ba-Cu←Pb-Ab→Cu-Ag→Pb→Au.This is obviously a gradational transition mineralization from ventproximal mineralization to more distal mineralization.In this gradational transition between Chefanggou and Yindongzi,vent-proximal mineralization consists of silver-polymetallic orebodies(Pb-Ag),which is the center of hydrothermal mineralization.The Chefanggou Ba-Cu ore district in the west and the Yindongzi Cu-Ag ore district in the east represent vent lateral mineralization.Distal mineralization in the west is represented by the Daxigou Fe-Ba ore district while distal mineralization in te east is represented by the Pb ore district.Thick massive,laminated barren albite chert and jasperite,sometimes with minor silver-ploymetallic mineralization of commercial importance,and pyritization in rocks feature more distal mineralization.Geochemical anomalies of Au-As associations are found in ankerite phyllite and muddy sandstone.Actually,Au deposits are dominantly controlled by the late brittle-ductile shear zone.

  5. Mineralization Zoning in Yindongzi-Daxigou Barite-Siderite, Silver-Polymetallic Deposits in the Qinling Orogen, China

    Institute of Scientific and Technical Information of China (English)

    方维萱; 胡瑞忠; 黄转莹


    The Yindongzi-Daxigou strata-bound barite-siderite, silver-polymetallic deposits discovered in the Qinling orogen are hosted within flysch facies in a deep-water fault-controlled basin on the passive northern margin of the Qinling microplate. The orebodies occur in a series of hydrothermal depositional rocks. Mineralization zoning is characterized by Fe-Ba←Ba-Cu←Pb-Ag→Cu-Ag→Pb→Au. This is obviously a gradational transition mineralization from ventproximal mineralization to more distal mineralization. In this gradational transition between Chefanggou and Yindongzi, vent-proximal mineralization consists of silver-polymetallic orebodies (Pb-Ag), which is the center of hydrothermal mineralization. The Chefanggou Ba-Cu ore district in the west and the Yindongzi Cu-Ag ore district in the east represent vent lateral mineralization. Distal mineralization in the west is represented by the Daxigou Fe-Ba ore district while distal mineralization in the east is represented by the Pb ore district. Thick massive, laminated barren albite chert and jasperite, sometimes with minor silver-ploymetallic mineralization of commercial importance, and pyritization in rocks feature more distal mineralization. Geochemical anomalies of Au-As associations are found in ankerite phyllite and muddy sandstone.Actually, Au deposits are dominantly controlled by the late brittle-ductile shear zone.

  6. Diagenetic Reactions in Reservoir Strata and Geochemical Properties of Pore Fluid and Its Origin in Songlian Basin

    Institute of Scientific and Technical Information of China (English)

    楼章华; 蔡希源; 等


    The reservoirs of the SOngliao Basin are composed of typical unstable sandstones,with high percentages of volcanic fragments and feldspar,In the course of sedimentation and burying,a series of physical and chemical reactions took place between minerals and pore water and water-rock reactions and ion exchange caused changes in ion assemblage of pore water,Hydration-hydrolysis,dissolution and the albitization of feldspar made many ions free from their framework and inter into the pore water,and induced the precipitation of a large amount of authigenic minerals such as smectite and chlorite,During the diagenesis of sandstone.diagenetic reactions involved several stages with increasing depth,and so did the precipitation of authigenic minerals and the transformaiton of minerals.The migration of ions is related with the precipitation,transformation and dissolution of authigenic minerals.Thus,to deepen our study on sandstone diagenesis is an important link for the analysis of ion migration in the evolution of pore water ,the origin and evolution of pore water could be tracked in terms of the geochemistry of fluid inclusions in authigenic minerals.And the isotopic composition of the authigenic mineral calcite can provide its genetic information.

  7. Zircon syenite pegmatites in the Finero peridotite (Ivrea zone): evidence for a syenite from a mantle source

    Energy Technology Data Exchange (ETDEWEB)

    Staehle, V.; Frenzel, G. (Mineralogisch-Petrographisches Inst., Univ. Heidelberg (Germany, F.R.)); Kober, B. (Lab. fuer Geochronologie, Univ. Heidelberg (Germany, F.R.)); Michard, A. (Centre de Recherches Petrographiques et Geochimiques, 54 - Vandoeuvre (France)); Puchelt, H. (Inst. fuer Petrographie und Geochemie, Univ. Karlsruhe (Germany, F.R.)); Schneider, W. (Inst. fuer Geologie und Palaeontologie, Technische Univ. Braunschweig (Germany, F.R.))


    Zircon syenite pegmatite dikes in the phlogopite peridotite of Finero are rich in volatiles, incompatible elements and in rare earths with (La/Yb){sub N} ratios in the range of 14-15. The main mineral constituents in the alkaline dikes (Na>K) are albite and magnesium-rich biotites whereas nepheline, cancrinite, sodalite, zircon and apatite are minor or accessory. With their initial {sup 87}Sr/{sup 86}Sr ratio of 0.70371 the non-contaminated syenite pegmatites originate from partial melts of the upper mantle. The magma is derived from a depleted mantle source with isotopic signatures ({epsilon}Nd(T)=5.7 and 5.1) of ocean island basalts (OIB). The ascent of the syenite pegmatites and the marginal uplift of the granulitic crust in the northern Ivrea zone may be correlated with the intrusion of alkaline melts at depth. The Triassic zircon age of 225+-13 Ma is interpreted as the time of the dikes' emplacement. From geochemistry and setting it is concluded, that the syenites are related to a rift magmatic stage at the early Mesozoic in the southern Alps. (orig.).

  8. Emplacement of pyroclastic density currents (PDCs) in a deep-sea environment: The Val d'Aveto Formation case (Northern Apennines, Italy) (United States)

    Di Capua, Andrea; Groppelli, Gianluca


    The occurrence of PDC deposits in a foredeep basin sequence, named Val d'Aveto Formation (32-29 Ma, Northern Apennines, Italy), provides new information on the behavior of pyroclastic density currents entering the water. In this work, stratigraphic, petrographic and mineralogical features that characterize three pyroclastic deposits have been described and analyzed in the field (facies and lithological analysis on the blocky-size fraction) and in the laboratory (image analyses on the blocky-size detritus, optical analyses of the microtextures, mineralogical analyses through X-ray powder diffraction (XRPD) and scanning electron microscope with energy dispersive X-ray spectometry (SEM-EDS). The deposits are lapilli- to blocky-size, with a blocky-size fraction constituted of accidental detritus. In thin sections, their groundmass texture varies from porphyritic to eutaxitic where coarser particles become close each others. Growth rims have been also detected around plagioclase crystals. Pyrite habits and oxidation, and plagioclase albitization are consistent with hydrothermal temperature conditions of 200 °C. All these results have been compared with the information provided by modern examples of PDC deposits and laboratory experiments on the behavior of water/hot particles mixing. Grain-to-grain collision has been considered as the main flow mechanism that sustained and avoided the disaggregation of the PDCs entering the water.

  9. Facies metamórficas y edades relativas de las rocas del extremo oriental del Brazo Huemul, provincia de Neuquén Metamorphic facies and relative ages of rocks on the eastern part of Brazo Huemul, Neuquén province

    Directory of Open Access Journals (Sweden)

    M.F. Gargiulo


    exposed in the study area are mainly of tonalitic composition and have been correlated with the Subcordilleran Patagonian Batholith because they are crosscut by two different types of dikes. One group of dikes shows an albite - chlorite - epidote - cummingtonite/ grunerite - hornblende mineral assemblage as a consequence of a thermal metamorphic event transitional between albite - epidote hornfels facies and hornblende hornfels conditions. This process has been attributed to the emplacement of the Cordilleran Patagonian Batholith of Cretaceous age. Because of this, the hornfels dikes were correlated with Montes de Oca Formation. The other group of dikes shows a chlorite + pumpellyite + laumontite + chlorite/esmectite + iron oxides assemblage indicating metamorphism in zeolite facies of high temperature or, sometimes shows propilitic alteration and these dikes have been correlated with the Ventana Formation. The differences between these two types of dikes allow the discussion of the relative age of the tonalitic rocks that host them. In this paper it is proposed that this tonalitic body is of Low to Middle Jurassic age.

  10. Northwest Africa 6693: A new type of FeO-rich, low-Δ17O, poikilitic cumulate achondrite (United States)

    Warren, Paul H.; Rubin, Alan E.; Isa, Junko; Brittenham, Steve; Ahn, Insu; Choi, Byeon-Gak


    Northwest Africa 6693 is a new type of achondrite, with a unique combination of oxygen-isotopic composition (low Δ17O: -1.08‰; also δ17O = 1.19‰) and FeO-rich, low mg bulk composition. A mode (in vol%) shows 70% pyroxene, 16% olivine and 13% feldspar, along with 0.6% Cr-spinel, and 0.4% NiFe metal (awaruite). Its coarse-poikilitic texture, with pigeonite oikocrysts up to 14 mm, as well as the subchondritic MgO/SiO2 of the rock's bulk composition, indicate origin as an igneous cumulate. The cumulus phases included pigeonite and olivine, and the parent magma was probably also saturated with feldspar, which occurs mainly as anhedral, yet optically continuous, grains intergrown with the pyroxene. The mafic silicates are uniformly ferroan: pigeonite near En57Wo3.2 and olivine near Fo49. The feldspar is uniformly albitic, near Ab92, except for a single tiny grain of Ab57Or43. However, the albite features diverse K/Ca (Or/An) ratios: ranging from consistently ˜0.46 in one end of the oblong NWA 6693 stone, to 5.2 in an olivine-rich enclave that consists mostly of micrographic olivine-feldspar intergrowth. Also, siderophile and incompatible element data show heterogeneity among samples from different regions of this large cumulate. The rock was probably neither an orthocumulate nor an adcumulate, and the proportion of "trapped liquid" probably varied from place to place. After initial crystallization, a shock event caused very minor brecciation, and pervasively mobilized linear-arcuate trails of microinclusions (minute oxides, mostly) and bubbles. A minor proportion of additional melt was formed within, and/or infiltrated into, the rock and formed discrete overgrowth mantles, recognizable based on unusual scarcity of microinclusions, on some pyroxenes. Final cooling, based on mineral-equilibration temperatures, occurred at a moderate rate by intrusive-igneous standards. Olivine, metal, and sulfide phases are all very Ni-rich (e.g., olivine NiO averages 0.77 wt

  11. Variations in the chemical and stable isotope composition of carbon and sulfur species during organic-rich sediment alteration: An experimental and theoretical study of hydrothermal activity at guaymas basin, gulf of california (United States)

    Seewald, Jeffrey S.; Seyfried, William E., Jr.; Shanks, Wayne C., III


    Organic-rich diatomaceous ooze was reacted with seawater and a Na-Ca-K-Cl fluid of seawater chlorinity at 325-400°C, 400-500 bars, and fluid/sediment mass ratios of 1.56-2.35 to constrain factors regulating the abundance and stable isotope composition of C and S species during hydrothermal alteration of sediment from Guaymas Basin, Gulf of California. Alteration of inorganic and organic sedimentary components resulted in extensive exchange reactions, the release of abundant H 2S, CO 2, CH 4, and C organic, to solution, and recrystallization of the sediment to an assemblage containing albitic plagioclase, quartz, pyrrhotite, and calcite. The δ 34S cdt values of dissolved H 2S varied from -10.9 to +4.3‰ during seawater-sediment interaction at 325 and 400°C and from -16.5 to -9.0‰ during Na-Ca-K-Cl fluid-sediment interaction at 325 and 375°C. In the absence of seawater SO 4, H 2S is derived from both the transformation of pyrite to pyrrhotite and S released during the degradation of organic matter. In the presence of seawater SO 4, reduction of SO 4 contributes directly to H 2S production. Sedimentary organic matter acts as the reducing agent during pyrite and SO 4 reduction. Requisite acidity for the reduction of SO 4 is provided by Mg fixation during early-stage sediment alteration and by albite and calcite formation in Mg-free solutions. Organically derived CH 4 was characterized by δ 13C pdb values ranging between -20.8 and -23.1‰, whereas δ 13C pdb values for dissolved C organic ranged between -14.8 and -17.7%. Mass balance calculations indicate that δ13C values for organically derived CO 2 were ≥ - 14.8%. Residual solid sedimentary organic C showed small (≤ 0.7‰) depletions in 13C relative to the starting sediment. The experimental results are consistent with the isotopic and chemical composition of natural hydrothermal fluids and minerals at Guaymas Basin and permit us to better constrain sources and sinks for C and S species in subseafloor

  12. Caracterización hidroquímica y análisis de los estados de equilibrio termodinámico en aguas termominerales de Alhama de Murcia (Murcia, Espana

    Directory of Open Access Journals (Sweden)

    Padilla Benítez, A.


    Full Text Available The principal physico-chemical characteristics of sorne thermomineral waters of Alhama de Murcia detrital aquifer are studied. The waters show a temperature between 26-41 °C and they are calcium-magnesium chloride-sulphate type. The origin of ions has a direct relationship with the dissolution of evaporitic sulphate-chloride salts, carbonatic and silica rocks, agricultural contamination processes and possibly ore-deposits. Mixing processes with cold waters possibly also occur. By SOLMINEQ.88 program the thermodinamic equilibrium conditions in surface are studied; the samples are saturated in quartz, chalcedony and albite. A great part of the waters are also saturated in calcite, aragonite, dolomite, gypsum, barite and magnesite. Finally, the waters are undersaturated in cristobalite, anhydrite and fluorite. Conventional chemical geothermometers yield a broad range of temperatures. Both, calcite-dolomite and anhydrite-fluorite geothermometers was applied to two samples with anomalous results. The saturation index modeling, at a series of growing temperatures, shows an approach equilibrium with quartz, chalcedony, albite, sanidine, gipsum, anhydrite, gibbsite and halloisite between 80-110 °C. A spread in the apparent equilibration temperatures deduced from two metodology, should be a consequence of dilution by surface waters, effects of re-equilibration of minerals with waters and CO2 loss. Temperature and chemical composition of the waters shows a thermal anomaly directly related with the tectonic activity in the area.Se estudian las principales características físico-químicas de algunas aguas termominerales del acuífero detrítico de Alhama de Murcia cuya temperatura está comprendida entre 26 y 41 °C y son de facies clorurada-sulfatada cálcico-magnésica. El origen de los iones encontrados está relacionado con la disolución de materiales evaporíticos, sales sulfatadas y cloruradas, carbonatados y silicatados, procesos de

  13. Metal-rich fluid inclusions provide new insights into unconformity-related U deposits (Athabasca Basin and Basement, Canada) (United States)

    Richard, Antonin; Cathelineau, Michel; Boiron, Marie-Christine; Mercadier, Julien; Banks, David A.; Cuney, Michel


    The Paleoproterozoic Athabasca Basin (Canada) hosts numerous giant unconformity-related uranium deposits. The scope of this study is to establish the pressure, temperature, and composition (P-T-X conditions) of the brines that circulated at the base of the Athabasca Basin and in its crystalline basement before, during and after UO2 deposition. These brines are commonly sampled as fluid inclusions in quartz- and dolomite-cementing veins and breccias associated with alteration and U mineralization. Microthermometry and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) data from five deposits (Rabbit Lake, P-Patch, Eagle Point, Millennium, and Shea Creek) complement previously published data for the McArthur River deposit. In all of the deposits investigated, fluid inclusion salinity is between 25 and 40 wt.% NaCl equiv., with compositions displaying a continuum between a "NaCl-rich brine" end-member (Cl > Na > Ca > Mg > K) and a "CaCl2-rich brine" end-member (Cl > Ca ≈ Mg > Na > K). The CaCl2-rich brine has the highest salinity and shows evidence for halite saturation at the time of trapping. The continuum of compositions between the NaCl-rich brine and the CaCl2-rich brine end-members combined with P-T reconstructions suggest anisothermal mixing of the two brines (NaCl-rich brine, 180 ± 30 °C and 800 ± 400 bars; CaCl2-rich brine, 120 ± 30 °C and 600 ± 300 bars) that occurred under fluctuating pressure conditions (hydrostatic to supra-hydrostatic). However, because the two brines were U bearing and therefore oxidized, brine mixing was probably not the driving force for UO2 deposition. Several scenarios are put forward to account for the Cl-Na-Ca-Mg-K composition of the brines, involving combinations of seawater evaporation, halite dissolution, mixing with a halite-dissolution brine, Mg/Ca exchange by dolomitization, Na/Ca exchange by albitization of plagioclase, Na/K exchange by albitization of K-feldspar, and Mg loss by Mg


    Institute of Scientific and Technical Information of China (English)

    李雪芳; 唐茂; 刘耘


    This study provided a number of theoretical equilibrium isotope fractionations between several Ge species, including quartz- (or opal-), albite-, K-feldspar- and olivine-like structures, as well as the dominant Ge(OH)4 and GeO(OH)3- species in aqueous solutions. They are basic parameters for exploring the unknown application of Ge isotope in the field of geochemistry. Our method is based on the Urey model (or the Bigeleisen-Mayer equation) and quantum chemistry calculation. We estimated that the accuracy of the parameters could be around 0.3‰, with the calculations made at B3LYP/6-311+G(d,p) level. Solvent effect was handled using explicit solvent model ("water droplet" method), and the minerals were simulated by cluster model. Our results showed that quartz- or opal-like structure can enrich most heavy Ge isotopes, and at 25℃, the fractionations are around Δquartz-Ge(OH)4=0.9‰, ΔGe(OH)4-GeO(OH)3-=0.3‰ (in seawaters), Δquartz-albite=0.6‰, Δquartz-K-feldspar=0.4‰, Δolivine-Ge(OH)4=-1.2‰ and Δquartz-olivine=2.1‰. These data could give better explanations to the experimental observations of Siebert et al. (2006) and Rouxel et al. (2006), suggesting that our theoretical prediction is accurate and important for real geochemical problems.%本研究基于Urey模型(或称Bigeleisen和Mayer公式),结合量子化学计算的方法,在B3LYP/6-311+G(d, p)理论水平下,计算了Ge在类似石英(包括蛋白石)、钠长石、钾长石、橄榄石结构以及水溶液(包括海水)中Ge(OH)4和GeO(OH)3-之间的Ge同位素平衡分馏系数.其中,溶液效应用"水滴法"处理,矿物结构用簇合物方法模拟.结果显示这些基本分馏参数的精度约±0.3‰;类石英(或蛋白石)结构最可能富集重Ge同位素,在25 ℃,几个Ge同位素分馏系数分别约为:Δ石英-Ge(OH)4=0.9‰、ΔGe(OH)4-GeO(OH)3-=0.3‰(海水中)、Δ石英-钠长石=0.6‰、Δ石英-钾长石=0.4‰、Δ橄榄石-Ge(OH)4=-1.2‰.类石英与类橄榄

  15. Inverse Geochemical Reaction Path Modelling and the Impact of Climate Change on Hydrologic Structure in Snowmelt-Dominated Catchments in the Southwestern USA (United States)

    Driscoll, J. M.; Meixner, T.; Molotch, N. P.; Sickman, J. O.; Williams, M. W.; McIntosh, J. C.; Brooks, P. D.


    Snowmelt from alpine catchments provides 70-80% of the American Southwest's water resources. Climate change threatens to alter the timing and duration of snowmelt in high elevation catchments, which may also impact the quantity and the quality of these water resources. Modelling of these systems provides a robust theoretical framework to process the information extracted from the sparse physical measurement available in these sites due to their remote locations. Mass-balance inverse geochemical models (via PHREEQC, developed by the USGS) were applied to two snowmelt-dominated catchments; Green Lake 4 (GL4) in the Rockies and Emerald Lake (EMD) in the Sierra Nevada. Both catchments primarily consist of granite and granodiorite with a similar bulk geochemistry. The inputs for the models were the initial (snowpack) and final (catchment output) hydrochemistry and a catchment-specific suite of mineral weathering reactions. Models were run for wet and dry snow years, for early and late time periods (defined hydrologically as 1/2 of the total volume for the year). Multiple model solutions were reduced to a representative suite of reactions by choosing the model solution with the fewest phases and least overall phase change. The dominant weathering reactions (those which contributed the most solutes) were plagioclase for GL4 and albite for EMD. Results for GL4 show overall more plagioclase weathering during the dry year (214.2g) than wet year (89.9g). Both wet and dry years show more weathering in the early time periods (63% and 56%, respectively). These results show that the snowpack and outlet are chemically more similar during wet years than dry years. A possible hypothesis to explain this difference is a change in contribution from subsurface storage; during the wet year the saturated catchment reduces contact with surface materials that would result in mineral weathering reactions by some combination of reduced infiltration and decreased subsurface transit time. By

  16. Petrography and U-Pb Zircon Geochronology of Geological Units of the Mesa de Cocodite, Península de Paraguaná, Venezuela (United States)

    Mendi, D.; Baquero, M. L.; Oliveira, E. P.; Urbani, F.; Pinto, J.; Grande, S.; Valencia, V.


    Several continental crust units crop out in The Mesa de Cocodite, central Paraguaná Peninsula, Northwestern Venezuela, including a newly mapped quartz-feldspar gneiss that intruded the El Amparo Pluton, a major low-graded metamorphic unit of Permian age. It is unconformably overlying by Late Jurassic phyllites of the Pueblo Nuevo Formation. All these units are cross-cut by narrow dykes. This contribution focuses on the petrography and LA-ICP-MS U-Pb zircon dating of the igneous units, with the aim of constraining magmatism and its tectonic significance in the area. The quartz-feldspar gneiss consists of albite, bluish-smoked quartz, muscovite-chlorite, epidote and zircon. The enclosing El Amparo Pluton is typically a coarse-grained and thick-banded metagranodiorite, containing andesine, quartz, hornblende, epidote, K-feldspar, biotite, chlorite, titanite and zircon. The younger dykes consist of fine-grained, porphyritic hornblende diorites that contain numerous hornblende phenocrysts. The main minerals are andesine, hornblende, quartz, and chlorite. Accessory minerals include zircon, epidote and opaques. A felsic gneiss xenolith collected from the dykes contain quartz, K-feldspar, chlorite, epidote, albite and zircon. Zircon population in the quartz-feldspar gneiss displays a discordia trend, ranging in age from 1050-750 Ma but mostly around 950-900 Ma, which may represent a peak high-grade metamorphism in the area. The El Amparo Pluton provides a concordant Permian age (271.3±6.5 Ma), which is comparable with previous reported U-Pb ages in titanite. Because the porphyry dykes cross-cut all the units in the area, they should be post-Late Jurassic in Age; however, all dated zircons from the dykes are in the range of 1200-750 Ma. The absence of younger ages can be attributed to either formation during a relatively low temperature magmatic event, which generated very narrow younger zircon rims only and thus undetectable with the technique used, or a completely lack

  17. Apatite at Olympic Dam, South Australia: A petrogenetic tool (United States)

    Krneta, Sasha; Ciobanu, Cristiana L.; Cook, Nigel J.; Ehrig, Kathy; Kontonikas-Charos, Alkis


    The > 10,000 million tonne Olympic Dam Cu-Au-U-Ag deposit, (eastern Gawler Craton, South Australia) is one of the largest orebodies in the World. The deposit is hosted within the Olympic Dam Breccia Complex, placed at the centre of, and resulting from multiple brecciation and Fe-metasomatism of the Roxby Downs Granite (RDG). The latter is part of a larger batholith emplaced at ~ 1.6 Ga. Apatite petrography and chemistry were studied in non-mineralised RDG and coeval granitoids and dolerites, as well as in mineralised RDG from deep (> 2 km) and distal (2.7 km to NE) locations. In both latter cases, although the mineralisation corresponds to the same, early chalcopyrite-pyrite-magnetite ± hematite stage identified in the outer and deeper zones of the deposit itself, the character of granite alteration differs: sericite-chlorite alteration with all feldspar replaced in the deep location; and red-stained K-feldspar on top of prevailing albitization in the distal location. Close-to end-member fluorapatite is a key accessory mineral in all igneous rocks and a common product of early hydrothermal alteration within mineralised granite. Variations in habit, morphology and textures correlate with chemical trends expressed as evolving Cl/F ratios, and concentrations of REE + Y (hereafter REY), Sr, Mn, S, Si and Na. Magmatic apatite is unzoned in the dolerite but features core to REY-enriched rim zonation in the granitoids. Increases in Cl- and Sr-contents correlate with rock basicity. Calculation of Cl in the vapour phase relative to melt at the apatite saturation temperature for zoned apatite in the RDG shows higher values for grains with inclusion-rich cores associated with mafic enclaves, concordant with assimilation of exotic material during magma crystallisation. Hydrothermal alteration of magmatic apatite is most varied in the dolerite where interaction with fluids is expressed as subtle changes in Cl- versus F- and REY-enrichment, and most importantly, S-enrichment in

  18. Ages and sources of components of Zn-Pb, Cu, precious metal, and platinum group element deposits in the goodsprings district, clark county, Nevada (United States)

    Vikre, P.; Browne, Q.J.; Fleck, R.; Hofstra, A.; Wooden, J.


    ore breccias and relatively low S and Pb isotope values (??34S values vary from 0-??4%; 206Pb/204Pb replaced breccia clasts and margins of fissures in Paleozoic limestones and dolomites near porphyritic intrusions. Gold ?? silver deposits occur along contacts and within small-volume stocks and dikes of feldspar porphyry, one textural variety of porphyritic intrusions. Lead isotope compositions of copper ?? precious metal-PGE, gold ?? silver, and lead-dominant carbonate replacement deposits are similar to those of Mojave crust plutons, indicating derivation of Pb from 1.7 Ga crystalline basement or from Late Proterozoic siliciclastic sedimentary rocks derived from 1.7 Ga crystalline basement. Four texturally and modally distinctive porphyritic intrusions are exposed largely in the central part of the district: feldspar quartz porphyry, plagioclase quartz porphyry, feldspar biotite quartz porphyry, and feldspar porphyry. Intrusions consist of 64 to 70 percent SiO2 and variable K2O/Na2O (0.14-5.33) that reflect proportions of K-feldspar and albite phenocrysts and megacrysts as well as partial alteration to K-mica; quartz and biotite phenocrysts are present in several subtypes. Albite may have formed during emplacement of magma in brine-saturated basinal strata, whereas hydrothermal alteration of matrix, phenocrystic, and megacrystic feldspar and biotite to K-mica, pyrite, and other hydrothermal minerals occurred during and after intrusion emplacement. Small volumes of garnet-diopside-quartz and retrograde epidote-mica-amphibole skarn have replaced carbonate rocks adjacent to one intrusion subtype (feldspar-quartz porphyry), but alteration of carbonate rocks at intrusion contacts elsewhere is inconsp. Uranium-lead ages of igneous zircons vary inconsistently from ?? 180 to 230

  19. Experimental constraints on the relative stabilities of the two systems monazite-(Ce) - allanite-(Ce) - fluorapatite and xenotime-(Y) - (Y,HREE)-rich epidote - (Y,HREE)-rich fluorapatite, in high Ca and Na-Ca environments under P-T conditions of 200-1000 MPa and 450-750 °C (United States)

    Budzyń, Bartosz; Harlov, Daniel E.; Kozub-Budzyń, Gabriela A.; Majka, Jarosław


    The relative stabilities of phases within the two systems monazite-(Ce) - fluorapatite - allanite-(Ce) and xenotime-(Y) - (Y,HREE)-rich fluorapatite - (Y,HREE)-rich epidote have been tested experimentally as a function of pressure and temperature in systems roughly replicating granitic to pelitic composition with high and moderate bulk CaO/Na2O ratios over a wide range of P-T conditions from 200 to 1000 MPa and 450 to 750 °C via four sets of experiments. These included (1) monazite-(Ce), labradorite, sanidine, biotite, muscovite, SiO2, CaF2, and 2 M Ca(OH)2; (2) monazite-(Ce), albite, sanidine, biotite, muscovite, SiO2, CaF2, Na2Si2O5, and H2O; (3) xenotime-(Y), labradorite, sanidine, biotite, muscovite, garnet, SiO2, CaF2, and 2 M Ca(OH)2; and (4) xenotime-(Y), albite, sanidine, biotite, muscovite, garnet, SiO2, CaF2, Na2Si2O5, and H2O. Monazite-(Ce) breakdown was documented in experimental sets (1) and (2). In experimental set (1), the Ca high activity (estimated bulk CaO/Na2O ratio of 13.3) promoted the formation of REE-rich epidote, allanite-(Ce), REE-rich fluorapatite, and fluorcalciobritholite at the expense of monazite-(Ce). In contrast, a bulk CaO/Na2O ratio of ~1.0 in runs in set (2) prevented the formation of REE-rich epidote and allanite-(Ce). The reacted monazite-(Ce) was partially replaced by REE-rich fluorapatite-fluorcalciobritholite in all runs, REE-rich steacyite in experiments at 450 °C, 200-1000 MPa, and 550 °C, 200-600 MPa, and minor cheralite in runs at 650-750 °C, 200-1000 MPa. The experimental results support previous natural observations and thermodynamic modeling of phase equilibria, which demonstrate that an increased CaO bulk content expands the stability field of allanite-(Ce) relative to monazite-(Ce) at higher temperatures indicating that the relative stabilities of monazite-(Ce) and allanite-(Ce) depend on the bulk CaO/Na2O ratio. The experiments also provide new insights into the re-equilibration of monazite-(Ce) via fluid

  20. Variations in the chemical and stable isotope composition of carbon and sulfur species during organic-rich sediment alteration: An experimental and theoretical study of hydrothermal activity at guaymas basin, gulf of california (United States)

    Seewald, Jeffrey S.; Seyfried, W.E.; Shanks, Wayne C.


    Organic-rich diatomaceous ooze was reacted with seawater and a Na-Ca-K-Cl fluid of seawater chlorinity at 325-400??C, 400-500 bars, and fluid/sediment mass ratios of 1.56-2.35 to constrain factors regulating the abundance and stable isotope composition of C and S species during hydrothermal alteration of sediment from Guaymas Basin, Gulf of California. Alteration of inorganic and organic sedimentary components resulted in extensive exchange reactions, the release of abundant H2S, CO2, CH4, and Corganic, to solution, and recrystallization of the sediment to an assemblage containing albitic plagioclase, quartz, pyrrhotite, and calcite. The ??34Scdt values of dissolved H2S varied from -10.9 to +4.3??? during seawater-sediment interaction at 325 and 400??C and from -16.5 to -9.0??? during Na-Ca-K-Cl fluid-sediment interaction at 325 and 375??C. In the absence of seawater SO4, H2S is derived from both the transformation of pyrite to pyrrhotite and S released during the degradation of organic matter. In the presence of seawater SO4, reduction of SO4 contributes directly to H2S production. Sedimentary organic matter acts as the reducing agent during pyrite and SO4 reduction. Requisite acidity for the reduction of SO4 is provided by Mg fixation during early-stage sediment alteration and by albite and calcite formation in Mg-free solutions. Organically derived CH4 was characterized by ??13Cpdb values ranging between -20.8 and -23.1???, whereas ??13Cpdb values for dissolved Corganic ranged between -14.8 and -17.7%. Mass balance calculations indicate that ??13C values for organically derived CO2 were ??? - 14.8%. Residual solid sedimentary organic C showed small (??? 0.7???) depletions in 13C relative to the starting sediment. The experimental results are consistent with the isotopic and chemical composition of natural hydrothermal fluids and minerals at Guaymas Basin and permit us to better constrain sources and sinks for C and S species in subseafloor hydrothermal systems

  1. Plagioclase deformation in upper-greenschist facies meta-pegmatite mylonites from the Austroalpine Matsch Unit (Eastern Alps, Italy) (United States)

    Eberlei, Tobias; Habler, Gerlinde; Abart, Rainer; Grasemann, Bernhard


    Feldspars are common rock forming minerals as they are stable over a wide range of bulk rock compositions and metamorphic conditions within the Earth's crust. The deformation mechanisms of feldspar play an important role in rheological models for the crust and therefore have received considerable attention in studies on natural rocks and in experimental studies. The interaction of frictional and viscous deformation mechanisms and the onset of crystal plastic deformation in feldspars occur over a broad range of pressures and temperatures. In this work, we present new microstructural, textural and mineral chemical data of plagioclase from Permian metapegmatites within the Austroalpine Matsch Unit in Southern Tyrol (Italy). These crystalline basement rocks were deformed and metamorphosed at conditions close to the greenschist/amphibolites facies transition at 480±26°C during the Cretaceous (Habler et al., 2009). The investigated samples have been collected from meter-scale shear zones which typically occur at boundaries of lithological subunits. The southern tectonic boundary of this unit is commonly referred to as the "Vinschgau Shear Zone" (Schmid & Haas, 1989). We applied the Electron Backscatter Diffraction method to investigate the grain- and subgrain-boundaries and the nature of effective deformation mechanisms in plagioclase. Large albite porphyroclasts in the mylonitic Permian metapegmatites show grain internal traces of dissolution surfaces and the formation of new, strain-free grains with straight grain boundary segments and partly 120° grain boundary triple junctions in dilatant sites. The aggregates of new grains neither have a lattice preferred orientation nor a crystallographic orientation relation with the adjacent clast, and are characterized by the lack of grain internal deformation, suggesting that these are new precipitates rather than clast-fragments or recrystallized subgrains. Furthermore, the porphyroclasts show cracks and kinks, associated

  2. Petrogenesis of pillow basalts from Baolai in southwestern Taiwan (United States)

    Liu, Chih-Chun; Yang, Huai-Jen


    The pillow basalts from Baolai in southwestern Taiwan have been inferred to bear Dupal signautres based on their Th/Ce ratio, linking the Baolai basalts to the South China Sea (SCS) seamounts that are characterized by Dupal Pb isotope signatures (Smith and Lewis, 2007). In this study, thirty-two Baolai basalt samples were analyzed for abundances of major and trace elements as well as Pb and Nd isotope ratios to verify their Dupal characters and to constrain their petrogenesis significance. The Baolai basalts contain 4-10 % L.O.I.. Three stages of alteration are inferred from plots of L.O.I. abundance versus concentrations major oxides as well as mineral textures and compositions. The first alteration stage was characterized by albitization that converted Ca-rich plagioclase to albite. The second alteration stage was dominated by chloritization of olivine and augite, resulting in increases in L.O.I. abundance. The last alteration stage is represented by formation of secondary calcite in vesicles and cracks. These alteration processes reflect interaction with seawater and apparently did not affect the magmatic Pb isotope composition for the low Pb concentration in seawater. Relative to the North Hemisphere Reference Line (NHRL), the Baolai pillow basalts have higher 208Pb/204Pb ratios at a given 206Pb/204Pb value, showing Dupal anomaly. For their relatively higher 208Pb/204Pb, 207Pb/204Pb, and 206Pb/204Pb ratios, the Baolai basalts are distinct from majority of the Cenozoic basalts in the Hainan-Leizhou peninsula, the Indochina peninsula, and the SCS seamounts, for which derivation from the Hainan mantle plume has been recently proposed (Wang et al., 2013). In contrast, the Baolai basalts and the Cenozoic basalts from eastern Guangdong at southeastern China have similar Pb and Nd isotope compositions, indicating derivation from similar mantle sources. However, the Baolai basalts have lower abundance ratios of Zr/Hf (40.3-45.6 versus 46.5-50.5), La/Yb (12

  3. Mount St. Augustine volcano fumarole wall rock alteration: Mineralogy, zoning, composition and numerical models of its formation process (United States)

    Getahun, A.; Reed, M.H.; Symonds, R.


    Intensely altered wall rock was collected from high-temperature (640??C) and low-temperature (375??C) vents at Augustine volcano in July 1989. The high-temperature altered rock exhibits distinct mineral zoning differentiated by color bands. In order of decreasing temperature, the color bands and their mineral assemblages are: (a) white to grey (tridymite-anhydrite); (b) pink to red (tridymite-hematite-Fe hydroxide-molysite (FeCl3) with minor amounts of anhydrite and halite); and (c) dark green to green (anhydrite-halite-sylvite-tridymite with minor amounts of molysite, soda and potash alum, and other sodium and potassium sulfates). The alteration products around the low-temperature vents are dominantly cristobalite and amorphous silica with minor potash and soda alum, aphthitalite, alunogen and anhydrite. Compared to fresh 1986 Augustine lava, the altered rocks exhibit enrichments in silica, base metals, halogens and sulfur and show very strong depletions in Al in all alteration zones and in iron, alkali and alkaline earth elements in some of the alteration zones. To help understand the origins of the mineral assemblages in altered Augustine rocks, we applied the thermochemical modeling program, GASWORKS, in calculations of: (a) reaction of the 1987 and 1989 gases with wall rock at 640 and 375??C; (b) cooling of the 1987 gas from 870 to 100??C with and without mineral fractionation; (c) cooling of the 1989 gas from 757 to 100??C with and without mineral fractionation; and (d) mixing of the 1987 and 1989 gases with air. The 640??C gas-rock reaction produces an assemblage consisting of silicates (tridymite, albite, diopside, sanidine and andalusite), oxides (magnetite and hercynite) and sulfides (bornite, chalcocite, molybdenite and sphalerite). The 375??C gas-rock reaction produces dominantly silicates (quartz, albite, andalusite, microcline, cordierite, anorthite and tremolite) and subordinate amounts of sulfides (pyrite, chalcocite and wurtzite), oxides (magnetite

  4. El Granito Calasuya: un intrusivo alcalifeldespático postcolisional en el batolito de Sierra Norte-Ambargasta, Córdoba The Calasuya Granite: a postcollisional alkalifeldspar intrusive in the Sierra Norte-Ambargasta batholith, Córdoba province

    Directory of Open Access Journals (Sweden)

    Javier Elortegui Palacios


    Full Text Available La zona central del extenso batolito Sierra Norte-Ambargasta, en el bloque más oriental de las Sierras Pampeanas orientales, está representada por granitoides de arco magmático tipo I (granodioritas, monzogranitos, pórfidos dacíticos y riolíticos denominados serie La Isla - Cerro de los Burros, intruidos por cuerpos menores félsicos postcolisionales, químicamente más evolucionados (denominados unidades Puesto de Los Caminos y Cerro Baritina, todos pertenecientes al Neoproterozoico- Cámbrico inferior. Nueva información geológica y geoquímica de la región centro-oriental del mismo batolito permitió identificar un plutón de composición alcalifeldespática, denominado Granito Calasuya, el primero de esta naturaleza en el batolito. Su mineralogía distintiva la constituyen la composición albítica de la plagioclasa magmática (An The central-western portion of the extended Sierra Norte-Ambargasta batholith, in the easternmost block of the eastern Sierras Pampeanas, is largely characterized by pre-collisional I-type magmatic arc granitoids (granodiorites, monzogranites, dacite and rhyolite porphyries named La Isla - Cerro de los Burros series, and by smaller sized postcollisional felsic intrusives of higher evolved chemistry (named Puesto de los Caminos and Cerro Baritina units, all of which crystallized along the Late Proterozoic -Lower Cambrian time span. New geological and geochemical data from the central and oriental areas of the batholith allowed to identify an intrusive body of alkalifeldspar composition (the Calasuya granite, the first of its type in the batholith. Its distinctive mineralogy is highlighted by the albitic composition of magmatic plagioclase (molar An < 6 %, the high #Fe (0.97 of accessory biotite, the presence of accessory late magmatic fluorite, and the conspicuous postmagmatic albitization process. Its highly fractionated nature is shown by high SiO2 and low CaO, MgO, TiO2, MnO and Fe2O3(t contents, also


    Institute of Scientific and Technical Information of China (English)

    张鹏辉; 张金亮; 董紫睿; 李德勇; 任伟伟; 罗忠琴


    Upper Cretaceous sandstones in the middle of Changling Depression of Songliao Basin mainly belong to lithic arkose, which experienced mechanical compaction,carbonate cementation, clay mineral cementation, silicate cementation, silicic cementation, dissolution of unstable components and local metasomatism. A variety of pore types in studied region include intergranular pores,intragranular pores,moldic pores,as well as a negligible amount of micro-pores and oversized pores. Among the pores,the intergranular pores are dominant. Two stages of oil inclusions in the Hua 5 (the first Member of Nenjiang Formation) were recognized. Hydrocarbon injection of the first period has low maturity,while the second B period possesses little hydrocarbon injection. Based on the diagenetic events, the diagenetic stages of the studied area are diversified from the early eodiagenesis B to the mesodiagenesis B,with the principal diagenetic stage being the mesodi-agenesis A. The classification of diagenetic facies in the area is discussed on the basis of sedimentary facies and diagenesis. Diagenetic facies can be classified into five types: they are compaction diagenetic facies, carbonate-cementation facies, unstable components dissolution facies, siliceous cementation facies and albite diagenetic facies. The unstable components dissolution facies and al-bite diagenetic facies constitute the favorable diagenetic facies in the studied region.%松辽盆地长岭凹陷中部上白垩统储层砂岩主要类型为岩屑长石砂岩,经历的成岩作用主要有以机械压实为主的压实作用,碳酸盐、粘土矿物、硅酸盐及硅质胶结为主的胶结作用,以长石、岩屑等不稳定组分溶解为主的溶蚀作用和局部发育的交代作用.研究区储层孔隙类型以粒间孔隙、粒内溶孔和铸模孔为主,其中粒间孔隙最为发育.储层砂岩成岩演化阶段处于早成岩B期—中成岩B期,主要为中成岩A期.结合沉积相和成岩作用特征,

  6. Tectonophysics of hydrothermal ore formation: an example of the Antei Mo-U deposit, Transbaikalia (United States)

    Petrov, V. A.; Rebetsky, Yu. L.; Poluektov, V. V.; Burmistrov, A. A.


    The Antei deposit of the southeastern Transbaikalian region is one of the largest uranium mines in Russia. It is hosted by the Late Paleozoic granitic basement of the Streltsovskaya caldera and was formed as a result of Late Mesozoic tectonothermal activity. Vein and stockwork-disseminated molybdenum-uranium mineralization at this deposit is controlled by zones of intense hydrothermal alteration, cataclasis, brecciation, and intense fracturing along steeply dipping faults, which acted as conduits for mineralizing fluids and hosts to the ore bodies. The upper edge of the ore-bearing zone is located at a depth of 400 m, and its lower edge was intersected at a depth of 1300 m from the day surface. The conditions of ore localization were determined using structural-geological and petrophysical studies coupled with numerical modeling of the effects of gravitational body forces at purely elastic and postcritical elastoplastic deformational stages. The dynamics of the tectonic stress field in the rock massif was reconstructed using the results of mapping of morphogenetic and kinematic characteristics of fault and fracture systems, as well as data on petrography and mineralogy of rocks and vein-filling material. It was shown that the fault framework of the deposit was formed in four tectonic stages, three of which took place in the geologic past and one of which reflects recent geologic history. Each tectonic stage was characterized by different parameters of the tectonic stress-strain field, fault kinematics, and conditions of mineral formation. The following types of metasomatic rocks are recognized within the deposit: high-temperature K-feldspar rocks and albitites (formed during the Late Paleozoic as the primary structural elements of a granitic massif) and Late Mesozoic low-temperature preore (hydromicatized rocks), synore (hematite, albite, chlorite, and quartz) and postore (kaolinite-smectite) rocks. The following petrophysical parameters were determined for all

  7. Lower Greenschist Facies Oscillations Across the Brittle-Ductile Transition Induced by Alternating Reaction Softening and Hardening Events (United States)

    Wintsch, R. P.; Yeh, M.


    Reaction textures associated with multiple fabrics in the Red River shear zone show evidence for both brittle and ductile deformation. Rocks on the eastern flank of the shear zone in the Diancang Shan block near Dali, Yunnan Province, China are dominated by porphyritic granodiorites and form the protoliths of the Red River fault rocks. The earliest fault-rocks are cataclasites in which fracture processes broke matrix feldspar grains. Grain-scale brittle fractures and crushed grains are well preserved in the >cm size relic K-feldspar phenocrysts, where multiple fractures are filled with newly precipitated quartz. Progressive deformation has displaced broken K-feldspar fragments into the evolving matrix establishing a cataclastic texture with abundant feldspar porphyroclasts. Ductile deformation is manifest in multiple generations of fabrics that wrap around these broken phenocrysts. The fabrics are defined primarily by muscovite and chlorite that form folia that may exceed the length of a thin section (several cm). Truncations and embayments of these minerals show that earlier magmatic feldspars and biotites have been dissolved and muscovite + chlorite + quartz have crystallized as reaction products. Reaction softening is clearly manifest by the replacement of K-feldspar and the crystallization of quartz as ribbons and muscovite in well aligned folia that define the mylonitic foliation. In some microstructural sites K-feldspar porphyroclasts themselves are truncated and engulfed by muscovite alone. These relationships suggest the simultaneous operation of the locally metasomatic ionic replacement reactions: K-feldspar + Na+ = Albite + K+ , and ΔV = -10% 3K-feldspar + 2H+ = muscovite + 6 quartz + 2K+ and ΔV = -16% 3Albite + K+ + 2H+ = muscovite + 6 quartz + 3Na+. ΔV = - 8% The latter two reactions produce muscovite and quartz, both much weaker than the reactant K-feldspar; these reactions constitute reaction softening. Moreover, the muscovite tends to align in

  8. ⁵³Mn-⁵³Cr and ²⁶Al-²⁶Mg ages of a feldspathic lithology in polymict ureilites

    Energy Technology Data Exchange (ETDEWEB)

    Goodrich, Cyrena Anne [Planetary Science Institute. Tucson, AZ (United States); Hutcheon, Ian D. [Glenn T. Seaborg Institute. Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Kita, Noriko T. [Dept. of Geoscience. Univ. of Wisconsin, Madison, WI (United States); Huss, Gary R. [NASA Marshall Space Flight Center (MSFC), Huntsville, AL (United States); Cohen, Barbara Anne [Hawaii Institute of Geophysics and Planetology. Univ. of Hawaii, Honolulu, HI (United States); Keil, Klaus


    We report 53Mn–53Cr and 26Al–26Mg isotopic data, obtained by in-situ SIMS analysis, for feldspathic clasts in polymict ureilites DaG 319 and DaG 165. The analyzed clasts belong to the “albitic lithology,” the most abundant population of indigenous feldspathic materials in polymict ureilites, and are highly fractionated igneous assemblages of albitic plagioclase, Fe-rich pyroxenes, phosphates, ilmenite, silica, and Fe(Mn, K, P, Ti)-enriched glass. Glass in DaG 165 clast 19 has extremely high and variable 55Mn/52Cr ratios (500–58,000) and shows correlated 53Cr excesses up to ~ 1500‰, clearly indicating the presence of live 53Mn at the time of formation. The slope of the well-correlated isochron defined by glass and pyroxenes from this clast corresponds to (53Mn/55Mn) = (2.84 ± 0.10) × 10-6 (2σ). Data for less 55Mn/52Cr-enriched glasses from DaG 319 clast B1, as well as phosphates from several other clasts, are consistent with this isochron. The 53Mn/55Mn ratio obtained from the isochron implies that these clasts are 0.70 ± 0.18 Ma younger than the D'Orbigny angrite, corresponding to the absolute age of 4563.72 ± 0.22 Ma. Plagioclase in DaG 319 clast B1 has a fairly constant 27Al/24Mg ratio of ~ 900 and shows resolvable 26Mg excesses of ~ 2‰. The slope of the isochron defined by pyroxene and plagioclase in this clast is (3.0 ± 1.1) × 10-7 (2σ), corresponding to a time difference of 5.4 (-0.3/+0.5) Ma after CAI (assuming the canonical initial 26Al/27Al ratio of 5 × 10-5) and an age 0.5 (-0.3/+0.5) Ma younger than D'Orbigny. Its absolute age (relative to D'Orbigny) is 4563.9 (+ 0.4/-0.5) Ma, in agreement with the 53Mn–53Cr age from clast 19. These data provide the first

  9. 松辽盆地南部HX井上白垩统青山口组黑色泥岩的矿物组成与自生微晶石英成因%Mineral Composition and Origin of Authigenic Quartz Crystals in Black Mudstone, in well HX, Qingshankou Formation, Upper Cretaceous, Songliao Basin

    Institute of Scientific and Technical Information of China (English)

    刘立; 王力娟; 杨永智; 于志超


    The mineral composition and diagenesis of shale play important roles in constraining the sealing efficiency as caprock of CO2 sequestration and the fracability in shale gas. X-ray fluorescence spectrum, X-ray diffraction and scanning electron microscopy are employed in the determination of mineral composition of mudstone and the identification of submicron-sized authigenic quartz crystals in well HX, Qingshankou Formation, Upper Cretaceous. The type of host rock and weathering effect are in consistent with mudstone in Qingshankou Formation. The mudstone is composed of clay mineral, albite, quartz and less K-feldspar. The clay fraction consists mainly of mixed-layer I/S and minor amounts of chlorite. Brittle mineral (albite, quartz and feldspar) average content is 44. 43%, and clay mineral content is 54. 26% on average. Submicron-sized authigenic quartz crystals released from S - I relation occur as large amounts of extremely fine-grained micro-sized crystals embedded as discrete,small clusters/nest and locate in micropores in mixed-layer I/S. The caprock consisting of mainly mixed-layer I/S mineral and minor amount of micron-quartz will be conductive to long-term CO2 geological storage. The content of brittle mineral meet the reservoir standard of industrial value shale gas, while the content of clay mineral is quite low.%泥质岩的矿物组成和成岩作用是制约其作为CO2地质封存的盖层封闭能力和作为页岩气储层具易压裂性质的重要原因.通过地球化学分析、X-射线衍射分析和扫描电镜观测及能谱测定,确定了松辽盆地南部HX井上白垩统青山口组泥岩的矿物组成.识别出了蒙皂石转变伊利石反应过程中形成的亚微米级自生微晶石英.研究表明:HX井上白垩统青山口组泥岩的母岩岩石类型和风化效应一致,泥岩主要由黏土矿物、钠长石和石英组成,钾长石少量;黏土矿物以伊利石/蒙皂石混层为主,其次为绿泥石;脆性矿物(钠

  10. Leaching kinetics in cyanide media of Ag contained in the industrial mining-metallurgical wastes in the state of Hidalgo, Mexico

    Institute of Scientific and Technical Information of China (English)

    Juan Hernandez⇑; Francisco Patino; Isauro Rivera; Iván Alejandro Reyes; Misrael Uriel Flores; Julio Cesar Juarez; Martín Reyes


    The leaching kinetics in cyanide media of the silver contained in the Dos Carlos waste tailings at the City of Pachuca de Soto, Hidalgo State, Mexico were carried out. The used material contained the following chemical composition: 56 ? 10-6 of Ag, 0.6 ? 10?6 of Au and 70.43% (by weight) of SiO2; 7.032% (by weight) of Al2O3; 2.69% (by weight) of Fe; 0.46% (by weight) of Mn; 3.98% (by weight) of K2O; 3.34%(by weight) of CaO;2.50% (by weight) of Na2O;0.04% (by weight) of Zn;0.026%(by weight) of Pb. The mineralogical phases present were the following:Silica, albite, argentite, berlinite, orthoclase, potassium jarosite, and natrojarosite. In the leaching kinetics in cyanide media, and under the studied conditions, the effect of the CN? concentration on the reaction rate has no effect on the whole process of alkaline cyanidation, of which the reaction order is n ? 0. Temperature has an effect on the cyanidation rate of the reaction, with an activation energy of 47.9 KJ/mol. At the same time, when the particle size decreases there is an increase in the reaction rate, which is inversely proportional to the particle diameter;when increasing the NaOH concentration there is an increase in the reaction rate Kexp, with a reaction order (n) of 0.215 under the studied ranges.

  11. 深处岩浆分异与某地花岗伟晶岩的形成

    Institute of Scientific and Technical Information of China (English)



    Two stages of intrusion have been recognized for Paleozoic pegmatites in this district. The pegmatites occur as several thousands of dikes, with 84 per cent of them distributed within three “thickly concentrated areas”. Similar horizontal zoning, i.e.,from the parental granite outwards the pegmatites vary from type K through type Na to type Li, is observed within these “thickly concentrated areas”, which consist of pegmatites of different stages. Temporally, the pegmatites also evolve in the same sequence of types K-Na-Li, with a series of mineralized dikes produced during this process. The occurrence of this phenomenan is not accidental but a strong indication of deepseated magmatic differentiation. In nature, not all granitic magmatism can bring about pegatite emplacement,nor all the pegmatite dikes are of the same petrological character. These differences indicate that deep-seated magmatic differentiation must be controlled by some factors.It's development is believed to be dependent largely on the amounts of both parental and residual magmas and on the extent to which the pressure at their source region has been lowered by the intrusion of granite. The constant movement of the crust results in the continuous upward migration of differentiated magma, so as to promote the differentiation to a greater extent, thereby providing new source materials for subsequent intrusive activity. Such a continuous movement of opposites leads to the formation of a complete series of pegmatites, i.e., from biotite-microcline pegmatite to lepidolite-albite pegmatite, giving rise to the “thickly concentrated areas” as well as a series of mineralized veins.

  12. Age constraints on the hydrothermal history of the Prominent Hill iron oxide copper-gold deposit, South Australia (United States)

    Bowden, Bryan; Fraser, Geoff; Davidson, Garry J.; Meffre, Sebastien; Skirrow, Roger; Bull, Stuart; Thompson, Jay


    The Mesoproterozoic Prominent Hill iron-oxide copper-gold deposit lies on the fault-bound southern edge of the Mt Woods Domain, Gawler Craton, South Australia. Chalcocite-bornite-chalcopyrite ores occur in a hematitic breccia complex that has similarities to the Olympic Dam deposit, but were emplaced in a shallow water clastic-carbonate package overlying a thick andesite-dacite pile. The sequence has been overturned against the major, steep, east-west, Hangingwall Fault, beyond which lies the clastic to potentially evaporitic Blue Duck Metasediments. Immediately north of the deposit, these metasediments have been intruded by dacite porphyry and granitoid and metasomatised to form magnetite-calc-silicate skarn ± pyrite-chalcopyrite. The hematitic breccia complex is strongly sericitised and silicified, has a large sericite ± chlorite halo, and was intruded by dykes during and after sericitisation. This paper evaluates the age of sericite formation in the mineralised breccias and provides constraints on the timing of granitoid intrusion and skarn formation in the terrain adjoining the mineralisation. The breccia complex contains fragments of granitoid and porphyry that are found here to be part of the Gawler Range Volcanics/Hiltaba Suite magmatic event at 1600-1570 Ma. This indicates that some breccia formation post-dated granitoid intrusion. Monazite and apatite in Fe-P-REE-albite metasomatised granitoid, paragenetically linked with magnetite skarn formation north of the Hangingwall Fault, grew soon after granitoid intrusion, although the apatite experienced U-Pb-LREE loss during later fluid-mineral interaction; this accounts for its calculated age of 1544 ± 39 Ma. To the south of the fault, within the breccia, 40Ar-39Ar ages yield a minimum age of sericitisation (+Cu+Fe+REE) of dykes and volcanics of ˜1575 Ma, firmly placing Prominent Hill ore formation as part of the Gawler Range Volcanics/Hiltaba Suite magmatic event within the Olympic Cu-Au province of the

  13. A multiscale hydro-geochemical-mechanical approach to analyze faulted CO 2 reservoirs: Original Research Article: A multiscale hydro-geochemical-mechanical approach to analyze faulted CO 2 reservoirs

    Energy Technology Data Exchange (ETDEWEB)

    Nguyen, Ba Nghiep [Pacific Northwest National Laboratory, Richland WA USA; Hou, Zhangshuan [Pacific Northwest National Laboratory, Richland WA USA; Bacon, Diana H. [Pacific Northwest National Laboratory, Richland WA USA; White, Mark D. [Pacific Northwest National Laboratory, Richland WA USA


    This paper applies a multiscale hydro-geochemical-mechanical approach to analyze faulted CO2 reservoirs using the STOMP-CO2-R code that is coupled to the ABAQUS® finite element package. STOMP-CO2-R models the reactive transport of CO2 causing mineral volume fraction changes that are captured by an Eshelby-Mori-Tanka model implemented in ABAQUS®. A three-dimensional (3D) STOMP-CO2-R model for a reservoir containing an inclined fault was built to analyze a formation containing a reaction network with 5 minerals: albite, anorthite, calcite, kaolinite and quartz. A 3D finite element mesh that exactly maps the STOMP-CO2-R grid is developed for coupled hydro-geochemical-mechanical analyses. The model contains alternating sandstone and shale layers. The impact of reactive transport of CO2 on the geomechanical properties of reservoir rocks and seals are studied in terms of mineral composition changes that affect their geomechanical responses. Simulations assuming extensional and compressional stress regimes with and without coupled geochemistry are performed to study the stress regime effect on the risk of hydraulic fracture. The tendency for the fault to slip is examined in terms of stress regime, geomechanical and geochemical-mechanical effects as well as fault inclination. The results show that mineralogical changes due to long-term injection of CO2 reduce the permeability and elastic modulus of the reservoir, leading to increased risk of hydraulic fracture in the injection location and at the caprock seal immediately above the injection zone. Fault slip is not predicted to occur. However, fault inclination and stress regime have an important impact on the slip tendency factor.

  14. Research on the Characteristics of Thorium Minerals in the Julongan Deposit, Xiangshan Ore Field%相山矿田居隆庵矿床钍矿物特征研究

    Institute of Scientific and Technical Information of China (English)

    孟艳宁; 范洪海; 孙志富; 陈璋如


    居隆庵矿床是相山矿田中一个大型的铀一钍混合矿床.通过系统的镜下显微特征研究和电子探针分析,查明了主要钍矿物和含钍矿物的种类,分析了钍的赋存状态和蚀交特征.钍的赋存状态有独立钍矿物、类质同象替换铀矿物和类质同象存在于副矿物中.相关的矿化蚀交有碳酸盐化、钠长石化、绢云母化、黄铁矿化、绿泥石亿、水云母化和萤石化.本文还总结了钍(铀)矿物的赋存位置.%Julongan deposit is a large uranium-thorium deposit in the Xiangshan ore field. This study investigated the thorium and thorium-bearing minerals and summarized occurrences and mineral alterations of thorium using microscope and electron microprobe techniques. The results indicated that thorium has several occurrences in the deposit,including independent thorium minerals, isomorphic form existing in uranium minerals, and micro-isomophic form lying in accessory minerals, and that mineralized alterations related with thorium are carbonation, albitization,sericitization, pyritization, chlortization, hydromicazation, and fluoritization; occurrence positions of thorium (uranium) minerals are also generalized. The above results provide materials and references for further study of the thorium minerals and deposits.

  15. Luminescence characterization of a sodium rich feldspar

    Energy Technology Data Exchange (ETDEWEB)

    Correcher, V.; Sanchez M, L. [CIEMAT, Av. Complutense 22, 28040 Madrid (Spain); Garcia G, J. [MNCN-CSIC, c/ J. Gutierrez Abascal 2, Madrid 28006 (Spain); Rivera, T. [CICATA-IPN, Av. Legaria 694, 11500 Mexico D.F. (Mexico)


    This paper reports on the radioluminescence (RL) and thermoluminescence (TL) properties of a sodium rich feldspar ((Na,K)[AlSi{sub 3}O{sub 8}]) with a mean molecular composition of orthoclase (Or) and albite (Ab) of Or{sub 1}Ab{sub 99}. Despite the complexity of the luminescence signals of the sample, it is possible to determine six different emission bands at about 300, 380, 420, 460, 550 and 680 nm. The 300 nm emission can be associated to structural defects related to the recombination process in which the Na{sup +} ion diffusion-limited is involved. The UV-blue emission band at (i) 380 nm is characteristic of mineral phases containing SiO{sub 4} tetrahedral and could be related to intrinsic defects in the lattice, (ii) the 420 nm band could be associated to the presence of Cu (II) ions placed next to the hole traps or the recombination on a centre formed from a hole-oxygen atom adjacent to two Al atoms (Al-O-Al) and (iii) the 460 nm waveband could be due to the presence of Ti{sup 4+}. The green and red emissions are respectively associated to the presence of Mn{sup 2+} and Fe{sup 3+} ions. The ratio between the relative intensities, peaked at 290 (the more intense waveband) and 550 nm is about 10:1 in both TL and RL; this fact indicates that the efficiency of recombination centres does no changes regardless on the type of the process. (Author)

  16. Influence of spectral interferences on the results of quartz determination by infrared spectrometry

    Directory of Open Access Journals (Sweden)

    Aleksandra Maciejewska


    Full Text Available Background: Determination of quartz by Fourier transform infrared spectrometry (FTIR is not specific: the obtained results are influenced by matrix components, some of which cause spectral interference. The aim of the study was to evaluate the effect of dust components responsible for spectral interference with quartz on the results of its determinations, and to develop methods to minimize the effects of interferences. Material and Methods: Investigation of interferent effects were conducted using respirable dusts: quartz SRM 1878a, cristobalite SRM 1879a, synthetic amorphous silica (Zeosil and feldspar, albite and kaolinite. For the study 17 mixtures with quartz and interferents at concentrations from 10 to 90% were prepared. Determinations of quartz were carried out by the KBr disc method. Results: In mixtures of quartz with interferents, the results based on bands 798–779 cm–1 were overestimated by 10–55%, while those based on band 695 cm–1 were closer to the true content of quartz. It was found that the best methods able to decrease the impact of spectral interference are: scaled subtraction of IR spectra of feldspar or kaolinite analysed in nonashed samples, correction curve for kaolinite also investigated in nonashed samples with quartz-content calculation based on band 695 cm–1 in mixtures with cristobalite, amorphous silica or kaolinite in ashed samples. Conclusions: The study indicates the need to identify spectral interferences in dust when determining crystalline silica by FT-IR and to take actions to minimize their impact on the obtained results. Med Pr 2015;66(4:497–509

  17. Significance of "stretched" mineral inclusions for reconstructing P- T exhumation history (United States)

    Ashley, Kyle T.; Darling, Robert S.; Bodnar, Robert J.; Law, Richard D.


    Analysis of mineral inclusions in chemically and physically resistant hosts has proven to be valuable for reconstructing the P- T exhumation history of high-grade metamorphic rocks. The occurrence of cristobalite-bearing inclusions in garnets from Gore Mountain, New York, is unexpected because the peak metamorphic conditions reached are well removed (>600 °C too cold) from the stability field of this low-density silica polymorph that typically forms in high temperature volcanic environments. A previous study of samples from this area interpreted polymineralic inclusions consisting of cristobalite, albite and ilmenite as representing crystallized droplets of melt generated during a garnet-in reaction, followed by water loss from the inclusion to explain the reduction in inclusion pressure that drove the transformation of quartz to cristobalite. However, the recent discovery of monomineralic inclusions of cristobalite from the nearby Hooper Mine cannot be explained by this process. For these inclusions, we propose that the volume response to pressure and temperature changes during exhumation to Earth's surface resulted in large tensile stresses within the silica phase that would be sufficient to cause transformation to the low-density (low-pressure) form. Elastic modeling of other common inclusion-host systems suggests that this quartz-to-cristobalite example may not be a unique case. The aluminosilicate polymorph kyanite also has the capacity to retain tensile stresses if exhumed to Earth's surface after being trapped as an inclusion in plagioclase at P- T conditions within the kyanite stability field, with the stresses developed during exhumation sufficient to produce a transformation to andalusite. These results highlight the elastic environment that may arise during exhumation and provide a potential explanation of observed inclusions whose stability fields are well removed from P- T paths followed during exhumation.

  18. Integrating petrography, mineralogy and hydrochemistry to constrain the influence and distribution of groundwater contributions to baseflow in poorly productive aquifers: insights from Gortinlieve catchment, Co. Donegal, NW Ireland. (United States)

    Caulfield, John; Chelliah, Merlyn; Comte, Jean-Christophe; Cassidy, Rachel; Flynn, Raymond


    Identifying groundwater contributions to baseflow forms an essential part of surface water body characterisation. The Gortinlieve catchment (5 km(2)) comprises a headwater stream network of the Carrigans River, itself a tributary of the River Foyle, NW Ireland. The bedrock comprises poorly productive metasediments that are characterised by fracture porosity. We present the findings of a multi-disciplinary study that integrates new hydrochemical and mineralogical investigations with existing hydraulic, geophysical and structural data to identify the scales of groundwater flow and the nature of groundwater/bedrock interaction (chemical denudation). At the catchment scale, the development of deep weathering profiles is controlled by NE-SW regional scale fracture zones associated with mountain building during the Grampian orogeny. In-situ chemical denudation of mineral phases is controlled by micro- to meso-scale fractures related to Alpine compression during Palaeocene to Oligocene times. The alteration of primary muscovite, chlorite (clinochlore) and albite along the surfaces of these small-scale fractures has resulted in the precipitation of illite, montmorillonite and illite-montmorillonite clay admixtures. The interconnected but discontinuous nature of these small-scale structures highlights the role of larger scale faults and fissures in the supply and transportation of weathering solutions to/from the sites of mineral weathering. The dissolution of primarily mineral phases releases the major ions Mg, Ca and HCO3 that are shown to subsequently form the chemical makeup of groundwaters. Borehole groundwater and stream baseflow hydrochemical data are used to constrain the depths of groundwater flow pathways influencing the chemistry of surface waters throughout the stream profile. The results show that it is predominantly the lower part of the catchment, which receives inputs from catchment/regional scale groundwater flow, that is found to contribute to the

  19. Hydrothermal alteration of plagioclase and growth of secondary feldspar in the Hengill Volcanic Centre, SW Iceland (United States)

    Larsson, D.; Grönvold, K.; Oskarsson, N.; Gunnlaugsson, E.


    Dissolution of igneous feldspar and the formation and occurrence of secondary feldspar in tholeiitic basalts from the Hengill volcanic centre, in SW Iceland was studied by microprobe analysis of cuttings from two ca. 2000 m deep geothermal wells. Well NG-7 in Nesjavellir represents a geothermal system in a rift zone where the intensity of young, insignificantly altered intrusions increases with depth. Well KhG-1 in Kolviðarhóll represents the margin of a rift zone where the intensity of intrusives is lower and the intensity of alteration higher. This marginal well represents altered basaltic crust in an early retrograde state. The secondary plagioclase in both wells is mainly oligoclase, occurring in association with K-feldspar and chlorite±actinolite. The texture of this assemblage depends on the lithology and intensity of alteration. In Nesjavellir (NG-7) the composition of secondary albite-oligoclase is correlated with the host-rock composition. This connection is not apparent in more intensely altered samples from Kolviðarhóll (KhG-1). The influence of temperature on composition of secondary Na-feldspar is unclear in both wells although Ca is expected to increase with temperature. Any temperature dependence may be suppressed by the influence of rock composition in Nesjavellir and by retrograde conditions at Kolviðarhóll. The absence of clear compositional gradients between igneous plagioclase and secondary feldspar and between Na-feldspar and K-feldspar suggests that secondary feldspars formed by dissolution precipitation reactions.

  20. Oxygen-isotope exchange and mineral alteration in gabbros of the Lower Layered Series, Kap Edvard Holm Complex, East Greenland

    Energy Technology Data Exchange (ETDEWEB)

    Fehlhaber, K.; Bird, D.K. (Stanford Univ., CA (United States))


    Multiple intrusions of gabbros, mafic dikes, and syenites in the Kap Edvard Holm Complex gave rise to prolonged circulation of meteoric hydrothermal solutions and extreme isotope exchange and mineral alteration in the 3,600-m-thick Lower Layered Series gabbros. In the Lower Layered Series, {delta}{sup 18}O of plagioclase varies from +0.3{per thousand} to {minus}5.8{per thousand}, and it decreases with an increase in the volume of secondary talc, chlorite, and actinolite. In the same gabbros, pyroxenes have a more restricted range in {delta}{sup 18}O, from 5.0{per thousand} to 3.8{per thousand}, and values of {delta}{sup 18}O{sub pyroxene} are independent of the abundance of secondary minerals, which ranges from 14% to 30%. These relations indicate that large amounts of water continued to flow through the rocks at temperatures of < 500-600C, altering the gabbros to assemblages of talc + chlorite + actinolite {plus minus}epidote {plus minus}albite and causing significant oxygen-isotope exchange in plagioclase, but not in pyroxene. The extensive low-temperature secondary mineralization and {sup 18}O depletion of plagioclase in the Lower Layered Series are associated with the later emplacement of dikes and gabbros and syenites, which created new fracture systems and provided heat sources for hydrothermal fluid circulation. This produced subsolidus mineral alteration and isotope exchange in the Lower Layered Series that are distinct from those in the Skaergaard and Cuillin gabbros of the North Atlantic Tertiary province, but are similar to those observed in some oceanic gabbros.

  1. Emplacement kinematics of nepheline syenites from the Terrane Boundary Shear Zone of the Eastern Ghats Mobile Belt, west of Khariar, NW Orissa: Evidence from meso- and microstructures

    Indian Academy of Sciences (India)

    T K Biswal; Harish Ahuja; Himansu Sekhar Sahu


    Nepheline syenite plutons emplaced within the Terrane Boundary Shear Zone of the Eastern Ghats Mobile Belt west of Khariar in northwestern Orissa are marked by a well-developed magmatic fabric including magmatic foliation, mineral lineations, folds and S-C fabrics. The minerals in the plutons, namely microcline, orthoclase, albite, nepheline, hornblende, biotite and aegirine show, by and large, well-developed crystal faces and lack undulose extinction and dynamic recrystallization, suggesting a magmatic origin. The magmatic fabric of the plutons is concordant with a solid-state strain fabric of the surrounding mylonites that developed due to noncoaxial strain along the Terrane Boundary Shear Zone during thrusting of the Eastern Ghats Mobile Belt over the Bastar Craton. However, a small fraction of the minerals, more commonly from the periphery of the plutons, is overprinted by a solid state strain fabric similar to that of the host rock. This fabric is manifested by discrete shear fractures, along which the feldspars are deformed into ribbons, have undergone dynamic recrystallization and show undulose extinction and myrmekitic growth. The shear fractures and the magmatic foliations are mutually parallel to the C-fabric of the host mylonites. Coexistence of concordant solid state strain fabric and magmatic fabric has been interpreted as a transitional feature from magmatic state to subsolidus deformation of the plutons, while the nepheline syenite magma was solidifying from a crystal-melt mush state under a noncoaxial strain. This suggests the emplacement of the plutons synkinematic to thrusting along the Terrane Boundary Shear Zone. The isotopic data by earlier workers suggest emplacement of nepheline syenite at 1500 + 3/− 4Ma, lending support for thrusting of the mobile belt over the craton around that time.

  2. Geochemistry of lamprophyres associated with uranium mineralization, Southeastern Desert, Egypt

    Institute of Scientific and Technical Information of China (English)


    Two brecciated shear zones (NNW-SSE) are found crosscutting cataclastic rocks. The cataclastic rocks (3.0 km2) occupy the core of the granitic pluton and enclose a roof pendant of mafic-ultramafic rocks. The NNW-SSE-extending lamprophyre dykes vary in thickness from 0.5 m to 1 m and up to 800 m long, cutting the cataclastic rocks and are composed mainly of plagioclases, amphiboles, relics of pyroxenes and K-feldspar phenocrysts embedded in fine-grained groundmass. They are characterized as being peraluminous, calc-alkaline in composition (chemical trap) and enriched in calcite, sulfide and P2O5.The lamprophyres were affected by hydrothermal alteration (chlorite-carbonate alteration) while the cataclastic rocks were affected by diagenetic alteration (K-feldspar-albite alteration).Uranium mineralization is the product of hydrothermal events and has been investigated by X-ray diffraction (XRD) and environmental scanning electron microscopy (ESEM), involving primary uranium minerals (U3O8) and secondary uranium minerals (uranophane and beta-uranophane, kasolite, torbernite, autonite and meta-autonite) in addition to U-bearing minerals (astrocyanite, betafite and fergusonite).The presence of different mineral parageneses associated with clay minerals indicates that the lamprophyres were subjected to acidic and alkaline mineralizing solutions. Moreover, the U-Zr/U, U-Ce/U values show negative correlations, confirming U-enrichment in both cataclastic rocks and shear zones while the Th-eU/eTh, Th-Zr/Th and Th-Ce/Th values show negative correlations, indicating that the U-bearing solutions are rich in Th in the cataclastic rocks only.

  3. Incorporation of seawater into mid-ocean ridge lava flows during emplacement (United States)

    Soule, S. A.; Fornari, D. J.; Perfit, M.; Cann, J. R.; Montési, L.; Ridley, W. I.


    Mid-ocean ridge (MOR) lava flows erupted at ~2000-3500 m below sea level contain large, cm- to m-sized cavities close to the upper surfaces of the flows. Within these cavities, lava drips (similar to lava stalactites found in terrestrial lava tubes) hang from the base of the upper crust. In order for these features to form, the cavities must exist as vapor-filled open space under hydrostatic pressures up to 35 MPa, and must maintain near-magmatic temperatures to attain the observed morphology of the drips. We have examined numerous lobate and sheet lava crusts from the fast-spreading East Pacific Rise in order to constrain the nature of the vapor that filled the cavities beneath these crusts, the extent of the interaction between the vapor and the liquid lava, and the impact of the vapor phase on flow emplacement. On the inner surfaces of large vesicles and cavities within the flow are mineral phases that appear to have grown at the interface between the liquid lava and vapor. These mineral phases have compositions distinct from those found in the flow interior (e.g., pure albite and forsterite), and show mineral growth habits indicative of undercooling of the lava. Preliminary thermodynamic modeling of the gas-liquid-solid interaction suggests that vapor derived from heated seawater is capable of producing the observed mineral compositions. In addition, we have found that quenched glass adjacent to analyzed vesicles can be enriched in Cl by an order of magnitude over ambient glass within the same sample suggesting that local mass exchange between the seawater and the lava has occurred. Here we present results of these analyses and accompanying thermodynamic modeling that lead us to conclude that the vapor filling the cavities is derived directly from seawater. In addition, we present numerical models investigating mechanisms for seawater incorporation and its impact on flow emplacement.

  4. Estimation of Temperature, Pressure and Oxygen Fugacity of the Cal-Alkaline Basin-Type Granitoids in the Winneba Area, Ghana

    Directory of Open Access Journals (Sweden)

    Nyarko Saah Esther


    Full Text Available In Ghana, the granitoids rocks are in two different groups, thus the basin type granitoid and the belt type granitoids. These granitoids have been studied petrographycally mineralogically and geochemically, especially the belt-type granitoids since it is the major host of gold occurrences in Ghana, however there are little studies on the petrogenesis and emplacement conditions of this important rock. In this paper we present the lacking knowledge on the emplacement conditions (temperature, pressure and the oxygen fugacity of the basin-type granitoids in the winneba area of Ghana.The calc-alkaline basin-type granitoids in the Winneba area is composed of quartz+ plagioclase +potash feldspar+ alkali feldspar+ Biotite+ Hornblende +amphibole+ titanite. The plagioclase composition ranges from Ab58 An1.7 Or0.45 to Ab98 An41 Or41 and mainly in the field of albite and oligoclase. The amphiboles however have a compositional range of Mg/(Mg +Fe ranging from 0.52 to 0.62 and a Si content of 7.1 to 7.4 atom per formula unit (afu. Their end-member compositions in the classification diagram are controlled by Magnesio-Hornblend, tschermakitic-Hornblend, and tschemakite substitution types. Scanning Electron Microscope (SEM analyses of coexisting hornblende and plagioclase (hornblende-plagioclase thermometry, Al content in hornblende (aluminum-in-hornblende barometry and the assemblage titanite-magnetite-quartz were used to constrain the P, T and fO2 during the crystallization of the parent magmas. The estimated temperature indicated an average temperature of crystallization of 677ºC reflecting late crystallization from highly oxidized magma (log fO2 -20 bars.The rocks were emplaced at an average pressure of 2.2 kbars corresponding to approximately 8 km depth of below the crust.

  5. Spectroscopic Evidence for Uranium Bearing Precipitates in Vadose Zone Sediments at the Hanford 300-Area Site

    Energy Technology Data Exchange (ETDEWEB)

    Arai, Yuji [Clemson Univ., SC (United States); Marcus, Matthew A. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Tamura, Nobumichi [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Davis, James A. [United States Geological Survey, Menlo Park, CA (United States); Zachara, John M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)


    Uranium(U) solid-state speciation in vadose zone sediments collected beneath the former North Process Pond (NPP) in the 300-Area of the Hanford site (WA, USA) was investigated using multi-scale techniques. In 30-day batch experiments, only a small fraction of total U (~7.4%) was released to artificial groundwater solutions equilibrated with 1% pCO2. Synchrotron-based micro X-ray fluorescence spectroscopy analyses showed that U was distributed among at least two types of species: 1) U discrete grains associated with Cu, and 2) areas with intermediate U concentrations on grains and grain coatings. Metatorbernite (Cu[UO2]2[PO4]2•8H2O) and uranophane (Ca[UO2]2[SiO3(OH)]2•5H2O) at some U discrete grains, and muscovite at U intermediate concentration areas were identified in synchrotron-based micro X-ray diffraction. SEM/EDS analyses revealed 8-10 µm size metatorbernite particles that were embedded in C-, Al-, and Si-rich coatings on quartz and albite grains. In μ- and bulk-X-ray Absorption Structure (μ-XAS and XAS) spectroscopy analyses, the structure of metatorbernite with additional U-C and U-U coordination environments were consistently observed at U discrete grains with high U concentrations. The consistency of the μ- and bulk-XAS analyses suggests that metatorbernite may comprise a significant fraction of the total U in the sample. The entrapped, micron-sized metatorbernite particles in C, Al, and Si rich coatings, along with the more soluble precipitated uranyl carbonates and uranophane, likely control the long-term release of U to water associated with the vadose zone sediments.

  6. Hydrochemistry and geothermometrical modeling of low-temperature Panticosa geothermal system (Spain) (United States)

    Asta, Maria P.; Gimeno, Maria J.; Auqué, Luis F.; Gómez, Javier; Acero, Patricia; Lapuente, Pilar


    The chemical characteristics of the low-temperature geothermal system of Panticosa (Spain) were investigated in order to determine the water temperature at the reservoir and to identify the main geochemical processes that affect the water composition during the ascent of the thermal waters. In general, the studied waters are similar to other geothermal systems in the Pyrenees, belonging to the group of granite-related alkaline thermal waters (high pH, low total dissolved solids, very low magnesium concentration, and sodium as the dominant cation). According to the alkaline pH of these waters, they have a very low CO2 partial pressure, bicarbonate is the dominant anion and silica is partially ionized as H3SiO4-. The unusually active acid-base pairs (HCO3-/CO32 - and, mainly, H4SiO4/H3SiO4-) act as homogeneous pH buffers and contribute to the total alkalinity in these alkaline waters. On the basis of the study of the conservative elements, a mixing process between a hot and a cold end-member has been identified. Additionally, in order to determinate the water temperature at the reservoir, several geothermometric techniques have been applied, including both geothermometrical modeling and classical geothermometrical calculations. The geothermometrical modeling seems to indicate that thermal waters re-equilibrate with respect to calcite and kaolinite during their ascent to the surface. Modeling results suggest that these thermal waters would be in equilibrium with respect to albite, K-feldspar, quartz, calcite, kaolinite and zoisite at a similar temperature of 90 ± 20 °C in the reservoir, which is in good agreement with the results obtained by applying the classical geothermometers.

  7. Cancrinite from nepheline syenite (mariupolite) of the Oktiabrski massif, SE Ukraine, and its growth history (United States)

    Dumańska-Słowik, Magdalena; Pieczka, Adam; Heflik, Wiesław; Sikorska, Magdalena


    Secondary cancrinite, (Na5.88K< 0.01)∑ 5.88(Ca0.62 Fe0.01Mn0.01Zn< 0.01 Mg< 0.01)∑ 0.64[Si6.44Al 5.56O24](CO3)0.67(OH)0.26(F< 0.01,Cl< 0.01)·2.04H2O), was found as accessory component of mariupolite (albite-aegirine nepheline syenite) from the Oktiabrski massif in the Donbass (SE Ukraine). It probably crystallized from a subsolidus reaction involving nepheline (and sodalite?) and calcite dissolved in the aqueous-carbonic fluid at the maximum temperature of 930 °C, decreasing to hydrothermal conditions. It is depleted in sodium, calcium and carbon, what results in the occurrence of vacant positions at both cationic and anionic sites. Ca-deficient cancrinite crystallized from the same hydrothermal Si-undersaturated fluids enriched in the ions such as Na+, Ca2 +, Cl-, F-, HCO3-, which formed calcite, sodalite, natrolite and fluorite. It has dark-red CL colours with patchy zoning, what indicates the variable/diverse fluid composition during its formation. In the CL spectrum of cancrinite only one broad emission band at 410 nm is observed, which can be attributed to O* center (the recombination of a free electron with an O- hole center). The formation of secondary CO3-rich species, i.e. cancrinite and calcite in mariupolite suggests that redox conditions in the Oktiabrski massif were oxidizing at the postmagmatic stage.

  8. Fluid-rock reactions in an evaporitic melange, Permian Haselgebirge, Austrian Alps (United States)

    Spotl, C.; Longstaffe, F.J.; Ramseyer, K.; Kunk, M.J.; Wiesheu, R.


    Tectonically isolated blocks of carbonate rocks present within the anhydritic Haselgebirge melange of the Northern Calcareous Alps record a complex history of deformation and associated deep-burial diagenetic to very low-grade metamorphic reactions. Fluids were hot (up to ~ 250 ??C) and reducing brines charged with carbon dioxide. Individual carbonate outcrops within the melange record different regimes of brine-rock reactions, ranging from pervasive dolomite recrystallization to dedolomitization. Early diagenetic features in these carbonates were almost entirely obliterated. Matrix dolomite alteration was related to thermochemical sulphate reduction (TSR) recognized by the replacement of anhydrite by calcite + pyrite ?? native sulphur. Pyrite associated with TSR is coarsely crystalline and characterized by a small sulphur isotope fractionation relative to the precursor Permian anhydrite. Carbonates associated with TSR show low Fe/Mn ratios reflecting rapid reaction of ferrous iron during sulphide precipitation. As a result, TSR-related dolomite and calcite typically show bright Mn(II)-activated cathodoluminescence in contrast to the dull cathodoluminescence of many (ferroan) carbonate cements in other deep-burial settings. In addition to carbonates and sulphides, silicates formed closely related to TSR, including quartz, K-feldspar, albite and K-mica. 40Ar/39Ar analysis of authigenic K-feldspar yielded mostly disturbed step-heating spectra which suggest variable cooling through the argon retention interval for microcline during the Late Jurassic. This timing coincides with the recently recognized subduction and closure of the Meliata-Hallstatt ocean to the south of the Northern Calcareous Alps and strongly suggests that the observed deep-burial fluid-rock reactions were related to Jurassic deformation and melange formation of these Permian evaporites.

  9. Authigenic potassium feldspar: a tracer for the timing of palaeofluid flow in carbonate rocks, Northern Calcareous Alps, Austria (United States)

    Spotl, C.; Kunk, M.J.; Ramseyer, K.; Longstaffe, F.J.


    This paper is included in the Special Publication entitled 'Dating and duration of fluid flow and fluid-rock interaction', edited by J. Parnell. Feldspar is a common authigenic constituent in Permian carbonate rocks which occur as tectonically isolated blocks within the evaporitic Haselgebirge melange in the Northern Calcareous Alps (NCA). Coexisting with pyrite, anhydrite, (saddle) dolomite, magnesite, fluorite and calcite, K-feldspar and minor albite record an event of regionally extensive interaction of hot brines with carbonate rocks. Detailed petrographic, crystallographic and geochemical studies reveal a variability in crystal size and shape, Al-Si ordering, elemental and stable isotopic compositions of the K-feldspar, which is only partially consistent with the traditional view of authigenic feldspar as a well-ordered, compositionally pure mineral. 40Ar-39Ar step- heating measurements of authigenic potassium feldspar from several localities yield two age populations, an older one of 145-154 Ma, and a younger one of c.90-97 Ma. Most age spectra reflect cooling through the argon retention temperature interval, which was rapid in some localities (as indicated by plateau ages) and slower in others. Rb-Sr isotope data are more difficult to interpret, because in many K-feldspar samples they are controlled largely by Sr-bearing inclusions. The Jurassic 40Ar-39Ar dates are interpreted as minimum ages of feldspar growth and hence imply that fluid-rock interaction is likely to be simultaneous with or to slightly predate melange formation. Deformation associated with the closure and subduction of the Meliata-Hallstatt ocean south of the NCA during the Upper Jurassic is regarded as the principal geodynamic driving force for both enhanced fluid circulation and melange formation. Some localities were reheated beyond the argon retention temperature for microcline during mid-Cretaceous nappe stacking of the NCA, thus obliterating the older signal.

  10. Preliminary stratigraphic and petrologic characterization of core samples from USW-G1, Yucca Mountain, Nevada

    Energy Technology Data Exchange (ETDEWEB)

    Waters, A.C.; Carroll, P.R. (eds.)


    Tuffs of the Nevada Test Site are currently under investigation to determine their potential for long-term storage of radioactive waste. As part of this program, hole USW-G1 was drilled to a depth of 6000 ft below the surface, in the central part of the Yucca Mountain area, Nevada Test Site, Nevada. Petrographic study of the USW-G1 core is presented in this report and shows the tuffs (which generally were variably welded ash flows) are partly recrystallized to a variety of secondary minerals. The important alteration products are zeolites (heulandite, clinoptilolite, mordenite and analcime), smectite clays with minor interstratified illite, albite, micas, potassium feldspar, and various forms of silica. Iijima`s zeolite zones I through IV of burial metamorphism can be recognized in the core. Zeolites are first observed at about the 1300-ft depth, and the high-temperature boundary of zeolite stability in this core occurs at about 4350 ft. Analcime persists, either metastably or as a retrograde mineral, deeper in the core. The oxidation state of Fe-Ti oxide minerals, through most of the core, increases as the degree of welding decreases, but towards the bottom of the hole, reducing conditions generally prevail. Four stratigraphic units transected by the core may be potentially favorable sites for a waste repository. These four units, in order of increasing depth in the core, are (1) the lower cooling unit of the Topopah Spring Member, (2) cooling unit II of the Bullfrog Member, (3) the upper part of the Tram tuff, and (4) the Lithic-rich tuff.

  11. Trace elements and mineral composition of waste produced in the process of combustion of solid fuels in individual household furnaces in the Upper Silesian Industrial Region (Poland

    Directory of Open Access Journals (Sweden)

    Smołka-Danielowska Danuta


    Full Text Available This study presents preliminary research results, with regard to the concentration of chosen trace elements (Mn, Cr, Tl, Ni, Cu, Zn, As, Cd, Ba, Pb in waste, which was produced in the process of combustion of solid fuels (hard coal and flotation concentrate of bituminous coal in individual household furnaces in Poland (in the Upper Silesian Industrial Region. 27 samples of ash, 4 samples of hard coal and 2 samples of flotation concentrate of bituminous coal were prepared for the research. Methods such as: ICP-MS, X-ray diffraction by means of the powder method and scanning electron microscopy were used during the research. In the ash samples obtained from the combustion of hard coal, the highest average concentrations were: Mn (1477.7 ppm, Ba (1336.4 ppm and Zn (599.7 ppm. In the samples obtained from the combustion of flotation concentrate of bituminous coal, the highest average concentrations was stated for: Zn (762.4 ppm, Mn (668.5 ppm, Pb (552.1 ppm and Ba (211.7 ppm. Crystalline components were determined by used the X-ray diffraction method and the samples of ash obtained from the combustion of hard coal contained: anhydrite, gypsum, hematite, magnetite, quartz, calcite, mullite, periclase, kaolinite, dolomite, pyrite, sphalerite, galena and feldspars (albite-anorthite. The samples of ash obtained from the combustion of flotation concentrate of bituminous coal contain: pyrite, quartz, potassium feldspar, muscovite and kaolinite. The scanning electron microscope analysis enabled the identification of the chemical composition of single ash grains and determined their morphology (aluminosilicate forms, substance PbS and ZnS, oxides of Ni, Cu and Mn, monazite, xenotime.

  12. Advanced degradation of brominated epoxy resin and simultaneous transformation of glass fiber from waste printed circuit boards by improved supercritical water oxidation processes. (United States)

    Liu, Kang; Zhang, Zhiyuan; Zhang, Fu-Shen


    This work investigated various supercritical water oxidation (SCWO) systems, i.e. SCWO1 (only water), SCWO2 (water+H2O2) and SCWO3 (water+H2O2/NaOH), for waste printed circuit boards (PCBs) detoxification and recycling. Response surface methodology (RSM) was applied to optimize the operating conditions of the optimal SCWO3 systems. The optimal reaction conditions for debromination were found to be the NaOH of 0.21g, the H2O2 volume of 9.04mL, the time of 39.7min, maximum debromination efficiency of 95.14%. Variance analysis indicated that the factors influencing debromination efficiency was in the sequence of NaOH>H2O2>time. Mechanism studies indicated that the dissociated ions from NaOH in supercritical water promoted the debromination of brominated epoxy resins (BERs) through an elimination reaction and nucleophilic substitution. HO2, produced by H2O2 could induce the oxidation of phenol ring to open (intermediates of BERs), which were thoroughly degraded to form hydrocarbons, CO2, H2O and NaBr. In addition, the alkali-silica reaction between OH(-) and SiO2 induced the phase transformation of glass fibers, which were simultaneously converted into anorthite and albite. Waste PCBs in H2O2/NaOH improved SCWO system were fully degraded into useful products and simultaneously transformed into functional materials. These findings are helpful for efficient recycling of waste PCBs.

  13. Physicochemical Conditions of the Formation of Beryl and Aquamarin in Mufushan Granopegmatite Deposit,Hunan Province,China

    Institute of Scientific and Technical Information of China (English)

    李兆麟; 牛贺才; 等


    The formation of the Mufushan granopegmatite was closely related to the Late Yenshanian multiphase and multistage magmatic activities,More than one generation of beryl and aquamarine occur in different types of pegmatite in the granites.The presence of melt and melt-fluid inclusions strongly indicates a melt-solution character of the pegmatitic magma.Forming temperatures of the different generations of beryl in a Na+-K+,Ca2+-CO32--Cl--SO42- solution ranges from 990℃to 200℃.Aquamarine was formed at 720-180℃.The contents of alkali metals(Na++K+)in th ore-formming solution of aquamarine are lower than those in the beryl,but the contents of alkali earths(Ca) and salinity are higher,The granite was generated by remelting of the basement formation(meta-sedimentary rocks of the Lengjiaxi Group)which also served as the source of ore-forming material.Beryllium in the pegmatite was transported mainly in the form of Na[Be(CO3)2],with part of it being complexed with Cl- and SO42-.During the generation and evolution of the pegmatite,equilibrium might have been reached in the solid-melt-fluid or solid-fluid system.The intergranular solutions may have reacted with the early crystallized minerals,resulting in potash-feldsparization,albitization and muscovitization during which the ore-forming elements were mobilized and transported in favour of ore deposition.

  14. Influence of ash composition on the sintering behavior during pressurized combustion and gasification process

    Institute of Scientific and Technical Information of China (English)

    Ni-jie JING; Qin-hui WANG; Yu-kun YANG; Le-ming CHENG; Zhong-yang LUO; Ke-fa CEN


    To determine the ash characteristics during fluidized bed combustion and gasification purposes,the investigation of the impacts of chemical composition of Jincheng coal ash on the sintering temperature was conducted.A series of experiments on the sintering behavior at 0.5 MPa was performed using the pressurized pressure-drop technique in the combustion and gasification atmospheres.Meanwhile,the mineral transformations of sintered ash pellets were observed using X-ray diffractometer (XRD) analyzer to better understand the experimental results.In addition,quantitative XRD and field emission scanning electron microscope/energy dispersive X-ray spectrometer (FE-SEM/EDS) analyses of ash samples were used for clarifying the detailed ash melting mechanism.These results show that the addition of Fe2O3 can obviously reduce the sintering temperatures under gasification atmospheres,and only affect a little the sintering temperature under combustion atmosphere.This may be due to the presence of iron-bearing minerals,which will react with other ash compositions to produce low-melting-point eutectics.The FE-SEM/EDS analyses of ash samples with Fe2O3 additive show consistent results with the XRD measurements.The CaO and Na2O can reduce the sintering temperatures under both the combustion and gasification atmospheres.This can be also contributed to the formation of low-melting-point eutectics,decreasing the sintering temperature.Moreover,the fluxing minerals,such as magnetite,anhydrite,muscovite,albite and nepheline,contribute mostly to the reduction of the sintering temperature while the feldspar minerals,such as anorthite,gehlenite and sanidine,can react with other minerals to produce low-melting-point eutectics,and thereby reduce the sintering temperatures.

  15. Geochemistry of metamorphosed basaltic and sedimentary rocks from the Smolník Cu-pyrite deposit (Gemeric Superunit, Western Carpathians: a reappraisal of older geochemical data

    Directory of Open Access Journals (Sweden)

    Peter Ivan


    Full Text Available Stratiform chalcopyrite-pyrite deposit of Smolník is located in the low-grade metamorphosed Early Palaeozoic volcano-sedimentary Gelnica Group. Various types of phyllites, mostly sericite and graphite-sericite phyllites with metadolerite bodies build up proximate vicinity of the deposit. The imminent host rocks of sulphide pods are chlorite phyllites with subordinate chlorite-sericite phyllites intercallations. Metadolerites previously interpreted as effusive rocks are probably subvolcanic in origin. Original igneous mineral association of clinopyroxene, plagioclase, ilmenite and probably also olivine were transformed to association of amphiboles, albite, clinozoisite/epidote, titanite ± calcite by metamorphic alteration. Composition of metadolerites is close to basaltic liquids although indices of some fractionation of plagioclase, olivine/chromspinelide or clinopyroxene exist. Trace element distribution points to their similarity to within-plate continental tholeiites (CT and probable relation to the beginning of rifting in the Lower Devonian time. Three possible sources of sedimentary material have been identified in the sedimentary host rocks of the Smolník deposit: (i basalts generated from enriched mantle reservoir; (ii less fractionated calc-alkaline volcanic rocks and (iii fractionated calc-alkaline rhyolites. An additional hydrothermal source for silica and iron is supposed for chlorite phyllites and allows classified them as metaexhalites. The sulphide ores were directly precipitated in the exhalite environment due to reaction hydrothermal solution with hydrogen sulphide produced by thermochemical reduction of the marine sulphate. Geochemical data on metamorphosed dolerites and sediments in combination to other geological characteristics of the Smolník deposit support its classification as the Besshi-type deposit.

  16. Chemical modifications accompanying blueschist facies metamorphism of Franciscan conglomerates, Diablo Range, California (United States)

    Moore, Diane E.; Liou, J.G.; King, B.-S.


    As part of an investigation of blueschist-facies mineral parageneses in pebbles and matrix of some Franciscan metaconglomerates of the Diablo Range, California, textural and major-element chemical analyses were conducted on a number of igneous pebbles that comprise a range of rock types from granite and dacite to gabbro and basalt. Compositions of the igneous pebbles differ significantly from common igneous rocks, particularly with respect to Ca, K, Na, Si and H2O. The SiO2 and H2O contents are characteristically high and the K2O contents low. The CaO and Na2O contents may be relatively enriched or reduced in different pebbles. The igneous pebbles show little evidence of alteration prior to their incorporation into the Franciscan conglomerates, and the chemical modifications are considered to have been produced during metamorphism of the conglomerates to (lawsonite + albite + aragonite ?? jadeite)-bearing assemblages. The observed variations in the pebbles are shown to be functions of: (1) bulk chemistry; (2) the igneous mineral assemblage; (3) the stable metamorphic mineral assemblage; and (4) the composition of pore fluids in the conglomerates. The relative proportions of Mg and Fe in most of the pebbles apparently have been unaffected by the metamorphism, and these parameters, along with other textural and chemical factors, were used to determine the petrogenetic affinities of the igneous pebbles. The plutonic and most of the volcanic pebbles correspond to calc-alkaline rock series, whereas a few volcanic pebbles show apparent Fe-enrichment characteristic of tholeiitic rocks. A continental margin arc-batholith complex would be the best source for these igneous detrital assemblages. Conglomerates in local areas differ in igneous lithologies from conglomerates in other areas and probably differ somewhat in age, perhaps reflecting varying degrees of unroofing of such a complex during deposition of Franciscan sediments. ?? 1981.

  17. Site investigation SFR. Fracture mineralogy and geochemistry of borehole sections sampled for groundwater chemistry and Eh. Results from boreholes KFR01, KFR08, KFR10, KFR19, KFR7A and KFR105

    Energy Technology Data Exchange (ETDEWEB)

    Sandstroem, Bjoern (WSP Sverige AB (Sweden)); Tullborg, Eva-Lena (Terralogica AB, Grabo (Sweden))


    This report is part of the complementary site investigations for the future expansion of SFR. The report presents the results obtained during a detailed mineralogical and geochemical study of fracture minerals in drill cores from borehole section sampled for groundwater chemistry and where downhole Eh measurements have been performed. The groundwater redox system comprises not only the water, but also the bedrock/fracture mineral system in contact with this water. It is thus important to gain knowledge of the solid phases in contact with the groundwater, i.e. the fracture minerals. The samples studied for mineralogy and geochemistry, here reported, were selected to represent the fracture surfaces in contact with the groundwater in the sampled borehole sections and will give input to the hydrogeochemical model (SFR SDM). The mineralogy was determined using SEM-EDS and XRD and the geochemistry of fracture filling material was analysed by ICP-AES and ICP-QMS. The most common fracture minerals in the samples are mixed layer clay (smectite-illite), illite, chlorite, calcite, quartz, adularia and albite. Other minerals identified in the borehole sections include laumontite, pyrite, barite, chalcopyrite, hematite, Fe-oxyhydroxide, muscovite, REE-carbonate, allanite, biotite, asphaltite, galena, sphalerite, arsenopyrite, uranium phosphate, uranium silicate, Y-Ca silicate, monazite, xenotime, harmotome and fluorite. There are no major differences between the fracture mineralogy of the investigated borehole sections from SFR and the fracture mineralogy of the Forsmark site investigation area. The four fracture mineral generations distinguished within the Forsmark site investigation are also found at SFR. However, some differences have been observed: 1) Barite and uranium minerals are more common in the SFR fractures, 2) clay minerals like mixed layer illite-smectite and illite dominates in contrast to Forsmark where corrensite is by far the most common clay mineral and, 3

  18. Subsolidus alkali metasomatism in the metamorphosed Ordovician acid volcanics and volcaniclastics of the Gelnica Group (Gemeric Superunit, Western Carpathians

    Directory of Open Access Journals (Sweden)

    Mária Šimurková


    Full Text Available The Early Paleozoic Gelnica Group (Gemeric Superunit, Western Carpathians is composed of low-grade metamorphosed flysch-like sedimentary complexes alternated with volcanogenic complexes built up mostly by acid volcaniclastic rocks. Volcaniclastic rocks and small rhyolite bodies Ordovician in age underwent subsolidus alkali metasomatism locally overprinted by multiple stages of younger metamorphic and hydrothermal alterations. The observed variability in chemical compositions indicates that the most of acid volcanic and volcaniclastic rocks experienced potassic or sodium metasomatic alteration, the unaltered or Mg-metasomatised rocks occur less frequently. The dominating K-metasomatism is related mainly to the K-feldspar, partly also biotite and muscovite/sericite formation at the expense of matrix or original feldspar phenocrysts. The Na-metasomatism is connected with albite formation. The highest concentrations of alkalies (up to 13.52 wt. % K2O and 7.08 wt. % Na2O respectively have been found in rocks originally represented by glassy dacites. The elements like Al, Ti and Zr remain immobile in alkaline metasomatic processes in contrast to Rb or metals. Based on the results from areas with analogical geological structure and evolution, especially the Bergslagen area in Sweden, we suppose that alkali metasomatism in the Gelnica Group is a product of hydrothermal system caused by the infiltration and circulation of sea water. The areas with K-, Na- or Mg-metasomatism represent different parts of the original hydrothermal system, where the K-metasomatism was probably its lower temperature section. This hydrothermal system probably mobilised some metals (Cu, Pb, Zn, Fe, Mn for the formation of stratiform sulfide and oxide mineralizations or served as the metal pre-concentrator for younger siderite-sulfide vein deposits.

  19. Physicochemical impacts of dust particles on alpine glacier meltwater at the Laohugou Glacier basin in western Qilian Mountains, China. (United States)

    Dong, Zhiwen; Qin, Dahe; Chen, Jizu; Qin, Xiang; Ren, Jiawen; Cui, Xiaoqing; Du, Zhiheng; Kang, Shichang


    This work discusses the temporal variation of various physicochemical species in the meltwater runoff of Laohugou Glacier No. 12 (4260 ma.s.l.) in central Asia, and their correlation with dust particles, based on a two-year field observation in summer 2012 and 2013, mainly focusing on dust concentration and size distribution, meltwater chemistry, particles SEM-EDX analysis in the meltwater, and MODIS atmospheric optical depth fields around the Qilian Mountains in central Asia. We find that, the volume-size distribution of dust particles in the meltwater is mainly composed of three parts, which includes fine aerosol particles (with diameter of 0~3.0 μm, mainly PM 2.5), atmospheric dust (with diameter of 3.0~20 μm), and local dust particles (20~100 μm), respectively. Comparison of dust particles in the snowpack and meltwater runoff indicates that, large part of dust particles in the meltwater may have originated from atmospheric dust deposition to the snow and ice on the glacier, and transported into the meltwater runoff. Moreover, temporal variation of dust and major ions (especially crustal species) is very similar with each other, showing great influence of dust particles to the chemical constituents of the glacier meltwater. SPM and TDS implied significant influences of dust to the physical characteristics of the glacier meltwater. Results showed that, accelerated glacier melting may affect physicochemical characteristics of the meltwater at an alpine basin under global warming. MODIS atmospheric optical depth (AOD) fields derived using the Deep Blue algorithm, showed great influence of regional dust transportation over western Qilian Mountains in springtime. SEM-EDX analysis shows that dust particles in the glacier meltwater contain Si-, Al-, Ca-, K-, and Fe-rich materials, such as quartz, albite, aluminate, and fly ash, similar to that deposited in snowpack. These results showed great and even currently underestimated influences of atmospheric dust

  20. Petrography and geochemical study of Nezam-Abad area, Southwest of Shazand, Arak

    Directory of Open Access Journals (Sweden)

    Robabeh Jafari


    Full Text Available Nezam-Abad area is located in southwest of Shazand (Arak which is a part of Sanandaj-Sirjan zone. Major intrusive rocks of Nezam-Abad are quartz diorite and minor amount of granodiorite. Leucogranitic, pegmatite dykes and quartz-tourmaline veins were intruded the quartz diorite. Quartz diorites are mainly composed of plagioclase, hornblende, biotite, quartz and pyroxene as major minerals. Major minerals of leucogranite are microcline, orthoclase, albite, quartz, biotite and muscovite. Accessory minerals consist of apatite, zircon, sphene, epidote, allanite, tourmaline and opaque. The presence of hydrous minerals like hornblende and biotite in these rocks indicate that the corresponding magma initially contained >3 wt% H2O (wet magma. The occurrences of garnet and andalusite minerals suggest assimilation process. Primary textures in these rocks are granular, granophyre, and poikilitic. Secondary textures are perthite, myrmekite, sericitization, chloritization and kaolinitization. Later hydrothermal activities and tectonic strains are factors for presence of perthite texture in leucogranite. K amount for sericitization of feldspars come from the K-feldspars and chloritization of biotite. Transformation of biotite to muscovite indicates the act of K rich fluid in later stages. On the basis of chemical analysis on the intrusive rocks, it is shown that the magma was calc-alkaline, metaluminous-peraluminous and medium-K to high-K. Study of major elements in Harker diagrams indicates Al2O3, FeO, Fe2O3 and CaO decrease with increasing of SiO2 and K2O and Na2O increase indicating that fractional crystallization may have played an important role in the formation of granitoid rocks from Nezam-Abad.

  1. Effect of petrophysical properties and deformation on vertical zoning of metasomatic rocks in U-bearing volcanic structures: A case of the Strel'tsovka caldera, Transbaikal region (United States)

    Petrov, V. A.; Andreeva, O. V.; Poluektov, V. V.


    The development of vertical zoning of wall-rock metasomatic alteration is considered with the Mesozoic Strel'tsovka caldera as an example. This caldera hosts Russia's largest uranium ore field. Metasomatic rocks with the participation of various phyllosilicates, carbonates, albite, and zeolites are widespread in the ore field. In the eastern block of the caldera, where the main uranium reserves are accommodated, hydromica metasomatic alteration gives way to beresitization with depth. Argillic alteration, which is typical of the western block, is replaced with hydromica and beresite alteration only at a significant depth. Postore argillic alteration is superposed on beresitized rocks in the lower part of the section. Two styles of vertical metasomatic zoning are caused by different modes of deformation in the western and eastern parts of the caldera. Variations of the most important petrophysical properties of host rocks—density, apparent porosity, velocities of P- and S-waves, dynamic Young's modulus, and Poisson coefficient—have been determined by sonic testing of samples taken from different depths. It is suggested that downward migration of the brittle-ductile transition zone could have been a factor controlling facies diversity of metasomatic rocks. Such a migration was caused by a new phase of tectonothermal impact accompanied by an increase in the strain rate or by emplacement of a new portion of heated fluid. Transient subsidence of the brittle-ductile boundary increases the depth of the hydrodynamically open zone related to the Earth's surface and accelerates percolation of cold meteoric water to a greater depth. As a result, the temperature of the hydrothermal solution falls down, increasing the vertical extent of argillic alteration. High-grade uranium mineralization is also localized more deeply than elsewhere.

  2. Microtectonic-assisted P-T determination on low-grade Alpine metamorphic rocks from the "Tisia Mega-Unit" of the Slavonian Mountains in Croatia (United States)

    Balen, Dražen; Lihter, Iva; Massonne, Hans-Joachim


    The internal structure of the Tisia (Tisza) Mega-Unit in the Alpine-Carpathian-Dinaridic orogenic system encompasses large Alpine nappe systems brought to its present-day position by complex regional-scale movements. The Slavonian Mountains are part of the Bihor nappe system which is below the Codru and above the Mecsek nappe systems. The low-grade metamorphic schist unit of the Slavonian Mountains includes numerous rocks which were previously related to Precambrian and/or Lower Paleozoic orogeneses. However, recent studies (e.g. Balen, 2014, European Geosciences Union General Assembly, EGU 2014-6122) show that the metapelites of this unit should be attributed to the Alpine orogeny and the poorly known P-T conditions, which they experienced, should be refined. Although metapelites can be sensitive to changes of metamorphic conditions and, therefore, be suitable for the P-T estimation of metamorphic event(s), the extraction of mineral assemblages, being in equilibrium, and associated microtectonic data for particular low-grade metamorphic rocks is not straightforward. On the contrary, due to lack of suitable minerals and complex mictotectonic features, one can be faced with a severe problem concerning (dis)equilibrium. To avoid this, the observation scale in the research was set to the sub-mm level taking into account microtectonic positions of minerals. The investigated samples from the Slavonian Mountains are fine-grained schists consisting of chlorite (15-30 vol. %), white mica (15-25 vol. %), quartz (10-25 vol. %), feldspars (albite 10-15 vol. %; some K-feldspar), biotite (ages (113±20 and 82±23 Ma; Balen, 2014) has a significance in clarifying details of the geodynamic evolution during the Alpine orogeny. Financial support by the Croatian Science Foundation (IP-2014-09-9541) and T. Theye's help during microprobe work is greatly acknowledged.

  3. Biochemical distributions (amino acids, neutral sugars, and lignin phenols) among size-classes of modern marine sediments from the Washington coast (United States)

    Keil, Richard G.; Tsamakis, Elizabeth; Giddings, J. Calvin; Hedges, John I.


    In order to examine relationships of organic matter source, composition, and diagenesis with particle size and mineralogy in modern marine depositional regimes, sediments from the continental shelf and slope along the Northwest Pacific rim (Washington coast, USA) were sorted into hydrodynamic size fractions (sand: >250, 63-250 μm; silt: 35-63, 17-35, 8-17, 3-8 μm; and clay-sized: 1-3, 0.5-1, fucose and rhamnose. Organic matter in the silt fractions, though degraded, is not as diagenetically altered as in the clay fractions. Enrichment of pollen grains in the silt-size material is reflected by high cinnamic acid to ferulic acid lignin phenol ratios. The highest pollen biochemical signal is observed in the silt fractions of the deepest station (1835 m), where pollen abundances are also highest. Organic matter tightly bound in the silt and sand-sized fractions are enriched in aldoses and show indications of enhanced microbial biomass as reflected by high weight percentages of ribose. Distinct organic debris was composed of relatively unaltered vascular plant remains as reflected by high lignin phenol yields and low acid/aldehyde ratios. Clay-size fractions are enriched in nitrogenous components, as reflected by elevated yields of total and basic amino acids (especially lysine). Silt- and sand-size fractions rich in quartz and albite show slightly higher yields of neutral amino acids. Consistent trends across all size classes and among the different depositional settings illustrates that only a small portion of the organic matter is present as distinct organic debris (e.g. pollen, vascular plant tissues, etc.), but that this debris can be isolated in specific size classes. The data for surface-associated organic matter are consistent with, but not conclusive of, selective partitioning of some organic matter to specific mineral surfaces. The dominant size class-specific trends in organic matter composition are due to changes in both source and diagenetic alteration.

  4. Fundamental study of CO2-H2O-mineral interactions for carbon sequestration, with emphasis on the nature of the supercritical fluid-mineral interface.

    Energy Technology Data Exchange (ETDEWEB)

    Bryan, Charles R.; Dewers, Thomas A.; Heath, Jason E.; Wang, Yifeng; Matteo, Edward N.; Meserole, Stephen P.; Tallant, David Robert


    In the supercritical CO2-water-mineral systems relevant to subsurface CO2 sequestration, interfacial processes at the supercritical fluid-mineral interface will strongly affect core- and reservoir-scale hydrologic properties. Experimental and theoretical studies have shown that water films will form on mineral surfaces in supercritical CO2, but will be thinner than those that form in vadose zone environments at any given matric potential. The theoretical model presented here allows assessment of water saturation as a function of matric potential, a critical step for evaluating relative permeabilities the CO2 sequestration environment. The experimental water adsorption studies, using Quartz Crystal Microbalance and Fourier Transform Infrared Spectroscopy methods, confirm the major conclusions of the adsorption/condensation model. Additional data provided by the FTIR study is that CO2 intercalation into clays, if it occurs, does not involve carbonate or bicarbonate formation, or significant restriction of CO2 mobility. We have shown that the water film that forms in supercritical CO2 is reactive with common rock-forming minerals, including albite, orthoclase, labradorite, and muscovite. The experimental data indicate that reactivity is a function of water film thickness; at an activity of water of 0.9, the greatest extent of reaction in scCO2 occurred in areas (step edges, surface pits) where capillary condensation thickened the water films. This suggests that dissolution/precipitation reactions may occur preferentially in small pores and pore throats, where it may have a disproportionately large effect on rock hydrologic properties. Finally, a theoretical model is presented here that describes the formation and movement of CO2 ganglia in porous media, allowing assessment of the effect of pore size and structural heterogeneity on capillary trapping efficiency. The model results also suggest possible engineering approaches for optimizing trapping capacity and for

  5. Geochemical characteristics of pyrite in Duolanasayi gold deposit, Xinjiang

    Institute of Scientific and Technical Information of China (English)

    CHEN Guodong; XIAO Huiliang; WANG Henian; ZHOU Jiyuan


    The Duolanasayi gold deposit, 60 km NW of Habahe County, Xinjiang Uygur Autonomous Region, is a mid-large-scale gold deposit controlled by brittle-ductile shearing, and superimposed by albitite veins and late-stage magma hydrothermal solutions. There are four types of pyrite, which are contained in the light metamorphosed rocks (limestone, siltstone), altered-mineralized rocks (chlorite-schist, altered albite-granite, mineralized phyllite), quartz veins and carbonatite veinlets. The pyrite is the most common ore mineral. The Au-barren pyrite is present mainly in a simple form and gold-bearing pyrite is present mainly in a composite form. From the top downwards, the pyrite varies in crystal form from {100} and {210}+{100} to {210}+{100}+{111} to {100}+{111}. Geochemical studies indicate that the molecular contents of pyrite range from Fe1.057S2 to Fe0.941S2. Gold positively correlates with Mn, Sr, Zn, Te, Pb, Ba and Ag. There are four groups of trace elements: Fe-Cu-Sr-Ag, Au-Te-Co, As-Pb-Zn and Mn-V-Ti-Ba-Ni-Cr in pyrite. The REE characteristics show that the total amount of REE (ΣREE) ranges from 32.35×10 -6 to 132.18×10 -6; LREE/HREE, 4.466-9.142; (La/Yb)N, 3.719-11.133; (Eu/Sm)N, 0.553-1.656; (Sm/Nd)N, 0.602-0.717; La/Yb, 6.26-18.75; δEu, 0.628-2.309; δCe, 0.308-0.816. Sulfur isotopic compositions (δ 34S=-2.46‰--7.02‰) suggest that the sulfur associated with gold mineralization was derived from the upper mantle or lower crust.

  6. Structural and metamorphic evolution of the Orocopia Schist and related rocks, southern California: Evidence for late movement on the Orocopia fault (United States)

    Jacobson, Carl E.; Dawson, M. Robert


    The Pelona, Orocopia, and Rand Schists (POR schists) of southern California and southwesternmost Arizona are late Mesozoic or early Tertiary subduction complexes that underlie Precambrian to Mesozoic continental basement along the low-angle Vincent-Chocolate Mountains (VCM) fault system. The VCM faults are often considered to be remnants of the original subduction zone, but recent work indicates that many have undergone substantial postsubduction reactivation. In the Orocopia Mountains, for example, the Orocopia Schist exhibits an exceptionally complex structural and metamorphic history due to multiple periods of movement along the Orocopia fault. Structures in the schist include isoclinal folds with axial-planar schistosity, open-to-tight folds that fold schistosity, penetrative stretching lineations, and crenulation lineations, all of which show a nearly 360° range in trend. Folds and lineations that trend approximately NE-SW occur throughout the schist and are thought to be part of an early phase of deformation related to subduction. Folds of this orientation show no consistent vergence. Folds and lineations that trend approximately NW-SE are concentrated near the Orocopia fault and are interpreted to have formed during exhumation of the schist. The NW-SE trending folds, and shear indicators in late-stage mylonite at the top of the schist, consistently verge NE. The exhumation event culminated in emplacement of the schist against brittlely deformed upper plate. Exhumation of the Orocopia Schist was accompanied by retrograde replacement of garnet, biotite, epidote, and calcic amphibole by chlorite, calcite, and sericite. Matrix amphibole has a lower Na/Al ratio than amphibole inclusions in albite, consistent with a late-stage decrease in pressure. As NE vergence in the Orocopia Mountains is associated with exhumation of the schist, the NE movement along other segments of the VCM fault may also be late and therefore have no bearing on the facing direction of the

  7. Status of geochemical modeling of groundwater evolution at the Tono in-situ tests site, Japan

    Energy Technology Data Exchange (ETDEWEB)

    Sasamoto, Hiroshi; Yui, Mikazu [Japan Nuclear Cycle Development Inst., Tokai Works, Tokai, Ibaraki (Japan); Arthur, R.C. [Monitor Scientific, L.L.C., Denver, Colorado (United States)


    Hydrochemical investigation of Tertiary sedimentary rocks at JNC's Tono in-situ tests site indicate the groundwaters are: meteoric in origin, chemically reducing at depths greater than a few tens of meters in the sedimentary rock, relatively old [carbon-14 ages of groundwaters collected from the lower part of the sedimentary sequence range from 13,000 to 15,000 years BP (before present)]. Ca-Na-HCO{sub 3} type solutions near the surface, changing to Na-HCO{sub 3} type groundwaters with increasing depth. The chemical evolution of the groundwaters is modeled assuming local equilibrium for selected mineral-fluid reactions, taking into account the rainwater origin of these solutions. Results suggest it is possible to interpret approximately the 'real' groundwater chemistry (i.e., pH, Eh, total dissolved concentrations of Si, Na, Ca, K, Al, carbonate and sulfate) if the following assumptions are adopted: CO{sub 2} concentration in the gas phase contacting pore solutions in the overlying soil zone=10{sup -1} bar, minerals in the rock zone that control the solubility of respective elements in the groundwater include; chalcedony (Si), albite (Na), kaolinite (Al), calcite (Ca and carbonate), muscovite (K) and pyrite (Eh and sulfate). It is noted, however, that the available field data may not be sufficient to adequately constrain parameters in the groundwater evolution model. In particular, more detailed information characterizing certain site properties (e.g., the actual mineralogy of 'plagioclase', 'clay' and 'zeolite') are needed to improve the model. Alternative conceptual models of key reactions may also be necessary. For this reason, a model that accounts for ion-exchange reactions among clay minerals, and which is based on the results of laboratory experiments, has also been evaluated in the present study. Further improvements of model considering ion-exchange reactions are needed in future, however. (author)

  8. Record of mid-Archaean subduction from metamorphism in the Barberton terrain, South Africa. (United States)

    Moyen, Jean-François; Stevens, Gary; Kisters, Alexander


    Although plate tectonics is the central geological process of the modern Earth, its form and existence during the Archaean era (4.0-2.5 Gyr ago) are disputed. The existence of subduction during this time is particularly controversial because characteristic subduction-related mineral assemblages, typically documenting apparent geothermal gradients of 15 degrees C km(-1) or less, have not yet been recorded from in situ Archaean rocks (the lowest recorded apparent geothermal gradients are greater than 25 degrees C km(-1)). Despite this absence from the rock record, low Archaean geothermal gradients are suggested by eclogitic nodules in kimberlites and circumstantial evidence for subduction processes, including possible accretion-related structures, has been reported in Archaean terrains. The lack of spatially and temporally well-constrained high-pressure, low-temperature metamorphism continues, however, to cast doubt on the relevance of subduction-driven tectonics during the first 1.5 Gyr of the Earth's history. Here we report garnet-albite-bearing mineral assemblages that record pressures of 1.2-1.5 GPa at temperatures of 600-650 degrees C from supracrustal amphibolites from the mid-Archaean Barberton granitoid-greenstone terrain. These conditions point to apparent geothermal gradients of 12-15 degrees C-similar to those found in recent subduction zones-that coincided with the main phase of terrane accretion in the structurally overlying Barberton greenstone belt. These high-pressure, low-temperature conditions represent metamorphic evidence for cold and strong lithosphere, as well as subduction-driven tectonic processes, during the evolution of the early Earth.

  9. Constraints on Alpine hydrothermal activity and deformation from U-Th-Pb dating of cleft monazite and xenotime (Western Alps) (United States)

    Grand'Homme, Alexis; Janots, Emilie; Bosse, Valerie; Seydoux-Guillaume, Anne-Magali; De Ascencao, Roger


    In this large-scale regional study, age of hydrothermal monazite (and xenotime) precipitation has been investigated through in-situ U-Th-Pb dating of crystals collected in 11 clefts (veins) taken in the internal and external massifs (Western Alps). The investigated clefts are composed of quartz, chlorite (± epidote), albite and millimetric accessory minerals (monazite, apatite, xenotime, anatase, rutile). Prior to dating, cleft monazite composition was thoroughly studied to reveal potential zoning. In-situ dating through different compositional domains of single monazite crystal yields well-resolved Th-Pb ages (typically with 0.1-0.3 Ma resolution) indicating for growth episodes with short duration. Comparison of U-Pb and Th-Pb dating indicates that the U-Pb systematics appears successful to date cleft monazite with low Th/U ratio (typically hand, monazite dating in the Argentera (20.6 ± 0.3 Ma) confirms for the regional diachronism observed from South to the North of the ECM in the Western Alps. First ages were here obtained for the hydrothermal activity of the internal massifs of the Western Alps. As expected from other (thermo)chronometers, hydrothermal activity in the Internal Alpine domains (Briançonnais) is older than in the ECM. In the Briançonnais zone, monazite age at 32.1 ± 0.2 Ma coincides with the exhumation along the penninic front. In the second cleft, monazite age at 23.3 ± 0.2 Ma is more complex to attribute to a specific deformation stage.

  10. Geochemical and isotopic investigations on groundwater residence time and flow in the Independence Basin, Mexico (United States)

    Mahlknecht, J.; Gárfias-Solis, J.; Aravena, R.; Tesch, R.


    The Independence Basin in the semi-arid Guanajuato state of central Mexico is facing serious groundwater resources deficiency due to an increasing demand linked to a rapid population growth and agricultural development. This problem is aggravated by an inadequate evaluation of groundwater resources in the region. Geochemistry and isotopic tracers were used in order to investigate the groundwater flow system and estimate the groundwater residence time. The groundwater is characterized by low salinity with some exceptions associated to a contribution of more saline groundwater from deep formations. The predominant reactions are CO 2 gas dissolution, carbonate dissolution, albite weathering, kaolinite and chalcedony precipitation. Six principal hydrochemical zones were recognized, which provided information on plausible recharge sources and groundwater chemical evolution. The 14C concentration varies between 19 and 94 pmc. The high 14C values indicating recent recharge are observed at the basin margins and a trend to lower 14C values is observed along the modern groundwater flow paths. The groundwater residence time according to radiocarbon estimations ranges between recent and ˜11 ka. The residence time distribution matches the regional important discharge zones west in the basin center (from Dolores Hidalgo and southwest from Doctor Mora). Hydrochemical tracers are in general agreement with the predeveloped and current hydraulic-head configuration, however, show some inconsistencies with the predeveloped head in the downgradient areas, which means that the impact by gradually increasing groundwater extraction during the last decades is reflected on radiocarbon age distribution. Geochemical evidences imply that the recharge input from the northern basin area is insignificant.

  11. The Gem Mineralogy Researching for Guatemala Jade%危地马拉翡翠的宝石矿物学研究

    Institute of Scientific and Technical Information of China (English)

    陈晶晶; 何明跃; 白志民


    利用电子探针(PXRF)、X射线粉末衍射(XRD)及红外光谱(FIR)等技术手段对危地马拉翡翠样品进行分析,并与缅甸翡翠的宝石矿物学特征进行对比研究.结果表明,危地马拉翡翠的化学成分与硬玉的基本相同.矿物组成主要为硬玉,并且含有钠长石、白云母以及少量金云母、黝帘石、榍石和方沸石等.结构主要为柱粒状变晶结构与碎裂结构,是导致其质地较粗的主要原因之一.红外光谱与缅甸翡翠的红外光谱相比有明显漂移.%The samples of Guatemala jadeite were analyzed by electron probe analysis (EP), X-ray powder diffraction (XRD) and infrared spectroscopy (IR), and compared with the gem mineralogical characteristics of the Burma jade. Which shows that the chemical compositions of jadeite are as same as the jade's in Guatemala. The main minerals in Guatemala jadeite are jade containing albite, muscovite, and few phlogopite, zoisite, titanite and analcime; the main structures are columnargrain metacryst structure and cataclastic texture structure, which is one of the mainly reasons why their texture are crude; the infrared spectroscopy of Guatemala jade is drifted obviously than the Burma jade's.

  12. Composition Analysis of Ancient Bricks, Candi Bukit Kechil, Bujang Valley, Kedah

    Directory of Open Access Journals (Sweden)

    Zuliskandar Ramli


    Full Text Available Candi Bukit Kechil or Bukit Kechil Temple is one of the temples in Bujang Valley that was built on a hill apart from Candi Bukit Pendiat (Site 17, Candi Bukit Meriam (Site 26, Candi Bukit Penjara (Site 25 and Candi Bukit Gajah Mati (Site 7. On the whole, this temple was made from bricks and based on the north-south orientation and the construction of the lotus-like structure, it is believed that this temple is of Buddhist religion and was built between 9th to 10th century AD. Based on GPS reading, the temple’s location is N5 37.129 E100 27.324. Analysis on the bricks of the temple was performed to determine whether the bricks used local raw material or otherwise, as well as to find out the physical condition of the bricks, particularly their burning method. As such, two analysis techniques were conducted, namely the X-Ray Diffraction and the X-Ray Fluorescence method that respectively determined the mineral content of the bricks as well as the major and trace element content of the bricks. Analysis shows that the minerals contained in the brick samples of Candi Bukit Kechil comprise of quartz, muscovite, albite and kaolinite. The presence of the kaolinite mineral shows that there are bricks that were baked at temperatures less than 550°C and this shows that open burning was used. The analyses of major and trace element content show that the raw material used are local raw material and the sources of the raw material were obtained from the area of the Bujang River basin and the areas around Mukim Merbok and Mukim Bujang.

  13. Nanomineralogy as a new dimension in understanding elusive geochemical processes in soils: The case of low-solubility-index elements

    Energy Technology Data Exchange (ETDEWEB)

    Schindler, Michael; Hochella Jr., Michael F.


    Nanomineralogy is a new dimension in understanding chemical processes in soils. These processes are revealed at the nanoscale within the structures and compositions of phases that heretofore were not even known to exist in the soils in which they are found. The discovery and understanding of soil chemistry in this way is best accessible via a combination of focused ion beam technology (for sample preparation) and high resolution, analytical transmission electron microscopy (for phase identification). We have used this scientific framework and these techniques to decipher past and present chemical processes in a soil in Sudbury, Ontario, Canada that has been impacted by both smelter contamination (acidification) and subsequent remediation within the past century. In this study, we use these methods to investigate mobilization and sequestration of the relatively immobile elements Al, Ti and Zr. In a micrometer-thick alteration layer on an albite grain, a first generation of clay minerals represents weathering of the underlying mineral prior to the acidification of the soils. Complex assemblages of Ti- and Zr-bearing nanophases occur on the surfaces of Fe-(hydr)oxide crystals and are the result of the dissolution of silicates and oxides and the mobilization of Ti- and Zr-bearing colloids under acidic conditions. These phases include anatase (TiO2), kleberite (Fe3+Ti6O11(OH)5) Ti4O7, baddelyite (ZrO2), a structural analogue to kelyshite (NaZr[Si2O6(OH)]) and authigenic zircon (ZrSiO4). Subsequent remediation of the acidic soils has resulted in the sequestration of Al and in the neoformation of the clay minerals kaolinite, smectite and illite. These complex mineral assemblages form a porous layer that controls the interaction of the underlying mineral with the environment.

  14. Secondary mineralization and hydrothermal alteration in the Reydarfjordur drill core, eastern Iceland (United States)

    Mehegan, James M.; Robinson, Paul T.; Delaney, John R.


    Deep crustal drilling in eastern Iceland has allowed study of a fossil hydrothermal system at a constructive plate margin. The drilled sequence consists of partly to completely altered subaerial lava flows, basaltic dikes, and minor clastic material. Alteration and secondary mineralization are most intense in the flow top breccias where water/rock ratios are presumed to have been the highest. In the upper portion of the cored sequence (to a depth of about 1200 m) alteration is characterized by the deposition of clay minerals ± calcite ± quartz ± laumontite into open spaces such as vugs and vesicles. Low-temperature zeolites, such as stilbite, epistilbite, mordenite, and heulandite, are also present but are restricted to the upper 500 m of the drill core. Below 1200 m, alteration is characterized by the dissolution and replacement of both primary minerals and earlier authigenic minerals, followed by partial filling of dissolution cavities. Early mineral assemblages consist of epidote ± quartz ± prehnite ± chlorite ± albite, and a later superimposed assemblage consists of calcite + laumontite ± anhydrite. Authigenic sphene, pyrite, chalcopyrite, pumpellyite, actinolite, and wairakite also occur sporadically in the cored sequence. Secondary mineral assemblages and temperature measurements of fluid inclusions suggest a maximum temperature of alteration of about 300°C. Fluid inclusion compositions indicate that the geothermal fluid was meteoric water with very low salinities and high calcium activities. Iron activities and oxygen fugacities were highest in the deeper portions of the systems. The mineral paragenesis suggests that the fluid composition, temperature, and PCO2 varied significantly with time. The thermal energy for the geothermal system was probably derived from a high-level magma chamber associated with nearby Thingmuli volcano. Local contact metamorphism, indicated by the formation of garnet, occurred during late stage emplacement of dikes into

  15. The geological setting and style of copper mineralization at the Bushman group of deposits, northeastern Botswana (United States)

    Barton, J. M.; Blaine, J. L.; Doig, R.; Byron, C. L.


    The Bushman group of CuPbZn deposits occur within the north-northeasterly trending Bushman shear zone in northeastern Botswana. The deposits are hosted by a sliver of sheared and altered, carbonate rocks and chloritic and graphitic schists that resemble and are presumed correlative with metasedimentary rocks of the Matsitama schist belt to the east. This sliver is surrounded by sheared and altered granitic gneisses. Within the sliver, the mineralized zones are a chalcopyrite and pyrite bearing quartz-calcite±alkali feldspar vein breccias near the sheared contact between the carbonate rocks and the chloritic and graphitic schists. Elsewhere within the granitic gneisses, those zones are marked by barren quartz breccias surrounded by a zone dominated by red, turbid orthoclase in turn surrounded by a zone dominated by green epidote. Initially hydrothermal alteration propylitized the host rocks and then porphyroblasts of orthoclase, albite and quartz grew with the introduction of calcite. Away from the mineralized zones, four generations of veins occur, the first two directly traceable to CuPbZn mineralization and the third carrying galena and sphalerite. Isotopic data suggest that the protolith of the granitic gneisses was emplaced sometime between about 2.57 Ga and 2.3 Ga ago. After this protolith was deformed and metamorphosed, CuPbZn mineralization occurred about 1926 Ma ago from fluids at a temperature of about 360°C. The Pb isotopic compositions of the sulfide minerals indicate that the fluids giving rise to the CuPbZn mineralization were possibly the same as those giving rise to Pb and Zn mineralization. In both instances, however, the Pb came from several sources. More recently, shear zones parallel to the Bushman shear zone may have controlled in part the emplacement of kimberlite pipes.

  16. Nitrogen distribution between aqueous fluids and silicate melts (United States)

    Li, Yuan; Huang, Ruifang; Wiedenbeck, Michael; Keppler, Hans


    The partitioning of nitrogen between hydrous fluids and haplogranitic, basaltic, or albitic melts was studied at 1-15 kbar, 800-1200 °C, and oxygen fugacities (fO2) ranging from the Fe-FeO buffer to 3log units above the Ni-NiO buffer. The nitrogen contents in quenched glasses were analyzed either by electron microprobe or by secondary ion mass spectrometry (SIMS), whereas the nitrogen contents in fluids were determined by mass balance. The results show that the nitrogen content in silicate melt increases with increasing nitrogen content in the coexisting fluid at given temperature, pressure, and fO2. Raman spectra of the silicate glasses suggest that nitrogen species change from molecular N2 in oxidized silicate melt to molecular ammonia (NH3) or the ammonium ion (NH4+) in reduced silicate melt, and the normalized Raman band intensities of the nitrogen species linearly correlate with the measured nitrogen content in silicate melt. Elevated nitrogen contents in silicate melts are observed at reduced conditions and are attributed to the dissolution of NH3/NH4+. Measured fluid/melt partition coefficients for nitrogen (DNfluid/ melt) range from 60 for reduced haplogranitic melts to about 10 000 for oxidized basaltic melts, with fO2 and to a lesser extent melt composition being the most important parameters controlling the partitioning of nitrogen. Pressure appears to have only a minor effect on DNfluid/ melt in the range of conditions studied. Our data imply that degassing of nitrogen from both mid-ocean ridge basalts and arc magmas is very efficient, and predicted nitrogen abundances in volcanic gases match well with observations. Our data also confirm that nitrogen degassing at present magma production rates is insufficient to accumulate the atmosphere. Most of the nitrogen in the atmosphere must have degassed very early in Earth's history and degassing was probably enhanced by the oxidation of the mantle.

  17. Luminescence properties of feldspars from the Northeast region of Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Santana, S T; Khoury, H J; Sullasi, H L; Guzzo, P L, E-mail:


    The aim of this study is to investigate the thermoluminescence (TL) and infrared-stimulated luminescence (IRSL) properties of three types of feldspars from the districts of Solonopole and Parelhas located in the Northeast region of Brazil in order to propose a preheat procedure to minimize the anomalous fading effect in these materials. The feldspar samples were characterized by X-ray diffraction (XRD) and X-ray fluorescence spectrometry (XRF). The XRD analysis showed that the feldspar from Solonopole and one of the samples from the Parelhas district were classified as microcline (K-feldspar). The other sample from Parelhas was classified as albite (Na-feldspar) mixed with low concentration of muscovite and quartz. Studies of the fading effects in TL and IRSL signals for 30 days and preheating effects from 50 to 250{sup 0}C for 10 minutes were carried out with these samples. The results show that preheating at 125{sup 0}C is sufficient to avoid the 30 days fading. The TL and IRSL dose responses for {sup 60}Co gamma radiation were studied in the range of 1 to 400 Gy. The results showed a linear response in the range of 1 to 100 Gy for the two types of Parelhas feldspars and from 50 to 400 Gy for the Solonopole feldspar. The low sensitivity showed by the feldspar from Solonopole is discussed in relation to its mineralogical composition. It is concluded that the TL and IRSL sensitivities are not associated with K- and Na- types of feldspar. The results of this paper will contribute to a standardized moderate annealing treatment for retrospective dosimetry and dating.

  18. Metamorphic Evolution of Garnet-bearing Epidote-Barroisite Schist from the Meratus Complex in South Kalimantan, Indonesia

    Directory of Open Access Journals (Sweden)

    Nugroho Imam Setiawan


    Full Text Available This paper presents metamorphic evolution of metamorphic rocks from the Meratus Complex in South Kalimantan, Indonesia. Eight varieties of metamorphic rocks samples from this location, which are garnet-bearing epidote-barroisite schist, epidote-barroisite schist, glaucophane-quartz schist, garnet-muscovite schist, actinolite-talc schist, epidote schist, muscovite schist, and serpentinite, were investigated in detail its petrological and mineralogical characteristics by using polarization microscope and electron probe micro analyzer (EPMA. Furthermore, the pressure-temperature path of garnet-bearing epidote-barroisite schist was estimated by using mineral parageneses, reaction textures, and mineral chemistries to assess the metamorphic history. The primary stage of this rock might be represented by the assemblage of glaucophane + epidote + titanite ± paragonite. The assemblage yields 1.7 - 1.0 GPa in assumed temperature of 300 - 550 °C, which is interpreted as maximum pressure limit of prograde stage. The peak P-T condition estimated on the basis of the equilibrium of garnet rim, barroisite, phengite, epidote, and quartz, yields 547 - 690 °C and 1.1 - 1.5 GPa on the albite epidote amphibolite-facies that correspond to the depth of 38 - 50 km. The retrograde stage was presented by changing mineral compositions of amphiboles from the Si-rich barroisite to the actinolite, which lies near 0.5 GPa at 350 °C. It could be concluded that metamorphic rocks from the Meratus Complex experienced low-temperature and high-pressure conditions (blueschist-facies prior to the peak metamorphism of the epidote amphibolite-facies. The subduction environments in Meratus Complex during Cretaceous should be responsible for this metamorphic condition.

  19. Gold deposits in the late Archaean Nzega-Igunga greenstone belt, central plateau of tanzania

    Energy Technology Data Exchange (ETDEWEB)

    Feiss, P.G.; Siyomana, S.


    2.2 m oz of gold have been produced, since 1935, from late Archaean (2480-2740 Ma) greenstone belts of the Central Plateau, Tanzania. North and east of Nzega (4/sup 0/12'S, 3/sup 0/11'E), 18% of the exposed basement, mainly Dodoman schists and granites, consists of metavolcanics and metasediments of the Nyanzian and Kavirondian Series. Four styles of mineralization are observed. 1. Stratabound quartz-gold veins with minor sulfides. Host rocks are quartz porphyry, banded iron formation (BIF), magnetite quartzite, and dense, cherty jasperite at the Sekenke and Canuck mines. The Canuck veins are on strike from BIF's in quartz-eye porphyry of the Igusule Hills. 2. Stratabound, disseminated gold in coarse-grained, crowded feldspar porphyry with lithic fragments and minor pyrite. At Bulangamilwa, the porphyry is conformable with Nyanzian-aged submarine (.) greenstone, volcanic sediment, felsic volcanics, and sericite phyllite. The deposits are on strike with BIF of the Wella Hills, which contains massive sulfide with up to 15% Pb+Zn. 3. Disseminated gold in quartz-albite metasomes in Nyanzian greenstones. At Kirondatal, alteration is associated with alaskites and feldspar porphyry dikes traceable several hundred meters into post-Dodoman diorite porphyry. Gold is with pyrite, arsenopyrite, pyrrhotite, minor chalcopyrite, and sphalerite as well as tourmalinite and silica-cemented breccias. 4. Basal Kavirondian placers in metaconglomerates containing cobbles and boulders of Dodoman and Nyanzian rocks several hundred meters up-section from the stratabound, disseminated mineralization at Bulangamilwa.

  20. Process optimization of reaction of acid leaching residue of asbestos tailing and sodium hydroxide aqueous solution

    Institute of Scientific and Technical Information of China (English)

    DU GaoXiang; ZHENG ShuiLin; DING Hao


    Silica is the major component of the acid leaching residue of asbestos tailing. The waterglass solution can be prepared by the reaction of the residue with sodium hydroxide aqueous solution. Compared to the high temperature reaction method, this process is environmental friendly and low cost. In this paper, the reaction process of the residue and the sodium hydroxide aqueous solution is optimized. The op-timum reaction process parameters are as follows: the usage of sodium hydroxide is 26.4 g/100 g acid leaching residue, the reaction temperature is 90℃, the reaction time is 1 h, and the ratio of the liq-uid/solid is 2.0. The significance sequence of the process parameters to the alkali leaching reaction effect is the usage of sodium hydroxide > the ratio of the liquid/solid > the reaction time > the reaction temperature. The significance sequence to the leaching ratio of SiO2 is the ratio of the liquid/solid > the usage of sodium hydroxide > the reaction time > the reaction temperature. The significance sequence to the modulus of the sodium silicate is the ratio of the liquid/solid > the usage of sodium hydroxide > the reaction time > the reaction temperature. Under the optimum conditions, the leaching ratio of the SiO2 is 77.5%, and the modulus of the sodium silicate is 3.15. The XRD analysis result indicates that the major components of the alkali leaching residue are serpentine, talc, quartz and some albite.

  1. Characterisation of Na-metasomatism in the Sveconorwegian Bamble Sector of South Norway

    Directory of Open Access Journals (Sweden)

    Ane K. Engvik


    Full Text Available Na-metasomatism in the form of albitisation is regionally extensive in the Precambrian crust of southern Scandinavia and is particularly widespread in the Bamble Sector, the Kongsberg-Modum Sector and the Norwegian part of the Mylonite Zone. Sites of albitisation outside these belts are associated with hydrothermal breccia pipes and fracture-bound alteration. The albitites are composed of near end-member sodic plagioclase (An0–5Ab94–99 with minor carbonate (calcite and dolomite, rutile, clinopyroxene (En30Fs21–23Wo47–49, amphibole (edenite-pargasite, quartz, titanite, tourmaline, epidote (Fe3+ = 0.20–0.85 a.p.f.u and chlorite (Mg# = 0.81–0.89. The albitites have been studied in detail in the region around the town of Kragerø, and are described as albitisation along veins, as breccias, albitic felsites, massive carbonate-bearing albitites and megascale clinopyroxene-titanite-bearing albitite. The strong fluid control on their formation is illustrated by the veining and mineral replacement reactions, showing fluid transport by a H2O-CO2 fluid rich in Na, depleting Fe and Mg from the host rock, in accordance with calculated mass transfer. A study of the mineralogical replacement reactions in combination with a regional compilation has demonstrated the relationship between metasomatic processes and the formation of apatite, rutile and Fe deposits. The albitites occur spatially associated with other metasomatic rocks such as scapolitised metagabbros. We document that metasomatism is an important mineral- and rock-forming process in the continental crust, which in the Bamble Sector is a part of the tectonometamorphic evolution of the Sveconorwegian orogen.

  2. Geology, mineralization, and fluid inclusion characteristics of the Skrytoe reduced-type W skarn and stockwork deposit, Sikhote-Alin, Russia (United States)

    Soloviev, Serguei G.; Kryazhev, Sergey G.


    The Skrytoe deposit (>145 Kt WO3, average grade 0.449% WO3) in the Sikhote-Alin orogenic system (Eastern Russia) is situated in a metallogenic belt of W, Sn-W, Au, and Au-W deposits formed in a late to post-collisional tectonic environment after cessation of active subduction. It is localized within a mineralized district of reduced-type skarn W and veined Au (±W) deposits and occurrences related to the Early Cretaceous ilmenite-series plutonic suite. The deposit incorporates large stockworks of scheelite-bearing veinlets related to propylitic (amphibole, chlorite, quartz) and phyllic (quartz, sericite, albite, apatite, and carbonate) hydrothermal alteration. The stockwork cuts flat-lying mafic volcanic rocks and limestone partially replaced by pyroxene skarn that host the major W orebodies. Scheelite is associated with pyrrhotite and/or arsenopyrite, with minor chalcopyrite and other sulfide minerals; the late phyllic stage assemblages hosts Bi and Au mineralization. The fluid evolution included low-salinity moderate-temperature, moderate-pressure (˜370-390 °C, ˜800 bars) methane-dominated carbonic-aqueous fluids that formed post-skarn propylitic alteration assemblages. Then, at the phyllic stage, there has been an evolution from methane-dominated, moderate-temperature (330-360 °C), low-salinity (water (δ18OH2O = +7.4 to +7.7 ‰), and dominantly crustal-derived source of sulfur (δ34S = -4.6 to -2.9 ‰) in the hydrothermal fluids. This is consistent with the development of larger, longer crystallizing crustal intermediate to felsic magma chambers in the late to post-collisional tectonic environment, with their protracted magmatic evolution advancing magmatic differentiation and partitioning of W into magmatic-hydrothermal fluid. The dominating role of the crustal-derived magmatic water, sulfur, and carbon appears to be an important feature of reduced W skarn deposits related to ilmenite-series granitoids.

  3. Intensive low-temperature tectono-hydrothermal overprint of peraluminous rare-metal granite: a case study from the Dlhá dolina valley (Gemericum, Slovakia

    Directory of Open Access Journals (Sweden)

    Breiter Karel


    Full Text Available A unique case of low-temperature metamorphic (hydrothermal overprint of peraluminous, highly evolved rare-metal S-type granite is described. The hidden Dlhá dolina granite pluton of Permian age (Western Carpathians, eastern Slovakia is composed of barren biotite granite, mineralized Li-mica granite and albitite. Based on whole-rock chemical data and evaluation of compositional variations of rock-forming and accessory minerals (Rb-P-enriched K-feldspar and albite; biotite, zinnwaldite and di-octahedral micas; Hf-(Sc-rich zircon, fluorapatite, topaz, schorlitic tourmaline, the following evolutionary scenario is proposed: (1 Intrusion of evolved peraluminous melt enriched in Li, B, P, F, Sn, Nb, Ta, and W took place followed by intrusion of a large body of biotite granites into Paleozoic metapelites and metarhyolite tuffs; (2 The highly evolved melt differentiated in situ forming tourmaline-bearing Li-biotite granite at the bottom, topaz-zinnwaldite granite in the middle, and quartz albitite to albitite at the top of the cupola. The main part of the Sn, Nb, and Ta crystallized from the melt as disseminated cassiterite and Nb-Ta oxide minerals within the albitite, while disseminated wolframite appears mainly within the topaz-zinnwaldite granite. The fluid separated from the last portion of crystallized magma caused small scale greisenization of the albitite; (3 Alpine (Cretaceous thrusting strongly tectonized and mylonitized the upper part of the pluton. Hydrothermal low-temperature fluids enriched in Ca, Mg, and CO2 unfiltered mechanically damaged granite. This fluid-driven overprint caused formation of carbonate veinlets, alteration and release of phosphorus from crystal lattice of feldspars and Li from micas, precipitating secondary Sr-enriched apatite and Mg-rich micas. Consequently, all bulk-rock and mineral markers were reset and now represent the P-T conditions of the Alpine overprint.

  4. Cooling rates and crystallization dynamics of shallow level pegmatite-aplite dikes, San Diego County, California (United States)

    Webber, Karen L.; Simmons, William B.; Falster, Alexander U.; Foord, Eugene E.


    Pegmatites of the Pala and Mesa Grande Pegmatite Districts, San Diego County, California are typically thin, sheet-like composite pegmatite-aplite dikes. Aplitic portions of many dikes display pronounced mineralogical layering referred to as "line rock," characterized by fine-grained, garnet-rich bands alternating with albite- and quartz-rich bands. Thermal modeling was performed for four dikes in San Diego County including the 1 m thick Himalaya dike, the 2 m thick Mission dike, the 8 m thick George Ashley dike, and the 25 m thick Stewart dike. Calculations were based on conductive cooling equations accounting for latent heat of crystallization, a melt emplacement temperature of 650 °C into 150 °C fractured, gabbroic country rock at a depth of 5 km, and an estimated 3 wt% initial H2O content in the melt. Cooling to -5 cm/s. Crystal size distribution (CSD) studies of garnet from layered aplites suggest growth rates of about 10-6 cm/s. These results indicate that the dikes cooled and crystallized rapidly, with variable nucleation rates but high overall crystal-growth rates. Initial high nucleation rates coincident with emplacement and strong undercooling can account for the millimeter-size aplite grains. Lower nucleation rates coupled with high growth rates can explain the decimeter-size minerals in the hanging walls, cores, and miarolitic cavities of the pegmatites. The presence of tourmaline and/or lepidolite throughout these dikes suggests that although the melts were initially H2O-undersaturated, high melt concentrations of incompatible (or fluxing) components such as B, F, and Li (±H2O), aided in the development of large pegmatitic crystals that grew rapidly in the short times suggested by the conductive cooling models.

  5. Allanite from the El Muerto Pegmatite, Oaxaca, Mexico: A Potential New Standard for 232Th-208Pb Dating by LA-ICP-MS (United States)

    Price, J.; Crowley, J. L.; Solari, L.; Prol-Ledesma, R.


    Allanite dating may be important to studies addressing tectonomagmatic evolution, provenance of monocyclic sediment, and mineral weathering. Obtaining accurate allanite ages by SIMS has been challenging and time-consuming due to the mineral's extreme chemical variability which often prevents finding adequately matrix-matched standards. Isotopic measurements by LA-ICP-MS minimize the need for standards of nearly identical composition to the unknown allanite being analyzed, and it is done relatively rapidly. Dating by LA-ICP-MS requires high quality standards for isotopic fractionation corrections. However, readily accessible and well characterized allanite standards are scarce. We investigated gemstone allanite from the El Muerto pegmatite, Oaxaca, Mexico, as a potential new geochronology standard for 232Th-208Pb allanite dating by LA-ICP-MS. Compositional homogeneity was thoroughly investigated by scanning and backscatter electron microscopy, cathodoluminescence, quantitative and qualitative energy dispersive x-ray spectroscopy, electron microprobe, and LA-ICP-MS. The possibility of metamictization was investigated by extensive X-ray diffraction analyses. The El Muerto allanite was U-Pb dated by ID-TIMS, with common Pb ratios determined from cogenetic K-feldspar by ID-TIMS and LA-MC-ICP-MS. Future work includes Th-Pb dating by ID-TIMS. The samples investigated are homogeneous with respect to major and trace elements. Major element compositional results are generally in agreement with published values, and no metamictization was identified despite the allanite being nearly 1 Ga. The only limitation of the El Muerto allanite is that it contains small, generally <100 μm, scarce inclusions of quartz, calciothorite, albite, calcite, and biotite. However, these grains are easily recognized and avoided during LA-ICP-MS analyses. Based on these results, the El Muerto allanite has the potential to serve as a standard for LA-ICP-MS dating.

  6. Petrology of blueschist and meta-greywacke along the Turkmeni-Ordib fault (Turkmeni area, SE of Anarak

    Directory of Open Access Journals (Sweden)

    Fereshteh Bayat


    Full Text Available Introduction The occurrence of blueschist metamorphic facies is believed to mark the existence of former subduction zones. This facies is represented in the main constituents of subduction-accretion complexes, where it occurs in separate tectonic sheets, imbricated slices, lenses, or exotic blocks within a serpentinite mélange (Volkova et al., 2011. The evidence of the presence and maturity of Paleo- Tethys oceanic crust in the CEIM (define this in Paleo-Tethys branches, subduction and collision has been studied by various authors (Bagheri, 2007; Zanchi et al., 2009; Bayat and Torabi, 2011; Torabi 2011. Late Paleozoic blueschists have recognized in the western part of the CEIM (e. g. Anarak, Chupanan and Turkmeni in linear trends. Metamorphic rocks of the Turkmeni area (SE of Anarak are composed of blueschist and meta-greywacke and are situated along the Turkmeni-Ordib fault associated with Paleozoic rock units and serpentinized peridotite bodies. Turkmeni blueschist and meta-greywackes have not been studied by previous workers. The Turkmeni blueschists consist of albite, winchite, actinolite and epidote. Granoblastic, nematoblastic and lepidoblastic are main textures in these rocks. Winchite is found in the matrix and around epidote grains. This sodic-calcic amphibole serves as an index mineral in blueschist facies. Actinolite and epidote formed during retrograde metamorphism of blueschists in the greenschist facies. The mineral assemblage of albite, epidote, chlorite and phengite ± garnet is present in meta-greywackes in the Turkmeni blueschists. Veins of garnet, muscovite, quartz and opaque minerals are extensive in these rocks. Epidote and chlorite formed in meta-greywackes by retrograde metamorphism in the greenschist facies. The aim of the present study is to determine the petrological and geochemical characteristics, P-T condition of blueschists and meta-greywackes, as well as the geotectonic setting of primary basaltic rocks of the

  7. 准噶尔盆地西北缘下二叠统油气储层中火山物质蚀变及控制因素%Alteration of volcanics and its controlling factors in the Lower Permian reservoirs at northwestern margin of Junggar Basin

    Institute of Scientific and Technical Information of China (English)

    朱世发; 朱筱敏; 吴冬; 刘英辉; 李盼盼; 姜淑贤; 刘学超


    通过岩心分析、显微镜下观察(常规、铸体薄片和扫描电镜)、岩石地球化学分析测试等技术手段,以准噶尔盆地西北缘下二叠统油气储层为实例,研究了火山岩、火山碎屑岩和火山岩屑质砂砾岩中的火山玻璃、火山碎屑、长石以及辉石、角闪石等火山物质的低温-埋藏蚀变作用。镜下观察发现,在含火山物质油气储层中,常见对储集空间具有重要影响的自生矿物主要有绿泥石、沸石(包括方沸石、片沸石和浊沸石)、方解石、钠长石和自生的石英。结合共生关系、元素组成和元素迁移,分析了自生矿物的微观特征和成因,建立了火山物质蚀变的成岩演化序列,可以概括为:①火山玻璃水化-蒙脱石化-沸石化及各种沸石的转化---钠长石化;②铁镁矿物影响的绿泥石化;③长石蚀变向绿泥石和方解石转化,后期发生钠长石化。在研究区,火山物质的蚀变和自生矿物的析出与中-基性的母岩物质组成密切相关,并受地层温度、压力、孔隙水的化学性质控制。研究火山物质蚀变的产物、蚀变过程及控制因素,能够明确含火山物质的油气储层质量差异机理,为优质储层预测提供科学的依据。%Based on observations of available cores ,thin-sections and SEM and analysis of rock geochemistry ,we studied low-temperature-burial metamorphism ( alteration ) of volcanics in the Lower Permian at northwestern margin of Junggar Basin .These volcanics include volcanic glass , volcanic clasts , feldspar , and mafic minerals such as pyroxene and horn-blende,etc.,which originate from lavas,pyroclastic rocks,and volcaniclastic sandstones or conglomerates .In oil/gas reservoirs containing volcanics ,the authigenic minerals that are common but important to pore spaces include chlorite ,ze-olites(like analcime,heulandite,and laumontite),calcite,albite,and authigenic quartz.Based on

  8. Well-logging responses and reservoir effects of rhyolite's diagenesises of Yingcheng Formation(Kly)in the Songliao Basin%松辽盆地营城组流纹岩成岩作用的测井响应及其储层效应

    Institute of Scientific and Technical Information of China (English)

    瞿雪姣; 王璞珺; 修立军; 唐华风; 高有峰


    Through observation of well core and thin sections and study of well-logging responses, we found that three kinds of diagenesises'well-logging responses are prominently, includes diagenetic albitization of kfeldspars, amygdules and fractures filled with quartz and matrix and/or phanerocrysts alternated by calcite, while denudation and devitrification are associated with other diagenesises in rhyolite. Diagenetic albitization of kfeldspars characterized as Na/K>l in ECS log and the stronger of the alternation the larger of the ratio,and the electrical resistivity is low, logging porosity shows a single peak in histogram. The features of amygdules and fractures filled with quartz includes high density, low logging porosity and low neutron in the cross-plots of DEN versus AC and Pige versus CN,the electrical resistivity toothly nearly to straight and mainly between 40 fl ? M and 100 fl ? M. Matrix and/orphanerocrysts alternated by calcite indicates the Ca curve smoothly and straightly and diverged the base line obviously,the conventional well-logging responses shows low electrical resistivity 、 low density,high acoustictime and high logging porosity. As a result of diagenetic albitization of kfeldspars, the reservoir quality improved overally, especially for the tight zone,the theoretical maximum increment of porosity is 6. 8%,the actual increment of porosity is 0. 15%'-0. 46%. Amygdules and fractures filled with quartz deteriorate the reservoir quality. The reservoir effect of matrix and/or phanerocrysts alternated by calcite mainly determined by the dissolution degree, the porosity theoretically reduced about 46% after amorphous silica in matrix alternated by calcite, the actual reduction of porosity is about 2. 3%.%岩心、薄片观察和测井响应关系研究发现,钾长石钠长石化、石英充填、方解石交代是流纹岩中三种测井响应特征明显的成岩作用,与其伴生的还有溶蚀和基质脱玻化作

  9. Source of Ore-Forming Materials of Tongchang Copper Ore Deposit in Southern Shaanxi Province, China%陕南铜厂铜矿床成矿物质来源探讨

    Institute of Scientific and Technical Information of China (English)

    叶霖; 杨玉龙; 高伟; 刘铁庚


    albite rocks in the mine. There are two kinds of chalcopyrites with different REE patterns, one is enriched in LREE and the other has relatively flat REE pattern. The pyrite grains hosted in internal and external contact zones of the diorite intrusion have different Co/Ni ratios, suggesting multiple sources of ore-forrning materials. Analyzing on the background values of those ore-forming elements in various geological bodies indicates that ore-forming material is mainly from the spilite and minor from the diorite. Secondly, the chalcopyrite is characterized by obvious negative Eu anomalies and its δEu value is much lower than those of the diorite and spilite. The depletion of Eu is likely related to greisenization and albitization caused by volatile fluids during mineralization. Furthermore, Y/Ho ratios of the chalcopyrite are similar to those of albite rocks, implying the close relationship between copper mineralization and Na replacement. Thirdly, due to the inheritance of the trace elements feature from source of ore-forming mineralizing materials, the Ni and Co content in the chalcopyrite is n-n×10 times than in the pyrite, corresponding to that in Cu - Ni sulfide type deposit and different from that in skarn-type, porphyry-type, volcanic-subvolcanic hydrothermal type as well as VMS Cu deposit. The metallogenic model of Tongchang copper deposit can be listed as following. During the Hercynian period, with the closure, subduction and collision of Mian-Lue ancient oceanic basin, the dutile-brittle thrusting nappe structure and strike-slip fault were formed in Mian-Lue-Ning area. The metasomatism of mixed hydrothermal by regional metamorphic fluid and rainwater, which rich in Na+ , K+ and CO2, resulted in the translation of ore-forming materials (e. G. Cu and Ni) from strata of Guojiagou Group and spilite (and diorite) to form the metallogenic hydrothermal fluid. The hydrothermal fluid was characterized by low temperature and salinity, and enriched in ore

  10. Modelización del proceso de episienitización (decuarcificación-albitización: formulación cinética y transporte advectivo en medio continuo

    Directory of Open Access Journals (Sweden)

    Caballero, J. M.


    Full Text Available The development of episyenites from Sierra de Guadarrama has been modelized. The process mainly consists in a coupled process of dequartztification-albitization. The model is based on pure advective mass transport in a continuum medium, where the reactive process is formulated from a kinetic point of view. It is demonstrated the possibility of its formation through the action of low-salinity fluids (2,32 wt % NaCl equiv., partially equilibrated with a biotite monzogranite, linked to isobaric reaction paths across negative geothermal gradients, intersecting the quartz retrograde solubility field, and associated to a quick fluid-resident mobilisation due to the environment tectonic opening. The model explains the albitic nature of the alteration against former models. These predict microcline formation from the gradient relations ∂logKmic/∂T > ∂logKab/∂T (0.05739 and 0.05735 and ∂logKKCl/∂T NaCl/∂T (-0.038 and -0.036. Albite formation arises from the anortite component presence, because ∂logKan/∂T =0,1293 ≻ ∂logKmic/∂T. Non-equilibrium relations are very small, which implies that alteration intensity arises from the circulation of huge fluid volumes. This process feature together the kinetic rate constants result in a small change, spatial and temporal, of the fluid composition, being practically null for its main components (Na, K and, subordinately to these, the pH. The model also shows the necessity of handling geochemical systems as complex as possible. In this way, the proposed aqueous speciation proves that pH evolution along decreasing temperature is not necessarily acid, but inlet fluid pH dependent due to the calculated concentrations show that its behaviour mainly depends as much from Hel as from the NaOH base dissociation.Se modeliza teóricamente la formación de las episienitas de la Sierra de Guadarrama, consistente básicamente en un proceso acoplado de decuarcificaci

  11. Melt Segregation & LPO in Anorthite-Basalt Deformed in Torsion (United States)

    Zimmerman, M. E.; Kohlstedt, D. L.


    Deformation in the middle and lower crust is in large part controlled by the rheology of feldspar. Seismic studies have shown that the middle crust of orogenic belts is partially molten. Structural studies of mylonites and migmatites from these terrains record large strain deformation. Therefore, we performed torsional shear deformation experiments on fine grained (10 μ m) samples of Beaver Bay anorthite (An70) +/- 10 vol% basalt to shear strains γ = 2-6 to investigate the development of lattice preferred orientation (LPO) and melt segregation at large shear strains. We performed experiments in a gas medium apparatus equipped with an internal torque cell at T = 1450 K, P = 300 MPa, and constant twist rate. Melt segregated in the An70 + basalt samples into melt-rich bands oriented at ˜20° to the shear plane and antithetic to the shear direction. The spacing between bands is ˜0.5 mm. Distortion of the iron jacket demonstrates that strain localized in the melt-rich bands. We determined the LPO of An70 with scanning electron microscopy using electron back scatter diffraction (SEM-EBSD). In patterns from an An70+ basalt sample deformed to γ ≈ 2.5, (001) planes are aligned subparallel to the shear plane and [100] axes are concentrated close to the shear direction. Both the (001) and the [100] are rotated counter clockwise from the shear direction by 20-25° . The formation of melt-rich bands is consistent with results from simple shear experiments on olivine + chromite + basalt and olivine + FeS +/- basalt, as well as An70 + basalt and indicates that deformation can drive melt segregation. Deformation drives the self organization of melt-rich bands and decreases the effective viscosity of the rock. The LPO is consistent with results from experiments on albite in shear and anorthite in compression and compatible with slip dominantly on (001) with [100] as the slip direction. A similar back rotation, attributed to partitioning of the strain between melt-rich and

  12. Origin and evolution of formation water at the Jujo-Tecominoacan oil reservoir, Gulf of Mexico. Part 1: Chemical evolution and water-rock interaction

    Energy Technology Data Exchange (ETDEWEB)

    Birkle, Peter, E-mail: [Instituto de Investigaciones Electricas (IIE), Gerencia de Geotermia, Av. Reforma 113, Cuernavaca, Morelos 62490 (Mexico); Garcia, Bernardo Martinez; Milland Padron, Carlos M. [PEMEX Exploracion y Produccion, Region Sur, Activo Integral Bellota-Jujo, Diseno de Explotacion, Cardenas, Tabasco (Mexico)


    The origin and evolution of formation water from Upper Jurassic to Upper Cretaceous mudstone-packstone-dolomite host rocks at the Jujo-Tecominoacan oil reservoir, located onshore in SE-Mexico at a depth from 5200 to 6200 m.b.s.l., have been investigated, using detailed water geochemistry from 12 producer wells and six closed wells, and related host rock mineralogy. Saline waters of Cl-Na type with total dissolved solids from 10 to 23 g/L are chemically distinct from hypersaline Cl-Ca-Na and Cl-Na-Ca type waters with TDS between 181 and 385 g/L. Bromine/Cl and Br/Na ratios suggest the subaerial evaporation of seawater beyond halite precipitation to explain the extreme hypersaline components, while less saline samples were formed by mixing of high salinity end members with surface-derived, low salinity water components. The dissolution of evaporites from adjacent salt domes has little impact on present formation water composition. Geochemical simulations with Harvie-M{phi}ller-Weare and PHRQPITZ thermodynamic data sets suggest secondary fluid enrichment in Ca, HCO{sub 3} and Sr by water-rock interaction. The volumetric mass balance between Ca enrichment and Mg depletion confirms dolomitization as the major alteration process. Potassium/Cl ratios below evaporation trajectory are attributed to minor precipitation of K feldspar and illitization without evidence for albitization at the Jujo-Tecominoacan reservoir. The abundance of secondary dolomite, illite and pyrite in drilling cores from reservoir host rock reconfirms the observed water-rock exchange processes. Sulfate concentrations are controlled by anhydrite solubility as indicated by positive SI-values, although anhydrite deposition is limited throughout the lithological reservoir column. The chemical variety of produced water at the Jujo-Tecominoacan oil field is related to a sequence of primary and secondary processes, including infiltration of evaporated seawater and original meteoric fluids, the subsequent

  13. Geochronology of the Palaeoproterozoic Kautokeino Greenstone Belt, Finnmark, Norway, in its Fennoscandian context (United States)

    Bingen, Bernard; Solli, Arne; Viola, Giulio; Sverre Sandstad, Jan; Torgersen, Espen; Whitehouse, Martin J.; Skår, Øyvind; Nasuti, Aziz


    The northeastern part of the Fennoscandian Shield consists of Archaean cratonic blocks alternating with Palaeoproterozoic greenstone belts ranging in age from c. 2500 to 1950 Ma. Traditionally, the greenstones are interpeted as evidence for rifting of the Archaean continent(s) although it remains unclear whether modern-style oceanic lithosphere developed, followed by a Wilson-cycle-type closure during the Svecokarelian orogeny. Existing geological, isotopic and geochronological data show that the exposed basins hosting the greenstones have distinct lithostratigraphies and geological evolutions and are pericontinental rather than oceanic. A diversity of Palaeoproterozoic mafic mantle derived magmatic rocks show a secular increase of Nd value with time, from EpsilonNd =-2 at 2500 Ma (Shalskiy dikes, Onega, Russia) to EpsilonNd =+4.4 at 2090 Ma (Jouttiaapa basalts, Peräpohja, Finland), suggesting that the regional asthenospheric mantle was less depleted than the model MORB-producing depleted mantle before 2090 Ma. In this work, we report new zircon U-Pb geochronological data in 19 samples from Finnmarkvidda, Norway, to constrain the evolution of the Palaeoproterozoic high-strain Kautokeino Greenstone Belt and its relations with the neighbouring felsic Jergul and Ráiseatnu gneiss complexes. The Jergul complex is an Archaean, low heat flow, TTG cratonic bloc of Karelian affinity formed between 2975 ±10 and 2776 ±6 Ma. The Masi formation, at the base of the Kautokeino Greenstone Belt, is a typical Jatulian quartzite unconformably overlying the Archean basement. An albite-magnetite-rich mafic sill, similar to the Haaskalehto intrusion in Finland, provides a minimum age of 2220 ±7 Ma for the deposition of the quartzite. The Likčá and Čáskejas formations represent the main basaltic volcanism. Direct evidence of an oceanic setting or oceanic suture is lacking. A probably synvolcanic gabbro sill gives an age of 2137 ±5 Ma. Published Sm-Nd whole-rock data on

  14. Geochemical Charactristics and Genesis of Topaz—Bearing Porphyries in Yangbin Area of Taishun County,Zhejiang Province

    Institute of Scientific and Technical Information of China (English)

    王德滋; 刘昌实; 等


    The host rocks of the porphyry tin deposits in the Yangbin area are prince-pally topaz-bearing porphyry dikes about 2 km long and 2-20m wide.Three lithologic types are identified for the dikes:topaz-bearing potassium feldspar granitic porphyry,topaz-bearing monzonitic granitic porphyry and topaz-bearing quartz porphyry.The con-tent of topaz in the rocks ranges from 10 to 20 vol.%.Porphyritic texture is characteristic,with quartz,potassium feldspar and albite as main phenocryst minerals.The phenocryst occupies 10-20vol% of the rocks.The rock groundmass consists of subhedrak topaz,quartz and protolithionite.Topaz has a unit-cell parameter b=8.797(A)°,and F:OH=1.92:0.18, indicating a F-rich variety formed at high temperature .The topaz-bearing porphyries occurring in this area are strongly peraluminous (A/NKC=1.574-12.94),with high ra-tios of F/C1(146-303) and Rb/Sr(5-122).They are rich in incompatible elements (Sn,313×10-6-1042×10-6;W,6×10-6-218×10-6;Nb,27×10-6-54×10-6),but poor in compatible elements (Sr,10×10-6-28×10-6;Ba,58×10-6-73×10-6;V,3×10-6-10×10-6,Cl,150×10-6-226×10-6).The rocks are also characterized by high total REE amount (281.69×10-6-319.76×10-6);with strong Eu depletion (&Eu=0.01-0.03)and low ratio of LREE/HREE(0.78-0.84).In summary ,the authors propose propose an idea of S-type genesis for the topaz-bearing porphyries with tin mineralization,instead of I-type.

  15. Diagenesis and reservoir quality evolution of palaeocene deep-water, marine sandstones, the Shetland-Faroes Basin, British continental shelf

    Energy Technology Data Exchange (ETDEWEB)

    Mansurbeg, H. [Department of Earth Sciences, Uppsala University, Villavaegen 16, SE 752 36 Uppsala (Sweden); Morad, S. [Department of Earth Sciences, Uppsala University, Villavaegen 16, SE 752 36 Uppsala (Sweden); Department of Petroleum Geosciences, The Petroleum Institute, P.O. Box 2533, Abu Dhabi (United Arab Emirates); Salem, A. [Faculty of Education at Kafr El-Sheikh, Tanta University, Kafr El-Sheikh (Egypt); Marfil, R.; Caja, M.A. [Departmento Petrologia y Geoquimica, Facultad de Geologia, UCM, 28040 Madrid (Spain); El-ghali, M.A.K. (Geology Department, Al-Fateh University, P.O. Box 13696, Libya); Nystuen, J.P. [Department of Geosciences, University of Oslo, P.O. Box 1047 Blindern, NO-0316 Oslo (Norway); Amorosi, A. [Department of Earth Sciences, University of Bologna, Via Zamboni 67, 40127 Bologna (Italy); Garcia, D. [Centre SPIN, Department GENERIC, Ecole Nationale Superieure des Mines de Saint Etienne 158, Cours Fauriel 42023, Saint-Etienne (France); La Iglesia, A. [Instituto de Geologia Economica (CSIC-UCM), Facultad de Geologia, UCM, 28040 Madrid (Spain)


    eogenetic kaolinite, smectite and mesogenetic illite and chlorite. Kaolinite has been subjected to mesogenetic replacement by dickite. The K-feldspar and plagioclase grains have been albitized. Dissolution of calcite cement and of framework grain (feldspar, volcanic fragments and mud intraclasts) has resulted in a considerable enhancement of reservoir quality. (author)

  16. Abiotic degradation rates for carbon tetrachloride and chloroform: Final report.

    Energy Technology Data Exchange (ETDEWEB)

    Amonette, James E.; Jeffers, Peter M.; Qafoku, Odeta; Russell, Colleen K.; Humphrys, Daniel R.; Wietsma, Thomas W.; Truex, Michael J.


    This report documents the objectives, technical approach, and progress made through FY 2012 on a project initiated in FY 2006 to help address uncertainties related to the rates of hydrolysis in groundwater for carbon tetrachloride (CT) and chloroform (CF). The project also sought to explore the possible effects of contact with minerals and sediment (i.e., heterogeneous hydrolysis) on these rates. We conducted 114 hydrolysis rate experiments in sealed vessels across a temperature range of 20-93 °C for periods as long as 6 years, and used the Arrhenius equation to estimate activation energies and calculate half-lives for typical Hanford groundwater conditions (temperature of 16 °C and pH of 7.75). We calculated a half-life of 630 years for hydrolysis for CT under these conditions and found that CT hydrolysis was unaffected by contact with sterilized, oxidized minerals or Hanford sediment within the sensitivity of our experiments. In contrast to CT, hydrolysis of CF was generally slower and very sensitive to pH due to the presence of both neutral and base-catalyzed hydrolysis pathways. We calculated a half-life of 3400 years for hydrolysis of CF in homogeneous solution at 16 °C and pH 7.75. Experiments in suspensions of Hanford sediment or smectite, the dominant clay mineral in Hanford sediment, equilibrated to an initial pH of 7.2, yielded calculated half-lives of 1700 years and 190 years, respectively, at 16 °C. Experiments with three other mineral phases at the same pH (muscovite mica, albite feldspar, and kaolinite) showed no change from the homogeneous solution results (i.e., a half-life of 3400 years). The strong influence of Hanford sediment on CF hydrolysis was attributed to the presence of smectite and its ability to adsorb protons, thereby buffering the solution pH at a higher level than would otherwise occur. The project also determined liquid-vapor partition coefficients for CT under the temperatures and pressures encountered in the sealed vessels that

  17. Physical, Chemical and Mineral Properties of the Polonnaruwa Stones (United States)

    Wallis, Jamie; Wickramasinghe, N. C.; Wallis, Daryl H.; Miyake, Nori; Wallis, M. K.; Hoover, Richard B.; Samaranayake, Anil; Wickramarathne, Keerthi; Oldroyd, Anthony

    We report on the physical, chemical and mineral properties of a series of stone fragments recovered from the North Central Province of Sri Lanka following a witnessed fireball event on 29 December 2012. The stones exhibit highly porous poikilitic textures comprising of isotropic silica-rich/plagioclase-like hosts. Inclusions range in size and shape from mm-sized to smaller subangular grains frequently more fractured than the surrounding host and include ilmenite, olivine (fayalitic), quartz and accessory zircon. Bulk mineral compositions include accessory cristobalite, hercynite, anorthite, wuestite, albite, anorthoclase and the high pressure olivine polymorph wadsleyite, suggesting previous endurance of a shock pressure of ~20GPa. Further evidence of shock is confirmed by theconversion of all plagioclase to maskelynite. Here the infrared absorption spectra in the region 580 cm-1 to 380 cm-1 due to the Si-O-Si or Si-O-Al absorption band shows a partial shift in the peak at 380 cm-1 towards 480 cm-1 indicating an intermediate position between crystalline and amorphous phase. Host matrix chemical compositions vary between samples, but all are rich in SiO2. Silica-rich melts display a heterogeneous K-enrichment comparable to that reported in a range of nonterrestrial material from rare iron meteorites to LL chondritic breccias and Lunar granites. Bulk chemical compositions of plagioclase-like samples are comparable to reported data e.g. Miller Ranger 05035 (Lunar), while Si-rich samples accord well with mafic and felsic glasses reported in NWA 1664 (Howardite)as well asdata for fusion crust present in a variety of meteoritic samples.Triple oxygen isotope results show Δ17O = .0.335 with δ18O (‰ rel. SMOW) values of 17.816 ± 0.100 and compare well with those of known CI chondrites and are within the range of CI-like (Meta-C) chondrites. Rare earth elemental abundances show a profound Europium anomaly of between 0.7 and 0.9 ppm while CI normalized REE patterns

  18. Evidence of unadulterated mantle-depth, granitic melt inclusions: kumdykolite and kokchetavite crystallized from melt in Bohemian Massif granulites. (United States)

    O´Brien, Patrick J.; Ferrero, Silvio; Ziemann, Martin A.; Walczak, Katarzyna; Wunder, Bernd; Hecht, Lutz; Wälle, Markus


    Partial melting under near-UHP conditions of metagranitoids (now HP felsic granulites) at mantle depth in the Orlica-Śnieżnik Dome (Bohemian Massif, Poland) is recorded in small volumes of hydrous melt trapped as primary melt inclusions (MI) in peritectic garnets. When free of cracks connecting the inclusion with the leucocratic matrix, these "nanogranites" (≤ 50μm inclusion diameter) contain a unique assemblage including kumdykolite, kokchetavite and cristobalite - polymorphs of albite, K-feldspar and quartz, respectively. These usually metastable phases crystallized from the melt (glass?) during rapid exhumation (cm/a) at high T but the crack-free state strongly suggests over-pressuring of the inclusion with respect to the pressure-time path followed by the matrix. Reports of both kumdykolite and kokchetavite have been mainly from natural rocks equilibrated in the diamond stability field. The precise calculation of the PT path of the MI on cooling and the comparison with previous studies suggests, however, that pressure is not influential to their formation, ruling out the possible interpretation of kumdykolite and kokchetavite as indicators of ultra-high pressure conditions. Experimental re-homogenization of these crack-free nanogranites was achieved using a piston cylinder apparatus at 2.7 GPa and 875°C. These conditions are consistent with the results of geothermobarometric calculations on the host rock, suggesting that no H2O loss occurred during exhumation as this would have caused a shift of the inclusion melting T toward higher values. Coupled with the absence of H2O-loss microstructural evidence, e.g. decrepitation cracks and/or vesciculation in re-homogenized nanogranites, this evidence suggests that the nanogranites still preserve the original H2O content of the melt. Both experimental and microstructural evidence support the hypothesis that the presence of these polymorphs should be regarded as direct mineralogical criterion to identify former

  19. Geology and geochemistry of the shear-hosted Julie gold deposit, NW Ghana (United States)

    Amponsah, Prince Ofori; Salvi, Stefano; Béziat, Didier; Siebenaller, Luc; Baratoux, Lenka; Jessell, Mark W.


    The Leo Man Craton in West Africa is host to numerous economic gold deposits. If some regions, such as the SW of Ghana, are well known for world-class mineralizations and have been extensively studied, gold occurrences elsewhere in the craton have been discovered only in the last half a century or so, and very little is known about them. The Julie gold deposit, located in the Paleoproterozoic Birimian terrane of NW Ghana, is one such case. This deposit is hosted in a series of granitoid intrusives of TTG composition, and consists of a network of deformed, boudinaged quartz lodes (A-type veins) contained within an early DJ1 E-W trending shear zone with dextral characteristics. A conjugate set of veins (C-type) perpendicular to the A-type veins contains low grade mineralization. The main ore zone defines a lenticular corridor about 20-50 m in width and about 3.5 km along strike, trending E-W and dipping between 30 and 60°N. The corridor is strongly altered, by an assemblage of sericite + quartz + ankerite + calcite + tourmaline + pyrite. This is surrounded by a second alteration assemblage, consisting of albite + sericite + calcite + chlorite + pyrite + rutile, which marks a lateral alteration that fades into the unaltered rock. Mass balance calculations show that during alteration overall mass was conserved and elemental transfer is generally consistent with sulfidation, sericitization and carbonatization of the host TTG. Gold is closely associated with pyrite, which occurs as disseminated grains in the veins and in the host rock, within the mineralized corridor. SEM imagery and LA-ICP-MS analyses of pyrites indicate that in A-type veins gold is associated with bismuth, tellurium, lead and silver, while in C-type veins it is mostly associated with silver. Pyrites in A-type veins contain gold as inclusions and as free gold on its edges and fractures, while pyrites from C-type veins contains mostly free gold. Primary and pseudosecondary fluid inclusions from both

  20. Pressure conditions for the solidification of the Skaergaard intrusion: Eruption of East Greenland flood basalts in less than 300,000 years (United States)

    Larsen, Rune B.; Tegner, Christian


    Primary granophyres are differentiated from olivine tholeiitic magma and occur interstitially throughout the cumulus stratigraphy of the Skaergaard intrusion, East Greenland. Samples from the Lower Zones a-c (LZa-c), the Middle Zone (MZ) and the Sandwich Horizon (SH) are included in the present study together with granophyric accumulations in gabbroic pegmatite from LZa-c. Fluid inclusions in quartz and the mineral assemblage in the granophyres record the pressure under which the Skaergaard intrusion crystallised. Pegmatitic granophyre from LZa-c consists mainly of quartz, plagioclase (An 4-7) and alkali feldspar (Or 40-80) enclosing an earlier formed assemblage of ferrohastingsitic and ferroedenitic hornblende, fayalite (Fo 4-5), titanite, biotite and fluor-apatite. Granophyric quartz, albite and alkali feldspar crystallised from water-saturated granitic melts near eutectic minimum conditions between 680 and 660 °C. The pressure of granophyre crystallisation was modelled by the intercept between fluid inclusion isochores and the minimum melt solidus for granitic compositions. Pressures, recalculated to the roof pendant of the intrusion, are 0.7 ± 0.5 for LZa, 2.0 ± 0.2 for LZb-c, 2.3 ± 0.8 for MZ (the Triple Group level) and 3.3 ± 1.3 kb for SH. Amphibole geobarometry, independently, confirm the pressure estimates for pegmatitic granophyres in LZa-c. The granophyres formed as the intrusion cooled through the minimum melt solidus in LZa, LZb, LZc, MZ and SH, respectively. The pressure increase from LZa to SH granophyres is explained by progressive burial during cooling of the intrusion and contemporaneous outpouring of 5.3-6.3 ± 2.7 km of flood basalts during the initial opening of the Northeast Atlantic Ocean. Accordingly, the Skaergaard intrusion evolved from a subvolcanic magma chamber at emplacement to a more deep-seated igneous system during terminal crystallization when the majority of the intercumulus phases formed. The present cooling history suggests

  1. Liquids of the Skaergaard intrusion traced by melt inclusions (United States)

    Jakobsen, J. K.; Veksler, I. V.; Tegner, C.


    The Skaergaard intrusion, East Greenland, has for the past 75 years played a central role in the understanding of differentiation of tholeiitic magma. However, there is still no agreement on the general line of liquid descent. Here we compile the inference from melt inclusion in cumulus apatite and plagioclase as a direct tracer of the parental melt composition and its evolution. Compositions of crystallized melt inclusions have been estimated by broad beam analysis, mass balance summation and by remelting and homogenization. Melt inclusions in apatite are found in the Upper Zone and are of two types: One is dark brownish or opaque and contains finely crystallized daughter phases of plagioclase, ilmenite, magnetite, iron-rich biotite (lepidomelane) and a fine-grained matrix; a less abundant type is light-colored, transparent and consists of quartz, orthoclase, albite, minor magnetite and finely intergrown matrix. The predominant dark melt inclusions are extremely rich in FeOT (30.9 ± 4.2 wt%) and low in SiO2 (40.7 ± 3.6 wt%) whereas the light colored type contains 8.6 ± 5.9 wt% FeOT and 65.6 ± 7.3 wt% SiO2. The contrasting compositions is interpreted as entrapment of conjugate end-members of two immiscible liquids. Before apatite is saturated (Lower- and Middle Zone), melt inclusions in plagioclase represent the best available tracer of liquid compositions. The melt inclusions are fully crystallized and consist of a uniform daughter phase assemblage of highly variable modal proportions: plagioclase (42-59 %), clinopyroxene (29-41 %), ilmenite (6-9 %), magnetite (4-10%), apatite (1-9 %), and accessory phases (Skaergaard in the upper part of the Lower Zone close to the first appearance of liquidus magnetite and that the Upper Zone crystallized from an immiscible emulsion. The extent of gravitational separation of the two contrasting melts and macroscopic effects of unmixing on the Skaergaard magma remain, however, unclear. We expect to clarify these issues by

  2. Fluorapatite in carbonatite-related phosphate deposits: the case of the Matongo carbonatite (Burundi) (United States)

    Decrée, Sophie; Boulvais, Philippe; Tack, Luc; André, Luc; Baele, Jean-Marc


    The Matongo carbonatite intrusive body in the Neoproterozoic Upper Ruvubu alkaline plutonic complex (URAPC) in Burundi is overlain by an economic phosphate ore deposit that is present as breccia lenses. The ore exhibits evidence of supergene enrichment but also preserves textures related to the concentration of fluorapatite in the carbonatitic system. Magmatic fluorapatite is abundant in the ore and commonly occurs as millimeter-sized aggregates. It is enriched in light rare earth elements (LREE), which is especially apparent in the final generation of magmatic fluorapatite (up to 1.32 wt% LREE2O3). After an episode of metasomatism (fenitization), which led to the formation of K-feldspar and albite, the fluorapatite-rich rocks were partly brecciated. Oxygen and carbon isotope compositions obtained on the calcite forming the breccia matrix (δ18O = 22.1 ‰ and δ13C = -1.5 ‰) are consistent with the involvement of a fluid resulting from the mixing of magmatic-derived fluids with a metamorphic fluid originating from the country rocks. In a subsequent postmagmatic event, the carbonates hosting fluorapatite were dissolved, leading to intense brecciation of the fluorapatite-rich rocks. Secondary carbonate-fluorapatite (less enriched in LREE with 0.07-0.24 wt% LREE2O3 but locally associated with monazite) and coeval siderite constitute the matrix of these breccias. Siderite has δ18O values between 25.4 and 27.7 ‰ and very low δ13C values (from -12.4 to -9.2 ‰), which are consistent with the contribution of organic-derived low δ13C carbon from groundwater. These signatures emphasize supergene alteration. Finally, the remaining voids were filled with a LREE-poor fibrous fluorapatite (0.01 wt% LREE2O3), forming hardened phosphorite, still under supergene conditions. Pyrochlore and vanadiferous magnetite are other minerals accumulated in the eluvial horizons. As a consequence of the supergene processes and fluorapatite accumulation, the phosphate ore, which

  3. Strain localization in brittle-ductile shear zones: fluid abundant vs fluid limited conditions (an example from Wyangala area, Australia

    Directory of Open Access Journals (Sweden)

    L. Spruzeniece


    Full Text Available This study focuses on physiochemical processes occurring in a brittle-ductile shear zone at both fluid-present and fluid-limited conditions. In the studied shear zone (Wyangala, SE Australia, a coarse-grained two feldspar-quartz-biotite granite is transformed into a medium grained orthogneiss at the shear zone margins and a fine-grained quartz-muscovite phyllonite in the central parts. The orthogneiss displays cataclasis of feldspar and crystal-plastic deformation of quartz. Quartz accommodates most of the deformation and is extensively recrystallized showing distinct crystallographic preferred orientation (CPO. Feldspar-to-muscovite, biotite-to-muscovite and albitization reactions occur locally at porphyroclasts' fracture surfaces and margins. However, the bulk rock composition shows very little change in respect to the wall rock composition. In contrast, in the shear zone centre quartz occurs as large, weakly deformed porphyroclasts, in sizes similar to that in the wall rock, suggesting that it has undergone little deformation. Feldspars and biotite are almost completely reacted to muscovite, which is arranged in a fine-grained interconnected matrix. Muscovite-rich layers contain significant amounts of fine-grained intermixed quartz with random CPO. These domains are interpreted to have accommodated most of the strain. Bulk rock chemistry data shows a significant increase in SiO2 and depletion in NaO content compared to the wall rock composition. We suggest that the high and low strain fabrics represent markedly different scenarios and cannot be interpreted as a simple sequential development with respect to strain. We suggest that the fabrics and mineralogical changes in the shear zone centre have formed due to fluid influx probably along an initially brittle fracture. Here, hydration reactions dramatically changed the rheological properties of the rock. In the newly produced muscovite-quartz layers creep cavitation associated with grain

  4. Untangling Element Fluxes From The Subducting Slabs: Aqueous Solutions Through The Electrostatic Lense (United States)

    Galvez, M.; Connolly, J. A.; Manning, C. E.


    Understanding the deep cycling of elements hinges on characterizing the chemistry of fluids in subduction zones. Aqueous solutions dielectric properties determine their characteristics as solvents for rocks. Predicting the composition and speciation of fluid solutions at equilibrium with complex mineral assemblages has been a long lasting challenge. We have developed a model to explore the composition and speciation of metamorphic aqueous solutions to upper mantle pressure and temperature. Our model combines Gibbs free energy minimization of rock and molecular fluids with an electrostatic approach to describe solute-solute and solute-solvent interactions in the fluid phase. Using an extension of the Debye-Onsager-Kirkwood model to characterize the dielectric properties of COH solutions, we derive aqueous fluid speciation by solving the mass action and charge balance of the system. This framework is applied to various slab lithologies. We find, e.g., that the pH of carbonated basalts and pelites is alkaline, i.e. ~2-2.5 pH units above neutrality, in C and Cl-free fluids and shows an isothermal decrease above the albite-jadeite-quartz equilibrium, at P ~ 2 GPa. C and Chlorine (1M) decrease the alkalinity by a combined ~ 1.5 pH unit, with variations tied to the thermal structure and mineral assemblages along typical P-T paths. The results produced are compared with experimental solubility measurements on identical systems. Significant discrepancies reveal that the process of solute polymerization at elevated T and P is more general than previously recognized. Unaccounted species contain, in addition to Na, Si and Al, an important fraction of the total dissolved load of the elements K, Ca and Mg (>50% at T= 600 °C and P = 2 Ga). Finally, we show that knowledge of the acid-base properties of metamorphic fluid solutions affect the (de)coupling between C and alkali-earth mobility, and magnitude of low-T C transfers associated to carbonate dissolution through time. This

  5. Brittle deformation in Southern Granulite Terrane (SGT): A study of pseudotachylyte bearing fractures along Gangavalli Shear Zone (GSZ), Tamil Nadu, India. (United States)

    mohan Behera, Bhuban; Thirukumaran, Venugopal; Biswal, Tapas kumar


    High grade metamorphism and intense deformation have given a well recognition to the Southern Granulite Terrane (SGT) in India. TTG-Charnockite and basic granulites constitute the dominant lithoassociation of the area. Dunite-peridotite-anorthosite-shonkinite and syenites are the intrusives. TTG-charnockite-basic granulite have undergone F1 (isoclinal recumbent), F2 (NE-SW) and F3 (NW-SE) folds producing several interference pattern. E-W trending Neoarchean and Palaeoproterozoic Salem-Attur Shear Zone exhibits a low angle ductile thrust as well as some foot print of late stage brittle deformation near Gangavalli area of Tamil Nadu. The thrust causes exhumation of basic granulites to upper crust. Thrusting along the decollement has retrograded the granulite into amphibolite rock. Subsequently, deformation pattern of Gangavalli area has distinctly marked by numerous vertical to sub-vertical fractures mostly dominating along 0-15 and 270-300 degree within charnockite hills that creates a maximum stress (σ1) along NNW and minimum stress (σ3) along ENE. However, emplacement of pseudotachylyte vein along N-S dominating fracture indicates a post deformational seismic event. Extensive fractures produce anastomose vein with varying thickness from few millimeters to 10 centimeters on the outcrop. ICP-AES study results an isochemical composition of pseudotachylyte vein that derived from the host charnockitic rock where it occurs. But still some noticeable variation in FeO-MgO and Na2O-CaO are obtained from different parts within the single vein showing heterogeneity melt. Electron probe micro analysis of thin sections reveals the existence of melt immiscibility during its solidification. Under dry melting condition, albitic rich melts are considered to be the most favorable composition for microlites (e.g. sheaf and acicular micro crystal) re-crystallization. Especially, acicular microlites preserved tachylite texture that suggest its formation before the final coagulation

  6. Seismic slip at the base of the seismogenic layer along the exhumed extensional Oligocene Trois Villes Fault (Western Italian Alps) (United States)

    Bistacchi, A.; Gatta, D.; Grizzetti, R.; Pennacchioni, G.


    The characterisation of fault rocks from exhumed faults is of paramount importance in fault and earthquake mechanics, since these rocks might provide constraints for models of seismic rupture initiation and propagation. The Trois Ville Fault is a major Oligocene extensional fault of the internal NW Alps, showing a cumulative displacement of c.a. 1 km evidenced by the offset boundary between Austroalpine gneisses (hangingwall) and Piedmont calcschists (footwall). Fault rocks consist of greenschist mylonitic gneiss (from an early stage), green indurated cataclasites, which constitute the 2-10 m thick core zone, and a thin (c.a. 10 cm) but extremely continuous layer of polycyclic pseudotachylytes which mark a strongly localised principal slipping zone. Pseudotachylytes lack distinctive features such as glass, microlites-spherulites, etc., but show a distinctive mineralogy of the melt-derived very fine-grained matrix, which is almost entirely constituted by monoclinic K-feldspar (low sanidine crystallised at ca. 990°C and partly ordered as far as 500- 700°C). This matrix is composed by very small crystals (0.5-5 μm), organised in aggregates and dendritic snowflake-like aggregates which might be explained by sintering or synneusis processes. The high crystallization T implies that pseudotachylytes derive from frictional melting of ultracataclasites (possibly incoherent, hence a fault gouge, at the time of deformation) near the brittle plastic transition (250- 300°C and 8-10 km). Hence, a new diagnostic criterion for frictional melting, based on crystallographic analysis, is introduced in this work. The melt mainly derived from phyllosilicates (muscovite and minor chlorite; Tmelt c.a. 750°C) and evidences of superheating may be envisaged (partial assimilation of albite and quartz; T > c.a. 1300°C). This points to a considerable seismic slip after the onset of frictional melting and to an efficient melting lubrication process in this kind of fault rocks

  7. Caracterización geoquímica y estudio comparativo de plagiogranitos de las Zonas Surportuguesa y Ossa-Morena (SO del Macizo Ibérico, España

    Directory of Open Access Journals (Sweden)

    Bellido, F.


    Full Text Available Plagiogranites and albitic rocks belonging to contrasted magmatic associations of different ages and geodynamic environments outcrop in Ossa-Morena (OMZ and Surportuguese (SPZ Zones. OMZ plagiogranites are related with Cambrian-Ordovician rifting and represent a part of the felsic members of a bimodal magmatic suite and show oceanic plagiogranites affinities. SPZ plagiogranites are related with a Carboniferous volcano-plutonic calc-alkaline suite related with Variscan Orogeny. Both plagiogranites show many similar petrological and geochemical characteristics but display some different immobile elements ratios as La/Nb, Th/Nb, Th/La that are unaltered by metamorphism, magmatic differentiation and alteration processes and prove differences in their sources. SPZ plagiogranites show a more compositional homogeneity than OMZ ones. This is interpreted as a proof of cogenetic origin for SPZ plagiogranites and heterogeneous origin for OMZ plagiogranites, derived from the mix of different sources (astenospheric, lithospheric and crustal.

    En la Zona de Ossa-Morena (ZOM y en la Zona Surportuguesa (ZSP se encuentran plagiogranitos pertenecientes a asociaciones magmáticas y ambientes geodinámicos muy contrastados. Los primeros pertenecen a una asociación bimodal máfica-félsica relacionada con el rifting cámbrico-ordovícico y presentan bastantes afinidades con plagiogranitos oceánicos. Los segundos forman parte de una asociación volcánico-plutónica calcoalcalina carbonífera relacionada con la Orogenia Varisca. Ambos plagio-granitos son semejantes en diversos aspectos petrológicos y geoquímicos pero muestran diferencias en algunas relaciones de elementos inmóviles tales como La/Nb, Th/Nb, Th/La poco sensibles a los procesos de evolución magmática, metamorfismo y alteración y que son reflejo de la composición de las fuentes. Los plagiogranitos de la ZSP presentan una mayor homogeneidad composicional que los de la ZOM. Esto se

  8. Kuh-e Dom Fe-Cu-Au prospect, Anarak Metallogenic Complex, Central Iran: a geological, mineralogical and fluid inclusion study (United States)

    Tale Fazel, Ebrahim; Mehrabi, Behzad; Tabbakh Shabani, Amir Ali


    The Kuh-e Dom Fe-Cu-Au prospect is located in the Urumieh-Dokhtar Magmatic Belt, and is characterized by copper-iron oxide and gold veins, stockworks and breccias hosted by the Eocene Kuh-e Dom arc intrusion. Mineralization is located within NE-SW to WNW-ESE sinistral faults and likely formed in a subduction-related continental margin that is typical of IOCG deposit systems. The deposits have a distinct metal composition of Fe, Cu, Bi, Co, Mo and LREE with gold (up to 3 g/t), and the mineral assemblages are quartz, hematite, pyrite, chalcopyrite, emplectite, magnetite, free gold, calcite, barite, chlorite, and tourmaline. Three paragenetic stages of mineralized quartz veins are distinguished in the Kuh-e Dom prospect, including: (i) hematite-bearing quartz veins, (ii) quartz-sulfide stockwork and breccia veins, and (iii) quartz-calcite±sulfide infilling veins. Sodic (albitization), potassic, and quartz-calcite±chlorite pervasive alterations are commonly associated with these three mineralization stages. Three types of fluid inclusions have been identified at Kuh-e Dom, including: aqueous two-phase (H2O-NaCl-CaCl2±FeCl2), halite-saturated aqueous (H2O-NaCl±KCl), and CO2-bearing (H2O-CO2±CH4 and CO2±CH4) fluid inclusions. A hypersaline (~35 wt% NaCl equiv.), aqueous magmatic fluid was released at about 400 °C and a pressure of nearly 4 kbar, forming early hematite-bearing quartz veins. These high salinity fluids were progressively diluted further away from Kuh-e Dom intrusion due to substantial input of meteoric water and mixing with the magmatic components during the middle and late stages of mineralization. The mineralogy, alteration, and fluid composition of the Kuh-e Dom Fe-Cu-Au prospect compared well with Fe oxide Cu-Au (IOCG) deposits worldwide.

  9. U-Pb zircon and biostratigraphic data of high-pressure/low-temperature metamorphic rocks of the Talea Ori: tracking the Paleotethys suture in central Crete, Greece (United States)

    Zulauf, G.; Dörr, W.; Krahl, J.; Lahaye, Y.; Chatzaras, V.; Xypolias, P.


    Inherited deformation microfabrics of detrital quartz grains and U-Pb (Laser ablation (LA)-ICPMS and ID TIMS) ages of detrital zircons separated from the Phyllite-Quartzite Unit s.l. of the Talea Ori, central Crete, suggest strikingly different source rocks. Albite gneiss of the lower Rogdia Beds includes Cambrian and Neoproterozoic rounded zircons with main U-Pb age peaks at 628 and 988 Ma. These and minor Paleoproterozoic and Archean peaks, together with the lack of Variscan-aged and Mesoproterozoic zircons, are similar to the age spectra obtained from the Phyllite-Quartzite Unit s.str. of the Peloponnesus and eastern Crete and from the Taurides. All of these zircons should be derived from the northeastern passive margin of Gondwana (Cimmeria). Metatuffites of the uppermost Rogdia Beds and metasandstone of Bali beach, on the other hand, include euhedral detrital zircons displaying a Variscan U-Pb age spectra at ca. 300 Ma with concordia ages at 291 ± 3, 300 ± 1 Ma (Rogdia) and 286 ± 3, 300 ± 3, 313 ± 2 Ma (Bali). Both types of metasediments and their zircons are similar to those of the pre-Alpine basement and overlying Tyros Beds of eastern Crete, revealing a provenance at the southern active margin of Laurasia. Thus, in central Crete the Paleotethys suture should be situated inside the Rogdia Beds. Magmatic zircons separated from a rhyolite boulder of the lower Achlada Beds yielded a concordant U-Pb zircon age at 242 ± 2 Ma placing a maximum age for the deposition of the (meta)conglomerate from which the boulder was collected. This age is compatible with an Olenekian-early Anisian age of the underlying Vasilikon marble suggested by new findings of the foraminifera Meandrospira aff. pusilla. Both the Achlada Beds and the Vasilikon marble can be attributed to the lower Tyros Beds of eastern Crete. The Alpine deformation led to a pervasive mylonitic foliation, which is affecting most of the studied rocks. This foliation results from D2 top

  10. Formation Water Geochemistry and Its Controlling Factors: Case Study on Shiwu Rifted Sub-basin of Songliao Basin, NE China

    Institute of Scientific and Technical Information of China (English)


    A common way to trace fluid flow and hydrocarbon accumulation is by studying the geochemistry of formation water. This paper focuses on the spacial distribution of the geochemical features of the formation water in the Shiwu Rifted Basin and its indication of the water-rock interaction processes. The hydrodynamic field controls the spacial distribution of formation water. Due to the penetration of meteoric water, the salinity is below 4,500mg/L at the basin margin and the severely faulted central ridge and increases basin ward to 7,000-10,000mg/L. The vertical change of formation water can be divided into 3 zones, which correspond respectively to the free replacement zone (<1,250m), the obstructed replacement zone (1,250m-1,650m) and thelagged zone (>1,650m) in hydrodynamics. In the free replacement zone, the formation water is NaHCO3-type with its salinity increased to 10,000mg/L. The formation water in the obstructed replacement zone is Na2SO4-type with its salinity decreased to 5,000mg/L-7,000mg/L because of the dehydration of mud rocks. The formation water in the lagged zone is CaCl2-type, but its salinity decreases sharply at a depth of 1,650m and then increases vertically downward to 10,000mg/L. This phenomenon can be best explained by the osmosis effect rather than the dehydration of mud rocks. The relationships between Cl--HCO3- and Na++K+-Ca2+ show that the initial water-rock interaction is the dissolution of NaCl and calcium-bearing carbonate, causing an increase of Na+-K+-Ca2+-Cl- and salinity. The succeeding water-rock interaction is albitization, which leads to a decrease of Na+ and an increase of Ca2+ simultaneously, and generates CaCl2-type fluid. The above analysis shows that the geochemical evolution of formation water is governed by the water-rock interactions, while its spacial distribution is controlled by the hydrological conditions. The water-rock interaction processes are supported by other geological observations, suggesting that

  11. Re-equilibration history and P- T path of eclogites from Variscan Sardinia, Italy: a case study from the medium-grade metamorphic complex (United States)

    Cruciani, Gabriele; Franceschelli, Marcello; Groppo, Chiara; Oggiano, Giacomo; Spano, Maria Elena


    Retrogressed eclogites are hosted within the Variscan low- to medium-grade metamorphic complex near Giuncana, north-central Sardinia. These rocks are medium to fine grained with garnet and amphibole as the most abundant mineral phases along with clinopyroxene, plagioclase, quartz, biotite, chlorite, epidote, ilmenite, rutile and titanite. Four stages of mineralogical re-equilibration have been distinguished. The stage I is characterized by the occurrence of omphacite, epidote, quartz, amphibole, rutile and ilmenite in garnet poikiloblasts. The stage II is characterized by two types of symplectitic microstructures: (1) amphibole + quartz symplectite and (2) clinopyroxene + plagioclase ± amphibole symplectite. The first symplectite type replaces omphacite included in garnet, whereas the second one is widespread in the matrix. Biotite droplets and/or lamellae intimately growing with fine-grained plagioclase resemble biotite + plagioclase symplectite after phengite. The stage III is characterized by the widespread formation of amphibole: (1) as zoned porphyroblasts in the matrix, (2) as corona-type microstructure replacing garnet. Subordinate plagioclase (oligoclase) is also present in the amphibole corona. The stage IV is characterized by the local formation of biotite replacing garnet, actinolite, chlorite, albite and titanite. P- T pseudosections calculated with Perple_X give P- T conditions 580 < T < 660 °C, 1.3 < P < 1.8 GPa for the stage I. After the stage I, pressure decrease and temperature increase led to the breakdown of omphacite with the formation of clinopyroxene + plagioclase ± amphibole symplectite at ~1.25-1.40 GPa and 650-710 °C (stage II). P- T conditions of the amphibolite-facies stage III have been defined at 600-670 °C, P = 0.65-0.95 GPa. P- T conditions of the latest stage IV are in the range of greenschist facies. The P- T path of the retrogressed eclogite hosted in the medium-grade micaschist and paragneiss of Giuncana recalls the P- T

  12. Geochemistry and mineralogy of the Late Permian coals from the Songzao Coalfield, Chongqing,southwestern China

    Institute of Scientific and Technical Information of China (English)

    DAI ShiFeng; ZHOU YiPing; REN DeYi; WANG XiBo; LI Dan; ZHAO Lei


    Mineralogy and geochemistry of the four main workable coal seams (No.6, No.7, No.8, and No.11) of Late Permian age from the Songzao Coalfield, Chongqing, Southwest China, were examined using inductively coupled plasma-mass spectrometry (ICP-MS), X-ray fluorescence spectrometry (XRF),cold-vapor absorption spectrometry (CV-AAS), ion-selective electrode (ISE), scanning electron microscopy equipped with an energy-dispersive X-ray spectrometer (SEM-EDX), and X-ray diffraction analysis (XRD). The results showed that the main workable No.8 Coal that accounts for about 60% of the total coal reserves in the Songzao Coalfield was not enriched in hazardous trace elements. The No.11 Coal has high concentrations of alkaline elements, Be (9.14 μg/g), SC (12.9 μg/g), Ti (9508 μg/g),Mn (397 μg/g), Co (23.7 μg/g), Cu (108 μg/g), Zn (123 μg/g), Ga (32 μg/g), Zr (1304 μg/g), Nb (169 μg/g), Hf (32.7 μg/g), Ta (11.4 μg/g), W (24.8 μg/g), Hg (0.28 μg/g), Pb (28.1 μg/g), Th (24.1 μg/g), and rare earth elements (509.62 μg/g). The concentration of Nb and Ta in the No. 11 Coal is higher than the industrial grade, and their potential utilization should be further studied. Besides pyrite, quartz, calcite, and clay minerals, trace minerals including chalcopyrite, marcasite, siderite, albite, mixed-layer clay minerals of illite and smectite, monazite, apatite, anatase, chlorite, and gypsum were found in the No.11 Coal. It should be noted that alabandite of hydrothermal origin and anatase occurring as cement were identified in coal. In addition, the clayey microbands derived from alkaline volcanic ashes were identified in the coal. The dominant compositions of these clayey microbands were mixed-layer clay minerals of illite and smectite, which were interlayered with organic bands. The modes of occurrence of alkaline volcanic ash bands indicate that the volcanic activities were characterized by the multiple eruptions,short time interval and small scale for each eruption during

  13. Geochemistry and mineralogy of the Late Permian coals from the Songzao Coalfield, Chongqing,southwestern China

    Institute of Scientific and Technical Information of China (English)


    Mineralogy and geochemistry of the four main workable coal seams (No.6, No.7, No.8, and No.11) of Late Permian age from the Songzao Coalfield, Chongqing, Southwest China, were examined using in- ductively coupled plasma-mass spectrometry (ICP-MS), X-ray fluorescence spectrometry (XRF), cold-vapor absorption spectrometry (CV-AAS), ion-selective electrode (ISE), scanning electron mi- croscopy equipped with an energy-dispersive X-ray spectrometer (SEM-EDX), and X-ray diffraction analysis (XRD). The results showed that the main workable No.8 Coal that accounts for about 60% of the total coal reserves in the Songzao Coalfield was not enriched in hazardous trace elements. The No.11 Coal has high concentrations of alkaline elements, Be (9.14 μg/g), Sc (12.9 μg/g), Ti (9508 μg/g), Mn (397 μg/g), Co (23.7 μg/g), Cu (108 μg/g), Zn (123 μg/g), Ga (32 μg/g), Zr (1304 μg/g), Nb (169 μg/g), Hf (32.7 μg/g), Ta (11.4 μg/g), W (24.8 μg/g), Hg (0.28 μg/g), Pb (28.1 μg/g), Th (24.1 μg/g), and rare earth elements (509.62 μg/g). The concentration of Nb and Ta in the No. 11 Coal is higher than the industrial grade, and their potential utilization should be further studied. Besides pyrite, quartz, calcite, and clay minerals, trace minerals including chalcopyrite, marcasite, siderite, albite, mixed-layer clay minerals of illite and smectite, monazite, apatite, anatase, chlorite, and gypsum were found in the No.11 Coal. It should be noted that alabandite of hydrothermal origin and anatase occurring as cement were identi- fied in coal. In addition, the clayey microbands derived from alkaline volcanic ashes were identified in the coal. The dominant compositions of these clayey microbands were mixed-layer clay minerals of illite and smectite, which were interlayered with organic bands. The modes of occurrence of alkaline volcanic ash bands indicate that the volcanic activities were characterized by the multiple eruptions, short time interval and small scale for each eruption

  14. Neoproterozoic anorogenic magmatism in the Southern Bahia Alkaline Province of NE Brazil: U-Pb and Pb-Pb ages of the blue sodalite syenites (United States)

    Rosa, Maria de Lourdes da Silva; Conceição, Herbet; Macambira, Moacir José Buenano; Galarza, Marco Antonio; Cunha, Mônica Pringsheim; Menezes, Rita Cunha Leal; Marinho, Moacyr Moura; Filho, Basílio Elesbão da Cruz; Rios, Débora Correia


    Blue sodalite syenite is a rare rock, and the Southern Bahia Alkaline Province (SBAP) is the only place in Brazil where economic deposits are found. This province forms part of the Archaean to Paleoproterozoic São Francisco craton, and contains a few batholiths, a large number of stocks and hundreds of dykes. Its southern part lies close to the tectonic contact between the craton and the Neoproterozoic Araçuaí mobile melt. Blue sodalite-bearing syenites are found in almost all the igneous bodies of the SBAP as dykes or pegmatitic masses hosted by nepheline syenite. Economically viable quantities for the production of dimension stones are found only in the Floresta Azul alkaline complex, the Itaju do Colônia and Rio Pardo stocks and the Itarantim batholith.U-Pb ages obtained for titanite from Itaju do Colônia (732 ± 8 Ma) and Rio Pardo (714 ± 8) and Pb-Pb evaporation ages of zircon from Floresta Azul (696 ± 3 Ma) and Itarantim (722 ± 5 Ma). The geochronology of the SBAP shows that the anorogenic alkaline magmatism persisted for at least 58 Ma, demonstrating an extensional tectonic environment in the southern part of the São Francisco craton at this time. The data show that the rift phase which preceded the formation of the Araçuaí orogen was active until at least 700 Ma. The reported ages are similar to those found for the nepheline syenite host bodies, which supports the conclusions of the previous petrologic study demonstrating that blue sodalite is formed during the crystallization of these bodies. Two different processes are involved. In the magmatic process, sodalite occurs as disseminated and interstitial crystals among alkali feldspar crystals, and is associated with calcite and cancrinite formed by destabilization of nepheline. In the metasomatic process, discontinuous bands of sodalite are in sharp contact with nepheline syenite pegmatite, and its crystal aggregates often contain relict textures of nepheline and albite been replaced by sodalite.

  15. Geochemical characteristics of the Shujiadian Cu deposit related intrusion in Tongling: Petrogenesis and implications for the formation of porphyry Cu systems in the Middle-Lower Yangtze River Valley metallogenic belt, eastern China (United States)

    Wang, Shiwei; Zhou, Taofa; Yuan, Feng; Fan, Yu; Cooke, David R.; Zhang, Lejun; Fu, Bin; White, Noel C.


    Porphyry Cu deposits can form in intracontinental or post-collision settings; however, both the genesis of fertile magmas and the mechanism of metal enrichment remain controversial. The Shujiadian porphyry Cu deposit is located in the Tongling area of the Middle-Lower Yangtze River Valley metallogenic belt. It is hosted by the Shujiadian complex, which mainly consists of quartz diorite porphyry (143.7 ± 1.7 Ma) and pyroxene diorite (139.8 ± 1.6 Ma). They both belong to the calc-alkaline series, with enrichment in large-ion lithophile elements (LILE) and light rare earth elements (LREE), depletion in high field-strength elements (HFSE) and heavy rare earth elements (HREE), and slightly negative Eu anomalies. Both quartz diorite porphyry and pyroxene diorite have geochemical affinities with adakite, and their low MgO (1.5-3.7 wt%), and Ni (3.7-6.9 ppm), Cr (2.0-44 ppm), and Th/Ce contents (0.06-0.11) indicate that the intrusive rocks have some characteristics of adakite-like rocks derived from thickened lower crust and melts from metabasaltic rocks and eclogites. Plagioclases from the quartz diorite porphyry are andesine (An value = 31.8-40.5) and from the pyroxene diorite are felsic albite and oligoclase with large-scale zones and variable An value (An value = 8.9-18.3), Fe and Sr contents, which indicate that mixing of mafic and felsic magma may have occurred in the shallow magma chamber. Compared to the barren quartz diorite porphyry, relatively lower SiO2 contents (49.5-55.2 wt.%), higher εNd(t) values (- 7.4 to - 6.9), εHf(t) values (- 11.0 to - 9.1) compositions, Ti-in-zircon temperatures (714-785 °C), and variations of HREE contents of the mineralization-related pyroxene diorite suggest mixing with high-temperature mafic magma. Calculated Ce4 +/Ce3 + values of pyroxene diorite plot between the Ni-NiO buffer (NNO) and magnetite-hematite buffer (MH), and barren quartz diorite porphyry samples plot below the Ni-NiO buffer (NNO). Geochemical features of

  16. Northernmost Known Outcrop in North America of Lower Cretaceous Porphyritic Ocoite Facies (Ocoa, Chile) at Western Mexico: the Talpa Ocoite (United States)

    Zárate-del Valle, P. F.; Demant, A.


    At Talpa de Allende region in Western Mexico is located the northernmost known outcrop of ocoite facies (andesite): the Talpa ocoite (TO). The ocoite facies consists of an calk-alkaline andesitic rock rich in K and characterized by the presence of megacrysts of plagioclase (An48-65). TO belongs to the so-called Guerrero Terrane composed of plutono-volcanic and volcano-sedimentary sequences of the Alisitos-Teloloapan arc that was accreted to the North American craton at the end of the early Cretaceous (Lapierre et al., 1992, Can. J. Earth Sci. 29. 2478--2489). Geodynamically TO belongs to lithological sequence number IV or "Tecoman" of Tardy et al. (1994, Tectonophysics 230, 49--73). TO in hand-sample shows typical megacrysts (>1 cm) of plagioclase and clinopyroxene in a dark green aphanitic matrix. This andesitic lava has a shoshonitic character as evidenced by chemical composition: SiO_2 TiO_2 Al_2O_3 Fe_2O_3 MnO MgO CaO Na_2O K_2O P_2O_5 LOI % Ba Sr (ppm) 55.64 0.73 16.61 8.39 0.13 3.59 6.40 3.55 2.85 0.36 1.84% 1093 880 Under microscope TO is characterized by a porphyritic texture made of large labradorite phenocrysts (up to 3 cm) and clinopyroxene with a matrix made of plagioclase microlites; TO has been affected by a low grade metamorphism process belonging to the prehnite-pumpellite facies as it happens in Chile (Levi, 1969, Contr. Mineral. and Petrol. 24-1, p. 30--49). Electron microprobe analysis shows that plagioclase (An55-57) is partly transformed into albite (An7-9); clinopyroxene shows a variation in composition from Wo33En41Fs17 to Wo40En44Fs24 and it is transformed towards the margin first into amphibole and then into biotite. TO outcrops located at East of Talpa river are affected by a deep rubefaction process. TO is not characterized by the presence of bitumen as it occurs in Northern Chile (Nova-Muñoz et al., 2001, EUG XI Meeting, OS09 Supo09 PO, 606); TO is related in time with albian-cenomanian volcanogenic massive sulphides of Western Mexico

  17. Evolution of a very deeply subducted metasediment from As Sifah, northeastern coast of Oman (United States)

    Massonne, Hans-Joachim; Opitz, Joachim; Theye, Thomas; Nasir, Sobhi


    Near the coastal village of As Sifah, NE Oman, eclogite-facies rocks occur in the Saih Hatat window. We investigated a metapelite from this area, which is composed of mm-sized garnet and greenish phengite and minor epidote, blue amphibole, paragonite, albite, quartz, rutile, opaque phases, barite, and carbonate. Garnet exhibits a chemical zonation with Gro17Alm66Pyr6Spe11, Gro22Alm72.5Pyr5Spe0.5, and Gro25Alm65Pyr8Spe2 as inner core, mantle and outermost rim compositions. Inner portions of phengite have Si contents of up to 3.6 per formula unit (pfu), whereas rims are poorer in Si (3.2-3.4 pfu). We constructed a P-T pseudosection in the system Na2O-K2O-CaO-FeO-O2-MnO-MgO-Al2O3-SiO2-TiO2-H2O for the bulk-rock composition of the studied metapelite and contoured it by isopleths of various parameters such as the molar fractions of garnet components. Based on this contouring a P-T path was derived that starts at ultrahigh-pressure conditions. Garnet began to form at 25 kbar and 490 °C. Subsequently, temperatures increased and pressures decreased to finally reach P-T conditions of 13 kbar and 565 °C at which low-Si phengite, the outermost rim of garnet, Na-amphibole, epidote, quartz, magnetite, and rutile were in equilibrium. The P-T path is related to events in a subduction channel where the top of subducted oceanic crust, including the studied metasediments, was involved in an upwards-directed mass flow, resulting in the release of about 3 wt.% H2O by garnet formation from hydrous minerals such as chlorite and lawsonite. In order to get hints at the interaction of such hydrous fluids, we have analyzed the trace and minor elements in phengite. The contents of B, Rb, Cs, and Tl (20, 397, 6.7 and 1.7 ppm, respectively) are nearly constant over the entire Si range of potassic white mica. In contrast, the contents of Ba and Sr increase from 900 and 0.5 to 10500 and 14 ppm, respectively, with decreasing Si content in phengite. We hypothesize that this result reflects early

  18. Deep Water Compositions From the Los Angeles Basin and the Origin of Formation Water Salinity (United States)

    Boles, J.; Giles, G.; Lockman, D.


    elevated Ca/Na ratios and K/Na ratios which we attribute to dissolution and albitization of feldspar, mainly plagioclase, at the elevated burial temperatures. As is typical of most formation waters, Mg, Fe, and sulfate ions are highly depleted due to early formed pyrite, Fe-Mg siderite, and dolomite.

  19. Function and mechanism of assistant reducers in iron recovery by the direct reduction in tunnel kilns of hematite%赤铁矿石隧道窑直接还原助还原剂的作用及机理

    Institute of Scientific and Technical Information of China (English)

    何洋; 王化军; 孙体昌; 胡文韬; 李宏静


    Iron enrichment from refractory low-grade hematite was studied by using the method of direct reduction roasting in a tunnel kiln and magnetic separation. This study focused on the function and the mechanism of the assistant reducer NCP. Under the condi- tions of coal as the reducer with a mass fraction of 20% , CCO and NCP as the assistant reducers with mass fractions of 15% and 5% respectively, and roasting at 1 200 ℃for 8 h, a concentrate of the Fe grade of 92.61% with the Fe recovery of 92.38% can be pro- duced. The mechanisms of NCP were also investigated by X-ray diffraction and scanning electron microscopy. It is shown that NCP can react with quartz in the raw ore and generate natrosilite and albite, which can destroy the structure of the raw ore and induce a reaction between reducing gas and hematite to create Fe.%对隧道窑直接还原焙烧一磁选法处理低品位难选赤铁矿石进行了探讨,重点研究助还原剂NCP的作用及机理.以煤作还原剂,质量分数为20%,CCO和NCP为助还原剂,质量分数分别为15%和5%,在焙烧温度为1200℃,焙烧时间为8h的条件下,可以得到铁品位92.61%、铁回收率92.38%的铁精矿.利用X射线衍射和扫描电镜对助还原剂NCP的作用机理进行分析.结果表明NCP可以与原矿中石英发生反应,生成硅钠石和钠长石,破坏原矿结构,使还原性气体更易与赤铁矿接触发生还原反应生成金属铁.

  20. 40Ar/39Ar and K/Ar dating of low grade metamorphism: examples on metabasites from Central Chile (United States)

    Aguirre, L.; Feraud, G.; Fuentes, F.; Delbar, M.; Morata, D.


    Dating low to very low-grade burial metamorphic assemblages is often difficult because of (1) few mineral phases compositionally suitable to apply the 40Ar/39Ar and K-Ar methods, and (2) small amount in which these phases are commonly found. K-feldspar adularia, sericitic mica, and celadonite are the best known K-bearing secondary minerals. We present some successful attempts to analyse two distinct secondary phases from a same volcanic formation that allow to test the validity of the measured ages. These ages have been also compared with the crystallisation age of the volcanic rocks in which the secondary phases were lately developed. Adularia and sericite were selected from basic lava flows from a 3 to 13 km thick Cretaceous sequence from the Coastal Range of central Chile, at two different locations: the Bustamante Hill (west from Santiago), and the Cordón de Chacana, c. 80 km further north. Adularia came from a low-variance assemblage with pumpellyite, chlorite and low-albite contained in amygdules whereas sericite was present in milky-white strongly sericitized plagioclase crystals. While small clusters of rare fresh plagioclase grains from lava flows from Bustamante and Chacana displayed concordant plateau ages 119.4 ± 2.4 (2 sigma) and 118.7 ± 0.6 Ma, respectively, the adularia from the same formations gave sensibly younger ages around 94 Ma (high temperature steps), and 96.8 ± 0.2 Ma (plateau age) in Bustamante and Chacana, respectively. Sericite ages were measured in situ into single crystals of strongly transformed plagioclases. The relative proportion of sericite and plagioclase corresponding to each degasing step was monitored by measuring the Ca/K ratio (deduced from 37ArCa/39Ar_K). While intermediate ages were measured on some sericite of both sites (corresponding to a variable but permanent contribution of plagioclase on each step), a plateau age of 97.0 ± 1.6 Ma (concordant with adularia) could be obtained on a strongly sericitized plagioclase

  1. Monsoon variability for the past 4 ka derived from high-resolution analyses of sediments from lake Nam Co, central Tibetan Plateau (United States)

    Kasper, T.; Haberzettl, T.; Doberschütz, S.; Daut, G.; Mäusbacher, R.; Wang, J.; Zhu, L.; Wennrich, V.


    The presented project aims to reconstruct processes within lake Nam Co (central Tibetan Plateau; 4718 m a.s.l.), its environment and climatic conditions. By using a multi-proxy approach for this study we present high resolution data covering the past 4 ka. During a field campaign in September 2008 five gravity cores (68 cm to 115 cm length) were recovered in addition to one piston core with a total length of 11 m (water depth: 93 m). This study focuses on data from sediments of two gravity cores (NC08/01 Pilot 3 & Pilot 4). A wide spectrum of sedimentological, geochemical and mineralogical investigations was carried out. Results are presented for XRD measurements, XRF-core scans, grain size analysis and SEM-image analyses. Data are completed by an age-depth model using 210Pb and 137Cs analyses as well as eleven AMS 14C-ages. In addition this model is supported by excellent agreement between secular variations detected in one of the cores to geomagnetic field models. This is a significant improvement of the chronology as the catchments of most lacustrine systems on the plateau contain carbonates resulting in a carbon reservoir effect for radiocarbon dates. By the comparison of our record with the geomagnetic field models we assure that there is no change in this effect through time. Sediments exhibit homogeneous color and only minor variations regarding grain size distribution. According to the XRD measurements the main minerogenic components of the sediment, such as quartz, calcite, feldspars (albite & orthoclase) and muscovite show only minor fluctuations. In addition the presence of monohydrocalcite (CaCO3×H2O) (MHC), was proven by both XRD-measurements and SEM imaging. The presence of this metastable phase of CaCO3 is meant to be an indicator for intervals of cold climate or for evaporative settings (Li et al. 2008). Results of the high-resolution XRF-core scan (0.2 cm interval) show clear variability. After removing elements with too low counts 8 element scans

  2. Archaeological jade mystery solved using a 119-year-old rock collection specimen (United States)

    Harlow, G. E.; Davies, H. L.; Summerhayes, G. R.; Matisoo-Smith, E.


    In a recent publication (Harlow et al. 2012), a ~3200-year old small stone artefact from an archaeological excavation on Emirau Island, Bismarck Archipelago, Papua New Guinea was described and determined to be a piece of jadeite jade (jadeitite). True jadeitite from any part of New Guinea was not previously known, either in an archaeological or geological context, so this object was of considerable interest with respect to its geological source and what that would mean about trade between this source and Emirau Island. Fortuitously, the artefact, presumably a wood-carving gouge, is very unusual with respect to both pyroxene composition and minor mineral constituents. Pyroxene compositions lie essentially along the jadeite-aegirine join: Jd94Ae6 to Jd63Ae36, and without any coexisting omphacite. This contrasts with Jd-Di or Jd-Aug compositional trends commonly observed in jadeitites worldwide. Paragonite and albite occur in veins and cavities with minor titanite, epidote-allanite, and zircon, an assemblage seen in a few jadeitites. Surprisingly, some titanite contains up to 6 wt% Nb2O5 with only trace Ta and a single grain of a Y-Nb phase (interpreted as fergusonite) is present; these are unique for jadeitite. In a historical tribute to C.E.A. Wichmann, a German geologist who taught at Utrecht University, the Netherlands, a previously unpublished description of chlormelanite from the Torare River in extreme northeast Papua, Indonesia was given. The bulk composition essentially matches the pyroxene composition of the jade, so this sample was hypothesized as coming from the source. We were able to arrange a loan from the petrology collection at Utrecht University of the specimen acquired by Wichmann in 1893. In addition we borrowed stone axes from the Natural History Museum - Naturalis in Leiden obtained from natives near what is now Jayapura in eastern-most Papua. Petrography and microprobe analysis of sections of these samples clearly show that (1) Wichmann's 1893

  3. Genesis and formation conditions of deposits in the unique Strel'tsovka Molybdenum-Uranium ore field: New mineralogical, geochemical, and physicochemical evidence (United States)

    Aleshin, A. P.; Velichkin, V. I.; Krylova, T. L.


    The ambiguity of genetic interpretations of uranium ore formation at Mo-U deposits of the Strel’tsovka ore field led us to perform additional geochemical, mineralogical, and thermobarogeochemical studies. As a result, it has been established that closely related U and F were progressively gained in the Late Mesozoic volcanic rocks from the older basic volcanics (170 Ma) to the younger silicic igneous rocks (140 Ma). The Early Cretaceous postmagmatic hydrothermal epoch (140-125 Ma) is subdivided into preore, uranium ore, and first and second postore stages. The primary brannerite-pitchblende ore was formed in association with fluorite. At the first postore stage, this assemblage was replaced by a U-Si metagel, which was previously identified as coffinite. The metagel shows a wide compositional variation; its fine structure has been studied. The preore metasomatic alteration and related veined mineralization were formed under the effect of sodium (bicarbonate)-chloride solution at a temperature of 250-200°C. The uranium ore formation began with albitization and hematitization of rocks affected by supercritical fluid at 530-500°C; brannerite and pitchblende precipitated at 350-300°C. The chondrite-normalized REE patterns of pitchblende hosted in trachybasalt, trachydacite, and granite demonstrate a pronounced Sm-Nd discontinuity and a statistically significant tetrad effect of W type. These attributes were not established in REE patterns of rhyolites derived from the upper crustal magma chamber. This circumstance and a chronological gap of 5 Ma between silicic volcanism and ore formation do not allow us to suggest that uranium was derived from this magma chamber. According to the proposed model, the evolved silicic Li-F magma was a source of uranium. U4+, together with REE, was fractionated into the fluid phase as complex fluoride compounds. The uranium mineralization was deposited at a temperature barrier. It is suggested that hydromica alteration and the

  4. Eclogite-, amphibolite- and blueschist-facies rocks from Diego de Almagro Island (Patagonia): Episodic accretion and thermal evolution of the Chilean subduction interface during the Cretaceous (United States)

    Hyppolito, Thais; Angiboust, Samuel; Juliani, Caetano; Glodny, Johannes; Garcia-Casco, Antonio; Calderón, Mauricio; Chopin, Christian


    Few localities in the Patagonian Andes expose remnants of the Mesozoic Chilean paleo-accretionary complex. We focus on the Diego de Almagro Island high-pressure/low-temperature (HP/LT) Complex, a pluri-kilometer thick sequence comprising metavolcanic rocks with oceanic affinities and metasedimentary rocks. In this study, the deepest segments of the Chilean subduction interface in Patagonia are characterized for the first time. Despite its apparent homogeneity, the complex is actually composed of two tectonic units with distinct ages of metamorphism and thermal evolution: the garnet amphibolite (GA) and the underlying blueschist (BS) units. The GA unit mafic rocks exhibit epidote, phengite, titanite, rutile, chloritoid and paragonite inclusions in prograde garnet I, diopside + albite intergrows replacing omphacite inclusions in garnet II, and relict omphacite (XJd45) included in edenitic-pargasitic amphiboles. Thermobarometric results show that these rocks were buried along a relatively cold prograde path (c. 11 °C/km) and reached eclogite-facies near peak pressure conditions (c. 550-600 °C, 1.6 GPa). The GA unit underwent a pervasive stage of amphibolitization during decompression at c. 1.3 GPa. Field and petrological observations, together with multi-mineral Rb-Sr dating, indicate that amphibolitization of the GA unit took place along the subduction interface at c. 120 Ma in a slightly warmer subduction regime (c. 13-14 °C/km), in agreeement with the formation of coetanoeus amphibolites at c. 35 km. The underlying BS unit (i) yields four consistent Rb-Sr deformation ages of c. 80 Ma, i.e. 40 Ma younger than the overlying rocks from the GA unit; (ii) exhibits slightly cooler peak metamorphic conditions (c. 520-550 °C, 1.6 GPa) indicating burial along a prograde path of c. 10 °C/km (iii) does not show amphibolite-facies overprint as seen in the GA unit. After a long residence time under amphibolite-facies conditions, the amphibolitized rocks of the GA unit

  5. Mineralogical, IR-spectral and geochemical monitoring of hydrothermal alteration in a deformed and metamorphosed Jurassic VMS deposit at Arroyo Rojo, Tierra del Fuego, Argentina (United States)

    Biel, C.; Subías, I.; Acevedo, R. D.; Yusta, I.; Velasco, F.


    The Arroyo Rojo Zn-Pb-Cu volcanogenic massive sulfide deposit is the main deposit of the Fin del Mundo District in the Fuegian Andes, Argentina. This deposit is hosted by a Middle Jurassic volcanic and volcanoclastic sequence forming the Lemaire Formation. The latter consists, from the base up, of the following: rhyolitic and dacitic porphyritic rocks, ignimbrite, tuff, and flow. It is underlain by a pre-Jurassic basement and overlain by the hyaloclastic andesites of the Yahgán Formation. The Arroyo Rojo consists of stacked lenticular lenses that are associated with disseminated mineralization in both the footwall and the hanging wall. The internal structure of the ore lenses is marked by the occurrence of massive, semi-massive and banded facies, along with stringer and brecciated zones and minor ore disseminations. The mineral assemblage comprises mainly pyrite and sphalerite, with minor amounts of galena and chalcopyrite and rare pyrrhotite, arsenopyrite, tetrahedrite and bournonite. The ores and the volcanic host rocks have metamorphosed to greenschist facies and were overprinted by a penetrative tectonic foliation, which led to the development of mylonitic, and cataclastic textures, recrystallization and remobilization. Primary depositional characteristics and regional and hydrothermal alteration patterns were preserved despite deformation and metamorphism. Therefore, primary banding was preserved between facies boundaries. In addition, some remnants of magmatic origin are recognizable in preserved phenocrysts and volcaniclastic phenoclasts. Most of the volcanic and volcaniclastic rocks of the host sequence show a rhyolitic to rhyo-dacitic composition. Regional seafloor alteration, characterized by the presence of clinozoisite, Fe-chlorite and titanite, along with quartz and albite, is partially obliterated by hydrothermal alteration. The hydrothermal alteration is stratabound with the following assemblages, which developed from the base to top: (1) Quartz

  6. Theoretical Chemical Thermometry on Geothermal Waters: Problems and Methods (United States)

    Pang, Zhong-He; Reed, Mark


    Using a synthetic geothermal water, we examine the effect of errors in Al analyses on theoretical chemical geothermometry based on multicomponent chemical equilibrium calculations of mineral equilibria. A new approach named FixAl that entails the construction of a modified Q/K graph eliminates problems with water analyses lacking Al or with erroneous analyses of Al. This is made possible by forcing the water to be at equilibrium with a selected Al-bearing mineral, such as microcline. In a FixAl graph, a modified Q/K value is plotted against temperature for Al-bearing minerals. Saturation indices of nonaluminous minerals are plotted in the same way as in an ordinary Q/K graph. In addition to Al concentration errors, degassing of CO 2 and dilution of reservoir water interfere with computed equilibrium geothermometry. These effects can be distinguished in a Q/K graph by comparing curves for nonaluminous minerals to those of aluminous minerals then correcting for CO 2 loss and dilution by a trial and error method. Example geothermal waters from China, Iceland, and the USA that are used to demonstrate the methods show that errors in Al concentrations are common, and some are severe. The FixAl approach has proved useful for chemical geothermometry for geothermal waters lacking Al analysis and for waters with an incorrect Al analysis. The equilibrium temperatures estimated by the FixAl approach agree well with quartz, chalcedony, and isotopic geothermometers. The best choice of mineral for forced equilibrium depends on pH. For most neutral pH waters, microcline and albite work well; for more acidic waters, kaolinite or illite are good choices. Measured pH plays a critical role in computed equilibria, and we find that the best pH to use is the one to which the reported carbonate also applies. Commonly this is the laboratory pH instead of field pH, but the field pH is still necessary to constrain CO 2 degassing. Calculations on numerous waters in the 80-180°C reservoir

  7. Quality Aspects of a Marine Aggregate Deposit off the SE Euboea Island, Greece, for its Exploitation - Preliminary Results (United States)

    Anastasatou, Marianthi; Kapsimalis, Vasilios; Stamatakis, Michael; Tsoutsia, Antonia; Poulos, Serafeim; Rousakis, Grigoris; Karditsa, Aikaterini; Petrakis, Stelios; Aspiotis, Konstantinos; Papavlasopoulou, Nafsika; Stamatakis, Giorgos


    % according to a semi-quantitative estimation) with minor trace minerals, such as albite and clay minerals. On the basis of the qualitative characteristics, sediments on the inner continental shelf of SE Euboea can be classified as siliceous and being considered appropriate for potential exploitation, that is related also to its quantitatively characteristics. The relatively shallow depths (research program THALES-MARE (MIS: 375655) that is funded by the Operational Programme ''Education and lifelong learning, 2007-2013'' of the Ministry of Education and Religious Affairs, Culture and Sports.

  8. Geology of the Mid-Miocene Rooster Comb Caldera and Lake Owyhee Volcanic Field, eastern Oregon: Silicic volcanism associated with Grande Ronde flood basalt (United States)

    Benson, Thomas R.; Mahood, Gail A.


    The Lake Owyhee Volcanic Field (LOVF) of eastern Oregon consists of rhyolitic caldera centers and lava fields contemporaneous with and spatially related to Mid-Miocene Columbia River flood basalt volcanism. Previous studies delineated two calderas in the southeastern part of LOVF near Owyhee Reservoir, the result of eruptions of two ignimbrites, the Tuff of Leslie Gulch and the Tuff of Spring Creek. Our new interpretation is that these two map units are differentially altered parts of a single ignimbrite produced in a major phreatomagmatic eruption at ~ 15.8 Ma. Areas previously mapped as Tuff of Spring Creek are locations where the ignimbrite contains abundant clinoptilolite ± mordenite, which made it susceptible to erosion. The resistant intracaldera Tuff of Leslie Gulch has an alteration assemblage of albite ± quartz, indicative of low-temperature hydrothermal alteration. Our new mapping of caldera lake sediments and pre- and post-caldera rhyolitic lavas and intrusions that are chemically similar to intracaldera Tuff of Leslie Gulch point to a single ~ 20 × 25 km caldera, which we name the Rooster Comb Caldera. Erosion of the resurgently uplifted southern half of the caldera created dramatic exposures of intracaldera Tuff of Leslie Gulch cut by post-caldera rhyolite dikes and intrusions that are the deeper-level equivalents of lava domes and flows that erupted into the caldera lake preserved in exposures to the northeast. The Rooster Comb Caldera has features in common with more southerly Mid-Miocene calderas of the McDermitt Volcanic Field and High Rock Caldera Complex, including formation in a basinal setting shortly after flood basalt eruptions ceased in the region, and forming on eruption of peralkaline ignimbrite. The volcanism at Rooster Comb Caldera postdates the main activity at McDermitt and High Rock, but, like it, begins ~ 300 ky after flood basalt volcanism begins in the area, and while flood basalts don't erupt through the silicic focus, are

  9. REE Mineralization in Kiruna-type Magnetite-Apatite Ore Deposits: Magmatism and Metasomatism (United States)

    Harlov, D. E.


    ,K)Cl) fluids originating in the surrounding country rock or as fluids associated with metamorphic events such as regional albitization or actinolization. The abundance of (Y+REE)-bearing minerals in these deposits suggests that in addition to being mined for their Fe ore, they could also be economically mined for (Y+REE) as well.

  10. Petrology of HP/LT metapelitic rocks of an accretionary wedge, the Central Pontides, Turkey: evidence for tectonic stacking and syn-subduction exhumation (United States)

    Aygül, Mesut; Okay, Aral; Oberhänsli, Roland


    Cretaceous HP/LT chloritoid-bearing metapelitic rocks crop out widely in the central part of the Pontides, northern Turkey. They are associated with eclogite to blueschist-facies metabasites and represent deep levels of an underplated subduction-accretion complex, which is tectonically overlain by low-grade HP phyllite/metasandstone intercalation along an extensional shear zone. Close to the shear zone, the footwall micaschists consist of quartz, phengite, paragonite, chlorite, rutile with syn-kinematic albite porphyroblast formed by pervasive shearing during exhumation. This type of micaschists is tourmaline-bearing and their retrograde nature suggests high-fluid flux along shear zones. Peak metamorphic assemblages are partly preserved in the chloritoid-micaschist farther away from the shear zone. Three peak metamorphic assemblages are identified and their PT conditions are constrained by pseudosections produced by Theriak-Domino and by Raman spectra of carbonaceous material: 1) garnet-chloritoid-glaucophane with lawsonite pseudomorphs (P: 17.5 ± 1 Kbar, T: 390-450 °C) 2) chloritoid with glaucophane pseudomorphs (P: 16-18 Kbar, T: 475 ± 40 °C) and 3) relatively high-Mg chloritoid (17%) with jadeite pseudomorphs (22-25 Kbar; T: 440 ± 30 °C) in addition to phengite, paragonite, quartz, chlorite, rutile. The last mineral assemblage is interpreted as transformation of the chloritoid + glaucophane assemblage to chloritoid + jadeite paragenesis with increasing pressure. Absence of tourmaline suggests that the chloritoid-micaschist did not interact with B-rich fluids during zero strain exhumation. Peak metamorphic assemblages and PT estimates suggest tectonic stacking within wedge with different depths of burial. 40Ar/39Ar phengite age of a pervasively sheared footwall micaschist is constrained to 100.6 ± 1.3 Ma and that of a chloritoid-micaschist is constrained to 91.8 ± 1.8 Ma suggesting exhumation during on-going subduction. Coupling and exhumation of the

  11. Site investigation SFR. Boremap mapping of core drilled borehole KFR106

    Energy Technology Data Exchange (ETDEWEB)

    Winell, Sofia (Geosigma AB (Sweden))


    This report presents the result from the Boremap mapping of the core drilled borehole KFR106, drilled from an islet ca 220 m southeast of the pier above SFR. The borehole has a length of 300.13 m, and a bearing and inclination of 195.1 deg and -69.9 deg, respectively. The purpose of the location and orientation of the borehole is to investigate the possible occurrence of gently dipping, water-bearing structures in the area. The geological mapping is based on simultaneous study of drill core and borehole image (BIPS). The two lowermost meters of the drill core was mapped in Boremap without access to complementary BIPS-image. The dominating rock type, which occupies 72% of KFR106, is fine- to medium-grained, metagranite granodiorite (rock code 101057), which is foliated with a medium to strong intensity. Pegmatite to pegmatitic granite (rock code 101061) is the second most common rock type and it occupies 16% of the mapped interval. It is also frequent as smaller rock occurrences (< 1 m) in other rock types throughout the borehole. Subordinate rock types are fine- to medium-grained granite (rock code 111058), felsic to intermediate meta volcanic rock (rock code 103076), fine- to medium-grained metagranitoid (rock code 101051) and amphibolite (rock code 102017). Totally 49% of the rock in KFR106 has been mapped as altered, where muscovitization and oxidation is the two most common. Additional shorter intervals of alterations are in decreasing order of abundance quartz dissolution, epidotization, argillization, albitization, chloritization, laumontization and carbonatization. A total number of 2801 fractures are registered in KFR106. Of these are 1059 open, 1742 sealed and 84 partly open. This result in the following fracture frequencies: 6.0 sealed fractures/m, 3.7 open fractures/m and 0.3 partly open fractures/m. In addition there are 5 narrow brecciated zones, and 20 sealed networks with a total length of 18 m. The most frequent fracture fillings in KFR106 are

  12. Relative contributions of crust and mantle to the origin of the Bijli Rhyolite in a palaeoproterozoic bimodal volcanic sequence (Dongargarh Group), central India

    Indian Academy of Sciences (India)

    Sarajit Sensarma; S Hoernes; Dhruba Mukhopadhyay


    New mineralogical, bulk chemical and oxygen isotope data on the Palaeoproterozoic Bijli Rhyolite, the basal unit of a bimodal volcanic sequence (Dongargarh Group) in central India, and one of the most voluminous silicic volcanic expressions in the Indian Shield, are presented. The Bijli Rhyolite can be recognized as a poorly sorted pyroclastic deposit, and comprises of phenocrystic K-feldspar + albite ± anorthoclase set in fine-grained micro-fragmental matrix of quartz-feldsparsericite- chlorite-iron-oxide ± calcite. The rocks are largely metaluminous with high SiO2, Na2O+ KO, Fe/Mg, Ga/Al, Zr, Ta, Sn, Y, REE and low CaO, Ba, Sr contents; the composition points to an ‘A-type granite’ melt. The rocks show negative Cs-, Sr-, Eu- and Ti- anomalies with incompatible element concentrations 2–3 times more than the upper continental crust (UCC). LREE is high (La/Yb ∼20) and HREE 20-30 times chondritic. 18 Owhole-rock varies between 4.4 and 7.8‰(mean 5.87 ± 1.26‰). The Bijli melt is neither formed by fractionation of a basaltic magma, nor does it represent a fractionated crustal melt. It is shown that the mantle-derived high temperature basaltic komatiitic melts/high Mg basalts triggered crustal melting, and interacted predominantly with deep crust compositionally similar to the Average Archaean Granulite (AAG), and a shallower crustal component with low CaO and Al2O3 to give rise to the hybrid Bijli melts. Geochemical mass balance suggests that ∼30% partial melting of AAG under anhydrous condition, instead of the upper continental crust (UCC) including the Amgaon granitoid gneiss reported from the area, better matches the trace element concentrations in the rocks. The similar Ta/Th of the rhyolites (0.060) and average granulite (0.065) vs. UCC (0.13) also support a deep crustal protolith. Variable contributions of crust and mantle, and action of hydrothermal fluid are attributed for the spread in 18Owhole-rock values. The fast eruption of high

  13. Mineralogy and geochemistry of granitoids from Kinnaur region, Himachal Higher Himalaya, India: Implication on the nature of felsic magmatism in the collision tectonics

    Indian Academy of Sciences (India)

    Brajesh Singh; Santosh Kumar; Masao Ban; Kazuo Nakashima


    Felsic magmatism in the southern part of Himachal Higher Himalaya is constituted by Neoproterozoic granite gneiss (GGn), Early Palaeozoic granitoids (EPG) and Tertiary tourmaline-bearing leucogranite (TLg). Magnetic susceptibility values ($\\lt$3 ×10$^{−3}$ SI), molar Al$_2$O$^3$/(CaO+Na$_2$O+K$_2$O) ($\\geq$1.1), mineral assemblage (bt–ms–pl–kf–qtz ± tur ± ap), and the presence of normative corundum relate these granitoids to peraluminous S-type, ilmenite series (reduced type) granites formed in a syncollisional tectonic setting. Plagioclase from GGn (An$_{10}$–An$_{31}$) and EPG (An$_{15}$–An$_{33}$) represents oligoclase to andesine and TLg (An$_2$–An$_{15}$) represents albite to oligoclase, whereas compositional ranges of K-feldspar are more or less similar (Or$_{88}$ to Or$_{95}$ in GGn, Or$_{86}$ to Or$_{97}$ in EPG and Or$_{87}$ to Or$_{94}$ in TLg). Biotites in GGn (Mg/Mg+Fe$^t$ = 0.34–0.45), EPG (Mg/Mg+Fe$^t$ = 0.27–0.47), and TLg (Mg/Mg+Fe$^t$ = 0.25–0.30) are ferribiotites enriched in siderophyllite, which stabilised between FMQ and HM buffers and are characterised by dominant 3Fe$\\rightleftarrows$2Al, 3Mg$\\rightleftarrows$2Al substitutions typical of peraluminous (S-type), reducing felsic melts. Muscovite in GGn (Mg/Mg+Fe$^t$ = 0.58–0.66), EPG (Mg/Mg+Fe$^t$ = 0.31−0.59), and TLg (Mg/Mg+Fet = 0.29–0.42) represent celadonite and paragonite solid solutions, and the tourmaline fromEPG and TLg belongs to the schorl-elbaite series, which are characteristics of peraluminous, Li-poor, biotite-tourmaline granites. Geochemical features reveal that the GGn and EPG precursor melts were most likely derived from melting of biotite-rich metapelite and metagraywacke sources, whereas TLg melt appears to have formed from biotite-muscovite rich metapelite and metagraywacke sources. Major and trace elements modelling suggest that the GGn, EPG and TLg parental melts have experienced low degrees (∼13, ∼17 and ∼13%, respectively) of kf

  14. Dawsonite cement in the Triassic Lam Formation, Shabwa Basin, Yemen: A natural analogue for a potential mineral product of subsurface CO{sub 2} storage for greenhouse gas reduction

    Energy Technology Data Exchange (ETDEWEB)

    Worden, Richard H. [Department of Earth and Ocean Sciences, University of Liverpool, Brownlow Street, Liverpool L69 3GP (United Kingdom)


    carbon dioxide from a moderately negative source, possibly of magmatic or basement origins. Dawsonite may thus be the result of a mass influx of deep (e.g. magmatic) carbon dioxide that pushed the Lam Formation into the dawsonite stability field at the expense of albite. [Author].

  15. Evolution of fluid-rock interaction in the Reykjanes geothermal system, Iceland: Evidence from Iceland Deep Drilling Project core RN-17B (United States)

    Fowler, Andrew P. G.; Zierenberg, Robert A.; Schiffman, Peter; Marks, Naomi; Friðleifsson, Guðmundur Ómar


    We describe the lithology and present spatially resolved geochemical analyses of samples from the hydrothermally altered Iceland Deep Drilling Project (IDDP) drill core RN-17B. The 9.3 m long RN-17B core was collected from the seawater-dominated Reykjanes geothermal system, located on the Reykjanes Peninsula, Iceland. The nature of fluids and the location of the Reykjanes geothermal system make it a useful analog for seafloor hydrothermal processes, although there are important differences. The recovery of drill core from the Reykjanes geothermal system, as opposed to drill cuttings, has provided the opportunity to investigate evolving geothermal conditions by utilizing in-situ geochemical techniques in the context of observed paragenetic and spatial relationships of alteration minerals. The RN-17B core was returned from a vertical depth of ~ 2560 m and an in-situ temperature of ~ 345 °C. The primary lithologies are basaltic in composition and include hyaloclastite breccia, fine-grained volcanic sandstone, lithic breccia, and crystalline basalt. Primary igneous phases have been entirely pseudomorphed by calcic plagioclase + magnesium hornblende + chlorite + titanite + albitized plagioclase + vein epidote and sulfides. Despite the extensive hydrothermal metasomatism, original textures including hyaloclastite glass shards, lithic clasts, chilled margins, and shell-fragment molds are superbly preserved. Multi-collector LA-ICP-MS strontium isotope ratio (87Sr/86Sr) measurements of vein epidote from the core are consistent with seawater as the dominant recharge fluid. Epidote-hosted fluid inclusion homogenization temperature and freezing point depression measurements suggest that the RN-17B core records cooling through the two-phase boundary for seawater over time to current in-situ measured temperatures. Electron microprobe analyses of hydrothermal hornblende and hydrothermal plagioclase confirm that while alteration is of amphibolite-grade, it is in disequilibrium

  16. The Iceland Deep Drilling Project: (III) Evidence for amphibolite grade contact metamorphism in an active geothermal system (United States)

    Marks, N.; Schiffman, P.; Zierenberg, R. A.; Franzson, H.


    One of the scientific goals of the Iceland Deep Drilling Project is to reach the depths of transition from greenschist to amphibolite grade metamorphism in an active geothermal system. The deepest borehole to date in the Reykjanes system is RN-17, which was drilled to a depth of 3082 m. This well had been considered as a candidate for deepening by the IDDP until it collapsed during a flow test in November 2005. Temperatures in the lower portion of the borehole were never recorded due to an obstruction at 2100 m depth, but are estimated to be approximately 340°C. Epidote, albite, and actinolite are ubiquitous within pillow basalt, hyaloclastite, and in veins, implying that greenschist grade conditions have been attained throughout much of the well below approximately 1200 m. Intrusive lithologies constitute approximately 50% of the observed cuttings between 2600 and 2700 m. These intrusive rocks have produced small, but recognizable contact metamorphic effects characterized by granoblastic hornfels consisting of amphibolite grade assemblages of quartz + anorthite + diopside + magnetite + titanite. These have, in turn, been locally cut by actinolite veins, presumably reflective of the present-day, thermal state of the hydrothermal system at these depths. Based on their siliceous bulk composition, we believe the hornfels represent the thermally- recrystallized products of earlier-formed, hydrothermal veins consisting of quartz, epidote, and actinolite. The metamorphic plagioclase is distinctly more anorthitic (An90 to An98) than igneous plagioclase in adjacent mafic intrusives (An33 to An80) and also exhibits consistently lower Mg content and higher iron (up to 2.07 wt.% as Fe2O3). Stoichiometry implies that much of the iron in hydrothermal anorthite is Fe3+, which may imply recrystallization from precursor epidote under relatively oxidizing conditions. Diopside compositions (average Wo0.48En0.27Fs0.25) are consistently less calcic than hydrothermal clinopyroxenes

  17. Hydrothermal alteration in the Reykjanes geothermal system: Insights from Iceland deep drilling program well RN-17 (United States)

    Marks, Naomi; Schiffman, Peter; Zierenberg, Robert A.; Franzson, Hjalti; Fridleifsson, Gudmundur Ó.


    plagioclase, grandite garnet, prehnite, epidote, hydrothermal clinopyroxene, and titanite. In contrast, crystalline basalts and intrusive rocks display a range in alteration intensity from essentially unaltered to pervasive and nearly complete albitization of igneous feldspar and uralitization of clinopyroxene. Hydrothermal anorthite (An92-An98) occurs in veins in the most altered basalt cuttings and is significantly more calcic than igneous feldspar (An48-An79). Amphibole compositions change from actinolite to hornblende at depth. Hydrothermal clinopyroxene, which occurs in veins, has greater variation in Fe content and is systematically more calcic than igneous pyroxene and also lacks uralitic textures. Solid solutions of prehnite, epidote, and garnet indicate evolving equilibria with respect to aluminum and ferric iron.

  18. Mineral composition control on inter-mineral iron isotopic fractionation in granitoids (United States)

    Wu, Hongjie; He, Yongsheng; Bao, Leier; Zhu, Chuanwei; Li, Shuguang


    This study reports elemental and iron isotopic compositions of feldspar and its coexisting minerals from four Dabie I-type granitoids to evaluate the factors that control inter-mineral Fe isotopic fractionation in granitoids. The order of heavy iron isotope enrichment is feldspar > pyrite > magnetite > biotite ≈ hornblende. Feldspar has heavier iron isotopic compositions than its co-existing magnetite (Δ56Feplagioclase-magnetite = +0.376‰ to +1.084‰, Δ56Fealkali-feldspar-magnetite = +0.516‰ to +0.846‰), which can be attributed to its high Fe3+/Fetot ratio and low coordination number (tetrahedrally-coordinated) of Fe3+. Δ56Femagnetite-biotite of coexisting magnetite and biotite ranges from 0.090‰ to 0.246‰. Based on homogeneous major and iron isotopic compositions of mineral replicates, the inter-mineral fractionation in this study should reflect equilibrium fractionation. The large variations of inter-mineral fractionation among feldspar, magnetite and biotite cannot be simply explained by temperature variation, but strongly depend on mineral compositions. The Δ56Feplagioclase-magnetite and Δ56Fealkali-feldspar-magnetite are positively correlated with albite mode in plagioclase and orthoclase mode in alkali-feldspar, respectively. This could be explained by different Fe-O bond strength in feldspar due to different Fe3+/∑Fe or different crystal parameters. The Δ56Femagnetite-biotite increases with decreasing Fe3+/∑Febiotite and increasing mole (Na + K)/Mgbiotite, indicating a decrease of β factor in low Fe3+/∑Fe and high (Na + K)/Mg biotite. High-silica leucosomes from Dabie migmatites with a feldspar accumulation petrogenesis have higher δ56Fe values (δ56Fe = 0.42-0.567‰) than leucosome that represents pristine partial melt (δ56Fe = 0.117 ± 0.016‰), indicating that accumulation of feldspar could account for high δ56Fe values of these rocks. High δ56Fe values are also predicted for other igneous rocks that are mainly composed of

  19. Tectono-metallogenetic evolution of the Fe-Cu deposit of Dominga, northern Chile (United States)

    Veloso, E.; Cembrano, J.; Arancibia, G.; Heuser, G.; Neira, S.; Siña, A.; Garrido, I.; Vermeesch, P.; Selby, D.


    The Dominga district in northern Chile (2082 Mt at 23.3 % Fe, 0.07 % Cu) shows a spatial and genetic affinity among distinctive structural elements and Fe-Cu-rich paragenetic mineral assemblages. Deep seated, NE-to-E striking structural elements form a right-lateral duplex-like structural system (early structural system, ESS) that cuts a regionally extensive alteration (stage I) zone. The EES system served as a locus and as path for the emplacement of biotite-magnetite alteration/mineralization (stage IIa) as veins and Fe-bearing layers following altered volcano sedimentary strata. NW-striking actinolite-magnetite hydrothermal breccias, coeval with and part of the ESS, include apatite (stage IIb) crystallized at 127 ± 15 Ma (U-Pb, 2σ). The ESS was also the locus of subsequent alteration/mineralization represented by K-feldspar, epidote, and albite (stage IIIa) and Fe-Cu-rich (vermiculite-anhydrite-chalcopyrite, stage IIIb) mineral associations. Shallowly developed, NNE-striking, left-lateral structural elements defining the El Tofo Structural System (ETSS)—probably part of the Atacama Fault System—clearly crosscut the ESS. Minerals associated with alteration/mineralization stage IIIb also occur as veins and as part of hydrothermal breccias of the ETSS, marking the transition from the ESS to ETSS. Molybdenite associated with alteration/mineralization stage IIIb yielded a Re-Os age of 127.1 ± 0.7 Ma (2σ). Both the ESS and ETSS were cut by left-lateral, NW- to E-striking shallowly developed structural elements (Intermediate Structural System, ISS) on which a hematite-calcite assemblage (stage IV) occurs mostly as infill material of veins and fault veins. The ISS is cut by N-striking, left-lateral, and shallowly developed structural elements (Late Structural System, LSS) showing no evidence of alteration/mineralization. Estimated strain and stress fields indicate an overall NW-trending shortening/compression and NE-trending stretching/tension strike-slip regime

  20. Brittle tectonothermal evolution in the Forsmark area, central Fennoscandian Shield, recorded by paragenesis, orientation and 40Ar/ 39Ar geochronology of fracture minerals (United States)

    Sandström, Björn; Tullborg, Eva-Lena; Larson, Sven Åke; Page, Laurence


    In this paper, we show how studies of fracture mineral paragenesis, their orientation and 40Ar/ 39Ar geochronology can be applied in order to recognise the brittle tectonothermal evolution in an area. Samples were selected from nearly 18 km of drill cores from the upper 1 km of the Fennoscandian Shield obtained during the site investigation for a repository of spent nuclear fuel in Forsmark, central Sweden. Four major events of fracturing and/or reactivation of fractures associated with fracture mineralisation have been distinguished. The first event was characterised by precipitation of epidote, quartz and chlorite, along preferably sub-horizontal and gently-dipping fractures or steep, WNW-ESE to NW-SE fractures. Precipitation occurred between 1.8 and 1.1 Ga, possibly during the late stage of the Svecokarelian orogeny close to 1.8-1.7 Ga. The second event is associated with precipitation of hematite-stained adularia and albite, prehnite, laumontite, calcite and chlorite, preferably along steep, ENE-WSW to NNE-SSW and NNW-SSE fractures. Precipitation occurred around 1107 ± 7 to 1034 ± 3 Ma, probably due to effects from the Sveconorwegian orogeny. This event was followed by a period with dissolution of fracture minerals and subsequent precipitation of mainly calcite, quartz, pyrite and asphaltite during the Palaeozoic. The formation fluid emanated from an overlying organic-rich sedimentary cover. Precipitation occurred during reactivation of Proterozoic fractures, but formation of new fractures is also inferred, possibly due to far-field effects of the Caledonian orogeny, or elevated hydrostatic pressure due to its foreland basin. The latest event is dominated by clay minerals, chlorite and calcite along hydraulically conductive fractures. These minerals are prominent along sub-horizontal and gently-dipping fractures, but also occur in sets of steeply-dipping fractures. It is inferred that the hydraulically conductive fractures are Proterozoic structures in which

  1. Solid oxide electrolyser cell

    Energy Technology Data Exchange (ETDEWEB)

    Hoejgaard Jensen, S.


    Solid oxide fuel cells (SOFCs) produced at Riso National Laboratory was tested as steam electrolysers under various current densities, operating temperatures and steam partial pressures. At 950 deg. C and a cell voltage of 1.48V the current density was -3.6 A/cm{sup 2} with app. 30% H{sub 2} + 70% H{sub 2}O in the inlet gas and a H{sub 2}O utilization of app. 40%. The tested SOECs were also used for CO{sub 2} electrolysis. Economy studies of CO and H2 production show that especially H{sub 2} production can be competitive in areas with cheap electricity. Assuming the above described initial performance and a lifetime of 10 years it is possible to achieve a production price of 0.7 US dollar/kg H{sub 2} with an electricity price of 1.3 US cent/kWh. The cell voltage was measured as function of time. In test of about two month of duration a long-term degradation was observed. At 850 deg. C, -0.5 A/cm{sup 2} with 50 vol% H{sub 2} the degradation rate was app. 20 mV/1000h. It was shown that the degradation happens at Ni/YSZ-electrode. The long term degradation is probably caused by coarsening of the Ni-particles. After onset of electrolysis operation a transient passivation/reactivation phenomena with duration of several days was observed. It was shown that the phenomenon is attributed to the SiO{sub 2} contamination at the Ni/YSZ electrode-electrolyte interface. The SiO{sub 2} arises from the albite glass sealing (NaAlSi{sub 3}O{sub 8}) that surrounds the electrode. Si may enter the Ni/YSZ electrode via the reaction Si(OH){sub 4}(g) {r_reversible} SiO{sub 2}(l)+H{sub 2}O(g). At the active sites of the Ni/YSZ electrode steam is reduced via the reaction H{sub 2}O - 2e {yields} H{sub 2}+O{sup 2-} . This shifts the equilibrium of the first reaction to form SiO{sub 2}(l) at the active sites. After a certain time the sealing crystallizes and the SiO{sub 2}(l) evaporates from the active sites and the cell reactivates. The passivation is shown to relate to a build up of a

  2. Turbidity anomaly and probability of slope failure following the 2011 Great Tohoku Earthquake (United States)

    Noguchi, T.; Tanikawa, W.; Hirose, T.; Lin, W.; Kawagucci, S.; Yoshida, Y.; Honda, M. C.; Takai, K.; Kitazato, H.; Okamura, K.


    Turbidity anomaly at seafloor is often observed immediately after earthquakes (Thunnell et al., 1999: Mikada et al., 2006). Such turbidity anomaly at deepsea is thought to be results of the seismically induced landslides at trench slopes. Turbidity distribution was observed using turbidity meter (Seapoint Sensors Inc.) at the mainshock area of the 2011 off the Pacific coast Tohoku earthquake (Mw 9.0) one month after the event. Turbidity anomalies, in which the turbidity increased with depth, were observed near the seafloor at all four sites. The thickness of the anomalous zones increased with water depth; the thickness at station B, the deepest measurement site, was about 1300 m above the seafloor and the average particle concentration which is equivalent to turbidity in the zone was 1.5 mg/L. We analyzed the mineral composition and grain size distribution of the suspended particle collected one month after the earthquake and shallow sediment core collected before the earthquake at the mainshock area. The grain size of the suspended particles was ranged from 1 to 300μm, and XRD analysis confirmed the presence of chlorite, illite, quartz, and albite in the particles. These characteristics are similar to the subsurface sediment material. Earlier studies (Prior, 1984) have introduced a mathematical model for analysis of submarine slope stability that include the effect of vertical and horizontal seismic accelerations caused by the earthquake. We analyzed slope instability on the basis of their model using the physical properties (density and shear strength) of the shallow sediment core materials and the acceleration of 2011 off the Pacific coast Tohoku earthquake. Our results show that a submarine landslide can be induced by a very large ground acceleration, as high as 3 m/s2, even if the sediment layer on the sliding surface is not very thick. We interpret the high turbidity observed one month after the Tohoku earthquake as the result of thin submarine landsliding

  3. Cl-rich hydrous mafic mineral assemblages in the Highiș massif, Apuseni Mountains, Romania (United States)

    Bonin, Bernard; Tatu, Mihai


    The Guadalupian (Mid-Permian) Highiș massif (Apuseni Mountains, Romania) displays a bimodal igneous suite of mafic (gabbro, diorite) and A-type felsic (alkali feldspar granite, albite granite, and hybrid granodiorite) rocks. Amphibole is widespread throughout the suite, and yields markedly high chlorine contents. Three groups are identified: Cl-rich potassic hastingsite (2.60-3.40 wt% Cl) within A-type felsic rocks and diorite, mildly Cl-rich pargasite to hornblende (0.80-1.90 wt% Cl) within gabbro, and low F-Cl hornblende within gabbro and hybrid granodiorite. Coexisting biotite is either Cl-rich within diorite, or F-Cl-poor to F-rich within A-type felsic rocks. Chlorine and fluorine are distributed in both mafic phases, according to the F-Fe and Cl-Mg avoidance rules. The low-Ti contents suggest subsolidus compositions. Cl-rich amphibole within diorite and A-type felsic rocks yields a restricted temperature range - from 575 °C down to 400 °C, whereas mildly Cl-rich amphibole within gabbro displays the highest range - from 675 to 360 °C. Temperatures recorded by Cl-rich biotite within diorite range from 590 to 410 °C. Biotite within A-type felsic rocks yields higher temperatures than amphibole: the highest values- from 640 to 540 °C - are recorded in low-F-Cl varieties, whereas the lowest values- from 535 to 500 °C - are displayed by F-rich varieties. All data point to halogen-rich hydrothermal fluids at upper greenschist facies conditions percolating through fractures and shear zones and pervasively permeating the whole Highiș massif, with F precipitating as interstitial fluorite and Cl incorporating into amphibole, during one, or possibly several, hydrothermal episodes that would have occurred during a ~ 150 My-long period of time extending from the Guadalupian (Mid-Permian) to the Albian (Mid-Cretaceous).

  4. Origin and evolution of ore-forming fluids in the Hemushan magnetite-apatite deposit, Anhui Province, Eastern China, and their metallogenic significance (United States)

    Luo, Gan; Zhang, Zhiyu; Du, Yangsong; Pang, Zhenshan; Zhang, Yanwen; Jiang, Yongwei


    The Middle-Lower Yangtze River Metallogenic Belt in the northern Yangtze Block is one of the most important economic mineral districts in China. The Hemushan deposit is a medium-class Fe deposit located in the southern part of the Ningwu iron ore district of the Middle-Lower Yangtze River Metallogenic Belt. The Fe-orebodies are mainly hosted in the contact zone between diorite and Triassic marble. The actinolite-phlogopite-apatite-magnetite ore shows metasomatic/filling textures and disseminated/mesh-vein structures. Based on evidences and petrographic observations, the ore-forming process can be divided into three distinct periods-the early metallogenic period (albite-diopside stage), the middle metallogenic period (magnetite stage and hematite stage), and the late metallogenic period (quartz-pyrite stage and carbonate stage). Fluid inclusion studies show four types of inclusions: type I daughter mineral-bearing three-phase inclusions (L + V + S), type II vapor-rich two-phase inclusions (L + V), type III liquid-rich two phase inclusions (L + V), and minor type IV liquid-phase inclusions (L). Apatites from the magnetite stage contain type I, type II and type III inclusions; anhydrites from the hematite stage mainly contain abundant type II inclusions and relatively less type I inclusions; quartz and calcite from the late metallogenic stage are mainly characterized by type III inclusions. Laser Raman spectroscopy and microthermometry of fluid inclusions show that the ore-forming fluids broadly correspond to unsaturated NaCl-H2O system. From the magnetite stage to the carbonate stage, the ore-forming fluids evolved from moderate-high temperature (average 414 °C), moderate salinity (average 25.01 wt.% NaCl equiv.) conditions to low temperature (average 168 °C), low salinity (average 6.18 wt.% NaCl equiv.) conditions. Hydrogen and oxygen isotopic studies indicate that the ore-forming fluid during the early stage of middle metallogenic period was mainly of magmatic

  5. Protolith age of Santa Maria Chico granulites dated on zircons from an associated amphibolite-facies granodiorite in southernmost Brazil

    Directory of Open Access Journals (Sweden)

    Léo A. Hartmann


    Full Text Available U-Pb dating of zircon was undertaken with the Beijing SHRIMP II (sensitive high resolution ion microprobe on anamphibolite facies granodiorite and an almandine-albite granulite from the Santa Maria Chico Granulitic Complex, southern Brazilian Shield. This work was also done to unravel protolith ages which are often hidden in the array of partly reset data. The obtained metamorphic ages of the granodiorite gneiss and the granulite are 2035 ± 9 Ma and 2006 ± 3 Ma, respectively. These data are within the range of metamorphic ages determined in previous studies (2022 ± 18 Ma and 2031 ± 40 Ma. However, protolith ages for the granodiorite (2366 ± 8 Ma and the granulite (2489 ± 6 Ma were obtained which are outside the previously recognized range (> 2510-2555 Ma. The magmatic protolith age of the granodiorite refers to a previously little known magmatic event in the shield. Further investigations may demonstrate that amphibolite facies zircon crystals are useful as a window into geological events in associated granulites, because zircon ages are blurred in the studied granulites.Um granodiorito de fácies anfibolito e um almandina-albita granulito do Complexo Granulítico Santa Maria Chico, porção sul do Escudo Brasileiro, foram datados pelo método U-Pb em zircão por Beijing SHRIMP II (sensitive high resolution ion microprobe. Esta investigação inclui a determinação das idades de protólitos que estão ocultas no conjunto de dados parcialmente re-equilibrados. As idades metamórficas obtidas no gnaisse granodiorítico e no granulito são 2035 ±9 Ma e 2006 ±3 Ma, respectivamente. Esses dados estão dentro da variação das idades metamórficas determinadas em estudos anteriores (2022 ±18 Ma e 2031 ±40 Ma. No entanto, as idades do protólito do granodiorito (2366 ±8 Ma e do granulito (2489 ±6 Ma estão fora da variação de idades ( > 2510-2555 Ma reconhecidas anteriormente. A idade magmática do protólito do granodiorito corresponde

  6. Pore Scale Heterogeneity in the Mineral Distribution and Surface Area of Porous Rocks (United States)

    Lai, Peter; Krevor, Sam


    An important control on rate of interfacial processes between minerals and aqueous solutions such as nucleation of solids, and mineral dissolution and growth is reactive surface area. In geochemical modelling, the continuum hypothesis is based on the assumption that the system can be represented by a sufficiently large number of representative elemental volumes. There has been recent interest in studying the impact of this assumption on reaction-transport coupled systems. In this study, the impact of pore-scale heterogeneity on the distribution of reactive surface area is discussed. 3D images obtained using x-ray micro-tomography were used to characterise the distribution of reactive surface area. The results were compared to independent observations. Mineral identification using x- ray diffraction and fluorescence suggested general agreement with CT analysis. Nitrogen BET surface areas were one to two orders of magnitude higher than measurements from x-ray imagery. Co- registered images of Berea sandstone from x-ray and energy dispersive spectroscopy imagery suggested that quartz, K-feldspar and most clays could be identified. However, minor minerals such as albite and illite did not exhibit enough contrast. In Berea sandstone, mineral surface area fraction was poorly correlated to the mineral volumetric fraction. Clay and feldspar minerals exhibited higher surface area fractions than bulk mineralogy suggested. In contrast, in the Edwards carbonate samples, modal mineral composition correlated with mineral-specific surface area. Berea sandstone revealed a characteristic pore size at which a surface area distribution may be used to quantify heterogeneity. Conversely, the carbonate samples suggested a continuous range of pore sizes across length scales. A comparison with pore network model simulations from the literature was made. First order estimates of mineral specific correlations between geometric area measured in the x-ray images were used to convert the CT

  7. Role of evaporitic sulfates in iron skarn mineralization: a fluid inclusion and sulfur isotope study from the Xishimen deposit, Handan-Xingtai district, North China Craton (United States)

    Wen, Guang; Bi, Shi-Jian; Li, Jian-Wei


    The Xishimen iron skarn deposit in the Handan-Xingtai district, North China Craton, contains 256 Mt @ 43 % Fe (up to 65 %). The mineralization is dominated by massive magnetite ore along the contact zone between the early Cretaceous Xishimen diorite stock and middle Ordovician dolomite and dolomitic limestones with numerous intercalations of evaporitic beds. Minor lenticular magnetite-dominated bodies also occur in the carbonate rocks proximal to the diorite stock. Hydrothermal alteration is characterized by extensive albitization within the diorite stock and extreme development of magnesian skarn along the contact zone consisting of diopside, forsterite, serpentine, tremolite, phlogopite, and talc. Magmatic quartz and amphibole from the diorite and hydrothermal diopside from the skarns contain abundant primary or pseudosecondary fluid inclusions, most of which have multiple daughter minerals dominated by halite, sylvite, and opaque phases. Scanning electron microscopy (SEM) and laser Raman spectrometry confirm that pyrrhotite is the predominant opaque phase in most fluid inclusions, in both the magmatic and skarn minerals. These fluid inclusions have total homogenization temperatures of 416-620 °C and calculated salinities of 42.4-74.5 wt% NaCl equiv. The fluid inclusion data thus document a high-temperature, high-salinity, ferrous iron-rich, reducing fluid exsolved from a cooling magma likely represented by the Xishimen diorite stock. Pyrite from the iron ore has δ34S values ranging from 14.0 to 18.6 ‰, which are significantly higher than typical magmatic values (δ34S = 0 ± 5 ‰). The sulfur isotope data thus indicate an external source for the sulfur, most likely from the evaporitic beds in the Ordovician carbonate sequences that have δ34S values of 24 to 29 ‰. We suggest that sulfates from the evaporitic beds have played a critically important role by oxidizing ferrous iron in the magmatic-hydrothermal fluid, leading to precipitation of massive

  8. Calculation of the properties of the S3- radical anion and its complexes with Cu+ in aqueous solution (United States)

    Tossell, J. A.


    A species observed in aqueous sulfidic solutions at high T and P has recently been identified as the anion radical S3-, based on the Raman spectrum obtained in a hydrothermal diamond-anvil cell (Pokrovski and Dubrovinsky, 2011, Science, 331, 1052-1054). Such a species had not been expected to occur in such environments, although S3- as an component of lapis lazuli, other solids and even albite melt has been well studied (Winther et al., 1998; Reinen and Lindner, 1999; Arieli et al., 2004; Shnitko et al., 2008; Bacci et al., 2009). We have calculated the structures, energetics, vibrational and UV-visible spectra of S3- and several other similar species and confirm the species identification of Pokrovski and Dubrovinsky, although we are still somewhat concerned about the apparent lack of a third peak which we calculate to be present in the Raman spectrum of S3-. Our calculations indicate that the reaction: S6-2⇒2S3- in aqueous solution has a free energy change of +3 kcal/mol at 298 K and 1 atm pressure but -13 kcal/mol at 723 K and 1 atm pressure, consistent with the disappearance of disulfide species and the appearance of S3-at high T. Likewise, the free energy for the reaction: 2HS+SO4-2+H⇒S3-+.75O+2.5HO decreases from 44.1 to 19.0 kcal/mol between 298 and 723 K (again at 1 atm). This is consistent with the decrease in concentrations of SH- and SO4-2 and the formation of S3- observed by Pokrovski and Dubrovinski over this temperature range. The corresponding log K values are in semiquantitative agreement with those found by Pokrovski and Dubrovinsky. The main contribution to these changes in reaction free energy with temperature come from the VRT (vibrational-rotational-translational) contribution to the gas-phase free energy, while the hydration free energy difference changes little. Calculation of 34S-32S isotopic fractionations for S3- at 298 K give δ values of around +4.3% relative to H2S, a value intermediate between that of S3 and S3-2. Calculated free

  9. Mineralogical and geochemical characteristics of the Archaean LCT pegmatite deposit Cattlin Creek, Ravensthorpe, Western Australia (United States)

    Bauer, Matthias; Dittrich, Thomas; Seifert, Thomas; Schulz, Bernhard


    The LCT (lithium-cesium-tantalum) pegmatite Cattlin Creek is located about 550 km ESE of Perth, Western Australia. The complex-type, rare-element pegmatite is hosted in metamorphic rocks of the Archaean Ravensthorpe greenstone belt, which constitutes of the southern edge of the Southern Cross Terranes of the Yilgarn Craton. The deposit is currently mined for both lithium and tantalum by Galaxy Resources Limited since 2010. The pegmatitic melt intruded in a weak structural zone of crossing thrust faults and formed several pegmatite sills, of which the surface nearest mineralized pegmatite body is up to 21 m thick. The Cattlin Creek pegmatite is characterized by an extreme fractionation that resulted in the enrichment of rare elements like Li, Cs, Rb, Sn and Ta, as well as the formation of a vertical zonation expressed by distinct mineral assemblages. The border zone comprises a fine-grained mineral assemblage consisting of albite, quartz, muscovite that merges into a medium-grained wall zone and pegmatitic-textured intermediate zones. Those zones are manifested by the occurrence of megacrystic spodumene crystals with grain sizes ranging from a couple of centimeters up to several metres. The core zone represents the most fractionated part of the pegmatite and consists of lepidolite, cleavelandite, and quartz. It also exhibits the highest concentrations of Cs (0.5 wt.%), Li (0.4 wt.%), Rb (3 wt.%), Ta (0.3 wt.%) and F (4 wt.%). This zone was probably formed in the very last crystallization stage of the pegmatite and its minerals replaced earlier crystallized mineral assemblages. Moreover, the core zone hosts subordinate extremely Cs-enriched (up to 13 wt.% Cs2O) mineral species of beryl. The chemical composition of this beryl resamples that of the extreme rare beryl-variety pezzotaite. Other observed subordinate, minor and accessory minerals comprise tourmaline, garnet, cassiterite, apatite, (mangano-) columbite, tantalite, microlite (Bi-bearing), gahnite, fluorite

  10. Crystallization conditions and petrogenesis of the lava dome from the ˜900 years BP eruption of Cerro Machín Volcano, Colombia (United States)

    Laeger, Kathrin; Halama, Ralf; Hansteen, Thor; Savov, Ivan P.; Murcia, Hugo F.; Cortés, Gloria P.; Garbe-Schönberg, Dieter


    The last known eruption at Cerro Machín Volcano (CMV) in the Central Cordillera of Colombia occurred ˜900 years BP and ended with the formation of a dacitic lava dome. The dome rocks contain both normally and reversely zoned plagioclase (An24-54), unzoned and reversely zoned amphiboles of dominantly tschermakite and pargasite/magnesio-hastingsite composition and olivine xenocrysts (Fo = 85-88) with amphibole/clinopyroxene overgrowth, all suggesting interaction with mafic magma at depth. Plagioclase additionally exhibits complex oscillatory zoning patterns reflecting repeated replenishment, fractionation and changes in intrinsic conditions in the magma reservoir. Unzoned amphiboles and cores of the reversely zoned amphiboles give identical crystallization conditions of 910 ± 30 °C and 360 ± 70 MPa, corresponding to a depth of about 13 ± 2 km, at moderately oxidized conditions (f = +0.5 ± 0.2 ΔNNO). The water content in the melt, calculated based on amphibole chemistry, is 7.1 ± 0.4 wt.%. Rims of the reversely zoned amphiboles are relatively enriched in MgO and yield higher crystallization temperatures (T = 970 ± 25 °C), slightly lower melt H2O contents (6.1 ± 0.7 wt.%) and overlapping pressures (410 ± 100 MPa). We suggest that these rims crystallized following an influx of mafic melt into a resident magma reservoir at mid-crustal depths, further supported by the occurrence of xenocrystic olivine. Crystallization of biotite, albite-rich plagioclase and quartz occurred at comparatively low temperatures (probably rock chemistry of the CMV lava dome dacites is homogenous. They have elevated (La/Nb)N ratios of 3.8-4.5, typical for convergent margin magmas, and display several geochemical characteristics of adakites. Both Sr and Nd isotope compositions (87Sr/86Sr ˜0.70497, 143Nd/144Nd ˜0.51267) are among the most radiogenic observed for the Northern Volcanic Zone of the Andes. They are distinct from oceanic crust that has been subducted in the region

  11. Fault-zone structure and weakening processes in basin-scale reverse faults: The Moonlight Fault Zone, South Island, New Zealand (United States)

    Alder, S.; Smith, S. A. F.; Scott, J. M.


    The >200 km long Moonlight Fault Zone (MFZ) in southern New Zealand was an Oligocene basin-bounding normal fault zone that reactivated in the Miocene as a high-angle reverse fault (present dip angle 65°-75°). Regional exhumation in the last c. 5 Ma has resulted in deep exposures of the MFZ that present an opportunity to study the structure and deformation processes that were active in a basin-scale reverse fault at basement depths. Syn-rift sediments are preserved only as thin fault-bound slivers. The hanging wall and footwall of the MFZ are mainly greenschist facies quartzofeldspathic schists that have a steeply-dipping (55°-75°) foliation subparallel to the main fault trace. In more fissile lithologies (e.g. greyschists), hanging-wall deformation occurred by the development of foliation-parallel breccia layers up to a few centimetres thick. Greyschists in the footwall deformed mainly by folding and formation of tabular, foliation-parallel breccias up to 1 m wide. Where the hanging-wall contains more competent lithologies (e.g. greenschist facies metabasite) it is laced with networks of pseudotachylyte that formed parallel to the host rock foliation in a damage zone extending up to 500 m from the main fault trace. The fault core contains an up to 20 m thick sequence of breccias, cataclasites and foliated cataclasites preserving evidence for the progressive development of interconnected networks of (partly authigenic) chlorite and muscovite. Deformation in the fault core occurred by cataclasis of quartz and albite, frictional sliding of chlorite and muscovite grains, and dissolution-precipitation. Combined with published friction and permeability data, our observations suggest that: 1) host rock lithology and anisotropy were the primary controls on the structure of the MFZ at basement depths and 2) high-angle reverse slip was facilitated by the low frictional strength of fault core materials. Restriction of pseudotachylyte networks to the hanging-wall of the

  12. Petrology, geochemistry, and geochronology of trondhjemites from the Qori Complex, Neyriz, Iran (United States)

    Fazlnia, Abdolnaser; Schenk, Volker; van der Straaten, François; Mirmohammadi, Mirsaleh


    Metamorphism, magmatism, and thrusting were the result of subduction of Neotethys beneath the continental-margin arc of the Sanandaj-Sirjan shear zone (SSSZ) during the Mesozoic. The Qori metamorphic complex is a part of the southern SSSZ. Leuco-granitic (trondhjemitic) rocks crop out in the Qori metamorphic complex and are rare rock types in the SSSZ. These rocks have intruded into the marbles and garnet amphibolites, the highest grade metamorphic rocks of the Qori metamorphic complex, and in some outcrops, a transitional boundary between the amphibolites and the granitoids can be distinguished. The granitoids are granular in texture and consist of plagioclase (albite-oligoclase), quartz ± K-feldspar ±muscovite and subordinate garnet, spinel, rutile, and apatite which primarily occur as inclusions in the main phases. The peraluminous trondhjemitic rocks are enriched in Na 2O and SiO 2 and depleted in FeO, MgO, and CaO. Similarities with some trondhjemitic liquids produced through partial melting of amphibolites or hydrous basalts (i.e., low-Al 2O 3 content, less than 15 wt.%; low Ba, Sr, TiO 2, and Eu content, all with negative anomalies; moderately enriched LREEs and Y, and flat HREE patterns) suggest that the evolution of the parental magma was controlled by residual plagioclases during partial melting of a garnet amphibolite source. Concentrations of ferromagnesian elements, Mg, Fe, and Mn, are low, suggesting that the granitic rocks were not produced by high degrees of partial melting. Furthermore, they display low amounts of ferromagnesian components from the protolith (garnet amphibolite). This is supported by consideration of compatible elements, especially Cr, Ni and Ti (and the less robust HREE), which respectively show very high and high bulk partition coefficients for relatively small degrees (SHRIMP ages of the trondhjemite show magmatic ages of 147.4 ± 0.76 Ma, Volgian, Late Jurassic, and suggest that Neotethys began to subduct beneath the

  13. Secondary electron emission from lunar soil by solar wind type ion impact: Laboratory measurements (United States)

    Dukes, Catherine; Bu, Caixia; Baragiola, Raul A.


    Introduction: The lunar surface potential is determined by time-varying fluxes of electrons and ions from the solar wind, photoelectrons ejected by UV photons, cosmic rays, and micrometeorite impacts. Solar wind ions have a dual role in the charging process, adding positive charge to the lunar regolith upon impact and ejecting negative secondary electrons (SE). Electron emission occurs when the energy from the impacting ion is transferred to the solid, ionizing and damaging the material; electrons with kinetic energy greater than the ionization potential (band gap + electron affinity) are ejected from the solid[1].Experiment: We investigate the energy distribution of secondary electrons ejected from Apollo soils of varying maturity and lunar analogs by 4 keV He+. Soils are placed into a shallow Al cup and compressed. In-situ low-energy oxygen plasma is used to clean atmospheric contaminants from the soil before analysis[2]. X-ray photoelectron spectroscopy ascertains that the sample surface is clean. Experiments are conducted in a PHI 560 system (mirror electron energy analyzer (CMA) and μ-metal shield. The spectrometer is used to measure SE distributions, as well as for in situ surface characterization. A small negative bias (~5V) with respect to the grounded entrance grid of the CMA may be placed on the sample holder in order to expose the low energy cutoff.To measure SE energy distributions, primary ions rastered over a ~6 x 6 mm2 area are incident on the sample at ~40° relative to the surface normal, while SE emitted with an angle of 42.3°± 3.5° in a cone are analyzed.Results: The energy distribution of SE ejected from 4 keV He ion irradiation of albite with no bias applied shows positive charging of the surface. The general shape and distribution peak (~4 eV) are consistent with spectra for low energy ions on insulating material[1].Acknowledgements: We thank the NASA LASER program for support.References: [1]P. Riccardi, R. Baragiola et al. (2004); Surf

  14. Varena suite in the crystalline crust of the Southern Lithuania: implication to the genesis and mineralization (United States)

    Kirkliauskaite, Vaida; Motuza, Gediminas; Skipityte, Raminta


    Keywords: Lithuania, Proterozoic, Varena suite, rare earth elements, metasomatosis. Crystalline crust in Southern Lithuania is covered by 200-500 m thick sedimentary cover and is investigated by potential field mapping and drilling. It is composed by amphibolites (metabasalts), biotite-quartz-plagioclase gneisses (metapsammites and porphyry metadacite and metaandesite) of Orosirian period. Each lithology is predominant in alternating bands extended NNE-SSW. Supracrustals are metamorphosed on the level of amphibolite facies and migmatized. Intrusive rocks are represented by coeval rare bodies of gabbro, peridotite and widespread Calymmian granitic plutons. Varena suite comprises olivine, enstatite, diopside, olivine-magnetite, magnetite, apatite-bearing, and presumably also dolomite rocks. They form integrated bodies few sq. km large, concentrated in the ˜300 km2area extended in N-S direction.Bodies of particular rocks from Varena suite fixed in the boreholes are few tenths up to few hundred meters thick, except apatite-bearing rocks, forming decimeter up to meter scale lenses and veins. Rocks of Varena suite are affected by strong metasomatic alteration. Olivine is substituted by serpentine, and phlogopite, pyroxenes with amphibols (hornblende, actinolite, tremolite, rarely richterite). The country rocks (amphibolites, metaporphyres) also affected by alkaline (mainly sodic) metasomatosis manifested by formation of scapolite, albite, clynopyroxene (often sodic), phlogopite, carbonates. The mineralization of REE (up to 2759-3100 ppm of La and Ce respectively), Th, U, P hosted by monazite, apatite, allanite is spatially related to the Varena suite and some metasomatized supracrustals. The views on the genesis of Varena suite are contradicting. By various authors they are regarded as skarns, presuming metasomatic origin, as layered intrusions or products of alkaline and carbonatitic magmatism. In this presentation the genetic model is reviewed based on

  15. Reactivity of organic-rich sediment in seawater at 350°c, 500 bars: experimental and theoretical constraints and implications for the guaymas basin hydrothermal system (United States)

    Thornton, Edward C.; Seyfried, W. E., Jr.


    Hydrothermal alteration of organic-rich diatomaceous sediment by seawater was modelled experimentally at 350°C, 500 bars and seawater/sediment mass ratio of 3. The experiment was performed to assess the effect of organic matter reactivity on solution speciation and sediment alteration processes at an elevated temperature and pressure and provide requisite data to better understand the chemistry of hydrothermal fluids issuing from vents in the Guaymas Basin, Gulf of California. Seawater chemistry changed greatly during the experiment. In particular, Na, Mg and SO 4 decreased, while ∑ CO 2, ∑ NH 3, ∑ H 2S, SiO 2, Ca, K, H 2, CH 4 and heavy and base metals increased. Moreover, owing to the thermal alteration of sediment organic matter, organic acids, phenolic derivatives and phthlate were released to solution. Examination of solid alteration products revealed the effects of extensive dissolution and precipitation processes characterized by total elimination of diatoms and formation of cristobalite, quartz (?), pyrite, pyrrhotite, mixed layer chlorite/smectite and calcite. Plagioclase feldspar (An 40) recrystallized to a more albitic form owing to Na fixation and Ca cycling to calcite. A graphitic residue was also present in the products of the experiment. Mg and Na fixation reactions during the experiment generated significant H +, although the pH measured at 25°C was approximately 6.2. SO 4 reduction and thermal alteration and dissolution of organics, however, consume H + and are chiefly responsible for the near neutral pH for the overall reaction. Speciation calculations including ammine and acetate protonation reactions give a pH at experimental conditions of approximately 5.1, while mineral solubility relations involving virtually all alteration phases require a pH of 5.57 to 5.94. A near neutral pH at experimental conditions constrains the mobility of Fe, Mn, Zn, Cu and Ni, which existed in solution as chloro-complexes. Dissolved concentrations of Pb and

  16. Fluid-Dacite Interaction in the PACMANUS Subseafloor Hydrothermal System - Preliminary Results From Secondary Mineral Chemistry and Geochemical Modeling (United States)

    Yeats, C. J.; Bach, W.; Vanko, D. A.; Roberts, S.; Lackschewitz, K.; Paulick, H.


    During Ocean Drilling Program Leg 193, several holes (as deep as 386 meters below sea floor) intersected variably altered and veined dacites on Pual Ridge in the eastern Manus back-arc basin. The hydothermal alteration is complex and multi-stage, and includes pervasive alteration and alteration halos along anhydrite±pyrite±quartz veins. Our preliminary interpretation is that an early pervasive "chloritic" alteration (chlorite, chlorite/smectite, quartz, +/-albite, +/-magnetite) is overprinted locally by illite-pyrophyllite-anhydrite+/-diaspore alteration followed by silica (quartz and cristobalite) flooding. Two drill holes at Snowcap, a site of diffuse venting, reveal alteration profiles of strongly illite-pyrophyllite-anhydrite altered rocks in the shallow parts grading downwards into rocks that show dominant chloritic alteration. At Roman Ruins, a site of discrete venting, K-feldspar and illite-smectite mixed layer phases are abundant and magnetite is rare. K-feldspar appears to be part of the "chloritic" alteration assemblage. Anhydrite is locally abundant but generally less common than at Snowcap. There is a strong lateral heterogeneity in basement alteration as revealed by the differences between sites in the depths of cristobalite-quartz transition and the zones of prevailing alteration styles. Geochemical modeling suggests that the rocks have been altered at temperatures of about 250 to 300° C under variable fluid-to-rock ratios. While all the mineral assemblages are consistent with quartz/cristobalite saturation of the fluids, the formation of diaspore must be related to episodic interaction of the rocks with fluids highly undersaturated in quartz. The early stage of chloritic alteration represents interaction of the dacites with fluids of a fairly high pH ({>}4). In contrast, the occurrence of pyrophyllite and local diaspore suggests lower pH fluid ({hydrothermal stages. A zone of abundant alunite at 350 m deep in the basement at Snowcap may represent

  17. Influence of liquid structure on diffusive isotope separation in molten silicates and aqueous solutions (United States)

    Watkins, James M.; DePaolo, Donald J.; Ryerson, Frederick J.; Peterson, Brook T.


    Molecular diffusion in natural volcanic liquids discriminates between isotopes of major ions (e.g., Fe, Mg, Ca, and Li). Although isotope separation by diffusion is expected on theoretical grounds, the dependence on mass is highly variable for different elements and in different media. Silicate liquid diffusion experiments using simple liquid compositions were carried out to further probe the compositional dependence of diffusive isotopic discrimination and its relationship to liquid structure. Two diffusion couples consisting of the mineral constituents anorthite (CaAl 2Si 2O 8; denoted AN), albite (NaAlSi 3O 8; denoted AB), and diopside (CaMgSi 2O 6; denoted DI) were held at 1450 °C for 2 h and then quenched to ambient pressure and temperature. Major-element as well as Ca and Mg isotope profiles were measured on the recovered quenched glasses. In both experiments, Ca diffuses rapidly with respect to Si. In the AB-AN experiment, D Ca/ D Si ≈ 20 and the efficiency of isotope separation for Ca is much greater than in natural liquid experiments where D Ca/ D Si ≈ 1. In the AB-DI experiment, D Ca/ D Si ≈ 6 and the efficiency of isotope separation is between that of the natural liquid experiments and the AB-AN experiment. In the AB-DI experiment, D Mg/ D Si ≈ 1 and the efficiency of isotope separation for Mg is smaller than it is for Ca yet similar to that observed for Mg in natural liquids. The results from the experiments reported here, in combination with results from natural volcanic liquids, show clearly that the efficiency of diffusive separation of Ca isotopes is systematically related to the solvent-normalized diffusivity - the ratio of the diffusivity of the cation ( D Ca) to the diffusivity of silicon ( D Si). The results on Ca isotopes are consistent with available data on Fe, Li, and Mg isotopes in silicate liquids, when considered in terms of the parameter D cation/ D Si. Cations diffusing in aqueous solutions display a similar relationship

  18. Gamma-spectrometric surveys in differentiated granites. II: the Joaquim Murtinho Granite in the Cunhaporanga Granitic Complex, Parana, SE Brazil; Levantamentos gamaespectrometricos em granitos diferenciados. II: O exemplo do Granito Joaquim Murtinho, Complexo Granitico Cunhaporanga, Parana

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Francisco Jose Fonseca [Universidade Federal do Parana (UFPR), Curitiba, PR (Brazil). Dept. de Geologia. Lab. de Pesquisas em Geofisica Aplicada; Fruchting, Allan [Votorantim Metais, Sao Paulo, SP (Brazil)], e-mail:; Guimaraes, Gilson Burigo [Universidade Estadual de Ponta Grossa (UEPG), PR (Brazil). Dept. de Geociencias], e-mail:; Alves, Luizemara Soares [PETROBRAS S.A., Rio de Janeiro, RJ (Brazil)], e-mail:; Martin, Victor Miguel Oliveira; Ulbrich, Horstpeter Herberto Gustavo Jose [Universidade de Sao Paulo (USP), SP (Brazil). Inst. de Geociencias. Dept. de Mineralogia e Geotectonica], e-mail:, e-mail:


    Detailed mapping at the NW corner of the large Neo proterozoic Cunhaporanga Granitic Complex (CGC), Parana state, SE Brazil, redefined the Joaquim Murtinho Granite (JMG), a late intrusion in CGC with an exposed area of about 10 km{sup 2}, made up mainly by evolved 'alaskites' (alkali-feldspar leuco granites). This unit is in tectonic contact with the Neoproterozoic-Eocambrian volcano-sedimentary Castro Group, to the W, and is intrusive into other less evolved granitic units of the CGC to the E. Petrographically, JMG shows mainly mesoperthite and quartz, with subordinate amounts of altered micas and some accessory phases, mainly zircon. The equi to inequigranular granites are usually deformed with cataclastic textures, are often brecciated, and may have miarolitic structures. Formation of late albite, sericite, carbonate and hematite was caused by deuteric and hydrothermal alteration. A gamma-ray spectrometric survey at 231 stations which measured total counts (TC), Ueq K%, eU ppm and eTh ppm was used to construct several direct and derived maps. Compared to neighboring units the JMG has significant anomalies, especially in the TC, %K, eTh and eU maps, although the differences are less obvious in some derived maps. These evolved granites are enriched in these three elements. Geochemical behavior of K, Th and U is used to analyse the results observed in maps. Enhanced weathering under a subtropical climate with moderate to high average temperatures and heavy rainfall affects mainly feldspars and biotite, and may also destabilize most U and Th-bearing accessory phases. Th is most likely retained in restite minerals in soils, being relatively immobile, while part of U may migrate as uranyl ion in oxidizing media. K is especially affected by feldspar alteration to K-free clays (mainly kaolinite), and may be completely leached. Gamma-ray spectrometric methods are valid tools to study facies in granitic rocks, especially in those that are enriched in K, Th and U

  19. Long-Term CO2 Exposure Experiments - Geochemical Effects on Brine-Saturated Reservoir Sandstone (United States)

    Fischer, Sebastian; Zemke, Kornelia; Liebscher, Axel; Wandrey, Maren


    The injection of CO2 into deep saline aquifers is the most promising strategy for the reduction of CO2 emissions to the atmosphere via long-term geological storage. The study is part of the CO2SINK project conducted at Ketzin, situated 40 km west of Berlin. There, food grade CO2 has been pumped into the Upper Triassic Stuttgart Formation since June 2008. The main objective of the experimental program is to investigate the effects of long-term CO2 exposure on the physico-chemical properties of the reservoir rock. To achieve this goal, core samples from observation well Ktzi 202 have been saturated with synthetic brine and exposed to CO2 in high quality steel autoclaves at simulated reservoir P-T-conditions of 5.5 MPa and 40 ° C. The synthetic brine had a composition representative of the formation fluid (Förster et al., 2006) of 172.8 g/l NaCl, 8.0 g/l MgCl2×2H2O, 4.8 g/l CaCl2×2H2O and 0.6 g/l KCl. After 15 months, the first set of CO2-exposed samples was removed from the pressure vessels. Thin sections, XRD, SEM as well as EMP data were used to determine the mineralogical features of the reservoir rocks before and after the experiments. Additionally, NMR relaxation and MP was performed to measure poroperm and pore size distribution values of the twin samples. The analyzed samples are fine- to medium grained, moderately well- to well sorted and weakly consolidated sandstones. Quartz and plagioclase are the major components, while K-feldspar, hematite, white & dark mica, chlorite and illite are present in minor and varying amounts. Cements are composed of analcime, dolomite and anhydrite. Some samples show mm- to cm-scale cross-beddings. The laminae comprise lighter, quartz- and feldspar-dominated layers and dark-brownish layers with notably less quartz and feldspars. The results are consistent with those of Blaschke et al. (2008). The plagioclase composition indicates preferred dissolution of the Ca-component and a trend toward albite-rich phases or even pure

  20. Tectonic evolution of the East Junggar terrane, CAOB (United States)

    Xu, Xing-Wang


    reveal the following evidence: 1) The dioritic gneiss was metamorphosed from 2.52 Ga diorite at approximately 1.88 Ga, the magnetite quartzite interlayered with hornblende-plagioclase gneiss layers has an age of approximately 1.92 Ga, and the inherited zircons from the diorite TH4-6 contain three zircon populations with upper interceptages of approximately 3.06 Ga, 1.98 Ga and 1.89 Ga. These data indicate that the East Junggar terrane has Archean crust that formed at approximately 3.2-3.0 Ga and includes 2.52 Ga diorites and 4.0 Ga zircons and materials. 2) The Taheir tectonic window consists of metamorphic and deformed Ordovician volcanic rocks and granitic porphyries, Ordovician-Silurian granites and undeformed Silurian-Devonian granitic diorite, diorites and rhyolitic porphyries. The Ordovician volcanic rocks and granitic porphyries and Ordovician-Silurian granites in the Taheir tectonic window exhibit distinct features of Andean-type continental arc, such as enrichment in Pb, K and U, depletion in Nb, P and Ti, negative Eu anomalies, high La/Yb, Th/Yb and Ta/Yb values, a high proportion of dacite, rhyolite and andesite of the calc-alkaline series, massive contemporary granitic intrusions, mixtures of the juvenile material and >2.5 Ga crust, and extensive crystallization differentiation. These Ordovician volcanic rocks witnessed a series of tectonic events, including burial associated with the intrusion of 454-449 Ma granitic porphyries, underthrusting and subsidence to a depth in the middle crust associated with the intrusion of 443-432 Ma granites. The formation of albite-hornblende schists, hornblende-albite-quartz leptynites and amphibolites, the transformation from continental to continental island arc at approximately 432 Ma, the exhumation associated with the intrusion of 416-406 Ma diorites with geochemical signatures of continental island arc, and exhumation and erosion between 398 Ma and 390 Ma are also identified. The arc types that are associated with the

  1. Discovery of double-peaking potassic volcanic rocks in Langshan Group of the Tanyaokou hydrothermal-sedimentary deposit, Inner Mongolia, and its indicating significance

    Institute of Scientific and Technical Information of China (English)

    PENG; Runmin; ZHAI; Yusheng; WANG; Zhigang; HAN; Xuefeng


    It is revealed that the protolith of gray-light brown potash-feldspar-leucogranulites and granulites in the 2nd formation of the LG in Tanyaokou deposit are quartz kerotophyre of synsedimentary eruption based on the following facts and features: (1) The rocks look compact and homogeneous without obvious crystals with naked eyes; (2) they contain blastoporphyritic or glomeroporphyritic and blasto-crystalloclastic crystals consisting of quartz with wavy extinction and albite with obvious alteration and deformation; (3) they also contain radiated and fibrous blasto-microspherulitic texture and swallow-tailed bifurcate and blasto-hollow-skeleton crystal texture, representing the rapid cooling characteristic of the magma during submarine volcanic eruption; (4) the major chemical compositions of the rocks are: SiO2 = 70.80%―76.00%, K2O (4.83%―6.22%)>Na2O(2.78%―3.80%), and K2O+Na2O = 8.63%―9.00%; and (5) their petrochemical diagrams indicate that they are volcanic rocks. Together with the characteristic that they occur in the same sequence with potassic spilite (SiO2 = 46.12%―50.68%, K2O = 4.23%―5.93%>Na2O = 2.15%―3.14%, K2O+Na2O = 6.51%―8.08%), it can be confirmed that the volcanics occurring in the 2nd Formation of the LG in Tanyaokou district are double-peaking potassic volcanic rocks. The discovery, together with the tuffs with ore minerals and the distribution of lead isotopic as well as the value of Co/Ni of pyrites >1 showing the obvious endogenic metalization, can prove that the Tanyaokou deposit is an untypical SEDEX-type deposit formed in the extension fault basin in the Mesoproterozonic aulacogen of the northern margin of the North China Platform, and its metallogenesis is related to the synsedimentary volcanic activities and the hydrothermal exhalation, and both the ore-forming material source and volcanics came from mantle or lower crust. These facts mentioned above, together with the meta-volcanic rocks (double-peaking) found in the

  2. Composition, Temperature, and Pressure Dependence of the Phonon (Thermal) Conductivity of Silicate Geoliquids (United States)

    Tikunoff, Dane Michael

    which each oxygen atom is surrounded by two nearest neighbors of either Si or Al, is expected to possess a longer phonon mean free path, and thus higher conductivity, than the less polymerized liquid CaMgSi2O6, in which each oxygen atom, on average, is surrounded by only 4/3 nearest neighbors of Si. Simulation results for diopside melt at 2059+/-12 K and 0.04+/-0.14 GPa and albite melt at 2090+/-20 K and 0.20+/-0.23 GPa give values of k=1.143+/-0.004 W/m K and k=1.498+/-0.147 W/m K, respectively. Thus, this expectation based on empirical results has been faithfully captured by MD simulation. A modified Arrhenian expression was found to fit all liquids over the temperature and pressure range of the simulations (2000-4500 K and 0-30 GPa) reasonably well (correlation coefficient R2 ≈ 0.9). Activation energies are around 20 kJ/mol and activation volume is of order a few cm3/mol. A good correlation between the coordination numbers (CN) of Ca, Mg, Na, Al and Si around oxygen and by oxygen around the cations and thermal conductivity may be used semi-quantitatively to predict thermal conductivity in multi-component silicate liquids.

  3. Characterization and modes of occurrence of elements in feed coal and coal combustion products from a power plant utilizing low-sulfur coal from the Powder River Basin, Wyoming (United States)

    Brownfield, Michael E.; Cathcart, James D.; Affolter, Ronald H.; Brownfield, Isabelle K.; Rice, Cynthia A.; O'Connor, Joseph T.; Zielinski, Robert A.; Bullock, John H.; Hower, James C.; Meeker, Gregory P.


    The U.S. Geological Survey and the University of Kentucky Center for Applied Energy Research are collaborating with an Indiana utility company to determine the physical and chemical properties of feed coal and coal combustion products from a coal-fired power plant. The Indiana power plant utilizes a low-sulfur (0.23 to 0.47 weight percent S) and lowash (4.9 to 6.3 weight percent ash) subbituminous coal from the Wyodak-Anderson coal zone in the Tongue River Member of the Paleocene Fort Union Formation, Powder River Basin, Wyoming. Based on scanning electron microscope and X-ray diffraction analyses of feed coal samples, two mineral suites were identified: (1) a primary or detrital suite consisting of quartz (including beta-form grains), biotite, feldspar, and minor zircon; and (2) a secondary authigenic mineral suite containing alumino-phosphates (crandallite and gorceixite), kaolinite, carbonates (calcite and dolomite), quartz, anatase, barite, and pyrite. The primary mineral suite is interpreted, in part, to be of volcanic origin, whereas the authigenic mineral suite is interpreted, in part, to be the result of the alteration of the volcanic minerals. The mineral suites have contributed to the higher amounts of barium, calcium, magnesium, phosphorus, sodium, strontium, and titanium in the Powder River Basin feed coals in comparison to eastern coals. X-ray diffraction analysis indicates that (1) fly ash is mostly aluminate glass, perovskite, lime, gehlenite, quartz, and phosphates with minor amounts of periclase, anhydrite, hematite, and spinel group minerals; and (2) bottom ash is predominantly quartz, plagioclase (albite and anorthite), pyroxene (augite and fassaite), rhodonite, and akermanite, and spinel group minerals. Microprobe and scanning electron microscope analyses of fly ash samples revealed quartz, zircon, and monazite, euhedral laths of corundum with merrillite, hematite, dendritic spinels/ferrites, wollastonite, and periclase. The abundant calcium and

  4. Transmission Electron Microscopy of Itokawa Regolith Grains (United States)

    Keller, Lindsay P.; Berger, E. L.


    Introduction: In a remarkable engineering achievement, the JAXA space agency successfully recovered the Hayabusa space-craft in June 2010, following a non-optimal encounter and sur-face sampling mission to asteroid 25143 Itokawa. These are the first direct samples ever obtained and returned from the surface of an asteroid. The Hayabusa samples thus present a special op-portunity to directly investigate the evolution of asteroidal sur-faces, from the development of the regolith to the study of the effects of space weathering. Here we report on our preliminary TEM measurements on two Itokawa samples. Methods: We were allocated particles RA-QD02-0125 and RA-QD02-0211. Both particles were embedded in low viscosity epoxy and thin sections were prepared using ultramicrotomy. High resolution images and electron diffraction data were ob-tained using a JEOL 2500SE 200 kV field-emission scanning-transmission electron microscope. Quantitative maps and anal-yses were obtained using a Thermo thin-window energy-dispersive x-ray (EDX) spectrometer. Results: Both particles are olivine-rich (Fo70) with µm-sized inclusions of FeS and have microstructurally complex rims. Par-ticle RA-QD02-0125 is rounded and has numerous sub-µm grains attached to its surface including FeS, albite, olivine, and rare melt droplets. Solar flare tracks have not been observed, but the particle is surrounded by a continuous 50 nm thick, stuctur-ally disordered rim that is compositionally similar to the core of the grain. One of the surface adhering grains is pyrrhotite show-ing a S-depleted rim (8-10 nm thick) with nanophase Fe metal grains (<5 nm) decorating the outermost surface. The pyrrhotite displays a complex superstructure in its core that is absent in the S-depleted rim. Particle RA-QD02-0211 contains solar flare particle tracks (2x109 cm-2) and shows a structurally disordered rim 100 nm thick. The track density corresponds to a surface exposure of 103-104 years based on the track production rate


    Energy Technology Data Exchange (ETDEWEB)

    Billings, A; Tommy Edwards, T


    transition temperature measurement and TTT diagram development. The glass transition temperature (Tg) was measured using differential scanning calorimetry (DSC) and was recorded to be 443 {+-} 3 C. Using the previous TTT diagrams as guidance, subsamples of the glass were isothermally heat treated for 0.5 to 768 hours at temperatures between 400 C to 1100 C. Each of the 56 heat treated samples, along with quenched and centerline canister cooled (CCC) treated samples, were analyzed using Xray diffraction (XRD) and the PCT. Crystallization was detected only in samples treated at 600 C for more than 192 hours, and 700, 800, and 900 C for more than 48 hours. Phases crystallized were similar in composition if not the same as those found in the previous TTT studies. Six different crystalline phases were detected, including nepheline, acmite, lithium silicate, trevorite, krinovite, and albite. Overall, phases were spinel (iron) based, lithium metasilicate, sodium aluminosilicate or sodium transition metal silicate in composition. No new crystalline families were detected. Durability, as measured by the PCT, decreased when lithium silicate or nepheline crystals were present. Only one heat treated sample had a measured PCT response exceeding the benchmark EA glass, which was a sample treated at 600 C for 768 hours. During normal processing at the DWPF these conditions would be highly unlikely to occur, even in an extreme accident scenario. In order to continue to meet the requirements of the WCP, a simplified strategy is suggested for the generation of future TTT diagrams. A strategy has been developed that would require completing two more TTT diagrams for two averaged, future, predicted waste types. By creating diagrams for the resulting glass compositions of encompassing waste types, it will give insight to the crystallization regions possible for those averages. As discussed in the report, 'Initial MAR Assessments to Access the Impact of Al-Dissolution on DWPF Operating

  6. Compilation of kinetic data for geochemical calculations

    Energy Technology Data Exchange (ETDEWEB)

    Arthur, R.C. [Monitor Scientific, LLC., Denver, Colorado (United States); Savage, D. [Quintessa, Ltd., Nottingham (United Kingdom); Sasamoto, Hiroshi; Shibata, Masahiro; Yui, Mikazu [Japan Nuclear Cycle Development Inst., Tokai, Ibaraki (Japan). Tokai Works


    mineralogical and physical properties of the fracture must be homogeneous over a characteristic length that is greater than or equal to the equilibration length. If these conditions are met, calculations suggest local equilibrium would be a valid assumption in groundwater evolution models applied to the Kamaishi site if: it applies to reactions involving calcite, stilbite (assuming its dissolution / precipitation behavior is similar to that of heulandite), laumontite, albite and prehnite, but not quartz; Darcy flow velocities are relatively low (e.g., less than about 0.1 m yr-1), and it is based on the assumption that equilibrium corresponds to an uncertainty in the saturation index of 0.0{+-}0.4. If, however, actual reaction rates in the field are lower than expected, possibly because reactive surface areas are overestimated, the modeling approach may be inappropriate because it is probably unrealistic to assume that fracture mineralogy is homogeneous over fracture lengths exceeding a few meters or tens of meters. An analytical model of redox-front migration behavior based on the stationary-state approximation, and JNC's conceptual model of a natural events scenario involving the migration of oxidizing surface waters in fractures, suggests that oxidizing solutions could travel from the surface to the depth of a repository in crystalline rock within 400 to 50,000 years. These estimates are relatively short compared with time periods considered in safety assessments of repository performance, which suggests that time-dependent variations in the redox environment of both the near field and geosphere may need to be accounted for in these assessments. The flow velocities and concentrations of reducing minerals assumed in JNC's conceptual model may be overly conservative, however. (author)

  7. The origin of skarn beds, Ryllshyttan Zn-Pb-Ag + magnetite deposit, Bergslagen, Sweden (United States)

    Jansson, Nils F.; Allen, Rodney L.


    component. Subsequently, the calcareous Fe formations were subjected to post-depositional alteration by hydrothermal fluids, locally yielding more manganoan and magnesian assemblages. The Mn-alteration is manifested by lateral gradations from epidote-grandite-clinopyroxene±magnetite rocks into significantly more Mn-rich quartz-spessartine rocks and massive andradite rocks over distances of less than 10 cm within individual skarn beds. Magnesian alteration is manifested by the development of discordant zones of pargasite para-amphibolites and formation of stratiform pargasite rocks texturally similar to the interlaminated grandite-epidote-ferroan diopside rocks. The latter increase in abundance towards the Ryllshyttan deposit and are associated with pre-metamorphic/pre-tectonic K-Mg-Fe±Si alteration (now biotite-phlogopite-garnet-cordierite-pargasite rocks) that is related to base metal mineralization. The zone of Mn- and Mg-altered skarn beds extends beyond the zone of pervasive K-Mg-Fe±Si alteration around Ryllshyttan. This suggests that the skarn bed progenitors, or their sedimentary contacts against rhyolitic ash-siltstones, acted as conduits to outflowing hydrothermal fluids. The chemical and mineralogical imprint, imposed on affected beds by alteration, may serve as indicators of proximity to intense K-Mg-Fe±Si alteration envelopes around other base metal sulphide deposits in Bergslagen. The last recorded event comprised syn-tectonic veining of competent massive andradite skarn beds. The veins contain quartz-albite-epidote-ferroan diopside-actinolite assemblages.

  8. Geochemical and geochronological constraints on the genesis of Au-Te deposits at Cripple Creek, Colorado (United States)

    Kelley, K.D.; Romberger, S.B.; Beaty, D.W.; Pontius, J.A.; Snee, L.W.; Stein, H.J.; Thompson, T.B.


    The Cripple Creek district (653 metric tons (t) of Au) consists of Au-Te veins and disseminated gold deposits that are spatially related to alkaline igneous rocks in an Oligocene intrusive complex. Vein paragenesis includes quartz-biotite-K feldspar-fluorite-pyrite followed by base metal sulfides and telluride minerals. Disseminated deposits consist of microcrystalline native gold with pyrite that are associated with zones of pervasive adularia. New 40Ar/39Ar dates indicate that there was a complex magmatic and hydrothermal history. Relatively felsic rocks (tephriphonolite, trachyandesite, and phonolite) were emplaced into the complex over about 1 m.y., from 32.5 ?? 0.1 (1??) to 31.5 ?? 0.1 Ma. A younger episode of phonolite emplacement outside of the complex is indicated by an age of 30.9 ?? 0.1 Ma. Field relationships suggest that at least one episode of mafic and ultramafic dike emplacement occurred after relatively more felsic rocks and prior to the main gold mineralizing event. Only a single whole-rock date for mafic phonolite (which indicated a maximum age of 28.7 Ma) was obtained. However, constraints on the timing of mineralization are provided by paragenetically early vein minerals and K feldspar from the disseminated gold pyrite deposits. Early vein minerals (31.3 ?? 0.1-29.6 ?? 0.1 Ma) and K feldspar (29.8 ?? 0.1 Ma) from the Cresson disseminated deposit, together with potassically altered phonolite adjacent to the Pharmacist vein (28.8 and 28.2 ?? 0.1 Ma), suggest there was a protracted history of hydrothermal activity that began during the waning stages of phonolite and early mafic-ultramafic activity and continued, perhaps intermittently, for at least 2 m.y. Estimated whole-rock ??18O values of the alkaline igneous rocks range from 6.4 to 8.2 per mil. K feldspar and albite separates from igneous rocks have lead isotope compositions of 206Pb/204Pb = 17.90 to 18.10, 207Pb/204Pb = 15.51 to 15.53, and 208Pb/204Pb = 38.35 to 38.56. These isotopic

  9. 人工回灌条件下多组分溶质的反应迁移模拟%Fate and Transptort Simulation of Multi-Component Solute Under Artificial Recharge Conditions

    Institute of Scientific and Technical Information of China (English)

    苏小四; 谷小溪; 孟婧莹; 张文静; 王寒梅; 焦珣


    人工回灌技术在我国水资源管理中占据重要地位,但是其实施对地下水环境质量也造成了较大的影响.如何保障人工回灌条件下地下水环境质量的安全稳定性,已成为人工回灌技术发展的瓶颈.以上海市某人工回灌试验场为例,结合试验场的地质、水文地质勘探结果,以TOUGHREACT为数值模拟平台,模拟预测人工回灌条件下地下水中多组分溶质的迁移转化过程.模拟结果表明:地下水化学成分主要受混合作用、阳离子交换吸附作用及含水层矿物相溶解-沉淀作用等影响;含水介质中石英、白云石、钾长石、钠长石及蒙脱石发生溶解,方解石发生沉淀,伊利石与高岭石则先溶解后沉淀,但各矿物相反应量极其微弱;按不同压力方案回灌,水位恢复速率随压力增大而加快,但地下水中化学成分变化趋势几乎不受压力影响.%Groundwater recharge is an important way of water management strategies, including the natural recharge and artificial recharge. The study of groundwater recharge test as Baoshan District of Shanghai for example, with preliminary geological, hydrogeological exploration results, the purpose of filtering out the appropriate level of recharge (the fourth aquifer), establishing of recharge test hydrogeological conceptual model accorded to the aquifer permeability, hydraulic gradient, the main mineral composition and other basic properties. Then take TOUGHREACT for the numerical simulation platform, which software of non-isothermal multiphase flow and transforming simulation, to predict the quality of groundwater after recharging. The results show that chemical composition of groundwater is mainly affected by mixing, cation exchange adsorption and dissolution of aquifer minerals and so on; water-rock interaction process of quartz, dolomite, feldspar, albite Stone and montmorillonite dissolves,calcite precipitation, illite and kaolinite precipitation is first

  10. Mineralisation footprints and regional timing of the world-class Siguiri orogenic gold district (Guinea, West Africa) (United States)

    Lebrun, Erwann; Thébaud, Nicolas; Miller, John; Roberts, Malcolm; Evans, Noreen


    expressed as fracture zones of higher V3S vein density. A composite geochemical cross section across fracture zones from the Kosise deposit indicates that gold mineralisation in the Siguiri district is associated with enrichments in Ag, Au, As, Bi, Co, Mo, (Sb), S, Te and W relative to background. Geochemical variations associated with the ore shoots in the Siguiri district are consistent with petrographic observations and highlight an albite-carbonate-sulphide-sericite alteration. The fourth and last hydrothermal event is associated with the development of a late penetrative S4S cleavage during D4S deformation, which overprints all pre-existing hydrothermal features and is associated with the deposition of free gold, chalcopyrite and galena along fractures in V3A pyrite and V3B pyrite and arsenopyrite. Mineralogical and geochemical footprints as well as timing of the gold-mineralising events in the Siguiri district, when compared with other deposits of the West African Craton, highlight the synchronicity of gold mineralisation in Siguiri (syn-D3S and syn-D4S events) with other similar events in this part of the craton, such as the early Au-Sb-Bi-(Te-W) mineralisation at the Morila deposit in Southeast Mali. Our results support the hypothesis that late Eburnean-age gold mineralisation in the Siguiri district and in the West African Craton as a whole was polyphase.

  11. Timing, Formation and Mobility of Melano Granophyric Liquids in the Skaergaard Intrusion (United States)

    Larsen, R. B.; Sorensen, B.; Müller, A.


    Melano granophyric rocks are common throughout the cumulus stratigraphy of the Skaergaard intrusion. According to most studies, they comprise the end products of parental Skaergaard melt differentiation. Previous studies suggest that granophyre solidified at 690 to 720 C, long after the main body of the intrusion had solidified at c. 1040 C. However, much uncertainty associates T of formation of the melano granophyric melts. To approach this T we studied the mineralogy of melano granophyric chimney structures in the Middle Zone (MZ), and in gabbroic pegmatites from the Lower Zone, MZ and the Upper Zone (UZa-c). 19 vertical chimney structures perpendicularly intersect the cumulus layering in the upper third of MZ. Each chimney is 1-4 m in diameter and only the upper 2-3 m's are exposed. Melano granophyre also host the uppermost part of gabbroic pegmatite and occur in isolated clots (c. 0.1-0.3 m in diameter) in the cumulus stratigraphy 1-2 m above the pegmatites. Finally, there are several sub conformable bodies in the UZc where large proportions are composed of melano granophyre. The largest body is 50 m thick and can be followed laterally for > 200 m's. Whether in chimney structures, in clots or in gabbroic pegmatite, the melano granophyre feature the same mineral assemblage. Most conspicuously, they carry 5-20 cm black columnar crystals of ferro-hedenbergite with augite rims. In thin sections, the ferro-hedenbergite component form minute platelets much like ferro-hedenbergite in the UZc and, similarly, the texture is taken as evidence for the ferro-bustamite to ferro-hedenbergite inversion that occurs at c. 970 C after ferro-bustamite formed at c. 1040 C. Otherwise the melano granophyres are dominated by euhedral plagioclase, quartz, fayalite, hastingsitic hornblende, apatite and ilmenite and granophyric quartz, alkali feldspar and albite. With 700-2000 ppm, Zr is an important accessory that either form euhedral or skeletal crystals or symplectites. Titanium in

  12. Predictive modeling of CO2 sequestration in deep saline sandstone reservoirs: Impacts of geochemical kinetics

    Energy Technology Data Exchange (ETDEWEB)

    Balashov, Victor N.; Guthrie, George D.; Hakala, J. Alexandra; Lopano, Christina L.; Rimstidt, J. Donald; Brantley, Susan L.


    maximum CO{sub 2} sequestration, 34.5 kg CO{sub 2} per m{sup 3} of sandstone, is attained by 4000 years even though the system does not achieve chemical equilibrium until ~25,000 years. This maximum represents about 20% CO{sub 2} dissolved as CO{sub 2},aq, 50% dissolved as HCO{sub 3}{sup -}{sub ,aq}, and 30% precipitated as calcite. The extent of sequestration as HCO{sub 3}{sup -} at equilibrium can be calculated from equilibrium thermodynamics and is roughly equivalent to the amount of Na+ in the initial sandstone in a soluble mineral (here, oligoclase). Similarly, the extent of trapping in calcite is determined by the amount of Ca2+ in the initial oligoclase and smectite. Sensitivity analyses show that the rate of CO{sub 2} sequestration is sensitive to the mineral-water reaction kinetic constants between approximately 10 and 4000 years. The sensitivity of CO{sub 2} sequestration to the rate constants decreases in magnitude respectively from oligoclase to albite to smectite.

  13. La Hornblendita Ushuaia (Tierra del Fuego:: Petrografía, geoquímica y geocronología The Ushuaia Hornblendite (Tierra del Fuego: petrography, geochemistry and geochronology

    Directory of Open Access Journals (Sweden)

    R. D. Acevedo


    -piroxenites, diorites, gabbros, syenites and monzodiorites. The mineralogy of the most representative specimen shows that it is composed of hornblende and diopside as essential minerals, with biotite and potassic feldspar as minor constituents, and sphene, apatite, and opaque minerals (mainly magnetite, ilmenite, pyrite and chalcopyrite as accessories. Alteration processes include albitization, epidotization, chloritization and carbonatization, that represent substantial chemical changes that would affect any chemical classification of the rocks. Nevertheless, it is considered that the parental magma was of calc-alkaline Andean Type, related to the Andean Batholith, produced during regional subduction, and not in any way to an ophiolitic sequence. The calc-alkaline geochemistry is attributed to partial melting. In fact, the magma did not derive from primary mantle melts but came from evolved and contaminated mantle fluids that ascended toward crustal levels, thus favouring an assimilation process, in a magmatic arc setting. Potassium-argon whole-rock dating of one hornblendite sample gave an age of 113 ± 5 Ma

  14. El yacimiento de estaño Vil Achay, Catamarca The Vil Achay tin deposit of Catamarca, Argentina.

    Directory of Open Access Journals (Sweden)

    Ana S. Fogliata


    Full Text Available El yacimiento de estaño Vil Achay está ubicado en el flanco suroriental de la sierra de Fiambalá, provincia de Catamarca. Las rocas más antiguas aflorantes son anfibolitas pertenecientes al Gabro Fiambalá de edad ordovícica. Están intruidas por el granito El Salto de posible edad carbonífera. En las cercanías del contacto entre ambas unidades aflora un dique granítico emplazado en las anfibolitas, portador de la mineralización. La alteración hidrotermal en el dique granítico corresponde a albitización y greisenización. La mineralización (casiterita se encuentra diseminada en el dique. Existen sectores con mayor concentración de casiterita controlados por fracturas subverticales cerca del contacto oeste del dique. Se identificó la siguiente secuencia mineral: casiterita, magnetita, wolframita (escasa, calcopirita, pirita, covelina, calcosina, hematita, limonita, malaquita y azurita. El granito El Salto es meta a peraluminoso, postectónico, enriquecido en Rb, Nb, Y y Sn. La distribución de las tierras raras muestran fuerte fraccionamiento en tierras raras pesadas y relativo en tierras raras livianas. Tal fraccionamiento es indicativo de la actividad de los aniones de F en los fluidos mineralizantes. La gran actividad del F en los fluidos es responsable de la mineralización de Sn en greisen. Se propone que el depósito forma parte de un sistema tipo greisen abierto rico en F durante el estadio tardío magmático hidrotermal genéticamente relacionado con el granito El Salto.The Vil Achay tin deposit is located on the south-eastern flank of Sierra de Fiambalá in the province of Catamarca. The oldest exposed rocks are amphibolites of the Fiambalá Gabbro (Ordovician, intruded by the El Salto Granite of possible Carboniferous age. Within the amphibolites, near the contact between the two units, is a mineralized granitic dyke, exhibiting hydrothermal alteration (albitization and greisenization. Cassiterite is disseminated in the

  15. The brittle-viscous-plastic evolution of shear bands in the South Armorican Shear Zone (United States)

    Bukovská, Zita; Jeřábek, Petr; Morales, Luiz F. G.; Lexa, Ondrej; Milke, Ralf


    Shear bands are microscale shear zones that obliquely crosscut an existing anisotropy such as a foliation. The resulting S-C fabrics are characterized by angles lower than 45° and the C plane parallel to shear zone boundaries. The S-C fabrics typically occur in granitoids deformed at greenschist facies conditions in the vicinity of major shear zones. Despite their long recognition, mechanical reasons for localization of deformation into shear bands and their evolution is still poorly understood. In this work we focus on microscale characterization of the shear bands in the South Armorican Shear Zone, where the S-C fabrics were first recognized by Berthé et al. (1979). The initiation of shear bands in the right-lateral South Armorican Shear Zone is associated with the occurrence of microcracks crosscutting the recrystallized quartz aggregates that define the S fabric. In more advanced stages of shear band evolution, newly formed dominant K-feldspar, together with plagioclase, muscovite and chlorite occur in the microcracks, and the shear bands start to widen. K-feldspar replaces quartz by progressively bulging into the grain boundaries of recrystallized quartz grains, leading to disintegration of quartz aggregates and formation of fine-grained multiphase matrix mixture. The late stages of shear band development are marked by interconnection of fine-grained white mica into a band that crosscuts the original shear band matrix. In its extremity, the shear band widening may lead to the formation of ultramylonites. With the increasing proportion of shear band matrix from ~1% to ~12%, the angular relationship between S and C fabrics increases from ~30° to ~40°. The matrix phases within shear bands show differences in chemical composition related to distinct evolutionary stages of shear band formation. The chemical evolution is well documented in K-feldspar, where the albite component is highest in porphyroclasts within S fabric, lower in the newly formed grains within

  16. Predictive modeling of CO{sub 2} sequestration in deep saline sandstone reservoirs: Impacts of geochemical kinetics

    Energy Technology Data Exchange (ETDEWEB)

    Balashov, Victor N; Guthrie, George D; Hakala, J Alexandra; Lopano, Christina L. J.; Rimstidt, Donald; Brantley, Susan L


    maximum CO{sub 2} sequestration, 34.5 kg CO{sub 2} per m{sup 3} of sandstone, is attained by 4000 years even though the system does not achieve chemical equilibrium until ~25,000 years. This maximum represents about 20% CO{sub 2} dissolved as CO{sub 2},aq, 50% dissolved as HCO{sub 3}{sup -}{sub ,aq}, and 30% precipitated as calcite. The extent of sequestration as HCO{sub 3}{sup -} at equilibrium can be calculated from equilibrium thermodynamics and is roughly equivalent to the amount of Na+ in the initial sandstone in a soluble mineral (here, oligoclase). Similarly, the extent of trapping in calcite is determined by the amount of Ca2+ in the initial oligoclase and smectite. Sensitivity analyses show that the rate of CO{sub 2} sequestration is sensitive to the mineral-water reaction kinetic constants between approximately 10 and 4000 years. The sensitivity of CO{sub 2} sequestration to the rate constants decreases in magnitude respectively from oligoclase to albite to smectite.

  17. The giant Kalgoorlie Gold Field revisited

    Institute of Scientific and Technical Information of China (English)

    Noreen Mary Vielreicher; David Ian Groves; Neal Jesse McNaughton


    The Neoarchaean Kalgoorlie Gold Field contains the giant Golden Mile and world-class Mt Charlotte deposits, which have been the subject of much research for over 100 years. The Golden Mile deposit is a complex array of ductile to brittle vein and breccia lodes that are predominantly hosted in the highly-fractionated Golden Mile Dolerite sill. The Fimiston lodes comprise an array of narrow lodes that evolved broadly syn- to late-formation of the regional D2 NW-trending foliation. The lodes are charac-terized by pyrite veinlets and disseminations, quartz veinlets and breccias, and banded quartz-carbonate veins with sericite, carbonate, and pyrite-dominated alteration. Bonanza Green-Leader, or Oroya-style, lodes, with grades in excess of 1000 g/t Au, are similar to the Fimiston-style lodes, but are character-ized by abundant visible gold, native tellurium and more abundant telluride minerals within roscoelite-bearing alteration zones. The arguably structurally younger Mt Charlotte-style lodes are characterized by a pipe-shaped, coarse-grained quartz, carbonate and scheelite vein-stockwork with distinct vertically-zoned, carbonate-sericite-albite-pyrite ? pyrrhotite dominant alteration assemblages around veins within Unit 8 of the Golden Mile dolerite and porphyry dykes. The network of steep-and gently-dipping extension and shear fracture-fill veins are associated with NE-trending fault sets that cross cut the regional NW-trend. The deposit area is intruded by swarms of porphyry dykes, including syn-volcanic mafic dykes, early and volumetrically most significant c. 2.67 Ga feldspar-phyric porphyry dykes, as well as later c. 2.66‒2.65 Ga calc-alkaline hornblende-phyric dykes associated with younger c. 2.65‒2.64 Ga lamprophyre dykes. All post-volcanic dykes have similar orientations to the Fimiston lodes. The feldspar dykes are clearly overprinted by all styles of mineralization, although the relationship between hornblende-phyric and lamprophyre dykes and gold

  18. Geology of the Stroudsburg quadrangle and Adjacent areas, Pennsylvania--New Jersey (United States)

    Epstein, Jack Burton


    structures, including the prominent regional cleavage, were produced during the late Paleozoic Appalachian orogeny and are superimposed upon larger Taconic folds and faults. Field relations and microscopic study suggest that the regional cleavage in the Stroudsburg area is due to laminar flow of pelitic material along cleavage folia accompanied by mechanical reorientation of platy and elongate minerals and neocrystallization of mica, quartz, chlorite, and probably albite. Numerous lines of evidence point to the conclusion that cleavage developed after the rock was indurated and formed at, and Just below, conditions of low-grade metamorphism. Intensity of cleavage development increases to the southeast across the area. Second-generation slip cleavage, also believed to be Appalachian in age, formed by mechanical reorientation of minerals as well as by limited new mineral growth. The topography had a profound effect on the direction of movement of the Wisconsin glacier, as well as the manner of its retreat and the deposits that were formed. Till and stratified drift of Wisconsin age and till of Illinoian(?) age are common in the area. Wisconsin deglaciation occurred by northeastward retreat and by stagnation. A conspicuous terminal moraine marks the limit of Wisconsin ice movement. Lake Sciota was dammed between the retreating ice, the moraine, and the surrounding ridges north of Godfrey Ridge. Several deltas mark ice stand positions during the retreat of the ice. Lake-bottom and kame deposits are locally common in Cherry Valley. South of Kittatinny Mountain, on the other hand, melt water was freely discharged to the south. The wind and water gaps in the Stroudsburg area (including Delaware Water Gap and Wind Gap) are structurally controlled; specifically they are located where folds die out in short distances, where folding is locally more intense, or where resistant rocks dip steeply and have a narrow width of outcrop. This conclusion is contrary to

  19. A hot spring in granite of the Western Tianshan, China

    Energy Technology Data Exchange (ETDEWEB)

    Bucher, Kurt [Institute of Mineralogy, Albertstr.23 b, D-79104 Freiburg (Germany)], E-mail:; Zhang Lifei [School of Earth and Space Sciences, Peking University, Beijing, 100871 (China); Stober, Ingrid [Institute of Mineralogy, Albertstr.23 b, D-79104 Freiburg (Germany)


    . Sodium chloride is stored in fluid and solid inclusions in the granite, which have been introduced to quartz by ductile shearing and faulting related to ongoing orogenesis. The hot water remobilizes the salt that is continuously liberated by the tectonic deformation. Water-granite interaction contributes a thenardite-component (Na{sub 2}SO{sub 4}) to the major element composition by albite dissolution in H{sub 2}SO{sub 4}. The water-rock interaction along faults and fractures transforms and alters Muza granite to a low-temperature epigranite.

  20. Sedimentary carbonate-hosted giant Bayan Obo REE-Fe-Nb ore deposit of Inner Mongolia, China; a cornerstone example for giant polymetallic ore deposits of hydrothermal origin (United States)

    Chao, E.C.T.; Back, J.M.; Minkin, J.A.; Tatsumoto, M.; Junwen, Wang; Conrad, J.E.; McKee, E.H.; Zonglin, Hou; Qingrun, Meng; Shengguang, Huang


    Detailed, integrative field and laboratory studies of the textures, structures, chemical characteristics, and isotopically determined ages and signatures of mineralization of the Bayan Obo deposit provided evidence for the origin and characteristics favorable for its formation and parameters necessary for defining giant polymetallic deposits of hydrothermal origin. Bayan Obo is an epigenetic, metasomatic, hydrothermal rare earth element (REE)-Fe-Nb ore deposit that is hosted in the metasedimentary H8 dolostone marble of the Middle Proterozoic Bayan Obo Group. The metasedimentary sequence was deposited on the northern continental slope of the North China craton. The mine area is about 100 km south of the suture marking Caledonian subduction of the Mongolian oceanic plate from the north beneath the North China craton. The mineralogy of the deposit is very complex, consisting of more than 120 different minerals, some of which are epigenetic minerals introduced by hydrothermal solutions, and some of which are primary and secondary metamorphic minerals. The major REE minerals are monazite and bastnaesite, whereas magnetite and hematite are the dominant Fe-ore minerals, and columbite is the most abundant Nb mineral. Dolomite, alkali amphibole, fluorite, barite, aegirine augite, apatite, phlogopite, albite, and microcline are the most widespread gangue minerals. Three general types of ores occur at Bayan Obo: disseminated, banded, and massive ores. Broad zoning of these ore types occurs in the Main and East Orebodies. Disseminated ores are in the outermost zone, banded ores are in the intermediate zone, and massive ores are in the cores of the orebodies. On the basis of field relations, host rocks, textures, structures, and mineral assemblages, many varieties of these three types of ores have been recognized and mapped. Isotopic dating of monazite, bastnaesite, aeschynite, and metamorphic and metasomatic alkali amphiboles associated with the deposit provides constraints

  1. The origin of life near deep-sea hydrothermal systems during the Cambrian explosion: data from the Kyzyl Tashtyg sulphide deposit (Central Asia) (United States)

    Simonov, Vladimir; Terleev, Alexander; Safonova, Inna; Kotlyarov, Alexey; Stupakov, Sergey; Tokarev, Dmitry


    On Earth the solar radiation and the hydrothermal circulation both affect life evolution. Recent extensive studies of the World Ocean have shown that the biodiversity of Earth is linked with hydrothermal activity on the oceanic floor. These deep-sea ecosystems use chemical energy, not solar radiation. In the last quarter of the XX century, a new type of hydrothermal systems, so-called black smokers, was discovered in mid-oceanic ridges. As black smokers form sulfide ores and are surrounded by abundant bio-oases or symbioses, identification of their analogues in ancient orogenic belts is necessary for studying life origin and evolution. Of special importance are problems of life associated with deep-sea hydrothermal systems acted at the Precambrian-Cambrian boundary - the time of Cambrian explosion (Maruyama et al., 2013). During that explosion life significantly evolved and diversified due to dramatic changes of Earth's environment. Consequently, the early Cambrian - late Precambrian Kyzyl Tashtyg sulphide deposit of East Tuva in the Central Asian Orogenic Belt is of special interest. This deposit was formed on the bottom of ancient back-arc deep-sea basin as a result of black smoker hydrothermal activity and is hosted by volcanogenic-sedimentary rocks altered by the high temperature solutions. The altered Kyzyl Tashtyg basalts have an amygdules (filled by albite, epidote and carbonates), contain brown-green microfossils, often attached to their walls. The microfossils are thin tubes 5 to 25 microns in diameter and 500 microns long. This tubes are empty and have straight, curved or branching shape. Chemically, the tube material is close to epidote. In consideration of microscopic dimensions, simple morphology and similarity with modern tubular microorganisms, the studied tube-shaped microfossils can be related to cyanobacteria. Almost the same fossils, associated with oceanic basalt complexes, were described earlier (Furnes et al., 2007; Mcloughlin et al., 2007

  2. Organic petrology and geochemistry of mudrocks from the lacustrine Lucaogou Formation, Santanghu Basin, northwest China: Application to lake basin evolution (United States)

    Hackley, Paul C.; Fishman, Neil; Wu, Tao; Baugher, Gregory


    inertinite is present in the upper section, indicating greater terrestrial influx and consistent with higher quartz and plagioclase content (dominantly authigenic chalcedony and albite). Laminated mudstones in the upper section indicate anoxia prevented bioturbation from benthic grazing, also indicating stratified water column conditions. A decrease upsection in authigenic dolomite with reciprocal increase of ankerite/siderite is consistent with decreasing salinity, as is an overall decrease in gammacerane index values. These observations suggest evolution from a shallow, stratified evaporative (saline) setting to a deeper, stratified freshwater basin with higher water input during Lucaogou deposition. The evolution from an under-filled to balance-filled lake in Santanghu Basin is similar to Lucaogou deposition in Junggar Basin, suggesting similar tectonic and climatic controls. Paleoclimate interpretations from other researchers in this area suggested an evolution from semi-arid to humid conditions during the Roadian; we interpret that the evolution from an under-filled to balanced-filled lake seen in our data is in response to climate change, and may represent increased groundwater delivery to the Santanghu Basin.

  3. The Thermal Expansion Of Feldspars (United States)

    Hovis, G. L.; Medford, A.; Conlon, M.


    Hovis and others (1) investigated the thermal expansion of natural and synthetic AlSi3 feldspars and demonstrated that the coefficient of thermal expansion (α) decreases significantly, and linearly, with increasing room-temperature volume (VRT). In all such feldspars, therefore, chemical expansion limits thermal expansion. The scope of this work now has been broadened to include plagioclase and Ba-K feldspar crystalline solutions. X-ray powder diffraction data have been collected between room temperature and 925 °C on six plagioclase specimens ranging in composition from anorthite to oligoclase. When combined with thermal expansion data for albite (2,3,4) a steep linear trend of α as a function of VRT emerges, reflecting how small changes in composition dramatically affect expansion behavior. The thermal expansion data for five synthetic Ba-K feldspars ranging in composition from 20 to 100 mole percent celsian, combined with data for pure K-feldspar (3,4), show α-VRT relationships similar in nature to the plagioclase series, but with a slope and intercept different from the latter. Taken as a group all Al2Si2 feldspars, including anorthite and celsian from the present study along with Sr- (5) and Pb-feldspar (6) from other workers, show very limited thermal expansion that, unlike AlSi3 feldspars, has little dependence on the divalent-ion (or M-) site occupant. This apparently is due to the necessitated alternation of Al and Si in the tetrahedral sites of these minerals (7), which in turn locks the tetrahedral framework and makes the M-site occupant nearly irrelevant to expansion behavior. Indeed, in feldspar series with coupled chemical substitution it is the change away from a 1:1 Al:Si ratio that gives feldspars greater freedom to expand. Overall, the relationships among α, chemical composition, and room-temperature volume provide useful predictive tools for estimating feldspar thermal expansion and give insight into the controls of expansion behavior in

  4. 新疆冰达坂含金剪切带内组分分异及对金矿化的影响%Compositional Variation of the Bingdaban Goldbearing Shear Zone and Its Significance to the Gold Mineralization in Xinjiang

    Institute of Scientific and Technical Information of China (English)

    杨猛; 王居里; 王建其; 党飞鹏


    strain zone like ore offers better chemiphysical conditons to gold mineralization, such as higher Fe enrichment and expanding space like D, Ptype shearing fractures, where gold ore can locate. Meanwhile, due to the effect between alkali (especially Na) metasomatism and Si,K,Ca, compositions differentiate from the deeper layer to the lighter layer, which supplies stuff base for silication and quartzvein gold mineralization in the lighter layer with country rock alteration such as sericitization, carbonation, chloritization and so on. According to these findings, potash (especially Kf) alteration which may show as ore foot facies can be inferred under albitization alteration, which means there are some blind gold orebodies under both the deeper layer like Saridala tion belt. and the lighter layer like Wangfeng along the gold mineraliza

  5. 新疆南部祖母绿(绿柱石)成矿地质条件初探%Preliminary discussion of the the metailogenic conditions of emerald deposit, Southern Xinjiang, China

    Institute of Scientific and Technical Information of China (English)

    禹秀艳; 李甲平; 汪立今; 罗卫东; 石玉君; 陈勇; 陈俊华


    The emeralds of Xinjiang are good in quality, and the deposit has enormous potential yields of excellent quality emerald. This paper is mainly to analyze the geological characteristics of this deposit, including the regional geological features; mining and geological characteristics of ore body; ore mineralogi-cal characteristics of micro. The formation and distribution of emerald ore bodies found in Xinjiang are controlled by regional stratigraphy, magmatic, tectonic and other factors. Emerald (Beryl) Produced in the carbonaceous limestone, shale, calcite, calcite-quartz veinlets. Veins mostly were shaped by oblique veins, bedding pulse. Based on this study, according to samples collected, carrying on microscopic order of mineral assemblages and the formation of micro-mineralogy, mineralization process will be divided into three periods, namely before mineralization, mineralization period, after forming, obtained in the main ore minerals of the formation of calcite, quartz, albite, beryl, etc.. Through this research, the area emerald (beryl) exploration of important guiding significance.%新疆南部首次发现质量好的祖母绿(绿柱石),其成矿地质条件研究意义重大.本文主要对新疆南部祖母绿(绿柱石)矿的成矿地质条件进行初步探讨,包括区域地质特征、矿区及矿体地质特征、矿石显微矿物学特征等.发现新疆祖母绿矿体的形成和分布,受区内地层、岩浆、构造等多种因素和条件限制.祖母绿(绿柱石)多产于含碳质灰岩、页岩的方解石、方解石-石英细脉中,含祖母绿(绿柱石)矿脉多以斜交脉、顺层脉产出.在此研究基础上,根据所采集的样品,进行了显微矿物组合特征和生成顺序的微观矿物学研究,将成矿作用过程划分为三个期次,即成矿前、成矿期、成矿后.得出在成矿期形成的主要矿物为方解石、石英、钠长石、绿柱石等.通过上述研究,对该区祖母绿(绿柱石)找矿具有重要的指导意义.

  6. Geology and porphyry copper-type alteration-mineralization of igneous rocks at the Christmas Mine, Gila County, Arizona (United States)

    Koski, Randolph A.


    igneous rocks is progressively more alkaline and silicic from basalt to granodiorite. Early (Stage I) chalcopyrite-bornite (-molybdenite) mineralization and genetically related K-silicate alteration are centered on the Christmas stock. K-silicate alteration is manifested by pervasive hornblende-destructive biotitization in the stock, biotitization of basaltic volcanic wall rocks, and a continuous stockwork of K-feldspar veinlets and quartz-K-feldspar veins in the stock and quartz-sulfide veins in volcanic rocks. Younger (Stage II) pyrite-chalcopyrite mineralization and quartz-sericite-chlorite alteration occur in a zone overlapping with but largely peripheral to the zone of Stage I stockwork veins. Within the Christmas intrusive complex, K-silicate-altered rocks in the central stock are flanked east and west by zones of fracture-controlled quartz-sericite alteration and strong pyritization. In volcanic rocks quartz-chlorite-pyrite-chalcopyrite veins are superimposed on earlier biotitization and crosscut Stage I quartz-sulfide veins. Beyond the zones of quartz-sericite alteration, biotite rhyodacite porphyry dikes contain the propylitic alteration assemblage epidote-chlorite-albite-sphene. Chemical analyses indicate the following changes during pervasive alteration of igneous rocks: (1) addition of Si, K, H, S, and Cu, and loss of Fe 3+ and Ca during intense biotitization of basalt; (2) loss of Na and Ca, increase of Fe3+/Fe2+, and strong H-metasomatism during sericitization of quartz diorite; and (3) increase in Ca, Na, and Fe3+/Fe2+, and loss of K during intense propylitization of biotite rhyodacite porphyry dikes. Thorough biotitization of biotite granodiorite porphyry in the Christmas stock was largely an isochemical process. Fluid-inclusion petrography reveals that Stage I veins are characterized by low to moderate populations of moderate-salinity and gas-rich inclusions, and sparse but ubiquitous halite-bearing inclusions. Moderate-salinity an

  7. Solid oxide electrolysis cells - Performance and durability

    Energy Technology Data Exchange (ETDEWEB)

    Hauch, A.


    In this work H2 electrode supported solid oxide cells (SOC) produced at Risoe National Laboratory, DTU, have been used for steam electrolysis. Electrolysis tests have been performed at temperatures from 650AeC to 950AeC, p(H2O)/p(H2) from 0.99/0.01 to 0.30/0.70 and current densities from -0.25 A/cm2 to -2 A/cm2. The solid oxide electrolysis cells (SOEC) have been characterised by iV curves and electrochemical impedance spectroscopy (EIS) at start and end of tests and by EIS under current load during electrolysis testing. The tested SOCs have shown the best initial electrolysis performance reported in literature to date. Area specific resistances of 0.26 Oecm2 at 850AeC and 0.17 Oecm2 at 950AeC were obtained from electrolysis iV curves. The general trend for the SOEC tests was: 1) a short-term passivation in first few hundred hours, 2) then an activation and 3) a subsequent and underlying long-term degradation. The transient phenomenon (passivation/activation) was shown to be a set-up dependent artefact caused by the albite glass sealing with a p(Si(OH)4) of 1.10-7 atm, leading to silica contamination of the triple-phase boundaries (TPBs) of the electrode. The long-term degradation for the SOECs was more pronounced than for fuel cell testing of similar cells. Long-term degradation of 2%/1000 h was obtained at 850AeC, p(H2O)/p(H2) = 0.5/0.5 and -0.5 A/cm2, whereas the degradation rate increased to 6%/1000h at 950AeC, p(H2O)/p(H2) = 0.9/0.1 and -1.0 A/cm2. Both the short-term passivation and the long-term degradation appear mainly to be related to processes in the H2 electrode. Scanning electron microscopy micrographs show that only limited changes occur in the Ni particle size distribution and these are not the main degradation mechanism for the SOECs. Micro and nano analysis using energy dispersive spectroscopy in combination with transmission electron microscopy (TEM) and scanning TEM reveals that glassy phase impurities have accumulated at the TPBs as a result of

  8. Steatite and schist as contenders for the Global Heritage Stone Resource due to their importance in Brazil's natural stone built heritage (United States)

    Gilberto Costa, Antônio


    In Brazil, European natural stones, such as marble and limestone, were used as building material at historically important buildings and monuments, mainly in coastal cities, as well as in contemporary urban centers. However, in the country's central region, these Italian and Portuguese marbles and limestones were scarcely used. Instead, they were substituted for soapstone and several types of schist. As of 1755, the former was employed because of the ease with which it can be worked, essentially in the sculptural art and in the production of ornamental elements. Characterized by the presence of talc, steatite can feature other minerals such as serpentine, chlorite, carbonate, amphiboles, oxides like hematite and magnetite, and sulfites like pyrite, all in broadly variable amounts, which can result in modification of its technological properties (Volumetric Weight, Porosity, Water Absorption, Uniaxial Compression, Abrasion Resistance, Thermal Expansion etc.). In such rocks, talc content will be a decisive factor in their coloration. The higher its talc content is the clearer and softer the stone type will be, which ends up being known as talc stone. In such cases, the rock can display different hues of green, blue and gray. When compared to other rocks, texture patterns containing talc crystals, chlorite and carbonate contribute to low absorption and porosity for steatites. Schists were equally used at historical buildings in the Brazilian inland, especially in constructions in Minas Gerais towns, both in the production of structural elements such as bases, corners, pillars and foundations and in the creation of ornaments. Featuring different compositions, such rocks - which almost always occur interlayered with other ones such as quartzite - display coloration ranging from hues of gray to green to blue. They can be quartz-sericite-albite-chlorite schists featuring great or no amounts of carbonate, magnetite, epidote and tourmaline, sometimes with garnet, such as in

  9. The Western Cycladic Detachment System on Makronisos, Greece (United States)

    Loisl, Johannes; Lindner, Karoline; Huet, Benjamin; Grasemann, Bernhard; Rice, A. Hugh. N.; Soukis, Konstantinos; Schneider, David


    Makronisos, which lies 3 km east of the Attica port of Lavrion, is the northwesternmost part of the Western Cycladic archipelago. The Cyclades and adjacent part of Attica are dominated by Miocene low-angle detachments that developed during top-to-SSW crustal extension, forming the West Cycladic Detachment System. Although extension is well documented on the other Western Cycladic islands and in Attica, the geology of Makronisos is poorly known. The aim of this study is to provide data on the structural, microstructural and metamorphic evolution of Makronisos to resolve its tectonostratigraphic position and its relationships within the Cycladic realm. Most of Makronisos consists of grey, locally graphitic, pelitic schists and yellowish impure marbles, interlayed with blue-grey mylonitic marbles and quartzites, forming large-scale pinch-and-swell structures. Metabasites are present as small bodies along the east side of the island but are thicker and more continuous in the southeast. Petrography shows that metabasites usually contain blue amphiboles, although generally only as relicts after greenschist facies retrogression. Serpentinite has been found at two localities. The structurally highest level of the island consists of white-grey to pale-red ultramylonites up to 40 m thick. These mainly lie on the central ridge of the island, but, due to large-scale upright folding, also crop out along the east and west coasts. In several places, the ultramylonites overlie 1-2 m of foliated ultracataclasites derived from the footwall pelitic schists. Stretching lineations and macroscopic shear-criteria indicate a top-to-SSW shear-sense. Microstructural analyses consistently show the same shear-sense, indicated by shape and crystal preferred orientations, σ- and δ-clasts, mica-fish, rotated veins and SCC' structures. Deformation mechanisms observed in quartz (LT-bulging) and calcite (recrystallization) are evidence for deformation temperatures of c. 300°C. Albite

  10. Paragenesis and chemistry of multistage tourmaline formation in the sullivan Pb-Zn-Ag deposit, British Columbia (United States)

    Jiang, S.-Y.; Palmer, M.R.; Slack, J.F.; Shaw, D.R.


    Detailed petrographic study, scanning electron microscope imaging, and electron microprobe analyses of tourmalines from the Sullivan Pb-Zn-Ag massive sulfide deposit (British Columbia, Canada) document multiple paragenetic stages and large compositional variations. The tourmalines mainly belong to two common solid-solution series: dravite-schorl and dravite-uvite. Ca- and Fe-rich feruvite and alkali-deficient tourmalines are present locally. Products of tourmaline-forming stages include (from oldest to youngest): (1) rare Fe-rich dravite-schorl within black tourmalinite clasts in footwall fragmental rocks; (2) widespread Mg-rich, very fine grained, felted dravite in the footwall (the main type of tourmaline in the footwall tourmalinite pipe); (3) recrystallized, Fe-rich dravite-schorl (locally Ca-Fe feruvite) in the tourmalinite pipe, which preferentially occurs near postore gabbroic intrusions; (4) Mg-rich dravite or uvite associated with chlorite-pyrrhotite and chlorite-albite-pyrite-altered rocks in the shallow footwall and hanging wall; (5) discrete Mg-rich tourmaline grains associated with chlorite and discordant Mg-rich tourmaline rims which occur on disseminated Fe-rich schorl in the bedded Pb-Zn-Ag ores. The timing of rare Fe-rich schorl in the bedded ores is uncertain, but it most likely occurred during or between stages 2 and 3. The different paragenetic stages and their respective tourmaline compositions are interpreted in terms of a multistage evolution involving contributions from: (1) variable mixtures of synsedimentary, Fe-rich hydrothermal fluids and entrained seawater; (2) postore, Fe-rich, gabbro-related hydrothermal fluids; and (3) postore metamorphic reactions. Early synsedimentary, Fe-rich hydrothermal fluids which contained little or no entrained seawater formed Fe-rich black tourmalinite clasts locally in the footwall. The major type of tourmaline in the footwall tourmalinite pipe is Mg rich, recording seawater entrainment under high water

  11. Geochemical and technological characterization of clays of Corumbataí Formation, Paraná Basin, in the state of São Paulo, Brazil for the application in the ceramic industry. (United States)

    Christofoletti, Sergio Ricardo; Torres Moreno, Maria Margarita; Batezelli, Alessandro; Zanardo, Antenor


    The Corumbataí Formation is a geological unit of the Paraná Basin comprises a range of predominantly argillaceous facies. These clays are important from an economic point of view, because they represent important mineral deposits suppliers of raw materials for the ceramic industry in the production of ceramic tiles.The study presents preliminary results of a research that aims to study the clays municipalities Tambaú, Ferreira and Santa Rosa of Viterbo in the State of São Paulo for their application and diversification of ceramic products. The methodology used was based on a detailed description of facies using the methodology in principles of analysis of Basin Miall (1984), followed by mineralogical identification by X-ray Diffraction, chemical analysis of major elements by X-ray Fluorescence and technological tests ceramic. According to the geological surveys of mines studied through columnar sections were identified the following lithofacies from base to top: Massive, Laminated, Intercalated and Altered. The mineralogy present on these lithofacies is composed by minerals: quartz, microclineo, albite, calcite, dolomite and hematite and by clay minerals illite, kaolinite and montmorillonite. The quartz represents the mineral more present in diffraction and occurs with d001 of 3.33Å in all lithofacies studied. The illite clay mineral represents the most frequent in studied samples presenting d 001 10Å in three conditions (natural, heated and treated with ethylene glycol) in which the blade was subjected to the analysis of X-ray diffraction, the presence of kaolinite or montmorillonite occurs or not in samples. It was observed a increased frequency of some minerals in the lithofacies studied, carbonates (calcite and dolomite), hematite and feldspar occurring in the intermediate portions of the profile with a predominance in lithofacies Intercalated. The illita clay mineral occurs throughout the profile, but with greater frequency in the lithofacies Massive and

  12. Geochemical and Geochronologic Investigations of Zircon-hosted Melt Inclusions in Rhyolites from the Mesoproterozoic Pea Ridge IOA-REE Deposit, St. Francois Mountains, Missouri (United States)

    Watts, K. E.; Mercer, C. N.; Vazquez, J. A.


    Silicic volcanic and plutonic rocks of an eroded Mesoproterozoic caldera complex were intruded and replaced by iron ore, and cross-cut by REE-enriched breccia pipes (~12% total REO) to form the Pea Ridge iron-oxide-apatite-REE (IOA-REE) deposit. Igneous activity, iron ore formation, and REE mineralization overlapped in space and time, however the source of REEs and other metals (Fe, Cu, Au) integral to these economically important deposits remains unclear. Melt inclusions (MI) hosted in refractory zircon phenocrysts are used to constrain magmatic components and processes in the formation of the Pea Ridge deposit. Homogenized (1.4 kbar, 1000°C, 1 hr) MI in zircons from rhyolites ~600 ft (PR-91) and ~1200 ft (PR-12) laterally from the ore body were analyzed for major elements by EPMA and volatiles and trace elements (H2O, S, F, Cl, REEs, Rb, Sr, Y, Zr, Nb, U, Th) by SHRIMP-RG. Metals (including Cu, Au) will be measured in an upcoming SHRIMP-RG session. U-Pb ages, Ti and REE were determined by SHRIMP-RG for a subset of zircon spots adjacent to MI (1458 ± 18 Ma (PR-12); 1480 ± 45 Ma (PR-91)). MI glasses range from fresh and homogeneous dacite-rhyolite (65-75 wt% SiO2) to heterogeneous, patchy mixtures of K-spar and quartz (PR-12, 91), and more rarely mica, albite and/or anorthoclase (PR-91). MI are commonly attached to monazite and xenotime, particularly along re-entrants and zircon rims (PR-91). Fresh dacite-rhyolite glasses (PR-12) have moderate H2O (~2-2.5 wt%), Rb/Sr ratios (~8) and U (~5-7 ppm), and negative (chondrite-normalized) Eu anomalies (Eu ~0.4-0.7 ppm) (typical of rhyolites), whereas HREEs (Tb, Ho, Tm) are elevated (~2-3 ppm). Patchy K-spar and quartz inclusions (PR-12, 91) have flat LREE patterns, and positive anomalies in Tb, Ho, and Tm. One K-spar inclusion (PR-91) has a ~5-50 fold increase in HREEs (Tb, Dy, Ho, Er, Tm) and U (35 ppm) relative to other MI. U-Pb and REE analyses of its zircon host are not unusual (1484 ± 21 Ma); its irregular shape

  13. A new mineral species rossovskyite, (Fe3+,Ta)(Nb,Ti)O4: crystal chemistry and physical properties (United States)

    Konovalenko, Sergey I.; Ananyev, Sergey A.; Chukanov, Nikita V.; Rastsvetaeva, Ramiza K.; Aksenov, Sergey M.; Baeva, Anna A.; Gainov, Ramil R.; Vagizov, Farit G.; Lopatin, Oleg N.; Nebera, Tatiana S.


    A new mineral rossovskyite named after L.N. Rossovsky was discovered in granite pegmatites of the Bulgut occurrence, Altai Mts., Western Mongolia. Associated minerals are microcline, muscovite, quartz, albite, garnet of the almandine-spessartine series, beryl, apatite, triplite, zircon, pyrite, yttrobetafite-(Y) and schorl. Rossovskyite forms flattened anhedral grains up to 6 × 6 × 2 cm. The color of the mineral is black, and the streak is black as well. The luster is semi-metallic, dull. Mohs hardness is 6. No cleavage or parting is observed. Rossovskyite is brittle, with uneven fracture. The density measured by the hydrostatic weighing method is 6.06 g/cm2, and the density calculated from the empirical formula is 6.302 g/cm3. Rossovskyite is biaxial, and the color in reflection is gray to dark gray. The IR spectrum contains strong band at 567 cm-1 (with shoulders at 500 and 600 cm-1) corresponding to cation-oxygen stretching vibrations and weak bands at 1093 and 1185 cm-1 assigned as overtones. The reflection spectrum in visible range is obtained. According to the Mössbauer spectrum, the ratio Fe2+:Fe3+ is 35.6:64.4. The chemical composition is as follows (electron microprobe, Fe apportioned between FeO and Fe2O3 based on Mössbauer data, wt%): MnO 1.68, FeO 5.92, Fe2O3 14.66, TiO2 7.69, Nb2O5 26.59, Ta2O5 37.51, WO3 5.61, total 99.66. The empirical formula calculated on four O atoms is: {{Mn}}_{0.06}^{2 + } {{Fe}}_{0.21}^{2 + } {{Fe}}_{0.47}^{3 + } Ti0.25Nb0.51Ta0.43W0.06O4. The crystal structure was determined using single-crystal X-ray diffraction data. The new mineral is monoclinic, space group P2/ c, a = 4.668(1), b = 5.659(1), c = 5.061(1) Å, β = 90.21(1)º; V = 133.70(4) Å3, Z = 2. Topologically, the structure of rossovskyite is analogous to that of wolframite-group minerals. The crystal-chemical formula of rossovskyite is [(Fe3+, Fe2+, Mn)0.57Ta0.32Nb0.11][Nb0.40Ti0.25Fe0.18Ta0.11W0.06]O4. The strongest lines of the powder X-ray diffraction pattern

  14. Thermal structure of pumpellyite-actinolite facies regions in the Sanbagawa belt, Shikoku, SW Japan (United States)

    Sakaguchi, M.


    On the basis of the mineral assemblages of pelitic rocks, the Sanbagawa belt in Shikoku, SW Japan, has been divided, from low- to high-grade parts, into the chlorite, garnet, albite-biotite and oligoclase-biotite zones (Higashino, 1990). Also, the mineral assemblage of pumpellyite + actinolite + epidote + chlorite or epidote + actinolite + hematite + chlorite, which defines the pumpellyite-actinolite (PA) facies (e.g., Banno, 1998), is widely recognized in metabasites in the chlorite zone (e.g. Banno & Sakai, 1989). However, the detailed study on the PA facies regions has been done only in the Omoiji-Nagasawa area (Nakajima et al., 1977) and Asemigawa-Shirataki area (Nakajima, 1982) in central Shikoku, and thus, it is still hard to solve the regional thermal structure of the PA facies region. This study is aimed to reveal the thermal structure of the PA facies region of the Sanbagawa belt in Shikoku by analyzing the mineral assemblages and mineral chemistries of metabasites from the nine newly studied areas. The studied areas studied belong to the chlorite zone in the Oboke and Besshi units; the Oboke unit structurally underlay the Besshi unit. The mineral assemblages include pumpellyite + epidote + actinolite, epidote + actinolite _ hematite and epidote + Na-amphibole + actinolite + hematite. The metabasites from some areas involve Na-pyroxene-bearing assemblages, but the analyses of the Schreinemakers bundle of Tagiri et al. (1992) show that these assemblages do not define the Na-pyroxene-chlorite subfacies. As the low-grade metamorphic rocks do not have the hematite + pumpellyite paragenesis, its metamorphic temperature is estimated to be higher than the discontinuous reaction temperature of pumpellyite + hematite + quartz = epidote + actinolite + H2O, as shown by Nakajima et al. (1977). It is difficult to detect the difference in temperature in the PA facies regions by analyzing mineral assemblages. To detect the difference in temperature, and then to reveal

  15. UHP-Metamorphic Pyrope Quartzites From Dora Maira: Cathodoluminescence of Silica and Twinning of Coesite (United States)

    Schertl, H.; Medenbach, O.; Neuser, R. D.


    brownish-violet. Most interestingly these luminescence colours of quartz differ from those of quartz filling cracks (brown in colour, late generation of quartz) within the relic coesite crystals. The matrix quartz shows dark blue luminescence colours. In rare cases within the coesite/quartz inclusions in pyrope a mineral was observed exhibiting a bright brownish-yellow luminescence colour. Later studies revealed this mineral as chalcedony (Schertl et al., 2004, Fig. 1e), difficult to distinguish from quartz under the polarizing microscope because of their similar refractive indices and birefringences. Chalcedony as a low temperature phase was formed after cracking of the host pyrope. Twinning of coesite is reminiscent of polysynthethic plagioclase consisting of albite- and pericline-law individuals. Twinning of synthetic coesite was already reported by Ramsdell in 1955. He described (100)- and (021)-twins, that however, mainly derived from X-ray investigations because of the imperfect development of the run products. Further studies by Sclar et al. (1962) confirmed the occurrence of (021)-twins, Naka et al. (1975) provided evidence for (-121)- and (-233)-twins. Two respective types of lamellae in metamorphic coesites from Dora Maira were identified; their twin planes are intersecting each other with an angle of ca. 90°. The lamellae are twinned after (021) and (-101), the latter observed in natural coesite for the first time.

  16. Numerical modelling of gas-water-rock interactions in volcanic-hydrothermal environment: the Ischia Island (Southern Italy) case study. (United States)

    Di Napoli, R.; Federico, C.; Aiuppa, A.; D'Antonio, M.; Valenza, M.


    ). Overall, our model calculations satisfactorily reproduce the main chemical features of Ischia groundwaters. In the model runs, attainment of partial to complete equilibrium with albite and K-feldspar fixes the Na/K ratios of the model solutions at values closely matching those of natural samples. Precipitation of secondary phases, mainly clay minerals (smectite and saponite) and zeolites (clinoptilolite), during the reaction path is able to well explain the large Mg-depletions which characterise Ischia thermal groundwaters; while pyrite and troilite are shown to control sulphur abundance in aqueous solutions. SiO2(aq) contents in model simulations fit those measured in groundwaters and are being buffered by the formation of quartz polymorphs and Si-bearing minerals. Finally, our simulations are able to reproduce redox conditions and Fe-depletion trends of natural samples. We conclude that reaction path modelling is an useful tool for quantitative exploration of chemical process within volcano-hosted hydrothermal systems.

  17. Effects of glacial/post-glacial weathering compared with hydrothermal alteration - implications for matrix diffusion. Results from drillcore studies in porphyritic quartz monzodiorite from Aespoe SE Sweden

    Energy Technology Data Exchange (ETDEWEB)

    Landstroem, Ove [Studsvik Eco and Safety AB, Nykoeping (Sweden); Tullborg, Eva-Lena [Terralogica AB, Graabo (Sweden); Eriksson, Gunda; Sandell, Yvonne [Studsvik Nuclear AB, Nykoeping (Sweden)


    The effects of hydrothermal + subsequent low temperature alteration and glacial/post-glacial weathering have been studied in two cores of quartz monzodiorite. One core (YA 1192) was drilled into the hydrothermally altered wall rock of a water-conducting fracture exposed at 170 m depth in the access tunnel to the Aespoe Hard Rock Laboratory. The other one (Bas 1) was drilled from an outcrop with a glacially polished surface, 1 km north of the YA 1192 site. Both drill cores were sectioned into mm-thick slices perpendicular to the core axis. The fracture filling of the YA 1192 core, the weathered surface of the BAS 1 core and the different slices were analysed for major and trace elements and isotopes of U and Th. The altered zone of the YA 1192 core extends to approx. 2.5 cm from the fracture surface. The alteration (mainly plagioclase {yields} albite + sericite + epidote) has resulted in a higher porosity and formation of sorbing secondary minerals (e.g. sericite), favouring matrix diffusion. Increased Br concentrations in the altered zone are indicative of saline water in pores and micro fractures i.e. the presence of a diffusion medium. 234U/238U activity ratios > 1 and increased Cs in the altered zone are then interpreted as diffusion of U and Cs from fracture groundwater and subsequent sorption. The U migration is geologically recent (< 1 Ma). The 2.5 cm altered zone (corresponding to the zone of active matrix diffusion) significantly exceeds the visible red staining zone (0.5 cm) caused by hematite/FeOOH micrograins, emphasizing the need of microscopy to identify zones of alteration. The conspicuous weathering at the BAS 1 site is confined to a narrow rim of the bedrock surface (approx. 0.2-0.5 cm thick). Mass balance calculations for this rim (based on immobility of K) indicate that mechanical erosion has dominated over chemical dissolution processes (is roughly 10 times greater). The chemical weathering has affected mainly plagioclase and chlorite resulting

  18. The Itataia phosphate-uranium deposit (Ceará, Brazil) new petrographic, geochemistry and isotope studies (United States)

    Veríssimo, César Ulisses Vieira; Santos, Roberto Ventura; Parente, Clóvis Vaz; Oliveira, Claudinei Gouveia de; Cavalcanti, José Adilson Dias; Nogueira Neto, José de Araújo


    The Itataia phosphate-uranium deposit is located in Santa Quitéria, in central Ceará State, northeastern Brazil. Mineralization has occurred in different stages and involves quartz leaching (episyenitization), brecciation and microcrystalline phase formation of concretionary apatite. The last constitutes the main mineral of Itatiaia uranium ore, namely collophane. Collophanite ore occurs in massive bodies, lenses, breccia zones, veins or episyenite in marble layers, calc-silicate rocks and gneisses of the Itataia Group. There are two accepted theories on the origin of the earliest mineralization phase of Itataia ore: syngenetic (primary) - where the ore is derived from a continental source and then deposited in marine and coastal environments; and epigenetic (secondary) - whereby the fluids are of magmatic, metamorphic and meteoric origin. The characterization of pre- or post-deformational mineralization is controversial, since the features of the ore are interpreted as deformation. This investigation conducted isotopic studies and chemical analyses of minerals in marbles and calc-silicate rocks of the Alcantil and Barrigas Formations (Itataia Group), as well as petrographic and structural studies. Analysis of the thin sections shows at least three phosphate mineral phases associated with uranium mineralizaton: (1) A prismatic fluorapatite phase associated with chess-board albite, arfvedsonite and ferro-eckermannite; (2) a second fluorapatite phase with fibrous radial or colloform habits that replaces calcium carbonate in marble, especially along fractures, with minerals such as quartz, chlorite and zeolite also identified in calc-silicate rocks; and (3) an younger phosphate phase of botryoidal apatite (fluorapatite and hydroxyapatite) related with clay minerals and probably others calcium and aluminum phosphates. Detailed isotopic analysis carried out perpendicularly to the mineralized levels and veins in the marble revealed significant variation in isotopic

  19. Axial Belt Provenance: modern river sands from the core of collision orogens (United States)

    Resentini, A.; Vezzoli, G.; Paparella, P.; Padoan, M.; Andò, S.; Malusà, M.; Garzanti, E.


    Collision orogens have a complex structure, including diverse rock units assembled in various ways by geodynamic processes. Consequently, orogenic detritus embraces a varied range of signatures, and unravelling provenance of clastic wedges accumulated in adjacent foreland basins, foredeeps, or remnant-ocean basins is an arduous task. Dickinson and Suczek (1979) and Dickinson (1985) recognized the intrinsically composite nature of orogenic detritus, but did not attempt to establish clear conceptual and operational distinctions within their broad "Recycled Orogenic Provenance". In the Alpine and Himalayan belts, the bulk of the detritus is produced by focused erosion of the central backbone of the orogen, characterized by high topography and exhumation rates (Garzanti et al., 2004; Najman, 2006). Detritus derived from such axial nappe pile, including slivers of thinned continental-margin lithosphere metamorphosed at depth during early collisional stages, has diagnostic general features, which allows us to define an "Axial Belt Provenance" (Garzanti et al., 2007). In detail, "Axial Belt" detrital signatures are influenced by metamorphic grade of source rocks and relative abundance of continental versus oceanic protoliths, typifying distinct subprovenances. Metasedimentary cover nappes shed lithic to quartzolithic detritus, including metapelite, metapsammite, and metacarbonate grains of various ranks; only amphibolite-facies metasediments supply abundant heavy minerals (e.g., almandine garnet, staurolite, kyanite, sillimanite, diopsidic clinopyroxene). Continental-basement nappes shed hornblende-rich quartzofeldspathic detritus. Largely retrogressed blueschist to eclogite-facies metaophiolites supply albite, metabasite and foliated antigorite-serpentinite grains, along with abundant heavy minerals (epidote, zoisite, clinozoisite, lawsonite, actinolitic to barroisitic amphiboles, glaucophane, omphacitic clinopyroxene). Increasing metamorphic grade and deeper

  20. The general description of major ion concentrations in groundwater of Latvia (United States)

    Kalvāns, A.; Delina, A.


    Latvia is situated at the North central part of the Baltic sedimentary basin where the crystalline basement is found in depth between 0.6 to 2 km. Three large aquifer complexes with distinct chemical composition of groundwater are identified: the stagnant water exchange zone where Na-Ca-Cl brine is found; the slow water exchange zone where Na-Ca-Cl-SO4 brackish water is found and active water exchange zone where the freshwater resides. These are separated by distinct regional aquicludes. The composition of the Cl- dominated brines at the base of sedimentary basin is characterised by shift from Na+ towards Ca++ as dominant cation, partially associated with depth of the aquifer and the strength of the brine. The concentration of SO4-- here is inversely linked to the concentration of Ca++ and, according to geochemical modelling, often is close to the solubility limit of the gypsum. The major ion concentrations in the E and W part of the territory are rather different. Therefore two different initial sources of the formation brine were suggested. Alternatively the observations can be explained by different thermal histories of different parts of the basin, affecting the rate of albitization - exchange of the Na for Ca in the solution due to water-rock interaction. The groundwater composition in the slow exchange zone can be nicely explained by the mixing of freshwater and brine residing deeper in the presence of gypsum during some but no all stages of mixing. In some shallow parts of the zone still bound by the Narva regional aquiclude freshwater is found. The question is posted - could this be a paleogroundwater originating from the extensive continental glaciations that override the territory several times during the Pleistocene? Initial isotope studies presented elsewhere seems to give negative answer to this question. The active water exchange zone is characterised by fresh Ca-Mg-HCO3 water with exceptions in cases where gypsum are abundant in sedimentary rocks and

  1. Evaluation of metasomatic changes in an interlayered blueschist-greenschist sequence (Coastal Cordillera, Chile) by combining geochemical data with equilibrium assemblage diagrams (United States)

    Halama, Ralf; Konrad-Schmolke, Matthias


    In the Coastal Cordillera of Central Chile, a spectacular sequence of interlayered blueschists and greenschists occurs in coastal outcrops near Pichilemu. Three explanations are generally proposed to interpret the interlayering of metamorphic rocks that represent distinct metamorphic facies: 1. Differences in the pressure-temperature (P-T) conditions of equilibration and late-stage tectonic juxtaposition, 2. Chemical differences between the layers inherited from the protolith, and 3. Differences in the degree of metasomatic overprint during metamorphism. Investigations of such interlayered sequences can shed light on the mobility of elements and fluid-rock interaction during metamorphism. To identify the processes responsible for interlayering, geochemical analyses were combined with petrologic investigations involving the calculation of isothermal and isobaric binary phase diagrams using the THERIAK-DOMINO [1] software. Major mineral phases in blueschist and greenschist layers are amphibole, white mica, chlorite, and albite with subordinate amounts of titanite, epidote, hematite and apatite. The mineralogy of blueschist and greenschist layers is similar, albeit the modal proportions differ, causing the distinct colouring. Peak P-T conditions of blueschists reach 370±20 °C at 10±1 kbar [2]. The layering on a cm-to-dm scale and the similar mineralogy suggest that both blueschist and greenschist layers experienced a similar P-T evolution. For adjacent blueschist-greenschist pairs, blueschists have consistently higher Si and Na contents, whereas greenschists are relatively enriched in Al, Mg and total Fe. However, the observed major element geochemical trends are inconsistent with magmatic differentiation. For several blueschist-greenschist pairs, ratios of incompatible trace elements, which are indicative of the protolith composition and considered as relatively immobile during low-T metamorphism (Th/Yb, Nb/Yb), are near identical. These features point to

  2. Petrological cannibalism: the chemical and textural consequences of incremental magma body growth (United States)

    Cashman, Kathy; Blundy, Jon


    The textures of minerals in volcanic and plutonic rocks testify to a complexity of processes in their formation that is at odds with simple geochemical models of igneous differentiation. Zoning in plagioclase feldspar is a case in point. Very slow diffusion of the major components in plagioclase means that textural evidence for complex magmatic evolution is preserved, almost without modification. Consequently, plagioclase affords considerable insight into the processes by which magmas accumulate in the crust prior to their eventual eruption or solidification. Here, we use the example of the 1980-1986 eruptions of Mount St. Helens to explore the causes of textural complexity in plagioclase and associated trapped melt inclusions. Textures of individual crystals are consistent with multiple heating and cooling events; changes in total pressure ( P) or volatile pressure () are less easy to assess from textures alone. We show that by allying textural and chemical analyses of plagioclase and melt inclusions, including volatiles (H2O, CO2) and slow-diffusing trace elements (Sr, Ba), to published experimental studies of Mount St. Helens magmas, it is possible to disambiguate the roles of pressure and temperature to reconstruct magmatic evolutionary pathways through temperature-pressure-melt fraction ( T-- F) space. Our modeled crystals indicate that (1) crystallization starts at > 300 MPa, consistent with prior estimates from melt inclusion volatile contents, (2) crystal cores grow at = 200-280 MPa at F = 0.65-0.7, (3) crystals are transferred to = 100-130 MPa (often accompanied by 10-20 °C of heating), where they grow albitic rims of varying thicknesses, and (4) the last stage of crystallization occurs after minor heating at ~ 100 MPa to produce characteristic rim compositions of An50. We hypothesize that modeled decreases in excess of ~50 MPa most likely represent upward transport through the magmatic system. Small variations in modeled , in contrast, can be effected by

  3. Mesozoic metamorphism and its tectonic implication along the Solonker suture zone in central Inner Mongolia, China (United States)

    Zhang, Jinrui; Wei, Chunjing; Chu, Hang; Chen, Yaping


    The Xing'an-Inner Mongolia Orogenic Belt (XIMOB) exposed in the eastern section of the Central Asian Orogenic Belt (CAOB) is generally thought to have resulted from closure of the Paleo-Asian Ocean. However, disputations still exist on the age and detailed tectonic processes involved in its final amalgamation. The Solonker suture zone in the central Inner Mongolia, once recognized as the major paleo-plate boundary recording the terminal collision of the XIMOB, is characterized by extensive regional low-temperature metamorphism of greenschist to epidote-amphibolite facies with local presence of blueschists, which lacks systematic study. Four metabasite and garnet-mica schist samples were studied for determination of metamorphic P-T evolution using pseudosection and conventional thermobarometry. The two metabasite samples from Wulangou and Daqing Pasture contain actinolite, albite, epidote, chlorite and hornblende (in Daqing Pasture) and are estimated to have peak P-T conditions of 5.2-5.9 kbar/415-450 °C in Wulangou and 7.0-7.9 kbar/470-475 °C in Daqing Pasture. Two garnet-mica schist samples from Shuangjing (or Shuangjing schist) contain garnet porphyroblasts, muscovite, quartz, plagioclase, chlorite with or without potassium feldspar, biotite, and calcite, and are modeled to record prograde P-T vectors respectively of 3.0 kbar/482 °C-3.3 kbar/495 °C and 4.2 kbar/478 °C-4.8 kbar/483 °C, followed by near-isothermal decompression. The zircon U-Pb dating analyses suggest that the metamorphism probably occurred soon afterwards in the Early Mesozoic. The peak P-T conditions for the metabasite and garnet-mica schist samples yield thermal gradients respectively of 18-22 °C/km and 26-33 °C/km, being intermediate and low P/T series, and the metamorphic evolution in these rocks characteristic of clockwise P-T paths may correspond to tectonic thickening and thinning processes. The extensive low-temperature metamorphism of intermediate to low P/T types along the

  4. Los sistemas geotermales del Pirineo central. I. Caracteres geoquímicos y fisicoquímicos de los manantiales termales

    Directory of Open Access Journals (Sweden)

    Gómez, J.


    Full Text Available The compositional characters of selected hot springs from the Panticosa, Benasque, Arties, Caldas de Bohí, Luchon and Cauterets geothermal systems in the Central Pyrenees have been studied. All the springs have the same global geochemical features (high pH, low total dissolved solids, very low Mg concentrations, Na as the dominant cation, and absence of a dominant anion and belong to the same granite-related alkaline thermal waters group. Chemical composition of the springs is similar to each other, and to that found in other Pyrenean geothermal systems. A more detailed comparison shows, however, that Panticosa and Benasque systems have the lowest sodium and potassium concentrations found in any water belonging to the group of alkaline waters. Differences in pH values among the springs are related to emergence temperature as it occurs in the Pyrenean geothermal systems. According to the high pH of these waters, speciation calculations at emergence temperature show a very low CO2 partial pressure, dissolved silica partially ionized as H3Si04-, and Al(OH4- as the dominant aluminium species. Saturation indexes show that almost al1 the waters are highly oversaturated with quartz (close to equilibrium with chalcedony, potassium feldspar, and albite, which are the minerals equilibrated at depth with the solutions. Furthermore, all waters are in equilibrium with kaolinite and ca1cite at emergence conditions, showing the existence of a reequilibrium process during their ascent to the surface. This process happens to be one of the most important in the geochemical evo1ution of these alkaline systems.Las aguas de los sistemas geotermales de Panticosa, Benasque, Arties, Caldas de Bohí, Luchon y Cauterets en el Pirineo Central presentan rasgos geoquímicos similares (valores de pH elevados, bajo contenido de sólidos disueltos, muy bajas concentraciones de Mg, sodio como catión dominante y sin un anión en proporciones preponderantes sobre los dem

  5. Ore features and gold occurrence in Yinwagou Gold Deposit,Gansu Province%甘肃阴洼沟金矿床矿石特征及金的赋存状态研究

    Institute of Scientific and Technical Information of China (English)

    赵民; 郭月琴; 赵国斌; 温志亮; 杨鹏飞; 李普涛; 吴天娇


    Characteristics of gold minerals and the occurrence of gold have been determined in Yinwagou Gold Deposit ,on the basis of systematic laboratory study ,such as electron microscope observation ,multi-element analysis ,e-lectronic microprobe energy spectrum analysis , electronic microprobe wavelength spectrum analysis , mineral phase a-nalysis .The result shows the gold ores mainly have three different mineralogical types ,that is low sulphide altered rock type gold ore,low sulphide cataclastic quartz-vein type gold ore and low sulphide ankerite -albite-quartz-vein type gold ore ,and Au is the only one industrially valuable element;the metallic mineral content in the ore is low and they are mainly limonite ,hematite and pyrite;non-metallic minerals are mainly quartz ,followed by sericite ,carbonate min-erals,feldspar,chlorite and kaolinite; gold minerals are native gold,and the average fineness of native gold is 975;The main type of dissemination is fissure gold ,followed by inclusion gold ,few in the form of the intergranular gold;grain size of native gold is dominated by fine visible gold ,followed by microgranular gold .Native gold is primarily visi-ble gold,followed by microscopic gold .%为了查清阴洼沟金矿床矿石特征及金的赋存状态,采用电子显微镜、多元素分析、电子探针能谱分析、电子探针波谱分析、物相分析等技术方法,对阴洼沟金矿床的金矿石、金矿物进行了系统的研究.研究结果表明:金矿石工艺类型主要有少硫化物蚀变岩型金矿石、少硫化物碎裂石英脉型金矿石和少硫化物铁白云石-钠长石-石英脉型3种,且有工业价值的元素只有Au;矿石中金属矿物含量较低,主要是褐铁矿、赤铁矿及黄铁矿,非金属矿物主要是石英,其次是绢云母、碳酸盐矿物、长石、绿泥石及高岭石;金矿物为自然金,金成色平均为975;金的嵌布类型以裂隙金为主,其次为包裹金,粒间金含量较少;自然金以细

  6. Amphibole equilibria as monitors of P-T path and process in the exhumation of HP/UHP terranes (United States)

    Waters, David; Airaghi, Laura; Czertowicz, Thomas


    Recent advances in modelling and the development of refined activity-composition relations allow the calculation of phase diagrams involving complex mineral solid solutions, such as calcic, sodic-calcic and sodic amphiboles (e.g. Diener et al., 2007, J metamorphic Geol.). Amphiboles are commonly found in eclogite facies metabasites, and formed at different metamorphic stages. Such rocks commonly show complex reaction microstructures that reveal their history. The focus in this contribution is on two distinct amphibole types: coarse, post-peak matrix amphibole, and amphibole involved in symplectitic microstructures replacing omphacite. These studies serve as a test of the current activity models and calculation approaches, but more importantly as a framework for understanding the processes and P-T path during exhumation of subducted terranes. Examples are taken from the Western Gneiss Complex of Norway and from the Kaghan Valley (Pakistan), but are more generally applicable to crustal blocks that have exhumed through the P-T 'window' in which comparable petrological features develop. The microstructural types of interest here are: broad irregular interstitial amphibole grains, which commonly merge with a coarse spongy intergrowth of amphibole with quartz and/or albite (most likely replacing omphacite); and a fine-grained symplectite of low-Na clinopyroxene with sodic plagioclase and minor hornblende invading omphacite. Many specimens show these varieties as a sequence, inferred to reflect decreasing pressure (and ultimately, temperature). Amphibole compositions cover a wide range: the most sodic occur in large interstitial grains and fall near the junction of the winchite, barroisite and taramite fields of the IMA classification; they trend towards a pargasitic hornblende, still with significant glaucophane component; spongy amphiboles typically lie on a trend towards lower glaucophane component; symplectite amphibole is generally a common hornblende on a typical

  7. The plutonic-volcanic connection: are we even on the right track? (Invited) (United States)

    Lundstrom, C.; Chakraborty, P.; Zambardi, T.


    PV work reflecting vapor formation lead to a self sustaining chain reaction releasing all water-rich phase in the mush as it sweeps upward. In the uppermost mush, crystals dissolve into the water-rich phase producing an aphyric silicic eruptive product. We performed cold seal experiments to measure dissolution. We sealed hydrous peralkaline melt (25mg of either Na-K-Al-Si glass or Na2SiO3 + 25mg H2O) with single crystals of qtz, albite and k-spar in gold capsules at variable temperature. The melt dissolves >35mg of granite (qtz plus 2 feldspars) at 600°C and 1 kbar providing viability to the idea. Although speculative, this scenario avoids the problem of lacking latent heat to completely melt the mush but instead calls upon dissolution. This model has critical hazards implications since it suggests that calderas with no seismically visible blobs of melt could generate large eruptive volumes in relatively short timescales. 1) Mahood, EPSL 99, 1990; 2) Lundstrom GCA 73, 2009; 3) Huang et al. GCA 73, 2009; 4) Friedman and Tuttle, JACS 70, 919, 1948.

  8. 搭格架温泉水化学特征及其约束因素研究%Hydrochemical Characteristics and Constraints of Hot Springs in Dagejia Geothermal Field, Tibet, China

    Institute of Scientific and Technical Information of China (English)

    王香桂; 伍乾富; 伍坤宇; 沈立成


    搭格架地热区温泉水DJ1-DJ116号样品于2009年采集,阳离子及微量元素含量采用ICP-OES法测试,Cl(-)含量采用滴定法测试,其余阴离子含量采用紫外-可见光分光光度法测试.通过对温泉水化学指标的分析,研究温泉的水化学特征及约束因素.其温泉水化学类型为HCO(3)-Na型,平均矿化度为1524 mg/L,具有较高的Na/Cl值,温泉水演化程度较高,为完全平衡水,热储中的水岩反应达到了平衡状态.温泉水中PO(2)极低,PCO(2)较高;大部分温泉水中玉髓、石英和无定形态Si0(2)三种硅质热液矿物的饱和度指数大于0.K-Na温标计算热储平均平衡温度为251.36℃,泉水中的Na(+),K(+)离子活度主要受到钠、钾长石的约束.微量元素组合表现出花岗岩源的特征.总体上搭格架地热区温泉水化学特征受到区域地质背景的约束.%The hot water samples DJ1-DJ116 were collected in 2009.Cations and trace elements were analyzed by the ICP-OES method, Cl- content was tested by the titration method, and the other anions were tested by the UV-visible spectrometry method.Through analyzing the chemical indicators of hot springs we study the characteristics and constraints of the water.The hydrochamical type of the hot springs is HCO3-Na, the average salinity is 1 524 mg/L and Na/Cl value is high.The evolution level of the water is equilibrium water and water-rock reaction in thermal reservoir has reached equilibrium.The waters are with very low partial pressure of oxygen and higher partial pressure of dioxide carbon.The saturation index of three kinds of silica minerals in most water samples are >0.The average equilibrium temperature of thermal reservoir is 251.36℃, which is calculated by K-Na geo-thermometer.The activities of Na+, K+ are constrained by albite and K-feldspar minerals.The characteristics of trace elements portfolio show that they are originated in granite.Take the whole, the hydrochemical characteristics of the

  9. Evolution of fluid-rock interactions: fluid inclusion, isotopic, and major/minor element chemistry of hydrothermally altered volcanic rock in core RN-17B, Reykjanes, Iceland (United States)

    Fowler, A. P.; Zierenberg, R. A.; Schiffman, P.; Marks, N. E.; Fridleifsson, G. O.


    The Reykjanes Peninsula, Iceland, hosts a seawater-dominated geothermal system. Previous studies indicate an evolution of the system from meteoric to seawater. The inclined 4-inch diameter RN-17B drill core was collected from 2798.5 m to 2808.5 m (~2555 m below surface) at in situ temperature of approximately 330°C. Samples for this study were obtained from the Iceland Deep Drilling Project (IDDP). The core contains hydrothermally altered rocks of basaltic composition. Hydrothermal alteration ranges from upper greenschist to lower amphibolite grade, dependent on protolith size and composition. Veins in the core grade inward from radial epidote + acicular hornblende + titanite + pyrite, to clearer equant and compositionally zoned epidote vein centers. Felted amphibole replaces hyaloclastite and smaller crystalline clasts within the core, but is absent from the centers of crystalline pillow basalt fragments. Amphibole in vein selvages and vesicle fillings is green and acicular. Electron microprobe analyses of amphibole indicate it spans a compositional range of ferrohornblende through paragasite. The pistacite component (Xps) of vein epidote ranges from 16.5 to 36.7. The Xps component shows both normal and reverse zoning within single epidote crystals across this range, and follows no distinct pattern. Vein epidote adjacent to the wall rock has a higher aluminum concentration than vein centers. This may be due to mobilization of aluminum from plagioclase in the wall rock during albitization. Solutions flowing through open fractures may have lower Al-content and thus precipitate more Fe-rich epidote than those next to the fracture walls. Primary fluid inclusions in epidote range in size from <1 to 10 μm in diameter. Secondary fluid inclusions are <1 μm in diameter and not measurable. Calculated fluid inclusion salinities range from 0.5 to 7.6 weight percent NaCl, with lower salinities adjacent to the wall rock and higher salinities in the vein centers

  10. Mineral chemistry and magnetic petrology of the Archean Planalto Suite, Carajás Province - Amazonian Craton: Implications for the evolution of ferroan Archean granites (United States)

    Cunha, Ingrid Roberta Viana da; Dall'Agnol, Roberto; Feio, Gilmara Regina Lima


    The Planalto Suite is located in the Canaã dos Carajás subdomain of the Carajás Province in the southeastern part of the Amazonian Craton. The suite is of Neoarchean age (∼2.73 Ga), ferroan character, and A-type affinity. Magnetic petrology studies allowed for the distinction of two groups: (1) ilmenite granites showing low magnetic susceptibility (MS) values between 0.6247×10-3 and 0.0102 × 10-3 SI and (2) magnetite-ilmenite-bearing granites with comparatively higher but still moderate MS values between 15.700×10-3 and 0.8036 × 10-3 SI. Textural evidence indicates that amphibole, ilmenite, titanite, and, in the rocks of Group 2, magnetite also formed during magmatic crystallization. However, compositional zoning suggests that titanite was partially re-equilibrated by subsolidus processes. The amphibole varies from potassian-hastingsite to chloro-potassian-hastingsite and shows Fe/(Fe + Mg) > 0.8. Biotite also shows high Fe/(Fe + Mg) ratios and is classified as annite. Plagioclase porphyroclasts are oligoclase (An25-10), and the grains of the recrystallized matrix show a similar composition or are albitic (An9-2). The dominant Group 1 granites of the Planalto Suite were formed under reduced conditions below the FMQ buffer. The Group 2 granites crystallized under more oxidizing conditions on or slightly above the FMQ buffer. Pressures of 900-700 MPa for the origin and of 500-300 MPa for the emplacement were estimated for the Planalto magmas. Geothermometers suggest initial crystallization temperatures between 900 °C and 830 °C, and the water content in the magma is estimated to be higher than 4 wt%. The Neoarchean Planalto Suite and the Estrela Granite of the Carajás Province reveal strong mineralogical analogies, and their amphibole and biotite compositions have high total Al contents. The latter characteristic is also observed in the same minerals of the Neoarchean Matok Pluton of the Limpopo Belt but not in those of the Proterozoic rapakivi A

  11. Multiple deformation mechanisms operating at seismogenic depths: Tectonic pseudotachylyte and associated deformation from the central Sierra Nevada, California (United States)

    Prante, M. R.; Evans, J. P.


    pseudomorphs after biotite and alteration of mafic phases to epidote, sericite and calcite alteration of albite, and calcite and chlorite filled veins. Cross-cutting calcite veins contain fine-grained calcite with abundant twins up to 20 μm-thick. Multiple pseudotachylyte injection veins and reworked pseudotachylyte in cataclastic rock suggest multiple earthquakes along the GPF and GLF at depths favorable to pseudotachylyte formation. Abundant hydrothermal alteration and cross-cutting calcite veins with thick (> 1 μm) twins is consistent with ambient temperatures between 170 and 200°C. These temperatures are generally consistent with the reported ambient temperature conditions during pseudotachylyte formation. Crystal-plastic deformation of quartz and feldspar in the GPF and GLF zones is consistent with deformation at temperatures between 200-400°C. Frictional melt and associated brittle and plastic deformation, and fluid alteration are presumed to have occurred at similar temperature conditions and may be coeval. These results have important implication for understanding energy sinks associated with seismic slip and the conditions of tectonic pseudotachylyte formation.

  12. Mineralogy and chemistry of the green stone artifacts (muiraquitãs of the museums of the Brazilian State of Pará Mineralogia e química de artefatos de pedra verde (muiraquitãs dos Museus do Estado do Pará

    Directory of Open Access Journals (Sweden)

    Anna Cristina Resque Meirelles


    Full Text Available Muiraquitãs, lithic artifacts found in the Amazon basin, have been considered to be Asian in origin, or to have been sculpted by the legendary female Amazon warriors. These pieces are now very rare, and are found mainly in museum collections. In the present study, the mineralogical and chemical content of 23 specimens from the collections of the Museu de Gemas (Gemstone Museum and Museu do Encontro (Meeting Museum in Belém, Brazil, were analyzed. Most of the pieces were made of minerals commonly found in Brazil - quartz, albite, microcline, variscite, anorthite, and tremolite (the equivalent of nephritic jade. However, four of the pieces were made of jadeite, that is, jadeitic jade, which is unknown in the Amazon basin or in other parts of Brazil. The confirmation of the presence of this mineral in some of the artifacts reopens the debate on the mineralogical origin of the muiraquitãs found in the Amazon basin. Before the present discovery, their origin was defended as Amazonian due to the absence of jadeite jade in the searched pieces and the fact that jadeite was not found in Brazil but in Central America and Asia.Os muiraquitãs foram considerados de proveniência asiática ou, também, como peças esculpidas pelas lendárias mulheres guerreiras, as Amazonas. São peças, hoje, muito raras, encontradas em alguns acervos de Museus. Estudos mineralógicos e químicos de 23 peças do acervo dos Museus de Gemas e do Encontro em Belém, Brasil, mostraram que os muiraquitãs podem ser constituídos, tanto de quartzo, como de albita, ou microclínio, pirofilita, variscita, anortita e tremolita (equivalente ao jade nefrítico, minerais frequentes em formações geológicas do Brasil. No entanto quatro peças são constituídas de jadeíta, ou seja, em jade jadeítico, raro e desconhecido na Amazônia e Brasil. A constatação da presença desse mineral reacende a discussão em torno da origem mineralógica dos muiraquitãs encontrados na Amaz

  13. Rheology linked with phase changes as recorded by development of shear bands in the South Armorican Shear Zone (United States)

    Jeřábek, Petr; Bukovská, Zita


    The South Armorican Shear Zone in France represents a major right-lateral strike slip shear zone formed in the late stages of Variscan orogeny. The active deformation in this shear zone is associated with the development of S-C fabrics in granitoids where thin shear bands (C) overprint an earlier higher grade metamorphic foliation (S). In the studied samples covering low to high intensity of shear band overprint, we identified three stages of shear band evolution associated with distinct microstructures and deformation mechanisms. The initiation of shear bands stage I is associated with the formation of microcracks crosscutting the S fabric and detected namely in the recrystallized quartz aggregates. The microcracks of suitable orientation are filled by microcline, albite, muscovite and chlorite which is a typical assemblage also for the well developed shear bands. Phase equilibrium modeling in PERPLEX indicates that this assemblage formed at pressure-temperature range of 0.1-0.4 GPa and 300-340 °C. Stage II of shear band evolution is characterized by dynamic recrystallization and grain size reduction of quartz aggregates along the microcracks and replacement of quartz by microcline along grain boundaries. This process leads to disintegration of quartz aggregate fabric and phase mixing in the shear bands. The inferred deformation mechanism for this stage is solution-precipitation creep although recrystallization of quartz is still active at the contact between quartz aggregates and shear bands. The coarse grained microstructure of quartz aggregates with ca ~250 microns average grain size reduces to ~10 microns grain size when recrystallized along extremely thin shear bands/microcracks and to ~20 microns grain size when recrystallized along the thicker shear bands. By using the flow law of Patterson and Luan (1990) for dislocation creep in quartz and the quartz piezometer of Stipp and Tullis (2003) corrected after Holyoke and Kronenberg (2010), the quartz

  14. Spatial and temporal zoning of hydrothermal alteration and mineralization in the Sossego iron oxide-copper-gold deposit, Carajás Mineral Province, Brazil: Paragenesis and stable isotope constraints (United States)

    Monteiro, Lena V.S.; Xavier, R.P.; Carvalho, E.R.; Hitzman, M.W.; Johnson, C.A.; Souza, Filho C.R.; Torresi, I.


    The Sossego iron oxide–copper–gold deposit (245 Mt @ 1.1% Cu, 0.28 g/t Au) in the Carajás Mineral Province of Brazil consists of two major groups of orebodies (Pista–Sequeirinho–Baiano and Sossego–Curral) with distinct alteration assemblages that are separated from each other by a major high angle fault. The deposit is located along a regional WNW–ESE-striking shear zone that defines the contact between metavolcano–sedimentary units of the ∼2.76 Ga Itacaiúnas Supergroup and tonalitic to trondhjemitic gneisses and migmatites of the ∼2.8 Ga Xingu Complex. The deposit is hosted by granite, granophyric granite, gabbro, and felsic metavolcanic rocks. The Pista–Sequeirinho–Baiano orebodies have undergone regional sodic (albite–hematite) alteration and later sodic–calcic (actinolite-rich) alteration associated with the formation of massive magnetite–(apatite) bodies. Both these alteration assemblages display ductile to ductile–brittle fabrics. They are cut by spatially restricted zones of potassic (biotite and potassium feldspar) alteration that grades outward to chlorite-rich assemblages. The Sossego–Curral orebodies contain weakly developed early albitic alteration and very poorly developed subsequent calcic–sodic alteration. These orebodies contain well-developed potassic alteration assemblages that were formed during brittle deformation that resulted in the formation of breccia bodies. Breccia matrix commonly displays coarse mineral infill suggestive of growth into open space. Sulfides in both groups of deposits were precipitated first with potassic alteration and more importantly with a later assemblage of calcite–quartz–epidote–chlorite. In the Sequeirinho orebodies, sulfides range from undeformed to deformed; sulfides in the Sossego–Curral orebodies are undeformed. Very late, weakly mineralized hydrolytic alteration is present in the Sossego/Currral orebodies. The sulfide assemblage is dominated by chalcopyrite with

  15. Los sistemas geotermales del Pirineo Central. II. Resultados de la aplicación de técnicas geotermométricas

    Directory of Open Access Journals (Sweden)

    Gimeno, M. J.


    Full Text Available Reservoir temperatures are calculated for six geothermal systems in the Central Pyrenees (Arties, Caldas de Bohí, Benasque, Panticosa, Luchon and Cauterets using different geothermometrical methods. In general, the selected hot springs have similar geochemical features belonging to the group of alkaline thermal systems installed in granitic environments. More in detail, however, it is important to note that Na and K concentrations of Panticosa and Benasque thermal springs are the lowest found in this water group to date. Both classical geothermometers and modeling calculations agree within a few degrees for the Arties, Caldas and Luchon geothermal systems: thermal waters are in equilibrium in their reservoirs with a common mineral association (quartz, albite, K-feldspar, caolinite and some calc-aluminum silicate at 103, 107 and 127° C, respectively. Cauterets, Panticosa and Benasque thermal waters appear to be equilibrated with the same mineral association at 98, 107 and 94° C, respectively as deduced from silica and Na-K geothermometers. Na-K-Ca and Ca-K geothermometers provide lower temperatures for these systems, probably because of some exchange of calcium between rock and water during the ascent of solutions. Nevertheless, the modeling calculations fail to represent the composition of Panticosa and Benasque thermal springs: these waters are out of equilibrium with the selected mineral association at the temperatures given by Na-K and SiO2-quartz geothermometers Therefore, the agreement between these geothermometers appear to be fortuitous, specially for Benasque thermal waters.Mediante la utilización de distintas técnicas geotermométricas se han estimado las temperaturas en el reservorio de seis sistemas geotermales (Arties, Caldas de Bohí, Benasque, Panticosa, Luchon y Cauterets instalados en los materiales graníticos del Pirineo Central. Los manantiales seleccionados para realizar los cálculos muestran similares caracteres

  16. Micro-structural and compositional variations of hydrothermal epidote-group minerals from a peralkaline granite, Corupá Pluton, Graciosa Province, South Brazil, and their petrological implications

    Directory of Open Access Journals (Sweden)

    Silvio R.F. Vlach


    Full Text Available Epidote-group minerals, together with albite, quartz, fluorite, Al-poor and Fe-rich phyllosilicates, zircon, and minor oxides and sulphides, are typical hydrothermal phases in peralkaline alkali-feldspar granites from the Corupá Pluton, Graciosa Province, South Brazil. The epidote-group minerals occur as single crystals and as aggregates filling in rock interstices and miarolitic cavities. They display complex recurrent zoning patterns with an internal zone of ferriallanite-(Ce, followed by allanite-(Ce, then epidote-ferriepidote, and an external zone with allanite-(Ce, with sharp limits, as shown in BSE and X-ray images. REE patterns show decreasing fractionation degrees of LREE over HREE from ferriallanite to epidote. The most external allanite is enriched in MREE. LA-ICP-MS data indicate that ferriallanite is enriched (>10-fold in Ti, Sr and Ga, and depleted in Mg, Rb, Th and Zr relative to the host granite. Allanite has lower Ga and Mn and higher Zr, Nb and U contents as compared to ferriallanite, while epidote is enriched in Sr, U and depleted in Pb, Zr, Hf, Ti and Ga. The formation of these minerals is related to the variable concentrations of HFSE, Ca, Al, Fe and F in fluids remaining from magmatic crystallization, in an oxidizing environment, close to the HM buffer. L-MREE were in part released by the alteration of chevkinite, their main primary repository in the host rocks.Minerais do grupo do epidoto, com albita, quartzo, fluorita, filossilicatos pobres em Al e ricos em Fe, zircão e quantidades menores de óxidos e sulfetos são fases hidrotermais típicas em álcali-feldpato granitos peralcalinos do Pluton Corupá, Província Graciosa, Sul do Brasil. Os minerais do grupo do epidoto ocorrem como cristais individuais ou agregados que preenchem interstícios e cavidades miarolíticas na rocha. Mostram zonamento complexo, recorrente, descrito por uma zona interna de ferriallanita-(Ce, seguida por allanita-(Ce, epidoto-ferriepidoto e uma

  17. Petrogénesis del plutón monzogranítico peralumínico de Santa Eufemia (Batolito de los Pedroches, Córdoba

    Directory of Open Access Journals (Sweden)

    Fenoll Hach-Alí, P.


    Full Text Available The Santa Eufemia pluton is part of the composite magmatic assoclatlon of Los Pedroches batholith, located in the southern branch of the Central Iberian Zone of the Hercynian orogenic belt of Spain. This high-Ievel postkynematic batholith consists of three main types of plutonic rocks: boitite±amphibole granodiorites, biotite-cordierite porphiritic monzogranites and cordierite leucogranites. The Santa Eufemia pluton consists of biotite-cordierite monzogranites, and in a lesser extent of cordierite leucogranites. Scarce enclaves of different type are found in the monzogranites, biotiteplagioclase- eordierite and fine grained porphiritic monzogranite enclaves being the most common. The petrographic, structural and geochemical (major and trace elements data suggests a compiex evolutionary history of a metasedimentary-source monzogranitic magma with no genetical relationships with more basic magmas such as the one which is now represented by the granodiorite facies of the batholith. Non-minimum melt and reequilibrated source material (secondary restites mixing during the ortomagmatic evolution of the magma accounts for the compositional heterogenities of the monzogranites. The ultimate product of this evolution is the segregation of a fluid-saturated residual liquid in the final level of intrusion of the magma, leading to the emplacement of leucogranite masses and dikes and the exsolution of a supercritical fluid phase related with the late magmatic recrystallization of sorne mineral phases (muscovite, albite, quartz, tourmaline, topaz, the geochemical removilization of sorne incompatible trace elements (Rb, Cs, Li, Be, Sn, Nb due to fluid-rock interactions and the formation of periplutonic wolframite-arsenopyritequartz mineralizations.El plutón de Santa Eufemia forma parte del batolito de Los Pedroches, situado en el extremo sudoccidental de la Zona Centro-Ibérica del Macizo Hercínico español. Este batolito de carácter epizonal y postcinem

  18. Geochronology and geochemistry of gneissic metagranites in eastern Dabie Mountains:Implications for the Neoproterozoic tectono-magmatism along the northeastern margin of the Yangtze Block

    Institute of Scientific and Technical Information of China (English)


    The gneissic metagranites with Neoproterozoic protolith ages are widely exposed along the eastern margin of the Dabie ultra-high-pressure(UHP) metamorphic belt.In this paper,five representative plutons,including Huangzhen,Daba,Shima,Shuanghe,and Sanzusi,were selected for a detailed chronological and geochemical study aiming to identify the nature of the protoliths and to reveal their implications for the Neoproterozoic tectono-magmatic evolution along the northeastern margin of the Yangtze Block.These gneissic metagranites consist mainly of quartz,albite(oligoclase) and K-feldspar,and minor amphibole and biotite,as well as some metamorphic minerals due to the UHP metamorphism,such as phengite,epidote and minor kyanite and garnet.Mafic alkaline minerals(e.g.,aegirine or aegirine-augite) have been observed in some of these plutons.Zircon LA-ICP-MS U-Pb dating results indicate that the protoliths of the gneissic metagranites have been generated in Mid-Neoproterozoic(770-780 Ma),and suffered both ultrahigh-pressure metamorphism in Early Mesozoic and subsequently high-pressure eclogite-facies recrystallization at about 215 Ma.Although the gneissic metagranites generally have high SiO2 contents(70.23%-77.23%) and show metaluminous-weakly peraluminous signatures(ASI=0.90-1.05),there are still some geochemical variances between different plutons.Compared with the Sanzusi pluton,the metagranites from the Huangzhen,Daba,Shima,and Shuanghe have high K2O+Na2O contents(7.76%-9.45%),FeOtotal/(FeOtotal+MgO) ratios(0.82-0.96),HFSEs and Ga concentrations with an average 104×Ga/Al ratio up to 3.07.Combined with the features that the four plutons commonly contain aegirine-augite and have high zircon saturation temperatures(816-918°C),it is suggested that their proto-liths belong to peralkaline A-type granites.The Sanzusi pluton generally contains biotite and epidote generated from metamorphic reaction of amphibole,and is chemically enriched in calcium and depleted in potassium with

  19. Mass transfer and fluid evolution in late-metamorphic veins, Rhenish Massif (Germany): insight from alteration geochemistry and fluid-mineral equilibria modeling (United States)

    Marsala, Achille; Wagner, Thomas


    Element mobility and fluid-rock interaction related to the formation of late-metamorphic quartz veins have been studied by combination of mineral chemistry, whole-rock geochemistry, mass balance analysis and fluid-mineral equilibria modeling. The quartz veins are hosted by very low-grade metasedimentary rocks of the fold-and-thrust belt of the Rhenish Massif (Germany). The veins record two stages of evolution, a massive vein filling assemblage with elongate-blocky quartz, chlorite, apatite and albite, and a later open space filling assemblage with euhedral crystals of quartz, ankerite-dolomite and minor calcite and sulfides. Detailed mass balance analysis of an alteration profile adjacent to a representative quartz vein demonstrates that element mobility is restricted to the proximal zone. The most important element changes are gain of Ca, Fe, Mg, Mn, P and CO2, and loss of Si, K and Na. The data demonstrate that wall-rock carbonation is one of the main alteration features, whereas mobility of Si, K and Na are related to dissolution of quartz and destruction of detrital feldspar and muscovite. The whole-rock geochemical data, in conjunction with fluid composition data and pressure-temperature estimates, were used as input for fluid-mineral equilibria modeling in the system Si-Al-Fe-Mg-Ca-Na-K-C-S-O-H-B-F-Cl. Modeling involved calculation of rock-buffered fluid compositions over the temperature interval 100-500 °C, and reaction-path simulations where a rock-buffered high-temperature fluid reacts with fresh host-rocks at temperatures of 400, 300 and 200 °C. Calculated rock-buffered fluid compositions demonstrate that retrograde silica solubility is a strong driving force for quartz leaching in the temperature-pressure window of 380-450 °C and 0.5 kbar. These conditions overlap with the estimated temperatures for the initial stage of vein formation. Reaction-path models show that high-temperature alteration can produce the observed silica leaching, suggesting that

  20. The geology of the Morro Velho gold deposit in the Archean Rio das Velhas greenstone belt, Quadrilátero Ferrífero, Brazil (United States)

    Vial, Diogenes Scipioni; DeWitt, Ed; Lobato, Lydia Maria; Thorman, Charles H.


    The Morro Velho gold deposit, Quadrilátero Ferrífero region, Minas Gerais, Brazil, is hosted by rocks at the base of the Archean Rio das Velhas greenstone belt. The deposit occurs within a thick carbonaceous phyllite package, containing intercalations of felsic and intermediate volcaniclastic rocks and dolomites. Considering the temporal and spatial association of the deposit with the Rio das Velhas orogeny, and location in close proximity to a major NNW-trending fault zone, it can be classified as an orogenic gold deposit. Hydrothermal activity was characterized by intense enrichment in alteration zones of carbonates, sulfides, chlorite, white mica±biotite, albite and quartz, as described in other Archean lode-type gold ores. Two types of ore occur in the deposit: dark gray quartz veins and sulfide-rich gold orebodies. The sulfide-rich orebodies range from disseminated concentrations of sulfide minerals to massive sulfide bodies. The sulfide assemblage comprises (by volume), on average, 74% pyrrhotite, 17% arsenopyrite, 8% pyrite and 1% chalcopyrite. The orebodies have a long axis parallel to the local stretching lineation, with continuity down the plunge of fold axis for at least 4.8 km. The group of rocks hosting the Morro Velho gold mineralization is locally referred to as lapa seca. These were isoclinally folded and metamorphosed prior to gold mineralization. The lapa seca and the orebodies it hosts are distributed in five main tight folds related to F1 (the best examples are the X, Main and South orebodies, in level 25), which are disrupted by NE- to E-striking shear zones. Textural features indicate that the sulfide mineralization postdated regional peak metamorphism, and that the massive sulfide ore has subsequently been neither metamorphosed nor deformed. Lead isotope ratios indicate a model age of 2.82 ± 0.05 Ga for both sulfide and gold mineralization. The lapa seca are interpreted as the results of a pre-gold alteration process and may be

  1. Palaeomagnetic, rock-magnetic and mineralogical investigations of metadolerites from Western Svalbard : A preliminary report (United States)

    Michalski, Krzysztof; Nejbert, Krzysztof; Domańska-Siuda, Justyna; Manby, Geoffrey


    A group of 42 independently oriented palaeomagnetic samples from 7 sites located in central part of the West Spitsbergen Thrust and Fault Belt has been investigated. The samples were collected from 5 distinct metadolerite sheets intruded into the Proterozoic - Lower Paleozoic metamorphic complex of Western Oscar II Land (Western Svalbard Caledonian Terrane - Harland, 1997 division). All analyzed metadolerite samples were metamorphosed under greenschist facies metamorphism. The metamorphic assemblage consist of hornblende, biotite, actinolite, chlorite, epidote, stilpnomelane, titanite, albite, and quartz. Calcite, associated with pyrrhotite, pyrite chalcopyrite, sphalerite, and covellite, that occurs as irregular intergrowths or thin veins, document high activity of H2O-CO2-rich fluids during metamorphism. Primary magmatic phases represented by clinopyroxene occur rarely, and only in thick metadolerite dykes. Accessory oxides change their mineralogical and chemical composition during metamorphism. In all examined samples primary Ti-magnetite and oxy-exsolved hematite break-down completely into titanite or have been dissolved. The ilmenite are also replaced by titanite, but in metadolerites at contact with host metapelites, slightly altered ilmenite grains with preserved hematite exsolution were documented. Basing on mineralogical observations it should be expected that metamorphic processes have almost completely reset the paleomagnetic data record from the time of dolerite crystallization. This stage can document only rare hematite oxy-exsolution preserved within ilmenite, and presumably small inclusion of magnetite still preserved within unaltered clinopyroxene. The paleomagnetic record of metamorphic stage is probably recorded by pyrrhotite, hematite, goethite, and late Ti-free magnetite that can grow during breakdown of pyrrhotite to pyrite (Ramdohr. 1980). The NRM (Natural Remanent Magnetisation) intensities of the palaeomagnetic samples exceed the minimum 10

  2. Effect of MnO2 on the Microstructure and Properties of Phosphorous Slag Glass-ceramic%MnO2对磷渣微晶玻璃显微结构和性能的影响

    Institute of Scientific and Technical Information of China (English)

    汤李缨; 韩荣荟; 全健


    Sintering CaO-Al2O3-SiO2 glass-ceramic has compact and uniform structure, impact resistance, wear resistance, corrosion resistance, no radiation, rich color, beautiful texture features. It's a new environmental-friendly decorative material. In this paper, phosphorus slag was used as the main raw material, Fe2O3 and MnO2 as a coloring agent for preparation of beige glass-ceramics. X-ray diffraction, scanning electron microscope and other tests were used to investigate how MnO2 affected on the glass-ceramic microstructure, crystal phase types; the chemical durability of glass-ceramics was analyzed. The results showed that When MnO2 less than 5. 5%, the main phase was not changed, but crystallization was reduced, the size of crystals decreased from 0. 42 μm to 0. 3 μm; when MnO2 was 6%, the main phase became albite, the crystallization and the size of crystals all were increased. When MnO2 was more than 4%, each increased of 0. 5% MnO2 lower the flattening temperature about 10 ℃ , appropriate content of MnO2 improved the chemical durability.%烧结法CaO-Al2O3-SiO2微晶玻璃具有结构致密均匀,抗冲击、耐磨、耐腐蚀、无放射性、色泽丰富、纹理美观等特性,是一种新型绿色环保型装饰材料.以磷渣为主要原料,以Fe2Os和MnO2为着色剂,制备了米黄色微晶玻璃.利用X射线衍射和扫描电子显微镜等测试技术,研究了不同MnO2含量对微晶玻璃显微结构、晶相种类的影响,测定了微晶玻璃的化学稳定性.研究结果表明:当MnO2质量含量小于5.5%时,微晶玻璃主晶相为β-硅灰石,随着MnO2含量的增加析晶量减少,晶粒尺寸由0.42 μm减小到0.3 μm;当Mn02质量分数为6%时,主晶相变为钠长石且析晶量增加、晶体尺寸增大.当MnO2质量分数大于4%时,MnO2质量分数每增加0.5%其摊平温度约降低10℃,适量加入MnO2使其化学稳定性提高.

  3. Ultra Sodic gedrite and micro-scale metasomatic processes in granulitised kyanite eclogites from the Rhodope UHPM Province, Greece (United States)

    Moulas, Evangelos; Kostopoulos, Dimitrios K.; Connolly, James A. D.; Burg, Jean-Pierre


    The Rhodope Massif occupies most of northeastern Greece and southern Bulgaria and comprises high-grade metamorphic rocks such as metapelites with microdiamond inclusions. The (U)HP mineral paragenesis underwent extensive metamorphic overprint at granulite-facies followed by amphibolite-facies retrograde metamorphism. A kyanite-eclogite that occurs as lenses in orthogneisses from Thermes village was used to unravel the pressure-temperature-time path of the (U)HP rocks from the Rhodope. The peak-pressure mineral assemblage is omphacite, garnet, kyanite, phengite, rutile, apatite and zircon. Quartz is absent from the matrix and it can be found either as inclusions in garnet or as post-peak veins. This late quartz contains primary and secondary fluid inclusions implying the presence of a fluid phase during post high-pressure metamorphism. Kyanite is never observed in direct contact with quartz being armoured by an intervening stripe of plagioclase which itself shows zoning, becoming increasingly albitic towards quartz. Plagioclase formation at the Ky-Qtz interface requires certain Na and Ca influx that was provided by matrix omphacite. Two types of symplectites were formed by reaction between omphacite and kyanite. Firstly, corundum+plagioclase symplectites were formed at the expense of the jadeitic component of omphacite during decompression. Subsequently, the residual diopsidic component of omphacite reacted with the already formed corundum to give rise to spinel+plagioclase symplectites. The previous mechanisms demonstrate metasomatism in the micro-scale by diffusion controlled processes. During decompression matrix omphacite was decomposed to amphibole+plagioclase symplectites which reacted with garnet to form coronas consisting of two amphiboles (ortho- and clino-), plagioclase, ilmenite and magnetite. Biotite and plagioclase are also found as symplectites replacing phengite during decompression. Thermodynamic modelling of the symplectitic domains that replace

  4. Fe2O3对污泥与底泥制备轻质陶粒性能的影响%Effect of Fe2O3 on the characteristics of lightweight aggregate made from sewage sludge and river sediment

    Institute of Scientific and Technical Information of China (English)

    刘明伟; 许国仁; 李圭白


    The aim of this article is to investigate the effect of Fe2O3 contents on the characteristics of lightweight aggregate that is made from sewage sludge and river sediment.The physical characteristics,compressive strength,morphological structures and crystalline phases of lightweight aggregate were studied,and the results showed that the lightweight aggregate with higher bulk density,higher apparent density,and lower water absorption could be obtained at Fe2O3 contents between 3.5%-7%.The SEM analysis points out that the surface of lightweight aggregate exhibits more vitrification phenomenon as the Fe2O3 contents increase,the dense surface of lightweight aggregate with evenly distributed micro porous can be found at Fe2O3 contents=5%.The lightweight aggregate with stronger compressive strength(more than 14 MPa) can be obtained when Fe2O3 contents are between 3.5%-7%.The XRD analysis implies that the main crystal phase in the lightweight aggregate are quartz,albite-anorthite,kyanite and hematite,and the silicate crystals with stable structure are the main crystal in the internal of lightweight aggregate.As the Fe2O3 contents increase,more Fe2O3 will transform to hematite with crystal structure.The results indicate that the Fe2O3 contents between 3.5%-7% are appropriate in the process of making lightweight aggregate from sewage sludge and river sediment.%为研究在以污水污泥和河道底泥为主要原料制取轻质陶粒过程中,Fe2O3质量分数对陶粒性能的影响,对陶粒的物理性能、表面形态、抗压强度和晶体构成进行研究,结果表明,Fe2O3质量分数在3.5%~7%时,可取得松散容重和表观密度较高、吸水率比较小、抗压强度较高的陶粒.扫描电子显微镜(SEM)分析表明,随着Fe2O3质量分数的增加,陶粒表面玻璃化效果明显.在Fe2O3质量分数为5%时,可得到致密性较好、表面微孔分布均匀的陶粒.Fe2O3质量分数在3.5%~7%时,陶粒的抗压性能良好(14 MPa以上

  5. NMR and NQR studies of quadrupolar effects in glasses and polycrystals with half-integer spins (United States)

    Orengo-Aviles, Moises

    NMR and NQR and yielded Qsb{cc} = 1.89 MHz for sp{23}Na and eta=0.9. Furthermore the response from sp{23}Na in the polycrystalline forms of sodium molybdate, sodium tungstate, sodium stanate and albite was examined by means of NASP, pulsed NMR, and NQR. The sp{23}Na spectra for these compounds yielded values of Qsb{cc}, in the range 2.56 MHz to 2.80 MHz. A computer simulation program was used to simulate the spectra of sp{93}Nb-containing compounds. The survey of the niobium response in various polycrystalline compounds using the pulse-echo technique revealed first-order and second-order quadrupolar effects. The sp{93}Nb responses from five glasses in the Nbsb2Osb5-Nasb2O-SiOsb2 ternary glass system produced a second-order quadrupole pattern, but the response might contain more than one Nb site.

  6. The role of reaction affinity and secondary minerals in regulating chemical weathering rates at the Santa Cruz Soil Chronosequence, California (United States)

    Maher, K.; Steefel, Carl; White, A.F.; Stonestrom, D.A.


    In order to explore the reasons for the apparent discrepancy between laboratory and field weathering rates and to determine the extent to which weathering rates are controlled by the approach to thermodynamic equilibrium, secondary mineral precipitation, and flow rates, a multicomponent reactive transport model (CrunchFlow) was used to interpret soil profile development and mineral precipitation and dissolution rates at the 226 ka Marine Terrace Chronosequence near Santa Cruz, CA. Aqueous compositions, fluid chemistry, transport, and mineral abundances are well characterized [White A. F., Schulz M. S., Vivit D. V., Blum A., Stonestrom D. A. and Anderson S. P. (2008) Chemical weathering of a Marine Terrace Chronosequence, Santa Cruz, California. I: interpreting the long-term controls on chemical weathering based on spatial and temporal element and mineral distributions. Geochim. Cosmochim. Acta 72 (1), 36-68] and were used to constrain the reaction rates for the weathering and precipitating minerals in the reactive transport modeling. When primary mineral weathering rates are calculated with either of two experimentally determined rate constants, the nonlinear, parallel rate law formulation of Hellmann and Tisserand [Hellmann R. and Tisserand D. (2006) Dissolution kinetics as a function of the Gibbs free energy of reaction: An experimental study based on albite feldspar. Geochim. Cosmochim. Acta 70 (2), 364-383] or the aluminum inhibition model proposed by Oelkers et al. [Oelkers E. H., Schott J. and Devidal J. L. (1994) The effect of aluminum, pH, and chemical affinity on the rates of aluminosilicate dissolution reactions. Geochim. Cosmochim. Acta 58 (9), 2011-2024], modeling results are consistent with field-scale observations when independently constrained clay precipitation rates are accounted for. Experimental and field rates, therefore, can be reconciled at the Santa Cruz site. Additionally, observed maximum clay abundances in the argillic horizons occur at

  7. Fractional Crystallisation of Archaean Trondhjemite Magma at 12-7 Kbar: Constraints on Rheology of Archaean Continental Crust (United States)

    Sarkar, Saheli; Saha, Lopamudra; Satyanarayan, Manavalan; Pati, Jayanta


    fractionating from the magma are mostly clinopyroxene with minor orthopyroxene. Plagioclase crystals appear at pressures ≤ 15 kbar. Plagioclase crystals are mostly albitic in composition (XAb ~0.70-0.75). At each pressure, with progressive cooling and fractionation of solid phases, crystal-melt ratio becomes significantly higher, magma becomes more depleted in Al2O3, MgO, with significant increase in K2O/Na2O ratio and water content. With progressive cooling and fractionation, overall composition of the magma changes from trondhjemitic to granitic, with increase in viscosity from 4.5 poise to 5.5 poise. The study thus reveals that fractional crystallization of trondhemitic magmas at different depths can form more potassic granitic magma with higher viscosity. As Hf isotope signatures from most Archaean TTGs reveal longer crustal residence, it is likely that granitic magmas that became more common in the Neoarchaean period, could also possibly been derived by fractional crystallization from trondhjemitic magmas in Mesoarchaean time. Granitic magmas hence generated have much higher viscosity compared to the parent trondhjemitic magma. Low viscosity of trondhjemitic magmas and low crystal-melt ratios in the initial stages of crystallization (as derived in this study), may be the cause of formation of large bodies of TTGs in Early Archaean period. Close to Neoarchaean period more granitic magmas are observed. In this study it has been observed that crystallization of these magmas lead to high crystal-melt ratios and the magmas have higher viscosity. Such change in composition from Early to Neoarchaean time must have made Archaean crusts stronger and hence more prone to deformation. This observation hence support occurrence of Phanerozoic style signatures from poly-deformed terrains of Neoarchaean time.

  8. Rapid sedimentation of iron oxyhydroxides in an active hydrothermal shallow semi-enclosed bay at Satsuma Iwo-Jima Island, Kagoshima, Japan (United States)

    Kiyokawa, Shoichi; Ueshiba, Takuya


    Hydrothermal activity is common in the fishing port of Nagahama Bay, a small semi-enclosed bay located on the southwest coast of Satsuma Iwo-Jima Island (38 km south of Kyushu Island, Japan). The bay contains red-brown iron oxyhydroxides and thick deposits of sediment. In this work, the high concentration and sedimentation rates of oxyhydroxide in this bay were studied and the sedimentary history was reconstructed. Since dredging work in 1998, a thickness of 1.0-1.5 m of iron oxyhydroxide-rich sediments has accumulated on the floor of the bay. To estimate the volume of iron oxyhydroxide sediments and the amount discharged from hydrothermal vents, sediment traps were operated for several years and 13 sedimentary core samples were collected to reconstruct the 10-year sedimentary history of Nagahama Bay. To confirm the timing of sedimentary events, the core data were compared with meteorological records obtained on the island, and the ages of characteristic key beds were thus identified. The sedimentation rate of iron oxyhydroxide mud was calculated, after correcting for sediment input from other sources. The sediments in the 13 cores from Nagahama Bay consist mainly of iron oxyhydroxide mud, three thick tephra beds, and a topmost thick sandy mud bed. Heavy rainfall events in 2000, 2001, 2002, and 2004-2005 coincide with tephra beds, which were reworked from Iwo-Dake ash deposits to form tephra-rich sediment. Strong typhoon events with gigantic waves transported outer-ocean-floor sediments and supplied quartz, cristobalite, tridymite, and albite sands to Nagahama Bay. These materials were redeposited together with bay sediments as the sandy mud bed. Based on the results from the sediment traps and cores, it is estimated that the iron oxyhydroxide mud accumulated in the bay at the relatively rapid rate of 33.3 cm/year (from traps) and 2.8-4.9 cm/year (from cores). The pore water contents within the sediment trap and core sediments are 73%-82% and 47%-67%, respectively

  9. Influence of liquid structure on diffusive isotope separation in molten silicates and aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Watkins, J.M.; DePaolo, D.J.; Ryerson, F.J.; Peterson, B.


    Molecular diffusion in natural volcanic liquids discriminates between isotopes of major ions (e.g., Fe, Mg, Ca, and Li). Although isotope separation by diffusion is expected on theoretical grounds, the dependence on mass is highly variable for different elements and in different media. Silicate liquid diffusion experiments using simple liquid compositions were carried out to further probe the compositional dependence of diffusive isotopic discrimination and its relationship to liquid structure. Two diffusion couples consisting of the mineral constituents anorthite (CaAl{sub 2}Si{sub 2}O{sub 8}; denoted AN), albite (NaAlSi{sub 3}O{sub 8}; denoted AB), and diopside (CaMgSi{sub 2}O{sub 6}; denoted DI) were held at 1450°C for 2 h and then quenched to ambient pressure and temperature. Major-element as well as Ca and Mg isotope profiles were measured on the recovered quenched glasses. In both experiments, Ca diffuses rapidly with respect to Si. In the AB–AN experiment, D{sub Ca}/D{sub Si} ~ 20 and the efficiency of isotope separation for Ca is much greater than in natural liquid experiments where D{sub Ca}/D{sub Si} ~ 1. In the AB–DI experiment, D{sub Ca}/D{sub Si} ~ 6 and the efficiency of isotope separation is between that of the natural liquid experiments and the AB–AN experiment. In the AB–DI experiment, D{sub Mg}/D{sub Si} ~ 1 and the efficiency of isotope separation for Mg is smaller than it is for Ca yet similar to that observed for Mg in natural liquids. The results from the experiments reported here, in combination with results from natural volcanic liquids, show clearly that the efficiency of diffusive separation of Ca isotopes is systematically related to the solvent-normalized diffusivity—the ratio of the diffusivity of the cation (D{sub Ca}) to the diffusivity of silicon (D{sub Si}). The results on Ca isotopes are consistent with available data on Fe, Li, and Mg isotopes in silicate liquids, when considered in terms of the parameter D{sub cation

  10. Is there a geochemical link between volcanic and plutonic rocks in the Organ Mountains caldera? (United States)

    Memeti, V.; Davidson, J.


    determine within-crystal geochemical variations. Our current conclusions and working hypotheses are: 1) All igneous rocks from the Organ Mountains are crustal-mantle melt mixtures indicating two component mixing; 2) the caldera-forming ignimbrites are likely derived from a fractionating Organ Needle pluton; 3) pre- and post-caldera lavas are isotopically similar to the post-caldera Sugarloaf Peak quartz-monzonite; 4) K-feldspar cumulate textures in the structurally top 0.5-1 km of the Organ Needle pluton indicate that interstitial melt was lost from the magma mush, which likely fed the ignimbrite eruptions. 5) Plutonic feldspar textures are complex compared to rather simple zoned volcanic feldspars including K-feldspar rimmed plagioclase, plagioclase rimmed K-feldspar and unrimmed feldspars occurring over a range of grain sizes at thin section scale. Some volcanic feldspar phenocrysts have any previous zonation erased due to late stage albitization. Although the single mineral studies are still work in progress and details need resolving, our data so far suggest a geochemical link between volcanic and plutonic rocks of the Organ Mountains caldera, albeit a complex one; and greater complexity in plutonic versus volcanic minerals. [1] Seager (1980), NM Bureau of Mines and Min. Res. Memoir 36, 97 p. [2] Zimmerer & McIntosh (2013) Journal of Geophysical Research, v. 93, p. 4421-4433

  11. Fluid-Ultramafic Rock Interaction and Formation of Jadeite Rocks%流体一超镁铁质岩相互作用与硬玉岩的形成

    Institute of Scientific and Technical Information of China (English)

    祁敏; 向华; 钟增球; 周汉文


    俯冲带中流体与岩石相互作用以及流体循环一直是地质学家关注的焦点之一.硬玉岩(翡翠)作为高档宝玉石材料,其成因一直备受关注.硬玉岩产于与俯冲带有关的蛇纹石化超镁铁质岩中,是俯冲带中流体与超镁铁岩相互作用的特殊产物.岩石组合、岩相学、显微结构及矿物化学特征表明:橄榄岩与流体的作用可以分为5个阶段,分别为蛇纹石化→(绿泥石、金云母)→角闪石→辉石→(方沸石、钠长石)阶段.结合热力学相图,总结了橄榄岩与流体作用过程中矿物的演化序列.硬玉岩的形成需要富Na、Al、si流体和较高的压力.缅甸硬玉岩中,钠质闪石总是与硬玉岩伴生,钠质闪石成分变化大,且能与流体发生再平衡从而调节自身和流体的成分.钠质闪石在硬玉形成过程中充当了Na、Al、Si的缓冲剂,使Na、Al、Si达到一定比例有利于硬玉的结晶.%The fluid-rock interactions and fluid circulations in subduction zone have been a focus for geologists. As a kind of high-grade gem material, the genesis of jadeite rocks attracts an increasing concern. The jadeite rocks generally occur in the serpentinized ultramafic rocks in subduction zones and its formation is related to the interaction between subduction-related fluids and ultramafic rocks (peridotite). Based on rock association, petrography, microstructure and mineral chemical characteristics, the processes of interaction between peridotite and fluid can be divided into five stages, that is, serpentine→ (chlorite, phlogopite) →amphibole→pyroxene→ (analcime, albite). Combined with analysis of thermodynamic phase diagrams, the evolutionary series of minerals in the processes of interaction are identified. Formation of jadeite requires the fluids enrich in Na, Al, Si and under relatively higher pressure. In the jadeite rocks from Myanmar, the sodium amphiboles with various chemical components are always associated with

  12. Effect of the background solution and material composition on the transport of silver nanoparticles in saturated aquifer materials (United States)

    Adrian, Yorck; Schneidewind, Uwe; Fernandez-Steeger, Tomas; Azzam, Rafig


    Engineered silver nanoparticles (AgNP) are used in various consumer products such as cloth or personal care products due to their antimicrobial properties (Benn et al., 2010). Their transport behavior in the environment is still under investigation. Previous studies have been focusing on the transport of AgNP in simple test systems with glass beads or soil materials (Braun et al., 2015), but studies investigating aquifer material are rare. However, the protection of fresh water resources in the subsurface is an important part in the protection of human health and the assurance of future economic activities. Therefore, expert knowledge regarding the transport and fate of engineered nanoparticles as potential contaminants in aquifers is essential. Within the scope of the research project NanoMobil funded by German Federal Ministry of Education and Research, the transport and retention behavior of AgNP in aquifer material was investigated under saturated conditions in laboratory columns for different flow velocities, ionic strengths (IS) and background solutions. The used aquifer material consisted mainly of quartz and albite. The quartz grains were partially coated with iron hydroxides and oxides. Furthermore, 1% hematite was present in the silicate dominated aquifer material. The experiments were conducted using NaNO3 and Ca(NO3)2 background solutions to examine the effects of monovalent and divalent cations on the transport of AgNP. Flow velocities in the columns were chosen to represent typical flow velocities of groundwater in the subsurface. For the experiments two mean grain sizes of 0.3 and 0.7 mm were used to investigate the effect of the grain size on the transport behavior. Particle concentration was measured using ICP-MS and particle size was determined using flow field-flow fractionation (FlFFF). HYDRUS-1D (Šimůnek et al., 2013) was used to elucidate the transport and retention processes of the AgNP in the aquifer material. The obtained results show

  13. Multi-stage barites in partially melted UHP eclogite: implications for fluid/melt activities during deep continental subduction in the Sulu orogenic belt (United States)

    Wang, Songjie; Wang, Lu


    . Zr-in-rutile thermometry shows their formation temperature to be 586-664 oC at 1.5-2.5 GPa. Barite-bearing MS inclusions with Ba-bearing K-feldspar (type-II) connected by Kfs+Pl+Bt veinlets of in-situ phengite breakdown and thin barite veinlets along grain boundaries (type-III) are products of phengite breakdown and induced fluid flow during exhumation. These barites have witnessed the gradational separation process of melt/ fluid from miscibility on/above the second critical endpoint during UHP metamorphism, to immiscibility along the exhumation path of the subducted slab. Associated reactions from pyrite to hematite and goethite with the type-III barite ring surrounding the pyrite provide evidence for a local high oxygen fugacity environment during eclogite partial melting and subsequent melt/fluid crystallization processes. Moreover, large grain barite aggregations (type-IV) modified by amphibole+albite symplectite are most likely formed by release of molecular and hydroxyl water from anhydrous minerals of eclogite during high-grade amphibolite-facies retrogression. The growth of multi-stage barites in UHP eclogite further advances our understanding of fluid/melt transfer, crystallization processes along the subduction-exhumation path of the partially melted eclogite, broadening our knowledge of melt/fluid evolution within subduction-collision zones worldwide. REFERENCES Chen Y.X., et al., 2014, Lithos, 200, 1-21. Liu J.B., et al., 2000, Acta Petrologica Sinica 16(4), 482-484. Zeng L.S., et al., 2007, Chinese Science Bulletin, 52(21), 2995-3001. Gao X.Y., et al., 2012, Journal of Metamorphic Geology, 30(2), 193-212.

  14. Mineral chemistry and shrimp U-Pb Geochronology of mesoproterozoic polycrase-titanite veins in the sullivan Pb-Zn-Ag Deposit, British Columbia (United States)

    Slack, J.F.; Aleinikoff, J.N.; Belkin, H.E.; Fanning, C.M.; Ransom, P.W.


    Small polycrase-titanite veins 0.1-2 mm thick cut the tourmalinite feeder zone in the deep footwall of the Sullivan Pb-Zn-Ag deposit, southeastern British Columbia. Unaltered, euhedral crystals of polycrase and titanite 50-100 ??m in diameter are variably replaced by a finer-grained alteration-induced assemblage composed of anhedral polycrase and titanite with local calcite, albite, epidote, allanite, and thorite or uranothorite (or both). Average compositions of the unaltered and altered polycrase, as determined by electron-microprobe analysis, are (Y0.38 REE0.49 Th0.10 Ca0.04 Pb0.03 Fe0.01U0.01) (Ti1.48 Nb0.54 W0.04 Ta0.02)O6 and (Y0.42 REE0.32 Th0.15 U0.06 Ca0.04 Pb0.01 Fe0.01) (Ti1.57 Nb0.44 W0.04 Ta0.02)O6, respectively. The unaltered titanite has, in some areas, appreciable F (to 0.15 apfu), Y (to 0.40 apfu), and Nb (to 0.13 apfu). SHRIMP U-Pb geochronology of eight grains of unaltered polycrase yields a weighted 207Pb/206Pb age of 1413 ?? 4 Ma (2??) that is interpreted to be the age of vein formation. This age is 50-60 m.y. younger than the ca. 1470 Ma age of synsedimentary Pb-Zn-Ag mineralization in the Sullivan deposit, which is based on combined geological and geochronological data. SHRIMP ages for altered polycrase and titanite suggest later growth of minerals during the ???1370-1320 Ma East Kootenay and ???1150-1050 Ma Grenvillian orogenies. The 1413 ?? 4 Ma age for the unaltered polycrase in the veins records a previously unrecognized post-ore (1370 Ma) mineralizing event in the Sullivan deposit and vicinity. The SHRIMP U-Pb age of the polycrase and high concentrations of REE, Y, Ti, Nb, and Th in the veins, together with elevated F in titanite and the absence of associated sulfides, suggest transport of these high-field-strength elements (HFSE) by F-rich and S-poor hydrothermal fluids unrelated to the fluids that formed the older Fe-Pb-Zn-Ag sulfide ores of the Sullivan deposit. Fluids containing abundant REE, HFSE, and F may have been derived from a

  15. Effects of Al on mineralogy and kinetics of precipitation of silica minerals under crustal conditions (United States)

    Saishu, H.; Okamoto, A.; Tsuchiya, N.


    Silica is a dominant component in the Earth's crust. Dissolution and precipitation processes of silica minerals play significant roles on the spatial and temporal distributions of fluids and rock strength in the crusts. Quartz veins occur ubiquitously in the vicinity of seismogenic zones. However the rate equation of silica precipitation is important to consider the sealing of fractures by quartz on the earthquake cycle, it has not been determined except for precipitation rates on surface reactions (Rimstidt and Barnes, 1980) because of the following reasons: cristobalite and amorphous silica occur in the geothermal areas (Alekseyev et al., 2009) whereas quartz is stable in the crust, precipitation of silica minerals occurs not only on quartz surfaces but also via nucleation processes in fluids, and trace elements including Al, Na and K in solutions affect on the species and kinetics of silica precipitation (Okamoto et al., 2010). In the crust, feldspars are dominant constituents, thus the effects of these minor components are crucial for considering the silica precipitation. We conducted the hydrothermal flow-through experiments to investigate the overall precipitation rate of silica minerals and the effects of Al in the solutions under crustal conditions (430 °C and 31 MPa). The experimental apparatus is similar to that in Okamoto et al. (2010). A blank vessel without any rock/mineral substrates was used for precipitation of silica minerals. The Si-supersaturated solutions (C/Ceq = 3-3.5) were prepared by dissolution of quartz at 350 °C, and the concentration of Al in the input solution was controlled from 0 to 7 ppm by dissolution of albite with different temperatures. The experiments in pure Si solution revealed that the precipitation via nucleation in fluids was approximated as the third-order reaction whereas the precipitation on the pre-existing quartz surfaces was determined as the first-order reaction in Rimstidt and Barnes (1980). Activation energy of

  16. 镍基高温合金上双层搪瓷-陶瓷复合涂层1000℃氧化机理%Oxidation Behavior of Bilayered Ceramic Particle-reinforced Enamel Composite Coating on Nickel-based Superalloy K38G at 1000 ℃

    Institute of Scientific and Technical Information of China (English)

    沈明礼; 朱圣龙; 王福会


    A bilayered enamel-ceramic composite coating, consisted of an inner layer of enamel-50 mass% corundum and an outer layer of enamel-50 mass% quartz, was prepared on nickel-based superalloy K38G by spray-sintering technique. The coating is dense with glaze surface and has good adhesion to the substrate. Its oxidation behavior at 1000 ℃ for 120 h was studied by means of thermogravimetry, SEM, EDS and XRD. Cristobalite, a high-temperature polymorph of quartz, and zircon and albite precipitates were detected in the as-prepared enamel-ceramic composite coating. In addition, Ni, Co and Cr were present in the inner layer of enamel-corundum. The mass gain of the coated alloy after 120 h oxidation was about 0.2 mg/cm2, quite lower than those of NiCrA1Y coatings. Most of the quartz particles in the coating transformed into cristobalite after oxidation tests. Besides, orthoelase was detected too. Ni-enrichment was observed in the outermost region of the outer layer, while Cr-enrichment was found in the inner layer close to the inner/outer interface. And Ni-, Cr-, Al-enrichment were found in the inner layer near the substrate either of the as-prepared samples or of the samples after oxidation tests.%在镍基高温合金K38G基体上制备了双层搪瓷-陶瓷复合涂层,其中面层为搪瓷-50mass%石英,底层为搪瓷-50mass%刚玉层.涂层结合力良好,表面均匀致密,有釉面光泽.1000℃、120h氧化结果表明,涂层试样的氧化增重仅为0.2mg/cm^2左右,比文献中报道的NiCrAlY涂层的氧化速率低数倍(Ni-22Cr-10Al-1Y(mass%)1000℃100h氧化增重已达1.2mg/cm^2).刚制备出的搪瓷-陶瓷复合涂层中的部分石英颗粒已转变为方石英相,并析出少量的锆英石相和钠长石相.氧化后的涂层中大部分石英颗粒转变成方石英,并析出少量的钾长石相.氧化后的涂层试样中Ni,Cr富集分别出现在涂层的外层靠近空气区域和内层靠近外层

  17. 拉萨地块松多超高压变质带含石榴石云母石英片岩的变质演化相平衡模拟%Phase equilibrium modeling for metamorphic evolution of garnet-bearing mica-quartz schist in Sumdo UHP metamorphic belt, Lhasa Block

    Institute of Scientific and Technical Information of China (English)

    陈梅; 田作林; 张聪; 杨经绥; 黄杰


    岩与榴辉岩经历了相同或者相似的俯冲折返过程。%The garnet-bearing mica-quartz schist of Sumdo UHP belt in Lhasa block occurs as country rocks of eclogite, and is mainly composed of garnet, muscovite, albite, chlorite, quartz and minor rutile and sphene. Garnet displays an obvious compositional zonation where Xprp increases from the core to the mantle and then decreases in the rim, whereas Xsps decreases gradually from the core to mantle, with the trend of declining following rising in the rim, indicating that garnet composition profiles from core to mantle have preserved the prograde growth zoning and were partially reset during retrogression. The model system MnNCKFMASHO was chosen to calculate P-T and P-M(H2O) pseudosections of the garnet-bearing mica-quartz schist. Garnet isopleth thermobarometry involved plotting compositional isopleths of garnet as contours on a P-T pseudosection, with the combination of contours of saturated H2O content, thus obtaining estimated peak P-T conditions of 27 kbar, 523/580℃and peak mineral assemblages of g-jd-cr-law (+phn +q/coe+H2O). The compositional profile of garnet from the core to the mantle and contouring of the H2O content saturated indicate that prograde metamorphic evolution represents a cold subduction stage with heating with the increasing pressure, and the rocks experienced blueschist-facies to eclogite-facies metamorphism during this stage. P-M(H2O) pseudosections and isopleth of saturated H2O content could be used to assess evolution of mineral assemblages in terms of changes in water content during decompression, which shows that garnet-bearing mica quartz schist experienced an early isothermal decompression process and was then followed by a cooling with decompression evolution during the late stage. Amphibolite-facies to epidote-amphibolite-facies metamorphism occurred during early stage and was followed by greenschist-facies metamorphism. The isothermal decompression of garnet-bearing mica-quartz schist probably

  18. CO2 solubility and speciation in rhyolitic sediment partial melts at 1.5-3.0 GPa - Implications for carbon flux in subduction zones (United States)

    Duncan, Megan S.; Dasgupta, Rajdeep


    sediment melt will have the opportunity to dissolve and carry CO2. For hot subduction zones, even if sedimentary layer itself does not carry carbonate, CO2 released from basalt-hosted carbonates may be dissolved in sediment partial melt. Experiments conducted on subducted sediment compositions show that the partial melt compositions are generally rhyolitic (Johnson and Plank, 1999; Hermann and Green, 2001; Schmidt et al., 2004; Auzanneau et al., 2006; Hermann and Spandler, 2008; Spandler et al., 2010; Tsuno and Dasgupta, 2011). Therefore, solubility of CO2 in rhyolitic sediment partial melts needs to be known. Previous studies on rhyolitic melts experimentally determined CO2 solubility from 0.05 to 0.66 GPa (Fig. 1; Fogel and Rutherford, 1990; Blank et al., 1993; Tamic et al., 2001). This pressure range is not appropriate for global sub-arc depth range of 72-173 km (Syracuse and Abers, 2006) settings (P = 2-5 GPa). Carbon dioxide solubility experiments at pressures from 1.5 to 3.5 GPa are available but only on simple compositions - i.e., albite, which does not have the chemical complexity of natural sediment partial melts (Fig. 1; Brey, 1976; Mysen, 1976; Mysen et al., 1976; Mysen and Virgo, 1980; Stolper et al., 1987; Brooker et al., 1999). For example, natural rhyolitic melt derived from partial fusion of pelitic sediments contain non-negligible concentrations of Ca2+, Mg2+, Fe2+. Many of these studies were also conducted under mixed-volatile conditions (CO2 + H2O) with H2O contents from 0.06 to 3.3 wt.%. These studies were used in calculating various solubility models: Volatile-Calc (Newman and Lowenstern, 2002), that of Liu et al. (2005), and that of Papale et al. (2006). Volatile-Calc can be used to calculate CO2 solubility only on a generic rhyolite composition up to 0.5 GPa. The model of Liu et al. (2005) is also on a generic rhyolite up to 0.5 GPa, but can calculate mixed volatile concentrations provided the vapor composition is known. The model of Papale et al

  19. Pseudoseetion modelling of garnet bluesechist from Rongma Area, central Qiangtang,North Tibet:Implications to the tectonic evlution central Qiangtang%西藏羌塘中部绒马地区石榴蓝闪片岩变质演化过程的视剖面模拟及其意义

    Institute of Scientific and Technical Information of China (English)

    刘焰; 吕永增


    Within Qiangtang basin, northern Tibet, a metamorphic belt divides the Qiangtang basin into the northern and southern blocks and was designated as the central Qiangtang metamorphic belt. Although blueschist and eclogite were distinguished within this belt, the tectonic evolution of this metamorphic belt still remains largely debatable. One interpretation is that the central Qiangtang metamorphic belt marks an in-situ palaeo-Tethyan suture zone between.northern Qiangtang terrane of Cathaysian affinity and southern Qiangtang terrane of Gondwana affinity. The alternative argument suggests that the central Qiangtang metamorphic belt was underthrust southward beneath the Qiangtang terrane along the Jinsha suturezone about 200 km in the north. Therefore, the central Qiangtang metamorphic belt did not mark an in-situ suture zone within Qiangtang terrane. Here we investigate the garnet-bearing blueschists from Rongrna area of central Qiangtang in northern Tibet, where is critical to understanding the tectonic evolution of the central Qiangtang metamorphic belt. The mineral assemblage in these rocks is characterized by porphyroblastic garnet set within a matrix of fine-grained amphibole, white mica, epidote, chlorite, albite and quartz with accessory rutile, titanite and apatire. The Mn content of the garnet porphyroblasts decreases from core to rim, whereas the Fe and Mg contents show an increasing trend, respectively. Fine-grained rhomb-shaped inclusions of paragonite and epidote in association with quartz occurring within the core of the garnet porphyroblasts are interpreted as pseudomorphs after lawsonite. Large grains of epidote with inclusions of Na amphibole, rutile and quartz occur in the matrix in contact with the rims of the garnet grains. In the matrix, we identified two stages of Na amphibole rimmed by Na-Ca amphibole and albite. Retrograde chlorite is rimmed by fine-grained biotite. On the basis of microstructural observations and pseudosection modelling, we

  20. Metallogenetic systems associated with granitoid magmatism in the Amazonian Craton: An overview of the present level of understanding and exploration significance (United States)

    Bettencourt, Jorge Silva; Juliani, Caetano; Xavier, Roberto P.; Monteiro, Lena V. S.; Bastos Neto, Artur C.; Klein, Evandro L.; Assis, Rafael R.; Leite, Washington Barbosa, Jr.; Moreto, Carolina P. N.; Fernandes, Carlos Marcello Dias; Pereira, Vitor Paulo


    íder and Teles Pires suites). The Transamazonas Province corresponds to a N-S-trending orogenic belt, consolidated during the Transamazonian cycle (2.26-1.95 Ga), comprising the Lourenço, Amapá, Carecuru, Bacajá, and Santana do Araguaia tectonic domains. They show a protracted tectonic evolution, and are host to the pre-, syn-, and post-orogenic to anorogenic granitic magmatism. Gold mineralization associated with magmatic events is still unclear. Greisen and pegmatite Sn-Nb-Ta deposits are related to 1.84 to 1.75 Ga late-orogenic to anorogenic A-type granites. The Pitinga Tin Province includes the Madeira Sn-Nb-Ta-F deposit, Sn-greisens and Sn-episyenites. These are associated with A-type granites of the Madeira Suite (1.84-1.82 Ga), which occur within a cauldron complex (Iricoumé Group). The A-type magmatism evolved from a post-collisional extension, towards a within-plate setting. The hydrothermal processes (400 °C-100 °C) resulted in albitization and formation of disseminated cryolite, pyrochlore columbitization, and formation of a massive cryolite deposit in the core of the Madeira deposit. The Rondônia Tin Province hosts rare-metal (Ta, Nb, Be) and Sn-W mineralization, which is associated with the São Lourenço-Caripunas (1.31-1.30 Ga), related to the post-collisional stage of the Rondônia San Ignácio Province (1.56-1.30 Ga), and to the Santa Clara (1.08-1.07 Ga) and Younger Granites of Rondônia (0.99-0.97 Ga) A-type granites. The latter are linked to the evolution of the Sunsás-Aguapeí Province (1.20-0.95 Ga). Rare-metal polymetallic deposits are associated with late stage peraluminous granites, mainly as greisen, quartz vein, and pegmatite types.

  1. Batievaite-(Y), Y2Ca2Ti[Si2O7]2(OH)2(H2O)4, a new mineral from nepheline syenite pegmatite in the Sakharjok massif, Kola Peninsula, Russia (United States)

    Lyalina, L. M.; Zolotarev, A. A.; Selivanova, E. A.; Savchenko, Ye. E.; Krivovichev, S. V.; Mikhailova, Yu. A.; Kadyrova, G. I.; Zozulya, D. R.


    Batievaite-(Y), Y2Ca2Ti[Si2O7]2(OH)2(H2O)4, is a new mineral found in nepheline syenite pegmatite in the Sakharjok alkaline massif, Western Keivy, Kola Peninsula, Russia.