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Sample records for 87sr 86sr ratio

  1. 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.

  2. 87Sr/86Sr ratios in basalts from islands in the Indian Ocean

    USGS Publications Warehouse

    Hedge, C.E.; Watkins, N.D.; Hildreth, R.A.; Doering, W.P.

    1973-01-01

    87Sr/86Sr ratios of basalts from islands in the Indian Ocean (0.7040) are higher than those of basalts dredged from the Mid-Indian Ocean Ridge (0.7034). The sources of the island basalts have apparently not been in equilibrium with the source of the ridge basalts for roughly 109 years. Both ridge and island basalts in the Indian Ocean are higher in 87Sr/86Sr than are rocks from similar settings in the eastern Pacific. ?? 1973.

  3. Alteration histories of fossil biogenic calcite as indicated by 87Sr/86Sr ratios

    NASA Astrophysics Data System (ADS)

    Ullmann, C. V.; Campbell, H. J.; Korte, C.

    2012-04-01

    The 87Sr/86Sr, δ18O and δ13C composition of biogenic calcite from stratigraphically well-defined marine fossils can be utilized to reconstruct paleoenvironments and the isotopic evolution of past seawater. A conceptual prerequisite for reliable results is a minimum of post-depositional alteration of the samples. In order to establish a measure of the degree of alteration it is common practise to check all biogenic calcite samples using cathodoluminescence, SEM, and trace element concentration analysis. However, none of these screening techniques is fool-proof. A combination of these approaches is necessary to select the best preserved samples. In this study we show that strontium isotope signatures can serve as an independent alteration indicator. Because the seawater 87Sr/86Sr ratio in fully marine environments is virtually constant during the lifespan (< 50 years) of the shelly organisms involved, and biofractionation of the 87Sr/86Sr ratio is corrected for by the recalculation to a constant 88Sr/86Sr of 0.1194, only altered samples exhibit variability of the 87Sr/86Sr ratio beyond analytical reproducibility and/or significant deviation from the strontium isotope curve for seawater. We measured 87Sr/86Sr, δ18O, δ13C and element ratios from a Late Kimmeridgian belemnite from New Zealand, and a Late Triassic (Rhaetian) brachiopod from New Caledonia. The 87Sr/86Sr ratios for the belemnite vary from 0.706724 to 0.706928 (n = 5) with three values being compatible with coeval seawater and two values being less radiogenic than the lowest seawater value of the Phanerozoic seawater curve. The low 87Sr/86Sr ratios coincide with elevated Mn and low Sr concentrations, and light δ18O values indicate diagenesis that involved fluids leaching less radiogenic Sr from the surrounding rocks, and re-crystallisation of the belemnite guard at elevated temperatures. The 87Sr/86Sr ratios of the brachiopod vary from 0.707813 to 0.707934 (n = 8) and are strongly correlated with Mg

  4. 87Sr 86Sr ratios for basalt from Loihi Seamount, Hawaii

    USGS Publications Warehouse

    Lanphere, M.

    1983-01-01

    87Sr 86Sr ratios of 15 samples of basalt dredged from Loihi Seamount range from 0.70334 to 0.70368. The basalt types range from tholeiite to basanite in composition and can be divided into six groups on the basis of abundances of K2O, Na2O, Rb and Sr and 87Sr 86Sr ratio. The isotopic data require that the various basalt types be derived from source regions differing in Sr isotopic composition. The Loihi basalts may be produced by mixing of isotopically distinct sources, but the tholeiites and alkalic basalts from Loihi do not show a well-developed inverse trend between Rb/Sr and 87Sr 86Sr that is characteristic of the later stages of Hawaiian volcanoes such as Haleakala and Koolau. ?? 1983.

  5. 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

  6. 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

  7. Quantifying Saline Groundwater Discharge to the Rio Grande using 87Sr/86Sr and [Ca]/[Sr] Ratios

    NASA Astrophysics Data System (ADS)

    Hogan, J. F.; Phillips, F. M.; Mills, S. K.; Ruiz, J.; Chesley, J. T.

    2002-12-01

    Issues of water quality, especially salinity, limit the use of water resources from the Rio Grande. Identification and quantification of salinity sources is critical for improved river management. We have conducted winter and summer synoptic sampling of the Rio Grande from the headwaters in Colorado to south of El Paso, Texas. The total dissolved solids content (TDS) of the Rio Grande increases from less than 50 mg/L in headwater regions of Colorado to greater than 2000 mg/L south of El Paso, Texas. Increases in salinity are not a simple function of distance downriver, but rather occur in a series of steps. Many of these increases are located at the lower end of sedimentary basins leading to the hypothesis that they are the result of discharge of deep, saline, groundwaters. Of particular interest is the Albuquerque and Socorro basins where, in three distinct steps, the TDS of the river doubles from ~ 150 mg/L to ~ 300 mg/L. With little change in river discharge for this reach, this represents a significant increase in the solute burden of the river. We have used 87Sr/86Sr and [Ca]/[Sr] ratios to "fingerprint" and quantify saline groundwater discharge. The Rio Grande entering the Albuquerque basin has an 87Sr/86Sr ratio of 0.7096and a [Ca]/[Sr] ratio of 80. These values are consistent with a mixture of atmospheric deposition and weathering of basalt rock found upstream. Traveling through the Albuquerque and Socorro basin the Rio Grande shifts to a 87Sr/86Sr ratio of 0.7102 and a [Ca]/[Sr] ratio of 30, values which are consistent with saline groundwater discharge. Mixing relationships indicate only two solute sources are required, and that a total saline groundwater discharge rate of ~ 50 cfs is sufficient to explain the observed salinity increases.

  8. 87Sr/ 86Sr ratios in modern and fossil food-webs of the Sterkfontein Valley: implications for early hominid habitat preference

    NASA Astrophysics Data System (ADS)

    Sillen, Andrew; Hall, Grant; Richardson, Stephen; Armstrong, Richard

    1998-07-01

    This research addresses the potential contribution of strontium isotopes to the reconstruction of early hominid behavior at the Swartkrans site in the Sterkfontein Valley of Gauteng Provence (formally known as the Transvaal), South Africa. We report that, while there is considerable variability in the 87Sr/ 86Sr of whole soils within a 15 km radius of this site, available soil and grassland plant 87Sr/ 86Sr is much less variable and generally above 0.730. This value is higher (more radiogenic) than the 87Sr/ 86Sr of plants growing within the greenbelt surrounding the Blaaubank stream adjacent to Swartkrans and streamwater itself (0.721). The difference between grassland and riparian strontium isotope composition suggests a method for determining habitat utilization by early hominids. In this study, a geological explanation for a natural difference between Blaaubank stream and grassland Sr is suggested, based on relatively less radiogenic Sr (having lower 87Sr/ 86Sr values) in the carbonate component of the local dolomite when compared to other nearby geological formations. The explanation was tested initially using a top-down approach in which the 87Sr/ 86Sr ratios of water, soil, and plants from the entire Blaaubank catchment were measured. Next, a bottom-up approach was used to examine Swartkrans Member I faunal species known to have obtained their Sr from well-defined habitats. The results are that (1) pollution is not the explanation for the relatively low 87Sr/ 86Sr ratios of the Blaaubank stream, (2) Swartkrans Member I carbonate has a similar 87Sr/ 86Sr to that of modern Blaaubank water, indicating that relationships seen today existed in the Pleistocene, and (3) Pleistocene riparian fauna have relatively low 87Sr/ 86Sr ratios when compared to fauna adapted to drier habitats. Together these results make it possible to interpret the strontium isotope composition of Pleistocene early hominids from Swartkrans in terms of habitat utilization.

  9. Quantifying sediment sources in a lowland agricultural catchment pond using (137)Cs activities and radiogenic (87)Sr/(86)Sr ratios.

    PubMed

    Le Gall, Marion; Evrard, Olivier; Foucher, Anthony; Laceby, J Patrick; Salvador-Blanes, Sébastien; Thil, François; Dapoigny, Arnaud; Lefèvre, Irène; Cerdan, Olivier; Ayrault, Sophie

    2016-10-01

    Soil erosion often supplies high sediment loads to rivers, degrading water quality and contributing to the siltation of reservoirs and lowland river channels. These impacts are exacerbated in agricultural catchments where modifications in land management and agricultural practices were shown to accelerate sediment supply. In this study, sediment sources were identified with a novel tracing approach combining cesium ((137)Cs) and strontium isotopes ((87)Sr/(86)Sr) in the Louroux pond, at the outlet of a lowland cultivated catchment (24km(2), Loire River basin, France) representative of drained agricultural areas of Northwestern Europe. Surface soil (n=36) and subsurface channel bank (n=17) samples were collected to characterize potential sources. Deposited sediment (n=41) was sampled across the entire surface of the pond to examine spatial variation in sediment deposits. In addition, a 1.10m sediment core was sampled in the middle of the pond to reconstruct source variations throughout time. (137)Cs was used to discriminate between surface and subsurface sources, whereas (87)Sr/(86)Sr ratios discriminated between lithological sources. A distribution modeling approach quantified the relative contribution of these sources to the sampled sediment. Results indicate that surface sources contributed to the majority of pond (μ 82%, σ 1%) and core (μ 88%, σ 2%) sediment with elevated subsurface contributions modeled near specific sites close to the banks of the Louroux pond. Contributions of the lithological sources were well mixed in surface sediment across the pond (i.e., carbonate sediment contribution, μ 48%, σ 1% and non-carbonate sediment contribution, μ 52%, σ 3%) although there were significant variations of these source contributions modeled for the sediment core between 1955 and 2013. These fluctuations reflect both the progressive implementation of land consolidation schemes in the catchment and the eutrophication of the pond. This original sediment

  10. Quantifying sediment sources in a lowland agricultural catchment pond using (137)Cs activities and radiogenic (87)Sr/(86)Sr ratios.

    PubMed

    Le Gall, Marion; Evrard, Olivier; Foucher, Anthony; Laceby, J Patrick; Salvador-Blanes, Sébastien; Thil, François; Dapoigny, Arnaud; Lefèvre, Irène; Cerdan, Olivier; Ayrault, Sophie

    2016-10-01

    Soil erosion often supplies high sediment loads to rivers, degrading water quality and contributing to the siltation of reservoirs and lowland river channels. These impacts are exacerbated in agricultural catchments where modifications in land management and agricultural practices were shown to accelerate sediment supply. In this study, sediment sources were identified with a novel tracing approach combining cesium ((137)Cs) and strontium isotopes ((87)Sr/(86)Sr) in the Louroux pond, at the outlet of a lowland cultivated catchment (24km(2), Loire River basin, France) representative of drained agricultural areas of Northwestern Europe. Surface soil (n=36) and subsurface channel bank (n=17) samples were collected to characterize potential sources. Deposited sediment (n=41) was sampled across the entire surface of the pond to examine spatial variation in sediment deposits. In addition, a 1.10m sediment core was sampled in the middle of the pond to reconstruct source variations throughout time. (137)Cs was used to discriminate between surface and subsurface sources, whereas (87)Sr/(86)Sr ratios discriminated between lithological sources. A distribution modeling approach quantified the relative contribution of these sources to the sampled sediment. Results indicate that surface sources contributed to the majority of pond (μ 82%, σ 1%) and core (μ 88%, σ 2%) sediment with elevated subsurface contributions modeled near specific sites close to the banks of the Louroux pond. Contributions of the lithological sources were well mixed in surface sediment across the pond (i.e., carbonate sediment contribution, μ 48%, σ 1% and non-carbonate sediment contribution, μ 52%, σ 3%) although there were significant variations of these source contributions modeled for the sediment core between 1955 and 2013. These fluctuations reflect both the progressive implementation of land consolidation schemes in the catchment and the eutrophication of the pond. This original sediment

  11. 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.

  12. Determination of the 87Sr/86Sr isotope ratio in USGS silicate reference materials by multi-collector ICP-mass spectrometry

    NASA Astrophysics Data System (ADS)

    Balcaen, Lieve; Schrijver, Isabel De; Moens, Luc; Vanhaecke, Frank

    2005-04-01

    Multi-collector ICP-mass spectrometry (MC-ICP-MS) was used for 87Sr/86Sr isotope ratio determination in newly introduced silicate reference materials from the US Geological Survey (USGS): granite G-3, andesite AGV-2, and basalt BCR-2. Next to the SrCO3 isotopic standard NIST SRM 987, also analogous USGS reference materials from the previous generation, and for which reference 87Sr/86Sr data obtained by TIMS are available, were analysed for validation purposes. Sample preparation consisted of acid digestion and subsequent isolation of Sr by means of a dedicated and commercially available crown ether-based resin. The Sr fractions thus obtained were analysed via MC-ICP-MS whereby mass discrimination was corrected for internally, while the isobaric interference at a mass-to-charge ratio of 86 caused by Kr impurities in the Ar gas was mathematically corrected for by using the signal for a Kr isotope free from spectral overlap. Finally, also the effect of the small amount of Rb that may still be present in the Sr fraction was corrected for mathematically on the basis of the signal intensity for 85Rb. The MC-ICP-MS results for G-2, AGV-1 and BCR-1 showed an excellent agreement with the corresponding TIMS values (<0.003% bias in all cases), such that it can be assumed that also the 87Sr/86Sr isotope ratio results obtained for the new reference materials are reliable.

  13. Migration and mobility in the early medieval settlement in Thunau/Kamp using 87Sr/86Sr Isotope ratio measurements by MC-ICPMS

    NASA Astrophysics Data System (ADS)

    Gangl, Sophie; Irrgeher, Johanna; Teschler-Nicola, Maria; Prohaska, Thomas

    2013-04-01

    The use of Sr isotope ratios has been applied systematically for clarifying questions about migration patterns of humans and animals. In consequence of geologically induced differences in the isotopic composition, 87Sr/86Sr ratios are characteristic for a specific region. Humans and animals take up strontium primarily via drinking water and diet. Since strontium has similar chemical properties to calcium, it is mainly stored in teeth and bones. Tooth enamel is formed in the early childhood and is not subject to significant changes in later life. Therefore, the enclosed strontium has the same isotopic composition as the environment in which the individual was living during his early years, provided that the food came from the close proximity. Issue of this study was the early medieval (9th to 10th century AD) settlement in Thunau/Kamp. In order to assess the biogenic Sr isotopic signature of the Thunau settlement area, environmental samples including soil, rocks, water and plants were taken at the excavation site and in the immediate vicinity. They represent the local strontium signal to which the isotopic compositions of historic human tooth samples (enamel and dentine) were compared. The 87Sr/86Sr ratios in tooth enamel and dentine give insight about residential characteristics of the settlement of Thunau/Kamp in comparison to the fortified hilltop settlement located in close proximity.

  14. Natural variation of 87Sr/86Sr in coral Porites from southern Taiwan

    NASA Astrophysics Data System (ADS)

    Liu, Y.; Chiang, H.; Shen, C.; Lee, D.; Chen, Y.

    2009-12-01

    Monthly resolution 87Sr/86Sr records of living coral Porites heads, collected in Nanwan Bay, southernmost Taiwan (21o55’N, 120o47’E), were analyzed by a MC-ICP-MS at the Department of Geosciences, National Taiwan University. Between the time window of 1992 and 2002, 87Sr/86Sr ratios remained constant at 0.709176 in winter, while strong annual fluctuations between 0.709171 and 0.709203 were observed during the summer. No relationship is found between Sr/Ca and δ18O, which suggests that the effect of temperature and fresh water input are negligible to the observed summer fluctuations of 87Sr/86Sr in these corals. Furthermore, 87Sr/86Sr ratio in offshore water exhibits a significantly offset of 0.00002-0.00003, and which is positively correlated to the variations of the coral values of 0.70917-0.70918. If this is correct, there exists a source that is responsible for the low 87Sr/86Sr observed in the corals, alternatively, a biologically kinetic effect can also explain the data. In order to better constrain the causes of the observed 87Sr/86Sr variations in these corals, a 84Sr-86Sr double-spike method using TIMS is currently being set up, and the data will be presented in this meeting.

  15. 87Sr/86Sr ratios in some eugeosynclinal sedimentary rocks and their bearing on the origin of granitic magma in orogenic belts

    USGS Publications Warehouse

    Peterman, Z.E.; Hedge, C.E.; Coleman, R.G.; Snavely, P.D.

    1967-01-01

    Rb and Sr contents and 87Sr/86Sr values were determined for samples of eugeosynclinal sedimentary rocks, mostly graywackes, from Oregon and California. These data are compatible with the theory of anataxis of eugeosynclinal sedimentary rocks in orogenic belts to produce granitic magmas provided that the melting occurs within several hundreds of m.y. after sedimentation. The low (87Sr/86Sr)0 values of the eugeosynclinal sedimentary rocks are related to the significant amounts of volcanogenic detritus present which probably were originally derived from the mantle. ?? 1967.

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

    PubMed

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

    2016-12-01

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

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

    NASA Astrophysics Data System (ADS)

    Irrgeher, Johanna; Galler, Patrick; Prohaska, Thomas

    2016-11-01

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

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

    PubMed

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

    2016-01-01

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

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

    PubMed

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

    2016-01-01

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

  20. Reassessing the stable (δ88/86Sr) and radiogenic (87Sr/86Sr) strontium isotopic composition of marine inputs

    NASA Astrophysics Data System (ADS)

    Pearce, Christopher R.; Parkinson, Ian J.; Gaillardet, Jérôme; Charlier, Bruce L. A.; Mokadem, Fatima; Burton, Kevin W.

    2015-05-01

    and additional Sr contributions from the bedrock. Together, the principal marine inputs define flux-weighted oceanic δ88/86Srinput and 87Sr/86Srinput compositions of 0.32‰ and 0.71161. These values are consistent with an elevated supply of riverine Sr to the oceans due to increased post-glacial weathering, but require the enhanced weathering of exposed carbonate shelves during glacial periods or significant changes in the rate of carbonate burial to match observed changes in the 87Sr/86Sr ratio of seawater. Our results confirm that, providing a diagenetically robust proxy can be found, the δ88/86Sr and 87Sr/86Sr isotope systems should provide a useful proxy for investigating changes in the marine carbonate system through time.

  1. delta. sup 18 O values, sup 87 Sr/ sup 86 Sr and Sr/Mg ratios of Late Devonian abiotic marine calcite: Implications for the composition of ancient seawater

    SciTech Connect

    Carpenter, S.J.; Lohmann, K.C.; Walter, L.M.; Huston, J.G.; Halliday, A.N. ); Holden, P. )

    1991-07-01

    Late Devonian (Frasnian) abiotic marine calcite has been microsampled and analyzed for {sup 87}Sr/{sup 86}Sr ratios, {delta}{sup 18}O and {delta}{sup 13}C values, and minor element concentrations. Portions of marine cement crystals from the Alberta and Canning Basins have escaped diagenetic alteration and preserve original marine {delta}{sup 18}O values ({minus}4.8{per thousand} {plus minus} 0.5, PDB), {delta}{sup 13}C values (+2.0 to +3.0{per thousand}, PDB), {sup 87}Sr/{sup 86}Sr ratios (0.70805 {plus minus} 3), and Sr/Mg weight ratios (0.04 to 0.05). Marine {sup 87}Sr/{sup 86}Sr ratios are globally consistent and can be correlated within the Alberta Basin, and among the Alberta, Canning, and Williston Basins. Correlation of isotopic and chemical data strengthen the conclusion that marine cements from the Leduc Formation preserve original marine {delta}{sup 18}O values which are 3 to 4{per thousand} lower than those of modern marine cements. These low {delta}{sup 18}O values are best explained by precipitation from {sup 18}O-depleted seawater and not be elevated seawater temperature or diagenetic alteration. For comparison with Devonian data, analogous data were collected from Holocene Mg-calcite and aragonite marine cements from Enewetak Atoll, Marshall Islands. Mg-calcite and aragonite marine cements are in isotopic equilibrium with ambient seawater, and Mg-calcite cements are homogeneous with respect to Sr and Mg contents. Comparison of Sr and Mg contents of analogous Devonian and Holocene marine cements suggests that the Mg/Ca ratio of Late Devonian seawater was significantly lower and that the Sr/Ca ratio was significantly higher than that of modern seawater.

  2. 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.

  3. 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. PMID:27664633

  4. The evolution of the 87Sr/86Sr in the Dead Sea brine: from the Sedom lagoon to Sahara dusts

    NASA Astrophysics Data System (ADS)

    Stein, Mordechai

    2016-04-01

    The history of water-bodies in the Dead Sea brines commenced with the intrusion of the Sedom lagoon, possibly in the late Neogene and continued with the development of hypersaline and freshwater lakes (e.g. the modern Dead Sea and Sea of Galilee). 87Sr/86Sr ratios in these water-bodies decreased over the past ~ 5-6 Ma from 0.7087-0.7084 in salts deposited in the Sedom lagoon to ~ 0.7080 in modern Dead Sea brine. The 87Sr/86Sr ratios in the salts deposited from Sedom lagoon are significantly lower than those of the contemporaneous late Miocene seawater (~0.709). This difference was attributed to modification of the 87Sr/86Sr ratio in the Sedom lagoon solution by influx of Ca-chloride brines. The brines, in turn were formed by dolomitization of marine limestones of the DSR Cretaceous wall rocks (87Sr/86Sr ~ 0.7075) by the ingressing evaporated seawaters (Stein et al., 2000). After the disconnection of the Sedom lagoon from the open sea freshwater filled the lakes that occupied the Dead Sea basin. The freshwater influx modified the strontium isotope and chemical composition of the brine and provided bicarbonate and sulfate to the lake that led the precipitation of primary aragonite and gypsum. Freshwater that currently enter the lake are characterize by 87Sr/86Sr ~ 0.7081, significantly higher than the Cretaceous carbonates. Settled dust that deposits on the Judea Mountains is composed of calcite and quartz grains and is characterized by 87Sr/86Sr ratios ~ 0.7084. It appears that significant amounts of the strontium that entered the lakes with the freshwater originated from dissolution of the dust calcites. Large amounts of dust were transported from the Sahara desert to the Dead Sea watershed during glacial periods when the Sahara was dry and sea-level was low. The source of the detrital calcites however, is not known. They could be derived from dry paleo-lakes in the Sahara that were previously filled by waters that retained the required strontium isotope

  5. Bioavailable 87Sr/86Sr in different environmental samples--effects of anthropogenic contamination and implications for isoscapes in past migration studies.

    PubMed

    Maurer, Anne-France; Galer, Stephen J G; Knipper, Corina; Beierlein, Lars; Nunn, Elizabeth V; Peters, Daniel; Tütken, Thomas; Alt, Kurt W; Schöne, Bernd R

    2012-09-01

    (87)Sr/(86)Sr reference maps (isoscapes) are a key tool for investigating past human and animal migrations. However, there is little understanding of which biosphere samples are best proxies for local bioavailable Sr when dealing with movements of past populations. In this study, biological and geological samples (ground vegetation, tree leaves, rock leachates, water, soil extracts, as well as modern and archeological animal teeth and snail shells) were collected in the vicinity of two early medieval cemeteries ("Thuringians", 5-6th century AD) in central Germany, in order to characterize (87)Sr/(86)Sr of the local biosphere. Animal tooth enamel is not appropriate in this specific context to provide a reliable (87)Sr/(86)Sr baseline for investigating past human migration. Archeological faunal teeth data (pig, sheep/goat, and cattle) indicates a different feeding area compared to that of the human population and modern deer teeth (87)Sr/(86)Sr suggest the influence of chemical fertilizers. Soil leachates do not yield consistent (87)Sr/(86)Sr, and (87)Sr/(86)Sr of snail shells are biased towards values for soil carbonates. In contrast, water and vegetation samples seem to provide the most accurate estimates of bioavailable (87)Sr/(86)Sr to generate Sr isoscapes in the study area. Long-term environmental archives of bioavailable (87)Sr/(86)Sr such as freshwater bivalve shells and tree cores were examined in order to track potential historic anthropogenic contamination of the water and the vegetation. The data obtained from the archeological bivalve shells show that the modern rivers yield (87)Sr/(86)Sr ratios which are similar to those of the past. However, the tree cores registered decreasing (87)Sr/(86)Sr values over time towards present day likely mirroring anthropogenic activities such as forest liming, coal mining and/or soil acidification. The comparison of (87)Sr/(86)Sr of the Thuringian skeletons excavated in the same area also shows that the vegetation

  6. Bioavailable 87Sr/86Sr in different environmental samples--effects of anthropogenic contamination and implications for isoscapes in past migration studies.

    PubMed

    Maurer, Anne-France; Galer, Stephen J G; Knipper, Corina; Beierlein, Lars; Nunn, Elizabeth V; Peters, Daniel; Tütken, Thomas; Alt, Kurt W; Schöne, Bernd R

    2012-09-01

    (87)Sr/(86)Sr reference maps (isoscapes) are a key tool for investigating past human and animal migrations. However, there is little understanding of which biosphere samples are best proxies for local bioavailable Sr when dealing with movements of past populations. In this study, biological and geological samples (ground vegetation, tree leaves, rock leachates, water, soil extracts, as well as modern and archeological animal teeth and snail shells) were collected in the vicinity of two early medieval cemeteries ("Thuringians", 5-6th century AD) in central Germany, in order to characterize (87)Sr/(86)Sr of the local biosphere. Animal tooth enamel is not appropriate in this specific context to provide a reliable (87)Sr/(86)Sr baseline for investigating past human migration. Archeological faunal teeth data (pig, sheep/goat, and cattle) indicates a different feeding area compared to that of the human population and modern deer teeth (87)Sr/(86)Sr suggest the influence of chemical fertilizers. Soil leachates do not yield consistent (87)Sr/(86)Sr, and (87)Sr/(86)Sr of snail shells are biased towards values for soil carbonates. In contrast, water and vegetation samples seem to provide the most accurate estimates of bioavailable (87)Sr/(86)Sr to generate Sr isoscapes in the study area. Long-term environmental archives of bioavailable (87)Sr/(86)Sr such as freshwater bivalve shells and tree cores were examined in order to track potential historic anthropogenic contamination of the water and the vegetation. The data obtained from the archeological bivalve shells show that the modern rivers yield (87)Sr/(86)Sr ratios which are similar to those of the past. However, the tree cores registered decreasing (87)Sr/(86)Sr values over time towards present day likely mirroring anthropogenic activities such as forest liming, coal mining and/or soil acidification. The comparison of (87)Sr/(86)Sr of the Thuringian skeletons excavated in the same area also shows that the vegetation

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

    SciTech Connect

    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 the 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.

  8. K, Rb, Sr and 87Sr 86Sr in rocks from the Mid-Indian Oceanic Ridge

    USGS Publications Warehouse

    Subbarao, K.V.; Hedge, C.E.

    1973-01-01

    The 87Sr 86Sr ratios of Mid-Indian Oceanic Ridge (MIOR) basalts are nearly identical (0.7032 to 0.7035), with the exception of one more highly radiogenic sample (0.7043). These values are consistently higher than the strontium isotopic ratios of the ridge basalts from Atlantic and Pacific Oceans, suggesting that the source of the MIOR basalts was depleted in alkalies more recently and/or to a lesser degree than the basalts from other oceans. ?? 1973.

  9. A revised 87Sr/86Sr curve for the Silurian: Implications for global ocean chemistry and the Silurian timescale

    USGS Publications Warehouse

    Cramer, Bradley D.; Munnecke, Axel; Schofield, D.I.; Haase, K.M.; Haase-Schramm, A.

    2011-01-01

    Recent recalibration of the Silurian timescale and improved global chronostratigraphic correlation of Silurian strata significantly altered the Silurian 87Sr/86Sr curve and the temporal extent of available data. Whereas previous Silurian 87Sr/86Sr composites showed a generally monotonic increase throughout the Silurian, revisions to the Silurian timescale now require a major increase in the rate of change in 87Sr/86Sr at or near the onset of the Gorstian Age of the Ludlow Epoch. Similarly, improved chronostratigraphic correlations between Silurian outcrops on Anticosti Island, Canada, and Gotland, Sweden, indicate that the middle part of the Telychian Age, which is roughly 10%-15% of the total duration of the Silurian period, is undersampled and underrepresented in Silurian 87Sr/86Sr composites. A revised Silurian 87Sr/86Sr curve based on 241 new and published analyses confirms the significant increase in the rate of change of 87Sr/86Sr toward more radiogenic values near the base of the Ludlow Series. On the basis of these data, we propose that the rapid trend toward more radiogenic 87Sr/86Sr values is indicative of increased weathering of old sialic crust exposed during the Silurian uplift of portions of Baltica, Laurentia, and Avalonia. Importantly, however, the actual rate of change of 87Sr/86Sr will remain equivocal until the durations of Silurian epochs and ages are better constrained. ?? 2011 by The University of Chicago. All rights reserved.

  10. The applicability of an 87Sr/86Sr river isoscape to fish ecological questions in the Danube catchment

    NASA Astrophysics Data System (ADS)

    Zitek, A.; Irrgeher, J.; Sailer, K.; Trautwein, C.; Waidbacher, H.; Prohaska, T.

    2012-04-01

    Isoscapes are spatial maps of the distribution of isotopes on Earth. As a basis for ecological studies such as long distance migrations of animals or for determining the origin of food these tools are increasingly being developed, until now - mainly for terrestrial systems. In contrast, in case of aquatic systems only few maps were established up to now. As far as variation in the isotopic distribution in a studied area exists, the isotopic composition bears the potential to be used as natural tracer e.g. for ecological questions or food authentication. Above all the 87Sr/86Sr ratio taken up from the environment by organisms without any significant fractionation is known to provide a direct link to geologically distinct regions. Within the 'IsoMark' project (www.isomark.at), a database ('Isoscape Austria') containing all available spatially explicit isotope data (terrestrial and aquatic) with a focus on isotope distributions in Austrian rivers is being developed. Water samples from different rivers, mainly along the Danube in Austria, were collected and analyzed for their elemental and Sr isotopic composition. Analyses of water samples yielded several 'Isozones' along the Austrian part of the Danube, indicating diverse geology in these river catchments. Studying migration phenomena of fish using natural isotopic marks in hard parts is especially possible between these 'Isozones'. In geologically similar regions with little differences, element distributions or artificial marking methods (tagging, spiking) can serve as additional means. A significant positive relationship between the 87Sr/86Sr ratio in river water and the proportion of siliceous geological formations in the catchment was found on a national and European level. These analyses proved the possibility to predict the 87Sr/86Sr ratios in river catchments all over Europe. This relationship allows for an estimation of the applicability of the 87Sr/86Sr ratio for fish ecological questions on a European scale

  11. 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.

  12. Lacustrine 87Sr/86Sr as a tracer to reconstruct Milankovitch forcing of the Eocene hydrologic cycle

    NASA Astrophysics Data System (ADS)

    Baddouh, M'bark; Meyers, Stephen R.; Carroll, Alan R.; Beard, Brian L.; Johnson, Clark M.

    2016-08-01

    The Green River Formation (GRF) provides one of the premier paleoclimate archives of the Early Eocene Climatic Optimum (∼50 Ma), representing the apex of the early Cenozoic greenhouse climate. Rhythmic lake-level variability expressed in the GRF has inspired numerous hypotheses for the behavior of the Eocene hydrologic cycle, including its linkage to astronomical forcing, solar variability, and the El Niño Southern Oscillation (ENSO). However, the lack of sufficient proxy data to document atmospheric water-mass transport and the geographic pattern of evaporation/precipitation/runoff has made it difficult to discriminate between different models for astronomical forcing. Variable 87Sr/86Sr ratios of bedrock that encompass the GRF provide an opportunity to reconstruct the spatial expression of the Eocene hydrologic cycle and its linkage to lake level. Here Sr isotope data from the Wilkins Peak Member, a rhythmic succession that has been demonstrated to record Milankovitch forcing of lake levels, indicate that high lake levels reflect an increased proportion of runoff from less radiogenic rocks west of the basin, eliminating a number of the existing astronomical-forcing hypotheses. The 87Sr/86Sr variability is consistent with a change in mean ENSO state, which is predicted by climate models to be linked to orbital-insolation. Thus, the 87Sr/86Sr data reveal a coupling of high frequency (ENSO) and low frequency (astronomical) climate variability, and also predict the existence of sizable astronomically-forced alpine snowpack during the last greenhouse climate. More broadly, this study demonstrates the utility of 87Sr/86Sr as a powerful tool for reconstructing the deep-time hydrologic cycle.

  13. The petrogenesis of island arc basalts from Gunung Slamet volcano, Indonesia: Trace element and 87Sr /86Sr contraints

    NASA Astrophysics Data System (ADS)

    Vukadinovic, Danilo; Nicholls, Ian A.

    1989-09-01

    Selected major and trace elements, rare earth element (REE) and 87Sr /86Sr data are presented for arc basalts from Gunung Slamet volcano, Java, Indonesia. On the basis of stratigraphy, trace element content, Zr/Nb, and 87Sr /86Sr ratios, Slamet basalts can be broadly categorized into high abundance magma (HAM) and low abundance magma (LAM) types. Provided the quantities of 'immobile' trace elements (in aqueous systems) such as Nb, Hf and Zr in the mantle wedge and ensuing magmas are unaffected by additions from subducted lithosphere or overlying arc crust, a model may be developed whereby LAM are generated by higher degrees of melting in the mantle wedge (13%) compared to HAM (7%). Hf/Nb or Zr/Nb ratio systematics indicate that prior to metasomatism by the underlying lithosphere, the Slamet mantle wedge was similar in chemical character to transitional-MORB source mantle. Conversely, examination of immobile/mobile incompatible trace element ratios (IMITER) provide clues to the nature of the metasomatizing agent, most likely derived from the subducted slab (basalts and sediments). HAM have constant IMITER ( e.g.Nb/U, Zr/K), whereas LAM show a negative correlation between IMITER and 87Sr /86Sr . Metasomatism of the mantle wedge was modelled by interaction with either a slab-derived-melt or -aqueous fluid. Yb/Sr and 87Sr /86Sr ratios from Slamet basalts and oceanic sediments suggest that 'bulk' mixing of the latter into the mantle wedge is unlikely. Instead, sediments probably interact with overlying mantle in the same way that subducted basalts do-either as melts or fluids. In the case of slab-derived melts mixing with 'pristine' mantle, good agreement with back-calculated values for HAM and LAM sources can be achieved only if a residual phase such as rutile persists in the subducting lithosphere. In the case of fluids, excellent agreement with back-calculated values is obtained for all elements except heavy REE. It is tentatively suggested that aqueous slab

  14. A high 87Sr 86Sr mantle source for low alkali tholeiite, northern Great Basin

    USGS Publications Warehouse

    Mark, R.K.; Lee, Hu C.; Bowman, H.R.; Asaro, F.; McKee, E.H.; Coats, R.R.

    1975-01-01

    Olivine tholeiites, the youngest Tertiary units (about 8-11 m.y. old) at five widely spaced localities in northeastern Nevada, are geologically related to the basalts of the Snake River Plain, Idaho, to the north and are similar in major element and alkali chemistry to mid-ocean ridge basalts (MORB) and island arc tholeiites. The measured K (1250-3350 ppm), Rb (1??9-6??2 ppm) and Sr (140-240 ppm) concentrations overlap the range reported for MORB. Three of the five samples have low, unfractionated rare earth element (REE) patterns, the other two show moderate light-REE enrichment. Barium concentration is high and variable (100-780 ppm) and does not correlate with the other LIL elements. The rocks have 87Sr/86Sr = 0??7052-0??7076, considerably higher than MORB (~0??702-0??703). These samples are chemically distinct (i.e. less alkalic) from the olivine tholeiites from the adjacent Snake River Plain, but their Sr isotopic compositions are similar. They contain Sr that is distinctly more radiogenic than the basalts from the adjacent Great Basin. About 10 b.y. would be required for the mean measured Rb/Sr (~ 0??02) of these samples to generate, in a closed system, the radiogenic Sr they contain. The low alkali content of these basalts makes crustal contamination an unlikely mechanism. If the magma is uncontaminated, the time-averaged Rb/Sr of the source material must have been ~0??04. A significant decrease in Rb/Sr of the source material (a factor 2??) thus most probably occurred in the relatively recent (1??09 yr) past. Such a decrease of Rb/Sr in the mantle could accompany alkali depletion produced by an episode of partial melting and magma extraction. In contrast, low 87Sr 86Sr ratios indicate that the source material of the mid-ocean ridge basalts may have been depleted early in the Earth's history. ?? 1975.

  15. 87Sr/86Sr Ratios in Carbonate From the Red Lake and Steep Rock Groups in Canada Suggest Rb-enriched Continental Crust was Influencing Seawater Chemistry Prior to 3.0 Ga

    NASA Astrophysics Data System (ADS)

    Satkoski, A.; Fralick, P. W.; Beard, B. L.; Johnson, C.

    2015-12-01

    Previous work has suggested that prior to 2.5 Ga, Sr isotope compositions of seawater were essentially mantle buffered and the effects of continental weathering on seawater chemistry were negligible. To test this, we collected Sr isotope data from 2.93 and 2.80 Ga carbonates that are part of the Red Lake and Steep Rock groups (Canada), respectively. To better understand carbonate formation and any post-depositional alteration, Sr isotopes are considered with O isotopes and REEs, as well as Rb and Sr contents, including correction for decay of 87Rb. All samples have Y/Ho ratios higher than chondrite and have positive La anomalies, which, combined with low Rb contents suggests that clastic contamination is negligible. Samples we consider near pristine have δ18O (VSMOW) values >20‰. Samples with the highest Y/Ho ratios and largest La anomalies from Red Lake and Steep Rock have initial 87Sr/86Sr ratios of 0.7018-0.7020. This Sr isotope composition is significantly more radiogenic than contemporaneous mantle (0.7011-0.7012), especially at a time when the isotopic difference between the crust and mantle was much less than today. This implies that radiogenic continental crust was emergent and shed detritus into the world's oceans prior to 3.0 Ga, in contrast with proposals for submerged continental crust, but in line with new estimates that continental crust at 3.0 Ga was 60-70% of current volume. We contend that this large amount of crust combined with enhanced Archean weathering could account for the radiogenic Sr isotope compositions we report here, and suggests a significant impact from continental weathering on ocean chemistry during the Archean.

  16. Ge/Si and 87Sr/86Sr tracers of weathering reactions and hydrologic pathways in a tropical granitoid system

    USGS Publications Warehouse

    Derry, L.A.; Pett-Ridge, J. C.; Kurtz, A.C.; Troester, J.W.

    2006-01-01

    Ge/Si and 87Sr/86Sr data from primary and secondary minerals, soil waters, and stream waters in a tropical granitoid catchment quantitatively reflect mineral alteration reactions that occur at different levels within the bedrock-saprolite-soil zone. Near the bedrock-saprolite interface, plagioclase to kaolinite reaction yields low Ge/Si and 87Sr/86Sr. Higher in the regolith column, biotite weathering and kaolinite dissolution drive Ge/Si and 87Sr/86Sr to high values. Data from streams at base flow sample the bedrock-saprolite interface zone, while at high discharge solutes are derived from upper saprolite-soil zone. Coupled Ge/Si and 87Sr/86Sr can be effective tools for quantifying the importance of specific weathering reactions, and for geochemical hydrograph separation. ?? 2005 Elsevier B.V. All rights reserved.

  17. The (87)Sr/(86)Sr strontium isotopic systematics applied to Glera vineyards: a tracer for the geographical origin of the Prosecco.

    PubMed

    Petrini, R; Sansone, L; Slejko, F F; Buccianti, A; Marcuzzo, P; Tomasi, D

    2015-03-01

    Glera vineyards from the Prosecco wine district in northern Italy have been characterised in terms of the (87)Sr/(86)Sr isotope-ratio of musts from the 2010, 2011 and 2012 vintages, coupled with the isotopic analysis of Sr in the labile fraction of the soils of provenance. For a single vineyard, detailed Sr isotopic analyses were carried out in sequentially extracted soil fractions at three different depths, and in the grape components (skin, seeds, must and stem), in order to verify the lack of Sr isotopic fractionation within the plant. The (87)Sr/(86)Sr in must, seeds and stem overlaps within experimental uncertainties; skins are shifted towards a lower Sr isotopic composition. A large range of Sr isotopic compositions ((87)Sr/(86)Sr between 0.70706 and 0.71215) characterizes musts from the different vineyards, notwithstanding the relatively limited extension of the investigated geographic area. A statistically significant correspondence between the soil labile fraction and must is observed.

  18. The evolution of oceanic 87Sr/86Sr does not rule out early continental growth

    NASA Astrophysics Data System (ADS)

    Flament, N.; Coltice, N.; Rey, P. F.

    2010-12-01

    Many contrasted continental growth models have been proposed to date, in which the amount of continental material extracted from the mantle at 3.8 Ga ranges between 0% (e.g. Taylor and McLennan, 1985) and 100% (e.g. Armstrong, 1981). One of the arguments in favor of delayed continental growth models is the shift in the 87Sr/86Sr of marine carbonates from mantle composition at ~ 2.8 Ga (Shields and Veizer, 2002). When using oceanic 87Sr/86Sr as a proxy of continental growth, the flux of strontium from the continents to the oceans is assumed to depend only on continental area and both continental hypsometry and continental freeboard are assumed to be constant through time. However, Rey and Coltice (2008) suggested that Archean reliefs were lower than present-day ones and Flament et al. (2008) suggested that the emerged land area is not proportional to continental growth. Therefore, the suitability of 87Sr/86Sr as a proxy of continental growth must be re-assessed. In this contribution, we develop an integrated model, from the mantle to the surface, to investigate the effect of contrasted continental growth models on the evolution of sea level, of the area of emerged land, and of oceanic 87Sr/86Sr. We estimate the evolution of mantle temperature using the model of Labrosse and Jaupart (2007) that takes the effect of continental growth into account. The maximum continental elevation is calculated using the results of Rey and Coltice (2008), sea level and the area of emerged land are calculated as in Flament et al. (2008), and the oceanic 87Sr/86Sr is calculated in a geochemical box model. We calculate Archean sea levels ~ 800 m higher than present for delayed continental growth and ~ 1500 m higher for early continental growth. In contrast, we calculate similar Archean areas of emerged land, of less than 5% of the Earth’s surface, for both early and delayed continental growth models. Because the area of emerged land does not depend on continental growth models, the

  19. 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.

  20. 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

  1. 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.

  2. Geochemical tracing of As pollution in the Orbiel Valley (southern France): 87Sr/86Sr as a tracer of the anthropogenic arsenic in surface and groundwater.

    NASA Astrophysics Data System (ADS)

    Khaska, Mahmoud; Le Gal La Salle, Corinnne; Lancelot, Joël; Verdoux, Patrick; Boutin, René

    2014-05-01

    The environmental impacts of arsenic mining activities and their effects on ecosystem and human health are observed in many stream waters and groundwater. The aim of this study is to identify the origin of As content in a mining environment using Sr isotopes. At the Salsigne gold mine, before the closure in 2004, high arsenic content has been observed in surface water and groundwater in the Orbiel valley. At the site, immobilization of As, in As rich leachate, is carried out by adding CaO. High contrast in 87Sr/86Sr between Arsenic rich minerals associated with Variscan metamorphic rocks (0.714888-0.718835), together with rich As waste water (0.713463-715477), and the CaO (0.707593) allows as to trace the origin of anthropogenic As. In 2012, Orbiel stream waters were sampled monthly upstream and downstream from the ancient ore processing site and once after an important rainy event (117mm). The upstream valley samples showed low and relatively constant As content with natural regional background of 3.6 and 5.6 μg/L. The rainy event induced only a slight increase in the As content up to 6.3 μg/L. High 87Sr/86Sr ratios suggested an influence of radiogenic Sr issued from the Variscan metamorphic basement. Downstream from the area, the As content was at least10 time as high. In the wet season, stream water As content clearly increased to 13.9-24 μg/L, reaching 120.5 μg/L during the rainy event. Associated 87Sr/86Sr ratio showed to be less radiogenic (0.712276-0.714002). The anti correlation observed between As and 87Sr/86Sr suggest that As issued from a natural origin is characterised by a high 87Sr/86Sr compared to As derived from the CaO treatement used on site and characterized by a low 87Sr/86Sr ratio. During the dry season, increase in As content was observed reaching 110 μg/L. These highlights the contribution of alluvial groundwater to base flow, probably associated with As reach leachate from the site. Contribution from the alluvial aquifer is confirmed by

  3. 44/40Ca and 87Sr/86Sr isotopes as tracers of silicate weathering in small catchments of the Massif Central, France

    NASA Astrophysics Data System (ADS)

    Négrel, Philippe; Guerrot, Catherine; Millot, Romain; Petelet-Giraud, Emmanuelle; Bullen, Thomas

    2013-04-01

    We present calcium stable isotope and strontium radiogenic isotope data for soils and sediments developed on volcanic and igneous rocks forming small catchments in the Massif Central (France). Measurements of 44/40Ca isotope ratios (44/40Ca measured by the double spike method on TIMS and normalized to the value for seawater Ca in delta units) in rocks, sediments and soils from silicate catchments (e.g. granite and basalts) together with 87Sr/86Sr isotope ratios permit an examination of the relationships of these isotope systematics during weathering of silicate rocks. We have analysed the granite, weathered granite (arene) and saprolite, sediment and soil overlying the granite on one hand and the basanite, sediment and soil overlying the basanite on the other. The main bedrock in the volcanic zone (e.g. Allanche catchment) is 11 to 2.5 Ma basanite (nephelinitic to leucitic basalts) having SiO2 between 41-45 wt. %, Na2O + K2O <5%, modal or normative nepheline or leucite and a ground mass of clinopyroxene and plagioclase. Surrounding rocks are feldspathic basalts having SiO2 between 46-49 wt. %, Na2O + K2O <5%, normative nepheline, hyperstene and olivine, with plagioclase as the main crystalline phase. The granite massif (e.g. Margeride, 332 ± 12Ma) consists of light and dark facies as a result of the fractional crystallisation of a crustal magma in a sub-horizontal laccolith, with leucogranites dated at 298±2 Ma intruding this granite. The average mineral composition is 37% quartz, 30% oligoclase, 23% K-feldspar and 10% biotite (light facies) and 31% quartz, 30% andesine, 20% K-feldspar and 19% biotite (dark facies). Sr isotope ratios in the arene, sediment and soil diverge strongly from those in the granite bedrock and are positively correlated with Rb/Sr ratios. The 87Sr/86Sr and Rb/Sr ratios both increase from the whole rock to the arene, reflecting the weathering of low 87Sr/86Sr, low-Rb/Sr minerals such as plagioclase and apatite. Sediments collected on a

  4. Combined marine δ88/86Sr and 87Sr/86Sr record supports global anoxia as a cause for P/T mass extinction

    NASA Astrophysics Data System (ADS)

    Vollstaedt, H.; Eisenhauer, A.; Boehm, F.; Fietzke, J.; Krabbenhöft, A.; Liebetrau, V.; Wallmann, K. J.; Farkas, J.

    2011-12-01

    The biggest mass extinction within the Phanerozoic Eon occurred at the Permian/Triassic (P/T) boundary and is characterized by up to 96% loss in species accompanied with the demise of the Paleozoic faunal community. Recently, five major mechanisms are consulted to explain the mass extinction in terrestrial and marine environment. However, a geochemical quantification of carbonate burial rates during this biotic turnover is still remaining. By extending the conventional radiogenic isotope system by a simultaneous measurement of radiogenic and stable strontium (Sr) isotopes (δ88/86Sr) we are able to add new constraints to the seawater chemistry including quantitative information about the Sr output flux of the ocean, mainly represented by marine carbonates. Consequently, variations in δ88/86Sr becoming a suitable tool to investigate in the global carbonate budget in earth's history including the biotic turnover of calcifying organisms at stratigraphic boundaries which are expected to have a large influence on Sr geochemistry and isotope composition of seawater. In order to examine variations in the marine Sr isotope composition through Earth's history paired 88Sr/86Sr-87Sr/86Sr-ratios of 104 Phanerozoic brachiopods, belemnites and carbonate matrix samples are determined. Applying the fractionation factor of our carbonate recording phase we constructed a δ88/86Srseawater record. The most noteworthy observation is the occurrence of the two global extrema in δ88/86Sr values of the whole Phanerozoic within the last 20Ma years of the Paleozoic prior to the P/T boundary. This corresponds to an increase of δ88/86Srseawater of 0.000249 Ma-1 in the latest Permian indicating a strong disturbance in the Sr budget of the ocean. To interpret our observations and to compare them to existing scenarios for the P/T boundary we applied a one-box, isotope mass balance model of the oceanic Sr cycle connected to a mass balance model of Ca. Our results show a high strontium output

  5. The major ion, 87Sr/86Sr, and δ11B geochemistry of groundwater in the Wyodak-Anderson coal bed aquifer (Powder River Basin, Wyoming, USA)

    NASA Astrophysics Data System (ADS)

    Lemarchand, Damien; Jacobson, Andrew D.; Cividini, Damien; Chabaux, François

    2015-11-01

    We developed a multicomponent, 1D advective transport model that describes the downgradient evolution of solute concentrations, 87Sr/86Sr ratios, and δ11B values in the Wyodak-Anderson Coal Bed (WACB) aquifer located in the Powder River Basin, Wyoming, USA. The purpose of the study was to evaluate the chemical vulnerability of groundwater to potential environmental change stemming from the extraction of coal bed methane and shale gas. Model calculations demonstrate that coupling between microbial activity and the dissolved carbonate system controls major ion transport in the WACB aquifer. The analysis of 87Sr/86Sr ratios further reveals the importance of ion-exchange reactions. Similarly, δ11B data emphasize the significance of pH-dependent surface reactions and demonstrate the vulnerability of the aquifer to the long-term acidification of recharge water.

  6. The sup 87 Sr/ sup 86 Sr values of Canadian Shield brines and fracture minerals with applications to groundwater mixing, fracture history, and geochronology

    SciTech Connect

    McNutt, R.H. ); Frape, S.K.; Fritz, P.; Jones, M.G.; MacDonald, I.M. )

    1990-01-01

    Analyses of saline waters, fracture minerals, and host rocks from seven localities on the Canadian Shield demonstrate the utility of the {sup 87}Sr/{sup 86}Sr ratio in the study of groundwater systems in crystalline rocks. The ratios range from 0.704 to 0.753 and have obtained their signatures by mineral/rock interactions, primarily involving the feldspars. The authors have identified brines from isolated pockets in the same mines where extensive flow regimes exist. There is a mixing of different brines as well as mixing with meteoric waters. The isotopic results on calcites from fractures and shear zones show more than one generation of mineral growth in a given fracture. The {sup 87}Sr/{sup 86}Sr ratios of the calcites vary from values identical to the present-day brine in the fracture zone to ratios with Archean signatures. This implies that activity may occur in fault zones over a very long time. The brines are very rich in Sr (up to 2400 mg/l), very low in Rb, and have relatively radiogenic {sup 87}Sr/{sup 86}Sr ratios. They are ubiquitous in Shield rocks and, if they were present throughout geological time, they may be one reason why Rb/Sr ages of felsic plutons are commonly younger than associated U/Pb ages.

  7. Analysis of coupled Sr/Ca and 87Sr/ 86Sr variations in enamel using laser-ablation tandem quadrupole-multicollector ICPMS

    NASA Astrophysics Data System (ADS)

    Balter, Vincent; Telouk, Philippe; Reynard, Bruno; Braga, José; Thackeray, Francis; Albarède, Francis

    2008-08-01

    We present in this study results obtained with a laser-ablation coupled with both a quadrupole and a multi-collector ICPMS. The simultaneous in situ Sr/Ca and 87Sr/ 86Sr measurements along growth profiles in enamel allows the concomitant diet and migration patterns in mammals to be reconstructed. Aliquots of the powdered international standard NIST "SRM1400 Bone Ash" with certified Sr and Ca contents, was sintered at high pressure and temperature and was adopted as the reference material for external reproducibility and calibration of the results. A total of 145 coupled elemental and isotopic measurements of herbivores enamel from the Kruger National Park, South Africa, gives intra-tooth Sr/Ca and 87Sr/ 86Sr variations that are well larger than external reproducibility. Sr/Ca profiles systematically decrease from the dentine-enamel junction to the outer enamel whereas 87Sr/ 86Sr profiles exhibit variable patterns. Using a simple geometric model of hypsodont teeth growth, we demonstrate that a continuous recording of the 87Sr/ 86Sr variations can be reconstructed in the tooth length axis. This suggests that the mobility of a mammal can be reconstructed over a period of more than a year with a resolution of a ten of days, by sampling enamel along growth profiles. Our geometric model of hypsodont teeth growth predicts that an optimal distance between two successive profiles is equal to the enamel thickness. However, this model does not apply to the Sr/Ca signal which is likely to be altered during the enamel maturation stage due to differential maturation processes along enamel thickness. Here, the observed constant decreases of the Sr/Ca ratios in the ungulates of Kruger National Park suggests that they did not changed of diet, while some of them were migrating.

  8. The (87)Sr/(86)Sr strontium isotopic systematics applied to Glera vineyards: a tracer for the geographical origin of the Prosecco.

    PubMed

    Petrini, R; Sansone, L; Slejko, F F; Buccianti, A; Marcuzzo, P; Tomasi, D

    2015-03-01

    Glera vineyards from the Prosecco wine district in northern Italy have been characterised in terms of the (87)Sr/(86)Sr isotope-ratio of musts from the 2010, 2011 and 2012 vintages, coupled with the isotopic analysis of Sr in the labile fraction of the soils of provenance. For a single vineyard, detailed Sr isotopic analyses were carried out in sequentially extracted soil fractions at three different depths, and in the grape components (skin, seeds, must and stem), in order to verify the lack of Sr isotopic fractionation within the plant. The (87)Sr/(86)Sr in must, seeds and stem overlaps within experimental uncertainties; skins are shifted towards a lower Sr isotopic composition. A large range of Sr isotopic compositions ((87)Sr/(86)Sr between 0.70706 and 0.71215) characterizes musts from the different vineyards, notwithstanding the relatively limited extension of the investigated geographic area. A statistically significant correspondence between the soil labile fraction and must is observed. PMID:25306328

  9. Use of 87Sr/86Sr and delta11B to identify slag-affected sediment in southern Lake Michigan.

    PubMed

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

    2004-03-01

    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 deltat11B. 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 delta11B values occurred in sediments from the Indiana shoreline (+12.9 to 16.4/1000) but were also elevated in sediments collected offshore from three Lake Michigan cities (+11.7 to 12.7/1000). Contoured isotope data indicated that 82-154 km2 of bed sediment along the Indiana shoreline had elevated 87Sr/86Sr and delta11B values relative to shoreline sediments elsewhere in southern Lake Michigan.

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

    USGS Publications Warehouse

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

    2004-01-01

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

  11. 87Sr/86Sr in recent accumulations of calcium sulfate on landscapes of hyperarid settings: A bimodal altitudinal dependence for northern Chile (19.5°S-21.5°S)

    NASA Astrophysics Data System (ADS)

    Cosentino, N. J.; Jordan, T. E.; Derry, L. A.; Morgan, J. P.

    2015-12-01

    An elevation-dependent relationship of the 87Sr/86Sr ratio of Holocene surface accumulations of sulfate salts is demonstrated for a continental margin hyperarid setting. In the Atacama Desert of northern Chile, gypsum and anhydrite of multiple origins exist widely on superficial materials that originated during the last 10,000 years. An important source of calcium sulfate is from offshore-generated stratocumulus clouds that are advected onto the continent, where they generate fog that transfers water droplets to the ground surface which, upon evaporation, leaves calcium sulfate crystals. Meteorological measurements of the cloud base and top altitudes average ˜400 m and ˜1100 m above sea level (masl), respectively. The seawater ratio of 87Sr/86Sr (0.70917) is distinctively higher than that reported for weathered mean Andean rock (less than 0.70750). Samples of 28 modern surface salt accumulations for locations between 200 and 2950 masl and between ˜19°30' and ˜21°30'S verify that 87Sr/86Sr varies as a function of site altitude. Sites below 1075 masl and above 225 masl display calcium sulfate 87Sr/86Sr of mean value 0.70807 ± 0.00004, while the ratio outside this altitudinal domain is 0.70746 ± 0.00010. Thus, the 87Sr/86Sr ratio of Holocene salt accumulations differentiates two altitudinal domains.

  12. Magnetic susceptibility and relation to initial 87Sr/86Sr for granitoids of the central Sierra Nevada, California

    USGS Publications Warehouse

    Bateman, P.C.; Dodge, F.C.W.; Kistler, R.W.

    1991-01-01

    Measurement of the magnetic susceptibility of more than 6000 samples of granitic rock from the Mariposa 1?? by 2?? quadrangle, which crosses the central part of the Sierra Nevada batholith between 37?? and 38??N latitude, shows that magnetic susceptibility values are above 10-2 SI units in the east and central parts of the batholith and drop abruptly to less than 10-3 SI units in the western foothills. In a narrow transitional zone, intermediate values (10-3 to 10-2) prevail. Magnetic susceptibility appears to decrease slightly westward within the zones of both high and low values. Magnetic susceptibility in plutonic rocks is chiefly a function of the abundance of magnetite, which depends, in turn, on the total iron content of the rocks and their oxidation ratio. Correlations of magnetic susceptibility with initial 87Sr/86Sr suggest that oxidation ratios have been inherited from the source regions for the magmas from which the rocks crystallized. Reduction of Fe3+ to Fe2+ by organic carbon or other reducing substances may also have affected magnetic susceptibility. -from Authors

  13. 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.

  14. Strontium isotope (87Sr/86Sr) variability in the Nile Valley: identifying residential mobility during ancient Egyptian and Nubian sociopolitical changes in the New Kingdom and Napatan periods.

    PubMed

    Buzon, Michele R; Simonetti, Antonio

    2013-05-01

    As a successful technique for identifying residential mobility in other areas, this study investigates the feasibility of using 87Sr/86Sr analysis to track the movements of the ancient peoples of Egypt and Nubia in the Nile Valley, who interacted via trade, warfare, and political occupations over millennia. Dental enamel from faunal remains is used to examine variability in strontium sources in seven regional sites; human enamel samples are analyzed from eight Nile Valley sites in order to trace human movements. The faunal samples show a wide range of 87Sr/86Sr values demonstrating that some animals were raised in a variety of locales. The results of the human samples reveal overlap in 87Sr/86Sr values between Egyptian and Nubian sites; however, Egyptian 87Sr/86Sr values (mean/median [0.70777], sd [0.00027]) are statistically higher than the Nubian 87Sr/86Sr values (mean [0.70762], median [0.70757], sd [0.00036], suggesting that it is possible to identify if immigrant Egyptians were present at Nubian sites. Samples examined from the site of Tombos provide important information regarding the sociopolitical activities during the New Kingdom and Napatan periods. Based on a newly established local 87Sr/86Sr range, human values, and bioarchaeological evidence, this study confirms the preliminary idea that immigrants, likely from Egypt, were present during the Egyptian New Kingdom occupation of Nubia. In the subsequent Napatan period when Nubia ruled Egypt as the 25th Dynasty, 87Sr/86Sr values are statistically different from the New Kingdom component and indicate that only locals were present at Tombos during this developmental time.

  15. Major-ion chemistry, δ13C and 87Sr/86Sr as indicators of hydrochemical evolution and sources of salinity in groundwater in the Yuncheng Basin, China

    NASA Astrophysics Data System (ADS)

    Currell, Matthew J.; Cartwright, Ian

    2011-06-01

    Processes controlling hydrogeochemistry in the Yuncheng Basin, China, were characterised using major-ion chemistry, 87Sr/86Sr ratios and δ13C values. Evapotranspiration during recharge increased solute concentrations by factors of ˜5-50 in deep palaeowaters, while higher degrees of evapotranspiration have occurred in shallow, modern groundwater. Aquifer sediments (loess) contain approximately 15 weight% calcite; trends in groundwater HCO3 concentrations and δ13C values (ranging from -16.4 to -8.2‰) indicate that carbonate weathering is a significant source of DIC. Groundwater 87Sr/86Sr ratios (0.7110-0.7162, median of 0.7116) are similar to those in both loess carbonate (0.7109-0.7116) and local rainfall (0.7112), and are significantly lower than Sr in aquifer silicates (0.7184-0.7251). Despite evidence for substantial carbonate dissolution, groundwater is generally Ca-poor (< 10% of total cations) and Na-rich, due to cation exchange. Saturation with respect to carbonate minerals occurs during or soon after recharge (all calcite and dolomite saturation indices are positive). Subsequent carbonate dissolution in the deep aquifer must occur as a second-stage process, in response to Ca loss (by ion exchange) and/or via incongruent dissolution of dolomite and impure calcite. The latter is consistent with positive correlations between δ13C values and Mg/Ca and Sr/Ca ratios ( r 2 = 0.32 and 0.34).

  16. 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, G. 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

  17. 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.

  18. 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. PMID:25789981

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

    PubMed

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

    2015-07-21

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

  20. Sr and 87Sr/ 86Sr in the Yamuna River System in the Himalaya: sources, fluxes, and controls on sr isotope composition

    NASA Astrophysics Data System (ADS)

    Dalai, Tarun K.; Krishnaswami, S.; Kumar, Anil

    2003-08-01

    Sr and 87Sr/ 86Sr have been measured in the Yamuna river headwaters and many of its tributaries (YRS) in the Himalaya. These results, with those available for major ions in YRS rivers and in various lithologies of their basin, have been used to determine their contributions to riverine Sr and its isotopic budget. Sr in the YRS ranges from 120 to 13,400 nM, and 87Sr/ 86Sr from 0.7142 to 0.7932. Streams in the upper reaches, draining predominantly silicates, have low Sr and high 87Sr/ 86Sr whereas those draining the lower reaches exhibit the opposite resulting from differences in drainage lithology. 87Sr/ 86Sr shows significant co-variation with SiO 2/TDS and (Na * + K)/TZ + (indices of silicate weathering) in YRS waters, suggesting the dominant role of silicate weathering in contributing to high radiogenic Sr. This is also consistent with the observation that streams draining largely silicate terrains have the highest 87Sr/ 86Sr, analogous to that reported for the Ganga headwaters. Evaluation of the significance of other sources such as calc-silicates and trace calcites in regulating Sr budget of these rivers and their high 87Sr/ 86Sr needs detailed work on their Sr and 87Sr/ 86Sr. Preliminary calculations, however, indicate that they can be a significant source to some of the rivers. It is estimated that on an average, ˜25% of Sr in the YRS is derived from silicate weathering. In the lower reaches, the streams receive ˜15% of their Sr from carbonate weathering whereas in the upper reaches, calc-silicates can contribute significantly (˜50%) to the Sr budget of rivers. These calculations reveal the need for additional sources for rivers in the lower reaches to balance their Sr budget. Evaporites and phosphorites are potential candidates as judged from their occurrence in the drainage basin. In general, Precambrian carbonates, evaporites, and phosphorites "dilute" the high 87Sr/ 86Sr supplied by silicates, thus making Sr isotope distribution in YRS an overall two

  1. Authentication potential of 87Sr/86Sr in water - reference of signatures in natural mineral water to regional geology in Europe

    NASA Astrophysics Data System (ADS)

    Lorenz, G. D.; Voerkelius, S.

    2009-04-01

    The study presents the investigation of strontium isotope ratios of about 650 different European natural mineral waters as part of the food traceability project "TRACE" funded by the EU. The 87Sr/86Sr analysis is part of a multi-element approach for authen-ticity which also includes 18O, 2H, 3H, main and trace elements as well as 34S. The analysed 87Sr/86Sr cover a wide range of values from 0.7035 to 0.7777 indicating that the natural mineral water samples cover the span from young mantle derived basal-tic rocks to very old silicic continental crust. The results of the large-scale investigation are used to elaborate a novel spatial predic-tion for strontium isotope ratios by combining the measured data with a GIS based geo-logical map of Europe. The resulting map can be used to predict the strontium isotopic composition of ground-water and as such the composition of bioavailable strontium, which can be taken up by plants and further transferred into the food chain. In this study we show, as an example, that the strontium isotopic composition of honey and wheat from specific sample region within the TRACE project correlates well with that of the natural mineral water as pre-dicted by our map. The proof of principle shown is highly relevant for geographical food authentication as it will allow an assessment of the origin of food products without the immediate need for geographically authenticated materials which may not always be available in the first instance. As such, our approach provides a cost effective first instance screening tool. There is an increasing demand for independent analytical methods which can control the geographical origin. The EU project TRACE was started with the aim to develop a gen-eral understanding of the relation between the geo-bio-climatic environment and the isotope and elemental signature in food commodities. As one part of the study detailed isotope maps (e.g. 18O, 87Sr/86Sr) for groundwater will be generated by the isotope re

  2. High-latitude application of sup 87 Sr/ sup 86 Sr: Correlation of Nuwok beds on North Slope, Alaska, to standard Oligocene chronostratigraphy

    SciTech Connect

    McNiel, D.H. ); Miller, K.G. )

    1990-05-01

    Strontium isotope ratios ({sup 87}Sr/{sup 86}Sr) calculated from three samples of benthic forminifers and one mallusc indicate an age range from 23.8 to 27.0 Ma for the Nuwok Member of the Sagavanirktok Formation, eastern North Slope, Alaska. Previous correlations derived paleontologically (foraminifers, ostracodes, and molluscs) for the Nuwok beds have differed greatly (Oligocene to Pliocene), but strontium isotope ratios substantiate the late Oligocene age determined from benthic foraminifers. The results constitute an important test case, illustrating the effectiveness of the strontium isotope method in correlating high-latitude carbonate samples to the standard Oligocene chronostratigraphy. In addition, a sample from the Kugmallit sequence in the Beaufort Sea Edlok N-56 well provided a strontium isotope age estimate of 30.7 Ma. The Edlok sample was paleontologically correlated to just below the early/late Oligocene boundary (30.0 Ma).

  3. Constraining water balance in the Bonneville Basin during the last glacial period and deglaciation using 87Sr/86Sr and δ18O of lacustrine carbonates

    NASA Astrophysics Data System (ADS)

    Steponaitis, E.; McGee, D.; Quade, J.; Edwards, R.; Broecker, W. S.; Cheng, H.; Reiners, P. W.; Evenson, N. S.

    2012-12-01

    Geochemical records from closed basin lakes provide important constraints on past changes in regional precipitation - evaporation (P-E). This study refines our understanding of paleohydrology in the Bonneville Basin and explores the Basin's response to past abrupt changes, including Heinrich Event 2. We present Sr and O isotope records from lacustrine carbonates deposited in caves and other protected spaces during periods of higher lake levels (McGee et al., 2012). These records, anchored by precise U/Th and 14C dating, offer new insights into changes in lake level and water balance during the last glacial period and deglaciation. The Sr isotope composition of lake water is determined by the relative contributions of the two major fluvial inputs to the lake, the Bear River in the north and the Sevier River in the south, which have distinct 87Sr/86Sr ratios (Hart et al. 2004). Sr ratios of lake water, as recorded in lacustrine carbonates from different locations and elevations in the basin, offer insight into both lake mixing and changes in the position of the winter storm track, the primary source of precipitation to the Great Basin. High-resolution δ18O data from the carbonates trace changes in basin P-E and water column mixing. Trace element concentrations in the carbonates, especially those of Mg, Rb and Ba, are used to test interpretations of Sr and O isotope changes. Hart, W.S. et al., The 87Sr/86Sr ratios of lacustrine carbonates and lake-level history of the Bonneville paleolake system. GSA Bulletin 2004; 116: 1107-1119. McGee, D., et al. Lacustrine cave carbonates: Novel archives of paleohydrologic change in the Bonneville Basin (Utah, USA). EPSL 2012; In press.

  4. Compilation and review of 87Sr/86Sr and stable isotopes from groundwater, calcite fracture fillings, mineral, and whole-rock sampling at Äspö, Sweden.

    PubMed

    Wallin, Bill; Peterman, Zell

    2015-04-01

    Integrated isotopic and hydrochemical studies of groundwater at Äspö, Sweden, support mixing models involving deep saline water, low-solute infiltration, and Baltic Sea water. Carbon, oxygen, and strontium isotope analyses of calcite fracture fillings indicate that paleohydrologic conditions were different than those of today in terms of the isotopic composition of water flowing through fractures. Sr isotopes of whole-rock and mineral (plagioclase, microcline, biotite, and epidote) samples are used to assess the effects of water-rock interaction. Biotite is a major reactant in the early stages of water-rock interaction. Strontium isotope systematics of groundwater from deep in the Hard Rock Laboratory, and underground research facility, and from low conductivity zones revealed a first order mixing line defined by a high-chloride saline component with 66 mg/L Sr and an ancient sea water component with approximately 4.5 mg/L. Dilution with low salinity recharge has produced groundwater with variable Sr contents and 87Sr/86Sr values between 0.7186 and 0.7160. Differences between Äspö and Laxemar groundwater are shown by trends in Sr concentrations plotted against 87Sr/86Sr. The Äspö trend shows increasing 87Sr/86Sr values with increasing concentrations of Sr, whereas the Laxemar groundwater trend shows little variability in 87Sr/86Sr with increasing Sr concentrations. These trends are controlled by the differences in 87Sr/86Sr composition of the saline end members in the two areas.

  5. Compilation and review of 87Sr/86Sr and stable isotopes from groundwater, calcite fracture fillings, mineral, and whole-rock sampling at Äspö, Sweden.

    PubMed

    Wallin, Bill; Peterman, Zell

    2015-04-01

    Integrated isotopic and hydrochemical studies of groundwater at Äspö, Sweden, support mixing models involving deep saline water, low-solute infiltration, and Baltic Sea water. Carbon, oxygen, and strontium isotope analyses of calcite fracture fillings indicate that paleohydrologic conditions were different than those of today in terms of the isotopic composition of water flowing through fractures. Sr isotopes of whole-rock and mineral (plagioclase, microcline, biotite, and epidote) samples are used to assess the effects of water-rock interaction. Biotite is a major reactant in the early stages of water-rock interaction. Strontium isotope systematics of groundwater from deep in the Hard Rock Laboratory, and underground research facility, and from low conductivity zones revealed a first order mixing line defined by a high-chloride saline component with 66 mg/L Sr and an ancient sea water component with approximately 4.5 mg/L. Dilution with low salinity recharge has produced groundwater with variable Sr contents and 87Sr/86Sr values between 0.7186 and 0.7160. Differences between Äspö and Laxemar groundwater are shown by trends in Sr concentrations plotted against 87Sr/86Sr. The Äspö trend shows increasing 87Sr/86Sr values with increasing concentrations of Sr, whereas the Laxemar groundwater trend shows little variability in 87Sr/86Sr with increasing Sr concentrations. These trends are controlled by the differences in 87Sr/86Sr composition of the saline end members in the two areas. PMID:24571642

  6. Permian Minimum and the Following Major Rise in Seawater 87Sr/86Sr Linked to the Glaciation/Deglaciation and Resultant Change in Weathering Rate

    NASA Astrophysics Data System (ADS)

    Kani, T.; Isozaki, Y.

    2014-12-01

    We report a detailed secular change of the middle Middle to early Late Permian seawater 87Sr/86Sr ratio for and Akasaka and Kamura carbonates (Japan) deposited on mid-Pansalassan seamounts and for Shizipo carbonates (South China) deposited on the shallow marine shelf. In these coeval sections, extremely low values (<0.7069; the lowest values of the Phanerozoic) continued from upper Wordian (middle Middle Permian) to the topmost Capitanian (upper Middle Permian) barren interval immediately below the Middle-Late Permian boundary characterized by the major crisis of large-tested fusulines and rugose corals. Immediately after ca. 5 m.y.-long minimum interval, the major rise in 87Sr/86Sr was started and the rate of the rise (0.00007/m.y.) continued in period of time containing 21 m.y. until early Triassic (~239 Ma), that is faster than the Cenozoic major rise (0.00003/m.y.). The most significant shift through Phanerozoic in Sr isotope trend can be explained by the remarkable changes in continental erosion/weathering rate; in particular, by the onset of glaciation and the following deglaciation, that is supported by global sea level change, in addition to the initial doming/rifting of Pangea. After the Capitanian cooling, the long-term climatic regime shifted to a warmer one during which inland ice sheet was removed to expose old crustal silicates for to erosion/weathering. A mantle plume impingiment might lead a domal uplift that accelerate weathering. Highly radiogenic continental Sr could enter the ocean along the new drainage systems developed with the rifting.

  7. 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

  8. 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

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

    SciTech Connect

    Podosek, F.A.; Zinner, E.K.; Lundeberg, L.L.; Brannon, J.C.; Fahey, A.J. ); MacPherson, G.J. )

    1991-04-01

    The authors have studied a suite of six coarse-grained Ca-Al-rich inclusions (CAIs) from the Allende meteorite, applying in concert detailed petrographic and chemical characterization, ion probe mass spectrometric analyses of the Al-Mg isotopic system to determine the abundance and distribution of {sup 26}Al, and thermal emission mass spectrometric analyses of the Rb-Sr system to determine initial {sup 87}Sr/{sup 86}Sr ratios. The simplest inclusion is a Type B1, USNM 3529-Z, that shows evidence of minor alteration and recrystallization since solidification from a melt droplet. The Rb-Sr isotopic system also typically indicates some level of disturbance, some of which must have been relatively recent. Nevertheless, phases characterized by very low Rb/Sr permit precise identification of initial {sup 87}Sr/{sup 86}Sr. Our Al-Mg and Sr data are largely consistent with a simple chronological interpretation of both systems. The present data are the first which establish a firm association between primitive {sup 26}Al/{sup 27}Al and primitive {sup 87}Sr/{sup 86}Sr by analysis of both isotopic systems in the same inclusions. The comparison of both isotopic systems, interpreted as simple nebular chronometers, does not reveal any chronological inconsistencies that demand resolution in terms of a grossly heterogeneous distribution of {sup 26}Al.

  10. Geochemistry of Cambro-Ordovician Arbuckle limestone, Oklahoma: Implications for diagenetic. delta. sup 18 O alteration and secular. delta. sup 13 C and sup 87 Sr/ sup 86 Sr variation

    SciTech Connect

    Gao, Guoqiu; Land, L.S. )

    1991-10-01

    Isotopic analyses of 227 limestone samples from the Cambro-Ordovician Arbuckle Group, Oklahoma, document slow secular changes in the chemistry of the limestones. From late Cambrian to early Ordovician, the {delta}{sup 18}O values of the limestones increase from {minus}10{per thousand} to {minus}7{per thousand} (PDB); {delta}{sup 13}C values decrease from 0{per thousand} to {minus}2{per thousand} (PDB); and {sup 87}Sr/{sup 86}Sr ratios decrease from 0.7091 to 0.7088. The light {delta}{sup 18}O values suggest that all Arbuckle limestones underwent diagenetic alteration, probably caused by meteoric water recharged during the development of the overlying, pre-middle Ordovician unconformity. The gradual {delta}{sup 18}O increase from late Cambrian to early Ordovician reflects reduced {sup 18}O depletion with decreasing burial temperature during alteration, although the presence of additional primary secular {delta}{sup 18}O variation cannot be ruled out. The {delta}{sup 13}C and {sup 87}Sr/{sup 86}Sr variations, in accord with {delta}{sup 13}C and {sup 87}Sr/{sup 86}Sr variations in the literature, represent primary secular variations. The variations indicate that the {delta}{sup 13}C value and {sup 87}Sr/{sup 86}Sr ratio of early Paleozoic surface seawater decreased from late Cambrian to early Ordovician. The {delta}{sup 13}C variation during this time period seems to correlate with sea-level variation. Specifically, during sea-level fall, an increase in the rate of oxidation of organic matter caused {sup 13}C depletion of inorganic bicarbonate in seawater. As a result, early Ordovician carbonates, probably deposited during the regression stage of the latest Precambrian to latest early Ordovician cycle, became {sup 13}C depleted, relative to late Cambrian carbonates. The decrease of seawater {sup 87}Sr/{sup 86}Sr ratio from late Cambrian to early Ordovician may have resulted from decreased riverine Sr input caused by decreased rate of continental weathering.

  11. Patterns of Ca/Sr and 87Sr/ 86Sr variation before and after a whole watershed CaSiO 3 addition at the Hubbard Brook Experimental Forest, USA

    NASA Astrophysics Data System (ADS)

    Nezat, Carmen A.; Blum, Joel D.; Driscoll, Charles T.

    2010-06-01

    Forty-one metric tons of the mineral wollastonite (CaSiO 3) was applied to an 11.8 hectare watershed at the Hubbard Brook Experimental Forest (HBEF; White Mountains, New Hampshire, USA) with the goal of restoring the Ca estimated to have been depleted from the soil exchange complex by acid deposition. This experiment provided an opportunity to gain qualitative information on whole watershed hydrologic flow paths by studying the response of stream water chemistry to the addition of Ca. Because the Ca/Sr and 87Sr/ 86Sr ratios of wollastonite strongly contrast that of other Ca sources in the watershed, the wollastonite-derived Ca can be identified and its amount estimated in various ecosystem components. Stream water chemistry at the HBEF varies seasonally due to shifts in the proportion of base flow and interflow. Prior to the wollastonite application, seasonal variations in 87Sr/ 86Sr ratios indicated that 87Sr/ 86Sr was higher during base flow than interflow, due largely to greater amounts of biotite weathering along deeper flow paths. After the application, Ca/Sr and 87Sr/ 86Sr changed markedly as the high Ca/Sr and low 87Sr/ 86Sr wollastonite dissolved and mixed with stream water. The Ca addition provided information on the response times of various flow paths and ion exchange processes to Ca addition in this small upland watershed. During the first year after the addition, wollastonite applied to the near stream zone dissolved and was partially immobilized by cation exchange sites in the hyporheic zone. In the second and third years after the addition we infer that much of this Ca and Sr was subsequently desorbed from the hyporheic zone and was exported from the watershed in stream flow. In the fourth through ninth years after the addition, Ca and Sr from wollastonite that had dissolved in upland soils was transported to the stream by interflow during wet periods when the ground water table was elevated. Between years three and nine the minimum annual Ca

  12. 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

  13. 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

  14. 87Sr/86Sr as a quantitative geochemical proxy for 14C reservoir age in dynamic, brackish waters: Assessing applicability and quantifying uncertainties

    NASA Astrophysics Data System (ADS)

    Lougheed, Bryan C.; Lubbe, H. J. L.; Davies, Gareth R.

    2016-01-01

    Accurate geochronologies are crucial for reconstructing the sensitivity of brackish and estuarine environments to dynamic external impacts of the past. Radiocarbon (14C) dating is commonly used for palaeoclimate studies, 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. Additionally, old carbon effects and species-specific behavioral 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 (using GIS) and species-specific 14C effects, we demonstrate the use of 87Sr/86Sr ratios for quantifying R(t) in ubiquitous mollusc shell material, leading to almost an order of magnitude increase in Baltic Sea 14C geochronological precision over the current state of the art. We propose that similar proxy methods can be developed for other brackish water bodies worldwide.

  15. 87Sr/86Sr as a quantitative geochemical proxy for 14C reservoir age in dynamic, brackish waters: assessing applicability and quantifying uncertainties.

    NASA Astrophysics Data System (ADS)

    Lougheed, Bryan; van der Lubbe, Jeroen; Davies, Gareth

    2016-04-01

    Accurate geochronologies are crucial for reconstructing the sensitivity of brackish and estuarine environments to rapidly changing past 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. 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 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.

  16. Lower to middle Miocene isotope ( sup 87 Sr/ sup 86 Sr,. delta. sup 18 O,. delta. sup 13 C) standard sections, DSDP site 608

    SciTech Connect

    Miller, K.G.; Feigenson, M.D. ); Wright, J.D. )

    1990-05-01

    Isotopes changes ({sup 87}Sr/{sup 86}Sr, {delta}{sup 18}O, {delta}{sup 13}C) have been correlated to the geologic time scale primarily by biostratigraphy. Biostratigraphic correlations suffer from problems of diachrony and taxonomy. Magnetostratigraphy provides a facies-independent correlation tool, but there are few Tertiary sections with unambiguous magnetostratigraphy. The authors previously developed an isotope standard for the Oligocene at the only location with a pristine magnetochronology, Site 522. They extend this approach to Site 608 in the northeastern North Atlantic, which contains a relatively straightforward Miocene magnetochronology. They establish Miocene oxygen isotope Chronozones MI1 through MI6 at Sites 522 and 608, which are directly tied to the geomagnetic polarity time scale (GPTS). The integration of stable isotopes, Sr isotopes, biostratigraphy, and magnetostratigraphy at site 608 provides a standard section with which other Sr isotope and oxygen isotope records can be correlated. For example, using oxygen isotopes to correlate, the Sr isotope record from Site 608 compares well with previously published records from Sites 516 and 590. The firm ties of the Oligocene to middle Miocene isotope records with the GPTS allows them to establish the nature of the change in Sr isotopes between 38 and 8 Ma. There were moderately high rates of {sup 87}Sr/{sup 86}Sr change during the Oligocene ({approximately}0.000030/m.y.), yielding stratigraphic resolution of {plus minus}1.0 m.y. The rate of change of {sup 87}Sr/{sup 86}Sr increased during the early Miocene. They estimate that the rate of change between 23 and 15 Ma was greater than 0.000060/m.y. Given their ability to reproduce Sr isotope measurements ({plus minus}0.000020 to {plus minus}0.000030), temporal resolution is better than {plus minus}0.5 my. for the early to early middle Oliocene.

  17. 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

  18. Tracing thermal aquifers of El Chichón volcano-hydrothermal system (México) with 87Sr/ 86Sr, Ca/Sr and REE

    NASA Astrophysics Data System (ADS)

    Peiffer, L.; Taran, Y. A.; Lounejeva, E.; Solís-Pichardo, G.; Rouwet, D.; Bernard-Romero, R. A.

    2011-08-01

    The volcano-hydrothermal system of El Chichón volcano, Chiapas, Mexico, is characterized by numerous thermal manifestations including an acid lake, steam vents and boiling springs in the crater and acid and neutral hot springs and steaming ground on the flanks. Previous research on major element chemistry reveals that thermal waters of El Chichón can be divided in two groups: (1) neutral waters discharging in the crater and southern slopes of the volcano with chloride content ranging from 1500 to 2200 mg/l and (2) acid-to-neutral waters with Cl up to 12,000 mg/l discharging at the western slopes. Our work supports the concept that each group of waters is derived from a separate aquifer (Aq. 1 and Aq. 2). In this study we apply Sr isotopes, Ca/Sr ratios and REE abundances along with the major and trace element water chemistry in order to discriminate and characterize these two aquifers. Waters derived from Aq. 1 are characterized by 87Sr/ 86Sr ratios ranging from 0.70407 to 0.70419, while Sr concentrations range from 0.1 to 4 mg/l and Ca/Sr weight ratios from 90 to 180, close to average values for the erupted rocks. Waters derived from Aq. 2 have 87Sr/ 86Sr between 0.70531 and 0.70542, high Sr concentrations up to 80 mg/l, and Ca/Sr ratio of 17-28. Aquifer 1 is most probably shallow, composed of volcanic rocks and situated beneath the crater, within the volcano edifice. Aquifer 2 may be situated at greater depth in sedimentary rocks and by some way connected to the regional oil-gas field brines. The relative water output (l/s) from both aquifers can be estimated as Aq. 1/Aq. 2-30. Both aquifers are not distinguishable by their REE patterns. The total concentration of REE, however, strongly depends on the acidity. All neutral waters including high-salinity waters from Aq. 2 have very low total REE concentrations (< 0.6 μg/l) and are characterized by a depletion in LREE relative to El Chichón volcanic rock, while acid waters from the crater lake (Aq. 1) and acid

  19. 87Sr/86Sr in Gypsic Relict Soils and Paleosols of Hyperarid Settings as a Paleoaltitude Proxy: Results for Northern Chile (19.5-21.7°S)

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

    We have developed a new altimeter proxy based on the 87Sr/86Sr ratio of surficial accumulations of salts in hyperarid settings. Under hyperarid conditions like in the Andean forearc in northern Chile at altitudes below ~3000 m.a.s.l., gypsum and other soluble salts form saline soils. The altimeter is based on the first-order topographic control on the extent of inland incursion of fog-transported marine aerosols derived from the Pacific Ocean. Once this fog is evaporated it deposits calcium sulfates with a marine 87Sr/86Sr signal. At positions in the landscape not reached by marine aerosols, calcium sulfates have no marine source, except by eolian reworking, and have a lower 87Sr/86Sr. 87Sr/86Sr values for Holocene accumulations of salts show a bimodal distribution: high values between 225-1075 m.a.s.l. (0.70807 ± 0.00004) and low values below and above those altitude thresholds (0.70746 ± 0.00010). We sampled dated gypsic relict soils and Gypsisols to study post-5 Ma surface height evolution using this method, after correcting for changes in the altitudinal structure of the paleo-fog zone with time. Locations spanning ~250 km strike-parallel distance within the forearc and at elevations between 450-1650 m.a.s.l. display moderate amounts of altitudinal change during the Pliocene, Pleistocene and Quaternary. Site results include two in the northern zone (19.5ºS and 19.65ºS) that experienced maximum net surface uplifts of ~350 m and ~600 m since 2.5 ± 0.5 Ma and ~2.6 Ma, respectively. Locations at ~21.4°S display an estimated minimum net decline in altitude of ~250 m since 3.4 ± 1.1 Ma and ~200 m since 1.1 ± 0.4 Ma. These constraints will shed light on the geodynamic processes responsible for surface elevation change, by acting as boundary conditions to numerical models of the Andean forearc.

  20. 87Sr/86Sr in spinel peridotites from Borée, Massif Central, France: melt depletion and metasomatism in the sub-continental lithospheric mantle

    NASA Astrophysics Data System (ADS)

    Barnett, Caroline; Harvey, Jason

    2016-04-01

    Radiogenic isotopes and elemental concentrations in peridotite xenoliths may be used to model the timing and degree of partial melting in the upper mantle, but this primary melt depletion signature may be overwritten by subsequent episodes of melt or fluid infiltration. Spinel peridotites from the Maar de Borée, Massif Central, France have mainly poikilitic protogranular textures and clear petrographic evidence of a melt phase apparently unrelated to host basalt infiltration. Bulk rock major and compatible trace element concentrations are consistent with varying degrees of partial melting but incompatible trace element concentrations indicate cryptic metasomatism in some samples. Lithophile trace element mass balance cannot always be reconciled by the inclusion of the chemically characterized melt phase and suggest a contribution from a trace abundance grain boundary phase1. 87Sr/86Sr values for unleached bulk rocks and clinopyroxene mineral separates are higher than those for their leached equivalents, consistent with the removal of a radiogenic grain boundary phase. While unleached bulk rock 87Sr/86Sr is sometimes indistinguishable (within error) from its constituent unleached clinopyroxene, in two samples they show distinct patterns, as do the REE trends in these two xenoliths. BO01-01 bulk-rock is LREE-enriched (La/YbN = 3.6)2, and constituent clinopyroxene shows a similar relative enrichment trend. Bulk-rock 87Sr/86Sr is 0.70342±1 while that of clinopyroxene is lower at 0.70332±2. Clinopyroxene modal abundance is 11%. BO01-03 bulk-rock is only slightly LREE-enriched (La/YbN = 1.2) and both bulk-rock and clinopyroxene show a generally flatter profile. Bulk-rock 87Sr/86Sr is 0.70285±1 while that of clinopyroxene is in this case higher at 0.70296±2. Clinopyroxene modal abundance is also higher at 15%, consistent with a greater contribution by clinopyroxene to the bulk-rock Sr-isotope budget. The results appear to be inconsistent with a simple model of single

  1. Ge/Si, Ca/Sr and 87Sr/86Sr tracers of biogeochemical sources and cycling of Si and Ca at the Shale Hills CZO

    NASA Astrophysics Data System (ADS)

    Derry, L. A.; Meek, K.; Sparks, J. P.

    2014-12-01

    Plant uptake and cycling of nutrients is commonly the largest flux of nutrients in terrestrial ecosystems. Hydrologic and other losses are offset by inputs from atmospheric deposition and weathering. We measured elemental and isotopic compositions from soil solution, soil exchange complex, leaves and sapwater from two canopy species, soil and rock samples, and stream and ground waters at the Shale Hills CZO. Xylem fluid and leaf samples have similar Ge/Si < 1 μmo/mol, consistent with fractionation at the root-soil water interface. Ge/Si in soil waters is higher Ge/Si near the surface and increases over the growing season, indicating preferential uptake of Si. Ca/Sr in leaves of Quercus are significantly higher (450±150) than for Acer (200±100), and Ca/Sr is generally higher in leaves than in xylem, consistent with Ca uptake during transpiration. 87Sr/86Sr in both are similar for a given site, implying that the trees access similar pools of Sr and Ca, although there are site-to-site differences. Data on litterfall rates and transpiration rates yield similar estimates of plant cycling of Ca and Si. 87Sr/86Sr in soil solutions from ridgtop and swale sites are well explained by mixing Sr derived from shale and atmospheric deposition. Valley bottom soil solutions and stream and groundwater samples include Sr and Ca derived from dissolution of diagenetic carbonates, found in drill cuttings. A preliminary estimate of the Sr and Ca stream fluxes and isotopic mass balances imply propagation of a carbonate weathering front of ca. 200 m/Ma, faster than previously reported regolith weathering advance rates based on on cosmogenic nuclides and U series (Jin et al., 2010; Ma et al., 2010). These rates are not strictly comparable and differences are at least in part consistent with the greater depth of the carbonate weathering front (Brantley et al, 2013). The data for Ca, Sr, Si and Ge in soil, soil solutions and stream waters reflects the interaction of slower weathering

  2. Seawater and basalt-derived [sup 87]Sr/[sup 86]Sr in multiple dolomitization events, Seroe Domi Formation, Curacao, Netherlands Antilles

    SciTech Connect

    Fouke, B.W.; Meyers, W.J.; Hanson, G.N. . Dept. of Earth and Space Sciences); Beets, C.J. . Geomarine Centre)

    1992-01-01

    The distribution, petrography and geochemistry of Seroe Domi Formation Dolomites I, I[prime] and II are consistent with precipitation from seawater and/or seawater-dominated mixed fluids. Stratigraphic distributions and secular variations in the Sr-87/86-Sr of neogene seawater suggests that Dolomite I precipitated from Late Miocene seawater, Dolomite I[prime] precipitated from early Pliocene seawater, and Dolomite II precipitated from Plio-Pleistocene seawater. However, while Dolomite I and I[prime] are more radiogenic than their host Middle Miocene limestones, Dolomite II is equal to or less radiogenic than its host Pliocene limestone. Dolomite II is also enriched in Zn and Cu relative to Dolomites I and I[prime]. Biomoldic porosity, skeletal diagenesis and calcite cementation suggest that the host Seroe Domi limestones were extensively leached and recrystallized in meteoric fluids prior to dolomitization. Therefore, the only viable source of the nonradiogenic Sr in Dolomite II was through low-temperature groundwater interaction with altered basalts of the Curacao basement. Less radiogenic Sr was not incorporated in Dolomite I and I[prime] because the basalt had not yet been adequately weathered, or was not in hydrologic contact with Seroe Domi carbonates until the Pliocene or Pleistocene due to the thousands of meters of tectonic uplift and erosion of the Curacao basement. The anomalously high Sr/Ca and HCO[sub 3] abundances and non-radiogenic Sr-87/Sr-86 of modern groundwaters within the Curacao Lava Formation further substantiate this interpretation. Modeling with REACT implies that these meteoric groundwaters are supersaturated with respect to both dolomite and calcite, and that less than 20% of this Curacao groundwater in a mixture with Pleistocene seawater could have created the Sr-87/Sr-86 observed in Dolomite II.

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

    NASA Astrophysics Data System (ADS)

    Chen, Daizhao; Qing, Hairuo; Li, Renwei

    2005-06-01

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

  4. Evidence for early Pliocene and late Miocene transgressions in southern Patagonia (Argentina): 87Sr/86Sr ages of the pectinid “Chlamys” actinodes (Sowerby)

    NASA Astrophysics Data System (ADS)

    del Río, Claudia J.; Griffin, Miguel; McArthur, John M.; Martínez, Sergio; Thirlwall, Matthew F.

    2013-11-01

    Numerical ages based on 87Sr/86Sr dating of calcitic shells belonging to the pectinid “Chlamys” actinodes (Sowerby) document the only late Miocene (Tortonian) sea flooding event in the Austral Basin at Cabo Buentiempo (8.95 ± 0.82 Ma, 2 s.e.), and provide evidence of the first documented early Pliocene (Zanclean) transgression in Argentina recorded at Cañadón Darwin (5.15 ± 0.18 Ma, 2 s.e., Austral Basin) and at Terraces of Cerro Laciar (5.10 ± 0.21 Ma, 2 s.e.), southern San Jorge Basin). The sedimentary rocks deposited during the Tortonian are correlated with the youngest beds deposited by the “Entrerriense Sea” that covered northern Patagonia. The Zanclean marine episode is correlated with the long-term cycle represented in the Southern Hemisphere by the flooding events recorded in Cockburn and James Ross Islands (Antarctica) and in North-Central Chile.

  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

    SciTech Connect

    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 the 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.

  6. Chemical dynamics of the "St. Lawrence" riverine system: δD H 2O, δ 18O H 2O, δ 13C DIC, δ 34S sulfate, and dissolved 87Sr/ 86Sr

    NASA Astrophysics Data System (ADS)

    Yang, Chao; Telmer, Kevin; Veizer, Ján

    1996-03-01

    Chemical and stable isotope analyses of the St. Clair, Detroit, Niagara, and St. Lawrence rivers ("St. Lawrence" system) and their tributaries show that the chemical and isotopic compositions of the waters are strongly controlled by the geology of their drainage basins. Tributaries draining the Canadian Shield have very low TDS, HCO 3-, SO 42-, Ca 2+, Mg 2+, NO 3-, Sr 2+, higher Si and Fe total, and high 87Sr/ 86Sr ratios (0.710-0.713). The Grand and Thames rivers that drain Paleozoic limestones, dolostones, and evaporites are characterized by opposite attributes. The "St. Lawrence" and the tributaries draining the Canadian Appalachians fall between these two endmembers. The St. Clair, Detroit, and Niagara rivers do not show any pronounced seasonal variations in major component chemistry due to buffering by the Great Lakes. In contrast, pronounced seasonal variations characterize the lower St. Lawrence mainly because of significant tributary inputs into the overall water budget. The δD and δ18O in the "St. Lawrence" range from -60.9 to -44.5‰ and from -8.5 to -6.1‰ SMOW, respectively, much heavier than the comparative values measured for the tributaries (-92.8 to -58.3‰ and -13.1 to -8.5‰). This is a consequence of evaporative loss that, over the residence time of water of 10 2 years, equals about 7% of the water volume in the Great Lakes. The strontium and sulfur isotopic values for the "St. Lawrence" system are relatively uniform, with measured values from 0.70927 to 0.71112 for 87Sr/ 86Sr and from 4.3 to 5.6‰ for sulfate δ34S. Their seasonal variations are also minor. The strontium and sulfur fluxes of the St. Lawrence river are calculated to be 7.84 × 10 8 and 1.09 × 10 11 mol/a, respectively. The relative contributions of the Great Lakes, tributaries, and other sources to these fluxes are 73:16:11% for strontium and 64:13:23% for sulfur. Isotopic composition of dissolved inorganic carbon ( δ13C DIC) in the "St. Lawrence" system ranges from -4

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

    NASA Astrophysics Data System (ADS)

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

    2013-01-01

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

  8. 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

  9. 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

    SciTech Connect

    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 region 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.

  10. 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

    SciTech Connect

    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 region 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.

  11. Frequency Ratio of (199)Hg and (87)Sr Optical Lattice Clocks beyond the SI Limit.

    PubMed

    Yamanaka, Kazuhiro; Ohmae, Noriaki; Ushijima, Ichiro; Takamoto, Masao; Katori, Hidetoshi

    2015-06-12

    We report on a frequency ratio measurement of a (199)Hg-based optical lattice clock referencing a (87)Sr-based clock. Evaluations of lattice light shift, including atomic-motion-dependent shift, enable us to achieve a total systematic uncertainty of 7.2×10(-17) for the Hg clock. The frequency ratio is measured to be νHg/νSr=2.629 314 209 898 909 60(22) with a fractional uncertainty of 8.4×10(-17), which is smaller than the uncertainty of the realization of the International System of Units (SI) second, i.e., the SI limit.

  12. Frequency Ratio of (199)Hg and (87)Sr Optical Lattice Clocks beyond the SI Limit.

    PubMed

    Yamanaka, Kazuhiro; Ohmae, Noriaki; Ushijima, Ichiro; Takamoto, Masao; Katori, Hidetoshi

    2015-06-12

    We report on a frequency ratio measurement of a (199)Hg-based optical lattice clock referencing a (87)Sr-based clock. Evaluations of lattice light shift, including atomic-motion-dependent shift, enable us to achieve a total systematic uncertainty of 7.2×10(-17) for the Hg clock. The frequency ratio is measured to be νHg/νSr=2.629 314 209 898 909 60(22) with a fractional uncertainty of 8.4×10(-17), which is smaller than the uncertainty of the realization of the International System of Units (SI) second, i.e., the SI limit. PMID:26196788

  13. Frequency ratio measurement of 171Yb and 87Sr optical lattice clocks.

    PubMed

    Akamatsu, Daisuke; Yasuda, Masami; Inaba, Hajime; Hosaka, Kazumoto; Tanabe, Takehiko; Onae, Atsushi; Hong, Feng-Lei

    2014-04-01

    The frequency ratio of the (1)S(0)(F = 1/2)-(3)P(0)(F = 1/2) clock transition in (171)Yb and the (1)S(0)(F = 9/2)-(3)P(0)(F = 9/2) clock transition in (87)Sr is measured by an optical-optical direct frequency link between two optical lattice clocks. We determined the ratio (ν(Yb)/ν(Sr)) to be 1.207 507 039 343 341 2(17) fractional standard uncertainty of 1.4 × 10(-15) [corrected]. The measurement uncertainty of the frequency ratio is smaller than that obtained from absolute frequency measurements using the International Atomic Time (TAI) link. The measured ratio agrees well with that derived from the absolute frequency measurement results obtained at NIST and JILA, Boulder, CO using their Cs-fountain clock. Our measurement enables the first international comparison of the frequency ratios of optical clocks. The measured frequency ratio will be reported to the International Committee for Weights and Measures for a discussion related to the redefinition of the second.

  14. Frequency ratio measurement of 171Yb and 87Sr optical lattice clocks.

    PubMed

    Akamatsu, Daisuke; Yasuda, Masami; Inaba, Hajime; Hosaka, Kazumoto; Tanabe, Takehiko; Onae, Atsushi; Hong, Feng-Lei

    2014-04-01

    The frequency ratio of the (1)S(0)(F = 1/2)-(3)P(0)(F = 1/2) clock transition in (171)Yb and the (1)S(0)(F = 9/2)-(3)P(0)(F = 9/2) clock transition in (87)Sr is measured by an optical-optical direct frequency link between two optical lattice clocks. We determined the ratio (ν(Yb)/ν(Sr)) to be 1.207 507 039 343 341 2(17) fractional standard uncertainty of 1.4 × 10(-15) [corrected]. The measurement uncertainty of the frequency ratio is smaller than that obtained from absolute frequency measurements using the International Atomic Time (TAI) link. The measured ratio agrees well with that derived from the absolute frequency measurement results obtained at NIST and JILA, Boulder, CO using their Cs-fountain clock. Our measurement enables the first international comparison of the frequency ratios of optical clocks. The measured frequency ratio will be reported to the International Committee for Weights and Measures for a discussion related to the redefinition of the second. PMID:24718165

  15. Sr stable isotope variations in an evolved rhyolitic volcanic system investigated using an 84Sr-87Sr double spike

    NASA Astrophysics Data System (ADS)

    Charlier, B. L.; Wilson, C. J.; Parkinson, I.; Mueller, W.

    2013-12-01

    Strontium is a refractory lithophile element with four stable isotopes: 84Sr, 86Sr, 87Sr and 88Sr . However, 87Sr is also produced by the long-lived radioactive decay of 87Rb, and this parent-daughter isotope system has long been a key pillar of geochronology and geochemical tracing. Conventional Sr isotopic measurements made using TIMS or MC-ICP-MS are corrected for instrumental mass fractionation assuming a value for the 88Sr/86Sr ratio of 8.375209. This internal normalisation permits the measurement of 87Sr/86Sr ratios to a very high precision. However, normalisation to a fixed 88Sr/86Sr ratio using a mass-dependent fractionation law assumes that the stable isotope ratio is uniform in natural samples and erases the possible signature of any mass-dependent natural variation in the 88Sr/86Sr and 84Sr/86Sr ratios. In addition, normalization to a canonical value of 88Sr/86Sr can result in 87Sr/86Sr values that may be in error depending on the mass fractionation term used for internal normalisation. In this study, we present high-precision Sr stable (δ88Sr and δ84Sr) and radiogenic isotope data (87Sr/86Sr), determined using a double spike and TIMS, along with trace element data for a suite of samples from a single evolved volcanic system (Huckleberry Ridge Tuff [HRT], Yellowstone). The double spike technique permits the ';true' isotopic composition for all Sr isotope ratios to be determined (against the NBS987 standard) without recourse to conventional internal nomalisation. Strontium stable isotope values vary by up to ~0.5 ‰ in δ88Sr, and correlate well with Ba and Eu/Eu* variations in whole rocks and glass separates. Single sanidine crystals, on the other hand, record much a much larger range in δ88Sr and correlate well with 87Sr/86Sr. Our data suggest that crystallisation of sanidine (× plagioclase) and/or mixing of melts that have experienced such crystal fractionation can drive the bulk-rock or glass stable-Sr composition in tune with other indicators of

  16. Strontium Isotope Fractionation in the marine Realm: first application of a 87Sr/84Sr-Double Spike

    NASA Astrophysics Data System (ADS)

    Eisenhauer, A.; Krabbenhöft, A.; Böhm, F.; Liebetrau, V.; Fietzke, J.; Augustin, N.; Peucker-Ehrenbrink, B.; Vollstaedt, H.

    2009-04-01

    In order to precisely determine 88Sr/86Sr- and 87Sr/86Sr-isotope variations in natural samples using TIMS-technique we developed a mixed 87Sr/84Sr-double spike from two solutions enriched in 84Sr and 87Sr, respectively. After mixing the two solutions the Sr-spike ratios have precisely been determined by calibration to the NBS 987 standard. For the determination of natural 88Sr/86Sr- and 87Sr/86Sr-isotope variations in carbonates and silicates two TIMS measurements are required: an unspiked and a spiked run where the Sr-isotope ratios are arbitrarily normalized to a fixed Sr isotope ratio (e.g. mean of the first block). For denormalization and data reduction we adopted the algorithm for Ca isotope measurements (1) presented earlier by Heuser et al.(2003) modified for Sr-isotope measurements. It was found that best results can be achieved if the 84Srspike/84Srsample ratio is higher than about 12. The algorithm allows the simultaneous calculation of 87Sr/86Sr and 88Sr/86Sr ratios. Standard measurements showed a ^88•86Sr-value (^88•86Sr=((88Sr/86Sr)Sample/(88Sr/86Sr)SRM987)-1)*1000) of 0.39 for the IAPSO seawater standard corresponding to an external reproducibility of ±0.012 (n=19). The IAPSO ^88•86Sr-value corresponds to a 87Sr/86Sr-ratio of 0.709317(9). Both values are in accordance with earlier publications (2) and theoretical predictions based on the ^88•86Sr ratio of seawater and assuming mass-dependent isotope fractionation. This technique allows us to correct the 88Sr/86Sr- and 87Sr/86Sr-isotope-ratios for mass dependent fractionation during both column chemistry and TIMS measurement procedure. Furthermore a direct comparison of double spike TIMS, bracketing standard and laser-ablation MC-ICP-MS (3) results are in agreement and can be used to discuss limitation and perspectives of future Sr isotope measurements. References: 1 Heuser A., Eisenhauer A., Gussone N., Bock B., Hansen B.T. and Nägler Th.F. (2003) Measurement of Calcium Isotopes (^44Ca) Using a

  17. Modelling the Phanerozoic carbon cycle and climate - Constraints from the Sr-87/Sr-86 isotopic ratio of seawater

    NASA Technical Reports Server (NTRS)

    Francois, Louis M.; Walker, James C. G.

    1992-01-01

    A numerical model is developed for simulating the long-term changes of atmospheric CO2 and climate during the Phanerozoic. The model describes the coupled evolution of the biogeochemical cycles of C, S, Ca, Mg, P, and Sr, with the emphasis on the effect of coupling the cycles of carbon and strontium and on interpreting the observed seawater Sr-87/Sr-86 ratios. The abilities of continental weathering, volcanism, and surface lithology in generating that signal are tested and compared. The results obtained are used to reconstruct a history of atmospheric CO2 and climate during Phanerozoic time, consistent with the strontium isotopic data. It is shown that the predicted history is compatible with paleoclimatic indicators, such as the timing of glaciation and the estimates of Cretaceous paleotemperatures.

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

    NASA Astrophysics Data System (ADS)

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

    2008-12-01

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

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

    NASA Astrophysics Data System (ADS)

    Hartman, Gideon; Richards, Mike

    2014-02-01

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

  20. Chondrites: initial strontium-87/strontium-86 ratios and the early history of the solar system.

    PubMed

    Wetherill, G W; Mark, R; Lee-Hu, C

    1973-10-19

    A sodium-poor, calcium-rich inclusion in the carbonaceous chondrite Allende had a (87)Sr/(86)Sr ratio at the time of its formation of 0.69880, as low a value as that found in any other meteorite. The higher (87)Sr/(86)Sr ratios found in ordinary chondrites indicate that their formation or isotopic equilibration occurred tens of millions of years later.

  1. 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.

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

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

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

  3. 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). PMID:24971992

  4. 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).

  5. Weathering in and Calcium Losses From Semi-Arid Agricultural Landscapes: Insight From Strontium Isotope Ratios

    NASA Astrophysics Data System (ADS)

    Suzuki, K.; Keller, C.; Vervoort, J. D.

    2004-12-01

    The strontium isotope ratio (87Sr/86Sr) has been used in a number of recent studies of calcium cycling in forested ecosystems. In this research 87Sr/86Sr was used to investigate weathering and, specifically, seasonal variation of calcium loss in drainage from semi-arid, agricultural landscapes in the Palouse Region of Washington State, USA. The Palouse is dominated by rolling loess hills. The soils are silt-loam Mollisols and the predominant origin of the loess substrate is continental crust. Tile drains are widely used to improve drainage of lower-slope fields. 87Sr/86Sr of tile drainage, soil water, stream water and precipitation water were measured by multiple-collector Inductively Coupled Plasma Mass Spectrometry. 87Sr/86Sr of precipitation waters exhibited considerable variation (0.708 to 0.713). 87Sr/86Sr of the other water samples ranged from 0.707 to 0.708. These values are not close to continental crust values (0.716) but are more similar to basalts (0.702 to 0.707). 87Sr/86Sr of tile drainage appeared to be negatively correlated with discharge during the rainy season. Thus it appears that sources of dissolved calcium in drainage vary seasonally. Results of this work may help predict the soil-acidification effects of heavy loading of these systems with ammonia-N fertilizers.

  6. Fine resolution chronology based on initial Sr-87/Sr-86

    NASA Technical Reports Server (NTRS)

    Stewart, B. W.; Papanastassiou, D. A.; Capo, R. C.; Wasserburg, G. J.

    1993-01-01

    It has been recognized that small variations in initial Sr-87/Sr-86 (Sr(sub I)), can provide a fine scale relative chronology for the chemical fractionation of materials with low Rb/Sr from parent reservoirs with high Rb/Sr. Similarly, Sr(sub I), as determined for low Rb/Sr phases in meteorites, may permit a fine resolution chronology of the recrystallization or metamorphism of planetary materials. For the establishment of a primitive Sr-87/Sr-86 chronology, it is important to search for samples with extremely low Rb/Sr for which the measured Sr-87/Sr-86 is below BABI, in which case the primitive nature of the Sr can be directly established. Using the measured Rb/Sr to calculate an initial Sr-87/Sr-86 can introduce substantial uncertainty if the Rb-Sr are disturbed. We report Sr-87/Sr-86 in plagioclase from silicate pebbles from the Vaca Muerta mesosiderite on which we have reported Sm-147-Nd-143 and Ne-142 correlations. For the purpose of cross-calibration with our previous work we have performed extensive new measurements on Angra dos Reis and on anorthite from Moore County, which have very low Rb/Sr and primitive Sr-87/Sr-86.

  7. Chondrite chronology by initial Sr-87/Sr-86 in phosphates?

    NASA Technical Reports Server (NTRS)

    Podosek, Frank A.; Brannon, Joyce C.

    1991-01-01

    New data are presented on Rb-Sr isotope analyses of phosphates from nine ordinary chondrites, including accurate identification of initial Sr-87/Sr-86. The initial Sr-87/Sr-86 ratios found in this study were generally significantly higher than the more primitive initial Sr-87/Sr-86 ratios inferred for carbonaceous chondrite refractory inclusions, basaltic achondrites, or bulk ordinary chondrites. Such elevation of initial Sr-87/Sr-86 is generally considered to reflect isotopic redistribution during metamorphism. However, in this study, no evident correlation was found between the phosphate initial Sr-87/Sr-86 compositions and the metamorphic grade. Two possible alternative hypotheses for high initial Sr-87/Sr-86 ratios are considered.

  8. Stable Strontium Isotopes (δ88/86Sr) As a Tracer of Sr Sources and Biogeochemical Cycling in Two Catchments Draining Fiordland, New Zealand

    NASA Astrophysics Data System (ADS)

    Andrews, G.; Jacobson, A. D.; Lehn, G. O.

    2014-12-01

    To understand how Sr isotopes behave during chemical weathering and biogeochemical cycling, we analyzed the stable Sr isotope composition (δ88/86Sr) of rivers, rocks, sediments, plants, and soils from the Cleddau and Hollyford catchments in Fiordland, New Zealand. We leached rocks, sediments, and soils to isolate relatively soluble Sr sources. δ88/86Sr values were measured using an 87Sr-84Sr double-spike MC-TIMS method, which was optimized according to the Monte Carlo error model described in Lehn et al. (2013). The long-term, external reproducibility of the method is ±0.020‰ (2σSD) based on repeated measurements of NBS-987 [δ88/86Sr = 0.000 ± 0.004‰ (2σSEM), n=77] and IAPSO seawater [δ88/86Sr = 0.396 ± 0.005‰ (2σSEM), n=54]. Although the study site receives abundant rainfall (6700mm/yr), atmospheric inputs of Sr are negligible. We find that δ88/86Sr values can distinguish between silicate- versus carbonate- derived riverine Sr sources when traditional tracers, such as radiogenic Sr isotope (87Sr/86Sr) and molar Ca/Sr ratios, are equivocal. Moreover, rivers draining gabbro bedrock in the Cleddau and Upper Hollyford catchments have higher δ88/86Sr values (0.368‰) as compared to bulk silicate rock (0.162 - 0.284‰) and sediment (0.286‰). In the Lower Hollyford catchment, tributary rivers draining volcanic and sedimentary rocks also have higher δ88/86Sr values (0.328‰) as compared to bulk silicate rock (0.177‰) and sediment (0.260‰). We examine several hypotheses to explain the elevated riverine δ88/86Sr values, including end-member mixing, fractionation during chemical weathering, and plant uptake. We attribute the riverine δ88/86Sr values to mixing with the soil pore water pool, which is isotopically heavy due to preferential uptake of 86Sr by plants.

  9. Upper Cenozoic basalts with high Sr-87/Sr-86 and Sr/Rb ratios, southern Great Basin, western United States.

    NASA Technical Reports Server (NTRS)

    Hedge, C. E.; Noble, D. C.

    1971-01-01

    The initial strontium isotopic composition of 15 mafic volcanic rocks from the southern Great Basin has been determined. Results indicate that the basalts must have been derived from unusual mantle material in which an originally high Rb/Sr ratio was markedly lowered during an earlier phase of magmatic activity.

  10. Tracking mammoths and mastodons: Reconstruction of migratory behavior using strontium isotope ratios

    NASA Astrophysics Data System (ADS)

    Hoppe, Kathryn A.; Koch, Paul L.; Carlson, Richard W.; Webb, S. David

    1999-05-01

    Variations in the strontium isotope ratio (87Sr/86Sr) of tooth enamel are used to examine the migration patterns of late Pleistocene mammoths and mastodons from Florida. An animal's 87Sr/86Sr ratio tracks the ratios of its environment, which vary with differences in bedrock and soil. Consequently, the environmentally controlled differences in 87Sr/86Sr ratio recorded in mineralized tissue, such as tooth enamel, may be used to reconstruct the movement patterns of an individual. We map variations in local 87Sr/86Sr ratios across modern Florida and Georgia through analysis of rodent teeth, plants, and surface water, then use this map to interpret the movement patterns of extinct mammals. Mastodons from northern and central Florida have higher 87Sr/86Sr ratios than both modern environmental samples from Florida and fossils from nonmigratory species, suggesting that mastodons migrated north into Georgia. Mammoths display ratios similar to those of environmental samples and resident species, suggesting that they did not migrate outside Florida.

  11. Rapid exchange effects on isotope ratios in groundwater systems: 2. Flow investigation using Sr isotope ratios

    NASA Astrophysics Data System (ADS)

    Johnson, Thomas M.; Depaolo, Donald J.

    1997-01-01

    Sr isotope ratios were measured in groundwater, whole rock digestions, and cation exchange extracts from a clay-rich groundwater system at Ernest O. Lawrence Berkeley National Laboratory and were used to constrain flow velocities and search for preferential flow paths. In the Orinda formation siltstone, 87Sr/86Sr increases strongly over tens of meters along presumed flow paths, indicating slow groundwater flow. Dissolved Sr is close to isotopic equilibrium with the exchangeable Sr in the clays, and the observed 87Sr/86Sr increase is interpreted as a cation exchange front moving slowly through the unit combined with dissolution of minerals with relatively high 87Sr/86Sr ratios. The data are inverted using a one-dimensional transport-dissolution-exchange model; the results indicate long-term average flow velocities of less than 0.2 m/yr which are consistent with 14C measurements. The data suggest a lack of strong preferential flow paths through this unit.

  12. 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.

  13. Groundwater ''fast paths'' in the Snake River plain aquifer: Radiogenic isotope ratios as natural groundwater tracers

    SciTech Connect

    Johnson, Thomas M.; Roback, Robert C.; McLing, Travis L.; Bullen, Thomas D.; DePaolo, Donald J.; Doughty, Christine; Hunt, Randall J.; Smith, Robert W.; Cecil, L. DeWayne; Murrell, Michael T.

    2000-09-01

    Preferential flow paths are expected in many groundwater systems and must be located because they can greatly affect contaminant transport. The fundamental characteristics of radiogenic isotope ratios in chemically evolving waters make them highly effective as preferential flow path indicators. These ratios tend to be more easily interpreted than solute-concentration data because their response to water-rock interaction is less complex. We demonstrate this approach with groundwater {sup 87}Sr/{sup 86}Sr ratios in the Snake River Plain aquifer within and near the Idaho National Engineering and Environmental Laboratory. These data reveal slow-flow zones as lower {sup 87}Sr/{sup 86}Sr areas created by prolonged interaction with the host basalts and a relatively fast flowing zone as a high {sup 87}Sr/{sup 86}Sr area.

  14. Neutron Capture from 87Sr

    NASA Astrophysics Data System (ADS)

    Rusev, G.; Raut, R.; Tonchev, A. P.; Tornow, W.; Baramsai, B.; Kelley, J. H.; Mitchell, G.; Bredeweg, T.; Couture, A.; Jandel, M.; O'Donnell, J.; Rundberg, R.; Ullmann, J. L.; Chyzh, A.; Kwan, E.

    2011-10-01

    The neutron-capture resonances of the reaction 87Sr(n , γ)88Sr are significant to nuclear astrophysics to estimate the neutron density during the s process, whose path is split by the branching nucleus 85Kr, and for a possible use of the 87Rb-87Sr chronometric pair to measure the age of our Galaxy. In addition, the γ rays of the product nucleus 88Sr are of importance to nuclear structure and the study of the pygmy resonance observed earlier in (γ ,γ') measurements. We report results from a neutron-capture experiment on 87Sr carried out with the 4 π BaF2 array, DANCE, at LANL. Spin values of neutron resonances have been deduced using the multiplicity and angular distributions of the cascade γ rays following the neutron capture. Work supported by the US Department of Energy under grants DE-FG02-97ER41033, DE-FG02-97ER41042, DE-FG02-97ER41041, and DE-FG52-06NA26155.

  15. 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

  16. Influences on 87Sr/86Sr in the British biosphere beyond bedrock.

    NASA Astrophysics Data System (ADS)

    Evans, Jane; Warham, Joseph; Ander, Louise; Montgomery, Janet

    2014-05-01

    Strontium enters the biosphere thought the uptake of the element by plants through their roots. Where the soil is derived by the erosion of underlying bedrock there is a relationship between the isotope compositions of the biosphere and the bedrock. This makes it possible to estimate biosphere Sr in places where the relationship exists and the isotope properties of the underlying rock are understood. Direct mapping, however, of the biosphere is preferable and increasingly undertaken and this is particularly important when non bedrock influences exist. For example, a layer of peat that detaches the isotope domain of the biosphere from the underlying rocks. This poster presents studies on the effect of altitude, sea and rainwater influences, superficial deposits such as peat, glacial till and dust, in order to refine the understanding of factors influencing biosphere Sr values and show how we are trying to develop the online British biosphere dataset (http://www.bgs.ac.uk/nigl/SBA_Maps.htm).

  17. The Phanerozoic δ88/86Sr record of seawater: New constraints on past changes in oceanic carbonate fluxes

    NASA Astrophysics Data System (ADS)

    Vollstaedt, Hauke; Eisenhauer, Anton; Wallmann, Klaus; Böhm, Florian; Fietzke, Jan; Liebetrau, Volker; Krabbenhöft, André; Farkaš, Juraj; Tomašových, Adam; Raddatz, Jacek; Veizer, Ján

    2014-03-01

    The isotopic composition of Phanerozoic marine sediments provides important information about changes in seawater chemistry. In particular, the radiogenic strontium isotope (87Sr/86Sr) system is a powerful tool for constraining plate tectonic processes and their influence on atmospheric CO2 concentrations. However, the 87Sr/86Sr isotope ratio of seawater is not sensitive to temporal changes in the marine strontium (Sr) output flux, which is primarily controlled by the burial of calcium carbonate (CaCO3) at the ocean floor. The Sr budget of the Phanerozoic ocean, including the associated changes in the amount of CaCO3 burial, is therefore only poorly constrained. Here, we present the first stable isotope record of Sr for Phanerozoic skeletal carbonates, and by inference for Phanerozoic seawater (δ88/86Srsw), which we find to be sensitive to imbalances in the Sr input and output fluxes. This δ88/86Srsw record varies from ˜0.25‰ to ˜0.60‰ (vs. SRM987) with a mean of ˜0.37‰. The fractionation factor between modern seawater and skeletal calcite Δ88/86Srcc-sw, based on the analysis of 13 modern brachiopods (mean δ88/86Sr of 0.176 ± 0.016‰, 2 standard deviations (s.d.)), is -0.21‰ and was found to be independent of species, water temperature, and habitat location. Overall, the Phanerozoic δ88/86Srsw record is positively correlated with the Ca isotope record (δ44/40Casw), but not with the radiogenic Sr isotope record ((87Sr/86Sr)sw). A new numerical modeling approach, which considers both δ88/86Srsw and (87Sr/86Sr)sw, yields improved estimates for Phanerozoic fluxes and concentrations for seawater Sr. The oceanic net carbonate flux of Sr (F(Sr)carb) varied between an output of -4.7 × 1010 mol/Myr and an input of +2.3 × 1010 mol/Myr with a mean of -1.6 × 1010 mol/Myr. On time scales in excess of 100 Myrs the F(Sr)carb is proposed to have been controlled by the relative importance of calcium carbonate precipitates during the “aragonite” and

  18. Fractionation of stable isotopes of strontium in continental carbonate environments as a potential contributor to the δ88/86Sr in the oceans

    NASA Astrophysics Data System (ADS)

    Shalev, Netta; Halicz, Ludwik; Stein, Mordechai; Gavrieli, Ittai; Sandler, Amir; Segal, Irena; Lazar, Boaz

    2014-05-01

    Several fluxes dictate the concentration and isotope composition of strontium in the oceans including: continental crust weathering, the hydrothermal flux and the precipitation of marine carbonates. These fluxes were traditionally evaluated by the radiogenic ratio of 87Sr/86Sr and recently by the stable isotope ratio of 88Sr/86Sr. In this study the Sr fractionation in carbonate continental environments were investigated in order to evaluate the continental weathering 88Sr/86Sr component. The δ88/86Sr values of mountain soils along a precipitation gradient and their parent desert dust were analyzed, as well as the δ88/86Sr values of continental waters that precipitated carbonate minerals. Isotopic measurements were conducted by MC-ICP-MS using double-spike method to correct for the instrumental mass bias. The results show that the desert dust and all mountain soils have a similar δ88/86Sr values. These results suggest that there is no significant Sr isotope fractionation during weathering (including leaching and dissolution). In contrast, we found significant Sr isotope fractionation during precipitation of continental solid carbonates. Speleothems and tufa were isotopically depleted with respect to the dripping and stream waters from which they precipitated. The Δ88/86Srcarb-water, the average isotope fractionation factor between the solid carbonate and the conjugate water was found to be -0.20±0.08o (2SD, n=5). This fractionation factor is similar within 2SD to the previously published Δ88/86Srcarb-water for precipitation of marine carbonates (Δ88/86Srcarb-sw=-0.24). The continental carbonate precipitation is substantially smaller than the marine carbonate deposition and hence has a little impact on the Sr isotopic composition of the continental runoff into the oceans. Our results indicate that δ88/86Sr value of the continental flux to the ocean is predominantly dictated by the relative contribution of Sr derived by weathering of two end members: silicates

  19. Neutron capture cross sections for /sup 86,87/Sr at Stellar temperatures

    SciTech Connect

    Bauer, R.W.; Mathews, G.J.; Becker, J.A.; Howe, R.E.

    1986-02-01

    Cross sections have been measured from 100 eV to 1 MeV by the neutron-time-of-flight technique. The capture events were recorded by detecting the prompt gamma-ray cascade with two C/sub 6/D/sub 6/ scintillators, and were normalized to standard gold cross sections. The background was determined experimentally by utilizing the ''black resonance'' technique. A /sup 6/Li-glass scintillator was used to monitor the neutron flux. A Maxwellian-averaged capture cross section at kT = 30 keV of 74 +- 3 mb for /sup 86/Sr, and 102 +- 4 mb for /sup 87/Sr. (LEW)

  20. 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.

  1. ^87Sr Clock Comparisons at JILA

    NASA Astrophysics Data System (ADS)

    Williams, Jason; Nicholson, Travis; Bloom, Benjamin; Campbell, Sara; Martin, Michael; Swallows, Matthew; Bishof, Michael; Ye, Jun

    2012-06-01

    Great advances are being realized with optical lattice clocks, where spectroscopy at optical frequencies and large ensembles of neutral atoms combine to offer extremely high frequency precision and stability. Recent results from the Strontium 87 optical atomic clock at JILA have demonstrated that strong interactions among fermions confined in a two-dimensional (2D) optical lattice suppress the collisional frequency shift and its uncertainty to the level of 10-17 [1]. We report on the progress of a second optical lattice clock at JILA, in which fermionic ^87Sr atoms are confined in a lattice potential derived from optical buildup cavities to provide strong confinement over a very large volume in one, two, and three dimensional lattices. Intercomparisons of the two clocks at JILA will be used to explore in greater detail the physics governing the transition shifts and uncertainties in our two ^87Sr optical lattice systems and will provide a significant improvement of our systematic errors.[4pt] [1] M D. Swallows et al. Science, 331, 1043 (2011)

  2. 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. PMID:27396661

  3. New limits on coupling of fundamental constants to gravity using 87Sr optical lattice clocks.

    PubMed

    Blatt, S; Ludlow, A D; Campbell, G K; Thomsen, J W; Zelevinsky, T; Boyd, M M; Ye, J; Baillard, X; Fouché, M; Le Targat, R; Brusch, A; Lemonde, P; Takamoto, M; Hong, F-L; Katori, H; Flambaum, V V

    2008-04-11

    The 1S0-3P0 clock transition frequency nuSr in neutral 87Sr has been measured relative to the Cs standard by three independent laboratories in Boulder, Paris, and Tokyo over the last three years. The agreement on the 1 x 10(-15) level makes nuSr the best agreed-upon optical atomic frequency. We combine periodic variations in the 87Sr clock frequency with 199Hg+ and H-maser data to test local position invariance by obtaining the strongest limits to date on gravitational-coupling coefficients for the fine-structure constant alpha, electron-proton mass ratio mu, and light quark mass. Furthermore, after 199Hg+, 171Yb+, and H, we add 87Sr as the fourth optical atomic clock species to enhance constraints on yearly drifts of alpha and mu.

  4. New Limits on Coupling of Fundamental Constants to Gravity Using {sup 87}Sr Optical Lattice Clocks

    SciTech Connect

    Blatt, S.; Ludlow, A. D.; Campbell, G. K.; Thomsen, J. W.; Zelevinsky, T.; Boyd, M. M.; Ye, J.; Baillard, X.; Fouche, M.; Le Targat, R.; Brusch, A.; Lemonde, P.; Takamoto, M.; Hong, F.-L.; Katori, H.; Flambaum, V. V.

    2008-04-11

    The {sup 1}S{sub 0}-{sup 3}P{sub 0} clock transition frequency {nu}{sub Sr} in neutral {sup 87}Sr has been measured relative to the Cs standard by three independent laboratories in Boulder, Paris, and Tokyo over the last three years. The agreement on the 1x10{sup -15} level makes {nu}{sub Sr} the best agreed-upon optical atomic frequency. We combine periodic variations in the {sup 87}Sr clock frequency with {sup 199}Hg{sup +} and H-maser data to test local position invariance by obtaining the strongest limits to date on gravitational-coupling coefficients for the fine-structure constant {alpha}, electron-proton mass ratio {mu}, and light quark mass. Furthermore, after {sup 199}Hg{sup +}, {sup 171}Yb{sup +}, and H, we add {sup 87}Sr as the fourth optical atomic clock species to enhance constraints on yearly drifts of {alpha} and {mu}.

  5. 88Sr/86Sr fractionation in inorganic aragonite and in corals

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2001-04-01

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

  7. 40K-40Ca and 87Rb-86Sr Dating by SIMS: The Double-Plus Advantage

    NASA Astrophysics Data System (ADS)

    Harrison, T. M.; McKeegan, K. D.; Schmitt, A. K.

    2009-12-01

    retentivity of 40Ca* relative to 40Ar* in white micas. This approach offers the potential to develop a branched-decay thermochronometer (K-Ca-Ar) permitting simultaneous solution of temperature-time history from μm-scale isotopic variations. A further advantage is that even low resolution SIMS instruments (e.g., ims7f) can utilize the double-plus method. Initial investigations using the same double-plus approach for Rb-Sr dating show promise. While resolving 87Rb+ from 87Sr+ requires an MRP of ~290k, unattainable using any current SIMS instrument, 87Rb++ is so strongly suppressed that determination of 87Sr++ is possible with minor peak stripping. 87Rb/86Sr can be determined either from 85Rb+/88Sr+ at MRP≈ 8k or by the use of energy filtering. In addition to micas, these approaches may be applicable to any mineral systems enriched in alkali metals relative to alkaline earths, such as alkali feldspars, feldspathoids, and alkaline halides.

  8. Accurate Optical Lattice Clock with {sup 87}Sr Atoms

    SciTech Connect

    Le Targat, Rodolphe; Baillard, Xavier; Fouche, Mathilde; Brusch, Anders; Tcherbakoff, Olivier; Rovera, Giovanni D.; Lemonde, Pierre

    2006-09-29

    We report a frequency measurement of the {sup 1}S{sub 0}-{sup 3}P{sub 0} transition of {sup 87}Sr atoms in an optical lattice clock. The frequency is determined to be 429 228 004 229 879(5) Hz with a fractional uncertainty that is comparable to state-of-the-art optical clocks with neutral atoms in free fall. The two previous measurements of this transition were found to disagree by about 2x10{sup -13}, i.e., almost 4 times the combined error bar and 4 to 5 orders of magnitude larger than the claimed ultimate accuracy of this new type of clocks. Our measurement is in agreement with one of these two values and essentially resolves this discrepancy.

  9. Evaluation of strontium isotope abundance ratios in combination with multi-elemental analysis as a possible tool to study the geographical origin of ciders.

    PubMed

    García-Ruiz, Silvia; Moldovan, Mariella; Fortunato, Giuseppino; Wunderli, Samuel; García Alonso, J Ignacio

    2007-05-01

    In order to evaluate alternative analytical methodologies to study the geographical origin of ciders, both multi-elemental analysis and Sr isotope abundance ratios in combination with multivariate statistical analysis were estimated in 67 samples from England, Switzerland, France and two Spanish regions (Asturias and the Basque Country). A methodology for the precise and accurate determination of the (87)Sr/(86)Sr isotope abundance ratio in ciders by multicollector inductively coupled plasma mass spectrometry (MC-ICP-MS) was developed. Major elements (Na, K, Ca and Mg) were measured by ICP-AES and minor and trace elements (Li, Be, B, Al, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Se, Rb, Sr, Y, Mo, Cd, Sn, Sb, Cs, Ba, La, Ce, W, Tl, Pb, Bi, Th and U) were measured by ICP-MS using a collision cell instrument operated in multitune mode. An analysis of variance (ANOVA test) indicated that group means for B, Cr, Fe, Ni, Cu, Se, Cd, Cs, Ce, W, Pb, Bi and U did not show any significant differences at the 95% confidence level, so these elements were rejected for further statistical analysis. Another group of elements (Li, Be, Sc, Co, Ga, Y, Sn, Sb, La, Tl, Th) was removed from the data set because concentrations were close to the limits of detection for many samples. Therefore, the remaining elements (Na, Mg, Al, K, Ca, Ti, V, Mn, Zn, As, Rb, Sr, Mo, Ba) together with (87)Sr/(86)Sr isotope abundance ratio were considered for principal component analysis (PCA) and linear discriminant analysis (LDA). Finally, LDA was able to classify correctly 100% of cider samples coming from different Spanish regions, France, England and Switzerland when considering Na, Mg, Al, K, Ca, Ti, V, Mn, Zn, As, Rb, Sr, Mo, Ba and (87)Sr/(86)Sr isotope abundance ratio as original variables. PMID:17416223

  10. 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.

  11. Water-Rock Interactions in the Peridotite Aquifer of the Oman-UAE Ophiolite: Strontium Isotopic Ratio and Geochemical Evolution of Groundwater

    NASA Astrophysics Data System (ADS)

    Bompard, Nicolas; Matter, Juerg; Teagle, Damon

    2016-04-01

    The peridotite aquifer in Wadi Tayin, Sultanate of Oman, is a perfect example of natural carbonation of ultramafic rocks. In situ mineral carbonation is considered the most safest and permanent option of CO2 Capture and Sequestration (CCS). However, the process itself is yet to be characterised and a better understanding of the mechanisms involved in natural mineral carbonation is needed before geo-engineering it. We used the 87Sr/86Sr system to follow the water-rock interactions along the groundwater flowpath in the peridotite aquifer and to determine the sources of divalent cations (Mg2+, Ca2+) required for mineral carbonation. The Sr-isotope data of groundwater show that the aquifer rocks are the main source for divalent cations (Mg2+, Ca2+ and Sr2+) and secondary carbonates are their main sink. The groundwater 87Sr/86Sr ratio evolves with its pH: from 87Sr/86Sr = 0.7087 (n=3) to 0.7082 (n=8) between pH 7 and 8, and from 0.7086 (n=6) at pH 9 to 0.07075 (n=9) at pH 11. This evolution seems to support a two-step model for the water-rock interactions in the peridotite aquifer. From pH 7 to 8, secondary Ca-carbonate precipitation buffers the pH rise resulting from peridotite serpentinisation. From pH 9 to 11, peridotite serpentinisation drives the pH to alkaline condition. The change from a Mg-rich to a Ca-rich groundwater at pH 9 seems to confirm the two-step model.

  12. Determining the geographical origin of Chinese cabbages using multielement composition and strontium isotope ratio analyses.

    PubMed

    Bong, Yeon-Sik; Shin, Woo-Jin; Gautam, Mukesh Kumar; Jeong, Youn-Joong; Lee, A-Reum; Jang, Chang-Soon; Lim, Yong-Pyo; Chung, Gong-Soo; Lee, Kwang-Sik

    2012-12-15

    Recently, the Korean market has seen many cases of Chinese cabbage (Brassica rapa ssp. pekinensis) that have been imported from China, yet are sold as a Korean product to illegally benefit from the price difference between the two products. This study aims to establish a method of distinguishing the geographical origin of Chinese cabbage. One hundred Chinese cabbage heads from Korea and 60 cabbage heads from China were subjected to multielement composition and strontium isotope ratio ((87)Sr/(86)Sr) analyses. The (87)Sr/(86)Sr ratio differed, based on the geological characteristics of their district of production. In addition, the content of many elements differed between cabbages from Korea and China. In particular, the difference in the content of Sr and Ti alone and the combination of Sr, Ca, and Mg allowed us to distinguish relatively well between Korea and China as the country of origin. The present study demonstrates that the chemical and Sr isotopic analyses exactly reflect the geology of the production areas of Chinese cabbage.

  13. Determining the geographical origin of Chinese cabbages using multielement composition and strontium isotope ratio analyses

    NASA Astrophysics Data System (ADS)

    BONG, Y.; Shin, W.; Gautam, M. K.; Jeong, Y.; Lee, A.; Jang, C.; Lim, Y.; Chung, G.; Lee, K.

    2012-12-01

    Recently, the Korean market has seen many cases of Chinese cabbage (Brassica rapa ssp. pekinensis) that have been imported from China, yet are sold as a Korean product to illegally benefit from the price difference between the two products. This study aims to establish a method of distinguishing the geographical origin of Chinese cabbage. One hundred Chinese cabbage heads from Korea and 60 cabbage heads from China were subjected to multielement composition and strontium isotope ratio (87Sr/86Sr) analyses. The 87Sr/86Sr ratio differed, based on the geological characteristics of their district of production. In addition, the content of many elements differed between cabbages from Korea and China. In particular, the difference in the content of Sr and Ti alone and the combination of Sr, Ca, and Mg allowed us to distinguish relatively well between Korea and China as the country of origin. The present study demonstrates that the chemical and Sr isotopic analyses exactly reflect the geology of the production areas of Chinese cabbage. Also, multivariate statistical analyses of multiple elements were found to be very effective in distinguishing the geographical origin of Chinese cabbages.

  14. 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 Astrophysics Data System (ADS)

    Podosek, F. A.; Zinner, E. K.; MacPherson, G. J.; Lundberg, L. L.; Brannon, J. C.; Fahey, A. J.

    1991-04-01

    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.

  15. 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 t

  16. 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 t

  17. Tracing freshwater plume migration in the estuary after a typhoon event using Sr isotopic ratios

    NASA Astrophysics Data System (ADS)

    Huang, Kuo-Fang; You, Chen-Feng

    2007-01-01

    Tracing the flow of estuarine water into the coastal ocean is complicated due to intense regional mixing and hydro-morphological restrictions. Here we apply high precision 87Sr/86Sr measurements (2σ = ±3 ppm) in estuarine waters, together with dissolved Ba and Mn, to trace freshened plumes after Typhoon Toraji. Small, but distinguishable Sr isotopic variations are detected in the Kao-ping Estuary, where Δ87Sr varied up to 50 ppm. On the basis of these geochemical constraints, two distinct sources with high Δ87Sr are identified, which subsequently mixed with the South China Sea Surface Water. The most radiogenic Sr source can be attributed to enhanced water-sediment interactions generated by the typhoon. An additional source of high 87Sr/86Sr is attributable to redox-transformation of suspended particles due to variations in river discharges.

  18. Boron and strontium isotope ratios and major/trace elements concentrations in tea leaves at four major tea growing gardens in Taiwan.

    PubMed

    Chang, Cheng-Ta; You, Chen-Feng; Aggarwal, Suresh Kumar; Chung, Chuan-Hsiung; Chao, Hung-Chun; Liu, Hou-Chun

    2016-06-01

    Isotopic compositions of B and Sr in rocks and sediments can be used as tracers for plant provincial sources. This study aims to test whether tea leaf origin can be discriminated using (10)B/(11)B and Sr isotopic composition data, along with concentrations of major/trace elements, in tea specimens collected from major plantation gardens in Taiwan. The tea leaves were digested by microwave and analyzed by multi-collector inductively coupled plasma mass spectrometry (MC-ICPMS). The data showed significant variations in (87)Sr/(86)Sr ratios (from 0.70482 to 0.71462), which reflect changes in soil, groundwater or irrigation conditions. The most radiogenic tea leaves were found at the Taitung garden and the least radiogenic ones were from the Hualien garden. The δ (11)B was found to change appreciably (δ (11)B = 0.38-23.73 ‰) which could be due to fertilizers. The maximum δ (11)B was also observed in tea samples from the Hualien garden. Principal component analysis combining (87)Sr/(86)Sr, δ (11)B and major/trace elements results successfully discriminated different sources of major tea gardens in Taiwan, except the Hualien gardens, and this may be due to rather complicated local geological settings. PMID:26254888

  19. Pulsed 86Sr-labeling and NanoSIMS imaging to study coral biomineralization at ultra-structural length scales

    NASA Astrophysics Data System (ADS)

    Brahmi, C.; Domart-Coulon, I.; Rougée, L.; Pyle, D. G.; Stolarski, J.; Mahoney, J. J.; Richmond, R. H.; Ostrander, G. K.; Meibom, A.

    2012-09-01

    A method to label marine biocarbonates is developed based on a concentration enrichment of a minor stable isotope of a trace element that is a natural component of seawater, resulting in the formation of biocarbonate with corresponding isotopic enrichments. This biocarbonate is subsequently imaged with a NanoSIMS ion microprobe to visualize the locations of the isotopic marker on sub-micrometric length scales, permitting resolution of all ultra-structural details. In this study, a scleractinian coral, Pocillopora damicornis, was labeled 3 times with 86Sr-enhanced seawater for a period of 48 h with 5 days under normal seawater conditions separating each labeling event. Two non-specific cellular stress biomarkers, glutathione-S-transferase activity and porphyrin concentration plus carbonic anhydrase, an enzymatic marker involved in the physiology of carbonate biomineralization, as well as unchanged levels of zooxanthellae photosynthesis efficiency indicate that coral physiological processes are not affected by the 86Sr-enhancement. NanoSIMS images of the 86Sr/44Ca ratio in skeleton formed during the experiment allow for a determination of the average extension rate of the two major ultra-structural components of the coral skeleton: Rapid Accretion Deposits are found to form on average about 4.5 times faster than Thickening Deposits. The method opens up new horizons in the study of biocarbonate formation because it holds the potential to observe growth of calcareous structures such as skeletons, shells, tests, spines formed by a wide range of organisms under essentially unperturbed physiological conditions.

  20. Internal Rb-Sr Age and Initial Sr-87/Sr-86 of a Silicate Inclusion from the Campo Del Cielo Iron Meteorite

    NASA Technical Reports Server (NTRS)

    Liu, Y.; Nyquist, L.; Wiesmann, H.; Shih, C.; Schwandt, C.; Takeda, H.

    2003-01-01

    The largest group of iron meteorites, IAB, is distinguished by the presence of diverse silicate inclusions. In principle, Rb-Sr and Sm-Nd radiometric dating of these silicate inclusions by internal isochron techniques can determine both the times of melting and parent/daughter ratios in the precursor materials via initial Sr-87/Sr-86 and Nd-143/Nd-144 ratios. The Sr-87/Sr-86 and Nd-143/Nd-144 ratios could distinguish chondritic precursors from already differentiated silicates. We reported Rb-Sr and Sm-Nd internal ischron ages of 4.52+/-0.03 Ga and 4.50+/-0.04 Ga, respectively, for plagioclase-diopside-rich material in the Caddo County IAB iron meteorite. These results are essentially identical to literature values of its Ar-Ar age of 4.520+/-0.005 Ga and its Sm-Nd age of 4.53+/-0.02 Ga. The purpose of this study is to evaluate the formation and evolution of silicate inclusions in IAB iron meteorites by determination of their initial Sr-87/Sr-86 ratios combined with higher-resolution chronology and mineralogical and geochemical studies.

  1. Gamma-ray spectra from neutron capture on /sup 87/Sr

    SciTech Connect

    Sullivan, R.E.; Becker, J.A.; Stelts, M.L.

    1981-07-01

    The gamma-ray spectrum following neutron capture on /sup 87/Sr was measured at 3 neutron energies: E/sub n/ = thermal, 2 keV, and 24 keV. Gamma rays were detected in a three-crystal Ge(Li)-NaI-NaI pair spectrometer. Gamma-ray intensities deduced from these spectra by spectral unfolding are presented.

  2. Variation in strontium isotope ratios of archaeological fauna in the Midwestern United States: a preliminary study

    USGS Publications Warehouse

    Hedman, Kristin M.; Curry, B. Brandon; Johnson, Thomas M.; Fullagar, Paul D.; Emerson, Thomas E.

    2009-01-01

    Strontium isotope values (87Sr/86Sr) in bone and tooth enamel have been used increasingly to identify non-local individuals within prehistoric human populations worldwide. Archaeological research in the Midwestern United States has increasingly highlighted the role of population movement in affecting interregional cultural change. However, the comparatively low level of geologic variation in the Midwestern United States might suggest a corresponding low level of strontium variation, and calls into question the sensitivity of strontium isotopes to identify non-local individuals in this region. Using strontium isotopes of archaeological fauna, we explore the degree of variability in strontium ratios across this region. Our results demonstrate measurable variation in strontium ratios and indicate the potential of strontium analysis for addressing questions of origin and population movement in the Midwestern United States.

  3. Superradiance on the mHz linewidth clock transition in 87Sr

    NASA Astrophysics Data System (ADS)

    Norcia, Matthew; Winchester, Matthew; Cline, Julia; Thompson, James

    2016-05-01

    In this talk, I will discuss our recent experimental explorations of superradiant emission from the mHz linewidth clock transition in an ensemble of cold 87 Sr atoms confined within a high-finesse optical cavity. Recent proposals suggest that superradiant lasers based on such dipole-forbidden transitions in alkaline earth atoms could achieve linewidths below the current state of the art, with reduced sensitivity to environmental perturbations.

  4. Determination of the geographic origin of rice by chemometrics with strontium and lead isotope ratios and multielement concentrations.

    PubMed

    Ariyama, Kaoru; Shinozaki, Miyuki; Kawasaki, Akira

    2012-02-22

    The objective of this study was to develop a technique for determining the country of origin of rice in the Japanese market. The rice samples included a total of 350 products grown in Japan (n = 200), the United States (n = 50), China (n = 50), and Thailand (n = 50). In this study, (87)Sr/(86)Sr and Pb isotope ((204)Pb, (206)Pb, (207)Pb, and (208)Pb) ratios and multielement concentrations (Al, Fe, Co, Ni, Cu, Rb, Sr, and Ba) were determined by high-resolution inductively coupled plasma mass spectrometry. By combining three chemometric techniques based on different principles and determination criteria, the countries of origin of rice were determined. The predictions made by 10-fold cross-validation were around 97% accurate. The presented method demonstrated the effectiveness of determining the geographic origin of an agricultural product by combining several chemometric techniques using heavy element isotope ratios and multielement concentrations.

  5. Systematic Study of the {sup 87}Sr Clock Transition in an Optical Lattice

    SciTech Connect

    Ludlow, Andrew D.; Boyd, Martin M.; Zelevinsky, Tanya; Foreman, Seth M.; Blatt, Sebastian; Notcutt, Mark; Ido, Tetsuya; Ye Jun

    2006-01-27

    With ultracold {sup 87}Sr confined in a magic wavelength optical lattice, we present the most precise study (2.8 Hz statistical uncertainty) to date of the {sup 1}S{sub 0}-{sup 3}P{sub 0} optical clock transition with a detailed analysis of systematic shifts (19 Hz uncertainty) in the absolute frequency measurement of 429 228 004 229 869 Hz. The high resolution permits an investigation of the optical lattice motional sideband structure. The local oscillator for this optical atomic clock is a stable diode laser with its hertz-level linewidth characterized by an octave-spanning femtosecond frequency comb.

  6. (86)Y production via (86)Sr(p,n) for PET imaging at a cyclotron.

    PubMed

    Sadeghi, M; Aboudzadeh, M; Zali, A; Zeinali, B

    2009-01-01

    Excitation functions of (86)Y production via (86)Sr(p,xn), (86)Sr(d,xn), (85)Rb(alpha,xn), (85)Rb((3)He,xn), and (nat)Zr(d,alphaxn) reactions were studied by means of ALICE-ASH code and the results were compared with ALICE-91 code and experimental data. The greatest nuclear reaction of cyclotron (86)Y production was found out as (86)Sr(p,n)(86)Y process. (86)Y production yield was calculated too. A SrCO(3) thick film was deposited on a copper substrate by sedimentation method. The deposited (nat)SrCO(3) was irradiated with 15MeV proton at 30microA current beam. The separation of Y from Cu and Sr was carried out by means of dual ion exchange chromatography.

  7. 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

  8. Inelastic collisions and density-dependent excitation suppression in a {sup 87}Sr optical lattice clock

    SciTech Connect

    Bishof, M.; Martin, M. J.; Swallows, M. D.; Benko, C.; Lin, Y.; Quemener, G.; Rey, A. M.; Ye, J.

    2011-11-15

    We observe two-body loss of {sup 3} P{sub 0} {sup 87}Sr atoms trapped in a one-dimensional optical lattice. We measure loss rate coefficients for atomic samples between 1 and 6 {mu}K that are prepared either in a single nuclear-spin sublevel or with equal populations in two sublevels. The measured temperature and nuclear-spin preparation dependence of rate coefficients agree well with calculations and reveal that rate coefficients for distinguishable atoms are only slightly enhanced over those of indistinguishable atoms. We further observe a suppression of excitation and losses during interrogation of the {sup 1} S{sub 0}-{sup 3} P{sub 0} transition as density increases and Rabi frequency decreases, which suggests the presence of strong interactions in our dynamically driven many-body system.

  9. {sup 87}Sr Lattice Clock with Inaccuracy below 10{sup -15}

    SciTech Connect

    Boyd, Martin M.; Ludlow, Andrew D.; Blatt, Sebastian; Foreman, Seth M.; Ido, Tetsuya; Zelevinsky, Tanya; Ye Jun

    2007-02-23

    Aided by ultrahigh resolution spectroscopy, the overall systematic uncertainty of the {sup 1}S{sub 0}-{sup 3}P{sub 0} clock resonance for lattice-confined {sup 87}Sr has been characterized to 9x10{sup -16}. This uncertainty is at a level similar to the Cs-fountain primary standard, while the potential stability for the lattice clocks exceeds that of Cs. The absolute frequency of the clock transition has been measured to be 429 228 004 229 874.0(1.1) Hz, where the 2.5x10{sup -15} fractional uncertainty represents the most accurate measurement of a neutral-atom-based optical transition frequency to date.

  10. Using δ87Sr values to identify sources of salinity to a freshwater aquifer, Greater Aneth Oil Field, Utah, USA

    USGS Publications Warehouse

    Naftz, D.L.; Peterman, Z.E.; Spangler, L.E.

    1997-01-01

    Salinity increases in water from the freshwater Navajo aquifer in the Aneth area have been documented in recent years. Previous studies during the 1980s in the Aneth area suggested that brines associated with oil production and their subsequent re-injection were the probable source of salinity in the Navajo aquifer. Differences in the delta strontium-87 (δ87Sr) composition of ground-water samples from southeastern Utah were used to determine if oil-field brine or water from the upper Paleozoic aquifer is a plausible source of salinity to the Navajo aquifer. The δ87Sr values of the oil-field brine samples (mean = −0.95%, range = −1.06 to −0.79%, n = 5) are substantially more negative than the values in water samples from wells completed in the Navajo aquifer (mean = 0.73, range = −0.85 to 2.02%, n = 48), indicating that oil-field brine is not a source of salinity. The δ87Sr values in water samples from wells completed in the upper Paleozoic aquifer (mean = 0.801% range = 0.34 to 1.10%, n = 4) are similar to the mean isotopic composition of the more saline water from the Navajo aquifer. The δ87Sr values in water from the Navajo aquifer confirm that two distinct flow areas are present. Mixing models using the δ87Sr values and Sr concentrations of non-saline water from the Navajo aquifer and saline water from the upper Paleozoic aquifer indicate that water from the upper Paleozoic aquifer is a plausible source of saline water to the Navajo aquifer. Most Navajo aquifer wells that contain water with a δ87Sr signature similar to water from the upper Paleozoic aquifer are located within or adjacent to an area where the hydraulic gradient is favorable for upward movement of water from the upper Paleozoic aquifer into the Navajo aquifer.

  11. Determination of the source of bioavailable Sr using ⁸⁷Sr/⁸⁶Sr tracers: a case study of hot pepper and rice.

    PubMed

    Song, Byeong-Yeol; Ryu, Jong-Sik; Shin, Hyung Seon; Lee, Kwang-Sik

    2014-09-24

    The geographical origin of agricultural products has been intensively studied, but links between agricultural products and the environments are poorly established. Soils, water (streamwater and groundwater), and plants (hot pepper, Capsicum annuum; and rice, Oryza sativa) were collected from all regions of South Korea and measured Sr isotope ratios ((87)Sr/(86)Sr). Sequential leaching of soil showed that Sr in the exchangeable and carbonate fractions (bioavailable) had a lower (87)Sr/(86)Sr ratio than that in the silicate fraction, consistent with a low (87)Sr/(86)Sr ratio in the plant. Although the bedrock-soil-water-plant system is closely linked, statistical analysis indicated that (87)Sr/(86)Sr ratios of the plant showed the greatest agreement with those of water and the exchangeable fraction of soil. This study is the first report of (87)Sr/(86)Sr isoscapes in South Korea and first demonstrates that the agricultural product is strongly linked with the exchangeable fraction of soil and water.

  12. Carbonate deposition, Pyramid Lake subbasin, Nevada: 3. The use of87Sr values in carbonate deposits (tufas) to determine the hydrologic state of paleolake systems

    USGS Publications Warehouse

    Benson, L.; Peterman, Z.

    1996-01-01

    Sierran rivers that discharge to the Lahontan basin have much lower (???4.5%o) ??87Sr values than the Humboldt River which drains northeastern Nevada. The ??87Sr values of tufas deposited during the last lake cycle were used to determine when Humboldt derived Sr entered the Pyramid Lake subbasin. Prior to ~ 15,000 yr B.P., the Humboldt River flowed to the Smoke Creek-Black Rock Desert subbasin. During the recession of Lake Lahontan, the Humboldt River diverted to the Carson Desert subbasin. This study has demonstrated that 87Sr can be used to determine drainage histories of multi-basin lake systems if the ??87Sr values of rivers that discharge to the basins are sufficiently different. ?? 1995 Elsevier Science B.V. All rights reserved.

  13. 87Sr solid-state NMR as a structurally sensitive tool for the investigation of materials: antiosteoporotic pharmaceuticals and bioactive glasses.

    PubMed

    Bonhomme, Christian; Gervais, Christel; Folliet, Nicolas; Pourpoint, Frédérique; Diogo, Cristina Coelho; Lao, Jonathan; Jallot, Edouard; Lacroix, Joséphine; Nedelec, Jean-Marie; Iuga, Dinu; Hanna, John V; Smith, Mark E; Xiang, Ye; Du, Jincheng; Laurencin, Danielle

    2012-08-01

    Strontium is an element of fundamental importance in biomedical science. Indeed, it has been demonstrated that Sr(2+) ions can promote bone growth and inhibit bone resorption. Thus, the oral administration of Sr-containing medications has been used clinically to prevent osteoporosis, and Sr-containing biomaterials have been developed for implant and tissue engineering applications. The bioavailability of strontium metal cations in the body and their kinetics of release from materials will depend on their local environment. It is thus crucial to be able to characterize, in detail, strontium environments in disordered phases such as bioactive glasses, to understand their structure and rationalize their properties. In this paper, we demonstrate that (87)Sr NMR spectroscopy can serve as a valuable tool of investigation. First, the implementation of high-sensitivity (87)Sr solid-state NMR experiments is presented using (87)Sr-labeled strontium malonate (with DFS (double field sweep), QCPMG (quadrupolar Carr-Purcell-Meiboom-Gill), and WURST (wideband, uniform rate, and smooth truncation) excitation). Then, it is shown that GIPAW DFT (gauge including projector augmented wave density functional theory) calculations can accurately compute (87)Sr NMR parameters. Last and most importantly, (87)Sr NMR is used for the study of a (Ca,Sr)-silicate bioactive glass of limited Sr content (only ~9 wt %). The spectrum is interpreted using structural models of the glass, which are generated through molecular dynamics (MD) simulations and relaxed by DFT, before performing GIPAW calculations of (87)Sr NMR parameters. Finally, changes in the (87)Sr NMR spectrum after immersion of the glass in simulated body fluid (SBF) are reported and discussed.

  14. 87Sr solid-state NMR as a structurally sensitive tool for the investigation of materials: antiosteoporotic pharmaceuticals and bioactive glasses.

    PubMed

    Bonhomme, Christian; Gervais, Christel; Folliet, Nicolas; Pourpoint, Frédérique; Diogo, Cristina Coelho; Lao, Jonathan; Jallot, Edouard; Lacroix, Joséphine; Nedelec, Jean-Marie; Iuga, Dinu; Hanna, John V; Smith, Mark E; Xiang, Ye; Du, Jincheng; Laurencin, Danielle

    2012-08-01

    Strontium is an element of fundamental importance in biomedical science. Indeed, it has been demonstrated that Sr(2+) ions can promote bone growth and inhibit bone resorption. Thus, the oral administration of Sr-containing medications has been used clinically to prevent osteoporosis, and Sr-containing biomaterials have been developed for implant and tissue engineering applications. The bioavailability of strontium metal cations in the body and their kinetics of release from materials will depend on their local environment. It is thus crucial to be able to characterize, in detail, strontium environments in disordered phases such as bioactive glasses, to understand their structure and rationalize their properties. In this paper, we demonstrate that (87)Sr NMR spectroscopy can serve as a valuable tool of investigation. First, the implementation of high-sensitivity (87)Sr solid-state NMR experiments is presented using (87)Sr-labeled strontium malonate (with DFS (double field sweep), QCPMG (quadrupolar Carr-Purcell-Meiboom-Gill), and WURST (wideband, uniform rate, and smooth truncation) excitation). Then, it is shown that GIPAW DFT (gauge including projector augmented wave density functional theory) calculations can accurately compute (87)Sr NMR parameters. Last and most importantly, (87)Sr NMR is used for the study of a (Ca,Sr)-silicate bioactive glass of limited Sr content (only ~9 wt %). The spectrum is interpreted using structural models of the glass, which are generated through molecular dynamics (MD) simulations and relaxed by DFT, before performing GIPAW calculations of (87)Sr NMR parameters. Finally, changes in the (87)Sr NMR spectrum after immersion of the glass in simulated body fluid (SBF) are reported and discussed. PMID:22738329

  15. 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.

  16. 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.

  17. Reconstructing the migration patterns of late Pleistocene mammals from northern Florida, USA

    NASA Astrophysics Data System (ADS)

    Hoppe, Kathryn A.; Koch, Paul L.

    2007-11-01

    We used analyses of the strontium isotope ( 87Sr/ 86Sr) ratios of tooth enamel to reconstruct the migration patterns of fossil mammals collected along the Aucilla River in northern Florida. Specimens date to the late-glacial period and before the last glacial maximum (pre-LGM). Deer and tapir displayed low 87Sr/ 86Sr ratios that were similar to the ratios of Florida environments, which suggest that these taxa did not migrate long distance outside of the Florida region. Mastodons, mammoths, and equids all displayed a wide range of 87Sr/ 86Sr ratios. Some individuals in each taxon displayed low 87Sr/ 86Sr ratios that suggest they ranged locally, while other animals had high 87Sr/ 86Sr ratios that suggest they migrated long distances (> 150 km) outside of the Florida region. Mastodons were the only taxa from this region that provided enough well-dated specimens to compare changes in migration patterns over time. Pre-LGM mastodons displayed significantly lower 87Sr/ 86Sr ratios than late-glacial mastodons, which suggests that late-glacial mastodons from Florida migrated longer distances than their earlier counterparts. This change in movement patterns reflects temporal changes in regional vegetation patterns.

  18. 234U/238U and δ87Sr in peat as tracers of paleosalinity in the Sacramento-San Joaquin Delta of California, USA

    USGS Publications Warehouse

    Drexler, Judith Z.; Paces, James B.; Alpers, Charles N.; Windham-Myers, Lisamarie; Neymark, Leonid; Bullen, Thomas D.; Taylor, Howard E.

    2013-01-01

    The purpose of this study was to determine the history of paleosalinity over the past 6000+ years in the Sacramento-San Joaquin Delta (the Delta), which is the innermost part of the San Francisco Estuary. We used a combination of Sr and U concentrations, d87Sr values, and 234U/238U activity ratios (AR) in peat as proxies for tracking paleosalinity. Peat cores were collected in marshes on Browns Island, Franks Wetland, and Bacon Channel Island in the Delta. Cores were dated using 137Cs, the onset of Pb and Hg contamination from hydraulic gold mining, and 14C. A proof of concept study showed that the dominant emergent macrophyte and major component of peat in the Delta, Schoenoplectus spp., incorporates Sr and U and that the isotopic composition of these elements tracks the ambient water salinity across the Estuary. Concentrations and isotopic compositions of Sr and U in the three main water sources contributing to the Delta (seawater, Sacramento River water, and San Joaquin River water) were used to construct a three-end-member mixing model. Delta paleosalinity was determined by examining variations in the distribution of peat samples through time within the area delineated by the mixing model. The Delta has long been considered a tidal freshwater marsh region, but only peat samples from Franks Wetland and Bacon Channel Island have shown a consistently fresh signal (<0.5 ppt) through time. Therefore, the eastern Delta, which occurs upstream from Bacon Channel Island along the San Joaquin River and its tributaries, has also been fresh for this time period. Over the past 6000+ years, the salinity regime at the western boundary of the Delta (Browns Island) has alternated between fresh and oligohaline (0.5-5 ppt).

  19. Sr-Isotope record of Quaternary marine terraces on the California coast and off Hawaii

    USGS Publications Warehouse

    Ludwig, K. R.; Muhs, D.R.; Simmons, K.R.; Moore, J.G.

    1992-01-01

    Strontium-isotopic ratios of dated corals have been obtained from submerged reefs formed during Quaternary glacial periods off the Hawaiian islands. These data, combined with data from deep-sea sediments, tightly constrain the secular variation of marine 87Sr 86Sr for the past 800,000 yr. Although long-term trends are apparent, no significant (>0.02???), rapid (<100,000 yr) excursions in 87Sr 86Sr were resolved nor did we observe any samples with 87Sr 86Sr greater than that of modern seawater. Strontium in mollusks from elevated marine terraces formed during interglacial periods on the southern California coast show resolvable and consistent variations in 87Sr 86Sr which, when compared to the trend of Quaternary marine 87Sr 86Sr, can be used to infer uplift rates and define approximate ages for the higher terraces. The Sr-isotope age estimates indicate that uplift rates vary among crustal blocks and were not necessarily constant with time. No contrast in Sr-isotopic ratios between similar-age Hawaiian and California fossils was observed, confirming that any change in marine 87Sr 86Sr from glacial to interglacial periods must be small. A realistic appraisal of the potential of Sr-isotope stratigraphy for chronometric applications in the Quaternary suggests that the technique will be limited to relatively coarse distinctions in age. ?? 1992.

  20. Strontium isotopes in otoliths of a non-migratory fish (slimy sculpin): Implications for provenance studies

    USGS Publications Warehouse

    Brennan, Sean R.; Fernandez, Diego P.; Zimmerman, Christian E.; Cerling, Thure E.; Brown, Randy J.; Wooller, Matthew J.

    2015-01-01

    Heterogeneity in 87Sr/86Sr ratios of river-dissolved strontium (Sr) across geologically diverse environments provides a useful tool for investigating provenance, connectivity and movement patterns of various organisms and materials. Evaluation of site-specific 87Sr/86Sr temporal variability throughout study regions is a prerequisite for provenance research, but the dynamics driving temporal variability are generally system-dependent and not accurately predictable. We used the time-keeping properties of otoliths from non-migratory slimy sculpin (Cottus cognatus) to evaluate multi-scale 87Sr/86Sr temporal variability of river waters throughout the Nushagak River, a large (34,700 km2) remote watershed in Alaska, USA. Slimy sculpin otoliths incorporated site-specific temporal variation at sub-annual resolution and were able to record on the order of 0.0001 changes in the 87Sr/86Sr ratio. 87Sr/86Sr profiles of slimy sculpin collected in tributaries and main-stem channels of the upper watershed indicated that these regions were temporally stable, whereas the Lower Nushagak River exhibited some spatio-teporal variability. This study illustrates how the behavioral ecology of a non-migratory organism can be used to evaluate sub-annual 87Sr/86Sr temporal variability and has broad implications for provenance studies employing this tracer.

  1. Stable Strontium (δ88/86Sr) and U-Th isotope systematics of cold-water corals: A combined proxy for Holocene changes of the Mediterranean outflow

    NASA Astrophysics Data System (ADS)

    Liebetrau, V.; Rüggeberg, A.; Fietzke, J.; Eisenhauer, A.; Flögel, S.; Linke, P.; Schönfeld, J.

    2007-12-01

    formation is supported by coincidence of its actual elevated position with the lack of living Lophelia pertusa at the sampling site. The stable strontium isotope ratio δ88/86Sr of biogenic carbonates may serve as a new paleo-temperature proxy for reef-building and solitary deep-sea corals and thus introduce new perspectives in paleoceanography, such as changes in intermediate and deep-sea temperature and ocean circulation. Fietzke J. and Eisenhauer A. (2006), G-cubed 7 Q08009, doi:10.1029/2006GC001243. Schönfeld J. and Zahn R. (2000), Palaeogeography Palaeoclimatology, Palaeoecology 159, 85 - 111.

  2. 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

    2013-09-01

    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.

  3. Rb/Sr isotopic and compositional retentivity of muscovite during deformation

    NASA Astrophysics Data System (ADS)

    Eberlei, T.; Habler, G.; Wegner, W.; Schuster, R.; Körner, W.; Thöni, M.; Abart, R.

    2015-06-01

    Permian metapegmatite muscovite from the Upper-Austroalpine Matsch Unit in Southern Tyrol (Italy) was investigated regarding its Rb/Sr and compositional retentivity during Cretaceous Upper-greenschist facies deformation. The data imply that microstructurally relic Permian magmatic muscovite largely maintained its major and trace element compositions during deformation, whereas the Rb/Sr geochronometer is strongly affected by a net loss of Sr. Lower Sr concentrations of muscovite correlate with higher 87Rb/86Sr and 87Sr/86Sr ratios. In most samples, the muscovite grain size- and magnetic-fractions with the lowest 87Rb/86Sr and 87Sr/86Sr ratios preserve a Permo-Triassic muscovite-whole rock Rb/Sr apparent age interpreted as to reflect formation during or cooling after pegmatite emplacement. Contrastingly, muscovite fractions with higher 87Rb/86Sr and 87Sr/86Sr ratios are arranged along a roughly linear array with a positive correlation of the 87Rb/86Sr and 87Sr/86Sr ratios in the 87Rb/86Sr vs 87Sr/86Sr space. They yield successively lower muscovite-whole rock Rb/Sr apparent ages. We explain the variations in the Rb/Sr isotopic character of microstructurally relic muscovite by a, presumably deformation-related, loss of Sr during the Cretaceous event. Contemporaneously, only very limited amounts of isotopically different Sr from the matrix reservoir might possibly have entered the muscovite. Consequently, the Rb/Sr of the relic muscovite is affected by a net loss of Sr. The results imply that at temperatures of < 500 °C, deformation is supposed to be the predominant factor in controlling the Rb/Sr geochronometer of relic muscovite, by significantly reducing the characteristic length scale for volume diffusion. However, variations of the major and trace element compositions within Permian relic muscovite are interpreted to rather reflect primary compositional instead of deformation-related variations.

  4. 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.

  5. Magma mixing, recharge and eruption histories recorded in plagioclase phenocrysts from El Chichon Volcano, Mexico

    USGS Publications Warehouse

    Tepley, F. J.; Davidson, J.P.; Tilling, R.I.; Arth, Joseph G.

    2000-01-01

    Consistent core-to-rim decreases of 87Sr/86Sr ratios and coincident increases in Sr concentrations in plagioclase phenocrysts of varying size (~ 1 cm to 2 mm) are reported from samples of the 1982 and pre-1982 (~ 200 ka) eruptions of El Chichon Volcano. Maximum 87Sr/86Sr ratios of ~ 0.7054, significantly higher than the whole-rock isotopic ratios (~ 0.7040-0.7045), are found in the cores of plagioclase phenocrysts, and minimum 87Sr/86Sr ratios of ~ 0.7039 are found near some of the rims. Plagioclase phenocrysts commonly display abrupt fluctuations in An content (up to 25 mol %) that correspond to well-developed dissolution surfaces The isotopic, textural and compositional characteristics suggest that these plagioclase phenocrysts grew in a system that was periodically recharged by higher-temperature magma with a lower 87Sr/86Sr ratio and a higher Sr concentration. Rim 87Sr/86Sr ratios in plagioclase phenocrysts of rocks from the 200 ka eruption indicate that, at that time, the magma had already attained the lowest recorded 87Sr/86Sr value of the system (~ 0.7039). In contrast, cores from plagioclase phenocrysts of the 1982 eruption, inferred to have grown in the past few thousand years, have the highest recorded 87Sr/86Sr ratios of the system. Collectively, the Sr isotopic data (for plagioclase and whole rock), disequilibrium textural features of the phenocrysts, known eruption frequencies, and inferred crystal-residence times of the plagioclases are best interpreted in terms of an intermittent magma chamber model. Similar processes, including crustal contamination, magma mixing, periodic recharge by addition of more mafic magma to induce plagioclase disequilibrium (possibly triggering eruption) and subsequent re-equilibration, apparently were operative throughout the 200 ky history of the El Chichon magma system.

  6. Dating the Martian meteorite Zagami by the 87Rb-87Sr isochron method with a prototype in situ resonance ionization mass spectrometer

    PubMed Central

    Scott Anderson, F; Levine, Jonathan; Whitaker, Tom J

    2015-01-01

    RATIONALE The geologic history of the Solar System builds on an extensive record of impact flux models, crater counts, and ∼270 kg of lunar samples analyzed in terrestrial laboratories. However, estimates of impactor flux may be biased by the fact that most of the dated Apollo samples were only tenuously connected to an assumed geologic context. Moreover, uncertainties in the modeled cratering rates are significant enough to lead to estimated errors for dates on Mars and the Moon of ∼1 Ga. Given the great cost of sample return missions, combined with the need to sample multiple terrains on multiple planets, we have developed a prototype instrument that can be used for in situ dating to better constrain the age of planetary samples. METHODS We demonstrate the first use of laser ablation resonance ionization mass spectrometry for 87Rb-87Sr isochron dating of geological specimens. The demands of accuracy and precision have required us to meet challenges including regulation of the ambient temperature, measurement of appropriate backgrounds, sufficient ablation laser intensity, avoidance of the defocusing effect of the plasma created by ablation pulses, and shielding of our detector from atoms and ions of other elements. RESULTS To test whether we could meaningfully date planetary materials, we have analyzed a piece of the Martian meteorite Zagami. In each of four separate measurements we obtained 87Rb-87Sr isochron ages for Zagami consistent with its published age, and, in both of two measurements that reached completion, we obtained better than 200 Ma precision. Combining all our data into a single isochron with 581 spot analyses gives an 87Rb-87Sr age for this specimen of 360 ±90 Ma. CONCLUSIONS Our analyses of the Zagami meteorite represent the first successful application of resonance ionization mass spectrometry to isochron geochronology. Furthermore, the technique is miniaturizable for spaceflight and in situ dating on other planetary bodies. © 2014 The

  7. Sr isotope tracing of multiple water sources in a complex river system, Noteć River, central Poland.

    PubMed

    Zieliński, Mateusz; Dopieralska, Jolanta; Belka, Zdzislaw; Walczak, Aleksandra; Siepak, Marcin; Jakubowicz, Michal

    2016-04-01

    Anthropogenic impact on surface waters and other elements in the environment was investigated in the Noteć River basin in central Poland. The approach was to trace changes in the Sr isotope composition ((87)Sr/(86)Sr) and concentration in space and time. Systematic sampling of the river water shows a very wide range of (87)Sr/(86)Sr ratios, from 0.7089 to 0.7127. This strong variation, however, is restricted to the upper course of the river, whereas the water in the lower course typically shows (87)Sr/(86)Sr values around 0.7104-0.7105. Variations in (87)Sr/(86)Sr are associated with a wide range of Sr concentrations, from 0.14 to 1.32mg/L. We find that strong variations in (87)Sr/(86)Sr and Sr concentrations can be accounted for by mixing of two end-members: 1) atmospheric waters charged with Sr from the near-surface weathering and wash-out of Quaternary glaciogenic deposits, and 2) waters introduced into the river from an open pit lignite mine. The first reservoir is characterized by a low Sr content and high (87)Sr/(86)Sr ratios, whereas mine waters display opposite characteristics. Anthropogenic pollution is also induced by extensive use of fertilizers which constitute the third source of Sr in the environment. The study has an important implication for future archeological studies in the region. It shows that the present-day Sr isotope signatures of river water, flora and fauna cannot be used unambiguously to determine the "baseline" for bioavailable (87)Sr/(86)Sr in the past.

  8. Strontium isotopic compositions of dissolved and suspended loads from the main channel of the Yangtze River.

    PubMed

    Wang, Zhong-Liang; Zhang, Jing; Liu, Cong-Qiang

    2007-10-01

    The concentrations of Sr and (87)Sr/(86)Sr isotopic ratios have been measured in the dissolved loads from the main channel of the Yangtze River. The result shows that the Yangtze River mainstream water has considerably higher Sr concentration (202-330 microg kg(-1)) and slightly lower (87)Sr/(86)Sr ratio (0.7098-0.7108) than the global average runoff values of dissolved Sr (78 microg kg(-1)) and (87)Sr/(86)Sr ratio (0.7119). The (87)Sr/(86)Sr values of 0.7098-0.7108 in river waters result from the intense weathering of carbonate and evaporate rocks that enriched in the Yangtze River drainage basin. The calculated result based on the end-member mixing model shows that about 91% of total dissolved Sr are derived from the weathering of carbonate and evaporate rocks and the other 9% derived from the weathering of silicate rock. The Yangtze River transports about 1.86 x1 0(11)g yr(-1) (2.12 x 10(9)mol yr(-1)) of dissolved Sr annually to the East China Sea, with an average (87)Sr/(86)Sr of 0.7108. The calculated "(87)Sr(excess) flux" of the Yangtze River is about 2.12 x 10(7)mol yr(-1), indicating the important impact on seawater Sr isotope evolution. The measured (87)Sr/(86)Sr ratios of suspended particulate matters in the Yangtze River water ranging from 0.7178 to 0.7252, are about 0.015 higher than that of corresponding dissolved loads, reflecting more important contribution of silicate particles in suspended particulate matters and preferential dissolution of carbonate rocks during basin weathering.

  9. Chondrites - Initial strontium-87/strontium-86 ratios and the early history of the solar system.

    NASA Technical Reports Server (NTRS)

    Wetherill, G. W.; Mark, R.; Lee-Hu, C.

    1973-01-01

    A sodium-poor, calcium-rich inclusion in the carbonaceous chondrite Allende had a Sr-87/Sr-86 ratio at the time of its formation of 0.69880, as low a value as that found in any other meteorite. The higher Sr-87/Sr-86 ratios found in ordinary chondrites indicate that their formation or isotopic equilibration occurred tens of millions of years later.

  10. Integrating 40Ar-39Ar, 87Rb-87Sr and 147Sm-143Nd geochronology of authigenic illite to evaluate tectonic reactivation in an intraplate setting, central Australia

    NASA Astrophysics Data System (ADS)

    Middleton, Alexander W.; Uysal, I. Tonguç; Bryan, Scott E.; Hall, Chris M.; Golding, Suzanne D.

    2014-06-01

    The Warburton-Cooper basins, central Australia, include a multitude of reactivated fracture-fault networks related to a complex, and poorly understood, tectonic evolution. We investigated authigenic illites from a granitic intrusion and sedimentary rocks associated with prominent structural features (Gidgealpa-Merrimelia-Innamincka Ridge and the Nappamerri Trough). These were analysed by 40Ar-39Ar, 87Rb-87Sr and 147Sm-143Nd geochronology to explore the thermal and tectonic histories of central Australian basins. The combined age data provide evidence for three major periods of fault reactivation throughout the Phanerozoic. While Carboniferous (323.3 ± 9.4 Ma) and Late Triassic ages (201.7 ± 9.3 Ma) derive from basin-wide hydrothermal circulation, Cretaceous ages (∼128 to ∼86 Ma) reflect episodic fluid flow events restricted to the synclinal Nappamerri Trough. Such events result from regional extensional tectonism derived from the transferral of far-field stresses to mechanically and thermally weakened regions of the Australian continent. Specifically, Cretaceous ages reflect continent-wide transmission of tensional stress from a >2500 km long rifting event on the eastern (and southern) Australian margin associated with break-up of Gondwana and opening of the Tasman Sea. By integrating 40Ar-39Ar, 87Rb-87Sr and 147Sm-143Nd dating, this study highlights the use of authigenic illite in temporally constraining the tectonic evolution of intracontinental basins that would otherwise remain unknown. Furthermore, combining Sr- and Ar-isotopic systems enables more accurate dating of authigenesis whilst significantly reducing geochemical pitfalls commonly associated with these radioisotopic dating methods.

  11. Geochemical implications from Sr isotopes and K-Ar age determinations for the cook-austral islands chain

    NASA Astrophysics Data System (ADS)

    Matsuda, Jun-Ichi; Notsu, Kenji; Okano, Jun; Yaskawa, Katsumi; Chungue, Leonard

    1984-04-01

    Sr isotopes and K-Ar ages were determined for volcanic rocks from three islands, Samoa, Rarotonga and Rurutu in the Austral-Gilbert-Marshall chain. We have established that Rurutu originated from the same "hot spot" as Tubuai and Raivavae in the Cook-Austral chain as indicated by its 11 m.y. K-Ar age and ( {87Sr }/{86Sr }) ratios. The ( {87Sr }/{86Sr }) ratios for Rurutu, Tubuai and Raivavae lie in the restricted range 0.7026-0.7035. K-Ar ages of all volcanic rocks from Samoa and Rarotonga are all less than 4 m.y. and their ( {87Sr }/{86Sr }) ratios are much higher than those in Rurutu, Tubuai and Raivavae. These findings suggest that Samoa and Rarotonga did not originate in a single hot spot for the Cook-Austral islands.

  12. High initial Sr isotopic ratios and evidence for magma mixing in the Pioneer batholith of southwest Montana

    SciTech Connect

    Arth, J.G.; Zen, E.; Sellers, G.; Hammarstrom, J.

    1986-05-01

    The northeast part of the composite Pioneer batholith of southwest Montana consists of Late Cretaceous calc-alkaline plutons that vary in composition as a function of age, changing from minor hornblende-biotite quartz diorite at about 76 m.y., to a small pluton of hornblende-biotite tonalite at about 74 m.y., to abundant biotite-hornblende granodiorite and biotite granite at about 72 m.y., to some biotite granodiorite and 2-mica granite at 67 to 65 m.y. Initial /sup 87/Sr//sup 86/Sr ratios (SIRs) for the plutons range from 0.7112 to 0.7160. Magmas having a SIR near 0.7112 appear in most episodes of emplacement, whereas those having higher values are restricted to individual episodes. Two granodiorite plutons of 72 m.y. age show a mutual gradational contact, across which the SIR varies over a distance of 7 km from 0.711 to 0.714. The variation is ascribed to mixing between contemporaneous but isotopically distinct granodiorite magmas. The high SIRs of the batholith are interpreted as reflecting partial melting of portions of Precambrian lower crustal lithosphere to produce mafic to intermediate magma. The source may be similar to parts of Proterozoic gneisses now exposed at the surface. Mafic to intermediate magma may have fractionally crystallized at depth and released residual magma episodically to the upper crust over approximately 11 m.y. The high SIR of the Pioneer batholith is broadly similar to that of large parts of the Idaho batholith to the west, but is distinct from the SIR of the Boulder batholith to the northeast. A significant crustal discontinuity may separate the Pioneer-Idaho region from the Boulder region.

  13. Time differences in the formation of meteorites as determined from the ratio of lead-207 to lead-206

    USGS Publications Warehouse

    Tatsumoto, M.; Knight, R.J.; Allegre, C.J.

    1973-01-01

    Measurements of the lead isotopic composition and the uranium, thorium, and lead concentrations in meteorites were made in order to obtain more precise radiometric ages of these members of the solar system. The newly determined value of the lead isotopic composition of Canyon Diablo troilite is as follows: 206Pb/204Pb = 9.307, 207Pb/204Pb = 10.294, and 208Pb/204Pb = 29.476. The leads of Angra dos Reis, Sioux County, and Nuevo Laredo achondrites are very radiogenic, the 206Pb/204Pb values are about 200, and the uranium-thorium-lead systems are nearly concordant. The ages of the meteorites as calculated from a single-stage 207Pb/206Pb isochron based on the newly determined primordial lead value and the newly reported 235U and 238U decay constants, are 4.528 ?? 10 9 years for Sioux County and Nuevo Laredo and 4.555 ?? 10 9 years for Angra dos Reis. When calculated with the uranium decay constants used by Patterson, these ages are 4.593 ?? 109 years and 4.620 ?? 109 years, respectively, and are therefore 40 to 70 ?? 106 years older than the 4.55 ?? 109 years age Patterson reported. The age difference of 27 ?? 106 years between Angra dos Reis and the other two meteorites is compatible with the difference between the initial 87Sr/86Sr ratio of Angra dos Reis and that of seven basaltic achondrites observed by Papanastassiou and Wasserburg. The time difference is also comparable to that determined by 129I-129Xe chronology. The ages of ordinary chondrites (H5 and L6) range from 4.52 to 4.57 ?? 109 years, and, here too, time differences in the formation of the parent bodies or later metamorphic events are indicated. Carbonaceous chondrites (C2 and C3) appear to contain younger lead components.

  14. All-order perturbation calculation of energies, hyperfine constants, multipole polarizabilities, and blackbody radiation shift in {sup 87}Sr{sup +}

    SciTech Connect

    Safronova, U. I.

    2010-08-15

    Excitation energies of the [Kr]ns{sub 1/2}, [Kr]np{sub j}, [Kr]nd{sub j}, and [Kr]nf{sub j} (n{<=}9 and [Kr]=(1s{sup 2}2s{sup 2}2p{sup 6}3s{sup 2}3p{sup 6}3d{sup 10}4s{sup 2}4p{sup 6}) in Sr ii are evaluated. First-order, second-order, third-order, and all-order Coulomb energies and first-order and second-order Coulomb-Breit energies are calculated. Reduced matrix elements, oscillator strengths, transition rates, and lifetimes are determined for the levels up to n=7. Electric-dipole (5s{sub 1/2}-np{sub j}, n=5-26), electric-quadrupole (5s{sub 1/2}-nd{sub j}, n=4-26), and electric-octupole (5s{sub 1/2}-nf{sub j}, n=4-26) matrix elements are calculated to obtain the ground-state E1, E2, and E3 static polarizabilities. Scalar and tensor polarizabilities for the 5p{sub j}-9p{sub j} and 4d{sub j}-8d{sub j} excited states in Sr ii are also calculated. All the above-mentioned matrix elements are determined using the all-order method. We also investigate the hyperfine structure in {sup 87}Sr{sup +}. The hyperfine A values and B values are determined for the first low-lying levels up to n=7. The quadratic Stark effect on hyperfine-structure levels of the {sup 87}Sr{sup +} ground state is investigated. The calculated shift for the (F=5,M=0){r_reversible}(F=4,M=0) transition is found to be 0.120(1) Hz/(kV/cm){sup 2}. These calculations provide a theoretical benchmark for comparison with the experiment and theory. A careful study of uncertainty of our calculations is carried out for the transition-matrix elements, line strengths, transition rates, lifetimes, polarizabilities, and the Stark shift coefficient.

  15. Application of strontium isotopes for tracing landfill leachate plumes in groundwater.

    PubMed

    Vilomet, J D; Angeletti, B; Moustier, S; Ambrosi, J P; Wiesner, M; Bottero, J Y; Chatelet-Snidaro, L

    2001-12-01

    We are evaluating strontium isotopes as alternative tracers of landfill leachate in groundwater. The municipal landfill studied here is located in southeastern France. This landfill has no bottom liner, and wastes are placed directly on the ground. Based on the evaluation of chloride concentration, the plume extends a maximum of 4,600 m. Strontium isotopic composition characterizes two sources: natural groundwater (87Sr/86Sr = 0.708175) and landfill leachate contamination (87Sr/86Sr = 0.708457). The evolution of mixing ratios obtained with strontium reveals a second source of groundwater contamination: fertilizers (87Sr/ 86Sr = 0.707859). These results suggestthat isotopic signatures can be used to provide useful information on sources of groundwater contamination where conventional water quality parameters may yield ambiguous results.

  16. 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.

  17. Simultaneous extension of both basic microstructural components in scleractinian coral skeleton during night and daytime, visualized by in situ 86Sr pulse labeling.

    PubMed

    Domart-Coulon, I; Stolarski, J; Brahmi, C; Gutner-Hoch, E; Janiszewska, K; Shemesh, A; Meibom, A

    2014-01-01

    Using in situ (12 h) pulse-labeling of scleractinian coral aragonitic skeleton with stable 86Sr isotope, the diel pattern of skeletal extension was investigated in the massive Porites lobata species, grown at 5 m depth in the Gulf of Eilat. Several microstructural aspects of coral biomineralization were elucidated, among which the most significant is simultaneous extension of the two basic microstructural components Rapid Accretion Deposits (RAD; also called Centers of Calcification) and Thickening Deposits (TD; also called fibers), both at night and during daytime. Increased thickness of the 86Sr-labeled growth-front in the RADs compared to the adjacent TDs revealed that in this species RADs extend on average twice as fast as TDs. At the level of the individual corallite, skeletal extension is spatially highly heterogeneous, with sporadic slowing or cessation depending on growth directions and skeletal structure morphology. Daytime photosynthesis by symbiotic dinoflagellates is widely acknowledged to substantially increase calcification rates at the colony and the corallite level in reef-building corals. However, in our study, the average night-time extension rate (visualized in three successive 12 h pulses) was similar to the average daytime extension (visualized in the initial 12 h pulse), in all growth directions and skeletal structures. This research provides a platform for further investigations into the temporal calibration of coral skeletal extension via cyclic growth increment deposition, which is a hallmark of coral biomineralization.

  18. Acidification processes and soil leaching influenced by agricultural practices revealed by strontium isotopic ratios

    NASA Astrophysics Data System (ADS)

    Pierson-Wickmann, Anne-Catherine; Aquilina, Luc; Weyer, Christina; Molénat, Jérôme; Lischeid, Gunnar

    2009-08-01

    In natural river systems, the chemical and isotopic composition of stream- and ground waters are mainly controlled by the geology and water-rock interactions. The leaching of major cations from soils has been recognized as a possible consequence of acidic deposition from atmosphere for over 30 years. Moreover, in agricultural areas, the application of physiological acid fertilizers and nitrogen fertilizers in the ammonia form may enhance the cation leaching through the soil profile into ground- and surface waters. This origin of leached cations has been studied on two small and adjacent agricultural catchments in Brittany, western France. The study catchments are drained by two first-order streams, and mainly covered with cambisoils, issued from the alteration and weathering of a granodiorite basement. Precipitations, soil water- and NH 4 acetate-leachates, separated minerals, and stream waters have been investigated. Chemical element ratios, such as Ba/Sr, Na/Sr and Ca/Sr ratios, as well as Sr isotopic ratios are used to constrain the relative contribution from potential sources of stream water elements. Based on Sr isotopic ratio and element concentration, soil water- and NH 4 acetate leaching indicates (1) a dominant manure/slurry contribution in the top soil, representing a cation concentrated pool, with low 87Sr/ 86Sr ratios; (2) in subsoils, mineral dissolution is enhanced by fertilizer application, becoming the unique source of cations in the saprolite. The relatively high weathering rates encountered implies significant sources of cations which are not accessory minerals, but rather plagioclase and biotite dissolution. Stream water has a very different isotopic and chemical composition compared to soil water leaching suggesting that stream water chemistry is dominated by elements issued from mineral and rock weathering. Agriculture, by applications of chemical and organic fertilizers, can influence the export of major base cations, such as Na +. Plagioclase

  19. The IRHUM database - bioavailable strontium isotope ratios of France for geochemical fingerprinting

    NASA Astrophysics Data System (ADS)

    Willmes, Malte; Moffat, Ian; Grün, Rainer; Armstrong, Richard; Kinsley, Les; McMorrow, Linda

    2013-04-01

    Strontium isotope ratios (87Sr/86Sr) are used as a geochemical tracer in a wide range of fields including archaeology, ecology, soil, food and forensic sciences. These applications are based on the principle that strontium isotopic ratios of materials reflect the geological sources of the strontium, which were available during its formation. Geologic regions with distinct strontium isotope ranges, which depend on their age and composition, can be differentiated. A major constraint for current studies is the lack of robust reference maps to evaluate the strontium isotope ratios measured in the samples. The aim of the IRHUM (isotopic reconstruction of human migration) database is to provide a reference map of bioavailable strontium isotope ratios for continental France. The current dataset contains 400 sample locations covering the major geologic units of the Paris and Aquitaine Basin, the Massif Central, and the Pyrenees. At each site soil and plant samples have been collected to cover the whole range of strontium ratios at a specific location. The database is available online at www.rses.anu.edu.au/research-areas/archaeogeochemistry and contains the bioavailable strontium isotope data as well as major and trace element concentrations for soil and plant samples. Strontium isotopes were analysed using a Neptune multi-collector inductively-coupled plasma mass spectrometer (MC-ICP-MS) and elemental concentrations with a Varian Vista Pro Axial ICP-AES (inductively-coupled plasma atomic emission spectrometer). In addition, IRHUM provides spatial context for each sample, including background geology, field observations and soil descriptions. This metadata allows users to evaluate the suitability of a specific data point for their study. The IRHUM database fills an important gap between high resolution studies from specific sites (e.g. archaeological sites), to the very broad geochemical mapping of Europe. Thus it provides an excellent tool to evaluate the regional context

  20. 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.

  1. Interpreting Environmental Change and Nutrient Cycling Using Major Element and Strontium Isotope Ratios in Tree Rings

    NASA Astrophysics Data System (ADS)

    Ash, A. W.; Blum, J. D.; Eagar, C.; Fahey, T. J.

    2003-12-01

    In northeastern US forest ecosystems affected by acid deposition, calcium and other base cations have been leached from the soil exchange complex thereby increasing the possibility that calcium could become a limiting nutrient and negatively affect ecosystem health. Three of the most significant contributions of calcium to the soil exchange complex are atmospheric deposition, silicate mineral weathering, and non-silicate weathering. Strontium isotope and Ca/Sr ratios can be used to identify the relative inputs from these sources and determine whether they have changed over time. Strontium isotopic compositions and Ca/Sr ratios of tree rings hold promise for interpreting and understanding changes in calcium sources and availability in forest ecosystems. However, before tree rings can be used as a reliable archive for environmental perturbations several important issues must be resolved. These include 1) the degree of differential uptake of Ca and Sr by different tree species, and 2) the degree of translocation of Ca and Sr between growth rings. A manipulation experiment at the Hubbard Brook Experimental Forest (HBEF), NH was conducted, in which wollastonite pellets were applied to an experimental watershed. The wollastonite, with Ca/Sr and 87Sr/86Sr ratios distinct from sources to the soil exchange complex, serves as an environmental tracer. By monitoring the uptake of wollastonite into foliage we demonstrate that the degree of fractionation between Ca and Sr is small and that Ca/Sr ratios provide a good monitor of Ca sources to trees. Uptake into roots of selected species suggests there is not significant physiological discrimination against strontium assimilation in favor of calcium. We also explored the degree of mobility of Ca and Sr once it is incorporated into growth increments by determining the presence of the tracer in older growth increments. We developed a multi-step chemical leaching procedure to isolate a reservoir of Ca in wood that represents Ca

  2. From soil to grape and wine: Variation of light and heavy elements isotope ratios.

    PubMed

    Durante, Caterina; Bertacchini, Lucia; Bontempo, Luana; Camin, Federica; Manzini, Daniela; Lambertini, Paolo; Marchetti, Andrea; Paolini, Mauro

    2016-11-01

    In the development of a geographical traceability model, it is necessary to understand if the value of the monitored indicators in a food is correlated to its origin or if it is also influenced by 'external factors' such as those coming from its production. In this study, a deeper investigation of the trend of direct geographical traceability indicators along the winemaking process of two traditional oenological products was carried out. Different processes were monitored, sampling each step of their production (grape juice, intermediate products and wine). The results related to the determinations of δ(18)O, (D/H)I, (D/H)II, δ(13)C, δ(15)N and (87)Sr/(86)Sr have been reported. Furthermore, correspondence with the isotopic values coming from the respective soil and vine-branch samples have been investigated as well, showing the optimal traceability power of the monitored geographical tracers. PMID:27211693

  3. Sr and Nd isotopic variations in ferromanganese crusts from the Central Pacific: Implications for age and source provenance

    USGS Publications Warehouse

    Futa, K.; Peterman, Z.E.; Hein, J.R.

    1988-01-01

    Isotopic analyses of two hydrogenetic ferromanganese (Fe-Mn) crusts from volcanic edifices in the central Pacific Ocean reveal systematic variations in 87Sr 86Sr and 143Nd 144Nd, with both ratios decreasing as a function of depth into the Fe-Mn crusts. Leaching experiments suggest that Sr in the crusts is contained in at least two discrete sites. A loosely bound Sr, dominated by modern marine Sr, is removed by leaching with a 10 percent acetic acid solution. The 87Sr 86Sr ratio of the residue is significantly less than the 87Sr 86Sr ratio of the unleached material. The Sr-isotope ratios of leached samples are compared with the temporal variation in seawater to provide ages for layers within the Fe-Mn crusts. These data suggest that the oldest crust layers began to accrete in the early to middle Miocene. Correlated to the 87Sr 86Sr variations, 143Nd 144Nd ratios suggest that the Nd-isotope composition of central Pacific Ocean seawater also changed systematically over this time interval, or that the Fe-Mn crusts simply incorporated Nd from various parts of an isotopieally heterogeneous ocean as the crusts were carried along with the oceanic plate. In contrast to the layered ferromanganese crust, the phosphatized volcaniclastic substrates have Sr and Nd isotope compositions that are consistent with their volcanic origin. ?? 1988.

  4. Species and life-history affects the utility of otolith chemical composition to determine natal stream-of-origin in Pacific salmon

    USGS Publications Warehouse

    Zimmerman, Christian E.; Swanson, Heidi K.; Volk, Eric C.; Kent, Adam J.R.

    2013-01-01

    To test the utility of otolith chemical composition as a tool for determining the natal stream of origin for salmon, we examined water chemistry and otoliths of juvenile and adult Chum Salmon Oncorhynchus keta and Coho Salmon O. kisutch from three watersheds (five rivers) in the Norton Sound region of Alaska. The two species are characterized by different life histories: Coho Salmon rear in freshwater for up to 3 years, whereas Chum Salmon emigrate from freshwater shortly after emergence. We used laser ablation (LA) inductively coupled plasma (ICP) mass spectrometry (MS) to quantify element: Ca ratios for Mg, Mn, Zn, Sr, and Ba, and we used multicollector LA-ICP-MS to determine 87Sr:86Sr ratios in otolith regions corresponding to the period of freshwater residence. Significant differences existed in both water and otolith elemental composition, suggesting that otolith composition could be used to discriminate the natal origin of Coho Salmon and Chum Salmon but only when 87Sr:86Sr ratios were included in the discriminant function analyses. The best discriminant model included 87Sr:86Sr ratios, and without 87Sr:86Sr ratios it was difficult to discriminate among watersheds and rivers. Classification accuracy was 80% for Coho Salmon and 68% for Chum Salmon, indicating that this method does not provide sufficient sensitivity to estimate straying rates of Pacific salmon at the scale we studied.

  5. Strontium distribution and origins in a natural clayey formation (Callovian-Oxfordian, Paris Basin, France): A new sequential extraction procedure

    NASA Astrophysics Data System (ADS)

    Lerouge, C.; Gaucher, E. C.; Tournassat, C.; Negrel, P.; Crouzet, C.; Guerrot, C.; Gautier, A.; Michel, P.; Vinsot, A.; Buschaert, S.

    2010-05-01

    Strontium is a good monitor of geochemical processes in natural clayey formations. In the Callovian-Oxfordian formation of Bure in France, strontium is sorbed on clay minerals and carried by carbonates, detrital minerals and accessory celestite. In order to determine the strontium distribution among these different phases, four-step sequential extractions (1. cobalt hexamine trichloride, 2. acetic acid, 3. EDTA and 4. tri-acid) were performed on samples from different levels of the clayey formation. The leachates were also analyzed for strontium isotopes, in order to determine the strontium origins. This sequential procedure is well suited to determining strontium distribution in claystones, although it is less efficient in clay-rich limestones and in celestite-rich samples. The carbonates (38-47% of the total strontium) show 87Sr/ 86Sr ratios (0.7070-0.7071) that have recorded the isotopic composition of the Callovian-Oxfordian seawater. Diagenetic carbonates (dolomite, ankerite and siderite) have almost not incorporated any strontium, which has been trapped by celestite during the late diagenesis. The major part of the celestite shows 87Sr/ 86Sr ratios (0.7069-0.7070) quite close to the primary carbonates. However, a second generation of celestite (0.7074) shows a slight 87Sr-enrichment and is isotopically in equilibrium with the exchangeable strontium (27-48% of the total strontium with a mean 87Sr/ 86Sr value of 0.70745) and the present-day porewater (0.7074). This very low 87Sr-enrichment could be explained by the partial destabilisation of detrital minerals (feldspars, micas, clays) which exhibit 87Sr/ 86Sr ratios consistent with their pristine Hercynian origin (0.7229-0.7350). Diffusion of strontium from the subjacent Dogger aquifers (0.7076-0.7082) could also be invoked to explain the slight 87Sr-enrichment.

  6. Visit the journal at http://www.elsevier.nl/locate/jnlnr/00212 Geologic control of Sr and major element chemistry in Himalayan Rivers, Nepal

    NASA Astrophysics Data System (ADS)

    English, N. B.; Quade, J.; DeCelles, P. G.; Garzione, C. N.

    2000-08-01

    Our study of the Seti River in far western Nepal shows that the solute chemistry of the river and its tributaries is strongly controlled by geology. The Seti flows through four distinct terranes, starting with the Tethyan sedimentary series (TSS) and Greater Himalayan series (GHS). TSS/GHS waters display 87Sr/ 86Sr ratios of <0.73 and high Sr and Ca, consistent with the composition of limestone and marble common in these terranes. The 87Sr/ 86Sr ratio and Mg increase markedly as the river passes into the Lesser Himalayan series (LHS), where tributaries have 87Sr/ 86Sr ratios from 0.75 to 1.02 and high Sr, Ca, and Mg. The high Mg in LHS waters correlate with high 87Sr/ 86Sr ratios, which we attribute to weathering of highly radiogenic (0.71-0.82) dolostones. Tributaries to the Seti River draining the largely carbonate-free Dadeldhura thrust sheet (DTS) have ratios near 0.74, but low Sr, Ca, and Mg and therefore have little impact on Seti mainstem chemistry. Mass balance calculations and CaMg-weathering indices show that carbonate weathering accounts for >70% of total dissolved solids to the Seti River. Sr/Ca ratios of river waters provide a minimum estimate of the %-carbonate weathering contribution to Sr, due to partitioning of Sr and Ca during incongruent dissolution and reprecipitation of calcite. Overall, we attribute high 87Sr/ 86Sr ratios in the Seti River and its tributaries to the weathering of metacarbonates (especially dolostones in the upper Nawakhot Group) which have exchanged Sr with silicates during metamorphism. Our modeling of Sr fluxes in the Seti River indicates that the TSS/GHS accounts for 36-39% of the Sr, the LHS for 40-53%, and 8-23% for the DTS. Prior to exposure of LHS rocks at ˜12 Ma, TSS and GHS carbonates with low 87Sr/ 86Sr ratios dominated Himalayan rivers. We attribute the elevated 87Sr/ 86Sr ratios of Himalayan paleorivers during the late Miocene and Pliocene to exposure and weathering of LHS metacarbonates.

  7. Three-dimensional superconducting behavior and thermodynamic parameters of HgBa{sub 2}Ca{sub 0.86}Sr{sub 0.14}Cu{sub 2}O{sub 6{minus}{delta}}

    SciTech Connect

    Kim, M. |; Lee, S.; Yu, S.; Hur, N.H.

    1996-04-01

    This study measures the temperature dependence of reversible magnetization of grain-aligned HgBa{sub 2}Ca{sub 0.86}Sr{sub 0.14}Cu{sub 2}O{sub 6{minus}{delta}} high-{ital T}{sub {ital c}} superconductor with external magnetic fields parallel to the {ital c} axis. The magnetization is field independent at {ital T}{sup {asterisk}} = 114.5 K, which indicates strong thermal vortex fluctuations. From the vortex fluctuation model, the lower limit of coherence length along the {ital c} axis {xi}{sub {ital c}}(0){approx_equal} 2 and the anisotropy ratio {gamma}{le} 7.7 has been obtained, which implies that this sample is anisotropic three-dimensional (3D) superconductor as Y{sub 1}Ba{sub 2}Cu{sub 3}O{sub 7{minus}{delta}}. These results are supported by good 3D scaling behavior of high-field magnetization around {ital T}{sub {ital c}}({ital H}) as a function of [{ital T}{minus}{ital T}{sub {ital c}}({ital H})]/({ital TH}){sup 2/3}. The thermodynamic critical field {ital H}{sub {ital c}}({ital T}) and the Ginzburg-Landau parameter {kappa} = 114.8 were extracted from the model of Hao {ital et} {ital al}. Also, the various thermodynamic parameters were obtained: the penetration depth {lambda}{sub {ital ab}}(0) = 1913 A, coherence length {xi}{sub {ital ab}}(0) = 13.9 A, and the zero temperature upper critical field {ital H}{sub {ital c}2}(0) = 170.4 T. {copyright} {ital 1996 The American Physical Society.}

  8. 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.

  9. Late Cretaceous base level lowering in Campanian and Maastrichtian depositional sequences, Kure Beach, North Carolina

    USGS Publications Warehouse

    Harris, W.B.; ,

    2006-01-01

    Campanian through Maastrichtian mixed carbonate and siliciclastic sediments in a 422 m continuous core drilled at Kure Beach, NC provide a record of sea-level change. Based on lithology and stratigraphy, depositional sequences are defined, and calcareous nannofossil zones and 87Sr/86Sr ratios and corresponding ages using the LOWESS Table determined. Campanian and Maastrichtian sediments comprise six depositional sequences. The oldest is Tar Heel 1 and contains calcareous nannofossils that indicate assignment to the upper part of Zones CC18a, CC18c and the lower part of CC19. 87Sr/86 Sr ratios indicate ages from 83.2 to 80.0 Ma or lower Campanian. Tar Heel II contains calcareous nannofossils that indicate assignment to the upper part of Zone CC 19 and CC20. 87Sr/86Sr ratios indicate ages from 78.0 to 76.3 Ma or middle Campanian. Donoho Creek I and II are thin and contain calcareous nannofossils referable to upper Zone CC21 and Zone CC22, and to CC23, respectively. The top of Donoho Creek II marks the Campanian-Maastrichtian boundary. Donoho Creek I 87Sr/86Sr ratios cluster into two groups, and provide ages from 78.0 to 76.2 Ma and 73.7 to 72.3 Ma, respectively. 87Sr/86Sr ratios in Donoho Creek II indicate ages from 71.4 to 69.6 Ma. Two Maastrichtian sequences are present; the lowermost Peedee I contains calcareous nannofossils that place it in Zones CC25a and CC25b. 87Sr/86Sr r ratios indicate an age from 69.3 to 66.9 Ma or late Maastrichtian. Peedee II is assigned to calcareous nannofossil Zone CC26a. 87Sr/86Sr ratios indicate ages from 66.4 to 65.2 Ma or late Maastrichtian. The four Campanian sequences correlate to three depositional sequences in New Jersey; the sequence boundary between upper Campanian Donoho Creek I and Donoho Creek II is not recognized in New Jersey. This boundary is interpreted to result from Gulf Stream impingement and subsequent erosion on the outer shelf. The two Maastrichtian sequences recognized in the Kure Beach core correlate to the two

  10. Orphan strontium-87 in abyssal peridotites: daddy was a granite.

    PubMed

    Snow, J E; Hart, S R; Dick, H J

    1993-12-17

    The (87)Sr/(86)Sr ratios in some bulk abyssal and alpine peridotites are too high to be binary mixtures of depleted mantle and seawater components. The apparent excess, or "orphan," (87)Sr appears to be separated from its radioactive parent. Such observations were widely held to be analytical artifacts. Study of several occurrences of orphan (87)Sr shows that the orphan component in abyssal peridotite is located in the alteration products of olivine and enstatite in the peridotite. The orphan (87)Sr is most likely introduced by infiltration of low-temperature (<200 degrees C) seawater bearing suspended detrital particulates. These particulates include grains of detrital clay that are partly derived from continental (that is, granitic) sources and thus are highly radiogenic. Orphan (87)Sr and other radiogenic isotopes may provide a tracer for low-temperature seawater penetrating into the oceanic crust. PMID:17829634

  11. Orphan strontium-87 in abyssal peridotites: daddy was a granite.

    PubMed

    Snow, J E; Hart, S R; Dick, H J

    1993-12-17

    The (87)Sr/(86)Sr ratios in some bulk abyssal and alpine peridotites are too high to be binary mixtures of depleted mantle and seawater components. The apparent excess, or "orphan," (87)Sr appears to be separated from its radioactive parent. Such observations were widely held to be analytical artifacts. Study of several occurrences of orphan (87)Sr shows that the orphan component in abyssal peridotite is located in the alteration products of olivine and enstatite in the peridotite. The orphan (87)Sr is most likely introduced by infiltration of low-temperature (<200 degrees C) seawater bearing suspended detrital particulates. These particulates include grains of detrital clay that are partly derived from continental (that is, granitic) sources and thus are highly radiogenic. Orphan (87)Sr and other radiogenic isotopes may provide a tracer for low-temperature seawater penetrating into the oceanic crust.

  12. U and Sr Isotope Tracers of Agricultural Salinity Sources to the Lower Rio Grande River

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

    Elevated salinity of the lower Rio Grande River deteriorates water quality and limits domestic and agricultural water use. Both natural and anthropogenic processes contribute salts in the Rio Grande. Previous studies have focused on natural salt contributions with less emphasis on anthropogenic sources of salinity in the Rio Grande. Using (234U/238U) activity ratios (UAR), 87Sr/86Sr isotope ratios, and major element concentrations, we aim to trace and quantify the salt loads in the Lower Rio Grande watershed which is greatly impacted by agricultural activities. Between 2009 and 2010, we sampled the Rio Grande stretch and irrigation return flows between the Elephant Butte Reservoir, New Mexico and El Paso, Texas. Furthermore, we monitored in monthly intervals the temporal changes of chemical and isotopic compositions of the Rio Grande at Canutillo, Tx. Our results show higher U and Sr fluxes in the Rio Grande during the irrigation season as compared to the non-irrigation season. The UAR (1.62 to 2.13) and 87Sr/86Sr ratios (0.7099 to 0.7138) were higher in the non-irrigation season compared to the irrigation season (UAR: 1.69 to 1.77; 87Sr/86Sr: 0.7100 to 0.7106). These variations of UAR and 87Sr/86Sr ratios imply multiple sources of U and Sr in the Rio Grande. In contrast, the agricultural return flows show a narrow range of UAR (1.31 to 1.37) and 87Sr/86Sr ratios (0.7091 to 0.7099) in the studied seasons. This is consistent with salinity contributions from agricultural sources. Rio Grande at Canutillo shows low UAR (1.62 to 1.77) and 87Sr/86Sr ratios (0.7104 to 0.7105) during the irrigation season as compared to the non-irrigation season (UAR: 2.04 to 2.24; 87Sr/86Sr: 0.7105 to 0.7109). The low U and Sr signature at Canutillo during the irrigation season is close to that of the agricultural return flows, indicative of agricultural salinity sources. These results provide useful elemental and isotopic constraints for future mass balance calculations of salinity

  13. Design and Application of a Sr-84/Sr-87-Double Spike to Determine Natural Strontium Isotope Fractionation in Carbonates and Silicates

    NASA Astrophysics Data System (ADS)

    Krabbenhoeft, A.; Eisenhauer, A.; Liebetrau, V.; Fietzke, J.; Boehm, F.

    2008-12-01

    In order to precisely determine 88Sr/86Sr- and 87Sr/86Sr-isotope variations in natural samples using TIMS-technique we developed a mixed 87Sr/84Sr-double spike from two solutions enriched in 84Sr and 87Sr, respectively. After mixing the two solutions the Sr-spike ratios have precisely been determined by calibration to the NBS 987 standard. For the determination of natural 88Sr/86Sr- and 87Sr/86Sr-isotope variations in carbonates and silicates two TIMS measurements are required: an unspiked and a spiked run where the Sr-isotope ratios are arbitrarily normalized to a fixed Sr isotope ratio (e.g. mean of the first block). For denormalization and data reduction we adopted the algorithm for Ca isotope measurements (1) presented earlier by Heuser et al.(2003) modified for Sr-isotope measurements. It was found that best results can be achieved if the 84Srspike/84Srsample ratio is higher than about 12. The algorithm allows the simultaneous calculation of 87Sr/86Sr and 88Sr/86Sr ratios. Standard measurements showed a δ88/86Sr-value (δ88/86Sr=((88Sr/86Sr)Sample/(88Sr/86Sr)NBS 987)-1)*1000) of 0.39 for the IAPSO seawater standard corresponding to an external reproducibility of ±0.02 (n=12). The IAPSO δ88/86Sr-value corresponds to a 87Sr/86Sr-ratio of 0.709285(6). Both values are in accordance with earlier publications (2) and theoretical predictions based on the δ88/86Sr ratio of seawater and assuming mass-dependent isotope fractionation. Preliminary application of the Sr- double spike to carbonate samples of the Phanerocoic indicate unexpected δ88/86Sr variations in the order of about 0.2 to 0.3 ‰ which indicate varying supply of Sr from isotopically distinctively different sources. Furthermore a direct comparison of double spike TIMS, bracketing standard and laser- ablation MC-ICP-MS (3) results are in agreement and can be used to discuss limitation and perspectives of future Sr isotope measurements. References: 1 Heuser A., Eisenhauer A., Gussone N., Bock B

  14. ({sup 234}U/{sup 238}U) activity ratios in freshwaters as tracers of hydrological processes: The Strengbach watershed (Vosges, France)

    SciTech Connect

    Riotte, J.; Chabaux, F.

    1999-05-01

    ({sup 234}U/{sup 238}U) and {sup 87}Sr/{sup 86}Sr isotopic ratios, as well as major and trace (U, Ba, Sr, Rb) element concentrations were analyzed in dissolved loads of the Strengback stream (Vosges, France) in order to constrain the sources of U isotopes ({sup 234}U--{sup 238}U) to river waters. The variations of the ({sup 234}U/{sup 238}U) activity ratios along the stream indicate a clear dependence between the ({sup 234}U/{sup 238}U) activity ratios of the surface waters and the different types of rocks forming the watershed, with near equilibrium values for the waters draining granites and high ({sup 234}U/{sup 238}U) disequilibria (1.4) for those flowing over carbonates. The high ({sup 234}U/{sup 238}U) disequilibria are related to a supply of {sup 234}U-enriched groundwaters located within the carbonate rocks. The ({sup 234}U/{sup 238}U) activity ratios of the waters at the outlet of the catchment collecting the sources of the stream on the granitic lithology, decrease from 1.02 to 0.96 when the discharge of the stream increases. Such a tendency requires mixing between a water body enriched in {sup 234}U which weathered the granitic bed rock at secular equilibrium, and a water with a ({sup 234}U/{sup 238}U) activity ratio below unity representing a mobilization of U from material that has already been weathered. Comparison of the geochemical characteristics of waters collected during the year and those collected during a flood event, reveals the involvement of two different weathered end-members, depending on the hydrological conditions: during the year, the dissolved U transported by the river originates from bed-rock and deep horizons of the weathering profile, whereas a significant part of U, during the flood event, is supplied by superficial horizons of soils, probably complexes by organic colloids. These results outline the potential of ({sup 234}U/{sup 238}U) activity ratios to investigate hydrological processes and emphasize that their use as tracers

  15. A novel method to develop an otolith microchemistry model to determine striped bass habitat use in the San Francisco Estuary

    SciTech Connect

    Phillis, C C; Ostrach, D J; Gras, M; Yin, Q; Ingram, B L; Zinkl, J G; Weber, P K

    2006-06-14

    Otolith Sr/Ca has become a popular tool for hind casting habitat utilization and migration histories of euryhaline fish. It can readily identify habitat shifts of diadromous fish in most systems. Inferring movements of fish within estuarine habitat, however, requires a model of that accounts of the local water chemistry and the response of individual species to that water chemistry, which is poorly understood. Modeling is further complicated by the fact that high marine Sr and Ca concentrations results in a rapid, nonlinear increase in water Sr/Ca and {sup 87}Sr/{sup 86}Sr between fresh and marine waters. Here we demonstrate a novel method for developing a salinity-otolith Sr/Ca model for the purpose of reconstructing striped bass (Morone saxatilis) habitat use in the San Francisco Bay estuary. We used correlated Sr/Ca and {sup 87}Sr/{sup 86}Sr ratios measurements from adult otoliths from striped bass that experienced a range of salinities to infer striped bass otolith Sr/Ca response to changes in salinity and water Sr/Ca ratio. Otolith {sup 87}Sr/{sup 86}Sr can be assumed to accurately record water {sup 87}Sr/{sup 86}Sr because there is no biological fractionation of Sr isotopes. Water {sup 87}Sr/{sup 86}Sr can in turn be used to estimate water salinity based on the mixing of fresh and marine water with known {sup 87}Sr/{sup 86}Sr ratios. The relationship between adjacent analyses on otoliths of Sr/Ca and {sup 87}Sr/{sup 86}Sr by LA-ICP-MS and MC-ICP-MS (r{sup 2} = 0.65, n = 66) is used to predict water salinity from a measured Sr/Ca ratio. The nature of this non-linear model lends itself well to identifying residence in the Delta and to a lesser extent Suisun Bay, but does not do well locating residence within the more saline bays west of Carquinez Strait. An increase in the number of analyses would improve model confidence, but ultimately the precision of the model is limited by the variability in the response of individual fish to water Sr/Ca.

  16. Observation of the hyperfine structure of the {sup 2}S{sub 1/2}-{sup 2}D{sub 5/2} transition in {sup 87}Sr{sup +}

    SciTech Connect

    Barwood, G.P.; Gao, K.; Gill, P.; Huang, G.; Klein, H.A.

    2003-01-01

    The hyperfine structure of the {sup 2}S{sub 1/2}-{sup 2}D{sub 5/2} quadrupole transition at 674 nm in {sup 87}Sr{sup +} has been observed. The ion was confined in a Paul trap and cooled using laser radiation at 422 and 1092 nm. The quadrupole transition was observed by monitoring quantum jumps in the 422-nm fluorescence. The odd isotope of strontium has 'clock' transitions independent of the first-order Zeeman shift and the {sup 2}D{sub 5/2} state hyperfine structure constants have been determined as A{sub D{sub 5/2}}=2.1743(14) MHz and B{sub D{sub 5/2}}=49.11(6) MHz. Standard uncertainties have been added in parentheses. These values allow the second-order Zeeman shifts to be calculated. The {sup 88}Sr{sup +}-{sup 87}Sr{sup +} isotope shift for the 674-nm quadrupole transition has been measured to be 247.99(4) MHz.

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

    NASA Astrophysics Data System (ADS)

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

    2008-12-01

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

  18. Strontium isotopic evidence for an enriched source for post-subduction volcanic rocks, Dominican Republic

    SciTech Connect

    Wertz, W.K.; Perfit, M.R.; Shuster, R.D.

    1985-01-01

    Later Cenozoic volcanic rocks from the eastern Las Cuevas region (ELCR), Dominican Republic are dominantly shoshonitic and are associated with a series of east-west trending faults. The ELCR rocks are highly enriched in Sr, Ba, and light REE, but contain relatively low amounts of Rb and HFS ions. Several basalts appear to be unfractionated and have Mg-numbers of >75. These transitional to alkalic volcanic rocks are atypical of Caribbean igneous rocks and are more similar to alkaline centers associated with late-stage, island arc volcanism in other regions. Elevated /sup 87/Sr//sup 86/Sr ratios (0.7041-0.7048) are high in comparison to most other igneous rocks from the Caribbean region and indicate that they were derived from a source relatively enriched in LIL and REE in comparison to the sources which gave rise to the majority of Caribbean igneous rocks. /sup 87/Sr//sup 86/Sr values increase linearly with increasing Sr contents, suggesting mixing of sources with relatively low Sr contents and depleted /sup 87/Sr//sup 86/Sr with material that is highly enriched in Sr and with /sup 87/Sr//sup 86/Sr values around 0.706. This enriched component may be a fluid derived from melting/dehydrating subducted oceanic crust and sediment which metasomatically veined the sub-arc mantle. Small degrees of partial melting (<7%) of this source may be responsible for the unusual and enriched chemical composition of the ELCR volcanic rocks.

  19. Marine vs. local control on seawater Nd-isotope ratios at the northwest coast of Africa during the late Cretaceous-early Eocene

    NASA Astrophysics Data System (ADS)

    Kocsis, L.; Gheerbrant, E.; Mouflih, M.; Cappetta, H.; Ulianov, A.; Chiaradia, M.

    2013-12-01

    At the northwest corner of Africa excellent conditions existed for phosphate formation (i.e., stable upwelling system) during the late Cretaceous-early Eocene. This is probably in relation to stable tectonic evolution of shallow epicontinental basins at a passive continental margin and to their paleogeographic situation between the Atlantic and Tethys marine realms. To better comprehend paleoceanic conditions in this area, radiogenic isotope ratios (87Sr/86Sr and 143Nd/144Nd) and trace element compositions of fossil biogenic apatite are investigated from Maastrichtian to Ypresian shallow marine phosphorite deposits in Morocco (Ouled Abdoun and Ganntour Basins). Rare earth elements (REE) distributions in the fossils are compatible with early diagenetic marine pore fluid represented by negative Ce-anomaly and heavy REE enrichment. An overall shift in Ce-anomaly is apparent with gradually lower values in younger fossils along three distinct assemblages that correspond to Maastrichtian, Danian-Thanetian and Ypresian periods. The temporal change can be interpreted as presence of gradually more oxygenated seawater in the basins. Strontium isotopic ratios of the fossils follow the global Sr-evolution curve. However, the latest Cretaceous and the oldest Paleocene fossils yielded slightly higher ratios than the global ocean, which could reflect minor diagenetic alteration. Neodymium isotopic ratios are quite even along the phosphate series with ɛNd(t) values ranges from -6.8 to -5.8. These values are higher than those reported for average North Atlantic deep water and Tethyan seawater (e.g., Stille et al., 1996; Thomas et al., 2003). For the origin of the stable, high 143Nd/144Nd we propose three main hypotheses: (1) contribution of continental Nd-source, (2) locally controlled deep water Nd-isotope ratios near the coast from where upwelling originated in the area and (3) possible surface marine water contribution from the Pacific across the Atlantic. Stille, P., Steinmann

  20. Stratigraphic correlation of Pleistocene California borderland marine carbonate using strontium isotopes

    SciTech Connect

    Capo, R.C. ); Depaolo, D.J. )

    1990-05-01

    High-precision measurements on carbonate sediments have refined the history of the {sup 87}Sr/{sup 86}Sr ratio in Pleistocene seawater and allowed them to construct a standard {sup 87}Sr/{sup 86}Sr vs. age curve, which the authors have applied to stratigraphic correlations in the California Borderland basins. Foraminifera-nannofossil ooze samples from DSDP (Deep Sea Drilling Project) Site 590 in the Tasman Sea (31{degree}S) were analyzed for {sup 87}Sr/{sup 86}Sr to determine the Sr isotopic ratio of ocean water over the past 2.5 m.y. Modeling suggests that changes in river input associated with large variations in global chemical weathering rates are responsible for the observed variations in the {sup 87}Sr/{sup 86}Sr record during the Pliocene-Pleistocene. From 2.4 m.y. to 0.3 m.y., the {sup 87}Sr/{sup 86}Sr ratio of seawater increased rapidly by 14 {times} 10{sup {minus}5}, which makes this period ideal for high-resolution correlations using the Sr isotope method. Based on their standard seawater curve, strontium isotope analyses of macrofossils and foraminifera from carbonate sections from the Santa Barbara-Ventura and Los Angeles basins indicate that the Bathhouse Beach section of the Santa Barbara Formation was deposited between 0.9 and 0.4 m.y. ago, and in part is syndepositional with western portions of the nearly Pliocene-Middle Pleistocene Pico Formation of the Ventura basin, and with the lithologically similar Lomita Marl of the San Pedro Formation at Palos Verdes.

  1. Lower crustal xenoliths, Chinese Peak lava flow, central Sierra Nevada.

    USGS Publications Warehouse

    Dodge, F.C.W.; Calk, L.C.; Kistler, R.W.

    1986-01-01

    This assemblage of pyroxenite, peridotite and mafic granulite xenoliths in the toe of a 10 m.y. trachybasalt flow remnant overlying late Cretaceous granitic rocks, indicates the presence of a mafic-ultramafic complex beneath this part of central California; orthopyroxenites, websterites and clinopyroxenites are dominant. A few of the xenoliths contain ovoid opaque patches that are apparently pseudomorphs after garnet and have pyralspite garnet compositions; using a garnet-orthopyroxene geobarometer, they indicate a lower crustal depth of approx 40 km. Abundant mafic granulites can be subdivided into those with Al2O3 = or 15% and showing considerable scatter on oxide variation diagrams. The high-alumina granulite xenoliths have relatively low 87Rb/86Sr but high 87Sr/86Sr, whereas the low-alumina and ultramafic xenoliths have a wide range of 87Rb/86Sr, but lower 87Sr/86Sr; the isotopic data indicate roughly the same age as that of overlying granitic plutons (approx 100 m.y.). However, the granitic rocks have initial 87Sr/86Sr ratios intermediate between those of the high-alumina and ultramafic xenoliths, suggesting that they result from the mixing of basaltic magma (represented by the ultramafic rocks) and crustal materials, with subsequent crystal fractionation.-R.A.H.

  2. The Bagni di Lucca thermal waters (Tuscany, Italy): an example of Ca-SO 4 waters with high Na/Cl and low Ca/SO 4 ratios

    NASA Astrophysics Data System (ADS)

    Boschetti, Tiziano; Venturelli, Giampiero; Toscani, Lorenzo; Barbieri, Maurizio; Mucchino, Claudio

    2005-06-01

    The Bagni di Lucca thermal waters (Lucca province, Tuscany, Italy) have been well known since the Middle Age for their alleged curative properties. In the present work, the waters have been analysed for major and trace components and for O, H, S and Sr isotopes. The δ 2H and δ 18O values indicate a meteoric origin of the waters and the tritium content suggests long-term (more than 40 years) circulation at depth. The δ 34S values in dissolved sulphate of the warmest waters (Doccione, Paolina, Bernabò, Demidoff, Cova) indicate interaction with Triassic evaporites; however, the δ 34S values as well as the 87Sr/ 86Sr ratios in the waters appear to be a little higher (on average 17.6±0.4‰ and 0.70834±0.00006, respectively) than in Triassic sulphate minerals from the Northern Apennines (16.0±0.5‰ and 0.70778±0.00011). The waters are Ca-sulphate and characterised by high Na/Cl (≌2) and low Ca/SO 4 (≌0.7) mole ratios, high Sr (≤12 mg/L), F (≤4.2 mg/L), As (≤80 μg/L), Cs (≤70 μg/L), Rb (≤107 μg/L) and salinity (up to 3087 mg/L of total dissolved solids), low alkalinity, and pH in the range 6.3-7.5. Assuming equilibrium of the waters with anhydrite and chalcedony, the evaluated temperature and pressure are about 70-75 °C and 200-300 bar; considering the pressure as hydrostatic, the evaluated depth of equilibration approaches that of the metamorphic basement (about 3.0-3.8 km) underlying the carbonate-evaporite formations occurring in the area. Thermodynamic computations indicate that the high Na/Cl ratio and the low Ca/SO 4 ratio in the waters may be due to progressive dissolution of albite, anhydrite, dolomite and carbon dioxide accompanied by calcite precipitation. The linear correlations between the major and trace components, including 2H and 18O, demonstrate that thermal springs undergo dilution by low-salinity shallow waters which are recharged at low elevation.

  3. 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

    2016-08-01

    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.

  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. Radiogenic and stable isotopes of mid-Miocene silicic volcanism in eastern Oregon: Evidence for variable and high Sr / low δ18O domains west of the terrane-cratonic lithosphere transition

    NASA Astrophysics Data System (ADS)

    Jenkins, E. N.; Streck, M. J.; Ramos, F. C.; Bindeman, I. N.

    2013-12-01

    Widespread mid-Miocene rhyolite volcanism of eastern Oregon mostly coeval with flood basalts of the Columbia River Basalt Province allows for mapping crustal domains using radiogenic and stable isotopes. Rhyolites are thought to be derived in large part by partial melting of the crust and thus yield direct information on the composition of the crust. Silicic volcanism is expressed in the form of numerous domes and tuffs exposed over a wide area (~300 km in N-S dimension and ~100 km in E-W dimension) west of the craton boundary, which runs parallel but mostly east of the Oregon-Idaho state border as delineated by geophysical characteristics and isotopic transitions. Here, we mainly focus on initial 87Sr/86Sr ratios and δ18O obtained from mid-Miocene silicic volcanic centers in eastern Oregon. Our data, in combination with data from the literature, indicate variable 87Sr/86Sr mostly along longitudinal sections, yet more similar ratios in latitudinal directions. Except for rare examples on the west side, dispersion of 87Sr/86Sr ratios among both silicic and basaltic rocks occurs eastward of 118.6°W. For example, rhyolites in the Owyhee region between 117.10°W and 117.25°W retain 87Sr/86Sr ratios ranging from 0.70413 to 0.70566. The most radiogenic Sri ratio of 0.70787 in our study is obtained on a plagioclase separate from Buchanan Dome complex located near the western boundary of our study area. Feldspar separates and fresh groundmass of samples from adjacent centers yield similar 87Sr/86Sr ratios. δ18O values for feldspars range from below 2‰ to above 9‰. In addition, there is a crude trend of rhyolites having lower δ18O and more radiogenic 87Sr/86Sr ratios. With one exception, all samples with 87Sr/86Sr above 0.7050 are depleted in 18O (δ18O <5.5‰), while rhyolites with 87Sr/86Sr below 0.7045 are enriched in 18O (δ18O >6‰). The most depleted oxygen ratios (<2‰) come from rhyolites ~80 km west of the cratonic margin reflecting remelting or

  6. Strontium isotopic geochemistry of the volcanic rocks and associated megacrysts and inclusions from Ross Island and vicinity, Antarctica

    USGS Publications Warehouse

    Stuckless, J.S.; Ericksen, R.L.

    1976-01-01

    Twelve whole-rock samples of volcanic rocks and a composite of 11 basanitoid samples from Ross Island and vicinity, Antarctica show a narrow range of 87Sr/86Sr ratios from 0.70305 to 0.70339. This range is consistent with a model of differentiation from a single parent magma, but the data allow a 30% variation in the 87Rb/86Sr ratio in the source region if the average ratio is less than 0.057 and if the source region has existed as a closed system for 1.5 b.y. Megacrysts of titaniferous augite, kaersutite, and anorthoclase are isotopically indistinguishable from the host volcanic rocks and therefore are probably cogenetic with the volcanic sequence. A single trachyte sample is isotopically distinct from the rest of the volcanic rocks and probably was contaminated with crustal strontium. Ultramafic and mafic nodules found in association with basanitoids and trachybasalts have 87Sr/86Sr ratios ranging from 0.70275 to 0.70575. Several of these nodules exhibit evidence of reaction with the melt and are isotopically indistinguishable from their hosts, but data for seven granulite-facies nodules show an apparent isochronal relationship. Although this isochron may be fortuitous, the resulting age of 158??22 m.y. is similar to ages reported for the voluminous Ferrar Dolerites, and suggests isotopic re-equilibration within the lower crust and upper mantle. These nodules are not genetically related to the Ferrar Dolerites, as evidenced by their lower initial 87Sr/86Sr ratios. Three ultramafic nodules are texturally and isotopically distinct from the rest of the analyzed nodules. These are friable, have larger 87Sr/86Sr ratios, and may represent a deeper sampling of mantle rock than the granulite-facies nodules. They were, however, derived at a shallower depth than the alkalic magma. Thus they are not genetically related to either the magma or the granulite-facies nodules. ?? 1976 Springer-Verlag.

  7. Strontium isotope variation in the dissolved load and suspended sediments of Northern Hemisphere land terminating glaciers

    NASA Astrophysics Data System (ADS)

    Stevenson, E. I.; Aciego, S.; Arendt, C. A.; Sheik, C.; Das, S. B.

    2014-12-01

    Bedrock, hydrology and microbial communities are primary contributors to sub-glacial chemical weathering and therefore mediate the chemical composition of bulk glacial outflow. Chemical weathering associated with glaciers has attracted attention due to the possible link between increased chemical weathering during glacial retreat and control of the marine radiogenic strontium (87Sr/86Sr) ratios [1-3]. Here we contrast the differences in strontium isotope (87Sr/86Sr) compositions of the dissolved load (DL) and suspended sediments (SS) from bulk subglacial outflows from three, northern hemisphere ice masses. We sampled from sub-glacial outflows draining geographically and geologically distinct glacial termini from the (1) the South, East and West of the Greenland Ice sheet (GIS), (2) the Juneau Icefield and (3) the Columbia Icefield. The diversity in regional outlet facilitates the comparison of glaciers with differing climate, size, hydrology and bedrock. The magnitude of offset in 87Sr/86Sr ratios between the SS and DL (Δ87/86Sr, ‰, = (87Sr/86SrSS - 87Sr/86SrDL)*1000) varies between -62 to +7 ‰ and shows a positive correlation with pH, regardless of differences in glacier size and bedrock lithology. Here we believe the magnitude of the offset between the DL and SS is due to variations in subglacial weathering environments driven primarily by residence times of both water and sediment within the glacial system, and secondarily by bedrock lithology. The most radiogenic Sr compositions (both DL and SS) are found draining the GIS (up to 87Sr/86Sr = 0.80716) indicating the GIS may have provided a significant source of radiogenic Sr to the oceans during times of deglaciation. [1] Armstrong, R.L., (1971) Nature, v. 230, p. 132-133 [2] Capo, R.C., De Paolo, D.J., (1990) Science, v. 249, no. 4964, p. 51-55. [3] Vance, D., Teagle, D.A.H., Foster, G.L. (2009), Nature, v. 458 p. 493-496.

  8. Strontium isotopic variations of Neoproterozoic seawater: Implications for crustal evolution

    SciTech Connect

    Asmerom, Y.; Jacobsen, S.B.; Knoll, A.H.; Butterfield, N.J. ); Swett, K. )

    1991-10-01

    The authors report high precision Sr isotopic data on carbonates from the Neoproterozoic Shaler Group, Victoria Island, Northwest Territories, Canada. Samples with low {sup 87}Rb/{sup 86}Sr ratios (<0.01) were selected for Sr isotopic analysis. {delta}{sup 18}O, Mn, Ca, Mg, and Sr data were used to recognize altered samples. The altered samples are characterized by high Mn/Sr ({ge}2) and variable {delta}{sup 18}O; most are dolomites. The data indicate that between ca. 790-850 Ma the {sup 87}Sr/{sup 86}Sr ratio of seawater varied between 0.70676 and 0.70561. The samples show smooth and systematic variation, with the lowest {sup 87}Sr/{sup 86}Sr value of 0.70561 at ca. 830 Ma. The low {sup 87}Sr/{sup 86}Sr ratio of carbonates from the lower parts of the section is similar to a value reported for one sample from the Adrar of Mauritania ({approx}900 Ma), West African Craton. Isotopic ratios from the upper part of the Shaler section are identical to values from the lower part of the Neoproterozoic Akademikerbreen Group, Spitsbergen. Although a paucity of absolute age determinations hinders attempts at the precise correlation of Neoproterozoic successions, it is possible to draw a broad outline of the Sr isotopic composition of seawater for this period. Data from this study and the literature are used to construct a curve of the {sup 87}Sr/{sup 86}Sr ratio of Neoproterozoic seawater. The Sr isotope composition of seawater reflects primarily the balance between continental Sr input through river input and mantle input via hydrothermal circulation of seawater through mid-ocean ridges. Coupling of Nd and Sr isotopic systems allows the authors to model changes in seafloor spreading rates (or hydrothermal flux) and continental erosion. The Sr hydrothermal flux and the erosion rate (relative to present-day value) are modeled for the period 500-900 Ma.

  9. Isotopic investigations for the origin of relic from the Matsusaki site, Japan.

    PubMed

    Nakano-Ohta, T; Kubota, T; Ando, A; Fujii, T; Fukutani, S; Nakata, E; Nakano, T; Mahara, Y

    2009-01-01

    We measured the environmental radioactivity and isotope ratio, (87)Sr/(86)Sr ratio, (234)U/(238)U, delta(13)C, and (228)Ra/(226)Ra activity ratio, of adhesion that adhered to a wooden tubing vessel obtained from the Matsusaki site, one of the salt-production sites where Moshio is manufactured, in Aichi Prefecture, Japan. The environmental radioactivity and isotope ratio verified that the adhesion originated from the seaweed and/or sea grass.

  10. Application of strontium isotope measurements to trace sediment sources in an upstream agricultural catchment (Loire River basin, France)

    NASA Astrophysics Data System (ADS)

    Le Gall, Marion; Evrard, Olivier; Thil, François; Foucher, Anthony; Salvador-Blanes, Sébastien; Cerdan, Olivier; Ayrault, Sophie

    2015-04-01

    Soil erosion is recognized as one of the main processes of land degradation in agricultural areas. It accelerates the supply of sediment to the rivers and degrades water quality. To limit those impacts and optimize management programs in such areas, sources of sediment need to be identified and sediment transport to be controlled. Here, we determined the sources of suspended sediment in the Louroux (24 km², French Loire River basin), a small catchment representative of lowland cultivated environments of Northwestern Europe. In this catchment, channels have been reshaped and 220 tile drain outlets have been installed over the last several decades. As a result, soil erosion and sediment fluxes have increased drastically. The variation of 87Sr/86Sr ratios, driven by the weathering of rocks with different ages and chemical composition, may reflect the mixing of different sediment sources. Strontium isotopic ratios (87Sr/86Sr) were therefore determined in potential soil sources, suspended particulate matter (SPM) and a sediment core sampled in the Louroux Pond at the catchment outlet. Soil, SPM and core samples displayed significantly different isotopic signatures. 87Sr/86Sr ratios in soil samples varied from 0.712763 to 0.724631 ± 0.000017 (2σ, n=20). Highest values were observed in silicic parts of the catchment whereas the lower values were identified in a calcareous area close to the Louroux Pond. 87Sr/86Sr ratios in SPM (0.713660 to 0.725749 ± 0.000017, 2σ, n=20) plotted between the soil and sediment core (0.712255 to 0.716415 ± 0.000017, 2σ, n=12), suggesting the presence of particles originating from at least two different lithological sources, i.e. silicic rocks and carbonate material. Variations in 87Sr/86Sr ratios in the outlet core sample were used to reconstruct the sedimentary dynamics in the catchment during the last decades. These results will guide the future implementation of appropriate management practices aiming to reduce erosion in upstream

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

    USGS Publications Warehouse

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

    2010-01-01

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

  12. Ratio

    NASA Astrophysics Data System (ADS)

    Webster, Nathan A. S.; Pownceby, Mark I.; Madsen, Ian C.; Studer, Andrew J.; Manuel, James R.; Kimpton, Justin A.

    2014-12-01

    Effects of basicity, B (CaO:SiO2 ratio) on the thermal range, concentration, and formation mechanisms of silico-ferrite of calcium and aluminum (SFCA) and SFCA-I iron ore sinter bonding phases have been investigated using an in situ synchrotron X-ray diffraction-based methodology with subsequent Rietveld refinement-based quantitative phase analysis. SFCA and SFCA-I phases are the key bonding materials in iron ore sinter, and improved understanding of the effects of processing parameters such as basicity on their formation and decomposition may assist in improving efficiency of industrial iron ore sintering operations. Increasing basicity significantly increased the thermal range of SFCA-I, from 1363 K to 1533 K (1090 °C to 1260 °C) for a mixture with B = 2.48, to ~1339 K to 1535 K (1066 °C to 1262 °C) for a mixture with B = 3.96, and to ~1323 K to 1593 K (1050 °C to 1320 °C) at B = 4.94. Increasing basicity also increased the amount of SFCA-I formed, from 18 wt pct for the mixture with B = 2.48 to 25 wt pct for the B = 4.94 mixture. Higher basicity of the starting sinter mixture will, therefore, increase the amount of SFCA-I, considered to be more desirable of the two phases. Basicity did not appear to significantly influence the formation mechanism of SFCA-I. It did, however, affect the formation mechanism of SFCA, with the decomposition of SFCA-I coinciding with the formation of a significant amount of additional SFCA in the B = 2.48 and 3.96 mixtures but only a minor amount in the highest basicity mixture. In situ neutron diffraction enabled characterization of the behavior of magnetite after melting of SFCA produced a magnetite plus melt phase assemblage.

  13. Abundance of alkali metals, alkaline and rare earths, and strontium-87/ strontium-86 ratios in lunar samples.

    PubMed

    Gast, P W; Hubbard, N J

    1970-01-30

    The variation in trace element abundance patterns indicates that lunar igneous rocks are the product of extensive igneous fractionation. Variations in the Sr(87)/ Sr(86) ratio indicate that these rocks crystallized 3.5+/-0.3 x 10(9) years ago.

  14. A strontium, neodymium and oxygen isotope study of hydrothermal metamorphism and crustal anatexis in the Trois Seigneurs Massif, Pyrenees, France

    NASA Astrophysics Data System (ADS)

    Bickle, M. J.; Wickham, S. M.; Chapman, H. J.; Taylor, H. P.

    1988-12-01

    within the Hercynian crust, both at Trois Seigneurs ( ɛ Nd=-3 to -7) and elsewhere in the Pyrenees; almost all igneous lithologies have depleted-mantle, mid-Proterozoic model ages, consistent with efficient recycling of crustal material following original crustal accretion in this area at about 1600 Ma or earlier. Rb-Sr mineral ages exhibit a complex cooling history reflecting late Hercynian and Mesozoic thermal events. Our results show that profound homogenization of the 87Sr/86Sr and 18O/16O ratios of large volumes of the crust can occur during regional metamorphism and crustal anatexis, particularly in regions undergoing extensional tectonics. Such processes can significantly modify the isotopic compositions of the protoliths of granitic magmas; this may explain why many peraluminous Hercynian granitoids of Western Europe have anomalously low (87Sr/86Sr) initial values compared to their probable sedimentary parent rocks.

  15. A 7500-year strontium isotope record from the northwestern Nile delta (Maryut lagoon, Egypt)

    NASA Astrophysics Data System (ADS)

    Flaux, Clément; Claude, Christelle; Marriner, Nick; Morhange, Christophe

    2013-10-01

    During the Holocene, delta evolution has been collectively mediated by relative sea-level changes, continental hydrology and human impacts. In this paper, we present a strontium isotope record from the Maryut lagoon (northwestern Nile delta) to quantify the interplay between relative sea-level variations and Nile flow changes during the past 7500 years. 87Sr/86Sr stratigraphy allows five hydrological stages to be defined. (1) The marine transgression of the area is dated to ˜7.5 ka cal. BP, with a clear marine 87Sr/86Sr signature (0.70905-0.7091). (2) Between ˜7 and ˜5.5 ka, in the context of the so-called African Humid Period (AHP), freshwater inputs became progressively predominant in the Maryut's hydrology. Deceleration of sea-level rise coupled with high Nile discharge induced coastal progradation which led to the progressive closure of the Maryut lagoon. (3) Between ˜5.5 and ˜3.8 ka, the end of the AHP is translated by a progressive hydrological shift from a Nile-dominated to a marine-dominated lagoon (87Sr/86Sr shifts from 0.70865 to 0.7088 to 0.70905-0.70915). (4) From ˜2.8 to ˜1.7 ka, 87Sr/86Sr ratios shift towards lower values (0.7084). Although this change is not precisely resolved because of a hiatus in the Maryut's sedimentary record, the 87Sr/86Sr transition from sea-like to Nile-dominated values is attributed to irrigation practices since the early Ptolemaic period (i.e. since ˜2.3 ka), including the Alexandria canal which played a key role in isolating the Maryut from the Mediterranean sea. (5) The final phase of the record covers the period between ˜1.7 and ˜0.2 ka. 87Sr/86Sr ratios indicate high freshwater inputs (from 0.7080 to 0.7085), except between 1.2 and 1.1 to ˜0.7 ka, when a Maryut lowstand and seawater intrusion are attested. In modern times, the Nile's coastal lagoons have been increasingly supplied by freshwater linked to the diversion of waters from the two Nile branches into the irrigation system. It is suggested that this

  16. Post-eruptive alteration of silicic ignimbrites and lavas, Gran Canaria, Canary Islands: Strontium, neodymium, lead, and oxygen isotopic evidence

    SciTech Connect

    Cousens, B.L. ); Spera, F.J. ); Dobson, P.F. )

    1993-02-01

    Isotopic analyses of Miocene comenditic, pantelleritic, and trachyphonolitic ignimbrites and lavas from Gran Canaria, Canary Islands, provide evidence for posteruptive mobility of Rb, Sr, and O. Calculated initial [sup 87]Sr/[sup 86]Sr ratios in whole-rock samples from basaltic lavas and feldspar mineral separates from ignimbrites define a magmatic trend in the stratigraphic section, from ratios of 0.70340 at the base of the Mogan Formation to 0.70305 in the lower Fataga Formation. However, calculated apparent initial [sup 87]Sr/[sup 86]Sr ratios in hydrated vitrophyre and devitrified matrix separates range from 0.7035 to 0.7090. [delta][sup 18]O ratios in basalts and feldspars vary little, from +5.7 to +6.1, yet range from +6.5 to +15.0 in the ignimbrite matrices. In contrast to the Sr and O isotope ratios, Pb and Nd isotope ratios are identical within analytical error in feldspars and their silicic ignimbrite matrices. Sequential leaching experiments and the oxygen data suggest that low-temperature, posteruptive interaction with meteoric water, perhaps containing a small seawater component, has modified Rb and Sr concentrations in the matrices, such that calculated apparent initial [sup 87]Sr/[sup 86]Sr ratios are not those of the magmas when they were erupted. Mobilization of Rb and Sr must occur significantly after eurption. Nd and Pb isotope systems appear to be unaffected by this process. Therefore, [sup 87]Sr/[sup 86]Sr ratios determined by whole rock analysis of silicic rocks from hotspot-type oceanic islands are suspect and should not be incorporated into mantle tracer studies, although analysis of phenocrysts may produce useful data. 40 refs., 5 figs., 3 tabs.

  17. 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.

  18. Strontium isotope study, Pine Barrens, Long Island, NY

    SciTech Connect

    Xin, Geng; Hanson, G.N. . Dept. of Earth and Space Sciences)

    1993-03-01

    Twenty-four samples representing precipitation, through-fall, soil water, ground water, vegetation and soil were analyzed for strontium concentration and the [sup 87]Sr/[sup 86]Sr ratio. The Pine Barrens, which consists of forests and dense vegetation, covers approximately 300 square miles of the coastal plain of Long Island, New York. This study estimates the relative importance of atmospheric and weathering inputs of Sr to vegetation in this ecosystem. The values of the [sup 87]Sr/[sup 86]Sr ratios and Sr concentration in the Pine Barrens are shown in the attached figure. Precipitation has Sr isotopic ratios that are close to that of sea water (0.7092). The Sr in through-fall is dominated by the Sr from the canopy foliage. The [sup 87]Sr/[sup 86]Sr ratios of soil water and ground water increase with depth. The Sr isotopic ratio for a composite sample of pine (0.71181) is a mixture of atmosphere Sr and soil or ground waters. The Sr isotopic ratios and concentrations in pine suggest that plants are a major reservoir of Sr in the system.

  19. Geochemistry, strontium isotope data, and potassium-argon ages of the andesite-rhyolite association in the Padang area, West Sumatra

    USGS Publications Warehouse

    Leo, G.W.; Hedge, C.E.; Marvin, R.F.

    1980-01-01

    Quaternary volcanoes in the Padang area on the west coast of Sumatra have produced two-pyroxene, calc-alkaline andesite and volumetrically subordinate rhyolitic and andesitic ash-flow tuffs. A sequence of andesite (pre-caldera), rhyolitic tuff and andesitic tuff, in decreasing order of age, is related to Maninjau caldera. Andesite compositions range from 55.0 to 61.2% SiO2 and from 1.13 to 2.05% K2O. Six K-Ar whole-rock age determinations on andesites show a range of 0.27 ?? 0.12 to 0.83 ?? 0.42 m.y.; a single determination on the rhyolitic ashflow tuff gave 0.28 ?? 0.12 m.y. Eight 57Sr/26Sr ratios on andesites and rhyolite tuff west of the Semangko fault zone are in the range 0.7056 - 0.7066. These ratios are higher than those elsewhere in the Sunda arc but are comparable to the Taupo volcanic zone of New Zealand and calc-alkaline volcanics of continental margins. An 87Sr/86Sr ratio of 0.7048 on G. Sirabungan east of the Semangko fault is similar to an earlier determination on nearby G. Marapi (0.7047), and agrees with 87Sr/86Sr ratios in the rest of the Sunda arc. The reason for this distribution of 87Sr/86Sr ratios is unknown. The high 87Sr/86Sr ratios are tentatively regarded to reflect a crustal source for the andesites, while moderately fractionated REE patterns with pronounced negative Eu anomalies suggest a residue enriched in plagioclase with hornblende and/or pyroxenes. Generation of associated andesite and rhyolite could have been caused by hydrous fractional melting of andesite or volcanogenic sediments under adiabatic decompression. ?? 1980.

  20. 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.

  1. Reactivity of evaporites during burial: An example from the Jurassic of Alabama

    SciTech Connect

    Land, L.S.; Eustice, R.A.; Mack, L.E.

    1995-09-01

    The Jurassic Louann salt was the first significant sedimentary unit to accumulate in the Gulf of Mexico sedimentary basin. Br/Cl and {sup 87}Sr/{sup 86}Sr ratios of halite from a single core into the top of the formation record the evaporation of normal seawater to bittern stage. The bittern zone today consists of intergrown halite and sylvite. The Br and Rb contents of the solid phases, along with {sup 87}Sr/{sup 86}Sr ratios and Rb/Sr systematics, are inconsistent with precipitation of the existing phases from seawater evaporated in Jurassic time. Rather, petrography and fluid inclusion and solid phase chemistry from the bittern zone is consistent with postdepositional water/rock interaction which diagenetically modified a marine bittern assemblage to halite + sylvite. The chemistry of the Br- and Rb-rich saline formation waters characteristic of this area today, likewise, may reflect water/evaporite interaction during burial.

  2. Multiple isotopic components in Quaternary volcanic rocks of the Cascade Arc near Crater lake, Oregon

    USGS Publications Warehouse

    Bacon, C.R.; Gunn, S.H.; Lanphere, M.A.; Wooden, J.L.

    1994-01-01

    Quaternary lavas and pyroclastic rocks of Mount Mazama, Crater lake caldera, and the surrounding area have variable Sr, Nd, and Pb isotopic compositions. High-alumina olivine tholeiites have 87Ar/86Ar ratios of 0.70346-0.70364; basaltic andesite, 0.70349-0.70372; shoshonitic basaltic andesite, 0.70374-0.70388; and andesite, 0.70324-0.70383. Dacites of Mount Mazama have 87Sr/ 86Sr ratios of 0.70348-0.70373. Most rhyodacites converge on 0.7037. Andesitic to mafic-cumulate scoriae of the climatic eruption, and enclaves in pre-climactic rhyodacites, cluster in two groups but show nearly the entire 87Sr/86Sr range of the data set, confirming previously suggested introduction of diverse parental magmas into the growing climactic chamber. Magma evolution is described. -from Authors

  3. Implications of Heterogeneous Sr-Isotopes in Olivines from Samoan Lavas

    NASA Astrophysics Data System (ADS)

    Reinhard, A.; Jackson, M. G.; Harvey, J.

    2015-12-01

    In Ocean Island Basalts (OIB), relationships between helium isotopes and heavy radiogenic isotopes, like 87Sr/86Sr, are often used to constrain the evolution of the mantle. In OIB, 87Sr/86Sr is often measured on whole rock powders, while 3He/4He is measured in olivine hosted melt inclusions. Comparing these values is robust so long as both reservoirs have the same 87Sr/86Sr. However, new evidence suggests significant 87Sr/86Sr disequilibrium can exist between OIB whole rocks and the olivines they host. The data presented show 87Sr/86Sr can vary by ~2000 ppm between the whole rock (0.7089) and olivine hosted melt inclusions (0.7075) in fresh, zero-age Samoan basalts. Additionally, samples with the highest whole rock 87Sr/86Sr also show the greatest disequilibrium between whole rocks and olivines. Importantly, Sr is highly incompatible in the olivine lattice, thus melt inclusions host nearly all Sr in olivines; measuring pooled olivines provides an average 87Sr/86Sr for the melt inclusion population. The origin of whole rock- olivine 87Sr/86Sr disequilibrium is not well understood. The assimilation of seawater derived components could produce this effect, but is inconsistent with Cl/K data collected on submarine glasses. Whole rock 87Sr/86Sr increases with silica content suggesting 87Sr/86Sr disequilibrium is the result of mixing magmas derived from heterogeneous mantle sources. If olivine crystalizes from a low 87Sr/86Sr reservoir, and later mixes with a higher 87Sr/ 86Sr magma, the signature of the initial magma would be captured in the melt inclusions. This whole rock- olivine 87Sr/86Sr disequilibrium has the potential to revolutionize our understanding of the relationships between 3He/4He and 87Sr/86Sr in OIB. These relationships are central to chemical geodynamic models, and establishing a new method for measuring both He and Sr isotopes in olivine hosted melt inclusions will provide new frontiers for future research exploring the noble gas evolution of the

  4. Oxidation state of mercury in HgBa{sub 2}(Ca{sub 0.86}Sr{sub 0.14}){sub 2}Cu{sub 3}O{sub 8+{delta}} studied by x-ray photoelectron spectroscopy

    SciTech Connect

    Gopinath, C.S.; Hur, N.H.; Subramanian, S.

    1995-10-01

    Hg 4{ital f} core levels of HgBa{sub 2}(Ca{sub 0.86}Sr{sub 0.14}){sub 2}Cu{sub 3}O{sub 8+{delta}} (Hg-1223) and HgO were measured by x-ray photoelectron spectroscopy in order to demonstrate the oxidation state of mercury ions in the superconducting oxide. The binding energy of the Hg 4{ital f}{sub 7/2} level is found to be at 99.9 eV in HgO and 101.0 and 103.4 eV in Hg-1223. This result reveals that the oxidation state of Hg is definitely more than +2 and it exists in a mixed-valent state. The creation of charge carriers in Hg-1223 is discussed in terms of a charge transfer between Hg-O{sub {delta}} and Cu-O layers.

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

    SciTech Connect

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

    2005-12-27

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

  6. Strontium isotope constraint on the genesis of crude oils, oil-field brines and Kuroko ore deposits from the Green Tuff region of northeastern Japan

    NASA Astrophysics Data System (ADS)

    Nakano, Takanori; Kajiwara, Yoshimichi; Farrell, Clifton W.

    1989-10-01

    Crude oils from Akita to northern Niigata oil fields in the Green Tuff region of northeastern Japan have distinctly uniform 87Sr/86Sr ratios (0.7080-0.7082), while those from the southern Niigata oil field contain more radiogenic strontium (0.7095-0.7102). The regional variation in the strontium isotopic composition of crude oils is also reflected in their sulfur contents and sulfur isotopic compositions, and may be attributed to the regional heterogeneity of marine organic sediments from which the crude oils were ultimately derived. The 87Sr/86Sr ratios of most oil-field brines (0.7061-0.7084), however, are different from and vary more locally than those of the accompanying crude oils. This finding supports the view that strontium, and by inference some other dissolved solutes in the brines, may have evolved during diagenesis by reaction of a connate and/or a meteoric water with rocks in the Green Tuff region. Barites in the sulfide ore and anhydrites and gypsums in the sulfate (sekko) ore from the Fukazawa and Kosaka Kuroko deposits in the Hokuroku district are divided by the 87Sr/86Sr ratio of 0.7081 (±0.0001), which is identical to that of crude oils from nearby oil fields. This similarity in ratios lends support to the conclusion that the Kuroko base metal deposits and crude oil deposits were ultimately derived from a common organic sediment named PUMOS (Primitive Undifferentiated Metalliferous Organic Sediments).

  7. Carbon isotope ratios of Phanerozoic marine cements: Re-evaluating the global carbon and sulfur systems

    NASA Astrophysics Data System (ADS)

    Carpenter, Scott J.; Lohmann, Kyger C.

    1997-11-01

    Original δ 13C values of abiotically precipitated marine cements from a variety of stratigraphic intervals have been used to document secular variations in the δ 13C values of Phanerozoic oceans. These, together with the ° 34S values of coeval marine sulfates, are used to examine the global cycling of carbon and sulfur. It is generally accepted that secular variation in δ 13C and δ 34S values of marine carbonates and sulfates is controlled by balanced oxidation-reduction reactions and that their long-term, steady-state variation can be predicted from the present-day isotopic fractionation ratio (Δ c/Δ s) the ratio of the riverine flux of sulfur and carbon ( Fs/ Fc). The predicted slope of the linear relation between δ 13C carb and δ 34S sulfate values is approximately -0.10 to -0.14. However, temporal variation observed in marine cement δ 13C values and the 6345 values of coeval marine sulfates produces a highly significant linear relation ( r2 = 0.80; α > 95%) with a slope of -0.24; approximately twice the predicted value. This discordance suggests that either the Phanerozoic average riverine Fs/ Fc was 1.6-3.3 times greater than today's estimates or that an additional source of 34S-depleted sulfur or 13C-enriched carbon, other than continental reservoirs, was active during the Phanerozoic. This new relation between marine δ 13C and δ 34S values suggests that the flux of reduced sulfur, iron, and manganese from seafloor hydrothermal systems affects oceanic O2 levels which, in turn, control the oxidation or burial of organic matter, and thus the δ 13C value of marine DIC. Therefore, the sulfur system (driven by seafloor hydrothermal systems) controls the carbon system rather than organic carbon burial controlling the response of δ 34S values (via formation of sedimentary pyrite). Secular variation of marine 87Sr/86Sr ratios and δ 13C values argues for a coupling of δ 34S and δ 34S values to variation in the relative contribution of seafloor

  8. Exploring the temporal change in provenance encoded in the late Quaternary deposits of the Ganga Plain

    NASA Astrophysics Data System (ADS)

    Agrawal, Shailesh; Sanyal, Prasanta; Balakrishnan, Srinivasan; Dash, Jitendra K.

    2013-07-01

    Temporal analysis of Sr isotopes in soil carbonates and Sr and Nd isotopes in silicate fractions has been carried out in a sedimentary core (Kalpi core; 50 m long) raised from the southern bank of the Yamuna river, Ganga Plain, India. The aim of the study is to constrain sediment provenance through comparison with the modern Himalayan and peninsular river systems' water and bank sediments. Sr isotopic data in soil carbonates (0.71874 to 0.71410) and Srsbnd Nd isotopic data in silicate (0.72865 to 0.74544 and - 13.9 to - 17.2, respectively) vary significantly with depth and are indicative of both Himalayan and peninsular sources for sediments in the southern Ganga Plain. The positive correlation between 87Sr/86Sr ratio and 1/Sr in soil carbonate and the negative correlation between 87Sr/86Sr and ɛNd in silicate confirm mixing of sediments from these sources. Variations of 87Sr/86Sr ratios in soil carbonates show that at ~ 80 and 45 ka the Himalaya acted as the major source of sediments in the southern part of the Ganga Plain. The gradual decrease in 87Sr/86Sr ratios after 80 and 45 ka indicates change in source to peninsular India which is also supported by limited Sr and Nd isotope data in silicates. The change in sediment provenance corresponds well with the available climatic record and is suggestive of strong climatic control in sediment supply with high supply from the Himalaya during the interglacial period and peninsular sediments during glacial period.

  9. Estimating groundwater mixing and origin in an overexploited aquifer in Guanajuato, Mexico, using stable isotopes (strontium-87, carbon-13, deuterium and oxygen-18).

    PubMed

    Horst, Axel; Mahlknecht, Jürgen; Merkel, Broder J

    2007-12-01

    Stable Isotopes (strontium-87, deuterium and oxygen-18, carbon-13) have been used to reveal different sources of groundwater and mixing processes in the aquifer of the Silao-Romita Valley in the state of Guanajuato, Mexico. Calcite dissolution appeared to be the main process of strontium release leading to relatively equal (87)Sr/(86)Sr ratios of 0.7042-0.7062 throughout the study area which could be confirmed by samples of carbonate rocks having similar Sr ratios (0.7041-0.7073). delta(13)C values (-11.91- -6.87 per thousand VPDB) of groundwaters confirmed the solution of carbonates but indicated furthermore influences of soil-CO(2). Deuterium and (18)O contents showed a relatively narrow range of-80.1- -70.0 per thousand VSMOW and -10.2- -8.8 per thousand, VSMOW, respectively but are affected by evaporation and mixing processes. The use of delta(13)C together with (87)Sr/(86)Sr revealed three possible sources: (i) carbonate-controlled waters showing generally higher Sr-concentrations, (ii) fissure waters with low-strontium contents and (iii) infiltrating water which is characterized by low delta(13)C and (87)Sr/(86)Sr ratios. The third component is affected by evaporation processes taking place before and during infiltration which might be increased by extraction and reinfiltration (irrigation return flow).

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

    SciTech Connect

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

    1981-04-10

    We have measured Rb and Sr concentrations and Sr isotopic compositions in 41 whole-rock samples and 12 mineral separates from units of the Samail ophiolite, including peridotite, gabbro, plagiogranite diabase dikes, and gabbro and websterite dikes within the metamorphic peridotite. Ten samples of cummulate gabbro from the Wadir Kadir section and nine samples from the Wadi Khafifah section have mean /sup 87/Sr//sup 86/Sr ratios and standard deviations of 0.70314 +- 0.00030 and 0.70306 +- 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 midocean ridge basalt. The /sup 87/Sr//sup 86/Sr ratios of noncumulate gabbro, plagiogranite, and diabase dikes range from 0.7034 to 0.7047, 0.7038 to 0.7046, and 0.7037 to 0.7061, respectively. These higher /sup 87/Sr//sup 86/Sr ratios are due to alteration of initial magmatic compositions by hydrothermal exchange with seawater. Mineral separates from dikes 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 dikes were derived from partial melting of source regions that had similar long-term histories and chemical compositions.

  11. Strontium and oxygen isotopic evidence for strike/slip movement of accreted terranes in the Idaho Batholith

    NASA Astrophysics Data System (ADS)

    King, Elizabeth M.; Beard, Brian L.; Valley, John W.

    2007-07-01

    The oxygen and strontium isotope compositions of granitic rocks of the Idaho Batholith provide insight into the magma source, assimilation processes, and nature of the suture zone between the Precambrian craton and accreted arc terranes. Granitic rocks of the Idaho Batholith intrude basement rocks of different age: Triassic/Jurassic accreted terranes to the west of the Salmon River suture zone and the Precambrian craton to the east. The age difference in the host rocks is reflected in the abrupt increase in the initial 87Sr/ 86Sr ratios of granitic rocks in the batholith across the previously defined 0.706 line. Initial 87Sr/ 86Sr ratios of granitic rocks along Slate Creek on the western edge of the batholith jump from less than 0.704 to greater than 0.707 along an approximately 700 m transect normal to the Salmon River suture. Initial 87Sr/ 86Sr ratios along the Slate Creek transect do not identify a transition zone between accreted arcs and the craton and suggest a unique tectonic history during or after suturing that is not documented along other transects on the west side of the Idaho Batholith. The lack of transition zone along Slate Creek may be a primary structure due to transcurrent/transpressional movement rather than by contractional thrust faulting during suturing or be the result of post-imbrication modification.

  12. 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.

  13. 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

  14. Strontium isotope geochemistry of groundwaters and streams affected by agriculture, Locust Grove, MD

    USGS Publications Warehouse

    Böhlke, J.K.; Horan, M.

    2000-01-01

    The effects of agriculture on the isotope geochemistry of Sr were investigated in two small watersheds in the Atlantic coastal plain of Maryland. Stratified shallow oxic groundwaters in both watersheds contained a retrievable record of increasing recharge rates of chemicals including NO3/-, Cl, Mg, Ca and Sr that were correlated with increasing fertilizer use between about 1940 and 1990. The component of Sr associated with recent agricultural recharge was relatively radiogenic (87Sr/86Sr = 0.715) and it was overwhelming with respect to Sr acquired naturally by water-rock interactions in the oxidized, non-calcareous portion of the saturated zone. Agricultural groundwaters that penetrated relatively unoxidized calcareous glauconitic sediments at depth acquired an additional component of Sr from dissolution of early tertiary marine CaCO3 (87Sr/86Sr=0.708) while undergoing O2 reduction and denitrification. Ground-water discharge contained mixtures of waters of various ages and redox states. Two streams draining the area are considered to have higher 87Sr/86Sr ratios and NO3/- concentrations than they would in the absence of agriculture; however, the streams have consistently different 87Sr/86Sr ratios and NO3/- concentrations because the average depth to calcareous reducing (denitrifying) sediments in the local groundwater flow system was different in the two watersheds. The results of this study indicate that agriculture can alter significantly the isotope geochemistry of Sr in aquifers and streams and that the effects could vary depending on the types, sources and amounts of fertilizers added, the history of fertilizer use and groundwater residence times. (C) 2000 Elsevier Science Ltd.

  15. Isotopic and chemical constraints on the petrogenesis of Blackburn Hills volcanic field, western Alaska

    SciTech Connect

    Moll-Stalcup, E.J.; Arth, J.G. )

    1991-12-01

    The Blackburn Hills volcanic field is one of several Late Cretaceous and early Tertiary (75-50 Ma) volcanic fields in western Alaska that comprise a vast magmatic province extending from the Arctic Circle to Bristol Bay. It consists of andesite flows, rhyolite domes, a central granodiorite to quartz monzonite pluton, and small intrusive rhyolite porphyries, overlain by basalt and alkali-rhyolites. Most of the field consists of andesite flows which can be divided into two groups on the basis of elemental and isotopic composition: a group having lower ({sup 87}Sr/{sup 86}Sr){sub i}, higher ({sup 143}Nd/{sup 144}Nd){sub i}, and moderate LREE and HREE contents (group 1), and a group having higher ({sup 87}Sr/{sup 86}Sr){sub i}, lower ({sup 143}Nd/{sup 144}Nd){sub i}, and lower HREE contents. Basalts are restricted to the top of the stratigraphic section, comprise the most primitive part of group 1 (({sup 87}Sr/{sup 86}Sr){sub i} = 0.7033; ({sup 143}Nd/{sup 144}Nd){sub i} = 0.5129), and have trace-element ratios that are similar to those of oceanic island basalts (OIBs). Although some workers have suggested that the volcanic field is underlain by old continental crust, none of the data require the presence of Paleozoic or Precambrian continental middle or upper crust under this part of the volcanic field. However, the ultimate source of some of the rocks in the Yukon-Koyukuk province that have high {sup 87}Sr/{sup 86}Sr and low {sup 143}Nd/{sup 144}Nd ratios may be old sub-continental mantle and/or lower crust, which was previously subducted beneath the Yukon-Koyukuk province during Early Cretaceous arc-continent collision.

  16. Petrochemical and isotopic studies of Transhimalayan granites in Ladakh, NW India

    SciTech Connect

    Srimal, N.; Basu, A.R.; Sinha, A.K.

    1985-01-01

    The India-Asia collision zone in the Transhimalayan Indus and Shyok Tectonic Belts (STB) of Ladakh, NW India is characterized by two major granitic batholiths. The northern, Karakoram Granitic batholith and the southern, Ladakh Granitic batholith are separated by thrust-bound belts of ophiolite, flysch and calc-alkaline volcanics of Mesozoic to Tertiary age. The KGC can be divided into three zones: a northern zone of metaluminous to mildly peraluminous granodiorite, diorite and tonalite with normative corundum, a southern zone of peraluminous two-mica and garnet bearing granites with normative corundum 1.8-3.3%, K/Rb=200-310, Rb/Sr > 0.3 and initial /sup 87/Sr/ /sup 86/Sr > 0.7113, and a central zone with variable K/Rb, Rb/Sr and initial /sup 87/Sr//sup 86/Sr ratios showing characteristics of both the northern and the southern zones. Field and characteristics of both the northern and the southern zones. Field and geochemical data indicate that: 1) the northern granites of the KGC represent an older magmatic arc derived largely from igneous sources with a small admixture of evolved crustal components and 2) the southern granites of the KGC are derived by partial melting of mature crustal material. Preliminary work in the LGC indicate varying source contamination reflected in variable initial /sup 87/Sr//sup 86/Sr ratios (.7041-.7072) and in correlated /sup 87/Sr//sup 86/Sr vs. delta /sup 18/O plot. The authors data suggest: 1) multiple accretion of Gondwanic fragments in the Mesozoic and Tertiary along the southern margin of Asia, 2) absence of extensive crustal anatexis in the source region of the Ladakh batholith, and 3) remobilization of old sutures and crustal anatexis as a result of India-Asia collision.

  17. Isotopic and chemical constraints on the petrogenesis of Blackburn Hills volcanic field, western Alaska

    USGS Publications Warehouse

    Moll-Stalcup, E. J.; Arth, Joseph G.

    1991-01-01

    The Blackburn Hills volcanic field is one of several Late Cretaceous and early Tertiary (75-50 Ma) volcanic fields in western Alaska that comprise a vast magmatic province extending from the Arctic Circle to Bristol Bay. It consists of andesite flows, rhyolite domes, a central granodiorite to quartz monzonite pluton, and small intrusive rhyolite porphyries, overlain by basalt and alkali-rhyolites. Most of the field consists of andesite flows which can be divided into two groups on the basis of elemental and isotopic composition: a group having lower ( 87Sr 86Sr)i, higher ( 143Nd 144Nd)i, and moderate LREE and HREE contents (group 1), and a group having higher ( 87Sr 86Sr)i, lower ( 143Sr 144Sr)i, and lower HREE contents. Basalts are restricted to the top of the stratigraphic section, comprise the most primitive part of group 1 [( 87Sr 86Sr)i = 0.7033; ( 143Nd 144Nd)i = 0.5129], and have trace-element ratios that are similar to those of oceanic island basalts (OIBs). In contrast to the basalts, group 1 andesites have higher ( 87Sr 86Sr)i and lower ( 143Nd 144Nd)i, and represent interaction of mantle-derived magmas with the lower crust of Koyukuk terrane. Group 2 andesites have ( 87Sr 86Sr)i and ( 143Nd 144Nd)i that are near bulk-earth values and probably formed by partial melting of the lower crust of Koyukuk terrane. The central pluton and rhyolite porphyries are isotopically uniform ( 87Sr 86Sr)i ??? 0.704, ( 143Nd 144Nd)i ??? 0.51275, and are interpreted to have formed by melting of young mafic to intermediate crustal rocks or by fractionation of group 1 andesites. The rhyolite domes have an isotopic range similar to that of the basalts and andesites [( 87Sr 86Sr)i = 0.70355-0.70499; ( 143Nd 144Nd)i = 0.51263-0.51292], which suggests they formed by fractionation of the and site and basalt magmas. Although some workers have suggested that the volcanic field is underlain by old continental crust, none of the data require the presence of Paleozoic or Precambrian

  18. 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.

  19. Lau Basin basalts (LBB): trace element and Sr sbnd Nd isotopic evidence for heterogeneity in backarc basin mantle

    NASA Astrophysics Data System (ADS)

    Volpe, Alan M.; Douglas Macdougall, J.; Hawkins, James W.

    1988-10-01

    Diverse 87Sr/ 86Sr and 143Nd/ 144Nd isotopic compositions among basalts from the Lau Basin (LBB), an active backarc basin in the southwest Pacific, indicate heterogeneity in the underlying mantle. Isotopic compositions display bimodal distributions which are related to geographic location. Type I LBB ( 87/Sr 86Sr ⩽ 0.70366; 143Nd/ 144Nd ⩾ 0.51297) include tholeiites from the central basin, Peggy Ridge, and Rochambeau Bank, while Type II basaltic and andesitic glasses from the northeastern portion of the basin, near Niua Fo'ou island, have higher 87Sr/ 86Sr ( ⩾ 0.7038) and lower 143Nd/ 144Nd ( ⩽ 0.51288). Both depleted (e.g. N-MORB) and enriched (e.g. E-MORB) trace element abundances occur among Type I and Type II LBB. Covariation between trace element and isotopic ratios among Type I LBB is consistent with mixing between depleted mantle similar to the source for MORB and relatively enriched peridotite similar to the source for E-MORB. Relative to MORB, uniformly high 87Sr/ 86Sr ( +0.0005) among all Type I LBB for given Nd isotopic compositions ( ɛ Nd = +8 to +12) may reflect a lithospheric component, such as ancient recycled altered ocean crust. Type II LBB have Sr sbnd Nd isotopic compositions which are gradational between enriched mantle similar to the source of OIB and a component with distinct Sr isotopic composition such as that observed in Samoan post-erosional basalts. Isotopic and geographic discontinuity between Type I and Type II LBB, and isotopic affinity of Type II and Niua Fo`ou island basalts with those from Samoa suggests that volcanism in the northeastern portion of the basin is tapping deeper mantle beneath the adjoining Pacific plate, as well as Indo-Australian mantle overlying the Pacific lithosphere that is subducted into the Tonga Trench.

  20. Dolomite from reflux of moderate salinity brine, Enewetak Atoll

    SciTech Connect

    Goldstein, R.H.

    1996-12-31

    Dolomite from the Eocene of Enewetak Atoll provides a model for prediction of dolomite reservoirs. Others have noted dolomite below about 1200 meters at the base of permeable slope strata, and that dolomite postdates compaction, formed from fluids with {sup 87}Sr/{sup 86}Sr higher than the host strata, and that dolomite stable isotope values argue for precipitation from cool seawater or warm evaporated seawater. Dolomite contains cloudy cores, rich in primary fluid inclusions. Fluid inclusion ice melting ranges from -2.4 to -4.4{degrees}C (higher salinity than seawater; 44 to 85 ppt). Ratios of clear rim/cloudy core compared to new {sup 87}Sr/{sup 86}Sr and stable isotope data yield no correlation indicative of differences between clear rims and cloudy cores. Dolomite {sup 87}Sr/{sup 86}Sr are 0.70750 to 0.70873, but fluid inclusion {sup 87}Sr/{sup 86}Sr are 0.70957 to 0.71198, indicating inclusions best preserve end-member compositions for the dolomitizing fluid. Thus, dolomite precipitated from a young fluid that, surprisingly, may have interacted with some unknown source of radiogenic Sr. For fluid inclusions, Na/K is similar to seawater indicating components were derived from seawater evaporation and not from dissolution of an evaporate, Na/Sr and Ca/Mg are similar to seawater modified by rock/water interaction, and Cl/SO{sub 4} suggests removal of SO{sub 4} from pore fluids. The only viable explanation for the Enewetak dolomite is that young fluids evaporated to salinities slightly above seawater in Enewetak lagoon. The density contrast allowed for reflux deep into the atoll, discharging through permeable slope strata. This model could predict distributions of dolomite in any platform with slight restriction and appropriate climate.

  1. Dolomite from reflux of moderate salinity brine, Enewetak Atoll

    SciTech Connect

    Goldstein, R.H. )

    1996-01-01

    Dolomite from the Eocene of Enewetak Atoll provides a model for prediction of dolomite reservoirs. Others have noted dolomite below about 1200 meters at the base of permeable slope strata, and that dolomite postdates compaction, formed from fluids with [sup 87]Sr/[sup 86]Sr higher than the host strata, and that dolomite stable isotope values argue for precipitation from cool seawater or warm evaporated seawater. Dolomite contains cloudy cores, rich in primary fluid inclusions. Fluid inclusion ice melting ranges from -2.4 to -4.4[degrees]C (higher salinity than seawater; 44 to 85 ppt). Ratios of clear rim/cloudy core compared to new [sup 87]Sr/[sup 86]Sr and stable isotope data yield no correlation indicative of differences between clear rims and cloudy cores. Dolomite [sup 87]Sr/[sup 86]Sr are 0.70750 to 0.70873, but fluid inclusion [sup 87]Sr/[sup 86]Sr are 0.70957 to 0.71198, indicating inclusions best preserve end-member compositions for the dolomitizing fluid. Thus, dolomite precipitated from a young fluid that, surprisingly, may have interacted with some unknown source of radiogenic Sr. For fluid inclusions, Na/K is similar to seawater indicating components were derived from seawater evaporation and not from dissolution of an evaporate, Na/Sr and Ca/Mg are similar to seawater modified by rock/water interaction, and Cl/SO[sub 4] suggests removal of SO[sub 4] from pore fluids. The only viable explanation for the Enewetak dolomite is that young fluids evaporated to salinities slightly above seawater in Enewetak lagoon. The density contrast allowed for reflux deep into the atoll, discharging through permeable slope strata. This model could predict distributions of dolomite in any platform with slight restriction and appropriate climate.

  2. Strontium-isotope stratigraphy of Enewetak Atoll

    USGS Publications Warehouse

    Ludwig, K. R.; Halley, Robert B.; Simmons, Kathleen R.; Peterman, Zell E.

    1988-01-01

    87Sr/86Sr ratios determined for samples from a 350 m core of Neogene lagoonal, shallow-water limestones from Enewetak Atoll display a remarkably informative trend. Like the recently published data for Deep Sea Drilling Project (DSDP) carbonates, 87Sr/86Sr at Enewetak increases monotonically but not smoothly from the early Miocene to the Pleistocene. The data show intervals of little or no change in 87Sr/86Sr, punctuated by sharp transitions to lower values toward greater core depths. The sharp transitions correlate with observed solution disconformities caused by periods of subaerial erosion, whereas the intervals of little or no change in 87Sr/86Sr correspond to intervals of rapid accumulation of shallow-water carbonate sediments. When converted to numerical ages using the published DSDP 590B trend, the best-resolved time breaks are at 282 m (12.3 to 18.2 Ma missing) and 121.6 m (3.0 to 5.3 Ma missing) below the lagoon floor. At Enewetak, Sr isotopes offer a stratigraphic resolution for these shallow-marine Neogene carbonates comparable to that of nannofossil zonation in deep-sea carbonates (0.3-3 m.y.). In addition, the correlation of times of Sr-isotope breaks at Enewetak with times of rapid Sr-isotope change in the DSDP 590B samples confirms the importance off sea-level changes in the evolution of global-marine Sr isotopes and shows that the Sr-isotope response to sea-level falls is rapid.

  3. Geochemically distinct sources for interstratified lavas from the Nejapa cinder cone alignment, Nicaragua

    SciTech Connect

    Feigenson, M.D.; Carr, J.J.; Walker, J.A.

    1985-01-01

    The Nejapa cinder cone alignment, near Managua, Nicaragua, produces mafic subalkaline basalts that are similar to mid-ocean ridge basalts (MORB). The Nejapa basalts can be divided into high- and low-titanium suites that are interstratified. Although major element compositions are similar to MORB, concentrations of Ba and Sr in the Nejapa basalts are higher, ranging from 2 x MORB in the high-titanium suite to 10 X MORB for the low-titanium lavas. Recently determined Nd and Sr isotopic and rare earth element (REE) concentrations for Nejapa basalts show that the high and low titanium suites have distinct sources and cannot be related by simple crystallization trends. For example, although the high-Ti lavas are light REE depleted and have overall MORB-like REE concentrations, they are systematically lower in /sup 143/Nd//sup 144/Nd and higher in /sup 87/Sr//sup 86/Sr. Low-Ti lavas, on the other hand, are LREE-enriched but have Nd isotopes identical to MORB (/sup 87/Sr//sup 86/Sr is distinctly higher). The contradictory geochemical characteristics displayed by the Nejapa lavas can be explained in a general sense by a mixing model that involves upper mantle peridotite and a fluid derived from hydrothermally-altered subducted oceanic crust. This fluid may enrich overlying mantle in Ba, Sr, and /sup 87/Sr//sup 86/Sr, and may supply enough water to stabilize an accessory phase such as rutile at high pressure. Melts generated from this source will be low in Ti, but high in Ba, Sr, /sup 87/Sr//sup 86/Sr and /sup 143/Nd//sup 144/Nd. Subjacent peridotite melting with less of the hydrous flux will generate lavas with higher Ti, lower Sr and Ba, and isotopic ratios of the peridotite.

  4. Geochemistry of some deep gold mine waters from the western portion of the Witwatersrand Basin, South Africa

    NASA Astrophysics Data System (ADS)

    Duane, M. J.; Pigozzi, G.; Harris, C.

    1997-02-01

    A suite of 12 mine water samples within the Witwatersrand Basin (South Africa) were analysed for trace element concentrations, strontium isotopic composition and stable isotopes (O and H). Chemical profiles for four Au mines (Western Deep Levels, Vaal Reefs, Freddies and President Steyn) are used to infer origin, chemical and isotopic evolution of the brines and for comparison with basement brines from other Precambrian areas. Systematic relationships are observed between {87Sr}/{86Sr} and {1}/{Sr} : two major mixing trends are required to explain the range of very radiogenic end-members. Possible end-members for the two components could be (1) {87Sr}/{86Sr} = 0.7251 , Sr concentration = 0.12 mg l -1 from a Vaal Reefs compartment and {87Sr}/{86Sr} = 0.7694 , Sr = 39.3 mg l -1 from a Freddies compartment. (2) {87Sr}/{86Sr} = 0.7251 , Sr = 0.12 mg l -1 (as above) with a {87Sr}/{86Sr} = 0.7404 , Sr = 745 mg l -1 from Western Deep Levels. Strontium isotope ratios range above those expected for present-day seawater and are even higher than some locally-derived low Rb minerals from the Precambrian basement. The brines acquired radiogenic 87Sr through interaction with granitic basement (Kaapvaal Craton), shales of the Central Rand Group (in particular Ventersdorp Contact Reef), siliclastics within the West Rand Group and particularly with dolomites from the overlying Transvaal Supergroup. In order to obtain their multielement and radiogenic isotope signatures the meteoric waters descended through fractured rocks between the main dykes and faults (example: Oberholzer and Bank Dyke at Western Deep Levels). They slowly interacted with Au bearing conglomerates and quartzites of the West Rand Group. The inverse relationship between Sr isotope composition and precious/heavy metal concentration suggests fluid/rock interaction within the shales and volcanics of the Ventersdsorp Contact Reef (high in Au and total organic carbon [TOC], less radiogenic strontium composition by

  5. Strontium 87/strontium 86 as a tracer of mineral weathering reactions and calcium sources in an alpine/subalpine watershed, Loch Vale, Colorado

    USGS Publications Warehouse

    Clow, D.W.; Mast, M.A.; Bullen, T.D.; Turk, J.T.

    1997-01-01

    Sr isotopic ratios of atmospheric deposition, surface and subsurface water, and geologic materials were measured in an alpine/subalpine watershed to characterize weathering reactions and identify sources of dissolved Ca in stream water. Previous studies have noted an excess of Ca in stream water above that expected from stoichiometric weathering of the dominant bedrock minerals. Mixing calculations based on 87Sr/86Sr indicate that on an annual basis, 26 ?? 7% of Ca export in streams is atmospherically derived, 23 ?? 1% is from weathering of plagioclase, and the remainder is from weathering of calcite present in trace amounts in the bedrock. A potential source of error when applying Sr isotopes in catchment studies is determination of the 87Sr/86Sr of Sr released by mineral weathering, which is complicated by the wide range of mineral isotopic compositions, particularly in older rocks, and the variable rates at which the minerals weather. In this study, base-flow stream chemistry was used to represent the 87Sr/86Sr of Sr derived from mineral weathering because it effectively integrates the potentially variable isotopic composition of Sr released by weathering in the alpine environment.

  6. Characterisation and origin of New Zealand nephrite jade using its strontium isotopic signature

    NASA Astrophysics Data System (ADS)

    Adams, C. J.; Beck, R. J.; Campbell, H. J.

    2007-09-01

    Nephrite jade occurs in three terranes (Dun Mountain-Maitai, Caples and Torlesse) in New Zealand, where it is associated with ultramafic and ophiolitic rocks in narrow metasomatic reaction zones at the margins of serpentinite (having harzburgite/gabbro/dolerite precursors) with silicic metasediments and metavolcanics. True nephrite fabrics are developed only locally where marginal shearing is intense, and late in the metamorphic history. 87Sr/ 86Sr values of these nephrites do not display the primitive values of their gabbro/dolerite precursor component i.e. 0.7030-0.7035, as expected if formed during serpentinisation. Rather, the nephrites have more evolved 87Sr/ 86Sr values inherited from the metasediment component at a later stage, and which fall within particular terrane groups: Dun Mountain-Maitai 0.7045-0.7060, Caples 0.7058-0.7075 and Torlesse 0.7085-0.7110. Rb-Sr ages and initial 87Sr/ 86Sr ratios of the metasediment component from in situ nephrite localities, when compared with their counterparts throughout the host terrane, show that nephrite Sr isotopic compositions are characteristic of the host terrane.

  7. Strontium isotope geochronology of selected intervals within the Florida Neogene

    SciTech Connect

    Jones, D.S.; Mueller, P.A.; Hodell, D.A.; Stanley, L.A. . Dept. of Geology)

    1993-03-01

    The Neogene stratigraphic record of Florida reveals many richly fossiliferous (both invertebrate and vertebrate), shallow-marine deposits whose ages are poorly constrained, despite over a century of paleontological investigation. Chronostratigraphic analyses are frequently hampered by a general absence of age-diagnostic fossils (micro- or nannofossils in particular), laterally discontinuous sedimentary units, and an overall lack of natural exposure. Consequently, temporal correlations among many of Florida's Neogene units as well as with the global geomagnetic polarity timescale (GPTS) remain tenuous. Strontium isotope ([sup 87]Sr/[sup 86]Sr) geochronology offers considerable potential as an independent method for correlating these deposits with one another as well as with the GPTS. Portions of the Miocene and Pliocene as well as most of the Pleistocene were characterized by rapid increases in the global [sup 87]Sr/[sup 86]Sr of seawater. Marine carbonates formed within these intervals are therefore particularly amenable to investigation by Sr isotope techniques. Ratios ([sup 87]Sr/[sup 86]Sr) from mollusk shells collected throughout Florida within stratigraphic context ranged from 0.70785 which roughly correspond to the interval 30 Ma (late Oligocene) to 1 Ma (late Pleistocene). The data suggest that many accepted correlations based on lithologic and/or faunal similarities within Florida's Miocene and Plio-Pleistocene strata are improbable. While additional sampling is in order, improved correlation between vertebrate and invertebrate biochronologies has already resulted from the stratigraphic based upon this approach.

  8. Factors controlling Li concentration and isotopic composition in formation waters and host rocks of Marcellus Shale, Appalachian Basin

    USGS Publications Warehouse

    Phan, Thai T.; Capo, Rosemary C; Stewart, Brian W.; Macpherson, Gwen; Rowan, Elisabeth L.; Hammack, Richard W.

    2015-01-01

    In Greene Co., southwest Pennsylvania, the Upper Devonian sandstone formation waters have δ7Li values of + 14.6 ± 1.2 (2SD, n = 25), and are distinct from Marcellus Shale formation waters which have δ7Li of + 10.0 ± 0.8 (2SD, n = 12). These two formation waters also maintain distinctive 87Sr/86Sr ratios suggesting hydrologic separation between these units. Applying temperature-dependent illitilization model to Marcellus Shale, we found that Li concentration in clay minerals increased with Li concentration in pore fluid during diagenetic illite-smectite transition. Samples from north central PA show a much smaller range in both δ7Li and 87Sr/86Sr than in southwest Pennsylvania. Spatial variations in Li and δ7Li values show that Marcellus formation waters are not homogeneous across the Appalachian Basin. Marcellus formation waters in the northeastern Pennsylvania portion of the basin show a much smaller range in both δ7Li and 87Sr/86Sr, suggesting long term, cross-formational fluid migration in this region. Assessing the impact of potential mixing of fresh water with deep formation water requires establishment of a geochemical and isotopic baseline in the shallow, fresh water aquifers, and site specific characterization of formation water, followed by long-term monitoring, particularly in regions of future shale gas development.

  9. REE Behavior During Anhydrite and Gypsum Formations of the Kuroko Type Massive Sulfide-Sulfate Deposits

    NASA Astrophysics Data System (ADS)

    Ogawa, Yasumasa; Shikazono, Naotatsu

    2006-05-01

    The Sr and rare earth elements (REEs) concentrations and Sr isotopic composition (87Sr/86Sr) of anhydrite and gypsum have been determined for samples from the Matsumine, Shakanai and Hanaoka Kuroko-type massive sulfide-sulfate deposits in the Hokuroku District in Akita Pref. in northern Japan. The anhydrite samples exhibit two styles of chondrite-normalized REE patterns; one with a decrease from light to heavy REEs (Type I), and another with a light REE-depleted pattern with peak in Sm (Type II). The Sr content of Type I anhydrite is higher than that of Type II. The 87Sr/86Sr ratios of all anhydrite samples are intermediate between that of middle Miocene seawater and that of country rocks. 87Sr/86Sr of Type I anhydrite is closer to Miocene seawater, and that of Type II is closer to the country rocks. Based on the Sr data obtained by this study and previous reports on geochemical data on the Kuroko mineralization, geochemical environment of anhydrite formation was investigated. However, from that investigation, it is inferred that REE fractionation would not occur during the primary anhydrite precipitation. Gypsum, which partially replaces anhydrite in the Kuroko deposits, also exhibits two distinct chondrite-normalized REE patterns. Because LREEs are likely to be more easily mobilized during the secondary process such as dissolution and re-crystallization, it is hypothesized that LREE release from Type I anhydrite, resulting in the formation of secondary Type II anhydrite with LREE depleted profiles.

  10. Trace element and strontium isotope characteristics of volcanic rocks from Isla Tortuga: a young seamount in the Gulf of California

    USGS Publications Warehouse

    Batiza, Rodey; Futa, K.; Hedge, C.E.

    1979-01-01

    Isla Tortuga is a small isolated central volcano which is located near an actively spreading trough in the Gulf of California. The basalt lavas from Tortuga which have the highest Mg/Fe and Ni contents have trace element abundances and ratios and 87Sr/86Sr which are similar to those of mid-ocean ridge tholeiite. The major element, rare earth element and Sr abundances of fractionated tholeiite (low Mg/Fe) and tholeiitic andesite of Tortuga are consistent with an origin by closed-system fractional crystallization. This hypothesis is not supported by K, Na, Rb and Ba abundances in the lavas nor by their variable 87Sr/86Sr (0.7024-0.7035). It is proposed that the apparent decoupling of light rare earth elements, other incompatible trace elements and 87Sr/86Sr is due to contamination of some Tortuga magmas while they are fractionated in a high-level crustal magma chamber. The mantle source of least-contaminated, high Mg/Fe basalt lavas of Tortuga is similar, although not identical to the source of normal mid-ocean ridge tholeiite; significant differences exist. The reasons for these differences are not yet known. ?? 1979.

  11. Precision measurement of the 5 {sup 2}S{sub 1/2}- 4 {sup 2}D{sub 5/2} quadrupole transition isotope shift between {sup 88}Sr{sup +} and {sup 86}Sr{sup +}

    SciTech Connect

    Lybarger, Warren E. Jr.; Berengut, Julian C.; Chiaverini, John

    2011-05-15

    We present a high-precision measurement of the isotope shift of the narrow quadrupole-allowed 5 {sup 2}S{sub 1/2}- 4 {sup 2}D{sub 5/2} transition in {sup 86}Sr{sup +} relative to the most abundant isotope {sup 88}Sr{sup +}. This was accomplished using high-resolution laser spectroscopy of individual trapped ions, and the measured shift is {Delta}{nu}{sub meas}{sup 88,86}=570.281(4) MHz. We also tested a recently developed and successful method for ab initio calculation of isotope shifts in alkali-metal-like atomic systems against this measurement, and our initial result of {Delta}{nu}{sub calc}{sup 88,86}=457(28) MHz is also presented. While the measurement and the calculation are in broad agreement, there is a clear discrepancy between them, and we believe that the specific mass shift was underestimated in our calculation. Our measurement provides a stringent test for further refinements of theoretical isotope shift calculation methods for atomic systems with a single valence electron.

  12. Tracking natural and anthropogenic origins of dissolved arsenic during surface and groundwater interaction in a post-closure mining context: Isotopic constraints.

    PubMed

    Khaska, Mahmoud; Le Gal La Salle, Corinne; Verdoux, Patrick; Boutin, René

    2015-01-01

    Arsenic contamination of stream waters and groundwater is a real issue in Au-As mine environments. At the Salsigne Au-As mine, southern France, arsenic contamination persists after closure and remediation of the site. In this study, natural and anthropogenic arsenic inputs in surface water and groundwater are identified based on (87)Sr/(86)Sr, and δ(18)O and δ(2)H isotopic composition of water. In the wet season, downstream of the remediated zone, the arsenic contents in stream water and alluvial aquifer groundwater are high, with values in the order of 36 μg/L and 40 μg/L respectively, while upstream natural background average concentrations are around 4 μg/L. Locally down-gradient of the reclaimed area, arsenic concentrations in stream water showed 2 peaks, one during an important rainy event (101 mm) in the wet season in May, and a longer one over the dry period, reaching 120 and 110 μg/L respectively. The temporal variations in arsenic content in stream water can be explained i) during the dry season, by release of arsenic stored in the alluvial sediments through increased contribution from base flow and decreased stream flow and ii) during major rainy events, by mobilization of arsenic associated with important surface runoff. The (87)Sr/(86)Sr ratios associated with increasing arsenic content in stream waters downstream of the reclaimed area are significantly lower than that of the natural Sr inherited from Variscan formations. These low (87)Sr/(86)Sr ratios are likely to be associated with the decontaminating water treatment processes, used in the past and still at present, where CaO, produced from marine limestone and therefore showing a low (87)Sr/(86)Sr ratios, is used to precipitate Ca3(AsO4)2. The low Sr isotope signatures will then impact on the Sr isotope ratio of (1) the Ca-arsenate stored in tailing dams, (2) effluent currently produced by water treatment process and (3) groundwater draining from the overall site. Furthermore, Δ(2)H shows

  13. Tracking natural and anthropogenic origins of dissolved arsenic during surface and groundwater interaction in a post-closure mining context: Isotopic constraints

    NASA Astrophysics Data System (ADS)

    Khaska, Mahmoud; Le Gal La Salle, Corinne; Verdoux, Patrick; Boutin, René

    2015-06-01

    Arsenic contamination of stream waters and groundwater is a real issue in Au-As mine environments. At the Salsigne Au-As mine, southern France, arsenic contamination persists after closure and remediation of the site. In this study, natural and anthropogenic arsenic inputs in surface water and groundwater are identified based on 87Sr/86Sr, and δ18O and δ2H isotopic composition of water. In the wet season, downstream of the remediated zone, the arsenic contents in stream water and alluvial aquifer groundwater are high, with values in the order of 36 μg/L and 40 μg/L respectively, while upstream natural background average concentrations are around 4 μg/L. Locally down-gradient of the reclaimed area, arsenic concentrations in stream water showed 2 peaks, one during an important rainy event (101 mm) in the wet season in May, and a longer one over the dry period, reaching 120 and 110 μg/L respectively. The temporal variations in arsenic content in stream water can be explained i) during the dry season, by release of arsenic stored in the alluvial sediments through increased contribution from base flow and decreased stream flow and ii) during major rainy events, by mobilization of arsenic associated with important surface runoff. The 87Sr/86Sr ratios associated with increasing arsenic content in stream waters downstream of the reclaimed area are significantly lower than that of the natural Sr inherited from Variscan formations. These low 87Sr/86Sr ratios are likely to be associated with the decontaminating water treatment processes, used in the past and still at present, where CaO, produced from marine limestone and therefore showing a low 87Sr/86Sr ratios, is used to precipitate Ca3(AsO4)2. The low Sr isotope signatures will then impact on the Sr isotope ratio of (1) the Ca-arsenate stored in tailing dams, (2) effluent currently produced by water treatment process and (3) groundwater draining from the overall site. Furthermore, Δ2H shows that the low 87Sr/86Sr

  14. Tracking natural and anthropogenic origins of dissolved arsenic during surface and groundwater interaction in a post-closure mining context: Isotopic constraints.

    PubMed

    Khaska, Mahmoud; Le Gal La Salle, Corinne; Verdoux, Patrick; Boutin, René

    2015-01-01

    Arsenic contamination of stream waters and groundwater is a real issue in Au-As mine environments. At the Salsigne Au-As mine, southern France, arsenic contamination persists after closure and remediation of the site. In this study, natural and anthropogenic arsenic inputs in surface water and groundwater are identified based on (87)Sr/(86)Sr, and δ(18)O and δ(2)H isotopic composition of water. In the wet season, downstream of the remediated zone, the arsenic contents in stream water and alluvial aquifer groundwater are high, with values in the order of 36 μg/L and 40 μg/L respectively, while upstream natural background average concentrations are around 4 μg/L. Locally down-gradient of the reclaimed area, arsenic concentrations in stream water showed 2 peaks, one during an important rainy event (101 mm) in the wet season in May, and a longer one over the dry period, reaching 120 and 110 μg/L respectively. The temporal variations in arsenic content in stream water can be explained i) during the dry season, by release of arsenic stored in the alluvial sediments through increased contribution from base flow and decreased stream flow and ii) during major rainy events, by mobilization of arsenic associated with important surface runoff. The (87)Sr/(86)Sr ratios associated with increasing arsenic content in stream waters downstream of the reclaimed area are significantly lower than that of the natural Sr inherited from Variscan formations. These low (87)Sr/(86)Sr ratios are likely to be associated with the decontaminating water treatment processes, used in the past and still at present, where CaO, produced from marine limestone and therefore showing a low (87)Sr/(86)Sr ratios, is used to precipitate Ca3(AsO4)2. The low Sr isotope signatures will then impact on the Sr isotope ratio of (1) the Ca-arsenate stored in tailing dams, (2) effluent currently produced by water treatment process and (3) groundwater draining from the overall site. Furthermore, Δ(2)H shows

  15. Determination of Sr isotopes in calcium phosphates using laser ablation inductively coupled plasma mass spectrometry and their application to archaeological tooth enamel

    NASA Astrophysics Data System (ADS)

    Horstwood, M. S. A.; Evans, J. A.; Montgomery, J.

    2008-12-01

    The determination of accurate Sr isotope ratios in calcium phosphate matrices by laser ablation multi-collector ICP-MS is demonstrated as possible even with low Sr concentration archaeological material. Multiple on-line interference correction routines for doubly-charged REE, Ca dimers and Rb with additional calibration against TIMS-characterised materials are required to achieve this. The calibration strategy proposed uses both inorganic and biogenic apatite matrices to monitor and correct for a 40Ca- 31P- 16O polyatomic present at levels of 0.3-1% of the non-oxide peak, which interferes on 87Sr causing inaccuracies of 0.03-0.4% in the 87Sr/ 86Sr isotope ratio. The possibility also exists for synthetic materials to be used in this calibration. After correction for interferences total combined uncertainties of 0.04-0.15% (2SD) are achieved for analyses of 13-24 μg of archaeological tooth enamel with Sr concentrations of ca. 100-500 ppm using MC-ICP-MS. In particular, for samples containing >300 ppm Sr, total uncertainties of ˜0.05% are possible utilising 7-12 ng Sr. Data quality is monitored by determination of 84Sr/ 86Sr ratios. When applied to an archaeological cattle tooth this approach shows Sr-isotope variations along the length of the tooth in agreement with independent TIMS data. The 40Ca- 31P- 16O polyatomic interference is the root cause of the bias at mass 87 during laser ablation ICP-MS analysis of inorganic and biogenic calcium phosphate (apatite) matrices. This results in inaccurate 87Sr/ 86Sr ratios even after correction of Ca dimers and doubly charged rare earth elements. This interference is essentially constant at specific ablation conditions and therefore the effect on 87Sr/ 86Sr data varies in proportion to changes in the Sr concentration of the ablated material. Complete elimination of this interference is unlikely through normal analytical mechanisms and therefore represents a limitation on the achievable accuracy of LA-(MC-)ICP-MS 87Sr/ 86Sr

  16. 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

  17. Final report of the key comparison CCQM-K98: Pb isotope amount ratios in bronze

    NASA Astrophysics Data System (ADS)

    Vogl, Jochen; Yim, Yong-Hyeon; Lee, Kyoung-Seok; Goenaga-Infante, Heidi; Malinowskiy, Dmitriy; Ren, Tongxiang; Wang, Jun; Vocke, Robert D., Jr.; Murphy, Karen; Nonose, Naoko; Rienitz, Olaf; Noordmann, Janine; Näykki, Teemu; Sara-Aho, Timo; Ari, Betül; Cankur, Oktay

    2014-01-01

    ) were selected such that they correspond with those commonly reported in Pb isotopic studies and fully describe the isotopic composition of Pb in the sample. Additionally, the isotope amount ratio n(208Pb)/n(206Pb) was added, as this isotope ratio is typically measured when performing Pb quantitation by IDMS involving a 206Pb spike. Each participant was free to use any method they deemed suitable for measuring the individual isotope ratios. However, the majority of the results were obtained by using muIti-collector ICPMS or TIMS. The key requirements for all analytical procedures were a traceability statement for all results and the establishment of an uncertainty budget meeting a target uncertainty for all ratios of 0.2 %, relative (k=1). Additionally, the use of a Pb-matrix separation procedure was encouraged. The obtained overall result was excellent, demonstrating that the individual results reported by the NMIs/DIs were comparable and compatible for the determination of Pb isotope ratios. MC-ICPMS and MC-TIMS data were consistent with each other and agree to within 0.05 %. The corresponding uncertainties can be considered as realistic uncertainties and mainly range from 0.02 % to 0.08 % (k=1). As stated above isotope ratios are being increasingly used in different fields. Despite the availability and ease of use of new mass spectrometers, the metrology of unbiased isotope ratio measurements remains very challenging. Therefore, further comparisons are urgently needed, and should be designed to also engage scientists outside the NMI/DI community. Possible follow-up studies should focus on isotope ratio and delta measurements important for environmental and technical applications (e.g. B), food traceability and forensics (e.g. H, C, N, O, S and 87Sr/86Sr) or climate change issues (e.g. Li, B, Mg, Ca, Si). Main text. To reach the main text of this paper, click on Final Report. The final report has been peer-reviewed and approved for publication by the CCQM.

  18. Nd, Sr, Pb, Ar, and O isotopic systematics of Sturgeon Lake kimberlite, Saskatchewan, Canada: constraints on emplacement age, alteration, and source composition

    NASA Astrophysics Data System (ADS)

    Hegner, E.; Roddick, J. C.; Fortier, S. M.; Hulbert, L.

    1995-06-01

    Rb-Sr isotopic dating of phlogopite megacryst samples separated from Sturgeon Lake kimberlite, Saskatchewan, yields a crystallization age of 98±1 Ma (2 σ, MSWD=1.2; 87Sr/86Sr( t)=0.7059). The 40Ar/39Ar analyses of a phlogopite megacryst sample indicate the presence of large amounts of excess 40Ar and yield an excessively old age of ˜410 Ma. Assessment of the Ar data using isotope correlation plots indicates clustering of the data points about a mixing line between the radiogenic 40Ar component at 98 Ma and a trapped component with uniform 36Ar/40Ar and Cl/40Ar. Values of δ 18O as high as +20‰ (VSMOW) for calcite from the groundmass and a whole-rock sample indicate pervasive low-temperature alteration. The δ 13C of matrix carbonate is -11.3‰ (PDB), slightly lighter than typical values from the literature. The δ 18O values of about +5‰ (VSMOW) for brown phlogopite megacrysts may be primary, green phlogopites are interpreted to be an alteration product of the brown variety and are 2‰ heavier. Initial Nd-Sr-Pb isotopic ratios for a whole-rock sample ( ɛ Nd=+0.8; 87Sr/86Sr=0.7063, 206Pb/204Pb=18.67, 207Pb/204Pb=15.54, 208Pb/204Pb=38.97) suggest an affinity with group I kimberlites. Initial ɛ Nd values of +1.7 and +0.5 (87Sr/86Sr( t)=0.7053 and 0.7050) for eclogitic and lherzolitic garnet megacryst samples, and values of 0.0 for two phlogopite megacryst samples reflect an origin from an isotopically evolving melt due to assimilation of heterogeneous mantle. Lilac high-Cr lherzolitic garnet megacrysts give an unusually high ɛ Nd(98. Ma) of +28.6 (87Sr/86Sr=0.7046) indicating a xenocrystic origin probably from the lithospheric mantle. The very radiogenic 87Sr/86Sr and 206Pb/204Pb ratios of the kimberlite are consistent with melting of EM II (enriched) mantle components.

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

    NASA Astrophysics Data System (ADS)

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

    2015-01-01

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

  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. Magma genesis in the lesser Antilles island arc

    NASA Astrophysics Data System (ADS)

    Hawkesworth, C. J.; Powell, M.

    1980-12-01

    143Nd/ 144Nd, 87Sr/ 86Sr and REE results are reported on volcanic rocks from the islands of Dominica and St. Kitts in the Lesser Antilles. Particular attention is given to the lavas and xenoliths of the Foundland (basalt-andesite) and the Plat Pays (andesite-dacite) volcanic centres on Dominica. Combined major and trace element [ 2] and isotope results suggest that the bulk of the andesites and dacites on Dominica, and by analogy in the rest of the arc, are produced by fractional crystallisation of basaltic magma. The differences in the erupted products of the two volcanoes do not appear to be related to any significant differences in the source rocks of the magmas. Along the arc 87Sr/ 86Sr ratios range from 0.7037 on St. Kitts, to 0.7041-0.7047 on Dominica, and 0.7039-0.7058 on Grenada [ 5], and these are accompanied by a parallel increase in K, Sr, Ba and the light REE's. Moreover, compared with LIL-element-enriched and -depleted rocks from MOR and intraplate environments, the basic rocks from the Lesser Antilles are preferentially enriched in alkaline elements (K, Ba, Rb, Sr) relative to less mobile elements such as the rare earths. 143Nd/ 144Nd varies from 0.51308 on St. Kitts, to 0.51286 on Dominica, and 0.51264-0.51308 on Grenada [ 5], and all these samples have relatively high 87Sr/ 86Sr ratios compared with the main trend of Nd and Sr isotopes for most mantle-derived volcanic rocks. Alkaline elements and 87Sr appear to have been introduced from the subducted ocean crust, but the results on other, less mobile elements are more ambiguous — island arc tholeiites (as on St. Kitts) do not appear to contain significant amounts of REE's, Zr, Y, etc., from the subducted oceanic crust, but such a contribution may be present in more LIL-element-enriched calc-alkaline rock types.

  2. Constraints On Fluid Evolution During Mid-Ocean Ridge Hydrothermal Circulation From Anhydrite Sampled by ODP Hole 1256D

    NASA Astrophysics Data System (ADS)

    Smith-Duque, C.; Teagle, D. A.; Alt, J. C.; Cooper, M. J.

    2008-12-01

    Anhydrite is potentially a useful mineral for recording the evolution of seawater-derived fluids during mid- ocean ridge hydrothermal circulation because it exhibits retrograde solubility, and hence may precipitate due to the heating of seawater or the sub-surface mixing of seawater with black smoker-like fluids. Here we provide new insights into the chemical and thermal evolution of seawater during hydrothermal circulation through analyses of anhydrite recovered from ODP Hole 1256D, the first complete penetration of intact upper oceanic crust down to gabbros. Previously, crustal anhydrite has been recovered only from Hole 504B. Measurements of 87Sr/86Sr, major element ratios, Rare Earth Elements and δ18O in anhydrite constrain the changing composition of fluids as they chemically interact with basalt. Anhydrite fills veins and pore-space in the lower lava sequences from ~530 to ~1000 meters sub- basement (msb), but is concentrated in the lava-dike transition (754 to 811 msb) and uppermost sheeted dikes. Although present in greater quantities than in Hole 504B, the amount of anhydrite recovered from the Site 1256 crust is low compared to that predicted by models of hydrothermal circulation (e.g., Sleep, 1991). Two distinct populations of anhydrite are indicated by measurements of 87Sr/86Sr suggesting different fluid evolution paths within Site 1256. One group of anhydrites have 87Sr/86Sr of 0.7070 to 0.7085, close to that of 15 Ma seawater (0.70878), suggesting that some fluids penetrate through the lavas and into the sheeted dikes with only minimal Sr-exchange with the host basalts. A second group, with low 87Sr/86Sr between 0.7048 and 0.7052, indicates precipitation from a fluid that has undergone far greater interaction with basalt. This range is close to that estimated from Sr-isotopic analyses of epidote for the Hole 1256D hydrothermal fluids (87Sr/86Sr ~0.705). Sr/Ca and 87Sr/86Sr indicate a similar relationship to that seen at ODP Hole 504B suggesting that

  3. Unravelling the complex interaction between mantle and crustal magmas encoded in the lavas of San Vincenzo (Tuscany, Italy). Part II: Geochemical overview and modelling

    NASA Astrophysics Data System (ADS)

    Ridolfi, Filippo; Renzulli, Alberto; Perugini, Diego; Cesare, Bernardo; Braga, Roberto; Del Moro, Stefano

    2016-02-01

    This work reports a geochemical overview and modelling of the lavas erupted ~ 4.4 Ma ago at San Vincenzo (Tuscan Magmatic Province, TMP). Although these lavas cover a relatively small area (~ 10 km2), they show very large geochemical variations caused by the interaction of mantle-derived and crustal-anatectic magmas. The lavas consist of peraluminous rhyolites (87Sr/86Sr(i) up to 0.726) hosting primarily variably sized magmatic enclaves with shoshonite/latite compositions (87Sr/86Sr(i) down to 0.708). New whole-rock data for a large shoshonite enclave show high concentrations of LREE, LILE, and tetravalent HFSE, coupled with pentavalent HFSE depletions and enrichments in compatible elements such as Cr and Co. The chondrite-normalised REE pattern is strongly fractionated and characterised by a negative Eu anomaly (Eu/Eu* = 0.79). Hybridisation and AFC models suggest that the shoshonite enclave is the result of 12% rhyolite contamination of a mantle-derived magma akin to the potassic trachybasalt/shoshonite lavas of Capraia Island (~ 4.6 Ma; TMP), following an 18.5% assimilation of Late Triassic metasediments (13% evaporite and 5.5% carbonate) and 56% fractionation of clinopyroxene (39%), plagioclase (10%), and biotite (7%). Each rhyolite sample is characterised by mineral-scale isotopic disequilibria (e.g., 87Sr/86Sr(i) = 0.711-0.726), glass inclusions with large K2O/Na2O variations (1.1-3.4) and a poli-thermobarometric history of crustal melt production at eutectic conditions. A multi-parametric approach accounting for K2O/Na2O (1.3-2.2), 87Sr/86Sr(i) (0.713-0.725), Sr (104-311 ppm) and Rb (294-403 ppm) whole-rock variations, allowed us to divide the anatectic (A) rhyolites into five groups (A1, A2.1, A2.2, A2.3, A3). Group A1 shows the highest 87Sr/86Sr(i) ratios and the lowest values of Sr, K2O/Na2O and Rb. It is related to A2.1 and A3 rhyolites by positive K2O/Na2O-Rb and K2O/Na2O-FeO correlations. These three rhyolite groups crop out in the south of San

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

    NASA Astrophysics Data System (ADS)

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

    2015-10-01

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

  5. Sr isotopic evidence for fluid mixing in ore-stage dolomites, Pine Point, Northwest Territories, Canada

    NASA Astrophysics Data System (ADS)

    Gleeson, S. A.; Gromek, P.; Simonetti, A.

    2009-05-01

    The carbonate hosted Pb-Zn deposits of the Pine Point district (Northwest Territories) are located close to the eastern edge of the present day Western Canadian Sedimentary Basin. The deposits have been classified as Mississippi Valley Type deposits and are thought to have formed as the result of basin-wide fluid flow in the Presqu'ile barrier, the host to the ore deposits. Laser multi-collector ICP-MS study of 87Sr/86Sr ratios of ore- related dolomites from Pine Point indicate two sources of Sr were present in the mineralizing system. Fluid "A" has a range in Sr isotopic values from 0.07070 to 0.7120 and is a brine derived from Middle Devonian seawater which has undergone some interaction with clastic units in the basin. Fluid "B" has is more enriched in 87Sr and has 87Sr/86Sr ratios up to up to 0.7152, values similar to those found in Canadian Shield Brines, and represents a fluid which has interacted with crystalline basement rocks. The presence of this second Sr source in the ore forming system suggests that sulfide deposition at Pine Point occurred as a result of fluid mixing.

  6. Detailed record of the Neogene Sr isotopic evolution of seawater from DSDP Site 590B. [Deep Sea Drilling Project

    SciTech Connect

    DePaolo, D.J.

    1986-02-01

    A detailed study of strontium isotope variations in Neogene marine carbonate sediments from Deep Sea Drilling Project Site 590B, using techniques that allow the /sup 87/Sr//sup 86/Sr ratio to be determined to better than +/- 0.000 01, gives a high-resolution record of the Sr isotopic evolution of seawater. The data show that the rate of change of the marine /sup 87/Sr//sup 86/Sr ratio has varied significantly even on time scales as short as 1 m.y. Periods of particularly rapid growth appear to follow major marine regressions and probably reflect an increase in the delivery of radiogenic Sr from the continents coupled with a decreased submarine carbonate dissolution rate (greater carbonate compensation depth). Periods of relatively slowly changing /sup 97/Sr//sup 86/Sr follow major marine transgressions. On the basis of correlations with the marine oxygen isotope record and the times of major continental glacier growth, it is inferred that the effects of sea-level variations are modified by climatic factors that affect the intensity of continental weathering and runoff. The effects of sea-floor generation rate variations are not discernible for the Neogene. The maximum attainable stratigraphic resolution using Sr isotopes is between 0.1 and 2 m.y. for this time period. 24 references.

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

    NASA Astrophysics Data System (ADS)

    Dolejš, David; Bendl, Jiří; Štemprok, Miroslav

    2016-10-01

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

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

    NASA Astrophysics Data System (ADS)

    Dolejš, David; Bendl, Jiří; Štemprok, Miroslav

    2016-03-01

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

  9. Delineation of groundwater flow paths using hydrochemical and strontium isotope composition: A case study in high arsenic aquifer systems of the Datong basin, northern China

    NASA Astrophysics Data System (ADS)

    Xie, Xianjun; Wang, Yanxin; Ellis, Andre; Su, Chunli; Li, Junxia; Li, Mengdi; Duan, Mengyu

    2013-01-01

    SummaryStrontium isotopic compositions and major ion chemistry were used to delineate flow paths in an arsenic affected groundwater flow system in the Datong basin, China. Total of 28 samples including one spring and one river water were collected for major ions and strontium isotopic compositions and concentration analysis. The ion ratios indicate that dissolution of silicates and carbonates is the dominant geochemical process controlling the hydrochemistry of groundwater from two recharge areas at the basin margins, while the water chemistry in the center of the basin is affected by the dissolution of evaporites (including gypsum and halite). Groundwater from eastern and western margin areas have relatively high 87Sr/86Sr values ranging from 0.72114 to 0.72604 and from 0.71119 to 0.71151, which are consistent with expected values for groundwater dominantly affected by dissolution of silicates. However, in the discharge area, the groundwater samples had lower 87Sr/86Sr values and varied between 0.71016 and 0.71753. The contour map of δ87Sr in groundwater shows the general tendency of decrease from the western and eastern margin areas to the discharge area. The plot of 87Sr/86Sr vs. Sr/Na indicates that interactions between Quaternary aquifer sediment and groundwater in the recharge areas along the flow paths control the hydrochemistry and strontium isotopic compositions of groundwater. By contrast, groundwater samples from the discharge area are plotted on the mixing line, indicating that mixing of groundwater from recharge area with low 87Sr/86Sr values groundwater could be the controlling factor on their hydrochemistry and strontium isotopic compositions. Four main flow paths of groundwater were inferred from hydrochemical and isotopic data. The results of PHREEQC inverse modeling matched quite well with the results of strontium isotopic and ion compositions along the flow paths. The distribution of high arsenic groundwater in this area could be attributed to

  10. Groundwater levels and water-quality observations pertaining to the Austin Group, Bexar County, Texas, 2009-11

    USGS Publications Warehouse

    Banta, J.R.; Clark, A.K.

    2012-01-01

    In general, the water-quality data indicated that the samples were representative of a calcium carbonate dominated system. The major ion chemistry and relations between magnesium to calcium molar ratios and 87Sr/86Sr isotopic ratios of samples collected from sites H and I indicated that the groundwater from these sites was most geochemically similar to groundwater collected from site B (State well AY-68-36-134), which is representative of groundwater in the Edwards aquifer. Of the sites sampled in this study, there appears to be varying hydrologic connectivity between groundwater from wells completed in the Austin Group and the Edwards aquifer.

  11. Precise timing and rate of massive late Quaternary soil denudation

    NASA Astrophysics Data System (ADS)

    Cooke, M. Jennifer; Stern, Libby A.; Banner, Jay L.; Mack, Lawrence E.; Stafford, Thomas W., Jr.; Toomey, Rickard S., III

    2003-10-01

    Strontium isotopes are a unique tool to study soil-erosion dynamics. Changes in Sr isotope ratios (87Sr/86Sr) provide a record of late Quaternary landscape denudation of the Edwards Plateau of central Texas, United States. The use of Sr isotopes as a tracer for soil erosion is based on the observation that, in central Texas, the 87Sr/86Sr ratio of soil correlates with soil thickness. Plants and animals express the 87Sr/86Sr ratio of exchangeable Sr in the soil. Therefore, we use changes in Sr isotope ratios through a well-dated stratigraphic sequence of fossil plants and animals in Hall's Cave, Kerr County, Texas, as a proxy for temporal changes in soil thickness. By using this record we are able to characterize late Quaternary climate-driven soil-erosion dynamics on the Edwards Plateau. We find that continuous erosion removed at least 180 cm of soil at a constant minimum rate of 11 cm/k.y.; this continuous phase of erosion ended ca. 5 ka. The Sr isotope record of soil erosion is consistent with late Quaternary environmental change in central Texas that has been independently modeled by using local and regional climate records. However, the rate of this climate-driven soil-erosion event was an order of magnitude slower than recent soil erosion caused by human land use. These results link erosion to century- to millennial-scale climate change and are cautionary evidence that even greater landscape degradation may result from coincident climatic variability and anthropogenic influences.

  12. Paleoproterozoic mantle enrichment beneath the Fennoscandian Shield: Isotopic insight from carbonatites and lamprophyres

    NASA Astrophysics Data System (ADS)

    Woodard, Jeremy; Huhma, Hannu

    2015-11-01

    The isotope geochemistry of carbonatite from Naantali, southwest Finland as well as lamprophyres from North Savo, eastern Finland and the NW Ladoga region, northwest Russia has been investigated. These Paleoproterozoic dykes represent melting of an enriched mantle source spread over a ~ 96,000 km2 area within the Fennoscandian Shield and intruded during post-collisional extension. The carbonatites have εNd(T) ranging from -0.8 to + 0.4, while lamprophyres have εNd(T) between -0.8 and + 0.3. 87Sr/86Sr ratios from the primary carbonatite samples from Naantali form a tight cluster between 0.70283 and 0.70303. For the lamprophyres, 87Sr/86Sr ratios range from 0.70327-0.70339 from NW Ladoga and 0.70316-0.70327 from North Savo. These characteristics are consistent with derivation from an enriched mantle showing an EMII trend, formed when sediments of mixed Archean and Proterozoic provenance were recycled back into the mantle via subduction during the preceding Svecofennian orogeny. Linear mixing of these subducted sediments and depleted mantle shows that a multistage process of enrichment is required to produce the observed isotope compositions. Batch melting of the subducted sediment first generated hydrous alkaline silicate melt, which crystallised as mica- and amphibole-rich veins in the mantle wedge. Continued melting of the subducted material under higher P-T conditions produced carbonatite melt, which infiltrated preferentially into this vein network. Assuming the silicate melt exerts greater influence on 87Sr/86Sr ratios while the carbonatite more greatly affects 143Nd/144Nd ratios, the model predicts significant regional variation in the silicate metasomatism with more consistent carbonatite metasomatism throughout the Fennoscandian subcontinental lithospheric mantle. The subducted sediments were likely also rich in organic matter, resulting in highly negative δ13C in mantle carbonates. The model predicts a higher content of organic carbon in the sediments in

  13. Implications for post-comminution processes in subglacial suspended sediment using coupled radiogenic strontium and neodymium isotopes

    NASA Astrophysics Data System (ADS)

    Clinger, Anna E.; Aciego, Sarah M.; Stevenson, Emily I.; Arendt, Carli A.; Robbins, Mark J.

    2016-04-01

    Enhanced physical weathering rates in subglacial systems promote high levels of comminution, transport, and deposition of fine-grained sediment within the subglacial drainage network. The impact of shifts in sediment loads from variations in meltwater flux, and their effects on downstream ecosystems, remains poorly quantified and places a fundamental importance on our ability to characterize subglacial depositional environments. Here, for the first time, we assess the seasonal evolution of the subglacial suspended sediment using coupled radiogenic strontium (87Sr/86Sr) and neodymium (143Nd/144Nd) isotopic ratios with elemental ratios and in situ measurements. Weathering rates in fluvial and riverine systems have been traditionally assessed using radiogenic isotopic tracers: 143Nd/144Nd ratios relate to the crustal age whereas 87Sr/86Sr ratios relate to age and preferential mineral dissolution. Thus relative shifts in these ratios will allow us to characterize distinct sediment transport networks. We apply this technique to the Lemon Creek Glacier (LCG), Alaska, USA, and to the Athabasca Glacier (AG), Alberta, CA. At the LCG, the 143Nd/144Nd values range from εNd of - 4.6 (0.9) to - 8.7 (0.2), which suggests a poorly mixed sediment flux. However, the greatest period of variability may correlate with the drainage of a supraglacial lake and suggests caution should be exerted in time-scale 143Nd/144Nd provenance studies that may be affected by climatic disturbances. In contrast, limited variation is observed within the AG 143Nd/144Nd seasonal record. A consistent, direct relation between the Rb/Sr elemental ratio and the 87Sr/86Sr ratio proves interesting as it enables us to unravel incongruent weathering trends in the radiogenic Sr record. Correlation between the 87Sr/86Sr and total discharge suggests that the process is partially controlled by mantling of the bedrock, which can be detected using post-comminution ages. While the subglacial structure may be enabled by

  14. The halogen (F, Cl, Br, I) and H2O systematics of Samoan lavas: Assimilated-seawater, EM2 and high-3He/4He components

    NASA Astrophysics Data System (ADS)

    Kendrick, Mark A.; Jackson, Matthew G.; Hauri, Erik H.; Phillips, David

    2015-01-01

    The Samoan mantle plume samples two or more mantle components including an extreme EM2 composition with 87Sr/86Sr > 0.720 and a primitive component with high 3He/4He. The high 87Sr/86Sr melts have a unique potential to constrain the composition of the EM2 mantle end-member that is commonly attributed to subduction recycling. However, a previous study of H2O, CO2, S, F and Cl in Samoan glasses was hampered by the presence of unresolved assimilated sea water. The current study builds on the earlier work by extending the volatile database to include the trace halogens Br and I, and reporting new volatile data for additional glasses with 87Sr/86Sr up to 0.7125 and 3He/4He up to 15 Ra (Ra is the atmospheric 3He/4He ratio of 1.39 ×10-6). The selected glasses with MgO of 4.0 to 6.5 wt.% have CO2 concentrations of 4 to 200 ppm that reflect degassing of CO2 on the seafloor. The glasses contain 0.7-1.9 wt.% H2O, 880-1870 ppm F, 490-1790 ppm Cl, 1.9-7.2 ppm Br, 19-130 ppb I and 0.6-1.7 wt.% K. Correlations between the concentrations of these elements suggest the melts retain H2O concentrations close to pre-degassing values and demonstrate the melts have been variably affected by assimilation of seawater-derived brines. The brines are indicated to have had salinities of 55 ± 15 wt.% salt, F/Cl ratios close to seawater (e.g. <0.0001), Br/Cl ratios ∼ 40% higher than seawater, and I/Cl ratios ten times the seawater value. It is calculated the melts assimilated brine fractions of 0 to 0.45 wt.%, which contributed up to ∼30% of the total H2O and up to ∼70% of the total Cl in the melts. After accounting for the effects of brine assimilation, the Samoan melts are suggested to have a fairly constant magmatic Cl/K of 0.05 ± 0.2, which is lower than the median MORB value. Assimilation-corrected H2O/Ce values are not correlated with 87Sr/86Sr, but the sample with the highest 87Sr/86Sr of 0.7125 has an assimilation-corrected H2O/Ce of 83 ± 3, that is significantly lower than

  15. Formation waters from Mississippian-Pennsylvanian reservoirs, Illinois basin, USA: Chemical and isotopic constraints on evolution and migration

    SciTech Connect

    Stueber, A.M. ); Walter, L.M.; Huston, T.J. ); Pushkar, P. )

    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 evaporation 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.

  16. Chemical and isotopic studies of granitic Archean rocks, Owl Creek Mountains, Wyoming: Geochronology of an Archean granite, Owl Creek Mountains, Wyoming

    SciTech Connect

    Hedge, C.E.; Simmons, K.R.; Stuckless, J.S.

    1986-01-01

    Rubidium-strontium analyses of whole-rock samples of an Archean granite from the Owl Creek Mountains, Wyo., indicate an intrusive age of 2640 {plus minus} 125 Ma. Muscovite-bearing samples give results suggesting that these samples were altered about 2300 Ma. This event may have caused extensive strontium loss from the rocks as potassium feldspar was altered to muscovite. Alteration was highly localized in nature as evidence by unaffected rubidium-strontium mineral ages in the Owl Creek Mountains area. Furthermore, the event probably involved a small volume of fluid relative to the volume of rock because whole-rock {delta}{sup 18}O values of altered rocks are not distinct from those of unaltered rocks. In contrast to the rubidium-strontium whole-rock system, zircons from the granite have been so severely affected by the alteration event, and possibly by a late-Precambrian uplift event, that the zircon system yields little usable age information. The average initial {sup 87}Sr/{sup 86}Sr (0.7033 {plus minus} 0.0042) calculated from the isochron intercept varies significantly. Calculated initial {sup 87}Sr/{sup 86}Sr ratios for nine apparently unaltered samples yield a range of 0.7025 to 0.7047. These calculated initial ratios correlate positively with whole-rock {delta}{sup 18}O values; and, therefore, the granite was probably derived from an isotopically heterogeneous source. The highest initial {sup 87}Sr/{sup 86}Sr ratio is lower than the lowest reported for the metamorphic rocks intruded by the granite as it would have existed at 2640 Ma. Thus, the metamorphic sequence, at its current level of exposure, can represent no more than a part of the protolith for the granite.

  17. Boron and strontium isotope compositions of groundwater from the La Paz arid coastal aquifer, Baja California Sur, Mexico

    NASA Astrophysics Data System (ADS)

    Mahlknecht, Jürgen; Rosner, Martin; Meixner, Anette

    2016-04-01

    In groundwater studies boron and strontium isotopic compositions can be used to identify natural and anthropogenic sources as well as processes related to groundwater recharge, flow and mixing. The La Paz arid costal aquifer in Baja California Sur, Mexico, is the most important source of drinking and irrigation water for La Paz area and suffers from anthropogenic contamination and intensive exploitation of the aquifer causing seawater intrusion and general groundwater abatement. The relatively un-radiogenic 87Sr/86Sr isotope ratios of the La Paz groundwater range in a narrow field between 0.7054 and 0.7062. In contrast to strontium the boron isotope composition displays a large variability between +27 and +55 permil d11B. The relatively low 87Sr/86Sr ratios of the La Paz groundwater highlight a significant contribution of strontium derived from local terrestrial sediments and igneous rocks with known 87Sr/86Sr ratios between 0.705 and 0.7035. The large variability of d11B values indicate that multiple sources and processes determine the boron isotope composition of La Paz groundwater. Rainwater (high d11B), seawater (~+40 permil) due to seawater intrusions, wastewater (low to medium d11B) and boron derived from the local geology (low to medium d11B) explain most of the observed groundwater d11B variability. However, d11B values higher than modern seawater point to significant boron isotope fractionation by preferential absorption of 10B onto clay minerals during the evolution of some groundwater samples. Due to low boron concentrations in rainwater a significant contribution of 11B-rich rainwater (>+40 permil) on the La Paz groundwater is unlikely.

  18. Diagenesis of an upper Devonian carbonate-evaporite sequence: Birdbear Formation, southern interior plains, Canada

    SciTech Connect

    Whittaker, S.G.; Mountjoy, E.W.

    1996-09-01

    The Frasnian Birdbear (Nisku) Formation is a carbonate-evaporite succession formed on a shallow restricted shelf along the eastern side of the Western Canada Sedimentary Basin. Low {delta}{sup 13}C values of the shelf limestones and dolostones (1%--5%) relative to coeval open marine settings reflect the restricted paleoenvironment of the shelf. Limestones are present only in the eastern part of the study area, and were altered by meteoric and burial diagenesis and do not retain marine {delta}{sup 18}O values. {delta}{sup 18}O values of replacement dolomites have limited range ({minus}3%--5%) and may indicate dolomitization by hypersaline marine waters having low {delta}{sup 18}O values. {sup 87}Sr/{sup 86}Sr ratios of the replacement dolomites are variable (0.7082--0.7085), but also suggest that reflux of Late Devonian seawater, possibly Famennian, was the principal dolomitizing mechanism in the Birdbear shelf. Most bedded anhydrites have {delta}{sup 34}S values (22% to 24% CDT) and {sup 87}Sr/{sup 86}Sr ratios (ca. 0.7081) that record Frasnian seawater. Dissolution and reprecipitation of sedimentary sulfates resulted in sulfate cements having up to 2% higher {delta}{sup 34}S values and slightly higher {sup 87}Sr/{sup 86}Sr ratios (ca. 0.7083). Fluids associated with anhydrite dissolution may have been derived from the overlying Famennian shelf. Late diagenetic cements in the Birdbear Shelf precipitated during the Late Cretaceous and early Tertiary during maximum burial from hot, evolved residual evaporitic brines. Residual evaporitic brines that originated on the shallow eastern Upper Devonian shelves were likely important agents of diagenesis throughout the basin.

  19. Paleo-Asian oceanic subduction-related modification of the lithospheric mantle under the North China Craton: Evidence from peridotite xenoliths in the Datong basalts

    NASA Astrophysics Data System (ADS)

    Wang, Chengyuan; Liu, Yongsheng; Min, Ning; Zong, Keqing; Hu, Zhaochu; Gao, Shan

    2016-09-01

    In-situ major and trace elements and Sr isotopic compositions of peridotite xenoliths of the Datong Quaternary alkaline basalt were analyzed to evaluate the influences of the southward subduction of the Paleo-Asian oceanic plate (PAOP) on the lithospheric mantle transformation of the North China Craton (NCC). These peridotite xenoliths including spinel harzburgites and lherzolites were classified into three groups. The type 1 peridotites have the lowest temperatures (961-1007 °C). Clinopyroxenes in these peridotites exhibit LREE-depleted REE patterns and have the lowest 87Sr/86Sr ratios of 0.70243-0.70411. The type 2 and 3 peridotites show higher temperatures (1017-1022 °C). Clinopyroxenes in the type 2 peridotite have V-shaped REE patterns and relatively higher 87Sr/86Sr ratios of 0.70418-0.70465. Clinopyroxenes in the type 3 peridotite have concave-downward REE patterns and unusually high 87Sr/86Sr ratios of 0.70769-0.70929. Carbonatitic veinlets are found in the type 1 peridotites. They show steep LREE-enriched REE patterns with enrichment in LILE and depletion in HFSE, and have the highest 87Sr/86Sr ratios of 0.71145-0.71285. The mineral chemistries and modal calculations suggest that the protolith of these peridotites experienced a variable degree of partial melting. The type 2 and 3 peridotites sampled from deeper depth experienced latter cryptic carbonatitic metasomatism. The carbonatitic veinlets have generally consistent trace element patterns and Sr isotopic ratios with the calculated melts equilibrated with clinopyroxenes in the type 3 peridotite, which may represent the percolated carbonatitic melt quickly solidified in the relatively cold and shallow mantle. The remarkable negative Eu anomalies (0.37-0.61) and highly radiogenic Sr isotopic compositions of the calculated metasomatic agents preclude indicate melt derived from carbonated peridotite or carbonated eclogite but point to a crustal sedimentary origin. Considering the tectonic setting and

  20. Diffusive isotopic contamination of mafic magma by coexisting silicic liquid in the muskox intrusion.

    PubMed

    Stewart, B W; Depaolo, D J

    1992-02-01

    Shifts in (87)Sr/(86)Sr and (143)Nd/(144)Nd ratios measured in cumulates from the upper levels of the Muskox mafic intrusion indicate that isotopic and bulk chemical exchange were decoupled across a mafic-silicic liquid interface during crystallization of the intrusion. Modeling of diffusive exchange between liquid layers demonstrates that isotopic compositions of silicate liquids in layered magma chambers may be strongly affected by this process on time scales of 10(3) to 10(4) years. Diffusive contamination can be used to place constraints on the physical processes and time scales of magmatic systems.

  1. Diffusive isotopic contamination of mafic magma by coexisting silicic liquid in the muskox intrusion.

    PubMed

    Stewart, B W; Depaolo, D J

    1992-02-01

    Shifts in (87)Sr/(86)Sr and (143)Nd/(144)Nd ratios measured in cumulates from the upper levels of the Muskox mafic intrusion indicate that isotopic and bulk chemical exchange were decoupled across a mafic-silicic liquid interface during crystallization of the intrusion. Modeling of diffusive exchange between liquid layers demonstrates that isotopic compositions of silicate liquids in layered magma chambers may be strongly affected by this process on time scales of 10(3) to 10(4) years. Diffusive contamination can be used to place constraints on the physical processes and time scales of magmatic systems. PMID:17756951

  2. High throughput Sr isotope analysis using an automated column chemistry system

    NASA Astrophysics Data System (ADS)

    Mackey, G. N.; Fernandez, D.

    2011-12-01

    A new method has been developed for rapidly measuring 87Sr/86Sr isotope ratios using an autosampler that automates column chemistry for Sr purification. The autosampler, a SC2 DX with FAST2 valve block, produced by Elemental Scientific, Inc., utilizes a pair of six-way valves, a vacuum, and a peristaltic pump to load a sample from an autosampler tube onto the Eichrom Sr Resin in the separation column. The autosampler then elutes the sample from the column directly into the spray chamber of the mass spectrometer. Measurements are made on a Thermo-Finnigan Neptune ICP-MS. Sample-blank pairs require approximately 30 minutes for analysis. Normal throughput for the system is 24 samples and 11 standards per day. Adjustment of the pump speed allows for rapid loading of the column followed by a 3-minute data acquisition period with no fractionation of the Sr being eluted from the column. All data are blank-, interference-, and normalization-corrected online using 86Sr/88Sr = 0.1194. Analytical precision on a typical 66 ng/g analysis is ±0.00003 (2σ SE). Reproducibility of the SRM987 Sr standard (66 ng/g) over the course of a typical sequence is ±0.00004 (2σ SD, n=11). For comparison, offline column separation of the SRM987 Sr standard (66 ng/g) was conducted and measured using the same instrument method, yielding a reproducibility of ±0.00004 (2σ SD, n=7). The long-term average of the SRM987 standard (10-200 ng/g) utilizing the online column chemistry method is 0.71027 ± 0.00010 (2σ SD, n=239). A small memory effect has been measured by alternating spiked samples (87Sr/86Sr = 0.67465) with the SRM987 standard. The bias measured in this test (87Sr/86Sr +0.00006) slightly exceeds the 2σ standard reproducibility for a typical run with sample and standard concentrations near 66 ng/g, but is within the 2σ long-term reproducibility of the method. The optimal concentration range for the offline column chemistry system is 50-250 ng/g Sr. Sample concentrations above 250

  3. Strontium isotope tracking of groundwater-CO2 interactions in Chimayo, New Mexico, and implications for carbon storage in geologic formations

    NASA Astrophysics Data System (ADS)

    Gardiner, J.; Stewart, B. W.; Capo, R.; Hakala, J.

    2009-12-01

    James Gardiner1, Brian Stewart1, Rosemary Capo1, J. Alexandra Hakala2 1Department of Geology and Planetary Sciences, University of Pittsburgh 2National Energy Technology Laboratory, Pittsburgh, PA The storage of carbon dioxide in geologic formations requires sensitive monitors of the geochemical and mineralogical interactions of storage units, their formation waters, and associated aquifers potentially affected by subsurface CO2. High CO2 subsurface environments can serve as natural analogues for conditions following CO2 injection and provide sites to develop and optimize geochemical tools that can characterize subsurface reactions and identify and track brine and groundwater interactions. Wells in Chimayó, NM tap groundwater from the Tesuque sandstone aquifer, which is crosscut by faults that act as conduits for naturally occurring, deeply sourced CO2. This provides an opportunity for geochemical and isotopic characterization of groundwaters potentially influenced by interaction with CO2. Well waters in the region have 87Sr/86Sr ratios ranging from 0.7176 for CO2-charged brackish water to 0.7098 for a low-TDS groundwater, making the Sr isotope system a potentially sensitive tracer for groundwater-rock interactions. Preliminary strontium isotopic and geochemical data lead to the following observations: (1) Strontium isotope ratios and Sr concentrations in groundwaters sampled within the basin suggest a complex mixing between deep- and shallow-sourced waters, possibly combined with reactions of aquifer carbonate cement or local limestone. (2) Adjacent wells with identical 87Sr/86Sr but significantly different CO2 and alkaline earth concentrations imply CO2 migration from depth into a shallow aquifer, followed by dissolution of carbonate cement. (3) Sr isotope mixing models, when used in conjunction with other geochemical data, can be a strong indicator of decoupling between CO2 and its carrier fluid. Conservative isotope tracers such as 87Sr/86Sr could be an

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

    NASA Astrophysics Data System (ADS)

    Weber, Peter K.; Bacon, Charles R.; Hutcheon, Ian D.; Ingram, B. Lynn; Wooden, Joseph L.

    2005-03-01

    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 (2σ) 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 μm laterally and 2 μm 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.

  5. The influence of methane seeps on the paleoecology and geochemistry of the Western Interior Seaway of North America: evidence from C and Sr isotopes in well-preserved shells of a seep fauna from the Upper Cretaceous (Campanian) Pierre Shale

    NASA Astrophysics Data System (ADS)

    Cochran, J. K.; Landman, N. H.; Harries, P. J.; Larson, N. L.; Garb, M. P.; Klofak, S. M.; Myers, C.; Brezina, J.

    2011-12-01

    Methane seep deposits are common in the Upper Cretaceous Pierre Shale of the U.S. Western Interior. They contain a rich fauna including ammonites (Baculites, Hoploscaphites, Didymoceras, Placenticeras, Solenoceras), bivalves (Lucina), gastropods, sponges, and crinoids. In an effort to understand the environment of these systems and their influence on the Seaway, we have examined a seep from the upper Campanian Didymoceras cheyennense Zone (~74.7 Ma) in Custer County, South Dakota (USA), in which the molluscs retain their original shell microstructure. Values of δ13C in the micritic limestone of the seep range from -11% to -47%, and the light values confirm the impact of anaerobic oxidation of methane on the isotopic composition of the dissolved inorganic carbon reservoir. Light δ13C values also are observed in well-preserved specimens of the ammonites Hoploscaphites (-1.2% to -7.6%) and Baculites (-0.6% to -14%). These values are significantly lighter than those measured in non-seep specimens. In a few specimens of Baculites, light δ13C values were observed through ontogeny. We conclude that the ammonite shells incorporated isotopically light dissolved inorganic carbon derived from seep methane and that these mobile animals were living in close proximity to the vent fluids. The 87Sr/86Sr ratio is also elevated in the limestone core and well-preserved shells of ammonites (0.707693 - 0.707728) compared with the coeval marine value (0.707658), suggesting that the seep fluids are imprinted with a radiogenic Sr signature, perhaps derived from isotopic exchange with granitic deposits at depth. In contrast with the pattern seen in δ13C, samples of D. cheyennense collected away from the seep show 87Sr/86Sr ratios that are comparable to the seep values. Thus the source of Sr from methane seeps may have been sufficient to imprint itself on the 87Sr/86Sr of the Western Interior Seaway at the time.

  6. Isotope geology of the bakircay porphyry copper prospect, northern turkey

    NASA Astrophysics Data System (ADS)

    Taylor, R. P.

    1981-10-01

    Isotopic data for the Bakircay granodiorite porphyry, MediaObjects/126_2005_BF01798964_f1.tif give a Late Eocene age for the development of the porphyry copper system. They suggest a close temporal and genetic relationship between igneous and hydrothermal activity, and indicate that magmatic-hydrothermal fluids produced potassic alteration and that meteoric fluids enriched in radiogenic87Sr were responsible for propylitic alteration. The granodiorite porphyry is petrologically similar to porphyry copper-related intrusions from island arc and continental margin settings, which form a group with initial87Sr/86Sr ratios of less than 0. 7043, representing magmas produced in tectonic environments lacking any important component of old (i. e. Precambrian) continental material.

  7. The Island Arcs as a Major Source of Mantellic Sr to the Ocean: Tectonic Control over Seawater Chemistry and Climate

    NASA Astrophysics Data System (ADS)

    Louvat, P.; Allegre, C. J.; Meynadier, L.

    2005-12-01

    The evolution of 87Sr/86Sr in the Cenozoic ocean has been the subject of famous and vivid controversies between the BLAG model1 and Raymo's one2. No clear winner! Recently the question has been worsened because recent estimates of the hydrothermal flux at ridge crest3, 4, 5 and of the low-temperature oceanic crust weathering flux6 have shown that these fluxes are not enough to balance the continental radiogenic input to give 0.70917 (present-day seawater 87Sr/86Sr). We have re-examined this problem using both Sr and Nd isotopic budgets. Seawater 143Nd/144Nd isotopic ratio varies from one ocean to another as a consequence of its short residence time. For each ocean we can calculate the Nd contributions from continental (rivers) and mantellic sources. Since ridge crests cannot be the mantle-like source for Nd, this source is identified as the island arc and OIB weathering, in agreement with the observation by Goldstein and Hemming7. This approach leads us to examine the possibility of the same island arc origin for the missing mantle-like seawater Sr. The classical approach to the budget of water entering the ocean is to consider the river water fluxes as established by hydrological survey statistics. But these fluxes are too small, as they do not include the underground water flows, which are particularly important for volcanic terrains8. A budget calculation based on mean surface area, mean water fluxes and mean Sr concentrations in rivers and springs demonstrates island arc and OIB weathering is a sufficient source of mantellic Sr to the ocean to match the seawater 87Sr/86Sr budget. This result has a fundamental consequence on the explanation of the seawater 87Sr/86Sr evolution during the Cenozoic. Indeed, when a continental collision occurs a large portion of island arcs is eliminated. Thus the increase in the contribution of radiogenic 87Sr/86Sr from continental weathering and the decrease of the mantle contribution via island arc weathering are tectonically and

  8. The origin and mechanisms of salinization of the Lower Jordan River

    USGS Publications Warehouse

    Farber, E.; Vengosh, A.; Gavrieli, I.; Marie, A.; Bullen, T.D.; Mayer, B.; Holtzman, R.; Segal, M.; Shavit, U.

    2004-01-01

    The chemical and isotopic (87Sr/86Sr, ??11B, ??34Ssulfate, ??18Owater, ??15Nnitrate) compositions of water from the Lower Jordan River and its major tributaries between the Sea of Galilee and the Dead Sea were determined in order to reveal the origin of the salinity of the Jordan River. We identified three separate hydrological zones along the flow of the river: (1) A northern section (20 km downstream of its source) where the base flow composed of diverted saline and wastewaters is modified due to discharge of shallow sulfate-rich groundwater, characterized by low 87Sr/86Sr (0.7072), ??34Ssulfate (-2???), high ??11B (???36???), ??15Nnitrate (???15???) and high ??18Owater (-2 to-3???) values. The shallow groundwater is derived from agricultural drainage water mixed with natural saline groundwater and discharges to both the Jordan and Yarmouk rivers. The contribution of the groundwater component in the Jordan River flow, deduced from mixing relationships of solutes and strontium isotopes, varies from 20 to 50% of the total flow. (2) A central zone (20-50 km downstream from its source) where salt variations are minimal and the rise of 87Sr/86Sr and SO4/Cl ratios reflects predominance of eastern surface water flows. (3) A southern section (50-100 km downstream of its source) where the total dissolved solids of the Jordan River increase, particularly during the spring (70-80 km) and summer (80-100 km) to values as high as 11.1 g/L. Variations in the chemical and isotopic compositions of river water along the southern section suggest that the Zarqa River (87Sr/86Sr???0.70865; ??11B???25???) has a negligible affect on the Jordan River. Instead, the river quality is influenced primarily by groundwater discharge composed of sulfate-rich saline groundwater (Cl-=31-180 mM; SO4/Cl???0.2-0.5; Br/Cl???2-3??10-3; 87Sr/86Sr???0.70805; ??11B???30???; ??15Nnitrate ???17???, ??34Ssulfate=4-10???), and Ca-chloride Rift valley brines (Cl-=846-1500 mM; Br/Cl???6-8??10-3; 87Sr/86Sr???0

  9. The ubiquitous nature of accessory calcite in granitoid rocks: Implications for weathering, solute evolution, and petrogenesis

    USGS Publications Warehouse

    White, A.F.; Schulz, M.S.; Lowenstern, J. B.; Vivit, D.V.; Bullen, T.D.

    2005-01-01

    Calcite is frequently cited as a source of excess Ca, Sr and alkalinity in solutes discharging from silicate terrains yet, no previous effort has been made to assess systematically the overall abundance, composition and petrogenesis of accessory calcite in granitoid rocks. This study addresses this issue by analyzing a worldwide distribution of more than 100 granitoid rocks. Calcite is found to be universally present in a concentration range between 0.028 to 18.8 g kg-1 (mean = 2.52 g kg-1). Calcite occurrences include small to large isolated anhedral grains, fracture and cavity infillings, and sericitized cores of plagioclase. No correlation exists between the amount of calcite present and major rock oxide compositions, including CaO. Ion microprobe analyses of in situ calcite grains indicate relatively low Sr (120 to 660 ppm), negligible Rb and 87Sr/86Sr ratios equal to or higher than those of coexisting plagioclase. Solutes, including Ca and alkalinity produced by batch leaching of the granitoid rocks (5% CO2 in DI water for 75 d at 25??C), are dominated by the dissolution of calcite relative to silicate minerals. The correlation of these parameters with higher calcite concentrations decreases as leachates approach thermodynamic saturation. In longer term column experiments (1.5 yr), reactive calcite becomes exhausted, solute Ca and Sr become controlled by feldspar dissolution and 87Sr/ 86Sr by biotite oxidation. Some accessory calcite in granitoid rocks is related to intrusion into carbonate wall rock or produced by later hydrothermal alteration. However, the ubiquitous occurrence of calcite also suggests formation during late stage (subsolidus) magmatic processes. This conclusion is supported by petrographic observations and 87Sr/86Sr analyses. A review of thermodynamic data indicates that at moderate pressures and reasonable CO2 fugacities, calcite is a stable phase at temperatures of 400 to 700??C. Copyright ?? 2005 Elsevier Ltd.

  10. Rb sbnd Sr isotopic analysis of fluid inclusions in quartz: Evaluation of bulk extraction procedures and geochronometer systematics using synthetic fluid inclusions

    NASA Astrophysics Data System (ADS)

    Pettke, Thomas; Diamond, Larryn W.

    1995-10-01

    Analysis of Rb sbnd Sr isotopic and elemental signatures of fluid inclusions is technically demanding, but it offers enormous potential in elucidating the timing, sources, and geochemical reaction paths of fluids in the Crust. Fluid inclusions of known isotopic and elemental ratios have been synthesized in quartz to serve as control samples. With these standards, two previously used fluid extraction procedures for bulk quartz samples have been evaluated and improved: crushing in a mortar followed by leaching and thermal decrepitation followed by leaching. Our experiments on quartz show that 87Sr/ 86Sr analysis is straightforward using both methods, regardless of the leaching solution employed. However, analysis of accurate 87Rb/ 86Sr ratios is not trivial. Leaching with pure water is only 93% efficient and yields elevated ratios owing to failure to inhibit surface adsorption of Sr. Leaching with a La 3+-doped acid solution solves this problem; it is 99.7% efficient and yields accurate ratios. Crushing is the only fluid liberation method which delivers the correct 87Rb/ 86Sr values. In contrast, thermal decrepitation yields 87Rb/ 86Sr ratios which are quite reproducible, but exclusively incorrect. If inert sample containers are used, falsely elevated ratios are obtained at all decrepitation temperatures due to three concurrent extraction artefacts. However, if silica glass tubes are used, reaction of Rb with the glass at temperatures above ˜ 500°C falsely lowers the 87Rb/ 86Sr signatures. We, therefore, suspect all published isotopic analyses of fluid inclusions obtained by thermal decrepitation to be in error. The trace contents of Rb and Sr in the host quartz crystals are measurable and have markedly different Rb/Sr ratios compared to the hydrothermal parent fluid. Thus analyses of leachates and host-mineral residues by the crushing method allow accurate ages to be calculated with certainties of an order which are useful for geochronology. Since fluid extraction

  11. Mantle heterogeneities beneath the South Atlantic: a Nd sbnd Sr sbnd Pb isotope study along the Mid-Atlantic Ridge (3°S-46°S)

    NASA Astrophysics Data System (ADS)

    Fontignie, Denis; Schilling, Jean-Guy

    1996-07-01

    We report on 55 Nd and Sr isotope analyses of Mid-Atlantic Ridge (MAR) basalt glasses from 3°S to 46°S, using the same samples on which Pb and He isotope ratios were reported earlier (Hanan et al. [1] and Graham et al. [2]). Eighteen new Pb, Sr, and Nd isotope analyses are also reported on basalt glasses from 17 stations from the same region. 87Sr 86Sr ratios range from 0.70212 to 0.70410 and 143Nd 144Nd from 0.51285 to 0.51331. The along-ridge long wavelength 87Sr 86Sr variation delineated by light-REE depleted basalts increases progressively southward toward Tristan da Cunha. Short wavelength, spike-like, positive 87Sr 86Sr anomalies composed of light-REE enriched basalts are found opposite the Tristan, St. Helena, and Circe (Ascension) hotspots (as for the Pb isotopes). The short and long wavelength 143Nd 144Nd variations anti-correlate with those of 87Sr 86Sr . The 17 new Pb isotope analyses confirm both the short and long wavelength trends previously reported by Hanan et al. [1]. These spatial variations, as well as the variations in Nd sbnd Sr sbnd Pb isotopic space fully confirm the mantle plume-ridge interaction model and upper mantle mixing conditions beneath the South Atlantic inferred previously on the basis of Pb isotopic data only (Hanan et al. [1]). However, in Nd sbnd Sr isotopic subspace the Circe and the St. Helena mixing vector are not distinguishable. The short wavelength Nd sbnd Sr sbnd Pb sbnd He anomalies suggest recent lateral sublithospheric channeled flows from these off-ridge plumes to the migrating MAR axis. The long wavelength variations reflect a broad pollution of the asthenosphere by Pb and Sr radiogenic, isotope-rich, mantle material, which has been partly depleted of incompatible elements relatively recently. This broad pollution may be related to the partial melting and dispersion of the Tristan and St. Helena plume heads into the subcontinental asthenosphere, prior to the opening of the South Atlantic. In this two-stage model

  12. Reconstructing the oxygen isotope composition of late Cambrian and Cretaceous hydrothermal vent fluid

    NASA Astrophysics Data System (ADS)

    Turchyn, Alexandra V.; Alt, Jeffrey C.; Brown, Shaun T.; DePaolo, Donald J.; Coggon, Rosalind M.; Chi, Guoxiang; Bédard, Jean H.; Skulski, Thomas

    2013-12-01

    Oxygen isotope analyses (δ18O) of 16 quartz-epidote pairs from late Cambrian (Betts Cove and Mings Bight, Newfoundland), Ordovician (Thetford Mines, Québec, Canada) and Cretaceous (Troodos, Cyprus) ophiolites are used to calculate the δ18O of the hydrothermal fluids from which they crystallized. We combine these with 3 quartz-fluid inclusion measurements and 3 quartz-magnetite measurements from the Cambrian ophiolites to explore how the range in the δ18O of submarine hydrothermal vent fluid has varied between the late Cambrian, Cretaceous and today. The range of calculated δ18O values of vent fluid (-4 to +7.4) is larger than that of modern seafloor hydrothermal vent fluid (0 to +4). We employ two numerical models to ascertain whether this range is most consistent with changes in paleo-seawater δ18O or with changes in the reactive flow path in ancient hydrothermal systems. A static calculation of the vent fluid oxygen isotope composition as a function of the water-rock ratio suggests that in an ocean with a lower δ18O than today, the range of vent fluid δ18O should be larger. Our data, however, show little evidence that the δ18O of the ocean was much lower than the global ice-free value of -1.2. A dual porosity model for reactive flow through fractured and porous media is used to model the relative evolution of the 87Sr/86Sr and δ18O of vent fluid in contact with rock. Our 87Sr/86Sr and δ18O for Cretaceous epidotes suggest the strontium concentration of the Cretaceous oceans may have been much higher than at present. The 87Sr/86Sr and δ18O data from Cambrian epidotes are strikingly different from the younger samples, and are difficult to model unless fluid-rock interaction in the Cambrian hydrothermal systems was substantially different. It is also possible that some of the quartz-epidote veins have been reset by obduction-related metamorphism. Our data suggest that the high calcium-to-sulfate ratio in early (and Cretaceous) seawater may have affected

  13. Isotopic constraints on open system evolution of the Laacher See magma chamber (Eifel, West Germany)

    NASA Astrophysics Data System (ADS)

    Wörner, G.; Staudigel, H.; Zindler, A.

    1985-09-01

    The Laacher See phonolite tephra sequence (11,000 years B.P.) of the Quaternary East Eifel volcanic field (West Germany) represents an inverted, chemically zoned magma column. Mafic and differentiated phonolites, respectively, represent the lowermost and uppermost erupted portion of the Laacher See magma chamber. Sr and Nd isotopic compositions of whole rocks, matrices and phenocrysts have been analyzed in order to provide constraints for open versus closed system evolution of the Laacher See magma chamber. 87Sr/ 86Sr isotope ratios of mafic phonolites and their phenocrysts are slightly more radiogenic than parental East Eifel basanite magmas. Bulk rock samples show a drastic increase in 87Sr/ 86Sr from mafic towards the most differentiated compositions that were erupted from the top of the magma chamber. Glass matrix separates show a parallel, but less pronounced, increase in 87Sr/ 86Sr . Phenocrysts, in contrast, show a narrow range in 87Sr/ 86Sr with a slight, but significant, increase towards the top of the magma chamber. Phenocrysts from the uppermost portion of the magma column were not in isotopic (or chemical) equilibrium with their host matrices. 143Nd/ 144Nd isotope ratios for whole rocks, matrices, and phenocrysts fall within a restricted range similar to that of East Eifel mafic magmas. A representative suite of crustal rocks (lower crustal granulites, quartzo-feldspathic gneisses, mica schists, Devonian slates and graywacke) was also analyzed in order to permit an evaluation of possible assimilation models. Our results are consistent with chemical evolution of the zoned Laacher See magma chamber mainly through crystal fractionation accompanied by minor amounts of assimilation. Slight contamination of the magma system may have involved (a) the assimilation of gneisses (?) and mica schists during the initial stage of magma chamber evolution (basanite-mafic phonolite), (b) combined assimilation-fractional crystallization (AFC) concurrent with the second

  14. Multi-isotopes constraints on the origins and processes of groundwater salinization in coastal aquifers. Example of Recife, Northeast of Brazil

    NASA Astrophysics Data System (ADS)

    Cary, Lise; Petelet-Giraud, Emmanuelle; Bertrand, Guillaume; Kloppmann, Wolfram; Aquilina, Luc; Pauwels, Helène; Martins, Veridiana; Hirata, Ricardo; Montenegro, Suzana

    2015-04-01

    The Recife Metropolitan Region (PE, Brazil) is a typical "hot spot" illustrating the problems of southern countries on water issues inducing high pressures on water resources both on quantity and quality in the context of global social and environmental changes. This study focuses on the groundwater geochemistry in a costal multilayer aquifer and aims at investigating the sources and processes of salinization. The RMR basement is constituted by two different Precambrian blocks separated by a large lineament area. The sedimentary fillings of the two basins present different origins that can be distinguished by the Sr isotope composition. The northern deep Beberibe aquifer displays very high strontium isotope ratios with a large range of values (87Sr/86Sr = 0.7102 to 0.7233) illustrating the main continental origin of sediments whereas the southern deep Cabo aquifer showed lower 87Sr/86Sr values (87Sr/86Sr = 0.7097 to 0.7141) indicating the contribution of the marine sedimentation dating from the Atlantic opening. Although sulfate isotopes, Electric Conductivity and Cl contents indicate a clear mixing with seawater for some samples of the deep Cabo and Beberibe aquifers, all 87Sr/86Sr values are above the present-day seawater composition. This can be related to the complex local history of transgression/regression phases that induced alternatively salinisation and freshening with gains and losses of cations and Sr, together with water-rock interactions. Stable isotopes of the water molecule clearly evidence the local present day recharge especially within the surficial aquifer, whereas some samples are affected by in situ evaporation processes and/or recharge with evaporated water originating from dam used for water supply. The two deep aquifers display a high range of B concentrations (~20 to 600 µg.L-1) and B isotope composition (δ11B = 6.7 to 68.5 ‰), with the highest values known to date (63-68.5‰). This suggests multiple sources and processes affecting B

  15. Chemostratigraphies of carbon, oxygen and strontium isotopes and oxygen contents across the Precambrian-Cambrian boundary

    NASA Astrophysics Data System (ADS)

    Komiya, T.; Sawaki, Y.; Ishikawa, T.

    2007-12-01

    The Precambrian-Cambrian (PC-C) boundary is one of the most important intervals for evolution of life. However, the scarcity of well-preserved outcrops through the boundary makes it ambiguous to decode change of the surface environment and biological evolution. In south China, strata through the PC-C boundary are continuously exposed and contain many fossils, suitable for study of environmental and biological change. In addition, we conducted excavations at four sites of Three Gorge area to obtain continuous and fresh samples. We measured the delta13C, delta18O and 87Sr/86Sr values of the drill core samples and REE compositions of fresh carbonate rocks, respectively. We identified two positive and two negative isotope excursions of delta13Ccarb within this interval: a moderate increase from 0 to +2 permil and a subsequent dramatic drop to -7 permil at the PC-C boundary, and a continuous increase to +5 permil at the upper part of the Nemakit-Daldynian (ND) stage and the subsequent sharp decrease to -9 permil just below the basal Tommotian unconformity, respectively. The continuous pattern of the delta13C shift is irrespective of lithotype and is comparable to fragmented records of other sections within and outside of the Yangtze Platform, indicating that the profile represents global change of seawater chemistry. A chemostratigraphy of 87Sr/86Sr ratios of the drilled samples also displays a smooth curve and its large positive anomaly just below the PC-C boundary. The estimate of oxygen content of seawater from REE composition of carbonate minerals shows significant decreases around PC-C and ND-Tommotian boundaries, respectively. The combination of chemostratigraphies of delta13C, 87Sr/86Sr and pO2 indicates that the 87Sr/86Sr excursions preceded the delta13C negative excursion at PC-C boundary, and suggests that global regression or formation of the Gondwana supercontinent, evident in increase of influx of continental materials, caused biological depression together

  16. Oceanographic and climatic evolution of the Miocene Mediterranean deduced from Nd, Sr, C, and O isotope compositions of marine fossils and sediments

    NASA Astrophysics Data System (ADS)

    Kocsis, L.; Vennemann, T. W.; Fontignie, D.; Baumgartner, C.; Montanari, A.; Jelen, B.

    2008-12-01

    Isotopic compositions of marine sediments and fossils have been investigated from northern basins of the Mediterranean to help constrain local oceanographic and climatic changes adjacent to the uplifting Alps. Stable C and O isotope compositions of benthic and planktonic foraminifera from the Umbria-Marche region (UMC) have an offset characteristic for their habitats and the changes in composition mimic global changes, suggesting that the regional conditions of climate and the carbon cycle were controlled by global changes. The radiogenic isotope composition of these fossil assemblages allows recognition of three distinct periods. In the first period, from 25 to 19 Ma, high ɛNd values and low 87Sr/86Sr of sediments and fossils support intense tectonism and volcanism, related to the opening of the western Mediterranean. In the second period, from 19 to 13 Ma the 87Sr/86Sr ratio of Mediterranean (UMC) deviate from the global ocean, which is compatible with rapid uplift of the hinterland and intense influx of Sr from Mesozoic carbonates of the western Apennines. This local control on the seawater was driven by a humid and warm climate and indicates restricted exchange of water with the global ocean. Generally, the ɛNd values of the fossils are very similar to those of Indian Ocean water, with brief periods of a decrease in the ɛNd values coinciding with volcanic events and maybe sea level variation at 15.2 Ma. In the third period, from 13 to 10 Ma the fossils have 87Sr/86Sr similar to those of Miocene seawater while their ɛNd values change considerably with time. This indicates fluctuating influence of the Atlantic versus the Paratethys and/or locally evolved seawater in the Mediterranean driven by global sea level changes. Other investigated localities near the Alps and from the ODP 900 site are compatible with this oceanographic interpretation. However, in the late early Miocene, enhanced local control, reflecting erosion of old crustal silicate rocks near the

  17. Strontium isotope characterization of wines from Quebec, Canada.

    PubMed

    Vinciguerra, Victor; Stevenson, Ross; Pedneault, Karine; Poirier, André; Hélie, Jean-François; Widory, David

    2016-11-01

    The (87)Sr/(86)Sr isotope ratios were measured on grape, wine and soil samples collected in 13 commercial vineyards located in three major wine producing areas of Quebec (Canada). The soils yield Sr isotope ratios that are intimately related to the local geology and unambiguously discriminate the different producing areas. A strong relationship exists between the (87)Sr/(86)Sr isotope ratios of the wine and the grapes. This suggests that the vinification process does not alter the overall Sr budget. Although the Sr isotope ratios of the grapes do not show a strong correlation with the bulk Sr isotope composition of the soil, they do correlate strongly with the Sr isotope composition contained in the labile fraction of the soil. This indicates that the labile fraction of the soil represents the Sr reservoir available to the plant during its growth. This study demonstrates that the Sr isotope approach can be used as a viable tool in forensic science for investigating the provenance of commercial wines.

  18. Strontium isotope characterization of wines from Quebec, Canada.

    PubMed

    Vinciguerra, Victor; Stevenson, Ross; Pedneault, Karine; Poirier, André; Hélie, Jean-François; Widory, David

    2016-11-01

    The (87)Sr/(86)Sr isotope ratios were measured on grape, wine and soil samples collected in 13 commercial vineyards located in three major wine producing areas of Quebec (Canada). The soils yield Sr isotope ratios that are intimately related to the local geology and unambiguously discriminate the different producing areas. A strong relationship exists between the (87)Sr/(86)Sr isotope ratios of the wine and the grapes. This suggests that the vinification process does not alter the overall Sr budget. Although the Sr isotope ratios of the grapes do not show a strong correlation with the bulk Sr isotope composition of the soil, they do correlate strongly with the Sr isotope composition contained in the labile fraction of the soil. This indicates that the labile fraction of the soil represents the Sr reservoir available to the plant during its growth. This study demonstrates that the Sr isotope approach can be used as a viable tool in forensic science for investigating the provenance of commercial wines. PMID:27211629

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

    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.

  20. 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.

  1. 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.

  2. Determining Effects of Diagenesis on Geochemical Dating of Plio-Pleistocene Shallow Marine Fauna

    NASA Astrophysics Data System (ADS)

    Sandstrom, R. M.; Cai, Y.; Raymo, M. E.; Goldstein, S. L.; Inglis, J. D.; Mata, R.

    2014-12-01

    Accurate dating of fossil shorelines is essential for establishing chronology related to paleo sea level changes, providing insight into past climates, paleo ice volumes and local dynamic topography. Biogenic carbonate is a particularly useful tool for dating marine terraces, as they record chemical signatures of seawater at the time of formation. However, the primary geochemical methods (marine Sr isotopes, U-series disequilibrium, and U-Pb dating) used to date shallow water fauna older than the late Pleistocene are often subject to open system effects, such as diagenesis (recrystallization and meteoric weathering). This is especially problematic for Sr isotope dating during the Mid-Pliocene, when the 87Sr/86Sr seawater calibration curve shows small changes over time, and small variations in 87Sr/86Sr ratios correspond to large uncertainties in ages. To identify pristine carbonate material that generates reliable seawater Sr isotope ratios, we examined different species of Plio-Pleistocene bivalves and corals from various geographic locations and environments by combining optical images, scanning electron microscope (SEM), cathodoluminescence and x-ray diffraction (XRD) with elemental and Sr isotope analyses of micro-drilled calcite and aragonite layers within individual organisms. The results from this study will help to evaluate the effect of secondary diagenesis and recrystallization on trace element abundances and Sr isotope ratios. Using these methods, we show that reliable ages can be achieved using the Sr isotope seawater curve.

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

    USGS Publications Warehouse

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

    2001-01-01

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

  4. Glacial recharge and paleohydrologic flow systems in the Illinois basin: Evidence from chemistry of Ordovician carbonate (Galena) formation waters

    SciTech Connect

    Stueber, A.M. ); Walter, L.M. )

    1994-11-01

    The Illinois basin provides an opportune setting for elucidating the roles of remnant evaporite brines and meteoric waters in the evolution of formation waters in an intracratonic sedimentary basin. Formation waters from carbonate reservoirs in the Upper Ordovician Galena Group have been analyzed geochemically to study the origin of their salinity, their chemical and isotopic evolution, and their relationship to paleohydrologic flow systems. Chloride/bromide ratios and Cl/Br-Na/Br relations indicate that initial brine salinity resulted from subaerial evaporation of seawater rather than from halite dissolution. Subsequent subsurface dilution of the brines by meteoric waters is disclosed by [delta]D-[delta][sup 18]O covariance; however, the remnant evaporite brine has not been completely expelled from these Ordovician strata. Galena formation waters have [sup 87]Sr/[sup 86]Sr ratios that range from 0.708 17 (a value nearly equal to that of coeval seawater) to 0.710 43. This is the greatest range of Sr isotopic ratios found in waters from any stratigraphic unit in the basin. Two fluid mixing events are revealed in plots of [sup 87]Sr/[sup 86]Sr vs. 1/Sr. 41 refs., 11 figs., 1 tab.

  5. High-precision radiogenic strontium isotope measurements of the modern and glacial ocean: Limits on glacial-interglacial variations in continental weathering

    NASA Astrophysics Data System (ADS)

    Mokadem, Fatima; Parkinson, Ian J.; Hathorne, Ed C.; Anand, Pallavi; Allen, John T.; Burton, Kevin W.

    2015-04-01

    Existing strontium radiogenic isotope (87Sr/86Sr) measurements for foraminifera over Quaternary glacial-interglacial climate cycles provide no evidence for variations in the isotope composition of seawater at the ±9-13 ppm level of precision. However, modelling suggests that even within this level of uncertainty significant (up to 30%) variations in chemical weathering of the continents are permitted, accounting for the longer-term rise in 87Sr/86Sr over the Quaternary, and the apparent imbalance of Sr in the oceans at the present-day. This study presents very high-precision 87Sr/86Sr isotope data for modern seawater from each of the major oceans, and a glacial-interglacial seawater record preserved by planktic foraminifera from Ocean Drilling Program (ODP) Site 758 in the north-east Indian ocean. Strontium isotope 87Sr/86Sr measurements for modern seawater from the Atlantic, Pacific and Indian Oceans are indistinguishable from one another (87Sr/86Sr = 0.7091792 ± 0.0000021, n = 17) at the level of precision obtained in this study (±4.9 ppm 2σ). This observation is consistent with the very long residence time of Sr in seawater, and underpins the utility of this element for high precision isotope stratigraphy. The 87Sr/86Sr seawater record preserved by planktic foraminifera shows no resolvable glacial-interglacial variation (87Sr/86Sr = 0.7091784 ± 0.0000035, n = 10), and limits the response of seawater to variations in the chemical weathering flux and/or composition to ±4.9 ppm or less. Calculations suggest that a variation of ±12% around the steady-state weathering flux can be accommodated by the uncertainties obtained here. The new data cannot accommodate a short-term weathering pulse during de-glaciation, although a more a diffuse weathering pulse accompanying protracted ice retreat is permissible. However, these results still indicate that modern weathering fluxes are potentially higher than average over the Quaternary, and such variations through

  6. Geochemical constraints on the origin of dolomite in the Ordovician Trenton and Black River limestones, Albion-Scipio area, Michigan

    SciTech Connect

    Granath, V.C. )

    1991-03-01

    The Albion-Scipio and Stoney Point oil fields in south-central Michigan produce from porous, vuggy dolomite in long linear trends associated with faulting in otherwise tight limestones. {sup 87}Sr/{sup 86}Sr ratios for undolomitized limestones (0.70796-0.70824) fall within the range for Middle Ordovician seawater given by the Burke curve and indicate they have undergone little alteration since deposition. {sup 87}Sr/{sup 86}Sr ratios for the matrix and dolomite cements in the reservoir horizons (0.70834-0.70898) are more radiogenic and overlap the range in composition for Late Silurian seawater. Thus, dolomitization might have resulted from brines dominated by Silurian seawater components. Fluid inclusion geothermometry and oxygen isotope compositions of the dolomite indicate formation under maximum burial conditions. Average freezing temperatures are {minus}29C (n = 72) and {minus}36C (n=19), respectively, indicating fluids are calcium- and magnesium-rich brines. {delta}{sup 18}O and {delta}{sup 2}H compositions of fluids in fluid inclusions are similar to data for Michigan basin brines and suggest some interaction with heavy oxygen probably from siliciclastics. These data indicate dolomitization in the Albion-Scipio area occurred under burial conditions from hot brines dominated by a Late Silurian seawater component. The brine may have been slightly modified either through mixture with another basinal fluid or interactions with siliciclastics during its circulation in the basin.

  7. High-resolution records of Bonneville Basin paleohydrology offer new insights into changing atmospheric circulation patterns over North America from 26 ka through the Holocene

    NASA Astrophysics Data System (ADS)

    Steponaitis, E.; McGee, D.; Quade, J.; Andrews, A.; Edwards, R.; Hsieh, Y.; Broecker, W. S.; Cheng, H.

    2013-12-01

    The tremendous lateral extent of the Bonneville Basin, which covers much of western Utah, makes paleoclimate records from this region highly sensitive to global-scale changes in atmospheric circulation and hydrology. New paleoclimate records from speleothems and lacustrine carbonates offer insight into the hydrology the Bonneville Basin spanning from 26 ka through the Holocene. Anchored by high-precision U-Th dates, Sr records from crystalline lacustrine carbonates from throughout the basin provide a mechanism for constraining zonal variations in precipitation over time. To accomplish this, we exploit spatial variations in the 87Sr/86Sr ratios of fluvial inputs to Lake Bonneville (Hart et al. 2004). Paired with stable isotope records, these Sr records give a spatially detailed view of the response of Great Basin to global climate change, and by extension, insight into atmospheric circulation patterns over North America during abrupt climate changes. Stable isotope and trace metal records from Lehman Cave speleothems provide a high-resolution extension of these Great Basin hydrological records into the Holocene. Here we provide an overview of these unique paired records, focusing particular attention on the region's response to the Younger Dryas and Heinrich events 1 and 2. Hart, W.S. et al., The 87Sr/86Sr ratios of lacustrine carbonates and lake-level history of the Bonneville paleolake system. GSA Bulletin. 2004; 116: 1107-1119.

  8. 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.

  9. Geochemistry of core samples of the Tiva Canyon Tuff from drill hole UE-25 NRG{number_sign}3, Yucca Mountain, Nevada

    SciTech Connect

    Peterman, Z.E.; Futa, K.

    1996-07-01

    The Tiva Canyon Tuff of Miocene age is composed of crystal-poor, high-silica rhyolite overlain by a crystal-rich zone that is gradational in composition from high-silica rhyolite to quartz latite. Each of these zones is divided into subzones that have distinctive physical, mineralogical, and geochemical features.Accurate identification of these subzones and their contacts is essential for detailed mapping and correlation both at the surface and in the subsurface in drill holes and in the exploratory studies facility (ESF). This report presents analyses of potassium (K), calcium (Ca), titanium (Ti), rubidium (Rb), strontium (Sr), yttrium (Y), zirconium (Zr), niobium (Nb), barium (Ba), lanthanum (La), and cerium (Ce) in core samples of the Tiva Canyon Tuff from drill hole UE-25 NRG {number_sign}3. The concentrations of most of these elements are remarkably constant throughout the high-silica rhyolite, but at its upper contact with the crystal-rich zone, Ti, Zr, Ba, Ca, Sr, La, Ce, and K begin to increase progressively through the crystal-rich zone. In contrast, Rb and Nb decrease, and Y remains essentially constant. Initial {sup 87}Sr/{sup 86}Sr ratios are relatively uniform in the high-silica rhyolite with a mean value of 0.7117, whereas initial {sup 87}Sr/{sup 86}Sr ratios decrease upward in the quartz latite to values as low as 0.7090.

  10. Multiple episodes of dolomitization in the Arbuckle Group, Arbuckle Mountains, south-central Oklahoma: Field, petrographic, and geochemical evidence

    SciTech Connect

    Gao, G.; Land, L.S.; Elmore, R.D.

    1995-04-03

    The Cambro-Ordovician Arbuckle Group in the Arbuckle Mountains, south-central Oklahoma, had a complex history of dolomitization that resulted in two different geometries of dolomite bodies: stratal dolomite, of stratigraphically consistent, widespread distribution, and non-stratal dolomite, of stratigraphically inconsistent, local occurrence. Stratal dolomite includes the Royer and Butterly units in the lower Arbuckle Group. Most stratal dolomite samples are coarsely crystalline and have {sup 87}Sr/{sup 86}Sr ratios similar to Late Cambrian limestone and coeval seawater. All stratal dolomite and Arbuckle limestone samples have low {Delta}{sup 18}O values. Nonstratal dolomite is present in two areas: the Tishomingo Anticline and the Arbuckle Anticline. In the Tishomingo Anticline area, massive bodies (> 10 km{sup 2}) of nonstratal dolomite are present in a paleokarst system of pre-Middle Ordovician age. The petrographic and isotopic characteristics suggest that the nonstratal dolomite probably resulted from dolomitization of recrystallized limestone by post-Early Ordovician seawater. In the Arbuckle Anticline area, nonstratal dolomite is present as small irregular bodies that are related to Pennsylvanian faults and are associated with the margins of stratal Butterly dolomite. The nonstratal dolomite, medium to coarsely crystalline and brightly luminescent, is characterized by high {sup 87}Sr/{sup 86}Sr ratios values, and Fe and Mn concentrations, relative to all Arbuckle carbonates. Such compositions suggest that this type of dolomite probably originated from fluids that were derived from the adjacent basin(s) during late Paleozoic time.

  11. Constraints on water chemistry by chemical weathering in the Lake Qinghai catchment, northeastern Tibetan Plateau (China): clues from Sr and its isotopic geochemistry

    NASA Astrophysics Data System (ADS)

    Jin, Zhangdong; Yu, Jimin; Wang, Sumin; Zhang, Fei; Shi, Yuewei; You, Chen-Feng

    2009-12-01

    Lake water, river water, and groundwater from the Lake Qinghai catchment in the northeastern Tibetan Plateau, China have been analyzed and the results demonstrate that the chemical components and 87Sr/86Sr ratios of the waters are strictly constrained by the age and rock types of the tributaries, especially for groundwater. Dissolved ions in the Lake Qinghai catchment are derived from carbonate weathering and part from silicate sources. The chemistry of Buha River water, the largest tributary within the catchment, underlain by the late Paleozoic marine limestone and sandstones, constrains carbonate-dominated compositions of the lake water, being buffered by the waters from the other tributaries and probably by groundwater. The variation of 87Sr/86Sr ratios with cation concentrations places constraint on the Sr-isotopic compositions of the main subcatchments surrounding Lake Qinghai. The relative significance of river-water sources from different tributaries (possibly groundwater as well) in controlling the Sr distribution in Lake Qinghai provides the potential to link the influence of hydrological processes to past biological and physical parameters in the lake. The potential role of groundwater input in the water budget and chemistry of the lake emphasizes the need to further understand hydrogeological processes within the Lake Qinghai system.

  12. Movements of Diadromous Fish in Large Unregulated Tropical Rivers Inferred from Geochemical Tracers

    PubMed Central

    Walther, Benjamin D.; Dempster, Tim; Letnic, Mike; McCulloch, Malcolm T.

    2011-01-01

    Patterns of migration and habitat use in diadromous fishes can be highly variable among individuals. Most investigations into diadromous movement patterns have been restricted to populations in regulated rivers, and little information exists for those in unregulated catchments. We quantified movements of migratory barramundi Lates calcarifer (Bloch) in two large unregulated rivers in northern Australia using both elemental (Sr/Ba) and isotope (87Sr/86Sr) ratios in aragonitic ear stones, or otoliths. Chemical life history profiles indicated significant individual variation in habitat use, particularly among chemically distinct freshwater habitats within a catchment. A global zoning algorithm was used to quantify distinct changes in chemical signatures across profiles. This algorithm identified between 2 and 6 distinct chemical habitats in individual profiles, indicating variable movement among habitats. Profiles of 87Sr/86Sr ratios were notably distinct among individuals, with highly radiogenic values recorded in some otoliths. This variation suggested that fish made full use of habitats across the entire catchment basin. Our results show that unrestricted movement among freshwater habitats is an important component of diadromous life histories for populations in unregulated systems. PMID:21494693

  13. Geochemistry of late Cretaceous granitoids from northeastern Washington: implication for genesis of two-mica Cordilleran granites

    SciTech Connect

    Asmerom, Y.; Ikramuddin, M.; Kinart, K.

    1988-05-01

    Mesozoic two-mica granites and I-type granodiorites from northeastern Washington have initial /sup 87/Sr//sup 86/Sr ratios around 0.7100, similar to many other Cordilleran granitoids. Metapelite and calcsilicate country rocks, equivalent to the Belt Supergroup, have measured /sup 87/Sr//sup 86/Sr ratios in the range of 0.91 to 0.98. Unlike many of their Cordilleran counterparts, the northeastern Washington two-mica granites are enriched in U, Rb, and other incompatible elements, and therefore cannot have been derived from depleted lower crust sedimentary sources. Both the two-mica granites and the I-type granodiorites have similar rare-earth-element and trace-element enrichment patterns. Trace-elements modeling shows that it is feasible to derive the two-mica granites by 60% partial melting of a granodiorite-like source. The close association of Cordilleran metamorphic core complexes and older I-type granodiorites with two-mica granites supports this model.

  14. Strontium isotope record of seasonal scale variations in sediment sources and accumulation in low-energy, subtidal areas of the lower Hudson River estuary

    USGS Publications Warehouse

    Smith, J.P.; Bullen, T.D.; Brabander, D.J.; Olsen, C.R.

    2009-01-01

    Strontium isotope (87Sr/86Sr) profiles in sediment cores collected from two subtidal harbor slips in the lower Hudson River estuary in October 2001 exhibit regular patterns of variability with depth. Using additional evidence from sediment Ca/Sr ratios, 137Cs activity and Al, carbonate (CaCO3), and organic carbon (OCsed) concentration profiles, it can be shown that the observed variability reflects differences in the relative input and trapping of fine-grained sediment from seaward sources vs. landward sources linked to seasonal-scale changes in freshwater flow. During high flow conditions, the geochemical data indicate that most of the fine-grained sediments trapped in the estuary are newly eroded basin materials. During lower (base) flow conditions, a higher fraction of mature materials from seaward sources with higher carbonate content is trapped in the lower estuary. Results show that high-resolution, multi-geochemical tracer approaches utilizing strontium isotope ratios (87Sr/86Sr) can distinguish sediment sources and constrain seasonal scale variations in sediment trapping and accumulation in dynamic estuarine environments. Low-energy, subtidal areas such as those in this study are important sinks for metastable, short-to-medium time scale sediment accumulation. These results also show that these same areas can serve as natural recorders of physical, chemical, and biological processes that affect particle and particle-associated material dynamics over seasonal-to-yearly time scales. ?? 2009.

  15. Linking soil, water, and honey composition to assess the geographical origin of argentinean honey by multielemental and isotopic analyses.

    PubMed

    Baroni, María V; Podio, Natalia S; Badini, Raúl G; Inga, Marcela; Ostera, Héctor A; Cagnoni, Mariana; Gautier, Eduardo A; García, Pilar Peral; Hoogewerff, Jurian; Wunderlin, Daniel A

    2015-05-13

    The objective of this research was to investigate the development of a reliable fingerprint from elemental and isotopic signatures of Argentinean honey to assess its geographical provenance. Honey, soil, and water from three regions (Córdoba, Buenos Aires, and Entre Rı́os) were collected. The multielemental composition was determined by ICP-MS. δ(13)C was measured by isotopic ratio mass spectrometry, whereas the (87)Sr/(86)Sr ratio was determined using thermal ionization mass spectrometry. The data were analyzed by chemometrics looking for the association between the elements, stable isotopes, and honey samples from the three studied areas. Honey samples were differentiated by classification trees and discriminant analysis using a combination of eight key variables (Rb, K/Rb, B, U, (87)Sr/(86)Sr, Na, La, and Zn) presenting differences among the studied regions. The application of canonical correlation analysis and generalized procrustes analysis showed 91.5% consensus between soil, water, and honey samples, in addition to clear differences between studied areas. To the authors' knowledge, this is the first report demonstrating the correspondence between soil, water, and honey samples using different statistical methods, showing that elemental and isotopic honey compositions are related to soil and water characteristics of the site of origin.

  16. Movements of diadromous fish in large unregulated tropical rivers inferred from geochemical tracers.

    PubMed

    Walther, Benjamin D; Dempster, Tim; Letnic, Mike; McCulloch, Malcolm T

    2011-04-06

    Patterns of migration and habitat use in diadromous fishes can be highly variable among individuals. Most investigations into diadromous movement patterns have been restricted to populations in regulated rivers, and little information exists for those in unregulated catchments. We quantified movements of migratory barramundi Lates calcarifer (Bloch) in two large unregulated rivers in northern Australia using both elemental (Sr/Ba) and isotope ((87)Sr/(86)Sr) ratios in aragonitic ear stones, or otoliths. Chemical life history profiles indicated significant individual variation in habitat use, particularly among chemically distinct freshwater habitats within a catchment. A global zoning algorithm was used to quantify distinct changes in chemical signatures across profiles. This algorithm identified between 2 and 6 distinct chemical habitats in individual profiles, indicating variable movement among habitats. Profiles of (87)Sr/(86)Sr ratios were notably distinct among individuals, with highly radiogenic values recorded in some otoliths. This variation suggested that fish made full use of habitats across the entire catchment basin. Our results show that unrestricted movement among freshwater habitats is an important component of diadromous life histories for populations in unregulated systems.

  17. Hydrogeochemical and isotopic investigations of the Han River basin, South Korea

    NASA Astrophysics Data System (ADS)

    Ryu, Jong-Sik; Lee, Kwang-Sik; Chang, Ho-Wan

    2007-10-01

    SummaryThe Han River, the largest river in South Korea draining approximately 26,000 km 2, comprises two major tributaries: the North and the South Han Rivers. Seasonal and spatial variations in the major ion chemistry and isotope compositions of the Han River were monitored for one year at 14-23 locations, covering about 80% of the entire drainage basin. Compared to the South Han River (SHR), the North Han River (NHR) was much lower in total dissolved solids (TDS), Sr, and major ion concentrations, but higher in Si concentration, δ 34S SO 4 values, and 87Sr/ 86Sr ratios. These observations suggest strong influence of prevailing rock types in the drainage basins on the chemical and isotopic compositions of the river waters. These are silicate rocks in the NHR basin and carbonate rocks in the SHR basin. The headwaters of the NHR basin, where several flood control dams have been constructed, show enrichment in deuterium and oxygen-18, indicating evaporative loss. The δ 34S SO 4 data suggest dissolved sulfates in the NHR and SHR are mostly derived from atmospheric deposition, and variable mixtures of atmospheric deposition and sulfide oxidation, respectively. The 87Sr/ 86Sr ratios are much higher in the NHR (0.71793-0.72722) than in the SHR (0.71495-0.71785) with one exception, indicating weathering of Precambrian and Mesozoic granitic rocks and marine carbonates, respectively.

  18. Geochemical constraints on the origin of secondary magnetizations in the Cambro-Ordovician Royer Dolomite, Arbuckle Mountains, southern Oklahoma

    NASA Astrophysics Data System (ADS)

    Elmore, R. D.; Cates, K.; Gao, G.; Land, L.

    1994-08-01

    Geochemical and paleomagnetic results from Cambro-Ordovician Royer Dolomite in the Arbuckle Mountains, southern Oklahoma, suggest a connection between dolomite type and magnetizations. One dolomite type, which is most common in the vicinity of the Arbuckle Anticline, has a dull luminescence, low δ18O values, coeval to slightly lower 87Sr/86Sr ratios and contains an easterly Cambro-Ordovician magnetization in magnetite. To the southeast, closer to the Ouachita Mountain front, most of the Royer dolomite contains a southeasterly and shallow magnetization in magnetite that is interpreted to be Late Paleozoic in age. In contrast to the other dolomites, these dolomites contain abundant authigenic K-feldspar and pyrite, radiogenic 87Sr/86Sr ratios, and have a bright (red) luminescence, all of which are consistent with alteration by basinal fluids. At one site, a stromatolitic bioherm, dolomites similar to those at the Arbuckle Anticline are surrounded by the altered dolomites. The distribution of specimen directions at this site is streaked between a Cambro-Ordovician and Late Paleozoic direction. The results of this study suggest a connection, either direct (by causing precipitation) or indirect (by increasing permeabilities for another fluid), between a radiogenic fluid and a chemical magnetization in magnetite. The relatively unaltered dolomites at the stromatolitic bioherm site escaped the almost pervasive alteration and remagnetization caused by the basinal fluids close to the Ouachita Mountains, a potential source for the fluids.

  19. The application of Mg isotopes in carbonate rocks to reconstruct environmental records

    NASA Astrophysics Data System (ADS)

    Wang, Z.; Liu, C.

    2014-12-01

    Previous studies showed that Mg isotope fractionation between carbonate and solution depends on several parameters including 1) temperature (with a sensitivity of ~0.01‰/oC); 2) precipitation rate; 3) aqueous Mg concentration and pH; 4) mineralogy: All else being equal, the enrichment of 26Mg in carbonate precipitated from solutions with the same δ26Mg values follow the sequence: aragonite > dolomite > magnesite > calcite; and 5) biogenic effect [1]. Despite the complexity, the weak temperature sensitivity and strong mineralogical control offer Mg isotope compositions of carbonate rocks as a paleoproxy to provide constraints on environmental records, and an index for diagenesis and low degree metamorphism. Here, we present four cases describing 1) how Mg isotope varied during the mineralogical transition from aragonite (corals) to calcite; 2) how δ26Mg, 87Sr/86Sr ratios of a Cambrian limestone changed due to the formation of secondary high-Mg calcite; 3) how δ26Mg and trace metal compositions of limestones can be used to reconstruct ocean chemistry, and 4) how δ26Mg, 87Sr/86Sr ratios of dolomite can be used to infer ocean chemistry in the deep time.

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

    SciTech Connect

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

    2001-08-01

    The chemical and isotopic ({sup 11}B/{sup 10}B, {sup 87}Sr/{sup 86}Sr, {sup 18}O/{sup 16}O, {sup 2}H/H, {sup 13}C/{sup 12}C, {sup 14}C, {sup 3}He/{sup 3}H) compositions of groundwater from the upper aquifer system of the Salinas Valley in coastal central California were investigated in order to delineate the origin and processes of groundwater contamination in this complex system. The Salinas Valley has a relatively deep, confined ''400-foot'' aquifer, overlain by a ''180-foot'' aquifer, and a shallower perched aquifer, all made up of alluvial sand, gravel, and clay deposits. Groundwater from the aquifers have different {sup 14}C ages; fossil ({sup 14}C = 21.3 pmc) for the 400-foot, and modern ({sup 14}C = 72.2 to 98.2 pmc) for the 180-foot. Fresh groundwater in all aquifers is recharged naturally and artificially and through the Salinas River. The two modes of recharge can be distinguished chemically. We identified several different saline components with distinguishable chemical and isotopic fingerprints. (1) Salt-water intrusion in the northern basin has Cl concentrations up to 1700 mg/l, a Na/Cl ratio ratio, a Ca/Cl ratio >seawater, {delta}{sup 11}B between +17 and +38 per mil, and {sup 87}Sr/{sup 86}Sr between 0.7088 and 0.7096. Excess dissolved Ca, relative to the expected concentration for simple dilution of seawater, correlates with {sup 87}Sr/{sup 86}Sr ratios, suggesting base exchange reaction with clay minerals. (2) Agriculture return flow is high in NO{sub 3} and SO{sub 4}, with a {sup 87}Sr/{sup 86}Sr = 0.7082, {delta}{sup 11}B = 19 per mil; and {delta}{sup 13}C between -23 and -17 per mil. The {sup 3}H-{sup 3}He ages (5-17 years) and {sup 14}C data suggest vertical infiltration rates of irrigation water of 3 to 10 m/yr. (3) Non-marine saline water in the southern part of the valley has high TDS up to 3800 mg/l, high SO{sub 4}, Na/Cl ratio >1, {delta}{sup 11}B between +24 and +30 per mil, and {sup 87}Sr/{sup 86}Sr = 0

  1. Isotopic microanalysis sheds light on the magmatic endmembers feeding volcanic eruptions: The Astroni 6 case study (Campi Flegrei, Italy)

    NASA Astrophysics Data System (ADS)

    Arienzo, I.; D'Antonio, M.; Di Renzo, V.; Tonarini, S.; Minolfi, G.; Orsi, G.; Carandente, A.; Belviso, P.; Civetta, L.

    2015-10-01

    Sr-isotopic microanalysis has been performed on selected minerals from the Campi Flegrei caldera, together with Sr and Nd isotopic ratio determinations on bulk mineral and glass fractions. The aim was a better characterization of the chemically homogeneous, but isotopically distinct magmatic components which fed volcanic eruptions of the caldera over the past 5 ka, in order to enhance our knowledge about one of the most dangerous volcanoes on Earth. Information on the involved magmatic endmembers, unobtainable by analyzing the isotopic composition of whole rock samples and bulk mineral fractions, has been acquired through high-precision determination of 87Sr/86Sr on single crystals and microdrilled mineral powders. We focused our investigations on the products emplaced during the Astroni 6 eruption (4.23 cal ka BP), assumed representative of the expected event in case of renewed volcanic activity in the Campi Flegrei caldera. Data on single crystals and microdrilled mineral powders have been compared with Sr and Nd isotopic compositions of bulk mineral fractions from products emplaced during the whole Astroni activity, which included seven distinct eruptions. The 87Sr/86Sr ratios of single crystals and microdrilled mineral powders are in the 0.7060 to 0.7076 range, much wider than that of bulk mineral fractions, which range from 0.7066 to 0.7076. Moreover, the Sr isotopic ratios are inversely correlated to 143Nd/144Nd. The new data allow us to better define the magmatic endmembers involved in mingling/mixing processes that occurred prior to/during the Astroni activity. One magmatic endmember, characterized by average 87Sr/86Sr ratio of ~ 0.70750, was quite common in the past 15 ka activity of the Campi Flegrei caldera; the other, as evidenced by the isotopic composition of single feldspar and clinopyroxene crystals, is less enriched in radiogenic Sr (87Sr/86Sr ~ 0.70724). The latter is interpreted to represent a new magmatic component that entered the Campi Flegrei

  2. Magma Genesis of Sakurajima, the Quaternary post- Aira caldera volcano, southern Kyushu Island, Japan

    NASA Astrophysics Data System (ADS)

    Shibata, T.; Suzuki, J.; Yoshikawa, M.; Kobayashi, T.; Miki, D.; Takemura, K.

    2012-12-01

    from the mixing curve to the direction of being more radiogenic when we observe in more detail. This observation supports our conclusion that the crustal materials contribute the magma genesis of Sakurajima volcano emphasized from Zr/Nb ratios. Low-P and high-P groups show different trends of SiO2, P2O5, TiO2 concentrations and 87Sr/86Sr ratios relative to plagioclase modal abundances. The high-P group samples show continuous trends, and their 87Sr/86Sr ratios increase with decreasing plagioclase, representing simple AFC process. The SiO2 content of low-P group rapidly increases from 63 to 66 wt. % at the modal abundance of pl is nearly 20 vol. %. The Sr isotope ratios of low-P group with < 20 vol. % of pl are obviously high (87Sr/86Sr = 0.70556 to 0.70569) compared to those of high-P group (87Sr/86Sr = 0.705136 to 0.705285). From these observations, we conclude that the rapid increase of SiO2 with high 87Sr/87Sr ratio infer involvement of crustal materials to the magma chamber, in which the ACF process is proceeding.

  3. Biochronostratigraphy and paleoenvironment analysis of Neogene deposits from the Pelotas Basin (well 2-TG-96-RS), Southernmost Brazil.

    PubMed

    Silva, Wagner G; Zerfass, Geise S A; Souza, Paulo A; Helenes, Javier

    2015-09-01

    This paper presents the integration of micropaleontological (palynology and foraminifera) and isotopic (87Sr/86Sr) analysis of a selected interval from the well 2-TG-96-RS, drilled on the onshore portion of the Pelotas Basin, Rio Grande do Sul, Brazil. A total of eight samples of the section between 140.20 and 73.50 m in depth was selected for palynological analysis, revealing diversified and abundant palynomorph associations. Species of spores, pollen grains and dinoflagellate cysts are the most common palynomorphs found. Planktic and benthic calcareous foraminifera were recovered from the lowest two levels of the section (140.20 and 134.30 m). Based on the stratigraphic range of the species of dinoflagellate cysts and sporomorphs, a span age from Late Miocene to Early Pliocene is assigned. The relative age obtained from the 87Sr/86Sr ratio in shells of calcareous foraminifers indicates a Late Miocene (Messinian) correspondence, corroborating the biostratigraphic positioning performed with palynomorphs. Paleoenvironmental interpretations based on the quantitative distribution of organic components (palynomorphs, phytoclasts and amorphous organic matter) throughout the section and on foraminiferal associations indicate a shallow marine depositional environment for the section. Two palynologicals intervals were recognized based on palynofacies analysis, related to middle to outer shelf (140.20 to 128.90 m) and inner shelf (115.75 to 73.50 m) conditions.

  4. Geochemistry and geochronology of late Mesozoic volcanic rocks in the northern part of the Eastern Pontide Orogenic Belt (NE Turkey): Implications for the closure of the Neo-Tethys Ocean

    NASA Astrophysics Data System (ADS)

    Özdamar, Şenel

    2016-04-01

    This paper presents 40Ar/39Ar and U-Pb age data, Sr-Nd isotopes, whole-rock and mineral compositions of Upper Cretaceous volcanic rocks from the Ordu area of the Eastern Pontide Orogenic Belt (EPOB) in northeastern Turkey. The volcanic rocks exhibit a wide compositional range: basalt, basaltic-andesites, andesites and a rhyodacite suite; they are characterized by subparallel light rare earth element (LREE)-enrichment, relatively flat heavy rare earth element (HREE) patterns with Eu anomalies and moderate fractionation [average (La/Yb)N = 8.55]. The geochemical results show that the volcanic rocks have calc-alkaline affinity consistent with arc volcanic rocks erupted in an active continental margin. Initial 87Sr/86Sr values vary between 0.70569 and 0.70606, while initial 143Nd/144Nd values lie between 0.51244 and 0.51249. Crustal contamination affected the mantle-originated primary magma, as indicated by increased 87Sr/86Sr and decreased 143Nd/144Nd ratios with increasing SiO2. New precise laser ablation inductively coupled plasma mass spectrometer (LA-ICP-MS) 206Pb-238U age analyses of zircon and 40Ar/39Ar age data of plagioclase from the volcanics enable a more precise reconstruction of the EBOP. The ages provide insight into the timing of arc formation in this region, constrain the volcanic activity between 86 My (Coniacian) and 75 My (Campanian) and constrain the timing of closure of the Neo-Tethys.

  5. Dissected hydrologic system at the Grand Canyon: Interaction between deeply derived fluids and plateau aquifer waters in modern springs and travertine

    NASA Astrophysics Data System (ADS)

    Crossey, Laura J.; Fischer, Tobias P.; Patchett, P. Jonathan; Karlstrom, Karl E.; Hilton, David R.; Newell, Dennis L.; Huntoon, Peter; Reynolds, Amanda C.; de Leeuw, Goverdina A. M.

    2006-01-01

    Geochemical study of water and gas discharging from the deeply incised aquifer system at the Grand Canyon, Arizona, provides a paradigm for understanding complex groundwater mixing phenomena, and Quaternary travertines deposited from cool springs provide a paleohydrologic record of this mixing. Geochemical data show that springs have marked compositional variability: those associated with active travertine accumulations (deeply derived endogenic waters) are more saline, richer in CO2, and elevated in 87Sr/86Sr relative to springs derived dominantly from surface recharge of plateau aquifers (epigenic waters). Endogenic waters and associated travertine are preferentially located along basement-penetrating faults. We propose a model whereby deeply derived fluids are conveyed upward via both magmatism and seismicity. Our model is supported by: (1) gas analyses from spring waters with high He/Ar and He/N2 and 3He/4He ratios indicating the presence of mantle-derived He; (2) large volumes of travertine and CO2-rich gases in springs recording high CO2 fluxes; and (3) 87Sr/86Sr in these springs that indicate circulation of waters through Precambrian basement. Geochemical trends are explained by mixing of epigenic waters of the Colorado Plateau aquifers with different endogenic end-member waters in different tectonic subprovinces. Endogenic waters are volumetrically minor but have significant effects on water chemistry. They are an important and largely unrecognized component of the hydrogeochemistry and neotectonics of the southwestern United States.

  6. Fish remains from Homestead Cave and lake levels of the past 13,000 years in the Bonneville basin

    USGS Publications Warehouse

    Broughton, J.M.; Madsen, D.B.; Quade, Jay

    2000-01-01

    A late Quaternary ichthyofauna from Homestead Cave, Utah, provides a new source of information on lake history in the Bonneville basin. The fish, represented by 11 freshwater species, were accumulated between ~11,200 and ~1000 14C yr B.P. by scavenging owls. The 87Sr/86Sr ratio of Lake Bonneville varied with its elevation; 87Sr/86Sr values of fish from the lowest stratum of the cave suggest they grew in a lake near the terminal Pleistocene Gilbert shoreline. In the lowest deposits, a decrease in fish size and an increase in species tolerant of higher salinities or temperatures suggest multiple die-offs associated with declining lake levels. An initial, catastrophic, post-Provo die-off occurred at 11,300-11,200 14C yr B.P. and was followed by at least one rebound or recolonization of fish populations, but fish were gone from Lake Bonneville sometime before ~10,400 14C yr B.P. This evidence is inconsistent with previous inferences of a near desiccation of Lake Bonneville between 13,000 and 12,000 14C yr B.P. Peaks in Gila atraria frequencies in the upper strata suggest the Great Salt Lake had highstands at ~3400 and ~1000 14C yr B.P. (C) 2000 University of Washington.

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

    NASA Astrophysics Data System (ADS)

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

    2002-08-01

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

  8. Biochronostratigraphy and paleoenvironment analysis of Neogene deposits from the Pelotas Basin (well 2-TG-96-RS), Southernmost Brazil.

    PubMed

    Silva, Wagner G; Zerfass, Geise S A; Souza, Paulo A; Helenes, Javier

    2015-09-01

    This paper presents the integration of micropaleontological (palynology and foraminifera) and isotopic (87Sr/86Sr) analysis of a selected interval from the well 2-TG-96-RS, drilled on the onshore portion of the Pelotas Basin, Rio Grande do Sul, Brazil. A total of eight samples of the section between 140.20 and 73.50 m in depth was selected for palynological analysis, revealing diversified and abundant palynomorph associations. Species of spores, pollen grains and dinoflagellate cysts are the most common palynomorphs found. Planktic and benthic calcareous foraminifera were recovered from the lowest two levels of the section (140.20 and 134.30 m). Based on the stratigraphic range of the species of dinoflagellate cysts and sporomorphs, a span age from Late Miocene to Early Pliocene is assigned. The relative age obtained from the 87Sr/86Sr ratio in shells of calcareous foraminifers indicates a Late Miocene (Messinian) correspondence, corroborating the biostratigraphic positioning performed with palynomorphs. Paleoenvironmental interpretations based on the quantitative distribution of organic components (palynomorphs, phytoclasts and amorphous organic matter) throughout the section and on foraminiferal associations indicate a shallow marine depositional environment for the section. Two palynologicals intervals were recognized based on palynofacies analysis, related to middle to outer shelf (140.20 to 128.90 m) and inner shelf (115.75 to 73.50 m) conditions. PMID:26312424

  9. Petrogenesis of tholeiitic basalts from the Central Atlantic magmatic province as revealed by mineral major and trace elements and Sr isotopes

    NASA Astrophysics Data System (ADS)

    Marzoli, Andrea; Jourdan, Fred; Bussy, François; Chiaradia, Massimo; Costa, Fidel

    2014-02-01

    The petrogenesis of the Kerforne dyke tholeiitic basalts (Brittany, France), the northernmost outcrop of the 200 Ma Central Atlantic magmatic province (CAMP), is constrained by its zoned augite and plagioclase crystals. Augite cores with high Mg/Fe and Cr suggest crystallization from near-primary magmas, with slightly enriched Rare Earth element (REE) patterns. Plagioclase crystals with high-An (An85) rounded cores are MgO- and K-rich, REE-poor, and display 87Sr/86Sr200Ma (0.7058) significantly higher than those of the surrounding ground-mass (0.7052-0.7053) suggesting open-system evolution processes. We propose a differentiation process involving mixing of different mafic magmas which occurred in less than a few hundred years judging from the lack of diffusive re-equilibration of major and trace elements in augite and of 87Sr/86Sr200Ma in plagioclase cores. The relatively large range of incompatible element contents and ratios of observed and calculated magmas are possibly due to fractional crystallization and to moderate amounts of crustal contamination which affected the more primitive magmas in particular. The calculated magmas reach near-primitive compositions and suggest that they originated from melting of a spinel peridotite slightly enriched in LREE vs. HREE.

  10. A Nd, Sr and O isotopic investigation into the causes of chemical and isotopic zonation in the Bishop Tuff, California

    USGS Publications Warehouse

    Halliday, A.N.; Fallick, A.E.; Hutchinson, J.; Hildreth, W.

    1984-01-01

    The Bishop Tuff represents a single eruption of chemically zoned rhyolitic magma. Six whole rock samples spanning the compositional and temperature range yield initial 87Sr 86Sr of 0.7060-0.7092 and ??18O of 5.9-10.3???. Six constituent sanidines yield smaller ranges of initial 87Sr 86Sr of 0.7061-0.7069 and ??18O of 6.7-7.9. In contrast 143Nd 144Nd ratios for the six whole rocks and two constituent magnetites exhibit negligible variation with a mean of 0.51258 ?? 1. These data are used to show that the phenocrysts were precipitated from an already chemically zoned liquid, that the zoning process involved negligible assimilation of, or exchange with, country rocks and that the extreme Sr and O isotopic disequilibria are probably the result of post-eruptive interaction with meteoric water. The parent magma had ??Nd = -0.9, ??Sr = +23 and ??18O = 7??? and was formed from mantle-derived magmas and/or melts of lower crustal rocks isotopically similar to parts of the Sierra Nevada Batholith. ?? 1984.

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

    USGS Publications Warehouse

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

    1984-01-01

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

  12. Who provided maize to Chaco Canyon after the mid-12th-century drought?

    USGS Publications Warehouse

    Benson, L.V.

    2010-01-01

    Between A.D. 1181 and 1200, in the early part of a climatically wet period, corn was imported to Chaco Canyon from a region outside the Chaco Halo (defined in this paper as the region between the base of the Chuska Mountains and Raton Wells). Strontium-isotope (87Sr/86Sr) analyses of 12 corn cobs dating to this period match 87Sr/86Sr ratios from five potential source areas, including: the Zuni region, the Mesa Verde-McElmo Dome area, the Totah, the Defiance Plateau, and Lobo Mesa. The latter two areas were eliminated from consideration as possible sources of corn in that they appear to have been unpopulated during the time period of interest. Therefore, it appears that the corn cobs were imported from the Zuni region, the Mesa Verde-McElmo Dome area, or the Totah area during a time when the climate was relatively wet and when a surplus of corn was produced in regions outside Chaco Canyon. Based on proximity to and cultural affiliation with Chaco Canyon, it is hypothesized that the corn probably was imported from the Totah.

  13. Isotopic and geochemical characterization of fossil brines of the Cambrian Mt. Simon Sandstone and Ironton-Galesville Formation from the Illinois Basin, USA

    NASA Astrophysics Data System (ADS)

    Labotka, Dana M.; Panno, Samuel V.; Locke, Randall A.; Freiburg, Jared T.

    2015-09-01

    Geochemical and isotopic characteristics of deep-seated saline groundwater provide valuable insight into the origin and evolving composition, water-rock interaction, and mixing potential of fossil brines. Such information may yield insight into intra- and interbasinal brine movement and relationships between brine evolution and regional groundwater flow systems. This investigation reports on the δ18O and δD composition and activity values, 87Sr/86Sr ratios and Sr concentrations, and major ion concentrations of the Cambrian-hosted brines of the Mt. Simon Sandstone and Ironton-Galesville Formation and discusses the evolution of these brines as they relate to other intracontinental brines. Brines in the Illinois Basin are dominated by Na-Ca-Cl-type chemistry. The Mt. Simon and overlying Ironton-Galesville brines exhibit total dissolved solids concentrations of ∼195,000 mg/L and ∼66,270 mg/L, respectively. The δD of brine composition of the Mt. Simon ranges from -34‰ to -22‰ (V-SMOW), and the Ironton-Galesville is ∼-53.2‰ (V-SMOW). The δ18O composition of the Mt. Simon brine ranges from -5.0‰ to -2.8‰ (V-SMOW), and the Ironton-Galesville brine is ∼-6.9‰ (V-SMOW). The 87Sr/86Sr values in the Mt. Simon brine range from 0.7110 to 0.7116. The less radiogenic Ironton-Galesville brine has an average 87Sr/86Sr value of 0.7107. Evaluation of δ18O and δD composition and activities and 87Sr/86Sr ratios suggests that the Mt. Simon brine is likely connate seawater and recirculating deep-seated brines that have been diluted with meteoric water and influenced by the dissolution of evaporites with a minimal halite contribution based on Cl/Br ratios. The Ironton-Galesville brine is also likely originally connate seawater that mixed with other brines and meteoric waters, including possibly Pleistocene glacial recharge. The Ca-excess vs. Na-deficiency comparison with the Basinal Fluid Line suggests the Mt. Simon and Ironton-Galesville brines have been

  14. Mineralogical and strontium isotopic record of hydrothermal processes in the lower ocean crust at and near the East Pacific Rise

    NASA Astrophysics Data System (ADS)

    Kirchner, Timo M.; Gillis, Kathryn M.

    2012-07-01

    Tectonic exposures of upper plutonics (>800 m) that are part of a contiguous section of young East Pacific Rise (EPR) crust at the Hess Deep Rift provide the first regional-scale constraints on hydrothermal processes in the upper plutonic crust formed at a fast-spreading ridge. Submersible-collected samples recovered over a 4-km-wide region show that the sheeted dike complex is largely underlain by a 150- to 200-m-thick gabbro unit, followed by a more primitive gabbronorite unit. Gabbroic samples are variably altered by pervasive fluid flow along fracture networks to amphibole-dominated assemblages. The gabbroic rocks are significantly less altered (average 11% hydrous phases) than the overlying sheeted dike complex (average 24%), and the percentage of hydrous alteration diminishes with depth. Incipient, pervasive fluid flow occurred at amphibolite facies conditions (average 720°C), with slightly higher temperatures in the lower 500 m of the section. The extent of subsequent lower-temperature alteration is generally low and regionally variable. The gabbroic samples are slightly elevated in 87Sr/86Sr relative to fresh rock values (0.7024) and less enriched than the overlying sheeted dike complex. 87Sr/86Sr for the pervasively altered gabbroic samples ranges from 0.70244 to 0.70273 (mean 0.70257), tonalites is 0.7038, and pyroxene hornfels ranges from 0.70259 to 0.70271. 87Sr/86Sr does not vary with depth, and there is a strong positive correlation with the percentage of hydrous phases. Strontium contents of igneous and hydrothermal minerals, combined with bulk rock 87Sr/86Sr, indicate that Sr-isotopic exchange is largely controlled by the uptake of fluid 87Sr/86Sr in hydrous minerals and does not require Sr gain or loss. The minimum, time-integrated fluid-rock ratio for the sheeted dike complex and upper plutonics is 0.55-0.66, and the fluid flux calculated by mass balance is ~2.1 to 2.5 × 106 kg m-2, 30-60% higher than fluid fluxes calculated in the same manner

  15. Origin of Mesozoic and Tertiary granite in the western United States and implications for Pre-Mesozoic crustal structure: 2. Nd and Sr isotopic studies of unmineralized and Cu- and Mo-mineralized granite in the Precambrian Craton

    NASA Astrophysics Data System (ADS)

    Farmer, G. Lang; Depaolo, Donald J.

    1984-11-01

    magmas mixed with a lower crustal source with a significantly higher 87Sr/86Sr ratio. REE abundance patterns for metaluminous granite in the NGB are characterized by extreme LREE enrichment, which supports the proposed origin for these rocks by mantle/crust mixing or by remelting of the lower crust alone. No systematic difference exists between the sources of Cu- or Mo-mineralized and Unmineralized metaluminous granite, but the data suggest that the Cu sources are in the mantle and the Mo sources are in preexisting crust. Overall, the Nd data indicate that continental interior granite in the western United States was primarily derived from preexisting crust, and although changes in the thermal structure of the continental mantle may have triggered magma formation, the resulting granites do not represent significant juvenile additions to the continental crust.

  16. 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

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

    SciTech Connect

    B. Marshall; K. Futa

    2004-02-19

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

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

    NASA Astrophysics Data System (ADS)

    Marshall, B. D.; Futa, K.

    2004-05-01

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

  19. The Strontium Isotope Composition of Fossil Hackberry Seed Carbonate and Tooth Enamel as a Potential Record of Soil Erosion

    NASA Astrophysics Data System (ADS)

    Cooke, M. J.; Stern, L. A.; Banner, J. L.

    2001-12-01

    The Edwards Plateau in central Texas has experienced significant soil erosion since the Last Glacial Maximum. In contrast to the thin soils that mantle the Cretaceous limestone bedrock of the modern Edwards Plateau, Quaternary fossils of burrowing mammals contained within several central Texas cave deposits suggest soil cover was much thicker in the latest Pleistocene and early Holocene. As the landscape is denuded, the Cretaceous limestone bedrock is exhumed and becomes a more important source of exchangeable Sr to the soils. Therefore, the Sr isotope composition of the soil and organisms deriving nutrients from the soil, such as plants and herbivores, should become more like the Sr isotope composition of the bedrock as erosion continues. Because the marine limestone bedrock has a lower 87Sr/86Sr value than the soil, the exchangeable soil Sr should evolve to lower 87Sr/86Sr values through time resulting in a decrease in the 87Sr/86Sr of plants and animals deriving nutrients from the soil. In order to test this hypothesis, terrestrial fossils from an extensively dated Quaternary deposit within Hall's Cave, Kerr County, Texas were analyzed by TIMS for 87Sr/86Sr. The materials analyzed include aragonitic fossil hackberry seeds and rodent tooth enamel. Results indicate an overall decrease in the 87Sr/86Sr of fossil hackberry seed aragonite and rodent tooth enamel over the last 16,000 years, with the highest rate of decrease in the 87Sr/86Sr of fossil hackberry seeds (0.70982 to 0.70841) occurring between approximately 16,000 and 10,000 Y.B.P. This decrease in the 87Sr/86Sr is interpreted as evidence for an increase in the proportion of bedrock-derived Sr to the soils, corresponding to a general decrease in soil thickness. An increase in aridity or an increase in the seasonality of precipitation during this time could account for the post-glacial soil erosion in central Texas. This study suggests that the 87Sr/86Sr of fossils may be a useful proxy for paleo soil depth

  20. Constructing a Neoproterozoic Seawater Strontium Isotope Curve

    NASA Astrophysics Data System (ADS)

    Zhou, Y.; Shields-Zhou, G. A.; Manning, C. J.; Thirlwall, M.; Thurow, J. W.; Zhu, M.; Ling, H.

    2014-12-01

    The strontium isotopic composition of seawater has varied throughout Earth history in response to the balance between Sr isotopic exchange with ocean crust and input of riverine Sr derived from continental weathering. Because of this, seawater 87Sr/86Sr highs are interpreted to reflect erosion events, related to mountain building, while 87Sr/86Sr lows are considered to result from low weathering rates or increased seafloor spreading. Seawater 87Sr/86Sr also responds to changes in the isotopic composition of material undergoing weathering. The largest ever increase in seawater 87Sr/86Sr took place sometime from approximately 900 Ma to 500 Ma, and was associated with a permanent step shift in baseline 87Sr/86Sr composition. The unprecedented size of this increase, its timing and causation remains unconstrained. This study attempts firstly to reconstruct global seawater 87Sr/86Sr trends through this increase, using well-preserved carbonate rock samples from the North China craton, calibrated against additional 87Sr/86Sr and δ13C data from Neoproterozoic samples collected from other sections around the world. Sample preparation techniques for bulk carbonate Sr isotope stratigraphy are being honed during the course of this study. Other stable isotope systems (δ13C and δ18O) and trace elements, including REE have been investigated on the same samples to identify pristine samples for Sr isotope analysis and help in interpretation. The newly obtained data from this study (mainly Huaibei group of Huaibei area), using the excellently preserved early marine calcite cements and some bulk rock samples, confirm that the carbonate strata across the Jiao-Liao-Xu-Huai stratigraphic realm of the North China Craton exhibit the moderately positive δ13C values and low 87Sr/86Sr values that are characteristic of the early Neoproterozoic (Tonian).The results help to recreate the global curve by linking negative excursions in the Shijia (Xuzhou) (Xiao et al., 2014, Precambr. Res., 246

  1. Strontium isotopic variations of Neoproterozoic seawater: implications for crustal evolution.

    PubMed

    Asmerom, Y; Jacobsen, S B; Knoll, A H; Butterfield, N J; Swett, K

    1991-01-01

    We report high precision Sr isotopic data on carbonates from the Neoproterozoic Shaler Group, Victoria Island, Northwest Territories, Canada. Lithostratigraphic correlations with the relatively well-dated Mackenzie Mountains Supergroup constrain Shaler deposition to approximately 770-880 Ma, a range corroborated by 723 +/- 3 Ma lavas that disconformably overlie Shaler carbonates and by Late Riphean microfossils within the section. Samples with low 87Rb/86Sr ratios (<0.01) were selected for Sr isotopic analysis. Delta 18O, Mn, Ca, Mg, and Sr data were used to recognize altered samples. The altered samples are characterized by high Mn/Sr (> or = 2) and variable delta 18O; most are dolomites. The data indicate that between ca. 790-850 Ma the 87Sr/86Sr ratio of seawater varied between 0.70676 and 0.70561. The samples show smooth and systematic variation, with the lowest 87Sr/86Sr value of 0.70561 at ca. 830 Ma. The low 87Sr/86Sr ratio of carbonates from the lower parts of our section is similar to a value reported for one sample from the Adrar of Mauritania (approximately 900 Ma), West African Craton. Isotopic ratios from the upper part of the Shaler section are identical to values from the lower part of the Neoproterozoic Akademikerbreen Group, Spitsbergen. Although a paucity of absolute age determinations hinders attempts at the precise correlation of Neoproterozoic successions, it is possible to draw a broad outline of the Sr isotopic composition of seawater for this period. Indeed, the Sr isotope data themselves provide a stratigraphic tool of considerable potential. Data from this study and the literature are used to construct a curve of the 87Sr/86Sr ratio of Neoproterozoic seawater. The new data reported in this study substantially improve the isotopic record of Sr in seawater for the period 790-850 Ma. The Sr isotope composition of seawater reflects primarily the balance between continental Sr input through river input and mantle input via hydrothermal

  2. Strontium isotopic variations of Neoproterozoic seawater: implications for crustal evolution.

    PubMed

    Asmerom, Y; Jacobsen, S B; Knoll, A H; Butterfield, N J; Swett, K

    1991-01-01

    We report high precision Sr isotopic data on carbonates from the Neoproterozoic Shaler Group, Victoria Island, Northwest Territories, Canada. Lithostratigraphic correlations with the relatively well-dated Mackenzie Mountains Supergroup constrain Shaler deposition to approximately 770-880 Ma, a range corroborated by 723 +/- 3 Ma lavas that disconformably overlie Shaler carbonates and by Late Riphean microfossils within the section. Samples with low 87Rb/86Sr ratios (<0.01) were selected for Sr isotopic analysis. Delta 18O, Mn, Ca, Mg, and Sr data were used to recognize altered samples. The altered samples are characterized by high Mn/Sr (> or = 2) and variable delta 18O; most are dolomites. The data indicate that between ca. 790-850 Ma the 87Sr/86Sr ratio of seawater varied between 0.70676 and 0.70561. The samples show smooth and systematic variation, with the lowest 87Sr/86Sr value of 0.70561 at ca. 830 Ma. The low 87Sr/86Sr ratio of carbonates from the lower parts of our section is similar to a value reported for one sample from the Adrar of Mauritania (approximately 900 Ma), West African Craton. Isotopic ratios from the upper part of the Shaler section are identical to values from the lower part of the Neoproterozoic Akademikerbreen Group, Spitsbergen. Although a paucity of absolute age determinations hinders attempts at the precise correlation of Neoproterozoic successions, it is possible to draw a broad outline of the Sr isotopic composition of seawater for this period. Indeed, the Sr isotope data themselves provide a stratigraphic tool of considerable potential. Data from this study and the literature are used to construct a curve of the 87Sr/86Sr ratio of Neoproterozoic seawater. The new data reported in this study substantially improve the isotopic record of Sr in seawater for the period 790-850 Ma. The Sr isotope composition of seawater reflects primarily the balance between continental Sr input through river input and mantle input via hydrothermal

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

    USGS Publications Warehouse

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

    1978-01-01

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

  4. Crustal outgassing and LILE enrichment in major lithosphere structures, Archean Abitibi greenstone belt: evidence on the source reservoir from strontium and carbon isotope tracers

    NASA Astrophysics Data System (ADS)

    Kerrich, R.; Fryer, B. J.; King, R. W.; Willmore, L. M.; van Hees, E.

    1987-10-01

    Major structural discontinuities in the Abitibi greenstone belt acted as conduits for outgassing of the Archean crust, as reflected in fixation of a select group of lithophile elements including Si, C, K, Rb, Ba, Li, Cs, B and Pb, in metasomatized faults. For two of the largest structures, the Destor-Porcupine (DP) and Kirkland Lake — Cadillac (KC) fault zones ˜6×1015 g Si, 3×1015 g CO2 and 1015 g K were introduced into the faults during expulsion of an estimated 6×1018 g aqueous fluids. Strontium isotope ratios of tourmaline, piemontite, actinolite and scheelite mineral separates, characterized by Rb/Sr≤0.02, are concordant with respect to 87Sr/86Sr initial ratios over local sectors of the faults. The Sr isotope data record geographic variations which, from east to west on the KC fault is 0.7031 0.7041 (Val d'Or), 0.7008 0.7022 (Bourlemaque), 0.7017 0.7019 (Bousquet), 0.7029 0.7031 (Noranda), and 0.7013 to 0.7015 (Kirkland Lake). At Timmins, on the PD fault, 87Sr/86Sr initial ratios cluster at 0.7010 to 0.7020. Metasomatised fault zones are systematically more radiogenic than contiguous host lithologies, and imply a source reservoir (0.7010 to 0.7041) generally more radiogenic than the upper mantle at 2690 Ma (0.700±0.001), or contemporaneous volcanic rocks of mafic to ultramafic composition (0.700 to 0.7012). Whereas certain minerals are concordant and retentive, Rb-Sr isochrons based on suites of rocks at progressive intensities of metasomatism, have been systematically reset over an elpased time of ˜200 Ma after termination of outgassing, due to disturbance accompanying incremental displacements on structures. Carbon isotope compositions of ferroan dolomites in faults are tightly clustered along local fault sectors, but also display a marked provinciality: from east to west δ 13C=-6.0 to -8.5 (Malartic), -8.0 to -9.0 (Cadillac), -2.0 to -4.5 (Kirkland Lake), and -0.5 to -3.5 (Timmins). The observed provinciality of both δ 13C values and 87Sr/86Sr

  5. Sediment dewatering and pore fluid migration along thrust faults in a foreland basin inferred from isotopic and elemental geochemical analyses (Eocene southern Pyrenees, Spain)

    NASA Astrophysics Data System (ADS)

    Travé, Anna; Labaume, Pierre; Calvet, Francesc; Soler, Albert

    1997-12-01

    The lower Eocene Ainsa basin was formed during the first stages of the south-Pyrenean foreland basin evolution due to southwestward migration of imbricated thrust-folds. Isotopic and elemental geochemistry of syn-kinematic veins (calcite and celestite) and their marly host-rock, sampled in three thrust-fault zones and one footwall syncline, allows us to characterize the origin of pore fluids and the early stages of their evolution and circulation during the early deformation of the basin-fill. The isotopic composition of sulfur and the {87Sr }/{86Sr } ratios of calcites and celestites from the veins in the footwall syncline show that the original fluid had the isotopic composition of Eocene seawater. The different {87Sr }/{86Sr } ratio in veins from the thrust-fault zones compared with the same ratio in the marly host-rock of the footwall syncline indicates that the thrust-fault zones acted as conduits for advective fluids. The relatively high {87Sr }/{86Sr } ratio in the veins related to the thrust-fault zones indicates that the fluid originated from the interaction of seawater with an external fluid coming from deeper sources or from the meteoric weathering of the emerged part of the belt. δ 18O and δ 13C values of calcites show that the isotopic composition of the calcite-cements in veins was controlled by the isotopic composition of the marly host sediment. Depletion of both δ 18O and δ 13C with respect to Eocene seawater composition, together with elemental geochemistry of calcite cements in the veins, points to burial transformations of a seawater-derived fluid to a formation water composition. The distribution of δ 18O and δ 13C values of the marly host-rock and calcite cements in veins of the four outcrops probably resulted from differences in the meteoric water influences. The hydrogeological regime at the toe of the submarine thrust system was dominated by tectonically-induced dewatering of the foreland basin sediments. The thrust-fault zones were

  6. Middle Jurassic MORB-type gabbro, high-Mg diorite, calc-alkaline diorite and granodiorite in the Ando area, central Tibet: Evidence for a slab roll-back of the Bangong-Nujiang Ocean

    NASA Astrophysics Data System (ADS)

    Yan, Haoyu; Long, Xiaoping; Wang, Xuan-Ce; Li, Jie; Wang, Qiang; Yuan, Chao; Sun, Min

    2016-11-01

    Mesozoic intrusions, including MORB-type gabbros, high-Mg diorites, calc-alkaline diorites and granodiorites, were exposed in the Ando microcontinent that is bounded between the Qiangtang and Lhasa terranes. Discoveries of these Mesozoic intrusions have provided new petrogenetic constraints on our understanding of Bangong-Nujiang ocean evolution. Zircon U-Pb dating shows that these intrusions formed in the early-middle Jurassic (174-177 Ma). The gabbros have relatively flat REE distribution patterns, which is analogous to the geochemical features of MORB. Their positive εNd(t) values (εNd(t) = 4.4-5.5) are consistent with those of ophiolites along the Bangong-Nujiang suture zone. These gabbros are also characterized by enrichments of fluid-sensitive elements and negative to positive Nb anomalies, indicative of the influence of subduction-related compositions in their mantle source. These features suggest that the gabbros were most likely originated from asthenosphere-derived melts metasomatized by enriched lithospheric mantle during the upwelling. The high-Mg diorites are characterized by typical features of high compatible elements (MgO = 8.3-10.24 wt%, Cr = 400-547 ppm, Ni = 120-152 ppm), high Mg# (70-74) and low Sr/Y ratios. Their high initial 87Sr/86Sr isotopic ratios and negative εNd(t) values (- 10.5 to - 10.8), together with their sanukitic characteristics, imply that the high-Mg diorites were probably produced by partial melting of mantle peridotites metasomatized by slab-derived melts and aqueous fluids. The calc-alkaline diorites have relatively high MgO (4.04-5.50 wt%), Cr, Ni contents and Mg# (56-59), as well as high (86Sr/87Sr)i ratios and negative εNd(t) values (- 7.5 to - 7.3), suggesting that they were most likely formed by partial melting of the Ando basement rocks with significant input of mantle components. The granodiorites are peraluminous and have higher (86Sr/87Sr)i ratios and more negative εNd(t) values (- 10.6 to - 10.8), similar to

  7. Recognizing subtle evidence for silicic magma derivation from petrochemically-similar arc crust: Isotopic and chemical evidence for the bimodal volcanic series of Gorely Volcanic Center, Kamchatka, Russia

    NASA Astrophysics Data System (ADS)

    Seligman, A. N.; Bindeman, I. N.; Ellis, B. S.; Ponomareva, V.; Leonov, V.

    2012-12-01

    The Kamchatka Peninsula is home to some of the most prolific subduction related volcanic activity in the world. Gorely caldera and its central volcano are located in the rear of its currently active Eastern Volcanic Front. Recent work determined the presence of explosive ignimbrite eruptions sourced from Gorely volcano during the Pleistocene. We studied 32 eruptive units, including tephrochronologically-dated Holocene tephra, stratigraphically-arranged ignimbrites, as well as pre- and post-caldera lavas. We analyzed oxygen isotope ratios of pyroxene and plagioclase grains by laser fluorination, and major and trace element compositions of whole rocks. In addition, we determined 87Sr/86Sr and 143Nd/144Nd ratios of caldera-forming ignimbrite eruptions. Chemical compositions show that Gorely eruptive units range from basalt to basaltic andesite in the "Pra-Gorely" stages prior to caldera formation and the modern Gorely stages forming its current edifice. In contrast, eruptive material from earlier ignimbrites exposed at Opasny Ravine consists primarily of dacite. Whole rock analyses for Gorely indicate that silicic rocks and ignimbrites volumetrically dominate all other products, forming separate bimodal peaks in our SiO2-frequency diagram. In addition, trace element concentrations and ratios define two trends, one for more silicic and another for more mafic material. δ18Omelt values range from a low of 4.85 up to 6.22‰, where the lowest value was found in the last caldera forming eruption, suggesting incorporation of hydrothermally-altered material from earlier eruptions. 87Sr/86Sr and 143Nd/144Nd ratios range from 0.70328 to 0.70351 and from 0.51303 to 0.51309 respectively, with higher and more diverse values being characteristic of earlier ignimbrite units; again suggesting incorporation of surrounding crustal material. In contrast to these results, MELTS modeling using a variety of likely primitive basalts from Gorely shows it is possible to obtain silicic

  8. Pbsbnd Srsbnd Nd isotopic tracing of the influence of the Amazon River on the bottom sediments in the lower Tapajós River

    NASA Astrophysics Data System (ADS)

    Medeiros Filho, Lucio C.; Lafon, Jean-Michel; Souza Filho, Pedro Walfir M.

    2016-10-01

    The isotopic signatures of Pbsbnd Srsbnd Nd in recent bottom sediments were used to investigate the hydrodynamics of the lower stream of the Tapajós River and its interaction with the Amazon River. Samples from the Tapajós River have Pb isotopic ratios (19.67 < 206Pb/204Pb < 20.02; 15.87 < 207Pb/204Pb < 15.91) different from those of the bottom sediments found downstream in the Amazon River (18.84 < 206Pb/204Pb < 18.94; 207Pb/204Pb ≈ 15.67). In the confluence zone, the ratios have intermediate values (18.69 < 206Pb/204Pb < 19.53; 15.65 < 207Pb/204Pb < 15.83). The sediments in the Tapajós River have lower ɛNd(0) (-21 < ɛNd(0) < -19) values and more radiogenic isotopic Sr ratios (87Sr/86Sr ≈ 0.792) than those of the sediments from the Amazon River (ɛNd(0) ≈ -9 and 0.712 < 87Sr/86Sr < 0.716). The isotopic data suggest that the Amazon River influences the sediments in the Tapajós River, but this influence is restricted to the confluence zone. Additionally, the concentrations of major and trace elements and the mineralogy of the sediments are in agreement with the isotopic data. We conclude that the accumulation of muddy sediments in the lower stream of the Tapajós River is a result of the influence of the Amazon River, which retains this discharge from its affluent thus generating favorable conditions for depositing the finer sediments coming from the Tapajós River without any significant contribution of sediments from the Amazon River itself. The values of ɛNd(0) and TDM and of 87Sr/86Sr ratio of the Tapajós River bottom sediments indicate that the source of the sediments is essentially the erosion of the Paleoproterozoic felsic units from the Tapajós (2.03-1.88 Ga) and Juruena (1.82-1.54 Ga) geotectonic provinces.

  9. Identifying calcium sources at an acid deposition-impacted spruce forest: A strontium isotope, alkaline earth element multi-tracer approach

    USGS Publications Warehouse

    Bullen, T.D.; Bailey, S.W.

    2005-01-01

    Depletion of calcium from forest soils has important implications for forest productivity and health. Ca is available to fine feeder roots from a number of soil organic and mineral sources, but identifying the primary source or changes of sources in response to environmental change is problematic. We used strontium isotope and alkaline earth element concentration ratios of trees and soils to discern the record of Ca sources for red spruce at a base-poor, acid deposition-impacted watershed. We measured 87Sr/86Sr and chemical compositions of cross-sectional stemwood cores of red spruce, other spruce tissues and sequential extracts of co-located soil samples. 87Sr/86Sr and Sr/Ba ratios together provide a tracer of alkaline earth element sources that distinguishes the plant-available fraction of the shallow organic soils from those of deeper organic and mineral soils. Ca/Sr ratios proved less diagnostic, due to within-tree processes that fractionate these elements from each other. Over the growth period from 1870 to 1960, 87Sr/86Sr and Sr/Ba ratios of stemwood samples became progressively more variable and on average trended toward values that considered together are characteristic of the uppermost forest floor. In detail the stemwood chemistry revealed an episode of simultaneous enhanced uptake of all alkaline earth elements during the growth period from 1930 to 1960, coincident with reported local and regional increases in atmospheric inputs of inorganic acidity. We attribute the temporal trends in stemwood chemistry to progressive shallowing of the effective depth of alkaline earth element uptake by fine roots over this growth period, due to preferential concentration of fine roots in the upper forest floor coupled with reduced nutrient uptake by roots in the lower organic and upper mineral soils in response to acid-induced aluminum toxicity. Although both increased atmospheric deposition and selective weathering of Ca-rich minerals such as apatite provide possible

  10. Sediment Provenance in the Equatorial Atlantic and its Implications on Paleocirculation

    NASA Astrophysics Data System (ADS)

    Pahler, S. H.; Franzese, A. M.; Hemming, S. R.

    2005-12-01

    Ocean circulation in the Equatorial Atlantic is composed of a diverse range of currents from the surface level equatorial currents and countercurrents to the North Atlantic Deep Water (NADW). Sediments deposited in this region are derived from Africa and South America by a combination of aeolian and fluvial pathways and then transported by ocean currents. Fifteen cores from the Equatorial Atlantic (10°N to 10°S, 0° to 45°W) were used to determine sediment provenance during the Holocene and Last Glacial Maximum (LGM), and specifically to test whether sediment was transported by surface or deep water currents. The radiogenic isotopic composition of any rock depends on its age, initial composition and its geologic history. The strontium isotopic composition of the terrigenous portion of marine sediments can often be used to identify the source rock(s) from which they weathered. By incorporating this new sediment core data from both Holocene and LGM depths with previous research designating the 87Sr/86Sr ratios for source areas in Africa and South America we were able to connect possible source areas with core locations. In general, the 87Sr/86Sr ratios from the Holocene are higher than those from the LGM, indicating a greater contribution from geologically older sediment sources during the Holocene. Primary sediment transport from African sources is best explained by wind transport, while sediment derived from South American sources is most easily explained by river input. The geographic pattern of 87Sr/86Sr ratios appears to be correlated to deep ocean circulation, specifically the NADW which flows southward along the western side of the Atlantic near South America and then cuts east along the Romanche Fracture Zone (RFZ, ~0°) before continuing south once again in the eastern basin near Africa. Based on our results, there is no observable difference in transport mechanisms between the Holocene and LGM; however, the difference in ratios between the two time

  11. 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

  12. Chemical and strontium isotope characterization of rainwater in Beijing during the 2008 Olympic year

    NASA Astrophysics Data System (ADS)

    Xu, Zhifang; Tang, Yang; Ji, Jianpeng

    2012-04-01

    To improve the air quality during the 2008 Beijing Olympic Games, the Beijing Municipal Government enforced a series of emission control measures. This provided a valuable case study to evaluate the effectiveness of these aggressive measures on mitigating air pollution and improving the atmospheric environment. In this paper, we report the first results of the chemical and Sr isotopic compositions of the rainwater in Beijing during the 2008 Olympic year. The ionic composition of samples show that Ca2 + and NH4+ were the dominant cations, accounting for about 76-97% of the total cations, and that SO42 - and NO3- were the major anions, accounting for 61-91% of the total anions measured. Using Na as the indicator of marine origin and Al as that of terrestrial inputs, the proportions of sea salt and terrestrial elements were estimated from elemental ratios. The calculated results indicate that the major chemical components were mainly of non-sea-salt origin. Good correlation between Ca2 + and Sr2 + (R2 = 0.85) in rainwater samples indicates the potential of Sr as a provenance tracer for Ca. Sr2 + concentrations in rainwater samples ranged from 0.01 to 2.87 μmol l- 1, with 87Sr/86Sr ratios from 0.7092 to 0.7109. All of the samples had a 87Sr/86Sr ratio higher than that of seawater. The 87Sr/86Sr isotopic and elemental ratio systems show that the data set of rainwater was mainly distributed between the seawater end-member (~ 0.70917) and the soil dust end-member (0.7111-0.7115), and the analysis indicate that the effect of anthropogenic inputs could decrease in 2008. Comparisons of the chemical composition of the rainwater in different periods show that all chemical components, except NH4+, had the lowest concentration levels during the Olympic Game period. The VWM concentrations of major ions in the rainwater decreased significantly during the Olympic period by up to 29% for SO42 -, 39% for NO3-, 38% for Ca2 +, 51% for Mg2 +, 57% for K+, and 44% for Na+, compared with

  13. Geochemistry of ultrapotassic volcanic rocks in Xiaogulihe NE China: Implications for the role of ancient subducted sediments

    NASA Astrophysics Data System (ADS)

    Sun, Yang; Ying, Jifeng; Zhou, Xinhua; Shao, Ji'an; Chu, Zhuyin; Su, Benxun

    2014-11-01

    The unique eruptions of ultrapotassic volcanic rocks in eastern China reported so far took place in the Xiaogulihe area of western Heilongjiang Province, NE China. These ultrapotassic rocks are characterized by extremely high K2O contents (> 7 wt.%), abnormally unradiogenic Pb isotopic compositions (206Pb/204Pb = 16.44-16.55; 207Pb/204Pb = 15.39-15.46; 208Pb/204Pb = 36.35-36.61), and moderately high 87Sr/86Sr ratios (0.7053-0.7057), which can be basically correlated with those of ultrapotassic igneous rocks distributed widely in northwestern America and Aldan Shield. The positive correlation between 187Os/188Os and 1/Os argues that these ultrapotassic rocks have probably experienced negligible lower continental crust addition (less than 1%) during magma ascent. The high contents of K2O and negative correlation between 87Sr/86Sr and 206Pb/204Pb of these ultrapotassic rocks indicate the presence of a potassic phase, mostly phlogopite, in their mantle source. Their strong fractionation of rare earth elements and lack of Nd-Hf isotopic decoupling reveal a low-degree partial melting of garnet-bearing source rocks. In addition, the low CaO and Al2O3 contents of whole-rock compositions and low Fe/Mn ratios of olivine phenocryst chemistries suggest peridotites rather than pyroxenites as dominant source rocks for the Xiaogulihe ultrapotassic rocks. Based on these distinctive geochemical characteristics, we thus propose that the ultimate mantle source of the Xiaogulihe ultrapotassic volcanic rocks is phlogopite-bearing garnet peridotite within the lower part of the sub-continental lithospheric mantle (SCLM) that had been metasomatized by potassium-rich silicate melts. Combined with the unradiogenic Pb compositions, the most likely source of these potassium-rich silicate melts is the ancient subducted continental-derived sediments (> 1.5 Ga). These ancient subducted sediments, possessing relatively low initial Pb isotopic compositions, had experienced large U/Pb fractionation

  14. Zircon U-Pb age, Hf isotopic compositions and geochemistry of the Silurian Fengdingshan I-type granite Pluton and Taoyuan mafic-felsic Complex at the southeastern margin of the Yangtze Block

    NASA Astrophysics Data System (ADS)

    Zhong, Yufang; Ma, Changqian; Zhang, Chao; Wang, Shiming; She, Zhenbing; Liu, Lei; Xu, Haijin

    2013-09-01

    This work presents an integrated study of zircon U-Pb ages and Hf isotope along with whole-rock geochemistry on Silurian Fengdingshan I-type granites and Taoyuan mafic-felsic intrusive Complex located at the southeastern margin of the Yangtze Block, filling in a gap in understanding of Paleozoic I-type granites and mafic-intermediate igneous rocks in the eastern South China Craton (SCC). The Fengdingshan granite and Taoyuan hornblende gabbro are dated at 436 ± 5 Ma and 409 ± 2 Ma, respectively. The Fengdingshan granites display characteristics of calc-alkaline I-type granite with high initial 87Sr/86Sr ratios of 0.7093-0.7127, low ɛNd(t) values ranging from -5.6 to -5.4 and corresponding Nd model ages (T2DM) of 1.6 Ga. Their zircon grains have ɛHf(t) values ranging from -2.7 to 2.6 and model ages of 951-1164 Ma. The Taoyuan mafic rocks exhibit typical arc-like geochemistry, with enrichment in Rb, Th, U and Pb and depletion in Nb, Ta. They have initial 87Sr/86Sr ratios of 0.7053-0.7058, ɛNd(t) values of 0.2-1.6 and corresponding T2DM of 1.0-1.1 Ga. Their zircon grains have ɛHf(t) values ranging from 3.2 to 6.1 and model ages of 774-911 Ma. Diorite and granodiorite from the Taoyuan Complex have initial 87Sr/86Sr ratios of 0.7065-0.7117, ɛNd(t) values from -5.7 to -1.9 and Nd model ages of 1.3-1.6 Ga. The petrographic and geochemical characteristics indicate that the Fengdingshan granites probably formed by reworking of Neoproterozoic basalts with very little of juvenile mantle-derived magma. The Taoyuan Complex formed by magma mixing and mingling, in which the mafic member originated from a metasomatized lithospheric mantle. Both the Fengdingshan and Taoyuan Plutons formed in a post-orogenic collapse stage in an intracontinental tectonic regime. Besides the Paleozoic Fengdingshan granites and Taoyuan hornblende gabbro, other Neoproterozoic and Indosinian igneous rocks located along the southeastern and western margin of the Yangtze Block also exhibit decoupled

  15. Origin of dolomites in the Cretaceous Maha Sarakham evaporites of the Khorat Plateau, northeast Thailand

    NASA Astrophysics Data System (ADS)

    El Tabakh, Mohamed; Utha-Aroon, Cherdsak; Warren, John K.; Schreiber, B. Charlotte

    2003-04-01

    The Khorat Plateau of northeast Thailand and Laos was an area of widespread deposition of evaporites and siliciclastics (Maha Sarakham Formation) during the Cretaceous and three types of dolomites are associated with this formation: (1) limpid dolomite, (2) coarse, subhedral and euhedral dolomite, and (3) saddle dolomite. Limpid dolomite is present as isolated crystals in recrystallized, clear halite beds while the other two types are only present as authigenic clusters and individual large crystals within the widespread Basal Anhydrite Unit (BAU) (1.1 m), which defines the lowest member of the formation. The δ18O PDB isotopic values and the 87Sr/ 86Sr ratios of the limpid dolomite are within the range of Cretaceous seawater. Petrography and carbon and oxygen isotopes suggest that limpid dolomite was formed under shallow burial during times of freshening in a mostly marine-fed aggrading halite salina. Dolomite formation was possibly influenced by bacterial metabolism. The coarse crystalline and saddle dolomite types float within a matrix of coarse, recrystallized anhydrite in the Basal Anhydrite. The δ18O isotopic values of the coarse, subhedral and euhedral dolomite types are more negative than the limpid dolomite, and the 87Sr/ 86Sr ratios are more radiogenic than typical marine dolomite of the Cretaceous. Saddle dolomite has even more negative δ18O isotopic values than the coarse euhedral dolomite. The 87Sr/ 86Sr ratios of the saddle dolomite are also radiogenic. The isotopic and petrographic data indicate that the dolomites in the Basal Anhydrite Unit are late and authigenic but do not appear to replace a precursor carbonate. Rather, they appear to have precipitated within the deep burial environment along a 1-2-m-thick subsurface mixing interface between warm upwelling basinal brines and dense highly saline brines created by dissolving the underside of the overlying impervious halite bed. The upwelling basinal waters presumably rose through the underlying

  16. 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

  17. 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

  18. 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

  19. Magma mixing in the genesis of the Kalatongke dioritic intrusion: Implications for the tectonic switch from subduction to post-collision, Chinese Altay, NW China

    NASA Astrophysics Data System (ADS)

    Gao, Jian-Feng; Zhou, Mei-Fu

    2013-03-01

    The Kalatongke complex, located in south Chinese Altay of the Central Asian Orogenic Belt (CAOB), consists of the ~ 308 Ma dioritic suite intruded by the 287 Ma noritic suite. The noritic suite is composed of olivine norite and hornblende norite and hosts sulfide mineralization. The dioritic suite is composed of ferrodiorite, diorite and quartz diorite. Ferrodiorites have 43.6 to 51.8 wt.% SiO2, 8.2 to 12.1 wt.% Fe2O3T, 2.87 to 4.86 wt.% MgO, with Mg# ranging from 42 to 53. They have highly variable Al2O3 (17.4-20.7 wt.%), Na2O (2.78-4.50%), K2O (0.58-3.70%), Sr (280-1300 ppm) and Ba (219-3100 ppm). Diorites and quartz diorites have 15.2-19.6 wt.% Al2O3, 239-890 ppm Sr and170-1100 ppm Ba, 11.2-25.5 ppm Y and1.2-2.2 ppm Yb. All rocks have LREE enriched REE patterns and do not display Eu anomalies. They have primitive mantle-normalized trace element patterns enriched in large ion lithosphile elements (LILE) (e.g. Ba and Sr) and depleted in Ti, Nb and Ta. Both ferrodiorites and diorites have relatively constant initial 87Sr/86Sr ratios of 0.7037 to 0.7040 but highly variable ɛNd(t) values of + 4.5 to + 11.6, whereas quartz diorites have higher initial 87Sr/86Sr ratios (0.7056) and lower ɛNd(t) values (+ 0.5). Plagioclase from ferrodiorites, diorites and quartz diorites has similar initial 87Sr/86Sr ratios of 0.7015 to 0.7055. The dioritic suite formed from a mixed magma of an evolved mantle-derived basaltic magma by partial melting of subduction-modified mantle source in response to slab breakoff and a crustal-derived granitic magma at ~ 308 Ma. Before mixing with granitic magmas, basaltic magmas underwent fractional crystallization of olivine to form ferrodiorite. The mixed magma also formed diorite and quartz diorite combining fractionation clinopyroxene, amphibole and plagioclase. The noritic suite formed from a mantle-derived high-Mg magma in a post-collisional environment. Both the dioritic and noritic suites in Kalatongke suggest the switch from subduction to

  20. Strontium isotope and major ion chemistry of the rainwaters from Guiyang, Guizhou Province, China.

    PubMed

    Han, Guilin; Liu, Cong-Qiang

    2006-07-01

    Twenty-two rainwater samples from Guiyang city, southwestern China, have been analyzed for their chemical compositions and 87Sr/86Sr ratios, with a main purpose to get a better understanding of the general features of rainwater in Guiyang city and their correspondences to human activities. The rainwaters studied are almost acidic (pH=4.53) and show big changes in major ion composition. Ca2+ and Mg2+ are the principal cations in the rainwaters and their mean values are 56.6 micromol/L (12.5-163.8 micromol/L) and 12.8 micromol/L (4.5-47.3 micromol/L ), respectively. The sum of Ca2+ and Mg2+ accounts for 78%-96% of the total cations in the studied rainwaters. Na+ was the least abundant of the major cations with a mean content of 4 micromol/L (0.9-7.8 micromol/L). SO4(2-) is the predominant anion, with a mean content of 94 micromol/L (33.5-279.4 micromol/L), coming next is NO(3-) with a mean content of 48 micromol/L (2.1-251.8 micromol/L). SO4(2-) and NO(3-) together account for 77%-99% of the total anions. Ca2+ and Mg2+ in the rainwater are most likely from dissolution of carbonate minerals in dust or aerosol, unlike K+ that shows more contribution of anthropogenic sources to the rainwater. Na+ does not vary in concentration with Cl-. Significant enrichment of Cl- relative to Na+ as compared with sea water indicates negligible contribution of marine source, which is supported by the evidence that the total rainwater samples show lower 87Sr/86Sr ratios (ranging from 0.707934 to 0.709080) than sea water. The rainwater samples are characterized by high contents of NO(3-), SO4(2-), and Cl- relative to Na+, as compared to the rainwater from other areas in the world, suggesting that the anions (NO(3-), SO4(2-), and Cl-) have mainly of anthropogenic sources. Sr isotope shows potential to trace sources of contaminants when combined with other chemical factors: covariation of 87Sr/86Sr ratio with Cl-/Na+ in the rainwater suggest presence of at least two anthropogenic sources

  1. Geochemical and Sr Nd Pb isotopic evidence for a combined assimilation and fractional crystallisation process for volcanic rocks from the Huichapan caldera, Hidalgo, Mexico

    NASA Astrophysics Data System (ADS)

    Verma, Surendra P.

    2001-03-01

    This study reports new geochemical and Sr-Nd-Pb isotopic data for Miocene to Quaternary basaltic to andesitic, dacitic, and rhyolitic volcanic rocks from the Huichapan caldera, located in the central part of the Mexican Volcanic Belt (MVB). The initial Sr and Nd isotopic ratios, except for one rhyolite, range as follows: 87Sr/ 86Sr 0.70357-0.70498 and 143Nd/ 144Nd 0.51265-0.51282. The Sr-Nd-Pb isotopic ratios are generally similar to those for volcanic rocks from other areas of the central and eastern parts of the MVB. The isotopic ratios of one older pre-caldera rhyolite (HP30) from the Huichapan area, particularly its high 87Sr/ 86Sr, are significantly different from rhyolitic rocks from this and other areas of the MVB, but are isotopically similar to some felsic rocks from the neighbouring geological province of Sierra Madre Occidental (SMO), implying an origin as a partial melt of the underlying crust. The evolved andesitic to rhyolitic magmas could have originated from a basaltic magma through a combined assimilation and fractional crystallisation (AFC) process. Different compositions, representing lower crust (LC) and upper crust (UC) as well as a hypothetical crust similar to the source of high 87Sr/ 86Sr rhyolite HP30, were tested as plausible assimilants for the AFC process. The results show that the UC represented by granitic rocks from a nearby Los Humeros area or by Cretaceous limestone (L) rocks outcropping in the northern part of the study area, and the LC represented by granulitic xenoliths from a nearby San Luis Potosı´ (SLP) area are not possible assimilants for Huichapan magmas, whereas a hypothetical crust (HA) similar in isotopic compositions to rhyolite HP30 could be considered a possible assimilant for the AFC process. Chemical composition of assimilant HA, although not well constrained at present, was inferred under the assumption that HP30 type partial melts could be generated from its partial melting. These data were then used to evaluate

  2. Geochemistry and geochronology of mafic rocks from the Luobusa ophiolite, South Tibet

    NASA Astrophysics Data System (ADS)

    Zhang, Chang; Liu, Chuan-Zhou; Wu, Fu-Yuan; Zhang, Liang-Liang; Ji, Wei-Qiang

    2016-02-01

    This study presents geochemical compositions of mafic rocks outcropped in the Luobusa ophiolite that locates at the eastern part of the Yarlung Zangbo Suture Zone (YZSZ). The studied mafic rocks include gabbroic/diabase dykes cutting the peridotites and foliated amphibolites embedded within the subophiolitic mélange. The diabases have low K2O contents and display N-MORB-like geochemical characteristics, i.e., with flat REE patterns and weak enrichment in LILE (e.g., Rb, Ba, Th and U). The gabbros show LREE-depleted patterns and variable enrichment in Rb and Ba. Foliated amphibolites mainly consist of hornblendes and plagioclases, with minor titanites. They commonly show LREE-depleted patterns, with strong enrichment in LILE. Three diabases have depleted Sr-Nd-Hf isotope compositions, with initial 87Sr/86Sr ratios of 0.703009-0.703502, εNd(t) of + 5.0 to + 8.5 and εHf (t) of ca + 14. Two gabbros have similar Nd-Hf isotopes with the diabases, but slightly higher initial 87Sr/86Sr ratios (i.e., 0.704820 and 0.704550). Compared to both diabases and gabbros, the amphibolites have higher initial 87Sr/86Sr ratios (i.e., 0.705131-0.705825), but more depleted Nd-Hf isotope compositions, with εNd(t) of + 9.1 to + 11.6 and εHf(t) of + 18.2 to + 21.9. Geochemical compositions of the diabase dykes indicate that they were formed in a mid-ocean ridge setting. Zircon SIMS U-Pb dating of the gabbroic dyke cutting the serpentinites yields an age of 128.4 ± 0.9 Ma, which is identical within uncertainty to the zircon U-Pb age of the amphibolite (i.e., 131.0 ± 1.2 Ma). Low U and Th contents of zircons in the amphibolite support their metamorphic origin. Titanites in the amphibolites have been dated by LA-ICPMS and give U-Pb ages of ~ 131-134 Ma, which are similar to the zircon U-Pb ages of the dated gabbro and amphibolite. Therefore, we suggest that the Luobusa ophiolite was generated at the Early Cretaceous and underwent the intra-oceanic emplacement immediately after its

  3. Complex metasomatism of lithospheric mantle by asthenosphere-derived melts: Evidence from peridotite xenoliths in Weichang at the northern margin of the North China Craton

    NASA Astrophysics Data System (ADS)

    Zou, Dongya; Zhang, Hongfu; Hu, Zhaochu; Santosh, M.

    2016-11-01

    The petrology, in situ analyses of major and trace elements as well as Sr isotopic compositions of spinel-facies lherzolite and harzburgite xenoliths from Weichang within the northern margin of the North China Craton (NCC) are reported for the first time in this study to evaluate the nature and evolution of the lithospheric mantle. These peridotite xenoliths display porphyroclastic texture and can be subdivided into two groups. Group I peridotites have slightly higher forsterite contents (Fo) (90.6-91.2) and 87Sr/86Sr ratios (0.7025-0.7043) in the cores than those in the rims (89.8-90.8; 0.7025-0.7038) of olivines and clinopyroxenes, respectively. The clinopyroxenes in these rocks exhibit uniform LREE-depleted patterns. These geochemical features suggest that the Group I peridotites were weakly metasomatized by recent asthenospheric melts. In contrast, Group II peridotites show sieve-texture and clear compositional zoning in minerals. The olivines and clinopyroxenes from these rocks have higher Fo (86.9-91.3) and 87Sr/86Sr ratios (0.7035-0.7049) in the cores than those in the rims (76.9-90.6; 0.7021-0.7046). The clinopyroxenes show three types of REE patterns: LREE-enriched, convex-upward and spoon-shaped. The LREE-enriched clinopyroxenes have the highest (La/Yb)N and lowest Ti/Eu and those with spoon-shaped REE patterns show an increase in LREE, Ba, Th and U contents from the cores to the rims. These features indicate that the Group II peridotites witnessed a high degree of refertilization by recent asthenosphere-derived silicate and carbonatite melts or their mixture. Compared with the data of the Mesozoic NCC lithospheric mantle, the heterogeneous and low 87Sr/86Sr ratios (0.7025-0.7049) in the LREE-depleted clinopyroxenes reveal that the ancient lithospheric mantle could have been modified by asthenospheric melts before the recent metasomatism event. We conclude that the lithospheric mantle beneath Weichang underwent multiple modifications through asthenosphere

  4. A geochemical approach for the evaluation of water availability and salinity in closed basins: the Draa Basin, Morocco

    NASA Astrophysics Data System (ADS)

    Warner, N.; Lgourna, Z.; Boutaleb, S.; Tagma, T.; Vinson, D. S.; Ettayfi, N.; Bouchaou, L.; Vengosh, A.

    2010-12-01

    In the sub-Saharan Draa Basin of southern Morocco, winter snowmelt from the Atlas Mountains is captured in a reservoir, stored, and discharged downstream for irrigation in six oases. The combined imported surface water and shallow groundwater exploitation for sustaining local agriculture is a common practice in many worldwide arid basins.. Like in many basins, the salinization of groundwater in the Draa Basin has become a limiting factor for agricultural development and long-term sustainability. .Since most of the IPCC climate models predict a significant decrease in precipitation in Northern Africa over the next few decades, water shortage and salinization induced from climate change are expected to exacerbate the existing water crisis. Evaluating the sources and mechanisms of this salinization can provide the necessary tools for sustainable water management in the Draa Basin that may be applied to many similarly arid basins. Here we present new geochemical results from 98 shallow groundwater and four surface water samples collected in May 2009 and April 2010. The samples were collected from upstream tributaries to the reservoir, the reservoir, and groundwater from in six oases downstream of the reservoir. The goal of the survey was to identify the sources of salinity using geochemical and isotopic (87Sr/86Sr, δ2H, and δ18O) signatures in the groundwater, which could derive from three possible sources (1) evaporation and recycling of the irrigation water; (2) dissolution of salts that were entrapped in the unsaturated zone; and (3) lateral flow of adjacent groundwater. The data show a large salinity range from fresh water to highly brackish water with total dissolved salts (TDS) exceeding 12,000 mg/L. The salinity increases with downstream flow between successive oases. Br/Cl and B/Cl ratios decrease with TDS, which suggests that the main mechanism of salinization in the Draa Basin is derived salt dissolution in the unsaturated zone and salinization of the

  5. Evaluation of the Impacts of Marine Salts and Asian Dust on the Forested Yakushima Island Ecosystem, a World Natural Heritage Site in Japan.

    PubMed

    Nakano, Takanori; Yokoo, Yoriko; Okumura, Masao; Jean, Seo-Ryong; Satake, Kenichi

    2012-11-01

    To elucidate the influence of airborne materials on the ecosystem of Japan's Yakushima Island, we determined the elemental compositions and Sr and Nd isotope ratios in streamwater, soils, vegetation, and rocks. Streamwater had high Na and Cl contents, low Ca and HCO(3) contents, and Na/Cl and Mg/Cl ratios close to those of seawater, but it had low pH (5.4 to 7.1), a higher Ca/Cl ratio than seawater, and distinct (87)Sr/(86)Sr ratios that depended on the bedrock type. The proportions of rain-derived cations in streamwater, estimated by assuming that Cl was derived from sea salt aerosols, averaged 81 % for Na, 83 % for Mg, 36 % for K, 32 % for Ca, and 33 % for Sr. The Sr value was comparable to the 28 % estimated by comparing Sr isotope ratios between rain and granite bedrock. The soils are depleted in Ca, Na, P, and Sr compared with the parent materials. At Yotsuse in the northwestern side, plants and the soil pool have (87)Sr/(86)Sr ratios similar to that of rainwater with a high sea salt component. In contrast, the Sr and Nd isotope ratios of soil minerals in the A and B horizons approach those of silicate minerals in northern China's loess soils. The soil Ca and P depletion results largely from chemical weathering of plagioclase and of small amounts of apatite and calcite in granitic rocks. This suggests that Yakushima's ecosystem is affected by large amounts of acidic precipitation with a high sea salt component, which leaches Ca and its proxy (Sr) from bedrock into streams, and by Asian dust-derived apatite, which is an important source of P in base cation-depleted soils.

  6. Oxygen and strontium isotopic studies of basaltic lavas from the Snake River plain, Idaho

    USGS Publications Warehouse

    Leeman, William P.; Whelan, Joseph F.

    1983-01-01

    The Snake Creek-Williams Canyon pluton of the southern Snake Range crops out over an area of about 30 km2, about 60 km southeast of Ely, Nev. This Jurassic intrusion displays large and systematic chemical and mineralogical zonation over a horizontal distance of 5 km. Major-element variations compare closely with Dalyls average andesite-dacite-rhyolite over an SiO2 range of 63 to 76 percent. For various reasons it was originally thought that assimilation played a dominant role in development of the Snake Creek-Williams Canyon pluton. However, based on modeling of more recently obtained trace element and isotopic data, we have concluded that the zonation is the result of in-situ fractional crystallization, with little assimilation at the level of crystallization. This report summarizes data available for each of the mineral species present in the zoned intrusion. Special attention has been paid to trends We present oxygen and strontium isotopic data for olivine tholeiites, evolved (that is, differentiated and (or) contaminated) lavas, rhyolites, and crustal- derived xenoliths from the Snake River Plain. These data show that the olivine tholeiites are fairly uniform in d80 (5.1 to 6.2) and 87Sr/86Sr (0.7056 to 0.7076) and reveal no correlation between these ratios. The tholeiites are considered representative of mantle-derived magmas that have not interacted significantly with crustal material or meteoric water. The evolved lavas display a wider range in d 80 (5.6 to 7.6) and 87Sr/86Sr (0.708 to 0.717) with positive correlations between these ratios in some suites but not in others. Crustal xenoliths have high and variable 8?Sr/86Sr (0.715 to 0.830) and d80 values that vary widely (6.7 to 9.2) and are a few permil greater than d80 values of the Snake River basalts. Thus, isotopic data for the evolved lavas are permissive of small degrees of contamination by crustal rocks similar to the most d80-depleted xenoliths. The d80 enrichments in some evolved lavas also are

  7. Tracing the chemical evolution of fluids during hydrothermal recharge: Constraints from anhydrite recovered in ODP Hole 504B

    NASA Astrophysics Data System (ADS)

    Teagle, Damon A. H.; Alt, Jeffrey C.; Halliday, Alex N.

    1998-02-01

    A unique record of the chemical evolution of seawater during hydrothermal recharge into oceanic crust is preserved by anhydrite from the volcanic sequences and sheeted dike complex in ODP Hole 504B. Chemical and isotopic analyses ( 87Sr/ 86Sr, δ18O, δ34S) of anhydrite constrain the changing composition of fluids due to reaction with basalt. There is a general trend of decreasing 87Sr/ 86Sr of anhydrite, corresponding to the minor incorporation of basaltic strontium with depth in the volcanic rocks. 87Sr/ 86Sr ratios decrease rapidly with depth in the dikes to values identical to host basalt (0.7029). Sr/Ca ratios (<0.1 mmol/mol) suggest that recharge fluids have very low Sr concentrations and fluids evolve by first precipitating Sr-bearing phases before extensive exchange of Sr with the host basalt. There is a background trend of decreasing sulfate δ18O with depth from +12-13‰ in the lower volcanics to +7‰ in the lower sheeted dikes recording an increase in recharge fluid temperature from ≈150° to ≈250°C, and confirming the presence of sulfate in hydrothermal fluids at elevated temperatures. From the amount of anhydrite recovered from Hole 504B and the amount of seawater sulfur that has been reduced to sulfide, a minimum seawater recharge flux can be calculated. This value is ≈4-25 times lower than estimates of high-temperature fluid fluxes based on either thermal constraints or global chemical budgets and suggests that there is significant deficit of seawater-derived sulfur in the oceanic crust. Only a minor proportion of the seawater that percolates into the crust near the axis is heated to high temperatures and exits as black smoker-type fluids. A significant proportion of the axial heat loss must be advected at 200-250°C by sulfate-bearing hydrothermal solutions that egress diffusely from the crust. These fluids penetrate into the dikes and exchange both heat and chemical tracers without the extensive clogging of porosity by anhydrite

  8. Climatic and tectonic controls on chemical weathering in the New Zealand Southern Alps

    NASA Astrophysics Data System (ADS)

    Jacobson, Andrew D.; Blum, Joel D.; Chamberlain, C. Page; Craw, Dave; Koons, Peter O.

    2003-01-01

    Climatic and tectonic controls on the relative abundance of solutes in streams draining the New Zealand Southern Alps were investigated by analyzing the elemental and Sr isotope geochemistry of stream waters, bedload sediment, and hydrothermal calcite veins. The average relative molar abundance of major cations and Si in all stream waters follows the order Ca 2+ (50%) > Si (22%) > Na + (17%) > Mg 2+ (6%) > K + (5%). For major anions, the relative molar abundance is HCO 3- (89%) > SO 42- (7%) > Cl - (4%). Weathering reactions involving plagioclase and volumetrically small amounts of hydrothermal calcite define the ionic chemistry of stream waters, but nearly all streams have a carbonate-dominated Ca 2+ and HCO 3- mass-balance. Stream water Ca/Sr and 87Sr/ 86Sr ratios vary from 0.173 to 0.439 μmol/nmol and from 0.7078 to 0.7114, respectively. Consistent with the ionic budget, these ratios lie solely within the range of values measured for bedload carbonate (Ca/Sr = 0.178 to 0.886 μmol/nmol; 87Sr/ 86Sr = 0.7081 to 0.7118) and hydrothermal calcite veins (Ca/Sr = 0.491 to 3.33 μmol/nmol; 87Sr/ 86Sr = 0.7076 to 0.7097). Streams draining regions in the Southern Alps with high rates of physical erosion induced by rapid tectonic uplift and an extremely wet climate contain ˜10% more Ca 2+ and ˜30% more Sr 2+ from carbonate weathering compared to streams draining regions in drier, more stable landscapes. Similarly, streams draining glaciated watersheds contain ˜25% more Sr 2+ from carbonate weathering compared to streams draining non-glaciated watersheds. The highest abundance of carbonate-derived solutes in the most physically active regions of the Southern Alps is attributed to the tectonic exhumation and mechanical denudation of metamorphic bedrock, which contains trace amounts of calcite estimated to weather ˜350 times faster than plagioclase in this environment. In contrast, regions in the Southern Alps experiencing lower rates of uplift and erosion have a greater

  9. Carbonate reactions in a natural CO2 Reservoir, Green River, Utah, USA

    NASA Astrophysics Data System (ADS)

    Chapman, H.; Bickle, M. J.; Kampman, N.; Maskell, A.; Busch, A.; Evans, J. P.

    2013-12-01

    -isotopic compositions of the Mg-Ca-Fe carbonate and Fe-rich minerals within the reservoir and cap rocks. These phases result from both diagenesis and subsequent reactions with CO2-charged brines. The Navajo rock samples have higher 87Sr/86Sr ratios in the silicate and carbonate fractions than those of the underlying formations and overlying caprock. The correlation between 87Sr/86Sr ratios and dissolved CO2 in the downhole fluid samples indicates that the more CO2-enriched fluids exhibit higher degrees of fluid:rock interaction with the Navajo sandstone.

  10. IODP Expedition 345: Characterizing Hydrothermal Alteration of Fast-Spreading EPR Lower Crust using O, Sr and Nd isotopics

    NASA Astrophysics Data System (ADS)

    Marks, N.; Gillis, K. M.; Lindvall, R. E.; Schorzman, K.

    2014-12-01

    The Integrated Ocean Drilling Program (IODP) Expedition 345 sampled lower crustal primitive gabbroic rocks that formed at the fast-spreading East Pacific Rise (EPR) and are exposed at the Hess Deep Rift. The metamorphic mineral assemblages in the rocks recovered at Site U1415 record the cooling of primitive gabbroic lithologies from magmatic (>1000°C) to zeolite facies conditions (<200°C) associated with EPR spreading, Cocos-Nazca rifting and exposure onto the seafloor. The dominant alteration assemblage is characterized by lower grade greenschist (<400°C) and subgreenschist facies (<200°C) alteration of olivine to talc, serpentine, or clay minerals, and is commonly accompanied by prehnite microveins in plagioclase. The intensity of alteration varies with igneous lithology, in particular, the modal abundance of olivine, as well as proximity to zones of brittle fracturing and cataclasis. We have attempted to characterize the nature and extent of isotopic exchange associated alteration and cooling and present a record of variations in O, Sr, and Nd isotopic compositions in altered rocks from the lower plutonic crust at Hess Deep. The Rb-Sr and 18O/16O systems exhibit sensitivity to hydrothermal interactions with seawater; whereas the Sm-Nd system appears essentially undisturbed by the minimal alteration experienced by the rocks drilled at Site U1415. The 87Sr/86Sr isotopic compositions of olivine gabbros (Mg# 0.81-0.89) range from 0.702536-0.703950 (±0.000008). Higher 87Sr/86Sr ratios are strongly correlated with percentage of hydrous minerals, and are higher in samples with a greater modal abundance of olivine. These rocks have somewhat higher 87Sr/86Sr ratios than upper plutonic rocks from the Northern Escarpment at Hess Deep (Kirchner and Gillis, 2012), although their percentage of hydrous phases is apparently similar. The d18O in these rocks ranges from 0.23‰ to 4.65‰ (±0.67); troctolites have systematically lower d18O than the gabbro and gabbronorites

  11. Sr-Nd isotopes and mineralogy as tracers of continental erosion and sediment transport to the Red Sea and the Gulf of Aden during the last 20,000 years

    NASA Astrophysics Data System (ADS)

    Rojas, V. P.; Meynadier, L.; Bassinot, F. C.; Christophe, C.; Valet, J. P.

    2014-12-01

    During the transition from the last glacial maximum to the Holocene, production and transport of matter into the southern part of Red Sea and Gulf of Aden were sensitive to changes in monsoon winds, rain intensity and ITCZ position. We studied two marine cores on each side of the Bab-el-Mandeb strait in order to compare the open ocean and a more isolated basin at the Eastern limit of the Arabic peninsula. Erosion and matter transfer from the continent have been documented by different approaches, which include radiogenic isotopes and mineralogy of bulk samples and clay fraction. The Sr-Nd fingerprint of detrital sediments is an effective tool for discriminating between sediment sources. Mineralogical composition also depends on lithology of the source area and can provide insight on the environmental conditions at the time of deposition. ɛNd and 87Sr/86Sr from the detrital fraction in both cores show large changes linked to the Glacial-Interglacial transition, following the foraminifera δ18O data. The isotopic values evolved towards a lower volcanic contribution from the last glaciation to the Holocene with a more pronounced change in the Gulf of Aden and more volcanic values for the Red Sea. The sediment mineralogy includes quartz, feldspar, muscovite, biotite, amphibole and pyroxene. Clay mineralogy is dominated by smectite and lesser amounts of illite and palygorskite. Correlation of percentage of smectite and Nd-Sr isotope composition agrees with a volcanic origin of smectite and shows a 2-pole mixture of sediment sources. The first end member is characterized by a large amount of smectite, positive values of ɛNd and a low 87Sr/86Sr ratio and was identified as Afar volcanic rocks. The second one with more negative values of ɛNd and a higher 87Sr/86Sr ratio is enriched in illite and palygorskite and was defined as originating from the Central Arabian region. Changes in sediment composition during the Glacial-Interglacial transition denote a variation in the

  12. Petrology and geochemistry of Cenozoic intra-plate basalts in east-central China: Constraints on recycling of an oceanic slab in the source region

    NASA Astrophysics Data System (ADS)

    Li, Yan-Qing; Ma, Chang-Qian; Robinson, Paul T.

    2016-10-01

    Cenozoic mafic rocks in Jiangsu and Anhui Provinces, east-central China are chiefly basanites and alkali olivine basalts with subordinate tholeiites, which were erupted in three stages; Paleogene, Neogene and Quaternary. The rocks become increasingly alkaline as they become younger. On a primitive mantle-normalized multi-element plot, these lavas exhibit typical OIB-like trace element patterns, including enrichment in most incompatible elements (LILE and HFSE) and negative K and Pb anomalies. The compositions of the mafic rocks indicate that they were derived from a mantle source mainly containing clinopyroxene and garnet, most probably a mixture of pyroxenite/eclogite and peridotite. A mineral equilibrium projection shows that all the mafic magmas were produced at pressures of 3-4 GPa, implying an asthenospheric origin. Their positive Ba and Sr anomalies and relatively high 87Sr/86Sr ratios suggest derivation from an EM1-type mantle source. However, poor correlations between 87Sr/86Sr and 143Nd/144Nd indicate an isotopically heterogeneous source for the magmas, including DMM, EM1 and EM2, representing mantle peridotite, recycled ancient oceanic crust and seafloor sedimentary rocks, respectively. Variable correlations between 87Sr/86Sr and 143Nd/144Nd ratios, CaO-MgO contents and Eu/Eu* and Ce/Ce* anomalies with rock type imply that marine sediments (plus variable amounts of oceanic crust) and peridotites were the dominant source lithologies of the basanites, whereas recycled oceanic crust (pyroxenite/eclogite) was the main source of the weakly alkaline basalts. This hypothesis is supported by seismic tomographic images of the mantle beneath the region, which show the presence of a stagnant subducted slab in the mantle transition zone. Thus, we propose a petrological model in which a hybrid magma column originated from the mantle transition zone and assimilated some of the overlying peridotite during upwelling, to become the parental magmas of these mafic rocks

  13. Nutrient Sourcing of Ten Plant Species in the Southwest U.S. using Strontium Isotopes: Effects of Rooting Depth, Bedrock Type, and Landscape Age

    NASA Astrophysics Data System (ADS)

    Reynolds, A. C.; Quade, J.; Betancourt, J. L.

    2007-12-01

    For decades, researchers have been examining chronosequences in Hawaii to quantify mineral weathering rates and tropical plant nutrient pools. Within El Malpais National Park, New Mexico, well-dated basalt flows allow for comparison of the Hawaiian data to a semi-arid ecosystem. We measured 87Sr/86Sr ratios in cellulose and bedrock to gauge tree, shrub, & grass (Pinus ponderosa, Pinus edulis, Juniperus monosperma, Juniperus scopulorum, Populus tremuloides, Chrysothamus nauseosus, Fallugia paradoxa, Rhus trilobata, Bouteloua gracilis, and Xanthoparmelia lineola (Berry) Hale) dependence on atmospheric dust as a nutrient source. Sampling sites varied by bedrock type (limestone, sandstone, granite, cinder and basalt) and by age (Quaternary to Precambrian) providing a wide and discrete range of 87Sr/86Sr ratios. Thus, we can pinpoint the roles landscape age (3 ka to greater than 200 ka) and bedrock recalcitrance play in mineral weathering versus eolian dust influence. This study suggests that dust dominates the nutrient cycle on younger landscapes (3 ka), shows a mixture of mineral weathering-dust inputs by 9 ka, and is rock-dominated by 120 ka. Rates of soil nutrient depletion vary in older, non-basalt landscapes (>250 ka), depending on the type the parent bedrock. For example, landscapes on Precambrian gneiss and Paleozoic limestone still show significant mineral contributions while the quartz-rich, carbonate-cemented Zuni Sandstone is almost completely eolian-dominated. Cellulose 87Sr/86Sr variation by plant species at a single site allows us to monitor plant rooting depths and interspecies competition for vital nutrients. Within semiarid ecosystems, nutrient concentrations exhibit both vertical and lateral heterogeneity. The reasons for this variation include vertical and lateral heterogeneity in soil moisture and foliar trapping of nutrient-rich dust followed by incorporation of the throughfall into the underlying soil. This study shows that throughfall does play a

  14. Sources of continental crust: neodymium isotope evidence from the sierra nevada and peninsular ranges.

    PubMed

    Depaolo, D J

    1980-08-01

    Granitic rocks from batholiths of the Sierra Nevada and Peninsular Ranges exhibit initial (143)Nd/(144)Nd ratios that vary over a large range and correlate with (87)Sr/(86)Sr ratios. The data suggest that the batholiths represent mixtures of materials derived from (i) chemically depleted mantle identical to the source of island arcs and (ii) old continental crust, probably sediments or metasediments with a provenance age of approximately 1.6 x 10(9) years. These conclusions are consistent with a model for continental growth whereby new crustal additions are repeatedly extracted from the same limited volume of the upper mantle, which has consequently become depleted in elements that are enriched in the crust. There is little evidence that hydrothermally altered, subducted oceanic crust is a primary source of the magmas. PMID:17821189

  15. Sources of continental crust: neodymium isotope evidence from the Sierra Nevada and Peninsular ranges

    SciTech Connect

    DePaolo, D.J.

    1980-08-08

    Granitic rocks from batholiths of the Sierra Nevada and Peninsular Ranges exhibit initial /sup 143/Nd//sup 144/Nd ratios that vary over a large range and correlate with /sup 87/Sr//sup 86/Sr ratios. The data suggest that the batholiths represent mixtures of materials derived from (i) chemically depleted mantle identical to the source of island arcs and (ii) old continental crust, probably sediments or metasediments with a provenance age of approx. 1.6 x 10/sup 9/ years. These conclusions are consistent with a model for continental growth whereby new crustal additions are repeatedly extracted from the same limited volume of the upper mantle, which has consequently become depleted in elements that are enriched in the crust. There is little evidence that hydrothermally altered, subducted oceanic crust is a primary source of the magmas.

  16. Hydrogeochemistry of the northern Barbados accretionary complex transect: Ocean Drilling Project leg 110

    SciTech Connect

    Gieskes, J.M. ); Vrolijk, P. ); Blanc, G. )

    1990-06-10

    Detailed studies of the major element geochemistry, oxygen and hydrogen isotope ratios of pore fluids, and the {sup 87}Sr/{sup 86}Sr ratio of dissolved strontium have made it possible to unravel physical and chemical processes that affect the pore fluid chemistry in a transect of drill holes across the northern Barbados accretionary complex. These processes include (1) alteration of volcanic ash buried in the Pleisticene-Pliocene sediment column; (2) alteration of underlying basalts of layer 2 of the oceanic crust; (3) movement of fluids from deep in the accretionary complex along fault zones (particularly the decollement) and minor permeable layers; these fluids from deeper in the complex are characterized by low chloride concentrations and increased {sup {delta}18}O(H{sub 2}O) values, presumably as a result of dehydration of smectite interlayers; and (4) mixing processes involving the migrating fluids cause incongruities in the geochemical anomalies of these fluids.

  17. 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.

  18. Use of strontium isotopes to constrain the timing and mode of dolomitization of upper Cenozoic sediments in a core from San Salvador, Bahamas

    USGS Publications Warehouse

    Swart, Peter K.; Ruiz, Joaquin; Holmes, Charles W.

    1985-01-01

    The 87Sr/86Sr ratios and the activity ratios of 234U/238U and 230Th/238U have been measured in dolomites from a 168-m-deep core taken on the island of San Salvador, Bahamas. These data suggest two periods of dolomitization. The first episode dolomitized Miocene age sediments during the latest Miocene, and the second dolomitized the Pliocene portion of the core and was still active as recently as 150 ka. The late timing of the second episode argues against penecontemporaneous models of dolomitization for the Pliocene sediments. Instead, dolomitization is favored either as a result of mixing-zone development during the large Pleistocene sea-level changes or by movement of seawater through the platform.

  19. Uranium from German Nuclear Power Projects of the 1940s— A Nuclear Forensic Investigation

    PubMed Central

    Mayer, Klaus; Wallenius, Maria; Lützenkirchen, Klaus; Horta, Joan; Nicholl, Adrian; Rasmussen, Gert; van Belle, Pieter; Varga, Zsolt; Buda, Razvan; Erdmann, Nicole; Kratz, Jens-Volker; Trautmann, Norbert; Fifield, L Keith; Tims, Stephen G; Fröhlich, Michaela B; Steier, Peter

    2015-01-01

    Here we present a nuclear forensic study of uranium from German nuclear projects which used different geometries of metallic uranium fuel.3b,d, 4 Through measurement of the 230Th/234U ratio, we could determine that the material had been produced in the period from 1940 to 1943. To determine the geographical origin of the uranium, the rare-earth-element content and the 87Sr/86Sr ratio were measured. The results provide evidence that the uranium was mined in the Czech Republic. Trace amounts of 236U and 239Pu were detected at the level of their natural abundance, which indicates that the uranium fuel was not exposed to any major neutron fluence. PMID:26501922

  20. Redox heterogeneity in mid-ocean ridge basalts as a function of mantle source.

    PubMed

    Cottrell, Elizabeth; Kelley, Katherine A

    2013-06-14

    The oxidation state of Earth's upper mantle both influences and records mantle evolution, but systematic fine-scale variations in upper mantle oxidation state have not previously been recognized in mantle-derived lavas from mid-ocean ridges. Through a global survey of mid-ocean ridge basalt glasses, we show that mantle oxidation state varies systematically as a function of mantle source composition. Negative correlations between Fe(3+)/ΣFe ratios and indices of mantle enrichment--such as (87)Sr/(86)Sr, (208)Pb/(204)Pb, Ba/La, and Nb/Zr ratios--reveal that enriched mantle is more reduced than depleted mantle. Because carbon may act to simultaneously reduce iron and generate melts that share geochemical traits with our reduced samples, we propose that carbon creates magmas at ridges that are reduced and enriched.

  1. Origin of Paleozoic volcanics, northern Sierra Nevada, California: trace element and isotopic evidence

    SciTech Connect

    Hannah, J.L.; Crock, J.G.; Goldberg, S.A.

    1985-01-01

    Oceanic arc settings for Devonian and Permian volcanic sequences in the northern Sierra Nevada are suggested by: 1) abundant andesites and dacites; 2) the overwhelming predominance of submarine pyroclastic and epiclastic rocks; 3) localized vent facies; 4) absence of phenocrystic K-feldspar, hornblende, or biotite. Abundances of relatively immobile rare earth elements (REE), Ti, Y, Zr, and Nb, are typical of island arc tholeiites. Whole rock delta/sup 18/O values of 9.2 to 13.1 per thousand reflect low-temperature alteration. Relict quartz and augite phenocrysts, however, have retained original igneous isotopic signatures, yielding average delta/sup 18/O values of 8.2 and 6.0 per thousand, respectively. These low values preclude significant crustal contamination during magma ascent. Initial /sup 87/Sr//sup 86/Sr ratios for unaltered relict augite from Devonian andesite average 0.7082; initial ratios for augite from the Permian volcanics average 0.7045, suggesting a more primitive (back-arc.) magma source. Relatively high initial ratios from the Devonian volcanics require contamination of the magma by older, high Rb/Sr material. The contaminant is most likely a slab-derived component, as crustal assimilation or alteration processes would also increase oxygen isotope ratios. Whole rock initial /sup 87/Sr//sup 86/Sr and La/Yb ratios increase systematically through the Devonian sequence. These variations, which are not readily attributed to alteration, may reflect increasing contribution of subducted sedimentary material during arc maturation and accretionary prism growth.

  2. 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

  3. 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

  4. Was Late Cretaceous Magmatism in the Northern Rocky Mountains Really Arc-Related?

    NASA Astrophysics Data System (ADS)

    Farmer, G.

    2011-12-01

    Calc-alkaline, Cretaceous magmatism affected much of the northern Rocky Mountain region in the western U.S. and is generally interpreted as continental arc magmatism despite the fact that it occurred as far east into the continental interior as the Late Cretaceous (75 Ma to 78 Ma) Sliderock Mountain volcanoplutonic complex in south-central Montana. Magmatism may have migrated so far inboard as a response to shallowing of the dip angle of underthrust oceanic lithosphere, but the exact sources, tectonic setting and trigger mechanisms for the Late Cretaceous igneous activity remain unclear. In this study, new trace element and Nd and Sr isotopic data, combined with existing age and major element data (duBray et al., 1998, USGS Prof. Paper 1602), from the most mafic lavas present at the Sliderock Mountain Volcano were used to further define the source regions of the Late Cretaceous magmatism. The most mafic lava flows are high K (~2-3 wt. % K2O), low Ti (< 1 wt. % TiO2), low Ni (< 20 ppm) basaltic andesites. Major element oxide contents for these rocks are only weakly correlated with increasing wt. % SiO2 on conventional Harker diagrams. All of the rocks are characterized by high LILE/HFSE ratios and high Pb contents (17-20 ppm), as expected for arc-related magmatism. The rocks also have high (La/Yb)N (7-20) but show decreasing (Dy/Yb)N with increasing wt.% SiO2, suggesting a cryptic role for amphibole fractionation during evolution of their parental magmas. Initial ɛNd values range from -19 to -29 but do not covary with rock bulk composition and as a result are unlikely to represent the result of interaction with local Archean continental crust. Initial 87Sr/86Sr, in contrast, vary over a restricted range from 0.7045 to 0.7065. The lowest 87Sr/86Sr correspond to samples with the highest Sr/Y (120-190). The low ɛNd values for the basaltic andesites suggest that if these volcanic rocks were ultimately derived from ultramafic mantle sources, melting must have occurred

  5. Geochronology and geochemistry of the Triassic bimodal volcanic rocks and coeval A-type granites of the Olzit area, Middle Mongolia: Implications for the tectonic evolution of Mongol-Okhotsk Ocean

    NASA Astrophysics Data System (ADS)

    Zhu, Mingshuai; Zhang, Fochin; Miao, Laicheng; Baatar, Munkhtsengel; Anaad, Chimedtseren; Yang, Shunhu; Li, Xingbo

    2016-05-01

    The Olzit volcanism in Middle Mongolia comprises a bimodal suite of basalts and peralkaline rhyolites adjacent to the Main Mongolia Lineament. The basalts are characterized by enrichment in LILE and LREE, and depletion in HFSE with typical Sr-Nd isotopic signatures (εNd(t) = -2.50 to -0.38 and (87Sr/86Sr)i = 0.7058-0.7063), indicating they were likely derived from partial melting of an enriched lithospheric mantle, modified by subducted slab-derived fluids. The rhyolites show a close affinity to A-type granites with enrichment in LILE and LREE, and depletion in Nb, Ta and Ti. They also show a significant negative Eu anomaly, and have εNd(t) values ranging from 0.50 to 1.38 and initial 87Sr/86Sr ratios ranging from 0.7022 to 0.7200, suggesting the rhyolites stem from partial melting of crustal rocks rather than fractional crystallization of the basaltic melt. The rhyolite porphyry yields a SHRIMP zircon U-Pb age of 207 ± 2 Ma (MSWD = 1.42), indicating the bimodal volcanic suite formed in the Late Triassic. The miarolitic per-alkaline granite and biotite-bearing granite, which are associated with the bimodal volcanic rocks, show typical A-type granitic geochemical affinity with εNd(t) = 0.89-0.91 and (87Sr/86Sr)i = 0.7021-0.7043, indicating they are likely generated by partial melting of crustal rocks similar to the rhyolitic end-member of bimodal suite. The miarolitic per-alkaline granite and biotite-bearing granite yielded SHRIMP zircon U-Pb ages of 209 ± 2 Ma (MSWD = 0.91) and 213 ± 3 Ma (MSWD = 1.65) respectively, which are nearly coeval with the age of the bimodal volcanic suites. In view of the new geochemical and chronological data in this study, we suggest the Olzit Late Triassic bimodal volcanic rocks together with the coeval A-type granites represent a back-arc basin extensional environment, which probably related to the roll-back of Mongol-Okhotsk oceanic plate during the southward subduction under the Central Mongolia microcontinent.

  6. Tracing and Apportioning Sources of Uranium to the Hanford Reach of the Columbia River Using Uranium Isotopes

    NASA Astrophysics Data System (ADS)

    Christensen, J. N.; Dresel, P. E.; Conrad, M. E.; Patton, G. W.; Depaolo, D. J.

    2004-12-01

    The U.S. Department of Energy's Hanford Site is situated along an unimpounded portion of the Columbia River, the highest discharge volume river west of the continental divide. Decades of nuclear related activities have left significant local contamination (e.g. nitrate, U, tritium, Cr6+, 99Tc) in the vadose zone and groundwater within the site. Some of this contamination has reached the Columbia River, and there remains the potential for further contaminant migration to the river. We collected and analyzed samples of Columbia River water for U and Sr isotopes in coordination with the ongoing sampling and monitoring of the river. The U and Sr isotopic data allow us to evaluate sources of U (e.g. natural background, Hanford related, agricultural runoff) and their relative contributions to the river's U budget. The data also provide constraints on the flux of contaminant U from the Hanford Site to the river. We analyzed two sample traverses across the Columbia, one near the Vernita Bridge, upstream from Hanford Site contamination, and a second about 5 km downstream of the Hanford Site. An island divides the downstream traverse into western (main channel) and eastern portions. Filtered (0.45 micron) water samples were analyzed for U isotopic composition (including 236U, one marker of spent U fuel) and U concentration, as well as 87Sr/86Sr and Sr concentration. The samples from the upstream traverse had no detectible 236U (236U/238U < 2x10-8), one marker of spent U fuel, natural 238U/235U, uniform (234U/238U, 87Sr/86Sr, U and Sr concentrations. In contrast, the downstream traverse showed variation in all of these parameters. Concentrations of U are 0.5 ppb to 1.2 ppb and are all well below the EPA MCL of 30 ppb for drinking water. In the western channel, measured 236U/238U is 3.4x10-5 to < 2x10-8, with a co-variation in 238U/235U toward enriched ratios. This correlation is consistent with the U isotopic compositions of a groundwater sample from the environs of a former

  7. Stable and radiogenic isotopic analysis of aquifer systems, Atlantic Rim, Carbon County, Wyoming: Implications for production of coalbed natural gas

    NASA Astrophysics Data System (ADS)

    McLaughlin, J. Fred

    Coalbed natural gas (CBNG) production requires the extraction of considerable volumes of water from target formations. This process can dynamically alter local aquifers and affect the larger hydrologic systems of a producing area. An analytical method that provides immediate, cost-effective quantitative information on both resource (methane) and habitat (coalbed aquifer) would help to optimize gas production. This study used a combination of field measurements, water chemistry analysis, and isotopic analysis, both stable (delta13C DIC, deltaO, deltaD) and radiometric (87Sr/ 86Sr), to analyze and characterize the CBNG aquifers and hydrogeologic systems of Wyoming's Atlantic Rim. Waters were sampled and analyzed from streams, springs, and CBNG wells across the Atlantic Rim. Samples were first grouped on the basis of geologic location, and then additionally defined by isotopic and water chemistry analysis into Mesaverde Group springs, Lewis Shale springs, Steele Shale springs, Sand Hill springs, enriched delta 13CDIC springs, methane springs, and subsurface samples (monitoring and CBNG wells). Two distinct water chemistry types are evident in Atlantic Rim samples, Ca-Mg-SO4-type and Na-HCO3-type waters. Atlantic Rim samples also had distinct radiogenic isotopic signatures. Stream water sourced from the Sierra Madre and waters associated with the Mesaverde Group have the highest 87Sr/86Sr ratios, whereas spring samples from the Lewis Shale have the lowest 87Sr/ 86Sr. delta13CDIC, which is enriched by bacterial methanogenesis, was used to identify coalbed waters from other natural waters. Positive delta13CDIC identified spring waters that originated from Mesaverde coalbed aquifers, including methane springs. Strongly positive delta13CDIC of Atlantic Rim CBNG samples identified those coalbed aquifers that are hydraulically isolated, whereas lower delta13CDIC identified wells within open aquifer systems and wells with inefficient casing. This study demonstrated that delta

  8. Hf sbnd Nd sbnd Sr isotopes and incompatible element abundances in island arcs: implications for magma origins and crust-mantle evolution

    NASA Astrophysics Data System (ADS)

    White, William M.; Patchett, Jonathan

    1984-02-01

    We present Hf, Nd and Sr isotopic data and abundances of K, Rb, Cs, Ba, Sr, Hf and REE for 32 samples from seven intra-oceanic island arcs. Samples from the Marianas, Izu, Aleutian and New Britain arcs have tightly grouped 176Hf/ 177Hf˜ 0.28320, 143Nd/ 144Nd˜ 0.51303 and 87Sr/ 86Sr˜ 0.7035 close to, but distinct from, mid-ocean ridge basalts (MORB) for 143Nd/ 144Nd and 87Sr/ 86Sr . In contrast, samples from the Sunda, Banda and Lesser Antilles arcs are much more variable towards lower 176Hf/ 177Hf and 143Nd/ 144Nd , and higher 87Sr/ 86Sr . Isotopically, island arcs on the whole are closely similar to ocean islands. Some commonly-occurring features of the trace element geochemistry of island arcs are apparent in our data: alkali and alkaline-earth elements, particularly Cs, have high abundance relative to LREE compared to oceanic basalts; negative Ce anomalies occur in six out of seven arcs. However, Hf does not appear underabundant relative to REE. The isotopic data require a continental component in all island arcs, in addition to probable mantle and oceanic crust contributions, even for the arcs with isotope ratios close to MORB. In the absence of continental crust, we can best explain this component by subducted pelagic sediment in the arc magma source region. The involvement of sediments in all arcs implies that there is an inherent recycling of older continent to island arcs, and potentially to new continent, of at least 1%. Conservative calculations show that the upper subducted slab (basalt + sediment) passes beyond the arc magma genesis zone and enters the deep mantle with a minimum of 500-1000 ppm K, and corresponding amounts of other incompatible elements. If this material is not completely homogenized with the mantle and later becomes part of the source of ocean island magmas, then the ocean island—island arc isotopic similarity is a result of their similar mix of source materials—mantle peridotite with trace element signatures from oceanic crust

  9. Uranium and Strontium Isotopic Study of the Hydrology of the Alluvial Aquifer at the Rifle Former U Mine Tailings Site, Colorado

    NASA Astrophysics Data System (ADS)

    Christensen, J. N.; Shiel, A. E.; Conrad, M. E.; Williams, K. H.; Dong, W.; Tokunaga, T. K.; Wan, J.; Long, P. E.; Hubbard, S. S.

    2014-12-01

    The Rifle Site consists of a floodplain along the Colorado River that was remediated through the removal of surface material underlying former uranium-vanadium mill tailings. The semi-arid (precip. = ~30 cm/year) catchment for the site has an area of ~1km2. The Rifle Site provides an excellent field laboratory for the study of the fluxes of water and carbon from the vadose zone to groundwater (LBNL SFA2.0, http://esd.lbl.gov/research/projects/sssfa2/). A network of monitoring wells, particularly a set instrumented in the vadose zone, provide the opportunity to closely sample groundwater and vadose zone porewater both in space and time. In order to better understand the spatial and temporal variation of vadose zone interaction with groundwater within the Rifle floodplain and provide constraints for a Rifle hydrological model, we have analyzed the Sr isotopic compositions, 234U/238U activity ratios, and d238U of groundwater, vadose zone porewater (sampled through depth-distributed lysimeters) and surface water including the Colorado River. Significant contrasts in 87Sr/86Sr and 234U/238U allow the identification of different sources contributing to Rifle groundwater, while d238U provides an additional tracer and insights into redox processes. Vadose zone porewater is characterized by high 87Sr/86Sr and Sr concentrations and falls at one end of a mixing line with Rifle groundwater, while upgradient groundwater with lower 87Sr/86Sr and Sr concentrations falls at the other end. A mixing model using vadose zone porewater and upgradient groundwater as endmembers suggests that the contribution of vertical recharge through the floodplain increases to ~20% systematically across the floodplain towards the Colorado River. An exception to this pattern is a well located 150m from the river with recent high U concentrations (>300 ppb) and U and Sr isotopic compositions consistent with a 38% vadose zone contribution. U and Sr isotopes show that an irrigation-return ditch that cuts

  10. Elemental and Sr Nd isotopic systematics of the early Mesozoic volcanic sequence in southern Jiangxi Province, South China: petrogenesis and tectonic implications

    NASA Astrophysics Data System (ADS)

    Wang, Yuejun; Fan, Weiming; Peng, Touping; Guo, Feng

    2005-02-01

    Elemental and Sr Nd isotopic results are presented for the early Mesozoic volcanic sequence (~172 Ma) in southern Jiangxi Province, South China. The sequence is voluminously composed of ~45% subalkaline basaltic rocks (group 1), <5% high-mg andesite dacites (group 2) and ~50% rhyolites (group 3). The group 1 rocks are characterized by (La/Yb)cn = 3.8 7.2, Eu/Eu* = 0.65 1.15, Nb/La = 0.64 0.99, 87Sr/86Sr(t) = 0.70602~0.70822 and ɛNd(t) = -1.63 to +0.11, similar to those of an EMII-like source. The group 2 rocks have mg=0.42~0.60, SiO2=60.24~66.71%, MgO=2.65~ 5.54%, Ni=24~102 ppm and Cr=84~266 ppm, classified as high-mg andesitic rocks. These rocks are more enriched in LILEs and LREE with more significant negative Eu anomaly (0.63~0.79), are more depleted in HFSEs with Nb/La ratios of 0.40 0.56 and have lower ɛNd(t) (-9.44 to -7.78) and higher 87Sr/86Sr(t) (0.70985~0.71016), in comparison with the group 1 rocks. They most likely originated from metasomatised veins in the lithospheric mantle. The origination of the group 1 and group 2 magma suggests the development of a peridotite-plus-vein lithospheric mantle during early Mesozoic era beneath the interior of the Cathaysian block. The group 3 rhyolites are characterized by high SiO2 (72.75~77.97%), Zr (99~290 ppm), Hf (3.9~9.7 ppm) and Ga/Al (2.76~3.87) and significant Nb Ta, Ba Sr and P Ti depletions. These rhyolites exhibit Sr Nd isotopic compositions (87Sr/86Sr(t) = 0.70962~0.71104, ɛNd(t) = -4.63 to -5.80) similar to the contemporaneous Zhaibei and Pitou A-type granites in the area. Such characteristics suggest that they might be derived from the underplating basaltic magma contaminated by crustal materials. Therefore, an early Mesozoic rifting model in response to intracontinental lithospheric extension is proposed to account for the early Mesozoic volcanism in southern Jiangxi Province, South China.

  11. Tracking seasonal subglacial drainage evolution of alpine glaciers using radiogenic Nd and Sr isotope systematics: Lemon Creek Glacier, Alaska

    NASA Astrophysics Data System (ADS)

    Clinger, A. E.; Aciego, S.; Stevenson, E. I.; Arendt, C. A.

    2014-12-01

    The transport pathways of water beneath a glacier are subject to change as melt seasons progress due to variability in the balance between basal water pressure and water flux. Subglacial hydrology has been well studied, but the understanding of spatial distribution is less well constrained. Whereas radiogenic isotopic tracers have been traditionally used as proxies to track spatial variability and weathering rates in fluvial and riverine systems, these techniques have yet to be applied extensively to the subglacial environment and may help resolve ambiguity in subglacial hydrology. Research has shown the 143Nd/144Nd values can reflect variation in source provenance processes due to variations in the age of the continental crust. Correlating the 143Nd/144Nd with other radiogenic isotope systematics such as strontium (87Sr/86Sr) provides important constraints on the role of congruent and incongruent weathering processes. Our study presents the application of Nd and Sr systematics using isotopic ratios to the suspended load of subglacial meltwater collected over a single melt season at Lemon Creek Glacier, USA (LCG). The time-series data show an average ɛNd ~ -6.83, indicating a young bedrock (~60 MYA). Isotopic variation helps track the seasonal expansion of the subglacial meltwater channels and subsequent return to early season conditions due to the parabolic trend towards less radiogenic Nd in June and towards more radiogenic Nd beginning in mid-August. However, the high variability in July and early August may reflect a mixture of source as the channels diverge and derive sediment from differently aged lithologies. We find a poor correlation between 143Nd/144Nd and 87Sr/86Sr (R2= 0.38) along with a slight trend towards more radiogenic 87Sr/86Sr values with time ((R2= 0.49). This may indicate that, even as the residence time decreases over the melt season, the LCG subglacial system is relatively stable and that the bedrock is congruently weathered. Our study

  12. Boron, Sr, O, and H isotope geochemistry of groundwaters from Mt. Etna (Sicily) -- Hydrologic implications

    SciTech Connect

    Pennisi, M.; Leeman, W.P.; Tonarini, S.; Pennisi, A.; Nabelek, P.

    2000-03-01

    Combined B, O, H, and Sr isotopic studies of groundwaters from Mt. Etna provide new constraints on their origin and the consequences of fluid-rock interaction within this hydrologic system. Variations in {delta}{sup 18}O ({minus}9.7 to {minus}7.2%) and {delta}D ({minus}62 to {minus}23%) mainly lie along the regional meteoric water line and suggest that most waters originated as local precipitation. However, small shifts in {delta}{sup 18}O, and variable {sup 87}Sr/{sup 86}Sr (0.70355 to 0.70879) and {delta}{sup 11}B ({minus}5.2 to 25.8%) indicate that subsequent interactions occurred between the fluids and local rocks. High B/Cl ratios in all samples seemingly preclude direct involvement of seawater in the hydrologic system despite the proximity to the coast and, in some samples, elevated {sup 87}Sr/{sup 86}Sr and {delta}{sup 11}B. Two general end-member water types are recognized on the basis of their chemistry. These apparently are produced by interactions of local meteoric waters with the dominant reservoir rocks--either basaltic lavas of Etna or the underlying sediments, respectively; high {delta}{sup 11}B in the sediment-hosted end-member points to a significant marine carbonate contribution. Subsequent mixing between these or similar end-members produced a range of intermediate composition groundwaters. Certain anomalous water compositions require the presence locally of a distinct component with high B and moderate {delta}{sup 11}B (ca. 10%) but relatively low {sup 87}/Sr/{sup 86}Sr; an anthropogenic source for this component is plausible. One unusual sample has B and Sr isotopic compositions similar to the other volcanic rock-hosted waters, but anomalously high Cl content that likely reflects local magmatic outgassing near this sampling locality. In general, this study indicates that groundwater B and Sr isotopic compositions are rock-dominated; these data provide useful constraints on the origin and evolution of groundwaters.

  13. 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 tw