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Sample records for strontium isotope geochemistry

  1. Strontium isotopic geochemistry of intrusive rocks, Puerto Rico, Greater Antilles

    International Nuclear Information System (INIS)

    Jones, L.M.; Kesler, S.E.

    1980-01-01

    The strontium isotope geochemistry is given for three Puerto Rican intrusive rocks: the granodioritic Morovis and San Lorenzo plutons and the Rio Blanco stock of quartz dioritic composition. The average calculated initial 87 Sr/ 86 Sr ratios are 0.70370, 0.70355 and 0.70408, respectively. In addition, the San Lorenzo data establish a whole-rock isochron of 71 +- 2 m.y., which agrees with the previously reported K-Ar age of 73 m.y. Similarity of most of the intrusive rocks in the Greater Antilles with respect to their strontium isotopic geochemistry regardless of their major element composition indicates that intrusive magmas with a wide range of composition can be derived from a single source material. The most likely source material, in view of the available isotopic data, is the mantle wedge overlying the subduction zone. (orig.)

  2. Strontium isotope geochemistry of soil and playa deposits near Yucca Mountain, Nevada

    International Nuclear Information System (INIS)

    Marshall, B.D.; Mahan, S.A.

    1994-01-01

    The isotopic composition of strontium contained in the carbonate fractions of soils provides an excellent tracer which can be used to test models for their origin. This paper reports data on surface coatings and cements, eolian sediments, playas and alluvial fan soils which help to constrain a model for formation of the extensive calcretes and fault infillings in the Yucca Mountain region. The playas contain carbonate with a wide range of strontium compositions; further work will be required to fully understand their possible contributions to the pedogenic carbonate system. Soils from an alluvial fan to the west of Yucca Mountain show that only small amounts of strontium are derived from a fan draining a carbonate terrane have strontium component. Although much evidence points to an eolian source for at least some of the strontium in the pedogenic carbonates near Yucca Mountain, an additional component or past variation of strontium composition in the eolian source is required to model the pedogenic carbonate system

  3. Strontium isotope geochemistry of soil and playa a deposits near Yucca Mountain, Nevada

    International Nuclear Information System (INIS)

    Marshall, B.D.; Mahan, S.A.

    1994-01-01

    The isotopic composition of strontium contained in the carbonate fractions of soils provides an excellent tracer which can be used to test models for their origin. This paper reports data on surface coatings and cements, eolian sediments, playas and alluvial fan soils which help to constrain a model for formation of the extensive calcretes and fault infilling in the Yucca Mountain region. The playas contain carbonate with a wide range of strontium compositions; further work will be required to fully understand their possible contributions to the pedogenic carbonate system. Soils from an alluvial fan to the west of Yucca Mountain show that only small amounts of strontium are derived from weathering of silicate detritus. However, calcretes from a fan draining a carbonate terrane have strontium compositions dominated locally by the limestone strontium component. Although much evidence points to an eolian source for at least some of the strontium in the pedogenic carbonates near Yucca Mountain, an additional component or past variation of strontium composition in the eolian source is required to model the pedogenic carbonate system

  4. Elemental geochemistry and strontium-isotope stratigraphy of Cenomanian to Santonian neritic carbonates in the Zagros Basin, Iran

    Science.gov (United States)

    Navidtalab, Amin; Rahimpour-Bonab, Hossain; Huck, Stefan; Heimhofer, Ulrich

    2016-12-01

    A Neo-Tethyan upper Cenomanian-Santonian neritic carbonate ramp succession (Sarvak and Ilam formations), drilled in the Zagros Basin in southwest Iran, was investigated via detailed sedimentology, microfacies analysis, elemental geochemistry and Sr-isotope stratigraphy (SIS). The succession contains two exposure surfaces, which are known as the CT-ES and mT-ES (Cenomanian-Turonian and middle Turonian, respectively), and associated prominent negative carbon-isotope excursions that represent important regional stratigraphic marker horizons. Precise knowledge about the onset of platform exposure and the duration of the exposure-related hiatus, however, is currently lacking due to a rather low-resolved shallow-water biostratigraphic framework and a bulk carbonate carbon-isotope pattern that clearly differs from global Late Cretaceous reference curves. Therefore, the existing bio-chemostratigraphic framework was complemented by bulk carbonate strontium-isotope stratigraphy (SIS). As bulk carbonate material is in particular prone to diagenetic alteration, a careful selection of least altered samples has been carried out by means of elemental geochemistry and petrography. In contrast to what could be expected, the meteoric alteration of limestones beneath both exposure surfaces is not clearly expressed by increasing iron and manganese and coeval decreasing strontium contents. On the contrary, the impact of meteoric diagenesis is well illustrated via pronounced increases in Rb concentrations and concomitant prominent positive shifts to radiogenic strontium-isotope values, an observation that clearly reflects the decay of continentally derived 87Rb into 87Sr. Rubidium corrected strontium-isotope values place the CT-ES around the Cenomanian-Turonian boundary and point to an exposure duration of less than 0.4 Myr. This rather short-term CT-ES related hiatus is supported by petrographic evidence, which indicates a youth karstification stage of strata beneath the CT

  5. Strontium isotope geochemistry of alluvial groundwater: a tracer for groundwater resources characterisation

    Directory of Open Access Journals (Sweden)

    P. Négrel

    2004-01-01

    Full Text Available This study presents strontium isotope and major ion data of shallow groundwater and river water from the Ile du Chambon catchment, located on the Allier river in the Massif Central (France. There are large variations in the major-element contents in the surface- and groundwater. Plotting of Na vs. Cl contents and Ca, Mg, NO3, K, SO4, HCO3, Sr concentrations reflect water–rock interaction (carbonate dissolution for Ca, Mg, HCO3 and Sr because the bedrock contains marly limestones, agricultural input (farming and fertilising and sewage effluents (for NO3, K, SO4, although some water samples are unpolluted. Sr contents and isotope ratios (87Sr/86Sr vary from 0.70892 to 0.71180 along the hydrological cycle in the groundwater agree with previous work on groundwater in alluvial aquifers in the Loire catchment. The data plot along three directions in a 87Sr/86Sr v. 1/Sr diagram as a result of mixing, involving at least three geochemical signatures–Allier river water, and two distinct signatures that might be related to different water-rock interactions in the catchment. Mixing proportions are calculated and discussed. The alluvial aquifer of the Ile du Chambon catchment is considered, within the Sr isotope systematic, in a larger scheme that includes several alluvial aquifers of the Loire Allier catchment. Keywords: : Loire river, major and trace elements, Sr isotopic ratio, alluvial aquifer, hydrology

  6. Strontium isotope geochemistry of groundwater affected by human activities in Nandong underground river system, China

    Energy Technology Data Exchange (ETDEWEB)

    Jiang Yongjun, E-mail: jiangjyj@swu.edu.cn [School of Geographical Sciences, Southwest University, Chongqing 400715 (China)] [Institute of Karst Environment and Rock Desertification Rehabilitation, Chongqing 400715 (China)

    2011-03-15

    Research highlights: {yields} Spatio-temporal variations of Sr concentrations and Sr isotopic composition of groundwater were investigated in a karst underground river system. {yields} Agricultural fertilizers and sewage effluents significantly modified the natural Sr isotopic signature of karst groundwater. {yields} Sr in the carbonate aquifers was relatively non-radiogenic, with low Sr concentrations, while anthropogenic Sr correlated with agricultural fertilizers and sewage effluents was relatively radiogenic, with higher Sr concentrations. {yields} {sup 87}Sr/{sup 86}Sr ratios can provide key information for natural and anthropogenic sources in karst groundwater. - Abstract: The Nandong Underground River System (NURS) is located in a typical karst area dominated by agriculture in SE Yunnan Province, China. Groundwater plays an important role in the social and economical development in the area. The effects of human activities (agriculture and sewage effluents) on the Sr isotope geochemistry were investigated in the NURS. Seventy-two representative groundwater samples, which were collected from different aquifers (calcite and dolomite), under varying land-use types, both in summer and winter, showed significant spatial differences and slight seasonal variations in Sr concentrations and {sup 87}Sr/{sup 86}Sr ratios. Agricultural fertilizers and sewage effluents significantly modified the natural {sup 87}Sr/{sup 86}Sr ratios signature of groundwater that was otherwise dominated by water-rock interaction. Three major sources of Sr could be distinguished by {sup 87}Sr/{sup 86}Sr ratios and Sr concentrations in karst groundwater. Two sources of Sr are the Triassic calcite and dolomite aquifers, where waters have low Sr concentrations (0.1-0.2 mg/L) and low {sup 87}Sr/{sup 86}Sr ratios (0.7075-0.7080 and 0.7080-0.7100, respectively); the third source is anthropogenic Sr from agricultural fertilizers and sewage effluents with waters affected having radiogenic {sup 87

  7. Strontium isotope geochemistry of groundwater in the central part of the Dakota (Great Plains) aquifer, USA

    International Nuclear Information System (INIS)

    Gosselin, David C.; Edwin Harvey, F.; Frost, Carol; Stotler, Randy; Allen Macfarlane, P.

    2004-01-01

    The Dakota aquifer of the central and eastern Great Plains of the United States is an important source of water for municipal supplies, irrigation and industrial use. Although the regional flow system can be characterized generally as east to northeasterly from the Rocky Mountains towards the Missouri River, locally the flow systems are hydrologically complex. This study uses Sr isotopic data from groundwater and leached aquifer samples to document the complex subsystems within the Dakota aquifer in Nebraska and Kansas. The interaction of groundwater with the geologic material through which it flows has created spatial patterns in the isotopic measurements that are related to: long-term water-rock interaction, during which varying degrees of isotopic equilibrium between water and rock has been achieved; and the alteration of NaCl fluids by water-rock interaction. Specifically, Sr isotopic data distinguish brines from Kansas and western Nebraska from those in eastern Nebraska: the former are interpreted to reflect interaction with Permian rocks, whereas the latter record interaction with Pennsylvanian rocks. The Sr isotopic composition of groundwater from other parts of Nebraska and Kansas are a function of the dynamic interaction between groundwater and unlithified sediments (e.g., glacial till and loess), followed by interaction with oxidized and unoxidized sediments within the Dakota Formation. This study illustrates the power of combining Sr chemistry with more conventional geochemical data to obtain a more complete understanding of groundwater flow systems within regional aquifer systems where extensive monitoring networks do not exist

  8. Geochemistry of silicon isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Tiping; Li, Yanhe; Gao, Jianfei; Hu, Bin [Chinese Academy of Geological Science, Beijing (China). Inst. of Mineral Resources; Jiang, Shaoyong [China Univ. of Geosciences, Wuhan (China).

    2018-04-01

    Silicon is one of the most abundant elements in the Earth and silicon isotope geochemistry is important in identifying the silicon source for various geological bodies and in studying the behavior of silicon in different geological processes. This book starts with an introduction on the development of silicon isotope geochemistry. Various analytical methods are described and compared with each other in detail. The mechanisms of silicon isotope fractionation are discussed, and silicon isotope distributions in various extraterrestrial and terrestrial reservoirs are updated. Besides, the applications of silicon isotopes in several important fields are presented.

  9. SHELL ISOTOPE GEOCHEMISTRY

    African Journals Online (AJOL)

    ABSTRACT: The land snail Limicolaria kambeul chudeaui Germain was collected ... Key words/phrases: Ethiopia, isotope geochemistry, Lake Tilo, Limicolaria .... 1984), (c) 6'80 values of precipitation at Addis Ababa, with i 1 S.D. bars for the .... (breakfast cereal), deionised water and cuttlefish bone, the carbon and oxygen.

  10. Calcium stable isotope geochemistry

    Energy Technology Data Exchange (ETDEWEB)

    Gausonne, Nikolaus [Muenster Univ. (Germany). Inst. fuer Mineralogie; Schmitt, Anne-Desiree [Strasbourg Univ. (France). LHyGeS/EOST; Heuser, Alexander [Bonn Univ. (Germany). Steinmann-Inst. fuer Geologie, Mineralogie und Palaeontologie; Wombacher, Frank [Koeln Univ. (Germany). Inst. fuer Geologie und Mineralogie; Dietzel, Martin [Technische Univ. Graz (Austria). Inst. fuer Angewandte Geowissenschaften; Tipper, Edward [Cambridge Univ. (United Kingdom). Dept. of Earth Sciences; Schiller, Martin [Copenhagen Univ. (Denmark). Natural History Museum of Denmark

    2016-08-01

    This book provides an overview of the fundamentals and reference values for Ca stable isotope research, as well as current analytical methodologies including detailed instructions for sample preparation and isotope analysis. As such, it introduces readers to the different fields of application, including low-temperature mineral precipitation and biomineralisation, Earth surface processes and global cycling, high-temperature processes and cosmochemistry, and lastly human studies and biomedical applications. The current state of the art in these major areas is discussed, and open questions and possible future directions are identified. In terms of its depth and coverage, the current work extends and complements the previous reviews of Ca stable isotope geochemistry, addressing the needs of graduate students and advanced researchers who want to familiarize themselves with Ca stable isotope research.

  11. Calcium stable isotope geochemistry

    International Nuclear Information System (INIS)

    Gausonne, Nikolaus; Schmitt, Anne-Desiree; Heuser, Alexander; Wombacher, Frank; Dietzel, Martin; Tipper, Edward; Schiller, Martin

    2016-01-01

    This book provides an overview of the fundamentals and reference values for Ca stable isotope research, as well as current analytical methodologies including detailed instructions for sample preparation and isotope analysis. As such, it introduces readers to the different fields of application, including low-temperature mineral precipitation and biomineralisation, Earth surface processes and global cycling, high-temperature processes and cosmochemistry, and lastly human studies and biomedical applications. The current state of the art in these major areas is discussed, and open questions and possible future directions are identified. In terms of its depth and coverage, the current work extends and complements the previous reviews of Ca stable isotope geochemistry, addressing the needs of graduate students and advanced researchers who want to familiarize themselves with Ca stable isotope research.

  12. Niobium-Thorium-Strontium-Rare Earth Element Mineralogy and Preliminary Sulphur Isotope Geochemistry of the Eaglet Property, East-Central British Columbia (NTS 093A/10W)

    Czech Academy of Sciences Publication Activity Database

    Hora, Z. D.; Langrová, Anna; Pivec, Edvín; Žák, Karel

    2010-01-01

    Roč. 2009, č. 1 (2010), s. 93-96 ISSN 0381-243X Institutional research plan: CEZ:AV0Z30130516 Keywords : fluorite * celestite * pyrochlore * thorite * titanbetafite * bastnaesite * sulphur isotopes * Eaglet deposit * MINFILE 093A46 Subject RIV: DD - Geochemistry http://www.empr.gov.bc.ca/Mining/Geoscience/PublicationsCatalogue/Fieldwork/Documents/2009/08_Hora_2009.pdf

  13. Strontium geochemistry and carbon and oxygen isotopic compositions of Lower Proterozoic dolomite and calcite marbles from the Marmorilik Formation, West Greenland

    International Nuclear Information System (INIS)

    Garde, A.A.

    1979-01-01

    The Marmorilik Formation, Rinkian mobile belt, West Greenland, is a large, Lower Proterozoic carbonate-rock sequence, deformed and metamorphosed under greenschist to amphibolite facies conditions. The pre-deformation thickness of the sequence is at least 2000 m, with about 1400 m of dolomite marble and 350 m of calcite marble. Strontium contents of forty-two dolomite and calcite marbles range from 30 to 100 ppm and 300 to 800 ppm, respectively, whereas samples with calcite of secondary origin have strontium contents between 80 ppm and 200 ppm. Carbon and oxygen isotope ratios were determined for forty calcite and dolomite marbles as -0.2+-1.0 per 1000 delta 13 C and -9.9+-1.5 per 1000 delta 18 O (vs. PDB) and are compatible with the isotopic compositions of unmetamorphosed carbonates of similar age. Calcite from eight calciumsilicate rocks, breccias and calcite veins is significantly more negative in delta 13 C and delta 18 O. Five 13 C analyses of graphite in marble range from -9.6 to -14 per 1000. Possible post-depositional changes in the strontium content and carbon and oxygen isotope compositions are discussed. It is concluded that (a) the calcite marbles are not dedolomites and are therefore of primary origin, (b) the delta 13 C and delta 18 O values of the marbles are primary or diagenetic (i.e., pre-metamorphic), and (c) the isotopic composition of the graphite is compatible with, though not necessarily evidence for, a biogenic origin. (Auth.)

  14. Strontium isotopic and trace element geochemistry of the saddle mountains and Grande Ronde Basalts of the Columbia River Basalt Group

    International Nuclear Information System (INIS)

    Nelson, D.O.

    1980-01-01

    The Columbia River Basalt (CRB) group displays significant variations in major and trace element and Sr isotopic compositions. These compositions reflect complex and variable origins for the CRB magmas. Among the most varied is the Saddle Mountains Basalt (SMB) in which Sr ratios vary from 0.7078 to 0.7147 +- 0.002. The higher ratios reflect contamination through consistent correlations with major element compositions. Modeling suggests contamination by assimilation of 4.4 to 9.4 wt % of radiogenic crustal rocks. High delta 18 O values (up to +7.68 per mil) support the model. Age and field relations suggest that the contamination flowrocks are not the result of progressive contamination of a single magma, but rather reflect the contamination of independent magmas during this ascent

  15. High-resolution stratigraphy with strontium isotopes.

    Science.gov (United States)

    Depaolo, D J; Ingram, B L

    1985-02-22

    The isotopic ratio of strontium-87 to strontium-86 shows no detectable variation in present-day ocean water but changes slowly over millions of years. The strontium contained in carbonate shells of marine organisms records the ratio of strontium-87 to strontium-86 of the oceans at the time that the shells form. Sedimentary rocks composed of accumulated fossil carbonate shells can be dated and correlated with the use of high precision measurements of the ratio of strontium-87 to strontium-86 with a resolution that is similar to that of other techniques used in age correlation. This method may prove valuable for many geological, paleontological, paleooceanographic, and geochemical problems.

  16. Isotopic geochemistry at Wairakei

    International Nuclear Information System (INIS)

    Stewart, M.K.

    1985-12-01

    Deuterium measurements on geothermal water at Wairakei are consistent with the water being derived from rainfall which has percolated down from the surface. The oxygen-18 content, however, is enriched compared to average rainfall. This 18 O shift is due to isotopic exchange between water and rock at greater-than-explored depths. The magnitude of the shift implied that the mass ration (W/R) of water that has passed through the system (W) to the rock it has exchanged with (R) is about 1 assuming open (i.e. single-pass) conditions. (The ratio is about 2 if it has been a closed system, but this is thought to be less likely). The residence time of water underground cannot be determined from tritium and carbon-14 measurements at present, but arguments based on the argon isotope and deuterium contents suggest mean residence times of a few tens of thousand years. The water-rock ratio and large natural outflow of thermal water prior to exploitation are consistent with this. The 18 O content of the water has changed only slightly, and the D content not at all, during exploitation at Wairakei (measurements from 1963, 1974 and 1981). An initial tendency for the 18 O to increase because of steam loss (also shown more clearly by chloride), has been followed by decrease of 18 O (and chloride) because of dilution with infiltrating near-surface water in parts of the field

  17. Isotope exchange of strontium and molybdate ions in strontium polymolybdates

    International Nuclear Information System (INIS)

    Atun, G.

    2002-01-01

    The heterogeneous isotopic exchange reactions in strontium polymolybdates of Sr 2+ and MoO 4 2- ions in the strontium nitrate and sodium molybdate solutions have been studied using 90 Sr and 99 Mo as tracers. Electrometric methods have been used to study the compositions of strontium molybdates obtained by adding strontium chloride to a progressively acidified solution of sodium molybdate. It has been found that the exchange fraction increases with increasing chain length of strontium polymolybdate. The exchange equilibrium constant (K ex ) has been calculated between 298 and 348 K as well as ΔG deg, ΔH deg and ΔS deg. The results indicate that Sr 2+ cations have a much higher affinity for exchangers than MoO 4 2- anions. By fitting the data to the Dubinin-Radushkevich (D-R) isotherm it has been shown that the exchange capacity (X m ) for both ions is affected by the ion adsorption process at low temperatures and by the ion exchange process at high temperatures. At high concentrations, the recrystallization process contributes to on the cation exchange but is ineffective on the anion exchange mechanism. (author)

  18. Radiogenic isotope geochemistry of sedimentary and aquatic systems

    International Nuclear Information System (INIS)

    Stille, P.; Shields, G.

    1997-01-01

    The following topics are discussed: Basic principles of isotopic geochemistry; weathering; isotopic geochemistry of river water; isotopic geochemistry in the environment; isotopic composition of seawater past and present (Sr, Nd, Pb, Os, Ce); isotope geochemistry of detrital and authigenic clay minerals in marine sediemnts (Rb-Sr, K-Ar, O); the Sm-N isotope system in detrital and authigenic argillaceous sediments. (SR), provided they are of exceptional interest and focused on a single topic. (orig./SR)

  19. Radiogenic isotope geochemistry of sedimentary and aquatic systems

    Energy Technology Data Exchange (ETDEWEB)

    Stille, P.; Shields, G. [Centre National de la Recherche Scientifique (CNRS), 67 - Strasbourg (France). Centre de Sedimentologie et Geochimie de la Surface

    1997-12-31

    The following topics are discussed: Basic principles of isotopic geochemistry; weathering; isotopic geochemistry of river water; isotopic geochemistry in the environment; isotopic composition of seawater past and present (Sr, Nd, Pb, Os, Ce); isotope geochemistry of detrital and authigenic clay minerals in marine sediemnts (Rb-Sr, K-Ar, O); the Sm-N isotope system in detrital and authigenic argillaceous sediments. (SR), provided they are of exceptional interest and focused on a single topic. (orig./SR)

  20. Strontium isotope stratigraphy of the Pelotas Basin

    Energy Technology Data Exchange (ETDEWEB)

    Zerfass, Geise de Santana dos Anjos, E-mail: geise.zerfass@petrobras.com.br [Petroleo Brasileiro S.A. (PETROBRAS/CENPES/PDGEO/BPA), Rio de Janeiro, RJ (Brazil). Centro de Pesquisas e Desenvolvimento Leopoldo Americo Miguez de Mello; Chemale Junior, Farid, E-mail: fchemale@unb.br [Universidade de Brasilia (UnB), DF (Brazil). Instituto de Geociencias; Moura, Candido Augusto Veloso, E-mail: candido@ufpa.br [Universidade Federal do Para (UFPA), Belem, PA (Brazil). Centro de Geociencias. Dept. de Geoquimica e Petrologia; Costa, Karen Badaraco, E-mail: karen.costa@usp.br [Instituto Oceanografico, Sao Paulo, SP (Brazil); Kawashita, Koji, E-mail: koji@usp.br [Unversidade de Sao Paulo (USP), SP (Brazil). Centro de Pesquisas Geocronologicas

    2014-07-01

    Strontium isotope data were obtained from foraminifera shells of the Pelotas Basin Tertiary deposits to facilitate the refinement of the chronostratigraphic framework of this section. This represents the first approach to the acquisition of numerical ages for these strata. Strontium isotope stratigraphy allowed the identification of eight depositional hiatuses in the Eocene-Pliocene section, here classified as disconformities and a condensed section. The reconnaissance of depositional gaps based on confident age assignments represents an important advance considering the remarkably low chronostratigraphic resolution in the Cenozoic section of the Pelotas Basin. The recognition of hiatuses that match hiatuses is based on biostratigraphic data, as well as on global events. Furthermore, a substantial increase in the sedimentation rate of the upper Miocene section was identified. Paleotemperature and productivity trends were identified based on oxygen and carbon isotope data from the Oligocene-Miocene section, which are coherent with worldwide events, indicating the environmental conditions during sedimentation. (author)

  1. On models in the geochemistry of isotopes

    International Nuclear Information System (INIS)

    Wetzel, K.

    1978-01-01

    Models are playing an increasing role in the deepening of our understanding of the laws of occurrence of stable and radioactive isotopes in nature. The properties of concrete global and regional models of the geochemistry of isotopes are derived from a general model characterizing the cycling of chemical elements and their isotopes in nature. The importance of global models as well as the relationships between global and regional models are considered. The introduction of a parameter describing the velocity of both mass and isotope transfer, taking into consideration the global resources, renders possible the linkage of global models with regional ones. (author)

  2. Handbook of environmental isotope geochemistry

    Energy Technology Data Exchange (ETDEWEB)

    Baskaran, Mark (ed.) [Wayne State Univ., Detroit, MI (United States). Dept. Geology

    2011-07-01

    Applications of radioactive and stable isotopes have revolutionized our understanding of the Earth and near-earth surface processes. The utility of the isotopes are ever-increasing and our sole focus is to bring out the applications of these isotopes as tracers and chronometers to a wider audience so that they can be used as powerful tools to solve environmental problems. New developments in this field remain mostly in peer-reviewed journal articles and hence our goal is to synthesize these findings for easy reference for students, faculty, regulators in governmental and non-governmental agencies, and environmental companies. While this volume maintains its rigor in terms of its depth of knowledge and quantitative information, it contains the breadth needed for wide variety problems and applications in the environmental sciences. This volume presents all of the newer and older applications of isotopes pertaining to the environmental problems in one place that is readily accessible to readers. This book not only has the depth and rigor that is needed for academia, but it has the breadth and case studies to illustrate the utility of the isotopes in a wide variety of environments (atmosphere, oceans, lakes, rivers and streams, terrestrial environments, and sub-surface environments) and serves a large audience, from students and researchers, regulators in federal, state and local governments, and environmental companies. (orig.)

  3. Kinetics of isotopic exchange between strontium polymolybdate and strontium ions in aqueous solution

    International Nuclear Information System (INIS)

    Atun, Gulten; Bilgin, Binay; Kilislioglu, Ayben

    2002-01-01

    A heterogeneous isotopic exchange reaction of strontium polymolybdate in strontium chloride solution was studied using 90 Sr as a tracer. The effects of low and high strontium chloride concentration on the rate and mechanism of the isotopic exchange reaction were investigated. It was found that, at high concentrations, the rate is independent of strontium concentration, but, at low concentrations, the rate is proportional to the strontium concentration. These results support a hypothesis that, at low concentrations, the rate is controlled by film diffusion, whereas at high concentrations it is controlled by particle diffusion. Experiments were performed at 293, 303 and 313 K. Activation energy of isotopic exchange reaction and thermodynamic parameters ΔH*, ΔS*, and ΔG* were calculated using the Arrhenius and Eyring equations. The results also indicated that recrystallization is a predominant factor in the present exchange reaction

  4. Kinetics of isotopic exchange between strontium polymolybdate and strontium ions in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Atun, Gulten E-mail: gultena@istanbul.edu.tr; Bilgin, Binay; Kilislioglu, Ayben

    2002-06-01

    A heterogeneous isotopic exchange reaction of strontium polymolybdate in strontium chloride solution was studied using {sup 90}Sr as a tracer. The effects of low and high strontium chloride concentration on the rate and mechanism of the isotopic exchange reaction were investigated. It was found that, at high concentrations, the rate is independent of strontium concentration, but, at low concentrations, the rate is proportional to the strontium concentration. These results support a hypothesis that, at low concentrations, the rate is controlled by film diffusion, whereas at high concentrations it is controlled by particle diffusion. Experiments were performed at 293, 303 and 313 K. Activation energy of isotopic exchange reaction and thermodynamic parameters {delta}H*, {delta}S*, and {delta}G* were calculated using the Arrhenius and Eyring equations. The results also indicated that recrystallization is a predominant factor in the present exchange reaction.

  5. Strontium stable isotope behaviour accompanying basalt weathering

    Science.gov (United States)

    Burton, K. W.; Parkinson, I. J.; Gíslason, S. G. R.

    2016-12-01

    The strontium (Sr) stable isotope composition of rivers is strongly controlled by the balance of carbonate to silicate weathering (Krabbenhöft et al. 2010; Pearce et al. 2015). However, rivers draining silicate catchments possess distinctly heavier Sr stable isotope values than their bedrock compositions, pointing to significant fractionation during weathering. Some have argued for preferential release of heavy Sr from primary phases during chemical weathering, others for the formation of secondary weathering minerals that incorporate light isotopes. This study presents high-precision double-spike Sr stable isotope data for soils, rivers, ground waters and estuarine waters from Iceland, reflecting both natural weathering and societal impacts on those environments. The bedrock in Iceland is dominantly basaltic, d88/86Sr ≈ +0.27, extending to lighter values for rhyolites. Geothermal waters range from basaltic Sr stable compositions to those akin to seawater. Soil pore waters reflect a balance of input from primary mineral weathering, precipitation and litter recycling and removal into secondary phases and vegetation. Rivers and ground waters possess a wide range of d88/86Sr compositions from +0.101 to +0.858. Elemental and isotope data indicate that this fractionation primarily results from the formation or dissolution of secondary zeolite (d88/86Sr ≈ +0.10), but also carbonate (d88/86Sr ≈ +0.22) and sometimes anhydrite (d88/86Sr ≈ -0.73), driving the residual waters to heavier or lighter values, respectively. Estuarine waters largely reflect mixing with seawater, but are also be affected by adsorption onto particulates, again driving water to heavy values. Overall, these data indicate that the stability and nature of secondary weathering phases, exerts a strong control on the Sr stable isotope composition of silicate rivers. [1] Krabbenhöft et al. (2010) Geochim. Cosmochim. Acta 74, 4097-4109. [2] Pearce et al. (2015) Geochim. Cosmochim. Acta 157, 125-146.

  6. Source of Lake Vostok Cations Constrained with Strontium Isotopes

    Directory of Open Access Journals (Sweden)

    William Berry Lyons

    2016-08-01

    Full Text Available Lake Vostok is the largest sub-glacial lake in Antarctica. The primary source of our current knowledge regarding the geochemistry and biology of the lake comes from the analysis of refrozen lake water associated with ice core drilling. Several sources of dissolved ions and particulate matter to the lake have been proposed, including materials from the melted glacier ice, the weathering of underlying geological materials, hydrothermal activity and underlying, ancient evaporitic deposits. A sample of Lake Vostok Type 1 accretion ice has been analyzed for its 87Sr/86Sr signature as well as its major cation and anion and Sr concentrations. The strontium isotope ratio of 0.71655 and the Ca/Sr ratio in the sample strongly indicate that the major source of the Sr is from aluminosilicate minerals from the continental crust. These data imply that at least a portion of the other cations in the Type 1 ice also are derived from continental crustal materials and not hydrothermal activity, the melted glacier ice, or evaporitic sources.

  7. Strontium isotopic stratigraphy utilizing authigenic dolomites in hemipelagic sediments

    Energy Technology Data Exchange (ETDEWEB)

    Baker, P.A. (Duke Univ., Durham, NC (USA)); Kastner, M. (Scripps Institute of Oceanography, La Jolla, CA (USA)); Elderfield, H. (Univ. of Cambridge (England))

    1990-05-01

    Authigenic dolomites commonly occur in organic-rich, continental margin marine sediments. These dolomites play a key role in the age dating of stratigraphic sections. The dolomites often are the only lithology amenable to paleomagnetic stratigraphy; they preserve siliceous microfossils against diagenetic; recrystallization, and provide useful strontium isotopic stratigraphic ages. Several potential sources of error frequently are unique to the use of authigenic dolomites in the strontium isotope methods. (1) The dolomites occur as cements of the host lithology, hence, they are not a pure phase. Potentially important contaminants during analysis include gypsum clay minerals, feldspars, and iron and manganese oxides. Strontium may occur as a structural substituent ion in these minerals or as a surface-adsorbed ion. Various leaching techniques have been tested to isolate dolomitic strontium. Purer dolomites and strontium-enriched dolomites often can be selected to ease these problems. (2) The dolomites form after the deposition of the host sediment, therefore, they record the diagenetic age not the depositional age. The stable isotopic composition of the dolomites can aid in selection of early formed samples. (3) The dolomites record pore-water strontium isotope compositions, not seawater isotopic compositions. This problem is also minimized by choosing dolomites formed near the sediment-water interface. (4) The dolomites formed near the sediment-water interface originated as rotodolomites and undergo subsequent burial diagenesis, creating a potential for later strontium isotope exchange. This problem is minimized by selecting fresh samples from the interior of nearly impermeable beds and nodules. Results from the Miocene Monterey Formation of California and from the Eocene through Pliocene Pisco basin of Peru show that authigenic dolomites can provide useful strontium isotopic age estimates.

  8. 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...

  9. Stable strontium isotopic ratios from archaeological organic remains from the Thorsberg peat bog

    DEFF Research Database (Denmark)

    Nosch, Marie-Louise Bech; von Carnap-Bornheim, Claus; Grupe, Gisela

    2007-01-01

    Pilot study analysing stable strontium isotopic ratios from Iron Age textile and leather finds from the Thorsberg peat bog.......Pilot study analysing stable strontium isotopic ratios from Iron Age textile and leather finds from the Thorsberg peat bog....

  10. Application of environmental isotope tracing technology to geothermal geochemistry

    International Nuclear Information System (INIS)

    Shang Yingnan

    2006-01-01

    This paper reviews the recent application and development of environmental isotope tracing technology to geothermal geochemistry in the following aspects: gas isotopes (He, C) tracing of warm springs; H, O isotope tracing on the origin and cause of geothermal water, environmental isotope dating of geothermal water, and the advantage of excess parameter of deuterium (d) in geothermal research. The author also suggests that isotope method should combine with other geological methods to expand its advantage. (authors)

  11. In-situ Strontium Isotopes Analysis on Single Conodont Apatite by LA-MC-ICP-MS

    Science.gov (United States)

    Zhao, L.; Zhang, L.; Chen, Z. Q.; Ma, D.; Qiu, H.; Lv, Z.; Hu, Z.; Wang, F.

    2014-12-01

    Strontium isotope played an important role in stratigraphic chronology and sedimentary geochemistry research (McArthur et al., 2001). Conodonts is a kind of extinct species of marine animals and widely distributed in marine sediments all over the world. Rich in radiogenic Sr contents and difficulty to be affected during diagenesis alteration makes conodonts a good choice in seawater Sr isotope composition studies (John et al., 2008). Conodont samples were collected from 24th to 39th layer across Permian-Triassic boundary at Meishan D section (GSSP), Zhejiang Province, South China (Yin et al., 2001). Conodonts was originated from fresh limestone and only conodont elements with CAIextinction events during the Permian-Triassic transition. Our study also makes is possible for high resolution 87Sr/ 86Sr ratio testing on the single conodont apatite and riched the in-situ studies on the conodont apatite, which of great significance for the future conodont Sr isotope research (Zhao et al., 2009; Zhao et al., 2013). Keywords: Conodonts, Strontium isotope, LA-MC-ICP-MS, Permian-Triassic transition, Meishan D section [1] John et al., 2008 3P[2] McArthur et al., 2001 J. of Geology [3] Yin et al., 2001 Episodes [4] Zhao et al., 2009 Earth Science J. of CUG [5] Zhao et al., 2013 GPC.

  12. Stable isotope geochemistry. 3. rev. and enl. ed.

    International Nuclear Information System (INIS)

    Hoefs, J.

    1987-01-01

    Stable Isotope Geochemistry is an authoritative book comprising theoretical and experimental principles; surveying important fractionation mechanisms affecting the most important elements; discussing the natural variations of geologically important reservoirs. This updated 3rd edition, with a completely rewritten and extended main part, contains two new chapters on stable isotope composition of mantle material and on changes of the ocean during the geological past. (orig.)

  13. The geochemistry of stable chlorine and bromine isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Eggenkamp, Hans [Onderzock and Beleving, Bussum (Netherlands)

    2014-11-01

    First book solely dedicated to the geochemistry of chlorine and bromine isotopes. Detailed description of analytical techniques, including their advantages and disadvantages. Indication of research fields where measurement of these isotopes is especially useful. This book provides detailed information on the history, analysis and applications of chlorine and bromine isotope geochemistry. Chlorine and bromine are geochemically unique as they prefer to exist as single charged negative ions. For this reason isotope fractionation reflects mostly processes that are not related to changes in the redox state and this fractionation is generally modest. The book will describe the processes that are most easily detected using these isotopes. Also isotope variations, and processes that cause them, measured in oxidised species such as perchlorates and in organic molecules will be described in this book.

  14. Stable isotope geochemistry : definitions, terminology, measurement and some applications

    International Nuclear Information System (INIS)

    Faure, K.

    2005-01-01

    In 1936, Alfred Nier produced the first precise measurement of isotope abundance ratios and his design still remains the basis of stable isotope mass spectrometry. With this gift from the physicists for routine measurement of isotope ratios, earth scientists began to explore the natural variations of isotopes. Thus began a new era in geoscience research with the hydrological cycle and marine palaeoclimatic research being the first topics to be investigated. Stable isotope measurements have been applied to many fundamental problems in geochemistry, petrology and paleoclimatology, as well as related fields in archaeology, anthropology, physical chemistry, biology and forensic sciences. (author). 52 refs., 11 figs., 2 tabs

  15. Practical aspects of the environmental behavior of strontium isotopes

    International Nuclear Information System (INIS)

    Madelmont, Claude; Bittel, Robert; Daburon, Francois.

    1977-03-01

    The practical aspects of contamination patterns of the food chain by strontium isotopes are reviewed - plants with special emphasis on the consequences of irrigation (contamination level at equilibrium); dairy products and the adjustement of a general model to regional conditions (a table of quantitative parameters for some French regions is included); marine and freshwater products. One should keep in mind that transfer parameters may change with time and cannot be assessed definitively [fr

  16. Stable isotope geochemistry : definitions, terminology, measurement and some applications

    International Nuclear Information System (INIS)

    Faure, K.

    2004-01-01

    Stable isotope measurements have been applied to many fundamental problems in geochemistry, petrology, and paleoclimatology, as well as related fields in archaeology, anthropology, physical chemistry, biology and forensic sciences. These applications can be broadly classified into four main types: thermometry, tracers, reaction mechanisms and chemostratigraphy. 52 refs., 11 figs., 2 tabs

  17. Seawater strontium isotopes at the Cretaceous-Tertiary boundary

    Science.gov (United States)

    Macdougall, J. D.; Martin, E.

    1988-01-01

    Anomalously high values of Seawater Sr-87/Sr-86 near the Cretaceous-Tertiary (K-T) boundary have been reported. However, few of the data from the literature are from a single continuous section, and perhaps the most complete study of the boundary region, from a shallow marine limestone sequence in Alabama, showed elevated Sr-87/Sr-86 but no pronounced spike. Thus, in order to investigate the cause of the change in strontium isotopic composition, it is important to determine the exact nature and magnitude of the increase by studying in detail continuous sections through the boundary. If there is indeed a Sr isotope spike at the K-T boundary, it requires the addition of a large amount of radiogenic Sr to the oceans over a short time period, a phenomenon that may be linked to other large-scale environmental disturbances which occurred at that time. In order to address this question, a high-resolution strontium isotope study of foraminifera from three Deep Sea Drilling Project (DSDP) cores which recovered the K-T boundary section: Site 356 in the South Atlantic, Site 384 in the North Atlantic and Site 577 from the Shatsky Rise in the Pacific was initiated. The isotope measurements are being made on either single or small numbers of forams carefully picked and identified and in most cases examined by SEM before analysis. Because this work is not yet complete, conclusions drawn here must be viewed as tentative. They are briefly discussed.

  18. Geochemistry, age and strontium isotope composition of late tertiary and quaternary basalts and andesites in western Nevada and their relation to geothermal potential. Final report, October 1, 1982-December 31, 1983

    Energy Technology Data Exchange (ETDEWEB)

    Fultz, L.A.; Bell, E.J.; Trexler, D.T.

    1984-01-01

    This research was undertaken to characterize the late Cenozoic volcanic rocks associated with active geothermal systems in west-central Nevada. Petrographic and microprobe, geochemical and isotopic analysis and age dating techniques were used to characterize these young volcanic rocks. These data were combined with the limited data previously reported in the literature on these same volcanic areas to interpret their petrogenesis. The overall characterization resulted from integrating the petrogenesis with a structural-tectonic model of the region. Potassium-argon isotopic ages ranging up to 14 million years were determined for eight localities within the Reno 1 x 2/sup 0/ study region. These ages are consistent with the morphology of the volcanic landforms, the active geothermal systems associated with them, and with other isotopic ages reported in the literature for these and similar rocks within the study region. Petrographic analysis of hand specimens and thin-sections indicated mineralogic assemblages of the respective rock types and specific mineral textures and phenocryst compositions and characteristics. These identifications were further substantiated by microprobe analysis of selected phenocrysts and groundmass phases. Classification of the respective rock types was also based on chemical composition and normative calculations using the program PETCAL. Basaltic andesites are identified and described for Steamboat Hills, Table Mountain, Silver Springs, Churchill Butte, Cleaver Peak, Desert Peak and Carson City sites.

  19. Determining the sources of calcium for migratory songbirds using stable strontium isotopes.

    Science.gov (United States)

    Blum, Joel D; Taliaferro, E Hank; Holmes, Richard T

    2001-02-01

    We investigated natural variations in the stable isotopic composition of strontium (a surrogate for calcium) in the bones of a single species of breeding migratory songbird, as well as in their eggshells, egg contents, and food sources. We use this information to determine the sources of calcium to these migratory songbirds and their offspring. Samples were collected from two locations in the northeastern USA (Hubbard Brook, NH, and Downer Forest, VT.) that differed in soil geochemistry. The mean 87 Sr/ 86 Sr ratios of food items (caterpillars and snails), eggshells, and egg contents were indistinguishable within each site, but significantly different between the two sites. Mean 87 Sr/ 86 Sr ratios for the bones of adult females were significantly different between the two sites, but values were significantly lower than those of food items and eggshells at each site. Two of four adult individuals studied at each site had 87 Sr/ 86 Sr ratios lower than the entire range of values for local food sources. Mixing calculations indicate that up to 60% of skeletal strontium and calcium was derived from foods consumed in the winter grounds where lower 87 Sr/ 86 Sr ratios predominate. At each study site, the 87 Sr/ 86 Sr ratio of eggshells differed significantly between clutches, but the mean clutch 87 Sr/ 86 Sr ratios were unrelated to the skeletal 87 Sr/ 86 Sr ratio of the laying adult. These findings suggest that strontium (and hence calcium) for eggshell production in this species is derived predominantly from local food sources in breeding areas. Thus, reductions in available calcium in northern temperate ecosystems due to the influences of acid deposition could be potentially harmful to this and other species of migratory bird.

  20. Infrared Spectroscopy and Stable Isotope Geochemistry of Hydrous Silicate Glasses

    Energy Technology Data Exchange (ETDEWEB)

    Stolper, Edward

    2007-03-05

    The focus of this DOE-funded project has been the study of volatile components in magmas and the atmosphere. Over the twenty-one year period of this project, we have used experimental petrology and stable isotope geochemistry to study the behavior and properties of volatile components dissolved in silicate minerals and melts and glasses. More recently, we have also studied the concentration and isotopic composition of CO2 in the atmosphere, especially in relation to air quality issues in the Los Angeles basin.

  1. Geochemistry of the stable isotopes of silicon

    Energy Technology Data Exchange (ETDEWEB)

    Douthitt, C B [California Inst. of Tech., Pasadena (USA). Div. of Geological and Planetary Sciences

    1982-08-01

    One hundred thirty two new measurements of the relative abundances of the stable isotopes of silicon in terrestrial materials are presented. The total variation of delta/sup 30/Si found is 6.2 parts per thousand, centered on the mean of terrestrial mafic and ultramafic igneous rocks, delta/sup 30/Si = -0.4 parts per thousand. Igneous rocks show limited variation; coexisting minerals exhibit small, systematic silicon isotopic fractionations that are roughly 1/3 the magnitude of concomitant oxygen isotopic fractionations at 1150/sup 0/C. In both igneous minerals and rocks, delta/sup 30/Si shows a positive correlation with silicon content, as does delta/sup 18/O. Opal from both sponge spicules and sinters is light, with delta/sup 30/Si = -2.3 and -1.4 parts per thousand respectively. Large delta/sup 30/Si values of both positive and negative sign are reported for the first time from clay minerals, opaline phytoliths, and authigenic quartz. All highly fractionated samples were precipitated from solution at low temperatures; however, aqueous silicon is not measurably fractionated relative to quartz at equilibrium. A kinetic isotope fractionation of approximately 3.5 parts per thousand is postulated to occur during the low temperature precipitation of opal and, possibly, poorly ordered phyllosilicates, with the silicate phase being enriched in /sup 28/Si. This fractionation, coupled with a Rayleigh precipitation model, is capable of explaining most non-magmatic delta/sup 30/Si variations.

  2. Isotopic geochemistry of Fernando de Noronha

    International Nuclear Information System (INIS)

    Gerlach, D.C.; Stormer, J.C. Jr.; Mueller, P.A.

    1987-01-01

    Volcanic and hybabyssal rocks ranging in age from 12 to 3 Ma from the Fernando de Noronha archipelago in the western equatorial Atlantic Ocean can generally be devided into two age-compositional groups that have variable and distinct isotopic compositions. Predominantly older alkali basalts and trachytes are generally characterized by more radiogenic Sr-isotopic ( 87 Sr/ 86 Sr=0.70457-0.70485) compositions and less radiogenic Nd-isotopic ( 143 Nd/ 144 Nd=0.51271-0.51281) and Pb-isotopic ( 206 Pb/ 204 Pb=19.132-19.282) compositions relative to the generally younger, more alkaline Si-undersaturated rocks which include nephelinites, ankaratrites, and melilitites ( 87 Sr/ 86 Sr=0.70365-0.70418, 143 Nd/ 144 Nd=0.51277-0.51290, 206 Pb/ 204 Pb=19.317-19.565). These variations suggest the influence of at least two separate components in the source(s) of both series. One component is characterized by high Rb/Sr and low μ, possibly derived from delaminated subcontinental lithosphere, whereas the other has high μ and low Rb/Sr similar to the source of St. Helena lavas. A third component is suggested by correlated compositions in the latest alkaline, Si-undersaturated lavas, and this component may be derived from depleted mantle. These isotopic variations in conjunction with the generally increasing degree of alkalinity with time are consistent with the temporal depletion of a low-μ, high Rb/Sr component and increasing contributions from a high-μ component in the source of the volcanic rocks of Fernando de Noronha. (orig.)

  3. Stable isotope geochemistry : definitions, terminology, measurement and some applications

    International Nuclear Information System (INIS)

    Faure, K.

    2009-01-01

    In 1936, Alfred Nier produced the first precise measurement of isotope abundance ratios and his design still remains the basis of stable isotope mass spectrometry. With this gift from the physicists for routine measurement of isotope ratios, earth scientists began to explore the natural variations of isotopes. Thus began a new era in geoscience research with the hydrological cycle and marine palaeolimatic research being the first topics to be investigated. Stable isotope measurements have been applied to many fundamental problems in geochemistry, petrology, and paleoclimatology, as well as related fields in archaeology, anthropology, physical chemistry, biology and forensic sciences. These applications can be broadly classified into four main types: 1. Thermometry: Formation temperatures of rock and mineral systems are determined on the basis of temperature-dependent fractionations of the isotopic ratios between two or more cogenetic phases. 2. Tracers: Reservoirs like the ocean, the mantle, meteroic waters and organic matter have distinct stable isotope signatures that can be used to trace the origin of rocks, fluids, contaminants etc. 3. Reaction mechanism: Distinctions can be made between diffusion and recrystallization, open and closed systems and bacterial and thermogenic processes. 4. Chemostratigraphy: Abrupt changes (excursions) in the stable isotope ratios of ocean sediments and certain terrestrial materials can be used as stratigraphic markers. (author). 56 refs., 11 figs., 2 tabs.

  4. Stable isotope geochemistry : definitions, terminology, measurement and some applications

    International Nuclear Information System (INIS)

    Faure, K.

    2014-01-01

    In 1936, Alfred Nier produced the first precise measurement of isotope abundance ratios and his design still remains the basis of stable isotope mass spectrometry. With this gift from the physicists for routine measurement of isotope ratios, earth scientists began to explore the natural variations of isotopes. Thus began a new era in geoscience research with the hydrological cycle and marine palaeoclimatic research being the first topics to be investigated. Stable isotope measurements have been applied to many fundamental problems in geochemistry, petrology, and paleoclimatology, as well as related fields in archaeology, anthropology, physical chemistry, biology and forensic sciences. These applications can be broadly classified into four main types: 1. Thermometry: Formation temperatures of rock and mineral systems are determined on the basis of temperature-dependent fractionations of the isotopic ratios between two or more cogenetic phases. 2. Tracers: Reservoirs like the ocean, the mantle, meteoric waters and organic matter have distinct stable isotope signatures that can be used to trace the origin of rocks, fluids, contaminants etc. 3. Reaction mechanism: Distinctions can be made between diffusion and recrystallization, open and closed systems and bacterial and thermogenic processes. 4. Chemostratigraphy: Abrupt changes (excursions) in the stable isotope ratios of ocean sediments and certain terrestrial materials can be used as stratigraphic markers. (author)

  5. Stable isotope geochemistry: definitions, terminology, measurement and some applications

    International Nuclear Information System (INIS)

    Faure, K.

    2015-01-01

    In 1936, Alfred Nier produced the first precise measurement of isotope abundance ratios and his design still remains the basis of stable isotope mass spectrometry. With this gift from the physicists for routine measurement of isotope ratios, earth scientists began to explore the natural variations of isotopes. Thus began a new era in geoscience research with the hydrological cycle and marine palaeoclimatic research being the first topics to be investigated. Stable isotope measurements have been applied to many fundamental problems in geochemistry, petrology, and paleoclimatology, as well as related fields in archaeology, anthropology, physical chemistry, biology and forensic sciences. These applications can be broadly classified into four main types: 1. Thermometry: Formation temperatures of rock and mineral systems are determined on the basis of temperature-dependent fractionations of the isotopic ratios between two or more cogenetic phases. 2. Tracers: Reservoirs like the ocean, the mantle, meteoric waters and organic matter have distinct stable isotope signatures that can be used to trace the origin of rocks, fluids, contaminants etc. 3. Reaction mechanism: Distinctions can be made between diffusion and recrystallization, open and closed systems and bacterial and thermogenic processes. 4. Chemostratigraphy: Abrupt changes (excursions) in the stable isotope ratios of ocean sediments and certain terrestrial materials can be used as stratigraphic markers. (author).

  6. Stable isotope geochemistry : definitions, terminology, measurement and some applications

    International Nuclear Information System (INIS)

    Faure, K.

    2012-01-01

    In 1936, Alfred Nier produced the first precise measurement of isotope abundance ratios and his design still remains the basis of stable isotope mass spectrometry. With this gift from the physicists for routine measurement of isotope ratios, earth scientists began to explore the natural variations of isotopes. Thus began a new era in geoscience research with the hydrological cycle and marine palaeoclimatic research being the first topics to be investigated. Stable isotope measurements have been applied to many fundamental problems in geochemistry, petrology, and paleoclimatology, as well as related fields in archaeology, anthropology, physical chemistry, biology and forensic sciences. These applications can be broadly classified into four main types: 1. Thermometry: Formation temperatures of rock and mineral systems are determined on the basis of temperature-dependent fractionations of the isotopic ratios between two or more cogenetic phases. 2. Tracers: Reservoirs like the ocean, the mantle, meteoric waters and organic matter have distinct stable isotope signatures that can be used to trace the origin of rocks, fluids, contaminants etc. 3. Reaction mechanism: Distinctions can be made between diffusion and recrystallization, open and closed systems and bacterial and thermogenic processes. 4. Chemostratigraphy: Abrupt changes (excursions) in the stable isotope ratios of ocean sediments and certain terrestrial materials can be used as stratigraphic markers. (author). 89 refs., 12 figs., 2 tabs.

  7. Stable isotope geochemistry : definitions, terminology, measurement and some applications

    International Nuclear Information System (INIS)

    Faure, K.

    2008-01-01

    In 1936, Alfred Nier produced the first precise measurement of isotope abundance ratios and his design still remains the basis of stable isotope mass spectrometry. With this gift from the physicists for routine measurement of isotope ratios, earth scientists began to explore the natural variations of isotopes. Thus began a new era in geoscience research with the hydrological cycle and marine palaeolimatic research being the first topics to be investigated. Stable isotope measurements have been applied to many fundamental problems in geochemistry, petrology, and paleoclimatology, as well as related fields in archaeology, anthropology, physical chemistry, biology and forensic sciences. These applications can be broadly classified into four main types: 1. Thermometry: Formation temperatures of rock and mineral systems are determined on the basis of temperature-dependent fractionations of the isotopic ratios between two or more cogenetic phases. 2. Tracers: Reservoirs like the ocean, the mantle, meteroic waters and organic matter have distinct stable isotope signatures that can be used to trace the origin of rocks, fluids, contaminants etc. 3. Reaction mechanism: Distinctions can be made between diffusion and recrystallization, open and closed systems and bacterial and thermogenic processes. 4. Chemostratigraphy: Abrupt changes (excursions) in the stable isotope ratios of ocean sediments and certain terrestrial materials can be used as stratigraphic markers. (author). 56 refs., 11 figs., 2 tabs

  8. Stable isotope geochemistry : definitions, terminology, measurement and some applications

    International Nuclear Information System (INIS)

    Faure, K.

    2009-01-01

    In 1936, Alfred Nier produced the first precise measurement of isotope abundance ratios and his design still remains the basis of stable isotope mass spectrometry. With this gift from the physicists for routine measurement of isotope ratios, earth scientists began to explore the natural variations of isotopes. Thus began a new era in geoscience research with the hydrological cycle and marine palaeolimatic research being the first topics to be investigated. Stable isotope measurements have been applied to many fundamental problems in geochemistry, petrology, and paleoclimatology, as well as related fields in archaeology, anthropology, physical chemistry, biology and forensic sciences. These applications can be broadly classified into four main types: 1. Thermometry: Formation temperatures of rock and mineral systems are determined on the basis of temperature-dependent fractionations of the isotopic ratios between two or more cogenetic phases. 2. Tracers: Reservoirs like the ocean, the mantle, meteroic waters and organic matter have distinct stable isotope signatures that can be used to trace the origin of rocks, fluids, contaminants etc. 3. Reaction mechanism: Distinctions can be made between diffusion and recrystallization, open and closed systems and bacterial and thermogenic processes. 4. Chemostratigraphy: Abrupt changes (excursions) in the stable isotope ratios of ocean sediments and certain terrestrial materials can be used as stratigraphic markers. (author). 56 refs., 11 figs., 2 tabs

  9. Stable isotope geochemistry : definitions, terminology, measurement and some applications

    International Nuclear Information System (INIS)

    Faure, K.

    2016-01-01

    In 1936, Alfred Nier produced the first precise measurement of isotope abundance ratios and his design still remains the basis of stable isotope mass spectrometry. With this gift from the physicists for routine measurement of isotope ratios, earth scientists began to explore the natural variations of isotopes. Thus began a new era in geoscience research with the hydrological cycle and marine palaeoclimatic research being the first topics to be investigated. Stable isotope measurements have been applied to many fundamental problems in geochemistry, petrology, and paleoclimatology, as well as related fields in archaeology, anthropology, physical chemistry, biology and forensic sciences. These applications can be broadly classified into four main types: 1. Thermometry: Formation temperatures of rock and mineral systems are determined on the basis of temperature-dependent fractionations of the isotopic ratios between two or more cogenetic phases. 2. Tracers: Reservoirs like the ocean, the mantle, meteoric waters and organic matter have distinct stable isotope signatures that can be used to trace the origin of rocks, fluids, contaminants etc. 3. Reaction mechanism: Distinctions can be made between diffusion and recrystallization, open and closed systems and bacterial and thermogenic processes. 4. Chemostratigraphy: Abrupt changes (excursions) in the stable isotope ratios of ocean sediments and certain terrestrial materials can be used as stratigraphic markers. (author).

  10. Stable isotope geochemistry : definitions, terminology, measurement and some applications

    International Nuclear Information System (INIS)

    Faure, K.

    2013-01-01

    In 1936, Alfred Nier produced the first precise measurement of isotope abundance ratios and his design still remains the basis of stable isotope mass spectrometry. With this gift from the physicists for routine measurement of isotope ratios, earth scientists began to explore the natural variations of isotopes. Thus began a new era in geoscience research with the hydrological cycle and marine palaeoclimatic research being the first topics to be investigated. Stable isotope measurements have been applied to many fundamental problems in geochemistry, petrology, and paleoclimatology, as well as related fields in archaeology, anthropology, physical chemistry, biology and forensic sciences. These applications can be broadly classified into four main types: 1. Thermometry: Formation temperatures of rock and mineral systems are determined on the basis of temperature-dependent fractionations of the isotopic ratios between two or more cogenetic phases. 2. Tracers: Reservoirs like the ocean, the mantle, meteoric waters and organic matter have distinct stable isotope signatures that can be used to trace the origin of rocks, fluids, contaminants etc. 3. Reaction mechanism: Distinctions can be made between diffusion and recrystallization, open and closed systems and bacterial and thermogenic processes. 4. Chemostratigraphy: Abrupt changes (excursions) in the stable isotope ratios of ocean sediments and certain terrestrial materials can be used as stratigraphic markers. (author). 91 refs., 12 figs., 2 tabs.

  11. Isotope ratios of strontium and neodymium for characterizing earth mantle materials

    International Nuclear Information System (INIS)

    Brandt, S.B.; Lepin, V.S.; Maslovskaja, M.N.

    1985-01-01

    It is shown that the shares of mantle, crustal and sedimentary materials in rocks and ore deposits can be determined by isotope methods. Using Yakutian kimberlites as an example, mixing processes of mantle and crustal materials are illustrated with the aid of strontium isotopes. Due to the high sensitivity of strontium to hydrothermal effects, the combined use of neodymium and strontium isotopes is considered more appropriate to solve the problem of determining the share of mantle materials. This is demonstrated for rare earth minerals and alkaline rocks of Eastern Siberia and Mongolia. (author)

  12. STABLE ISOTOPE GEOCHEMISTRY OF MASSIVE ICE

    Directory of Open Access Journals (Sweden)

    Yurij K. Vasil’chuk

    2016-01-01

    Full Text Available The paper summarises stable-isotope research on massive ice in the Russian and North American Arctic, and includes the latest understanding of massive-ice formation. A new classification of massive-ice complexes is proposed, encompassing the range and variabilityof massive ice. It distinguishes two new categories of massive-ice complexes: homogeneousmassive-ice complexes have a similar structure, properties and genesis throughout, whereasheterogeneous massive-ice complexes vary spatially (in their structure and properties andgenetically within a locality and consist of two or more homogeneous massive-ice bodies.Analysis of pollen and spores in massive ice from Subarctic regions and from ice and snow cover of Arctic ice caps assists with interpretation of the origin of massive ice. Radiocarbon ages of massive ice and host sediments are considered together with isotope values of heavy oxygen and deuterium from massive ice plotted at a uniform scale in order to assist interpretation and correlation of the ice.

  13. Stable isotope geochemistry of deep sea cherts

    Energy Technology Data Exchange (ETDEWEB)

    Kolodny, Y; Epstein, S [California Inst. of Tech., Pasadena (USA). Div. of Geological Sciences

    1976-10-01

    Seventy four samples of DSDP (Deep Sea Drilling Project) recovered cherts of Jurassic to Miocene age from varying locations, and 27 samples of on-land exposed cherts were analyzed for the isotopic composition of their oxygen and hydrogen. These studies were accompanied by mineralogical analyses and some isotopic analyses of the coexisting carbonates. delta/sup 18/0 of chert ranges between 27 and 39 parts per thousand relative to SMOW, delta/sup 18/0 of porcellanite - between 30 and 42 parts per thousand. The consistent enrichment of opal-CT in porcellanites in /sup 18/0 with respect to coexisting microcrystalline quartz in chert is probably a reflection of a different temperature (depth) of diagenesis of the two phases. delta/sup 18/0 of deep sea cherts generally decrease with increasing age, indicating an overall cooling of the ocean bottom during the last 150 m.y. A comparison of this trend with that recorded by benthonic foraminifera (Douglas et al., Initial Reports of the Deep Sea Drilling Project; 32:509(1975)) indicates the possibility of delta/sup 18/0 in deep sea cherts not being frozen in until several tens of millions of years after deposition. Cherts of any Age show a spread of delta/sup 18/0 values, increasing diagenesis being reflected in a lowering of delta/sup 18/0. Drusy quartz has the lowest delta/sup 18/0 values. On land exposed cherts are consistently depleted in /sup 18/0 in comparison to their deep sea time equivalent cherts. Water extracted from deep sea cherts ranges between 0.5 and 1.4 wt%. deltaD of this water ranges between -78 and -95 parts per thousand and is not a function of delta/sup 18/0 of the cherts (or the temperature of their formation).

  14. Early African Diaspora in colonial Campeche, Mexico: strontium isotopic evidence.

    Science.gov (United States)

    Price, T Douglas; Tiesler, Vera; Burton, James H

    2006-08-01

    Construction activities around Campeche's central park led to the discovery of an early colonial church and an associated burial ground, in use from the mid-16th century AD to the late 17th century. Remains of some individuals revealed dental mutilations characteristic of West Africa. Analyses of strontium isotopes of dental enamel from these individuals yielded unusually high (87)Sr/(86)Sr ratios, inconsistent with an origin in Mesoamerica, but consistent with an origin in West Africa in terrain underlain by the West Africa Craton, perhaps near the port of Elmina, a principal source of slaves for the New World during the 16th century. These individuals likely represent some of the earliest representatives of the African Diaspora in the Americas.

  15. Strontium isotopes in carbonate deposits at Crater Flat, Nevada

    International Nuclear Information System (INIS)

    Marshall, B.D.; Futa, K.; Peterman, Z.E.; Stuckless, J.S.

    1991-01-01

    Strontium isotope studies of carbonates from soils, veins, eolian dust and Paleozoic basement sampled near Crater Flat, southwest of Yucca Mountain, provide evidence for the origins of these materials. Vein and soil carbonates have nearly identical ranges of 87 Sr/ 86 Sr, and eolian material has 87 Sr/ 86 Sr ratios at the lower end of the pedogenic range. The average 87 Sr/ 86 Sr of Paleozoic basement from Black Marble Hill is similar to the 87 Sr/ 86 Sr in the eolian dust, perhaps indicating a local source for this material. Possible spring deposits have generally higher 87 Sr/ 86 Sr than the other carbonates. These data are compared with similar data from areas east of Yucca Mountain

  16. Strontium isotopes in carbonate deposits at Crater Flat, Nevada

    International Nuclear Information System (INIS)

    Marshall, B.D.; Futa, K.; Peterman, Z.E.; Stuckless, J.S.

    1991-01-01

    Strontium isotope studies of carbonates from soils, veins, eolian dust and Paleozoic basement samples near Crater Flat, southwest of Yucca Mountain, provide evidence for the origins of these materials. Vein and soil carbonates have nearly identical ranges of 87 Sr/ 86 Sr ratios at the lower end of the pedogenic range. The average 87 Sr/ 86 Sr of Paleozoic basement from Black Marble Hill is similar to the 87 Sr/ 86 Sr in the eolian dust, perhaps indicating a local source for this material. Possible spring deposits have generally higher 87 Sr/ 86 Sr than the other carbonates. These data are compared with similar data from areas east of Yucca Mountain. 7 refs., 5 figs

  17. Strontium isotope fractionation in soils and pedogenic processes

    Energy Technology Data Exchange (ETDEWEB)

    Shalev, Netta [Institute of Earth Sciences, The Hebrew University of Jerusalem, 91904 Jerusalem (Israel); Geological Survey of Israel, 30 Malkhe Israel Street, 95501 Jerusalem (Israel); Lazar, Boaz [Institute of Earth Sciences, The Hebrew University of Jerusalem, 91904 Jerusalem (Israel); Halicz, Ludwik; Stein, Mordechai; Gavrieli, Ittai; Sandler, Amir; Segal, Irena [Geological Survey of Israel, 30 Malkhe Israel Street, 95501 Jerusalem (Israel)

    2013-07-01

    The stable isotope composition of strontium (the ratio {sup 88}Sr/{sup 86}Sr expressed as δ{sup 88/86}Sr) showed significant fractionation in mountain soils of the Judea Highland. In order to understand this phenomenon, we studied the elemental composition and the stable and radiogenic Sr isotopic composition in soil transects conducted from semi-arid (desert fringe) to wetter (Mediterranean) climate zones. These transects were selected because the degree of soil leaching depends on the amount of precipitation and the permeability of the underlying bedrock. These soils are the pedogenic products of leaching of the accumulated desert dust and the underlying carbonate bed-rocks resulting in, among others, enrichment of the residual soils in Al-clays. A clear negative correlation was found between the δ{sup 88/86}Sr and Al{sub 2}O{sub 3} (Al-clay content) values of the soils, the high δ{sup 88/86}Sr-low Al{sub 2}O{sub 3} being the dust end-member. This preliminary study demonstrates the feasibility of using stable {sup 88}Sr-{sup 86}Sr isotopes as tracers of terrestrial weathering processes. (authors)

  18. Sea water strontium isotopes, acid rain, and the cretaceous-tertiary boundary

    International Nuclear Information System (INIS)

    MacDougall, J.D.

    1988-01-01

    A large bolide impact at the end of the Cretaceous would have produced significant amounts of nitrogen oxides by shock heating of the atmosphere. The resulting acid precipitation would have increased continental weathering greatly and could be an explanation for the observed high ratio of strontium-87 to strontium-86 in sea water at about this time, due to the dissolution of large amounts of strontium from the continental crust. Spikes to high values in the sea water strontium isotope record at other times may reflect similar episodes. 17 references, 1 figure, 1 table

  19. Seawater strontium isotopes, acid rain, and the Cretaceous-Tertiary boundary

    Science.gov (United States)

    Macdougall, J. D.

    1988-01-01

    A large bolide impact at the end of the Cretaceous would have produced significant amounts of nitrogen oxides by shock heating of the atmosphere. The resulting acid precipitation would have increased continental weathering greatly and could be an explanation for the observed high ratio of strontium-87 to strontium-86 in seawater at about this time, due to the dissolution of large amounts of strontium from the continental crust. Spikes to high values in the seawater strontium isotope record at other times may reflect similar episodes.

  20. Strontium isotope model of formation of Blatna granodiorite

    International Nuclear Information System (INIS)

    Bendl, J.; Vokurka, K.

    1989-01-01

    The Blatna granodiorite is the second most abundant rock type of the Central Bohemian pluton. It belongs to the tonalite group. The Rb-Sr isochrone was constructed from granodiorite and mixed aplopegmatite-granodiorite whole rock samples. The age of final Sr isotopic homogenisation was found to be 331±9 Ma and the initial ratio of 87 Sr/ 86 Sr 0.7072±0.0015. The solidification temperature of the granodiorite (Whitney -Stormer, 1977) is 550±50 degC and that of the aplopegmatite 460±50 degC. The average Sr concentration in granodiorite is 331 ppm, that of Rb is 186 ppm. Values of 170 and 14 were found for the ratios K/Rb and Srx10 3 /Ca, respectively. REE patterns reveal a crustal component overprint. Mass balance calculations based on Sr isotopes, its concentration and on the overall geochemistry of the pluton and of the Moldanubian rock show that magma might have been generated as a mixture of about 30-50% of mantle and of 50-70% of upper crust materials. A certain part of the mantle component was brought to the region in the form of volcanics. The precursors of the crustal component might have been represented by recycled previous volcanosedimentary material with complex crustal history. (author). 4 figs., 2 tabs., 13 refs

  1. Stable and strontium isotopic records of molluscan shells, lower jurassic, Cuenca Neuquina, southwestern Mendoza, Argentina

    International Nuclear Information System (INIS)

    Cagnoni, M.C.; Valencio, S.A.; Ramos, A.M; Riccardi, A.C; Panarello, H.O

    2001-01-01

    The strontium, carbon and oxygen isotopic signal of the past oceans is accurately recorded by authigenic marine minerals such as carbonates, sulfates and phosphates. The variation of these isotope ratios through the geological time is used as a tool in correlating and dating marine sedimentary rocks. Many works have been done concerning to the changes in carbon, oxygen and strontium isotope ratios of different marine successions in the world. These allow the construction of curves of secular variations of the isotope signals with geological time (Jones et al., 1994a, 1994b; Veizer et al., 1999; Jacobsen and Kaufman, 1999). This work presents strontium, carbon and oxygen isotope ratios of Early Jurassic biogenic marine carbonates of Cuenca Neuquina in southwestern Mendoza (au)

  2. Hydrologic inferences from strontium isotopes in pore water from the unsaturated zone at Yucca Mountain, Nevada

    International Nuclear Information System (INIS)

    Marshall, B.D.; Futa, K.; Peterman, Z.E.

    1997-01-01

    Calcite is ubiquitous at Yucca Mountain, occurring in the soils and as fracture and cavity coatings within the volcanic tuff section. Strontium is a trace element in calcite, generally at the tens to hundreds of ppm level. Because calcite contains very little rubidium and the half-life of the 87 Rb parent is billions of years, the 87 Sr/ 86 Sr ratios of the calcite record the ratio in the water from which the calcite precipitated. Dissolution and reprecipitation does not alter these compositions so that, in the absence of other sources of strontium, one would expect the strontium ratios along a flow path to preserve variations inherited from strontium in the soil zone. Strontium isotope compositions of calcites from various settings in the Yucca Mountain region have contributed to the understanding of the unsaturated zone (UZ), especially in distinguishing unsaturated zone calcite from saturated zone calcite. Different populations of calcite have been compared, either to group them together or distinguish them from each other in terms of their strontium isotope compositions. Ground water and perched water have also been analyzed; this paper presents strontium isotope data obtained on pore water

  3. Calcium Isotope Geochemistry: Research Horizons and Nanoscale Fractionation Processes

    Science.gov (United States)

    Watkins, J. M.; Depaolo, D. J.; Richter, F. M.; Fantle, M. S.; Simon, J. I.; Ryerson, F. J.; Ewing, S. A.; Turchyn, A. V.; Yang, W.; Owens, T. L.

    2008-12-01

    Interest in studies of calcium isotope variations in nature continues to increase. Investigations span human biology, plants and soils, oceanography and paleoclimate, early solar system processes, aqueous geochemistry, and silicate liquid structure. Variations in the 44Ca/40Ca ratio are generally small, about 5 ‰, but gradual small improvements in analytical capability now yield 0.05 to 0.1 ‰ resolution. The field is still plagued by a lack of universal standards for isotope ratios and data representation, but these are secondary issues. Traditional isotopic systems have been based in equilibrium thermodynamics, which can explain the magnitude and sign of observed mass-dependent fractionation behavior. For Ca isotopes this is not the case. There is still no reliable way to estimate the equilibrium free energy associated with isotopic exchange between most phases of interest. Experiments are difficult to interpret because it is almost impossible to precipitate minerals from aqueous solution at equilibrium at low temperature. Some studies suggest that, for example, there is no equilibrium isotopic fractionation between calcite and dissolved aqueous Ca. There is good evidence that most Ca isotopic fractionation is caused by kinetic effects. The details of the controlling processes are still missing, and without this mechanistic understanding it is difficult to fully understand the implications of natural isotopic variations. Recent work on dissolved Ca, calcite, and sulfates in both laboratory and natural settings is shedding light on where the fractionation may arise. There is emerging evidence for mass dependent fractionation associated with aqueous diffusion, but probably the primary source of the effects is in the details of precipitation of minerals from solution. This makes the fractionation potentially dependent on a number of factors, including solution composition and mineral growth rate. The next challenge is to develop appropriate experimental tests and

  4. Strontium isotopic study of sediment from the Ross Sea

    International Nuclear Information System (INIS)

    Kovach, J.; Faure, G.

    1977-01-01

    A preliminary report summarizing the results of a study of the strontium-87/strontium-86 ratios and of the rubidium and strontium concentrations of the fine-grained (less than 150 microns) noncarbonate fractions of sediment samples from core E32-25 raised from a depth of 327 fathoms in the Ross Sea at 78 0 31.0'S 164 0 24.7'W was presented. The strontium-87/strontium-86 ratios of the samples analyzed range from 0.7119 to 0.7220. Rubidium and strontium concentrations range, respectively, from 126 to 164 parts per million and from 113 to 174 parts per million. The observed strontium-87/strontium-86 ratios and strontium concentrations in sediment samples from core E32-25 fit a hyperbolic curve. These ratios can be used to estimate the concentrations of volcanogenic detritus in the sediment samples. The results of this study provide additional baseline data for anticipated future studies of sediment cores to be recovered from beneath the Ross Ice Shelf by the Ross Ice Shelf Project. 1 figure

  5. Sr isotope geochemistry of East Alpine mineral deposits and mass spectrometric analyses of fluid inclusions

    International Nuclear Information System (INIS)

    Grum, W.

    1995-05-01

    Strontium isotope geochemistry and deformational history of selected carbonate-hosted deposits from different tectonic positions in the Eastern Alps were studied. In this context an equipment has been constructed to analyze the composition of volatile components of fluid inclusions (FI). Based on the results of Sr-isotopic investigations two groups of deposits are discriminated: Deposits formed by formation waters and/or metamorphogenic fluids: Tux (magnesite, scheelite), Otterzug (barite), Lassing (magnesite), Rabenwald (talc), Laussa and Mooseck (fluorite). The mineralizing fluids are derived from different sedimentary rock series and therefore 87 Sr/ 86 Sr-ratios vary between 0.707 and 0.719. Deposits situated along fault zones: Lassing (talc), Gasteiner Tal (Silberpfennig area; gold), Schlaining (stibnite) and Waldenstein (specularite). Sr isotope ratios of the mineralizing fluids from Lassing, Waldenstein and Schlaining ranges from 0.7112 to 0.7127 and are therefore thought to have scavenged the East Alpine crystalline. The mineralizing solutions of the Gasteiner Tal deposit may either have equilibrated with low radiogenic sedimentary or with (ultra-)basic rocks. A cracking chamber has been constructed in order to open FI by cracking for mass spectrometric analysis of volatile components. Gases are analysed using a quadrupole mass spectrometer. The desorption of gas from metal and sample surfaces during cracking can be neglected. The amount of gas released from the mineral lattices was studied. With that fast method ore bearing from barren host rocks have been distinguished by different composition of the FI at the Brixlegg barite mineralization (Eastern Alps). Within the Galway fluorite deposit (Ireland) different fluids were involved and mass spectrometric analysis were carried out to characterize these different fluids and to identify their origin. (author)

  6. V Congress of Spanish Geochemistry

    International Nuclear Information System (INIS)

    1993-01-01

    This proceedings book present the lectures of V Spanish geochemistry Congress. The sessions were: 1.- Materials geochemistry and geologic process. 2.- Geochemistry prospection 3.- Environmental geochemistry 4.- Isotopic geochemistry 5.- Organic geochemistry 6.- Natural materials geochemistry for industry 7.- Hydrogeochemistry 8.- Mathematical models in geochemistry 9.- Analysis methods in geochemistry 10.-Training of geochemistry 11.-Cosmochemistry

  7. SPATIAL Short Courses Build Expertise and Community in Isotope Geochemistry

    Science.gov (United States)

    Riggs, E. M.; Bowen, G. J.

    2015-12-01

    The SPATIAL short course at the University of Utah is designed for graduate students and professionals in the earth and environmental sciences from around the globe. An integral part of the broader, NSF-funded Inter-university Training for Continental-scale Ecology (ITCE) project, the course is an intensive two-week field, classroom and laboratory experience with internationally-known researchers as instructors. The course focuses on stable isotope geochemistry coupled with spatial analysis techniques. Participants do not typically know each other or this research community well upon entering. One of the stated goals of the overall project is to build a community of practice around these techniques. This design is common in many professional fields, but is not often applied at the graduate level nor formally assessed in the earth sciences. Paired pre- and post-tests were administered before the start and after the close of the short courses over 3 years. The survey is a set of instruments adapted from social-cognitive psychology measuring changes in identity and community with other items to measure content knowledge outcomes. We see a subtle, consistent convergence of identities between large-scale isotope geochemistry and participants' research areas. Results also show that the course generates an increase in understanding about stable isotopes' use and application. The data show the SPATIAL course is very effective at bringing students together socially with each other and with faculty to create an environment that fosters community and scientific cooperation. Semi-structured pre-and post- interviews were conducted to understand the program elements that generated gains in learning and community. Participants were selected based on initial responses on the pre-survey to capture the range of initial conditions for the group. Qualitative analysis shows that the major factors for participants were 1) ready access to researchers in an informal setting during the

  8. Strontium isotopes as an indicator for groundwater salinity sources in the Kirkuk region, Iraq

    Energy Technology Data Exchange (ETDEWEB)

    Sahib, Layth Y. [Institute for Applied Geosciences, Technische Universität Darmstadt, Schnittspahnstraße 9, 64287 Darmstadt (Germany); Geology Department, College of Science, University of Baghdad, Jadreya, Baghdad (Iraq); Marandi, Andres; Schüth, Christoph [Institute for Applied Geosciences, Technische Universität Darmstadt, Schnittspahnstraße 9, 64287 Darmstadt (Germany)

    2016-08-15

    The Kirkuk region in northern Iraq hosts some of the largest oil fields in the Middle East. Several anticline structures enabled vertical migration and entrapment of the oil. Frequently, complex fracture systems and faults cut across the Eocene and middle Oligocene reservoirs and the cap rock, the Fatha Formation of Miocene age. Seepage of crude oil and oil field brines are therefore a common observation in the anticline axes and contamination of shallow groundwater resources is a major concern. In this study, 65 water samples were collected in the Kirkuk region to analyze and distinguish mixing processes between shallow groundwater resources, uprising oil field brines, and dissolution of gypsum and halite from the Fatha Formation. Hydrochemical analyses of the water samples included general hydrochemistry, stable water isotopes, as well as strontium concentrations and for 22 of the samples strontium isotopes ({sup 87}Sr/{sup 86}Sr). Strontium concentrations increased close to the anticline axes with highest concentrations in the oil field brines (300 mg/l). Strontium isotopes proved to be a valuable tool to distinguish mixing processes as isotope signatures of the oil field brines and of waters from the Fatha Formation are significantly different. It could be shown, that mixing of shallow groundwater with oil field brines is occurring close to the major fault zones in the anticlines but high concentrations of strontium in the water samples are mainly due to dissolution from the Fatha Formation. - Highlights: • This field study evaluates the salinity sources in the groundwater in Kirkuk region. • Salinity is related to evaporates dissolving and/or mixing with oil field brine. • Strontium isotopes proved to be a valuable tool to distinguish mixing processes.

  9. Growth of the continental crust: constraints from radiogenic isotope geochemistry

    International Nuclear Information System (INIS)

    Taylor, P.N.

    1988-01-01

    Most models for evolution of continental crust are expressed in the form of a diagram illustrating the cumulative crustal mass (normalized relative to the present crustal mass) as a function of time. Thus, geochronological data inevitably play a major role in either constructing or testing crustal growth models. For all models, determining the start-time for effective crustal accretion is of vital importance. To this end, the continuing search for, and reliable characterization of, the most ancient crustal rock-units remains a worthy enterprise. Another important role for geochronology and radiogenic isotope geochemistry is to assess the status of major geological events as period either of new crust generation or of reworking of earlier formed continental crust. For age characterization of major geological provinces, using the critieria outined, the mass (or volume) of crust surviving to the present day should be determinable as a function of crust formation age. More recent developments, however, appear to set severe limitations on recycling of crust, at least by the process of sediment subduction. In modeling crustal growth without recycling, valuable constaints on growth rate variations through time can be provided if variations in the average age of the continental crust can be monitored through geological history. The question of the average age of the exposed continental crust was addressed by determining Sm-Nd crustal residence model ages (T-CR) for fine-grained sediment loads of many of the world's major rivers

  10. Determination of strontium and lead isotope ratios of grains using high resolution inductively coupled plasma mass spectrometer with single collector

    International Nuclear Information System (INIS)

    Shinozaki, Miyuki; Ariyama, Kaoru; Kawasaki, Akira; Hirata, Takafumi

    2010-01-01

    A method for determining strontium and lead isotope ratios of grains was developed. The samples investigated in this study were rice, barley and wheat. The samples were digested with nitric acid and hydrogen peroxide, and heated in a heating block. Strontium and lead were separated from the matrix by adding an acid digested solution into a column packed with Sr resin, which has selectivity for the absorption of strontium and lead. Strontium and lead isotope ratios were determined using a high-resolution inductively coupled plasma mass spectrometer (HR-ICP-MS) with a single collector. The intraday relative standard deviations of 87 Sr/ 86 Sr and lead isotope ratios ( 204 Pb/ 206 Pb, 207 Pb/ 206 Pb, 208 Pb/ 206 Pb) by HR-ICP-MS measurements were < 0.06% and around 0.1%, respectively. This method enabled us to determine strontium and lead isotope ratios in two days. (author)

  11. The determination of initial ratio of strontium isotope in rocks and its geological application

    International Nuclear Information System (INIS)

    Ying Junlong; Zhao Puyun; Lin Xiulan

    1989-04-01

    The method to determine the initial ratio of strontium isotopes existed in rocks of poor rubidium and rich strontium and main carrier minerals is introduced. The initial ratio obtained from this method is equivalent to that acquired by Rb-Sr isochrone. Based on this result, information on regional rock genesis and mineralization regularities can be provided. It has great significance in the research on activities of ancient continental margin and material sources as well as their evolution. The migration of rock, and ore-forming materials, matallogenetic mechanism and its distribution in the space and time evolution are studied by using these data. In conclusion, the determination of strontium isotopes has broad prospects in the geological research

  12. Rubidium-strontium and uranium-lead isotopic age studies

    International Nuclear Information System (INIS)

    Loveridge, W.D.

    1980-01-01

    Rubidium-strontium whole rock isochron ages and initial 87 Sr/ 86 Sr ratios and uranium-lead ages on zircon from suites of samples selected from localities across Canada are presented. Descriptions of the geological probelms and interpretations of the measured ages are included. Laboratory age determination methods and techniques are described or referenced. (auth)

  13. The strontium isotopic composition of seawater, and seawater-oceanic crust interaction

    International Nuclear Information System (INIS)

    Spooner, E.T.C.

    1976-01-01

    The 87 Sr/ 86 Sr ratio of seawater strontium (0.7091) is less than the 87 Sr/ 86 Sr ratio of dissolved strontium delivered to the oceans by continental run-off (approximately 0.716). Isotope exchange with strontium isotopically lighter oceanic crust during hydrothermal convection within spreading oceanic ridges can explain this observation. In quantitative terms, the current 87 Sr/ 86 Sr ratio of seawater (0.7091) may be maintained by balancing the continental run-off flux of strontium (0.59 x 10 12 g/yr) against a hydrothermal recirculation flux of 3.6 x 10 12 g/yr, during which the 87 Sr/ 86 Sr ratio of seawater drops by 0.0011. A concomitant mean increase in the 87 Sr/ 86 Sr ratio of the upper 4.5 km of oceanic crust of 0.0010 (0.7029-0.7039) should be produced. This required 87 Sr enrichment has been observed in hydrothermally metamorphosed ophiolitic rocks from the Troodos Massif, Cyprus. The post-Upper Cretaceous increase in the strontium isotopic composition of seawater (approximately 0.7075-0.7091) covaries smoothly with inferred increase in land area. This suggests that during this period the main factor which has caused variability in the 87 Sr/ 86 Sr ratio of seawater strontium could have been variation in the magnitude of the continental run-off flux caused by variation in land area. Variations in land area may themselves have been partly a consequence of variations in global mean sea-floor spreading rate. (Auth.)

  14. Strontium isotopes and the reconstruction of the Chaco regional system: evaluating uncertainty with Bayesian mixing models.

    Directory of Open Access Journals (Sweden)

    Brandon Lee Drake

    Full Text Available Strontium isotope sourcing has become a common and useful method for assigning sources to archaeological artifacts.In Chaco Canyon, an Ancestral Pueblo regional center in New Mexico, previous studiesusing these methods have suggested that significant portion of maize and wood originate in the Chuska Mountains region, 75 km to the West [corrected]. In the present manuscript, these results were tested using both frequentist methods (to determine if geochemical sources can truly be differentiated and Bayesian methods (to address uncertainty in geochemical source attribution. It was found that Chaco Canyon and the Chuska Mountain region are not easily distinguishable based on radiogenic strontium isotope values. The strontium profiles of many geochemical sources in the region overlap, making it difficult to definitively identify any one particular geochemical source for the canyon's pre-historic maize. Bayesian mixing models support the argument that some spruce and fir wood originated in the San Mateo Mountains, but that this cannot explain all 87Sr/86Sr values in Chaco timber. Overall radiogenic strontium isotope data do not clearly identify a single major geochemical source for maize, ponderosa, and most spruce/fir timber. As such, the degree to which Chaco Canyon relied upon outside support for both food and construction material is still ambiguous.

  15. Determining flow, recharge, and vadose zone drainage in an unconfined aquifer from groundwater strontium isotope measurements, Pasco Basin, WA

    International Nuclear Information System (INIS)

    2004-01-01

    Strontium isotope compositions (87Sr/86Sr) measured in groundwater samples from 273 wells in the Pasco Basin unconfined aquifer below the Hanford Site show large and systematic variations that provide constraints on groundwater recharge, weathering rates of the aquifer host rocks, communication between unconfined and deeper confined aquifers, and vadose zone-groundwater interaction. The impact of millions of cubic meters of wastewater discharged to the vadose zone (103-105 times higher than ambient drainage) shows up strikingly on maps of groundwater 87Sr/86Sr. Extensive access through the many groundwater monitoring wells at the site allows for an unprecedented opportunity to evaluate the strontium geochemistry of a major aquifer, hosted primarily in unconsolidated sediments, and relate it to both long term properties and recent disturbances. Groundwater 87Sr/86Sr increases systematically from 0.707 to 0.712 from west to east across the Hanford Site, in the general direction of groundwater flow, as a result of addition of Sr from the weathering of aquifer sediments and from diffuse drainage through the vadose zone. The lower 87Sr/86Sr groundwater reflects recharge waters that have acquired Sr from Columbia River Basalts. Based on a steady-state model of Sr reactive transport and drainage, there is an average natural drainage flux of 0-1.4 mm/yr near the western margin of the Hanford Site, and ambient drainage may be up to 30 mm/yr in the center of the site assuming an average bulk rock weathering rate of 10-7.5 g/g/yr

  16. Verification of strontium isotopes and its possible source in Indian basmati rice for geographical authentication study

    International Nuclear Information System (INIS)

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

    2015-01-01

    Due to globalization of food and agriculture product's market, there is increasing awareness of safety and authenticity of the food products. Consumers continuously demand the reassurance of origin and content of their foods. Hence safety and authenticity of food has been a growing analytical challenge. Basmati rice, the unique aromatic quality rice and a nature's gift to Indian sub-continent is produced and consumed on a large scale. Due to its profitable market as well as great demand overseas true Basmati rice market is facing unfair competition by unscrupulous producers for profit. Very few researches for geographical authentication are available for Indian basmati rice. Sr isotope composition of rice could be used as a geographical source indicator; however, little information is available on the possible source (lithogenic, biogenic, silicate, carbonate) of Sr in Rice or any other food stuff for tracing the geographical origin using Strontium isotopes as tracer. Hence in order to determine suitability of strontium isotopes as tracer and its possible source in rice for geographical authentication study, strontium isotope signature study of authentic Indian Basmati rice along with in situ soil and water of that region have been carried out

  17. Proceedings of 1. international symposium on applied isotope geochemistry (AIG-1)

    International Nuclear Information System (INIS)

    Aaberg, G.; Joergensen, E.B.

    1993-09-01

    The publication is a compilation of abstracts from the ''1. international symposium on applied isotope geochemistry (AIG-1)'' in Norway. The symposium was the first of its kind taking up different applications of most of the available isotopic systems and thus covered a wide range of topics from: 1) Water resources, hydrology, geomedicine and environmental problems, 2) Petroleum exploration and production, 3) Mineral exploration and 4) Analytical methods

  18. Geochemical and strontium isotope characterization of produced waters from Marcellus Shale natural gas extraction.

    Science.gov (United States)

    Chapman, Elizabeth C; Capo, Rosemary C; Stewart, Brian W; Kirby, Carl S; Hammack, Richard W; Schroeder, Karl T; Edenborn, Harry M

    2012-03-20

    Extraction of natural gas by hydraulic fracturing of the Middle Devonian Marcellus Shale, a major gas-bearing unit in the Appalachian Basin, results in significant quantities of produced water containing high total dissolved solids (TDS). We carried out a strontium (Sr) isotope investigation to determine the utility of Sr isotopes in identifying and quantifying the interaction of Marcellus Formation produced waters with other waters in the Appalachian Basin in the event of an accidental release, and to provide information about the source of the dissolved solids. Strontium isotopic ratios of Marcellus produced waters collected over a geographic range of ~375 km from southwestern to northeastern Pennsylvania define a relatively narrow set of values (ε(Sr)(SW) = +13.8 to +41.6, where ε(Sr) (SW) is the deviation of the (87)Sr/(86)Sr ratio from that of seawater in parts per 10(4)); this isotopic range falls above that of Middle Devonian seawater, and is distinct from most western Pennsylvania acid mine drainage and Upper Devonian Venango Group oil and gas brines. The uniformity of the isotope ratios suggests a basin-wide source of dissolved solids with a component that is more radiogenic than seawater. Mixing models indicate that Sr isotope ratios can be used to sensitively differentiate between Marcellus Formation produced water and other potential sources of TDS into ground or surface waters.

  19. Generator coordinate method for triaxial quadrupole collective dynamics in strontium isotopes

    International Nuclear Information System (INIS)

    Bonche, P.; Dobaczewski, J.; Flocard, H.; Heenen, P.H.

    1991-01-01

    We discuss the algebraic structure of the generator coordinate method for triaxial quadrupole collective motion. The collective solutions are classified according to the representations of the permutation group of the intrinsic axes. Our method amounts to an approximate angular momentum projection. We apply it to a study of the spherical to deformed shape transition in light even strontium isotopes 78-88 Sr. We find that triaxial configurations play a significant role in explaining the structure of the transitional isotopes 80-82 Sr

  20. Reduced population variance in strontium isotope values informs domesticated turkey use at Chaco Canyon, New Mexico, USA

    Science.gov (United States)

    Grimstead, Deanna N; Reynolds, Amanda C; Hudson, Adam M; Akins, Nancy J; Betancourt, Julio L.

    2016-01-01

    Traditionally strontium isotopes (87Sr/86Sr) have been used as a sourcing tool in numerous archaeological artifact classes. The research presented here demonstrates that 87Sr/86Srbioapatite ratios also can be used at a population level to investigate the presence of domesticated animals and methods of management. The proposed methodology combines ecology, isotope geochemistry, and behavioral ecology to assess the presence and nature of turkey (Meleagris gallopavo) domestication. This case study utilizes 87Sr/86Srbioapatite ratios from teeth and bones of archaeological turkey, deer (Odocoileus sp.), lagomorph (Lepus sp. and Sylvilagus sp.), and prairie-dog (Cynomys sp.) from Chaco Canyon, New Mexico, U.S.A. (ca. A.D. 800 – 1250). Wild deer and turkey from the southwestern U.S.A. have much larger home ranges and dispersal behaviors (measured in kilometers) when compared to lagomorphs and prairie dogs (measured in meters). Hunted deer and wild turkey from archaeological contexts at Chaco Canyon are expected to have a higher variance in their 87Sr/86Srbioapatite ratios, when compared to small range taxa (lagomorphs and prairie dogs). Contrary to this expectation, 87Sr/86Srbioapatite values of turkey bones from Chacoan assemblages have a much lower variance than deer and are similar to that of smaller mammals. The sampled turkey values show variability most similar to lagomorphs and prairie dogs, suggesting the turkeys from Chaco Canyon were consuming a uniform diet and/or were constrained within a limited home range, indicating at least proto-domestication. The population approach has wide applicability for evaluating the presence and nature of domestication when combined with paleoecology and behavioral ecology in a variety of animals and environments.

  1. Laser spectroscopy of radioactive barium and strontium isotopes

    International Nuclear Information System (INIS)

    Martin, A.G.

    1986-01-01

    An atomic beam system and a high resolution computer controlled dye laser system were developed to perform isotope shift measurements on accelerator-produced radioactive isotopes. Two different techniques were used to transport the radioactive isotopes to the laser interaction region. The first technique was based on the thermalization and deionization of the nuclear reaction products in a helium buffer gas. The reaction products were subsequently transported in the gas to the laser beam along a capillary tube. This technique suffered from problems with chemical reactions between impurities in the buffer gas and the reaction products and proved to be unsuccessful. The second technique was based on the implantation of the reaction products into a metal lattice. Subsequent heating of the metal lattice released the implanted ions from which an atomic beam was formed. The photon burst technique was used to enable detection of the extremely weak atomic beams formed in this manner. Measurements were performed of the known isotope shifts of radioactive 128 Ba and 126 Ba to test the sensitivity of the system. The previously unmeasured isotope shift of radioactive 82 Sr also was determined, and the result obtained was compared to predictions using the droplet model

  2. Petrogenesis of Miocene alkaline volcanic suites from western Bohemia. Whole rock geochemistry and Sr-Nd-Pb isotopic signatures.

    Czech Academy of Sciences Publication Activity Database

    Ulrych, Jaromír; Krmíček, Lukáš; Tomek, Č.; Lloyd, F. E.; Ladenberger, A.; Ackerman, Lukáš; Balogh, K.

    2016-01-01

    Roč. 76, č. 1 (2016), s. 77-93 ISSN 0009-2819 Institutional support: RVO:67985831 Keywords : Bohemian Massif * Cenozoic alkaline volcanism * Geochemistry * K-Ar ages * Sr-Nd-Pb isotopes Subject RIV: DD - Geochemistry Impact factor: 1.380, year: 2016

  3. Rubidium-strontium and uranium-lead isotopic age studies

    International Nuclear Information System (INIS)

    Loveridge, W.D.

    1981-01-01

    The results of five Rb-Sr isotopic age studies predominantly on whole-rock samples, and six U-Pb studies on zircon monazite concentrates are presented. Descriptions of the geological problems and interpretations of the measured ages are included. Laboratory age determination methods and techniques are described or referenced

  4. Clumped-isotope geochemistry of carbonates: A new tool for the reconstruction of temperature and oxygen isotope composition of seawater

    Energy Technology Data Exchange (ETDEWEB)

    Bernasconi, Stefano M., E-mail: Stefano.bernasconi@erdw.ethz.ch [Geological Institute, ETH Zuerich, Sonneggstrasse 5, 8092 Zuerich (Switzerland); Schmid, Thomas W.; Grauel, Anna-Lena [Geological Institute, ETH Zuerich, Sonneggstrasse 5, 8092 Zuerich (Switzerland); Mutterlose, Joerg [Institut fuer Geologie, Mineralogie und Geophysik, Ruhr Universitaet Bochum, Universitaetsstr. 150, 44801 Bochum (Germany)

    2011-06-15

    Highlights: > Clumped-isotope thermometry of carbonates is discussed. > Clumped isotopes of Belemnites show higher sea surface temperatures than commonly assumed for the lower Cretaceous. > The potential of clumped-isotope measurement on foraminifera is discussed. - Abstract: Clumped-isotope geochemistry deals with State of ordering of rare isotopes in molecules, in particular with their tendency to form bonds with other rare isotopes rather than with the most abundant ones. Among its possible applications, carbonate clumped-isotope thermometry is the one that has gained most attention because of the wide potential of applications in many disciplines of the earth sciences. In particular, it allows reconstructing the temperature of formation of carbonate minerals without knowledge of the isotopic composition of the water from which they were formed. In addition, the O isotope composition of the waters from which they were formed can be calculated using the {delta}{sup 18}O of the same carbonate sample. This feature offers new approaches in paleoclimatology for reconstructing past global geochemical cycles. In this contribution two applications of this method are presented. First the potential of a new analytical method of measurement of clumped isotopes on small samples of foraminifera, for high-resolution SST and seawater {delta}{sup 18}O reconstructions from marine sediments is shown. Furthermore the potential of clumped isotope analysis of belemnites, for reconstructing seawater {delta}{sup 18}O and temperatures in the Cretaceous is shown.

  5. Isotopic composition of strontium in three basalt-andesite centers along the Lesser Antilles arc

    Science.gov (United States)

    Hedge, C.E.; Lewis, J.F.

    1971-01-01

    Si87/Sr86 ratios have been determined for lavas and py lastic rocks from three basalt-andesite centers along the Lesser Antilles arc-Mt. Misery on the island of St. Kitts, Soufriere on the island of St. Vincent, and Carriacou, an island of The Grenadines. The average Si87/Sr86 content of these rocks is 0.7038 for Mt. Misery, 0.7041 for Soufriere, and 0.7053 for Carriacou. All the Sr87/Sr86 values from each center are the same within analytical uncertainty (??0.0002). The constancy of strontium isotopic data within each center supports the hypothesis that basalts and andesites for each specific center investigated are generated from the same source - in agreement with petrographic and major- and minor-element data. Strontium isotopic compositions and elemental concentrations, particularly of strontium and nickel, indicate that this source was mantle peridotite and that the relationship between the respective basalts and andesites is probably fractional crystallization. ?? 1971 Springer-Verlag.

  6. Nuclear charge radii of proton-rich strontium isotopes

    International Nuclear Information System (INIS)

    Eastham, D.A.; Walker, P.M.; Smith, J.R.H.; Warner, D.D.; Griffith, J.A.R.; Evans, D.E.; Wells, S.A.; Fawcett, M.J.; Grant, I.S.

    1987-01-01

    A new technique of atom-photon coincidence laser spectroscopy has been developed and used to study the isotope shifts of /sup 78-84/Sr. The results show that neither the droplet model nor existing interacting boson model calculations can adequately describe the rapid onset of nuclear deformation below N = 50. The odd-even staggering of the charge radius is found to be opposite to that normally encountered, indicating the possible existence of permanent octupole distortions

  7. Strontium isotope study of coal utilization by-products interacting with environmental waters.

    Science.gov (United States)

    Spivak-Birndorf, Lev J; Stewart, Brian W; Capo, Rosemary C; Chapman, Elizabeth C; Schroeder, Karl T; Brubaker, Tonya M

    2012-01-01

    Sequential leaching experiments on coal utilization by-products (CUB) were coupled with chemical and strontium (Sr) isotopic analyses to better understand the influence of coal type and combustion processes on CUB properties and the release of elements during interaction with environmental waters during disposal. Class C fly ash tended to release the highest quantity of minor and trace elements-including alkaline earth elements, sodium, chromium, copper, manganese, lead, titanium, and zinc-during sequential extraction, with bottom ash yielding the lowest. Strontium isotope ratios ((87)Sr/(86)Sr) in bulk-CUB samples (total dissolution of CUB) are generally higher in class F ash than in class C ash. Bulk-CUB ratios appear to be controlled by the geologic source of the mineral matter in the feed coal, and by Sr added during desulfurization treatments. Leachates of the CUB generally have Sr isotope ratios that are different than the bulk value, demonstrating that Sr was not isotopically homogenized during combustion. Variations in the Sr isotopic composition of CUB leachates were correlated with mobility of several major and trace elements; the data suggest that arsenic and lead are held in phases that contain the more radiogenic (high-(87)Sr/(86)Sr) component. A changing Sr isotope ratio of CUB-interacting waters in a disposal environment could forecast the release of certain strongly bound elements of environmental concern. This study lays the groundwork for the application of Sr isotopes as an environmental tracer for CUB-water interaction. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

  8. Strontium isotope detection of brine contamination in the East Poplar oil field, Montana

    Science.gov (United States)

    Peterman, Zell E.; Thamke, Joanna N.; Futa, Kiyoto; Oliver, Thomas A.

    2010-01-01

    Brine contamination of groundwater in the East Poplar oil field was first documented in the mid-1980s by the U.S. Geological Survey by using hydrochemistry, with an emphasis on chloride (Cl) and total dissolved solids concentrations. Supply wells for the City of Poplar are located downgradient from the oil field, are completed in the same shallow aquifers that are documented as contaminated, and therefore are potentially at risk of being contaminated. In cooperation with the Office of Environmental Protection of the Fort Peck Tribes, groundwater samples were collected in 2009 and 2010 from supply wells, monitor wells, and the Poplar River for analyses of major and trace elements, including strontium (Sr) concentrations and isotopic compositions. The ratio of strontium-87 to strontium-86 (87Sr/86Sr) is used extensively as a natural tracer in groundwater to detect mixing among waters from different sources and to study the effects of water/rock interaction. On a plot of the reciprocal strontium concentration against the 87Sr/86Sr ratio, mixtures of two end members will produce a linear array. Using this plotting method, data for samples from most of the wells, including the City of Poplar wells, define an array with reciprocal strontium values ranging from 0.08 to 4.15 and 87Sr/86Sr ratios ranging from 0.70811 to 0.70828. This array is composed of a brine end member with an average 87Sr/86Sr of 0.70822, strontium concentrations in excess of 12.5 milligrams per liter (mg/L), and chloride concentrations exceeding 8,000 mg/L mixing with uncontaminated water similar to that in USGS06-08 with 18.0 mg/L chloride, 0.24 mg/L strontium, and a 87Sr/86Sr ratio of 0.70811. The position of samples from the City of Poplar public-water supply wells within this array indicates that brine contamination has reached all three wells. Outliers from this array are EPU-4G (groundwater from the Cretaceous Judith River Formation), brine samples from disposal wells (Huber 5-D and EPU 1-D

  9. Strontium isotope evidence for a highly mobile population on the Pamir Plateau 2500 years ago

    Science.gov (United States)

    Wang, Xueye; Tang, Zihua; Wu, Jing; Wu, Xinhua; Wu, Yiqun; Zhou, Xinying

    2016-10-01

    Archeological researches have proposed arguments for human mobility and long-distance trading over the Eurasia before the Silk Roads. Here we utilize biologically available strontium isotope analysis to assess the extent of pre-Silk Road population movements and cultural communications across the Asian interior. From an early Iron Age cemetery (ca. 2500 yr B.P.) on the eastern Pamir Plateau, mean 87Sr/86Sr ratios from 34 individuals display considerable isotopic variability, and 10 individuals are distinguished as migrants based on the local strontium isotope range of 0.710296-0.710572 defined by 12 ovicaprine bones. Comparison of the proportion (10/34) with the regional census data completed in 1909 A.D. (3% non-locals) suggests a highly migratory behavior on the plateau 2500 years ago. Furthermore, exotic mortuary objects, such as silk fabrics from eastern China and angular harp originated from the Near East, clearly demonstrate an interaction between different cultures on the plateau before the establishment of the Silk Road.

  10. Strontium-isotope composition in the Tethys Sea, Euboea, Greece

    International Nuclear Information System (INIS)

    Tremba, E.L.; Faure, G.; Summerson, C.H.

    1975-01-01

    The 37 Sr/ 36 Sr ratios of the Tethys Sea have been determined by analyzing limestones of Permian to Late Cretaceous age from the overthrusted sequence of central and northern Euboea. The results are in satisfactory agreement with ratios obtained by other investigators on unreplaced fossil shells of similar age collected elsewhere. The 37 Sr/ 36 Sr ratios of Mesozoic marbles from the autochtone metamorphic rocks of southern Euboea are more variable, perhaps because of increases in this ratio during regional metamorphism. Nevertheless, the lowest values of suites of isochronous samples may approach the correct ratio. Four samples of the Argyron Marble taken at different localities in southern Euboea and on the Attic peninsula have a concordant 87 Sr/ 86 Sr ratio of 0.70688+-0.00006 relative to 0.7080 for the Eimer and Amend isotope standard. This value indicates a Jurassic age for this formation even though the fragmentary fossil evidence favors a Late Cretaceous (Turonian) age

  11. A new method of accurate determination of isotopic composition and concentration of strontium in a spike solution used for geochronological works

    International Nuclear Information System (INIS)

    Yanagi, Takeru

    1990-01-01

    A new method of accurate determination of isotopic composition and concentration of a strontium-84 spike solution was devised for simultaneous determination of strontium contents and isotopic compositions in rocks and minerals by measuring strontium isotopic ratios in spiked samples. In this method, the isotopic composition of strontium in the spike were determined so as to minimize the sum of squares of deviations of spike strontium-84 concentrations which were calculated from measured isotopic ratios of strontium in five different mixtures of the spike and the standard solution. The method can eliminate all mass discriminations occurred during the measurements on a surface ionization mass spectrometer. The results were tested by measuring 87 Sr/ 86 Sr ratios of Eimer and Amend SrCO 3 and JB-1 geochemical reference material, and by determining the strontium content in JB-1. The measurements of strontium isotope ratios in spiked samples give average values of 0.708007±0.000052 and 0.70417±0.00004 for 87 Sr/ 86 Sr ratios of E and A SrCO 3 and JB-1, respectively. The strontium content in JB-1 was estimated at 457.1±1.3 ppm. These values are very close to reported respective values. (author)

  12. Stable isotope geochemistry of the Tongonan geothermal system, Leyte, Philippines

    International Nuclear Information System (INIS)

    Hulston, J.R.; Stewart, M.K.

    1982-01-01

    Stable isotope and geochemical data on samples from natural features, shallow wells and deep wells collected over a number of years from the Tongonan area of Leyte have been evaluated. The variations in the isotopic compositions of the thermal waters are used to describe natural processes occurring within the system. The effect of the ''excess enthalpy'' of the deep wells on the isotope data is formulated. Water from the deep Tongonan wells shows an oxygen-18 shift of 5 per mille, which is larger than at Wairakei and Broadlands, probably in part because of the high temperatures at Tongonan. Recent measurements indicate that the deuterium shift is very much smaller than previously thought. Isotopic measurements of methane in the gases suggests differing flows from the Eastern and Central Philippine faults

  13. Isotopic and noble gas geochemistry in geothermal research

    Energy Technology Data Exchange (ETDEWEB)

    Kennedy, B.M.; DePaolo, D.J. [Lawrence Berkeley National Lab., CA (United States)

    1997-12-31

    The objective of this program is to provide, through isotopic analyses of fluids, fluid inclusions, and rocks and minerals coupled with improved methods for geochemical data analysis, needed information regarding sources of geothermal heat and fluids, the spatial distribution of fluid types, subsurface flow, water-rock reaction paths and rates, and the temporal evolution of geothermal systems. Isotopic studies of geothermal fluids have previously been limited to the light stable isotopes of H, C, and O. However, other isotopic systems such as the noble gases (He, Ne, Ar, Kr and Xe) and reactive elements (e.g. B, N, S, Sr and Pb) are complementary and may even be more important in some geothermal systems. The chemistry and isotopic composition of a fluid moving through the crust will change in space and time in response to varying chemical and physical parameters or by mixing with additional fluids. The chemically inert noble gases often see through these variations, making them excellent tracers for heat and fluid sources. Whereas, the isotopic compositions of reactive elements are useful tools in characterizing water-rock interaction and modeling the movement of fluids through a geothermal reservoir.

  14. Oxygen isotope geochemistry of The Geysers reservoir rocks, California

    Energy Technology Data Exchange (ETDEWEB)

    Gunderson, Richard P.; Moore, Joseph N.

    1994-01-20

    Whole-rock oxygen isotopic compositions of Late Mesozoic graywacke, the dominant host rock at The Geysers, record evidence of a large liquid-dominated hydrothermal system that extended beyond the limits of the present steam reservoir. The graywackes show vertical and lateral isotopic variations that resulted from gradients in temperature, permeability, and fluid composition during this early liquid-dominated system. All of these effects are interpreted to have resulted from the emplacement of the granitic "felsite" intrusion 1-2 million years ago. The {delta}{sup 18}O values of the graywacke are strongly zoned around a northwest-southeast trending low located near the center of and similar in shape to the present steam system. Vertical isotopic gradients show a close relationship to the felsite intrusion. The {delta}{sup 18}O values of the graywacke decrease from approximately 15 per mil near the surface to 4-7 per mil 300 to 600 m above the intrusive contact. The {delta}{sup 18}O values then increase downward to 8-10 per mil at the felsite contact, thereafter remaining nearly constant within the intrusion itself. The large downward decrease in {delta}{sup 18}O values are interpreted to be controlled by variations in temperature during the intrusive event, ranging from 150{degree}C near the surface to about 425{degree}C near the intrusive contact. The upswing in {delta}{sup 18}O values near the intrusive contact appears to have been caused by lower rock permeability and/or heavier fluid isotopic composition there. Lateral variations in the isotopic distributions suggests that the effects of temperature were further modified by variations in rock permeability and/or fluid-isotopic composition. Time-integrated water:rock ratios are thought to have been highest within the central isotopic low where the greatest isotopic depletions are observed. We suggest that this region of the field was an area of high permeability within the main upflow zone of the liquid

  15. The geochemistry of the stable isotopes of silicon

    International Nuclear Information System (INIS)

    Douthitt, C.B.

    1982-01-01

    One hundred thirty two new measurements of the relative abundances of the stable isotopes of silicon in terrestrial materials are presented. The total variation of delta 30 Si found is 6.2 parts per thousand, centered on the mean of terrestrial mafic and ultramafic igneous rocks, delta 30 Si = -0.4 parts per thousand. Igneous rocks show limited variation; coexisting minerals exhibit small, systematic silicon isotopic fractionations that are roughly 1/3 the magnitude of concomitant oxygen isotopic fractionations at 1150 0 C. In both igneous minerals and rocks, delta 30 Si shows a positive correlation with silicon content, as does delta 18 O. Opal from both sponge spicules and sinters is light, with delta 30 Si = -2.3 and -1.4 parts per thousand respectively. Large delta 30 Si values of both positive and negative sign are reported for the first time from clay minerals, opaline phytoliths, and authigenic quartz. All highly fractionated samples were precipitated from solution at low temperatures; however, aqueous silicon is not measurably fractionated relative to quartz at equilibrium. A kinetic isotope fractionation of approximately 3.5 parts per thousand is postulated to occur during the low temperature precipitation of opal and, possibly, poorly ordered phyllosilicates, with the silicate phase being enriched in 28 Si. This fractionation, coupled with a Rayleigh precipitation model, is capable of explaining most non-magmatic delta 30 Si variations. (author)

  16. Strontium and neodymium isotopic compositions in sediments from Godavari, Krishna and Pennar rivers

    International Nuclear Information System (INIS)

    Masood Ahmad, S.; Padmakumari, V.M.; Anil Babu, G.

    2009-01-01

    We report here strontium (Sr) and neodymium (Nd) isotopic compositions in bed sediments from the Godavari, Krishna and Pennar rivers, draining into the Bay of Bengal. The isotopic compositions of these sediments range from 0.7190 to 0.7610 for 87 Sr/ 86 Sr and -12.04 to -23.68 for ε Nd . This wide range in Sr and Nd isotopes is derived from variable proportions of sediments from different rock types in their drainage basins. All the three rivers have their characteristic isotopic signatures. The results display highest 87 Sr/ 86 Sr (0.7610) and most negative ε Nd values (-23.68) for the sediments of Pennar river. This is attributed to the chemical weathering of gneisses and granites in its drainage basin. The 87 Sr/ 86 Sr and ε Nd values for the Godavari river sediments range from 0.7196 to 0.7210 and -15.31 to -18.22 respectively. 87 Sr/ 86 Sr and ε Nd values in Krishna river sediments lie from 0.7217 to 0.7301 and -12.04 to -12.78 respectively. Our results show that the sedimentary load from the Godavari and Krishna rivers is primarily derived from the older rocks in their drainage basins. It is possible that the sediments transported through peninsular Indian rivers predominantly control Sr and Nd isotope sedimentary budget in the western Bay of Bengal. (author)

  17. New Carbonate Standard Reference Materials for Boron Isotope Geochemistry

    Science.gov (United States)

    Stewart, J.; Christopher, S. J.; Day, R. D.

    2015-12-01

    The isotopic composition of boron (δ11B) in marine carbonates is well established as a proxy for past ocean pH. Yet, before palaeoceanographic interpretation can be made, rigorous assessment of analytical uncertainty of δ11B data is required; particularly in light of recent interlaboratory comparison studies that reported significant measurement disagreement between laboratories [1]. Well characterised boron standard reference materials (SRMs) in a carbonate matrix are needed to assess the accuracy and precision of carbonate δ11B measurements throughout the entire procedural chemistry; from sample cleaning, to ionic separation of boron from the carbonate matrix, and final δ11B measurement by multi-collector inductively coupled plasma mass spectrometry. To date only two carbonate reference materials exist that have been value-assigned by the boron isotope measurement community [2]; JCp-1 (porites coral) and JCt-1 (Giant Clam) [3]. The National Institute of Standards and Technology (NIST) will supplement these existing standards with new solution based inorganic carbonate boron SRMs that replicate typical foraminiferal and coral B/Ca ratios and δ11B values. These new SRMs will not only ensure quality control of full procedural chemistry between laboratories, but have the added benefits of being both in abundant supply and free from any restrictions associated with shipment of biogenic samples derived from protected species. Here we present in-house δ11B measurements of these new boron carbonate SRM solutions. These preliminary data will feed into an interlaboratory comparison study to establish certified values for these new NIST SRMs. 1. Foster, G.L., et al., Chemical Geology, 2013. 358(0): p. 1-14. 2. Gutjahr, M., et al., Boron Isotope Intercomparison Project (BIIP): Development of a new carbonate standard for stable isotopic analyses. Geophysical Research Abstracts, EGU General Assembly 2014, 2014. 16(EGU2014-5028-1). 3. Inoue, M., et al., Geostandards and

  18. Isotope geochemistry of water in Gulf Coast Salt Domes

    International Nuclear Information System (INIS)

    Knauth, L.P.; Kumar, M.B.; Martinez, J.D.

    1980-01-01

    Water found as active leaks and isolated pools in the Weeks Island, Jefferson Island, and Belle Isle salt mines of south Louisiana has delta 18 O values ranging from -4 to +11.5% 0 and deltaD values from -2.3 to -53% 0 . One sample from Weeks Island and one from Jefferson Island are isotopically similar to local surface waters and are clearly of meteoric origin. All other samples are too enriched in 18 O to be meteoric waters. In the Weeks Island mine the isotopic data define a linear array given by deltaD=3.0delta 18 O-40.1. Active leaks define the positive end of this array. Isolated pools are interpreted as inactive leaks with initial delta 18 O and deltaD values of +9.1 +- 0.5% 0 and -11% 0 +- 7% 0 , which have subsequently exchanged with water vapor in the mine air to produce the linear array of delta values. The water derived from active leaks in these three mines is too enriched in 18 O and too depleted in D to be connate ocean water or evaporite connate water trapped in the salt. Isotopic composition of water derived from the dehydration of gypsum is probably dissimilar to that of the active leaks. It is unlikely that the water has originated from the dehydration of gypsum. It is also unlikely that isotopic exchange with anhydrite is responsible for observed 18 O enrichments. Nonmeteroric water from the active leaks displays the type of 18 O enrichments characteristic of saline formation waters, where water exchanges isotopically with calcite and clay minerals. It is concluded that the nonmeteoric waters are formation waters which have become incorporated in the salt. From the observed 18 O enrichment it is calculated that formation waters were incorporated during diapiric rise of the salt at a depth of 3--4 km and have been trapped within the salt for 10--13 m.y. Large volumes of salt within salt domes are not naturally penetrated by meteoric groundwaters but can contain limited amounts of trapped formation water

  19. Dendritic network models: Improving isoscapes and quantifying influence of landscape and in-stream processes on strontium isotopes in rivers

    Science.gov (United States)

    Brennan, Sean R.; Torgersen, Christian E.; Hollenbeck, Jeff P.; Fernandez, Diego P.; Jensen, Carrie K.; Schindler, Daniel E.

    2016-05-01

    A critical challenge for the Earth sciences is to trace the transport and flux of matter within and among aquatic, terrestrial, and atmospheric systems. Robust descriptions of isotopic patterns across space and time, called "isoscapes," form the basis of a rapidly growing and wide-ranging body of research aimed at quantifying connectivity within and among Earth's systems. However, isoscapes of rivers have been limited by conventional Euclidean approaches in geostatistics and the lack of a quantitative framework to apportion the influence of processes driven by landscape features versus in-stream phenomena. Here we demonstrate how dendritic network models substantially improve the accuracy of isoscapes of strontium isotopes and partition the influence of hydrologic transport versus local geologic features on strontium isotope ratios in a large Alaska river. This work illustrates the analytical power of dendritic network models for the field of isotope biogeochemistry, particularly for provenance studies of modern and ancient animals.

  20. Isotope geochemistry of sulfur in forest soils and in new groundwater below forest soils

    International Nuclear Information System (INIS)

    Mayer, B.

    1993-04-01

    The isotope geochemistry of sulphur in aerobic forest soils and new groundwater below forest soils was investigated for the purpose of investigating the transport and transformation behaviour of sulfate in the water-unsaturated zone. The effects of hydrodynamic and biogeochemical processes on the development of seepage water sulfate isotopes between depositions and groundwater were investigated by means of laboratory experiments, profile studies, lysimeter experiments, and field studies in order to determine the sulphur conversion processes. Dissolved sulphur from precipitates, seepage water, creek water and groundwater, as well as sulphur extracted from soil samples, were precipitated in the form of BaSO 4 or AgS 2 , decomposed thermally into SO 2 or CO 2 , and the 34 S/ 32 S and 18 O/ 16 O isotope ratios were determined by mass spectrometry. (orig.) [de

  1. Barium isotope geochemistry of subduction-zone magmas

    Science.gov (United States)

    Yu, H.; Nan, X.; Huang, J.; Wörner, G.; Huang, F.

    2017-12-01

    Subduction zones are crucial tectonic setting to study material exchange between crust and mantle, mantle partial melting with fluid addition, and formation of ore-deposits1-3. The geochemical characteristics of arc lavas from subduction zones are different from magmas erupted at mid-ocean ridges4, because there are addition of fluids/melts from subducted AOC and its overlying sediments into their source regions in the sub-arc mantle4. Ba is highly incompatible during mantle melting5, and it is enriched in crust (456 ppm)6 relative to the mantle (7.0 ppm)7. The subducted sediments are also enriched in Ba (776 ppm of GLOSS)8. Moreover, because Ba is fluid soluble during subduction, it has been used to track contributions of subduction-related fluids to arc magmas9 or recycled sediments to the mantle10-11. To study the Ba isotope fractionation behavior during subduction process, we analyzed well-characterized, chemically-diverse arc lavas from Central American, Kamchatka, Central-Eastern Aleutian, and Southern Lesser Antilles. The δ137/134Ba of Central American arc lavas range from -0.13 to 0.24‰, and have larger variation than the arc samples from other locations. Except one sample from Central-Eastern Aleutian arc with obviously heavy δ137/134Ba values (0.27‰), all other samples from Kamchatka, Central-Eastern Aleutian, Southern Lesser Antilles arcs are within the range of OIB. The δ137/134Ba is not correlated with the distance to trench, partial melting degrees (Mg#), or subducting slab-derived components. The samples enriched with heavy Ba isotopes have low Ba contents, indicating that Ba isotopes can be fractionated at the beginning of dehydration process with small amount of Ba releasing to the mantle wedge. With the dehydration degree increasing, more Ba of the subducted slab can be added to the source of arc lavas, likely homogenizing the Ba isotope signatures. 1. Rudnick, R., 1995 Nature; 2. Tatsumi, Y. & Kogiso, T., 2003; 3. Sun, W., et al., 2015 Ore

  2. Strontium isotopes as natural tracers in reservoir oilfield and in groundwater systems

    International Nuclear Information System (INIS)

    Santos, Marcos E.; Palmieri, Helena E.L.; Moreira, Rubens M.

    2009-01-01

    The radioactive beta (β - ) decay of 87 Rb to 87 Sr is an important isotope system that has been widely applied for geochronological purposes and in identifying ground water sources, aquifer interactions and as a tracer for a secondary recovery process in offshore oilfields via seawater injection. The 87 Sr/ 86 Sr ratio of present seawater is constant worldwide, while formation waters in hydrocarbon reservoirs have various values are in most cases higher than modern seawater. This can be the basis for a natural tracer technique aiming at evaluating the performance of seawater injection processes by evaluating the 87 Sr/ 86 Sr ratio and the total Sr content of formation waters in the reservoir prior to injection, followed by monitoring these values in the produced water as injection proceeds. Inductively Couple Plasma Mass Spectrometry ICP-MS is a technique that has potential to be used in studies with tracers in the environment in the determination of isotope ratios and element traces in a sample. This work describes the methodology that will be used for the determination of variations in the isotopic composition of Sr and presents the preliminary results obtained determination of the strontium isotope ratios ( 87 Sr/ 86 Sr) using Inductively Coupled Plasma Mass Spectrometry (ICP-MS). (author)

  3. Paleoclimatic and paleoceanographic studies of estuarine and marine sediments using strontium isotopes

    International Nuclear Information System (INIS)

    Ingram, B.L.

    1992-01-01

    Strontium isotopic ratio ( 87 Sr/ 86 Sr) measurements in fossil carbonates and phosphates are used to evaluate paleoceanographic and paleoclimatic environments in Quaternary, Pliocene-Pleistocene, and mid-Cretaceous estuarine and marine sediments. The use of 87 Sr/ 86 Sr measurements as an estuarine paleosalinity and paleoclimatic indicator is developed and applied to San Francisco Bay. 87 Sr/ 86 Sr measurements of foraminifer and molluscan fossils contained in estuarine sediments of late Pleistocene (ca 115 to 125 ka) and late Holocene (4.5 ka) age show cyclic variations indicating that salinity fluctuated with periods of several hundred years, probably reflecting wet-dry cycles associated with fluctuations in solar irradiance caused by sunspot cycles. The average salinity in San Pablo and Richardson bays was significantly lower (by 6 to 8%) over much of the past 4.5 ka than at present, reflecting a combination of decreased freshwater inflow at present associated with water diversion and wetter climatic conditions prior to 2000 years ago. Salinity data are converted to river discharge using salinity-delta flow relations derived from historical records for San Francisco Bay. The data indicate that annual freshwater inflow was at least twice the modern pre-diversion average between 2.5 and 3.0 Ka; this time period is also identified as one of wetter climatic conditions by lake level and treeline records from the Sierra Nevada. Strontium isotopic measurements of marine carbonate and fish teeth to middle Cretaceous age are used to increase the resolution of the existing seawater Sr isotope versus time curve and to assess models for global oceanic anoxic events. The new data using fish teeth show less scatter and variability than previous data. Negative excursions in the 87 Sr/ 86 Sr ratio of 7-14 parts in 10 -5 during Aptian anoxic events suggest a link between increased submarine volcanism and oceanic anoxia

  4. Hydrogeochemistry and isotope geochemistry of Velenje Basin groundwater

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    Tjaša Kanduč

    2016-08-01

    Full Text Available The geochemical and isotopic composition of groundwater in the Velenje Basin, Slovenia, was investigated between the years 2014 to 2015 to identify the geochemical processes in the major aquifers (Pliocene and Triassic and the water–rock interactions. Thirty-eight samples of groundwater were taken from the aquifers, 19 in the mine and 19 from the surface. Groundwater in the Triassic aquifer is dominated by HCO3–, Ca2+ and Mg2+ with δ13C DIC values in the range from -19.3 to -2.8 ‰, indicating degradation of soil organic matter and dissolution of carbonate minerals. In contrast, groundwater in the Pliocene aquifers is enriched in Mg2+, Na+, Ca2+, K+, and Si, and has high alkalinity, with δ13CDIC values in the range of -14.4 to +4.6 ‰. Based on the δ13CDIC values in all the aquifers (Pliocene and Triassic, both processes inflence the dissolution of carbonate minerals and dissolution of organic matter and in the Pliocene aquifers, methanogenesis as well. Based on Principal Component Analysis (PCA, and on geochemical and isotopic data we conclude that the following types of groundwater in Velenje Basin are present: Triassic aquifers with higher pH and lower conductivity and chloride, Pliocene, Pliocene 1 and Pliocene 2 aquifers with lower pH and higher conductivity and chloride contents, and Pliocene 3 and Pliocene 2, 3 aquifers with the highest pH values and lowest conductivities and chloride contents. 87Sr/86Sr tracer was used for the fist time in Slovenia to determine geochemical processes (dissolution of silicate versus carbonate fraction in Velenje Basin groundwater of different aquifers dewatering Pliocene and Triassic strata. 87Sr/86Sr values range from 0.70820 to 0.71056 in groundwater of Pliocene aquifers and from 0.70808 to 0.70910 in groundwater of the Triassic aquifer. This indicates that dissolution of the carbonate fraction prevails in both aquifers, while in Pliocene aquifers, an additional silicate weathering prevails with

  5. Geographic variation of strontium and hydrogen isotopes in avian tissue: implications for tracking migration and dispersal.

    Directory of Open Access Journals (Sweden)

    Megan J Sellick

    Full Text Available Isotopes can provide unique solutions to fundamental problems related to the ecology and evolution of migration and dispersal because prior movements of individuals can theoretically be tracked from tissues collected from a single capture. However, there is still remarkably little information available about how and why isotopes vary in wild animal tissues, especially over large spatial scales.Here, we describe variation in both stable-hydrogen (deltaD(F and strontium ((87Sr/(86Sr(F isotopic compositions in the feathers of a migratory songbird, the Tree Swallow (Tachycineta bicolor, across 18 sampling sites in North America and then examine potential mechanisms driving this variation. We found that deltaD(F was correlated with latitude of the sampling site, whereas (87Sr/(86Sr(F was correlated with longitude. deltaD(F was related to deltaD of meteoric waters where molting occurred and (87Sr/(86Sr(F was influenced primarily by the geology in the area where feathers were grown. Using simulation models, we then assessed the utility of combining both markers to estimate the origin of individuals. Using 13 geographic regions, we found that the number of individuals correctly assigned to their site of origin increased from less than 40% using either deltaD or (87Sr/(86Sr alone to 74% using both isotopes.Our results suggest that these isotopes have the potential to provide predictable and complementary markers for estimating long-distance animal movements. Combining isotopes influenced by different global-scale processes may allow researchers to link the population dynamics of animals across large geographic ranges.

  6. Integrated modelling of enhanced in situ biodenitrification in a fractured aquifer: biogeochemistry and isotope geochemistry

    Science.gov (United States)

    Rodríguez-Escales, Paula; Folch, Albert; van Breukelen, Boris M.; Vidal-Gavilan, Georgina; Soler, Albert

    2014-05-01

    Enhanced in-situ biodenitrification is a feasible technology to recovery groundwater polluted by nitrates and achieves drinking water standards. Under optimum conditions, nitrate is reduced by autochthonous bacteria trough different reactions until arrive to harmless dinitrogen gas. Isotopic fractionation monitoring in field applications allows knowing the exact degree and the real scope of this technology. Using the Rayleigh equation the change in the isotope ratio of the nitrate molecule (δ15N-NO3-, δ18O-NO3-) is related to the fraction of molecules remaining as a result of biodenitrification. However, Rayleigh application at field scale is sometimes limited due to other processes involved during groundwater flow such as dispersion or adsorption and geological media heterogeneities that interferes in concentration values. Then, include isotope fractionation processes in reactive transport models is a useful tool to interpret and predict data from in-situ biodenitrification. We developed a reactive transport model of enhanced in situ application at field scale in a fractured aquifer that considers biogeochemical processes as well as isotope fractionation to enable better monitoring and management of this technology. Processes considered were: microbiological- exogenous and endogenous nitrate and sulfate respiration coupled with microbial growth and decay, geochemical reactions (precipitation of calcite) and isotopic fractionation (δ15N-NO3-; δ18O- NO3- and carbon isotope network). The 2-D simulations at field scale were developed using PHAST code. Modeling of nitrate isotope geochemistry has allowed determining the extent of biodenitrification in model domain. We have quantified which is the importance in decreasing of nitrate concentrations due to biodegradation (percentage of biodegradation, 'B%') and due to dilution process (percentage of dilution, 'D%'). On the other hand, the stable carbon isotope geochemistry has been modeled. We have considered the

  7. Scale of human mobility in the southern Andes (Argentina and Chile): A new framework based on strontium isotopes.

    Science.gov (United States)

    Barberena, Ramiro; Durán, Víctor A; Novellino, Paula; Winocur, Diego; Benítez, Anahí; Tessone, Augusto; Quiroga, María N; Marsh, Erik J; Gasco, Alejandra; Cortegoso, Valeria; Lucero, Gustavo; Llano, Carina; Knudson, Kelly J

    2017-10-01

    The goal of this article is to assess the scale of human paleomobility and ecological complementarity between the lowlands and highlands in the southern Andes during the last 2,300 years. By providing isotope results for human bone and teeth samples, we assess a hypothesis of "high residential mobility" suggested on the basis of oxygen isotopes from human remains. We develop an isotopic assessment of human mobility in a mountain landscape combining strontium and oxygen isotopes. We analyze bone and teeth samples as an approach to life-history changes in spatial residence. Human samples from the main geological units and periods within the last two millennia are selected. We present a framework for the analysis of bioavailable strontium based on the combination of the geological data with isotope results for rodent samples. The 87 Sr/ 86 Sr values from human samples indicate residential stability within geological regions along life history. When comparing strontium and oxygen values for the same human samples, we record a divergent pattern: while δ 18 O values for samples from distant regions overlap widely, there are important differences in 87 Sr/ 86 Sr values. Despite the large socio-economic changes recorded, 87 Sr/ 86 Sr values indicate a persisting scenario of low systematic mobility between the different geological regions. Our results suggest that strontium isotope values provide the most germane means to track patterns of human occupation of distinct regions in complex geological landscapes, offering a much higher spatial resolution than oxygen isotopes in the southern Andes. © 2017 Wiley Periodicals, Inc.

  8. Strontium isotope evolution of pore water and calcite in the Topopah Spring Tuff, Yucca Mountain, Nevada

    International Nuclear Information System (INIS)

    Marshall, Brian D.; Futa, Kiyoto

    2001-01-01

    Pore water in the Topopah Spring Tuff has a narrow range of (delta) 87 Sr values that can be calculated from the (delta) 87 Sr values of the rock considering advection through and reaction with the overlying nonwelded tuffs of the PTn. This model can be extended to estimate the variation of (delta) 87 Sr in the pore water through time; this approximates the variation of (delta) 87 Sr measured in calcite fracture coatings. In samples of calcite where no silica can be dated by other methods, strontium isotope data may be the only method to determine ages. In addition, other Sr-bearing minerals in the calcite and opal coatings, such as fluorite, may be dated using the same model

  9. Nuclear moments and isotopic variation of the mean square charge radii of strontium nuclei by atomic beam laser spectroscopy

    International Nuclear Information System (INIS)

    Chongkum, S.

    1987-10-01

    Hyperfine structure and optical isotope shift measurements have been performed on a series of stable and radioactive strontium isotopes (A = 80 to 90), including two isomers 85m and 87m. The spectroscopy applied continuous wave dye laser induced fluorescence of free atoms at λ=293.2 nm in a well collimated atomic beam. The 293.2 nm ultraviolet light was generated by frequency doubling the output of a dye laser in either a temperature tuned Ammonium Dihydrogen Arsenate (ADA) crystal or an angle tuned Lithium Iodate crystal. A special radio frequency (rf) technique was used to tune the dye laser frequency with long term stability. Radioactive Sr isotopes were produced either by neutron capture of stable strontium or by (α,xn) reactions from krypton gas. The samples were purified by an electromagnetic mass separator and their sizes were of order 100 pg, which corresponds to 10 11 atoms. The observed results of the hyperfine structure components are evaluated in terms of nuclear magnetic dipole moments and electric quadrupole moments. Changes in mean square charge radii of strontium nuclei which were extracted from the isotope shift measurements, exhibit a distinct shell effect at the neutron magic number N=50. The experimental data are analysed and compared with some theoretical nuclear model predictions. The strong increase of the nuclear charge radii with decreasing neutron number of isotopes below N=50 is in agreement with the variation of the mean square deformation extracted from measured B(E2) values. (orig.) [de

  10. The temperature dependent strontium isotope fractionation (δ88/86Sr) during calcium carbonate precipitation

    International Nuclear Information System (INIS)

    Fietzke, J.; Eisenhauer, A.

    2006-01-01

    Full text: In order to study the influence of stable isotope fractionation during inorganic and biologically controlled CaCO 3 precipitation we have developed the analytical principles for the measurement of strontium (Sr) isotope fractionation. We have established a measurement protocol for the application on a MC-ICP-MS (AXIOM) using the common bracketing standard technique. The Sr-standard CRM NBS987 was used as reference material for all measurements and to calculate the Sr fractionation. Latter value is expressed by the δ-notation defined as: δ 88/86 Sr = [( 88 Sr/ 86 Sr)sample / ( 88 Sr/ 86 Sr)standard ] * 1000 -1. A first set of experiments focused on the temperature dependency of Sr-isotope fractionation. For this purpose inorganically precipitated aragonite and calcite was prepared under controlled conditions in a temperature range from 10 to 50 o C. In addition, cultured and naturally grown corals were analyzed for their δ 88/86 Sr values. Repeated measurements of IAPSO seawater standard showed a mean δ 88/86 Sr value of 0.383 ± 0.008 (2 SEM) being the isotopically heaviest material measured so far. The first results of the inorganically precipitated aragonite and the natural corals revealed a clear temperature dependency of the δ 88/86 Sr values. For inorganic aragonite the slope of this correlation is about 0.0055 permil/ o C. However, for naturally grown corals (Pavona clavus) a 6 fold steeper slope of 0.033 permil/ o C was determined. This strong temperature dependency implies the potential to use stable Sr isotopes as a new marine (paleo)temperature proxy. (author)

  11. Isotope hydrology and geochemistry of northern Chile groundwaters

    Directory of Open Access Journals (Sweden)

    1995-01-01

    Full Text Available HYDROLOGIE ISOTOPIQUE ET GEOCHIMIE DES EAUX SOUTERRAINES DU NORD CHILI. Cet article est un résumé des études de caractérisation d’aquifères situés dans la Pampa del Tamarugal et du Salar de Atacama au nord du Chili à l’aide d’isotopes. Les objectifs principaux de ces études étaient d’obtenir de l’information sur l’origine et le temps de résidence des eaux souterraines, la qualité des eaux, les taux d’évaporation des salars et la relation entre les inondations et la recharge des aquifères. Les principales conclusions de ces études sont les suivantes: a la majorité de l’eau souterraine est de bonne qualité à l’exception des zones situées près des salars b un système multi-aquifère a été identifié dans le bassin de la Pampa del Tamaragual en relation avec des zones de recharges situées à différentes altitudes et c une importante portion des eaux souterraines dans les aquifères de la Pampa devraient êtres considérées comme une ressource non renouvelable. HIDROLOGÍA ISOTÓPICA Y GEOQUÍMICA DE LAS AGUAS SUBTERRÁNEAS DEL NORTE DE CHILE. En este trabajo se presenta un resumen de estudios que se han realizado en el Norte de Chile, en acuíferos localizados en la Pampa del Tamarugal y en el Salar de Atacama. Los principales objetivos de esos estudios fueron obtener información sobre el origen y el tiempo de residencia del agua subterránea, calidad química del agua, tasas de evaporación desde los salares y evaluar la relación entre inundaciones y recarga a los acuíferos. Las principales conclusiones de estos estudios fueron las siguientes: a la mayoría del agua subterránea es de buena calidad, con la excepción de las áreas cercanas a los salares b se identificó en la cuenca de la Pampa del Tamarugal un sistema de multiacuífero relacionado a áreas de recargas localizadas en diferentes altitudes c una parte importante del agua subterránea en la Pampa del Tamarugal tiene que ser tratada como un recurso

  12. Summary of theory and techniques, sample selection and project organization for potassium-argon, rubidium-strontium and fission track dating and strontium isotope studies

    International Nuclear Information System (INIS)

    Adams, C.J.; Graham, I.J.; Seward, D.

    1987-02-01

    A brief outline is given of the theory and techniques of the potassium-argon, rubidium-strontium and fission-track dating methods and related isotope studies which are currently in use at the Institute of Nuclear Sciences, DSIR. Some limitations of each technique are set out in terms of age range and materials for dating, and the appropriate choice of various mineral and rock types and subsequent age interpretations are discussed. The organisation of project proposals and categories is described and procedures for sample submission and documentation are given

  13. Strontium isotopes provide clues for a process shift in base cation dynamics in young volcanic soils

    Science.gov (United States)

    Bingham, N.; Jackson, M. G.; Bookhagen, B.; Maher, K.; Chadwick, O.

    2015-12-01

    Despite advances in soil development theory based on studies of old soils or over long timescales, little is known about soil thresholds (dramatic changes in soil properties associated with only small shifts in external forcing factors) that might be expressed in young soils (less than 10 kyr). Therefore, we seek to understand infant soil development in a tropical environment through the sourcing of plant available base cations by measuring the strontium (Sr) isotopic composition of the soil exchange complex. Our sampling strategy spans soils in three different precipitation ranges (950-1060 mm, 1180-1210 mm, and 1450-1500) and an array of soil ages from 500 to 7500 years in the Kona region on the island of Hawaii. In Hawaiian soils, 87Sr/86Sr values are determined by a mixture of three components: a mantle-derived component from the lava (0.7034), a rainfall component (0.7093) and a component from continental dust (0.720). Elevation-controlled leaching intensity in the wettest localities produces a decline in the concentration of base cations supplied by basalt and a dilute resupply by rainfall. In the driest sites, where leaching intensity is dramatically reduced, there is a buildup of rainfall-derived extractable Sr in the soil over time. Slow rock weathering rates produce a small rock-derived cation input to the soil. Thus, Sr isotope signatures reflect both the input of rainfall-derived cations and rock-derived cations with values that fall between rainfall and basaltic signatures. Soils in the intermediate precipitation range have Sr isotopic signatures consistent with both the wet and dry trends; suggesting that they lie close to the critical precipitation amount that marks a shift between these two processes. For the Kona region, this transition seems to occur at 1200 mm /yr. In contrast to the clear-cut differentiation in strontium isotopes with precipitation shifts observed in older soils, patterns on these young soils in Kona are complicated by low soil

  14. STRONTIUM ISOTOPE STRATIGRAPHY AS A CONTRIBUTION FOR DATING MIOCENE SHELF CARBONATES (S. MARINO FM., NORTHERN APENNINES

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    CLAUDIO ARGENTINO

    2017-01-01

    Full Text Available This paper provides new data on strontium isotope stratigraphy applied to the Miocene heterozoan shelfal carbonates of the S. Marino Fm. (Marecchia Valley, northern Apennines. Sr isotopic analyses were carried out on oyster shells, bryozoans and bulk-rocks from the lower-middle carbonate portion of the section. In the upper part of the succession that shows evidence of detrital influx,87Sr/86Sr analyses were performed on foraminifera tests, separating planktonic and benthic forms. Results were compared with calcareous nannofossil biostratigraphic data from the same levels, in order to test the reliability of Sr dating in mixed carbonate-siliciclastic sediments. Mean ages obtained from oysters range between 16.9 Ma and 16.3 Ma. Very similar results are obtained using bryozoans (16.5 Ma to 16.1 Ma and bulk-rocks (16.8 Ma to 16.2 Ma. These results allow to better constrain the age of the massive carbonate shelf, referable to the upper Burdigalian. In the upper carbonate-siliciclastic portion of the shelf, numerical ages obtained from planktonic and benthic foraminifera are in good agreement with nannofossil biozones (mean ages respectively around 15.3 Ma and 14.5 Ma although they display wide confidence intervals. These wide age uncertainties depend on the slow rate of change of marine 87Sr/86Sr through time that characterizes the interval between ~15 and ~13.5 Ma.

  15. Strontium isotope evidence on the history of oilfield brines, Mediterranean Coastal Plain, Israel

    International Nuclear Information System (INIS)

    Starinsky, A.; Bielski, M.; Lazar, B.; Steinitz, G.; Raab, M.

    1983-01-01

    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 87 Sr/ 86 Sr ratios from 0.7075 to 0.7090. E and A = 0.7081 +- 0.0004 (2σ). The brines are classified into two groups: (a) Mavqi'im group - brines with relatively high 87 Sr/ 86 Sr ratios, sampled from clastics, dolomites and anhydrites of Upper Miocene age. (b) Heletz group - brines with relatively low 87 Sr/ 86 Sr ratios, sampled from sandstones and dolomites of Lower Cretaceous age. Equations were derived to show the relations between 87 Sr/ 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 87 Sr/ 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 87 Sr/ 86 Sr ratios could have been developed. (author)

  16. Estimation of groundwater velocities from Yucca Flat to the Amargosa Desert using geochemistry and environmental isotopes

    International Nuclear Information System (INIS)

    Hershey, R.L.; Acheampong, S.Y.

    1997-06-01

    Geochemical and isotopic data from groundwater sampling locations can be used to estimate groundwater flow velocities for independent comparison to velocities calculated by other methods. The objective of this study was to calculate groundwater flow velocities using geochemistry and environmental isotopes from the southern end of Yucca Flat to the Amargosa Desert, considering mixing of different groundwater inputs from sources each and southeast of the Nevada Test Site (NTS). The approach used to accomplish the objective of this study consisted of five steps: (1) reviewing and selecting locations where carbon isotopic groundwater analyses, reliable ionic analysis, and well completion information are available; (2) calculating chemical speciation with the computer code WATEQ4F (Ball and Nordstrom, 1991) to determine the saturation state of mineral phases for each ground water location; (3) grouping wells into reasonable flowpaths and mixing scenarios from different groundwater sources; (4) using the computer code NETPATH (Plummer et al., 1991) to simulate mixing and the possible chemical reactions along the flowpath, and to calculate the changes in carbon-13/carbon-12 isotopic ratios (δ 13 C) as a result of these reactions; and (5) using carbon-14 ( 14 C) data to calculate velocity

  17. Application of heavy stable isotopes in forensic isotope geochemistry: A review

    International Nuclear Information System (INIS)

    Aggarwal, Jugdeep; Habicht-Mauche, Judith; Juarez, Chelsey

    2008-01-01

    Light stable isotopes have been used for many years to characterize the source and transport of materials. More recently heavy isotope systems such as Sr, Nd and Pb have been added to this list in order to aid source identification. With the advent of multiple collector ICP-MS, the range of isotopic tools now available has increased considerably, however, until the isotope systematics of these new non-traditional isotope systems have become better understood, they will not be as useful in characterizing material source and transportation. Applications using heavy metal stable isotopes (mostly traditional heavy isotopes) have reached most avenues in science, including earth sciences, archaeology, anthropology, animal physiology, ecology and toxicology. This field will continue to grow as new applications are developed and techniques become simpler and quicker. This paper provides a review of how this field has grown and presents two new applications using Pb and Sr isotopes in glazes to determine the source of ore used in glazes, and using Sr isotopes to determine the origin of undocumented deceased Mexican border crossers

  18. Application of heavy stable isotopes in forensic isotope geochemistry: A review

    Energy Technology Data Exchange (ETDEWEB)

    Aggarwal, Jugdeep [W.M. Keck Isotope Laboratory, Department of Earth Sciences, University of California, Santa Cruz, CA 95064 (United States)], E-mail: jaggarwal@pmc.ucsc.edu; Habicht-Mauche, Judith; Juarez, Chelsey [Department of Anthropology, University of California, Santa Cruz, CA 95064 (United States)

    2008-09-15

    Light stable isotopes have been used for many years to characterize the source and transport of materials. More recently heavy isotope systems such as Sr, Nd and Pb have been added to this list in order to aid source identification. With the advent of multiple collector ICP-MS, the range of isotopic tools now available has increased considerably, however, until the isotope systematics of these new non-traditional isotope systems have become better understood, they will not be as useful in characterizing material source and transportation. Applications using heavy metal stable isotopes (mostly traditional heavy isotopes) have reached most avenues in science, including earth sciences, archaeology, anthropology, animal physiology, ecology and toxicology. This field will continue to grow as new applications are developed and techniques become simpler and quicker. This paper provides a review of how this field has grown and presents two new applications using Pb and Sr isotopes in glazes to determine the source of ore used in glazes, and using Sr isotopes to determine the origin of undocumented deceased Mexican border crossers.

  19. Synopsis of strontium isotope variations in groundwater at Aspo, southern Sweden

    Science.gov (United States)

    Peterman, Z.E.; Wallin, B.

    1999-01-01

    Strontium isotope ratios are used to identify end-member ground-water compositions at Aspo in southeastern Sweden where the Hard Rock Laboratory (HRL) has been constructed to evaluate the suitability of crystalline rock for the geologic disposal of nuclear waste. The Hard Rock Laboratory is a decline (tunnel) constructed in 1.8 Ga-old granitic rock that forms islands in an archipelago along the Swedish coast. Ground-water samples were obtained for isotopic analyses from boreholes drilled from the surface and from side boreholes drilled within the HRL. Infiltration at Aspo occurs primarily through fractures zones in the granitic bedrock beneath thin soils throughout the area. Because of extremely low Sr concentrations, rain and snow are not important contributors to the Sr isotope budget of the ground-water system. At shallow levels, water percolating downward along fractures and fracture zones acquires a ??87Sr between +9.5 and +10.0??? and maintains this value downward while Sr concentrations increase by two orders of magnitude. Ground-water samples from both boreholes and from in the HRL show the effects of mixing with saline waters containing as much as 59 mg/L Sr and ??87Sr values as large as +13.92%, Baltic Sea water is a potential component of the groundwater system with ??87Sr values only slightly larger than modern marine values (+0.3???) but with much lower concentrations (1.5 mg/L) than ocean water (8 mg/L). However, because of large Sr concentration differences between the saline groundwater (59 mg/L) and Baltic Sea water (1.5 rag/L), ??87Sr values are not particularly sensitive indicators of sea-water intrusion even though their ??87Sr values differ substantially.

  20. Strontium isotopic signatures of oil-field waters: Applications for reservoir characterization

    Science.gov (United States)

    Barnaby, R.J.; Oetting, G.C.; Gao, G.

    2004-01-01

    The 87Sr/86Sr compositions of formation waters that were collected from 71 wells producing from a Pennsylvanian carbonate reservoir in New Mexico display a well-defined distribution, with radiogenic waters (up to 0.710129) at the updip western part of the reservoir, grading downdip to less radiogenic waters (as low as 0.708903 to the east. Salinity (2800-50,000 mg/L) displays a parallel trend; saline waters to the west pass downdip to brackish waters. Elemental and isotopic data indicate that the waters originated as meteoric precipitation and acquired their salinity and radiogenic 87Sr through dissolution of Upper Permian evaporites. These meteoric-derived waters descended, perhaps along deeply penetrating faults, driven by gravity and density, to depths of more than 7000 ft (2100 m). The 87 Sr/86Sr and salinity trends record influx of these waters along the western field margin and downdip flow across the field, consistent with the strong water drive, potentiometric gradient, and tilted gas-oil-water contacts. The formation water 87Sr/86Sr composition can be useful to evaluate subsurface flow and reservoir behavior, especially in immature fields with scarce pressure and production data. In mature reservoirs, Sr Sr isotopes can be used to differentiate original formation water from injected water for waterflood surveillance. Strontium isotopes thus provide a valuable tool for both static and dynamic reservoir characterization in conjunction with conventional studies using seismic, log, core, engineering, and production data. Copyright ??2004. The American Association of Petroleum Geologist. All rights reserved.

  1. Study on strontium isotope abundance-ratio measurements by using a 13-MeV proton beam

    Science.gov (United States)

    Jeong, Cheol-Ki; Jang, Han; Lee, Goung-Jin

    2016-09-01

    The Rb-Sr dating method is used in dating Paleozoic and Precambrian rocks. This method measures the 87Rb and the 87Sr concentrations by using thermal ionization mass spectrometry (TIMS) [J. Hefne et al., Inter. J. Phys. Sci. 3(1), 28 (2008)]. In addition, it calculates the initial 87Sr/86Sr ratio to increase the reliability of Rb-Sr dating. In this study, the 87Sr/86Sr ratio was measured by using a 13-MeV proton accelerator. Proton kinetic energies are in the range of tens of megaelectronvolts, and protons have large absorption cross-sections for ( p, n) reactions with most substances. After absorbing a proton with such a high kinetic energy, an element is converted into a nuclide with its atomic number increased by one via nuclear transmutation. These nuclides usually have short half-lives and return to the original state through radioactive decay. When a strontium sample is irradiated with protons, nuclear transmutation occurs; thus, the strontium isotope present in the sample changes to a yttrium isotope, which is an activated radioisotope. Based on this, the 87Sr/86Sr ratio was calculated by analyzing the gamma-rays emitted by each yttrium isotope. The KIRAMS-13 cyclotron at the Cyclotron Center of Chosun University, where 13-MeV protons can be extracted, was utilized in our experiment. The 87Sr/86Sr isotope ratio was computed for samples irradiated with these protons, and the result was similar to the isotope ratio for the Standard Reference Material, i.e., 98.2 ± 3.4%. As part of the analysis, proton activation analyses were performed using 13-MeV protons, and the experimental results of this research suggest a possible approach for measuring the strontium-isotope abundance ratio of samples.

  2. Strontium isotope geochemistry of late cretaceous granodiorites, Jamaica and Haiti, Greater Antilles

    International Nuclear Information System (INIS)

    Jones, L.M.; Walker, R.L.; Kesler, S.E.; Lewis, J.F.

    1979-01-01

    Initial 87 Sr/ 86 Sr ratios have been determined for a representative suite of Upper Cretaceous granodiorites and associated rocks from the Above Rocks composite stock in central Jamaica and the Terre-Neuve pluton in northwestern Haiti. The average initial 87 Sr/ 86 Sr ratio for seven samples of the Terre-Neuve intrusion is 0.7036, with a range of 0.7026-0.7047. For two samples of the Above Rocks the initial ratios are 0.7033 and 0.7034. A third sample from this intrusive has an initial ratio of 0.7084, which is tentatively attributed to contamination. The initial 87 Sr/ 86 Sr ratios indicate that neither ancient sialic crust nor sediments carried down a Benioff zone can be the primary source of the granodioritic magma. K/Rb ratios for these rocks range from 178 to 247, which are much lower than the average values (>= 1000) for tholeiitic basalts. It is concluded that the magmas originated primarily by melting of downthrust oceanic crust or adjacent mantle material. (Auth.)

  3. Genesis of hydrothermal alterations using stable isotope geochemistry in Takestan area (Tarom zone

    Directory of Open Access Journals (Sweden)

    Batool Taghipou

    2015-12-01

    Full Text Available Hydrothermal alteration processes are extensively took place on volcanic and pyroclstics of Takestan area. Existence of abundant, deep fracturing and subvolcanic intrusions are enhanced extend hydrothermal alteration zones. The following alteration zones are determined: propylitic, argillic, advanced argillic and sillicic. There are outcropped and widespread in different size and limit. Formation of siliceous sinter, silicified tuffs with preserved primary sedimentary layering including pure mineralized alunite patches are most outstanding. Quartz, sussoritic plagioclase, chlorite, sericite and alunite are main mineral constituents in the volcanics. On the basis of geochemical data volcanic rocks are rhyolite, dacite, andesite, andesitic-basalt and basalt in composition. Acid-sulfate zone is the type of alteration in Tarom area and alunite is an index mineral of this zone. Results of 18O, D and 34S stable isotope geochemistry on altered minerals (muscovite, kaolinite and alunite, revealed that alteration fluids are magmatic in origin.

  4. A routine high-precision method for Lu-Hf isotope geochemistry and chronology

    Science.gov (United States)

    Patchett, P.J.; Tatsumoto, M.

    1981-01-01

    A method for chemical separation of Lu and Hf from rock, meteorite and mineral samples is described, together with a much improved mass spectrometric running technique for Hf. This allows (i) geo- and cosmochronology using the176Lu???176Hf+??- decay scheme, and (ii) geochemical studies of planetary processes in the earth and moon. Chemical yields for the three-stage ion-exchange column procedure average 90% for Hf. Chemical blanks are international mass spectrometric standard; suitable aliquots, prepared from a single batch of JMC 475, are available from Denver. Lu-Hf analyses of the standard rocks BCR-1 and JB-1 are given. The potential of the Lu-Hf method in isotope geochemistry is assessed. ?? 1980 Springer-Verlag.

  5. Mapping and defining sources of variability in bioavailable strontium isotope ratios in the Eastern Mediterranean

    Science.gov (United States)

    Hartman, Gideon; Richards, Mike

    2014-02-01

    The relative contributions of bedrock and atmospheric sources to bioavailable strontium (Sr) pools in local soils was studied in Northern Israel and the Golan regions through intensive systematic sampling of modern plants and invertebrates, to produce a map of modern bioavailable strontium isotope ratios (87Sr/86Sr) for regional reconstructions of human and animal mobility patterns. The study investigates sources of variability in bioavailable 87Sr/86Sr ratios, in particular the intra-and inter-site range of variation in plant 87Sr/86Sr ratios, the range of 87Sr/86Sr ratios of plants growing on marine sedimentary versus volcanic geologies, the differences between ligneous and non-ligneous plants with varying growth and water utilization strategies, and the relative contribution of atmospheric Sr sources from different soil and vegetation types and climatic zones. Results indicate predictable variation in 87Sr/86Sr ratios. Inter- and intra-site differences in bioavailable 87Sr/86Sr ratios average of 0.00025, while the range of 87Sr/86Sr ratios measured regionally in plants and invertebrates is 0.7090 in Pleistocene calcareous sandstone and 0.7074 in mid-Pleistocene volcanic pyroclast. The 87Sr/86Sr ratios measured in plants growing on volcanic bedrock show time dependent increases in atmospheric deposition relative to bedrock weathering. The 87Sr/86Sr ratios measured in plants growing on renzina soils depends on precipitation. The spacing between bedrock 87Sr/86Sr ratios and plants is highest in wet conditions and decreases in dry conditions. The 87Sr/86Sr ratios measured in plants growing on terra rossa soils is relatively constant (0.7085) regardless of precipitation. Ligneous plants are typically closer to bedrock 87Sr/86Sr ratios than non-ligneous plants. Since the bioavailable 87Sr/86Sr ratios currently measured in the region reflect a mix of both exogenous and endogenous sources, changes in the relative contribution of exogenous sources can cause variation

  6. Development of precise analytical methods for strontium and lanthanide isotopic ratios using multiple collector inductively coupled plasma mass spectrometry

    International Nuclear Information System (INIS)

    Ohno, Takeshi; Takaku, Yuichi; Hisamatsu, Shun'ichi

    2007-01-01

    We have developed precise analytical methods for strontium and lanthanide isotopic ratios using multiple collector-ICP-mass spectrometry (MC-ICP-MS) for experimental and environmental studies of their behavior. In order to obtain precise isotopic data using MC-ICP-MS, the mass discrimination effect was corrected by an exponential law correction method. The resulting isotopic data demonstrated that highly precise isotopic analyses (better than 0.1 per mille as 2SD) could be achieved. We also adopted a de-solvating nebulizer system to improve the sensitivity. This system could minimize the water load into the plasma and provided about five times larger intensity of analyte than a conventional nebulizer system did. (author)

  7. 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)

    Guerrot, C.

    1989-01-01

    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 [fr

  8. Strontium and oxygen isotopic variations in mesozoic and tertiary plutons of central Idaho

    International Nuclear Information System (INIS)

    Fleck, R.J.; Criss, R.E.

    1985-01-01

    Regional variations in initial 87 Sr/ 86 Sr ratios (rsub(i)) of Mesozoic plutons in central Idaho locate the edge of Precambrian continental crust at the boundary between the late Paleozoic-Mesozoic accreted terranes and Precambrian sialic crust in western Idaho. The rsub(i) values increase abruptly but continuously from less than 0.704 in the accreted terranes to greater than 0.708 across a narrow, 5 to 15 km zone, characterized by elongate, lens-shaped, highly deformed plutons and schistose metasedimentary and metavolcanic units. The chemical and petrologic character of the plutons changes concomitantly from ocean-arc-type units to a weakly peraluminous, calcit to calcalkalic suite. Plutons in both suites yield Late Cretaceous ages, but Permian through Early Cretaceous bodies are confined to the accreted terranes and early Tertiary intrusions are restricted to areas underlain by Precambrian crust. The two major terranes were juxtaposed between 75 and 130 m.y. ago, probably between 80 and 95 m.y. Oxygen and strontium isotopic ratios and Rb and Sr concentrations of the plutonic rocks document a significant upper-crustal contribution to the magmas that intrude Precambrian crust. Magmas intruding the arc terranes were derived from the upper mantle/subducted oceanic lithosphere and may have been modified by anatexis of earlier island-arc volcanic and sedimentary units. (orig./PW)

  9. Decorporation of mixture of strontium and cesium isotopes with domestic mineral waters

    International Nuclear Information System (INIS)

    Slavov, S.; Filev, G.; Kiradzhiev, G.

    1990-01-01

    The possibilities of Bulgarian mineral waters to decorporate mixtures of strontium and cesium radioisotopes, simultaneous entering the body, were studied. A modified effect in respect to radioactive strontium was found. Modification of the effect of mixing two diferent types of mineral waters was not proven. No effect was found of potassium-containing mineral water on radioactive cesium kinetics. 1 tab., 7 refs

  10. Late Guadalupian evolution of the Delaware Basin: insights from stable isotope and trace element geochemistry

    Science.gov (United States)

    Smith, B.; Kerans, C.

    2017-12-01

    Accurate characterization of mixed carbonate and evaporite deposits requires an understanding of basin-scale physical, chemical, and biological processes. In these settings, carbonate geochemistry often responds to changes in the prevailing conditions in the water column. It follows that the geochemical record presents a potential aid for interpretation of depositional systems provided that it is relatively free of diagenetic overprint. This is seldom the case in shallow-water settings as processes such as meteoric diagenesis and early dolomitization obscure or erase the original geochemical signal. Fine grained deep-water sediments are more likely to retain their original geochemical characteristics. If reliable shelf-to-basin correlations can be established, then basinal deposits provide critical data not only for the interpretation of deep water environments, but overall basin evolution as well. This study examines variations in trace element and stable isotope geochemistry from the Delaware Basin of West Texas and New Mexico. Interpretation of geochemical data within a pre-existing shelf-to-basin stratigraphic framework suggests a link between basin water chemistry and sea level changes during the entirety of the Guadalupian. This link is supported analogies to modern silled basins where changes in sea level and thus recharge across the sill can control nutrient input, circulation, and bottom water oxygenation. In light of these relationships, the filling of the Delaware Basin with basin-centered evaporites at the end of the Guadalupian likely represents the culmination of a more gradual, cyclic evolution towards basin restriction. Ongoing work will continue to focus on tying regional-scale changes in basin water chemistry to the combined geochemical and physical sedimentological records.

  11. PLANETARY-SCALE STRONTIUM ISOTOPIC HETEROGENEITY AND THE AGE OF VOLATILE DEPLETION OF EARLY SOLAR SYSTEM MATERIALS

    Energy Technology Data Exchange (ETDEWEB)

    Moynier, Frederic; Podosek, Frank A. [Department of Earth and Planetary Science and McDonnell Center for Space Sciences, Washington University, St. Louis, MO 63130 (United States); Day, James M. D. [Geosciences Research Division, Scripps Institution of Oceanography, La Jolla, CA 92093-0244 (United States); Okui, Wataru; Yokoyama, Tetsuya [Department of Earth and Planetary Sciences, Tokyo Institute of Technology, Tokyo 152-8551 (Japan); Bouvier, Audrey [Department of Earth Sciences, University of Minnesota, Minneapolis, MN 55455-0231 (United States); Walker, Richard J., E-mail: moynier@levee.wustl.edu, E-mail: fap@levee.wustl.edu, E-mail: jmdday@ucsd.edu, E-mail: rjwalker@umd.edu, E-mail: okui.w.aa@m.titech.ac.jp, E-mail: tetsuya.yoko@geo.titech.ac.jp, E-mail: abouvier@umn.edu [Department of Geology, University of Maryland, College Park, MD 20742 (United States)

    2012-10-10

    Isotopic anomalies in planetary materials reflect both early solar nebular heterogeneity inherited from presolar stellar sources and processes that generated non-mass-dependent isotopic fractionations. The characterization of isotopic variations in heavy elements among early solar system materials yields important insight into the stellar environment and formation of the solar system, and about initial isotopic ratios relevant to long-term chronological applications. One such heavy element, strontium, is a central element in the geosciences due to wide application of the long-lived {sup 87}Rb-{sup 87}Sr radioactive as a chronometer. We show that the stable isotopes of Sr were heterogeneously distributed at both the mineral scale and the planetary scale in the early solar system, and also that the Sr isotopic heterogeneities correlate with mass-independent oxygen isotope variations, with only CI chondrites plotting outside of this correlation. The correlation implies that most solar system material formed by mixing of at least two isotopically distinct components: a CV-chondrite-like component and an O-chondrite-like component, and possibly a distinct CI-chondrite-like component. The heterogeneous distribution of Sr isotopes may indicate that variations in initial {sup 87}Sr/{sup 86}Sr of early solar system materials reflect isotopic heterogeneity instead of having chronological significance, as interpreted previously. For example, given the differences in {sup 84}Sr/{sup 86}Sr between calcium aluminum inclusions and eucrites ({epsilon}{sup 84}Sr > 2), the difference in age between these materials would be {approx}6 Ma shorter than previously interpreted, placing the Sr chronology in agreement with other long- and short-lived isotope systems, such as U-Pb and Mn-Cr.

  12. Isotopic strontium, carbon and oxygen study on neoproterozoic marbles from Sierra de Umango, Andean Foreland, Argentina

    International Nuclear Information System (INIS)

    Varela, R; Valencio, S.; Ramos, A; Sato, K; Gonzalez, P; Panarello, H; Roverano, D

    2001-01-01

    The Umango Hill (La Rioja Province, 29 o 00'S-68 o 40'W) is one of the mountain blocks of Sierras Pampeanas Occidentales (Caminos, 1979), bounded by thrust faults and surrounded by Upper Devonian to Tertiary marine and continental sedimentites. The exposed crystalline basement is composed of basic igneous rocks and a siliciclastic-limestone sequence, both affected by amphibolite facies metamorphic peak. In the southern area (Juchi creek), the metamorphic complex carries relics of granitic orthogneisses, with Rb/Sr and U/Pb dates of ∼1000 Ma (Varela et al., 1996). These ancient inliers were asigned to a Mesoproterozoic Grenville Orogenic Cycle. Granitic bodies, intrusives at different ages in the Metamorphic Complex, have also been distinguished. The most ancient is El Penon Granite, with 469±9 Ma Rb/Sr age (Varela et al., 2000) and 523±26 Ma U/Pb zircon age (unpublished data). In this way it is possible to point out broadly that the siliciclastic-limestone sequence belongs to the Neoproterozoic-Early Palaeozoic times. It was a platform cover over grenvillian cratonic basement. The metamorphism and deformation, we understand, took place in the Early Palaeozoic, related to the Pampean-Famatinian Orogenic Cycle. In this work, compositional and isotopic data of Strontium ( 87 Sr/ 86 Sr), Carbon (δ 13 Cv PDB ) and Oxygen (δ 18 Ov PDB ) of the marbles derived from the siliciclastic-limestone sequence are presented. The results are interpreted and correlated with the temporal variation curves of 87 Sr/ 86 Sr and δ 13 C from Neoproterozoic marine carbonates (Jacobsen and Kaufman, 1999) (au)

  13. Hydrologic and environmental controls on uranium-series and strontium isotope ratios in a natural weathering environment

    Science.gov (United States)

    White, A. M.; Ma, L.; Moravec, B. G.; McIntosh, J. C.; Chorover, J.

    2017-12-01

    In a remote, volcanic headwater catchment of the Jemez River Basin Critical Zone Observatory (JRB-CZO) in NM, stable water isotopes and solute chemistry have shown that snowmelt infiltrates and is stored before later discharging into springs and streams via subsurface flowpaths that vary seasonally. Therefore, water-rock reactions are also expected to change with season as hydrologic flowpaths transport water, gases and solutes through different biogeochemical conditions, rock types and fracture networks. Uranium-series isotopes have been shown to be a novel tracer of water-rock reactions and source water contributions while strontium isotopes are frequently used as indicators of chemical weathering and bedrock geology. This study combines both isotopes to understand how U and Sr isotope signatures evolve through the Critical Zone (CZ). More specifically, this work examines the relationship between seasonality, water transit time (WTT), and U-series and Sr isotopes in stream and spring waters from three catchments within the JRB-CZO, as well as lithology, rock type and CZ structure in solid phase cores. Samples from ten springs with known WTTs were analyzed for U and Sr isotopes to determine the effect of WTT on the isotopic composition of natural waters. Results suggest that WTT alone cannot explain the variability of U and Sr isotopes in JRB-CZO springs. Stream samples were also collected across two water years to establish how seasonality controls surface water isotopic composition. U and Sr isotope values vary with season, consistent with a previous study from the La Jara catchment; however, this study revealed that these changes do not show a systematic pattern among the three catchments suggesting that differences in the mineralogy and structure of the deep CZ in individual catchments, and partitioning of water along deep vs surficial and fracture vs matrix flow paths, likely also control isotopic variability. The distribution of U-series and Sr isotopes in

  14. Automated method for simultaneous lead and strontium isotopic analysis applied to rainwater samples and airborne particulate filters (PM10).

    Science.gov (United States)

    Beltrán, Blanca; Avivar, Jessica; Mola, Montserrat; Ferrer, Laura; Cerdà, Víctor; Leal, Luz O

    2013-09-03

    A new automated, sensitive, and fast system for the simultaneous online isolation and preconcentration of lead and strontium by sorption on a microcolumn packed with Sr-resin using an inductively coupled plasma mass spectrometry (ICP-MS) detector was developed, hyphenating lab-on-valve (LOV) and multisyringe flow injection analysis (MSFIA). Pb and Sr are directly retained on the sorbent column and eluted with a solution of 0.05 mol L(-1) ammonium oxalate. The detection limits achieved were 0.04 ng for lead and 0.03 ng for strontium. Mass calibration curves were used since the proposed system allows the use of different sample volumes for preconcentration. Mass linear working ranges were between 0.13 and 50 ng and 0.1 and 50 ng for lead and strontium, respectively. The repeatability of the method, expressed as RSD, was 2.1% and 2.7% for Pb and Sr, respectively. Environmental samples such as rainwater and airborne particulate (PM10) filters as well as a certified reference material SLRS-4 (river water) were satisfactorily analyzed obtaining recoveries between 90 and 110% for both elements. The main features of the LOV-MSFIA-ICP-MS system proposed are the capability to renew solid phase extraction at will in a fully automated way, the remarkable stability of the column which can be reused up to 160 times, and the potential to perform isotopic analysis.

  15. Evaluating the use of strontium isotopes in tree rings to record the isotopic signal of dust deposited on the Wasatch Mountains

    International Nuclear Information System (INIS)

    Miller, Olivia L.; Solomon, Douglas Kip; Fernandez, Diego P.; Cerling, Thure E.; Bowling, David R.

    2014-01-01

    Highlights: • Dust was a major contributor of Sr to soil and tree rings over Sr poor bedrocks. • Tree rings were evaluated for their use as a record of dust strontium isotope history. • The isotopic signal of dust deposited on the Wasatch Mountains changed over the past ∼75 years. - Abstract: Dust cycling from the Great Basin to the Rocky Mountains is an important component of ecological and hydrological processes. We investigated the use of strontium (Sr) concentrations and isotope ratios ( 87 Sr/ 86 Sr) in tree rings as a proxy for dust deposition. We report Sr concentrations and isotope ratios ( 87 Sr/ 86 Sr) from atmospherically deposited dust, soil, bedrock, and tree rings from the Wasatch Mountains to investigate provenance of dust landing on the Wasatch Mountains and to determine if a dust Sr record is preserved in tree rings. Trees obtained a majority of their Sr from dust, making them a useful record of dust source and deposition. Dust contributions of Sr to soils were more than 94% over quartzite, 63% over granodiorite, and 50% over limestone. Dust contributions of Sr to trees were more than 85% in trees growing over quartzite, 55% over granodiorite, and between 0% and 92% over limestone. These findings demonstrate that a dust signal was preserved in some tree rings and reflects how Sr from dust and bedrock mixes within the soil. Trees growing over quartzite were most sensitive to dust. Changes in Sr isotope ratios for a tree growing over quartzite were interpreted as changes in dust source over time. This work has laid the foundation for using tree rings as a proxy for dust deposition over time

  16. Lithostratigraphy, petrography, biostratigraphy, and strontium-isotope stratigraphy of the surficial aquifer system of western Collier County, Florida

    Science.gov (United States)

    Edwards, L.E.; Weedman, S.D.; Simmons, R.; Scott, T.M.; Brewster-Wingard, G. L.; Ishman, S.E.; Carlin, N.M.

    1998-01-01

    In 1996, seven cores were recovered in western Collier County, southwestern Florida, to acquire subsurface geologic and hydrologic data to support ground-water modeling efforts. This report presents the lithostratigraphy, X-ray diffraction analyses, petrography, biostratigraphy, and strontium-isotope stratigraphy of these cores. The oldest unit encountered in the study cores is an unnamed formation that is late Miocene. At least four depositional sequences are present within this formation. Calculated age of the formation, based on strontium-isotope stratigraphy, ranges from 9.5 to 5.7 Ma (million years ago). An unconformity within this formation that represents a hiatus of at least 2 million years is indicated in the Old Pump Road core. In two cores, Collier-Seminole and Old Pump Road, the uppermost sediments of the unnamed formation are not dated by strontium isotopes, and, based on the fossils present, these sediments could be as young as Pliocene. In another core (Fakahatchee Strand-Ranger Station), the upper part of the unnamed formation is dated by mollusks as Pliocene. The Tamiami Formation overlies the unnamed formation throughout the study area and is represented by the Ochopee Limestone Member. The unit is Pliocene and probably includes the interval of time near the early/late Pliocene boundary. Strontium-isotope analysis indicates an early Pliocene age (calculated ages range from 5.1 to 3.5 Ma), but the margin of error includes the latest Miocene and the late Pliocene. The dinocyst assemblages in the Ochopee typically are not age-diagnostic, but, near the base of the unit in the Collier-Seminole, Jones Grade, and Fakahatchee Strand State Forest cores, they indicate an age of late Miocene or Pliocene. The molluscan assemblages indicate a Pliocene age for the Ochopee, and a distinctive assemblage of Carditimera arata and Chione cortinaria in several of the cores specifically indicates an age near the early/late Pliocene boundary. Undifferentiated sands

  17. Analyses and quantitative determination of the strontium radioisotopes 89 and 90 in milk powder; Recherche et dosage des isotopes radioactifs 89 et 90 du strontium dans le lait en poudre

    Energy Technology Data Exchange (ETDEWEB)

    Jeanmaire, L; Michon, G [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

    1959-07-01

    The authors describe a procedure for the determination of the strontium radioisotopes 89 and 90. The concentration of strontium is made possible by the insolubility of its nitrate salt in strong nitric acid which allows the removal of greatest part of calcium. The purification is performed on a cation exchange column. The amount of radioisotope 90 is determined by means of its daughter product yttrium 90 necessary calibrations and computations are treated in special paragraphs. With regard to the reproducibility of the measurements, the fluctuations are less than 20 per cent. This seems satisfaction for such a technique which have great sensibility while being long and necessitative great carefulness. (author) [French] Les auteurs decrivent une technique de dosage des isotopes 89 et 90 du strontium. La concentration du strontium est assuree grace a l'insolubilite de son nitrate dans l'acide nitrique concentre, ce qui permet d'eliminer la plus grande partie du Ca. La purification se fait sur une colonne echangeuse de cations. L'isotope 90 est dose grace a son descendant l'yttrium 90. Les etalonnages et calculs necessaires font l'objet de paragraphes detailles. En ce qui concerne la reproductibilite des mesures, les fluctuations sont inferieures a 20 pour cent, ce qui semble satisfaisant devant la grande sensibilite de la methode qui reste cependant longue et delicate. (auteur)

  18. Oxygen isotope geochemistry of Laurentide ice-sheet meltwater across Termination I

    Science.gov (United States)

    Vetter, Lael; Spero, Howard J.; Eggins, Stephen M.; Williams, Carlie; Flower, Benjamin P.

    2017-12-01

    We present a new method that quantifies the oxygen isotope geochemistry of Laurentide ice-sheet (LIS) meltwater across the last deglaciation, and reconstruct decadal-scale variations in the δ18O of LIS meltwater entering the Gulf of Mexico between ∼18 and 11 ka. We employ a technique that combines laser ablation ICP-MS (LA-ICP-MS) and oxygen isotope analyses on individual shells of the planktic foraminifer Orbulina universa to quantify the instantaneous δ18Owater value of Mississippi River outflow, which was dominated by meltwater from the LIS. For each individual O. universa shell, we measure Mg/Ca (a proxy for temperature) and Ba/Ca (a proxy for salinity) with LA-ICP-MS, and then analyze the same O. universa for δ18O using the remaining material from the shell. From these proxies, we obtain δ18Owater and salinity estimates for each individual foraminifer. Regressions through data obtained from discrete core intervals yield δ18Ow vs. salinity relationships with a y-intercept that corresponds to the δ18Owater composition of the freshwater end-member. Our data suggest that from 15.5 through 14.6 ka, estimated δ18Ow values of Mississippi River discharge from discrete core intervals range from -11‰ to -21‰ VSMOW, which is consistent with δ18O values from both regional precipitation and the low-elevation, southern margin of the LIS. During the Bølling and Allerød (14.0 through 13.3 ka), estimated δ18Ow values of Mississippi River discharge from discrete core intervals range from -22‰ to -38‰ VSMOW. These values suggest a dynamic melting history of different parts of the LIS, with potential contributions to Mississippi River outflow from both the low-elevation, southern margin of the LIS and high-elevation, high-latitude domes in the LIS interior that were transported to the ablation zone. Prior to ∼15.5 ka, the δ18Owater value of the Mississippi River was similar to that of regional precipitation or low-latitude LIS meltwater, but the Ba

  19. Geochemistry of the Congo and Amazon river systems. Boron isotopic geochemistry in corals. Continental erosion and ocean pH

    International Nuclear Information System (INIS)

    Gaillardet, J.

    1995-01-01

    Two main geological processes control the CO 2 concentration in the atmosphere at a geological time scale: CO 2 outgasing from the interior of the Earth and CO 2 consumption by continental weathering. In the thesis, we initiate two different directions that can be useful to constraint the past climate evolution models. The first one is the extensive study of the largest rivers of the world using the classical geochemical analyses (major and trace elements, Sr-Nd-Pb isotopes) and modelling approaches. The study case of this thesis are the Congo and Amazon Basin. In particular, the coupling between chemical and physical erosion is examined and related to the hydrologic and tectonic parameters. Relief, thus tectonics appear to best control CO 2 consumption by rock weathering. The second part of the work is devoted to the measurement of boron isotopic ratio in corals because it may be used as a proxy for paleo-ocean pH. It could thus bring important pieces of information on the global C cycle and climate evolution. The technical part is extensively described and the method applied to the corals from the last interglacial period. Our conclusion is that corals are likely to be influence by early diagenetic changes that modify the boron isotopic composition of corals. We thus propose a test to select the samples. (author)

  20. Strontium concentrations and isotope ratios in a forest-river system in the South Qinling Mts., China.

    Science.gov (United States)

    Bu, Hongmei; Song, Xianfang; Zhang, Quanfa; Burford, Michele A

    2016-04-15

    The concentrations of dissolved strontium (Sr) and isotope ratios ((87)Sr/(86)Sr) in rainwater, river water, and water from forest soil are measured to investigate the contributions of these sources to a river during base flow conditions in the relatively pristine South Qinling Mountains, China. Dissolved Sr concentrations and (87)Sr/(86)Sr ratios vary significantly between different water types (p water samples including Ca(2+), Mg(2+), EC, and TDS (p water chemistry in the river water. Using the three-source mixing model, atmospheric inputs, carbonate, and silicate weathering contribute 74%, 20%, and 6% respectively to the dissolved Sr in the river water. This research has provided new insights into the contribution of sources of Sr to a river system in a mountainous catchment. Copyright © 2016 Elsevier Ltd. All rights reserved.

  1. The geographic distribution of strontium isotopes in Danish surface waters - A base for provenance studies in archaeology, hydrology and agriculture

    International Nuclear Information System (INIS)

    Frei, Karin M.; Frei, Robert

    2011-01-01

    Research highlights: → Strontium isotope data of 192 surface waters from Denmark. → Geographic baseline distribution of bio-available fractions. → Applicable for provenance studies within archaeology, geology, agriculture and hydrology. → Proposal of a band of strontium isotope values to characterize 'local' Danish signatures. - Abstract: In this paper Sr isotope signatures are reported for 192 surface water (lakes/ponds and rivers/creeks) samples from within Denmark and an isotope distribution map is presented that may serve as a base for provenance applications, including archaeological migration studies, ground water - surface water - seawater interaction/contamination monitoring, and potentially for agricultural applications, including cases of authenticity proof for particular food products. The Sr isotopic compositions of surface waters range from 87 Sr/ 86 Sr = 0.7078 to 0.7125 (average 0.7096 ± 0.0016; 2σ). This average value lies above the range of 87 Sr/ 86 Sr values between 0.7078 and 0.7082 expected from Late Cretaceous to Early Tertiary (Oligocene) limestones which form the dominant bedrock type in a NW-SE trending belt in Denmark. The elevated 87 Sr/ 86 Sr signatures >∼0.7095 are explained by additions to the surface waters of radiogenic Sr predominantly derived from the near-surface weathering and wash-out of Quarternary glaciogenic tills and soils deposited and formed during and after the last two ice age stages (Saale and Weichsel). The Sr isotopic compositions and concentrations of the surface waters can, therefore, best be modeled by a two-component mixing involving carbonaceous bedrock and glaciogenic cover sediments as the two predominant Sr sources. A feasibility study for using Sr isotopic compositions of surface waters as a proxy for bio-available Sr signatures was conducted in a representative test area on Zealand (Land of Legends, Lejre) where there is no use and application of commercial fertilizers. It is demonstrated that

  2. Nannofossil biostratigraphy, strontium and carbon isotope stratigraphy, cyclostratigraphy and an astronomically calibrated duration of the Late Campanian Radotruncana calcarata Zone.

    Science.gov (United States)

    Wagreich, Michael; Hohenegger, Johann; Neuhuber, Stephanie

    2012-12-01

    A section from the southern (Austro-Alpine Northern Calcareous Alps) margin of the Penninic Ocean in the NW Tethys realm of Late Campanian age is investigated stratigraphically. Plankton foraminifer and nannofossil biostratigraphy designate the presence of the Globotruncana ventricosa Zone and the Radotruncana ( Globotruncanita ) calcarata Zone, and standard nannofossil zones CC21-UC15c TP and CC22ab-UC15de TP . The combination of carbon isotope stratigraphy, strontium isotopes, and cyclostratigraphy allows a detailed chronostratigraphic correlation. Periodicity was obtained by power spectral analysis, sinusoidal regression, and Morlet wavelets. The duration of the calcarata Total Range Zone is calculated by orbital cyclicity expressed in thickness data of limestone-marl rhythmites and stable carbon isotope data. Precessional, obliquity, and short and long eccentricity cycles are identified and give an extent of c. 806 kyr for the zone. Mean sediment accumulation rates are as low as 1.99 cm/kyr and correspond well to sediment accumulation rates in similar settings. We further discuss chronostratigraphic implications of our data.

  3. Study the mechanisms of recharge of the phreatic aquifers, south east egypt, using environmental isotopes and hydro geochemistry

    International Nuclear Information System (INIS)

    Hassan, T.M.; Awad, M.A.; Hamza, M.S.

    1994-01-01

    The recharge rate is the most critical factor to groundwater resources management especially in semi-arid and arid areas. This paper presents a study on the feasibility of a groundwater development plan for south east egypt area. Environmental stable isotopes (oxygen-18 and deuterium), and hydro geochemistry techniques were used to investigate the recharge sources of groundwater. The examined groundwater wells tap the quaternary, basement and Nubian sandstone aquifers. The isotopic compositions of these groundwater samples indicate that there is a mixing among three different sources of recharge, local precipitation, palaeo water and sea water intrusion along the coastal plain, from the hydrochemical point of view, the predominant water types reflect meteoric, as well as marine waters genesis. The changes in salinity depend upon the dissolution of terrestrial salts, distance from the catchment area and seepage from deep aquifers. 7 figs., 2 tabs

  4. Different contamination styles of prehistoric human teeth at a Swiss necropolis (Sion, Valais) inferred from lead and strontium isotopes

    International Nuclear Information System (INIS)

    Chiaradia, M.; Gallay, A.; Todt, W.

    2003-01-01

    Separate fractions of dentine and enamel of 12 individuals from the necropolis of Sion (Valais, Switzerland) have been analyzed for Pb and Sr isotope compositions. The individuals span a time period of more than 1 ka from ∼5.2 ka B.P. to ∼4.1 ka B.P. and include Middle Neolithic, Upper Neolithic, Bell Beaker and Old Bronze age civilizations. Individuals were buried either into or close to dolmens or into soil at 4 different sites on the alluvial fan of the Sionne stream, a tributary of the Rhone river. Isotopic composition of dentine and enamel pairs of the individuals indicate that teeth underwent post mortem contamination. Lead contamination is due to two different sources, petrol and natural Pb from soils. The preponderance of either petrol or natural Pb contamination in teeth depends on the burial sites. Differences in the content of Pb-retaining particles (organic matter, Fe-hydroxides, clay minerals), that depend largely on soil grain size, are suggested to be responsible for the differential Pb contamination at the investigated burial sites. Strontium contamination is stronger in individuals buried into or close to dolmens, which are made of calc-schist slabs. Despite post mortem contamination, both Pb and Sr isotopes have allowed the identification of an individual's enamel with isotopic compositions significantly different from those of the local substratum, suggesting his immigration to the Sion area from a geologically different region. This individual belongs to the Bell Beaker civilization, which is considered to have immigrated into Western Europe and the Mediterranean basin at the end of the Neolithic. Systematic differences between enamel and dentine isotopic compositions of all other individuals analyzed suggest that they assimilated in vivo Pb and Sr from an area nearby to that in which they were buried

  5. Comment on: 'The strontium isotopic composition of seawater and seawater-oceanic crust interaction' by E.T.C. Spooner

    International Nuclear Information System (INIS)

    Brass, G.W.; Turekian, K.L.

    1977-01-01

    Various processes have been proposed as the source of strontium to the oceans but there is no evidence to support the mechanism of release of relatively unradiogenic strontium from deep dea basalts to sea-water. (B.D.)

  6. Strontium isotopes reveal distant sources of architectural timber in Chaco Canyon, New Mexico

    OpenAIRE

    English, Nathan B.; Betancourt, Julio L.; Dean, Jeffrey S.; Quade, Jay

    2001-01-01

    Between A.D. 900 and 1150, more than 200,000 conifer trees were used to build the prehistoric great houses of Chaco Canyon, New Mexico, in what is now a treeless landscape. More than one-fifth of these timbers were spruce (Picea) or fir (Abies) that were hand-carried from isolated mountaintops 75–100 km away. Because strontium from local dust, water, and underlying bedrock is incorporated by trees, specific logging sites can be identified by comparing 87Sr/86Sr ratios in construction beams fr...

  7. Do Strontium Isotope Ratios of Animal Bone and Teeth Really Reflect the Isotope Ratios of its birth- and growth-places?

    Science.gov (United States)

    Minami, M.; Goto, A.; Suzuki, K.; Kato, T.; Watanabe, K.; Hasegawa, T.

    2007-12-01

    Strontium enters the human body through the food chain as nutrients pass from bedrock through soil and water to plants and animals. Strontium substitutes for calcium in the hydroxyapatite mineral of skeletal tissue, and is stored there. 87Sr/86Sr ratios in an individual's bone and teeth could directly reflect the isotopic ratios found in the plants and animals that she or he consumed, which reflect the isotope ratios found in the soil and bedrock of that geologic region. Therefore, 87Sr/86Sr ratios of human skeletons could be useful tools for assessing human residential mobility in prehistory, and many studies on them have been often made. In this study, to evaluate whether the 87Sr/86Sr ratio of a bone or teeth really reflects the isotopic ratios of its birth and growth places, several bone and teeth samples were measured for 87Sr/86Sr ratios, compared with 87Sr/86Sr ratios of geological samples in their growth-places. Bone and teeth samples were leached with 5% acetic acid. After drying, samples were ashed in a muffle furnace at 825°C for 8h, and then digested in nitric acid, followed by cation exchange chromatography with 2.4M hydrochloric acid. 87Sr/86Sr ratios were measured using a thermal ionization mass Spectrometer (VG Sector 54) or an inductively coupled plasma mass spectrometer (Finnigan ELEMENT2). A modern boar bone collected at Asuke, Toyota City, Aichi prefecture, Japan showed a 87Sr/86Sr of 0.71001±0.00002 (2 σ), while stream sediments in the Asuke area showed around 0.710 (Asahara et al., 2006). The 87Sr/86Sr ratio of a modern black bass bone collected from Lake Biwa, Shiga prefecture, Japan was 0.71215±0.00002, while those of surface water in Lake Biwa was 0.71233±0.00002. The similar 87Sr/86Sr ratios between bone and its provenance geology could indicate that the 87Sr/86Sr ratios of bones reflect the isotopic ratios of the birth- and growth-places. The more results of modern and fossil skeletons will be shown in our presentation.

  8. Strontium isotope systematics of mixing groundwater and oil-field brine at Goose Lake in northeastern Montana, USA

    Science.gov (United States)

    Peterman, Zell E.; Thamke, Joanna N.; Futa, Kiyoto; Preston, Todd

    2012-01-01

    Groundwater, surface water, and soil in the Goose Lake oil field in northeastern Montana have been affected by Cl−-rich oil-field brines during long-term petroleum production. Ongoing multidisciplinary geochemical and geophysical studies have identified the degree and local extent of interaction between brine and groundwater. Fourteen samples representing groundwater, surface water, and brine were collected for Sr isotope analyses to evaluate the usefulness of 87Sr/86Sr in detecting small amounts of brine. Differences in Sr concentrations and 87Sr/86Sr are optimal at this site for the experiment. Strontium concentrations range from 0.13 to 36.9 mg/L, and corresponding 87Sr/86Sr values range from 0.71097 to 0.70828. The local brine has 168 mg/L Sr and a 87Sr/86Sr value of 0.70802. Mixing relationships are evident in the data set and illustrate the sensitivity of Sr in detecting small amounts of brine in groundwater. The location of data points on a Sr isotope-concentration plot is readily explained by an evaporation-mixing model. The model is supported by the variation in concentrations of most of the other solutes.

  9. Strontium isotopic ratios of Tertiary volcanic rocks of northeastern Honshu, Japan: implication for the spreading of the Japan Sea

    International Nuclear Information System (INIS)

    Kurasawa, Hajime; Konda, Tadashi.

    1986-01-01

    Strontium isotopic ratios of sixty-seven Tertiary volcanic rocks from the northeastern Honshu, Japan, were determined for the purpose of examining the genesis among the volcanic rocks. Two distince suites of volcanic rocks occur in the northeastern Honshu; the rocks older than 16 Ma (Monzen-Daijima Stege) of predominantly intermediate composition and the rocks younger than 16 Ma (Nishikurosawa-Funakawa Stege) with bimodal suite of mafic and felsic composition. Initial values of 87 Sr/ 86 Sr in the Teriary volcanic rocks from the northeastern Honshu, lie in the range from 0.7033 to 0.7068. High ( 87 Sr/ 86 Sr) I ratios are observed for the rocks older than 16 Ma from the Japan Sea side (H zone). It is noteworthy that the rocks younger than 16 Ma show significantly lower ( 87 Sr/ 86 Sr) I ratios in the Dewa Hill, Japan Sea coast and North Akita areas in the northeastern Honshu (L zone). The rocks younger than 16 Ma from the L zone can also be interpreted as having been originated as a mantle-diapir associated with the spreading of the Japan Sea basin. If the basaltic magma was formed from the diapir, the 87 Sr/ 86 Sr ratio would be close to the range from 0.7033 to 0.7037 as the low-Sr isotopic ratio zone (L zone) in the northeastern Honshu, Japan. (author)

  10. Applications of isotope geochemistry to the reconstruction of Yucca Mountain, Nevada, paleohydrology -- Status of investigations: June 1996

    International Nuclear Information System (INIS)

    Whelan, J.F.; Moscati, R.J.; Allerton, S.B.M.; Marshall, B.D.

    1998-01-01

    Tunneling of the Exploratory Studies Facility has offered the opportunity to sample and examine occurrences of secondary mineralization found in the unsaturated-zone tuffs of Yucca Mountain, nevada. Petrographic and paragenetic analyses, calcite and silica-phase stable isotopic analyses, and preliminary strontium tracer isotope and radiocarbon age analyses of these samples indicate that (1) an early stage of secondary mineralization consisting largely of chalcedony and quartz, but possibly with or slightly preceded by calcite, probably formed at warmer than ambient temperatures; (2) later secondary mineralization consisting of calcite and opal appears completely consistent with formation from percolation of surface infiltration whose solute load and carbon isotopic compositions reflect passage through the overlying soils; (3) based on textural studies, all unsaturated-zone secondary mineral occurrences exposed within the Exploratory Studies Facility tunnel, with the exception of the vapor-phase assemblages that formed at high temperatures during cooling of the tuffs, probably formed in unsaturated settings; and (4) calcite radiocarbon ages, based on preliminary results, have not been compromised by post-depositional exchange with carbon-bearing water and gases in the unsaturated zone

  11. Applications of isotope geochemistry to the reconstruction of Yucca Mountain, Nevada, paleohydrology -- Status of investigations: June 1996

    Energy Technology Data Exchange (ETDEWEB)

    Whelan, J.F.; Moscati, R.J.; Allerton, S.B.M.; Marshall, B.D.

    1998-11-01

    Tunneling of the Exploratory Studies Facility has offered the opportunity to sample and examine occurrences of secondary mineralization found in the unsaturated-zone tuffs of Yucca Mountain, nevada. Petrographic and paragenetic analyses, calcite and silica-phase stable isotopic analyses, and preliminary strontium tracer isotope and radiocarbon age analyses of these samples indicate that (1) an early stage of secondary mineralization consisting largely of chalcedony and quartz, but possibly with or slightly preceded by calcite, probably formed at warmer than ambient temperatures; (2) later secondary mineralization consisting of calcite and opal appears completely consistent with formation from percolation of surface infiltration whose solute load and carbon isotopic compositions reflect passage through the overlying soils; (3) based on textural studies, all unsaturated-zone secondary mineral occurrences exposed within the Exploratory Studies Facility tunnel, with the exception of the vapor-phase assemblages that formed at high temperatures during cooling of the tuffs, probably formed in unsaturated settings; and (4) calcite radiocarbon ages, based on preliminary results, have not been compromised by post-depositional exchange with carbon-bearing water and gases in the unsaturated zone.

  12. Strontium isotope fractionation during strontianite (SrCO3) dissolution, precipitation and at equilibrium

    Science.gov (United States)

    Mavromatis, Vasileios; Harrison, Anna L.; Eisenhauer, Anton; Dietzel, Martin

    2017-12-01

    In this study we examine the behavior of stable Sr isotopes between strontianite [SrCO3] and reactive fluid during mineral dissolution, precipitation, and at chemical equilibrium. Experiments were performed in batch reactors at 25 °C in 0.01 M NaCl solutions wherein the pH was adjusted by bubbling of a water saturated gas phase of pure CO2 or atmospheric air. The equilibrium Sr isotope fractionation between strontianite and fluid after dissolution of the solid under 1 atm CO2 atmosphere was estimated as Δ88/86SrSrCO3-fluid = δ88/86Sr SrCO3 - δ88/86Srfluid = -0.05 ± 0.01‰. On the other hand, during strontianite precipitation, an enrichment of the fluid phase in 88Sr, the heavy isotopomer, was observed. The evolution of the δ88/86Srfluid during strontianite precipitation can be modeled using a Rayleigh distillation approach and the estimated, kinetically driven, fractionation factor αSrCO3-fluid between solid and fluid is calculated to be 0.99985 ± 0.00003 corresponding to Δ88/86SrSrCO3-fluid = -0.15‰. The obtained results further support that under chemical equilibrium conditions between solid and fluid a continuous exchange of isotopes occurs until the system approaches isotopic equilibrium. This isotopic exchange is not limited to the outer surface layer of the strontianite crystal, but extends to ∼7-8 unit cells below the crystal surface. The behavior of Sr isotopes in this study is in excellent agreement with the concept of dynamic equilibrium and it suggests that the time needed for achievement of chemical equilibrium is generally shorter compared to that for isotopic equilibrium. Thus it is suggested that in natural Sr-bearing carbonates an isotopic change may still occur close to thermodynamic equilibrium, despite no observable change in aqueous elemental concentrations. As such, a secondary and ongoing change of Sr isotope signals in carbonate minerals caused by isotopic re-equilibration with fluids has to be considered in order to use Sr

  13. Calcium isotope fractionation between aqueous compounds relevant to low-temperature geochemistry, biology and medicine

    OpenAIRE

    Frédéric Moynier; Toshiyuki Fujii

    2017-01-01

    Stable Ca isotopes are fractionated between bones, urine and blood of animals and between soils, roots and leaves of plants by >1000?ppm for the 44Ca/40Ca ratio. These isotopic variations have important implications to understand Ca transport and fluxes in living organisms; however, the mechanisms of isotopic fractionation are unclear. Here we present ab initio calculations for the isotopic fractionation between various aqueous species of Ca and show that this fractionation can be up to 3000?...

  14. Strontium isotopic signature of groundwater from Adamantina aquifer, Bauru Basin, Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Maldaner, Carlos [Centre for Applied Groundwater Research, University of Guelph, 50 Stone Rd, Guelph, ON, N1G 2W1 (Canada); Martins, Veridiana; Bertolo, Reginaldo; Hirata, Ricardo [Centro de Pesquisas de Aguas Subterraneas do Instituto de Geociencias da Universidade de Sao Paulo, Sao Paulo - SP (Brazil)

    2013-07-01

    Using {sup 87}Sr/{sup 86}Sr ratios and the geochemistry of groundwater we were able to identify different hydrochemical facies in the Adamantina aquifer, Bauru Basin (Brazil). Samples from shallow wells show Cl-NO{sub 3}-Ca-Mg water with low pH due to natural and anthropogenic recharge. The {sup 87}Sr/{sup 86}Sr ratios are greatest in the shallower parts of the aquifer (0.7134) and decrease with increasing well screen interval depth. The nitrate concentration gradually decreases with depth and aquifer pH increases, HCO{sub 3} predominates as the main anion, and the groundwater becomes saturated with respect to calcite, with average {sup 87}Sr/{sup 86}Sr ratios of 0.708694 at depth. (authors)

  15. Strontium isotopes reveal weathering processes in lateritic covers in southern China with implications for paleogeographic reconstructions

    Science.gov (United States)

    Wei, Xiao; Wang, Shijie; Ji, Hongbing; Shi, Zhenhua

    2018-01-01

    The isotope ratios of Sr are useful tracers for studying parent material sources, weathering processes, and biogeochemical cycling. Mineralogical and geochemical investigations of two lateritic weathering covers, in an area close to the Tropic of Cancer (Guangxi Province, southern China), were undertaken to study the regional weathering processes and Sr isotopic sources. We found that weathering and decomposition of Rb- and Sr-bearing minerals change the Sr isotopic composition in weathering products (lateritic soils). Weathering of illite lowered the 87Sr/86Sr ratio whereas dissolving and leaching of carbonate minerals increased the 87Sr/86Sr ratio. An Fe nodular horizon is widely developed on the top of the weathering covers in the studied area and it differs from the lateritic soil horizon in mineral composition, construction, and elemental concentration. Furthermore, both Fe2O3 and P2O5 (concentrations) are negatively correlated with the 87Sr/86Sr ratios, suggesting fixation of apatite by Fe oxides is a controlling factor of the Sr isotopic composition in the Fe nodular horizon. The 87Sr/86Sr and Nb/Sr ratios imply the contents and proportions of Fe nodules and clay are critical in controlling the changes of Sr isotopic composition in the Fe nodular horizon. The two stages of the weathering process of carbonate rocks are revealed by the87Sr/86Sr versus Nb/Sr diagram. The 87Sr/86Sr and Rb/Sr ratios suggest that Sr isotopes in the weathering covers within the studied area are derived mainly from parent rock weathering and that the contributions from allothogenic Sr isotopes are limited. A comparison of Sr isotopic composition signatures in the weathering covers of the studied area and Guizhou Province provided insight into the Sr isotopic source and paleogeographic evolution of southern China. From the Permian to the Triassic, the continental fragment sources of the South China sedimentary basin changed significantly. In the Permian, Southern China presented the

  16. Strontium isotopes reveal weathering processes in lateritic covers in southern China with implications for paleogeographic reconstructions.

    Directory of Open Access Journals (Sweden)

    Xiao Wei

    Full Text Available The isotope ratios of Sr are useful tracers for studying parent material sources, weathering processes, and biogeochemical cycling. Mineralogical and geochemical investigations of two lateritic weathering covers, in an area close to the Tropic of Cancer (Guangxi Province, southern China, were undertaken to study the regional weathering processes and Sr isotopic sources. We found that weathering and decomposition of Rb- and Sr-bearing minerals change the Sr isotopic composition in weathering products (lateritic soils. Weathering of illite lowered the 87Sr/86Sr ratio whereas dissolving and leaching of carbonate minerals increased the 87Sr/86Sr ratio. An Fe nodular horizon is widely developed on the top of the weathering covers in the studied area and it differs from the lateritic soil horizon in mineral composition, construction, and elemental concentration. Furthermore, both Fe2O3 and P2O5 (concentrations are negatively correlated with the 87Sr/86Sr ratios, suggesting fixation of apatite by Fe oxides is a controlling factor of the Sr isotopic composition in the Fe nodular horizon. The 87Sr/86Sr and Nb/Sr ratios imply the contents and proportions of Fe nodules and clay are critical in controlling the changes of Sr isotopic composition in the Fe nodular horizon. The two stages of the weathering process of carbonate rocks are revealed by the87Sr/86Sr versus Nb/Sr diagram. The 87Sr/86Sr and Rb/Sr ratios suggest that Sr isotopes in the weathering covers within the studied area are derived mainly from parent rock weathering and that the contributions from allothogenic Sr isotopes are limited. A comparison of Sr isotopic composition signatures in the weathering covers of the studied area and Guizhou Province provided insight into the Sr isotopic source and paleogeographic evolution of southern China. From the Permian to the Triassic, the continental fragment sources of the South China sedimentary basin changed significantly. In the Permian, Southern

  17. Isotopic dependence of photoneutron cross sections around Strontium (Z=38) and Cesium (Z=55) nuclei

    International Nuclear Information System (INIS)

    Nakamura, T.; Uno, Y.; Yamadera, A.; Kase, T.

    1992-01-01

    We measured the average cross sections of (γ,n) reactions for 84 Sr, 86 Sr, 88 Sr, 85 Rb, 87 Rb, 98 Ru and 104 Ru isotopes in giant resonance region (9 to 25 MeV) using Bremsstrahlung radiation of 60 MeV maximum energy. We investigated the isotopic dependence of the average (γ,n) cross sections in giant resonance region from our experimental data and those estimated from other experimental data for Ge, Se, Zr, Mo, Sn, Te, Ce, Nd and Sm isotopes. As a result, we found that the average cross section data become highest for nuclei of neutron magic number of N = 50 and 82 except for Mo nucleus

  18. Strontium and argon isotopes in naturally weathered biotites, muscovites and feldspars

    International Nuclear Information System (INIS)

    Clauer, N.

    1981-01-01

    A Rb-Sr and K-Ar isotopical study on progressively weathered biotites, muscovites and feldspars from plutonic and eruptive rocks shows that their continental weathering is a complex phenomenon controlled by environmental conditions. During weathering of biotites, the K-Ar couple often mimics the Rb-Sr couple. The radiogenic Sr and Ar isotopes are systematically leached out, but the behaviour of the elemental Rb, K, Sr and Ar depends upon the environment. In contrast, the Sr and Ar balances of muscovites are maintained, even during very intensive weathering. In mixtures of feldspars, the common Sr seems to be leached out preferentially to the radiogenic isotope, while the K-Ar balance is maintained. (Auth.)

  19. Effects of diagenesis on strontium, carbon, nitrogen and oxygen concentration and isotopic composition of bone

    Science.gov (United States)

    Nelson, Bruce K.; Deniro, Michael J.; Schoeninger, Margaret J.; De Paolo, Donald J.; Hare, P. E.

    1986-09-01

    Paleodietary analysis based on variations in the trace element and stable isotopic composition of inorganic and organic phases in fossil bone depends on the assumption that measured values reflect in vivo values. To test for postmortem alteration, we measured 87Sr /86Sr , 13C /12C , 18O /16O and 15N /14N ratios and Sr concentrations in modern and prehistoric (610 to 5470 yr old) bones of animals with marine or terrestrial diets from Greenland. Bones from modern terrestrial feeders have substantially lower Sr concentrations and more radiogenic 87Sr /86Sr ratios than those from modern marine feeders. This contrast was not preserved in the prehistoric samples, which showed almost complete overlap for both Sr concentration and isotopic composition in bones from the two types of animals. Leaching experiments, X-ray diffraction analysis and infrared spectroscopy indicate that alteration of the Sr concentration and isotopic composition in prehistoric bone probably results from nearly complete exchange with groundwater. Oxygen isotope ratios in fossil apatite carbonate also failed to preserve the original discrimination between modern terrestrial and marine feeders. The C isotope ratio of apatite carbonate did not discriminate between animals with marine or terrestrial diets in the modern samples. Even so, the ranges of apatite δ 13C values in prehistoric bone are more scattered than in modern samples for both groups, suggesting alteration had occurred. δ 13C and δ 15N values of collagen in modern bone are distinctly different for the two feeding types, and this distinction is preserved in most of the prehistoric samples. Our results suggest that postmortem alteration of dietary tracers in the inorganic phases of bone may be a problem at all archaeological sites and must be evaluated in each case. While collagen analyzed in this study was resistant to alteration, evaluation of the possibility of diagenetic alteration of its isotopic composition in bones from other

  20. Clay mineralogy, strontium and neodymium isotope ratios in the sediments of two High Arctic catchments (Svalbard)

    Science.gov (United States)

    Hindshaw, Ruth S.; Tosca, Nicholas J.; Piotrowski, Alexander M.; Tipper, Edward T.

    2018-03-01

    The identification of sediment sources to the ocean is a prerequisite to using marine sediment cores to extract information on past climate and ocean circulation. Sr and Nd isotopes are classical tools with which to trace source provenance. Despite considerable interest in the Arctic Ocean, the circum-Arctic source regions are poorly characterised in terms of their Sr and Nd isotopic compositions. In this study we present Sr and Nd isotope data from the Paleogene Central Basin sediments of Svalbard, including the first published data of stream suspended sediments from Svalbard. The stream suspended sediments exhibit considerable isotopic variation (ɛNd = -20.6 to -13.4; 87Sr / 86Sr = 0.73421 to 0.74704) which can be related to the depositional history of the sedimentary formations from which they are derived. In combination with analysis of the clay mineralogy of catchment rocks and sediments, we suggest that the Central Basin sedimentary rocks were derived from two sources. One source is Proterozoic sediments derived from Greenlandic basement rocks which are rich in illite and have high 87Sr / 86Sr and low ɛNd values. The second source is Carboniferous to Jurassic sediments derived from Siberian basalts which are rich in smectite and have low 87Sr / 86Sr and high ɛNd values. Due to a change in depositional conditions throughout the Paleogene (from deep sea to continental) the relative proportions of these two sources vary in the Central Basin formations. The modern stream suspended sediment isotopic composition is then controlled by modern processes, in particular glaciation, which determines the present-day exposure of the formations and therefore the relative contribution of each formation to the stream suspended sediment load. This study demonstrates that the Nd isotopic composition of stream suspended sediments exhibits seasonal variation, which likely mirrors longer-term hydrological changes, with implications for source provenance studies based on fixed

  1. Human mobility on the Brazilian coast: an analysis of strontium isotopes in archaeological human remains from Forte Marechal Luz Sambaqui

    Directory of Open Access Journals (Sweden)

    Murilo Q. R Bastos

    2011-06-01

    Full Text Available This study investigated strontium isotopes in the dental enamel of 32 human skeletons from Forte Marechal Luz sambaqui (shellmound, Santa Catarina, Brazil, aiming at identifying local and non-local individuals. The archeological site presents pot sherds in the uppermost archeological layers. Dental enamel was also examined from specimens of terrestrial fauna (87Sr/86Sr = 0. 71046 to 0. 71273 and marine fauna (87Sr/86Sr = 0. 70917. The 87Sr/86Sr isotope ratio for individuals classified as locals ranged from 0. 70905 to 0. 71064 and was closer to the isotope ratio of the seawater than to the ratio of the terrestrial fauna, indicating a strong influence of marine strontium on the inhabitants of this sambaqui. The results indicate the existence of three non-local individuals (87Sr/86Sr = 0. 70761 to 0. 70835, buried in both the level without pottery and the layer with pottery, possibly originated from the Santa Catarina Plateau, close to the municipality of Lages, or from the Curitiba Plateau. The occurrence of a slight difference between the isotope ratios of local individuals buried in the archeological layer without pottery, when compared to those in the layer with pottery, suggests a possible change in dietary patterns between these two moments in the site's occupationO presente estudo investigou isótopos de estrôncio em esmalte dentário de 32 remanescentes humanos do sambaqui do Forte Marechal Luz, Santa Catarina, Brasil, com o objetivo de identificar indivíduos locais e não-locais. O sítio arqueológico apresenta fragmentos de cerâmica em suas camadas arqueológicas mais recentes. Além das amostras humanas, foram analisadas amostras de esmalte dentário de espécimes de fauna terrestre (87Sr/86Sr = 0,71046 a 0,71273 e fauna marinha (87Sr/86Sr = 0,70917. A razão 87Sr/86Sr dos indivíduos classificados como locais variou de 0,70905 a 0,71064, sendo próxima a razão de estrôncio existente nos oceanos e distante da razão obtida para a

  2. Use of strontium isotopes to identify buried water main leakage into groundwater in a highly urbanized coastal area.

    Science.gov (United States)

    Leung, Chi-Man; Jiao, Jiu Jimmy

    2006-11-01

    Previous studies indicate that the local aquifer systems in the Mid-Levels, a highly urbanized coastal area in Hong Kong, have commonly been affected by leakage from water mains. The identification of leakage locations was done by conventional water quality parameters including major and trace elements. However, these parameters may lead to ambiguous results and fail to identify leakage locations especially where the leakage is from drinking water mains because the chemical composition of drinking water is similar to that of natural groundwater. In this study, natural groundwater, seepage in the developed spaces, leakage from water mains, and parent aquifer materials were measured for strontium isotope (87Sr/86Sr) compositions to explore the feasibility of using these ratios to better constrain the seepage sources. The results show that the 87Sr/86Sr ratios of natural groundwater and leakage from water mains are distinctly different and thus, they can provide additional information on the sources of seepage in developed spaces. A classification system based on the aqueous 87Sr/86Sr ratio is proposed for seepage source identification.

  3. The geographic distribution of strontium isotopes in Danish surface waters - A base for provenance studies in archaeology, hydrology and agriculture

    Energy Technology Data Exchange (ETDEWEB)

    Frei, Karin M., E-mail: kmfrei@hum.ku.dk [Danish National Research Foundation Centre for Textile Research, SAXO Institute, University of Copenhagen, Njalsgade 80, DK-2300 Copenhagen (Denmark); Frei, Robert [Institute of Geography and Geology and Nordic Center for Earth Evolution (NordCEE), University of Copenhagen, Oster Voldgade 10, DK-1350 Copenhagen (Denmark)

    2011-03-15

    Research highlights: {yields} Strontium isotope data of 192 surface waters from Denmark. {yields} Geographic baseline distribution of bio-available fractions. {yields} Applicable for provenance studies within archaeology, geology, agriculture and hydrology. {yields} Proposal of a band of strontium isotope values to characterize 'local' Danish signatures. - Abstract: In this paper Sr isotope signatures are reported for 192 surface water (lakes/ponds and rivers/creeks) samples from within Denmark and an isotope distribution map is presented that may serve as a base for provenance applications, including archaeological migration studies, ground water - surface water - seawater interaction/contamination monitoring, and potentially for agricultural applications, including cases of authenticity proof for particular food products. The Sr isotopic compositions of surface waters range from {sup 87}Sr/{sup 86}Sr = 0.7078 to 0.7125 (average 0.7096 {+-} 0.0016; 2{sigma}). This average value lies above the range of {sup 87}Sr/{sup 86}Sr values between 0.7078 and 0.7082 expected from Late Cretaceous to Early Tertiary (Oligocene) limestones which form the dominant bedrock type in a NW-SE trending belt in Denmark. The elevated {sup 87}Sr/{sup 86}Sr signatures >{approx}0.7095 are explained by additions to the surface waters of radiogenic Sr predominantly derived from the near-surface weathering and wash-out of Quarternary glaciogenic tills and soils deposited and formed during and after the last two ice age stages (Saale and Weichsel). The Sr isotopic compositions and concentrations of the surface waters can, therefore, best be modeled by a two-component mixing involving carbonaceous bedrock and glaciogenic cover sediments as the two predominant Sr sources. A feasibility study for using Sr isotopic compositions of surface waters as a proxy for bio-available Sr signatures was conducted in a representative test area on Zealand (Land of Legends, Lejre) where there is no use

  4. The spatial patterns of water management practices are reflected in the strontium isotope ratios of human hair

    Science.gov (United States)

    Tipple, B. J.; Valenzuela, L. O.; Ehleringer, J.

    2012-12-01

    Element concentrations and isotopes of human tissues are commonly used to understand how emissions and processes within urban ecosystems affect health. Thus, it is important to understand how these elements are incorporated and flow through the urban environment and are ultimately incorporated into human tissues. Here, we designed an experiment to identify the relative importance of strontium (Sr) sources (bedrock, dust, food, and water) to hair Sr isotope ratios (87Sr/86Sr). To understand the contribution of Sr to human hair, we collected hair from individuals living in Salt Lake City, Utah. In addition to sample location, we compiled information regarding age, sex, ethnicity, and dietary habits. We found a significant association between 87Sr/86Sr value of hair and collection location. There were no significant relationships between 87Sr/86Sr value of hair and age, ethnicity, or sex. We had not predicted a relationship between 87Sr/86Sr values and collection location, because of the close proximities of sites to one another (all within an 8-km radius). We found that tap water 87Sr/86Sr values across the Salt Lake Valley varied with water management practice and this variation corresponded to hair 87Sr/86Sr value. These data suggest an additional geographically controlled source of Sr may be an important contributor to the 87Sr/86Sr value of hair. These findings suggest that local water is an important source of Sr in human hair and that hair is a sensitive temporal carrier of this environmental information. These observations have important implications to future studies of humans with regard to urban ecology, human health, forensic sciences, and anthropology.

  5. Time-series analysis of ion and isotope geochemistry of selected springs of the Nevada Test Site, Nye County, Nevada

    Energy Technology Data Exchange (ETDEWEB)

    Lyles, B.F.; Edkins, J.; Jacobson, R.L.; Hess, J.W.

    1990-11-01

    The temporal variations of ion and isotope geochemistry were observed at six selected springs on the Nevada Test Site, Nye County, Nevada and included: Cane, Whiterock, Captain Jack, Topopah, Tippipah, and Oak Springs. The sites were monitored from 1980 to 1982 and the following parameters were measured: temperature, pH, electrical conductance, discharge, cations (Ca{sup 2+}, Mg{sup 2+}. Na{sup +}, K{sup +}), anions Cl{sup {minus}}, SO{sub 4}{sup 2{minus}}. HCO{sub 3}{sup {minus}}, silica, stable isotopes ({delta}{sup 18}O, {delta}D, {delta}{sup 13}C), and radioactive isotopes ({sup 3}H, {sup 14}C). A more detailed study was continued from 1982 to 1988 at Cane and Whiterock Springs. Field microloggers were installed at these sites in 1985 to measure the high frequency response of temperature, electrical conductance, and discharge to local precipitation. Stage fluctuations near the discharge point dissolve minerals/salts as groundwater inundates the mineralized zone immediately above the equilibrium water table. This phenomena was most noticeable at Whiterock Spring and lagged the discharge response by several hours. Stable isotope analysis of precipitation and groundwater suggests a 1.5 to 2 month travel time for meteoric water to migrate from the recharge area to the discharge point. Groundwater age determinations suggest a mean age of approximately 30 years at Whiterock Spring and possibly older at Cane Spring. However, the short travel time and geochemical integrity of recharge pulses suggest that the waters are poorly mixed along the flow paths. 25 refs., 25 figs., 24 tabs.

  6. Lead and strontium isotopes as monitors of anthropogenic contaminants in the surficial environment: Chapter 12

    Science.gov (United States)

    Ayuso, Robert A.; Foley, Nora K.

    2018-01-01

    Isotopic discrimination can be an effective tool in establishing a direct link between sources of Pb contamination and the presence of anomalously high concentrations of Pb in waters, soils, and organisms. Residential wells supplying water containing up to 1600 ppb Pb to houses built on the former Mohr orchards commercial site, near Allentown, Pennsylvania, United States, were evaluated to discern anthropogenic from geogenic sources. Pb and Sr isotopic data and REE data were determined for waters from residential wells, test wells (drilled for this study), and surface waters from pond and creeks. Local soils, sediments, bedrock, Zn-Pb mineralization and coal were also analyzed, together with locally used Pb-As pesticide. Pb isotope data for residential wells, test wells, and surface waters show substantial overlap with Pb data reflecting anthropogenic actions (e.g., burning fossil fuels, industrial and urban processing activities). Limited contributions of Pb from bedrock, soils, and pesticides are evident. High Pb concentrations in the residential waters are likely related to Pb in groundwater accumulating in sediment in the residential water tanks. The Pb isotope features of waters in underlying shallow aquifers that supply residential wells in the region are best interpreted as reflecting a legacy of anthropogenic Pb rather than geogenic Pb.

  7. Strontium isotopes reveal distant sources of architectural timber in Chaco Canyon, New Mexico.

    Science.gov (United States)

    English, N B; Betancourt, J L; Dean, J S; Quade, J

    2001-10-09

    Between A.D. 900 and 1150, more than 200,000 conifer trees were used to build the prehistoric great houses of Chaco Canyon, New Mexico, in what is now a treeless landscape. More than one-fifth of these timbers were spruce (Picea) or fir (Abies) that were hand-carried from isolated mountaintops 75-100 km away. Because strontium from local dust, water, and underlying bedrock is incorporated by trees, specific logging sites can be identified by comparing (87)Sr/(86)Sr ratios in construction beams from different ruins and building periods to ratios in living trees from the surrounding mountains. (87)Sr/(86)Sr ratios show that the beams came from both the Chuska and San Mateo (Mount Taylor) mountains, but not from the San Pedro Mountains, which are equally close. Incorporation of logs from two sources in the same room, great house, and year suggest stockpiling and intercommunity collaboration at Chaco Canyon. The use of trees from both the Chuska and San Mateo mountains, but not from the San Pedro Mountains, as early as A.D. 974 suggests that selection of timber sources was driven more by regional socioeconomic ties than by a simple model of resource depletion with distance and time.

  8. Dissolution of barite for the analysis of strontium isotopes and other chemical and isotopic variations using aqueous sodium carbonate

    Science.gov (United States)

    Breit, G.N.; Simmons, E.C.; Goldhaber, M.B.

    1985-01-01

    A simple procedure for preparing barite samples for chemical and isotopic analysis is described. Sulfate ion, in barite, in the presence of high concentrations of aqueous sodium carbonate, is replaced by carbonate. This replacement forms insoluble carbonates with the cations commonly in barite: Ba, Sr, Ca and Pb. Sulfate is released into the solution by the carbonate replacement and is separated by filtration. The aqueous sulfate can then be reprecipitated for analysis of the sulfur and oxygen isotopes. The cations in the carbonate phase can be dissolved by acidifying the solid residue. Sr can be separated from the solution for Sr isotope analysis by ion-exchange chromatography. The sodium carbonate used contains amounts of Sr which will affect almost all barite 87Sr 86Sr ratios by less than 0.00001 at 1.95?? of the mean. The procedure is preferred over other techniques used for preparing barite samples for the determination of 87Sr 86Sr ratios because it is simple, rapid and enables simultaneous determination of many compositional parameters on the same material. ?? 1985.

  9. Calcium isotope fractionation between aqueous compounds relevant to low-temperature geochemistry, biology and medicine

    Science.gov (United States)

    Moynier, Frédéric; Fujii, Toshiyuki

    2017-03-01

    Stable Ca isotopes are fractionated between bones, urine and blood of animals and between soils, roots and leaves of plants by >1000 ppm for the 44Ca/40Ca ratio. These isotopic variations have important implications to understand Ca transport and fluxes in living organisms; however, the mechanisms of isotopic fractionation are unclear. Here we present ab initio calculations for the isotopic fractionation between various aqueous species of Ca and show that this fractionation can be up to 3000 ppm. We show that the Ca isotopic fractionation between soil solutions and plant roots can be explained by the difference of isotopic fractionation between the different first shell hydration degree of Ca2+ and that the isotopic fractionation between roots and leaves is controlled by the precipitation of Ca-oxalates. The isotopic fractionation between blood and urine is due to the complexation of heavy Ca with citrate and oxalates in urine. Calculations are presented for additional Ca species that may be useful to interpret future Ca isotopic measurements.

  10. Rubidium-strontium method

    International Nuclear Information System (INIS)

    Dubansky, A.

    1980-01-01

    The rubidium-strontium geological dating method is based on the determination of the Rb and Sr isotope ratio in rocks, mainly using mass spectrometry. The method is only practical for silicate minerals and rocks, potassium feldspars and slates. Also described is the rubidium-strontium isochrone method. This, however, requires a significant amount of experimental data and an analysis of large quantities of samples, often of the order of tons. The results are tabulated of rubidium-strontium dating of geological formations in the Czech Socialist Republic. (M.S.)

  11. Strontium Isotopes in Pore Water as an Indicator of Water Flux at the Proposed High-Level Radioactive Waste Repository, Yucca Mountain, Nevada

    International Nuclear Information System (INIS)

    Marshall, B.; Futa, K.

    2004-01-01

    The proposed high-level radioactive waste repository at Yucca Mountain, Nevada, would be constructed in the high-silica rhyolite (Tptp) member of the Miocene-age Topopah Spring Tuff, a mostly welded ash-flow tuff in the ∼500-m-thick unsaturated zone. Strontium isotope compositions have been measured in pore water centrifuged from preserved core samples and in leachates of pore-water salts from dried core samples, both from boreholes in the Tptp. Strontium isotope ratios ( 87 Sr/ 86 Sr) vary systematically with depth in the surface-based boreholes. Ratios in pore water near the surface (0.7114 to 0.7124) reflect the range of ratios in soil carbonate (0.7112 to 0.7125) collected near the boreholes, but ratios in the Tptp (0.7122 to 0.7127) at depths of 150 to 370 m have a narrower range and are more radiogenic due to interaction with the volcanic rocks (primarily non-welded tuffs) above the Tptp. An advection-reaction model relates the rate of strontium dissolution from the rocks with flow velocity. The model results agree with the low transport velocity (∼2 cm per year) calculated from carbon-14 data by I.C. Yang (2002, App. Geochem., v. 17, no. 6, p. 807-817). Strontium isotope ratios in pore water from Tptp samples from horizontal boreholes collared in tunnels at the proposed repository horizon have a similar range (0.7121 to 0.7127), also indicating a low transport velocity. Strontium isotope compositions of pore water below the proposed repository in core samples from boreholes drilled vertically downward from tunnel floors are more varied, ranging from 0.7112 to 0.7127. The lower ratios ( 87 Sr/ 86 Sr of 0.7115. Ratios lower than 0.7115 likely reflect interaction of construction water with concrete in the tunnel inverts, which had an 87 Sr/ 86 Sr < 0.709. These low Sr ratios indicate penetration of construction water to depths of ∼20 m below the tunnels within three years after construction, a transport velocity of ∼7 m per year. These studies show that

  12. Geofluids Assessment of the Ayub and Shafa Hot Springs in Kopet-Dagh Zone (NE Iran: An Isotopic Geochemistry Approach

    Directory of Open Access Journals (Sweden)

    Hossein Mohammadzadeh

    2017-01-01

    Full Text Available Geothermal energy has a wide range of uses in our life. It is very important to characterize the temperature and the depth of geothermal reservoirs. The aim of this paper is the determination of type, origin source of water temperature, and depth of water circulation in the Ayub-Peighambar and Shafa (AP and SH hot springs, located in NE Iran, using hydrogeochemistry and environmental isotopes (2H and 18O. AP hot spring has elevated temperature (36–40°C and as such is very important for balneotherapy and geotourism industry purposes. The average values of δ18O and δ2H for this hot spring (−10‰ and −73‰, resp. are analogous to that of geothermal and meteoric waters. This indicates that the heat source cannot be related to volcanic activities (with average δ18O value of about 5‰ and it is most probably associated with geothermal gradient with deep circulation of groundwater through faults. Based on Na-K geothermometers coupled with isotopic (18O and 2H geochemistry the temperature of the AP geothermal reservoir was estimated to be in the range of 100–150°C with 3–5 and 4.2 kilometres’ depth, respectively. Chemically, the AP samples are CaSO4 facies with a chemically homogeneous source and steam heated waters type.

  13. Using isotope geochemistry to discuss the role of crust-mantle interaction in the formation of endogenetic mega-deposits

    International Nuclear Information System (INIS)

    Zhang Lisheng

    2005-01-01

    Isotope characteristics of some mega-deposits from literature and new results on twenty deposits (ten of them are mega-deposits) show that there exists traces of crust-mantle interaction. It has been established that the interaction all took place in the mantle under many situations. The theory of isotope geochemistry on the genesis of mega-deposits has been discussed. According to the theory, these deposits are a kind of special phenomena, but they have a common factor, i.e. mantle metasomatism produced by the crust-mantle interaction in the mantle no matter what the ore-forming elements diversity may be. The granites with great accumulation of uncompatible elements can be considered as the analogues of mega-deposits. According to the statistical results, it is possible that they formed at a period before about 2 Ga during which the recycling of the materials was accompanied with the obvious crust-mantle interaction and can produce the volatile components which are poor in the mantle. (authors)

  14. Sulfur and lead isotope geochemistry of the orogenic gold deposits in the eastern Kunlun area, Qinghai province

    International Nuclear Information System (INIS)

    Feng Chengyou; Zhang Dequan; Li Daxin; She Hongquan; Zhu Huaping

    2003-01-01

    Based on researches on the basic geological characteristics and sulfur and lead isotopic geochemistry of four typical gold deposits, it is considered that they have many similar geo-geochemical characteristics and are all related genetically to orogenic process. Therefore, they should belong to a type of orogenic gold deposits according to the newest classification of gold deposits provided by Kerrich et al. (2000). There is a big change in the average 34 S values of the sulfides selected from different deposits, varying from -3.7‰-4.4‰ and tower-shape distribution is apparent. The lead isotope in four gold deposits is characterized by high compositions and minor changes, with 206 Pb/ 204 Pb > 18.3380, 207 Pb/ 204 Pb > 15.5555, 208 Pb/ 204 Pb >38.1796 in ores and wall-rocks, it can be concluded that the ore-forming material consisting of sulfur and lead are mainly derived from wall-rocks. Intensive subduction and collision during late Paleozoic and early Mesozoic not only formed deep faults, large-scale shear belt, and low-order folds and faults but also induced fluidization and mineralization, and resulted in formation and zonal distribution of several large or medium gold deposits in this area. (authors)

  15. Neodymium and strontium isotope study of ophiolite and orogenic lherzolite petrogenesis

    International Nuclear Information System (INIS)

    Richard, P.; Allegre, C.J.; Paris-7 Univ., 75

    1980-01-01

    Neodymium isotopic analyses have been measured on nine ophiolites and four orogenic lherzolites. Epsilonsub(Nd) varies from +12 to +3 in the ophiolites and from +18 to +2 in the orogenic lherzolites. The majority of the analyses plot on a epsilonsub(Nd)-epsilonsub(Sr) correlation line as defined by Nd and Sr isotopic analyses of oceanic basalts. However, certain ophiolitic and lherzolitic samples exhibit high 87 Sr/ 86 Sr ratios and as such lie to the right of the correlation line towards seawater compositions. From these data one can postulate several origins for ophiolites including that of mid-ocean ridges and ocean islands. If the orogenic lherzolites are interpreted as representative of the mantle occurring below active ridges a more complex model is required involving mantle heterogeneity and multi-episodic chemical fractionation starting prior to 2 Ga ago. (orig.)

  16. Strontium isotope data for recent andesites in Ecuador and North Chile

    International Nuclear Information System (INIS)

    Francis, P.W.; Thorpe, R.S.; Moorbath, S.

    1977-01-01

    New Sr isotope data are presented for andesite lavas from active volcanoes in Ecuador and North Chile. Twenty-three samples from five Ecuadorian volcanoes have 87 Sr/ 86 Sr ratios most of which are essentially within analytical error, and average 0.7044. In contrast, 16 samples from the San Pedro-San Pablo volcano complex in North Chile have 87 Sr/ 86 Sr ratios between 0.7058 and 0.7072. These samples show no correlation between 87 Sr/ 86 Sr and 87 Rb/ 86 Sr, nor between 87 Sr/ 86 Sr and other elements or ratios. The major difference in setting between the two volcanic provinces lies in the thickness of the continental crust; 40-50 km beneath Ecuador, 70 km beneath North Chile. Andesites from both areas are derived primarily from the mantle, but those from North Chile show evidence of a significant Sr isotopic contribution from the continental crust. (Auth.)

  17. Copper isotope fractionation between aqueous compounds relevant to low temperature geochemistry and biology

    Science.gov (United States)

    Fujii, Toshiyuki; Moynier, Frédéric; Abe, Minori; Nemoto, Keisuke; Albarède, Francis

    2013-06-01

    Isotope fractionation between the common Cu species present in solution (Cu+, Cu2+, hydroxide, chloride, sulfide, carbonate, oxalate, and ascorbate) has been investigated using both ab initio methods and experimental solvent extraction techniques. In order to establish unambiguously the existence of equilibrium isotope fractionation (as opposed to kinetic isotope fractionation), we first performed laboratory-scale liquid-liquid distribution experiments. Upon exchange between HCl medium and a macrocyclic complex, the 65Cu/63Cu ratio fractionated by -1.06‰ to -0.39‰. The acidity dependence of the fractionation was appropriately explained by ligand exchange reactions between hydrated H2O and Cl- via intramolecular vibrations. The magnitude of the Cu isotope fractionation among important Cu ligands was also estimated by ab initio methods. The magnitude of the nuclear field shift effect to the Cu isotope fractionation represents only ˜3% of the mass-dependent fractionation. The theoretical estimation was expanded to chlorides, hydroxides, sulfides, sulfates, and carbonates under different conditions of pH. Copper isotope fractionation of up to 2‰ is expected for different forms of Cu present in seawater and for different sediments (carbonates, hydroxides, and sulfides). We found that Cu in dissolved carbonates and sulfates is isotopically much heavier (+0.6‰) than free Cu. Isotope fractionation of Cu in hydroxide is minimal. The relevance of these new results to the understanding of metabolic processes was also discussed. Copper is an essential element used by a large number of proteins for electron transfer. Further theoretical estimates of δ65Cu in hydrated Cu(I) and Cu(II) ions, Cu(II) ascorbates, and Cu(II) oxalate predict Cu isotope fractionation during the breakdown of ascorbate into oxalate and account for the isotopically heavy Cu found in animal kidneys.

  18. An isotopic and fluid inclusion study of fracture calcite from borehole OL-KR1 at the Olkiluoto site, Finland

    International Nuclear Information System (INIS)

    Blyth, A.; Frape, S.; Blomqvist, R.; Nissinen, P.; McNutt, R.

    1998-04-01

    A study of the geochemistry of fracture filling calcite in borehole OL-KR1 at the radioactive waste disposal investigation site Olkiluoto (in Finland) was undertaken in 1998. The purpose of the present study is to characterize the fracture calcite using mineralogy, oxygen, carbon and strontium isotopes, and fluid inclusions in order to determine past and present chemical and isotopic condition at the site

  19. An isotopic and fluid inclusion study of fracture calcite from borehole OL-KR1 at the Olkiluoto site, Finland

    Energy Technology Data Exchange (ETDEWEB)

    Blyth, A.; Frape, S. [Univ. of Waterloo, ON (Canada); Blomqvist, R.; Nissinen, P. [Geological Survey of Finland, Espoo (Finland); McNutt, R. [McMaster Univ. of Hamilton, ON (Canada)

    1998-04-01

    A study of the geochemistry of fracture filling calcite in borehole OL-KR1 at the radioactive waste disposal investigation site Olkiluoto (in Finland) was undertaken in 1998. The purpose of the present study is to characterize the fracture calcite using mineralogy, oxygen, carbon and strontium isotopes, and fluid inclusions in order to determine past and present chemical and isotopic condition at the site 39 refs.

  20. Isotopic Geochemistry Applied on Mortars of the Katholikon of the Monastery of Timios Prodromos in the Prefecture of Serres, Greece

    Science.gov (United States)

    Dotsika, Elissavet; Iliadis, Efstathios; Kyropoulou, Daphne; Karalis, Petros

    2017-12-01

    The Monastery of Timios Prodromos is the most important Byzantine monument in the prefecture of Serres and one of the most important monastic foundations of Byzantine times in Northern Greece. It was founded in the late 13th century from Ioannikios and then renovated by his nephew, Joachim. The catholic dates back to the 14th century, and specifically between 1300-1333, under the rule of the second founder Joachim. Considering the pathology of Byzantine mural, for the most effective work on removal of over-paintings layer, fixing, restoration, recovery and maintenance of the painted surface and the substrate, it was decided the sampling from exact points of the mural painting representing the different phases, in order to determine their composition, the technology of construction materials, corrosion mechanisms and the proposal for restoration methodology. The methods to be used require very small quantities of material. The measurements are considered almost non-destructive and based on isotopic geochemistry. The techniques used are X-ray diffraction (XRD), scanning electron microscopy (SEM / EDXA) and isotopic analyzes (d18O and d13C) in a mass spectrometer (IRMS). The study of the samples was carried out by scanning electron microscopy with X-ray microanalyser and analysis of stable isotopes. The study shows that apart from the calcite present in all pigment samples, straw was used as a binder. There is also a mixing of dyes to produce the desired tint while in many cases there are different colour layers. The decay in the mural is extensive, especially in the lower layers of the wall, which have been severely affected by humidity and candle smoke. The creation of gypsum on the surface of the murals is intense and evident in most of the spectra taken

  1. Studies of geothermal background and isotopic geochemistry of thermal waters in Jiangxi Province

    International Nuclear Information System (INIS)

    Zhou Wenbin; Sun Zhanxue; Li Xueli; Shi Weijun

    1996-10-01

    The terrestrial heat flow measurement, isotope and geochemical techniques have been systematically applied to the geothermal systems in Jiangxi Province. Results show that the thermal waters in the study area all belong to the low-medium temperature convective geothermal system, which essentially differs from high temperature geothermal systems with deep magmatic heat sources. It has been proven that the isotope and geochemical techniques are very useful and effective in geothermal exploration. (13 refs., 14 tabs., 8 figs.)

  2. Contribution of isotopic and geochemical tracers to the administration of water resources: the strontium case

    International Nuclear Information System (INIS)

    Verdoux, P.; Lancelot, J.; Faillat, J.P.

    1995-01-01

    A better understanding of groundwater origin(s) and a quantitative and qualitative evaluation of exploited resources is a preliminary condition for rational administration and preventive actions. The determination of Sr contents and isotopic compositions associated or not to other elements is a new method applied in underground domains which has proven to be effective for example in Languedoc-Rousillon, particularly in areas where classical natural and even artificial tracers are unreliable. The use of 87 Sr/ 86 Sr tracer is based on the condition that each analysed rock-system is defined by a typical isotopic composition. In the Cevennes and Lozere, sedimentary carbonate rocks display 87 Sr/ 86 Sr ratios ranging from 0.707 to 0.709, similar to those of seawater,while silicate rocks exhibit values from 0.710 to 0.750, depending on Rb/Sr ratios, ages and resistance of the different minerals to weathering processes. Sr data obtained in the Lozere suggest important binary mixing of water between an homogeneous end member representing the composition of water flowing on the crystalline basement and a second component corresponding to water from karstic springs and to captive waters of the lower aquifer reached at 200 m in depth by borehole. Calculated mixing curves between the basement and the karstic water end members would allow to define the nature and volumetric importance of storage and to evaluate pollution risks. (J.S.). 17 refs., 9 figs., 3 tabs

  3. Geochemistry contribution of Pb isotopes on basalts origin study from Parana basin, Brazil

    International Nuclear Information System (INIS)

    Marques, L.S.; Dupre, B.; Allegre, C.J.

    1990-01-01

    This paper presents thirty new Pb-isotope and concentration data for low- and high-tiO sub(2) continental flood basalts of the Parana Basin. The results obtained from representative samples show significant differences with respect to type and location of these basic rocks. The low- and high-TiO sub(2) basalts from the northern region of the Parana Basin exhibit very similar Pb-isotope compositions. On the other hand, the low-TiO sub(2) basalts of central and southern areas, which exhibit low Sr initial isotope ratios (less than 0,7060), show very small variation in Pb isotope compositions which are highly enriched in radiogenic Pb in comparison with the analogues of northern region. The high-TiO sub(2) basic rocks analysed from northern and central regions have the same values for Pb isotope ratios, which are slightly more radiogenic compared with high-TiO sub(2) basalts from southern region. The data obtained, combined with other geochemical (major and trace elements, including rare earths) and isotope (Sr and Nd) results support the view that the basalts from northern and southern areas of the Parana Basin originated in lithospheric mantle reservoirs with different geochemical characteristics. (author)

  4. Rb-Sr and Nd-Sr isotope geochemistry and petrogenesis of the Misho Mountains mafic dikes (NW Iran

    Directory of Open Access Journals (Sweden)

    Maryam Ahankoub

    2017-02-01

    Full Text Available Introduction There are some theories about the Paleotethys event during the Paleozoic that have been proposed by geologists (Metcalfe, 2006. Some scientist offered some pieces of evidence about the northern margin of Gondwana (Zhu et al., 2010. The Paleotethys Ocean and Hercynian orogenic report first in Iran, have been Offered from the Morrow and Misho Mountain (Eftekharnejad, 1981. Misho Mountains is located between the north and south Misho faults and cause the formation of a positive flower structure (Moayyed and Hossainzade, 2011. There is theory about Misho southern fault as the best candidate of the Paleotethys suture zone (Moayyed and Hossainzade, 2011. Geochemistry and Sr –Nd isotopic data of the A2 granitic and Synite rocks of the East Misho, indicate that the magmatism post collision has occurred in the active continental margin by extensional zones of the following the closure of the Paleotethys (Ahankoub, 2012. Granite and syenite rocks have been cut by mafic dikes. Mafic dikes are often formed in extensional tectonic settings related to mantle plume or continental break –up (Zhu et al., 2009. In this paper, we use the geochemistry and Nd-Sr isotope data to determined petrogenesis, tectono-magmatic setting and age of Misho mafic dikes. Materials and methods After petrography study of 30 thin sections of mafic dike rocks, 8 samples were selected for whole-rock chemical analyses using ICP-MS and ICP-AES instruments by ACME Company in Vancouver, Canada. We prepared 6 sample For Sm-Nd and Rb-Sr analysis. Sr and Nd isotope ratios were measured with a thermal ionization mass spectrometer, VG Sector 54–30 at the Nagoya University. The isotope abundances of Rb, Sr, Nd, and Sm were measured by the ID method with a Finnigan MAT Thermoquad THQ thermal ionization quadrupole mass spectrometer at the Nagoya University. NBS987 and JNdi-1 were measured as natural Sr and Nd isotope ratio standards (Tanaka et al., 2000. Averages and 2σ errors

  5. Isotope geochemistry of xenoliths from East Africa. Implications for development of mantle reservoirs and their interaction

    Energy Technology Data Exchange (ETDEWEB)

    Cohen, R S; O' Nions, R K [Cambridge Univ. (UK). Dept. of Earth Sciences; Dawson, J B [Sheffield Univ. (UK). Dept. of Geology

    1984-05-01

    Pd, Nd and Sr isotope analyses together with U, Pb, Sm, Nd, Rb and Sr concentrations have been obtained for separated phases of lherzolite and bulk rock mafic granulite xenoliths in Recent volcanics from Tanzania. A garnet lherzolite from the Lashaine vent has yielded the least radiogenic Pb (/sup 206/Pb//sup 204/PB=15.55) and Nd (/sup 143/Nd//sup 144/Nd=0.51127; epsilon/sup 0/sub(Nd)=-26.7) isotope compositions recorded so far for an ultramafic xenolith, and /sup 87/Sr//sup 86/Sr=0.83604. The Pb isotope compositions of the mafic granulites are variable 15.77isotope results suggest that the mantle part of the continental lithosphere beneath Tanzania has components that have undergone a complex history that includes major chemical fractionations ca. 2.0 Ga ago. A phlogopite-amphibole vein from the Pello Hill sample has Sr, Nd and Pb isotope compositions similar to those of mid-ocean ridge basalts, indicating both a young emplacement age for the vein material and a source which had an isotopic signature characteristic of depleted mantle. The Sr, Nd and Pb isotope systematics of ultramafic xenoliths do not conform with those of MORB, particularly in terms of their Pb-Sr, and Nd-Pb relationship. In this regard they are similar to some ocean islands and could be a viable source material for some ocean island basalts at least. The mantle part of the continental lithosphere is as likely to contain recycled components derived from the continental crust as are other regions of mantle. If the mantle part of continental lithosphere is invoked as a source for ocean islands, it does not negate the possibility that substantial recycled components are involved.

  6. Variation of lithium isotope geochemistry during basalt weathering and secondary mineral transformations in Hawaii

    Science.gov (United States)

    Ryu, Jong-Sik; Vigier, Nathalie; Lee, Sin-Woo; Lee, Kwang-Sik; Chadwick, Oliver A.

    2014-11-01

    Lithium isotopes are a potential tracer of silicate weathering but the relationship between lithium isotope compositions and weathering state still need to be established with precision. Here, we report Li concentrations and Li isotope compositions of soils developed along a 4 million year humid-environment chronosequence in the Hawaiian Islands. Li concentrations are variable with depth and age, ranging from 0.24 to 21.3 ppm, and significant Li depletions (up to 92%) relative to parent basalts are systematically enhanced towards the surface. Our calculations show that the relative contribution from atmospheric deposits to the Li soil budget remains small, with a maximum contribution from dust Li of 20% at the oldest site. This is explained by the capacity of the weathering products to retain, within the profiles, the Li coming from basalt alteration, and allows us to explore more specifically the role of alteration processes on soil Li isotope signatures. The δ7Li values display a large range between -2.5‰ and +13.9‰. The youngest soils (0.3 ka) display the same δ7Li value as fresh basalt, regardless of depth, despite ∼30% Li loss by leaching, indicating that there is little Li isotope fractionation during the incipient stage of weathering. δ7Li values for the older soils (⩾20 ka) vary non-linearly as a function of time and can be explained by progressive mineral transformations starting with the synthesis of metastable short-range order (nano-crystalline) minerals and followed by their transformation into relatively inert secondary minerals. Results highlight significant Li isotope fractionation during secondary mineral formation and in particular during Li uptake by kaolinite. Finally, we suggest that the non-monotonous evolution of the regolith δ7Li value over the last 4 Ma is consistent with climatic variations, where congruent release of Li isotopes occurs during warmer periods.

  7. Environmental controls on the boron and strontium isotopic composition of aragonite shell material of cultured Arctica islandica

    Directory of Open Access Journals (Sweden)

    Y.-W. Liu

    2015-06-01

    Full Text Available Ocean acidification, the decrease in ocean pH associated with increasing atmospheric CO2, is likely to impact marine organisms, particularly those that produce carbonate skeletons or shells. Therefore, it is important to investigate how environmental factors (seawater pH, temperature and salinity influence the chemical compositions in biogenic carbonates. In this study we report the first high-resolution strontium (87Sr / 86Sr and δ88 / 86Sr and boron (δ11B isotopic values in the aragonite shell of cultured Arctica islandica (A. islandica. The 87Sr / 86Sr ratios from both tank water and shell samples show ratios nearly identical to the open ocean, which suggests that the shell material reflects ambient ocean chemistry without terrestrial influence. The 84Sr–87Sr double-spike-resolved shell δ88 / 86Sr and Sr concentration data show no resolvable change throughout the culture period and reflect no theoretical kinetic mass fractionation throughout the experiment despite a temperature change of more than 15 °C. The δ11B records from the experiment show at least a 5‰ increase through the 29-week culture season (January 2010–August 2010, with low values from the beginning to week 19 and higher values thereafter. The larger range in δ11B in this experiment compared to predictions based on other carbonate organisms (2–3‰ suggests that a species-specific fractionation factor may be required. A significant correlation between the ΔpH (pHshell − pHsw and seawater pH (pHsw was observed (R2 = 0.35, where the pHshell is the calcification pH of the shell calculated from boron isotopic composition. This negative correlation suggests that A. islandica partly regulates the pH of the extrapallial fluid. However, this proposed mechanism only explains approximately 35% of the variance in the δ11B data. Instead, a rapid rise in δ11B of the shell material after week 19, during the summer, suggests that the boron uptake changes when a thermal

  8. Groundwater geochemistry of nile delta-desert interface 1.isotope hydrology

    International Nuclear Information System (INIS)

    Hussein, M.F.; Nada, A.A.; Awad, M.A.

    1995-01-01

    Sustenance and environmental protection of groundwater supply is of major concern in the integral environmental development in the arid to sub-arid regions in the Nile basin. Isotope data ( 18O , 2H and 3H ) of groundwater in the west of the Nile delta indicates the contribution of palaeo groundwater component (in the range 0.1 - 0.8 with means of 0.39 and 0.52 for tahrir and khatatbah, respectively) along with sub recent recharge from the delta aquifer and recent recharge from irrigation conveyance canals in desert. Isotope mixing model (developed as Two-input table using excel TM spreads heat on apple Macintosh TM) is proposed to explain the apparent discrepancies in groundwater isotopic composition of khatatbah and tahrir areas assuming the contribution of two isotopically different palaeo-oples with two isotopically similar maind delta groundwater poles. About 0.30% 1 8 O depletion per 10 Km downstream is detected and low northward groundwater recharge is suggested along 75 Km of the western strip of rosetta Nile. Higher sub-recent recharge from the main delta aquifer is believed to take place in khatatbah than tahrir whereas the last is believed to be replenished at present from the irrigation/ drainage network and irrigated fields with higher pollution risk for groundwater system in tahrir aquifer is exposed to northern marine intrusion. Lowering of the piezo metric level is to be expected in the newly exploited desertic areas under over pumping. 9 figs

  9. GEOCHEMISTRY AND ISOTOPE HYDROLOGY OF AN URBAN AQUIFER, SUBTROPICAL AFRICA, CENTRAL AFRICAN REPUBLIC

    International Nuclear Information System (INIS)

    HUSSEIN, M.F.; ISLAM, A.; GAMAL, S.; GAETAN, M.; DJEBEBE, C.

    2008-01-01

    Africa south of the Great Sahara has abundant water resources, however, its aquifers are seldom studied and/or inadequately managed. This study presents a geochemical and isotope hydrology study on the aquifer of Bangui city, the capital of the Central African Republic (RCA), on the northern borders of Congo with RCA.The obtained chemical data demonstrated the role of biogenic CO 2 gas, solid phases and cation exchange in the hydrochemistry of the studied groundwater. The conjunctive use of the major dissolved constituents and the isotope contents ( 18 O and 2 H) showed that the alteration of primary silicates and the dissolution of carbonates are the predominant processes that locally define the zones of dilute and relatively charged groundwater, respectively.The isotope data illustrated that evaporation is non-significantly contributing to the water loss from the aquifer, while transpiration (process that goes almost without isotopic fractionation) is prevailing in the water balance of the local drainage basin, with a significant fraction of the transpired vapour being recycled. An isotopic i nverse continental effect(eastward from Cameron to RCA) is explained through differences in air temperatures, amount and altitude of precipitation rather than by inverse movement of humid air masses westward in Central Africa

  10. The isotope geochemistry of hot springs gases and waters from Coromandel and Hauraki

    International Nuclear Information System (INIS)

    Lyon, G.L.; Giggenbach, W.F.

    1992-01-01

    Carbon, hydrogen and oxygen stable isotope analyses have been made on carbon dioxide,methane and water from warm and hot springs in the Coromandel Peninsula and Hauraki Plains. Most of the waters are isotopically unaltered meteoric waters. Methane δ 1 3C values vary widely, from -30%o to -72%o. Warm springs in swamps at Maketu and Kerepehi have microbial methane probably added to the water near the surface. Puriri, Okoroire and Miranda springs produce thermally derived methane, and the Hot Water Beach gas is similar to the Kaitoke gas in chemistry and isotopic composition but altered by shallow microbial oxidation. The Te Aroha gas, though, is not inconsistent with a geothermal origin and the boiling springs and oxygen-isotope altered water are further evidence for high temperatures. Other spring gases have mixtures of thermogenic and microbial methane and none are closely similar to major NZ geothermal CH 4 composition. CO 2 , which is usually present in lesser amounts than N 2 , has isotopic values which suggest a geothermal origin at Te Aroha and Maketu, but otherwise indicates a crustal origin. The dominance of N 2 implies that the fluid flows are tectonic fracture flow rather than geothermal. 3 He/ 4 He data gives further evidence of no major contribution from magmatic material except at Maketu, on the NW boundary of the TVZ. (author). 24 refs., 4 figs., 2 tabs

  11. 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.

  12. 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.

  13. Variation of stable silicon isotopes. Analytical developments and applications in Precambrian geochemistry

    International Nuclear Information System (INIS)

    Abraham, Kathrin

    2010-01-01

    The work presented in this thesis predominantly deals with bulk-rock measurements of silicon stable isotopes on a Multi Collector-ICP-MS. Analyses were performed in cooperation with the Royal Museum for Central Africa, Belgium. The first section describes how the first analysis of δ 30 Si on a conventional Nu PlasmaTM Multi-Collector ICP-MS instrument can be enabled by the elimination of 14N16O interference overlying the 30Si peak. The determination of δ 30 Si was rendered possible owing to new instrumental upgrades that facilitate the application of a higher mass resolution. The careful characterisation of appropriate reference materials is indispensable for the assessment of the accuracy of a measurement. The determination of U.S. Geological Survey (USGS) reference materials represents the second objective of this section. The analysis of two Hawaiian standards (BHVO-1 and BHVO-2) demonstrates precise and accurate δ 30 Si determinations and provides cross-calibration data as a quality control for other laboratories. The second section focuses on coupled silicon-oxygen isotopic evidences for the origin of silicification in mafic volcanic rocks of the Barberton Greenstone Belt, South Africa. In contrast to the modern Earth, silicification of near-surface layers, including chert formation, were widespread processes on the Precambrian ocean floor, and demonstrate the ubiquity of extreme silica mobilization in the early Earth. This section outlines the investigation of silicon and oxygen isotopes on three different stratigraphic sections of variably silicified basalts and overlying bedded cherts from the 3.54 Ga, 3.45 Ga and 3.33 Ga Theespruit, Kromberg and Hooggenoeg Formations, respectively. Silicon isotopes, oxygen isotopes and the variable SiO 2 -contents demonstrate a positive correlation with silicification intensity in all three sections, with varying gradients of δ 30 Si vs. δ 18 O arrays for different sections. Seawater has been regarded as the most

  14. Variation of stable silicon isotopes. Analytical developments and applications in Precambrian geochemistry

    Energy Technology Data Exchange (ETDEWEB)

    Abraham, Kathrin

    2010-05-28

    The work presented in this thesis predominantly deals with bulk-rock measurements of silicon stable isotopes on a Multi Collector-ICP-MS. Analyses were performed in cooperation with the Royal Museum for Central Africa, Belgium. The first section describes how the first analysis of δ{sup 30}Si on a conventional Nu PlasmaTM Multi-Collector ICP-MS instrument can be enabled by the elimination of 14N16O interference overlying the 30Si peak. The determination of δ{sup 30}Si was rendered possible owing to new instrumental upgrades that facilitate the application of a higher mass resolution. The careful characterisation of appropriate reference materials is indispensable for the assessment of the accuracy of a measurement. The determination of U.S. Geological Survey (USGS) reference materials represents the second objective of this section. The analysis of two Hawaiian standards (BHVO-1 and BHVO-2) demonstrates precise and accurate δ{sup 30}Si determinations and provides cross-calibration data as a quality control for other laboratories. The second section focuses on coupled silicon-oxygen isotopic evidences for the origin of silicification in mafic volcanic rocks of the Barberton Greenstone Belt, South Africa. In contrast to the modern Earth, silicification of near-surface layers, including chert formation, were widespread processes on the Precambrian ocean floor, and demonstrate the ubiquity of extreme silica mobilization in the early Earth. This section outlines the investigation of silicon and oxygen isotopes on three different stratigraphic sections of variably silicified basalts and overlying bedded cherts from the 3.54 Ga, 3.45 Ga and 3.33 Ga Theespruit, Kromberg and Hooggenoeg Formations, respectively. Silicon isotopes, oxygen isotopes and the variable SiO{sub 2}-contents demonstrate a positive correlation with silicification intensity in all three sections, with varying gradients of δ{sup 30}Si vs. δ{sup 18}O arrays for different sections. Seawater has been

  15. Contributions of isotopic bio-geochemistry to the analysis of water - soil - root interactions

    International Nuclear Information System (INIS)

    Cayet, S.

    2001-07-01

    The aim of this work is to study the origin of the isotopic signal of the water produced by plants transpiration. It stresses more particularly on the water movements between the soil and the plant in a context of heterogenous water availability for the root system. The use of water isotopes ( 18 O and 2 H) should allow to precise the water extraction depth of the roots and the plant strategy in front of a hydric stress of edaphic origin. The first chapter presents the place of water in the soil-plant-atmosphere continuum, the different potential sources of water accessible to the plant, the principles of water absorption and the hydric transfer in the plant in relation with the variations of water absorption and of the evaporative conditions. The isotopic method is introduced with the natural variability of the isotopic composition of the atmospheric and soil waters. Finally, the reaction of the plant in front of a hydric stress is described. The second chapter presents a series of experiments carried out in the natural environment and shows the problems encountered during the determination of water origin in heterogenous hydric availability conditions. The third chapter describes the experiments performed in controlled environment. One series of experiments is performed in homogenous hydric availability condition. The aim is to analyze the isotopic signal emitted by the plant and its significance with respect to the feeding water. The second series of experiments is performed in heterogenous hydric availability conditions and in stable or variable climatic conditions. In the last chapter, the different experiments performed in natural environment are presented, first in optimum hydric availability conditions, and second in variable hydric conditions. These experiments allow to reconstruct the isotopic signal of the soil water which is recorded by the plant and to precise the preferential areas of water extraction by the roots, and the competitive behaviour of

  16. Sr and Nd isotope geochemistry of coexisting alkaline magma series, Cantal, Massif Central, France

    International Nuclear Information System (INIS)

    Downes, H.

    1984-01-01

    Sr and Nd isotope analyses are presented for Tertiary continental alkaline volcanics from Cantal, Massif Central, France. The volcanics belong to two main magma series, silica-saturated and silica-undersaturated (with rare nephelinites). Trace element and isotopic data indicate a common source for the basic parental magmas of both major series; the nephelinites in contrast must have been derived from a mantle source which is isotopically and chemically distinct from that which gave rise to the basalts and basanites. 87 Sr/ 86 Sr initial ratios range from 0.7034 to 0.7056 in the main magma series (excluding rhyolites) and 143 Nd/ 144 Nd ratios vary between 0.512927 and 0.512669; both are correlated with increasing SiO 2 in the lavas. The data can be explained by a model of crustal contamination linked with fractional crystallisation. This indicates that crustal magma chambers are the sites of differentiation since only rarely do evolved magmas not show a crustal isotopic signature and conversely basic magmas have primitive isotopic ratios unless they contain obviuos crustal-derived xenocrysts. Potential contaminants include lower crustal granulites or partial melts of upper crustal units. Equal amounts of contamination are required for both magma series, refuting hypotheses of selective contamination of the silica-saturated series. The isotopic characteristics of the apparently primary nephelinite lavas demonstrates widespread heterogeneity in the mantle beneath Cantal. Some rhyolites, previously thought to be extremely contaminated or to be crustally derived, are shown to have undergone post-emplacement hydrothermal alteration. (orig.)

  17. Chlorine isotopic geochemistry of salt lakes in the Qaidam Basin, China

    Digital Repository Service at National Institute of Oceanography (India)

    Liu, W.G.; Xiao, Y.K.; Wang, Q.Z.; Qi, H.P.; Wang, Y.H.; Zhou, Y.M.; Shirodkar, P.V.

    *Cl+ ion. Int. J. Mass Spectrom. Ion Process., 116: crysatallization of saline minerals in salt lake. J. Salt Lake 183-192. Sci., 2: 35-40 (in Chinese). Xiao, Y.K., Sun, D.P., Wang, Y.H., Qi, H.P. and Jin, L., 1992. Boron isotopic compositions of brine..., sediments, and source water in Da Qaidam Lake, Qinghai, China. Geochim. Cos- mochim. Acta, 56: 1.561-1568. Xiao, Y.K., Jin, L., Liu. W.G., Qi, H.P., Wang, W.H. and Sun, D.P., 1994a. The isotopic compositions of chlorine in Da Qaidam Lake. Chin. Sci...

  18. Petrology and geochemistry of the marbles and calcosilicated rocks from Ipira, Bahia - Brazil

    International Nuclear Information System (INIS)

    Oliveira, M.A.F.T. de.

    1976-01-01

    This work explains a study of marbles and diopsitites from Serra das Panelas, Ipira, Bahia, Brazil. Petrographic analysis, chemistry some elements, trace elements and rare earths, isotopic analysis of Strontium, carbon and oxigen, and geochronological determinations were done. The ages founded correspond to Transamazonic Orogenetic cicle, with Archean age, confirmed by the 18 O values found, which give to marble, ages about 2.500 my. The mineralogy and the texture give to marble an invulgar aspect, making a confusion with carbonate. The petrochemical data and the geochemistry of 13 C and 18 O isotopes showed that the marble and diopsitites was formed from the old marine carbonates. The geochemistry of rare earth suggests a strong correlation with carbonitic and alkaline rocks. An hybrid origem to this rocks is proposed. (C.D.G.) [pt

  19. A Review of the Stable Isotope Bio-geochemistry of the Global Silicon Cycle and Its Associated Trace Elements

    Directory of Open Access Journals (Sweden)

    Jill N. Sutton

    2018-01-01

    Full Text Available Silicon (Si is the second most abundant element in the Earth's crust and is an important nutrient in the ocean. The global Si cycle plays a critical role in regulating primary productivity and carbon cycling on the continents and in the oceans. Development of the analytical tools used to study the sources, sinks, and fluxes of the global Si cycle (e.g., elemental and stable isotope ratio data for Ge, Si, Zn, etc. have recently led to major advances in our understanding of the mechanisms and processes that constrain the cycling of Si in the modern environment and in the past. Here, we provide background on the geochemical tools that are available for studying the Si cycle and highlight our current understanding of the marine, freshwater and terrestrial systems. We place emphasis on the geochemistry (e.g., Al/Si, Ge/Si, Zn/Si, δ13C, δ15N, δ18O, δ30Si of dissolved and biogenic Si, present case studies, such as the Silicic Acid Leakage Hypothesis, and discuss challenges associated with the development of these environmental proxies for the global Si cycle. We also discuss how each system within the global Si cycle might change over time (i.e., sources, sinks, and processes and the potential technical and conceptual limitations that need to be considered for future studies.

  20. Investigations on boron isotopic geochemistry of salt lakes in Qaidam basin, Qinghai

    Digital Repository Service at National Institute of Oceanography (India)

    Xiao, Y; Shirodkar, P.V.; Liu, W.G.; Wang, Y; Jin, L.

    of brine and are related to boron origin, the corrosion of salt and to certain chemical constituents. The distribution of boron isotopes in Quidam Basin showed a regional feature: salt lake brines in the west and northwest basin have the highest d11B values...

  1. Isotope geochemistry of waters affected by mining activities in Sierra Minera and Portman Bay (SE, Spain)

    International Nuclear Information System (INIS)

    García-Lorenzo, Mari Luz; Martínez-Sánchez, María José; Pérez-Sirvent, Carmen; Agudo, Inés; Recio, Clemente

    2014-01-01

    Highlights: • Waters have a meteoric origin even in samples located near the shore. • Marine infiltration only takes place in the deepest layers. • Sulfate enrichment was caused by oxidative dissolution of pyrite by ferric iron. - Abstract: The objective of this work was to evaluate processes affecting waters from Portman Bay by way of stable isotopic analysis, particularly H and O stable isotopes from water and S and O from dissolved sulfates. In addition, surface waters from Sierra Minera were examined for the purpose of determining if these waters are affected by similar processes. The results obtained indicate that Portman Bay waters are meteoric, and marine infiltration only takes place in the deepest layers near the shore or if water remains stagnated in sediments with low permeability. The main source of sulfate was the oxidation of sulfides, resulting in the liberation of acid, sulfate and metals. In order to assess the mechanism responsible for sulfide oxidation, the stoichiometric isotope balance model and the general isotope balance model were tested, suggesting that the oxidation via Fe 3+ was predominant in the surface, and controlled by Acidithiobacillus ferrooxidans, while at depth, sulfate reduction occurred

  2. The Use of Lead Isotope and Rare Earth Element Geochemistry for Forensic Geographic Provenancing

    Science.gov (United States)

    Carey, A.; Darrah, T.; Harrold, Z.; Prutsman-Pfeiffer, J.; Poreda, R.

    2008-12-01

    Lead isotope and rare earth element composition of modern human bones are analyzed to explore their utility for geographical provenancing. DNA analysis is the standard for identification of individuals. DNA analysis requires a DNA match for comparison. Thus, DNA analysis is of limited use in cases involving unknown remains. Trace elements are incorporated into bones and teeth during biomineralization, recording the characteristics of an individual's geochemical environment. Teeth form during adolescence, recording the geochemical environment of an individual's youth. Bones remodel throughout an individual's lifetime. Bones consist of two types of bone tissue (cortical and trabecular) that remodel at different rates, recording the geochemical environment at the time of biomineralization. Cortical bone tissue, forming the outer surface of bones, is dense, hard tissue that remodels in 25-30 yrs. Conversely, trabecular bone tissue, the inner cavity of bones, is low density, porous and remodels in 2-5 years. Thus, analyzing teeth and both bone tissues allows for the development of a geographical time line capable of tracking immigration patterns through time instead of only an individual's youth. Geochemical isotopic techniques (Sr, O, C, N) have been used for geographical provenancing in physical anthropology. The isotopic values of Sr, C, O, N are predominantly a function of soil compositions in areas where food is grown or water is consumed. Application of these provenancing techniques has become difficult as an individual's diet may reflect the isotopic composition of foods obtained at the local grocer as opposed to local soil compositions. Thus, we explore the use of REEs and Pb isotopes for geographical provenancing. Pb and REEs are likely more reliable indicators of modern geographical location as their composition are high in bio-available sources such as local soils, atmospheric aerosols, and dust as opposed to Sr, C, O, N that are controlled by food and

  3. Groundwater geochemistry of nile delta-desert interface 1.isotope hydrology

    Energy Technology Data Exchange (ETDEWEB)

    Hussein, M F [Cairo University, Dept., of Soil and water, Giza, Gamma Street, (Egypt); Nada, A A; Awad, M A [Atomic Energy Authority, Nuclear Chemistry Dept., P.o. Box 13759, Cairo, (Egypt)

    1995-10-01

    Sustenance and environmental protection of groundwater supply is of major concern in the integral environmental development in the arid to sub-arid regions in the Nile basin. Isotope data ({sup 18O}, {sup 2H} and {sup 3H}) of groundwater in the west of the Nile delta indicates the contribution of palaeo groundwater component (in the range 0.1 - 0.8 with means of 0.39 and 0.52 for tahrir and khatatbah, respectively) along with sub recent recharge from the delta aquifer and recent recharge from irrigation conveyance canals in desert. Isotope mixing model (developed as Two-input table using excel{sup TM} spreads heat on apple Macintosh{sup TM)} is proposed to explain the apparent discrepancies in groundwater isotopic composition of khatatbah and tahrir areas assuming the contribution of two isotopically different palaeo-oples with two isotopically similar maind delta groundwater poles. About 0.30% {sup 1}8{sup O} depletion per 10 Km downstream is detected and low northward groundwater recharge is suggested along 75 Km of the western strip of rosetta Nile. Higher sub-recent recharge from the main delta aquifer is believed to take place in khatatbah than tahrir whereas the last is believed to be replenished at present from the irrigation/ drainage network and irrigated fields with higher pollution risk for groundwater system in tahrir aquifer is exposed to northern marine intrusion. Lowering of the piezo metric level is to be expected in the newly exploited desertic areas under over pumping. 9 figs.

  4. Isotope geochemistry of waters affected by acid mine drainage in old labour sites (SE, Spain).

    Science.gov (United States)

    Pérez-Sirvent, Carmen; Martinez-Sanchez, Maria Jose; Garcia-Lorenzo, Maria Luz; Agudo, Ines; Hernandez-Cordoba, Manuel; Recio, Clemente

    2015-04-01

    The ore deposits of this zone have iron, lead and zinc as the main metal components. Iron is present in oxides, hydroxides, sulfides, sulfates, carbonates, and silicates; lead and zinc occur in sulfides (galena and sphalerite, respectively), carbonates, sulfates, and lead or zinc-bearing (manganese, iron) oxides. Mining started with the Romans and activity peaked in the second half of the 19th century and throughout the 20th century until the 1980's. From 1940 to 1957, mineral concentration was made by froth flotation and, prior to this, by gravimetric techniques. The mining wastes, or tailings, with a very fine particle size were deposited inland (tailings dams) and, since 1957, huge releases were made in directly the sea coast. The objective of this work was to evaluate processes affecting waters from abandoned mine sites by way of stable isotopic analysis, particularly H and O stable isotopes from water and S and O from dissolved sulfates. Several common chemical and physical processes, such as evaporation, water-rock interaction and mixing could alter water isotopic composition. Evaporation, which causes an enrichment in δD and δ18O in the residual water, is an important process in semiarid areas. The results obtained indicate that, for sites near the coast, waters are meteoric, and marine infiltration only takes place in the deepest layers near the shore or if water remains stagnated in sediments with low permeability. The main source of sulfate was the oxidation of sulfides, resulting in the liberation of acid, sulfate and metals. In order to assess the mechanism responsible for sulfide oxidation, the stoichiometric isotope balance model and the general isotope balance model were tested, suggesting that the oxidation via Fe3+ was predominant in the surface, and controlled by A. ferrooxidans, while at depth, sulfate reduction occurred.

  5. Boron geochemistry from some typical Tibetan hydrothermal systems: Origin and isotopic fractionation

    International Nuclear Information System (INIS)

    Zhang, Wenjie; Tan, Hongbing; Zhang, Yanfei; Wei, Haizhen; Dong, Tao

    2015-01-01

    The Tibetan plateau is characterized by intense hydrothermal activity and abnormal enrichment of trace elements in geothermal waters. Hydrochemistry and B isotope samples from geothermal waters in Tibet were systematically measured to describe the fractionation mechanisms and provide constraints on potential B reservoirs. B concentrations range from 0.35 to 171.90 mg/L, and isotopic values vary between −16.57 ‰ and +0.52 ‰. Geothermal fields along the Indus-Yarlung Zangbo suture zone and N–S rifts are observed with high B concentrations and temperatures. The similar hydrochemical compositions of high-B geothermal waters with magmatic fluid and consistent modeling of B isotopic compositions with present δ"1"1B values imply that the B in high-B geothermal waters is mainly contributed by magmatic sources, probably through magma degassing. In contrast, geothermal fields in other regions of the Lhasa block have relatively low B concentrations and temperatures. After considering the small fractionation factor and representative indicators of Na/Ca, Cl/HCO_3, Na + K and Si, the conformity between modeling results and the isotopic compositions of host rocks suggests that the B in low-temperature geothermal fields is mainly sourced from host rocks. According to simulated results, the B in some shallow geothermal waters not only originated from mixing of cold groundwater with deep thermal waters, but it was also contributed by equilibration with marine sedimentary rocks with an estimated proportion of 10%. It was anticipated that this study would provide useful insight into the sources and fractionation of B as well as further understanding of the relationships between B-rich salt lakes and geothermal activities in the Tibetan plateau. - Highlights: • Chemical and boron isotopic data of geothermal waters in Tibetan plateau were introduced. • Unusual enrichment of boron in Tibetan geothermal waters is related to magmatic and host rocks. • Boron

  6. Isotope and minor element geochemistry of high arsenic groundwater from Hangjinhouqi, the Hetao Plain, Inner Mongolia

    International Nuclear Information System (INIS)

    Deng Yamin; Wang Yanxin; Ma Teng

    2009-01-01

    High As groundwater is widely distributed in the northwestern Hetao Plain, an arid region with slow groundwater flow. Arsenic concentration in groundwater ranges from 1 to 1000 μg/L. Most water samples have elevated salinities, with Cl and/or HCO 3 as the dominant anions and Na as the dominant cation. High concentrations of As in shallow aquifers are associated with strongly reducing conditions, as evidenced by high concentrations of dissolved organic C (DOC), NH 4 , dissolved sulfide, arsenite and dissolved CH 4 , and relatively low concentrations of NO 3 - and SO 4 2- . Results of the hydrochemical, and H and O isotope geochemical studies indicate that evapotranspiration is an important process controlling the enrichment of Na and Cl as well as trace elements such as As, B, F and Br in groundwater. In Na-HCO 3 -dominated groundwaters, As, B and F were enriched. Decades of irrigation using Yellow River water has resulted in elevation of the groundwater level, which has accelerated salt accumulation in shallow groundwater and surface soil. In addition, irrigation is responsible for the release of some components from aquifer materials and mixing with saline groundwaters, as indicated by minor element and isotope geochemical data. Used to trace groundwater flow paths, Sr isotope composition also indicates that bedrock weathering is one of the primary sources of As in groundwater in the study area.

  7. Carbon isotope geochemistry of the Cretaceous-Tertiary section of the Wasserfallgraben, Lattengebirge, southeast Germany

    International Nuclear Information System (INIS)

    Arneth, J.D.; Matzigkeit, U.; Boos, A.

    1985-01-01

    Carbonates and organic matter in sediments of the Cretaceous-Tertiary (C/T) section of the Wasserfallgraben, Lattengebirge (Bavaria) have been investigated. All parameters - the carbonate content (Csub(carb)), its isotopic composition (delta 13 Csub(carb),delta 18 Osub(carb)) as well as the organic carbon content (Csub(org)), its isotopic composition (delta 13 Csub(org)) and the H/C ratio of the sedimentary organic matter - display systematic variations across the C/T boundary which cannot be attributed to a single cause. The boundary zone as a whole is tectonically disturbed and shows significant features of detrital contaminations. Unidirectional shift in delta 13 Csub(carb) and delta 13 Csub(org) are observed when directly comparing Maastrichtian (latest Cretaceous) and Danian (earliest Tertiary) sediments. These synchronous isotope displacements towards more negative readings are interpreted to reflect the reduced photosynthetic activity as consequence of the mass extinction at the C/T boundary. The results may have some bearings on other C/T profiles investigated where measurements on the reduced carbon species are still lacking. (orig.)

  8. Geochemistry and isotope hydrology of groundwaters in the Stripa Granite: results and preliminary interpretation

    International Nuclear Information System (INIS)

    Fritz, P.; Barker, J.F.; Gale, J.E.

    1979-04-01

    The results of geochemical and isotopic analyses on water samples from the granite at Stripa, Sweden, are presented. Groundwater samples collected from shallow, private wells; surface boreholes; and boreholes drilled from the 330 m and 410 m mine levels were analyzed for their major ion chemistry, dissolved gases, and environmental isotope contents. The principal change in the chemical load with depth is typified by chloride concentration, which increases from less than 5 mg/liter to about 300 mg/liter. There is a parallel increase in pH, which changes from about 6.5 to over 9.75. It is important to notice that calcite saturation is maintained and that, because of rising pH, dissolved inorganic carbon is lost. The total carbonate content thus decreases from about 70 mg/liter to less than 7 mg/liter. The 18 O and deuterium analyses demonstrate that different fracture systems contain different water masses, whose age increases with depth. Groundwater age determinations with 14 C and isotopes of the uranium decay series strongly indicate that water ages exceed 25,000 years. The 13 C contents of the aqueous carbonate in these groundwaters indicate groundwater recharge through vegetated soil, presumably during an interglacial period. The 13 C and 18 O determinations show that most fracture calcites have formed in a wide variety of depositional environments, and not in the waters circulating today

  9. Ca Isotope Geochemistry in Marine Deep Sea Sediments of the Eastern Pacific

    Science.gov (United States)

    Wittke, A.; Gussone, N. C.; Derigs, D.; Schälling, M.; Teichert, B. M.

    2017-12-01

    Ca isotope ratio analysis (δ44/40Ca) is a powerful tool to investigate diagenetic reactions in marine sedimentary porewater systems, as it is sensitive to processes such as carbonate dissolution, precipitation, recrystallization, ion exchange and deep fluid sources, due to the isotopic difference between dissolved Ca and solid carbonate minerals (e.g. [1];[2]). We analyzed eight sediment cores of the (paleo-) Pacific equatorial age transect. Two sediment cores show decreasing Ca isotope profiles starting at the sediment/water interface with seawater-like values down to sediment-like values due to recrystallization and an increasing in the bottom part again to seawater-like values. The other studied cores show different degrees of flattening of this middle bulge. We interpret this pattern either as an effect of sediment composition and thickness, decreasing recrystallization rates and/or fluid flux or a combination of all of these factors at the respective sampling sites. Element concentration profiles and Sr-isotope variations on some of these sediment cores show a similar behavior, supporting our findings ([3]; [4]). Seawater influx at (inactive) seamounts is supposed to cause seawater-like values at the bottom of the sediment cores by fluids migrating through the oceanic basement (e.g. [5]). While [6] hypothesizes that two seamounts or bathymetric pits are connected, with a recharge and a discharge site [7] say that uptaken fluids could be released through the surrounding seafloor as well due to diffusive exchange with the underlying oceanic crust. Our Ca isotope results combined with a transport reaction model approach support the latter hypothesis. References: [1] Teichert B. M., Gussone N. and Torres M. E. (2009) [2] Ockert C., Gussone N., Kaufhold S. and Teichert B. (2013) [3] Pälike H., Lyle M., Nishi H., Raffi I., Gamage K. and Klaus A. (eds.) (2010) [4] Voigt J., Hathorne E. C., Frank M., Vollstaedt H. and Eisenhauer A. (2015) [5] Villinger H. W

  10. The clumped-isotope geochemistry of exhumed marbles from Naxos, Greece

    Science.gov (United States)

    Ryb, U.; Lloyd, M. K.; Stolper, D. A.; Eiler, J. M.

    2017-07-01

    Exhumation and accompanying retrograde metamorphism alter the compositions and textures of metamorphic rocks through deformation, mineral-mineral reactions, water-rock reactions, and diffusion-controlled intra- and inter-mineral atomic mobility. Here, we demonstrate that these processes are recorded in the clumped- and single-isotope (δ13 C and δ18 O) compositions of marbles, which can be used to constrain retrograde metamorphic histories. We collected 27 calcite and dolomite marbles along a transect from the rim to the center of the metamorphic core-complex of Naxos (Greece), and analyzed their carbonate single- and clumped-isotope compositions. The majority of Δ47 values of whole-rock samples are consistent with exhumation- controlled cooling of the metamorphic complex. However, the data also reveal that water-rock interaction, deformation driven recrystallization and thermal shock associated with hydrothermal alteration may considerably impact the overall distribution of Δ47 values. We analyzed specific carbonate fabrics influenced by deformation and fluid-rock reaction to study how these processes register in the carbonate clumped-isotope system. Δ47 values of domains drilled from a calcite marble show a bimodal distribution. Low Δ47 values correspond to an apparent temperature of 260 °C and are common in static fabrics; high Δ47 values correspond to an apparent temperature of 200 °C and are common in dynamically recrystallized fabrics. We suggest that the low Δ47 values reflect diffusion-controlled isotopic reordering during cooling, whereas high Δ47 values reflect isotopic reordering driven by dynamic recrystallization. We further studied the mechanism by which dynamic recrystallization may alter Δ47 values by controlled heating experiments. Results show no significant difference between laboratory reactions rates in the static and dynamic fabrics, consistent with a mineral-extrinsic mechanism, in which slip along crystal planes was associated

  11. Neodymium and strontium isotopic stratigraphy of the neo-archean Rio Jacare Sill-Bahia, Brazil and its relation to PGE mineralization

    International Nuclear Information System (INIS)

    Brito, Reinaldo S.C de; Pimentel, Marcio M.; Nilson, Ariplinio A.; Gioia, Simone M

    2001-01-01

    Platinum-Group Elements (PGE) deposition in magma chambers is generally accepted as being triggered by sulphur immiscibility via sulfidasation and/or felsification of magmas. These processes can be related to fractional crystallization, and mixing of batches of magmas, crustal contamination or by the combination of these process. Important isotopic studies have been carried out by many authors such as Lambert (1989) and Marcantonio (1995) in the Stillwater Complex, Kruger and Marsh (1989) and Cawthorn (1996) in the Bushveld Complex. Those works set out to understand the role of isotopic changes in the genesis of PGE deposits from JM and Merensky Reefs, respectively. They attributed those PGE mineralizations to isotopically constrained mixing/contamination episodes associated to subtle changes in steady vertical fractionation trends. This work presents stratigraphycally-plotted Nd and Sr isotopic data together with evidence of mineral and whole rock geochemistry disturbance in smooth fractionations trends of the Rio Jacare Sill. Data interpretation suggest the sill was formed via fractional crystallisation and mixing of at least three magma batches, combined with some degree of host rocks assimilation. Isotopic changes were also related to PGE anomalies associated with transitional facies formed during such mixing episodes (au)

  12. Stratigraphy and stable isotope geochemistry of the carbonate sequence from the Paraguay belt

    International Nuclear Information System (INIS)

    Santos, Roberto Ventura.; Alvarenga, Carlos Jose Souza de; Dantas, Elton Luiz

    2001-01-01

    Two main Neoproterozoic carbonate sequences occur central Brazil both of which are stratiphicaly above glacial derived sediments. An older carbonate sequence occurs over the Sao Francisco Craton and in the surrounding folded belts (Rio Preto, Aracuai Ribeira and Brasilia). These carbonates overlie glacial diamictites that were related to the 'Sturtian' event dated between 0.7 and 0.9 Ga (Toulkeridis et al. 1999, Santos et al., 2000). A second carbonate sequence is described in the Paraguay Belt and postdated Vendian/Varegian glaciation sediments from the end of the Neoproterozoic. This glacial event has been reported in many studies concerning the Gondwana and the Laurentia supercontinent (Trompette, 1996; Condon and Prave, 2000; Myrow and Kaufman, 1999). In the Paraguay Belt the Vendian- Varangian glaciation rocks are characterized by a glaciomarine sequence, that occur at the border of the basin, and by glacial derived turbidites deposits, that occur in the deeper parts of the basin (Alvarenga and Trompette, 1992). Near the city of Corumba this glaciomarine sequence is overlaid by carbonate rocks containing Ediacaran-like fauna in which has been described Corumbella werneri and Cloudina Lucianoi (Hahn et al., 1982; Walde et al., 1982; Zaine and Fairchild, 1985; 1987). These carbonates have been interpreted as cap carbonates and the age of their fossils have been attributed to the Vendian Superior (590-545 MA) (Alvarenga and Trompette, 1992, Trompette 1996). Isotope stratigraphy studies have been widely used to study cap carbonate rocks that overlie Sturtian and Vendian- Varagian glaciogenic rocks. Stratigraphic correlation of these units is usually difficult because their lack fossils and there is no precise dating method that could be applied to these rocks. Hence, most studies concerning Neoproterozoic carbonates have concentrated on their stromatilites and microfossils content as well as on carbon isotope variations. In the present study, we present new carbon

  13. C–O Stable Isotopes Geochemistry of Tunisian Nonsulfide Zinc Deposits: A First Look

    Directory of Open Access Journals (Sweden)

    Hechmi Garnit

    2018-01-01

    Full Text Available A preliminary C–O stable isotopes geochemical characterization of several nonsulfide Zn-Pb Tunisian deposits has been carried out, in order to evidence the possible differences in their genesis. Nonsulfide ores were sampled from the following deposits: Ain Allegua, Jebel Ben Amara, Jebel Hallouf (Nappe Zone, Djebba, Bou Grine, Bou Jaber, Fedj el Adoum, Slata Fer (Diapir Zone, Jebel Ressas, Jebel Azreg, Mecella (North South Axis Zone, Jebel Trozza, Sekarna (Graben Zone. After mineralogical investigation of selected specimens, the C–O stable isotopic study was carried out on smithsonite, hydrozincite, cerussite and calcite. The data have shown that all the carbonate generations in the oxidized zones of Ain Allegua and Jebel Ben Amara (Nappe Zone, Bou Jaber, Bou Grine and Fedj el Adoum (Diapir Zone, Mecella and Jebel Azreg (North South Zone have a supergene origin, whereas the carbonates sampled at Sekarna (Graben Zone (and in limited part also at Bou Jaber precipitated from thermal waters at moderately high temperature. Most weathering processes that controlled the supergene alteration of the Zn-Pb sulfide deposits in Tunisia had probably started in the middle to late Miocene interval and at the beginning of the Pliocene, both periods corresponding to two distinct tectonic pulses that produced the exhumation of sulfide ores, but the alteration and formation of oxidized minerals could have also continued through the Quaternary. The isotopic characteristics associated with the weathering processes in the sampled localities were controlled by the different locations of the sulfide protores within the tectonic and climatic zones of Tunisia during the late Tertiary and Quaternary.

  14. Isotope geochemistry of drainage from an acid mine impaired watershed, Oakland, California

    International Nuclear Information System (INIS)

    Butler, Thomas W.

    2007-01-01

    Oxidation of sulfides at the Leona Heights Sulfur Mine has resulted in the liberation of acid, SO 4 and metals to Leona Creek. Previous research at the site has indicated Fe(II) oxidation at rates faster than would be predicted by abiotic oxidation alone, particularly in the segment of stream between the Adit and Leona Street sample stations. In order to assess the mechanisms responsible for sulfide oxidation, samples were collected for isotopic analysis of water and SO 4 , the results of which were used to develop a stoichiometric isotope-balance model. This exercise indicated that the percentage of water-derived oxygen in SO 4 increased spatially from between 56% and 64% at the Adit to between 71% and 72% at Leona Street, illustrating that increased sulfide oxidation via Fe(III) was occurring within, or as water flows over, the waste rock, relative to water emanating directly from the former mine. The incorporation of water-derived oxygen in SO 4 during pyrite oxidation is a process controlled by Fe oxidizing bacteria such as A. ferrooxidans at low pH. The role of bacteria was further supported by estimates of the rate constant for Fe oxidation between sampling stations, yielding values that were approximately 10 6 faster than abiotic Fe oxidation alone. Stable isotopic analysis of water further indicates a close correlation of adit spring water to the local meteoric water line, while 3 H data indicate a groundwater apparent age, or time of travel from its primary zone of recharge, of 34 S data, in conjunction with reported albitized feldspars within the Leona Rhyolite host rock, indicate a magmatic origin of ore sulfur, contrary to previous interpretations at the site

  15. Geochemistry of trace elements and Sr- Nd isotopes of foraminifera shell from the Okinawa Trough

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Trace elemental associations and Sr - Nd isotopic compositions are of important to recognition of biogenic material from mixed marine sediments. The foraminifera shell from the Okinawa Trough strongly enrichesSr, P, Mn andBa, enriches Li, U, Th, Sc, Co, Cu, Pb, Zn, Cr, Rb, Y, Sb and light rare earth elements, slightly enriches V, Ga, Zr, Nb, Cd and middle rare earth elements,is short of Mo, In, Sn, Cs, Hf, Ta, W, Ti, Bi and heavy rare earth elements. The mechanism of elemental enrichment in forminifera is the concentrations of trace elements in sea water and selective absorption of trace elements during foraminifera living, as well as the geochemical affinity between major elements and trace elements. The REE (rare earth elements) partition pattern of foraminifera shell of the Okinawa Trough shows enrichment of middle rare earth elements with slightly negative Ce anomaly,which are different from those of foraminifera of the Pacific Ocean. The Sr, Nd isotopic ratios of the Okinawa Trough foraminifera are 0.709 769 and 0.512 162, respectively, which are different not only from those of oceanic water, but also from those of river water of China's Mainland, the former is slightly higher than those of oceanic water, but much lower than those of river water; the latter is slightly lower than those of oceanic water, but higher than those of river water, demonstrating that the Okinawa Trough sea water has been influenced by river water of China's Mainland.

  16. Geochemistry and environmental isotope of groundwater from the upper Cretaceous aquifer of Orontes basin (Syria)

    International Nuclear Information System (INIS)

    Al-Charideh, A.

    2010-03-01

    Chemical and environmental isotopes have been used for studying the Upper Cretaceous aquifer systems in the Middle Orontes basin. The results indicate that the salinity of groundwater (0.2 to 2 g/l) reveals the dissolution of evaporate rocks is the main factor of high salinity especially in the Homes depression. The degree of salinity and its spaces distribution are basically related to the pattern of groundwater movement in the Upper cretaceous aquifer. The stable isotopes composition of groundwater in the Homes depression are more depleted by -2.5% and -17.0% for δ 18 O and δ 2 H respectively, than the groundwater from Hama elevation, suggested different origin and recharge time between this two groundwater groups. Estimates of their mean subsurface residence times have been constrained on the basis of 14 C D IC. The corrected ages of groundwater are recent and less to 10 thousand years in Hama uplift. However, the corrected age of groundwater in the Homs depression range between 10 to 25 thousand years indicate late Pleistocene recharge period. (author)

  17. An investigation of the stable isotopes, geochemistry and morphology of major streams in Dominica, Lesser Antilles: 2014 - 2017

    Science.gov (United States)

    Kopas, D. C.; Joseph, E. P.; Frey, H. M.

    2017-12-01

    The island of Dominica is a recently active (pH and temperature, were recorded and water samples taken and analyzed for alkalinity, major elements (cations and anions), trace elements and stable isotopes (carbon, deuterium, and oxygen). Variations in water chemistry and river morphology were compared to various parameters, including precipitation, landslide locations, and lithology for each of the catchments. Within the study period, on August 27th, 2015, a significant tropical storm, Erika, made landfall in Dominica, depositing more than 500 mm of rainfall in 10 hours. There was little infiltration of the rainwater (over 50-60% run-off), which resulted in significant landslides, flash floods and damage to infrastructure and loss of life. Despite the obvious morphologic changes to the streams and high discharge during the storm event, preliminary analysis has shown little change in major stream geochemistry following the passage of Tropical Storm Erika. The 10-month time gap between the storm and the post-storm field sampling in June 2016 may be a factor of why geochemical changes were not observed. One of the most significant variations of stream composition during the study period was annual shifts in δD between -1.3 to -5.8 ‰ and δ18O between -1.98 to -2.61 ‰. A possible factor influencing the δ18O of surface waters is seasonal variation in rainfall. The dominant control on precipitation δ18O values is the amount effect, whereby rainfall amount and δ18O are inversely correlated. This relationship is a proxy for changes in δ18O values of surface waters. The data also suggest that hydrothermal fluids are not a prominent contributor to Dominican rivers, despite the presence of active volcanism and numerous hydrothermal systems on the island. The exceptions are the White River, which drains the Valley of Desolation and Boiling Lake and the Lamothe River, which drains the Cold Soufrierre.

  18. Possible influence of clay contamination on B isotope geochemistry of carbonaceous samples

    International Nuclear Information System (INIS)

    Deyhle, Annette; Kopf, Achim

    2004-01-01

    The authors report results from an experimental study on mixtures of pure endmembers of natural clay and carbonate. The scientific rationale is an evaluation as to what extent B contents and B isotopes of carbonate samples may be obscured as a result of contamination with clay, particularly since both authigenic carbonates and biogenic carbonates (e.g. microfossil tests) often contain some clay. Three aliquots of a series of samples (each containing 0, 20, 40, 60, 80, 100% clay) were analyzed. Set 1 was washed with distilled, de-ionized water; for set 2 the HCl soluble parts were dissolved in 2 M HCl after washing; set 3 was completely digested with 30M HF prior to a series of ion exchanges. Isotope data of the endmembers are 6.6 per mille (100% marble) and -4.6%o (100% clay), with the clay being the dominant B source (ca. 50 ppm compared with 11 B adsorbed =12.9-14.1%o±0.5%o), while no B was mobilized from the carbonate. The HCl-dissolvable B in washed samples of set 2 show slightly increasing B contents with higher clay contents, suggesting that dissolution of the marble as well as B mobilization from the clay account for this trend. δ 11 B isotopes tend towards more negative values when clay content increases, indicating that some structurally-bound B is lost from the sheets of linked (Si, Al)O 4 tetrahedra of the clay mineral. This result shows that not only B adsorption, but possibly diffusion or weathering of broken edges of clay minerals releases some structurally bound B of clay minerals. Set 3, where bulk samples were completely HF-digested, shows as expected a linear increase in B concentrations and decreasing δ 11 B ratios with increasing clay content. The overall results suggest that relatively small amounts of clay (e.g. as contamination in a microfossil test) have no significant impact on the B content and δ 11 B measured for the carbonate, but that care has to be taken if clay exceeds 10wt.% (e.g. carbonate concretions, chimneys, etc.)

  19. Isotopic and hydro geochemistry research in ground water from Provincia de Entre Rios (Republica Argentina)

    International Nuclear Information System (INIS)

    Tujchneider, Ofelia Clara; Carmen Paris, Marta del; Fili, Mario Felipe; D'Elia, Monica Patricia

    1994-01-01

    In order to study the groundwater dynamics of the Northwest of the Entre Rios Province (Republica Argentina), supported on the regional knowledge resulting from previous reports, a detailed investigation is developed. The most important aquifer of the region, conformed by sands of the Ituzaingo and Parana Formations (Mioceno-Plioceno) underlies Hernandarias Formation (Pleistoceno) thick clays cover. This confinement condition, and the complex hydrodynamic behaviour as a result of the heterogeneity of the hydrogeological sequence, impeded determine with clearness the existence of actual and direct connections with the exterior cycle. The application of classical geohydrochemical methodologies complemented with both isotopic and heavy metals measurements, and data geostatistical processing, allows to formulate hypothesis about groundwater origin and the incidence of the autochthonous recharge. (author)

  20. Stable isotope geochemistry and evidence for meteoric diagenesis in Kudankulam formation, Tamil Nadu

    International Nuclear Information System (INIS)

    Armstrong Altrin Sam, J.; Ramasamy, S.; Makhnach, A.

    2001-01-01

    The results obtained from stable isotope study of Neogene carbonates of Kudankulam, Tamil Nadu show negative values for δ 13c arbon, which range from -2.6% to -9.7% PDB. The δ 18O values range from -4.5% to -11.4% PDB. The depleted nature of the δ 18O and δ 13C values suggests the strong effect of meteoric diagenesis in the Kudankulam carbonates. Standard bivariate plots of δ 18O versus δ 13C for carbonate materials/rocks helped to identify their depositional and diagenetic environments. Petrographic study points out large-scale emplacement of ferroan sparry calcite cement into vugs and other leached cavities. (author)

  1. Isotopic and hydro geochemistry study of the granular aquifer from Comarca Lagunera, Mexico

    International Nuclear Information System (INIS)

    Gonzalez Hita, Luis; Sanchez Diaz, Luis Felipe

    1994-01-01

    The Comarca Lagunera is one of Mexico's biggest agricultural regions. Its water sources are the Nazas and Aguanaval Rivers and a quaternary granular aquifer. The over exploitation of the aquifer has led to deteriorated groundwater quality due to the presence of arsenic. This study aims to determine the origin and evolution of the arsenic and to update the system's hydrogeochemical information. The methodology used is based on an analysis of the physical framework and on the hydrogeochemical and isotope characterization of the groundwater. An interpretation of the results shows that the arsenic could have originated in two geological events: first, the magmatic processes that generated the region's intrusive and extrusive igneous rocks, and second, the sedimentation of alluvial-lacustrine materials bearing arsenic, which were transported by the Nazas and Aguanaval Rivers during the aquifer's formation. (author)

  2. The Itataia phosphate-uranium deposit (Ceará, Brazil) new petrographic, geochemistry and isotope studies

    Science.gov (United States)

    Veríssimo, César Ulisses Vieira; Santos, Roberto Ventura; Parente, Clóvis Vaz; Oliveira, Claudinei Gouveia de; Cavalcanti, José Adilson Dias; Nogueira Neto, José de Araújo

    2016-10-01

    The Itataia phosphate-uranium deposit is located in Santa Quitéria, in central Ceará State, northeastern Brazil. Mineralization has occurred in different stages and involves quartz leaching (episyenitization), brecciation and microcrystalline phase formation of concretionary apatite. The last constitutes the main mineral of Itatiaia uranium ore, namely collophane. Collophanite ore occurs in massive bodies, lenses, breccia zones, veins or episyenite in marble layers, calc-silicate rocks and gneisses of the Itataia Group. There are two accepted theories on the origin of the earliest mineralization phase of Itataia ore: syngenetic (primary) - where the ore is derived from a continental source and then deposited in marine and coastal environments; and epigenetic (secondary) - whereby the fluids are of magmatic, metamorphic and meteoric origin. The characterization of pre- or post-deformational mineralization is controversial, since the features of the ore are interpreted as deformation. This investigation conducted isotopic studies and chemical analyses of minerals in marbles and calc-silicate rocks of the Alcantil and Barrigas Formations (Itataia Group), as well as petrographic and structural studies. Analysis of the thin sections shows at least three phosphate mineral phases associated with uranium mineralizaton: (1) A prismatic fluorapatite phase associated with chess-board albite, arfvedsonite and ferro-eckermannite; (2) a second fluorapatite phase with fibrous radial or colloform habits that replaces calcium carbonate in marble, especially along fractures, with minerals such as quartz, chlorite and zeolite also identified in calc-silicate rocks; and (3) an younger phosphate phase of botryoidal apatite (fluorapatite and hydroxyapatite) related with clay minerals and probably others calcium and aluminum phosphates. Detailed isotopic analysis carried out perpendicularly to the mineralized levels and veins in the marble revealed significant variation in isotopic

  3. Compilation of gas geochemistry and isotopic analyses from The Geysers geothermal field: 1978-1991

    Science.gov (United States)

    Lowenstern, Jacob B.; Janik, Cathy; Fahlquist, Lynne; Johnson, Linda S.

    1999-01-01

    We present 45 chemical and isotopic analyses from well discharges at The Geysers geothermal field and summarize the most notable geochemical trends. H2 and H2S concentrations are highest in the Southeast Geysers, where steam samples have δD and δ18O values that reflect replenishment by meteoric water. In the Northwest Geysers, samples are enriched in gas/steam, CO2, CH4, and N2/Ar relative to the rest of the field, and contain steam that is elevated in δD and δ18O, most likely due to substantial contributions from Franciscan-derived fluids. The δ13C of CO2, trends in CH4 vs. N2, and abundance of NH3 indicate that the bulk of the non-condensable gases are derived from thermal breakdown of organic materials in Franciscan meta-sediments.

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

    International Nuclear Information System (INIS)

    Gastal, M.C.P.; Macambira, M.J.B.; Medeiros, H.; Dall'Agnol, R.

    1987-01-01

    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 87 Sr/ 86 Sr 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) [pt

  5. Geochronology, radiogenic isotope geochemistry, and petrogenesis of Sang bast Paleo-tethys monzogranite, Mashhad, Iran

    International Nuclear Information System (INIS)

    Karimpour, M. H.; Farmer, G.L.; Stern, C.R.

    2010-01-01

    The study area is located in northeastern Iran (south of Mashhad). Paleo-Tethys Ocean opened during Silurian time and subduction under Turan plate was started in Late Devonian. By Late Triassic (225 Ma) there was no Paleo-Tethys left on an Iranian transect, therefore Turan plate obducted over Iran Plate. Two stages of low grade regional metamorphism are exposed, that are related to Hercynian (Late Paleozoic) and Cimmerian (Jurassic) oro genies. The Paleo-Tethys remnants (meta-ophiolite and meta-flysch) were intruded by Sang bast monzogranite. Chemically, monzogranite is moderately peraluminous S-type granitoid. It has low values of magnetic susceptibility [(5 to 11) * 10 -5 SI] therefore it is classified as belonging to the ilmenite-series of reduced type granitoids. Monzogranite is characterized by strong light rare earth element enrichment and less low heavy rare earth element. All samples have very small negative Eu anomalies (Eu/Eu * = 0.62 to 0.88). Total rare earth element content of monzogranite is between 212-481 ppm. The result of U-Pb zircon age dating of monzogranite is 201.3 ± 3.6 Ma (Upper Triassic, Rhaetian time). The initial 87 Sr/ 86 Sr and 143 Nd/ 144 Nd ratios for monzogranite is (0.706776 and 0.512219) when recalculated to an age of 201 Ma, consistent with the new radiometric. The initial 87 Sr/ 86 Sr and 143 Nd/ 144 Nd ratios for slate is (0.720613 and 0.511601) respectively when recalculated to an age of 201 Ma, consistent with the new radiometric results. Initial εNd isotope values for monzogranite is -3.13 and the slate is -15.19. Based on radiogenic isotopic data and rare earth element monzogranite magma originated either from lower continental crust which was very different from slate or it is originated from mantle and contaminated in continental crust during ascending.

  6. Simulating the Transfer of Strontium-90 from Soil to Leafy Vegetables by Using Strontium-88

    OpenAIRE

    Kuke, Ding; Shujuan, Liu; Yingxue, He; Dong, Yan; Fengshou, Zhang; Shuifeng, Wang; Jinghua, Guo; Wei, Zhang; Xin, Wang; Xiaoyan, Jiang

    2016-01-01

    The transfer, from soil to Chinese cabbage and spinach, of radioactive strontium-90 released as a result of accidents in nuclear power stations was studied using a stable isotope of strontium, namely nuclide strontium-88 (88Sr). The study led to an experimental model for assessing the hazard of radionuclide strontium-90 (90Sr) entering the food chain and for predicting the risk to food safety. Chinese cabbage and spinach were grown in pots in a greenhouse and irrigated with deionized water co...

  7. Mass measurements of neutron-rich strontium and rubidium isotopes in the region $A \\approx 100$ and development of an electrospray ionization ion source

    CERN Document Server

    de Roubin, Antoine

    An extension of the atomic mass surface in the region $A \\approx 100$ is performed via mass measurements of the $^{100−102}$Sr and $^{100−102}$Rb isotopes with the ion-trap mass spectrometer ISOLTRAP at CERN-ISOLDE. The first direct mass measurements of $^{102}$Sr and $^{101,102}$Rb are reported here. These measurements confirm the continuation of the region of nuclear deformation with the increase of neutron number, at least as far as $N = 65$. In order to interpret the deformation in the strontium isotopic chain and to determine whether an onset of deformation is present in heavier krypton isotopes, a comparison is made between experimental values and theoretical calculations available in the literature. To complete this comparison, Hartree-Fock-Bogoliubov calculations for even and odd isotopes are also presented, illustrating the competition of nuclear shapes in the region. The development of an electrospray ionization ion source is presented. This source can deliver a large range of isobaric masses ...

  8. The Ellsworth terrane, coastal Maine: Geochronology, geochemistry, and Nd-Pb isotopic composition - Implications for the rifting of Ganderia

    Science.gov (United States)

    Schulz, K.J.; Stewart, D.B.; Tucker, R.D.; Pollock, J.C.; Ayuso, R.A.

    2008-01-01

    The Ellsworth terrane is one of a number of fault-bounded blocks that occur along the eastern margin of Ganderia, the western-most of the peri-Gondwanan domains in the northern Appalachians that were accreted to Laurentia in the Paleozoic. Geologic relations, detrital zircon ages, and basalt geochemistry suggest that the Ellsworth terrane is part of Ganderia and not an exotic terrane. In the Penobscot Bay area of coastal Maine, the Ellsworth terrane is dominantly composed of bimodal basalt-rhyolite volcanic sequences of the Ellsworth Schist and unconformably overlying Castine Volcanics. We use new U-Pb zircon geochronology, geochemistry, and Nd and Pb isotopes for these volcanic sequences to constrain the petrogenetic history and paleotectonic setting of the Ellsworth terrane and its relationship with Ganderia. U-Pb zircon geochronology for rhyolites indicates that both the Ellsworth Schist (508.6 ?? 0.8 Ma) and overlying Castine Volcanics (503.5 ?? 2.5 Ma) are Middle Cambrian in age. Two tholefitic basalt types are recognized. Type Tb-1 basalt, present as pillowed and massive lava flows and as sills in both units, has depleted La and Ce ([La/Nd]N = 0.53-0.87) values, flat heavy rare earth element (REE) values, and no positive Th or negative Ta anomalies on primitive mantle-normalized diagrams. In contrast, type Th-2 basalt, present only in the Castine Volcanics, has stightly enriched LREE ([La/Yb]N = 1.42-2.92) values and no Th or Th anomalies. Both basalt types have strongly positive ??Nd (500) values (Th-1 = +7.9-+8.6; Th-2 = +5.6-+7.0) and relatively enriched Pb isotopic compositions (206Ph/204Pb = 18.037-19.784; 207/204Pb = 15.531-15.660; 2088Pb/204Pb = 37.810-38.817). The basalts have compositions transitional between recent normal and enriched mid-ocean-ridge basalt, and they were probably derived by partial melting of compositionatly heterogeneous asthenosphenc mantle. Two types of rhyolite also are present. Type R-1 rhyolite, which mostly occurs as tuffs

  9. Feasibility study for the processing of Hanford Site cesium and strontium isotopic sources in the Hanford Waste Vitrification Plant

    International Nuclear Information System (INIS)

    Anantatmula, R.P.; Watrous, R.A.; Nelson, J.L.; Perez, J.M.; Peters, R.D.; Peterson, M.E.

    1991-09-01

    The final environmental impact statement for the disposal of defense-related wastes at the Hanford Site (Final Environmental Impact Statement: Disposal of Hanford Defense High-Level, Transuranic and Tank Wastes [HDW-EIS] [DOE 1987]) states that the preferred alternative for disposal of cesium and strontium wastes at the Hanford Site will be to package and ship these wastes to the commercial high-level waste repository. The Record of Decision for this EIS states that before shipment to a geologic repository, these wastes will be packaged in accordance with repository waste acceptance criteria. However, the high cost per canister for repository disposal and uncertainty about the acceptability of overpacked capsules by the repository suggest that additional alternative means of disposal be considered. Vitrification of the cesium and strontium salts in the Hanford Waste Vitrification Plant (HWVP) has been identified as a possible alternative to overpacking. Subsequently, Westinghouse Hanford Company's (Westinghouse Hanford) Projects Technical Support Office undertook a feasibility study to determine if any significant technical issues preclude the vitrification of the cesium and strontium salts. Based on the information presented in this report, it is considered technically feasible to blend the cesium chloride and strontium fluoride salts with neutralized current acid waste (NCAW) and/or complexant concentrate (CC) waste feedstreams, or to blend the salts with fresh frit and process the waste through the HWVP

  10. Organic geochemistry and stable isotope composition of New Zealand carbonate concretions and calcite fracture fills

    International Nuclear Information System (INIS)

    Pearson, M.J.; Nelson, C.S.

    2005-01-01

    Carbonate concretion bodies, representing a number of morphological types, and associated calcite fracture fills, mainly from New Zealand, have been studied both organically and inorganically. Extracted organic material is dominated by a complex polymeric dark brown highly polar fraction with a subordinate less polar and lighter coloured lipid fraction. The relative proportion of the two fractions is the principal control on the colour of fracture fill calcites. Concretions are classified mainly by reference to their carbonate stable carbon and oxygen isotope and cation composition. Typical subspherical calcitic septarian concretions, such as those in the Paleocene Moeraki and the Eocene Rotowaro Siltstones, contain carbon derived mainly by bacterial sulfate reduction in marine strata during early diagenesis. Other concretions, including a septarian calcitic type from the Northland Allochthon, have a later diagenetic origin. Siderite concretions, abundant in the nonmarine Waikato Coal Measures, are typically dominated by methanogenic carbon, whereas paramoudra-like structures from the Taranaki Miocene have the most extreme carbon isotope compositions, probably resulting from methane formation or oxidation in fluid escape conduits. Lipids from concretion bodies and most fracture fill calcites contain significant concentrations of fatty acids. Concretion bodies dominated by bimodally distributed n-fatty acids with strong even-over-odd preference, in which long chain n-acids are of terrestrial origin, have very low hydrocarbon biomarker maturities. Concretion bodies that lack long chain n-acids often have higher apparent biomarker maturity and prominent alpha-omega diacids. Such diacids are abundant in fracture fill calcites at Rotowaro, especially where calcite infills the septaria of a siderite concretion in the non-marine Waikato Coal Measures, and support the view that fluid transport resulted in carbonate entrapment of the fracture-hosted acids. Diacids also

  11. Sr isotope geochemistry of voluminous acidic pyroclastics erupted at 1-3 Ma in Northeast Japan

    International Nuclear Information System (INIS)

    Shirahase, Teruo; Tamanyu, Shiro; Togashi, Shigeko

    1989-01-01

    Sr isotope ratios are analyzed for voluminous acidic pyroclastics erupted at 1 - 3 Ma in five areas on the volcanic front of Northeast Japan. The initial values of 87 Sr/ 86 Sr ratios range from 0.7040 to 0.7055. There is no significant difference in ratios between 1 - 3 Ma acidic pyroclastics and 0 - 1 Ma andesitic volcanics in each area in spite of differences in age and in mean SiO 2 content. On the other hand, the ratios in both of 1 - 3 Ma and 0 - 1 Ma volcanics vary along arc in the same manner. The changes of Sr and Rb contents in each area are consistent with systematic changes by fractional crystallization. The low 87 Sr/ 86 Sr ratios and chemistry suggest that 1 - 3 Ma acidic pyroclastics of Northeast Japan formed by a high degree of fractional crystallization from basic magma which is common in genesis with young andesitic volcanism. The mechanisms of the formation of the basic magma and the character of mantle source in each area have not changed for the past 3 Ma. Degrees of fractional crystallization changed with changes of the tectonic condition of shallow magma chamber from a weak horizontal compression stress field to a strong one. (author)

  12. Geochemistry of CI chondrites: Major and trace elements, and Cu and Zn Isotopes

    Science.gov (United States)

    Barrat, J. A.; Zanda, B.; Moynier, F.; Bollinger, C.; Liorzou, C.; Bayon, G.

    2012-04-01

    In order to check the heterogeneity of the CI chondrites and determine the average composition of this group of meteorites, we analyzed a series of six large chips (weighing between 0.6 and 1.2 g) of Orgueil prepared from five different stones. In addition, one sample from each of Ivuna and Alais was analyzed. Although the sizes of the chips used in this study were “large”, our results show evidence for minor chemical heterogeneity in Orgueil, particularly for alkali elements and U. After removal of one outlier sample, the spread of the results is considerably reduced. For most of the 46 elements analyzed in this study, the average composition calculated for Orgueil is in very good agreement with previous CI estimates. This average, obtained with a “large” mass of samples, is analytically homogeneous and is suitable for normalization purposes. Finally, the Cu and Zn isotopic ratios are homogeneously distributed within the CI parent body with a spread of less than 100 ppm per atomic mass unit (amu).

  13. Isotope geochemistry of hydrothermal alteration in East of Esfahan, Central Iran

    Science.gov (United States)

    Taghipour, Sedigheh; Taghipour, Batoul

    2010-05-01

    In the Cenozoic magmatic belt of Central Iran, the Eocene volcanics and pyroclastics from the East of Esfahan underwent extensive hydrothermal alteration. The Eocene volcanics composed mostly of andesite lava and tuffs have been altered. The survey area is laterally zoned from an inner quartz-sericite alteration zone to an outer propylitic zone. Quartz-sericite alteration is predominant (>95%), but smaller zones of alunite-jarosite and silicified zones are present and superimposed onto a quartz-sericite alteration. In the quartz-sericite zone all altered rocks are light grayish to whitish in color and porphyritic with aphanitic groundmass. Concentrations of alunite and jarosite veinlets and stockworks are dispersed irregularly in this zone. Alunite and jarosite occur also as coatings on fractured rocks. All types of alunite occurrences are brick-red, cream, white and buff in colors, while jarosite is brown to rusty in colors. To verify, chemical composition of alunite and jarosite were identified by X-ray diffraction in mineral assemblages. Major alteration zones show inclusions of propylite, quartz sericite, advanced argillic and silicified zones. These alunites are mainly porcelaneous and their compositions show a solid solution between alunite and jarosite. In alteration zones, the mineral assemblage is characterized by alunite-jarosite + quartz + sericite + alkali feldspars + chlorite ± turquoise ± barite ± iron oxides. There are numerous alunite and jarosite occurrences, mainly as veinlets, in parts of the advanced argillic zone. Alunite δ18O and δ D values range from -1.76 to 8.81‰ and from -52.86 to -129.26‰ respectively. Field observations, mineralogical evidence and results from light element stable isotope data (δ18O, δ D and δ34S); indicate that in this area alunitization is supergene in origin.

  14. Radiocarbon and stable-isotope geochemistry of organic and inorganic carbon in Lake Superior

    Science.gov (United States)

    Zigah, Prosper K.; Minor, Elizabeth C.; Werne, Josef P.

    2012-03-01

    We present a lake-wide investigation of Lake Superior carbon and organic matter biogeochemistry using radiocarbon, stable isotope, and carbon concentrations. Dissolved inorganic carbon (DIC) abundance in the lake was 121-122 Tg C, with offshore concentration andδ13C values being laterally homogenous and tightly coupled to the physical and thermal regime and biochemical processes. Offshore Δ14C of DIC (50-65‰) exhibited lateral homogeneity and was more 14C enriched than co-occurring atmospheric CO2 (˜38‰); nearshore Δ14C of DIC (36-38‰) was similar to atmospheric CO2. Dissolved organic carbon (DOC) abundance was 14.2-16.4 Tg C. DOC's concentration and δ13C were homogenous in June (mixed lake), but varied laterally during August (stratification) possibly due to spatial differences in lake productivity. Throughout sampling, DOC had modern radiocarbon values (14-58‰) indicating a semilabile nature with a turnover time of ≤60 years. Lake particulate organic carbon (POC, 0.9-1.3 Tg C) was consistently 13C depleted relative to DOC. The δ15N of epilimnetic particulate organic nitrogen shifted to more negative values during stratification possibly indicating greater use of nitrate (rather than ammonium) by phytoplankton in August. POC's radiocarbon was spatially heterogeneous (Δ14C range: 58‰ to -303‰), and generally 14C depleted relative to DOC and DIC. POC 14C depletion could not be accounted for by black carbon in the lake but, because of its spatial and temporal distribution, is attributed to sediment resuspension. The presence of old POC within the epilimnion of the open lake indicates possible benthic-pelagic coupling in the lake's organic carbon cycle; the ultimate fate of this old POC bears further investigation.

  15. Annual and seasonal distribution of intertidal foraminifera and stable carbon isotope geochemistry, Bandon Marsh, Oregon, USA

    Science.gov (United States)

    Milker, Yvonne; Horton, Benjamin; Vane, Christopher; Engelhart, Simon; Nelson, Alan R.; Witter, Robert C.; Khan, Nicole S.; Bridgeland, William

    2014-01-01

    We investigated the influence of inter-annual and seasonal differences on the distribution of live and dead foraminifera, and the inter-annual variability of stable carbon isotopes (d13C), total organic carbon (TOC) values and carbon to nitrogen (C/N) ratios in bulk sediments from intertidal environments of Bandon Marsh (Oregon, USA). Living and dead foraminiferal species from 10 stations were analyzed over two successive years in the summer (dry) and fall (wet) seasons. There were insignificant inter-annual and seasonal variations in the distribution of live and dead species. But there was a noticeable decrease in calcareous assemblages (Haynesina sp.) between live populations and dead assemblages, indicating that most of the calcareous tests were dissolved after burial; the agglutinated assemblages were comparable between constituents. The live populations and dead assemblages were dominated by Miliammina fusca in the tidal flat and low marsh, Jadammina macrescens, Trochammina inflata and M. fusca in the high marsh, and Trochamminita irregularis and Balticammina pseudomacrescens in the highest marsh to upland. Geochemical analyses (d13C, TOC and C/N of bulk sedimentary organic matter) show no significant influence of inter-annual variations but a significant correlation of d13C values (R = 20.820, p , 0.001), TOC values (R = 0.849, p , 0.001) and C/N ratios (R = 0.885, p , 0.001) to elevation with respect to the tidal frame. Our results suggest that foraminiferal assemblages and d13C and TOC values, as well as C/N ratios, in Bandon Marsh are useful in reconstructing paleosea-levels on the North American Pacific coast.

  16. Experimental evidence shows no fractionation of strontium isotopes ((87)Sr/(86)Sr) among soil, plants, and herbivores: implications for tracking wildlife and forensic science.

    Science.gov (United States)

    Flockhart, D T Tyler; Kyser, T Kurt; Chipley, Don; Miller, Nathan G; Norris, D Ryan

    2015-01-01

    Strontium isotopes ((87)Sr/(86)Sr) can be useful biological markers for a wide range of forensic science applications, including wildlife tracking. However, one of the main advantages of using (87)Sr/(86)Sr values, that there is no fractionation from geological bedrock sources through the food web, also happens to be a critical assumption that has never been tested experimentally. We test this assumption by measuring (87)Sr/(86)Sr values across three trophic levels in a controlled greenhouse experiment. Adult monarch butterflies were raised on obligate larval host milkweed plants that were, in turn, grown on seven different soil types collected across Canada. We found no significant differences between (87)Sr/(86)Sr values in leachable Sr from soil minerals, organic soil, milkweed leaves, and monarch butterfly wings. Our results suggest that strontium isoscapes developed from (87)Sr/(86)Sr values in bedrock or soil may serve as a reliable biological marker in forensic science for a range of taxa and across large geographic areas.

  17. Crustal evolution of South American Platform based on Sm-Nd isotope geochemistry

    International Nuclear Information System (INIS)

    Sato, Kei

    1998-01-01

    Sm-Nd isotopic systematics is relevant to the topics of origin and evolution the of continental crust, where model ages refer to the time when crustal material was differentiated from the upper mantle. Alternative interpretations are due to a lack of adequate information on crustal processes and the variable composition of the mantle sources. The Sm-Nd methods are presented, and applied on rock materials from the South American Platform. The main conclusions indicate juvenile accretion with higher growth rates (peaks), around 3.7-3.5 Ga (∼ 0.5% in volume), 3.1 - 2.9 Ga (∼16%), 2.7 - 2.6 (∼ 9%), 2.2 - 1.9 (35%) and 1.3-1.0 (7%). The continental growth curve indicates that about 35 % of the crust was formed by 2.5 Ga, 88% by 1.8 Ga and 99% by 1.0 Ga, and the remaining ∼ 1 % was added in the Phanerozoic. Rapid crustal growth occurred between 2.2 and 1.9 Ga. The main period of continental crust formation occurred during the Paleoproterozoic, corresponding to 54 % in volume. Sm-Nd model ages, when compared with the crystallisation ages of granitoid rocks, furnish a rough estimate of juvenile vs. reworked material. Within the South American Platform about 45% of juvenile continental crust is still preserved within tectonic provinces of different ages. The remainder represents continental crust reworked in younger tectono-thermal events. In particular crustal reworking was predominating over juvenile accretion during Meso-Neoproterozoic. The Transbrasiliano Lineament is a megasuture, active in the Neoproterozoic, which separates a large northwestern mass, including the Amazonian and Sao Luis Cratons, from a southeastern mass, formed by a collage of cratonic fragments, of which the Sao Francisco and Rio de La Plata are the largest. The crustal evolutions of these two large continental masses are considered individually, and can be resumed following form: I - Old Archean rocks (>3.4 Ga) are found only within the south-eastern part (Gaviao Block, Contendas

  18. Determination of strontium isotopic composition in natural waters: examples of application in subsurface waters of the coastal zone of Bragantina region, Para, BR

    International Nuclear Information System (INIS)

    Bordalo, Adriana Oliveira; Moura, Candido Augusto Veloso; Scheller, Thomas

    2007-01-01

    Analytical procedures used for determining the concentrations and isotope composition of strontium in subsurface waters, by mass spectrometry, are described. Sampling was performed in coastal plateaus, salt marsh and mangrove environments in the coastal region of Para. Coastal plateau waters have δ 87 Sr between 1.51 and 6.26 per mille and Sr concentration bellow 58 ppb. Salt marsh waters show δ 87 Sr between 0.55 and 0.90 per mille and Sr concentration between 93 and 114 ppm, while mangrove waters have δ 87 Sr per mille around zero and Sr concentration above 15 ppm. Differences in the 87 Sr/ 86 Sr ratio in these subsurface waters are detected, as well as seasonal variations in the coastal plateau waters. (author)

  19. Seawater strontium isotope curve at the Silurian/Devonian boundary: a study of the global Silurian/Devonian boundary stratotype

    Czech Academy of Sciences Publication Activity Database

    Frýda, J.; Hladil, Jindřich; Vokurka, K.

    2002-01-01

    Roč. 35, č. 1 (2002), s. 21-28 ISSN 0016-6995 R&D Projects: GA ČR GA205/98/0454; GA ČR GA205/01/0143 Institutional research plan: CEZ:AV0Z3013912 Keywords : strontium chemostratigraphy * Silurian/Devonian * Barrandian area Subject RIV: DB - Geology ; Mineralogy Impact factor: 0.410, year: 2002

  20. STRONTIUM PRECIPITATION

    Science.gov (United States)

    McKenzie, T.R.

    1960-09-13

    A process is given for improving the precipitation of strontium from an aqueous phosphoric-acid-containing solution with nickel or cobalt ferrocyanide by simultaneously precipitating strontium or calcium phosphate. This is accomplished by adding to the ferrocyanide-containing solution calcium or strontium nitrate in a quantity to yield a concentration of from 0.004 to 0.03 and adjusting the pH of the solution to a value of above 8.

  1. Impacts of changes in groundwater recharge on the isotopic composition and geochemistry of seasonally ice-covered lakes: insights for sustainable management

    Science.gov (United States)

    Arnoux, Marie; Barbecot, Florent; Gibert-Brunet, Elisabeth; Gibson, John; Noret, Aurélie

    2017-11-01

    Lakes are under increasing pressure due to widespread anthropogenic impacts related to rapid development and population growth. Accordingly, many lakes are currently undergoing a systematic decline in water quality. Recent studies have highlighted that global warming and the subsequent changes in water use may further exacerbate eutrophication in lakes. Lake evolution depends strongly on hydrologic balance, and therefore on groundwater connectivity. Groundwater also influences the sensitivity of lacustrine ecosystems to climate and environmental changes, and governs their resilience. Improved characterization of groundwater exchange with lakes is needed today for lake preservation, lake restoration, and sustainable management of lake water quality into the future. In this context, the aim of the present paper is to determine if the future evolution of the climate, the population, and the recharge could modify the geochemistry of lakes (mainly isotopic signature and quality via phosphorous load) and if the isotopic monitoring of lakes could be an efficient tool to highlight the variability of the water budget and quality. Small groundwater-connected lakes were chosen to simulate changes in water balance and water quality expected under future climate change scenarios, namely representative concentration pathways (RCPs) 4.5 and 8.5. Contemporary baseline conditions, including isotope mass balance and geochemical characteristics, were determined through an intensive field-based research program prior to the simulations. Results highlight that future lake geochemistry and isotopic composition trends will depend on four main parameters: location (and therefore climate conditions), lake catchment size (which impacts the intensity of the flux change), lake volume (which impacts the range of variation), and lake G index (i.e., the percentage of groundwater that makes up total lake inflows), the latter being the dominant control on water balance conditions, as revealed by

  2. Impacts of changes in groundwater recharge on the isotopic composition and geochemistry of seasonally ice-covered lakes: insights for sustainable management

    Directory of Open Access Journals (Sweden)

    M. Arnoux

    2017-11-01

    Full Text Available Lakes are under increasing pressure due to widespread anthropogenic impacts related to rapid development and population growth. Accordingly, many lakes are currently undergoing a systematic decline in water quality. Recent studies have highlighted that global warming and the subsequent changes in water use may further exacerbate eutrophication in lakes. Lake evolution depends strongly on hydrologic balance, and therefore on groundwater connectivity. Groundwater also influences the sensitivity of lacustrine ecosystems to climate and environmental changes, and governs their resilience. Improved characterization of groundwater exchange with lakes is needed today for lake preservation, lake restoration, and sustainable management of lake water quality into the future. In this context, the aim of the present paper is to determine if the future evolution of the climate, the population, and the recharge could modify the geochemistry of lakes (mainly isotopic signature and quality via phosphorous load and if the isotopic monitoring of lakes could be an efficient tool to highlight the variability of the water budget and quality. Small groundwater-connected lakes were chosen to simulate changes in water balance and water quality expected under future climate change scenarios, namely representative concentration pathways (RCPs 4.5 and 8.5. Contemporary baseline conditions, including isotope mass balance and geochemical characteristics, were determined through an intensive field-based research program prior to the simulations. Results highlight that future lake geochemistry and isotopic composition trends will depend on four main parameters: location (and therefore climate conditions, lake catchment size (which impacts the intensity of the flux change, lake volume (which impacts the range of variation, and lake G index (i.e., the percentage of groundwater that makes up total lake inflows, the latter being the dominant control on water balance conditions, as

  3. Sources of metals in the Porgera gold deposit, Papua New Guinea: Evidence from alteration, isotope, and noble metal geochemistry

    Science.gov (United States)

    Richards, Jeremy P.; McCulloch, Malcolm T.; Chappell, Bruce W.; Kerrich, Robert

    1991-02-01

    The Porgera gold deposit is spatially and temporally associated with the Late Miocene, mafic, alkalic, epizonal Porgera Intrusive Complex (PIC), located in the highlands of Papua New Guinea (PNG). The highlands region marks the site of a Tertiary age continent-island-arc collision zone, located on the northeastern edge of the Australasian craton. The PIC was emplaced within continental crust near the Lagaip Fault Zone, which represents an Oligocene suture between the craton and volcano-sedimentary rocks of the Sepik terrane. Magmatism at Porgera probably occurred in response to the Late Miocene elimination of an oceanic microplate, and subsequent Early Pliocene collision between the craton margin and an arc system located on the Bismarck Sea plate. Gold mineralization occurred within 1 Ma of the time of magmatism. Metasomatism accompanying early disseminated Au mineralization in igneous host rocks resulted in additions of K, Rb, Mn, S, and CO 2, and depletions of Fe, Mg, Ca, Na, Ba, and Sr; rare-earth and high-field-strength elements remained largely immobile. Pervasive development of illite-K-feldspar-quartz-carbonate alteration assemblages suggests alteration by mildly acidic, 200 to 350°C fluids, at high water/ rock ratios. Strontium and lead isotopic compositions of minerals from early base-metal sulphide veins associated with K-metasomatism, and later quartz-roscoelite veins carrying abundant free gold and tellurides, are remarkably uniform (e.g., 87Sr /86Sr = 0.70745 ± 0.00044 [n = 10] , 207Pb /204Pb = 15.603 ± 0.004 [n = 15] ). These compositions fall between those of unaltered igneous and sedimentary host rocks, and specifically sedimentary rocks from the Jurassic Om Formation which underlies the deposit (igneous rocks: 87Sr /86Sr ≈ 0.7035 , 207Pb /204Pb ≈ 15.560 ; Om Formation: 87Sr /86Sr |t~ 0.7153 , 207Pb /204Pb ≈ 15.636 ). It is therefore suggested that the hydrothermal fluids acquired their Sr and Pb isotopic signatures by interaction with, or

  4. Influence of transient flow on the mobility of strontium in unsaturated sand column

    International Nuclear Information System (INIS)

    Mazet, P.

    2008-10-01

    The reactive transport of 85 Sr was studied on laboratory columns, focusing on the influence of transient unsaturated flow (cycles of infiltration and redistribution) associated with controlled geochemistry (constant concentrations of major elements and stable strontium in water). An original experimental tool (gamma attenuation system) allows us to follow at the same time the variations of humidity of the soil and the migration of radionuclide, in a non-destroying and definite way. First stage of this study concerned the implementation of the experimental tool to measure transient hydraulic events within the columns of sand. Several experiments of transport of 85 Sr were then performed with different water condition (saturated, unsaturated, permanent and transient flow). Experimental results were simulated using the computer codes HYDRUS-1D (phenomenological approach with partition coefficient K d ) and HYTEC (mechanistic geochemical/transport approach). Confrontation between experience and modelling shows that, for our operating conditions, transfer of 85 Sr can be predicted with an 'operational' approach using: 1) simplified geochemical model with partition coefficient K d concerning interactive reaction with the soil (K d value determined independently on saturated column, with the same water geochemistry), 2) permanent saturated (or unsaturated) flow, taking into account the cumulated infiltrated water during unsaturated transient hydraulic events concerning hydrodynamic. Generalization of these results (area of validity) suggests that the 'cumulated infiltrated water + K d ' approach can be use, for controlled water geochemistry, when the numerical value of K d is fairly strong (K d ≥≥1), and that it is insensitive to the value of the water content. Moreover, the presence of immobile water (∼10%) recorded with tritium transport, is undetectable with strontium. Explanation of this result is allocated to the different characteristic time residence

  5. Natural uranium and strontium isotope tracers of water sources and surface water-groundwater interactions in arid wetlands: Pahranagat Valley, Nevada, USA

    Science.gov (United States)

    Paces, James B.; Wurster, Frederic C.

    2014-01-01

    Near-surface physical and chemical process can strongly affect dissolved-ion concentrations and stable isotope compositions of water in wetland settings, especially under arid climate conditions. In contrast, heavy radiogenic isotopes of strontium (87Sr/86Sr) and uranium (234U/238U) remain largely unaffected and can be used to help identify unique signatures from different sources and quantify end-member mixing that would otherwise be difficult to determine. The utility of combined Sr and U isotopes are demonstrated in this study of wetland habitats on the Pahranagat National Wildlife Refuge, which depend on supply from large-volume springs north of the Refuge, and from small-volume springs and seeps within the Refuge. Water budgets from these sources have not been quantified previously. Evaporation, transpiration, seasonally variable surface flow, and water management practices complicate the use of conventional methods for determining source contributions and mixing relations. In contrast, 87Sr/86Sr and 234U/238U remain unfractionated under these conditions, and compositions at a given site remain constant. Differences in Sr- and U-isotopic signatures between individual sites can be related by simple two- or three-component mixing models. Results indicate that surface flow constituting the Refuge’s irrigation source consists of a 65:25:10 mixture of water from two distinct regionally sourced carbonate aquifer springs, and groundwater from locally sourced volcanic aquifers. Within the Refuge, contributions from the irrigation source and local groundwater are readily determined and depend on proximity to those sources as well as water management practices.

  6. Soil properties, strontium isotopic signatures and multi-element profiles to authenticate the origin of vegetables from small-scale regions: illustration with early potatoes from southern Italy.

    Science.gov (United States)

    Zampella, Mariavittoria; Quétel, Christophe R; Paredes, Eduardo; Goitom Asfaha, Daniel; Vingiani, Simona; Adamo, Paola

    2011-10-15

    We propose a method for the authentication of the origin of vegetables grown under similar weather conditions, in sites less than 10 km distance from the sea and distributed over a rather small scale area (58651 km(2)). We studied how the strontium (Sr) isotopic signature and selected elemental concentrations ([Mn], [Cu], [Zn], [Rb], [Sr] and [Cd]) in early potatoes from three neighbouring administrative regions in the south of Italy were related to the geological substrate (alluvial sediments, volcanic substrates and carbonate rocks) and to selected soil chemical properties influencing the bioavailability of elements in soils (pH, cation exchange capacity and total carbonate content). Through multiple-step multivariate statistics (PLS-DA) we could assign 26 potatoes (including two already commercialised samples) to their respective eight sites of production, corresponding to the first two types of geological substrates. The other 12 potatoes from four sites of production had similar characteristics in terms of the geological substrate (third type) and these soil properties could be grouped together. In this case, more discriminative parameters would be required to allow the differentiation between sites. The validation of our models included external prediction tests with data of potatoes harvested the year before and a study on the robustness of the uncertainties of the measurement results. Annual variations between multi-elemental and Sr isotopic fingerprints were observed in potatoes harvested from soils overlying carbonate rocks, stressing the importance of testing long term variations in authentication studies. Copyright © 2011 John Wiley & Sons, Ltd. and European Union [2011].

  7. A normalised seawater strontium isotope curve. Possible implications for Neoproterozoic-Cambrian weathering rates and the further oxygenation of the Earth

    International Nuclear Information System (INIS)

    Shields, G.A.

    2007-01-01

    The strontium isotope composition of seawater is strongly influenced on geological time scales by changes in the rates of continental weathering relative to ocean crust alteration. However, the potential of the seawater 87 Sr/ 86 Sr curve to trace globally integrated chemical weathering rates has not been fully realised because ocean 87 Sr/ 86 Sr is also influenced by the isotopic evolution of Sr sources to the ocean. A preliminary attempt is made here to normalise the seawater 87 Sr/ 86 Sr curve to plausible trends in the 87 Sr/ 86 Sr ratios of the three major Sr sources: carbonate dissolution, silicate weathering and submarine hydrothermal exchange. The normalised curve highlights the Neoproterozoic-Phanerozoic transition as a period of exceptionally high continental influence, indicating that this interval was characterised by a transient increase in global weathering rates and/or by the weathering of unusually radiogenic crustal rocks. Close correlation between the normalised 87 Sr/ 86 Sr curve, a published seawater δ 34 S curve and atmospheric pCO 2 models is used here to argue that elevated chemical weathering rates were a major contributing factor to the steep rise in seawater 87 Sr/ 86 Sr from 650 Ma to 500 Ma. Elevated weathering rates during the Neoproterozoic-Cambrian interval led to increased nutrient availability, organic burial and to the further oxygenation of Earth's surface environment. Use of normalised seawater 87 Sr/ 86 Sr curves will, it is hoped, help to improve future geochemical models of Earth System dynamics. (orig.)

  8. The strontium isotopic composition of interstitial waters from sites 245 and 336 of the deep sea drilling project

    International Nuclear Information System (INIS)

    Hawkesworth, C.J.; Elderfield, H.

    1978-01-01

    Measurements of 87 Sr/ 86 Sr ratios of interstitial waters from leg 25, site 245 and leg 38, site 336 of the Deep Sea Drilling Project show that the enrichment of Sr 2+ with depth is caused both by the alteration of volcanic material and by the introduction of strontium derived from calcium carbonate. 87 Sr/ 86 Sr ratios range from 0.70913 to 0.70794 at site 245 and from 0.70916 to 0.70694 at site 336. The low ratios compared with contemporaneous seawater reflect the release of Sr from a volcanic source having, according to material-balance calculations, a 87 Se/ 86 Sr ratio of about 0.7034 at site 336. At this site the source appears to be volcanic ash and not basaltic basement which acts as a sink for Sr 2+ during in situ low-temperature weathering. The volcanic contribution to the strontium enrichment in the basal interstitial waters varies from 50% at site 336. The remaining Sr 2+ is derived from Sr-rich biogenic carbonate during diagenetic recrystallization to form Sr-poor calcite. (Auth.)

  9. Lead-strontium isotopic variations along the East Pacific Rise and the Mid-Atlantic Ridge: A comparative study

    International Nuclear Information System (INIS)

    Hamelin, B.; Dupre, B.; Allegre, C.J.

    1984-01-01

    We have determined the Pb and Sr isotopic compositions in a number of fresh young oceanic basalts from the East Pacific Rise (between 20 0 N and 21 0 S latitudes), and from the Mid-Atlantic Ridge (between 65 0 N and 10 0 N). A comparison between the Atlantic and Pacific results reveals that there is a wider range of values for the Atlantic than for the Pacific. After filtering the short wavelengths, a good correlation is obtained between long-wavelength bathymetric and isotopic variations for the Atlantic. The preferred model proposed to explain these differences involves the constant presence of hot spots under ridges. On slow-spreading ridges like the Atlantic, the host spots signature is clearly visible in both bathymetry and isotopic ratios. On fast-spreading centres, the hot spot signature in both the bathymetry and isotopic signature may be diluted by the rapid supply of material coming from the asthenosphere. However, an alternative explanation for which no hot spot influence is found on the East Pacific Rise cannot be definitely ruled out. In two occurrences, south of the Hayes fracture zone (Atlantic), large isotopic heterogeneities are observed within a single dredge. This does not contradict the concept of regional isotopic regularities, but suggests that blob injection and source mixing may be observed at very different scales under the ridges. (orig./WB)

  10. Adaptation of the ICRP models for the Techa River populations to estimate in utero and postnatal haemopoietic tissue doses from ingested strontium isotopes

    International Nuclear Information System (INIS)

    Shagina, Natalia; Tolstykh, Evgenia; Degteva, Marina; Fell, Tim; Harrison, John

    2008-01-01

    Full text: Reliable estimation of tissue doses for exposed individuals is very important in epidemiological studies. Long-term cohort studies of the Techa River populations exposed in the early 1950s due to releases of liquid radioactive wastes from the Mayak plutonium production facility (Southern Urals, Russia) are unique in allowing the quantification of risks from low-level chronic exposure of the general population and providing information on risks for persons exposed in utero. Strontium isotopes were the most important contributors to haemopoietic tissue doses for people living in the riverside settlements. Large-scale monitoring of the exposed population has provided a comprehensive database, including post mortem and in vivo measurements of 90 Sr in bones and whole body, for use in the estimation of doses. The International Commission on Radiological Protection (ICRP) has published biokinetic and dosimetric models for the calculation of doses to members of the public, including doses from in utero exposures and from intakes with breast milk. However, the ICRP models as applied to Sr required modification to provide best estimates of doses to Techa River residents. Adaptations were made to the ICRP model for Sr in children and adults to take account of population-specific features relating to bone mineral turnover and to model age and gender differences in strontium retention. Refinements in the ICRP model for Sr uptake and retention in the fetus were made to improve the treatment of discrimination against Sr, relative to Ca, in transfer from maternal to foetal blood and to take account of population-specific data on the calcium content of the maternal and fetal skeleton. Modification of the ICRP model for Sr transfer in breast-milk included adaptations relating to changes in maternal mineral metabolism during lactation and consideration of population-specific features of breast feeding in the rural population. The improved models were successfully

  11. High-Throughput Method for Strontium Isotope Analysis by Multi-Collector-Inductively Coupled Plasma-Mass Spectrometer

    Energy Technology Data Exchange (ETDEWEB)

    Wall, Andrew J. [National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States); Capo, Rosemary C. [Univ. of Pittsburgh, PA (United States); Stewart, Brian W. [Univ. of Pittsburgh, PA (United States); Phan, Thai T. [Univ. of Pittsburgh, PA (United States); Jain, Jinesh C. [National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States); Hakala, Alexandra [National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States); Guthrie, George D. [National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States)

    2016-09-22

    This technical report presents the details of the Sr column configuration and the high-throughput Sr separation protocol. Data showing the performance of the method as well as the best practices for optimizing Sr isotope analysis by MC-ICP-MS is presented. Lastly, this report offers tools for data handling and data reduction of Sr isotope results from the Thermo Scientific Neptune software to assist in data quality assurance, which help avoid issues of data glut associated with high sample throughput rapid analysis.

  12. High-Throughput Method for Strontium Isotope Analysis by Multi-Collector-Inductively Coupled Plasma-Mass Spectrometer

    Energy Technology Data Exchange (ETDEWEB)

    Hakala, Jacqueline Alexandra [National Energy Technology Lab. (NETL), Morgantown, WV (United States)

    2016-11-22

    This technical report presents the details of the Sr column configuration and the high-throughput Sr separation protocol. Data showing the performance of the method as well as the best practices for optimizing Sr isotope analysis by MC-ICP-MS is presented. Lastly, this report offers tools for data handling and data reduction of Sr isotope results from the Thermo Scientific Neptune software to assist in data quality assurance, which help avoid issues of data glut associated with high sample throughput rapid analysis.

  13. Strontium isotope ratios - a possible tool to study the authenticity of Indian tea using MC-ICP-MS

    International Nuclear Information System (INIS)

    Lagad, Rupali A.; Alamelu, D.; Aggarwal, Suresh K.; Singh, Sunil K.

    2011-01-01

    In the present study, an analytical procedure based on determination of the Sr isotope ratio 87 Sr/ 86 Sr in the Indian tea samples by MC-ICP-MS was developed and applied to 28 tea samples from four different Indian regions. The 87 Sr/ 86 Sr 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 87 Sr/ 86 Sr atom ratio follows the order Darjeeling > Kangra > Assam > Munnar

  14. Isotope hydrology and baseflow geochemistry in natural and human-altered watersheds in the Inland Pacific Northwest, USA

    Science.gov (United States)

    Ricardo Sanchez-Murillo; Erin S. Brooks; William J. Elliot; Jan Boll

    2015-01-01

    This study presents a stable isotope hydrology and geochemical analysis in the inland Pacific Northwest (PNW) of the USA. Isotope ratios were used to estimate mean transit times (MTTs) in natural and human-altered watersheds using the FLOWPC program. Isotope ratios in precipitation resulted in a regional meteoric water line of ä2H = 7.42·ä18O + 0.88 (n = 316; r2 = 0.97...

  15. Provenancing of unidentified World War II casualties: Application of strontium and oxygen isotope analysis in tooth enamel.

    Science.gov (United States)

    Font, Laura; Jonker, Geert; van Aalderen, Patric A; Schiltmans, Els F; Davies, Gareth R

    2015-01-01

    In 2010 and 2012 two sets of unidentified human remains of two World War II soldiers were recovered in the area where the 1944-1945 Kapelsche Veer bridgehead battle took place in The Netherlands. Soldiers of four Allied nations: British Royal Marine Commandos, Free Norwegian Commandos, Free Poles and Canadians, fought against the German Army in this battle. The identification of these two casualties could not be achieved using dental record information of DNA analysis. The dental records of Missing in Action soldiers of the Allied nations did not match with the dental records of the two casualties. A DNA profile was determined for the casualty found in 2010, but no match was found. Due to the lack of information on the identification of the casualties provided by routine methods, an isotope study was conducted in teeth from the soldiers to constrain their provenance. The isotope study concluded that the tooth enamel isotope composition for both casualties matched with an origin from the United Kingdom. For one of the casualties a probable origin from the United Kingdom was confirmed, after the isotope study was conducted, by the recognition of a characteristic belt buckle derived from a Royal Marine money belt, only issued to British Royal Marines, found with the remains of the soldier. Copyright © 2014 Forensic Science Society. Published by Elsevier Ireland Ltd. All rights reserved.

  16. Strontium and neodymium isotopic evidence for the heterogeneous nature and development of the mantle beneath Afar (Ethiopia)

    International Nuclear Information System (INIS)

    Betton, P.J.; Civetta, L.

    1984-01-01

    Neodymium isotope and REE analyses of recent volcanic rocks and spinel lherzolite nodules from the Afar area are reported. The 143 Nd/ 144 Nd ratios of the volcanic rocks range from 0.51286 to 0.51304, similar to the range recorded from Iceland. However, the 87 Sr/ 86 Sr ratios display a distinctly greater range (0.70328-0.70410) than those reported from the primitive rocks of Iceland. Whole rock samples and mineral separates from the spinel lherzolite nodules exhibit uniform 143 Nd/ 144 Nd ratios (ca. 0.5129) but varied 87 Sr/ 86 Sr ratios in the range 0.70427-0.70528. The Sr-Nd isotope variations suggest that the volcanic rocks may have been produced by mixing between two reservoirs with distinct isotopic compositions. Two possible magma reservoirs in this area are the source which produced the 'MORB-type' volcanics in the Red Sea and Gulf of Aden and the anomalous source represented by the nodule suite. The isotopic composition of the volcanics is compatible with mixing between these two reservoirs. It is shown that the anomalous source with a high 87 Sr/ 86 Sr ratio cannot have been produced by simple processes of partial melting and mixing within normal mantle. Instead the high 87 Sr/ 86 Sr is equated with a fluid phase. A primitive cognate fluid, subducted seawater or altered oceanic lithosphere may have been responsible for the generation of the source with a high 87 Sr/ 86 Sr ratio. (orig.)

  17. 230Th-238U radioactive disequilibria in tholeiites from the FAMOUS zone (Mid-Atlantic Ridge, 36050'N): Th and Sr isotopic geochemistry

    International Nuclear Information System (INIS)

    Condomines, M.; Morand, P.; Allegre, C.J.

    1981-01-01

    We analyzed, U, Th and 230 Th/ 232 Th activity ratios for a few tholeiites from the Mid-Atlantic Ridge FAMOUS zone at 36 0 50'N. The results show a fairly wider scatter for both Th/U and ( 230 Th/ 232 Th) ratios. Seawater contamination appears to be responsible for this scatter and, for the uranium, produces an increase in content yielding a ( 234 U/ 238 U) ratio greater than 1 and, for the Th, an increase of the ( 230 Th/ 232 Th) ratio which is a very sensitive indicator for contamination. Also, the latter often is selective: U, Th and Sr are not affected in the same manner. When discarding all data for contaminated samples, the FAMOUS zone appears to be very homogeneous with a Th/U ratio value of 3.05 and a ( 230 Th/ 232 Th) ratio value of 1.24. Comparison with other active volcanic areas reveals a negative correlation between ( 230 Th/ 232 Th) and 87 Sr/ 86 Sr ratios for present lavas which is indicative of a consistency in Th-U and Rb-Sr fractionation in the source regions of these magmas. The Th isotopic geochemistry can thus provide useful information for the study of present volcanism, information as valuable as that from Sr, Pb or Nd isotopes. (orig.)

  18. Geology and stable isotope geochemistry of Paleoarchean sulfur. Formation, preservation and geobiology of ancient pyrite and barite

    NARCIS (Netherlands)

    Roerdink, D.L.|info:eu-repo/dai/nl/318834340

    2013-01-01

    Sulfur isotopes in ancient sulfate and sulfide minerals provide a comprehensive record of microbial processes involved in the early sulfur cycle on Earth. However, the interpretation of these isotopic signatures requires information on the geological context of such samples, because abiotic

  19. 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

  20. Paleoenvironmental conditions and strontium isotope stratigraphy in the Paleogene Gafsa Basin (Tunisia) deduced from geochemical analyses of phosphatic fossils

    Science.gov (United States)

    Kocsis, László; Ounis, Anouar; Chaabani, Fredj; Salah, Neili Mohamed

    2013-06-01

    Fossil shark teeth and coprolites from three major phosphorite occurrences in the Gafsa Basin (southwestern Tunisia) were investigated for their geochemical compositions to improve local stratigraphy and to better assess paleoenvironmental conditions. 87Sr/86Sr isotope ratios of shark teeth from the Early Maastrichtian El Haria Formation and from the Early Eocene Métlaoui s.s. Formation yielded Sr isotope ages of 68 ± 1 and 47.9 ± 1.3 Ma, respectively, which accord with the expected stratigraphic positions of these sediments. Conversely, shark teeth from the Paleocene-Eocene Chouabine Formation have large variation in Sr isotope ratios even within individual layers. After statistical treatment and then elimination of certain outlier samples, three age-models are proposed and discussed. The most reasonable solution includes three subsequent Sr ages of 61.8 ± 2.2 Ma, 57.2 ± 1.8 and 54.6 ± 1.6 for layer IX, layers VIII-V and layers IV-0, respectively. Three scenarios are discussed for explanation of the presence of the outliers: (1) diagenesis, (2) re-working and (3) locally controlled seawater Sr isotope ratio. The most plausible account for the higher 87Sr/86Sr ratios relative to the global ocean in some fossils is enhanced intrabasinal re-working due to low sea level. Conversely, the sample with lower 87Sr/86Sr than the global seawater may link to diagenesis or to seawater influenced by weathering of Late Cretaceous marine carbonates, which latter is supported by model calculation as well. The ɛNd values of these fossils are very similar to those reported for Paleogene and Late Cretaceous Tethyan seawater and are compatible with the above interpretations. The relatively low oxygen isotope values in shark teeth from the topmost phosphate bed of the Chouabine Formation, together with the Sr isotope results, point toward recovering better connections with the open sea. These δ18O data reflect elevated ambient temperature, which may link to the Early Eocene

  1. Strontium isotopes test long-term zonal isolation of injected and Marcellus formation water after hydraulic fracturing.

    Science.gov (United States)

    Kohl, Courtney A Kolesar; Capo, Rosemary C; Stewart, Brian W; Wall, Andrew J; Schroeder, Karl T; Hammack, Richard W; Guthrie, George D

    2014-08-19

    One concern regarding unconventional hydrocarbon production from organic-rich shale is that hydraulic fracture stimulation could create pathways that allow injected fluids and deep brines from the target formation or adjacent units to migrate upward into shallow drinking water aquifers. This study presents Sr isotope and geochemical data from a well-constrained site in Greene County, Pennsylvania, in which samples were collected before and after hydraulic fracturing of the Middle Devonian Marcellus Shale. Results spanning a 15-month period indicated no significant migration of Marcellus-derived fluids into Upper Devonian/Lower Mississippian units located 900-1200 m above the lateral Marcellus boreholes or into groundwater sampled at a spring near the site. Monitoring the Sr isotope ratio of water from legacy oil and gas wells or drinking water wells can provide a sensitive early warning of upward brine migration for many years after well stimulation.

  2. 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.

  3. High-resolution C and O stable isotope geochemistry of the early Aptian OAE1a at Cau (Prebetic Zone, Spain): Preliminary results from sediment core.

    Science.gov (United States)

    Alejandro Ruiz-Ortiz, Pedro; Aguado, Roque; Castro, José Manuel; Gallego, David; de Gea, Ginés Alfonso; Jarvis, Ian; Molina, José Miguel; Nieto, Luis Miguel; Pancost, Richard; Quijano, María Luisa; Reolid, Matías; Rodriguez, Rafael; Skelton, Peter; Weisser, Helmut

    2017-04-01

    The occurrence of time intervals of enhanced deposition of organic matter (OM) during the Cretaceous, defined as Oceanic Anoxic Events (OAE), reflect abrupt changes in global carbon cycling. The Aptian OAE1a (120 Ma), represents an excellent example, recorded in all the main ocean basins, associated to massive burial of organic matter in marine sediments [1]. Much research has been done on the OAE1a from different sections in the world over the last decades, including the definition of the C-isotope stratigraphy of the event [2]. Notwithstanding, higher-resolution studies across the entire event will be crucial to shed light into the precise timing and rates of the different environmental and biotic changes that occurred. The Cau section is located in the easternmost part of the Prebetic Zone (Betic Cordillera), which represents the platform deposits of the Southern Iberian palaeomargin. The Lower Aptian of the Cau section is represented by a hemipelagic unit (Almadich Formation, ca. 200 m thick), deposited in a highly subsiding sector of a tilted block, located in the distal parts of the Prebetic Platform. Previous studies of the Lower Aptian of the Cau section have focused on the stratigraphy, bioevents, C-isotope stratigraphy, and organic and elemental geochemistry [3], [4], and in the reconstruction of pCO2 from organic geochemistry proxies [5]. All these studies reveal that the Cau section represents an excellent site to investigate the OAE 1a, based on its unusual high thickness and stratigraphic continuity, the quality and preservation of fossils and the geochemical signatures. Here we present the first results of a high-resolution carbonate C-isotope study based on the the analysis of three new research cores drilled at Cau in autumn 2015 [6]. These new data represent an important advance in the knowledge of the C-isotope record of the OAE 1a, presenting a more continuous record at a higher resolution than previous studies. This leads to the refining of the

  4. Strontium and neodymium isotopic evidence for the heterogeneous nature and development of the mantle beneath Afar (Ethiopia)

    Energy Technology Data Exchange (ETDEWEB)

    Betton, P.J. (Leeds Univ. (UK). Dept. of Earth Sciences); Civetta, L. (Naples Univ. (Italy). Dipartimento di Geofisica e Vulcanologia)

    1984-11-01

    Neodymium isotope and REE analyses of recent volcanic rocks and spinel lherzolite nodules from the Afar area are reported. The /sup 143/Nd//sup 144/Nd ratios of the volcanic rocks range from 0.51286 to 0.51304, similar to the range recorded from Iceland. However, the /sup 87/Sr//sup 86/Sr ratios display a distinctly greater range (0.70328-0.70410) than those reported from the primitive rocks of Iceland. Whole rock samples and mineral separates from the spinel lherzolite nodules exhibit uniform /sup 143/Nd//sup 144/Nd ratios (ca. 0.5129) but varied /sup 87/Sr//sup 86/Sr ratios in the range 0.70427-0.70528. The Sr-Nd isotope variations suggest that the volcanic rocks may have been produced by mixing between two reservoirs with distinct isotopic compositions. Two possible magma reservoirs in this area are the source which produced the 'MORB-type' volcanics in the Red Sea and Gulf of Aden and the anomalous source represented by the nodule suite. The isotopic composition of the volcanics is compatible with mixing between these two reservoirs. It is shown that the anomalous source with a high /sup 87/Sr//sup 86/Sr ratio cannot have been produced by simple processes of partial melting and mixing within normal mantle. Instead the high /sup 87/Sr//sup 86/Sr is equated with a fluid phase. A primitive cognate fluid, subducted seawater or altered oceanic lithosphere may have been responsible for the generation of the source with a high /sup 87/Sr//sup 86/Sr ratio.

  5. Si-metasomatism in serpentinized peridotite: The effects of talc-alteration on strontium and boron isotopes in abyssal serpentinites from Hole 1268a, ODP Leg 209

    Science.gov (United States)

    Harvey, Jason; Savov, Ivan P.; Agostini, Samuele; Cliff, Robert A.; Walshaw, Richard

    2014-02-01

    Ultramafic rocks recovered from Hole 1268a, Ocean Drilling Program Leg 209, to the south of the 15°20‧N Fracture Zone on the Mid-Atlantic ridge have experienced a complex history of melt depletion and subsequent interaction with a series of fluids under varying temperature and pH conditions. After intense melt depletion, varying degrees of serpentinization at 100-200 °C took place, initially under seawater-like pH conditions. Subsequently, interaction with a higher temperature (300-350 °C) fluid with low (4-5) pH and low MgO/SiO2 resulted in the heterogeneous alteration of these serpentinites to talc-bearing ultramafic lithologies. The proximity of the currently active, high temperature Logatchev hydrothermal field, located on the opposite flank of the Mid-Atlantic ridge, suggests that unlike more distal localities sampled during ODP Leg 209, Hole 1268a has experienced Si-metasomatism (i.e. talc-alteration) by a Logatchev-like hydrothermal fluid. Serpentinite strontium isotope ratios were not materially shifted by interaction with the subsequent high-T fluid, despite the likelihood that this fluid had locally interacted with mid-ocean ridge gabbro. 87Sr/86Sr in the ultramafic lithologies of Hole 1268a are close to that of seawater (c.0.709) and even acid leached serpentinites retain 87Sr/86Sr in excess of 0.707, indistinguishable from Logatchev hydrothermal fluid. On the other hand, boron isotope ratios appear to have been shifted from seawater-like values in the serpentinites (δ11B = c.+40‰) to much lighter values in talc-altered serpentinites (δ11B = +9 to +20‰). This is likely a consequence of the effects of changing ambient pH and temperature during the mineralogical transition from serpentine to talc. Heterogeneous boron isotope systematics have consequences for the composition of ultramafic portions of the lithosphere returned to the convecting mantle by subduction. Inhomogeneities in δ11B, [B] and mineralogy introduce significant uncertainties in

  6. Estimating westslope cutthroat trout (Oncorhynchus clarkii lewisi) movements in a river network using strontium isoscapes

    Science.gov (United States)

    Muhlfeld, Clint C.; Simon R. Thorrold,; Thomas E. McMahon,; Marotz, Brian

    2012-01-01

    We used natural variation in the strontium concentration (Sr:Ca) and isotope composition (87Sr:86Sr) of stream waters and corresponding values recorded in otoliths of westslope cutthroat trout (Oncorhynchus clarkii lewisi) to examine movements during their life history in a large river network. We found significant spatial differences in Sr:Ca and 87Sr:86Sr values (strontium isoscapes) within and among numerous spawning and rearing streams that remained relatively constant seasonally. Both Sr:Ca and 87Sr:86Sr values in the otoliths of juveniles collected from nine natal streams were highly correlated with those values in the ambient water. Strontium isoscapes measured along the axis of otolith growth revealed that almost half of the juveniles had moved at least some distance from their natal streams. Finally, otolith Sr profiles from three spawning adults confirmed homing to natal streams and use of nonoverlapping habitats over their migratory lifetimes. Our study demonstrates that otolith geochemistry records movements of cutthroat trout through Sr isoscapes and therefore provides a method that complements and extends the utility of conventional tagging techniques in understanding life history strategies and conservation needs of freshwater fishes in river networks.

  7. Investigation of Chemical and Physical Changes to Bioapatite During Fossilization Using Trace Element Geochemistry, Infrared Spectroscopy and Stable Isotopes

    Science.gov (United States)

    Suarez, C. A.; Kohn, M. J.

    2013-12-01

    Bioapatite in the form of vertebrate bone can be used for a wide variety of paleo-proxies, from determination of ancient diet to the isotopic composition of meteoric water. Bioapatite alteration during diagenesis is a constant barrier to the use of fossil bone as a paleo-proxy. To elucidate the physical and chemical alteration of bone apatite during fossilization, we analyzed an assortment of fossil bones of different ages for trace elements, using LA-ICP-MS, stable isotopes, and reflected IR spectroscopy. One set of fossil bones from the Pleistocene of Idaho show a diffusion recrystallization profile, however, rare earth element (REE) profiles indicate diffusion adsorption. This suggests that REE diffusion is controlled by changing (namely decreasing) boundary conditions (i.e. decreasing concentration of REE in surrounding pore fluids). Reflected IR analysis along this concentration profile reveal that areas high in U have lost type A carbonate from the crystal structure in addition to water and organics. Stable isotopic analysis of carbon and oxygen will determine what, if any, change in the isotopic composition of the carbonate component of apatite has occurred do to the diffusion and recrystallization process. Analysis of much older bone from the Cretaceous of China reveal shallow REE and U concentration profiles and very uniform reflected IR spectra with a significant loss of type A carbonate throughout the entire bone cortex. Analysis of stable isotopes through the bone cortex will be compared to the stable isotopes collected from the Pleistocene of Idaho.

  8. A study on the variation of strontium isotopic ratio in Darjeeling tea using MC-ICP-MS

    International Nuclear Information System (INIS)

    Lagad, Rupali A.; Alamelu, D.; Jagadish Kumar, S.; Aggarwal, Suresh K.; Rai, Vinai; Singh, S.K.

    2011-01-01

    In the present study, an analytical procedure based on the determination of the Sr isotope ratio 87 Sr/ 86 Sr in the Darjeeling tea samples by MC-ICP-MS was developed and applied to 15 green tea samples obtained from different tea gardens in Darjeeling. Variation in 87 Sr/ 86 Sr ratio was observed among eleven different tea gardens fro different geographical locations. The obtained data on 87 Sr/ 86 Sr ration in authentic tea leaves samples can be useful while comparing it with processed tea samples from respective regions

  9. The geographic distribution of strontium isotopes in Danish surface waters - A base for provenance studies in archaeology, hydrology and agriculture

    DEFF Research Database (Denmark)

    Frei, Karin Margarita; Frei, Robert

    2011-01-01

    is consequently not readily transferred into the shallow-rooting plants and into small herbivores feeding on them. Since drinking water is a likely important source of Sr uptake of humans and larger animals, the contention is that a surface water isotopic composition can potentially characterize the bio...... some notable exceptions) neither mirror the pre-Quarternary bedrock geology nor a (Pleistocene) soil-type distribution map of Denmark. As a conservative suggestion, the use of the average 87Sr/86Sr ratio of 0.7096 ± 0.0015 (2r) is recommended as an average for bio-available Sr from within Denmark...

  10. The radiogenic and stable Sr isotope geochemistry of basalt weathering in Iceland: Role of hydrothermal calcite and implications for long-term climate regulation

    Science.gov (United States)

    Andrews, M. Grace; Jacobson, Andrew D.

    2017-10-01

    Several studies have examined the geochemistry of Icelandic rivers to quantify the relationship between basalt weathering and long-term climate regulation. Recent research has suggested that the chemical weathering of hydrothermal and metamorphic calcite contributes significant quantities of HCO3- to the Icelandic riverine flux (Jacobson et al., 2015). Because the HCO3- derives from volcanic CO2 that was sequestered in mineral form prior to atmospheric injection, the strength of the basalt weathering feedback occurring in Iceland may be lower than previously realized. To test these hypotheses, we analyzed the radiogenic and stable Sr isotope composition (87Sr/86Sr and δ88/86Sr) of the same suite of water, rock, and mineral samples as examined in Jacobson et al. (2015), and we developed a simple model of the long-term C cycle that considers the transformation of volcanic CO2 to HCO3- during subsurface silicate weathering, which is a precursor to hydrothermal calcite formation. Interpretations based on 87Sr/86Sr and Ca/Sr ratios suggest that conservative, three-component mixing between basalt, calcite, and atmospheric deposition adequately explains river geochemistry. On average, the δ88/86Sr values of glacial and non-glacial rivers (0.414‰ and 0.388‰, respectively) are generally higher than those for basalt (0.276‰); however, calcite δ88/86Sr values (0.347‰) are also higher than those for basalt and span the range of riverine values. Thus, riverine δ88/86Sr values are also consistent three-component mixing between basalt, calcite, and atmospheric deposition. Isotopic fractionation is not required to explain riverine trends. Finally, model equations for the long-term C cycle demonstrate that subsurface silicate weathering reduces the magnitude of the volcanic CO2 degassing flux, which in turn causes the atmosphere to stabilize at lower pCO2 values compared to the case where no subsurface silicate weathering occurs. However, the proportion of the net

  11. Simulating the Transfer of Strontium-90 from Soil to Leafy Vegetables by Using Strontium-88.

    Science.gov (United States)

    Kuke, Ding; Shujuan, Liu; Yingxue, He; Dong, Yan; Fengshou, Zhang; Shuifeng, Wang; Jinghua, Guo; Wei, Zhang; Xin, Wang; Xiaoyan, Jiang

    The transfer, from soil to Chinese cabbage and spinach, of radioactive strontium-90 released as a result of accidents in nuclear power stations was studied using a stable isotope of strontium, namely nuclide strontium-88 ( 88 Sr). The study led to an experimental model for assessing the hazard of radionuclide strontium-90 ( 90 Sr) entering the food chain and for predicting the risk to food safety. Chinese cabbage and spinach were grown in pots in a greenhouse and irrigated with deionized water containing known quantities of strontium. Based on the strontium content of that water, the plants were divided into five groups (treatments) and strontium content of the soil, and 30-day-old plants were determined by inductively coupled plasma atomic emission spectroscopy instrument (ICP-AES). Data on the strontium content of soil and plants enabled the development of a model using MATLAB, a mathematical software package, which included curve fitting and problem solving using regression equations and differential equations. Although strontium curves for leaves, stems, and roots of Chinese cabbage were not exactly the same, all showed a non-linear increase when compared with the increase in the content of strontium in soil. Strontium curves for leaves, stems, and roots of spinach were very similar and showed an initial increase followed by a decrease. Strontium concentrations in both Chinese cabbage and spinach were initially related to the concentrations of sodium and sulfur, the next two relevant nuclides being calcium and magnesium. The relationship between calcium and strontium in Chinese cabbage was different from that in spinach. By using 88 Sr to simulate the transfer of radionuclide 90 Sr from soil to a crop, the relevant data required to deal with accidental release of strontium can be obtained using a fitting curve and regression equations, thereby providing some experimental basis for evaluating the potential hazards posed by such accidents to the food chain.

  12. Fit for purpose validated method for the determination of the strontium isotopic signature in mineral water samples by multi-collector inductively coupled plasma mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Brach-Papa, Christophe; Van Bocxstaele, Marleen; Ponzevera, Emmanuel [European Commission - Joint Research Centre - Institute for Reference Materials and Measurements, Retieseweg 111 - 2440 Geel (Belgium); Quetel, Christophe R. [European Commission - Joint Research Centre - Institute for Reference Materials and Measurements, Retieseweg 111 - 2440 Geel (Belgium)], E-mail: christophe.quetel@ec.europa.eu

    2009-03-15

    A robust method allowing the routine determination of n({sup 87}Sr)/n({sup 86}Sr) with at least five significant decimal digits for large sets of mineral water samples is described. It is based on 2 consecutive chromatographic separations of Sr associated to multi-collector inductively coupled plasma mass spectrometry (MC-ICPMS) measurements. Separations are performed using commercial pre-packed columns filled with 'Sr resin' to overcome isobaric interferences affecting the determination of strontium isotope ratios. The careful method validation scheme applied is described. It included investigations on all parameters influencing both chromatographic separations and MC-ICPMS measurements, and also the test on a synthetic sample made of an aliquot of the NIST SRM 987 certified reference material dispersed in a saline matrix to mimic complex samples. Correction for mass discrimination was done internally using the n({sup 88}Sr)/n({sup 86}Sr) ratio. For comparing mineral waters originating from different geological backgrounds or identifying counterfeits, calculations involved the well known consensus value (1/0.1194) {+-} 0 as reference. The typical uncertainty budget estimated for these results was 40 'ppm' relative (k = 2). It increased to 150 'ppm' (k = 2) for the establishment of stand alone results, taking into account a relative difference of about 126 'ppm' systematically observed between measured and certified values of the NIST SRM 987. In case there was suspicion of a deviation of the n({sup 88}Sr)/n({sup 86}Sr) ratio (worst case scenario) our proposal was to use the NIST SRM 987 value 8.37861 {+-} 0.00325 (k = 2) as reference, and assign a typical relative uncertainty budget of 300 'ppm' (k = 2). This method is thus fit for purpose and was applied to eleven French samples.

  13. Gamow-Teller decay and nuclear deformation: implementing of a new total absorption spectrometer, study of isotopes N ≅ Z krypton and strontium

    International Nuclear Information System (INIS)

    Poirier, E.

    2002-12-01

    Nuclei with A ∼ 70 along the N=Z line are known to be the scene of phenomena closely related to the nuclear deformation and are of particular interest since theoretical mean field calculations predict that a large part of the Gamow-Teller resonance might be located below the ground state of the mother nucleus and then be accessible through β-decay studies. These results have shown the effect of the shape of the ground state on the intensity of the Gamow-Teller strength. Thus, the experimental determination, through δ-decay, of the Gamow-Teller strength distribution and the comparison to the theoretical predictions allow to pin down the quadrupolar deformation parameter of the ground state of the parent nucleus. In order to study the neutron deficient isotopes of krypton (A=72,73,74,75) and strontium (A=76,77,78) and to establish the β-strength on the full energy range, a new total absorption spectrometer (TAgS) has been built in the frame of an international collaboration and installed at the (SOLDE/CERN mass separator. For the data analysis, the response function R of the spectrometer has been calculated by means of Monte-Carlo simulations, based on the GEANT4 code, and of a statistical description of the level scheme in the daughter nucleus. The β-feeding distribution has been obtained from experimental spectra through a method based on Bayes theorem and then converted into Gamow-Teller strength. The results coming from the 74 Kr decay analysis allow to describe the ground state of such a nucleus as the coexistence of an oblate shape and of a prolate shape. In the case of 76 Sr, the experimental Gamow-Teller strength distribution strongly indicates a prolate deformation. (author)

  14. Isotope hydrology and baseflow geochemistry in natural and human-altered watersheds in the Inland Pacific Northwest, USA.

    Science.gov (United States)

    Sánchez-Murillo, Ricardo; Brooks, Erin S; Elliot, William J; Boll, Jan

    2015-01-01

    This study presents a stable isotope hydrology and geochemical analysis in the inland Pacific Northwest (PNW) of the USA. Isotope ratios were used to estimate mean transit times (MTTs) in natural and human-altered watersheds using the FLOWPC program. Isotope ratios in precipitation resulted in a regional meteoric water line of δ(2)H = 7.42·δ(18)O + 0.88 (n = 316; r(2) = 0.97). Isotope compositions exhibited a strong temperature-dependent seasonality. Despite this seasonal variation, the stream δ(18)O variation was small. A significant regression (τ = 0.11D(-1.09); r(2) = 0.83) between baseflow MTTs and the damping ratio was found. Baseflow MTTs ranged from 0.4 to 0.6 years (human-altered), 0.7 to 1.7 years (mining-altered), and 0.7 to 3.2 years (forested). Greater MTTs were represented by more homogenous aqueous chemistry whereas smaller MTTs resulted in more dynamic compositions. The isotope and geochemical data presented provide a baseline for future hydrological modelling in the inland PNW.

  15. Integration of inorganic and isotopic geochemistry with endocrine disruption activity assays to assess risks to water resources near unconventional oil and gas development in Garfield County, CO.

    Science.gov (United States)

    Harkness, J.; Kassotis, C.; Cornelius, J.; Nagel, S.; Vengosh, A.

    2016-12-01

    The rise of hydraulic fracturing in the United States has sparked a debate about the impact of oil and gas development on the quality of water resources. Wastewater associated with hydraulic fracturing includes injection fluid that is a mixture of sand, freshwater and synthetic organic chemicals, flowback water that is a mixture of injection fluid and formation brine, and produced water that is primarily brine. The fluids range in salinity and chemical composition that can have different environmental impacts. We analyzed the inorganic and isotope geochemistry of 58 surface and groundwater samples near and away from unconventional oil and gas operations (UOG), along with hormonal profiles via bioassays. Cl (0.12 to 198 mg/L), Na (1.2 to 518 mg/L) and Sr (1.4 to 2410 ug/L) were higher in both groundwater and surface water near UOG wells. Four surface waters and one groundwater had Br/Cl indicative of brine contamination (>1.5x10-3). Three of the SW samples also had 87Sr/86Sr ratios similar to values found in produced or flowback water (0.7118 and 0.7158, respectively) from the Williams-Fork formation and elevated compared to background ratios (0.71062 to 0.7115). Increased progestogenic activity was observed in groundwater near UOG operations and inncreased estrogenic, androgenic, progestogenic, anti-androgenic, anti-progestogenic, and anti-glucocorticoid activities in surface water near UOG operations. The association of increased EDCs with inorganic and isotopic indicators of UOG wastewater provides evidence for possible environmental and health impacts from drilling activity.

  16. Geochemistry and oxygen isotope composition of main-group pallasites and olivine-rich clasts in mesosiderites

    DEFF Research Database (Denmark)

    Greenwood, Richard C.; Barrat, Jean-Alix; Scott, Edward R. D.

    2015-01-01

    origin. Although the Dawn mission did not detect mesosiderite-like material on Vesta, evidence linking the mesosiderites and HEDs includes: (i) theirnearly identical oxygen isotope compositions; (ii) the presence in both of coarse-grained Mg-rich olivines; (iii) both have synchronous Lu-Hf and Mn-Cr ages...

  17. Characterization of the sedimentary organic matter preserved in Messel oil shale by bulk geochemistry and stable isotopes

    NARCIS (Netherlands)

    Bauersachs, T.; Schouten, S.; Schwark, L.

    2014-01-01

    We investigated a 150 m thick drill core section of Messel oil shale using bulk geochemical and stable isotope techniques in order to determine the organic matter sources and the environmental conditions that prevailed during the deposition of the lacustrine sequence. High Corg values (on average

  18. Combined iron and magnesium isotope geochemistry of pyroxenite xenoliths from Hannuoba, North China Craton: implications for mantle metasomatism

    Science.gov (United States)

    Zhao, Xin Miao; Cao, Hui Hui; Mi, Xue; Evans, Noreen J.; Qi, Yu Han; Huang, Fang; Zhang, Hong Fu

    2017-06-01

    We present high-precision iron and magnesium isotopic data for diverse mantle pyroxenite xenoliths collected from Hannuoba, North China Craton and provide the first combined iron and magnesium isotopic study of such rocks. Compositionally, these xenoliths range from Cr-diopside pyroxenites and Al-augite pyroxenites to garnet-bearing pyroxenites and are taken as physical evidence for different episodes of melt injection. Our results show that both Cr-diopside pyroxenites and Al-augite pyroxenites of cumulate origin display narrow ranges in iron and magnesium isotopic compositions (δ57Fe = -0.01 to 0.09 with an average of 0.03 ± 0.08 (2SD, n = 6); δ26Mg = - 0.28 to -0.25 with an average of -0.26 ± 0.03 (2SD, n = 3), respectively). These values are identical to those in the normal upper mantle and show equilibrium inter-mineral iron and magnesium isotope fractionation between coexisting mantle minerals. In contrast, the garnet-bearing pyroxenites, which are products of reactions between peridotites and silicate melts from an ancient subducted oceanic slab, exhibit larger iron isotopic variations, with δ57Fe ranging from 0.12 to 0.30. The δ57Fe values of minerals in these garnet-bearing pyroxenites also vary widely (-0.25 to 0.08 in olivines, -0.04 to 0.25 in orthopyroxenes, -0.07 to 0.31 in clinopyroxenes, 0.07 to 0.48 in spinels and 0.31-0.42 in garnets). In addition, the garnet-bearing pyroxenite shows light δ26Mg (-0.43) relative to the mantle. The δ26Mg of minerals in the garnet-bearing pyroxenite range from -0.35 for olivine and orthopyroxene, to -0.34 for clinopyroxene, 0.04 for spinel and -0.68 for garnet. These measured values stand in marked contrast to calculated equilibrium iron and magnesium isotope fractionation between coexisting mantle minerals at mantle temperatures derived from theory, indicating disequilibrium isotope fractionation. Notably, one phlogopite clinopyroxenite with an apparent later metasomatic overprint has the heaviest δ57Fe

  19. Isotope geochemistry of fluid inclusions in Permian halite with implications for the isotopic history of ocean water and the origin of saline formation waters

    International Nuclear Information System (INIS)

    Knauth, L.P.; Beeunas, M.A.

    1986-01-01

    deltaD and delta 18 O values have been determined for fluid inclusions in 45 samples of Permian halite. The inclusions are enriched in 18 O relative to the meteoric water line but are depleted in D relative to ocean water. Inclusions with the more positive delta-values coincide with the isotopic compositions expected for evaporating sea water which follows a hooked trajectory on a deltaD-delta 18 O diagram. Inclusions with more negative delta-values may represent more highly evaporated sea water but probably reflect synsedimentary or diagenetic mixing to those of a modern evaporite pan to indicate that Permian sea water was isotopically similar to modern sea water. Connate evaporite brines can have negative delta-values because of the probable hooked isotope trajectory of evaporating sea water and/or synsedimentary mixing of evaporite brines with meteoric waters. (author)

  20. Production of strontium-82 for the Cardiogen trademark PET generator: a project of the Department of Energy Virtual Isotope Center

    International Nuclear Information System (INIS)

    Phillips, D.R.; Peterson, E.J.; Taylor, W.A.; Jamriska, D.J.; Hamilton, V.T.; Kitten, J.J.; Valdez, F.O.; Salazar, L.L.; Pitt, L.R.; Heaton, R.C.; Kolsky, K.L.; Mausner, L.F.; Kurczak, S.; Zhuikov, B.L.; Kokhanyuk, V.M.; Konyakhin, N.A.; Nortier, F.M.; Walt, T.N. van der; Hanekom, J.; Sosnowski, K.M.; Carty, J.S.

    2000-01-01

    In December of 1989, the United States Food and Drug Administration approved 82 Rb chloride in saline solution for cardiological perfusion imaging by positron emission tomography (PET). The solution is derived from a 82 Sr generator system that is presently manufactured by Bristol Myers Squibb and distributed for clinical application in the United States by Bracco Diagnostics, Inc. Many years of research and development by people in several institutions led up to the approval for clinical use. Currently, there are about 15 sites in the U.S. that perform clinical myocardial perfusion imaging by PET using 82 Rb chloride from the generator. In order to manufacture the generators, Bristol Myers Squibb requires about 1600 mCi of 82 Sr every 30 days. The United States Department of Energy and MDS Nordion, Canada are the current suppliers with qualified Drug Master Files for the production and distribution of this nuclide for the Cardiogen trademark generator. These two entities have worked together over the years to assure the regular, reliable supply of the 82 Sr. Here we describe the facilities and methods used by the Department of Energy in its Virtual Isotope Center to make and distribute the nuclide. (orig.)

  1. Geochemistry, water balance, and stable isotopes of a “clean” pit lake at an abandoned tungsten mine, Montana, USA

    International Nuclear Information System (INIS)

    Gammons, Christopher H.; Pape, Barbara L.; Parker, Stephen R.; Poulson, Simon R.; Blank, Carrine E.

    2013-01-01

    Highlights: • An abandoned open pit mine is now a 30 m deep lake with excellent water quality. • Concentrations of sulfate, nutrients, and most trace metals are extremely low. • Based on water isotopes, the lake is 30% evaporated with a 2.5 yr residence time. • Stable isotopes of DIC and DO track in-lake bio-geochemical processes. • Phytoplankton are active at depths as great as 20 m. - Abstract: The Calvert Mine is a small tungsten-rich (scheelite) skarn deposit in a remote, mountainous region of southwest Montana, USA. The open-pit mine closed in the 1970s and subsequently flooded to form a pit lake that is roughly conical in shape, 30 m deep and 120 m in diameter, with no surface inlet or outlet. The lake is holomictic with a groundwater flow-through hydrology and an estimated residence time of 2.5–5 y. Water isotopes show that the lake is at an approximate steady state with respect to water balance and has experienced 30% evaporation. The lake has a near-neutral pH, exceptional clarity, and extremely low concentrations of nutrients, sulfate, and most metals, including tungsten. Manganese concentrations are slightly elevated and increase with depth towards the sediment–water interface. Despite seasonally anoxic conditions in the deep water, dissolved Fe concentrations are orders of magnitude lower than Mn, suggesting that insufficient organic carbon is present in the sediment of this oligotrophic lake to drive bacterial Fe reduction. Based on stable isotope fingerprinting, diffuse seepage that enters a nearby headwater stream at the base of a large waste-rock pile can be directly linked to the partially evaporated pit lake. However, this seepage has neutral pH and low metal concentrations, and poses no threats to the environment. Stable isotopes of dissolved inorganic carbon (DIC) and dissolved oxygen (DO) are used to track the relative importance of photosynthesis and respiration with depth. In summer, a zone of high productivity exists near the

  2. Using Stable Isotope Geochemistry to Determine Changing Paleohydrology and Diagenetic Alteration in the Late Cretaceous Kaiparowits Formation, UT USA

    Science.gov (United States)

    Yamamura, Daigo

    The Western Interior Basin of the North America preserves one of the best sedimentary and paleontological records of the Cretaceous in the world. The Upper Cretaceous Kaiparowits Formation is a rapidly deposited fluvial sequence and preserves one of the most complete terrestrial fossil record of the North America. Such a unique deposit provides an opportunity to investigate the interaction between the physical environment and ecology. In an effort to decipher such interaction, stable isotope composition of cements in sedimentary rocks, concretions and vertebrate fossils were analyzed. Despite the difference in facies and sedimentary architecture, the isotope composition does not change significantly at 110 m from the base of the formation. Among the well-preserved cement samples, stable isotope composition indicates a significant hydrologic change within the informal Middle unit; a 6.37‰ depletion in delta13C and 3.30‰ enrichment in delta 18O occurs at 300 m above the base of the formation. The isotope values indicate that the sandstone cements below 300 m were precipitated in a mixing zone between marine and terrestrial groundwater, whereas the cements in upper units were precipitated in a terrestrial groundwater. Despite the difference in physical appearance (i.e. color and shape), the isotopic compositions of cements in concretions are similar to well-cemented sandstone bodies in similar stratigraphic positions. Isotope compositions of the host rock are similar to that of mudrock and weathered sandstone, suggesting the origin of cementing fluids for the sandstone and concretions were the same indicating that: 1) the concretions were formed in shallow groundwater and not related to the groundwater migration, or 2) all cements in upper Kaiparowits Formation are precipitated or altered during later stage groundwater migration. Average delta18Oc from each taxon show the same trend as the delta18Op stratigraphic change, suggesting delta18Oc is still useful as a

  3. The Leadville Mine Drainage Tunnel Catastrophe: A Case Study of How Isotope Geochemistry Provided Forensic Evidence to Inform Policy Decisions

    Science.gov (United States)

    Williams, M. W.; Wireman, M.; Liu, F.; Gertson, J.

    2008-12-01

    A state of emergency was declared in February 2008 because of fears that a blocked drainage tunnel in the Leadville mining district of Colorado could cause a catastrophic flood. An estimated 1 billion gallons of metals-laden water poses an eminent threat to the city of Leadville and the headwaters of the Arkansas river. Within days of the declaration of a state of emergency, Governor Ritter and Senator Salazer of Colorado, along with a host of other local and statewide politicians, visited the site and emphasized the need to develop a fast yet safe mitigation plan. Here we provide information from a case study that illustrates how a suite of isotopic and hydrologic tools enables identification of critical, site-specific variables essential in developing a science plan to guide targeted remediation of the Leadville drainage tunnel. The isotopic tools, including both stable and radiogenic isotopes, provided clear and compelling evidence of water sources and flowpaths in an area that has undergone extensive perturbations, including the drilling of more than 2,000 mine shafts. This forensic evidence was the key information in developing a plan to plug the drainage tunnel several hundred feet underground, divert a major source of polluted water from reaching the collapsed tunnel and piping it to an existing treatment plant, and guidance on where to place pumps in additional mine shafts, and the drilling of new wells to pump water in case the plugging of the tunnel caused water to pool up and raise the water table to dangerous heights. This particular case of forensic hydrology using isotopic tools not only provides the scientific basis for an operational plan to defuse a life- and property-threatening situation, it also provides the basis for decommissioning an existing water treatment plant, which will result in savings of over 1 million annually in operational costs. Decommissioning the existing water treatment plant will pay for the tunnel mitigation within several

  4. New Rb-Sr isotopic ages and geochemistry of granitic gneisses from southern Bastar: implications for crustal evolution

    International Nuclear Information System (INIS)

    Sarkar, G.; Gupta, S.N.; Bishui, P.K.

    1994-01-01

    Deformed gneisses from the southern Bastar craton yield Rb-Sr whole-rock ages of 2560 Ma and 2659 Ma with initial Sr ratios ranging between 0.70899 and 0.70726 respectively. The isotopic data are found to be scattered even at the outcrop scale which possibly indicate large-scale reworking of the gneisses during the period. The high initial Sr ratios that associate with scattering of the isotopic data reflect reworking of older gneisses. Geochemically, these gneisses are considered to be derived from an amphibolitic or basaltic protolith. The 2095 Ma (initial Sr ratio of 0.74312) old leucocratic granite intrusive into these gneisses represent early Proterozoic magmatic activity. Based on the available isotopic and geochemical data, it is suggested that the Bastar craton represents a polyphase, multicomponent terrain developed by repeated magmatism at a much earlier, probably during mid-Archaean, time and was extensively reworked during the time span between end-Archaean and early Proterozoic period. This reworking may be synchronous with coalescing of smaller crustal components possibly during the end-Archaean time. (author). 21 refs., 5 figs., 2 tabs

  5. Mineralogy, Geochemistry and Stable Isotope Investigation of Gürkuyu Sb Mineralization (Gediz-Kütahya-NW Turkey

    Directory of Open Access Journals (Sweden)

    Yeşim ÖZEN

    2016-11-01

    Full Text Available Abstract. The Gürkuyu Sb mineralization is located in the western part of Anatolian tectonic belt, in southern part of İzmir-Ankara zone and in northern part of Menderes Massif. The mineralization located at west of the Koca hill in east of Gürkuyu village of Gediz (Kütahya-Turkey has been characterized through the detailed examinations involving sulfur and oxygen isotope. Serpentinites of Dağardı melange and crystallized limestones of Budağan limestone were hydrothermally altered by hydrothermal solutions, come from fissures and fractures due to tectonic movement during the thrust of melange and occurred silicified zone. Gürkuyu Sb mineralization suggest that occurred in this silicified zone. In Gürkuyu mineralization, primary ore minerals are antimonite and pyrite, secondary ore minerals are senarmontite, valentinite, orpiment and realgar. Quartz and calcite are the most common gangue minerals. In Gürkuyu Sb mineralization, δ34S values of stibnite are ranged from 1.0 ‰ to 1.3 ‰. δ18O values of quartz are ranged is 15.8 ‰ in Gürkuyu mineralization. Sulfur and oxygen isotope values are similar to the values for magmatic rocks and to the values for fluids of magmatic origin.Keywords: Stable isotope, Gürkuyu, Sb mineralization, Gediz, Kütahya, NW Turkey.

  6. Elemental hydrochemistry and hydro geochemistry of the uranium isotopes in Alter do Chao formation, Manaus (Amazon - Brazil)

    International Nuclear Information System (INIS)

    Silva, Marcio Luiz da; Bonotto, Daniel Marcos

    2006-01-01

    The water exploitation at Manaus city, Amazonas State, Brazil, takes place from Negro River and tubular wells, being performed by a private company. This paper evaluates the hydrochemistry and geochemical behavior of uranium isotopes ( 238 U and 234 U) in groundwaters from Manaus city, with the aim to characterize the contaminants or pollutants that possibly are affecting the quality of the underground hydrological resources, as well as to evaluate the potential use of the natural U-isotopes as hydrological tracers in the aquifer studied. The U-isotopes analysis allowed to determine 234 U/ 238 U activity ratios of 1.2-4.4, and dissolved uranium concentration of 0.003-1.1 μg.L -1 (ppb). These results and those concerning the others parameters indicated that the waters are appropriate for human consumption, permitting to classify the hydrological system as acid-reducing, and to say that the waters leach minerals in strata containing low U content.(author)

  7. Assessment of the origin and geothermal potential of the thermal waters by hydro-isotope geochemistry: Eskisehir province, Turkey.

    Science.gov (United States)

    Yuce, Galip; Italiano, Francesco; Yasin, Didem; Taskiran, Lutfi; Gulbay, Ahmet Hilmi

    2017-05-01

    The thermal fluids vented over Eskisehir province have been investigated for their origin and to estimate the geothermal potential of the area. Thermal waters as well as bubbling and dissolved gases were collected and analysed for their chemical and isotopic features. Their isotopic composition varies in the range from -11.5 to -7.7 ‰ for δ 18 O, -84 and -57 ‰ for δ 2 H, and 0-7.2 TU for tritium. The gases (bubbling and dissolved) are mostly N 2 -dominated with a significant amount of CO 2 . The helium isotopic ratios are in the range of 0.2-0.66 R/Rac, indicate remarkable mantle-He contribution ranging between 2 and 10 % in the whole study area. Considering the estimated geothermal gradient about three times higher than the normal gradient, and the reservoir temperatures estimated to be between 50 and 100 °C using quartz and chalcedony geothermometers, a circulation model was built where possible mixing with shallow waters cool down the uprising geothermal fluids.

  8. Zircon U-Pb chronology, geochemistry and Sr-Nd-Pb isotopic compositions of the Volcanic Rocks in the Elashan area, NW China: petrogenesis and tectonic implications

    Science.gov (United States)

    Zhou, H.; Wei, J.; Shi, W.; Li, P.; Chen, M.; Zhao, X.

    2017-12-01

    Elashan area is located in the intersection of the East Kunlun Orogenic Belt (EKOB) and the West Qinling Orogenic (WQOB). We present petrology, zircon U-Pb ages, whole-rock geochemistry and Sr-Nd-Pb isotopic compositions from the andesite and felsic volcanic rocks (rhyolite and rhyolitic tuffs) in Elashan group volcanic rock. The LA-ICP-MS zircon U-Pb age data indicate that the volcanic rocks are emplaced at 250 247 Ma. The volcanic rocks have high -K and aluminum - peraluminous characteristics, A/CNK = 1.07 1.82, δ ranges from 1.56 2.95, the main body is calc-alkaline rock. They are enriched in large ion lithophile elements (LILEs) and light rare earth elements (LREEs) and depleted in some high field strength elements (HFSEs, e.g., Nb, Ta, P and Ti), while having a flat heavy REE (HREEs) pattern. The ∑REE values of 178.68 to 298.11 ppm, average 230.50 ppm. The LREE/HREE values of 4.39 to 11.78 ppm, average 6.77 ppm. REE fractionation is obvious, REE distribution curve was right smooth, and have slightly negative Eu anomalies (Eu/Eu*=0.44-0.80, average 0.60), which as similar to the island arc volcanic rocks. The volcanic rocks have initial 87Sr/86Sr ratios of 0.71028-0.71232, ɛNd(t) values of -6.7 to -7.6, with T2DM-Nd ranging from 1561 to 1640 Ma. Pb isotopic composition (206 Pb / 204 Pb)t = 18.055 18.330, (207 Pb / 204 Pb)t = 15.586 15.618, (208 Pb / 204 Pb)t = 37.677 38.332. Geochemical and Sr-Nd-Pb isotopes indicates that Elashan group volcanic magma derived mainly from the lower crust. Elashan group volcanic rocks is the productive East Kunlun block and West Qinling block collision, which makes the thicken crust caused partial melting in the study area. The source rocks is probably from metamorphic sandstone of Bayankala. But with Y-Nb and Rb-(Y+Nb), R1-R2 and Rb/10-Hf-Ta*3 diagrams showing that intermediate-acid rocks mainly formed in volcanic arc-collision environment, probably the collision event is short , therefore rocks retain the original island

  9. Hydrochemistry, mineralogy and sulfur isotope geochemistry of acid mine drainage at the Mt. Morgan mine environment, Queensland, Australia

    International Nuclear Information System (INIS)

    Edraki, M.; Golding, S.D.; Baublys, K.A.; Lawrence, M.G.

    2005-01-01

    Mineralogical, hydrochemical and S isotope data were used to constrain hydrogeochemical processes that produce acid mine drainage from sulfidic waste at the historic Mount Morgan Au-Cu mine, and the factors controlling the concentration of SO 4 and environmentally hazardous metals in the nearby Dee River in Queensland, Australia. Some highly contaminated acid waters, with metal contents up to hundreds of orders of magnitude greater than the Australia-New Zealand environmental standards, by-pass the water management system at the site and drain into the adjacent Dee River. Mine drainage precipitates at Mt. Morgan were classified into 4 major groups and were identified as hydrous sulfates and hydroxides of Fe and Al with various contents of other metals. These minerals contain adsorbed or mineralogically bound metals that are released into the water system after rainfall events. Sulfate in open pit water and collection sumps generally has a narrow range of S isotope compositions (δ 34 S = 1.8-3.7%o) that is comparable to the orebody sulfides and makes S isotopes useful for tracing SO 4 back to its source. The higher δ 34 S values for No. 2 Mill Diesel sump may be attributed to a difference in the source. Dissolved SO 4 in the river above the mine influence and 20 km downstream show distinctive heavier isotope compositions (δ 34 S = 5.4-6.8%o). The Dee River downstream of the mine is enriched in 34 S (δ 34 S = 2.8-5.4%o) compared with mine drainage possibly as a result of bacterial SO 4 reduction in the weir pools, and in the water bodies within the river channel. The SO 4 and metals attenuate downstream by a combination of dilution with the receiving waters, SO 4 reduction, and the precipitation of Fe and Al sulfates and hydroxides. It is suggested here that in subtropical Queensland, with distinct wet and dry seasons, temporary reducing environments in the river play an important role in S isotope systematics

  10. 'Applications of stable isotopes in life sciences'. Lead and strontium stable isotope measurements by using a high lateral resolution secondary ion mass spectrometer (NanoSIMS)

    International Nuclear Information System (INIS)

    Sano, Yuji

    2008-01-01

    The method of Pb and Sr isotope measurements at about 5 μm resolution was developed by using a high lateral resolution secondary ion mass spectrometer (NanoSIMS NS50). Since the both elements have radiogenic nuclides such as 206 Pb, 207 Pb, and 87 Sr, natural variations of isotopic ratios are large. It is possible to detect a meaningful variation in a terrestrial sample, even though the experimental error is relatively large. In the case of monazite U-Pb dating, a 4 nA O - primary beam was used to sputter the sample and secondary positive ions were extracted for mass analysis using a Mattauch-Herzog geometry. The multi-collector system was modified to detect 140 Ce + , 204 Pb + , 206 Pb + , 238 U 16 O + , and 238 U 16 O 2 + ions simultaneously. Based on the monazite standard from North-Central Madagascar, we have determined the 206 Pb/ 238 U ratios of samples. 207 Pb/ 206 Pb ratios were measured by a magnet scanning with a single collector mode. 44 monazite grains extracted from a sedimentary rock in Taiwan were analyzed. Observed ages were consistent with the U-Th-Pb chemical ages by EPMA. Then NanoSIMS has been used to measure 87 Sr/ 86 Sr ratios in natural calcium carbonate samples. Multi-collector system was adjusted to detect 43 Ca + , 80 Ca 2 + , 86 Sr + , and 87 Sr + ions at the same time. Magnetic field was scanning for the EM no.4 counter to detect 85 Rb + , 86 Sr + and 87 Sr + , while the EM no.4b can measure 86 Sr + , 87 Sr + , and 88 Sr + , respectively. Repeated analyses of a coral skeleton standard (JCp-1) show that 87 Sr/ 86 Sr ratio agrees well with the seawater signature, after the series of corrections such as Ca dimer, 87 Rb, and a mass bias estimated by 88 Sr/ 86 Sr ratio. The method is applied to an otolith from ayu (Pleco-glossus altivelis altivelis) collected from the Yodo river, Japan. The spatial variation of 87 Sr/ 86 Sr ratios was consistent with amphidromous migration of the fish, namely, born in the lake and grown in the coastal sea

  11. Amino acid stable isotope applications to deep-sea corals: A molecular geochemistry approach to reconstructing past ocean conditions

    Science.gov (United States)

    McMahon, K.; McCarthy, M. D.; Guilderson, T. P.; Sherwood, O.; Williams, B.; Larsen, T.; Glynn, D. S.

    2017-12-01

    Future climate change is predicted to alter ocean productivity, food web dynamics, biogeochemical cycling, and the efficacy of the biological pump. Proteinaceous deep-sea corals act as "living sediment traps," providing long-term, high-resolution records of exported surface ocean production and a window into past changes in ocean condition as a historical context for potential future changes. Here, we present recent work developing the application of compound-specific stable isotope analysis of individual amino acids to proteinaceous deep-sea corals to reconstruct past changes in phytoplankton community composition and biogeochemical cycling. We present new calibrations for molecular isotope comparisons between metabolically active coral polyp tissue and bioarchival proteinaceous skeleton. We then applied these techniques to deep-sea corals from the North Pacific Subtropical Gyre (NPSG) to reconstruct centennial to millennial time scale changes in phytoplankton community composition and biogeochemical cycling as a function of regional climate change. This work suggests that the NPSG has undergone multiple major phytoplankton regime shifts over the last millennium between prokaryotic and eukaryotic phytoplankton communities and associated sources of nitrogen fueling production. The most recent regime, which started around the end of the Little Ice Age and the onset of the Industrial era, is unprecedented in the last 1000 years and resulted in a 30-50% increase in diazotrophic cyanobacteria contribution to export production and an associated 17-27% increase in N2-fixation in the NPSG over last century. By offering the first direct phylogenetic context for long-term shifts in isotopic records of exported particulate organic matter, our data represent a major step forward in understanding the evolution of marine plankton community dynamics, food web architecture, biogeochemical cycling, and the climate feedback loops through the biological pump.

  12. Strontium Isotopic Composition of Paleozoic Carbonate Rocks in the Nevada Test Site Vicinity, Clark, Lincoln, and Nye Counties, Nevada and Inyo County, California

    International Nuclear Information System (INIS)

    James B. Paces; Zell E. Peterman; Kiyoto Futa; Thomas A. Oliver; Brian D. Marshall.

    2007-01-01

    Ground water moving through permeable Paleozoic carbonate rocks represents the most likely pathway for migration of radioactive contaminants from nuclear weapons testing at the Nevada Test Site, Nye County, Nevada. The strontium isotopic composition (87Sr/86Sr) of ground water offers a useful means of testing hydrochemical models of regional flow involving advection and reaction. However, reaction models require knowledge of 87Sr/86Sr data for carbonate rock in the Nevada Test Site vicinity, which is scarce. To fill this data gap, samples of core or cuttings were selected from 22 boreholes at depth intervals from which water samples had been obtained previously around the Nevada Test Site at Yucca Flat, Frenchman Flat, Rainier Mesa, and Mercury Valley. Dilute acid leachates of these samples were analyzed for a suite of major- and trace-element concentrations (MgO, CaO, SiO2, Al2O3, MnO, Rb, Sr, Th, and U) as well as for 87Sr/86Sr. Also presented are unpublished analyses of 114 Paleozoic carbonate samples from outcrops, road cuts, or underground sites in the Funeral Mountains, Bare Mountain, Striped Hills, Specter Range, Spring Mountains, and ranges east of the Nevada Test Site measured in the early 1990's. These data originally were collected to evaluate the potential for economic mineral deposition at the potential high-level radioactive waste repository site at Yucca Mountain and adjacent areas (Peterman and others, 1994). Samples were analyzed for a suite of trace elements (Rb, Sr, Zr, Ba, La, and Ce) in bulk-rock powders, and 87Sr/86Sr in partial digestions of carbonate rock using dilute acid or total digestions of silicate-rich rocks. Pre-Tertiary core samples from two boreholes in the central or western part of the Nevada Test Site also were analyzed. Data are presented in tables and summarized in graphs; however, no attempt is made to interpret results with respect to ground-water flow paths in this report. Present-day 87Sr/86Sr values are compared to values

  13. The Serchio River catchment, northern Tuscany: Geochemistry of stream waters and sediments, and isotopic composition of dissolved sulfate

    International Nuclear Information System (INIS)

    Cortecci, Gianni; Dinelli, Enrico; Boschetti, Tiziano; Arbizzani, Paola; Pompilio, Loredana; Mussi, Mario

    2008-01-01

    The Serchio River and its tributaries in northern Tuscany were investigated for the chemical and isotopic compositions of waters and bed sediments. Bedrocks are mostly limestone/dolomite and siliciclastics, thermal spring systems are present in the catchment, and the main industrial activity is represented by paper-mills. Main results obtained are: (1) major ions in solution appear to be basically controlled by precipitation and lithology, as well as subordinately by direct inputs of thermal springs, (2) human influence on metals in the waters along the main Serchio and Lima rivers is indicated at a number of sites by increases in concentration compared to the chemical composition of upstream tributaries, (3) S and O isotope compositions delineate two main sources for aqueous SO 4 2- , that is dissolution of Triassic evaporite (directly or via thermal springs) and oxidation of sulfide dispersed in siliciclastic rocks. Anthropogenic contributions are probable, but they cannot be quantitatively assessed. Only SO 4 2- in the notoriously polluted Ozzeri tributary is suspected to be largely anthropogenic, and (4) the chemical composition of bed sediments is mainly influenced by lithology, apart from a number of technogenic elements in the upper part of the Serchio River and in some tributaries. Contamination possibly occurs at other sites, but geochemical indications are weak

  14. Alunite in the Pascua-Lama high-sulfidation deposit: Constraints on alteration and ore deposition using stable isotope geochemistry

    Science.gov (United States)

    Deyell, C.L.; Leonardson, R.; Rye, R.O.; Thompson, J.F.H.; Bissig, T.; Cooke, D.R.

    2005-01-01

    The Pascua-Lama high-sulfidation system, located in the El Indio-Pascua belt of Chile and Argentina, contains over 16 million ounces (Moz) Au and 585 Moz Ag. The deposit is hosted primarily in granite rocks of Triassic age with mineralization occurring in several discrete Miocene-age phreatomagmatic breccias and related fracture networks. The largest of these areas is Brecha Central, which is dominated by a mineralizing assemblage of alunite-pyrite-enargite and precious metals. Several stages of hydrothermal alteration related to mineralization are recognized, including all types of alunite-bearing advanced argillic assemblages (magmatic-hydrothermal, steam-heated, magmatic steam, and supergene). The occurrence of alunite throughout the paragenesis of this epithermal system is unusual and detailed radiometric, mineralogical, and stable isotope studies provide constraints on the timing and nature of alteration and mineralization of the alunite-pyiite-enargite assemblage in the deposit. Early (preore) alteration occurred prior to ca. 9 Ma and consists of intense silicic and advanced argillic assemblages with peripheral argillic and widespread propylitic zones. Alunite of this stage occurs as fine intergrowths of alunite-quartz ?? kaolinite, dickite, and pyrophyllite that selectively replaced feldspars in the host rock. Stable isotope systematics suggest a magmatic-hydrothermal origin with a dominantly magmatic fluid source. Alunite is coeval with the main stage of Au-Ag-Cu mineralization (alunite-pyrite-enargite assemblage ore), which has been dated at approximately 8.8 Ma. Ore-stage alunite has an isotopic signature similar to preore alunite, and ?? 34Salun-py data indicate depositional temperatures of 245?? to 305??C. The ??D and ?? 18O data exclude significant involvement of meteoric water during mineralization and indicate that the assemblage formed from H2S-dominated magmatic fluids. Thick steam-heated alteration zones are preserved at the highest elevations in

  15. Gas and Isotope Geochemistry of 81 Steam Samples from Wells in The Geysers Geothermal Field, Sonoma and Lake Counties, California

    Science.gov (United States)

    Lowenstern, Jacob B.; Janik, Cathy J.; Fahlquist, Lynne; Johnson, Linda S.

    1999-01-01

    The Geysers geothermal field in northern California, with about 2000-MW electrical capacity, is the largest geothermal field in the world. Despite its importance as a resource and as an example of a vapor-dominated reservoir, very few complete geochemical analyses of the steam have been published (Allen and Day, 1927; Truesdell and others, 1987). This report presents data from 90 steam, gas, and condensate samples from wells in The Geysers geothermal field in northern California. Samples were collected between 1978 and 1991. Well attributes include sampling date, well name, location, total depth, and the wellhead temperature and pressure at which the sample was collected. Geochemical characteristics include the steam/gas ratio, composition of noncondensable gas (relative proportions of CO2, H2S, He, H2, O2, Ar, N2, CH4, and NH3), and isotopic values for deltaD and delta18O of H2O, delta13C of CO2, and delta34S of H2S. The compilation includes 81 analyses from 74 different production wells, 9 isotopic analyses of steam condensate pumped into injection wells, and 5 complete geochemical analyses on gases from surface fumaroles and bubbling pools. Most samples were collected as saturated steam and plot along the liquid-water/steam boiling curve. Steam-togas ratios are highest in the southeastern part of the geothermal field and lowest in the northwest, consistent with other studies. Wells in the Northwest Geysers are also enriched in N2/Ar, CO2 and CH4, deltaD, and delta18O. Well discharges from the Southeast Geysers are high in steam/gas and have isotopic compositions and N2/Ar ratios consistent with recharge by local meteoric waters. Samples from the Central Geysers show characteristics found in both the Southeast and Northwest Geysers. Gas and steam characteristics of well discharges from the Northwest Geysers are consistent with input of components from a high-temperature reservoir containing carbonrich gases derived from the host Franciscan rocks. Throughout the

  16. Iodine budget in surface waters from Atacama: Natural and anthropogenic iodine sources revealed by halogen geochemistry and iodine-129 isotopes

    International Nuclear Information System (INIS)

    Álvarez, Fernanda; Reich, Martin; Snyder, Glen; Pérez-Fodich, Alida; Muramatsu, Yasuyuki; Daniele, Linda; Fehn, Udo

    2016-01-01

    Iodine enrichment in the Atacama Desert of northern Chile is widespread and varies significantly between reservoirs, including nitrate-rich “caliche” soils, supergene Cu deposits and marine sedimentary rocks. Recent studies have suggested that groundwater has played a key role in the remobilization, transport and deposition of iodine in Atacama over scales of millions-of-years. However, and considering that natural waters are also anomalously enriched in iodine in the region, the relative source contributions of iodine in the waters and its extent of mixing remain unconstrained. In this study we provide new halogen data and isotopic ratios of iodine ("1"2"9I/I) in shallow seawater, rivers, salt lakes, cold and thermal spring water, rainwater and groundwater that help to constrain the relative influence of meteoric, marine and crustal sources in the Atacama waters. Iodine concentrations in surface and ground waters range between 0.35 μM and 26 μM in the Tarapacá region and between 0.25 μM and 48 μM in the Antofagasta region, and show strong enrichment when compared with seawater concentrations (I = ∼0.4 μM). In contrast, no bromine enrichment is detected (1.3–45.7 μM for Tarapacá and 1.7–87.4 μM for Antofagasta) relative to seawater (Br = ∼600 μM). These data, coupled to the high I/Cl and low Br/Cl ratios are indicative of an organic-rich sedimentary source (related with an “initial” fluid) that interacted with meteoric water to produce a mixed fluid, and preclude an exclusively seawater origin for iodine in Atacama natural waters. Iodine isotopic ratios ("1"2"9I/I) are consistent with halogen chemistry and confirm that most of the iodine present in natural waters derives from a deep initial fluid source (i.e., groundwater which has interacted with Jurassic marine basement), with variable influence of at least one atmospheric or meteoric source. Samples with the lowest isotopic ratios ("1"2"9I/I from ∼215 to ∼1000 × 10"

  17. Petrogenesis of Mesozoic granites in the Xitian, South China: Evidence from whole-rock geochemistry and zircon isotopes

    Science.gov (United States)

    Liu, Q.; Sun, J.; He, M.; Hou, Q.; Niu, R.

    2017-12-01

    Mesozoic granitoids are widespread in southeastern China, which accompanied with lots of world-famous polymetallic deposits. The mineralization is believed to be related to the Mesozoic granitic magmatism. However, the petrogenesis of these granites and their relation to the mineralization are still debated. As a typical granitic pluton, Xitian granites from the eastern Hunan Province are formed during this period and associated with tungsten-tin deposit. Whole-rock geochemical, SIMS zircon geochronology and oxygen isotopes, as well as LA-ICPMS zircon Lu-Hf isotopic analyses, were carried out on a suite of rocks from Xitian granitic pluton to constrain their magmatic sources and petrogenesis. Xitian granitic pluton is mainly composed of biotite adamellite, biotite granite, fine-grained granite. SIMS and LA-ICPMS U-Pb dating of zircons indicate that there are two episodes of these rocks, i.e., Late Triassic granites (227-233Ma) and Late Jurassic granites (150-154Ma). The Xitian granites are silica-rich, potassic and weakly peraluminous. Petrographic and geochemical features show that they are highly fractionated I-type granites. The combined elemental and isotopic results indicated that the Late Triassic granite in Xitian area experienced a process of crystal fractionation of crustal-derived magmas coupled with strong assimilation of the surrounding rocks. The occurrence of Jurassic granitoids in Xitian area is attributed to ascending of mantle-derived magmas, which provide heat for partial melting of crustal materials. The Late Jurassic granite may be derived from juvenile crust or partial melting of ancient crustal rocks, whereas high degrees of crystal fractionation further enriched tungsten-tin in the evolved granitic rocks. This work was financially supported by the Research Cooperation between Institute and University of Chinese Academy of Sciences grant (Y552012Y00), Public Welfare Project of the Ministry of land and Resources of China (201211024

  18. Isotope geochemistry of brasiliano age, coarsely porphyritic, K-calc-alkalic granitoids and associated K-diorites, northeast Brazil

    International Nuclear Information System (INIS)

    Sial, A.N.; Mariano, G.; Ferreira, V.P.

    1989-01-01

    Several porphyritic, K-calc-alkalic were syntectonically intruded in NE Brazil during the Brasiliano orogeny. They show bi-(qz) diorite and coarsely porphyritic granodiorite to qz monzonite ('Itaporanga-type') in commingling zones on a scale of cm to m irrespective of whether plutons are at the margins of the NE-trending Cachoeirinha-Salgueiro Fold Belt (CSF) or intruded metasediments of the Serido Fold Belt (SFB). The bi(qz) diorites are found in magmatic or stromatic structures and narrow dikes wich intruded the felsic facies. SiO 2 in the porphyritic facies ranges from 61 to 72% with K 2 O usually > Na 2 O. K-diorities exhibit SiO 2 from 50 to 58%, MgO from 2 to 10% and K 2 O from 2 to 5%. Both facies are usually Ba and Sr-enriched, with similar, highly fractionated REE patterns, lacking free of Eu anomaly. Quartz 180 values are considered homogeneous on the scale of these intrusions in the CSF, (8 to 10 per milSMOW). Bi-(qz) diorites exhibit slightly higher 180 (9.5 to 10.5 per milSMOW). In the SFB both facies are lower than 180. The oxygen isotope data for the porphyritic facies are compatible with I-type source with some metasedimentary component of variable proportion. As bi(qz) diorites were formed pre- to post-porphyritic facies intrusion, their high LREE, K and 180 reflect their source rather than the interaction with the potassic felsic magma. Preliminarly sulfur isotope values suggest that porphyritic facies of granitoids in the SBF are lower in 34S than those in the CSF. Rb and Sr isotopes reflect source heterogeneity, complicated by mixing relations. Ages span from 510 to 630 Ma suggesting that the Itaporanga-type association was formed during uplift and cooling of the Pan-African I and onset of the Pan-African II orogenies, recognized in West Africa. (author) [pt

  19. Isotope geochemistry of recent magmatism in the Aegean arc: Sr, Nd, Hf, and O isotopic ratios in the lavas of Milos and Santorini-geodynamic implications

    Science.gov (United States)

    Briqueu, L.; Javoy, M.; Lancelot, J.R.; Tatsumoto, M.

    1986-01-01

    In this comparative study of variations in the isotopic compositions (Sr, Nd, O and Hf) of the calc-alkaline magmas of the largest two volcanoes, Milos and Santorini, of the Aegean arc (eastern Mediterranean) we demonstrate the complexity of the processes governing the evolution of the magmas on the scale both of the arc and of each volcano. On Santorini, the crustal contamination processes have been limited, effecting the magma gradually during its differentiation. The most differentiated lavas (rhyodacite and pumice) are also the most contaminated. On Milos, by contrast, these processes are very extensive. They are expressed in the 143Nd/144Nd vs. 87Sr/86Sr diagram as a continuous mixing curve between a mantle and a crustal end member pole defined by schists and metavolcanic rocks outcropping on these volcanoes. In contrast with Santorini, the least differentiated lavas on Milos are the most contaminated. These isotopic singularities can be correlated with the geodynamic evolution of the Aegean subduction zone, consisting of alternating tectonic phases of distension and compression. The genesis of rhyolitic magmas can be linked to the two phases of distension, and the contamination of the calc-alkaline mantle-derived magmas with the intermediate compressive phase. The isotopic characteristics of uncontaminated calc-alkaline primitive magmas of Milos and Santorini are directly comparable to those of magmas generated in subduction zones for which a contribution of subducted sediments to partial melts from the mantle is suggested, such as in the Aleutian, Sunda, and lesser Antilles island arcs. However, in spite of the importance of the sediment pile in the eastern Mediterranen oceanic crust (6-10 km), the contribution of the subducted terrigenous materials remains of limited amplitude. ?? 1986.

  20. French days on stable isotopes

    International Nuclear Information System (INIS)

    2000-01-01

    These first French days on stable isotopes took place in parallel with the 1. French days of environmental chemistry. Both conferences had common plenary sessions. The conference covers all aspects of the use of stable isotopes in the following domains: medicine, biology, environment, tracer techniques, agronomy, food industry, geology, petroleum geochemistry, cosmo-geochemistry, archaeology, bio-geochemistry, hydrology, climatology, nuclear and particle physics, astrophysics, isotope separations etc.. Abstracts available on CD-Rom only. (J.S.)

  1. Geochronology, geochemistry and Hf–Sr–Nd isotopes of the ore-bearing syenite from the Shapinggou porphyry Mo deposit, East Qinling-Dabie orogenic belt

    Directory of Open Access Journals (Sweden)

    Tao He

    2016-12-01

    Full Text Available The Shapinggou Mo deposit is located in the western Dabie mountains, the eastern part of the Qinling-Dabie molybdenum orogenic belt. Shapinggou Mo deposit is a concealed deposit with the ore body mainly hosted by explosive breccia of Gaijing and the granite porphyry as well as the syenite of Shapinggou. Geochemistry study show that the SiO2 contents of Shapinggou syenite range from 61.74 to 69.93%, and the A/CNK from 0.95 to 1.06, classified as metaluminous to weak peraluminous, belonging to alkalic to shoshonitic series. The Mo deposits in Qinling Mo belt formed in two main periods, i.e., the first period occurred in to the Early Cretaceous (145–130 Ma, the second period in the late Early Cretaceous (130–110 Ma. Most of the Mo deposits in Dabie region formed in the second period. The results of zircon U–Pb show that the age of the Shapinggou syenite is 111.3 ± 1.2 Ma, which belongs to the second period. Proterozoic-Archean inherited zircons suggest that it may include some more ancient crustal material like Kongling group. The ɛHf(t values of Shapinggou syenite range from −15.6 to −8.0, TDM2(Hf from 1.7 to 2.16 Ga, respectively. The ɛNd(t values of the Shapinggou syenite range from −12.29 to −11.76, TDM2(Nd from 1.85 to 1.89 Ga, the 87Sr/86Sr from 0.709 to 0.710, respectively. Results of zircon Hf isotope and whole rock Sr–Nd isotope of Shapinggou syenite indicate that the Mo ore-forming materials were mainly generated from old Yangtze craton, e.g., gneiss from Dabie orogeny, mixed with some juvenal mantle materials. The geodynamics of the Shapinggou Mo deposit corresponded to an extension period in Eastern China, which caused by large scale lithospheric thinning. The delamination caused asthenosphere upwelling and crust-mantle interaction, which provided the ore-forming material and heat.

  2. 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

  3. Compound-specific isotope analysis of light elements using gas chromatography/combustion/isotope ratio mass spectrometry (GC/C/IRMS) and its application to geochemistry

    International Nuclear Information System (INIS)

    Naraoka, Hiroshi; Yamada, Keita; Matsumoto, Kohei; Ishiwatari, Ryoshi

    1997-01-01

    Compound-specific isotope analysis has been developed recently using gas chromatography/combustion/mass spectrometry (GC/C/IRMS). This paper summarizes principles and progress of GC/C/IRMS, and reviews recent some important works using this new method. GC/C/IRMS is a novel tool for (1) biomarker analysis in sediments and living matter, (2) paleoenvironment analysis including reconstruction of ancient biogeochemical processes, (3) geochemical cycle study of organic compounds in a terrestrial-marine system, (4) evaluation of maturity and diagenesis of organic matter including petroleum formation, (5) ecological analysis, (6) evaluation of anthropologenic pollution in environment, (7) detection of extraterrestrial organic compounds and the formation mechanism study, (8) tracer studies in environment. (author)

  4. Composition, oxygen isotope geochemistry, and origin of smectite in the metalliferous sediments of the Bauer Deep, southeast Pacific

    Energy Technology Data Exchange (ETDEWEB)

    Cole, T G [Imperial Coll. of Science and Technology, London (UK). Geology Dept.

    1985-01-01

    The sediments of the Bauer Deep, an open ocean basin situated on the northwest Nazca Plate in the southeast Pacific, constitute a regional metalliferous deposit dominated by authigenic smectite. Two 2-metre long cores from the Bauer Deep were examined to investigate the nature and origin of the smectite. Infra-red and Mossbauer spectroscopy, and wet chemical analysis (LiBO/sub 2/ fusion) of isolated smectite, indicate the mineral is a Mg-rich, Al-rich nontronite. Oxygen isotopic compositions for isolated smectite are uniform and translate to a non-hydrothermal temperature of formation of about 3 deg C. SEM observations show an abundance of well-preserved biogenic opal in surface and near surface sediment but postburial dissolution and transformation of this phase to smectite is evident at depth. Smectite formation is the result of interaction between iron oxyhydroxide, ponded in the Bauer Deep following a hydrothermal origin at the adjacent East Pacific Rise, and biogenic opal. A reaction mechanism is proposed. Regional factors control smectite formation. In particular, formation is inhibited in areas of CaCO/sub 3/ accumulation (topographic elevations) but favoured in areas of oxyhydroxide and opal ponding (topographic depressions.)

  5. Composition, oxygen isotope geochemistry, and origin of smectite in the metalliferous sediments of the Bauer Deep, southeast Pacific

    International Nuclear Information System (INIS)

    Cole, T.G.

    1985-01-01

    The sediments of the Bauer Deep, an open ocean basin situated on the northwest Nazca Plate in the southeast Pacific, constitute a regional metalliferous deposit dominated by authigenic smectite. Two 2-metre long cores from the Bauer Deep were examined to investigate the nature and origin of the smectite. Infra-red and Mossbauer spectroscopy, and wet chemical analysis (LiBO 2 fusion) of isolated smectite, indicate the mineral is a Mg-rich, Al-rich nontronite. Oxygen isotopic compositions for isolated smectite are uniform and translate to a non-hydrothermal temperature of formation of about 3 deg C. SEM observations show an abundance of well-preserved biogenic opal in surface and near surface sediment but postburial dissolution and transformation of this phase to smectite is evident at depth. Smectite formation is the result of interaction between iron oxyhydroxide, ponded in the Bauer Deep following a hydrothermal origin at the adjacent East Pacific Rise, and biogenic opal. A reaction mechanism is proposed. Regional factors control smectite formation. In particular, formation is inhibited in areas of CaCO 3 accumulation (topographic elevations) but favoured in areas of oxyhydroxide and opal ponding (topographic depressions.) (author)

  6. Gamow-Teller decay and nuclear deformation: implementing of a new total absorption spectrometer, study of isotopes N {approx_equal} Z krypton and strontium; Decroissance Gamow-Teller et deformation nucleaire: mise en oeuvre d'un nouveau spectrometre a absorption totale, etude d'isotopes N {approx_equal} Z de krypton et strontium

    Energy Technology Data Exchange (ETDEWEB)

    Poirier, E

    2002-12-01

    Nuclei with A {approx} 70 along the N=Z line are known to be the scene of phenomena closely related to the nuclear deformation and are of particular interest since theoretical mean field calculations predict that a large part of the Gamow-Teller resonance might be located below the ground state of the mother nucleus and then be accessible through {beta}-decay studies. These results have shown the effect of the shape of the ground state on the intensity of the Gamow-Teller strength. Thus, the experimental determination, through {delta}-decay, of the Gamow-Teller strength distribution and the comparison to the theoretical predictions allow to pin down the quadrupolar deformation parameter of the ground state of the parent nucleus. In order to study the neutron deficient isotopes of krypton (A=72,73,74,75) and strontium (A=76,77,78) and to establish the {beta}-strength on the full energy range, a new total absorption spectrometer (TAgS) has been built in the frame of an international collaboration and installed at the (SOLDE/CERN mass separator. For the data analysis, the response function R of the spectrometer has been calculated by means of Monte-Carlo simulations, based on the GEANT4 code, and of a statistical description of the level scheme in the daughter nucleus. The {beta}-feeding distribution has been obtained from experimental spectra through a method based on Bayes theorem and then converted into Gamow-Teller strength. The results coming from the {sup 74}Kr decay analysis allow to describe the ground state of such a nucleus as the coexistence of an oblate shape and of a prolate shape. In the case of {sup 76}Sr, the experimental Gamow-Teller strength distribution strongly indicates a prolate deformation. (author)

  7. Oxygen isotope geochemistry of the lassen volcanic center, California: Resolving crustal and mantle contributions to continental Arc magmatism

    Science.gov (United States)

    Feeley, T.C.; Clynne, M.A.; Winer, G.S.; Grice, W.C.

    2008-01-01

    This study reports oxygen isotope ratios determined by laser fluorination of mineral separates (mainly plagioclase) from basaltic andesitic to rhyolitic composition volcanic rocks erupted from the Lassen Volcanic Center (LVC), northern California. Plagioclase separates from nearly all rocks have ??18O values (6.1-8.4%) higher than expected for production of the magmas by partial melting of little evolved basaltic lavas erupted in the arc front and back-arc regions of the southernmost Cascades during the late Cenozoic. Most LVC magmas must therefore contain high 18O crustal material. In this regard, the ??18O values of the volcanic rocks show strong spatial patterns, particularly for young rhyodacitic rocks that best represent unmodified partial melts of the continental crust. Rhyodacitic magmas erupted from vents located within 3.5 km of the inferred center of the LVC have consistently lower ??18 O values (average 6.3% ?? 0.1%) at given SiO2 contents relative to rocks erupted from distal vents (>7.0 km; average 7.1% ?? 0.1%). Further, magmas erupted from vents situated at transitional distances have intermediate values and span a larger range (average 6.8% ?? 0.2%). Basaltic andesitic to andesitic composition rocks show similar spatial variations, although as a group the ??18O values of these rocks are more variable and extend to higher values than the rhyodacitic rocks. These features are interpreted to reflect assimilation of heterogeneous lower continental crust by mafic magmas, followed by mixing or mingling with silicic magmas formed by partial melting of initially high 18O continental crust (??? 9.0%) increasingly hybridized by lower ??18O (???6.0%) mantle-derived basaltic magmas toward the center of the system. Mixing calculations using estimated endmember source ??18O values imply that LVC magmas contain on a molar oxygen basis approximately 42 to 4% isotopically heavy continental crust, with proportions declining in a broadly regular fashion toward the

  8. Mineralization, geochemistry, fluid inclusion and sulfur stable isotope studies in the carbonate hosted Baqoroq Cu-Zn-As deposit (NE Anarak

    Directory of Open Access Journals (Sweden)

    Mohammad Ali Jazi

    2015-10-01

    bacterial sulfate reduction or by nonbacterial sulfate reduction through a reaction with organic materialin the sedimentary rocks (thermochemical sulfate reduction. However, the narrow range of δ34S and positive values indicates that they were not produced by bacterial sulfate reduction.Partial thermochemical reduction of sulfates has apparently produced light sulfurvalues (~ 21‰ lighter and it has been effective inthe deposition of ore minerals. Organic matter occurs as graphite in the Baqoroq formation in proximity of Baqoroq deposit (Cherepovsky et al., 1982. Discussion Epigenetic, stratabound and discordant Cu-Zn-As mineralization in the Baqoroq deposit occurs as open space filling of upper Cretaceous rocks. Host rock is partially dolomitized by ascending warm, saline fluids. Seawater sulfates were the source of the sulfidesulfur and the sulfate in the barite. The reduced sulfur was generated by partial thermochemical reduction and it was effective inthe deposition ofthe ore minerals. Based onthe evidence of carbonate host rocks, the absence of igneous activity, the open space filling texture, mineralogy, dolomite alteration, ore geochemistry (As and Sb high content and absence of Bi, microthermometric data of ore bearing fluid and sulfur isotope values, the Baqoroq deposit is very similar to the carbonate hosted copper deposits in Africa and in particular the Tsumeb deposit in Namibia. The Baqoroqdepositmay have been produced bymetamorphicfluids during orogenyrelated to theclosureof the Neo-Tethys ocean. References Cherepovsky, N., Plyaskin, V., Zhitinev, N., Kokorin, Y., Susov, M., Melnikov, B. and Aistov, L., 1982. Report on detailed geological prospecting in Anarak area (Central Iran Nakhlak locality. Geological Survey of Iran and Technoexport Company, Tehran. Report 14, 196 pp. Jazi, M.A., Karimpour, M.H., Malekzadeh, A. and Rahimi, B., 2015. Stratigraphic, lithological and structural controls in placement of Nakhlak deposit (northeast of Esfahan. Advanced

  9. Sr and Nd isotope geochemistry and tectonics during subduction and rifting in Sierra Santa Ursula, Sonora, Northwestern Mexico

    International Nuclear Information System (INIS)

    Mora-Klepeis, G.

    2000-01-01

    The western margin of North America was affected by a convergent plate boundary from the Cretaceous through the Early Tertiary. Volcanic rocks produced by subduction-related arc magmatism in northwestern Mexico are concentrated in two northwest-trending belts subparallel to the continental margin. One of these is the Sierra Madre Occidental, where mid-Tertiary magmatism consisted mostly of calc-alkaline rhyolitic ignimbrite and minor andesite produced between ∼ 46 and 28 Ma (McDowell et al., 1990). The second (younger) northwest-trending belt is located along the eastern margin of the Baja California Peninsula and in the Gulf of California region of mainland Mexico. This belt is composed mostly of andesite, but includes some basalt and dacite whose ages range from about 24 to 11 Ma (Hausback, 1984). A transition to rifting began after a mid-Tertiary cessation of subduction, eventually creating the Gulf of California extensional province. Four markedly different magma types comprising mainly tholeiitic and alkalic rocks and minor calc-alkaline and peralkaline rocks were erupted throughout the last 13 Ma and record the history of rifting of the Gulf of California (Sawlan, 1991). The aim of the present paper is to distinguish the nature of the 24-8.5 Ma magmatism emplaced on the eastern side of the Gulf of California in the state of Sonora, by the use of stratigraphic, geochemical and isotopic data. Preliminary Sr and Nd results show that three groups of magmas are present in the area suggesting a heterogeneous source. This can be interpreted as the result of magmas being erupted at different stages of subduction and rifting during the tectonic evolution of this part on North America

  10. Alteration mineralogy, mineral chemistry and stable isotope geochemistry of the Eocene pillow lavas from the Trabzon area, NE Turkey

    Science.gov (United States)

    Abdioğlu Yazar, Emel

    2018-02-01

    The Eocene subaqueous volcanic units in NE Turkey developed as pillow, closely packed pillow, isolated pillow, pillow breccia, hyaloclastite breccia and rare peperitic facies with red micritic limestones. They are locally set on volcaniclastic sandstone and claystone alternations and gradually pass to tuffs and volcanic breccias. The pillow lava samples generally exhibit intersertal, intergranular, microlitic porphyritic, variolitic, vesicular and glomeroporphyritic and glassy textures with clinopyroxene (Wo47-52En40-45Fs6-8), plagioclase (An10 to An96), olivine (Fo79-87) and Fe-Ti oxides (Usp0-0.27). Saponite, interlayered chlorite/saponite, rare beidellite and calcite were determined after olivine, rarely after plagioclase as well as in the glassy groundmass. Illite was restricted to plagioclase and the glassy groundmass. Na-Ca zeolites, chlorites/saponites, beidellite, dolomite and calcite occur as void infillings and in the glassy groundmass. Mineralogical, lithochemical and isotopic interpretations as well as thermometric calculations reveal a low-temperature seawater alteration in a semi-closed environment for the alteration of primary minerals and volcanic glass in addition to sealed vesicles and open systems for crosscutting veins. Due to the short exposure time intervals of seawater to rocks, the total chemistry of the rocks is not fully changed and most of the elements seem to be immobile, remaining in the system as a result of precipitation in voids and cracks. Thermometric estimations indicate that, the temperature of heated seawater is approximately 160 °C at the highest point especially in the vesicles, and decreases to approximately 85 °C due to circulation, resulting in alterations of the primary phases and volcanic glass.

  11. Study of the geochemistry of the cosmogenic isotope 10Be and the stable isotope 9Be in oceanic environment. Application to marine sediment dating

    International Nuclear Information System (INIS)

    Bourles, D.

    1988-01-01

    The radioisotope 10 Be is formed by spallation reactions in the atmosphere. It is transferred to the oceans in soluble form by precipitation and dry deposition. The stable isotope 9 Be comes from erosion of soils and rocks in the Earth's crust. It is transported by wind and rivers and introduced to the oceans probably in both soluble and insoluble form. 9 Be was measured by atomic absorption spectrometry and 10 Be by A.M.S. The distribution of 10 Be and 9 Be between each phase extracted and the 10 Be/ 9 Be ratios associated were studied in recent marine sediments from Atlantic, Pacific, Indian oceans and Mediterranean sea. The results show that for beryllium the two essential constituent phases of marine sediments are: - the authigenic phase incorporates the soluble beryllium and the detritic phase. The 10 Be/ 9 Be ratio associated with the authigenic fraction varies with location. This suggests that the residence time of beryllium in the soluble phase is lower or comparable to the mixing time of the oceans. The evolution with time of the authigenic 10 Be/ 9 Be ratio is discussed [fr

  12. Isotopic evolution of Mauna Loa volcano

    International Nuclear Information System (INIS)

    Kurz, M.D.; Kammer, D.P.

    1991-01-01

    In an effort to understand the temporal helium isotopic variations in Mauna Loa volcano, we have measured helium, strontium and lead isotopes in a suite of Mauna Loa lavas that span most of the subaerial eruptive history of the volcano. The lavas range in age from historical flows to Ninole basalt which are thought to be several hundred thousand years old. Most of the samples younger than 30 ka in age (Kau Basalt) are radiocarbon-dated flows, while the samples older than 30 ka are stratigraphically controlled (Kahuku and Ninole Basalt). The data reveal a striking change in the geochemistry of the lavas approximately 10 ka before present. The lavas older than 10 ka are characterized by high 3 He/ 4 He (≅ 16-20 times atmospheric), higher 206 Pb/ 204 Pb (≅ 18.2), and lower 87 Sr/ 86 Sr(≅ 0.70365) ratios than the younger Kau samples (having He, Pb and Sr ratios of approximately 8.5 x atmospheric, 18.1 and 0.70390, respectively). The historical lavas are distinct in having intermediate Sr and Pb isotopic compositions with 3 He/ 4 He ratios similar to the other young Kau basalt (≅ 8.5 x atmospheric). The isotopic variations are on a shorter time scale (100 to 10,000 years) than has previously been observed for Hawaiian volcanoes, and demonstrate the importance of geochronology and stratigraphy to geochemical studies. The data show consistency between all three isotope systems, which suggests that the variations are not related to magma chamber degassing processes, and that helium is not decoupled from the other isotopes. However, the complex temporal evolution suggests that three distinct mantle sources are required to explain the isotopic data. Most of the Mauna Loa isotopic variations could be explained by mixing between a plume type source, similar to Loihi, and an asthenospheric source with helium isotopic composition close to MORB and elevated Sr isotopic values. (orig./WL)

  13. Geochemistry of redox-sensitive elements and sulfur isotopes in the high arsenic groundwater system of Datong Basin, China

    International Nuclear Information System (INIS)

    Xie Xianjun; Ellis, Andre; Wang Yanxin; Xie Zuoming; Duan Mengyu; Su Chunli

    2009-01-01

    High arsenic groundwater in the Quaternary aquifers of Datong Basin, northern China contain As up to 1820 μg/L and the high concentration plume is located in the slow flowing central parts of the basin. In this study we used hydrochemical data and sulfur isotope ratios of sulfate to better understand the conditions that are likely to control arsenic mobilization. Groundwater and spring samples were collected along two flow paths from the west and east margins of the basin and a third set along the basin flow path. Arsenic concentrations range from 68 to 670 μg/L in the basin and from 3.1 to 44 μg/L in the western and eastern margins. The margins have relatively oxidized waters with low contents of arsenic, relatively high proportions of As(V) among As species, and high contents of sulfate and uranium. By contrast, the central parts of the basin are reducing with high contents of arsenic in groundwater, commonly with high proportions of As(III) among As species, and low contents of sulfate and uranium. No statistical correlations were observed between arsenic and Eh, sulfate, Fe, Mn, Mo and U. While the mobility of sulfate, uranium and molybdenum is possibly controlled by the change in redox conditions as the groundwater flows towards central parts of the basin, the reducing conditions alone cannot account for the occurrence of high arsenic groundwater in the basin but it does explain the characteristics of arsenic speciation. With one exception, all the groundwaters with As(III) as the major As species have low Eh and those with As(V) have high Eh. Reductive dissolution of Fe-oxyhydroxides or reduction of As(V) are consistent with the observations, however no increase in dissolved Fe concentration was noted. Furthermore, water from the well with the highest arsenic was relatively oxidizing and contained mostly As(V). From previous work Fe-oxyhydroxides are speculated to exist as coatings rather than primary minerals. The wide range of δ 34 S [SO4] values (from

  14. Geochemistry of redox-sensitive elements and sulfur isotopes in the high arsenic groundwater system of Datong Basin, China

    Energy Technology Data Exchange (ETDEWEB)

    Xie Xianjun [MOE Key Laboratory of Biogeology and Environmental Geology and School of Environmental Studies, China University of Geosciences, Wuhan 430074 (China); Ellis, Andre [Department of Geological Sciences, University of Texas at El Paso, TX 79968-0555 (United States); Wang Yanxin, E-mail: yx.wang@cug.edu.cn [MOE Key Laboratory of Biogeology and Environmental Geology and School of Environmental Studies, China University of Geosciences, Wuhan 430074 (China); Xie Zuoming; Duan Mengyu; Su Chunli [MOE Key Laboratory of Biogeology and Environmental Geology and School of Environmental Studies, China University of Geosciences, Wuhan 430074 (China)

    2009-06-01

    High arsenic groundwater in the Quaternary aquifers of Datong Basin, northern China contain As up to 1820 {mu}g/L and the high concentration plume is located in the slow flowing central parts of the basin. In this study we used hydrochemical data and sulfur isotope ratios of sulfate to better understand the conditions that are likely to control arsenic mobilization. Groundwater and spring samples were collected along two flow paths from the west and east margins of the basin and a third set along the basin flow path. Arsenic concentrations range from 68 to 670 {mu}g/L in the basin and from 3.1 to 44 {mu}g/L in the western and eastern margins. The margins have relatively oxidized waters with low contents of arsenic, relatively high proportions of As(V) among As species, and high contents of sulfate and uranium. By contrast, the central parts of the basin are reducing with high contents of arsenic in groundwater, commonly with high proportions of As(III) among As species, and low contents of sulfate and uranium. No statistical correlations were observed between arsenic and Eh, sulfate, Fe, Mn, Mo and U. While the mobility of sulfate, uranium and molybdenum is possibly controlled by the change in redox conditions as the groundwater flows towards central parts of the basin, the reducing conditions alone cannot account for the occurrence of high arsenic groundwater in the basin but it does explain the characteristics of arsenic speciation. With one exception, all the groundwaters with As(III) as the major As species have low Eh and those with As(V) have high Eh. Reductive dissolution of Fe-oxyhydroxides or reduction of As(V) are consistent with the observations, however no increase in dissolved Fe concentration was noted. Furthermore, water from the well with the highest arsenic was relatively oxidizing and contained mostly As(V). From previous work Fe-oxyhydroxides are speculated to exist as coatings rather than primary minerals. The wide range of {delta}{sup 34}S

  15. Petrology and oxygen isotope geochemistry of the Pucon ignimbrite - Southern Andean volcanic zone, Chile: Implications for genesis of mafic ignimbrites

    International Nuclear Information System (INIS)

    McCurry, Michael; Schmidt, Keegan

    2001-01-01

    eruptions were originally dissolved within in the pre-PI magma. They document an important repeating pattern between chemically evolved compositions and explosive eruptions at Volcan Villarrica that is particularly prominent in the cases of the two largest ignimbrite-forming eruptions. They infer that the precursor magma chamber became compositionally stratified through time, with the most evolved, volatile rich magma accumulating towards the top of the chambers, and culminating in voluminous mafic ignimbrite eruptions. In this study we characterize petrologic, geochemical and oxygen isotope characteristics of magmatic pyroclasts from the Pucon Ignimbrite, and one accidental granitoid lithic, extending on the previous work by Clavero (1996) and Lopez-Escobar and Moreno (1995). We critically evaluate previous models, and combine ours and previous data to constrain and develop an alternate petrogenetic model of magmatic evolution of the pre-PI magma chamber, focusing on possible sources of volatiles derived from country rocks and from processes operating within the original magma chamber. We also document the occurrence of a previously unidentified, dacitic, magmatic enclave component of the ignimbrite (au)

  16. Os, Nd and Sr isotope and trace element geochemistry of the Muli picrites: Insights into the mantle source of the Emeishan Large Igneous Province

    Science.gov (United States)

    Li, Jie; Xu, Ji-Feng; Suzuki, Katsuhiko; He, Bin; Xu, Yi-Gang; Ren, Zhong-Yuan

    2010-09-01

    A suite of picrites and basalts from the Muli area, in the northwestern part of the Emeishan continental flood basalt province, provides new and valuable information on the geochemistry of the Emeishan Large Igneous Province (LIP) and its source. The Muli picrites can be classified as type-1 or type-2. The former shows ocean-island basalt-like trace element characteristics, with γ Os (260 Ma) values and ɛ Nd (260 Ma) values ranging from + 7.5 to + 11.5 and from + 6.0 to + 7.8, respectively. This is the first time that picrites with highly radiogenic Os and high Os contents (up to 3.3 ppb) have been recognized in the Emeishan LIP. These characteristics probably reflect a relatively enriched component in the Emeishan LIP source. The type-2 picrites are characterized by non-radiogenic γ Os (260 Ma) values ranging from - 4.2 to - 0.3, and they may be further subdivided into type-2A and type-2B picrites. Type-2A picrites contain moderate amounts of the light rare earth elements (LREEs), have low Ce N/Yb N values (1.1-2.0), and a relatively high initial ɛ Nd (+ 5.0 to + 6.6). In terms of Os and Nd isotopes, the Muli type-2A picrites are similar to the Song Da komatiites of Vietnam and the Gorgona Island picrites, revealing the existence of a depleted mantle component in the Emeishan LIP source. In contrast with the type-2A picrites, type-2B lavas exhibit a negative Nb anomaly and relatively lower initial ɛ Nd and γ Os values (Nb/La > 1.8; ɛ Nd (260 Ma) = - 5.5 to + 6.4; γ Os (260 Ma) = - 4.2 to - 1.9), suggesting that the type-2B lavas have a depleted mantle source, similar to type-2A, but that the type-2B lavas are also influenced by various degrees of mixing of depleted plume-derived melt, sub-continental lithospheric mantle, and/or continental crust. Given that the basalts in the Muli area show similar geochemical features to those of the type-2B picrites, their origins are inferred to be similar.

  17. The chemical conditions of the late Archean Hamersley basin inferred from whole rock and pyrite geochemistry with Δ33S and δ34S isotope analyses

    Science.gov (United States)

    Gregory, Daniel D.; Large, Ross R.; Halpin, Jacqueline A.; Steadman, Jeffery A.; Hickman, Arthur H.; Ireland, Trevor R.; Holden, Peter

    2015-01-01

    The well-preserved late Archean sedimentary rocks of the Fortescue and Hamersley Basins in Western Australia offer fascinating insights into early earth ocean chemistry prior to the Great Oxidation Event (GOE). In this study, we use a combination of whole rock geochemistry, LA-ICPMS trace element analysis of sedimentary pyrite and pyrrhotite and SHRIMP-SI sulfur isotope analyses to elucidate the chemical changes in these sedimentary rocks. These proxies are used to examine chemical conditions of the ocean during the late Archean. Two to three periods of oxygen enrichment prior to the deposition of banded iron formations (BIF) can be identified. One minor stage of general increase in whole rock enrichment factors and trace element content of pyrite is observed up stratigraphy in the Jeerinah Formation, Fortescue Basin and a more substantial stage is present in the Paraburdoo and Bee Gorge Members of the Wittenoom Formation, Hamersley Basin. Some of the trace element enrichments indicate organic matter burial flux (Ni, Cr, Zn, Co and Cu) which suggests an increase in biological productivity. If the increased biological activity reflects an increase in cyanobacteria activity then an associated increase in oxygen is likely to have occurred during the deposition of the Bee Gorge Member. An increase in atmospheric oxygen would result in continental weathering of sulfide and other minerals, increasing the trace element content of the water column via erosion and avoiding excessive depletion of trace elements due to drawdown in seawater. Since some of these trace elements may also be limiting nutrients (such as Mo and Se) for the cyanobacteria, the degree of biological productivity may have further increased due to the increasing amount of trace elements introduced by oxygenation in a positive feedback loop. These periods of increased productivity and oxygen rise stopped prior to the onset of BIF deposition in the Hamersley Basin. This may be due to the ocean reaching an

  18. Determination of rare earth elements, thorium and uranium by inductively coupled plasma mass spectrometry and strontium isotopes by thermal ionization mass spectrometry in soil samples of Bryansk region contaminated due to Chernobyl accident

    International Nuclear Information System (INIS)

    Sahoo, S.K.; Yonehara, H.; Kurotaki, K.; Shiraishi, K.; Ramzaev, V.; Barkovski, A.

    2001-01-01

    Inductively coupled plasma mass spectrometric (ICP-MS) determination of rare earth elements (REEs), thorium and uranium in forest, pasture, field and kitchen garden soils from a Russian territory and in certified reference materials (JLK-1, JSD-2 and BCR-1) is described. In addition to concentration data, strontium isotopic composition of the soil samples were measured by thermal ionization mass spectrometry. The measurements contributed to the understanding of the background levels of these elements in an area contaminated due to Chernobyl accident. There was not a significant variation in the concentration of REEs at different depth levels in forest soil samples, however, the ratio of Th/U varied from 3.32 to 3.60. Though concentration of U and Th varied to some extent, the ratio did not show much variation. The value of 87 Sr/ 86 Sr ratio, was in the top layer soil sample relatively higher than in the lower layers. (author)

  19. 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.

  20. Uranium project. Geochemistry prospection

    International Nuclear Information System (INIS)

    Lambert, J.

    1983-01-01

    Geochemistry studies the distribution of the chemicals elements in the terrestrial crust and its ways to migrate. The terminology used in this report is the following one: 1) Principles of the prospection geochemistry 2) Stages of the prospection geochemistry 3)utility of the prospection geochemistry 4) geochemistry of uranium 5) procedures used within the framework of uranium project 6) Average available 7) Selection of the zones of prospection geochemistry 8) Stages of the prospection, Sample preparation and analisis 9) Presentation of the results

  1. Geochemistry and Nd-isotope systematics of chemical and terrigenous sediments from the Dun Mountain Ophiolite, New Zealand

    International Nuclear Information System (INIS)

    Sivell, W.J.

    2002-01-01

    . Metalliferous contributions to red and green TA in the overlying terrigenous sedimentary sequence also link these facies to early DMOB back-arc eruptives. The red and green TA pass upwards into ungraded Atomodesmid-bearing grey TA, implying turbidite deposition in a shallowing marine environment. The (mainly andesitic) TA show systematic trends of decreasing Eu/Eu* and ε Nd (T) with increasing Ε-REE, La/Y, Th/Sc, and SiO 2 . Th abundances and Th/Sc ratios (up to 1.6) in the TA are akin to those of calc-alkaline magmas in continental arcs, and are significantly greater than island-arc or ophiolitic volcanics. A narrow range of positive ε Nd (T) values (+0.5 to +2.0) for the TA suggests a young differentiated continental arc source, less dissected than the quartzofeldspathic plutonic provenance for the Torlesse (ε Nd (T) N /Yb N = 2.5-2.8) in the sandstones resemble island-arc tholeiites (IAT). The breccias have low Eu/Eu* (c. 0.72), Ce N /Yb N = 1.6, Th/Sc (0.1-0.2), and Tb N /Yb N c. 1.0, features transitional between the sandstones and DMOB plagiogranites. Importantly, the sandstones and breccias show high positive initial Nd ratios (ε Nd (T) = +5 to +8) akin to values for Brook Street IAT (ε Nd (T) = +9). This implies juvenile (mantle-derived) source rocks for both the mafic and felsic younger terrigenous sediments, compatible with crustal residence (mean provenance) ages less than for the TA. Little continental input is permitted by Nd-isotopic data for these rocks. Whereas the early DMOB pillow basalt - chemical sediment - TA assemblage was emplaced in a back-arc setting, with influx of detritus in part from an active continental margin (possibly within the New England Orogen), the younger DMOB terrigenous sediment association shows a close kinship with bimodal DMOB magmatism related to infant arc volcanic centres in an extensional forearc regime. Turbidite sands and mass-flow deposits were shed into proximal fault-bound basins isolated from continental clastic

  2. The hydro- and multi-isotope geochemistry of iron-rich ground waters emerging at the southern Baltic Sea coast line

    Science.gov (United States)

    Lipka, Marko; Wu, Zijun; Escher, Peter; Struck, Ulrich; Dellwig, Olaf; Schafmeister, Maria; Böttcher*, Michael E.

    2013-04-01

    Iron-rich groundwater springs emerging at the shore zone of the southern Baltic Sea (BS; Site Meschendorf) were examined on a seasonal base for a period of about two years. Besides major, minor, and trace elements, stable isotopes of water (H-2, O-18), dissolved inorganic carbon (DIC; C-13), and sulfate (S-34) were analyzed. The stream bed sediment was extracted for the geochemistry of the newly formed precipitates and further characterized via SEM-EDAX. Subsequently, the hydrogeochemical results were subjected to a thermodynamic analysis via the PHREEQC speciation model. The springs emerge from small pits (about 60 cm diameter; up to 15cm depth). Surrounding sediments are sandy with gravels found at depth and corresponding high permeabilities. The positions of different springs on the shore zone were stable during the investigation period while the shape of the pits and the stream beds may vary due to wind- and wave-driven forces. Selected measurements of spring yield discharges close to 10 L/min. The H-2 and O-18 contents of the spring waters indicate the ground water to originate from relatively young mixed meteoric waters. The hydrochemistry of the springs was similar and showed some variability in between which indicates that the genetic processes for the ground water before reaching the surface may slightly differ. The springs are characterized by dissolved Ca, Mg, Na, DIC and sulfate, mainly reflecting the interaction with soils and bedrocks in the recharge area that is dominated by marly till. The oxygen-free ground water is rich in Fe, P, and DIC. Iron and dissolved sulfate originate from the oxidation of pyrite, as further confirmed by the 34-S signature of sulfate. The carbon isotope signature of DIC indicates a mixture of biogenic CO2 from the soil zone with some water-rock interaction with carbonate minerals. The streams flow towards the BS and, in contact with the atmosphere, outgas carbon dioxide and takes up oxygen. Upon CO2-degassing, C-12 is

  3. Rapid determination of strontium-89 and strontium-90 in food and environmental samples by Cerenkov counting

    International Nuclear Information System (INIS)

    Melin, Judith; Suomela, Jorma

    1995-01-01

    The method has been developed for emergency situations. Minimum detectable concentrations of 5 Bq/liter, kilogram of strontium-89 and strontium-90 respectively is achievable in the presence of nuclides considered to be released under accidental conditions. Result on the strontium-89 and strontium-90 content in a sample can be obtained within 12 hours. One technician can easily handle 8-10 samples during a working day of eight hours. The determination of the strontium isotopes is accomplished by monitoring the Cerenkov radiation from strontium-89 and yttrium-90 in a liquid scintillation counter. The latter is the daughter product of strontium-90. Prior to the Cerenkov counting the sample is separated from interfering nuclides by oxalate precipitation, chromate precipitation and HDEHP-extraction. The method has to be further improved and evaluated with respect to different soil types such as forest mineral soil layers, agricultural soils and pastures. Furthermore, the decontamination procedure should be evaluated for a sample containing freshly irradiated uranium. (author)

  4. An overview on geochemistry of Proterozoic massif-type ...

    Indian Academy of Sciences (India)

    A critical study of 311 published WR chemical analyses, isotopic and mineral chemistry of ... Keywords. Massif anorthosite complexes; overview; geochemistry; high-Al gabbro. J. Earth ...... (123–2920 ppm) unlike the experimental results of.

  5. Measurement of strontium-89 and strontium-90 in environmental waters. A tentative reference method

    International Nuclear Information System (INIS)

    1976-03-01

    A tentative reference method for the measurement of 89 Sr and 90 Sr in environmental waters is described. Samples of environmental water sources are collected, preserved with acid-strontium carrier, and analyzed for 89 Sr and/or 90 Sr. The isotopes are separated from the sample water by precipitating with stable strontium carrier as carbonate. The strontium carbonate is dissolved, 90 Sr separated, the strontium reprecipitated as carbonate, filtered, and counted for the combined 89 Sr and 90 Sr activity. The 90 y is allowed to grow in from the 90 y activity; the strontium carbonate is redissolved; the 90 y is separated, precipitated, and counted for the 90 Sr determination. The 89 Sr activity is then determined by difference of the total 89 Sr and 90 y and the separate 90 Sr activities. Recoveries are determined from the added and found (recovered) strontium carrier. Counting efficiencies are determined with prepared standard reference samples. Results are reported in pCi/liter

  6. Geochemical and Pb, Sr, and O isotopic study of the Tiva Canyon Tuff and Topopah Spring Tuff, Yucca Mountain, Nye County, Nevada

    International Nuclear Information System (INIS)

    Neymark, L.A.; Marshall, B.D.; Kwak, L.M.; Futa, Kiyoto; Mahan, S.A.

    1995-01-01

    Yucca Mountain is currently being studied as a potential site for an underground repository for high-level radioactive waste. One aspect of the site characterization studies is an evaluation o the resource potential at Yucca Mountain. Geochemical and isotopic signatures of past alteration of the welded tuffs that underlie Yucca Mountain provide a means of assessing the probability of hydrothermal ore deposits being present within Yucca Mountain. In this preliminary report, geochemical and isotopic measurements of altered Tiva Canyon Tuff and Topopah Spring Tuff collected from fault zones exposed on the east flank of Yucca Mountain and from one drill core are compared to their unaltered equivalents sampled both in outcrop and drill core. The geochemistry and isotopic compositions of unaltered Tiva Canyon Tuff and Topopah Spring Tuff (high-silica rhyolite portions) are fairly uniform; these data provide a good baseline for comparisons with the altered samples. Geochemical analyses indicate that the brecciated tuffs are characterized by addition of calcium carbonate and opaline silica; this resulted in additions of calcium and strontium,increases in oxygen-18 content, and some redistribution of trace elements. After leaching the samples to remove authigenic carbonate, no differences in strontium or lead isotope compositions between altered and unaltered sections were observed. These data show that although localized alteration of the tuffs has occurred and affected their geochemistry, there is no indication of additions of exotic components. The lack of evidence for exotic strontium and lead in the most severely altered tuff samples at Yucca Mountain strongly implies a similar lack of exotic base or precious metals

  7. Lead and strontium isotopic evidence for crustal interaction and compositional zonation in the source regions of Pleistocene basaltic and rhyolitic magmas of the Coso volcanic field, California

    Science.gov (United States)

    Bacon, C.R.; Kurasawa, H.; Delevaux, M.H.; Kistler, R.W.; Doe, B.R.

    1984-01-01

    The isotopic compositions of Pb and Sr in Pleistocene basalt, high-silica rhyolite, and andesitic inclusions in rhyolite of the Coso volcanic field indicate that these rocks were derived from different levels of compositionally zoned magmatic systems. The 2 earliest rhyolites probably were tapped from short-lived silicic reservoirs, in contrast to the other 36 rhyolite domes and lava flows which the isotopic data suggest may have been leaked from the top of a single, long-lived magmatic system. Most Coso basalts show isotopic, geochemical, and mineralogic evidence of interaction with crustal rocks, but one analyzed flow has isotopic ratios that may represent mantle values (87Sr/86Sr=0.7036,206Pb/204Pb=19.05,207Pb/204Pb=15.62,208Pb/204Pb= 38.63). The (initial) isotopic composition of typical rhyolite (87Sr/86Sr=0.7053,206Pb/204Pb=19.29,207Pb/204Pb= 15.68,208Pb/204Pb=39.00) is representative of the middle or upper crust. Andesitic inclusions in the rhyolites are evidently samples of hybrid magmas from the silicic/mafic interface in vertically zoned magma reservoirs. Silicic end-member compositions inferred for these mixed magmas, however, are not those of erupted rhyolite but reflect the zonation within the silicic part of the magma reservoir. The compositional contrast at the interface between mafic and silicic parts of these systems apparently was greater for the earlier, smaller reservoirs. ?? 1984 Springer-Verlag.

  8. Anatomy of a cluster IDP. Part 2: Noble gas abundances, trace element geochemistry, isotopic abundances, and trace organic chemistry of several fragments from L2008#5

    Science.gov (United States)

    Thomas, K. L.; Clemett, S. J.; Flynn, G. J.; Keller, L. P.; Mckay, David S.; Messenger, S.; Nier, A. O.; Schlutter, D. J.; Sutton, S. R.; Walker, R. M.

    1994-01-01

    The topics discussed include the following: noble gas content and release temperatures; trace element abundances; heating summary of cluster fragments; isotopic measurements; and trace organic chemistry.

  9. Marine geochemistry ocean circulation, carbon cycle and climate change

    CERN Document Server

    Roy-Barman, Matthieu

    2016-01-01

    Marine geochemistry uses chemical elements and their isotopes to study how the ocean works. It brings quantitative answers to questions such as: What is the deep ocean mixing rate? How much atmospheric CO2 is pumped by the ocean? How fast are pollutants removed from the ocean? How do ecosystems react to the anthropogenic pressure? The book provides a simple introduction to the concepts (environmental chemistry, isotopes), the methods (field approach, remote sensing, modeling) and the applications (ocean circulation, carbon cycle, climate change) of marine geochemistry with a particular emphasis on isotopic tracers. Marine geochemistry is not an isolated discipline: numerous openings on physical oceanography, marine biology, climatology, geology, pollutions and ecology are proposed and provide a global vision of the ocean. It includes new topics based on ongoing research programs such as GEOTRACES, Global Carbon Project, Tara Ocean. It provides a complete outline for a course in marine geochemistry. To favor a...

  10. Impacts of Dust on Tropical Volcanic Soil Formation: Insights from Strontium and Uranium-Series Isotopes in Soils from Basse-Terre Island, French Guadeloupe

    Science.gov (United States)

    Pereyra, Y.; Ma, L.; Sak, P. B.; Gaillardet, J.; Buss, H. L.; Brantley, S. L.

    2015-12-01

    Dust inputs play an important role in soil formation, especially for thick soils developed on tropical volcanic islands. In these regions, soils are highly depleted due to intensive chemical weathering, and mineral nutrients from dusts have been known to be important in sustaining soil fertility and productivity. Tropical volcanic soils are an ideal system to study the impacts of dust inputs on the ecosystem. Sr and U-series isotopes are excellent tracers to identify sources of materials in an open system if the end-members have distinctive isotope signatures. These two isotope systems are particularly useful to trace the origin of atmospheric inputs into soils and to determine rates and timescales of soil formation. This study analyzes major elemental concentrations, Sr and U-series isotope ratios in highly depleted soils in the tropical volcanic island of Basse-Terre in French Guadeloupe to determine atmospheric input sources and identify key soil formation processes. We focus on three soil profiles (8 to 12 m thick) from the Bras-David, Moustique Petit-Bourg, and Deshaies watersheds; and on the adjacent rivers to these sites. Results have shown a significant depletion of U, Sr, and major elements in the deep profile (12 to 4 m) attributed to rapid chemical weathering. The top soil profiles (4 m to the surface) all show addition of elements such as Ca, Mg, U, and Sr due to atmospheric dust. More importantly, the topsoil profiles have distinct Sr and U-series isotope compositions from the deep soils. Sr and U-series isotope ratios of the top soils and sequential extraction fractions confirm that the sources of the dust are from the Saharan dessert, through long distance transport from Africa to the Caribbean region across the Atlantic Ocean. During the transport, some dust isotope signatures may also have been modified by local volcanic ashes and marine aerosols. Our study highlights that dusts and marine aerosols play important roles in element cycles and

  11. The status of isotopic investigations of the Limpopo mobile belt

    International Nuclear Information System (INIS)

    Barton, J.M. Jr.

    1981-01-01

    The Limpopo Belt is a zone of multiple deformed metamorphic rocks situated between the Rhodesian and Kaapvaal Cratons of Southern Africa. During the duration of the International Geodynamics Project, geochronologic and isotopic investigations were undertaken in the nothern Transvaal of rocks of the Central Zone, Southern Marginal Zone and Soutpansberg Supergroup. Strontium 86, strontium 87 and lead isotopes were used in the isotopic investigations

  12. Strontium isotope systematics of scheelite and apatite from the Felbertal tungsten deposit, Austria - results of in-situ LA-MC-ICP-MS analysis

    Science.gov (United States)

    Kozlik, Michael; Gerdes, Axel; Raith, Johann G.

    2016-02-01

    The in-situ Sr isotopic systematics of scheelite and apatite from the Felbertal W deposit and a few regional Variscan orthogneisses ("Zentralgneise") have been determined by LA-MC-ICP-MS. The 87Sr/86Sr ratios of scheelite and apatite from the deposit are highly radiogenic and remarkably scattering. In the early magmatic-hydrothermal scheelite generations (Scheelite 1 and 2) the 87Sr/86Sr ratios range from 0.72078 to 0.76417 and from 0.70724 to 0.76832, respectively. Metamorphic Scheelite 3, formed by recrystallisation and local mobilisation of older scheelite, is characterised by even higher 87Sr/86Sr values between 0.74331 and 0.80689. Statistics allows discriminating the three scheelite generations although there is considerable overlap between Scheelite 1 and 2; they could be mixtures of the same isotopic reservoirs. The heterogeneous and scattering 87Sr/86Sr ratios of the two primary scheelite generations suggest modification of the Sr isotope system due to fluid-rock interaction and isotopic disequilibrium. Incongruent release of 87Sr from micas in the Early Palaeozoic host rocks of the Habach Complex contributed to the solute budget of the hydrothermal fluids and may explain the radiogenic Sr isotope signature of scheelite. Spatially resolved analyses revealed isotopic disequilibrium even on a sub-mm scale within zoned Scheelite 2 crystals indicating scheelite growth in an isotopic dynamical hydrothermal system. Zoned apatite from the W mineralised Early Carboniferous K1-K3 orthogneiss in the western ore field yielded 87Sr/86Sr of 0.72044-0.74514 for the cores and 0.74535-0.77937 for the rims. Values of magmatic apatite cores from the K1-K3 orthogneiss are comparable to those of primary Scheelite 1; they are too radiogenic to be magmatic. The Sr isotopic composition of apatite cores was therefore equally modified during the hydrothermal mineralisation processes, therefore supporting the single-stage genetic model in which W mineralisation is associated with

  13. Application of organic-geochemistry, coal-petrology and isotope-geochemistry to facies-analysis and hydrocarbon exploration in the NE-Paris Basin (Trias-Lias Luxemburg)

    International Nuclear Information System (INIS)

    Flekken, P.M.

    1978-01-01

    Triassic and Liassic sediments of NE-Paris Basin (Luxemburg) were investigated by organic-geochemical, coal petrographical and isotope-geochemical methods. The objective was to characterize the stratigraphic stages and to investigate the facies relations between them with a view to possible hydrocarbon exploration. The sediments contain an average of 3.1% organic carbon, 413 ug/g extractable organic matter (bitumen) and 0.65% insoluble, isolatable organic particles which constitute part of the kerogen. The non-isolatable kerogen is 2.4% of the whole rock. (orig./BR) [de

  14. Rapid method for the radioactive strontium determination in natural samples; Brza metoda za odredjivanje radioaktivnog stroncija u prirodnim uzorcima

    Energy Technology Data Exchange (ETDEWEB)

    Grahek, Z; Kosutic, K; Lulic, S [Rudjer Boskovic Institute, Zagreb (Croatia)

    1997-12-31

    Radioactive strontium isotopes belong to the group of isotopes that are very dangerous for human health. Therefore radioactive strontium is regularly determined in natural samples. When determining strontium isotopes in natural samples, it is necessary to isolate strontium from the sample because strontium isotopes are pure {beta}-emitters. As natural samples contain much more calcium and sodium than strontium it is necessary to isolate a small quantity of strontium from large sample with simultaneous separation of calcium and other interfering elements. For this purposes an elegant method based on ion exchange chromatography has been developed. Namely, examinations with model system have shown that strontium may be separated from calcium on the column filled with anion exchanger and the mixture of the methanol and nitric acid as eluent. It was also shown that yttrium does not separate from strontium but elutes almost simultaneously with it. Yttrium may be separated from strontium on the column filled with cation exchanger DOWEX 50X8 and nitric acid as eluent. According to the above examinations, the procedure of isolation of strontium and yttrium from natural sample has been created (on assumption that {sup 90}Sr and {sup 90}Y in secular equilibrium in sample). Strontium and yttrium have been isolated from natural sample (standard IAEA A-7) on the column filled with the exchanger AMBERLITE CG-400 and the mixture of methanol and nitric acid as eluent. Strontium and yttrium have been separated on the column with cation exchanger. {sup 90}Sr has been determined through {sup 90}Y by counting the solid yttrium oxalate immediately upon isolation and separation from strontium. {sup 90}Sr has also been determined by counting {sup 90}Sr-{sup 90}Y in secular equilibrium after 15 days. The obtained results of determination of {sup 90}Sr through {sup 90}Y and through secular equilibrium {sup 90}Sr-{sup 90}Y correspond to the declared values of standard. (author). 2 figs., 1

  15. Determination of isotopic composition of strontium in black tea samples from India by Multicollector Inductively Coupled Plasma Mass Spectrometry (MC-ICPMS)

    International Nuclear Information System (INIS)

    Alamelu, D.; Lagad, R.A.; Aggarwal, S.K.; Fang, Kuo Huang; You, Chen-Feng

    2009-01-01

    Identification of geographical origins of food materials is of great importance due to rampant mislabeling that is usually done for getting a higher market price for the agricultural produce. Several works have been undertaken to identify the provenance of tea (Camellia Sinensis). The geographical identification is based on trace elemental profiling of the samples as well as stable isotope ratio signatures. Significant amount of work is also reported for a wide range of food samples such as Coffee, honey, rice etc.

  16. Measurement of strontium isotope ratio in nitric acid extract of peanut testa by ICP-Q-MS after removal of Rb by extraction with pure water.

    Science.gov (United States)

    Zhu, Yanbei; Hioki, Akiharu; Chiba, Koichi

    2014-02-01

    The difference in the distributions of Sr and Rb in peanut seeds was utilized to develop a precise method for Sr isotope ratio measurement by inductively coupled plasma quadruple mass spectrometry (ICP-Q-MS). The testa instead of the whole peanut seed was selected as the sample because apparent enrichment of Sr in comparison to Rb was found in the testa. Furthermore, Rb in the testa was removed by pure water extraction with the aid of sonication to remove the isobaric interference in Sr isotope ratio measurement. The testa taken from one peanut seed was treated as one sample for the analysis. After optimization of the operating conditions, pure water (10 mL for each sample) extraction in 30 min with sonication was able to remove over 95% of Rb in the testa, while after the Rb removal Sr could be completely extracted using 10 mL of 0.3 mol L(-1) HNO3 for each sample. The integration time in ICP-Q-MS measurement was optimized to achieve a lower measurement uncertainty in a shorter time; the results showed that 1s was required and enough for the precise measurement of Sr isotope ratios giving a relative standard uncertainty (n=10) of ca. 0.1%. The present method was applied to peanut seeds grown in Japan, China, USA, India, and South Africa. © 2013 Published by Elsevier B.V.

  17. Behaviour of rare earth elements, thorium, uranium and strontium isotopes in soil samples of Bryansk region contaminated due to Chernobyl accident

    International Nuclear Information System (INIS)

    Sahoo, S.K.; Yonehara, H.; Kurotaki, K.; Shiraishi, K.; Ramzaev, V.; Barkovski, A.

    2000-01-01

    The aim of this study was to characterise the processes which control retention of rare earth elements, U and Th in soil samples of Bryansk region in one of Russian territory contaminated due to Chernobyl accident. Acid sandy and loam sand podzolic soils are typical of this area. We have classified soil samples into forest, pasture, field, yard and kitchen garden. Rare earth elements, U and Th concentrations were measured by digestion soil samples using acid digestion and microwave digestion method followed by ICP-MS whereas Sr isotope ratio ( 87 Sr/ 86 Sr) was determined by using a thermal ionization mass spectrometer (TIMS). In case of forest soil samples, ratio of U/Th varied from 3.32 to 3.60. Though concentration of U and Th varies, ratio does not show much variation. Pasture soil showed higher concentration of REEs, U and Th. Chondrite normalized pattern of soil samples did not differ much from one another excep Ce and Eu and were similar to that for average concentration of continental crust. In case of 87 Sr/ 86 Sr ratio, top layer soil sample shows a relatively higher isotope ratio than lower layers. These data, within the study area, may be reflective of variations in the concentration of elements in reservoir rocks at depth. (author)

  18. Photostriction of strontium ruthenate

    KAUST Repository

    Wei, Tzu-Chiao; Wang, Hsin-Ping; Liu, Heng-Jui; Tsai, Dung-Sheng; Ke, Jr-Jian; Wu, Chung-Lun; Yin, Yu-Peng; Zhan, Qian; Lin, Gong-Ru; Chu, Ying-Hao; He, Jr-Hau

    2017-01-01

    Transition metal oxides with a perovskite crystal structure exhibit a variety of physical properties associated with the lattice. Among these materials, strontium ruthenate (SrRuO3) displays unusually strong coupling of charge, spin and lattice

  19. Geochemistry and petrogenesis of Mesoproterozoic A-type granitoids from the Danish island of Bornholm, southern Fennoscandia

    DEFF Research Database (Denmark)

    Johansson, Åke; Waight, Tod Earle; Andersen, Tom

    2016-01-01

    Granitoids and gneisses from the Danish island of Bornholm have been investigated using whole rock geochemistry, Sr and Nd isotope geochemistry and Hf isotopes in zircon. Recent U–Pb dating shows that the rocks were formed during a short time interval at 1.45 to 1.46 Ga, penecontemporaneous...

  20. Strontium and argon isotopic homogenization of pelitic sediments during low-grade regional metamorphism: the Pan-African Upper Damara Sequence of northern Namibia (South West Africa)

    International Nuclear Information System (INIS)

    Clauer, N.

    1979-01-01

    The fine mineral fractions 0 C and pressures up to 2 kbar. These events are dated at about 535 m.y. and 455 m.y. respectively (with lambda( 87 Rb) = 1.42 X 10 -11 yr -1 ). Anomalously high K-Ar ages on samples from specific stratigraphic horizons can be related to open system behaviour and K migration during the formation of stilpnomelane from ferromagnesian illites. This study shows that age dating of sedimentary rocks subjected to low-grade regional metamorphism can only yield meaningful results if the interpretation of isotopic analyses is based on a clear understanding of the mineralogical processes that led to the formation of these parageneses which characterize the rock unit dated. (Auth.)

  1. Spectroscopic Quadrupole Moments in {96,98}Sr: Evidence for Shape Coexistence in Neutron-Rich Strontium Isotopes at N=60.

    Science.gov (United States)

    Clément, E; Zielińska, M; Görgen, A; Korten, W; Péru, S; Libert, J; Goutte, H; Hilaire, S; Bastin, B; Bauer, C; Blazhev, A; Bree, N; Bruyneel, B; Butler, P A; Butterworth, J; Delahaye, P; Dijon, A; Doherty, D T; Ekström, A; Fitzpatrick, C; Fransen, C; Georgiev, G; Gernhäuser, R; Hess, H; Iwanicki, J; Jenkins, D G; Larsen, A C; Ljungvall, J; Lutter, R; Marley, P; Moschner, K; Napiorkowski, P J; Pakarinen, J; Petts, A; Reiter, P; Renstrøm, T; Seidlitz, M; Siebeck, B; Siem, S; Sotty, C; Srebrny, J; Stefanescu, I; Tveten, G M; Van de Walle, J; Vermeulen, M; Voulot, D; Warr, N; Wenander, F; Wiens, A; De Witte, H; Wrzosek-Lipska, K

    2016-01-15

    Neutron-rich {96,98}Sr isotopes have been investigated by safe Coulomb excitation of radioactive beams at the REX-ISOLDE facility. Reduced transition probabilities and spectroscopic quadrupole moments have been extracted from the differential Coulomb excitation cross sections. These results allow, for the first time, the drawing of definite conclusions about the shape coexistence of highly deformed prolate and spherical configurations. In particular, a very small mixing between the coexisting states is observed, contrary to other mass regions where strong mixing is present. Experimental results have been compared to beyond-mean-field calculations using the Gogny D1S interaction in a five-dimensional collective Hamiltonian formalism, which reproduce the shape change at N=60.

  2. Mantle heterogeneity in northeastern Africa: evidence from Nd isotopic compositions and hygromagmaphile element geochemistry of basaltic rocks from the Gulf of Tadjoura and southern Red Sea regions

    International Nuclear Information System (INIS)

    Barrat, J.A.; Jahn, B.M.; Auvray, B.; Hamdi, H.; Joron, J.L.

    1990-01-01

    Basaltic rocks from the Gulf of Tadjoura and southern Red Sea regions have been analysed for their Nd isotopic compositions and major and trace element concentrations. The wide variation in isotopic and geochemical compositions of the basaltic rocks is best explained by the mixing phenomenon involving a variety of mantle source components. To test the mixing hypothesis, a combined use of Nd isotopes and hygromagmaphile elemental ratios is proven very powerful. Three reservoirs have been identified as minimum components in their petrogenesis: (1) DMM (depleted MORB mantle), a mantle source depleted in light rare earth elements (LREE), which is the principal component of the N-MORB type basalts of this region; (2) REC (Ramad enriched component), equivalent to the hot-spot type of source detected in the south of Red Sea; (3) TEC (Tadjoura enriched component), a rather unique component located in the region of Tadjoura Gulf; it is characterised by a relative depletion in Rb, K, Th and U in a primitive mantle- or chondrite-normalised incompatible element pattern; this component could have been produced by mantle metasomatism of an originally depleted mantle. Mixing in various proportions of the above components is considered to be the principal mechanism for the formation of basalts with such diverse isotopic and trace element compositions. (orig.)

  3. Geochemistry of rare earths and oxygen isotopes in granitic rocks from Monte das Gameleiras and Dona Ines, Rio Grande do Norte-Paraiba border, Brazil

    International Nuclear Information System (INIS)

    Sial, A.N.

    1984-01-01

    The study of oxygen isotopes and rare earth elements in granitic plutons of Monte das Gameleiras and Dona Ines, Rio Grande do Norte-Paraiba border, in Brazil, to define the nature of source rock of progenitor magmas, is presented. (M.C.K.) [pt

  4. The origin and crust/mantle mass balance of Central Andean ignimbrite magmatism constrained by oxygen and strontium isotopes and erupted volumes

    Science.gov (United States)

    Freymuth, Heye; Brandmeier, Melanie; Wörner, Gerhard

    2015-06-01

    Volcanism during the Neogene in the Central Volcanic Zone (CVZ) of the Andes produced (1) stratovolcanoes, (2) rhyodacitic to rhyolitic ignimbrites which reach volumes of generally less than 300 km3 and (3) large-volume monotonous dacitic ignimbrites of up to several thousand cubic kilometres. We present models for the origin of these magma types using O and Sr isotopes to constrain crust/mantle proportions for the large-volume ignimbrites and explore the relationship to the evolution of the Andean crust. Oxygen isotope ratios were measured on phenocrysts in order to avoid the effects of secondary alteration. Our results show a complete overlap in the Sr-O isotope compositions of lavas from stratovolcanoes and low-volume rhyolitic ignimbrites as well as older (>9 Ma) large-volume dacitic ignimbrites. This suggests that the mass balance of crustal and mantle components are largely similar. By contrast, younger (estimated the volume of these ignimbrite deposits throughout the Central Andes during the Neogene and examined the spatiotemporal pattern of so-called ignimbrite flare-ups. We observe a N-S migration of maximum ages of the onset of large-volume "ignimbrite pulses" through time: Major pulses occurred at 19-24 Ma (e.g. Oxaya, Nazca Group), 13-14 Ma (e.g. Huaylillas and Altos de Pica ignimbrites) and 70 km3 Ma-1 km-1 (assuming plutonic/volcanic ratios of 1:5) which are additional to, but within the order of, the arc background magmatic flux. Comparing our results to average shortening rates observed in the Andes, we observe a "lag-time" with large-volume eruptions occurring after accelerated shortening. A similar delay exists between the ignimbrite pulses and the subduction of the Juan Fernandez ridge. This is consistent with the idea that large-volume ignimbrite eruptions occurred in the wake of the N-S passage of the ridge after slab steepening has allowed hot asthenospheric mantle to ascend into and cause the melting of the mantle wedge. In our model, the

  5. Water-Rock Interactions in the Peridotite Aquifer of the Oman-UAE Ophiolite: Strontium Isotopic Ratio and Geochemical Evolution of Groundwater

    Science.gov (United States)

    Bompard, Nicolas; Matter, Juerg; Teagle, Damon

    2016-04-01

    The peridotite aquifer in Wadi Tayin, Sultanate of Oman, is a perfect example of natural carbonation of ultramafic rocks. In situ mineral carbonation is considered the most safest and permanent option of CO2 Capture and Sequestration (CCS). However, the process itself is yet to be characterised and a better understanding of the mechanisms involved in natural mineral carbonation is needed before geo-engineering it. We used the 87Sr/86Sr system to follow the water-rock interactions along the groundwater flowpath in the peridotite aquifer and to determine the sources of divalent cations (Mg2+, Ca2+) required for mineral carbonation. The Sr-isotope data of groundwater show that the aquifer rocks are the main source for divalent cations (Mg2+, Ca2+ and Sr2+) and secondary carbonates are their main sink. The groundwater 87Sr/86Sr ratio evolves with its pH: from 87Sr/86Sr = 0.7087 (n=3) to 0.7082 (n=8) between pH 7 and 8, and from 0.7086 (n=6) at pH 9 to 0.07075 (n=9) at pH 11. This evolution seems to support a two-step model for the water-rock interactions in the peridotite aquifer. From pH 7 to 8, secondary Ca-carbonate precipitation buffers the pH rise resulting from peridotite serpentinisation. From pH 9 to 11, peridotite serpentinisation drives the pH to alkaline condition. The change from a Mg-rich to a Ca-rich groundwater at pH 9 seems to confirm the two-step model.

  6. Hydrochemistry and isotope geochemistry as management tools for groundwater resources in multilayer aquifers: A study case from the Po plain (Lomellina, South-Western Lombardy, Italy)

    Energy Technology Data Exchange (ETDEWEB)

    Pilla, G; Sacchi, E; Ciancetti, G; Braga, G [Dipartimento di Scienze della Terra, Universita di Pavia, Pavia (Italy); Zuppi, G M [Dipartimento di Scienze Ambientali, Universita Ca' Foscari di Venezia, Venice (Italy)

    2003-07-01

    Full text: The Po plain, located in Northern Italy, hosts a multi-layer alluvial aquifer of Quaternary age constituted by sands interbedded with clays. The plain supports most of the agricultural and industrial activities of Northern Italy, which are associated with groundwater pollution in the shallower portions of the aquifer. The increasing demand of water for industrial and domestic use has led to the exploitation of deeper layers of the aquifer, without a rational management of the resource. Only in the last decade, the government agencies have started a global evaluation of the quality standards of pumped groundwater, urged by the increasing need for clean water for domestic use. The task is particularly difficult because of missing or approximate well logs and the presence of multi-filter wells tapping in different aquifers. In this case the chemical and isotopic characterisation of groundwaters is the only reliable tool to reconstruct the geometry, the interconnections and the characteristics of the aquifers. This study, promoted by the local agency for groundwater management and protection (Amministrazione Provinciale di Pavia, settore tutela e valorizzazione ambientale - U.O.C. Acqua) focused on a limited portion of the Po plain, the Lomellina region, of approximately 900 km{sup 2}. The region is bound to the South by the Po river, to the East and West by the Sesia and the Ticino rivers respectively, and to the North by the administrative boundary. The study aimed at the hydrogeological, hydrochemical and isotopic characterisation of the aquifers, allowing to serve as basis for the correct management of the groundwater resource. A preliminary reconstruction of the hydrogeological asset of the Lomellina plain was performed through the analysis of the stratigraphic data from 102 municipal wells. On this basis, a shallow phreatic aquifer, reaching depths of about 50-60 m from the surface, and two groups of aquifers containing confined groundwater, were

  7. Optical lattice clock with strontium atoms; Horloge a reseau optique a atomes de strontium

    Energy Technology Data Exchange (ETDEWEB)

    Baillard, X.; Le Targat, R.; Fouche, M.; Brusch, A.; Westergaard, Ph.G.; Lecallier, A.; Lodewyck, J.; Lemonde, P. [Observatoire de Paris, LNE-SYRTE, Systemes de Reference Temps Espace, 75 (France)

    2009-07-01

    Optical lattice clocks, which were first imagined in 2000, should allow one to achieve unprecedented performances in the domain of atomic clocks. We present here the Strontium lattice clock, developed at LNE-SYRTE. The principle, in particular trapping atoms in the Lamb-Dicke regime and the notion of magic wavelength, is first explained. We then present the results obtained for the {sup 87}Sr isotope, with a frequency accuracy of 2,6.10{sup -15}, and the {sup 88}Sr isotope, with. which we perform the first frequency measurement of an optical lattice clock with bosonic atoms. (authors)

  8. Strontium-82/rubidium-82 generator

    International Nuclear Information System (INIS)

    Gennaro, G.P.; Haney, P.S.

    1986-01-01

    Hydroxylapatite, a compound having the formula: M 10 (PO 4 ) 6 (OH) 2 wherein M is calcium, strontium, barium, lead, iron, sodium, potassium, zinc, cadmium, magnesium, aluminium or a rare earth metal, is provided as a support medium for strontium-82 in a strontium-82/rubidium-82 parent-daughter radionuclide generator

  9. Slab-derived components in the subcontinental lithospheric mantle beneath Chilean Patagonia: Geochemistry and Sr-Nd-Pb isotopes of mantle xenoliths and host basalt

    Science.gov (United States)

    Jalowitzki, Tiago; Gervasoni, Fernanda; Conceição, Rommulo V.; Orihashi, Yuji; Bertotto, Gustavo W.; Sumino, Hirochika; Schilling, Manuel E.; Nagao, Keisuke; Morata, Diego; Sylvester, Paul

    2017-11-01

    In subduction zones, ultramafic xenoliths hosted in alkaline basalts can yield significant information about the role of potential slab-derived components in the subcontinental lithospheric mantle (SCLM). Chemical and isotopic heterogeneities in such xenoliths are usually interpreted to reflect melt extraction followed by metasomatic re-enrichment. Here we report new whole-rock major, trace element and isotopic (Sr-Nd-Pb) data for a Proterozoic suite of 17 anhydrous spinel-lherzolites and Eocene (new K-Ar data) host alkaline basalt found near Coyhaique ( 46°S), Aysén Region, Chile. These Patagonian nodules are located in a current back-arc position, 100 km east of the present day volcanic arc and 320 km from the Chile Trench. The mantle xenoliths consist of coarse- to medium-grained spinel-lherzolites with trace element compositions characteristic of a subduction zone setting, such as pronounced negative Nb, Ta and Ti anomalies coupled with significant enrichment of LILEs (e.g., U) and chalcophile elements (W, Pb and Sn). Most of them are characterized by flat to depleted light-rare earth element (LREE) patterns (Ce/YbN = 0.6-1.1) coupled with less radiogenic Sr-Pb (87Sr/86Sr = 0.702422-0.703479; 206Pb/204Pb = 18.212-18.539) and more radiogenic Nd isotopic compositions (143Nd/144Nd = 0.512994-0.513242), similar to the depleted mantle component (DMM or PREMA). In contrast, samples with slight LREE enrichment (Ce/YbN = 1.3-1.8) show more radiogenic Sr-Pb (87Sr/86Sr = 0.703791-0.704239; 206Pb/204Pb = 18.572-18.703) and less radiogenic Nd isotopic compositions (143Nd/144Nd = 0.512859-0.512934), similar to the EM-2 reservoir. These new geochemical and isotope data suggest that the Coyhaique spinel-lherzolites are derived from a heterogeneous SCLM resulting from mixing between a depleted mantle component and up to 10% of slab-derived components. The enriched component added to the SCLM represents variable extents of melts of both subducted Chile Trench sediments and

  10. Problems of applied geochemistry

    Energy Technology Data Exchange (ETDEWEB)

    Ovchinnikov, L N

    1983-01-01

    The concept of applied geochemistry was introduced for the first time by A. Ye. Fersman. He linked the branched and complicated questions of geochemistry with specific problems of developing the mineral and raw material base of our country. Geochemical prospecting and geochemistry of mineral raw materials are the most important sections of applied geochemistry. This now allows us the right to view applied geochemistry as a sector of science which applies geochemical methodology, set of geochemical methods of analysis, synthesis, geological interpretation of data based on laws governing theoretical geochemistry to the solution of different tasks of geology, petrology, tectonics, stratigraphy, science of minerals and other geological sciences, and also the technology of mineral raw materials, interrelationships of man and nature (ecogeochemistry, technogeochemistry, agrogeochemistry). The main problem of applied geochemistry, geochemistry of ore fields is the prehistory of ore formation. This is especially important for metallogenic and forecasting constructions, for an understanding of the reasons for the development of fields and the detection of laws governing their distribution, their genetic links with the general geological processes and the products of these processes.

  11. Petrography and stable isotope geochemistry of Oligocene-Miocene continental carbonates in south Texas: Implications for paleoclimate and paleoenvironment near sea-level

    Science.gov (United States)

    Godfrey, Conan; Fan, Majie; Jesmok, Greg; Upadhyay, Deepshikha; Tripati, Aradhna

    2018-05-01

    Cenozoic sedimentary rocks in the southern Texas Gulf Coastal Plains contain abundant continental carbonates that are useful for reconstructing terrestrial paleoclimate and paleoenvironment in a region near sea-level. Our field observations and thin section characterizations of the Oligocene and Miocene continental carbonates in south Texas identified three types of pedogenic carbonates, including rhizoliths, carbonate nodules, and platy horizons, and two types of groundwater carbonates, including carbonate-cemented beds and carbonate concretions, with distinctive macromorphologic and micromorphologic features. Based on preservations of authigenic microfabrics and variations of carbon and oxygen isotopic compositions, we suggest these carbonates experienced minimal diagenesis, and their stable isotopic compositions reflect paleoclimate and paleoenvironment in south Texas. Our Oligocene and Miocene carbonate clumped isotope temperatures (T(Δ47)) are 23-28 °C, slightly less than or comparable to the range of modern mean annual and mean warm season air temperature (21-27 °C) in the study area. These T(Δ47) values do not show any dependency on carbonate-type, or trends through time suggesting that groundwater carbonates were formed at shallow depths. These data could indicate that air temperature in south Texas was relatively stable since the early Oligocene. The reconstructed paleo-surface water δ18O values are similar to modern surface water which could indicate that meteoric water δ18O values also remained stable since the early Oligocene. Mean pedogenic carbonate δ13C values increased - 4.6‰ during the late Miocene, most likely reflecting an expansion of C4 grassland in south Texas. This study provides the first mid- and late Cenozoic continental records of paleoclimate and paleoecology in a low-latitude, near sea-level region.

  12. Ecophysiology of the hydrothermal vent snail Ifremeria nautilei and barnacle Eochionelasmus ohtai manusensis, Manus Basin, Papua New Guinea: Insights from shell mineralogy and stable isotope geochemistry

    Science.gov (United States)

    Bojar, Ana-Voica; Lécuyer, Christophe; Bojar, Hans-Peter; Fourel, François; Vasile, Ştefan

    2018-03-01

    Deep-sea vent communities live on a limited area characterized by sharp physico-chemical (temperature, salinity, pH) gradients. Around the vent, the fauna is distributed accordingly, showing characteristic niche partitioning for different groups of animals. In this study we investigate shell microstructure, minor elements and stable isotope compositions of two groups of organisms such as a snail, Ifremeria nautilei, and a crustacean, Eochionelasmus ohtai manusensis. Both organisms occupy distinct niches within the same hydrothermal vent field of the Manus Basin, Western Pacific. Powder XRD and electron microbeam analysis of a polished cross-section indicate that the shells are composed of microcrystalline calcite, with distinct Na, Mg, Sr, and S element contents. For both specimens 20-30 μm large weddellite crystals were found. The δ18O profiles were obtained perpendicular to the growth increments of I. nautilei and E. o. manusensis calcitic shells. Those profiles reveal isotopic variations of 0.5 and 0.6‰, respectively for both intra- and inter-shell measurements. For E. o. manusensis, the Mg content suggests continuous shell growth during the year, both δ18O and Mg data supporting cyclical variation of temperature at vent site. The calculated temperatures at sites with I. nautilei and E. o. manusensis range from 17° to 21.5°C and from 2.1° to 7.2°C, respectively, showing a similar variability of 5-6 °C. The δ13C values of the Ifremeria calcitic shell range from 3‰ to 4.6‰ (V-PDB), the isotopic composition being 13C-enriched relative to the surrounding inorganic pool. The δ13C values of the chitine layer covering the shell range from - 33 to - 31.1‰. The δ13C values of Eochionelasmus vary between 0‰ and 1‰, reflecting the surrounding inorganic DIC pool.

  13. Pb/Pb isochron ages and Pb isotope geochemistry of Bambui Group carbonate rocks from the southern portion of the Sao Francisco Basin

    International Nuclear Information System (INIS)

    Babinski, M.

    1993-01-01

    This study involves the establishment of chemical and analytical procedure for Pb/Pb dating of Neo proterozoic carbonate rocks and their application to obtaining isochron ages of Bambui Group rocks from the southern portion of the Sao Francisco Basin, Minas Gerais State. The Pb isotopic compositions and U and Pb concentrations determined on more than 90 samples (≅ 600 analyses) from Sete Lagoas do Jacare formations, Bambui Group, from different parts of the basin, showed four distinct types of Pb, here called types I, II, III and IV. Type I Pb was found in samples with low Pb concentrations and relatively high U concentrations. Type II Pb is present in samples with relatively high Pb concentrations and low U concentrations it is non-radiogenic crustal Pb. Type III Pb is also found in samples with high Pb concentrations and low U concentrations but it is radiogenic crustal Pb. Type IV Pb occurs in samples with U/Pb ratios lower than 1 and is intermediate in composition between Type III and Type I Pb. According to the data presented in this paper it is suggested that carbonate rocks from Sete Lagoas Formations were deposited before 686±69 Ma. Rocks from the Lagoa do Jacare Formation, contained only Type II Pb, which does not permit determination of a Pb/Pb age. During the interval from 690 to 500 Ma, the Pb isotope system of the carbonate rocks from the Sao Francisco Basin was disturbed, and in some areas it was totally reset. The imprecise U/Pb ages of 550-600 Ma obtained from some of the carbonate rocks reflect this disturbance. The ages determined in this study are in agreement with most of the published ages of the tectonism from the Brasiliano fold belts marginal to Sao Francisco Craton, showing that the isotopic systems of Sao Francisco Basin rocks were largely affected by brasiliano tectonism. (author)

  14. 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

    International Nuclear Information System (INIS)

    Luck, J.M.; Othman, D.B.

    1997-01-01

    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

  15. Strontium-90 accumulation in fowl and its migration into egg following chromic intake with forage

    International Nuclear Information System (INIS)

    Koldaeva, K.A.; Sarapul'tsev, I.A.

    1975-01-01

    Accumulation of strontium-90 in different organs of hens and its transfer ot eggs have been studied at chronic feeding with the isotope. The feed consisted of potato and wheat grown on plots artificially contaminated with strontium-90. The duration of the experiment is 30 days during which the hens lay 35 eggs. Strontium-90 and calcium are determined in the femur, shoulder, breastbone, skull, rib, vertebrae, and muscles. Determination errors do not exceed 10 and 5% for the isotope and calcium respectively. Concentration of stronium-90 and calcium in different bones and in muscles of laying hens and roosters after a month's feeding with the isotope presented. The isotope concentration in bones of hens 3 to 4 times higher than in bones of roosters while the muscle concentration is similar in both cases. The higher content of strontium-90 per g of bone tissue calcium in hens can be explained by a higher level of calcium metabolism during the laying period. Data on strontium-90 and calcium concentration in eggs are also presented. The bulk of the isotope accumulates in the eggshell (96.4%). One egg contains an average of 31% of the daily strontium intake

  16. Strontium-90 (90Sr) determination using liquid scintillation counting

    International Nuclear Information System (INIS)

    Cheberle, L.T.V.; Rosa, M.M.L.; Ferreira, M.T.; Taddei, M.H.T.

    2015-01-01

    This procedure describes a method for separation and measurement of strontium 90 Sr in water, soils, and biological samples. Water samples may be concentrated using evaporation or calcium phosphate coprecipitation. Soils and biological materials must be dissolved using wet digestion. Tracers and carriers must be added before the attack. Radioactive strontium is separated employing a specific resin before determination by liquid scintillation counting using the double energetic window method. The resin is used to concentrate strontium from samples. Stable strontium is used to monitor method yields and correct results to improve precision and accuracy. The presence of elemental strontium in the sample may bias the gravimetric yield determination. If it is suspected that natural strontium is present in the sample, its concentration should be determined by a suitable means (ICP), and the yield calculation properly modified. Sr-Spec resin with an 8M HNO 3 load solution is used to effectively remove 140 Ba and 40 K isotopes, as well as other interferences from the matrix. Tetravalent plutonium, neptunium, cerium and ruthenium, however, are not removed using nitric acid. The radiochemical procedure was tested using PROCORAD intercomparison exercises and PNI samples. (author)

  17. Accumulation of strontium 90 and cesium 137 in some hydrobionts

    International Nuclear Information System (INIS)

    Boyadzhiev, A.; Keslev, D.; Kerteva, A.; Novakova, E.

    1974-01-01

    Factors responsible for the accumulation of strontium 90 and cesium 137 in some plant organisms, characteristic for fishes in Bulgarian fresh-water reservoirs and in Black Seawater, were examined. The investigated samples were taken during spring, summer and autumn-winter seasons 1967/1968. Each sample burnt to ashes at 450 0 C was examined for strontium 90 and cesium 137 content as well as stable isotopes of calcuim and potassium. Accumulation factors for strontium 90 and cesium 137 were significantly higher in freshwater hydrobionts than in seawater hydrobionts. This could be explained by variations in the concentration of stable isotopes of calcium and potassium from freshwater reservoirs and from seawater. Potassium and calcium concentrations were relatively constant in seawater while in freshwater they were significantly variable. Accumulation factors for these radionuclides increased according to the amount of rain and the altitude above sea level. Strontium 90 was deposited mostly in fins, less in scales and least in the meat of fishes; cesium 137 was mainly deposited in the meat and less in the other parts of fishes. The highest accumulation factors for strontium 90 were determined in fishes and for cesium 137 in plant organisms. The most convenient plant and fish species for tracing radioactive contamination of freshwater reservoirs and in the Black Sea were indicated. (A.B.)

  18. Gas composition and isotopic geochemistry of cuttings, core, and gas hydrate from the JAPEX/JNOC/GSC Mallik 2L-38 gas hydrate research well

    Science.gov (United States)

    Lorenson, T.D.

    1999-01-01

    Molecular and isotopic composition of gases from the JAPEX/JNOC/GSC Mallik 2L-38 gas hydrate research well demonstrate that the in situ gases can be divided into three zones composed of mixtures of microbial and thermogenic gases. Sediments penetrated by the well are thermally immature; thus the sediments are probably not a source of thermogenic gas. Thermogenic gas likely migrated from depths below 5000 m. Higher concentrations of gas within and beneath the gas hydrate zone suggest that gas hydrate is a partial barrier to gas migration. Gas hydrate accumulations occur wholly within zone 3, below the base of permafrost. The gas in gas hydrate resembles, in part, the thermogenic gas in surrounding sediments and gas desorbed from lignite. Gas hydrate composition implies that the primary gas hydrate form is Structure I. However, Structure II stabilizing gases are more concentrated and isotopically partitioned in gas hydrate relative to the sediment hosting the gas hydrate, implying that Structure II gas hydrate may be present in small quantities.

  19. Pre-Hercynian hydrothermalism in South Iberia: lead isotope geochemistry constraints; Hydrothermalisme ante-hercynien en Sud-Iberie: apport de la geochimie isotopique du plomb

    Energy Technology Data Exchange (ETDEWEB)

    Marcoux, E.; Onezime, J. [Orleans Univ., Institut des Sciences de la Terre d' Orleans, 45 (France); Pascual, E. [Universite d' Huelva, Dept. de Geologia y MIneria, Huelva (Spain)

    2002-04-01

    Lead isotope study has been performed on massive sulphide deposits of Ossa-Morena and Aracena Belt (South Iberia). Results suggest the existence of at least two ancient hydrothermal events. The first one, Upper Brioverian in age ({approx}600-570 Ma), gave birth to Maria-Luisa and Puebla de la Reina massive sulphide deposits; it thus confirms the existence of a Cadomian orogen in South Iberia. Isotopic compositions indicate a local contribution of mantle-derived material (Maria Luisa mine), confirming the presence of ancient oceanic crust in Aracena Belt. This mineralizing event seems to extend till the Armorican Massif. The second episode, Eo-Hercynian in age ({approx}400-350 Ma) has allowed genesis of massive sulphide deposits of la Nava Paredon and Aguas Blancas, and could be coeval with the emplacement of South-Iberian massive sulphide ore deposits in the neighbouring South-Portuguese Zone. A more continental crustal source for later ore deposits could explain the much more important metal accumulation in this zone. (authors)

  20. Geochemistry, Nd-Pb Isotopes, and Pb-Pb Ages of the Mesoproterozoic Pea Ridge Iron Oxide-Apatite–Rare Earth Element Deposit, Southeast Missouri

    Science.gov (United States)

    Ayuso, Robert A.; Slack, John F.; Day, Warren C.; McCafferty, Anne E.

    2016-01-01

    Iron oxide-apatite and iron oxide-copper-gold deposits occur within ~1.48 to 1.47 Ga volcanic rocks of the St. Francois Mountains terrane near a regional boundary separating crustal blocks having contrasting depleted-mantle Sm-Nd model ages (TDM). Major and trace element analyses and Nd and Pb isotope data were obtained to characterize the Pea Ridge deposit, improve identification of exploration targets, and better understand the regional distribution of mineralization with respect to crustal blocks. The Pea Ridge deposit is spatially associated with felsic volcanic rocks and plutons. Mafic to intermediate-composition rocks are volumetrically minor. Data for major element variations are commonly scattered and strongly suggest element mobility. Ratios of relatively immobile elements indicate that the felsic rocks are evolved subalkaline dacite and rhyolite; the mafic rocks are basalt to basaltic andesite. Granites and rhyolites display geochemical features typical of rocks produced by subduction. Rare earth element (REE) variations for the rhyolites are diagnostic of rocks affected by hydrothermal alteration and associated REE mineralization. The magnetite-rich rocks and REE-rich breccias show similar REE and mantle-normalized trace element patterns.Nd isotope compositions (age corrected) show that: (1) host rhyolites have ɛNd from 3.44 to 4.25 and TDM from 1.51 to 1.59 Ga; (2) magnetite ore and specular hematite rocks display ɛNd from 3.04 to 4.21 and TDM from 1.6 to 1.51 Ga, and ɛNd from 2.23 to 2.81, respectively; (3) REE-rich breccias have ɛNd from 3.04 to 4.11 and TDM from 1.6 to 1.51 Ga; and (4) mafic to intermediate-composition rocks range in ɛNd from 2.35 to 3.66 and in TDM from 1.66 to 1.56. The ɛNd values of the magnetite and specular hematite samples show that the REE mineralization is magmatic; no evidence exists for major overprinting by younger, crustal meteoric fluids, or by externally derived Nd. Host rocks, breccias, and

  1. Isotopic and trace element geochemistry of the Seligdar magnesiocarbonatites (South Yakutia, Russia): Insights regarding the mantle evolution beneath the Aldan-Stanovoy shield

    Science.gov (United States)

    Doroshkevich, Anna G.; Prokopyev, Ilya R.; Izokh, Andrey E.; Klemd, Reiner; Ponomarchuk, Anton V.; Nikolaeva, Irina V.; Vladykin, Nikolay V.

    2018-04-01

    The Paleoproterozoic Seligdar magnesiocarbonatite intrusion of the Aldan-Stanovoy shield in Russia underwent extensive postmagmatic hydrothermal alteration and metamorphic events. This study comprises new isotopic (Sr, Nd, C and O) data, whole-rock major and trace element compositions and trace element characteristics of the major minerals to gain a better understanding of the source and the formation process of the carbonatites. The Seligdar carbonatites have high concentrations of P2O5 (up to 18 wt%) and low concentrations of Na, K, Sr and Ba. The chondrite-normalized REE patterns of these carbonatites display significant enrichments of LREE relative to HREE with an average La/Ybcn ratio of 95. Hydrothermal and metamorphic overprints changed the trace element characteristics of the carbonatites and their minerals. These alteration processes were responsible for Sr loss and the shifting of the Sr isotopic compositions towards more radiogenic values. The altered carbonatites are further characterized by distinct 18O- and 13C-enrichments compared to the primary igneous carbonatites. The alteration most likely resulted from both the percolation of crustal-derived hydrothermal fluids and subsequent metamorphic processes accompanied by interaction with limestone-derived CO2. The narrow range of negative εNd(T) values indicates that the Seligdar carbonatites are dominated by a homogenous enriched mantle source component that was separated from the depleted mantle during the Archean.

  2. Barren Miocene granitoids in the Central Andean metallogenic belt, Chile: Geochemistry and Nd-Hf and U-Pb isotope systematics

    International Nuclear Information System (INIS)

    Deckart, Katja; Godoy, Estanislao; Bertens, Alfredo; Jerez, Daniela; Saeed, Ayesha

    2010-01-01

    Four Middle-to-Late Miocene barren plutonic complexes that occur between the giant porphyry copper deposits of the central Chilean Andes were selected for U-Pb LA-ICPMS geochronology and Hf-isotope systematics on single zircon grains. Major and trace elements and Sr-Nd-Hf isotope whole rock geochemical studies were undertaken to compare with slightly younger or coeval barren and fertile intrusive rocks between 32 o and 34 o S. The studied granitoids yield resolvable crystallization ages of 11.3±0.1 Ma (Cerro Meson Alto massif), 10.3±0.2 Ma (La Gloria pluton), 14.9±0.2 Ma/14.9±0.1 Ma (Yerba Loca stock) and 11.2±0.1 Ma/14.7±0.1 Ma (San Francisco Batholith). Major and trace elements discard an adakitic signature as suggested for coeval porphyric intrusions at 32 o S, slightly younger mineralized porphyries at Rio Blanco-Los Bronces deposit and other Cenozoic adakites. Volcanic host rocks are less fractionated than the intrusive rock units. The same observation can be made for the unmineralized northern plutons compared to the southern ones. Initial Sr-Nd isotope data show insignificant variation (0.703761-0.704118 and 0.512758- 0.512882), plotting in the mantle array. Trace element enrichment can be explained by addition of subducted-slab fluids and/or terrigenous sediments to the mantle wedge prior to and/or slight crustal input during magma ascent. Zircon grains separated from these barren intrusives share a similar initial εHf-data variation for the younger age group (10-12 Ma; 7.04-9.54) and show a more scattered range for the older one (14-15 Ma; 8.50-15.34); both sets plot between the DM and CHUR evolution lines. There is evidence that magma evolution was slightly distinct through time from older to younger barren magmatism, compared to a few fertile porphyritic rocks from Rio Blanco-Los Bronces porphyry copper deposit. It is suggested that chronological inconsistencies within these complexes might be related to differential shortening across the NE

  3. POTENTIALLY TOXIC ELEMENT CYCLES AND CHARACTERIZATION OF MULTIPLE SOURCES IN THE IRRIGATION DITCHES FROM THE RAVENNA COASTAL PLAIN THROUGH TRACE ELEMENTS AND ISOTOPE GEOCHEMISTRY

    Directory of Open Access Journals (Sweden)

    Livia Vittori Antisari

    2010-04-01

    Full Text Available While monitoring the physico-chemical characteristics, trace elements and O-H-Sr-B isotopic data were obtained in superficial waters from a number of irrigations canals and ditches in the Ravenna coastal plain, in order to highlight the cycling of potentially toxic elements and the different sources of the solutes. Surveys were conducted during March and July 2008, and considered as representative of the waters in winter and summer, respectively. In summer, the water mass balance in the network is mostly controlled by the ingression of freshwaters from the Canale Emiliano Romagnolo (CER. The O-H isotopic data indicated that, in winter, waters are primarily recharged from Apennine catchments and undergo evaporation to different extents.The boron isotopic signature indicates the important role played by the marine component. A major seawater contribution was evidenced in canals close to the coastline; however, the process controlling the origin of dissolved boron is not solely related to direct mixing with sea water but comprises an additional source probably related to water-soil exchanges and boron of marine origin leaching, owing to the prolonged exposure of alluvial sediments to sea water. An additional boron contribution from the agricultural practice was is also evidenced. Calculation based on the conservative behaviour of chloride ions indicated that in canals and ditches not directly connected with the sea up to the 80% of the Sr budget did not originate from seawater, indicating a source from Al-silicate minerals and supporting the hypothesis of significant soil-water interactions and chemical exchanges.The positive correlation between pH and dissolved oxygen in winter waters is likely to reflect CO2 consumption during algal photosynthesis, favouring the in-situ generation of colloidal particles due to the oxidative precipitation of ferric iron oxy-hydroxides and probably small carbonate particles able to adsorb trace metals on their

  4. Geochemistry, U-Pb SHRIMP zircon dating and Hf isotopes of the Gondwanan magmatism in NW Argentina: petrogenesis and geodynamic implications

    International Nuclear Information System (INIS)

    Poma, Stella; Zappettini, Eduardo O; Quenardelle, Sonia; Santos, Joao O; Koukharsky, Magdalena; Belousova, Elena; McNaughton, Neil

    2014-01-01

    We have carried out zircon U-Pb SHRIMP dating and Hf isotope determinations as well as geochemical analyses on three plutonic units of Gondwanan magmatism that crop out in NW Argentina. Two episodes of different age and genesis have been identified. The older one includes gabbros and diorites (Rio Grande Unit) of 267±3 Ma and granitoids (belonging to the Llullaillaco Unit) of 263±1 Ma (late Permian, Guadalupian); the parent magmas were generated in an intraplate environment and derived from an enriched mantle but were subsequently contaminated by crustal components. The younger rocks are granodiorites with arc signature (Chuculaqui Unit) and an age of 247±2 Ma (middle Triassic-Anisian). Hf isotope signature of the units indicates mantle sources as well as crustal components. Hf model ages obtained are consistent with the presence of crustal Mesoproterozoic (mainly Ectasian to Calymnian (T DM(c) =1.24 to 1.44 Ga-negative ε Hf m) and juvenile Cryogenian sources (T DM =0.65 to 0.79 Ga-positiveε Hf(T) , supporting the idea of a continuous, mostly Mesoproterozoic, basement under the Central Andes, as an extension of the Arequipa-Antofalla massif. The tectonic setting and age of the Gondwanan magmatism in NW Argentina allow to differentiate: a. Permian intra-plate magmatism developed under similar conditions to the upper section of the Choiyoi magmatism exposed in the Frontal Cordillera and San Rafael Block, Argentina; b. Triassic magmatism belonging to a poorly known subduction-related magmatic arc segment of mostly NS trend with evidence of porphyry type mineralization in Chile, allowing to extend this metallotect into Argentina

  5. Nd, Sr-isotopic provenance and trace element geochemistry of Amazonian foreland basin fluvial sands, Bolivia and Peru: Implications for ensialic Andean orogeny

    International Nuclear Information System (INIS)

    Basu, A.R.; Sharma, M.; DeCelles, P.G.

    1990-01-01

    Nd and Sr isotopes and the trace element contents, including the rare earths, were determined for fluvial sands of lithic arenite composition from the Madre de Dios foreland basin of Bolivia and Peru. On standard petrologic ternary diagrams, the sands fall in the recycled orogen provenance field and thus are similar to typical ancient foreland basin composition. The average rare earth elemental pattern of the sands is identical to the upper continental crustal average, as estimated from post-Archean composite shales of different continents. Ratio of Th/U, Co/Th, La/Sc and Th/Sc of the fluvial sands are intermediate between an average magmatic arc and an upper crustal average compositions. The dispersion of some trace elemental patterns in the sands can be attributed to fractionation of dense minerals, including zircon, during the sedimentation process. The variations of Nd isotopes in conjunction with the petrographic parameters of lithic metamorphic (Lm) and volcanic (Lv) fragments allow a two-fold classification of the sands. These two sand types can be interpreted in terms of mixing among three different provenances: one volcanic rock-suit with less negative ε Nd (O) parameter than the other volcanic suite, and a third metasedimentary source with ε Nd (O) value of around -12, which is considered to be similar to the average western Brazilian shield composition. Thus the overall compositions of the sands has been modeled as mechanical mixtures of two components, an Andean magmatic arc and the Brazilian shield-derived metasediments. The model is strongly supported by a plot of ε Nd (O) versus ε Sr (O) of the sands. In this plot, the Type 1 and 2 sands define two coherent hyperbolic trends contiguous with two different portions of the Andean magmatic trend. (orig./WB)

  6. 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.

  7. Isotope geochemistry and fluxes of carbon and organic matter in tropical small mountainous river systems and adjacent coastal waters of the Caribbean

    Science.gov (United States)

    Moyer, Ryan; Bauer, James; Grottoli, Andrea

    2012-01-01

    Recent studies have shown that small mountainous rivers (SMRs) may act as sources of aged and/or refractory carbon (C) to the coastal ocean, which may increase organic C burial at sea and subsidize coastal food webs and heterotrophy. However, the characteristics and spatial and temporal variability of C and organic matter (OM) exported from tropical SMR systems remain poorly constrained. To address this, the abundance and isotopic character (δ13C and Δ14C) of the three major C pools were measured in two Puerto Rico SMRs with catchments dominated by different land uses (agricultural vs. non-agricultural recovering forest). The abundance and character of C pools in associated estuaries and adjacent coastal waters were also examined. Riverine dissolved and particulate organic C (DOC and POC, respectively) concentrations were highly variable with respect to land use and sampling month, while dissolved inorganic C (DIC) was significantly higher at all times in the agricultural catchment. In both systems, riverine DOC and POC ranged from modern to highly aged (2,340 years before present), while DIC was always modern. The agricultural river and irrigation canals contained very old DOC (1,184 and 2,340 years before present, respectively), which is consistent with findings in temperate SMRs and indicates that these tropical SMRs provide a source of aged DOC to the ocean. During months of high river discharge, OM in estuarine and coastal waters had C isotope signatures reflective of direct terrestrial input, indicating that relatively unaltered OM is transported to the coastal ocean at these times. This is also consistent with findings in temperate SMRs and indicates that C transported to the coastal ocean by SMRs may differ from that of larger rivers because it is exported from smaller catchments that have steeper terrains and fewer land-use types.

  8. The 8th ICGG International Conference on Gas Geochemistry Preface: Fluids and tectonics

    Directory of Open Access Journals (Sweden)

    F. Italiano

    2007-06-01

    Full Text Available The 8th International Conference on Gas Geochemistry provided the opportunity for scientists from different countries to meet each other, exchange ideas on the state of the art in gas geochemistry, and discuss advance in fluid geochemistry. The 8th ICGG meeting focused on three main geologic environments currently interacting with the human life: volcanoes, earthquakes and hydrocarbons. Ninety-four presentations gave participants chance to cover a variety of important research topics on gas geochemistry in geosciences including: gas migration in terrestrial and marine environments, Earth degassing and its relation to seismicity, volcanic eruptions, rare gases and application of isotope techniques, measurement and analytical techniques.

  9. High spatial resolution U-Pb geochronology and Pb isotope geochemistry of magnetite-apatite ore from the Pea Ridge iron oxide-apatite deposit, St. Francois Mountains, southeast Missouri, USA

    Science.gov (United States)

    Neymark, Leonid; Holm-Denoma, Christopher S.; Pietruszka, Aaron; Aleinikoff, John N.; Fanning, C. Mark; Pillers, Renee M.; Moscati, Richard J.

    2016-01-01

    The Pea Ridge iron oxide-apatite (IOA) deposit is one of the major rhyolite-hosted magnetite deposits of the St. Francois Mountains terrane, which is located within the Mesoproterozoic (1.5–1.3 Ga) Granite-Rhyolite province in the U.S. Midcontinent. Precise and accurate determination of the timing and duration of oreforming processes in this deposit is crucial for understanding its origin and placing it within a deposit-scale and regional geologic context. Apatite and monazite, well-established U-Pb mineral geochronometers, are abundant in the Pea Ridge orebody. However, the potential presence of multiple generations of dateable minerals, processes of dissolution-reprecipitation, and occurrence of micrometer-sized intergrowths and inclusions complicate measurements and interpretations of the geochronological results. Here, we employ a combination of several techniques, including ID-TIMS and high spatial resolution geochronology of apatite and monazite using LA-SC-ICPMS and SHRIMP, and Pb isotope geochemistry of pyrite and magnetite to obtain the first direct age constraints on the formation and alteration history of the Pea Ridge IOA deposit. The oldest apatite TIMS 207Pb*/206Pb* dates are 1471 ± 1 and 1468 ± 1 Ma, slightly younger than (but within error of) the ~1474 to ~1473 Ma U-Pb zircon ages of the host rhyolites. Dating of apatite and monazite inclusions within apatite provides evidence for at least one younger metasomatic event at ~1.44 Ga, and possibly multiple superimposed metasomatic events between 1.47 and 1.44 Ga. Lead isotop analyses of pyrite show extremely radiogenic 206Pb/204Pb ratios up to ~80 unsupported by in situ U decay. This excess radiogenic Pb in pyrite may have been derived from the spatially associated apatite as apatite recrystallized several tens of million years after its formation. The low initial 206Pb/204Pb ratio of ~16.5 and 207Pb/204Pb ratio of ~15.4 for individual magnetite grains indicate closed U-Pb system behavior in

  10. Strontium-90 and promethium-147 recovery

    International Nuclear Information System (INIS)

    Hoisington, J.E.; McDonell, W.R.

    1982-01-01

    Strontium-90 and promethium-147 are fission product radionuclides with potential for use as heat source materials in high reliability, non-interruptible power supplies. Interest has recently been expressed in their utilization for Department of Defense (DOD) applications. This memorandum summarizes the current inventories, the annual production rates, and the possible recovery of Sr-90 and Pm-147 from nuclear materials production operations at Hanford and Savannah River. Recovery of these isotopes from LWR spend fuel utilizing the Barnwell Nuclear Fuels Plant (BNFP) is also considered. Unit recovery costs at each site are provided

  11. Thermoluminescence of strontium tetraborate

    International Nuclear Information System (INIS)

    Santiago, M.; Caselli, E.; Lester, M.

    1999-01-01

    The thermoluminescent properties of crystalline strontium tetraborate are reported. Without activators it has an efficiency comparable to that of TLD-700 powder. Its fading after 40 days amount to less than 2%. The isometric plot shows that most of the emitted light is concentrated at wavelengths ranging from 350 to 450 nm, which accounts partially for the high efficiency. (author)

  12. Cryogenian alkaline magmatism in the Southern Granulite Terrane, India: Petrology, geochemistry, zircon U-Pb ages and Lu-Hf isotopes

    Science.gov (United States)

    Santosh, M.; Yang, Qiong-Yan; Ram Mohan, M.; Tsunogae, T.; Shaji, E.; Satyanarayanan, M.

    2014-11-01

    22 Ma correlating with the ages of the basement rocks from these areas. The initial 176Hf/177Hf isotope ratios of the zircon grains from the AM syenite fall in the range between 0.281771 and 0.282284, with moderately negative εHf(t) values between - 5.9 and 0.1. Similarly, the initial 176Hf/177Hf isotope ratios for the zircon grains of PM ultrapotassic granite range between 0.281197 and 0.281970, albeit with more negative εHf(t) values in the range between - 22.7 and - 0.3 (average εHf (t) value - 18.8). The Lu-Hf data suggest the involvement of variable extent of older crust with distinct crustal residence times, either in the form of assimilation during magma emplacement, or crustal recycling during magma genesis. Based on the geochemical and isotopic systematics, a possible petrogenetic model would be asthenospheric upwelling in an extensional setting, melting of enriched lithosphere, and interaction of the magmas with lower crustal domains with subduction-related components of various ages. The disposition of these alkali plutons along two paleo sutures that weld the Meso-Neoarchean crustal blocks in the northern periphery of SGT suggests that the zones of emplacement might represent an aborted rift. The paleo-sutures probably served as a weak zone along which extension occurred broadly coeval with the Cryogenian subduction further south.

  13. U–Pb, Rb–Sr, and U-series isotope geochemistry of rocks and fracture minerals from the Chalk River Laboratories site, Grenville Province, Ontario, Canada

    International Nuclear Information System (INIS)

    Neymark, L.A.; Peterman, Z.E.; Moscati, R.J.; Thivierge, R.H.

    2013-01-01

    Highlights: • AECL evaluates Chalk River Laboratories site as potential nuclear waste repository. • Isotope-geochemical data for rocks and fracture minerals at CRL site are reported. • Zircons from gneiss and granite yielded U–Pb ages of 1472 ± 14 and 1045 ± 6 Ma. • WR Rb–Sr and Pb–Pb systems do not show substantial large-scale isotopic mobility. • U-series and REE data do not support oxidizing conditions at depth in the past 1 Ma. - Abstract: As part of the Geologic Waste Management Facility feasibility study, Atomic Energy of Canada Ltd. (AECL) is evaluating the suitability of the Chalk River Laboratories (CRL) site in Ontario, situated in crystalline rock of the southwestern Grenville Province, for the possible development of an underground repository for low- and intermediate-level nuclear waste. This paper presents petrographic and trace element analyses, U–Pb zircon dating results, and Rb–Sr, U–Pb and U-series isotopic analyses of gneissic drill core samples from the deep CRG-series characterization boreholes at the CRL site. The main rock types intersected in the boreholes include hornblende–biotite (±pyroxene) gneisses of granitic to granodioritic composition, leucocratic granitic gneisses with sparse mafic minerals, and garnet-bearing gneisses with variable amounts of biotite and/or hornblende. The trace element data for whole-rock samples plot in the fields of within-plate, syn-collision, and volcanic arc-type granites in discrimination diagrams used for the tectonic interpretation of granitic rocks. Zircons separated from biotite gneiss and metagranite samples yielded SHRIMP-RG U–Pb ages of 1472 ± 14 (2σ) and 1045 ± 6 Ma, respectively, in very good agreement with widespread Early Mesoproterozoic plutonic ages and Ottawan orogeny ages in the Central Gneiss Belt. The Rb–Sr, U–Pb, and Pb–Pb whole-rock errorchron apparent ages of most of the CRL gneiss samples are consistent with zircon U–Pb age and do not indicate

  14. The Cambrian to Devonian odyssey of the Brabant Massif within Avalonia: A review with new zircon ages, geochemistry, Sm-Nd isotopes, stratigraphy and palaeogeography

    Science.gov (United States)

    Linnemann, Ulf; Herbosch, Alain; Liégeois, Jean-Paul; Pin, Christian; Gärtner, Andreas; Hofmann, Mandy

    2012-05-01

    This study provides an up-to-date and comprehensive review of the Early Palaeozoic evolution of the Brabant Massif belonging to the Anglo-Brabant Deformation Belt. Situated at the southeastern side of Avalonia microplate, it is the only well-known part of the northern passive margin of the Rheic Ocean. The Cambrian-Silurian sedimentary pile is > 13 km thick, with > 9 km for the Cambrian only. The unraveling of this continuous registration reflects the successive rifting and drifting of Avalonia from the Gondwana mainland, followed by soft-collisional processes with Baltica and finally the formation of Laurussia. Based on recently established detailed stratigraphy, sedimentology and basin development, on U-Pb LA-ICP-MS analyses of igneous and detrital zircon grains along with geochemical data including Sm-Nd isotopes, a new geodynamic and palaeogeographic evolution is proposed. Brabant Megasequence 1 (lower Cambrian to lowermost Ordovician, > 9 km thick) represents an embayment of the peri-Gondwanan rift from which the Rheic Ocean has evolved. Detrital zircon ages demonstrate that the Brabant is a typical peri-Gondwanan terrane with a major Pan-African (Neoproterozoic age) and a mixed West African and Amazonian source (Palaeoproterozoic, Archaean and some Mesoproterozoic age). The transition towards the Avalonia drifting is marked by an unconformity and a short volcanic episode. The northward drift of Avalonia towards Baltica is recorded by the Megasequence 2 (Middle to Upper Ordovician, 1.3 km thick). The source for Mesoproterozoic zircons vanished, as the result of the Rheic Ocean opening and the isolation from Amazonian sources. The transition to Megasequence 3 is marked by a drastic change in palaeobathymetry and an important (sub)volcanic episode during a tectonic instability period (460-430 Ma), reflecting the Avalonia-Baltica soft docking as also shown by the reappearance of Mesoproterozoic detrital zircons, typical of Baltica. Unradiogenic Nd isotope

  15. Stable Isotope Geochemistry of Extremely Well-Preserved 2.45-Billion-Year-Old Hydrothermal Systems in the Vetreny Belt, Baltic Shield: Insights into Paleohydrosphere

    Science.gov (United States)

    Zakharov, D. O.; Bindeman, I. N.

    2015-12-01

    The early Paleoproterozoic was an eventful period in the Earth's history. The first portions of free oxygen emerged in the atmosphere, Snowball Earth glaciations happened several times and the first supercontinent broke up due to extensive rifting. These events should have affected the stable isotopic composition of the hydrosphere. In this study, we use rocks that were altered in underwater hydrothermal systems to investigate the stable isotopic composition of the hydrosphere 2.39-2.45 billion years ago (hereinafter, Ga). Extremely low-δ18O (down to -27.5‰ SMOW) rocks from 2.39 Ga metamorphosed subglacial hydrothermal systems of the Belomorian belt, Baltic Shield formed at near-equatorial latitudes suggesting a Snowball (or Slushball) Earth glaciation. These results motivated us to look at temporally and geographically close hydrothermal systems from the unmetamorhposed 2.45 Ga Vetreny Belt rift. The length of the rift is 250 km and it is composed of high-Mg basalts, mafic-ultramafic intrusions and sedimentary successions. We examined several localities of high-Mg basalt flows that include astonishingly fresh pillow lavas, often with preserved volcanic glass, eruptive breccias, and hydrothermal alteration zones. Collected samples serve a great textural evidence of water-rock interaction that occurred in situ while basalts were cooling. The preliminary results from coexisting quartz and epidote (T, D18O=311°C), and from coexisting calcite and quartz (T, D18O=190°C) yield values of δ18O of involved water between -1.6 and -0.9 ‰. The values of δ13C in calcites vary between -4.0 and -2.3 ‰. It is likely that hydrothermal fluids operated in the Vetreny Belt rift were derived from seawater that is no different from modern oceanic water in terms of δ18O. Apparently, the rift was a Paleoproterozoic analog of the modern Red Sea, filled with oceanic water. The result is important because the Vetreny Belt rift predates the onset of Snowball Earth glaciation at 2

  16. Micromorphology and stable-isotope geochemistry of historical pedogenic siderite formed in PAH-contaminated alluvial clay soils, Tennessee, U.S.A

    Science.gov (United States)

    Driese, S.G.; Ludvigson, Greg A.; Roberts, J.A.; Fowle, D.A.; Gonzalez, Luis A.; Smith, J.J.; Vulava, V.M.; McKay, L.D.

    2010-01-01

    Alluvial clay soil samples from six boreholes advanced to depths of 400-450 cm (top of limestone bedrock) from the Chattanooga Coke Plant (CCP) site were examined micromorphologically and geochemically in order to determine if pedogenic siderite (FeCO3) was present and whether siderite occurrence was related to organic contaminant distribution. Samples from shallow depths were generally more heavily contaminated with polycyclic aromatic hydrocarbons (PAHs) than those at greater depth. The upper 1 m in most boreholes consisted of mixtures of anthropogenically remolded clay soil fill containing coal clinker, cinder grains, and limestone gravel; most layers of coarse fill were impregnated with creosote and coal tar. Most undisturbed soil (below 1 m depth) consisted of highly structured clays exhibiting fine subangular blocky ped structures, as well as redox-related features. Pedogenic siderite was abundant in the upper 2 m of most cores and in demonstrably historical (< 100 years old) soil matrices. Two morphologies were identified: (1) sphaerosiderite crystal spherulites ranging from 10 to 200 um in diameter, and (2) coccoid siderite comprising grape-like "clusters" of crystals 5-20 ??n in diameter. The siderite, formed in both macropores and within fine-grained clay matrices, indicates development of localized anaerobic, low-Eh conditions, possibly due to microbial degradation of organic contaminants. Stable-isotope compositions of the siderite have ??13C values spanning over 25%o (+7 to - 18%o VPDB) indicating fractionation of DIC by multiple microbial metabolic pathways, but with relatively constant ??18O values from (-4.8 ?? 0.66%o VPDB) defining a meteoric sphaerosiderite line (MSL). Calculated isotope equilibrium water ??18O values from pedogenic siderites at the CCP site are from 1 to 5 per mil lighter than the groundwater ??18O values that we estimate for the site. If confirmed by field studies in progress, this observation might call for a reevaluation of

  17. Investigating the hydrological significance of stalagmite geochemistry (Mg, Sr) using Sr isotope and particulate element records across the Late Glacial-to-Holocene transition

    Science.gov (United States)

    Belli, R.; Borsato, A.; Frisia, S.; Drysdale, R.; Maas, R.; Greig, A.

    2017-02-01

    The trace element and Sr isotope records in two coeval stalagmites characterized by different growth rates and flow regimes at Savi cave (Grotta Savi, NE Italy) reveal different sources and incorporation mechanisms for Mg and Sr. Mg is sourced primarily from dissolved cave host rock while particulate Mg derived from soil plays a subordinate role. The presence of particulate-borne Mg is inferred from the co-variation of Mg and particle-associated elements (Th, Al and Mn) which are preferentially concentrated in open columnar calcite layers. Variation in Mg concentrations corrected for particle-influenced components, the Mgc parameter, is controlled by water-rock interaction, with higher and lower Mgc during dry and wet phases, respectively. This is thought to reflect incongruent dissolution of Mg-rich phases. Correction of Sr concentrations for contributions from airborne exogenic Sr, based on 87Sr/86Sr ratios, yields the bedrock-only contribution (Src). Src variation in stalagmite calcite is influenced by speleothem growth rate and by variation of the calcite-water Sr partitioning in wet and dry phases, and only to a minor extent by incongruent dissolution of Mg-rich phases. Concentration profiles for Mgc and Srcg (corrected for growth rate effects) show inverse correlations and are inferred to show hydrological significance which is captured in a hydrological index, HI. We suggest HI provides robust information on water-rock interaction related to hydrological changes and can be utilized in both wet and semi-arid environments, provided the corrections for soil Mg and exogenic Sr can be applied with confidence. Application of the HI index allows correction of Grotta Savi oxygen isotope data, to yield a δ18Oc time series that shows when changes in moisture sources and atmospheric reorganization, or changes in moisture amount, were significant. This is especially evident during the Younger Dryas (YD). The Savi record supports the concept of a two-phase YD, marked by

  18. Noble Gas geochemistry of the newly discovered hydrothermal fields in the Gulf of California: preliminary He-isotope ratios from the Alarcon Rise and Pescadero basin vent sites

    Science.gov (United States)

    Spelz, R. M.; Lupton, J. E.; Evans, L. J.; Zierenberg, R. A.; Clague, D. A.; Neumann, F.; Paduan, J. B.

    2015-12-01

    Numerous submarine deep-sea hydrothermal vents related to volcanic activity of the East Pacific Rise (EPR) are situated along the Pacific margins of Mexico. Until recently, active hydrothermal venting was unknown between the Guaymas Basin and 21°N on the EPR. MBARI's recent oceanographic surveys have added 7 new active vent sites. In this study, we aimed to sample the high-temperature hydrothermal fluids emanating from two distinct vent sites, named Meyibo and Auka, located in the Alarcon Rise and Pescadero Basin, respectively. Mantle-derived He have long been identified in hydrothermal fluid releases. The presence of He in aqueous fluids with 3He/4He ratios greater than in-situ production values (~0.05 RA, where RA = air He or 1.4 x 10-6) indicates the presence of mantle-derived melts. Preliminary analyses of He-isotope ratios derived from the newly discovered Meyibo and Auka hydrothermal fields show high 3He/4He ratios (~8RA), typical of MORB's. Auka vent field, characterized by chimneys composed of light carbonate minerals and oil-like hydrocarbons, and temperatures between 250-290oC, show average values of ~7.87RA. In contrast, the black-smokers at the Meyibo field, composed of dark sulfide minerals and temperatures over 350oC, yielded a higher He ratio of ~8.24RA. Recently, it has become clear that regional maximum mantle He values correlate with the velocity structure in the mantle, therefore, He has the potential to map regions of the underlying mantle that are undergoing partial melting. Seismic records could then be compared with the geochemical He ratio signal and supply information regarding tectonics and other processes involved in the generation of these gases. The data presented here will be completing a totally new inventory of He results from hydrothermal vents in the EPR and fault-termination basins distributed along the P-NA plate boundary in the Gulf of California. The results will be further coupled with the analysis of other geochemical

  19. Baseline Geochemistry of Natural Occurring Methane and Saline Groundwater in an Area of Unconventional Shale Gas Development Through Time

    Science.gov (United States)

    Harkness, J.; Darrah, T.; Warner, N. R.; Whyte, C. J.; Moore, M. T.; Millot, R.; Kloppmann, W.; Jackson, R. B.; Vengosh, A.

    2017-12-01

    Naturally occurring methane is nearly ubiquitous in most sedimentary basins and delineating the effects of anthropogenic contamination sources from geogenic sources is a major challenge for evaluating the impact of unconventional shale gas development on water quality. This study employs a broadly integrated study of various geochemical techniques to investigate the geochemical variations of groundwater and surface water before, during, and after hydraulic fracturing.This approache combines inorganic geochemistry (major cations and anions), stable isotopes of select inorganic constituents including strontium (87Sr/86Sr), boron (δ11B), lithium (δ7Li), and carbon (δ13C-DIC), select hydrocarbon molecular (methane, ethane, propane, butane, and pentane) and isotopic tracers (δ13C-CH4, δ13C-C2H6), tritium (3H), and noble gas elemental and isotopic composition (He, Ne, Ar) to apportion natural and anthropogenic sources of natural gas and salt contaminants both before and after drilling. Methane above 1 ccSTP/L in groundwater samples awas strongly associated with elevated salinity (chloride >50 mg/L).The geochemical and isotopic analysis indicate saline groundwater originated via naturally occurring processes, presumably from the migration of deeper methane-rich brines that have interacted extensively with coal lithologies. The chemistry and gas compostion of both saline and fresh groundwater wells did not change following the installation of nearby shale-gas wells.The results of this study emphasize the value of baseline characterization of water quality in areas of fossil fuel exploration. Overall this study presents a comprehensive geochemical framework that can be used as a template for assessing the sources of elevated hydrocarbons and salts to water resources in areas potentially impacted by oil and gas development.

  20. Devonian alkaline magmatism in the northern North China Craton: Geochemistry, SHRIMP zircon U-Pb geochronology and Sr-Nd-Hf isotopes

    Directory of Open Access Journals (Sweden)

    Dingling Huang

    2017-01-01

    Full Text Available The Wulanhada pluton is among the rare suite of Devonian alkaline plutons occurring along the northern margin of the North China Craton (NCC. The intrusion is mainly composed of quartz-monzonite. Here we report zircon SHRIMP U-Pb data from this intrusion which shows emplacement age of ca. 381.5 Ma. The rock is metaluminous with high (Na2O + K2O values ranging from 8.46 to 9.66 wt.%. The REE patterns of the rocks do not show any Eu anomaly whereas the primitive-mantle-normalized spider diagram shows strong positive Sr and Ba anomalies. The Wulanhada rocks exhibit high initial values of (87Sr/86Srt = 0.70762–0.70809, low ɛNd(t = −12.76 to −12.15 values and negative values of ɛHf(t = −23.49 to −17.02 with small variations in (176Hf/177Hft (0.281873–0.282049. These geochemical features and quantitative isotopic modeling results suggest that the rocks might have been formed through the partial melting of Neoarchean basic rocks in the lower crust of the NCC. The Wulanhada rocks, together with the Devonian alkaline rocks and mafic-ultramafic complex from neighboring regions, constitute a post-collisional magmatic belt along the northern NCC.

  1. Using biochemical and isotope geochemistry to understand the environmental and public health implications of lead pollution in the lower Guadiana River, Iberia: A freshwater bivalve study

    Energy Technology Data Exchange (ETDEWEB)

    Company, R. [CIMA, Faculty of Marine and Environmental Sciences, University of Algarve, Campus de Gambelas, 8005-139 Faro (Portugal)], E-mail: rcompany@ualg.pt; Serafim, A.; Lopes, B.; Cravo, A. [CIMA, Faculty of Marine and Environmental Sciences, University of Algarve, Campus de Gambelas, 8005-139 Faro (Portugal); Shepherd, T.J.; Pearson, G. [Department of Earth Sciences, Durham University, Science Labs., Durham DH1 3LE (United Kingdom); Bebianno, M.J. [CIMA, Faculty of Marine and Environmental Sciences, University of Algarve, Campus de Gambelas, 8005-139 Faro (Portugal)], E-mail: mbebian@ualg.pt

    2008-11-01

    Lead is a natural component of aquatic ecosystems with no known biological role and is highly toxic. Its toxicity stems from its ability to mimic biologically important metals and to produce membrane damage through lipid peroxidation (LPO). Most lead poisoning symptoms are thought to occur by interfering with an essential enzyme, {delta}-aminolevulinic acid dehydratase (ALAD), the activity of which is markedly inhibited by lead. The purpose of this work was to study the levels and effects of lead pollution (responses of ALAD and oxidative stress biomarker LPO) in the freshwater bivalve Corbicula fluminea along the lower Guadiana River (Portugal and Spain); a major river system impacted by historic mining pollution and more recent anthropogenic inputs. The results show that the enzymatic activity of ALAD is negatively correlated with the total Pb concentration of the whole tissue suggesting that ALAD has considerable potential as a biomarker of lead exposure in C. fluminea. To identify the sources of lead to which bivalves have been exposed, high precision {sup 206}Pb/{sup 204}Pb, {sup 207}Pb/{sup 204}Pb, {sup 208}Pb/{sup 204}/Pb ratios for C. fluminea confirm that historical mining activities in the Iberian Pyrite Belt are the dominant source of lead pollution in the lower Guadiana River. The isotope patterns however exhibit marked seasonal and geographic variation in response to rainfall and river water management. Locally, other anthropogenic sources of lead have been detected in C. fluminea close to population centres, thus adding to its versatility as a freshwater bio-indicator. Overall, the study highlights the value of natural ecosystems as monitors of water quality and their importance for public health assessment and surveillance.

  2. Hydro geochemistry and isotopic approach of coastal aquifer systems of Cap Bon : The case of tablecloths and the eastern coast of El Haourai - Tunisia

    International Nuclear Information System (INIS)

    Ben Hammouda, Fethi

    2008-01-01

    As many other semi-arid regions, the Cap Bon peninsula (N.E. Tunisia) shows a parallel increase in overexploitation and mineralization of groundwater resources. In the eastern coast and El Haouaria aquifers, the groundwater quality is threatened. Surveys including level measurements, water sampling, chemical analysis (ions Na+, Cl., Ca2+, Mg2+, Br.) and sotopes (18O, 2H, 3H, 13C, 14C) were performed in 2001, 2002 and 2003. Several analysis types were conducted and results are compared with the hydrodynamic information for identifying the main processes involved in the mineralization increase. Particularly, the isotopes were permitting the understanding of the hydrogeological of the concerned aquifers and the localization of the recharge zones. Because the regional situation along the seashore, the seawater intrusion in the unconfined Plio-quaternary aquifer, resulting from the groundwater overexploitation, and obvious explanation for the rising salinity is identified but is not the only cause of the qualitative degradation: the irrigation development that induces the soil leaching and the fertilizers transfer to groundwater over the whole aquifer extent is another major reason of the mineralization increase. Piezometric and salinity maps of the Plio-quaternary aquifer were established. The continuous increase in pumping has created several depressions in the water table, up to 12 m below msl and induced a deterioration of the water quality. The temporal changes in water-table level and salinity are often similar which suggests a strong link between them. Several geochemical approaches were performed to identify the importance of the marine intrusion in the increase in mineralization. The salinity of the groundwater appears to originate from dissolution of minerals in the aquifer system

  3. Constraints from geochemistry and oxygen isotopes for the hydrothermal origin of orthoamphibole mafic gneiss in the New Jersey Highlands, north-central Appalachians, USA

    Science.gov (United States)

    Volkert, Richard A.; Peck, William H.

    2017-12-01

    Rare exposures of orthoamphibole mafic (Oam) gneiss of Mesoproterozoic age in the north-central Appalachians are confined to the northwestern New Jersey Highlands where they form thin lens-shaped bodies composed of gedrite and sparse anthophyllite, oligoclase (An13-An20), biotite, magnetite, and local fluorapatite, rutile, and ilmenite. The gneiss is penetratively foliated and has sharp, conformable contacts against enclosing supracrustal paragneiss and marble. Orthoamphibole mafic gneiss is characterized by low SiO2 (48 ± 2.5 wt%), CaO (1.9 ± 1.3 wt%), and high Al2O3 (18 ± 1.2 wt%), Fe2O3 (10.5 ± 1.6 wt%), and MgO (12 ± 2.3 wt%). Trace element abundances overlap those of unaltered amphibolites in the study area and, coupled with δ18O values of 9.45 ± 0.6‰ (VSMOW) from gedrite separates, support an origin from a basalt protolith. The geochemical and isotopic data are consistent with the formation of Oam gneiss through sea floor hydrothermal alteration of basalt at low temperature of 150-200 °C. Mass-balance calculations indicate gains during alteration mainly in MgO and Al2O3 and losses in CaO, Sr, and light rare earth elements. Our results are compatible with the pre-metamorphic alteration of the basalt protoliths through chloritization and plagioclase dissolution that produced a Mg-rich and Ca-poor rock. Subsequent metamorphism of this chlorite-rich rock to the current mineral assemblage of Oam gneiss took place at ca. 1045 Ma, during the Ottawan phase of the Grenvillian Orogeny. The close spatial association in the study area of Oam gneiss bodies and sulfide occurrences suggests an affinity to the style of mineralization associated with volcanogenic massive sulfide (VMS)-type deposits.

  4. Using biochemical and isotope geochemistry to understand the environmental and public health implications of lead pollution in the lower Guadiana River, Iberia: a freshwater bivalve study.

    Science.gov (United States)

    Company, R; Serafim, A; Lopes, B; Cravo, A; Shepherd, T J; Pearson, G; Bebianno, M J

    2008-11-01

    Lead is a natural component of aquatic ecosystems with no known biological role and is highly toxic. Its toxicity stems from its ability to mimic biologically important metals and to produce membrane damage through lipid peroxidation (LPO). Most lead poisoning symptoms are thought to occur by interfering with an essential enzyme, delta-aminolevulinic acid dehydratase (ALAD), the activity of which is markedly inhibited by lead. The purpose of this work was to study the levels and effects of lead pollution (responses of ALAD and oxidative stress biomarker LPO) in the freshwater bivalve Corbicula fluminea along the lower Guadiana River (Portugal and Spain); a major river system impacted by historic mining pollution and more recent anthropogenic inputs. The results show that the enzymatic activity of ALAD is negatively correlated with the total Pb concentration of the whole tissue suggesting that ALAD has considerable potential as a biomarker of lead exposure in C. fluminea. To identify the sources of lead to which bivalves have been exposed, high precision (206)Pb/(204)Pb, (207)Pb/(204)Pb, (208)Pb/(204)/Pb ratios for C. fluminea confirm that historical mining activities in the Iberian Pyrite Belt are the dominant source of lead pollution in the lower Guadiana River. The isotope patterns however exhibit marked seasonal and geographic variation in response to rainfall and river water management. Locally, other anthropogenic sources of lead have been detected in C. fluminea close to population centres, thus adding to its versatility as a freshwater bio-indicator. Overall, the study highlights the value of natural ecosystems as monitors of water quality and their importance for public health assessment and surveillance.

  5. Using biochemical and isotope geochemistry to understand the environmental and public health implications of lead pollution in the lower Guadiana River, Iberia: A freshwater bivalve study

    International Nuclear Information System (INIS)

    Company, R.; Serafim, A.; Lopes, B.; Cravo, A.; Shepherd, T.J.; Pearson, G.; Bebianno, M.J.

    2008-01-01

    Lead is a natural component of aquatic ecosystems with no known biological role and is highly toxic. Its toxicity stems from its ability to mimic biologically important metals and to produce membrane damage through lipid peroxidation (LPO). Most lead poisoning symptoms are thought to occur by interfering with an essential enzyme, δ-aminolevulinic acid dehydratase (ALAD), the activity of which is markedly inhibited by lead. The purpose of this work was to study the levels and effects of lead pollution (responses of ALAD and oxidative stress biomarker LPO) in the freshwater bivalve Corbicula fluminea along the lower Guadiana River (Portugal and Spain); a major river system impacted by historic mining pollution and more recent anthropogenic inputs. The results show that the enzymatic activity of ALAD is negatively correlated with the total Pb concentration of the whole tissue suggesting that ALAD has considerable potential as a biomarker of lead exposure in C. fluminea. To identify the sources of lead to which bivalves have been exposed, high precision 206 Pb/ 204 Pb, 207 Pb/ 204 Pb, 208 Pb/ 204 /Pb ratios for C. fluminea confirm that historical mining activities in the Iberian Pyrite Belt are the dominant source of lead pollution in the lower Guadiana River. The isotope patterns however exhibit marked seasonal and geographic variation in response to rainfall and river water management. Locally, other anthropogenic sources of lead have been detected in C. fluminea close to population centres, thus adding to its versatility as a freshwater bio-indicator. Overall, the study highlights the value of natural ecosystems as monitors of water quality and their importance for public health assessment and surveillance

  6. Crustal evolution of South American Platform based on Sm-Nd isotope geochemistry; Evolucao crustal da plataforma sul americana com base na geoquimica isotopica Sm-Nd

    Energy Technology Data Exchange (ETDEWEB)

    Sato, Kei

    1998-07-01

    Sm-Nd isotopic systematics is relevant to the topics of origin and evolution the of continental crust, where model ages refer to the time when crustal material was differentiated from the upper mantle. Alternative interpretations are due to a lack of adequate information on crustal processes and the variable composition of the mantle sources. The Sm-Nd methods are presented, and applied on rock materials from the South American Platform. The main conclusions indicate juvenile accretion with higher growth rates (peaks), around 3.7-3.5 Ga ({approx} 0.5% in volume), 3.1 - 2.9 Ga ({approx}16%), 2.7 - 2.6 ({approx} 9%), 2.2 - 1.9 (35%) and 1.3-1.0 (7%). The continental growth curve indicates that about 35 % of the crust was formed by 2.5 Ga, 88% by 1.8 Ga and 99% by 1.0 Ga, and the remaining {approx} 1 % was added in the Phanerozoic. Rapid crustal growth occurred between 2.2 and 1.9 Ga. The main period of continental crust formation occurred during the Paleoproterozoic, corresponding to 54 % in volume. Sm-Nd model ages, when compared with the crystallisation ages of granitoid rocks, furnish a rough estimate of juvenile vs. reworked material. Within the South American Platform about 45% of juvenile continental crust is still preserved within tectonic provinces of different ages. The remainder represents continental crust reworked in younger tectono-thermal events. In particular crustal reworking was predominating over juvenile accretion during Meso-Neoproterozoic. The Transbrasiliano Lineament is a megasuture, active in the Neoproterozoic, which separates a large northwestern mass, including the Amazonian and Sao Luis Cratons, from a southeastern mass, formed by a collage of cratonic fragments, of which the Sao Francisco and Rio de La Plata are the largest. The crustal evolutions of these two large continental masses are considered individually, and can be resumed following form: I - Old Archean rocks (>3.4 Ga) are found only within the south-eastern part (Gaviao Block

  7. Geochemistry and Petrogenesis of Biabanak–Bafq Mafic Mgmatism ...

    Indian Academy of Sciences (India)

    59

    13185-1494. Email: m_poshtkoohi@yahoo.com; Mobile No: +98 912 209 39 73 ...... petrologie et tectonique du precambrien et de sa couverture, Ph.D. thesis, universite ..... Applications of the 190Pt–186OS isotope system to geochemistry and.

  8. Zircon U-Pb age, Lu-Hf isotope, mineral chemistry and geochemistry of Sundamalai peralkaline pluton from the Salem Block, southern India: Implications for Cryogenian adakite-like magmatism in an aborted-rift

    Science.gov (United States)

    Renjith, M. L.; Santosh, M.; Li, Tang; Satyanarayanan, M.; Korakoppa, M. M.; Tsunogae, T.; Subba Rao, D. V.; Kesav Krishna, A.; Nirmal Charan, S.

    2016-01-01

    The Sundamalai peralkaline pluton is one among the Cryogenian alkaline plutons occurring in the Dharmapuri Rift Zone (DRZ) of the Salem Block in the Southern Granulite Terrane (SGT) of India. Here we present zircon U-Pb age and Lu-Hf isotopic composition, mineral chemistry and geochemistry of the pluton to explore the petrogenesis and geodynamic implications. Systematic modal variation of orthoclase, Na-plagioclase, Ca-amphibole (ferro-edenite and hastingsite) and quartz developed quartz-monzonite and granite litho units in the Sundamalai pluton. Thermometry based on amphibole-plagioclase pair suggests that the pluton was emplaced and solidified at around 4.6 kbar pressure with crystallization of the major phases between 748 and 661 °C. Estimated saturation temperature of zircon (712-698 °C) is also well within this range. However, apatite saturation occurred at higher temperatures between 835 and 870 °C, in contrast with monazite saturation (718-613 °C) that continued up to the late stage of crystallization. Estimated oxygen fugacity values (log fO2: -14 to -17) indicate high oxidation state for the magma that stabilized titanite and magnetite. The magmatic zircons from Sundamalai pluton yielded a weighted mean 206Pb/238U age of 832.6 ± 3.2 Ma. Geochemically, the Sundamalai rocks are high-K to shoshonitic, persodic (Na2O/K2O ratio > 1), silica-saturated (SiO2:65-72 wt.%), and peralkaline in composition (aluminum saturation index, ASI Sc(2-3 ppm), positive Sr anomaly and predominantly negative zircon εHf(t) values (-10.8 to -9.3 with an average of -10.2) and initial 176Hf/177Hf ratios (0.281947-0.282022) confirm a Paleoproterozoic crustal source. Based on the field and geochemical evidences, we propose that a previously metasomatized mafic lower-crustal source enriched in alkalis has undergone CO2-present partial melting as a result of asthenospheric upwelling beneath an aborted rifting along the DRZ generating the magma that crystallized the Sundamalai rocks

  9. Analysis of radioactive strontium

    International Nuclear Information System (INIS)

    1977-01-01

    In environmental radiation survey, radioactive strontium has been analyzed in compliance with the manual ''Analyzing methods for radioactive strontium'' published in 1960 by the Science and Technology Agency, Japan, and revised in 1963. However, in a past decade, progress and development in analyzing methods and measuring equipments have been significant, therefore the manual was revised in 1974. Major revisions are as follows. (1) Analysis of 90 Sr with long half life was changed to the main theme and that of 89 Sr with short half life became a subordinate one. (2) Measuring criteria and sampling volume were revised. (3) Sample collection method was unified. (4) Analyzing method for soil was improved to NaOH-HCl method which has good recovery rate. (5) 90 Y separation method of simple operation was added for sea water analysis besides EDTA and fuming nitric acid methods. (6) Flame spectrometry for quantitative analysis of stable strontium was revised to atomic absorption spectrometry. The contents of the manual comprises 11 chapters describing introduction, measuring criteria for 90 Sr ( 89 Sr), rain and dust, land water, sea water, soil, sea bottom and river bottom sediments (changed from human urine and human bones), crops, milk (the previous one chapter was divided into two), marine organisms, and everyday foods, respectively. (Wakatsuki, Y.)

  10. Isotopes in day to day life

    Science.gov (United States)

    1984-06-01

    Developments are reported in the use of isotopic labeling and isotope irradiation in agriculture, medical science, hydrology, geochemistry, geophysics, environment pollution detection, and industries. Radioisotope instruments are described as well as techniques for gamma radiography, neutron radiography, and autoradiography. Isotope dating in geology and archaeology is covered. Basic scientific research topics in various areas are listed.

  11. DOE workshop: Sedimentary systems, aqueous and organic geochemistry

    International Nuclear Information System (INIS)

    1993-07-01

    A DOE workshop on sedimentary systems, aqueous and organic geochemistry was held July 15-16, 1993 at Lawrence Berkeley Laboratory. Papers were organized into several sections: Fundamental Properties, containing papers on the thermodynamics of brines, minerals and aqueous electrolyte solutions; Geochemical Transport, covering 3-D imaging of drill core samples, hydrothermal geochemistry, chemical interactions in hydrocarbon reservoirs, fluid flow model application, among others; Rock-Water Interactions, with presentations on stable isotope systematics of fluid/rock interaction, fluid flow and petotectonic evolution, grain boundary transport, sulfur incorporation, tracers in geologic reservoirs, geothermal controls on oil-reservoir evolution, and mineral hydrolysis kinetics; Organic Geochemistry covered new methods for constraining time of hydrocarbon migration, kinetic models of petroleum formation, mudstones in burial diagenesis, compound-specific carbon isotope analysis of petroleums, stability of natural gas, sulfur in sedimentary organic matter, organic geochemistry of deep ocean sediments, direct speciation of metal by optical spectroscopies; and lastly, Sedimentary Systems, covering sequence stratigraphy, seismic reflectors and diagenetic changes in carbonates, geochemistry and origin of regional dolomites, and evidence of large comet or asteroid impacts at extinction boundaries

  12. DOE workshop: Sedimentary systems, aqueous and organic geochemistry

    Energy Technology Data Exchange (ETDEWEB)

    1993-07-01

    A DOE workshop on sedimentary systems, aqueous and organic geochemistry was held July 15-16, 1993 at Lawrence Berkeley Laboratory. Papers were organized into several sections: Fundamental Properties, containing papers on the thermodynamics of brines, minerals and aqueous electrolyte solutions; Geochemical Transport, covering 3-D imaging of drill core samples, hydrothermal geochemistry, chemical interactions in hydrocarbon reservoirs, fluid flow model application, among others; Rock-Water Interactions, with presentations on stable isotope systematics of fluid/rock interaction, fluid flow and petotectonic evolution, grain boundary transport, sulfur incorporation, tracers in geologic reservoirs, geothermal controls on oil-reservoir evolution, and mineral hydrolysis kinetics; Organic Geochemistry covered new methods for constraining time of hydrocarbon migration, kinetic models of petroleum formation, mudstones in burial diagenesis, compound-specific carbon isotope analysis of petroleums, stability of natural gas, sulfur in sedimentary organic matter, organic geochemistry of deep ocean sediments, direct speciation of metal by optical spectroscopies; and lastly, Sedimentary Systems, covering sequence stratigraphy, seismic reflectors and diagenetic changes in carbonates, geochemistry and origin of regional dolomites, and evidence of large comet or asteroid impacts at extinction boundaries.

  13. Isotopes in everyday life

    International Nuclear Information System (INIS)

    Seligman, H.; Gillen, V.A.

    1990-12-01

    Isotopes represent a tool which can do certain jobs better, easier, quicker, more simply and cheaper than competitive methods. Some measurements could not be done at all without the use of isotopes as there are no alternative methods available. A short review of these tools of science in their different fields is given: food and agriculture, human health applications, industry, hydrology, geology, geochemistry, geophysics and dating, environment, basic scientific research

  14. Determination of strontium isotopic composition in natural waters: examples of application in subsurface waters of the coastal zone of Bragantina region, Para, BR; Determinacao da composicao isotopica de estroncio em aguas naturais: exemplos de sua aplicacao em aguas subsuperficiais da zona costeira na regiao Bragantina-PA

    Energy Technology Data Exchange (ETDEWEB)

    Bordalo, Adriana Oliveira; Moura, Candido Augusto Veloso; Scheller, Thomas [Universidade Federal do Para (UFPA), Belem, PA (Brazil). Centro de Geociencias]. E-mail: adriana@ufpa.br

    2007-07-15

    Analytical procedures used for determining the concentrations and isotope composition of strontium in subsurface waters, by mass spectrometry, are described. Sampling was performed in coastal plateaus, salt marsh and mangrove environments in the coastal region of Para. Coastal plateau waters have {delta}{sup 87}Sr between 1.51 and 6.26 per mille and Sr concentration bellow 58 ppb. Salt marsh waters show {delta}{sup 87}Sr between 0.55 and 0.90 per mille and Sr concentration between 93 and 114 ppm, while mangrove waters have {delta}{sup 87}Sr per mille around zero and Sr concentration above 15 ppm. Differences in the {sup 87}Sr/{sup 86}Sr ratio in these subsurface waters are detected, as well as seasonal variations in the coastal plateau waters. (author)

  15. Stable-isotope geochemistry of the Pierina high-sulfidation Au-Ag deposit, Peru: Influence of hydrodynamics on SO42--H2S sulfur isotopic exchange in magmatic-steam and steam-heated environments

    Science.gov (United States)

    Fifarek, R.H.; Rye, R.O.

    2005-01-01

    The Pierina high-sulfidation Au-Ag deposit formed 14.5 my ago in rhyolite ash flow tuffs that overlie porphyritic andesite and dacite lavas and are adjacent to a crosscutting and interfingering dacite flow dome complex. The distribution of alteration zones indicates that fluid flow in the lavas was largely confined to structures but was dispersed laterally in the tuffs because of a high primary and alteration-induced permeability. The lithologically controlled hydrodynamics created unusual fluid, temperature, and pH conditions that led to complete SO42--H2S isotopic equilibration during the formation of some magmatic-steam and steam-heated alunite, a phenomenon not previously recognized in similar deposits. Isotopic data for early magmatic hydrothermal and main-stage alunite (??34S=8.5??? to 31.7???; ??18 OSO4=4.9??? to 16.5???; ??18 OOH=2.2??? to 14.4???; ??D=-97??? to -39???), sulfides (??34 S=-3.0??? to 4.3???), sulfur (??34S=-1.0??? to 1.1???), and clay minerals (??18O=4.3??? to 12.5???; ??D=-126??? to -81???) are typical of high-sulfidation epithermal deposits. The data imply the following genetic elements for Pierina alteration-mineralization: (1) fluid and vapor exsolution from an I-type magma, (2) wallrock buffering and cooling of slowing rising vapors to generate a reduced (H2S/SO4???6) highly acidic condensate that mixed with meteoric water but retained a magmatic ??34S???S signature of ???1???, (3) SO2 disproportionation to HSO4- and H2S between 320 and 180 ??C, and (4) progressive neutralization of laterally migrating acid fluids to form a vuggy quartz???alunite-quartz??clay???intermediate argillic???propylitic alteration zoning. Magmatic-steam alunite has higher ??34S (8.5??? to 23.2???) and generally lower ??18OSO4 (1.0 to 11.5???), ??18OOH (-3.4 to 5.9???), and ??D (-93 to -77???) values than predicted on the basis of data from similar occurrences. These data and supporting fluid-inclusion gas chemistry imply that the rate of vapor ascent for this

  16. Geochemistry and ore prospecting

    International Nuclear Information System (INIS)

    Le Caignec, R.

    1954-01-01

    Applied geochemistry is a new technique which helps the geologist in detecting ore deposits. Some deposits, even when they are covered with rather thick surface structures, form around these zones where the infinitesimal content of some elements of soils or waters is notably different. These 'anomalies' may be contemporaneous to the deposit-structure (primary dispersion) or may have occurred later (secondary dispersion). Various factors rule these anomalies: ore-stability, soil homogeneity, water conditions, topography, vegetation, etc... Applied geochemistry is in fact the study of analysis techniques of metal traces in soils as well as the geological interpretation of observed anomalies. This report gives practical data on sampling methods, yields, costs and also on special problems of uranium geochemistry. (author) [fr

  17. Proceedings of the 3. International symposium environmental geochemistry in tropical countries. Book of abstracts

    International Nuclear Information System (INIS)

    1999-01-01

    Theoretical and experimental papers are presented in these proceedings covering the following subjects: uranium mining and milling, geochemistry, land and water pollution, mineral wastes, iodine isotopes, gas chromatography, separation processes, environmental quality, qualitative and quantitative chemical analysis, rare earths, uranium isotopes, ground water, radionuclide migration, and sedimentary basins

  18. Using geochemistry to identify the source of groundwater to Montezuma Well, a natural spring in Central Arizona, USA: Part 2

    Science.gov (United States)

    Johnson, Raymond H.; DeWitt, Ed; Wirt, Laurie; Manning, Andrew H.; Hunt, Andrew G.

    2012-01-01

    Montezuma Well is a unique natural spring located in a sinkhole surrounded by travertine. Montezuma Well is managed by the National Park Service, and groundwater development in the area is a potential threat to the water source for Montezuma Well. This research was undertaken to better understand the sources of groundwater to Montezuma Well. Strontium isotopes (87Sr/86Sr) indicate that groundwater in the recharge area has flowed through surficial basalts with subsequent contact with the underlying Permian aged sandstones and the deeper, karstic, Mississippian Redwall Limestone. The distinctive geochemistry in Montezuma Well and nearby Soda Springs (higher concentrations of alkalinity, As, B, Cl, and Li) is coincident with added carbon dioxide and mantle-sourced He. The geochemistry and isotopic data from Montezuma Well and Soda Springs allow for the separation of groundwater samples into four categories: (1) upgradient, (2) deep groundwater with carbon dioxide, (3) shallow Verde Formation, and (4) mixing zone. δ18O and δD values, along with noble gas recharge elevation data, indicate that the higher elevation areas to the north and east of Montezuma Well are the groundwater recharge zones for Montezuma Well and most of the groundwater in this portion of the Verde Valley. Adjusted groundwater age dating using likely 14C and δ13C sources indicate an age for Montezuma Well and Soda Springs groundwaters at 5,400–13,300 years, while shallow groundwater in the Verde Formation appears to be older (18,900). Based on water chemistry and isotopic evidence, groundwater flow to Montezuma Well is consistent with a hydrogeologic framework that indicates groundwater flow by (1) recharge in higher elevation basalts to the north and east of Montezuma Well, (2) movement through the upgradient Permian and Mississippian units, especially the Redwall Limestone, and (3) contact with a basalt dike/fracture system that provides a mechanism for groundwater to flow to the surface

  19. Geochemistry and mineralogy

    Energy Technology Data Exchange (ETDEWEB)

    Plecas, I.; Dimovic, S.; Orta, M.M.; Alba, M.D.; Alvero, R.; Becerro, A.I.; Castro, M.A.; Chain, P.; Escudero, A.; Naranjo, M.; Pavon, E.; Trillo, J.M.; Vejsada, J.; Vokal, A.; Zadvernyuk, H.P.; Fedorenko, Y.G.; Zlobenko, B.P.; Koromyslichenko, T.I.; Battaglia, S.; Cervelli, M.; Millot, R.; Girard, J.P.; Missana, T.; Garcia-Gutierrez, M.; Alonso, U.; Muurinen, A.; Carlsson, T.; Chain, P.; Alba, M.D.; Becerro, A.I.; Castro, M.A.; Escudero, A.; Gonzalez-Carrascosa, T.; Hurtado, S.; Pavon, E.; Villa, M.; Bourg, I.C.; Sposito, G.; Bourg, A.C.M.; Marques Fernandes, M.; Rabung, Th.; Dahn, R.; Baeyens, B.; Bradbury, M.H.; Breynaert, E.; Maes, A.; Bruggeman, C.; Maes, I.A.; Vancluysen, J.; Credoz, A.; Bildstein, O.; Jullien, M.; Raynal, J.; Petronin, J.C.; Trotignon, L.; Pokrovsky, O.; Jacquier, P.; Beaucaire, C.; Vuillaume, A.L.; Wittebroodt, Ch.; Ly, J.; Page, J.; Savoye, S.; Pitsch, H.; Jacques, D.; Wang, L.; Galunin, E.; Chain, P.; Alba, M.D.; Vidal, M.; Grandia, F.; Domenech, C.; Arcos, D.; Duro, L.; Bruno, J.; Andre, L.; Pauwels, H.; Azaroual, M.; Albrecht, A.; Romero, M.A.; Aerts, S.; Boven, P.; Van Geet, M.; Boever, P. de; Alonso, U.; Albarran, N.; Missana, T.; Garcia-Gutierrez, M.; Truche, L.; Berger, G.; Guillaume, D.; Jacquot, E.; Tournassat, Ch.; Lerouge, C.; Brendle, J.; Greneche, J.M.; Touzelet, St.; Blanc, Ph.; Gaucher, E.C.; Thoenen, T.; Klinkenberg, M.; Kaufhold, S.; Dohrmann, R.; Siegesmund, S.; Liu, D.J.; Bruggeman, C.; Maes, N.; Weber, T.; Trotignon, L.; Pozo, C.; Bildstein, O.; Combarieu, G. de; Frugier, P.; Menut, D

    2007-07-01

    This session gathers 52 articles (posters) dealing with: the influence of natural sorbents immobilization of spent ion exchange resins in cement; the chemical stability of rare-earth silicate; the mineralogical heterogeneity of Rokle bentonite and radionuclide adsorption: A case study for cesium; the rheological and sorption properties of clay-polymer composites; the clay mineral interactions with leachate solutions in landfills; the lithium isotope fractionation during adsorption onto mineral surfaces; the sorption of Sr{sup 2+} onto mixed smectite / illite clays; Eh and pH in the pore water of compacted bentonite; the chemical interaction of {sup 152}Eu with the clay barrier; the modeling of the acid-base surface chemistry of Montmorillonite; a time resolved laser fluorescence and X-ray absorption spectroscopy study of lanthanide/actinide sorption on clay minerals: influence of carbonate complexation; the structure elucidation and occurrence of Tc(IV) pyrogallol complexes; the geochemistry of Se(0) under boom clay conditions; an experimental and modelling study of pure secondary silicate minerals reactivity in geological CO{sub 2} sequestration conditions; an experimental evaluation of a retention model for major groundwater elements on the Tournemire argillite; modelling the long term interaction of cementitious pore water with Boom clay; the sorption-desorption of radionuclides and analogues in clays suitable for barriers; the modelling of the Redox evolution in the tunnel backfill of a high level nuclear waste repository; the reactivity of nitrates in the different storage compartments of type-b wastes; an investigation into the biodiversity of sulphate reducing bacteria in Boom clay; the colloid generation mechanisms from compacted bentonite under different geochemical conditions; the experimental reduction of aqueous sulphate by hydrogen in the context of the Callovo-Oxfordian argillite; cation exchanged Fe(II) and Sr as compared to other divalent cations

  20. Strontium-90 - ED 4309

    International Nuclear Information System (INIS)

    Ammerich, M.; Frot, P.; Gambini, D.; Gauron, C.; Moureaux, P.; Herbelet, G.; Lahaye, T.; Le Guen, B.; Pihet, P.; Rannou, A.; Vidal, E.

    2012-12-01

    This sheet presents the characteristics of strontium-90, its origin, and its radio-physical and biological properties. It briefly describes its use in nuclear medicine. It indicates its dosimetric parameters for external exposure, cutaneous contamination, and internal exposure due to acute contamination or to chronic contamination. It indicates and comments the various exposure control techniques: ambient dose rate measurement, surface contamination measurement, atmosphere contamination. It addresses the means of protection: premise design, protection against external exposure and against internal exposure. It describes how areas are delimited and controlled within the premises: regulatory areas, controls to be performed. It addresses the personnel classification, training and medical survey. It addresses the issue of wastes and effluents. It briefly recalls the administrative procedures related to the authorization and declaration of possession and use of sealed and unsealed sources. It indicates regulatory aspects related to the transport of strontium-90, describes what is to be done in case of incident or accident (for the different types of contamination or exposure)

  1. Strontium-90 fluoride data sheet

    Energy Technology Data Exchange (ETDEWEB)

    Fullam, H.T.

    1981-06-01

    This report is a compilation of available data and appropriate literature references on the properties of strontium-90 fluoride and nonradioactive strontium fluoride. The objective of the document is to compile in a single source pertinent data to assist potential users in the development, licensing, and use of /sup 90/SrF/sub 2/-fueled radioisotope heat sources for terrestrial power conversion and thermal applications. The report is an update of the Strontium-90 Fluoride Data Sheet (BNWL-2284) originally issued in April 1977.

  2. Zircon Lu-Hf isotope systematics and U-Pb geochronology, whole-rock Sr-Nd isotopes and geochemistry of the early Jurassic Gokcedere pluton, Sakarya Zone-NE Turkey: a magmatic response to roll-back of the Paleo-Tethyan oceanic lithosphere

    Science.gov (United States)

    Karsli, Orhan; Dokuz, Abdurrahman; Kandemir, Raif

    2017-05-01

    The early Mesozoic was a critical era for the geodynamic evolution of the Sakarya Zone as transition from accretion to collision events in the region. However, its complex evolutionary history is still debated. To address this issue, we present new in situ zircon U-Pb ages and Lu-Hf isotope data, whole-rock Sr-Nd isotopes, and mineral chemistry and geochemistry data of plutonic rocks to better understand the magmatic processes. The Gokcedere pluton is mainly composed of gabbro and gabbroic diorite. LA-ICP-MS zircon U-Pb dating reveals that the pluton was emplaced in the early Jurassic (177 Ma). These gabbros and gabbroic diorites are characterized by relatively low SiO2 content of 47.09 to 57.15 wt% and high Mg# values varying from 46 to 75. The samples belong to the calc-alkaline series and exhibit a metaluminous I-type character. Moreover, they are slightly enriched in large ion lithophile elements (Rb, Ba, Th and K) and light rare earth elements and depleted in high field strength elements (Nb and Ti). Gabbroic rocks of the pluton have a depleted Sr-Nd isotopic composition, including low initial 87Sr/86Sr ranging from 0.705124 to 0.705599, relatively high ɛ Nd ( t) values varying from 0.1 to 3.5 and single-stage Nd model ages ( T DM1 = 0.65-0.95 Ga). In situ zircon analyses show that the rocks have variable and positive ɛ Hf ( t) values (4.6 to 13.5) and single-stage Hf model ages ( T DM1 = 0.30 to 0.65 Ga). Both the geochemical signature and Sr-Nd-Hf isotopic composition of the gabbroic rocks reveal that the magma of the studied rocks was formed by the partial melting of a depleted mantle wedge metasomatized by slab-derived fluids. The influence of slab fluids is mirrored by their trace-element characteristics. Trace-element modeling suggests that the primary magma was generated by a low and variable degree of partial melting ( 5-15%) of a depleted and young lithospheric mantle wedge consisting of phlogopite- and spinel-bearing lherzolite. Heat to melt the

  3. Proceedings of the 3. Brazilian Congress on Geochemistry; 1. Congress on Geochemistry from Portuguese Language Countries - Abstracts

    International Nuclear Information System (INIS)

    1991-01-01

    This congress presents topics about geochemistry, including litho-geochemistry, environmental geochemistry, hydro-geochemistry and surface geochemistry. Works on geochronology and nuclear methods in rocks and minerals are also described. (C.G.C.)

  4. Double photoionization of strontium

    Energy Technology Data Exchange (ETDEWEB)

    Sokell, Emma; Grimm, Michael; Sheridan, Paul, E-mail: emma.sokell@ucd.i [School of Physics, University College Dublin, Belfield, Dublin 4 (Ireland)

    2010-02-01

    Resonant triple-differential cross-section (TDCS) measurements have been used to study the double photoionization process in strontium. Two sets of measurements were made at the photon energy of the 4p {yields} 4d resonance. The coplanar geometry was used and the fixed analyser, positioned at -90{sup 0} to the main axis of polarization of the photons, detected electrons with {approx}65% of the available excess energy. The mutual angle between the two electrons had a range just short of 90 {yields} 270{sup 0}. The TDCS exhibit unexpected lobes at a mutual angle of 180{sup 0}. Comparison with other measurements made with the same geometry but with different sharings of the available energy indicate that these TDCS all show the unexpected lobe. Some possible explanations for the lobe are considered.

  5. A distribution of adsorbed forms of cesium 137 and strontium 90 in flood-plain formations of Sozh river

    International Nuclear Information System (INIS)

    Kuznetsov, V.A.; Generalova, V.A.

    1999-01-01

    The distribution of strontium 90 and cesium 137 forms in flood-plain geochemical system 'alluvial deposits - flood-plain turf - humus horizon - soil-source rock', where sorption and colloidal processes play main role in the isotopes migration, was studied. The bulk amount of strontium 90 is presented in adsorbed form in all investigated objects, whereas only 6% of cesium 137 amount in alluvial deposits, flood-plain turf and humus horizon is in adsorbed form. The content of exchange forms of cesium 137 and strontium 90 increases with the depth of the layer. The race of this increase for strontium 90 is large than for cesium 137. The distribution of radionuclides through the different parts of flood-plain of Sozh river has some distinctions due to more lability of adsorbed strontium 90 forms in comparison with cesium 137 ones

  6. Final results on the Jurassic-Cretaceous boundary in the Gresten Klippenbelt (Austria): Macro-, micro-, nannofossils, isotopes, geochemistry, susceptibility, gamma-log and palaeomagnetic data as environmental proxies of the early Penninic Ocean history

    Science.gov (United States)

    Lukeneder, A.; Halásová, E.; Kroh, A.; Mayrhofer, S.; Pruner, P.; Reháková, D.; Schnabl, P.; Sprovieri, M.

    2009-04-01

    -6 SI and the intensity of the natural remanent magnetization (NRM) varies between 31 and 615×10-6 A/m. The samples display a two- to three-component remanence. The average sampling density for the whole section was around two samples per 1 m of true thickness of limestone strata in these preliminary results. The next step of investigation will be to precisely determine the boundaries of magnetozones M19 and M20 including narrow reverse subzones with the high resolution sampling density for the whole section. Stable isotope data (C, O, Sr). High-resolution reconstruction of the carbon cycle, by isotope stratigraphy, is the key for drawing conclusions on the palaeooceanography of the Nutzhof area. The approach using oxygen isotope analysis, by constraining diagenesis impacts, will yield a picture of the Lower Cretaceous palaeoclimatology here. The investigations on istopes will be rigorously linked and networked with measurements and results of cyclostratigraphy and lithostratigraphy. C-istopes are extremely important calibration tools between ammonoids and magnetostratigraphy (Henning et al. 1999). Cyclostratigraphy is crucial in comparing the lithologic appearance of different units and the carbon isotope records. A detailed cyclostratigraphic reconstruction of the record will be carried out by comparing (1) the results obtained by time series analysis of the collected faunal and isotope proxy records with (2) the reconstructed lithologic cycle patterns of the studied sedimentary sections. A first-order floating cyclostratigraphy will be refined using a tentative calibration of the record to the available numerical solutions of the insolation curve. This approach should provide an absolute age for the different stratigraphic events recognised throughout the record. Gamma-log and Geochemistry. We conducted geochemical analyses of the carbonate, sulphur and organic carbon content in the limestones and marls of the different lithological units. The gamma log measures the

  7. The genetics of geochemistry

    OpenAIRE

    Croal, Laura R.; Gralnick, Jeffrey A.; Malasarn, Davin; Newman, Dianne K.

    2004-01-01

    Bacteria are remarkable in their metabolic diversity due to their ability to harvest energy from myriad oxidation and reduction reactions. In some cases, their metabolisms involve redox transformations of metal(loid)s, which lead to the precipitation, transformation, or dissolution of minerals. Microorganism/mineral interactions not only affect the geochemistry of modern environments, but may also have contributed to shaping the near-surface environment of the early Earth. For example, bacter...

  8. Preparation and use of polymeric materials containing hydrophobic anions and plasticizers for separation of cesium and strontium

    International Nuclear Information System (INIS)

    Abney, K.D.; Kinkead, S.A.; Mason, C.F.V.; Rais, J.

    1997-01-01

    Preparation and use is described for polymeric materials containing hydrophobic anions and plasticizers for extraction of cesium and strontium. The use of polymeric materials containing plasticizers which are solvents for hydrophobic anions such as derivatives of cobalt dicarbollide or tetraphenylborate which are capable of extracting cesium and strontium ions from aqueous solutions in contact with the polymeric materials, is described. The polymeric material may also include a synergistic agent for a given ion like polyethylene glycol or a crown ether, for removal of radioactive isotopes of cesium and strontium from solutions of diverse composition and, in particular, for solutions containing large excess of sodium nitrate

  9. Geochemistry of impact glasses and target rocks from the Zhamanshin impact structure, Kazakhstan: Implications for mixing of target and impactor matter

    Czech Academy of Sciences Publication Activity Database

    Jonášová, Šárka; Ackerman, Lukáš; Žák, Karel; Skála, Roman; Ďurišová, Jana; Deutsch, A.; Magna, T.

    2016-01-01

    Roč. 190, 1 October (2016), s. 239-264 ISSN 0016-7037 R&D Projects: GA ČR GA13-22351S Institutional support: RVO:67985831 Keywords : impact glass * irghizites * geochemistry * meteoritic component * siderophile elements * osmium isotopes * Zhamanshin Subject RIV: DD - Geochemistry Impact factor: 4.609, year: 2016

  10. Study of the geochemistry of the cosmogenic isotope {sup 10}Be and the stable isotope {sup 9}Be in oceanic environment. Application to marine sediment dating; Etude de la geochimie de l`isotope cosmogenique {sup 10}Be et de son isotope stable {sup 9}Be en milieu oceanique. Application a la datation des sediments marins

    Energy Technology Data Exchange (ETDEWEB)

    Bourles, D

    1988-01-01

    The radioisotope {sup 10}Be is formed by spallation reactions in the atmosphere. It is transferred to the oceans in soluble form by precipitation and dry deposition. The stable isotope {sup 9}Be comes from erosion of soils and rocks in the Earth`s crust. It is transported by wind and rivers and introduced to the oceans probably in both soluble and insoluble form. {sup 9}Be was measured by atomic absorption spectrometry and {sup 10}Be by A.M.S. The distribution of {sup 10}Be and {sup 9}Be between each phase extracted and the {sup 10}Be/{sup 9}Be ratios associated were studied in recent marine sediments from Atlantic, Pacific, Indian oceans and Mediterranean sea. The results show that for beryllium the two essential constituent phases of marine sediments are: - the authigenic phase incorporates the soluble beryllium and the detritic phase. The {sup 10}Be/{sup 9}Be ratio associated with the authigenic fraction varies with location. This suggests that the residence time of beryllium in the soluble phase is lower or comparable to the mixing time of the oceans. The evolution with time of the authigenic {sup 10}Be/{sup 9}Be ratio is discussed.

  11. Polymeric strontium ranelate nonahydrate

    Directory of Open Access Journals (Sweden)

    Kenny Stahl

    2011-04-01

    Full Text Available The title compound, poly[[μ-aqua-tetraaqua{μ-5-[bis(carboxylatomethylamino]-3-carboxylatomethyl-4-cyanothiophene-2-carboxylato}distrontium(II] tetrahydrate], [Sr2(C12H6N2O8S(H2O5]·3.79H2O, crystallizes with nine- and eight-coordinated Sr2+ cations. They are bound to seven of the eight ranelate O atoms and five of the water molecules. The SrO8 and SrO9 polyhedra are interconnected by edge-sharing, forming hollow layers parallel to (011. The layers are, in turn, interconnected by ranelate anions, forming a metal–organic framework (MOF structure with channels along the a axis. The four water molecules not coordinated to strontium are located in these channels and hydrogen bonded to each other and to the ranelates. Part of the water H atoms are disordered. The compound dehydrates very easily and 0.210 (4 water molecules out of nine were lost during crystal mounting causing additional disorder in the water structure.

  12. Photostriction of strontium ruthenate

    KAUST Repository

    Wei, Tzu-Chiao

    2017-04-24

    Transition metal oxides with a perovskite crystal structure exhibit a variety of physical properties associated with the lattice. Among these materials, strontium ruthenate (SrRuO3) displays unusually strong coupling of charge, spin and lattice degrees of freedom that can give rise to the photostriction, that is, changes in the dimensions of material due to the absorption of light. In this study, we observe a photon-induced strain as high as 1.12% in single domain SrRuO3, which we attribute to a nonequilibrium of phonons that are a result of the strong interaction between the crystalline lattice and electrons excited by light. In addition, these light-induced changes in the SrRuO3 lattice affect its electrical resistance. The observation of both photostriction and photoresistance in SrRuO3 suggests the possibility of utilizing the mechanical and optical functionalities of the material for next-generation optoelectronics, such as remote switches, light-controlled elastic micromotors, microactuators and other optomechanical systems.

  13. PETROCHEMISTRY, Pb ISOTOPE SYSTEMATICS, AND ...

    African Journals Online (AJOL)

    The petrology, geochemistry, geotectonic setting and common Pb isotope model ages for the granite gneisses in Ilesha schist belt have been studied and presented in this paper. These gneisses, apart from the normal rock-forming silicates, contain apatite, monazite, ilmenite and zircon in trace amounts. The occurrence of ...

  14. Sorption of strontium on uranyl peroxide: implications for a high-level nuclear waste repository.

    Science.gov (United States)

    Sureda, Rosa; Martínez-Lladó, Xavier; Rovira, Miquel; de Pablo, Joan; Casas, Ignasi; Giménez, Javier

    2010-09-15

    Strontium-90 is considered the most important radioactive isotope in the environment and one of the most frequently occurring radionuclides in groundwaters at nuclear facilities. The uranyl peroxide studtite (UO2O2 . 4H2O) has been observed to be formed in spent nuclear fuel leaching experiments and seems to have a relatively high sorption capacity for some radionuclides. In this work, the sorption of strontium onto studtite is studied as a function of time, strontium concentration in solution and pH. The main results obtained are (a) sorption is relatively fast although slower than for cesium; (b) strontium seems to be sorbed via a monolayer coverage of the studtite surface, (c) sorption has a strong dependence on ionic strength, is negligible at acidic pH, and increases at neutral to alkaline pH (almost 100% of the strontium in solution is sorbed above pH 10). These results point to uranium secondary solid phase formation on the spent nuclear fuel as an important mechanism for strontium retention in a high-level nuclear waste repository (HLNW). Copyright 2010 Elsevier B.V. All rights reserved.

  15. Strontium 90 fallout prediction

    International Nuclear Information System (INIS)

    Sarmiento, J.L.; Gwinn, E.

    1986-01-01

    An empirical formula is developed for predicting monthly sea level strontium 90 fallout (F) in the northern hemisphere as a function of time (t), precipitation rate (P), latitude (phi), longitude (lambda), and the sea level concentration of stronium 90 in air (C): F(lambda, phi, t) = C(t, phi)[v /sub d/(phi) + v/sub w/(lambda, phi, t)], where v/sub w/(lambda, phi, t) = a(phi)[P(lambda, phi, t)/P/sub o/]/sup b//sup (//sup phi//sup )/ is the wet removal, v/sub d/(phi) is the dry removal and P 0 is 1 cm/month. The constants v/sub d/, a, and b are determined as functions of latitude by fitting land based observations. The concentration of 90 Sr in air is calculated as a function of the deseasonalized concentration at a reference latitude (C-bar/sub r//sub e//sub f/), the ratio of the observations at the latitude of interest to the reference latitude (R), and a function representing the seasonal trend in the air concentration (1 + g): C-bar(t, phi) = C/sub r//sub e//sub f/(t)R(phi)[1 + g(m, phi)]; m is the month. Zonal trends in C are shown to be relatively small. This formula can be used in conjuction with precipitation observations and/or estimates to predict fallout in the northern hemisphere for any month in the years 1954 to 1974. Error estimates are given; they do not include uncertainty due to errors in precipitation data

  16. Constraints on the nature of the projectile using siderophile elements and triple-oxygen isotopes: Zhamanshin impact structure, Kazakhstan

    Czech Academy of Sciences Publication Activity Database

    Jonášová, Šárka; Ackerman, Lukáš; Žák, Karel; Skála, Roman; Magna, T.; Pack, A.; Deutsch, A.

    2016-01-01

    Roč. 51, SI, Supplement 1 (2016), A358-A358 ISSN 1086-9379. [Annual Meeting of the Meteoritical Society /79./. 07.08.2016-12.08.2016, Berlin] Institutional support: RVO:67985831 Keywords : impact glass * irghizites * geochemistry * meteoritic component * siderophile elements * osmium isotopes * triple-oxygen Isotopes * Zhamanshin Subject RIV: DD - Geochemistry

  17. Geochemical and isotopic determination of deep groundwater contributions and salinity to the shallow groundwater and surface water systems, Mesilla Basin, New Mexico, Texas, and Mexico

    Science.gov (United States)

    Robertson, A.; Carroll, K. C.; Kubicki, C.; Purtshert, R.

    2017-12-01

    The Mesilla Basin/Conejos-Médanos aquifer system, extending from southern New Mexico to Chihuahua, Mexico, is a priority transboundary aquifer under the 2006 United States­-Mexico Transboundary Aquifer Assessment Act. Declining water levels, deteriorating water quality, and increasing groundwater use by municipal, industrial, and agricultural users on both sides of the international border raise concerns about long-term aquifer sustainability. Relative contributions of present-day and "paleo" recharge to sustainable fresh groundwater yields has not been determined and evidence suggests that a large source of salinity at the distal end of the Mesilla Basin is saline discharge from deep groundwater flow. The magnitude and distribution of those deep saline flow paths are not determined. The contribution of deep groundwater to discharge and salinity in the shallow groundwater and surface water of the Mesilla Basin will be determined by collecting discrete groundwater samples and analyzing for aqueous geochemical and isotopic tracers, as well as the radioisotopes of argon and krypton. Analytes include major ions, trace elements, the stable isotopes of water, strontium and boron isotopes, uranium isotopes, the carbon isotopes of dissolved inorganic carbon, noble gas concentrations and helium isotope ratios. Dissolved gases are extracted and captured from groundwater wells using membrane contactors in a process known as ultra-trace sampling. Gas samples are analyzed for radioisotope ratios of krypton by the ATTA method and argon by low-level counting. Effectiveness of the ultra-trace sampling device and method was evaluated by comparing results of tritium concentrations to the krypton-85 content. Good agreement between the analyses, especially in samples with undetectable tritium, indicates that the ultra-trace procedure is effective and confirms that introduction of atmospheric air has not occurred. The geochemistry data indicate a complex system of geochemical

  18. Highly siderophile element geochemistry of peridotites and pyroxenites from Horní Bory, Bohemian Massif: Implications for HSE behaviour in subduction-related upper mantle

    Czech Academy of Sciences Publication Activity Database

    Ackerman, Lukáš; Pitcher, L.; Strnad, L.; Puchtel, I. S.; Jelínek, E.; Walker, R. J.; Rohovec, Jan

    2013-01-01

    Roč. 100, č. 1 (2013), s. 158-175 ISSN 0016-7037 R&D Projects: GA AV ČR KJB300130902 Institutional research plan: CEZ:AV0Z30130516 Institutional support: RVO:67985831 Keywords : alloy * high pressure * high temperature * igneous geochemistry * isotopic composition * mass balance * nappe * osmium isotope * peridotite * petrography * platinum group element * precipitation (chemistry) * pyroxenite * siderophile element * subduction * sulfide * upper mantle Subject RIV: DD - Geochemistry Impact factor: 4.250, year: 2013

  19. Lectures in isotope geology

    International Nuclear Information System (INIS)

    Jaeger, E.; Hunziker, J.C.

    1979-01-01

    Designed for a introductory course in geochronology and the geochemistry of stable isotopes, this text has been written by recognized experts in the field. Emphasis is on the interpretation and on applications, and examples of these are offered along with each technique. Extraterrestrial applications have been avoided and the treatment of pure experimentation has been kept at a minimum. This text will be appreciated by geologists who want to learn more about methods used in isotope geology, how they can be applied, and how to gauge their usefulness. (orig.) [de

  20. Geochemistry of natural technetium and plutonium

    International Nuclear Information System (INIS)

    Curtis, D.B.; Cappis, J.H.; Perrin, R.E.; Rokop, D.J.

    1987-01-01

    Technetium and plutonium in unprocessed nuclear reactor wastes are major concerns with regard to their containment in the geologic environment. Both nuclides have long half-lives; therefore, they will exist long after engineered barriers can be considered reliable. Consequently, strategies for the containment of these two elements depend on their retention in the geologic barrier until they have decayed to innocuous levels. Because these are the rarest elements in nature, there have been few direct observations of their geochemical behavior; predictions concerning their fate in the repository are based on properties that can be observed in the laboratory. The authors are attempting to complement the laboratory work by studying the geochemistry of natural plutonium and technetium. Ratios of anthropogenic to naturally occurring isotopes are discussed

  1. Spectroscopy of strontium Rydberg states using electromagnetically induced transparency

    International Nuclear Information System (INIS)

    Mauger, S; Millen, J; Jones, M P A

    2007-01-01

    We report on the all-optical detection of Rydberg states in an effusive atomic beam of strontium atoms using electromagnetically induced transparency (EIT). Using narrow-linewidth CW lasers we obtain an EIT linewidth of 5 MHz. To illustrate the high spectroscopic resolution offered by this method, we have measured isotope shifts of the 5s18d 1 D 2 and 5s19s 1 S 0 Rydberg states. This technique could be applied to high-resolution, non-destructive measurements of ultra-cold Rydberg gases and plasmas. (fast track communication)

  2. Experimental study of strontium sorption on fissure filling material

    Energy Technology Data Exchange (ETDEWEB)

    Eriksen, T E; Cui, Daqing [Royal Institute of Technology, Stockholm (Sweden). Dept. of Chemistry

    1994-12-01

    We have carried out a comparative study of sorption and desorption of strontium in groundwater on separated magnetic and size fractions of fissure filling material taken from natural fissures in granitic rock. Complete reversibility of the sorption process was demonstrated by identical Freundlich isotherms, isotopic exchangeability and pH dependence of the distribution coefficients Rd. The sorption was found to be strongly pH dependent in the range 3-11. The pH effect can be accommodated in the sorption model by considering the surface areas and surface charges of the minerals in the fissure filling material. 20 refs, 9 figs, 3 tabs.

  3. Experimental study of strontium sorption on fissure filling material

    International Nuclear Information System (INIS)

    Eriksen, T.E.; Cui, Daqing

    1994-12-01

    We have carried out a comparative study of sorption and desorption of strontium in groundwater on separated magnetic and size fractions of fissure filling material taken from natural fissures in granitic rock. Complete reversibility of the sorption process was demonstrated by identical Freundlich isotherms, isotopic exchangeability and pH dependence of the distribution coefficients Rd. The sorption was found to be strongly pH dependent in the range 3-11. The pH effect can be accommodated in the sorption model by considering the surface areas and surface charges of the minerals in the fissure filling material. 20 refs, 9 figs, 3 tabs

  4. Determinação da composição isotópica de estrôncio em águas naturais: exemplos de sua aplicação em águas subsuperficiais da zona costeira na região Bragantina-PA Determination of strontium isotopic composition in natural waters: examples of application in subsurface waters of the coastal zone of Bragantina region, Pará

    Directory of Open Access Journals (Sweden)

    Adriana Oliveira Bordalo

    2007-08-01

    Full Text Available Analytical procedures used for determining the concentrations and isotope composition of strontium in subsurface waters, by mass spectrometry, are described. Sampling was performed in coastal plateaus, salt marsh and mangrove environments in the coastal region of Pará. Coastal plateau waters have delta87Sr between 1.51 and 6.26‰ and Sr concentration bellow 58 ppb. Salt marsh waters show delta87Sr between 0.55 and 0.90‰ and Sr concentration between 93 and 114 ppm, while mangrove waters have delta87Sr‰ around zero and Sr concentration above 15 ppm. Differences in the 87Sr/86Sr ratio in these subsurface waters are detected, as well as seasonal variations in the coastal pleteau waters.

  5. Dissolved strontium and calcium levels in the tropical Indian Ocean

    Science.gov (United States)

    Steiner, Zvi; Sarkar, Amit; Turchyn, Alexandra

    2017-04-01

    Measurements of seawater alkalinity and dissolved calcium concentrations along oceanic transects are often used to calculate calcium carbonate precipitation and dissolution rates. Given that the distribution coefficient of strontium in CaCO3 varies greatly between different groups of organisms, adding precise measurements of dissolved strontium concentrations provides opportunities to also track relative contributions of these different groups to the regional CaCO3 cycle. However, there are several obstacles to this approach. These obstacles include unresolved systematic discrepancies between seawater calcium and alkalinity data, very large analytical noise around the calcium concentration measurements and the unconstrained role of acantharia (radiolarian precipitating SrSO4 skeletons) in the marine strontium cycle. During the first cruise of the second International Indian Ocean Expedition (IIOE-2) water samples were collected along 67°E from 9°N to 5°S to explore the dissolution rate of calcium carbonate in the water. The dissolution rate can be calculated by combining measurements of water column potential alkalinity with calcium and strontium concentrations measured by ICP-OES and calcium concentration measurements using isotope dilution thermal ionization mass spectrometry (ID-TIMS). CaCO3 mineral saturation state calculated using pH and total alkalinity suggests that along 67°E, the aragonite saturation horizon lays at depth of 500 m on both sides of the equator. Across the cruise transect, dissolved strontium concentrations increase by 2-3% along the thermocline suggesting rapid recycling of strontium rich phases. This is particularly evident just below the thermocline at 8-9°N and below 1000 m water depth, south of the equator. The deep, southern enrichment in strontium does not involve a change in the Sr/Ca ratio, suggesting that this strontium enrichment is related to CaCO3 dissolution. In contrast, in the intermediate waters of the northern part of

  6. Innovation in metrology: fast automated radiochemical separation and measurement for strontium 89 and 90

    Energy Technology Data Exchange (ETDEWEB)

    Augeray, C.; Galliez, K.; Mouton, M.; Tarlette, L.; Loyen, J.; Fayolle, C.; Gleizes, M. [Institut de Radioprotection et de Surete Nucleaire - IRSN (France)

    2014-07-01

    Measuring radioactivity in the food and for radiological monitoring of the environment around Nuclear Facilities or mining sites requires the quantification of the radioactive isotopes present in the different compartments (liquids or solids), especially of the beta emitters. Strontium 89 and 90, both pure beta emitters are radioactive isotopes of interest. Because of their toxicity and the similarity of their chemical and physical behavior with calcium, these elements may be found through the food chain. After the Fukushima accident, the necessity of quantifying quickly radioactive isotopes such as strontium 89 and 90 appeared. The technique we are going to present concerns the determination of the activity concentration of strontium 89 and 90 in water, according to the {sup 89}Sr/{sup 90}Sr ratio. It consists of two stages: the chemical separation by ionic chromatography and the measurement of the activity concentration of strontium 89 and 90 by Cerenkov Effect. The automated separation has been developed and allows isolating the isotopes of strontium in particular the radioactive ones: strontium 89 and 90. The separation can be done within one hour. It was realized from the adaptation of existing analytical chemistry equipments with on-line couplings. The protocol of separation is based on the use of ions exchange columns of Ionic chromatography not as a separation and measurement technique of the cation but only as a separation technique. At the release time of the ion to be quantified, a fraction collector allows its recovery. The test portion is then analyzed with a liquid scintillation counter (LSC). The activity concentration is measured by Cerenkov Effect on a quenched sample. The quenching is realized by applying a thin colored film on the sample vial. This color quench is used to make strontium 90 counts disappear on the LS spectrum. This way, only yttrium 90 ingrowth and strontium 89 decay are measured (E{sup 90}Sr < E{sup 89}Sr < E{sup 90}Y

  7. Studies of cesium and strontium migration in unconsolidated Canadian geological materials

    International Nuclear Information System (INIS)

    Gillham, R.W.; Lindsay, L.E.; Reynolds, W.D.; Kewen, T.J.; Cherry, J.A.; Reddy, M.R.

    1981-06-01

    Distribution coefficients (Ksub(d)) were measured for cesium and strontium in 16 samples of Canadian unconsolidated geological materials. The samples were collected to cover a wide range of grain size, clay-mineral composition, cation exchange capacity and carbonate mineral content. Distribution coefficients ranged between 10 2 and 2.0 x 10 4 ml/g for cesium and between 2.5 and 10 2 ml/g for strontium, indicating that most unconsolidated geological materials have a substantial ability to retard the migration of cesium, while strontium could generally be expected to be somewhat more mobile. The measured K values were not significantly correlated with the measured soil properties, but appeared to be significantly affected by the background concentration of stable isotopes of the respective radionuclides

  8. Age of underground waters: isotopes contribution

    International Nuclear Information System (INIS)

    Chery, L.; Olive, Ph.

    2006-01-01

    Does water has an age? The age of underground waters can be the duration of their underground travel between their infiltration inside the ground and their captation at a spring or a drilled well. The isotopic geochemistry comes to the support of classical geochemistry to estimate these residence times. Radio-isotopes, like tritium for young waters or carbon 14 for old waters, are used as chronometers to interpret the recharge ways, the flow mechanisms and the residence times of underground waters. Their use is presented in this article with some theoretical recalls and some examples of application. (J.S.)

  9. Combined transuranic-strontium extraction process

    Science.gov (United States)

    Horwitz, E. Philip; Dietz, Mark L.

    1992-01-01

    The transuranic (TRU) elements neptunium, plutonium and americium can be separated together with strontium from nitric acid waste solutions in a single process. An extractant solution of a crown ether and an alkyl(phenyl)-N,N-dialkylcarbanylmethylphosphine oxide in an appropriate diluent will extract the TRU's together with strontium, uranium and technetium. The TRU's and the strontium can then be selectively stripped from the extractant for disposal.

  10. Ion exchange of strontium on synthetic hydroxyapatite

    International Nuclear Information System (INIS)

    Lazic, S.; Vukovic, Z.

    1991-01-01

    Adsorption of strontium ions on synthetic hydroxyapatite was examined using both batch and column methods. The apatite was prepared from aqueous solutions and characterized by standard analytical methods. The sample obtained had characteristics of well crystallized stoichiometric hydroxyapatite. The experimental data for sorption of strontium can be very well fitted with Langmuir's adsorption isotherm. It was found that sorption occurs by an ion exchange reaction between strontium ions in solution and calcium ions in apatite. (author) 14 refs.; 5 figs.; 1 tab

  11. Kinetics of strontium sorption in calcium phosphate

    International Nuclear Information System (INIS)

    Bacic, S.; Komarov, V.F.; Vukovic, Z.

    1989-01-01

    Kinetics of strontium sorption by highly dispersed solids: tricalcium phosphate (Ca 3 (PO 4 ) 2 , TCP) and hydroxyapatite (Ca 5 (PO 4 ) 3 )H, HAP) were investigated. Analysis of sorption data was made taking into consideration composition and morphology of ultra micro particles. Conclusion is that the isomorphous strontium impurity is structurally sensitive element for calcium phosphate. It was determined that the beginning of strontium desorption corresponds to the beginning of transformation of the TCP - HAP (author)

  12. Optical lattice clock with Strontium atoms

    International Nuclear Information System (INIS)

    Baillard, X.

    2008-01-01

    This thesis presents the latest achievements regarding the optical lattice clock with Strontium atoms developed at LNE-SYRTE. After a review of the different types of optical clocks that are currently under development, we stress on the concept of optical lattice clock which was first imagined for Sr 87 using the 1 S 0 → 3 P 0 transition. We exhibit the features of this atom, in particular the concept of magic wavelength for the trap, and the achievable performances for this kind of clock. The second part presents the experimental aspects, insisting particularly on the ultra-stable laser used for the interrogation of the atoms which is a central part of the experiment. Among the latest improvements, an optical pumping phase and an interrogation phase using a magnetic field have been added in order to refine the evaluation of the Zeeman effect. Finally, the last part presents the experimental results. The last evaluation of the clock using Sr 87 atoms allowed us to reach a frequency accuracy of 2.6*10 -15 and a measurement in agreement with the one made at JILA (Tokyo university) at the 10 -15 level. On another hand, thanks to recent theoretical proposals, we made a measurement using the bosonic isotope Sr 88 by adapting the experimental setup. This measurement represents the first evaluation for this type of clock, with a frequency accuracy of 7*10 -14 . (author)

  13. Strontium sorption on Savannah River Plant soils

    International Nuclear Information System (INIS)

    Hoeffner, S.L.

    1984-12-01

    A laboratory study of strontium-85 sorption was conducted using Savannah River Plant soil and groundwater from the low-level waste burial ground. Systematic variation of soil and water composition indicates that strontium sorption is most strongly a function of pH. Changes in clay content and in K + , Ca 2+ , or Mg 2+ concentrations influence strontium sorption indirectly through the slight pH changes which result. The ions Na + , Cl - , and NO 3 - have no effect. Ferrous ion, added to groundwater to simulate the conditions of water at the bottom of waste trenches, did not account for low strontium sorption observed with some trench waters

  14. Optimization of a Strontium Aluminate

    Energy Technology Data Exchange (ETDEWEB)

    Bone, Alexandria N. [Maryville College, TN (United States)

    2017-08-01

    Strontium aluminate with Eu2+ and Dy3+ has been at the forefront of emerging applications for storage phosphors since its discovery in 1996. In this study, the emission intensity and luminescence lifetime of SrAl2O4: Eu2+, Dy3+ were enhanced by partial substitution of Ca2+ into Sr2+ sites in the matrix.

  15. Equilibrium sorption of cobalt, cesium, and strontium on Bandelier Tuff: analysis of alternative mathematical modeling

    International Nuclear Information System (INIS)

    Polzer, W.L.; Fuentes, H.R.; Essington, E.H.; Roensch, F.R.

    1985-01-01

    Sorption isotherms are derived from batch equilibrium data for cobalt, cesium and strontium on Bandelier Tuff. Experiments were conducted at an average temperature of 23 0 C and equilibrium was defined at 48 hours. The solute concentrations ranged from 0 to 500 mg/L. The radioactive isotopes 60 Co, 137 Cs, and 85 Sr were used to trace the sorption of the stable solutes. The Linear, Langmuir, Freundlich and a Modified Freundlich isotherm equations are evaluated. The Modified Freundlich isotherm equation is validated as a preferred general mathematical tool for representing the sorption of the three solutes. The empirical constants derived from the Modified Freundlich isotherm equation indicate that under dynamic flow conditions strontium will move most rapidly and cobalt least rapidly. On the other hand, chemical dispersion will be greatest for cesium and least for strontium. Hill Plots of the sorption data suggest that in the region of low saturation sorption of all three solutes is impeded by interactions among sorption sites; cobalt exhibits the greatest effect of interactions and strontium shows only a minimal effect. In the saturation region of 50% or more, sorption of cobalt is enhanced slightly by interactions among sorption sites whereas sorption of cesium and strontium appears to be independent of site interactions. 9 references, 4 figures, 2 tables

  16. Growth Rates, Stable Oxygen Isotopes (18O), and Strontium (Sr/Ca) Composition in Two Species of Pacific Sclerosponges (Acanthocheatetes wellsi and Astrosclera willeyana) with 18O Calibration and Application to Paleoceanography

    Energy Technology Data Exchange (ETDEWEB)

    Grottoli, A.; Adkins, J; Panero, W; Reaman, D; Moots, K

    2010-01-01

    The isotopic and elemental composition of sclerosponge skeletons is used to reconstruct paleoceanographic records. Yet few studies have systematically examined the natural variability in sclerosponge skeletal {delta}{sup 18}O, growth, and Sr/Ca, and how that may influence the interpretation of sclerosponge proxy records. Here, we analyzed short records in seven specimens of Acanthocheatetes wellsi (high-Mg calcite, 21 mol% Mg) from Palau, four A. wellsi (high-Mg calcite, 21 mol% Mg) from Saipan, and three Astrosclera willeyana (aragonite) sclerosponges from Saipan, as well as one long record in an A. wellsi specimen from Palau spanning 1945-2001.5. In Saipan, species-specific and mineralogical effects appear to have a negligible effect on sclerosponge {delta}{sup 18}O, facilitating the direct comparison of {delta}{sup 18}O records between species at a given location. At both sites, A. wellsi {delta}{sup 18}O and growth rates were sensitive to environmental conditions, but Sr/Ca was not sensitive to the same conditions. High-resolution {delta}{sup 18}O analyses confirmed this finding as both A. wellsi and A. willeyana deposited their skeleton in accordance with the trends in isotopic equilibrium with seawater, though with a 0.27{per_thousand} offset in the case of A. willeyana. In the high-Mg-calcite species A. wellsi, Mg may be interfering with Sr incorporation into the skeleton. On multidecadal timescales, A. wellsi sclerosponge {delta}{sup 18}O in Palau tracked the Southern Oscillation Index variability post-1977, but not pre-1977, coincident with the switch in the Pacific Decadal Oscillation (PDO) at {approx}1976. This suggests that water mass circulation in the region is influenced by El Nino-Southern Oscillation variability during positive PDO phases, but not during negative ones.

  17. Research on the possibility of separation of the small amounts of calcium from strontium during crystallization of their nitrates in the system acetic acid-water

    International Nuclear Information System (INIS)

    Hubicki, W.; Piskorek, M.

    1976-01-01

    Co-crystallization of the calcium nitrate and strontium nitrate from solutions of acetic acid at room temperature and boiling point were investigated. The process of crystallization was studied, using radioactive calcium isotope Ca 45 of 153 day semi-stability period. The presented investigations show that high effects of purifying strontium nitrate from small amounts of calcium can be obtained during crystallization of these nitrates from the system CH 3 COOH-H 2 O. This method was applied for obtaining strontium nitrate of high purity. (author)

  18. Uranium Geochemistry in Hypersaline Soda Lakes in Eastern Mongolia

    Science.gov (United States)

    Linhoff, B. S.; Bennett, P.; Puntsag, T.

    2007-12-01

    Extremely high concentrations of uranium were discovered in water samples from hypersaline soda lakes in eastern Mongolia. The origin and fate of uranium in these lakes was examined using geochemical analyses and modeling, using samples collected from five lakes, six wells and one stream. Samples were analyzed for strontium and uranium isotopes, cations and trace metals, anions, alkalinity, and unstable field parameters. The lakes are small, shallow (chlorine to bromine ratios implying groundwater discharges to lake water and is subsequently evaporated. Evaporation is intense with lake waters having average chlorine concentrations 300 times that of well waters. Uranium in well samples is higher than typical for shallow groundwaters (7-101ppb) suggesting discharging groundwater as a probable source of uranium in lake water. Concentrations of uranium in lake water ranges from 57-14,900ppb making these lakes possibly the highest naturally occurring uranium concentration reported. Lake water alkalinity is strongly correlated to uranium abundance suggesting uranium is complexed with carbonate as the aqueous species UO2CO3. Consequently, the extremely high alkalinity of the most alkaline lake (pH = 9.8, 1288.8 meq alk/L) also has the highest uranium concentrations. Stable strontium isotopes were used to assess the degree of water rock interactions and the presence of 90Sr was checked for to test the possibility of input of nuclear fallout. 90Sr was not detected in lake water samples suggesting the high uranium is of natural origins. A large difference in the 87Sr/86Sr ratio was found between groundwater and lake water samples. Groundwater samples displayed large variation in the 87Sr/86Sr ratio (0.70612-0.709776) whereas lake water samples averaged a high radiogenic ratio (0.709432). The large variation in the strontium isotopes in groundwater samples suggests varying degrees of water rock interactions, however the least radiogenic samples likely are derived from

  19. Recent development in isotope ratio mass spectrometry

    International Nuclear Information System (INIS)

    Platzner, I.

    1992-01-01

    Within the limited of this review the following topics will be briefly discussed: a) Accuracy, precision, internal relative standard deviation (RISD) and external relative standard deviation (RESD) of isotope ratio measurements. With advanced instrumentation and use of standard reference materials, high accuracy and RESD = 0.002% (or better) may be achieved; b) The advantages of modern automatic isotope ratio mass spectrometer are briefly described. Computer controlled operation and data acquisition, and multiple ion collection are the recent important improvement; c) The isotopic fractionation during the course of isotope ratio measurement is considered as a major source of errors in thermal ionization of metallic elements. The phenomenon in strontium, neodymium, uranium, lead and calcium and methods to correct the measured data are discussed; d) Applications of isotope ratio mass spectrometry in atomic weight determinations, the isotope dilution technique, isotope geology, and isotope effects in biological systems are described together with specific applications in various research and technology area. (author)

  20. A review of volatile compounds in tektites, and carbon content and isotopic composition of moldavite glass

    Czech Academy of Sciences Publication Activity Database

    Žák, Karel; Skála, Roman; Řanda, Zdeněk; Mizera, Jiří

    2012-01-01

    Roč. 47, č. 6 (2012), s. 1010-1028 ISSN 1086-9379 R&D Projects: GA ČR GA205/09/0991 Institutional research plan: CEZ:AV0Z30130516; CEZ:AV0Z10480505 Keywords : moldavites * geochemistry * ries * carbon stable isotopes * moldavites (Germany) Subject RIV: DD - Geochemistry Impact factor: 2.800, year: 2012

  1. Chronostatigraphy of limistone sequency of north Brazilian coast based on data from stronium isotope

    International Nuclear Information System (INIS)

    Takaki, T.; Rodrigues, R.

    1987-01-01

    The strontium isotope composition of marine limestones can be a valuable tool for stratigraphic correlation, in addition to other techniques usually employed for this purpose. The technique can render particularly important in sequences where the fossil assemblage do not present good stratigraphic resolution. As examples, data from Mesozoic and Cenozoic limestone sequences of north Brazilian coast are here presented. Data on strontium isotope composition are compared to those obtained by De Paolo and Ingram in another geographic locations. (author) [pt

  2. SRP baseline hydrogeologic investigation: Aquifer characterization. Groundwater geochemistry of the Savannah River Site and vicinity

    Energy Technology Data Exchange (ETDEWEB)

    Strom, R.N.; Kaback, D.S.

    1992-03-31

    An investigation of the mineralogy and chemistry of the principal hydrogeologic units and the geochemistry of the water in the principal aquifers at Savannah River Site (SRS) was undertaken as part of the Baseline Hydrogeologic Investigation. This investigation was conducted to provide background data for future site studies and reports and to provide a site-wide interpretation of the geology and geochemistry of the Coastal Plain Hydrostratigraphic province. Ground water samples were analyzed for major cations and anions, minor and trace elements, gross alpha and beta, tritium, stable isotopes of hydrogen, oxygen, and carbon, and carbon-14. Sediments from the well borings were analyzed for mineralogy and major and minor elements.

  3. Strontium 90 in Swedish dairy milk 1978

    International Nuclear Information System (INIS)

    Gillberg-Wickman, M.; Oestergren, I.

    1980-01-01

    The contamination of strontium-90 in Swedish milk during 1978 is practically the same as in 1977. The country-wide mean ratio of strontium-90 to calcium in milk is 0.12 Bq 90 Sr(gCa) -1 , based on monthly determinations of samples obtained from 8 dairy plants situated throughout the country. (author)

  4. Initial isotopic geochemistry ({delta} 18 O, {delta} D) of fluids from wells of the Los Humeros, Pue., geothermal field; Geoquimica isotopica ({delta} 18 O, {delta} D) inicial de fluidos de pozos del campo geotermico de Los Humeros, Pue.

    Energy Technology Data Exchange (ETDEWEB)

    Barragan Reyes, Rosa Maria; Arellano Gomez, Victor Manuel [Instituto de Investigaciones Electricas, Gerencia de Geotermia, Cuernavaca, Morelos (Mexico)]. E-mail: rmb@iie.org.mx; Ramirez Montes, Miguel; Tovar Aguado, Rigoberto [Comision Federal de Electricidad, Gerencia de Proyectos Geotermoelectricos, Morelia, Michoacan (Mexico)

    2010-01-15

    Isotopic data ({delta} 18 O, {delta} D) from fluids from production wells at the Los Humeros, Pue., geothermal field were analyzed to investigate the possible origin of these fluids and the dominant processes of the reservoir at its initial state. According to pre-exploitation data, it is suggested the Los Humeros reservoir fluids are made of a mixture of meteoric water of very light isotopic composition (paleo-fluids) and andesitic water. The relationship {delta} D vs {delta} 18 O from pre-exploitation data indicates the produced fluids are composed of a mixture of (at least) two fluids with distinct isotopic compositions. At the more enriched end of the mixing relationship are the isotopic compositions of the wells H-23 and H-18 (located in the southern area of the field), while the lighter fluids were found in well H-16 (originally) and then in well H-16 (repaired). It was found that the liquid phases of deep wells are more enriched in {delta} 18 O while the shallow wells present lower values, suggesting a convection process at the initial state. Based on this isotopic profile, it is considered that even the production depths of the wells H-1, H-12 and H-16 (repaired) are just about the same, but their respective isotopic compositions are quite different. The {delta} 18 O value for well H-16 (repaired) seems to be that of condensate steam, while the corresponding values for wells H-1 and H-12 fall within the value interval of the deep wells (H-23). This suggests wells H-1 and H-12 are collecting very deep fluids enriched in {delta} 18 O. These results could be useful in creating a conceptual model of the reservoir. [Spanish] Se analizaron datos isotopicos ({delta}18 O, {delta}D) de los fluidos de pozos productores del campo geotermico de Los Humeros, Pue., para investigar el posible origen de los fluidos asi como los procesos dominantes del yacimiento en su estado inicial. De acuerdo con datos previos a la explotacion, se plantea que los fluidos del yacimiento

  5. Methane clumped isotopes: Progress and potential for a new isotopic tracer

    Energy Technology Data Exchange (ETDEWEB)

    Douglas, Peter M. J.; Stolper, Daniel A.; Eiler, John M.; Sessions, Alex L.; Lawson, Michael; Shuai, Yanhua; Bishop, Andrew; Podlaha, Olaf G.; Ferreira, Alexandre A.; Santos Neto, Eugenio V.; Niemann, Martin; Steen, Arne S.; Huang, Ling; Chimiak, Laura; Valentine, David L.; Fiebig, Jens; Luhmann, Andrew J.; Seyfried, William E.; Etiope, Giuseppe; Schoell, Martin; Inskeep, William P.; Moran, James J.; Kitchen, Nami

    2017-11-01

    The isotopic composition of methane is of longstanding geochemical interest, with important implications for understanding hydrocarbon systems, atmospheric greenhouse gas concentrations, the global carbon cycle, and life in extreme environments. Recent analytical developments focusing on multiply substituted isotopologues (‘clumped isotopes’) are opening a potentially valuable new window into methane geochemistry. When methane forms in internal isotopic equilibrium, clumped isotopes can provide a direct record of formation temperature, making this property particularly valuable for identifying different methane origins. However, it has also become clear that in certain settings methane clumped isotope measurements record kinetic rather than equilibrium isotope effects. Here we present a substantially expanded dataset of methane clumped isotope analyses, and provide a synthesis of the current interpretive framework for this parameter. We review different processes affecting methane clumped isotope compositions, describe the relationships between conventional isotope and clumped isotope data, and summarize the types of information that this measurement can provide in different Earth and planetary environments.

  6. Rubidium-strontium isotoppe study of Muruntan deposit. 1.Ore vien dating by isochrone technique

    International Nuclear Information System (INIS)

    Kostitsyn, Yu.A.

    1993-01-01

    Hydrothermal viens of Muruntau gold-ore deposit (Central Kyzylkum) have been studies by the isochrone technique. The ages obtained for the quartz-tourmaline (257+13 Ma), quartz-arsenopyrite (230.3+-3.5 Ma) and quartz-adularia (219.4+-4.2 Ma) hydrothermal viens reflect the different stages of the deposit evolution: gold-ore and gold-silver one. Strontium isotope analysis reveals that the matter of hydrothermal viens is originated from the surrounding black schists

  7. Fundamental studies in isotope chemistry. Progress report, 1 August 1981-1 August 1982

    International Nuclear Information System (INIS)

    Bigeleisen, J.

    1982-01-01

    This research program is concerned with isotope chemistry and its applications. A summary of isotope separation activities during the past 5 years is included. Isotope effects are used as probes for chemical reactions, geochemistry, meteorology, and molecular biology, and this report also summarizes progress made in this area

  8. Strontium-90 measurements in Switzerland

    International Nuclear Information System (INIS)

    Friedli, C.; Geering, J.J.; Lerch, P.

    1988-01-01

    Strontium-90 contamination in Switzerland has been measured since the sixties. The determination of 90 Sr in human vertebrae, milk-teeth, milk and wine have shown a maximum activity between 1964 and 1966. Since 1976, the survey has been extended to the food chain. After the Chernobyl accident, the measurements indicated a significative 90 Sr contamination in the Tessin and the north-east of Switzerland. The partition of 90 Sr in wheat has been determined and transfer factors are given for the milk - cheese - whey chain

  9. Rare earth element and strontium isotopic study of seamount-type limestones in Mesozoic accretionary complex of Southern Chichibu Terrane, central Japan. Implication for incorporation process of seawater REE into limestones

    International Nuclear Information System (INIS)

    Tanaka, Kazuya; Miura, Noriko; Asahara, Yoshihiro; Kawabe, Iwao

    2003-01-01

    Ishimaki and Tahara limestones occur as exotic blocks juxtaposed in the Mesozoic (Jurassic) accretionary complex of Southern Chichibu Terrane in eastern Aichi Prefecture, central Japan. They are supposed to be of the seamount-type limestone, since they have no terrigenous materials and are intimately associated with greenstones. REE (rare earth elements) and Sr isotopic studies for the limestones have been made in order to know their geochemical characteristics, ages and origins. Their 87 Sr/ 86 Sr ratios, when referred to the seawater 87 Sr/ 86 Sr curve and relevant geological data, suggest that Ishimaki and Tahara limestones are the late Permian and the Carboniferous to the Early Permian, respectively. Two greenstone fragments found inside the Ishimaki limestone block and one greenstone sample associated with Tahara limestone block, resemble the Hawaiian alkali basalt in the their REE and Y patterns. This is supporting the idea that the limestone blocks may be parts of reef limestones on ancient volcanic seamounts. All the limestone samples, except three unusual Tahara ones, show seawater REE and Y signatures in their chondrite-normalized patterns. Their REE/Ca ratios, however, are 10 2 -10 4 times as high as those ratios of modern biogenic carbonates like corals and the seawater. Accordingly, seawater REE and Y were incorporated into the limestones, when originally biogenic carbonates transformed into inorganic calcite and its secondary growths occurred in diagenesis in contact with sufficient seawater. This view is favored by the reported REE partition experiment between calcite overgrowths and seawater solution. The seawater Ce anomaly as a function of water depth in the modern ocean is a key to infer the water depth of the REE and Y incorporation. The Ce anomalies given by log (Ce/Ce*) for about a half of Ishimaki samples and most of Tahara ones are between -0.5 and -0.2, which are compatible with the shallow water origin. Another half of Ishimaki samples

  10. petrography, compositional characteristics and stable isotope ...

    African Journals Online (AJOL)

    PROF EKWUEME

    Subsurface samples of the predominantly carbonate Ewekoro Formation, obtained from Ibese core hole within the Dahomey basin were used in this study. Investigations entail petrographic, elemental composition as well as stable isotopes (carbon and oxygen) geochemistry in order to deduce the different microfacies and ...

  11. Organic geochemistry of Czech amber

    Czech Academy of Sciences Publication Activity Database

    Havelcová, Martina; Sýkorová, Ivana; Mach, K.; Dvořák, Z.

    2015-01-01

    Roč. 11, č. 1 (2015), s. 146 ISSN 1336-7242. [Zjazd chemikov /67./. 07.09.2015-11.09.2015, Horný Smokovec] R&D Projects: GA ČR(CZ) GA13-18482S Institutional research plan: CEZ:AV0Z30460519 Keywords : fossil resin * amber * resinite Subject RIV: DD - Geochemistry

  12. Molecular environmental geochemistry

    Science.gov (United States)

    O'Day, Peggy A.

    1999-05-01

    The chemistry, mobility, and bioavailability of contaminant species in the natural environment are controlled by reactions that occur in and among solid, aqueous, and gas phases. These reactions are varied and complex, involving changes in chemical form and mass transfer among inorganic, organic, and biochemical species. The field of molecular environmental geochemistry seeks to apply spectroscopic and microscopic probes to the mechanistic understanding of environmentally relevant chemical processes, particularly those involving contaminants and Earth materials. In general, empirical geochemical models have been shown to lack uniqueness and adequate predictive capability, even in relatively simple systems. Molecular geochemical tools, when coupled with macroscopic measurements, can provide the level of chemical detail required for the credible extrapolation of contaminant reactivity and bioavailability over ranges of temperature, pressure, and composition. This review focuses on recent advances in the understanding of molecular chemistry and reaction mechanisms at mineral surfaces and mineral-fluid interfaces spurred by the application of new spectroscopies and microscopies. These methods, such as synchrotron X-ray absorption and scattering techniques, vibrational and resonance spectroscopies, and scanning probe microscopies, provide direct chemical information that can elucidate molecular mechanisms, including element speciation, ligand coordination and oxidation state, structural arrangement and crystallinity on different scales, and physical morphology and topography of surfaces. Nonvacuum techniques that allow examination of reactions in situ (i.e., with water or fluids present) and in real time provide direct links between molecular structure and reactivity and measurements of kinetic rates or thermodynamic properties. Applications of these diverse probes to laboratory model systems have provided fundamental insight into inorganic and organic reactions at

  13. Strontium metabolism and mechanism of interaction with mineralized tissues

    International Nuclear Information System (INIS)

    Wadkins, C.L.; Fu Peng, C

    1981-01-01

    This paper examines the administration of strontium to birds and mammals which results in limited incorporation into skeletal tissue, depressed intestinal calcium absorption, and development of rachitic bone lesions. Comparison of radiostrontium and radiocalcium incorporation by intact animals reveals discrimination against strontium in favor of calcium. Comparison of the Sr 85 - Ca 2+ and Ca 45 - Ca 2+ exchange reveals discrimination against strontium in favor of calcium. Thus, this system manifests product specificity, strontium inhibition, strontium exchange, and discrimination observed with intact animals

  14. The origin of an oceanic plateau: Isotope geochemistry (Sr, Nd, Pb and Hf) of volcanic rocks from IODP Site U1347 and ODP Site 1213 (Hf data) on the Shatsky Rise (Northwest Pacific)

    Science.gov (United States)

    Heydolph, K.; Geldmacher, J.; Hoernle, K.

    2011-12-01

    K.HEYDOLPH1*, J.GELDMACHER2, 1 ,K.HOERNLE1 1IFM-GEOMAR, Wischhofstr. 1-3. D-24148 Kiel, Germany, (*correspondence: kheydolph@ifm-geomar.de) 2 Integrated Ocean Drilling Program, Texas A&M University, 1000 Discovery Drive, College Station, Texas 77845-9547 (geldmacher@iodp.tamu.edu) The submarine Shatsky Rise plateau, a unique large igneous province (LIP) in the northwest Pacific Ocean ca. 1500 km east of Japan, is the only large intraoceanic plateau, which formed during the Late Jurassic to Early Cretaceous at a time period with numerous reversals of the Earth's magnetic field. These magnetic reversals combined with bathymetric data allow a detailed reconstruction of the tectonic history. Accordingly the three main volcanic edifices Tamu, Ori and Shirshov massifs formed by massive volcanism during a short time span along a southwest - northeast trending, rapidly spreading triple junction. Therefore, the magnetic and bathymetric data suggest that the Shatsky Rise formed through the interaction of a mantle plume head with a ridge [1, 2]. We present new Sr, Nd and Pb (double spike) and for the first time Hf isotope data from volcanic rocks of relatively fresh basaltic lava flows from recent IODP Exp. 324 Site U1347 and ODP Leg 198 Site 1213 (Hf data) both located on Tamu massif the southernmost (oldest) volcanic edifice of Shtasky Rise. Initial 176Hf/177Hf and 143Nd/144Nd isotopic compositions are fairly uniform throughout the entire holes ranging between 0.283076 to 0.283100 and 0.512903 to 0.512981 respectively, showing neither distinct MORB nor intraplate (plume) affinity. Relatively unradiogenic 87Sr/86Sr data ranging from 0.70276 to 0.70296 mostly overlaps with Pacific MORB like values. In a Nd vs Hf isotope plot they form a tight cluster at the edge of the Pacific MORB field below the present-day Hf-Nd mantle array. Although initial Pb double spike 206Pb/204Pb and 208Pb/204Pb isotopic compositions for Site U1347 range from 18.13 to 18.46 and 37.71 to 37

  15. Cold seeps in Monterey Bay, California: Geochemistry of pore waters and relationship to benthic foraminiferal calcite

    Energy Technology Data Exchange (ETDEWEB)

    Gieskes, Joris, E-mail: jgieskes@ucsd.edu [Scripps Institution of Oceanography, IOD-0208, 9500 Gilman Drive, La Jolla, CA 92093-0208 (United States); Rathburn, Anthony E. [Scripps Institution of Oceanography, IOD-0208, 9500 Gilman Drive, La Jolla, CA 92093-0208 (United States)] [Indiana State University, Department of Earth and Environmental Systems, Terre Haute, IN 47809 (United States); Martin, Jonathan B. [University of Florida, Department of Geological Sciences, Gainesville, FL 32611-2120 (United States); Perez, M. Elena [Indiana State University, Department of Earth and Environmental Systems, Terre Haute, IN 47809 (United States)] [The Natural History Museum, Department of Palaeontology, Cromwell Road, London SW7 5BD (United Kingdom); Mahn, Chris [Scripps Institution of Oceanography, IOD-0208, 9500 Gilman Drive, La Jolla, CA 92093-0208 (United States); Bernhard, Joan M. [Woods Hole Oceanographic Institution, Geology and Geophysics Department, MS52, Woods Hole, MA 02543 (United States); Day, Shelley [University of Florida, Department of Geological Sciences, Gainesville, FL 32611-2120 (United States)

    2011-05-15

    Highlights: > We describe the geochemistry of pore waters in the Clam Flats area of Monterey Bay. > The geochemical data are compared with the {delta}{sup 13}C chemistry of benthic foraminifera. > Living foraminifera indicate little effects of pore water low {delta}{sup 13}C (DIC) in the clam bed. > This phenomenon and its implications are discussed in detail. > Implications with regards to paleo-methane seepage are discussed. - Abstract: An extensive geochemical and biogeochemical examination of CH{sub 4} seeps in the Clam Flats area of Monterey Bay provides insight into the character of relationships between seep geochemistry and benthic foraminiferal geochemistry. The area is characterized by sulfide-rich fluids. Sulfide increases are associated with large increases in alkalinity, as well as small decreases in dissolved Ca and Mg. In addition, only small increases in NH{sub 4} are observed, but values of {delta}{sup 13}C of dissolved inorganic C are as low as -60 per mille at shallow depths (<3 cm). These observations indicate that all these processes are related to the bacterial oxidation of CH{sub 4}, which is transported upward by slow seepage of pore fluids. The geochemistry of the pore fluids should be relevant to the geochemistry of the carbonate tests of living and dead foraminifera. However, a profound disequilibrium of approximately an order of magnitude occurs between the {delta}{sup 13}C values of stained (cytoplasm-containing) foraminiferal carbonate and the C isotope values of ambient pore water dissolved inorganic C. Reasons are unclear for this isotopic disequilibrium, but have important implications for interpretations of foraminiferal carbonate as a paleoenvironmental proxy. Much fine scale work is needed to fully understand the relationships between the biogeochemistry of benthic foraminifera and the geochemistry of the pore waters where they live.

  16. Cold seeps in Monterey Bay, California: Geochemistry of pore waters and relationship to benthic foraminiferal calcite

    International Nuclear Information System (INIS)

    Gieskes, Joris; Rathburn, Anthony E.; Martin, Jonathan B.; Perez, M. Elena; Mahn, Chris; Bernhard, Joan M.; Day, Shelley

    2011-01-01

    Highlights: → We describe the geochemistry of pore waters in the Clam Flats area of Monterey Bay. → The geochemical data are compared with the δ 13 C chemistry of benthic foraminifera. → Living foraminifera indicate little effects of pore water low δ 13 C (DIC) in the clam bed. → This phenomenon and its implications are discussed in detail. → Implications with regards to paleo-methane seepage are discussed. - Abstract: An extensive geochemical and biogeochemical examination of CH 4 seeps in the Clam Flats area of Monterey Bay provides insight into the character of relationships between seep geochemistry and benthic foraminiferal geochemistry. The area is characterized by sulfide-rich fluids. Sulfide increases are associated with large increases in alkalinity, as well as small decreases in dissolved Ca and Mg. In addition, only small increases in NH 4 are observed, but values of δ 13 C of dissolved inorganic C are as low as -60 per mille at shallow depths ( 4 , which is transported upward by slow seepage of pore fluids. The geochemistry of the pore fluids should be relevant to the geochemistry of the carbonate tests of living and dead foraminifera. However, a profound disequilibrium of approximately an order of magnitude occurs between the δ 13 C values of stained (cytoplasm-containing) foraminiferal carbonate and the C isotope values of ambient pore water dissolved inorganic C. Reasons are unclear for this isotopic disequilibrium, but have important implications for interpretations of foraminiferal carbonate as a paleoenvironmental proxy. Much fine scale work is needed to fully understand the relationships between the biogeochemistry of benthic foraminifera and the geochemistry of the pore waters where they live.

  17. Kuwaiti dolocrete: petrology, geochemistry and groundwater origin

    Science.gov (United States)

    El-Sayed, M. I.; Fairchild, I. J.; Spiro, B.

    1991-09-01

    Near-surface sediments in southern Kuwait show extensive development of duricrusts. The host materials are siliciclastic sandstones of the post-Eocene Kuwait Group. Inland, the duricrusts are dominantly pedogenic calcrete (with some silcrete and gypcrete), whereas within 10-20 km of the coast, dolomite is the dominant duricrust mineral. Both these dolocretes and the inland calcretes display a similar maturation sequence in which carbonate-rich nodules develop and coalesce, carbonate progressively replacing and displacing detrital grains. The dolomite of the dolocretes forms mosaics of crystals typically 10-70 μm in size, varying from simple rhombs to spherulites. An intermediate morphology, named artichoke dolomite from its appearance in SEM, is particularly abundant. Authigenic palygorskite is associated with the dolomite. Dissolution of cores or zones within dolomite crystals has occurred. Calcite is present as sparry crystals (always post-dating dolomite) and is the expected precipitate from present-day soil and groundwaters. Chemical analyses of dolomite show highly negative values of δ13C (- to - 10.7‰ PDB) and δ18O varying from + 0.6 to + 3.3‰ PDB. The oxygen isotope values are interpreted as reflecting evaporation of a marine-based fluid. Manganese values of around 1000 ppm show that this fluid was reducing. Strontium data show variability reflecting mineral-fluid reactions. The general absence of metastable carbonates and presence of zoning in dolomite crystals suggests that meteoric dilution of seawater also occurred. Given that the duricrusts lack biogenic features, the light carbon isotope values are taken to indicate oxidation of seeping hydrocarbons. The dolocretes are interpreted as groundwater precipitates near the water table of a brackish water body formed at a time of higher relative sea level than today.

  18. Fixation of Radioactive Strontium in Soil

    DEFF Research Database (Denmark)

    Gregers-Hansen, Birte

    1964-01-01

    of the other long-lived fission products. Much work2–5 has, therefore, been concerned with the possibility of bringing down the strontium-90 uptake by plants through ploughing or through the addition of lime or fertilizer to the soil. Another factor, the effect of ageing on the availability of strontium, has...... been considered6,7. In general, these methods appear to be of little practical value, except for deep ploughing and the liming of acid soils, both of which will reduce the strontium uptake by a factor of 3–4....

  19. Ceria and strontium titanate based electrodes

    DEFF Research Database (Denmark)

    2010-01-01

    A ceramic anode structure obtainable by a process comprising the steps of: (a) providing a slurry by dispersing a powder of an electronically conductive phase and by adding a binder to the dispersion, in which said powder is selected from the group consisting of niobium-doped strontium titanate......, vanadium-doped strontium titanate, tantalum-doped strontium titanate, and mixtures thereof, (b) sintering the slurry of step (a), (c) providing a precursor solution of ceria, said solution containing a solvent and a surfactant, (d) impregnating the resulting sintered structure of step (b...

  20. Strontium clusters: electronic and geometry shell effects

    DEFF Research Database (Denmark)

    Lyalin, Andrey G.; Solov'yov, Ilia; Solov'yov, Andrey V.

    2008-01-01

    charged strontium clusters consisting of up to 14 atoms, average bonding distances, electronic shell closures, binding energies per atom, and spectra of the density of electronic states (DOS). It is demonstrated that the size-evolution of structural and electronic properties of strontium clusters...... is governed by an interplay of the electronic and geometry shell closures. Influence of the electronic shell effects on structural rearrangements can lead to violation of the icosahedral growth motif of strontium clusters. It is shown that the excessive charge essentially affects the optimized geometry...

  1. Sorption isolation of strontium from seawater

    International Nuclear Information System (INIS)

    Avramenko, V.A.; Zheleznov, V.V.; Kaplun, E.V.; Sokol'nitskaya, T.A.; Yukhkam, A.A.

    2001-01-01

    Sorption isolation of strontium from seawater is considered and prospects of use of selective adsorbents for purification of seawater or liquid radioactive wastes mixed with seawater from 90 Sr are discussed. Comparative analysis of sorptive properties of adsorbents of different nature is done. It is shown that sorption-reagent materials developed by authors can to afford effective separation of 90 Sr from seawater. Possible mechanism of strontium sorption by these adsorbents is considered. The prospect of their use for purification of liquid radioactive wastes from strontium is shown [ru

  2. Optical lattice clock with Strontium atoms; Horloge a reseau optique a atomes de strontium

    Energy Technology Data Exchange (ETDEWEB)

    Baillard, X

    2008-01-15

    This thesis presents the latest achievements regarding the optical lattice clock with Strontium atoms developed at LNE-SYRTE. After a review of the different types of optical clocks that are currently under development, we stress on the concept of optical lattice clock which was first imagined for Sr{sup 87} using the {sup 1}S{sub 0} {yields} {sup 3}P{sub 0} transition. We exhibit the features of this atom, in particular the concept of magic wavelength for the trap, and the achievable performances for this kind of clock. The second part presents the experimental aspects, insisting particularly on the ultra-stable laser used for the interrogation of the atoms which is a central part of the experiment. Among the latest improvements, an optical pumping phase and an interrogation phase using a magnetic field have been added in order to refine the evaluation of the Zeeman effect. Finally, the last part presents the experimental results. The last evaluation of the clock using Sr{sup 87} atoms allowed us to reach a frequency accuracy of 2.6*10{sup -15} and a measurement in agreement with the one made at JILA (Tokyo university) at the 10{sup -15} level. On another hand, thanks to recent theoretical proposals, we made a measurement using the bosonic isotope Sr{sup 88} by adapting the experimental setup. This measurement represents the first evaluation for this type of clock, with a frequency accuracy of 7*10{sup -14}. (author)

  3. Petrogenesis and geodynamic implications of Ediacaran highly fractionated A-type granitoids in the north Arabian-Nubian Shield (Egypt): Constraints from whole-rock geochemistry and Sr-Nd isotopes

    Science.gov (United States)

    Sami, Mabrouk; Ntaflos, Theodoros; Farahat, Esam S.; Mohamed, Haroun A.; Hauzenberger, Christoph; Ahmed, Awaad F.

    2018-04-01

    Mineral chemistry, whole-rock geochemical and Sr-Nd isotopic data are reported for the Abu-Diab granitoids in the northern Arabian-Nubian Shield (ANS) of Egypt, to investigate their petrogenesis and geodynamic significance. Gabal Abu-Diab constitute a multiphase pluton, consisting largely of two-mica granites (TMGs) enclosing microgranular enclaves and intruded by garnet bearing muscovite granites (GMGs) and muscovite granites (MGs). The granitoids are weakly peraluminous (A/CNK = 1.01-1.12) and show high SiO2 (>72.9 wt%) and alkali (K2O + Na2O = 8.60-9.13) contents. The geochemical features show that they are post-collisional and highly fractionated A-type granitoids. Compared to their host TMGs, the microgranular enclaves are strongly peraluminous (A/CNK = 1.18-1.24) with lower SiO2 and higher abundances of trace elements. The TMGs are depleted in Ba, Nb, P and Ti and are enriched in LREEs relative to HREEs with weakly negative Eu anomalies (Eu/Eu* = 0.45-0.64). In contrast, the GMGs and MGs are extremely depleted in Ba, Sr and Ti and have tetrad-type REE patterns (TE1-3 = 1.1-1.3) with strongly pronounced negative Eu anomalies (Eu/Eu* = 0.03-0.26), similar to rare metals bearing granites. The Ediacaran (585 ± 24 Ma) TMGs, are characterized by restricted and relatively low initial 87Sr/86Sr ratios (0.70337-0.70382) that suggests their derivation from a depleted mantle source, with little contamination from the older continental crust. In contrast, the GMGs and MGs have extremely high 87Rb/86Sr and 87Sr/86Sr ratios that reflect the disturbance of the Rb-Sr isotopic system and may give an indication for magmatic-fluid interaction. However, all the granitoids display positive εNd(t) (4.41-6.57) and depleted mantle model ages TDM2 between 777 and 956 Ma, which indicate their derivation from a Neoproterozoic juvenile magma sources and preclude the occurrence of pre-Neoproterozoic crustal rocks in the ANS. The microgranular enclaves represent globules of hot mafic

  4. 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

    Strontium and carbon isotopes of marine carbonates are routinely applied for chemostratigraphic cross correlations of time-equivalent sedimentary sequences and for calibration of the compositional evolution of seawater throughout Earth's history, mainly for the purpose of reconstructing ancient c...

  5. Geochronology, geochemistry, and Sr-Nd-Pb-Hf isotopes of the Zhunsujihua granitoid intrusions associated with the molybdenum deposit, northern Inner Mongolia, China: implications for petrogenesis and tectonic setting

    Science.gov (United States)

    Zhang, Xiaojun; Lentz, David R.; Yao, Chunliang; Liu, Rui; Yang, Zhen; Mei, Yanxiong; Fan, Xianwang; Huang, Fei; Qin, Ying; Zhang, Kun; Zhang, Zhenfei

    2018-03-01

    The Zhunsujihua porphyry molybdenum deposit, located in northern Inner Mongolia of China that belongs to Central-Asian Orogenic Belt (CAOB), is the only Mo deposit formed in the late Carboniferous in this area so far. Its mineralization is mainly restricted to the Zhunsujihua granitoid intrusions, which are composed of the main granodiorite (GD) and crosscutting, virtually coeval minor syn-ore leucogranite (LG) and diorite porphyry (DP) dykes. LA-ICP-MS zircon U-Pb dating yields crystallization ages of 300.0 ± 2.0, 299.3 ± 2.0, and 299.0 ± 2.6 Ma for the GD, LG, and DP, respectively. The major and trace element lithogeochemical data show that the GD and LG are metaluminous to weakly peraluminous, high-K calc-alkaline series with I-type granite characteristics, strongly oxidized, with low concentrations of Ba, Nb, Sr, P, and Ti and elevated K and Rb contents, indicating typical arc magmatic features. The LG is a product derived by extensive fractional crystallization of a parental magma similar to the GD as evident from the lower Eu/Eu*, Nb/Ta, Zr/Hf, and T Zr. The moderately altered DP exhibits high concentrations of K, Rb, Cs, LREE, Y, and low Sr/Y, with a positive ɛ Nd (300 Ma), which indicates a mantle or juvenile source associated with an arc setting. The Sr-Nd-Hf isotope data show low I Sr (0.70406-0.7