Sample records for accurate sr isotope

  1. Development of an on-line flow injection Sr/matrix separation method for accurate, high-throughput determination of Sr isotope ratios by multiple collector-inductively coupled plasma-mass spectrometry.

    PubMed

    Galler, Patrick; Limbeck, Andreas; Boulyga, Sergei F; Stingeder, Gerhard; Hirata, Takafumi; Prohaska, Thomas

    2007-07-01

    This work introduces a newly developed on-line flow injection (FI) Sr/Rb separation method as an alternative to the common, manual Sr/matrix batch separation procedure, since total analysis time is often limited by sample preparation despite the fast rate of data acquisition possible by inductively coupled plasma-mass spectrometers (ICPMS). Separation columns containing approximately 100 muL of Sr-specific resin were used for on-line FI Sr/matrix separation with subsequent determination of (87)Sr/(86)Sr isotope ratios by multiple collector ICPMS. The occurrence of memory effects exhibited by the Sr-specific resin, a major restriction to the repetitive use of this costly material, could successfully be overcome. The method was fully validated by means of certified reference materials. A set of two biological and six geological Sr- and Rb-bearing samples was successfully characterized for its (87)Sr/(86)Sr isotope ratios with precisions of 0.01-0.04% 2 RSD (n = 5-10). Based on our measurements we suggest (87)Sr/(86)Sr isotope ratios of 0.713 15 +/- 0.000 16 (2 SD) and 0.709 31 +/- 0.000 06 (2 SD) for the NIST SRM 1400 bone ash and the NIST SRM 1486 bone meal, respectively. Measured (87)Sr/(86)Sr isotope ratios for five basalt samples are in excellent agreement with published data with deviations from the published value ranging from 0 to 0.03%. A mica sample with a Rb/Sr ratio of approximately 1 was successfully characterized for its (87)Sr/(86)Sr isotope signature to be 0.718 24 +/- 0.000 29 (2 SD) by the proposed method. Synthetic samples with Rb/Sr ratios of up to 10/1 could successfully be measured without significant interferences on mass 87, which would otherwise bias the accuracy and uncertainty of the obtained data.

  2. In-situ Sr isotopic measurement of scheelite using fs-LA-MC-ICPMS

    NASA Astrophysics Data System (ADS)

    Li, Chao; Zhou, Limin; Zhao, Zheng; Zhang, Zhiyuan; Zhao, Hong; Li, Xinwei; Qu, Wenjun

    2018-07-01

    Scheelite is one of the main ore minerals in tungsten deposits, and Sr isotopic compositions of scheelite can be used to examine the petrogenesis of igneous rocks and fluid metasomatism in mineralization processes. Both thermal ionization mass spectrometer (TIMS) and femsecond laser ablation multi-collector inductively coupled plasma mass spectrometer (fs-LA-MC-ICP-MS) have been applied to analyze Sr isotopic compositions in scheelite. Here we describe a LA-MC-ICP-MS technique which can obtain in-situ, accurate, high precision 87Sr/86Sr ratios from 20 to 50 μm scheelite in line mode without requiring time-consuming mineral separation and pre-chemical procedures. We found that Ca dimers and Ca argides do not detectably affect the obtained 87Sr/86Sr ratios, and the adopted protocol overcomes interferences from Kr+, Rb+, Er2+ and Yb2+. The results of three MPI-DING reference glasses (KL2-G, ML3B-G and StHs6/80-G) are consistent with the recommended values. Here we show that the values of 87Sr/86Sr are relatively homogeneous for two scheelites from quartz veins, and are comparable to the values determined by a traditional solution method. Hence, these two scheelite samples have the potential to be reference materials for Sr isotopic determination by LA-MC-ICP-MS. To illustrate the utility of the technique, Sr isotopes of scheelites from three different types of tungsten deposits of South China are documented. The 87Sr/86Sr of scheelite from granite-related veinlet-disseminated and porphyry tungsten deposits varies systematically, showing a positive correlation between Sr content and 87Sr/86Sr ratios. These micrometer scale inhomogeneities could be explained by mixing of two components, reflecting intense fluid metasomatism during mineralization processes. High 87Sr/86Sr ratios were obtained for the scheelite samples from a quartz vein type tungsten deposit, indicating that the late stage ore-forming fluid was mainly derived from the surrounding strata. These examples

  3. Sr isotopic tracer study of the Samail ophiolite, Oman.

    USGS Publications Warehouse

    Lanphere, M.A.; Coleman, R.G.; Hopson, C.A.

    1981-01-01

    Rb and Sr concentrations and Sr-isotopic compositions were measured in 41 whole-rock samples and 12 mineral separates from units of the Samail ophiolite, including peridotite, gabbro, plagiogranite, diabase dykes, and gabbro and websterite dykes within the metamorphic peridotite. Ten samples of cumulate gabbro from the Wadir Kadir section and nine samples from the Wadi Khafifah section have 87Sr/86Sr ratios of 0.70314 + or - 0.00030 and 0.70306 + or - 0.00034, respectively. The dispersion in Sr- isotopic composition may reflect real heterogeneities in the magma source region. The average Sr-isotopic composition of cumulate gabbro falls in the range of isotopic compositions of modern MORB. The 87Sr/86Sr ratios of noncumulate gabbro, plagiogranite, and diabase dykes range 0.7034-0.7047, 0.7038-0.7046 and 0.7037- 0.7061, respectively. These higher 87Sr/86Sr ratios are due to alteration of initial magmatic compositions by hydrothermal exchange with sea-water. Mineral separates from dykes that cut harzburgite tectonite have Sr-isotopic compositions which agree with that of cumulate gabbro. These data indicate that the cumulate gabbro and the different dykes were derived from partial melting of source regions that had similar long-term histories and chemical compositions.-T.R.

  4. Rb-Sr and Sm-Nd Ages of Zagami DML and SR Isotopic Heterogeneity in Zagami

    NASA Technical Reports Server (NTRS)

    Nyquist, L.aurenceE.; Shih, C.-Y.; Reese, Y. D.

    2010-01-01

    Zagami contains lithologic heterogeneity suggesting that it did not form in a homogeneous, thick lava flow [1]. We have previously investigated the Sr and Nd isotopic systematics of Coarse-Grained (CG) and Fine-Grained (FG) lithologies described by [2]. Both appear to belong to Normal Zagami (NZ) [1,3], but their initial Sr-isotopic compositions differ [4,5]. Here we report new analyses of the Dark Mottled Lithology (DML, [3]) that show its age and initial Sr and Nd isotopic compositions to be identical within error limits with those of CG, but Sr initial isotopic compositions differ from those of FG.

  5. Precise determination of triple Sr isotopes (δ⁸⁷Sr and δ⁸⁸Sr) using MC-ICP-MS.

    PubMed

    Liu, Hou-Chun; You, Chen-Feng; Huang, Kuo-Fang; Chung, Chuan-Hsiung

    2012-01-15

    The non-traditional stable strontium (Sr) isotopes have received increasing attention recently as new geochemical tracers for studying Sr isotopic fractionation and source identification. This has been attributed to the advancement in multiple-collector inductively coupled plasma mass spectrometry (MC-ICP-MS), allows to determine precisely and simultaneously of the triple Sr isotopes. In this study, we applied a modified empirical external normalization (EEN) MC-ICPMS procedure for mass bias correction in Sr isotopic measurement using (92)Zr/(90)Zr. High-purity Zr Standard was spiked into sample solutions and the degree of fractionation was calculated off-line using an exponential law. The long-term external reproducibility for NIST SRM 987 δ(87)Sr and δ(88)Sr was better than 0.040‰ and 0.018‰ (2SD), respectively. The IAPSO standard seawater was used as a secondary standard to validate the analytical protocol and the absolute ratios measured were 0.709161±0.000018 for (87)Sr/(86)Sr, 0.177±0.021‰ for δ(87)Sr, and 0.370±0.026‰ for δ(88)Sr (2SD, n=7). These values are in good agreement with the literature data analyzed by thermal ionization mass spectrometry (TIMS) double spike technique. Rock standards, BHVO-2, BCR-2 and AGV-2 were also analyzed to validate the robustness of the methodology and showed identical results with literature data. Compared to previous (91)Zr/(90)Zr correction, we obtained improved results based on (92)Zr/(90)Zr, probably due to similar mass difference between (92)Zr/(90)Zr and measured Sr isotopes. The new analytical protocol presented in this study not only improves the analytical precision but also increases sample efficiency by omitting the use of the standard-sample bracketing (SSB) procedure. Copyright © 2011 Elsevier B.V. All rights reserved.

  6. Exploring the Middle Pleistocene Lake Suguta Sr-isotope Stratigraphic record

    NASA Astrophysics Data System (ADS)

    Vonhof, Hubert; Junginger, Annett; Agmon, Nadav; Trauth, Martin

    2017-04-01

    Several studies into the Quaternary stratigraphic record of the Sr-isotope composition of paleolake Turkana in the East African Rift System (EARS) show how variation of climate left a signal of changing lacustrine Sr isotope values. This Sr isotope signal was captured in the lacustrine fossil record of the Turkana Basin, and can be a useful chemostratigraphic tool (e.g. Joordens et al., 2011; van der Lubbe et al., submitted). Such lacustrine Sr-isotope changes are believed to be paced by orbital-forced insolation cyclicity, and interpreted to be the result of changing contribution of run-off from different sub-catchments of lake Turkana, as climate change shifted regional rainfall patterns. Here, we present a first set of data from a middle Pleistocene stratigraphical sequence in the Suguta Valley, South of the Turkana Basin in the EARS. This sequence spans a couple of sedimentological cycles that potentially represent precession-forced lake level variation. In this setting, the Sr-isotope data do not vary in phase with these sedimentological cycles, but demonstrate a long trend of Sr isotope change. This may suggest that the catchment configuration of the Suguta Valley in the Mid Pleistocene was less suitable to record precession-forced hydroclimate change in Lacustrine Sr isotope ratios. This may have implications for the Turkana Basin Sr isotope record as well, because the two basins are believed to have been hydrologically connected in the Middle Pleistocene. references: 1)Joordens, J.C.A. et al., 2011. An astronomically-tuned climate framework for hominins in the Turkana Basin. Earth and Planetary Science Letters 307, 1-8. 2)van der Lubbe et al., submitted. Gradual or abrupt? Changes in water source of Lake Turkana (Kenya) during the African Humid Period inferred from Sr isotope ratios

  7. Investigating human geographic origins using dual-isotope (87Sr/86Sr, δ18O) assignment approaches.

    PubMed

    Laffoon, Jason E; Sonnemann, Till F; Shafie, Termeh; Hofman, Corinne L; Brandes, Ulrik; Davies, Gareth R

    2017-01-01

    Substantial progress in the application of multiple isotope analyses has greatly improved the ability to identify nonlocal individuals amongst archaeological populations over the past decades. More recently the development of large scale models of spatial isotopic variation (isoscapes) has contributed to improved geographic assignments of human and animal origins. Persistent challenges remain, however, in the accurate identification of individual geographic origins from skeletal isotope data in studies of human (and animal) migration and provenance. In an attempt to develop and test more standardized and quantitative approaches to geographic assignment of individual origins using isotopic data two methods, combining 87Sr/86Sr and δ18O isoscapes, are examined for the Circum-Caribbean region: 1) an Interval approach using a defined range of fixed isotopic variation per location; and 2) a Likelihood assignment approach using univariate and bivariate probability density functions. These two methods are tested with enamel isotope data from a modern sample of known origin from Caracas, Venezuela and further explored with two archaeological samples of unknown origin recovered from Cuba and Trinidad. The results emphasize both the potential and limitation of the different approaches. Validation tests on the known origin sample exclude most areas of the Circum-Caribbean region and correctly highlight Caracas as a possible place of origin with both approaches. The positive validation results clearly demonstrate the overall efficacy of a dual-isotope approach to geoprovenance. The accuracy and precision of geographic assignments may be further improved by better understanding of the relationships between environmental and biological isotope variation; continued development and refinement of relevant isoscapes; and the eventual incorporation of a broader array of isotope proxy data.

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

    NASA Astrophysics Data System (ADS)

    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

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

    NASA Astrophysics Data System (ADS)

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

    2010-12-01

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

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

    PubMed

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

    2015-04-15

    Geographical origin and authenticity of food are topics of interest for both consumers and producers. Among the different indicators used for traceability studies, (87)Sr/(86)Sr isotopic ratio has provided excellent results. In this study, two analytical approaches for wine sample pre-treatment, microwave and low temperature mineralisation, were investigated to develop accurate and precise analytical method for (87)Sr/(86)Sr determination. The two procedures led to comparable results (paired t-test, with tisotopic values were compared with isotopic data coming from (i) soils of their territory of origin and (ii) wines obtained by same grape varieties cultivated in different districts. The obtained results have shown no significant variability among the different vintages of wines and a perfect agreement between the isotopic range of the soils and wines has been observed. Nevertheless, the investigated indicator was not enough powerful to discriminate between similar products. To this regard, it is worth to note that more soil samples as well as wines coming from different districts will be considered to obtain more trustworthy results. Copyright © 2014 Elsevier Ltd. All rights reserved.

  11. Sr isotopic composition of Afar volcanics and its implication for mantle evolution

    NASA Astrophysics Data System (ADS)

    Barberi, F.; Civetta, L.; Varet, J.

    1980-10-01

    Investigations of Rb-Sr systematics of basalts from the Afar depression (Ethiopia) indicate the presence of a heterogeneous mantle source region. The Sr isotopic compositions of the basalts from the Afar axial and transverse ranges identify source regions which are enriched in LIL elements and radiogenic Sr (axial ranges) and others which are relatively depleted (transverse ranges). Sr isotopic composition of basalts from the Red Sea, Gulf of Aden and Gulf of Tadjoura, which range from 0.70300 to 0.70340 are also reported and compared with the more radiogenic Afar region, which is characterized by 87Sr/ 86Sr ranging from 0.70328 to 0.70410. Available geochemical and isotopic data suggest that a relation exists between magma composition and the advancement of the rifting process through progressive lithosphere attenuation leading to continental break-up. However, the petrogenetic process is not simple and probably implies a vertically zoned mantle beneath the Afar region. Sr isotopic evidence suggests that the vertically zoned mantle is more radiogenic and enriched in LIL elements in its upper part.

  12. All-diode-laser cooling of Sr+ isotope ions for analytical applications

    NASA Astrophysics Data System (ADS)

    Jung, Kyunghun; Yamamoto, Kazuhiro; Yamamoto, Yuta; Miyabe, Masabumi; Wakaida, Ikuo; Hasegawa, Shuichi

    2017-06-01

    Trapping and cooling of Sr+ isotope ions by an all-diode-laser system has been demonstrated in order to develop a novel mass spectrometric technique in combination with ion trap-laser cooling. First, we constructed external cavity diode lasers and associated stabilization apparatus for laser cooling of Sr+ ions. The transition frequencies confirmed by optogalvanic spectroscopy enabled successful cooling of 88Sr+ ions. An image of two trapped ions has been captured by CCD camera. Minor isotopes, 84Sr+ and 86Sr+, were also cooled and trapped. From an analysis of the observed spectra of a string crystal of each isotope, the isotope shifts of the cooling transition (5s 2S1/2 → 5p 2P1/2) of Sr+ ions were determined to be +371(8) MHz for Δν84-88 and +169(8) MHz for Δν86-88. In the case of the repumping transition (4d 2D3/2 → 5p 2P1/2), Δν84-88 and Δν86-88 were measured to be -833(6) and -400(5) MHz, respectively. These values are in good agreement with previously reported values.

  13. Potential of Sr isotopic analysis in ceramic provenance studies: Characterisation of Chinese stonewares

    NASA Astrophysics Data System (ADS)

    Li, Bao-Ping; Zhao, Jian-Xin; Greig, Alan; Collerson, Kenneth D.; Zhuo, Zhen-Xi; Feng, Yue-Xin

    2005-11-01

    We compare the trace element and Sr isotopic compositions of stoneware bodies made in Yaozhou and Jizhou to characterise these Chinese archaeological ceramics and examine the potential of Sr isotopes in provenance studies. Element concentrations determined by ICP-MS achieve distinct characterisation for Jizhou samples due to their restricted variation, yet had limited success with Yaozhou wares because of their large variability. In contrast, 87Sr/86Sr ratios in Yaozhou samples have a very small variation and are all significantly lower than those of Jizhou samples, which show a large variation and cannot be well characterised with Sr isotopes. Geochemical interpretation reveals that 87Sr/86Sr ratios will have greater potential to characterise ceramics made of low Rb/Sr materials such as kaolin clay, yet will show larger variations in ceramics made of high Rb/Sr materials such as porcelain stone.

  14. Strontium isotope measurement of basaltic glasses by laser ablation multiple collector inductively coupled plasma mass spectrometry based on a linear relationship between analytical bias and Rb/Sr ratios.

    PubMed

    Zhang, Le; Ren, Zhong-Yuan; Wu, Ya-Dong; Li, Nan

    2018-01-30

    In situ strontium (Sr) isotope analysis of geological samples by laser ablation multiple collector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) provides useful information about magma mixing, crustal contamination and crystal residence time. Without chemical separation, during Sr isotope analysis with laser ablation, many kinds of interference ions (such as Rb + and Kr + ) are on the Sr isotope spectrum. Most previous in situ Sr isotope studies only focused on Sr-enriched minerals (e.g. plagioclase, calcite). Here we established a simple method for in situ Sr isotope analysis of basaltic glass with Rb/Sr ratio less than 0.14 by LA-MC-ICP-MS. Seven Faraday cups, on a Neptune Plus MC-ICP-MS instrument, were used to receive the signals on m/z 82, 83, 84, 85, 86, 87 and 88 simultaneously for the Sr isotope analysis of basaltic glass. The isobaric interference of 87 Rb was corrected by the peak stripping method. The instrumental mass fractionation of 87 Sr/ 86 Sr was corrected to 86 Sr/ 88 Sr = 0.1194 with an exponential law. Finally, the residual analytical biases of 87 Sr/ 86 Sr were corrected with a relationship between the deviation of 87 Sr/ 86 Sr from the reference values and the measured 87 Rb/ 86 Sr. The validity of the protocol present here was demonstrated by measuring the Sr isotopes of four basaltic glasses, a plagioclase crystal and a piece of modern coral. The measured 87 Sr/ 86 Sr ratios of all these samples agree within 100 ppm with the reference values. In addition, the Sr isotopes of olivine-hosted melt inclusions from the Emeishan large igneous province (LIP) were measured to show the application of our method to real geological samples. A simple but accurate approach for in situ Sr isotope measurement by LA-MC-ICP-MS has been established, which should greatly facilitate the wider application of in situ Sr isotope geochemistry, especially to volcanic rock studies. Copyright © 2017 John Wiley & Sons, Ltd.

  15. Tracing subduction zone fluid-rock interactions using trace element and Mg-Sr-Nd isotopes

    NASA Astrophysics Data System (ADS)

    Wang, Shui-Jiong; Teng, Fang-Zhen; Li, Shu-Guang; Zhang, Li-Fei; Du, Jin-Xue; He, Yong-Sheng; Niu, Yaoling

    2017-10-01

    Slab-derived fluids play a key role in mass transfer and elemental/isotopic exchanges in subduction zones. The exhumation of deeply subducted crust is achieved via a subduction channel where fluids from various sources are abundant, and thus the chemical/isotopic compositions of these rocks could have been modified by subduction-zone fluid-rock interactions. Here, we investigate the Mg isotopic systematics of eclogites from southwestern Tianshan, in conjunction with major/trace element and Sr-Nd isotopes, to characterize the source and nature of fluids and to decipher how fluid-rock interactions in subduction channel might influence the Mg isotopic systematics of exhumed eclogites. The eclogites have high LILEs (especially Ba) and Pb, high initial 87Sr/86Sr (up to 0.7117; higher than that of coeval seawater), and varying Ni and Co (mostly lower than those of oceanic basalts), suggesting that these eclogites have interacted with metamorphic fluids mainly released from subducted sediments, with minor contributions from altered oceanic crust or altered abyssal peridotites. The positive correlation between 87Sr/86Sr and Pb* (an index of Pb enrichment; Pb* = 2*PbN/[CeN + PrN]), and the decoupling relationships and bidirectional patterns in 87Sr/86Sr-Rb/Sr, Pb*-Rb/Sr and Pb*-Ba/Pb spaces imply the presence of two compositionally different components for the fluids: one enriched in LILEs, and the other enriched in Pb and 87Sr/86Sr. The systematically heavier Mg isotopic compositions (δ26Mg = - 0.37 to + 0.26) relative to oceanic basalts (- 0.25 ± 0.07) and the roughly negative correlation of δ26Mg with MgO for the southwestern Tianshan eclogites, cannot be explained by inheritance of Mg isotopic signatures from ancient seafloor alteration or prograde metamorphism. Instead, the signatures are most likely produced by fluid-rock interactions during the exhumation of eclogites. The high Rb/Sr and Ba/Pb but low Pb* eclogites generally have high bulk-rock δ26Mg values

  16. Additional Sr Isotopic Heterogeneity in Zagami Olivine-Rich Lithology

    NASA Technical Reports Server (NTRS)

    Misawa, K.; Niihara, T.; Shih, C.-Y; Reese, Y. D.; Nyquist, L. E.; Yoneda, S.; Yamashita, H.

    2012-01-01

    Prior isotopic analyses of Zagami have established differing initial Sr-87/Sr-86 (ISr) ratios of among Zagami lithologies, fine-grained (FG), coarse-grained (CG), and dark mottled lithologies (DML)]. The Zagami sample (KPM-NLH000057) newly allocated from the Kanagawa Prefectural Museum of Natural History contained DML and the Ol-rich lithology which included more ferroan olivines (Ol-rich: Fa(sub 97- 99) vs late-stage melt pockets: Fa(sub 90-97)]). We have combined mineralogy-petrology and Rb-Sr isotopic studies on the Kanagawa Zagami sample, which will provide additional clues to the genesis of enriched shergottites and to the evolution of Martian crust and mantle

  17. Asian dust input in the western Philippine Sea: Evidence from radiogenic Sr and Nd isotopes

    NASA Astrophysics Data System (ADS)

    Jiang, Fuqing; Frank, Martin; Li, Tiegang; Chen, Tian-Yu; Xu, Zhaokai; Li, Anchun

    2013-05-01

    The radiogenic strontium (Sr) and neodymium (Nd) isotope compositions of the detrital fraction of surface and subsurface sediments have been determined to trace sediment provenance and contributions from Asian dust off the east coast of Luzon Islands in the western Philippine Sea. The Sr and Nd isotope compositions have been very homogenous near the east coast of the Luzon Islands during the latest Quaternary yielding relatively least radiogenic Sr (87Sr/86Sr = 0.70453 to 0.70491) and more radiogenic Nd isotope compositions (ɛNd(0) = +5.3 to +5.5). These isotope compositions are similar to Luzon rocks and show that these sediments were mainly derived from the Luzon Islands. In contrast, the Sr and Nd isotope compositions of sediments on the Benham Rise and in the Philippine Basin are markedly different in that they are characterized by overall more variable and more radiogenic Sr isotope compositions (87Sr/86Sr = 0.70452 to 0.70723) and less radiogenic Nd isotope compositions (ɛNd(0) = -5.3 to +2.4). The Sr isotope composition in the Huatung Basin is intermediate between those of the east coast of Luzon and Benham Rise, but shows the least radiogenic Nd isotope compositions. The data are consistent with a two end-member mixing relationship between Luzon volcanic rocks and eolian dust from the Asian continent, which is characterized by highly radiogenic Sr and unradiogenic Nd isotope compositions. The results show that Asian continental dust contributes about 10-50% of the detrital fraction of the sediments on Benham Rise in the western Philippine Sea, which offers the potentials to reconstruct the climatic evolution of eastern Asia from these sediments and compare this information to the records from the central and northern Pacific.

  18. Transgenerational isotopic marking of carp Cyprinus carpio, L. using a 86Sr /84Sr double spike

    NASA Astrophysics Data System (ADS)

    Zitek, Andreas; Cervicek, Magdalena; Irrgeher, Johanna; Horsky, Monika; Kletzl, Manfred; Weismann, Thomas; Prohaska, Thomas

    2013-04-01

    Transgenerational isotopic marking has been recognized recently as an effective tool for mass marking and tracking of individual fish to their original source. Compared to other conventional marking techniques, transgenerational marking offers several advantages. Most importantly, it is possible to mark all offspring of one individual female without the necessity of handling eggs or larval fish. Furthermore it is possible to vary the concentrations of individual isotopes to obtain specific marks for individual female fish. An enriched isotopic spike solution is usually applied to gravid female spawners by injection into the body cavity for transgenerational marking. The isotope is then incorporated into the central otolith region of the offspring which is known to be built up by maternally derived material. Within this study transgenerational marking of a typical cyprinid fish species, Cyprinus carpio, L., was tested using a 86Sr /84Sr double spike. Buffered solutions with different isotopic composition and concentrations were administered to 4 female individuals by intraperitoneal injection 5 days before spawning, while one female was injected a blank solution. After spawning, otoliths (Lapilli) from juvenile fish were sampled at the age of about 5 months at fish sizes between 3 and 4 cm and analyzed for their isotopic composition by LA-ICPMS applying cross sectional line scans. Central otolith regions of the progeny showed a shift in the natural isotope ratios for the administered isotopes. Deconvolution of the blank corrected measurement data of the Sr isotopes was done to trace back the original spike ratio. The different spike ratios could be well distinguished reflecting the original composition of the spike solution. This study proved that it is possible to create batch-specific unique transgenerational marks in otolith cores by varying the concentrations of two naturally occurring Sr isotopes. This method has high potential to reduce the marking effort for

  19. Source area and seasonal variation of dissolved Sr isotope composition in rivers of the Amazon basin

    NASA Astrophysics Data System (ADS)

    Santos, Roberto V.; Sondag, Francis; Cochonneau, Gerard; Lagane, Christelle; Brunet, Pierre; Hattingh, Karina; Chaves, Jeane G. S.

    2014-05-01

    We present dissolved Sr isotope data collected over 8 years from three main river systems from the Amazon Basin: Beni-Madeira, Solimões, Amazon, and Negro. The data show large 87Sr/86Sr ratio variations that were correlated with the water discharge and geology of the source areas of the suspended sediments. The Beni-Madeira system displays a high average 87Sr/86Sr ratio and large 87Sr/86Sr fluctuations during the hydrological cycle. This large average value and fluctuations were related to the presence of Precambrian rocks and Ordovician sediments in the source area of the suspended sediment of the river. In contrast, the Solimões system displays a narrow range of Sr isotope ratio variations and an average value close to 0.709. This river drains mostly Phanerozoic rocks of northern Peru and Ecuador that are characterized by low Sr isotope ratios. Despite draining areas underlain by Precambrian rocks and having high 87Sr/86Sr ratios, such rivers as the Negro and Tapajós play a minor role in the total Sr budget of the Amazon Basin. The isotopic fluctuations in the Beni-Madeira River were observed to propagate downstream at least as far as Óbidos, in the Amazon River. This signal is characterized by an inverse relationship between the concentration of elemental Sr and its isotopic ratios. During the raining season there is an increase in Sr isotopic ratio accompanied by a decrease in elemental Sr concentration. During the dry season, the Sr isotopic ration decreases and the elemental Sr concentration increases.

  20. Determination of (87)Sr/(86)Sr and δ(88/86)Sr ratios in plant materials using MC-ICP-MS.

    PubMed

    Liu, Hou-Chun; Chung, Chuan-Hsiung; You, Chen-Feng; Chiang, Yi-Hsuan

    2016-01-01

    A protocol for highly accurate and precise determination of Sr isotope ratios in plant materials, (87)Sr/(86)Sr and δ (88/86)Sr, by multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) is presented in this study. An Eichrom Sr resin was used for matrix separation and an improved Zr empirical external normalization coupled with standard-sample bracketing method (Zr EEN-SSB) was applied to mass bias correction during Sr isotope MC-ICP-MS measurements. Potential influences of matrix elements, and polyatomic and isobaric interferences on the Sr isotopic determination were further evaluated using NIST SRM 987 Sr isotopic standard spiked with various amount of Ca, Mg, and Rb contents. Concentrations of Ca and Mg lower than 30 ng g(-1) or Rb < 2 ng g(-1) in 150 ng g(-1) Sr analyte were estimated to have only a minor effect on Sr isotope ratios determination. On the other hand, intensity differences between sample and standards (IntSample/IntStandards) represented a large δ (88/86)Sr deviation of <0.9 or >1.3, reflecting the significance of intensity bias attributed to different mass bias behavior. An apple leaf material, NIST SRM 1515, was adopted as the plant material for overall evaluation of sample digestion, matrix separation, and potential spectral interferences on the measurements of Sr isotope ratios. Our results suggest that the partially remaining organic compounds in the incomplete digestion would have a significant bias on the extraction chromatography procedure, resulting in sizable uncertainty in δ (88/86)Sr ratios. Thus, complete digestion of the organic-enriched materials is of great importance for efficiency assurance in matrix separation. Extraction chromatography works well for the total digested samples, where Ca, Mg, and Rb were efficiently removed. The obtained average (87)Sr/(86)Sr and δ (88/86)Sr values for the NIST SRM 1515 apple leaves are 0.71398 ± 0.00004 and 0.23 ± 0.03‰ (2SD, n = 10

  1. Sr Isotopes and human skeletal remains, improving a methodological approach in migration studies

    NASA Astrophysics Data System (ADS)

    Solis Pichardo, G.; Schaaf, P. E.; Hernandez, T.; Horn, P.; Manzanilla, L. R.

    2013-12-01

    Asserting mobility of ancient humans is a major issue for anthropologists. Sr isotopes are widely used in anthropological sciences to trace human migration histories from ancient burials. Sr in bone approximately reflects the isotopic composition of the geological region where the person lived before death; whereas the Sr isotopic system in tooth enamel is thought to remain as a closed system and thus conserves the isotope ratio acquired during childhood. A comparison of the 87Sr/86Sr ratios found in tooth enamel and in bone is performed to determine if the human skeletal remains belonged to a local or a migrant. Until now, tooth enamel was considered to be less sensitive to secondary Sr contamination due to its higher crystallinity and larger sizes of the biogenic apatites in comparison to that in bone and dentine. In the past, enamel as well as bone material was powdered, dissolved and analyzed by thermal ionization mass spectrometry (TIMS). In this contribution we show, however, that simple dissolution of enamel frequently yields erroneous results. Tooth enamel is often affected by secondary strontium contamination processes such as caries or diagenetic and environmental input, which can change the original isotopic composition. To avoid these problems we introduced a pre-treatment and three-step leaching procedure in enamel samples. Leaching is carried out with acetic acid of different concentrations, yielding two leachates and one residue of each sample. Frequently the 87Sr/86Sr results of the three leachates display different values confirming that secondary contamination did occur. Several examples from Teotihuacan, central Mexico demonstrate that enamel 87Sr/86Sr without leaching can show correct biogenic values, but there is also a considerable probability for these values to represent a mixture of original and secondary Sr without significance for migration reconstructions. Only the residue value is interpreted by us as the representative ratio for

  2. 87Sr/86Sr isotope ratio analysis by laser ablation MC-ICP-MS in scales, spines, and fin rays as a nonlethal alternative to otoliths for reconstructing fish life history

    USGS Publications Warehouse

    Willmes, Malte; Glessner, Justin J. G.; Carleton, Scott A.; Gerrity, Paul C.; Hobbs, James A.

    2016-01-01

    Strontium isotope ratios (87Sr/86Sr) in otoliths are a well-established tool to determine origins and movement patterns of fish. However, otolith extraction requires sacrificing fish, and when working with protected or endangered species, the use of nonlethal samples such as scales, spines, and fin rays is preferred. Unlike otoliths that are predominantly aragonite, these tissues are composed of biological apatite. Laser ablation multicollector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) analysis of biological apatite can induce significant interference on mass 87, causing inaccurate 87Sr/86Sr measurements. To quantify this interference, we applied LA-MC-ICP-MS to three marine samples (white seabass (Atractoscion nobilis) otolith; green sturgeon (Acipenser medirostris) pectoral fin ray; salmon shark (Lamna ditropis) tooth), and freshwater walleye (Sander vitreus) otoliths, scales, and spines). Instrument conditions that maximize signal intensity resulted in elevated 87Sr/86Sr isotope ratios in the bioapatite samples, related to a polyatomic interference (40Ca31P16O, 40Ar31P16O). Retuning instrument conditions to reduce oxide levels removed this interference, resulting in accurate 87Sr/86Sr ratios across all tissue samples. This method provides a novel, nonlethal alternative to otolith analysis to reconstruct fish life histories.

  3. Observation of Isotope Ratios (δ2H, δ18O, 87Sr/86Sr) of Tap Water in Urban Environments

    NASA Astrophysics Data System (ADS)

    Mancuso, C. J.; Tipple, B. J.; Ehleringer, J. R.

    2014-12-01

    Urban environments are centers for rapidly growing populations. In order to meet the culinary water needs of these areas, municipal water departments use water from multiple locations and/or sources, often piped differentially to different locations within a municipality. This practice creates isotopically distinct locations within an urban area and therefore provides insight to urban water management practices. In our study we selected urban locations in the Salt Lake Valley, UT (SLV) and San Francisco Bay Area, CA (SFB) where we hypothesized geographically distinct water isotopic ratio differences existed. Within the SLV, municipal waters come from the same mountainous region, but are derived from different geologically distinct watersheds. In contrast, SFB waters are derived from regionally distinct water sources. We hypothesized that the isotope ratios of tap waters would differ based upon known municipal sources. To test this, tap water samples were collected throughout the urban regions in SLV and SFB and analyzed for δ2H, δ18O and 87Sr/86Sr isotope ratios. Seasonal collections were also made to assess if isotope ratios differed throughout the year. Within SLV and SFB, different regions were characterized by distinct paired δ18O and 87Sr/86Sr values. These different realms also agreed with known differences in municipal water supplies within the general geographic region. Waters from different cities within Marin County showed isotopic differences, consistent with water derived from different local reservoirs. Seasonal variation was observed in paired δ18O and 87Sr/86Sr values of tap water for some locations within SLV and SFB, indicating management decisions to shift from one water source to another depending on demand and available resources. Our study revealed that the δ18O and 87Sr/86Sr values of tap waters in an urban region can exhibit significant differences despite close spatial proximity if districts differ in their use of local versus

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

    PubMed

    Derry, L A; Keto, L S; Jacobsen, S B; Knoll, A H; Swett, K

    1989-01-01

    We report initial 87Sr/86Sr values from an Upper Proterozoic carbonate succession from Svalbard and East Greenland. This succession, now tectonically separated into three sequences, is thick, relatively continuous, and well preserved. The relative ages of the samples from within the basin are well constrained by litho-, bio-, and chemostratigraphic techniques. The data from this study and related data from the literature are used to construct a curve of 87Sr/86Sr for Upper Proterozoic seawater. The new data reported in this study substantially improve the isotopic record of Sr in seawater for the period between 650 and 800 Ma. The data indicate that delta 87Sr values of seawater were variable but low (delta 87Sr approximately -500 to -250) between 900 and 650 Ma, and rose rapidly to approximately +30 by 600 Ma. The range of variation of delta 87Sr in seawater during the Riphean-Vendian exceeds the entire range of delta 87Sr in seawater during the Phanerozoic. While variation in the average isotopic composition of Sr delivered to the oceans by rivers can account for some of the observed range, changes in the ratio of submarine hydrothermal flux to river water (continental) flux are responsible for the large variation in seawater Sr isotopic composition. Changes in the continental flux of Sr to the oceans can be related to tectonic factors. Large changes in the hydrothermal flux to river water flux ratio indicated by the data could have significant consequences for the chemistry of the ocean-atmosphere system.

  5. Sr isotopic composition as a tracer of Ca sources in two forest ecosystems in Belgium.

    NASA Astrophysics Data System (ADS)

    Drouet, T.; Herbauts, J.; Demaiffe, D.

    2003-04-01

    The two main sources of Ca in forest ecosystem are the mineral weathering release and atmospheric inputs. We use the 87Sr/86Sr isotopic ratio (Sr is a proxy for Ca) to determine the Ca contribution from rain input in two forest ecosystems (beech stands) growing on soils formed from parent materials with distinct total Ca contents and contrasted isotopic ratios: Pleistocene loess in Central Belgium (leached brown soil) with present-day 87Sr/86Sr =0.72788 and Lower Devonian shales and sandstones in Ardennes (ochreous brown earth) with 87Sr/86Sr = 0.76913. The 87Sr/86Sr ratios and the Ca and Sr contents were measured in rainwater, vegetation (beech wood growth rings and leaves) and main soil horizons (total, labile and HCl 0.1 M soluble forms). The relative contributions of atmospheric input and soil mineral weathering to vegetation were calculated using mixing equations. Calculations based on the Sr isotope ratios of rainwater (endmember 1; 87Sr/86Sr close to seawater: 0.7090), labile soil fraction (endmember 2; 87Sr/86Sr: 0.71332 to 0.71785) and beech wood (mixing compartment) indicate that about 50 % (Central Belgium) to 35 % (Ardennes) of Ca uptake originate from atmospheric inputs. The choice of the appropriate 87Sr/86Sr ratio for the weathering endmember is however critical. The isotopic composition of the mineral source is theoretically determined by the mineralogical composition of the soil and the relative weatherability of the Sr-bearing minerals. Due to soil processes (weathering and clay illuviation), the distribution of minerals in both soil profiles is not homogeneous and varies from horizon to horizon. Which horizons are relevant and which kind of soil extract (labile soil fraction, acid soluble fraction, total soil,...) should be selected for isotopic measurement of weathering endmember, is therefore questionable. The different ways of estimation are discussed. Quantitative mineralogical reconstitutions of soil horizons and isotopic data indicate

  6. Sr-Nd-Hf isotopic fingerprinting of transatlantic dust derived from North Africa

    NASA Astrophysics Data System (ADS)

    Zhao, Wancang; Balsam, William; Williams, Earle; Long, Xiaoyong; Ji, Junfeng

    2018-03-01

    Long-range transport of African dust plays an important role in understanding dust-climate relationships including dust source areas, dust pathways and associated atmospheric and/or oceanic processes. Clay-sized Sr-Nd-Hf isotopic compositions can be used as geochemical fingerprints to constrain dust provenance and the pathways of long-range transported mineral dust. We investigated the clay-sized Sr-Nd-Hf isotopic composition of surface samples along four transects bordering the Sahara Desert. The transects are from Mali, Niger/Benin/Togo, Egypt and Morocco. Our results show that the Mali transect on the West African Craton (WAC) produces lower εNd (εNd-mean = -16.38) and εHf (εHf-mean = -9.59) values than the other three transects. The Egyptian transect exhibits the lowest 87Sr/86Sr ratios (87Sr/86Srmean = 0.709842), the highest εHf (εHf-mean = -0.34) and εNd values of the four transects. Comparison of the clay-sized Sr-Nd-Hf isotopic values from our North African samples to transatlantic African dust collected in Barbados demonstrates that the dust's provenance is primarily the western Sahel and Sahara as well as the central Sahel. Summer emission dust is derived mainly from the western Sahel and Sahara regions. The source of transatlantic dust in spring and autumn is more varied than in the summer and includes dust not only from western areas, but also south central areas. Comparison of the Sr-Nd-Hf isotopic fingerprints between the source and sink of transatlantic dust also suggests that a northwestward shift in dust source occurs from the winter, through the spring and into the summer. The isotopic data we develop here provide another tool for discriminating changes in dust archives resulting from paleoenvironmental evolution of source regions.

  7. New aragonite 87Sr/86Sr records of Mesozoic ammonoids and approach to the problem of N, O, C and Sr isotope cycles in the evolution of the Earth

    NASA Astrophysics Data System (ADS)

    Zakharov, Yuri D.; Dril, Sergei I.; Shigeta, Yasunari; Popov, Alexander M.; Baraboshkin, Eugenij Y.; Michailova, Irina A.; Safronov, Peter P.

    2018-02-01

    New Sr isotope data from well-preserved aragonite ammonoid shell material from the Mesozoic are compared with that from a living Nautilus shell. The prominent negative Sr isotope excursions known from the Middle Permian, Jurassic and Cretaceous probably have their origins in intensive plate tectonic activity, followed by enhanced hydrothermal activity at the mid-ocean ridges (mantle volcanism) which supplied low radiogenic Sr to seawater. The maximum positive (radiogenic) shift in the lower Mesozoic Sr isotope curve (Lower Triassic peak) was likely caused by a significant expansion of dry land surfaces (Dabie-Sulu Triassic orogeny) and their intensive silicate weathering in conditions of extreme warming and aridity in the very end of the Smithian, followed by warm and humid conditions in the late Spathian, which apparently resulted in a significant oceanic input of radiogenic Sr through riverine flux. The comparatively high 87Sr/86Sr ratio obtained from the living Nautilus shell is probably a function of both the Alpine orogeny, which was accompanied by significant continental weathering and input of radiogenic Sr to the oceans, and the weakening of mantle volcanism.

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

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Derry, L.A.; Keto, L.S.; Jacobsen, S.B.

    1989-09-01

    The authors report initial {sup 87}Sr/{sup 86}Sr values from an Upper Proterozoic carbonate succession from Svalbard and East Greenland. This succession, now tectonically separated into three sequences, is thick, relatively continuous, and well preserved. The relative ages of the samples from within the basin are well constrained by litho-, bio-, and chemostratigraphic techniques. The data from this study and related data from the literature are used to construct a curve of {sup 87}Sr/{sup 86}Sr for Upper Proterozoic seawater. The new data reported in this study substantially improve the isotopic record of Sr in seawater for the period between 650 andmore » 800 Ma. The data indicate that {Delta}{sup 87}Sr values of seawater were variable but low ({Delta}{sup 87}Sr {approximately}{minus}500 to {minus}250) between 900 and 650 Ma, and rose rapidly to {approximately} +30 by 600 Ma. The range of variation of {Delta}{sup 87}Sr in seawater during the Riphean-Vendian exceeds the entire range of {Delta}{sup 87}Sr in seawater during the Phanerozoic. While variation in the average isotopic composition of Sr delivered to the oceans by rivers can account for some of the observed range, changes in the ratio of submarine hydrothermal flux to river water (continental) flux are responsible for the large variation in seawater Sr isotopic composition. Changes in the continental flux of Sr to the oceans can be related to tectonic factors. Large changes in the hydrothermal flux to river water flux ratio indicated by the data could have significant consequences for the chemistry of the ocean-atmosphere system.« less

  9. 87Sr/86Sr isotopes in grapes of different cultivars: A geochemical tool for geographic traceability of agriculture products.

    PubMed

    Tescione, Ines; Marchionni, Sara; Casalini, Martina; Vignozzi, Nadia; Mattei, Massimo; Conticelli, Sandro

    2018-08-30

    87 Sr/ 86 Sr was determined on fresh red and white grapes, soils and rocks from three selected vineyards to verify the isotopic relationships between the fruit of the vine and geologic substrata of vineyards. 87 Sr/ 86 Sr were determined on sampled grapes of four different harvest years and different grape varieties, on bioavailable fraction of soils, on whole soils, and on bedrocks from the geo-pedological substratum of the vineyards. The vineyards chosen for the experimental works belong to an organic farming winery and thus cultivation procedures were strictly controlled. Grapes were sampled during the harvests of four different but consecutive years with 87 Sr/ 86 Sr that does not change reflecting the values of the soil bioavailable fraction. No variations among grapes from different vine cultivars were observed. A strict isotope relationship with soil bio-available fraction was observed. These findings demonstrate the reliability of 87 Sr/ 86 Sr, even at a very small scale, for food products geographic origin assessment. Copyright © 2018 Elsevier Ltd. All rights reserved.

  10. Application of LA-MC-ICP-MS for analysis of Sr isotope ratios in speleothems

    NASA Astrophysics Data System (ADS)

    Weber, Michael; Scholz, Denis; Wassenburg, Jasper A.; Jochum, Klaus Peter; Breitenbach, Sebastian

    2017-04-01

    Speleothems are well established climate archives. In order to reconstruct past climate variability, several geochemical proxies, such as δ13C and δ18O as well as trace elements are available. Since several factors influence each individual proxy, robust interpretation is often hampered. This calls for multi-proxy approaches involving additional isotope systems that can help to delineate the role of different sources of water within the epikarst and changes in soil composition. Sr isotope ratios (87Sr/86Sr) have been shown to provide useful information about water residence time and water mixing in the host rock. Furthermore, Sr isotopes are not fractionated during calcite precipitation, implying that the 87Sr/86Sr ratio of the speleothem provides a direct record of the drip water. While most speleothem studies applying Sr isotopes used the TIMS methodology, LA-MC-ICP-MS has been utilized for several other archives, such as otoliths and teeth. This method provides the advantage of faster data acquisition, higher spatial resolution, larger sample throughput and the absence of chemical treatment prior to analysis. Here we present the first LA-MC-ICP-MS Sr isotope data for speleothems. The analytical uncertainty of our LA-MC-ICP-MS Sr data is in a similar range as for other carbonate materials. The results of different ablation techniques (i.e. line scan and spots) are reproducible within error, implying that the application of this technique on speleothems is possible. In addition, several comparative measurements of different carbonate reference materials (i.e. MACS-3, JCt-1, JCp-1), such as tests with standard bracketing and comparison of the 87Sr/86Sr ratios with nanosecond laser ablation system and a state-of-the-art femtosecond laser ablation system, show the robustness of the method. We applied the method to samples from Morocco (Grotte de Piste) and India (Mawmluh Cave). Our results show only very small changes in the 87Sr/86Sr ratios of both speleothems

  11. Sr, Nd, and Pb Isotopic Geochemistry of Rhyolites from the Eastern Rhodopes, Bulgaria

    NASA Astrophysics Data System (ADS)

    Ivanova, R.; Kamenov, G. D.; Yanev, Y.

    2002-12-01

    Paleogene Eastern Rhodopes Volcanic Area (ERVA) is part of a more than 2000 km long magmatic belt in SE Europe extending from the Inner Dinarids (West Bosnia-Herzegovina) to Western Anatolia (European Turkey). Volcanic activity occurred during the Late Eocene-Early Oligocene and was spatially related to extensional Paleogene shallow marine basins underlain by a high-grade metamorphic basement. The volcanism is bimodal in character, with minor mafic (basalts) and major intermediate (mainly andesites) to acid (mainly rhyolites) volcanics present in similar volumes. This work focuses on Maritsa volcanic group (36-32 Ma) located in the NE part of the ERVA, S Bulgaria. The volcanic group comprises Lozen volcano composed of dacites, rhyodacites, and rhyolites, St Marina rhyolite dome, and Sheinovets rhyolite dome-cluster located within a caldera with the same name. Measured present day 87Sr/86Sr of the rhyolites range from 0.7075 to 0.7180, however on a plot 87Rb/86Sr vs 87Sr/86Sr the data form an errorchron (MSWD=21) with 30.5 +/-3.6Ma age and 87Sr/86Sr initial equal to 0.7074. Pb isotopic compositions in all of the volcanoes show similar values ranging from 18.712 to 18.768 in 206Pb/204Pb, 15.643 to 15.687 in 207Pb/204Pb, and 38.790 to 38.922 in 208Pb/204Pb. Nd isotopes show also little variations with 143Nd/144Nd ranging from 0.51242 to 0.51249. The similarity in the isotopic compositions between the volcanoes suggests common, homogeneous magmatic source. Crustal origin of the rhyolites as a result of melting of the metamorphic basement is not plausible because the rhyolites have different Sr and Nd isotopic compositions from the gneisses in the ERVA. Sr and Nd isotopic data for the rhyolites differ also from the basalts (i.e. possible mantle melts) in the Eastern Rhodopes region. Rhyolites have higher 87Sr/86Sr and lower 143Nd/144Nd ratios compared to the basalts, thus suggesting involvement of crustal component in the magma generation, most probably the metamorphic

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

    PubMed

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

    2008-01-01

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

  13. The origin of Neoproterozoic Cap Carbonates: a view from Mg and Sr Isotopes

    NASA Astrophysics Data System (ADS)

    Liu, C.; Raub, T. D.; Evans, D. A.; Wang, Z.

    2010-12-01

    Neoproterozoic cap carbonates are suggested to document Earth’s transition from a ‘snowball earth’ to an ‘extreme greenhouse’ environment. Geochemistry of these rocks is essential for its paleo-environment reconstruction, and Mg and Sr isotopes can help to understand its origin and constrain geochemical evolution of the contemporary ocean. In this study, we studied Mg and Sr isotope composition of 18 cap dolostone samples from Nuccaleena formation carbonate and one from the the mixed siliciclastic transition at its base at Elatina Creek in Adelaide Geosyncline of South Australia. We established a step-leaching procedure using ammonium acetate, various concentrations of acetic acid, and HCl on four of these cap carbonate samples to untangle the isotopic signatures of its various constituent phases. 87Sr/86Sr values of the leachates in each sample decrease continuously as leaching process proceeds and sometimes rebound as silicates are dissolved. The lowest leachate 87Sr/86Sr values, down to 0.7084, are lower than the reported dolostone(~0.7096) but still higher than those of limestones overlying the dolostone in other basins(~0.7079), indicating an input of increasing level of weathering to the ocean over the course of cap-carbonate precipitation. In contrast, δ26MgDSM3 variation with progressing leaching steps exhibits a wave pattern (variation up to 0.4~0.5‰) during the leaching processes, due to different chemical affinity of Mg in various mineral phases. More importantly, Mg isotope composition of the portion that is associated with stratigraphically low, minimum Sr isotope composition is similar to those of contemporary corals (or inorganic aragonite precipitation), but up to ca. 0.6 per mil lower than stratigraphically-higher values, suggesting a warmer weather and/or more significant silicate weathering than contemporary Earth’s climate, and a transition from physical weathering to chemical weather during deglaciation.

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

    NASA Astrophysics Data System (ADS)

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

    2014-05-01

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

  15. High-resolution dating of deep-sea clays using Sr isotopes in fossil fish teeth

    NASA Astrophysics Data System (ADS)

    Ingram, B. Lynn

    1995-09-01

    Strontium isotopic compostitions of ichthyoliths (microscopic fish remains) in deep-sea clays recovered from the North Pacific Ocean (ODP holes 885A, 886B, and 886C) are used to provide stratigraphic age control within these otherwise undatable sediments. Age control within the deep-sea clays is crucial for determining changes in sedimentation rates, and for calculating fluxes of chemical and mineral components to the sediments. The Sr isotopic ages are in excellent agreement with independent age datums from above (diatom ooze), below (basalt basement) and within (Cretaceous-Tertiary boundary) the clay deposit. The 87Sr/ 86Sr ratios of fish teeth from the top of the pelagic clay unit (0.708989), indicate an Late Miocene age (5.8 Ma), as do radiolarian and diatom biostratigraphic ages in the overlying diatom ooze. The 87Sr/ 86Sr ratio (0.707887) is consistent with a Cretaceous-Tertiary boundary age, as identified by anomalously high iridium, shocked quartz, and sperules in Hole 886C. The 87Sr/ 86Sr ratios of pretreated fish teeth from the base of the clay unit are similar to Late Cretaceous seawater (0.707779-0.707519), consistent with radiometric ages from the underlying basalt of 81 Ma. Calculation of sedimentation rates based on Sr isotopic ages from Hole 886C indicate an average sedimentation rate of 17.7 m/Myr in Unit II (diatom ooze), 0.55 m/Myr in Unit IIIa (pelagic clay), and 0.68 m/Myr in Unit IIIb (distal hydrothermal precipitates). The Sr isotopic ages indicate a period of greatly reduced sedimentation (or possible hiatus) between about 35 and 65 Ma (Eocene-Paleocene), with a linear sedimentation rate of only 0.04 m/Myr The calculated sedimentation rates are generally inversely proportional to cobalt accumulation rates and ichthyolith abundances. However, discrepancies between Sr isotope ages and cobalt accumulation ages of 10-15 Myr are evident, particularly in the middle of the clay unit IIIa (Oligocene-Paleocene).

  16. Migration and rearing histories of chinook salmon (Oncorhynchus tshawytscha) determined by ion microprobe Sr isotope and Sr/Ca transects of otoliths

    USGS Publications Warehouse

    Bacon, C.R.; Weber, P.K.; Larsen, K.A.; Reisenbichler, R.; Fitzpatrick, J.A.; Wooden, J.L.

    2004-01-01

    Strontium isotope and Sr/Ca ratios measured in situ by ion microprobe along radial transects of otoliths of juvenile chinook salmon (Oncorhynchus tshawytscha) vary between watersheds with contrasting geology. Otoliths from ocean-type chinook from Skagit River estuary, Washington, had prehatch regions with 87Sr/86Sr ratios of ???0.709, suggesting a maternally inherited marine signature, extensive fresh water growth zones with 87Sr/86Sr ratios similar to those of the Skagit River at ???0.705, and marine-like 87Sr/86Sr ratios near their edges. Otoliths from stream-type chinook from central Idaho had prehatch 87Sr/86Sr ratios ???0.711, indicating that a maternal marine Sr isotopic signature is not preserved after the ???1000- to 1400-km migration from the Pacific Ocean. 87Sr/86Sr ratios in the outer portions of otoliths from these Idaho juveniles were similar to those of their respective streams (???0.708-0.722). For Skagit juveniles, fresh water growth was marked by small decreases in otolith Sr/Ca, with increases in Sr/Ca corresponding to increases in 87Sr/86Sr with migration into salt water. Otoliths of Idaho fish had Sr/Ca radial variation patterns that record seasonal fluctuation in ambient water Sr/Ca ratios. The ion microprobe's ability to measure both 87Sr/86Sr and Sr/Ca ratios of otoliths at high spatial resolution in situ provides a new tool for studies of fish rearing and migration. ?? 2004 NRC Canada.

  17. Sr Isotopes at the Onset of the Ice Ages at the Northern Apennines

    NASA Astrophysics Data System (ADS)

    Fuchs, Rita; Lazar, Boaz; Angiolini, Lucia; Crippa, Gaia; Stein, Mordechai

    2017-04-01

    Sr isotopes can be used to constrain the marine Sr budget. The temporal variations in the 87Sr/86Sr ratios (radiogenic Sr) have been reconstructed over the past few decades based on marine macro and micro fossils data (e.g. brachiopods and foraminifera). It is used to constrain the sources and amounts of strontium that dictate the temporal variations in oceanic Sr throughout the Phanerozoic. On the other hand, the study of processes controlling the composition stable Sr isotopes (δ88/86Sr) is very new and only limited research was conducted on this topic during the past few years. Up to date, no δ88/86Sr data are available for considerable parts of Earth's history and the contribution of the potential Sr sources to the oceans is poorly constrained. Here, we set to examine the behavior of radiogenic and stable Sr isotopes in the marine environment of the northern Apennines (Italy) during the time interval of the late Pliocene to early-Middle Pleistocene - upon the onset of ice ages in the northern latitudes. We collected fossil mollusks from outcrops of the Arda and Stirone Rivers that are rich in bivalves, brachiopods, foraminifera (that were used for establishing the chronostratigraphy of the sections) and other genera. Ecological and sedimentological analysis of the section suggest a normal marine environment of depth range of several tens of meters that existed on the southern flanks of the large Po embayment. In order to evaluate the potential of the fossil assemblages in the Arda and Stirone sections to serve as reliable recorders of the marine δ88/86Sr of seawater during the desired period, we examined mineralogical and chemical properties of the fossils (e.g. distribution of trace elements like Sr and Mg in the skeletons, microstructures like secondary fillings of punctate shells in brachiopod) and measured the 87Sr/86Sr ratios. Among the species analyzed, Aequipecten opercularis (bivalve) and Glycymeris inflata (bivalve) have aragonite skeletons that

  18. Effect of Wood Aging on Wine Mineral Composition and 87Sr/86Sr Isotopic Ratio.

    PubMed

    Kaya, Ayse D; Bruno de Sousa, Raúl; Curvelo-Garcia, António S; Ricardo-da-Silva, Jorge M; Catarino, Sofia

    2017-06-14

    The evolution of mineral composition and wine strontium isotopic ratio 87 Sr/ 86 Sr (Sr IR) during wood aging were investigated. A red wine was aged in stainless steel tanks with French oak staves (Quercus sessiliflora Salisb.), with three industrial scale replicates. Sampling was carried out after 30, 60, and 90 days of aging, and the wines were evaluated in terms of general analysis, phenolic composition, total polysaccharides, multielement composition, and Sr IR. Li, Be, Mg, Al, Sc, Ti, V, Mn, Co, Ni, Cu, Zn, Ga, Ge, As, Rb, Sr, Y, Zr, Mo, Sb, Cs, Ba, Pr, Nd, Sm, Eu, Dy, Ho, Er, Yb, Lu, Tl, and Pb elements and 87 Sr/ 86 Sr were determined by quadrupole inductively coupled plasma mass spectrometry (Q-ICP-MS) and Na, K, Ca, and Fe by flame atomic absorption spectrometry (FAAS). Two-way ANOVA was applied to assess wood aging and time effect on Sr IR and mineral composition. Wood aging resulted in significantly higher concentrations of Mg, V, Co, Ni, and Sr. At the end of the aging period, wine exhibited statistically identical Sr IR compared to control. Study suggests that wood aging does not affect 87 Sr/ 86 Sr, not precluding the use of this parameter for wine traceability purposes.

  19. Sr Isotopes and Migration of Prairie Mammoths (Mammuthus columbi) from Laguna de las Cruces, San Luis Potosi, Mexico

    NASA Astrophysics Data System (ADS)

    Solis-Pichardo, G.; Perez-Crespo, V.; Schaaf, P. E.; Arroyo-Cabrales, J.

    2011-12-01

    Asserting mobility of ancient humans is a major issue for anthropologists. For more than 25 years, Sr isotopes have been used as a resourceful tracer tool in this context. A comparison of the 87Sr/86Sr ratios found in tooth enamel and in bone is performed to determine if the human skeletal remains belonged to a local or a migrant. Sr in bone approximately reflects the isotopic composition of the geological region where the person lived before death; whereas the Sr isotopic system in tooth enamel is thought to remain as a closed system and thus conserves the isotope ratio acquired during childhood. Sr isotope ratios are obtained through the geologic substrate and its overlying soil, from where an individual got hold of food and water; these ratios are in turn incorporated into the dentition and skeleton during tissue formation. In previous studies from Teotihuacan, Mexico we have shown that a three-step leaching procedure on tooth enamel samples is important to assure that only the biogenic Sr isotope contribution is analyzed. The same Sr isotopic tools can function concerning ancient animal migration patterns. To determine or to discard the mobility of prairie mammoths (Mammuthus columbi) found at Laguna de las Cruces, San Luis Potosi, México the leaching procedure was applied on six molar samples from several fossil remains. The initial hypothesis was to use 87Sr/86Sr values to verify if the mammoth population was a mixture of individuals from various herds and further by comparing their Sr isotopic composition with that of plants and soils, to confirm their geographic origin. The dissimilar Sr results point to two distinct mammoth groups. The mammoth population from Laguna de Cruces was then not a family unit because it was composed by individuals originated from different localities. Only one individual was identified as local. Others could have walked as much as 100 km to find food and water sources.

  20. Determination of 90Sr / 238U ratio by double isotope dilution inductively coupled plasma mass spectrometer with multiple collection in spent nuclear fuel samples with in situ 90Sr / 90Zr separation in a collision-reaction cell

    NASA Astrophysics Data System (ADS)

    Isnard, H.; Aubert, M.; Blanchet, P.; Brennetot, R.; Chartier, F.; Geertsen, V.; Manuguerra, F.

    2006-02-01

    Strontium-90 is one of the most important fission products generated in nuclear industry. In the research field concerning nuclear waste disposal in deep geological environment, it is necessary to quantify accurately and precisely its concentration (or the 90Sr / 238U atomic ratio) in irradiated fuels. To obtain accurate analysis of radioactive 90Sr, mass spectrometry associated with isotope dilution is the most appropriated method. But, in nuclear fuel samples the interference with 90Zr must be previously eliminated. An inductively coupled plasma mass spectrometer with multiple collection, equipped with an hexapole collision cell, has been used to eliminate the 90Sr / 90Zr interference by addition of oxygen in the collision cell as a reactant gas. Zr + ions are converted into ZrO +, whereas Sr + ions are not reactive. A mixed solution, prepared from a solution of enriched 84Sr and a solution of enriched 235U was then used to quantify the 90Sr / 238U ratio in spent fuel sample solutions using the double isotope dilution method. This paper shows the results, the reproducibility and the uncertainties that can be obtained with this method to quantify the 90Sr / 238U atomic ratio in an UOX (uranium oxide) and a MOX (mixed oxide) spent fuel samples using the collision cell of an inductively coupled plasma mass spectrometer with multiple collection to perform the 90Sr / 90Zr separation. A comparison with the results obtained by inductively coupled plasma mass spectrometer with multiple collection after a chemical separation of strontium from zirconium using a Sr spec resin (Eichrom) has been performed. Finally, to validate the analytical procedure developed, measurements of the same samples have been performed by thermal ionization mass spectrometry, used as an independent technique, after chemical separation of Sr.

  1. Geochemical and Sr isotopic variations in groundwaters of the Edwards aquifer, central Texas

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Oetting, G.C.; Banner, J.L.; Sharp, J.M. Jr.

    1992-01-01

    The regionally-extensive Edwards aquifer of central Texas lies on the northwestern edge of the Gulf of Mexico Basin. The aquifer system is composed primarily of lower Cretaceous marine limestones and dolostones with minor evaporitic and siliciclastic confining units of the Edwards Group and associated formations. The eastern and southern boundaries of the freshwater aquifer are defined by an abrupt change in groundwater salinity that is known as the badwater line. Variation in the isotopic composition and concentration of Sr in the mineral phases and waters in this aquifer system provide means to examine groundwater evolution processes. Models of simultaneous variationsmore » in Sr isotopes and major and trace ions are used to constrain processes of groundwater-rock interaction and groundwater mixing. Geochemical variations were examined in Edwards carbonate host rocks and groundwaters in Williamson and Bell Counties. Groundwaters were sampled along and across the badwater line, and range in salinity from 320--2,630 mg/l total dissolved solids. Major ion distributions in the water samples demonstrate a hydrochemical facies transition from Ca-HCO[sub 3] freshwaters to Na-Cl-SO[sub 4]-HCO[sub 3] badwaters. Both water types show a wide range of [sup 87]Sr/[sup 86]Sr values: Ca-HCO[sub 3] waters range from values of 0.7078--0.7093, and Na-Cl-SO[sub 4]-HCO[sub 3] waters range from values of 0.7087--0.7097. The Sr isotope compositions for both water groups are significantly greater than their host marine carbonates ([approximately]0.7075). The high Sr isotopic compositions indicate an extraformational source of Sr in both hydrochemical facies. Fluid mixing processes involving a freshwater and at least two badwater endmembers are required to account for variations in elemental and isotopic compositions in the groundwaters. Mineral-solution reactions may operate during and/or subsequent to mixing to produce the compositional variability observed in some intermediate

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

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Wall, Andy; Jain, Jinesh; Stewart, Brian

    2012-01-01

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

  3. Heterogeneity of the Caribbean plateau mantle source: Sr, O and He isotopic compositions of olivine and clinopyroxene from Gorgona Island

    NASA Astrophysics Data System (ADS)

    Révillon, S.; Chauvel, C.; Arndt, N. T.; Pik, R.; Martineau, F.; Fourcade, S.; Marty, B.

    2002-12-01

    The composition of the mantle plumes that created large oceanic plateaus such as Ontong Java or the Caribbean is still poorly known. Geochemical and isotopic studies on accreted portions of the Caribbean plateau have shown that the plume source was heterogeneous and contained isotopically depleted and relatively enriched portions. A distinctive feature of samples from the Caribbean plateau is their unusual Sr isotopic compositions, which, at a given Nd isotopic ratio, are far higher than in samples from other oceanic plateaus. Sr, O and He isotopic compositions of whole rocks and magmatic minerals (clinopyroxene or olivine) separated from komatiites, gabbros and peridotites from Gorgona Island in Colombia were determined to investigate the origin of these anomalously radiogenic compositions. Sequentially leached clinopyroxenes have Sr isotopic compositions in the range 87Sr/ 86Sr=0.70271-0.70352, systematically lower than those of leached and unleached whole rocks. Oxygen isotopic ratios of clinopyroxene vary within the range δ 18O=5.18-5.35‰, similar to that recorded in oceanic island basalts. He isotopic ratios are high ( R/ Ra=8-19). The lower 87Sr/ 86Sr ratios of most of the clinopyroxenes shift the field of the Caribbean plateau in Nd-Sr isotope diagrams toward more 'normal' values, i.e. a position closer to the field defined by mid-ocean ridge basalts and oceanic-island basalts. Three clinopyroxenes have slightly higher 87Sr/ 86Sr ratios that cannot be explained by an assimilation model. The high 87Sr/ 86Sr and variations of 143Nd/ 144Nd are interpreted as a source characteristic. Trace-element ratios, however, are controlled mainly by fractionation during partial melting. We combine these isotopic data in a heterogeneous plume source model that accounts for the diversity of isotopic signatures recorded on Gorgona Island and throughout the Caribbean plateau. The heterogeneities are related to old recycled oceanic lithosphere in the plume source; the high 3

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

    USGS Publications Warehouse

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

    1986-01-01

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

  5. Isotopic reconstruction of ancient human migrations: A comprehensive Sr isotope reference database for France and the first case study at Tumulus de Sables, south-western France

    NASA Astrophysics Data System (ADS)

    Willmes, M.; Boel, C.; Grün, R.; Armstrong, R.; Chancerel, A.; Maureille, B.; Courtaud, P.

    2012-04-01

    Strontium isotope ratios (87Sr/86Sr) can be used for the reconstruction of human and animal migrations across geologically different terrains. Sr isotope ratios in rocks are a product of age and composition and thus vary between geologic units. From the eroding environment Sr is transported into the soils, plants and rivers of a region. Humans and animals incorporate Sr from their diet into their bones and teeth, where it substitutes for calcium. Tooth enamel contains Sr isotope signatures acquired during childhood and is most resistant to weathering and overprinting, while the dentine is often diagenetically altered towards the local Sr signature. For the reconstruction of human and animal migrations the tooth enamel 87Sr/86Sr ratio is compared to the Sr isotope signature in the vicinity of the burial site and the surrounding area. This study focuses on the establishment of a comprehensive reference map of bioavailable 87Sr/86Sr ratios for France. In a next step we will compare human and animal teeth from key archaeological sites to this reference map to investigate mobility. So far, we have analysed plant and soil samples from ~200 locations across France including the Aquitaine basin, the western and northern parts of the Paris basin, as well as three transects through the Pyrenees Mountains. The isotope data, geologic background information (BRGM 1:1M), field images, and detailed method descriptions are available through our online database iRhum (http://rses.anu.edu.au/research/ee). This database can also be used in forensic studies and food sciences. As an archaeological case study teeth from 16 adult and 8 juvenile individuals were investigated from an early Bell Beaker (2500-2000 BC) site at Le Tumulus des Sables, south-west France (Gironde). The teeth were analysed for Sr isotope ratios using laser ablation ICP-MS. Four teeth were also analysed using solution ICP-MS, which showed a significant offset to the laser ablation results. This requires further

  6. A Sr and Mg isotopic study of soil and stream waters along an erosional gradient, Sierra Nevada, California

    NASA Astrophysics Data System (ADS)

    Rosen, V. B.; Maher, K.; Kouba, C. M.; Weinman, B. A.; Yoo, K.; Mudd, S. M.

    2012-12-01

    Since chemical weathering rates are proposed to regulate atmospheric CO2 concentrations and by extension global temperature over geologic timescales, understanding the relationship between chemical weathering rates and physical erosion is crucial to accurately interpreting Earth's climate history. The rate of supply of fresh minerals to the weathering zone is known to be an important control on chemical weathering rates. However, the consequences of physical erosion on the isotopic composition of weathering-derived solutes are more difficult to assess. This study capitalizes on a series of granitic hillslope transects with different erosion rates but similar climate, vegetation, and bedrock, in order to assess the consequences of erosion on the Sr and Mg isotopic composition of solutes. Reactive transport model simulations of varying complexity have been used to complement the field measurements and to analyze the sensitivity of fluid isotopic compositions to changes in key parameters such as erosion rate, flow rate, and biological cycling. The three hillslopes in the Feather River Basin, California reflect different degrees of channel erosion at their bases—BRC is a hillslope with active channel incision (60% average slope, below the knickpoint), FTA is a hillslope reflecting the transition between the relict and modern-day incising areas (50% average slope, at the knickpoint), and POMD is a 30% average hillslope in the relict landscape above the knickpoint. We measured the major element compositions, as well as the Sr and Mg isotopic compositions of soil water leaches (deionized water leaches), lysimeters, stream waters, and groundwaters by multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS). The 87Sr/86Sr values of soil and stream waters show minimal variation (0.7042 to 0.7046) as a function of soil depth, erosion rate, or sampling season despite abundant radiogenic biotite in the profiles. These results agree with the reactive transport

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

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

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

    NASA Technical Reports Server (NTRS)

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

    2012-01-01

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

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

    USGS Publications Warehouse

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

    2012-01-01

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

  10. 87Sr/ 86Sr Concentrations in the Appalachian Basin: A Review

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Mordensky, Stanley P.; Lieuallen, A. Erin; Verba, Circe

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

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

    NASA Astrophysics Data System (ADS)

    Wiegand, B. A.; Schwendenmann, L.

    2013-04-01

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

  12. A Sr-isotopic comparison between thermal waters, rocks, and hydrothermal calcites, Long Valley caldera, California

    USGS Publications Warehouse

    Goff, F.; Wollenberg, H.A.; Brookins, D.C.; Kistler, R.W.

    1991-01-01

    The 87Sr/86Sr values of thermal waters and hydrothermal calcites of the Long Valley caldera geothermal system are more radiogenic than those of young intracaldera volcanic rocks. Five thermal waters display 87Sr/86Sr of 0.7081-0.7078 but show systematically lighter values from west to east in the direction of lateral flow. We believe the decrease in ratio from west to east signifies increased interaction of deeply circulating thermal water with relatively fresh volcanic rocks filling the caldera depression. All types of pre-, syn-, and post-caldera volcanic rocks in the west and central caldera have (87Sr/86Sr)m between about 0.7060 and 0.7072 and values for Sierra Nevada granodiorites adjacent to the caldera are similar. Sierran pre-intrusive metavolcanic and metasedimentary rocks can have considerably higher Sr-isotope ratios (0.7061-0.7246 and 0.7090-0.7250, respectively). Hydrothermally altered volcanic rocks inside the caldera have (87Sr/86Sr)m slightly heavier than their fresh volcanic equivalents and hydrothermal calcites (0.7068-0.7105) occupy a midrange of values between the volcanic/plutonic rocks and the Sierran metamorphic rocks. These data indicate that the Long Valley geothermal reservoir is first equilibrated in a basement complex that contains at least some metasedimentary rocks. Reequilibration of Sr-isotope ratios to lower values occurs in thermal waters as convecting geothermal fluids flow through the isotopically lighter volcanic rocks of the caldera fill. ?? 1991.

  13. Stable and Radiogenic Sr Isotopes in Barite - Clues on the Links Between Weathering, Climate and the C Cycle

    NASA Astrophysics Data System (ADS)

    Paytan, A.; Eisenhauer, A.; Wallmann, K. J. G.; Griffith, E. M.; Ridgwell, A.

    2017-12-01

    The radiogenic Sr-isotopic signature (87Sr/86Sr) of seawater fluctuates primarily in response to changes in the inputs of Sr from weathering and hydrothermal activity, which have distinct 87Sr/86Sr values. Changes in the isotopic ratio of the weathered terrain also contribute to observed changes in 87Sr/86Sr. The stable Sr-isotope ratios in seawater (mass dependent isotopic fractionation; δ88/86Sr) fluctuate primarily in response to the rate of calcium carbonate (CaCO3) accumulation at the seafloor. Together the radiogenic and stable Sr can constrain the coupling between weathering and sedimentation and shed light on the relation between weathering, CaCO3 deposition, the global carbon (C) cycle and climate. Reconstruction of the coupled stable and radiogenic Sr seawater curves over the past 35 Ma of Earth history indicates that the location and rate of CaCO3 burial in the ocean fluctuated considerably over the past 35 Ma. Between 35 to 18 Ma a reduction in neritic CaCO3 burial and increased burial in pelagic settings is observed. The trend was reversed between 20 and 3 Ma and finally over the last 3 million years a rapid change from neritic to pelagic burial is seen. The lack of continues increase of pelagic CaCO3 burial rates suggests that silicate weathering rates have not increased monotonically over the past 35 Ma implying strong feedbacks operating in the climate system - lower atmospheric pCO2 and cooling trends (which control chemical weathering as seen from carbonate deposition in the ocean) countered the effects of uplift (which controls physical weathering) - modulating weathering rates and preventing a runaway ice-house. In addition the data suggests considerable fluctuations in seawater Sr concentrations over time. These data demonstrate how using multiple isotope proxies can help constrain interpretations of the geological record.

  14. Multiple enrichment of the Carpathian-Pannonian mantle: Pb-Sr-Nd isotope and trace element constraints

    NASA Astrophysics Data System (ADS)

    Rosenbaum, Jeffrey M.; Wilson, Marjorie; Downes, Hilary

    1997-07-01

    Pb isotope compositions of acid-leached clinopyroxene and amphibole mineral separates from spinel peridotite mantle xenoliths entrained in Tertiary-Quaternary alkali basalts from the Carpathian-Pannonian Region of eastern Europe provide important constraints on the processes of metasomatic enrichment of the mantle lithosphere in an extensional tectonic setting associated with recent subduction. Principal component analysis of Pb-Sr-Nd isotope and rare earth element compositions of the pyroxenes is used to identify the geochemical characteristics of the original lithospheric mantle protolith and a spectrum of infiltrating metasomatic agents including subduction-related aqueous fluids and silicate melts derived from a subduction-modified mantle wedge which contains a St. Helena-type (HIMU) plume component. The mantle protolith is highly depleted relative to mid-ocean ridge basalt-source mantle with Pb-Nd-Sr isotope compositions consistent with an ancient depletion event. Silicate melt infiltration into the protolith accounts for the primary variance in the Pb-Sr-Nd isotope compositions of the xenoliths and has locally generated metasomatic amphibole. Infiltration of aqueous fluids has introduced radiogenic Pb and Sr without significantly perturbing the rare earth element signature of the protolith. The Pb isotope compositions of the fluid-modified xenoliths suggest that they reacted with aqueous fluids released from a subduction zone which had equilibrated with sediment derived from an ancient basement terrain. We propose a model for mantle lithosphere evolution consistent with available textural and geochemical data for the xenolith population. The Pb-Sr-Nd isotope compositions of both alkaline mafic magmas and rare, subduction-related, calc-alkaline basaltic andesites from the region provide important constraints for the nature of the asthenospheric mantle wedge and confirm the presence of a HIMU plume component. These silicate melts contribute to the metasomatism

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  16. Ca and Sr isotope records support ocean acidification during end-Permian mass extinction

    NASA Astrophysics Data System (ADS)

    Wang, J.; Jacobson, A. D.; Zhang, H.; Ramezani, J.; Sageman, B. B.; Hurtgen, M.; Bowring, S. A.; Shen, S.

    2017-12-01

    The end-Permian mass extinction represents the most devastating loss of biodiversity during the Phanerozoic. A negative carbon isotope (δ13C) excursion that accompanies the event suggests a significant perturbation to the global carbon cycle, likely induced by CO2 emissions during eruption of the Siberian Traps large igneous province. The carbon cycle is linked with the Ca and Sr cycles through chemical weathering and carbonate precipitation. Therefore, analyses of Ca (δ44/40Ca), radiogenic Sr (87Sr/86Sr), and stable Sr (δ88/86Sr) isotope abundance variations in marine carbonate rocks spanning the Permian-Triassic Boundary (PTB) can reveal key information about biogeochemical changes that occurred during this time. We report δ44/40Ca, 87Sr/86Sr, and δ88/86Sr records analyzed by TIMS for the Meishan and Dajiang sections in China. δ44/40Ca values exhibit similar patterns in both sections. The values remain unchanged across the extinction event layer (EXT) and then decrease by 0.20‰ before increasing by 0.20‰ to 0.40‰ around the PTB. In the Meishan section, 87Sr/86Sr ratios increase after the EXT and return to pre-excursion levels by the PTB. Simultaneously, δ88/86Sr values decrease by 0.12‰ across the EXT and increase by 0.08‰ by the PTB. The patterns of our data support the hypothesis that elevated atmospheric CO2 levels enhanced chemical weathering inputs and might have caused transient ocean acidification, with an "alkalinity overshoot" and increased carbonate deposition occurring after the extinction. Additional measurements and model calculations are underway to help refine and improve these preliminary interpretations.

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

    NASA Technical Reports Server (NTRS)

    Hui. Hejiu; Neal, Clive, R.; Shih, Chi-Yu; Nyquist, Laurence E.

    2012-01-01

    Pristine Apollo 14 (A-14) high-Al basalts represent the oldest volcanic deposits returned from the Moon [1,2] and are relatively enriched in Al2O3 (>11 wt%) compared to other mare basalts (7-11 wt%). Literature Rb-Sr isotopic data suggest there are at least three different eruption episodes for the A-14 high-Al basalts spanning the age range approx.4.3 Ga to approx.3.95 Ga [1,3]. Therefore, the high-Al basalts may record lunar mantle evolution between the formation of lunar crust (approx.4.4 Ga) and the main basin-filling mare volcanism (<3.85 Ga) [4]. The high-Al basalts were originally classified into five compositional groups [5,6], and then regrouped into three with a possible fourth comprising 14072 based on the whole-rock incompatible trace element (ITE) ratios and Rb-Sr radiometric ages [7]. However, Rb-Sr ages of these basalts from different laboratories may not be consistent with each other because of the use of different 87Rb decay constants [8] and different isochron derivation methods over the last four decades. This study involved a literature search for Rb-Sr isotopic data previously reported for the high-Al basalts. With the re-calculated Rb-Sr radiometric ages, eruption episodes of A-14 high-Al basalts were determined, and their petrogenesis was investigated in light of the "new" Rb-Sr isotopic data and published trace element abundances of these basalts.

  18. Petrogenesis of ultramafic xenoliths from Hawaii inferred from Sr, Nd, and Pb isotopes

    NASA Astrophysics Data System (ADS)

    Okano, Osamu; Tatsumoto, Mitsunobu

    Isotopic compositions of Nd, Sr, and Pb in xenoliths in the Honolulu volcanic series from the Salt Lake Crater (H-type) are similar to those of the host post-erosional basalts, but are distinct from the magma sources of Koolau shield tholeiites and MORB. In contrast, one spinel Iherzolite (K-type) has isotopic compositions of Nd and Sr that are close to those of Koolau tholeiite rather than to the other Hawaiian basalts. Previous studies have shown that Sr isotopic composition of the xenoliths and the host basalt and that trace element concentrations in minerals of garnet Iherzolites from Honolulu basalt were nearly in equilibrium with the host magma, indicating that Honolulu volcanics were derived from garnet Iherzolite or similar material. However, differences exist among the isotopic compositions (especially Nd) of the xenoliths indicating that they are accidental inclusions from upper layers. The similarity in isotopic compositions between xenoliths and Honolulu basalt suggests that the source areas in the mantle are chemically similar. Correlation of 238U/204Pb vs. 206Pb/204Pb of chrome diopside separated from the H-type spinel Iherzolites indicates that the xenoliths are 80±36 Ma, which corresponds to the lithosphere age of the Hawaiian site. This age is consistent with petrological studies [e.g., Sen and Leeman, 1991] which have found that the spinel Iherzolite inclusions are derived from the lithosphere wall rocks. The ɛNd = ˜+8 of the H-xenoliths is slightly lower than that for the East Pacific Rise MORB indicating that the xenoliths are derived from a trace element depleted source similar to the MORB residue. If the garnet Iherzolite xenoliths are derived from mixture of spinel Iherzolite with intrusive pyroxenite, then the source of the pyroxenite contained little plume component. The one exceptional spinel Iherzolite xenolith may be a residue of Koolau-like tholeiitic magma or may have been metasomatized by Koolau volcanism in the deep lithosphere

  19. The Origin and Evolution of Nucleosynthetic Sr Isotope Variability in Calcium and Aluminum-rich Refractory Inclusions

    NASA Astrophysics Data System (ADS)

    Myojo, Kunihiro; Yokoyama, Tetsuya; Okabayashi, Satoki; Wakaki, Shigeyuki; Sugiura, Naoji; Iwamori, Hikaru

    2018-01-01

    Nucleosynthetic isotope anomalies in meteorites are useful for investigating the origin of materials in the protoplanetary disk and dynamical processes of planetary formation. In particular, calcium and aluminum-rich inclusions (CAIs) found in chondrites are key minerals for decoding the initial conditions of the solar system before the accretion of small planetary bodies. In this study, we report isotopic analyses for three Allende CAIs, fluffy type A (FTA), type B, and fine-grained spinel rich (FS) inclusions, with a specific emphasis on the measurements of 84Sr/86Sr ratios. It was found that the average μ 84Sr values (106 relative deviations from a standard material) were 175, 129, and 56 ppm for the samples of FTA, type B, and FS inclusions, respectively. Additionally, the FTA samples exhibited heterogeneous μ 84Sr values, while those for the type B and FS inclusions were homogeneous within individual inclusions. The elevated μ 84Sr values were most likely explained by the relative enrichment of r-process nuclides in the CAI formation region. The variation of μ 84Sr values between the FTA and type B inclusions, as well as within the FTA inclusion, suggests the presence of multiple CAI source reservoirs with distinct isotopic compositions, which is either inherited from isotopic heterogeneity in the molecular cloud or caused by the selective destruction of r-process-enriched supernova grains via nebular thermal processing. On the other hand, the reaction between a refractory precursor of the FS inclusion and a gaseous reservoir enriched in Mg, Si, and 16O resulted in the lowest μ 84Sr values for the FS inclusion.

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

    NASA Astrophysics Data System (ADS)

    Jørgensen, Niels; Banoeng-Yakubo, Bruce

    2001-03-01

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

  1. Sr and Nd isotopic and trace element compositions of Quaternary volcanic centers of the Southern Andes

    USGS Publications Warehouse

    Futa, K.; Stern, C.R.

    1988-01-01

    Isotopic compositions of samples from six Quaternary volcanoes located in the northern and southern extremities of the Southern Volcanic Zone (SVZ, 33-46??S) of the Andes and from four centers in the Austral Volcanic Zone (AVZ, 49-54??S) range for 87Sr 86Sr from 0.70280 to 0.70591 and for 143Nd 144Nd from 0.51314 to 0.51255. The ranges are significantly greater than previously reported from the southern Andes but are different from the isotopic compositions of volcanoes in the central and northern Andes. Basalts and basaltic andesites from three centers just north of the Chile Rise-Trench triple junction have 87Sr 86Sr, 143Nd 144Nd, La Yb, Ba La, and Hf Lu that lie within the relatively restricted ranges of the basic magmas erupted from the volcanic centers as far north as 35??S in the SVZ of the Andes. The trace element and Sr and Nd isotopic characteristics of these magmas may be explained by source region contamination of subarc asthenosphere, with contaminants derived from subducted pelagic sediments and seawater-altered basalts by dehydration of subducted oceanic lithosphere. In the northern extremity of the SVZ between 33?? and 34??S, basaltic andesites and andesites have higher 87Sr 86Sr, Rb Cs, and Hf Lu, and lower 143Nd 144Nd than basalts and basaltic andesites erupted farther south in the SVZ, which suggests involvement of components derived from the continental crust. In the AVZ, the most primitive sample, high-Mg andesite from the southernmost volcanic center in the Andes (54??S) has Sr and Nd isotopic compositions and K Rb and Ba La similar to MORB. The high La Yb of this sample suggests formation by small degrees of partial melting of subducted MORB with garnet as a residue. Samples from centers farther north in the AVZ show a regionally regular northward increase in SiO2, K2O, Rb, Ba, Ba La, and 87Sr 86Sr and decrease in MgO, Sr, K Rb, Rb Cs, and 143Nd 144Nd, suggesting increasingly greater degrees of fractional crystallization and associated intra

  2. Equilibrium-disequilibrium relations in the Monte Rosa Granite, Western Alps: Petrological, Rb-Sr and stable isotope data

    USGS Publications Warehouse

    Frey, M.; Hunziker, J.C.; O'Neil, J.R.; Schwander, H.W.

    1976-01-01

    Nine samples from the Monte Rosa Granite have been investigated by microscopic, X-ray, wet chemical, electron microprobe, stable isotope and Rb-Sr and K-Ar methods. Two mineral assemblages have been distinguished by optical methods and dated as Permian and mid-Tertiary by means of Rb-Sr age determinations. The Permian assemblage comprises quartz, orthoclase, oligoclase, biotite, and muscovite whereas the Alpine assemblage comprises quartz, microcline, albite+epidote or oligoclase, biotite, and phengite. Disequilibrium between the Permian and Alpine mineral assemblages is documented by the following facts: (i) Two texturally distinguishable generations of white K-mica are 2 M muscovite (Si=3.1-3.2) and 2 M or 3 T phengite (Si=3.3-3.4). Five muscovites show Permian Rb-Sr ages and oxygen isotope fractionations indicating temperatures between 520 and 560 ?? C; however, K-Ar ages are mixed or rejuvenated. Phengite always shows mid-Tertiary Rb-Sr ages, (ii) Two biotite generations can be recognized, although textural evidence is often ambiguous. Three out of four texturally old biotites show mid-Tertiary Rb-Sr cooling ages while the oxygen isotopic fractionations point to Permian, mixed or Alpine temperatures, (iii) Comparison of radiogenic and stable isotope relations indicates that the radiogenic isotopes in the interlayer positions of the micas were mobilized during Alpine time without recrystallization, that is, without breaking Al-O or Si-O bonds. High Ti contents in young muscovites and biotites also indicate that the octahedral (and tetrahedral) sites remained undisturbed during rejuvenation. (iv) 'Isotopic reversals' in the order of O18 enrichment between K-feldspar and albite exist. Arguments for equilibrium during Permian time are meagre because of Alpine overprinting effects. Texturally old muscovites show high temperatures and Permian Rb-Sr ages in concordancy with Rb-Sr whole rock ages. For the tectonically least affected samples, excellent concordance

  3. Source Signature of Sr Isotopes in Fluids Emitting From Mud volcanoes in Taiwan

    NASA Astrophysics Data System (ADS)

    Chung, C.; You, C.; Chao, H.

    2003-12-01

    Located at the boundary between the Philippine Sea Plate and the Asia Continental Plate, abundance of mud volcanoes were erupted on land in Taiwan. According to their occurrences and associated tectonic settings, these mud volcanoes were classified into four groupies. The group (I) mud volcanoes are located in the western coastal plane, whereas group (II) and (III) are situated near the Kutinkung anticline axis and the Chishan fault respectively. The group (IV) mud volcanoes are discovered at the Coastal Range. Although there are numerous studies focused on morphology, possible fluid migration paths and sources are poorly understood. We have collected and analyzed major ions and Sr isotopic ratios in fluids separated from various mud volcanoes in Taiwan. Chemical contents of these fluids were measured by IC and the emitted gasses were analyzed by GC. The Sr concentrations in these fluids were determined using AA and the isotopic compositions were analyzed by TIMS. The dominated ions in fluids are Na and Cl which account for 98% of dissolved materials. All fluids show similar Na/Cl ratios(0.7-0.8), slightly higher than seawater but each group has unique Sr isotopic signature. Waters expelled from group I mud volcanoes featured with low salinity and high Sr isotopic ratios ranged from 0.71150 to 0.71175. Groups II and III were outcroped in the Kutinkung formation but show distinctive chemical compositions. Group II fluids have four times Cl concentrations(358-522mM) compared with those of group III(85-162mM). The latter fluids appear to be more radiogenic(0.71012- 0.71075) indicating possible influence due to water-rock interactions. Low 87Sr/86Sr(0.70692-0.70939) is typical characteristic of mud volcano fluids in group IV where large Mg and K depletion were discovered, suggesting effects due to sediment diagenetic processes. The chemical compositions of mud volcano associated gasses show similar distribution pattern. The major gas constituents in mud volcano zones

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

    USGS Publications Warehouse

    Bullen, Thomas D.; Chadwick, Oliver A.

    2016-01-01

    Nutrient biolifting is an important pedogenic process in which plant roots obtain inorganic nutrients such as phosphorus (P) and calcium (Ca) from minerals at depth and concentrate those nutrients at the surface. Here we use soil chemistry and stable isotopes of the alkaline earth elements Ca, strontium (Sr) and barium (Ba) to test the hypothesis that biolifting of P has been an important pedogenic process across a soil climosequence developed on volcanic deposits at Kohala Mountain, Hawaii. The geochemical linkage between these elements is revealed as generally positive site-specific relationships in soil mass gains and losses, particularly for P, Ba and Ca, using the ratio of immobile elements titanium and niobium (Ti/Nb) to link individual soil samples to a restricted compositional range of the chemically and isotopically diverse volcanic parent materials. At sites where P is enriched in surface soils relative to abundances in deeper soils, the isotope compositions of exchangeable Ca, Sr and Ba in the shallowest soil horizons (< 10 cm depth) are lighter than those of the volcanic parent materials and trend toward those of plants growing on fresh volcanic deposits. In contrast the isotope composition of exchangeable Ba in deeper soil horizons (> 10 cm depth) at those sites is consistently heavier than the volcanic parent materials. The isotope compositions of exchangeable Ca and Sr trend toward heavier compositions with depth more gradually, reflecting increasing leakiness from these soils in the order Ba < Sr < Ca and downward transfer of light biocycled Ca and Sr to deeper exchange sites. Given the long-term stability of ecosystem properties at the sites where P is enriched in surface soils, a simple box model demonstrates that persistence of isotopically light exchangeable Ca, Sr and Ba in the shallowest soil horizons requires that the uptake flux to plants from those near-surface layers is less than the recycling flux returned to the surface as

  5. Calibration of a conodont apatite-based Ordovician 87Sr/86Sr curve to biostratigraphy and geochronology: Implications for stratigraphic resolution

    USGS Publications Warehouse

    Saltzman, M. R.; Edwards, C. T.; Leslie, S. A.; Dwyer, Gary S.; Bauer, J. A.; Repetski, John E.; Harris, A. G.; Bergstrom, S. M.

    2014-01-01

    The Ordovician 87Sr/86Sr isotope seawater curve is well established and shows a decreasing trend until the mid-Katian. However, uncertainties in calibration of this curve to biostratigraphy and geochronology have made it difficult to determine how the rates of 87Sr/86Sr decrease may have varied, which has implications for both the stratigraphic resolution possible using Sr isotope stratigraphy and efforts to model the effects of Ordovician geologic events. We measured 87Sr/86Sr in conodont apatite in North American Ordovician sections that are well studied for conodont biostratigraphy, primarily in Nevada, Oklahoma, the Appalachian region, and Ohio Valley. Our results indicate that conodont apatite may provide an accurate medium for Sr isotope stratigraphy and strengthen previous reports that point toward a significant increase in the rate of fall in seawater 87Sr/86Sr during the Middle Ordovician Darriwilian Stage. Our 87Sr/86Sr results suggest that Sr isotope stratigraphy will be most useful as a high-resolution tool for global correlation in the mid-Darriwilian to mid-Sandbian, when the maximum rate of fall in 87Sr/86Sr is estimated at ∼5.0–10.0 × 10–5 per m.y. Variable preservation of conodont elements limits the precision for individual stratigraphic horizons. Replicate conodont analyses from the same sample differ by an average of ∼4.0 × 10–5 (the 2σ standard deviation is 6.2 × 10–5), which in the best case scenario allows for subdivision of Ordovician time intervals characterized by the highest rates of fall in 87Sr/86Sr at a maximum resolution of ∼0.5–1.0 m.y. Links between the increased rate of fall in 87Sr/86Sr beginning in the mid-late Darriwilian (Phragmodus polonicus to Pygodus serra conodont zones) and geologic events continue to be investigated, but the coincidence with a long-term rise in sea level (Sauk-Tippecanoe megasequence boundary) and tectonic events (Taconic orogeny) in North America provides a plausible

  6. Mg/Ca, Sr/Ca and Ca isotope ratios in benthonic foraminifers related to test structure, mineralogy and environmental controls

    NASA Astrophysics Data System (ADS)

    Gussone, Nikolaus; Filipsson, Helena L.; Kuhnert, Henning

    2016-01-01

    We analysed Mg/Ca, Sr/Ca and Ca isotope ratios of benthonic foraminifers from sediment core tops retrieved during several research cruises in the Atlantic Ocean, in order to improve the understanding of isotope fractionation and element partitioning resulting from biomineralisation processes and changes in ambient conditions. Species include foraminifers secreting tests composed of hyaline low magnesium calcite, porcelaneous high magnesium calcite as well as aragonite. Our results demonstrate systematic isotope fractionation and element partitioning patterns specific for these foraminiferal groups. Calcium isotope fractionation is similar in porcelaneous and hyaline calcite tests and both groups demonstrate the previously described anomaly with enrichment of heavy isotopes around 3-4 °C (Gussone and Filipsson, 2010). Calcium isotope ratios of the aragonitic species Hoeglundina elegans, on the other hand, are about 0.4‰ lighter compared to the calcitic species, which is in general agreement with stronger fractionation in inorganic aragonite compared to calcite. However, the low and strongly variable Sr content suggests additional processes during test formation, and we propose that transmembrane ion transport or a precursor phase to aragonite may be involved. Porcelaneous tests, composed of high Mg calcite, incorporate higher amounts of Sr compared to hyaline low Mg calcite, in agreement with inorganic calcite systematics, but also porcelaneous tests with reduced Mg/Ca show high Sr/Ca. While calcium isotopes, Sr/Ca and Mg/Ca in benthonic foraminifers primarily appear to fractionate and partition with a dominant inorganic control, δ44/40Ca temperature and growth rate dependencies of benthonic foraminifer tests favour a dominant contribution of light Ca by transmembrane transport relative to unfractionated seawater Ca to the calcifying fluid, thus controlling the formation of foraminiferal δ44/40Ca and Sr/Ca proxy signals.

  7. Nd and Sr isotopic variations in acidic rocks from Japan: significance of upper-mantle heterogeneity

    NASA Astrophysics Data System (ADS)

    Terakado, Yasutaka; Nakamura, Noboru

    1984-10-01

    Initial Nd and Sr isotopic ratios have been measured for Cretaceous acidic and related intermediate rocks (24 volcanic and two plutonic rocks) from the Inner Zone of Southwest Japan (IZSWJ) to investigate the genesis of acidic magmas. The initial Nd and Sr isotopic ratios for these rocks show three interesting features: (1) ɛ Nd values for acidic rocks (+2 to -9) are negatively correlated with ɛ Sr values (+10 to +90) together with those for intermediate rocks ( ɛ Nd=+3 to -8; ɛ Sr=0 to +65). (2) The ɛ Nd values for silica rich rocks (>60% SiO2) correlate with the longitude of the sample locality, decreasing from west to east in a stepwise fashion: Four areas characterized by uniform ɛ Nd values are discriminated. (3) Low silica rocks (<60% SiO2) in a certain area have distinctly different ɛ Nd values from those of the high silica rocks in the same area. These results as well as those deduced from the additional samples collected, for comparison, from other provinces in Japan suggest that the acidic rocks can be formed neither by fractional crystallization processes from more basic magmas nor by crustal assimilation processes. The isotopic variations of the acidic rocks may reflect regional isotopic heterogeneity in the lower crust, and this heterogeneity may ultimately be attributed to the regional heterogeneity of the uppermost-mantle beneath the Japanese Islands.

  8. Ca isotope fractionation and Sr/Ca partitioning associated with anhydrite formation at mid-ocean ridge hydrothermal systems: An experimental approach

    NASA Astrophysics Data System (ADS)

    Syverson, D. D.; Scheuermann, P.; Pester, N. J.; Higgins, J. A.; Seyfried, W. E., Jr.

    2016-12-01

    The elemental and isotopic mass balance of Ca and Sr between seawater and basalt at mid-ocean ridge (MOR) hydrothermal systems is an integrated reflection of the various physiochemical processes, which induce chemical exchange, in the subseafloor. Specifically, the processes of anhydrite precipitation and recrystallization are recognized to be important controls on governing the Ca and Sr elemental and isotope compositions of high temperature vent fluids, however, few experimental data exist to constrain these geochemical effects. Thus, to better understand the associated Sr/Ca partitioning and Ca isotope fractionation and rate of exchange between anhydrite and dissolved constituents, anhydrite precipitation and recrystallization experiments were performed at 175, 250, and 350°C and 500 bar at chemical conditions indicative of active MOR hydrothermal systems. The experimental data suggest that upon entrainment of seawater into MOR hydrothermal systems, anhydrite will precipitate rapidly and discriminate against the heavy isotopes of Ca (Δ44/40Ca(Anh-Fluid) = -0.68 - -0.25 ‰), whereas Sr/Ca partitioning depends on the saturation state of the evolving hydrothermal fluid with respect to anhydrite at each PTX (KD(Anh-Fluid) = 1.24 - 0.55). Coupling experimental constraints with the temperature gradient inferred for high temperature MOR hydrothermal systems in the oceanic crust, data suggest that the Ca isotope and Sr elemental composition of anhydrite formed near the seafloor will be influenced by disequilibrium effects, while, at higher temperatures further into the oceanic crust, anhydrite will be representative of equilibrium Sr/Ca partitioning and Ca isotope fractionation conditions. These experimental observations are consistent with analyzed Sr/Ca and Ca isotope compositions of anhydrites and vent fluids sampled from modern MOR hydrothermal systems1,2 and can be used to further constrain the geochemical effects of hydrothermal circulation in the oceanic crust

  9. Modeling crust-mantle evolution using radiogenic Sr, Nd, and Pb isotope systematics

    NASA Astrophysics Data System (ADS)

    Kumari, Seema; Paul, Debajyoti

    2015-04-01

    The present-day elemental and isotopic composition of Earth's terrestrial reservoirs can be used as geochemical constraints to study evolution of the crust-mantle system. A flexible open system evolutionary model of the Earth, comprising continental crust (CC), upper depleted mantle (UM) -source of mid-ocean ridge basalts (MORB), and lower mantle (LM) reservoir with a D" layer -source of ocean island basalts (OIB), and incorporating key radioactive isotope systematics (Rb-Sr, Sm-Nd, and U-Th-Pb), is solved numerically at 1 Ma time step for 4.55 Ga, the age of the Earth. The best possible solution is the one that produces the present-day concentrations as well as isotopic ratios in terrestrial reservoirs, compiled from published data. Different crustal growth scenarios (exponential, episodic, early and late growth), proposed in earlier studies, and its effect on the evolution of isotope systematics of terrestrial reservoirs is studied. Model simulations strongly favor a layered mantle structure satisfying majority of the isotopic constraints. In the successful model, which is similar to that proposed by Kellogg et al. (1999), the present-day UM comprises of 60% of mantle mass and extends to a depth 1600 km, whereas the LM becomes non-primitive and more enriched than the bulk silicate Earth, mainly due to addition of recycled crustal material. Modeling suggest that isotopic evolution of reservoirs is affected by the mode of crustal growth. Only two scenarios satisfied majority of the Rb-Sr and Sm-Nd isotopic constraints but failed to reproduce the present-day Pb-isotope systematics; exponential growth of crust (mean age, tc=2.3 Ga) and delayed and episodic growth (no growth for initial 900 Ma, tc=2.05 Ga) proposed by Patchett and Arndt (1986). However, assuming a slightly young Earth (4.45 Ga) better satisfies the Pb-isotope systematics. Although, the delayed crustal growth model satisfied Sr-Nd isotopic constraints, presence of early Hadean crust (4.03 and 4.4 Ga

  10. Sea-level and climate forcing of the Sr isotope composition of marginal basins in the late Miocene Mediterranean Basin

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

    Sr isotope records from marginal marine basins track the mixing between sea water and local continental runoff. Because changes in sea level determine the amount of mixing between global marine and continental water, and climate affects the amount of continental runoff, both sea-level and climate changes can potentially be recorded in marine fossil Sr isotope composition. Our 128 new 87Sr/86Sr analyses on 73 oyster, foraminifera, and coral samples from eight late Miocene stratigraphic sections in southern Turkey, Crete, and Sicily show that 87Sr/86Sr in Mediterranean marginal basins started to depart from global ocean values several million years before the Messinian Salinity Crisis (MSC), with sub-basin 87Sr/86Sr commonly dropping 0.000100 below contemporaneous global ocean values. The marked departure coincided with tectonic uplift and basin shallowing along the margins of the Mediterranean Basin. In contrast, centrally-located basins within the Mediterranean (e.g., Cyprus, Sicily, Crete) only record departures during the MSC. Besides this general trend, our 57 new 87Sr/86Sr analyses from the astronomically tuned Lower Evaporite unit deposited during the MSC in the central Apennines (Italy) allow us to explore in detail the effect of sea-level and humidity changes on 87Sr/86Sr . Most of the variation in 87Sr/86Sr that we observe can be explained by changes in eustatic sea level, with greatest departures from global ocean values (with differences up to 0.000150) occurring during sea-level lowstands, which were characterized by relatively arid conditions in the Mediterranean. However, in a few cases, the greatest 87Sr/86Sr departures (up to 0.000300) occur during sea-level highstands, which are marked by more humid conditions. Because the correlations between peaks in Sr departures and highstands (humid conditions) occur only after episodes of prolonged aridity, variations of residence time of continental water (particularly groundwater) could have affected its Sr

  11. Sr isotope zoning in plagioclase from andesites at Cabo De Gata, Spain: Evidence for shallow and deep contamination

    NASA Astrophysics Data System (ADS)

    Waight, Tod E.; Tørnqvist, Jakob B.

    2018-05-01

    Plagioclase crystals in andesites from the Cabo De Gata region show generally radiogenic Sr isotope compositions and consistent core to rim increases in 87Sr/86Sr that are indicative of open system processes in the lithosphere and crustal contamination during crystallization. High-grade metamorphic rocks of the Alpujárride and Nevado-Filábride complexes represent the most likely crustal contaminants. The plagioclases are characterized by subtly zoned and resorbed calcic cores (An73-86). These cores also have radiogenic 87Sr/86Sr (0.7127-0.7129), although typically less radiogenic than plagioclase rims, groundmass plagioclase and whole rock compositions (up to 87Sr/86Sr = 0.7135). These cores are interpreted to represent early crystallization of plagioclase from hydrous melts emplaced into the lower crust. The parental melts to these andesites must therefore have already inherited their radiogenic Sr isotope compositions prior to entering the lower crust and before the onset of crystallization of plagioclase, which is inconsistent with previous models suggesting that the generally radiogenic nature of Sr in these volcanics reflects large amounts of crustal contamination. Instead, the isotope systematics are consistent with models invoked significant addition of a subducted sediment component to the mantle source. The high-An% plagioclase cores are characterized by resorption textures, which are consistent with dissolution during rapid decompression and/or devolatisation during magma migration from the lower crust into upper crustal magma chambers.

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

    PubMed

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

    2014-01-07

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

  13. Pb, Sr, and Nd isotopes in seamount basalts from the Juan de Fuca Ridge and Kodiak-Bowie seamount chain, northeast Pacific

    USGS Publications Warehouse

    Hegner, E.; Tatsumoto, M.

    1989-01-01

    Pb, Sr, and Nd isotopic ratios and their parent/daughter element concentrations for 28 basalts from 10 hotspot and nonhotspot seamounts are reported. Nd and Sr isotopic compositions (143Nd/144Nd = 0.51325-0.51304; 87Sr/86Sr = 0.70237-0.70275) plot in the envelope for Juan de Fuca-Gorda ridge basalts with tholeiitic basalts showing more depleted sources and a better negative correlation than transitional to alkalic basalts. Pb isotopic ratios in tholeiitic and alkalic basalts overlap (206Pb/204Pb = 18.29-19.44) and display a trend toward more radiogenic Pb in alkalic basalts. The isotopic data for hotspot and nonhotspot basalts are indistinguishable and correlate broadly with rock composition, implying that they are controlled by partial melting. The isotopic variation in the seamount basalts is about 60% (Nd-Sr) to 100% (Pb) of that in East Pacific Rise basalts and is interpreted as a lower limit for the magnitude of mantle heterogeneity in the northeast Pacific. The data indicate absence of a chemically distinct plume component in the linear seamount chains and strongly suggest an origin from mid-ocean ridge basalt-like east Pacific mantle. -Authors

  14. Nd, Pb, Sr, and O isotopic characterization of Saudi Arabian Shield terranes

    USGS Publications Warehouse

    Stoeser, D.B.; Frost, C.D.

    2006-01-01

    New Nd, Sr and O isotopic data for granitoid rocks of the Saudi Arabian Shield are presented together with published Nd, Pb, Sr and O isotopic data and all available geologic and geochronologic information to re-evaluate the terranes defined for the Saudi Arabian part of the Arabian-Nubian Shield. Three groups of terranes are identified: 1) the western arc terranes, 2) the eastern arc terranes, and 3) the Khida terrane. The Khida terrane is the only terrane composed of pre-Neoproterozoic continental crust. The western arc terranes are of oceanic arc affinity, and have the least radiogenic Pb and Sr and most radiogenic Nd isotopic compositions and some of the lowest ??18O values of any rocks of the Saudi Arabian Shield. Although some previous studies have characterized the eastern arc terranes as of continental affinity, this study shows that they too are composed of Neoproterozoic oceanic arcs, although their sources have slightly elevated 208Pb/204Pb, Nd, Sri, and ??18O values compared to the western arc terranes. These data suggest that either the isotopic composition of the mantle source for the western arc terranes is more depleted than that of the eastern arc terranes or the eastern arc terranes have been mixed with a small amount of cratonic source material, or both. We further elaborate on the Hulayfah-Ad Dafinah fault zone as a major boundary within the Saudi Arabian portion of the East African Orogen. With further study, its northern extension may be shown to pass through what has been defined as the Hail terrane, and its southern extension appears to lie under cover east of the Tathlith-Malahah terrane and extend into Yemen. It may represent the collision zone between East and West Gondwana, and at the very least it is an important suture between groups of arc terranes of contrasting isotopic composition caught between two converging continents.

  15. Sr-Nd-Hf Isotopic Analysis of <10 mg Dust Samples: Implications for Ice Core Dust Source Fingerprinting

    NASA Astrophysics Data System (ADS)

    Újvári, Gábor; Wegner, Wencke; Klötzli, Urs; Horschinegg, Monika; Hippler, Dorothee

    2018-01-01

    Combined Sr-Nd-Hf isotopic data of two reference materials (AGV-1/BCR2) and 50, 10, and 5 mg aliquots of carbonate-free fine grain (<10 μm) separates of three loess samples (Central Europe/NUS, China/BEI, USA/JUD) are presented. Good agreement between measured and reference Sr-Nd-Hf isotopic compositions (ICs) demonstrate that robust isotopic ratios can be obtained from 5 to 10 mg size rock samples using the ion exchange/mass spectrometry techniques applied. While 87Sr/86Sr ratios of dust aluminosilicate fractions are affected by even small changes in pretreatments, Nd isotopic ratios are found to be insensitive to acid leaching, grain-size or weathering effects. However, the Nd isotopic tracer is sometimes inconclusive in dust source fingerprinting (BEI and NUS both close to ɛNd(0) -10). Hafnium isotopic values (<10 μm fractions) are homogenous for NUS, while highly variable for BEI. This heterogeneity and vertical arrays of Hf isotopic data suggest zircon depletion effects toward the clay fractions (<2 μm). Monte Carlo simulations demonstrate that the Hf IC of the dust <10 μm fraction is influenced by both the abundance of zircons present and maturity of crustal rocks supplying this heavy mineral, while the <2 μm fraction is almost unaffected. Thus, ɛHf(0) variations in the clay fraction are largely controlled by the Hf IC of clays/heavy minerals having high Lu/Hf and radiogenic 176Hf/177Hf IC. Future work should be focused on Hf IC of both the <10 and <2 μm fractions of dust from potential source areas to gain more insight into the origin of last glacial dust in Greenland ice cores.

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

    USGS Publications Warehouse

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

    2004-01-01

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

  17. Sm-Nd and Initial Sr-87/Sr-86 Isotopic Systematics of Asuka 881394 and Cumulate Eucrites Yamato 980318/433 Compared

    NASA Technical Reports Server (NTRS)

    Nyquist, L. E.; Shih, C-Y; Young, Y. D.; Takeda, H.

    2011-01-01

    The Asuka 881394 achondrite contains fossil Al-26 and Mn-53 and has a Pb-206/Pb-207 age of 4566.5 +/- 0.2 Ma, the oldest for an achondrite. Recent re-investigation of A881394 yielded revised initial Sm-146/Sm-144 = (9.1 +/- 1.4) x 10(exp -3), a Sm-147-Nd-143 age of 4525 +/- 58 Ma, a Rb-87-Sr-87 age of 4490 +/- 130 Ma, and initial Sr-87/Sr-86 = 0.698991 +/- 19, respectively. The relatively large uncertainties in the Sm-Nd and Rb-Sr ages are due to disturbances of the isotopic systematics of tridymite and other minor phases. A preliminary value for the Sm-147-Nd-143 age of the Yamato 980318 cumulate eucrite of 4560 +/- 150 Ma was refined in later work to 4567 +/- 24 Ma as reported orally at LPSC 35. Similarly, a preliminary value for Sm-146/Sm-144 = (7.7 +/- 1.2) x 10 (exp -3) was refined to (6.0 +/- 0.3) x 10(exp -3). For Yamato 980433, a Sm-147-Nd-143 age of 4542 +/-42 Ma and Sm-146/Sm-144 = (5.7 +/- 0.5) x 10(exp -3) has been reported. Because these two cumulate eucrites are paired, we consider them to represent one igneous rock and present their combined isotopic data here.

  18. Chemical and Sr isotopic characterization of North America uranium ores: Nuclear forensic applications

    DOE PAGES

    Balboni, Enrica; Jones, Nina; Spano, Tyler; ...

    2016-08-31

    This study reports major, minor, and trace element data and Sr isotope ratios for 11 uranium ore (uraninite, UO 2+x) samples and one processed uranium ore concentrate (UOC) from various U.S. deposits. The uraninite investigated represent ores formed via different modes of mineralization (e.g., high- and low-temperature) and within various geological contexts, which include magmatic pegmatites, metamorphic rocks, sandstone-hosted, and roll front deposits. In situ trace element data obtained by laser ablation-ICP-MS and bulk sample Sr isotopic ratios for uraninite samples investigated here indicate distinct signatures that are highly dependent on the mode of mineralization and host rock geology. Relativemore » to their high-temperature counterparts, low-temperature uranium ores record high U/Th ratios (>1000), low total rare earth element (REE) abundances (<1 wt%), high contents (>300 ppm) of first row transition metals (Sc, Ti, V, Cr, Mn, Co, Ni), and radiogenic 87Sr/ 86Sr ratios (>0.7200). Comparison of chondrite normalized REE patterns between uraninite and corresponding processed UOC from the same locality indicates identical patterns at different absolute concentrations. Lastly, this result ultimately confirms the importance of establishing geochemical signatures of raw, uranium ore materials for attribution purposes in the forensic analysis of intercepted nuclear materials.« less

  19. Chemical and Sr isotopic characterization of North America uranium ores: Nuclear forensic applications

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Balboni, Enrica; Jones, Nina; Spano, Tyler

    This study reports major, minor, and trace element data and Sr isotope ratios for 11 uranium ore (uraninite, UO 2+x) samples and one processed uranium ore concentrate (UOC) from various U.S. deposits. The uraninite investigated represent ores formed via different modes of mineralization (e.g., high- and low-temperature) and within various geological contexts, which include magmatic pegmatites, metamorphic rocks, sandstone-hosted, and roll front deposits. In situ trace element data obtained by laser ablation-ICP-MS and bulk sample Sr isotopic ratios for uraninite samples investigated here indicate distinct signatures that are highly dependent on the mode of mineralization and host rock geology. Relativemore » to their high-temperature counterparts, low-temperature uranium ores record high U/Th ratios (>1000), low total rare earth element (REE) abundances (<1 wt%), high contents (>300 ppm) of first row transition metals (Sc, Ti, V, Cr, Mn, Co, Ni), and radiogenic 87Sr/ 86Sr ratios (>0.7200). Comparison of chondrite normalized REE patterns between uraninite and corresponding processed UOC from the same locality indicates identical patterns at different absolute concentrations. Lastly, this result ultimately confirms the importance of establishing geochemical signatures of raw, uranium ore materials for attribution purposes in the forensic analysis of intercepted nuclear materials.« less

  20. The combined use of 87Sr/86Sr and carbon and water isotopes to study the hydrochemical interaction between groundwater and lakewater in mantled karst

    USGS Publications Warehouse

    Katz, B.G.; Bullen, T.D.

    1996-01-01

    The hydrochemical interaction between groundwater and lakewater influences the composition of water that percolates downward from the surficial aquifer system through the underlying intermediate confining unit and recharges the Upper Floridan aquifer along highlands in Florida. The 87Sr/86Sr ratio along with the stable isotopes, D, 18O, and 13C were used as tracers to study the interaction between groundwater, lakewater, and aquifer minerals near Lake Barco, a seepage lake in the mantled karst terrane of northern Florida. Upgradient from the lake, the 87Sr/86Sr ratio of groundwater decreases with depth (mean values of 0.71004, 0.70890, and 0.70852 for water from the surficial aquifer system, intermediate confining unit, and Upper Floridan aquifer, respectively), resulting from the interaction of dilute oxygenated recharge water with aquifer minerals that are less radiogenic with depth. The concentrations of Sr2+ generally increase with depth, and higher concentrations of Sr2+ in water from the Upper Floridan aquifer (20-35 ??g/L), relative to water from the surficial aquifer system and the intermediate confining unit, result from the dissolution of Sr-bearing calcite and dolomite in the Eocene limestone. Dissolution of calcite [??13C = -1.6 permil (???)] is also indicated by an enriched ??13CDIC (-8.8 to - 11.4???) in water from the Upper Floridan aquifer, relative to the overlying hydrogeologic units (??13CDIC < - 16???). Groundwater downgradient from Lake Barco was enriched in 18O and D relative to groundwater upgradient from the lake, indicating mixing of lakewater leakage and groundwater. Downgradient from the lake, the 87Sr/86Sr ratio of groundwater and aquifer material become less radiogenic and the Sr2+ concentrations generally increase with depth. However, Sr2+ concentrations are substantially less than in upgradient groundwaters at similar depths. The lower Sr2+ concentrations result from the influence of anoxic lakewater leakage on the mobility of Sr2

  1. The combined use of 87Sr/86Sr and carbon and water isotopes to study the hydrochemical interaction between groundwater and lakewater in mantled karst

    NASA Astrophysics Data System (ADS)

    Katz, Brian G.; Bullen, Thomas D.

    1996-12-01

    The hydrochemical interaction between groundwater and lakewater influences the composition of water that percolates downward from the surficial aquifer system through the underlying intermediate confining unit and recharges the Upper Floridan aquifer along highlands in Florida. The 87Sr/86Sr ratio along with the stable isotopes, D, 18O, and 13C were used as tracers to study the interaction between groundwater, lakewater, and aquifer minerals near Lake Barco, a seepage lake in the mantled karst terrane of northern Florida. Upgradient from the lake, the 87Sr/86Sr ratio of groundwater decreases with depth (mean values of 0.71004, 0.70890, and 0.70852 for water from the surficial aquifer system, intermediate confining unit, and Upper Floridan aquifer, respectively), resulting from the interaction of dilute oxygenated recharge water with aquifer minerals that are less radiogenic with depth. The concentrations of Sr2+ generally increase with depth, and higher concentrations of Sr2+ in water from the Upper Floridan aquifer (20-35 μg/L), relative to water from the surficial aquifer system and the intermediate confining unit, result from the dissolution of Sr-bearing calcite and dolomite in the Eocene limestone. Dissolution of calcite [δ13C= -1.6permil(‰)] is also indicated by an enriched δ13CDIC(-8.8 to -11.4 ‰) in water from the Upper Floridan aquifer, relative to the overlying hydrogeologic units (δ13CDIC< -16‰). Groundwater downgradient from Lake Barco was enriched in18O and D relative to groundwater upgradient from the lake, indicating mixing of lakewater leakage and groundwater. Downgradient from the lake, the 87Sr/86Sr ratio of groundwater and aquifer material become less radiogenic and the Sr2+ concentrations generally increase with depth. However, Sr2+ concentrations are substantially less than in upgradient groundwaters at similar depths. The lower Sr2+ concentrations result from the influence of anoxic lakewater leakage on the mobility of Sr2+ from

  2. The size-isotopic evolution connection among layered mafic instrusions: Clues from a Sr-Nd isotopic study of a small complex

    NASA Astrophysics Data System (ADS)

    Poitrasson, Franck; Pin, Christian; Duthou, Jean-Louis; Platevoet, Bernard

    1994-05-01

    Several theoretical and experimental works have focused on the processes occuring in continental mafic magma chambers. In contrast, systematic isotopic studies of natural remnants of these latter remain scarce, although they can give fundamental constraints for theoretical studies. This is especially true if different layered complex with contrasting characteristics (e.g., different size) are compared. For this reason, we present the results of a Sr-Nd isotopic profile across a small layered mafic intrusion of Permian age exposed near Fozzano (SW Corsica). In the main zone of the layered section, decreasing Sr-87/Sr(sub i)-86 and increasing Nd-143/Nd(sub i)-144 are observed from less evolved (bottom) to more evolved (top) rocks. This peculiar pattern precludes assimilation and fractional crystallization (AFC) as a dominant mechanism in the petrogenesis of this body. Instead, we interpret this trend as reflecting the dilution of an early stage contaminated magma by several reinjections of fresh basalt in the chamber. In agreement with mineralogical and structural data, every cyclic unit is interpreted as a new magmatic input. On the basis of rough refill and fractional crystallization (RFC) calculations, the average volume for each reinjection is estimated to have been about 0.04 cu km. The cumulative volume of these injections would amount to about 75% of the total volume of the layered complex. This implies that reinjections were accompanied by an important increase of the volume of the chamber or by magma withdrawal by surface eruptions. The RFC mechanism documented within this small layered body constrasts with the isotopic pattern observed between several intrusions at the regional scale in SW Corsica, and within large continental mafic magma chambers elsewhere. In these cases the isotopic evolution is dominated by AFC processes, and there is no clear isotopic evidence for reinjections, unless major influx of fresh magma occurred. It is suggested that there is

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

    USGS Publications Warehouse

    Duffield, W.A.; Ruiz, J.

    1998-01-01

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

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

    PubMed

    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.

  5. S- and Sr-isotopic compositions in barite-silica chimney from the Franklin Seamount, Woodlark Basin, Papua New Guinea: constraints on genesis and temporal variability of hydrothermal fluid

    NASA Astrophysics Data System (ADS)

    Ray, Durbar; Banerjee, Ranadip; Balakrishnan, S.; Paropkari, Anil L.; Mukhopadhyay, Subir

    2017-07-01

    Isotopic ratios of strontium and sulfur in six layers across a horizontal section of a hydrothermal barite-silica chimney from Franklin Seamount of western Woodlark Basin have been investigated. Sr-isotopic ratios in barite samples (87Sr/86Sr = 0.70478-0.70493) are less radiogenic than seawater (87Sr/86Sr = 0.70917) indicating that substantial leaching of sub-seafloor magma was involved in the genesis of hydrothermal fluid. The SO2 of magma likely contributed a considerable amount of lighter S-isotope in fluid and responsible for the formation of barite, which is isotopically lighter (δ34S = 19.4-20.5 ‰) than modern seawater (δ34S 21 ‰). The systematic changes in isotopic compositions across the chimney wall suggest temporal changes in the mode of mineral formation during the growth of the chimney. Enrichment of heavy S- and Sr-isotopes (δ34S = 20.58 ‰; 87Sr/86Sr = 0.70493) in the outermost periphery of the chimney indicates that, at the initial stage of chimney development, there was a significant contribution of seawater sulfate during barite mineralization. Thereafter, thickening of chimney wall occurred due to precipitation of fluid carrying more magmatic components relative to seawater. This led to a gradual enrichment of lighter isotopes (δ34S = 20.42-19.48 ‰; 87Sr/86Sr = 0.70491-0.704787) toward the inner portion of the chimney wall. In contrast, the innermost layer surrounding the fluid conduit is characterized by heavier and more radiogenic isotopes (δ34S = 20.3 ‰; 87Sr/86Sr = 0.7049). This suggests there was increasing influence of percolating seawater on the mineral paragenesis at the waning phase of the chimney development.

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

    USGS Publications Warehouse

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

    2011-01-01

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

  7. Characterizing multiple sources and interaction in the critical zone through Sr-isotope tracing of surface and groundwater

    NASA Astrophysics Data System (ADS)

    Negrel, Philippe; Pauwels, Hélène

    2017-04-01

    The Critical Zone (CZ) is the lithosphere-atmosphere boundary where complex physical, chemical and biological processes occurs and control the transfer and storage of water and chemical elements. This is the place where life-sustaining resources are, where nutrients are being released from the rocks. Because it is the place where we are living, this is a fragile zone, a critical zone as a perturbed natural ecosystem. Water resources in hard-rocks commonly involve different hydrogeological compartments such as overlying sediments, weathered rock, the weathered-fissured zone, and fractured bedrock. Streams, lakes and wetlands that drain such environments can drain groundwater, recharge groundwater, or do both. Groundwater resources in many countries are increasingly threatened by growing demand, wasteful use, and contamination. Surface water and shallow groundwater are particularly vulnerable to pollution, while deeper resources are more protected from contamination. Here, we first report on Sr isotope data as well as major ions, from shallow and deep groundwater in several granite and schist areas over France with intensive agriculture covering large parts of these catchments. In three granite and Brioverian 'schist' areas of the Armorican Massif, the range in Sr contents in groundwater from different catchments agrees with previous work on groundwater sampled from granites in France. The Sr content is well correlated with Mg and both are partly related to agricultural practices and water rock interaction. The relationship between Sr- isotope and Mg/Sr ratios allow defining the different end-members, mainly rain, agricultural practice and water-rock interaction. The data from the Armorican Massif and other surface and groundwater for catchment draining silicate bedrocks (300-450Ma) like the Hérault, Seine, Moselle, Garonne, Morvan, Margeride, Cantal, Pyrénées and Vosges are scattered between at least three geochemical signatures. These include fertilizer and

  8. Mixed fluid sources involved in diamond growth constrained by Sr-Nd-Pb-C-N isotopes and trace elements

    NASA Astrophysics Data System (ADS)

    Klein-BenDavid, Ofra; Pearson, D. Graham; Nowell, Geoff M.; Ottley, Chris; McNeill, John C. R.; Cartigny, Pierre

    2010-01-01

    Sub-micrometer inclusions in diamonds carry high-density fluids (HDF) from which the host diamonds have precipitated. The chemistry of these fluids is our best opportunity of characterizing the diamond-forming environment. The trace element patterns of diamond fluids vary within a limited range and are similar to those of carbonatitic/kimberlitic melts that originate from beneath the lithospheric mantle. A convecting mantle origin for the fluid is also implied by C isotopic compositions and by a preliminary Sr isotopic study (Akagi, T., Masuda, A., 1988. Isotopic and elemental evidence for a relationship between kimberlite and Zaire cubic diamonds. Nature 336, 665-667.). Nevertheless, the major element chemistry of HDFs is very different from that of kimberlites and carbonatites, varying widely and being characterized by extreme K enrichment (up to ˜ 39 wt.% on a water and carbonate free basis) and high volatile contents. The broad spectrum of major element compositions in diamond-forming fluids has been related to fluid-rock interaction and to immiscibility processes. Elemental signatures can be easily modified by a variety of mantle processes whereas radiogenic isotopes give a clear fingerprint of the time-integrated evolution of the fluid source region. Here we present the results of the first multi radiogenic-isotope (Sr, Nd, Pb) and trace element study on fluid-rich diamonds, implemented using a newly developed off-line laser sampling technique. The data are combined with N and C isotope analysis of the diamond matrix to better understand the possible sources of fluid involved in the formation of these diamonds. Sr isotope ratios vary significantly within single diamonds. The highly varied but unsupported Sr isotope ratios cannot be explained by immiscibility processes or fluid-mineral elemental fractionations occurring at the time of diamond growth. Our results demonstrate the clear involvement of a mixed fluid, with one component originating from ancient

  9. Tracking selenium behaviour in chalk aquifer (northern France): Sr and 34S-sulphates isotopes constraints.

    NASA Astrophysics Data System (ADS)

    Cary, Lise; Benabderraziq, Hind; Elkhattabi, Jamal; Parmentier, Marc; Gourcy, Laurence; Négrel, Philippe

    2014-05-01

    Groundwaters in parts of the Paris Basin (France) are facing increasing selenium (Se) contents that can exceed the drinking water limit of 10 μg/L according to the European Framework Directive in the field of water policy (2000/60/EC). To better understand the groundwater origins and the selenium dynamics, the water chemistry of the Chalk aquifer supplying drinkable water to Lille city was studied. This area is submitted to quantitative and qualitative pressure from industrial, urban and agriculture origins. An integrated study was settled to determine the water sources and dynamics of elements, with a focus on Se. After a large chemical characterisation of the groundwater chemistry in the four field wells, a monthly monitoring was held in four wells and in the Deûle channel. Chemical analysis of major and trace elements, stable isotopes (δ18O, δ2H), strontium isotopes, and δ34S and δ18O of sulphates were realised. The chemical composition of solids sampled at various depths at vicinity of the four wells was also analysed. The specific geochemical signature of groundwater as revealed by Sr isotopes, in addition to element concentrations ratios like Mg/Sr and Se/Sr, highlighted mixture of three main groundwaters bodies: (1) the upstream groundwaters in the recharge area with the most radiogenic 87Sr/86Sr isotopic signature; (2) the confined groundwaters with high Sr concentrations due to water-rock interactions and the lowest 87Sr/86Sr isotopic signature close to the one of the chalk in Paris and London basins; (3) the Se-rich formations of Tertiary and Quaternary. The contents of Se, mainly present as SeV I (and locally as SeIV ), displayed spatial and temporal disparities that can be explained by geological and hydrogeological conditions. Se-rich clayed sediments originating from the dismantling of Se-rich tertiary formations (i.e. Ypresian) overlay the chalk formation and can be found in saturated conditions depending of the water table level. Oxidation of

  10. Correlated study of initial Sr-87/Sr-86 and Al-Mg isotopic systematics and petrologic properties in a suite of refractory inclusions from the Allende meteorite

    NASA Technical Reports Server (NTRS)

    Podosek, Frank A.; Zinner, Ernst K.; Lundberg, Laura L.; Brannon, Joyce C.; Macpherson, Glenn J.

    1991-01-01

    The abundance and the distribution of Al-26, and the initial Sr-87/Sr-86 ratios were determined in a suite of six coarse-grained Ca-Al-rich inclusions from the Allende meteorite, using, respectively, petrographic and chemical characterizations and ion-probe mass spectrometric analyses of the Al-Mg isotopic system, and thermal emission spectrometric analyses of the Rb-Sr system. Results establish a firm association between primitive Al-26/Al-27 and primitive Sr-87/Sr-86 found in each of these inclusions. None of the results required interpretation in terms of heterogeneously distributed Al-26.

  11. High-precision 87Sr/86Sr analyses in wines and their use as a geological fingerprint for tracing geographic provenance.

    PubMed

    Marchionni, Sara; Braschi, Eleonora; Tommasini, Simone; Bollati, Andrea; Cifelli, Francesca; Mulinacci, Nadia; Mattei, Massimo; Conticelli, Sandro

    2013-07-17

    The radiogenic isotopic compositions of inorganic heavy elements such as Sr, Nd, and Pb of the food chain may constitute a reliable geographic fingerprint, their isotopic ratios being inherited by the geological substratum of the territory of production. The Sr isotope composition of geomaterials (i.e., rocks and soils) is largely variable, and it depends upon the age of the rocks and their nature (e.g., genesis, composition). In this study we developed a high-precision analytical procedure for determining Sr isotopes in wines at comparable uncertainty levels of geological data. With the aim of verifying the possibility of using Sr isotope in wine as a reliable tracer for geographic provenance, we performed Sr isotope analyses of 45 bottled wines from four different geographical localities of the Italian peninsula. Their Sr isotope composition has been compared with that of rocks from the substrata (i.e., rocks) of their vineyards. In addition wines from the same winemaker but different vintage years have been analyzed to verify the constancy with time of the (87)Sr/(86)Sr. Sr isotope compositions have been determined by solid source thermal ionization mass spectrometry following purification of Sr in a clean laboratory. (87)Sr/(86)Sr of the analyzed wines is correlated with the isotopic values of the geological substratum of the vineyards, showing little or no variation within the same vineyard and among different vintages. Large (87)Sr/(86)Sr variation is observed among wines from the different geographical areas, reinforcing the link with the geological substratum of the production territory. This makes Sr isotopes a robust geochemical tool for tracing the geographic authenticity and provenance of wine.

  12. The Sr isotope chemostratigraphy as a tool for solving stratigraphic problems of the Upper Proterozoic (Riphean and Vendian)

    NASA Astrophysics Data System (ADS)

    Kuznetsov, A. B.; Semikhatov, M. A.; Gorokhov, I. M.

    2014-11-01

    Published and original data on the Sr isotopic characterization of carbonates from the Riphean and Vendian key sections of the Southern Urals, Siberia, Asia, Africa, Australia, and North America are considered in compliance with the suggested principles of reconstructing the Sr isotopic composition of the Proterozoic seawater. The suggested methodic approach is used to plot the reference curve of the 87Sr/86Sr variations in the Riphean and Vendian oceans. During the time span of 1600-1250 Ma, the 87Sr/86Sr variations were in a narrow range corresponding to 0.70456-0.70494, but approaching the date of about 1030 Ma, the 87Sr/86Sr ratio rose to 0.70601-0.70611 and then quickly declined to 0.70519-0.70523 near the date of 1000 Ma. In the second half of the late Riphean and in the Vendian, the ratio grew almost steadily from 0.70521-0.70535 to values of 0.70874-0.70885 characteristic of the Late Vendian time. The subsequent regular growth of that ratio in seawater lasted from 840 to 550 Ma, though there were short-term epochs when the ratio noticeably dropped to 0.70561-0.70575 at approximately 760 Ma and to 0.70533-0.70538 at 670-660 Ma. After the mid-Late Vendian maximum, it declined to 0.70812-0.70823 at the end of the Nemakit-Daldynian Age and decreased to 0.70806-0.70812 during the Tommotian Age of the Early Cambrian. As is shown, the Sr isotopic variations in the Riphean and Vendian oceans were interrelated with global tectonic events in geospheres and formation stages of the Rodinia and Gondwana supercontinents. The Baikalian Complex of Siberia is considered in the work as a case in point illustrating advantages of the expounded approach with respect to age substantiation of particular stratigraphic subdivisions.

  13. Application of Sr and O isotope relations to the petrogenesis of the alkaline rocks of the Red Hill complex, New Hampshire, USA

    USGS Publications Warehouse

    Foland, K.A.; Friedman, I.

    1977-01-01

    The Red Hill ring complex in central New Hampshire is composed of apparently cogenetic syenites, nepheline-sodalite syenite, and granite. The ages and petrogenetic relations among five of the six recognized units have been investigated by rubidiumstrontium and oxygen isotope analysis of whole rocks and separated minerals. Whole-rock samples from three syenite units are consistent with a single Rb-Sr isochron which gives an age of 198??3 m.y. and an initial (87Sr/86Sr)o ratio of 0.70330??0.00016 (??2 sigma; ??=1.42?? 10-11y-1). However, Sr isotope data for two other units, nepheline syenite and granite, are not consistent with this isochron but rather indicate higher initial ratios which range from 0.7033 to about 0.707. Whole-rock O isotope analyses give ??18O values which range from+6.2 to+9.3??? Sr and O isotope analyses on mineral separates indicate that observed whole-rock variations in (87Sr/86Sr)o are primary and are not due to any secondary process. The fact that the isotope systematics correlate with rock type, suggests that crustal interaction is likely to have played a significant role in the development of this over-and undersaturated association. Such process(es), while still not fully delineated, could be of fundamental importance to the genesis of associations of critically undersaturated and oversaturated intrusives. The data support the idea that interaction between magmas and crustal materials strongly influenced the compositional relations of similar complexes elsewhere including those of the White Mountain magma series. ?? 1977 Springer-Verlag.

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

    NASA Astrophysics Data System (ADS)

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

    2016-03-01

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

  15. Evaluation strategies and uncertainty calculation of isotope amount ratios measured by MC ICP-MS on the example of Sr.

    PubMed

    Horsky, Monika; Irrgeher, Johanna; Prohaska, Thomas

    2016-01-01

    This paper critically reviews the state-of-the-art of isotope amount ratio measurements by solution-based multi-collector inductively coupled plasma mass spectrometry (MC ICP-MS) and presents guidelines for corresponding data reduction strategies and uncertainty assessments based on the example of n((87)Sr)/n((86)Sr) isotope ratios. This ratio shows variation attributable to natural radiogenic processes and mass-dependent fractionation. The applied calibration strategies can display these differences. In addition, a proper statement of uncertainty of measurement, including all relevant influence quantities, is a metrological prerequisite. A detailed instructive procedure for the calculation of combined uncertainties is presented for Sr isotope amount ratios using three different strategies of correction for instrumental isotopic fractionation (IIF): traditional internal correction, standard-sample bracketing, and a combination of both, using Zr as internal standard. Uncertainties are quantified by means of a Kragten spreadsheet approach, including the consideration of correlations between individual input parameters to the model equation. The resulting uncertainties are compared with uncertainties obtained from the partial derivatives approach and Monte Carlo propagation of distributions. We obtain relative expanded uncertainties (U rel; k = 2) of n((87)Sr)/n((86)Sr) of < 0.03 %, when normalization values are not propagated. A comprehensive propagation, including certified values and the internal normalization ratio in nature, increases relative expanded uncertainties by about factor two and the correction for IIF becomes the major contributor.

  16. He and Sr isotopic constraints on subduction contributions to Woodlark Basin volcanism, Solomon Islands

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Trull, T.W.; Kurz, M.D.; Perfit, M.R.

    In order to assess the nature and spatial extent of subduction contributions to arc volcanism, Sr and He isotopic compositions are measured for dredged volcanic rocks from the Woodlark Basin in the western Pacific. {sup 87}Sr/{sup 86}Sr ratios increase geographically, from ocean ridge values (.7025-.7029) at the Woodlark Spreading Center to island arc ratios (.7035-.7039) in the Solomon Islands forearc, with intermediate values near the triple junction where the Woodlark Spreading Center subducts beneath the Solomon Islands. {sup 3}He/{sup 4}He ratios are also more radiogenic in the forearc (6.9 {plus minus} .2 R{sub a} at active Kavachi volcano) than alongmore » the spreading center, where values typical of major ocean ridges were found (8.2 - 9.3 R{sub a}). Very low {sup 3}He/{sup 4}He ratios occur in many triple junction rocks (.1 to 5 R{sub a}), but consideration of He isotopic differences between crushing and melting analyses suggests that the low ratios were caused by atmospheric (1 R{sub a}) and radiogenic ({approx} 0.2 R{sub a}) helium addition after eruption. Variations in unaltered, magnetic {sup 3}He/{sup 4}He, and {sup 87}Sr/{sup 86}Sr ratios are best explained by subduction-related fluid or silicate melt contributions to the magma source region, perhaps from ancient Pacific lithosphere. However, mantle volatiles dominate the generation of Woodlark Basin rocks despite extensive subduction in the region.« less

  17. Application of {sup 87}Sr/{sup 86}Sr, {delta}{sup 18}O and {delta}{sup 13}C Isotopes to diagenesis, correlation and connectivity of a fractured chalk reservoir, the Sidi El Kilani Field Tunisia

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Mearns, E.W.; Mcbride, J.J.; Bramwell, M.

    1995-08-01

    Strontium Stratigraphy Analysis of the primary matrix chalk of the Abiod Formation reservoir in the Sidi El Kilani Field indicate a Campanian to Maastrichtian age (Upper Cretaceous). A resolution of {+-}1Ma has been achieved and results suggest that there are no major stratigraphic breaks in the studied sequences. Sr-O-C isotope data from early fracture-filling calcite cements suggest they may have formed by the redistribution of CaCO{sub 3} from underlying carbonate sequences and may have precipitated at temperatures in the region of 35-55{degrees}C. The {sup 87}Sr/{sup 86}Sr isotope ratios of formation waters determined by residual salt analysis (SrRSA) suggest that themore » chemical evolution of waters during reservoir filling was controlled by the influx of basinal waters as opposed to in situ water-rock interaction. Late, fracture-filling dolomite and barite cements have Sr-O-C isotope characteristics consistent with precipitation from these migrating basinal fluids at temperatures similar to current reservoir conditions (70-75{degrees}C). Sr RSA results suggest that the reservoir section in two of the wells may have been in direct lateral communication at the time of oil emplacement. These wells however are separated by a strike-slip fault. The SrRSA results therefore suggest that the fault is a partial barrier which has restricted pressure equilibration in the relatively short timescale of oil production, but which may have allowed homogenization of Sr isotope ratios in formation water.« less

  18. Ca and Sr Isotope Sytematics in Mid-Ocean Ridge Hydrothermal Fluids

    NASA Astrophysics Data System (ADS)

    Pester, N. J.; Syverson, D. D.; Higgins, J. A.; Seyfried, W. E., Jr.

    2016-12-01

    We report a comprehensive suite of Ca isotopic data (δ44/40Ca) from mid-ocean ridge hydrothermal fluids, standardized relative to seawater. Samples were acquired from 7 different vent fields on the EPR, JdFR and MAR during expeditions between 1999 and 2014. All endmember hydrothermal fluids (within analytical uncertainty) reflect an entirely MORB-dominated signal (-1.0 to -1.2 ‰). This rather uniform signal, despite variable fluid chemistries and a mixture of mafic to ultramafic host lithologies, is somewhat surprising given the noteworthy Ca concentrations in both the hydrothermal fluids and precursor seawater. One explanation for this observation involves the change in anhydrite (CaSO4) saturation with increasing temperature, and the molal concentration ratio of [Mg]:[Ca]:[SO4] in modern seawater of 53:10:28. The near quantitative removal of seawater Mg to silicate alteration phases, favorable at all temperatures, is largely charge balanced by exchange for basaltic Ca, and this process alone can account for the majority of the rock dominated δ44/40Casw signal. That these values are equivalent to MORB, however, suggests a high proportion of this Mg-Ca exchange occurs after seawater Ca precipitates as anhydrite in lower temperature (recharge) regimes of the hydrothermal system, aided by the low [Ca]/[SO4]. 87/86Sr ratios of hydrothermal fluids exhibit a seawater signal of 20 to 30% and Sr is therefore not quantitatively removed during incipient anhydrite formation. Strontium mobility in hydrothermal systems is still poorly understood, but the offset between the Ca and Sr isotopic signatures is consistent with near-equilibrium partitioning of Sr into anhydrite observed in recent experiments. Such observations from modern MOR systems place important constraints on the role of hydrothermal fluxes in paleo-seawater evolution, such as feedbacks involving significant variability in [Mg]:[Ca]:[SO4] ratios of seawater suggested over much of the Phanerozoic.

  19. Advances in Multicollector ICPMS for precise and accurate isotope ratio measurements of Uranium isotopes

    NASA Astrophysics Data System (ADS)

    Bouman, C.; Lloyd, N. S.; Schwieters, J.

    2011-12-01

    The accurate and precise determination of uranium isotopes is challenging, because of the large dynamic range posed by the U isotope abundances and the limited available sample material. Various mass spectrometric techniques are used for the measurement of U isotopes, where TIMS is the most accepted and accurate one. Multicollector inductively coupled plasma mass spectrometry (MC-ICPMS) can offer higher productivity compared to TIMS, but is traditionally limited by low efficiency of sample utilisation. This contribution will discuss progress in MC-ICPMS for detecting 234U, 235U, 236U and 238U in various uranium reference materials from IRMM and NBL. The Thermo Scientific NEPTUNE Plus with Jet Interface offers a modified dry plasma ICP interface using a large interface pump combined with a special set of sample and skimmer cones giving ultimate sensitivity for all elements across the mass range. For uranium, an ion yield of > 3 % was reported previously [1]. The NEPTUNE Plus also offers Multi Ion Counting using discrete dynode electron multipliers as well as two high abundance-sensitivity filters to discriminate against peak tailing effects on 234U and 236U originating from the major uranium beams. These improvements in sensitivity and dynamic range allow accurate measurements of 234U, 235U and 236U abundances on very small samples and at low concentration. In our approach, minor U isotopes 234U and 236U were detected on ion counters with high abundance sensitivity filters, whereas 235U and 238U were detected on Faraday Cups using a high gain current amplifier (10e12 Ohm) for 235U. Precisions and accuracies for 234U and 236U were down to ~1%. For 235U, subpermil levels were reached.

  20. Sr isotope characterization of atmospheric inputs to soils along a climate gradient of the Chilean Coastal Range

    NASA Astrophysics Data System (ADS)

    Oeser, Ralf; Schuessler, Jan A.; Floor, Geerke H.; von Blanckenburg, Friedhelm

    2017-04-01

    The rate and degree of rock weathering controls the release, distribution, and cycling of mineral nutrients at the Earth's surface, being essential for developing and sustaining of ecosystems. Climate plays an important role as water flow and temperature determine both the biological community and activity, and also set the speed of weathering. Because of this double control by climate, the impact of biological activity on rock weathering and the feedbacks between the geosphere and the biosphere under different climatic conditions are not well understood. We explore the impact of biota on rock weathering in the four EarthShape primary study areas which are situated along the Chilean Coastal Range, featuring an outstanding vegetation gradient controlled by climate, ranging over 2000 km from hyper-arid, to temperate, to humid conditions. The study sites are within 80 km of the Pacific coast and are located in granitic lithology. Moreover, the sites were unglaciated during the last glacial maximum. However, as substrates get depleted in mineral nutrients, ecosystems are increasingly nourished by atmospheric inputs, sources, such as solutes contained in rain, dust, and volcanic ash. We aim to quantify the primary nutrient inputs to the ecosystem from these different potential sources. Radiogenic strontium (Sr) isotope ratios are a powerful tool to trace chemical weathering, soil formation, as well as cation provenance and mobility [1]. We determined 87Sr/86Sr ratios on bulk bedrock, saprolite, and soil and performed sequential extractions of the the easily bioavailable soil phases up to 2 m depth on two soil depth profiles in each of the four study sites. Our first results from the La Campana study site indicate that the radiogenic Sr isotope ratios of saprolite samples decrease from 0.70571 (n = 4) at the base of the profile to lower values of 0.70520 (n = 4) at the top of the immobile saprolite, indicating increasing biotite weathering. 87Sr/86Sr increases in the

  1. Using Nd and Sr isotopes to trace dust and volcanic inputs to soils on French Guadeloupe Island

    NASA Astrophysics Data System (ADS)

    Guo, J.; Pereyra, Y.; Ma, L.; Gaillardet, J.; Sak, P. B.; Bouchez, J.

    2017-12-01

    Soil is at the central part of the Critical Zone for its important roles in sustaining ecosystems and agriculture. At French Guadeloupe, a tropical humid volcanic island, previous studies have shown that the mineral nutrient elements such as K, Na, Ca, and Mg are highly depleted in the surface soil. And mineral nutrients introduced by dusts are an important mineral nutrient source for vegetation growth in this area. It is important to understand and quantify the sources of the mineral dust added to surface soils. Nd isotope ratios, due to their distinct signatures between two unique end-members in soils for this area: the young volcanic areas like Guadeloupe and the dust source region from the old continental shields like Sahara Desert, can be a robust tracer to understand this critical process. Nevertheless, Sr isotope ratios can trace the inputs of marine aerosols. Here we present a new Nd isotope study on Guadeloupe soil depth profiles, combined with previous Sr isotope data, to fingerprint the sources of dust and volcanic inputs into soils. Soil samples from three surface profiles (0 - 1000cm deep) at different locations of the Guadeloupe Island were systematically analyzed. The results show distinct depth variations for Nd isotope signature along profiles. For all profiles, deep soils are relatively consisted with bedrock value (ɛNd: 5.05). But in surface soils (0-600cm), unlike Sr isotope ratios that are significantly modified by marine aerosol input, Nd isotope ratios show similar decrease (to ɛNd:-10) and frequent fluctuations toward the surface, suggesting dust is the dominant source of Nd in these soils. This conclusion is further supported by REE and other trace element data. Thus, with a simplified two end-member model, Sahara dust contributes the Nd percentages in soils varying from 10.7% at the deepest profiles to 69.5% on surface, showing a significant amount of Nd on the surface soil came from dust source. The deep soil profiles are also

  2. Multi-isotope tracers to investigate processes in the Elbe, Weser and Ems river catchment using B, Mo, Sr, and Pb isotope ratios assessed by MC ICP-MS

    NASA Astrophysics Data System (ADS)

    Irrgeher, Johanna; Reese, Anna; Zimmermann, Tristan; Prohaska, Thomas; Retzmann, Anika; Wieser, Michael E.; Zitek, Andreas; Proefrock, Daniel

    2017-04-01

    Environmental monitoring of complex ecosystems requires reliable sensitive techniques based on sound analytical strategies to identify the source, fate and sink of elements and matter. Isotopic signatures can serve to trace pathways by making use of specific isotopic fingermarks or to distinguish between natural and anthropogenic sources. The presented work shows the potential of using the isotopic variation of Sr, Pb (as well-established isotopic systems), Mo and B (as novel isotopic system) assessed by MC ICP-MS in water and sediment samples to study aquatic ecosystem transport processes. The isotopic variation of Sr, Pb, Mo and B was determined in different marine and estuarine compartments covering the catchment of the German Wadden Sea and its main tributaries, the Elbe, Weser and Ems River. The varying elemental concentrations, the complex matrix and the expected small variations in the isotopic composition required the development and application of reliable analytical measurement approaches as well as suited metrological data evaluation strategies. Aquatic isoscapes were created using ArcGIS® by relating spatial isotopic data with geographical and geological maps. The elemental and isotopic distribution maps show large variation for different parameters and also reflect the numerous impact factors (e.g. geology, anthropogenic sources) influencing the catchment area.

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

    NASA Astrophysics Data System (ADS)

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

    2012-03-01

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

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

    NASA Astrophysics Data System (ADS)

    Li, Y.; Jiang, S.

    2015-12-01

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

  5. Sr and Nd isotope composition of the metamorphic, sedimentary and ultramafic xenoliths of Lanzarote (Canary Islands): Implications for magma sources

    NASA Astrophysics Data System (ADS)

    Aparicio, Alfredo; Tassinari, Colombo C. G.; García, Roberto; Araña, Vicente

    2010-01-01

    The lavas produced by the Timanfaya eruption of 1730-1736 (Lanzarote, Canary Islands) contain a great many sedimentary and metamorphic (metasedimentary), and mafic and ultramafic plutonic xenoliths. Among the metamorphosed carbonate rocks (calc-silicate rocks [CSRs]) are monomineral rocks with forsterite or wollastonite, as well as rocks containing olivine ± orthopyroxene ± clinopyroxene ± plagioclase; their mineralogical compositions are identical to those of the mafic (gabbros) and ultramafic (dunite, wherlite and lherzolite) xenoliths. The 87Sr/ 86Sr (around 0.703) and 143Nd/ 144Nd (around 0.512) isotope ratios of the ultramafic and metasedimentary xenoliths are similar, while the 147Sm/ 144Nd ratios show crustal values (0.13-0.16) in the ultramafic xenoliths and mantle values (0.18-0.25) in some CSRs. The apparent isotopic anomaly of the metamorphic xenoliths can be explained in terms of the heat source (basaltic intrusion) inducing strong isotopic exchange ( 87Sr/ 86Sr and 143Nd/ 144Nd) between metasedimentary and basaltic rocks. Petrofabric analysis also showed a possible relationship between the ultramafic and metamorphic xenoliths.

  6. Improvements in Precise and Accurate Isotope Ratio Determination via LA-MC-ICP-MS by Application of an Alternative Data Reduction Protocol

    NASA Astrophysics Data System (ADS)

    Fietzke, J.; Liebetrau, V.; Guenther, D.; Frische, M.; Zumholz, K.; Hansteen, T. H.; Eisenhauer, A.

    2008-12-01

    An alternative approach for the evaluation of isotope ratio data using LA-MC-ICP-MS will be presented. In contrast to previously applied methods it is based on the simultaneous responses of all analyte isotopes of interest and the relevant interferences without performing a conventional background correction. Significant improvements in precision and accuracy can be achieved when applying this new method and will be discussed based on the results of two first methodical applications: a) radiogenic and stable Sr isotopes in carbonates b) stable chlorine isotopes of pyrohydrolytic extracts. In carbonates an external reproducibility of the 87Sr/86Sr ratios of about 19 ppm (RSD) was achieved, an improvement of about a factor of 5. For recent and sub-recent marine carbonates a mean radiogenic strontium isotope ratio 87Sr/86Sr of 0.709170±0.000007 (2SE) was determined, which agrees well with the value of 0.7091741±0.0000024 (2SE) reported for modern sea water [1,2]. Stable chlorine isotope ratios were determined ablating pyrohydrolytic extracts with a reproducibility of about 0.05‰ (RSD). For basaltic reference material JB1a and JB2 chlorine isotope ratios were determined relative to SMOC (standard mean ocean chlorinity) δ37ClJB-1a = (-0.99±0.06) ‰ and δ37ClJB-1a = (-0.60±0.03) ‰ (SD), respectively, in accordance with published data [3]. The described strategies for data reduction are considered to be generally applicable for all isotope ratio measurements using LA-MC-ICP-MS. [1] J.M. McArthur, D. Rio, F. Massari, D. Castradori, T.R. Bailey, M. Thirlwall, S. Houghton, Palaeogeo. Palaeoclim. Palaeoeco., 2006, 242 (126), doi: 10.1016/j.palaeo.2006.06.004 [2] J. Fietzke, V. Liebetrau, D. Guenther, K. Guers, K. Hametner, K. Zumholz, T.H. Hansteen and A. Eisenhauer, J. Anal. At. Spectrom., 2008, 23, 955-961, doi:10.1039/B717706B [3] J. Fietzke, M. Frische, T.H. Hansteen and A. Eisenhauer, J. Anal. At. Spectrom., 2008, 23, 769-772, doi:10.1039/B718597A

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

    NASA Astrophysics Data System (ADS)

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

    2014-10-01

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

  8. Ages and Nd, Sr isotopic systematics in the Sierran foothills ophiolite belt, CA: the Smartville and Feather River complexes

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Shaw, H.F.; Niemeyer, S.

    1985-01-01

    Sm-Nd dating has shown the Kings-Kaweah ophiolite to be approx. 480 My old. Its Nd, Sr, and Pb isotopic compositions require an unusually old depleted mantle source. Samples from the Smartville and Feather River complexes have been analyzed in a search for similar highly depleted, early Paleozoic ophiolites in the northern foothills ophiolite belt. Six whole rocks from Smartville, encompassing representative lithologies, plus plagioclase and pyroxene mineral separates define a 183 +/- 22 My Sm-Nd isochron. This age, interpreted as the igneous age, is older than, but within error of, approx. 160 My U-Pb ages previously obtained from plagiogranite zirconmore » analyses. One diabase with unusually high Rb/Sr yields a depleted mantle Sr model age of 200 +/- 25 My, consistent with the Sm-ND age. These compositions are clearly oceanic in character but do not discriminate among possible tectonic settings for the formation of the Smartville complex. Sm-Nd data for flaser gabbros and related rocks from Feather River scatter about an approx. 230 My errorchron with element of/sub Nd/(T) = +6.3 to +8.7. Initial /sup 87/Sr//sup 86/Sr ranges from 0.7028 to 0.7031. These results indicate a complex history with initial isotopic heterogeneities and/or disturbances of the isotopic systems. If primary, the element of/sub Nd/ (T) values are somewhat low, suggesting a possible arc origin for these rocks. Neither the Smartville nor Feather R. complexes appear to be related to the Kings-Kaweah ophiolite which, so far, is unique among foothill ophiolites in having an early Paleozoic age and a clear MORB, as opposed to arc or marginal basin, isotopic signature.« less

  9. Reconstruction of travel history using coupled δ18 O and 87 Sr/86 Sr measurements of hair.

    PubMed

    Chau, Thuan H; Tipple, Brett J; Hu, Lihai; Fernandez, Diego P; Cerling, Thure E; Ehleringer, James R; Chesson, Lesley A

    2017-03-30

    Oxygen isotope ratios (δ 18 O values) of hair largely reflect features of regional hydrology while strontium isotope ratios ( 87 Sr/ 86 Sr) are thought to reflect bedrock geology; combination of both isotope signatures may provide greater capacity for determining provenance and reconstructing travel history of an organism. To test this hypothesis, we compared the O-Sr isotope profiles of hair from domestic horses with known residency histories. Tail hairs were collected from a pair of horses pastured together for a period of 16 months, one of which lived in a different location for the 8 months prior. Hair samples were washed with solvents to remove external contaminants prior to sequential sampling for δ 18 O and 87 Sr/ 86 Sr analysis via TC/EA-IRMS and MC-ICP-MS, respectively. Hair digests were concentrated and analyzed employing low-flow natural aspiration to measure 87 Sr/ 86 Sr. Tail hair from the control and transported horses had mean δ 18 O values of 11.25 ± 1.62 ‰ and 10.96 ± 1.53 ‰, and mean 87 Sr/ 86 Sr of 0.7101 ± 0.0006 and 0.7109 ± 0.0020, respectively. The δ 18 O and 87 Sr/ 86 Sr profiles for the control and transported horses were indistinguishable when they were pastured together. The 87 Sr/ 86 Sr profiles were significantly different during the period that the horses were living apart, while the δ 18 O values were indistinguishable during that period. By comparing the O-Sr isotope profiles of a control and transported horse, we investigated isotopic signal(s) potentially useful for reconstructing travel histories via high-resolution sequential sampling along single strands of tail hair. Improved analytical capabilities allowed for extremely low Sr abundance samples to be analyzed for 87 Sr/ 86 Sr and proved capable of resolving a horse's movement between distinct regions. Copyright © 2017 John Wiley & Sons, Ltd. Copyright © 2017 John Wiley & Sons, Ltd.

  10. Interaction between different groundwaters in brittany catchments (france): characterizing multiple sources through Sr- and S isotope tracing

    NASA Astrophysics Data System (ADS)

    Negrel, Ph; Pauwels, H.

    2003-04-01

    Water resources in hard-rocks commonly involve different hydrogeological compartments such as overlying sediments, weathered rock, the weathered-fissured zone, and fractured bedrock. Streams, lakes and wetlands that drain such environments can drain groundwater, recharge groundwater, or do both. Groundwater resources in many countries are increasingly threatened by growing demand, wasteful use, and contamination. Surface water and shallow groundwater are particularly vulnerable to pollution, while deeper resources are more protected from contamination. Sr- and S-isotope data as well as major ions, from shallow and deep groundwater in three granite and Brioverian "schist" areas of the Armorican Massif (NW France) with intensive agriculture covering large parts are presented. The stable-isotope signatures of the waters plot close to the general meteoric-water line, reflecting a meteoric origin and the lack of significant evaporation or water-rock interaction. The water chemistry from the different catchments shows large variation in the major-element contents. Plotting Na, Mg, NO_3, K, SO_4 and Sr vs. Cl contents concentrations reflect agricultural input from hog and livestock farming and fertilizer applications, with local sewage-effluent influence, although some water samples are clearly unpolluted. The δ34S(SO_4) is controlled by several potential sources (atmospheric sulphate, pyrite-derived sulphates, fertilizer sulphates). Some δ18O and δ34S values are expected to increase through sulphate reduction, with higher effect on δ34S for the dissimilatory processes and on δ18O for assimilatory processes. The range in Sr contents in groundwater from different catchments agrees with previous work on groundwater sampled from granites in France. The Sr content is well correlated with Mg and both are related to agricultural practises. As in granite-gneiss watersheds in France, 87Sr/86Sr ratios range from 0.71265 to 0.72009. The relationship between 87Sr/86Sr and Mg/Sr

  11. Bayesian Integration of Isotope Ratio for Geographic Sourcing of Castor Beans

    PubMed Central

    Webb-Robertson, Bobbie-Jo; Kreuzer, Helen; Hart, Garret; Ehleringer, James; West, Jason; Gill, Gary; Duckworth, Douglas

    2012-01-01

    Recent years have seen an increase in the forensic interest associated with the poison ricin, which is extracted from the seeds of the Ricinus communis plant. Both light element (C, N, O, and H) and strontium (Sr) isotope ratios have previously been used to associate organic material with geographic regions of origin. We present a Bayesian integration methodology that can more accurately predict the region of origin for a castor bean than individual models developed independently for light element stable isotopes or Sr isotope ratios. Our results demonstrate a clear improvement in the ability to correctly classify regions based on the integrated model with a class accuracy of 60.9 ± 2.1% versus 55.9 ± 2.1% and 40.2 ± 1.8% for the light element and strontium (Sr) isotope ratios, respectively. In addition, we show graphically the strengths and weaknesses of each dataset in respect to class prediction and how the integration of these datasets strengthens the overall model. PMID:22919270

  12. Sr isotope variations in the Carnian-Norian succession at Pizzo Mondello, Sicani Mountains, Sicily

    NASA Astrophysics Data System (ADS)

    Onoue, T.; Yamashita, K.; Rigo, M.; Abate, B.

    2017-12-01

    The Norian stage in the Late Triassic is exceptionally long (23 Myr) and was subdivided into three substages: the Lacian, Alaunian, and Sevatian. In order to infer the Norian environmental changes in the western Tethys Ocean, the stratigraphic variations of 87Sr/86Sr in the Upper Triassic limestone succession in Sicily were examined. The Pizzo Mondello section studied here mainly consists of a pelagic carbonate sequence of the Scillato Formation, and ranges in age from Tuvalian (late Carnian) to Rhaetian. The Scillato Formation represents a deep-water pelagic facies deposited along the Sicanian Basin in the western Tethys Ocean. We selected fine-grained limestone samples from both the microfacies of lime-mudstone and wackestone to approximate the primary 87Sr/86Sr signature of the limestone beds. The 87Sr/86Sr values are relatively constant in the Tuvalian and Lacian (early Norian). However, the remarkable rise in 87Sr/86Sr occurred across the Lacian-Alaunian (early-middle Norian) transition. Variations in 87Sr/86Sr values show an increasing trend in 87Sr/86Sr from 0.7077 at the base of Lacian to 0.7080 in the Sevatian (late Norian). In the Sevatian, the 87Sr/86Sr ratios display a sudden negative excursion toward lower values and show a relatively quick recovery to pre-excursion 87Sr/86Sr ratios. Korte et al. (2003) suggested that the rise in the 87Sr/86Sr values from the middle Carnian to the late Norian coincide with the Cimmerian orogeny. Our new 87Sr/86Sr data from the Pizzo Mondello section reveal a comparable trend, with a sharp increase in 87Sr/86Sr within the Alaunian, suggesting the rapid uplift and erosion in the Cimmerian Mountains at this time. The cause of the 87Sr/86Sr excursion in the Sevatian remains uncertain. However, the biostratigraphic record of conodonts suggests that a morphological evolution towards platform-less elements occurred with the beginning of the Sr-isotope excursion.

  13. Precise and accurate isotope ratio measurements by ICP-MS.

    PubMed

    Becker, J S; Dietze, H J

    2000-09-01

    The precise and accurate determination of isotope ratios by inductively coupled plasma mass spectrometry (ICP-MS) and laser ablation ICP-MS (LA-ICP-MS) is important for quite different application fields (e.g. for isotope ratio measurements of stable isotopes in nature, especially for the investigation of isotope variation in nature or age dating, for determining isotope ratios of radiogenic elements in the nuclear industry, quality assurance of fuel material, for reprocessing plants, nuclear material accounting and radioactive waste control, for tracer experiments using stable isotopes or long-lived radionuclides in biological or medical studies). Thermal ionization mass spectrometry (TIMS), which used to be the dominant analytical technique for precise isotope ratio measurements, is being increasingly replaced for isotope ratio measurements by ICP-MS due to its excellent sensitivity, precision and good accuracy. Instrumental progress in ICP-MS was achieved by the introduction of the collision cell interface in order to dissociate many disturbing argon-based molecular ions, thermalize the ions and neutralize the disturbing argon ions of plasma gas (Ar+). The application of the collision cell in ICP-QMS results in a higher ion transmission, improved sensitivity and better precision of isotope ratio measurements compared to quadrupole ICP-MS without the collision cell [e.g., for 235U/238U approximately 1 (10 microg x L(-1) uranium) 0.07% relative standard deviation (RSD) vs. 0.2% RSD in short-term measurements (n = 5)]. A significant instrumental improvement for ICP-MS is the multicollector device (MC-ICP-MS) in order to obtain a better precision of isotope ratio measurements (with a precision of up to 0.002%, RSD). CE- and HPLC-ICP-MS are used for the separation of isobaric interferences of long-lived radionuclides and stable isotopes by determination of spallation nuclide abundances in an irradiated tantalum target.

  14. Investigating the hydrological significance of stalagmite geochemistry (Mg, Sr) using Sr isotope and particulate element records across the Late Glacial-to-Holocene transition

    NASA Astrophysics Data System (ADS)

    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

  15. Accurate and precise determination of isotopic ratios by MC-ICP-MS: a review.

    PubMed

    Yang, Lu

    2009-01-01

    For many decades the accurate and precise determination of isotope ratios has remained a very strong interest to many researchers due to its important applications in earth, environmental, biological, archeological, and medical sciences. Traditionally, thermal ionization mass spectrometry (TIMS) has been the technique of choice for achieving the highest accuracy and precision. However, recent developments in multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) have brought a new dimension to this field. In addition to its simple and robust sample introduction, high sample throughput, and high mass resolution, the flat-topped peaks generated by this technique provide for accurate and precise determination of isotope ratios with precision reaching 0.001%, comparable to that achieved with TIMS. These features, in combination with the ability of the ICP source to ionize nearly all elements in the periodic table, have resulted in an increased use of MC-ICP-MS for such measurements in various sample matrices. To determine accurate and precise isotope ratios with MC-ICP-MS, utmost care must be exercised during sample preparation, optimization of the instrument, and mass bias corrections. Unfortunately, there are inconsistencies and errors evident in many MC-ICP-MS publications, including errors in mass bias correction models. This review examines "state-of-the-art" methodologies presented in the literature for achievement of precise and accurate determinations of isotope ratios by MC-ICP-MS. Some general rules for such accurate and precise measurements are suggested, and calculations of combined uncertainty of the data using a few common mass bias correction models are outlined.

  16. Sr-Nd-Pb Isotope Geochemistry of Melange Formation: Implications for Identification of Fluid Sources in the Mantle Wedge and the Arc

    NASA Astrophysics Data System (ADS)

    Bebout, G. E.; King, R. L.; Moriguti, T.; Nakamura, E.

    2004-12-01

    Paramount to our ability to decipher the behavior of fluids and melts within the mantle wedge and the overall subduction system are the chemical compositions of rocks adjacent to the slab-mantle interface. Profound metamorphic and metasomatic alteration of pre-subduction lithologies to form melange along the slab-mantle interface may yield rock types inheriting mixed chemical compositions of diverse pre-subduction lithologies. Early work on melange geochemistry indicates competitive effects between mechanical mixing, metasomatism by fluids or melts, and mineral stabilities imposed by the resulting bulk composition. We have explored the Sr-Nd-Pb isotope geochemistry of low- to high-grade melange zones in the Catalina Schist, CA, to address this crucial missing component in studies of subduction-zone mass flux. The Catalina Schist contains lawsonite-albite (LA), lawsonite-blueschist (LB), and amphibolite (AM) facies melange zones, all with mineralogy dominated by talc, chlorite, and Na-Ca amphiboles, with additional minerals such as micas, rutile, zircon, and apatite stabilized based on bulk sample chemistry. Major element compositions vary, from strongly ultramafic in the AM melange, to more crustal-like compositions (i.e., more reminiscent of basaltic to sedimentary protoliths) for LA and LB melange. However, initial Sr and Nd isotope ratios for all grades of melange are essentially indistinguishable, displaying a wide variation from 87Sr/86Sr=0.703-0.709 and ɛ Nd= +15 to -15. Covariations are generally negative, similar to that of the mantle array, but with some samples extending to higher Sr ratios at constant ɛ Nd that probably reflect inheritance of seawater Sr. No clear mixing relationships between 87Sr/86Sr and 1/Sr exist, suggesting either localized buffering of Sr isotope ratios or that mixing relations are obscured by secondary devolatilization. However, a clear mixing trend for Nd indicates two end-members, one a high-concentration, positive ɛ Nd

  17. A multi-proxy isotope study (δ41K, δ26Mg, 87Sr/86Sr) of low-temperature oceanic crust alteration: the Troodos Ophiolite and Ocean Drilling Program Hole 801C

    NASA Astrophysics Data System (ADS)

    Santiago Ramos, D. P.; Higgins, J. A.

    2017-12-01

    Low-temperature alteration of oceanic crust plays an important role in a number of geochemical cycles, thus modulating the chemical composition of the oceans. In particular, it has been established that low-temperature (<150oC) alteration of basalt is a major sink of seawater potassium. However, little is known about the effects of this process on the potassium isotope composition of seawater, which is 0.5‰ enriched relative to bulk silicate Earth (δ41KBSE=-0.54‰). Here we measure a number of isotope systems (δ41K, δ26Mg, 87Sr/86Sr) in both host rock and vein material from the upper volcanic section of Cretaceous (Troodos Ophiolite) and Jurassic (ODP 801C) oceanic crust using a MC-ICP-MS. The goal is to estimate the K isotopic fractionation associated with basalt alteration in low-temperature conditions, and how it might affect the K isotope enrichment of seawater relative to BSE. We find that marine hydrothermal samples from Troodos and ODP site 801C are enriched in potassium relative to the unaltered glass compositions and have δ41K values both higher and lower than BSE, ranging from -0.45‰ to -0.69‰ (n = 9) and -0.32‰ to -0.71‰ (n = 5), respectively. The low measured δ41K values could represent 1) fractionation (α<1) of K isotopes during uptake from seawater (δ41KSW 0‰), or 2) remobilized mantle-sourced K (δ41KBSE=-0.54‰) from deeper within the ophiolite sequence. Measurements of δ26Mg (n=15) and 87Sr/86Sr (n=12) in these samples yield enriched values relative to bulk silicate Earth, suggesting that alteration of oceanic crust likely happened under high water-to-rock ratios in both Troodos and ODP 801C, and that the added potassium is seawater-sourced. We thus suggest that the isotopically light δ41K values measured in both sites are associated with the formation of secondary clays enriched in the 39K isotope. This light isotope enrichment could be intensified if seawater K sourcing is a diffusion-limited process, as aqueous potassium

  18. Ca, Sr, O and D isotope approach to defining the chemical evolution of hydrothermal fluids: example from Long Valley, CA, USA

    USGS Publications Warehouse

    Brown, Shaun T.; Kennedy, B. Mack; DePaolo, Donald J.; Hurwitz, Shaul; Evans, William C.

    2013-01-01

    We present chemical and isotopic data for fluids, minerals and rocks from the Long Valley meteoric-hydrothermal system. The samples encompass the presumed hydrothermal upwelling zone in the west moat of the caldera, the Casa Diablo geothermal field, and a series of wells defining a nearly linear, ∼16 km long, west-to-east trend along the likely fluid flow path. Fluid samples were analyzed for the isotopes of water, Sr, and Ca, the concentrations of major cations and anions, alkalinity, and total CO2. Water isotope data conform to trends documented in earlier studies, interpreted as indicating a single hydrothermal fluid mixing with local groundwater. Sr isotopes show subtle changes along the flow path, which requires rapid fluid flow and minimal reaction between the channelized fluids and the wallrocks. Sr and O isotopes are used to calculate fracture spacing using a dual porosity model. Calculated fracture spacing and temperature data for hydrothermal fluids indicate the system is (approximately) at steady-state. Correlated variations among total CO2, and the concentration and isotopic composition of Ca suggest progressive fluid degassing (loss of CO2), which drives calcite precipitation as the fluid flows west-to-east and cools. The shifts in Ca isotopes require that calcite precipitated at temperatures of 150–180 °C is fractionated by ca. −0.3‰ to −0.5‰ relative to aqueous species. Our data are the first evidence that Ca isotopes undergo kinetic fractionation at high temperatures (>100 °C) and can be used to trace calcite precipitation along hydrothermal fluid flow paths.

  19. Strontium isotope ratios (87Sr/86Sr) of tooth enamel: a comparison of solution and laser ablation multicollector inductively coupled plasma mass spectrometry methods.

    PubMed

    Copeland, Sandi R; Sponheimer, Matt; le Roux, Petrus J; Grimes, Vaughan; Lee-Thorp, Julia A; de Ruiter, Darryl J; Richards, Michael P

    2008-10-01

    Strontium isotope ratios (87Sr/86Sr) in tooth enamel provide a means to investigate migration and landscape use in humans and other animals. Established methods for measuring (87)Sr/(86)Sr in teeth use bulk sampling (5-20 mg) and labor-intensive elemental purification procedures before analysis by either thermal ionization mass spectrometry (TIMS) or multicollector inductively coupled plasma mass spectrometry (MC-ICP-MS). Another method for measuring 87Sr/86Sr is laser ablation MC-ICP-MS, but concerns have been expressed about its accuracy for measuring tooth enamel. In this study we test the precision and accuracy of the technique by analyzing 30 modern rodent teeth from the Sterkfontein Valley, South Africa by laser ablation MC-ICP-MS and solution MC-ICP-MS. The results show a mean difference in 87Sr/86Sr measured by laser ablation and by solution of 0.0003 +/- 0.0002. This degree of precision is well within the margin necessary for investigating the potential geographic origins of humans or animals in many areas of the world. Because laser ablation is faster, less expensive, and less destructive than bulk sampling solution methods, it opens the possibility for conducting 87Sr/86Sr analyses of intra-tooth samples and small and/or rare specimens such as micromammal and fossil teeth.

  20. Tracing Nile sediment sources by Sr and Nd isotope signatures (Uganda, Ethiopia, Sudan)

    NASA Astrophysics Data System (ADS)

    Padoan, Marta; Garzanti, Eduardo; Harlavan, Yehudit; Villa, Igor Maria

    2011-06-01

    Strontium and neodymium isotopes, measured on diverse mud and sand fractions of sediment in transit along all major Nile branches, identify detritus sourced from Precambrian basements, Mesozoic strata, and Tertiary volcanic rocks exposed along the shoulders of the East African rift and in Ethiopian highlands. Sr and Nd isotopic ratios reflect the weighted average of detrital components generated in different catchments, allowing us to discriminate provenance, calculate sediment budgets, and investigate grain-size and hydraulic-sorting effects. 87Sr/ 86Sr and 143Nd/ 144Nd range, respectively, from as high as 0.722 and as low as 0.5108 for sediment derived from Archean gneisses in northern Uganda, to 0.705 and 0.5127 for sediment derived from Neoproterozoic Ethiopian and Eritrean basements. 87Sr/ 86Sr and 143Nd/ 144Nd, ranging 0.705-0.709 and 0.5124-0.5130 for Blue Nile tributaries, are 0.704-0.705 and 0.5127-0.5128 for largely volcaniclastic sediments of River Tekeze-Atbara, and 0.705-0.706 and 0.5126-0.5127 for main Nile sediments upstream Lake Nasser. Model mantle derivation ages ( tDM), oldest in Uganda where sediment is principally derived from the Congo Craton (3.4-3.0 Ga for Victoria and Albert Nile), progressively decrease northward across the Saharan Metacraton, from 2.6 Ga (Bahr el Jebel in South Sudan), to 2.4-2.2 Ga (Bahr ez Zeraf across the Sudd), and finally 1.6-1.3 Ga (White Nile upstream Khartoum). Instead, tDM ages of Sobat mud increase from 0.9 to 1.5 Ga across the Machar marshes. TDM ages are younger for sediments shed by Ethiopian (1.2-0.7 Ga) and Eritrean basements (1.5-1.2 Ga), and youngest for sediments shed from Ethiopian flood basalts (0.3-0.2 Ga). Integrated geochemical, mineralogical, and settling-equivalence analyses suggest influence on the Nd isotopic signal by volcanic lithic grains and titanite rather than by LREE-rich monazite or allanite. Because contributions by ultradense minerals is subordinate, intrasample variability of Sr and

  1. Constraints on Martian Differentiation Processes from Rb-Sr and Sm-Nd Isotopic Analyses of the Basaltic Shergottite QUE 94201

    NASA Technical Reports Server (NTRS)

    Borg, Lars E.; Nyquist, Larry E.; Taylor, Larry A.; Wiesmann, Henry; Shih, Chi-Y.

    1997-01-01

    Isotopic analyses of mineral, leachate, and whole rock fractions from the Martian shergottite meteorite QUE 94201 yield Rb-Sr and Sm-Nd crystallization ages of 327 +/- 12 and 327 +/- 19 Ma, respectively. These ages are concordant, although the isochrons are defined by different fractions within the meteorite. Comparison of isotope dilution Sm and Nd data for the various QUE 94201 fractions with in situ ion microprobe data for QUE 94201 minerals from the literature demonstrate the presence of a leachable crustal component in the meteorite. This component is likely to have been added to QUE 94201 by secondary alteration processes on Mars, and can affect the isochrons by selectively altering the isotopic systematics of the leachates and some of the mineral fractions. The absence of crustal recycling processes on Mars may preserve the geochemical evidence for early differentiation and the decoupling of the Rb-Sr and Sm-Nd isotopic systems, underscoring one of the fundamental differences between geologic processes on Mars and the Earth.

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

    USGS Publications Warehouse

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

    1992-01-01

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

  3. Generation and Evolution of Quaternary Magmas Beneath Tengchong: Sr-Nd-Pb-Hf Isotope and Zircon U-series Age Constraints

    NASA Astrophysics Data System (ADS)

    Zou, H.; Ma, M.; Fan, Q.; Xu, B.; Li, S. Q.; Zhao, Y.; King, D. T., Jr.

    2017-12-01

    The Tengchong volcanic field on the southeastern margin of the Tibetan Plateau represents rare Quaternary volcanic eruptions on the plateau. The Quaternary Tengchong volcanic field formed high-potassium calc-alkaline volcanic rocks that include trachybasalts, basaltic trachyandesites, trachyandesites, and dacites. Herein, we present comprehensive Nd-Sr-Pb-Hf isotopic and elemental data for trachybasalts, basaltic trachyandesites, and trachyandesites from four young Tengchong volcanoes at Maanshan, Dayingshan, Heikongshan, and Laoguipo, in order to understand their magma genesis and evolution. Nd-Sr-Pb-Hf isotopes for the primitive Tengchong magma (trachybasalts with SiO2 <52.5 wt. % and MgO >5.5% wt. %) reflect a heterogeneous enriched mantle source. High Th/U, Th/Ta, and Rb/Nb ratios and Nd-Sr-Pb-Hf isotope characteristics of the primitive magmas suggest that the enriched mantle beneath Tengchong formed as a result of subduction of clay-rich sediments, which probably came from the Indian continental plate. Partial melting of the enriched mantle was generated by deep continental subduction coupled with recent regional extension in the Tengchong area. With regard to the evolved magmas (basaltic trachyandesites and trachyandesites), good correlations between SiO2 content and the ratios 87Sr/86Sr, 143Nd/144Nd, 206Pb/204Pb, and 177Hf/176Hf strongly suggest that the combined assimilation and fractional crystallization (AFC) was an important process during magma evolution to form these basaltic trachyandesites and trachyandesites. Uranium-series zircon dating on these evolved lavas from Tengchong is used to constrain their magma evolution and residence timescales.

  4. Rb-Sr Isotopic Studies Of Antarctic Lherzolitic Shergottite Yamato 984028

    NASA Technical Reports Server (NTRS)

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

    2009-01-01

    Yamato 984028 is a Martian meteorite found in the Yamato Mountains of Antarctica. It is classified as a lherzolitic shergottite and petrographically resembles several other lherzolitic shergottites, i.e. ALHA 77005, LEW 88516, Y-793605 and Y-000027/47/97 [e.g. 2-5]. These meteorites have similarly young crystallization ages (152-185 Ma) as enriched basaltic shergottites (157-203 Ma), but have very different ejection ages (approximately 4 Ma vs. approximately 2.5 Ma), thus they came from different martian target crater areas. Lherzolitic shergottites have mg-values approximately 0.70 and represent the most mafic olivine-pyroxene cumulates. Their parental magmas were melts derived probably from the primitive Martian mantle. Here we present Rb-Sr isotopic data for Y-984028 and compare these data with those obtained from other lherzolitic and olivine-phyric basaltic shergottites to better understand the isotopic characteristics of their primitive mantle source regions. Corresponding Sm-Nd analyses for Y-984028 are in progress.

  5. The Nd-, Sr- and Pb-isotopic character of lavas from Taal, Laguna de Bay and Arayat volcanoes, southwestern Luzon, Philippines: Implications for arc magma petrogenesis

    USGS Publications Warehouse

    Mukasa, S.B.; Flower, M.F.J.; Miklius, Asta

    1994-01-01

    Following the amalgamation of a collage of pre-Neogene terranes largely by strike-slip and convergence mechanisms to form the Philippine islands, volcanic chains, related to oppositely dipping subduction zones, developed along the eastern and western margins of the archipelago. There is ample field evidence that this volcanic activity, predominantly calc-alkaline in chemical character, had commenced by the Oligocene. Volcanoes resulting from subduction along the Manila-Negros trench in the west (e.g. Taal, Laguna de Bay and Arayat) form a high-angle linear array, trending away from the MORE field on Pb-isotopic covariation diagrams; have the highest Sr- and lowest Nd-isotopic compositions, of the two chains (but nevertheless plotting above bulk earth on the 87Sr/86Sr versus 143Nd/144Nd covariation diagram); and exhibit Sm/Nd and Rb/Sr values that are lower and higher, respectively, than the estimated values for bulk earth. While the Sm/Nd and Rb/Sr characteristics are common to both chains, volcanoes associated with the Philippine-East Luzon trench have Pb-isotopic compositions that fall in the Indian Ocean MORB field and that require time-integrated evolution in a high Th/U environment. They also have higher Nd- and lower Sr-isotopic ratios. The source materials of Philippine volcanoes, therefore, have undergone varied recent enrichments in LILE, as indicated by the decoupling of isotopic and elemental ratios. These enrichments, particularly for the western volcanoes, cannot be entirely due to small degrees of partial melting in the mantle wedge, considering that they were accompanied by elevations in radiogenic Pb. Elevated Pb ratios are best explained by the introduction of subducted, continentally derived sediments. The sedimentary component in the western volcanoes is probably the South China Sea sediments derived largely from Eurasia. That this component is not available in the Philippine-East Luzon trench is reflected by the fact that the eastern volcanoes

  6. Determination of 90Sr and Pu isotopes in contaminated groundwater samples by inductively coupled plasma mass spectrometry

    NASA Astrophysics Data System (ADS)

    Zoriy, Miroslav V.; Ostapczuk, Peter; Halicz, Ludwik; Hille, Ralf; Becker, J. Sabine

    2005-04-01

    A sensitive analytical method for determining the artificial radionuclides 90Sr, 239Pu and 240Pu at the ultratrace level in groundwater samples from the Semipalatinsk Test Site area in Kazakhstan by double-focusing sector field inductively coupled plasma mass spectrometry (ICP-SFMS) was developed. In order to avoid possible isobaric interferences at m/z 90 for 90Sr determination (e.g. 90Zr+, 40Ar50Cr+, 36Ar54Fe+, 58Ni16O2+, 180Hf2+, etc.), the measurements were performed at medium mass resolution under cold plasma conditions. Pu was separated from uranium by means of extraction chromatography using Eichrom TEVA resin with a recovery of 83%. The limits of detection for 90Sr, 239Pu and 240Pu in water samples were determined as 11, 0.12 and 0.1 fg ml-1, respectively. Concentrations of 90Sr and 239Pu in contaminated groundwater samples ranged from 18 to 32 and from 28 to 856 fg ml-1, respectively. The 240Pu/239Pu isotopic ratio in groundwater samples was measured as 0.17. This isotope ratio indicates that the most probable source of contamination of the investigated groundwater samples was the nuclear weapons tests at the Semipalatinsk Test Site conducted by the USSR in the 1960s.

  7. Bayesian Integration of Isotope Ratio for Geographic Sourcing of Castor Beans

    DOE PAGES

    Webb-Robertson, Bobbie-Jo; Kreuzer, Helen; Hart, Garret; ...

    2012-01-01

    Recenmore » t years have seen an increase in the forensic interest associated with the poison ricin, which is extracted from the seeds of the Ricinus communis plant. Both light element (C, N, O, and H) and strontium (Sr) isotope ratios have previously been used to associate organic material with geographic regions of origin. We present a Bayesian integration methodology that can more accurately predict the region of origin for a castor bean than individual models developed independently for light element stable isotopes or Sr isotope ratios. Our results demonstrate a clear improvement in the ability to correctly classify regions based on the integrated model with a class accuracy of 60.9 ± 2.1 % versus 55.9 ± 2.1 % and 40.2 ± 1.8 % for the light element and strontium (Sr) isotope ratios, respectively. In addition, we show graphically the strengths and weaknesses of each dataset in respect to class prediction and how the integration of these datasets strengthens the overall model.« less

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

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Webb-Robertson, Bobbie-Jo M.; Kreuzer, Helen W.; Hart, Garret L.

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

  9. Bayesian Integration of Isotope Ratio for Geographic Sourcing of Castor Beans

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Webb-Robertson, Bobbie-Jo; Kreuzer, Helen; Hart, Garret

    Recenmore » t years have seen an increase in the forensic interest associated with the poison ricin, which is extracted from the seeds of the Ricinus communis plant. Both light element (C, N, O, and H) and strontium (Sr) isotope ratios have previously been used to associate organic material with geographic regions of origin. We present a Bayesian integration methodology that can more accurately predict the region of origin for a castor bean than individual models developed independently for light element stable isotopes or Sr isotope ratios. Our results demonstrate a clear improvement in the ability to correctly classify regions based on the integrated model with a class accuracy of 60.9 ± 2.1 % versus 55.9 ± 2.1 % and 40.2 ± 1.8 % for the light element and strontium (Sr) isotope ratios, respectively. In addition, we show graphically the strengths and weaknesses of each dataset in respect to class prediction and how the integration of these datasets strengthens the overall model.« less

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

    USGS Publications Warehouse

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

    2013-01-01

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

  11. A method for combined Sr-Nd-Hf isotopic analysis of <10 mg dust samples: implication for ice core science

    NASA Astrophysics Data System (ADS)

    Ujvari, Gabor; Wegner, Wencke; Klötzli, Urs

    2017-04-01

    Aeolian mineral dust particles below the size of 10-20 μm often experience longer distance transport in the atmosphere, and thus Aeolian dust is considered an important tracer of large-scale atmospheric circulation. Since ice core dust is purely Aeolian in origin, discrimination of its potential source region(s) can contribute to a better understanding of past dust activity and climatic/environmental causes. Furthermore, ice core dust source information provides critical experimental constraints for model simulations of past atmospheric circulation patterns [1,2]. However, to identify dust sources in past dust archives such as ice cores, the mineralogy and geochemistry of the wind-blown dust material must be characterized. While the amount of dust in marine cores or common terrestrial archives is sufficient for different types of analyses and even for multiple repeat measurements, dust content in ice cores is usually extremely low even for the peak dusty periods such as the Last Glacial Maximum (LGM) (5-8 mg dust/kg ice; [3]). Since the most powerful dust fingerprinting methods, such as REE composition and Sr-Nd-Pb isotopic analyses are destructive there is a clear need to establish sequential separation techniques of Sr, Nd, Pb and other REEs to get the most information out of small (5-10 mg) dust samples recovered from ice cores. Although Hf isotopes have recently been added as a robust tool of aerosol/dust source discrimination (e.g. [4,5,6,7]), precise Hf isotopic measurements of small (<10 mg) dust samples are still challenging due to the small Hf amounts (on the order of 1-10 ng) and often compromised by potential problems arising during ion exchange chemistry. In this pilot study an improved method for chemical separation of Sr, Nd and Hf by Bast et al. [8] was applied, which allows the precise isotope analysis of sub-ng amounts of Hf by MC-ICPMS. This ion exchange chromatography procedure has been combined with established methods of separating and

  12. Evolution of the upper mantle beneath the southern Baikal rift zone: an Sr-Nd isotope study of xenoliths from the Bartoy volcanoes

    NASA Astrophysics Data System (ADS)

    Ionov, D. A.; Kramm, U.; Stosch, H.-G.

    1992-06-01

    Anhydrous and amphibole-bearing peridotite xenoliths occur in roughly equal quantitites in the Bartoy volcanic field about 100 km south of the southern tip of Lake Baikal in Siberia (Russia). Whole-rock samples and pure mineral separates from nine xenoliths have been analyzed for Sr and Nd isotopes in order to characterize the upper mantle beneath the southern Baikal rift zone. In an Sr-Nd isotope diagram both dry and hydrous xenoliths from Bartoy plot at the junction between the fields of MORB and ocean island basalts. This contrasts with data available on two other localities around Lake Baikal (Tariat and Vitim) where peridotites typically have Sr-Nd isotope compositions indicative of strong long-term depletion in incompatible elements. Our data indicate significant chemical and isotopic heterogeneity in the mantle beneath Bartoy that may be attributed to its position close to an ancient suture zone separating the Siberian Platform from the Mongol-Okhotsk mobile belt and occupied now by the Baikal rift. Two peridotites have clinopyroxenes depleted in light rare earth elements (LREE) with Sr and Nd model ages of about 2 Ga and seem to retain the trace element and isotopic signatures of old depleted lithospheric mantle, while all other xenoliths show different degrees of LREE-enrichment. Amphiboles and clinopyroxenes in the hydrous peridotites are in Sr-Nd isotopic disequilibrium. If this reflects in situ decay of 147Sm and 87Rb rather than heterogeneities produced by recent metasomatic formation of amphiboles then 300 400 Ma have passed since the minerals were last in equilibrium. This age range then indicates an old enrichment episode or repeated events during the Paleozoic in the lithospheric mantle initially depleted maybe ˜2 Ga ago. The Bartoy hydrous and enriched dry peridotites, therefore, are unlikely to represent fragments of a young asthenospheric bulge which, according to seismic reflection studies, reached the Moho at the axis of the Baikal rift zone

  13. Veined pyroxenite xenoliths in Ugandan kamafugites: mantle or magma? Using in situ techniques for 87Sr/86Sr-isotopes and trace elements as tools

    NASA Astrophysics Data System (ADS)

    Link, Klemens; Tommasini, Simone; Braschi, Eleonora; Conticelli, Sandro; Barifaijo, Erasmus; Tiberindwa, John V.; Foley, Stephen F.

    2010-05-01

    The genesis of pyroxenite nodules in Ugandan kamafugites and their possible genetic relationships is a matter of debate. In earlier studies the pyroxenites were considered either as xenoliths from pervasively metasomatized peridotite mantle (Lloyd, 1981) or as distinct paragenesises occurring as veins within the peridotitic mantle (Harte et al., 1993). In both cases the xenoliths would represent mantle material that was at least partly involved as source material for the kamafugite melts. A third alternative could be that they represent cumulates of the lavas. In any case, the nodules provide important information for understanding the generation of ultrapotassic lavas and for characterizing the rift-related lithosphere mantle as part of the initial continental rift process. Originally the ultrapotassic kamafugites were considered to be single stage partial melts of pervasively metasomatized mantle but new geochemical studies indicate a multistage development (Rosenthal et al., 2009). Nd, Hf and Os isotopes point to mixing between components derived from metasomatically influenced peridotite and mica-pyroxenite. In-situ investigation of the Sr-isotope and trace element compositions of individual minerals in a number of xenoliths allows us to constrain their genesis and relation to the host lavas. The nodules appear to originate by near-liquidus crystallization of melts derived from enriched peridotite within the cratonic lithosphere mantle. They later partially remelted to form one source of the potassium-rich kamafugites. Sr-isotopes from different domains within single mineral grains in the nodules and host lavas are used to trace the nodules' role as a potential source to lavas, and trace element measurements are used to support the conclusions. Rb/Sr- measurements from the biotites to constrain the time between nodule crystallization and eruption of the Quaternary lavas to about 3.3 Ma. This also suggests a significant increase of the geothermal gradient

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

    USGS Publications Warehouse

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

    1983-01-01

    Isotopic ratios and trace element abundances were measured on samples of Ir-enriched clay at the Cretaceous-Tertiary boundary, and in carbonate and marl from 5 cm below and 3 cm above the boundary. Samples were leached with acetic acid to remove carbonate, and with hydrochloric acid. Leachates and residues were measured. The Sr, Nd, O and H isotopic compositions of the boundary clay residues are distinct from those of the stratigraphically neighboring materials. The data indicate that most of the clay material was derived from a terrestrial source with relatively low 87Sr/86Sr and high 143Nd/144Nd ratios. The ??18O data suggest that the detritus has been modified by submarine weathering. K-Ca and Rb-Sr systematics, as well as O isotope ratios of K-feldspar spherules within the boundary clay, suggest that they are predominantly authigenic and may have formed after the time of deposition. However, Sm-Nd and Rb-Sr isotopic data indicate that the spherules contain relict material that provides information on the nature of the original detritus. The isotopic evidence for foreign terrestrial detritus in the boundary clay, the low rare earth element concentrations and high Ni concentration, support the hypothesis of a terminal Cretaceous asteroidal impact that produced a global layer of fallout. The data are most easily explained if the impact site was on oceanic crust rather than continental crust, and if a substantial fraction of the fallout was derived from relatively deep within the lithosphere (>3 km). This would probably require a single large impactor. ?? 1983.

  15. Tracing mineral weathering reactions in the critical zone using Mg, Ca, and Sr isotopes, Luquillo Mountains, Puerto Rico

    NASA Astrophysics Data System (ADS)

    Buss, H. L.; White, A. F.; Vivit, D.; Bullen, T. D.; Blum, A. E.; Dessert, C.; Gaillardet, J.

    2008-12-01

    Mineral weathering in the critical zone directly impacts the availability of many important soil nutrients. As part of the USGS Water Energy and Biogeochemical Budgets (WEBB) program and the Critical Zone Exploration Network, we are investigating mineral nutrient distributions and fluxes in depth profiles (to 16 m) at five sites in the Bisley 1 catchment in the Luquillo Mountains of Puerto Rico. The Bisley 1 catchment contains a thick regolith developed on marine bedded, andesitic, volcaniclastic bedrock. Pore waters were sampled as a function of depth from nested suction water samplers. Pore water chemistry was analyzed and compared to total chemistry of solid samples taken from augered cores. Mg, Ca and Sr isotope ratios were measured of the pore waters at the Institut de Physique du Globe de Paris (Mg) and at the USGS in Menlo Park, CA (Ca, Sr). The Mg isotope ratios increase with increasing depth from δ26Mg = -0.772 at the surface to - 0.267 at depth, relative to the DSM3 standard. Sr isotope ratios vary from 0.70922 to 0.71016 87Sr/86Sr, with no discernible depth trend. The regolith is highly weathered and is depleted in primary minerals (except quartz) with respect to bedrock. Volumetric strain, calculated with respect to quartz, indicates approximately 25% volume collapse occurred relative to the original volume of the bedrock. Plagioclase, chlorite, pyroxene, and amphibole weather at the bedrock-regolith interface. The regolith contains quartz, kaolinite, other clays, and iron and manganese oxides. Increasing solid and pore water Mg concentrations and δ26Mg with depth likely indicate a two step weathering process wherein high-Mg chlorite dissolves at the bedrock-regolith interface and forms Mg-containing secondary clays and oxides, which then dissolve within the regolith profile.

  16. Tracing of aerosol sources in an urban environment using chemical, Sr isotope, and mineralogical characterization.

    PubMed

    Duarte, Regina M B O; Matos, João T V; Paula, Andreia S; Lopes, Sónia P; Ribeiro, Sara; Santos, José Francisco; Patinha, Carla; da Silva, Eduardo Ferreira; Soares, Rosário; Duarte, Armando C

    2017-04-01

    In the framework of two national research projects (ORGANOSOL and CN-linkAIR), fine particulate matter (PM 2.5 ) was sampled for 17 months at an urban location in the Western European Coast. The PM 2.5 samples were analyzed for organic carbon (OC), water-soluble organic carbon (WSOC), elemental carbon (EC), major water-soluble inorganic ions, mineralogical, and for the first time in this region, strontium isotope ( 87 Sr/ 86 Sr) composition. Organic matter dominates the identifiable urban PM 2.5 mass, followed by secondary inorganic aerosols. The acquired data resulted also in a seasonal overview of the carbonaceous and inorganic aerosol composition, with an important contribution from primary biomass burning and secondary formation processes in colder and warmer periods, respectively. The fossil-related primary EC seems to be continually present throughout the sampling period. The 87 Sr/ 86 Sr ratios were measured on both the labile and residual PM 2.5 fractions as well as on the bulk PM 2.5 samples. Regardless of the air mass origin, the residual fractions are more radiogenic (representative of a natural crustal dust source) than the labile fractions, whose 87 Sr/ 86 Sr ratios are comparable to that of seawater. The 87 Sr/ 86 Sr ratios and the mineralogical composition data further suggest that sea salt and mineral dust are important primary natural sources of fine aerosols throughout the sampling period.

  17. Effects of interaction between ultramafic tectonite and mafic magma on Nd-Pb-Sr isotopic systems in the Neoproterozoic Chaya Massif, Baikal-Muya ophiolite belt

    NASA Astrophysics Data System (ADS)

    Amelin, Yuri V.; Ritsk, Eugeni Yu.; Neymark, Leonid A.

    1997-04-01

    Sm-Nd, Rb-Sr and U-Pb isotopic systems have been studied in minerals and whole rocks of harzburgites and mafic cumulates from the Chaya Massif, Baikal-Muya ophiolite belt, eastern Siberia, in order to determine the relationship between mantle ultramafic and crustal mafic sections. Geological relations in the Chaya Massif indicate that the mafic magmas were emplaced into, and interacted with older solid peridotite. Hand picked, acid-leached, primary rock-forming and accessory minerals (olivine, orthopyroxene, clinopyroxene and plagioclase) from the two harzburgite samples show coherent behavior and yield 147Sm/ 144Nd- 143Nd/ 144Nd and 238U/ 204Pb- 206Pb/ 204Pb mineral isochrons, corresponding to ages of 640 ± 58 Ma (95% confidence level) and 620 ± 71 Ma, respectively. These values are indistinguishable from the crystallization age of the Chaya mafic units of 627 ± 25 Ma (a weighted average of internal isochron Sm-Nd ages of four mafic cumulates). The Rb-Sr and Sm-Nd isotopic systems in the harzburgite whole-rock samples were disturbed by hydrothermal alteration. These alteration-related isotopic shifts mimic the trend of variations in primary isotopic compositions in the mafic sequence, thus emphasizing that isotopic data for ultramafic rocks should be interpreted with great caution. On the basis of initial Sr and Nd values, ultramafic and mafic rocks of the Chaya Massif can be divided into two groups: (1) harzburgites and the lower mafic unit gabbronorites withɛ Nd = +6.6 to +7.1 andɛ Sr = -11 to -16; and (2) websterite of the lower unit and gabbronorites of the upper mafic unit:ɛ Nd = +4.6 to +6.1 andɛ Sr = -8 to -9. Initial Pb isotopic ratios are identical in all rocks studied, with mean values of 206Pb/ 204Pb= 16.994 ± 0.023 and 207Pb/ 204Pb= 15.363 ± 0.015. The similarity of ages and initial isotopic ratios within the first group indicates that the isotopic systems in the pre-existing depleted peridotite were reset by extensive interaction with

  18. Effects of interaction between ultramafic tectonite and mafic magma on Nd-Pb-Sr isotopic systems in the Neoproterozoic Chaya Massif, Baikal-Muya ophiolite belt

    USGS Publications Warehouse

    Amelin, Y.V.; Ritsk, E. Yu; Neymark, L.A.

    1997-01-01

    Sm-Nd, Rb-Sr and U-Pb isotopic systems have been studied in minerals and whole rocks of harzburgites and mafic cumulates from the Chaya Massif, Baikal-Muya ophiolite belt, eastern Siberia, in order to determine the relationship between mantle ultramafic and crustal mafic sections. Geological relations in the Chaya Massif indicate that the mafic magmas were emplaced into, and interacted with older solid peridotite. Hand picked, acid-leached, primary rock-forming and accessory minerals (olivine, orthopyroxene, clinopyroxene and plagioclase) from the two harzburgite samples show coherent behavior and yield 147Sm/144Nd- 143Nd/144Nd and 238U/204Pb-206Pb/204Pb mineral isochrons, corresponding to ages of 640 ?? 58 Ma (95% confidence level) and 620 ?? 71 Ma, respectively. These values are indistinguishable from the crystallization age of the Chaya mafic units of 627 ?? 25 Ma (a weighted average of internal isochron Sm-Nd ages of four mafic cumulates). The Rb-Sr and Sm-Nd isotopic systems in the harzburgite whole-rock samples were disturbed by hydrothermal alteration. These alteration-related isotopic shifts mimic the trend of variations in primary isotopic compositions in the mafic sequence, thus emphasizing that isotopic data for ultramafic rocks should be interpreted with great caution. On the basis of initial Sr and Nd values, ultramafic and mafic rocks of the Chaya Massif can be divided into two groups: (1) harzburgites and the lower mafic unit gabbronorites with ??Nd = +6.6 to +7.1 and ??Sr = -11 to -16; and (2) websterite of the lower unit and gabbronorites of the upper mafic unit: ??Nd = + 4.6 to + 6.1 and ??Sr = - 8 to -9. Initial Pb isotopic ratios are identical in all rocks studied, with mean values of 206Pb/204Pb = 16.994 ?? 0.023 and 207Pb/204Pb = 15.363 ?? 0.015. The similarity of ages and initial isotopic ratios within the first group indicates that the isotopic systems in the pre-existing depleted peridotite were reset by extensive interaction with basaltic

  19. Major, trace element and isotope geochemistry (Sr-Nd-Pb) of interplinian magmas from Mt. Somma-Vesuvius (Southern Italy)

    USGS Publications Warehouse

    Somma, R.; Ayuso, R.A.; de Vivo, B.; Rolandi, G.

    2001-01-01

    Major, trace element and isotopic (Sr, Nd, Pb) data are reported for representative samples of interplinian (Protohistoric, Ancient Historic and Medieval Formations) activity of Mt. Somma-Vesuvius volcano during the last 3500 years. Tephra and lavas exhibit significant major, trace element and isotopic variations. Integration of these data with those obtained by previous studies on the older Somma suites and on the latest activity, allows to better trace a complete petrological and geochemical evolution of the Mt. Somma-Vesuvius magmatism. Three main groups of rocks are recognized. A first group is older than 12.000 yrs, and includes effusive-explosive activity of Mt. Somma. The second group (8000-2700 yrs B.P.) includes the products emitted by the Ottaviano (8000 yrs. B.P.) and Avellino (3550 yrs B.P.) plinian eruptions and the interplinian activity associated with the Protohistoric Formation. Ancient Historic Formation (79-472 A.D.), Medieval Formation (472-1139 A.D.) and Recent interplinian activity (1631-1944 A.D.) belong to the third group of activity (79-1944 A.D.). The three groups of rocks display distinct positive trends of alkalis vs. silica, which become increasingly steeper with age. In the first group there is an increase in silica and alkalis with time, whereas an opposite tendency is observed in the two younger groups. Systematic variations are also evident among the incompatible (Pb, Zr, Hf, Ta, Th, U, Nb, Rb, Cs, Ba) and compatible elements (Sr, Co, Cr). REE document variable degrees of fractionation, with recent activity displaying higher La/Yb ratios than Medieval and Ancient Historic products with the same degree of evolution. N-MORB normalized multi-element diagrams for interplinian rocks show enrichment in Rb, Th, Nb, Zr and Sm (> *10 N-MORB). Sr isotope ratios are variable, with Protohistoric rocks displaying 87Sr/86Sr= 0.70711-0.70810, Ancient Historic 87Sr/86Sr=0.70665-0.70729, and Medieval 87Sr/86Sr=0.70685-0.70803. Neodymium isotopic

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

    NASA Technical Reports Server (NTRS)

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

    2012-01-01

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

  1. A Coast Mountains provenance for the Valdez and Orca groups, southern Alaska, based on Nd, Sr, and Pb isotopic evidence

    USGS Publications Warehouse

    Farmer, G.L.; Ayuso, R.; Plafker, G.

    1993-01-01

    Nd, Sr, and Pb isotopic data were obtained for fourteen fine- to coarse-grained samples of accreted flysch of the Late Cretaceous and early Tertiary Valdez and Orca Groups in southern Alaska to determine the flysch provenance. Argillites and greywackes from the Orca Group, as well as compositionally similar but higher metamorphic grade rocks from the Valdez Group, show a restricted range of correlated ??{lunate}Nd ( -0.6 to -3.8) and 87Sr 86Sr (0.7060-0.7080) at the time of sediment deposition ( ??? 50 Ma). Pb isotopic compositions also vary over a narrow range ( 206Pb 204Pb = 19.138-19.395, 207Pb 204Pb = 15.593-15.703, 208Pb 204Pb = 38.677-39.209), and in the Orca Group the samples generally become more radiogenic with decreasing ??{lunate}Nd and increasing 87Sr 86Sr. All samples have similar trace element compositions characterized by moderate light rare earth element enrichments, and low ratios of high field strength elements to large ion lithophile elements. Based on petrographic, geochemical, and isotopic data the sedimentary rocks are interpreted to have been derived largely from a Phanerozoic continental margin arc complex characterized by igneous rocks with ??{lunate}Nd values between 0 and -5. The latter conclusion is supported by the ??{lunate}Nd values of a tonalite clast and a rhyodacite clast in the Orca Group (??{lunate}Nd = -4.9 and -0.9, respectively). However, trondjemitic clasts in the Orca Group have significantly lower ??{lunate}Nd ( ??? -10) and require a derivation of a portion of the flysch from Precambrian crustal sources. The Nd, Sr, and Pb isotopic compositions of both the Valdez and Orca Groups overlap the values determined for intrusive igneous rocks exposed within the northern portion of the Late Cretaceous to early Tertiary Coast Mountains Plutonic Complex in western British Columbia and equivalent rocks in southeastern Alaska. The isotopic data support previous conclusions based on geologic studies which suggest that the flysch was

  2. Geochemical structure of the Hawaiian plume: Sr, Nd, and Os isotopes in the 2.8 km HSDP-2 section of Mauna Kea volcano

    NASA Astrophysics Data System (ADS)

    Bryce, Julia G.; Depaolo, Donald J.; Lassiter, John C.

    2005-09-01

    Sr, Nd, and Os isotopic measurements were made on 110 Mauna Kea lava and hyaloclastite samples from the drillcore retrieved from the second phase of the Hawaii Scientific Drilling Project (HSDP-2). The samples come from depths of 255 to 3098 meters below sea level, span an age range from 200 to about 550-600 kyr, and represent an ordered record of the lava output from Mauna Kea volcano as it drifted a distance of about 40 km over the magma-producing region of the Hawaiian hot spot. The deepest (oldest) samples represent the time when Mauna Kea was closest to the center of the melting region of the Hawaiian plume. The Sr and Os isotopic ratios in HSDP-2 lavas show only subtle isotopic shifts over the ˜400 kyr history represented by the core. Neodymium isotopes (ɛNd values) increase systematically with decreasing age from an average value of nearly +6.5 to an average value of +7.5. This small change corresponds to subtle shifts in 87Sr/86Sr and 187Os/188Os isotope ratios, with small shifts of ɛHf, a large shift in 208Pb/204Pb and 208Pb/207Pb values, and with a very large shift in He isotope ratios from R/RA values of about 7-8 to values as high as 25. When Mauna Kea was closest to the plume core, the magma source did not have primitive characteristics for Nd, Sr, Pb, Hf, and Os isotopes but did have variable amounts of "primitive" helium. The systematic shifts in Nd, Hf, Pb, and He isotopes are consistent with radial isotopic zoning within the melting region of the plume. The melting region constitutes only the innermost, highest-temperature part of the thermally anomalous plume mantle. The different ranges of values observed for each isotopic system, and comparison of Mauna Kea lavas with those of Mauna Loa, suggest that the axial region of the plume, which has a radius of ˜20 km, is a mixture of recycled subducted components and primitive lower mantle materials, recently combined during the formational stages of the plume at the base of the mantle. The

  3. Sr and Mg Isotopes of post-glacial limestones: implications for the chemical evolution of the Neoproterozoic Ocean after snowball earth

    NASA Astrophysics Data System (ADS)

    Liu, C.; Wang, Z.; Macdonald, F. A.

    2013-12-01

    The variation of ocean chemistry after the Marinoan (~635Ma) glaciation reflects the integrated effect of changes in continental weathering, carbonate precipitation and hydrothermal process in response to the extreme climatic event. To reconstruct the contemporary seawater chemistry, we analyzed Sr and Mg isotopes of the post-glacial carbonate overlying cap dolostones in the basal Ediacaran Ol Formation of the Tsagaan Olom Group in southwestern Mongolia. We employed an incremental leaching technique by dissolving carbonates sequentially with ammonium acetate and increasing concentrations of acetic acid to separate metals from various mineral phases in the carbonate (including surface adsorbed phases, calcite and dolomite). The leachates from each step and the dissolved bulk samples passed through chromatographic columns to extract pure Mg and Sr, which were then analyzed for their isotopic compositions by MC-ICP-MS (Neptune) at Yale University. Elemental ratios (Mg/Ca and Sr/(Mg+Ca)) in each leaching steps were measured as well. The following observations were noted from these experiments. First, the Mg/Ca ratio of the leachate decreased in the first few steps, reached a plateau in the middle steps and increased in the last few steps, implying a leaching sequence of surface-adsorbed phases, calcite and dolomite. Second, the Sr/(Mg+Ca) ratios remain almost constant except in the first two steps, suggesting similar Sr concentrations in different carbonates but elevated values in surface-adsorbed phases. Third, variations of both δ26MgDSM3 and 87Sr/86Sr values of the leachates with leaching steps exhibit similar trends to Mg/Ca, indicating enrichment of 26Mg and 87Sr in dolomite. Fourth, 87Sr/86Sr values of the leachates exhibit a wider plateau than δ26MgDSM3, denoting a binary mixing of dissolved calcite and dolomite in the last few steps. Finally, higher 87Sr/86Sr ratios and δ26MgDSM3 values were observed for bulk samples than their calcite components. The 87Sr

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

    EPA Science Inventory

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

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

    NASA Astrophysics Data System (ADS)

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

    2014-03-01

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

  6. Recoil distance method lifetime measurement of the 21+ state in 94Sr and implications for the structure of neutron-rich Sr isotopes

    NASA Astrophysics Data System (ADS)

    Chester, A.; Ball, G. C.; Caballero-Folch, R.; Cross, D. S.; Cruz, S.; Domingo, T.; Drake, T. E.; Garnsworthy, A. B.; Hackman, G.; Hallam, S.; Henderson, J.; Henderson, R.; Korten, W.; Krücken, R.; Moukaddam, M.; Olaizola, B.; Ruotsalainen, P.; Smallcombe, J.; Starosta, K.; Svensson, C. E.; Williams, J.; Wimmer, K.

    2017-07-01

    A high precision lifetime measurement of the 21+ state in 94Sr was performed at TRIUMF's ISAC-II facility by coupling the recoil distance method implemented via the TIGRESS integrated plunger with unsafe Coulomb excitation in inverse kinematics. Due to limited statistics imposed by the use of a radioactive 94Sr beam, a likelihood ratio χ2 method was derived and used to compare experimental data to Geant4 simulations. The B (E 2 ;21+→01+) value extracted from the lifetime measurement of 7 .80-0.40+0.50(stat.)±0.07 (sys.) ps is approximately 25% larger than previously reported while the relative error has been reduced by a factor of approximately 8. A baseline deformation has been established for Sr isotopes with N ≤58 which is a necessary condition for the quantum phase transition interpretation of the onset of deformation in this region. A comparison to existing theoretical models is presented.

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

    NASA Technical Reports Server (NTRS)

    Depaolo, D. J.; Kyte, F. T.; Marshall, B. D.; Oneil, J. R.; Smit, J.

    1983-01-01

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

  8. Thermal evolution of Site U1414 by stable isotopes δ13C and δ18O, 87Sr/86Sr and fluid inclusion analyses, IODP Expedition 344

    NASA Astrophysics Data System (ADS)

    Brandstätter, Jennifer; Kurz, Walter; Krenn, Kurt; Richoz, Sylvain

    2017-04-01

    IODP Expedition 344 is the second expedition in course of the Costa Rica Seismogenesis Project (Program A), that was designed to reveal processes that effect nucleation and seismic rupture of large earthquakes at erosional subduction zones. Site 344-U1414, located 1 km seaward of the deformation front offshore Costa Rica, serves to evaluate fluid-rock interaction and geochemical processes linked with the tectonic evolution of the incoming Cocos Plate from the Early Miocene up to recent times. Combined isotope analyses and microthermometric analyses of fluid inclusions of hydrothermal veins within lithified sediments and the igneous basement (Cocos Ridge basalt), was used to reveal the thermal history of Site 344-U1414. Veins in the sedimentary rocks are mainly filled by coarse-grained calcite and subordinately by quartz. Veins within the basalt show polymineralic filling of clay minerals, calcite, aragonite and quartz. Blocky veins with embedded wall rock fragments, appearing in the sediments and in the basalt, indicate hydraulic fracturing. The carbon isotopic composition of the vein calcite suggest the influence of a CO2 -rich fluid mixed with seawater (-3.0 to -0.4‰ V-PDB) and the δ18O values can be differentiated in two groups, depending on the formation temperature (-13.6 to -9.3‰ and -10.8 to -4.7‰ V-PDB). 87Sr/86Sr ratios from the veins confirm the results of the stable isotope analyses, with a higher 87Sr/86Sr ratio close to seawater composition and lower ratios indicating the influence of basalt alteration. The hydrothermal veins contain different types of fluid inclusions with high and low entrapment temperatures and low saline fluids. The occurrence of decrepitated fluid inclusions, formed by increased internal overpressure, is related to isobaric heating. Elongated fluid inclusion planes, arc-like fluid inclusions and low homogenization temperatures suggest subsequent isobaric cooling. The stable isotopic content, strontium isotopic composition

  9. Laser cooling and imaging of individual radioactive +90Sr ions

    NASA Astrophysics Data System (ADS)

    Jung, Kyunghun; Iwata, Yoshihiro; Miyabe, Masabumi; Yamamoto, Kazuhiro; Yonezu, Tomohisa; Wakaida, Ikuo; Hasegawa, Shuichi

    2017-10-01

    We have developed an apparatus integrating resonance-ionization, ion-trap, and laser-cooling techniques for an ultratrace radioactive isotope 90Sr analysis. Trapped +90Sr isotope ions were laser cooled, and their 4 d 3/2 2D →5 p 1/2 2P transition isotope shift was experimentally measured to be -281 (17 ) MHz by comparing individual spectra of +88Sr and +90Sr ions. Crystallization of +90Sr was carried out using the resonance frequency value confirmed in our experiment, and then +90Sr individual ions were successfully observed.

  10. Petrogenesis and origin of the Upper Jurassic-Lower Cretaceous magmatism in Central High Atlas (Morocco): Major, trace element and isotopic (Sr-Nd) constraints

    NASA Astrophysics Data System (ADS)

    Essaifi, Abderrahim; Zayane, Rachid

    2018-01-01

    During an uplift phase, which lasted ca. 40 Ma, from the Late Jurassic (165 Ma) to the Early Cretaceous (125 Ma), transitional to moderately alkaline magmatic series were emplaced in the Central High Atlas. The corresponding magmatic products include basaltic lava flows erupted within wide synclines and intrusive complexes composed of layered mafic intrusions and monzonitic to syenitic dykes emplaced along narrow anticlinal ridges. The igneous rock sequence within the intrusive complexes is composed of troctolites, olivine-gabbros, oxide-gabbros, monzonites and syenites. The chemical compositions of the various intrusive rocks can be accounted for by crystal accumulation, fractional crystallization and post-magmatic remobilization. The evolution from the troctolites to the syenites was mainly controlled by a fractional crystallization process marked by early fractionation of olivine, plagioclase and clinopyroxene, followed by separation of biotite, amphibole, apatite, and Ti-magnetite. Hydrothermal activity associated with emplacement of the intrusions within the Jurassic limestones modified the elemental and the Sr isotopic composition of the hydrothermally altered rocks In particular the monzonitic to syenitic dykes underwent an alkali metasomatism marked by depletion in K and Rb and enrichment in Na and Sr. As a result, their Sr isotopic composition was shifted towards higher initial Sr isotopic ratios (0.7067-0.7075) with respect to the associated gabbros (0.7036-0.7046). On the contrary, the Nd isotopic compositions were preserved from isotope exchange with the limestones and vary in a similar range to those of the gabbros (+1.6 < εNdi < +4.1). The isotopic and the trace element ratios of the uncontaminated samples were used to constrain the source characteristics of this magmatism. The Sr-Nd isotopic data and the incompatible element ratios (e.g. La/Nb, Zr/Nb, Th/U, Ce/Pb) are consistent with generation from an enriched upper mantle similar to an ocean

  11. Isotopic imprints of mountaintop mining contaminants.

    PubMed

    Vengosh, Avner; Lindberg, T Ty; Merola, Brittany R; Ruhl, Laura; Warner, Nathaniel R; White, Alissa; Dwyer, Gary S; Di Giulio, Richard T

    2013-09-03

    Mountaintop mining (MTM) is the primary procedure for surface coal exploration within the central Appalachian region of the eastern United States, and it is known to contaminate streams in local watersheds. In this study, we measured the chemical and isotopic compositions of water samples from MTM-impacted tributaries and streams in the Mud River watershed in West Virginia. We systematically document the isotopic compositions of three major constituents: sulfur isotopes in sulfate (δ(34)SSO4), carbon isotopes in dissolved inorganic carbon (δ(13)CDIC), and strontium isotopes ((87)Sr/(86)Sr). The data show that δ(34)SSO4, δ(13)CDIC, Sr/Ca, and (87)Sr/(86)Sr measured in saline- and selenium-rich MTM impacted tributaries are distinguishable from those of the surface water upstream of mining impacts. These tracers can therefore be used to delineate and quantify the impact of MTM in watersheds. High Sr/Ca and low (87)Sr/(86)Sr characterize tributaries that originated from active MTM areas, while tributaries from reclaimed MTM areas had low Sr/Ca and high (87)Sr/(86)Sr. Leaching experiments of rocks from the watershed show that pyrite oxidation and carbonate dissolution control the solute chemistry with distinct (87)Sr/(86)Sr ratios characterizing different rock sources. We propose that MTM operations that access the deeper Kanawha Formation generate residual mined rocks in valley fills from which effluents with distinctive (87)Sr/(86)Sr and Sr/Ca imprints affect the quality of the Appalachian watersheds.

  12. Is the Modern Marine 87Sr/86Sr Cycle Balanced?

    NASA Astrophysics Data System (ADS)

    Peucker-Ehrenbrink, B.

    2017-12-01

    The marine 87Sr/86Sr record is one of the best-reconstructed isotope records with thousands of high quality measurements spanning the past 800 million years. It records a global signal of tectonic, biotic and climatic processes on Earth. Yet despite decades of research we still do not know whether the current marine Sr budget is in steady state. Studies of the marine 88Sr/86Sr record indicate that sources and sinks do not balance. The magnitude and isotope composition of the terrestrial inputs are being debated, and the magnitude and temporal variability of unradiogenic contributions are not well constrained. Here I provide a revised assessment of all continental sources of Sr to the ocean, including river runoff, submarine groundwater discharge (Beck et al., 2013), dissolution of riverine suspended matter in seawater and dissolution of volcanic ash deposited on the ocean (Jones et al., 2012). I contrast continental sources of Sr with estimates of marine sources of Sr to seawater, specifically high- and low-temperature submarine hydrothermal fluids, as well as diffusive diagenetic fluxes. Best current data imply that unradiogenic submarine hydrothermal inputs to seawater are insufficient to balance the flux of radiogenic continental Sr. The revised assessment of riverine contributions is based on Sr data for almost 230 rivers, an increasing amount of time-series data for such rivers, as well as river discharge and sediment flux data for more than 2000 rivers. Regional sampling biases have been corrected with the aid of digital bedrock maps, specifically along the western margin of North America, East Africa and the large drainage region of Arabia, India and SE Asia. Significant uncertainty in the chemical and isotopic compositions of runoff from Greenland and East Africa remains. The main uncertainty in the budget, however, is related to the possibility that modern rivers do not represent the pre-anthropogenic (natural) state of continental runoff (e.g. Ganges

  13. Insights into the diagenetic environment of fossil marine vertebrates of the Pisco Formation (late Miocene, Peru) from mineralogical and Sr-isotope data

    NASA Astrophysics Data System (ADS)

    Gioncada, A.; Petrini, R.; Bosio, G.; Gariboldi, K.; Collareta, A.; Malinverno, E.; Bonaccorsi, E.; Di Celma, C.; Pasero, M.; Urbina, M.; Bianucci, G.

    2018-01-01

    The late Miocene Pisco Formation of Peru is an outstanding example of richness and high-quality preservation of fossil marine vertebrates. In order to reconstruct the fossilization path, we present new textural, mineralogical and Sr-isotope data of diagenetic minerals formed in correspondence of fossil specimens such as marine vertebrates and mollusks. These fossil specimens were found at Cerro los Quesos, in the Ica Desert, within the diatomaceous strata of the Pisco Formation. Dolomite, gypsum, anhydrite and Mn minerals are the main phases found, while the calcium carbonate originally forming the mollusk valves is replaced by gypsum. An early formation of dolomite and of Mn minerals, triggered by the modifications of the geochemical environment due to organic matter degradation, is suggested by the textural relationships and is confirmed by the Sr isotopic ratio of dolomite, which agrees with that of seawater at the time of sedimentation. Instead, gypsum Sr isotopic ratios indicate a pre-Miocene seawater-derived brine circulating within the sedimentary sequence as a source for Sr. Oxidation of diagenetic sulfide causing a lowering of the pH of porewater is proposed as an explanation for Ca-carbonate dissolution. The diagenetic chemical environment was, nevertheless, favorable to bone preservation.

  14. Calcium inputs and transport in a base-poor forest ecosystem as interpreted by Sr isotopes

    Treesearch

    Scott W. Bailey; James W. Hornbeck; Charles T. Driscoll; Henri E. Gaudette

    1996-01-01

    Depletion of Ca in forests and its effects on forest health are poorly quantified. Depletion has been difficult to document due to limitations in determining rates at which Ca becomes available for ecosystem processes through weathering, and difficulty in determining changes in ecosystem storage. We coupled a detailed analysis of Sr isotopic composition with a mass...

  15. Sr-Nd-Pb isotope variability across and along the Ecuadorian volcanic arc

    NASA Astrophysics Data System (ADS)

    Ancellin, Marie-Anne; Samaniego, Pablo; Vlastélic, Ivan; Nauret, François; Gannoun, Mouhcine; Hidalgo, Silvana

    2016-04-01

    Determining the contribution of different potential sources in arc magma genesis is of paramount importance for discriminating the role of deep-seated processes at work in the slab and mantle wedge, as well as the process occurring during the magma ascent through the arc crust. The Ecuadorian volcanic arc (2°S - 1°N) results from the subduction of the oceanic Nazca plate below the continental south-American plate. This volcanic province, developed in front of the subducting Carnegie ridge, is characterized by at least 50-60 volcanic centres of Pleistocene-Holocene age, which are distributed along the Western and Eastern Cordilleras and in the back-arc region. Previous studies on this province focused on two main issues: (1) the role of the deep-seated process occurring at the level of the subducting slab and the mantle wedge ([1], [2]), and (2) the role of crustal process ([3]). In this work, we use existing and new (57 samples from 36 volcanoes of the whole Ecuadorian arc) major-trace element and Sr-Nd-Pb isotope data to resolve precisely magma compositional changes occurring across and along the volcanic arc and to precise the role of the heterogeneous crust underlying this arc segment. In the 207Pb/204Pb vs. 206Pb/204Pb diagram, most of Western Cordillera volcanic centres and Back arc volcanoes display a flat trend characterized by a large variation in 206Pb/204Pb (18.5 - 19.15), with little variation in 207Pb/204Pb (15.54-15.62). Along this trend, back arc volcanoes tend towards unradiogenic compositions with Reventador as end-member whereas western cordilleras volcanoes generally show more radiogenic compositions (Pilavo, Imbabura). In contrast, the Eastern cordillera volcanoes display more radiogenic 207Pb/204Pb (15.60 - 15.70) or 208Pb/204Pb (38.7 - 39) at a given 206Pb/204Pb compared to the Western cordillera with similar variation in 206Pb/204Pb (18.85 - 19.05). Extreme compositions are observed at Tungurahua and Antisana volcanoes. Several volcanoes of

  16. Plume-related mantle source of super-large rare metal deposits from the Lovozero and Khibina massifs on the Kola Peninsula, Eastern part of Baltic Shield: Sr, Nd and Hf isotope systematics

    NASA Astrophysics Data System (ADS)

    Kogarko, L. N.; Lahaye, Y.; Brey, G. P.

    2010-03-01

    The two world’s largest complexes of highly alkaline nepheline syenites and related rare metal loparite and eudialyte deposits, the Khibina and Lovozero massifs, occur in the central part of the Kola Peninsula. We measured for the first time in situ the trace element concentrations and the Sr, Nd and Hf isotope ratios by LA-ICP-MS (laser ablation inductively coupled plasma mass spectrometer) in loparite, eudialyte an in some other pegmatitic minerals. The results are in aggreement with the whole rock Sr and Nd isotope which suggests the formation of these superlarge rare metal deposits in a magmatic closed system. The initial Hf, Sr, Nd isotope ratios are similar to the isotopic signatures of OIB indicating depleted mantle as a source. This leads to the suggestion that the origin of these gigantic alkaline intrusions is connected to a deep seated mantle source—possibly to a lower mantle plume. The required combination of a depleted mantle and high rare metal enrichment in the source can be explained by the input of incompatible elements by metasomatising melts/fluids into the zones of alkaline magma generation shortly before the partial melting event (to avoid ingrowth of radiogenic isotopes). The minerals belovite and pyrochlore from the pegmatites are abnormally high in 87Sr /86Sr ratios. This may be explained by closed system isotope evolution as a result of a significant increase in Rb/Sr during the evolution of the peralkaline magma.

  17. Integrated elemental and Sr-Nd-Pb-Hf isotopic studies of Mesozoic mafic dykes from the eastern North China Craton: implications for the dramatic transformation of lithospheric mantle

    NASA Astrophysics Data System (ADS)

    Liu, Shen; Feng, Caixia; Santosh, M.; Feng, Guangying; Coulson, Ian M.; Xu, Mengjing; Guo, Zhuang; Guo, Xiaolei; Peng, Hao; Feng, Qiang

    2018-02-01

    Evolution of the lithospheric mantle beneath the North China Craton (NCC) from its Precambrian cratonic architecture until Paleozoic, and the transformation to an oceanic realm during Mesozoic, with implications on the destruction of cratonic root have attracted global attention. Here we present geochemical and isotopic data on a suite of newly identified Mesozoic mafic dyke swarms from the Longwangmiao, Weijiazhuang, Mengjiazhuang, Jiayou, Huangmi, and Xiahonghe areas (Qianhuai Block) along the eastern NCC with an attempt to gain further insights on the lithospheric evolution of the region. The Longwangmiao dykes are alkaline with LILE (Ba and K)- and LREE-enrichment ((La/Yb) N > 4.3) and EM1-like Sr-Nd-Pb-Hf isotopic signature ((87Sr/86Sr) i > 0.706; ε Nd (t) < -6.3, (206Pb/204Pb) i > 16.6, (207Pb/204Pb) i > 15.4, (208Pb/204Pb) i > 36.8, ε Hf (t) < -22.4). The Weijiazhuang dykes are sub-alkaline with LILE (Ba and K)- and LREE-enrichment ((La/Yb) N > 3.7), and display similar EM1-like isotopic features ((87Sr/86Sr) i > 0.706; ε Nd (t) < -7.0, (206Pb/204Pb) i > 16.7, (207Pb/204Pb) i > 15.4, (208Pb/204Pb) i > 36.9, ε Hf (t) < -23.3). The Mengjiazhuang dykes are also sub-alkaline with LILE (Ba and K)- and LREE-enrichment ((La/Yb) N > 2.4) and EM1-like isotopic features((87Sr/86Sr) i > 0.706; ε Nd (t) < -18.4, (206Pb/204Pb) i > 16.7, (207Pb/204Pb) i > 15.4, (208Pb/204Pb) i > 36.9, ε Hf (t) < -8.6). The Jiayou dykes also display sub-alkaline affinity with LILE (Ba and K)- and LREE-enrichment ((La/Yb) N > 3.7) and EM1-like Sr-Nd-Pb-Hf isotopic features ((87Sr/86Sr) i > 0.706; ε Nd(t) < -15.3, (206Pb/204Pb) i > 16.7, (207Pb/204Pb) i > 15.4, (208Pb/204Pb) i > 36.9, ε Hf (t) < -18.4). The Huangmi dykes are alkaline (with Na2O + K2O ranging to more than 5.9 wt.%)) with LILE (Ba and K)- and LREE-enrichment ((La/Yb) N > 9.3) and EM1-like isotopic composition ((87Sr/86Sr) i > 0.705; ε Nd (t) < -15.1, (206Pb/204Pb) i > 16.9, (207Pb/204Pb) i > 15.5, (208Pb/204Pb) i > 36

  18. Textural and Rb-Sr isotopic evidence for late Paleozoic mylonitization within the Honey Hill fault zone southeastern Connecticut

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    O'Hara, K.D.; Gromet, L.P.

    A petrographic and Rb-Sr isotopic study of rocks within and near the Honey Hill fault zone places important constraints on its history of movement. Rb-Sr apparent ages for micas and plagioclase from these rocks have been reset and range from Permian to Triassic, considerably younger than the minimum stratigraphic age (Ordovician) of the rocks studied or of Acadian (Devonian) regional metamorphism. Permian Rb-Sr ages of dynamically recrystallized muscovite date the development of mylonite fabric. An older age is precluded by the excellent preservation of unrecovered quartz, which indicates that these rocks did not experience temperatures high enough to anneal quartzmore » or thermally reset Rb-Sr isotopic systems in muscovite since the time of mylonitization. Metamorphic mineral assemblages and mineral apparent ages in rocks north of the fault zone indicate recrystallization under similar upper greenschist-lower amphibolite grade conditions during Permian to Triassic time. Collectively these results indicate that the Honey Hill fault zone was active during the Late Paleozoic and that ductile deformation and metamorphism associated with the Alleghanian orogeny extend well into southern Connecticut. An Alleghanian age for mylonitization within the Honey Hill fault zone suggests it should be considered as a possible site for the major Late Paleozoic strike-slip displacements inferred from paleomagnetic studies for parts of coastal New England and maritime Canada.« less

  19. Elemental and isotopic (C, O, Sr, Nd) compositions of Late Paleozoic carbonated eclogite and marble from the SW Tianshan UHP belt, NW China: Implications for deep carbon cycle

    NASA Astrophysics Data System (ADS)

    Zhu, Jianjiang; Zhang, Lifei; Lü, Zeng; Bader, Thomas

    2018-03-01

    Subduction zones are important for understanding of the global carbon cycle from the surface to deep part of the mantle. The processes involved the metamorphism of carbonate-bearing rocks largely control the fate of carbon and contribute to local carbon isotopic heterogeneities of the mantle. In this study, we present petrological and geochemical results for marbles and carbonated eclogites in the Southwestern Tianshan UHP belt, NW China. Marbles are interlayered with coesite-bearing pelitic schists, and have Sr-Nd isotopic values (εNd (T=320Ma) = -3.7 to -8.9, 87Sr/86Sr (i) = 0.7084-0.7089), typical of marine carbonates. The marbles have dispersed low δ18OVSMOW values (ranging from 14 to 29‰) and unaffected carbon isotope (δ13CVPDB = -0.2-3.6‰), possibly due to infiltration of external H2O-rich fluids. Recycling of these marbles into mantle may play a key role in the carbon budget and contributed to the mantle carbon isotope heterogeneity. The carbonated eclogites have high Sr isotopic compositions (87Sr/86Sr (i) = 0.7077-0.7082) and positive εNd (T = 320 Ma) values (from 7.6 to 8.2), indicative of strong seafloor alteration of their protolith. The carbonates in the carbonated eclogites are mainly dolomite (Fe# = 12-43, Fe# = Fe2+/(Fe2+ + Mg)) that were added into oceanic basalts during seafloor alteration and experienced calcite - dolomite - magnesite transformation during the subduction metamorphic process. The uniformly low δ18O values (∼11.44‰) of carbonates in the carbontaed eclogites can be explained by closed-system equilibrium between carbonate and silicate minerals. The low δ13C values (from -3.3 to -7.7‰) of the carbonated eclogites most likely reflect contribution from organic carbon. Recycling of these carbonated eclogites with C isotope similar to typical mantle reservoirs into mantle may have little effect on the mantle carbon isotope heterogeneity.

  20. Towards Time-Scaling of Mixing for the Campanian Ignimbrite: Systemic Variation in Sr-Isotopic Composition from Mixing Experiments

    NASA Astrophysics Data System (ADS)

    de Campos, Cristina; Civetta, Lucia; Perugini, Diego; Dingwell, Donald B.

    2010-05-01

    Eruptions in the Campi Flegrei caldera, the most dangerous volcanic setting in Europe, are thought to be triggered by short-term pre-eruptive mixing of trachytic to trachydacitic resident and new basaltic, trachyandesitic (=shoshonitic) magma, in shallow magma chambers (e. g. Arienzo et al, 2008, Bull. Volcanol.). Previous geochemical and volcanological data on the Campanian Ignimbrite, (>150 km3, 39 Ma), in Campi Flegrei, point towards a layered reservoir, which evolved from the replenishment of the magma chamber with shoshonitic magma and short-term pre-eruptive mixing between a trachytic and a phonolitic trachytic magma. With the purpose to experimentally study the mobility and homogenization of Rb-Sr isotopes in this system, we performed mixing experiments using natural phonolitic trachytic (end-member A - S. Nicola type) and trachytic (end-member B - Mondragone-type) samples, representing the two end-members involved in the origin of the Campanian Ignimbrite. Resultant glasses from a time series, ranging from 1-hour up to 1-week, under constant flow velocity (0.5 rotations per minute; after De Campos et al., 2008. Chem. Geol.), have been analysed with respect to the Rb- and Sr-systematics. Our results reveal a progressive homogenization of the contrasting Sr-isotopes towards a hybrid value. With increasing experimental duration a clear decrease in the standard deviation of isotopic ratios has been observed, reflecting progressive isotopic homogenization. Our results also support the effectiveness of mixing in the Campi Flegrei reservoirs, in liquidus, under high temperature, before the onset of fractional crystallization. Since different eruptive events from Campi Flegrei can be well characterized by means of isotopic composition, the main goal for the present study will be to use experimental data and numerical modeling in order to estimate time scales of mixing associated with the eruption of the Campanian Ignimbrite, and then compare them to the several

  1. The 87Sr/86Sr aquatic isoscape of the Danube catchment from the source to the mouth as tool for studying fish migrations

    NASA Astrophysics Data System (ADS)

    Zitek, Andreas; Tchaikovsky, Anastassiya; Irrgeher, Johanna; Waidbacher, Herwig; Prohaska, Thomas

    2014-05-01

    Isoscapes - spatially distributed isotope patterns across landscapes - are increasingly used as important basis for ecological studies. The natural variation of the isotopic abundances in a studied area bears the potential to be used as natural tracer for studying e.g. migrations of animals or prey-predator relations. The 87Sr/86Sr ratio is one important tracer, since it is known to provide a direct relation of biological samples to geologically distinct regions, as Sr isotopes are incorporated into living tissues as a proxy for calcium and taken up from the environment without any significant fractionation. Although until now the focus has been mainly set on terrestrial systems, maps for aquatic systems are increasingly being established. Here we present the first 87Sr/86Sr aquatic isoscape of the Danube catchment, the second largest river catchment in Europe, from near its source starting at river km 2581 in Germany down to its mouth to river km 107 in Romania. The total length of the river Danube is 2780 km draining a catchment area 801 463 km2 (10 % of the European continent). The major purpose of this study was to assess the potential of the 87Sr/86Sr isotope ratio to be used as tool for studying fish migrations at different scales in the entire Danube catchment. Within the Joint Danube Research 3 (JDS 3), the biggest scientific multi-disciplinary river expedition of the World in 2013 aiming at the assessment of the ecological status and degree of human alterations along the river Danube, water samples were taken at 68 pre-defined sites along the course of the river Danube including the major tributaries as a basis to create the so called 'Isoscape of the Danube catchment'. The determination of 87Sr/86Sr isotope ratio in river water was performed by multicollector-sector field-inductively coupled plasma-mass spectrometry (MC-SF-ICP-MS). The JDS 3 data were combined with existing data from prior studies conducted within the Austrian part of the Danube catchment

  2. Isotope pattern deconvolution as rising tool for isotope tracer studies in environmental research

    NASA Astrophysics Data System (ADS)

    Irrgeher, Johanna; Zitek, Andreas; Prohaska, Thomas

    2014-05-01

    During the last decade stable isotope tracers have emerged as versatile tool in ecological research. Besides 'intrinsic' isotope tracers caused by the natural variation of isotopes, the intentional introduction of 'extrinsic' enriched stable isotope tracers into biological systems has gained significant interest. Hereby the induced change in the natural isotopic composition of an element allows amongst others for studying the fate and fluxes of metals, trace elements and species in organisms or provides an intrinsic marker or tag of particular biological samples. Due to the shoreless potential of this methodology, the number of publications dealing with applications of isotope (double) spikes as tracers to address research questions in 'real world systems' is constantly increasing. However, some isotope systems like the natural Sr isotopic system, although potentially very powerful for this type of application, are still rarely used, mainly because their adequate measurement/determination poses major analytical challenges; as e.g. Sr is available in significant amounts in natural samples. In addition, biological systems underlie complex processes such as metabolism, adsorption/desorption or oxidation/reduction. As a consequence, classic evaluation approaches such as the isotope dilution mass spectrometry equation are often not applicable because of the unknown amount of tracer finally present in the sample. Isotope pattern deconvolution (IPD), based on multiple linear regression, serves as simplified alternative data processing strategy to double spike isotope dilution calculations. The outstanding advantage of this mathematical tool lies in the possibility of deconvolving the isotope pattern in a spiked sample without knowing the quantities of enriched isotope tracer being incorporated into the natural sample matrix as well as the degree of impurities and species-interconversion (e.g. from sample preparation). Here, the potential of IPD for environmental tracer

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

    NASA Astrophysics Data System (ADS)

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

    2012-12-01

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

  4. High-precision Al-Mg isotopic systematics in USNM 3898 - The benchmark "ALL" for initial 87Sr/86Sr in the earliest Solar System

    NASA Astrophysics Data System (ADS)

    MacPherson, G. J.; Defouilloy, C.; Kita, N. T.

    2018-06-01

    The Allende CAI USNM 3898 is the basis for "ALL", the lowest measured initial 87Sr/86Sr value in any solar system material including other CAIs (Gray et al., 1973). If the value ALL is correct (debated), then USNM 3898 must be 1-2 million years older than other CAIs (Podosek et al., 1991). This would require in turn that it have a much higher initial 26Al/27Al value than other CAIs, on the order of 4 × 10-4. Podosek et al. (1991) showed that this is not the case, with initial 26Al/27Al = (4.5 ± 0.7) × 10-5, but their Mg-isotopic data had large error bars and there was clear isotopic disturbance in the data having the highest 27Al/24Mg. Without the latter data, the slope of their isochron is higher (5.10 ± 1.19) × 10-5) and within (large) error of being supracanonical. We used high-precision SIMS to re-determine the initial 26Al/27Al in this CAI and obtained a value of (5.013 ± 0.099) × 10-5, with an intercept δ26Mg* = - 0.008 ± 0.048 and MSWD = 1.3. This value is indistinguishable from that measured in many other CAIs and conclusively shows that USNM 3898 is not uniquely ancient. We also confirmed evidence of later isotopic disturbance, similar to what Podosek et al. found, indicating a re-melting and evaporation event some 200,000 years after initial CAI solidification.

  5. Effect of Bioaccumulation of Cs and Sr Natural Isotopes on Foliar Structure and Plant Spectral Reflectance of Indian Mustard (Brassica juncea)

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Maruthi Sridhar, Y.S.B.B.; Han, F.X.; Monts, D.L.

    2008-07-01

    The objectives of this study are: 1.) evaluate the capacity of Indian mustard (Brassica juncea) for uptake and accumulation of Cs and Sr natural isotopes; 2.) identify foliar structural and other physiological changes (biomass, relative water content, etc.) resulting from the accumulation of these two elements; and 3.) monitor Cs and Sr uptake and bioaccumulation process by spectral reflectance. Potted Indian mustard plants were exposed to different concentrations of Cs (50 and 600 ppm) and Sr (50 and 300 ppm) natural isotopes in solution form for 23 days. Bioaccumulation of Cs and Sr was found in the order of leavesmore » > stems > roots for both Cs- and Sr-treated plants. The highest leaf Sr accumulation is observed to be 2708 mg kg{sup -1}, and the highest leaf Cs accumulation is 12251 mg kg{sup -1}. High translocation efficiency for both elements is documented by shoot/root concentration ratios greater than one. Relative water content (RWC) of the plants showed a significant (p < 0.05) decrease in Cs-treated plants. Cs accumulation also affected the pigment concentration and internal structure of the leaf and the spectral characteristics of plants. Within the applied concentration range, Sr accumulation resulted in no significant changes in RWC, structural and spectral characteristics of mustard plants. Cs shoot concentration showed significant negative correlation with relative water content RWC (r = -0.88) and Normalized Difference Vegetation Index (NDVI) (r = -0.68) of plant shoots. The canopy spectral reflectance and NDVI analysis clearly revealed (p < 0.05) the stress caused by Cs accumulation. (authors)« less

  6. The Origin of 87Sr/86Sr in Cold Springs and Travertines of the Franciscan Complex near Cazadero, California

    NASA Astrophysics Data System (ADS)

    Marks, N.; Schiffman, P.; Yin, Q.; Zierenberg, R.

    2005-12-01

    Ultrabasic springs within the Franciscan Complex of the California Coast Range have been intensely investigated by geochemists and geobiologists. Springs located in Sonoma County in an area historically known as The Cedars are of particular interest to scientists exploring Martian analogues (Johnson et al. 2004) or investigating serpentinization processes (Barnes and O'Neil, 1969; Barnes et al. 1972). Laser ablation and solution phase multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) were used to obtain 87Sr/86Sr isotope ratios in fluid, travertine and serpentinite samples collected at the Cedars. 87Sr/86Sr isotopic ratios in the serpentinizing springs range from 0.70926 to 0.70955; the Mg2+-HCO3- type stream water has an isotopic ratio of 0.70848. The 87Sr/86Sr ratio in the travertines ranges from 0.70931 to 0.70966. The mean 87Sr/86Sr ratio of the travertine (0.7094) is far more radiogenic than typical mantle values of 0.703 to 0.705, indicating that the peridotite is an unlikely source of the radiogenic Sr. Similarly, the measured ratio is much higher than the expected Sr isotope ratio of seawater that might be trapped in Jurassic Franciscan Sediments or oceanic crust. Strontium leached from Franciscan sediments themselves should reflect a Sierran or Klamath source with expected values in the range of 0.705 to 0.706. Indeed the measured isotope ratios even exceed modern seawater values. The observed radiogenic values suggest the presence of older, potassium (and rubidium)-rich rocks within the fluid flow path. Alternatively, the presence of clay minerals that readily substitute Sr for Ca may well account for the radiogenic strontium signal. It is possible that the serpentinization observed at The Cedars initiated along a ridge flank and the Sr isotopic chemistry reflects the site of initiation. The radiogenic strontium in these springs may result from fluid interaction with seafloor sediments deposited along the flank of a slow spreading

  7. Multiple isotopes (O, C, Li, Sr) as tracers of CO2 and brine leakage from CO2-enhanced oil recovery activities in Permian Basin, Texas, USA

    NASA Astrophysics Data System (ADS)

    Phan, T. T.; Sharma, S.; Gardiner, J. B.; Thomas, R. B.; Stuckman, M.; Spaulding, R.; Lopano, C. L.; Hakala, A.

    2017-12-01

    Potential CO2 and brine migration or leakage into shallow groundwater is a critical issue associated with CO2 injection at both enhanced oil recovery (EOR) and carbon sequestration sites. The effectiveness of multiple isotope systems (δ18OH2O, δ13C, δ7Li, 87Sr/86Sr) in monitoring CO2 and brine leakage at a CO2-EOR site located within the Permian basin (Seminole, Texas, USA) was studied. Water samples collected from an oil producing formation (San Andres), a deep groundwater formation (Santa Rosa), and a shallow groundwater aquifer (Ogallala) over a four-year period were analyzed for elemental and isotopic compositions. The absence of any change in δ18OH2O or δ13CDIC values of water in the overlying Ogallala aquifer after CO2 injection indicates that injected CO2 did not leak into this aquifer. The range of Ogallala water δ7Li (13-17‰) overlaps the San Andres water δ7Li (13-15‰) whereas 87Sr/86Sr of Ogallala (0.70792±0.00005) significantly differs from San Andres water (0.70865±0.00003). This observation demonstrates that Sr isotopes are much more sensitive than Li isotopes in tracking brine leakage into shallow groundwater at the studied site. In contrast, deep groundwater δ7Li (21-25‰) is isotopically distinct from San Andres produced water; thus, monitoring this intermitted formation water can provide an early indication of CO2 injection-induced brine migration from the underlying oil producing formation. During water alternating with gas (WAG) operations, a significant shift towards more positive δ13CDIC values was observed in the produced water from several of the San Andres formation wells. The carbon isotope trend suggests that the 13C enriched injected CO2 and formation carbonates became the primary sources of dissolved inorganic carbon in the area surrounding the injection wells. Moreover, one-way ANOVA statistical analysis shows that the differences in δ7Li (F(1,16) = 2.09, p = 0.17) and 87Sr/86Sr (F(1,18) = 4.47, p = 0.05) values of

  8. Homogeneous impact melts produced by a heterogeneous target?. Sr-Nd isotopic evidence from the Popigai crater, Russia

    NASA Astrophysics Data System (ADS)

    Kettrup, B.; Deutsch, A.; Masaitis, V. L.

    The 35.7 ± 0.2 Ma old Popigai crater, Siberia, with a diameter of about 100 km is one of the best preserved large terrestrial impact structures. The heterogeneous target at the impact site consists of Archean to Lower Proterozoic metamorphic rocks of the crystalline basement, Upper Proterozoic quartzites and other clastic deposits, as well as Cambrian to Cretaceous clastic sediments and sedimentary rocks, including carbonate rocks. Moreover, Proterozoic and Permo-Triassic dolerite dykes are found in the target area. We report major element, Sr and Nd isotope data for 13 of these target rocks and for various types of impactites. The 15 analysed impactite samples include tagamites (impact melt rocks), suevites and impact glass from small veins. Furthermore, two impact breccias and two impact glass-coated gneiss bombs were analysed. We discuss the relation of these impactites to the target lithologies, and evaluate on the basis of literature data the relation of microkrystites (and associated microtektites) in Upper Eocene sediments to the Popigai event. The impactites have SiO 2 abundances ranging from 59 to 66 wt.% and show significant variations in the content of Fe, Ca, and Ti. They have present day 87Sr/ 86Sr ratios between 0.7191 and 0.7369. Their Sr model ages T SrUR range from 1.9 to 2.3 Ga. The 143Nd/ 144Nd ratios for the impactite samples cluster between 0.5113 and 0.5115. The Nd model ages T NdCHUR range from 1.9 to 2.1 Ga. In an ɛ CHUR(Nd)-ɛ UR(Sr) diagram, the impactites and Upper Eocene microkrystites (and associated microtektites) plot in a field delimited by Popigai target lithologies. The impactites are restricted to the field of crystalline basement rocks and Upper Proterozoic quartzites, but they show different isotopic signatures in different crater sectors. Impactites and Upper Eocene microkrystites plot in different, only partly overlapping clusters. The leucocratic microkrystites and microtektites have a higher affinity to the post

  9. Ion microprobe measurement of strontium isotopes in calcium carbonate with application to salmon otoliths

    USGS Publications Warehouse

    Weber, P.K.; Bacon, C.R.; Hutcheon, I.D.; Ingram, B.L.; Wooden, J.L.

    2005-01-01

    The ion microprobe has the capability to generate high resolution, high precision isotopic measurements, but analysis of the isotopic composition of strontium, as measured by the 87Sr/ 86Sr ratio, has been hindered by isobaric interferences. Here we report the first high precision measurements of 87Sr/ 86Sr by ion microprobe in calcium carbonate samples with moderate Sr concentrations. We use the high mass resolving power (7000 to 9000 M.R.P.) of the SHRIMP-RG ion microprobe in combination with its high transmission to reduce the number of interfering species while maintaining sufficiently high count rates for precise isotopic measurements. The isobaric interferences are characterized by peak modeling and repeated analyses of standards. We demonstrate that by sample-standard bracketing, 87Sr/86Sr ratios can be measured in inorganic and biogenic carbonates with Sr concentrations between 400 and 1500 ppm with ???2??? external precision (2??) for a single analysis, and subpermil external precision with repeated analyses. Explicit correction for isobaric interferences (peak-stripping) is found to be less accurate and precise than sample-standard bracketing. Spatial resolution is ???25 ??m laterally and 2 ??m deep for a single analysis, consuming on the order of 2 ng of material. The method is tested on otoliths from salmon to demonstrate its accuracy and utility. In these growth-banded aragonitic structures, one-week temporal resolution can be achieved. The analytical method should be applicable to other calcium carbonate samples with similar Sr concentrations. Copyright ?? 2005 Elsevier Ltd.

  10. Kinetics of the reaction of the heaviest hydrogen atom with H2, the 4Heμ + H2 → 4HeμH + H reaction: Experiments, accurate quantal calculations, and variational transition state theory, including kinetic isotope effects for a factor of 36.1 in isotopic mass

    NASA Astrophysics Data System (ADS)

    Fleming, Donald G.; Arseneau, Donald J.; Sukhorukov, Oleksandr; Brewer, Jess H.; Mielke, Steven L.; Truhlar, Donald G.; Schatz, George C.; Garrett, Bruce C.; Peterson, Kirk A.

    2011-11-01

    The neutral muonic helium atom 4Heμ, in which one of the electrons of He is replaced by a negative muon, may be effectively regarded as the heaviest isotope of the hydrogen atom, with a mass of 4.115 amu. We report details of the first muon spin rotation (μSR) measurements of the chemical reaction rate constant of 4Heμ with molecular hydrogen, 4Heμ + H2 → 4HeμH + H, at temperatures of 295.5, 405, and 500 K, as well as a μSR measurement of the hyperfine coupling constant of muonic He at high pressures. The experimental rate constants, kHeμ, are compared with the predictions of accurate quantum mechanical (QM) dynamics calculations carried out on a well converged Born-Huang (BH) potential energy surface, based on complete configuration interaction calculations and including a Born-Oppenheimer diagonal correction. At the two highest measured temperatures the agreement between the quantum theory and experiment is good to excellent, well within experimental uncertainties that include an estimate of possible systematic error, but at 295.5 K the quantum calculations for kHeμ are below the experimental value by 2.1 times the experimental uncertainty estimates. Possible reasons for this discrepancy are discussed. Variational transition state theory calculations with multidimensional tunneling have also been carried out for kHeμ on the BH surface, and they agree with the accurate QM rate constants to within 30% over a wider temperature range of 200-1000 K. Comparisons between theory and experiment are also presented for the rate constants for both the D + H2 and Mu + H2 reactions in a novel study of kinetic isotope effects for the H + H2 reactions over a factor of 36.1 in isotopic mass of the atomic reactant.

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  12. 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

    USGS Publications Warehouse

    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.

  13. Anomalous isotopic compositions of Sr, Ar and O in the Mesozoic diabase dikes of Liberia, West Africa

    NASA Astrophysics Data System (ADS)

    Mauche, Renée; Faure, Gunter; Jones, Lois M.; Hoefs, Jochen

    1989-01-01

    The Mesozoic diabase dikes of Liberia are tholeiites whose 87Sr/86Sr and 87Rb/86Sr ratios scatter widely on the Rb-Sr isochron diagram. The problem is attributed to differences in the initial 87Sr/86Sr ratios of these rocks which range from 0.70311 to 0.70792, assuming a uniform age of 186 Ma for the dikes and using λ(87Rb)=1.42 × 10-11y-1. The range of values is similar to that observed in the Mesozoic basalt flows and dikes of other Gondwana continents. New whole-rock K-Ar dates confirm previous conclusions that the diabase dikes in the Liberian and Pan-African age provinces of Liberia absorbed extraneous 40Ar after intrusion. Only the dikes in the Paynesville Sandstone have K-Ar dates that range from 117 Ma to 201 Ma and may not contain extraneous 40Ar. However, dikes from all three age provinces of Liberia have elevated initial 87Sr/86Sr ratios. These results indicate that contamination with radiogenic 87Sr occurred primarily before intrusion of the magma whereas the addition of extraneous 40Ar occurred after emplacement and reflects the age and mineral composition of the country rock. The δ 18O values of the Liberian diabase range from +5.6/% to +9.10/% and correlate positively with initial 87Sr/86Sr ratios. The data can be modeled by fractional crystallization and simultaneous assimilation of crustal rocks by the magma. However, samples containing amphibole and biotite replacing pyroxene deviate from the Sr-O isotope trajectories of the model and appear to have been depleted in 18O and enriched in 87Sr by interactions with groundwater at high temperature.

  14. Subduction and melting processes inferred from U-Series, Sr Nd Pb isotope, and trace element data, Bicol and Bataan arcs, Philippines

    NASA Astrophysics Data System (ADS)

    DuFrane, S. Andrew; Asmerom, Yemane; Mukasa, Samuel B.; Morris, Julie D.; Dreyer, Brian M.

    2006-07-01

    We present U-series, Sr-Nd-Pb isotope, and trace element data from the two principal volcanic chains on Luzon Island, developed over oppositely dipping subduction zones, to explore melting and mass transfer processes beneath arcs. The Bataan (western) and Bicol (eastern) arcs are currently subducting terrigenous and pelagic sediments, respectively, which have different trace element and isotopic compositions. The range of ( 230Th/ 238U) disequilibria for both arcs is 0.85-1.15; only lavas from Mt. Mayon (Bicol arc) have 230Th activity excesses. Bataan lavas have higher 87Sr/ 86Sr and lower 143Nd/ 144Nd than Bicol lavas ( 87Sr/ 86Sr = 0.7042-0.7046, 143Nd/ 144Nd = 0.51281-0.51290 vs. 87Sr/ 86Sr = 0.70371-0.70391, 143Nd/ 144Nd = 0.51295-0.51301) and both arcs show steep linear arrays towards sediment values on 207Pb/ 204Pb vs. 206Pb/ 204Pb diagrams. Analysis of incompatible element and isotopic data allows identification of a sediment component that, at least in part, was transferred as a partial melt to the mantle wedge peridotite. Between 1% and 5% sediment melt addition can explain the isotopic and trace element variability in the rocks from both arcs despite the differences in sediment supply. We therefore propose that sediment transfer to the mantle wedge is likely mechanically or thermally limited. It follows that most sediments are either accreted, reside in the sub-arc lithosphere, or are recycled into the convecting mantle. However, whole-sale sediment recycling into the upper mantle is unlikely in light of the global mid-ocean ridge basalt data. Fluid involvement is more difficult to characterize, but overall the Bicol arc appears to have more fluid influence than the Bataan arc. Rock suites from each arc can be related by a dynamic melting process that allows for 230Th ingrowth, either by dynamic or continuous flux melting, provided the initial ( 230Th/ 232Th) of the source is ˜0.6-0.7. The implication of either model is that inclined arrays on the U

  15. The geochemical and Sr-Nd-Pb-He isotopic characterization of the mantle source of Rungwe Volcanic Province: comparison with the Afar mantle domain

    NASA Astrophysics Data System (ADS)

    Castillo, P. R.; Hilton, D. R.; Halldorsson, S. A.; Wang, R.

    2012-12-01

    The ultimate source of heat and magmatism associated with continental rifting in the East African Rift System (EARS) is generally viewed to be the African Superplume, but there is continuing debate on the surface expression of this large anomalous feature, which originates in the lower mantle. Previous studies have demonstrated an insignificant role for crustal contamination thereby identifying a single mantle plume signature in Quaternary basalts from the Main Ethiopian Rift in the northern EARS. This is designated to be the Afar plume and is characterized by, e.g., 3He/4He >15 RA, 206Pb/204Pb = 19.5 and 87Sr/86Sr = 0.7035 [Rooney et al., J. Pet. 53, 2012]. In contrast, the signature of plume(s) in the southern EARS is less constrained. Rogers et al. [EPSL 176, 2000] proposed a plume in the sub-lithospheric Kenyan mantle with characteristically lower 43Nd/144Nd than the Afar plume whereas Furman [JAES 48, 2007] advocated a high μ [HIMU] plume based primarily on the high 206Pb/204Pb ratios of lavas in all areas within and south of the Turkana Depression: both models assume a 3He/4He lower than the Afar plume. Here we report the trace element and Sr-Nd-Pb isotopic composition of basaltic lavas from the Rungwe Volcanic Province (RVP) in the southern extreme of the Western Rift previously identified as a high 3He/4He locality (~15 RA; [Hilton et al., GRL 38, 2011]). Trace element analyses are within the previously reported range of lava compositions that include a relatively large lithospheric component. More importantly, we identify correlations among incompatible trace element and isotopic ratios (e.g., 3He/4He vs 206Pb/204Pb, Rb/Sr, Nb/Ta; 87Sr/86Sr vs 208Pb/204Pb). Our new results suggest the presence of a distinct, high 3He/4He mantle source beneath RVP that is more radiogenic (e.g., 206Pb/204Pb up to ~19.8; 87Sr/86Sr up to 0.7055) than the Afar mantle plume. There is also very little or no HIMU signature in RPV basalts based on their high Sr and low Nd isotopic

  16. Using stable isotopes (δD, δ18O, δ34S and 87Sr/86Sr) to identify sources of water in abandoned mines in the Fengfeng coal mining district, northern China

    NASA Astrophysics Data System (ADS)

    Qu, Shen; Wang, Guangcai; Shi, Zheming; Xu, Qingyu; Guo, Yuying; Ma, Luan; Sheng, Yizhi

    2018-05-01

    With depleted coal resources or deteriorating mining geological conditions, some coal mines have been abandoned in the Fengfeng mining district, China. Water that accumulates in an abandoned underground mine (goaf water) may be a hazard to neighboring mines and impact the groundwater environment. Groundwater samples at three abandoned mines (Yi, Er and Quantou mines) in the Fengfeng mining district and the underlying Ordovician limestone aquifer were collected to characterize their chemical and isotopic compositions and identify the sources of the mine water. The water was HCO3·SO4-Ca·Mg type in Er mine and the auxiliary shaft of Yi mine, and HCO3·SO4-Na type in the main shaft of Quantou mine. The isotopic compositions (δD and δ18O) of water in the three abandoned mines were close to that of Ordovician limestone groundwater. Faults in the abandoned mines were developmental, possibly facilitating inflows of groundwater from the underlying Ordovician limestone aquifers into the coal mines. Although the Sr2+ concentrations differed considerably, the ratios of Sr2+/Ca2+ and 87Sr/86Sr and the 34S content of SO4 2- were similar for all three mine waters and Ordovician limestone groundwater, indicating that a close hydraulic connection may exist. Geochemical and isotopic indicators suggest that (1) the mine waters may originate mainly from the Ordovician limestone groundwater inflows, and (2) the upward hydraulic gradient in the limestone aquifer may prevent its contamination by the overlying abandoned mine water. The results of this study could be useful for water resources management in this area and other similar mining areas.

  17. Recoil Distance Method lifetime measurement of the 2 1 + state in 94Sr and implications for the structure of neutron rich Sr isotopes

    NASA Astrophysics Data System (ADS)

    Chester, Aaron; Starosta, Krzysztof; S1467 Experiment Collaboration

    2017-09-01

    A high precision lifetime measurement of the 21+ state in 94Sr was performed at TRIUMF's ISAC-II facility by coupling the Recoil Distance Method implemented via the TIGRESS Integrated Plunger with unsafe Coulomb excitation in inverse kinematics. Due to limited statistics imposed by the use of a radioactive 94Sr beam, a likelihood ratio χ2 method was derived and used to compare experimental data to Geant4-simulated lineshapes. The B (E 2 ;21+ ->01+) value extracted from the lifetime measurement of 7 .80-0.40 + 0.50 (stat .) +/- 0.07 (sys .) ps is approximately 25% larger than previously reported while the relative uncertainty has been reduced by a factor of approximately 8. A baseline deformation has been established for Sr isotopes with N <= 58 which is a necessary condition for the Quantum Phase Transition interpretation of the onset of deformation in this region. A summary of the experiment, description of the data analysis methods, and a comparison to existing theoretical models will be presented.

  18. Slab-derived components in the subcontinental lithospheric mantle beneath Chilean Patagonia: Geochemistry and Sr-Nd-Pb isotopes of mantle xenoliths and host basalt

    NASA Astrophysics Data System (ADS)

    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

  19. Determination of plutonium isotopes (238,239,240Pu) and strontium (90Sr) in seafood using alpha spectrometry and liquid scintillation spectrometry.

    PubMed

    Shin, Choonshik; Choi, Hoon; Kwon, Hye-Min; Jo, Hye-Jin; Kim, Hye-Jeong; Yoon, Hae-Jung; Kim, Dong-Sul; Kang, Gil-Jin

    2017-10-01

    The present study was carried out to survey the levels of plutonium isotopes ( 238 , 239 , 240 Pu) and strontium ( 90 Sr) in domestic seafood in Korea. In current, regulatory authorities have analyzed radionuclides, such as 134 Cs, 137 Cs and 131 I, in domestic and imported food. However, people are concerned about contamination of other radionuclides, such as plutonium and strontium, in food. Furthermore, people who live in Korea have much concern about safety of seafood. Accordingly, in this study, we have investigated the activity concentrations of plutonium and strontium in seafood. For the analysis of plutonium isotopes and strontium, a rapid and reliable method developed from previous study was used. Applicability of the test method was verified by examining recovery, minimum detectable activity (MDA), analytical time, etc. Total 40 seafood samples were analyzed in 2014-2015. As a result, plutonium isotopes ( 238 , 239 , 240 Pu) and strontium ( 90 Sr) were not detected or below detection limits in seafood. The detection limits of plutonium isotopes and strontium-90 were 0.01 and 1 Bq/kg, respectively. Copyright © 2017 Elsevier Ltd. All rights reserved.

  20. Rb-Sr isotopic studies of postorogenic granites from the eastern Arabian Shield, Kingdom of Saudi Arabia

    USGS Publications Warehouse

    Stuckless, J.S.; Futa, Kiyoto

    1987-01-01

    Available data indicate that postorogenic granites tend to be older in the southern part of the Arabian Shield. This suggests that plutonism started in the south and progressed to the north. Initial 87Sr/86Sr values also form a regional pattern. These ratios tend to be higher in the eastern part of the Arabian Shield, and suggest one source of continental affinity to the east and one of oceanic affinity to the west. The distribution of initial strontium isotope ratios does not clearly discriminate between the various models for Shield evolution; however, a sedimentary source region of mixed end members seems more compatible with the data pattern than models based on discrete boundaries between unrelated accreted blocks.

  1. Repeated kimberlite magmatism beneath Yakutia and its relationship to Siberian flood volcanism: Insights from in situ U-Pb and Sr-Nd perovskite isotope analysis

    NASA Astrophysics Data System (ADS)

    Sun, Jing; Liu, Chuan-Zhou; Tappe, Sebastian; Kostrovitsky, Sergey I.; Wu, Fu-Yuan; Yakovlev, Dmitry; Yang, Yue-Heng; Yang, Jin-Hui

    2014-10-01

    We report combined U-Pb ages and Sr-Nd isotope compositions of perovskites from 50 kimberlite occurrences, sampled from 9 fields across the Yakutian kimberlite province on the Siberian craton. The new U-Pb ages, together with previously reported geochronological constraints, suggest that kimberlite magmas formed repeatedly during at least 4 episodes: Late Silurian-Early Devonian (419-410 Ma), Late Devonian-Early Carboniferous (376-347 Ma), Late Triassic (231-215 Ma), and Middle/Late Jurassic (171-156 Ma). Recurrent kimberlite melt production beneath the Siberian craton - before and after flood basalt volcanism at 250 Ma - provides a unique opportunity to test existing models for the origin of global kimberlite magmatism. The internally consistent Sr and Nd isotope dataset for perovskites reveals that the Paleozoic and Mesozoic kimberlites of Yakutia have distinctly different initial radiogenic isotope compositions. There exists a notable increase in the initial 143Nd/144Nd ratios through time, with an apparent isotopic evolution that is intermediate between that of Bulk Earth and Depleted MORB Mantle. While the Paleozoic samples range between initial 87Sr/86Sr of 0.7028-0.7034 and 143Nd/144Nd of 0.51229-0.51241, the Mesozoic samples show values between 0.7032-0.7038 and 0.51245-0.51271, respectively. Importantly, perovskites from all studied Yakutian kimberlite fields and age groups have moderately depleted initial εNd values that fall within a relatively narrow range between +1.8 and +5.5. The perovskite isotope systematics of the Yakutian kimberlites are interpreted to reflect magma derivation from the convecting upper mantle, which appears to have a record of continuous melt depletion and crustal recycling throughout the Phanerozoic. The analyzed perovskites neither record highly depleted nor highly enriched isotopic components, which had been previously identified in likely plume-related Siberian Trap basalts. The Siberian craton has frequently been suggested

  2. Geochemical and isotopic (Nd-Pb-Sr-O) variations bearing on the genesis of volcanic rocks from Vesuvius, Italy

    USGS Publications Warehouse

    Ayuso, R.A.; de Vivo, B.; Rolandi, G.; Seal, R.R.; Paone, A.

    1998-01-01

    commonly seen in rocks generated at orogenic margins are absent in our samples. Sr isotopic compositions are known to be variable within some of the units, in agreement with our data (87Sr/86Sr ~ 0.70699 to 0.70803) and with contributions from several isotopic components. Isotopic compositions for ??18O (7.3 to 10.2%), Pb for mineral separates and whole rocks (206Pb/204Pb ~ 18.947 to 19.178, 207Pb/204/Pb ~ 15.617 to 15.769, 208Pb/204Pb ~38.915 to 39.345), and Nd (143Nd ~ 0.51228 to 0.51251) also show variability. Oxygen isotope data show that pumices have higher ??18O values than cogenetic lavas, and that ??18O values and SiO2 are correlated. Radiogenic and stable isotope data plot within range of isotopic compositions for the Roman comagmatic province. Fractional crystallization cannot account for the radiogenic isotopic compositions of the Vesuvius magmas. We favor instead the combined effects of heterogeneous magma sources, together with isotopic exchange near the roof of the magma chamber. We suggest that metasomatized continental mantle lithosphere is the principal source of the magmas. This kind of enriched mantle was melted and reactivated in an area of continental extension (incipient rift setting) without direct reliance on contemporaneous subduction processes but possibly with input from mantle sources that resemble those that produce ocean island basalts.

  3. Ca biogeochemical cycle at the beech tree - soil solution interface from the Strengbach CZO (NE France): a clue from stable Ca and radiogenic Sr isotopes

    NASA Astrophysics Data System (ADS)

    Schmitt, Anne-Désirée; Gangloff, Sophie; Labolle, François; Chabaux, François; Stille, Peter

    2017-04-01

    Stable calcium and radiogenic Sr are analysed in several organs from two beech trees that were collected in June and September in the Strengbach CZO (NE France) and in corresponding soil solutions. The combination of these two isotopic systems shows that the isotopic signatures of roots are dominated by Ca fractionation mechanisms and Sr, and thus Ca, source variations. In contrast, translocation mechanisms are only governed by Ca fractionation processes. This study also confirms in the field that the Ca uptake mechanisms from nutritive solutions are controlled by adsorption processes in small roots because of physico-chemical mechanisms. Similarly, a study of surface soil solutions suggests that recent soil waters are less affected by vegetation uptake than in the past, probably because of a decline in the growth of the vegetation that is linked to climate warming, which causes drought episodes. Thus, soil solutions reflect the role of soil components in addition to nutrient uptake by vegetation. This isotopic Ca-Sr study also helps to identify one-time events that are caused by snow cover melting and/or dry episodes that release cations.

  4. Provenance of cryoconite deposited on the glaciers of the Tibetan Plateau: New insights from Nd-Sr isotopic composition and size distribution

    NASA Astrophysics Data System (ADS)

    Dong, Zhiwen; Kang, Shichang; Qin, Dahe; Li, Yang; Wang, Xuejia; Ren, Jiawen; Li, Xiaofei; Yang, Jiao; Qin, Xiang

    2016-06-01

    This study presents the Nd-Sr isotopic compositions and size distributions of cryoconite deposited on the glaciers at different locations on the Tibetan Plateau, in order to trace its source areas and the provenance of long-range transported (LRT) Asian dust on the Tibetan Plateau. The result of scanning electron microscope-energy dispersive X-ray spectrometer analysis indicated that mineral dust particles were dominant in the cryoconite. Most of the cryoconite samples from the Tibetan Plateau indicated different Sr and Nd isotopic composition compared with sand from large deserts (e.g., the Taklimakan and Qaidam deserts). Some cryoconite samples showed very similar Nd-Sr isotopic ratios compared with those of nearby glacier basins (e.g., at Laohugou Glacier No.12, Dongkemadi Glacier, and Shiyi Glacier), indicating the potential input of local crustal dust to cryoconite. The volume-size distribution for the cryoconite particles also indicated bimodal distribution graphs with volume median diameters ranging from 0.57 to 20 µm and from 20 to 100 µm, demonstrating the contribution of both LRT Asian dust and local dust inputs to cryoconite. Based on the particle size distribution, we calculated a mean number ratio of local dust contribution to cryoconite ranging from 0.7% (Baishui Glacier No.1) to 17.6% (Shiyi Glacier) on the Tibetan Plateau. In general, the marked difference in the Nd-Sr isotopic ratios of cryoconite compared with those of large deserts probably indicates that materials from the western deserts have not been easily transported to the hinterland of Tibetan Plateau by the Westerlies under the current climatic conditions, and the arid deserts on the Tibetan Plateau are the most likely sources for cryoconite deposition. The resistance of the Tibetan Plateau to the Westerlies may have caused such phenomena, especially for LRT eolian dust transported over the Tibetan Plateau. Thus, this work is of great importance in understanding the large-scale eolian

  5. Provenance of cryoconite deposited on the glaciers of the Tibetan Plateau: new insights from Nd-Sr isotopic composition and size distribution

    NASA Astrophysics Data System (ADS)

    Dong, Z.

    2016-12-01

    This study presents the Nd-Sr isotopic compositions and size distributions of cryoconite deposited on the glaciers at different locations on the Tibetan Plateau, in order to trace its source areas and the provenance of long-range transported (LRT) Asian dust on the Tibetan Plateau. The result of SEM-EDS analysis indicated that mineral dust particles were dominant in the cryoconite. Most of the cryoconite samples from the Tibetan Plateau indicated different Sr and Nd isotopic composition compared with sand from large deserts (e.g., the Taklimakan and Qaidam deserts). Some cryoconite samples showed very similar Nd-Sr isotopic ratios compared with those of nearby glacier basins (e.g., at Laohugou Glacier No.12, Dongkemadi Glacier and Shiyi Glacier), indicating the potential input of local crustal dust to cryoconite. The volume-size distribution for the cryoconite particles also indicated bi-modal distribution graphs with volume median diameters ranging from 0.57 to 20 μm and from 20 to 100 μm, demonstrating the contribution of both LRT Asian dust and local dust inputs to cryoconite. Based on the particle size distribution, we calculated a mean number ratio of local dust contribution to cryoconite ranging from 0.7% (Baishui Glacier No.1) to 17.6% (Shiyi Glacier) on the Tibetan Plateau. In general, the marked difference in the Nd-Sr isotopic ratios of cryoconite compared with those of large deserts probably indicates that, materials from the western deserts have not been easily transported to the hinterland of Tibetan Plateau by the Westerlies under the current climatic conditions, and the arid deserts on the Tibetan Plateau are the most likely sources for cryoconite deposition. The resistance of the Tibetan Plateau to the Westerlies may have caused such phenomena, especially for LRT eolian dust transported over the Tibetan Plateau. Thus, this work is of great importance in understanding the large scale eolian dust transport and climate over the Tibetan Plateau.

  6. Granitoids of the Ufalei block (South Urals): Sr-Nd isotope systematics, geodynamic position and genetic reconstructions

    NASA Astrophysics Data System (ADS)

    Ronkin, Yu. L.; Shardakova, G. Yu.; Maslov, A. V.; Shagalov, E. S.; Lepikhina, O. P.

    2009-04-01

    Petrogeochemical and isotopic-geochronological signatures in granitoids developed in structures with complex geological history represent an important feature for reconstructing paleogeodynamic settings. Granitoids are widespread in the western slope of the Urals, where the Uralian Orogen contacts via a collage of different-age blocks of the east European Platform. The Ufalei block located in the Central Urals megazone at the junction between the South and Middle Urals’ segments represents one such boundary structure with multistage geological evolution. The isotopic ages obtained by different methods for acid igneous rocks range from 1290 to 245 Ma. We determined close Rb-Sr and Sm-Nd ages (317 Ma) for granites of the Nizhnii Ufalei Massif. By their petrochemical parameters, granitoids and host granite-gneisses differ principally from each other: the former are close to subduction-related, while the latter, to continental-riftogenic varieties. The primary ratio (87Sr/86Sr)0 = 0.70428 and ɛNd ≈ +4 values indicate significant contribution of oceanic (island-arc?) material to the substrate, which served as a source for granites of the Nizhnii Ufalei Massif. Model Nd ages of granites vary from 641 to 550 Ma. Distinct oceanic rocks and varieties with such ages are missing from the surrounding structures. New isotopic dates obtained for ultramafic and mafic rocks from different zones of the Urals related to the Cadomian cycle imply development of unexposed Upper Riphean-Vendian “oceanic” rocks in the central part of the Ufalei block, which played a substantial role in the formation of the Nizhnii Ufalei granitoids. Such rocks could be represented, for example, by fragments of the Precambrian Timanide-type ophiolite association. The analysis of original materials combined with published data point to the heterogeneous composition and structure of the Ufalei block and a significant part of the western segment of the Central Uralian Uplift and extremely complex

  7. Nd, Sr and O isotopic study of the petrogenesis of two syntectonic members of the New Hampshire Plutonic Series

    NASA Astrophysics Data System (ADS)

    Lathrop, A. S.; Blum, Joel D.; Chamberlain, C. Page

    1996-07-01

    Nd, Sr and O isotope systematics were used to investigate the petrogenesis of two adjacent plutons of the Bethlehem Gneiss (BG) and the Kinsman Quartz Monzonite (KQM), exposed within the Central Maine Terrane (CMT) of New England. Both are Acadian-aged (≈413 Ma) synmetamorphic and syntectonic members of the New Hampshire Plutonic Series (NHPS). Potential source rocks analyzed for this study include Silurian and Devonian metasedimentary rocks of the CMT, and Ordovician metasedimentary rocks and granitic gneisses of the Bronson Hill Anticlinorium (BHA), which border the CMT to the west. The ɛSr(413), ɛNd(413) and δ18O values for the KQM range from 56.3 to 120.0, 2.8 to -6.4, and 7.6‰ to 12.9‰, respectively; values for the BG range from 7.4 to 144.7, 0.6 to -9.3, and 8.3‰ to 11.3‰, respectively; and values for possible source rocks range from 38.1 to 654.2, -10.7 to 5.4, and 6.2‰ to 14.1‰, respectively. Both the BG and KQM have extremely heterogeneous initial isotopic compositions consistent with mixing of multiple crustal source rocks, and neither contains a volumetrically significant (i.e., ≥10%) mantlederived component. Overlapping values of ɛNd(413), ɛSr(413) and δ18O values for both the BG and KQM samples resemble values for metasedimentary host rocks of the CMT and BHA. We observe no systematic correlations between ɛNd and ɛSr values for either the BG or the KQM. The ɛSr and δ18O values for the BG do not form any simple mixing trends, nor is there any direct correlation between the isotopic compositions of contact BG samples and their adjacent host rocks, in contrast to our observations for the KQM (Lathrop et al. 1994). We propose that the KQM and BG magmas were generated through anatexis of metasedimentary rocks from both the BHA and CMT in response to crystal thickening during the Acadian orogeny. Melting may have been initiated within CMT metasediments in response to high heat production in these mid-crustal rocks combined with

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

    NASA Astrophysics Data System (ADS)

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

    2014-05-01

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

  9. Isotopic evolution of Mauna Loa volcano

    NASA Astrophysics Data System (ADS)

    Kurz, Mark D.; Kammer, David P.

    1991-04-01

    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 3He/ 4He ( ˜ 16-20 times atmospheric), higher 206Pb/ 204Pb ( ˜ 18.2), and lower 87Sr/ 86Sr ( ˜ 0.70365) ratios than the younger Kau samples (having He, Pb and Sr ratios of approximately 8.5 × atmospheric, 18.1 and 0.70390, respectively). The historical lavas are distinct in having intermediate Sr and Pb isotopic compositions with 3He/ 4He ratios similar to the other young Kau basalt ( ˜ 8.5 × 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. An asthenospheric source, or variation within the plume source, is considered more likely than

  10. Method to make accurate concentration and isotopic measurements for small gas samples

    NASA Astrophysics Data System (ADS)

    Palmer, M. R.; Wahl, E.; Cunningham, K. L.

    2013-12-01

    Carbon isotopic ratio measurements of CO2 and CH4 provide valuable insight into carbon cycle processes. However, many of these studies, like soil gas, soil flux, and water head space experiments, provide very small gas sample volumes, too small for direct measurement by current constant-flow Cavity Ring-Down (CRDS) isotopic analyzers. Previously, we addressed this issue by developing a sample introduction module which enabled the isotopic ratio measurement of 40ml samples or smaller. However, the system, called the Small Sample Isotope Module (SSIM), does dilute the sample during the delivery with inert carrier gas which causes a ~5% reduction in concentration. The isotopic ratio measurements are not affected by this small dilution, but researchers are naturally interested accurate concentration measurements. We present the accuracy and precision of a new method of using this delivery module which we call 'double injection.' Two portions of the 40ml of the sample (20ml each) are introduced to the analyzer, the first injection of which flushes out the diluting gas and the second injection is measured. The accuracy of this new method is demonstrated by comparing the concentration and isotopic ratio measurements for a gas sampled directly and that same gas measured through the SSIM. The data show that the CO2 concentration measurements were the same within instrument precision. The isotopic ratio precision (1σ) of repeated measurements was 0.16 permil for CO2 and 1.15 permil for CH4 at ambient concentrations. This new method provides a significant enhancement in the information provided by small samples.

  11. Integrated Extraction Chromatographic Separation of the Lithophile Elements Involved in Long-Lived Radiogenic Isotope Systems (Rb-Sr, U-Th-Pb, Sm-Nd, La-Ce, and Lu-Hf) Useful in Geochemical and Environmental Sciences.

    PubMed

    Pin, Christian; Gannoun, Abdelmouhcine

    2017-02-21

    A fast and efficient sample preparation method in view of isotope ratio measurements is described, allowing the separation of 11 elements involved, either as "parent" or as "daughter" isotopes, in six radiogenic isotope systems used as chronometers and tracers in earth, planetary, and environmental sciences. The protocol is based on small extraction chromatographic columns, used either alone or in tandem, through which a single nitric acid solution is passed, without any intervening evaporation step. The columns use commercially available extraction resins (Sr resin, TRU resin, Ln resin, RE resin, and again Ln resin for isolating Sr and Pb, LREE then La-Ce-Nd-Sm, Lu(Yb), and Hf, Th, and U, respectively) along with an additional, in-house prepared resin for separating Rb. A simplified scheme is proposed for samples requiring the separation of Sr, Pb, Nd, and Hf only. Adverse effects of troublesome major elements (Fe 3+ , Ti) are circumvented by masking with ascorbic acid and hydrofluoric acid, respectively. Typical recoveries in the 85-95% range are achieved, with procedural blanks of 10-100 pg, negligible with regard to the amounts of analytes processed. The fractions separated are suitable for high precision isotope ratio measurements by TIMS or MC-ICP-MS, as demonstrated by the repeat analyses of several international reference materials of basaltic composition for 87 Sr/ 86 Sr, 208,207,206 Pb/ 204 Pb, 143 Nd/ 144 Nd, 176 Hf/ 177 Hf, and 230 Th/ 232 Th. Concentration data could be obtained by spiking and equilibrating the sample with appropriate isotopic tracers before the onset of the separation process and, finally, measuring the isotope ratios modified by the isotope dilution process.

  12. Pb and Sr isotope measurements by inductively coupled plasma mass spectrometer: efficient time management for precision improvement

    NASA Astrophysics Data System (ADS)

    Monna, F.; Loizeau, J.-L.; Thomas, B. A.; Guéguen, C.; Favarger, P.-Y.

    1998-08-01

    One of the factors limiting the precision of inductively coupled plasma mass spectrometry is the counting statistics, which depend upon acquisition time and ion fluxes. In the present study, the precision of the isotopic measurements of Pb and Sr is examined. The time of measurement is optimally shared for each isotope, using a mathematical simulation, to provide the lowest theoretical analytical error. Different algorithms of mass bias correction are also taken into account and evaluated in term of improvement of overall precision. Several experiments allow a comparison of real conditions with theory. The present method significantly improves the precision, regardless of the instrument used. However, this benefit is more important for equipment which originally yields a precision close to that predicted by counting statistics. Additionally, the procedure is flexible enough to be easily adapted to other problems, such as isotopic dilution.

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

    DOE Office of Scientific and Technical Information (OSTI.GOV)

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

    2008-11-17

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

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

    NASA Technical Reports Server (NTRS)

    Wadge, G.; Wooden, J. L.

    1982-01-01

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

  15. Geochemical, isotopic (Sr-Nd-Pb) and geochronological (Ar-Ar and U-Pb) constraints on Quaternary bimodal volcanism of the Nigde Volcanic Complex (Central Anatolia, Turkey)

    NASA Astrophysics Data System (ADS)

    Aydin, F.; Siebel, W.; Uysal, I.; Ersoy, E. Y.; Schmitt, A. K.; Sönmez, M.; Duncan, R.

    2012-04-01

    The Nigde Volcanic Complex (NVC) is a major Late Neogene-Quaternary volcanic centre within the Cappadocian Volcanic Province of Central Anatolia. The Late Neogene evolution of the NVC generally initiated with the eruption of extensive andesitic-dacitic lavas and pyroclastic flow deposits, and minor basaltic lavas. This stage was followed by a Quaternary bimodal magma suite which forms Na-alkaline/transitional basaltic and high-K calc-alkaline to alkaline silicic volcanic rocks. In this study, we present new geochemical, isotopic (Sr-Nd-Pb) and geochronological (Ar-Ar and U-Pb) data for the bimodal volcanic suite within the NVC. Recent data suggest that the eruption of this suite took place ranges between ~650 and ~220 ka (Middle-Late Pleistocene). Silicic rocks consisting of rhyolite and associated pumice-rich pyroclastic fall out and surge deposits define a narrow range of 143Nd/144Nd isotope ratios (0.5126-0.5127), and show virtually no difference in Pb isotope composition (206Pb/204Pb = 18.84-18.87, 207Pb/204Pb = 15.64-15.67 and 208Pb/204Pb = 38.93-38.99). 87Sr/86Sr isotopic compositions of the silicic (0.704-0.705) and basaltic rocks (0.703-0.705) are rather similar reflecting a common source. The most mafic sample from basaltic rocks related to monogenetic cones is characterized by 87Sr/86Sr = 0.704, 143Nd/144Nd = 0.5127, 206Pb/204Pb = 18.80, 207Pb/204Pb = 15.60 and 208Pb/204Pb = 38.68. These values suggest a moderately depleted signature of the mantle source. The geochronological and geochemical data suggest that NVC silicic and basaltic rocks are genetically closely related to each other. Mantle derived differentiated basaltic melts which experienced low degree of crustal assimilation are suggested to be the parent melt of the rhyolites. Further investigations will focus on the spatial and temporal evolution of Quaternary bimodal magma suite in the NVC and the genetic relation between silicic and basaltic rocks through detailed oxygen isotope analysis and (U

  16. Strontium stable isotope behaviour accompanying basalt weathering

    NASA Astrophysics Data System (ADS)

    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.

  17. Methodological development for 87Sr/86Sr measurement in olive oil and preliminary discussion of its use for geographical traceability of PDO Nîmes (France).

    PubMed

    Medini, Salim; Janin, Myriam; Verdoux, Patrick; Techer, Isabelle

    2015-03-15

    The lack of a geographical identification protocol for olive oils can lead to fraud and health risks. As some works call for Sr isotopes for the geographical identification of agri-food products, this study focus on the feasibility of extracting Sr from olive oils for isotopic measurements by TIMS. In fact, existing protocols for purification of Sr are unsuitable for lipid matrix. The defined protocol is applied to samples of PDO Nîmes olive oil. The accuracy of the extraction procedure is tested against isotopic standards. The values obtained are in conformity with NIST certified values. This consistency demonstrates that no modification of (87)Sr/(86)Sr ratio is brought about by this protocol. Consequently, the method is preliminary used on PDO Nîmes and Moroccan oils to evaluate the feasibility of a discriminant Sr signature on the two geographical products. This study provides promising results for the geographical discrimination and identification of PDO olive oils. Copyright © 2014 Elsevier Ltd. All rights reserved.

  18. The Cenozoic seawater 87Sr/86Sr curve: Data review and implications for correlation of marine strata

    NASA Astrophysics Data System (ADS)

    Koepnick, R. B.; Denison, R. E.; Dahl, D. A.

    1988-12-01

    The strontium isotopic ratio (87Sr/86Sr) in seawater changes slowly over geologic time. This variation is caused by changes in the relative contribution of Sr from various isotopically distinct sources within the crust. The most important of these are high-ratio sialic rocks from continents and low-ratio mafic volcanic and mafic intrusive rocks from continental margins and ocean basins. A plot of Sr isotope ratio versus age for Phanerozoic marine samples produces a curve exhibiting many episodes of increasing and decreasing values. This variation can be used as a basis for temporal correlation of marine carbonate, sulfate, and phosphate sediments. Temporal correlations can be made between high-latitude and low-latitude sequences, deepwater and shallow-water sequences, and normal-marine and restricted-marine (hypersaline/hyposaline) sequences. Satisfactory biostratigraphic correlations between such sequences are often hampered by either the absence of age-diagnostic fossils or by the provinciality of faunal and floral assemblages. Rapid change that took place in the 87Sr/86Sr of seawater during most of the Cenozoic makes this era particularly well suited for precise temporal correlation. The seawater curve for the Cenozoic is subdivided into three segments: Quaternary to mid-Miocene, mid-Miocene to late Eocene, and late Eocene to early Paleocene. The mid-Miocene to late Eocene curve segment exhibits a particularly steep slope, making this a promising interval for high-resolution stratigraphic correlation. Although current data generally support the present configuration of the seawater curve, some revision of the curve is probably required in the vicinity of the Oligocene-Eocene boundary. Establishment of the general configuration of the seawater curve for the Cenozoic has promoted efforts to refine the curve on the basis of construction of detailed Sr isotope profiles within individual stratigraphic sequences. A Sr isotope profile at Deep Sea Drilling Project (DSDP

  19. Integrating isotopic fingerprinting with petrology: how do igneous rocks evolve?

    NASA Astrophysics Data System (ADS)

    Davidson, J. P.

    2002-12-01

    In the title of his seminal work, N.L. Bowen recognized the fundamental importance of magmatic evolution in producing the spectrum of igneous rocks. Indeed it is difficult to imagine a hot highly reactive fluid passing through c. 100 km of a chemically distinct medium (lithosphere) without evolving through cooling, crystallization and interaction with the wall rocks. The fact that magmas evolve - almost invariably through open system processes - has been largely marginalized in the past 30 years by the desire to use them as probes of mantle source regions. This perspective has been driven principally by advances offered by isotope geochemistry, through which components and sources can be effectively fingerprinted. Two fundamental observations urge caution in ignoring differentiation effects; 1) the scarcity of truly primary magmas according to geochemical criteria (recognized long ago by petrologists), and 2) the common occurrence of petrographic criteria attesting to open system evolution. Recent advances in multicollector mass spectrometry permit integration of the powerful diagnostic tools of isotope geochemistry with petrographic observations through accurate and precise analysis of small samples. Laser ablation and microdrilling enable sampling within and between mineral phases. The results of our microsampling investigations give widespread support for open system evolution of magmas, and provide insights into the mechanisms and timescales over which this occurs. For example; 1) core-rim decreases in 87Sr/86Sr in zoned plagioclase crystals from 1982 lavas of El Chichon volcano, Mexico, argue that the zoning and isotopic changes are in response to magma recharge mixing with an originally contaminated resident magma; 2) Single grain and intra-grain isotopic analyses of mineral phases from Ngauruhoe andesites (New Zealand) are highly variable, arguing that bulk rock data reflect mechanical aggregations of components which have evolved in discrete domains of the

  20. Elemental and Sr-Nd-Pb isotope geochemistry of the Florianópolis Dyke Swarm (Paraná Magmatic Province): crustal contamination and mantle source constraints

    NASA Astrophysics Data System (ADS)

    Marques, L. S.; De Min, A.; Rocha-Júnior, E. R. V.; Babinski, M.; Bellieni, G.; Figueiredo, A. M. G.

    2018-04-01

    The Florianópolis Dyke Swarm is located in Santa Catarina Island, comprising also the adjacent continental area, and belongs to the Paraná Magmatic Province (PMP). The dyke outcrops in the island are 0.1-70 m thick and most of them are coast-parallel (NE-SW trending), with subordinate NW-SE trending. The vast majority of the dykes has SiO2 varying from 50 to 55 wt% and relatively high-Ti (TiO2 > 3 wt%) contents and these rocks were divided using the criteria commonly used to distinguish the different magma-types identified in the volcanic rocks from the PMP. The Urubici dykes (Sr > 550 μg/g) are the most abundant and some of them experienced crustal contamination reaching to 10%, as evidenced by low P2O5/K2O (0.30-0.21), high (Rb/Ba)PM (1.0-2.2), and radiogenic Sr and Pb isotope compositions (87Sr/86Sri up to 0.70716 (back to 125 Ma) and 206Pb/204Pbm up to 19.093). The Pitanga (Sr < 550 μg/g) and the basaltic trachyandesite dykes are less abundant and almost all of them were also substantially affected by at least 15% of crustal assimilation, evidenced by high (Rb/Ba)PM (up to 2.6) and Sr (87Sr/86Sri = 0.70737-0.71758) and Pb (206Pb/204Pbm = 18.446-19.441) isotope ratios, as well as low P2O5/K2O values (0.30-0.18). The low-Ti (TiO2 < 2 wt%) dykes are scarce and show a large compositional variability (SiO2: 50.4-64.5 wt%), with similar geochemical characteristics of the low-Ti volcanic rocks (Gramado-Palmas) from southern PMP, although the most primitive dykes show hybrid characteristics of Ribeira and Esmeralda magmas. The presence of granitic xenoliths with border reactions and dykes with diffuse contacts indicate that crustal contamination probably occurred by assimilation from re-melted the host rocks. Considering only the high-Ti Urubici dykes that were not affected by crustal contamination, the Sr, Nd and Pb isotope mixing modelling indicates the participation of a heterogeneous metasomatized (refertilized) subcontinental lithospheric mantle (SCLM). This

  1. Geographical origin of Amazonian freshwater fishes fingerprinted by ⁸⁷Sr/⁸⁶Sr ratios on fish otoliths and scales.

    PubMed

    Pouilly, Marc; Point, David; Sondag, Francis; Henry, Manuel; Santos, Roberto V

    2014-08-19

    Calcified structures such as otoliths and scales grow continuously throughout the lifetime of fishes. The geochemical variations present in these biogenic structures are particularly relevant for studying fish migration and origin. In order to investigate the potential of the (87)Sr/(86)Sr ratio as a precise biogeochemical tag in Amazonian fishes, we compared this ratio between the water and fish otoliths and scales of two commercial fish species, Hoplias malabaricus and Schizodon fasciatus, from three major drainage basins of the Amazon: the Madeira, Solimões, and Tapajós rivers, displaying contrasted (87)Sr/(86)Sr ratios. A comparison of the (87)Sr/(86)Sr ratios between the otoliths and scales of the same individuals revealed similar values and were very close to the Sr isotopic composition of the local river where they were captured. This indicates, first, the absence of Sr isotopic fractionation during biological uptake and incorporation into calcified structures and, second, that scales may represent an interesting nonlethal alternative for (87)Sr/(86)Sr ratio measurements in comparison to otoliths. Considering the wide range of (87)Sr/(86)Sr variations that exist across Amazonian rivers, we used variations of (87)Sr/(86)Sr to discriminate fish origin at the basin level, as well as at the sub-basin level between the river and savannah lakes of the Beni River (Madeira basin).

  2. Temporal Variations in the Mantle Source of MORB near the Vema Fracture Zone (Central Atlantic): Nd and Sr Isotopes in Peridotites and Basaltic Glasses

    NASA Astrophysics Data System (ADS)

    Cipriani, A.; Cipriani, A.; Brunelli, D.; Brueckner, H. K.; Brueckner, H. K.; Bonatti, E.; Bonatti, E.

    2001-12-01

    Sr-Nd-Pb isotopic ratios of zero age basalts sampled along Mid-Ocean Ridges (MOR) have demonstrated that the mantle is heterogeneous at a regional scale. However, how the mantle evolves through time below a single segment of MOR it is still matter of debate. Peridotites and basaltic glasses were collected along a lithospheric section uplifted and exposed on the southern side of the Vema transform (10o North, Atlantic Ocean) along a seafloor spreading flow line for a stretch of almost 200 km (corresponding to roughly 10 my). This set of samples offers a unique opportunity to detect changes through time of the mantle signature in a segment of Mid Atlantic Ridge, by analyzing radiogenic isotopes in the clinopyroxenes (cpx) from peridotites and glasses from the overlying basalts. Work is in progress; initial Sr and Nd measurements from cpxs within peridotites indicate several things. First, the cpxs display "depleted" mantle signatures. Second, there is a considerable variation of the isotopic ratios along the exposed section (143Nd/144Nd varies from 0.51293 to 0.51345, 87Sr/86Sr varies from 0.70228 to 0.70422) and these variations occur over a short time scale (some occur within an interval of one million year). Next, the Sr and Nd ratios are inversely correlated and fall along the mantle array. Finally, cpx Nd ratios are inversely correlated with the Cr/Al ratio of the spinel and ortopyroxene (opx) from the peridotites while Sr ratios are positively correlated. Thus, the chemically most depleted peridotite with high Cr/Al ratios show the most enriched isotopic signatures, a pattern that has also been observed in alpine-type peridotites and peridotite nodules and that is generally interpreted as metasomatism by enriched fluids affecting depleted peridotite more extensively than less depleted peridotite. This may indicate that the temporal variations in the extent of melting detected by Cr/Al ratio in spinel and opx (Bonatti et al., Variations with age of mantle

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

    USGS Publications Warehouse

    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.

  4. New Isotopic Tracers for Shale Gas and Hydraulic Fracturing Fluids

    EPA Pesticide Factsheets

    The combined application of geochemistry, stable isotopes (δ18O, δ2H), strontium isotopes (87Sr/86Sr), boron isotopes (δ11B), and radium isotopes (228Ra/226Ra) provides a unique methodology for tracing and monitoring shale gas and fracking fluids in the environment.

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

    PubMed Central

    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

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

    PubMed

    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

  7. Automated Sample Preparation for Radiogenic and Non-Traditional Metal Isotopes: Removing an Analytical Barrier for High Sample Throughput

    NASA Astrophysics Data System (ADS)

    Field, M. Paul; Romaniello, Stephen; Gordon, Gwyneth W.; Anbar, Ariel D.; Herrmann, Achim; Martinez-Boti, Miguel A.; Anagnostou, Eleni; Foster, Gavin L.

    2014-05-01

    MC-ICP-MS has dramatically improved the analytical throughput for high-precision radiogenic and non-traditional isotope ratio measurements, compared to TIMS. The generation of large data sets, however, remains hampered by tedious manual drip chromatography required for sample purification. A new, automated chromatography system reduces the laboratory bottle neck and expands the utility of high-precision isotope analyses in applications where large data sets are required: geochemistry, forensic anthropology, nuclear forensics, medical research and food authentication. We have developed protocols to automate ion exchange purification for several isotopic systems (B, Ca, Fe, Cu, Zn, Sr, Cd, Pb and U) using the new prepFAST-MC™ (ESI, Nebraska, Omaha). The system is not only inert (all-flouropolymer flow paths), but is also very flexible and can easily facilitate different resins, samples, and reagent types. When programmed, precise and accurate user defined volumes and flow rates are implemented to automatically load samples, wash the column, condition the column and elute fractions. Unattended, the automated, low-pressure ion exchange chromatography system can process up to 60 samples overnight. Excellent reproducibility, reliability, recovery, with low blank and carry over for samples in a variety of different matrices, have been demonstrated to give accurate and precise isotopic ratios within analytical error for several isotopic systems (B, Ca, Fe, Cu, Zn, Sr, Cd, Pb and U). This illustrates the potential of the new prepFAST-MC™ (ESI, Nebraska, Omaha) as a powerful tool in radiogenic and non-traditional isotope research.

  8. Calcium biogeochemical cycle at the beech tree-soil solution interface from the Strengbach CZO (NE France): insights from stable Ca and radiogenic Sr isotopes

    NASA Astrophysics Data System (ADS)

    Schmitt, Anne-Désirée; Gangloff, Sophie; Labolle, François; Chabaux, François; Stille, Peter

    2017-09-01

    Calcium (Ca) is the fourth most abundant element in mineral nutrition and plays key physiological and structural roles in plant metabolism. At the soil-water-plant scale, stable Ca isotopes are a powerful tool for the identification of plant-mineral interactions and recycling via vegetation. Radiogenic Sr isotopes are often used as tracers of Ca sources and mixtures of different reservoirs. In this study, stable Ca and radiogenic Sr are combined and analysed in several organs from two beech trees that were collected in June and September in the Strengbach critical zone observatory (CZO) (NE France) and in corresponding soil solutions. At the beech-tree scale, this study confirms the field Ca adsorption (i.e., physico-chemical mechanism and not vital effects) on carboxyl acid groups of pectin in the apoplasm of small roots. The analysis of the xylem sap and corresponding organs shows that although the Strengbach CZO is nutrient-poor, Ca seems to be non-limiting for tree-growth. Different viscosities of xylem sap between the stemwood and branches or leaves can explain δ44/40Ca values in different tree-organs. The bark and phloem 40Ca-enrichments could be due to Ca-oxalate precipitation in the bark tissues and in the phloem. The results from this study regarding the combination of these two isotopic systems show that the isotopic signatures of the roots are dominated by Ca fractionation mechanisms and Sr, and thus Ca, source variations. In contrast, translocation mechanisms are only governed by Ca fractionation processes. This study showed that at the root-soil solution interface, litter degradation was not the main source of Ca and Sr and that the soil solutions are not the complement of uptake by roots for samples from the 2011/2013 period. The opposite is observed for older samples. These observations indicate the decreasing contribution of low radiogenic Sr fluxes, such as recycling, alimenting the soil solutions. Such reduced importance of nutrient uptake and

  9. Large-scale purification of 90Sr from nuclear waste materials for production of 90Y, a therapeutic medical radioisotope.

    PubMed

    Wester, Dennis W; Steele, Richard T; Rinehart, Donald E; DesChane, Jaquetta R; Carson, Katharine J; Rapko, Brian M; Tenforde, Thomas S

    2003-07-01

    A major limitation on the supply of the short-lived medical isotope 90Y (t1/2 = 64 h) is the available quantity of highly purified 90Sr generator material. A radiochemical production campaign was therefore undertaken to purify 1,500 Ci of 90Sr that had been isolated from fission waste materials. A series of alkaline precipitation steps removed all detectable traces of 137Cs, alpha emitters, and uranium and transuranic elements. Technical obstacles such as the buildup of gas pressure generated upon mixing large quantities of acid with solid 90Sr carbonate were overcome through safety features incorporated into the custom-built equipment used for 90Sr purification. Methods are described for analyzing the chemical and radiochemical purity of the final product and for accurately determining by gravimetry the quantities of 90Sr immobilized on stainless steel filters for future use.

  10. Sr, Nd and Pb Isotope Geochemistry of Near-ridge Seamounts in Eastern Pacific: Implications for Upper Mantle Composition and EPR Magmatic Segmentation

    NASA Astrophysics Data System (ADS)

    Castillo, P. R.; White, W. M.; Batiza, R.

    2005-12-01

    Near-ridge seamount lavas tend to reflect the true composition of the upper mantle source of MORB because these are generated by relatively smaller degrees of melting of smaller volumes of the mantle compared to nearby axial lavas; they also by-pass the axial chamber mixing and fractionation processes that are responsible for the relatively more uniform chemical and isotopic composition of normal-MORB. New Sr, Nd and Pb isotope data combined with published data for lavas from near-ridge seamounts on either side of the EPR segment between the 11o45' OSC and Orozco Transform at 15o00' show latitudinal isotopic variation very similar to that shown by the rise axial lavas (Castillo et al., G3 1, 1999). Seamount and axial lavas at both ends of the rise segment have on average slightly higher and more limited range of 143Nd/144Nd, but slightly lower 206Pb/204Pb and 87Sr/86Sr ratios than lavas at the center of the segment. Some of the seamounts are located on ~8 Ma rise flank crust although most of the seamount lavas are fairly young (e.g., lavas from Seamount 6 on ~3 Ma crust are only 3 to 900 kyr - Graham et al., Nature 326, 1987). Thus near-ridge seamount isotope data provide the first documentation for a large-scale (~350 km long x ~720 km wide), systematic compositional variation of the upper mantle source of EPR MORB. Such a scale of variation is larger and longer than the size and <1 myr life span of the majority of non-transform offsets, which are supposed to be responsible for the along-axis compositional variations of EPR MORB according to the "bottoms up" model of magmatic segmentation.

  11. High-Precision In Situ 87Sr/86Sr Analyses through Microsampling on Solid Samples: Applications to Earth and Life Sciences

    PubMed Central

    Di Salvo, Sara; Casalini, Martina; Marchionni, Sara; Adani, Teresa; Ulivi, Maurizio; Tommasini, Simone; Avanzinelli, Riccardo; Mazza, Paul P. A.; Francalanci, Lorella

    2018-01-01

    An analytical protocol for high-precision, in situ microscale isotopic investigations is presented here, which combines the use of a high-performing mechanical microsampling device and high-precision TIMS measurements on micro-Sr samples, allowing for excellent results both in accuracy and precision. The present paper is a detailed methodological description of the whole analytical procedure from sampling to elemental purification and Sr-isotope measurements. The method offers the potential to attain isotope data at the microscale on a wide range of solid materials with the use of minimally invasive sampling. In addition, we present three significant case studies for geological and life sciences, as examples of the various applications of microscale 87Sr/86Sr isotope ratios, concerning (i) the pre-eruptive mechanisms triggering recent eruptions at Nisyros volcano (Greece), (ii) the dynamics involved with the initial magma ascent during Eyjafjallajökull volcano's (Iceland) 2010 eruption, which are usually related to the precursory signals of the eruption, and (iii) the environmental context of a MIS 3 cave bear, Ursus spelaeus. The studied cases show the robustness of the methods, which can be also be applied in other areas, such as cultural heritage, archaeology, petrology, and forensic sciences. PMID:29850369

  12. Sediment Sources, Depositional Environment, and Diagenetic Alteration of the Marcellus Shale, Appalachian Basin, USA: Nd, Sr, Li and U Isotopic Constraints

    NASA Astrophysics Data System (ADS)

    Phan, T. T.; Capo, R. C.; Gardiner, J. B.; Stewart, B. W.

    2017-12-01

    The organic-rich Middle Devonian Marcellus Shale in the Appalachian Basin, eastern USA, is a major target of natural gas exploration. Constraints on local and regional sediment sources, depositional environments, and post-depositional processes are essential for understanding the evolution of the basin. In this study, multiple proxies, including trace metals, rare earth elements (REE), the Sm-Nd and Rb-Sr isotope systems, and U and Li isotopes were applied to bulk rocks and authigenic fractions of the Marcellus Shale and adjacent limestone/sandstone units from two locations separated by 400 km. The range of ɛNd values (-7.8 to -6.4 at 390 Ma) is consistent with a clastic sedimentary component derived from a well-mixed source of fluvial and eolian material of the Grenville orogenic belt. The Sm-Nd isotope system and bulk REE distributions appear to have been minimally affected by post-depositional processes, while the Rb-Sr isotope system shows evidence of limited post-depositional redistribution. While REE are primarily associated with silicate minerals (80-95%), REE patterns of sequentially extracted fractions reflect post-depositional alteration at the intergranular scale. Although the chemical index of alteration (CIA = 54 to 60) suggests the sediment source was not heavily weathered, Li isotope data are consistent with progressively increasing weathering of the source region during Marcellus Shale deposition. δ238U values in bulk shale and reduced phases (oxidizable fraction) are higher than those of modern seawater and upper crust. The isotopically heavy U accumulated in these authigenic phases can be explained by the precipitation of insoluble U in anoxic/euxinic bottom water. Unlike carbonate cement within the shale, the similarity between δ238U values and REE patterns of the limestone units and those of modern seawater indicates that the limestone formed under open ocean (oxic) conditions.

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

    NASA Astrophysics Data System (ADS)

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

    2013-04-01

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

  14. Uranium-Lead Zircon Ages and Sr, Nd, and Pb Isotope Geochemistry of Selected Plutonic Rocks from Western Idaho

    USGS Publications Warehouse

    Unruh, Daniel M.; Lund, Karen; Kuntz, Mel A.; Snee, Lawrence W.

    2008-01-01

    Across the Salmon River suture in western Idaho, where allochthonous Permian to Cretaceous oceanic rocks are juxtaposed against Proterozoic North American rocks, a wide variety of plutonic rocks are exposed. Available data indicate much variation in composition, source, and structural state of these plutons. The plutonic rocks were long described as the western border zone of the Cretaceous Idaho batholith but limited pre-existing age data indicate more complicated origins. Because the affinity and age of the plutonic rocks cannot be reliably determined from field relations, TIMS U-Pb dating in conjunction with Sr, Nd, and Pb isotopic studies of selected plutons across the suture in western Idaho were undertaken. The data indicate three general groups of plutons including (1) those that intruded the island arc terranes during the Triassic and Jurassic, those that intruded near the western edge of oceanic rocks along the suture in the Early Cretaceous, and the plutons of the Idaho batholith that intruded Proterozoic North American rocks in the Late Cretaceous. Plutons that intruded Proterozoic North American rocks commonly include xenocrystic zircons and in several cases, ages could not be determined. The least radiogenic Sr and most radiogenic Nd are found among the Blue Mountains superterrane island arc samples. Suture-zone plutons have isotopic characteristics that span the range between Idaho batholith and island arc samples but mostly follow island arc signatures. Plutons of the Idaho batholith have the most radiogenic initial Pb and Sr ratios and the least radiogenic Nd of the samples analyzed.

  15. Rb-Sr, K-Ar, and stable isotope evidence for the ages and sources of fluid components of gold-bearing quartz veins in the northern Sierra Nevada foothills metamorphic belt, California

    USGS Publications Warehouse

    Böhlke, John Karl; Kistler, R. W.

    1986-01-01

    Gold-bearing quartz veins occur in and near major fault zones in deformed oceanic and island-arc rocks west of the main outcrop of the Sierra Nevada composite batholith. Veins typically occupy minor reverse faults that crosscut blueschist to amphibolite-grade metamorphic rocks whose metamorphic ages range from early Paleozoic to Jurassic. Vein micas and carbonate-quartz-mica assemblages that formed by hydrothermal metasomatism of ultramafic wall rocks in the Alleghany, Grass Valley, Washington, and Mother Lode districts yield concordant K-Ar and Rb-Sr ages. The dated veins are significantly younger than prograde metamorphism, penetrative deformation, and accretion of their host rocks to the continental margin. New and previously published mineralization ages from 13 localities in the Sierra foothills range from about 140 to 110 m.y. ago, with mean and median between 120 and 115 m.y. The age relations suggest that mineralizing fluids were set in motion by deep magmatic activity related to the resumption of east-dipping subduction along the western margin of North America following the Late Jurassic Nevadan collision event.CO 2 -bearing fluids responsible for metasomatism and much of the vein mica, carbonate, albite, and quartz deposition in several northern mines were isotopically heavy (delta 18 O [asymp] 8-14ppm; delta D between about -10 and -50ppm) and do not resemble seawater, magmatic, or meteoric waters. Metasomatic and vein-filling mica, dolomite, magnesite, and quartz in altered ultramafic rocks generally formed from fluids with similar Sr and O isotope ratios at a given locality. Consistent quartz-mica delta 18 O fractionations (delta 18 O (sub Q-M) = 4.5-4.9ppm) from various localities imply uniform equilibration temperatures, probably between 300 degrees and 350 degrees C. On a local (mine) scale, fluids responsible for both carbonate alteration of mafic and ultramafic wall rocks and albitic alteration of felsic and pelitic rocks had similar Sr isotope

  16. Pb, Sr, and Nd isotopic compositions of a suite of Large Archean, igneous rocks, eastern Beartooth Mountains - Implications for crust-mantle evolution

    NASA Technical Reports Server (NTRS)

    Wooden, J. L.; Mueller, P. A.

    1988-01-01

    Compositionally diverse Late Archean rocks (2.74-2.79 Ga old) from the eastern Beartooth Mountains (Montana and Wyoming) were studied and shown to have the same initial Pb, Sr, and Nd isotopic ratios. Lead and Sr initial ratios are higher and Nd initial values lower than predicted for rocks derived from model mantle sources and strongly indicate the involvement of an older crustal reservoir in the genesis of these rocks. A model involving subduction of continental detritus and contamination of the overlying mantle is suggested.

  17. DUPAL anomaly in the Sea of Japan: Pb, Nd, and Sr isotopic variations at the eastern Eurasian continental margin

    USGS Publications Warehouse

    Tatsumoto, M.; Nakamura, Y.

    1991-01-01

    Volcanic rocks from the eastern Eurasian plate margin (southwestern Japan, the Sea of Japan, and northeastern China) show enriched (EMI) component signatures. Volcanic rocks from the Ulreung and Dog Islands in the Sea of Japan show typical DUPAL anomaly characteristics with extremely high ??208/204 Pb (up to 143) and enriched Nd and Sr isotopic compositions (??{lunate}Nd = -3 to -5, 87Sr 86Sr = ~0.705). The ??208/204 Pb values are similar to those associated with the DUPAL anomaly (up to 140) in the southern hemisphere. Because the EMI characteristics of basalts from the Sea of Japan are more extreme than those of southwestern Japan and inland China basalts, we propose that old mantle lithosphere was metasomatized early (prior to the Proterozoic) with subduction-related fluids (not present subduction system) so that it has been slightly enriched in incompatible elements and has had a high Th/U for a long time. The results of this study support the idea that the old subcontinental mantle lithosphere is the source for EMI of oceanic basalts, and that EMI does not need to be stored at the core/ mantle boundary layer for a long time. Dredged samples from seamounts and knolls from the Yamato Basin Ridge in the Sea of Japan show similar isotopic characteristics to basalts from the Mariana arc, supporting the idea that the Yamato Basin Ridge is a spreading center causing separation of the northeast Japan Arc from Eurasia. ?? 1991.

  18. Evolution of the lithospheric mantle beneath Mt. Baekdu (Changbaishan): Constraints from geochemical and Sr-Nd-Hf isotopic studies on peridotite xenoliths in trachybasalt

    NASA Astrophysics Data System (ADS)

    Park, Keunsu; Choi, Sung Hi; Cho, Moonsup; Lee, Der-Chuen

    2017-08-01

    Major and trace element compositions of minerals as well as Sr-Nd-Hf isotopic compositions of clinopyroxenes from spinel peridotite xenoliths entrained in Late Cenozoic trachybasalt from Mt. Baekdu (Changbaishan) were used to elucidate lithospheric mantle formation and evolution in the eastern North China Craton (NCC). The analyzed peridotites were mainly spinel lherzolites with rare harzburgites. They consisted of olivine (Fo89.3-91.0), enstatite (Wo1-2En88-90Fs8-11), diopside (Wo45-50En45-51Fs4-6), and spinel (Cr# = 8.8-54.7). The peridotite residues underwent up to 25% partial melting in fertile mid-ocean-ridge basalt (MORB) mantle. Plots of the Cr# in spinel against the Mg# in coexisting olivine or spinel suggested an affinity with abyssal peridotites. Comparisons of Cr# and TiO2 in spinel were also compatible with an abyssal peridotite-like composition; however, harzburgites were slightly enriched in TiO2 because of the reaction with MORB-like melt. Temperatures estimated using two-pyroxene thermometry ranged from 750 to 1010 °C, reflecting their lithospheric mantle origin. The rare earth element (REE) patterns in clinopyroxenes of the peridotites varied from light REE (LREE) depleted to spoon shaped to LREE enriched, reflecting secondary overprinting effects of metasomatic melts or fluids on the residues from primordial melting. The calculated trace element pattern of metasomatic melt equilibrated with clinopyroxene in Mt. Baekdu peridotite showed strong enrichment in large-ion lithophile elements, Th and U together with slight fractionation in heavy REEs (HREEs) and considerable depletion in Nb and Ti. The Sr-Nd-Hf isotopic compositions of clinopyroxenes separated from the peridotites varied from more depleted than present-day MORB to bulk Earth values. However, some clinopyroxene showed a decoupling between Nd and Sr isotopes, deviating from the mantle array with a high 87Sr/86Sr ratio. This sample also showed a significant Nd-Hf isotope decoupling lying

  19. Nd-Sr-Pb isotopic variations along the Gulf of Aden - Evidence for Afar mantle plume-continental lithosphere interaction

    NASA Astrophysics Data System (ADS)

    Schilling, Jean-Guy; Kingsley, Richard H.; Hanan, Barry B.; McCully, Brian L.

    1992-07-01

    The rare-earth-element concentrations and Nd, Sr, and Pb isotopic compositions of the basalts in the Gulf of Aden are described and related to asthenospheric and lithospheric interactions with a thermal toruslike plume. Specific attention is given to the spatial and temporal traits of the mantle sources, and isotopic and geochemical data are used to determine the extent to which basaltic volcanism is derived from a mantle plume, the mantle lithosphere, and upwelling of the depleted atmosphere. The impingement and dispersion of a plume head is confirmed beneath the Afar region, and the geological record shows continental stretching and rifting prior to the impingement in the outskirts of the Horn of Africa. The data suggest that the isotopic variations along the Gulf of Aden/Red Sea/Ethiopia Rift system can be explained by the interaction of a thermal toruslike plume with the depleted asthenosphere and the overlying continental mantle lithosphere.

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

    USGS Publications Warehouse

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

    2010-01-01

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

  1. Some Pb and Sr isotopic measurements on eclogites from the Roberts Victor mine, South Africa

    USGS Publications Warehouse

    Manton, W.I.; Tatsumoto, M.

    1971-01-01

    Five nodules of eclogite, one nodule of garnet peridotite and one sample of kimberlite from the Roberts Victor mine were analyzed for concentrations of U, Th, Pb, Rb and Sr and isotopic compositions of Pb and Sr. In the eclogites, U content ranges from 0.09 to 0.26 ppm, Th from 0.35 to 1.1 ppm, Pb from 0.79 to 5.5 ppm, Rb from 2.1 to 28 ppm and Sr from 133 to 346 ppm; 206Pb/204Pb ratios range from 14.8 to 18.5, 207Pb/204Pb from 14.9 to 15.7, 208Pb/204Pb from 35.2 to 38.5. The garnet peridotite contains 0.22 ppm U, 0.97 ppm Th, 1.05 ppm Pb, 6.9 ppm Rb and 108 ppm Sr and the kimberlite contains 2.5 ppm U, 30 ppm Th, 37 ppm Pb, 113 ppm Rb and 2040 ppm Sr. The lead in the eclogites has two components, a lead pyroextractable at 1100-1200?? and a non-pyroextractable residual lead. In three of the eclogites, which are to some extent altered, a proportion of the pyroextractable lead may be contaminating lead from the kimberlite, but an altered kyanite eclogite does not appear to be contaminated by this same kimberlite. The pyroextractable lead from a less altered eclogite contains a much larger proportion of 206Pb. Compositions calculated for the residual leads vary greatly. In many of the pyroextraction runs the primary eclogitic phases disappeared and the new phases plagioclase, clinopyroxene and a magnetic iron compound were formed. Why part of the lead should have been retained by these new phases is not understood. ?? 1971.

  2. The composition and distribution of the rejuvenated component across the Hawaiian plume: Hf-Nd-Sr-Pb isotope systematics of Kaula lavas and pyroxenite xenoliths

    NASA Astrophysics Data System (ADS)

    Bizimis, Michael; Salters, Vincent J. M.; Garcia, Michael O.; Norman, Marc D.

    2013-10-01

    Rejuvenated volcanism refers to the reemergence of volcanism after a hiatus of 0.5-2 Ma following the voluminous shield building stage of Hawaiian volcanoes. The composition of the rejuvenated source and its distribution relative to the center of the plume provide important constraints on the origin of rejuvenated volcanism. Near-contemporaneous lavas from the Kaula-Niihau-Kauai ridge and the North Arch volcanic field that are aligned approximately orthogonally to the plume track can constrain the lateral geochemical heterogeneity and distribution of the rejuvenated source across the volcanic chain. Nephelinites, phonolites and pyroxenite xenoliths from Kaula Island have radiogenic Hf, Nd and unradiogenic Sr isotope compositions consistent with a time-integrated depleted mantle source. The pyroxenites and nephelinites extend to the lowest 208Pb/204Pb reported in Hawaiian rocks. These data, along with new Pb isotope data from pyroxenites from the Salt Lake Crater (Oahu) redefine the composition of the depleted end-member of the Hawaiian rejuvenated source at 208Pb/204Pb=37.35±0.05, 206Pb/204Pb = 17.75±0.03, ɛNd = 9-10, ɛHf ˜16-17 and 87Sr/88Sr <0.70305. The revised isotope composition also suggests that this depleted component may contribute to LOA and KEA trend shield stage Hawaiian lavas, consistent with the rejuvenated source being part of the Hawaiian plume and not entrained upper mantle. The isotope systematics of rejuvenated magmas along the Kaula-Niihau-Kauai-North Arch transect are consistent with a larger proportion of the rejuvenated depleted component in the periphery of the plume track rather than along its axis.

  3. Geographical traceability based on 87Sr/86Sr indicator: a first approach for PDO Lambrusco wines from Modena.

    PubMed

    Durante, Caterina; Baschieri, Carlo; Bertacchini, Lucia; Cocchi, Marina; Sighinolfi, Simona; Silvestri, Michele; Marchetti, Andrea

    2013-12-01

    The main goal of this study was to evaluate (87)Sr/(86)Sr ratio in different matrices, namely soils, branches, and grape juices, of an oenological food chain in order to develop a robust analytical strategy able to link the investigated food to its territory of origin. The (87)Sr/(86)Sr has been used as traceability marker and several aspects, affected its variability, i.e. geological features of the investigated area, the bio-available fraction of elements in the soils and the up-take of the plant, have been taken into account. Optimisation of an analytical procedure for the separation of Sr from its interferences and investigation of the analytical performances in terms of precision of used methodology have been carried out as well. This work highlighted a good match between the isotopic values monitored in the bio-available fraction of soils and their respective grape juices for almost all the investigated areas. The correlation with food satisfyingly improves when isotopic relative abundance values of branches vine are considered. Copyright © 2013 Elsevier Ltd. All rights reserved.

  4. The IRHUM (Isotopic Reconstruction of Human Migration) database - bioavailable strontium isotope ratios for geochemical fingerprinting in France

    NASA Astrophysics Data System (ADS)

    Willmes, M.; McMorrow, L.; Kinsley, L.; Armstrong, R.; Aubert, M.; Eggins, S.; Falguères, C.; Maureille, B.; Moffat, I.; Grün, R.

    2013-11-01

    Strontium isotope ratios (87Sr/86Sr) are a key geochemical tracer used in a wide range of fields including archaeology, ecology, food and forensic sciences. These applications are based on the principle that the Sr isotopic ratios of natural materials reflect the sources of strontium available during their formation. A major constraint for current studies is the lack of robust reference maps to evaluate the source of strontium isotope ratios measured in the samples. Here we provide a new dataset of bioavailable Sr isotope ratios for the major geologic units of France, based on plant and soil samples (Pangaea data repository doi:10.1594/PANGAEA.819142). The IRHUM (Isotopic Reconstruction of Human Migration) database is a web platform to access, explore and map our dataset. The database provides the spatial context and metadata for each sample, allowing the user to evaluate the suitability of the sample for their specific study. In addition, it allows users to upload and share their own datasets and data products, which will enhance collaboration across the different research fields. This article describes the sampling and analytical methods used to generate the dataset and how to use and access of the dataset through the IRHUM database. Any interpretation of the isotope dataset is outside the scope of this publication.

  5. Pb-Sr-Nd-O isotopic characterization of Mesozoic rocks throughout the northern end of the Peninsular Ranges batholith: Isotopic evidence for the magmatic evolution of oceanic arc–continental margin accretion during the Late Cretaceous of southern California

    USGS Publications Warehouse

    Kistler, Ronald W.; Wooden, Joseph L.; Premo, Wayne R.; Morton, Douglas M.

    2014-01-01

    Within the duration of the U.S. Geological Survey (USGS)–based Southern California Areal Mapping Project (SCAMP), many samples from the northern Peninsular Ranges batholith were studied for their whole-rock radioisotopic systematics (rubidium-strontium [Rb-Sr], uranium-thorium-lead [U-Th-Pb], and samarium-neodymium [Sm-Nd]), as well as oxygen (O), a stable isotope. The results of three main studies are presented separately, but here we combine them (>400 analyses) to produce a very complete Pb-Sr-Nd-O isotopic profile of an arc-continent collisional zone—perhaps the most complete in the world. In addition, because many of these samples have U-Pb zircon as well as argon mineral age determinations, we have good control of the timing for Pb-Sr-Nd-O isotopic variations.The ages and isotopic variations help to delineate at least four zones across the batholith from west to east—an older western zone (126–108 Ma), a transitional zone (111–93 Ma), an eastern zone (94–91 Ma), and a much younger allochthonous thrust sheet (ca. 84 Ma), which is the upper plate of the Eastern Peninsular Ranges mylonite zone. Average initial 87Sr/86 Sr (Sri), initial 206Pb/204Pb (206 Pbi), initial 208Pb/204Pb (average 208Pbi), initial epsilon Nd (average εNdi), and δ18O signatures range from 0.704, 18.787, 38.445, +3.1, and 4.0‰–9.0‰, respectively, in the westernmost zone, to 0.7071, 19.199, 38.777, −5, and 9‰–12‰, respectively, in the easternmost zone. The older western zone is therefore the more chemically and isotopically juvenile, characterized mostly by values that are slightly displaced from a mantle array at ca. 115 Ma, and similar to some modern island-arc signatures. In contrast, the isotopic signatures in the eastern zones indicate significant amounts of crustal involvement in the magmatic plumbing of those plutons. These isotopic signatures confirm previously published results that interpreted the Peninsular Ranges batholith as a progressively

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

    NASA Astrophysics Data System (ADS)

    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.

  7. Assessing Covariation of Holocene Monsoon Intensity and Local Moisture Conditions in Eastern and Southwestern Amazon Basin Using Speleothem δ18O and 87Sr/86Sr Values

    NASA Astrophysics Data System (ADS)

    Ward, B. M.; Wong, C. I.; Novello, V. F.; Silva, L.; McGee, D.; Cheng, H.; Wang, X.; Edwards, R. L.; Cruz, F. W., Sr.; Santos, R. V.

    2017-12-01

    δ18O records from South America offer insight into past variability of the South American Monsoon System (SAMS). Potential, however, for understanding local moisture conditions is limited as precipitation δ18O is strongly influenced by regional climate dynamics. Here we create Holocene speleothem 87Sr/86Sr records at 200-yr resolution using TIMS methods in the Center for Isotope Geochemistry at Boston College to complement existing Holocene δ18O speleothem records and investigate local moisture conditions above caves located in the eastern Amazon Basin (PAR - 4°S, 55°W) and southwestern Brazil (JAR - 21°S, 56°W). Speleothem 87Sr/86Sr variability is interpreted to reflect differences in the extent of water-rock interaction due to differences in infiltration rates under wet and dry conditions. Drier conditions promote longer residence time, enhanced water-rock interaction, and greater evolution of dripwater 87Sr/86Sr values from an initial isotopic signature acquired from the soil to the signature of the cave host rock. PAR speleothem 87Sr/86Sr values range from 0.71024 to 0.71067 and are bracketed by soil (0.71710 to 0.70956) and bedrock (0.70852 to 0.70899) values. JAR speleothem 87Sr/86Sr values range from 0.71216 to 0.71539 and are greater than bedrock values (0.70825 to 0.71219), although some speleothem values exceed the single analysis conducted of the soil isotopic composition (0.71473). JAR speleothem 87Sr/86Sr values increase from the early to mid Holocene, consistent with increase in local moisture availability associated with intensification of the SAMS suggested by decreasing δ18O values in many records from the region. Speleothem 87Sr/86Sr values at JAR decrease from the mid to late Holocene, consistent with an increase in δ18O values at PAR that suggest a decline in monsoon intensity. 87Sr/86Sr variability at JAR, however, is positively correlated with the δ18O record. Preliminary 87Sr/86Sr results from PAR are only broadly consistent with

  8. Reconstruction of the Eocene Arctic Ocean Using Ichthyolith Isotope Analyses

    NASA Astrophysics Data System (ADS)

    Gleason, J. D.; Thomas, D. J.; Moore, T. C.; Waddell, L. M.; Blum, J. D.; Haley, B. A.

    2007-12-01

    Nd, Sr, O and C isotopic compositions of Eocene fish debris (teeth, bones, scales), and their reduced organic coatings, have been used to reconstruct water mass composition, water column structure, surface productivity and salinities of the Arctic Ocean Basin at Lomonosov Ridge between 55 and 44 Ma. Cleaned ichthyolith samples from IODP Expedition 302 (ACEX) record epsilon Nd values that range from -5.7 to -7.8, distinct from modern Arctic Intermediate Water (-10.5) and North Atlantic Deep Water. These Nd values may record some exchange with Pacific/Tethyan water masses, but inputs from local continental sources are more likely. Sr isotopic values are consistent with a brackish-to-fresh water surface layer (87Sr/86Sr = 0.7079-0.7087) that was poorly mixed with Eocene global seawater (0.7077-0.7078). Leaching experiments show reduced organic coatings to be more radiogenic (>0.7090) than cleaned ichthyolith phosphate. Ichthyolith Sr isotopic variations likely reflect changes in localized river input as a function of shifts in the Arctic hydrologic cycle, and 87Sr/86Sr values might be used as a proxy for surface water salinity. Model mixing calculations indicate salinities of 5 to 20 per mil, lower than estimates based on O isotopes from fish bone carbonate (16 to 26 per mil). Significant salinity drops (i.e., 55 Ma PETM and 48.5 Ma Azolla event) registered in oxygen isotopes do not show large excursions in the 87Sr/86Sr data. Carbon isotopes in fish debris record a spike in organic activity at 48.5 Ma (Azolla event), and otherwise high-productivity waters between 55 and 44 Ma. The combined Sr-Nd-O-C isotopic record is consistent with highly restricted basin-wide circulation in the Eocene, indicative of a highly stratified water column with anoxic bottom waters, a "fresh" water upper layer, and enhanced continental runoff during warm intervals until the first appearance of ice rafted debris at 45 Ma.

  9. The Chronology and Petrogenesis of the Mare Basalt Clast from Lunar Meteorite Dhofar 287: Rb-Sr and Sm- Nd Isotopic Studies

    NASA Technical Reports Server (NTRS)

    Shih, C.-Y.; Nyquist, L. E.; Reese, Y.; Wiesmann, H.; Nazarov, M. A.; Taylor, L. A.

    2002-01-01

    The Sm-Nd isochron for lunar mare basalt meteorite Dhofar 287A yields T = 3.46 +/- 0.03 Ga and Nd = 0.6 +/- 0.3. Its Rb-Sr isotopic system is severely altered. The basalt is unique, probably coming from an enriched mantle source. Additional information is contained in the original extended abstract.

  10. Age, geochemical and Sr Nd Pb isotopic constraints for mantle source characteristics and petrogenesis of Teru Volcanics, Northern Kohistan Terrane, Pakistan

    NASA Astrophysics Data System (ADS)

    Khan, S. D.; Stern, R. J.; Manton, M. I.; Copeland, P.; Kimura, J. I.; Khan, M. A.

    2004-11-01

    This paper presents new geochemical and geochronology data for the Teru Volcanic Formation (previously known as the Shamran Volcanics) exposed west of Gilgit in the Kohistan terrane of the Pakistani Himalayas. The Teru Volcanic Formation ranges from basalt through andesite to rhyolite and has subalkaline and midalkaline affinities. Trace-element compositions and isotopic characteristics suggest these magmas were formed in a subduction zone setting; isotopic studies also support this conclusion. It is suggested that these lavas originated from a depleted mantle source, which experienced contamination by variable subduction components. Model mixing calculations using 87Sr/ 86Sr and 143Nd/ 144Nd data suggest that addition of 0.2-0.6% of Indus margin sediments and/or 2-4% of fluids derived from Indus margin sediment can generate the compositional variation of the Teru Volcanic Formation. Two samples from the Teru Volcanic Formation yielded 40Ar/ 39Ar ages of 43.8+0.5 and 32.5+0.4 Ma. These ages make the volcanic rocks of the Teru Volcanic Formation the youngest reported in the Kohistan terrane. These volcanic rocks unconformably overly the Shunji Pluton, which has a 65 Ma Rb-Sr whole-rock isochron age. The results of this research suggest that subduction-related volcanism was active until 33 Ma in the India-Asia collision zone.

  11. In-situ trace element and Sr isotopic compositions of mantle xenoliths constrain two-stage metasomatism beneath the northern North China Craton

    NASA Astrophysics Data System (ADS)

    Wu, Dan; Liu, Yongsheng; Chen, Chunfei; Xu, Rong; Ducea, Mihai N.; Hu, Zhaochu; Zong, Keqing

    2017-09-01

    Subduction and collision are the key processes triggering geochemical refertilization of the lithospheric mantle beneath cratons. However, the way that the subducted plate influences the cratonic lithospheric mantle remains unclear. Here, in-situ major and trace-element and Sr isotopic compositions of peridotite and pyroxenite xenoliths carried by the Dongbahao Cenozoic basalts, located close to the northern margin of North China Craton (NCC), were examined to investigate the effects of the subducted Paleo-Asian oceanic plate on the lithospheric mantle of the NCC. Based on petrographic and geochemical features, peridotites were subdivided into two types recording two-stage metasomatism. Clinopyroxene (Cpx) in both types of peridotites show chemical zoning. In those peridotites we refer to as Type 1 peridotites, Cpx exhibit uniform convex-upward rare earth element (REE) patterns but core-rim variations in 87Sr/86Sr ratios (0.7065-0.7082 in the cores and 0.7043-0.7059 in the spongy rims), and have high (La/Yb)N ratios (> 1.12) (N means normalized to chondrite), relatively low Ti/Eu ratios (< 3756) and negative high field strength element (HFSE) (Nb, Ta, Zr, Hf and Ti) anomalies in the cores, indicating early-stage metasomatism by carbonatitic melts derived from the subducted sedimentary carbonate rocks. Cpx in the Type 2 peridotites have highly variable REE patterns (from light rare earth element (LREE)-depleted to LREE-enriched) and feature zoned Sr isotopic compositions contrasting to those in Type 1, i.e., increasing 87Sr/86Sr ratios from the cores (0.7020-0.7031) to the spongy rims (0.7035-0.7041). Accompanying variations of 87Sr/86Sr ratios, Cpx in both types of peridotites display increasing Nb/La ratios from the cores to the spongy rims. In addition, Cpx in the Type 2 peridotites show remarkably increased (La/Yb)N, Ca/Al, Sm/Hf and Zr/Hf ratios but decreased Ti/Eu and Ti/Nb ratios from the cores to the spongy rims. These features imply a later

  12. Nonmonotonic variation of seawater [sup 87]Sr/[sup 86]Sr across the Ivorian/Chadian boundary (Mississippian, Osagean): Evidence from marine cements within the Irish Waulsortian Limestone

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Douthit, T.L.; Meyers, W.J.; Hanson, G.N.

    1993-05-01

    Detailed analysis of compositionally unaltered marine fibrous cements (MFC) from a single core through the Mississippian irish Waulsortian Limestone indicates that the variation of seawater [sup 87]Sr/[sup 86]Sr is nonmonotonic across the Ivorian-Chadian boundary. This nonmonotonic variation has not been recognized by previous studies. Furthermore, marine cement yielded [sup 87]Sr/[sup 86]Sr ratios lower than previously reported values for the Ivorian-Chadian (sagean). Marine fibrous cements are interpreted to be compositionally unaltered on the basis of nonluminescent character and stable isotope (C, O) composition comparable to previous estimates of Mississippian marine calcite. The isotope chemistry (C, O, Sr) and cathodoluminescent character ofmore » the marine fibrous cements therefore remained intact during their conversion from high-Mg calcite to low-Mg calcite + microdolomite, a conversion that probably took place in marine water during precipitation of Zone 1 calcite cement, the oldest non-MFC cement. High stratigraphic resolution was obtained by restricting the sample set to a single core, 429 m long, thereby eliminating chronostratigraphic correlation errors. The core is estimated to represent about 9.8 million years of Waulsortian Limestone deposition. The maximum rate of change in seawater [sup 87]Sr/[sup 86]Sr is [minus]0.00012/Ma, comparable in magnitude to Tertiary values. The authors data document the presence of fine-scale seawater [sup 87]Sr/[sup 86]Sr modulations for the Ivorian/Chadian, in contrast to the previously published monotonic seawater [sup 87]Sr/[sup 86]Sr curve for this interval, and emphasize the importance of well characterized intraformational isotopic baselines.« less

  13. Rapid sequential determination of Pu, 90Sr and 241Am nuclides in environmental samples using an anion exchange and Sr-Spec resins.

    PubMed

    Lee, M H; Ahn, H J; Park, J H; Park, Y J; Song, K

    2011-02-01

    This paper presents a quantitative and rapid method of sequential separation of Pu, (90)Sr and (241)Am nuclides in environmental soil samples with an anion exchange resin and Sr Spec resin. After the sample solution was passed through an anion exchange column connected to a Sr Spec column, Pu isotopes were purified from the anion exchange column. Strontium-90 was separated from other interfering elements by the Sr Spec column. Americium-241 was purified from lanthanides by the anion exchange resin after oxalate co-precipitation. Measurement of Pu and Am isotopes was carried out using an α-spectrometer. Strontium-90 was measured by a low-level liquid scintillation counter. The radiochemical procedure of Pu, (90)Sr and (241)Am nuclides investigated in this study validated by application to IAEA reference materials and environmental soil samples. Copyright © 2010 Elsevier Ltd. All rights reserved.

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

    NASA Astrophysics Data System (ADS)

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

    2016-07-01

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

  15. Investigation of mass dependence effects for the accurate determination of molybdenum isotope amount ratios by MC-ICP-MS using synthetic isotope mixtures.

    PubMed

    Malinovsky, Dmitry; Dunn, Philip J H; Petrov, Panayot; Goenaga-Infante, Heidi

    2015-01-01

    Methodology for absolute Mo isotope amount ratio measurements by multicollector inductively coupled plasma-mass spectrometry (MC-ICP-MS) using calibration with synthetic isotope mixtures (SIMs) is presented. For the first time, synthetic isotope mixtures prepared from seven commercially available isotopically enriched molybdenum metal powders ((92)Mo, (94)Mo, (95)Mo, (96)Mo, (97)Mo, (98)Mo, and (100)Mo) are used to investigate whether instrumental mass discrimination of Mo isotopes in MC-ICP-MS is consistent with mass-dependent isotope distribution. The parent materials were dissolved and mixed as solutions to obtain mixtures with accurately known isotope amount ratios. The level of elemental impurities in the isotopically enriched molybdenum metal powders was quantified by ICP-MS by using both high-resolution and reaction cell instruments to completely resolve spectral interferences. The Mo isotope amount ratio values with expanded uncertainty (k = 2), determined by MC-ICP-MS for a high-purity Mo rod from Johnson Matthey, were as follows: (92)Mo/(95)Mo = 0.9235(9), (94)Mo/(95)Mo = 0.5785(8), (96)Mo/(95)Mo = 1.0503(9), (97)Mo/(95)Mo = 0.6033(6), (98)Mo/(95)Mo = 1.5291(20), and (100)Mo/(95)Mo = 0.6130(7). A full uncertainty budget for the measurements is presented which shows that the largest contribution to the uncertainty budget comes from correction for elemental impurities (∼51%), followed by the contribution from weighing operations (∼26 %). The atomic weight of molybdenum was calculated to be 95.947(2); the uncertainty in parentheses is expanded uncertainty with the coverage factor of 2. A particular advantage of the developed method is that calibration factors for all six Mo isotope amount ratios, involving the (95)Mo isotope, were experimentally determined. This allows avoiding any assumption on mass-dependent isotope fractions in MC-ICP-MS, inherent to the method of double spike previously used for Mo isotope amount ratio

  16. Trace-element and Sr, Nd, Pb, and O isotopic composition of Pliocene and Quaternary alkali basalts of the Patagonian Plateau lavas of southernmost South America

    USGS Publications Warehouse

    Stern, C.R.; Frey, F.A.; Futa, K.; Zartman, R.E.; Peng, Z.; Kurtis, Kyser T.

    1990-01-01

    The Pliocene and Quaternary Patagonian alkali basalts of southernmost South America can be divided into two groups. The "cratonic" basalts erupted in areas of Cenozoic plateau volcanism and continental sedimentation and show considerable variation in 87Sr/86Sr (0.70316 to 0.70512), 143Nd/144Nd (e{open}Nd) and 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios (18.26 to 19.38, 15.53 to 15.68, and 38.30 to 39.23, respectively). These isotopic values are within the range of oceanic island basalts, as are the Ba/La, Ba/Nb, La/Nb, K/Rb, and Cs/Rb ratios of the "cratonic" basalts. In contrast, the "transitional" basalts, erupted along the western edge of the outcrop belt of the Pliocene and Quaternary plateau lavas in areas that were the locus of earlier Cenozoic Andean orogenic arc colcanism, have a much more restricted range of isotopic composition which can be approximated by 87Sr/86Sr=0.7039??0.0004, e{open}Nd, 206Pb/204Pb=18.60??0.08, 207Pb/204Pb=15.60??0.01, and 208Pb/204Pb=38.50??0.10. These isotopic values are similar to those of Andean orogenic are basalts and, compared to the "cratonic" basalts, are displaced to higher 87Sr/86Sr at a given 143Nd/144Nd and to higher 207Pb/204Pb at a given 208Pb/204Pb. The "transitional" basalts also have Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios higher than the "cratonic" and oceanic island basalts, although not as high as Andean orogenic are basalts. In contrast to the radiogenic isotopes, ??18O values for both groups of the Patagonian alkali basalts are indistinguishable and are more restricted than the range reported for Andean orogenic are basalts. Whole rock ??18O values calculated from mineral separates for both groups range from 5.3 to 6.5, while measured whole rock ??18O values range from 5.1 to 7.8. The trace element and isotopic data suggest that decreasing degrees of partial melting in association with lessened significance of subducted slabderived components are fundamental factors in the west to east transition from arc

  17. Mapping the origins of Imperial Roman workers (1st-4th century CE) at Vagnari, Southern Italy, using 87 Sr/86 Sr and δ18 O variability.

    PubMed

    Emery, Matthew V; Stark, Robert J; Murchie, Tyler J; Elford, Spencer; Schwarcz, Henry P; Prowse, Tracy L

    2018-04-18

    We obtained the oxygen and strontium isotope composition of teeth from Roman period (1st to 4th century CE) inhabitants buried in the Vagnari cemetery (Southern Italy), and present the first strontium isotope variation map of the Italian peninsula using previously published data sets and new strontium data. We test the hypothesis that the Vagnari population was predominantly composed of local individuals, instead of migrants originating from abroad. We analyzed the oxygen ( 18 O/ 16 O) and strontium ( 87 Sr/ 86 Sr) isotope composition of 43 teeth. We also report the 87 Sr/ 86 Sr composition of an additional 13 molars, 87 Sr/ 86 Sr values from fauna (n = 10), and soil (n = 5) samples local to the area around Vagnari. The 87 Sr/ 86 Sr variation map of Italy uses 87 Sr/ 86 Sr values obtained from previously published data sources from across Italy (n = 199). Converted tooth carbonate (δ 18 O DW ) and 87 Sr/ 86 Sr data indicate that the majority of individuals buried at Vagnari were local to the region. ArcGIS bounded Inverse Distance Weighting (IDW) interpolation of the pan-Italian 87 Sr/ 86 Sr data set approximates the expected 87 Sr/ 86 Sr range of Italy's geological substratum, producing the first strontium map of the Italian peninsula. Results suggest that only 7% of individuals buried at Vagnari were born elsewhere and migrated to Vagnari, while the remaining individuals were either local to Vagnari (58%), or from the southern Italian peninsula (34%). Our results are consistent with the suggestion that Roman Imperial lower-class populations in southern Italy sustained their numbers through local reproduction measures, and not through large-scale immigration from outside the Italian peninsula. © 2018 Wiley Periodicals, Inc.

  18. Applicability of 87Sr/86Sr in examining return flow of irrigation water in highly agricultural watersheds in Japan

    NASA Astrophysics Data System (ADS)

    Yoshida, T.; Nakano, T.; Shin, K. C.; Tsuchihara, T.; Miyazu, S.; Kubota, T.

    2017-12-01

    Water flows in watersheds containing extensive areas of irrigated paddies are complex because of the substantial volumes involved and the repeated cycles of water diversion from, and return to, streams. For better management of low-flow conditions, numerous studies have attempted to quantify the return flow using the stable isotopes of water; however, the temporal variation in these isotopic compositions due to fractionation during evaporation from water surfaces hinders their application to watersheds with extensive irrigated paddies. In this study, we tested the applicability of the strontium isotopes (87Sr/86Sr, hereafter Sr ratio) for studying hydrological processes in a typical agricultural watershed located on the alluvial fan of the Kinu River, namely the Gogyo River, in central Japan. The Sr ratio of water changes only because of interactions with the porous media it flows through, or because of mixing with water that has different Sr ratios. We sampled water both at a single rice paddy, and on the watershed scale in the irrigated and non-irrigated periods. The soil water under the paddy decreased as sampling depth increased, and the soil water at a depth of 1.5 m showed a similar Sr ratio to the spring. The water sampled in the drainage channel with a concrete lined bottom showed a similar Sr ratio to the irrigation water, whereas that with a soil bottom was plotted between the plots of the irrigation water and shallow aquifer. These results suggest the Sr ratio decreases as it mixes with the soil water through percolation; whereas the Sr ratio will be less likely to change when water drains from paddies via surface pathways. The streamflow samples were plotted linearly on the Sr ratio and 1/Sr plot, indicating that the streamflow was composed of two end-members; the irrigation water and the shallow aquifer. The continuous decline in the Sr ratio along the stream suggests an exfiltration of water from the shallow aquifers. The stream water during the non

  19. Oxygen isotope effect in disordered underdoped and overdoped La 2-xSr xCu 1-yZn yO 4 superconductors

    NASA Astrophysics Data System (ADS)

    Naqib, S. H.; Islam, R. S.

    2011-04-01

    The effect of oxygen isotopic substitution on the superconducting transition temperature has been studied for heavily underdoped and overdoped La 2-xSr xCu 1-yZn yO 4 compounds with different Zn contents in the CuO 2 plane. The effect of Zn on the isotope coefficient, α, was significantly more pronounced in the case of the underdoped ( x = 0.09) compounds compared to the overdoped ( x = 0.22) ones. The variation of α with disorder content can be described quite well within a model based solely on Cooper pair-breaking in the case of the underdoped compounds. This model fails to describe the behavior of α( y) for the overdoped samples, even though Zn still suppresses T c very effectively at this hole (Sr) content, indicating that the Zn induced pair-breaking is still very much at play. We discuss the implications of these findings in details by considering the Zn induced magnetism, stripe correlations, and possible changes in the superconducting order parameter as hole content in the CuO 2 plane, p (≡ x), is varied.

  20. Evidence for mass-dependent isotopic fractionation of strontium in a glaciated granitic watershed

    NASA Astrophysics Data System (ADS)

    de Souza, Gregory F.; Reynolds, Ben C.; Kiczka, Mirjam; Bourdon, Bernard

    2010-05-01

    The stable isotope composition of strontium (expressed as δ 88/86Sr) may provide important constraints on the global exogenic strontium cycle. Here, we present δ 88/86Sr values and 87Sr/ 86Sr ratios for granitoid rocks, a 150 yr soil chronosequence formed from these rocks, surface waters and plants in a small glaciated watershed in the central Swiss Alps. Incipient chemical weathering in this young system, whether of inorganic or biological origin, has no resolvable effect on the 87Sr/ 86Sr ratios and δ 88/86Sr values of bulk soils, which remain indistinguishable from bedrock in terms of Sr isotopic composition. Although due in part to the chemical heterogeneity of the forefield, the lack of a resolvable difference between soil and bedrock isotopic composition indicates that these soils have thus far witnessed minimal net loss of Sr; a low degree of chemical weathering is also implied by bulk soil chemistry. The isotopic composition of Sr in streamwater is more radiogenic than median soil, reflecting the preferential weathering of biotite in the catchment; streamwater δ 88/86Sr values, however, are indistinguishable from bulk soil δ 88/86Sr values, implying that no resolvable fractionation of Sr isotopes takes place during release to the weathering flux in the Damma forefield. Analyses of plant tissue reveal that plants ( Rhododendron and Vaccinium) preferentially assimilate the lighter isotopes of Sr such that their δ 88/86Sr values are significantly lower than those of the soils in which they grow. Additionally, δ 88/86Sr values of foliar and floral tissues are lower than those of roots, contrary to observations for Ca, for which Sr is often used as an analogue in weathering studies. We suggest that processes that discriminate against Sr in favour of Ca, due to the different nutritional requirement of plants for these two elements, are responsible for the observed contrast.

  1. The IRHUM (Isotopic Reconstruction of Human Migration) database - bioavailable strontium isotope ratios for geochemical fingerprinting in France

    NASA Astrophysics Data System (ADS)

    Willmes, M.; McMorrow, L.; Kinsley, L.; Armstrong, R.; Aubert, M.; Eggins, S.; Falguères, C.; Maureille, B.; Moffat, I.; Grün, R.

    2014-03-01

    Strontium isotope ratios (87Sr / 86Sr) are a key geochemical tracer used in a wide range of fields including archaeology, ecology, food and forensic sciences. These applications are based on the principle that the Sr isotopic ratios of natural materials reflect the sources of strontium available during their formation. A major constraint for current studies is the lack of robust reference maps to evaluate the source of strontium isotope ratios measured in the samples. Here we provide a new data set of bioavailable Sr isotope ratios for the major geologic units of France, based on plant and soil samples (Pangaea data repository doi:10.1594/PANGAEA.819142). The IRHUM (Isotopic Reconstruction of Human Migration) database is a web platform to access, explore and map our data set. The database provides the spatial context and metadata for each sample, allowing the user to evaluate the suitability of the sample for their specific study. In addition, it allows users to upload and share their own data sets and data products, which will enhance collaboration across the different research fields. This article describes the sampling and analytical methods used to generate the data set and how to use and access the data set through the IRHUM database. Any interpretation of the isotope data set is outside the scope of this publication.

  2. Grain-scale Sr isotope heterogeneity in amphibolite (retrograded UHP eclogite, Dabie terrane): Implications for the origin and flow behavior of retrograde fluids during slab exhumation

    NASA Astrophysics Data System (ADS)

    Guo, Shun; Yang, Yueheng; Chen, Yi; Su, Bin; Gao, Yijie; Zhang, Lingmin; Liu, Jingbo; Mao, Qian

    2016-12-01

    To constrain the origin and flow behavior of amphibolite-facies retrograde fluids during slab exhumation, we investigate the textures, trace element contents, and in situ strontium (Sr) isotopic compositions (using LA-MC-ICP-MS) of multiple types of epidote and apatite in the UHP eclogite and amphibolites from the Hualiangting area (Dabie terrane, China). The UHP epidote porphyroblasts in the eclogite (Ep-E), which formed at 28-30 kbar and 660-720 °C, contain high amounts of Sr, Pb, Th, Ba, and light rare earth elements (LREEs) and have a narrow range of initial 87Sr/86Sr ratios (0.70431 ± 0.00012 to 0.70454 ± 0.00010). Two types of amphibolite-facies epidote were recognized in the amphibolites. The first type of epidote (Ep-AI) developed in all the amphibolites and has slightly lower trace element contents than Ep-E. The Ep-AI has a same initial 87Sr/86Sr ratio range as the Ep-E and represents the primary amphibolite-facies retrograde product that is associated with an internally buffered fluid at 8.0-10.3 kbar and 646-674 °C. The other type of epidote (Ep-AII) occurs as irregular fragments, veins/veinlets, or reaction rims on the Ep-AI in certain amphibolites. Elemental X-ray maps reveal the presence of Ep-AI relics in the Ep-AII domains (appearing as a patchy texture), which indicates that Ep-AII most likely formed by the partial replacement of the Ep-AI in the presence of an infiltrating fluid. The distinctly lower trace element contents of Ep-AII are ascribed to element scavenging by a mechanism of dissolution-transport-precipitation during replacement. The Ep-AII in an individual amphibolite exhibits large intra- and inter-grain variations in the initial 87Sr/86Sr ratios (0.70493 ± 0.00030 to 0.70907 ± 0.00022), which are between those of the Ep-AI and granitic gneisses (wall rock of the amphibolites, 0.7097-0.7108). These results verify that the infiltrating fluid was externally derived from granitic gneisses. The matrix apatite in the amphibolites has

  3. Geochemical and NdSr isotopic composition of deep-sea turbidites: Crustal evolution and plate tectonic associations

    NASA Astrophysics Data System (ADS)

    McLennan, S. M.; Taylor, S. R.; McCulloch, M. T.; Maynard, J. B.

    1990-07-01

    Petrographic, geochemical, and isotopic data for turbidites from a variety of tectonic settings exhibit considerable variability that is related to tectonic association. Passive margin turbidites (Trailing Edge, Continental Collision) display high framework quartz (Q) content in sands, evolved major element compositions (high Si/Al, K/Na), incompatible element enrichments (high Th/Sc, La/Sc, La/Yb), negative Eu-anomalies and variable Th/U ratios. They have low 143Nd /144Nd and high 87Sr /86Sr ( ɛNd = -26 to -10; 87Sr /86Sr = 0.709 to 0.734 ), indicating a dominance of old upper crustal sources. Active margin settings (Fore Arc, Continental Arc, Back Arc, Strike Slip) commonly exhibit quite different compositions. Th/Sc varies from <0.01 to 1.8, and ɛNd varies from -13.8 to +8.3. Eu-anomalies range from no anomaly ( Eu/Eu ∗ = 1.0 ) to Eu-depletions typical of post-Archean shales ( Eu/Eu ∗ = 0.65 ). Active margin data are explained by mixtures of young arc-derived material, with variable composition and old upper crustal sources. Major element data indicate that passive margin turbidites have experienced more severe weathering histories than those from active settings. Most trace elements are enriched in muds relative to associated sands because of dilution effects from quartz and calcite and concentration of trace elements in clays. Exceptions include Zr, Hf (heavy mineral influence) and Tl (enriched in feldspar) which display enrichments in sands. Active margin sands commonly exhibit higher Eu/Eu ∗ than associated muds, resulting from concentration of plagioclase during sorting. Some associated sands and muds, especially from active settings, have systematic differences in Th/Sc ratios and Nd-isotopic composition, indicating that various provenance components may separate into different grain-size fractions during sedimentary sorting processes. Trace element abundances of modern turbidites, from both active and passive settings, differ from Archean

  4. Magnesium stable isotope ecology using mammal tooth enamel

    NASA Astrophysics Data System (ADS)

    Martin, Jeremy E.; Vance, Derek; Balter, Vincent

    2015-01-01

    Geochemical inferences on ancient diet using bone and enamel apatite rely mainly on carbon isotope ratios (δ13C) and to a lesser extent on strontium/calcium (Sr/Ca) and barium/calcium (Ba/Ca) elemental ratios. Recent developments in nontraditional stable isotopes provide an unprecedented opportunity to use additional paleodietary proxies to disentangle complex diets such as omnivory. Of particular relevance for paleodietary reconstruction are metals present in large quantity in bone and enamel apatite, providing that biologically mediated fractionation processes are constrained. Calcium isotope ratios (δ44Ca) meet these criteria but exhibit complex ecological patterning. Stable magnesium isotope ratios (δ26Mg) also meet these criteria but a comprehensive understanding of its variability awaits new isotopic data. Here, 11 extant mammal species of known ecology from a single locality in equatorial Africa were sampled for tooth enamel and, together with vegetation and feces, analyzed for δ26Mg, δ13C, Sr/Ca, and Ba/Ca ratios. The results demonstrate that δ26Mg incorporated in tooth enamel becomes heavier from strict herbivores to omnivores/faunivores. Using data from experimentally raised sheep, we suggest that this 26Mg enrichment up the trophic chain is due to a 26Mg enrichment in muscle relative to bone. Notably, it is possible to distinguish omnivores from herbivores, using δ26Mg coupled to Ba/Ca ratios. The potential effects of metabolic and dietary changes on the enamel δ26Mg composition remain to be explored but, in the future, multiproxy approaches would permit a substantial refinement of dietary behaviors or enable accurate trophic reconstruction despite specimen-limited sampling, as is often the case for fossil assemblages.

  5. Rb-Sr and Sm-Nd Studies of Olivine-Phyric Shergottites RBT 04262 and LAR 06319: Isotopic Evidence for Relationship to Enriched Basaltic Shergottites

    NASA Technical Reports Server (NTRS)

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

    2009-01-01

    RBT 04262 and LAR 06319 are two Martian meteorites recently discovered in Antarctica. Both contain abundant olivines, and were classified as olivine-phyric shergottites. A detailed petrographic study of RBT 04262 suggested it should be reclassified as a lherzolitic shergottite. However, the moderately LREE-depleted REE distribution pattern indicated that it is closely related to enriched basaltic shergottites like Shergotty, Zagami, Los Angeles, etc. In earlier studies of a similarly olivinephyric shergottite NWA 1068 which contains 21% modal olivine, it was shown that it probably was produced from an enriched basaltic shergottite magma by olivine accumulation . As for LAR 06319, recent petrographic studies suggested that it is different from either lherzolitic shergottites or the highly LREE-depleted olivine-phyric shergottites. We performed Rb-Sr and Sm-Nd isotopic analyses on RBT 04262 and LAR 06319 to determine their crystallization ages and Sr and Nd isotopic signatures, and to better understand the petrogenetic relationships between them and other basaltic, lherzolitic and depleted olivine-phyric shergottites.

  6. Acigöl rhyolite field, central Anatolia (part II): geochemical and isotopic (Sr-Nd-Pb, δ18O) constraints on volcanism involving two high-silica rhyolite suites

    NASA Astrophysics Data System (ADS)

    Siebel, W.; Schmitt, A. K.; Kiemele, E.; Danišík, M.; Aydin, F.

    2011-12-01

    The Acigöl rhyolite field erupted the most recent high-silica rhyolites within the Cappadocian Volcanic Province of central Anatolia, Turkey. It comprises two sequences of domes and pyroclastic rocks with eruption ages of ~150-200 ka (eastern group) and ~20-25 ka (western group). Compositionally, the eastern rhyolite group lavas are less evolved (SiO2 = 74-76 wt%), whereas the western group has higher silica abundance (SiO2 = ~77 wt%) with extremely depleted feldspar-compatible trace elements. Within each group, compositional variability is small and 143Nd/144Nd (0.51257-0.51265) and Pb isotope compositions (206Pb/204Pb = 18.87-18.88, 207Pb/204Pb = 15.65-15.67 and 208Pb/204Pb = 38.94-38.98) are homogeneous. The western group rhyolites have δ18O(zircon) overlapping mantle values (5.7 ± 0.2‰), whereas eastern group rhyolites are enriched in δ18O by ~0.5‰, consistent with a tendency to lower ɛNd values. By contrast, western group rhyolites have markedly more radiogenic 87Sr/86Sr ratios (0.7065-0.7091) compared to those of the eastern group (0.7059-0.7065). The presence of angular granitic xenoliths and a correlation between hydration (based on loss on ignition data) and 87Sr/86Sr in the western lavas, however, indicates that Sr was added during the eruption or post-eruption alteration. Isotope constraints preclude the possibility that the rhyolite magmas formed by partial melting of any known regional crystalline basement rocks. Basalts and andesites erupted in the periphery of the Acigöl field are characterised by 87Sr/86Sr ratios between 0.7040 and 0.7053, 143Nd/144Nd = 0.51259-0.51300, 206Pb/204Pb = 18.85-18.87, 207Pb/204Pb = 15.646-15.655, 208Pb/204Pb = 38.90-38.97. The isotopic and trace element data favour an origin of the rhyolites by mixing of basaltic/andesitic magmas with minor amounts of crustal melts and followed by extensive fractional crystallization.

  7. Hafnium isotope results from mid-ocean ridges and Kerguelen.

    USGS Publications Warehouse

    Patchett, P.J.

    1983-01-01

    176Hf/177Hf ratios are presented for oceanic volcanic rocks representing both extremes of the range of mantle Hf-Nd-Sr isotopic variation. Hf from critical mid-ocean ridge basalts shows that 176Hf/177Hf does indeed have a greater variability than 143Nd/144Nd and 87Sr/86Sr in the depleted mantle. This extra variation is essentially of a random nature, and can perhaps be understood in terms of known Rb/Sr-Sm/Nd-Lu/Hf fractionation relationships. At the other extreme of mantle isotopic compositions, 176Hf/177Hf ratios for igneous rocks from the Indian Ocean island of Kerguelen show a closely similar variation to published 143Nd/144Nd ratios for the same samples. Comparison of Hf-Nd-Sr isotopic relatonships for Tristan da Cunha, Kerguelen and Samoa reveals divergences in the mantle array for ocean-island magma sources, and perhaps suggests that these irregularities are largely the result of an extra component of 87Sr/86Sr variation.-G.R.

  8. Sm-Nd and Rb-Sr isotopic systematics of the Pea Ridge Fe-P deposit and related rocks, southeast Missouri

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Marikos, M.A.; Barton, M.D.

    1993-03-01

    Pea ridge is a discordant Middle Proterozoic Fe-P deposit hosted in rhyolite tuffs and flows of the 1.4--1.5 Ga St. Francois terrane. Host rocks and the deposit are cut by basalt and aplite/pegmatite dikes. The deposit overlies a blind pluton which is partially surrounded by a trachytic ring complex. In the deposit, which is mined for Fe, early Qtz+Amph+Mag+Ap rock is cut by Mag+Ap+Qtz rock. Subsequently, portions of the deposit and host rocks were brecciated, oxidized and silicified to produce a complex suite of rocks enriched in Hem+Qtz+Ksp+Mu. Late breccia pipes/dikes cut the complex and were mineralized with Bar+Ksp+Flu+Chl+Cc+REE-phosphates. Sm/Ndmore » and Rb/Sr isotopic systematics have been studied to: (1) constrain source(s) of igneous rocks and deposit components, (2) refine ages of magmatism, mineralization, and later hydrothermal activity, (3) begin regional comparison of isotopic systematics in SE Missouri Fe deposits, and (4) complement ongoing Missouri DGLS/USGS studies. Fourteen combined Sm-Nd and Rb-Sr analyses were done on materials including two host rhyolites, two nearby trachytes, two gneiss samples representing plausible basement, two intramineral dikes, and six samples of mineralization.« less

  9. Age and origin of anorthosites, charnockites, and granulites in the Central Virginia Blue Ridge: Nd and Sr isotopic evidence

    USGS Publications Warehouse

    Pettingill, H.S.; Sinha, A.K.; Tatsumoto, M.

    1984-01-01

    Rb-Sr isotopic data for anorthosites, charnockites, ferrodioritic to quartz monzonitic plutons, and high-grade gneisses of the Blue Ridge of central Virginia show evidence of post-emplacement metamorphism, but in some cases retain Grenville ages. The Pedlar River Charnockite Suite yields an isochron age of 1021 +/-36 Ma, (initial 87Sr/86Sr ratio of 0.7047 +/-6), which agrees with published U-Pb zircon ages. Five samples of that unit which contain Paleozoic mylonitic fabrics define a regression line of 683 Ma, interpreted as a mixing line with no age significance. Samples of the Roseland Anorthosite Complex show excessive scatter on a Rb-Sr evolution diagram probably due to Paleozoic (475 m.y.) metamorphism. Data from the ferrodioritic to quartz monzonitic plutons of the area yield an age of 1009 +/-26 Ma (inital ratio=0.7058 +/-4), which is in the range of the U-Pb zircon ages of 1000-1100 Ma. The Stage Road Layered Gneiss yields an age of 1147 +/-34 Ma (initial ratio of 0.7047 +/- 5). Sm-Nd data for the Pedlar River Charnockite Suite reflect a pre-Grenville age of 1489 +/-118 Ma (e{open}Nd=+6.7 +/-1.2). Data for the Roseland Anorthosite Complex and the ferrodioritic to quartz monzonitic plutons yield Grenville isochron ages of 1045 +/44 Ma (e{open}Nd=+1.0 +/-0.3) and 1027 +/-101 Ma (e{open}Nd=+1.4 +/-1.0), respectively. Two Roseland Anorthosite samples plot far above the isochron, demonstrating the effects of post-emplacement disturbance of Sm-Nd systematics, while mylonitized Pedlar River Charnockite Suite samples show no evidence of Sm-Nd redistribution. The disparity of the Sm-Nd age and other isotopic ages for the Pedlar River Charnockite Suite probably reflects a Sm-Nd "source" age, suggesting the presence of an older crust within this portion of the ca. 1 Ga old basement. ?? 1984 Springer-Verlag.

  10. Nature and Significance of the High-Sr Aleutian Lavas

    NASA Astrophysics Data System (ADS)

    Yogodzinski, G. M.; Arndt, S.; Turka, J. R.; Kelemen, P. B.; Vervoort, J. D.; Portnyagin, M.; Hoernle, K.

    2011-12-01

    Results of the Western Aleutian Volcano Expedition and German-Russian KALMAR cruises include the discovery of seafloor volcanism at the Ingenstrem Depression and at unnamed seamounts 300 km west of Buldir, the westernmost emergent volcano in the Aleutian arc. These discoveries indicate that the surface expression of active Aleutian volcanism goes below sea level just west of Buldir, but is otherwise continuous along the full length of the arc. Many lavas dredged from western Aleutian seamounts are basalts, geochemically similar to basalts from elsewhere in Aleutians and other arcs (La/Yb 4-8, Sr/Y<30, 87Sr/86Sr=0.7031-0.7033). Western Aleutian dredge samples also include high-Sr lavas (>700 ppm Sr), which are mostly plagioclase-hornblende andesites and dacites with low Y and middle-heavy rare-earth elements, fractionated trace element patterns (Sr/Y=50-200, La/Yb=9-25) and MORB-like isotopes (87Sr/86Sr < 0.7028). The endmember Sr-rich lavas are magnesian rhyodacites (SiO2~68%, Mg# >0.65) with 1250-1700 ppm Sr, 4-7 ppm Y, low abundances of all rare-earth elements (La<7 ppm, Yb<0.4 ppm) and 87Sr/86Sr < 0.70266. The high silica and primitive (high Mg#) character of the high-Sr lavas, combined with their strongly fractionated trace element patterns and MORB-like isotopes are consistent with a source predominantly of subducted basalt and a melt residue that contained garnet. The high-Sr lavas have some characteristics of MORB fluids (low Ce/Pb and unradiogenic Pb), and their highly calc-alkaline nature implies high pre-eruptive water contents[1], but low 87Sr/86Sr indicates that their source was in MORB, not seawater-altered MORB. The high-Sr endmember is clearly present in andesites from some emergent volcanoes in the western Aleutians, and mixing arrays indicate that it may be present in all Aleutian lavas (e.g., 87Sr/86Sr vs. La/Yb or Sr/Y); however, radiogenic Pb and Sr from subducted sediment renders the high-Sr endmember isotopically invisible in most central and

  11. Sr-Nd-Pb isotopic constraints on the nature of the mantle sources involved in the genesis of the high-Ti tholeiites from northern Paraná Continental Flood Basalts (Brazil)

    NASA Astrophysics Data System (ADS)

    Rocha-Júnior, Eduardo R. V.; Marques, Leila S.; Babinski, Marly; Nardy, Antônio J. R.; Figueiredo, Ana M. G.; Machado, Fábio B.

    2013-10-01

    There has been little research on geochemistry and isotopic compositions in tholeiites of the Northern region from the Paraná Continental Flood Basalts (PCFB), one of the largest continental provinces of the world. In order to examine the mantle sources involved in the high-Ti (Pitanga and Paranapanema) basalt genesis, we studied Sr, Nd, and Pb isotopic systematics, and major, minor and incompatible trace element abundances. The REE patterns of the investigated samples (Pitanga and Paranapanema magma type) are similar (parallel to) to those of Island Arc Basalts' REE patterns. The high-Ti basalts investigated in this study have initial (133 Ma) 87Sr/86Sr ratios of 0.70538-0.70642, 143Nd/144Nd of 0.51233-0.51218, 206Pb/204Pb of 17.74-18.25, 207Pb/204Pb of 15.51-15.57, and 208Pb/204Pb of 38.18-38.45. These isotopic compositions do not display any correlation with Nb/Th, Nb/La or P2O5/K2O ratios, which also reflect that these rocks were not significantly affected by low-pressure crustal contamination. The incompatible trace element ratios and Sr-Nd-Pb isotopic compositions of the PCFB tholeiites are different to those found in Tristan da Cunha ocean island rocks, showing that this plume did not play a substantial role in the PCFB genesis. This interpretation is corroborated by previously published osmium isotopic data (initial γOs values range from +1.0 to +2.0 for high-Ti basalts), which also preclude basalt generation by melting of ancient subcontinental lithospheric mantle. The geochemical composition of the northern PCFB may be explained through the involvement of fluids and/or small volume melts related to metasomatic processes. In this context, we propose that the source of these magmas is a mixture of sublithospheric peridotite veined and/or interlayered with mafic components (e.g., pyroxenites or eclogites). The sublithospheric mantle (dominating the osmium isotopic compositions) was very probably enriched by fluids and/or magmas related to the

  12. Pb, Sr, and Nd isotopic compositions of a suite of Late Archean, igneous rocks, eastern Beartooth Mountains: implications for crust-mantle evolution

    USGS Publications Warehouse

    Wooden, J.L.; Mueller, P.A.

    1988-01-01

    A series of compositionally diverse, Late Archean rocks (2.74-2.79 Ga old) from the eastern Beartooth Mountains, Montana and Wyoming, U.S.A., have the same initial Pb, Sr, and Nd isotopic ratios. Lead and Sr initial ratios are higher and Nd initial ratios lower than would be expected for rocks derived from model mantle sources and strongly indicate the involvement of an older crustal reservoir in the genesis of these rocks. Crustal contamination during emplacement can be ruled out for a variety of reasons. Instead a model involving subduction of continental detritus and contamination of the overlying mantle as is often proposed for modern subduction environments is preferred. This contaminated mantle would have all the isotopic characteristics of mantle enriched by internal mantle metasomatism but would require no long-term growth or changes in parent to daughter element ratios. This contaminated mantle would make a good source for some of the Cenozoic mafic volcanics of the Columbia River, Snake River Plain, and Yellowstone volcanic fields that are proposed to come from ancient, enriched lithospheric mantle. The isotopic characteristics of the 2.70 Ga old Stillwater Complex are a perfect match for the proposed contaminated mantle which provides an alternative to crustal contamination during emplacement. The Pb isotopic characteristics of the Late Archean rocks of the eastern Beartooth Mountains are similar to those of other Late Archean rocks of the Wyoming Province and suggest that Early Archean, upper crustal rocks were common in this terrane. The isotopic signatures of Late Archean rocks in the Wyoming Province are distinctive from those of other Archean cratons in North America which are dominated by a MORB-like, Archean mantle source (Superior Province) and/or a long-term depleted crustal source (Greenland). ?? 1988.

  13. Pb sbnd Sr sbnd Nd isotopic data of Indian Ocean ridges: new evidence of large-scale mapping of mantle heterogeneities

    NASA Astrophysics Data System (ADS)

    Hamelin, Bruno; Dupré, Bernard; Allègre, Claude J.

    1986-01-01

    A Pb sbnd Sr sbnd Nd isotope study of South West and East Indian Ridges confirms that the Indian Ocean belongs to a specific regional isotopic domain, as previously suggested by the results from islands of this ocean. The isotopic domain defined by the Indian MORB is indeed different from that of the North Atlantic and East Pacific Oceans. This demonstrates that the convective circulation of the upper mantle does not allow a rapid homogenization from one region to the other. The isotopic data of the Indian ridges can be interpreted by a contamination model, in which the depleted upper mantle (identical to that under the North Atlantic) is contaminated by two different types of contaminant, one corresponding to the source of the "central Indian Ocean" islands (Amsterdam, St. Paul, Marion, Prince Edward, Réunion, Rodriguez, Mauritius), and the other to a source similar to that of Walvis or Ninety East aseismic ridges. These two contaminants would have contributed to the ridge volcanism in different proportions over time.

  14. Isotopic coherence of refractory inclusions from CV and CK meteorites: Evidence from multiple isotope systems

    NASA Astrophysics Data System (ADS)

    Shollenberger, Quinn R.; Borg, Lars E.; Render, Jan; Ebert, Samuel; Bischoff, Addi; Russell, Sara S.; Brennecka, Gregory A.

    2018-05-01

    Calcium-aluminum-rich inclusions (CAIs) are the oldest dated materials in the Solar System and numerous previous studies have revealed nucleosynthetic anomalies relative to terrestrial rock standards in many isotopic systems. However, most of the isotopic data from CAIs has been limited to the Allende meteorite and a handful of other CV3 chondrites. To better constrain the isotopic composition of the CAI-forming region, we report the first Sr, Mo, Ba, Nd, and Sm isotopic compositions of two CAIs hosted in the CK3 desert meteorites NWA 4964 and NWA 6254 along with two CAIs from the CV3 desert meteorites NWA 6619 and NWA 6991. After consideration of neutron capture processes and the effects of hot-desert weathering, the Sr, Mo, Ba, Nd, and Sm stable isotopic compositions of the samples show clearly resolvable nucleosynthetic anomalies that are in agreement with previous results from Allende and other CV meteorites. The extent of neutron capture, as manifested by shifts in the observed 149Sm-150Sm isotopic composition of the CAIs is used to estimate the neutron fluence experienced by some of these samples and ranges from 8.40 × 1013 to 2.11 × 1015 n/cm2. Overall, regardless of CAI type or host meteorite, CAIs from CV and CK chondrites have similar nucleosynthetic anomalies within analytical uncertainty. We suggest the region that CV and CK CAIs formed was largely uniform with respect to Sr, Mo, Ba, Nd, and Sm isotopes when CAIs condensed and that CAIs hosted in CV and CK meteorites are derived from the same isotopic reservoir.

  15. Petrogenesis of mid-Miocene rhyolites from the Idaho-Oregon-Nevada region, USA: Implications from feldspar Sr and Pb isotope data

    NASA Astrophysics Data System (ADS)

    Wypych, A.; Hart, W. K.

    2012-12-01

    The Idaho-Oregon-Nevada (ION) region provides an excellent natural laboratory for studying the complex processes that form continental crust. During the Oligocene-Miocene, the ION region underwent widespread extension and volcanism with bimodal (silicic and mafic) volcanism dominating the mid-Miocene [1]. This bimodal volcanism is temporally related to the main Columbia River flood basalt activity to the north, and initiated with mafic eruptions at ~17 Ma, followed closely by silicic magmatism at ~16.5 Ma. This intimate link between mafic and silicic activity continued until ~13 Ma. The ION region is situated on a boundary between Proterozoic cratonic lithosphere to the east and Mesozoic accreted terrains to the west as defined by Sr and Nd isotopic compositions. In this region, however, the boundary is not sharp and distinctive, but rather forms a heterogeneous "transitional zone" between the two lithospheric domains. Another feature adding to the complexity of this region is the fact that it lies at the junction of two major volcanic trends: the Snake River Plain- Yellowstone (SRP-Y) progressing in time and space to the northeast and the High Lava Plains - Newberry (HPL-N) progressing to the northwest. The ION region volcanism as well as the SRP-Y and HLP-N volcanic trends is caused by mantle upwelling behind the subducting Juan de Fuca slab, voluminous mafic magma injections into the crust, melting of spatially, temporally, and compositionally heterogeneous crust, and mixing of the primitive and more evolved products [1,2,3]. An ongoing petrographic, major and trace element and Sr-Nd-Pb-Hf isotope investigation of 24 pairs of glass separates and whole rock samples from five ION silicic centers representing a west (off-craton) to east (on-craton) transect across this zone of transitional lithosphere provides evidence of open system processes involved in the production of the silicic material as well as spatial, temporal and compositional diversity within and

  16. Hafnium isotope stratigraphy of ferromanganese crusts

    PubMed

    Lee; Halliday; Hein; Burton; Christensen; Gunther

    1999-08-13

    A Cenozoic record of hafnium isotopic compositions of central Pacific deep water has been obtained from two ferromanganese crusts. The crusts are separated by more than 3000 kilometers but display similar secular variations. Significant fluctuations in hafnium isotopic composition occurred in the Eocene and Oligocene, possibly related to direct advection from the Indian and Atlantic oceans. Hafnium isotopic compositions have remained approximately uniform for the past 20 million years, probably reflecting increased isolation of the central Pacific. The mechanisms responsible for the increase in (87)Sr/(86)Sr in seawater through the Cenozoic apparently had no effect on central Pacific deep-water hafnium.

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

    NASA Astrophysics Data System (ADS)

    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

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

    NASA Astrophysics Data System (ADS)

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

    2013-04-01

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

  19. H, O, Sr, Nd, and Pb isotope geochemistry of the Latir volcanic field and cogenetic intrusions, New Mexico, and relations between evolution of a continental magmatic center and modifications of the lithosphere

    USGS Publications Warehouse

    Johnson, C.M.; Lipman, P.W.; Czamanske, G.K.

    1990-01-01

    Over 200 H, O, Sr, Nd, and Pb isotope analyses, in addition to geologic and petrologic constraints, document the magmatic evolution of the 28.5-19 Ma Latir volcanic field and associated intrusive rocks, which includes multiple stages of crustal assimilation, magma mixing, protracted crystallization, and open- and closed-system evolution in the upper crust. In contrast to data from younger volcanic centers in northern New Mexico, relatively low and restricted primary ??18O values (+6.4 to +7.4) rule out assimilation of supracrustal rocks enriched in 18O. Initial 87Sr/86Sr ratios (0.705 to 0.708), ??18O values (-2 to-7), and 206Pb/204Pb ratios (17.5 to 18.4) of metaluminous precaldera volcanic rocks and postcaldera plutonic rocks suggest that most Latir rocks were generated by fractional crystallization of substantial volumes of mantle-derived basaltic magma that had near-chondritic Nd isotope ratios, accompanied by assimilation of crustal material in two main stages: 1) assimilation of non-radiogenic lower crust, followed by 2) assimilation of middle and upper crust by inter-mediate-composition magmas that had been contaminated during the first stage. Magmatic evolution in the upper crust peaked with eruption of the peralkaline Amalia Tuff (???26 Ma), which evolved from metaluminous parental magmas. A third stage of late, roofward assimilation of Proterozoic rocks in the Amalia Tuff magma is indicated by trends in initial 87Sr/86Sr and 206Pb/204Pb ratios from 0.7057 to 0.7098 and 19.5 to 18.8, respectively, toward the top of the pre-eruptive magma chamber. Highly evolved postcaldera plutons are generally fine grained and are zoned in initial 87Sr/86Sr and 206Pb/204Pb ratios, varying from 0.705 to 0.709 and 17.8 to 18.6, respectively. In contrast, the coarser-grained Cabresto Lake (???25 Ma) and Rio Hondo (???21 Ma) plutons have relatively homogeneous initial 87Sr/86Sr and 206Pb/204Pb ratios of approximately 0.7053 and 17.94 and 17.55, respectively. ??18O values for

  20. Zircon U-Pb geochronology and Sr-Nd-Pb-Hf isotopic constraints on the timing and origin of Mesozoic granitoids hosting the Mo deposits in northern Xilamulun district, NE China

    NASA Astrophysics Data System (ADS)

    Shu, Qihai; Lai, Yong; Zhou, Yitao; Xu, Jiajia; Wu, Huaying

    2015-12-01

    Located in the east section of the Central Asian orogen in northeastern China, the Xilamulun district comprises several newly discovered molybdenum deposits, primarily of porphyry type and Mesozoic ages. This district is divided by the Xilamulun fault into the southern and the northern parts. In this paper, we present new zircon U-Pb dating, trace elements and Hf isotope, and/or whole rock Sr-Nd-Pb isotopic results for the host granitoids from three Mo deposits (Yangchang, Haisugou and Shabutai) in northern Xilamulun. Our aim is to constrain the age and petrogenesis of these intrusions and their implications for Mo mineralization. Zircon U-Pb LA-ICP-MS dating shows that the monzogranites from the Shabutai and Yangchang deposits formed at 138.4 ± 1.5 and 137.4 ± 2.1 Ma, respectively, which is identical to the molybdenite Re-Os ages and coeval well with the other Mo deposits in this region, thereby indicating an Early Cretaceous magmatism and Mo mineralization event. Zircon Ce/Nd ratios from the mineralized intrusions are significantly higher than the barren granites, implying that the mineralization-related magmas are characterized by higher oxygen fugacity. These mineralized intrusions share similar zircon in-situ Hf and whole rock Sr-Nd isotopic compositions, with slightly negative to positive εHf(t) ranging from - 0.8 to + 10.0, restricted εNd(t) values from - 3.7 to + 1.6 but a little variable (87Sr/86Sr)i ratios between 0.7021 and 0.7074, indicative of formation from primary magmas generated from a dominantly juvenile lower crust source derived from depleted mantle, despite diverse consequent processes (e.g., magma mixing, fractional crystallization and crustal contamination) during their evolution. The Pb isotopes (whole rock) also show a narrow range of initial compositions, with (206Pb/204Pb)i = 18.03-18.88, (207Pb/204Pb)i = 15.48-15.58 and (208Pb/204Pb)i = 37.72-38.28, in agreement with Sr-Nd-Hf isotopes reflecting the dominance of a mantle component

  1. Helium-strontium isotope constraints on mantle evolution beneath the Roman Comagmatic Province, Italy

    NASA Astrophysics Data System (ADS)

    Martelli, M.; Nuccio, P. M.; Stuart, F. M.; Burgess, R.; Ellam, R. M.; Italiano, F.

    2004-08-01

    A study of the He isotopic ratios of fluid inclusions in olivine and pyroxene from the Roman Comagmatic Province (RCP), Italy, is presented together with 87Sr/ 86Sr isotope compositions of the whole rock or pyroxene phenocrysts. A clear covariation in He and Sr isotopes is apparent, with a strong northward increase in radiogenic He and Sr being evident. He and Sr isotopes ratios range from 3He/ 4He=5.2 Ra and 87Sr/ 86Sr=0.7056 in south Campania, to 3He/ 4He=0.44 Ra and 87Sr/ 86Sr=0.715905 in the northernmost Latium. Helium isotope ratios are significantly lower than MORB values and are among the lowest yet measured in subduction zone volcanism. The 3He/ 4He of olivine and pyroxene phenocryst-hosted volatiles appear to be little influenced by posteruptive processes and magma-crust interaction. The 3He/ 4He- 87Sr/ 86Sr covariation is consistent with binary mixing between an asthenospheric mantle similar to HIMU ocean island basalts, and an enriched (radiogenic) mantle end member generated from subduction of the Ionian/Adriatic plate. The contribution of radiogenic He from metasomatic fluids and postmetasomatism radiogenic ingrowth in the wedge is strongly dependent on the initial He concentration of the mantle. Only when asthenosphere He concentrations are substantially lower than the MORB source mantle, and metasomatism occurred at the beginning of the subduction (˜30 Ma), can ingrowth in the mantle wedge account for the 3He/ 4He of the most radiogenic basalts.

  2. Lu-Hf, in-situ Sr and Pb isotope and trace element systematics for mantle eclogites from the Diavik diamond mine: Evidence for Paleoproterozoic subduction beneath the Slave craton, Canada

    NASA Astrophysics Data System (ADS)

    Schmidberger, Stefanie S.; Simonetti, Antonio; Heaman, Larry M.; Creaser, Robert A.; Whiteford, Sean

    2007-02-01

    Lu-Hf, Sm-Nd and in-situ clinopyroxene Sr and Pb isotope systematics, and mineral major and in-situ trace element compositions were obtained for a suite of non-diamond and diamond-bearing eclogites from the Diavik kimberlites (A154; 55 Ma old), Slave craton (Canada). Temperature estimates of last equilibration in the lithosphere for the non-diamond-bearing Diavik eclogites define two groups; low-temperature (800-1050 °C) and high-temperature eclogites (1100-1300 °C). Most diamond-eclogites indicate temperatures similar to those of the high-temperature eclogites. Isotopic and major and trace element systematics for the non-diamond- and diamond-bearing eclogites indicate overlapping chemical compositions suggesting similar rock formational histories. Calculated whole rock major and trace element abundances using chemical and modal abundances for constituent minerals exhibit broad similarities with mafic cumulates from ophiolite sequences. Most importantly the calculated whole rock eclogite compositions display positive Sr and Eu anomalies, typically interpreted as the result of plagioclase accumulation in cumulate rocks of oceanic crust sequences. Initial whole rock Hf isotopic values and in-situ Sr isotope data from clinopyroxene grains provide evidence that the eclogites were derived from precursor rocks with depleted mantle isotope characteristics. These combined results support the interpretation that the eclogites from Diavik represent remnants of subducted oceanic crust. Lu-Hf isotope systematics indicate that the oceanic protolith for the eclogites formed in the Paleoproterozoic at ˜ 2.1 Ga, which is in agreement with the in-situ Pb isotope data from clinopyroxene. This result also corroborates the ˜ 2.1 Ga Lu-Hf model ages recorded by mantle zircons from eclogite found within the Jericho kimberlite in the northern Slave Province (˜ 200 km northwest of Diavik). The results from both studies indicate a link between eclogite formation and Paleoproterozoic

  3. Zircon U-Pb ages and Hf-O isotopes, and whole-rock Sr-Nd isotopes of the Bozhushan granite, Yunnan province, SW China: Constraints on petrogenesis and tectonic setting

    NASA Astrophysics Data System (ADS)

    Chen, Xiao-Cui; Hu, Rui-Zhong; Bi, Xian-Wu; Zhong, Hong; Lan, Jiang-Bo; Zhao, Cheng-Hai; Zhu, Jing-Jing

    2015-03-01

    The Bainiuchang silver-polymetallic ore deposit is a super-large deposit in the western part of the South China tungsten-tin province (or the Nanling tungsten-tin province). The deposit is spatially and temporally associated with the Bozhushan granite pluton. Our new data indicate that the Bozhushan granitoids formed at 86-87 Ma. The granitoids are geochemically consistent with A-type granite. The Bozhushan pluton consists predominantly of biotite granite that is characterized by weakly peraluminous to metaluminous compositions and high alkali contents (Na2O + K2O = 7.51-9.06 wt.%). The granitic rocks are enriched in large-ion lithophile elements (LILE) Rb, Th, U, and K, but relatively depleted in Ba and Sr. In addition, they have high Zr + Nb + Ce + Y contents (310-478 ppm) and high 10,000× Ga/Al ratios (2.7-3.1). The temperatures of the parental magmas for the Bozhushan granites are estimated to be 790-842 °C based on the zircon saturation thermometer. Isotopically, the Bozhushan granites are characterized by elevated initial 87Sr/86Sr ratios (0.7126-0.7257) and low εNd values (-11.2 to -12.4), and high δ18O values (7.91-9.58‰) and low εHf values (-9.5 to -6.1) for zircon crystals, which indicate a dominant continental crustal source. The two-stage Hf model ages vary from 1.53 to 1.86 Ga. The isotopic compositions support the interpretation that the granitic rocks formed by melting of the Meso- and Neoproterozoic metasedimentary basements of the Cathaysia block. These results, together with geological records in the other parts of the western Cathaysia block, suggest that the formation of the Bozhushan A-type granites is related to lithospheric extension and asthenospheric upwelling that are associated with the change of plate motion in Late-Cretaceous.

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

    USGS Publications Warehouse

    Rosenbauer, Robert J.; Foxgrover, Amy C.; Hein, James R.; Swarzenski, Peter W.; Barnard, P.L.; Jaffee, B.E.; Schoellhamer, D.H.

    2013-01-01

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

  5. Radiogenic isotopic approaches for quantifying radionuclide transport (Invited)

    NASA Astrophysics Data System (ADS)

    Maher, K.; Depaolo, D. J.; Singleton, M. J.; Christensen, J. N.; Conrad, M. E.

    2009-12-01

    Naturally occurring variations in the isotopic compositions of U and Sr provide unique opportunities for assessing the fate and transport of radionuclides at field-scale conditions. When coupled with reactive transport models, U and Sr isotopes may also provide additional constraints on the rates of sediment-fluid or sediment-waste interactions. Such isotopic approaches can be useful for sites where subsurface characterization is complicated by a lack of accessibility or the presence of substantial heterogeneity. In addition, a variety of quantitative modeling approaches of different complexity can be used to evaluate experimentally determined parameters for radionuclide mobility at the field-scale. At the Hanford Site in eastern Washington, 87Sr/86Sr and 234U/238U ratios have been used to quantify the residence time of Sr and U in the unsaturated zone, the long-term background infiltration rate through the unsaturated zone, and to assess the influence of enhanced wastewater discharge on the regional unconfined aquifer. As a result of different processing techniques or due to interactions between caustic waste and the natural sediment, waste plumes may also inherit isotopic fingerprints (e.g. 234U/238U, 235U/238U, 236U/238U; δ15N & δ18O of nitrate) that can be used to resolve multiple sources of contamination. Finally, enriched isotopic tracers can be applied to experimental manipulations to assess the retardation of a variety of contaminants. Collectively this isotopic data contributes unique perspectives on both the hydrologic conditions across the site and the mobility of key radionuclides. Predicting the long-term fate and transport of radionuclides in the environment is often challenging due to natural heterogeneity and incomplete characterization of the subsurface, however detailed analysis of isotopic variations can provide one additional means of characterizing the subsurface.

  6. The sources and time-integrated evolution of diamond-forming fluids - Trace elements and isotopic evidence

    NASA Astrophysics Data System (ADS)

    Klein-BenDavid, Ofra; Pearson, D. Graham; Nowell, Geoff M.; Ottley, Chris; McNeill, John C. R.; Logvinova, Alla; Sobolev, Nikolay V.

    2014-01-01

    Sub-micrometer inclusions in fibrous diamond growth zones carry high-density fluids (HDF) from which the host diamonds have precipitated. The chemistry of these fluids is our best opportunity of characterizing the diamond-forming environment. The major and trace element patterns of diamond-forming fluids vary widely. Such elemental signatures can be easily modified by a variety of mantle processes whereas radiogenic isotopes give a clear fingerprint of the time-integrated evolution of the fluid source region. Thus, the combination of elemental and isotope data is a powerful tool in constraining the origin of fluids from which diamonds precipitate. Here we present combined trace element composition (34 diamonds) and Sr isotopic data (23 diamonds) for fluid-rich diamonds from six worldwide locations. The Nd and Pb isotopic composition of two of the diamonds were also obtained. Several of the samples were analyzed in at least 2 locations to investigate variations in the fluid during diamond growth. The data was acquired using an off-line laser sampling technique followed by solution ICPMS and TIMS analysis. The Sr isotopic compositions of diamond fluids from the different suites range between convecting mantle values for Udachnaya (87Sr/86Sr363 = 0.70300 ± 16 to 0.70361 ± 4), to highly enriched values, up to 87Sr/86Sr = 0.72330 ± 3, for a diamond from Congo. No isochronous relationships were observed in any of the suites. The lowest Nd isotopic composition recorded so far in a diamond is from Congo (εNd71 = -40.4), which also contains the most radiogenic Sr isotopic composition. In contrast, a less enriched but still rather unradiogenic Nd isotope composition (εNd540 = -11) was obtained for a diamond from Snap Lake, which has moderately radiogenic Sr isotopic enrichment (87Sr/86Sr540 = 0.70821 ± 1). The Pb isotopic system measured in one diamond indicates a complex evolution for the fluid source, with extreme 207Pb/204Pb ratio (15.810 ± 3) and moderate

  7. Structure in the secular variation of seawater sup 87 Sr/ sup 86 Sr for the Ivorian/Chadian (Osagean, Lower Carboniferous)

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Douthit, T.L.; Hanson, G.N.; Meyers, W.J.

    1990-05-01

    The secular variations of {sup 87}Sr/{sup 86}Sr in seawater for the Ivorian/Chadian, (equivalent to the Osagean, Lower Carboniferous) were determined through detailed analysis of well-preserved marine cements from the Waulsortian facies of Ireland. The results indicate that marine cements have utility in characterizing marine paleochemistries. Marine cements were judged pristine on the basis of nonluminescent character and stable isotopic composition comparable to previous estimates of Mississippian marine calcite. Analysis of the marine cements yielded {sup 87}Sr/{sup 86}Sr ratios lower than previously reported values for the Ivorian/Chadian. Error resulting from chronostratigraphic correlation between different geographic areas was avoided by restricting themore » sample set to a single 1,406-ft-long core (core P-1). The P-1 core is estimated to represent a minimum of 8.7 m.y. of continuous Waulsortian Limestone deposition. The {sup 87}Sr/{sup 86}Sr ratios of 11 nonluminescent cements document a non-monotonic variation in seawater {sup 87}Sr/{sup 86}Sr along the length of the core. {sup 87}Sr/{sup 86}Sr ranges from a high of 0.707908 in the early Ivorian to a low of about 0.707650 in the late Ivorian and middle Chadian with an early Chadian maximum at 0.707800 (all data are adjusted to a value of 0.710140 for SRM 987). The indicated maximum rate of change in seawater {sup 87}Sr/{sup 86}Sr is {minus}0.00011/Ma, comparable in magnitude to Tertiary values. The secular variation curve of seawater {sup 87}Sr/{sup 86}Sr for the Ivorian/Chadian has previously been thought to decrease monotonically with decreasing age. These data suggest that the seawater {sup 87}Sr/{sup 86}Sr variation over this interval may be sinusoidal in nature and emphasize the importance of well-characterized intraformational isotopic base lines.« less

  8. Sr, Nd and Pb isotopes in Proterozoic intrusives astride the Grenville Front in Labrador: Implications for crustal contamination and basement mapping

    USGS Publications Warehouse

    Ashwal, L.D.; Wooden, J.L.; Emslie, R.F.

    1986-01-01

    We report Sr, Nd and Pb isotopic compositions of mid-Proterozoic anorthosites and related rocks (1.45-1.65 Ga) and of younger olivine diabase dikes (1.4 Ga) from two complexes on either side of the Grenville Front in Labrador. Anorthositic or diabasic samples from the Mealy Mountains (Grenville Province) and Harp Lake (Nain-Churchill Provinces) complexes have very similar major, minor and trace element compositions, but distinctly different isotopic signatures. All Mealy Mountains samples have ISr = 0.7025-0.7033, ??{lunate}Nd = +0.6 to +5.6 and Pb isotopic compositions consistent with derivation from a mantle source depleted with respect to Nd/Sm and Rb/Sr. Pb isotopic compositions for the Mealy Mountains samples are slightly more radiogenic than model mantle compositions. All Harp Lake samples have ISr = 0.7032-0.7066, ??{lunate}Nd = -0.3 to -4.4 and variable, but generally unradiogenic 207Pb 204Pb and 206Pb 204Pb compared to model mantle, suggesting mixing between a mantle-derived component and a U-depleted crustal contaminant. Crustal contaminants are probably a variety of Archean high-grade quartzofeldspathic gneisses with low U/Pb ratios and include a component that must be isotopically similar to the early Archean (>3.6 Ga) Uivak gneisses of Labrador or the Amitsoq gneisses of west Greenland. This would imply that the ancient gneiss complex of coastal Labrador and Greenland is larger than indicated by present surface exposure and may extend in the subsurface as far west as the Labrador Trough. If Harp Lake and Mealy Mountains samples were subjected to the same degree of contamination, as suggested by their chemical similarities, then the Mealy contaminants must be much younger, probably early or middle Proterozoic in age. The Labrador segment of the Grenville Front, therefore, appears to coincide with the southern margin of the Archean North Atlantic craton and may represent a pre mid-Proterozoic suture. ?? 1986.

  9. Assessment of 137Cs and 90Sr Fluxes in the Barents Sea

    NASA Astrophysics Data System (ADS)

    Matishov, Gennady; Usiagina, Irina; Kasatkina, Nadezhda; Ilin, Gennadii

    2014-05-01

    On the basis of published and own data the annual balance of radionuclide income/outcome was assessed for 137Cs and 90Sr in the Barents Sea for the period from 1950s to the presnt. The scheme of the isotope balance calculation in the Barents Sea included the following processes:atmospheric fallout; river run-off; liquid radioactive wastes releases, income from the Norwegian and the White Seas; outflow to the adjacent areas through the Novaya Zemlya straits and the transects Svalbard-Franz Josef Land and Franz Josef Land-Novaya Zemlya; radioactive decay. According to the multiyear dynamics, the inflow of 137Cs and 90Sr to the Barents Sea was significantly preconditioned by currents from the Norwegian Sea. Three peaks of 137Cs and 90Sr isotope concentrations were registered for the surface waters on the western border of the Barents Sea. The first one was observed in the mid-1960s and was conditioned by testing of nuclear weapons. The increase of isotope concentrations in 1975 and 1980 was preconditioned by the discharge of atomic waste by the Sellafield nuclear reprocessing plant. Nowadays, after the sewage disposal plant was built, the annual discharge of nuclear waste from Sellafield plant is low. The Norwegian Sea was a major source of 137Cs and 90Sr isotope income into the Barents Sea for the period of 1960-2014. Currently, the transborder transfer of 90Sr and 137Cs from the Norwegian Sea into the Barents Sea constitutes about 99% of income for each element. Atmospheric precipitation had a major impact in the 1950-1960s after the testing of the nuclear weapons, and in 1986 after the accident at Chernobyl Nuclear Power Station. In 1963, the atmospheric precipitation of 137Cs reached 1050 TBq; and that of 90Sr, 630 TBq. In 1986, a significant amount of 137Cs inflow (up to 1010 TBq/year) was registered. The 137Cs isotope income exceeded the 90Sr income in the 1960s-1980s, and equal amounts penetrated into the Barents Sea from the Norwegian Sea in the 1990s. Before

  10. Sm-Nd and Rb-Sr Ages for MIL 05035: Implications for Surface and Mantle Sources

    NASA Technical Reports Server (NTRS)

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

    2007-01-01

    The Sm-Nd and Rb-Sr ages and also the initial Nd and Sr isotopic compositions of MIL 05035 are the same as those of A-881757. Comparing the radiometric ages of these meteorites to lunar surface ages as modeled from crater size-frequency distributions as well as the TiO2 abundances and initial Sr-isotopic compositions of other basalts places their likely place of origin as within the Australe or Humboldtianum basins. If so, a fundamental west-east lunar asymmetry in compositional and isotopic parameters that likely is due to the PKT is implied.

  11. Decoupling of Mg-C and Sr-Nd-O isotopes traces the role of recycled carbon in magnesiocarbonatites from the Tarim Large Igneous Province

    NASA Astrophysics Data System (ADS)

    Cheng, Zhiguo; Zhang, Zhaochong; Hou, Tong; Santosh, M.; Chen, Lili; Ke, Shan; Xu, Lijuan

    2017-04-01

    The Tarim Large Igneous Province in NW China hosts numerous magmatic carbonatite dikes along its northern margin. The carbonatites are composed mainly of dolomite (90 vol.%) and minor calcite (5 vol.%), with apatite, barite, celestine, aegirine, monazite and bastnaesite as accessory minerals. The rocks correspond to magnesiocarbonatites with a compositional range of 13.73-19.59 wt.% MgO, and 20.03-30.11 wt.% CaO, along with 1.65-3.31 wt.% total Fe2O3, 0.02-2.39 wt.% SiO2 and other minor elements, such as P2O5, Na2O and K2O. These magnesiocarbonatites are characterized by extreme enrichment in incompatible elements with high total rare earth element (REE) contents of 372-36965 ppm. The strontium [(87Sr/86Sr)i = 0.70378-0.70386], neodymium [εNd(t) = +2.51 - +3.59] and oxygen (δ18OV-SMOW = 5.9‰-8.0‰) isotope values of these rocks are consistent with a mantle origin, whereas the magnesium (δ26Mg = -1.09‰ to -0.85‰) and carbon (δ13CV-PDB = -4.1‰ to -5.9‰) isotopes are decoupled from mantle values and reflect signature of recycled sedimentary carbonates. Global plate tectonic models predict that sedimentary carbonates in convergent margins are subducted to deep domains in the mantle, with phase transitions from calcite/dolomite to magnesite, and eventually to periclase/perovskite. The involvement of a mantle plume enhances the normal mantle geotherms and promotes decomposition reactions of magnesite. The decoupling of Mg-C and Sr-Nd-O isotopes in the mangesiocarbonatites provides insights on the origin of carbonatites, and also illustrates a case of interaction between mantle plume and subduction-related components.

  12. Nd, Sr, and O isotopic variations in metaluminous ash-flow tuffs and related volcanic rocks at the Timber Mountain/Oasis Valley Caldera, Complex, SW Nevada: implications for the origin and evolution of large-volume silicic magma bodies

    USGS Publications Warehouse

    Farmer, G.L.; Broxton, D.E.; Warren, R.G.; Pickthorn, W.

    1991-01-01

    Nd, Sr and O isotopic data were obtained from silicic ash-flow tuffs and lavas at the Tertiary age (16-9 Ma) Timber (Mountain/Oasis Valley volcanic center (TMOV) in southern Nevada, to assess models for the origin and evolution of the large-volume silicic magma bodies generated in this region. The large-volume (>900 km3), chemically-zoned, Topopah Spring (TS) and Tiva Canyon (TC) members of the Paintbrush Tuff, and the Rainier Mesa (RM) and Ammonia Tanks (AT) members of the younger Timber Mountain Tuff all have internal Nd and Sr isotopic zonations. In each tuff, high-silica rhyolites have lower initial e{open}Nd values (???1 e{open}Nd unit), higher87Sr/86Sr, and lower Nd and Sr contents, than cocrupted trachytes. The TS, TC, and RM members have similar e{open}Nd values for high-silica rhyolites (-11.7 to -11.2) and trachytes (-10.5 to -10.7), but the younger AT member has a higher e{open}Nd for both compositional types (-10.3 and -9.4). Oxygen isotope data confirm that the TC and AT members were derived from low e{open}Nd magmas. The internal Sr and Nd isotopic variations in each tuff are interpreted to be the result of the incorporation of 20-40% (by mass) wall-rock into magmas that were injected into the upper crust. The low e{open}Nd magmas most likely formed via the incorporation of low ??18O, hydrothermally-altered, wall-rock. Small-volume rhyolite lavas and ash-flow tuffs have similar isotopic characteristics to the large-volume ash-flow tuffs, but lavas erupted from extracaldera vents may have interacted with higher ??18O crustal rocks peripheral to the main magma chamber(s). Andesitic lavas from the 13-14 Ma Wahmonie/Salyer volcanic center southeast of the TMOV have low e{open}Nd (-13.2 to -13.8) and are considered on the basis of textural evidence to be mixtures of basaltic composition magmas and large proportions (70-80%) of anatectic crustal melts. A similar process may have occurred early in the magmatic history of the TMOV. The large-volume rhyolites

  13. Use of 87Sr/86Sr and δ11B to Identify Slag-Affected Sediment in Southern Lake Michigan

    USGS Publications Warehouse

    Bayless, E. Randall; Bullen, Thomas D.; Fitzpatrick, John A.

    2004-01-01

    Slag is a ubiquitous byproduct of the iron-smelting industry and influences geochemistry and water quality in adjacent geologic units, ground and surface water. Despite extensive slag deposition along the Indiana shoreline of Lake Michigan, definitive evidence that slag has affected lakebed sediments has not been established. Concerns for the protection of water and ecosystem resources in the Great Lakes motivated this study to determine if strontium and boron isotopes could be used to identify and delineate slag-affected bed sediment in Lake Michigan. Sixty-five samples of bed sediment were acquired from the southern lobe of Lake Michigan and analyzed for 87Sr/86Sr and ??11B. Samples immediately offshore from Indiana steel mills and slag-disposal sites contained higher median 87Sr/86Sr values (0.70881) than shoreline sediments collected elsewhere in the basin (0.70847) and uniquely decreased with increasing distance from the shoreline. The highest ??11B values occurred in sediments from the Indiana shoreline (+12.9 to 16.4???) but were also elevated in sediments collected offshore from three Lake Michigan cities (+11.7 to 12.7???). Contoured isotope data indicated that 82-154 km2 of bed sediment along the Indiana shoreline had elevated 87Sr/86Sr and ??11B values relative to shoreline sediments elsewhere in southern Lake Michigan.

  14. 87Sr/88Sr a useful tool for the identification of geographic origin of Styrian pumpkin seed oils?

    NASA Astrophysics Data System (ADS)

    Meisel, T.; Bandoniene, D.; Zettl, D.; Maneiko, M.; Horschinegg, M.

    2012-04-01

    The authenticity and the geographic origin of Styrian pumpkin seed oil (PGI) a regional specialty needs to be protected, but the current specification of this high priced product does not include the proof of origin through analytical tools. As it turns out, this and many other products within the Protected Geographical Status (PGS) framework of the European Union, cannot be protected from fraud without forensic tools. In previous studies we were able to demonstrate, that distribution and content of trace elements in particular the rare earth elements, are useful parameters to discriminate Austrian from non-Austrian pumpkin seed oils and seeds. Unlike stable isotopes ratios (C and H), the trace element patterns are not influenced by changes in weather conditions and temperature during growing and harvesting cycle. Though the study of the distribution of element traces can be used not only for the identification of the geographic origin with very useful PLS and PCA models but also can identify fraud through mixing with other oils, this method need to be validated by other means. Radiogenic isotopes, in particular the 87Sr/86Sr isotope amount ratio has been successfully applied to food and other products for forensic studies. In this study we determined the 87Sr/86Sr isotope amount ratio in pumpkin seed oils extracted from seeds of known geographic origin from Austria, Russia and China, as these are the largest producers, to see if significant differences occur and if they can be used as a forensic tool. Although the total area of the Russian and the Chinese crop fields are magnitudes larger than the ones from Austria, it turns out that the variance of the Austrian 87Sr/86Sr data is much larger than that from other sources. Reasons are the large diversity of the Austrian geology (pre-varsican, alpine to sub-recent ages of the underlying bedrock of the soils can be found), the small farm sizes and the small scale production. In Russia large farms are situated on

  15. Calibration of amino acid racemization (AAR) kinetics in United States mid-Atlantic Coastal Plain Quaternary mollusks using 87Sr/ 86Sr analyses: Evaluation of kinetic models and estimation of regional Late Pleistocene temperature history

    USGS Publications Warehouse

    Wehmiller, J.F.; Harris, W.B.; Boutin, B.S.; Farrell, K.M.

    2012-01-01

    The use of amino acid racemization (AAR) for estimating ages of Quaternary fossils usually requires a combination of kinetic and effective temperature modeling or independent age calibration of analyzed samples. Because of limited availability of calibration samples, age estimates are often based on model extrapolations from single calibration points over wide ranges of D/L values. Here we present paired AAR and 87Sr/ 86Sr results for Pleistocene mollusks from the North Carolina Coastal Plain, USA. 87Sr/ 86Sr age estimates, derived from the lookup table of McArthur et al. [McArthur, J.M., Howarth, R.J., Bailey, T.R., 2001. Strontium isotopic stratigraphy: LOWESS version 3: best fit to the marine Sr-isotopic curve for 0-509 Ma and accompanying Look-up table for deriving numerical age. Journal of Geology 109, 155-169], provide independent age calibration over the full range of amino acid D/L values, thereby allowing comparisons of alternative kinetic models for seven amino acids. The often-used parabolic kinetic model is found to be insufficient to explain the pattern of racemization, although the kinetic pathways for valine racemization and isoleucine epimerization can be closely approximated with this function. Logarithmic and power law regressions more accurately represent the racemization pathways for all amino acids. The reliability of a non-linear model for leucine racemization, developed and refined over the past 20 years, is confirmed by the 87Sr/ 86Sr age results. This age model indicates that the subsurface record (up to 80m thick) of the North Carolina Coastal Plain spans the entire Quaternary, back to ???2.5Ma. The calibrated kinetics derived from this age model yield an estimate of the effective temperature for the study region of 11??2??C., from which we estimate full glacial (Last Glacial Maximum - LGM) temperatures for the region on the order of 7-10??C cooler than present. These temperatures compare favorably with independent paleoclimate information

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

    PubMed

    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.

  17. High Throughput Strontium Isotope Method for Monitoring Fluid Flow Related to Geological CO2 Storage

    NASA Astrophysics Data System (ADS)

    Capo, R. C.; Wall, A. J.; Stewart, B. W.; Phan, T. T.; Jain, J. C.; Hakala, J. A.; Guthrie, G. D.

    2012-12-01

    Natural isotope tracers, such as strontium (Sr), can be a unique and powerful component of a monitoring strategy at a CO2 storage site, facilitating both the quantification of reaction progress for fluid-rock interactions and the tracking of brine migration caused by CO2 injection. Several challenges must be overcome, however, to enable the routine use of isotopic tracers, including the ability to rapidly analyze numerous aqueous samples with potentially complex chemical compositions. In a field situation, it might be necessary to analyze tens of samples over a short period of time to identify subsurface reactions and respond to unexpected fluid movement in the host formation. These conditions require streamlined Sr separation chemistry for samples ranging from pristine groundwaters to those containing high total dissolved solids, followed by rapid measurement of isotope ratios with high analytical precision. We have optimized Sr separation chemistry and MC-ICP-MS methods to provide rapid and precise measurements of isotope ratios in geologic, hydrologic, and environmental samples. These improvements will allow an operator to independently prepare samples for Sr isotope analysis off-site using fast, low cost chemical separation procedures and commercially available components. Existing vacuum-assisted Sr separation procedures were modified by using inexpensive disposable parts to eliminate cross contamination. Experimental results indicate that the modified columns provide excellent separation of Sr from chemically complex samples and that Sr can be effectively isolated from problematic matrix elements (e.g., Ca, Ba, K) associated with oilfield brines and formation waters. The separation procedure is designed for high sample throughput in which batches of 24 samples can be processed in approximately 2 hours, and are ready for Sr isotope measurements by MC-ICP-MS immediately after collection from the columns. Precise Sr isotope results can be achieved by MC

  18. Modelling the Phanerozoic carbon cycle and climate: constraints from the 87Sr/86Sr isotopic ratio of seawater

    NASA Technical Reports Server (NTRS)

    Francois, L. M.; Walker, J. C.

    1992-01-01

    A numerical model describing the coupled evolution of the biogeochemical cycles of carbon, sulfur, calcium, magnesium, phosphorus, and strontium has been developed to describe the long-term changes of atmospheric carbon dioxide and climate during the Phanerozoic. The emphasis is on the effects of coupling the cycles of carbon and strontium. Various interpretations of the observed Phanerozoic history of the seawater 87Sr/86Sr ratio are investigated with the model. More specifically, the abilities of continental weathering, volcanism, and surface lithology in generating that signal are tested and compared. It is suggested that the observed fluctuations are mostly due to a changing weatherability over time. It is shown that such a conclusion is very important for the modelling of the carbon cycle. Indeed, it implies that the conventional belief that the evolution of atmospheric carbon dioxide and climate on a long time scale is governed by the balance between the volcanic input of CO2 and the rate of silicate weathering is not true. Rather carbon exchanges between the mantle and the exogenic system are likely to have played a key role too. Further, the increase of the global weathering rates with increasing surface temperature and/or atmospheric CO2 pressure usually postulated in long-term carbon cycle and climate modelling is also inconsistent with the new model. Other factors appear to have modulated the weatherability of the continents through time, such as mountain building and the existence of glaciers and ice sheets. Based on these observations, a history of atmospheric carbon dioxide and climate during Phanerozoic time, consistent with the strontium isotopic data, is reconstructed with the model and is shown to be compatible with paleoclimatic indicators, such as the timing of glaciation and the estimates of Cretaceous paleotemperatures.

  19. Matrix Effects Originating from Coexisting Minerals and Accurate Determination of Stable Silver Isotopes in Silver Deposits.

    PubMed

    Guo, Qi; Wei, Hai-Zhen; Jiang, Shao-Yong; Hohl, Simon; Lin, Yi-Bo; Wang, Yi-Jing; Li, Yin-Chuan

    2017-12-19

    Except for extensive studies in core formation and volatile-element depletion processes using radiogenic Ag isotopes (i.e., the Pd-Ag chronometer), recent research has revealed that the mass fractionation of silver isotopes is in principle controlled by physicochemical processes (e.g., evaporation, diffusion, chemical exchange, etc.) during magmatic emplacement and hydrothermal alteration. As these geologic processes only produce very minor variations of δ 109 Ag from -0.5 to +1.1‰, more accurate and precise measurements are required. In this work, a robust linear relationship between instrumental mass discrimination of Ag and Pd isotopes was obtained at the Ag/Pd molar ratio of 1:20. In Au-Ag ore deposits, silver minerals have complex paragenetic relationships with other minerals (e.g., chalcopyrite, sphalerite, galena, pyrite, etc.). It is difficult to remove such abundant impurities completely because the other metals are tens to thousands of times richer than silver. Both quantitative evaluation of matrix effects and modification of chemical chromatography were carried out to deal with the problems. Isobaric inferences (e.g., 65 Cu 40 Ar + to 105 Pd, 208 Pb 2+ to 104 Pd, and 67 Zn 40 Ar + to 107 Ag + ) and space charge effects dramatically shift the measured δ 109 Ag values. The selection of alternative Pd isotope pairs is effective in eliminating spectral matrix effects so as to ensure accurate analysis under the largest possible ranges for metal impurities, which are Cu/Ag ≤ 50:1, Fe/Ag ≤ 600:1, Pb/Ag ≤ 10:1, and Zn/Ag ≤ 1:1, respectively. With the modified procedure, we reported silver isotope compositions (δ 109 Ag) in geological standard materials and typical Au-Ag ore deposit samples varying from -0.029 to +0.689 ‰ with external reproducibility of ±0.009-0.084 ‰. A systemic survey of δ 109 Ag (or ε 109 Ag) variations in rocks, ore deposits, and environmental materials in nature is discussed.

  20. Carboniferous climate teleconnections archived in coupled bioapatite δ18OPO4 and 87Sr/86Sr records from the epicontinental Donets Basin, Ukraine

    NASA Astrophysics Data System (ADS)

    Montañez, Isabel P.; Osleger, Dillon J.; Chen, Jitao; Wortham, Barbara E.; Stamm, Robert G.; Nemyrovska, Tamara I.; Griffin, Julie M.; Poletaev, Vladislav I.; Wardlaw, Bruce R.

    2018-06-01

    Reconstructions of paleo-seawater chemistry are largely inferred from biogenic records of epicontinental seas. Recent studies provide considerable evidence for large-scale spatial and temporal variability in the environmental dynamics of these semi-restricted seas that leads to the decoupling of epicontinental isotopic records from those of the open ocean. We present conodont apatite δ18OPO4 and 87Sr/86Sr records spanning 24 Myr of the late Mississippian through Pennsylvanian derived from the U-Pb calibrated cyclothemic succession of the Donets Basin, eastern Ukraine. On a 2 to 6 Myr-scale, systematic fluctuations in bioapatite δ18OPO4 and 87Sr/86Sr broadly follow major shifts in the Donets onlap-offlap history and inferred regional climate, but are distinct from contemporaneous more open-water δ18OPO4 and global seawater Sr isotope trends. A -1 to -6‰ offset in Donets δ18OPO4 values from those of more open-water conodonts and greater temporal variability in δ18OPO4 and 87Sr/86Sr records are interpreted to primarily record climatically driven changes in local environmental processes in the Donets sea. Systematic isotopic shifts associated with Myr-scale sea-level fluctuations, however, indicate an extrabasinal driver. We propose a mechanistic link to glacioeustasy through a teleconnection between high-latitude ice changes and atmospheric pCO2 and regional monsoonal circulation in the Donets region. Inferred large-magnitude changes in Donets seawater salinity and temperature, not archived in the more open-water or global contemporaneous records, indicate a modification of the global climate signal in the epicontinental sea through amplification or dampening of the climate signal by local and regional environmental processes. This finding of global climate change filtered through local processes has implications for the use of conodont δ18OPO4 and 87Sr/86Sr values as proxies of paleo-seawater composition, mean temperature, and glacioeustasy.

  1. Carboniferous climate teleconnections archived in coupled bioapatite δ18OPO4 and 87Sr/86Sr records from the epicontinental Donets Basin, Ukraine

    USGS Publications Warehouse

    Montanez, Isabel P.; Osleger, Dillon J.; Chen, J.-H.; Wortham, Barbara E.; Stamm, Robert G.; Nemyrovska, Tamara I.; Griffin, Julie M.; Poletaev, Vladislav I.; Wardlaw, Bruce R.

    2018-01-01

    Reconstructions of paleo-seawater chemistry are largely inferred from biogenic records of epicontinental seas. Recent studies provide considerable evidence for large-scale spatial and temporal variability in the environmental dynamics of these semi-restricted seas that leads to the decoupling of epicontinental isotopic records from those of the open ocean. We present conodont apatite δ18OPO4 and 87Sr/86Sr records spanning 24 Myr of the late Mississippian through Pennsylvanian derived from the U–Pb calibrated cyclothemic succession of the Donets Basin, eastern Ukraine. On a 2 to 6 Myr-scale, systematic fluctuations in bioapatite δ18OPO4 and 87Sr/86Sr broadly follow major shifts in the Donets onlap–offlap history and inferred regional climate, but are distinct from contemporaneous more open-water δ18OPO4 and global seawater Sr isotope trends. A −1 to −6‰ offset in Donets δ18OPO4 values from those of more open-water conodonts and greater temporal variability in δ18OPO4 and 87Sr/86Sr records are interpreted to primarily record climatically driven changes in local environmental processes in the Donets sea. Systematic isotopic shifts associated with Myr-scale sea-level fluctuations, however, indicate an extrabasinal driver. We propose a mechanistic link to glacioeustasy through a teleconnection between high-latitude ice changes and atmospheric pCO2 and regional monsoonal circulation in the Donets region. Inferred large-magnitude changes in Donets seawater salinity and temperature, not archived in the more open-water or global contemporaneous records, indicate a modification of the global climate signal in the epicontinental sea through amplification or dampening of the climate signal by local and regional environmental processes. This finding of global climate change filtered through local processes has implications for the use of conodont δ18OPO4 and 87Sr/86Sr values as proxies of paleo-seawater composition, mean temperature, and glacioeustasy.

  2. Constraints on Late Paleozoic Ocean Response to Climate Change Based on Brachiopod δ11B and 87Sr/86Sr

    NASA Astrophysics Data System (ADS)

    Legett, S. A.; Rasbury, T.; Grossman, E. L.; Hemming, G.

    2017-12-01

    In order to understand the possible effects of climate change on present day oceans, it is important to determine how marine systems responded to climate change in the past. This study uses δ11B values from well-preserved Carboniferous and Permian brachiopods as well as models to examine chemical trends in seawater and how these relate to long- and short-term climate changes. Our results show that δ11B rises rapidly going into the Carboniferous from a low of 10‰ to a high of 17‰ and remains relatively stable through the Carboniferous, despite the initiation of glaciation in the Mid Carboniferous. At the Carboniferous-Permian boundary, δ11B declines into the Early Permian before reaching a low at the Sakmarian. This decline in δ11B is coincident with the decrease in 87Sr/86Sr through this interval, which corresponds to evidence for aridity going into the Permian. We hypothesize that a reduction in silicate weathering drives an increase in atmospheric pCO2 and a subsequent lowering of ocean pH going into the Permian. This is consistent with our interpretation of the Carboniferous-Permian boundary, as a major mechanism for controlling seawater boron isotope composition is the adsorption of borate on clays, removing isotopically light boron and thus leaving seawater boron isotopically heavy. Therefore, at lower pH seawater should become isotopically lighter as this mechanism for removal is reduced. These hypotheses are supported by our initial modeling results of the B and Sr isotopic budgets of the ocean during the Late Paleozoic.

  3. High-precision measurement of variations in calcium isotope ratios in urine by multiple collector inductively coupled plasma mass spectrometry

    USGS Publications Warehouse

    Morgan, J.L.L.; Gordon, G.W.; Arrua, R.C.; Skulan, J.L.; Anbar, A.D.; Bullen, T.D.

    2011-01-01

    We describe a new chemical separation method to isolate Ca from other matrix elements in biological samples, developed with the long-term goal of making high-precision measurement of natural stable Ca isotope variations a clinically applicable tool to assess bone mineral balance. A new two-column procedure utilizing HBr achieves the purity required to accurately and precisely measure two Ca isotope ratios (44Ca/42Ca and 44Ca/43Ca) on a Neptune multiple collector inductively coupled plasma mass spectrometer (MC-ICPMS) in urine. Purification requirements for Sr, Ti, and K (Ca/Sr > 10000; Ca/Ti > 10000000; and Ca/K > 10) were determined by addition of these elements to Ca standards of known isotopic composition. Accuracy was determined by (1) comparing Ca isotope results for samples and standards to published data obtained using thermal ionization mass spectrometry (TIMS), (2) adding a Ca standard of known isotopic composition to a urine sample purified of Ca, and (3) analyzing mixtures of urine samples and standards in varying proportions. The accuracy and precision of δ44/42Ca measurements of purified samples containing 25 μg of Ca can be determined with typical errors less than ±0.2‰ (2σ).

  4. Crustal contamination and crystal entrapment during polybaric magma evolution at Mt. Somma-Vesuvius volcano, Italy: Geochemical and Sr isotope evidence

    USGS Publications Warehouse

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

    2006-01-01

    New major and trace element analyses and Sr-isotope determinations of rocks from Mt. Somma-Vesuvius volcano produced from 25 ky BP to 1944 AD are part of an extensive database documenting the geochemical evolution of this classic region. Volcanic rocks include silica undersaturated, potassic and ultrapotassic lavas and tephras characterized by variable mineralogy and different crystal abundance, as well as by wide ranges of trace element contents and a wide span of initial Sr-isotopic compositions. Both the degree of undersaturation in silica and the crystal content increase through time, being higher in rocks produced after the eruption at 472 AD (Pollena eruption). Compositional variations have been generally thought to reflect contributions from diverse types of mantle and crust. Magma mixing is commonly invoked as a fundamental process affecting the magmas, in addition to crystal fractionation. Our assessment of geochemical and Sr-isotopic data indicates that compositional variability also reflects the influence of crustal contamination during magma evolution during upward migration to shallow crustal levels and/or by entrapment of crystal mush generated during previous magma storage in the crust. Using a variant of the assimilation fractional crystallization model (Energy Conservation-Assimilation Fractional Crystallization; [Spera and Bohrson, 2001. Energy-constrained open-system magmatic processes I: General model and energy-constrained assimilation and fractional crystallization (EC-AFC) formulation. J. Petrol. 999-1018]; [Bohrson, W.A. and Spera, F.J., 2001. Energy-constrained open-system magmatic process II: application of energy-constrained assimilation-fractional crystallization (EC-AFC) model to magmatic systems. J. Petrol. 1019-1041]) we estimated the contributions from the crust and suggest that contamination by carbonate rocks that underlie the volcano (2 km down to 9-10 km) is a fundamental process controlling magma compositions at Mt. Somma

  5. The effect of secondary apatite on the initial 87Sr/86Sr ratio determination in granitic rocks: a case study of the Tadamigawa pluton, northeastern Japan

    NASA Astrophysics Data System (ADS)

    Wakasugi, Y.; Ichino, K.; Tanioka, Y.; Wakaki, S.; Tsuboi, M.; Ishikawa, T.

    2017-12-01

    Apatite is a major accessory mineral in igneous rocks. Because Rb contents in apatite are very low, 87Sr/86Sr ratios of magmatic apatite are useful to estimate the initial 87Sr/86Sr ratio (SrI) of igneous rocks. Secondary post-magmatic event such as hydrothermal alteration may also crystallize secondary apatite, which may inhibit the estimation of SrI of igneous rocks. In this study, we examine the effects of secondary apatite on the initial 87Sr/86Sr ratio determination of granitic rocks by using acid leaching technique. Leached apatite samples were first separated from the whole rock powder as a heavy mineral fraction by heavy liquid technique, and the heavy mineral fraction was then leached by 3 M HNO3. The isotopic ratios of Sr and the concentrations of Rb and Sr were analyzed by TIMS and ICP-MS at Kochi Core Center, respectively. The Tadamigawa Older-stage granites, which locate in the Taishaku Mountains at the northeastern part of Japan, intrude into the Ashio Jurassic complex, and the ages of these rocks are late Cretaceous to Paleogene. The U-Pb ages of zircon and the K-Ar ages of biotite for these rocks are c. 100 Ma [1, 2]. Rb-Sr whole-rock isochron age of the pluton is 96.5 ± 1.3 Ma (SrI = 0.70534 ± 0.00003) and it is concordant with other radiometric ages. Rb-Sr mineral isochron ages range from 84.4 to 97.3 Ma and these ages are relatively younger than the Rb-Sr whole-rock isochron age. The difference among radiometric ages may reflect the difference of the closure temperature in each isotopic system. The Tadamigawa Older-stage granites have SrI for Rb-Sr mineral isochron range from 0.7053 to 0.7061 and are very similar to that (0.70534) for Rb-Sr whole-rock isochron. These may suggest that the Tadamigawa Older-stage granites are generated from same parental magma. However, 87Sr/86Sr ratios of the leached apatite samples were 0.70544-0.70856 and are relatively higher than SrI obtained from the Rb-Sr mineral isochrons (0.7053-0.7061). This result

  6. The Sr, Nd and O isotopic studies of the 1991 1995 eruption at Unzen, Japan

    NASA Astrophysics Data System (ADS)

    Chen, Chang-Hwa; Nakada, Setsuya; Shieh, Yuch-Ning; DePaolo, Donald J.

    1999-04-01

    The magma generation at Unzen volcano may be considered as the product of crustal material mixed with mantle magma accompanied by fractional crystallization (AFC). The magma in the Unzen volcano is estimated to consist of about 50-80% of residual magma ( F) and about 30-70% assimilated crustal material ( A) relative to the original magma. Concerning the 1991-1995 eruption, it is estimated that the magma formed as the result of mixing of about 50-60% crustal material and about 55-65% of residual magma. An alternative magma eruption model for the 1991-1995 eruption is proposed here. In the early stage, the isotopic characteristics of 1991 eruption are defined by AFC process in the deeper magma chamber. Later, the magma ascended through the conduit and quiescently stayed for a long time in a shallow reservoir before eruption. The minerals continuously crystallized as phenocrysts especially at the chilled top and outer margin in the shallow chamber. The crystallized phenocryst mush was reworked into the central part of the magma chamber by means of magma convection and rapid magma ascent. Therefore, the reaction between phenocrysts and melt occurs only in internal chemical disequilibrium in the magma chamber. In contrast, the isotopic compositions of the original magma shall be little influenced by the above processes throughout its eruptive history. The 1991-1995 eruptive rocks of the Unzen volcano show their characteristics in Sr and Nd isotopic values independent of their two previous eruptions. However, the isotopic values of early eruptive product could represent the original magma value. This result also supports the previous work of Chen et al. (1993) [Chen, C.H., DePaolo, D.J., Nakada, S., Shieh, Y.N., 1993. Relationship between eruption volume and neodymium isotopic composition at Unzen volcano. Nature 362, 831-834], that suggested the ɛNd of early or precursory eruptive products could be a qualitative indicator of the maximum size of a continuing or

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

    NASA Astrophysics Data System (ADS)

    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.

  8. The Strontium Fingerprint and Footprint: Using 87Sr/86Sr to Find the Sources and Range of Architectural Timber Acquisition of Great House Construction at Chaco Canyon, New Mexico

    NASA Astrophysics Data System (ADS)

    English, N. B.; Reynolds, A. C.; Quade, J.; Betancourt, J. L.

    2006-12-01

    We describe the spatial and temporal patterns of timber acquisition by great house builders in Chaco Canyon, New Mexico. The 87Sr/86Sr ratios from annually-dated, architectural logs in 10^{th} to 12^{th} century structures are compared to the 87Sr/86Sr of modern tree stands from the surrounding mountains. Although not a stable isotope system, the long half-life of the 87Sr parent (87Rb, t1/2 = 48.8 Ga) yields a stable isotope system on the timescales used to determine the geographic origin of ecosystem resources. The small mass difference among strontium's isotopes eliminates measurable biologic or kinetic fractionation at earth surface conditions. Strontium tracer studies, however, do require distinct end-member ratios to be feasible. Strontium isotopes, alone or in combination with other isotopes, provide a simple way to study and trace the geographic origin of ecosystem resources. Over the 150 km-wide Chaco Basin, 87Sr/86Sr ratios of modern trees range from 0.7055 to 0.7192. 87Sr/86Sr ratios from this and other studies show that during great house construction Chaco Canyon was provisioned with plant materials that came from more than 75 km away in all directions. This includes (1) corn (Zea mays) grown on the eastern flanks of the Chuska Mountains and floodplain of the San Juan River to the west and north, (2) spruce (Picea sp.) and fir (Abies sp.) architectural beams from the high crests of the Chuska and San Mateo Mountains to the west and south, and (3) ponderosa pine (Pinus ponderosa) from the low slopes of the La Platas and San Juan Mountains to the north, the San Pedro Mountains to the east, the Chuska and San Mateo Mountains and nearby mesas. There are no systematic patterns in spruce/fir or ponderosa provenance by great house (Pueblo Bonito, Chetro Ketl, Pueblo del Arroyo) or by time, suggesting the use of stockpiles from a few preferred sources from the beginning of large scale construction in or around Chaco Canyon. This is contrary to the view that

  9. Oxygen and strontium isotope tracing of human migration at the Bell Beaker site Le Tumulus des Sables, France.

    NASA Astrophysics Data System (ADS)

    Willmes, Malte; James, Hannah; Boel, Ceridwen; Courtaud, Patrice; Chancerel, Antoine; McMorrow, Linda; Armstrong, Richard; Kinsley, Les; Aubert, Maxime; Eggins, Stephen; Moffat, Ian; Grün, Rainer

    2014-05-01

    Oxygen (δ18O) and strontium (87Sr/86Sr) isotopes were used as tools to investigate human migration at the early Bell Beaker site (2500-2000 BC) Le Tumulus des Sables, Saint-Laurent-Médoc, south-west France. The O and Sr isotope ratios measured in tooth enamel record the average dietary isotope signature ingested by that individual during their childhood. When this data is compared to the isotope signature of the burial site it can be used to indicate if the individual migrated into this area during their lifetime. The O isotopic composition of meteoric water changes depending on climate, temperature and quantity of precipitation. O isotope ratios in skeletal and dental remains are related to body water, which in turn is influenced by diet, physiology and climate. Most of the water consumed by large mammals comes from drinking water, typically sourced locally. Sr isotope ratios on the other hand vary between different geologic regions, depending on their age and composition. Sr is released through weathering and transported into the soil, ground and surface water, where it becomes available for uptake by plants, enters the food cycle and eventually ends up in skeletal and dental tissue where it substitutes for calcium. We analysed the teeth of 18 adult and 8 juvenile disarticulated skeletons from Le Tumulus des Sables. O isotopes were analysed in-situ by Sensitive High Resolution Ion Micro Probe (SHRIMP).The Sr isotope analysis involved drilling a 0.2-0.5 mg sample of enamel from the tooth. The Sr was then chemically separated and analysed by Thermal Ionization Mass Spectrometry (TIMS). These results were then compared to the O isoscape of Europe and bioavailable Sr isotope data (fauna, plants, soils) from the IRHUM database. We found that most of the individuals at Le Tumulus des Sables show O and Sr isotope ratios corresponding to the local environmental signal and we interpret these as part of the local population. 3 adults however show slightly higher 87Sr/86

  10. 87Sr/86Sr Across the Devonian-Carboniferous Transition Within the Pho Han Formation, Cat Ba Island, Vietnam: New Data Outside of an Old Orogeny

    NASA Astrophysics Data System (ADS)

    Paschall, O. C.; Carmichael, S. K.; Dombrowski, A. D.; Batchelor, C. J.; Coleman, D. S.; Waters, J. A.; Königshof, P.

    2017-12-01

    The Devonian-Carboniferous (D-C) transition is a period of mass extinction and rapid global faunal changes that affected both marine and terrestrial ecosystems. Although the paleontology and carbon and oxygen isotopes across of the D-C boundary have been studied in detail, there is very little continuous 87Sr/86Sr isotope data for this time iteration due to unconformities and/or diagenetic alteration in many sections. Conodont biostratigraphy indicates that the D-C boundary is present within the Pho Han Formation on Cat Ba Island in northeastern Vietnam. This unit represents a starved basinal facies on the South China carbonate platform, and has continuous sedimentation across the D-C boundary. Whole rock geochemical results indicate increased clastic input at the D-C transition, potentially due to the regression observed in many Hangenberg Event localities around the world, but the isolated nature of the basin could instead indicate complete shutdown of the carbonate factory. New 87Sr/86Sr measurements of carbonate across the D-C boundary in the Pho Han Formation indicate oscillating fluctuations from 0.708052 to 0.708672. Many of these values are within the McArthur et al. (2012) LOWESS fit for seawater, with excursions towards higher values tentatively identified at the boundary between the Palmatolepis expansa and lower Siphonodella praesulcata conodont zones, and within the Siphonodella duplicata zone. There is a lack of correlation between 87Sr/86Sr values with whole rock geochemistry and δ18O isotope values across the section, suggesting that these 87Sr/86Sr values are not due to clastic contamination and that the samples have not experienced major diagenetic alteration. The continuous sedimentation in this section and its location in an area far from the Variscan orogeny make this unit a valuable site in which to compare 87Sr/86Sr ratios to existing studies in Europe and North America which experienced substantial sediment shedding from the Appalachian

  11. Fluid/rock Interaction History of a Faulted Rhyolite-Granite Contact Determined by Sr- Pb-Isotopes, Th/U-Disequilibria and Elemental Distributions (Eastern Rhine Graben Shoulder, SW-Germany)

    NASA Astrophysics Data System (ADS)

    Marbach, T.; Mangini, A.; Kober, B.; Schleicher, A.; Warr, L. N.

    2003-04-01

    Major and trace element analyses allow to obtain information concerning the chemical changes induced by alteration. Differences are partly petrographic because the profile crosses the granite-rhyolite contact, but they are also due to different alteration levels induced by fluid circulation along the fault system which has drained the alteration processes. The granite-rhyolite contact constitutes the primary structure. Only the most incompatible elements (Si, Al, Zr, Hf) retain their original signatures and reflect a mixing between typical granite and rhyolite lithologies across the altered zones (cataclasite). The more mobile elements show a different composition within the altered zones (cataclasite) notably a high leaching of cations. The geochemical tracers also suggest at least one strong hydrothermal event with reducing conditions in the altered zones. The isotopic analyses delivered qualitative and temporal information. The use of several isotopic systems, Rb/Sr-, U/Pb-isotopes and Th/U disequilibria, reveals a complex history of polyphase fluid/rock interaction following the Permian volcanic extrusion, showing notable disturbances during the late Jurassic hydrothermal activities, the Tertiary rifting of the Rhine Graben and more recent Quaternary alteration. The granite zone of the sampling profile has underwent an event which set up a new Rb-Sr isotopic composition and reset the Rb/Sr system which originatly corresponded to the Carboniferous intrusion ages. The Rb-Sr data of the granite samples produce a whole rock isochron of 152 ± 5,7 Ma (2σ error) in good agreement with the well-known late Jurassic hydrothermal event (135--160 Ma). The rocks evolution lines for Pb support a Tertiary hydrothermal event (54 Ma ± 16; 1σ error), potentially connected with the development of the Rhine Graben. The profile samples have undergone uranium and thorium redistribution processes which have occurred within the last ˜10^6 years. The samples of the altered zones

  12. Anthropogenic versus natural control on trace element and Sr-Nd-Pb isotope stratigraphy in peat sediments of southeast Florida (USA), ˜1500 AD to present

    NASA Astrophysics Data System (ADS)

    Kamenov, George D.; Brenner, Mark; Tucker, Jaimie L.

    2009-06-01

    is oil combustion. The decline in V accumulation after 1970 in the BCM peat corresponds to the introduction of low-sulfur fuels and the change from heavy to distilled oils since the 1970s. After the 1920s, Pb distribution in the peat follows closely the history of alkyl lead consumption in the US, which peaked in the 1970s. Pb isotopes support this inference and furthermore, record changes in the ore sources used to produce leaded gasoline. Idaho ores dominated the peat Pb isotope record until the 1960s, followed by Pb from Mississippi Valley Type deposits from the 1960s to the 1980s. Enhanced fluxes of Cu, Zn, Cd, Sn, Sb, Bi, and to some extent Ni during the last century are likely also related to fossil fuel combustion. Local agricultural activities may also have influenced the geochemical cycles of Cu and Zn. The peat record shows enhanced U accumulation during the last century, possibly related to phosphate mining in western Florida. Sr isotopes in the peat core also reflect anthropogenic influence. The 87Sr/ 86Sr ratio decreases from natural background values in the basal part of the core to lower values in the upper part of the core. The Sr isotope shift is probably related to quarrying operations in Florida, and marks the first time an anthropogenic signal has been detected using the Sr isotope record in a peat core.

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

    NASA Astrophysics Data System (ADS)

    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. Across-arc versus along-arc Sr-Nd-Pb isotope variations in the Ecuadorian volcanic arc

    NASA Astrophysics Data System (ADS)

    Ancellin, Marie-Anne; Samaniego, Pablo; Vlastélic, Ivan; Nauret, François; Gannoun, Adbelmouhcine; Hidalgo, Silvana

    2017-03-01

    Previous studies of the Ecuadorian arc (1°N-2°S) have revealed across-arc geochemical trends that are consistent with a decrease in mantle melting and slab dehydration away from the trench. The aim of this work is to evaluate how these processes vary along the arc in response to small-scale changes in the age of the subducted plate, subduction angle, and continental crustal basement. We use an extensive database of 1437 samples containing 71 new analyses, of major and trace elements as well as Sr-Nd-Pb isotopes from Ecuadorian and South Colombian volcanic centers. Large geochemical variations are found to occur along the Ecuadorian arc, in particular along the front arc, which encompasses 99% and 71% of the total variations in 206Pb/204Pb and 87Sr/86Sr ratios of Quaternary Ecuadorian volcanics, respectively. The front arc volcanoes also show two major latitudinal trends: (1) the southward increase of 207Pb/204Pb and decrease of 143Nd/144Nd reflect more extensive crustal contamination of magma in the southern part (up to 14%); and (2) the increase of 206Pb/204Pb and decrease of Ba/Th away from ˜0.5°S result from the changing nature of metasomatism in the subarc mantle wedge with the aqueous fluid/siliceous slab melt ratio decreasing away from 0.5°S. Subduction of a younger and warmer oceanic crust in the Northern part of the arc might promote slab melting. Conversely, the subduction of a colder oceanic crust south of the Grijalva Fracture Zone and higher crustal assimilation lead to the reduction of slab contribution in southern part of the arc.

  15. Major and trace element, and Sr isotope compositions of clinopyroxene phenocrysts in mafic dykes on Jiaodong Peninsula, southeastern North China Craton: Insights into magma mixing and source metasomatism

    NASA Astrophysics Data System (ADS)

    Liang, Yayun; Deng, Jun; Liu, Xuefei; Wang, Qingfei; Qin, Cheng; Li, Yan; Yang, Yi; Zhou, Mian; Jiang, Jieyan

    2018-03-01

    Early Cretaceous mafic dyke swarms are widely developed on Jiaodong Peninsula in the southeastern part of the North China Craton (NCC), but their petrogenesis remains enigmatic. We have examined the in-situ major element, trace element and Sr isotope compositions of the clinopyroxene phenocrysts in these dykes in order to evaluate the extent of magma mixing and source metasomatism. Depending on the type of mineral zoning, the clinopyroxene phenocrysts in our samples can be classified into two groups: Group I (reverse zoning) and Group II (no zoning). Based on core compositions, the Group I phenocrysts with obvious reverse zoning can be divided into two subgroups: Groups IA and IB. The cores of Group IA clinopyroxenes have low values of Mg#, low Al2O3 contents, high Na2O contents, and high 87Sr/86Sr ratios, and they were probably derived from newly accreted lower crust that formed through the underplating of basaltic magma. In contrast, the cores of Group IB clinopyroxenes have lower Mg# values and lower contents of Al2O3, ΣREE (total rare earth elements), and incompatible elements, but they have similar 87Sr/86Sr ratios; these cores crystallised from crust-derived andesitic-dacitic magma. Group IA and IB clinopyroxene phenocryst rims (Group I rims) all have similar compositions with higher values of Mg# and higher Al2O3, Cr and Ni contents than the cores. The rims have high 87Sr/86Sr ratios, are enriched in LREEs (light rare earth elements) and LILEs (large ion lithophile elements), and are depleted in HFSEs (high field strength elements); these characteristics indicate that all the high-Mg rims were derived from a similar magma, possibly a relatively primitive magma derived from lithospheric mantle. We suggest, therefore, that the reversely-zoned clinopyroxene phenocrysts (Group I) in the Jiaodong mafic dykes provide evidence of magma mixing between a magma derived from lithospheric mantle and crust-derived andesitic-dacitic melt alongside with the newly accreted

  16. Isotopically distinct reservoirs in the solar nebula: Isotope anomalies in Vigarano meteorite inclusions

    NASA Technical Reports Server (NTRS)

    Loss, R. D.; Lugmair, G. W.; Davis, A. M.; Macpherson, G. J.

    1994-01-01

    The isotopic compositions of Mg, Ca, Ti, Cr, Zn, Sr, Ba, Nd, and Sm were measured in four relatively unaltered refractory inclusions from the Vigarano carbonaceous chondrite meteorite. Three of the inclusions (USNM 1623-2, 1623-3, and 1623-8) show similar Mg, Ca, Ti, and Cr isotopic compositions to those found in most inclusions in the Allende carbonaceous chondrite. This indicates that these Vigarano inclusions sampled the same isotopic reservoirs as the majority of the Allende inclusions that isotope signatures in the latter were not significantly modified by the secondary alteration that permeates most Allende inclusions. In contrast, inclusion 1623-5 has large deficits in Mg-26, Ca-48, and Ti-50 and small but distinct Cr-54, Zn-66, Sr-84, Ba-135, Ba-137, and Sm-144 anomalies. The magnitudes of these unusual anomalies in the refractory elements are within analytical uncertainty of those found in the Allende 'FUN" inclusion C1, yet 1623-5 has a very different bulk chemical composition from C1. The fact that 1623-5 and C1 have identical isotopic anomalies yet have significantly distinct major and trace element contents provide convincing evidence for the presence of isotopically distinct reservoirs in the early solar system.

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

    PubMed

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

    2017-02-15

    The increasing demand for premium priced Indian Basmati rice (Oryza sativa) in world commodity market causing fraudulent activities like adulteration, mislabelling. In order to develop authentication method for Indian Basmati rice, (87)Sr/(86)Sr ratios and REEs composition of Basmati rice, soil and water samples were determined and evaluated their ability as geographical tracer in the present study. In addition, the possible source of Sr in rice plant has also been examined. Basmati rice samples (n=82) showed (87)Sr/(86)Sr ratios in the range 0.71143-0.73448 and concentrations of 10 REEs (La, Ce, Pr, Nd, Sm, Eu, Gd, Dy, Er, Yb) in ppb levels. Statistical analysis showed strong correlation between (87)Sr/(86)Sr ratios of rice, silicate and carbonate fractions of soil. Good correlation and closeness of (87)Sr/(86)Sr of rice with water indicate its uptake in rice from water. Rice grown in southern Uttar Pradesh contains higher (87)Sr/(86)Sr compared to other region of Indo-Gangetic Plain due to higher (87)Sr/(86)Sr of the Ganga compared to other rivers. (87)Sr/(86)Sr ratios can be used as a tracer for differentiating Indian Basmati rice from the other country originated rice samples. Copyright © 2016 Elsevier Ltd. All rights reserved.

  18. A Rb-Sr and Sm-Nd Isotope Geochronology and Trace Element Study of Lunar Meteorite LaPaz Icefield 02205

    NASA Technical Reports Server (NTRS)

    Rankenburg, K.; Brandon, A. D.; Norman, M. D.

    2007-01-01

    Rubidium-strontium and samarium-neodymium isotopes of lunar meteorite LaPaz Icefield (LAP) 02205 are consistent with derivation of the parent magma from a source region similar to that which produced the Apollo 12 low-Ti olivine basalts followed by mixing of the magma with small amounts (1 to 2 wt%) of trace element-enriched material similar to lunar KREEP-rich sample SaU 169. The crystallization age of LAP 02205 is most precisely dated by an internal Rb-Sr isochron of 2991+/-14 Ma, with an initial Sr-87/Sr-88 at the time of crystallization of 0.699836+/-0.000010. Leachable REE-rich phosphate phases of LAP 02205 do not plot on a Sm-Nd mineral isochron, indicating contamination or open system behavior of the phosphates. Excluding anomalous phases from the calculation of a Sm-Nd isochron yields a crystallization age of 2992+/-85 (initial Epsilon Nd-143 = +2.9+/-0.8) that is within error of the Rb-Sr age, and in agreement with other independent age determinations for LAP 02205 from Ar-Ar and U-Pb methods. The calculated Sm-147/Nd-144 source ratios for LAP 02205, various Apollo 12 and 15 basalts, and samples with strong affinities to KREEP (SaU 169, NWA 773, 15386) are uncorrelated with their crystallization ages. This finding does not support the involvement of a common KREEP component as a heat source for lunar melting events that occurred after crystallization of the lunar magma ocean.

  19. Hafnium isotope results from mid-ocean ridges and Kerguelen

    USGS Publications Warehouse

    Jonathan, Patchett P.

    1983-01-01

    176Hf/177Hf ratios are presented for oceanic volcanics representing both extremes of the range of mantle HfNdSr isotopic variation. Hf from critical mid-ocean ridgebasalts shows that 176Hf/177Hf does indeed have a greater variability than 143Nd/144Nd and 87Sr/86Sr in the depleted mantle. This extra variation is essentially of a random nature, and can perhaps be understood in terms of known Rb/SrSm/NdLu/Hf fractionation relationships. At the other extreme of mantle isotopic composition, 176Hf/177Hf ratios for igneous rocks from the Indian Ocean island of Kerguelen show a closely similar variation to published 143Nd/144Nd ratios for the same samples. Comparison of HfNdSr c relationships for Tristan da Cunha, Kerguelen and Samoa reveals divergences in the mantle array for ocean island magma sources, and perhaps suggests that these irregularities are largely the result of an extra component of 87Sr/86Sr variation. ?? 1983.

  20. 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

    NASA Astrophysics Data System (ADS)

    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

  1. Rb-Sr and Sm-Nd Isotopic Studies of Antarctic Nakhlite MIL 03346

    NASA Technical Reports Server (NTRS)

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

    2006-01-01

    Nakhlites are olivine-bearing clinopyroxenites with cumulate textures, and probably came from Mars [e.g., 1]. A total of seven nakhlites have been identified so far. Unlike other martian meteorites (e.g., shergottites), nakhlites have been only moderately shocked and their original igneous textures are still well-preserved. Also, these meteorites have similarly older crystallization ages of approx.1.3 Ga compared to shergottites with ages of approx.0.18-0.57 Ga [e.g., 2]. MIL 03346 is characterized by abundant (approx.20 vol %) glassy mesostasis, indicating that it cooled rapidly and probably formed near the top [3] or at the bottom [4] of the chilled margin of a thick intrusive body. The mesostasis quenched from the trapped intercumulus liquid may provide information on the parent magma compositions of the nakhlites. In this report, we present Rb-Sr and Sm-Nd isotopic data for MIL 03346, discuss correlation of its age with those of other nakhlites and the nature of their source regions in the Martian mantle.

  2. Reconstructing geochemical conditions during dolomite formation in a Carnian coastal sabkha using 87Sr/86Sr isotopes - Travenanzes Formation, northern Italy

    NASA Astrophysics Data System (ADS)

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

    2017-04-01

    The geochemical conditions that were conducive to primary dolomite formation in extremely shallow evaporitic environments along the Triassic Tethyan margin are still poorly understood. While the massive Triassic dolomites in the Austroalpine and South Alpine realm are largely affected by diagenetic or hydrothermal overprint, Preto et al. (2015) provide evidence of primary dolomite based on nano-crystal aggregates observed under the transmission electron microscope. These dolomites are intercalated in a 100-m-thick sequence of clay (Travenanzes Formation, Southern Alps), deposited on a semi-arid coastal plain in the Late Carnian (Tuvalian II). They may serve as a geochemical archive of evaporative brine composition at the time of dolomite formation. Petrographic and field observations revealed that dolomites occur as three different types, (1) dm- to m-thick homogenous beds, (2) mm-scale laminated (stromatolitic) beds and (3) nodules associated with root traces and palaeosols. In all types, the dolomite is stoichiometrically and structurally well ordered. While the homogeneous dolomites occasionally show a peloidal structure, all types of dolomite are generally microcrystalline. Soft sediment deformation, or brittle deformation with mud infill indicates that the dolomitic sediment was largely unlithified at the time of deposition. We analysed the dolomites under the SEM in backscatter mode and observed largely anhedral structures with grain sizes in the μm-range. The laminated dolomites consist of mm- to cm-scale clay-dolomite alternations, whereby the dolomite often shows a spherulitic growth near the dolomite-clay interface, where further recrystallization was inhibited. We measured strontium isotope ratios (87Sr/86Sr) as an indicator for the source of alkalinity driving dolomite precipitation. Our data are in a range between 0.707672 (homogenous dolomite) and 0.707976 (both 2σ: 4*10-5) (nodular dolomite) indicating a similar trend as in Triassic seawater during

  3. Neodymium and strontium isotopic dating of diagenesis and low-grade metamorphism of argillaceous sediments

    NASA Astrophysics Data System (ADS)

    Schaltegger, Urs; Stille, Peter; Rais, Naoual; Piqué, Alain; Clauer, Norbert

    1994-03-01

    The behaviour of the Rb-Sr and Sm-Nd isotopic systems with increasing degree of Hercynian metamorphic overprint was studied along a transect in Cambrian shales of northwestern Morocco. Clay fractions of < 0.2 to 2-6 μm size from five samples were investigated, representing a range from nonmetamorphic to epizonal metamorphic conditions. The samples were washed in cold l N HC1 prior to digestion to separate soluble/exchangeable Rb, Sr, Sm, and Nd from amounts of these elements fixed in the crystallographic sites of the minerals and to analyze both components separately. The results reveal that the Rb-Sr isotopic system is dominated by Sr hosted by clay mineral phases (both detrital and authigenic illite and chlorite) and carbonate-hosted soluble Sr. Isotopic homogenization of Sr occurred during Hercynian metamorphism, yielding ages between 309 and 349 Ma. The Sm-Nd isotopic system, on the other hand, is dominated by cogenetic apatite and Fe oxide/ hydroxide, both having high contents of leachable REEs. The leachates yield a Sm-Nd isochron age of 523 ± 72 Ma, indicating diagenetic equilibrium between apatite and Fe-oxide/hydroxide. Fine-grained clay fractions of < 0.2 μm size plot onto this reference line, suggesting isotopic equilibrium with the leachates. Size fractions > 0.2 μm show inheritance of a detrital Nd component. The study demonstrates that the diagenesis of the investigated argillaceous sediments can be dated by the Sm-Nd chronometer in authigenic cement phases. The isotopic system of these minerals (apatite, Fe hydroxide/oxide) was homogenized during authigenic mineral growth in a sediment that was flushed by diagenetic fluids and had abundant primary or secondary interconnected pore space. The Hercynian metamorphic overprint caused partial isotopic rehomogenization of the adsorbed and clay-hosted portion of the Sr as well as of the carbonate-hosted Sr. The Sm-Nd system in the cement phases survived this metamorphism. This results in decoupling of

  4. Ca cycling and isotopic fluxes in forested ecosystems in Hawaii

    USGS Publications Warehouse

    Wiegand, B.A.; Chadwick, O.A.; Vitousek, P.M.; Wooden, J.L.

    2005-01-01

    Biogeochemical processes fractionate Ca isotopes in plants and soils along a 4 million year developmental sequence in the Hawaiian Islands. We observed that plants preferentially take up 40Ca relative to 44Ca, and that biological fractionation and changes in the relative contributions from volcanic and marine sources produce a significant increase in 44Ca in soil exchangeable pools. Our results imply moderate fluxes enriched in 44Ca from strongly nutrient-depleted old soils, in contrast with high 40Ca fluxes in young and little weathered environments. In addition, biological fractionation controls divergent geochemical pathways of Ca and Sr in the plant-soil system. While Ca depletes progressively with increasing soil age, Sr/Ca ratios increase systematically. Sr isotope ratios provide a valuable tracer for provenance studies of alkaline earth elements in forested ecosystems, but its usefulness is limited when deciphering biogeochemical processes involved in the terrestrial Ca cycle. Ca isotopes in combination with Sr/ Ca ratios reveal more complex processes involved in the biogeochemistry of Ca and Sr. Copyright 2005 by the American Geophysical Union.

  5. Using noble gases and 87Sr/86Sr to constrain heat sources and fluid evolution at the Los Azufres Geothermal Field, Mexico

    NASA Astrophysics Data System (ADS)

    Wen, T.; Pinti, D. L.; Castro, M. C.; Lopez Hernandez, A.; Hall, C. M.; Shouakar-Stash, O.; Sandoval-Medina, F.

    2017-12-01

    Geothermal wells and hot springs were sampled for noble gases' volume fraction and isotopic measurements and 87Sr/86Sr in the Los Azufres Geothermal Field (LAGF), Mexico, to understand the evolution of fluid circulation following three decades of exploitation and re-injection of used brines. The LAGF, divided into the Southern Production Zone (SPZ) and the Northern Production Zone (NPZ), is hosted in a Miocene to Pliocene andesitic volcanic complex covered by Quaternary rhyolitic-dacitic units. Air contamination corrected 3He/4He ratios (Rc) normalized to the atmospheric ratio (Ra=1.384 x 10-6), show a median value of 6.58 indicating a dominant mantle helium component. Contributions of crustal helium up to 53% and 18% are observed in NPZ and SPZ, respectively. Observations based on Rc/Ra and 87Sr/86Sr ratios points to the mixing of three magmatic sources supplying mantle helium to the LAGF: (1) a pure mantle He (Rc/Ra = 8) and Sr (87Sr/86Sr = 0.7035) source; (2) a pure mantle helium (Rc/Ra = 8) with some radiogenic Sr (87Sr/86Sr = 0.7049) source possibly resulting from Quaternary rhyolitic volcanism; and (3) a fossil mantle He component (Rc/Ra = 3.8) with some radiogenic Sr (87Sr/86Sr = 0.7038), corresponding possibly to the Miocene andesite reservoir. Intrusions within the last 50 kyrs from sources (1) and (2) are likely responsible for the addition of mantle volatiles and heat to the hydrothermal system of Los Azufres. He and Ar isotopes indicate that heat flow is transported by both convection and conduction. Atmospheric noble gas elemental ratios suggest that geothermal wells located closer to the western re-injection zone are beginning to be dominated by re-injection of used brines (injectate). The area affected by boiling in LAGF has further extended to the north and west since the last noble gas sampling campaign in 2009.

  6. 87Sr/86Sr sourcing of ponderosa pine used in Anasazi great house construction at Chaco Canyon, New Mexico

    USGS Publications Warehouse

    Reynolds, Amanda C.; Betancourt, Julio L.; Quade, Jay; Patchett, P. Jonathan; Dean, Jeffery S.; Stein, John

    2005-01-01

    Previous analysis of 87Sr/86Sr ratios shows that 10th through 12th century Chaco Canyon was provisioned with plant materials that came from more than 75 km away. This includes (1) corn (Zea mays) grown on the eastern flanks of the Chuska Mountains and floodplain of the San Juan River to the west and north, and (2) spruce (Picea sp.) and fir (Abies sp.) beams from the crest of the Chuska and San Mateo Mountains to the west and south. Here, we extend 87Sr/86Sr analysis to ponderosa pine (Pinus ponderosa) prevalent in the architectural timber at three of the Chacoan great houses (Pueblo Bonito, Chetro Ketl, Pueblo del Arroyo). Like the architectural spruce and fir, much of the ponderosa matches the 87Sr/86Sr ratios of living trees in the Chuska Mountains. Many of the architectural ponderosa, however, have similar ratios to living trees in the La Plata and San Juan Mountains to the north and Lobo Mesa/Hosta Butte to the south. There are no systematic patterns in spruce/fir or ponderosa provenance by great house or time, suggesting the use of stockpiles from a few preferred sources. The multiple and distant sources for food and timber, now based on hundreds of isotopic values from modern and archeological samples, confirm conventional wisdom about the geographic scope of the larger Chacoan system. The complexity of this procurement warns against simple generalizations based on just one species, a single class of botanical artifact, or a few isotopic values.

  7. 87Sr/86Sr sourcing of ponderosa pine used in Anasazi great house construction at Chaco Canyon, New Mexico

    USGS Publications Warehouse

    Reynolds, A.C.; Betancourt, J.L.; Quade, Jay; Patchett, P.J.; Dean, J.S.; Stein, J.

    2005-01-01

    Previous analysis of 87Sr/86Sr ratios shows that 10th through 12th century Chaco Canyon was provisioned with plant materials that came from more than 75 km away. This includes (1) corn (Zea mays) grown on the eastern flanks of the Chuska Mountains and floodplain of the San Juan River to the west and north, and (2) spruce (Picea sp.) and fir (Abies sp.) beams from the crest of the Chuska and San Mateo Mountains to the west and south. Here, we extend 87Sr/86Sr analysis to ponderosa pine (Pinus ponderosa) prevalent in the architectural timber at three of the Chacoan great houses (Pueblo Bonito, Chetro Ketl, Pueblo del Arroyo). Like the architectural spruce and fir, much of the ponderosa matches the 87Sr/86Sr ratios of living trees in the Chuska Mountains. Many of the architectural ponderosa, however, have similar ratios to living trees in the La Plata and San Juan Mountains to the north and Lobo Mesa/Hosta Butte to the south. There are no systematic patterns in spruce/fir or ponderosa provenance by great house or time, suggesting the use of stockpiles from a few preferred sources. The multiple and distant sources for food and timber, now based on hundreds of isotopic values from modern and archeological samples, confirm conventional wisdom about the geographic scope of the larger Chacoan system. The complexity of this procurement warns against simple generalizations based on just one species, a single class of botanical artifact, or a few isotopic values. ?? 2005 Elsevier Ltd. All rights reserved.

  8. pH-Dependent isotope exchange and hydrogenation catalysed by water-soluble NiRu complexes as functional models for [NiFe]hydrogenases.

    PubMed

    Kure, Bunsho; Matsumoto, Takahiro; Ichikawa, Koji; Fukuzumi, Shunichi; Higuchi, Yoshiki; Yagi, Tatsuhiko; Ogo, Seiji

    2008-09-21

    The pH-dependent hydrogen isotope exchange reaction between gaseous isotopes and medium isotopes and hydrogenation of the carbonyl compounds have been investigated with water-soluble bis(mu-thiolate)(mu-hydride)NiRu complexes, Ni(II)(mu-SR)(2)(mu-H)Ru(II) {(mu-SR)(2) = N,N'-dimethyl-N,N'-bis(2-mercaptoethyl)-1,3-propanediamine}, as functional models for [NiFe]hydrogenases. In acidic media (at pH 4-6), the mu-H ligand of the Ni(II)(mu-SR)(2)(mu-H)Ru(II) complexes has H(+) properties, and the complexes catalyse the hydrogen isotope exchange reaction between gaseous isotopes and medium isotopes. A mechanism of the hydrogen isotope exchange reaction between gaseous isotopes and medium isotopes through a low-valent Ni(I)(mu-SR)(2)Ru(I) complex is proposed. In contrast, in neutral-basic media (at pH 7-10), the mu-H ligand of the Ni(II)(mu-SR)(2)(mu-H)Ru(II) complexes acts as H(-), and the complexes catalyse the hydrogenation of carbonyl compounds.

  9. Cenozoic seawater Sr/Ca evolution

    NASA Astrophysics Data System (ADS)

    Sosdian, Sindia M.; Lear, Caroline H.; Tao, Kai; Grossman, Ethan L.; O'Dea, Aaron; Rosenthal, Yair

    2012-10-01

    Records of seawater chemistry help constrain temporal variations in geochemical processes that impact the global carbon cycle and climate through Earth's history. Here we reconstruct Cenozoic seawater Sr/Ca (Sr/Casw) using fossil Conus and turritellid gastropod Sr/Ca. Combined with an oxygen isotope paleotemperature record from the same samples, the gastropod record suggests that Sr/Caswwas slightly higher in the Eocene (˜11.4 ± 3 mmol/mol) than today (˜8.54 mmol/mol) and remained relatively stable from the mid- to late Cenozoic. We compare our gastropod Cenozoic Sr/Casw record with a published turritellid gastropod Sr/Casw record and other published biogenic (benthic foraminifera, fossil fish teeth) and inorganic precipitate (calcite veins) Sr/Caswrecords. Once the uncertainties with our gastropod-derived Sr/Casw are taken into account the Sr/Casw record agrees reasonably well with biogenic Sr/Caswrecords. Assuming a seawater [Ca] history derived from marine evaporite inclusions, all biogenic-based Sr/Casw reconstructions imply decreasing seawater [Sr] through the Cenozoic, whereas the calcite vein Sr/Casw reconstruction implies increasing [Sr] through the Cenozoic. We apply a simple geochemical model to examine the implications of divergence among these seawater [Sr] reconstructions and suggest that the interpretation and uncertainties associated with the gastropod and calcite vein proxies need to be revisited. Used in conjunction with records of carbonate depositional fluxes, our favored seawater Sr/Ca scenarios point to a significant increase in the proportion of aragonite versus calcite deposition in shelf sediments from the Middle Miocene, coincident with the proliferation of coral reefs. We propose that this occurred at least 10 million years after the seawater Mg/Ca threshold was passed, and was instead aided by declining levels of atmospheric carbon dioxide.

  10. Isotopic composition of Pb and Th in interplinian volcanics from Somma-Vesuvius volcano, Italy

    USGS Publications Warehouse

    Cortini, M.; Ayuso, R.A.; de Vivo, B.; Holden, P.; Somma, R.

    2004-01-01

    We present a detailed isotopic study of volcanic rocks emitted from Somma-Vesuvius volcano during three periods of interplinian activity: "Protohistoric" (3550 y B.P. to 79 A.D.), "Ancient Historic" (79 to 472 A.D.) and "Medieval" (472 to 1631 A.D.). Pb isotopic compositions of two acid leached fractions and whole rock residues of 37 whole rock samples (determined by Somma et al., 2001) show that each of the three interplinian periods is distinguished by small, systematic, and unique uranogenic and thorogenic Pb isotopic trends. This key and novel feature is compatible with the notion that the Pb isotopic data reflect small-scale source heterogeneity operating over relatively short periods of time. From this representative group of samples, a selected set of nine whole rocks were analysed for Th isotopes. 232Th/238U ratios in the source can be obtained independently from Pb and from Th isotopes. Those obtained from Pb isotopes represent source ratios, time-integrated over the whole age of the Earth; they range from 3.9 to 4.1. 232Th/238U obtained from Th isotopes are those of the present source. They are lower, and cluster around 3.5; this difference probably indicates recent U enrichment of the present source. The behaviour of Pb, as inferred by its isotopic ratios, is quite distinct from that of Sr and Nd isotopes: Pb isotope variations are not correlated to Sr or Nd isotope variations. The isotopic contrast is compatible with the idea that the isotopes were decoupled during magmatic production, evolution, and ascent through the crust. Thus, the Pb isotopes do not reflect the effects of the same processes as in the case of the Sr and Nd isotopes, or, as we also favor, they do not necessarily reflect the same source contributions into the magmas. Moreover, the Pb isotopic evolution of the interplinian rocks chiefly reflects mixing, driven by processes that are superimposed on, and independent of, other source contributions that determine the isotopic compositions

  11. Stable isotope analysis of Dacryoconarid carbonate microfossils: a new tool for Devonian oxygen and carbon isotope stratigraphy.

    PubMed

    Frappier, Amy Benoit; Lindemann, Richard H; Frappier, Brian R

    2015-04-30

    warrant further exploration of dacryoconarid stable isotope proxy sensitivity, the isotopic contrast among dacryoconarids, other taxa, and bulk rock, as well as other potential dacryoconarid proxies (Mg/Ca, Sr/Ca, (87) Sr/(86) Sr, microlaser and ion microprobe isotope techniques, and clumped isotopes) for stratigraphic research. Copyright © 2015 John Wiley & Sons, Ltd.

  12. Pb-Sr isotopic and geochemical constraints on sources and processes of lead contamination in well waters and soil from former fruit orchards, Pennsylvania, USA: A legacy of anthropogenic activities

    USGS Publications Warehouse

    Ayuso, Robert A.; Foley, Nora K.

    2016-01-01

    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, PA, were evaluated to discern anthropogenic from geogenic sources. Pb (n = 144) and Sr (n = 40) isotopic data and REE (n = 29) 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 (n = 94), together with locally used Pb-As pesticide (n = 5). Waters from residential and test wells show overlapping values of 206Pb/207Pb, 208Pb/207Pb and 87Sr/86Sr. Larger negative Ce anomalies (Ce/Ce*) distinguish residential wells from test wells. Results show that residential and test well waters, sediments from residential water filters in water tanks, and surface waters display broad linear trends in Pb isotope plots. Pb isotope data for soils, bedrock, and pesticides have contrasting ranges and overlapping trends. Contributions of Pb from soils to residential well waters are limited and implicated primarily in wells having shallow water-bearing zones and carrying high sediment contents. 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 sediment build up in residential water tanks. Redox reactions, triggered by influx of groundwater via wells into the residential water systems and leading to subtle changes in pH, are implicated in precipitation of Fe oxyhydroxides

  13. Determining Solute Sources and Water Flowpaths in a Forested Headwater Catchment: Advances With the Ca-Sr-Ba Multi-tracer

    NASA Astrophysics Data System (ADS)

    Bullen, T. D.; Bailey, S. W.; McGuire, K. J.; Zimmer, M. A.; Ross, D. S.

    2011-12-01

    Determining solute sources and water flowpaths in catchments is of critical importance to development of models that effectively describe catchment function. For solutes in soil water and stream water, simple mass balance models that compare precipitation input to catchment outlet compositions can predict average mineral weathering contributions for the catchment as a whole, but fail to provide information about either variability of contributions from different portions of the catchment and different soil depths or processes such as ion exchange and biological cycling. In order to better understand how forested headwater catchments function, we are interpreting concentration and isotope ratios of the alkaline earth elements Ca, Sr and Ba in streamwater, groundwater, the soil ion exchange pool and plants in a hydropedologic context at the 41 hectare hydrologic reference catchment (Watershed 3) at the Hubbard Brook Experimental Forest, New Hampshire, USA. This forested headwater catchment consists of a beech-birch-maple-spruce forest growing on vertically- and laterally-developed Spodosols and Inceptisols formed on granitoid glacial till that mantles Paleozoic metamorphic bedrock. Across the watershed in terms of the soil ion exchange pool, the forest floor has high Sr/Ba and Ca/Sr ratios, mineral soils have intermediate Sr/Ba and low Ca/Sr, and relatively unweathered till in the C horizon has low Sr/Ba and high Ca/Sr. Waters moving through these various compartments will obtain Sr/Ba and Ca/Sr ratios reflecting these characteristics, and thus variations of Sr/Ba and Ca/Sr of streamwater provide evidence of the depth of water flowpaths feeding the streams. 87Sr/86Sr of exchangeable Sr spans a broad range from 0.715 to 0.725, with highest values along the mid-to upper flanks of the catchment and lowest values in a broad zone along the central axis of the catchment associated with numerous groundwater seeps. Thus, variations of 87Sr/86Sr in streamwater provide

  14. Isotopes as Tracers of the Hawaiian Coffee-Producing Regions

    PubMed Central

    2011-01-01

    Green coffee bean isotopes have been used to trace the effects of different climatic and geological characteristics associated with the Hawaii islands. Isotope ratio mass spectrometry (IRMS) and inductively coupled plasma mass spectrometry ((MC)-ICP-SFMS and ICP-QMS) were applied to determine the isotopic composition of carbon (δ13C), nitrogen (δ15N), sulfur (δ34S), and oxygen (δ18O), the isotope abundance of strontium (87Sr/86Sr), and the concentrations of 30 different elements in 47 green coffees. The coffees were produced in five Hawaii regions: Hawaii, Kauai, Maui, Molokai, and Oahu. Results indicate that coffee plant seed isotopes reflect interactions between the coffee plant and the local environment. Accordingly, the obtained analytical fingerprinting could be used to discriminate between the different Hawaii regions studied. PMID:21838232

  15. Extreme isotopic variations in the upper mantle: evidence from Ronda

    NASA Astrophysics Data System (ADS)

    Reisberg, Laurie; Zindler, Alan

    1986-12-01

    The Ronda Ultramafic Complex in southern Spain represents a piece of the Earth's mantle which has been tectonically emplaced into the crust. Nd and Sr isotopic analyses are presented for leached, hand-picked Cr-diopside separates prepared from 15 rock and 18 river sediment samples from Ronda. These results demonstrate that within this small, contiguous body there exists the entire range of Nd isotopic compositions, and much of the range of Sr compositions, found in rocks derived from the sub-oceanic mantle. The sediment cpx samples show that the average isotopic composition of the massif becomes progressively less "depleted" moving from SW to NE along the long axis of the massif. The rock cpx samples document 143Nd/ 144Nd variations from 0.5129 to 0.5126 and 87Sr/ 86Sr variations from 0.7031 to 0.7039 within a uniform outcrop less than 10 m in extent. Thus, extreme isotopic fluctuations exist over a wide range of wavelengths. Sr and Nd isotopes are generally inversely correlated, forming a trend on a Nd-Sr diagram that sharply crosscuts that of the "mantle array". Many of the 143Nd/ 144Nd values, and all of the Sm/Nd values, from one section of the massif are lower than that SCV015SCV0 of the bulk earth, implying that this region existed, or was influenced by a component which existed, in a LREE-enriched environment for a significant period of time. Among the sediment cpxs there is a positive correlation between 143Nd/ 144Nd and 147Sm/ 144Nd. The rock cpx separates display considerably more scatter. A simple, single-stage differentiation event starting with a uniform mantle source cannot explain these results. At least one episode of mixing with a LREE-enriched component is required. If these results from Ronda are typical of the upper mantle, basalts with different isotopic compositions need not derive from spatially separated mantle sources.

  16. Pb, Sr and Nd isotopic composition and trace element characteristics of coarse airborne particles collected with passive samplers

    NASA Astrophysics Data System (ADS)

    Hoàng-Hòa, Thi Bich; Stille, Peter; Dietze, Volker; Guéguen, Florence; Perrone, Thierry; Gieré, Reto

    2015-09-01

    Passive samplers for collection of coarse airborne particulate matter have been installed in and around the coal-mining town of Cam Pha, Quang Ninh Province (Vietnam). Analysis of Pb, Sr, and Nd isotope ratios and of major and trace element distribution patterns in atmospheric particulates collected at three stations allowed for the identification of four important dust components: (1) coal dust from an open-pit mine and fly ash particles from a coal-fired power station, (2) diesel soot, (3) traffic dust from metal, tire and pavement abrasion, and (4) limestone-derived dust. Outside of the coal-mining area, traffic-derived dust defines the atmospheric baseline composition of the studied environment.

  17. Age determinations and growth rates of Pacific ferromanganese deposits using strontium isotopes

    USGS Publications Warehouse

    Ingram, B.L.; Hein, J.R.; Farmer, G.L.

    1990-01-01

    87Sr 86Sr ratios, trace element and REE compositions, and textural characteristics were determined for three hydrogenetic Fe-Mn crusts, one hydrothermal deposit, and two mixed hydrothermalhydrogenetic crusts from the Pacific. The Sr isotope data are compared to the Sr seawater curve for the Cenozoic to determine the ages and growth rates of the crusts. The 87Sr 86Sr in the crusts does not increase monotonically with depth as expected if the Sr were solely derived from seawater and perfectly preserved since deposition. This indicates post-depositional exchange of Sr or heterogeneous sources for the Sr originally contained in the crusts. Textures of hydrogenetic crusts generally correlate with Sr isotopic variations. The highest porosity intervals commonly exhibit the highest 87Sr 86Sr ratios, indicating exchange with younger seawater. Intervals with the lowest porosity commonly have lower 87Sr 86Sr and may preserve the original Sr isotopic ratios. Minimum ages of crust growth inception were calculated from dense, low porosity intervals. Growth of the hydrogenetic crusts began at or after 23 Ma, although their substrates are Cretaceous. Estimated average growth rates of the three hydrogenetic crusts vary between 0.9 and 2.7 mm/Ma, consistent with published rates determined by other techniques. Within the Marshall Islands crust, growth rates for individual layers varied greatly between 1.0 and 5.4 mm/Ma. For one crust, very low 87Sr 86Sr ratios occurred in detrital-rich intervals. Hydrothermal Fe-Mn oxide from the active Lau Basin back-arc spreading axis (Valu Fa Ridge) has an 87Sr 86Sr ratio with a predominantly seawater signature ( 87Sr 86Sr 0.709196), indicating a maximum age of 0.9 Ma. One crust from an off-axis seamount west of Gorda Ridge may have begun precipitating hydrogenetically at 0.5 Ma (0.709211), and had increasing hydrothermal or volcanic input in the top half of the crust, indicated by a significantly lower 87Sr 86Sr ratio (0.709052). ?? 1990.

  18. SU-F-I-56: High-Precision Gamma-Ray Analysis of Medical Isotopes

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Chopra, N; Chillery, T; Chowdhury, P

    2016-06-15

    Purpose: Advanced, time-resolved, Compton-suppressed gamma-ray spectroscopy with germanium detectors is implemented for assaying medical isotopes to study the radioactive decay process leading to a more accurate appraisal of the received dose and treatment planning. Lowell’s Array for Radiological Assay (LARA), a detector array that is comprised of six Compton-suppressed high-purity germanium detectors, is currently under development at UMass-Lowell which combines Compton-suppression and time-and-angle correlations to allow for highly efficient and highly sensitive measurements. Methods: Two isotopes produced Brookhaven Linac Isotope Producer (BLIP) were investigated. {sup 82}Sr which is the parent isotope for producing {sup 82}Rb is often used in cardiacmore » PET. {sup 82}Sr gamma-ray spectrum is dominated by the 511keV photons from positron annihilation which prevent precise measurement of co-produced contaminant isotopes. A second project was to investigate the production of platinum isotopes. Natural platinum was bombarded with protons from 53MeV to 200MeV. The resulting spectrum was complicated due to the large number of stable platinum isotopes in the target, the variety of open reaction channels (p,xn), (p,pxn), (p,axn). Results: By using face-to-face NaI(Tl) counters 90-degrees to the Compton-suppressed germaniums to detect the 511keV photons, a much cleaner and more sensitive measurement of {sup 85}Sr and other contaminants was obtained. For the platinum target, we identified the production of {sup 188–189–191–195}Pt, {sup 191–192–193–194–195–196}Au and {sup 186–188–189–190–192–194–189–190–192–194}Ir. For example, at the lower energies (53 and 65MeV), we measured {sup 191}Pt production cross-sections of 144mb and 157mb. Considerable care was needed in following the process of dissolving and diluting the samples to get consistent results. The new LARA array will help us better ascertain the absolute efficiency of the

  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:

    USGS Publications Warehouse

    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. Geochronology, geochemistry and Sr-Nd-Pb-Hf isotopes of the Early Jurassic granodiorite from the Sankuanggou intrusion, Heilongjiang Province, Northeastern China: Petrogenesis and geodynamic implications

    NASA Astrophysics Data System (ADS)

    Deng, Ke; Li, Qiugen; Chen, Yanjing; Zhang, Cheng; Zhu, Xuefeng; Xu, Qiangwei

    2018-01-01

    Mesozoic granitoid rocks represent a volumetrically component of the Northeastern (NE) China and preserve useful information about the tectonomagmatic history of this region. The Sankuanggou intrusion associated with skarn Fe-Cu deposit in the Duobaoshan ore field within NE China primarily consists of granodiorite with minor alkali-feldspar granite and diorite, which intrudes the Ordovician Duobaoshan Formation in the region. Zircon LA-ICP-MS U-Pb geochronology and whole-rock geochemistry, and Sr-Nd-Pb-Hf isotope analysis were performed on the Sankuanggou intrusion to investigate the petrogenesis and geodynamic implications. Zircon U-Pb dating of magmatic zircons from the granodiorite rock suggests that the intrusion was emplaced in the Early Jurassic (177 ± 1 Ma). Geochemically, it belongs to the metaluminous to slightly peraluminous high-K calc-alkaline I-type granitoids with a narrow range of SiO2 concentration (65.73-67.33 wt.%), high Ba, Sr, LREE and LILE contents and low abundance of Rb, Y, HREE and HFSE. All of these studied samples have homogeneous initial isotope traits with (87Sr/86Sr)i ranging from 0.70415 to 0.70423, εNd(t) of + 3.6 to + 4.0, (206Pb/204Pb)i = 17.933-18.458, (207Pb/204Pb)i = 15.520-15.587 and (208Pb/204Pb)i = 37.523-38.087, and zircon εHf(t) values varying from + 4.8 to + 9.9. These results, combined with the previous data, demonstrate that the Sankuanggou granitoids were formed by partial melting of the pre-existing juvenile crust in an extensional regime related to the post-collisional setting following the closure of the CAOB rather than previously proposed continental arc setting related to Paleo-Pacific or the Mongol-Okhotsk subduction, although their potential influence should not be dismissed.

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

    NASA Astrophysics Data System (ADS)

    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 CAI<2 were chosen for in-situ strontium isotope analysis using laser-ablation multi-collector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS). Conodont samples are from totally 25 layers in seven conodont zones making it possible for a high resolution 87Sr/ 86Sr curve reconstruction during the Permian-Triassic transition. 87Sr/ 86Sr ratio kept a relatively high value (0.70752) in the middle part of the Clarkina yini zone and a lower value (0.70634) in the upperpart of Clarkina taylorae zone. Of which, 87Sr/ 86Sr ratio emerged a rapid decrease within the Clarkina taylorae zone. After a subsequent increase, 87Sr/ 86Sr ratio dropped to 0.70777 in the Isarcicella staeschei zone. These results helps providing reference data for the biological mass extinction 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

  2. Isotope geochronology of the Precambrian

    NASA Astrophysics Data System (ADS)

    Levskii, L. K.; Levchenkov, O. A.

    This symposium discusses the use of isotope methods for establishing the geochronology of Precambrian formations, with special consideration given to geochronological studies of the early phases of the earth's core evolution in the Baltic and Vitim-Aldan shields and the Enderby Land (Antarctica). Attention is also given to the Early Archean Vodlozero gneiss complex and its structural-metamorphic evolution, the influence of geological events during the Proterozoic on the state of the U-Pb and Rb-Sr systems in the Archean postkinematic granites of Karelia, the Rb-Sr systems in the andesite basalts of the Suna-Semch' region (Karelia), and the geochronology of the Karelian granite-greenstone region. Also discussed are the petrogenesis and age of the rocks from the Kola ultradeep borehole, the isotope-geochronological evidence for the early Precambrian history of the Aldan-Olekma region, the Rb-Sr systems in metasedimentary rocks of the Khani graben, and the U-Pb ages of zircons from polymetamorphic rocks of the Archean granulite complex of Enderby Land.

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

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Wall, Andrew J.; Capo, Rosemary C.; Stewart, Brian W.

    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.

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

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Hakala, Jacqueline Alexandra

    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.

  5. Final Progress Report: Isotope Identification Algorithm for Rapid and Accurate Determination of Radioisotopes Feasibility Study

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Rawool-Sullivan, Mohini; Bounds, John Alan; Brumby, Steven P.

    2012-04-30

    This is the final report of the project titled, 'Isotope Identification Algorithm for Rapid and Accurate Determination of Radioisotopes,' PMIS project number LA10-HUMANID-PD03. The goal of the work was to demonstrate principles of emulating a human analysis approach towards the data collected using radiation isotope identification devices (RIIDs). It summarizes work performed over the FY10 time period. The goal of the work was to demonstrate principles of emulating a human analysis approach towards the data collected using radiation isotope identification devices (RIIDs). Human analysts begin analyzing a spectrum based on features in the spectrum - lines and shapes that aremore » present in a given spectrum. The proposed work was to carry out a feasibility study that will pick out all gamma ray peaks and other features such as Compton edges, bremsstrahlung, presence/absence of shielding and presence of neutrons and escape peaks. Ultimately success of this feasibility study will allow us to collectively explain identified features and form a realistic scenario that produced a given spectrum in the future. We wanted to develop and demonstrate machine learning algorithms that will qualitatively enhance the automated identification capabilities of portable radiological sensors that are currently being used in the field.« less

  6. Strontium isotope systematics of scheelite and apatite from the Felbertal tungsten deposit, Austria - results of in-situ LA-MC-ICP-MS analysis

    NASA Astrophysics Data System (ADS)

    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

  7. Kinetic and mineralogic controls on the evolution of groundwater chemistry and 87Sr/86Sr in a sandy silicate aquifer, northern Wisconsin, USA

    USGS Publications Warehouse

    Bullen, T.D.; Krabbenhoft, D.P.; Kendall, C.

    1996-01-01

    Substantial flowpath-related variability of 87Sr/86Sr is observed in groundwaters collected from the Trout Lake watershed of northern Wisconsin. In the extensive shallow aquifer composed of sandy glacial outwash, groundwater is recharged either by seepage from lakes or by precipitation that infiltrates the inter-lake uplands. 87Sr/86Sr of groundwater derived mainly as seepage from a precipitation-dominated lake near the head of the watershed decreases with progressive water chemical evolution along its flowpath due primarily to enhanced dissolution of relatively unradiogenic plagioclase. In contrast, 87Sr/86Sr of groundwater derived mainly from precipitation that infiltrates upland areas is substantially greater than that of precipitation collected from the watershed, due to suppression of plagioclase dissolution together with preferential leaching of Sr from radiogenic phases such as K-feldspar and biotite. The results of a column experiment that simulated the effects of changing residence time of water in the aquifer sand indicate that mobile waters obtain relatively unradiogenic Sr, whereas stagnant waters obtain relatively radiogenic Sr. Nearly the entire range of strontium-isotope composition observed in groundwaters from the watershed was measured in the experimental product waters. The constant mobility of water along groundwater recharge flowpaths emanating from the lakes promotes the dissolution of relatively unradiogenic plagioclase, perhaps due to effective dispersal of clay mineral nuclei resulting from dissolution reactions. In contrast, episodic stagnation in the unsaturated zone along the upland recharge flowpaths suppresses plagioclase dissolution, perhaps due to accumulation of clay mineral nuclei on its reactive surfaces. Differences in redox conditions along these contrasting flowpaths probably enhance the observed differences in strontium isotope behavior. This study demonstrates that factors other than the calculated state of mineral saturation

  8. Mineralogy, geochemistry, and Sr-Pb isotopic geochemistry of hydrothermal massive sulfides from the 15.2°S hydrothermal field, Mid-Atlantic Ridge

    NASA Astrophysics Data System (ADS)

    Wang, Hao; Li, Xiaohu; Chu, Fengyou; Li, Zhenggang; Wang, Jianqiang; Yu, Xing; Bi, Dongwei

    2018-04-01

    The 15.2°S hydrothermal field is located at 15.2°S, 13.4°W within the Mid-Atlantic Ridge (MAR) and was initially discovered during Cruise DY125-22 by the Chinese expedition during R/V Dayangyihao in 2011. Here, we provide detailed mineralogical, bulk geochemical, and Sr-Pb isotopic data for massive sulfides and basalts from the 15.2°S hydrothermal field to improve our understanding of the mineral compositions, geochemical characteristics, type of hydrothermal field, and the source of metals present at this vent site. The samples include 14 massive sulfides and a single basalt. The massive sulfides are dominated by pyrite with minor amounts of sphalerite and chalcopyrite, although a few samples also contain minor amounts of gordaite, a sulfate mineral. The sulfides have bulk compositions that contain low concentrations of Cu + Zn (mean 7.84 wt%), Co (mean 183 ppm), Ni (mean 3 ppm), and Ba (mean 16 ppm), similar to the Normal Mid-Ocean Ridge Basalt (N-MORB) type deposits along the MAR but different to the compositions of the Enriched-MORB (E-MORB) and ultramafic type deposits along this spreading ridge. Sulfides from the study area have Pb isotopic compositions (206Pb/204Pb = 18.4502-18.4538, 207Pb/204Pb = 15.4903-15.4936, 208Pb/204Pb = 37.8936-37.9176) that are similar to those of the basalt sample (206Pb/204Pb = 18.3381, 207Pb/204Pb = 15.5041, 208Pb/204Pb = 37.9411), indicating that the metals within the sulfides were derived from leaching of the surrounding basaltic rocks. The sulfides also have 87Sr/86Sr ratios (0.708200-0.709049) that are much higher than typical MAR hydrothermal fluids (0.7028-0.7046), suggesting that the hydrothermal fluids mixed with a significant amount of seawater during massive sulfide precipitation.

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

    NASA Astrophysics Data System (ADS)

    Betton, P. J.; Civetta, L.

    1984-11-01

    Neodymium isotope and REE analyses of recent volcanic rocks and spinel lherzolite nodules from the Afar area are reported. The 143Nd/ 144Nd ratios of the volcanic rocks range from 0.51286 to 0.51304, similar to the range recorded from Iceland. However, the 87Sr/ 86Sr 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 143Nd/ 144Nd ratios (ca. 0.5129) but varied 87Sr/ 86Sr ratios in the range 0.70427-0.70528. The Sr sbnd 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 87Sr/ 86Sr ratio cannot have been produced by simple processes of partial melting and mixing within normal mantle. Instead the high 87Sr/ 86Sr 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 87Sr/ 86Sr ratio.

  10. Sr and Nd isotopic compositions, age and petrogenesis of A-type granitoids of the Vernon Supersuite, New Jersey Highlands, USA

    USGS Publications Warehouse

    Volkert, R.A.; Feigenson, M.D.; Patino, L.C.; Delaney, J.S.; Drake, Avery A.

    2000-01-01

    Voluminous late Mesoproterozoic monzonite through granite of the Vernon Supersuite underlies an area of approximately 1300 km2 in the Highlands of northern New Jersey. The Vernon Supersuite consists of hastingsite ?? biotite-bearing granitoids of the Byram Intrusive Suite (BIS) and hedenbergite-bearing granitoids of the Lake Hopatcong Intrusive Suite (LHIS). These rocks have similar major and trace element abundances over a range of SiO2 from 58 to 75 wt.%, are metaluminous to weakly peraluminous, and have a distinctive A-type chemistry characterized by high contents of Y, Nb, Zr, LREE, and Ga/Al ratios, and low MgO, CaO, Sr and HREE. Whole-rock Rb-Sr isochrons of BIS granite yield an age of 1116 ?? 41 Ma and initial 87Sr/86Sr ratio of 0.70389, and of LHIS granite an age of 1095 ?? 9 Ma and initial 87Sr/86Sr ratio of 0.70520. Both suites have similar initial 143Nd/144Nd ratios of 0.511267 to 0.511345 (BIS) and 0.511359 to 0.511395 (LHIS). Values of ??(Nd) are moderately high and range from +1.21 to +2.74 in the BIS and +2.24 +2.95 in the LHIS. Petrographic evidence, field relationships, geochemistry, and isotopic data support an interpretation of comagmatism and the derivation of both suites from a mantle-derived or a juvenile lower crustal parent with little crustal assimilation. Both suites crystallized under overlapping conditions controlled by P-T-f(H(2)O). Lake Hopatcong magma crystallized at a liquidus temperature that approached 900??C and a pressure of about 6 kbar, and remained relatively anhydrous throughout its evolution. Initial P-T conditions of the Byram magma were ??? 850??C and about 5.5 kbar. BIS magma was emplaced contemporaneous with, or slightly preceding LHIS magma, and both magmas were emplaced during a compressional tectonic event prior to granulite facies metamorphism that occurred in the Highlands between 1080 and 1030 Ma. (C) 2000 Elsevier Science B.V. All rights reserved.

  11. The isotopic and chemical evolution of Mount St. Helens

    USGS Publications Warehouse

    Halliday, A.N.; Fallick, A.E.; Dickin, A.P.; Mackenzie, A.B.; Stephens, W.E.; Hildreth, W.

    1983-01-01

    Isotopic and major and trace element analysis of nine samples of eruptive products spanning the history of the Mt. St. Helens volcano suggest three different episodes; (1) 40,000-2500 years ago: eruptions of dacite with ??{lunate}Nd = +5, ??{lunate}Sr = -10, variable ??18O, 206Pb/204Pb ??? 18.76, Ca/Sr ??? 60, Rb/Ba ??? 0.1, La/Yb ??? 18, (2) 2500-1000 years ago: eruptions of basalt, andesite and dacite with ??{lunate}Nd = +4 to +8, ??{lunate}Sr = -7 to -22, variable ??18O (thought to represent melting of differing mantle-crust reservoirs), 206Pb/204Pb = 18.81-18.87, variable Ca/Sr, Rb/Ba, La/Yb and high Zr, (3) 1000 years ago to present day: eruptions of andesite and dacite with ??{lunate}Nd = +6, ??{lunate}Sr = -13, ??18O ???6???, variable 206Pb/204Pb, Ca/Sr ??? 77, Rb/Ba = 0.1, La/Yb ??? 11. None of the products exhibit Eu anomalies and all are LREE enriched. There is a strong correlation between 87Sr/86Sr and differentiation indices. These data are interpreted in terms of a mantle heat source melting young crust bearing zircon and garnet, but not feldspar, followed by intrusion of this crustal reservoir by mantle-derived magma which caused further crustal melting and contaminated the crustal magma system with mafic components. Since 1000 years ago all the eruptions have been from the same reservoir which has displayed a much more gradual re-equilibration of Pb isotopic compositions than other components suggesting that Pb is being transported via a fluid phase. The Nd and Sr isotopic compositions lie along the mantle array and suggest that the mantle underneath Mt. St. Helens is not as depleted as MORB sources. There is no indication of seawater involvement in the source region. ?? 1983.

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

    USGS Publications Warehouse

    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.

  13. Tracking Intercontinental Dust Transport With Radiogenic Isotopes: Hefei, China to California, Spring 2002

    NASA Astrophysics Data System (ADS)

    Christensen, J. N.; Cliff, S. S.; Vancuren, R. A.; Perry, K. D.; Depaolo, D. J.

    2006-12-01

    Research over the past decade has highlighted the importance of intercontinental transport and exchange of atmospheric aerosols, including soil-derived dust and industrial pollutants. Far-traveled aerosols can affect air quality, atmospheric radiative forcing and cloud formation and can be an important component in soils. Principal component analysis of elemental data for aerosols collected over California has identified a persistent Asian soil dust component that peaks with Asian dust storm events [1]. Isotopic fingerprinting can provide an additional and potentially more discriminating tool for tracing sources of dust. For example, the naturally variable isotopic compositions of Sr and Nd reflect both the geochemistry of the dust source and its pre- weathering geologic history. Sr and Nd isotopic data and chemical data have been collected for a time series of PM2.5 filter samples from Hefei, China taken from eraly April into early May, 2002. This period encompassed a series of dust storms. The sampling time frame overlapped with the 2002 Intercontinental Transport and Chemical Transformation (ITCT-2K2) experiment along the Pacific coast of North America and inland California. Highs in 87Sr/86Sr in the Hefei time series coincide with peaks in Ca and Si representing peaks in mineral particulate loading resulting from passing dust storms. Mixing diagrams combining isotopic data with chemical data identify several components; a high 87Sr/86Sr component that we identify with mineral dust (loess), and two different low 87Sr/86Sr components (local sources and marine aerosol). Using our measured isotopic composition of the "loess" standard CJ-1 [2] as representative of the pure high 87Sr/86Sr component, we calculate 24 hour average loess particulate concentrations in air which range up to 35 micrograms per cubic meter. Marine aerosol was a major component on at least one of the sampled days. The results for the Hefei samples provide a basis for our isotopic study of

  14. Quantification of spatial and seasonal variations in the proportional contribution of nitrate sources using a multi-isotope approach and Bayesian isotope mixing model.

    PubMed

    Meghdadi, Aminreza; Javar, Narmin

    2018-04-01

    Spatial and seasonal variations in nitrate contamination are a globally concern. While numerous studies have used δ 15 N-NO 3 and δ 18 O-NO 3 to elucidate the dominant sources of nitrate in groundwater, this approach has significant limitations due to the overlap of nitrate isotopic ranges and the occurrence of nitrate isotopic fractionation. This study quantitatively assessed the spatial and seasonal variations in the proportional contributions of nitrate sources from different land uses in the Tarom watershed in North-West Iran. To achieve this aim, orthogonal projection of the hydrochemical and isotopic dataset of the principal component analysis (PCA) as well as correlation coefficient matrix (Corr-PCA) were evaluated to reduce the dimensionality of the inter-correlated dataset. Next, a nitrate isotopic biplot accompanied with a Bayesian isotope mixing model (SIAR) were applied to specify the spatial and seasonal trends in the proportional contribution of three dominant sources of nitrate (fertilizers, animal manure and residential waste) in the watershed. Finally, in order to provide a sensitive framework for nitrate source appointment and overcome the associated limitations of dual nitrate isotope application, the integration of boron isotope (δ 11 B) and strontium isotopic ratio ( 87 Sr/ 86 Sr) was introduced. The results revealed that the mean contribution of residential sewage increased (17%-27.5%), while the mean contribution of fertilizers decreased (28.3%-19%), from late spring to early autumn. Also, fertilizer was the highest contributor (42.1% ± 3.2) during late spring, especially in regions with more than 75% agricultural land. Meanwhile, the mean contribution of sewage was highest in early autumn (32.1% ± 2.8) in the areas with more than 20% residential land. These results were confirmed by coupled application of δ 11 B and 87 Sr/ 86 Sr. This study provides a useful insight for environmental managers to verify groundwater pollution

  15. Isotopic geochemistry of Panama rivers

    USGS Publications Warehouse

    Harmon, Russell S.; Worner, Gerhard; Pribil, Michael; Kern, Zoltan; Forizs, Istvan; Lyons, W. Berry; Gardner, Christopher B.; Goldsmith, Steven T.

    2015-01-01

    River water samples collected from 78 watersheds rivers along a 500-km transect across a Late Cretaceous-Tertiary andesitic volcanic arc terrane in west-central Panama provide a synoptic overview of riverine geochemistry, chemical denudation, and CO2 consumption in the tropics. D/H and 18O/16O relationships indicate that bedrock dissolution of andesitic arc crust in Panama is driven by water-rock interaction with meteoric precipitation as it passes through the critical zone, with no evidence of a geothermal or hydrothermal input. Sr-isotope relationships suggest a geochemical evolution for Panama riverine waters that involves mixing of bedrock pore water with water having 87Sr/86Sr ratios between 0.7037-0.7043 and relatively high Sr-contents with waters of low Sr content that enriched in radiogenic Sr that are diluted by infiltrating rainfall to variable extents.

  16. Controls over δ44/40Ca and Sr/Ca variations in coccoliths: New perspectives from laboratory cultures and cellular models

    NASA Astrophysics Data System (ADS)

    Mejía, Luz María; Paytan, Adina; Eisenhauer, Anton; Böhm, Florian; Kolevica, Ana; Bolton, Clara; Méndez-Vicente, Ana; Abrevaya, Lorena; Isensee, Kirsten; Stoll, Heather

    2018-01-01

    Coccoliths comprise a major fraction of the global carbonate sink. Therefore, changes in coccolithophores' Ca isotopic fractionation could affect seawater Ca isotopic composition, affecting interpretations of the global Ca cycle and related changes in seawater chemistry and climate. Despite this, a quantitative interpretation of coccolith Ca isotopic fractionation and a clear understanding of the mechanisms driving it are not yet available. Here, we address this gap in knowledge by developing a simple model (CaSri-Co) to track coccolith Ca isotopic fractionation during cellular Ca uptake and allocation to calcification. We then apply it to published and new δ 44 / 40 Ca and Sr/Ca data of cultured coccolithophores of the species Emiliania huxleyi and Gephyrocapsa oceanica. We identify changes in calcification rates, Ca retention efficiency and solvation-desolvation rates as major drivers of the Ca isotopic fractionation and Sr/Ca variations observed in cultures. Higher calcification rates, higher Ca retention efficiencies and lower solvation-desolvation rates increase both coccolith Ca isotopic fractionation and Sr/Ca. Coccolith Ca isotopic fractionation is most sensitive to changes in solvation-desolvation rates. Changes in Ca retention efficiency may be a major driver of coccolith Sr/Ca variations in cultures. We suggest that substantial changes in the water structure strength caused by past changes in temperature could have induced significant changes in coccolithophores' Ca isotopic fractionation, potentially having some influence on seawater Ca isotopic composition. We also suggest a potential effect on Ca isotopic fractionation via modification of the solvation environment through cellular exudates, a hypothesis that remains to be tested.

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

    NASA Astrophysics Data System (ADS)

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

    2015-04-01

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

  18. Development and Deployment of a Portable Water Isotope Analyzer for Accurate, Continuous and High-Frequency Oxygen and Hydrogen Isotope Measurements in Water Vapor and Liquid Water

    NASA Astrophysics Data System (ADS)

    Dong, Feng; Baer, Douglas

    2010-05-01

    Stable isotopes of water in liquid and vapor samples are powerful tracers to investigate the hydrological cycle and ecological processes. Therefore, continuous, in-situ and accurate measurements of del_18O and del_2H are critical to advance the understanding of water cycle dynamics around the globe. Furthermore, the combination of meteorological techniques and high-frequency isotopic water measurements can provide detailed time-resolved information on the eco-physiological performance of plants and enable improved understanding of water fluxes at ecosystem scales. In this work, we present recent laboratory development and field deployment of a novel Water Vapor Isotope Analyzer (WVIA), based on cavity enhanced laser absorption spectroscopy, capable of simultaneous in-situ measurements of del_18O and del_2H and water mixing ratio with high precision and high frequency (up to 10 Hz measurement rate). In addition, to ensure the accuracy of the water vapor isotope measurements, a novel Water Vapor Isotope Standard Source (WVISS), based on the instantaneous evaporation of micro-droplets of liquid water (with known isotope composition), has been developed to provide the reference water vapor with widely adjustable mixing ratio (500-30,000 ppmv) for real-time calibration of the WVIA. The comprehensive system that includes the WVIA and WVISS has been validated in extensive laboratory and field studies to be insensitive to ambient temperature changes (5-40 C) and to changes in water mixing ratio over a wide range of mixing ratios. In addition, by operating in the dual inlet mode, measurement drift has essentially been eliminated. The system (WVIA+WVISS) has also been deployed for long-term unattended continuous measurements in the field. In addition to water vapor isotope measurements, the new Water Vapor Isotopic Standard Source (WVISS) may be combined with the WVIA to provide continuous isotopic measurements of liquid water samples at rapid data rate. The availability of

  19. Systematics of nuclear ground state properties in 78-100Sr by laser spectroscopy

    NASA Astrophysics Data System (ADS)

    Buchinger, F.; Ramsay, E. B.; Arnold, E.; Neu, W.; Neugart, R.; Wendt, K.; Silverans, R. E.; Lievens, P.; Vermeeren, L.; Berdichevsky, D.; Fleming, R.; Sprung, D. W. L.; Ulm, G.

    1990-06-01

    Hyperfine structures and isotope shifts of strontium isotopes with A=78 to A=98 and A=100 were measured by collinear fast beam laser spectroscopy. Nuclear spins, moments and changes in mean square charge radii are extracted from the data. The spins and moments of most of the odd isotopes are explained in the framework of the single particle model. The changes in mean square charge radii are compared with predictions of the droplet model and of Hartree-Fock-plus-BCS calculations. For the isotopes in the transitional regions below and above the N=50 shell closure, the inclusion of quadrupole zero point motion in the Droplet model describes part of the observed shell effect. An additional change in the surface region of the charge distribution at spherical shape is suggested by the microscopic model. Furthermore, we propose that the isotopes 78Sr and 80Sr may show an unusual shape-sharing structure, with different mean deformations in the ground and 2+1 excited states.

  20. Isotopic evolution of Mauna Loa Volcano: A view from the submarine southwest rift zone

    NASA Astrophysics Data System (ADS)

    Kurz, Mark D.; Kenna, T. C.; Kammer, D. P.; Rhodes, J. Michael; Garcia, Michael O.

    New isotopic and trace element measurements on lavas from the submarine southwest rift zone (SWR) of Mauna Loa continue the temporal trends of subaerial Mauna Loa flows, extending the known compositional range for this volcano, and suggesting that many of the SWR lavas are older than any exposed on land. He and Nd isotopic compositions are similar to those in the oldest subaerial Mauna Loa lavas (Kahuku and Ninole Basalts), while 87Sr/86Sr ratios are slightly lower (as low as .7036) and Pb isotopes are higher (206Pb'204Pb up to 18.30). The coherence of all the isotopes suggests that helium behaves as an incompatible element, and that helium isotopic variations in the Hawaiian lavas are produced by melting and mantle processes, rather than magma chamber or metasomatic processes unique to the gaseous elements. The variations of He, Sr, and Nd are most pronounced in lavas of approximately 10 ka age range [Kurz and Kammer, 1991], but the largest Pb isotopic variation occurs earlier. These variations are interpreted as resulting from the diminishing contribution from the upwelling mantle plume material as the shield building ends at Mauna Loa. The order of reduction in the plume isotopic signature is inferred to be Pb (at >100 ka), He (at ˜14 ka), Sr (at ˜9 ka), and Nd (at ˜8 ka); the different timing may relate to silicate/melt partition coefficients, with most incompatible elements removed first, and also to concentration variations within the plume. Zr/Nb, Sr/Nb, and fractionation-corrected Nb concentrations, correlate with the isotopes and are significantly higher in some of the submarine SWR lavas, suggesting temporal variability on time scales similar to the Pb isotopes (i.e. ˜ 100 ka). Historical lavas define trace element and isotopic trends that are distinct from the longer term (10 to 100 ka) variations, suggesting that different processes cause the short term variability. The temporal evolution of Mauna Loa, and particularly the new data from the

  1. Sr-isotopic composition of marbles from the Puerto Galera area (Mindoro, Philippines): additional evidence for a Paleozoic age of a metamorphic complex in the Philippine island arc

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Knittel, U.; Daniels, U.

    1987-02-01

    The Sr-isotopic composition of marbles from the Puerto Galera area (Mindoro, Philippines) is compatible with either a Tertiary or a Paleozoic age. The former is considered as unlikely because nonmetamorphic sediments of that age overlie the metamorphic complex. This implies that the metamorphic complex does not represent the basement of the Philippine arc but is an accreted terrane.

  2. 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

    NASA Astrophysics Data System (ADS)

    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

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

    NASA Astrophysics Data System (ADS)

    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

  4. Application of [sup 87]Sr/[sup 86]Sr, [delta][sup 18]O and [delta][sup 13]C isotopes to diagenesis correlation and connectivity of a fractured chalk reservoir, the Sidi El Kilani field, Tunisia

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Mearns, E.W.; McBride, J.J.; Bramwell, M.

    1996-01-01

    Oil is produced primarily from open fracture porosity in Upper Cretaceous chalk in the Sidi El Kilani oil field. Strontium Stratigraphy analyses of primary, unaltered matrix chalk has confirmed a Campanian to Maastrichtian age and has allowed dating of the reservoir with a resolution of [+-]1 Ma. This has facilitated reservoir correlation and has indicated where section is missing in certain wells due to faulting. [sup 87]Sr/[sup 86]Sr, [delta][sup 18]O and [delta][sup 13]C analyses suggest an early generation of fracture fill calcite cement may have formed by redistribution of CaCO[sub 3] from underlying carbonate sequences at temperatures in the regionmore » 35-55[degrees]C. Calcite cemented fractures tend to be healed and are not productive. Strontium Isotope Residual Salt Analyses (SrRSA) conducted on core, provide information on the formation water chemistry and reservoir connectivity at the time of oil filling. These data suggest that the NW-SE trending fault system that bisects the field is sealed across much of the fault plane. The main oil pool lies SW of the fault. A later generation of dolomite and barite cements, associated with productive open fractures, have Sr-O-C composition consistent with precipitation from fluids circulating at the time of hydrocarbon charge at temperatures close to current reservoir conditions of 70-75[degrees]C. Predicting the distribution of dolomite cemented open fractures has thus helped guide the development strategy of the field.« less

  5. Application of {sup 87}Sr/{sup 86}Sr, {delta}{sup 18}O and {delta}{sup 13}C isotopes to diagenesis correlation and connectivity of a fractured chalk reservoir, the Sidi El Kilani field, Tunisia

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Mearns, E.W.; McBride, J.J.; Bramwell, M.

    1996-12-31

    Oil is produced primarily from open fracture porosity in Upper Cretaceous chalk in the Sidi El Kilani oil field. Strontium Stratigraphy analyses of primary, unaltered matrix chalk has confirmed a Campanian to Maastrichtian age and has allowed dating of the reservoir with a resolution of {+-}1 Ma. This has facilitated reservoir correlation and has indicated where section is missing in certain wells due to faulting. {sup 87}Sr/{sup 86}Sr, {delta}{sup 18}O and {delta}{sup 13}C analyses suggest an early generation of fracture fill calcite cement may have formed by redistribution of CaCO{sub 3} from underlying carbonate sequences at temperatures in the regionmore » 35-55{degrees}C. Calcite cemented fractures tend to be healed and are not productive. Strontium Isotope Residual Salt Analyses (SrRSA) conducted on core, provide information on the formation water chemistry and reservoir connectivity at the time of oil filling. These data suggest that the NW-SE trending fault system that bisects the field is sealed across much of the fault plane. The main oil pool lies SW of the fault. A later generation of dolomite and barite cements, associated with productive open fractures, have Sr-O-C composition consistent with precipitation from fluids circulating at the time of hydrocarbon charge at temperatures close to current reservoir conditions of 70-75{degrees}C. Predicting the distribution of dolomite cemented open fractures has thus helped guide the development strategy of the field.« less

  6. Comparison of Two Methods for Determination of Strontium Isotopes in Pore Water at Yucca Mountain, Nevada

    NASA Astrophysics Data System (ADS)

    Marshall, B. D.; Futa, K.; Scofield, K. M.

    2002-12-01

    The proposed radioactive waste repository at Yucca Mountain, Nevada would be constructed in the high-silica rhyolite member of the Topopah Spring Tuff, an ash-flow tuff within the ~500-m-thick unsaturated zone. Dry-drilled rock cores from this unit have been packaged to preserve their water content. Two methods have been used to extract the strontium contained in the pore water for isotopic measurements. In the first method, samples of dried core were crushed, and the 0.25 to 2.4 mm size fractions were leached with ultra-pure water for about 1 hour to dissolve the salts left behind by the evaporated pore water. Concentrations of strontium in the pore water were calculated from determinations of porosity and saturation on adjacent core and the measured strontium concentration in the leachate. In the second method, pore water was extracted from sealed core using an ultracentrifuge, minimizing evaporation of water from the core at all steps in the process. The centrifugation of 150 to 200 g of welded tuff at 15,000 rpm for 6 hours typically results in the recovery of as much as 3 ml of pore water for analysis. Strontium isotope compositions were determined by thermal ionization mass spectrometry; 87Sr /86Sr ratios have a reproducibility of 0.00005. The ranges of 87Sr/86Sr ratios determined by the two methods are identical: 0.71215 to 0.71267 in the leachates (n = 35) and 0.71214 to 0.71266 in the extracted pore waters (n = 21). However, the calculated strontium concentrations in the leachates average 300 μg/L, whereas those in the extracted pore water average 1440 μg/L, indicating that a substantial portion of the pore-water salts remain in the crushed rock after leaching. The strontium data determined on extracted pore water shows that the leaching of pore-water salts results in accurate 87Sr/86Sr, but that a substantial correction to the strontium concentration is required due to the inefficiency of the leaching procedure and the small pore sizes in the welded

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

    NASA Astrophysics Data System (ADS)

    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

  8. Petrogenesis of granodiorite in the Balong region, eastern Kunlun Orogen, China: Constraints from zircon U-Pb geochronology, geochemistry and Sr-Nd-Hf isotopes

    NASA Astrophysics Data System (ADS)

    Huang, X.; Li, H.; Wang, Y.; Liu, Y.

    2017-12-01

    Numerous granitoid intrusions that close to the Balong region have great scientific significance to reveal tectonic evolution and geodynamic background of eastern Kunlun Orogen (EKO). Balong granodiorite (BLG) is located at the northern of the EKO. It generally emplaced into the Proterozoic to Lower Palaeozoic rocks and contains abundant mafic microgranular enclaves. LA-ICP-MS zircon U-Pb dating of the BLG gives a 206Pb/238U age of 230.7±1.9 Ma, indicating that it was emplaced in the Late Triassic. The BLG is high-K calc-alkaline series and metaluminous, with SiO2 of 59.86 61.83%, K2O+Na2O of 5.98 6.40%, CaO of 4.95 5.77% and P2O5 of 0.14% 0.18%. The granodioritic rocks are enriched in LILE (Ba, Rb, Sr), but depleted in HFSE (Nb, Ta, P, Ti), with weak negative Eu anomalies (δEu=0.70 0.82). Mineralogy and geochemistry of the rocks show an affinity to I-type granite. The BLG, having (87Sr/86Sr)i ratios of 0.70819 to 0.70832, ɛNd(t) values of -5.27 to -5.75, and zircon ɛHf(t) values ranging from -3.86 to -1.34. The whole-rock Nd isotopic model ages (1432 1471 Ma) and zircon Hf isotopic model ages (1205 1357 Ma) indicate that the BLG is generated by partial melting of lower crust (Precambrian metabasaltic basement rocks) with different degree of involvement of mantle material. Combined with regional geological data, the granodiorite was derived from dehydration melting of mafic lower crustal rocks during the subduction of the Anyemaqen ocean lithosphere at Late Permian-Triassic in a subduction setting. Basaltic magma underplating and crust-mantle mixing are main mechanisms for the origin of large-scale I-type granitoid in Balong.

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

    NASA Astrophysics Data System (ADS)

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

    2016-09-01

    The Qinling Orogen was a consequence of continental collision of the South China Craton with the North China Craton in the Triassic and caused widespread granitoid magmatism. However, the petrogenesis of these granitoids remains controversial. In this paper, we choose the Baijiazhuang (BJZ) and Lvjing (LJ) plutons in the West Qinling Orogen for a combined study of the zircon U-Pb geochronology, whole-rock major and trace element compositions and Sr-Nd-Hf isotopic characteristics. We obtained zircon crystallization ages of 216 Ma and 212 Ma for the BJZ and the LJ plutons, respectively. The granitoid samples from both plutons have high K2O metaluminous to peraluminous compositions. They are enriched in large ion lithophile elements (LILEs), light rare earth elements (LREEs) and depleted in high field-strength elements (HFSEs) with significant negative Eu anomalies. The BJZ samples have initial Sr isotopic ratios of 0.7032 to 0.7078, εNd(t) of - 10.99 to - 8.54 and εHf (t) of - 10.22 to - 6.41. The LJ granitoids have initial Sr isotopic ratios of 0.7070 to 0.7080, εNd(t) of - 5.37 to - 4.58 and εHf(t) of - 3.64 to - 1.78. The enriched isotopic characteristics of the two plutons are consistent with their source being dominated by ancient continental crust. However, two BJZ samples show depleted Sr isotope compositions, which may infer possible involvement of mantle materials. Mantle-derived melt, which formed from partial melting of mantle wedge peridotite facilitated by dehydration of the subducted/subducting Mianlue ocean crust, provide the required heat for the crustal melting while also contributing to the compositions of these granitoids. That is, the two granitic plutons are magmatic responses to the closure of the Mianlue ocean basin and the continental collision between the Yangtze and South Qinling crustal terranes. (143Nd/144Nd)i = (143Nd/144Nd) - (147Sm/144Nd) × (eλt - 1), εNd(t) = [(143Nd/144Nd) / (143Nd/144Nd)CHUR(t) - 1] × 104, (143Nd/144Nd

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

    PubMed

    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.

  11. High-precision γ -ray spectroscopy of the cardiac PET imaging isotope Rb 82 and its impact on dosimetry

    DOE PAGES

    Nino, M. N.; McCutchan, E. A.; Smith, S. V.; ...

    2016-02-01

    82Rb is a positron-emitting isotope used in cardiac positron emission tomography (PET) imaging which has been reported to deliver a significantly lower effective radiation dose than analogous imaging isotopes like 201Tl and 99mTc sestamibi. High-quality β-decay data are essential to accurately appraise the total dose received by the patients. A source of 82Sr was produced at the Brookhaven Linac Isotope Producer (BLIP), transported to Argonne National Laboratory, and studied with the Gammasphere facility. Significant revisions have been made to the level scheme of 82Kr including 12 new levels, 50 new γ-ray transitions, and the determination of many new spin assignmentsmore » through angular correlations. Lastly, these new high-quality data allow a precise reappraisal of the β-decay strength function and thus the consequent dose received by patients.« less

  12. Isotopic Composition of the Neolithic Alpine Iceman's Tooth Enamel and Clues to his Origin

    NASA Astrophysics Data System (ADS)

    Muller, W.; Muller, W.; Halliday, A. N.

    2001-12-01

    Five small enamel fragments from three teeth of the upper right jaw from the mummy of the Neolithic Alpine Iceman have been investigated for their isotopic composition in order to shed light on his geographic origins. Soils from approximately contemporaneous sites were sampled for comparison. Tooth enamel forms ontogenetically very early and is not re-mineralized during later lifetime (unlike with bone material). Therefore, unique insights into the Iceman's childhood can be acquired. Enamel also is the densest tissue of a human body and is thus less susceptible to post-mortem alteration. Both radiogenic (Sr, Pb, Nd) and stable isotopes (O, C) are investigated. Radiogenic isotopes allow reconstruction of the local geological background, because humans incorporate Sr, Pb and Nd from their local environment by eating local food. Stable isotopes provide information about altitude and/or position relative to the main Alpine watershed. High spatial-resolution laser-ablation ICPMS profiles reveal that most elements are distributed in a manner that is essentially similar to modern human teeth except of that La, Ce, Nd (LREE) show up to a 100-fold enrichment towards the outer enamel surface. These uptake-profiles may reflect interaction with melt water, consistent with data for the composition of samples of the Iceman's skin. Biogenic apatites (enamel, bone) have very low in-vivo LREE concentrations, but take up LREEs post-mortem from the burial environment. Ice core samples from the finding site show concentrations up to 400 ppt Ce. Such high uptake of the LREEs precludes the derivation of an in-vivo Nd isotopic signal, but both other radiogenic tracers, Sr and Pb, show pristine (in-vivo) concentrations of 87 ppm and 0.1 ppm, respectively. Strontium isotopic compositions were determined on fragments from the canine, the first and second premolar (1 - 9 mg) and two hip bone samples, utilizing three sequential leaching steps for each sample to detect possible alteration

  13. Rb-Sr and Sm-Nd chronology and genealogy of mare basalts from the Sea of Tranquility

    NASA Technical Reports Server (NTRS)

    Papanastassiou, D. A.; Depaolo, D. J.; Wasserburg, G. J.

    1977-01-01

    Rb-Sr and Sm-Nd ages of two Apollo 11 mare basalts, high-K basalt 10072 and low-K basalt 10062, are reported. Rb-Sr, Sm-Nd, and Ar-40-Ar-39 ages are in good agreement and indicate an extensive time interval for filling of the Sea of Tranquility, presumably by thin lava flows, in agreement with similar observations for the Ocean of Storms. Initial Sr and Nd isotopic compositions on Apollo 11 basalts reveal at least two parent sources producing basalts. The Sm-Nd isotopic data demonstrate that low-K and high-Ti basalts from Apollo 11 and 17 derived from distinct reservoirs, while low-Ti Apollo 15 mare basalt sources have Sm/Nd similar to the sources of Apollo 11 basalts. Groupings of mare basalt based on Ti content and on isotopic data do not coincide.

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

    NASA Astrophysics Data System (ADS)

    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

  15. Unraveling the hidden origin and migration of plagioclase phenocrysts by in situ Sr isotopes: the case of final dome activity at Nisyros volcano, Greece

    NASA Astrophysics Data System (ADS)

    Braschi, Eleonora; Francalanci, Lorella; Tommasini, Simone; Vougioukalakis, George E.

    2014-03-01

    This contribution reports a detailed study on in situ Sr isotope analyses, along with textural and compositional characteristics, of plagioclase phenocrysts occurring in the rhyodacitic dome-lavas and associated mafic enclaves, erupted during the last magmatic activity at Nisyros volcano (Greece). Dome-lavas and enclaves have a paragenesis dominated by plagioclase. We recognize five different types of plagioclase based on their specific textures and composition. Dome-lava plagioclases (Type-1) are mainly large (1-5 mm), subhedral, clear, and poorly zoned crystals with low An content (An25-35). The plagioclase phenocrysts (Type-4 and Type-5) and groundmass microlites crystallizing in the enclaves, and found in dome-lavas as xenocrysts, have high An content (An75-95). In both dome-lavas and enclaves, two other types of plagioclase do also occur: (1) plagioclase phenocrysts with size and core composition similar to those of Type-1 having a dusty sieve zone (DSZ) at the rims (Type-2); (2) plagioclases with a DSZ affecting the entire crystal but a thin rim (Type-3). The drilled plagioclases have 87Sr/86Sr negatively correlated with their An content. Low An cores of Type-1 and Type-2 have quite homogeneous 87Sr/86Sr (0.7044-0.7046), whose values are more radiogenic than their host magmas (0.70403-0.70408) and similar to those of the previous Upper Pumice (UP) rhyolite magma (0.70438-0.70456). The DSZs of Type-2 and Type-3 show lower and scattered 87Sr/86Sr (0.70397-0.70426) with intermediate and variable An content. High An cores of Type-4 and Type-5 have the least radiogenic Sr isotope composition (0.70379) in equilibrium with that measured in the enclaves (0.70384-0.70389). We demonstrate that Type-1 plagioclase crystallizes in the previous UP rhyolitic magmas representing the silica-rich magma from which the dome-lava melts derived by open system evolutionary processes (e.g., mixing, mingling, and crystal migration), caused by successive refilling of mafic enclave

  16. Rb-Sr and Sm-Nd Isotopic Studies of Martian Depleted Shergottes SaU 094/005

    NASA Technical Reports Server (NTRS)

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

    2007-01-01

    Sayh al Uhaymir (SaU) 094 and SaU 005 are olivine-phyric shergottites from the Oman desert and are considered as pairs. [e.g., 1]. They are very similar to the Libyan desert shergottite Dar al Gani (DaG) 476 in petrology, chemistry and ejection age [2-6]. This group of shergottites, also recognized as depleted shergottites [e.g. 7] has been strongly shocked and contains very low abundances of light rare earth elements (REE). In addition, terrestrial contaminants are commonly present in meteorites found in desert environments. Age-dating these samples is very challenging, but lower calcite contents in the SaU meteorites suggest that they have been subjected to less severe desert weathering than their DaG counterparts [3-4]. In this report, we present Rb-Sr and Sm-Nd isotopic results for SaU 094 and SaU 005, discuss the correlation of their ages with those of other similar shergottites, and discuss their petrogenesis.

  17. Sr-isotopic, paleomagnetic, and biostratigraphic calibration of horse evolution: Evidence from the Miocene of Florida

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    MacFadden, B.J.; Bryant, J.D.; Mueller, P.A.

    1991-03-01

    During the middle Miocene an explosive adaptive radiation resulted in the advent of grazing horses with high-crowned teeth in North America. New Sr isotopic, paleomagnetic, and biostratigrahic evidence from the Miocene marine and nonmarine sequence of the Florida panhandle calibrates the base of this adaptive radiation. The transition from the primitive outgroup species 'Parahippus' leonensis to the most primitive high-crowned horse, 'Merychippus' gunteri occured after about 17.7 Ma. After this event, the lowest known stratigraphic level at which diversification (i.e., presence of two or more sympatric species) of grazing merychippine horses occurs is about 16.2 Ma, or within the earlymore » part of Chron C5BR. Although this currently is the only sequence where the parahippine-merychippine transition is directly calibrated, biochronologic evidence from other important, contemporaneous localities in Texas, Nebraska, and California indicate that diversification occured rapidly throughout North America between 15 and 16 Ma.« less

  18. Post-eruptive alteration of silicic ignimbrites and lavas, Gran Canaria, Canary Islands - Strontium, neodymium, lead, and oxygen isotopic evidence

    NASA Technical Reports Server (NTRS)

    Cousens, Brian L.; Spera, Frank J.; Dobson, Patrick F.

    1993-01-01

    The isotopic composition of lavas from oceanic islands provides important information about the composition and evolution of the earth's mantle. Isotopic analyses of Miocene comenditic, pantelleritic, and trachyphonolitic ignimbrites and lavas from the Canary islands were performed. Results provide evidence for posteruptive mobility of Rb and Sr during low temperature postemplacement interaction with circulating ground water. Calculated Sr isotope ratios define a magmatic trend in the stratigraph section. 87Sr/86Sr ratios in hydrated vitrophyte and devitrified matrix separates indicate significant posteruptive interaction with meteoric water starting soon after deposition. This process extends patchily through the entire pyroclastic flow and may be ongoing. 87Sr/86Sr ratios determined by whole rock analysis of silicic rocks from oceanic islands are suspect and should not be incorporated into mantle tracer studies. Anorthoclase phenocrysts are resistant to these processes and may produce useful data.

  19. 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

    NASA Astrophysics Data System (ADS)

    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

  20. Generation of syntectonic calc-alkaline, magnesian granites through remelting of pre-tectonic igneous sources - U-Pb zircon ages and Sr, Nd and Pb isotope data from the Donkerhoek granite (southern Damara orogen, Namibia)

    NASA Astrophysics Data System (ADS)

    Schwark, L.; Jung, S.; Hauff, F.; Garbe-Schönberg, D.; Berndt, J.

    2018-06-01

    The 541 ± 4 Ma-old magnesian, weakly peraluminous, calc-alkalic Donkerhoek Onanis granite is part of the ca. 6000 km2 large Donkerhoek batholith in the Southern Zone of the Damara orogen of Namibia. Linear major and trace element variations and decreasing MgO, FeO, Al2O3, CaO, K2O, Na2O, Ba and Sr concentrations with increasing SiO2 indicate that this part of the batholith represent a coherent mass and underwent fractional crystallization processes. The Donkerhoek Onanis granites are isotopically evolved (initial εNd: -4.7 to -12.3, initial 87Sr/86Sr: 0.7099-0.7157) with moderately radiogenic Pb isotope ratios (206Pb/204Pb: 17.26-18.22; 207Pb/204Pb: 15.59-15.67; 208Pb/204Pb: 37.60-38.06). Beside heterogeneities imparted by the sources, an evaluation of LREE fractionation and Nd isotope data suggests that AFC processes also modified some samples. Based on the chemical and isotope data, the Donkerhoek Onanis granites cannot be derived by partial melting of Al- and Fe-rich metasedimentary rocks of the Kuiseb formation in which they intruded. Instead, melting of meta-igneous crustal sources with Proterozoic crustal residence ages is more likely. Three igneous to meta-igneous rock suites from the area (Matchless amphibolites, Proterozoic mafic to felsic gneisses from the southern Kalahari craton basement, syn-tectonic Salem granodiorites to granites) are potential sources. An evaluation of chemical and isotope data suggests that remelting of early syn-orogenic Salem-type granites is the most likely process which would also explain the existence of ca. 563 ± 4 Ma-old zircon in the Donkerhoek Onanis granites. Comparison of the Donkerhoek Onanis granites with experimentally derived melt compositions from an intermediate igneous parent indicates temperatures between 800 and 850 °C. It is suggested that the Pan-African igneous activity in this part of the Damara Belt was a moderate-temperature intra-crustal event. Although there are some compositional similarities with

  1. The Dissolved Ca Isotope Composition of Himalayan-Tibetan Waters

    NASA Astrophysics Data System (ADS)

    Tipper, E. T.; Galy, A.; Bickle, M. J.

    2004-12-01

    Determining the relative proportions of carbonate versus silicate weathering in the Himalaya is important for understanding the long-term atmospheric CO2 budget and the marine Sr isotope record. 87Sr/86Sr is not a straightforward proxy of carbonate to silicate weathering in the Himalaya and up to 50% of the dissolved Ca may be removed by the precipitation of secondary calcite. Ca isotopes have the potential to constrain the relative inputs of carbonates to silicates and incongruent dissolution processes in the weathering environment. Ca is the major cation carried by rivers. Thirty four Himalayan rock and water samples from the Nepal Himalaya and Tibet have been analysed for 44/42Ca and 43/42Ca on a Nu-Instruments Multiple Collector -ICP-MS. Unlike the 44/40Ca ratio the 44/42Ca is not susceptible to excess 40Ca production from the decay of K. All samples lie on a single mass fractionation line. There is a total range of 0.4 \\permil variation in \\delta44Ca with values from 0.63 \\permil - 0.21 \\permil relative to the SRM915a standard. This is comparable to that already reported with \\delta44/40Ca for small catchments and global rivers. Small first order catchments from each of the main lithotectonic units of the Himalaya have been analysed to examine the effect of lithology on dissolved Ca isotopic composition. In agreement with previous studies elsewhere there is little correlation between source rock and dissolved composition for small rivers spanning a range of source rock from limestone to various silicates and covering a vegetation range from temperate semi-desert to jungle. \\delta44Ca is not correlated with 87Sr/86Sr or Na/Ca ratios confirming that source rock composition is not the dominant control on the observed range in \\delta44Ca. A time-series has been examined for the Marsyandi River, central Nepal. In spite of significant systematic variations in major element chemistry including Ca concentration and 87Sr/86Sr the variations in \\delta44Ca are

  2. Chemical and Sr isotopic characteristics of rainwater on the Alxa Desert Plateau, North China: Implication for air quality and ion sources

    NASA Astrophysics Data System (ADS)

    Rao, Wenbo; Han, Guilin; Tan, Hongbing; Jin, Ke; Wang, Shuai; Chen, Tangqing

    2017-09-01

    The major ions and Sr isotopes in rainwater have been studied during 2013-2015 on the Alxa Desert Plateau in order to identify the source of rainwater chemistry and to assess air quality in the desert area of northern China. The pH and EC values of rainwater vary from 6.7 to 8.1 and from 35 to 1237 μS cm- 1, respectively, at the two meteorological stations (AYQ and YBL) in the Alxa Desert Plateau. Ca2 +, SO42 -, Na+ and Cl- are the dominant ions in rainwater, possessing > 85% of total ions. The mean daily wet deposition fluxes of soluble ions are 8709 μeq/m2/d at YBL and 5459 μeq/m2/d at AYQ, approaching the values at Xi'an, Beijing, Guangzhou, and Chengdu. Statistical analysis shows that SO42 - and NO3- in rainwater were mainly from anthropogenic sources while Ca2 + and K+ originated from terrestrial sources. Cl- was mainly from seawater sources, and Na+ was partly from mineral weathering. Major ions are well correlated with each other in rainwater, revealing that substances of various origins were synchronously carried into the atmosphere by wind. By using Sr isotope techniques, three main end-members controlling base cations of rainwater are identified: silicates, carbonates and seawater. Based on the analyses of acid-soluble fractions of desert soils, local soil dust could be the most important source of base cations in rainwater whereas the effect of the anthropogenic sources could be neglected.

  3. Carbon, oxygen, and strontium isotopic composition of methane-derived authigenic carbonates in methane seep areas, eastern margin of Japan Sea

    NASA Astrophysics Data System (ADS)

    Kakizaki, Y.; Ishikawa, T.; Hiruta, A.; Matsumoto, R.

    2016-12-01

    We report the occurrence, mineralogy, and isotopic composition (δ13C; δ18O) of methane-derived authigenic carbonates (MDACs) from three methane seep areas with shallow gas hydrate (Umitaka Spur, Joetsu Knoll, and off-Tobishima Island), in the southeastern margin of Japan Sea. Furthermore, we present strontium isotopic ratios (87Sr/86Sr) of MDACs, pore waters, and seawater from Umitaka Spur. MDACs range from a few mm to several tens of cm in diameter. Their shape is quite varied, e.g. nodular, platy, and indetermine form. Most MDACs are composed of high-Mg calcite. The δ13C values of MDACs from Umitaka Spur range from -30 to -4 permil. These isotopic values are higher than those of Joetsu Knoll and off-Tobishima Island. This difference is dependent upon the formation depth of MDACs in the sediment column. It probably indicates a difference in the formation environment of MDACs (e.g. methane flux). Meanwhile, range of the δ18O values of MDACs from those three areas is mostly equal. The 87Sr/86Sr ratios in MDACs from shallow sediment depth of Umitaka Spur are equal to those of modern surface seawater just above Umitaka Spur. The 87Sr/86Sr ratios of MDACs from deeper sediment depth are lower, and the Sr-isotopic trend indicates an upward increase. This trend can be correlated to the global Sr-isotopic trend of the seawater from late Pleistocene to present. It means that 87Sr/86Sr ratios of MDACs reflect the 87Sr/86Sr ratio of seawater at the formation age. However, the 87Sr/86Sr ratios in pore water are lower than those of MDACs, yet follow a parallel trend. This would suggest that the pore water includes a source of light Sr, presumably released from tuff and volcaniclastics during diagenetic processes. This study was conducted under the commission from AIST as a part of the methane hydrate research project funded by METI (the Ministry of Economy, Trade and Industry, Japan).

  4. Geochemical and multi-isotopic ( 87Sr/ 86Sr, 143Nd/ 144Nd, 238U/ 235U) perspectives of sediment sources, depositional conditions, and diagenesis of the Marcellus Shale, Appalachian Basin, USA

    DOE PAGES

    Phan, Thai T.; Gardiner, James B.; Capo, Rosemary C.; ...

    2017-10-25

    Here, we investigate sediment sources, depositional conditions and diagenetic processes affecting the Middle Devonian Marcellus Shale in the Appalachian Basin, eastern USA, a major target of natural gas exploration. Multiple proxies, including trace metal contents, rare earth elements (REE), the Sm-Nd and Rb-Sr isotope systems, and U isotopes were applied to whole rock digestions and sequentially extracted fractions of the Marcellus shale and adjacent units from two locations in the Appalachian Basin. The narrow range of εNd values (from –7.8 to –6.4 at 390 Ma) is consistent with derivation of the clastic sedimentary component of the Marcellus Shale from amore » well-mixed source of fluvial and eolian material of the Grenville orogenic belt, and indicate minimal post-depositional alteration of the Sm-Nd system. While silicate minerals host >80% of the REE in the shale, data from sequentially extracted fractions reflect post-depositional modifications at the mineralogical scale, which is not observed in whole rock REE patterns.« less

  5. Geochemical and multi-isotopic ( 87Sr/ 86Sr, 143Nd/ 144Nd, 238U/ 235U) perspectives of sediment sources, depositional conditions, and diagenesis of the Marcellus Shale, Appalachian Basin, USA

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Phan, Thai T.; Gardiner, James B.; Capo, Rosemary C.

    Here, we investigate sediment sources, depositional conditions and diagenetic processes affecting the Middle Devonian Marcellus Shale in the Appalachian Basin, eastern USA, a major target of natural gas exploration. Multiple proxies, including trace metal contents, rare earth elements (REE), the Sm-Nd and Rb-Sr isotope systems, and U isotopes were applied to whole rock digestions and sequentially extracted fractions of the Marcellus shale and adjacent units from two locations in the Appalachian Basin. The narrow range of εNd values (from –7.8 to –6.4 at 390 Ma) is consistent with derivation of the clastic sedimentary component of the Marcellus Shale from amore » well-mixed source of fluvial and eolian material of the Grenville orogenic belt, and indicate minimal post-depositional alteration of the Sm-Nd system. While silicate minerals host >80% of the REE in the shale, data from sequentially extracted fractions reflect post-depositional modifications at the mineralogical scale, which is not observed in whole rock REE patterns.« less

  6. Linking Barbados Mineral Dust Aerosols to North African Sources Using Elemental Composition and Radiogenic Sr, Nd, and Pb Isotope Signatures

    NASA Astrophysics Data System (ADS)

    Bozlaker, Ayse; Prospero, Joseph M.; Price, Jim; Chellam, Shankararaman

    2018-01-01

    Large quantities of African dust are carried across the Atlantic to the Caribbean Basin and southern United States where it plays an important role in the biogeochemistry of soils and waters and in air quality. Dusts' elemental and isotopic composition was comprehensively characterized in Barbados during the summers of 2013 and 2014, the season of maximum dust transport. Although total suspended insoluble particulate matter (TSIP) mass concentrations varied significantly daily and between the two summers, the abundances (μg element/g TSIP) of 50 elements during "high-dust days" (HDD) were similar. Aerosols were regularly enriched in Na, Cu, Zn, As, Se, Mo, Cd, Sn, Sb, and W relative to the upper continental crust. Enrichment of these elements, many of which are anthropogenically emitted, was significantly reduced during HDD, attributed to mixing and dilution with desert dust over source regions. Generally, Ti/Al, Si/Al, Ca/Al, Ti/Fe, Si/Fe, and Ca/Fe ratios during HDD differed from their respective values in hypothesized North African source regions. Nd isotope composition was relatively invariant for "low-dust days" (LDD) and HDD. In contrast, HDD-aerosols were more radiogenic exhibiting higher 87Sr/86Sr, 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios compared to LDD. Generally, Barbados aerosols' composition ranged within narrow limits and was much more homogeneous than that of hypothesized African source soils. Our results suggest that summertime Barbados aerosols are dominated by a mixture of particles originating from sources in the Sahara-Sahel regions. The Bodélé Depression, long suspected as a major source, appears to be an insignificant contributor of summertime western Atlantic dust.

  7. The clay mineral and Sr-Nd isotopic composition for fine-grained fraction of sediments from northwestern South China Sea: implications for sediment provenance

    NASA Astrophysics Data System (ADS)

    Cai, G.

    2013-12-01

    *Guanqiang Cai caiguanqiang@sina.com Guangzhou Marine Geological Survey, Guangzhou, 510760, P.R. China As the largest marginal sea in the western pacific, the South China Sea (SCS) receives large amount of terrigenous material annually through numerous rivers from surrounding continents and islands, which make it as the good place for the study of source to sink process. Yet few studies put emphasis on the northwestern continental shelf and slope in the SCS, even though most of the detrital materials derived from the Red River and Hainan Island are deposited in this area, and northwestern shelf plays a significant role in directly linking the South China, the Indochina and the South China Sea and thus controlling the source to sink process of terrestrial sediment. We presented the clay mineral and Sr-Nd isotopic composition of fine-grained fraction for sediments from northwestern SCS, in order to identify sediment source and transportation. The results show that the clay mineral of northwestern SCS sediments are mainly illite (30%~59%), smectite (20%~40%) and kaolinite (8%~35%), with minor chlorite. The illite chemical index varies between 0.19 and 0.75 with an average of 0.49, indicating an intensive hydrolysis in the source region. The 87Sr/86Sr ratios of sediments range from 0.716288 to 0.734416 (average of 0.724659), and ɛ Nd(0) values range from -10.31 to -11.62 (average of -10.93), which suggest that the source rocks of these sediments are derived from continental crust. The Hainan Island is an important source for sediments deposited in the nearshore and western shelf, especially for illite, kaolinite and smectite clay minerals. Furthermore, the relatively high contents of kaolinite and smectite in sediments from eastern shelf and southern slope of Hainan Island are also controlled by the supply of terrigenous materials from Hainan, which cannot be resulted from sedimentary differentiation of the Pearl and Red river sediments. And the correlation analysis

  8. Coupled S and Sr isotope evidences for elevated arsenic concentrations in groundwater from the world's largest antimony mine, Central China

    NASA Astrophysics Data System (ADS)

    Wen, Bing; Zhou, Aiguo; Zhou, Jianwei; Liu, Cunfu; Huang, Yuliu; Li, Ligang

    2018-02-01

    The Xikuangshan(XKS) mine, the world's largest antimony mine, was chosen for a detailed arsenic hydrogeochemical study because of the elevated arsenic in bedrock aquifers used by local residents. Hydrochemical data, δ34S values of dissolved SO42- and 87Sr/86Sr ratios have been analyzed to identify the predominant geochemical processes that control the arsenic mobilization within the aquifers. Groundwater samples can be divided into three major types: low arsenic groundwater (0-50 μg/L), high arsenic groundwater (50-1000 μg/L) and anomalous high arsenic groundwater (>1000 μg/L). Arsenic occurs under oxidizing conditions at the XKS Sb mine as the HAsO42- anion. The Ca/Na ratio correlates significantly with HCO3-/Na and Sr/Na ratios, indicating that carbonate dissolution and silicate weathering are the dominant processes controlling groundwater hydrochemistry. The δ34S values of the groundwater indicate that dissolved SO42- in groundwater is mainly sourced from the oxidation of sulfide minerals, and elevated As concentrations in groundwater are influenced by the mixing of mine water and surface water. Furthermore, the δ34S values are not correlated with dissolved As concentrations and Fe concentrations, suggesting that the reduction dissolution of Fe(III) hydroxides is not the dominant process controlling As mobilization. The 87Sr/86Sr ratios imply that elevated As concentrations in groundwater are primarily derived from the interaction with the stibnite and silicified limestone. More specifically, the excess-Na ion, the feature of Ca/Na ratio, and the spatial association of elevated As concentrations in groundwater collectively suggest that high and anomalous high arsenic groundwater are associated with smelting slags and, in particular, the arsenic alkali residue. In general, the hydrochemistry analysis, especially the S and Sr isotope evidences elucidate that elevated As concentrations and As mobilization are influenced by several geochemical processes

  9. Formation waters from Mississippian-Pennsylvanian reservoirs, Illinois basin, USA: Chemical and isotopic constraints on evolution and migration

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Stueber, A.M.; Walter, L.M.; Huston, T.J.

    1993-02-01

    We have analyzed a suite of seventy-four formation-water samples from Mississippian and Pennsylvanian carbonate and siliciclastic strata in the Illinois basin for major, minor, and trace element concentrations and for strontium isotopic composition. A subset of these samples was also analyzed for boron isotopic composition. Data are used to interpret origin of salinity and chemical and Sr isotopic evolution of the brines and in comparison with a similar data set from an earlier study of basin formation waters from Silurian-Devonian reservoirs. Systematics of Cl-Br-Na show that present Mississippian-Pennsylvanian brine salinity can be explained by a combination of subaerial seawater evaporationmore » short of halite saturation and subsurface dissolution of halite from an evaporite zone in the middle Mississippian St. Louis Limestone, along with extensive dilution by mixing with meteoric waters. Additional diagenetic modifications in the subsurface interpreted from cation/Br ratios include K depletion through interaction with clay minerals, Ca enrichment, and Mg depletion by dolomitization, and Sr enrichment through CaCO[sub 3] recrystallization and dolomitization. Ste. Genevieve Limestone (middle Mississippian) formation waters show [sup 87]Sr/[sup 86]Sr ratios in the range 0.70782-0.70900, whereas waters from the siliciclastic reservoirs are in the rante 0.70900-0.71052. Inverse correlations between [sup 87]Sr/[sup 86]Sr and B,Li, and Mg concentrations suggest that the brines acquired radiogenic [sup 87]Sr through interaction with siliciclastic minerals. Completely unsystematic relations between [sup 87]Fr/[sup 86]Sr and 1/Sr are observed; Sr concentrations in Ste. Genevieve and Aux Vases (middle Mississippian) waters appear to be buffered by equilibrium with respect to SrSo[sub 4]. These formation waters are distinguished from Silurian-Devonian brines in the basin by elevated Cl/Br and Na/Br ratios and by unsystematic Sr isotope relationships.« less

  10. Comparisons of multiple isotope systems in the aragonitic shells of cultured Arctica islandica clams

    NASA Astrophysics Data System (ADS)

    Liu, Y. W.; Aciego, S.; Wanamaker, A. D.

    2014-12-01

    Previous work using oxygen and stable carbon isotopes from Arctica islandica shells has shown that this archive can provide information on past seawater temperatures, carbon cycling and ocean circulation. However, relatively less attention has been devoted to other "non-traditional" isotope systems within this proxy archive. In this study, we report the boron (δ11B) and strontium isotopic values (87Sr/86Sr and δ88/86Sr) from A. islandicashells collected and cultured from the Gulf of Maine. The long-lived ocean quahog, A. islandica was collected and cultured in the Gulf of Maine for 8 months. Our high-resolution δ11B records from the experiment show 5-7‰ of increase through the culture, with low values from January to May and higher values after May. The 87Sr/86Sr ratios from both tank water and shell samples suggest that the shell material reflects ambient ocean chemistry without interferences from terrestrial sources. Although It has been suggested that stable Sr isotopic ratios (δ88/86Sr) in biogenic carbonates are influenced by the temperature of the precipitating fluid, our nearly identical δ88/86Sr data do not support this hypothesis despite a 15 °C temperature change during the experiment. Based on the in-situ measurements of culture seawater temperature, salinity and pH, and two commonly used fractionation factors (α3-4) for corals and forams, we predicted the range in shell δ11B values for the experiment. Our boron results are at the extreme ends of the two prediction lines suggesting the potential usage of the bivalve shells as seawater pH indicator. However, the wider range in δ11B in this experiment than the predictions based on other carbonate organisms (only 2 to 3‰) suggests that a species-specific fractionation factor may be required. Recent work from an additional constant temperature experiment (10 and 15 °C) in the Gulf of Maine will allow us to further evaluate temperature influences and potential vital effects on the shell boron

  11. Multiple sources for the origin of Late Jurassic Linglong adakitic granite in the Shandong Peninsula, eastern China: Zircon U-Pb geochronological, geochemical and Sr-Nd-Hf isotopic evidence

    NASA Astrophysics Data System (ADS)

    Ma, Liang; Jiang, Shao-Yong; Dai, Bao-Zhang; Jiang, Yao-Hui; Hou, Ming-Lan; Pu, Wei; Xu, Bin

    2013-03-01

    The Linglong granite is one of the most important Mesozoic plutons in the Shandong Peninsula, eastern China, and its petrogenesis has long been controversial, particularly with regard to the nature of source region and geodynamic setting. Our new precise zircon U-Pb dating results reveal that the Linglong granite was emplaced in the Late Jurassic (157-160 Ma). In addition, abundant inherited zircons are identified in the granite with four groups of age peaked at ~ 208, ~ 750, ~ 1800 and ~ 2450 Ma. Geochemical studies indicate that the Linglong granite is weakly peraluminous I-type granite, and is characterized by high SiO2, Sr and La, but low MgO, Y and Yb contents, strongly fractionated REE pattern and high Sr/Y and La/Yb ratios. It also exhibits high initial 87Sr/86Sr ratios (0.7097 to 0.7125), low ɛNd(t) (- 17.7 to - 20.3) and variable zircon ɛHf(t) (- 22.2 to - 8.7) values. Calculation of the zircon saturation temperature (TZr) reveals that the magma temperatures are 760 ± 20 °C, and the lowest TZr value of 740 °C may be close to initial magma temperature of this inheritance-rich rock. Interpretation of the elemental and isotopic data suggests that the Linglong granite has some affinities with the adakite, and was most likely derived from partial melting of thickened lower crust without any significant contribution of mantle components. The presence of a large number of inherited zircons and variable Sr-Nd-Hf isotopic compositions reveal that the Linglong granite probably has multiple sources consisting of the lower crust of both South China Block and North China Block, as well as the collision-related alkaline rocks and UHP metamorphic rocks. The continental arc-rifting related to the Izanagi plate subduction was the most likely geodynamic force for formation of the Jurassic Linglong adakatic granite in the Shandong Peninsula.

  12. Zinc isotope systematics of subduction-zone magmas

    NASA Astrophysics Data System (ADS)

    Huang, J.; Zhang, X. C.; Huang, F.; Yu, H.

    2016-12-01

    Subduction-zone magmas are generated by partial melting of mantle wedge triggered by addition of fluids derived from subducted hydrothermally altered oceanic lithosphere. Source of the fluids may be sediment, altered oceanic crust and serpentinized peridotite/serpentinite. Knowledge of the exact fluid source can facilitate our better understanding of the mechanism of fluid flux, element cycling and crust-mantle interaction in subduction zones. Zinc isotopes have the potential to place a constraint on this issue, because (1) Zn has an intermediate mobility during fluid-rock interaction and is enriched in subduction-zone fluids (e.g., Li et al., 2013); (2) sediment, altered oceanic crust and serpentinite have distinct Zn isotopic compositions (Pons et al., 2011); and (3) the mantle has a homogeneous Zn isotope composition (δ66Zn = 0.28 ± 0.05‰, Chen et al., 2013). Thus, the Zn isotopic composition of subduction-zone magmas reflects the characteristics of slab-derived fluids of different sources. Here, high-precision Zn isotope analyses were conducted on igneous rocks from arcs of Central America, Kamchatka, South Lesser Antilles, and Aleutian. One rhyolite with 75.1 wt.% SiO2 and 0.2 wt.% FeOT displays the heaviest δ66Zn value of 0.394‰ (relative to JMC Lyon) that probably results from the crystallization of Fe-Ti oxides during the late-stage differentiation. The rest of rocks have Zn isotopic compositions (0.161 to 0.339‰) similar to or lighter than those of the mantle. In an individual arc, the δ66Zn values of rocks show broad negative correlations with Ba/Th and 87Sr/86Sr ratios, suggesting that the slab-derived fluids should have lighter δ66Zn as well as higher Ba/Th and 87Sr/86Sr ratios relative to the mantle. These features are in accordance with those of serpentinites. Thus, addition of serpentinite-derived 66Zn-depleted fluids into the mantle wedge can explain the declined δ66Zn of subduction-zone magmas. ReferenceChen et al. (2013) EPSL 369

  13. Rapid and Accurate Behavioral Health Diagnostic Screening: Initial Validation Study of a Web-Based, Self-Report Tool (the SAGE-SR)

    PubMed Central

    Purcell, Susan E; Rhea, Karen; Maier, Philip; First, Michael; Zweede, Lisa; Sinisterra, Manuela; Nunn, M Brad; Austin, Marie-Paule; Brodey, Inger S

    2018-01-01

    Background The Structured Clinical Interview for DSM (SCID) is considered the gold standard assessment for accurate, reliable psychiatric diagnoses; however, because of its length, complexity, and training required, the SCID is rarely used outside of research. Objective This paper aims to describe the development and initial validation of a Web-based, self-report screening instrument (the Screening Assessment for Guiding Evaluation-Self-Report, SAGE-SR) based on the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) and the SCID-5-Clinician Version (CV) intended to make accurate, broad-based behavioral health diagnostic screening more accessible within clinical care. Methods First, study staff drafted approximately 1200 self-report items representing individual granular symptoms in the diagnostic criteria for the 8 primary SCID-CV modules. An expert panel iteratively reviewed, critiqued, and revised items. The resulting items were iteratively administered and revised through 3 rounds of cognitive interviewing with community mental health center participants. In the first 2 rounds, the SCID was also administered to participants to directly compare their Likert self-report and SCID responses. A second expert panel evaluated the final pool of items from cognitive interviewing and criteria in the DSM-5 to construct the SAGE-SR, a computerized adaptive instrument that uses branching logic from a screener section to administer appropriate follow-up questions to refine the differential diagnoses. The SAGE-SR was administered to healthy controls and outpatient mental health clinic clients to assess test duration and test-retest reliability. Cutoff scores for screening into follow-up diagnostic sections and criteria for inclusion of diagnoses in the differential diagnosis were evaluated. Results The expert panel reduced the initial 1200 test items to 664 items that panel members agreed collectively represented the SCID items from the 8 targeted

  14. FAST TRACK COMMUNICATION Accurate estimate of α variation and isotope shift parameters in Na and Mg+

    NASA Astrophysics Data System (ADS)

    Sahoo, B. K.

    2010-12-01

    We present accurate calculations of fine-structure constant variation coefficients and isotope shifts in Na and Mg+ using the relativistic coupled-cluster method. In our approach, we are able to discover the roles of various correlation effects explicitly to all orders in these calculations. Most of the results, especially for the excited states, are reported for the first time. It is possible to ascertain suitable anchor and probe lines for the studies of possible variation in the fine-structure constant by using the above results in the considered systems.

  15. Sr isotope evidence for a lacustrine origin for the upper Miocene to Pliocene Bouse Formation, lower Colorado River trough, and implications for timing of Colorado Plateau uplift

    USGS Publications Warehouse

    Spencer, J.E.; Patchett, P.J.

    1997-01-01

    The upper Miocene to Pliocene Bouse Formation in the lower Colorado River trough, which consists largely of siltstone with basal tufa and marl, has been interpreted as estuarine on the basis of paleontology. This interpretation requires abrupt marine inundation that has been linked to early rifting in the Gulf of California and Salton trough. New strontium isotope measurements reported here from carbonates and invertebrate shells in the Bouse Formation reveal no evidence of marine water, but are consistent with deposition in a lake or chain of lakes fed by the Colorado River. Furthermore, the absence of a southward decrease in 87Sr/86Sr within the Bouse Formation does not support the estuarine model in which low 87Sr/86Sr marine Sr would have dominated the mouth of the hypothetical Bouse estuary. Elevation of originally marine 87Sr/86Sr in the Bouse Formation to its present level, due to postdepositional interaction with ground water, is unlikely because Sr from secondary calcite above, below, and within the Bouse Formation is consistently less radiogenic, not more, than Bouse marl and shells. In contrast to Bouse Sr, strontium from mollusks in tidal-flat and delta-front paleoenvironments in the contemporaneous Imperial Formation in the Salton trough and from the subsurface south of Yuma was derived from sea water and confirms the dominance of marine strontium near or at the mouth of the late Miocene to early Pliocene Colorado River. Inferred post-early Pliocene uplift of the Bouse Formation from below sea level to modern elevations of up to 550 m has been used to support a late Cenozoic uplift age for the nearby Colorado Plateau. This constraint on uplift timing is eliminated if the Bouse Formation is lacustrine.

  16. Isotope hydrology of the Chalk River Laboratories site, Ontario, Canada

    USGS Publications Warehouse

    Peterman, Zell; Neymark, Leonid; King-Sharp, K.J.; Gascoyne, Mel

    2016-01-01

    This paper presents results of hydrochemical and isotopic analyses of groundwater (fracture water) and porewater, and physical property and water content measurements of bedrock core at the Chalk River Laboratories (CRL) site in Ontario. Density and water contents were determined and water-loss porosity values were calculated for core samples. Average and standard deviations of density and water-loss porosity of 50 core samples from four boreholes are 2.73 ± 12 g/cc and 1.32 ± 1.24 percent. Respective median values are 2.68 and 0.83 indicating a positive skewness in the distributions. Groundwater samples from four deep boreholes were analyzed for strontium (87Sr/86Sr) and uranium (234U/238U) isotope ratios. Oxygen and hydrogen isotope analyses and selected solute concentrations determined by CRL are included for comparison. Groundwater from borehole CRG-1 in a zone between approximately +60 and −240 m elevation is relatively depleted in δ18O and δ2H perhaps reflecting a slug of water recharged during colder climatic conditions. Porewater was extracted from core samples by centrifugation and analyzed for major dissolved ions and for strontium and uranium isotopes. On average, the extracted water contains 15 times larger concentration of solutes than the groundwater. 234U/238U and correlation of 87Sr/86Sr with Rb/Sr values indicate that the porewater may be substantially older than the groundwater. Results of this study show that the Precambrian gneisses at Chalk River are similar in physical properties and hydrochemical aspects to crystalline rocks being considered for the construction of nuclear waste repositories in other regions.

  17. Sr-87/Sr-86 isotopic age determination of upper Cretaceous Santonian, Campanian and Maastrichtian chondrichthyan teeth of the Atlantic and Eastern Gulf Coastal Plains: Implications for sea level cyclicity and macrofossil time-averaging in depositional sequence lag deposits

    NASA Astrophysics Data System (ADS)

    Becker, Martin Andrew

    1997-11-01

    Unconformities and fossil rich layers are common elements in the stratigraphic architecture of upper Cretaceous sediments exposed on both the Atlantic and Eastern Gulf Coastal Plains. Contacts between the Eutaw Formation and Tombigbee Sands Member in Alabama, the Blufftown Formation and Cusseta Sands in Georgia and the Wenonah- Mt. Laurel and Navesink Formations in New Jersey are marked by erosional surfaces with overlying blankets and lenses of macrofossil residuum. These contacts correspond to bounding unconformities and transgressive lags separating Santonian-Campanian, lower Campanian-upper Campanian and Campanian-Maastrichtian depositional sequences. Regression and subsequent transgression of sea level at the top of these depositional sequences resulted in hydrodynamic sorting of sediments and fossils that had previously accumulated in shelf and lower shoreface paleoenvironments. Remobilization of sediments by shoreface retreat reworked fossil hard-parts which became concentrated above erosional surfaces as sea level rose. Because of the abundance of chondrichthyan, pelecypod and ammonite fossils, these lags have great biostratigraphic significance and provide a basis for examining time averaging in macrofossil zonation. Chondrichthyan teeth are composed of extremely durable and highly insoluble, biogenic apatite. This tooth apatite accurately records the Sr87/Sr86 isotopic signature of seawater, from which the numerical age of the teeth can be calculated using published age/concentration data. Teeth (e.g. Squalicorax kaupi, Scapanorhynchus texanus) from Santonian-Campanian lag deposits at the contact of the Eutaw Formation and Tombigbee Sands Member in Alabama yield approximate ages of 85-81 Ma. Teeth from lower-upper Campanian lag deposits at the contact of the Blufftown Formation and Cusseta Sands in Georgia yield approximate ages of 83-75 Ma. Teeth from Campanian-Maastrichtian lag deposits at the contact of the Wenonah-Mt. Laurel and Navesink Formations in

  18. Use of Quantity Indicators for Forecasting of Biogeochemical Behavior Sr-90 and Cs-137 in the Conditions of the Combined Pollution of Soils

    NASA Astrophysics Data System (ADS)

    Lavrentyeva, G. V.; Geshel, I. V.

    2012-04-01

    From huge number of the radionuclides generated by anthropogenous activity the major value the group of biologically active radionuclides has. First of all, it Sr-90 and Cs-137 which play an important role in various radiological situations. In researches on studying of laws of behavior in environment Sr -90 and Cs-137 the basic attention was given to studying of influence of their chemical analogs Ca and K, instead of stable isotopes Sr and Cs. However, even low concentration of stable isotopes Sr and Cs in soil can influence on biogeochemical behavior of radionuclides. Objects of research: dernovo-podsolic soil, summer barley of grade, stable and radioactive isotopes Sr, Cs. Schemes of experiments provided entering of 8 doses stable Cs and Sr in the range from 0 to 500-750 mg/kg of air-dry weight of soil and 50 kBq of radionuclides on each frequency. Absorption of radionuclides by plants will be defined by two parametres of transport. The first - factor of transition (TF), which characterises level of regulation of process of carrying over of a radionuclide from soil in plants and depends on distribution of an element between the firm and liquid phase, distribution defined in the factor (Kd). The second parametre - factor of concentrating (CF) which characterises biological level of regulation of this process. The increase in quantity of stable Sr in soil leads to an active desorption Sr-90 in a soil solution on all frequency. Kd of Cs-137 on the general background of which decrease in values some increase in factor in the range of 120-225 mg of Cs/kg of soil is observed. Received Kd of radionuclides will well be co-ordinated with the revealed functional dependences between concentration Cs and Sr in soil and specific activity Cs-137 and Sr-90 in a soil solution. Comparison CF of two radionuclides shows that plants absorb Sr-90 from a soil solution actively, than Cs-137. Thus values CF of Sr-90 in the investigated interval of concentration of a stable isotope are

  19. Stages of weathering mantle formation from carbonate rocks in the light of rare earth elements (REE) and Sr-Nd-Pb isotopes

    NASA Astrophysics Data System (ADS)

    Hissler, Christophe; Stille, Peter

    2015-04-01

    Weathering mantles are widespread and include lateritic, sandy and kaolinite-rich saprolites and residuals of partially dissolved rocks. These old regolith systems have a complex history of formation and may present a polycyclic evolution due to successive geological and pedogenetic processes that affected the profile. Until now, only few studies highlighted the unusual high content of associated trace elements in weathering mantles originating from carbonate rocks, which have been poorly studied, compared to those developing on magmatic bedrocks. For instance, these enrichments can be up to five times the content of the underlying carbonate rocks. However, these studies also showed that the carbonate bedrock content only partially explains the soil enrichment for all the considered major and trace elements. Up to now, neither soil, nor saprolite formation has to our knowledge been geochemically elucidated. Therefore, the aim of this study was to examine more closely the soil forming dynamics and the relationship of the chemical soil composition to potential sources. REE distribution patterns and Sr-Nd-Pb isotope ratios have been used because they are particularly well suited to identify trace element migration, to recognize origin and mixing processes and, in addition, to decipher possible anthropogenic and/or "natural" atmosphere-derived contributions to the soil. Moreover, leaching experiments have been applied to identify mobile phases in the soil system and to yield information on the stability of trace elements and especially on their behaviour in these Fe-enriched carbonate systems. All these geochemical informations indicate that the cambisol developing on such a typical weathering mantle ("terra fusca") has been formed through weathering of a condensed Bajocian limestone-marl facies. This facies shows compared to average world carbonates important trace element enrichments. Their trace element distribution patterns are similar to those of the soil

  20. Isotopic constraints on contamination processes in the Tonian Goiás Stratiform Complex

    NASA Astrophysics Data System (ADS)

    Giovanardi, Tommaso; Mazzucchelli, Maurizio; Lugli, Federico; Girardi, Vicente A. V.; Correia, Ciro T.; Tassinari, Colombo C. G.; Cipriani, Anna

    2018-06-01

    The Tonian Goiás Stratiform Complex (TGSC, Goiás, central Brazil), is one of the largest mafic-ultramafic layered complexes in the world, emplaced during the geotectonic events that led to the Gondwana accretion. In this study, we present trace elements and in-situ U/Pb-Lu-Hf analyses of zircons and 87Sr/86Sr ratios of plagioclases from anorthosites and gabbros of the TGSC. Although formed by three isolated bodies (Cana Brava, Niquelândia and Barro Alto), and characterized by a Lower and Upper Sequence (LS and US), our new U/Pb zircon data confirm recent geochemical, geochronological, and structural evidences that the TGSC has originated from a single intrusive body in the Neoproterozoic. New Hf and Sr isotope ratios construe a complex contamination history for the TGSC, with different geochemical signatures in the two sequences. The low Hf and high Sr isotope ratios of the Lower Sequence (εHf(t) from -4.2 down to -27.5; 87Sr/86Sr = 0.706605-0.729226), suggest the presence of a crustal component and are consistent with contamination from meta-pelitic and calc-silicate rocks found as xenoliths within the Sequence. The more radiogenic Hf isotope ratios and low Sr isotope composition of the Upper Sequence (εHf(t) from 11.3 down to -8.4; 87Sr/86Sr = 0.702368-0.702452), suggest a contamination from mantle-derived metabasalts in agreement with the occurrences of amphibolite xenoliths in the US stratigraphy. The differential contamination of the two sequences is explained by the intrusion of the TGSC in a stratified crust dominated by metasedimentary rocks in its deeper part and metavolcanics at shallower levels. Moreover, the differential thermal gradient in the two crystallizing sequences might have contributed to the preservation and recrystallization of inherited zircon grains in the US and total dissolution or magmatic overgrowth of the LS zircons via melt/rock reaction processes.

  1. The evolution of a calc-alkaline basic to silicic magma system: Geochemical and Rb-Sr, Sm-Nd, and 18O /16O isotopic evidence from the Late Hercynian Atesina-Cima d'Asta volcano-plutonic complex, northern Italy

    NASA Astrophysics Data System (ADS)

    Barth, Susanne; Oberli, Felix; Meier, Martin; Blattner, Peter; Bargossi, Giuseppe M.; Di Battistini, Gianfranco

    1993-09-01

    Geochemical and Sr-Nd-O isotopic data presented for basaltic andesitic to rhyolitic and for quartz noritic to monzogranitic rock suites from the Late Hercynian calc-alkaline Atesina volcanic complex (AVC) and the Cima d'Asta pluton (CAP), Southern Alps (northern Italy), provide information on both the primary magmatic processes and the effects of (mainly Triassic) hydrothermal overprint. Fluid infiltration led to mobilization of major and trace elements (K 2O, Na 2O, CaO, Rb, Sr, and Ba), opensystem behavior in total-rock Rb-Sr, and shift in δ18O to elevated values (total rock up to 16.6%. and volcanic matrix up to 17.8%.). Oxygen isotopic disequilibrium between quartz-feldspar pairs suggests water-rock interaction at medium/low temperatures. The δ18O values of quartz, the REE characterized by regular LREE enrichment/HREE depletion, and the Sm-Nd isotopic signatures, however, remained virtually unaffected by secondary processes. The initial ɛNd values (at 270 Ma) of the AVC and CAP magmatites are restricted to overlapping ranges of -3.6 to -6.5 and of -2.7 to -6.5, respectively, indicating significant crustal contribution; these values and associated T DM model ages of 1.1-1.6 Ga agree well with those of typical South Alpine lower crustal magmatites. The AVC and CAP rocks do not follow the "normal" trend of increasingly crustal Nd isotopic signatures with progressive degree of magma evolution expected for a single-stage AFC-type process, but instead display an inversion of this relationship. Geochemical and isotopic constraints favor a model of a large-scale MASH-type melting and mixing zone at or near the base of the continental crust. Distinct elemental enrichment/depletion and REE crossover patterns displayed by high-silica as compared to less silicic AVC rhyolites suggest subsequent magma evolution within a shallow-level compositionally zoned chamber.

  2. Using 87Sr/86Sr ratios to investigate changes in stream chemistry during snowmelt in the Provo River, Utah, USA

    NASA Astrophysics Data System (ADS)

    Hale, C. A.; Carling, G. T.; Fernandez, D. P.; Nelson, S.; Aanderud, Z.; Tingey, D. G.; Dastrup, D.

    2017-12-01

    Water chemistry in mountain streams is variable during spring snowmelt as shallow groundwater flow paths are activated in the watershed, introducing solutes derived from soil water. Sr isotopes and other tracers can be used to differentiate waters that have interacted with soils and dust (shallow groundwater) and bedrock (deep groundwater). To investigate processes controlling water chemistry during snowmelt, we analyzed 87Sr/86Sr ratios, Sr and other trace element concentrations in bulk snowpack, dust, soil, soil water, ephemeral channels, and river water during snowmelt runoff in the upper Provo River watershed in northern Utah, USA, over four years (2014-2017). Strontium concentrations in the river averaged 20 ppb during base flow and decreased to 10 ppb during snowmelt runoff. 87Sr/86Sr ratios were around 0.717 during base flow and decreased to 0.715 in 2014 and 0.713 in 2015 and 2016 during snowmelt, trending towards less radiogenic values of mineral dust inputs in the Uinta Mountain soils. Ephemeral channels, representing shallow flow paths with soil water inputs, had Sr concentrations between 7-20 ppb and 87Sr/86Sr ratios between 0.713-0.716. Snowpack Sr concentrations were generally <2 ppb with 87Sr/86Sr ratios between 0.710-711, similar to atmospheric dust inputs. The less radiogenic 87Sr/86Sr ratios and lower Sr concentrations in the river during snowmelt are likely a result of activating shallow groundwater flow paths, which allows melt water to interact with shallow soils that contain accumulated dust deposits with a less radiogenic 87Sr/86Sr ratio. These results suggest that flow paths and atmospheric dust are important to consider when investigating variable solute loads in mountain streams.

  3. Rb-Sr And Sm-Nd Ages, and Petrogenesis of Depleted Shergottite Northwest Africa 5990

    NASA Technical Reports Server (NTRS)

    Shih, C. Y.; Nyquist, L. E.; Reese, Y.; Irving, A. J.

    2011-01-01

    Northwest Africa (NWA) 5990 is a very fresh Martian meteorite recently found on Hamada du Draa, Morocco and was classified as an olivine-bearing diabasic igneous rock related to depleted shergottites [1]. The study of [1] also showed that NWA 5990 resembles QUE 94201 in chemical, textural and isotopic aspects, except QUE 94201 contains no olivine. The depleted shergottites are characterized by REE patterns that are highly depleted in LREE, older Sm-Nd ages of 327-575 Ma and highly LREE-depleted sources with Nd= +35+48 [2-7]. Age-dating these samples by Sm-Nd and Rb-Sr methods is very challenging because they have been strongly shocked and contain very low abundances of light rare earth elements (Sm and Nd), Rb and Sr. In addition, terrestrial contaminants which are commonly present in desert meteorites will compromise the equilibrium of isotopic systems. Since NWA 5990 is a very fresh meteorite, it probably has not been subject to significant desert weathering and thus is a good sample for isotopic studies. In this report, we present Rb-Sr and Sm-Nd isotopic results for NWA 5990, discuss the correlation of the determined ages with those of other depleted shergottites, especially QUE 94201, and discuss the petrogenesis of depleted shergottites.

  4. 40Ar/39Ar ages and Sr-Nd-Pb isotopic compositions of alkaline and tholeiitic rocks from the northern Deccan Traps

    NASA Astrophysics Data System (ADS)

    Marzoli, A.; Parisio, L.; Jourdan, F.; Melluso, L.; Sethna, S. F.; Bellieni, G.

    2015-12-01

    The Deccan large igneous province in India was emplaced close to the Cretaceous-Paleogene boundary (K-Pg; 66.0 Ma) and is formed by tholeiitic and alkaline rocks. Definition of the origin of Deccan magmatism and of its environmental impact relies on precise and accurate geochronological analyses. We present new 40Ar/39Ar ages from the northern sector of the province. In this area, tholeiitic and alkaline rocks were contemporaneously emplaced at 66.60±0.35 to 65.25±0.29 Ma in the Phenai Mata area, while rocks from Rajpipla and Mt. Pavagadh yielded ages ranging from 66.40±2.80 to 64.90±0.80 Ma. Indistinguishable ages for alkaline and tholeiitic magmatism, coupled with distinct major and trace element and Sr-Nd-Pb isotopic compositions suggest that distinct mantle sources, necessary for the two magmatic series were synchronously active. The new ages are compared with previous ages, which were carefully screened and filtered and then recalculated in order to be comparable. The entire data set of geochronological data does not support a time-related migration of the magmatism related to the northward Indian Plate movement relative to the Reunion mantle plume. The main phase of magmatism, including the newly dated rocks from the Northern Deccan occurred across the K-Pg boundary, confirming a causal link between the emplacement of the province and the K-Pg mass extinction.

  5. Radiogenic Isotopes in Weathering and Hydrology

    NASA Astrophysics Data System (ADS)

    Blum, J. D.; Erel, Y.

    2003-12-01

    as on the observation that radiogenic isotopes are sometimes preferentially released compared to nonradiogenic isotopes of the same element during acid leaching of rocks ( Hart and Tilton, 1966; Silver et al., 1984; Erel et al., 1991). A major finding of these investigations was that weathering often results in anomalously young Rb-Sr isochron ages, and discordant Pb-Pb ages. Rubidium is generally retained relative to strontium in whole-rock samples, and in some cases radiogenic strontium and lead are lost preferentially to common strontium and lead from weathered minerals.The most widely utilized of these isotopic systems is Rb-Sr, followed by U-Pb. The K-Ar system is not directly applicable to most studies of rock-water interaction, because argon is a noble gas, and upon release during mineral weathering mixes with atmospheric argon, limiting its usefulness as a tracer in most weathering applications. Argon and other noble gas isotopes have, however, found important applications in hydrology (see Chapter 5.15). Three other isotopic systems commonly used in geochronology and petrology include Sm-Nd, Lu-Hf, and Re-Os. These parent and daughter elements are in very low abundance and concentrated in trace mineral phases. Sm-Nd, Lu-Hf, and Re-Os have been used in a few weathering studies but have not been utilized extensively in investigations of weathering and hydrology.The decay of 87Rb to 87Sr has a half-life of 48.8 Gyr, and this radioactive decay results in natural variability in the 87Sr/86Sr ratio in rubidium-bearing minerals (e.g., Blum, 1995). The trace elements rubidium and strontium are geochemically similar to the major elements potassium and calcium, respectively. Therefore, minerals with high K/Ca ratios develop high 87Sr/86Sr ratios over geologic timescales. Once released into the hydrosphere, strontium retains its isotopic composition without significant fractionation by geochemical or biological processes, and is therefore a good tracer for sources and

  6. Neodymium and strontium isotopic study of Australasian tektites - New constraints on the provenance and age of target materials

    NASA Technical Reports Server (NTRS)

    Blum, Joel D.; Papanastassiou, D. A.; Wasserburg, G. J.; Koeberl, C.

    1992-01-01

    The Nd and Sr isotopic compositions of Australasian tectites (including two flanged Australian tectites, two low-SiO2 Muong Nong-type tectites, and three high-SiO2 Muong Nong-type tectites) and the Nd, Sm, Sr, and Rb concentrations were investigated by isotope-dilution thermal ionization mass spectrometry, and the Sm-Nd and Rb-Sr isotope systematics were used to study the characteristics of the parental material. It is shown that the Nd and Sr isotopic data provide evidence that all Australasian tektites were derived from a single sedimentary formation with a narrow range of stratigraphic ages close to 170 Ma. It is suggested that all of the Australasian tektites were derived from a single impact event and that the australites represent the upper part of a melt sheet ejected at high velocity, whereas the indochinites represent melts formed at a lower level in the target material distributed closer to the area of the impact.

  7. Pb isotope compositions of modern deep sea turbidites

    NASA Astrophysics Data System (ADS)

    Hemming, S. R.; McLennan, S. M.

    2001-01-01

    Modern deep sea turbidite muds and sands collected from Lamont piston cores represent a large range in age of detrital sources as well as a spectrum of tectonic settings. Pb isotope compositions of all but three of the 66 samples lie to the right of the 4.56 Ga Geochron, and most also lie along a slope consistent with a time-integrated κ ( 232Th/ 238U) between 3.8 and 4.2. Modern deep sea turbidites show a predictable negative correlation between both Pb and Sr isotope ratios and ɛNd and ɛHf, clearly related to the age of continental sources. However, the consistency between Pb and Nd isotopes breaks down for samples with very old provenance ( ɛNd<-20) that are far less radiogenic than predicted by the negative correlation. The correlations among Sr, Nd and Hf isotopes also become more scattered in samples with very old provenance. The unradiogenic Pb isotopic character of modern sediments with Archean Nd model ages is consistent with a model where Th and U abundances of the Archean upper crust are significantly lower than the post-Archean upper crust.

  8. U-Pb zircon, geochemical and Sr-Nd-Hf-O isotopic constraints on age and origin of the ore-bearing intrusions from the Nurkazgan porphyry Cu-Au deposit in Kazakhstan

    NASA Astrophysics Data System (ADS)

    Shen, Ping; Pan, Hongdi; Seitmuratova, Eleonora; Jakupova, Sholpan

    2016-02-01

    Nurkazgan, located in northeastern Kazakhstan, is a super-large porphyry Cu-Au deposit with 3.9 Mt metal copper and 229 tonnage gold. We report in situ zircon U-Pb age and Hf-O isotope data, whole rock geochemical and Sr-Nd isotopic data for the ore-bearing intrusions from the Nurkazgan deposit. The ore-bearing intrusions include the granodiorite porphyry, quartz diorite porphyry, quartz diorite, and diorite. Secondary ion mass spectrometry (SIMS) zircon U-Pb dating indicates that the granodiorite porphyry and quartz diorite porphyry emplaced at 440 ± 3 Ma and 437 ± 3 Ma, respectively. All host rocks have low initial 87Sr/86Sr ratios (0.70338-0.70439), high whole-rock εNd(t) values (+5.9 to +6.3) and very high zircon εHf(t) values (+13.4 to +16.5), young whole-rock Nd and zircon Hf model ages, and consistent and slightly high zircon O values (+5.7 to +6.7), indicating that the ore-bearing magmas derived from the mantle without old continental crust involvement and without marked sediment contamination during magma emplacement. The granodiorite porphyry and quartz diorite porphyry are enriched in large ion lithophile elements (LILE) and light rare earth elements (LREE) and depleted in high-field strength elements (HFSE), Eu, Ba, Nb, Sr, P and Ti. The diorite and quartz diorite have also LILE and LREE enrichment and HFSE, Nb and Ti depletion, but have not negative Eu, Ba, Sr, and P anomalies. These features suggest that the parental magma of the granodiorite porphyry and quartz diorite porphyry originated from melting of a lithospheric mantle and experienced fractional crystallization, whereas the diorite and quartz diorite has a relatively deeper lithospheric mantle source region and has not experienced strong fractional crystallization. Based on these, together with the coeval ophiolites in the area, we propose that a subduction of the Balkhash-Junggar oceanic plate took place during the Early Silurian and the ore-bearing intrusions and associated Nurkazgan

  9. Isotopic and Chemical Evidence for Primitive Aqueous Alteration in the Tagish Lake Meteorite

    NASA Astrophysics Data System (ADS)

    Sakuma, Keisuke; Hidaka, Hiroshi; Yoneda, Shigekazu

    2018-01-01

    Aqueous alteration is one of the primitive activities that occurred on meteorite parent bodies in the early solar system. The Tagish Lake meteorite is known to show an intense parent body aqueous alteration signature. In this study, quantitative analyses of the alkaline elements and isotopic analyses of Sr and Ba from acid leachates of TL (C2-ungrouped) were performed to investigate effects of aqueous alteration. The main purpose of this study is to search for isotopic evidence of extinct 135Cs from the Ba isotopic analyses in the chemical separates from the Tagish Lake meteorite. Barium isotopic data from the leachates show variable 135Ba isotopic anomalies (ε = ‑2.6 ∼ +3.6) which correlatewith 137Ba and 138Ba suggesting a heterogeneous distribution of s- and r-rich nucleosynthetic components in the early solar system. The 87Rb–87Sr and 135Cs–135Ba decay systems on TL in this study do not provide any chronological information. The disturbance of the TL chronometers is likely a reflection of the selective dissolution of Cs and Rb given the relatively higher mobility of Cs and Rb compared to Ba and Sr, respectively, during fluid mineral interactions.

  10. Improving 14C dating precision in dynamic, brackish waters by one order of magnitude: 87Sr/86Sr isotopes as a quantitative proxy for 14C reservoir age.

    NASA Astrophysics Data System (ADS)

    Lougheed, B.; Davies, G.; Filipsson, H. L.; van der Lubbe, J.; Snowball, I.

    2016-12-01

    Accurate geochronologies are crucial for reconstructing the sensitivity of brackish and estuarine environments to external impacts. A common geochronological method used for such studies is radiocarbon (14C) dating, but its application in brackish environments is severely limited by an inability to quantify spatiotemporal variations in 14C reservoir age, or R(t), due to dynamic interplay between river runoff and marine water in these environments. Additionally, old carbon effects and species-specific behavioural processes also influence 14C ages. Using the world's largest brackish water body (the estuarine Baltic Sea) as a test-bed, combined with a comprehensive approach that objectively excludes both old carbon and species-specific effects, we demonstrate that it is possible to use 87Sr/86Sr ratios to quantify R(t) in ubiquitous mollusc shell material, leading to an almost one order of magnitude increase in Baltic Sea 14C geochronological precision over the current state-of-the-art. We propose that this novel proxy method can be developed for other brackish water bodies worldwide, thereby improving geochronological control in these climate sensitive, near-coastal environments.

  11. Sr heterogeneity in textit{Arctica islandica} shells and the potential use of Sr/Ca ratios as paleotemperature proxies

    NASA Astrophysics Data System (ADS)

    Radermacher, Pascal; Schöne, Bernd R.; Nunn, Elizabeth V.; Zengjie, Zhang

    2010-05-01

    Quantifiable paleotemperature data can help to verify predictions made by numerical climate models. Traditionally, paleotemperature estimates are based on δ18O values of biogenic hard parts. However, oxygen isotope values not only reflect changes in ambient temperature, but also changes in δ18Owater, i.e. driven by freshwater influx, evaporation etc. Information regarding the δ18Owater value of past environments is limited for the geological past. The validity of published δ18O paleotemperature data can be tested using element-to-calcium ratios of bivalve shells such as the long-lived ocean quahog, Arctica islandica. Preliminary investigations suggest that Sr/Ca ratios of this species may provide more reliable paleotemperature data. However, contemporaneously deposited shell portions within the outer shell layer demonstrate at least a 30% variability in the Sr/Ca value. This study presents Sr/Ca ratios measured by ICP-OES wet-chemical analyses. Significantly different distributions of Sr/Ca ratios were recorded from the shell surface (over 1330 ppm), through the interior (850 ppm) and to the inner shell surface (1860 ppm). Furthermore, this study showed that different shell crystal fabrics incorporate different amounts of Sr into the CaCO3 lattice of the A. islandica shell. Disparate Sr distribution could potentially be explained either by postdepositional diagenetic processes or syndepositional processes during biomineralization (i.e. different amounts of Sr incorporated into the shell). Understanding the mechanism of the observed Sr heterogeneity is essential if Sr/Ca ratios are to be used confidently in paleotemperature reconstructions.

  12. Parental Sources of High-Alumina Alkaline Melts: Nd, Sr, Pb, and O Isotopic Evidence from the Devonian Kiya-Shaltyr Gabbro-Urtite Intrusion, South Siberia

    NASA Astrophysics Data System (ADS)

    Vrublevskii, V. V.; Gertner, I. F.; Chugaev, A. V.

    2018-04-01

    The isotope geochemistry (ɛNd( t) 4.8-5.4, 206Pb/204Pb in 18.05-18.36, 207Pb/204Pbin 15.53-15.57, 208Pb/204Pb in 37.59-37.83, 87Sr/86Sr( t) 0.7048-0.7057, δ18OSMOW 8-10.5‰) and trace element composition of the Kiya-Shaltyr gabbro-urtite pluton allow us to suggest a heterogeneous source and complex geodynamic settings of the Devonian alkali magmatism in the Kuznetsk Alatau. It is assumed that its evolution took place under conditions of partial mingling of matter of the depleted (PREMA) and enriched (EM) mantle with crustal contamination of the evolving melt. Such an interaction could have been a result of superposition of a mantle plume and an active margin (OIB and IAB components). In fold belts this led to the formation of hybrid high-alumina foidoite magmas.

  13. Reinterpreting the Early Cretaceous Sulfur Isotope Records: Implications for the Evolution of Seawater Chemistry

    NASA Astrophysics Data System (ADS)

    Mills, J. V.; Gomes, M. L.; Sageman, B. B.; Jacobson, A. D.; Hurtgen, M. T.

    2013-12-01

    The geologic record of the Cretaceous is punctuated by several periods of high organic carbon burial interpreted to represent global Ocean Anoxic Events (OAEs). In addition to the short-term (<1-Myr) changes in carbon (C) cycling associated with OAEs, evidence from a number of geochemical proxies has been interpreted to represent large-scale changes in ocean chemistry during the period. Specifically, the sulfur (S) isotope composition of early Cretaceous seawater sulfate as recorded in marine barite exhibits an ~5 permil shift in d34Ssulfate that persists for ~15Myr before returning to pre-excursion values. Superimposed upon this long-term shift in S-isotopes is OAE1a, the second major anoxic event recognized in the Cretaceous. Two hypotheses have been proposed to explain this S isotope perturbation: (1) massive evaporite deposition associated with rifting during the opening of the South Atlantic and a corresponding decrease in pyrite burial rates and (2) increased inputs of volcanic-derived S due to extensive LIP-volcanism. While there is geologic evidence for both evaporite deposition and enhanced hydrothermal activity, the relative influence of these potential driving factors remains largely unconstrained. Variation in the strontium (Sr) isotope composition of marine carbonates provides a tool for distinguishing between these influences. We examine the S isotope composition of carbonate-associated sulfate (CAS) spanning the Barremian through Aptian from Resolution Guyot (ODP Site 866) and compare the S isotope record to time equivalent records of carbon and strontium isotopes. Correlative changes in the C, S, and Sr cycles are observed: an ~5 permil shift in d34Ssulfate, which begins at the onset of OAE1a and continues after the positive d13Ccarb excursion, is accompanied by a contemporaneous, parallel shift in 87Sr/86Sr to unradiogenic values. The tight coupling observed between S and Sr throughout the interval is highly suggestive of a common driving mechanism

  14. K isotopes as a tracer of seafloor hydrothermal alteration

    NASA Astrophysics Data System (ADS)

    Parendo, Christopher A.; Jacobsen, Stein B.; Wang, Kun

    2017-02-01

    At ocean spreading ridges, circulation of seawater through rock at elevated temperatures alters the chemical and isotopic composition of oceanic crust. Samples obtained from drilling into ocean floor and from ophiolites have demonstrated that certain isotope systems, such as 18O/16O and 87Sr/86Sr, are systematically modified in hydrothermally altered oceanic crust. Although K is known to be mobile during hydrothermal alteration, there have not yet been any K-isotope analyses of altered oceanic crustal materials. Moreover, the 41K/39K of seawater was recently found to be significantly higher than that of igneous rocks, so the addition of seawater K to oceanic crust would be expected to generate 41K/39K variations in affected rocks. Here, we report high-precision 41K/39K measurements for samples from the Bay of Islands ophiolite, and we document large variations in 41K/39K, covarying with previous determinations of 87Sr/86Sr. Our data indicate that analytically resolvable 41K/39K effects arise in oceanic crust as a result of hydrothermal alteration. This finding raises the possibility that 41K/39K can be used as an effective tracer of oceanic crust recycled into the mantle, as a diagnostic criterion by which to identify ancient fragments of oceanic crust, and as a constraint on the flux of K between oceanic crust and seawater.

  15. Isotopic constraints on the age and early differentiation of the Earth.

    PubMed

    McCulloch, M T

    1996-03-01

    The Earth's age and early differentiation history are re-evaluated using updated isotopic constraints. From the most primitive terrestrial Pb isotopic compositions found at Isua Greenland, and the Pilbara of Western Australia, combined with precise geochronology of these localities, an age 4.49 +/- 0.02 Ga is obtained. This is interpreted as the mean age of core formation as U/Pb is fractionated due to sequestering of Pb into the Earth's core. The long-lived Rb-Sr isotopic system provides constraints on the time interval for the accretion of the Earth as Rb underwent significant depletion by volatile loss during accretion of the Earth or its precursor planetesimals. A primitive measured 87Sr/86Sr initial ratio of 0.700502 +/- 10 has been obtained for an early Archean (3.46 Ga) barite from the Pilbara Block of Western Australia. Using conservative models for the evolution of Rb/Sr in the early Archean mantle allows an estimate to be placed on the Earth's initial Sr ratio at approximately 4.50 Ga, of 0.69940 +/- 10. This is significantly higher than that measured for the Moon (0.69900 +/- 2) or in the achondrite, Angra dos Reis (0.69894 +/- 2) and for a Rb/Sr ratio of approximately 1/2 of chondrites corresponds to a mean age for accretion of the Earth of 4.48 + /- 0.04 Ga. The now extinct 146Sm-142Nd (T1/2(146)=103 l0(6)yrs) combined with the long-lived 147Sm-143Nd isotopic systematics can also be used to provide limits on the time of early differentiation of the Earth. High precision analyses of the oldest (3.8-3.9 Ga) Archean gneisses from Greenland (Amitsoq and Akilia gneisses), and Canada (Acasta gneiss) do not show measurable (> +/- l0ppm) variations of 142Nd, in contrast to the 33 ppm 142Nd excess reported for an Archean sample. The general lack of 142Nd variations, combined with the presence of highly positive epsilon 143 values (+4.0) at 3.9 Ga, indicates that the record of large-scale Sm/Nd fractionation events was not preserved in the early-Earth from 4

  16. Stable isotopes, Sr/Ca, and Mg/Ca in biogenic carbonates from Petaluma Marsh, northern California, USA

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Ingram, B.L.; De Deckker, P.; Chivas, A.R.

    2004-10-19

    Stable isotope ({sup 18}O/{sup 16}O and {sup 13}C/{sup 12}C) and minor-element compositions (Sr/Ca and Mg/Ca ratios) of ostracodes and gastropods separated from marsh sediments from San Francisco Bay, Northern California, were used to reconstruct paleoenvironmental changes in Petaluma Marsh over the past 700 yr. The value of {delta}{sup 18}O in the marsh carbonates reflects changes in freshwater inflow, evaporation, and temperature. Mg/Ca and Sr/Ca in ostracode calcite reflect changes in both freshwater inflow and temperature, although primarily reflect temperature changes in the salinity range of about 10-35 {per_thousand}. Ostracode {delta}{sup 18}O values show a gradual increase by 5 {per_thousand} betweenmore » 500 yr BR and the present, probably reflecting rising sea level and increased evaporation in the marsh. Superimposed on this trend are higher frequency Mg/Ca and {delta}{sup 18}O variations (3-4 {per_thousand}), probably reflecting changes in freshwater inflow and evaporation. A period of low Mg/Ca occurred between about 100-300 cal yr BP, suggesting wetter and cooler conditions during the Little Ice Age. Higher Mg/Ca ratios occurred 600-700 cal yr BP, indicating drier and warmer conditions during the end of the Medieval Warm Period. Both ostracode and gastropod {delta}{sup 13}C values decrease up-core, reflecting decomposition of marsh vegetation, which changes from C{sub 4} ({delta}{sup 13}C {approx} -12{per_thousand}) to CAM ({delta}{sup 13}C = -26 {per_thousand})-type vegetation over time.« less

  17. Stable isotopes, Sr/Ca, and Mg/Ca in biogenic carbonates from Petaluma Marsh, northern California, USA

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Ingram, B.L.; Deckker, P. de; Chivas, A.R.

    1998-10-01

    Stable isotope ({sup 18}O/{sup 16}O and {sup 13}C/{sup 12}C) and minor-element compositions (Sr/Ca and Mg/Ca ratios) of ostracodes and gastropods separated from marsh sediments from San Francisco Bay, Northern California, were used to reconstruct paleoenvironmental changes in Petaluma March over the past 700 yr. The value of {delta}{sup 18}O in the marsh carbonates reflects changes in freshwater inflow, evaporation, and temperature. Mg/Ca and Sr/Ca in ostracode calcite reflect changes in both freshwater inflow and temperature, although primarily reflect temperature changes in the salinity range of about 10--35{per_thousand}. Ostracode {delta}{sup 18}O values show a gradual increase by 5{per_thousand} between 500 yrmore » BP and the present, probably reflecting rising sea level and increased evaporation in the marsh. Superimposed on this trend are higher frequency Mg/Ca and {delta}{sup 18}O variations (3--4{per_thousand}), probably reflecting changes in freshwater inflow and evaporation. A period of low Mg/Ca occurred between about 100--300 cal yr BP, suggesting wetter and cooler conditions during the Little Ice Age. Higher Mg/Ca ratios occurred 600--700 cal yr BP, indicating drier and warmer conditions during the end of the Medieval Warm Period. Both ostracode and gastropod {delta}{sup 13}C values decrease up-core, reflecting decomposition of marsh vegetation, which changes from C{sub 4} ({delta}{sup 13}C {approximately} {minus}12{per_thousand}) to CAM ({delta}{sup 13}C = {minus}26{per_thousand})-type vegetation over time.« less

  18. Persistence of fertile and hydrous lithospheric mantle beneath the northwestern Ethiopian plateau: Evidence from modal, trace element and Sr-Nd-Hf isotopic compositions of amphibole-bearing mantle xenoliths

    NASA Astrophysics Data System (ADS)

    Alemayehu, Melesse; Zhang, Hong-Fu; Aulbach, Sonja

    2017-07-01

    We present new trace element compositions of amphiboles, Sr-Nd-Hf isotope compositions of clinopyroxenes and mineral modes for spinel peridotite xenoliths that were entrained in a Miocene alkali basalt (Gundeweyn, northwestern Ethiopian plateau), in order to understand the geochemical evolution and variation occurring within the continental lithospheric mantle (CLM) in close proximity to the East African Rift system, and its dynamic implications. With the exception of a single amphibole-bearing sample that is depleted in LREE (La/YbN = 0.45 × Cl), amphiboles in lherzolites and in one harzburgite show variable degrees of LREE enrichment (La/YbN = 2.5-12.1 × Cl) with flat HREE (Dy/YbN = 1.5-2.1 × Cl). Lherzolitic clinoyroxenes have 87Sr/86Sr (0.70227 to 0.70357), 143Nd/144Nd (0.51285 to 0.51346), and 176Hf/177Hf (0.28297 to 0.28360) ranging between depleted lithosphere and enriched mantle. LREE-enriched clinopyroxenes generally have more enriched isotope compositions than depleted ones. While lherzolites with isotope compositions similar to those of the Afar plume result from the most recent metasomatic overprint, isotope compositions more depleted than present-day MORB can be explained by an older melt extraction and/or isotopic rehomogenisation event, possibly related to the Pan-African orogeny. Several generations of amphibole are recognized in accord with this multi-stage evolution. Texturally unequilibrated amphibole occurring within the peridotite matrix and in melt pockets attest to continued hydration and refertilization of the lithospheric mantle subsequent to Oligocene flood basalt magmatism, during which an earlier-emplaced inventory of amphibole was likely largely consumed. However, a single harzburgite contains amphibole with the highest Mg# and lowest TiO2 content, which is interpreted as sampling a volumetrically subordinate mantle region beneath the Ethiopian plateau that was not tapped during flood basalt magmatism. Strikingly, both trace

  19. High-precision isotopic characterization of USGS reference materials by TIMS and MC-ICP-MS

    NASA Astrophysics Data System (ADS)

    Weis, Dominique; Kieffer, Bruno; Maerschalk, Claude; Barling, Jane; de Jong, Jeroen; Williams, Gwen A.; Hanano, Diane; Pretorius, Wilma; Mattielli, Nadine; Scoates, James S.; Goolaerts, Arnaud; Friedman, Richard M.; Mahoney, J. Brian

    2006-08-01

    The Pacific Centre for Isotopic and Geochemical Research (PCIGR) at the University of British Columbia has undertaken a systematic analysis of the isotopic (Sr, Nd, and Pb) compositions and concentrations of a broad compositional range of U.S. Geological Survey (USGS) reference materials, including basalt (BCR-1, 2; BHVO-1, 2), andesite (AGV-1, 2), rhyolite (RGM-1, 2), syenite (STM-1, 2), granodiorite (GSP-2), and granite (G-2, 3). USGS rock reference materials are geochemically well characterized, but there is neither a systematic methodology nor a database for radiogenic isotopic compositions, even for the widely used BCR-1. This investigation represents the first comprehensive, systematic analysis of the isotopic composition and concentration of USGS reference materials and provides an important database for the isotopic community. In addition, the range of equipment at the PCIGR, including a Nu Instruments Plasma MC-ICP-MS, a Thermo Finnigan Triton TIMS, and a Thermo Finnigan Element2 HR-ICP-MS, permits an assessment and comparison of the precision and accuracy of isotopic analyses determined by both the TIMS and MC-ICP-MS methods (e.g., Nd isotopic compositions). For each of the reference materials, 5 to 10 complete replicate analyses provide coherent isotopic results, all with external precision below 30 ppm (2 SD) for Sr and Nd isotopic compositions (27 and 24 ppm for TIMS and MC-ICP-MS, respectively). Our results also show that the first- and second-generation USGS reference materials have homogeneous Sr and Nd isotopic compositions. Nd isotopic compositions by MC-ICP-MS and TIMS agree to within 15 ppm for all reference materials. Interlaboratory MC-ICP-MS comparisons show excellent agreement for Pb isotopic compositions; however, the reproducibility is not as good as for Sr and Nd. A careful, sequential leaching experiment of three first- and second-generation reference materials (BCR, BHVO, AGV) indicates that the heterogeneity in Pb isotopic compositions

  20. Rapid and Accurate Behavioral Health Diagnostic Screening: Initial Validation Study of a Web-Based, Self-Report Tool (the SAGE-SR).

    PubMed

    Brodey, Benjamin; Purcell, Susan E; Rhea, Karen; Maier, Philip; First, Michael; Zweede, Lisa; Sinisterra, Manuela; Nunn, M Brad; Austin, Marie-Paule; Brodey, Inger S

    2018-03-23

    The Structured Clinical Interview for DSM (SCID) is considered the gold standard assessment for accurate, reliable psychiatric diagnoses; however, because of its length, complexity, and training required, the SCID is rarely used outside of research. This paper aims to describe the development and initial validation of a Web-based, self-report screening instrument (the Screening Assessment for Guiding Evaluation-Self-Report, SAGE-SR) based on the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) and the SCID-5-Clinician Version (CV) intended to make accurate, broad-based behavioral health diagnostic screening more accessible within clinical care. First, study staff drafted approximately 1200 self-report items representing individual granular symptoms in the diagnostic criteria for the 8 primary SCID-CV modules. An expert panel iteratively reviewed, critiqued, and revised items. The resulting items were iteratively administered and revised through 3 rounds of cognitive interviewing with community mental health center participants. In the first 2 rounds, the SCID was also administered to participants to directly compare their Likert self-report and SCID responses. A second expert panel evaluated the final pool of items from cognitive interviewing and criteria in the DSM-5 to construct the SAGE-SR, a computerized adaptive instrument that uses branching logic from a screener section to administer appropriate follow-up questions to refine the differential diagnoses. The SAGE-SR was administered to healthy controls and outpatient mental health clinic clients to assess test duration and test-retest reliability. Cutoff scores for screening into follow-up diagnostic sections and criteria for inclusion of diagnoses in the differential diagnosis were evaluated. The expert panel reduced the initial 1200 test items to 664 items that panel members agreed collectively represented the SCID items from the 8 targeted modules and DSM criteria for the covered

  1. The Incredible, Embryological Egg: Calcium and Strontium Isotopes Recapitulate Ontogeny

    NASA Astrophysics Data System (ADS)

    Gordon, G. W.; Skulan, J. L.

    2011-12-01

    Embryological development reflects evolutionary history. Understanding the processes of fetal growth is important for curing human birth defects and predicting damage to ecosystems from environmental insults. Tracing enzymatic and hormonal gradients during development, and correlating them to genetic cues dominate modern embryology. Previous work done tracing the mass transfer of elements has generally been limited to isotope spikes in vitro. Natural mass-dependent Ca and Sr isotopic ratios and radiogenic Sr isotopes have the potential to reveal both source and biochemical mechanism information about processes in vivo, but have not previously been extensively explored. The process when a hen lays a fertilized egg that becomes a chick includes formation and dissolution of calcium phosphate (bone) and calcium carbonate (shell). Skulan and DePaolo (1999) showed that chickens have 2% δ44/42Ca between a hen's bones and an egg white; this span represents more than 80% of the entire range of natural Ca isotope variation and illustrates there is significant variation to investigate. A striking feature of archosaurian development that also occurs in many mammals, including humans, is mass transfer of calcium from mother to embryo. The yolk of the domestic hen matures over 7-9 days, but the albumen, shell membranes and shell form in less than 20 hours. Domestic laying hens are at the physiological limit of egg production and selective breeding is no longer an effective method of increasing egg production. 60-75% of the shell's ~1.5 g of calcium comes from dietary sources, while 25-40% comes from the hen's medullary bone. Medullary bone is spicules formed in the marrow of long bones, and is a store of dietary calcium rapidly available for eggshell secretion. During in ovo development, the embryo's skeleton is formed from calcium in the yolk and by bulk dissolution of the eggshell's inner aspect via carbonic anhydrase in a process that has an effect on bone density similar to

  2. Petrogenesis of Tertiary continental intra-plate lavas between Siebengebirge and Westerwald, Germany: Constraints from trace element systematics and Nd, Sr and Pb isotopes

    NASA Astrophysics Data System (ADS)

    Schubert, S.; Jung, S.; Pfänder, J. A.; Hauff, F.; Garbe-Schönberg, D.

    2015-10-01

    New 39Ar/40Ar ages and major- and trace-element and radiogenic isotope data are presented for basanites and alkali basalts from the transition area between the Westerwald and Siebengebirge volcanic fields (Germany) that belongs to the Central European Volcanic Province (CEVP). The 39Ar/40Ar ages indicate ages of c. 24 and c. 5 Ma which are fully compatible with previous K/Ar ages indicating that the evolution of this volcanic field belongs to the Westerwald area (28-22 Ma and 5 Ma) rather than to the Siebengebirge area (26-23 Ma). Based on the occurrence of > 30 isolated volcanic plugs with a simple igneous history, this volcanic field can be viewed as a monogenetic volcanic field. Compositions of some basanites are primitive, whereas others and the alkali basalts show decreasing Cr and Ni contents and CaO/Al2O3 ratios. However, increasing TiO2, Al2O3 and incompatible elements (Sr, Zr, Y, Hf, Ta) concentrations with decreasing MgO indicating fractionation of mainly olivine with minor amounts of clinopyroxene and spinel can be noticed. Rare earth element systematics suggest that most of the alkaline rocks are generated by different degrees of melting (5%-10%) of a garnet-bearing peridotite containing some residual amphibole. Negative anomalies of Rb and K in primitive mantle-normalized diagrams and a lack of Ba/Rb fractionation suggest that amphibole was the major OH-bearing mineral phase in the mantle. The alkaline rocks have a restricted range in 87Sr/86Sr and 143Nd/144Nd ratios ranging from 0.7033 to 0.7044 and from 0.51275 to 0.51285, respectively. Lead isotope compositions (206Pb/204Pb: 19.21-19.65; 207Pb/204Pb: 15.62-15.67; 208Pb/204Pb: 39.10-39.46) of the alkaline rocks are within the range of most OIB in which the higher values approach the composition of the European Asthenospheric Reservoir (EAR). The correlation between Sr and Nd isotopes and trace element constraints (Ce/Pb; Nb/U) indicates that for some samples interaction with crustal rocks during

  3. Importance of the Lu-Hf isotopic system in studies of planetary chronology and chemical evolution

    USGS Publications Warehouse

    Patchett, P.J.

    1983-01-01

    The 176Lu-176Hf isotope method and its applications in earth sciences are discussed. Greater fractionation of Lu/Hf than Sm/Nd in planetary magmatic processes makes 176Hf 177Hf a powerful geochemical tracer. In general, proportional variations of 176Hf 177Hf exceed those of 143Nd l44Nd by factors of 1.5-3 in terrestrial and lunar materials. Lu-Hf studies therefore have a major contribution to make in understanding of terrestrial and other planetary evolution through time, and this is the principal importance of Lu-Hf. New data on basalts from oceanic islands show unequivocally that whereas considerable divergences occur in 176Hf 177Hf- 87Sr 86Sr and 143Nd l44Nd- 87Sr 86Sr diagrams, 176Hf 177Hf and 143Nd 144Nd display a single, linear isotopic variation in the suboceanic mantle. These discordant 87Sr 86Sr relationships may allow, with the acquisition of further Hf-Nd-Sr isotopic data, a distinction between processes such as mantle metasomatism, influence of seawater-altered material in the magma source, or recycling of sediments into the mantle. In order to evaluate the Hf-Nd isotopic correlation in terms of mantle fractionation history, there is a need for measurements of Hf distribution coefficients between silicate minerals and liquids, and specifically for a knowledge of Hf behavior in relation to rareearth elements. For studying ancient terrestrial Hf isotopic variations, the best quality Hf isotope data are obtained from granitoid rocks or zircons. New data show that very U-Pb discordant zircons may have upwardly-biased 176Hf 177Hf, but that at least concordant to slightly discordant zircons appear to be reliable carriers of initial 176Hf 177Hf. Until the controls on addition of radiogenic Hf to zircon are understood, combined zircon-whole rock studies are recommended. Lu-Hf has been demonstrated as a viable tool for dating of ancient terrestrial and extraterrestrial samples, but because it offers little advantage over existing methods, is unlikely to find

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

    USGS Publications Warehouse

    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.

  5. Interrogating pollution sources in a mangrove food web using multiple stable isotopes.

    PubMed

    Souza, Iara da C; Arrivabene, Hiulana P; Craig, Carol-Ann; Midwood, Andrew J; Thornton, Barry; Matsumoto, Silvia T; Elliott, Michael; Wunderlin, Daniel A; Monferrán, Magdalena V; Fernandes, Marisa N

    2018-06-01

    Anthropogenic activities including metal contamination create well-known problems in coastal mangrove ecosystems but understanding and linking specific pollution sources to distinct trophic levels within these environments is challenging. This study evaluated anthropogenic impacts on two contrasting mangrove food webs, by using stable isotopes (δ 13 C, δ 15 N, 87 Sr/ 86 Sr, 206 Pb/ 207 Pb and 208 Pb/ 207 Pb) measured in sediments, mangrove trees (Rhizophora mangle, Laguncularia racemosa, Avicennia schaueriana), plankton, shrimps (Macrobranchium sp.), crabs (Aratus sp.), oysters (Crassostrea rhizophorae) and fish (Centropomus parallelus) from both areas. Strontium and Pb isotopes were also analysed in water and atmospheric particulate matter (PM). δ 15 N indicated that crab, shrimp and oyster are at intermediate levels within the local food web and fish, in this case C. parallelus, was confirmed at the highest trophic level. δ 15 N also indicates different anthropogenic pressures between both estuaries; Vitória Bay, close to intensive human activities, showed higher δ 15 N across the food web, apparently influenced by sewage. The ratio 87 Sr/ 86 Sr showed the primary influence of marine water throughout the entire food web. Pb isotope ratios suggest that PM is primarily influenced by metallurgical activities, with some secondary influence on mangrove plants and crabs sampled in the area adjacent to the smelting works. To our knowledge, this is the first demonstration of the effect of anthropogenic pollution (probable sewage pollution) on the isotopic fingerprint of estuarine-mangrove systems located close to a city compared to less impacted estuarine mangroves. The influence of industrial metallurgical activity detected using Pb isotopic analysis of PM and mangrove plants close to such an impacted area is also notable and illustrates the value of isotopic analysis in tracing the impact and species affected by atmospheric pollution. Copyright © 2018 Elsevier B

  6. OIB signatures in basin-related lithosphere-derived alkaline basalts from the Batain basin (Oman) - Constraints from 40Ar/39Ar ages and Nd-Sr-Pb-Hf isotopes

    NASA Astrophysics Data System (ADS)

    Witte, M.; Jung, S.; Pfänder, J. A.; Romer, R. L.; Mayer, B.; Garbe-Schönberg, D.

    2017-08-01

    Tertiary rift-related intraplate basanites from the Batain basin of northeastern Oman have low SiO2 (< 45.6 wt.%), high MgO (> 9.73 wt.%) and moderate to high Cr and Ni contents (Cr > 261 ppm, Ni > 181 ppm), representing near primary magmas that have undergone fractionation of mainly olivine and magnetite. Rare earth element systematics and p-T estimates suggest that the alkaline rocks are generated by different degrees of partial melting (4-13%) of a spinel-peridotite lithospheric mantle containing residual amphibole. The alkaline rocks show restricted variations of 87Sr/86Sr and 143Nd/144Nd ranging from 0.70340 to 0.70405 and 0.51275 to 0.51284, respectively. Variations in Pb isotopes (206Pb/204Pb: 18.59-18.82, 207Pb/204Pb: 15.54-15.56, 208Pb/204Pb: 38.65-38.98) of the alkaline rocks fall in the range of most OIB. Trace element constraints together with Sr-Nd-Pb isotope composition indicate that assimilation through crustal material did not affect the lavas. Instead, trace element variations can be explained by melting of a lithospheric mantle source that was metasomatized by an OIB-type magma that was accumulated at the base of the lithosphere sometimes in the past. Although only an area of less than 1000 km2 was sampled, magmatic activity lasted for about 5.5 Ma with a virtually continuous activity from 40.7 ± 0.7 to 35.3 ± 0.6 Ma. During this period magma composition was nearly constant, i.e. the degree of melting and the nature of the tapped source did not change significantly over time.

  7. Accurate isotopic fission yields of electromagnetically induced fission of 238U measured in inverse kinematics at relativistic energies

    NASA Astrophysics Data System (ADS)

    Pellereau, E.; Taïeb, J.; Chatillon, A.; Alvarez-Pol, H.; Audouin, L.; Ayyad, Y.; Bélier, G.; Benlliure, J.; Boutoux, G.; Caamaño, M.; Casarejos, E.; Cortina-Gil, D.; Ebran, A.; Farget, F.; Fernández-Domínguez, B.; Gorbinet, T.; Grente, L.; Heinz, A.; Johansson, H.; Jurado, B.; Kelić-Heil, A.; Kurz, N.; Laurent, B.; Martin, J.-F.; Nociforo, C.; Paradela, C.; Pietri, S.; Rodríguez-Sánchez, J. L.; Schmidt, K.-H.; Simon, H.; Tassan-Got, L.; Vargas, J.; Voss, B.; Weick, H.

    2017-05-01

    SOFIA (Studies On Fission with Aladin) is a novel experimental program, dedicated to accurate measurements of fission-fragment isotopic yields. The setup allows us to fully identify, in nuclear charge and mass, both fission fragments in coincidence for the whole fission-fragment range. It was installed at the GSI facility (Darmstadt), to benefit from the relativistic heavy-ion beams available there, and thus to use inverse kinematics. This paper reports on fission yields obtained in electromagnetically induced fission of 238U.

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  9. 87Sr/86Sr and 143Nd/144Nd for disentangling anthropogenic and natural REE contributions in river water during flood events.

    NASA Astrophysics Data System (ADS)

    Hissler, Christophe; Stille, Peter; Pfister, Laurent

    2017-04-01

    The sustainable management of water resources is one of the greatest challenges of the 21st century. Water is a vital resource that is increasingly put under pressure from multiple perspectives. While the global population is on the rise, socio-economic development makes equally rapid progress - eventually compromising access to clean water bodies. Multiple pollution sources constitute an immediate threat to aquatic ecosystems and are likely to cause long lasting contaminations of water bodies that are critical for drinking and/or irrigation water production. There is a pressing need for an adequate quantification of anthropogenic impacts on the critical zone of river basins and the identification of the temporal dynamics of these impacts. As an example, despite the work done to assess the environmental impact of REE pollutions in larger river systems, we are still lacking information on the dynamics of these anthropogenic compounds in relation to rapid hydrological changes. Filling these knowledge gaps is a pre-requisite for the design and implementation of sustainable water resources management strategies. In order to better constrain the relative contributions of both anthropogenic and geogenic trace element sources we propose using a multitracer approach combining elemental and 87Sr/86Sr, 143Nd/144Nd, and 206Pb/207Pb isotopic ratios. The use of these three separate isotopic systems together with REE concentrations is new in the field of anthropogenic source identification in river systems. We observed enrichments in Anthropogenic Rare Earth Elements (AREE) for dissolved Gd and suspended Nd loads of river water. With increasing discharge, AREE anomalies progressively disappeared and gave way to the geogenic chemical signature of the basin in both dissolved and suspended loads. The isotopic data confirm these observations and shed new light on the trace elements sources. On the one hand, dissolved loads have peculiar isotopic characteristics and carry mainly

  10. Tracing Altiplano-Puna plateau surface uplift via radiogenic isotope composition of Andean arc lavas

    NASA Astrophysics Data System (ADS)

    Scott, E. M.; Allen, M. B.; Macpherson, C.; McCaffrey, K. J. W.; Davidson, J.; Saville, C.

    2016-12-01

    We have compiled published geochemical data for Jurassic to Holocene Andean arc lavas from 5oN to 47oS, covering the current extent of the northern, central and southern volcanic zones. Using this dataset we evaluate the spatial and temporal evolution of age corrected Sr- and Nd-radiogenic isotopes in arc lavas at a continental-scale, in order to understand the tectonic and surface uplift histories of the Andean margin. It has long been noted that baseline 87Sr/86Sr and 143Nd/144Nd ratios of Quaternary lavas from the central volcanic zone, located within the Altiplano-Puna plateau, are distinct from volcanic rocks to the north and south. This is commonly attributed to greater crustal thickness, which increases to roughly twice that of the average continental crust within the Altiplano-Puna plateau. By comparing 87Sr/86Sr and 143Nd/144Nd ratios in Quaternary lavas to published crustal thickness models, present day topography and the compositions of basement terranes, we note that Sr- and Nd-isotope values of Quaternary lavas are an effective proxy for present day regional elevation. In contrast, variation in basement terranes has only a small, second order effect on isotopic composition at the scale of our study. Using this isotopic proxy, we infer the spatial extent of the plateau and its surface uplift history from the Jurassic to the present. Our results concur with a crustal thickening model of continued surface uplift, which initiated in the Altiplano, with deformation propagating southwards into the Puna throughout the Neogene and then continuing in central Chile and Argentina up to the present day.

  11. Constraining the mechanisms driving coccolith δ44/40Ca and Sr/Ca variations: new perspectives from cultures, cellular models, and the sediment record

    NASA Astrophysics Data System (ADS)

    María Mejía, Luz; Paytan, Adina; Eisenhauer, Anton; Kolevica, Ana; Bolton, Clara; Méndez-Vicente, Ana; Abrevaya, Lorena; Isensee, Kirsten; Stoll, Heather

    2017-04-01

    Coccoliths comprise a major fraction of the calcium carbonate (CaCO3) production, with contributions varying from 95% of the global carbonate sink during the Cenozoic, to 50% in the modern ocean. Therefore, significant changes in coccolith Ca isotopic fractionation could have affected past seawater Ca isotopic composition (δ44/40Ca), with potential important implications for the interpretation of the global Ca cycle and related changes in seawater chemistry. Here we evaluate the mechanisms driving coccolith Ca isotopic fractionation in a quantitative framework, by deriving a steady-state mass balance geochemical model (CaSri-Co), which assumes that fractionation is solely associated with desolvation (i.e. dehydration) of Ca during cellular transport through membranes. The application of the CaSri-Co model to previously published and to our new δ44/40Ca and Sr/Ca results from cultured coccolithophores (Emiliania huxleyi, Gephyrocapsa oceanica and Calcidiscus leptoporus) allowed us to identify calcification rates, Ca retention efficiency and water structure strength as main regulators of the Ca isotopic fractionation and Sr/Ca ratios of cultured coccolith calcite. Higher calcification rates, higher Ca retention efficiencies and higher water structure strength (slower Ca solvation-desolvation reactions) increase both coccolith Sr/Ca and Ca isotopic fractionation. The CaSri-Co model shows that coccolith Ca isotopic fractionation is especially sensitive to changes in water structure strength. On the other hand, Ca retention efficiency appears to be the main driver of the observed Sr/Ca trends, which results from the incomplete usage of the Sr transported to the calcification vesicle and subsequent Sr enrichment of the cytosol, while Ca inside the calcification vesicle is assumed to be completely utilized in the model. In this study we also measured δ44/40Ca and Sr/Ca in two coccolith size fraction from site 925 in the Western Equatorial Atlantic representing the last

  12. Nucleosynthetic Heterogeneity Controls Vanadium Isotope Variations in Bulk Chondrites

    NASA Technical Reports Server (NTRS)

    Nielsen, S. G.; Righter, K.; Wu, F.; Owens, J. D.; Prytulak, J.; Burton, K.; Parkinson, I.; Davis, D.

    2018-01-01

    The vanadium (V) isotope composition of early solar system materials have been hypothesized to be sensitive to high energy irradiation that originated from the young Sun. Vanadium has two isotopes with masses 50 and 51 that have (51)V/(50)V ratio of approximately 410. High energy irradiation produces (50)V from various target isotopes of Ti, Cr and Fe, which would result in light V isotope compositions (expressed as delta (51)V in per mille = 1000 x (((51)V/(50)V(sub sample)/(51)V/(50)V(sub AlfaAesar)) - 1)) relative to a presumably chondritic starting composition. Recently published V isotope data for calcium aluminium inclusions (CAIs) has revealed some very negative values relative to chondrites (by almost -4 per mille) that were indeed interpreted to reflect irradiation processes despite the fact that the studied CAIs all exhibited significant initial abundances of (10)Be, while only a few CAIs displayed light V isotope compositions. It is difficult to relate V isotope variations directly to a singular process because V only possesses two isotopes. Therefore, V isotope variations can principally be produced both mass dependent and independent processes. Mass dependent kinetic stable isotope fractionation is common in CAIs for refractory elements due to partial condensation/evaporation processes. The element strontium (Sr) has an almost identical condensation temperature to V and studies of stable Sr isotope compositions in CAIs reveal both heavy and light values relative to chondrites of several permil. These variations are similar in magnitude to those reported for V isotopes in CAIs, which suggests it is possible that some of the V isotope variation in CAIs could be due to kinetic stable isotope fractionation during condensation/evaporation processes.

  13. Constraints on Ca/Sr as a Proxy for Calcium in Forest Ecosystems

    NASA Astrophysics Data System (ADS)

    Hoff, C. J.; Hobbie, E. A.; Hallett, R.; Colpaert, J.; Bryce, J. G.

    2004-05-01

    Calcium is a key plant nutrient and important base cation in ecosystems. Our current efforts to quantify Ca cycling in ecosystems rely on indirect proxies, e.g., Ca/Sr or Sr isotopic systems (1). An important assumption in these applications is that the elemental ratio of calcium to strontium faithfully represents calcium cycling and that little fractionation occurs through biogeochemical and physiological processes. However, several researchers have reported variations in Ca/Sr, e.g. among different tree tissues (2) and during weathering processes (3), raising doubts about the suitability of the proxy. To address the question of reliability, we measured Ca/Sr values in a culture study in which Scots pines were grown at low or high nutrient supply rates (3% per day or 5% per day). Because mycorrhizal fungi are intimately involved in plant nutrient supply, plants were also grown either uncolonized or colonized with one of two different species of mycorrhizal fungi (Suillus luteus and Thelephora terrestris). Our preliminary results indicate that Ca/Sr values differ between high and low nutrient treatments, root and foliage, and mycorrhizal treatments. In individual seedlings, roots have lower Ca/Sr than foliage by absolute factors of 2-5. The magnitude of the effect is apparently determined by a combination of environmental factors including both the nutrient and mycorrhizal treatments. These results indicate that Ca and Sr are partitioned differently between nutrient and mycorrhizal treatments and between plant fractions despite the common nutrient broth and substrate. Thus, Ca/Sr values alone are not reliable tracers of Ca within an ecosystem because of partitioning of Ca and Sr during nutrient transport within the plant-mycorrhizal system. We are presently refining analytical techniques and conducting leachate experiments to improve the quantification of this Ca/Sr fractionation. We are also exploring the use of isotopic tracers to study calcium biogeochemical

  14. Anatexis of mafic and felsic lower crust: Geochemistry and Nd, Sr and Pb isotopes of late-orogenic granodiorites and leucogranites (Damara orogen, Namibia)

    NASA Astrophysics Data System (ADS)

    Osterhus, Lennart; Jung, Stefan

    2010-05-01

    The Damara orogen (Namibia) represents a well-exposed and deeply eroded orogenic mobile belt consisting of the north-south trending Kaoko belt and the northeast-southwest trending intracontinental Damara belt. The latter has been subdivided into a Northern, a Central and a Southern Zone based on stratigraphy, metamorphic grade, structure and geochronology. The late-orogenic granodioritic to leucogranitic Gawib pluton is a cross-cutting, pear-shaped post-tectonic stock within the southern Central Zone which is elsewhere dominated by basement rocks, high-grade metasedimentary rocks of the Tinkas Formation and syn-orogenic granites (Salem-type). The non-foliated granodiorites consist of plagioclase, quartz, microcline, hornblende and biotite whereas the leucogranites consist of microcline, quartz, plagioclase and biotite. Major element variation of the granodiorites show two distinct magma types were some samples have high TiO2, MgO and Fe2O3 and low Al2O3 and others have low TiO2, MgO and Fe2O3 and high Al2O3. Based on high REE, Nb, Zr and Y concentrations some granodiorites can be classified as A-type granitoids. Strontium concentrations are high in the granodiorites (up to 939 ppm) and decrease to < 200 ppm in the leucogranites. Rb/Sr ratios are low (1) in the leucogranites. Granodiorites have moderately radiogenic initial 87Sr/86Sr ratios (0.7088-0.7132), strongly negative initial ɛ Nd values (ca. -12) and comparatively unradiogenic Pb isotope data, the latter obtained on acid-leached feldspar separates. Leucogranites have more radiogenic initial 87Sr/86Sr ratios (0.7223-0.7336) and more negative initial ɛ Nd values (ca. -18). Pb isotopes tend to be less radiogenic than in the granodiorites. The mean crustal residence ages of the granodiorites, expressed as depleted mantle Nd model ages, are ca. 2.0 Ga but the leucogranites tend to have older Nd model ages (2.5 Ga). Therefore, a likely source for the granodiorites and leucogranites is a sequence of mafic to

  15. Sm-Nd and Rb-Sr Isotopic Studies of Meteorite Kalahari 009: An Old VLT Mare Basalt

    NASA Technical Reports Server (NTRS)

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

    2008-01-01

    Lunar meteorite Kalahari 009 is a fragmental basaltic breccia contain ing various very-low-Ti (VLT) mare basalt clasts embedded in a fine-g rained matrix of similar composition. This meteorite and lunar meteorite Kalahari 008, an anorthositic breccia, were suggested to be paired mainly due to the presence of similar fayalitic olivines in fragment s found in both meteorites. Thus, Kalahari 009 probably represents a VLT basalt that came from a locality near a mare-highland boundary r egion of the Moon, as compared to the typical VLT mare basalt samples collected at Mare Crisium during the Luna-24 mission. The concordant Sm-Nd and Ar-Ar ages of such a VLT basalt (24170) suggest that the extrusion of VLT basalts at Mare Crisium occurred 3.30 +/- 0.05 Ga ag o. Previous age results for Kalahari 009 range from approximately 4.2 Ga by its Lu-Hf isochron age to 1.70?0.04 Ga of its Ar-Ar plateau ag e. However, recent in-situ U-Pb dating of phosphates in Kalahari 009 defined an old crystallization age of 4.35+/- 0.15 Ga. The authors su ggested that Kalahari 009 represents a cryptomaria basalt. In this r eport, we present Sm-Nd and Rb-Sr isotopic results for Kalahari 009, discuss the relationship of its age and isotopic characteristics to t hose of other L-24 VLT mare basalts and other probable cryptomaria ba salts represented by Apollo 14 aluminous mare basalts, and discuss it s petrogenesis.

  16. Isotope shift of the 590-cm-1 Raman feature in underdoped Bi2Sr2CaCu2O8+δ

    NASA Astrophysics Data System (ADS)

    Hewitt, K. C.; Wang, N. L.; Irwin, J. C.; Pooke, D. M.; Pantoja, A. E.; Trodahl, H. J.

    1999-10-01

    Raman-scattering studies have been performed on underdoped Bi2Sr2CaCu2O8+δ. In single crystals underdoped by oxygen removal, a 590-cm-1 peak is observed in the B1g spectrum. The feature is observed to soften in frequency by 3.8% with isotopic exchange of 16O by 18O. In contrast, the 590-cm-1 peak is not observed in crystals underdoped by Y substitution which suggests that it is a vibrational mode activated by oxygen deficency. We have also found that underdoping leads to a depletion of low-energy spectral weight from regions of the Fermi surface located near the Brillouin-zone axes.

  17. 40Ar/39Ar geochronology, elemental and Sr-Nd-Pb isotope geochemistry of the Neogene bimodal volcanism in the Yükselen area, NW Konya (Central Anatolia, Turkey)

    NASA Astrophysics Data System (ADS)

    Gençoğlu Korkmaz, Gülin; Asan, Kürşad; Kurt, Hüseyin; Morgan, Ganerød

    2017-05-01

    Bimodal volcanic suites occur in both orogenic and anorogenic geotectonic settings. Although their formation can be attributed to either fractional crystallization from basaltic parents to felsic derivatives or partial melting of different sources, the origin of bimodal suites is still unclear. By reporting mineral chemistry, 40Ar/39Ar geochronology, elemental and Sr-Nd-Pb isotope geochemistry data, this study aims to investigate the genesis of bimodal basalt-dacite association from the Yükselen area located on the northern end of the Sulutas Volcanic Complex (Konya, Central Anatolia). The Yükselen area volcanic rocks are represented by basaltic lava flows, and dacitic dome with enclaves and pyroclastics. Basaltic flows and pyroclastic rocks are interlayered with the Neogene fluvio-lacustrine sedimentary units, while dacitic rocks cut the pre-Neogene basement in the area. A biotite separation from dacites yielded 40Ar/39Ar plateau age of 16.11 ± 0.18 Ma. On the other hand, a whole rock sample from basalts gave two plateau ages of 16.45 ± 0.76 Ma and 22.37 ± 0.65 Ma for the first steps and next steps, respectively. The investigated basalts are sodic alkaline, and characterized by ocean island basalt (OIB)-like anorogenic geochemical signatures. However, dacites are calc-alkaline and metaluminous, and carry geochemical signatures of orogenic adakites. Sr-Nd-Pb isotopic systematics suggest that the basalts were derived from an asthenospheric mantle source enriched by recycled crustal rocks. The dacites show more enriched Sr and Pb ratios and more depleted Nd ones relative to the basalts, which at the first glance might be attributed to crustal contamination of the associated basalts. However, trace element features of the dacites rule out cogenetic relationship between the two rock types, and point to an origin by melting of lower crust. On the other hand, enclaves share several elemental and isotopic characteristics with the dacites, and appear to be fragments

  18. Dating the Indo-Asia collision in NW Himalaya: constraints from Sr-Nd isotopes and detrital zircon (U-Pb) and Hf isotopes of Paleogene-Neogene rocks in the Katawaz basin, NW Pakistan

    NASA Astrophysics Data System (ADS)

    Zhuang, Guangsheng; Najman, Yani; Millar, Ian; Chauvel, Catherine; Guillot, Stephane; Carter, Andrew

    2015-04-01

    The time of collision between the Indian and Asian plates is key for understanding the convergence history and the impact on climatic systems and marine geochemistry. Despite much active research, the fundamental questions still remain elusive regarding when and where the Indian plate collided with the Asian plate. Especially in the west Himalaya, the questions become more complex due to disputes on the amalgamation history of interoceanic Kohistan-Ladakh arcs (KLA) with Karakoram of the Asian plate and the Indian plate. Here, we present a result of multiple-isotopic geochemistry and geochronology study in the Katawaz Basin in NW Pakistan, a remnant oceanic basin on the western Indian plate which was the repository for the sediments eroded from the west Himalaya ( Qayyum et al., 1996, 1997a, 1997b, 2001; Carter et al., 2010), to evaluate the time and character of collision in this region. In this study, we analyzed 22 bulk mudstone samples for Sr-Nd isotopes and 11 medium-grained sandstones for detrital zircon (U-Pb) geochronology and Hf isotopes. We constructed the Cenozoic chronology in the Katawaz Basin based on our newly collected detrital zircon U-Pb ages and fission track ages. We present the first record of Katawaz chronology that constrained the Khojak Formation to be < 40 Ma to < 22 Ma. The result is consistent with the previous nanofossil study that constrained the upper part of underlying Nisai Formation to be the Middle to Late Eocene. Our current study revealed that the Katawaz sedimentary sequence ranges in age from Eocene to the earliest Miocene. The samples from the Nisai Formation show the 87Sr/86Sr - ɛNd values overlapping those of the end member of the Karakoram of Asian origin, revealing the arrival of Asian detritus on the Indian plate prior to 50 Ma. There are two parallel lines of evidence supporting this conclusion: (1) young zircon grains (< 120 Ma), characterizing the KLA and Karakoram, persistently exist throughout the whole sedimentary

  19. Fluid inclusion, geochemical, Rb-Sr and Sm-Nd isotope studies on tungsten mineralized Degana and Balda granites of the Aravalli craton, NW India

    NASA Astrophysics Data System (ADS)

    Vijay Anand, Sundarrajan; Pandian, M. S.; Balakrishnan, S.; Sivasubramaniam, R.

    2018-06-01

    Granitic plutons occurring within and to the west of the Delhi Fold Belt in the Aravalli craton, northwestern India are the result of widespread felsic magmatism during Neoproterozoic, some of which are associated with greisen and skarn tungsten deposits. In this paper, we present the result of our study on fluid inclusions, geochemistry and geochronology of two such tungsten mineralized granite plutons at Degana and Balda, and interpret the nature of ore fluid, and petrogenesis and age of these mineralized granites. Fluid inclusion study reveals coexistence of moderate and hyper-saline aqueous fluid inclusions along with aqueous-carbonic inclusions, suggesting their origin due to liquid immiscibility during fluid-rock interaction. Geochemically, the granites are peraluminous, Rb enriched, Sr and Ba depleted and highly differentiated. The Rb-Sr isotopic systematics yielded 795± 11 Ma for Balda granite and 827± 8 Ma for Degana granite. We show that major phase of widespread granitoid magmatism and mineralization during the Neoproterozoic (840-790 Ma) in NW India is coeval with breakup of the Rodinia supercontinent and infer a causal relationship between them.

  20. O, Sr and Nd isotopic constraints on Cenozoic granitoids of Northwestern Anatolia, Turkey: Enrichment by subduction zone fluids

    NASA Astrophysics Data System (ADS)

    Yücel-Öztürk, Yeşim

    2016-05-01

    The oxygen and strontium isotope compositions of Cenozoic granitoids cropping out in the İzmir-Ankara-Erzincan suture zone help constrain the petrological evolution of magmatism in northwest Anatolia. The magmatism was mostly widespread between late Eocene (∼37 Ma) and the middle Miocene (∼14-15 Ma), and is represented by volcanic and plutonic rocks of orogenic affinity, of which Ezine, Eğrigöz, Çataldağ and Kozak are the largest Tertiary granitic plutons exposed in northwest Anatolia. They vary from granite to granodiorite, and are subalkaline, belonging to the high-K calc-alkaline I-type granite series. All these characteristics, combined with major, trace element geochemical data as well as mineralogical and textural evidence, reveal that the Oligocene-Miocene granitoids of NW Anatolia are comparable with volcanic arc granites, formed in a transitional oceanic to continental collisional tectonic setting, from a hybrid source, having crustal and mantle components that underwent further interaction with the upper crust. These plutons have initial 87Sr/86Sr ratios of 0.7072-0.7094, and εNd(t) values ranging from -3.48 to -1.20. These characteristics also indicate that a crustal component played an important role in the petrogenesis of NW Anatolian Oligocene-Miocene granitoids. The moderately evolved Ezine, Eğrigöz, Çataldağ and Kozak granitoids, have δ18O values that are consistent with those of normal I-type granites (6-10‰), but the δ18O relationships among minerals of samples collected from the intrusive contacts which are closest to mineralized zones, indicate a major influence of hydrothermal processes under subsolidus conditions. The oxygen isotope systematics of the samples from these plutons result from the activity of high-δ18O fluids (magmatic water), with major involvement of low-δ18O fluids (meteoric water) evident, near the edge zone of these plutons. This is most evident in δ18O quartz-feldspar pairs from these granitoids, which

  1. Isotopic evidence for closed-system anatexis at midcrustal levels: An example from the Acadian Appalachians of New England

    NASA Astrophysics Data System (ADS)

    Lathrop, Alison S.; Blum, Joel D.; Chamberlain, C. Page

    1994-05-01

    We have investigated the Sr and O isotope systematics of granitoid and metasedimentary samples from the Central Main Terrane (CMT) of New England. Granitoid samples were taken from interior and contact zones within the Acadian-aged (approximately 410 m.y.), synmetamorphic and syntectonic Kinsman Quartz Monzonite (KQM), which is a member of the New Hampshire Plutonic Series. Metasedimentary samples were taken from Silurian and Devonian formations hosting the KQM. Initial Sr isotope ratios (Sr(sub i) and delta O-18 values for the KQM range from 0.70799 to 0.71246 and 7.6% to 12.9%, respectively, and Sr(sub i) and delta O-18 values of the metasedimentary rocks range from 0.70770 to 0.75008 and 6.2% to 14.1%, respectively. We observe a linear and slightly positive correlation between Sr(sub i) and delta O-18 for interior KQM samples that can be duplicated by a mixing curve calculated for metasedimentary endmembers, whereas the Sr(sub i) and delta O-18 values of contact KQM samples cluster near the Sr(sub i) and delta O-18 values of the metasedimentary rocks with which they are in contact. Mixing calculations provide no evidence for a measurable primitive mantle component in either interior or contact KQM samples, and we conclude that the Sr-O isotopic composition of the KQM is most likely a reflection of isotopic heterogeneities inherited from a complex package of midcrustal metasedimentary source rocks. We propose that the KQM is the product of midcrustal partial melting that was initiated due to excess thermal energy from the decay of anomalously high concentrations of heat-producing elements in Silurian source rocks within the CMT. Because we see no isotopic evidence for a lower-crustal or mantle component in the KQM, we suggest that midcrustal anatexis may have occurred as a closed-system process, requiring no accompanying mantle-derived magma or above normal mantle heat flow.

  2. Integrated Sr isotope variations and global environmental changes through the Late Permian to early Late Triassic

    NASA Astrophysics Data System (ADS)

    Song, Haijun; Wignall, Paul B.; Tong, Jinnan; Song, Huyue; Chen, Jing; Chu, Daoliang; Tian, Li; Luo, Mao; Zong, Keqing; Chen, Yanlong; Lai, Xulong; Zhang, Kexin; Wang, Hongmei

    2015-08-01

    New 87Sr/86Sr data based on 127 well-preserved and well-dated conodont samples from South China were measured using a new technique (LA-MC-ICPMS) based on single conodont albid crown analysis. These reveal a spectacular climb in seawater 87Sr/86Sr ratios during the Early Triassic that was the most rapid of the Phanerozoic. The rapid increase began in Bed 25 of the Meishan section (GSSP of the Permian-Triassic boundary, PTB), and coincided closely with the latest Permian extinction. Modeling results indicate that the accelerated rise of 87Sr/86Sr ratios can be ascribed to a rapid increase (>2.8×) of riverine flux of Sr caused by intensified weathering. This phenomenon could in turn be related to an intensification of warming-driven runoff and vegetation die-off. Continued rise of 87Sr/86Sr ratios in the Early Triassic indicates that continental weathering rates were enhanced >1.9 times compared to those of the Late Permian. Continental weathering rates began to decline in the middle-late Spathian, which may have played a role in the decrease of oceanic anoxia and recovery of marine benthos. The 87Sr/86Sr values decline gradually into the Middle Triassic to an equilibrium values around 1.2 times those of the Late Permian level, suggesting that vegetation coverage did not attain pre-extinction levels thereby allowing higher runoff.

  3. Origin of enormous trace metal enrichments in weathering mantles of Jurassic carbonates: evidence from Sr, Nd and Pb isotopes

    NASA Astrophysics Data System (ADS)

    Hissler, C.; Stille, P.; Juilleret, J.; Iffly, J.; Perrone, T.; Morvan, G.

    2013-12-01

    Weathering mantels are widespread worldwide and include lateritic, sandy and kaolinite-rich saprolites and residuals of partially dissolved carbonate rocks. These old regolith systems have a complex history of formation and may present a polycyclic evolution due to successive geological and pedogenetic processes that affected the profile. Until now, only few studies highlighted the unusual content of associated trace elements in this type of weathering mantle. For instance, these enrichments can represent about five times the content of the underlying Bajocian to Oxfordian limestone/marl complexes, which have been relatively poorly studied compared to weathering mantle developed on magmatic bedrocks. Up to now, neither soil, nor saprolite formation has to our knowledge been geochemically elucidated. Therefore, the aim of this study was to examine more closely the soil forming dynamics and the relationship of the chemical soil composition to potential sources (saprolite, Bajocian silty marls and limestones, atmospheric particles deposition...). Of special interest has also been the origin of trace metals and the processes causing their enrichments. Especially Rare Earth Element (REE) distribution patterns and Sr, Nd and Pb isotope ratios are particularly well suited to identify trace element migration, to recognize origin and mixing processes and, in addition, to decipher possible anthropogenic and/or "natural" atmosphere-derived contributions to the soil. Moreover, leaching experiments shall help to identify mobile phases in the soil system. This may inform on the stability of trace elements and especially on their behaviour in these Fe-enriched carbonate systems. Trace metal migration and enrichments were studied on a cambisol developing on an underlying Jurassic limestone. The base is strongly enriched among others in rare earth elements (ΣREE: 2640ppm) or redox-sensitive elements such as Fe (44 wt.%), V (920ppm), Cr (700ppm), Zn (550ppm), As (260ppm), Co (45ppm

  4. Land use and mobility during the Neolithic in Wales explored using isotope analysis of tooth enamel

    PubMed Central

    Montgomery, Janet; Evans, Jane; Cook, Gordon T.; Scarre, Chris

    2017-01-01

    Abstract Objectives The nature of land use and mobility during the transition to agriculture has often been debated. Here, we use isotope analysis of tooth enamel from human populations buried in two different Neolithic burial monuments, Penywyrlod and Ty Isaf, in south‐east Wales, to examine patterns of land use and to evaluate where individuals obtained their childhood diet. Materials and Methods We employ strontium (87Sr/86Sr) and oxygen (δ18O) and carbon (δ13C) isotope analysis of enamel from adjacent molars. We compare strontium isotope values measured in enamel to locally bioavailable 87Sr/86Sr values. We combine discussion of these results with evaluation of new radiocarbon dates obtained from both sites. Results The majority of enamel samples from Penywyrlod have strontium isotope ratios above 0.7140. In contrast, the majority of those from Ty Isaf have 87Sr/86Sr values below 0.7140. At Penywyrlod oxygen isotope ratios range between 25.9 and 28.2 ‰ (mean 26.7 ± 0.6 ‰, 1σ, n = 15) and enamel δ13Ccarbonate values range between −18.0 and −15.0 ‰ (mean −16.0 ± 0.8 ‰, 1σ, n = 15). At Ty Isaf oxygen isotope ratios exhibited by Neolithic individuals range between 25.4 and 27.7 ‰ (mean 26.7 ± 0.6 ‰, 1σ, n = 15) and enamel δ13Ccarbonate values range between −16.9 and −14.9 ‰ (mean −16.0 ± 0.6 ‰, 1σ, n = 15). Discussion The strontium isotope results suggest that the majority of individuals buried at Penywyrlod did not source their childhood diet locally. One individual in this group has strontium isotope ratios that exceed all current known biosphere values within England and Wales. This individual is radiocarbon dated to the first few centuries of the 4th millennium BC, consistent with the period in which agriculture was initiated in Wales: the results therefore provide evidence for migration during the transition to farming in Wales. In contrast, all individuals sampled from Ty Isaf post

  5. Elemental and Sr-Nd isotopic geochemistry of the Uradzhongqi magmatic complex in western Inner Mongolia, China: A record of early Permian post-collisional magmatism

    NASA Astrophysics Data System (ADS)

    Qiao, Xueyuan; Li, Wenbo; Zhong, Richen; Hu, Chuansheng; Zhu, Feng; Li, Zhihua

    2017-08-01

    The magmatic complex in Uradzhongqi, Inner Mongolia, is located in the western segment of the northern margin of the North China Craton (NCC). The dominant components in the complex include syenogranite, monzogranite, granodiorite, diorite and gabbro. Mafic microgranular enclaves (MMEs) are common in syenogranite and granodiorite. Zircon U-Pb dating shows that the ages of these rocks range from 283 to 270 Ma, suggesting an early Permian emplacement. The syenogranite and monzogranite are peraluminous I-type granites, exhibiting conspicuous negative Eu anomaly, enrichment in large-ion lithophile elements (LILE) and light rare earth elements (LREE), depletion in high field strength elements (HFSE). The granodiorites, diorites and MMEs are metaluminous in composition, show high Al2O3, MgO and Fe2O3T contents and weak negative Eu anomaly, as well as LREE and LILE enrichment and HFSE depletion. The gabbros show weak positive Eu anomaly and slight REE differentiation. The Sr-Nd isotope compositions show that the source of mafic magma was depleted mantle (DM) with possible involvement of enriched mantle II (EM II), whereas the felsic magma was derived from the Archean lower crust. Petrographic observation and analytical results of mineralogy, geochronology, geochemistry and Sr-Nd isotopes indicate that the main petrogenesis of these magmatic rocks is the mixing of underplating mafic magma and felsic magma. Tectonically, the complex pluton was formed within a post-collisional regime, and the underplating in this area provides another piece of evidence for the vertical growth of the western segment of the northern margin of the NCC.

  6. Rb, Sr, Nd, and Sm concentrations in quartz

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Rossman, G.R.; Weis, D.; Wasserburg, G.J.

    1987-09-01

    The concentrations of Rb, Sr, Nd and Sm in quartz crystals from Crystal Peak, Colorado; Steward Mine, California; Tomas Gonzaga, Minas Gerais, Brazil; and Coleman Mines, Arkansas, were determined by isotope dilution mass spectrometry. Concentrations ranged from: 1.17 to 177 ppb Rb; 3.26 to 1027 ppm Sr; 0.0159 to 0.48 ppm Sm; 0.127 to 2.81 ppb Nd. In the Brazilian crystal, concentrations of these elements were correlated with the amount of fluid inclusion water measured visually by turbidity and quantitatively with infrared adsorption spectroscopy. The highest Rb content was found for a crystal free of visible inclusions, indicating that smallmore » amounts of Rb can also occur in quartz itself. Rb and Sr contents are much lower in synthetic quartz grown commercially from the Arkansas quartz.« less

  7. Rb-Sr systematics and REE abundances in Shalka and several other diogenites

    NASA Astrophysics Data System (ADS)

    Takahashi, K.; Yabuki, S.; Kagi, H.; Masuda, A.

    1994-07-01

    The diogenites have been regarded as igneous products in the early solar system and they have been considered to have genetically close relationship with eucrites. Depsite their simple mineralogical compositions and narrow range for major-element compositions, diogenites have been known to show wide Rare Earth Elements (REE) variations in absolute concentration and in mutual abundance ratios. Furthermore, some diogenites have peculiar Rb-Sr isotope systematics (ages younger than 4.5 b.y.). The Shalka meteorite belongs to the diogenites, and a unique REE abundance pattern has been reported. We performed Rb-Sr isotopic analyses and measured REE abundances in the Shalka diogenite with several other diogenites to discuss their genesis. Roughly speaking, REE patterns in diogenites are characterized by the negative Eu anomaly and the depletion of light REE. For Shalka, some heterogeneity in REE abundance patterns have been observed. While one sample chip shows the REE pattern with a large negative Eu anomaly and depleted light REE, particularly characterized by the concave curvature for the La-Nd span, other samples show the pattern nearly flat or the pattern enriched in light REE. These variations could not be explained easily by the simple mixing process of LREE-depleted components and LREE-enriched melt, but they imply some metamorphism process. The Rb-Sr isotopic data for Shalka are shown with the data for other several diogenites. These observations indicate that Shalka would undergo a significant extent of metamorphism followed by redistribution of REE and the disturbance of the Rb-Sr systematics. We are going to do further studies on Shalka to discuss the metamorphic process and compare it with other diogenites.

  8. Mineralogical, Chemical, and Isotopic Heterogeneity in Zagami: Evidence for a Complex Petrogenesis

    NASA Technical Reports Server (NTRS)

    Nyquist, L. E.; Misawa, K.; Shih, C-Y.; Niihara, T.; Park, J.

    2013-01-01

    Textural variations in the shergottite Zagami were initially interpreted as evidence that it formed in a heterogeneous lava flow. Variations in initial Sr-87/Sr-86 ratios between a Coarse Grained (CG) and a Fine Grained (FG) lithology and evidence for more extensive fractionation of the Rb/Sr ratio in a Dark Mottled Lithology (DML) are consistent with such an interpretation. More recently, Niihara et al. and Misawa et al. have reported the mineralogy and Sr-isotopic systematics of an Olivine Rich Lithology (ORL) found in association with the coarse-grained DML lithology in the Kanagawa Zagami specimen [6,7]. Here we call this lithology DML(Ka) to maintain a distinction with DML(USNM) as studied. An Ar-Ar study by Park et al. of a late stage K-rich melt enriched in K2O to approx 7% and intruded into ORL yielded an Ar-Ar age of 202+/0 7 Ma. The present work extends the study of Kanagawa Zagami to Nd-isotopes.

  9. Diode laser based resonance ionization mass spectrometric measurement of strontium-90

    NASA Astrophysics Data System (ADS)

    Bushaw, B. A.; Cannon, B. D.

    1997-10-01

    A diode laser based scheme for the isotopically selective excitation and ionization of strontium is presented. The double-resonance excitation 5s 21S 0→5s5p 3P 1→5s6s 3S 1 is followed by photoionization at 488 nm. The isotope shifts and hyperfine structure in the resonance transitions have been accurately measured for the stable isotopes and 90Sr, with the measurement of the 90Sr shifts using sub-pg samples. Analytical tests, using graphite crucible atomization, demonstrated 90Sr detection limits of 0.8 fg and overall (optical+mass spectrometer) isotopic selectivity of >10 10 against stable strontium.

  10. Geochronological, geochemical and Sr-Nd-Hf isotopic constraints on the petrogenesis of Late Cretaceous A-type granites from the Sibumasu Block, Southern Myanmar, SE Asia

    NASA Astrophysics Data System (ADS)

    Jiang, Hai; Li, Wen-Qian; Jiang, Shao-Yong; Wang, He; Wei, Xiao-Peng

    2017-01-01

    The Late Cretaceous to Paleogene granitoids occur widespread in the Sibumasu block within Myanmar (SE Asia), which show a close association with tin-tungsten mineralization. However, the precise timing, petrogenesis and tectonic significance of these granitoids are poorly constrained so far. In this study, we present a detailed study on geochronology, elemental and Sr-Nd-Hf isotopic geochemistry for the Hermyingyi and Taungphila granites in southern Myanmar, with the aim of determining their petrogenesis and tectonic implications. LA-ICP-MS U-Pb dating of zircon grains from the two granites yield ages of 69-70 Ma, indicating a Late Cretaceous magmatic event. These granitic rocks are weakly peraluminous and belong to the high-K calc-alkaline series. They are both characterized by high SiO2, K2O + Na2O, FeOT/(FeOT + MgO) and Ga/Al ratios and low Al2O3, CaO, MgO, P2O5 and TiO2 contents, enriched in Rb, Th, U and Y, but depleted in Ba, Sr, P, and Eu, suggesting an A-type granite affinity. Moreover, they display prominent tetrad REE patterns and non-CHARAC trace element behavior, which are common in late magmatic differentiates with strong hydrothermal interaction or deuteric alteration. The granites belong to A2-type and probably formed at a high temperature and anhydrous condition. They have zircon εHf(t) values from - 12.4 to - 10.0 and whole-rock εNd(t) values from - 11.3 to - 10.6, with Paleoproterozoic TDM2 ages (1741-1922 Ma) for both Hf and Nd isotopes. Geochemical and isotopic data suggest that these A-type granites were derived from partial melting of the Paleoproterozoic continental crust dominated by metaigneous rocks with tonalitic to granodioritic compositions, without significant input of mantle-derived magma and followed by subsequent fractional crystallization. By integrating all available data for the regional tectonic evolution in SE Asia and adjacent regions, we attribute the formation of the Late Cretaceous A-type granites to a back-arc extension

  11. A preliminary bioavailable strontium isotope soil map of Europe.

    NASA Astrophysics Data System (ADS)

    Hoogewerff, Jurian; Reimann, Clemens; Ueckermann, Henriette; Frei, Robert; Frei, Karin; van Aswegen, Thalita; Stirling, Claudine; Reid, Malcolm; Clayton, Aaron; Gemas Project Team

    2017-04-01

    The GEMAS project collected samples from grazing land (n=2118, 0-20cm depth) and agricultural soil (n=2211, 0-10cm depth) at a scale of 1 site/2500km2 in most of Europe1. Elemental analysis using different extractions (Aqua Regia and MMI), whole soil XRF data and Q-ICPMS lead isotope data have been published1. Here we report high-precision 87Sr/86Sr results for the first 1000+ samples. To best represent Sr in plants and animals an ammonium nitrate soil extraction was chosen2. Samples were measured in three laboratories and shared QC samples demonstrated the robustness of the complete extraction and measurement protocol. Observed 87Sr/86Sr values range from 0.7038 to 0.7597 with the majority of samples centring about the median of 0.7092. Spatial interpolation of the data shows some major trends over Europe with high 87Sr/86Sr in known old intrusive terrains in Scandinavia, Iberia and the Alps. To improve the spatial resolution we investigated relations between measured 87Sr/86Sr values and other parameters for which higher spatial density (interpolated) data exists in geological and lithological databases like IGME50003 and GLiM4. For each sampling site matching geological age data and lithology were obtained by overlaying sampling locations on the IGME5000 and GLiM maps and extracting age and lithology information. All statistical and geospatial manipulations were performed using the R statistical package. Overall the 87Sr/86Sr values show a moderate correlation (Pearson R=0.54) with age but demonstrate varying homogeneity in different lithological units. Within the GEMAS dataset the strontium isotope ratios correlate most strongly with the lead isotope results,206Pb/208Pb (R=0.56) indicating a combined age and "crustalinity" effect. Whole soil Rb (XRF) is slightly higher correlated (R=0.26) with 87Sr/86Sr than extracted Rb (AR) at R=0.12 indicating some influence of the long term Rb signal in the soil parent material. Sodium is the highest correlated whole soil

  12. Modeling secular changes in seawater chemistry accurately requires inclusion of environmental controls on low-temperature, off-axis, hydrothermal fluxes

    NASA Astrophysics Data System (ADS)

    Coogan, L. A.; Dosso, S. E.; Higgins, J. A.

    2014-12-01

    There are sharp rises in the Sr- and Li-isotopic composition of seawater at the Eocene-Oligocene boundary that are generally thought to be associated with Himalayan uplift and associated climatic changes and continental weathering variability. In modeling such data the norm is to hold the chemical fluxes associated with off-axis hydrothermal circulation through the oceanic crust constant while varying the river fluxes (and/or isotopic ratios). There is, however, no a priori reason to assume the chemical fluxes (or isotopic compositions) associated with off-axis hydrothermal systems should stay constant. Instead, changing environmental conditions (e.g. seawater composition and bottom water temperature) will lead to changes in these fluxes. An alternative model to explain the sharp rise in the Sr- and Li-isotopic composition of seawater at the Eocene-Oligocene boundary is cooling of the deep ocean. Decreased reaction rates in the oceanic crust, due to decreasing temperature, can be shown to lead to a decrease in the flux of unradiogenic Sr into the ocean. The magnitude matches, within uncertainty, that required to explain the increase in seawater Sr-isotopic composition [Coogan and Dosso, in review]. The story for Li is more uncertain. Two factors may lead to smaller effective fractionation factors between seawater and the (large) Li sink in the oceanic crust when bottom water is warmer: (i) higher temperature will decrease the isotopic fractionation factor; (ii) the more extensive fluid-rock reaction in the ocean crust when bottom water is warmer will make Li uptake by the oceanic crust more efficient. All other things being equal this will lead to a lower Li content of seawater. In turn, a lower Li content in seawater will mean that for a given Li-uptake rate by the crust the effective fractionation factor is smaller, due to Rayleigh distillation of Li-isotopes during fluid-rock reaction in the oceanic crust. In combination these factors predict a significant (many

  13. Sm-Nd in marine carbonates and phosphates - Implications for Nd isotopes in seawater and crustal ages

    NASA Technical Reports Server (NTRS)

    Shaw, H. F.; Wasserburg, G. J.

    1985-01-01

    The possibility of establishing a record of variations in the isotopic composition of Nd in seawater over geologic time is explored. To construct such a record, a phase must be identified which incorporated Nd with the same isotopic composition as seawater at the time of its formation, preserves that composition, and which is relatively common in sediments. To evaluate the suitability of carbonates and phosphates, the Rb, Sr, Sm, and Nd concentrations and the Nd and Sr isotopic composition of a variety of modern and ancient marine calcite, aragonite, and apatite samples have been measured and the results are presented and discussed.

  14. Strontium isotopic study of subsurface brines from Illinois basin

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    hetherington, E.A.; Stueber, A.M.; Pushkar, P.

    1986-05-01

    The abundance of the radiogenic isotope /sup 87/Sr in a subsurface brine can be used as a tracer of brine origin, evolution, and diagenetic effects. The authors have determined the /sup 87/Sr//sup 86/Sr ratios of over 60 oil-field waters from the Illinois basin, where brine origin is perplexing because of the absence of any significant evaporite strata. Initially, they analyzed brines from 15 petroleum-producing sandstone and carbonate units; waters from Ordovician, Silurian, Devonian, and Mississippian strata have /sup 87/Sr//sup 86/Sr ratios in the range 0.7079-0.7108. All but those from the Ste. Genevieve Limestone (middle Mississippian) are more radiogenic in /supmore » 87/Sr//sup 86/Sr than seawater values for this interval of geologic time. The detrital source of the more radiogenic /sup 87/Sr may be the New Albany Shale group, considered to be a major petroleum source rock in the basin. The /sup 87/Sr//sup 86/Sr ratios of Ste. Genevieve brines apparently evolved without a contribution from fluid-shale interaction.« less

  15. Micaschist and Impure Marble - two Examples for Lithology Related Constraints to Rb-Sr Microsampling Analysis

    NASA Astrophysics Data System (ADS)

    Wegmann, M. I.; Hammerschmidt, K.

    2003-12-01

    Retrograde overprinted calcite-bearing micaschists and mica-containing marbles from the northern part of the Cycladic blueschist belt on South-Evia, Greece, have been investigated to understand the interplay between bulk rock chemistry, mineral assemblage and resetting of the Rb-Sr isotope system during deformation. White mica represents two optical distinguishable microstructures, isoclinal folds (S1) and axial plain cleavage (S2) induced by flattening and elongation episode of isothermal exhumation. The varying Si content of phengites is not related to microstructures. Due to microstructural complexity and grain size variation the application of Rb-Sr microsampling method was expected effective investigation of Rb and Sr rich mineral phases to elucidate constraints for geochronological and isotope geochemical imprint in microstructures. Drilling out calcite, albite and mica samples with weights down to 200æg each out of 30æm thick sections realized textural controlled separation. Calculated Rb-Sr mica ages show lithology-related scattering but totally not microstructural induced variation. Particulary, S1 and S2 phengites in micaschist yield similar age values around 31 Ma. In contrast, impure marble mica within similar S1 and S2 have Rb-Sr mica ages widely scattering between 34 and 50 Ma. Therefore, structural elements formed by these phengites are not distinguishable in terms of geochronolgy. Explaining the scatter of age values, principally, two possibilities were taken into account, (i) the fluid flux neccessary to homogenize Sr isotope composition in mica and calcite (albite) might have been less effective in impure marble than in micaschist due to the generation of CO2. In constrast to this possibility, calcite 87Sr/86Sr in both specimen are quite homogeneous at least on cm-scale, e.g. values of 0.712125 ñ 66 (2s) for impure marble and of 0.721419 ñ 42 for micaschist were meassured. Albite 87Sr/86Sr corroborate Sr homogenisation on scale this study was

  16. VARIATIONS IN ISOTOPIC ABUNDANCES OF STRONTIUM, CALCIUM, AND ARGON AND RELATED TOPICS. Eleventh Annual Progress Report for 1963

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    None

    1963-12-01

    Separate abstracts were prepared for twenty-eight of the thirty-three papers. The other papers deal with whole-rock Rb- Sr ages of Ontario norite and micropegmatite and the Southern Rhodesia Great Dyke, Sr isotopes in vein type mineral deposits, whole-rock Rb-- Sr studies of volcanics, and accuracy in Sr / sup 87//Sr/sup 86/ measurements. (D.C.W.)

  17. Late Eocene to present isotopic (Sr-Nd-Pb) and geochemical evolution of sediments from the Lomonosov Ridge, Arctic Ocean: Implications for continental sources and linkage with the North Atlantic Ocean

    NASA Astrophysics Data System (ADS)

    Stevenson, Ross; Poirier, André; Véron, Alain; Carignan, Jean; Hillaire-Marcel, Claude

    2015-09-01

    New geochemical and isotopic (Sr, Nd, Pb) data are presented for a composite sedimentary record encompassing the past 50 Ma of history of sedimentation on the Lomonosov Ridge in the Arctic Ocean. The sampled sediments encompass the transition of the Arctic basin from an enclosed anoxic basin to an open and ventilated oxidized ocean basin. The transition from anoxic basin to open ventilated ocean is accompanied by at least three geochemical and isotopic shifts and an increase in elements (e.g., K/Al) controlled by detrital minerals highlighting significant changes in sediment types and sources. The isotopic compositions of the sediments prior to ventilation are more variable but indicate a predominance of older crustal contributions consistent with sources from the Canadian Shield. Following ventilation, the isotopic compositions are more stable and indicate an increased contribution from younger material consistent with Eurasian and Pan-African crustal sources. The waxing and waning of these sources in conjunction with the passage of water through Fram Strait underlines the importance of the exchange of water mass between the Arctic and North Atlantic Oceans.

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

    PubMed

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

    2015-05-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2010-05-01

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

  20. A novel procedure for Rubidium separation and its isotope measurements on geological samples by MC-ICP-MS

    NASA Astrophysics Data System (ADS)

    Ma, J.; Zhang, Z.; Wei, G.; Zhang, L.

    2017-12-01

    A method including a novel column Rb separation procedure and high-precision Rb isotope measurement in geological materials by using multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) in standard-sample-bracketing (SSB) mode has been developed. Sr-Spec resin was employed, in which the distribution coefficients for Rb, K, Ba and Sr are different in nitric acid, to sequentially separate them from the matrix. The dissolved samples were loaded on the column in 3 M HNO3, the main matrix such as Al, Ca, Fe, Mg, Mn and Na were removed by rinsing with 4.5 mL HNO3, Rb and K were then sequentially eluted by 3 M HNO3 in different volumes. After that, Ba was eluted by 8 M HNO3, and Sr was finally eluted by Milli-Q water. This enable us to collect the pure Rb, K, Ba and Sr one by one with recovery close to 100% for their isotopic compositions measurement on MC-ICP-MS. We here focus on Rb isotope measurement. The measurement using MC-ICP-MS yielded an internal precision for δ87Rb of < ± 0.03‰ (2SE), and the external precision was generally better than ± 0.06‰ (2SD) based on the long-term results of the Rb standard solutions NIST SRM 984. A series of geological rock standards, were analyzed using this method, and the results indicate significant Rb isotope differences in different geologic materials. This will provide a powerful tool to investigate Rb isotope fractionation during geological processes.Based on this method, Rb isotope compositions from a basaltic weathering profile were carried out. The data show the lighter Rb (85Rb) isotope is preferentially leached from the weathering profile and remains heavy Rb isotope (87Rb) in the weathered residues during the incipient weathering stage. From the moderate to advanced weathering stage, the significant variations of Rb isotope were observed and multiple factors, such as leaching, adsorption, desorption, and precipitation, should play important role in fractionating Rb isotope.

  1. The chemical and isotopic differentiation of an epizonal magma body: Organ Needle pluton, New Mexico

    USGS Publications Warehouse

    Verplanck, P.L.; Farmer, G.L.; McCurry, M.; Mertzman, S.A.

    1999-01-01

    Major and trace element, and Nd and Sr isotopic compositions of whole rocks and mineral separates from the Oligocene, alkaline Organ Needle pluton (ONP), southern New Mexico, constrain models for the differentiation of the magma body parental to this compositionally zoned and layered epizonal intrusive body. The data reveal that the pluton is rimmed by lower ??(Nd) (~-5) and higher 87Sr/86Sr (~0.7085) syenitic rocks than those in its interior (??(Nd) ~ 2, 87Sr/86Sr ~0.7060) and that the bulk compositions of the marginal rocks become more felsic with decreasing structural depth. At the deepest exposed levels of the pluton, the ??(Nd)~-5 lithology is a compositionally heterogeneous inequigranular syenite. Modal, compositional and isotopic data from separates of rare earth element (REE)-bearing major and accesory mineral phases (hornblende, titanite, apatite, zircon) demonstrate that this decoupling of trace and major elements in the inequigranular syenite results from accumulation of light REE (LREE)-bearing minerals that were evidently separated from silicic magmas as the latter rose along the sides of the magma chamber. Chemical and isotopic data for microgranular mafic enclaves, as well as for restite xenoliths of Precambrian granite wall rock, indicate that the isotopic distinction between the marginal and interior facies of the ONP probably reflects assimilation of the wall rock by ??(Nd) ~-2 mafic magmas near the base of the magma system. Fractional crystallization and crystal liquid separation of the crystally contaminated magma at the base and along the margins of the chamber generated the highly silicic magmas that ultimately pooled at the chamber top.

  2. Coal fly ash interaction with environmental fluids: Geochemical and strontium isotope results from combined column and batch leaching experiments

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Brubaker, Tonya M; Stewart, Brian W; Capo, Rosemary C

    2013-05-01

    The major element and Sr isotope systematics and geochemistry of coal fly ash and its interactions with environmental waters were investigated using laboratory flow-through column leaching experiments (sodium carbonate, acetic acid, nitric acid) and sequential batch leaching experiments (water, acetic acid, hydrochloric acid). Column leaching of Class F fly ash samples shows rapid release of most major elements early in the leaching procedure, suggesting an association of these elements with soluble and surface bound phases. Delayed release of certain elements (e.g., Al, Fe, Si) signals gradual dissolution of more resistant silicate or glass phases as leaching continues. Strontium isotope resultsmore » from both column and batch leaching experiments show a marked increase in {sup 87}Sr/{sup 86}Sr ratio with continued leaching, yielding a total range of values from 0.7107 to 0.7138. For comparison, the isotopic composition of fluid output from a fly ash impoundment in West Virginia falls in a narrow range around 0.7124. The experimental data suggest the presence of a more resistant, highly radiogenic silicate phase that survives the combustion process and is leached after the more soluble minerals are removed. Strontium isotopic homogenization of minerals in coal does not always occur during the combustion process, despite the high temperatures encountered in the boiler. Early-released Sr tends to be isotopically uniform; thus the Sr isotopic composition of fly ash could be distinguishable from other sources and is a useful tool for quantifying the possible contribution of fly ash leaching to the total dissolved load in natural surface and ground waters.« less

  3. Radiogenic isotope evidence for transatlantic atmospheric dust transport

    NASA Astrophysics Data System (ADS)

    Kumar, Ashwini; Abouchami, Wafa; Garrison, Virginia H.; Galer, Stephen J. G.; Andreae, Meinrat O.

    2013-04-01

    Early studies by Prospero and colleagues [1] have shown that African dust reaches all across the Atlantic and into the Caribbean. It may contribute to fertilizing the Amazon rainforest [2,3,4], in addition to enhancing the ocean biological productivity via delivery of iron, a key nutrient element[5]. Radiogenic isotope ratios (Sr, Nd, Pb) are robust tracers of dust sources and can thus provide information on provenance and pathways of dust transport. Here we report Sr, Nd and Pb isotope data on atmospheric aerosols, collected in 2008 on quartz filters, from three different locations in Mali (12.6° N, 8.0° W; 555 m a.s.l.), Tobago (11.3° N, 60.5° W; 329 m a.s.l.) and the U.S. Virgin Islands (17.7° N, 64.6° W; 27 m a.s.l.) to investigate the hypothesis of dust transport across the Atlantic. About 2 cm2 of filter were acid-leached in 0.5 N HBr for selective removal of the anthropogenic labile Pb component (leachate) and possibly the fine soluble particle fraction. The remainder of the filter was subsequently dissolved using a mixture of HF and HNO3 acids, and should be representative of the silicate fraction. Isotopic compositions were measured by TIMS on a ThermoFisher Triton at MPIC, with Pb isotope ratios determined using the triple-spike method. Significant Pb isotope differences between leachates and residues were observed. The variability in Pb isotopic composition among leachates may be attributed to variable and distinct anthropogenic local Pb sources from Africa and South America [6], however, residues are imprinted by filter blank contribution suggesting to avoid the quartz fiber filter for isotopic study of aerosols. The Nd and Sr isotope ratios of aerosol leachates show similar signatures at all three locations investigated. The nearly identical Nd and Sr isotopic compositions in the Mali, Tobago and Virgin islands leachates are comparable to those obtained on samples from the Bodélé depression, Northern Chad [7] and suggest a possible common

  4. Potential application of radiogenic isotopes and geophysical methods to understand the hydrothermal dystem of the Upper Geyser Basin, Yellowstone National Park

    USGS Publications Warehouse

    Paces, James B.; Long, Andrew J.; Koth, Karl R.

    2015-01-01

    Numerous geochemical and geophysical studies have been conducted at Yellowstone National Park to better understand the hydrogeologic processes supporting the thermal features of the Park. This report provides the first 87Sr/86Sr and 234U/238U data for thermal water from the Upper Geyser Basin (UGB) intended to evaluate whether heavy radiogenic isotopes might provide insight to sources of groundwater supply and how they interact over time and space. In addition, this report summarizes previous geophysical studies made at Yellowstone National Park and provides suggestions for applying non-invasive ground and airborne studies to better understand groundwater flow in the subsurface of the UGB. Multiple samples from Old Faithful, Aurum, Grand, Oblong, and Daisy geysers characterized previously for major-ion concentrations and isotopes of water (δ2H, δ18O, and 3H) were analyzed for Sr and U isotopes. Concentrations of dissolved Sr and U are low (4.3–128 ng g-1 Sr and 0.026–0.0008 ng g-1 U); consequently only 87Sr/86Sr data are reported for most samples. Values of 87Sr/86Sr for most geysers remained uniform between April and September 2007, but show large increases in all five geysers between late October 2007 and early April, 2008. By late summer of 2008, 87Sr/86Sr values returned to values similar to those observed a year earlier. Similar patterns are not present in major-ion data measured on the same samples. Furthermore, large geochemical differences documented between geysers are not observed in 87Sr/86Sr data, although smaller differences between sites may be present. Sr-isotope data are consistent with a stratified hydrologic system where water erupted in spring and summer of 2007 and summer of 2008 equilibrated with local intracaldera rhyolite flows at shallower depths. Water erupted between October 2007 and April 2008 includes greater amounts of groundwater that circulated deep enough to acquire a radiogenic 87Sr/86Sr, most likely from Archean basement

  5. Using Isotopes to Reconstruct Mammalian Diet, Migration and Paleoenvironment for Hominin Sites in Indonesia

    NASA Astrophysics Data System (ADS)

    Wershow, H.; Janssen, R.; Vonhof, H.; Lubbe, J. V. D.; Joordens, J. J.; Koutamanis, D. S.; Puspaningrum, M. R.; de Vos, J.; Reijmer, J.

    2015-12-01

    Climate plays a prominent role in ecosystem development in the biodiversity hotspot Sundaland (Malaysia and western Indonesia) throughout the Quaternary. Recurrent isolation and connection of the islands to mainland Asia due to sea level fluctuations has enabled repeated biotic migrations and encouraged genetic speciation. These migration waves also brought Homo erectus to Java. Together with extensive and well-documented collections of other terrestrial species, these hominin fossils form faunal assemblages of which the paleoenvironmental and paleogeographical background is poorly known. Using carbon, oxygen and strontium isotopes, we have reconstructed the paleoenvironmental and paleoecological conditions of several Holocene and Pleistocene fossil sites on Sumatra and Java, Indonesia. Carbon (∂13C) and oxygen (∂18O) isotope analysis of well-preserved herbivore teeth enamel reveals a marked contrast between C3-dominated diets in warmer periods, and C4-dominated diets in cooler periods, reflecting the distinct changes in Sundaland vegetation cover between glacials and interglacials. These isotope patterns allow us to assign the appropriate climatic background to some of the older fossil assemblages from Java, for which dating uncertainty does not allow direct assignment to glacial or interglacial conditions. The stable isotope signatures of herbivores from Trinil and Sangiran, sites well-known for the fossil occurrence of Homo erectus, indicate glacial conditions. The isotope data of several H. erectus fossils from these sites seem to be in line with such an interpretation. Furthermore, we applied strontium (87Sr/86Sr) isotope analyses to a sample subset. The preliminary data show distinct Sr-isotope ratios for different sites, providing clues for the applicability of this isotope technique in detecting climate-related mobility of Sundaland fossil faunas.

  6. Identifying the origins of local atmospheric deposition in the steel industry basin of Luxembourg using the chemical and isotopic composition of the lichen Xanthoria parietina.

    PubMed

    Hissler, Christophe; Stille, Peter; Krein, Andreas; Geagea, Majdi Lahd; Perrone, Thierry; Probst, Jean-Luc; Hoffmann, Lucien

    2008-11-01

    Trace metal atmospheric contamination was assessed in one of the oldest European industrial sites of steel production situated in the southern part of the Grand-Duchy of Luxembourg. Using elemental ratios as well as Pb, Sr, and Nd isotopic compositions as tracers, we found preliminary results concerning the trace metal enrichment and the chemical/isotopic signatures of the most important emission sources using the lichen Xanthoria parietina sampled at 15 sites along a SW-NE transect. The concentrations of these elements decreased with increasing distance from the historical and actual steel-work areas. The combination of the different tracers (major elements, Rare Earth Element ratios, Pb, Sr and Nd isotopes) enabled us to distinguish between three principal sources: the historical steel production (old tailings corresponding to blast-furnace residues), the present steel production (industrial sites with arc electric furnace units) and the regional background (baseline) components. Other anthropogenic sources including a waste incinerator and major roads had only weak impacts on lichen chemistry and isotopic ratios. The correlation between the Sr and Nd isotope ratios indicated that the Sr-Nd isotope systems represented useful tools to trace atmospheric emissions of factories using scrap metal for steel production.

  7. The 87Sr/86Sr ratios of lacustrine carbonates and lake-level history of the Bonneville paleolake system

    USGS Publications Warehouse

    Hart, W.S.; Quade, Jay; Madsen, D.B.; Kaufman, D.S.; Oviatt, Charles G.

    2004-01-01

    Lakes in the Bonneville basin have fluctuated dramatically in response to changes in rainfall, temperature, and drainage diversion during the Quaternary. We analyzed tufas and shells from shorelines of known ages in order to develop a relation between 87Sr/86Sr ratio of carbonates and lake level, which then can be used as a basis for constraining lake level from similar analyses on carbonates in cores. Carbonates from the late Quaternary shorelines yield the following average 87Sr/86Sr ratios: 0.71173 for the Stansbury shoreline (22-20 14C ka; 1350 m), 0.71153 for the Bonneville shoreline (15.5-14.5 14C ka; 1550 m), 0.71175 for the Provo shoreline (14.4-14.0 14C ka; 1450 m), 0.71244 for the Gilbert shoreline (???10.3-10.9 14C ka; 1300 m), and 0.71469 for the modern Great Salt Lake (1280 m). These analyses show that the 87Sr/86Sr ratio of lacustrine carbonates changes substantially at low- to mid-lake levels but is invariant at mid- to high-lake levels. Sr-isotope mixing models of Great Salt Lake and the Bonneville paleolake system were constructed to explain these variations in 87Sr/86Sr ratios with change in lake level. Our model of the Bonneville system produced a 87Sr/86Sr ratio of 0.71193, very close to the observed ratios from high-shoreline tufa and shell. The model verifies that the integration of the southern Sevier and Beaver rivers with the Bear and others rivers in the north is responsible for the lower 87Sr/86Sr ratios in Lake Bonneville compared to the modern Great Salt Lake. We also modeled the 87Sr/86Sr ratio of Lake Bonneville with the upper Bear River diverted into the Snake River basin and obtained an 87Sr/86Sr ratio of 0.71414. Coincidentally, this ratio is close to the observed ratio for Great Salt Lake of 0.71469. This means that 87Sr/86Sr ratios of >0.714 for carbonate can be produced by climatically induced low-lake conditions or by diversion of the upper Bear River out of the Bonneville basin. This model result also demonstrates that the

  8. Can stable isotopes and radiocarbon dating provide a forensic solution for curbing illegal harvesting of threatened cycads?

    PubMed

    Retief, Kirsten; West, Adam G; Pfab, Michèle F

    2014-11-01

    Cycads in South Africa are facing an extinction crisis due to the illegal extraction of plants from the wild. Proving wild origin of suspect ex situ cycads to the satisfaction of a court of law is difficult, limiting law enforcement efforts. We investigated the feasibility of using multiple stable isotopes to identify specimens removed from the wild. Relocated and wild specimens from two species in the African genus Encephalartos (E. lebomboensis and E. arenarius) were sampled. (14) C analysis indicated that a ± 30-year chronology could be reliably obtained from the cycads. For E. arenarius, pre-relocation tissue was consistent with a wild origin, whereas tissue grown post-relocation was isotopically distinct from the wild for (87) Sr/(86) Sr and δ(15) N. For E. lebomboensis, δ(34) S, δ(18) O, and (87) Sr/(86) Sr were different between relocated and control plants, consistent with the >30 years since relocation. Our findings demonstrate the potential for a forensic isotope approach to identify illegal ex situ cycads. © 2014 American Academy of Forensic Sciences.

  9. Elemental and Sr-Nd isotopic geochemistry of Cretaceous to Early Paleogene granites and volcanic rocks in the Sikhote-Alin Orogenic Belt (Russian Far East): implications for the regional tectonic evolution

    NASA Astrophysics Data System (ADS)

    Zhao, Pan; Jahn, Bor-ming; Xu, Bei

    2017-09-01

    The Sikhote-Alin Orogenic Belt in Russian Far East is an important Late Mesozoic to Early Cenozoic accretionary orogen related to the subduction of the Paleo-Pacific Plate. This belt was generated by successive accretion of terranes made of accretionary prisms, turbidite basins and island arcs to the continental margin of northeastern Asia (represented by the Bureya-Jiamusi-Khanka Block) from Jurassic to Late Cretaceous. In order to study the tectonic and crustal evolution of this orogenic belt, we carried out zircon U-Pb dating, and whole-rock elemental and Sr-Nd isotopic analyses on granites and volcanic rocks from the Primorye region of southern Sikhote-Alin. Zircon dating revealed three episodes of granitoid emplacement: Permian, Early Cretaceous and Late Cretaceous to Early Paleogene. Felsic volcanic rocks (mainly rhyolite, dacite and ignimbrite) that overlay all tectonostratigraphic terranes were erupted during 80-57 Ma, postdating the accretionary process in the Sikhote-Alin belt. The Cretaceous-Paleogene magmatism represents the most intense tectonothermal event in the Sikhote-Alin belt. Whole-rock major and trace elemental data show arc-like affinity for granitoids and volcanic rocks, indicating that they were likely generated in a supra-subduction setting. Their initial 87Sr/86Sr ratios range from 0.7048 to 0.7114, and εNd(t) values vary from +1.7 to -3.8 (mostly < 0). Thus, the elemental and Sr-Nd isotopic data suggest that the felsic magmas were generated by partial melting of source rocks comprising mantle-derived juvenile component and recycled crustal component. In addition to the occurrence in the Sikhote-Alin orogenic belt, Cretaceous to Early Paleogene magmatic rocks are also widespread in NE China, southern Korean peninsula, Japanese islands and other areas of Russian Far East, particularly along the coastal regions of the Okhotsk and Bering Seas. These rocks constitute an extended magmatic belt along the continental margin of NE Asia. The

  10. DEPENDENCE OF THE Sr-TO-Ba AND Sr-TO-Eu RATIO ON THE NUCLEAR EQUATION OF STATE IN METAL-POOR HALO STARS

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Famiano, M. A.; Kajino, T.; Aoki, W.

    A model is proposed in which the dependence on the equation of state (EOS) of the scatter of [Sr/Ba] in metal-poor stars is studied. Light r-process element enrichment in these stars has been explained via a truncated r-process, or “tr-process.” The truncation of the r-process from a generic core-collapse event followed by a collapse into an accretion-induced black hole is examined in the framework of a galactic chemical evolution model. The constraints on this model imposed by observations of extremely metal-poor stars are explained, and the upper limits in the [Sr/Ba] distributions are found to be related to the nuclearmore » EOS in a collapse scenario. The scatter in [Sr/Ba] and [Sr/Eu] as a function of metallicity has been found to be consistent with turbulent ejection in core-collapse supernovae. Adaptations of this model are evaluated to account for the scatter in isotopic observables. This is done by assuming mixing in ejecta in a supernova event. Stiff EOS are eliminated by this model.« less

  11. Geochemistry, isotopic composition (δ 18O, δ 2H, 87Sr/ 86Sr, 143Nd/ 144Nd) in the groundwater of French Guiana as indicators of their origin, interrelations

    NASA Astrophysics Data System (ADS)

    Négrel, Philippe; Petelet-Giraud, Emmanuelle

    2010-10-01

    The current use of untreated river water for drinking purposes by the population of French Guiana has important impacts on public health. Consequently, groundwater is of major importance as a possible alternative drinking water supply to reduce these impacts. Since French Guiana belongs to the Guyana Shield, sustainable water management can be expected to depend increasingly on water from fissured aquifers in hard rocks. Groundwater samples were collected from shallow drill holes in the densely populated coastal area, and deeper wells in the basement (around Cayenne and along the Maroni and Oyapock rivers). This study reports on major and trace elements for which Na + and Ca 2+ excess with regard to Cl reflect the role of water-rock interaction, as well as Sr and Nd isotopes that reflect the role of the different lithologies. δ 18O and δD in waters give constraints on the water cycle (recharge and evaporation processes).

  12. Isotopic decoupling during porous melt flow: A case-study in the Lherz peridotite

    NASA Astrophysics Data System (ADS)

    Le Roux, V.; Bodinier, J.-L.; Alard, O.; O'Reilly, S. Y.; Griffin, W. L.

    2009-03-01

    Most peridotite massifs and mantle xenoliths show a wide range of isotopic variations, often involving significant decoupling between Hf, Nd and Sr isotopes. These variations are generally ascribed either to mingling of individual components of contrasted isotopic compositions or to time integration of parent-element enrichment by percolating melts/fluids, superimposed onto previous depletion event(s). However, strong isotopic decoupling may also arise during porous flow as a result of daughter-elements fractionation during solid-liquid interaction. Although porous flow is recognized as an important process in mantle rocks, its effects on mantle isotopic variability have been barely investigated so far. The peridotites of the Lherz massif (French Pyrenees) display a frozen melt percolation front separating highly refractory harzburgites from refertilized lherzolites. Isotopic signatures observed at the melt percolation front show a strong decoupling of Hf from Nd and Sr isotopes that cannot be accounted for by simple mixing involving the harzburgite protolith and the percolating melt. Using one dimensional percolation-diffusion and percolation-reaction modeling, we show that these signatures represent transient isotopic compositions generated by porous flow. These signatures are governed by a few critical parameters such as daughter element concentrations in melt and peridotite, element diffusivity, and efficiency of isotopic homogenization rather than by the chromatographic effect of melt transport and the refertilization reaction. Subtle variations in these parameters may generate significant inter-isotopic decoupling and wide isotopic variations in mantle rocks.

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

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

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

  14. Ca isotopes in the Ebro River Basin: mixing and lithological tracer

    NASA Astrophysics Data System (ADS)

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

    2012-12-01

    A large investigation of the Ebro River catchment was done in the past years regarding hydrogen, oxygen, lithium, boron, sulphur and oxygen from SO4 and strontium isotope measurements together with major and trace elements in the dissolved load of 25 river samples collected within the Ebro River Basin in Spain (Millot et al., Geophysical Research Abstracts, Vol. 14, EGU2012-2062, 2012). The Ebro River (928 km long, 85,530 km2 drainage basin) located in North-Eastern Spain rises near the Atlantic coast in the Cantabrian Mountains and flows into the western Mediterranean Sea through several large cities and agricultural, mining and industrial areas. The river is one of the largest contributors of freshwater in the Mediterranean Sea and ends in the Ebro delta, one of the most important wetlands in Europe. Bedrocks of the Ebro River Basin are mainly dominated by carbonates and evaporites from the Paleozoic and Mesozoic terrains. The Ebro river mainstream was sampled at Amposta one time per month between June 2005 and May 2006 and secondly, the Ebro River along its main course and its main tributaries were sampled during one field campaign in April 2006. The behaviour of Ca and its isotopes during water/rock interactions at the scale of a large river basin having various lithologies will be investigated in addition with Sr, S (SO4) and O (SO4) isotopes. One objective is to characterize the processes controlling the isotope signatures of a large river draining predominantly sedimentary bedrocks. The δ44Ca ratio (δ44/40 normalised to Seawater) ranged between -0.87 and -1.09‰ along the Ebro main stream, increasing towards the delta as the Ca content increase. In Amposta, the δ44Ca ratio ranged between -0.66 and -1.04‰ and tends to decrease with the increasing discharge. These variations are very similar to those given by the 87Sr/86Sr ratios and Sr contents. For the tributaries, the δ44Ca ratio ranged between -0.43 and -1.04‰ whereas the anhydrite-gypsum bedrock

  15. Emplacement ages, geochemical and Sr-Nd-Hf isotopic characterization of Mesozoic to early Cenozoic granitoids of the Sikhote-Alin Orogenic Belt, Russian Far East: Crustal growth and regional tectonic evolution

    NASA Astrophysics Data System (ADS)

    Jahn, Bor-ming; Valui, Galina; Kruk, Nikolai; Gonevchuk, V.; Usuki, Masako; Wu, Jeremy T. J.

    2015-11-01

    The Sikhote-Alin Range of the Russian Far East is an important accretionary orogen of the Western Pacific Orogenic Belt. In order to study the formation and tectonic evolution of the orogen, we performed zircon U-Pb dating, as well as geochemical and Sr-Nd-Hf isotopic analyses on 24 granitoid samples from various massifs in the Primorye and Khabarovsk regions. The zircon dating revealed that the granitoids were emplaced from 131 to 56 Ma (Cretaceous to Paleogene). In the Primorye Region, granitoids in the coastal Sikhote-Alin intruded the Cretaceous Taukha Accretionary Terrane from ca. 90 to 56 Ma, whereas those along the Central Sikhote-Alin Fault zone intruded the Jurassic Samarka Accretionary Terrane during ca. 110-75 Ma. The "oldest" monzogranite (131 Ma) was emplaced in the Lermontovka area of the NW Primorye Region. Granitoid massifs along the Central Sikhote-Alin Fault zone in the Khabarovsk Region formed from 109 to 58 Ma. Thus, the most important tectonothermal events in the Sikhote-Alin orogen took place in the Cretaceous. Geochemical analysis indicates that most samples are I-type granitoids. They have initial 87Sr/86Sr ratios ranging from 0.7040 to 0.7083, and initial Nd isotopic ratios, expressed as εNd(t) values, from +3.0 to -5.0 (mostly 0 to -5). The data suggest that the granitoid magmas were generated by partial melting of sources with mixed lithologies, including the subducted accretionary complex ± hidden Paleozoic-Proterozoic basement rocks. Based on whole-rock Nd isotopic data, we estimated variable proportions (36-77%) of juvenile component (=mantle-derived basaltic rocks) in the generation of the granitic magmas. Furthermore, zircon Hf isotopic data (εHf(t) = 0 to +15) indicate that the zircon grains crystallized from melts of mixed sources and that crustal assimilation occurred during magmatic differentiation. The quasi-continuous magmatism in the Sikhote-Alin orogen suggests that the Paleo-Pacific plate subduction was very active in the

  16. In situ strontium and sulfur isotope investigation of the Ni-Cu-(PGE) sulfide ore-bearing Kevitsa intrusion, northern Finland

    NASA Astrophysics Data System (ADS)

    Luolavirta, Kirsi; Hanski, Eero; Maier, Wolfgang; Lahaye, Yann; O'Brien, Hugh; Santaguida, Frank

    2018-01-01

    The 2.06-Ga Kevitsa mafic-ultramafic intrusion in northern Finland hosts a large disseminated Ni-Cu-PGE deposit. The deposit occurs in the ultramafic olivine-pyroxene cumulates and shows a range in Ni tenors varying from 4-7 wt% (regular ore) to > 10 wt% (Ni-PGE ore). There are also a metal-poor sulfide mineralization (false ore) and contact mineralization that are uneconomic (Ni tenor < 4 wt%). The obtained 87Sr/86Sr(i) values of the Kevitsa ultramafic cumulates are highly radiogenic (> 0.7045) in comparison to the estimated depleted mantle Sr isotope ratio of 0.702 at 2.06 Ga. The sulfur δ 34S values are generally higher than + 2‰, which together with the Sr isotope data imply involvement of crustal material in the genesis of the Kevitsa intrusion and its ores. The 87Sr/86Sr(i) values obtained from the ore-bearing domain of the intrusion show stratigraphic variation and exceed 0.7050, with the maximum value reaching up to 0.7109. In contrast, in rocks around the ore domain, the initial Sr isotope compositions remain more or less constant (0.7047-0.7060) throughout the intrusive stratigraphy. The isotope data suggest that the ore-bearing domain of the intrusion represents a dynamic site with multiple injections of variably contaminated magma, whereas the surrounding part of the intrusion experienced a less vigorous emplacement history. No correlation is observed between the strontium and sulfur isotope compositions. This is explained by bulk assimilation of the silicate magma in a deeper staging magma chamber and variable assimilation of sulfur during magma transport into the Kevitsa magma chamber. The low level of metals in false ore and the Ni-depleted nature of its olivine suggest that some sulfides may have precipitated and deposited in the feeder conduit during the initial stage of magma emplacement. Cannibalization of early-formed sulfides by later magma injections may have been important in the formation of the economic ore deposit.

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

    USGS Publications Warehouse

    Gosselin, D.C.; Harvey, F.E.; Frost, C.; Stotler, R.; Macfarlane, P.A.

    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. ?? 2003 Elsevier Ltd. All rights reserved.

  18. Chromium Isotopes in Carbonates - a Tracer for Climate Change and for Reconstructing the Redox state of Ancient Seawater

    NASA Astrophysics Data System (ADS)

    Frei, R.; Gaucher, C.; Dossing, L. N.; Sial, A. N.

    2011-12-01

    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 climatic changes. We here present results of a new isotopic tracer system - stable chromium isotopes - applied to a late Ediacaran (Vendian) marine carbonate sequence exposed in the Calera de Recalde syncline, Arroyo del Soldado Group, Uruguay. The aim was to compare Cr isotope signatures directly to δ13C, 87Sr/86Sr and 143Nd/144Nd fluctuations in a well defined stratigraphic profile comprising sediments that were deposited during cold-warm periods accompanied by sea-level changes in response to glaciation-deglaciation at higher latitudes. The studied section is characterized by a pronounced negative (down to -3.3%) δ13C excursion in carbonates paralleled by a decrease of 87Sr/86Sr values. Chromium isotope signatures over this section also show a correlated decrease in δ53Cr (δ53Cr = [(53Cr/52Cr)sample/(53Cr/52Cr)SRM979)-1] x 1000) values from ~+0.29to -0.17% which mirrors a decrease in positively fractioned seawater signatures to slightly negative values characteristic of high-temperature magmatic sources. Linear correlations between δ53Cr and ɛNd(T=570 Ma), 87Sr/86Sr and Cr concentrations can be explained by mixing between two major input sources of Cr, Nd and Sr into the shallow seawater: 1) a source characterized by negative δ53Cr values of ~-0.2% , low 87Sr/86Sr values of ~0.707, and elevated 147Sm/144Nd values of ~0.13, recognized as a subaqueous hydrothermal dominated input source, and 2) a source characterized by positively fractionated δ53Cr values of ~+0.2%, higher 87Sr/86Sr values of ~0.708, and lower 147Sm/144Nd values of ~0.11, a source which is strongly affected by continentally derived input. Chromium isotopes provide a powerful tool for reconstructing

  19. Late Quaternary changes in desert dust inputs to the Red Sea and Gulf of Aden from 87Sr/ 86Sr ratios in deep-sea cores

    NASA Astrophysics Data System (ADS)

    Stein, Mordechai; Almogi-Labin, Ahuva; Goldstein, Steven L.; Hemleben, Christoph; Starinsky, Abraham

    2007-09-01

    Strontium isotope ratios of the HCL-insoluble residue ("ISR") and foraminifera of cores from the Red Sea and Gulf of Aden are used to monitor effects of hydrothermal, fluvial and desert dust transport to these regions during the past ˜ 0.5 Ma. While the Gulf of Aden was open-ocean, during low glacial sea levels the Red Sea was a semi-isolated basin, allowing the possibility to study the effects regional versus global inputs during glacial-interglacial cycles. The ISR from the Gulf of Aden and the Red Sea display different ranges of 87Sr/ 86Sr ratios of 0.7085-0.7107 and 0.7062-0.7085, respectively. These reflect mixtures between three components: granitic, hydrothermal and loess strontium with representative 87Sr/ 86Sr of ˜ 0.711; ˜ 0.706 and ˜ 0.7085, respectively. Gulf of Aden ISR represent mixtures of the loess and "granitic" sources, while Red Sea ISR are mixtures of the loess and sea floor "hydrothermal" sources. In the Gulf of Aden, loess sources dominate during glacials, indicating intensification of the NE moonsonal wind regime, and granitic sources dominate during interglacials, reflecting wetter conditions related to an enhanced regional SW monsoon. Red Sea ISR show no clear glacial-interglacial distinction, but display a general temporal increase in 87Sr/ 86Sr ratios over the past 380 ka toward loess-like values, indicating increasing loess contributions toward the present day. The ranges of ISR 87Sr/ 86Sr ratios in the Red Sea and the Gulf of Aden were distinct prior to the last glacial period (< 60 ka), when they converge at loess values. The increasing loess signal may be due to increasing aridity in the dust source regions, or increasing accumulation and availability of loess with progressive glacial cycles. Superimposed on the Red Sea general trend are shifts to higher 87Sr/ 86Sr ratios following major climate transitions (at ˜ 10, ˜ 80, ˜ 130, ˜ 190, ˜ 240 and ˜ 330 ka BP) that coincide with sapropel episodes in the Eastern Mediterranean

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

    NASA Astrophysics Data System (ADS)

    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.

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

    USGS Publications Warehouse

    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.

  2. Shifting material source of Chinese Loess since ~2.7 Ma reflected by Sr isotopic composition.

    PubMed

    Zhang, Wenfang; Chen, Jun; Li, Gaojun

    2015-05-21

    Deciphering the sources of eolian dust on the Chinese Loess Plateau (CLP) is fundamental to reconstruct paleo-wind patterns and paleo-environmental changes. Existing datasets show contradictory source evolutions of eolian dust on the CLP, both on orbital and tectonic timescales. Here, the silicate Sr and Nd isotopic compositions of a restricted grain size fraction (28-45 μm) were measured to trace the source evolution of the CLP since ~2.7 Ma. Our results revealed an unchanged source on orbital timescales but a gradual source shift from the Qilian Mountains to the Gobi Altay Mountains during the past 2.7 Ma. Both tectonic uplift and climate change may have played important roles for this shift. The later uplift of the Gobi Altay Mountains relative to the Qilian Mountains since 5 ± 3 Ma might be responsible for the increasing contribution of Gobi materials to the source deserts in Alxa arid lands. Enhanced winter monsoon may also facilitate transportation of Gobi materials from the Alxa arid lands to the CLP. The shifting source of Asian dust was also reflected in north Pacific sediments. The finding of this shifting source calls for caution when interpreting the long-term climate changes based on the source-sensitive proxies of the eolian deposits.

  3. Optimization Techniques for Improving the Precision of Isotopic Analysis by Thermal Ionization Mass Spectrometry

    NASA Astrophysics Data System (ADS)

    Wang, G. Q.; Xu, J. F.; Wu-Yang, S. Q.

    2016-12-01

    Operation of instruments and preparation of samples are also significant factors that can affect the precision of TIMS analyses, in addition to instrument hardware. We have reviewed the isotopic data of several standard materials at our TIMS lab for 5 years. It is suggested that several optimization techniques should be used in order to obtain high-precision isotopic ratio data: (1) It is important to choose a suitable filament material for isotopic measurements. We have established that W filament is likely the most efficient for ionizing Sr when selecting from W, Re, and Ta; meanwhile, Re filament can produce a higher intensity for Nd isotopes than W and Ta filament can. It is concluded that the best TIMS signals are obtained for Sr using W signal-filaments and for Nd using Re double-filaments. (2) The preparation of the activator plays a key role in the analysis of some isotopic ratios. This study indicates that choosing a suitable activator can greatly elevate the precision of 206Pb/204Pb ratios during Pb isotopic measurements. We have suggested a new scheme to make an activator by using a mixture of 10% Si-gel + 7.5% H3PO3 + 82.5% H2O (weight %). (3) It is necessary to re-set the cup configuration to avoid cup degradation when operating for a long period of time (a year or more). We propose a new cup configuration to avoid this disadvantage during Sr isotopic analyses. (4) The contamination of 187Re and 185Re after using Re-filament could be eliminated by cleaning the ion source and baking the source housing.

  4. Late Quaternary Productivity Records from Coccolith Sr/Ca

    NASA Astrophysics Data System (ADS)

    Stoll, H. M.; Burke, A.; Mejia Ramirez, L. M.; Shimizu, N.; Ziveri, P. P. I.

    2014-12-01

    The Sr/Ca of coccoliths has been proposed as an indicator of productivity on the basis of correlation with export production in sediment traps and across upwelling productivity gradients, although the mechanism responsable for this relationship is not clear. For diverse oceanographic settings in the Late Quaternary, we compare coccolith Sr/Ca productivity records with those of other productivity indicators and proxies for mechanisms of productivity forcing. For the Somalia Basin in the Arabian Sea, coccolith Sr/Ca shows a large variation coherent with precessional forcing of wind strength as a mechanism for productivity regulation. During the glacial, the Sr/Ca peak is decoupled from productivity indicators based on organic C accumulation rate. For the Northern Bay of Bengal, coccolith Sr/Ca, Ba/Ti, and relative abundance of G. bulloides, all suggest greater productivity during the interglacial periods, consisted with Nd isotopic evidence for greater riverine nutrient inputs. In the Andaman Sea, coccolith Sr/Ca is highest during precessional maxima in the summer monsoon, consistent with proxies for chemical weathering in the Irawaddy rivershed. In the Eastern Mediterranean, coccolith Sr/Ca is on average low, and peaks during the E. Holocene interval characterized by deposition of sapropel S1. The peak in Sr/Ca however is comparable to the level maintained throughout the Holocene in the Western Mediterranean, where no sapropel occurs, implicating deepwater oxygen levels as a significant contributor to sapropel formation. Finally, on the Agulhas Bank, minima in coccolith Sr/Ca occur during obliquity minima which are periods of anomalous equatorward deposition of IRD in the Southern Ocean. Northward explansion of the westerly wind field during these cold intervals, block upwelling on the Agulhas Bank and result in low productivity.

  5. Precise determination of δ88Sr in rocks, minerals, and waters by double-spike TIMS: A powerful tool in the study of chemical, geologic, hydrologic and biologic processes

    USGS Publications Warehouse

    Neymark, Leonid A.; Premo, Wayne R.; Mel'nikov, Nikolay N.; Emsbo, Poul

    2014-01-01

    We present strontium isotopic (88Sr/86Sr and 87Sr/86Sr) results obtained by 87Sr–84Sr double spike thermal ionization mass-spectrometry (DS-TIMS) for several standards as well as natural water samples and mineral samples of abiogenic and biogenic origin. The detailed data reduction algorithm and a user-friendly Sr-specific stand-alone computer program used for the spike calibration and the data reduction are also presented. Accuracy and precision of our δ88Sr measurements, calculated as permil (‰) deviations from the NIST SRM-987 standard, were evaluated by analyzing the NASS-6 seawater standard, which yielded δ88Sr = 0.378 ± 0.009‰. The first DS-TIMS data for the NIST SRM-607 potassium feldspar standard and for several US Geological Survey carbonate, phosphate, and silicate standards (EN-1, MAPS-4, MAPS-5, G-3, BCR-2, and BHVO-2) are also reported. Data obtained during this work for Sr-bearing solids and natural waters show a range of δ88Sr values of about 2.4‰, the widest observed so far in terrestrial materials. This range is easily resolvable analytically because the demonstrated external error (±SD, standard deviation) for measured δ88Sr values is typically ≤0.02‰. It is shown that the “true” 87Sr/86Sr value obtained by the DS-TIMS or any other external normalization method combines radiogenic and mass-dependent mass-fractionation effects, which cannot be separated. Therefore, the “true” 87Sr/86Sr and the δ87Sr parameter derived from it are not useful isotope tracers. Data presented in this paper for a wide range of naturally occurring sample types demonstrate the potential of the δ88Sr isotope tracer in combination with the traditional radiogenic 87Sr/86Sr tracer for studying a variety of biological, hydrological, and geological processes.

  6. Tellurium Stable Isotope Fractionation in Chondritic Meteorites

    NASA Astrophysics Data System (ADS)

    Fehr, M. A.; Hammond, S. J.; Parkinson, I. J.

    2014-09-01

    New Te double spike procedures were set up to obtain high-precision accurate Te stable isotope data. Tellurium stable isotope data for 16 chondrite falls are presented, providing evidence for significant Te stable isotope fractionation.

  7. A Fifty-Year Coral Sr/Ca Time Series from Guam, Mariana Islands: In situ Monitoring and Comparison to Observed Pacific Climate

    NASA Astrophysics Data System (ADS)

    Lander, M.

    2016-12-01

    Located on the northern edge of the West Pacific Warm Pool, Guam is positioned to obtain uniquely valuable natural records of west Pacific maritime paleoclimate. This study is the first to evaluate the application of the coral Sr/Ca sea surface temperature (SST) proxy to the reconstruction of Guam's climate history. To help test the fidelity of the coral Sr/Ca proxy to actual climate, and how it might be affected by environmental variables—on Guam or elsewhere—the study documented monthly seawater oxygen isotope ratios (δ18O), pH, cation, and nitrate concentrations from September 2009 to December 2010 at a Porites lutea colony in Guam's Apra Harbor. The study site was chosen for its accessibility, so that environmental conditions could be readily monitored. A 50-year Sr/Ca record was carefully compared to instrumental records, the quality and reliability of which were also closely examined. Time series of seawater δ18O, pH, and cation concentrations show some evidence of freshwater input from direct rainfall or stream discharge into the harbor. The Sr/Ca proxy SST results, however, are robust, and do not appear to have been significantly affected. The Sr/Ca proxy reproduces the long-term warming trend observed in the historical records of regional SST and local air temperature. Moreover, it shows remarkable fidelity to regional ocean-atmosphere variations as represented by the indices of the El Niño/Southern Oscillation and the Pacific Decadal Oscillation. The consistency of the results with Guam's historical instrumental records, with previous δ18O results from Guam, and with previous Sr/Ca proxy results in similar environments elsewhere, demonstrate the efficacy of accessible near-shore sites for obtaining reliable Sr/Ca climate proxies, and the utility of Guam as a source for accurate coral records of western Pacific Ocean regional climate.

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

    NASA Astrophysics Data System (ADS)

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

    2016-03-01

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

  9. Using stable isotopes of water and strontium to investigate the hydrology of a natural and a constructed wetland

    USGS Publications Warehouse

    Hunt, R.J.; Bullen, T.D.; Krabbenhoft, D.P.; Kendall, C.

    1998-01-01

    Wetlands cannot exist without water, but wetland hydrology is difficult to characterize. As a result, compensatory wetland mitigation often only assumes the proper hydrology has been created. In this study, water sources and mass transfer processes in a natural and constructed wetland complex were investigated using isotopes of water and strontium. Water isotope profiles in the saturated zone revealed that the natural wetland and one site in the constructed wetland were primarily fed by ground water; profiles in another constructed wetland site showed recent rain was the predominant source of water in the root zone. Water isotopes in the capillary fringe indicated that the residence time for rain is less in the natural wetland than in the constructed wetland, thus transpiration (an important water sink) was greater in the natural wetland. Strontium isotopes showed a systematic difference between the natural and constructed wetlands that we attribute to the presence or absence of peat. In the peat-rich natural wetland, ??87Sr in the pore water increased along the flowline due to preferential weathering of minerals containing radiogenic Sr in response to elevated Fe concentrations in the water. In the constructed wetland, where peat thickness was thin and Fe concentrations in water were negligible, ??87Sr did not increase along the flowline. The source of the peat (on-site or off-site derived) applied in the constructed wetland controlled the ??87Sr at the top of the profile, but the effects were restricted by strong cation exchange in the underlying fluvial sediments. Based on the results of this study, neither constructed wetland site duplicated the water source and weathering environment of the adjoining natural wetland. Moreover, stable isotopes were shown to be effective tools for investigating wetlands and gaining insight not easily obtained using non-isotopic techniques. These tools have potential widespread application to wetlands that have distinct isotopic

  10. Mafic dykes intrusive into Pre-Cambrian rocks of the São Luís cratonic fragment and Gurupi Belt (Parnaíba Province), north-northeastern Brazil: Geochemistry, Sr-Nd-Pb-O isotopes, 40Ar/39Ar geochronology, and relationships to CAMP magmatism

    NASA Astrophysics Data System (ADS)

    Klein, Evandro L.; Angélica, Rômulo S.; Harris, Chris; Jourdan, Fred; Babinski, Marly

    2013-07-01

    Dykes of diabase and microgabbro intruded into Pre-Cambrian rocks of the São Luís cratonic fragment and Gurupi Belt, which are tectonic and erosive windows of the Parnaíba Basin in north-northeastern Brazil. Ar-Ar ages were determined, and major, trace element, and Nd-Sr-Pb-O isotopic compositions of these dykes were measured to provide insights into their age, and into the nature of their mantle sources and petrogenetic processes. The data have also been used to compare the chemical and isotopic signatures of the dykes with those of the Central Atlantic Magmatic Province (CAMP). Four chemical groups of mafic dykes have been identified. These comprise two subtypes of high-Ti rocks (i) HTi-1 (TiO2 < 2.3 wt.%; SiO2 > 47 wt.%), (ii) HTi-2 (TiO2 > 2.7 wt.%; SiO2 > 47 wt.%), in addition to (iii) evolved high-Ti (TiO2 > 4 wt.%; SiO2 of ~ 46 wt.%) and (iv) low-Si (TiO2 > 2.2 wt.%; SiO2 < 45 wt.%) rocks. 40Ar/39Ar geochronology of plagioclase returned ages of 201 ± 4 Ma and 193 ± 10 Ma for the HTi-2 subtype, and of 201 ± 2 Ma and 207 ± 9 Ma for the evolved high-Ti group. The HTi-1 and low-Si groups presented highly disturbed age spectra, and did not allow the definition of their emplacement ages. The Argon data indicate an age > 200 Ma for the low-Si group and are dubious with respect to the age of theHTi-1 subtype, if coeval with (i.e., ~ 200 Ma), or older than, the HTi-2 and evolved high-Ti types. All groups present δ18O values of pyroxene that are compatible with uncontaminated mantle-derived magmas. The HTi-1 subtype (average 143Nd/144Nd200 = 0.512644; 87Sr/86Sr200 = 0.7035; 206Pb/204Pb of 17.86) shows the less enriched and less fractionated (more primitive) trace element distribution of all groups. The HTi-2 subtype shows enriched trace element pattern and depleted Nd-Sr signature (143Nd/144Nd200 = 0.512610; 87Sr/86Sr200 = 0.7037) and average 206Pb/204Pb ratios of 17.23. The evolved high-Ti chemical group shows average ratios of 143Nd/144Nd200 = 0.512558, 87Sr

  11. Calcium and strontium isotope fractionation during precipitation from aqueous solutions as a function of temperature and reaction rate; II. Aragonite

    NASA Astrophysics Data System (ADS)

    AlKhatib, Mahmoud; Eisenhauer, Anton

    2017-07-01

    In order to study Strontium (Sr) partitioning and isotope fractionation of Sr and Calcium (Ca) in aragonite we performed precipitation experiments decoupling temperature and precipitation rates (R∗, μmol/m2 h) in the interval of about 2.3-4.5 μmol/m2 h. Aragonite is the only pure solid phase precipitated from a stirred solutions exposed to an atmosphere of NH3 and CO2 gases throughout the spontaneous decomposition of (NH4)2CO3. The order of reaction with respect to Ca ions is one and independent of temperature. However, the order of reaction with respect to the dissolved inorganic carbon (DIC) is temperature dependent and decreases from three via two to one as temperature increases from 12.5 and 25.0 to 37.5 °C, respectively. Strontium distribution coefficient (DSr) increases with decreasing temperature. However, R∗ responds differently depending on the initial Sr/Ca concentration and temperature: at 37.5 °C DSr increase as a function of increasing R∗ but decrease for 12.5 and 25 °C. Not seen at 12.5 and 37.5 °C but at 25 °C the DSr-R∗ gradient is also changing sign depending on the initial Sr/Ca ratio. Magnesium (Mg) adsorption coefficient between aragonite and aqueous solution (DMg) decreases with temperature but increases with R∗ in the range of 2.4-3.8 μmol/m2 h. Strontium isotope fractionation (Δ88/86Sraragonite-aq) follows the kinetic type of fractionation and become increasingly negative as a function of R∗ for all temperatures. In contrast Ca isotope fractionation (Δ44/40Caaragonite-aq) shows a different behavior than the Sr isotopes. At low temperatures (12.5 and 25 °C) Ca isotope fractionation (Δ44/40Caaragonite-aq) becomes positive as a function of R∗. In contrast, at 37.5 °C and as a function of increasing R∗ the Δ44/40Caaragonite-aq show a Sr type like behavior and becomes increasingly negative. Concerning both the discrepant behavior of DSr as a function of temperature as well as for the Ca isotope fractionation as a

  12. Impacts of Dust on Tropical Volcanic Soil Formation: Insights from Strontium and Uranium-Series Isotopes in Soils from Basse-Terre Island, French Guadeloupe

    NASA Astrophysics Data System (ADS)

    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

  13. Origin discrimination of defatted pork via trace elements profiling, stable isotope ratios analysis, and multivariate statistical techniques.

    PubMed

    Park, Yu Min; Lee, Cheong Mi; Hong, Joon Ho; Jamila, Nargis; Khan, Naeem; Jung, Jong-Hyun; Jung, Young-Chul; Kim, Kyong Su

    2018-09-01

    This study verified the origin of 346 defatted Korean and non-Korean pork samples via trace elements profiling, and C and N stable isotope ratios analysis. The analyzed elements were 6 Li, 7 Li, 10 B, 11 B, 51 V , 50 Cr, 52 Cr, 53 Cr, 55 Mn, 58 Ni, 60 Ni, 59 Co, 63 Cu, 65 Cu, 64 Zn, 66 Zn, 69 Ga, 71 Ga, 75 As, 82 Se, 84 Sr, 86 Sr, 87 Sr, 88 Sr, 85 Rb, 94 Mo, 95 Mo, 97 Mo, 107 Ag, 109 Ag, 110 Cd, 111 Cd, 113 Cd, 112 Cd, 114 Cd, 116 Cd, 133 Cs, 206 Pb, 207 Pb, and 208 Pb. Content (mg/kg) of 51 V (0.012), 50 Cr (0.882), 75 As (0.017), 85 Rb (57.7), and 87 Sr (46.3) were high in Korean pork samples whereas 6 Li, 7 Li, 59 Co, 55 Mn, 58 Ni, 84 Sr, 86 Sr, 88 Sr, 111 Cd, and 133 Cs were found higher in non-Korean samples. The results of discriminant analysis showed that the trace elements content and stable isotope ratios were significant for the discrimination of geographical origins with a perfect discrimination rate of 100%. Copyright © 2018 Elsevier Ltd. All rights reserved.

  14. Rare earth abundances and Rb-Sr systematics of basalts, gabbro, anorthosite and minor granitic rocks from the Indian Ocean Ridge System, Western Indian Ocean

    USGS Publications Warehouse

    Hedge, C.E.; Futa, K.; Engel, C.G.; Fisher, R.L.

    1979-01-01

    Basalts dredged from the Mid-Indian Ocean Ridge System have rare earth, Rb, and Sr concentrations like those from other mid-ocean ridges, but have slightly higher Sr87/Sr86 ratios. Underlying gabbroic complexes are similar to the basalts in Sr87/Sr86, but are poorer K, Rb, and in rare earths. The chemical and isotopic data, as well as the geologic relations suggest a cumulate origin for the bulk of the gabbroic complexes. ?? 1979 Springer-Verlag.

  15. Petrology and isotopic geochemistry of the Archaean basement lithologies near Gardiner, Montana

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Guy, R.E.; Sinha, A.K.

    1985-01-01

    In an attempt to recognize potential source rocks for some of the rhyolites of the Yellowstone Rhyolite Plateau, four major exposures of Precambrian rocks have been analyzed for major and trace elements and isotopic composition. The terrain is characterized by granitic gneisses with subordinant mica schist, quartzite, amphibolite, and two-mica granite. The gneiss units from the northern (Yankee Jim Canyon) and eastern (Lamar Canyon) outcrops are characterized by k-feldspar augen in a gneissic groundmass of two-feldspar--quartz--mica--epidote. The feldspar compositions are Or/sub 95/ and An/sub 5-15/ indicating metamorphic re-equilibration. Mafic phases are iron-rich with Fe:Mg of 1.0 in epidote, 0.7 inmore » pyroxene, and 0.5 in biotite. Sr isotopic analyses yield present day values of 0.7201-0.7519 for Lamar Canyon, 0.7157-0.7385 for Yankee Jam Canyon, and 0.7200-0.7679 for mica schist from the western and northern outcrops. Rb-Sr whole-rock data indicate a complicated isotopic history with ages ranging from 2800 to 3600 my. The 2800 my ages are consistent with ages for the Tobacco Root and Ruby Mountains to the NW (James and Hedge, 1980) and the Beartooth Range to the NE (Nunes and Tilton, 1971) while the 3600 my age may be related to the formation of the protolith. The rhyolites of the northern Yellowstone Rhyolite Plateau (Sr/sub I/=0.7100) cannot be derived from the exposed Archaean rocks based on Sr isotopic and whole-rock chemistry, and must be derived from lithologies not exposed in the area. This study shows that care must be taken when using surface lithologies to model potential sources materials for volcanic rocks in an associated terrain.« less

  16. Trace elements and isotope data of the Um Garayat gold deposit, Wadi Allaqi district, Egypt

    NASA Astrophysics Data System (ADS)

    Zoheir, Basem; Emam, Ashraf; Pitcairn, Iain K.; Boskabadi, Arman; Lehaye, Yann; Cooper, Matthew J.

    2018-04-01

    Trace element composition of sulfides and O, C, Sr and S isotopic data are assessed to constrain the evolution and potential fluid and metal sources of the Um Garayat gold deposit. Ore microscopy and BSE investigations of quartz veins show blocky arsenopyrite and pyrite replaced in part by pyrrhotite, chalcopyrite, sphalerite, galena, and gersdorffite. Free-milling gold occurs commonly in close association with the late sulfides, and along fractures in pyrite. On the other hand, recrystallized pyrite is disseminated in host metavolcaniclastic/metasedimentary rocks that commonly contain carbonaceous material. In situ LA-ICP-MS analysis of sulfides shows the recrystallized pyrite enriched in most trace elements, while blocky pyrite contains only some traces of arsenic. Detected concentrations of gold (up to 17 ppm) were only reported in arsenopyrite disseminated in quartz veins. The δ34S values of blocky pyrite and pyrrhotite in quartz veins define a narrow range (1.6 to 3.7‰), suggesting a homogenous sulfur source which is consistent with the dominantly mafic host rocks. The recrystallized pyrite has a distinctive sulfur isotope composition (δ34S - 9.3 to - 10.6‰), which is rather comparable to diagenetic sulfides. Hydrothermal carbonate in quartz veins and wallrock have nearly constant values of δ18O (10.5 to 11.9‰) and δ13C (- 4.2 to - 5.5‰). Based on constraints from mineral assemblages and chlorite thermometry, data of six samples indicate that carbonate precipitation occurred at 280 °C from a homogenous hydrothermal fluid with δ18OH2O 4.4 ± 0.7‰ and δ13C = 3.7 ± 0.8‰. Strontium isotope values of two samples (87Sr/86Sr = 0.7024 and 0.7025) are similar to the initial 87Sr/86Sr ratios of island arc metabasalts ( 710 Ma) in the South Eastern Desert. The generally homogenous sulfur, C, O, Sr isotope data are suggestive of metamorphogenic fluids, likely produced from dominantly mafic volcanic rocks at the greenschist-amphibolite facies transition.

  17. Tracing the Geographical Origin of Onions by Strontium Isotope Ratio and Strontium Content.

    PubMed

    Hiraoka, Hisaaki; Morita, Sakie; Izawa, Atsunobu; Aoyama, Keisuke; Shin, Ki-Cheol; Nakano, Takanori

    2016-01-01

    The strontium (Sr) isotope ratio ((87)Sr/(86)Sr) and Sr content were used to trace the geographical origin of onions from Japan and other countries, including China, the United States of America, New Zealand, Australia, and Thailand. The mean (87)Sr/(86)Sr ratio and Sr content (dry weight basis) for onions from Japan were 0.70751 and 4.6 mg kg(-1), respectively, and the values for onions from the other countries were 0.71199 and 12.4 mg kg(-1), respectively. Linear discriminant analysis was performed to classify onions produced in Japan from those produced in the other countries based on the Sr data. The discriminant equation derived from linear discriminant analysis was evaluated by 10-fold cross validation. As a result, the origins of 92% of onions were correctly classified between Japan and the other countries.

  18. Constraining seasonal active layer dynamics and chemical weathering reactions occurring in North Slope Alaskan watersheds with major ion and isotope (δ34SSO4, δ13CDIC, 87Sr/86Sr, δ44/40Ca, and δ44/42Ca) measurements

    NASA Astrophysics Data System (ADS)

    Lehn, Gregory O.; Jacobson, A. D.; Douglas, T. A.; McClelland, J. W.; Barker, A. J.; Khosh, M. S.

    2017-11-01

    Rising air temperatures in the Arctic may destabilize a large pool of organic carbon stored in permafrost, thereby causing a positive feedback to global climate warming. Permafrost thaw could also deepen hydrologic flow paths and expose previously frozen rock and mineral fragments to chemical weathering. Future shifts in the inorganic solute geochemistry of Arctic rivers may signal changes in soil processes that also affect organic carbon storage. Tracing permafrost thaw with dissolved riverine loads requires understanding the spatial and seasonal variation of chemical weathering reactions and other biogeochemical phenomena that affect elemental mass-transport. To help identify connections between mineral weathering and active layer processes, we studied the major ion and isotope (δ34SSO4, δ13CDIC, 87Sr/86Sr, δ44/40Ca, and δ44/42Ca) geochemistry of five streams draining the North Slope of Alaska. Continuous permafrost underlies all streams, but the Atigun River, Roche Moutonnée Creek, and Trevor Creek primarily drain bare bedrock outcrops in the Brooks Range, while the Upper Kuparuk River and Imnavait Creek primarily drain tundra. In total, we collected 546 water samples spanning the spring freshet through fall freeze-up in 2009 and 2010. We also analyzed snow, rock, sediment, soil, and plant samples. Major ion ratios and δ13CDIC values point to the overall dominance of carbonate weathering by carbonic and sulfuric acids, with additional influences from atmospheric deposition, plant decay, sulfate salt dissolution, and silicate weathering by carbonic acid. δ13CDIC values may also reflect partial equilibration with soil and atmospheric CO2. All streams display large seasonal variations in major ion ratios and δ13CDIC values that are consistent with progressive deepening of the seasonally thawed zone over the summer. In the mountain watersheds, carbonate weathering dominates during the spring and summer, while sulfate salt (primarily CaSO4 and MgSO4

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

    USGS Publications Warehouse

    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.

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

    NASA Astrophysics Data System (ADS)

    Paces, James B.; Wurster, Frederic C.

    2014-09-01

    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.

  1. Mineral dissolution in the Cape Cod aquifer, Massachusetts, USA: I . Reaction stoichiometry and impact of accessory feldspar and glauconite on strontium isotopes, solute concentrations, and REY distribution

    USGS Publications Warehouse

    Bau, Michael; Alexander, Brian; Chesley, John T.; Dulski, Peter; Brantley, Susan L.

    2004-01-01

    To compare relative reaction rates of mineral dissolution in a mineralogically simple groundwater aquifer, we studied the controls on solute concentrations, Sr isotopes, and rare earth element and yttrium (REY) systematics in the Cape Cod aquifer. This aquifer comprises mostly carbonate-free Pleistocene sediments that are about 90% quartz with minor K-feldspar, plagioclase, glauconite, and Fe-oxides. Silica concentrations and pH in the groundwater increase systematically with increasing depth, while Sr isotopic ratios decrease. No clear relationship between 87Sr/86Sr and Sr concentration is observed. At all depths, the 87Sr/86Sr ratio of the groundwater is considerably lower than the Sr isotopic ratio of the bulk sediment or its K-feldspar component, but similar to that of a plagioclase-rich accessory separate obtained from the sediment. The Si-87Sr/86Sr-depth relationships are consistent with dissolution of accessory plagioclase. In addition, solutes such as Sr, Ca, and particularly K show concentration spikes superimposed on their respective general trends. The K-Sr-87Sr/86Sr systematics suggests that accessory glauconite is another major solute source to Cape Cod groundwater. Although the authigenic glauconite in the Cape Cod sediment is rich in Rb, it is low in in-grown radiogenic 87Sr because of its young Pleistocene age. The low 87Sr/86Sr ratios are consistent with equilibration of glauconite with seawater. The impact of glauconite is inferred to vary due to its variable abundance in the sediments. In the Cape Cod groundwater, the variation of REY concentrations with sampling depth resembles that of K and Rb, but differs from that of Ca and Sr. Shale-normalized REY patterns are light REY depleted, show negative Ce anomalies and super-chondritic Y/Ho ratios, but no Eu anomalies. REY input from feldspar, therefore, is insignificant compared to input from a K-Rb-bearing phase, inferred to be glauconite. These results emphasize that interpretation of groundwater

  2. Thermal effects on rare earth element and strontium isotope chemistry in single conodont elements

    NASA Astrophysics Data System (ADS)

    Armstrong, H. A.; Pearson, D. G.; Griselin, M.

    2001-02-01

    A low-blank, high sensitivity isotope dilution, ICP-MS analytical technique has been used to obtain REE abundance data from single conodont elements weighing as little as 5 μg. Sr isotopes can also be measured from the column eluants enabling Sr isotope ratios and REE abundance to be determined from the same dissolution. Results are comparable to published analyses comprising tens to hundreds of elements. To study the effects of thermal metamorphism on REE and strontium mobility in conodonts, samples were selected from a single bed adjacent to a basaltic dyke and from the internationally used colour alteration index (CAI) "standard set." Our analyses span the range of CAI 1 to 8. Homogeneous REE patterns, "bell-shaped" shale-normalised REE patterns are observed across the range of CAI 1 to 6 in both sample sets. This pattern is interpreted as the result of adsorption during early diagenesis and could reflect original seawater chemistry. Above CAI 6 REE patterns become less predictable and perturbations from the typical REE pattern are likely to be due to the onset of apatite recrystallisation. Samples outside the contact aureole of the dyke have a mean 87Sr/ 86Sr ratio of 0.708165, within the broad range of published mid-Carboniferous seawater values. Our analysis indicates conodonts up to CAI 6 record primary geochemical signals that may be a proxy for ancient seawater.

  3. Fingerprints for main varieties of argentinean wines: terroir differentiation by inorganic, organic, and stable isotopic analyses coupled to chemometrics.

    PubMed

    Di Paola-Naranjo, Romina D; Baroni, Maria V; Podio, Natalia S; Rubinstein, Hector R; Fabani, Maria P; Badini, Raul G; Inga, Marcela; Ostera, Hector A; Cagnoni, Mariana; Gallegos, Ernesto; Gautier, Eduardo; Peral-Garcia, Pilar; Hoogewerff, Jurian; Wunderlin, Daniel A

    2011-07-27

    Our main goal was to investigate if robust chemical fingerprints could be developed for three Argentinean red wines based on organic, inorganic, and isotopic patterns, in relation to the regional soil composition. Soils and wines from three regions (Mendoza, San Juan, and Córdoba) and three varieties (Cabernet Sauvignon, Malbec, and Syrah) were collected. The phenolic profile was determined by HPLC-MS/MS and multielemental composition by ICP-MS; (87)Sr/(86)Sr and δ(13)C were determined by TIMS and IRMS, respectively. Chemometrics allowed robust differentiation between regions, wine varieties, and the same variety from different regions. Among phenolic compounds, resveratrol concentration was the most useful marker for wine differentiation, whereas Mg, K/Rb, Ca/Sr, and (87)Sr/(86)Sr were the main inorganic and isotopic parameters selected. Generalized Procrustes analysis (GPA) using two studied matrices (wine and soil) shows consensus between them and clear differences between studied areas. Finally, we applied a canonical correlation analysis, demonstrating significant correlation (r = 0.99; p < 0.001) between soil and wine composition. To our knowledge this is the first report combining independent variables, constructing a fingerprint including elemental composition, isotopic, and polyphenol patterns to differentiate wines, matching part of this fingerprint with the soil provenance.

  4. Joint profiling of greenhouse gases, isotopes, thermodynamic variables, and wind from space by combined microwave and IR laser occultation: the ACCURATE concept

    NASA Astrophysics Data System (ADS)

    Kirchengast, G.; Schweitzer, S.

    2008-12-01

    The ACCURATE (Atmospheric Climate and Chemistry in the UTLS Region And climate Trends Explorer) mission was conceived at the Wegener Center in late 2004 and subsequently proposed in 2005 by an international team of more than 20 scientific partners from more than 12 countries to an ESA selection process for next Earth Explorer Missions. While the mission was not selected for formal pre-phase A study, it received very positive evaluation and was recommended for further development and demonstration. ACCURATE employs the occultation measurement principle, known for its unique combination of high vertical resolution, accuracy and long-term stability, in a novel way. It systematically combines use of highly stable signals in the MW 17-23/178-196 GHz bands (LEO-LEO MW crosslink occultation) with laser signals in the SWIR 2-2.5 μm band (LEO-LEO IR laser crosslink occultation) for exploring and monitoring climate and chemistry in the atmosphere with focus on the UTLS region (upper troposphere/lower stratosphere, 5-35 km). The MW occultation is an advanced and at the same time compact version of the LEO-LEO MW occultation concept, studied in 2002-2004 for the ACE+ mission project of ESA for frequencies including the 17-23 GHz band, complemented by U.S. study heritage for frequencies including the 178-196 GHz bands (R. Kursinski et al., Univ. of Arizona, Tucson). The core of ACCURATE is tight synergy of the IR laser crosslinks with the MW crosslinks. The observed parameters, obtained simultaneously and in a self-calibrated manner based on Doppler shift and differential log-transmission profiles, comprise the fundamental thermodynamic variables of the atmosphere (temperature, pressure/geopotential height, humidity) retrieved from the MW bands, complemented by line-of-sight wind, six greenhouse gases (GHGs) and key species of UTLS chemistry (H2O, CO2, CH4, N2O, O3, CO) and four CO2 and H2O isotopes (HDO, H218O, 13CO2, C18OO) from the SWIR band. Furthermore, profiles of

  5. Stratigraphic implications of trace element and strontium-isotope analyses of Kimmeridgian shell calcite from the Lower Saxony Basin, Germany

    NASA Astrophysics Data System (ADS)

    Zuo, Fanfan; Heimhofer, Ulrich; Huck, Stefan; Erbacher, Jochen; Bodin, Stephane

    2017-04-01

    Stratigraphic uncertainties due to the lack of open marine marker fossils (e.g. ammonites) hamper the precise age assignment and stratigraphic correlation of Kimmeridgian strata found in the Lower Saxony Basin of Northern Germany. Correlation of these deposits with the Jurassic standard ammonite zonation is still difficult, since the existing ostracod biostratigraphy is facies-controlled and of only limited stratigraphic precision. In this study, a chemostratigraphic approach has been chosen and biogenic shell material produced by brachiopods, oysters and lithiotids is evaluated for its reliability to act as proxy of the original Jurassic seawater strontium isotope composition. Low-Mg calcite shells have been collected from three stratigraphic sections accessible in open-cast quarries located in the Lower Saxony Basin of Northern Germany. In order to identify diagenetically altered shell calcite, trace element and stable isotope analysis of 227 calcite samples (oysters=101; brachiopods=60; Trichites=52) has been carried out. The geochemical results reveal that (1) concentration of different trace elements varies between the different groups of shell-forming organisms, which may be related to vital effects and (2) high strontium contents, low Mn and Fe contents and the lack of correlation between these elements indicate near-pristine calcite shells, and therefore shells are supposed to record the ambient sea water composition during the Late Jurassic. Strontium-isotope (87Sr/86Sr) analysis of diagenetically screened samples indicates an Early Kimmeridgian age of the studied deposits, which is in accordance with ostracod biostratigraphic data. An increasing trend in 87Sr/86Sr with stratigraphic height fits well with the global strontium-isotope curve. Besides, similar 87Sr/86Sr ratios derived from different organisms from a single stratigraphic level highlight the suitability of the shells for strontium-isotope stratigraphy. Despite the shallow-marine character of

  6. Chemical and isotopic fingerprinting of small ungauged watershed: How far the hydrological functioning can be understood?

    NASA Astrophysics Data System (ADS)

    Petelet-Giraud, Emmanuelle; Luck, Jean-Marc; Ben Othman, Dalila; Joseph, Christian; Négrel, Philippe

    2016-05-01

    This study presents the ability of major/trace elements together with strontium isotopes to trace water origins at small scale at the outlet of a small watershed (Peyne, Hérault, France). Two small sub-basins draining distinct lithologies in their headwater (Plio-Villafranchian conglomerate versus Triassic gypsum-rich marls and dolomites) and the Miocene formations downstream are investigated. The Ca/Na vs. Mg/Na ratios and Ca/Sr vs. 87Sr/86Sr ratios allow the different facies that imprint the water signature to be identified, according to the hydrological conditions (low/high flows). Moreover, Sr isotopes evidence the two distinct Miocene facies, the sandy marls and the marine carbonates. The variation of the signature at the outlet of the basin allows identifying the main contributing compartments according to the hydrological conditions. This approach, based on a limited number of samples, highlights the potential of geochemical and isotopic tracers to define the contributing compartments to the runoff at the outlet of a basin. It thus could be considered as a potential alternative way to classical hydrological monitoring to delineate the main contributing areas during floods, especially in small ungauged river basins, where most of the devastating flash floods are recorded.

  7. Strontium Isotopes of Gaskiers Cap Carbonate, Avalon, Newfoundland: Sequential Digestion Aids Interpretation of Petrologic Complexity

    NASA Astrophysics Data System (ADS)

    Tang, T.; Raub, T. D.; Wang, Z.

    2013-12-01

    Strontium isotope chemostratigraphy in limestones appear to track a near monotonic rising trend from the tail of the breakup of the supercontinent Rodinia at ~750 Ma into the latest Ediacaran Period at ~ 550 Ma (Halverson et al., 2007). This offers a potentially powerful tool to date carbonates occurring within this time period of stepwise environmental oxidation. Furthermore, aspects of the Snowball Earth hypothesis predict that some magnitude of 87Sr/86Sr excursions of seawater is expected at multiple intervals during this time, because balancing influences from prolonged synglacial hydrothermal input in entombed oceans, deglacial freshwater plumes of varying temperature and salinity, and enhanced postglacial silicate weathering from the continents can leave multiple isotopic trends plausible during these critical intervals. The positions of these deglaciations appear to correlate specifically to marine oxidation events, with cause/effect relations still under investigation. To capitalize on all of these interpretive possibilities, it is crucial to establish a high-precision and high-resolution strontium chemostratigraphic record over both short and long timescales. However, difficulties in establishing such a record based on carbonates are associated with 1) diagenetic influence over extensive geological time; and 2) petrologic complexities of the studied samples. Using a sequential digestion technique, Liu et al. (2013) demonstrated that these hurdles can be overcome, and that primary 87Sr/86Sr ratios of contemporaneous seawater can be obtained from Marinoan cap dolostones (~635 Ma), which have considerably less Sr than limestones, and whose Sr isotope compositions are commonly ignored in the strontium chemostratigraphic record. This leads to several viable, specific interpretations about the origin of Marinoan cap carbonate: either 1) very fast deposition; 2) slow deposition in a long-Sr-residence-time ocean; 3) mid-cap deposition in a freshwater "Glacial Lake

  8. RESEARCH NOTE: Slow-ridge/hotspot interactions from global gravity, seismic tomography and 87Sr/86Sr isotope data

    NASA Astrophysics Data System (ADS)

    Goslin, Jean; Thirot, Jean-Louis; Noël, Olivier; Francheteau, Jean

    1998-11-01

    Among the mantle hotspots present under oceanic areas, a large number are located on-or close to-active oceanic ridges. This is especially true in the slow-spreading Atlantic and Indian oceans. The recent availability of worldwide gravity grids and the increasing coverage of geochemical data sets along active spreading centres allow a fruitful comparison of these data with global geoid and seismic tomography models, and allow one to study interactions between mantle plumes and active slow-spreading ridges. The observed correlations allow us to draw preliminary conclusions on the general links between surficial processes, which shape the detailed morphology of the ridge axes, and deeper processes, active in the upper mantle below the ridge axial domains as a whole. The interactions are first studied at the scale of the Atlantic (the Mid-Atlantic Ridge from Iceland to Bouvet Island) from the correlation between the zero-age free-air gravity anomaly, which reflects the zero-age depth of the ridge axis, and Sr isotopic ratios of ridge axis basalts. The study is then extended to a more global scale (the slow ridges from Iceland to the Gulf of Aden) by including geoid and upper-mantle tomography models. The interactions appear complex, ranging from the effect of large and very productive plumes, almost totally overprinting the long-wavelength segmentation pattern of the ridge, to that of weaker hotspots, barely marking some of the observables in the ridge axial domain. Intermediate cases are observed, in which hotspots of medium activity (or whose activity has gradually decreased) located at some distance from the ridge axis produce geophysical or geochemical signals whose variation along the axis can be correlated with the geometry of the plume head in the upper mantle. Such observations tend to preclude the use of a single hotspot/ridge interaction model and stress the need for additional observations in various plume/ridge configurations.

  9. Strontium and neodymium isotopes in hot springs on the East Pacific Rise and Guaymas Basin

    NASA Technical Reports Server (NTRS)

    Piepgras, D. J.; Wasserburg, G. J.

    1985-01-01

    Solutions collected from 21 deg N, East Pacific Rise (Epr) and Guaymas Basin, Gulf of California, are analyzed for Nd isotopic composition and Sm and Nd concentrations. The results indicate extensive but not complete isotopic exchange with Sr in the depleted oceanic crust and that Sr concentrations in these solutions are buffered. In contrast, the Nd data exhibit a wide range in isotopic composition and concentration between vents. Many samples show substantial contributions from MORB, but all have isotopic compositions below MORB, in spite of enrichments in Nd up to 100 times seawater. It is shown that the fluids must exchange Nd with a sedimentary reservoir having an isotopic composition less than Pacific seawater. Low-temperature reactions with metalliferous sediments on the flanks of the EPR may provide such a source. Using a simple box method, estimates of the hydrothermal fluxes of Nd are compared to fluxes which are necessary to maintain a radiogenic isotopic composition of about -3 in the Pacific against the influx of Antarctic waters. It is concluded that erosion from island arcs is the main source of radiogenic Nd in the Pacific.

  10. NWA 7034 Martian Breccia: Disturbed Rb-Sr Systematics, Preliminary Is Approximately 4.4 Ga Sm-Nd Age

    NASA Technical Reports Server (NTRS)

    Nyquist, L. E.; Shih, C.-Y.; Peng, Zhan Xiong; Agee, C

    2013-01-01

    Agee et al. [1] reported a Rb-Sr age of 2.089 [plus or minus] 0.081 Ga for the unique Martian meteoritic breccia NWA 7034 making it the oldest Martian basalt, dating to the early Am-azonian epoch [2] of Martian geologic history. We have attempt-ed to confirm this exciting result. Our new Rb-Sr analyses show the Rb-Sr isotopic system to be disturbed, but preliminary Sm-Nd data suggest an even older age of approximately 4.4 Ga for at least some brec-cia components.

  11. Rb-Sr, Sm-Nd and Lu-Hf isotope systematics of the lunar Mg-suite: the age of the lunar crust and its relation to the time of Moon formation

    PubMed Central

    Carlson, Richard W.; Borg, Lars E.; Gaffney, Amy M.; Boyet, Maud

    2014-01-01

    New Rb-Sr, 146,147Sm-142,143Nd and Lu-Hf isotopic analyses of Mg-suite lunar crustal rocks 67667, 76335, 77215 and 78238, including an internal isochron for norite 77215, were undertaken to better define the time and duration of lunar crust formation and the history of the source materials of the Mg-suite. Isochron ages determined in this study for 77215 are: Rb-Sr=4450±270 Ma, 147Sm-143Nd=4283±23 Ma and Lu-Hf=4421±68 Ma. The data define an initial 146Sm/144Sm ratio of 0.00193±0.00092 corresponding to ages between 4348 and 4413 Ma depending on the half-life and initial abundance used for 146Sm. The initial Nd and Hf isotopic compositions of all samples indicate a source region with slight enrichment in the incompatible elements in accord with previous suggestions that the Mg-suite crustal rocks contain a component of KREEP. The Sm/Nd—142Nd/144Nd correlation shown by both ferroan anorthosite and Mg-suite rocks is coincident with the trend defined by mare and KREEP basalts, the slope of which corresponds to ages between 4.35 and 4.45 Ga. These data, along with similar ages for various early Earth differentiation events, are in accord with the model of lunar formation via giant impact into Earth at ca 4.4 Ga. PMID:25114305

  12. Along-arc distribution of 3He/4He and 87Sr/86Sr in thermal fluids of the Kuril Island arc (Russia)

    NASA Astrophysics Data System (ADS)

    Taran, Y.; Kalacheva, E.; Bujakajte, M.; Inguaggiato, S.

    2017-12-01

    The Kuril Island arc in the NW Pacific extends for 1200 km from the Kamchatka Peninsula to Hokkaido Islandand separates the margin Sea of Okhotsk from the Pacific Ocean. Among 40 active volcanoes at least 7 are characterized by strong and high-temperature fumarolic activity, 1 to 3 volcanoes are erupting right now, and many of active and dormant volcanoes host hydrothermal systems. We report our data on hydrochemistry and isotopic composition of He and Sr from fumarolic and hydrothermal discharges sampled along the arc, from Ebeko volcano on Paramushir Island to Golovnin volcano on Kunashir Island. The data were obtained during the field campaign in 2015-2017. Most of hydrothermal systems of Kuril Islands discharge acid-to-ultra acid SO4-Cl and Cl-SO4 waters and steam-heated SO4 waters. On some islands, like Shiashkotan, northern Kurils, coastal hot springs can be found issuing Na-Cl waters mixed with seawater. Mature Na-Cl waters are known only on southern big islands Iturup and Kunashir. The distribution of 3He/4He in hydrothermal and fumarolic gases along the arc is very uniform with 3He/4He values close to the MORB value of 8Ra where Ra is atmospheric ratio (1.4 x 10-6). The northernmost Ebeko volcano discharges fumaroles with 3He/4He up to 7.9Ra, and bubbling gas in the nearest hot springs up to 7.6Ra. Such high 3He/4He values with a maximum of 8.3Ra in fumaroles of the Pallas Peak in the middle of the arc were measured in all thermal manifestations of the arc (fumaroles, hydrothermal steam vents and bubbling gases) up to the southernmost Kunashir Island, where volcanic and hydrothermal gases are characterized by significantly lower values of 5.5Ra at Mendeleev volcano and 3.5Ra at Golovnin volcano. Isotopic ratio of the dissolved Sr as a rule corresponds to the 87Sr/86Sr values of the host rocks and only in the coastal hot springs demonstrates partial mixing with seawater. There is also a general consistence of 87Sr/86Sr in springs and 3He/4He in gases. This

  13. Tectonic controls on the long-term carbon isotope mass balance.

    PubMed

    Shields, Graham A; Mills, Benjamin J W

    2017-04-25

    The long-term, steady-state marine carbon isotope record reflects changes to the proportional burial rate of organic carbon relative to total carbon on a global scale. For this reason, times of high δ 13 C are conventionally interpreted to be oxygenation events caused by excess organic burial. Here we show that the carbon isotope mass balance is also significantly affected by tectonic uplift and erosion via changes to the inorganic carbon cycle that are independent of changes to the isotopic composition of carbon input. This view is supported by inverse covariance between δ 13 C and a range of uplift proxies, including seawater 87 Sr/ 86 Sr, which demonstrates how erosional forcing of carbonate weathering outweighs that of organic burial on geological timescales. A model of the long-term carbon cycle shows that increases in δ 13 C need not be associated with increased organic burial and that alternative tectonic drivers (erosion, outgassing) provide testable and plausible explanations for sustained deviations from the long-term δ 13 C mean. Our approach emphasizes the commonly overlooked difference between how net and gross carbon fluxes affect the long-term carbon isotope mass balance, and may lead to reassessment of the role that the δ 13 C record plays in reconstructing the oxygenation of earth's surface environment.

  14. Asthenospheric and lithospheric sources for Mesozoic dolerites from Liberia (Africa): trace element and isotopic evidence

    NASA Astrophysics Data System (ADS)

    Dupuy, C.; Marsh, J.; Dostal, J.; Michard, A.; Testa, S.

    1988-01-01

    Combined elemental, and Sr and Nd isotopic data are presented for Mesozoic dolerite dikes of Liberia (Africa) which are related to the initial stage of opening of the Atlantic Ocean. The large scatter of both trace element and isotopic data allows the identification of five groups of dolerites which cannot be related to each other by simple processes of mineral fractionation from a common source. On the contrary, the observed chemical and isotopic variation within some dolerites (Groups I and II) may result either from variable degrees of melting of an isotopically heterogeneous source or mixing between enriched and depleted oceanic type mantle. For the other dolerites (Groups III-V) mixing with a third mantle source with more radiogenic Sr and with element ratios characteristic of subduction environments is suggested. This third source is probably the subcontinental lithospheric mantle. Finally, no significant modification by interaction with continental crust is apparent in most of the analyzed samples.

  15. Identification of the geographical place of origin of an unidentified individual by multi-isotope analysis.

    PubMed

    Font, Laura; van der Peijl, Gerard; van Leuwen, Carina; van Wetten, Isis; Davies, Gareth R

    2015-01-01

    A multi-isotope investigation (Sr and Pb isotopes and δ18O, δ13C and δ15N) was applied to bone and teeth from an unidentified male found drowned in the"IJ" Ruyterkade in Amsterdam, The Netherlands in March of 1999. The individual remained unidentified until mid 2013, after the isotope study was completed. Coupled δ13C and δ15N values in bone collagen recovered from rib and femur are consistent with an omnivore living in a region where C3-type diet dominates (i.e. Europe). Integrated Sr and Pb isotopes and δ18O values in canine and third molar teeth and femur and rib bone data exclude extended residence in north-west Europe and particularly The Netherlands. Characteristic Pb isotope ratios coupled with inferred δ18O values of drinking water argue for a most probable place of origin for the unidentified individual in west and south Poland, south-east Slovakia and the region of Ukraine-Romania-Bulgaria, specifically the region associated with the Carpathian Mountains. Independent of the isotope study, the Cold Case Team made a positive identification with an individual from south-west Poland, validating the results of the multiple-isotopic approach. Copyright © 2014 Forensic Science Society. Published by Elsevier Ireland Ltd. All rights reserved.

  16. Evidence for a late thermal event of unequilibrated enstatite chondrites: a Rb-Sr study of Qingzhen and Yamato 6901 (EH3) and Khairpur (EL6)

    USGS Publications Warehouse

    Torigoye, N.; Shima, M.

    1993-01-01

    The Rb-Sr whole rock and internal systematics of two EH3 chondrites, Qingzhen and Yamato 6901, and of one EL6 chondrite, Khairpur, were determined. The internal Rb-Sr systematics of the EH3 chondrites are highly disturbed. Fractions corresponding to sulfide phases show excess 87Sr, while other fractions corresponding to silicate phases produce a linear trend on a Rb-Sr evolution diagram. If these linear relations are interpreted as isochrons, the ages of the silicate phases are 2.12?? 0.23 Ga and 2.05 ??0.33 Ga with the initial Sr isotopic ratios of 0.7112 ?? 0.0018 and 0.7089 ?? 0.0032, for Qingzhen and Yamato 6901, respectively. The Rb-Sr results are interpeted as indicative of a late thermal event about 2Ga ago on the parent bodies of these EH3 chondrites. These ages agree well with previously published K-Ar ages. An older isochron age of 4.481 ?? 0.036 Ga with a low initial Sr isotopic ratio of 0.69866 ?? 0.00038 was obtained for the data from silicate fractions of Khairpur, indicating early petrological equilibrium on the parent body of EL6 chondrites. -from Authors

  17. 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

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Grottoli, A.; Adkins, J; Panero, W

    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 appearmore » 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.« less

  18. A reconnaissance study of oxygen, hydrogen and strontium isotopes in geochemically diverse lakes, Western Nebraska, USA

    USGS Publications Warehouse

    Gosselin, D.C.; Nabelek, P.E.; Peterman, Z.E.; Sibray, S.

    1997-01-01

    Reconnaissance ??18O,, ??D, and ??87Sr data for fifteen lakes in the Western Lakes Region of the Sand Hills of Nebraska indicate dynamic hydrologic systems. The rather narrow range of ??87Sr from lake water (1.1 to 2.1) and groundwater (0.9 to 1.7) indicates that the groundwater is generally unradiogenic. Groundwater residence times and relatively unradiogenic volcanic ash within the dune sediments control the ??87Sr values. Based on the mutual variations of ??18O and ??D, the lakes can be divided into three groups. In Group 1, both ??18O and ??D values increase from spring to fall. The ??18O and ??D values in Group 2 decreased from spring to fall. Group 3 are ephemeral lakes that went dry some time during 1992. The data and isotopic modeling show that variations in the ratio of evaporation relative to groundwater inflow, local humidity conditions, and the ??(a) has substantial influence on the isotopic composition. In addition, isotopic behavior in ephemeral hakes can be rather unusual because of the changing activities of water and mineral precipitation and redissolution. The annual and interannual isotopic variability of these lakes which is reflected in the paleonvironmental indicators may be the rule rather than the exception in these types of systems.

  19. Kiglapait Feldspar States 5 to <2 Kbar, 1250 to 240 Degrees C in 20 Ma: Liquidus, Solidus, Solvi, and Subsolidus with Sr Isotope Partitioning: a Review

    NASA Astrophysics Data System (ADS)

    Morse, S. A.

    2017-12-01

    The 1305 Ga Kiglapait Intrusion of coastal Labrador records the crystallization of troctolite through olivine gabbro to magnetite- and apatite-bearing rocks to monoclinic sanidine- mesoperthite-ferrosyenite below an inverted stratigraphy of a thin Upper Border Zone. The crystallization history was about 1 Ma. ¶The evolutionary history of Kiglapait feldspars in an 8.4 km thick magma chamber runs from plagioclase An70 at 5 kbar and 1250°C, cooling through to ferrosyenite with mesoperthite and two feldspars at 3 kbar and 1,000°C. The residual magma encountered the binodal solvus and finished crystallizing as an azeotrope with plagioclase (Or 21, An 15) and sanidine (Or 52, An 8) in liquid (Xor = 1/3; An 11). Cooling in the subsolidus brought the feldspars to compositions An15-Or 3, An0-Or 80-85 at 800-730°C. Metastable mesoperthite on the coherent solvus in various stages of late equilibration persists in the local assemblages. Arrested to complete feldspar symplectites suggest the local presence of a vapor phase. ¶Splits of the final Or-rich feldspar were found by mass spectrometry to have a dominant quantity of Rb and 87Sr/86Sr along with % amounts of Ba; in contrast, the plag fraction has very low Rb and 87Sr/86Sr. The estimated timing of the isotopic segregation was plausibly continuous with major-element fractionation or perhaps at the moment(s) of exsolution. ¶The cooling record of the solidified intrusion at 3 kbar is shown by 40Ar/39Ar data to have been rapid, reaching an ambient temperature near 240°C within the first 20 Ma, compared to the ambient country-rock temperature before intrusion of 350°C. The difference suggests a late uplift of the region after the Kiglapait magmatism. ¶Contributions from Y. Yu, T. Krogh, M. Hamilton, D. Lindsley, D. DePaolo, M. Jercinovic and S.R. Hart are especially acknowledged.

  20. 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

    NASA Astrophysics Data System (ADS)

    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 (0.70406-0.70461) and moderate ɛ Nd (300 Ma) (-0.9 to 1.5) for the GD and LG, and relatively high ɛ Hf (300 Ma) values (-3.6 to +11.2) for the GD, suggesting the magma mainly originated from the juvenile lower crust that was derived from depleted mantle, with a minor component of ancient continental crust. Lead isotope data have characteristics of a lower crust source with minor contamination by upper crustal material. Combined with previous research, the Zhunsujihua granitoid intrusions developed in an intracontinental volcanic arc (Uliastai) associated with northward subduction of the Paleo-Asian Ocean plate during late Carboniferous to early Permian; this suggests