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Sample records for accurate sr isotope

  1. Investigation of a dynamic seawater intrusion event using strontium isotopes (87Sr/86Sr)

    DEFF Research Database (Denmark)

    Jørgensen, Niels Oluf; Andersen, Martin S.; Engesgaard, Peter Knudegaard

    2008-01-01

    isotopes reflect recharge conditions and mixing between groundwater and seawater. The 87Sr/86Sr isotope ratios are controlled by aquifer matrix chemistry. The 87Sr/86Sr ratio distribution and Sr content reveal a ternary mixing system in the shallow aquifer, encompassing brackish seawater, fresh shallow...... of Palaeocene (Danian) limestone. Stable isotopes (18O and 2H), strontium isotopes (87Sr/86Sr) and the elements Sr and Cl were measured to delineate the mixing of seawater and groundwater in the shallow aquifer and to determine the contribution from different water sources along the flow paths. The stable...

  2. Genesis of Sr Isotopes in Groundwater of Hebei Plain

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    To analyze the genesis of Sr isotopes in groundwater of Hebei plain, time-accumulative effect of 87Sr/86Sr ratio was studied. It is shown that 87Sr/86Sr ratio increases with the increasing age and depth of groundwater and has a positive correlation to 4Heexc and a negative correlation to δ18O and δD.The groundwater is divided into three groups to discuss the relation between 87Sr/86Sr ratio and Sr2+ content: ① moderate Sr2+ content and higher 87Sr/86Sr ratio (water Ⅰ); ② lower Sr2+ content and higher 87Sr/86Sr ratio (water Ⅱ); and ③ higher Sr2+ content and lower 87Sr/86Sr ratio (water Ⅲ), that is hot water. On the basis of integrated analysis, it was considered that ① the radiogenic Sr in the Quaternary groundwater (Q4-Q1) originates from weathering of silicate rich in Na and Rb, mainly from plagioclase; ② the radiogenic Sr of hot water in Huanghua port is attributed to carbonate dissolution, with lower 87Sr/86Sr ratio and higher Sr/Na ratio; ③ the recharge area is laterally recharged by the groundwater flowing through igneous and metamorphic rocks, with moderate 87Sr/86Sr ratio. However, the formation mechanism of Sr isotopes in Tertiary groundwater needs further studies.

  3. Estimating the distribution of strontium isotope ratios (87Sr/86Sr in the Precambrian of Finland

    Directory of Open Access Journals (Sweden)

    Lars Kaislaniemi

    2011-12-01

    Full Text Available A method to estimate the 87Sr/86Sr ratio of a rock based on its age and Rb/Sr ratio is presented. This method, together with data from the Rock Geochemical Database of Finland (n=6544 is used to estimate the 87Sr/86Sr ratios in the Precambrian of Finland and in its different major units. A generalization to cover the whole area of Finland is achieved by smoothing of estimation points. The estimation method is evaluated by comparing its results to published Rb-Sr isotope analyses (n=138 obtained on the Finnish Precambrian. The results show correspondence to different geological units of Finland,but no systematic difference between Archaean and younger areas is evident. Evaluation of the method shows that most of the estimates are reliable and accurate to be used as background material for provenance studies in archaeology, paleontology and sedimentology. However, some granitic rocks may have large (>1.0 % relative errors.Strontium concentration weighted average of the estimates differs only by 0.001 from the average 87Sr/86Sr ratio (0.730 of the rivers on the Fennoscandian shield.

  4. Accurate hydrocarbon estimates attained with radioactive isotope

    International Nuclear Information System (INIS)

    To make accurate economic evaluations of new discoveries, an oil company needs to know how much gas and oil a reservoir contains. The porous rocks of these reservoirs are not completely filled with gas or oil, but contain a mixture of gas, oil and water. It is extremely important to know what volume percentage of this water--called connate water--is contained in the reservoir rock. The percentage of connate water can be calculated from electrical resistivity measurements made downhole. The accuracy of this method can be improved if a pure sample of connate water can be analyzed or if the chemistry of the water can be determined by conventional logging methods. Because of the similarity of the mud filtrate--the water in a water-based drilling fluid--and the connate water, this is not always possible. If the oil company cannot distinguish between connate water and mud filtrate, its oil-in-place calculations could be incorrect by ten percent or more. It is clear that unless an oil company can be sure that a sample of connate water is pure, or at the very least knows exactly how much mud filtrate it contains, its assessment of the reservoir's water content--and consequently its oil or gas content--will be distorted. The oil companies have opted for the Repeat Formation Tester (RFT) method. Label the drilling fluid with small doses of tritium--a radioactive isotope of hydrogen--and it will be easy to detect and quantify in the sample

  5. Estimating the distribution of strontium isotope ratios (87Sr/86Sr) in the Precambrian of Finland

    OpenAIRE

    Lars Kaislaniemi

    2011-01-01

    A method to estimate the 87Sr/86Sr ratio of a rock based on its age and Rb/Sr ratio is presented. This method, together with data from the Rock Geochemical Database of Finland (n=6544) is used to estimate the 87Sr/86Sr ratios in the Precambrian of Finland and in its different major units. A generalization to cover the whole area of Finland is achieved by smoothing of estimation points. The estimation method is evaluated by comparing its results to published Rb-Sr isotope analyses (n=138) obta...

  6. Origins of invasive piscivores determined from the strontium isotope ratio (87Sr/86Sr) of otoliths

    Science.gov (United States)

    Wolff, Brian A.; Johnson, Brett M.; Breton, Andre R.; Martinez, Patrick J.; Winkelman, Dana L.; Gillanders, Bronwyn

    2012-01-01

    We examined strontium isotope ratios (87Sr/86Sr) in fish otoliths to determine the origins of invasive piscivores in the Upper Colorado River Basin (UCRB, western USA). We examined 87Sr/86Sr from fishes in different reservoirs, as well as the temporal stability and interspecies variability of 87Sr/86Sr of fishes within reservoirs, determined if 87Sr/86Sr would be useful for "fingerprinting" reservoirs where invasive piscivores may have been escaping into riverine habitat of endangered fishes in the UCRB, and looked for evidence that such movement was occurring. Our results showed that in most cases 87Sr/86Sr was unique among reservoirs, overlapped among species in a given reservoir, and was temporally stable across years. We identified the likely reservoir of origin of river-caught fish in some cases, and we were also able to determine the year of possible escapement. The approach allowed us to precisely describe the 87Sr/86Sr fingerprint of reservoir fishes, trace likely origins of immigrant river fish, and exclude potential sources, enabling managers to focus control efforts more efficiently. Our results demonstrate the potential utility of 87Sr/86Sr as a site-specific and temporally stable marker for reservoir fish and its promise for tracking fish movements of invasive fishes in river-reservoir systems.

  7. Resolving archaeological populations with Sr-isotope mixing models

    International Nuclear Information System (INIS)

    Strontium isotope analysis of tooth enamel is a useful provenancing technique to investigate the childhood origins and residential mobility of ancient people. However, where different geographical target regions have similar biosphere 87Sr/86Sr it is often difficult to resolve the 87Sr/86Sr ranges of two different groups of people and establish what constitutes the local range at each site. Here a multi-period study is presented from the Outer Hebrides, Scotland and an investigation of Neolithic and Early Bronze Age populations from the Yorkshire Wolds, NE England. The aim is to demonstrate that, despite complex human dietary strategies, simple mixing systems with only two end-members do occur in archaeological human populations in certain geological provinces and, despite overlapping 87Sr/86Sr ranges, it is possible to separate two populations based on the structure within the data set

  8. An analytical approach to Sr isotope ratio determination in Lambrusco wines for geographical traceability purposes.

    Science.gov (United States)

    Durante, Caterina; Baschieri, Carlo; Bertacchini, Lucia; Bertelli, Davide; Cocchi, Marina; Marchetti, Andrea; Manzini, Daniela; Papotti, Giulia; Sighinolfi, Simona

    2015-04-15

    Geographical origin and authenticity of food are topics of interest for both consumers and producers. Among the different indicators used for traceability studies, (87)Sr/(86)Sr isotopic ratio has provided excellent results. In this study, two analytical approaches for wine sample pre-treatment, microwave and low temperature mineralisation, were investigated to develop accurate and precise analytical method for (87)Sr/(86)Sr determination. The two procedures led to comparable results (paired t-test, with twine sample), processed during each sample batch (calculated Relative Standard Deviation, RSD%, equal to 0.002%. Lambrusco PDO (Protected Designation of Origin) wines coming from four different vintages (2009, 2010, 2011 and 2012) were pre-treated according to the best procedure and their isotopic values were compared with isotopic data coming from (i) soils of their territory of origin and (ii) wines obtained by same grape varieties cultivated in different districts. The obtained results have shown no significant variability among the different vintages of wines and a perfect agreement between the isotopic range of the soils and wines has been observed. Nevertheless, the investigated indicator was not enough powerful to discriminate between similar products. To this regard, it is worth to note that more soil samples as well as wines coming from different districts will be considered to obtain more trustworthy results.

  9. Disturbed Sr and Nd Isotope Systematics in Zircons With Concordant SHRIMP U-Pb Ages

    Science.gov (United States)

    Weaver, K. L.; Bennett, V. C.; Depaolo, D. J.; Mundil, R.

    2004-12-01

    Little is known about the Sr- and Nd-isotopic systematics of zircon. With slow diffusion rates and a high resistance to weathering, zircon should preserve accurate age information and initial Sr and Nd isotopic ratios. As a common accessory mineral, it could provide petrogenetic information for rocks that have been altered, weathered, or metamorphosed. We have investigated the Sm-Nd and Rb-Sr systematics of zircons from unmetamorphosed granitic rocks that have yielded concordant U-Pb SHRIMP (Sensitive High Resolution Ion Microprobe) ages and have depleted mantle signatures for Nd and Sr isotopes. Zircon populations from mantle-derived igneous rocks with ages of 0.1, 1.7, and 3.8 Ga were chosen for Sr and Nd isotopic analysis. Low concentrations (Sr, 4 to 8 ppm and Nd, 6 to 12 ppm) and small grain size necessitate the use of multigrain aliquots. Meaningful results can be obtained only if all of the zircons in the rock are a coherent population with homogeneous ages throughout and among grains. Zircon U-Pb ages were characterized using the SHRIMP RG, and trace element concentrations were measured by LA-ICPMS. The populations are homogeneous and the material ablated by the ion beam ( ˜~20 μ m spot size) shows little evidence of lead loss. Results on zircons of 100 Ma and 1700 Ma indicate that both the Rb-Sr and Sm-Nd systems have been severely disturbed. For the 1700 Ma granitic rocks from the Yavapai sequence of Arizona, zircon Sm-Nd apparent ages are ca. 1000 Ma! Leaching was used to remove contributions from adhering or included minerals, but leached residues that presumably most closely approximate the composition of the pure zircon (e.g. have high Sm/Nd) are no less disturbed than unleached samples. Despite the U-Pb SHRIMP ages indicating a closed system, the zircons have failed to preserve a reasonable age or initial isotopic composition for Sr and Nd, indicating that parts of the crystal might be severely affected by radiation damage resulting in disturbed

  10. {sup 87}Sr/{sup 86}Sr isotope fingerprinting of Scottish and Icelandic migratory shorebirds

    Energy Technology Data Exchange (ETDEWEB)

    Evans, Jane, E-mail: je@bgs.ac.uk [NERC Isotope Geosciences Laboratory, Keyworth, Nottingham, NG12 5GG (United Kingdom); Bullman, Rhys [Scottish Natural Heritage, Beta Centre, Innovation Park, University of Stirling, Stirling, FK9 4LA (United Kingdom)

    2009-10-15

    Biosphere Sr isotope composition data from Iceland and Scotland suggest that terrestrially feeding birds from these two countries will have significantly different {sup 87}Sr/{sup 86}Sr isotope composition in their tissues. The aim of this study is to test if these differences can be measured within the bone and feather of migratory wading birds, who feed terrestrially as juveniles, thus providing a provenance tool for these birds. The study shows that birds can be distinguished on the basis of the Sr isotope composition of their bone. The field for Icelandic birds is defined by data from juvenile common redshank (Tringa totanus) and whimbrel (Numenius phaeopus) which give 0.7056 {+-} 0.0012, (2{sigma}, n = 7). The majority of Scottish birds in this study are from coastal regions and have a signature close to that of seawater of 0.7095 {+-} 0.0006 (2{sigma}, n = 9). The Sr ratios in the body tissue of these two populations of all Icelandic and Scottish adult and juvenile birds analysed are significantly different (p < 0.001, at 95% confidence limits). Scottish birds from inland areas such as a common snipe (Gallinago gallinago) record {sup 87}Sr/{sup 86}Sr values as high as 0.7194 which reflect their non-marine diet. Icelandic redshank (Tringa totanus robusta) that have flown to Scotland and returned to Iceland show the effect of the Scottish contribution to their diet with elevated values of 0.7086 {+-} 0.0004, (2{sigma}, n = 6). Redshank found in Scotland that cannot be classified on the basis biometric analysis are shown to be of Icelandic origin and analysis of the primary feathers from two birds demonstrates that isotope variation between feathers could be used to track changes in diet related to the timing of individual feather growth.

  11. Sr - an element shows the way - Applications of Sr isotopes for provenance, tracing and migration (Invited)

    Science.gov (United States)

    Prohaska, T.; Irrgeher, J.; Zitek, A.; Teschler Nicola, M.

    2010-12-01

    Strontium - named after the small Scottish town Strontian - as such is an element with little popularity. Firstly described by Martin Heinrich Klaproth in 1798, the metal is used in metallurgy to some extent whereas its compounds are interesting in glass industries, electronics and pyrotechnics. The element has chemical similarity to Ca and makes up 1/60 of the earth’s amount of the latter. Nonetheless, it is its isotopic composition which makes Sr so interesting for a large number of scientists. The natural composition of the four naturally occurring isotopes (84Sr, 86Sr 87Sr and 88Sr) varies in nature due to the radioactive decay of 87Rb to 87Sr. Thus, it was early recognized as geochronometer especially in Ca rich matrices. With increasing precision of applied methodology, the natural variation of the 87Sr/86Sr isotope ratio (analyzed at first mainly by thermal ionization mass spectrometry (TIMS)) became more and more popular in provenance studies. The natural variation of the ratio is mainly determined by the geological age and the original composition of the rock and can be used therefore as fingerprint of the local geology. The ratio is transferred with no significant fractionation via the water into plants and finally via the food chain into animal and human tissues (especially bones and teeth). As the element is chemically similar to Ca, it appears in most matrices. The use for provenance studies is supported by the fact that the long half life (4.8 x 1010 years) does not lead to an alteration during the time scales which are investigated (from recent samples to human or animal skeletal remains which date back up to 30.000 BC). The uniqueness of the system besides the natural variation is defined by the ubiquity in nature and the relatively high (and thus measurable) elemental concentration in most tissues. It was finally the advent of multiple collector inductively coupled plasma mass spectrometry (MC-ICP-MS) which augmented the number of applications

  12. An accurate DNA marker assay for stem rust resistance gene Sr2 in wheat

    Science.gov (United States)

    The stem rust resistance gene Sr2 has provided broad-spectrum protection against stem rust (Puccinia graminis) since its wide spread deployment in wheat from the 1940s. Because Sr2 confers partial resistance which is difficult to select under field conditions, a DNA marker is desirable that accurate...

  13. Accurate mass measurements on neutron-deficient krypton isotopes

    CERN Document Server

    Rodríguez, D; Äystö, J; Beck, D

    2006-01-01

    The masses of $^{72–78,80,82,86}$Kr were measured directly with the ISOLTRAP Penning trap mass spectrometer at ISOLDE/CERN. For all these nuclides, the measurements yielded mass uncertainties below 10 keV. The ISOLTRAP mass values for $^{72–75}$Kr being more precise than the previous results obtained by means of other techniques, and thus completely determine the new values in the Atomic-Mass Evaluation. Besides the interest of these masses for nuclear astrophysics, nuclear structure studies, and Standard Model tests, these results constitute a valuable and accurate input to improve mass models. In this paper, we present the mass measurements and discuss the mass evaluation for these Kr isotopes.

  14. Sr fluxes and isotopic compositions of the eleven rivers originating from the Qinghai-Tibet Plateau and their contributions to 87Sr/86Sr evolution of seawater

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    To evaluate influence of chemical weathering of the Qinghai-Tibet Plateau (QTP) on seawater 87Sr/86Sr variation, river water and sediment samples were collected, and their Sr concentrations and isotopic compositions analyzed, from the seven large rivers that originated from the QTP. By combining these with the data of the Ganges, Brahmaputra, Indus and Irrawaddy originated in the southern QTP, the total Sr flux of the eleven rivers reaches 3.47×109 mol·a-1, which accounts for 10.2% of the total Sr flux transported by the global rivers. The weighted mean 87Sr/86Sr is 0.71694, higher than the average value of the global rivers. The 87Srex (87Sr flux in excess of the seawater 87Sr/86Sr ratio) of the Chinese seven rivers is 1.55×106 mol·a-1, only accounting for about 6% of the value of the eleven rivers originated from QTP, and the Ganges-Brahmaputra system accounts for 86%. We assume that the QTP rivers have no strontium contributions to the oceans before ~40 Ma and the Sr fluxes of the global rivers, except the QTP eleven rivers, are constant, then a maximum linear increase in Sr fluxes of the QTP rivers from zero to the modern value in response to tectonic uplift can explain ~69% increase of seawater 87Sr/86Sr over the past ~40 Ma and the remainder of 31% is perhaps provided from other factors.

  15. Sr isotope evolution during chemical weathering of granites -- impact of relative weathering rates of minerals

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The Sr isotopic systematics in the weathering profiles of biotite granite and granite porphyry in southern Jiangxi Province were investigated. The results showed that during the chemical weathering of granites, remarked fractionation occurred between Rb and Sr. During the early stages of chemical weathering of granites, the released Sr/Si and Sr/Ca ratios are larger than those of the parent rocks, and the leaching rate of Sr is higher than those of Si, Ca, K, Rb, etc. Dynamic variations in relative weathering rates of the main Sr-contributing minerals led to fluctuation with time in 87Sr/86Sr ratios of inherent and released Sr in the weathering crust of granite. Successive weathering of biotite, plagioclase and K-feldspar made 87Sr/86Sr ratios in the weathering residues show such a fluctuation trend as to decrease first, increase, and then decrease again till they maintain stable. This work further indicates that when Sr isotopes are used to trace biogeochemical processes on both the catchment and global scales, one must seriously take account of the prefer-ential release of Sr from dissolving solid phase and the fluctuation of 87Sr/86Sr ratios caused by the variations of relative weathering rates of Sr-contributing minerals.

  16. Variability of carbonate diagenesis in equatorial Pacific sediments deduced from radiogenic and stable Sr isotopes

    Science.gov (United States)

    Voigt, Janett; Hathorne, Ed C.; Frank, Martin; Vollstaedt, Hauke; Eisenhauer, Anton

    2015-01-01

    The recrystallisation (dissolution-precipitation) of carbonate sediments has been successfully modelled to explain profiles of pore water Sr concentration and radiogenic Sr isotope composition at different locations of the global ocean. However, there have been few systematic studies trying to better understand the relative importance of factors influencing the variability of carbonate recrystallisation. Here we present results from a multi-component study of recrystallisation in sediments from the Integrated Ocean Drilling Program (IODP) Expedition 320/321 Pacific Equatorial Age Transect (PEAT), where sediments of similar initial composition have been subjected to different diagenetic histories. The PEAT sites investigated exhibit variable pore water Sr concentrations gradients with the largest gradients in the youngest sites. Radiogenic Sr isotopes suggest recrystallisation was relative rapid, consistent with modelling of other sediment columns, as the 87Sr/86Sr ratios are indistinguishable (within 2σ uncertainties) from contemporaneous seawater 87Sr/86Sr ratios. Bulk carbonate leachates and associated pore waters of Site U1336 have lower 87Sr/86Sr ratios than contemporaneous seawater in sediments older than 20.2 Ma most likely resulting from the upward diffusion of Sr from older recrystallised carbonates. It seems that recrystallisation at Site U1336 may still be on-going at depths below 102.5 rmcd (revised metres composite depth) suggesting a late phase of recrystallisation. Furthermore, the lower Sr/Ca ratios of bulk carbonates of Site U1336 compared to the other PEAT sites suggest more extensive diagenetic alteration as less Sr is incorporated into secondary calcite. Compared to the other PEAT sites, U1336 has an inferred greater thermal gradient and a higher carbonate content. The enhanced thermal gradient seems to have made these sediments more reactive and enhanced recrystallisation. In this study we investigate stable Sr isotopes from carbonate-rich deep

  17. 87Sr/86Sr isotope ratio measurements by laser ablation multicollector inductively coupled plasma mass spectrometry: Reconsidering matrix interferences in bioapatites and biogenic carbonates

    Science.gov (United States)

    Irrgeher, Johanna; Galler, Patrick; Prohaska, Thomas

    2016-11-01

    This study is dedicated to the systematic investigation of the effect of interferences on Sr isotopic analyses in biological apatite and carbonate matrices using laser ablation multicollector inductively coupled plasma mass spectrometry (LA-MC ICP-MS). Trends towards higher 87Sr/86Sr ratios for LA-MC ICP-MS compared to solution-nebulization based MC ICP-MS when analysing bioapatite matrices (e.g. human teeth) and lower ratios in case of calcium carbonates (e.g. fish ear stones) were observed. This effect can be related to the presence of significant matrix-related interferences such as molecular ions (e.g. (40Ca-31P-16O)+, (40Ar-31P-16O)+, (42Ca-44Ca)+, (46Ca40Ar)+) as well as in many cases concomitant atomic ions (e.g. 87Rb+, 174Hf2 +). Direct 87Sr/86Sr ratio measurements in Ca-rich samples are conducted without the possibility of prior sample separation, which can be accomplished routinely for solution-based analysis. The presence of Ca-Ar and Ca-Ca molecular ion interferences in the mass range of Sr isotopes is shown using the mass resolving capabilities of a single collector inductively coupled plasma sector field mass spectrometer operated in medium mass resolution when analysing bioapatites and calcium carbonate samples. The major focus was set on analysing human tooth samples, fish hard parts and geological carbonates. Potential sources of interferences were identified and corrected for. The combined corrections of interferences and adequate instrumental isotopic fractionation correction procedures lead to accurate data even though increased uncertainties have to be taken into account. The results are discussed along with approaches presented in literature for data correction in laser ablation analysis.

  18. Pb and Sr isotopic compositions of ancient pottery: a method to discriminate production sites

    International Nuclear Information System (INIS)

    The discriminating of production sites of ancient pottery samples using multi-isotopic systematics was described. Previous work has proven that Pb isotopic ratios can be used for discriminating the production sites of ancient pottery under certain conditions. The present work suggests that although Nd isotopic ratios are not sensitive to the production sites of ancient pottery, Sr isotopic ratios are important for the purpose. Pb isotopic ratios are indistinguishable for the pottery excavated from the Jiahu relict, Wuyang, Henan Province and for famous Qin Terra-cotta Figures. But, the 87Sr/86Sr ratios for the former (about 0.715) are significantly lower than that of the latter (0.717-0.718). The authors concluded that a combined use of Pb and Sr isotopes would be a more powerful method for discriminating the production site of ancient pottery. (authors)

  19. The exploration of Sr isotopic analysis applied to Chinese glazes: part one

    OpenAIRE

    Ma, Hongjiao; Henderson, Julian; Evans, Jane

    2014-01-01

    Ash glaze and limestone glaze are two major glaze types in southern Chinese ceramic technology. In this study strontium isotope compositions were determined in ash glaze samples from the Yue kiln dated to between the 10th and 12th centuries AD, limestone glaze samples from Jingdezhen dated to between the 15th and 18th centuries AD and ceramic raw materials from Jingdezhen. The Sr isotopic characteristics of limestone glaze and ash glaze are completely different. The Sr isotope characteristics...

  20. Sr-Nd ISOTOPES IN MOSSES FROM ROMAGNA (ITALY) AND THEIR ENVIRONMENTAL SIGNIFICANCE

    OpenAIRE

    Francesca Castorina; Umberto Masi

    2010-01-01

    Sr-Nd isotopes were applied for the first time to the study of several moss samples from a transect stretching through Romagna from the Apennines to the Adriatic sea coast. The isotopic data suggest that the mosses uptake Sr and Nd via atmospheric depositions from both marine carbonates and old siliceous crustal rocks. Anthropic pollution cannot be precisely evaluated because of the lack of univocal isotopic signature of the sources.

  1. Sr-Nd ISOTOPES IN MOSSES FROM ROMAGNA (ITALY AND THEIR ENVIRONMENTAL SIGNIFICANCE

    Directory of Open Access Journals (Sweden)

    Francesca Castorina

    2010-04-01

    Full Text Available Sr-Nd isotopes were applied for the first time to the study of several moss samples from a transect stretching through Romagna from the Apennines to the Adriatic sea coast. The isotopic data suggest that the mosses uptake Sr and Nd via atmospheric depositions from both marine carbonates and old siliceous crustal rocks. Anthropic pollution cannot be precisely evaluated because of the lack of univocal isotopic signature of the sources.

  2. Sr isotopic variations in Upper Proterozoic carbonates from Svalbard and East Greenland

    Science.gov (United States)

    Derry, Louis A.; Keto, Lisette S.; Jacobsen, Stein B.; Knoll, Andrew H.; Swett, Keene

    1989-01-01

    Precambrian Sr isotope stratigraphy was investigated by determining variations in Sr-87/Sr-86 ratios in the Upper Proterozoic carbonate succession from Svalbard and East Greenland. Data from this study were combined with those from literature to construct a curve of Sr-87/Sr-86 versus time for Upper Proterozoic seawater. The curve for the Upper Riphean-Vandian showed that the isotopic composition of Sr in seawater was low (Delta Sr-87 of about -500) between 900 and 650 Ma but rose rapidly to about +30 by 600 Ma (this range of long-term variation exceeds the total Phanerozoic variation). The very low values of Delta Sr-87 inferred for the Riphean require that, for this time, the submarine hydrothermal water flux was a large fraction of the Sr input to the oceans, while the rise in Delta Sr-87 in the Upper Proterozoic seawater reflects both a change in the ratio of hydrothermal and continental fluxes of Sr to the oceans, and a change in the isotopic composition of Sr from continental sources.

  3. Sr isotopes in the Orgueil CI meteorite: Chronology of early solar system hydrothermal activity

    Indian Academy of Sciences (India)

    J D Macdougall

    2000-03-01

    New Sr isotopic analyses and calculated formation ages of carbonates from the Orgueil CI meteorite are reported. Among the samples analyzed in this work, dolomites give the youngest formation ages and may have been deposited intermittently starting near the time of parent body formation and continuing for at least 30 Ma. The Sr isotope data also suggest that breunnerites (Fe-Mn-Mg carbonates) crystallized after dolomite formation. Leaching experiments on bulk meteorite samples provide evidence for a very mobile, water soluble Sr reservoir in Orgueil that is characterized by extremely radiogenic Sr (87Sr/86Sr ≈ 0.81- 0.82). This unsupported Sr reflects recent element redistribution, possibly at the time of parent body breakup recorded by the ∼10 Ma exposure age of Orgueil. The carbonate data in particular corroborate earlier indications that hydrothermal processes were among the earliest events to affect the CI parent body.

  4. Sr fluxes and isotopic compositions of the eleven rivers originating from the Qinghai-Tibet Plateau and their contributions to 87Sr/86Sr evolution of seawater

    Institute of Scientific and Technical Information of China (English)

    WU WeiHua; YANG JieDong; XU ShiJin; LI GaoJun; YIN HongWei; TAO XianCong

    2009-01-01

    To evaluate influence of chemical weathering of the Qinghai-Tibet Plateau (QTP) on seawater 87Sr/66Srvariation, river water and sediment samples were collected, and their Sr concentrations and isotopic compositions analyzed, from the seven large rivers that originated from the QTP. By combining these with the data of the Ganges, Brahmaputra, Indus and Irrawaddy originated in the southern QTP, the total transported by the global rivers. The weighted mean 87Sr/86Sr is 0.71694, higher than the average value of the global rivers. The 87Srex (87Sr flux in excess of the seawater 87Sr/66Sr ratio) of the Chinese seven QTP, and the Ganges-Brahmaputra system accounts for 86%. We assume that the QTP rivers have no strontium contributions to the oceans before -40 Ma and the Sr fluxes of the global rivers, except the QTP eleven rivers, are constant, then a maximum linear increase in Sr fluxes of the QTP rivers from zero to the modern value in response to tectonic uplift can explain -69% increase of seawater 87Sr/86Sr over the past -40 Ma and the remainder of 31% is perhaps provided from other factors.

  5. Shape coexistence in neutron-rich Sr isotopes : Coulomb excitation of $^{96}$Sr

    CERN Multimedia

    Clement, E; Siem, S; Czosnyka, T

    2007-01-01

    The nuclei in the mass region A $\\cong$ 100 around Sr and Zr show a dramatic change of the nuclear ground-state shape from near spherical for N $\\leq$ 58 to strongly deformed for N $\\geq$ 60. Theoretical calculations predict the coexistence of slightly oblate and strongly prolate deformed configurations in the transitional region. However, excited rotational structures based on the highly deformed configuration, which becomes the ground state at N = 60, are not firmly established in the lighter isotopes, and the earlier interpretation of a very abrupt change of shape has been challenged by recent experimental results in favor of a rather gradual change. We propose to study the electromagnetic properties of the neutron-rich nucleus $_{38}^{96}$Sr$_{58}$ by low-energy Coulomb excitation using the REX-ISOLDE facility and the MINIBALL detector array. Both transitional and diagonal matrix elements will be extracted, resulting in a complete description of the transition strengths and quadrupole moments of the low-l...

  6. Isotopic equilibration during partial melting: an experimental test of the behaviour of Sr

    Science.gov (United States)

    Hammouda, T.; Pichavant, M.; Chaussidon, M.

    1996-10-01

    Experiments using isotopically enriched, Sr doped minerals designed to test for isotopic equilibrium between source and melt during partial melting reveal that 87Sr/ 86Sr ratios of the liquids are primarily determined by the proportions of minerals consumed and vary with the advancement of the melting reaction. The experiments were performed at 1 atm on model crustal assemblages composed of pairs of natural plagioclase (An 68; 87Sr/ 86Sr= 0.701 ) and synthetic fluorphlogopite doped with 90 ppm Sr having 87Sr/ 86Sr= 4.2 . SIMS traverses showed that during the initial stages of the reaction, liquids are isotopically zoned. All the analyzed melts have 87Sr/ 86Sr markedly higher than that of the bulk starting assemblage (i.e. the source), because of the faster melting rate of fluorphlogopite. At 1200°C and 1250°C melting occurs above a critical temperature, wherein the dissolution rates of the crystals are controlled by diffusion of species in the melt, and reactants and reaction products are out of isotopic equilibrium. This is due to faster melt-crystal boundary migration when compared to Sr diffusion in the crystals. Equilibration is possible only if melting stops. Calculations show that total equilibration between melt and residue by Sr tracer diffusion in the crystals takes 10 4-10 6 yr (for temperature and grain size ranging, respectively, from 800°C to 1000°C, and 0.1 to 1 cm). When compared to the proposed residence time of crustal magmas at their sources, this result strongly suggests that magmas that do not reflect the bulk isotopic characteristics of their source regions can be produced.

  7. Rapid accurate isotopic measurements on boron in boric acid and boron carbide.

    Science.gov (United States)

    Duchateau, N L; Verbruggen, A; Hendrickx, F; De Bièvre, P

    1986-04-01

    A procedure is described whereby rapid and accurate isotopic measurements can be performed on boron in boric acid and boron carbide after fusion of these compounds with calcium carbonate. It allows the determination of the isotopic composition of boron in boric acid and boron carbide and the direct assay of boron or the (10)B isotope in boron carbide by isotope-dilution mass spectrometry.

  8. Sr isotopes and U series radionuclides in the Sangemini area (Central Italy: Hydrogeology implications

    Directory of Open Access Journals (Sweden)

    Maurizio Barbieri

    2014-06-01

    Full Text Available The strontium isotopic ratio (expressed as 87Sr/86Sr of groundwater represents a useful method for studying and understanding the groundwater circulations, also, the U and Ra isotopic compositions can vary as function of the groundwater residence time. This paper reports an evaluation of the probable recharge area of the Sangemini mineral water springs (Terni-Umbria Central Italy and an estimate of the residence time of the aquifer by coupling Sr and U series isotopic systematics. For this study have been analyzed four water sample for the isotope ratio of 87Sr/86Sr, and eleven samples, shallow waters and groundwaters, for U and Ra, furthermore were determined the values of isotopic ratio for sample of typical rocks of the area. The results of this study allow to identify: a recharge area in a restricted sector of the Meso-Cenozoic carbonates a longer and more effective water/rock interaction in the Quaternary series. U and Ra recoil models allow to estimate a groundwater residence time of about 350 years and a total water volume whose value (64*106 m3 agrees with the limited extension of the aquifer. The extension of the aquifer was constrained by comparing Sr isotopic composition of waters and local geological formations. Groundwaters seem mainly to circulate in clayey sandy Quaternary series characterized by low redox conditions.

  9. A change of Sr cycle in the Ediacaran Ocean: Evidence from radiogenic and stable isotope ratios of Sr, in Three Gorges, South China.

    Science.gov (United States)

    Sawaki, Y.; Tahata, M.; Komiya, T.; Maruyama, S.

    2008-12-01

    Objective. To decode surface environmental changes and patterns of biological evolution during the Ediacaran Methods employed. We undertook deep drilling in Three Gorges area in South China to obtain continuous and fresh samples without surface alteration and oxidation. 87Sr/86Sr and 88Sr/86Sr ratios of the fresh carbonate rocks were measured with multiple collector-inductively coupled plasma-mass spectrometric techniques. We discuss the surface environmental change in the Ediacaran by comparing the Sr isotope ratios with 13C/12C and 18O/16O. Result. The chemostratigraphy of 87Sr/86Sr ratios of the drilled samples displays a smooth curve and two large positive shifts in the Ediacaran. The combination of the detailed chemostratigraphies of 13C/12C, 18O/16O, and 87Sr/86Sr enable us to find connections among them and indicates that the first large positive shift of 87Sr/86Sr is slightly preceded by negative 13C/12C and positive 18O/16O excursions. The second large positive shift of 87Sr/86Sr is simultaneous with positive 13C/12C shift and clearly precedes next negative 13C/12C excursion. Considering Mn content and Fe content of carbonate rocks, which respond to redox in the ocean, the first positive shift can be explained by Gaskiers glaciation. Exposed surface of continental crust were increased by regression accompanied by Gaskiers glaciation and enhanced weathering rate by rivers increased seawater 87Sr/86Sr. The second positive shift of 87Sr/86Sr is a long-term fluctuation. We speculate enhanced weathering rate, resulting from convergence of Gondwana supercontinent, as a cause of the second positive shift of 87Sr/86Sr. Chemostratigraphy of 88Sr/86Sr also displays a smooth curve. Before Gaskiers glaciation, 88Sr/86Sr curve have a negative correlation with 87Sr/86Sr fluctuation. We interpret that this negative correlation is explained by mass-dependent fractionation. When Sr are increased in ocean (high 87Sr/86Sr), 86Sr are selectively taken in carbonate (low 88Sr

  10. Sr Isotope Analysis of Lacustrine Fossils Reveals Paleohydrological Reorganisation in the Turkana Basin Through the Holocene.

    Science.gov (United States)

    Vonhof, H.; Lubbe, J. V. D.; Joordens, J. J.; Feibel, C. S.; Junginger, A.; Garcin, Y.; Krause-Nehring, J.; Beck, C.; Johnson, T. C.

    2015-12-01

    Lake Turkana in northern Kenya is one of the largest lakes in the East African Rift System (EARS) that experienced significant climate-driven lake level variation over the Holocene. Arguably the most important feature of Holocene climate change in the EARS is the termination of the African Humid Period (AHP), that caused a ~70 meter lake level drop in Lake Turkana. The precise hydrological response to the termination of the AHP is potentially complex, because Lake Turkana lies at the cross roads of two large atmospheric convection systems; the Intertropical Convergence Zone (ITCZ) and the Congo Air Boundary (CAB). Shifting of these atmospheric systems around the end of the AHP dramatically rearranged spatial rainfall patterns in the Turkana Basin catchment, causing changes in relative runoff contributions from the different sub-catchments in the Turkana Basin. We here present a Holocene Turkana lake water Sr-isotope reconstruction, based on the analysis of well-dated lacustrine ostracods and shells. This reconstruction reveals consistently high Sr isotope values for the early Holocene, followed by a remarkable drop of Sr isotope ratios around the AHP termination. We interpret this pattern to represent a westward shift in the location of the CAB, leading to the reduction and eventual shutdown of runoff contribution from the Chew Bahir Basin to the Turkana Basin at the end of the AHP. The record demonstrates the exceptional suitability of Sr isotope data for this type of paleohydrological reconstructions. This is mainly due to the chemically conservative Sr-isotope mass balance in EARS lake systems, which is insensitive to environmental change at seasonal timescales that so often overprints the longer term climate signal in stable (oxygen and carbon) isotope records of these lakes. Furthermore, when Sr-isotope signatures of the contributing sub-catchments are known, the observed Sr isotope trends can be interpreted in terms of spatial shifts in climate driven runoff

  11. Systematic of Nuclear Ground State Properties in Sr Isotope by Covariant Density Functional Theory

    Institute of Scientific and Technical Information of China (English)

    TIAN; Yuan

    2012-01-01

    <正>The hyperfine structure and isotope shifts of Sr-isotopes, both even-even and odd-even nuclei, are studied in the covariant density functional theory (DFT) with the new parameter set DD-PC1. Pairing correlation is treated by using the Bogoliubov with a separable form of the pairing interaction. Spin-parity,

  12. Identification of Marchfeld asparagus using Sr isotope ratio measurements by MC-ICP-MS.

    Science.gov (United States)

    Swoboda, S; Brunner, M; Boulyga, S F; Galler, P; Horacek, M; Prohaska, T

    2008-01-01

    This work focuses on testing and application of Sr isotope signatures for the fast and reliable authentication and traceability of Asparagus officinalis originating from Marchfeld, Austria, using multicollector inductively coupled plasma mass spectrometry after optimised Rb/Sr separation. The major sample pool comprises freeze-dried and microwave-digested asparagus samples from Hungary and Slovakia which are compared with Austrian asparagus originating from the Marchfeld region, which is a protected geographical indication. Additional samples from Peru, The Netherlands and Germany were limited in number and allowed therefore only restricted statistical evaluation. Asparagus samples from Marchfeld were harvested within two subsequent years in order to investigate the annual variation. The results show that the Sr isotope ratio is consistent within these 2 years of investigation. Moreover, the Sr isotope ratio of total Sr in soil was found to be significantly higher than in an NH4NO3 extract, reflecting the mobile (bioavailable) phase. The isotope composition in the latter extract corresponds well to the range found in the asparagus samples in Marchfeld, even though the concentration of Sr in asparagus shows no direct correlation to the concentration of Sr in the mobile phase of the soil. The major question was whether the 'Marchfelder Spargel' can be distinguished from samples from the neighbouring countries of Hungary and Slovakia. According to our findings, they can be clearly (100%) singled out from the Hungarian samples and can be distinguished from the Slovakian asparagus samples with a probability of more than 80%. PMID:17874075

  13. Analytical procedures for determining Pb and Sr isotopic compositions in water samples by ID-TIMS

    Directory of Open Access Journals (Sweden)

    Veridiana Martins

    2008-01-01

    Full Text Available Few articles deal with lead and strontium isotopic analysis of water samples. The aim of this study was to define the chemical procedures for Pb and Sr isotopic analyses of groundwater samples from an urban sedimentary aquifer. Thirty lead and fourteen strontium isotopic analyses were performed to test different analytical procedures. Pb and Sr isotopic ratios as well as Sr concentration did not vary using different chemical procedures. However, the Pb concentrations were very dependent on the different procedures. Therefore, the choice of the best analytical procedure was based on the Pb results, which indicated a higher reproducibility from samples that had been filtered and acidified before the evaporation, had their residues totally dissolved, and were purified by ion chromatography using the Biorad® column. Our results showed no changes in Pb ratios with the storage time.

  14. Re-evaluation of interferences of doubly charged ions of heavy rare earth elements on Sr isotopic analysis using multi-collector inductively coupled plasma mass spectrometry

    International Nuclear Information System (INIS)

    We re-evaluate the interference of doubly charged heavy rare earth elements during Sr isotopic analysis using multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS). A series of mixed solutions of standard reference material SRM 987, rare earth elements, and Sr separated from rock reference materials are measured to assess the influence of isobaric interferences on the MC-ICP-MS analysis of Sr isotopes. After sample dissolution, conventional cation-exchange chromatography is employed for Sr purification of rock reference materials prior to MC-ICP-MS measurement. It has been demonstrated that if the natural abundances of Er and Yb are used to correct for doubly charged ion interferences on Sr, an overcorrection results. In contrast, the use of measured doubly charged ion ratios results in an accurate and precise correction of isobaric interference. This finding is confirmed by analytical results for several certified reference materials from mafic (basaltic) to felsic (granitic) silicate rocks. It is noteworthy that, because Er is more prone to doubly charged ion formation, it dominates over Yb doubly charged ions as an interference source. - Highlights: • We re-investigated interference of doubly charged HREE ion on Sr isotope. • Natural abundance of Er and Yb to correct the interference leads to an overcorrection. • Er is more prone to doubly charged ion formation than Yb

  15. Sr, Nd, Pb Isotope geochemistry and magma evolution of the potassic volcanic rocks, Wudalianchi, Northeast China

    Science.gov (United States)

    Junwen, W.; Guanghong, X.; Tatsumoto, M.; Basu, A.R.

    1989-01-01

    Wudalianchi volcanic rocks are the most typical Cenozoic potassic volcanic rocks in eastern China. Compositional comparisons between whole rocks and glasses of various occurrences indicate that the magma tends to become rich in silica and alkalis as a result of crystal differentiation in the course of evolution. They are unique in isotopic composition with more radiogenic Sr but less radiogenic Pb.87Sr /86 Sr is higher and143Nd/144Nd is lower than the undifferentiated global values. In comparison to continental potash volcanic rocks, Pb isotopes are apparently lower. These various threads of evidence indicate that the rocks were derived from a primary enriched mantle which had not been subjected to reworking and shows no sign of incorporation of crustal material. The correlation between Pb and Sr suggests the regional heterogeneity in the upper mantle in terms of chemical composition. ?? 1989 Institute of Geochemistry, Chinese Academy of Sciences.

  16. Pb-, Sr- and Nd-Isotopic systematics and chemical characteristics of cenozoic basalts, Eastern China

    Science.gov (United States)

    Peng, Z.C.; Zartman, R.E.; Futa, K.; Chen, D.G.

    1986-01-01

    Forty-eight Paleogene, Neogene and Quaternary basaltic rocks from northeastern and east-central China have been analyzed for major-element composition, selected trace-element contents, and Pb, Sr and Nd isotopic systematics. The study area lies entirely within the marginal Pacific tectonic domain. Proceeding east to west from the continental margin to the interior, the basalts reveal an isotopic transition in mantle source material and/or degree of crustal interaction. In the east, many of the rocks are found to merge both chemically and isotopically with those previously reported from the Japanese and Taiwan island-arc terrains. In the west, clear evidence exists for component(s) of Late Archean continental lithosphere to be present in some samples. A major crustal structure, the Tan-Lu fault, marks the approximate boundary between continental margin and interior isotopic behaviors. Although the isotopic signature of the western basalts has characteristics of lower-crustal contamination, a subcrustal lithosphere, i.e. an attached mantle keel, is probably more likely to be the major contributor of their continental "flavor". The transition from continental margin to interior is very pronounced for Pb isotopes, although Sr and Nd isotopes also combine to yield correlated patterns that deviate strikingly from the mid-ocean ridge basalt (MORB) and oceanic-island trends. The most distinctive chemical attribute of this continental lithosphere component is its diminished U Pb as reflected in the Pb isotopic composition when compared to sources of MORB, oceanic-island and island-arc volcanic rocks. Somewhat diminished Sm Nd and elevated Rb Sr, especially in comparison to the depleted asthenospheric mantle, are also apparent from the Nd- and Sr-isotopic ratios. ?? 1986.

  17. Sr Isotopic Evidence on the Spilitic Degradation of the Deccan Basalt

    Indian Academy of Sciences (India)

    K V Subbarao

    2000-03-01

    Similar Sr isotopic ratios (∼0.7055) for the tholeiite-spilite flow unit and the associated mineral phases, of Bombay (Deccan Traps) provide a direct evidence for the spilitic degradation of tholeiite. In contrast, a dramatic increase in the rare earth elements (REE) from basalt to spilite is rather puzzling as rare earths are considered to be relatively immobile. The geochemistry thus suggests that the process of spilitization is due to the reaction with a complex fluid having identical Sr-isotopic composition as that of the basaltic magma - thereby masking the details of the mixing process.

  18. Geothermal waters from the Taupo Volcanic Zone, New Zealand: Li, B and Sr isotopes characterization

    International Nuclear Information System (INIS)

    Chemical and isotopic data for 23 geothermal water samples collected in New Zealand within the Taupo Volcanic Zone (TVZ) are reported. Major and trace elements including Li, B and Sr and their isotopic compositions (δ7Li, δ11B, 87Sr/86Sr) were determined in high temperature geothermal waters collected from deep boreholes in different geothermal fields (Ohaaki, Wairakei, Mokai, Kawerau and Rotokawa geothermal systems). Lithium concentrations are high (from 4.5 to 19.9 mg/L) and Li isotopic compositions (δ7Li) are homogeneous, ranging between −0.5‰ and +1.4‰. In particular, it is noteworthy that, except for the samples from the Kawerau geothermal field having slightly higher δ7Li values (+1.4%), the other geothermal waters have a near constant δ7Li signature around a mean value of 0‰ ± 0.6 (2σ, n = 21). Boron concentrations are also high and relatively homogeneous for the geothermal samples, falling between 17.5 and 82.1 mg/L. Boron isotopic compositions (δ11B) are all negative, and display a range between −6.7‰ and −1.9‰. These B isotope compositions are in agreement with those of the Ngawha geothermal field in New Zealand. Lithium and B isotope signatures are in a good agreement with a fluid signature mainly derived from water/rock interaction involving magmatic rocks with no evidence of seawater input. On the other hand, Sr concentrations are lower and more heterogeneous and fall between 2 and 165 μg/L. The 87Sr/86Sr ratios range from 0.70549 to 0.70961. These Sr isotope compositions overlap those of the Rotorua geothermal field in New Zealand, confirming that some geothermal waters (with more radiogenic Sr) have interacted with bedrocks from the metasedimentary basement. Each of these isotope systems on their own reveals important information about particular aspects of either water source or water/rock interaction processes, but, considered together, provide a more integrated understanding of the geothermal systems from the TVZ in New

  19. Tracing of industrial aerosol sources in an urban environment using Pb, Sr, and Nd isotopes.

    Science.gov (United States)

    Geagea, Majdi Lahd; Stille, Peter; Gauthier-Lafaye, François; Millet, Maurice

    2008-02-01

    A comprehensive Pb-Sr-Nd isotope tracer study of atmospheric trace metal pollution has been performed in the urban environment of Strasbourg-Kehl. Filter dust of the principal pollutant sources (waste incinerators, thermal power plant and steel plant) and soot of car and ship exhausts have been analyzed. In addition tree barks (as biomonitors) and PM10 have been analyzed to trace and determine the distribution of the pollution in the environment. The industrial sources have highly variable epsilonNd values (-9.7 and -12.5 for incinerators and -17.5 for steel plant). Much higher epsilonNd values have been found for soot of car exhausts (-6 and -6.9). These high values make the Nd isotope system a powerful tool for the discrimination of traffic emissions but especially for the identification of diesel derived particles in the urban environment. The 206Pb/207Pb isotope ratios of gasoline are low (1.089) compared to diesel soot (1.159). The 26Pb/207Pb ratios of 1.151-1.152 for the steel plant and 1.152 for the solid waste incinerator are close to the Pb isotope ratio of diesel. The 87Sr/ 8Sr isotope ratios of the principal industrial sources vary significantly: 0.7095 for the domestic solid waste incinerator, 0.709 for the steel plant, and 0.7087 for car exhaust soot. PM10 aerosols collected in the urban center of Strasbourg show the influence of the pollutant sources at 3-7 km distance from the center. Most of the aerosols Pb isotopic compositions suggest Pb admixtures from at least three sources: a natural background and in function of the wind direction the domestic waste incinerator (S-wind) or the steel plant and the chemical waste incinerator (NE-wind). The traffic contribution can only be estimated with help of Nd isotopes. Therefore the clear identification of different pollutant sources in the urban environment is only possible by combining the three different isotope systems and is based on the fact that significant differences exist between the Pb, Sr, and

  20. Sr-O isotope systematics in the Campi Flegrei magma systems

    Science.gov (United States)

    Wörner, Gerhard; Iovine, Raffaella; Carmine Mazzeo, Fabio; D'Antonio, Massimo; Arienzo, Ilenia; Civetta, Lucia; Orsi, Giovanni

    2016-04-01

    Combined radiogenic Sr- and stable O-isotopes are a powerful tool to distinguish between (a) contamination of mantle magma sources by fluids and subducted sediment and (b) assimilation of magmas during ascent through the crust. Advance in laser fluorination mass spectrometry permits to measure small samples and single mineral grains. This allows to directly link Sr- and O-isotope measurements practically for the same sample material. Although isotopic heterogeneity remains a problem even at this level, this approach avoids problems of weathering and mineral-melt disequilibria. We analysed mineral separates (feldspar, Fe-cpx, Mg-cpx, magnetite, olivine) from 37 samples covering the stratigraphic sequence of the Campi Flegrei volcanic field: Pre-Campanian Ignimbrite (Pre CI; >39.28 ka), Campanian Ignimbrite (CI; 39.28 ka), Post Campanian Ignimbrite/Pre Neapolitan Yellow Tuff (Post CI/pre NYT; 14.90 ka), Neapolitan Yellow Tuff (NYT; 14.90 ka), and Post-Neapolitan Yellow Tuff (Post NYT; 12.8 ka-1538 A.D.) deposits. Sr isotopic compositions were determined using standard cation-exchange methods on separated hand-picked feldspar, clinopyroxene and olivine phenocrysts (~300mg) and on whole rocks, in case of not enough amount of crystals. By infrared laser fluorination was, instead, measured the oxygen isotopic composition of ~0.3 mg of hand-picked phenocrysts. Recalculating measured mineral O-isotope values to magmatic values to account for mineral-melt 18O/16O-fractionation at various SiO2-contens of the melt should provide a data set that better constrains magma isotope compositions and magma sources. Sr-isotopes span a range from 0.7069 to 0.7082 that exceed the variations in the bulk rock samples (0.7071-0.7081). However, these ranges vary significantly between eruptive periods. For example the Sr-isotope variation in the Neapolitan Yellow Tuff is only between 0.70750 and 0.70754 for minerals and whole rocks. Similarly, recalculated δ18O-melt values show a large

  1. Identification of Marchfeld asparagus using Sr isotope ratio measurements by MC-ICP-MS

    Energy Technology Data Exchange (ETDEWEB)

    Swoboda, S.; Brunner, M.; Boulyga, S.F.; Galler, P.; Prohaska, T. [University of Natural Resources and Applied Life Sciences, Department of Chemistry-VIRIS Project, Vienna (Austria); Horacek, M. [Austrian Research Centers GmbH, Seibersdorf (Austria)

    2008-01-15

    This work focuses on testing and application of Sr isotope signatures for the fast and reliable authentication and traceability of Asparagus officinalis originating from Marchfeld, Austria, using multicollector inductively coupled plasma mass spectrometry after optimised Rb/Sr separation. The major sample pool comprises freeze-dried and microwave-digested asparagus samples from Hungary and Slovakia which are compared with Austrian asparagus originating from the Marchfeld region, which is a protected geographical indication. Additional samples from Peru, the Netherlands and Germany were limited in number and allowed therefore only restricted statistical evaluation. Asparagus samples from Marchfeld were harvested within two subsequent years in order to investigate the annual variation. The results show that the Sr isotope ratio is consistent within these 2 years of investigation. Moreover, the Sr isotope ratio of total Sr in soil was found to be significantly higher than in an NH{sub 4}NO{sub 3} extract, reflecting the mobile (bioavailable) phase. The isotope composition in the latter extract corresponds well to the range found in the asparagus samples in Marchfeld, even though the concentration of Sr in asparagus shows no direct correlation to the concentration of Sr in the mobile phase of the soil. The major question was whether the 'Marchfelder Spargel' can be distinguished from samples from the neighbouring countries of Hungary and Slovakia. According to our findings, they can be clearly (100%) singled out from the Hungarian samples and can be distinguished from the Slovakian asparagus samples with a probability of more than 80%. (orig.)

  2. Pb-Sr-He isotope and trace element geochemistry of the Cape Verde Archipelago

    Science.gov (United States)

    Doucelance, Régis; Escrig, Stéphane; Moreira, Manuel; Gariépy, Clément; Kurz, Mark D.

    2003-10-01

    New lead, strontium and helium isotopic data, together with trace element concentrations, have been determined for basalts from the Cape Verde archipelago (Central Atlantic). Isotopic and chemical variations are observed at the scale of the archipelago and lead to the definition of two distinct groupings, in keeping with earlier studies. The Northern Islands (Santo Antão, São Vicente, São Nicolau and Sal) present Pb isotopic compositions below the Northern Hemisphere Reference Line (NHRL) (cf. Hart, 1984), unradiogenic Sr and relatively primitive 4He/ 3He ratios. In contrast, the Southern Islands (Fogo and Santiago) display Pb isotopes above the NHRL, moderately radiogenic Sr and MORB-like helium signatures. We propose that the dichotomy between the Northern and Southern Islands results from the presence of three isotopically distinct components in the source of the Cape Verde basalts: (1) recycled ˜1.6-Ga oceanic crust (high 206Pb/ 204Pb, low 87Sr/ 86Sr and high 4He/ 3He); (2) lower mantle material (high 3He); and (3) subcontinental lithosphere (low 206Pb/ 204Pb, high 87Sr/ 86Sr and moderately radiogenic 4He/ 3He ratios). The signature of the Northern Islands reflects mixing between recycled oceanic crust and lower mantle, to which small proportions of entrained depleted material from the local upper mantle are added. Basalts from the Southern Islands, however, require the addition of an enriched component thought to be subcontinental lithospheric material instead of depleted mantle. The subcontinental lithosphere may stem from delamination and subsequent incorporation into the Cape Verde plume, or may be remnant from delamination just before the opening of the Central Atlantic. Basalts from São Nicolau reflect the interaction with an additional component, which is identified as oceanic crustal material.

  3. Development of high through-put Sr isotope analysis for monitoring reservoir integrity for CO{sub 2} storage.

    Energy Technology Data Exchange (ETDEWEB)

    Wall, Andy; Jain, Jinesh; Stewart, Brian; Capo, Rosemary; Hakala, Alexandra J.; Hammack, Richard; Guthrie, George

    2012-01-01

    Recent innovations in multi-collector ICP-mass spectrometry (MC-ICP-MS) have allowed for rapid and precise measurements of isotope ratios in geological samples. Naturally occurring Sr isotopes has the potential for use in Monitoring, Verification, and Accounting (MVA) associated with geologic CO2 storage. Sr isotopes can be useful for: Sensitive tracking of brine migration; Determining seal rock leakage; Studying fluid/rock reactions. We have optimized separation chemistry procedures that will allow operators to prepare samples for Sr isotope analysis off site using rapid, low cost methods.

  4. Sr isotope composition of atmospheric mineral dust at Ahmedabad: provenance and seasonal variability

    International Nuclear Information System (INIS)

    Atmospheric aerosol has profound impact on global climate, biogeochemical cycles and human health. Mineral dust is one of the major components in the aerosol budget which comprise ∼ 35% of total global aerosol emission. Asian dust production is estimated to be about 800 Tg / year, which is almost half of world mineral dust emission. To improve our understanding of their sources, transport, deposition and biogeochemical impact, a comprehensive study involving chemical and isotopic composition of ambient aerosols is essential. Towards this, Sr isotopic compositions of ambient aerosol at Ahmedabad, a representative location in semi-arid region in western India, are measured since they are powerful finger print for identifying mineral dust sources and undergo insignificant alteration during transport and atmospheric processes. Ambient aerosol samples were collected using high-volume sampler with an inlet size cut off 10 μm diameter on quartz filters (8x10 inch) during 2007-2008. One fourth of the filter samples were cut and leached with 0.6N HCI to remove carbonate/labile fraction. The remaining fraction is digested with con. HF + HNO3 mixture two times and subsequently with cone. HCI + HNO3 mixture. The dried residue is taken in 0.16 N HCI and passed on Biorad AG-50w-8x resin column to separate Sr. The Sr fraction is collected and evaporated. The residue is dissolved in 0.4 NHO3 and analyzed for 87Sr/86Sr on MC-ICP-MS. Sr isotopic composition at Ahmedabad exhibits significant seasonal variation indicating pronounced temporal variability in dust sources and transport in this region. Soil derived from Decan basalt is the major dust source from western and southern region of sampling location with characteristic 87Sr/86Sr ratio 87Sr/86Sr ∼0.75. The seasonal variation in Sr isotopic composition in an annual cycle reflects the differences in source region of mineral aerosol consistent with synoptic scale wind direction over this region and demonstrates that there is

  5. Which minerals control the Nd-Hf-Sr-Pb isotopic compositions of river sediments?

    Science.gov (United States)

    Garcon, M.; Chauvel, C.; France-Lanord, C.; Limonta, M.; Garzanti, E.

    2013-12-01

    River sediments naturally sample and average large areas of eroded continental crust. They are ideal targets not only for provenance studies based on isotopic compositions, but also to establish average continental crust isotopic values. However, in large fluvial systems, mineral sorting processes significantly modify the mineralogy, and thus the geochemistry of the transported sediments. We still do not know, in any quantitative way, to what extent mineral sorting affects and fractionates the isotopic compositions of river sediments. Here, we focus on this issue and try to decipher the role of each mineral species in the bulk isotopic compositions of bedloads and suspended loads sampled at the outflow of the Ganga River that drains the Himalayan mountain range. We analyzed Nd, Hf, Sr and Pb isotopic compositions as well as trace element contents of a large number of pure mineral fractions (K-feldspar, plagioclase, muscovite, biotite, magnetite, zircon, titanite, apatite, monazite/allanite, amphibole, epidote, garnet, carbonate and clay) separated from bedload sediments. We combine these data with mineral proportions typical of the Ganga sediments to perform Monte-carlo simulations that quantify the contribution of individual mineral species to the Nd, Hf, Sr and Pb isotopic budgets of bedloads and suspended loads. We show that the isotopic systematic of river sediments is entirely buffered by very few minerals. Despite their extremely low proportions in sediments, zircon and monazite/allanite control Hf and Nd isotopes, respectively. Feldspars, epidote and carbonate buffer the Sr isotopic budget while clay, feldspars and heavy minerals dominate Pb isotopes. We also demonstrate that the observed difference in Hf, Sr and Pb isotopic compositions between bedloads and suspended loads reflects their different mineral proportions. Our findings highlight the need to be very careful about the choice of isotopic compositions measured on sediments when used as source

  6. Sr isotope evolution during chemical weathering of granites -- impact of relative weathering rates of minerals

    Institute of Scientific and Technical Information of China (English)

    MA; Yingjun

    2001-01-01

    [1]Ma, Y. J., Liu, C. Q., Geochemistry of strontium isotopes in the crust weathering system, Acta Mineralogica Sinica (in Chinese), 1998, 18(3): 350.[2]Ma, Y. J., Liu, C. Q., Using strontium isotopes to trace nutrient element circulation and hydrochemical evolution within an ecosystem, Advance in Earth Sciences (in Chinese), 1999, 14 (4): 377.[3]Brantley, S. L., Chesley, J. T., Stillings, L. L., Isotopic ratios and release rates of strontium from weathering feldspars, Geochim. Cosmochim. Acta, 1998, 62(9): 1493.[4]Blum, J. D., Erel, Y., A silicate weathering mechanism linking increases in marine 87Sr/86Sr with global glaciation, Nature, 1995, 373: 415.[5]Blum, J. D., Erel, Y., Rb-Sr isotope systematics of granitic soil chronosequence: The importance of biotite weathering, Geochim. Cosmochim. Acta, 1997, 61(15): 3193.[6]Bullen, T., Krabbenhoft, D., Kendall, C., Kinetic and mineralogic controls on the evolution of groundwater chemistry and 87Sr/86Sr in a sandy silicate aquifer, northern Wisconsin, USA, Geochim. Cosmochim. Acta, 1996, 60: 1807.[7]Bullen, T., White, A., Blum, A. et al., Chemical weathering of a soil chronosequence on granitoid alluvium: Ⅱminer-alogic and isotopic constraints on the behavior of strontium, Geochim. Cosmochim. Acta, 1997, 61: 291.[8]Blum, J. D., Erel, Y., Brown, K., 87Sr/86Sr ratios of Sierra Nevada stream waters: Implications for relative mineral weath-ering rates, Geochim. Cosmochim. Acta, 1993, 57: 5019.[9]Ma Yingjun, Trace element and strontium isotope geochemistry during chemical weathering, Ph. D. Dissertation, 1999, Institute of Geochemistry, Chinese Academy of Sciences.[10]Nesbitt, H. W., Markovics, G., Price, R. C., Chemical processes affecting alkalis and alkaline earths during continental weathering, Geochim. Cosmochim. Acta, 1980, 44: 1659.[11]Clauer, N., Strontium and argon isotopes in naturally weathered biotites, muscovites and feldspars, Chem. Geol., 1981, 31: 325.[12

  7. Derivation of Apollo 14 High-Al Basalts at Discrete Times: Rb-Sr Isotopic Constraints

    Science.gov (United States)

    Hui, H.; Neal, C. R.; Shih, C.-Y.; Nyquist, L. E.

    2012-03-01

    Four eruption episodes were identified for A-14 high-Al basalts. Rb-Sr isotopic data and ITE ratios show that their parental melt compositions of are correlated through mixing of evolved components with a relatively primitive magma ocean cumulate.

  8. Stable Isotopes of Sr and Pb as Tracers of Sources of Airborne Particulate Matter in Kyrgyzstan

    Science.gov (United States)

    ConclusionsElemental concentrations were higher at the LIDAR site compared to the Bishkek site. Also, concentrations were higher during dust than non-dust events at both sites.The Sr isotopic ratios suggest dust from another region, such as from Western China, Africa, or Middle E...

  9. Sea level and climate forcing of the Sr isotope composition of late Miocene Mediterranean marine basins

    Science.gov (United States)

    Schildgen, T. F.; Cosentino, D.; Frijia, G.; Castorina, F.; Dudas, F. Ö.; Iadanza, A.; Sampalmieri, G.; Cipollari, P.; Caruso, A.; Bowring, S. A.; Strecker, M. R.

    2014-07-01

    isotope records from marginal marine basins track the mixing between seawater and local continental runoff, potentially recording the effects of sea level, tectonic, and climate forcing in marine fossils and sediments. Our 110 new 87Sr/86Sr analyses on oyster and foraminifera samples from six late Miocene stratigraphic sections in southern Turkey, Crete, and Sicily show that 87Sr/86Sr fell below global seawater values in the basins several million years before the Messinian Salinity Crisis, coinciding with tectonic uplift and basin shallowing. 87Sr/86Sr from more centrally located basins (away from the Mediterranean coast) drop below global seawater values only during the Messinian Salinity Crisis. In addition to this general trend, 55 new 87Sr/86Sr analyses from the astronomically tuned Lower Evaporites in the central Apennines (Italy) allow us to explore the effect of glacio-eustatic sea level and precipitation changes on 87Sr/86Sr. Most variation in our data can be explained by changes in sea level, with greatest negative excursions from global seawater values occurring during relative sea level lowstands, which generally coincided with arid conditions in the Mediterranean realm. We suggest that this greater sensitivity to lowered sea level compared with higher runoff could relate to the inverse relationship between Sr concentration and river discharge. Variations in the residence time of groundwater within the karst terrain of the circum-Mediterranean region during arid and wet phases may help to explain the single (robust) occurrence of a negative excursion during a sea level highstand, but this explanation remains speculative without more detailed paleoclimatic data for the region.

  10. The use of Pb, Sr, and Hg isotopes in Great Lakes precipitation as a tool for pollution source attribution

    Energy Technology Data Exchange (ETDEWEB)

    Sherman, Laura S., E-mail: lsaylors@umich.edu [University of Michigan, Department of Earth and Environmental Sciences, 1100 N. University Ave., Ann Arbor, MI 48109 (United States); Blum, Joel D. [University of Michigan, Department of Earth and Environmental Sciences, 1100 N. University Ave., Ann Arbor, MI 48109 (United States); Dvonch, J. Timothy [University of Michigan, Air Quality Laboratory, 1415 Washington Heights, Ann Arbor, MI 48109 (United States); Gratz, Lynne E. [University of Washington-Bothell, 18115 Campus Way NE, Bothell, WA 98011 (United States); Landis, Matthew S. [U.S. EPA, Office of Research and Development, Research Triangle Park, NC 27709 (United States)

    2015-01-01

    The anthropogenic emission and subsequent deposition of heavy metals including mercury (Hg) and lead (Pb) present human health and environmental concerns. Although it is known that local and regional sources of these metals contribute to deposition in the Great Lakes region, it is difficult to trace emissions from point sources to impacted sites. Recent studies suggest that metal isotope ratios may be useful for distinguishing between and tracing source emissions. We measured Pb, strontium (Sr), and Hg isotope ratios in daily precipitation samples that were collected at seven sites across the Great Lakes region between 2003 and 2007. Lead isotope ratios ({sup 207}Pb/{sup 206}Pb = 0.8062 to 0.8554) suggest that Pb deposition was influenced by coal combustion and processing of Mississippi Valley-Type Pb ore deposits. Regional differences in Sr isotope ratios ({sup 87}Sr/{sup 86}Sr = 0.70859 to 0.71155) are likely related to coal fly ash and soil dust. Mercury isotope ratios (δ{sup 202}Hg = − 1.13 to 0.13‰) also varied among the sites, likely due to regional differences in coal isotopic composition, and fractionation occurring within industrial facilities and in the atmosphere. These data represent the first combined characterization of Pb, Sr, and Hg isotope ratios in precipitation collected across the Great Lakes region. We demonstrate the utility of multiple metal isotope ratios in parallel with traditional trace element multivariate statistical modeling to enable more complete pollution source attribution. - Highlights: • We measured Pb, Sr, and Hg isotopes in precipitation from the Great Lakes region. • Pb isotopes suggest that deposition was impacted by coal combustion and metal production. • Sr isotope ratios vary regionally, likely due to soil dust and coal fly ash. • Hg isotopes vary due to fractionation occurring within facilities and the atmosphere. • Isotope results support conclusions of previous trace element receptor modeling.

  11. The use of Pb, Sr, and Hg isotopes in Great Lakes precipitation as a tool for pollution source attribution

    International Nuclear Information System (INIS)

    The anthropogenic emission and subsequent deposition of heavy metals including mercury (Hg) and lead (Pb) present human health and environmental concerns. Although it is known that local and regional sources of these metals contribute to deposition in the Great Lakes region, it is difficult to trace emissions from point sources to impacted sites. Recent studies suggest that metal isotope ratios may be useful for distinguishing between and tracing source emissions. We measured Pb, strontium (Sr), and Hg isotope ratios in daily precipitation samples that were collected at seven sites across the Great Lakes region between 2003 and 2007. Lead isotope ratios (207Pb/206Pb = 0.8062 to 0.8554) suggest that Pb deposition was influenced by coal combustion and processing of Mississippi Valley-Type Pb ore deposits. Regional differences in Sr isotope ratios (87Sr/86Sr = 0.70859 to 0.71155) are likely related to coal fly ash and soil dust. Mercury isotope ratios (δ202Hg = − 1.13 to 0.13‰) also varied among the sites, likely due to regional differences in coal isotopic composition, and fractionation occurring within industrial facilities and in the atmosphere. These data represent the first combined characterization of Pb, Sr, and Hg isotope ratios in precipitation collected across the Great Lakes region. We demonstrate the utility of multiple metal isotope ratios in parallel with traditional trace element multivariate statistical modeling to enable more complete pollution source attribution. - Highlights: • We measured Pb, Sr, and Hg isotopes in precipitation from the Great Lakes region. • Pb isotopes suggest that deposition was impacted by coal combustion and metal production. • Sr isotope ratios vary regionally, likely due to soil dust and coal fly ash. • Hg isotopes vary due to fractionation occurring within facilities and the atmosphere. • Isotope results support conclusions of previous trace element receptor modeling

  12. Rb-Sr isotope systematics in the magmatic rocks of the Oslo Rift

    International Nuclear Information System (INIS)

    Fifty-one different units of Oslo Rift magmatic rocks have been investigated by the Rb-Sr isotope method. Isochron ages obtained for all but three of the units vary between 295 Ma and 240 Ma. The ages from the southern segment of the rift are generally older than those from the northern segment, suggesting a northward migration of the magmatic activity time. 87Sr/86Sr initial ratios obtained for rhomb-porphyry lavas, larvikites and related rocks are compatible with a moderately LIL-depleted mantle source with a Rb/Sr ratio of about 0.04. Crustal contamination in magma chambers and/or during ascent to the surface is also demonstrated for these rocks. 72 refs., 7 figs., 3 tabs

  13. Rb-Sr isotopic and geochronological studies of the granitic rocks of Dalhousie area, Himachal Pradesh

    International Nuclear Information System (INIS)

    Rb-Sr isotopic and geochronological investigations have been carried out on the granitic rocks of Dalhousie area, Himachal Pradesh. The data give an isochron age of 316 ± 11 Ma with initial ratio of 87Sr/86Sr equal to 0.7698 ± 0.0041 based on nine samples of granitic rocks of inner or eastern band. The initial Sr ratio is quite high which indicates that the granitic rocks of inner or eastern band were formed by remobilization of older sialic rocks. The thickness of outer or western band varies from 120 m to 150 m, so it is not possible to obtain the isochron age. The data of outer or western granitic band give model ages ranging from 2045 Ma to 2158 Ma where as BN-2 and BN-3 provide model ages of 1686 Ma and 1845 Ma, respectively

  14. REE characteristics and Pb, Sr and Nd isotopic compositions of steel plant emissions.

    Science.gov (United States)

    Geagea, M Lahd; Stille, P; Millet, M; Perrone, Th

    2007-02-01

    A comprehensive Pb-Sr-Nd isotope and REE tracer study of atmospheric trace metal pollution by a steel plant situated to the north of the urban communities of Strasbourg (France) and Kehl (Germany) has been performed using tree barks as biomonitors. The 206Pb/207Pb and 208Pb/207Pb isotopic ratios of the steel plant's filter dust are similar to values found in dust of waste incinerators. The 87Sr/86Sr ratio is similar to present-day ratios of Phanerozoic or Precambrian granitic rocks. The 143Nd/144Nd isotopic composition is very low and corresponds to an (Nd) value of -17.5. Such a low value is characteristic of old Precambrian granitic rocks and banded iron formations. Thus, this low (Nd) value might point to the origin of the iron necessary for the steel production. The fact, that this isotopic composition does not occur in crustal rocks of Western Central Europe makes the Nd isotope ratio a powerful tool to trace steel plants atmospheric emissions. The rare earth element (REE) distribution pattern of the steel plant's filter dust shows very specific fractionations like La and Nd enrichments which are traceable in tree barks over a distance of 4 km. The Pb, Sr and Nd isotope ratios not only enable the steel plant's emissions to be traced in a north-easterly direction, along the principal wind pathway but also enables the interference of this emission at 4 km NE from the steel plant with another atmospheric component originating from the Strasbourg Rhine harbour to be identified.

  15. Conservation of (87)Sr/(86)Sr isotopic ratios during the winemaking processes of 'Red' wines to validate their use as geographic tracer.

    Science.gov (United States)

    Marchionni, Sara; Buccianti, Antonella; Bollati, Andrea; Braschi, Eleonora; Cifelli, Francesca; Molin, Paola; Parotto, Maurizio; Mattei, Massimo; Tommasini, Simone; Conticelli, Sandro

    2016-01-01

    (87)Sr/(86)Sr has been determined in wines, musts grape juices, soils and rocks from six selected vineyards of 'Cesanese' wine area. Cesanese is a monocultivar wine from a small region characterised by different geologic substrata, a key locality to test the influence of both substratum and winemaking procedure on the (87)Sr/(86)Sr of wines. Experimental work has been performed on wines from different vintage years to check possible seasonal variations. The data reveal that (87)Sr/(86)Sr does not change through time, to validate the selection of wineries performed, and in addition no isotopic variations are observed during winemaking. Indeed, no significant isotopic variations have been observed in musts and wines. These findings reinforce the hypothesis that the isotopic signature of wines is strongly related to the bioavailable fraction of the soil rather than to its bulk. The data corroborate the possibility that Sr-isotopes of high-quality wines can be used as a reliable tool for fingerprinting wine geographic provenance.

  16. Conservation of (87)Sr/(86)Sr isotopic ratios during the winemaking processes of 'Red' wines to validate their use as geographic tracer.

    Science.gov (United States)

    Marchionni, Sara; Buccianti, Antonella; Bollati, Andrea; Braschi, Eleonora; Cifelli, Francesca; Molin, Paola; Parotto, Maurizio; Mattei, Massimo; Tommasini, Simone; Conticelli, Sandro

    2016-01-01

    (87)Sr/(86)Sr has been determined in wines, musts grape juices, soils and rocks from six selected vineyards of 'Cesanese' wine area. Cesanese is a monocultivar wine from a small region characterised by different geologic substrata, a key locality to test the influence of both substratum and winemaking procedure on the (87)Sr/(86)Sr of wines. Experimental work has been performed on wines from different vintage years to check possible seasonal variations. The data reveal that (87)Sr/(86)Sr does not change through time, to validate the selection of wineries performed, and in addition no isotopic variations are observed during winemaking. Indeed, no significant isotopic variations have been observed in musts and wines. These findings reinforce the hypothesis that the isotopic signature of wines is strongly related to the bioavailable fraction of the soil rather than to its bulk. The data corroborate the possibility that Sr-isotopes of high-quality wines can be used as a reliable tool for fingerprinting wine geographic provenance. PMID:26213038

  17. Minor-element and Sr-isotope geochemistry of tertiary stocks, Colorado mineral belt

    Science.gov (United States)

    Simmons, E.C.; Hedge, C.E.

    1978-01-01

    Rocks of the northeast portion of the Colorado mineral belt form two petrographically, chemically and geographically distinct rock suites: (1) a silica oversaturated granodiorite suite; and (2) a silica saturated, high alkali monzonite suite. Rocks of the granodiorite suite generally have Sr contents less than 1000 ppm, subparallel REE patterns and initial 87Sr/ 86Sr ratios greater than 0.707. Rocks of the monzonite suite are restricted to the northeast part of the mineral belt, where few rocks of the granodiorite suite occur, and generally have Sr contents greater than 1000 ppm, highly variable REE patterns and 87Sr/86Sr initial ratios less than 0.706. Despite forming simple, smooth trends on major element variation diagrams, trace element data for rocks of the granodiorite suite indicate that they were not derived from a single magma. These rocks were derived from magmas having similar REE patterns, but variable Rb and Sr contents, and Rb/Sr ratios. The preferred explanation for these rocks is that they were derived by partial melting of a mixed source, which yielded pyroxene granulite or pyroxenite residues. The monzonite suite is chemically and petrographically more complex than the granodiorite suite. It is subdivided here into alkalic and mafic monzonites, and quartz syenites, based on the textural relations of their ferromagnesian phases and quartz. The geochemistry of these three rock types require derivation from separate and chemically distinct magma types. The preferred explanation for the alkalic monzonites is derivation from a heterogeneous mafic source, leaving a residue dominated by garnet and clinopyroxene. Early crystallization of sphene from these magmas was responsible for the severe depletion of the REE observed in the residual magmas. The lower Sr content and higher Rb/Sr ratios of the mafic monzonites requires a plagioclase-bearing source. The Sr-isotope systematics of the majority of these rocks are interpreted to be largely primary, and not

  18. Sr, Ca, and C isotope systematic in small tropical catchments, La Selva, Costa Rica

    Science.gov (United States)

    Wiegand, B. A.; Schwendenmann, L.

    2010-12-01

    Sr, Ca, and C isotopes were analyzed to assess sources and biogeochemical processes affecting surface and groundwater composition of four small catchments located at La Selva Biological Station, Costa Rica. 87Sr/86Sr ratios were employed to quantify inputs from mineral weathering and atmospheric sources. δ13C values of dissolved organic carbon (DOC) and δ44Ca values provide information on biological processes that affect water chemistry. Sr2+ and Ca2+ concentrations of surface and groundwater show large variations due to intermixture of bedrock groundwater with local groundwater [1]. Low 87Sr/86Sr ratios suggest weathering of volcanic rocks as the primary solute source in bedrock groundwater, while atmospheric and in situ weathering contributions are predominant in local groundwater. Contributions of bedrock groundwater constitute > 60 % in the Salto, Saltito and Arboleda catchments, whereas the Taconazo catchment receives atmospheric inputs of > 95 % in addition to local weathering contributions. Surface water and groundwater wells show δ13C-DOC values between -24 ‰ and -30 ‰ due to transfer of organic carbon from the soil zone. δ44Ca values of dissolved Ca2+ in surface and groundwater are considerably fractionated from the input sources rainwater and bedrock groundwater. Light δ44Ca values are preferentially distributed in stream water and shallow groundwater horizons and contrast with heavy Ca isotopes in deeper groundwater wells. Biological processes including plant uptake and decomposition in combination with cation exchange processes in the soils may explain the fractionation of Ca isotopes. [1]Genereux et al., 2009. Water Resour. Res, 45, W08413, doi:10.1029/2008WR007630

  19. Re-Os geochronology and coupled Os-Sr isotope constraints on the Sturtian snowball Earth.

    Science.gov (United States)

    Rooney, Alan D; Macdonald, Francis A; Strauss, Justin V; Dudás, Francis Ö; Hallmann, Christian; Selby, David

    2014-01-01

    After nearly a billion years with no evidence for glaciation, ice advanced to equatorial latitudes at least twice between 717 and 635 Mya. Although the initiation mechanism of these Neoproterozoic Snowball Earth events has remained a mystery, the broad synchronicity of rifting of the supercontinent Rodinia, the emplacement of large igneous provinces at low latitude, and the onset of the Sturtian glaciation has suggested a tectonic forcing. We present unique Re-Os geochronology and high-resolution Os and Sr isotope profiles bracketing Sturtian-age glacial deposits of the Rapitan Group in northwest Canada. Coupled with existing U-Pb dates, the postglacial Re-Os date of 662.4 ± 3.9 Mya represents direct geochronological constraints for both the onset and demise of a Cryogenian glaciation from the same continental margin and suggests a 55-My duration of the Sturtian glacial epoch. The Os and Sr isotope data allow us to assess the relative weathering input of old radiogenic crust and more juvenile, mantle-derived substrate. The preglacial isotopic signals are consistent with an enhanced contribution of juvenile material to the oceans and glacial initiation through enhanced global weatherability. In contrast, postglacial strata feature radiogenic Os and Sr isotope compositions indicative of extensive glacial scouring of the continents and intense silicate weathering in a post-Snowball Earth hothouse.

  20. Rb-Sr and Sm-Nd Isotopic Studies of Lunar Green and Orange Glasses

    Science.gov (United States)

    Shih, C.-Y.; Nyquist, L. E.; Reese, Y.

    2012-01-01

    Lunar volcanic glassy beads have been considered as quenched basaltic magmas derived directly from deep lunar mantle during fire-fountaining eruptions [1]. Since these sub-mm size glassy melt droplets were cooled in a hot gaseous medium during free flight [2], they have not been subject to mineral fractionations. Thus, they represent primary magmas and are the best samples for the investigation of the lunar mantle. Previously, we presented preliminary Rb- Sr and Sm-Nd isotopic results for green and orange glassy samples from green glass clod 15426,63 and orange soil 74220,44, respectively [3]. Using these isotopic data, initial Sr-87/Sr-86 and Nd ratios for these pristine mare glass sources can be calculated from their respective crystallization ages previously determined by other age-dating techniques. These isotopic data were used to evaluate the mineralogy of the mantle sources. In this report, we analyzed additional glassy samples in order to further characterize isotopic signatures of their source regions. Also, we'll postulate a relationship between these two major mare basalt source mineralogies in the context of lunar magma ocean dynamics.

  1. Early solar system aqueous activity - Sr isotope evidence from the Orgueil CI meteorite

    Science.gov (United States)

    Macdougall, J. D.; Lugmair, G. W.; Kerridge, J. F.

    1984-01-01

    The Sr isotopic composition and Rb-87/Sr-86 ratio have been measured in carbonates and sulfate separated from the Orgueil meteorite in order to determine the time when liquid water may have acted on the parent body. Both of the studied phases probably precipitated from aqueous solution. The results show that carbonate deposition occurred contemporaneously with parent body formation or shortly after it, probably within 100 Myr. On the other hand, at least some of the calcium sulfate seems to have been formed recently.

  2. Ca, Sr and Ba stable isotopes reveal the fate of soil nutrients along a tropical climosequence

    Science.gov (United States)

    Bullen, Thomas D.; Chadwick, Oliver A.

    2016-01-01

    Nutrient biolifting is an important pedogenic process in which plant roots obtain inorganic nutrients such as phosphorus (P) and calcium (Ca) from minerals at depth and concentrate those nutrients at the surface. Here we use soil chemistry and stable isotopes of the alkaline earth elements Ca, strontium (Sr) and barium (Ba) to test the hypothesis that biolifting of P has been an important pedogenic process across a soil climosequence developed on volcanic deposits at Kohala Mountain, Hawaii. The geochemical linkage between these elements is revealed as generally positive site-specific relationships in soil mass gains and losses, particularly for P, Ba and Ca, using the ratio of immobile elements titanium and niobium (Ti/Nb) to link individual soil samples to a restricted compositional range of the chemically and isotopically diverse volcanic parent materials. At sites where P is enriched in surface soils relative to abundances in deeper soils, the isotope compositions of exchangeable Ca, Sr and Ba in the shallowest soil horizons (materials and trend toward those of plants growing on fresh volcanic deposits. In contrast the isotope composition of exchangeable Ba in deeper soil horizons (> 10 cm depth) at those sites is consistently heavier than the volcanic parent materials. The isotope compositions of exchangeable Ca and Sr trend toward heavier compositions with depth more gradually, reflecting increasing leakiness from these soils in the order Ba recycling flux returned to the surface as litterfall. This observation implicates an uptake flux from an additional source which we attribute to biolifting. We view the heavy exchangeable Ba relative to soil parent values in deeper soils at sites where P is enriched in surface soils, and indeed at all but the wettest site across the climosequence, to represent the complement of an isotopically light Ba fraction removed from these soils by plant roots consistent with the biolifting hypothesis. We further suggest that

  3. The geographic distribution of Sr isotopes from surface waters and soil extracts over the island of Bornholm (Denmark) – A base for provenance studies in archaeology and agriculture

    DEFF Research Database (Denmark)

    Frei, Robert; Frei, Karin Margarita

    2013-01-01

    In this paper we report the Sr isotope signatures, and Sr, Al and Na concentrations of 30 surface waters (lakes/ponds and rivers/creeks) and 19 soil sample extracts from the island of Bornholm (Denmark) and present a categorized 87Sr/86Sr value distribution map that may serve as a base for proven......In this paper we report the Sr isotope signatures, and Sr, Al and Na concentrations of 30 surface waters (lakes/ponds and rivers/creeks) and 19 soil sample extracts from the island of Bornholm (Denmark) and present a categorized 87Sr/86Sr value distribution map that may serve as a base...... for provenance studies, including archaeological migration and authenticity proof for particular food products. The Sr isotopic compositions of surface waters range from 87Sr/86Sr = 0.7097–0.7281 (average 0.7175 ± 0.0049; 1σ), whereas 0.1 M HNO3, 0.05 M HNO3, and 0.01 M CaCl2 soil extracts range from 87Sr/86Sr...... Sr isotope composition vs. Sr, Na and Al concentration relationships of soil extracts imply that lowering of the isotopic composition of leachable Sr on Bornholm results as a consequence of significant admixture to this fraction of Sr deposited as marine salts (aerosols), and that rainwater only has...

  4. Sr and Nd isotopes of suspended sediments from rivers of the Amazon basin

    Science.gov (United States)

    Hatting, Karina; Santos, Roberto V.; Sondag, Francis

    2014-05-01

    The Rb-Sr and Sm-Nd isotopic systems are important tools to constrain the provenance of sediment load in river systems. This study presents the isotopic composition of Sr and Nd isotopes and major and minor elements in suspended sediments from the Marañón-Solimões, Amazonas and Beni-Madeira rivers. The data were used to constrain the source region of the sediments and to better understand the main seasonal and spatial transport processes within the basin based on the variations of the chemical and isotopic signals. They also allow establishing a relationship between sediment concentrations and flow rate values. The study presents data collected during a hydrological year between 2009 and 2010. The Marañón-Solimões River presents low Sr isotopic values (0.7090-0.7186), broad EpslonNd(0) range (-15.17 to -8.09) and Nd model (TDM) ages varying from 0.99 to 1.81 Ga. Sources of sediments to the Marañón-Solimões River include recent volcanic rocks in northern Peru and Ecuador, as well as rocks with long crustal residence time and carbonates from the Marañón Basin, Peru. The Beni-Madeira River has more radiogenic Sr isotope values (0.7255-0.7403), more negative EpslonNd(0) values (-20.46 to -10.47), and older Nd isotope model ages (from 1.40 to 2.35 Ga) when compared to the Marañón-Solimões River. These isotope data were related to the erosion of Paleozoic and Cenozoic foreland basins that are filled with Precambrian sediments derived from the Amazonian Craton. These basins are located in Bolivian Subandina Zone. The Amazon River presents intermediate isotopic values when compared to those found in the Marañón-Solimões and Beni-Madeira rivers. Its Sr isotope ratios range between 0.7193 and 0.7290, and its EpslonNd(0) values varies between -11.09 and -9.51. The Nd isotope model ages of the suspended sediments vary between 1.28 and 1.77 Ga. Concentrations of soluble and insoluble elements indicate a more intense weathering activity in sediments of the Beni

  5. Sr isotopic chemostratigraphy of Precambrian carbonate rocks in the Amderma Rise, Pai-Khoi Ridge

    Science.gov (United States)

    Kuznetsov, A. B.; Starikova, E. V.; Maslov, A. V.; Konstantinova, G. V.

    2016-08-01

    The Sr and C isotopic compositions of Precambrian carbonate rocks are determined for Amderma Rise, in the northeastern margin of Pai-Khoi Ridge. Based on the Sr isotopic chemostratigraphy, it is established for the first time that the Amderma Formation is referred to the Early Vendian, while the Morozovsk Formation is Late Riphean in age. This conclusion along with detailed mapping proves that the Precambrian "section" of the Amderma Rise is a series of tectonic plates combined in a nonchronostratigraphic order. Volcanic and sedimentary rocks of the Morozovsk and Sokolninsk formations make up the allochthon proper, while carbonate rocks of the Amderma Formation make up the para-autochthon. The high values of δ13C (up to +9.5‰) identified in limestones of both formations suggest a considerable distance of the Pai-Khoi paleobasin from the passive margin of the Baltic Region upon facies similarity to the Laurentia active margins.

  6. Provenance of sedimentary kaolin deposits in Egypt: Evidences from the Pb, Sr and Nd isotopes

    Science.gov (United States)

    Baioumy, Hassan

    2014-12-01

    This work reports, for the first time, the Pb, Sr and Nd isotopes of the clay fractions (kaolin deposits in Egypt of different ages (Carboniferous and lower Cretaceous), localities (Sinai, Red Sea and Aswan), lithologies (flint and plastic) and clay minerals composition (pure kaolinite and mixture of kaolinite, illite and chlorite) to determine their source area compositions and examine the effect of provenance on their isotopic compositions. Measured (present day) and age-corrected Pb isotopes data (100 and 300 My for the Cretaceous and Carboniferous deposits, respectively) are more or less homogeneous in all deposits regardless of their ages, localities, and compositions. This, therefore, suggests that the Pb isotopes cannot be used as a tracer for source area compositions of these kaolin deposits. On the other hand, the studied kaolin deposits show variations in their measured and age-corrected Sr and Nd isotopes regarding to their ages and compositions. The Carboniferous illite-rich kaolin deposits in the Khaboba and Hasbar areas, Sinai have higher measured and age-corrected 87Sr/86Sr ratios (average of 0.715742 and 0.711156 for measured and age-corrected, respectively) compared to the non-illitic Carboniferous deposit at Abu Natash area (average of 0.70772 and 0.70769 for measured and age-corrected, respectively) and the lower Cretaceous deposits in all areas (average of 0.70827 and 0.70821 for measured and age-corrected, respectively). The Carboniferous kaolin deposits in the Khaboba and Hasbar areas also have lower 143Nd/144Nd ratios (average of 0.51206 and 0.51180 for measured and age-corrected, respectively) compared to the Carboniferous Abu Natash deposit (average of 0.51253 and 0.51231 for measured and age-corrected, respectively) as well as the lower Cretaceous deposits in all areas (average of 0.51248 and 0.51239 for measured and age-corrected, respectively). Initial εNd values are negative in the Carboniferous kaolin deposits in the Khaboba and

  7. Musa's granite and Rio Maria's granodiorite Rb/Sr isotopic ages and geochemistry

    International Nuclear Information System (INIS)

    The Musa Granite and the Rio Maria Granodiorite are located at the eastern margin of the Amazonian craton, in the Rio Maria region, where a typical granite-greenstone terrain is characterized. Rb-Sr dating of six samples from different facies of Rio Maria Granodiorite furnished an age of 2564 ± 68 Ma with initial 87Sr/86Sr radio (IR) of 0.70288 ± 0.00092 (whole rock isochron; 1 ο error; MSWD = 2.26). Thirteen samples from the three facies of Musa Granite (monzogranites, syenogranites and intermediate to felsic hypabyssal rocks) gave Rb-Sr whole rock isochron with an age of 1692 ± 11 Ma and IR of 0.70777 ± 0.00023 (1 ο error, MSWD = 1.89). A preliminary attempt to individualize geochronologically the three facies was done resulting different ages and IRs. There is a coincidence between these ages and the emplacement sequence of these facies of the pluton. The actual meaning of the Rio Maria Granodiorite Rb-Sr age is still uncertain. It could be related to the end of the magmatic crystallization of the batholith as well as to the metamorphic-mylonitic event that affect it. Considering that the Jamon and Musa Granites are petrologically similar that they occur in the same area, it is interesting to note that latter is apparently a little older than the former. The IRs obtained for the two plutons are also not coincident. The isotopic Rb-Sr available data show that the exposed rocks of the Rio Maria Granodiorite have not been able to generate magmas with the compositions of the monzongranitic and the hypabyssal facies of the Musa pluton. On the other hand, rocks isotopically similar to the Rio Maria Granodiorite would theorically be able to generate the Jamon and a magma with the characteristics of the syenogranitic facies of the Musa pluton. (author)

  8. Rb-Sr Isotopic Systematics of Felsic Igneous Rocks, Wichita Mountains, Oklahoma

    Science.gov (United States)

    Min, K.; Gilbert, M. C.

    2001-12-01

    Recently determined Rb-Sr isotopic characteristics of twelve of the recognized felsic units of the Cambrian Southern Oklahoma Aulacogen, which crop out in the Wichita Mountains of the southwestern Oklahoma, give some clues to the petrogenesis of these felsic units. 1) Plots of 87Rb/86Sr vs. 87Sr/86Sr form subsets yielding dates of 516 Ma and 522 Ma, discrepancies of about 10 to 20 Ma from the U-Pb zircon age for the Mount Scott Granite of 534 Ma, probably attributable to a systematic loss of radiogenic 87Sr for these units. 2) The Mount Scott Granite and related units (n=7) including Medicine Park Granite and Saddle Mountain Granite give a probable pseudoisochron of 516\\pm4{}Ma and an initial 87Sr/86Sr of 0.7045\\pm4{}, indicating derivation from a primitive mantle source with little crustal contamination. 3) A well-regressed line of 522\\pm2{} Ma with an initial 87Sr/86Sr of 0.7059\\pm7{} is shown by the Long Mountain Granite (n=3), one of the finer-grained western granites, and the Fort Sill Section of the Carlton Rhyolite (n=2) in the eastern Wichitas, which indicates that both were possibly derived contemporaneously from a mixed crustal-mantle source. 4) The Lugert Granite of the western Wichitas has variable and relatively high 87Sr/86Sr initials at 516 Ma probably indicating heterogeneous crustal sources. Interpretation of these data can be made with the following scenario: The earliest known felsic unit is the Carlton Rhyolite, Fort Sill Section. This must have been generated mostly from crustal melting around large mafic plutons in the mid- to lower crust. Crustal melting around the mafic plutons continued to generate liquids rising to the emplacement position, e.g., Long Mountain Granite. Following this, the host magma for the Mount Scott set of units originated dominantly by fractional crystallization from the mafic plutons. Subsequently, additional mafic magma must have moved into the lower- to mid-crust, at some other stratigraphic level, melting a

  9. Sr and Nd Isotopic and Geochemical Analysis of the Vanda Dike Swarm, Antarctica

    Science.gov (United States)

    Bray, B.; Harpp, K. S.; Geist, D.; Garcia, M. O.; Swarr, G. J.; Garman, K. A.; Buck, S. A.; Parcheta, C. E.; Matulaitis, I.

    2009-12-01

    The Vanda dike swarm, in the Dry Valleys of Antarctica, crosscuts synorogenic Cambro-Ordovician granitoid plutons produced during the Ross Orogeny, circa 500 Ma. The emplacement of the dikes broadly coincides with the transition between the cessation of subduction and the onset of extensional magmatism. Recent fieldwork included field documentation of over 600 dikes, with subsequent whole rock major and trace element analysis and Sr and Nd isotopic analyses of a representative subset. Although originally characterized as being compositionally bimodal, the compositions of the dikes range continuously from 48% to 78% SiO2. New radiogenic isotopic data from 24 samples exhibit a surprisingly wide range of ɛNd and 87Sr/86Sri values; the bulk of the samples have an age-corrected ɛNd from -12.7 to -3.0, however a subset of four of the dikes (both mafic and felsic) have ɛNd values ranging from +2.1 to 8.0. The 87Sr/86Sri ratios vary from 0.7085 to 0.7118. Notably, there is significant overlap between the isotopic signatures of the mafic and felsic rocks and no strong correlation between ɛNd and 87Sr/86Sri. Likewise, there is no correlation between either isotopic ratio and SiO2. These variations indicate that the Vanda dikes may be derived from compositionally heterogeneous sources. Additionally, Nd model ages (τDM) of the felsic dikes yield an average of ~900 Ma, suggesting derivation from a Neoproterozoic crustal source. The Vanda dike samples’ 87Sr/86Sri overlap with the high end of the range defined by the youngest plutons in the region emplaced during the Ross Orogeny (adakitic DV1b, monzonitic DV2; Cox et al., 2000). Similarly, ɛNd values of the Vanda samples most closely resemble those of the DV1b and DV2 plutons, but also extend to significantly more negative and more positive values. None of the isotopic signatures of the dikes are similar to those of the older, orogenic granites in the region (DV1a), which have lower 87Sr/86Sri averages than both the

  10. Deciphering fluid sources of hydrothermal systems: A combined Sr- and S-isotope study on barite (Schwarzwald, SW Germany)

    Science.gov (United States)

    Staude, S.; Gob, S.; Pfaff, K.; Strobele, F.; Premo, W.R.; Markl, G.

    2011-01-01

    Primary and secondary barites from hydrothermal mineralizations in SW Germany were investigated, for the first time, by a combination of strontium (Sr) isotope systematics (87Sr/86Sr), Sr contents and δ34S values to distinguish fluid sources and precipitation mechanisms responsible for their formation. Barite of Permian age derived its Sr solely from crystalline basement rocks, whereas all younger barite also incorporate Sr from formation waters of the overlying sediments. In fact, most of the Sr in younger barite is leached from Lower and Middle Triassic sediments. In contrast, most of the sulfur (S) of Permian, Jurassic and northern Schwarzwald Miocene barite originated from basement rocks. The S source of Upper Rhinegraben (URG)-related Paleogene barite differs depending on geographic position: for veins of the southern URG, it is the Oligocene evaporitic sequence, while central URG mineralizations derived its S from Middle Triassic evaporites. Using Sr isotopes of barite of known age combined with estimates on the Sr contents and Sr isotopic ratios of the fluids' source rocks, we were able to quantify mixing ratios of basement-derived fluids and sedimentary formation waters for the first time. These calculations show that Jurassic barite formed by mixing of 75–95% ascending basement-derived fluids with 5–25% sedimentary formation water, but that only 20–55% of the Sr was brought by the basement-derived fluid to the depositional site. Miocene barite formed by mixing of an ascending basement-derived brine (60–70%) with 30–40% sedimentary formation waters. In this case, only 8–15% of the Sr was derived from the deep brine. This fluid-mixing calculation is an example for deposits in which the fluid source is known. This method applied to a greater number of deposits formed at different times and in various geological settings may shed light on more general causes of fluid movement in the Earth's crust and on the formation of hydrothermal ore deposits.

  11. Extreme heterogeneity in Sr isotope systematic in the Himalayan leucogranites: A possible mechanism of partial melting based on thermal modeling

    Indian Academy of Sciences (India)

    Dilip K Mukhopadhyay

    2001-06-01

    The small leucogranite plutons occurring in linear belts in the Higher Himalayas have formed due to post-collision partial melting within the Himalayan crust. Several studies have documented that the Sr isotopic ratios in the granite bodies show chaotic variation and meaningful Rb-Sr isochron ages are difficult, if not impossible, to obtain. In tectonically overthickened crust, the depth-temperature profile (geotherm) remains strongly transient for the first tens of millions of years. It is proposed here that the intersecting relations between the transient geotherms and activity-dependent solidus/melting curves may generate small pods of magma at di erent depths and at di erent times. Each of these pods will have its unique Sr isotopic ratios. Coalescence of these small pods of magma without any e ective homogenization due to deformation-induced fast segregation, ascent and emplacement may lead to pluton-wide extreme heterogeneity in Sr isotopic ratios.

  12. U-Sr isotopic speedometer: Fluid flow and chemical weatheringrates inaquifers

    Energy Technology Data Exchange (ETDEWEB)

    Maher, Kate; DePaolo, Donald J.; Christensen, John N.

    2005-12-27

    Both chemical weathering rates and fluid flow are difficultto measure in natural systems. However, these parameters are critical forunderstanding the hydrochemical evolution of aquifers, predicting thefate and transport of contaminants, and for water resources/water qualityconsiderations. 87Sr/86Sr and (234U/238U) activity ratios are sensitiveindicators of water-rock interaction, and thus provide a means ofquantifying both flow and reactivity. The 87Sr/86Sr values in groundwaters are controlled by the ratio of the dissolution rate to the flowrate. Similarly, the (234U/238U) ratio of natural ground waters is abalance between the flow rate and the dissolution of solids, andalpha-recoil loss of 234U from the solids. By coupling these two isotopesystems it is possible to constrain both the long-term (ca. 100's to1000's of years) flow rate and bulk dissolution rate along the flow path.Previous estimates of the ratio of the dissolution rate to theinfiltration flux from Sr isotopes (87Sr/86Sr) are combined with a modelfor (234U/238U) to constrain the infiltration flux and dissolution ratefor a 70-m deep vadose zone core from Hanford, Washington. The coupledmodel for both (234U/238U) ratios and the 87Sr/86Sr data suggests aninfiltration flux of 5+-2 mm/yr, and bulk silicate dissolution ratesbetween 10-15.7 and 10-16.5 mol/m2/s. The process of alpha-recoilenrichment, while primarily responsible for the observed variation in(234U/238U) of natural systems, is difficult to quantify. However, therate of this process in natural systems affects the interpretation ofmost U-series data. Models for quantifying the alpha-recoil loss fractionbased on geometric predictions, surface area constraints, and chemicalmethods are also presented. The agreement between the chemical andtheoretical methods, such as direct measurement of (234U/238U) of thesmall grain size fraction and geometric calculations for that sizefraction, is quite good.

  13. Precision frequency measurement of 1S0–3P1 intercombination lines of Sr isotopes

    International Nuclear Information System (INIS)

    We report on frequency measurement of the intercombination (5s2)1S0–(5s5p)3P1 transition of the four natural isotopes of strontium, including 88Sr (82.58%), 87Sr (7.0%), 86Sr (9.86%), and 84Sr (0.56%). A narrow-linewidth laser that is locked to an ultra-low expansion (ULE) optical cavity with a finesse of 12000 is evaluated at a linewidth of 200 Hz with a fractional frequency drift of 2.8×10−13 at an integration time of 1 s. The fluorescence collector and detector are specially designed, based on a thermal atomic beam. Using a double-pass acousto-optic modulator (AOM) combined with a fiber and laser power stabilization configuration to detune the laser frequency enables high signal-to-noise ratios and precision saturated spectra to be obtained for the six transition lines, which allows us to determine the transition frequency precisely. The optical frequency is measured using an optical frequency synthesizer referenced to an H maser. Both the statistical values and the final values, including the corrections and uncertainties, are derived for a comparison with the values given in other works. (paper)

  14. Palaeoenvironmental Changes of the Ancient Nihewan Lake Area—Sr Isotope Evidence from Xiaodukou Foraminifera

    Institute of Scientific and Technical Information of China (English)

    王世杰

    1996-01-01

    By using the improved trace(50μg) Sr isotope analytical method the 87Sr/86Sr ratios of Xiaodukou foraminifera fossils were measured,giving a range of 0.71105-0.71274,apparently higher than the value of contemporaneous seawater(0.709087-0.709147)and also slightly higher than the average value of modern Yellow River(0.7111),demonstrating that the contemporaneous environment where Xiaodukou foraminifera inhabited was an inland lake.Detailed analyses of △ Sr values showed that there occurred an event responsible for environmental changes in the ancient Nihewan Lake area during the time(about 1.0Ma ago)when Xiaodukou foraminifera appeared.Because of strong evaporation the salinity of the lake would increase and a regional salt-water of brackish-water lacustrine environment would be produced,thus providing a suitable and inhabitable environment for foraminiferae.It is concluded that Xiaodukou foraminiferal fossil assemblaes belong to non-marine foraminiferal species.

  15. Determination of Sr and Ca sources in small tropical catchments (La Selva, Costa Rica) - A comparison of Sr and Ca isotopes

    Science.gov (United States)

    Wiegand, B. A.; Schwendenmann, L.

    2013-04-01

    SummaryA comparative study of Sr and Ca isotopes was conducted to assess solute sources and effects of biogeochemical processes on surface water and groundwater in four small tropical catchments located at La Selva Biological Station, Costa Rica. Variable concentrations of dissolved Sr2+ and Ca2+ in the catchments are related to mixing of waters from different origin. Three catchments are influenced by high-solute bedrock groundwater, while another catchment is primarily supplied by local recharge. 87Sr/86Sr ratios were employed to discriminate contributions from mineral weathering and atmospheric sources. Solutes in bedrock groundwater have a predominant geogenic origin, whereas local recharge is characterized by low-solute inputs from rainwater and minor in situ weathering releases from nutrient-depleted soils. Bedrock groundwater contributes more than 60% of dissolved Sr2+ to surface discharge in the Salto, Saltito, and Arboleda catchments, whereas the Taconazo catchment receives more than 95% of dissolved Sr2+ from rainwater. δ44/40Ca values of dissolved Ca2+ vary greatly in the catchments, mainly as a result of heterogeneous Ca isotope compositions of the contributing sources. Based on differences in δ44/40Ca values, two distinct bedrock groundwaters discharging at the Salto and the Arboleda catchments are suggested. Effects of biological processes in the plant-soil system on solute generation in the catchments are indicated by variable Ca/Sr ratios. However, these effects cannot clearly be assessed by Ca isotopes due to the strong heterogeneity of δ44/40Ca values of Ca2+ sources and high Ca2+ concentrations in bedrock groundwater.

  16. Geochemistry and Sr, Nd isotopic composition of the Hronic Upper Paleozoic basic rocks (Western Carpathians, Slovakia

    Directory of Open Access Journals (Sweden)

    Vozár Jozef

    2015-02-01

    Full Text Available The paper presents new major and trace element and first Sr-Nd isotope data from selected lavas among the Permian basaltic andesite and basalts of the Hronicum Unit and the dolerite dykes cutting mainly the Pennsylvanian strata. The basic rocks are characterized by small to moderate mg# numbers (30 to 54 and high SiO2 contents (51-57 wt. %. Low values of TiO2 (1.07-1.76 wt. % span the low-Ti basalts. Ti/Y ratios in the dolerite dykes as well as the basaltic andesite and basalt of the 1st eruption phase are close to the recommended boundary 500 between high-Ti and low-Ti basalts. Ti/Y value from the 2nd eruption phase basalt is higher and inclined to the high-Ti basalts. In spite of this fact, in all studied Hronicum basic rocks Fe2O3* is lower than 12 wt. % and Nb/La ratios (0.3-0.6 are low, which is more characteristic of low-Ti basalts. The basic rocks are characterized by Nb/La ratios (0.56 to 0.33, and negative correlations between Nb/La and SiO2, which point to crustal assimilation and fraction crystallization. The intercept for Sr evolution lines of the 1st intrusive phase basalt is closest to the expected extrusions age (about 290 Ma with an initial 87Sr/86Sr ratio of about 0.7054. Small differences in calculated values ISr document a partial Sr isotopic heterogeneity source (0.70435-0.70566, or possible contamination of the original magma by crustal material. For Nd analyses of the three samples, the calculated values εCHUR (285 Ma are positive (from 1.75 to 3.97 for all samples with only subtle variation. Chemical and isotopic data permit us to assume that the parental magma for the Hronicum basic rocks was generated from an enriched heterogeneous source in the subcontinental lithospheric mantle.

  17. Sr isotope stratigraphy and lithogenic grain-size distributions of the Pleistocene Turkana Basin, Kenya

    Science.gov (United States)

    Lubbe, J. V. D.; Sier, M.; Feibel, C. S.; Beck, C.; Dupont-Nivet, G.; Vonhof, H.; Joordens, J. J.; Cohen, A.; Prins, M. A.; Olago, D.

    2015-12-01

    The Pleistocene sedimentary infillings of the Turkana basin, a hotspot for early human evolution, document both human evolutionary and climatic events between 2.1-1.4 Ma. During this time interval, several early Homo species inhabited the vicinity of the Lorenyang paleo-lake, which was mainly fed by the Omo River, draining the Ethiopian Highlands. Paleo-Omo discharge could be expected to be modulated by changes in orbital eccentricity, causing wet-dry climate variability at ~20 kyr timescales, superimposed upon a long-term transition to drier conditions. To reconstruct climate and environmental changes during this key period of human evolution, we obtained high-resolution records of strontium (Sr) isotope ratios in lacustrine fossils as well as lithogenic grain-size distributions. High resolution sampling of sediment sequences containing abundant lacustrine fossils was carried out at outcrops situated to the east and the west of the lake. The sequences can be stratigraphically linked by several volcanic tuff layers, as well as paleomagnetic data. The Turkana basin is a half-graben and, as a consequence, the lacustrine sediment sequences along the western margin are relatively more continuous and deposited in a relatively deeper part of the lake, when compared to sequences at the eastern margin, where the paleo-Omo delta was situated. The outcrops to the west of Lake Turkana are situated in close proximity to core WTK13-1A, which was retrieved for the Hominin Sites and Paleolakes Drilling Project (HSDPD), and span approximately the same stratigraphic interval. In this study, we successfully linked the stratigraphies of the sediment core and the outcrops, the latter of which were logged in great detail in the field. In addition, time-synchronous Sr isotope records from both sides of Lake Lorenyang display similar trends in Sr isotope stratigraphy, thereby confirming the lateral correlations. However, large differences in grain-size distribution and accumulation of

  18. Petrochemistry and Rb-Sr isotopic study of bandal granites, district Kulu, Himachal Pradesh

    International Nuclear Information System (INIS)

    Bandal granites which form the subject matter of the present study occur as a concordant body of batholithic size and cover an area of about 500 sq. km. consider these granites to be the result of granitization of arkose and pelitie rocks. Whereas treats them as intrusive into the Banjar Formation, recognized two components i.e. foliated and non-foliated which made the Bandal pluton the latter is intrusive into the former. This gave an isochron age of 1220±100 Ma for the foliated granite. This paper presents the results of a petrochemical and Rb-Sr isotopic studies of these granites with a view to understand their petrogenesis

  19. Reconstructing conditions during dolomite formation on a Carnian coastal sabkha/alluvial plain using 87Sr/86Sr isotopes - Travenanzes Formation, northern Italy

    Science.gov (United States)

    Rieder, Maximilian; Wegner, Wencke; Horschinegg, Monika; Preto, Nereo; Breda, Anna; Klötzli, Urs; Peckmann, Jörn; Meister, Patrick

    2016-04-01

    The study of large amounts of dolomite that formed in the Triassic Tethyan realm is hampered by late diagenetic or hydrothermal overprint. These dolomites are difficult to link to past environmental and early diagenetic conditions, and their correlation to models for dolomite formation in modern environments is problematic. Preto et al. (2015) suggested, based on evidence from nano-scale structure analysis by transmission electron microscopy and petrographic observations, that dolomites in the Carnian Travenanzes Formation of the Southern Alps (Dolomites area) represent a preserved primary phase. The Travenanzes Formation was deposited in an extended alluvial plain or coastal sabkha environment subject to a semi-arid climate. Beds and nodules of nearly stoichiometric dolomite are embedded in large amounts of clay, which shielded early formed dolomite from diagenetic fluids. This finding of penecontemporaneous dolomite provides an ideal model case for reconstructing past environmental conditions at the time of dolomite precipitation. While Preto et al. (2015) argued that dolomite formation was mediated by extracellular polymeric substances produced by sulphate-reducing bacteria, it remains unclear whether precipitation occurred from evaporating seawater or mainly from brine derived from evaporating continental groundwater. Both cases exist in modern environments of dolomite formation. In the coastal sabkhas of Abu Dhabi and Qatar, dolomite precipitates from concentrated brine derived from seawater, either through seepage and reflux or through evaporative pumping (the sabkha model). In the coastal ephemeral lakes of the Coorong Lagoon system (South Australia) dolomite precipitation occurs from evaporating groundwater. The goal of this study is to distinguish marine from continental influence during formation of Carnian dolomite using 87Sr/86Sr isotope ratios. Sr isotopes could reveal different origins of ionic solutions for dolomite precipitation, which is not

  20. Sr and Pb isotopic geochemistry of feldspars and implications for the growth of megacrysts in plutonic settings.

    Science.gov (United States)

    Munnikhuis, J.; Glazner, A. F.; Coleman, D. S.; Mills, R. D.

    2015-12-01

    Why megacrystic textures develop in silicic igneous rocks is still unknown. One hypothesis is that these crystals nucleate early in a magma chamber with a high liquid content. A supportive observation of this hypothesis is areas in plutons with high concentrations of megacrysts suggesting flow sorting. Another group of hypotheses suggest megacrystic textures form during protracted late-stage coarsening in a low-melt, interlocked matrix due to either thermal oscillations from incremental pluton emplacement, or Ostwald ripening. Isotopic analyses of large, euhedral K-feldspar megacrysts from the Cretaceous intrusive suites of the Sierra Nevada batholith (SNB) provide new insight into their origin. Megacrysts from the SNB reach the decimeter scale, are Or rich (85-90%), are perthitic, and host mineral inclusions of nearly all phases in the host rock. In-situ micro-drilling of transects, from core to rim, of the alkali feldspars provides material for Sr and Pb isotopic analyses by thermal ionization mass spectrometry (TIMS). Preliminary 87Sr/86Sr(i) isotopic data from samples from the Cathedral Peak Granodiorite, of the Tuolumne Intrusive Suite range from 0.706337 to 0.706452 (~1.6ɛSr) near the cores, whereas a sawtooth pattern with larger variability, 0.706179 to 0.706533 (~5ɛSr), occurs nears the rims. We interpret these preliminary data to indicate that the late portion of growth (i.e. crystal rim) was dominated by either cannibalism of small K-feldspar crystals with isotopic variability, or by addition of isotopically diverse late components to the magma. By comparing the Sr and Pb isotopic stratigraphy of megacrysts from a variety of rock matrices and different granitoids in the SNB isotopic trends can be evaluated to determine if crystals sizes are dependent on disequilibrium processes or grow at a steady state.

  1. Sr ISOTOPIC EVIDENCE FOR STUDYING THE SALINIZATION OF SOILS: AN EXAMPLE FROM THE SAN VITALE PINEWOOD (RAVENNA

    Directory of Open Access Journals (Sweden)

    Umberto Masi

    2009-12-01

    Full Text Available In the frame of a multidisciplinary project of research on the San Vitale Pinewood ecosystem, north of Ravenna, the Sr isotope study of a soil profile developed on an old coastal dune aiming at detecting the effect of salinization is presented. The Sr isotope ratios of the bulk soil samples decreased significantly from upper (0.717 to lower (0.712 horizons because of the abundant marine salts deposited by the brackish water present in the deep soil. While the main source of Sr in the upper horizons is the silicates, especially the feldspaths contained in the old dune sediments; in contrast, Sr in the lower horizons is significantly also of evaporitic origin (0.707-0.709. This latter is dominantly the strontium bio-available to the plants.

  2. Sr Isotope Constraints on the Age and Source of Ore—Forming Materials of Gold Deposits,Southwestern Hunan

    Institute of Scientific and Technical Information of China (English)

    彭建堂; 戴塔根; 等

    2000-01-01

    We have measured Rb and Sr concentrations in fluid inclusions of quartz in gold deposits,southwestern Hunan,The Rb-Sr isochron ages of 435±9Ma and 412±33Ma are respectively determined,revealing that gold mineralization in this area took place in the Caledonian period rather than in the Wuling-Xuefeng period as traditionalyy considered.Sr isotope geochemistry of the hydrothermal fluid indicates that the ore-forming materials are of crust origin,derived largely from the ore-hositng strata rather than from the basic dikes.

  3. Sr-Nd isotopes constrain on the deposit history of the basins in the Gulf of Mexico

    Science.gov (United States)

    Li, Y.; Jiang, S.

    2015-12-01

    The Brazos-Trinity Basin IV and Ursa Basin are situated on the northern slope of the Gulf of Mexico. The Ursa basin lies in the center of late Pleistocene Mississippi River deposition, received the sediment deposition during Marine Isotope Stage (MIS) 2- 4. The Brazos-Trinity Basin IV belongs to a part of the Brazos-Trinity fan, it recorded the turbidite deposition and hemiplegic deposition during MIS1- 5. The Sr and Nd isotopic composition of the detrital composition of the sediment in both basins indicates the change of the sediment provenance during the basin-filled process. In the Ursa basin, The difference of 87Sr/86Sr ratio and ɛNd of the detrital component between MIS1,2 (87Sr/86Sr ~ 0.7219 - 0.7321, ɛNd ~ -12 - -13.4) and MIS3,4(87Sr/86Sr ~ 0.7310 - 0.7354, ɛNd ~ -16 - -17.9) is suggested to be related with the provenance change of the detrital particles since LGM. The addition of detrital particle from Appalachians with less radiogenic 87Sr/86Sr and positive ɛNd altered the character of the sediment of the Mississippi River during the last glaciation and deglaciation. In the Brazos-Trinity Basin IV, the narrow range of 87Sr/86Sr and ɛNd indicate that the sediment source of Brazos-Trinity Basin IV had not changed obviously during MIS5e to MIS2, mostly from coastal rivers such as Brazos River, Trinity River and Sabine River. The pre-fan with 87Sr/86Sr ~0.735 and ɛNd ~ -14.5 to -16.9, which is very similar to the deep sediment in the Ursa Basin with 87Sr/86Sr ~0.733 to 0.735 and ɛNd ~ -16 to -18. It is suggested that sediments of the pre-fan of the Brazos-Trinity Basin IV were supplied from the ancestral Mississippi River Delta during the low sea level (MIS 6). During the MIS5, the discharge of Mississippi River is thought switched to its present course, ~300 km to the east.

  4. Ion microprobe analysis of Rb and Sr isotopes in K-rich minerals: an attempt of radiometric dating

    International Nuclear Information System (INIS)

    We report here in situ measurements of Rb and Sr isotopes in K-rich minerals (muscovite, phlogopite, and K-feldspar) using Sensitive High-Resolution Ion MicroProbe (SHRIMP). Several grains of the K-rich minerals were extracted from eight granitic rocks with various formation ages and mounted on epoxy-resin disks. Chemical compositions were measured by an electron probe microanalyzer (EPMA). Then they were set in the source chamber of SHRIMP. A 4-5 nA mass filtered O2- primary beam was used to sputter a 30-λm-diameter flat-bottomed crater and secondary positive ions were extracted by a 10 kV accelerating voltage for mass analysis. A mass resolution of 8900-9300 at 1% peak height was attained to reduce isobaric hydride interferences such as 87RbH+ on 88Sr+. The magnet was cyclically peak-stepped from mass 84 (84Sr and 28Si56Fe) to mass 88 (88Sr and 30Si58Fe), including the background, mass 85 for 85Rb ad 29Si56Fe, mass 86 for 86Sr and 30Si56Fe, and mass 87 for 87Rb, 87Sr, and 29Si58Fe, respectively. No SiFe compounds of any mass number contributed significantly for the samples analyzed. Observed 87A/85A ratios (where A is an arbitrary element) were plotted against 88A/85A ratios for each sample. A least-square fitting was made in the diagram. The gradient and Y-intercept correspond to initial 87Sr/88Sr and initial 87Rb/85Rb ratios or present (87Rb/85Rb) + (87Sr*/85Rb) ratios, respectively, where ''*'' denotes radiogenic. The initial 87Sr/88Sr ratios are mostly consistent with the upper mantle 87Sr/88Sr ratios of various ages within experimental error. There is a positive correlation between the initial 87Rb/85Rb ratios and formation ages of the granitic rock samples, as it is expected from 87Rb decay. Further evaluation of the instrumental isotopic mass fractionation and relative sensitivities for Rb and Sr are required before the in situ 87Rb-87Sr measurement is routinely applied as a dating method. (author)

  5. Geochemical research on C-O and Sr-Nd isotopes of mantle-derived rocks from Shandong Province, China

    Institute of Scientific and Technical Information of China (English)

    LIU; Jianming; ZHANG; Hongfu; SUN; Jinggui; YE; Jie

    2004-01-01

    This paper presents systematic studies on the C-O and Sr-Nd isotopic compositions for Cretaceous Badou carbonatites, Fangcheng basalts, and Jiaodong lamprophyres and Paleozoic Mengyin kimberlites in Shandong Province, China. Paleozoic kimberlites have normal and uniform C-O isotopic compositions with δ13C and δ18O in the range of -4.8‰--7.6‰ and +9.9‰-+13.2‰, respectively. However, Cretaceous three different types of mantle-derived rocks have quite different C-O isotopic compositions, indicating that the mantle sources are probably partially contaminated with organic carbon-bearing crustal materials. These Cretaceous rocks show uniform and EMII-like Sr-Nd isotopic compositions and also indicate that the mantle sources were affected by recycled crustal materials. Comparative studies of C-O and Sr-Nd isotopes reveal that the lithospheric mantle beneath the eastern North China Craton had different isotope characteristics in the Paleozoic, the early Cretaceous, and the Tertiary time. This demonstrates that the lithospheric mantle beneath the region underwent at least twice reconstructions since the Paleozoic. Available data imply that the first reconstruction mainly happened during the Triassic-Jurassic time with gradual changes and the second in the Cretaceous with abrupt changes. Results also show that the early Cretaceous (especially at 120-130 Ma) was perhaps the key period leading to the dramatic change of the Mesozoic geodynamics on the eastern North China Craton.

  6. Sr-Nd isotope geochemistry of eolian dust of the arid-semiarid areas in China: Implications for loess provenance and monsoon evolution

    Institute of Scientific and Technical Information of China (English)

    RAO Wenbo; YANG Jiedong; CHEN Jun; LI Gaojun

    2006-01-01

    Minerals and rocks have distinct 87Sr/86Sr and 143Nd/144Nd ratios, depending on their geological origin and ages, and these isotope ratios are less altered than elemental composition during transport in the atmosphere or after deposition as sediments, thus stable isotopes of Sr and Nd have great potential as tracers for provenance and transport of materials. During the hypergene process, Sr isotope ratios of sediments are controlled by their parent rocks, particle sizes and chemical weathering. In general, the higher the Sr isotope ratios of parent rocks, and/or the more the fine-grained fractions, and/or the stronger the chemical weathering, thus the higher the Sr isotope ratios of sediments. On the contrary, there are lower Sr isotope ratios of sediments. Nd isotope ratios of sediments, independent of their particle sizes and chemical weathering, are only associated with parent rocks. For the provenance of the Chinese Loess Plateau, different reseachers drew discordant and even contradictory conclusions by using the method of Sr-Nd isotopic tracing. From the previous Nd isotope data, it is considered that the Tarim Basin, deserts in the central and west parts of Inner Mongolia and the Tibetan Plateau are the main sources of the Chinese Loess Plateau, and are also manufacturers for eolian dust of the Far East regions, together with the Chinese Loess Plateau. Sr isotope ratios of eolian dust are solely affected by wind sorting and weathering-pedogenesis due to its homogeneous composition in the Chinese Loess Plateau. Wind sorting is related to the East Asian winter monsoon but weathering-pedogenesis is mainly associated with the East Asian summer monsoon. Studies on Sr isotopic compositions of the loess-paleosol sequence suggest that 87Sr/86Sr ratios in acid-soluble materials are an index for chemical weathering intensity of the Chinese Loess Plateau, indicating the East Asian summer monsoon variations, whereas 87Sr/86Sr ratios in acid-insoluble materials are

  7. Environmental isotopes (18O, 2H, and 87Sr/86Sr) as a tool in groundwater investigations in the Keta Basin, Ghana

    Science.gov (United States)

    Jørgensen, Niels; Banoeng-Yakubo, Bruce

    2001-03-01

    Analyses of environmental isotopes (18O, 2H, and 87Sr/86Sr) are applied to groundwater studies with emphasis on saline groundwater in aquifers in the Keta Basin, Ghana. The 87Sr/86Sr ratios of groundwater and surface water of the Keta Basin primarily reflect the geology and the mineralogical composition of the formations in the catchments and recharge areas. The isotopic compositions of 18O and 2H of deep groundwater have small variations and plot close to the global meteoric water line. Shallow groundwater and surface water have considerably larger variations in isotopic compositions, which reflect evaporation and preservation of seasonal fluctuations. A significant excess of chloride in shallow groundwater in comparison to the calculated evaporation loss is the result of a combination of evaporation and marine sources. Groundwaters from deep wells and dug wells in near-coastal aquifers are characterized by relatively high chloride contents, and the significance of marine influence is evidenced by well-defined mixing lines for strontium isotopes, and hydrogen and oxygen stable isotopes, with isotopic compositions of seawater as one end member. The results derived from environmental isotopes in this study demonstrate that a multi-isotope approach is a useful tool to identify the origin and sources of saline groundwater. Résumé. L'analyse des isotopes du milieu (18O, 2H, et 87Sr/86Sr) a été mise en œuvre pour des études hydrogéologiques portant sur des eaux souterraines salées des aquifères du bassin de Keta (Ghana). Les rapports isotopiques 87Sr/86Sr de l'eau souterraine et de l'eau de surface du bassin de Keta reflètent principalement la géologie et la composition minéralogique des formations des bassins d'alimentation et des zones de recharge. Les compositions isotopiques en 18O et en 2H des eaux souterraines profondes présentent de faibles variations et se placent près de la droite des eaux météoriques mondiales. Les eaux des nappes peu profondes

  8. Environmental isotopes (18O, 2H, and 87Sr/86Sr) as a tool in groundwater investigations in the Keta Basin, Ghana

    Science.gov (United States)

    Jørgensen, Niels; Banoeng-Yakubo, Bruce

    2001-03-01

    Analyses of environmental isotopes (18O, 2H, and 87Sr/86Sr) are applied to groundwater studies with emphasis on saline groundwater in aquifers in the Keta Basin, Ghana. The 87Sr/86Sr ratios of groundwater and surface water of the Keta Basin primarily reflect the geology and the mineralogical composition of the formations in the catchments and recharge areas. The isotopic compositions of 18O and 2H of deep groundwater have small variations and plot close to the global meteoric water line. Shallow groundwater and surface water have considerably larger variations in isotopic compositions, which reflect evaporation and preservation of seasonal fluctuations. A significant excess of chloride in shallow groundwater in comparison to the calculated evaporation loss is the result of a combination of evaporation and marine sources. Groundwaters from deep wells and dug wells in near-coastal aquifers are characterized by relatively high chloride contents, and the significance of marine influence is evidenced by well-defined mixing lines for strontium isotopes, and hydrogen and oxygen stable isotopes, with isotopic compositions of seawater as one end member. The results derived from environmental isotopes in this study demonstrate that a multi-isotope approach is a useful tool to identify the origin and sources of saline groundwater. Résumé. L'analyse des isotopes du milieu (18O, 2H, et 87Sr/86Sr) a été mise en œuvre pour des études hydrogéologiques portant sur des eaux souterraines salées des aquifères du bassin de Keta (Ghana). Les rapports isotopiques 87Sr/86Sr de l'eau souterraine et de l'eau de surface du bassin de Keta reflètent principalement la géologie et la composition minéralogique des formations des bassins d'alimentation et des zones de recharge. Les compositions isotopiques en 18O et en 2H des eaux souterraines profondes présentent de faibles variations et se placent près de la droite des eaux météoriques mondiales. Les eaux des nappes peu profondes

  9. Comprehensive Pb-Sr-Nd-Hf isotopic, trace element, and mineralogical characterization of mafic to ultramafic rock reference materials

    Science.gov (United States)

    Fourny, Anaïs.; Weis, Dominique; Scoates, James S.

    2016-03-01

    Controlling the accuracy and precision of geochemical analyses requires the use of characterized reference materials with matrices similar to those of the unknown samples being analyzed. We report a comprehensive Pb-Sr-Nd-Hf isotopic and trace element concentration data set, combined with quantitative phase analysis by XRD Rietveld refinement, for a wide range of mafic to ultramafic rock reference materials analyzed at the Pacific Centre for Isotopic and Geochemical Research, University of British Columbia. The samples include a pyroxenite (NIM-P), five basalts (BHVO-2, BIR-1a, JB-3, BE-N, GSR-3), a diabase (W-2), a dolerite (DNC-1), a norite (NIM-N), and an anorthosite (AN-G); results from a leucogabbro (Stillwater) are also reported. Individual isotopic ratios determined by MC-ICP-MS and TIMS, and multielement analyses by HR-ICP-MS are reported with 4-12 complete analytical duplicates for each sample. The basaltic reference materials have coherent Sr and Nd isotopic ratios with external precision below 50 ppm (2SD) and below 100 ppm for Hf isotopes (except BIR-1a). For Pb isotopic reproducibility, several of the basalts (JB-3, BHVO-2) require acid leaching prior to dissolution. The plutonic reference materials also have coherent Sr and Nd isotopic ratios (<50 ppm), however, obtaining good reproducibility for Pb and Hf isotopic ratios is more challenging for NIM-P, NIM-N, and AN-G due to a variety of factors, including postcrystallization Pb mobility and the presence of accessory zircon. Collectively, these results form a comprehensive new database that can be used by the geochemical community for evaluating the radiogenic isotope and trace element compositions of volcanic and plutonic mafic-ultramafic rocks.

  10. Nd and SR isotopic compositions of tektite material from Barbados and their relationship to North American tektites

    Science.gov (United States)

    Ngo, H. H.; Wasserburg, J.; Glass, B. P.

    1985-06-01

    The isotopic composition of microtektites from Barbados was determined to establish their possible source and their relationship to known tektite strewn fields. Analyzed samples included microtektites and tektite fragments from the Barbados oceanic beds, samples of deep sea ooze, in which they occur, and of underlying volcanic ash, as well as glass beads from Lake Wanapitei Crater. Isotope ratios (Sr-87/Sr-86, Nd-143/Nd-144, Rb-87/Sr-86, and Sm-147/Nd-144) were determined, and the epsilon values for Sr and Nd plotted on the diagram available for the fields of North America, Australia, Ivory Coast, and Moldavite tektites. The epsilon coordinates of all Barbados microtektite and bulk tektite samples plot precisely within the narrow field determined by North American tektites (epsilon Sr, 111; epsilon Nd, -6.2), yield an Nd model age of 0.6 AE, and are distinct from all other fields. The isotopic signatures of samples from sea ooze, ash layer, and of the Lake Wanapitei glass beads are clearly different from all known tektite classes. It is concluded that the Barbados tektites are of the same source and temporal event as the North American tektites.

  11. Sr, Nd, Pb and Hf isotopic constraints on mantle sources and crustal contaminants in the Payenia volcanic province, Argentina

    DEFF Research Database (Denmark)

    Søager, Nina; Holm, Paul Martin; Thirlwall, Matthew F.

    2015-01-01

    The presented Sr, Nd, Hf and double-spike Pb-isotopic analyses of Quaternary basalts from the Payenia volcanic province in southern Mendoza, Argentina, confirm the presence of two distinct mantle types feeding the Payenia volcanism. The southern Payenia mantle source feeding the intraplate-type Río...

  12. Sr-Nd isotope geology and tectonomagmatic setting of the Dehsalm intrusives (Lut Block, Eastern Iran)

    Science.gov (United States)

    Arjmandzadeh, Reza; Francisco Santos, Jose; Ribeiro, Sara

    2013-04-01

    The Dehsalm porphyritic shallow intrusives belong to the Lut Block volcanic-plutonic belt (central eastern Iran). Previous research on alteration, mineralization and hydrothermal fluids indicates that a Cu-Mo porphyry type mineralization system is related with these intrusives (Arjmandzadeh et al., 2012). The rocks studied in this work range in composition from gabbro-diorite to granite, with dominance of monzonites and quartz monzonites, and have geochemical features of high-K calc alkaline to shoshonitic volcanic arc suites. The trends of major element oxides on Harker diagrams, together with textural evidence, point to the crystal fractionation of clinopyroxene, Ca - plagioclase, hornblende, apatite and oxide minerals. Primitive mantle - normalized trace element spider diagrams display strong enrichment in LILE, such as Rb, Ba and Cs, and depletions in some high field strength elements (HFSE), such as Nb, Ti, Y and HREE. Chondrite-normalized plots show significant LREE enrichments, high LaN/YbN (21.5 to 31.0) and the lack of Eu anomaly. Sr/Y and La/Yb ratios of Dehsalm intrusives are respectively 31.6-72.2 and 21.5-33.5, which reveals that, despite their K-rich composition, these rocks also have some adakitic affinity. A Rb-Sr whole rock-feldspar-biotite age of 33.4±1 Ma was obtained in a quartz monzonite sample; this date may be interpreted as close to the intrusion age, considering that the chosen sample is almost unaltered and should have suffered fast cooling. The obtained age coincides, within error, with a previous geochronological result in a similar rock from the Chah-Shaljami area (Arjmandzadeh et al., 2011), further northwest along the eastern border of the Lut Block. 87Sr/86Sr(33Ma) and ɛNd(33Ma) values range from 0.70481 to 0.70508 and from +1.5 to +2.5, respectively, which fits into a supra-subduction mantle wedge source for the parental melts and indicates that crustal contribution for magma diversification was not relevant. Sr and Nd isotope

  13. High-Resolution Paleosalinity Reconstruction From Laguna de la Leche, North Coastal Cuba, Using Sr, O, and C Isotopes

    Science.gov (United States)

    Peros, M. C.; Reinhardt, E. G.; Schwarcz, H. P.; Davis, A. M.

    2008-12-01

    Isotopes of Sr, O, and C were studied from a 227-cm long sediment core to develop a high-resolution paleosalinity record to investigate the paleohydrology of Laguna de la Leche, north coastal Cuba, during the Middle to Late Holocene. Palynological, plant macrofossil, foraminiferal, ostracode, gastropod, and charophyte data from predominantly euryhaline taxa, coupled with a radiocarbon-based chronology, indicate that the wetland evolved through four phases: (1) an oligohaline lake existed from 6200 to 4800 cal yr B.P.; (2) water level in the lake increased and the system freshened from 4800 to 4200 cal yr B.P.; (3) a mesohaline lagoon replaced the lake 4200 cal yr B.P.; and (4) mangroves enclosed the lagoon beginning 1700 cal yr B.P., forming a mesohaline lake. Isotopic ratios were measured on specimens of the euryhaline foraminifer Ammonia beccarii, although several measurements were also made on other calcareous microfossils in order to identify potential taphonomic and/or vital effects. The 87Sr/86Sr results show that the average salinity of Laguna de la Leche was 1.7 ppt during the early lake phase and 8 ppt during the lagoon phase - a change driven by relative sea level rise. The delta18O results do not record the salinity increase seen in the 87Sr/86Sr data, but instead indicate high evaporation from the lake surface. Variability in delta13C was controlled by plant productivity, episodic marine incursions, and vegetation community change. There is some evidence for seasonal effect and the lateral transport of microfossils prior to burial. Our results show that Sr isotopes, while often cited as a powerful paleosalinity tool, should be used in conjunction with other indicators when investigating paleosalinity trends; relying solely on any single isotopic or ecological indicator can lead to inaccurate results, especially in semi-enclosed and closed hydrological systems.

  14. Late Cenozoic alkaline volcanism in the northwestern Caribbean - Tectonic setting and Sr isotopic characteristics

    Science.gov (United States)

    Wadge, G.; Wooden, J. L.

    1982-01-01

    The northwestern corner of the Caribbean plate has at least sixteen centers of alkalic volcanism, most of which is Quaternary in age. Sr-87/Sr-86 ratios of the rocks in these centers are used to distinguish three geographical groups: a low-ratio group (0.7026-0.7031) at the Nicaraguan Rise, an intermediate-ratio group (0.7036-0.7038) in northeastern Costa Rica, and a high-ratio group (0.7047-0.7063) in Hispaniola. It is suggested that the increased radiogenic strontium in both Costa Rica and Hispaniola may have come from volatile-rich fluids escaping from adjacent subducting slabs of oceanic crust. The isotopic differences between the two areas is explained by the relative longevity and high rate of subduction in Costa Rica compared to that in Hispaniola. The Costa Rican alkaline rocks cover a segment of the Cocos plate which is being subducted at a smaller angle (about 35 deg) than at the rest of the Central American arc.

  15. Microscopic study of low-lying yrast spectra and deformation systematics in neutron-rich 98−106Sr isotopes

    Indian Academy of Sciences (India)

    Anil Chandan; Suram Singh; Arun Bharti; S K Khosa

    2009-10-01

    Variation-after-projection (VAP) calculations in conjunction with Hartree–Bogoliubov (HB) ansatz have been carried out for = 98–106 strontium isotopes. In this framework, the yrast spectra with ≥ 10+, (2) transition probabilities, quadrupole deformation parameter and occupation numbers for various shell model orbits have been obtained. The results of the calculation for yrast spectra give an indication that it is important to include the hexadecapole–hexadecapole component of the two-body interaction for obtaining various nuclear structure quantities in Sr isotopes. Besides this, it is also found that the simultaneous polarization of 3/2 and 5/2 proton subshells is a significant factor in making a sizeable contribution to the deformation in neutron-rich Sr isotopes.

  16. Use of Sr and Pb isotopes in gneissic-migmatic rocks in Itacambira-Barrocao, MG, Brazil

    International Nuclear Information System (INIS)

    This work tries to show the potential of the Rb-Sr, Pb-Pb and K-Ar methods applied to basic geological mapping. The different interpretative values of these methodologies contribute to the understanding of the tectonic processes developed in the southeastern border of the Sao Francisco Craton. The Rb-Sr and Pb-Pb isotopic data for the gneissic-migmatitic unit of this sector indicates their generation during the Archean (-2.7 Ga) and Early Proterozoic (-2.1 Ga.). The high (Sr87 /Sr86) and μ1 values also suggest an origin through reworking of older crustal rocks. The K-Ar data (and one fission track age) allow the thermal history of this domain to be delineated and suggest a vertical tectonic in the Late Brazilian Cycle, putting side by side blocks formed in different depths. (M.V.M.)

  17. Hydrogeochemistry of the surface waters of the Ebro River Basin (Spain): a view through Li-B-Sr isotopes

    Science.gov (United States)

    Millot, R.; Guerrot, C.; Petelet-Giraud, E.; Brenot, A.; Negrel, P. J.

    2012-12-01

    In the present study, we report hydrogen, oxygen, lithium, boron and strontium isotope measurements (δ2H, δ18O, δ7Li, δ11B and 87Sr/86Sr) together with major and trace elements in the dissolved load of 25 river samples collected within the Ebro River Basin in Spain. The Ebro River Basin is mainly dominated by carbonates and evaporites from the Paleozoic and Mesozoic terrains. The Ebro river mainstream was sampled at Amposta one time per month between June 2005 and May 2006. And secondly, the Ebro river along its main course and its main tributaries were sampled during one field campaign in April 2006. The main objective of the present work is to characterize the hydrogeochemistry of the surface waters within the Ebro River Basin and to constrain the behavior of Li and B and their isotopes during water/rock interactions at the scale of a large river basin having various lithologies with a specific aim to investigate spatio-temporal variations for both Li and B isotopes signatures within the Ebro River Basin. The main goal of this study is thus to determine the sources contributing to Li and B in the river waters of the Ebro Basin, as well as to characterize the controlling factors that can determine the distribution of Li and B and their isotopes in the river waters of the Ebro Basin. Stable water isotopes (δ2H, δ18O) show that all the river waters have a purely local origin from precipitation, without significant evaporation or water/rock interaction, as all points plot close to the general meteoric-water line. In the river waters, Li isotopic signatures (δ7Li) are comprised between +12.9 and +20.9‰, δ11B values are ranging from +9.9 to +25.0‰ and 87Sr/86Sr are between 0.70786 and 0.70897.

  18. The crust role at Paramillos Altos intrusive belt: Sr and Pb isotope evidence

    International Nuclear Information System (INIS)

    Paramillos Altos Intrusive Belt (PAIB) (Ostera, 1996) is located in the thick skinned folded-thrust belt of Malargue, southwestern Mendoza, Argentina. Geochemical, geochronologic and isotopic studies were carried out in it (Ostera 1996, 1997, Ostera et al. 1999; Ostera et al. 2000) and these previous papers suggested a minor involvement of the crust in the genesis of the PAIB. According with Ostera et al. (2000) it is composed by stocks, laccoliths, dykes and sills which range in composition from diorites to granodiorites, and from andesites to rhyolites, and divided in five Members, which range in age from Middle Miocene to Early Miocene: a- Calle del Yeso Dyke Complex (CYDC), with sills and dykes of andesitic composition (age: 20±2 Ma). b- Puchenque-Atravesadas Intrusive Complex (PAIC), composed by dykes and stocks ranging from diorites to granodiorites (age: 12.5±1 Ma). c- Arroyo Serrucho Stock (SAS), an epizonal and zoned stock, with four facies, with K/Ar and Ar/Ar dates of 10±1 and 9.5±0.5 Ma. d- Portezuelo de los Cerros Bayos (PCB), that includes porphyritic rocks of rhyolitic composition, of 7.5±0.5 Ma. e- Cerro Bayo Vitrophyres (CBV), with andesitic sills and dykes (age: 4.8±0.2 Ma). We present in this paper new Sr and Pb isotopes data that constrain the evolution of the PAIB (au)

  19. Combination of the (87)Sr/(86)Sr ratio and light stable isotopic values (δ(13)C, δ(15)N and δD) for identifying the geographical origin of winter wheat in China.

    Science.gov (United States)

    Liu, Hongyan; Wei, Yimin; Lu, Hai; Wei, Shuai; Jiang, Tao; Zhang, Yingquan; Guo, Boli

    2016-12-01

    This study aims to investigate whether isotopic signatures can be used to develop reliable fingerprints for discriminating the geographical origin of Chinese winter wheat, and to evaluate the discrimination effects of δ(13)C, δ(15)N and δD, alone or with (87)Sr/(86)Sr. In this study, the values of δ(13)C, δ(15)N and δD, and the (87)Sr/(86)Sr ratios of wheat and provenance soils from three regions were determined. Significant differences were found in all parameters of wheat and (87)Sr/(86)Sr in soil extract (reflecting the bioavailable fraction of soil) among different regions. A significantly positive correlation was observed between the (87)Sr/(86)Sr ratios of wheat and soil extracts. An overall correct classification rate of 77.8% was obtained for discriminating wheat from three regions based on light stable isotopes (δ(13)C, δ(15)N, and δD). The correct classification rate of 98.1% could be obtained with the combination of the (87)Sr/(86)Sr ratio and the light stable isotopic values. PMID:27374544

  20. Using Monte Carlo transport to accurately predict isotope production and activation analysis rates at the University of Missouri research reactor

    International Nuclear Information System (INIS)

    A detailed Monte Carlo N-Particle Transport Code (MCNP5) model of the University of Missouri research reactor (MURR) has been developed. The ability of the model to accurately predict isotope production rates was verified by comparing measured and calculated neutron- capture reaction rates for numerous isotopes. In addition to thermal (1/v) monitors, the benchmarking included a number of isotopes whose (n, γ) reaction rates are very sensitive to the epithermal portion of the neutron spectrum. Using the most recent neutron libraries (ENDF/ B-VII.0), the model was able to accurately predict the measured reaction rates in all cases. The model was then combined with ORIGEN 2.2, via MONTEBURNS 2.0, to calculate production of 99Mo from fission of low-enriched uranium foils. The model was used to investigate both annular and plate LEU foil targets in a variety of arrangements in a graphite irradiation wedge to optimize the production of 99Mo. (author)

  1. Stable (Cu, Mg) and radiogenic (Sr, Nd) isotope fractionation in colloids of boreal organic-rich waters

    International Nuclear Information System (INIS)

    Stable (Cu and Mg) and radiogenic (Sr and Nd) isotopic compositions in filtrates and ultra filtrates of various size fractions have been measured in waters of subarctic watersheds (NW Russia) and in temperate rivers and lakes of the south boreal zone. A large volume of samples were filtered in the field using cascade filtration and ultrafiltration employing progressively decreasing pore sizes (100, 20, 10, 5, 0.8, 0.4, 0.22, and 0.1 μm; 100, 10 and 1 kDa) followed by element isotopic analysis using thermal ionization mass spectrometers and a Neptune multi collector ICP-MS. In the boreal watershed underlain by Archean and Proterozoic rocks, the 87Sr/86Sr ratio decreased in the 1-100 kDa ultra filtrates and dialysates by 0.0001-0.0004 units compared to the 0.45 μm filtrates. Despite the dominance of colloids in the Nd speciation in surface waters, the isotopic value of Nd in the filtrates and ultra filtrates remained constant within the uncertainty of the measurements. We hypothesize the absence of an atmospheric input of silicate dust for Nd but the presence of marine aerosols for Sr. It follows that the Sr in the investigated surface waters has a short residence time compared to the time required for achieving isotopic equilibrium between the colloidal (1 kDa-0.22 μm) and truly dissolved (≤1 kDa) pools. For Nd, the residence time is long enough to achieve this equilibrium. The stable isotope composition of Cu in the streams remained constant within ±0.1 per thousand during filtration through 100 μm to 1 kDa membranes, despite the fact that 40-60% of Cu was colloidal. This result suggests that the homogeneity of the Cu isotopic composition within the colloidal and truly dissolved pools is likely associated with the similarity of the structure and stability of Cu(II) complexes with fulvic acids of different molecular weights. The stable isotope composition of dissolved Mg in soil solution and bog surface water demonstrates similar,within the analytical

  2. A study of REE and Pb, Sr and Nd isotopes in garnet-lherzolite xenoliths from Mingxi, Fujian Province

    Science.gov (United States)

    Wankang, H.; Junwen, W.; Basu, A.R.; Tatsumoto, M.

    1993-01-01

    The REE and Pb, Sr, Nd isotopes in three xenoliths from limburgite and scoria-breccias, including spinel-lherzolite, spinel-garnet-lherzolite and phlogopite-gamet-lherzolite, were analysed. The REE contents of the xenoliths are 1.3 to 3.3 times those of the chondrites with their REE patterns characterized by weak LREE depletion. The143Nd/144Nd values of whole rocks and minerals range from 0.51306 to 0.51345 with ??Nd=+ 8.2- +15.8,206Pb/204 Pb < 18.673, and207Pb/204Pb < 15.574. All this goes to show that the upper mantle in Mingxi at the depth of 67-82 km is a depleted mantle of MORB type, with87Sr/86 Sr ratios 0.70237-0.70390. In Nd-Sr diagram the data points of whole rocks are all out of the mantle array, implying that the xenoliths from Mingxi have more radiogenic Sr isotopes than those of the mantle array. ?? 1993 Institute of Geochemistry, Chinese Academy of Sciences.

  3. Origin and Dynamics of Rare Earth Elements during Flood Events in Contaminated River Basins: Sr-Nd-Pb Isotopic Evidence.

    Science.gov (United States)

    Hissler, Christophe; Stille, Peter; Iffly, Jean François; Guignard, Cédric; Chabaux, François; Pfister, Laurent

    2016-05-01

    In order to precisely quantify the contribution of anthropogenic activities and geogenic sources to the dissolved and suspended loads of rivers we have combined for the first time Rare Earth Element (REE) concentrations with Sr-Nd-Pb isotope ratios. We observed enrichments in Anthropogenic Rare Earth Elements (AREE) for dissolved (Gd) and suspended (Ce and Nd) loads of river water. During flood events, AREE anomalies progressively disappeared and gave way to the geogenic chemical signature of the basin in both dissolved and suspended loads. The isotopic data confirm these observations and shed new light on the trace elements sources. On the one hand, dissolved loads have peculiar isotopic characteristics and carry mainly limestone-derived and anthropogenic Sr and Nd as well as significant amounts of anthropogenic Pb. On the other hand, the results clearly indicate that anthropogenic contributions impact the suspended loads in all hydrological conditions. This study demonstrates that anthropogenic contributions to the river may change not only Pb but also Sr and Nd isotopic compositions in both dissolved and suspended loads. This is of importance for future provenance studies. PMID:27045616

  4. Sr-Nd isotope geochemistry and petrogenesis of the Chah-Shaljami granitoids (Lut Block, Eastern Iran)

    Science.gov (United States)

    Arjmandzadeh, R.; Karimpour, M. H.; Mazaheri, S. A.; Santos, J. F.; Medina, J. M.; Homam, S. M.

    2011-05-01

    Chah-Shaljami porphyritic granitoids belong to the Lut Block volcanic-plutonic belt of central eastern Iran. These intrusive rocks are mostly quartz monzonites, granodiorites and diorites. Geochemical evidence reveals that they are co-genetic and that they have features typical of high-K calc-alkaline to shoshonitic rocks from volcanic arc setting. Primitive mantle-normalized trace element spider diagrams display strong enrichment in LILE, such as Rb, Ba, and Cs, and depletion in some HFSE, e.g. Nb, Ti, Y and HREE. Chondrite-normalized plots show a very marked REE fractionation, with significant LREE enrichment (23 ⩾ La N/Yb N ⩾ 14) and the lack of Eu anomaly. Sr/Y and La/Yb ratios of Chah-shaljami intrusives are respectively 20-67 and 21-34, which reveals that, despite their K-rich composition, these rocks also, have some adakitic affinity. Plots on the Sr/Y-Y and La/Yb-Yb diagrams show that the Chah-Shaljami intrusives may be subdivided into two distinct classes. A Rb-Sr age of 33.5 ± 1 Ma, mainly dependent on the Sr isotopic composition of biotite, was obtained in a quartz monzonite sample. Taking into account that this sample was almost unaffected by hydrothermal and meteoric alteration and that cooling was probably fast, the 33-34 Ma date is interpreted as the intrusion age. With the exception of two samples, initial 87Sr/ 86Sr ratios and C̵Nd values are clustered in the restricted ranges of 0.70470-0.70506 and +1.9-+2.7, which fits into a supra-subduction mantle wedge source for the parental melts and indicates that, in general, crustal contribution for magma diversification was not relevant; however, one sample shows higher 87Sr/ 86Sr and lower C̵Nd, revealing that, occasionally, crustal rock assimilation also contributed to geochemical variation; one other sample, strongly affected by hydrothermal alteration, departs from the main group only by higher 87Sr/ 86Sr, suggesting that its alteration involved crustal fluids. Sr and Nd isotope compositions

  5. Contrasting Sr isotope ratios in plagioclase from different formations of the mid-Miocene Columbia River Basalt Group

    Science.gov (United States)

    Starkel, W. A.; Wolff, J.; Eckberg, A.; Ramos, F.

    2008-12-01

    Many early Columbia River Basalt flows of the Steens and Imnaha Formations are characterized by abundant, texturally complex, coarse plagioclase phenocrysts. In Imnaha lavas, the feldspars typically have more radiogenic 87Sr/86Sr than whole rock and matrix, and may exhibit complex isotopic zoning that is not correlated with An content. Imnaha plagioclase grains are interpreted as variably-contaminated crystals produced when high-crystallinity mid-crustal basaltic intrusions exchanged interstitial melt with adjacent partly-melted crustal rock; this isotopically variable debris was then remobilized by subsequent intrusion of mantle-derived basalt and brought to the surface as an isotopically heterogeneous mixture. In contrast, plagioclase grains in the texturally very similar Steens lavas are isotopically near-homogeneous and 87Sr/86Sr is not significantly displaced from that of the bulk rock. This is consistent with magma- crust interaction at low degrees of crustal melting during the early stages of the Columbia River flood basalt episode, where Steens and Imnaha lavas were erupted from distinct magma systems hosted by different types of crust that exerted different degrees of isotopic leverage on the mantle-derived magmas [1]. Thermal input to the Steens system declined at the same time as the Imnaha magmatic flux increased to ultimately produce the huge outpouring of Grande Ronde lavas, which are mixtures of mantle- and crust-derived liquids, the latter produced during high degrees of crustal melting during the time of peak magmatic flux. [1] Wolff et al. (2008) Nature Geoscience 1, 177-180.

  6. Hydrogeochemistry of the surface waters of the Ebro River Basin (Spain): a view through Li-B-Sr isotopes

    OpenAIRE

    Millot, Romain; Guerrot, Catherine; Petelet Giraud, Emmanuelle; Brenot, Agnès; Négrel, Philippe

    2012-01-01

    In the present study, we report hydrogen, oxygen, lithium, boron and strontium isotope measurements (d2H, d18O, d7Li, d11B and 87Sr/86Sr) together with major and trace elements in the dissolved load of 25 river samples collected within the Ebro River Basin in Spain. The Ebro River Basin is mainly dominated by carbonates and evaporites from the Paleozoic and Mesozoic terrains. The Ebro river mainstream was sampled at Amposta one time per month between June 2005 and May 2006. And secondly, the ...

  7. Nd and Sr isotope compositions in modern and fossil bones - Proxies for vertebrate provenance and taphonomy

    Science.gov (United States)

    Tütken, Thomas; Vennemann, Torsten W.; Pfretzschner, Hans-U.

    2011-10-01

    Rare earth elements (REE), while not essential for the physiologic functions of animals, are ingested and incorporated in ppb concentrations in bones and teeth. Nd isotope compositions of modern bones of animals from isotopically distinct habitats demonstrate that the 143Nd/ 144Nd of the apatite can be used as a fingerprint for bedrock geology or ambient water mass. This potentially allows the provenance and migration of extant vertebrates to be traced, similar to the use of Sr isotopes. Although REE may be enriched by up to 5 orders of magnitude during diagenesis and recrystallization of bone apatite, in vivo143Nd/ 144Nd may be preserved in the inner cortex of fossil bones or enamel. However, tracking the provenance of ancient or extinct vertebrates is possible only for well-preserved archeological and paleontological skeletal remains with in vivo-like Nd contents at the ppb-level. Intra-bone and -tooth REE analysis can be used to screen for appropriate areas. Large intra-bone Nd concentration gradients of 10 1-10 3 are often measured. Nd concentrations in the inner bone cortex increase over timescales of millions of years, while bone rims may be enriched over millenial timescales. Nevertheless, ɛ Nd values are often similar within one ɛ Nd unit within a single bone. Larger intra-bone differences in specimens may either reflect a partial preservation of in vivo values or changing ɛ Nd values of the diagenetic fluid during fossilization. However, most fossil specimens and the outer rims of bones will record taphonomic 143Nd/ 144Nd incorporated post mortem during diagenesis. Unlike REE patterns, 143Nd/ 144Nd are not biased by fractionation processes during REE-uptake into the apatite crystal lattice, hence the ɛ Nd value is an important tracer for taphonomy and reworking. Bones and teeth from autochthonous fossil assemblages have small variations of ±1 ɛ Nd unit only. In contrast, fossil bones and teeth from over 20 different marine and terrestrial fossil

  8. A Robust and Fully-Automated Chromatographic Method for the Quantitative Purification of Ca and Sr for Isotopic Analysis

    Science.gov (United States)

    Smith, H. B.; Kim, H.; Romaniello, S. J.; Field, P.; Anbar, A. D.

    2014-12-01

    High throughput methods for sample purification are required to effectively exploit new opportunities in the study of non-traditional stable isotopes. Many geochemical isotopic studies would benefit from larger data sets, but these are often impractical with manual drip chromatography techniques, which can be time-consuming and demand the attention of skilled laboratory staff. Here we present a new, fully-automated single-column method suitable for the purification of both Ca and Sr for stable and radiogenic isotopic analysis. The method can accommodate a wide variety of sample types, including carbonates, bones, and teeth; silicate rocks and sediments; fresh and marine waters; and biological samples such as blood and urine. Protocols for these isotopic analyses are being developed for use on the new prepFAST-MCTM system from Elemental Scientific (ESI). The system is highly adaptable and processes up to 24-60 samples per day by reusing a single chromatographic column. Efficient column cleaning between samples and an all Teflon flow path ensures that sample carryover is maintained at the level of background laboratory blanks typical for manual drip chromatography. This method is part of a family of new fully-automated chromatographic methods being developed to address many different isotopic systems including B, Ca, Fe, Cu, Zn, Sr, Cd, Pb, and U. These methods are designed to be rugged and transferrable, and to allow the preparation of large, diverse sample sets via a highly repeatable process with minimal effort.

  9. Nd isotopic composition of Jurassic Tethys seawater and the genesis of Alpine Mn-deposits: Evidence from Sr-Nd isotope data

    Science.gov (United States)

    Stille, P.; Clauer, N.; Abrecht, J.

    1989-05-01

    Jurassic metabasalts, metasediments and Mn ores from the Pennine realm of the Alps were examined in order to establish the Nd isotopic composition of the Jurassic Tethys seawater and to elucidate the genesis of the Mn deposits. The highly positive initial ɛNd values (+7 to +9.8) of the metabasalts and their low 87Sr /86Sr ratios (0.7028 to 0.7049) indicate that they originated from a depleted mantle. The initial ɛNd values of the cherts range between -5 and -9. The Sm-Nd isotope data indicate that they are primary mixtures of basalt and continental detritus. The smaller than 2 μm fractions of the cherts and of a marble, which probably represent the formerly authigenic material, show initial ɛnd values ranging between -5.9 and -6.6. The average initial Sr isotopic composition of five Mn ores is 0.70730 ± 22, identical to that of contemporaneous Jurassic seawater. The initial Nd isotopic composition values of the Mn ores are very homogeneous. The average value of five ores, a leachate and residue of one of them, calculated for an age of 170 Ma, is 0.512082± 19. It is suggested that the ores, together with the smaller than 2μm fractions of the sediments, define the Jurassic Tethys seawater isotopic composition. The resulting average 143Nd /144Nd initial value is 0.512089 ± 17 ( ɛNd -6.5 ± 0.6).

  10. Nd isotopic composition of Jurassic Tethys seawater and the genesis of Alpine Mn-deposits: Evidence from Sr-Nd isotope data

    Energy Technology Data Exchange (ETDEWEB)

    Stille, P.; Clauer, N. (Universite Louis Pasteur, Strasbourg (France)); Abrecht, J. (Univ. of Basel (Switzerland))

    1989-05-01

    Jurassic metabasalts, metasediments and Mn ores from the Pennine realm of the Alps were examined in order to establish the Nd isotopic composition of the Jurassic Tethys seawater and to elucidate the genesis of the Mn deposits. The highly positive initial {epsilon}{sub Nd} values (+7 to +9.8) of the metabasalts and their low {sup 87}Sr/{sup 86}Sr ratios (0.7028 to 0.7049) indicate that they originated from a depleted mantle. The initial {epsilon}{sub Nd} values of the cherts range between {minus}5 and {minus}9. The Sm-Nd isotope data indicate that they are primary mixtures of basalt and continental detritus. The smaller than 2 {mu}m fractions of the cherts and of a marble, which probably represent the formerly authigenic material, show initial {epsilon}{sub Nd} values ranging between {minus}5.9 and {minus}6.6. The average initial Sr isotopic composition of five Mn ores is 0.70730 {plus minus} 22, identical to that of contemporaneous Jurassic seawater. The initial Nd isotopic composition values of the Mn ores are very homogeneous. The average value of five ores, a leachate and residue of one of them, calculated for an age of 170 Ma, is 0.512082 {plus minus} 19. It is suggested that the ores, together with the smaller than 2 {mu}m fractions of the sediments, define the Jurassic Tethys seawater isotopic composition. The resulting average {sup 143}Nd/{sup 144}Nd initial value is 0.512089 {plus minus} 17 ({epsilon}{sub Nd} {minus}6.5 {plus minus} 0.6).

  11. Rb-Sr Isotopic Systematics of Alkali-Rich Fragments in the Yamato-74442 LL-Chondritic Breccia

    Science.gov (United States)

    Yokoyama, T.; Misawa, K.; Okano, O.; Shih, C.-Y.; Nyquist, L. E.; Simo, J. I.; Tappa, M. J.; Yoneda, S.

    2012-01-01

    Alkali-rich igneous fragments were identified in the brecciated LL-chondrites, Kr henberg (LL5)], Bhola (LL3-6) and Yamato (Y)-74442 (LL4), and show characteristic fractionation patterns of alkaline elements. The K-Rb-Cs-rich fragments in Kr henberg, Bhola, and Y-74442 are very similar in mineralogy and petrography (olivine + pyroxene + glass), suggesting that they could have come from related precursor materials. We have undertaken Rb-Sr isotopic studies on alkali-rich fragments in Y-74442 to precisely determine their crystallization ages and the isotopic signatures of their precursor material(s).

  12. Archean and proterozoic in the West-European Hercynian chain: isotopic geochemistry (Sr-Nd-Pb) and U-Pb geochronology on zircons

    International Nuclear Information System (INIS)

    The first part of this research thesis reports the study of isotopic (Sr-Nd-Pb) geochemistry and U-Pb geochronology on zircons in the immersed granulites of the Bay of Biscay: U-Pb geochronology on zircons, Nd isotopic geochemistry, Sr isotopic geochemistry, common Pb, Rb-Sr, Sm-Nd and rare earth data on minerals, comparison with other European granulites, comparison with West-Africa, study of Archean and proterozoic in the Hercynian chain. The second part reports the study of the U-Pb geochronology on zircon in the Cadomian, and the third part addresses the Sr-Nd isotopic geochemistry of some Cadomian granitoid, and the crust contamination in different regions

  13. Cooling of Sr to high phase-space density by laser and sympathetic cooling in isotopic mixtures

    OpenAIRE

    Ferrari, G; Drullinger, R. E.; Poli, N.; Sorrentino, F.; Tino, G. M.

    2006-01-01

    Based on an experimental study of two-body and three-body collisions in ultracold strontium samples, a novel optical-sympathetic cooling method in isotopic mixtures is demonstrated. Without evaporative cooling, a phase-space density of $6\\times10^{-2}$ is obtained with a high spatial density that should allow to overcome the difficulties encountered so far to reach quantum degeneracy for Sr atoms.

  14. Pervasive Crustal Melting on a Regional Scale: Sr-Nd Isotopic Evidence from Eocene Intrusions in NE Washington

    Science.gov (United States)

    Loewen, M. W.; Tepper, J. H.; Asmerom, Y.

    2007-12-01

    During the Eocene the Pacific Northwest was the site of a short-lived but voluminous and geochemically diverse magmatic episode, commonly termed the Challis event. To investigate the origins of this event we have measured whole rock Sr and Nd isotopic compositions of 12 plutonic and hypabyssal samples, ranging from basalt to two-mica granite, collected along a 250 km transect across NE Washington. This transect crosses the 0.706 line (Armstrong 1977), the boundary between dominantly Mesozoic crust to the west and older crust to the east. The results reveal a wide spread in isotopic compositions (87Sr/86Srm = 0.7041 - 0.7262; ɛNdm = +3.8 to -18.5) with no systematic relationship between isotopic composition and bulk composition (e.g., MgO). This decoupling of isotopic composition and bulk chemistry suggests mixing between mantle and crustal melts was of minimal importance, and that these rocks are dominantly of crustal origin. The range in ɛNdm also indicates melting of crustal sources that varied considerably in age. Samples with ɛNdm > +2 range from basalt (13 wt.% MgO) to two-mica granite (0.3 wt.% MgO). Such juvenile ɛNdm in a two-mica granite precludes significant involvement of ancient metasedimentary material and implies rapid intracrustal differentiation of a mantle-derived source, which may have been deep arc crust of Mesozoic age. At the other end of the spectrum, samples with ɛNdm Monzonite and attributed to melting of late Archean to Early Proterozoic crust (Whitehouse et al. 1992). Other samples analyzed in this study are broadly similar in isotopic composition (ɛNdm = +1 to -8; 87Sr/86Srm = 0.706-0.709) to rocks of the Colville Igneous Province and probably formed by melting of Proterozoic arc crust (Morris 2000). Geographic variability in Sr-Nd data indicates that isotopically distinct crustal domains are juxtaposed laterally and/or vertically, in some cases on a small scale. The sample with the highest 87Sr/86Srm (0.7262; ɛNdm = -13.3) is a

  15. Isotopic evidence for the retention of Sr-90 inferred from excess Zr-90 in the Oklo natural fission reactors: Implication for geochemical behaviour of fissiogenic Rb, Sr, Cs and Ba

    Science.gov (United States)

    Hidaka, Hiroshi; Sugiyama, Takeshi; Ebihara, Mitsuru; Holliger, Philippe

    1994-03-01

    In order to investigate the mobility of fissiogenic Sr-90 in the geological environment, the Zr isotopic compositions of seven samples from one of the newly formed Oklo natural reactor zones (i.e., reactor core and adjacent rocks (10, SF84)) in the Republic of Gabon were determined with an inductively coupled plasma mass spectrometer (ICP-MS). Zr isotopes in uraninite grains from different reactor zones were also measured by secondary ion mass spectrometry (SIMS). Fissiogenic Zr isotopic abundances of three samples from the reactor core have excess Zr-90, which has never before been formed in previous Oklo samples. In this paper, the geochemical behaviour of Zr-90 is discussed by making use of the relative retentivity inferred from the isotopic abundance of Sr. The excess in Zr-90 suggests dependence on the degree of retention/migration of Sr-90, the precursor of Zr-90 in the fission chain. In the aqueous phase, chemical fractionation between Sr and Zr could have occurred before radioactive Sr-90 decayed. Considering the halflife of Sr-90 (t(sub 1/2) = 29.1 y), considerable amounts of the latter have been produced during criticality. Sr and Zr (including Zr-90) could have been redistributed between the reactor core and its vicinity. The retentivity of fissiogenic Zr-90 in reactor core 10 is not homogeneous. In addition, the distributions of Rb, Cs and Ba is also heterogeneous.

  16. The geographic distribution of Sr isotopes from surface waters and soil extracts over the island of Bornholm (Denmark) – A base for provenance studies in archaeology and agriculture

    International Nuclear Information System (INIS)

    Highlights: • Establishment of distribution map of bioavailable strontium signatures on Bornholm. • Surface water and soil extract signatures incompletely reflect basement geology. • Baselines allow distinction between a northern and southern provenance on Bornholm. • Marine salts have a strong influence on bioavailable strontium signatures. • Successful application of baselines to the Grødbygård archaelogical site on Bornholm. - Abstract: In this paper we report the Sr isotope signatures, and Sr, Al and Na concentrations of 30 surface waters (lakes/ponds and rivers/creeks) and 19 soil sample extracts from the island of Bornholm (Denmark) and present a categorized 87Sr/86Sr value distribution map that may serve as a base for provenance studies, including archaeological migration and authenticity proof for particular food products. The Sr isotopic compositions of surface waters range from 87Sr/86Sr = 0.7097–0.7281 (average 0.7175 ± 0.0049; 1σ), whereas 0.1 M HNO3, 0.05 M HNO3, and 0.01 M CaCl2 soil extracts range from 87Sr/86Sr = 0.7095–0.7197 and define somewhat lower but statistically indistinguishable averages of 0.7125 ± 0.003 (1s). These compositions are lower than the values expected from the Precambrian granitoid basement (87Sr/86Sr = 0.758–0.944), and from the overlying, mainly clastic Paleozoic sediments. Combined Sr isotope composition vs. Sr, Na and Al concentration relationships of soil extracts imply that lowering of the isotopic composition of leachable Sr on Bornholm results as a consequence of significant admixture to this fraction of Sr deposited as marine salts (aerosols), and that rainwater only has a minor influence on the Sr budget of the surface waters. Positively correlated Al/Na and [1/Sr] vs. 87Sr/86Sr relationships in soil extracts and surface waters indicate that the surface run-off on Bornholm is characterized by two predominant sources, namely marine aerosols (sea salts) with high Sr and low 87Sr/86Sr values, and a

  17. Geochemical proxies of ocean circulation and weathering inputs: Radiogenic isotopes of Nd, Pb, Sr, Hf, and Os

    Energy Technology Data Exchange (ETDEWEB)

    Frank, Martin, E-mail: mfrank@ifm-geomar.de [IFM-GEOMAR, Leibniz Institute of Marine Sciences at the University of Kiel, Wischhofstrasse 1-3, 24148 Kiel (Germany)

    2011-05-15

    Marine records of the radiogenic isotope composition of the elements neodymium (Nd), lead (Pb), hafnium (Hf), strontium (Sr), and osmium (Os) allow the reconstruction of past continental weathering inputs on different time scales as a function of their respective oceanic residence times. Sr and Os have oceanic residence times significantly longer than the global mixing time of the ocean and are efficiently mixed on a global scale. Their isotope composition changes on long time scales as a function of plate tectonics and major orogenies, which allows their use as precise stratigraphic tools for the entire Phanerozoic. In contrast, Hf, Pb, and in particular Nd, have residence times on the order of or shorter than the global mixing time of the ocean, which results in distinct isotopic signatures of water masses and allows the reconstruction of past water mass mixing and weathering inputs on both long and short time scales. Here applications of these isotopes systems with a focus on the shorter residence time tracers are reviewed (without claiming to be comprehensive) and problems and potential solutions are discussed.

  18. Pb-Sr-O-C isotope compositions of metacarbonate rocks of the Derbina Formation (East Sayan): Chemostratigraphic and geochronological significance

    Science.gov (United States)

    Gorokhov, I. M.; Kuznetsov, A. B.; Ovchinnikova, G. V.; Nozhkin, A. D.; Azimov, P. Ya.; Kaurova, O. K.

    2016-01-01

    The Pb-Sr-O-C isotope compositions of calcite marbles of the Derbina Formation, exposed in the northwestern part of the Derbina block of the East Sayan, were studied. Rocks of the Derbina Formation were metamorphosed under high-temperature amphibolite facies conditions. The carbonate constituent of marbles contains (ppm) 15-130 Mn, 130-160 Fe, 0.008-0.039 Rb, 645-2190 Sr, 0.565-0.894 U, and 0.288-1.42 Pb. These concentrations are similar to those in modern carbonate sediments. The values of δ13C in marbles of the Derbina Formation range from-0.6 to +1.4‰ PDB; the values of δ18O range from 21.5 to 28.6‰ SMOW. The 87Sr/86Sr ratio values in the two least altered rocks, which meet geochemical criteria of the Rb-Sr system preservation in high-grade carbonate rocks, are 0.70804 and 0.70829. The protolith ages of marbles determined using Sr and C chemostratigraphy lie within the interval of 560-530 Ma, which is regarded as the period of carbonate sedimentation. The slope of the straight line on the 206Pb/204Pb-207Pb/204Pb diagram ( n = 9, MSWD = 19) constructed on the basis of the data points of bulk carbonate constituents of all samples studied and those representing leachate steps of one of them in 0.5N HBr yields Late Vendian age (556 ± 31 (2σ) Ma. Taking into account the data on Sr and C isotope systematics of Derbina marbles, this age is regarded as the age of early diagenesis of carbonate sediments close to the age of sedimentation. Thus, metacarbonate rocks of the Derbina Formation preserved the pre-metamorphic chemostratigraphic and isotope-geochronological information. The age obtained testifies that formation of the carbonate cover of the Derbina block occurred in the Late Vendian. At the end of the Cambrian, carbonate deposits were metamorphosed during the Early Caledonian tectonic event in the southeastern part of the Central Asian Fold Belt.

  19. Rb-Sr and Sm-Nd isotope geochemistry and chronology of cherts from the Onverwacht Group (3.5 AE), South Africa

    Science.gov (United States)

    Weis, D.; Wasserburg, G. J.

    1987-01-01

    An Rb-Sr and Sm-Nd isotopic analysis of Archean chert samples from the Onverwacht Group, South Africa is presented, showing the same characteristic Rb and Sr concentrations as Phanerozoic cherts, with a very large range of Rb-87/Sr-86 ratios. A good correlation line in the Rb-87 to Sr-87 evolution diagram, corresponding to an age of about 2119 My and an initial Sr-87/Sr-86 ratio of about 0.72246, is derived which may be interpreted as reflecting the age of rehomogenization of the Sr in the protolith and the recrystallization of these cherts due to circulating hydrothermal fluids during regional metamorphism about 1.4 AE after deposition of the Onverwacht Group. The Sm-Nd systematics reflect an ancient source age of about 3.5 AE.

  20. Comparative behavior of Sr, Nd and Hf isotopic systems during fluid-related deformation at middle crust levels

    Science.gov (United States)

    Luais, Béatrice; Le Carlier de Veslud, Christian; Géraud, Yves; Gauthier-Lafaye, François

    2009-05-01

    We have carried out a comparative Rb-Sr, Sm-Nd and Lu-Hf isotopic study of a progressively deformed hercynian leucogranite from the French Massif Central, belonging to the La Marche ductile shear zone, in order to investigate the respective perturbation of these geochronometers with fluid induced deformation. The one-meter wide outcrop presents a strongly deformed and mylonitized zone at the center, and an asymmetric deformation pattern with a higher deformation gradient on the northern side of the zone. Ten samples have been carefully collected every 10 cm North and South away from the strongest deformed mylonitic zone. They have been analyzed for a complete major, trace element data set, oxygen isotopes, Rb-Sr, Sm-Nd and Lu-Hf isotopic systematics. We show that most of major and trace elements except SiO 2, alkaline elements (K 2O, Rb), and some metal transition elements (Cu), are progressively depleted with increasing deformation. This depletion includes REE + Y, but also HFS elements (Ti, Hf, Zr, Nb) which are commonly considered as immobile elements during upper level processes. Variations in elemental ratios with deformation, e.g. decrease in LREE/MREE- HREE, Nd/Hf, Th/Sr, increase in Rb/Sr, U/Th and constant Sr/Nd, lead to propose the following order of element mobility: U ≫ Th > Sr = Nd ≫ Hf + HREE. We conclude in agreement with previous tectonic and metallogenic studies that trace element patterns across the shear zone result from circulation of oxidizing F-rich hydrothermal fluids associated with deformation. A temperature of the fluid of 470-480 °C can be deduced from the δ 18O equilibrium between quartz-muscovite pairs. Elemental fractionation induces perturbation of the Rb-Sr geochronometer. The well-defined 87Rb/ 86Sr- 87Sr/ 86Sr correlation gives an apparent age of 294 ± 19 Ma, slightly younger than the 323 ± 4 Ma age of leucogranites in this area. This apparent age is interpreted as dating event of intense deformation and fluid circulation

  1. Constraints on mantle source and interactions from He-Sr isotope variation in Italian Plio-Quaternary volcanism

    Science.gov (United States)

    Martelli, M.; Nuccio, P. M.; Stuart, F. M.; di Liberto, V.; Ellam, R. M.

    2008-02-01

    Helium isotope ratios of olivine and pyroxene phenocrysts from Plio-Quaternary volcanic rocks from southern Italy (seven Aeolian Islands, Mt. Vulture, Etna, Ustica, and Pantelleria) range from 2.3 to 7.1 Ra. Importantly, the phenocryst 3He/4He correlate well with whole rock Sr isotopic composition (0.70309-0.70711), reflecting the mixing of two sources. A significant contribution of He from crustal contamination is recorded only occasionally (e.g., pyroxenes from Vulcano). When merged with data from the Roman Comagmatic Province, a remarkably strong near-linear He-Sr isotope correlation is apparent. The general northward decrease in 3He/4He corresponds to an increase in 87Sr/86Sr (and a decrease in 143Nd/144Nd and 206Pb/204Pb) that is due to increasing metasomatic enrichment of the mantle wedge via subduction of the Ionian-Adriatic plate. Calculations based on the ingrowth of 4He in the wedge and on the 4He content of the subducting crust show that mechanisms of enrichment in radiogenic He are effective only if the wedge is strongly depleted in He relative to best estimates of the depleted mantle. This can be accommodated if the process of metasomatism by the subduction fluids depletes the mantle wedge. The 3He/4He of Pantelleria, Etna, Iblei, Ustica, Alicudi, and Filicudi basalts (7.0 ± 0.6 Ra) define the mantle composition least affected by subduction-related metasomatism. Although these volcanoes are from a variety of tectonic regimes (subduction-related, intraplate, rifting), their similarities suggest a common origin of geochemical features. Their characteristics are consistent with a HIMU-type mantle that either is younger than the Cook-Austral island end-member or has a lower 238U/204Pb.

  2. Sr isotope chemistry of the magmatism from Momchilgrad depression (Eastern Rhodopes)

    International Nuclear Information System (INIS)

    The (87Sr/86Sr)i of Zvezdel basaltic-andesite complex ranges between 0.705087 and 0.708613. Acid complexes have lower values of these ratios: Perperek trachyrhyolite - 0.69534, Ursula rhyolite - 0.70119, Sveti Ilia trachyrhyodacite - 0.70270 and Momchilgrad trachydacite - 0.70589. Considering all acid complexes the (87Sr/86Sr)i of Sveti Ilia trachyrhyodacite and Sveti Ilia trachyrhyodacite complexes are comparable with these of Zvezdel basaltic-andesite complex. The outcrops of their products associate spatially with the intermediate complexes as both acid and intermediate varieties have similar petrochemical features and trace element abundance. These complexes might have been produced by one magma reservoir of intermediate composition. Obtained (87Sr/86Sr)i values are typical of continental tectonic settings. The occurrences of Ustra rhyolite and Perperek trachyrhyolite complexes are located apart from the intermediate volcanics. The have significantly lower Sr contents, lower (87Sr/86Sr)i and specific petrochemical features and trace element distribution patterns and probably resulted from the evolution of separate and not large magma reservoirs of acid composition. Calculated (87Sr/86Sr)i for Perperek and Ustra complexes are typical of the island-arc or even mid-oceanic ridge tectonic settings. These data indirectly confirm the idea of involving both oceanic and continental crust during a process of 'continental subduction'. (authors)

  3. Sources, migration and transformation of antimony contamination in the water environment of Xikuangshan, China: Evidence from geochemical and stable isotope (S, Sr) signatures.

    Science.gov (United States)

    Wen, Bing; Zhou, Jianwei; Zhou, Aiguo; Liu, Cunfu; Xie, Lina

    2016-11-01

    The Xikuangshan (XKS) mine in central China is the largest antimony (Sb) mine in the world. The mining activity has seriously contaminated the waters in the area. To determine the sources, migration and transformation of Sb contamination, 32 samples from groundwater (aquifer water), surface water and mine water were collected for water chemistry, trace element and SSO4 and Sr stable isotope analyses. The results showed that the groundwater and surface water were in an oxidized environment. The SSO4 and Sr isotope compositions in the water indicated that dissolved Sb and SO4(2) originated from sulfide mineral (Sb2S3) oxidation, whereas radiogenic Sr may have been sourced from silicified limestone and stibnite in the Shetianqiao aquifer. Furthermore, a positive correlation between δ(34)SSO4 and δ(87)Sr values revealed that the Sr, S and Sb in the waters had a common contamination source, i.e., silicified limestone and stibnite, whereas the Sr, S and Sb in rock and ore were sourced from Proterozoic basement clastics. The analysis also indicated that the isotope composition of dissolved SO4(2-) had been influenced by slight bacterial SO4 reduction in the Magunao aquifer. Mining or rock collapse may have caused Shetianqiao aquifer water to contaminate the Magunao aquifer water via mixing. This study has demonstrated that the stable isotopes of (34)SSO4 and (87)Sr, combined with hydrochemical methods, are effective in tracking the sources, migration and transformation of Sb contamination. PMID:27341112

  4. C- and Sr-isotope stratigraphy of the São Caetano complex, Northeastern Brazil: a contribution to the study of the Meso-Neoproterozoic seawater geochemistry

    Directory of Open Access Journals (Sweden)

    Juan C. Silva

    2005-03-01

    Full Text Available C-isotope and 87Sr/86Sr values for five carbonate successions from the São Caetano Complex, northeastern Brazil, were used to constrain their depositional age and to determine large variations in the C- and Sr-isotopic composition of seawater under the framework of global tectonic events. Three C-isotope stages were identified from base to top in a composed chemostratigraphic section: (1 stage in which delta13C values vary from +2 to +3.7‰ PDB and average 3‰ PDB, (2 stage with delta13C values displaying stronger oscillations (from -2‰ to +‰ PDB, and (3 stage with an isotopic plateau with values around +3.7‰ PDB. Constant 87Sr/86Sr values (~ 0.70600 characterize C-isotope stage 1, whereas slightly fluctuating values (from 0.70600 to 0.70700 characterize C-isotope stage 2. Finally, 87Sr/86Sr values averaging 0.70600 characterize C-isotope stage 3. The C- and Sr- chemostratigraphic pathways permit to state: (a the C- and Sr-isotope secular curves registered primary fluctuations of the isotope composition of seawater during late Mesoproterozoic- early Neoproterozoic transition in the Borborema Province, and (b onset of the Cariris Velhos/Greenville cycle, widespread oceanic rifting, continental magmatic arc formation and onset of the agglutination of Rodinia supercontinent, mostly controlled the C- and Sr-isotope composition of seawater during the C-isotope stages 1, 2 and 3.Valores de isótopos de C e 87Sr/86Sr de cinco seqüências de carbonatos do Complexo São Caetano, nordeste do Brasil; foram usados para estimar a sua idade de deposição e relacionar variações da composição isotópica na água do mar com eventos tectônicos globais. Três estágios de variação de isótopos de carbono foram identificados de base para o topo numa seção quimioestratigráfica composta: (1 estágio em que delta13C varia de +2 a +3.7‰PDB (media 3‰PDB, (2 estágio no qual delta13C varia consideravelmente (de -2 a +3‰PDB e (3 est

  5. Rb, Sr and strontium isotopic composition, K/Ar age and large ion lithophile trace element abundances in rocks and glasses from the Wanapitei Lake impact structure

    International Nuclear Information System (INIS)

    Shock metamorphosed rocks and shock-produced melt glasses from the Wanapitei Lake impact structure have been examined petrographically and by electron microprobe. Eleven clasts exhibiting varying degrees of shock metamorphism and eight impact-produced glasses have been analyzed for Rb, Sr and Sr isotopic composition. Five clasts and one glass have also been analyzed for large ion lithophile (LIL) trace element abundances including Li, Rb, Sr, and Ba and the REE's. The impact event forming the Wanapitei Lake structure occurred 37 m.y. ago based on K/Ar dating of glass and glassy whole-rock samples. Rb/Sr isotopic dating failed to provide a meaningful whole-rock or internal isochron. The isotopic composition of the glasses can be explained by impact-produced mixing and melting of metasediments. Large ion lithophile trace element abundance patterns confirm the origin of the glasses by total shock melting of metasediments. (author)

  6. APPLICATION OF O-H-B-Sr ISOTOPE SYSTEMATICS TO THE EXPLORATION OF SALINIZATION AND FLUSHING IN COASTAL AQUIFERS : PRELIMINARY DATA FROM THE PIALASSA BAIONA ECOSYSTEM (ADRIATIC SEA

    Directory of Open Access Journals (Sweden)

    Riccardo Petrini

    2009-07-01

    Full Text Available O, H, B and Sr isotopes were identified from surface-waters, ground-waters and waters percolating in soils at the Pialassa Baiona lagoon and nearby inland areas. The preliminary data demonstrate the occurrence of both conservative mixtures between seawater and freshwaters and cation exchange at the salt/fresh water interface during the intrusion. The O and H isotopes indicate that the freshwater component in the binary mixing had the isotopic features of the rainwater from Apennine catchments. Coupled O-H-B isotopes also show that the major contribution of the moving seawater was confined to the deeper aquifers and some of the soil waters. The Sr isotopes highlight the role of cation exchanges when seawater flushes freshwater aquifers, and allow the recognition of the different components of the solute. Deviations from these processes as revealed by B isotopes are interpreted as the evidence of possible anthropogenic inputs.

  7. Experimental study of the Mg and Sr isotopic evolution of seawater interacting with basalt between 150 and 300 ° C.

    Science.gov (United States)

    Voigt, Martin; Pearce, Christopher R.; Oelkers, Eric H.

    2016-04-01

    The chemical exchange of material between seawater and the oceanic crust plays a major role in marine geochemical cycles [1]. Isotopic signatures provide an important means of tracing elemental transfer in hydrothermal environments, yet only a limited amount of experimental data on the extent of isotopic fractionation under these conditions is currently available. This study consequently investigated the extent of δ26/24Mg and 87Sr/86Sr isotopic variation during a seawater-basalt interaction experiments at 150, 250 and 290 ° C. A suite of closed system experiments were run for several months at each temperature under saturated water pressure, using either crystalline or glassy basalt as the starting material and a water/rock ratio of 10 or 25. Our results demonstrate that the dissolution of basaltic material in hydrothermal environments occurs at the same time as the precipitation of alteration minerals (mainly smectite and anhydrite), which is consistent with results from similar studies in the past (e.g. [2]). As expected, the rate of reaction using crystalline basalt was slower than with basaltic glass, and both sample types reacted faster at higher temperatures. The 87Sr/86Sr composition of the experimental fluids decreased from the initial seawater value (0.70916) towards the lower basaltic signature during the experiments (0.70317), demonstrating the progressive release of Sr during basalt dissolution. Magnesium was steadily removed from the fluid via the precipitation of clay minerals, with the residual fluids having progressively lighter δ26/24Mg compositions. The mean Mg isotope fractionation factor (αsolid‑solution) observed at 250 oC was 1.0005±0.0002, supporting low-temperature evidence that clay minerals preferentially incorporate isotopically heavy magnesium [3]. These experiments provide quantitative information on the extent of Mg isotopic fractionation between fluids and secondary silicate minerals in hydrothermal systems, and demonstrate

  8. Midcontinent rift volcanism in the Lake Superior region: Sr, Nd, and Pb isotopic evidence for a mantle plume origin

    Energy Technology Data Exchange (ETDEWEB)

    Nicholson, S.W. (Geological Survey, Reston, VA (USA) Univ. of Minnesota, MN (USA)); Shirey, S.B. (Carnegie Institution of Washington, DC (USA))

    1990-07-10

    Between 1091 and 1098 Ma, most of a 15- to 20-km thickness of dominantly tholeiitic basalt erupted in the Midcontinent Rift System of the Lake Superior region, North American. The Portage Lake Volcanics in Michigan, which are the youngest MRS flood basalts, fall into distinctly high- and low-TiO{sub 2} types having different liquid lines of descent. Incompatible trace elements in both types of tholeiites are enriched compared to depleted or primitive mantle (La/Yb = 4.3-5.3; Th/Ta = 2.12-2.16; Zr/Y = 4.3-4.4), and both basalt types are isotopically indistinguishable. Sr, Nd, and Pb isotopic compositions of the Portage Lake tholeiites have {sup 87}Sr/{sup 86}Sr{sub i} {approx}0.7038, {epsilon}{sub Nd(1095 Ma)} {approx}0 {plus minus} 2, and {mu}{sub 1} {approx}8.2. Model ages with respect to a depleted mantle source (T{sub DM}) average about 1950-2100 Ma. Portage Lake rhyolits fall into two groups. Type I rhyolites have Nd and Pb isotopic characteristics ({epsilon}{sub Nd(1095 Ma)} {approx}0 to {minus}4.7; {mu}{sub 1} {approx}8.2-7.8) consistent with contamination of tholeiitic rocks by 5-10% Archean crust. The one type II rhyolite analyzed has Nd and Pb isotopic compositions ({epsilon}{sub Nd(1095 Ma)} {approx}{minus}13 to {minus}16; {mu}{sub 1} {approx}7.6-7.7) which are consistent with partial melting of Archean crust. Early Proterozoic crust was not a major contaminant of MRS rocks in the Lake Superior region. Most reported Nd and Pb isotopic compositions of MRS tholeiites from the main stage of volcanism in the Lake Superior region and of the Duluth Complex are comparable to the Nd and Pb isotopic data for Portage lake tholeiites. The isotopic enrichment of the MRS source compared to depleted mantle is striking and must have occurred at least 700 m.y. before 1100 Ma.

  9. Chemical and U-Sr isotopic variations in stream and source waters of the Strengbach watershed (Vosges mountains, France)

    Science.gov (United States)

    Pierret, M. C.; Stille, P.; Prunier, J.; Viville, D.; Chabaux, F.

    2014-10-01

    This is the first comprehensive study dealing with major and trace element data as well as 87Sr/86Sr isotope and (234U/238U) activity ratios (AR) determined on the totality of springs and brooks of the Strengbach catchment. It shows that the small and more or less monolithic catchment drains different sources and streamlets with very different isotopic and geochemical signatures. Different parameters control the diversity of the source characteristics. Of importance is especially the hydrothermal overprint of the granitic bedrock, which was stronger for the granite from the northern slope; also significant are the different meteoric alteration processes of the bedrock causing the formation of 0.5 to 9 m thick saprolite and above the formation of an up to 1m thick soil system. These processes mainly account for springs and brooks from the northern slope having higher Ca / Na, Mg / Na, and Sr / Na ratios, but lower 87Sr/86Sr isotopic ratios than those from the southern slope. The chemical compositions of the source waters in the Strengbach catchment are only to a small extent the result of alteration of primary bedrock minerals, and rather reflect dissolution/precipitation processes of secondary mineral phases like clay minerals. The (234U/238U) AR, however, are decoupled from the 87Sr/86Sr isotope system, and reflect to some extent the level of altitude of the source and, thus, the degree of alteration of the bedrock. The sources emerging at high altitudes have circulated through already weathered materials (saprolite and fractured bedrock depleted in 234U), implying (234U/238U) AR below 1, which is uncommon for surface waters. Preferential flow paths along constant fractures in the bedrocks might explain the - over time - homogeneous U AR of the different spring waters. However, the geochemical and isotopic variations of stream waters at the outlet of the catchment are controlled by variable contributions of different springs, depending on the hydrological

  10. APPLICATION OF O-H-B-Sr ISOTOPE SYSTEMATICS TO THE EXPLORATION OF SALINIZATION AND FLUSHING IN COASTAL AQUIFERS : PRELIMINARY DATA FROM THE PIALASSA BAIONA ECOSYSTEM (ADRIATIC SEA)

    OpenAIRE

    Riccardo Petrini; Maddalena Pennisi; Alessandra Adorni Braccesi; Barbara Stenni; Onelio Flora; Umberto Aviani

    2009-01-01

    O, H, B and Sr isotopes were identified from surface-waters, ground-waters and waters percolating in soils at the Pialassa Baiona lagoon and nearby inland areas. The preliminary data demonstrate the occurrence of both conservative mixtures between seawater and freshwaters and cation exchange at the salt/fresh water interface during the intrusion. The O and H isotopes indicate that the freshwater component in the binary mixing had the isotopic features of the rainwater from Apennine catchments...

  11. Sr-Nd-Pb Isotope Geochemistry of Lesser Qinling%小秦岭碳酸岩的Sr-Nd-Pb同位素地球化学

    Institute of Scientific and Technical Information of China (English)

    王林均; 许成; 吴敏; 宋文磊; 唐红峰

    2012-01-01

    The Lesser Qinling carbonatite is located at the southern margin of North China craton.The Sr,Nd isotopic characteristics are close to the EM1 mantle member [(87Sr/86Sr)i =0.70495~0.70552;εNd =-10.1~4.6],but with low Sr and Nd compared to EM1.The Pb isotopic characteristics of the carbonate rocks are in the range of southern Qinling Mountains,completely different from the North China plate.This implies that the lower crust or mantle of the southern margin of the North China Craton has been mixed with the lower crust of South Qinling.So the carbonatites formed at the stage of extension after collision in the Qinling orogeric belt.This paper also argues that the Triassic granitoids formed under an extension background and were involved in mantle materials from Qinling Orogenic belt.%小秦岭碳酸岩位于华北板块南缘,其(87Sr/86Sr)i与εNd值分别介于0.70495~0.70552和-10.1~4.6之间,紧靠EM1地幔端元,但相对EM1具有低Sr和低Nd特征。Pb同位素与华北板块南缘完全不同,而是落在了南秦岭下地壳范围之内,这表明华北板块南缘下地壳或地幔已经受到南秦岭地壳物质俯冲置换的影响,即在晚三叠纪时期,秦岭地区的碰撞造山作用可能已经结束,转入伸展拉张的构造环境。并进一步论述了秦岭地区三叠纪花岗岩是在深部拉张的构造环境下形成以及具有幔源物质参与的特征。

  12. Magma Mixing for the Origin of the Granites. Geochemistry, Sr-Nd Isotopic, Zircon U-Pb Dating and Hf Isotopic Evidences from the Triassic Mishuling Monzonitic Granite and Its Enclaves, Qinling Orogen (Central China)

    Institute of Scientific and Technical Information of China (English)

    QIN Jiang-feng; LAI Shao-cong; DIWU Chun-rong; JU Yin-juan; LI Yong-fei

    2008-01-01

    @@ Major and trace element, whole rock Sr-Nd isotope, mineral chemistry, zircon U-Pb and Hf isotope compositions are reported for a suite of I-type monzogranite and its marie microgranular enclaves from the Triassic (210±2 Ma) Mishuling pluton, Qinling orogen, central China, with the aim of investigating the sources and petrogenesis of I-type granites.

  13. Sr and Nd isotopic evidence for petrogenesis of mid-Tertiary felsic volcanism in the mineral district of Zacatecas, Zac. (Sierra Madre Occidental), Mexico

    International Nuclear Information System (INIS)

    Twelve samples of mid-Tertiary felsic volcanic rocks from Zacatecas and San Luis Potosi (both belonging to the Sierra Madre Occidental) and one sample of Lower Tertiary porphyritic andesite from Zacatecas are analyzed for 87Sr/86Sr, K, Rb, and Sr. Eight selected samples are also analyzed for 143Nd/144Nd. A linear regression of the present-day 87Sr/86Sr and 87Rb/86Sr of the felsic volcanic rocks in Zacatecas gives an approximate date of 30 +- 8 Ma. The initial 87Sr/86Sr ratios are high and widely distributed (from 0.705 to 0.712 or higher) whereas the initial 143Nd/144Nd ratios are somewhat low and show a narrow range (0.5125-0.5127). The available isotopic and trace-element data are best explained in terms of a binary mixing model in which the magmas derived from a slightly depleted-mantle fractionate and mix with varying proportions of the overlying middle/upper continental crust and undergo further shallow-level fractional crystallization before eruption. This model is also compatible with the trace-element and Sr isotopic data published from other areas of the Sierra Madre Occidental for which a purely mantle origin has been proposed. (orig.)

  14. Carbonate verse silicate Sr isotope in lake sediments and its response to Little Ice Age

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The 87Sr/86Sr ratios of silicate (acid-insoluble, AI) and carbonate (acid-soluble, AS) of the lake sediments from the Daihai Lake, Inner Mongolia, since the last 500 years are measured respectively, indicating that chemical weathering of silicate minerals was in an early stage since the Little Ice Age within the Daihai watershed by combination with mineral constitute, Rb/Sr ratio and CaCO3 content in the sediments. During the Little Ice Age maximum, an evident peak in the 87Sr/86Sr ratios of both silicate and carbonate in sediments suggests that a cold climate condition is unfavorable to dissolving radiogenic strontium from silicate minerals. Meanwhile, the variation of 87Sr/86Sr ratios of silicate and carbonate also reflects a projected warming climate favorable to intensifying chemical weathering after the Little Ice Age. Consequently, the 87Sr/86Sr ratio of both silicate and carbonate in inland lake sediments can be used as an effective proxy of the past climate in single watershed.

  15. Accurate measurement of neodymium isotopic composition using Neptune MC-ICP-MS

    Institute of Scientific and Technical Information of China (English)

    Yueheng YANG; Hongfu ZHANG; Liewen XIE; Fuyuan WU

    2008-01-01

    This paper reports the measurement of the Neodymium isotopic composition by Neptune Multiple Collector Inductively Coupled Plasma Mass Spectrometry (MC-ICP-MS) over the last two years. Although there is concomitant Cerium in the chemical separation process, this has no significant influence on the Neodymium analysis. As for the sample containing small amounts of Samarium (Sm/Nd<0.04), direct calibration for isobaric interference and mass discrimina-tion by the exponential law can be obtained by assuming that Samarium mass discrimination is the same as that of Neodymium. Geological samples after traditional chemi-cal separation were measured by Neptune MC-ICP-MS and Thermal Ionization Mass Spectrometry (TIMS) respectively. The results show that Neptune MC-ICP-MS can measure Neodymium isotopic composition as precisely the TIMS does and is even more effective and less time-consuming than the TIMS Method.

  16. A summary of Rb-Sr isotope studies in the Archean Hopedale Block and the adjacent proterozoic Makkovik subprovince, Labrador

    International Nuclear Information System (INIS)

    Rb-Sr isotope study of thirteen whole-rock suites of Archean and Proterozoic rocks from Hopedale block and Makkovik Subprovince shows that the crustal history began about 3115 Ma ago. We tentatively recognize younger crustal segments that formed 2920 Ma ago, from which Kanairktok intrusives were derived at 2832 +- 178 Ma. In Makkovik Subprovince the Island Harbour granites range in age from 1843 +- 90 to 1794 +- 71 Ma. These ages overlap with the 1847 +-87 Ma age for Kanairktok shear zone mylonites. The Island Harbour granodiorites from inland localities to the southwest are contaminated with Archean rocks in Makkovik Subprovince and their initial 87Sr/86 ratios imply a crustal contribution to their source. In contrast, the Island Harbour granites of Striped Island were derived from a mantle source. The sills of Striped Island are 1635 +- 47 Ma old. An undeformed northeast trending Kikkertavak dolerite dyke from Hopedale block is 1206 +- 120 Ma

  17. Mass measurements on neutron-deficient Sr and neutron-rich Sn isotopes with the ISOLTRAP mass spectrometer

    CERN Document Server

    Sikler, G; Beck, D; Blaum, K; Bollen, G; Herfurth, F; Kellerbauer, A G; Kluge, H J; Lunney, M D; Oinonen, M; Scheidenberger, C; Schwarz, S; Szerypo, J

    2005-01-01

    The atomic masses of $^{76,77,80,81,86,88}$Sr and $^{124,129,130,131,132}$Sn were measured by means of the Penning trap mass spectrometer ISOLTRAP at ISOLDE/CERN. $^{76}$Sr is now the heaviest N=Z nucleus for which the mass is measured to a precision better than 35 keV. For the tin isotopes in the close vicinity of the doubly magic nucleus $^{132}$Sn, mass uncertainties below 20 keV were achieved. An atomic mass evaluation was carried out taking other experimental mass values into account by performing a least-squares adjustment. Some discrepancies between older experimental values and the ones reported here emerged and were resolved. The results of the new adjustment and their impact will be presented.

  18. B, Sr, O and H Isotopic Compositions of Formation Waters from the Bachu Bulge in the Tarim Basin

    Institute of Scientific and Technical Information of China (English)

    CAI Chunfang; PENG Licai; MEI Bowen; XIAO Yingkai

    2006-01-01

    In order to elucidate the origin and migration of basinal brines in the Bachu Bulge, Tarim Basin, we have carried out analyses on chemical composition, and boron, hydrogen and oxygen isotopes of formation waters together with the XRD of clay minerals from the Paleozoic strata. The waters show Ca, B, Li and Sr enrichment and SO4 depletion in the Carboniferous and Ordovician and K enrichment in part of the Ordovician relative to seawater. The relationship between δD and δ18O shows that all the data of the waters decline towards the Global Meteoric Water Line with the intersection of them close to the present-day local meteoric water, suggesting that modern meteoric water has mixed with evaporated seawater. The 87Sr/86Sr ratios range from 0.7090 to 0.7011, significantly higher than those of the contemporary seawater. The δ11B values range from +19.7 to +32.3‰, showing a decrease with the depth and B concentrations. The results suggest that isotopically distinct B and Sr were derived from external sources. However, since the percentages of illite are shown to increase with depth among clay minerals in the study area, i.e., illite is due to precipitation rather than leaching during deeper burial, it is unlikely for illite to have contributed a significant amount of B to the waters. Thus, B with low δ11B values is interpreted to have been added mainly from thermal degradation of kerogen or the basalts in the Cambrian and Lower Ordovician.

  19. The Late Devonian Frasnian-Famennian (F/F) biotic crisis: Insights from δ13C carb, δ13C org and 87Sr / 86Sr isotopic systematics

    Science.gov (United States)

    Chen, Daizhao; Qing, Hairuo; Li, Renwei

    2005-06-01

    A severe biotic crisis occurred during the Late Devonian Frasnian-Famennian (F/F) transition (± 367 Myr). Here we present δ13C carb, δ13C org and 87Sr / 86Sr isotopic systematics, from identical samples of two sections across F/F boundary in South China, which directly demonstrate large and frequent climatic fluctuations (˜200 kyr) from warming to cooling during the F/F transition. These climate fluctuations are interpreted to have been induced initially by increased volcanic outgassing, and subsequent enhanced chemical weathering linked to the rapid expansion of vascular plants on land, which would have increased riverine delivery to oceans and primary bioproductivity, and subsequent burial of organic matter, thereby resulting in climate cooling. Such large and frequent climatic fluctuations, together with volcanic-induced increases in nutrient (e.g., biolimiting Fe), toxin (sulfide) and anoxic water supply, and subsequent enhanced riverine fluxes and microbial bloom, were likely responsible for the stepwise faunal demise of F/F biotic crisis.

  20. Definition of the optimal terms isotope 82Sr obtaining on cyclotrons U-240

    International Nuclear Information System (INIS)

    Analysis of the various nuclear reactions for the production of radionuclide 82Sr was performed and optimum process for the production of this radionuclide was determined. Proton beam energy range for minimizing 85Sr impurity was also determined. The thickness of the RbCl target was calculated

  1. Hydrocarbon filling history and reservoir continuity of oil fields evaluated using {sup 87}Sr/{sup 86}Sr isotope ratio variations in formation water, with examples from the North Sea

    Energy Technology Data Exchange (ETDEWEB)

    Mearns, E.W.; McBride, J.J. [Isotopic Analytical Services Ltd., Aberdeen (United Kingdom)

    1999-02-01

    This paper describes how {sup 87}Sr/{sup 86}Sr ratios in formation waters are used to evaluate compartmentalisation of hydrocarbon reservoirs. Strontium Isotope Residual Salt Analysis (SrRSA) of core samples provides a means of measuring {sup 87}Sr/{sup 86}Sr ratios in formation water from hydrocarbon columns and aquifers. Smooth SrRSA profiles suggest progressive, uninterrupted, filling and the absence of sealed barriers, while a step change in a profile normally suggests a barrier sealed up-dip from the well penetration. Inferences about lateral connectivity are made by comparing SrRSA profiles from neighbouring wells at TVD. Profiles that are superimposed when plotted at TVD suggest the well sections share a common filling history and lie in the same flow unit. Neighbouring SrRSA profiles that are not superimposed normally suggest segmented compartmentalisation of the reservoir. Post-fill structural tilting of reservoirs and hydrodynamism synchronous with filling are processes which complicate data interpretation. Drilling mud contamination of core water is the most serious technical limitation of the SrRSA technique. (Author)

  2. Monitoring the interaction of hydraulic fracturing fluid with Marcellus Shale using Sr isotopes: a comparison of laboratory experiments with field scale observations (Invited)

    Science.gov (United States)

    Wall, A. J.; Hakala, A.; Marcon, V.; Joseph, C.

    2013-12-01

    Strontium isotopes have the potential to be an effective tool for differentiating Marcellus Shale derived-fluids from other sources in surface and ground waters (Chapman et al. 2012, doi: 10.1021/es204005g). Water that is co-produced during gas extraction is likely influenced by fluid/rock interactions during hydraulic fracturing (HF) and monitoring changes in Sr isotope ratios can provide insight into reactions occurring within the shale formation. However, questions persist as to what controls the Sr isotopic composition of Marcellus Shale fluids, especially during HF. Here we compare laboratory experiments, simulating the dissolution of the Marcellus Shale during HF, with a time-series of water samples taken from a Marcellus Shale gas wells after HF has occurred. For the laboratory experiments, a core sample of Marcellus Shale from Greene County, PA was crushed and placed into a high P and T reaction vessel. Solutions were added in two different experiments: one with synthetic brine, and another using brine+HF fluid. The HF fluid was made up of components listed on fracfocus.org. Experiments were run for ~16 days at 27.5 MPa and 130oC. Aqueous samples were periodically removed for analysis and Sr isotope ratios were measured by MC-ICP-MS. Using just brine, the pH of the solution decreased from 7.6 to 5.3 after 24 hrs, then reached a steady state at ~6.1. Sr/Ca molar ratios in the fluid started at 2.3 after 24 hours and decreased to 1.8 over ~16 days. During this time only 6% of the total inorganic carbon (TIC) dissolved from the shale. The ɛSr values started at +43.2 and decreased to +42.4. In the experiment using brine+HF fluid, the pH started at 1.8 and rose slowly to a steady value of 5.6 by day 6. The Sr and Ca concentrations were higher than the brine experiment, but the Sr/Ca ratios remained lower at ~0.3 through the experiment. The increased Ca release, as well as the dissolution of over 60% of the TIC, suggests the dissolution of a carbonate mineral

  3. Sr-Nd-Hf-Pb isotopic constraints on the origin of silicic lavas in the northern Cascade Arc

    Science.gov (United States)

    Martindale, M.; Mullen, E.; Weis, D.

    2015-12-01

    The Cascade Arc is the type-locality for a 'hot' subduction zone, where the downgoing slab is young and subduction is relatively slow; a unique setting for studying the controls on silicic (>56 wt% SiO2) magma genesis [1,2]. We present high precision Sr-Nd-Hf-Pb isotopic and trace element data for silicic lavas and country rocks from the major centres of the Garibaldi Volcanic Belt (GVB) in British Columbia, which are hosted by the Mesozoic Coast Plutonic Complex and accreted Coast Belt terranes. In isotopic plots, the silicic GVB lavas define mixing curves between northern Cascadia Basin sediment [3] and Juan de Fuca MORB. The silicic GVB lavas have lower ɛNd, and higher ɛHf, 87Sr/86Sr, 208Pb/204Pb and 207Pb/204Pb for a given 206Pb/204Pb than co-existing alkalic mafic lavas [2,4] which define a separate isotopic cluster. The alkalic mafic lavas have OIB-like trace element compositions [2,4], but the silicic lavas are calc-alkaline with a typical 'arc' trace element signature. Geochemical systematics suggest that a mafic, isotopically 'depleted' contaminant may be affecting the composition of GVB silicic lavas. However, modelling indicates that slab melts do not constitute a major component of the lavas despite high slab temperatures. Geochemical models also rule out the accreted Coast Belt terranes as an assimilant. However, AFC modelling using 147 Ma Cloudburst quartz diorite [5] as the assimilant can explain both the trace element and isotopic compositional range displayed by GVB silicic magmas, consistent with the Coast Plutonic Complex as a major component of the deep crust in this region. Crustal assimilation would have partially overprinted any alkalic mantle-derived signature of parental magmas, while imparting a calc-alkaline arc signature to resulting silicic magmas. [1] Green & Harry (1999) EPSL, 171; [2] Mullen & Weis (2013) G3, 14; [3] Carpentier et al. (2014) Chem Geol, 382; [4] Mullen & Weis (2015) EPSL, 414; [5] Friedman & Armstrong (1995) GSA

  4. New Nd-Sr isotope-geochemical research of the paleoproterozoic PGE-bearing Monchetundra massif rocks (the Fennoscandian Shield

    Directory of Open Access Journals (Sweden)

    Kunakkuzin E.L.

    2015-06-01

    Full Text Available This paper presents results of Nd-Sr research for mafic rocks from the PGE-bearing Monchetundra massif, the Main Ridge. According to the new isotopic data mafic rocks of the massif different in age are characterized by various isotopic and geochemical characteristics. The oldest rocks of the massif (2520 Ma show a wide range of εNd(T values between +0.02 and –2.23 and Mezo- to Paleo-Archean TDM ages. Trachytoid gabbronorites (2500 Ma have εNd(T values in the range of –1.70 to +1.42 and TDM ages of 2.7 Ga to 3.5 Ga. The εNd(T values for massive gabbronorites vary between –3.38 and +2.08, and TDM ages for them are in the range from 2.7 Ga to 3.4 Ga. Segregations of gabbro-pegmatites (2450 Ma are spatially and genetically associated with massive gabbronorites and have similar isotopic and geochemical characteristics. Gabbros with high positive values εNd(T of +1.42 to +2.08 as well as TDM close to 2.7 Ga appear to be derived from a depleted mantle source. In general the Nd-Sr isotopic and geochemical data indicate that the main varieties of Monchetundra rocks have formed from mantle source enriched in large ion lithophile elements. The most likely reason of values scatter is evolution of the mantle source during the plume-lithosphere interaction

  5. Clinopyroxene-host disequilibrium (Sr-Nd-Pb isotope systematics) in ultra-potassic magmas from East-African Rift: Implications for magma mixing and source heterogeneity

    Science.gov (United States)

    Muravyeva, Natalya; Belyatsky, Boris; Senin, Valeriy

    2014-05-01

    Nd, Pb and Sr isotope ratios have been determined for kamafugite lava and clinopyroxene and phlogopite phenocrysts from Toro-Ankole and Virunga volcanic fields of the East African Rift. The whole rock Sr - Nd isotopic signatures of kamafugites (87Sr/86Sr: 0.70463 - 0.70536; 143Nd/144Nd: 0.51249 - 0.51255) suggest derivation from an EM1-type mantle source. In contrast, Pb isotopic compositions of the same samples (206Pb/204Pb: 19.00 - 19.57; 207Pb/204Pb: 15.69 - 15.74; 208Pb/204Pb: 39.30 - 40.26) reveal a similarity to EM2-type mantle. New Nd, Pb and Sr isotopic data for clinopyroxene (87Sr/86Sr: 0.70473 - 0.70503; 143Nd/144Nd: 0.51250 - 0.51254; 206Pb/204Pb: 18.04 - 18.17; 207Pb/204Pb: 15.58 - 15.60; 208Pb/204Pb: 38.09 - 38.23) suggest derivation from an EM1-like source, and indicate Sr and Pb isotope disequilibrium between clinopyroxene and corresponding host rock. Moreover, clinopyroxenes demonstrating a greater degree of isotopic disequilibrium with their host rock are more sodic in composition. The isotopic disequilibrium is corroborated by the presence of chemical zoning within clinopyroxene, which suggests rapid magma ascent rates preventing melt homogenization. The Pb isotopic ratios for both mineral and corresponding whole rock, together with published data on East African rift-related alkaline centers, define a trend interpreted to represent a mixing line for melts derived from sources such as EM1 and as HIMU. The similar isotopic compositions for clinopyroxene from the different volcanic rocks within the East African Rift suggest the existence of a common, older mantle source for their parental melts. The origin of these melts can be attributed to an enrichment event ~ 400-500 Ma, i.e., significantly prior the younger (Quaternary) ultrapotassic magmatism. Our preferred interpretation for the results reported here involves the mixing of the melts derived from EM1- and HIMU-like sources, which were rapidly transported to the Earth's surface. The primary

  6. Pb-Sr-Nd isotopes in surficial materials at the Pebble Porphyry Cu-Au-Mo Deposit, Southwestern Alaska: can the mineralizing fingerprint be detected through cover?

    Science.gov (United States)

    Ayuso, Robert A.; Kelley, Karen D.; Eppinger, Robert G.; Forni, Francesca

    2013-01-01

    The Cretaceous Pebble porphyry Cu-Au-Mo deposit is covered by tundra and glacigenic sediments. Pb-Sr-Nd measurements were done on sediments and soils to establish baseline conditions prior to the onset of mining operations and contribute to the development of exploration methods for concealed base metal deposits of this type. Pebble rocks have a moderate range for 206Pb/204Pb = 18.574 to 18.874, 207Pb/204Pb = 15.484 to 15.526, and 208,Pb/204Pb = 38.053 to 38.266. Mineralized granodiorite shows a modest spread in 87Sr/86Sr (0.704354–0.707621) and 143Nd/144Nd (0.512639–0.512750). Age-corrected (89 Ma) values for the granodiorite yield relatively unradiogenic Pb (e.g., 207Pb/204Pb 87Sr/86Sr, and positive values of ɛNd (1.00–4.52) that attest to a major contribution of mantle-derived source rocks. Pond sediments and soils have similar Pb isotope signatures and 87Sr/86Sr and 143Nd/144Nd values that resemble the mineralized granodiorites. Glacial events have obscured the recognition of isotope signatures of mineralized rocks in the sediments and soils. Baseline radiogenic isotope compositions, prior to the onset of mining operations, reflect natural erosion, transport and deposition of heterogeneous till sheets that included debris from barren rocks, mineralized granodiorite and sulfides from the Pebble deposit, and other country rocks that pre- and postdate the mineralization events. Isotopic variations suggest that natural weathering of the deposit is generally reflected in these surficial materials. The isotope data provide geochemical constraints to glimpse through the extensive cover and together with other geochemical observations provide a vector to concealed mineralized rocks genetically linked with the Pebble deposit.

  7. Trace element and Sr and Nd isotope geochemistry of peridotite xenoliths from the Eifel (West Germany) and their bearing on the evolution of the subcontinental lithosphere

    Energy Technology Data Exchange (ETDEWEB)

    Stosch, H.G.; Lugmair, G.W.

    1986-11-01

    Peridotite xenoliths from the Eifel can be divided into incompatible element-depleted and -enriched members. The depleted group is restricted to dry lherzolites whereas the enriched group encompasses dry harzburgites, dry websterite and amphibole and/or phlogopite-bearing peridotites. Isotopically the depleted group is very diverse with /sup 143/Nd//sup 144/Nd ranging from proportional to 0.51302 to 0.51355 and /sup 87/Sr//sup 86/Sr from proportional to 0.7041 to 0.7019, thus occupying a field larger than expected for oceanic-type subcontinental mantle. These xenoliths are derived from a mantle which appears to have diverged from a bulk-earth Nd and Sr isotopic evolution path proportional to 2 Ga ago as a consequence of partial melting. The combination of high /sup 143/Nd//sup 144/Nd with high /sup 87/Sr//sup 86/Sr in some members of depleted-xenoliths suite is likely to be the result of incipient reaction with incompatible element-enriched fluids in the mantle. In the enriched group such reactions have proceeded further and erased any pre-enriched isotope memory resulting in a smaller isotopic diversity (/sup 143/Nd//sup 144/Nd proportional to 0.51256-0.51273, /sup 87/Sr//sup 86/Sr proportional to 0.7044-0.7032). An evaluation of Sm-Hf and Yb-Hf relationships suggests that the amphibole-bearing lherzolites and harzburgites acquired their high enrichment of light rare earth elements by fluid infiltration into previously depleted peridotite rather than by silicate melt-induced metasomatism. Upper mantle composed of such metasomatized peridotites does not represent a potential source for the basanites and nephelinites from the Eifel. The isotopic and chemcial diversity of the subcontinental lithospheric part of the mantle may result from it having remained isolated from the convecting mantle for times >1 Ga.

  8. Ion microprobe Sr isotope analysis of carbonates with about 5 {mu}m spatial resolution: An example from an ayu otolith

    Energy Technology Data Exchange (ETDEWEB)

    Sano, Yuji [Center for Advanced Marine Research, Ocean Research Institute, University of Tokyo, Nakano-ku, Tokyo 164-8639 (Japan)], E-mail: ysano@ori.u-tokyo.ac.jp; Shirai, Kotaro [International Coastal Research Center, Ocean Research Institute, University of Tokyo, Otsuchi, Iwate 028-1102 (Japan); Takahata, Naoto; Amakawa, Hiroshi [Center for Advanced Marine Research, Ocean Research Institute, University of Tokyo, Nakano-ku, Tokyo 164-8639 (Japan); Otake, Tsuguo [International Coastal Research Center, Ocean Research Institute, University of Tokyo, Otsuchi, Iwate 028-1102 (Japan)

    2008-08-15

    A high lateral resolution secondary ion mass spectrometer (NanoSIMS NS50 ion microprobe) has been used to measure {sup 87}Sr/{sup 86}Sr ratios in natural CaCO{sub 3} samples. A {approx}2 nA O{sup -} primary beam was used to sputter a 5-7-{mu}m diameter crater on the sample surface and secondary positive ions were extracted for mass analysis using an accelerating voltage of 8 kV and a Mattauch-Herzog geometry. The multi-collector system was adjusted to detect {sup 43}Ca{sup +} (by a detector EM2), {sup 80}Ca{sub 2}{sup +} (EM3), {sup 86}Sr{sup +} (EM4), and {sup 87}Sr{sup +} (EM4b) ions at the same time. Then the magnetic field was scanned for the EM4 to detect {sup 85}Rb{sup +}, {sup 86}Sr{sup +} and {sup 87}Sr{sup +}, while the EM4b can measure {sup 86}Sr{sup +}, {sup 87}Sr{sup +} and {sup 88}Sr{sup +}, respectively. A mass resolution of 3600 at 10% peak height was attained with a flat peak top, while the sensitivity of Sr was about 10 cps/nA/ppm. An aragonite sample (coral skeleton standard; JCp-1) was used as a reference for Sr isotope ratio calibration. Repeated analyses of the JCp-1 show that the {sup 87}Sr/{sup 86}Sr ratio agrees well with the seawater signature within a precision of 0.3 per mille at 2{sigma}, after the series of corrections such as the Ca dimer, {sup 87}Rb, and a mass bias estimated by the {sup 88}Sr/{sup 86}Sr ratio. The method was applied to an otolith (ear-stone) from ayu (Plecoglossus altivelis altivelis) collected from the Yodo river, Japan. Although experimental errors are relatively large, up to 3 per mille at 2{sigma}, the ratios of the core region are higher than the seawater signature while more distal values agree well with seawater. The very outermost part again shows the relatively higher {sup 87}Sr/{sup 86}Sr ratios. The spatial variation of {sup 87}Sr/{sup 86}Sr ratios was consistent with amphidromous migration of the fish, namely, born in the lake and grown in the coastal sea and finally collected in a river.

  9. Ca, Sr, Mo and U isotopes evidence ocean acidification and deoxygenation during the Late Permian mass extinction

    Science.gov (United States)

    Silva-Tamayo, Juan Carlos; Payne, Jon; Wignall, Paul; Newton, Rob; Eisenhauer, Anton; Weyer, Stenfan; Neubert, Nadja; Lau, Kim; Maher, Kate; Paytan, Adina; Lehrmann, Dan; Altiner, Demir; Yu, Meiyi

    2014-05-01

    The most catastrophic extinction event in the history of animal life occurred at the end of the Permian Period, ca. 252 Mya. Ocean acidification and global oceanic euxinia have each been proposed as causes of this biotic crisis, but the magnitude and timing of change in global ocean chemistry remains poorly constrained. Here we use multiple isotope systems - Ca, Sr, Mo and U - measured from well dated Upper Permian- Lower Triassic sedimentary sections to better constrain the magnitude and timing of change in ocean chemistry and the effects of ocean acidification and de-oxygenation through this interval. All the investigated carbonate successions (Turkey, Italy and China) exhibit decreasing δ44/40Ca compositions, from ~-1.4‰ to -2.0‰ in the interval preceding the main extinction. These values remain low during most of the Griesbachian, to finally return to -1.4‰ in the middle Dienerian. The limestone succession from southern Turkey also displays a major decrease in the δ88/86Sr values from 0.45‰ to 0.3‰ before the extinction. These values remain low during the Griesbachian and finally increase to 0.55‰ by the middle Dienerian. The paired negative anomalies on the carbonate δ44/40Ca and δ88/86Sr suggest a decrease in the carbonate precipitation and thus an episode of ocean acidification coincident with the major biotic crisis. The Mo and U isotope records also exhibit significant rapid negative anomalies at the onset of the main extinction interval, suggesting rapid expansion of anoxic and euxinic marine bottom waters during the extinction interval. The rapidity of the isotope excursions in Mo and U suggests substantially reduced residence times of these elements in seawater relative to the modern, consistent with expectations for a time of widespread anoxia. The large C-isotope variability within Lower Triassic rocks, which is similar to that of the Lower-Middle Cambrian, may reflect biologically controlled perturbations of the oceanic carbon cycle

  10. A model that helps explain Sr-isotope disequilibrium between feldspar phenocrysts and melt in large-volume silicic magma systems

    Science.gov (United States)

    Duffield, Wendell A.; Ruiz, Joaquin

    1998-12-01

    Feldspar phenocrysts of silicic volcanic rocks are commonly in Sr-isotopic disequilibrium with groundmass. In some cases the feldspar is more radiogenic, and in others it is less radiogenic. Several explanations have been published previously, but none of these is able to accommodate both senses of disequilibrium. We present a model by which either more- or less-radiogenic feldspar (or even both within a single eruptive unit) can originate. The model requires a magma body open to interaction with biotite- and feldspar-bearing wall rock. Magma is incrementally contaminated as wall rock melts incongruently. Biotite preferentially melts first, followed by feldspar. Such melting behavior, which is supported by both field and experimental studies, first contaminates magma with a relatively radiogenic addition, followed by a less-radiogenic addition. Feldspar phenocrysts lag behind melt (groundmass of volcanic rock) in incorporating the influx of contaminant, thus resulting in Sr-isotopic disequilibrium between the crystals and melt. The sense of disequilibrium recorded in a volcanic rock depends on when eruption quenches the contamination process. This model is testable by isotopic fingerprinting of individual feldspar crystals. For a given set of geologic boundary conditions, specific core-to-rim Sr-isotopic profiles are expectable. Moreover, phenocrysts that nucleate at different times during the contamination process should record different and predictable parts of the history. Initial results of Sr-isotopic fingerprinting of sanidine phenocrysts from the Taylor Creek Rhyolite are consistent with the model. More tests of the model are desirable.

  11. Multiple sources for the origin of granites: Geochemical and Nd/Sr isotopic evidence from the Gudaoling granite and its mafic enclaves, northeast China

    Science.gov (United States)

    Yang, Jin-Hui; Wu, Fu-Yuan; Chung, Sun-Lin; Wilde, Simon A.; Chu, Mei-Fei

    2004-11-01

    Geochemical and Sr- and Nd-isotopic data have been determined for mafic to intermediate microgranular enclaves and host granitoids from the Early Cretaceous Gudaoling batholith in the Liaodong Peninsula, NE China. The rocks include monzogranite, porphyric granodiorite and quartz diorite. Monzogranites have relatively high 87Rb/ 86Sr ratios (0.672-0.853), low initial 87Sr/ 86Sr ratios (0.7052-0.7086) and ɛ Nd(t) values (-18.5 to -20.9) indicating that they were mainly derived from a newly underplated crustal source with a short crustal residence time. Quartz diorites have high initial 87Sr/ 86Sr ratios (0.7118-0.7120) and negative ɛ Nd(t) values (-13.2 to -18.1) coupled with high Al 2O 3 and MgO contents, indicating they were derived from enriched lithospheric mantle with contributions of radiogenic Sr from plagioclase-rich metagreywackes or meta-igneous rocks, i.e., ancient lower crust. Two groups of enclaves with igneous textures and abundant acicular apatites are distinguished: dioritic enclaves and biotite monzonitic enclaves. Dioritic enclaves have low Al 2O 3 (13.5-16.4 wt%) and high MgO (Mg# = ˜72.3) concentrations, low initial 87Sr/ 86Sr ratios (0.7058-0.7073) and negative ɛ Nd(t) values (˜-7.2), and are enriched in LILEs and LREEs and depleted in HFSEs, suggesting they were derived from an enriched lithospheric mantle source. Biotite monzonitic enclaves have Sr and Nd isotopic compositions similar to the monzogranites, indicating they were crystal cumulates of the parental magmas of these monzogranites. Granodiorites have transitional geochemistry and Nd- and Sr-isotopic compositions, intermediate between the monzogranites, quartz diorites and the enclaves. Geochemical and Sr- and Nd-isotopic compositions rule-out simple crystal-liquid fractionation or restite unmixing as the major genetic link between enclaves and host rocks. Instead, magma mixing of mafic mantle-derived and juvenile crustal-derived magmas, coupled with crystal fractionation and

  12. Rare earth elements and (87)Sr/(86)Sr isotopic characterization of Indian Basmati rice as potential tool for its geographical authenticity.

    Science.gov (United States)

    Lagad, Rupali A; Singh, Sunil K; Rai, Vinai K

    2017-02-15

    The increasing demand for premium priced Indian Basmati rice (Oryza sativa) in world commodity market causing fraudulent activities like adulteration, mislabelling. In order to develop authentication method for Indian Basmati rice, (87)Sr/(86)Sr ratios and REEs composition of Basmati rice, soil and water samples were determined and evaluated their ability as geographical tracer in the present study. In addition, the possible source of Sr in rice plant has also been examined. Basmati rice samples (n=82) showed (87)Sr/(86)Sr ratios in the range 0.71143-0.73448 and concentrations of 10 REEs (La, Ce, Pr, Nd, Sm, Eu, Gd, Dy, Er, Yb) in ppb levels. Statistical analysis showed strong correlation between (87)Sr/(86)Sr ratios of rice, silicate and carbonate fractions of soil. Good correlation and closeness of (87)Sr/(86)Sr of rice with water indicate its uptake in rice from water. Rice grown in southern Uttar Pradesh contains higher (87)Sr/(86)Sr compared to other region of Indo-Gangetic Plain due to higher (87)Sr/(86)Sr of the Ganga compared to other rivers. (87)Sr/(86)Sr ratios can be used as a tracer for differentiating Indian Basmati rice from the other country originated rice samples. PMID:27664633

  13. Rare earth elements and (87)Sr/(86)Sr isotopic characterization of Indian Basmati rice as potential tool for its geographical authenticity.

    Science.gov (United States)

    Lagad, Rupali A; Singh, Sunil K; Rai, Vinai K

    2017-02-15

    The increasing demand for premium priced Indian Basmati rice (Oryza sativa) in world commodity market causing fraudulent activities like adulteration, mislabelling. In order to develop authentication method for Indian Basmati rice, (87)Sr/(86)Sr ratios and REEs composition of Basmati rice, soil and water samples were determined and evaluated their ability as geographical tracer in the present study. In addition, the possible source of Sr in rice plant has also been examined. Basmati rice samples (n=82) showed (87)Sr/(86)Sr ratios in the range 0.71143-0.73448 and concentrations of 10 REEs (La, Ce, Pr, Nd, Sm, Eu, Gd, Dy, Er, Yb) in ppb levels. Statistical analysis showed strong correlation between (87)Sr/(86)Sr ratios of rice, silicate and carbonate fractions of soil. Good correlation and closeness of (87)Sr/(86)Sr of rice with water indicate its uptake in rice from water. Rice grown in southern Uttar Pradesh contains higher (87)Sr/(86)Sr compared to other region of Indo-Gangetic Plain due to higher (87)Sr/(86)Sr of the Ganga compared to other rivers. (87)Sr/(86)Sr ratios can be used as a tracer for differentiating Indian Basmati rice from the other country originated rice samples.

  14. Nd—Sr Isotope Geological Study on the Age of Armantai Ophiolite,Xinjiang,China

    Institute of Scientific and Technical Information of China (English)

    黄萱; 金成伟; 等

    1997-01-01

    Sm-Nd and Rb-Sr whole-rock isochron dating of the samples of cumulated gabbro,diabase and andesitic porphyrite from the Armantai ophiolite,Xinjiang,yielded the ages of 561±41(Ma(εNd(t)=6.1)and 392±17Ma(87Sr/86Sr)i=0.7041],which stand for the ages of creation and later metamorphism of the ophiolites,respectively,The creation environment of the Armantai ophiolites seems to a back-arc basin caused by the southward subduction of the the Armantai ophiloites seems to a back-arc basin caused by the southward subduction of the palaeo-Asia Ocean.

  15. Sm-Nd and Rb-Sr isotopic data on the sanukitoid intrusions of the Karelia, Baltic Shield

    Science.gov (United States)

    Kovalenko, A. V.; Savatenkov, V. M.

    2003-04-01

    Sanukitoid intrusions from the Baltic Shield form post-tectonic differentiated intrusions 2.74-2.72 Ga old (Chekulaev, 1999, Lobach-Zhuchenko et al., 2000). They are represented by alkaline and calc-alkaline types which have high mg# (up to 0.6), strong LREE enrichment (Ce(N)=80-150, Yb(N)=4-7, Ce(N)/Yb(N)>20), high Sr, Ba (>1000 ppm), P2O5 (up to 1.5%) and Cr, Ni concentrations. Some intrusions contain rocks varying from ultramafite to quartz syenite. All sanukitoids are intruded by lamprophyre dykes having similar geochemical signatures. In this study we focus on the Karelian greenstone terrain within the Baltic Shield, in which sanukitoids are restricted to the younger western and central domains (2.7-2.9 Ga). Sanukitoids appear to be absent from the older Vodlozero domain (>3.0 Ga) in eastern Karelia (Lobach-Zhuchenko et al., 2000, Lobach-Zhuchenko et al., in press). About 70 Sm-Nd isotopic data on the sanukitoids of the Karelia were obtained. There is the regional distinction of the isotope composition of the rocks between the Central and West Karelian domains. The initial Epsilon Nd values and TDM range from +1.1 to +2.0 and 2.70-2.85 Ga accordingly in the youngest Central Karelian domain. The West Karelian intrusions yield an initial Epsilon Nd of -0.3- +0.7 and give the older TDM of about 2.82-2.92 Ga. It is to be noted that some intrusions of the Central Karelia domain, occurred closely to the ancient Vodlozero domain, also exhibit a similar range of initial Epsilon Nd and TDM to the intrusions of the West Karelia. There are narrow Nd isotopic compositional ranges within the individual intrusions. Rb-Sr isotopic system was studied in sanukitoids and lamprophyres of differentiated Panozero intrusion, Central Karelia. The initial 87Sr/86Sr isotope ratios range from 0.7000 to 0.7021 in these rocks indicating the derivation of these magmas from depleted mantle. Very low initial 87Sr/86Sr isotope ratios of the sanukitoids confirm the Nd isotopic characteristics

  16. Accurate measurements of 129I concentration by isotope dilution using MC-ICPMS for half-life determination

    International Nuclear Information System (INIS)

    Determining the 129I concentration, a long-lived radionuclide present in spent nuclear fuel, is a major issue for nuclear waste disposal purpose. 129I also has to be measured in numerous environmental, nuclear and biological samples. To be able to accurately determine the 129I concentration, an analytical method based on the use of a multicollector-inductively coupled plasma mass spectrometer (MC-ICPMS) combined with an isotope dilution technique using an 127I spike, was developed. First, the influence of different media (HNO3, NaOH and TMAH) on natural 127I signal intensity and stability and on memory effects was studied. Then an analytical procedure was developed by taking into account the correction of blanks and interferences. Tellurium was chosen for instrumental mass bias correction, as no certified standards with suitable 127I/129I ratio are available. Finally, the results, reproducibility and uncertainties obtained for the 129I concentration determined by isotope dilution with a 127I spike are presented and discussed. The final expanded relative uncertainty obtained for the iodine-129 concentration was lower than 0.7% (k = 1). This precise 129I determination in association with further activity measurements of this nuclide on the same sample will render it possible to determine a new value of the 129I half-life with a reduced uncertainty (0.76%, k = 1).

  17. Accurate measurements of {sup 129}I concentration by isotope dilution using MC-ICPMS for half-life determination

    Energy Technology Data Exchange (ETDEWEB)

    Isnard, Helene; Nonell, Anthony; Marie, Mylene [Commissariat a l' Energie Atomique et aux Energies alternatives (CEA), Gif Sur Yvette (France). DEN, DPC, SEARS, LANIE; Chartier, Frederic [Commissariat a l' Energie Atomique et aux Energies alternatives (CEA), Gif Sur Yvette (France). DEN, DPC

    2016-05-01

    Determining the {sup 129}I concentration, a long-lived radionuclide present in spent nuclear fuel, is a major issue for nuclear waste disposal purpose. {sup 129}I also has to be measured in numerous environmental, nuclear and biological samples. To be able to accurately determine the {sup 129}I concentration, an analytical method based on the use of a multicollector-inductively coupled plasma mass spectrometer (MC-ICPMS) combined with an isotope dilution technique using an {sup 127}I spike, was developed. First, the influence of different media (HNO{sub 3}, NaOH and TMAH) on natural {sup 127}I signal intensity and stability and on memory effects was studied. Then an analytical procedure was developed by taking into account the correction of blanks and interferences. Tellurium was chosen for instrumental mass bias correction, as no certified standards with suitable {sup 127}I/{sup 129}I ratio are available. Finally, the results, reproducibility and uncertainties obtained for the {sup 129}I concentration determined by isotope dilution with a {sup 127}I spike are presented and discussed. The final expanded relative uncertainty obtained for the iodine-129 concentration was lower than 0.7% (k = 1). This precise {sup 129}I determination in association with further activity measurements of this nuclide on the same sample will render it possible to determine a new value of the {sup 129}I half-life with a reduced uncertainty (0.76%, k = 1).

  18. Isotopic Systematics (U, nitrate and Sr) of the F-Area Acidic Contamination Plume at the Savannah River Site: Clues to Contaminant History and Mobility

    Science.gov (United States)

    Christensen, J. N.; Conrad, M. E.; Bill, M.; Denham, M.; Wan, J.; Rakshit, S.; Stringfellow, W. T.; Spycher, N.

    2010-12-01

    Seepage basins in the F-Area of the Savannah River Site were used from 1955 to 1989 for the disposal of low-level radioactive acidic (ave. pH ˜2.9) waste solutions from site operations involving irradiated uranium billets and other materials used in the production of radionuclides. These disposal activities resulted in a persistent acidic groundwater plume (pH as low as 3.2) beneath the F-Area including contaminants such as tritium, nitrate, 90Sr, 129I and uranium and that has impinged on surface water (Four Mile Branch) about 600 m from the basins. After cessation of disposal in 1989, the basins were capped in 1991. Since that time, remediation has consisted of a pump-and-treat system that has recently been replaced with in situ treatment using a funnel-and-gate system with injection of alkaline solutions in the gates to neutralize pH. In order to delineate the history of contamination and the current mobility and fate of contaminants in F-Area groundwater, we have undertaken a study of variations in the isotopic compositions of U (234U/238U, 235U/238U, 236U/238U), Sr (87Sr/86Sr) and nitrate (δ15N, δ18O) within the contaminant plume. This data can be used to trace U transport within the plume, evaluate chemical changes of nitrate, and potentially track plume/sediment chemical interaction and trace the migration of 90Sr. We have analyzed a suite of groundwater samples from monitoring wells, as well as pore-water samples extracted from aquifer sediment cores to map out the isotopic variation within the plume. The isotopic compositions of U from well samples and porewater samples are all consistent with the variable burn-up of depleted U. The variation in U isotopic composition requires at least three different endmembers, without any significant influence of background natural U. The δ15N and δ18O of nitrate from F-Area plume groundwater are distinct both from natural and unaltered synthetic nitrate, and likely represents fractionation due to waste volume

  19. Accurate determination of selected pesticides in soya beans by liquid chromatography coupled to isotope dilution mass spectrometry.

    Science.gov (United States)

    Huertas Pérez, J F; Sejerøe-Olsen, B; Fernández Alba, A R; Schimmel, H; Dabrio, M

    2015-05-01

    A sensitive, accurate and simple liquid chromatography coupled with mass spectrometry method for the determination of 10 selected pesticides in soya beans has been developed and validated. The method is intended for use during the characterization of selected pesticides in a reference material. In this process, high accuracy and appropriate uncertainty levels associated to the analytical measurements are of utmost importance. The analytical procedure is based on sample extraction by the use of a modified QuEChERS (quick, easy, cheap, effective, rugged, safe) extraction and subsequent clean-up of the extract with C18, PSA and Florisil. Analytes were separated on a C18 column using gradient elution with water-methanol/2.5 mM ammonium acetate mobile phase, and finally identified and quantified by triple quadrupole mass spectrometry in the multiple reaction monitoring mode (MRM). Reliable and accurate quantification of the analytes was achieved by means of stable isotope-labelled analogues employed as internal standards (IS) and calibration with pure substance solutions containing both, the isotopically labelled and native compounds. Exceptions were made for thiodicarb and malaoxon where the isotopically labelled congeners were not commercially available at the time of analysis. For the quantification of those compounds methomyl-(13)C2(15)N and malathion-D10 were used respectively. The method was validated according to the general principles covered by DG SANCO guidelines. However, validation criteria were set more stringently. Mean recoveries were in the range of 86-103% with RSDs lower than 8.1%. Repeatability and intermediate precision were in the range of 3.9-7.6% and 1.9-8.7% respectively. LODs were theoretically estimated and experimentally confirmed to be in the range 0.001-0.005 mg kg(-1) in the matrix, while LOQs established as the lowest spiking mass fractionation level were in the range 0.01-0.05 mg kg(-1). The method reliably identifies and quantifies the

  20. Geochemical and Isotopic (Sr, U) Tracing of Weathering Processes Controlling the Recent Geochemical Evolution of Soil Solutions in the Strengbach Catchment (Vosges, France)

    Science.gov (United States)

    Chabaux, F. J.; Prunier, J.; Pierret, M.; Stille, P.

    2012-12-01

    The characterization of the present-day weathering processes controlling the chemical composition of waters and soils in natural ecosystems is an important issue to predict and to model the response of ecosystems to recent environmental changes. It is proposed here to highlight the interest of a multi-tracer geochemical approach combining measurement of major and trace element concentrations along with U and Sr isotopic ratios to progress in this topic. This approach has been applied to the small granitic Strengbah Catchment, located in the Vosges Mountain (France), used and equipped as a hydro-geochemical observatory since 1986 (Observatoire Hydro-Géochimique de l'Environnement; http://ohge.u-strasbg.fr). This study includes the analysis of major and trace element concentrations and (U-Sr) isotope ratios in soil solutions collected within two soil profiles located on two experimental plots of this watershed, as well as the analysis of soil samples and vegetation samples from these two plots The depth variation of elemental concentration of soil solutions confirms the important influence of the vegetation cycling on the budget of Ca, K, Rb and Sr, whereas Mg and Si budget in soil solutions are quasi exclusively controlled by weathering processes. Variation of Sr, and U isotopic ratios with depth also demonstrates that the sources and biogeochemical processes controlling the Sr budget of soil solutions is different in the uppermost soil horizons and in the deeper ones, and clearly influence by the vegetation cycling.

  1. Comprehensive analysis for major, minor and trace element contents and Sr-Nd-Pb-Hf isotope ratios in sediment reference materials, JSd-1 and MAG-1

    Digital Repository Service at National Institute of Oceanography (India)

    Nath, B.N.; Makishima, A.; Noordmann, J.; Tanaka, R.; Nakamura, E.

    In view of the requirement of a well-characterized and easily available aquatic sediment reference material, a comprehensive analysis comprising of fifty major, minor and trace elements as well as Sr–Nd–Pb–Hf isotopes were carried out...

  2. Rb-Sr, Sm-Nd, K-Ca, O, and H isotopic study of Cretaceous-Tertiary boundary sediments, Caravaca, Spain Evidence for an oceanic impact site

    Energy Technology Data Exchange (ETDEWEB)

    Depaolo, D.J.; Kyte, F.T.; Marshall, B.D.

    1983-09-01

    The results of isotopic and trace-element-abundance analyses of Ir-enriched Cretaceous-Tertiary-boundary clay sediments from Caravaca, Spain, and of adjacent carbonate and marl layers, are presented. Acetic-acid and HCl leachates and residues were analyzed by isotope dilution to determine K, Rb, Sr, Sm, and Nd concentrations and Sr-87/Sr-86 and Nd-143/Nd-144 ratios. The stable isotope ratios delta-D, delta-(C-13), and delta-(0-18) were also determined. The results are presented in tables and graphs and compared with published data on the Caravaca sediments and on samples from other locations. The boundary clay is found to be distinguished from the adjacent layers by its isotopic ratios and to be of mainly terrestrial, lithospheric (deeper than 3-km) origin. Although submarine-weathering effects are evident and difficult to quantify, the degree of variation in Ni, Ir, Sr, and REE concentrations is considered too large to be attributed to postdepositional processes alone. These findings are seen as evidence for the ocean impact of a large single asteroid producing a worldwide blanket of ejecta, a large injection of water vapor into the atmosphere, and perhaps a gigantic tsunami, at the end of the Cretaceous period.

  3. Cluster emission in superdeformed Sr isotopes in the ground state and formed in heavy-ion reaction

    Indian Academy of Sciences (India)

    K P Santhosh; Antony Joseph

    2005-01-01

    Cluster decay of superdeformed 76,78,80Sr isotopes in their ground state are studied taking the Coulomb and proximity potential as the interacting barrier for the post-scission region. The predicted 1/2 values are found to be in close agreement with those values reported by the preformed cluster model (PCM). Our calculation shows that these nuclei are stable against both light and heavy cluster emissions. We studied the decay of these nuclei produced as an excited compound system in heavy-ion reaction. It is found that inclusion of excitation energy increases the decay rate (decreases 1/2 value) considerably and these nuclei become unstable against decay. These findings support earlier observation of Gupta et al based on PCM.

  4. Sr-Nd isotope changes of late cretaceous to early miocene volcanic rocks in central Chile (33oS)

    International Nuclear Information System (INIS)

    A longitudinal depression, the Central Valley, separates the Coast Range from the Andean Cordillera in central Chile. It contains volcanic and volcaniclastic rocks of Late Cretaceous to Tertiary age deposited in a continental environment, and partly eroded Tertiary volcanic complexes. The age of the rocks at the northern end of the Central Valley and their grouping in formations have been a long-standing controversy in Chilean geology (Thomas, 1958; Aguirre, 1960; Drake et al., 1976; Vergara and Drake, 1979; Thiele, 1980; Moscoso et al., 1982; Gana and Wall, 1997; Lopez-Escobar and Vergara, 1997; Selles, 1999). Here, we report new 40Ar/39Ar data and Sr-Nd isotope ratios for lavas, pyroclastic flows and associated subvolcanic rocks from this part of central Chile (au)

  5. Rb-Sr, Sm-Nd, K-Ca, O, and H isotopic study of Cretaceous-Tertiary boundary sediments, Caravaca, Spain: Evidence for an oceanic impact site

    Energy Technology Data Exchange (ETDEWEB)

    DePaolo, D.J.; Kyte, F.T.; Marshall, B.D.; O' Neil, J.R.; Smit, J.

    1983-09-01

    Isotopic ratios and trace element abundances were measured on samples of IR-enriched clay at the Cretaceous-Tertiary boundary, and in carbonate and marl from 5 cm below and 3 cm above the boundary. Samples were leached with acetic acid to remove carbonate, and with hydrochloric acid. Leachates and residues were measured. The Sr, Nd, O and H isotopic compositions of the boundary clay residues are distinct from those of the stratigraphically neighboring materials. The data indicate that most of the clay material was derived from a terrestrial source with relatively low /sup 87/Sr//sup 86/Sr and high /sup 143/Nd//sup 144/Nd ratios. The delta/sup 18/O data suggest that the detritus has been modified by submarine weathering. K-Ca and Rb-Sr systematics, as well as O isotope ratios of K-feldspar spherules within the boundary clay, suggest that they are predominantly authigenic and may have formed after the time of deposition. However, Sm-Nd and Rb-Sr isotopic data indicate that the spherules contain relict material that provides information on the nature of the original detritus. The isotopic evidence for foreign terrestrial detritus in the boundary clay, the low rare earth element concentrations and high Ni concentration, support the hypothesis of a terminal Cretaceous asteroidal impact that produced a global layer of fallout. The data are most easily explained if the impact sites was on oceanic crust rather than continental crust, and if a substantial fraction of the fallout was derived from relatively deep within the lithosphere (> 3 km). This would probably require a single large impactor. 60 references.

  6. Age and petrology of the Kalaupapa Basalt, Molokai, Hawaii ( geochemistry, Sr isotopes).

    Science.gov (United States)

    Clague, D.A.

    1982-01-01

    The post-erosional Kalaupapa Basalt on East Molokai, Hawaii, erupted between 0.34 and 0.57 million years ago to form the Kalaupapa Peninsula. The Kalaupapa Basalt ranges in composition from basanite to lava transitional between alkalic and tholeiitic basalt. Rare-earth and other trace-element abundances suggest that the Kalaupapa Basalt could be generated by 11-17% partial melting of a light-REE-enriched source like that from which the post-erosional lavas of the Honolulu Group on Oahu were generated by 2-11% melting. The 87Sr/86Sr ratios of the lavas range from 0.70320 to 0.70332, suggesting that the variation in composition mainly reflects variation in the melting process rather than heterogeneity of sources. The length of the period of volcanic quiescence that preceded eruption of post-erosional lavas in the Hawaiian Islands decreased as volcanism progressed from Kauai toward Kilauea. - Authors

  7. Toward complete isotopic analysis of individual presolar silicon carbide grains : C, N, Si, Sr, Zr, Mo, and Ba in single grains of type X.

    Energy Technology Data Exchange (ETDEWEB)

    Pellin, M. J.; Calaway, W. F.; Davis, A. M.; Lewis, R. S.; Amari, S.; Clayton, R. N.

    2000-03-01

    Presolar silicon carbide grains form in a variety of types of stars, including asymptotic giant branch red giant stars and supernovae. The dominant mechanisms of heavy element nucleosynthesis, the s-process and r-process, are thought to occur mainly in AGB stars and supernovae, respectively [1]. We have previously reported that mainstream SiC grains have strong enrichments in the s-process isotopes of Sr, Zr and Mo [2-4] and initial results for X-type SiC grains showing enrichments in the r-process isotopes of Mo[5]. We report here the first measurements of Zr, Sr, and Ba isotopes along with expanded studies of Mo in individual X-type SiC grains, which have previously been identified as having formed from supernova ejects.

  8. U and Sr Isotopes in ground water and calcite, Yucca Mountain, Nevada: Evidence against upwelling water

    Science.gov (United States)

    Stuckless, J.S.; Peterman, Z.E.; Muhs, D.R.

    1991-01-01

    Hydrogenic calcite and opaline silica deposits in fault zones at Yucca Mountain, Nevada, have created considerable public and scientific controversy because of the possible development of a high-level nuclear waste repository at this location. Strontium and uranium isotopic compositions of hydrogenic materials were used to test whether the veins could have formed by upwelling of deep-seated waters. The vein deposits are isotopically distinct from ground water in the two aquifers that underlie Yucca Mountain, indicating that the calcite could not have precipitated from ground water. The data are consistent with a surficial origin for the hydrogenic deposits.

  9. Rb-Sr and Sm-Nd isotopic study of the Glen Mountains layered complex: Initiation of rifting within the southern Oklahoma aulacogen

    Science.gov (United States)

    Lambert, David D.; Unruh, D. M.; Gilbert, M. Charles

    1988-01-01

    Rb-Sr and Sm-Nd isotopic data for rocks and minerals of the Glen Mountains layered complex (GMLC), a midcontinent mafic layered intrusion in the Wichita Mountains of southwestern Oklahoma, constrain the time of initiation of rifting within the southern Oklahoma aulacogen and provide information on the chemistry of the early Paleozoic mantle. Four whole-rock samples define a Rb-Sr isochron corresponding to a maximum crystallization age of 577 ±165 Ma and an initial Sr isotopic composition of 0.70359 ±2. These whole-rock analyses do not define a Sm-Nd isochron; rather, they display a significant range in initial Nd isotopic composition (ɛNd = 3.63-5.35). A three-point Sm-Nd mineral-whole-rock (internal) isochron for an anorthositic gabbro provides a crystallization age of 528 ±29 Ma. These data suggest that the GMLC was emplaced into the southern Oklahoma aulacogen during the initial phase of rifting along the southern margin of the North American craton in the early Paleozoic. This Sm-Nd internal isochron age is within analytical uncertainty of U-Pb zircon ages for granites and rhyolites from the Wichita Mountains; therefore, mafic and felsic magmatism may have been contemporaneous within the rift during the early stages of development. Hybrid rocks and composite dikes in the Wichita Mountains provide field evidence for contemporaneous mafic and felsic magmas. Initial Sr and Nd isotopic data suggest that magmas parental to the GMLC were derived from a depleted mantle source. However, Nd isotopic data for the GMLC plot distinctly below data for the depleted mantle source cited by DePaolo and thus suggest that the parental magmas of the GMLC were either contaminated by Proterozoic crust of the southern midcontinent or were derived from a heterogeneous mantle source region that had variable initial Nd isotopic compositions.

  10. Geochemistry of Late Mesozoic mafic dykes in western Fujian Province of China:Sr-Nd isotope and trace element constraints

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The Bancun diabase dyke and the Bali hornblende gabbro dyke in western Fuiian Province were emplaced in the Early and Late Cretaceous periods,respectively;the former is designated to calc-alkaline series and the latter to K-high-calc-alkaline rock series.Both the dykes are characterized by such geochemical characteristics as high Al and Na2O>K2O.As for the Bancun dyke,A12O3=16.32%-17.54%and K2O/Na2O=0.65-0.77;as for the Bali dyke,A12O3=16.89%-17.81%and K2O,Na2O=O.93-O.99.Both the Bancun and Bali mafic dykes are relatively endched in LILE and LREE,but depleted in HSFE, displaying the geochemical characteristics of continental marginal arc,with high initial Sr isotopic ratios and low εNd values,The (87Sr/86Sr)i ratios of the Bancun diabase dyke are within the range of 0.708556-0.70903 and their εNd(t)values vary between-6.8 and-6.3;those of the Bali hornblende dyke are within the range of 0.708556-0.710746 and their εNd(t) values are -4.7--4.7,showing the characteristics of enriched mantle EM Ⅱ.The isotope and trace element data showed that the mafic dykes have not experienced obvious crustal contamination,and metasomatism caused by subduction fluids is the main factor leading to LILE and UREE enrichments.The enriched mantle is the source region for the mafic dykes,and mixing of subduction fluid metasomatized enriched mantle and EM Ⅱ-type mantle constituted the mantle source region of both the Bancun and Bali mafic dykes.Upwelling of the asthenosphere mantle provided sufficient heat energy for the generation of magmas.In accordance with the discrimination diagram of their tectonic settings as well as their trace element geochemical characteristics,it is considered that the dykes both at Bancun and Bali possess the characteristics of continental marginal arc,revealing the tectonic environment of formation of the mafic dykes,the continental dynamic background as an intraplate tensional belt in which the mafic dykes were emplaced.Meanwhile,it is also indicated

  11. Petrology, Geochemistry and Nd-Sr-Pb Isotopic Properties of Volcanic Rocks in Daheishan Island, Penglai, Shandong Province

    Institute of Scientific and Technical Information of China (English)

    Fu Yongtao; Li Anchun

    2003-01-01

    The major elements, trace elements, K-Ar age and Sr-Nd-Pb isotopic systems of the Cenozoic volcanic rocks in Daheishan Island and Cishan, Penglai, Shandong Province are measured. The volcanic rocks ( olivine-nephelinite and nepheline-basanite ) in Daheishan Island erupted periodically in an interval of 0.32 Ma, from 8.72 Ma, 8.39 Ma, 8.08 Ma to 7.73 Ma. The volcanic rocks are all rich in light REEs. They are similar to the OIB-type alkali basalt in the trace elements normalized model by primordial mantle: rich in high field elements such as Nb and Ta, and imcompatible elements such as Cs, Rb, Ba, Th, U. The volcanic rocks show a depletion of K and Rb elements. It is suggested by the trace elements that the olivine-nephelinite in Daheishan Island is originated from deep resources under the continental mantle. ε Nd (0) values of the volcanic rocks in Daheishan Island and Cisban are 5.31 ~ 8.51 and 7.33 respectively, suggesting that the volcanic rocks are from the depleted mantle resources, which have higher Sm/Nd ratios than the CHUR. 143Nd /144Nd ratios of Daheishan Island olivine-nephelinite and Cishan alkali basalts are 0.512 910 ~ 0.513 074 and 0.513 014 respectively. The 87Sr /86Sr of Daheishan Island volcanic rocks are lower than that of Cishan, 0.703 427 ~ 0.703 482 and 0.703 895 respectively. The Daheishan Island olivinenephelinite has the Pb isotopic values as follows: 206Pb /204pb = 18.028 9 ~ 17.972 8, 207Pb /204pb= 15.435 8 ~ 15.402 2 and 208Pb /204Pb = 38.087 6 ~ 37.997 5, lower than those of Cishan basanite. The Cishan basanite has 206Pb /204pb = 18.240 1, 207Pb /204Pb = 15.564 5 and 208Pb /204pb = 38.535. The authors suggest that the olivine-nephelinite in Daheishan Island is similar to the E-type MORB or Hawaii OIB, and the alkali basalts in Cishan similar to the Kerguelen OIB. The dominant mantle components of DM+PREMA and perhaps DM ( Dupal type ) are the dominant mantle components for volcanic rocks in Daheishan Island and Cishan. The

  12. Geochemical and Sr-Nd-Pb isotopic evidence for ancient lower continental crust beneath the Xi Ujimqin area of NE China

    Science.gov (United States)

    Gao, Xiaofeng; Guo, Feng; Xiao, Peixi; Kang, Lei; Xi, Rengang

    2016-05-01

    The Central Asian Orogenic Belt (CAOB) is the largest Phanerozoic accretionary orogen on Earth. The role that Precambrian continental microblocks played in its formation, however, remains a highly controversial topic. New zircon U-Pb age data and whole-rock geochemical and Sr-Nd-Pb isotopic studies on Permian (253-251 Ma) andesites from the Xi Ujimqin area provide the first evidence for the existence of a continental lower mafic crust in the eastern segment of the CAOB. These Permian lavas generally have chemical compositions similar to experimental melts of garnet pyroxenites. Based on Sr-Nd-Pb isotopic compositional differences, they can be further subdivided into two groups. Group 1 has moderately radiogenic Sr (87Sr/86Sr(i) = 0.7060-0.7062) and nonradiogenic Nd (εNd(t) = - 9.0-8.3) and Pb (e.g., 206Pb/204Pb = 17.18-17.23) isotopic compositions similar to the ancient lower mafic crust beneath the North China Craton (NCC). Compared with Group 1, Group 2 has less radiogenic Sr (87Sr/86Sr(i) = 0.7051-0.7055), and more radiogenic Nd (εNd(t) = - 0.2-+1.4) and Pb (e.g., 206Pb/204Pb = 18.04-18.20) isotopic compositions as observed in the Phanerozoic granitoids and felsic lavas of the CAOB. The combined geochemical and isotopic data indicate that Group 1 was derived from ancient lower mafic crust of the NCC affinity, with a residual assemblage of pyroxene + plagioclase + amphibole. The source for Group 2 was a mixture of ancient lower mafic crust and a juvenile crustal component, and melting left a residue of orthopyroxene + clinopyroxene + plagioclase + garnet + amphibole. Generation of these two types of late Permian andesites favors a model whereby breakoff of a subducted slab and subsequent lithospheric extension triggered extensive asthenospheric upwelling and melting of the continental mafic lower crust of the eastern CAOB. The discovery of ancient lower continental crust of the NCC affinity in the CAOB implies that the NCC experienced continental breakup during

  13. Multiple linear regression for isotopic measurements

    Science.gov (United States)

    Garcia Alonso, J. I.

    2012-04-01

    There are two typical applications of isotopic measurements: the detection of natural variations in isotopic systems and the detection man-made variations using enriched isotopes as indicators. For both type of measurements accurate and precise isotope ratio measurements are required. For the so-called non-traditional stable isotopes, multicollector ICP-MS instruments are usually applied. In many cases, chemical separation procedures are required before accurate isotope measurements can be performed. The off-line separation of Rb and Sr or Nd and Sm is the classical procedure employed to eliminate isobaric interferences before multicollector ICP-MS measurement of Sr and Nd isotope ratios. Also, this procedure allows matrix separation for precise and accurate Sr and Nd isotope ratios to be obtained. In our laboratory we have evaluated the separation of Rb-Sr and Nd-Sm isobars by liquid chromatography and on-line multicollector ICP-MS detection. The combination of this chromatographic procedure with multiple linear regression of the raw chromatographic data resulted in Sr and Nd isotope ratios with precisions and accuracies typical of off-line sample preparation procedures. On the other hand, methods for the labelling of individual organisms (such as a given plant, fish or animal) are required for population studies. We have developed a dual isotope labelling procedure which can be unique for a given individual, can be inherited in living organisms and it is stable. The detection of the isotopic signature is based also on multiple linear regression. The labelling of fish and its detection in otoliths by Laser Ablation ICP-MS will be discussed using trout and salmon as examples. As a conclusion, isotope measurement procedures based on multiple linear regression can be a viable alternative in multicollector ICP-MS measurements.

  14. Chemical and U-Sr isotopic variations of stream and source waters at a small catchment scale (the Strengbach case; Vosges mountains; France)

    Science.gov (United States)

    Pierret, M. C.; Stille, P.; Prunier, J.; Viville, D.; Chabaux, F.

    2014-03-01

    This is the first comprehensive study dealing with major and trace element data as well as 87Sr/86Sr isotope and (234U/238U) activity ratios (AR) determined on the totality of springs and brooks of the Strengbach catchment. It shows that the small and more or less monolithic catchment drains different sources and streamlets with very different isotopic and geochemical signatures. Different parameters control the diversity of the source characteristics. Of importance is especially the hydrothermal overprint of the granitic bedrock, which was stronger for the granite from the northern than from the southern slope; also significant are the different meteoric alteration processes of the bedrock causing the formation of 0.5 to 9 m thick saprolite and above the formation of an up to 1 m thick soil system. These processes mainly account for springs and brooks from the northern slope having higher Ca/Na, Mg/Na, Sr/Na ratios but lower 87Sr/86Sr isotopic ratios than those from the southern slope. The chemical compositions of the source waters in the Strengbach catchment are only to a small extent the result of alteration of primary bedrock minerals and rather reflect dissolution/precipitation processes of secondary mineral phases like clay minerals. The (234U/238U) AR, however, are decoupled from the 87Sr/86Sr isotope system and reflect to some extent the level of altitude of the source and, thus, the degree of alteration of the bedrock. The sources emerging at high altitudes have circulated through already weathered materials (saprolite and fractured rock depleted in 234U) implying (234U/238U) AR < 1, which is uncommon for surface waters. Preferential flow paths along constant fractures in the bedrocks might explain the over time homogeneous U AR of the different spring waters. However, the geochemical and isotopic variations of stream waters at the outlet of the catchment are controlled by variable contributions of different springs depending on the hydrological conditions

  15. A hydrogen gas-water equilibration method produces accurate and precise stable hydrogen isotope ratio measurements in nutrition studies

    Science.gov (United States)

    Stable hydrogen isotope methodology is used in nutrition studies to measure growth, breast milk intake, and energy requirement. Isotope ratio MS is the best instrumentation to measure the stable hydrogen isotope ratios in physiological fluids. Conventional methods to convert physiological fluids to ...

  16. Tracing Anthropogenic Salinity Inputs to the Semi-arid Rio Grande River: A Multi-isotope Tracer (U, S, B and Sr) Approach

    Science.gov (United States)

    Garcia, S.; Nyachoti, S. K.; Ma, L.; Szynkiewicz, A.; McIntosh, J. C.

    2015-12-01

    High salinity in the Rio Grande has led to severe reductions in crop productivity and accumulation of salts in soils. These pressing issues exist for other arid rivers worldwide. Salinity contributions to the Rio Grande have not been adequately quantified, especially from agriculture, urban activities, and geological sources. Here, we use major element concentrations and U, S, B, Sr isotopic signatures to fingerprint the salinity sources. Our study area focuses on a 200 km long stretch of the Rio Grande from Elephant Butte Reservoir, NM to El Paso, TX. River samples were collected monthly from 2014 to 2015. Irrigation drains, groundwater wells, city drains and wastewater effluents were sampled as possible anthropogenic salinity end-members. Major element chemistry, U, S and Sr isotope ratios in the Rio Grande waters suggest multiple salinity inputs from geological, agricultural, and urban sources. Natural upwelling of groundwater is significant for the Rio Grande near Elephant Butte, as suggested by high TDS values and high (234U/238U), 87Sr/86Sr, δ34S ratios. Agricultural activities (e.g. flood irrigation, groundwater pumping, fertilizer use) are extensive in the Mesilla Valley. Rio Grande waters from this region have characteristic lower (234U/238U), 87Sr/86Sr, and δ34S ratios, with possible agricultural sources from use of fertilizers and gypsum. Agricultural practices during flood irrigation also intensify evaporation of Rio Grande surface water and considerably increase water salinity. Shallow groundwater signatures were also identified at several river locations, possibly due to the artificial pumping of local groundwater for irrigation. Impacts of urban activities to river chemistry (high NO3 and B concentrations) were evident for locations downstream to Las Cruces and El Paso wastewater treatment plants, supporting the use of the B isotope as an urban salinity tracer. This study improves our understanding of human impacts on water quality and elemental

  17. Direct High-Precision Measurements of the (87)Sr/(86)Sr Isotope Ratio in Natural Water without Chemical Separation Using Thermal Ionization Mass Spectrometry Equipped with 10(12) Ω Resistors.

    Science.gov (United States)

    Li, Chao-Feng; Guo, Jing-Hui; Chu, Zhu-Yin; Feng, Lian-Jun; Wang, Xuan-Ce

    2015-07-21

    Thermal ionization mass spectrometry (TIMS) allows excellent precision for determining Sr isotope ratios in natural water samples. Traditionally, a chemical separation procedure using cation exchange resin has been employed to obtain a high purity Sr fraction from natural water, which makes sample preparation time-consuming. In this study, we present a rapid and precise method for the direct determination of the Sr isotope ratio of natural water using TIMS equipped with amplifiers with two 10(12) Ω resistors. To eliminate the (87)Rb isobaric interference, Re ribbons are used as filaments, providing a significant advantage over W ribbons in the inhibition of Rb(+) emission, based on systematically examining a series of NIST SRM987 standard doping with various amounts of Rb using Re and W ribbons. To validate the applicability of our method, twenty-two natural water samples, including different water types (rain, snow, river, lake and drinking water), that show a large range in Sr content variations (2.54-922.8 ppb), were collected and analyzed from North and South China. Analytical results show good precision (0.003-0.005%, 2 RSE) and the method was further validated by comparative analysis of the same water with and without chemical separation. The method is simple and rapid, eliminates sample preparation time, and prevents potential contamination during complicated sample-preparation procedures. Therefore, a high sample throughput inherent to the TIMS can be fully utilized.

  18. Saturation of Deformation and Identical Bands in Very-Neutron Rich Sr Isotopes

    CERN Multimedia

    2002-01-01

    The present proposal aims at establishing nuclear properties in an isotopic chain showing unique features. These features include the saturation of ground state deformation at its onset and the existence of ground state identical bands in neighbouring nuclei with the same deformation. The measurements should help to elucidate the role played by the proton-neutron residual interaction between orbitals with large spatial overlap, i.e. $\\pi g _{9/2} \

  19. Chemical and U-Sr isotopic variations of stream and source waters at a small catchment scale (the Strengbach case; Vosges mountains; France

    Directory of Open Access Journals (Sweden)

    M. C. Pierret

    2014-03-01

    Full Text Available This is the first comprehensive study dealing with major and trace element data as well as 87Sr/86Sr isotope and (234U/238U activity ratios (AR determined on the totality of springs and brooks of the Strengbach catchment. It shows that the small and more or less monolithic catchment drains different sources and streamlets with very different isotopic and geochemical signatures. Different parameters control the diversity of the source characteristics. Of importance is especially the hydrothermal overprint of the granitic bedrock, which was stronger for the granite from the northern than from the southern slope; also significant are the different meteoric alteration processes of the bedrock causing the formation of 0.5 to 9 m thick saprolite and above the formation of an up to 1 m thick soil system. These processes mainly account for springs and brooks from the northern slope having higher Ca/Na, Mg/Na, Sr/Na ratios but lower 87Sr/86Sr isotopic ratios than those from the southern slope. The chemical compositions of the source waters in the Strengbach catchment are only to a small extent the result of alteration of primary bedrock minerals and rather reflect dissolution/precipitation processes of secondary mineral phases like clay minerals. The (234U/238U AR, however, are decoupled from the 87Sr/86Sr isotope system and reflect to some extent the level of altitude of the source and, thus, the degree of alteration of the bedrock. The sources emerging at high altitudes have circulated through already weathered materials (saprolite and fractured rock depleted in 234U implying (234U/238U AR It appears that the (234U/238U AR is an appropriate very important tracer for studying and deciphering the contribution of the different source fluxes at the catchment scale because this unique geochemical parameter is different for each individual spring and at the same time remains unchanged for each of the springs with changing discharge and fluctuating

  20. Rb-Sr and Sm-Nd isotopic study of the Glen Mountains layered complex: initiation of rifting within the southern Oklahoma aulacogen

    Energy Technology Data Exchange (ETDEWEB)

    Lambert, D.D.; Unruh, D.M.; Gilbert, M.C.

    1988-01-01

    Rb-Sr and Sm-Nd isotopic data for rocks and minerals of the Glen Mountains layered complex (GMLC), a midcontinent mafic layered intrusion in the Wichita Mountains of southwestern Oklahoma, constrain the time of initiation of rifting within the southern Oklahoma aulacogen and provide information on the chemistry of the early Paleozoic mantle. Four whole-rock samples define a Rb-Sr isochron corresponding to a maximum crystallization age of 577 +/- 165 Ma and an initial Sr isotopic composition of 0.70359 +/- 2. A three-point Sm-Nd mineral-whole-rock (internal) isochron for an anorthositic gabbro provides a crystallization age of 528 +/- 29 Ma. These data suggest that the GMLC was emplaced into the southern Oklahoma aulacogen during the initial phase of rifting along the southern margin of the North American craton in the early Paleozoic. This Sm-Nd internal isochron age is within analytical uncertainty of U-Pb zircon ages for granites and rhyolites from the Wichita Mountains; therefore, mafic and felsic magmatism may have been contemporaneous within the rift during the early stages of development. Hybrid rocks and composite dikes in the Wichita Mountains provide field evidence for contemporaneous mafic and felsic magmas. Initial Sr and Nd isotopic data suggest that magmas parental to the GMLC were derived from a depleted mantle source. However, Nd isotopic data for the GMLC plot distinctly below data for the depleted mantle source cited by DePaolo and thus suggest that the parental magmas of the GMLC were either contaminated by Proterozoic crust of the southern midcontinent or were derived from a heterogenous mantle source region that had variable initial Nd isotopic compositions.

  1. Zircon U-Pb geochronology, Sr-Nd-Hf isotopic composition and geological significance of the Late Triassic Baijiazhuang and Lvjing granitic plutons in West Qinling Orogen

    Science.gov (United States)

    Duan, Meng; Niu, Yaoling; Kong, Juanjuan; Sun, Pu; Hu, Yan; Zhang, Yu; Chen, Shuo; Li, Jiyong

    2016-09-01

    The Qinling Orogen was a consequence of continental collision of the South China Craton with the North China Craton in the Triassic and caused widespread granitoid magmatism. However, the petrogenesis of these granitoids remains controversial. In this paper, we choose the Baijiazhuang (BJZ) and Lvjing (LJ) plutons in the West Qinling Orogen for a combined study of the zircon U-Pb geochronology, whole-rock major and trace element compositions and Sr-Nd-Hf isotopic characteristics. We obtained zircon crystallization ages of ~ 216 Ma and ~ 212 Ma for the BJZ and the LJ plutons, respectively. The granitoid samples from both plutons have high K2O metaluminous to peraluminous compositions. They are enriched in large ion lithophile elements (LILEs), light rare earth elements (LREEs) and depleted in high field-strength elements (HFSEs) with significant negative Eu anomalies. The BJZ samples have initial Sr isotopic ratios of 0.7032 to 0.7078, εNd(t) of - 10.99 to - 8.54 and εHf (t) of - 10.22 to - 6.41. The LJ granitoids have initial Sr isotopic ratios of 0.7070 to 0.7080, εNd(t) of - 5.37 to - 4.58 and εHf(t) of - 3.64 to - 1.78. The enriched isotopic characteristics of the two plutons are consistent with their source being dominated by ancient continental crust. However, two BJZ samples show depleted Sr isotope compositions, which may infer possible involvement of mantle materials. Mantle-derived melt, which formed from partial melting of mantle wedge peridotite facilitated by dehydration of the subducted/subducting Mianlue ocean crust, provide the required heat for the crustal melting while also contributing to the compositions of these granitoids. That is, the two granitic plutons are magmatic responses to the closure of the Mianlue ocean basin and the continental collision between the Yangtze and South Qinling crustal terranes.

  2. Origin of the Red Dog Zn-Pb-Ag deposits, Brooks Range, Alaska: Evidence from regional Pb and Sr isotope sources

    Science.gov (United States)

    Ayuso, R.A.; Kelley, K.D.; Leach, D.L.; Young, L.E.; Slack, J.F.; Wandless, G.; Lyon, A.M.; Dillingham, J.L.

    2004-01-01

    Pb and Sr isotope data were obtained on the shale-hosted Zn-Pb-Ag Red Dog deposits (Qanaiyaq, Main, Aqqaluk, and Paalaaq), other shale-hosted deposits near Red Dog, and Zn-Pb-Ag sulfide and barite deposits in the western and central Brooks Range. The Red Dog deposits and other shale-hosted Zn-Pb-Ag deposits near Red Dog are hosted in the Mississippian Kuna Formation, which is underlain by a sequence of marine-deltaic clastic rocks of the Upper Devonian to Lower Mississippian Endicott Group. Ag-Pb-Zn vein-breccias are found in the Endicott Group. Galena formed during the main mineralization stages in the Red Dog deposits and from the Anarraaq and Wulik deposits have overlapping Pb isotope compositions in the range 206Pb/204Pb = 18.364 to 18.428, 207Pb/204Pb = 15.553 to 15.621, and 208Pb/204Pb = 38.083 to 38.323. Galena and sphalerite formed during the main ore-forming stages in the Red Dog deposits define a narrow field on standard uranogenic and thorogenic Pb isotope diagrams. Lead in sulfides of the Red Dog district is less radiogenic (238U/204Pb: ?? = 9.51-9.77) than is indicated by the average crustal lead evolution model (?? = 9.74), a difference consistent with a long history of evolution at low ratios of ?? before the Carboniferous. The homogeneous regional isotopic reservoir of Pb may indicate large-scale transport and leaching of minerals with various ?? ratios and Th/Pb ratios. Younger and genetically unrelated fluids did not significantly disturb the isotopic compositions of galena and sphalerite after the main mineralization event in the Red Dog district. Some pyrite shows evidence of minor Pb remobilization. The overall lead isotope homogeneity in the shale-hosted massive sulfide deposits is consistent with three types of control: a homogeneous regional source, mixing of lead during leaching of a thick sedimentary section and fluid transport, or mixing at the site of deposition. Isotopic variability of the hydrothermal fluids, as represented by galena

  3. Sr, Nd, and Pb isotopes of ultramafic xenoliths in volcanic rocks of Eastern China: enriched components EMI and EMII in subcontinental lithosphere

    Science.gov (United States)

    Tatsumoto, M.; Basu, A.R.; Wankang, H.; Junwen, W.; Guanghong, X.

    1992-01-01

    The UThPb, SmNd, and RbSr isotopic systematics of mafic and ultramafic xenolithic rocks and associated megacrystic inclusions of aluminous augite and garnet, that occur in three alkalic volcanic suites: Kuandian in eastern Liaoning Province, Hanluoba in Hebei Province, and Minxi in western Fujian Province, China are described. In various isotopic data plots, the inclusion data invariably fall outside the isotopic ranges displayed by the host volcanic rocks, testifying to the true xenolithic nature of the inclusions. The major element partitioning data on Ca, Mg, Fe, and Al among the coexisting silicate minerals of the xenoliths establish their growth at ambient mantle temperatures of 1000-1100??C and possible depths of 70-80 km in the subcontinental lithosphere. Although the partitioning of these elements reflects equilibrium between coexisting minerals, equilibria of the Pb, Nd, and Sr isotopic systems among the minerals were not preserved. The disequilibria are most notable with respect to the 206Pb 204Pb ratios of the minerals. On a NdSr isotopic diagram, the inclusion data plot in a wider area than that for oceanic basalts from a distinctly more depleted component than MORB with higher 143Nd 144Nd and a much broader range of 87Sr 86Sr values, paralleling the theoretical trajectory of a sea-water altered lithosphere in NdSr space. The garnets consistently show lower ?? and ?? values than the pyroxenes and pyroxenites, whereas a phlogopite shows the highest ?? and ?? values among all the minerals and rocks studied. In a plot of ??207 and ??208, the host basalts for all three areas show lower ??207 and higher ??208 values than do the xenoliths, indicating derivation of basalts from Th-rich (relative to U) sources and xenoliths from U-rich sources. The xenolith data trends toward the enriched mantle components, EMI and EMII-like, characterized by high 87Sr 86Sr and ??207 values but with slightly higher 143Nd 144Nd. The EMI trend is shown more distinctly by the host

  4. Arsenic and other oxyanion-forming trace elements in an alluvial basin aquifer: Evaluating sources and mobilization by isotopic tracers (Sr, B, S, O, H, Ra)

    Energy Technology Data Exchange (ETDEWEB)

    Vinson, David S., E-mail: dsv3@duke.edu [Duke University, Division of Earth and Ocean Sciences, Box 90227, Durham, NC 27708 (United States); McIntosh, Jennifer C. [University of Arizona, Department of Hydrology and Water Resources, 1133 E. James E. Rogers Way, Tucson, AZ 85721 (United States); Dwyer, Gary S.; Vengosh, Avner [Duke University, Division of Earth and Ocean Sciences, Box 90227, Durham, NC 27708 (United States)

    2011-08-15

    Highlights: > Elevated natural As and F occur in the Willcox Basin aquifer of Arizona. > Oxyanion-forming elements are derived from volcanic-source aquifer sediments. > Sr isotopes trace sediment sources linked to oxyanion-forming trace elements. > {sup 87}Sr/{sup 86}Sr > 0.720 indicates Proterozoic crystalline-source sediment contributing low As. > Both sediment source and hydrogeochemical evolution (Ca/Na) affect As levels. - Abstract: The Willcox Basin is a hydrologically closed basin in semi-arid southeastern Arizona (USA) and, like many other alluvial basins in the southwestern USA, is characterized by oxic, near-neutral to slightly basic groundwater containing naturally elevated levels of oxyanion-forming trace elements such as As. This study evaluates the sources and mobilization of these oxyanionic trace elements of health significance by using several isotopic tracers of water-rock interaction and groundwater sources ({sup 87}Sr/{sup 86}Sr, {delta}{sup 34}S{sub SO4}, {delta}{sup 11}B, {delta}{sup 2}H, {delta}{sup 18}O, {sup 3}H). Values of {delta}{sup 2}H (-85 per mille to -64 per mille) and {delta}{sup 18}O (-11.8 per mille to -8.6 per mille) are consistent with precipitation and groundwater in adjacent alluvial basins, and low to non-detectable {sup 3}H activities further imply that modern recharge is slow in this semi-arid environment. Large variations in {sup 87}Sr/{sup 86}Sr ratios imply that groundwater has interacted with multiple sediment sources that constitute the basin-fill aquifer, including Tertiary felsic volcanic rocks, Paleozoic sedimentary rocks, and Proterozoic crystalline rocks. In general, low concentrations of oxyanion-forming trace elements and F{sup -} are associated with a group of waters exhibiting highly radiogenic values of {sup 87}Sr/{sup 86}Sr (0.72064-0.73336) consistent with waters in Proterozoic crystalline rocks in the mountain blocks (0.73247-0.75010). Generally higher As concentrations (2-29 {mu}g L{sup -1}), other

  5. A Sr-Nd-Hf isotope characterization of dust source areas in Victoria Land and the McMurdo Sound sector of Antarctica

    Science.gov (United States)

    Blakowski, Molly A.; Aciego, Sarah M.; Delmonte, Barbara; Baroni, Carlo; Salvatore, Maria Cristina; Sims, Kenneth W. W.

    2016-06-01

    Determining the geographical provenance of dust provides crucial insight into the global dust cycle. For the East Antarctic Ice Sheet (EAIS), the importance of Southern hemisphere potential dust sources has been thoroughly investigated using radiogenic isotopes, whereas proximal dust source areas located on the periphery of the ice sheet remain poorly documented from a geochemical standpoint. In this work, we expand the existing isotopic (Srsbnd Nd) catalogue of dust and sand-sized sediments from Victoria Land and the McMurdo Sound sector, and incorporate Hf isotopic data to place additional constraints on dust source identification. The isotopic field for materials considered in this study is characterized by 87Sr/86Sr ratios ranging from 0.703 to 0.783, εNd between -12.01 and 6.36, and εHf from -16.77 to 6.89. As reported in previous works, the data reveal close relationships between Antarctic sediments and distinct parent lithologies; in addition, our findings emphasize the background presence of very fine dusts originating from dominant global sources and regional volcanic activity as barriers to direct source-to-sink comparison of isotopic signatures. Thus, geochemical characterizations of dust sources to the Antarctic ice sheet involving multiple size fractions, including coarser-grained particles more susceptible to short-range transport, can help us to rule out global sources of dust when examining local sediment cores and ice cores.

  6. Sr isotopic composition of gypsic paleosols as a proxy for Neogene forearc uplift in the South America - Nazca plate system at latitudes 19 to 22° S

    Science.gov (United States)

    Cosentino, N. J.; Jordan, T. E.

    2011-12-01

    Quantification of uplift of a continental surface relative to sea level is challenging. The study area comprises the forearc associated with the South America - Nazca plate margin in northern Chile. The Coastal Cordillera (CdlC) is a mountain range 800 to 2300 m in elevation that ends abruptly to the west at the Pacific Ocean, terminated at a 400 m to 1700 m high scarp. The CdlC is formed mainly of Jurassic - Early Cretaceous igneous rocks, the remnants of a Mesozoic magmatic arc. To the east, the Central Depression (CD) is a forearc basin filled with Cenozoic sediments derived from the arc to the east. Arid to hyperarid climate conditions dominated throughout the Neogene. Profiles from rivers draining the CD and cutting through the CdlC are strongly suggestive that at least 1 km of relative surface uplift occurred since 10 Ma. Paleogeographic reconstructions of continental deposits, marine terraces and tilted originally horizontal depositional surfaces in the CdlC constrain surface uplift histories. However, we seek quantitative information about the magnitude as well as ages of uplift, so that numerical models of forearc geodynamics can be tested against uplift history. We are testing a new paleoaltimetry proxy based on the 87Sr/86Sr ratio of gypsum-rich paleosols. Published studies show that modern pedogenic gypsum in the study area is derived from two sources of distinguishable Sr isotopic values; salts precipitate from aerosols in persistent winter marine fogs and dust comes from the weathering of Andean rocks. It has been shown for modern soils that a transect from the coast to the Andes reveals a progressive decline in 87Sr/86Sr, corresponding to the mixing of marine aerosols and weathered dust. Below 1.5 km altitude, the marine signal diminishes as altitude rises. The low mass difference between 87Sr and 86Sr leads to little fractionation by environmental processes, which is ideal for studying the primary marine vs. Andean signal. Because the Neogene strata

  7. Petrogenesis of synorogenic diorite-granodiorite-granite complexes in the Damara Belt, Namibia: Constraints from U-Pb zircon ages and Sr-Nd-Pb isotopes

    Science.gov (United States)

    Jung, S.; Kröner, A.; Hauff, F.; Masberg, P.

    2015-01-01

    The synorogenic Palmental complex (central Damara Belt, Nambia) consists of ca. 545 Ma old quartz diorites and rare granodiorites and ca. 520 Ma-old leucogranites, representing one of the earliest and most primitive phase of crustal plutonism predating the main high-T regional metamorphism. Most quartz diorites and one granodiorite evolved through multistage, polybaric evolutionary processes involving fractionation from a lithospheric mantle-derived melt, followed by fractional crystallization of mainly hornblende, plagioclase and apatite which is shown by decreasing MgO, FeO, CaO, TiO2 and P2O5 with increasing SiO2. Assimilation of felsic basement gneisses was also important during formation of these granitoids. Although their chemical characteristics (high LILE, low HFSE) resemble those of quartz diorites and granodiorites with calc-alkaline affinity, they differ in their enriched Sr (initial 87Sr/86Sr: 0.7061-0.7098) and Nd (initial εNd: -2.7 to -9.9) isotopic composition. Neodymium depleted mantle mean crustal residence ages range from 1.3 to 1.9 Ga for the quartz diorites including the granodiorite. These model ages correlate with major and trace element abundances, further substantiating that AFC processes modified the initial isotopic systematics. Lead (206Pb/204Pb: 17.43-17.68, 207Pb/204Pb: 15.61-15.66, 208Pb/204Pb: 38.19-38.49) isotopic composition are unradiogenic relative to other Damaran intrusive rocks but plot above the Stacey and Kramers (1975) reference line, indicating that the source underwent an ancient (pre Pan-African) increase in U/Pb and Th/U, followed by more recent U-depletion. Some variation in 206Pb/204Pb at high 207Pb/204Pb further indicates involvement of ancient crustal material, most likely through AFC processes. A cross-cutting leucogranite dyke has also evolved isotopic compositions (initial 87Sr/86Sr: 0.7326; initial εNd: -15.6; 206Pb/204Pb: 17.42, 207Pb/204Pb: 15.62, 208Pb/204Pb: 38.16) but in view of the apparent younger age of

  8. Characteristics of Sr, Nd and Pb isotopic compositions of hydrothermal Si-Fe-Mn-oxyhydroxides at the PACMANUS hydrothermal field, Eastern Manus Basin

    Institute of Scientific and Technical Information of China (English)

    YANG Baoju; ZENG Zhigang; WANG Xiaoyuan

    2015-01-01

    Si-Fe-Mn-oxyhydroxides dredged at the PACMANUS (Papua New Guinea–Australia–Canada–Manus) hydrothermal field, Eastern Manus Basin, have87Sr/86Sr=0.708 079–0.708 581;εNd=5.149 833–6.534 826;208Pb/204Pb=38.245–38.440;207Pb/204Pb=15.503–15.560;206Pb/204Pb=18.682–18.783.87Sr/86Sr isotope ratios are relatively homogeneous and close to the value of the surrounding seawater (0.709 16). The content of Sr in the samples contributed by seawater was estimated to be 76.7%–83.1% of total amount. The mixing temperature of hydrothermal fluids and seawater were ranging from 53.2°C to 72.2°C and the hydrothermal activities were unstable when the samples precipitated. TheεNd values of all the samples are positive, which differ from the values of ferromanganese nodules (crusts) with hydrogenic origin. Nd was mainly derived from substrate rocks leached by hydrothermal circulation and preserved the hydrothermal signature. Pb isotopic compositions of most samples show minor variability except Sample #9–2 that has relatively high values of Pb isotopes. The Pb may be derived from the Eastern Manus Basin rocks leached by the hydrothermal fluid. The slightly lower208Pb/204Pb and 207Pb/204Pb values of the samples indicated that the hydrothermal circulation in PACMANUS was not entire and sufficient, or that hydrothermal circulation had transient changes in the past. Si-Fe-Mn-oxyhydroxides in the samples preserved the heterogeneities of local rocks.

  9. U-Pb zircon geochronology, petrochemical and Sr-Nd isotopic characteristic of Late Neoproterozoic granitoid of the Bornaward Complex (Bardaskan-NE Iran)

    Science.gov (United States)

    Bagherzadeh, R. Monazzami; Karimpour, M. H.; Farmer, G. Lang; Stern, C. R.; Santos, J. F.; Rahimi, B.; Heidarian Shahri, M. R.

    2015-11-01

    The Bornaward Granitoid Complex (BGC) in the Taknar Zone is located in the northeast of Central Iranian Block. The BGC consists of granite, alkaligranite, syenogranite, leucogranite, granophyre, monzogranite, granodiorite, tonalite and diorite that have intruded into the center of Taknar Zone. These intrusive rocks affected by low grade metamorphism. Because of there are no reliable isotope dating data, for the Bornaward Granitoid Complex rocks have been proposed discordant ages (Jurassic, Cretaceous or even younger ages) by many studies. In the present study, new isotopic information based on zircon U-Pb dating has revealed the origin and time of the formation of the BGC. These new results do not confirm previously proposed ages. The results obtained from zircon U-Pb dating of the BGC rocks suggest late-Neoproterozoic (Precambrian) age (540-550 Ma). The Bornaward Granitoid Complex is middle-high metaluminous to lower-middle peraluminous and belongs to tholeiite, calc-alkaline to high-K calc-alkaline rock series with enrichment in LIL (Cs, Rb and Ba, U, K, Zr, Y, Th) and depletion in HIL (Sr and Nb, Ta, Ti) elements. Chondrite-normalized Rare Earth Elements (REE) plots indicate minor enrichment of LREE compared to HREE, and strong negative anomaly of Eu compared to other Rare Earth Elements. Furthermore, initial 87Sr/86Sr and 143Nd/144Nd range from 0.70351 to 0.71689 and 0.511585 to 0.512061, respectively, and initial εNd isotope values for granite, granodiorite and diorite range from -6.73 to 2.52. These all indicate that the BGC has derived from partial melting of distinct basement source regions with very high initial 87Sr/86Sr and undergoing extensive crustal contamination (S-type granite).

  10. Nd isotopic disequilibrium be- tween minerals and Rb-Sr age of the secondary phengite in eclogite from the Yangkou area, Qingdao, eastern China

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    There are two generations of white micas in retrograded coesite-bearing eclogite from the Yangkou area near Qingdao, eastern China. The secondary phengite developed along the folliations in eclogite is the majority of the white micas. Nd and Sr isotopic disequilibriums between garnet and retrograded omphacite as well as secondary phengite have been observed. Consequently, the Rb-Sr ages ((193 ± 4) Ma―(195 ± 4) Ma) given by the tie lines of the secondary phengite + garnet or whole rock may predate the formation time of the phengite. The Rb-Sr age of (183 ± 4) Ma given by the secondary phengite + retrograde omphacite is much closer to the formation time of the phengite indicating the retrograde age of eclogite instead of a cooling age of eclogite at 500℃.

  11. Astronomically-Forced Lake Expansion and Contraction Cycles: Sr Isotopic Evidence from the Eocene Green River Formation, Western USA

    Science.gov (United States)

    Baddouh, M.; Meyers, S. R.; Carroll, A.; Beard, B. L.; Johnson, C.

    2014-12-01

    87Sr/86Sr ratio from ancient lake deposits offer a unique insight into the astronomical forcing of lake expansion and contraction, by recording changes in runoff/groundwater provenance. We present new high-resolution 87Sr/86Sr data from the upper Wilkins Peak Member, to investigate linkages between astronomical forcing, water sources, and lake level in a classic rhythmic succession. Fifty-one 87Sr/86Sr ratios from White Mountain core #1 were acquired with a sampling interval of ~30 cm starting from the top of alluvial "I" bed to the lower Laney Member. The 87Sr/86Sr data show a strong and significant negative correlation with oil-yield, a traditional proxy for paleolake level and organic productivity. Application of a radioisotopic time scale, using previously dated ash beds, reveals that both 87Sr/86Sr and oil yield have a strong 20 kyr rhythm. The 87Sr/86Sr data more clearly express a longer period 100 kyr signal, similar to the Laskar 10D eccentricity solution. Using our nominal radioisotopic time scale, the Laskar 10D solution and 87Sr/86Sr data suggest that highest lake levels and greatest organic enrichment are attained during greatest precession and eccentricity. Regional geologic studies and modern river water analyses have shown that less radiogenic waters mostly originate west of the basin, where drainage is strongly influenced by thick Paleozoic and Mesozoic marine carbonate units. Decreased in 87Sr/86Sr therefore imply greater relative water contributions from the Sevier orogenic highlands, relative to lower relief, more radiogenic ranges lying to the east. We therefore propose that highstands of Lake Gosiute record increased penetration of Pacific moisture, related either to increased El Niño frequency or southward displacement of major storm tracks. We hypothesize that the occurrence of wetter winters caused expansion of Lake Gosiute, deposition of organic carbon rich facies, and decreased lake water 87Sr/86Sr.

  12. Man, nutrition and mobility: A comparison of teeth and bone from the Medieval era and the present from Pb and Sr isotopes

    International Nuclear Information System (INIS)

    Naturally occurring isotopic systems, such as strontium (Sr) and lead (Pb), are very useful for characterizing different sources and to produce background information. Norwegian teeth from the Medieval era have 206Pb/204Pb ratios between 18.8 and 18.2, in comparison with present day ratios of between 18.0 and 17.6 showing the impact of Pb from modern industrialization and from traffic. Sr analyses of Medieval teeth show that an individual living in a coastal town on the west coast of Norway can easily be distinguished from one in a rural area at that time. The Sr signature shows that Medieval people lived on local products while present people to a greater degree live on imported or domestic industrially processed food. Medieval and modern teeth from one site give similar Pb signatures and concentrations indicating no increase in pollution over time. However, the impact of industrial pollution can be seen from Pb analyses on contemporary teeth, so that the method can be used to monitor emission of heavy metals from local industry. Whilst the Pb and Sr natural isotopic systems individually provide valuable information, a combination of the two techniques is a very powerful tool in environmental and archaeological research. (Copyright (c) 1998 Elsevier Science B.V., Amsterdam. All rights reserved.)

  13. Sr, Nd isotope geochemistry of volcanic rock series and its geological significance in the middle Okinawa Trough

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    There exists extensive basic-acidic volcanic rock series in the middle section of the Okinawa Trough. Different types of these volcanic rocks have their own average strontium ratios of 0.704 749, 0.705 062, 0.708 771, 0.704 840 and 0.720 301 with average 143Nd/144Nd ratios of 0.512 820, 0.512 673, 0.512 413, 0.512 729 and 0.512 034. These ratios of Sr and Nd isotopes all fall on a theoretic hyperbolic curve of mixing between two end-members of MORB and rhyolitic magma. So we infer that these different kinds of volcanic rocks in the middle Okinawa Trough are the erupted product in different stages of formation and evolution of the trough crust. MORB magma, which had suffered assimilation, mixed with the early-formed crust-derived rhyolitic partial melt mass at different ratios; then, these mixed magma erupted and formed volcanic rock types of the trough. This study indicates that the Okinawa Trough is coming into a stage of submarine spreading from the stage of continental rift.

  14. Sr, Nd isotope geochemistry of volcanic rock series and its geological significance in the middle Okinawa Trough

    Institute of Scientific and Technical Information of China (English)

    孟宪伟; 陈志华; 杜德文; 吴金龙

    2000-01-01

    There exists extensive basic-acidic volcanic rock series in the middle section of the Okinawa Trough. Different types of these volcanic rocks have their own average strontium ratios of 0.704749, 0.705062, 0.708771, 0.704840 and 0.720301 with average 143Nd/144Nd ratios of 0.512 820, 0.512 673, 0.512 413, 0.512 729 and 0.512 034. These ratios of Sr and Nd isotopes all fall on a theoretic hyperbolic curve of mixing between two end-members of MORE and rhyolitic magma. So we infer that these different kinds of volcanic rocks in the middle Okinawa Trough are the erupted product in different stages of formation and evolution of the trough crust. MORE magma, which had suffered assimilation, mixed with the early-formed crust-derived rhyolitic partial melt mass at different ratios; then, these mixed magma erupted and formed volcanic rock types of the trough. This study indicates that the Okinawa Trough is coming into a stage of submarine spreading from the stage of continental rift.

  15. Melt extraction and enrichment processes in the New Caledonia lherzolites: Evidence from geochemical and Sr-Nd isotope data

    Science.gov (United States)

    Secchiari, Arianna; Montanini, Alessandra; Bosch, Delphine; Macera, Patrizia; Cluzel, Dominique

    2016-09-01

    The New Caledonia ophiolite (Peridotite Nappe) is dominated by mantle lithologies, composed of forearc-related refractory harzburgites and minor lherzolites in both the spinel and plagioclase facies. In this study, a comprehensive geochemical data set (major, trace elements and Sr-Nd isotopes) is used to constrain the mantle evolution of the lherzolites and their relationships with the basalts from the Poya Terrane, which tectonically underlies the mantle rocks. The majority of the lherzolites are low-strain porphyroclastic tectonites. They likely record an asthenospheric origin followed by re-equilibration at lithospheric conditions, as supported by geothermometric estimates (T = 1100-940 °C and 920-890 °C for porphyroclastic and neoblastic spinel-facies assemblages, respectively). Olivine composition (Fo = 88.5-90.0 mol%), spinel Cr# ([molar 100 • Cr/(Cr + Al)] = 13-17) and relatively high amounts (7-8 vol%) of Al2O3- and Na2O-rich clinopyroxene (up to 0.5 and 6.5 wt.%, respectively) indicate a moderately depleted geochemical signature for the spinel lherzolites. Bulk rock and clinopyroxene rare earth elements (REE) patterns display a typical abyssal-type signature, i.e. steeply plunging LREE accompanied by nearly flat HREE to MREE. Clinopyroxene REE compositions of the spinel lherzolites may be reproduced by small amounts of fractional melting of a garnet lherzolite precursor (~ 4%), followed by 4%-5% melting in the spinel peridotite field. The plagioclase lherzolites show melt impregnation microstructures, Cr- and Ti-rich spinels and incompatible trace element enrichments (REE, Ti, Y, and Zr) in bulk rocks and clinopyroxenes. Impregnation modelling for these elements suggests that the plagioclase lherzolites originated from residual spinel lherzolites by entrapment of highly depleted (non-aggregated) MORB melt fractions in the shallow oceanic lithosphere. Nd isotope compositions of the investigated peridotites are consistent with derivation from an

  16. Multi-Isotopic (o, H, Sr, Li) Tracing of the Fluxes Involved in the Water Status of a Peatland (la Sauvetat, Massif Central, France)

    Science.gov (United States)

    Agnès, B.; Negrel, P. J.; Millot, R.; Clotilde, B.

    2010-12-01

    The bio-diversity (vegetation and fauna) of peatlands, like all wetlands ecosystems, are strongly fragile as they are requiring very specific wet conditions. In the past 20 years, increasing efforts were engaged to restore degraded wetlands, to create new wetlands where they have been totally lost and to manage wetlands sustainably in order to assess their multiple benefits. However, engaging specific actions to restore and preserve wetlands require an important knowledge on the water cycle in such systems. In this study, we propose to use chemical and multi-isotopic approaches combined with hydrological measurements (piezometric level and stream flow measurements) to trace the fluxes of water and dissolved element involved in the “Narces de la Sauvetat” peatland (France) and for the stream draining the area. Aims are to evaluate the water status of this ecosystem as well as the origin of dissolved elements and possible anthropogenic impacts. These approaches clearly demonstrated their effectiveness to improve the knowledge on the hydrological functioning of wetlands ecosystems. Main results are (1) at least three fluxes with distinct chemical and isotopic signatures are providing water supplies to peatland (Sr and stable isotopes), (2) water flow that comes out of the peatland through the stream is certainly negligible (Li isotopes) and 3) water within the peat land exhibits Sr and Li -isotopes values consistent with carbonate amendments inputs used in local agriculture. The outcomes of this study are that peatland ecosystem water balance is poorly affected by its outlet but are strongly controlled by groundwater replenishment. This could lead to a better adjustment of decision maker choices to maintain the water balance of the peatland, which is essential for the preservation of this fragile ecosystem. This study also opens a new field for Li isotope investigations in hydro-systems and highlights the possibility of using Li isotopes as environmental tracers.

  17. Coral Sr-U thermometry

    Science.gov (United States)

    DeCarlo, Thomas M.; Gaetani, Glenn A.; Cohen, Anne L.; Foster, Gavin L.; Alpert, Alice E.; Stewart, Joseph A.

    2016-06-01

    Coral skeletons archive past climate variability with unrivaled temporal resolution. However, extraction of accurate temperature information from coral skeletons has been limited by "vital effects," which confound, and sometimes override, the temperature dependence of geochemical proxies. We present a new approach to coral paleothermometry based on results of abiogenic precipitation experiments interpreted within a framework provided by a quantitative model of the coral biomineralization process. DeCarlo et al. (2015a) investigated temperature and carbonate chemistry controls on abiogenic partitioning of Sr/Ca and U/Ca between aragonite and seawater and modeled the sensitivity of skeletal composition to processes occurring at the site of calcification. The model predicts that temperature can be accurately reconstructed from coral skeleton by combining Sr/Ca and U/Ca ratios into a new proxy, which we refer to hereafter as the Sr-U thermometer. Here we test the model predictions with measured Sr/Ca and U/Ca ratios of 14 Porites sp. corals collected from the tropical Pacific Ocean and the Red Sea, with a subset also analyzed using the boron isotope (δ11B) pH proxy. Observed relationships among Sr/Ca, U/Ca, and δ11B agree with model predictions, indicating that the model accounts for the key features of the coral biomineralization process. By calibrating to instrumental temperature records, we show that Sr-U captures 93% of mean annual temperature variability (26-30°C) and has a standard deviation of prediction of 0.5°C, compared to 1°C using Sr/Ca alone. The Sr-U thermometer may offer significantly improved reliability for reconstructing past ocean temperatures from coral skeletons.

  18. Geochemical and C, O, Sr, and U-series isotopic evidence for the meteoric origin of calcrete at Solitario Wash, Crater Flat, Nevada, USA

    Science.gov (United States)

    Neymark, L. A.; Paces, J. B.; Marshall, B. D.; Peterman, Z. E.; Whelan, J. F.

    2005-08-01

    Calcite-rich soils (calcrete) in alluvium and colluvium at Solitario Wash, Crater Flat, Nevada, USA, contain pedogenic calcite and opaline silica similar to soils present elsewhere in the semi-arid southwestern United States. Nevertheless, a ground-water discharge origin for the Solitario Wash soil deposits was proposed in a series of publications proposing elevation-dependent variations of carbon and oxygen isotopes in calcrete samples. Discharge of ground water in the past would raise the possibility of future flooding in the unsaturated zone at Yucca Mountain, Nevada, site of a proposed high-level nuclear waste repository. New geochemical and carbon, oxygen, strontium, and uranium-series isotopic data disprove the presence of systematic elevation-isotopic composition relations, which are the main justification given for a proposed ground-water discharge origin of the calcrete deposits at Solitario Wash. Values of δ13C (-4.1 to -7.8 per mil [‰]), δ18O (23.8-17.2‰), 87Sr/86Sr (0.71270-0.71146), and initial 234U/238U activity ratios of about 1.6 in the new calcrete samples are within ranges previously observed in pedogenic carbonate deposits at Yucca Mountain and are incompatible with a ground-water origin for the calcrete. Variations in carbon and oxygen isotopes in Solitario Wash calcrete likely are caused by pedogenic deposition from meteoric water under varying Quaternary climatic conditions over hundreds of thousands of years.

  19. Geochemistry and Nd Sr isotopic studies of Late Mesozoic granitoids in the southeastern Hubei Province, Middle Lower Yangtze River belt, Eastern China: Petrogenesis and tectonic setting

    Science.gov (United States)

    Xie, Guiqing; Mao, Jingwen; Li, Ruiling; Bierlein, Frank P.

    2008-08-01

    A geochemical and isotopic study was carried out for the Mesozoic Yangxin, Tieshan and Echeng granitoid batholiths in the southeastern Hubei Province, eastern China, in order to constrain their petrogenesis and tectonic setting. These granitoids dominantly consist of quartz diorite, monzonite and granite. They are characterized by SiO 2 and Na 2O compositions of between 54.6 and 76.6 wt.%, and 2.9 to 5.6 wt.%, respectively, enrichment in light rare earth elements (LREE) and large ion lithophile elements (LILE), and relative depletion in Y (concentrations ranging from 5.17 to 29.3 ppm) and Yb (0.34-2.83 ppm), with the majority of the granitoids being geochemically similar to high-SiO 2 adakites (HSA). Their initial Nd ( ɛNd = - 12.5 to - 6.1) and Sr (( 87Sr/ 86Sr) i = 0.7054-0.7085) isotopic compositions, however, distinguish them from adakites produced by partial melting of subducted slab and those produced by partial melting of the lower crust of the Yangtze Craton in the Late Mesozoic. The granitoid batholiths in the southeastern Hubei Province exhibit very low MgO ranging from 0.09 to 2.19 wt.% with an average of 0.96 wt.%, and large variations in negative to positive Eu anomalies (Eu/Eu * = 0.22-1.4), especially the Tieshan granites and Yangxin granite porphyry (Eu/Eu * = 0.22-0.73). Geochemical and Nd-Sr isotopic data demonstrate that these granitoids originated as partial melts of an enriched mantle source that experienced significant contamination of lower crust materials and fractional crystallization during magma ascent. Late Mesozoic granitoids in the southeastern Hubei Province of the Middle-Lower Yangtze River belt were dominantly emplaced in an extensional tectonic regime, in response to basaltic underplating, which was followed by lithospheric thinning during the early Cretaceous.

  20. Sr-Nd isotope geochemistry and tectonomagmatic setting of the Dehsalm Cu-Mo porphyry mineralizing intrusives from Lut Block, eastern Iran

    Science.gov (United States)

    Arjmandzadeh, R.; Santos, J. F.

    2014-01-01

    The Dehsalm Cu-Mo-bearing porphyritic granitoids belong to the Lut Block volcanic-plutonic belt (central eastern Iran). These rocks range in composition from gabbro-diorite to granite, with dominance of monzonites and quartz monzonites, and have geochemical features of high-K calc-alkaline to shoshonitic volcanic arc suites. Primitive mantle-normalized trace element spider diagrams display strong enrichment in large-ion lithophile elements such as Rb, Ba and Cs and depletions in some high-field strength elements, e.g., Nb, Ti, Y and HREE. Chondrite-normalized plots display significant LREE enrichments, high LaN/YbN and a lack of Eu anomaly. High Sr/Y and La/Yb ratios of Dehsalm intrusives reveal that, despite their K-rich composition, these granitoids show some resemblances with adakitic rocks. A Rb-Sr whole rock-feldspar-biotite age of 33 ± 1 Ma was obtained in a quartz monzonite sample and coincides, within error, with a previous geochronological result in Chah-Shaljami granitoids, further northwest within the Lut Block. (87Sr/86Sr)i and ɛNdi isotopic ratios range from 0.70481 to 0.70508 and from +1.5 to +2.5, respectively, which fits into a supra-subduction mantle wedge source for the parental melts and indicates that crustal contribution for magma diversification was of limited importance. Sr and Nd isotopic compositions together with major and trace element geochemistry point to an origin of the parental magmas by melting of a metasomatized mantle source, with phlogopite breakdown playing a significant role in the geochemical fingerprints of the parental magmas; small amounts of residual garnet in the mantle source also help to explain some trace element patterns. Geochemical features of Dehsalm porphyries and its association with Cu-Mo mineralization agree with a mature continental arc setting related to the convergence of Afghan and Lut plates during Oligocene.

  1. Accurate experimental determination of the isotope effects on the triple point temperature of water. I. Dependence on the 2H abundance

    Science.gov (United States)

    Faghihi, V.; Peruzzi, A.; Aerts-Bijma, A. T.; Jansen, H. G.; Spriensma, J. J.; van Geel, J.; Meijer, H. A. J.

    2015-12-01

    Variation in the isotopic composition of water is one of the major contributors to uncertainty in the realization of the triple point of water (TPW). Although the dependence of the TPW on the isotopic composition of the water has been known for years, there is still a lack of a detailed and accurate experimental determination of the values for the correction constants. This paper is the first of two articles (Part I and Part II) that address quantification of isotope abundance effects on the triple point temperature of water. In this paper, we describe our experimental assessment of the 2H isotope effect. We manufactured five triple point cells with prepared water mixtures with a range of 2H isotopic abundances encompassing widely the natural abundance range, while the 18O and 17O isotopic abundance were kept approximately constant and the 18O  -  17O ratio was close to the Meijer-Li relationship for natural waters. The selected range of 2H isotopic abundances led to cells that realised TPW temperatures between approximately  -140 μK to  +2500 μK with respect to the TPW temperature as realized by VSMOW (Vienna Standard Mean Ocean Water). Our experiment led to determination of the value for the δ2H correction parameter of A2H  =  673 μK / (‰ deviation of δ2H from VSMOW) with a combined uncertainty of 4 μK (k  =  1, or 1σ).

  2. In situ Sr isotope analysis of apatite by LA-MC-ICPMS: constraints on the evolution of ore fluids of the Yinachang Fe-Cu-REE deposit, Southwest China

    Science.gov (United States)

    Zhao, Xin-Fu; Zhou, Mei-Fu; Gao, Jian-Feng; Li, Xiao-Chun; Li, Jian-Wei

    2015-10-01

    Apatite is a ubiquitous accessory mineral in a variety of rocks and hydrothermal ores. Strontium isotopes of apatite are well known to retain petrogenetic information and have been widely used to investigate the origin of igneous rocks, but such attempts have rarely been made to constrain ore-forming processes of hydrothermal systems. We here report in situ LA-MC-ICPMS Sr isotope data of apatite from the ~1660-Ma Yinachang Fe-Cu-REE deposit, Southwest China. The formation of this deposit was coeval to the emplacement of regionally distributed doleritic intrusions within a continental-rift setting. The deposit has a paragenetic sequence consisting of sodic alteration (stage I), magnetite mineralization (stage II), Cu sulfide and REE mineralization (stage III), and final barren calcite veining (stage IV). The stage II and III assemblages contain abundant apatite, allowing to investigate the temporal evolution of the Sr isotopic composition of the ore fluids. Apatite of stage II (Apt II) is associated with fluorite, magnetite, and siderite, whereas apatite from stage III (Apt III) occurs intimately intergrown with ankerite and Cu sulfides. Apt II has 87Sr/86Sr ratios varying from 0.70377 to 0.71074, broadly compatible with the coeval doleritic intrusions (0.70592 to 0.70692), indicating that ore-forming fluids responsible for stage II magnetite mineralization were largely equilibrated with mantle-derived mafic rocks. In contrast, Apt III has distinctly higher 87Sr/86Sr ratios from 0.71021 to 0.72114, which are interpreted to reflect external radiogenic Sr, likely derived from the Paleoproterozoic strata. Some Apt III crystals have undergone extensive metasomatism indicated by abundant monazite inclusions. The metasomatized apatite has much higher 87Sr/86Sr ratios up to 0.73721, which is consistent with bulk-rock Rb-Sr isotope analyses of Cu ores with 87Sr/86Sri from 0.71906 to 0.74632. The elevated 87Sr/86Sr values of metasomatized apatite and bulk Cu ores indicate

  3. Elemental geochemistry and Sr-Nd isotopic fingerprinting of sediments in monsoon dominated river systems along the west coast of India.

    Science.gov (United States)

    Pradhan, S. U.; Zhang, J.; Baskaran, M. M.; Shirodkar, P.; Wu, Y.

    2014-12-01

    Strontium-Neodymium isotopes have been widely utilized as provenance tracers of major global river basins. Using HR-ICPMS (elements) and MC-ICPMS (isotopes), we measured a suite of trace elements, 87Sr/86Sr and 143Nd/144Nd isotopic ratios from silicate (Si) and carbonate (CO32-) fractions of 37 bottom sediment samples during 3 seasons along a transect from the estuary upstream in Narmada (ND) and Netravati (NT), the two large rivers along the west coast of India, discharge into the Arabian Sea. Strontium isotopic values ranged from 0.70910 to 0.71778 (NR CO32-), 0.71014 to 0.72427 (NT CO32-) and 0.71085 to 0.72825 (NR Si), and 0.71025 to 0.73349 (NT Si). The ɛNd(0) values ranged from -22.1 to -0.8 (NR CO32-), and -32.2 to -24.3 (NT, CO32-), and -23.7 to -6.2 (NR Si) and -37.4 to -21.2 (NT Si). Variable extents of seasonal and spatial variations on the isotopic compositions of Sr and Nd (both in CO32- and Si fractions), were observed in both rivers. A comparison of the 'model age' of the sediments calculated from the time-depleted-mantle (TDM) model using the concentrations of Nd and Sm and isotopic composition of Nd indicate the following: i) For NT, the TDM-based 'model age', 2.8 to 3.3 Ga, agrees with the age of Peninsular Gneiss, an older gneissic complex (3.2-3.4 Ga) found in this watershed; ii) For NR, there is discordance between the TDM-based 'model age' (1.3-2.4 Ga) and the age of the rocks in this watershed (Deccan basalt, ~65 Ma). We attribute this discordance to mixing of older material from the Precambrian rocks derived by weathering at the head waters of NR. From the observed differences in the Sr isotopes in the main stream and tributaries, we estimate that ~90% of the sediments are derived from main stream and ~10% is derived from tributaries using binary mixing equation in NT and additional sediment source(s) in NR. The Sr isotopic signatures of carbonate fractions in both rivers are close to the global average modern seawater (0.7092) and river

  4. Major element, REE, and Pb, Nd and Sr isotopic geochemistry of Cenozoic volcanic rocks of eastern China: implications for their origin from suboceanic-type mantle reservoirs

    Science.gov (United States)

    Basu, A.R.; Wang, Junwen; Huang, Wankang; Xie, Guanghong; Tatsumoto, M.

    1991-01-01

    Major- and rare-earth-element (REE) concentrations and UThPb, SmNd, and RbSr isotope systematics are reported for Cenozoic volcanic rocks from northeastern and eastern China. These volcanic rocks, characteristically lacking the calc-alkaline suite of orogenic belts, were emplaced in a rift system which formed in response to the subduction of the western Pacific plate beneath the eastern Asiatic continental margin. The rocks sampled range from basanite and alkali olivine basalt, through olivine tholeiite and quartz tholeiite, to potassic basalts, alkali trachytes, pantellerite, and limburgite. These rock suites represent the volcanic centers of Datong, Hanobar, Kuandian, Changbaishan and Wudalianchi in northeastern China, and Mingxi in the Fujian Province of eastern China. The major-element and REE geochemistry is characteristic of each volcanic suite broadly evolving through cogenetic magmatic processes. Some of the outstanding features of the isotopic correlation arrays are as follows: (1) NdSr shows an anticorrelation within the field of ocean island basalts, extending from the MORB end-member to an enriched, time-averaged high Rb Sr and Nd Sr end-member (EM1), (2) SrPb also shows an anticorrelation, similar to that of Hawaiian and walvis Ridge basalts, (3) NdPb shows a positive correlation, and (4) the 207Pb 204Pb vs 206Pb 204Pb plot shows linear arrays parallel to the general trend (NHRL) for MORB on both sides of the geochron, although in the 208Pb 204Pb vs 206Pb 204Pb plot the linear array is significantly displaced above the NHRL in a pattern similar to that of the oceanic island basalts that show the Dupal signatures. In all isotope correlation patterns, the data arrays define two different mantle components-a MORB-like component and an enriched mantle component. The isotopic data presented here clearly demonstrate the existence of Dupal compositions in the sources of the continental volcanic rocks of eastern China. We suggest that the subcontinental mantle

  5. A late Miocene-early Pliocene chain of lakes fed by the Colorado River: Evidence from Sr, C, and O isotopes of the Bouse Formation and related units between Grand Canyon and the Gulf of California

    Science.gov (United States)

    Roskowski, J.A.; Patchett, P.J.; Spencer, J.E.; Pearthree, P.A.; Dettman, D.L.; Faulds, J.E.; Reynolds, A.C.

    2010-01-01

    We report strontium isotopic results for the late Miocene Hualapai Limestone of the Lake Mead area (Arizona-Nevada) and the latest Miocene to early Pliocene Bouse Formation and related units of the lower Colorado River trough (Arizona-California-Nevada), together with parallel oxygen and carbon isotopic analyses of Bouse samples, to constrain the lake-overflow model for integration of the Colorado River. Sr iso topic analyses on the basal 1-5 cm of marl, in particular along a transect over a range of altitude in the lowest-altitude basin that contains freshwater, brackish, and marine fossils, document the 87Sr/86Sr of first-arriving Bouse waters. Results reinforce the similarity between the 87Sr/86Sr of Bouse Formation carbonates and present-day Colorado River water, and the systematic distinction of these values from Neogene marine Sr. Basal Bouse samples show that 87Sr/86Sr decreased from 0.7111 to values in the range 0.7107-0.7109 during early basin filling. 87Sr/86Sr values from a recently identified marl in the Las Vegas area are within the range of Bouse Sr ratios. 87Sr/86Sr values from the Hualapai Limestone decrease upsection from 0.7195 to 0.7137, in the approach to a time soon after 6 Ma when Hualapai deposition ceased and the Colorado River became established through the Lake Mead area. Bouse Formation ??18O values range from -12.9??? to +1.0??? Vienna Pee Dee belemnite (VPDB), and ??13C between -6.5??? and +3.4??? VPDB. Negative ??18O values appear to require a continental origin for waters, and the trend to higher ??18O suggests evaporation in lake waters. Sr and stable isotopic results for sectioned barnacle shells and from bedding planes of the marine fish fossil Colpichthys regis demonstrate that these animals lived in saline freshwater, and that there is no evidence for incursions of marine water, either long-lived or brief in duration. Lack of correlation of Sr and O isotopic variations in the same samples also argue strongly against systematic

  6. Sources of granite magmatism in the Embu Terrane (Ribeira Belt, Brazil): Neoproterozoic crust recycling constrained by elemental and isotope (Sr-Nd-Pb) geochemistry

    Science.gov (United States)

    Alves, Adriana; Janasi, Valdecir de Assis; Campos Neto, Mario da Costa

    2016-07-01

    Whole rock elemental and Sr-Nd isotope geochemistry and in situ K-feldspar Pb isotope geochemistry were used to identify the sources involved in the genesis of Neoproterozoic granites from the Embu Terrane, Ribeira Belt, SE Brazil. Granite magmatism spanned over 200 Ma (810-580 Ma), and is dominated by crust-derived relatively low-T (850-750 °C, zircon saturation) biotite granites to biotite-muscovite granites. Two Cryogenian plutons show the least negative εNdt (-8 to -10) and highest mg# (30-40) of the whole set. Their compositions are strongly contrasted, implying distinct sources for the peraluminous (ASI ∼ 1.2) ∼660 Ma Serra do Quebra-Cangalha batholith (metasedimentary rocks from relatively young upper crust with high Rb/Sr and low Th/U) and the metaluminous (ASI = 0.96-1.00) ∼ 630 Ma Santa Catarina Granite. Although not typical, the geochemical signature of these granites may reflect a continental margin arc environment, and they could be products of a prolonged period of oceanic plate consumption started at ∼810 Ma. The predominant Ediacaran (595-580 Ma) plutons have a spread of compositions from biotite granites with SiO2 as low as ∼65% (e.g., Itapeti, Mauá, Sabaúna and Lagoinha granites) to fractionated muscovite granites (Mogi das Cruzes, Santa Branca and Guacuri granites; up to ∼75% SiO2). εNdT are characteristically negative (-12 to -18), with corresponding Nd TDM indicating sources with Paleoproterozoic mean crustal ages (2.0-2.5 Ga). The Guacuri and Santa Branca muscovite granites have the more negative εNdt, highest 87Sr/86Srt (0.714-0.717) and lowest 208Pb/206Pb and 207Pb/206Pb, consistent with an old metasedimentary source with low time-integrated Rb/Sr. However, a positive Nd-Sr isotope correlation is suggested by data from the other granites, and would be consistent with mixing between an older source predominant in the Mauá granite and a younger, high Rb/Sr source that is more abundant in the Lagoinha granite sample. The

  7. Stable isotope labeling by amino acids in cell culture, SILAC, as a simple and accurate approach to expression proteomics

    DEFF Research Database (Denmark)

    Ong, S.E.; Blagoev, B.; Kratchmarova, I.;

    2002-01-01

    . Here we describe a method, termed SILAC, for stable isotope labeling by amino acids in cell culture, for the in vivo incorporation of specific amino acids into all mammalian proteins. Mammalian cell lines are grown in media lacking a standard essential amino acid but supplemented with a non......Quantitative proteomics has traditionally been performed by two-dimensional gel electrophoresis, but recently, mass spectrometric methods based on stable isotope quantitation have shown great promise for the simultaneous and automated identification and quantitation of complex protein mixtures......-radioactive, isotopically labeled form of that amino acid, in this case deuterated leucine (Leu-d3). We find that growth of cells maintained in these media is no different from growth in normal media as evidenced by cell morphology, doubling time, and ability to differentiate. Complete incorporation of Leu-d3 occurred...

  8. Phase equilibria constraints on liquid lines of descent generated by paired assimilation and fractional crystallization: Trace elements and Sr and Nd isotopes

    International Nuclear Information System (INIS)

    Utilizing a phase equilibria based trace element isotope model for low pressure igneous differentiation, it is now possible to update the methods presently being used to evaluate the effect of assimilation and fractional crystallization (AFC) processes. The results of the calculations presented here indicate that bulk partition coefficients (D) for Sr and Nd are strongly dependent on the chemistry of the assimilants will increase bulk D for network-modifying cations because of the positive correlation of most trace element partition coefficients with reciprocal temperature, and the amount of network forming components in the melt. In addition to the effect of temperature and melt composition, the addition of a magma of different composition from the magma chamber will generally cause a change in the fractionating mineral proportions. For example, a peraluminous assimilant will increase the proportion of plagioclase, and a peralkaline assimilant will increase the proportion of augite. This will in turn have an effect on bulk D. For most multiply saturated mafic to intermediate systems differentiating at low pressure, bulk DSr is >1, and bulk DNd is Sr away from 1 and a peralkaline assimilant drives bulk DNd toward 1. Compared to the results derived in this study, existing models using fixed bulk Ds calculated from closed system conditions will generate results that underestimate the assimilation rate, 87/86Sr and bulk Sr content for a peraluminous assimilant, and over-estimate the assimilation rate, 143/144Nd and Nd content of the assimilant for a peralkaline assimilant

  9. Geochemistry and Sr-Nd isotopic compositions of mantle xenoliths from the Monte Vulture carbonatite-melilitite volcano, central southern Italy

    Science.gov (United States)

    Downes, H.; Kostoula, T.; Jones, A. P.; Beard, A. D.; Thirlwall, M. F.; Bodinier, J.-L.

    2002-08-01

    Spinel peridotite xenoliths found in the Monte Vulture carbonatite-melilitite volcano have been derived from the subcontinental lithospheric mantle beneath central southern Italy. Clinopyroxene-poor lherzolites and harzburgites are the most common rock types, with subordinate wehrlites and dunites. Small quantities of phlogopite and carbonate are present in a few samples. The peridotites record a large degree of partial melting and have experienced subsequent enrichment which has increased their LILE and LREE contents, but in most cases their HFSE contents are low. Despite being carried to the surface by a carbonatite-melilitite host, the whole-rock and clinopyroxene compositions of the xenoliths have a trace-element signature more closely resembling that of silicate-melt metasomatised mantle rather than carbonatite-metasomatised peridotites. 87Sr/86Sr and 143Nd/144Nd isotopic ratios for clinopyroxene from the Vulture peridotites are 0.7042-0.7058 and 0.51260-0.5131 respectively. They form a trend away from the depleted mantle to the composition of the host magmas, and show a significant enrichment in 87Sr/86Sr compared with most European mantle samples. The mantle beneath Monte Vulture has had a complex evolution - we propose that the lithosphere had already undergone extensive partial melting before being affected by metasomatism from a silicate melt which may have been subduction-related.

  10. A combined Sm-Nd, Rb-Sr, and U-Pb isotopic study of Mg-suite norite 78238: Further evidence for early differentiation of the Moon

    Energy Technology Data Exchange (ETDEWEB)

    Edmunson, J; E.Borg, L; Nyquist, L E; Asmerom, Y

    2008-11-17

    Lunar Mg-suite norite 78238 was dated using the Sm-Nd, Rb-Sr, and U-Pb isotopic systems in order to constrain the age of lunar magma ocean solidification and the beginning of Mg-suite magmatism, as well as to provide a direct comparison between the three isotopic systems. The Sm-Nd isotopic system yields a crystallization age for 78238 of 4334 {+-} 37 Ma and an initial {var_epsilon}{sub Nd}{sup 143} value of -0.27 {+-} 0.74. The age-initial {var_epsilon}{sub Nd}{sup 143} (T-I) systematics of a variety of KREEP-rich samples, including 78238 and other Mg-suite rocks, KREEP basalts, and olivine cumulate NWA 773, suggest that lunar differentiation was completed by 4492 {+-} 61 Ma assuming a Chondritic Uniform Reservoir bulk composition for the Moon. The Rb-Sr isotopic systematics of 78238 were disturbed by post-crystallization processes. Nevertheless, selected data points yield two Rb-Sr isochrons. One is concordant with the Sm-Nd crystallization age, 4366 {+-} 53 Ma. The other is 4003 {+-} 95 Ma and is concordant with an Ar-Ar age for 78236. The {sup 207}Pb-{sup 206}Pb age of 4333 {+-} 59 Ma is concordant with the Sm-Nd age. The U-Pb isotopic systematics of 78238 yield linear arrays equivalent to younger ages than the Pb-Pb system, and may reflect fractionation of U and Pb during sample handling. Despite the disturbed nature of the U-Pb systems, a time-averaged {mu} ({sup 238}U/{sup 204}Pb) value of the source can be estimated at 27 {+-} 30 from the Pb-Pb isotopic systematics. Because KREEP-rich samples are likely to be derived from source regions with the highest U/Pb ratios, the relatively low {mu} value calculated for the 78238 source suggests the bulk Moon does not have an exceedingly high {mu} value.

  11. Syn-orogenic high-temperature crustal melting: Geochronological and Nd-Sr-Pb isotope constraints from basement-derived granites (Central Damara Orogen, Namibia)

    Science.gov (United States)

    Ostendorf, Jörg; Jung, Stefan; Berndt-Gerdes, Jasper; Hauff, Folkmar

    2014-04-01

    Major and trace element and Nd, Sr and Pb isotope data from c. 550 Ma-old gray granites and c. 510 Ma-old red leucogranites of the high-grade central part of the Damara orogen (Namibia) indicate a dominantly deep crustal origin. Moderately peraluminous gray granites are isotopically evolved (initial ɛNd: c. - 17) and were likely derived from meta-igneous sources with late Archean to Paleoproterozoic crustal residence ages. Based on a comparison with experimental results, the granites were derived by partial melting of a granodioritic biotite gneiss at c. 900-950 °C and less than 10 kbar. Slightly peraluminous red leucogranites are also isotopically evolved (initial ɛNd: - 15 to - 18) but have undergone extensive crystal fractionation coupled with minor contamination of mid crustal meta-pelitic material. Major and trace element data do not support closed-system fractional crystallization processes for all samples, however, some chemical features underline the importance of crystal fractionation processes especially for the leucogranites. Isotope data do not support mixing of different crust-derived melts or assimilation of crustal rocks by a mafic magma on a large scale. For the gray granites, unradiogenic Pb isotope compositions with substantial variation in 207Pb/204Pb at almost constant 206Pb/204Pb, strongly negative ɛNd values and moderately radiogenic Sr isotope compositions argue for an undepleted nature of the source. High Rb/Sr ratios of the red leucogranites permit a comparison with the gray granites but similar initial ɛNd values indicate that the source of these granites is not fundamentally different to the source of the gray granites. The most acceptable model for both granite types involves partial melting of meta-igneous basement rocks of Archean to Proterozoic age. The consistency of the chemical data with a crustal anatectic origin and the observation that the gray granites intruded before the first peak of high-grade regional metamorphism

  12. Inferences on sediment provenance and source weathering using major, trace and Sr-Nd isotopic compositional variations in alluvial sediments from Sirhind, Punjab, India

    Science.gov (United States)

    Paul, D.; Amir, M.; Sinha, R.; Singh, A.; Balakrishnan, S.

    2013-12-01

    Variations in major oxides and selected trace element concentrations, and Sr and Nd isotope ratios in sediments from two ~45m long cores drilled on the trace of a paleochannel near Sirhind, Sutlej plains, are used to characterize sediment provenance and source weathering vis-à-vis climate change. Drill core lithostratigraphy shows slit/clay layers down to a depth of 4m, and coarse to fine channel-sand bodies between ~4 and ~45m, occasionally interspersed by thin slity-clay layers. OSL ages of three samples constrain an age of 15.8 Ka at ~10m depth, corresponding to post Last Glacial Maximum (LGM) period. Major elemental abundances in de-carbonated bulk sediments (44 samples) fall within the range of surface sediments of present-day rivers sourced in the Himalayas. Strong positive correlations (R2>0.8) of Al2O3 (8.7-19.3 wt%) with K2O (2.23-4.03), MgO (0.49-2.72), Fe2O3 (0.89-7.21) and TiO2 (0.35-0.95), and negative correlation (R2=0.95) with SiO2 (62.5-83.7 wt%) are observed. Fe2O3/K2O ratio in these sediments suggest that sands are chemically immature and dominantly arkosic. A-CN-K plot reveals a weathering trend towards illite running parallel to the A-CN line, indicating weak to moderate weathering at source; similar conclusion is drawn from the chemical index of alternation (CIA) values ranging between 54 and 79. The Cr/Th ratios as well as the La-Th-Sc ternary plot suggest that sediments are dominantly derived from granitic to granodioritic sources. The radiogenic Sr-Nd isotopic composition in 18 samples from one drill-core shows range of values (87Sr/86Sr: 0.7409-0.7946; ɛNd: -23.2 to -15) similar to those of silicate rocks from the Higher and Lesser Himalaya, and the down-core variation pattern is similar to that reported for the Ganga-Yamuna interfluve sediments of similar age1. Down-core variations in 87Sr/86Sr and ɛNd reflect mixing of varying proportions of Higher and Lesser Himalayan sediments, the two dominant sources to the core site. Holocene

  13. Onset of collectivity in neutron-rich Sr and Kr isotopes: Prompt spectroscopy after Coulomb excitation at REX-ISOLDE, CERN

    Directory of Open Access Journals (Sweden)

    Clément E.

    2013-12-01

    Full Text Available A rapid onset of quadrupole deformation is known to occur around the neutron number 60 in the neutron-rich Zr and Sr isotopes. This shape change has made the neutron-rich A = 100 region an active area of experimental and theoretical studies for many decades now. We report in this contribution new experimental results in the neutron rich 96,98Sr investigated by safe Coulomb excitation of radioactive beams at the REX-ISOLDE facility, CERN. Reduced transition probabilities and spectroscopic quadrupole moments have been extracted from the differential Coulomb excitation cross section supporting the scenario of shape coexistence/change at N = 60. Future perspectives are presented including the recent experimental campaign performed at ILL-Grenoble.

  14. Accurate determination of Curium and Californium isotopic ratios by inductively coupled plasma quadrupole mass spectrometry (ICP-QMS) in 248Cm samples for transmutation studies

    International Nuclear Information System (INIS)

    The French Atomic Energy Commission has carried out several experiments including the mini-INCA (INcineration of Actinides) project for the study of minor-actinide transmutation processes in high intensity thermal neutron fluxes, in view of proposing solutions to reduce the radiotoxicity of long-lived nuclear wastes. In this context, a Cm sample enriched in 248Cm (∼97 %) was irradiated in thermal neutron flux at the High Flux Reactor (HFR) of the Laue-Langevin Institute (ILL). This work describes a quadrupole ICP-MS (ICP-QMS) analytical procedure for precise and accurate isotopic composition determination of Cm before sample irradiation and of Cm and Cf after sample irradiation. The factors that affect the accuracy and reproducibility of isotopic ratio measurements by ICP-QMS, such as peak centre correction, detector dead time, mass bias, abundance sensitivity and hydrides formation, instrumental background, and memory blank were carefully evaluated and corrected. Uncertainties of the isotopic ratios, taking into account internal precision of isotope ratio measurements, peak tailing, and hydrides formations ranged from 0.3% to 1.3%. This uncertainties range is quite acceptable for the nuclear data to be used in transmutation studies.

  15. Petrological and Sr-Nd-Os isotopic constraints on the origin of the Fanshan ultrapotassic complex from the North China Craton

    Science.gov (United States)

    Niu, Xiaolu; Chen, Bin; Liu, Ankun; Suzuki, K.; Ma, Xu

    2012-09-01

    The Fanshan ultramafic-syenitic complex is located on the northern margin of North China Craton, with zircon U-Pb ages of 220 Ma. It is a concentrically zoned complex, with syenite in the core, surrounded by ultramafic rocks (clinopyroxenite, glimmerite) and garnet-clinopyroxene syenite, respectively, towards the rim. Diopside, biotite, orthoclase, melanite, magnetite and apatite are the major minerals, with subordinate sphene and calcite. Mineralogy, petrology and geochemical studies point to the formation of the complex through fractional crystallization and accumulation from a SiO2-undersaturated ultrapotassic alkaline-peralkaline parent magma that is characterized by high CaO, Fe2O3, K2O and fluid compositions (P2O5, CO2, H2O, F), and by high temperature and high oxygen fugacity. Rocks from the complex are highly enriched in light rare earth elements (LREE) and large ion lithophile elements (LILE; e.g., Rb, Ba, Sr), depleted in high field strength elements (HFSE; e.g., Nb, Ta, Ti), and show relatively homogeneous Sr-Nd isotopic compositions with initial 87Sr/86Sr = 0.70513-0.70597 and ɛNd(t) = - 5.8 to - 5.3. The data suggest that the Fanshan complex originated from a phlogopite-clinopyroxenite-rich lithosphere mantle source that had previously been metasomatized by melts from carbonated oceanic crust above a subduction zone. Highly radiogenic Os isotope compositions (initial 187Os/188Os = 0.299-2.449) suggest that the parent magma to the Fanshan complex has been contaminated by Precambrian mafic crustal rocks during magma emplacement in crustal levels. The occurrence of the Fanshan complex, together with many other ultramafic/alkaline plutons of similar ages, on the northern margin of the North China Craton suggests that the northern margin of the craton entered into a large-scale extensional regime in late Triassic after the final amalgamation between Mongolian microcontinent and the craton.

  16. Evolution of the geothermal fluids at Los Azufres, Mexico, as traced by noble gas isotopes, δ18O, δD, δ13C and 87Sr/86Sr

    Science.gov (United States)

    Pinti, D. L.; Castro, M. C.; Shouakar-Stash, O.; Tremblay, A.; Garduño, V. H.; Hall, C. M.; Hélie, J.-F.; Ghaleb, B.

    2013-01-01

    Isotopes of noble gases, CO2, H2O and Sr were measured in 10 geothermal wells and 8 hot springs, fumaroles and mud volcanoes at Los Azufres, the second most important geothermal field in Mexico. The aim of this study is to provide additional information on fluid circulation in the field and surrounding areas (Araró hot springs), as well as on physical processes such as boiling, steam separation and invasion of re-injected brines following over 25 years of geothermal fluid exploitation. Mantle helium dominates in fluids from the northern production zone of Marítaro, with measured 3He/4He ratios up to 7 Ra (where Ra is the atmospheric ratio of 1.386 × 10- 6). 3He/4He ratios are positively correlated with 87Sr/86Sr ratios and with δD and δ18O. These relationships suggest that Los Azufres fluids represent a mixing between primary magmatic 3He-rich fluids and groundwater currently discharging at Araró hot springs and enriched in radiogenic 4He acquired from Miocene andesites. Unusually high He ratios together with radiogenic Sr isotopic ratios suggest that thermal waters acquired mantle He from deep-seated parent magmas and radiogenic Sr possibly during their uprising through the metamorphic basement. 40Ar/36Ar ratios of 366 to 429 measured in two wells indicate either mantle-derived argon or a radiogenic 40Ar in situ component, suggesting the local presence of an older crustal fluid component in the northern part of the field. Ne, Kr and Xe are entirely of atmospheric origin, but processes of boiling, steam separation and re-injection of used brines have led to fractionation of their elemental abundances. Comparison with previous studies suggests that the boiling zone in the northern production zone is currently extending further north (Marítaro hot springs). In the southwestern productive zone, re-injected brines might account for more than 90% of the exploited fluids.

  17. Major element,trace element,and Sr,Nd and Pb iso-tope studies of Cenozoic basalts from the South China Sea

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The whole rock K-Ar ages of basalts from the South China Sea basin vary from 3.8 to 7.9 Ma, which suggest that intra-plate volcanism after the cessation of spreading of the South China Sea (SCS) is comparable to that in adjacent regions around the SCS, i.e., Leiqiong Peninsula, northern margin of the SCS, Indochina block, and so on. Based on detailed petrographic studies, we selected many fresh ba-saltic rocks and measured their major element, trace element, and Sr-Nd-Pb isotope compositions. Geochemical characteristics of major element and trace element show that these basaltic rocks belong to alkali basalt magma series, and are similar to OIB-type basalt. The extent of partial melting of mantle rock in source region is very low, and magma may experience crystallization differentiation and cu-mulation during the ascent to or storing in the high-level magma chamber. Sr-Nd-Pb isotopic data of these basaltic rocks imply an inhomogeneous mantle below the South China Sea. The nature of magma origin has a two end-member mixing model, one is EM2 (Enriched Mantle 2) which may be originated from mantle plume, the other is DMM (Depleted MORB Mantle). Pb isotopic characteristics show the Dupal anomaly in the South China Sea, and combined with newly found Dupal anomaly at Gakkel ridge in Arctic Ocean, this implies that Dupal anomaly is not only limited to South Hemisphere. In variation diagrams among Sr, Nd and Pb, the origin nature of mantle below the SCS is similar to those below Leiqiong peninsula, northern margin of the SCS and Indochina peninsula, and is different from those below north and northeast China. This study provides geochemical constraints on Hainan mantle plume.

  18. A petrologic, geochemical and Sr-Nd isotopic study on contact metamorphism and degassing of Devonian evaporites in the Norilsk aureoles, Siberia

    Science.gov (United States)

    Pang, Kwan-Nang; Arndt, Nicholas; Svensen, Henrik; Planke, Sverre; Polozov, Alexander; Polteau, Stephane; Iizuka, Yoshiyuki; Chung, Sun-Lin

    2013-04-01

    Devonian evaporites and associated sedimentary rocks in the Norilsk region were contact metamorphosed during emplacement of mafic sills that form part of the end-Permian (~252 Ma) Siberian Traps. We present mineralogical, geochemical and Sr-Nd isotopic data on sedimentary rocks unaffected by metamorphism, and meta-sedimentary rocks from selected contact aureoles at Norilsk, to examine the mechanisms responsible for magma-evaporite interaction and its relation to the end-Permian environmental crisis. The sedimentary rocks include massive anhydrite, rock salt, dolostone, calcareous siltstones and shale, and the meta-sedimentary rocks comprise calcareous hornfels, siliceous hornfels and minor meta-anhydrite and meta-sandstone. Contact metamorphism took place at low pressure and at maximum temperatures corresponding to the phlogopite-diopside stability field. Calcareous hornfels have high CaO, MgO, CΟ2, SΟ3, low SiO2 and initial Sr isotopic ratios of 0.7079-0.7092, features indicative of calcareous siltstone protoliths. Siliceous hornfels, in contrast, have high SiO2, Al2O3, Na2O, low in other major element oxides and initial Sr isotopic ratios of 0.7083-0.7152, consistent with pelitic or shaley protoliths. Loss of CO2 in a subset of calcareous hornfels can be explained by decarbonation reactions during metamorphism, but release of SO2 from evaporites cannot be accounted for by a similar mechanism. Occurrences of wollastonite and a variety of hydrous minerals in the calcareous hornfels are consistent with equilibration with hydrous fluid, which was capable of leaching large quantities of anhydrite in the presence of dissolved NaCl. In this way, substantial sediment-derived sulfur could have been mobilized, incorporated into the magmatic system and released to the atmosphere. The release of CO2 and SO2 from Siberian evaporites added to the variety of toxic gases generated during metamorphism of organic matter, coal and rock salt, contributing to the end

  19. Geochemical and Sr, Ca, U Isotopic Evidence of Recent changes of Weathering Reactions in a Forested Granitic Catchment (Strengbach Watershed, France)

    Science.gov (United States)

    Chabaux, F. J.; Pierret, M.; Stille, P.; Prunier, J.

    2009-12-01

    The characterization of the present-day weathering processes controlling the chemical composition of waters and soils and of their past evolution in natural ecosystems is important to predict and hence to model the response of the ecosystem to recent environmental changes. The geochemical analysis of the various hydro-geochemical compartments of experimental watersheds is well adapted to answer such questions. Here, we present the elemental and isotopic composition of soil solutions collected within two soil profiles located in the small granitic watershed of the Strengbach creek in the Vosges Mountain (France). The depth variation of elemental concentration confirms the important influence of the vegetation cycling on the budget of Ca, K, Rb and Sr, whereas Mg and Si budget in soil solutions are quasi exclusively controlled by weathering processes. Variation of Sr, Ca and U isotopic ratios with depth also demonstrates that the sources and biogeochemical processes controlling the Sr budget of soil solutions is different in the uppermost soil horizons and in the deeper ones. In the deeper part (>60cm) of the soil profile, dissolution of alumino-silicates is the main parameter accounting for the Sr budget of the soil solutions. The comparison of elemental concentrations and Sr isotope ratios in recent soil solutions with data obtained for soil solutions over the last 15 years, demonstrate that the source of elements in soil solutions has changed over this time period. Such a variation cannot be related to diminution of dissolution processes nor to declining of atmospheric input. It is related to a modification of the weathering reactions occurring within the weathering profile, including, most probably, an increasing dissolution of alumino-silicate minerals over 15 yrs. All our results demonstrate that the Strengbach watershed is in a transient state of weathering - with an important loss of nutriments such as Ca in soils solutions since at least 15yrs, associated

  20. Sr and U isotope ratios in soil waters as tracers of weathering dynamic in soils (Strengbach catchment - Vosges-mountains; France).

    Science.gov (United States)

    Chabaux, François; Prunier, Jonathan; Pierret, Marie-Claire; Stille, Peter

    2013-04-01

    It is proposed in this study to highlight the interest of multi-tracer geochemical approaches combining measurement of major and trace element concentrations along with U and Sr isotopic ratios to constrain the characterization of the present-day weathering processes controlling the chemical composition of waters and soils in natural ecosystems. This is important if we want to predict and to model correctly the response of ecosystems to recent environmental changes. The approach is applied to the small granitic Strengbah Catchment, located in the Vosges Mountain (France), used and equipped as a hydro-geochemical observatory since 1986 (Observatoire Hydro-Géochimique de l'Environnement; http://ohge.u-strasbg.fr). This study includes the analysis of major and trace element concentrations and (U-Sr) isotope ratios in soil solutions collected within two soil profiles located on two experimental plots of this watershed, along with the analysis of soil samples and vegetation samples from these two plots. The depth variation of elemental concentrations of soil solutions confirms the important influence of the vegetation cycling on the budget of Ca, K, Rb and Sr, whereas Mg and Si budget in soil solutions are quasi exclusively controlled by weathering processes. Variation of Sr, and U isotopic ratios with depth also demonstrates that the sources and biogeochemical processes controlling the Sr budget of soil solutions is different in the uppermost soil horizons and in the deeper ones, and clearly influence by the vegetation cycling. From the obtained data, it can be therefore proposed a scheme where in addition to the external flux associated to the decomposition of organic matter and throughfall, occurs a double lithogenic flux: a surface flux which can be associated to dissolution of secondary minerals contained in fine silt fractions and a deeper one, controlled by water-rock interactions which can mobilize elements from primary minerals like plagioclases or orthose

  1. Geochemistry, water dynamics and metals: Major, trace elements, Pb and Sr isotope constraints on their origins and movements in a small anthropized catchment over a flood

    Energy Technology Data Exchange (ETDEWEB)

    Luck, J.M.; Othman, D.B. [University Montpellier II, Laboratoire Geofluides, Bassins, Eaux, Montpellier (France)

    1997-10-01

    Major, trace elements and Sr-Pb isotope data on the dissolved and particulate phases are reported for water samples taken regularly over the September flood of a Mediterranean river (S France). This river drains runoff from a small, carbonate, karstified watershed with Miocene and Jurassic lithologies, and characterized by agricultural, urban and road network activities. The objective is to combine all the data into a dynamic model for constraining the origin(s) and movements of waters and of their loads. Furthermore, for metals, it becomes then feasible to know their fate and bioavailability downstream 18 refs., 4 figs.

  2. U-Pb Zircon geochronology and Sr-Nd isotopic characteristic of Late Neo proterozoic Born award granitoids (Taknar zone exotic block), Iran

    International Nuclear Information System (INIS)

    The study area (Born award granite) is located in northeast of Iran (Khorasan Razavi province), about 280 km southwest of Mashhad city. Taknar zone is an exotic block, bordered by two major faults, Great Kavir fault (Drouneh) to the south and Rivash fault in the north. A complex of granite, granodiorite, monzonite and diorite crop out at the center of Taknar zone. They are named as Bornaward granite. Published data using Rb-Sr whole-rock and biotite isotopic methods on granitoid rocks (Born award granite) gave ages of 154 to 111 Ma. The results of U-Pb zircon dating of granodiorite is 552.69 ± 10.89 Ma and granite is 538.22 - 1.82, + 4.28 Ma (Late Neo proterozoic time). Both granite and granodiorite are classified as belonging to the ilmenite-series of reduced S-type granitoids. Chemically, they are per-aluminous, high-K calc-alkaline with relatively enriched in LILE, Rb, K and depleted in Sr, Ba, Nb, Ti, Ta, Y and Yb. Chondrite-normalized Rare Earth Element plots indicate minor enrichments of light Rare Earth Element in composition with heavy Rare Earth Element, with (La/Yb)N between 3.5-5.6 and high total Rare Earth Element (193-252) with strong negative anomaly of Eu. They have a initial 87Sr/86Sr and 143Nd/144Nd ranging from 0.713566 to 0.716888 and 0.511791 to 0.511842, respectively, when recalculated to an age of 553 and 538 Ma, consistent with the new radiometric results. Initial εNd isotope values for granite and granodiorite range from -2,62 to -2,01. Granite and granodiorite of Born award yields a TDM age of 1.4-1.41 Ga. This indicates that the granites and granodiorite being derived from partial melting of distinct basement source regions with very high initial 87Sr/86Sr.

  3. Precise and accurate isotopic analysis of microscopic uranium-oxide grains using LA-MC-ICP-MS

    OpenAIRE

    Lloyd, Nicholas S.; Parrish, Randall R.; Horstwood, Matthew S.A.; Chenery, Simon R.N.

    2009-01-01

    Uranium isotope (235U, 236U, 238U) ratios were determined for microscopic uranium-oxide grains using laser-ablation multi-collector inductively-coupled-plasma mass-spectrometry (LA-MC-ICP-MS). The grains were retrieved from contaminated soil and dust samples. The analytical technique utilised is rapid, requires minimal sample preparation, and is well suited for nuclear forensic applications. Precision and accuracy were assessed by replicate analyses of natural uraninite grains: relative uncer...

  4. First measurement of Mg isotope abundances at high redshifts and accurate estimate of Delta alpha/alpha

    CERN Document Server

    Agafonova, I I; Levshakov, S A; Hou, J L

    2011-01-01

    (Abridged) We use a high-resolution spectrum of the quasar HE0001-2340 observed with the UVES/VLT to measure Mg isotope abundances in the intervening absorption-line systems at high redshifts. Line profiles are prepared accounting for possible shifts between the individual exposures. Due to unique composition of the selected systems - the presence of several transitions of the same ion - we can test the local accuracy of the wavelength scale calibration which is the main source of errors in the sub-pixel line position measurements. In the system at zabs = 0.45 which is probably a fragment of the outflow caused by SN Ia explosion of high-metallicity white dwarf(s) we measured velocity shifts of MgII and MgI lines relative to other lines (FeI, FeII, CaI, CaII): Delta V(MgII) = -0.44 +/- 0.05 km/s and Delta V(MgI) = -0.17 +/- 0.17$ km/s. This translates into the isotopic ratio 24Mg:25Mg:26Mg = (19 +/- 11):(22 +/- 13):(59 +/- 6) with a strong relative overabundance of heavy Mg isotopes, (25Mg+26Mg)/24Mg = 4, as c...

  5. Geochronology (U-Pb/Pb-Pb) and isotopic signatures (Rb-Sr/Sm-Nd) of the Paleoproterozoic Guanambi Batholith, southwest Bahia State (NE Brazil)

    International Nuclear Information System (INIS)

    The Guanambi batholith (GB) is located in south-western Bahia, Brazil, where it forms part of the Urandi-Paratinga mobile belt. The batholith extends over an area of almost 6,000 km2 and is mainly composed of syenites and monzonites, with subordinate granites, mafic syenites and lamprophyric dykes. Two main units can be recognized: the multiple intrusions, being divided into four regions (Paratinga, Laguna, Igapora and Guanambi) and the so-called late-intrusions forming the Cara Suja, Ceraima and Estreito massifs. U-Pb and Pb-Pb isotopic data demonstrate that the batholith was emplaced 2.05 Ga ago. GB has highly negative initial εNd (-7.4 to -10.6), pointing to an enriched source, and Sr initial ratios between 0.704 and 0.707. Both chemical and isotopic signatures suggest that GB formed by fractional crystallization of a lamprophiric magma derived from a Paleoproterozoic enriched mantle source. (author)

  6. Pb and Sr isotopes and trace metals in molluscs: constraints on metal sources and water fluxes in a coastal lagoon (Thau, France)

    International Nuclear Information System (INIS)

    Because of its unique ability to characterize the origins and quantify the fluxes of waters and their loads, isotopic geochemistry is being increasingly used in environmental problems. On the other hand, molluscs are known to concentrate metals in a very strong manner and equilibrate relatively rapidly with their environment. They are used in many programs of coastal survey (Mussel Watch, RNO,...). The originality of our work is to apply isotopic systems (Pb, Sr) to living organisms, in order to: 1- identify the metal sources; 2- determine their proportions in the lagoon and 3- to trace the water movements. The Thau lagoon (Herault, S. France) presents various potential sources of metals inputs: heavy traffic road, Sete harbour, various industries (cement factory, fertilizers...), agriculture, camping areas and leisure ports, not to mention natural (rock) sources. Our study deals with the metal and alkali, alkali-earth concentrations, Pb and Sr isotopes determined on both mussels implanted in the lagoon and wild mussels. We also compare our mussel results with those determined on clams which live at the water/sediments interface. A first study deals with the metal accumulation in laboratory experiments using mono-isotopic tracers 'spike'. It shows that the new metal is being superimposed to the metals initially present in the organisms; this effect is seen within a few days, although variable depending on elements (Zn, Cd, Pb). We have sampled the introduced mussels 4 times a year and we see that the concentration fluctuations are principally related to animal weight variations. The flesh isotopic compositions usually define nice alignments depending on season, indicative of a progressive mixing between two main components: one natural, one anthropogenic. Depending on winds,two influences of seawater entries or local water treatment plants effluents can be shown. We have compared past and present metal levels and origins in the area by analysing also ancient shells

  7. Sr-Nd-Pb isotope compositions of felsic intrusions in the El Teniente and Laguna La Huifa areas, Central Chile

    International Nuclear Information System (INIS)

    ) for being the main source of this type of magmatism. The presence of silicic lower crustal melts in the El Teniente region was earlier suggested by Kay and Kurtz (1995), who identified the geochemical fingerprint of mafic lower crust in postmineralization intrusives of the area. There is a growing regional scale, isotope data base that covers the timing of the magmatism at the El Teniente deposit (Kay and Kurtz, 1995; Stern and Skewes, 1995, Skewes and Stern, 1996 and Kurtz et al., 1997). Notwithstanding, there is still a need of additional data on a mine scale. The objective of this communication is to cover, at least partly, this need, presenting new Sr-Nd-Pb data. In the discussion section, we also discuss published Os isotope data from the El Teniente mine in order to further constrain the source of felsic magmatism linked to copper mineralization in the El Teniente and Laguna La Huifa areas (au)

  8. Contamination in mafic mineral-rich calc-alkaline granites: a geochemical and Sr-Nd isotope study of the Neoproterozoic Piedade Granite, SE Brazil

    Directory of Open Access Journals (Sweden)

    Leite Renato J.

    2006-01-01

    Full Text Available The Piedade Granite (~600 Ma was emplaced shortly after the main phase of granite magmatism in the Agudos Grandes batholith, Apiaí-Guaxupé Terrane, SE Brazil. Its main units are: mafic mineral-rich porphyritic granites forming the border (peraluminous muscovite-biotite granodiorite-monzogranite MBmg unit and core (metaluminous titanite-bearing biotite monzogranite BmgT unit and felsic pink inequigranular granite (Bmg unit between them. Bmg has high LaN/YbN (up to 100, Th/U (>10 and low Rb, Nb and Ta, and can be a crustal melt derived from deep-seated sources with residual garnet and biotite. The core BmgT unit derived from oxidized magmas with high Mg# (~45, Ba and Sr, fractionated REE patterns (LaN/YbN= 45, 87Sr/86Sr(t~ 0.710, epsilonNd(t ~ -12 to -14, interpreted as being high-K calc-alkaline magmas contaminated with metasedimentary rocks that had upper-crust signature (high U, Cs, Ta. The mafic-rich peraluminous granites show a more evolved isotope signature (87Sr/86Sr(t = 0.713-0.714; epsilonNd(t= -14 to -16, similar to Bmg, and Mg# and incompatible trace-element concentrations intermediate between Bmg and BmgT. A model is presented in whichMBmgis envisaged as the product of contamination between a mafic mineral-rich magma consanguineous with BmgT and pure crustal melts akin to Bmg.

  9. Origin of the deep fluids in the paleosubduction zones in western Tianshan: Evidence from Pb- and Sr-isotope compositions of high-pressure veins and host rocks

    Institute of Scientific and Technical Information of China (English)

    HUANG Dezhi; GAO Jun; DAI Tageng; ZOU Haiyang; XIONG Xianming; Reiner Klemd

    2005-01-01

    Fluids in the deep subduction zones play an important role in crust-mantle exchange related to the subduction process. Identification of fluids origin, internal or external, can help us to evaluate the contribution of crust materials to mantle during this process. High-pressure veins, which developed in the western Tianshan HP-metamorphic belt extensively, are the direct products of the fluids in subduction zones. In western Tianshan, high-pressure veins and host rocks have overall Pb- and Sr-isotope compositions. At t = 340 Ma, the high-pressure metamorphic time, the ratios of 206Pb/204Pb, 207Pb/204Pb, 208Pb/204Pb and 87Sr/86Sr of high pressure veins are 17.122―18.431, 15.477―15.611, 37.432―38.689 and 0.70529―0.70705, and are 17.605―17.834, 15.508―15.564, 37.080―38.145 and 0.70522―0.70685 for host rocks. However, high-pressure veins show a much larger variation in Pb-isotope compositions than host rocks. Plots of samples are distributed roughly along a line parallel to and far away from the Northern Hemisphere reference line (NHRL) on the plot of 206Pb/204Pb vs 207Pb/204Pb. On the plot of 206Pb/204Pb vs 208Pb/204Pb, plots of data are distributed nearby mid-ocean-ridge basalts (MORB) area or along a line parallel to and not far away from NHRL, which shows that the data plots are farther away from MORB and ocean island basalts (OIB) areas on the plot of 206Pb/204Pb vs 207Pb/204Pb than on the plot of 206Pb/204Pb vs 208Pb/204Pb. The compositions of Pb- and Sr-isotopes of these high-pressure metamorphic rocks are between that of enriched mantle 1(EMI) and of sediments or upper crust. A notable characteristic can be seen from plots of Pb-isotope ratio vs Pb-isotope ratio and 206Pb/204Pb vs 87Sr/86Sr that array of plots shows an evident tendency of mixture of two end members. Ratios of Rb/Ba, Ce/Pb, Nb/U and Ta/U of high-pressure veins and host rocks are between that of OIB or MORB and that of continental crust, which indicates that continental crust

  10. Accurate experimental determination of the isotope effects on the triple point temperature of water. II. Combined dependence on the 18O and 17O abundances

    Science.gov (United States)

    Faghihi, V.; Kozicki, M.; Aerts-Bijma, A. T.; Jansen, H. G.; Spriensma, J. J.; Peruzzi, A.; Meijer, H. A. J.

    2015-12-01

    This paper is the second of two articles on the quantification of isotope effects on the triple point temperature of water. In this second article, we address the combined effects of 18O and 17O isotopes. We manufactured five triple point cells with waters with 18O and 17O abundances exceeding widely the natural abundance range while maintaining their natural 18O/17O relationship. The 2H isotopic abundance was kept close to that of VSMOW (Vienna Standard Mean Ocean Water). These cells realized triple point temperatures ranging between  -220 μK to 1420 μK with respect to the temperature realized by a triple point cell filled with VSMOW. Our experiment allowed us to determine an accurate and reliable value for the newly defined combined 18, 17O correction parameter of AO  =  630 μK with a combined uncertainty of 10 μK. To apply this correction, only the 18O abundance of the TPW needs to be known (and the water needs to be of natural origin). Using the results of our two articles, we recommend a correction equation along with the coefficient values for isotopic compositions differing from that of VSMOW and compare the effect of this new equation on a number of triple point cells from the literature and from our own institute. Using our correction equation, the uncertainty in the isotope correction for triple point cell waters used around the world will be  <1 μK.

  11. Geochronology, geochemistry, and Sr-Nd-Hf isotopes of the early Paleozoic igneous rocks in the Duobaoshan area, NE China, and their geological significance

    Science.gov (United States)

    Wu, Guang; Chen, Yuchuan; Sun, Fengyue; Liu, Jun; Wang, Guorui; Xu, Bei

    2015-01-01

    The Duobaoshan area of northwestern Heilongjiang Province is the most important copper resource concentration region in NE China. To date, the Duobaoshan superlarge Cu-Mo deposit and the Tongshan large Cu-Mo deposit have been discovered in the Duobaoshan area. Both the deposits are hosted by granodiorites and volcanic rocks. Zircon LA-ICP-MS U-Pb dating indicates that these granodiorites emplaced approximately 479 Ma ago and that those volcanic rocks erupted between 447 and 450 Ma. The early Ordovicain granodiorites belong to the high-K to medium-K calc-alkaline series and are characterized by high Al2O3 and Sr contents, low Yb and Y contents, and relatively low Mg# values and Na2O/K2O ratios, with positive Eu or slight negative Eu anomalies (averaging 1.18). All of these geochemical characters are similar to those of the adakites generated by partial melting of a thickened lower crust in the world. Moreover, the granodiorites have low initial 87Sr/86Sr ratios (varying from 0.703474 to 0.704436), very high zircon εHf(t) and whole-rock εNd(t) values (varying from 13.0 to 16.8 and 5.27 to 5.46, respectively), and young zircon Hf and whole-rock Nd single-stage and two-stage model ages. Taking these geochemical characteristics and Sr-Nd-Hf isotope compositions together, we suggest that the early Ordovician granodiorites in the Duobaoshan area occurred in a post-collision environment and were formed by partial melting of a juvenile thickened lower crust dominated by depleted mantle-derived material. These late Ordovician volcanic rocks, which are composed of basalt, basaltic andesite, and andesite, belong to the tholeiitic or calc-alkaline series. They are generally enriched in large ion lithophile elements (LILEs) and depleted in high field strength elements (HFSEs; e.g., Nb, Ta, Zr, Hf, P, and Ti), consistent with the geochemistry of igneous rocks from island arcs or active continental margins. Compared with the early Ordovician granodiorites, these volcanic rocks

  12. Source contamination and mantle heterogeneity in the genesis of Italian potassic and ultrapotassic volcanic rocks: Sr-Nb-Pb isotope data from Roman Province and Southern Tuscany

    International Nuclear Information System (INIS)

    The Tyrrhenian border of the Italian peninsula has been the site of intense magmatism from Pliocene to recent times. Although calc-alkaline, potassic and ultrapotassic volcanism overlaps in space and time, a decrease of alkaline character in time and space (southward) is observed. Alkaline ultrapotassic and potassic volcanic rocks are characterized by variable enrichment in K and incompatible elements, coupled with consistently high LILE/IFSE values, similar to those of calc-alkaline volcanic rocks from the nearby Aeolian arc. On the basis of mineralogy and major and trace element chemistry two different arrays can be recognized among primitive rocks; a silica saturated trend, which resulted in formation of leucite-free mafic rocks, and a silica under saturated trend, characterized by leucite-bearing rocks. Initial 87Sr/87Sr and 143Nd/144Nd values of Italian ultrapotassic and potassic mafic rocks range from 0.70506 to 0.71672 and from 0.51173 to 0.51273, respectively. 207Pb/204Pb values range between 18.50 and 19.15, 207Pb/204Pb values range between 15.63 and 15.70, and 208Pb/204Pb values range between 38.35 and 39.20. The general εSr vs. εNd array, along with crustal lead isotopic values, clearly indicates that a continental crustal component has played an important role in the genesis of those magmas. The main question is where this continental crustal component has been acquired by the magmas. Volcanological and petrologic data indicate continental crustal contamination to be a leading process along with fractional crystallization and magma mixing. Considering, however, only the samples thought to represent primary magmas, which have been in equilibrium with their mantle source, a clearer picture emerges. A large variation of εSr vs. εNd is still observed, with εSr from -2 to +180 and εNd from +2 to -12. A bifurcation of this array is observed in the samples that plot in the lower right quadrant, with mafic leucite-bearing Roman Province rocks buffered at

  13. Sr-Nd-Pb isotope systematics and clinopyroxene-host disequilibrium in ultra-potassic magmas from Toro-Ankole and Virunga, East-African Rift: Implications for magma mixing and source heterogeneity

    Science.gov (United States)

    Muravyeva, N. S.; Belyatsky, B. V.; Senin, V. G.; Ivanov, A. V.

    2014-12-01

    Nd, Pb and Sr isotope ratios have been determined for kamafugite lava and clinopyroxene phenocrysts from Bunyaruguru (Toro-Ankole) and Virunga volcanic fields of the East African Rift. The whole rock Sr-Nd isotopic signatures of kamafugites (87Sr/86Sr: 0.70463-0.70536; 143Nd/144Nd: 0.51249-0.51255) suggest derivation from an EM1-type mantle source. In contrast, Pb isotopic compositions of the same samples (206Pb/204Pb: 19.00-19.57; 207Pb/204Pb: 15.69-15.74; 208Pb/204Pb: 39.30-40.26) reveal a similarity to EM2-type mantle. New Nd, Pb and Sr isotopic data for clinopyroxene (87Sr/86Sr: 0.70473-0.70503; 143Nd/144Nd: 0.51250-0.51254; 206Pb/204Pb: 18.04-18.17; 207Pb/204Pb: 15.58-15.60; 208Pb/204Pb: 38.09-38.23) suggest derivation from an EM1-like source, and indicate Sr and Pb isotope disequilibrium between clinopyroxene and corresponding host rock. Moreover, clinopyroxenes exhibiting a greater degree of isotopic disequilibrium with their host rock are more sodic in composition. The isotopic disequilibrium is corroborated by the presence of chemical zoning within clinopyroxene, which suggests rapid magma ascent rates preventing melt homogenization. The Pb isotopic ratios for both mineral and corresponding whole rock, together with published data on East African rift-related alkaline centers, define a trend interpreted to represent a mixing line for melts derived from sources such as EM1 and as HIMU. The similar isotopic compositions for clinopyroxene from the different volcanic rocks within the East African Rift suggest the existence of a common, older mantle source for their parental melts. The origin of these melts can be attributed to an enrichment event ~ 400-500 Ma, i.e., significantly prior the younger ultrapotassic magmatism. Our preferred interpretation for the results reported here involves the mixing of melts derived from EM1- and HIMU-like sources, which were rapidly transported to the Earth's surface. The primary magmas formed as the result of melting of a

  14. Geology, mineralization, U-Pb dating and Sr-Nd isotope geochemistry of intrusive bodies in northeast of Kashmar

    Directory of Open Access Journals (Sweden)

    Alireza Almasi

    2015-04-01

    Full Text Available Alireza Almasi1, Mohammad Hassan Karimpour1*, Khosrow Ebrahimi Nasrabadi1, Behnam Rahimi1, Urs KlÖtzli2 and Jose Francisco Santos3 Introduction The study area is located in central part of the Khaf- Kashmar-Bardeskan belt which is volcano-plutonic belt at the north of the Dorouneh fault in the north of Lut block. The north of the Lut block is affected by tectonic rotation and subduction processes which occur in the east of Iran (Tirrul et al., 1983. The magmatism of Lut block begins in Jurassic and continues in Tertiary (Aghanabati, 1995. Karimpour (Karimpour, 2006 pointed out the Khaf-Kashmar-Bardeskan belt has significant potential for IOCG type mineralization such as Kuh-e-Zar, Tannurjeh, and Sangan (Karimpour, 2006; Mazloumi, 2009. The data gathered on the I-type intrusive rocks include their field geology, petrography, U–Pb zircon dating and Sr–Nd isotope and also alteration and mineralization in the study area. Materials and methods - Preparation of 150 thin sections of rock samples for study of petrography and alteration of the intrusive rocks. - Magnetic susceptibility measuring of intrusive rocks. - U-Pb dating in zircon of I-type intrusive rocks by Laser-Ablation Multi Collector ICP-MS method. - Sr-Nd analysis on 5 samples of I-type intrusive rocks by Multi-Collector Thermal Ionization Mass Spectrometer (TIMS VG Sector 54 instrument. - Mineralography and paragenetic studies of ore-bearing quartz veins and geochemical analysis for 28 samples. - Production of the geology, alteration and mineralization maps by scale: 1:20000 in GIS. Results Oblique subduction in southern America initiated an arc-parallel fault and shear zones in the back of continental magmatic arc (Sillitoe, 2003. Because of this event, pull-apart basins were formed and high-K to shoshonitic calc-alkalineI- and A-type magmatism occur (Sillitoe, 2003. Most important deposits accompany with this magmatism are Au-Cu deposits types and Fe-Skarns (Sillitoe, 2003. We have

  15. U-Pb geochronology and Sr-Nd isotopes of Galileia and Urucum neo proterozoic granitoids suites in south-eastern Brazil

    International Nuclear Information System (INIS)

    U-Pb zircon and monazite dating and whole-rock Sr-Nd isotopes have been applied on Neo-Proterozoic granitoids from the Atlantic shear belt, south-eastern Brazil. U-Pb zircon results on the Galileia met-aluminous and Urucum per-aluminous suites indicate crystallisation ages of 594 ± 6 Ma and 582 ± 2 Ma respectively. Whole-rock Rb-Sr and Sm-Nd analyses on representative samples from both suites demonstrate that they mainly derive from melting of older crustal rocks. The occurrence of an old isotopic memory in the zircons from the Urucum granitoids around 2.2 Ga, in agreement with Nd model ages, suggests a Palaeo-Proterozoic age for the crustal proto-lith of these two suites, probably associated with the Transamazonico event. Owing to these new dating results and previous regional geochronological data, it can be proposed that the met-aluminous magmatism ended around 590 Ma and that the collisional peraluminous magmatism associated with the Brasiliano orogeny occurred between 584 and 570 Ma. (authors)

  16. Shoshonite and sub-alkaline magmas from an ultrapotassic volcano: Sr-Nd-Pb isotope data on the Roccamonfina volcanic rocks, Roman Magmatic Province, Southern Italy

    Science.gov (United States)

    Conticelli, Sandro; Marchionni, Sara; Rosa, Davide; Giordano, Guido; Boari, Elena; Avanzinelli, Riccardo

    2009-01-01

    The Roccamonfina volcano is characterised by two stages of volcanic activity that are separated by volcano-tectonic caldera collapses. Ultrapotassic leucite-bearing rocks are confined to the pre-caldera stage and display geochemical characteristics similar to those of other volcanoes in the Roman Province. After the major sector collapse of the volcano, occurred at ca. 400 ka, shoshonitic rocks erupted from cinder cones and domes both within the caldera and on the external flanks of the pre-caldera Roccamonfina volcano. On the basis of new trace element and Sr-Nd-Pb isotope data, we show that the Roccamonfina shoshonitic rocks are distinct from shoshonites of the Northern Roman Province, but are very similar to those of the Neapolitan volcanoes. The last phases of volcanic activity erupted sub-alkaline magmas as enclaves in trachytic domes, and as lavas within the Monte Santa Croce dome. Ultrapotassic rocks of the pre-caldera composite volcano are plagioclase-bearing leucitites characterised by high levels of incompatible trace elements with an orogenic signature having troughs at Ba, Ta, Nb, and Ti, and peaks at Cs, K, Th, U, and Pb. Initial values of 87Sr/86Sr range from 0.70926 to 0.70999, 143Nd/144Nd ranges from 0.51213 to 0.51217, while the lead isotope rations vary between 18.788-18.851 for 206Pb/204Pb, 15.685-15.701 for 207Pb/204Pb, and 39.048-39.076 for 208Pb/204Pb. Shoshonites show a similar pattern of trace element depletions and enrichments to the earlier ultrapotassic leucite-bearing rocks but have a larger degree of differentiation and lower concentrations of incompatible trace elements. On the other hand, shoshonitic rocks have Sr, Nd, and Pb isotopes consistently different than pre-caldera ultrapotassic leucite-bearing rocks. 87Sr/86Sr ranges from 0.70665 to 0.70745, 143Nd/144Nd ranges from 0.51234 to 0.51238, 206Pb/204Pb ranges from 18.924 to 19.153, 207Pb/204Pb ranges from 15.661 to 15.694, and 208Pb/204Pb ranges from 39.084 to 39.212. High-K calc

  17. Zircon U-Pb geochronology, geochemistry, and Sr-Nd-Hf isotopes of granitoids in the Yulekenhalasu copper ore district, northern Junggar, China: Petrogenesis and tectonic implications

    Science.gov (United States)

    Yang, Fuquan; Chai, Fengmei; Zhang, Zhixin; Geng, Xinxia; Li, Qiang

    2014-03-01

    The Yulekenhalasu porphyry copper deposit is located in the Kalaxiange'er metallogenic belt in northern Junggar, China. We present the results from zircon U-Pb geochronology, and geochemical and Sr-Nd-Hf isotope analyses of the granitoids associated with the ore deposits with a view to constrain their petrogenesis and tectonic setting. The granitoids consist of quartz diorite, diorite porphyry, porphyritic monzonite, and quartz porphyry, emplaced at 382, 379, 375-374, and 348 Ma, respectively, which span Late Devonian to early Carboniferous ages. The ore-bearing intrusion is mainly diorite porphyry, with subordinate porphyritic monzonite. The Late Devonian intrusions are characterized by SiO2 contents of 54.5-64.79 wt.%, Na2O contents of 3.82-8.24 wt.%, enrichment in Na, light rare-earth elements (LREEs), and large ion lithophile elements. They also display relative depletion in Y, Ba, P, Nb, Ta, and Ti, and weak negative Eu anomalies (δEu = 0.6-0.87). The early Carboniferous quartz porphyry is characterized by high SiO2 content (72.26-73.35 wt.%), enrichment in LREEs, K, and Sr, and relative depletion in Y (10.82-12.52 ppm) and Yb (1.06-1.15 ppm). The Late Devonian and early Carboniferous granitoids are characterized by positive ɛNd(t) values (5.2-10.1, one sample at - 1.9), positive ɛHf(t) values (7.46-18.45), low (87Sr/86Sr)i values (0.70363-0.70476), and young crustal residence ages. These data indicate that the sources of the granitoids were mainly mantle-derived juvenile rocks. Geochemical and Nd-Sr-Hf isotopic data demonstrate that the Late Devonian granitoids formed in an oceanic island arc, and they were formed from different sources, among which the mineralized diorite porphyry might have originated from a mixed slab-derived and mantle wedge melt source. The early Carboniferous quartz porphyry was likely emplaced in a mature island arc environment, and was probably derived from juvenile crust.

  18. The significance of PGE variations with Sr-Nd isotopes and lithophile elements in the Emeishan flood basalt province from SW China to northern Vietnam

    Science.gov (United States)

    Li, Chusi; Ripley, Edward M.; Tao, Yan; Hu, Ruizhong

    2016-04-01

    New analyses of siderophile-lithophile elements and Sr-Nd isotopes in the Permian basalts and picrites from northern Vietnam, the southernmost occurrence of the Emeishan flood basalt province, together with previously published data, are used to address the question of whether any meaningful correlation between these elements and isotopes exists at a province scale. The available data show that negative correlations between εNd, (87Sr/86Sr)i and mantle-normalized (Nb/Th)n are present in the basalts but not in the associated picrites. This indicates that crustal contamination is negligible in the picrites but significant in some of the basalts. The picrites and basalts from the entire province show negative correlations between (Rh/Ru)n, (Pt/Ru)n, (Pd/Ru)n and Mg-number. This indicates that Ru behaves compatibly whereas Rh, Pt and Pd behave incompatibly during magma differentiation. The incompatible behavior of Rh in natural basaltic systems is also supported by the fact that (Pt/Rh)n remains constant with decreasing Mg-number in the lavas. Depletions of Pd and Pt, and to a lesser degree Cu, in some basaltic samples characterized by relatively low εNd and (Nb/Th)n support the notion that sulfide saturation in the magmas was triggered by a combination of siliceous crustal contamination and addition of external sulfur. Within the entire flood basalt province only the picrites from Song Da, northern Vietnam show clear depletion in Ir relative to Ru. These picrites are also characterized higher Al2O3/TiO2 and lower mantle-normalized La/Yb (0.2-2.4) than those from elsewhere in the province, possibly due to the involvement of an Ir-depleted, fertile mantle component in magma generation at this location.

  19. Late Archaean mantle metasomatism below eastern Indian craton: Evidence from trace elements, REE geochemistry and Sr-Nd-O isotope systematics of ultramafic dykes

    Indian Academy of Sciences (India)

    Abhijit Roy; A Sarkar; S Jeyakumar; S K Aggrawal; M Ebihara; H Satoh

    2004-12-01

    Trace, rare earth elements (REE), Rb-Sr, Sm-Nd and O isotope studies have been carried out on ultramafic (harzburgite and lherzolite) dykes belonging to the newer dolerite dyke swarms of eastern Indian craton. The dyke swarms were earlier considered to be the youngest mafic magmatic activity in this region having ages not older than middle to late Proterozoic. The study indicates that the ultramafic members of these swarms are in fact of late Archaean age (Rb-Sr isochron age 2613 ± 177 Ma, Sri ∼0.702 ± 0.004) which attests that out of all the cratonic blocks of India, eastern Indian craton experienced earliest stabilization event. Primitive mantle normalized trace element plots of these dykes display enrichment in large ion lithophile elements (LILE), pronounced Ba, Nb and Sr depletions but very high concentrations of Cr and Ni. Chondrite normalised REE plots exhibit light REE (LREE) enrichment with nearly flat heavy REE (HREE; ( HREE)N ∼ 2-3 times chondrite, (Gd/Yb)N∼1). The Nd(t) values vary from +1.23 to −3.27 whereas 18O values vary from +3.16‰ to +5.29‰ (average +3.97‰ ± 0.75‰) which is lighter than the average mantle value. Isotopic, trace and REE data together indicate that during 2.6 Ga the nearly primitive mantle below the eastern Indian Craton was metasomatised by the fluid (±silicate melt) coming out from the subducting early crust resulting in LILE and LREE enriched, Nb depleted, variable Nd, low Sri(0.702) and low 18O bearing EMI type mantle. Magmatic blobs of this metasomatised mantle were subsequently emplaced in deeper levels of the granitic crust which possibly originated due to the same thermal pulse.

  20. Mantle influence on the character of I-type granitoids of the New England batholith: evidence from Sr and Nd isotopes

    International Nuclear Information System (INIS)

    Granitoid samples, together with an array of mafic to felsic dyke rocks, were collected from both the southern members of the high-K Moonbi Suite (Moonbi district) and the southern members of the low-K Clarence River Suite (Barrington Tops Granodiorite). These constitute the two most divergent compositions in the spectrum of I-type granitoids in the New England Batholith. Mafic plutonic rocks (quartz diorites) also coexist with granitoids at Barrington Tops (Eggins and Hensen 1987), and mafic dykes (high-K lamprophyres) have been observed in association with Moonbi Suite granitoids in the Hillgrove area (Kent 1994). Kent (1994) noted that lamprophyres in the Rockvale area extend the linear trends of the Moonbi granitoids on Harker plots, and the petrographic and chemical similarities between mafic and felsic intrusives at Barrington Tops have been described by Eggins and Hensen (1987). Shaw et al. (1992) also noted that lamprophyre dykes at Tulcumba Ridge (to the west of Tamworth) have similar ages and initial Sr isotopic compositions to Moonbi Suite granitoids (87Sr/86Sri 0.7042-0.7048). Lamprophyre dykes and felsic dykes of dacitic composition within the Moonbi Adamellite and the surrounding area were analysed for their Sr and Nd isotopic compositions, in an attempt to determine a link between mafic, mantle derived magmas and their granitoid hosts. Although isotopic and geochemical evidence provides a clear link between mantle-derived mafic magmas and granitoids within both the Moonbi and Clarence River suites, a clear explanation of the mechanisms and source rocks involved in magma generation remains elusive. Of critical importance is identification of the character of the lower crustal sources involved in each case, and clarification of the mechanism of interaction between the mantle and crustal sources. In particular, although the lamprophyres associated with the Moonbi Suite appear partly responsible for the isotopic and geochemical character (in particular

  1. A hybrid origin for two Cretaceous monzonitic plutons in eastern Zhejiang Province, Southeast China: Geochronological, geochemical, and Sr-Nd-Hf isotopic evidence

    Science.gov (United States)

    Liu, Liang; Qiu, Jian-Sheng; Zhao, Jiao-Long

    2016-01-01

    Monzonites can provide important information about the nature of the mantle sources and the mechanism of crust-mantle interactions. However, details on the origin of Late Mesozoic monzonites in the Southeastern China remain poorly constrained. This paper presents whole-rock geochemical, Sr-Nd isotopic and zircon U-Pb and Hf isotopic data for two monzonitic plutons (Huangtanyang and Kanggu) in eastern Zhejiang Province, with the aim of elucidating their petrogenesis, and providing important insights into the process of crust-mantle interaction. LA-ICP-MS zircon U-Pb dating results imply that the Huangtanyang and Kanggu quartz monzonites were emplaced in Cretaceous (104-109 Ma). All quartz monzonites are intermediate to acidic, metaluminous to weakly peraluminous, subalkaline, and K-rich in composition. They are enriched in large ion lithophile (e.g., Rb, Ba and Pb) and light rare earth elements, depleted in high-field strength elements (e.g., Nb, Ta, and Ti), and show weakly negative or no Eu anomalies (δEu = 0.78-1.02). All quartz monzonites have homogeneous initial ISr values (0.7084-0.7090) and εNd(t) values (-7.50 to -6.84). They are characterised by highly variable zircon Hf isotopic compositions, with εHf(t) values ranging from -13.3 to -5.7. The combined geochemical evidences (such as high Mg# values, low Nb/U and Ta/U ratios, and variable zircon Hf isotopic compositions) suggests that both depleted asthenospheric and metasomatically enriched mantle components were involved in the formation of the monzonites. The existence of some zircons with unusually low εHf(t) values (low to -13.3) and Palaeoproterozoic two-stage Hf model ages from the Huangtanyang and Kanggu quartz monzonites also argues strongly for Palaeoproterozoic crustal involvement. Magma mixing played a dominated role in the genesis of these monzonites, as indicated by their wide range in zircon Hf isotopic compositions and the occurrence of mafic microgranular enclaves (MMEs). The MMEs show

  2. Nd-Sr Isotopic Geochemistry of the Late Archean-Paleoproterozoic Granitoids in the Lüliang-Wutai Terrain, North China Craton,and Implications for Petrogenesis

    Institute of Scientific and Technical Information of China (English)

    CHEN Bin; LIU Shuwen; WANG Rui; CHEN Zhichao; LIU Chaoqun

    2006-01-01

    In this paper we report geochemical and Nd-Sr isotopic data for a late Archean gneissic granitic pluton (Hengling pluton), an early Paleoproterozoic complex (Xipan complex) and a late China, to trace the source of these late Archean-Paleoproterozoic granitoids and, particularly, to understand the nature and mechanism of continental growth at that time. The Hengling granitic gneisses (ca. 2.51 Ga) are characterized by high Na2O and LILEs, TTG-like REE patterns (highly depleted HREE and minor Eu anomalies) and moderately depleted Nd-Sr isotopic compositions (εNd(t)=1.2-2.7, ISr=0.7015-0.7019), and were considered as being products of arc magmatism that was developed upon the North China craton. The Xipan complex (ca. 2.2 Ga) contain gabbroic diorite and monzonite, mostly being Na2O-rich, highly fractionated REE patterns and isotopically enriched (εNd(t)=-1.5 to -4.1, ISr=0.7038-0.706). The gabbroic diorites probably originated from melting of an enriched mantle source, but significantly contaminated by lower crustal material, and the monzonites probably represent a product of a mixture between the gabbroic dioritic magma and granitic melts of crustal origin. The Yunzhongshan post-collisional granitoids (ca. 1.8 Ga) are characterized by high-K affinity and highly-enriched and homogeneous Nd isotopic compositions (εNd(t)=-4.9 to -5.7), although they split into two groups in terms of REE patterns: one group showing elevated HREE (and Sc, Y and Zr)with significant negative Eu anomalies and the other showing highly depleted HREE and, to a lesser extent, mid-REE with negligible Eu anomalies. These granites are genetically related to a process of extensional collapse of a thickened orogen. They formed through magma mixing between mantlederived basaltic magmas and crust-derived granitic melts, followed by significant fractionation of ferromagnesian phases (like hornblende and Cpx) and feldspar and accessory zircons. Some Yunzhongshan granites show very old Nd model ages

  3. Beta-decay properties of neutron-rich Ge, Se, Kr, Sr, Ru, and Pd isotopes from deformed quasiparticle random-phase approximation

    CERN Document Server

    Sarriguren, P

    2015-01-01

    Beta-decay properties of even and odd-A neutron-rich Ge, Se, Kr, Sr, Ru, and Pd isotopes involved in the astrophysical rapid neutron capture process are studied within a deformed proton-neutron quasiparticle random-phase approximation. The underlying mean field is described self-consistently from deformed Skyrme Hartree-Fock calculations with pairing correlations. Residual interactions in the particle-hole and particle-particle channels are also included in the formalism. The isotopic evolution of the various nuclear equilibrium shapes and the corresponding charge radii are investigated in all the isotopic chains. The energy distributions of the Gamow-Teller strength as well as the beta-decay half-lives are discussed and compared with the available experimental information. It is shown that nuclear deformation plays a significant role in the description of the decay properties in this mass region. Reliable predictions of the strength distributions are essential to evaluate decay rates in astrophysical scenari...

  4. Rb-Sr and Sm-Nd isotopic studies of the Upper Paleozoic ignimbrites from Tokrau depression (Central Kazakhstan)

    International Nuclear Information System (INIS)

    Allowing for errors , Rb-Sr isochronous age of the Akron's massif ignimbrites (303±5 million years) and that of Korgants massif ones supper imposing them (299±5 million years) should be dated by 310±3 million years. The initial ratios (87Sr/86Sr), constitute 0.7046-0.7048 in the rocks of both massifs. And is positive and makes up 0.94-2.92. The crust's age, i. e. the source of ignimbrites forming molten runs up to 0.8-1.0 billion years by Nd-model dating. Within boundary of Middle Late Carboniferous there was no Pre-Raphanin granite continental crust below the Tokrau depression. (author)

  5. The role of magma mixing in the evolution of high-K calc-alkaline granitoid suites: in situ trace element and Sr-Nd-Hf isotope constraints

    Science.gov (United States)

    Laurent, Oscar; Zeh, Armin; Gerdes, Axel; Slaby, Ewa; Villaros, Arnaud

    2015-04-01

    The so-called "I-type", high-K calc-alkaline granitoids are often considered as "hybrid" in origin, i.e. involving both mantle and crustal components in their petrogenesis. The interactions between both components either take place (1) at mantle levels (i.e. enriched mantle source); (2) at emplacement levels (i.e. crustal contamination and/or magma mixing with crustal melts) or (3) both. Magma mixing is, in particular, frequently invoked to explain the compositional range of high-K calc-alkaline granitoid suites, especially phases of intermediate composition (SiO2 = 60-65 wt.%) such as quartz-diorites or granodiorites. We investigated the role of magma mixing in the origin of such rocks using elemental and isotope (Sr-Nd-Hf) chemistry of magmatic minerals (plagioclase, zircon, apatite, titanite, epidote), measured in situ by LA-(MC-)ICPMS, allowing a much greater spatial resolution than classical whole-rock geochemistry. We focused on a suite of late-Archaean (2.69 Ga-old) high-K, calc-alkaline granitoids from the Pietersburg block, northern Kaapvaal Craton (South Africa): the Mashashane, Matlala, Matok and Moletsi plutons. Those plutons range from diorites to monzogranites, emplaced at different crustal levels but all within a relatively short time span and showing evidence for interactions (mingling), both at the outcrop and mineral scale. Hf isotope data on zircon confirm that all rocks are cogenetic (identical ɛHf(t)), but trace element and Sr isotopes in plagioclase point to the involvement of several components in their petrogenesis, at different stages of the magma evolution. The most mafic rocks (diorites) derive from the interaction, at mantle levels, between depleted peridotite and a sedimentary component of quartzofeldspathic nature. The mineral chemistry of more felsic rocks can be explained by (1) differentiation from the diorite magmas through Amp + Plag fractionation; (2) interactions with magmas derived from melting of local crust (tonalites

  6. Mixing and melt sources in the Miocene Aztec Wash pluton (Nevada, USA) as revealed by zircon Hf and O and whole rock Sr, Nd, and Hf isotopes

    Science.gov (United States)

    Ryan, M.; Miller, J. S.; Miller, C. F.; Bromley, S.; Davies, G. R.; Schmitt, A. K.

    2011-12-01

    The 15.6 Ma Aztec Wash Pluton (AWP) is one of several Miocene intrusions located within the northern Colorado River extensional corridor. Extensive E-W tilting of fault blocks has exposed the pluton from the roof to 5 km structural depth. Earlier field and petrologic studies subdivided the AWP into two distinct zones: (1) a Granite Zone (GZ) comprised of relatively homogeneous granite with subtle differences in textures and mineralogy; (2) a Heterogeneous Zone (HZ), which interfingers the GZ, contains evidence for mafic and felsic magma input with a wide compositional range (42-78 wt% SiO2), and abundant field evidence for hybridization. Previous whole rock geochemistry and zircon trace element analyses indicated that compositional variation was produced by multi-component mixing between mafic and felsic melts within the HZ. New whole rock Sr, Nd, and Hf isotope data from the HZ show that all rocks (including high-silica granites) formed by mixing Precambrian crust and enriched mantle, with mixtures having a large mantle fraction (≥50%). New Hf (n=189) and O (n=241) isotope analyses of zircon from samples in the HZ confirm these melt sources and provide a broader perspective on hybridization processes within the AWP. Zircon grains from all samples show heterogeneous Hf and O isotopic compositions (-5 to -18 ɛHf; 4.5-7.5% δ18O), but despite the clear signature of Precambrian crust in the whole rock data, obvious Precambrian zircons (or cores) were mostly absent; only one zircon was clearly Precambrian (ɛHf = -25). Resolvable intragrain variability is relatively limited (including the Precambrian grain, which is unzoned). Zircons from hand samples and from compositional groups also show heterogeneous ɛHf and δ18O values, although the spreads are more restricted than in the whole data set (6-10 ɛHf in granites, 5-7 ɛHf in intermediate "hybrids", 5-6 ɛHf in gabbro/diorite sheets). Oxygen isotope values for the zircons also show intra-handsample heterogeneity

  7. Study of recent changes of weathering dynamic in soils based on Sr and U isotope ratios in soil solutions (Strengbach catchment- Vosges, France)

    Science.gov (United States)

    Prunier, Jonathan; Chabaux, François; Stille, Peter; Pierret, Marie-Claire; Viville, Daniel; Gangloff, Sophie

    2015-04-01

    Major and trace element concentrations along with U and Sr isotopic ratios of the main components of the water-soil-plant system of two experimental plots in a forested silicate catchment were determined to characterize the day-present weathering processes within the surface soil levels and to identify the nature of minerals which control the lithogenic flux of the soil solutions. This study allows recognition of a lithogenic origin of the dissolved U in the surface soil solutions, even in the most superficial ones, implying that the colloidal U is a U secondarily associated with organic matter or organo-metallic complexes. This flux significantly varies in the upper meter of the soil and between the two sites, due to their slightly different bedrock lithologies and likely also to their different vegetation covers. A long-time monitoring during the past 15 years was achieved to evaluate the response of this ecosystem to recent environmental changes. A clear decrease of the Ca and K fluxes exported by the soil solutions between 1992 and 2006 at the spruce site was observed, while this decrease is much smaller for the beech plot. In addition, the Sr isotope ratios of soil solutions vary significantly between 1998 and 2004, with once again a much more important change for the spruce site than for the beech site. It demonstrates that the source of elements in soil solutions has changed over this time period due to a modification of the weathering reactions occurring within the weathering profile. The origin of the weathering modification could be the consequence of the acid rains on weathering granitic bedrock or a consequence of forest exploitation incompatible with the nutriment reserve of soils with recent plantations of conifer, which impoverish soils. All together, these data suggest that the forest ecosystem at the spruce plot is in a transient state of functioning marked by a possible recent modification of weathering reactions. This study shows the potential of

  8. Rb-Sr isotopic composition of granites in the Western Krušné hory/Erzgebirge pluton, Central Europe: record of variations in source lithologies, mafic magma input and postmagmatic hydrothermal events

    Science.gov (United States)

    Dolejš, David; Bendl, Jiří; Štemprok, Miroslav

    2016-10-01

    The late Variscan (327-318 Ma) Western Krušné hory/Erzgebirge pluton (Czech Republic and Germany) represents a multiply emplaced intrusive sequence ranging from low-F biotite monzogranites (with rare minor bodies of gabbrodiorites and granodiorites) to high-F topaz-zinnwaldite alkali-feldspar granites. This granite suite is characterized by progressively increasing concentrations of incompatible elements (Li, Rb, F), monotonous decrease in mafic components and compatible elements (FeOtot, MgO, TiO2, CaO, Sr) with increasing silica. Consequently, this leads to extreme variations in the Rb/Sr ratios (0.52 to 59), which impose highly variable 87Rb/86Sr and 87Sr/86Sr signatures. The low-F biotite monzogranites represent isotopically heterogeneous mixture with (87Sr/86Sr)323 = 0.707-0.709 between partial melts from the Saxothuringian metasediments and mantle-derived mafic precursors. The medium-F two-mica microgranites show variable (87Sr/86Sr)323 = 0.708-0.714, indicating involvement of multiple precursors and more mature crustal protoliths. The evolved high-F topaz-zinnwaldite alkali-feldspar granites were derived from a precursor with (87Sr/86Sr)320 = 0.707-0.708 at 324-317 Ma by differentiation, which produced the extreme Rb/Sr enrichment and variations. The Li/Rb ratios remain nearly constant (~0.5), thus insensitive to the degree of geochemical differentiation. In comparison to terrestrial variations, the high Li/Rb values indicate derivation of granitic magmas from predominantly sedimentary precursors, in accord with 7Li-6Li and 143Nd-144Nd isotope composition reported previously. The Rb-Sr element variations in each granite unit are sligthly different and indicate ascent and emplacement of separate magma batches, which do not form a single liquid line of descent. We consider the enrichment of granites in incompatible elements (Li, Rb, F) and compatible depletion of ferromagnesian components, CaO and Sr as a combined effect of multiple precursors, changes in

  9. Geothermal waters from the Taupo Volcanic Zone; New Zealand: a view through Li, B and Sr isotopes

    OpenAIRE

    Millot, Romain; Hegan, Aimee; Négrel, Philippe

    2011-01-01

    International audience In the present work, we report chemical and isotope data for 23 geothermal water samples from the Taupo Volcanic Zone (TVZ) in New Zealand. The Taupo Volcanic Zone has anomalously high heat flow and widespread hydrothermal activity. Chemical and isotope data were analyzed for these deep geothermal waters in order to provide further constraints on the characterization of the associated deep geothermal reservoirs. The present study aims therefore to characterize the fl...

  10. Isotopic characteristics (Nd and Sr) of the intrusive plutonism at the northwestern Amazonian Craton, Venezuela, and implications for the Paleoproterozoic evolution

    International Nuclear Information System (INIS)

    Nd and Sr analyses were performed on selected granitoid plutons that intrude Archean and Paleoproterozoic domains of the Guyana shield (Venezuela). The isotopic signatures of these plutons together with the geochronologic background of the country rocks are used to constrain their magma genesis and tectonic setting within the Paleoproterozoic evolutions of mobile belts (Maroni-Itacaiunas and Ventuari-Tapajos provinces) of the Amazonian Craton. The Encrucijada Suite (2187 +- 94 Ma), which intrudes Archean rocks of the Imataca Complex, originated predominantly from partial melt of this crust, as supported by negative epsilonNd(2.1Ga) values (-2.2 to - 4.9) and TDM ages between 2.82 and 2.49 Ga. Conversely, the plutons from the Supamo Complex (2230 - 2050 Ma) and Cuchivero Group (1980 - 1830 Ma), occurring within the adjoining Paleoproterozoic provinces, are juvenile in nature (derived from roughly contemporary protoliths). These bodies display TDM ages between 2.13 and 2.22 Ga, as well as positive epsilonNd(2.1Ga) values (+0.74 to + 3.05). Isotopic correlation diagrams 143 Nd/144 Nd vs. 147 Sm/144 Nd and 143 Nd/144 Nd vs. time) plotted together with the plutonic rocks and Imataca Complex rocks were evaluated taking into account the geologic background of the NW part of the Amazonian Craton. Interpretation of these isotopic data supports the idea of tectonic juxtaposition between the Imataca Complex and the Maroni-Itacaiunas province during the Transamazonian orogeny (2.25 - 2.05 Ga). On the other hand, the Cuchivero Group plutons have a contrasting isotopic signature compared to the other Paleoproterozoic plutonic rocks. This is consistent with the existence of a tectonic boundary between the Maroni-Itacaiunas and the Ventuari-Tapajos province in the late Paleoproterozoic. (author)

  11. Isotopic Ratio Outlier Analysis of the S. cerevisiae Metabolome Using Accurate Mass Gas Chromatography/Time-of-Flight Mass Spectrometry: A New Method for Discovery.

    Science.gov (United States)

    Qiu, Yunping; Moir, Robyn; Willis, Ian; Beecher, Chris; Tsai, Yu-Hsuan; Garrett, Timothy J; Yost, Richard A; Kurland, Irwin J

    2016-03-01

    Isotopic ratio outlier analysis (IROA) is a (13)C metabolomics profiling method that eliminates sample to sample variance, discriminates against noise and artifacts, and improves identification of compounds, previously done with accurate mass liquid chromatography/mass spectrometry (LC/MS). This is the first report using IROA technology in combination with accurate mass gas chromatography/time-of-flight mass spectrometry (GC/TOF-MS), here used to examine the S. cerevisiae metabolome. S. cerevisiae was grown in YNB media, containing randomized 95% (13)C, or 5%(13)C glucose as the single carbon source, in order that the isotopomer pattern of all metabolites would mirror the labeled glucose. When these IROA experiments are combined, the abundance of the heavy isotopologues in the 5%(13)C extracts, or light isotopologues in the 95%(13)C extracts, follows the binomial distribution, showing mirrored peak pairs for the molecular ion. The mass difference between the (12)C monoisotopic and the (13)C monoisotopic equals the number of carbons in the molecules. The IROA-GC/MS protocol developed, using both chemical and electron ionization, extends the information acquired from the isotopic peak patterns for formulas generation. The process that can be formulated as an algorithm, in which the number of carbons, as well as the number of methoximations and silylations are used as search constraints. In electron impact (EI/IROA) spectra, the artifactual peaks are identified and easily removed, which has the potential to generate "clean" EI libraries. The combination of chemical ionization (CI) IROA and EI/IROA affords a metabolite identification procedure that enables the identification of coeluting metabolites, and allowed us to characterize 126 metabolites in the current study. PMID:26820234

  12. A Sr-Nd isotopic study of sand-sized sediment provenance and transport for the San Francisco Bay coastal system

    Science.gov (United States)

    Rosenbauer, Robert J.; Foxgrover, Amy C.; Hein, James R.; Swarzenski, Peter W.

    2013-01-01

    A diverse suite of geochemical tracers, including 87Sr/86Sr and 143Nd/144Nd isotope ratios, the rare earth elements (REEs), and select trace elements were used to determine sand-sized sediment provenance and transport pathways within the San Francisco Bay coastal system. This study complements a large interdisciplinary effort (Barnard et al., 2012) that seeks to better understand recent geomorphic change in a highly urbanized and dynamic estuarine-coastal setting. Sand-sized sediment provenance in this geologically complex system is important to estuarine resource managers and was assessed by examining the geographic distribution of this suite of geochemical tracers from the primary sources (fluvial and rock) throughout the bay, adjacent coast, and beaches. Due to their intrinsic geochemical nature, 143Nd/144Nd isotopic ratios provide the most resolved picture of where sediment in this system is likely sourced and how it moves through this estuarine system into the Pacific Ocean. For example, Nd isotopes confirm that the predominant source of sand-sized sediment to Suisun Bay, San Pablo Bay, and Central Bay is the Sierra Nevada Batholith via the Sacramento River, with lesser contributions from the Napa and San Joaquin Rivers. Isotopic ratios also reveal hot-spots of local sediment accumulation, such as the basalt and chert deposits around the Golden Gate Bridge and the high magnetite deposits of Ocean Beach. Sand-sized sediment that exits San Francisco Bay accumulates on the ebb-tidal delta and is in part conveyed southward by long-shore currents. Broadly, the geochemical tracers reveal a complex story of multiple sediment sources, dynamic intra-bay sediment mixing and reworking, and eventual dilution and transport by energetic marine processes. Combined geochemical results provide information on sediment movement into and through San Francisco Bay and further our understanding of how sustained anthropogenic activities which limit sediment inputs to the system (e

  13. Important role of magma mixing in generating the Mesozoic monzodioritic-granodioritic intrusions related to Cu mineralization, Tongling, East China: Evidence from petrological and in situ Sr-Hf isotopic data

    Science.gov (United States)

    Chen, C. J.; Chen, B.; Li, Z.; Wang, Z. Q.

    2016-04-01

    The Mesozoic ore-bearing high-Mg monzodioritic-granodioritic rocks in the Tongling mining district (East China) have been described as having adakitic affinities, and their origin has been attributed to partial melting of delaminated eclogite at depth in the mantle, followed by interaction of the resultant granitic magma with mantle peridotite. Here we present petrological data and in situ Sr isotopic data for zoned plagioclase that are inconsistent with the eclogite-derived model and instead propose a model that involves magma mixing of siliceous crustal melts and basaltic magma that was derived from metasomatized mantle in a back-arc extensional regime. The principal geochemical signatures of these Mesozoic rocks include a high-K calc-alkaline affinity, high values of Mg#, high Sr-Ba abundances, high Sr/Y and La/Yb ratios, εNd(t) = - 13.1 to - 9.0, and ISr = 0.70707-0.70824. The magma mixing model is supported by (1) the common existence of mafic microgranular enclaves (MMEs) and the disequilibrium textures of plagioclase and amphibole, (2) the 87Sr/86Sr ratios of embayed high-Ca cores of plagioclase that are distinctly lower than in the euhedral low-Ca overgrowth rims, (3) the negative correlations between whole-rock Nd and Sr isotopic ratios, and (4) the significant differences in the values of εHf(t) (- 9.5 to - 26) within different zircons from the same intrusion.

  14. Petrogenesis of Granitoids, U-Pb zircon geochronology, Sr-Nd Petrogenesis of granitoids, U-Pb zircon geochronology, Sr-Nd isotopic characteristics, and important occurrence of Tertiary mineralization within the Lut block, eastern Iran

    Directory of Open Access Journals (Sweden)

    M.H. Karimpour

    2012-04-01

    Full Text Available Tertiary intrusive granitoids within the Lut block in the Khorasan Razavi and South Khorasan provinces are mainly sub-volcanic with porphyry texture and their composition varies from granite to diorite but monzonite is dominant. With the exception of Hired, these are classified as belonging to the magnetite-series of I-type granitoids. Chemically, these rocks are meta-aluminous. Those with mineralization are K-rich and those without mineralization such as Najmabad are Na-rich. All intrusive rocks plot in the field of calc-alkaline to adakite except Najmabad that plot in the adakite field. Based on low content of Nb (30, low initial 87Sr/86Sr (17 ppm, low ratio of Zr/Nb (0.707 and low initial εNd value (-3, magmas in the Kaybar-Kuh were more contaminated in the continental crust. Based on depletion in HREE and high ratio of (La/YbN (17-23, magma in Najmabad originated in the deep region in which garnet was present. Based on REE pattern and ration of Eu/Eu* (0.8-1, intrusive rocks within Maherabad, Khoopik, Chah-Shaljami, Kuh Shah and Dehsalm are calc-alkaline and their magma formed in an oxidant condition whereas Kaybar Kuh magma with low ratio of Eu/Eu* (<0.8 was contaminated in the continental crust under reduced conditions. The age of these granitoids is between Middle Eocene and Lower Oligocene. Kaybar-Kuh (43.3 Ma is situated in the north and Chah-Shaljami (33.3 Ma in the south. The initial 87Sr/86Sr ratios decrease from north (0.7077 to south (0.7047 as the age decreases. εNd of Maherabad, Khoopik, Dehsalm, and Chah-Shaljami granitoids is between +0.5 and +2.49 and the initial 87Sr/86Sr ratio is less than 0.7055. The age of the source rock (TDM, which was calculated based on Sm-Nd isotopes indicates that these magma originated from oceanic crust with different ages. Kaybar-Kuh originated from the oldest oceanic crust (840 Ma and was contaminated more in continental crust, but Najmabad originated from a younger oceanic crust (360 Ma with

  15. Chemical and isotopic ( 87Sr/ 86Sr, δ 18O, δD) constraints to the formation processes of Red-Sea brines

    Science.gov (United States)

    Pierret, M. C.; Clauer, N.; Bosch, D.; Blanc, G.; France-Lanord, C.

    2001-04-01

    About twenty deeps filled with hot brines and/or metalliferous sediments, are located along the Red-Sea axis. These brines present a well-suited framework to study the hydrothermal activity in such a young ocean. The present study outlines the results of a geochemical approach combining major-, trace-element and isotopic (oxygen, hydrogen, strontium) analyses of brines in six of the deeps, to evaluate different processes of brine formation and to compare the evolution of each deep. Important heterogeneities in temperature, salinity, hydrographic structure and chemistry are recorded, each brine having its own characteristics. The intensity of hydrothermal circulation varies among the deeps and ranges from being strong (Atlantis II and Nereus) to weak (Port-Soudan) and even to negligible (Valdivia and Suakin) and it varies along the entire Red-Sea axis. These observations do not favour a unique formational model for all of the brines. For example, the brines of the Suakin deep appear to have been formed by an old sea water which dissolved evaporite beds, without significant fluid circulation and hydrothermal input, while others such as Atlantis II or Nereus Deeps appear to be dominated by hydrothermal influences. A striking feature is the absence of a relationship between the position of the deeps along the axis and their evolutionary maturity.

  16. Non-depleted sub-continental mantle beneath the Superior Province of the Canadian Shield: Nd-Sr isotopic and trace element evidence from Midcontinent Rift basalts

    Energy Technology Data Exchange (ETDEWEB)

    Paces, J.B. (Michigan Technological Univ., Houghton (USA)); Bell, K. (Carleton Univ., Ottawa, Ontario (Canada))

    1989-08-01

    Midcontinent Rift flood basalts represent a sample of the relatively shallow, sub-continental upper mantle beneath the Canadian Shield at 1.1 Ga. A thick sequence of olivine tholeiite lavas, including minor intermediate to rhyolitic lavas, from the Portage Lake Volcanics (PLV) in northern Michigan have initial Nd and Sr isotopic compositions which cluster near Bulk Earth values. The effects of assimilation of old LREE-enriched continental crust into mantle-derived fractionating liquids are isotopically discernible in evolved lavas as well as in olivine tholeiites from the lowest portion of the volcanic pile. However, the effects of crustal contamination decrease with stratigraphic height and are absent in more primitive lavas in the upper half of the section. The source for PLV tholeiites is substantially less depleted than previously reported mantle values from the Superior Province. An origin for the PLV source is compatible with either of several mantle evolution models. The PLV source may have been associated with upwelling of a LIL element-enriched, asthenospheric plume which emplaced non-depleted material from deeper sources into the shallow sub-continental mantle beneath the Midcontinent Rift during continental break-up. Alternatively, the PLV source may have originated by enrichment of refractory sub-continental lithospheric mantle which was previously depleted in incompatible trace elements during Archean-aged melt extraction and continental crust formation. Concurrent generation of carbonatite magmas in other areas beneath the Superior Province indicates the widespread presence of sub-continental mantle with substantially higher {epsilon}{sub Nd}(T) and lower {epsilon}{sub Sr}(T) than the PLV source.

  17. Genesis of granitoid batholiths of Peninsular Malaysia and implications for models of crustal evolution: Evidence from a NdSr isotopic and UPb zircon study

    Science.gov (United States)

    Liew, T. C.; McCulloch, M. T.

    1985-02-01

    Nd, Sr and U-Pb isotopic data for the late Triassic West Coast Province batholiths and Permian to Triassic East Coast Province batholiths of Peninsular Malaysia allow estimates of the ages of the crustal fragments comprising the peninsula to be made. Initial ɛNd and ɛSr values for granitoids from the West Coast Province range from -6 to -10 and +160(0.716) to +660(0.751) respectively. Nd model ages calculated based on a depleted mantle evolution model ( TDMNd) range from 1300 Ma to 1800 Ma and are in general agreement with the mid-Proterozoic upper intersection ages of U-Pb zircon reverse discordia (1500-1700 Ma). Initial ɛNd and ɛSr values for granitoids from the East Coast Province range from -0.8 to -6 and +10(0.705) to +130(0.714) respectively. Calculated TDMNd ages of 900-1400 Ma for these granitoids are comparable to two U-Pb zircon reverse discordia intercepts that yield 800 Ma and 1350 Ma. The general agreement of U-Pb zircon inheritance ages and TDMNd ages are interpreted to correspond to the Proterozoic 'crust formation' ages of the continental fragments represented by the West Coast and East Coast batholithic provinces. Mid-Proterozoic (~ 1300-1900 Ma) 'crust formation' ages are commonly shown by other Phanerozoic continental margin plutonic and volcanic belts. The ubiquitous mid-Proterozoic 'crust formation' ages and the absence of Archaean signatures suggest voluminous juvenile additions to the continental crust in the mid-Proterozoic. Such ages at continental margins would imply that many continental blocks had achieved very much their present-day extent by the mid-Proterozoic.

  18. Zircon U-Pb age, geochemical, and Sr-Nd-Pb isotopic constraints on the origin of alkaline intrusions in eastern Shandong Province, China

    Science.gov (United States)

    Liu, Shen; Feng, Caixia; Hu, Ruizhong; Gao, Shan; Wang, Tao; Feng, Guangying; Qi, Youqiang; Coulson, Ian M.; Lai, Shaocong

    2013-08-01

    Alkaline intrusions in the eastern Shandong Province consist of quartz monzonite and granite. U-Pb zircon ages, geochemical data, and Sr-Nd-Pb isotopic data for these rocks are reported in the present paper. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) U-Pb zircon analyses yielded consistent ages ranging from 114.3 ± 0.3 to 122.3 ± 0.4 Ma for six samples of the felsic rocks. The felsic rocks are characterised by a wide range of chemical compositions (SiO2 = 55.14-77.63 wt. %, MgO = 0.09-4.64 wt. %, Fe2O3 = 0.56-7.6 wt. %, CaO = 0.40-5.2 wt. %), light rare earth elements (LREEs) and large ion lithophile elements (LILEs) (i.e., Rb, Pb, U) enrichment, as well as significant rare earth elements (HREEs) and heavy field strength (HFSEs) (Nb, Ta, P and Ti) depletion, various and high (87Sr/86Sr) i ranging from 0.7066 to 0.7087, low ɛ Nd (t) values from -14.1 to -17.1, high neodymium model ages (TDM1 = 1.56-2.38Ga, TDM2 = 2.02-2.25Ga), 206Pb/204Pb = 17.12-17.16, 207Pb/204Pb = 15.44-15.51, and 208Pb/204Pb = 37.55-37.72. The results suggested that these rocks were derived from an enriched crustal source. In addition, the alkaline rocks also evolved as the result of the fractionation of potassium feldspar, plagioclase, +/- ilmenite or rutile and apatite. However, the alkaline rocks were not affected by crustal contamination. Moreover, the generation of the alkaline rocks can be attributed to the structural collapse of the Sulu organic belt due to various processes.

  19. Rb-Sr and Sm-Nd isotopic and REE studies of igneous components in the bulk matrix domain of Martian breccia Northwest Africa 7034

    Science.gov (United States)

    Nyquist, Laurence E.; Shih, Chi-Yu; McCubbin, Francis M.; Santos, Alison R.; Shearer, Charles K.; Peng, Zhan X.; Burger, Paul V.; Agee, Carl B.

    2016-03-01

    The bulk matrix domain of the Martian breccia NWA 7034 was examined petrographically and isotopically to better understand the provenance and age of the source material that make up the breccia. Both 147Sm-143Nd and 146Sm-142Nd age results for mineral separates from the bulk matrix portion of breccia NWA 7034 suggest that various lithological components in the breccia probably formed contemporaneously ~4.44 Ga ago. This old age is in excellent agreement with the upper intersection ages (4.35-4.45 Ga) for U-Pb discordia and also concordia defined by zircon and baddeleyite grains in matrix and igneous-textured clasts. Consequently, we confirm an ancient age for the igneous components that make up the NWA 7034 breccia. Substantial disturbance in the Rb-Sr system was detected, and no age significance could be gleaned from our Rb-Sr data. The disturbance to the Rb-Sr system may be due to a thermal event recorded by bulk-rock K-Ar ages of 1.56 Ga and U-Pb ages of phosphates at about 1.35-1.5 Ga, which suggest partial resetting from an unknown thermal event(s), possibly accompanying breccia formation. The NWA 7034 bulk rock is LREE enriched and similar to KREEP-rich lunar rocks, which indicates that the earliest Martian crust was geochemically enriched. This enrichment supports the idea that the crust is one of the enriched geochemical reservoirs on Mars that have been detected in studies of other Martian meteorites.

  20. Source area and seasonal Sr-87/Sr-86 variations in rivers of the Amazon basin

    OpenAIRE

    R. V. Santos; Sondag, Francis; Cochonneau, Gérard; Lagane, C.; Brunet, P.; Hattingh, K.; Chaves, J. G. S.

    2015-01-01

    We report the results of a detailed study of dissolved Sr isotopes in the Solimoes and Beni-Madeira Rivers of the Amazon basin. This study developed data collected over 8years indicating large spatial and temporal variations in dissolved Sr isotopes among the rivers of the Amazon basin. The large Sr-87/Sr-86 variations were found to be correlated with the geology of the source areas of the suspended sediments. The Beni-Madeira River displays a high average Sr-87/Sr-86 ratio and large Sr-87/Sr...

  1. Hybrid genesis of Jurassic fayalite-bearing felsic subvolcanic rocks in South China: Inspired by petrography, geochronology, and Sr-Nd-O-Hf isotopes

    Science.gov (United States)

    Guo, Chunli; Zeng, Lingsen; Li, Qiuli; Fu, Jianming; Ding, Tiping

    2016-11-01

    Fayalite-bearing felsic (FBF) magmatic rocks are a special type of granitic rocks with controversial origins. A suite of fayalite- and ferrosilite-bearing subvolcanic rocks, namely, the Xishan FBF rocks in South China, is investigated in this study. The Xishan FBF rocks have high SiO2 contents of 69-70 wt.%, high K2O/Na2O ratios of 1.71-1.95, and high FeOt/(FeOt + MgO) ratios of 0.88-0.89. Fayalite (Fo = 7.3-9.6) and ferrosilite (Fs = 74.1-76.5) minerals are found in the Xishan FBF rocks. According to the Unmix function of Isoplot, the zircon U-Pb ages and initial Hf isotope compositions are categorized into two groups with ages of 156.6 Ma and 151.5 Ma and εHf(t) values of - 7.1 and - 5.2, respectively. The minerals show δ18O values of 8.8-9.8‰ for zircon, 6.0-8.1‰ for fayalite, and 7.0-8.2‰ for ferrosilite. The oxygen isotope fractionations between ferrosilite and fayalite (ΔOpx-Ol) vary from - 0.8‰ to + 1.5‰, which indicates disequilibrium crystallization. Whole-rock analyses show high initial 87Sr/86Sr ratios of 0.7169 to 0.7180 and negative εNd(t) values of - 7.3 to - 6.8; zircon analyses show εHf(t) values of - 9.1 to - 3.8 and δ18O values of 8.8-9.8‰. So whole rock and zircon isotopes indicate a crustal signature. Based on these mineralogical and geochemical data, the Xishan FBF rocks were attributed to A-type granites and derived from the mixing of two batches of crustal magmas, which were all derived from the partial melting of ancient igneous protolith under the conditions of high temperature (683-893 °C), moderate water (3-5 wt.%), and low oxygen fugacity (lg fO2 = - 1.21). Such rigorous physical conditions may be common for the FBF igneous rocks all over the world, which may be the primary factors controlling occurrence of the FBF rocks in limited volume and quantity.

  2. Geochemistry of major and trace elements and Pb–Sr isotopes of a weathering profile developed on the Lower Cambrian black shales in central Hunan, China

    International Nuclear Information System (INIS)

    Highlights: • The chemical changes during black shale weathering are geochemically estimated. • Chemical changes and Pb–Sr data suggest four types of chemical reactions. • There were two stages of geochemical processes during black shale weathering. • Early stage of chemical differentiation led elements leaching and redistribution. • Soil was formed by later chemical homogenisation after the early differentiation. - Abstract: This paper reports a geochemical study on the major and trace elements and Pb–Sr isotopes of a weathering profile developed in the Lower Cambrian black shales in central Hunan (China). Six weathering horizons were identified and sampled vertically throughout the profile. The chemical composition of the profile consists of variable concentrations of the major elements Fe2O3, FeO, MnO, MgO, CaO, Na2O, and P2O5 and of less variable concentrations of SiO2, TiO2, Al2O3, and K2O. The chemical change caused by weathering is estimated by mass-balance calculations, and the results show that the element mobility is characterised by substantial loss of SiO2, FeO, CaO, K2O, Na2O, LOI, Cr, V, Ba, Cs, Rb, Sr, U, and Th, and moderate loss of Al2O3, MgO, Fe2O3, Ni, Cu, Pb, Tl, Sn, Sc, Ge and REE (Y). The high field strength elements TiO2, Sn, Sc, U, Ga, Ge, Zr, Hf, Nb, and Ta were immobile during weathering. The chemical changes and the Pb–Sr isotopic data suggest that four types of chemical reactions occurred: the oxidation of sulphide minerals (e.g., pyrite) and organic carbon (OS), the dissolution of less resistant clinochlore-Ia, calcite, and P-bearing minerals (DL), the dissolution of detrital albite and microcline (DA), and the transformation of clay (TC) minerals (e.g., muscovite and illite–smectite). These chemical reactions then led to two stages of geochemical processes, an early stage of chemical differentiation and a later stage of chemical homogenisation. The chemical differentiation dominated by the OS, DL, and DA reactions

  3. Repumping and spectroscopy of laser-cooled Sr atoms using the (5s5p)3P2-(5s4d)3D2 transition

    Science.gov (United States)

    Mickelson, P. G.; Martinez de Escobar, Y. N.; Anzel, P.; De Salvo, B. J.; Nagel, S. B.; Traverso, A. J.; Yan, M.; Killian, T. C.

    2009-12-01

    We describe repumping and spectroscopy of laser-cooled strontium (Sr) atoms using the (5s5p)3P2-(5s4d)3D2 transition. Atom number in a magneto-optical trap is enhanced by driving this transition because Sr atoms that have decayed into the (5s5p)3P2 dark state are repumped back into the (5s2)1S0 ground state. Spectroscopy of 84Sr, 86Sr, 87Sr and 88Sr improves the value of the (5s5p)3P2-(5s4d)3D2 transition frequency and determines the isotope shifts for the transition accurately enough to guide laser-cooling experiments with less abundant isotopes.

  4. Paleoproterozoic crustal evolution in the East Sarmatian Orogen: Petrology, geochemistry, Sr-Nd isotopes and zircon U-Pb geochronology of andesites from the Voronezh massif, Western Russia

    Science.gov (United States)

    Terentiev, R. A.; Savko, K. A.; Santosh, M.

    2016-03-01

    Andesites and related plutonic rocks are major contributors to continental growth and provide insights into the interaction between the mantle and crust. Paleoproterozoic volcanic rocks are important components of the East Sarmatian Orogen (ESO) belonging to the East European Craton, although their petrogenesis and tectonic setting remain controversial. Here we present petrology, mineral chemistry, bulk chemistry, Sr-Nd isotopes, and zircon U-Pb geochronological data from andesites and related rocks in the Losevo and Vorontsovka blocks of the ESO. Clinopyroxene phenocrysts in the andesites are depleted in LREE, and enriched in HFSE (Th, Nb, Zr, Hf, Ti) and LILE (Ba, Sr). Based on the chemistry of pyroxenes and whole rocks, as well as Fe-Ti oxides, we estimate a temperature range of 1179 to 1262 °C, pressures of 11.3 to 13.0 kbar, H2O content of 1-5 wt.%, and oxygen fu gacity close to the MH buffer for the melts of the Kalach graben (KG) and the Baygora area (BA) andesites. Our zircon U-Pb geochronological data indicate new zircon growth during the middle Paleoproterozoic as displayed by weighted mean 207Pb/206Pb ages of 2047 ± 17 Ma and 2040 ± 16 Ma for andesite and dacite-porphyry of the BA, and 2050 ± 16 Ma from high-Mg basaltic andesite of the KG. The andesites and related rocks of the KG and BA are characterized by high magnesium contents (Mg # up to 0.68). All these volcanic rocks are depleted in LREE and HFSE, and display negative Nb and Ti anomalies relative to primitive mantle. The high-Mg bulk composition, and the presence of clinopyroxene phenocrysts suggests that the parent melts of the KG and BA suite were in equilibrium with the mantle rocks. The rocks show positive εNd(T) values and low initial 87Sr/86Sr, suggesting that the magmas were mostly derived from metasomatized mantle source. The geochemical differences between the two andesite types are attributed to: the predominance of fractional crystallization, and minor role of contamination in the

  5. Nd, Sr and Pb isotopic composition of metasomatised xenoliths from the backarc Patagonian Mantle Wedge: Insights into the origin of the uprising melts

    Science.gov (United States)

    Zanetti, Alberto; Mazzucchelli, Maurizio; Hemond, Christope; Cipriani, Anna; Bertotto, Gustavo W.; Cingolani, Carlos; Vannucci, Riccardo

    2010-05-01

    Information about the geochemical composition of metasomatic melts migrating through the Patagonian mantle wedge is provided by the ultramafic xenoliths occurrence of Tres Lagos (TL; lat. 49.13°S, long. 71.18°W), Argentina. Such a locality is placed at the eastern border of the Meseta de la Muerte backarc basaltic plateau, where a post-plateau volcanic diatreme contains mantle xenoliths in both pyroclastites and lavas. Its latitude corresponds with the Northern limit of the Austral Volcanic Arc (AVZ), which is separated from the Southern Volcanic Zone (SVZ) by a gap in the arc magmatism ranging between 49° and 46°30' latitude S. The analysed xenoliths have been distinguished into two groups (Group 1 & 2). Group 1 consists of lherzolites and harzburgites, whereas Group 2 is formed by harzburgites. The texture of the Group 1 lherzolites varies from protogranular to granoblastic to porphyroblastic, whereas Group 1 harzburgites have always granoblastic texture. Group 2 harzburgites have granular texture, which may change to porphyroblastic owing to the random concentration of large olivine and orthopyroxene crystals. The clinopyroxenes (Cpx) from Group 1 lherzolites have PM-normalised REE patterns ranging from LREE-depleted (LaN/SmN= 0.24-0.37), to LREE-enriched (LaN/YbN up to 4.08) and spoon-shaped: the latter have minimum at Pr and Pr-Yb concentrations similar to those shown by the LREE-depleted Cpx. The Cpx from Group 1 harzburgites have lower REE concentrations with respect to the lherzolite ones and their REE patterns vary from HREE-enriched, steadily fractionated, (LaN/YbN = 0.21-0.35, Ybn ~ 1-2) to spoon-shaped (LaN/SmN = 2.81; SmN/YbN = 0.89; YbN ~ 3. The Cpx from the Group 2 harzburgites have convex-upward (LaN/SmN = 0.31; SmN/YbN = 1.50) to LREE-enriched (LaN/YbN = 2.94) patterns. The Sr, Nd and Pb isotopic compositions of the Group 1 clinopyroxenes form arrays spanning from DM to the field delimited by the TL basaltic lavas, pointing to EMI end

  6. Mantle and crustal processes in the magmatism of the Campania region: inferences from mineralogy, geochemistry, and Sr-Nd-O isotopes of young hybrid volcanics of the Ischia island (South Italy)

    Science.gov (United States)

    D'Antonio, Massimo; Tonarini, Sonia; Arienzo, Ilenia; Civetta, Lucia; Dallai, Luigi; Moretti, Roberto; Orsi, Giovanni; Andria, Mariachiara; Trecalli, Alberto

    2013-06-01

    Ischia, one active volcano of the Phlegraean Volcanic District, prone to very high risk, is dominated by a caldera formed 55 ka BP, followed by resurgence of the collapsed area. Over the past 3 ka, the activity extruded evolved potassic magmas; only a few low-energy explosive events were fed by less evolved magmas. A geochemical and Sr-Nd-O isotope investigation has been performed on minerals and glass from products of three of such eruptions, Molara, Vateliero, and Cava Nocelle (Ischia volcanism in the past. Detailed study on the most mafic magma has permitted to investigate its origin. The mantle sector below Ischia underwent subduction processes that modified its pristine chemical, isotopic, and redox conditions by addition of ≤1 % of sediment fluids/melts. Similar processes occurred from Southeast to Northwest along the Apennine compressive margin, with addition of up to 2.5 % of sediment-derived material. This is shown by volcanics with poorly variable, typical δ18O mantle values, and 87Sr/86Sr progressively increasing toward typical continental crust values. Multiple partial melting of this modified mantle generated distinct primary magmas that occasionally assimilated continental crust, acquiring more 18O than 87Sr. At Ischia, 7 % of Hercynian granodiorite assimilation produced isotopically distinct, K-basaltic to latitic magmas. A SW-NE regional tectonic structure gave these magmas coming from large depth the opportunity to mingle/mix with felsic magmas stagnating in shallower reservoirs, eventually triggering explosive eruptions.

  7. Rb-Sr whole-rock and mineral ages, K-Ar, 40Ar/39Ar, and U-Pb mineral ages, and strontium, lead, neodymium, and oxygen isotopic compositions for granitic rocks from the Salinian Composite Terrane, California:

    Science.gov (United States)

    Kistler, R.W.; Champion, D.E.

    2001-01-01

    This report summarizes new and published age and isotopic data for whole-rocks and minerals from granitic rocks in the Salinian composite terrane, California. Rubidium-strontium whole-rock ages of plutons are in two groups, Early Cretaceous (122 to 100 Ma) and Late Cretaceous (95 to 82 Ma). Early Cretaceous plutons occur in all granitic rock exposures from Bodega Head in the north to those from the Santa Lucia and Gabilan Ranges in the central part of the terrane. Late Cretaceous plutons have been identified in the Point Reyes Peninsula, the Santa Lucia and the Gabilan Ranges, and in the La Panza Range in the southern part of the terrane. Ranges of initial values of isotopic compositions are 87Sr/86Sr, 0.7046-0.7147, δ18O, +8.5 to +12.5 per mil, 206Pb/204Pb, 18.901-19.860, 207Pb/204Pb, 15.618-15.814, 208Pb/204Pb, 38.569- 39.493, and εNd, +0.9 to -8.6. The initial 87Sr/86Sr=0.706 isopleth is identified in the northern Gabilan Range and in the Ben Lomond area of the Santa Cruz Mountains, in Montara Mountain, in Bodega Head, and to the west of the Farallon Islands on the Cordell Bank. This isotopic boundary is offset about 95 miles (160km) by right-lateral displacements along the San Gregorio-Hosgri and San Andreas fault systems.

  8. Sr, C and O isotopes as markers of alkaline disturbances in the Toarcian argillites of the Tournemire experimental platform (France). Case of a 15-years old engineered analogue.

    Science.gov (United States)

    Techer, I.; Boulvais, P.; Bartier, D.; Tinseau, E.

    2009-04-01

    argillites close to the cement-concrete contact. These data are detailed in another session of this meeting (Techer et al., ERE6 session). In order to precise the spatial extent of the disturbances and to discuss the nature of the responsible fluids, a systematic chemical and isotopic study was performed focusing on the Sr, C and O isotopes known to be very good markers of alkaline fluids percolation (Fourcade et al. 2006). Four studied levels were selected according to their location on the DM overcore and the nature of the cementitious material in contact to the argillites: -155 cm level (DM155) and -180 cm level (DM180) where argillites were in contact with a 1.5 to 3 cm thick concrete; -245 cm level (DM245) and -300 cm level (DM300) where the cementitious material was represented by a fine grained Portland cement 2 to 5 cm thick. Samples of the cementitious materials were collected at each level. Argillites were sampled perpendicularly to the cement-concrete contact with a continuous sampling every 2 to 5 mm millimeters (P1). Micro-fissures developed perpendicularly to the cement-concrete contact were opened and infilling secondary minerals were collected by scrap as a function of the distance to the cement-concrete (P3). Along P1 and P3, no significant variation of the carbonates d18O isotopic values was observed in the argillites. On the opposite d13C and 87Sr/86Sr values of these minerals changed significantly in the direct contact with the cement-concrete over a distance of 15 to 25 mm. Beyond this distance, argillites were again well bedded and showed values similar to those measured in a reference sample. Negative d13C values measured in the disturbed zone and close to those encountered in the cement and the concrete argued for a perturbation induced by an alkaline solution. 87Sr/86Sr isotopic ratios showed a progressive evolution in the disturbed zone, with increasing trends towards the cementitious material. Thanks to complementary Sr elementary contents

  9. REE and Sr-Nd isotope characteristics of hydrothermal chimney at Jade area in the Okinawa Trough

    Institute of Scientific and Technical Information of China (English)

    LIU Yanguang; MENG Xianwei; FU Yunxia

    2004-01-01

    Hydrothermal chimney is a product of hydrothermal activity on the seabed. Chimney samples dredged from Jade hydrothermal area in Izena depression of the Okinawa Trough, are characterized by relatively enriched light rare earth elements (LREE) and strongly positive Eu anomalies. 87Sr/86Sr and 143Nd/144Nd of these samples are exactly between those of seawater and of acidic pumice, averaged at 0.708928 and 0.512292, respectively. These characteristics imply that the main source of hydrothermal sulfide at Jade area is possibly the undersurface acidic rocks. The mineralizing mechanism can be summarized as follows: Large amount of mineralized material would be leached out and LREEenriched hydrothermal solution would be subsequently produced as a result of thermo-chemical exchange reaction between acidic volcanic rocks and heated seawater that penetrated in advance from upper water mass. The spurting out from the seabed and quickly crystallizing in the seawater of hydrothermal solution are responsible for the formation of Cu-Zn sulfide and barite-amorphous SiO2 minerals that are characterized by enriched LREE and positively strong Eu anomalies.

  10. Crustal evolution of granitoids and gneisses from the Cambaizinho belt, southern Brazil: Review zircon Pb-Pb evaporation ages and Pb-Nd-Sr isotopes

    International Nuclear Information System (INIS)

    Deformed granitoids and gneisses from the Cambai Complex (900-700 Ma) along Cambaizinho Creek and in the Vila Nova do Sul region, state of Rio Grande do Sul, Brazil, were formed in a remarkably short time, about 10 m.y., between 704±13 and 697±3 Ma. The data base of this work includes eighteen zircon Pb/Pb evaporation analyses, five Pb isotope in feldspar and whole rock. The oldest known rocks in the region are polydeformed dioritic gneisses dated by conventional U-Pb zircon at 704±13 Ma. New Pb-Pb zircon evaporation data on the late transcurrent, less deformed and more evolved granitoids (Sanga do Jobim Granitoids) yield a 697± Ma age and indicates that the evolution of the plutonic magmatism in the area was nearly contemporaneous. These data contrast with previous interpretations based on Rb-Sr data which considered that these rock associations were formed during a longer time period (700-640 Ma). All these granitoids intruded the supracrustal sequence. These granitoids yield a minimum age of about 700 Ma for the formation of the supracrustal sequence and its regional dynamothermal metamorphism. Lead isotope composition of K-feldspar from Sanga do Jobim Granitoids plot close to, but slightly below the lead isotope evolution curve of orogeny in the Zartmann and Doe model (1981). This indicates that the setting for these granitoids was that of a juvenile magmatic arc. These new data plus previous data in the region also corroborate that the crustal evolution involved juvenile crust accreted between 760-700 Ma. In contrast, the Cacapava and Sao Sepe Granites intruded the supracrustal sequences along the eastern side of the Sao Gabriel Block at 562 Ma and 550 Ma, respectively, and show Pb and Nd isotope signatures from an old basement. This evidence suggests that the juvenile terrane was thrusted over the older basement situated along the eastern part of the shield during the Dom Feliciano collisional orogeny at about 620-590 Ma (au)

  11. Geochemical and Sr-Nd-Pb-O isotope composition of granitoids of the Early Cretaceous Copiapó plutonic complex (27°30'S), Chile

    Science.gov (United States)

    Marschik, Robert; Fontignie, Denis; Chiaradia, Massimo; Voldet, Pia

    2003-10-01

    Early Cretaceous plutonic rocks exposed south of Copiapó form part of the Coastal Batholith of northern Chile. These rocks intrude arc-derived volcanic and volcaniclastic rocks and marine limestones that were deposited in the Early Cretaceous Atacama backarc basin. The Copiapó plutonic complex consists mainly of calc-alkaline, medium- to coarse-grained diorite, granodiorite, tonalite, monzodiorite, and quartz monzonite. The plutonic rocks are subalkaline to alkaline, metaluminous, magnetite-series, volcanic arc, I-type granitoids. Batholithic magmas are a heat, potential fluid, metal, and sulphur source for the hydrothermal iron oxide-rich Cu-Au mineralization in the Candelaria-Punta del Cobre district. Ore-related hydrothermal alteration affected large portions of the Copiapó complex. The least altered batholithic rocks have initial 87Sr/ 86Sr of 0.703070-0.703231; initial 143Nd/ 144Nd of 0.512733-0.512781; and 206Pb/ 204Pb, 207Pb/ 204Pb, and 208Pb/ 204Pb of 18.428-18.772, 15.550-15.603, and 38.127-38.401, respectively. The δ18O values for these rocks range from +6.9 to +8.6‰. Isotope signatures and trace element distributions suggest that the magmas are mantle derived. A subduction fluid-modified mantle source may explain the geochemical characteristics of the Copiapó complex. The ascent of magmas occurred along deep-rooted structures without significant crustal contamination, though minor contamination by relatively young (e.g. Jurassic) igneous rocks during ascent is possible. Intrusive rocks with high-K to shoshonitic characteristics probably represent residual liquids of less evolved magmas. The regional geologic context suggests that the plutons of the Copiapó complex were emplaced at a relatively shallow crustal level of 2-3 km.

  12. Mg/Ca, Sr/Ca, and stable isotopes in modern and Holocene Protothaca staminea shells from a northern California coastal upwelling region

    Science.gov (United States)

    Takesue, R.K.; VanGeen, A.

    2004-01-01

    This study explores the potential of intertidal Protothaca staminea shells as high-resolution geochemical archives of environmental change in a coastal upwelling region. Mg/Ca and Sr/Ca ratios were analyzed by excimer laser ablation-inductively coupled plasma mass spectrometry (LA-ICP-MS) at sub-weekly temporal resolution in shells growing ???1 mm per month. Growth patterns of a modern P. staminea shell from Humboldt Bay, California, collected in December 1999 made it possible to infer a lifespan from 1993 to 1998. Growth hiatuses in the shell may have excluded records of extreme events. Mg/Ca ratios appeared to be partly controlled by water temperature; the correlation coefficient between temperature and Mg/Ca was r = 0.71 in one of four growth increments. Significant year-to-year differences in the sensitivity of Mg/Ca to temperature in P. staminea could not be explained, however. Sr/Ca ratios appeared to be more closely related to shell growth rate. Oxygen isotopes, measured at 2-week temporal resolution in the same shell, did not show a clear relation to local temperature in summer, possibly because temperatures were higher and less variable at the King Salmon mudflat, where the shell was collected, than in the main channel of Humboldt Bay, where water properties were monitored. Negative shell ??13C values (upwelling events. The Mg contents of P. staminea midden shells dated to ???3 ka and ???9 ka were significantly lower than in the modern shell. This may have resulted from degradation of a Mg-rich shell organic matrix and precluded quantitative interpretation of the older high-resolution records. Elevated ??13C values in the ???3 ka shell suggested that the individual grew in highly productive or stratified environment, such as a shallow coastal embayment or lagoon. Copyright ?? 2004 Elsevier Ltd.

  13. Geochemical and Sr-Pb-Nd isotopic characteristics of the Shakhtama porphyry Mo-Cu system (Eastern Transbaikalia, Russia)

    Science.gov (United States)

    Berzina, A. P.; Berzina, A. N.; Gimon, V. O.

    2014-01-01

    The Shakhtama Mo-Cu porphyry deposit is located within the eastern segment of the Central Asian Orogenic Belt, bordering the southern margin of the Mongol-Okhotsk suture zone. The deposit includes rocks of two magmatic complexes: the precursor plutonic (J2) and ore-bearing porphyry (J3) complexes. The plutonic complex was emplaced at the final stages of the collisional regime in the region; the formation of the porphyry complex may have overlapped with a transition to extension. The Shakhtama rocks are predominantly metaluminous, I-type high K calc-alkaline to shoshonitic in composition, with relatively high Mg#, Ni, Cr and V. They are characterized by crustal-like ISr (0.70741-0.70782), relatively radiogenic Pb isotopic compositions, ɛNd(T) values close to CHUR (-2.7 to +2.1) and Nd model ages from 0.8 to 1.2 Ga. Both complexes are composed of rocks with K-adakitic features and rocks without adakite trace element signatures. The regional geological setting together with geochemical and isotopic data indicate that both juvenile and old continental crust contributed to their origin. High-Mg# K-adakitic Shakhtama magmas were most likely generated by partial melting of thickened lower crust during delamination and interaction with mantle material, while magmas lacking adakite-like signatures were probably generated at shallower levels of lower crust. The derivation of melts, related to the formation of plutonic and porphyry complexes involved variable amounts of old Precambrian lower crust and juvenile Phanerozoic crust. Isotopic data imply stronger contribution of juvenile mantle-derived material to the fertile magmas of the porphyry complex. Juvenile crust is proposed as an important source of fluids and metals for the Shakhtama ore-magmatic system.

  14. Geological, geochronological, geochemical, and Sr-Nd-O-Hf isotopic constraints on origins of intrusions associated with the Baishan porphyry Mo deposit in eastern Tianshan, NW China

    Science.gov (United States)

    Wang, Yinhong; Xue, Chunji; Liu, Jiajun; Zhang, Fangfang

    2016-10-01

    The Baishan porphyry Mo deposit (0.72 Mt; 0.06 % Mo) is located in the interior of the eastern Tianshan orogenic belt in Xinjiang, NW China. The deposit comprises 15 orebodies that are associated with monzogranite and granite porphyry stocks and are structurally controlled by roughly EW-trending faults. Secondary ion mass spectrometry (SIMS) zircon U-Pb dating of the monzogranite and granite porphyry yielded the Middle Triassic age (228 ± 2 to 227 ± 2 Ma), which coincide with the molybdenite Re-Os model ages ranging from 226 ± 3 to 228 ± 3 Ma. The Triassic monzogranite and granite porphyry belong to high-K calc-alkaline series and are characterized by high SiO2 and Al2O3 and low MgO, TiO2, and P2O5 concentrations, with negative Eu anomalies (δEu = 0.55-0.91). The least-altered monzogranite and granite porphyry yield uniform ɛ Nd( t) values from +1.6 to +3.6, and wide (87Sr/86Sr) i ratios ranging between 0.7035 and 0.7071, indicating that they were derived from the lower crust. In situ O-Hf isotopic analyses on zircon using SIMS and laser ablation multi-collector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) indicate that the δ18O and ɛ Hf( t) values of zircon from a monzogranite sample vary from 6.1 to 7.3 ‰ and +8.0 to +11.7, respectively, whereas zircon from a granite porphyry sample vary from 6.2 to 6.9 ‰ and +7.3 to +11.2, respectively. The geochemical and isotopic data imply that the primary magmas of the Baishan granite were likely derived from partial melts from the lower crust involving some mantle components. The Baishan Mo deposit and granitic emplacement were proposed to be most likely related to post-orogenic lithospheric extension and magmatic underplating. An extensional event coupled with the rising of hot mantle-derived melts triggered partial melting of the lower crust, as well as provided metals (Mo).

  15. Origin of Meso-Proterozoic post-collisional leucogranite suites (Kaokoveld, Namibia): constraints from geochronology and Nd, Sr, Hf, and Pb isotopes

    Science.gov (United States)

    Jung, S.; Mezger, K.; Nebel, O.; Kooijman, E.; Berndt, J.; Hauff, F.; Münker, C.

    2012-01-01

    Leucocratic granites of the Proterozoic Kaoko Belt, northern Namibia, now preserved as meta-granites, define a rock suite that is distinct from the surrounding granitoids based on their chemical and isotopic characteristics. Least evolved members of this ~1.5-1.6-Ga-old leucogranite suite can be distinguished from ordinary calc-alkaline granites that occur elsewhere in the Kaoko Belt by higher abundances of Zr, Y, and REE, more radiogenic initial ɛNd values and unradiogenic initial 87Sr/86Sr. The leucogranites have high calculated zircon saturation temperatures (mostly > 920°C for least fractionated samples), suggesting that they represent high-temperature melts originating from deep crustal levels. Isotope data (i.e., ɛNdi: +2.3 to -4.2) demonstrate that the granites formed from different sources and differentiated by a variety of processes including partial melting of mantle-derived meta-igneous rocks followed by crystal fractionation and interaction with older crustal material. Most fractionation-corrected Nd model ages (TDM) are between 1.7 and 1.8 Ga and only slightly older than the inferred intrusion age of ca. 1.6 Ga, indicating that the precursor rocks must have been dominated by juvenile material. Epsilon Hf values of zircon separated from two granite samples are positive (+11 and +13), and Hf model ages (1.5 and 1.6 Ga) are similar to the U-Pb zircon ages, again supporting the dominance of juvenile material. In contrast, the Hf model ages of the respective whole rock samples are 2.3 and 2.4 Ga, demonstrating the involvement of older material in the generation of the granites. The last major tectonothermal event in the Kaoko Belt in the Proterozoic occurred at ca. 2.0 Ga and led to reworking of mostly 2.6-Ga-old rocks. However, the presence of 1.6 Ga "post-collisional" granites reflects addition of some juvenile mantle-derived material after the last major tectonic event. The results suggest that similar A-type leucogranites are potentially more

  16. Multiple magma evolution and ore-forming processes of the Hongge layered intrusion, SW China: Insights from Sr-Nd isotopes, trace elements and platinum-group elements

    Science.gov (United States)

    Liao, Mingyang; Tao, Yan; Song, Xieyan; Li, Yubang; Xiong, Feng

    2015-12-01

    The Hongge layered intrusion (259 Ma), which is located in the inner zone of the Emeishan large igneous province (ELIP), is one of the most typical Fe-Ti-V ore deposits in the Pan-Xi area. Mafic-ultramafic layered intrusions of the ELIP have attracted a lot of attention lately because these intrusions host world class Fe-Ti-V oxide deposits plus interesting Cu-Ni-(PGE) mineralization which may have economic potential. This paper, reports new whole-rock major and trace element compositions, PGE abundances and Sr-Nd isotopic data for selected cumulate rocks and basalts. We use these data to investigate the nature of parental magmas and the controls on its evolution from the source mantle en route to the surface involving the Hongge ore-bearing intrusion. Two abrupt changes in Mt/Ilm and trace element ratios such as Ba/Th with depths in the Hongge layered intrusion indicate that this intrusion formed by at least two pluses of relatively primitive magma. The whole rock Sr-Nd isotopic data of basaltic and intrusive rocks plot in the region of Emeishan low-Ti basalts and the compositions of residual liquid (at ∼1260 °C and 1155 °C) calculated by MELTS are similar to our actual high-Ti (BFQ-2) and low-Ti (BC-1) basltic samples, indicate they are co-magmatic rather than derivation from a distinct source. Total PGE abundances in the Hongge samples are extremely low, ranging from 0.5 to 10 ppb. Sulfide-bearing rocks in the Hongge intrusion and the nearby coeval Banfangqing and Baicao basalts have similar mantle-like Pd/Pt ratios (2-6) and extremely high Cu/Pd ratios (3 × 104 to 4 × 105), indicating that sulfide segregation took place at depth prior to emplacement at Hongge and eruption in this region. Sulfide saturation in the Hongge magma may have resulted from such crustal contamination event. Crystallization of silicate minerals under the anhydrous magma, magma hydration plus Fe-Ti enrichments in the parental magma are three critical factors for the formation of Fe

  17. Geological, geochronological, geochemical, and Sr-Nd-O-Hf isotopic constraints on origins of intrusions associated with the Baishan porphyry Mo deposit in eastern Tianshan, NW China

    Science.gov (United States)

    Wang, Yinhong; Xue, Chunji; Liu, Jiajun; Zhang, Fangfang

    2016-03-01

    The Baishan porphyry Mo deposit (0.72 Mt; 0.06 % Mo) is located in the interior of the eastern Tianshan orogenic belt in Xinjiang, NW China. The deposit comprises 15 orebodies that are associated with monzogranite and granite porphyry stocks and are structurally controlled by roughly EW-trending faults. Secondary ion mass spectrometry (SIMS) zircon U-Pb dating of the monzogranite and granite porphyry yielded the Middle Triassic age (228 ± 2 to 227 ± 2 Ma), which coincide with the molybdenite Re-Os model ages ranging from 226 ± 3 to 228 ± 3 Ma. The Triassic monzogranite and granite porphyry belong to high-K calc-alkaline series and are characterized by high SiO2 and Al2O3 and low MgO, TiO2, and P2O5 concentrations, with negative Eu anomalies (δEu = 0.55-0.91). The least-altered monzogranite and granite porphyry yield uniform ɛ Nd(t) values from +1.6 to +3.6, and wide (87Sr/86Sr) i ratios ranging between 0.7035 and 0.7071, indicating that they were derived from the lower crust. In situ O-Hf isotopic analyses on zircon using SIMS and laser ablation multi-collector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) indicate that the δ18O and ɛ Hf(t) values of zircon from a monzogranite sample vary from 6.1 to 7.3 ‰ and +8.0 to +11.7, respectively, whereas zircon from a granite porphyry sample vary from 6.2 to 6.9 ‰ and +7.3 to +11.2, respectively. The geochemical and isotopic data imply that the primary magmas of the Baishan granite were likely derived from partial melts from the lower crust involving some mantle components. The Baishan Mo deposit and granitic emplacement were proposed to be most likely related to post-orogenic lithospheric extension and magmatic underplating. An extensional event coupled with the rising of hot mantle-derived melts triggered partial melting of the lower crust, as well as provided metals (Mo).

  18. Interaction between ultrapotassic magmas and carbonate rocks: Evidence from geochemical and isotopic (Sr, Nd, O) compositions of granular lithic clasts from the Alban Hills Volcano, Central Italy

    Science.gov (United States)

    Peccerillo, Angelo; Federico, Marcella; Barbieri, Mario; Brilli, Mauro; Wu, Tsai-Wan

    2010-05-01

    Magma-carbonate rock interaction is investigated through a geochemical and Sr-Nd-O isotope study of granular lithic clasts ( ejecta) from the Alban Hills ultrapotassic volcano, Central Italy. Some samples (Group-1) basically represent intrusive equivalents of Alban Hills magmas. A few samples (Group-2) are ultramafic, have high MgO (˜30 to 40 wt%) and δ 18O‰, and originated by accumulation of mafic phases that crystallised from ultrapotassic melts during assimilation of dolomitic rocks. Group-3 ejecta consist of dominant K-feldspar, and show major element compositions similar to phonolites, which, however, are absent among the Alban Hills volcanics. Finally, another group (Group-4) contains corroded K-feldspars, surrounded by a microgranular to porphyritic matrix, made of igneous minerals (K-feldspar, foids, clinopyroxene, phlogopite) plus wollastonite, garnet, and some cuspidine. Group-4 ejecta are depleted in SiO 2 and enriched in CaO with respect to Group-3. The analysed ejecta have similar 143Nd/ 144Nd (0.51204-0.51217) as the Alban Hills lavas, whereas 87Sr/ 86Sr (0.70900-0.71067) is similar to lower. Whole rocks δ 18O‰ ranges from +7.0 to +13.2, reaching maximum values in ultramafic samples. A positive correlation with CaO is observed in single rock groups. Large Ion Lithophile Element (LILE) abundances and REE fractionation are generally high, and extreme values of Th, U and LREE are found in some Group-3 and Group-4 rocks. Mineralogical, petrological and geochemical data reveal extensive interaction between magma and carbonate wall rocks, involving both dolostones and limestones. These processes had dramatic effects on magma compositions, especially on phonolites, which were transformed to foidites. Evidence of such a process is found in Group-4 samples, in which K-feldspar is observed to react with a matrix that represents strongly undersaturated melts formed by interaction between silicate magma and carbonates. Trace element data also testify to a

  19. Midcontinent rift volcanism in the Lake Superior region: Sr, Nd, and Pb isotopic evidence for a mantle plume origin

    Science.gov (United States)

    Nicholson, S.W.; Shirey, S.B.

    1990-01-01

    Between 1091 and 1098 Ma, most of a 15- to 20-km thickness of dominantly tholeiitic basalt erupted in the Midcontinent Rift System of the Lake Superior region, North America. The Portage Lake Volcanics in Michigan, which are the younget MRS flood basalts, fall into distinctly high- and low-TiO2 types having different liquid lines of descent. Incompatible trace elements in both types of tholeiites are enriched compared to depleted or primitive mantle and both basalt types are isotopically indistinguishable. The isotopic enrichment of the MRS source compared to depleted mantle is striking and must have occurred at least 700 m.y. before 1100 Ma. There are two likely sources for such magmatism: subcontinental lithospheric mantle enriched during the early Proterozoic or enriched mantle derived from an upwelling plume. Decompression melting of an upwelling enriched mantle plume in a region of lithosphere thinned by extension could have successfully generated the enormous volume (850 ?? 103 km3) of relatively homogeneous magma in a restricted time interval. -from Authors

  20. Determination of δ88/86Sr Using Matrix Correction by MC-ICP-MS

    Science.gov (United States)

    Zhu, B.; Yang, T.; Bian, X. P.; Zhu, Z. Y.

    2014-12-01

    Stable Sr isotopic compositions (δ88/86Sr) in marine carbonates potentially provide key information on paleoseawater temperature (Rüggeberg et al. 2008). Traditional methods for δ88/86Sr determination by 87Sr-84Sr double-spike TIMS or MC-ICP-MS require chemical purification of Sr before spectrometric measurements because of matrix effects. Recent studies suggested that the matrix-matching method, in which matrix-matched standard solutions were used to bracket untreated water samples, gave precise and accurate results for sulfur isotopic ratios by MC-ICP-MS (Lin et al., 2014). The obvious advantage of this method is that there is no need for chemical purification, thus eliminating the possibility of isotope fractionation during the ion chromatography and expediting sample throughput. In this study, we applied the matrix-matching method to δ88/86Sr determination by MC-ICP-MS. NIST 987 Sr solution and a purified seawater sample (collected from the South China Sea) were selected for this study. Given that major matrices in carbonate come form Ca2+, NIST 987 and SW solutions containing 40 ppm Ca2+ were prepared by adding high-purity Ca solution. All solutions used contained 200 ppb Sr and the 88Sr/86Sr ratios were measured using a Neptune MC-ICP-MS. The purified SW was first determined using SSB method, in which pure NIST 987 was used as standard to bracket SW and yielded δ88/86Sr value of 0.366 ± 0.008‰ (2SE, n = 10). The δ88/86Sr values of Ca-bearing SW were then measured by using pure NIST 987 solution as the working standard to investigate matrix effects. The determined δ88/86Sr value (0.039 ± 0.021‰; 2SE, n = 10) deviated obviously from the reference value. Finally, the matrix-matched NIST 987 was applied as the working standard to bracket the Ca-bearing SW, and the measured δ88/86Sr value is 0.351 ± 0.009‰ (2SE, n = 10), consistent with the reference value within uncertainties. The consistent δ88/86Sr values and comparable external precision

  1. Trace element and Sr-Nd-Pb isotope geochemistry of Rungwe Volcanic Province, Tanzania: Implications for a superplume source for East Africa Rift magmatism

    Directory of Open Access Journals (Sweden)

    Paterno R Castillo

    2014-09-01

    Full Text Available The recently discovered high, plume-like 3He/4He ratios at Rungwe Volcanic Province (RVP in southern Tanzania, similar to those at the Main Ethiopian Rift in Ethiopia, strongly suggest that magmatism associated with continental rifting along the entire East African Rift System (EARS has a deep mantle contribution (Hilton et al., 2011. New trace element and Sr-Nd-Pb isotopic data for high 3He/4He lavas and tephras from RVP can be explained by binary mixing relationships involving Early Proterozoic (+/- Archaean lithospheric mantle, present beneath the southern EARS, and a volatile-rich carbonatitic plume with a limited range of compositions and best represented by recent Nyiragongo lavas from the Virunga Volcanic Province also in the Western Rift. Other lavas from the Western Rift and from the southern Kenya Rift can also be explained through mixing between the same endmember components. In contrast, lavas from the northern Kenya and Main Ethiopian rifts can be explained through variable mixing between the same mantle plume material and the Middle to Late Proterozoic lithospheric mantle, present beneath the northern EARS. Thus, we propose that the bulk of EARS magmatism is sourced from mixing among three endmember sources: Early Proterozoic (+/- Archaean lithospheric mantle, Middle to Late Proterozoic lithospheric mantle and a volatile-rich carbonatitic plume with a limited range of compositions. We propose further that the African Superplume, a large, seismically anomalous feature originating in the lower mantle beneath southern Africa, influences magmatism throughout eastern Africa with magmatism at RVP and Main Ethiopian Rift representing two different heads of a single mantle plume source. This is consistent with a single mantle plume origin of the coupled He-Ne isotopic signatures of mantle-derived xenoliths and/or lavas from all segments of the EARS (Halldorsson et al., 2014.

  2. Target rocks, impact glasses, and melt rocks from the Lonar crater, India: Highly siderophile element systematics and Sr-Nd-Os isotopic signatures

    Science.gov (United States)

    Schulz, Toni; Luguet, Ambre; Wegner, Wencke; Acken, David; Koeberl, Christian

    2016-07-01

    The Lonar crater is a ~0.57-Myr-old impact structure located in the Deccan Traps of the Indian peninsula. It probably represents the best-preserved impact structure hosted in continental flood basalts, providing unique opportunities to study processes of impact cratering in basaltic targets. Here we present highly siderophile element (HSE) abundances and Sr-Nd and Os isotope data for target basalts and impactites (impact glasses and impact melt rocks) from the Lonar area. These tools may enable us to better constrain the interplay of a variety of impact-related processes such as mixing, volatilization, and contamination. Strontium and Nd isotopic compositions of impactites confirm and extend earlier suggestions about the incorporation of ancient basement rocks in Lonar impactites. In the Re-Os isochron plot, target basalts exhibit considerable scatter around a 65.6 Myr Re-Os reference isochron, most likely reflecting weathering and/or magma replenishment processes. Most impactites plot at distinctly lower 187Re/188Os and 187Os/188Os ratios compared to the target rocks and exhibit up to two orders of magnitude higher abundances of Ir, Os, and Ru. Moreover, the impactites show near-chondritic interelement ratios of HSE. We interpret our results in terms of an addition of up to 0.03% of a chondritc component to most impact glasses and impact melt rocks. The magnitude of the admixture is significantly lower than the earlier reported 12-20 wt% of extraterrestrial component for Lonar impact spherules, reflecting the typical difference in the distribution of projectile component between impact glass spherules and bulk impactites.

  3. Chapter 9 The magma feeding system of Somma-Vesuvius (Italy) strato-volcano: new inferences from a review of geochemical and Sr, Nd, Pb and O isotope data

    Science.gov (United States)

    Piochi, M.; de Vivo, B.; Ayuso, R.A.

    2006-01-01

    A large database of major, trace and isotope (Sr, Nd, Pb, O) data exists for rocks produced by the volcanic activity of Somma-Vesuvius volcano. Variation diagrams strongly suggest a major role for evolutionary processes such as fractional crystallization, contamination, crystal trapping and magma maxing, occurring after magma genesis in the mantle. Most mafic magmas are enriched in LILE (Light Ion Lithophile Elements; K. Rb, Ba), REE (Ce, Sm) and Y, show small Nb-Ta negative anomalies, and have values of Nb/Zr at about 0.15. Enrichments in LILE, REE, Nb and Ta do not correlate with Sr isotope values or degree of both K enrichment and silica undersaturation. The results indicate mantle source heterogeneity produced by slab-derived components beneath the volcano. However, the Sr isotope values of Somma-Vesuvius increase from 0.7071 up to 0.7081 with transport through the uppermost 11-12 km of the crust. The Sr isotope variation suggests that the crustal component affected the magmas during ascent through the lithosphere to the surface. Our new geochemical assessment based on chemical, isotopic and fluid inclusion data points to the existence of three main levels of magma storage. Two of the levels are deep and may represent long-lived reservoirs; the uppermost crustal level probably coincides with the volcanic conduit. The deeper level of magma storage is deeper than 12 km and fed the 1944 AD eruption. The intermediate level coincides with the seismic discontinuity detected by Zollo et al. (1996) at about 8 km. This intermediate level supplies magmas with 87Sr/86Sr values between 0.7071 and 0.7074, and ??O18erupted both during interplinian (i.e. 1906 AD) and sub-plinian (472 AD, 1631 AD) events. The shallowest level of magma storage at about 5 km was the site of magma chambers for the Pompei and Avellino plinian eruptions. New investigations are necessary to verify the proposed magma feeding system. ?? 2006 Elsevier B.V. All rights reserved.

  4. Accurate Quantification of Selenoprotein P (SEPP1) in Plasma Using Isotopically Enriched Seleno-peptides and Species-Specific Isotope Dilution with HPLC Coupled to ICP-MS/MS.

    Science.gov (United States)

    Deitrich, Christian L; Cuello-Nuñez, Susana; Kmiotek, Diana; Torma, Frank Attila; Del Castillo Busto, Maria Estela; Fisicaro, Paola; Goenaga-Infante, Heidi

    2016-06-21

    A novel strategy for the absolute quantification of selenium (Se) included in selenoprotein P (SEPP1), an important biomarker for human nutrition and disease, including diabetes and cancer, is presented here for the first time. It is based on the use of species-specific double isotope dilution mass spectrometry (SSIDA) in combination with HPLC-ICP-MS/MS for the determination of protein bound Se down to the peptide level in a complex plasma matrix with a total content of Se of 105.5 μg kg(-1). The method enabled the selective Se speciation analysis of human plasma samples without the need of extensive cleanup or preconcentration steps as required for traditional protein mass spectrometric approaches. To assess the method accuracy, two plasma reference materials, namely, BCR-637 and SRM1950, for which literature data and a reference value for SEPP1 have been reported, were analyzed using complementary hyphenated methods and the species-specific approach developed in this work. The Se mass fractions obtained via the isotopic ratios (78)Se/(76)Se and (82)Se/(76)Se for each of the Se-peptides, namely, ENLPSLCSUQGLR (ENL) and AEENITESCQUR (AEE) (where U is SeCys), were found to agree within 2.4%. A relative expanded combined uncertainty (k = 2) of 5.4% was achieved for a Se (as SEPP1) mass fraction of approximately 60 μg kg(-1). This work represents a systematic approach to the accurate quantitation of plasma SEPP1 at clinical levels using SSIDA quantification. Such methodology will be invaluable for the certification of reference materials and the provision of reference values to clinical measurements and clinical trials. PMID:27108743

  5. Crystal recycling in the steady-state system of the active Stromboli volcano : a 2.5-ka story inferred from in situ Sr-isotope and trace element data.

    OpenAIRE

    Francalanci, Lorella; Avanzinelli, Riccardo; Nardini, Isabella; Tiepolo, Massimo; Davidson, Jon P.; Vannucci, Riccardo

    2011-01-01

    In situ Sr-isotope data by microdrilling, cou- pled with major and trace element analyses, have been performed on plagioclase and clinopyroxene from seven samples collected during the 2002–2003 eruptive crisis at Stromboli volcano (Aeolian Islands, Italy). On 28 December 2002, the persistent moderate explosive activity was broken by an effusive event lasting about 7 months. A more violent explosion (paroxysm) occurred on 5 April 2003. Two magma types were erupted, namely a volatile- poor and ...

  6. Use of Pb and Sr isotopes as tracers of anthropogenic and natural inputs in rain waters and rivers of the Paris basin

    International Nuclear Information System (INIS)

    The isotopic composition of Pb and Sr, measured in the soluble phase of rain waters and rivers are used to determine and quantify the anthropogenic inputs and the weathering rates in the Seine basin. Atmospheric lead from rain waters is exclusively anthropogenic and is derived from gasoline and industrial emissions. These rain waters transfer lead, and certain other heavy metals, into the Seine, where the anthropogenic signal perturbs the natural geochemical cycle of these metals. This transfer to the river occurs principally in the city of Paris, in contrast, in the catchment area upstream of Paris, these elements are mainly trapped in soils, rather than transferred to the river. The anthropogenic inputs comprise three-quarters of the total transport of these metals by the Seine. In the river, lead transport is due to adsorption process occurring within the suspended load. Thus, soluble lead concentrations are linked to the river flow and the intensity of mechanical erosion. After correction for atmospheric and anthropogenic inputs, it is possible to estimate the silicate weathering rate for the Seine basin. This estimate is close to that obtained for large plain rivers, such as the Congo or Amazon, indicating that chemical erosion is linked to tectonic processes rather than climatic conditions. (author)

  7. Petrogenesis of Tarom high-potassic granitoids in the Alborz-Azarbaijan belt, Iran: Geochemical, U-Pb zircon and Sr-Nd-Pb isotopic constraints

    Science.gov (United States)

    Nabatian, Ghasem; Ghaderi, Majid; Neubauer, Franz; Honarmand, Maryam; Liu, Xiaoming; Dong, Yunpeng; Jiang, Shao-Yong; von Quadt, Albrecht; Bernroider, Manfred

    2014-01-01

    Large-scale Upper Eocene plutons in the Western Alborz-Azarbaijan orogenic belt mostly show calc-alkaline and I-type geochemical features contrasted by the Tarom complex with its high-potassic to shoshonitic affinity. The pluton was emplaced in the Tarom subzone of the orogenic belt and its laser ICP-MS zircon U-Pb age of 41 Ma is interpreted as the age of magma crystallization. The Tarom complex is composed of quartz monzodiorite, quartz-monzonite and monzogranite, the SiO2 contents range from 57 to 70 wt.%, the K2O + Na2O content is high (5.0-8.9 wt.%) and K2O/Na2O ratio ranges from 0.4 to 1.9. All the investigated rocks are enriched in light rare earth elements (LREEs), large ion lithophile elements (LILEs) and depleted in high field strength elements (HFSEs), and bear a weak Eu anomaly (Eu/Eu* = 0.46 to 1.38) in chondrite-normalized trace element patterns. The samples display some variety in initial Sr and Nd isotopic compositions, marked with low ISr = 0.704-0.705 and ɛNd (40 Ma) = - 4.2 to + 3.4 (- 5.7 for an enclave) values. The Pb isotopic ratios are (206Pb/204Pb) = 18.52-18.86, (207Pb/204Pb) = 15.57-15.72 and (208Pb/204Pb) = 38.47-39.08. Comparison with experimental studies, together with mantle-like isotopic ratios and comparisons of REE patterns, points to an origin of chemically enriched lithospheric mantle source for the Tarom plutonic complex. Partial melting process involving different partial melting degrees affecting heterogeneously metasomatized mantle is a process that seems likely to have occurred in the studied complex as the major differentiation process. The Tarom monzonitic plutons are considered to be post-orogenic intrusions that were emplaced in an environment of lithospheric extension, causing asthenospheric upwelling. Asthenospheric upwelling induced a thermal anomaly which caused partial melting of metasomatized subcontinental lithospheric mantle in the Tarom area.

  8. /sup 87/Sr//sup 86/Sr ratios for basalt from Loihi Seamount, Hawaii

    Energy Technology Data Exchange (ETDEWEB)

    Lanphere, M. (Geological Survey, Menlo Park, CA (USA))

    1983-12-01

    /sup 87/Sr//sup 86/Sr ratios of 15 samples of basalt dredged from Loihi Seamount range from 0.70334 to 0.70368. The basalt types range from tholeiite to basanite in composition and can be divided into six groups on the basis of abundances of K/sub 2/O, Na/sub 2/O, Rb and Sr and /sup 87/Sr//sup 86/Sr ratio. The isotopic data require that the various basalt types be derived from source regions differing in Sr isotopic composition. The Loihi basalts may be produced by mixing of isotopically distinct sources, but the tholeiites and alkalic basalts from Loihi do not show a well-developed inverse trend between Rb/Sr and /sup 87/Sr//sup 86/Sr that is characteristic of the later stages of Hawaiian volcanoes such as Haleakala and Koolau.

  9. The Messinian marine to nonmarine gypsums of Jumilla (Northern Betic Cordillera, SE Spain): Isotopic and Sr concentration constraints on the origin of parent brines

    Science.gov (United States)

    Rossi, Carlos; Vilas, Lorenzo; Arias, Consuelo

    2015-10-01

    The origin of the Messinian Hoya de la Sima (HS) gypsum (Betic foreland) is constrained using 87Sr/86Sr, δ34S, Sr concentration, and petrographic data. The Lower and Middle HS units consist of subaqueous vertically-aligned and stromatolitic selenites, the latter containing unusual microbial depositional textures. The Upper Unit consists of very-shallow-water bioturbated lenticular gypsum with Paracamelus ichnites. 87Sr/86Sr and δ34S indicate precipitation from predominantly marine waters, with upward increasing continental influence. Mixing models between Messinian seawater and continental water that dissolved Triassic evaporites show that the percentages of seawater required to explain the measured 87Sr/86Sr are analogous to the percentages obtained using δ34S, supporting precipitation from such mixtures. 87Sr/86Sr and δ34S of Lower HS selenites resemble those of the Primary Lower Gypsum (PLG) of the Messinian Salinity Crisis (MSC), in both cases indicating precipitation from seawater-continental water mixtures in which most Sr and SO4 were supplied by Messinian seawater. In the Lower HS selenites, Sr concentrations indicate contributing continental waters with Sr/Ca ratios similar to seawater. However, Sr concentrations of PLG selenites from other Betic basins (Bajo Segura, Sorbas indicate parent waters with Sr/Ca ratios lower than seawater. If the Sr contents of the betic PLG selenites are representative, it is unlikely that the Lower HS selenites represent the PLG. However, we cannot completely discard that option since different LPG subbasins could have had variable Sr/Ca. The HS gypsums formed coevally to diapirism of Triassic evaporites, in a restricted lagoonal basin developed during or slightly after a phase of strike-slip faulting in the Betic Cordillera. More general implications of this work are that Sr concentrations, combined with 87Sr/86Sr and δ34S data, provide key constraints on the origin of parent brines, and using Sr concentrations as

  10. Bayesian Integration of Isotope Ratios for Geographic Sourcing of Castor Beans

    Energy Technology Data Exchange (ETDEWEB)

    Webb-Robertson, Bobbie-Jo M.; Kreuzer, Helen W.; Hart, Garret L.; Ehleringer, James; West, Jason B.; Gill, Gary A.; Duckworth, Douglas C.

    2012-08-15

    Recent years have seen an increase in the forensic interest associated with the poison ricin, which is extracted from the seeds of the Ricinus communis plant. Both light element (C, N, O, and H) and strontium (Sr) isotope ratios have previously been used to associate organic material with geographic regions of origin. We present a Bayesian integration methodology that can more accurately predict the region of origin for a castor bean than individual models developed independently for light element stable isotopes or Sr isotope ratios. Our results demonstrate a clear improvement in the ability to correctly classify regions based on the integrated model with a class accuracy of 6 0 . 9 {+-} 2 . 1 % versus 5 5 . 9 {+-} 2 . 1 % and 4 0 . 2 {+-} 1 . 8 % for the light element and strontium (Sr) isotope ratios, respectively. In addition, we show graphically the strengths and weaknesses of each dataset in respect to class prediction and how the integration of these datasets strengthens the overall model.

  11. Repumping and spectroscopy of laser-cooled Sr atoms using the (5s5p){sup 3}P{sub 2}-(5s4d){sup 3}D{sub 2} transition

    Energy Technology Data Exchange (ETDEWEB)

    Mickelson, P G; De Escobar, Y N Martinez; Anzel, P; DeSalvo, B J; Nagel, S B; Traverso, A J; Yan, M; Killian, T C, E-mail: killian@rice.ed [Department of Physics and Astronomy, Rice University, Houston, TX 77251 (United States)

    2009-12-14

    We describe repumping and spectroscopy of laser-cooled strontium (Sr) atoms using the (5s5p){sup 3}P{sub 2}-(5s4d){sup 3}D{sub 2} transition. Atom number in a magneto-optical trap is enhanced by driving this transition because Sr atoms that have decayed into the (5s5p){sup 3}P{sub 2} dark state are repumped back into the (5s{sup 2}){sup 1}S{sub 0} ground state. Spectroscopy of {sup 84}Sr, {sup 86}Sr, {sup 87}Sr and {sup 88}Sr improves the value of the (5s5p){sup 3}P{sub 2}-(5s4d){sup 3}D{sub 2} transition frequency and determines the isotope shifts for the transition accurately enough to guide laser-cooling experiments with less abundant isotopes.

  12. Rb–Sr and Sm–Nd isotope systematics and geochemical studies on metavolcanic rocks from Peddavura greenstone belt: Evidence for presence of Mesoarchean continental crust in easternmost part of Dharwar Craton, India

    Indian Academy of Sciences (India)

    M Rajamanickam; S Balakrishnan; R Bhutani

    2014-07-01

    Linear, north–south trending Peddavura greenstone belt occurs in easternmost part of the Dharwar Craton. It consists of pillowed basalts, basaltic andesites, andesites (BBA) and rhyolites interlayered with ferruginous chert that were formed under submarine condition. Rhyolites were divided into type-I and II based on their REE abundances and HREE fractionation. Rb–Sr and Sm–Nd isotope studies were carried out on the rock types to understand the evolution of the Dharwar Craton. Due to source heterogeneity Sm–Nd isotope system has not yielded any precise age. Rb–Sr whole-rock isochron age of 2551 ± 19 (MSWD = 1.16) Ma for BBA group could represent time of seafloor metamorphism after the formation of basaltic rocks. Magmas representing BBA group of samples do not show evidence for crustal contamination while magmas representing type-II rhyolites had undergone variable extents of assimilation of Mesoarchean continental crust (< 3.3 Ga) as evident from their initial Nd isotope values. Trace element and Nd isotope characteristics of type I rhyolites are consistent with model of generation of their magmas by partial melting of mixed sources consisting of basalt and oceanic sediments with continental crustal components. Thus this study shows evidence for presence of Mesoarchean continental crust in Peddavura area in eastern part of Dharwar Craton.

  13. Zircon U-Pb dating, geochemical and Sr-Nd-Hf isotopic characteristics of the Jintonghu monzonitic rocks in western Fujian Province, South China: Implication for Cretaceous crust-mantle interactions and lithospheric extension

    Science.gov (United States)

    Li, Bin; Jiang, Shao-Yong; Lu, An-Huai; Zhao, Hai-Xiang; Yang, Tang-Li; Hou, Ming-Lan

    2016-09-01

    Comprehensive petrological, in situ zircon U-Pb dating, Ti-in-zircon temperature and Hf isotopic compositions, whole rock geochemical and Sr-Nd isotopic data are reported for the Jintonghu monzonitic intrusions in the western Fujian Province (Interior Cathaysia Block), South China. The Jintonghu monzonitic intrusions were intruded at 95-96 Ma. Their Sr-Nd-Hf isotopic compositions are similar to the coeval and nearby enriched lithospheric mantle-derived mafic and syenitic rocks, indicating that the Jintonghu monzonitic rocks were likely derived from partial melting of the enriched mantle sources. Their high Nb/Ta ratios (average 21.6) suggest that the metasomatically enriched mantle components were involved, which was attributed to the modification of slab-derived fluid and melt by the subduction of the paleo-Pacific Plate. The presence of mafic xenoliths, together with geochemical and isotopic features indicates a mafic-felsic magma mixing. Furthermore, the Jintonghu intrusions may have experienced orthopyroxene-, biotite- and plagioclase-dominated crystallization. Crust-mantle interaction can be identified as two stages, including that the Early Cretaceous mantle metasomatism and lithospheric extension resulted from the paleo-Pacific slab subduction coupled with slab rollback, and the Late Cretaceous crustal activation and enhanced extension induced by dip-angle subduction and the underplating of mantle-derived mafic magma.

  14. Single crystal U-Pb zircon age and Sr-Nd isotopic composition of impactites from the Bosumtwi impact structure, Ghana: Comparison with country rocks and Ivory Coast tektites.

    Science.gov (United States)

    Ferrière, Ludovic; Koeberl, Christian; Thöni, Martin; Liang, Chen

    2010-08-01

    The 1.07 Myr old Bosumtwi impact structure (Ghana), excavated in 2.1-2.2 Gyr old supracrustal rocks of the Birimian Supergroup, was drilled in 2004. Here, we present single crystal U-Pb zircon ages from a suevite and two meta-graywacke samples recovered from the central uplift (drill core LB-08A), which yield an upper Concordia intercept age of ca. 2145 ± 82 Ma, in very good agreement with previous geochronological data for the West African Craton rocks in Ghana. Whole rock Rb-Sr and Sm-Nd isotope data of six suevites (five from inside the crater and one from outside the northern crater rim), three meta-graywacke, and two phyllite samples from core LB-08A are also presented, providing further insights into the timing of the metamorphism and a possibly related isotopic redistribution of the Bosumtwi crater rocks. Our Rb-Sr and Sm-Nd data show also that the suevites are mixtures of meta-greywacke and phyllite (and possibly a very low amount of granite). A comparison of our new isotopic data with literature data for the Ivory Coast tektites allows to better constrain the parent material of the Ivory Coast tektites (i.e., distal impactites), which is thought to consist of a mixture of metasedimentary rocks (and possibly granite), but with a higher proportion of phyllite (and shale) than the suevites (i.e., proximal impactites). When plotted in a Rb/Sr isochron diagram, the sample data points (n = 29, including literature data) scatter along a regression line, whose slope corresponds to an age of 1846 ± 160 Ma, with an initial Sr isotope ratio of 0.703 ± 0.002. However, due to the extensive alteration of some of the investigated samples and the lithological diversity of the source material, this age, which is in close agreement with a possible "metamorphic age" of ∼ 1.8-1.9 Ga tentatively derived from our U-Pb dating of zircons, is difficult to consider as a reliable metamorphic age. It may perhaps reflect a common ancient source whose Rb-Sr isotope

  15. Single crystal U-Pb zircon age and Sr-Nd isotopic composition of impactites from the Bosumtwi impact structure, Ghana: Comparison with country rocks and Ivory Coast tektites.

    Science.gov (United States)

    Ferrière, Ludovic; Koeberl, Christian; Thöni, Martin; Liang, Chen

    2010-08-01

    The 1.07 Myr old Bosumtwi impact structure (Ghana), excavated in 2.1-2.2 Gyr old supracrustal rocks of the Birimian Supergroup, was drilled in 2004. Here, we present single crystal U-Pb zircon ages from a suevite and two meta-graywacke samples recovered from the central uplift (drill core LB-08A), which yield an upper Concordia intercept age of ca. 2145 ± 82 Ma, in very good agreement with previous geochronological data for the West African Craton rocks in Ghana. Whole rock Rb-Sr and Sm-Nd isotope data of six suevites (five from inside the crater and one from outside the northern crater rim), three meta-graywacke, and two phyllite samples from core LB-08A are also presented, providing further insights into the timing of the metamorphism and a possibly related isotopic redistribution of the Bosumtwi crater rocks. Our Rb-Sr and Sm-Nd data show also that the suevites are mixtures of meta-greywacke and phyllite (and possibly a very low amount of granite). A comparison of our new isotopic data with literature data for the Ivory Coast tektites allows to better constrain the parent material of the Ivory Coast tektites (i.e., distal impactites), which is thought to consist of a mixture of metasedimentary rocks (and possibly granite), but with a higher proportion of phyllite (and shale) than the suevites (i.e., proximal impactites). When plotted in a Rb/Sr isochron diagram, the sample data points (n = 29, including literature data) scatter along a regression line, whose slope corresponds to an age of 1846 ± 160 Ma, with an initial Sr isotope ratio of 0.703 ± 0.002. However, due to the extensive alteration of some of the investigated samples and the lithological diversity of the source material, this age, which is in close agreement with a possible "metamorphic age" of ∼ 1.8-1.9 Ga tentatively derived from our U-Pb dating of zircons, is difficult to consider as a reliable metamorphic age. It may perhaps reflect a common ancient source whose Rb-Sr isotope

  16. 87Sr/86Sr Concentrations in the Appalachian Basin: A Review

    Energy Technology Data Exchange (ETDEWEB)

    Mordensky, Stanley P. [Oak Ridge Inst. for Science and Education (ORISE), Oak Ridge, TN (United States); National Energy Technology Lab. (NETL), Albany, OR (United States); Lieuallen, A. Erin [Oak Ridge Inst. for Science and Education (ORISE), Oak Ridge, TN (United States); National Energy Technology Lab. (NETL), Albany, OR (United States); Verba, Circe [National Energy Technology Lab. (NETL), Albany, OR (United States); Hakala, Alexandra [National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States)

    2016-06-16

    This document reviews 87Sr/86Sr isotope data across the Appalachian Basin from existing literature to show spatial and temporal variation. Isotope geochemistry presents a means of understanding the geochemical effects hydraulic fracturing may have on shallow ground substrates. Isotope fractionation is a naturally occurring phenomenon brought about by physical, chemical, and biological processes that partition isotopes between substances; therefore, stable isotope geochemistry allows geoscientists to understand several processes that shape the natural world. Strontium isotopes can be used as a tool to answer an array of geological and environmental inquiries. In some cases, strontium isotopes are sensitive to the introduction of a non-native fluid into a system. This ability allows strontium isotopes to serve as tracers in certain systems. Recently, it has been demonstrated that strontium isotopes can serve as a monitoring tool for groundwater and surface water systems that may be affected by hydraulic fracturing fluids (Chapman et al., 2013; Kolesar Kohl et al., 2014). These studies demonstrated that 87Sr/86Sr values have the potential to monitor subsurface fluid migration in regions where extraction of Marcellus Shale gas is occurring. This document reviews publicly available strontium isotope data from 39 sample locations in the Appalachian Basin (Hamel et al., 2010; Chapman et al., 2012; Osborn et al., 2012; Chapman et al., 2013; Capo et al., 2014; Kolesar Kohl et al., 2014). The data is divided into two sets: stratigraphic (Upper Devonian/Lower Mississippi, Middle Devonian, and Silurian) and groundwater. ArcMap™ (ESRI, Inc.) was used to complete inverse distance weighting (IDW) analyses for each dataset to create interpolated surfaces in an attempt to find regional trends or variations in strontium isotopic values across the Appalachian Basin. 87Sr/86Sr varies up to ~ 0.011 across the

  17. 东天山白石泉镁铁-超镁铁杂岩体的Nd-Sr-Os同位素成分及其对岩浆演化的意义%Nd-Sr-Os isotopic data of the Baishiquan mafic-ultramafic complex from East Tianshan, and implications for petrogenesis

    Institute of Scientific and Technical Information of China (English)

    陈斌; 贺敬博; 陈长健; 木合塔尔·扎日

    2013-01-01

    本文报道东天山有铜镍硫化物矿化的白石泉镁铁-超镁铁杂岩体(分布在中天山地块北部)的微量元素和Nd-Sr-Os同位素成分,以探讨其地幔源区性质和壳幔相互作用过程.白石泉杂岩体的地球化学特征是富集大离子亲石元素和轻稀土元素,但亏损高场强元素.全岩Sr和Nd同位素初始比值变化较大,分别是(87Sr/86Sr)i =0.7032~0.7066和εNd(t)=5.6~-0.9,两者呈反相关关系.全岩Os含量在80×10-12~29×10-12之间,富含放射性成因Os(187 Os/188 Os=0.295~ 1.18).据此,得出结论:(1)白石泉杂岩体的母岩浆在上升侵位过程中,受到地壳物质的强烈混染,导致各岩石类型的Nd-Sr同位素成分变化很大和Os同位素成分富集放射性成因Os的特征,这与前人认为的白石泉岩体侵位过程中没有地壳混染作用的模式明显不同;(2)白石泉杂岩体的母岩浆来自被古生代俯冲带熔/流体交代过的年轻岩石圈地幔,这要求我们重新认识中天山前寒武地块的性质和规模.%We report trace elements and Nd-Sr-Os isotopic data for the Baishiquan mafic-ultramafic complex that occurs in the East Tianshan Mountains (in the northern part of the Mid-Tianshan Precambrian block) and is accompanied by Cu-Ni deposits, to understand its mantle source characteristics and processes of mantle-crustal interaction. Geochemically, the complex is characterized by enrichment of LILEs and depletion of HFSEs. The whole-rock Sr-Nd isotopic compositions of the Baishiquan complex vary significantly, with (87Sr/ 86Sr)i =0. 7032 ~0. 7066 and εNd(t) =5. 6 ~ -0. 9, and the Nd-Sr isotopic ratios are negatively correlated. The complex shows very radiogenic Os isotopic compositions, with (187Os/188Os)i =0.295~1. 18 and Os=80 ×l0-12 ~29 ×l0-12. Based on these data, we conclude that (1) the parent magma of the Baishiquan complex experienced significant crustal contamination during magma emplacement, as is revealed by the negatively

  18. A record of Late Quaternary continental weathering in the sediment of the Caspian Sea: evidence from U-Th, Sr isotopes, trace element and palynological data

    Science.gov (United States)

    Pierret, M. C.; Chabaux, F.; Leroy, S. A. G.; Causse, C.

    2012-09-01

    This study presents combined mineralogical, chemical, isotopic (87Sr/86Sr and U-Th disequilibria series) and palynological analyses on bulk sediments and on distinct mineral phases (carbonates and clays) from a 10-m-long core drilled in the southern Caspian Sea and containing a Late Pleistocene and Early Holocene record. The data allowed identifying 1) the main variations in sedimentation, 2) the processes causing these variations, 3) the modification of erosion vs weathering, and 4) the influence of climatic and/or Caspian Sea level changes in the region since the Late Pleistocene. The chemical and mineralogical results allowed the division of the sedimentary sequence into three main units and a transition zone. The lower unit (unit U1) primarily consists of silicate and carbonate-rich detritus. Sedimentation characteristics, including observation of detritus in secular equilibrium, are relatively constant within this unit and reflect mechanical erosion in a cold climate. Unit U1 probably corresponds to a glacial period when the vegetation cover was sparse and wind and river transport of pollen were strong. Subsequently, global increase in temperatures has greatly modified the sedimentation in the Caspian Sea south basin. Biogenic sedimentation is higher in units U2 and U3, and detrital inputs varied from unit U1. Variations in detrital input are likely to be caused by decreasing aeolian contribution and by relative changes in river volumes and origins. The study of the bulk sediments, clays and carbonates reflects an increase in chemical weathering since about 10 14C ka BP ago (base of unit U2), in line with an increase in the vegetation cover. Our results suggest an evolution of continental weathering conditions in the catchment area of the Caspian Sea, from dominantly mechanical/physical erosion during the cold period to a continuous increase in weathering since the Lateglacial period, as climate improved, which illustrates the strong relation between climate

  19. Important role of magma mixing in generating the Mesozoic monzodioritic-granodioritic intrusions related to Cu mineralization, Tongling, East China: evidence from petrological and in situ Sr-Hf isotopic data

    Science.gov (United States)

    Chen, Bin; Chen, ChangJian

    2016-04-01

    The Mesozoic ore-bearing high-Mg monzodioritic-granodioritic rocks in the Tongling mining district (East China) have been described as having adakitic affinities, and their origin has been attributed to partial melting of delaminated eclogite at depth in the mantle, followed by interaction of the resultant granitic magma with mantle peridotite. Here we present petrological data and in situ Sr isotopic data for zoned plagioclase that are inconsistent with the eclogite-derived model, and instead propose a model that involves magma mixing of siliceous crustal melts and basaltic magma that was derived from metasomatized mantle by subduction zone fluids in an extensional regime. The principal geochemical signatures of these Mesozoic rocks include a hydrous and high-K calc-alkaline affinity, high values of Mg#, high Sr abundances, high Sr/Y and La/Yb ratios, ɛNd(t)=-13.1 to -9.0, and ISr=0.70707-0.70824. The magma mixing model is supported by (1) the common existence of mafic microgranular enclaves (MMEs) and the disequilibrium textures of plagioclase and hornblende, (2) the increase in Ti and Al(IV) from hornblende cores to rims, and the overgrowths of high-Ca pyroxene around hornblende grains as well, indicative of episode of heating and rejuvenation of the magma chamber as a result of recharge of mafic magma, (3) the 87Sr/86Sr ratios of embayed high-Ca cores of plagioclase that are distinctly lower than in the euhedral low-Ca overgrowth rims, (4) negative correlations between whole-rock Nd and Sr isotopic ratios, and (5) the significant differences in the values of ɛHf(t) (-9.5 to -26) within different zircons from the same intrusion. We propose that underplating of hydrous basaltic magma from the metasomatized lithospheric mantle in the lower crust resulted in partial melting of the lower crustal rocks (Precambrian TTG gneisses and amphibolite/granulite) under water-saturated conditions, during which plagioclase decomposed, leaving hornblende-rich restites and

  20. Isotope-geochemical Nd-Sr evidence of Palaeoproterozoic plume magmatism in Fennoscandia and mantle-crust interaction on stages of layered intrusions formation

    Science.gov (United States)

    Serov, Pavel; Bayanova, Tamara; Kunakkuzin, Evgeniy; Steshenko, Ekaterina

    2016-04-01

    Palaeoproterozoic Fennoscandian layered intrusions belong to the pyroxenite-gabbronorite-anorthosite formation and spread on a vast area within the Baltic Shield. Based on isotope U-Pb, Sm-Nd, Rb-Sr and Re-Os data the duration of this formation can be to 100-130 Ma (2.53-2.40 Ga) [Serov et. al., 2008; Bayanova et. al., 2009]. We have studied rocks of layered PGE-bearing Fedorovo-Pansky, Monchetundra, Burakovsky, Olanga group intrusions and Penikat intrusion. According to recent and new complex Nd-Sr-REE data magma source of the vast majority of these intrusions was a mantle reservoir with unusual characteristics: negative values of ɛNd (from 0 to -4) and ISr = 0.702-0.706, flat spectra of REE (value of (La/Yb)N ~ 1.0-5.8) with positive Eu-anomalies [Bayanova et. al., 2009; Bayanova et. al., 2014]. However, the distribution of REE for ore-bearing gabbronorite intrusions Penikat (Sm-Nd age is 2426 ± 38 Ma [Ekimova et. al., 2011]) has a negative Eu-anomalies. This may be due to the formation of plagioclase and its removal from the magma chamber. One of the aims of isotope geochemical investigations is to establish the contribution of mantle components in the formation of layered intrusions rocks and the degrees of contamination of the magma source by crustal material. To calculate the proportion of mantle component model binary mixture was used [Jahn et. al., 2000]. As the mantle components we used data for CHUR: ɛNd = 0, [Nd] = 1.324 [Palm, O'Neil, 2003] and for crustal components were used host-rocks Nd-data. The proportion of mantle component for the studied intrusions was 77-99%. Also, data were obtained for the Monchetundra dike complex and amphibolized gabbro, for which the proportion of mantle material was 20-40%. For these rocks a significant crustal contamination is most likely. This process resulted in low values of ɛNd, a direct relationship between ɛNd and Nd concentration, and significant differences between the U-Pb and Sm-Nd model ages. A

  1. A Multi-Isotope (B, Sr, O, H, C) and Age Dating (3H-3He, 14C) Study of Ground Water From Salinas Valley, California: Hydrochemistry, Dynamics, and Contamination Processes

    Energy Technology Data Exchange (ETDEWEB)

    Vengosh, A; Gill, J; Davisson, M L; Hudson, B G

    2001-08-01

    The chemical and isotopic ({sup 11}B/{sup 10}B, {sup 87}Sr/{sup 86}Sr, {sup 18}O/{sup 16}O, {sup 2}H/H, {sup 13}C/{sup 12}C, {sup 14}C, {sup 3}He/{sup 3}H) compositions of groundwater from the upper aquifer system of the Salinas Valley in coastal central California were investigated in order to delineate the origin and processes of groundwater contamination in this complex system. The Salinas Valley has a relatively deep, confined ''400-foot'' aquifer, overlain by a ''180-foot'' aquifer, and a shallower perched aquifer, all made up of alluvial sand, gravel, and clay deposits. Groundwater from the aquifers have different {sup 14}C ages; fossil ({sup 14}C = 21.3 pmc) for the 400-foot, and modern ({sup 14}C = 72.2 to 98.2 pmc) for the 180-foot. Fresh groundwater in all aquifers is recharged naturally and artificially and through the Salinas River. The two modes of recharge can be distinguished chemically. We identified several different saline components with distinguishable chemical and isotopic fingerprints. (1) Salt-water intrusion in the northern basin has Cl concentrations up to 1700 mg/l, a Na/Cl ratio seawater, {delta}{sup 11}B between +17 and +38 per mil, and {sup 87}Sr/{sup 86}Sr between 0.7088 and 0.7096. Excess dissolved Ca, relative to the expected concentration for simple dilution of seawater, correlates with {sup 87}Sr/{sup 86}Sr ratios, suggesting base exchange reaction with clay minerals. (2) Agriculture return flow is high in NO{sub 3} and SO{sub 4}, with a {sup 87}Sr/{sup 86}Sr = 0.7082, {delta}{sup 11}B = 19 per mil; and {delta}{sup 13}C between -23 and -17 per mil. The {sup 3}H-{sup 3}He ages (5-17 years) and {sup 14}C data suggest vertical infiltration rates of irrigation water of 3 to 10 m/yr. (3) Non-marine saline water in the southern part of the valley has high TDS up to 3800 mg/l, high SO{sub 4}, Na/Cl ratio >1, {delta}{sup 11}B between +24 and +30 per

  2. Geochemical and Sr-Nd isotope variations within Cretaceous continental flood-basalt suites of the Canadian High Arctic, with a focus on the Hassel Formation basalts of northeast Ellesmere Island

    Science.gov (United States)

    Estrada, Solveig

    2015-11-01

    Early- to mid-Cretaceous flood-basalt suites of the northeast Canadian High Arctic assigned to a High Arctic Large Igneous Province (HALIP) were studied for their whole-rock geochemistry and Sr-Nd isotopes. Data from basalt flows within the upper Albian to lower Cenomanian Hassel Formation of northeast Ellesmere Island are compared with former published data and new inductively coupled plasma mass spectrometry data of the stratigraphic equivalent Strand Fiord basalts and the older, late Hauterivian to Aptian Isachsen basalts from Axel Heiberg Island. The transitional to mildly alkaline aphyric Hassel basalts, with ocean island basalt (OIB)-like geochemical signatures in parts, have an Ar-Ar whole-rock age of on average 96.4 ± 1.6 Ma. They represent two geochemically different flow units without a fractional crystallization relationship: the high-phosphorous (HP) and low-phosphorous (LP) basalts. The Hassel HP basalts differ from the LP basalts by additionally higher Ba, K, Rb, Th and LREE contents, a pronounced positive Eu anomaly (Eu/Eu* = 1.74-1.76), as well as lower Ta, Nb, Zr and Hf concentrations. The Nd and Sr isotope ratios of the Hassel HP basalts [ ɛ Nd( t) of -1.3 to -1.4, 87Sr/86Sr( t) of 0.70706-0.70707] and the LP basalts [ ɛ Nd( t) of 4.5-4.9, 87Sr/86Sr( t) of 0.7038-0.7040] indicate an origin from different mantle sources. The geochemically similar tholeiitic Isachsen (ca. 130-113 Ma) and Strand Fiord basalts (ca. 105-95 Ma) are also incompatible element enriched relative to the primitive mantle, however, with negative Sr-P anomalies as well as partially negative K, Ta and Nb anomalies. In terms of incompatible element ratios (Zr/Nb, Nb/Th), several mantle components are involved in the formation of the flood-basalt suites: a component with primitive mantle composition, an OIB-like component (probably subducted and recycled oceanic crust) and an enriched lithospheric component. The latter component, probably metasomatized subcontinental

  3. 88Sr/86Sr fractionation in inorganic aragonite and in corals

    Science.gov (United States)

    Fruchter, Noa; Eisenhauer, Anton; Dietzel, Martin; Fietzke, Jan; Böhm, Florian; Montagna, Paolo; Stein, Moti; Lazar, Boaz; Rodolfo-Metalpa, Riccardo; Erez, Jonathan

    2016-04-01

    Conflicting results have been reported for the stable Sr isotope fractionation, specifically with respect to the influence of temperature. In an experimental study we have investigated the stable Sr isotope systematics for inorganically precipitated and biogenic (coral) aragonite (natural and laboratory-cultured). Inorganic aragonite precipitation experiments were performed from natural seawater using the CO2 diffusion technique. The experiments were performed at different temperatures and different carbonate ion concentrations. 88Sr/86Sr of the inorganic aragonite precipitated in the experiments are 0.2‰ lighter than seawater, but showed no correlation to the water temperature or to CO32- concentration. Similar observations are made in different coral species (Cladocora caespitosa, Porites sp. and Acropora sp.), with identical fractionation from the bulk solution and no correlation to temperature or CO32- concentration. The lack of 88Sr/86Sr variability in corals at different environmental parameters and the similarity to the 88Sr/86Sr fractionation in inorganic aragonite may indicate a similar Sr incorporation mechanism in corals skeleton and inorganic aragonite, and therefore the previously proposed Rayleigh-based multi element model (Gaetani et al., 2011) cannot explain the process of Sr incorporation in the coral skeletal material. It is proposed that the relatively constant 88Sr/86Sr fractionation in aragonite can be used for paleo reconstruction of seawater 88Sr/86Sr composition. The seawater 88Sr/86Sr ratio reconstruction can be further used in calcite samples to reconstruct paleo precipitation rates.

  4. Efficient Separation and Accurate Isotopic Determination of Lithium in Brine%盐湖卤水中锂的高效分离及其同位素比值的精确测定进展

    Institute of Scientific and Technical Information of China (English)

    马茹莹; 韩凤清; 罗重光; 闫建平; 张燕霞

    2012-01-01

    The significant relative mass difference between the two stable isotopes of lithium makes a great lithium isotopic fractionation in nature materials. Lithium isotopes, as a tracer, have been used to indicate the material source and formation mechanism of lithium deposit. At present,the lithium isotope ratio was measured by thermal ionization mass spectrometry (TIMS) or the multiple collector inductively coupled plasma mass spectrometry ( MC-ICP-MS). Both methods require the lithium completely separated from other elements. The adsorption method, in all the lithium extractive technique,could produce higher recovery rate and minimize isotopic fractionation. This paper mainly introduced the progress of the separation and accurate isotopic determination of lithium in brine at home and abroad in recent years.%锂的两个稳定同位素相对质量差较大,导致了自然界中的锂同位素分馏强烈.卤水中锂同位素作为良好示踪剂,可用以指示盐湖锂矿床的物质来源和形成机理.现阶段一般用热电离质谱法(TIMS)或多接收器电感耦合等离子质谱法(MC-ICP-MS)测量锂同位素比值,这两种方法都需要将锂从样品中与其它元素完全分离.在现有的卤水提锂方法中,吸附法能够得到较高的锂回收率,减少了锂同位素在提取过程中的分馏效应.本文主要介绍国内外近年来在提取锂和准确测定锂同位素比值方面所取得的进展.

  5. Geochemistry and Sr-Nd isotopes of the subvolcanic sill complex and sandstone geochronology from María Magdalena island, Nayarit, Mexico

    Science.gov (United States)

    Villanueva, D.; Schaaf, P. E.; Hernandez, T.; Solis, G.; Weber, B.; Pompa, V.

    2013-12-01

    María Magdalena island is part of the Islas Marías archipielago, located at the mouth of the Gulf of California. Understanding the nature and origin of the archipelago is very important for reconstructing the paleoposition of Baja California Peninsula prior to the opening of the Gulf of California. We present the first geochemical, isotopic and geochronologic data from María Magdalena, a lithologically different island compared to the rest of the archipelago. María Magdalena island is located southeast of María Madre and northeast of María Cleofas islands and is composed by a sedimentary sequence of sandstones and minor shale, which is intruded by gabbroic sills. The sedimentary sequence dips approximately 20 degrees to the NW. The thickness of sills range from 1 to 3 meters with mineralogical variations of plagioclase +/- orthopyroxene +/- clinopyroxene +/- hornblende and some altered olivine crystals. Textures are mostly porphyritic with plagioclase crystals sizes up to 5 cm and olivines up to 5 mm. The gabbroic sills show SiO2 contents from 42.7 to 47.5 wt. %; TiO2 from 0.8 to 2 wt. %; Fe2O3t from 7.7 to 11.9 wt. %; MgO from 6.2 to 19.8 wt. % and of CaO from 6 to 11.6 wt. %, indicating mafic to ultramafic compositions. A multielement spider diagram as well as REE patterns show compositions very similar to N-MORB or even peridotites, which is confirmed by 87Sr/86Sr values from 0.70273 to 0.70497, and 143Nd/144Nd values from 0.513003 to 0.513100. U-Pb single zircon geochronology of the intruded sandstones display the following age distribution: eight crystals show ages from 80 to 86 Ma, three crystals have ages from 61 to 72 Ma, and three are around 21 Ma which constrains a maximum sandstone deposition age. Consequently, the sills must be younger than 21 Ma. There is not much lithological similarity with neighboring María Madre island to the NW (containing a metamorphic complex, granitoids and acid volcanic roks) and with María Cleofas island to the SE

  6. Erosion of the Alps: use of Rb-Sr isotopic data from molassic sediments to identify the ages of the metamorphism recorded by the eroded rocks; Erosion des Alpes: histoire metamorphique des roches erodees par l`analyse du couple Rb-Sr des sediments molassiques

    Energy Technology Data Exchange (ETDEWEB)

    Henry, P.; Deloule, E. [Centre National de la Recherche Scientifique (CNRS), 54 - Nancy (France). Centre de Recherches Petrographiques et Geochimiques; Michard, A. [Aix-Marseille-3 Univ., 13 - Marseille (France)

    1994-06-01

    Rb-Sr isotopic data from Oligocene and Miocene peri-alpine molassic sediments allow us to identify the different periods for which the eroded rocks have or have not recorded an alpine metamorphism. The Chattian and the Burdigalian sediments result from the erosion of rocks for which the latest metamorphic event was variscan, while the Stampian, Aquitanian and ``Helvetian`` sediments show evidence for the erosion of rocks which have recorded alpine metamorphic events. The application of this method to old detrital sediments could permit determination of the ages of the tectonic events which occurred in the sediment source regions. (authors). 18 refs., 6 figs.

  7. Influx of Different Galapagos Plume Components to the Galapagos Spreading Center: Evidence From Sr-Nd-Pb-Hf Isotope Variations in Axial Lavas Between 86W and 92.5W

    Science.gov (United States)

    Hauff, F.; Hanan, B.; Hoernle, K. A.; Kokfelt, T. F.; Christie, D.; Werner, R.

    2006-12-01

    We present new Sr-Nd-Pb-Hf isotope data of basaltic glasses from the GSC between 86W and 92.5W. In this part of the ridge the main structural inventory includes an overlapping spreading center (OSC) at 87.3W, a transform fault (TF) at 91W and a series of seamount chains intersecting the GSC West of the 91W TF. The systematic transition from an axial-valley and rift morphology at axial depths of 2450 m.b.s.l. in the 86W area to an axial-high morphology at progressively shallower depths of 1500 m.b.s.l in the 90.5W area together with gradational changes in major and trace element chemistry of the axial lavas is believed to reflect increasing mantle temperature and compositional changes related to the Galapagos plume [1]. Previous work from 83W to 105W revealed a broad symmetric gradational pattern at around 91W and lead to the conclusion that this region is the main point of plume influx on the GSC [2]. Based on published isotope data Christie et al. (2005) inferred the probable existence of two enrichment peaks immediately East and West of the 91TF. Indeed, along axis variations of our new Sr-Nd-Pb-Hf isotope data map two distinct peaks of enrichment at 92W and 90.5W, suggesting that mantle from the Galapagos hotspot enters the GSC melting zone on both sides of the 91W transform fault. Lavas from within the 91W TF are isotopically intermediate and show a distinct depletion in incompatible trace elements, which may reflect repeated melting at shallow depth of passively upwelling mantle in this unique extensional regime. At least three different components are required to generate the observed isotope correlations. When compared to the geographically distinct isotopic domains of the Galapagos islands; GSC lavas East of the 91W TF form tight correlations from the rim of the Central Galapagos domain through the Eastern Galapagos domain towards DMM. Most axial lavas and corresponding off axis seamounts West of the 91W TF have higher 87Sr/86Sr, 207Pb/204Pb, 208Pb/204Pb

  8. Constraints on the evolution of the Japan Sea based on 40Ar-39Ar ages and Sr isotopic ratios for volcanic rocks of the Yamato Seamount chain in the Japan Sea

    International Nuclear Information System (INIS)

    40Ar-39Ar and Sr isotope analyses were performed on basalts and andesites dredged from the Yamato Seamount chain in the Japan Sea. The 40Ar-39Ar plateau ages range from about 11 to 17 Ma, though most samples show ages between 10 and 14 Ma. The seamounts seem to have formed within a period of a few million years, although some of them might have formed earlier. Based on the present results together with previously reported radiometric age data, it is thought that the Yamato Basin formed during some period prior to 17 Ma and probably later than around 25 Ma. Taking into account the radiometric age data on rocks from the Japan Basin, it is conjectured that the opening of the Japan Sea might have started almost at this time or a little earlier. The observed 87Sr/86Sr ratios range from 0.70357 to 0.70388, suggesting incorporation of some time-integrated components enriched in incompatible elements such as continental crustal materials. This may indicate that in the Japan Sea area, at least the Yamato Basin had not developed enough to show the characteristics of typical N-type MORB source materials without being affected by pre-existing continental crustal materials. (orig.)

  9. Influence of bacteria on lanthanide and actinide transfer from specific soil components (humus, soil minerals and vitrified municipal solid waste incinerator bottom ash) to corn plants: Sr-Nd isotope evidence

    International Nuclear Information System (INIS)

    Experiments have been performed to test the stability of vitrified municipal solid waste (MSW) incinerator bottom ash under the presence of bacteria (Pseudomonas aeruginosa) and plants (corn). The substratum used for the plant growth was a humus-rich soil mixed with vitrified waste. For the first time, information on the stability of waste glasses in the presence of bacteria and plants is given. Results show that inoculated plant samples contained always about two times higher lanthanide and actinide element concentrations. Bacteria support the element transfer since plants growing in inoculated environment developed a smaller root system but have higher trace element concentrations. Compared with the substratum, plants are light rare earth element (LREE) enriched. The vitrified bottom ash has to some extent been corroded by bacteria and plant activities as indicated by the presence of Nd (REE) and Sr from the vitrified waste in the plants. 87Sr/86Sr and 143Nd/144Nd isotope ratios of plants and soil components allow the identification of the corroded soil components and confirm that bacteria accelerate the assimilation of elements from the vitrified bottom ash. These findings are of importance for landfill disposal scenarios, and similar experiments should be performed in order to better constrain the processes of microbially mediated alteration of the MSW glasses in the biosphere

  10. Influence of bacteria on lanthanide and actinide transfer from specific soil components (humus, soil minerals and vitrified municipal solid waste incinerator bottom ash) to corn plants: Sr-Nd isotope evidence

    Energy Technology Data Exchange (ETDEWEB)

    Aouad, Georges [Ecole et Observatoire des Sciences de la Terre, Centre de Geochimie de la Surface/CNRS UMR 7517, 1 rue Blessig, 67084 Strasbourg Cedex (France); Stille, Peter [Ecole et Observatoire des Sciences de la Terre, Centre de Geochimie de la Surface/CNRS UMR 7517, 1 rue Blessig, 67084 Strasbourg Cedex (France)]. E-mail: pstille@illite.u-strasbg.fr; Crovisier, Jean-Louis [Ecole et Observatoire des Sciences de la Terre, Centre de Geochimie de la Surface/CNRS UMR 7517, 1 rue Blessig, 67084 Strasbourg Cedex (France); Geoffroy, Valerie A. [UMR 7156 Universite Louis-Pasteur/CNRS, Genetique Moleculaire, Genomique Microbiologie, Departement Micro-organisme, Genomes, Environnement, 28 rue Goethe, 67083 Strasbourg Cedex (France); Meyer, Jean-Marie [UMR 7156 Universite Louis-Pasteur/CNRS, Genetique Moleculaire, Genomique Microbiologie, Departement Micro-organisme, Genomes, Environnement, 28 rue Goethe, 67083 Strasbourg Cedex (France); Lahd-Geagea, Majdi [Ecole et Observatoire des Sciences de la Terre, Centre de Geochimie de la Surface/CNRS UMR 7517, 1 rue Blessig, 67084 Strasbourg Cedex (France)

    2006-11-01

    Experiments have been performed to test the stability of vitrified municipal solid waste (MSW) incinerator bottom ash under the presence of bacteria (Pseudomonas aeruginosa) and plants (corn). The substratum used for the plant growth was a humus-rich soil mixed with vitrified waste. For the first time, information on the stability of waste glasses in the presence of bacteria and plants is given. Results show that inoculated plant samples contained always about two times higher lanthanide and actinide element concentrations. Bacteria support the element transfer since plants growing in inoculated environment developed a smaller root system but have higher trace element concentrations. Compared with the substratum, plants are light rare earth element (LREE) enriched. The vitrified bottom ash has to some extent been corroded by bacteria and plant activities as indicated by the presence of Nd (REE) and Sr from the vitrified waste in the plants. {sup 87}Sr/{sup 86}Sr and {sup 143}Nd/{sup 144}Nd isotope ratios of plants and soil components allow the identification of the corroded soil components and confirm that bacteria accelerate the assimilation of elements from the vitrified bottom ash. These findings are of importance for landfill disposal scenarios, and similar experiments should be performed in order to better constrain the processes of microbially mediated alteration of the MSW glasses in the biosphere.

  11. U-Pb zircon, geochemical and Sr-Nd-Hf-O isotopic constraints on age and origin of the ore-bearing intrusions from the Nurkazgan porphyry Cu-Au deposit in Kazakhstan

    Science.gov (United States)

    Shen, Ping; Pan, Hongdi; Seitmuratova, Eleonora; Jakupova, Sholpan

    2016-02-01

    Nurkazgan, located in northeastern Kazakhstan, is a super-large porphyry Cu-Au deposit with 3.9 Mt metal copper and 229 tonnage gold. We report in situ zircon U-Pb age and Hf-O isotope data, whole rock geochemical and Sr-Nd isotopic data for the ore-bearing intrusions from the Nurkazgan deposit. The ore-bearing intrusions include the granodiorite porphyry, quartz diorite porphyry, quartz diorite, and diorite. Secondary ion mass spectrometry (SIMS) zircon U-Pb dating indicates that the granodiorite porphyry and quartz diorite porphyry emplaced at 440 ± 3 Ma and 437 ± 3 Ma, respectively. All host rocks have low initial 87Sr/86Sr ratios (0.70338-0.70439), high whole-rock εNd(t) values (+5.9 to +6.3) and very high zircon εHf(t) values (+13.4 to +16.5), young whole-rock Nd and zircon Hf model ages, and consistent and slightly high zircon O values (+5.7 to +6.7), indicating that the ore-bearing magmas derived from the mantle without old continental crust involvement and without marked sediment contamination during magma emplacement. The granodiorite porphyry and quartz diorite porphyry are enriched in large ion lithophile elements (LILE) and light rare earth elements (LREE) and depleted in high-field strength elements (HFSE), Eu, Ba, Nb, Sr, P and Ti. The diorite and quartz diorite have also LILE and LREE enrichment and HFSE, Nb and Ti depletion, but have not negative Eu, Ba, Sr, and P anomalies. These features suggest that the parental magma of the granodiorite porphyry and quartz diorite porphyry originated from melting of a lithospheric mantle and experienced fractional crystallization, whereas the diorite and quartz diorite has a relatively deeper lithospheric mantle source region and has not experienced strong fractional crystallization. Based on these, together with the coeval ophiolites in the area, we propose that a subduction of the Balkhash-Junggar oceanic plate took place during the Early Silurian and the ore-bearing intrusions and associated Nurkazgan

  12. 90Sr liquid scintillation urine analysis utilizing different approaches for tracer recovery.

    Energy Technology Data Exchange (ETDEWEB)

    Piraner, Olga; Preston, Rose T.; Shanks, Sonoya Toyoko; Jones, Robert

    2010-08-01

    90Sr is one of the isotopes most commonly produced by nuclear fission. This medium lived isotope presents serious challenges to radiation workers, the environment, and following a nuclear event, the general public. Methods of identifying this nuclide have been in existence for a number of years (e.g. Horwitz, E.P. [1], Maxwell, S.L.[2], EPA 905.0 [3]) which are time consuming, requiring a month or more for full analysis. This time frame is unacceptable in the present security environment. It is therefore important to have a dependable and rapid method for the determination of Sr. The purposes of this study are to reduce analysis time to less than half a day by utilizing a single method of radiation measurement while continuing to yield precise results. This paper presents findings on three methods that can meet this criteria; (1) stable Sr carrier, (2) 85Sr by gamma spectroscopy, and (3) 85Sr by LSC. Two methods of analyzing and calculating the 85Sr tracer recovery were investigated (gamma spectroscopy and a low energy window-Sr85LEBAB by LSC) as well as the use of two different types of Sr tracer (85Sr and stable Sr carrier). Three separate stock blank urine samples were spiked with various activity levels of 239Pu, 137Cs, 90Sr /90Y to determine the effectiveness of the Eichrome Sr-spec resin 2mL extractive columns. The objective was to compare the recoveries of 85Sr versus a stable strontium carrier, attempt to compare the rate at which samples can be processed by evaluating evaporation, neutralization, and removing the use of another instrument (gamma spectrometer) by using the LSC spectrometer to obtain 85Sr recovery. It was found that when using a calibration curve comprised of a different cocktail and a non-optimum discriminator setting reasonable results (bias of « 25%) were achieved. The results from spiked samples containing 85Sr demonstrated that a higher recovery is obtained when using gamma spectroscopy (89-95%) than when using the LEB window

  13. 90Sr liquid scintillation urine analysis utilizing different approaches for tracer recovery.

    Energy Technology Data Exchange (ETDEWEB)

    Piraner, Olga [Centers for Disease Control and Prevention, Atlanta, GA; Preston, Rose T. [Sandia Staffing Alliance, LLC, Albuquerque, NM; Shanks, Sonoya Toyoko; Jones, Robert [Centers for Disease Control and Prevention, Atlanta, GA

    2010-08-01

    90Sr is one of the isotopes most commonly produced by nuclear fission. This medium lived isotope presents serious challenges to radiation workers, the environment, and following a nuclear event, the general public. Methods of identifying this nuclide have been in existence for a number of years (e.g. Horwitz, E.P. [1], Maxwell, S.L.[2], EPA 905.0 [3]) which are time consuming, requiring a month or more for full analysis. This time frame is unacceptable in the present security environment. It is therefore important to have a dependable and rapid method for the determination of Sr. The purposes of this study are to reduce analysis time to less than half a day by utilizing a single method of radiation measurement while continuing to yield precise results. This paper presents findings on three methods that can meet this criteria; (1) stable Sr carrier, (2) 85Sr by gamma spectroscopy, and (3) 85Sr by LSC. Two methods of analyzing and calculating the 85Sr tracer recovery were investigated (gamma spectroscopy and a low energy window-Sr85LEBAB by LSC) as well as the use of two different types of Sr tracer (85Sr and stable Sr carrier). Three separate stock blank urine samples were spiked with various activity levels of 239Pu, 137Cs, 90Sr /90Y to determine the effectiveness of the Eichrome Sr-spec%C2%AE resin 2mL extractive columns. The objective was to compare the recoveries of 85Sr versus a stable strontium carrier, attempt to compare the rate at which samples can be processed by evaluating evaporation, neutralization, and removing the use of another instrument (gamma spectrometer) by using the LSC spectrometer to obtain 85Sr recovery. It was found that when using a calibration curve comprised of a different cocktail and a non-optimum discriminator setting reasonable results (bias of %C2%B1 25%) were achieved. The results from spiked samples containing 85Sr demonstrated that a higher recovery is obtained when using gamma spectroscopy (89-95%) than when using the LEB window

  14. Origin of Mesozoic and Tertiary granite in the western United States and implications for Pre-Mesozoic crustal structure: 2. Nd and Sr isotopic studies of unmineralized and Cu- and Mo-mineralized granite in the Precambrian Craton

    Science.gov (United States)

    Farmer, G. Lang; Depaolo, Donald J.

    1984-11-01

    In the Cordilleran region of the western United States, Mesozoic and Tertiary peraluminous granitic rocks display regional variations in initial 143Nd/144Nd (ɛNd); ɛNd = -10 to -12 in southern Arizona, - 17 to -19 in the northern Great Basin (NGB), and -30 in the northern Rocky Mountains. Initial 87Sr/86Sr values are between 0.710 and 0.721 and show no regional pattern. Metaluminous granitic rocks have a wider range of ɛNd values extending from values similar to those of the peraluminous granites to much higher values. The 87Sr/86Sr values are mostly fairly low, between 0.705 and 0.710 except in the NGB where values as high as 0.7157 are observed. No systematic differences between the ɛNd or 87Sr/86Sr values of Cu- or Mo-mineralized and Unmineralized granite were discerned, except for Cu-mineralized granite in eastern Nevada and Mo-mineralized granite in Colorado, which have ɛNd values higher (˜0) and lower ( ˜-10.0), respectively, than Unmineralized granite in the same region. Comparison to ɛNd values of exposed Precambrian rock suggests that the peraluminous granite, and the Mo granite in Colorado, were derived exclusively from felsic Precambrian basement rocks and that the regional variations in the ɛNd values reflect the regional variation in the average crustal age. The Nd data confirm that the Precambrian basement underlying the NGB and eastern California is isotopically distinct from Precambrian crust in the remainder of the western United States. The similarity between the ɛNd values of peraluminous granite and Precambrian crust also suggests that the high 147Sm/144Nd (>0.13) and the low total light rare earth element (LREE) abundances characteristic of peraluminous granite in southern Arizona were imposed during the chemical evolution of the magmas. Metaluminous granite are interpreted to have formed via mixing of mantle-derived magma and large proportions of low 87Sr/86Sr (granulite facies) lower crust, except in the eastern NGB where the mantle

  15. U-Pb geochronology and Sr-Nd isotopes of Galileia and Urucum neo proterozoic granitoids suites in south-eastern Brazil; Geochronologie U-Pb et geochimie isotopique Sr-Nd des granitoides neoproterozoiques des suites Galileia et Urucum, vallee du Rio Doce, Sud-Est du Bresil

    Energy Technology Data Exchange (ETDEWEB)

    Herminio Arias Nalini Jr [Universidade Federal de Ouro Preto, Dept. de Geologia, Minas Gerais (Brazil); Herminio Arias Nalini Jr; Essaid Bilal [Ecole Nationale Superieure des Mines, Dept. de Geochimie, Centre SPIN, 42 - Saint-Etienne (France); Paquette, J.L.; Pin, Ch. [Universite Blaise Pascal, Clermont-Ferrand II, (CNRS-UMR 6525), 63 - Aubiere (France); Romulo, M. [IGG Universite de Sao Paulo (Brazil)

    2000-10-01

    U-Pb zircon and monazite dating and whole-rock Sr-Nd isotopes have been applied on Neo-Proterozoic granitoids from the Atlantic shear belt, south-eastern Brazil. U-Pb zircon results on the Galileia met-aluminous and Urucum per-aluminous suites indicate crystallisation ages of 594 {+-} 6 Ma and 582 {+-} 2 Ma respectively. Whole-rock Rb-Sr and Sm-Nd analyses on representative samples from both suites demonstrate that they mainly derive from melting of older crustal rocks. The occurrence of an old isotopic memory in the zircons from the Urucum granitoids around 2.2 Ga, in agreement with Nd model ages, suggests a Palaeo-Proterozoic age for the crustal proto-lith of these two suites, probably associated with the Transamazonico event. Owing to these new dating results and previous regional geochronological data, it can be proposed that the met-aluminous magmatism ended around 590 Ma and that the collisional peraluminous magmatism associated with the Brasiliano orogeny occurred between 584 and 570 Ma. (authors)

  16. 峡东地区闪长岩风化剖面元素和Sr-Nd同位素特征及其地球化学意义%Element and Sr-Nd isotopic geochemistry profiles of weathered dioritic rocks in the eastern Three Gorges and its implication

    Institute of Scientific and Technical Information of China (English)

    散飞雪; 凌文黎; 胡艳华; 谢淑云

    2013-01-01

    As the important period of supergene elements’ geochemistry circulation, rock weathering has important connection with the survival and the living environment of mankind. It is ideal to study the migration behaviors of elements under the surface condition in the eastern Three Gorge, located in Yichang, Hubei. This paper reports element and Sr-Nd isotopic geochemistry profiles of weathered Huangling dioritic rock mass in eastern Three Gorges. The samples were collected from three profiles, and their element mobility and Sr-Nd isotopic system stability are discussed. It demonstrates that (1) Ti is the ideal reference element for calculating element activity and indicating weathering characters; (2) CIA and CIW value increases from bedrock (D) to the top weathered layer (A);the order of major elements activity is Na, Ca>Si, P>Mg, K>Al>Fe, Mn, Ti;(3) For trace elements, Zr, Hf, Sc, V, Y and REE are relatively stable, whereas chalcophile elements Cu, Mo and Zn are varied indistinctively and Pb is enriched. Variations of Sr, Ba and Rb are different in different profiles; (4) LREE of profile 1 and 2 is relatively enriched, whereas LREE of profile 3 is relatively depleted;the rising trends ofδEu andδCe from bedrock to top weathered layers indicate preferential alteration and loss of Eu-enriched plagioclase, high oxygen fugacity resulting in transition of Ce3+ to Ce4+ and alteration and loss of soluble complex during weathering;(5) the rising trend of initial Sr isotope ratios with increasing weathering and the involvement of extra high radiogenic Sr indicates that the Rb-Sr isotope system is an open system during weathering of dioritic rocks.The decrease of initial Nd isotope ratios with increasing weathering indicates the involvement of extra low radiogenic Nd;compared with their bedrocks, the weathering layers show wider ranges ofεSr andεNd values with overall decreasing εNd. However, relatively the constant Nd isotopic model ages within error likely reflect the

  17. Accurate fast method with high chemical yield for determination of uranium isotopes ({sup 234}U, {sup 235}U, {sup 238}U) in granitic samples using alpha spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Guirguis, Laila A., E-mail: lailagurgus@yahoo.com; Farag, Nagdy M.; Salim, Adham K.

    2015-03-21

    The present study aims to use the α-spectroscopy at Nuclear Materials Authority (NMA) of Egypt. A radiochemical technique for analysis uranium isotopes was carried out for ten mineralized granitic samples together with the International standards RGU-1 (IAEA) and St{sub 4} (NMA). Several steps of sample preparation, radiochemical separation and source preparation were performed before analysis. Uranium was separated from sample matrix with 0.2 M TOPO in cyclohexane as an extracting agent with a chemical yield 98.95% then uranium was purified from lanthanides and actinides present with 0.2 M TOA in xylene as an extracting agent. The pure fraction was electrodeposited on a mirror-polished copper disc from buffer solution (NaHSO{sub 4}+H{sub 2}SO{sub 4}+NH{sub 4}OH). Rectangle pt-electrode with an anode-cathode distance of 2 cm was used. Current was 900 mA and the electrodeposition time reach up to 120 min. The achieved results show that the chemical yield ranged between 87.9±6.8 and 98±8.6. - Highlights: • Radiochemical technique for analysis uranium isotopes. • Alpha-particle spectrometry is performed after a radiochemical procedure. • Electrodeposition conditions for preparation of alpha uranium source. • Using {sup 232}U (t{sub 1/2}=70.6a, E{sub α}=5320.24 keV, intensity=69.1%) as an internal tracer makes it a highly reliable technique.

  18. Eocene Granitoids of the Okhotsk Complex in Sakhalin Island, Russian Far East: Petrogenesis and tectonic implications from zircon U-Pb ages, geochemical and Sr-Nd isotopic characteristics

    Science.gov (United States)

    Liao, Jia Ping; Alexandrov, Igor; Jahn, Bor-ming

    2016-04-01

    Sakhalin Island represents an important part of the Western Pacific Orogenic Belt (or "Nipponides"). The island comprises several accreted terrains that have recorded strike-slip displacements and block rotations from Cretaceous to Tertiary. These terrains include fore-arc basins, accretionary complexes and island arc assemblages. The stratigraphic features of most terrains can be correlated to those of Hokkaido Island of Japan. However, little research has been undertaken on the magmatic activities on Sakhalin, so a direct comparison of crustal development and tectonic activities with Hokkaido has not been fulfilled. We intend to study the petrogenesis of granitic complexes of Sakhalin to resolve this problem. In this work, we present new results of age determination and geochemical analyses of the Okhotsk Complex and discuss the tectonic implications. The Okhotsk complex is one of the three main granitoid complexes in Sakhalin Island. It intruded into the Ozersk accretionary terrain that is composed of island arc assemblages and marine sediments and has traveled northward and accreted to Sakhalin Island in Eocene. Eleven samples from the Okhotsk Complex, including 7 granitoids, 1 enclave, 2 rhyolites, and 1 dacite, were subject to zircon U-Pb dating, whole-rock geochemical and Sr-Nd isotopic analyses. The results show that the entire complex was emplaced within 42 to 44 Ma. The 7 granitoids are slightly peraluminous, ferroan, and alkali-calcic. The REE abundances of granitoids show consistent patterns with weak LREE enrichment and negative Eu anomaly. The spidergrams show negative Ta-Nb-Ti anomaly as expected in most granitoids. They possess transitional characteristics between I- and A-type granites. For isotopic signatures, the granitoids have ɛNd(t) values of +2.8 to +3.7, initial 87Sr/86Sr ratios of 0.7047 to 0.7050, and Sm-Nd model ages (TDM-1) of 700-1100 Ma. The middle Eocene magmatic episode (42-44 Ma) of the Okhotsk Complex can find its counterpart in

  19. Geochemical and Sr-Nd-Hf isotopic constraints on the origin of Late Triassic granitoids from the Qinling orogen, central China: Implications for a continental arc to continent-continent collision

    Science.gov (United States)

    Jiang, Yao-Hui; Jin, Guo-Dong; Liao, Shi-Yong; Zhou, Qing; Zhao, Peng

    2010-06-01

    The Qinling-Dabie-Sulu orogen marks the junction between the North and South China Blocks. However, the exact timing of the final coalescence of the North and South China Blocks in the Qinling orogen is poorly constrained. This paper presents new SHRIMP zircon U-Pb chronology, major and trace elements, and Sr-Nd-Hf isotope data for five early Mesozoic granitic plutons across the Qinling orogen. SHRIMP zircon U-Pb dating shows that four plutons were emplaced in the Carnian (227-218 Ma) of Late Triassic with a southward-younging trend and one pluton was emplaced in the Norian (˜ 211 Ma) of Late Triassic. The Carnian plutons consist of high-K calc-alkaline granitoids (quartz monzodiorite, quartz monzonite, granodiorite and monzogranite) and calc-alkaline diorite. These rocks are mainly metaluminous and are characterized by high Sr and low Y and Yb contents, with high Sr/Y and La/Yb ratios, and by high Mg#, higher than pure crustal melts. The Norian pluton is composed of high-K calc-alkaline two-mica granites, which are peraluminous. These granites have low Sr and high Y and Yb contents and show similar Mg# to pure crustal melts. Detailed elemental and isotopic data suggest that the Carnian plutons were emplaced in a continental arc setting coupled with the northward subduction of the Paleo-Tethyan oceanic crust. Partial melting of subducted sediments triggered by dehydration of the underlying igneous oceanic crust, with subsequent melts interacting with the overlying mantle wedge, formed the high-K calc-alkaline granitic magmas. Partial melting of the hybridized peridotitic mantle wedge induced by slab melts generated the calc-alkaline dioritic magma. The Norian pluton was emplaced during continental collision between the South Qinling terrane and South China Block, which marks the final integration of the North and South China Blocks. Partial melting of subducted sediments at a shallow depth (origin of the Norian peraluminous granites. Our new data suggest that the

  20. Geochemical and Sr-Nd-Pb Isotopic Insights of the Low-Ti basalts from Paraná-Etendeka Igneous Province, Southern Brazil: Constraints on Petrogenesis and the Role of Crustal Contamination

    Science.gov (United States)

    Raposo, I.; Barreto, C. J.; Lima, E. F. D.; Lafon, J. M.; Sommer, C. A.; Waichel, B. L.

    2015-12-01

    The south hinge of the Torres Syncline in southernmost Brazil hosts a volcanic succession of pahoehoe and rubbly Gramado-type lavas belonging to the ~132 Ma Paraná-Etendeka Igneous Province. We employ local-scale stratigraphy in three distinct profiles (Santa Cruz do Sul-Herveiras, Morro da Cruz and Lajeado geologic sections) as guidelines for geochemical and Sr-Nd-Pb isotope studies in order to discuss the petrogenesis of lava flows in a single magma type and to quantitatively evaluate the role of crustal contamination and the potential contaminants involved. In all profiles, the lava flows exhibit compositions ranging from basalt to andesite with tholeiitic affinity. The compositional and isotopic variations are not systematic according to stratigraphy, implying that the magma chamber could have undergone periodic replenishments or distinct magma pulses through time or multiple plumbling systems may have existed. The andesites (SiO2 55-58 wt.%) with ponded pahoehoe morphology represent evolved melts at early stages of volcanism with strong susceptibility to crustal contamination as they established pathways to the surface. The olivine basalts (SiO2 47-50 wt.%) and basaltic andesites (SiO2 51-56 wt.%) showing compound morphology and simple pahoehoe morphology, respectively, could be explained by longer time residence of liquids in the crust with higher degrees of crustal assimilation than the ponded pahoehoe lavas. The basaltic andesites (SiO2 52-56 wt. %) with rubbly morphology are related to late differentiation process in shallow magma chambers. Crustal assimilation process accounts for the high initial 87Sr/86Sr ratios at 0.707798-0.715751, very low ɛNd between -8.36 and -5.41, high 206Pb/204Pb ratios at 18.424-18.865, with intermediate 207Pb/204Pb and 208Pb/204Pb ratios at 15.649-15.710 and 38.618-39.369, respectively. The isotopic variations require assimilation of both Paleoproterozoic and Neoproterozoic contaminants at variable degrees.

  1. Evaluation of the effects of microscale chemical and isotopic heterogeneity of coral skeleton on conventional Sr/Ca and 18O paleothermometers

    Indian Academy of Sciences (India)

    Takehiro Mitsuguchi

    2013-10-01

    Recent studies using secondary ion mass spectrometry revealed microscale heterogeneity of Sr/Ca and 18O in shallow-water coral skeletons, i.e., Sr/Ca and 18O differ significantly between two basic microfeatures of the skeleton: the center of calcification (COC) and surrounding fibrous skeleton (SFS). The COC, in contrast with the SFS, consists of highly irregular crystals intermingled with significant amount of organic matter; therefore, analyzing the SFS only would probably be favourable for paleotemperature reconstruction. Conventional Sr/Ca and 18O paleothermometers are, however, based on the analysis of the mixture of the COC and SFS, and thus may be significantly affected by the above-mentioned heterogeneity. In this study, I have evaluated the heterogeneity-induced effects on the conventional paleothermometers of Porites skeletons using published Sr/Ca, 18O and volume-fraction data of the COC and SFS and published observations of seasonal variability of bulk skeletal density. Results indicate that the effects may yield significant or serious errors in paleotemperature reconstruction.

  2. Evaluation of the effects of microscale chemical and isotopic heterogeneity of coral skeleton on conventional Sr/Ca and O paleothermometers

    Science.gov (United States)

    Mitsuguchi, Takehiro

    2013-10-01

    Recent studies using secondary ion mass spectrometry revealed microscale heterogeneity of Sr/Ca and O in shallow-water coral skeletons, i.e., Sr/Ca and O differ significantly between two basic microfeatures of the skeleton: the center of calcification (COC) and surrounding fibrous skeleton (SFS). The COC, in contrast with the SFS, consists of highly irregular crystals intermingled with significant amount of organic matter; therefore, analyzing the SFS only would probably be favourable for paleotemperature reconstruction. Conventional Sr/Ca and O paleothermometers are, however, based on the analysis of the mixture of the COC and SFS, and thus may be significantly affected by the above-mentioned heterogeneity. In this study, I have evaluated the heterogeneity-induced effects on the conventional paleothermometers of Porites skeletons using published Sr/Ca, O and volume-fraction data of the COC and SFS and published observations of seasonal variability of bulk skeletal density. Results indicate that the effects may yield significant or serious errors in paleotemperature reconstruction.

  3. Determination on 87Sr/86Sr ratio and stratigraphic dating of single-grain foraminifera

    Institute of Scientific and Technical Information of China (English)

    TONG Jinggui; LI Shengrong; LI Xianghui; LI Qiuli; FANG Nianqiao; CHU Fengyou; CHEN Fukun

    2006-01-01

    The Sr isotopic composition of foraminifera has been used in studies of chronstratigraphy and sedimentary geochemistry. However, it is difficult to sample foraminifera without overprinting of later diagenesis, which contains enough amount of Sr for isotopic measurement. Analysis of single-grain foraminifera was successively conducted by a combination of low Sr procedural blank and high precision determination of 87Sr/86Sr ratio. This combination of single-grain foraminifera can be significant for the study and application of Sr isotopic composition of foraminifera. Measured foraminifera of this study, having a size between 250 um and 400 um, were sampled from the carbonate basement of a ferromanganese crust in western Pacific. Mean value of 87Sr/86Sr ratios of the analyzed single-grain foraminifera is 0.709150 ±0.000013 with internal precision between 4 ppm and 8 ppm for each measurement run. Average value of total procedural blank of Sr is 14 pg. It is significant but difficult to date foraminifera in carbonate basements of ferromanganese crusts. Based on the obtained value of 87Sr/86Sr ratio, the analyzed foraminifera can be dated at 0.91 +0.33/-0.39 Ma.

  4. Sulfide mineralization associated with arc magmatism in the Qilian Block, western China: zircon U-Pb age and Sr-Nd-Os-S isotope constraints from the Yulonggou and Yaqu gabbroic intrusions

    Science.gov (United States)

    Zhang, Zhao-Wei; Li, Wen-Yuan; Gao, Yong-Bao; Li, Chusi; Ripley, Edward M.; Kamo, Sandra

    2014-02-01

    The sulfide-bearing Yulonggou and Yaqu mafic intrusions are located in the southern margin of the Qilian Block, Qinghai Province, western China. They are small dike-like bodies mainly composed of gabbros and diorites. Disseminated sulfides (pyrrhotite, pentlandite, and chalcopyrite) are present as concordant lenses within the intrusions. Precise CA-ID-TIMS zircon U-Pb dating yields the crystallization ages of 443.39 ± 0.42 and 440.74 ± 0.33 Ma for the Yulonggou and Yaqu intrusions, respectively. Whole rock samples from both intrusions show light rare earth element (REE) enrichments relative to heavy REE and pronounced negative Nb-Ta anomalies relative to Th and La, which are consistent with the products of arc basaltic magmatism. The Yulonggou intrusion has negative ɛ Nd values from -5.7 to -7.7 and elevated (87Sr/86Sr) i ratios from 0.711 to 0.714. In contrast, the Yaqu intrusion has higher ɛ Nd values from -4.1 to +8.4 and lower (87Sr/86Sr) i ratios from 0.705 to 0.710. The δ34S values of sulfide separates from the Yulonggou and Yaqu deposits vary from 0.8 to 2.4 ‰ and from 2 to 4.3 ‰, respectively. The γ Os values of sulfide separates from the Yulonggou and Yaqu deposits vary between 80 and 123 and between 963 and 1,191, respectively. Higher γ Os values coupled with higher δ34S values for the Yaqu deposit relative to the Yulonggou deposit indicate that external sulfur played a bigger role in sulfide mineralization in the Yaqu intrusion than in the Yulonggou intrusion. Mixing calculations using Sr-Nd isotope data show that contamination with siliceous crustal materials is more pronounced in the Yulonggou intrusion (up to 20 wt%) than in the Yaqu intrusion (market condition due to small sizes and low Ni grades, which can be explained by late-stage sulfide saturation after extensive olivine fractional crystallization from the magmas. Based on these observations, we suggest a shift of focus for Ni exploration in the region from mafic/gabbroic intrusions

  5. Abrupt Change Analyses of Oxygen, Carbon Isotope Values and Sr Contents in a Stalagmite Retrieved from Songjia Cave, NE Sichuan%大滁城人居环境适宜性研究

    Institute of Scientific and Technical Information of China (English)

    李军利; 徐松南; 李建梅; 潘静

    2012-01-01

    以1km×1km栅格为基本单元,选取交通路网指数、水域指数、学校指数、居住影响力指数与地被指数等影响因子,运用GIS技术建立大滁城人居环境指数模型,定量研究大滁城规划区人居环境的适宜程度及其空间规律性。结果表明:大滁城人居环境指数呈现由中心区域向周边地区递减的趋势;人居环境指数与人口密度有较好的相关性,二者的一次拟合度R2=0.8361。一般适宜以上的地区132km2,接近大滁城面积的2.96%,相应的人口占大滁城8.75%,其中3.3%的人口聚集在0.78%人居环境高度适宜和比较适宜地区;临界适宜地区698km2,占大滁城面积的15.69%,人口39.33万;适宜性相对较差的地区3619km2,人口108.91万,占大滁城总面积的81.35%。%We analyze the abrupt changes of oxygen, carbon isotope values and Sr contents in stalagmite S J3 retrieved from Song:jia Cave, Central China. Some conclusions are given below : ( 1 ) Oxygen isotope values record the transition from Last Glacial Maximum to Heinrich Event One period;(2) Carbon isotope values record the transition from H1 cold period to BoilingAllerod warm period ; ( 3 ) The correlation between Carbon isotope values and Sr contents indicate that the local East Asian summer monsoon were in - phase with the winter monsoon during 19.8 - 15.3ka while out of phase during 15.3 - 14.8ka. It' s obvious that stalagmite S J3 records the palaeoclimate changes between colddry and warm wet conditions while different climate proxies were dissimilar in sensitivities with regard to climate changes.

  6. Rapid Environmental Fluctuations Recorded over the Last Glacial/Interglacial Cycle in the Sediments from Borehole PRGL1-4 (Gulf of Lions; Western Mediterranean) using Radiogenic Isotopes (Sr & Nd)

    Science.gov (United States)

    Nizou, J.

    2015-12-01

    The study of sediments deposited and preserved in oceanic basins unable us to examine how terrigenous sediment supply varied through time in relation to paleoenvironmental and climatic changes on land. The geochemical and isotopic compositions of marine sediment are used to unravel its provenance, and provide information about its formation. Providing that the paleoclimatic frame is known, such data give an insight into the rock-source location and allow us to decipher between genetic processes of mechanical erosion and chemical alteration. Borehole PRGL1-4 (European project PROMESS), located in the Gulf of Lions (W Mediterranean) at 300 mwd, was investigated geochemically at high-temporal resolution over the last glacial/interglacial cycle (i.e. 130 ka) to study sediment-source variations during rapid climate changes. Besides, sediments originating from the Rhône's and the Pyreneo-Languedocian's catchment areas have been analyzed to measure the isotopic composition of five source end-members that are the Alps, the Higher Rhône valley, the Lower Rhône valley, the Languedoc and the Pyrenees. Epsilon Nd and 87Sr/86Sr were measured on 60 samples encompassing 4 marine isotopic stages with an emphasis on Heinrich events. The epsilon Nd values of PRGL1-4 lean towards the Lower Rhône valley unradiogenic end-member during cold stadial intervals, and towards the Alpine radiogenic end-member during warm interstadials. The presence of an ice cap over the crystalline Alpine watershed during cold phases could prevent the sediments originating from this region from reaching the Gulf of Lions. The same pattern is observed during the time of Heinrich events. An influence of the sea level variations on the sedimentation at the borehole site during the Heinrich events is unlikely since they are only 10 to 15 m in amplitude. Furthermore, a major isotopic shift in epsilon Nd mean values is displayed around 40 ka that coincides with the connection of the Durance to the Rhône River

  7. 87Sr/86Sr-ratios and Sr-contents of deep ground waters, minerals and rocks from the crystalline and the Trias of Northern Switzerland

    International Nuclear Information System (INIS)

    In order to determine the origin of groundwaters and their interaction with the host rock, the amount and ratio of strontium isotopes in groundwaters, vein minerals, authigenic cements and whole rocks were measured in the crystalline basement and Triassic sediments of northern Switzerland. The groundwaters in the fractured basement aquifer generally show Sr-isotope ratios that range between 0.716 and 0.718. These ratios in the groundwaters are mainly determined by reaction with Sr-rich minerals that were formed during a Permian hydrothermal event. With minor exceptions, the Sr-isotope ratios of most vein minerals are not in equilibrium with those of the present groundwaters. The waters of the Buntsandstein aquifer are characterized by slightly lower Sr-isotope ratios and a higher Sr-content than in the corresponding basement aquifer waters. Buntsandstein waters are considered to have evolved from the waters of the basement aquifer through dissolution of calcite and sulphate present in the Buntsandstein. Although the Sr-isotope ratios in Buntsandstein vein minerals and waters are similar the relative amount of Sr (assuming equilibrium partitioning) suggests these vein minerals did not precipitate from the present waters. The much lower Sr-isotope ratio characteristic of waters in the Muschelkalk aquifer (0.708 to 0.709) readily distinguishes these from the Buntsandstein and basement waters. The low Sr-isotope ratios in the Muschelkalk waters are, however, higher than those measured from marine sulphates in the Muschelkalk, and may result from dissolution of dolomite and continental sulphates. Measured variations in the Sr-isotope ratios of successive authigenic minerals indicate that the Sr-isotope composition in the groundwaters fluctuated through geological time. (author) 32 refs., 4 figs., 1 tab

  8. Molar-tooth Carbonate Sequences and Sr Isotopes in the Neoproterozoic for Stratigraphic Correlation:Research in the Jilin-Liaoning-Xuzhou-Huaiyang Area of the Sino-Korean Plate and Its Correlation with the Yangtze Plate

    Institute of Scientific and Technical Information of China (English)

    MENG Xianghua; GE Ming; LIU Yanxue; KUANG Hongwei; LIU Weifu; Francoise G. BOURROUILH-LE JAN; Robert BOURROUILH

    2004-01-01

    Based on a study of Neoproterozoic carbonates in the Jilin-Liaoning-Xuzhou-Huaiyang area, especially its cyclic sequence stratigraphy and Sr isotopes, two maximum sea flooding events (at 820 Ma and 835 Ma) have been identified. The resulting isochronous stratigraphic correlation proves that these Precambrian strata were connected between the Qingbaikou and the Nanhuan systems with a time range from 750 Ma to 850 Ma. The disappearance of microsparite carbonate and coming of a glacial stage offer important evidence for worldwide stratigraphic correlation and open a window for further correlation of the stratigraphic successions across the Sino-Korean and Yangtze Plates. A new correlation scheme is therefore provided based on our work.

  9. Contrasted crustal sources as defined by whole-rock and Sr-Nd-Pb isotope geochemistry of neoproterozoic early post-collisional granitic magmatism within the Southern Brazilian Shear Belt, Camboriú, Brazil

    Science.gov (United States)

    Florisbal, Luana Moreira; de Assis Janasi, Valdecir; de Fátima Bitencourt, Maria; Stoll Nardi, Lauro Valentim; Heaman, Larry M.

    2012-11-01

    The early phase of post-collisional granitic magmatism in the Camboriú region, south Brazil, is represented by the porphyritic biotite ± hornblende Rio Pequeno Granite (RPG; 630-620 Ma) and the younger (˜610 Ma), equigranular, biotite ± muscovite Serra dos Macacos Granite (SMG). The two granite types share some geochemical characteristics, but the more felsic SMG constitutes a distinctive group not related to RPG by simple fractionation processes, as indicated by its lower FeOt, TiO2, K2O/Na2O and higher Zr Al2O3, Na2O, Ba and Sr when compared to RPG of similar SiO2 range. Sr-Nd-Pb isotopes require different sources. The SMG derives from old crustal sources, possibly related to the Paleoproterozoic protoliths of the Camboriú Complex, as indicated by strongly negative ɛNdt (-23 to -24) and unradiogenic Pb (e.g., 206Pb/204Pb = 16.0-16.3; 207Pb/204Pb = 15.3-15.4) and confirmed by previous LA-MC-ICPMS data showing dominant zircon inheritance of Archean to Paleoproterozoic age. In contrast, the RPG shows less negative ɛNdt (-12 to -15) and a distinctive zircon inheritance pattern with no traces of post-1.6 Ga sources. This is indicative of younger sources whose significance in the regional context is still unclear; some contribution of mantle-derived magmas is indicated by coeval mafic dykes and may account for some of the geochemical and isotopic characteristics of the least differentiated varieties of the RPG. The transcurrent tectonics seems to have played an essential role in the generation of mantle-derived magmas despite their emplacement within a low-strain zone. It may have facilitated their interaction with crustal melts which seem to be to a large extent the products of reworking of Paleoproterozoic orthogneisses from the Camboriú Complex.

  10. Origin of the granites and related Sn and Pb-Zn polymetallic ore deposits in the Pengshan district, Jiangxi Province, South China: constraints from geochronology, geochemistry, mineral chemistry, and Sr-Nd-Hf-Pb-S isotopes

    Science.gov (United States)

    Xu, Bin; Jiang, Shao-Yong; Luo, Lan; Zhao, Kui-Dong; Ma, Liang

    2016-05-01

    The Pengshan Sn and Pb-Zn polymetallic deposits are located in the south margin of the Jiujiang-Ruichang (Jiurui) district of the Middle-Lower Yangtze River Metallogenic Belt in South China. Four large deposits include Huangjinwa, Zengjialong, Jianfengpo, and Zhangshiba, the former three are Sn-dominant deposits which occur as stratiform orebodies in the contact zones of the Pengshan granites and within the country rock strata, whereas Zhangshiba consists of stratiform Pb-Zn orebodies within the Precambrian metasedimentary strata. In this study, we present results on zircon U-Pb ages, major and trace elements, and mineral chemistry as well as Sr-Nd-Hf isotope data of the granites, Pb and S isotopes of both the Sn-dominant and Pb-Zn dominant deposits, and U-Pb dating of cassiterite from the Pengshan district. SHRIMP and LA-ICP-MS zircon U-Pb dating shows that the Pengshan granites were emplaced in the Early Cretaceous (129-128 Ma), which is in good agreement with the U-Pb dating (130-128 Ma) of cassiterite from the Jianfengpo Sn deposit. The Pengshan granites consist mainly of weakly peraluminous highly fractionated I-type affinity granitic rocks. Detailed elemental and isotopic data suggest that the granites formed by partial melting of Mesoproterozoic metamorphic basement materials with minor input of mantle-derived melts. The mineral chemistry of biotite demonstrates that the Pengshan granitic magma had a low oxygen fugacity, thereby precluding the tin dominantly partitioning into the rock-forming silicate minerals and favoring accumulation in the exsolved residual liquid during magma crystallization stages. Sulfur isotopes show a relatively heavy sulfur isotopic composition from 5.8 to 17.6 ‰, and no difference for sulfur isotopes between the Sn deposits (5.8-13.4 ‰, Huangjinwa, Zengjialong, Jianfengpo) and the Pb-Zn deposit (mostly 7.1-13.0 ‰, except for one 17.6 ‰, Zhangshiba). The sulfur isotope data of pyrite from the host sedimentary rocks show

  11. Overview of the geochemistry and Rb/Sr, Sm/Nd isotopes of Middle Jurassic and Tertiary granitoid intrusions: a new insight on tectono-magmatism and mineralization of this period in Iran

    Directory of Open Access Journals (Sweden)

    Mohammad Ali Jazi

    2012-10-01

    Full Text Available One of the most intensive occurrences of magmatism in Iran was in the middle Jurassic period. Among the granitoid intrusions in this period as discrete bodies or complexes can be pointed to Aligoodarz, Alvand, Astaneh, Boroujerd, Malayer, and Chah-Dozdan in the Sanandaj-Sirjan zone; Shir-kuh and Ayrakan in the Central Iran zone; Shah-kuh, Sorkh-kuh and Kalateh-Ahani in the Lut Block. These granitoids are mostly peraluminous and belong to high-K calc-alkaline series. CaO/Na2O ratios (0.12 to 8.37 mostly suggest a clay-free source for formation of the intrusive rocks magma. Chondrite-normalized Rare Earth Elements (REEs diagram do not display high enrichment of Light Rare Earth Elements (LREEs than Heavy Rare Earth Elements (HREEs and general pattern is relatively flat. In addition, diagram shows Eu negative anomaly, which can be attributed to indicate reducing conditions in formation of magma and/or magma derived from plagioclase depth as source. The lower continental crust-normalized spider diagram indicates enrichment in LILE (Rb, Cs, and K and LREE (La and Ce and depletion in Ba, Nb, Ta, Sr, and Ti. Initial 87Sr/86Sr ratios are 0.70609 to 0.71938 and initial εNd values are negative (from -6.51 to -1.1 indicating that magma derived from continental crust. Geochemical and isotopic evidence of the intrusive rocks shows continental crust origin (S-type granitoid and due to continental collision. Geological findings such as stop in sedimentation, regional metamorphism, ophiolite displacement, and continental collision-related mineralization confirm continental collision between Iranian and Arabian plates in the Middle Jurassic period.

  12. Emplacement ages, geochemical and Sr-Nd-Hf isotopic characterization of Mesozoic to early Cenozoic granitoids of the Sikhote-Alin Orogenic Belt, Russian Far East: Crustal growth and regional tectonic evolution

    Science.gov (United States)

    Jahn, Bor-ming; Valui, Galina; Kruk, Nikolai; Gonevchuk, V.; Usuki, Masako; Wu, Jeremy T. J.

    2015-11-01

    The Sikhote-Alin Range of the Russian Far East is an important accretionary orogen of the Western Pacific Orogenic Belt. In order to study the formation and tectonic evolution of the orogen, we performed zircon U-Pb dating, as well as geochemical and Sr-Nd-Hf isotopic analyses on 24 granitoid samples from various massifs in the Primorye and Khabarovsk regions. The zircon dating revealed that the granitoids were emplaced from 131 to 56 Ma (Cretaceous to Paleogene). In the Primorye Region, granitoids in the coastal Sikhote-Alin intruded the Cretaceous Taukha Accretionary Terrane from ca. 90 to 56 Ma, whereas those along the Central Sikhote-Alin Fault zone intruded the Jurassic Samarka Accretionary Terrane during ca. 110-75 Ma. The "oldest" monzogranite (131 Ma) was emplaced in the Lermontovka area of the NW Primorye Region. Granitoid massifs along the Central Sikhote-Alin Fault zone in the Khabarovsk Region formed from 109 to 58 Ma. Thus, the most important tectonothermal events in the Sikhote-Alin orogen took place in the Cretaceous. Geochemical analysis indicates that most samples are I-type granitoids. They have initial 87Sr/86Sr ratios ranging from 0.7040 to 0.7083, and initial Nd isotopic ratios, expressed as εNd(t) values, from +3.0 to -5.0 (mostly 0 to -5). The data suggest that the granitoid magmas were generated by partial melting of sources with mixed lithologies, including the subducted accretionary complex ± hidden Paleozoic-Proterozoic basement rocks. Based on whole-rock Nd isotopic data, we estimated variable proportions (36-77%) of juvenile component (=mantle-derived basaltic rocks) in the generation of the granitic magmas. Furthermore, zircon Hf isotopic data (εHf(t) = 0 to +15) indicate that the zircon grains crystallized from melts of mixed sources and that crustal assimilation occurred during magmatic differentiation. The quasi-continuous magmatism in the Sikhote-Alin orogen suggests that the Paleo-Pacific plate subduction was very active in the

  13. The Rb-Sr system

    International Nuclear Information System (INIS)

    This manual is intended to serve as a guide to the chemical procedures involved in Rb-Sr isotopic analysis as conducted at the Institute of Nuclear Sciences. Included are notes on the experimental developments made over the last 2.5 years, especially those involving rock dissolution and cation exchange chromatography

  14. Isotopic characteristics (Nd and Sr) of the intrusive plutonism at the northwestern Amazonian Craton, Venezuela, and implications for the Paleoproterozoic evolution; Caracteristicas isotopicas (Nd e Sr) do plutonismo intrusivo no extremo NW do Craton Amazonico, Venezuela, e implicacoes para a evolucao paleoproterozoica

    Energy Technology Data Exchange (ETDEWEB)

    Teixeira, Wilson; Tassinari, Colombro Celso G. [Sao Paulo Univ., SP (Brazil). Inst. de Geociencias. Dept. de Mineralogia e Geotectonica; Mondin, M. [Sao Paulo Univ., SP (Brazil). Inst. de Geociencias. Programa de Pos-graduacao em Recursos Minerais e Hidrogeologia

    2002-12-15

    Nd and Sr analyses were performed on selected granitoid plutons that intrude Archean and Paleoproterozoic domains of the Guyana shield (Venezuela). The isotopic signatures of these plutons together with the geochronologic background of the country rocks are used to constrain their magma genesis and tectonic setting within the Paleoproterozoic evolutions of mobile belts (Maroni-Itacaiunas and Ventuari-Tapajos provinces) of the Amazonian Craton. The Encrucijada Suite (2187 +- 94 Ma), which intrudes Archean rocks of the Imataca Complex, originated predominantly from partial melt of this crust, as supported by negative epsilon{sub Nd(2.1Ga)} values (-2.2 to - 4.9) and T{sub DM} ages between 2.82 and 2.49 Ga. Conversely, the plutons from the Supamo Complex (2230 - 2050 Ma) and Cuchivero Group (1980 - 1830 Ma), occurring within the adjoining Paleoproterozoic provinces, are juvenile in nature (derived from roughly contemporary protoliths). These bodies display T{sub DM} ages between 2.13 and 2.22 Ga, as well as positive epsilon{sub Nd(2.1Ga)} values (+0.74 to + 3.05). Isotopic correlation diagrams (143 Nd/144 Nd vs. 147 Sm/144 Nd and 143 Nd/144 Nd vs. time) plotted together with the plutonic rocks and Imataca Complex rocks were evaluated taking into account the geologic background of the NW part of the Amazonian Craton. Interpretation of these isotopic data supports the idea of tectonic juxtaposition between the Imataca Complex and the Maroni-Itacaiunas province during the Transamazonian orogeny (2.25 - 2.05 Ga). On the other hand, the Cuchivero Group plutons have a contrasting isotopic signature compared to the other Paleoproterozoic plutonic rocks. This is consistent with the existence of a tectonic boundary between the Maroni-Itacaiunas and the Ventuari-Tapajos province in the late Paleoproterozoic. (author)

  15. High-precision 87Sr/86Sr analyses in wines and their use as a geological fingerprint for tracing geographic provenance.

    Science.gov (United States)

    Marchionni, Sara; Braschi, Eleonora; Tommasini, Simone; Bollati, Andrea; Cifelli, Francesca; Mulinacci, Nadia; Mattei, Massimo; Conticelli, Sandro

    2013-07-17

    The radiogenic isotopic compositions of inorganic heavy elements such as Sr, Nd, and Pb of the food chain may constitute a reliable geographic fingerprint, their isotopic ratios being inherited by the geological substratum of the territory of production. The Sr isotope composition of geomaterials (i.e., rocks and soils) is largely variable, and it depends upon the age of the rocks and their nature (e.g., genesis, composition). In this study we developed a high-precision analytical procedure for determining Sr isotopes in wines at comparable uncertainty levels of geological data. With the aim of verifying the possibility of using Sr isotope in wine as a reliable tracer for geographic provenance, we performed Sr isotope analyses of 45 bottled wines from four different geographical localities of the Italian peninsula. Their Sr isotope composition has been compared with that of rocks from the substrata (i.e., rocks) of their vineyards. In addition wines from the same winemaker but different vintage years have been analyzed to verify the constancy with time of the (87)Sr/(86)Sr. Sr isotope compositions have been determined by solid source thermal ionization mass spectrometry following purification of Sr in a clean laboratory. (87)Sr/(86)Sr of the analyzed wines is correlated with the isotopic values of the geological substratum of the vineyards, showing little or no variation within the same vineyard and among different vintages. Large (87)Sr/(86)Sr variation is observed among wines from the different geographical areas, reinforcing the link with the geological substratum of the production territory. This makes Sr isotopes a robust geochemical tool for tracing the geographic authenticity and provenance of wine.

  16. Petrology, 40Ar/39Ar age, Sr-Nd isotope systematics, and geodynamic significance of an ultrapotassic (lamproitic) dyke with affinities to kamafugite from the easternmost margin of the Bastar Craton, India

    Science.gov (United States)

    Rao, N. V. Chalapathi; Atiullah; Burgess, R.; Nanda, Purnendu; Choudhary, A. K.; Sahoo, Samarendra; Lehmann, B.; Chahong, Ngazipmi

    2016-04-01

    We report the mineralogy, bulk-rock geochemistry, 40Ar/39Ar (whole-rock) age and radiogenic (Sr and Nd) isotope composition of an ultrapotassic dyke from Sakri (Nuapada lamproite field) located at the tectonic contact between the easternmost margin of the Bastar craton and Eastern Ghats Mobile Belt, India. The Sakri dyke has a mineralogy which strongly resembles a lamproite sensu stricto (viz.,Ti-rich phlogopite, Na-poor diopside, Fe-rich sanidine, ulvospinel trend and Sr-rich apatite). However, its bulk-rock major element geochemical characteristics (viz., extreme silica-undersaturated nature) resemble sensu lato kamafugite from Toro Ankole, Uganda, East African Rift, and Alto Paranaiba Province, Brazil. The Sakri dyke also displays certain compositional peculiarities (viz., high degree of evolution of mica composition from phlogopite to biotite, elevated titanium and aluminum in clinopyroxene and significantly lower bulk Mg#) when compared to the ultrapotassic rocks from various Indian cratons. 40Ar/39Ar dating gave a plateau age of 1045 ± 9 Ma which is broadly similar to that of other Mesoproterozoic (i) lamproites from the Bastar and Bundelkhand cratons, and (ii) kimberlites from the Eastern Dharwar craton. Initial bulk-rock Sr (0.705865-0.709024) and Nd (0.511063-0.511154) isotopic ratios reveal involvement of an `enriched' source region with long-term incompatible element enrichment and a depleted mantle (TDM) Nd model age of 2.56 Ga straddling the Archaean-Proterozoic chronostratigraphic boundary. The bulk-rock incompatible trace element ratios (Ta/Yb, Th/Yb, Rb/Ba and Ce/Y) of the Sakri ultrapotassic dyke negate any significant influence of crustal contamination. Small-degree melting (1 to 1.5 %) of a mixed garnet-facies and spinel-facies phlogopite lherzolite can account for its observed REE concentrations. Whereas the emplacement of the Sakri ultrapotassic dyke is related to the amalgamation of the supercontinent of Rodinia, its overlapping geochemical

  17. U-Pb Dating, whole rock and Sr-Nd-Pb-O isotope geochemistry of collisional magmatism in the CACC: Çiçekdaǧ igneous complex (ÇIC)

    Science.gov (United States)

    Deniz, Kiymet; Kagan Kadioglu, Yusuf; Stuart, Finlay; Ellam, Rob; Boyce, Adrian; Condon, Daniel

    2015-04-01

    The closure of Neotethys induced from calcalkaline through alkaline magmatism within the Central Anatolia Crystalline Complex (CACC) during the late Cretaceous-early Paleogene. Timing of these magmatism is very important for understanding the magmato-tectonic evolution and the relation with the collision. Despite the genesis of felsic products are well understood, there is lack of petrogenetic explanation about especially alkaline mafic products. The relation between Neotethyan ophiolites and late alkaline dykes which haven't reported before is the most important undeclared gap. Çiçekdağ igneous complex (ÇIC) is one of the best area for explaining all of these problems within the CACC. In accordance with these purposes, we have carried out detailed petrographic, whole rock geochemical, Sr-Nd-Pb-O isotopic and geochronological (U/Pb and Ar/Ar) study of the rocks in the ÇIC in order to unravel the magmatic history of the CACC and thus constrain the tectonic history. The intrusive rocks of the ÇIC are differentiated into four main group as an ophiolites, calcalkaline series, alkaline series and late alkaline dykes. The felsic and mafic units intruded to the ophiolitic rocks. The calcalkaline series mostly composed of monzonites and monzodiorite porphyry whereas the alkaline series consist of syenites and feldspathoid-bearing gabbros. Variations in the major oxide compositions of both rock series can be attributed with fractionation of clinopyroxene, plagioclase, amphibole, apatite and iron titan oxide minerals. The high 87Sr/86Sr and low 143Nd/144Nd of both series are indicative of mantle sources with large continental crustal components. Feldspar and quartz oxygen isotope data from calcalkaline and alkaline series have a range of δ18O values 5.1-11.4o 8.3-9.2o and 7.7-14.1o 10.2-13.7o respectively and are compatible with the values for I-A-type granitoids. Both rock series represent the mixed (mantle-crustal) origin. The combination of all data suggest that

  18. Geochemical and Nd-Sr-Pb-O isotopic constrains on Permo-Triassic magmatism in eastern Qaidam Basin, northern Qinghai-Tibetan plateau: Implications for the evolution of the Paleo-Tethys

    Science.gov (United States)

    Chen, Xuanhua; Gehrels, George; Yin, An; Zhou, Qi; Huang, Penghui

    2015-12-01

    Eastern Qaidam Basin of the northern Qinghai-Tibetan plateau is located in a transitional zone between the Permo-Triassic Paleo-Tethyan orogenic belt in the south and the early Paleozoic Qilian orogenic belt in the north. Here we present geochemical and Sr-Nd-Pb-O isotopic data for the Permo-Triassic plutons in eastern Qaidam Basin. Bulk-rock geochemical data and regional geological studies indicate that these plutons consist mainly of subduction-related high-K calc-alkaline metaluminous, I-type granitoids, which occurred during the northward subduction of the Paleo-Tethyan oceanic lithosphere below the southern continental margin of the Kunlun-Qaidam terrane. The εNd(t) values of these Permo-Triassic granitoids are between -9.4 and -3.0, and εSr(t) values are from -20.33 to +168.20. Nd isotopic compositions indicate that the granitoids can come from a pre-existed materials formerly originated from an enriched mantle (EM II) source. The TDM2 model ages of 1.28-1.78 Ga implies that the arc-induced Triassic granitoids were derived melts of Meso-Proterozoic basement rocks of the Kunlun-Qaidam terrane that is bounded by the early Paleozoic Qilian suture zone to the north and the Triassic Kunlun suture zone in the south. The Permo-Triassic granitoids yield initial ratios of 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb values from 18.295 to 19.096, 15.617 to 15.692, and 37.960 to 38.531, respectively. The Pb isotope composition of the granitoids is very similar to that of the Mesozoic granitoids from the western segment of the east of the study area. Geochemical analyses of the plutons, integrated with previous LA ICP-MS U-Pb zircon dating, reveal two series of Permo-Triassic arc magmatisms in eastern Qaidam Basin. Both the series of magmatism display reversed trends with the classic Bowen's reaction series. The new geochemical evidence suggest that the arc magmatism in eastern Qaidam Basin was induced by fluid-fluxing melting of an enriched lithospheric mantle and rock

  19. Zircon LA-ICP MS U-Pb Age, Sr-Nd-Pb Isotopic Compositions and Geochemistry of the Triassic Post-collisional Wulong Adakitic Granodiorite in the South Qinling, Central China, and Its Petrogenesis

    Institute of Scientific and Technical Information of China (English)

    QIN Jiangfeng; LAI Shaocong; WANG Juan; LI Yongfei

    2008-01-01

    The Indosinian post-collisional Wulong pluton intruded into the Mesoproterozoic Fuping Group, South Qinling, central China. In the southern part of the pluton, some mafic enclaves have sharp or gradational contact relationships with the host biotite granodiorite. Geochemistry, zircon LA-ICP MS (laser ablation inductively-coupled plasma mass spectrometry) U-Pb chronology and Sr- Nd-Pb isotope geochemistry of the pluton are reported in this paper. The biotite granodiorite shows close compositional similarities to high-silica adakite. Its chondrite-normalized REE patterns are characterized by strong HREE depletion (Yb = 0.33-0.96 10-6 and Y = 4.77-11.19×10-6), enrichment of Ba (775-1386×10-6) and Sr (643-1115×10-6) and high Sr/Y (57.83-159.99) and Y/Yb (10.99-14.32) ratios, as well as insignificant Eu anomalies (δEu = 0.70-0.83), suggesting a feldspar-poor, garnet±amphibole-rich residual mineral assemblage. The mafic enclaves have higher MgO (4.15- 8.13%), Cr (14.79-371.31×10-6), Ni (20.00-224.24×10-6) and Nb/Ta (15.42-21.91) than the host granodiorite, implying that they are mantle-derived and might represent underplated mafic magma. Zircon LA-ICP MS dating of the granodiorite yields a 20.6Pb/238U weighted mean age of 208±2 Ma (MSWD=0.50, 1σ), which is the age of emplacement of the host biotite granodiorite. This age indicates that the Wulong pluton formed during the late-orogenic or post-collisional stage (≤242±21 Ma) of the South Qinling belt. The host biotite granodiorite displays 87Sr/86Sr = 0.7059-0.7062, Isr = 0.7044-0.7050,143Nd/144Nd = 0.51236-0.51238, εNd(t)=-2.26 to-2.66,2.6Pb/2.4pb=18.099-18.209,207Pb/2.4pb=15.873-15.979 and 2.8Pb/204pb=38.973-39.430. Those ratios are similar to those of the Mesoproterozoic Yaolinghe Group in the South Qinling. Furthermore, its Nd isotopic model age(~1.02 Ga) is consistent with the age (~1.1 Ga) of the Yaolinghe Group. Based on the integrated geological and geochemical studies, coupled with previous

  20. A theoretical study of soft mode behavior and ferroelectric phase transition in 18O-isotope exchanged SrTiO3: evidence of phase coexistence at the quantum critical point

    Science.gov (United States)

    Mkam Tchouobiap, S. E.

    2014-02-01

    Motivated by recent experiments, the dynamics of the ferroelectric soft mode and the ferroelectric phase transition mechanism in 18O isotope exchanged systems SrTi(16O1-x18Ox)3 (abbreviated as STO18-x) are reinvestigated as a function of the 18O isotope exchange rate x, within a quasiharmonic model (QHM) for quantum ferroelectric modes in double-Morse local potential with mean-field approximation interactions between modes. The approach was realized within the framework of the variational principle method at finite temperature through the quantum mean-field approximation and by taking into account the effect of isotope replacement through the predominant mass effect, the cell volume effect, homogeneity of the composition throughout the material and the concentration-dependent ferroelectric mode distortion effect. The dynamics of the lowest-frequency soft phonon mode clearly presents an increased softening phenomenon with increasing x and a complete one at the corresponding phase transition temperature Tc, demonstrating the perfect soft-mode-type quantum ferroelectric phase transition for x ⩾ xc. Also, a ferroelectric-paraelectric phase coexistence state has been found near the quantum critical point xc and its origin is discussed. The ferroelectric phase transition mechanism is analyzed and its nature discussed, where a second-order phase transition close to the tricritical point is predicted. In addition, the effect of quantum fluctuations on the soft mode dynamics is discussed which reveals its reduction with increasing x and the crossover of the soft mode dynamics from the quantum to the classic one at the full 18O exchange limit x = 1, for which the origin seems to lie in the new homogeneity associated with the direct reduction of quantum fluctuations effects on the soft mode behavior. Within the QHM, consistent agreement with some of the previous experimental results and theoretical predictions of quantum ferroelectricity throughout the full range of x are

  1. Distribution of Natural Radioactivity, 137Cs, 90Sr, and Plutonium Isotopes in a Water Column and Sediment Core along the Algerian Coast

    OpenAIRE

    Noureddine, A; M. BENKRID; R. Maoui; Menacer, M.; R. BOUDJENOUN

    2007-01-01

    Concentrations of natural (40K, 210Pb, uranium, and thorium series) and artificial radioelements (137Cs, 90Sr, 239+240Pu) were determined in seawater and sediment samples collected from stations along the Algerian coast. Seawater was collected from the surface to a maximum depth of 2000 m; the sediment cores were sampled from a depth of around 1500 m. This work was carried out in August 2001, in the framework of the Regional African project /7/004 (RAF), by the accomplishment of an oceanogra...

  2. 87Sr/86Sr measurements on marine sediments by inductively coupled plasma-mass spectrometry

    International Nuclear Information System (INIS)

    The application of inductively coupled plasma-mass spectrometry (ICP-MS) is documented for the study of the strontium isotopic composition (87Sr/86Sr) in geological samples, i.e. in the marine lithic fraction of core sediments. Methods for the determination of the isotopic composition, its accuracy and precision are reported. The results obtained simultaneously on 11 samples by both ICP-MS and thermal ionization mass spectrometry (TIMS) reveal a very good correlation (r2 = 0.955). (orig.)

  3. 蒙西斑岩铜钼矿含矿岩体地球化学和Sr-Nd-Pb同位素特征%Geochemical and Sr-Nd-Pb Isotopic Characteristics of the Ore-bearing Rock in Mengxi Porphyry Cu-Mo Deposit

    Institute of Scientific and Technical Information of China (English)

    刘建朝; 王瑞美; 程建新; 彭素霞; 张海东; 王得权; 郑利宏

    2014-01-01

    Ore-bearing porphyry in Mengxi porphyry Copper-Molybdenum deposit is plagiogranite porphyry.The geo-chemical and Sr-Nd-Pb isotope research of porphyry bodies show that rocks are peraluminous calc-alkaline,enriched in large-ion lithophile elements Rb,Ba,U,K,Pb,Sr and depleted in high field strength elements Th,Ta,Nb,Nd,Ti.Through the studies on porphyry bodies,it is identified for rock bodies characterized with low (87Sr/86Sr) ⅰ ratio (0.7046 5~0.7053 7) and high εNd(t) value (-2.2~6.6).(206Pb/204Pb)i ratio of the rock bodies range from 17.13 to 17.33,(207Pb/204Pb)i ratio from 15.47 to 15.54,and (208Pb/204Pb)i ratio from 37.11 to 37.33.These characteristics indicate that the porphyry bodies possibly formed in arc environment, and the magmatic materials were derived from the mantle,involved some portions of crustal rocks,which may related with partial melting of subducted oceanic crust.Qiongheba in eastern Junggar is a potential area for prospecting the phyry Cu deposit.%蒙西斑岩铜钼矿含矿斑岩体主要为斜长花岗斑岩。通过对含矿斑岩体地球化学和Sr-Nd-Pb同位素特征的研究,确立斑岩体为过铝质钙碱性系列岩石,富集Rb,Ba,U,K,Pb,Sr等大离子亲石元素,亏损Th,Ta,Nb,Nd,Ti等高场强元素;具低的(87Sr/86Sr)ⅰ值(0.70465~0.70537)和相对较高的εNd(t)值(-2.2~6.6),且有较低的初始铅同位素比值(206Pb/204Pb)i=17.13~17.33,(207Pb/204Pb)i=15.47~15.54,(208Pb/204Pb)i=37.11~37.33。上述特征表明其形成于岛弧环境,岩浆物质来源以幔源为主,但也有少量壳源组分参与,岩浆的形成可能与洋壳的俯冲作用有关。东准噶尔琼河坝地区是形成和寻找斑岩型铜矿的有利地区。

  4. Chemical, multi-isotopic (Li-B-Sr-U-H-O) and thermal characterization of Triassic formation waters from the Paris Basin

    OpenAIRE

    Millot, Romain; Guerrot, Catherine; Innocent, Christophe; Négrel, Philippe; Sanjuan, Bernard

    2011-01-01

    International audience This work reports chemical and isotope data and temperature estimates for seven water samples collected from Triassic formations in the Paris Basin in France. Four samples were collected in the central part of the Basin (saline waters) and three were collected at the edge of the Basin near the recharge zone (dilute waters). The saline waters collected from the Chaunoy and Champotran boreholes have high salinities (around 120 g/L) and very similar chemical and isotopi...

  5. The Aguablanca Cu–Ni ore deposit (Extremadura, Spain), a case of synorogenic orthomagmatic mineralization: age and isotope composition of magmas (Sr, Nd) and ore (S)

    OpenAIRE

    Casquet, César; Galindo Francisco, Mª del Carmen; Tornos Arroyo, Fernando; Velasco Roldán, Francisco; Canales Gallarosa, Ángel

    2001-01-01

    The Aguablanca Cu–Ni orthomagmatic ore deposit is hosted by mafic and ultramafic rocks of the Aguablanca stock, which is part of the larger, high-K calc-alkaline Santa Olalla plutonic complex. This intrusive complex, ca. 338 Ma in age, is located in the Ossa-Morena Zone (OMZ) of the Iberian Variscan Belt. Mineralization consists mainly of pyrrhotite, pentlandite and chalcopyrite resulting from the crystallization of an immiscible sulphide-rich liquid. Isotope work on the host igne...

  6. Sr and O isotopic characteristics of porphyries in the Qinling molybdenum deposit belt and their implication to genetic mechanism and type

    Institute of Scientific and Technical Information of China (English)

    陈衍景; 李超; 张静; 李震; 王海华

    2000-01-01

    A great deal of Mesozoic hypobatholithic granites and hypabyssal porphyries develop in the Qinling Mountains. The former has long been regarded as transformation type (or S-type), and the latter associated with Mo-mineralization regarded as syntexis type (or l-type) granitoids. Statistics show that Sr, andδ18O of hypabyssal porphyries respectively range from 0.705 to 0.714, and from 7.2‰ to 12.1‰, agreeing with those of hypobatholithes (Sr1=0.705-0.710, δ18O = 6.1‰-10.4‰), which indicates that they share similar material sources and petrogenic mechanism. Based on analysis of lithological, mineralogical and geochemical characteristics of these granitoids and on study of their petrogenic tectonic background and regional geophysical data, we argue that both the shallow-seated porphyries and deep-seated batholithes were the products of Mesozoic collision between South China and North China paleocontinents. Subsequently, all these granti-toids should be attributed to collision type.

  7. In situ Sr/Sr investigation of igneous apatites and carbonates using laser-ablation MC-ICP-MS

    DEFF Research Database (Denmark)

    Bizzarro, Martin; Simonetti, A.; Stevenson, R.K.;

    2003-01-01

    In situ Sr isotopic compositions of coexisting apatite and carbonate for carbonatites from the Sarfartoq alkaline complex, Greenland, have been determined by laser-ablation multicollector inductively coupled plasma mass spectrometry. This study is the first to examine the extent of Sr isotopic...... (regional) scale open-system processes, possibly involving mixing of carbonatitic melts derived from distinct mantle sources or from a common isotopically heterogeneous mantle. Copyright © 2003 Elsevier Science Ltd....

  8. Experiences with the determination of Sr-89 and Sr-90 using fast methods; Erfahrungen bei der Bestimmung von {sup 89}Sr und {sup 90}Sr mittels Schnellmethoden

    Energy Technology Data Exchange (ETDEWEB)

    Kowalik, C.; Fueger, J. [Thueringer Landesanstalt fuer Umwelt und Geologie, Jena (Germany). Landesmessstelle fuer Umweltradioaktivaet

    2014-01-20

    Quick methods of the measurement of {sup 89}Sr and {sup 90}Sr have a great importance in the supervision of the environmental radioactivity. It is necessary to receive in short time dependable analytical data to be able to carry out suitable assessments or to give recommendations. The aim of the investigations was to be guaranteed the demands for these methods (test preparation, measurement and evaluation). The use of the solid phase extraction by means of commercial Sr Resin trademark columns (4.4' (5')-Di-tert-butylcyclohexanol-18-kronen-6-aether) (Triskem) to the radiochemical separation of the Sr isotopes was suitable. The measurements occurred to the FHT 770 T12 - Multi Low Level Alpha/Beta Sample Counter (Thermo Scientific). The results contain the summary activities of all available Sr isotopes, as for example {sup 89}Sr and {sup 90}Sr. The calculations of the single activities occur about the mathematical algorithm of the linear development on the basis of the works of G. Kanisch. The first results show, this method is suitable for the analysis of {sup 89}Sr and {sup 90}Sr and is used therefore in future in Thuringia.

  9. Geochronological synthesis of Bahia state and the crustal evolution, based in evolution diagram of Sr and initial rate of Sr87/Sr86

    International Nuclear Information System (INIS)

    The crustal evolution of the ancient terrains of the State of Bahia, Brazil, is attempted with the aid of Sr isotopic results as natural tracers. Some Nd and Pb isotopic data are also available, and support the main conclusions based on Sr evolution diagrams. The analysis of the Sr evolution diagrams shows that the Archean Terrains are mainly formed by accretion from mantle-derived material, but crustal reworking is indicated by the high initial 87Sr/86Sr value of the Jequie Complex. The Transamazonian mobile belt include both types of materials, but the 87Sr/86Sr value, generally lower than those of the Jequie Complex, markes improbable a direct derivation. During Middle and Late Proterozoic, the continental crust was already well consolidated, and reworking of crustal material predominated within the Espinhaco and Brasiliano folded systems

  10. C, O, Sr and Nd isotope systematics of carbonates of Papaghni sub-basin, Andhra Pradesh, India: Implications for genesis of carbonate-hosted stratiform uranium mineralisation and geodynamic evolution of the Cuddapah basin

    Science.gov (United States)

    Absar, Nurul; Nizamudheen, B. M.; Augustine, Sminto; Managave, Shreyas; Balakrishnan, S.

    2016-10-01

    The Cuddapah basin (CB) is one of a series of Proterozoic basins that overlie the Archaean cratons of India, and contains a unique stratiform carbonate-hosted uranium mineralisation. In the present work, we discuss stable (C, O) and radiogenic (Nd, Sr) isotope systematics of carbonates of the Papaghni sub-basin in order to understand uranium ore forming processes and geodynamic evolution of the CB. Uranium mineralised dolomites (UMDs) of the basal Vempalle Formation show a significantly lighter (~ 1.5‰) C-isotope signature compared to that of open-marine stromatolitic sub-tidal facies, suggesting input of isotopically lighter carbon through in situ remineralisation of organic matter (OM). This implies deposition in a hydrologically-restricted, redox-stratified lagoonal basin wherein exchange with open oceanic dissolved inorganic carbon (DIC) was limited. Persistent bottom water anoxia was created and maintained through consumption of dissolved oxygen (DO) by decaying OM produced in oxidised surface water zone. Significantly more radiogenic εNd(t) of UMD (- 6.31 ± 0.54) compared to that of Dharwar upper crust (- 8.64 ± 3.11) indicates that dissolved constituents did not originate from the Dharwar craton, rather were derived from more juvenile exotic sources - possibly from a continental arc. Dissolved uranyl ions (U+ 6) were introduced to the basin through fluvial run-off and were reduced to immobile uranous ions (U+ 4) at the redox interface resulting in precipitation of pitchblende and coffinite. Carbonate horizons of upper Vempalle Formation and Tadpatri Formation show progressively more radiogenic Nd isotope compositions signifying increased juvenile arc contribution to the Papaghni sub-basin through time, which is also corroborated by the presence of younger zircons (1923 ± 22 Ma) in Pulivendla quartzites. We propose that the Papaghni sub-basin opened as a back-arc extensional basin at ~ 2 Ga as a result of westerly-directed subduction of oceanic crust

  11. Penning-trap mass spectrometry of highly charged, neutron-rich Rb and Sr isotopes in the vicinity of $A\\approx100$

    CERN Document Server

    Simon, V V; Chowdhury, U; Eberhardt, B; Ettenauer, S; Gallant, A T; Mané, E; Simon, M C; Delheij, P; Pearson, M R; Audi, G; Gwinner, G; Lunney, D; Schatz, H; Dilling, J

    2012-01-01

    The neutron-rich mass region around $A\\approx100$ presents challenges for modeling the astrophysical $r$-process because of rapid shape transitions. We report on mass measurements using the TITAN Penning trap at TRIUMF-ISAC to attain more reliable theoretical predictions of $r$-process nucleosynthesis paths in this region. A new approach using highly charged ($q=15+$) ions has been applied which considerably saves measurement time and preserves accuracy. New mass measurements of neutron-rich $^{94,97,98}$Rb and $^{94,97-99}$Sr have uncertainties of less than 4 keV and show deviations of up to 11$\\sigma$ to previous measurements. An analysis using a parameterized $r$-process model is performed and shows that mass uncertainties for the A=90 abundance region are eliminated.

  12. Sr/Ca and stable isotopes in a coral from the Venezuelan coast: A record of 20th-century changes in SST, SSS and cloud cover?

    Science.gov (United States)

    Hetzinger, S.; Pfeiffer, M.; Dullo, W.; Zinke, J.; Garbe-Schoenberg, C.

    2011-12-01

    We present a record of monthly δ18O and Sr/Ca variations in coral aragonite from a massive Diploria strigosa colony retrieved from a coastal NW-Venezuelan reef site (10.55°N, 67.24°W; 1940-2004). Linear regression of coral proxies to high resolution satellite sea surface temperature (SST) data (NASA OBPG MODIS-Aqua, 9-km resolution) demonstrates that both geochemical proxies record seasonal temperature variability in ambient seawater (Sr/Ca: r=-0.68 monthly, r=-0.60 annual; δ18O: r=-0.57 monthly, r=-0.46 annual; 1985-2004). On longer time scales both proxies record local as well as regional SST dynamics in the southeastern Caribbean and northern North Tropical Atlantic. A statistically significant relationship is observed between coral δ18O and local air temperature (r=-0.56; 1951-2002), while correspondence of δ18O to SST products (e.g. ERSST, SODA reanalysis) is lower than for Sr/Ca ratios. However, coral δ18O is a function of both temperature and δ18Oseawater and δ18Oseawater in turn is dependent on salinity. A comparison of δ18O to sea surface salinity (SSS) data confirms the existence of a strong salinity component in coral δ18O on annual and longer time scales (SODA reanalysis, r=0.65 for annual means, r=0.84 for 3-year average; 1958-2001). A decreasing trend from the mid-1980s onwards is evident in both SSS and coral δ18O, corresponding to trends seen in other Caribbean studies. Further, both geochemical proxies show a significant negative correlation to cloud cover averaged over a regional box (r=-0.66 for Sr/Ca; r=-0.48 for δ18O; 1941-2003). A significant drop in cloud cover is seen around the year 1947, which is displayed in both proxies as a distinct positive peak and coincides with a drop in instrumental SST. Interestingly, a marked decrease in annual coral growth rate is observed in the uppermost years of the core (1999 to 2004), as well as a reduced seasonal amplitude in δ18O variability and a trend to more negative δ18O-values at the

  13. Integrating isotopic fingerprinting with petrology: how do igneous rocks evolve?

    Science.gov (United States)

    Davidson, J. P.

    2002-12-01

    In the title of his seminal work, N.L. Bowen recognized the fundamental importance of magmatic evolution in producing the spectrum of igneous rocks. Indeed it is difficult to imagine a hot highly reactive fluid passing through c. 100 km of a chemically distinct medium (lithosphere) without evolving through cooling, crystallization and interaction with the wall rocks. The fact that magmas evolve - almost invariably through open system processes - has been largely marginalized in the past 30 years by the desire to use them as probes of mantle source regions. This perspective has been driven principally by advances offered by isotope geochemistry, through which components and sources can be effectively fingerprinted. Two fundamental observations urge caution in ignoring differentiation effects; 1) the scarcity of truly primary magmas according to geochemical criteria (recognized long ago by petrologists), and 2) the common occurrence of petrographic criteria attesting to open system evolution. Recent advances in multicollector mass spectrometry permit integration of the powerful diagnostic tools of isotope geochemistry with petrographic observations through accurate and precise analysis of small samples. Laser ablation and microdrilling enable sampling within and between mineral phases. The results of our microsampling investigations give widespread support for open system evolution of magmas, and provide insights into the mechanisms and timescales over which this occurs. For example; 1) core-rim decreases in 87Sr/86Sr in zoned plagioclase crystals from 1982 lavas of El Chichon volcano, Mexico, argue that the zoning and isotopic changes are in response to magma recharge mixing with an originally contaminated resident magma; 2) Single grain and intra-grain isotopic analyses of mineral phases from Ngauruhoe andesites (New Zealand) are highly variable, arguing that bulk rock data reflect mechanical aggregations of components which have evolved in discrete domains of the

  14. Chronology, geochemistry and Sr-Nd isotope studies of Jurassic intrusions in the Diyanqinamu porphyry Mo mine, central Inner Mongolia, China

    Science.gov (United States)

    Sun, Hairui; Huang, Zhilong; Li, Wenbo; Leng, Chengbiao; Ma, Deyun; Zhang, Xingchun

    2014-07-01

    Available cores of porphyritic granite and aplitic granite from the Diyanqinamu porphyry Mo deposit in the north central Great Xing’an Range presented an opportunity to examine and analyze Mesozoic igneous rocks far from the Paleo-Pacific subduction zone. The Diyanqinamu granites are highly fractionated I-type, distinguished from the M-, A- or S-type granite by: high SiO2, and Rb; low Zr, Nb, Y, and Ce; low Fe2O3total/MgO and (K2O + Na2O)/CaO ratios; low alumina saturation index (Haker diagrams; low Ba, Sr, Nb, P, Ti, Eu; linear relationship in both (La/Yb)N vs. La and Sr vs. Ba diagrams; and, decreasing LREE and ∑REE with increasing SiO2. The Diyanqinamu granites have young depleted-mantle two-stage model ages (avg. TDM2 = 660 Ma) similar to those of most Mesozoic voluminous felsic magmas in northeastern China, and were likely sourced from pre-existent crustal components both “old” and juvenile that had been juxtaposed during the tectonic evolution of the Paleo-Asian Ocean. These granites project in the transitional field from syn-collision to post-collision tectonic settings on tectonic discrimination diagrams, implying emplacement in an extensional environment. Extensional volcanism and basin formation in the Great Xing’an Range region in Late Jurassic is coeval with the Diyanqinamu granites, demonstrating that post-orogenic lithospheric extension related to the closure of the Mongol-Okhotsk Ocean was the main driving force for Late Jurassic magmatism in this region.

  15. Petrogenesis of subvolcanic rocks from the Khunik prospecting area, south of Birjand, Iran: Geochemical, Sr-Nd isotopic and U-Pb zircon constraints

    Science.gov (United States)

    Samiee, Somayeh; Karimpour, Mohammad Hassan; Ghaderi, Majid; Haidarian Shahri, Mohammad Reza; Klöetzli, Urs; Santos, José Francisco

    2016-01-01

    The Khunik prospecting area is located 106 km south of Birjand in eastern Iran, and is considered as an epithermal gold prospecting area. The mineralization is related to subvolcanic rocks. There are several outcrops of subvolcanic intrusions in the area which intruded into Paleocene-Eocene volcanic rocks (andesite, trachy-andesite and pyroclastic rocks). Petrographic studies indicate that subvolcanic rocks consist mainly of diorite, monzonite, quartz-monzonite, monzodiorite and quartz-monzodiorite. Mineralogically, these rocks contain plagioclase, K-feldspar, amphibole, pyroxene, biotite and quartz. Geochemically, they have features typical of high-K calk-alkaline to shoshonitic and are metaluminous, and also belong to magnetite granitoid series (I-type). Primitive mantle normalized trace element spider diagrams display enrichment in LILE, such as Rb, Ba, and Cs, compared to HFSE. Chondrite-normalized REE plots show moderately LREE enriched patterns (7.45 diagrams also show affinities with modern convergent margin magmas, suggesting that magmas of Khunik area formed in volcanic arc setting related to subduction of the oceanic crust under the Lut Block plate. The initial 87Sr/86Sr ratios (0.704196-0.704772) and εNdi values (+1.3 to +3.3) are compatible with an origin of the parental melts in a supra-subduction mantle wedge. Zircon U-Pb dating by LA-ICP-MS indicates the age of 38 ± 1 Ma (late Eocene) for subvolcanic units that are related to mineralization. A biotite granodiorite porphyry is the testimony of the youngest magmatic activity in the area, with an age of 31 ± 1 Ma (early Oligocene). The represented dates are interpreted as magmatic crystallization ages of subvolcanic intrusions.

  16. Mantle-like Sr-Nd isotope composition of Fe-K subalkaline granites : the Peneda-Gerês Variscan massif (NW Iberian Peninsula)

    OpenAIRE

    Mendes, Anabela Carreira; Dias, G.

    2004-01-01

    The Peneda-Gerês massif is one of the most representative NW Iberian late- to post-orogenic Variscan granitic plutons. It resulted essentially from the subsynchronous emplacement, at 290-296 Ma, of two granitic magmas of Fe-K subalkaline affinity, with primitive isotopic composition: Sri = 0.703-0.707 and eNdi = -1.5 to -2.4. An origin by mantle input followed by mantle-crust interactions is proposed, implying the contribution of a less enriched mantle component than that involved in the gene...

  17. 40Ar/39Ar Geochronology, Isotope Geochemistry (Sr, Nd, Pb), and petrology of alkaline lavas near Yampa, Colorado: migration of alkaline volcanism and evolution of the northern Rio Grande rift

    Science.gov (United States)

    Cosca, Michael A.; Thompson, Ren A.; Lee, John P.; Turner, Kenzie J.; Neymark, Leonid A.; Premo, Wayne R.

    2014-01-01

    Volcanic rocks near Yampa, Colorado (USA), represent one of several small late Miocene to Quaternary alkaline volcanic fields along the northeast margin of the Colorado Plateau. Basanite, trachybasalt, and basalt collected from six sites within the Yampa volcanic field were investigated to assess correlations with late Cenozoic extension and Rio Grande rifting. In this paper we report major and trace element rock and mineral compositions and Ar, Sr, Nd, and Pb isotope data for these volcanic rocks. High-precision 40Ar/39Ar geochronology indicates westward migration of volcanism within the Yampa volcanic field between 6 and 4.5 Ma, and the Sr, Nd, and Pb isotope values are consistent with a primary source in the Proterozoic subcontinental lithospheric mantle. Relict olivine phenocrysts have Mg- and Ni-rich cores, whereas unmelted clinopyroxene cores are Na and Si enriched with finely banded Ca-, Mg-, Al-, and Ti-enriched rims, thus tracing their crystallization history from a lithospheric mantle source region to one in contact with melt prior to eruption. A regional synthesis of Neogene and younger volcanism within the Rio Grande rift corridor, from northern New Mexico to southern Wyoming, supports a systematic overall southwest migration of alkaline volcanism. We interpret this Neogene to Quaternary migration of volcanism toward the northeast margin of the Colorado Plateau to record passage of melt through subvertical zones within the lithosphere weakened by late Cenozoic extension. If the locus of Quaternary alkaline magmatism defines the current location of the Rio Grande rift, it includes the Leucite Hills, Wyoming. We suggest that alkaline volcanism in the incipient northern Rio Grande rift, north of Leadville, Colorado, represents melting of the subcontinental lithospheric mantle in response to transient infiltration of asthenospheric mantle into deep, subvertical zones of dilational crustal weakness developed during late Cenozoic extension that have been

  18. Petrogenesis of the Yaochong granite and Mo deposit, Western Dabie orogen, eastern-central China: Constraints from zircon U-Pb and molybdenite Re-Os ages, whole-rock geochemistry and Sr-Nd-Pb-Hf isotopes

    Science.gov (United States)

    Chen, Wei; Xu, Zhaowen; Qiu, Wenhong; Li, Chao; Yu, Yang; Wang, Hao; Su, Yang

    2015-05-01

    The Dabie orogen is among the most famous continent-continent collisional orogenic belts in the world, and is characterized by intensive post-collisional extension, magmatism and Mo mineralization. However, the genetic links between the mineralization and the geodynamic evolution of the orogen remain unresolved. In this paper, the Yaochong Mo deposit and its associated granitic stocks were investigated to elucidate this issue. Our new zircon U-Pb ages yielded an Early Cretaceous age (133.3 ± 1.3 Ma) for the Yaochong granite, and our molybdenite Re-Os dating gave a similar age (135 ± 1 Ma) for the Mo deposit. The Yaochong stock is characterized by high silica and alkali but low Mg, Fe and Ca. It is enriched in light rare earth elements (LREEs) and large ion lithophile elements (LILEs: Rb, K, Th and U), but strongly depleted in heavy REEs, and high field strength elements (HFSEs: Nb, Ta, Ti and Y). The Yaochong granite has initial 87Sr/86Sr ratios of 0.7087-0.7096, and Pb isotopic ratios of (206Pb/204Pb)i = 16.599-16.704, (207Pb/204Pb)i = 15.170-15.618 and (208Pb/204Pb)i = 36.376-38.248. The granite has εNd(t) of -18.0 to -16.3 and εHf(t) values of -26.5 to -20.0. All these data indicate that the Yaochong granite is a high-K calc-alkaline fractionated I-type granite, and may have originated from partial melting of the thickened Yangtze continental crust. The Mo ores also show low radiogenic Pb isotopes similar to the Yaochong stock. Medium Re content in molybdenite (21.8-74.8 ppm) also suggests that the ore-forming materials were derived from the thickened lower crust with possibly minor mixing with the mantle. Similar to the Eastern Dabie orogen, the thickened crust beneath the Western Dabie orogen may also have experienced tectonic collapse, which may have exerted fundamental geodynamic controls on the two-stage Mo mineralization in the region.

  19. Determination of the geographic origin of rice by chemometrics with strontium and lead isotope ratios and multielement concentrations.

    Science.gov (United States)

    Ariyama, Kaoru; Shinozaki, Miyuki; Kawasaki, Akira

    2012-02-22

    The objective of this study was to develop a technique for determining the country of origin of rice in the Japanese market. The rice samples included a total of 350 products grown in Japan (n = 200), the United States (n = 50), China (n = 50), and Thailand (n = 50). In this study, (87)Sr/(86)Sr and Pb isotope ((204)Pb, (206)Pb, (207)Pb, and (208)Pb) ratios and multielement concentrations (Al, Fe, Co, Ni, Cu, Rb, Sr, and Ba) were determined by high-resolution inductively coupled plasma mass spectrometry. By combining three chemometric techniques based on different principles and determination criteria, the countries of origin of rice were determined. The predictions made by 10-fold cross-validation were around 97% accurate. The presented method demonstrated the effectiveness of determining the geographic origin of an agricultural product by combining several chemometric techniques using heavy element isotope ratios and multielement concentrations.

  20. Late Cenozoic volcanism in the western Woodlark Basin area, SW Pacific: the sources of marine volcanic ash layers based on their elemental and Sr-Nd isotope compositions

    Science.gov (United States)

    Lackschewitz, K. S.; Mertz, D. F.; Devey, C. W.; Garbe-Schönberg, C.-D.

    2002-12-01

    Tephra fallout layers and volcaniclastic deposits, derived from volcanic sources around and on the Papuan Peninsula, form a substantial part of the Woodlark Basin marine sedimentary succession. Sampling by the Ocean Drilling Program Leg 180 in the western Woodlark Basin provides the opportunity to document the distribution of the volcanically-derived components as well as to evaluate their chronology, chemistry, and isotope compositions in order to gain information on the volcanic sources and original magmatic systems. Glass shards selected from 57 volcanogenic layers within the sampled Pliocene-Pleistocene sedimentary sequence show predominantly rhyolitic compositions, with subordinate basaltic andesites, basaltic trachy-andesites, andesites, trachy-andesites, dacites, and phonolites. It was possible to correlate only a few of the volcanogenic layers between sites using geochemical and age information apparently because of the formation of strongly compartmentalised sedimentary realms on this actively rifting margin. In many cases it was possible to correlate Leg 180 volcanic components with their eruption source areas based on chemical and isotope compositions. Likely sources for a considerable number of the volcanogenic deposits are Moresby and Dawson Strait volcanoes (D'Entrecasteaux Islands region) for high-K calc-alkaline glasses. The Dawson Strait volcanoes appear to represent the source for five peralkaline tephra layers. One basaltic andesitic volcaniclastic layer shows affinities to basaltic andesites from the Woodlark spreading tip and Cheshire Seamount. For other layers, a clear identification of the sources proved impossible, although their isotope and chemical signatures suggest similarities to south-west Pacific subduction volcanism, e.g. New Britain and Tonga-Kermadec island arcs. Volcanic islands in the Trobriand Arc (for example, Woodlark Island Amphlett Islands and/or Egum Atoll) are probable sources for several volcaniclastic layers with ages

  1. Major and trace element and Sr and Nd isotopic results from mantle diapirs in the Oman ophiolite: Implications for off-axis magmatic processes

    Science.gov (United States)

    Nicolle, Marie; Jousselin, David; Reisberg, Laurie; Bosch, Delphine; Stephant, Aurore

    2016-03-01

    The Oman ophiolite includes both a fossil fast spreading axis, defined by five mantle diapirs, and an off-axis mantle diapir emplaced 30 km from the axis, providing a natural laboratory for the study of off-axis magmatic processes. We compare field and petrological observations coupled with geochemical and isotopic analyses of samples from the off-axis diapir with those of the nearest on-axis diapir, with a particular focus on the Moho Transition Zone (MTZ). Both diapirs are defined by the presence of steeply plunging lineations, but in the on-axis case, these lineations rotate gradually into parallelism with the horizontal magmatic lineations of the overlying crust, while in the off-axis case, a shear zone separates the steeply plunging lineations from the horizontal lineations of the surrounding mantle. In the on-axis diapir, the MTZ is 50 to 500 m thick and composed of dunite with layered gabbro lenses whereas in the off-axis diapir, the MTZ is thicker and composed of dunite with massive (∼20% of MTZ) clinopyroxenite lenses and a notable absence of plagioclase. Moreover, the off-axis diapir is associated with amphibole-bearing intrusions, consisting of Mg-rich gabbroic sills in the mantle peripheral to the diapir, and microgabbroic lenses of broadly basaltic composition in the overlying crust. The εNd values of the pyroxenites in the MTZ of the off-axis diapir fully overlap with those of the intrusions in the surrounding mantle and crust, suggesting that they are genetically related. Calculated rare earth element (REE) abundances of liquids in equilibrium with clinopyroxene imply that the magmas that traversed the MTZ of the off-axis diapir were more depleted in highly incompatible elements than their counterparts in the MTZ of the on-axis diapir. On the other hand, Nd isotopic compositions of the off-axis samples (ε Nd = 6.2- 7.9 in 18 of 19 samples) indicate derivation of their parental magmas from a less depleted source than that which produced the magma

  2. Zircon U-Pb geochronology and Sr-Nd isotopes of volcanic rocks from the Dahalajunshan Formation: implications for Late Devonian-Middle Carboniferous tectonic evolution of the Chinese Western Tianshan

    Science.gov (United States)

    Yu, Xinqi; Wang, Zongxiu; Zhou, Xiang; Xiao, Weifeng; Yang, Xinpeng

    2016-07-01

    The widespread Late Devonian-Middle Carboniferous volcanic rocks in the Chinese Western Tianshan provide important constraints on the subduction history of the South Tianshan oceanic lithosphere. Here, we investigate the basalt, basaltic andesite, andesite, trachyandesite, and rhyolite from the Dahalajunshan Formation from Western Tianshan. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) U-Pb zircon geochronology constrains their age of formation to between 376 and 333 Ma (i.e., Late Devonian-Middle Carboniferous) with distinct variation in space (from west to east) and time (from early to late). Based on geochemical, zircon geochronological, and Sr-Nd isotopic data, we demonstrate that the Dahalajunshan volcanic was generated in a continental arc setting associated with the subduction of the south Tianshan Ocean during Late Devonian to Middle Carboniferous. The volcanic rocks belonging to Dahalajunshan Formation in the northwestern part of the Yili Block suggest that the northward subduction of the south Tianshan Ocean was initiated in the Early Devonian; those in the southern and eastern part of the Yili Block were probably produced by a northward subduction of South Tianshan Ocean during Late Devonian to Middle Carboniferous.

  3. 东准噶尔晚古生代次火山侵入岩锆石SHRIMP U-Pb年龄及Sr-Nd同位素地球化学%Zircon SHRIMP U-Pb Dating and Sr-Nd Isotopic Geochemistry of Late Paleozoic Subvolcanic-Intrusive Rocks in Eastern Junggar

    Institute of Scientific and Technical Information of China (English)

    张峰; 徐涛; 郭晓东; 范俊杰; 张栋; 潘爱军; 朝银银

    2014-01-01

    Late Paleozoicvolcanic-subvolcanic-intrusive rocks in Eastern Junggar are developed.Songkaersu granodiorite porphyry,as a part of them,formed in the southeast Kalamali tectonic belt.Petrography,SHRIMP zircon U-Pb and Sr-Nd isotope indicate that all zircons selected are magmatic, and the zircons U-Pb concordant ages of two samples may be sub-divided into many groups,of which the youngest concordant age is 305.5~316.3Ma which can be interpreted as the for-mation age of Songkaersu granodiorite porphyry.On the other hand,others ages such as early Cambrian to early Carbonif-erou are consistent with the ages of oceanic-crust and island-arc magmatic rocks around the Junggar Basin.Moreover,the positiveεNd(t)(3.0 to 15.1), medium 87Sr/86Sr initial ratios (0.703 861 to 0.713 151), and smaller T2DM (412 to 839) may imply that the eastern basement of the Junggar Basin was tectonically amalgamated by underplating of mantle-derived substances and different Paleozoic remnant oceanic crust and arc complexes upon the minor Precambrian continental crust . Songkaersu granodiorite porphyry may result from the interaction of a amount of new-born lower crust and minor asthenospheric mantle or depleted lithospheric mantle,and the formation mechanism of them perhaps might be related to the subduction of the Paleo-Asian oceanic plate under the Kazakhstan-Junggar plate and result in back-arc spreading.%东准噶尔地区石炭纪巴塔玛依内山组火山岩-次火山侵入岩发育。本文以卡拉麦里构造带东南部松喀尔苏地区次火山侵入岩--花岗闪长斑岩为研究对象,通过岩石学、SHRIMP锆石U-Pb和Sr-Nd同位素方面的研究发现,所有锆石都具岩浆成因,锆石U-Pb年龄可分为多组,其中最小的一组年龄为305.5~316.3 Ma,代表岩体的形成时间,其他年龄多与准噶尔地区产出的具洋壳和岛弧性质的岩浆岩时代一致。岩石具正的εNd(t)(3.0~15.1),中等的87Sr/86Sr初始值(0

  4. Paleoenvironments in Meso-Neoproterozoic carbonates of the Mbuji-Mayi Supergroup (Democratic Republic of Congo) - Microfacies analysis combined with C-O-Sr isotopes, major-trace elements and REE + Y distributions

    Science.gov (United States)

    Delpomdor, F.; Blanpied, C.; Virgone, A.; Préat, A.

    2013-12-01

    The Meso- and Neoproterozoic Mbuji-Mayi Supergroup (1155 Ma to ca. 800 Ma) was deposited in the SE-NW trending siliciclastic-carbonate failed-rift in the Sankuru-Mbuji-Mayi-Lomami-Lovoy Basin. Drillcore- and outcrop-derived microfacies, isotope (C, O and Sr) compositions of carbonates and REE + Y distributions are integrated to unravel the paleoenvironmental and chemical conditions prevailing during deposition and alteration (or contamination) of the Mbuji-Mayi carbonates. The carbonate succession (BIe subgroup and BIIa to BIIe subgroups), composed of 11 microfacies (MF), records the evolution of a marine ramp submitted to evaporation, with basinal and low-energy outer-ramp environments (MF1-MF5), biohermal mid-ramp (MF6) and restricted tide-dominated lagoon inner-ramp (MF7-MF9) settings, overlain by lacustrine (MF10) and sabkha (MF11) environments. The ramp margin is characterized by thick stacks of stromatolitic bioherms. δ13C and δ18O relationships in the Mbuji-Mayi carbonates allow discrimination between meteoric (δ13C: -7.5‰ to +0.0‰, δ18O: -7.0‰ to -1.0‰) and burial lithifications (δ13C: -1.5‰ to +0.0‰, δ18O: -15.1‰ to -7.0‰), that overprinted a primary marine signal (δ13C: -1.5‰ to +2.0‰, δ18O: -3.0‰ to +0.5‰) partially preserved in the subgroups. Unaltered pristine signals are found in the Mbuji-Mayi carbonates with 87Sr/86Sr ratios (0.7065-0.7082) similar to those of the marine-preserved strontium signatures of the early Neoproterozoic oceans. The PAAS-normalized REE + Y distributions indicate that the BIe carbonates were altered by Fe-oxide-rich hydrothermal fluids. BIIb and BIIe carbonates exhibit uniform light REE depleted patterns suggesting inputs of detrital river material whereas a marine seawater, highlighted by the REE + Y distributions is preserved in BIIc and BIId carbonates. The pattern of carbon, oxygen and strontium isotopic variations in the Mbuji-Mayi carbonates reflects deposition and early diagenesis in

  5. Geochemical, zircon U-Pb dating and Sr-Nd-Hf isotopic constraints on the age and petrogenesis of an Early Cretaceous volcanic-intrusive complex at Xiangshan, Southeast China

    Science.gov (United States)

    Yang, Shui-Yuan; Jiang, Shao-Yong; Jiang, Yao-Hui; Zhao, Kui-Dong; Fan, Hong-Hai

    2011-01-01

    The Late Mesozoic geology of Southeast China is characterized by extensive Jurassic to Cretaceous magmatism consisting predominantly of granites and rhyolites and subordinate mafic rocks, forming a belt of volcanic-intrusive complexes. The Xiangshan volcanic-intrusive complex is located in the NW region of the belt and mainly contains the following lithologies: rhyodacite and rhyodacitic porphyry, porphyritic lava, granite porphyry with mafic microgranular enclaves, quartz monzonitic porphyry, and lamprophyre dyke. Major and trace-element compositions, zircon U-Pb dating, and Sr-Nd-Hf isotopic compositions have been investigated for these rocks. The precise SHRIMP and LA-ICP-MS zircon U-Pb dating shows that the emplacement of various magmatic units at Xiangshan took place within a short time period of less than 2 Myrs. The stratigraphically oldest rhyodacite yielded a zircon U-Pb age of 135 ± 1 Ma and the overlying rhyodacitic porphyry has an age of 135 ± 1 Ma. Three porphyritic lava samples yielded zircon U-Pb ages of 136 ± 1 Ma, 132 ± 1 Ma, and 135 ± 1 Ma, respectively. Two subvolcanic rocks (granite porphyry) yielded zircon U-Pb ages of 137 ± 1 Ma and 137 ± 1 Ma. A quartz monzonitic porphyry dyke, which represented the final stage of magmatism at Xiangshan, also yielded a zircon U-Pb age of 136 ± 1 Ma. All these newly obtained precise U-Pb ages demonstrate that the entire magmatic activity at Xiangshan was rapid and possibly took place at the peak of extensional tectonics in SE China. The geochemical data indicate that all these samples from the volcanic-intrusive complex have an A-type affinity. Sr-Nd-Hf isotopic data suggest that the Xiangshan volcanic-intrusive complex derived mainly from remelting of Paleo-Mesoproterozoic crust without significant additions of mantle-derived magma. However, the quartz monzonitic porphyry, which has zircon Hf model ages older than the whole-rock Nd model ages, and which has ɛNd(T) value higher than the other rocks

  6. Sr-Nd-Hf isotopes of the intrusive rocks in the Cretaceous Xigaze ophiolite, southern Tibet: Constraints on its formation setting

    Science.gov (United States)

    Zhang, Liang-Liang; Liu, Chuan-Zhou; Wu, Fu-Yuan; Zhang, Chang; Ji, Wei-Qiang; Wang, Jian-Gang

    2016-08-01

    The Cretaceous Xigaze ophiolite is best exposed at the central part of the Yarlung-Zangbo Suture Zone, Tibet Plateau. It consists of a thick section of mantle peridotites, but a relatively thin mafic sequence. This study presents geochronological and geochemical data for intrusive dykes (both mafic and felsic) and basalts to revisit the formation setting of the Xigaze ophiolite. The rodingites are characterized by high CaO and low Na2O contents relative to mafic dykes and show big variations in trace element compositions. Both gabbros and diabases have similar geochemical compositions, with MgO contents of 6.42-11.48 wt% and Mg# of 0.56-0.71. They display REE patterns similar to N-MORB and are variably enriched in large ion lithophile elements. Basalts have fractionated compositions and display LREE-depleted patterns very similar to N-MORB. They do not show obvious enrichment in LILE and depletion in high-field-strength elements, but a negative Nb anomaly is present. The studied plagiogranites have compositions of trondhjemite to tonalite, with high Na2O and low K2O contents. They have low TiO2 contents less than 1 wt%, consistent with melts formed by anatexis of gabbros rather than by differentiation of basalts. Zircons from seven samples, including three rodingites, three plagiogranites, and one gabbro, have been dated and yielded U-Pb ages of 124.6 ~ 130.5 Ma, indicating the Xigaze ophiolite was formed during the Early Cretaceous. They have mantle-like δ18O values of + 4.92 ~ + 5.26‰ and very positive εHf(t) values of + 16 ~ + 13.3. Ages of the rodingites and less altered gabbros indicate that serpentinization was occurred at ~ 125 Ma. Occurrence of both gabbroic and diabase dykes within the serpentinites suggests that the mantle lithosphere of the Xigaze ophiolite was rapidly exhumed. Both mafic and felsic dykes have slightly more radiogenic 87Sr/86Sr ratios relative to MORB, but depleted Hf-Nd isotpe compositions. They have a limited range of ε

  7. Zircon U-Pb and molybdenite Re-Os geochronology and Sr-Nd-Pb-Hf isotopic constraints on the genesis of the Xuejiping porphyry copper deposit in Zhongdian, Northwest Yunnan, China

    Science.gov (United States)

    Leng, Cheng-Biao; Zhang, Xing-Chun; Hu, Rui-Zhong; Wang, Shou-Xu; Zhong, Hong; Wang, Wai-Quan; Bi, Xian-Wu

    2012-10-01

    The Xuejiping porphyry copper deposit is located in northwestern Yunnan Province, China. Tectonically, it lies in the southern part of the Triassic Yidun island arc. The copper mineralization is mainly hosted in quartz-dioritic and quartz-monzonitic porphyries which intruded into clastic-volcanic rocks of the Late Triassic Tumugou Formation. There are several alteration zones including potassic, strong silicific and phyllic, argillic, and propylitic alteration zones from inner to outer of the mineralized porphyry bodies. The ages of ore-bearing quartz-monzonitic porphyry and its host andesite are obtained by using the zircon SIMS U-Pb dating method, with results of 218.3 ± 1.6 Ma (MSWD = 0.31, N = 15) and 218.5 ± 1.6 Ma (MSWD = 0.91, N = 16), respectively. Meanwhile, the molybdenite Re-Os dating yields a Re-Os isochronal age of 221.4 ± 2.3 Ma (MSWD = 0.54, N = 5) and a weighted mean age of 219.9 ± 0.7 Ma (MSWD = 0.88). They are quite in accordance with the zircon U-Pb ages within errors. Furthermore, all of them are contemporary with the timing of the Garzê-Litang oceanic crust subduction in the Yidun arc. Therefore, the Xuejiping deposit could be formed in a continental margin setting. There are negative ɛNd(t) values ranging from -3.8 to -2.1 and relatively high initial 87Sr/86Sr ratios from 0.7051 to 0.7059 for the Xuejiping porphyries and host andesites. The (206Pb/204Pb)t, (207Pb/204Pb)t and (208Pb/204Pb)t values of the Xuejiping porphyries and host andesites vary from 17.899 to 18.654, from 15.529 to 15.626, and from 37.864 to 38.52, respectively, indicative of high radiogenic Pb isotopic features. In situ Hf isotopic analyses on zircons by using LA-MC-ICP-MS exhibit that there are quite uniform and slightly positive ɛHf(t) values ranging from -0.2 to +3.2 (mostly between 0 and +2), corresponding to relatively young single-stage Hf model ages from 735 Ma to 871 Ma. These isotopic features suggest that the primary magmas of the Xuejiping porphyries and

  8. Strontium isotope characterization of wines from Quebec, Canada.

    Science.gov (United States)

    Vinciguerra, Victor; Stevenson, Ross; Pedneault, Karine; Poirier, André; Hélie, Jean-François; Widory, David

    2016-11-01

    The (87)Sr/(86)Sr isotope ratios were measured on grape, wine and soil samples collected in 13 commercial vineyards located in three major wine producing areas of Quebec (Canada). The soils yield Sr isotope ratios that are intimately related to the local geology and unambiguously discriminate the different producing areas. A strong relationship exists between the (87)Sr/(86)Sr isotope ratios of the wine and the grapes. This suggests that the vinification process does not alter the overall Sr budget. Although the Sr isotope ratios of the grapes do not show a strong correlation with the bulk Sr isotope composition of the soil, they do correlate strongly with the Sr isotope composition contained in the labile fraction of the soil. This indicates that the labile fraction of the soil represents the Sr reservoir available to the plant during its growth. This study demonstrates that the Sr isotope approach can be used as a viable tool in forensic science for investigating the provenance of commercial wines.

  9. Strontium isotope characterization of wines from Quebec, Canada.

    Science.gov (United States)

    Vinciguerra, Victor; Stevenson, Ross; Pedneault, Karine; Poirier, André; Hélie, Jean-François; Widory, David

    2016-11-01

    The (87)Sr/(86)Sr isotope ratios were measured on grape, wine and soil samples collected in 13 commercial vineyards located in three major wine producing areas of Quebec (Canada). The soils yield Sr isotope ratios that are intimately related to the local geology and unambiguously discriminate the different producing areas. A strong relationship exists between the (87)Sr/(86)Sr isotope ratios of the wine and the grapes. This suggests that the vinification process does not alter the overall Sr budget. Although the Sr isotope ratios of the grapes do not show a strong correlation with the bulk Sr isotope composition of the soil, they do correlate strongly with the Sr isotope composition contained in the labile fraction of the soil. This indicates that the labile fraction of the soil represents the Sr reservoir available to the plant during its growth. This study demonstrates that the Sr isotope approach can be used as a viable tool in forensic science for investigating the provenance of commercial wines. PMID:27211629

  10. Automated Sample Preparation for Radiogenic and Non-Traditional Metal Isotopes: Removing an Analytical Barrier for High Sample Throughput

    Science.gov (United States)

    Field, M. Paul; Romaniello, Stephen; Gordon, Gwyneth W.; Anbar, Ariel D.; Herrmann, Achim; Martinez-Boti, Miguel A.; Anagnostou, Eleni; Foster, Gavin L.

    2014-05-01

    MC-ICP-MS has dramatically improved the analytical throughput for high-precision radiogenic and non-traditional isotope ratio measurements, compared to TIMS. The generation of large data sets, however, remains hampered by tedious manual drip chromatography required for sample purification. A new, automated chromatography system reduces the laboratory bottle neck and expands the utility of high-precision isotope analyses in applications where large data sets are required: geochemistry, forensic anthropology, nuclear forensics, medical research and food authentication. We have developed protocols to automate ion exchange purification for several isotopic systems (B, Ca, Fe, Cu, Zn, Sr, Cd, Pb and U) using the new prepFAST-MC™ (ESI, Nebraska, Omaha). The system is not only inert (all-flouropolymer flow paths), but is also very flexible and can easily facilitate different resins, samples, and reagent types. When programmed, precise and accurate user defined volumes and flow rates are implemented to automatically load samples, wash the column, condition the column and elute fractions. Unattended, the automated, low-pressure ion exchange chromatography system can process up to 60 samples overnight. Excellent reproducibility, reliability, recovery, with low blank and carry over for samples in a variety of different matrices, have been demonstrated to give accurate and precise isotopic ratios within analytical error for several isotopic systems (B, Ca, Fe, Cu, Zn, Sr, Cd, Pb and U). This illustrates the potential of the new prepFAST-MC™ (ESI, Nebraska, Omaha) as a powerful tool in radiogenic and non-traditional isotope research.

  11. Experiences with the determination of Sr-89 and Sr-90 using fast methods

    International Nuclear Information System (INIS)

    Quick methods of the measurement of 89Sr and 90Sr have a great importance in the supervision of the environmental radioactivity. It is necessary to receive in short time dependable analytical data to be able to carry out suitable assessments or to give recommendations. The aim of the investigations was to be guaranteed the demands for these methods (test preparation, measurement and evaluation). The use of the solid phase extraction by means of commercial Sr Resin trademark columns (4.4' (5')-Di-tert-butylcyclohexanol-18-kronen-6-aether) (Triskem) to the radiochemical separation of the Sr isotopes was suitable. The measurements occurred to the FHT 770 T12 - Multi Low Level Alpha/Beta Sample Counter (Thermo Scientific). The results contain the summary activities of all available Sr isotopes, as for example 89Sr and 90Sr. The calculations of the single activities occur about the mathematical algorithm of the linear development on the basis of the works of G. Kanisch. The first results show, this method is suitable for the analysis of 89Sr and 90Sr and is used therefore in future in Thuringia.

  12. Extraction chromatographic separation of Sr, Pu and Am in environmental samples

    Energy Technology Data Exchange (ETDEWEB)

    Sidhu, Rajdeep

    2004-04-01

    An accurate determination of radionuclides from various sources in the environment is essential for assessment of the potential hazards and suitable countermeasures both in case of an authorised release, accidents and routine surveillance. Due to the short range of alpha and beta radiation, the accurate determination of pure alpha and beta emitters must always include radiochemical separations to separate the analytes from the matrix and from other interfering stable and radioactive nuclides. Hence, the procedures used for their determination are usually tedious and involve several preconcentration and separation steps. This work deals with the determination of {sup 90}Sr, {sup 241}Am, {sup 238}Pu, {sup 239,240}Pu and {sup 244}Cm, whic some of the most important artificial radionuclides. Due to either absence or low yield of gamma radiation, a secure determination of low concentrations of all these nuclides requires a dedicated chemistry. Selective extraction chromatographic resins (TRU- and Sr-Resin) have been utilised to develop new procedures for the analyses of Pu, Am and Cm isotopes in seawater and both these and {sup 90}Sr in soil, sediment, urine and low-level liquid radioactive effluents. The proposed method for the analyses of Pu and Am in seawater offers a quick and secure mode for the determination of these radionuclides in marine waters. Combined pre-concentration of actinides and strontium (oxalate or phosphate precipitation) followed by dual column separation on TRU- and Sr-Resin significantly reduces the through put time and costs compared to traditional ion exchange and precipitation methods. The greatest gain in productivity and environmental friendliness is achieved in Sr separations using Sr-Resin instead of precipitations involving fuming nitric acid and oxalate, hydroxide, chromate and carbonate precipitations. (author)

  13. Petrogenesis of syntectonic granites emplaced at the transition from thrusting to transcurrent tectonics in post-collisional setting: Whole-rock and Sr-Nd-Pb isotope geochemistry in the Neoproterozoic Quatro Ilhas and Mariscal Granites, Southern Brazil

    Science.gov (United States)

    Florisbal, Luana Moreira; Bitencourt, Maria de Fátima; Janasi, Valdecir de Assis; Nardi, Lauro Valentim Stoll; Heaman, Larry M.

    2012-11-01

    The Neoproterozoic post-collisional period in southern Brazil (650-580 Ma) is characterized by substantial volumes of magma emplaced along the active shear zones that compose the Southern Brazilian Shear Belt. The early-phase syntectonic magmatism (630-610 Ma) is represented by the porphyritic, high-K, metaluminous to peraluminous Quatro Ilhas Granitoids and the younger heterogranular, slightly peraluminous Mariscal Granite. Quatro Ilhas Granitoids include three main petrographic varieties (muscovite-biotite granodiorite — mbg; biotite monzogranite — bmz; and leucogranite — lcg) that, although sharing some significant geochemical characteristics, are not strictly comagmatic, as shown by chemical and Sr-Nd-Pb isotope data. The most primitive muscovite-biotite granodiorite was produced by contamination of more mafic melts (possibly with some mantle component) with peraluminous crustal melts; the biotite monzogranite, although more felsic, has higher Ca, MgO, TiO2 and Ba, and lower K2O, FeOt, Sr and Rb contents, possibly reflecting some mixing with coeval mafic magmas of tholeiitic affinity; the leucogranite may be derived from pure crustal melts. The Mariscal Granite is formed by two main granite types which occur intimately associated in the same pluton, one with higher K (5-6.5 wt.% K2O) high Rb and lower CaO, Na2O, Ba and Zr as compared to the other (3-5 wt.% of K2O). The two Mariscal Granite varieties have compositional correspondence with fine-grained granites (fgg) that occur as tabular bodies which intruded the Quatro Ilhas Granoitoids before they were fully crystallized, and are inferred to correspond to the Mariscal Granite feeders, an interpretation that is reinforced by similar U-Pb zircon crystallization ages. The initial evolution of the post-collisional magmatism, marked by the emplacement of the Quatro Ilhas Granitoids varieties, activated sources that produced mantle and crustal magmas whose emplacement was controlled both by flat-lying and

  14. Geochemistry, zircon U-Pb ages and Sr-Nd-Hf isotopes of an Ordovician appinitic pluton in the East Kunlun orogen: New evidence for Proto-Tethyan subduction

    Science.gov (United States)

    Xiong, Fuhao; Ma, Changqian; Wu, Liang; Jiang, Hong'an; Liu, Bin

    2015-11-01

    Appinite is commonly derived from a mantle source in subduction zones and thus holds a key to constrain the tectonic evolution of ancient orogens. This study presents chronological, mineralogical and geochemical data for one appinitic pluton from the south Tethyan suture zone in the East Kunlun orogen, Northern Tibetan Plateau. The pluton is predominantly composed of hornblende-rich mafic appinites, with minor amounts of granodiorite. Zircon U-Pb age of the granodiorite (466 Ma) is identical to the mafic appinites (447-450 Ma). The mafic appinites are commonly hornblende diorites, which comprise large amounts of magnesio-hornblende [Mg/(Fe + Mg) = 0.61-0.68] and andesine (An43-54). The hornblende diorites have low contents of SiO2 (48.62-54.95 wt.%), high contents of total FeO (7.90-12.84 wt.%) and MgO (4.32-11.89 wt.%) and moderate values of Mg# [Mg# = molar 100 ∗ Mg/(Mg + Fe); 49-69]. Their geochemistry displays: slight enrichment of light rare earth elements ((La/Yb)N = 1.89-6.84) and flat heavy rare earth elements ((Ga/Yb)N = 1.49-2.22); enrichment in large ion lithophile elements and depletion in high field strength elements; less-enriched isotopic compositions with initial 87Sr/86Sr ratios of 0.70536-0.70617, εNd(t) of 0.79-3.02 and zircon εHf(t) of 8.73-12.82. The associated granodiorites comprise plagioclase (45-50 vol.%, An = 26-39), quartz (15-20 vol.%), K-feldspar (5-10 vol.%), ferrohornblende [2-5 vol.%, (Mg/(Fe + Mg) = 0.45-0.49] and epidote (1-5 vol.%). The epidotes have pistacite components ranging from 23 to 28. The granodiorites exhibit calc-alkaline character, and have rare earth and trace element patterns similar to the hornblende diorites. The geochemical compositions and simulations suggest that the parental magma of the mafic appinites was generated by partial melting of one depleted mantle source which was metasomatised by subducted sediment-derived felsic melts (ca. 20-25%). Fractional crystallization of clinopyroxene, hornblende

  15. Preliminary Sr-Nd isotope study of the Hadong-Sanchung anorthositic rocks in Korea: Implication for their origin and for the Precambrian tectonics%韩国Hadong-Sanchung地区斜长岩Sr-Nd同位素初步研究--成因和前寒武纪构造意义

    Institute of Scientific and Technical Information of China (English)

    郑址昆

    2005-01-01

    斜长岩呈长条带出露于朝鲜半岛南部,侵入到年代约为2.0 Ga的Yeongnam前寒武纪基底岩石中,虽然岩石类型简单(斜长岩和辉长岩质斜长岩),但可以同世界已知块状类型斜长岩相对比.这些斜长岩具有几个重要的差别,例如呈层状构造,镁铁相成分是角闪石而不是辉石,并且不具斜方辉石巨晶.应用Rb-Sr和Sm-Nd同位素系统研究这些岩石的年龄和成因,测定出一种页理化辉长岩质斜长岩矿物的Sm-Nd等时线年龄为1 678±90 Ma,推断其为侵位年龄,因为中生代绿岩相变质期间这些岩石的Sm-Nd同位素体系呈封闭状态.这一年龄和过去曾报道的元古宙块状斜长岩的年龄范围(1.1~1.7 Ga)相吻合.认为斜长岩成因可以用所谓元古宙斜长岩事件来解释.斜长岩的岩浆活动对朝鲜半岛南部前寒武纪基底岩石的构造历史有重要意义.全岩εNd(t)值范围-1.6~-5.2,而87Sr/86Sr初始值变化于0.704~0.706之间,据此可解释地幔成因的斜长岩岩浆是在其结晶作用期间吸收了地壳物质的结果.然而不能排除是下地壳源的可能性.%The anorthositic rocks in southern part of Korean peninsula occur as a long belt, intruding the ca. 2.0 Ga old Precambrianbasement rocks of the Yeongnam massif. Although they have simple rock types (anorthosite and gabbroic anorthosite) comparable towell known massif-type anorthosites worldwide, they possess several important differences such as layered structure, amphibole ratherthan pyroxene as a mafic phase, and no orthopyroxene megacrysts. The age of intrusion was not available previously. We have appliedRb-Sr and Sm-Nd isotope systematics to investigate the age and origin of these rocks. One foliated gabbroic anorthosite defines a Sm-Nd mineral isochron age of 1678 ± 90 Ma. This age is tentatively interpreted as the emplacement age because of apparently closed-sys-tem behavior of Sm-Nd system in these rocks during greenschist

  16. GEOCHRONOMETRY ISOTOPE GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2004-01-01

    <正>20040631 Chen Jiangfeng (School of Earth and Space Sciences, University of Science and Technology of China, Hefei, Anhui) ; Xie Zhi Relationships Between Rb-Sr, Ar - Ar Geochronometers and Oxygen Isotopic Equilibrium of Intrusions from Eastern Anhui Province, China (Geological Journal of China Universities, ISSN 1006 - 7493, CN 32 -

  17. Isotope hydrogeochemistry in exploration for buried and blind mineralisation

    International Nuclear Information System (INIS)

    Detection of concealed orebodies using the isotopic composition of Pb, S and Sr in groundwaters has been tested in several base metal exploration prospects in Australia Lead and S isotopes provide easily interpretable direct ore indicators, Pb isotopes provide a local target whereas S isotopes have application in regional target definition with isotopically-defined ore signatures recognisable for up to several kilometres from known mineralisation High 87Sr/86Sr ratios in groundwaters, apparently reflecting alteration related to mineralisation, also appear to provide a useful regional exploration tool

  18. Zircon U-Pb ages and Sr-Nd-Hf isotopes of the highly fractionated granite with tetrad REE patterns in the Shamai tungsten deposit in eastern Inner Mongolia, China: Implications for the timing of mineralization and ore genesis

    Science.gov (United States)

    Jiang, Si-Hong; Bagas, Leon; Hu, Peng; Han, Ning; Chen, Chun-Liang; Liu, Yuan; Kang, Huan

    2016-09-01

    The Shamai tungsten deposit is located in the eastern part of the Central Asian Orogenic Belt (CAOB). Tungsten mineralization is closely related to the emplacement of fine- to medium-grained biotite monzogranite (G1) and porphyritic biotite monzogranite (G2) in the Shamai Granite. NW-trending joints and faults host orebodies in the Shamai Granite and Devonian hornfels. The mineralization is characterized by a basal veinlet zone progressing upwards to a thick vein zone followed by a mixed zone, a veinlet zone, and a thread vein zone at the top. The ore-related alteration typically consists of muscovite, greisen, and hornfels. In order to constrain the timing of the Shamai mineralization and discuss the ore genesis, muscovite Ar-Ar, molybdenite Re-Os, and zircon U-Pb geochronological, geochemical, and Sr-Nd-Hf isotopic studies were completed on the deposit. The U-Pb zircon dating yielded weighted mean ages of 153 ± 1 Ma for G1 and 146 ± 1 Ma for G2. Muscovite from a wolframite-bearing quartz vein yielded an Ar-Ar plateau age of 140 ± 1 Ma, whereas two molybdenite samples yielded identical Re-Os model ages of 137 ± 2 Ma. These two ages are younger than the two monzogranites, suggesting a prolonged magmatic-hydrothermal interaction during tungsten mineralization. Major and trace element geochemistry shows that both G1 and G2 are characterized by high SiO2 and K2O contents, high A/CNK values (1.08-1.40), a spectacular tetrad effect in their REE distribution patterns, and non-CHARAC (charge-and-radius-controlled) trace element behavior. This suggests that both G1 and G2 are highly differentiated peraluminous rocks with strong hydrothermal interaction. The Nd-Hf isotope data for the Shamai Granite (εNd(t) between - 1.9 and + 7.4, ɛHf(t) from 5.2 to 12.8) are largely compatible with the general scenario for much of the Phanerozoic granite emplaced in the CAOB. It is here suggested that the Shamai Granite originated from partial melting of a juvenile lower crust with

  19. 华北克拉通北缘东段海沟岩体的锆石U-Pb年龄、Sr-Nd-Hf同位素组成及其动力学背景%Zircon U-Pb ages and Sr-Nd-Hf isotopic composition of the Haigou granitoids at the northeastern margin of North China Craton: Implications for geodynamic setting

    Institute of Scientific and Technical Information of China (English)

    张松; 王永彬; 褚少雄

    2012-01-01

    海沟岩体位于华北克拉通北缘东段,由二长岩和二长花岗岩组成.本文对该岩体主微量元素、Sr-Nd-Hf同位素和锆石的U-Pb年龄进行了系统研究.高精度锆石U-Pb年龄测试结果表明,二长岩和二长花岗岩形成的精确年龄分别为322.9±3.4Ma和320.3±3.5 Ma,为海西期构造-岩浆活动产物.海沟岩体为准铝质-弱过铝质的Ⅰ型花岗岩,其K2O/Na2O比值介于0.51 ~0.93之间,A/CNK介于0.87 ~0.94之间.微量元素方面表现为轻稀土富集、轻重稀土分馏明显、弱铕正异常、大离子亲石元素(如Rb、Ba、K)富集,以及高场强元素(如Nb、Ta、Ti、P)相对亏损等.锶同位素初始比值为(87Sr/86Sr)i=0.7054~0.7059,εNd(t)=- 10.4~ -8.6,亏损地幔的钕模式年龄分别介于1.84 ~ 1.99Ga和1.84~ 1.93Ga之间.二长岩和二长花岗岩锆石的εHf(t)变化范围分别为-7.6~ -0.8和-11.5~ -5.4,对应的两阶段Hf模式年龄分别为1.39 ~1.81Ga和1.67 ~2.06Ga.同位素特征表明两者可能来自中元古代和古元古代的下地壳物质的部分熔融,并可能有较多地幔物质的加入.根据其形成时代、岩石地球化学、同位素特征以及区域地质演化史,认为海沟岩体的形成可能与古生代古亚洲洋消减作用密切相关.%The Haigou granitoids, located in the northeastern margin of the North China Craton, consists of monzonite and monzogranite.. This study presents zircon U-Pb age, geochemical compositions and Sr-Nd-Hf isotopes of the Haigou granitoids, to discuss the origin and tectonic setting of the magmas. The zircon U-Pb dating for the monzonite and monzogranite yields 322. 9 ± 3. 4Ma and 320. 3 ±3. 5Ma respectively, indicating the magmas emplaced during the Hercynian Period. Petrochemical data indicate that they belong to calc-alkaline I-type granitoids with metaluminous affinity. They have similar geochemical features such as K2O/Na2O ratios being between 0. 51 and 0. 93 , A/CNK ranging from 0

  20. Age of nephrite-bearing dikes of the Uzunkyr Belt (South Urals): Local U-Pb isotope analysis of zircon and Sr-Nd isotope data of rock-forming minerals

    Science.gov (United States)

    Arkhireev, I. E.; Makagonov, E. P.; Belyatskii, B. V.; Maslennikov, V. V.

    2012-01-01

    Through local U-Pb isotope analysis of zircon and Sir-Need data on rock-forming minerals, the age of nephrite-bearing monzonite-diorite dikes of the Uzunkyr Belt has been determined. The derived datings coincide with known geological events that took place in the Phanerozoic on the territory of the South Urals. Xenogenic zircons prove the participation of the Upper Ordovician units in the tectonic structure of the studied area. Devonian zircons are associated with assimilation of subvolcanic rocks which are middle and basic in composition and whose formation time correlates with the appearance of the subduction zone with the Magnitogorsk island arc above it. Early Carboniferous datings indicate the relationship between dike formation and formation of the continental arc-shaped structure to which the Syrostan massif (monzodiorite-granite formation) belongs. The age range of the Uzunkyr nephrite-bearing dikes coincides with that of intrusives (350-336 Ma) of the Magnitogorsk Belt, where formation of gabbro series was also changed by formation of subalkali and alkali igneous rocks. According to the analogous data on zircon datings from metamorphic rocks of the Il'menogorskii Complex, the given territory later evolved as a whole.

  1. Petrogenesis and tectonic settings of volcanic rocks of the Ashele Cu-Zn deposit in southern Altay, Xinjiang, Northwest China: Insights from zircon U-Pb geochronology, geochemistry and Sr-Nd isotopes

    Science.gov (United States)

    Wu, Yufeng; Yang, Fuquan; Liu, Feng; Geng, Xinxia; Li, Qiang; Zheng, Jiahao

    2015-11-01

    The Early-Mid-Devonian Ashele Formation of the southern margin of the Chinese Altay hosts the Ashele Cu-Zn volcanogenic massive sulfide (VMS) deposit and consists of intercalated volcanic and sedimentary rocks that have experienced regional greenschist-facies metamorphism. We studied the petrography, zircon U-Pb geochronology, geochemistry, and Sr-Nd isotopes of dacites and basalts in order to understand the petrogenesis of these rocks and the regional tectonic evolution. Two dacites yielded LA-MC-ICP-MS zircon U-Pb ages of 402 ± 6 Ma and 403 ± 2 Ma. The dacites are calc-alkaline, and characterized by high Na2O/K2O ratios (3.6-9.3), and high Mg# values (47-63), enrichment in large ion lithophile elements (LILE) and light rare earth elements (LREE), depletion in Nb, Ta, Ti, and P, and relatively positive εNd(t) values (+3.6 to +7.5), collectively suggesting a sanukitic magma affinity. The variations in the major and trace elements of the dacites indicate that Fe-Ti oxide, plagioclase, and apatite were fractionated during their petrogenesis. The basalts are tholeiitic, and are characterized by high Mg# values (66-73), and negative Nb and Ta anomalies. The geochemical characteristics of the basalts are similar to those of N-MORB. Those characteristics together with the positive εNd(t) values (+6.8 to +9.2) of the basalts, indicate that the precursor magma was derived mainly from an N-MORB-type depleted asthenospheric mantle in an island arc setting. The geochemical similarities between the basalts and dacites indicate that they both originated from a similar depleted mantle source via partial melting under different magmatic conditions in each case, possibly related to ridge subduction.

  2. The applicability of an 87Sr/86Sr river isoscape to fish ecological questions in the Danube catchment

    Science.gov (United States)

    Zitek, A.; Irrgeher, J.; Sailer, K.; Trautwein, C.; Waidbacher, H.; Prohaska, T.

    2012-04-01

    Isoscapes are spatial maps of the distribution of isotopes on Earth. As a basis for ecological studies such as long distance migrations of animals or for determining the origin of food these tools are increasingly being developed, until now - mainly for terrestrial systems. In contrast, in case of aquatic systems only few maps were established up to now. As far as variation in the isotopic distribution in a studied area exists, the isotopic composition bears the potential to be used as natural tracer e.g. for ecological questions or food authentication. Above all the 87Sr/86Sr ratio taken up from the environment by organisms without any significant fractionation is known to provide a direct link to geologically distinct regions. Within the 'IsoMark' project (www.isomark.at), a database ('Isoscape Austria') containing all available spatially explicit isotope data (terrestrial and aquatic) with a focus on isotope distributions in Austrian rivers is being developed. Water samples from different rivers, mainly along the Danube in Austria, were collected and analyzed for their elemental and Sr isotopic composition. Analyses of water samples yielded several 'Isozones' along the Austrian part of the Danube, indicating diverse geology in these river catchments. Studying migration phenomena of fish using natural isotopic marks in hard parts is especially possible between these 'Isozones'. In geologically similar regions with little differences, element distributions or artificial marking methods (tagging, spiking) can serve as additional means. A significant positive relationship between the 87Sr/86Sr ratio in river water and the proportion of siliceous geological formations in the catchment was found on a national and European level. These analyses proved the possibility to predict the 87Sr/86Sr ratios in river catchments all over Europe. This relationship allows for an estimation of the applicability of the 87Sr/86Sr ratio for fish ecological questions on a European scale

  3. Study on Petrology, Geochemistry and Os-Nd-Sr Isotopes of Jinan Gabbro in Luxi Block%鲁西地块济南辉长岩岩石学、地球化学和Os-Nd-Sr同位素研究

    Institute of Scientific and Technical Information of China (English)

    高林; 陈斌

    2013-01-01

    Petrology,geochemistry and Os-Nd-Sr isotopes of Jinan gabbro in Luxi block of eastern block of North China Craton were studied in detail,and diagenetic process,characteristic of mantle source and the role of crustal contamination on evolution process of mantle-derived magma were discussed.Jinan gabbro was rich in LREE and LILE,depleted in HREE and HFSE;radiogenic Os isotopic composition was high for Jinan gabbro,the characteristic of Sr-Nd isotopic composition was EM1-like.The results of petrology and element geochemistry suggested a significant fractional crystallization of olivine +pyroxene+ plagioclase in forming the mafic pluton.The characteristics of petrology,geochemistry and Os-Nd-Sr isotopes showed that the parental magmas of Jinan gabbro was hydrous magma system,which originated from an old enriched lithospheric mantle.High radiogenic initial Os isotopic composition and inverse relationship between value of εNd and ratio of initial Sr isotopic compositions of the mafic pluton suggested that parental magmas were contaminated by Precambrian mafic lower crust during magma emplacement at a deep crustal level.%对华北克拉通东部陆块鲁西地块济南辉长岩进行了详细的岩石学、地球化学和Os-Nd-Sr同位素研究,探讨了该岩体的成岩过程、地幔源区特征以及地壳混染在幔源岩浆演化过程中的作用.济南辉长岩在地球化学上富集轻稀土元素和大离子亲石元素,亏损重稀土元素以及高场强元素;它们具有高放射性成因的Os同位素组成,Sr-Nd同位素组成具有EM1型特征.岩石学和元素地球化学研究表明,该岩体在成岩过程中经历了显著的橄榄岩+辉石+斜长石的分离结晶.岩石学、地球化学和Sr-Nd同位素特征研究表明,济南辉长岩的母岩浆应该是含水的岩浆体系,且起源于一个古老的富集岩石圈地幔.岩体所具有的高放射性成因的初始Os同位素组成以及呈反相关关系的εNd(t)值和初始Sr同位

  4. Geographical origin of Amazonian freshwater fishes fingerprinted by ⁸⁷Sr/⁸⁶Sr ratios on fish otoliths and scales.

    Science.gov (United States)

    Pouilly, Marc; Point, David; Sondag, Francis; Henry, Manuel; Santos, Roberto V

    2014-08-19

    Calcified structures such as otoliths and scales grow continuously throughout the lifetime of fishes. The geochemical variations present in these biogenic structures are particularly relevant for studying fish migration and origin. In order to investigate the potential of the (87)Sr/(86)Sr ratio as a precise biogeochemical tag in Amazonian fishes, we compared this ratio between the water and fish otoliths and scales of two commercial fish species, Hoplias malabaricus and Schizodon fasciatus, from three major drainage basins of the Amazon: the Madeira, Solimões, and Tapajós rivers, displaying contrasted (87)Sr/(86)Sr ratios. A comparison of the (87)Sr/(86)Sr ratios between the otoliths and scales of the same individuals revealed similar values and were very close to the Sr isotopic composition of the local river where they were captured. This indicates, first, the absence of Sr isotopic fractionation during biological uptake and incorporation into calcified structures and, second, that scales may represent an interesting nonlethal alternative for (87)Sr/(86)Sr ratio measurements in comparison to otoliths. Considering the wide range of (87)Sr/(86)Sr variations that exist across Amazonian rivers, we used variations of (87)Sr/(86)Sr to discriminate fish origin at the basin level, as well as at the sub-basin level between the river and savannah lakes of the Beni River (Madeira basin).

  5. LA-ICP MS zircon dating, whole-rock and Sr-Nd-Pb-O isotope geochemistry of the Camiboğazı pluton, Eastern Pontides, NE Turkey: Implications for lithospheric mantle and lower crustal sources in arc-related I-type magmatism

    Science.gov (United States)

    Kaygusuz, Abdullah; Arslan, Mehmet; Siebel, Wolfgang; Sipahi, Ferkan; İlbeyli, Nurdane; Temizel, İrfan

    2014-04-01

    Late Cretaceous I-type plutons are widespread in the Eastern Pontides, NE Turkey. The studied Camiboğazı pluton is a composite pluton consisting of diorite, tonalite, monzodiorite, monzonite, quartz monzonite, granite, and mafic microgranular enclaves (MMEs). Laser ablation ICP-MS U-Pb dating of zircon yielded crystallization ages of 76.21 ± 0.79 Ma, 75.65 ± 0.50 Ma, 75.04 ± 0.83 Ma, and 74.73 ± 0.86 Ma for diorite, monzodiorite, monzonite, and granite, respectively. The rocks of the pluton have I-type, high-K to shoshonitic and metaluminous character, displaying whole-rock geochemical features of arc-related granites. They are enriched in large-ion lithophile and light rare-earth elements, and depleted in high-field-strength elements. Major element variations can be attributed to fractionation of plagioclase, clinopyroxene, hornblende, and Fe-Ti oxides. The rocks show considerable variation in 87Sr/86Sr(i) (0.70498 to 0.70622), ɛNd(i) (- 2.79 to - 0.36), δ18O values (+ 6.3 to + 11.4) and Nd model ages (TDM) (0.81 Ga to 1.26 Ga). Besides, they have (206Pb/204Pb) = 18.44-19.09, (207Pb/204Pb) = 15.64-15.69, and (208Pb/204Pb) = 38.37-38.89. Although isotope signatures of the mafic microgranular enclaves (MMEs) (87Sr/86Sr(i) = 0.70551 to 0.70622; ɛNd(i) = - 2.9 to - 1.23; δ18O = + 8.3 to + 9.7) are largely similar to the host rocks, MMEs are characterized by relatively high Mg-numbers (32-36), low contents of SiO2 (52-56 wt.%) and low ASI (0.7-0.9). Estimated crystallization temperatures for the rocks of the pluton range from 735 ± 58 °C to 844 ± 24 °C and a shallow intrusion depth (< 10 km) is estimated from Al-in-hornblende thermobarometry. Whole-rock geochemical and isotopic data suggest magma generation by dehydration melting of an amphibolite-type lower crustal component with additional input of a subcontinental lithospheric mantle component. Furthermore, Sr-Nd isotope mixing model reveals ~ 30% to 40% lower crustal magma contribution to the mantle

  6. Geochemistry and Sr- Nd Isotopic Characteristics of the Carboniferous Volcanic Rocks from the Eastern Tianshan Suture Zone and Tectonic Implications%东天山板块缝合带石炭纪火山岩地球化学和Sr-Nd同位素特征及其大地构造意义

    Institute of Scientific and Technical Information of China (English)

    曹锐; 木合塔尔·扎日; 陈斌; 李德威; 曹福根; 刘德民

    2012-01-01

    对东天山沿康古尔塔格缝合带分布的企鹅山群和梧桐窝子组火山岩的地球化学特征及Rb - Sr和Sm - Nd同位素进行了系统研究.结果显示:企鹅山群火山岩富集LREE,Eu异常变化较大(从明显负异常到微弱正异常),富集Sr、Ba和U等大离子亲石元素,相对亏损Nb、Zr、Ti等高场强元素,Sr - Nd同位素特征是Isr=0.703 97~0.704 26,εNd (t) =5.61~6.99,具有亏损地幔性质,表明其岩浆源区可能来自古生代期间被古亚洲洋俯冲板片释放的流体/熔体交代过的岩石圈地幔楔;梧桐窝子组玄武岩富集轻稀土元素(LREE)和大离子亲石元素,而高场强元素没有明显负异常,样品的εNd值都在9以上,Isr (330 Ma)为0.704 71~0.705 33,表明梧桐窝子组玄武岩可能来自亏损的软流圈地幔的部分熔融.企鹅山群和梧桐窝子组火山岩在Zr - Zr/Y判别图解中分别落在岛弧拉斑玄武岩(IAB)和板内玄武岩(WPB)范围内,表明企鹅山群可能为准噶尔洋盆向南俯冲形成的石炭纪岛弧火山岩,而梧桐窝子组火山岩可能形成于在弧后盆地的基础上拉张为裂陷槽的伸展环境.%Geochemistry, Rb - Sr and Sm - Nd isotopic compositions of the volcanic rocks, from the Qi'eshan Group and Wutongwozi Formation in the eastern Tianshan plate suture zone have been studied in this paper. The basalt from the Qi' eshan Group is highly enriched in light rare earth elements (LREEs) and large ion lithophile elements (LILEs) such as Sr, Ba and U, and depleted in high field strength elements (Nb, Ti and Zr) , with variable Eu anomalies (varying from significant negative Eu anomalies to minor positive Eu anomalies) in the chondrite-normalized REE patterns. It is charactered by isotopic signatures of depleted mantle source, with εNd(t) = 5. 61 -6. 99, and Isr(330 Ma)=0. 703 97 -0. 704 26. All these geochemical characteristics suggest that the basalt in Qi'eshan Group probably was derived from the lithospheric

  7. 黄河下游地区河水主要离子和锶同位素的地球化学特征%GEOCHEMISTRY OF THE MAIN IONS AND Sr ISOTOPIC COMPOSITION IN THE LOWER REACH OF THE YELLOW RIVER, NORTH CHINA

    Institute of Scientific and Technical Information of China (English)

    王兵; 李心清; 袁洪林; 周会; 赵彦龙

    2009-01-01

    The Yellow River is one of the largest rivers in China, and plays significant role in the development of the society and economy, as well as the ecosystem health in northern China. Major ions and the strontium isotopic composition are important geochemical characters of the water body, and provide insight into the regional hydrogeochemistry, rock weathering rates in drainage basins, and anthropogenic influences on the river. This study determined ~(87)Sr/~(86)Sr ratios and concentration of Sr and major anions and cations in 16 water samples from the lower reach of the Yellow River. Ca~(2+) , Na~+ , HCO_3~- and SO_4~(2-) are the dominant ions. The concentration of the ions accounts for more than 75% in the respective categories, and differ significantly between the tributary and the mainstream. Sources of SO_4~(2-), NO_3~- and Cl~- are homogenized in the mainstream, while clearly different in the tributaries. The lower section of the reach is higher in Sr concentration while lower in the Srisotope composition, which range from 0.0429mg ·l~(-1) to 0.936mg ·l~(-1) and from 0.70986 to 0.71139, respectively. The isotopic composition in the estuary is similar to that of the sea water, suggesting that the isotopic geochemistry has been under the control of the sea. The research of major elements, the Sr concentration and ~(87)Sr/~(86)Sr ratios show that the weathering of carbonates and evaporates in the drainage basins are responsible for the high water Sr concentrations. According to the balance equation of Sr, the Sr in river water is derived from two end members, that is, the ratio of ~(87)Sr/~(86)Sr from atmosphere precipitation is about 30% and from rock weathering is about 70%.%对黄河下游地区河水主要阴阳离子、锶元素及其同位素组成进行了分析.结果发现其水化学组成主要以Ca~(2+),Na~+,HCO_3~-和SO_4~(2-)离子为主,分别占阴阳离子组成的75%以上.干流与支流间在化学组成上存在

  8. Combined marine δ88/86Sr and 87Sr/86Sr record supports global anoxia as a cause for P/T mass extinction

    Science.gov (United States)

    Vollstaedt, H.; Eisenhauer, A.; Boehm, F.; Fietzke, J.; Krabbenhöft, A.; Liebetrau, V.; Wallmann, K. J.; Farkas, J.

    2011-12-01

    The biggest mass extinction within the Phanerozoic Eon occurred at the Permian/Triassic (P/T) boundary and is characterized by up to 96% loss in species accompanied with the demise of the Paleozoic faunal community. Recently, five major mechanisms are consulted to explain the mass extinction in terrestrial and marine environment. However, a geochemical quantification of carbonate burial rates during this biotic turnover is still remaining. By extending the conventional radiogenic isotope system by a simultaneous measurement of radiogenic and stable strontium (Sr) isotopes (δ88/86Sr) we are able to add new constraints to the seawater chemistry including quantitative information about the Sr output flux of the ocean, mainly represented by marine carbonates. Consequently, variations in δ88/86Sr becoming a suitable tool to investigate in the global carbonate budget in earth's history including the biotic turnover of calcifying organisms at stratigraphic boundaries which are expected to have a large influence on Sr geochemistry and isotope composition of seawater. In order to examine variations in the marine Sr isotope composition through Earth's history paired 88Sr/86Sr-87Sr/86Sr-ratios of 104 Phanerozoic brachiopods, belemnites and carbonate matrix samples are determined. Applying the fractionation factor of our carbonate recording phase we constructed a δ88/86Srseawater record. The most noteworthy observation is the occurrence of the two global extrema in δ88/86Sr values of the whole Phanerozoic within the last 20Ma years of the Paleozoic prior to the P/T boundary. This corresponds to an increase of δ88/86Srseawater of 0.000249 Ma-1 in the latest Permian indicating a strong disturbance in the Sr budget of the ocean. To interpret our observations and to compare them to existing scenarios for the P/T boundary we applied a one-box, isotope mass balance model of the oceanic Sr cycle connected to a mass balance model of Ca. Our results show a high strontium output

  9. 远源地下水入侵阿拉善高原沙漠:酸溶物 Sr 同位素证据%Invasion of Remote Groundwater into Deserts on the Alxa Plateau:Acid Soluble Sr Isotopic Evidence

    Institute of Scientific and Technical Information of China (English)

    潘耀东; 饶文波; 王啸

    2014-01-01

    选取北方西-东向气候剖面上物质组成相似的4个沙漠(塔克拉玛干、巴丹吉林、腾格里和毛乌素),测定其地表沙酸溶物87 Sr/86 Sr 比值(质量之比)及 Ca2+和 Sr2+质量比.结果表明,Ca2+和 Sr2+质量比相关性极好,在降雨量低的塔克拉玛干沙漠中最高,向东逐渐降低,在降雨量多的毛乌素沙漠中最低.降雨量是控制阳离子浓度变化的主导因素.酸溶物87 Sr/86 Sr 比值在4个沙漠中有不同于阳离子变化的区域特征.酸溶物87 Sr/86 Sr 比值在塔克拉玛干沙漠中低于0.7100,在巴丹吉林和腾格里沙漠中大于0.7112,而在毛乌素沙漠中介于0.7100~0.7112之间.塔克拉玛干和毛乌素沙漠地表沙酸溶物87 Sr/86 Sr 比值仅受气候变化的制约.巴丹吉林和腾格里沙漠除了受气候因素影响外还受其它因素的制约,远源地下水对巴丹吉林沙漠的影响为47%,对腾格里沙漠为44%,接近气候因素的影响.%87 Sr/ 86 Sr ratios and Ca2 + ,Sr2 + concentrations of acid soluble fractions of surface sands are measured for four deserts(Taklimakan,Badain Jaran,Tengger and Mu Us)with similar mineral and geochemical compositions in the W-E direction over North China. Ca2 + and Sr2 + concentrations have an excellent correlation,are the highest in the Taklimakan Desert with the low rainfall,decreasing eastwards,and the lowest in the Mu Us sandy land with the high rainfall. The rainfall is the main factor controlling cationic concentration. Acid soluble 87 Sr/ 86 Sr ratios have regional characteristics different from cationic change in the four deserts. Acid soluble 87 Sr/ 86 Sr ratios are low-er than 0. 71 for the Taklimakan desert,more than 0. 711 2 for the Badain Jaran and Tengger deserts,and between 0. 71 and 0. 711 2 in the Mu Us sandy land. Acid soluble 87 Sr/ 86 Sr ratios of surface sands in the Taklimakan desert and the Mu Us sandy land were only affected by climate factor. The Badain

  10. First evidence for expressive neoproterozoic intraplated mafic rocks and magma mixing in post-collisional A-PA type granites, Southern Brazil: Geochemistry and U-Pb (zircon), Nd-Sr-18O(zircon) isotope investigations

    International Nuclear Information System (INIS)

    Palermo Granite, formed between 595-585 Ma, is mainly constituted by medium to coarse grained, non deformed A-type amphibole-biotite and biotite monzo-syenogranites, and subordinately slightly peralkaline (PA-type) quartz-monzonites/quartz-syenites with sodic amphibole and pyroxene, intraplated alkaline mafic rocks and associated felsic and mafic hybrid granite rocks. The Rio Negro Granite, formed between 595-585, Ma is mainly constituted by mafic and felsic hybrid granite rocks and associated alkaline mafic rocks and non deformed A-type biotite monzo-syenogranites. The peralkaline rocks are absent in the Rio Negro Granite. The A-type monzo-syenogranites of Palermo and Rio Negro and, A-type leucogranodiorites of Agudos do Sul Granite are high silica (SiO2 70-80%), aluminous (meta-aluminous to slightly peraluminous) with low Sr, low Ba, high Rb content and high Ga, Zr, Hf, Nb and Y contents and, high LREE and HREE with high Eu negative anomalies. The slightly peralkaline quartz-monzonites/quartz-syenites (SiO2 = 60-65 %) of Palermo Granite presents very low Sr, low Ba, high Rb, very high Zr, Hf and Y, and LREE and HREE enrichment with high Eu negative anomalies. The alkaline mafic rocks emplaced within Palermo and Rio Negro Granites forms, by mixing with the adjacent A-type monzo to syenogranites, a great variety of mafic (hybrid monzodiorites/hybrid monzogabbros, hybrid quartz-monzodiorites to hybrid quartz-monzonitos) and felsic (hybrid quartz-monzodiorites, hybrid quartz-monzonitos to hybrid monzogranitos) hybrid rocks. The mafic and felsic hybrid rocks are mainly characterised by the presence of typical mixing textures such as, quartz-ocelli with or without interstitial perthite mantled by pyroxene, amphibole and biotite, chaotic acicular apatite, rounded and elliptical mafic (biotite, amphibole/pyroxene) concentrations. The mixing textures are absent in the alkaline mafic rocks. The lithochemical and 18O isotope investigations on these hybrid rocks and the mixing

  11. Isotope pattern deconvolution as rising tool for isotope tracer studies in environmental research

    Science.gov (United States)

    Irrgeher, Johanna; Zitek, Andreas; Prohaska, Thomas

    2014-05-01

    During the last decade stable isotope tracers have emerged as versatile tool in ecological research. Besides 'intrinsic' isotope tracers caused by the natural variation of isotopes, the intentional introduction of 'extrinsic' enriched stable isotope tracers into biological systems has gained significant interest. Hereby the induced change in the natural isotopic composition of an element allows amongst others for studying the fate and fluxes of metals, trace elements and species in organisms or provides an intrinsic marker or tag of particular biological samples. Due to the shoreless potential of this methodology, the number of publications dealing with applications of isotope (double) spikes as tracers to address research questions in 'real world systems' is constantly increasing. However, some isotope systems like the natural Sr isotopic system, although potentially very powerful for this type of application, are still rarely used, mainly because their adequate measurement/determination poses major analytical challenges; as e.g. Sr is available in significant amounts in natural samples. In addition, biological systems underlie complex processes such as metabolism, adsorption/desorption or oxidation/reduction. As a consequence, classic evaluation approaches such as the isotope dilution mass spectrometry equation are often not applicable because of the unknown amount of tracer finally present in the sample. Isotope pattern deconvolution (IPD), based on multiple linear regression, serves as simplified alternative data processing strategy to double spike isotope dilution calculations. The outstanding advantage of this mathematical tool lies in the possibility of deconvolving the isotope pattern in a spiked sample without knowing the quantities of enriched isotope tracer being incorporated into the natural sample matrix as well as the degree of impurities and species-interconversion (e.g. from sample preparation). Here, the potential of IPD for environmental tracer

  12. Analysis of coupled Sr/Ca and 87Sr/ 86Sr variations in enamel using laser-ablation tandem quadrupole-multicollector ICPMS

    Science.gov (United States)

    Balter, Vincent; Telouk, Philippe; Reynard, Bruno; Braga, José; Thackeray, Francis; Albarède, Francis

    2008-08-01

    We present in this study results obtained with a laser-ablation coupled with both a quadrupole and a multi-collector ICPMS. The simultaneous in situ Sr/Ca and 87Sr/ 86Sr measurements along growth profiles in enamel allows the concomitant diet and migration patterns in mammals to be reconstructed. Aliquots of the powdered international standard NIST "SRM1400 Bone Ash" with certified Sr and Ca contents, was sintered at high pressure and temperature and was adopted as the reference material for external reproducibility and calibration of the results. A total of 145 coupled elemental and isotopic measurements of herbivores enamel from the Kruger National Park, South Africa, gives intra-tooth Sr/Ca and 87Sr/ 86Sr variations that are well larger than external reproducibility. Sr/Ca profiles systematically decrease from the dentine-enamel junction to the outer enamel whereas 87Sr/ 86Sr profiles exhibit variable patterns. Using a simple geometric model of hypsodont teeth growth, we demonstrate that a continuous recording of the 87Sr/ 86Sr variations can be reconstructed in the tooth length axis. This suggests that the mobility of a mammal can be reconstructed over a period of more than a year with a resolution of a ten of days, by sampling enamel along growth profiles. Our geometric model of hypsodont teeth growth predicts that an optimal distance between two successive profiles is equal to the enamel thickness. However, this model does not apply to the Sr/Ca signal which is likely to be altered during the enamel maturation stage due to differential maturation processes along enamel thickness. Here, the observed constant decreases of the Sr/Ca ratios in the ungulates of Kruger National Park suggests that they did not changed of diet, while some of them were migrating.

  13. ID-TIMS 准确测定国际关键比对大米粉中痕量镉%Accurate Determination of Trace Amount of Cadmium in Rice for International Key Comparison by Isotope Dilution Thermal Ionization Mass Spectrometry

    Institute of Scientific and Technical Information of China (English)

    王军; 赵墨田; 逯海

    2005-01-01

    The method of isotope dilution thermal ionization mass spectrometry able to trace to SI was developed to accurately measure trace amount of cadmium in the rice powder sample from CCQM-K24 international key comparison organized by CCQM(Comité Consultatif pour la Quantité de Matière, Paris). By comparison with our previous work, there was much improvement in aspects of digestion of the rice powder sample, separation of cadmium from the sample and dry-mass correction. As a result, the blank of this procedure was reduced and the measurement precisions of isotopic ratios of cadmium were increased. In addition, the uncertainty evaluation of the entire process of measurement was profoundly studied. The analytical result of this work (14.53±0.15) nmol/g was in agreement with the certified value.

  14. Rb-Sr geochronology of the rocks of the Himalayas, Eastern Nepal, (2)

    International Nuclear Information System (INIS)

    Rb-Sr isotopic measurements are made on the Makalu granite, which is one of leucocratic granite occurring sporadically in the high range of the Himalayas. The granite is intruded between the Himalayan gneiss and the Tethyan sediments. In this study, Rb-Sr analyses have been made on both whole rock and small sliced rock. The Rb-Sr isotopic analytical results on whole rock of the Makalu granite define the age of 92.7 +- 9.4 m.y. The analytical results on small slabs suggest that Sr isotopic redistribution occurred after the intrusion of the granite. The initial 87Sr/86Sr ratio of the Makalu granite is 0.7433 +- 0.0019 and is remarkably high. Such high ratio indicates that the granite originated from the remelting or partial remelting of old crustal materials such as Himalayan gneiss. (author)

  15. Geochemistry, zircon U-Pb dating and Pb-Sr-Nd isotopic composition of the gneissic biotite granodiorite in Mainling County, Tibet%西藏米林县片麻状黑云花岗闪长岩地球化学特征、锆石U-Pb定年及Pb-Sr-Nd同位素组成

    Institute of Scientific and Technical Information of China (English)

    时超; 李荣社; 何世平; 王超; 辜平阳; 计文化; 查显锋; 张海迪

    2012-01-01

    The Himalayan orogenic belt, caused by the subduction and collision between Indian plate and Eurasian plate, is the youngest and largest currently active orogenic belt in the world. The LA-ICP-MS U-Pb zircon age of 515.5 ± 2.3 Ma from the gneissic biotite granodiorite that intruded into the Namche Barwa complex in eastern syntaxis of the Himalayan orogenic belt provides a geological record of Pan-African tectonic-mag-matic event in this area. The SiO2 content is 66.47% ~72.42%, the average of the A/CNK indexes is 1.03 (0.98 ~ 1.03), and all samples fall into the peraluminous region in the A/NK-A/CNK index diagram. The Rittmann index σ is between 1.53 and 3.08, belonging to the calc-alkaline series. Most of the samples fall into a high-K calc-alkaline series area in the SiQ ~ K2O diagram. The values of TiO2, MgO, FeOT , MnO and K2O show a good linear relationship with SiO2 content in the Harker diagrams. The chondrite-nomalized REE patterns indicate that the samples are enriched in LREE, (La/Yb)N values are 19.1~63.8, with slightly negative Eu anomalies (δEu = 0.62 ~0.79). Trace elements show the depletion of Ba, Nb, Ta, Sr and Z as well as the relative enrichment of Rb, Th and U. The negative e Nd(t) values(-8.67~-10.57) and Nd model ages (tdm= 1.84 ~ 3.42) of the gneissic biotite granodiorite of Tanya Township indicate that this rock had an old upper crust material source. Combined with the initial 87Sr/86Sr ratio features, the authors hold that the source rock of the gneissic biotite granodiorite of Tanya Township was granitic magma that partially melted in a high temperature environment. From the tectonic environment discrimination diagrams, it is inferred that metalumi-nous-weakly peraluminous gneissic biotite granodiorite of Tanya Township was formed in the post-collisional stage characterized by the conversion from a compressional environment to an extensional. Combined with the isotope age 513 Ma, the authors consider that the Pan-African collisional

  16. Pb isotopes during mingling and melting

    DEFF Research Database (Denmark)

    Waight, Tod Earle; Lesher, Charles E.

    2010-01-01

    Pb isotopic data are presented for hybrid rocks formed by mingling between mantle-derived tholeiitic magma of the Eocene Miki Fjord macrodike (East Greenland) and melt derived from the adjacent Precambrian basement. Bulk mixing and AFC processes between end-members readily identified in the field...... fail to model the Pb isotope systematics. Selective contamination during diffusional exchange, which can explain the complex Sr and Nd isotope compositions of the hybrid rocks (Blichert-Toft et al., 1992), cannot fully account for the variability of the Pb isotopic data using the identified crustal end......-members. The crustal anatectic end-member, although similar in Sr and Nd isotope composition, has a markedly different Pb isotopic composition than its source gneiss. The differences are consistent with preferential incorporation of radiogenic Pb from accessory phases such as metamict zircon or loosely-bound Pb from...

  17. High-precision measurement of variations in calcium isotope ratios in urine by multiple collector inductively coupled plasma mass spectrometry

    Science.gov (United States)

    Morgan, J.L.L.; Gordon, G.W.; Arrua, R.C.; Skulan, J.L.; Anbar, A.D.; Bullen, T.D.

    2011-01-01

    We describe a new chemical separation method to isolate Ca from other matrix elements in biological samples, developed with the long-term goal of making high-precision measurement of natural stable Ca isotope variations a clinically applicable tool to assess bone mineral balance. A new two-column procedure utilizing HBr achieves the purity required to accurately and precisely measure two Ca isotope ratios (44Ca/42Ca and 44Ca/43Ca) on a Neptune multiple collector inductively coupled plasma mass spectrometer (MC-ICPMS) in urine. Purification requirements for Sr, Ti, and K (Ca/Sr > 10000; Ca/Ti > 10000000; and Ca/K > 10) were determined by addition of these elements to Ca standards of known isotopic composition. Accuracy was determined by (1) comparing Ca isotope results for samples and standards to published data obtained using thermal ionization mass spectrometry (TIMS), (2) adding a Ca standard of known isotopic composition to a urine sample purified of Ca, and (3) analyzing mixtures of urine samples and standards in varying proportions. The accuracy and precision of δ44/42Ca measurements of purified samples containing 25 μg of Ca can be determined with typical errors less than ±0.2‰ (2σ).

  18. Isotopic compositions of strontium in river water of Guizhou karst areas, China

    Institute of Scientific and Technical Information of China (English)

    韩贵琳; 刘丛强

    2001-01-01

    We have carried out a study on the variation of strontium isotope composition of river waters, Wujiang and Yuangjiang River, in karst areas of Guizhou Province, China. The results obtained permit us to characterize the geochemistry of the river draining karst terrain and obtain a better understanding of main controls of catchment geology, chemical weathering of different rocks, and evaluate impact of human activities on the environment. The isotopic ratios of dissolved Sr in all rivers are between 87Sr/86Sr =0.7077 and 0.7110, totally lower than the weighted average of 87Sr/86Sr =0.7119 for the world large rivers. The Wujiang River waters have Sr concentrations from 1.0 to 6.1 μmol/L, while the Yuanjiang River waters have much lower Sr concentrations ranging from 0.28 to 1.3 μmol/L. Most of the river waters from the Wujiang river are characterized by low Ca/Sr and Mg/Sr, and 87Sr/86Sr ratios, in which a majority of river waters are of 87Sr/86Sr ratios lower than the average Sr isotope ratio (87Sr/86Sr

  19. Strontium isotope ratios - a possible tool to study the authenticity of Indian tea using MC-ICP-MS

    International Nuclear Information System (INIS)

    In the present study, an analytical procedure based on determination of the Sr isotope ratio 87Sr/86Sr in the Indian tea samples by MC-ICP-MS was developed and applied to 28 tea samples from four different Indian regions. The 87Sr/86Sr isotope ratio of the tea samples in different Indian regions is strongly dependent on the soil and growth environment condition. The analysis results of 28 Indian tea samples revealed that 87Sr/86Sr atom ratio follows the order Darjeeling > Kangra > Assam > Munnar

  20. Chromium isotopes in carbonates — A tracer for climate change and for reconstructing the redox state of ancient seawater

    DEFF Research Database (Denmark)

    Frei, Robert; Gaucher, Claudio; Døssing, Lasse Nørbye;

    2011-01-01

    climatic changes. We here present results of a new isotopic tracer system – stable chromium isotopes – applied to a late Ediacaran marine carbonate sequence exposed in the Calera de Recalde syncline, Arroyo del Soldado Group, Uruguay. The aim was to compare Cr isotope signatures directly to d13C, 87Sr/86Sr...

  1. Areal distribution of 60Co, 137Cs, and 90Sr in streambed gravels of White Oak Creek Watershed, Oak Ridge, Tennessee

    International Nuclear Information System (INIS)

    The concentrations of 90Sr, 60Co, and 137Cs in streambed gravels from contaminated drainages in White Oak Creek Watershed were determined. Methods to determine the relative contributions of various sources to the total discharge from the watershed were developed. Principal sources of 90Sr were: ORNL plant effluents (50%), leaching from solid waste disposal area (SWDA) 4 (30%), and leaching from SWDA 5 (10%). Minor sources included SWDA 3, the Molten Salt Reactor Facility, and intermediate-level liquid waste pit 1 with each representing 4% or less of the total basin discharge. The cooling water effluent from the High-Flux Isotope Reactor was the dominant source of 60Co contamination in the watershed. ORNL plant effluents accounted for almost all the 137Cs discharge from White Oak Creek basin. Downstream radionuclide concentrations were constant until significant dilution by other tributaries occurred. Any future activities giving rise to additional contamination can now be identified. Distribution coefficients between streambed gravels and streamwater for 85Sr, 60Co, and 137Cs were 50, 560, and 8460 ml/g, respectively. An abridged radiochemical fractionation developed for 90Sr was found to be as accurate and precise for these samples as the standard 90Sr method above levels of 2 dpm/g

  2. Bose-Einstein condensation of 84Sr.

    Science.gov (United States)

    Martinez de Escobar, Y N; Mickelson, P G; Yan, M; DeSalvo, B J; Nagel, S B; Killian, T C

    2009-11-13

    We report Bose-Einstein condensation of (84)Sr in an optical dipole trap. Efficient laser cooling on the narrow intercombination line and an ideal s-wave scattering length allow the creation of large condensates (N(0) approximately 3 x 10(5)) even though the natural abundance of this isotope is only 0.6%. Condensation is heralded by the emergence of a low-velocity component in time-of-flight images. PMID:20365965

  3. Bose-Einstein Condensation of 84-Sr

    OpenAIRE

    de Escobar, Y. N. Martinez; Mickelson, P. G.; Yan, M; DeSalvo, B. J.; Nagel, S. B.; Killian, T. C.

    2009-01-01

    We report Bose-Einstein condensation of 84-Sr in an optical dipole trap. Efficient laser cooling on the narrow intercombination line and an ideal s-wave scattering length allow creation of large condensates (N0 ~ 3x10^5) even though the natural abundance of this isotope is only 0.6%. Condensation is heralded by the emergence of a low-velocity component in time-of-flight images.

  4. 川东北宋家洞石笋氧碳同位素及锶含量突变分析%Abrupt Change Analyses of Oxygen, Carbon Isotope Values and Sr Contents in a Stalagmite Retrieved from Songjia Cave, NE Sichuan

    Institute of Scientific and Technical Information of China (English)

    曹益瑰; 李娇; 汤静

    2012-01-01

    通过对宋家洞石笋SJ3的氧碳同位素及锶含量进行Mann—Kendalltest突变分析,得出以下结论:(1)氧同位素值记录了末次冰盛期向HeinrichEvent1时期的转变;(2)碳同位素值和锶含量记录了由H1冷期向Boiling—Allemd暖期的转变;(3)碳同位素值和锶含量指示了在19.8~15.3ka时当地的东亚夏季风和冬季风呈正相关关系,在15.3~14.8ka呈负相关关系,表明石笋SJ3记录了古气候环境的冷干、暖湿变化,且不同气候指标对环境变化的敏感度不同。%We analyze the abrupt changes of oxygen, carbon isotope values and Sr contents in stalagmite S J3 retrieved from Songjia Cave, Central China. Some conclusions are given below : ( 1 ) Oxygen isotope values record the transition from Last Glacial Maximum to Heinrich Event One period;(2) Carbon isotope values record the transition from H1 cold period to BoilingAllerod warm period ; (3) The correlation between Carbon isotope values and Sr contents indicate that the local East Asian summer monsoon were in - phase with the winter monsoon during 19.8 - 15.3ka while out of phase during 15.3 - 14.8ka. It' s obvious that stalagmite SJ3 records the palaeoclimate changes between colddry and warmwet conditions while different climate proxies were dissimilar in sensitivities with regard to climate changes.

  5. Calibration of amino acid racemization (AAR) kinetics in United States mid-Atlantic Coastal Plain Quaternary mollusks using 87Sr/ 86Sr analyses: Evaluation of kinetic models and estimation of regional Late Pleistocene temperature history

    Science.gov (United States)

    Wehmiller, J. F.; Harris, W.B.; Boutin, B.S.; Farrell, K.M.

    2012-01-01

    The use of amino acid racemization (AAR) for estimating ages of Quaternary fossils usually requires a combination of kinetic and effective temperature modeling or independent age calibration of analyzed samples. Because of limited availability of calibration samples, age estimates are often based on model extrapolations from single calibration points over wide ranges of D/L values. Here we present paired AAR and 87Sr/ 86Sr results for Pleistocene mollusks from the North Carolina Coastal Plain, USA. 87Sr/ 86Sr age estimates, derived from the lookup table of McArthur et al. [McArthur, J.M., Howarth, R.J., Bailey, T.R., 2001. Strontium isotopic stratigraphy: LOWESS version 3: best fit to the marine Sr-isotopic curve for 0-509 Ma and accompanying Look-up table for deriving numerical age. Journal of Geology 109, 155-169], provide independent age calibration over the full range of amino acid D/L values, thereby allowing comparisons of alternative kinetic models for seven amino acids. The often-used parabolic kinetic model is found to be insufficient to explain the pattern of racemization, although the kinetic pathways for valine racemization and isoleucine epimerization can be closely approximated with this function. Logarithmic and power law regressions more accurately represent the racemization pathways for all amino acids. The reliability of a non-linear model for leucine racemization, developed and refined over the past 20 years, is confirmed by the 87Sr/ 86Sr age results. This age model indicates that the subsurface record (up to 80m thick) of the North Carolina Coastal Plain spans the entire Quaternary, back to ???2.5Ma. The calibrated kinetics derived from this age model yield an estimate of the effective temperature for the study region of 11??2??C., from which we estimate full glacial (Last Glacial Maximum - LGM) temperatures for the region on the order of 7-10??C cooler than present. These temperatures compare favorably with independent paleoclimate information

  6. The 87Sr/86Sr aquatic isoscape of the Danube catchment from the source to the mouth as tool for studying fish migrations

    Science.gov (United States)

    Zitek, Andreas; Tchaikovsky, Anastassiya; Irrgeher, Johanna; Waidbacher, Herwig; Prohaska, Thomas

    2014-05-01

    Isoscapes - spatially distributed isotope patterns across landscapes - are increasingly used as important basis for ecological studies. The natural variation of the isotopic abundances in a studied area bears the potential to be used as natural tracer for studying e.g. migrations of animals or prey-predator relations. The 87Sr/86Sr ratio is one important tracer, since it is known to provide a direct relation of biological samples to geologically distinct regions, as Sr isotopes are incorporated into living tissues as a proxy for calcium and taken up from the environment without any significant fractionation. Although until now the focus has been mainly set on terrestrial systems, maps for aquatic systems are increasingly being established. Here we present the first 87Sr/86Sr aquatic isoscape of the Danube catchment, the second largest river catchment in Europe, from near its source starting at river km 2581 in Germany down to its mouth to river km 107 in Romania. The total length of the river Danube is 2780 km draining a catchment area 801 463 km2 (10 % of the European continent). The major purpose of this study was to assess the potential of the 87Sr/86Sr isotope ratio to be used as tool for studying fish migrations at different scales in the entire Danube catchment. Within the Joint Danube Research 3 (JDS 3), the biggest scientific multi-disciplinary river expedition of the World in 2013 aiming at the assessment of the ecological status and degree of human alterations along the river Danube, water samples were taken at 68 pre-defined sites along the course of the river Danube including the major tributaries as a basis to create the so called 'Isoscape of the Danube catchment'. The determination of 87Sr/86Sr isotope ratio in river water was performed by multicollector-sector field-inductively coupled plasma-mass spectrometry (MC-SF-ICP-MS). The JDS 3 data were combined with existing data from prior studies conducted within the Austrian part of the Danube catchment

  7. The evolution of the 87Sr/86Sr in the Dead Sea brine: from the Sedom lagoon to Sahara dusts

    Science.gov (United States)

    Stein, Mordechai

    2016-04-01

    The history of water-bodies in the Dead Sea brines commenced with the intrusion of the Sedom lagoon, possibly in the late Neogene and continued with the development of hypersaline and freshwater lakes (e.g. the modern Dead Sea and Sea of Galilee). 87Sr/86Sr ratios in these water-bodies decreased over the past ~ 5-6 Ma from 0.7087-0.7084 in salts deposited in the Sedom lagoon to ~ 0.7080 in modern Dead Sea brine. The 87Sr/86Sr ratios in the salts deposited from Sedom lagoon are significantly lower than those of the contemporaneous late Miocene seawater (~0.709). This difference was attributed to modification of the 87Sr/86Sr ratio in the Sedom lagoon solution by influx of Ca-chloride brines. The brines, in turn were formed by dolomitization of marine limestones of the DSR Cretaceous wall rocks (87Sr/86Sr ~ 0.7075) by the ingressing evaporated seawaters (Stein et al., 2000). After the disconnection of the Sedom lagoon from the open sea freshwater filled the lakes that occupied the Dead Sea basin. The freshwater influx modified the strontium isotope and chemical composition of the brine and provided bicarbonate and sulfate to the lake that led the precipitation of primary aragonite and gypsum. Freshwater that currently enter the lake are characterize by 87Sr/86Sr ~ 0.7081, significantly higher than the Cretaceous carbonates. Settled dust that deposits on the Judea Mountains is composed of calcite and quartz grains and is characterized by 87Sr/86Sr ratios ~ 0.7084. It appears that significant amounts of the strontium that entered the lakes with the freshwater originated from dissolution of the dust calcites. Large amounts of dust were transported from the Sahara desert to the Dead Sea watershed during glacial periods when the Sahara was dry and sea-level was low. The source of the detrital calcites however, is not known. They could be derived from dry paleo-lakes in the Sahara that were previously filled by waters that retained the required strontium isotope

  8. Geochemical and mantle-like isotopic (Nd, Sr) composition of the Baklan Granite from the Muratdağı Region (Banaz, Uşak), western Turkey: Implications for input of juvenile magmas in the source domains of western Anatolia Eocene Miocene granites

    Science.gov (United States)

    Aydoğan, M. Selman; Çoban, Hakan; Bozcu, Mustafa; Akıncı, Ömer

    2008-07-01

    The (late syn)- post-collisional magmatic activities of western and northwestern Anatolia are characterized by intrusion of a great number of granitoids. Amongst them, Baklan Granite, located in the southern part of the Muratdağı Region from the Menderes Massif (Banaz, Uşak), has peculiar chemical and isotopic characteristics. The Baklan rocks are made up by K-feldspar, plagioclase, quartz, biotite and hornblende, with accessory apatite, titanite and magnetite, and include mafic microgranular enclaves (MME). Chemically, the Baklan intrusion is of sub-alkaline character, belongs to the high-K, calc-alkaline series and displays features of I-type affinity. It is typically metaluminous to mildly peraluminous, and classified predominantly as granodiorite in composition. The spider and REE patterns show that the rocks are fractionated and have small negative Eu anomalies (Eu/Eu ∗ = 0.62-0.86), with the depletion of Nb, Ti, P and, to a lesser extent, Ba and Sr. The pluton was dated by the K-Ar method on the whole-rock, yielded ages between 17.8 ± 0.7 and 19.4 ± 0.9 Ma (Early Miocene). The intrusion possesses primitive low initial 87Sr/ 86Sr ratios (0.70331-0.70452) and negative ɛNd(t) values (-5.0 to -5.6). The chemical contrast between evolved Baklan rocks (SiO 2, 62-71 wt.%; Cr, 7-27 ppm; Ni, 5-11 ppm; Mg#, 45-51) and more primitive clinopyroxene-bearing monzonitic enclaves (SiO 2, 54-59 wt.%; Cr, 20-310 ppm; Ni, 10-70 ppm; Mg#, 50-61) signifies that there is no co-genetic link between host granite and enclaves. The chemical and isotopic characteristics of the Baklan intrusion argue for an important role of a juvenile component, such as underplated mantle-derived basalt, in the generation of the granitoids. Crustal contamination has not contributed significantly to their origin. However, with respect to those of the Baklan intrusion, the generation of the (late syn)- post-collisional intrusions with higher Nd(t) values from the western Anatolia require a much

  9. 西藏冈底斯厅宫铜矿侵入岩成因:LA-ICP-MS 锆石U-Pb 年龄、地球化学及 Sr-Nd-Pb 同位素证据%Petrogenesis of Intrusions in Tinggong Copper Deposit,Gangdese, Xizang(Tibet):Evidence from LA-ICP-MS Zircon U-Pb Dating, Petrogeochemical,and Sr-Nd-Pb Isotopic Composition

    Institute of Scientific and Technical Information of China (English)

    黄勇; 丁俊; 李光明; 董随亮; 黄瀚霄; 崔晓亮; 戴婕; 闫国强

    2015-01-01

    studies of above major granites are benefited for future exploration.LA-ICP-MS zircon U-Pb dating,major and trace elements,Rb-Sr,Sm-Nd,Pb isotope composition were test by this study.The results show that the age of above granites are 50.32 Ma,48.34 Ma,and 49.41 Ma,respectively,which are apparently older than that of mineralization.Above stocks belong to high-K calc-alkaline,weakly peraluminous,I-type granites.The REE patterns indicate a LREE rich,with weak /no HREE fractionation V-type model and strong depleted δEu,which are reverse with SiO2 content.All granites are rich in Th,U,K,Cs,and Rb,depleted in Ba,Nb,Sr,Ti.Whole rock Pb isotopic compositions show that calculated n(206 Pb)/n(204 Pb)n(207 Pb)/n(204 Pb),n(208 Pb)/n(204 Pb) are 18.414 ~18.5137,15.616 ~15.7039,38.6394 ~39.0029,respectively,indicating a high radio-Pb isotope composition.Calculated n(87 Sr)/n(86 Sr)and n(143 Nd)/n(144 Nd)restrict in narrow range:0.70320 ~0.70477, 0.51260 ~0.51265,respectively,with calculated positive εNd (t)(0.51 ~1.44).The above results indicate that spread magna are not related to the mineralization and derived from new lower crust/depleted mantle during the roll-back and break-off of northward subducted ocean crust,undergoing AFC process during emplace.

  10. Lithogeochemistry and Sr-Nd-Pb Isotopic Characteristics of Mujicun Porphyry Cu-Mo Deposit in Taihang Mountains and Their Significances%太行山木吉村斑岩铜(钼)矿床岩石地球化学、S r-Nd-Pb同位素特征及其地质意义

    Institute of Scientific and Technical Information of China (English)

    曲凯; 董国臣; 李胜荣; 申俊峰; 王艳娟; 王霞; 罗薇

    2014-01-01

    Mujicun porphyry copper-molybdenum deposit, located in the northern section of Taihang Mountains,is an important ore deposit in the Taihang tectonic-magmatic-metallogenic belt.This article is based on the particular field works and systematic analysis of petrology,geochemical data and Sr-Nd-Pb isotopes.The result shows the ore-bearing diorite-porphyry of Mujicun belonging to the high-K calc-alkaline I-type intrusive rock.Geochemical analysis shows that the diorite-porphyry is rich in SiO2,Al2O3 and Sr,a high ratio of Sr/Y, (La/Yb)N ,low in Yb and Y.All the ore-bearing porphyries in the study area have similar distribution of rare earths and trace elements,with right-oblique curve,and unclear postive Eu anomalies.It is characterized by enriched large-ion lithophile elements of Ba,K,U,Sr and depleted high field strength elements such as Nb, Ta,P and Ti with adakite affinity in geochemical characteristic.The diorite porphyry has ISr ratios of 0.705 386 to 0.706 838,εNd(t)values of -16.7 to -14.9.The averages of 208Pb/204Pb,207Pb/204Pb and 206Pb/204Pb ratios are 36.614,15.226 and 16.545,respectively,similar to those lead isotope ratios in ore of Mujicun de-posit.Sr-Nd-Pb isotopes show that the formations of the magma were probably related to origin of partial melting of lower crust with mantle materials contribution.Combining with the geological background of the study area, the authors considered that the Mujicun ore-bearing diorite porphyry possibly resulted from partial melting in lower crust with the mantle mass exchange.%木吉村斑岩铜(钼)矿床位于太行山北段涞源杂岩体的腰部,是太行山构造-岩浆-成矿带的一个重要矿床。在野外调研的基础上,对木吉村斑岩铜(钼)矿床含矿岩体进行了系统的岩石学、地球化学和Sr-Nd-Pb同位素研究。结果表明:木吉村矿床的含矿岩体闪长玢岩为高钾钙碱性I型侵入岩,具有较高的SiO2、Al2 O3、Sr含量和Sr

  11. Sr and Nd isotopic signature of the high-K calc-alkaline magmatism of the central Ribeira belt: the Sao Pedro Granite in Lumiar, RJ; Assinatura isotopica de Sr e Nd do magmatismo calcio-alcalino de alto-K na Faixa Ribeira central: o exemplo do Granito Sao Pedro em Lumiar, RJ

    Energy Technology Data Exchange (ETDEWEB)

    Mendes, Julio Cezar; Medeiros, Silvia Regina de; Chaves, Eduardo Amorim, E-mail: julio@geologia.ufrj.br, E-mail: silvia@geologia.ufrj.br, E-mail: edupc2@yahoo.com.br [Departamento de Geologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro (RJ) (Brazil)

    2011-09-15

    In the central-northern Ribeira belt there are many granitic to granodioritic bodies showing varied shape and size, characterizing a late- to post-collisional Ca-alkaline, cordilleran I-type province. The Sao Pedro Granite occurs in the mountain region of Rio de Janeiro State as small post-collisional bodies. It presents isotropic fabric, equigranular to seriate inequigranular texture, as well as local concentration of allanite, which gives discrete composition and texture variation to the rock. The granite has a high-K calcalkaline to alkali-calcic character and weakly peraluminous nature. Despite its short geochemical variation, high Ba, Zr and Th contents besides low concentrations of MgO and CaO are noticeable. High REE contents are associated with fractionated REE patterns showing strong negative Eu anomalies. A crustal origin for the granite can be assumed by its very negative and positive .Nd and .Sr values, respectively, as well as by 87Sr/86Sr initial ratios ranging from 0,718 to 0,740. TDM ages point to paleoproterozoic source, which agrees with geological time of intensive crust generation. (author)

  12. Petrogenesis and tectonic implications of the high-K Alamas calc-alkaline granitoids at the northwestern margin of the Tibetan Plateau: Geochemical and Sr-Nd-Hf-O isotope constraints

    Science.gov (United States)

    Zhang, Qichao; Liu, Yan; Huang, He; Wu, Zhenhan; Zhou, Qing

    2016-09-01

    The Alamas granitoid pluton in the eastern part of the Western Kunlun Orogen, the northwestern margin of the Tibetan Plateau, is composed of quartz diorite. Zircon separates from the pluton has SIMS U-Pb age of ∼446 Ma. Rocks from the pluton have a narrow range of SiO2 (56.84-62.57 wt%), MgO (1.76-2.94 wt%), and total alkalis (Na2O + K2O = 5.14-9.59 wt%), and are metaluminous and high-K calc-alkaline to shoshonitic in composition. They are enriched in light rare earth elements (LREEs), with (La/Yb)N = 14-25, and show weakly negative Eu anomalies. These rocks are relatively enriched in Sr (472-676 ppm) and Ba (435-2388 ppm), and depleted in Nb, Ta, Th, and Ti. Their εNd(t) values range from -6.4 to -8.4, and (87Sr/86Sr)i = 0.7184-0.7200. Zircons from the pluton show εHf(t) values of -1.4 to -8.8, and δ18O = 6.4-9.0‰. Geochemical data indicate that the granitoids were likely derived from the reworking of an ancient, deep crustal source, influenced by a minor mantle-derived component. Magmatic differentiation was dominated by the fractional crystallization of hornblende, biotite, and accessory minerals such as apatite, allanite, and Fe-Ti oxides. In summary, the Late Ordovician Alamas pluton is an I-type granitoid that was emplaced in a post-collisional environment, suggesting that this tectonic stage had already initiated prior to ∼445 Ma.

  13. Tank waste isotope contributions

    International Nuclear Information System (INIS)

    This document presents the results of a calculation to determine the relative contribution of selected isotopes to the inhalation and ingestion doses for a postulated release of Hanford tank waste. The fraction of the dose due to 90Sr, 90Y, 137Cs and the alpha emitters for single shell solids and liquids, double shell solids and liquids, aging waste solids and liquids and all solids and liquids. An effective dose conversion factor was also calculated for the alpha emitters for each composite of the tank waste

  14. The Strontium Isotope Record of Zavkhan Terrane Carbonates: Strontium Isotope Stability Through the Ediacaran-Cambrian Transition

    OpenAIRE

    Petach, Tanya N.

    2015-01-01

    First order trends in the strontium isotopic (87Sr/86Sr) composition of seawater are controlled by radiogenic inputs from the continent and non-radiogenic inputs from exchange at mid-ocean ridges. Carbonates precipitated in seawater preserve trace amounts of strontium that record this isotope ratio and therefore record the relative importance of mid-ocean ridge and weathering chemical inputs to sea water composition. It has been proposed that environmental changes during the Ediacaran-Cambria...

  15. Isotopic signatures of lamproite dikes on the eastern Baltic shield

    International Nuclear Information System (INIS)

    The age values, coinciding by Rb-Sr and Sm-Nd, are obtained for lamproits in the eastern party of the Baltic Shield (the Kostamuksha Region): 1230±5 Ma and 1234±80 Ma correspondingly. The magnetic source of lamproites is depletary relative to the Sr isotope composition and enriched relative to the Nd composition

  16. Strontium isotope evidence on the history of oilfield brines, Mediterranean Coastal Plain, Israel

    Energy Technology Data Exchange (ETDEWEB)

    Starinsky, A.; Bielski, M.; Lazar, B. (Hebrew Univ., Jerusalem (Israel). Dept. of Geology); Steinitz, G.; Raab, M. (Geological Survey of Israel, Jerusalem)

    1983-04-01

    The isotopic composition of Sr in oil field brines from the Mediterranean Coastal Plain was determined in 18 drillholes. The brines are characterized by salinities ranging from 35 to 93 g/l (TDS), Sr from 28 to 350 mg/l, Sr/Ca molar ratios from 0.011 to 0.053 and /sup 87/Sr//sup 86/Sr ratios from 0.7075 to 0.7090. E and A = 0.7081 +- 0.0004 (2sigma). The brines are classified into two groups: (a) Mavqi'im group - brines with relatively high /sup 87/Sr//sup 86/Sr ratios, sampled from clastics, dolomites and anhydrites of Upper Miocene age. (b) Heletz group - brines with relatively low /sup 87/Sr//sup 86/Sr ratios, sampled from sandstones and dolomites of Lower Cretaceous age. Equations were derived to show the relations between /sup 87/Sr//sup 86/Sr ratio of the brines and the processes through which they evolved. It is suggested that both groups of brines originated from Mediterranean evaporated seawater during the Messinian desiccation. The strontium isotope composition of the seawater is reflected in that of both groups of brines, the Mavqi'im group containing the original /sup 87/Sr//sup 86/Sr ratio. The Heletz group evolved later on, through exchange reactions of those primary brines with a carbonate sequence of Cretaceous age and consequently new /sup 87/Sr//sup 86/Sr ratios could have been developed.

  17. Pb-Pb age and Rb-Sr and Sm-Nd isotope signature of paleoproterozoic syenitic plutonism in the south of Salvador-Curaca mobile belt: Sao Felix Syenitic Massif, Bahia-Brazil

    International Nuclear Information System (INIS)

    The Sao Felix Syenitic Massif (MSSF) has a tabular shape with about 32 km2 that represents the south expression of the aligned syenitic plutonism, which occur in the middle part of Salvador-Curaca mobile belt (CMSC). Single zircon dating by stepwise Pb evaporation methodology yields an age of 2098 ± 1 Ma to SFSM. This data correlate the emplacement of the SFSM with the late stages of SCMB stabilization. This massif is isotopically characterized by negative epsilon neodymium values (-1.45 to -2.89) and low initial strontium ratio (0.701 to 0.704). SFSM isotopic signature is similar to the ones displayed by the others syenites from the belt and reflects an enriched source which should be related to a metasomatic enriched mantle. (author)

  18. 液相色谱-同位素稀释质谱法准确测定人血清中葡萄糖含量%Accurate Determination of Serum Glucose by Liquid Chromatography-Isotope Dilution Mass Spectrometry

    Institute of Scientific and Technical Information of China (English)

    申玉星; 全灿; 马康

    2011-01-01

    以D-[13C6]葡萄糖标记物作为内标,用高效液相色谱-串联质谱法测定血清中的葡萄糖含量.向室温平衡后的血清样品中加入葡萄糖标记物,用乙醇沉淀蛋白,低温离心去除蛋白,上清液过0.22 μm有机滤膜.采用LC/MS电喷雾离子源(ESI),正离子模式,选择离子监测模式进行检测.方法的线性相关系数R2 =0.999 5,加标回收率为100.1%~102.8%,检出限为8μg/kg,相对标准偏差0.49%.该方法的样品前处理简单,测定准确高、精密度好,可用于血清中葡萄糖含量的高准确度定值.%A high performance liquid chromatography tandem mass spectrometric method was established for the determination of glucose concentration in serum with the aid of D-[13C6] glucose internal standard. D-[13 C6 ] glucose was added to the serum sample in balance at room temperature. Then the protein was precipitated and extracted in anhydrous ethanol with centrifugation at low temperature. The supernatant was filtered through a 0. 22 μm syringe filter into HPLC vials. Identification was achieved by electro-spray ionization (ESI) in positive mode using SIM mode. The calibration curve of glucose showed good linearity with correlation coefficient of R2=0. 999 5, recoveries of spiked samples were in the range 100. 1% to 102. 8%, the detection limit of the method was 8 μg/kg (S/N = 3) , and the relative standard derivations were 0. 49%. The established method is simple, accurate and precise, is appropriate for the determination of serum glucose with great accuracy.

  19. Hydrogeochemistry and strontium isotopes of spring and mineral waters from Monte Vulture volcano, Italy

    International Nuclear Information System (INIS)

    This paper describes the results of a study that was conducted to determine the relationship between hydrogeochemical composition and 87Sr/86Sr isotope ratios of the Mt. Vulture spring waters. Forty samples of spring waters were collected from local outcrops of Quaternary volcanites. Physico-chemical parameters were measured in the field and analyses completed for major and minor elements and 87Sr/86Sr isotopic ratios. A range of water types was distinguished varying from alkaline-earth bicarbonate waters, reflecting less intense water-rock interaction processes to alkali bicarbonate waters, probably representing interaction with volcanic rocks of Mt. Vulture and marine evaporites. The average 87Sr/86Sr isotope ratios suggest at least 3 different sources. However, some samples have average Sr isotope ratios (0.70704-0.70778) well above those of the volcanites. These ratios imply interaction with other rocks having higher 87Sr/86Sr ratios, probably Triassic evaporites, which is substantiated by their higher content of Na, SO4 and Cl. The Sr isotope ratios for some samples (e.g. Toka and Traficante) are intermediate between the value for the Vulture volcanites and that for the local Mesozoic rocks. The salt content of these samples also lies between the value for waters interacting solely with the volcanites and the value measured in the more saline samples. These waters are thus assumed to result from the mixing of waters circulating in volcanic rocks with waters presumably interacting with the sedimentary bedrock (marine evaporites)

  20. Use of 87Sr/86Sr and δ11B to Identify Slag-Affected Sediment in Southern Lake Michigan

    Science.gov (United States)

    Bayless, Randall; Bullen, Thomas D.; Fitzpatrick, John A.

    2004-01-01

    Slag is a ubiquitous byproduct of the iron-smelting industry and influences geochemistry and water quality in adjacent geologic units, ground and surface water. Despite extensive slag deposition along the Indiana shoreline of Lake Michigan, definitive evidence that slag has affected lakebed sediments has not been established. Concerns for the protection of water and ecosystem resources in the Great Lakes motivated this study to determine if strontium and boron isotopes could be used to identify and delineate slag-affected bed sediment in Lake Michigan. Sixty-five samples of bed sediment were acquired from the southern lobe of Lake Michigan and analyzed for 87Sr/86Sr and ??11B. Samples immediately offshore from Indiana steel mills and slag-disposal sites contained higher median 87Sr/86Sr values (0.70881) than shoreline sediments collected elsewhere in the basin (0.70847) and uniquely decreased with increasing distance from the shoreline. The highest ??11B values occurred in sediments from the Indiana shoreline (+12.9 to 16.4???) but were also elevated in sediments collected offshore from three Lake Michigan cities (+11.7 to 12.7???). Contoured isotope data indicated that 82-154 km2 of bed sediment along the Indiana shoreline had elevated 87Sr/86Sr and ??11B values relative to shoreline sediments elsewhere in southern Lake Michigan.

  1. High-purity enrichment of 84Sr

    International Nuclear Information System (INIS)

    High-purity 84Sr (i.e., >99 at %) is an important tool in many areas of basic and applied research, in particular for spikes used in isotopic dilution/mass spectrometer investigations in geochemistry, cosmochemistry, and paleoclimate-age studies. In nature, the 84Sr abundance is only 0.56%; however, it can be enriched to the specified requirements by using a high-resolution separator, such as the 180 deg. -sector separator, or by completing two passes through a high-production, lower-resolution machine, such as the calutron. The latter option was used for this enrichment to produce ∼1 g of strontium with a final 84Sr concentration of 99.64%. Three innage runs were made, vaporizing a total of ∼17 g of metal feed that had been pre-enriched in the calutron to ∼70% 84Sr. A partial recovery, followed by recycle of the unresolved feed, was made after the second innage run. A process efficiency of 8.44% was achieved, and 4.33 g of the unresolved feed material was recovered. A modified ion-source unit using materials compatible with strontium and the use of krypton as mass markers to aid in operations are described. Standard contamination analyses were performed to evaluate the enrichment and to compare measured results with predicted product purity

  2. Isotopic geology

    International Nuclear Information System (INIS)

    Born from the application to geology of nuclear physics techniques, the isotopic geology has revolutionized the Earth's sciences. Beyond the dating of rocks, the tracer techniques have permitted to reconstruct the Earth's dynamics, to measure the temperatures of the past (giving birth to paleoclimatology) and to understand the history of chemical elements thanks to the analysis of meteorites. Today, all domains of Earth sciences appeal more or less to the methods of isotopic geology. In this book, the author explains the principles, methods and recent advances of this science: 1 - isotopes and radioactivity; 2 - principles of isotope dating; 3 - radio-chronological methods; 4 - cosmogenic isotope chronologies; 5 - uncertainties and radio-chronological results; 6 - geochemistry of radiogenic isotopes; 7 - geochemistry of stable isotopes; 8 - isotopic geology and dynamical analysis of reservoirs. (J.S.)

  3. Isotopic clusters

    International Nuclear Information System (INIS)

    Spectra of isotopically mixed clusters (dimers of SF6) are calculated as well as transition frequencies. The result leads to speculations about the suitability of the laser-cluster fragmentation process for isotope separation. (Auth.)

  4. Anglo-Saxon animal husbandry techniques revealed though isotope and chemical variations in cattle teeth

    Energy Technology Data Exchange (ETDEWEB)

    Evans, J.A. [NERC Isotope Geosciences Laboratory, BGS, Keyworth, Nottingham NG12 5GG (United Kingdom)], E-mail: je@nigl.nerc.ac.uk; Tatham, S. [School of Archaeology and Ancient History, University of Leicester, Leicester LE1 7RH (United Kingdom); Chenery, S.R. [British Geological Survey, Keyworth, Nottingham NG12 5GG (United Kingdom); Chenery, C.A. [NERC Isotope Geosciences Laboratory, BGS, Keyworth, Nottingham NG12 5GG (United Kingdom)

    2007-09-15

    The Sr concentration and isotope composition of tooth enamel from domesticated animals from two neighbouring Anglo-Saxon settlements, at Empingham (6-7th century) and Ketton (10-12th century) in Rutland, central England, are compared both with each other, and with associated human populations. Data from the Empingham II site form discrete fields in Sr concentration and isotope composition space for cattle, pig and sheep with a partial overlap of the human and pig fields. By contrast there is significant overlap in all the animal and human data fields from the Ketton site. The differences in data distribution between the two sites are attributed to animal husbandry techniques, as the surface geology of the two areas is very similar, implying geological factors are an unlikely cause of the difference. It is suggested that the grazing and feeding patterns of animals at the Empingham II site were controlled and restricted, whereas at the Ketton site the animals grazed and foraged freely over a common area. Strontium isotope variation within cattle molars from the two settlements show marked differences that reflect the nature of their feeding and rearing. The enamel from a cattle molar from the Empingham II site has a well-defined, systematic variation of Sr isotope composition with Sr concentration, whereas no such patterns exist in a comparable cattle molar from Ketton. Chemical and O isotope variations in the cattle tooth from Empingham II show sympathetic variation of Sr and Ba concentrations with Sr isotope composition from cusp to cervix. The cusp has higher Sr and Ba concentrations log (Sr/Ca) ratio of -3.1 and {sup 87}Sr/{sup 86}Sr ratio of 0.71151 where as the cervical region of the enamel has log (Sr/Ca) = -3.3 and {sup 87}Sr/{sup 86}Sr = 0.71061.

  5. Radiogenic age and isotopic studies

    International Nuclear Information System (INIS)

    This is one of an annual collection of reports presenting data from the Geochronology Section of the Continental Geoscience Division of the Geological Survey of Canada (GSC). The main purpose of this collection is to make geochronological and other radiogenic isotope data produced by the section available promptly to the geological community. Reports make full presentation of the data, relate these to field settings and make comparatively short interpretations. Other geochronological and isotope data produced in the laboratory but published in outside journals or separate GSC publications are summarized at the end of this report. Reports in this issue cover methods for Rb-Sr and Sm-Nd isotopic analyses; 40Ar-39Ar ages for the New Quebec Crater and for basaltic rocks; U-Pb ages for a differentiated mafic sill in the Ogilvie Mountains, plutonic rocks in the Contwoyto-Nose Lakes are, zircons from the Anton Complex, the Clinton-Colden gabbro-anorthosite intrusion, the Himag plutonic suite, the Campbell granite, the Central Gneiss Belt, Silurian granites, a metarhyolite, plagiogranite and gabbro, and the Wage shear zone; Rb-Sr ages for granitic rocks; K-Ar and Rb-Sr geochronology of granites; a compilation of K-Ar ages; ages of archean and proterozoic mylonites and pre-Misi granitoid domes; and reconnaissance geochronology of Baffin Island

  6. Mesures conjointes des rapports Sr/Ca et δ 18O effectuées sur Acropora nobilis et Pontes lutea: le paléothermomètre Sr/Ca est-il toujours fiable?

    Science.gov (United States)

    Boiseau, Muriel; Cornu, Hélène; Turpin, Laurent; Juillet-Leclerc, Anne

    1997-11-01

    We measured the Sr/Ca and 18O/ 16O ratios in Acropora nobilis and Porites lutea, from the Mayotte lagoon. As the variations of δ 18O seawater are negligible, coral δ 18O aragonite reflects only seasonal temperature variations. While there is a good agreement between the Sr/Ca ratio and δ 18O for Acropora nobilis, it is not the case for Porites lutea. Coral biological and environmental parameters cannot explain the discrepancies between Sr/Ca ratios and isotopic measurements. However, transport mechanisms of Sr 2+ and Ca 2+ and the presence of two mineralogical structures of strontium may affect the Sr/Ca ratio.