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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. 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.

  4. 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

  5. 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

  6. 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.

  7. 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.

  8. 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

  9. 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.

  10. 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.

  11. Correlation of onshore-offshore Oligocene through lower Miocene strata using 87Sr/ 86Sr isotopic ratios, north flank of Cape Fear Arch, North Carolina, USA

    NASA Astrophysics Data System (ADS)

    Harris, W. B.; Mendrick, S.; Fullagar, P. D.

    2000-07-01

    Cores from onshore and offshore of the Onslow block reveal at least three depositional sequences above the Eocene Castle Hayne Limestone and below the Miocene Pungo River Formation. Through use of 87Sr/ 86Sr ratios and their resultant dates, these sequences are correlated from onshore to offshore, thus clarifying the geologic history of the inner continental shelf of North Carolina. The oldest depositional sequence consists of calcareous quartz sand and sandy, pelecypod-mold grainstone updip and yellowish gray, very fine to fine calcareous quartz sand with minor clay and silt downdip. Most of the carbonate in the downdip part of the sequence consists of foraminifers, ostracods, echinoid spines and other small allochems. Eight hand-picked foraminiferal samples, including two replicate analyses, from this sequence selected from two onshore cores and one offshore core yield 87Sr/ 86Sr ratios from 0.707901 to 0.708006 equivalent to LOWESS (Locally Weighted Regression Scatterplot Smoother) dates ranging from 29.2 to 32.0 Ma. This indicates this sequence is Rupelian (early Oligocene) in age and assignable to either the TA4.4 or TA4.5 global coastal onlap cycle. The youngest sequence consists of oyster-bearing quartz sand and laterally equivalent clay with mollusks onshore and very fine to fine calcareous quartz sand offshore. Twelve foraminiferal and one ostracod sample, including five replicate analyses, from three cores on the inner shelf of Onslow Bay yield 87Sr/ 86Sr ratios from 0.708332 to 0.708386 equivalent to LOWESS dates ranging from 21.1 to 22.2 Ma. This indicates the sequence is Aquitanian (early Miocene) in age and assignable to the TB1.4 global coastal onlap cycle. Although Chattian (late Oligocene) sequences are recognized onshore in outcrop and core and are projected to continue into Onslow Bay, no cores provided Sr samples for analysis interpreted to be late Oligocene in age.

  12. 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.

  13. Using otoliths from a non-migratory fish (Slimy sculpin - Cottus cognatus) to evaluate temporal and spatial variability in 87Sr/86Sr ratios of river waters from a large and remote watershed in southwest AK, USA - the Nushagak River

    NASA Astrophysics Data System (ADS)

    Brennan, S.; Fernandez, D. P.; Zimmerman, C.; Cerling, T. E.; Wooller, M. J.

    2013-12-01

    Heterogeneity in 87Sr/86Sr ratios of river-dissolved strontium (Sr) across geologically diverse watersheds and landscapes is a useful tool for investigating provenance, connectivity and movement patterns of various materials and organisms. Evaluating temporal variation across watersheds at different spatial scales is expensive and difficult, especially in remote areas, but is necessary to accurately interpret Sr isotopic data. We used the time-keeping properties inherent to otoliths, the ever-growing aragonitic auditory structure of teleost fish, from non-migratory Slimy sculpin (Cottus cognatus) to evaluate seasonal and inter-annual temporal variability in 87Sr/86Sr ratios of river waters throughout a large watershed in remote Alaska, USA - the Nushagak River. Using laser ablation multi-collector inductively coupled plasma mass-spectrometry, 87Sr/86Sr ratios were measured from core to edge of otoliths from Slimy sculpin (n = 20) ranging in age from 3 to 6 years old captured at various sites within the Nushagak River watershed. Generalized additive models (GAMs) of 87Sr/86Sr profiles indicate that the majority of individuals (n = 14) exhibit no significant isotopic variation (p > 0.05) from core to edge of otoliths, though some did exhibit significant isotopic variation (n = 6, p << 0.05). In some instances, sculpin caught at the same site showed characteristically different 87Sr/86Sr profiles, which we interpret as variations in the micro-movements and life histories of these fish versus time-dependent changes in the 87Sr/86Sr ratio of water at a particular site. This study illustrates the use of otoliths from non-migratory fish to evaluate seasonal and inter-annual variability in 87Sr/86Sr ratios of river-dissolved Sr at multiple spatial scales within a watershed.

  14. 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., Jr.

    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.

  15. 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. PMID:27374544

  16. 87Sr/86Sr-ratios, foraminiferal data and sedimentology of the Latest Miocene - Pliocene cyclic carbonates of La Désirade (Guadeloupe, France)

    NASA Astrophysics Data System (ADS)

    Weber*, P. J. N.; Baumgartner-Mora*, C.; Baumgartner*, P. O.

    2012-04-01

    La Désirade is a small island located east of Grande Terre and Basse Terre, the main islands of the Guadeloupe Archipelago in the Lesser Antilles Arc. La Désirade is an "forearc outer high" located immediately west of the trench where Atlantic crust is presently subducted under the Caribbean Plate. The "Limestone Table" (LT) of La Désirade has been considered as a Plio-Quaternary reefal deposit. However, the prominent feature of this <140 m thick formation is its rhythmic bedding of alternating marly/tuffaceous/dolomitic, and winnowed bioclastic carbonate layers. To the west of the island the "detrital offshore limestones" represent alternating offshore marls, tuffs and channelled mass flow deposits, that accumulated below wave base beneath a steep fore-reef slope. They document the mobilisation of carbonate material on an adjacent platform by storms and their gravitational emplacement. The provenance of both the reefal carbonate debris and the tuffaceous components must be to the west, i. e. Marie Galante and Grande Terre. We have studied the biochronology of both benthic and planktonic foraminifera and measured 87Sr/86Sr ratios of selected biogenic shells such as aragonitic gastropods, corals, echinoderms and foraminifera. Recrystallisation and preservation has been controlled by SEM, cathodoluminescence, carbon/oxygen isotopes and XRF to avoid diagenetically altered samples. Planktonic foraminifera of the "detrital offshore limestones" give a latest Miocene/early Pliocene age (lower zone N19), while 87Sr/86Sr -ratios cluster in the latest Miocene-earliest Pliocene, depending on the calibration applied. For the LT 87Sr/86Sr ratios from the base of the section cluster in the earliest Pliocene, while the top gives a late middle to late Pliocene age. These ages constrain the Neogene vertical tectonic movements of the island. We have also dated Pleistocene terraces and fringing reefs that are in an unconformable contact along paleocliffs with the Mio

  17. 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

  18. 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.

  19. 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.

  20. 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

  1. 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

  2. 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.

  3. 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.

  4. 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.

  5. 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

  6. 87Sr/86Sr sourcing of ponderosa pine used in Anasazi great house construction at Chaco Canyon, New Mexico

    USGS Publications Warehouse

    Reynolds, Amanda C.; Betancourt, Julio L.; Quade, Jay; Patchett, P. Jonathan; Dean, Jeffery S.; Stein, John

    2005-01-01

    Previous analysis of 87Sr/86Sr ratios shows that 10th through 12th century Chaco Canyon was provisioned with plant materials that came from more than 75 km away. This includes (1) corn (Zea mays) grown on the eastern flanks of the Chuska Mountains and floodplain of the San Juan River to the west and north, and (2) spruce (Picea sp.) and fir (Abies sp.) beams from the crest of the Chuska and San Mateo Mountains to the west and south. Here, we extend 87Sr/86Sr analysis to ponderosa pine (Pinus ponderosa) prevalent in the architectural timber at three of the Chacoan great houses (Pueblo Bonito, Chetro Ketl, Pueblo del Arroyo). Like the architectural spruce and fir, much of the ponderosa matches the 87Sr/86Sr ratios of living trees in the Chuska Mountains. Many of the architectural ponderosa, however, have similar ratios to living trees in the La Plata and San Juan Mountains to the north and Lobo Mesa/Hosta Butte to the south. There are no systematic patterns in spruce/fir or ponderosa provenance by great house or time, suggesting the use of stockpiles from a few preferred sources. The multiple and distant sources for food and timber, now based on hundreds of isotopic values from modern and archeological samples, confirm conventional wisdom about the geographic scope of the larger Chacoan system. The complexity of this procurement warns against simple generalizations based on just one species, a single class of botanical artifact, or a few isotopic values.

  7. 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.

  8. 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.

  9. 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.

  10. 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.

  11. 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.

  12. High-resolution late Maastrichtian early Danian oceanic 87Sr/86Sr record: Implications for Cretaceous-Tertiary boundary events

    NASA Astrophysics Data System (ADS)

    Vonhof, H. B.; Smit, J.

    1997-04-01

    A high-resolution late Maastrichtian early Danian seawater 87Sr/86Sr reference curve is constructed from two Cretaceous-Tertiary boundary (K-T boundary) sections: Bidart (France) and El Kef (Tunisia). The 87Sr/86Sr curve shows maxima at 0.3 0.4 Ma before the K-T boundary and at the K-T boundary. The first maximum could mark the onset of a major outflow of the Deccan Traps. The second maximum, a rapid 0.000 06 87Sr/86Sr, shift, extends from ˜3 4 m below to ˜1 m above the K-T boundary. This profile probably results from diagenetic smoothing of an originally sharp K-T boundary 87Sr/86Sr anomaly, rather than from a gradual process. The sharp shift could result from (1) the vaporization of the Chicxulub target rocks, (2) global wildfires, and (3) acid-rain leaching of soils and sialic surface rocks. Of these three possibilities, only Sr release by soil leaching combined with increased rainfall associated with the K-T event appears to be sufficiently large to produce the observed K-T 87Sr/86Sr anomaly.

  13. 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

  14. 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

  15. 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

  16. The 87Sr/86Sr and 143Nd/144Nd disequilibrium between Polynesian hot spot lavas and the clinopyroxenes they host: Evidence complementing isotopic disequilibrium in melt inclusions

    NASA Astrophysics Data System (ADS)

    Jackson, Matthew G.; Hart, Stanley R.; Shimizu, Nobumichi; Blusztajn, Jerzy S.

    2009-03-01

    We report 87Sr/86Sr and 143Nd/144Nd data on clinopyroxenes recovered from 10 ocean island lavas from three different hot spots (Samoa, Society, and Cook-Austral island chains). The clinopyroxenes recovered from eight of the 10 lavas analyzed in this study exhibit 87Sr/86Sr disequilibrium with respect to the host lava. The 87Sr/86Sr ratios in clinopyroxene separates are 95-3146 ppm (0.0095-0.31%) different from their respective host whole rocks. Clinopyroxenes in three lavas have 143Nd/144Nd ratios that are 70-160 ppm (0.007-0.016%) different from the host lavas. The 87Sr/86Sr and 143Nd/144Nd disequilibrium in one lava (the oldest lava considered in this study, Mangaia sample MGA-B-47) can be attributed to posteruptive radiogenic ingrowth, but the isotope disequilibrium in the other, younger lavas cannot be explained by this mechanism. In five of the lava samples, two populations of clinopyroxene were isolated (black and green, separated by color). In four out of five of these samples, the 87Sr/86Sr ratios of the two clinopyroxene populations are isotopically different from each other. In addition to 87Sr/86Sr disequilibrium, the two clinopyroxene populations in one of the lavas (Tahaa sample TAA-B-26) have 143Nd/144Nd ratios that are ˜100 ppm different from each other. Given the resilience of clinopyroxene to seawater alteration and the likelihood that the Sr and Nd isotope composition of fresh clinopyroxene separates provides a faithful record of primary magmatic compositions, the clinopyroxene-clinopyroxene isotope disequilibrium in these four lavas provides strong evidence that a mechanism other than seawater alteration has generated the observed isotopic disequilibrium. This study confirms the isotopic diversity in ocean island lavas previously observed in olivine-hosted melt inclusions. For example, the Sr isotopic variability previously observed in olivine-hosted melt inclusions is mirrored by the isotopic diversity in clinopyroxenes isolated from many of

  17. A lithology-based model for 87Sr/86Sr values of bedrock and water in the conterminous US

    NASA Astrophysics Data System (ADS)

    Bataille, C. P.; Bowen, G. J.

    2010-12-01

    Although variation in 87Sr/86Sr has been widely pursued as a tracer of provenance in environmental studies, forensics, archeology and food traceability, accurate models of the large-scale variation in environmental 87Sr/86Sr are not available. In this paper, we build upon earlier efforts to model 87Sr/86Sr in the USA bedrock by considering the effects of lithological variation on rock and surface water. For each major group of rock, we developed combined theoretical/empirical equations describing variations of 87Sr/86Sr as a function of lithology and time and fitted the parameters to a global database of rock 87Sr/86Sr (GEOROCK-Start). Marine carbonates were modeled separately based on the work of Shield and Veizer, 2002. Evaluated relative to 300 rock Sr isotope data from the USA, the new model explains 74% of the Sr isotope variance and closely matches the real value with a standard deviation of 0.0018. In comparison, the earlier model describes 34% of the variance in the same dataset with a standard deviation 0.0039. We developed a second model to predict the Sr isotopic composition of river waters based on bedrock, but also considering differential weathering rates and strontium concentration (GEOROCK_start) for different kind of rock. The results demonstrate that the water model is necessary to account for the effect of carbonates and/or differential weathering rate of Sr-rich rock in many watersheds. In addition, it illustrates a strong linear correlation between the water model and surface water in most of the watersheds. However, in order to accurately predict surface water values, it is also necessary to account for surficial geology and local deposition phenomenon.

  18. 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.

  19. 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.

  20. 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.

  1. 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

  2. 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.

  3. 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

  4. 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).

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

    USGS Publications Warehouse

    Saltzman, M. R.; Edwards, C. T.; Leslie, S. A.; Dwyer, 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

  6. 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

  7. 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

  8. 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

  9. 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).

  10. 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.

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

    PubMed

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

    2015-03-15

    The lack of a geographical identification protocol for olive oils can lead to fraud and health risks. As some works call for Sr isotopes for the geographical identification of agri-food products, this study focus on the feasibility of extracting Sr from olive oils for isotopic measurements by TIMS. In fact, existing protocols for purification of Sr are unsuitable for lipid matrix. The defined protocol is applied to samples of PDO Nîmes olive oil. The accuracy of the extraction procedure is tested against isotopic standards. The values obtained are in conformity with NIST certified values. This consistency demonstrates that no modification of (87)Sr/(86)Sr ratio is brought about by this protocol. Consequently, the method is preliminary used on PDO Nîmes and Moroccan oils to evaluate the feasibility of a discriminant Sr signature on the two geographical products. This study provides promising results for the geographical discrimination and identification of PDO olive oils. PMID:25308645

  12. 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

  13. 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.

  14. 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

  15. 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

  16. Seasonal Variability of Riverine Geochemistry (87Sr/86Sr, δ13CDIC, δ44/40Ca, and major ions) in Permafrost Watersheds on the North Slope of Alaska

    NASA Astrophysics Data System (ADS)

    Lehn, G. O.; Jacobson, A. D.; Douglas, T. A.; McClelland, J. W.; Khosh, M. S.; Barker, A. J.

    2014-12-01

    Global climate models predict amplified warming at high latitudes, where permafrost soils have historically acted as a carbon sink. As warming occurs, the seasonally thawed active layer will propagate downward into previously frozen mineral-rich soil, releasing carbon and introducing unique chemical weathering signatures into rivers. We use variations in the 87Sr/86Sr, δ13CDIC, δ44/40Ca, and major ion geochemistry of rivers to track seasonal active layer dynamics. We collected water from six streams on the North Slope of Alaska between May and October, 2009 and 2010. All rivers drain continuous permafrost but three drain tussock tundra-dominated watersheds and three drain steeper bedrock catchments with minor tundra coverage. In tundra streams, elevated 87Sr/86Sr ratios, low δ13CDIC values and major ions ([Na+]+[K+]/ [Ca+2]+[Mg+2]) in spring melt runoff suggest flushing of shallow soils with relatively low carbonate content. By July, 87Sr/86Sr ratios stabilize at relatively low values and δ13CDIC at relatively higher values, indicating the active layer thawed into deeper carbonate-rich soils. In bedrock streams, elevated 87Sr/86Sr ratios correlate with high discharge. By late fall, bedrock stream 87Sr/86Sr ratios decrease steadily, consistent with increased carbonate weathering. Nearly constant δ13CDIC values and high [SO4-2] for most of the melt season imply significant sulfuric acid-carbonate weathering in bedrock streams. δ13CDIC values suggest a shift to carbonic acid-carbonate weathering in late 2010, possibly due to limited oxygen for pyrite oxidation during freezing of the active layer. δ44/40Ca values in both tundra and bedrock streams increase during the seasons, suggesting increased uptake of 40Ca by plants. δ44/40Ca values of rivers are at least 0.1-0.2‰ higher than their watershed soils, rocks and sediments, suggesting significant plant uptake. Our findings show how seasonal changes in mineral weathering have potential for tracking active

  17. 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.

  18. 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

  19. 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

  20. 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.

  1. 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.

  2. 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

  3. 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.

  4. 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

  5. 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.

  6. Decoupling of unpolluted temperate forests from rock nutrient sources revealed by natural 87Sr/86Sr and 84Sr tracer addition

    PubMed Central

    Kennedy, Martin J.; Hedin, Lars O.; Derry, Louis A.

    2002-01-01

    An experimental tracer addition of 84Sr to an unpolluted temperate forest site in southern Chile, as well as the natural variation of 87Sr/86Sr within plants and soils, indicates that mechanisms in shallow soil organic horizons are of key importance for retaining and recycling atmospheric cation inputs at scales of decades or less. The dominant tree species Nothofagus nitida feeds nearly exclusively (>90%) on cations of atmospheric origin, despite strong variations in tree size and location in the forest landscape. Our results illustrate that (i) unpolluted temperate forests can become nutritionally decoupled from deeper weathering processes, virtually functioning as atmospherically fed ecosystems, and (ii) base cation turnover times are considerably more rapid than previously recognized in the plant available pool of soil. These results challenge the prevalent paradigm that plants largely feed on rock-derived cations and have important implications for understanding sensitivity of forests to air pollution. PMID:12119394

  7. 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

  8. 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

  9. 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.

  10. A box model of the Late Miocene Mediterranean Sea: Implications from combined 87Sr/86Sr and salinity data

    NASA Astrophysics Data System (ADS)

    Topper, R. P. M.; Flecker, R.; Meijer, P. Th.; Wortel, M. J. R.

    2011-09-01

    Under certain conditions the strontium isotope ratio in the water of a semi-enclosed basin is known to be sensitive to the relative size of ocean water inflow and river input. Combining Sr-isotope ratios measured in Mediterranean Late Miocene successions with data on past salinity, one can derive quantitative information on the Mediterranean hydrological budget at times before and during the Messinian Salinity Crisis (MSC). Previous studies obtained this hydrological budget by inverting the salinity and strontium data with steady state solutions to the conservation equations of salt, strontium and water. Here, we develop a box model with a time-dependent set of equations to investigate the coeval evolution of salinity and Sr ratios under different water budgets, gateway restrictions and riverine Sr characteristics. Model results are compared with the salinity and strontium ratio data from the Mediterranean. With a present-day water budget, strontium ratios in the Mediterranean never reach the observed Messinian values regardless of gateway restriction and water budget. However, a model with tripled river input, as inferred for the Late Miocene, is able to reproduce the Sr ratios observed. The onset of the MSC can be explained with a simple restriction of the gateway(s) between the Mediterranean and Atlantic. Lower Evaporite gypsum formed in a basin with less outflow to the Atlantic than modeled in previous studies because of the large Late Miocene river input. Evaporite thicknesses predicted by our model and consistent with the Messinian Sr ratios are on the low end of the thickness range inferred from seismics.

  11. 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.

  12. 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.

  13. 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

  14. 87Sr/86Sr anomalies in Late Cretaceous-Early Tertiary strata of the Cauvery basin, south India: Constraints on nature and rate of environmental changes across K-T boundary

    NASA Astrophysics Data System (ADS)

    Ramkumar, Mu; Stüben, Doris; Berner, Zsolt; Schneider, Jens

    2010-02-01

    The Ariyalur-Pondicherry sub-basin of the Cauvery basin comprises a near complete stratigraphic record of Upper Cretaceous-Lower Tertiary periods. Earlier studies have documented variations of clay mineral assemblages, change in microtexture of siliciclasts and many geochemical and stable isotopic anomalies far below the Cretaceous-Tertiary boundary (KTB) in these strata. This paper documents the occurrences of two positive 87Sr/86Sr anomalies preceding K-T boundary in this basin and discusses plausible causes. Analysis of trace elemental and stable isotopic profiles, sedimentation history, petrography and mineralogy of the rocks reveal that while both the anomalies may be due to increased detrital influx caused by sea level and climatic changes, the second anomaly might have been influenced by Deccan volcanism which in turn predated KTB. Record of such anomalies preceding K-T boundary supports the view of multi-causal step-wise extinction of biota across KTB.

  15. 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.

  16. 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.

  17. The Sr-87/Sr-86 ratio as a powerful tool in forensic investigations

    NASA Astrophysics Data System (ADS)

    de Muynck, D.; Boyen, S.; Delporte, S.; de Winne, J.; Vanhaecke, F.; Degryse, P.

    2009-04-01

    As a result of the decay of the naturally occurring and long-lived radionuclide Rb-87 into Sr-87, the Sr-87/Sr-86 ratio of a geological material displays geographical variations according to the chemical/mineralogical composition of that material and its geological age. As most part of the strontium, ingested into the human body via the food, is transported to the skeletal tissue, the Sr-87/Sr-86 ratio of an individual's skeletal tissue is a reflection of the geological area in which that individual resided at the moment the skeletal tissue under investigation was formed. Distinct tissues in the human body display a different growth and Sr renewal rate, and hence reflect the place of residence in a distinct period of life (tooth enamel: childhood - tooth dentine and bone tissue: last years of life - nails: last months of life - hair: last weeks of life). Following these considerations, it was investigated if Sr isotope ratio analysis of human hair, nails, bone and dental tissue can be successfully applied in the context of forensic research. Hair, nails, bone and dental tissue of several unidentified persons, currently being investigated by the Disaster Victim Identification unit of the Belgian Federal Police, were available for research. After acid digestion and isolation of the Sr fraction using an extraction chromatographic separation, the Sr-87/Sr-86 ratio of these tissues was determined via multicollector ICP-MS. It was shown that Sr isotope ratio data match traceable facts or information obtained via independent evidence concerning the victim, e.g., by pinpointing his/her area of residence. In this way, it was demonstrated that Sr isotope ratio analysis delivers information that strengthens or weakens arguments concerning a person's identity.

  18. 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

  19. 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

  20. 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

  1. 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.

  2. 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

  3. A comparative study of results obtained in magnetotelluric deep soundings in Villarrica active volcano zone (Chile) with gravity investigations, distribution of earthquake foci, heat flow empirical relationships, isotopic geochemistry 87Sr/ 86Sr and SB systematics

    NASA Astrophysics Data System (ADS)

    Muñoz, M.; Fournier, H.; Mamani, M.; Febrer, J.; Borzotta, E.; Maidana, A.

    seismic activity from a depth of 100 km down to 160 km. Kaufman and Keller and Levi and Lysak empirical relationships between heat flow and thickness of the lithosphere are somewhat consistent when the parameters of the model structure are assumed. The strontium isotope ratios are indicative of minimal crustal contamination of mantle-derived magmas, thus allowing a relatively thin crust under the area. Furthermore, the SB index of partial melting of mantle peridotite may suggest the contribution of uprising material from the deep asthenosphere through fractures extending to depth.

  4. 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.

  5. 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

  6. 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

  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. 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.

  12. 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.

  13. 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

  14. 147,146Sm-143,142Nd, 176Lu-176Hf, and 87Rb-87Sr systematics in the angrites: Implications for chronology and processes on the angrite parent body

    NASA Astrophysics Data System (ADS)

    Sanborn, Matthew E.; Carlson, Richard W.; Wadhwa, Meenakshi

    2015-12-01

    Angrites are a group of basaltic achondrites with distinctive mineralogic and geochemical characteristics that have the potential to provide insights into processes occurring on planetesimals in the early Solar System. These achondrites have been used as anchors linking the relative age information obtained from short-lived, extinct chronometers (e.g., Al-Mg, Hf-W, and Mn-Cr) with absolute chronometers (e.g., U-Pb). Angrites provide excellent examples of early differentiation processes, such as core formation and silicate differentiation, on protoplanetary bodies. The significant increase in the number of known angrite samples in recent years has offered the opportunity to compare several short- and long-lived isotopic systems in samples with different petrogenetic histories that formed on the same parent body. To this end, the 147Sm-143Nd, 146Sm-142Nd, 176Lu-176Hf, and 87Rb-87Sr isotope systematics have been investigated in a suite of plutonic, coarse-grained (NWA 4590, NWA 4801, and NWA 2999) and quenched, fine-grained (D'Orbigny) angrites. The coupled 147,146Sm-143,142Nd systematics indicate possible isotopic disturbances in two angrites (D'Orbigny and NWA 2999) resulting from post-crystallization processes. The internal 146Sm-142Nd isochrons of two coarse-grained angrites (NWA 4590 and NWA 4801) provide an updated best estimate of the initial Solar System 146Sm/144Sm ratio (i.e., at 4568 Ma) of 0.0084 ± 0.0003. The 176Lu-176Hf isotope systematics in these angrites do not provide evidence of a previously proposed intense irradiation event in the early Solar System. The internal 176Lu-176Hf isochrons for the NWA 4590 and D'Orbigny angrites provide an estimate for the Solar System initial 176Hf/177Hf ratio of 0.279775 ± 0.000031 (2σ) that agrees within uncertainty with the value of average chondrites reported by Bouvier et al. (2008). Finally, the calculated initial 87Sr/86Sr ratios based on the measured Sr-isotopic composition of plagioclase in these angrites

  15. Degenerate Fermi Gas of {sup 87}Sr

    SciTech Connect

    DeSalvo, B. J.; Yan, M.; Mickelson, P. G.; Martinez de Escobar, Y. N.; Killian, T. C.

    2010-07-16

    We report quantum degeneracy in a gas of ultracold fermionic {sup 87}Sr atoms. By evaporatively cooling a mixture of spin states in an optical dipole trap for 10.5 s, we obtain samples well into the degenerate regime with T/T{sub F}=0.26{sub -0.06}{sup +0.05}. The main signature of degeneracy is a change in the momentum distribution as measured by time-of-flight imaging, and we also observe a decrease in evaporation efficiency below T/T{sub F{approx}}0.5.

  16. 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

  17. Precise determination of strontium isotope ratios by TIMS to authenticate tomato geographical origin.

    PubMed

    Trincherini, P R; Baffi, C; Barbero, P; Pizzoglio, E; Spalla, S

    2014-02-15

    Thermal Ionisation Mass Spectrometry (TIMS) was applied to discriminate a total of 118 tomato samples (berries, "passata", tinned tomatoes, sauce, double and triple concentrate) coming from two different countries. The TIMS technique gave significantly different results for the (87)Sr/(86)Sr ratios and δ‰ values between Chinese and Italian tomato samples, irrespective of the treatment type. This technique proved to be a "robust" method, suitable for a precise discrimination of the two geographical origins. TIMS was able, within the Italian samples, to discriminate different geographical production areas, by virtue of different (87)Sr/(86)Sr ratios and δ‰ values. This technique could be employed in the field of food safety and quality, as a profitable tool for authenticating tomato geographical origin. PMID:24128488

  18. 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}.

  19. 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.

  20. An observed link between lithophile compositions and degassing of volatiles (He, Ar, CO2) in MORBs with implications for Re volatility and the mantle C/Nb ratio

    NASA Astrophysics Data System (ADS)

    Burnard, Pete; Reisberg, Laurie; Colin, Aurélia

    2014-06-01

    There are systematic variations between relative noble gas abundances and lithophile tracers such as 87Sr/86Sr, εNd and La/Sm in a suite of basaltic glasses from the South East Indian Ridge (SEIR). 4He/40Ar* (where 40Ar* is 40Ar corrected for atmospheric contamination) correlates positively with 87Sr/86Sr and La/Sm but anticorrelates with εNd. The large range in 4He/40Ar* observed in the glasses is due to fractionation during magmatic degassing caused by the very different solubilities of He and Ar in silicate liquids, whereas 87Sr/86Sr, εNd, La/Sm, etc. are insensitive to magmatic processes but rather reflect mantle heterogeneity. Thus, there is a curious situation in this suite of basalts where tracers of mantle heterogeneity (87Sr/86Sr, εNd, La/Sm, etc.) correlate with a tracer of magmatic volatile processes (4He/40Ar*). Here, we propose that “enriched” mantle (with high La/Sm and 87Sr/86Sr, low εNd) also has a higher C concentration than “depleted” mantle. Magmas derived from enriched mantle will therefore have higher initial C concentrations, leading to a greater fraction of CO2 degassed and thus a higher 4He/40Ar* ratio on eruption. Simple solubility-determined fractional degassing models show that the range in 4He/40Ar* observed in SEIR basaltic glasses can be generated if the mantle C concentration varies by a factor of 2 over the length of the ridge, consistent with independent estimates of C concentration heterogeneity in the MORB mantle. The correlations between lithophile tracers and 4He/40Ar* can be reproduced by mixing between a depleted endmember with 87Sr/86Sr = 0.70275, εNd = 8.2 and [C] = 12 ppm and an enriched endmember with 87Sr/86Sr = 0.70360, εNd = 5 and [C] = 24 ppm, followed by degassing. The proposed degassing model allows us to estimate the initial C concentration (i.e. prior to degassing) of each SEIR basalt (for which Sr or Nd isotopes are available); using independent Nb concentration data (Mahoney et al., 2002), we show

  1. Precessional control of Sr ratios in marginal basins during the Messinian Salinity Crisis?

    NASA Astrophysics Data System (ADS)

    Topper, R. P. M.; Lugli, S.; Manzi, V.; Roveri, M.; Meijer, P. Th.

    2014-05-01

    on 87Sr/86Sr data of the Primary Lower Gypsum (PLG) deposits in the Vena del Gesso basin—a marginal basin of the Mediterranean during the Messinian Salinity Crisis—a correlation between 87Sr/86Sr values and precessional forcing has recently been proposed but not yet confirmed. In this study, a box model is set up to represent the Miocene Mediterranean deep basin and a connected marginal basin. Measurements of 87Sr/86Sr in the Vena del Gesso and estimated salinity extrema are used to constrain model results. In an extensive analysis with this model, we assess whether coeval 87Sr/86Sr and salinity fluctuations could have been forced by precession-driven changes in the fresh water budget. A comprehensive set of the controlling parameters is examined to assess the conditions under which precession-driven 87Sr/86Sr variations occur and to determine the most likely setting for PLG formation. Model results show that precession-driven 87Sr/86Sr and salinity fluctuations in marginal basins are produced in settings within a large range of marginal basin sizes, riverine strontium characteristics, amplitudes of precessional fresh water budget variation, and average fresh water budgets of both the marginal and deep basin. PLG deposition most likely occurred when the Atlantic-Mediterranean connection was restricted, and the average fresh water budget in the Mediterranean was significantly less negative than at present day. Considering the large range of settings in which salinities and 87Sr/86Sr fluctuate on a precessional timescale, 87Sr/86Sr variations are expected to be a common feature in PLG deposits in marginal basins of the Mediterranean.

  2. 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.

  3. 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.

  4. The absolute frequency of the 87Sr optical clock transition

    NASA Astrophysics Data System (ADS)

    Campbell, Gretchen K.; Ludlow, Andrew D.; Blatt, Sebastian; Thomsen, Jan W.; Martin, Michael J.; de Miranda, Marcio H. G.; Zelevinsky, Tanya; Boyd, Martin M.; Ye, Jun; Diddams, Scott A.; Heavner, Thomas P.; Parker, Thomas E.; Jefferts, Steven R.

    2008-10-01

    The absolute frequency of the 1S0-3P0 clock transition of 87Sr has been measured to be 429 228 004 229 873.65 (37) Hz using lattice-confined atoms, where the fractional uncertainty of 8.6 × 10-16 represents one of the most accurate measurements of an atomic transition frequency to date. After a detailed study of systematic effects, which reduced the total systematic uncertainty of the Sr lattice clock to 1.5 × 10-16, the clock frequency is measured against a hydrogen maser which is simultaneously calibrated to the US primary frequency standard, the NIST Cs fountain clock, NIST-F1. The comparison is made possible using a femtosecond laser based optical frequency comb to phase coherently connect the optical and microwave spectral regions and by a 3.5 km fibre transfer scheme to compare the remotely located clock signals.

  5. 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.

  6. 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.

  7. Bose-Einstein condensation of {sup 86}Sr

    SciTech Connect

    Stellmer, Simon; Grimm, Rudolf; Tey, Meng Khoon; Schreck, Florian

    2010-10-15

    We report on the attainment of Bose-Einstein condensation of {sup 86}Sr. This isotope has a scattering length of about +800a{sub 0} and thus suffers from fast three-body losses. To avoid detrimental atom loss, evaporative cooling is performed at low densities around 3x10{sup 12} cm{sup -3} in a large volume optical dipole trap. We obtain almost pure condensates of 5x10{sup 3} atoms.

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

    PubMed

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

    2016-04-15

    The concentrations of dissolved strontium (Sr) and isotope ratios ((87)Sr/(86)Sr) in rainwater, river water, and water from forest soil are measured to investigate the contributions of these sources to a river during base flow conditions in the relatively pristine South Qinling Mountains, China. Dissolved Sr concentrations and (87)Sr/(86)Sr ratios vary significantly between different water types (p < 0.01) suggesting that it is suitable for differentiating sources. Dissolved Sr is also positively correlated with most ions and a range of physicochemical parameters (p < 0.01 and p < 0.05 respectively) in water samples including Ca(2+), Mg(2+), EC, and TDS (p < 0.001) indicating their similarities in the drivers of biogeochemical processes and common origins. The correlations between Sr isotopes and Ca/Na, Ca/K, and 1000/Sr ratios suggest that three end-members of atmospheric inputs, carbonate and silicate weathering control the Sr water chemistry in the river water. Using the three-source mixing model, atmospheric inputs, carbonate, and silicate weathering contribute 74%, 20%, and 6% respectively to the dissolved Sr in the river water. This research has provided new insights into the contribution of sources of Sr to a river system in a mountainous catchment. PMID:26900970

  9. 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

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

    NASA Technical Reports Server (NTRS)

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

    1991-01-01

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

  11. 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

  12. 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.

  13. Standardless determination of Nd and Sr isotope ratios in geological samples using LA-MC-ICP-MS with a low-oxide molecular yield interface setup

    NASA Astrophysics Data System (ADS)

    Kimura, J.; Chang, Q.; Takahashi, T.; Kawabata, H.

    2013-12-01

    We investigated an appropriate instrumental setup for a laser-ablation multiple-collector inductively coupled plasma mass spectrometer (LA-MC-ICP-MS) and found that a reduced oxide setting allowed accurate and precise analyses of Sr and Nd isotope ratios in geological samples with concomitant interfering elements (Kr and Rb on Sr and Sm on Nd). We used an Aridus II solution-excimer laser dual-intake system. The ICP interface used normal sample and skimmer cones with torch shield switched-OFF and an additional large interface rotary pump. The setting accomplished reduced oxide levels NdO+/Nd+ <0.01%, without significant sacrifice of the instrumental sensitivity (c.a. 70%). Oxide molecular ions for the lighter elements were negligible and accurate internal mass bias corrections were achieved for Sr, Sm, and Nd using isotopic ratios derived from thermal ionization mass spectrometry measurements. However, elemental fractionation between Rb and Sr and Nd and Sm still exists due perhaps to elemental fractionation in the ICP preventing standardless determination of parent-daughter ratios. For Sr isotope measurement, a new analytical protocol was developed for correcting Kr baseline-induced biases. Residual analytical biases of 84Sr/86Sr and 87Sr/86Sr were observed after applying on-peak background subtractions and mass-fractionation corrections using internal normalization. The residual biases occurred only for samples analysed with LA and not for solution analyses using Aridus II with the same instrumental setup. We concluded that this was due to suppression and enhancement of the Kr baseline by loading of the LA sample aerosols and by the introduction of Kr from the samples, respectively. We found that both the 84Sr/86Sr and 87Sr/86Sr isotope ratios were affected proportionally by the baseline biases of the LA analyses of an isotopically homogeneous anorthite plagioclase, and similar result were seen in theoretical calculations. A theoretical bias correction for the 87

  14. 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.

  15. Bose-Einstein condensation of {sup 88}Sr through sympathetic cooling with {sup 87}Sr

    SciTech Connect

    Mickelson, P. G.; Martinez de Escobar, Y. N.; Yan, M.; DeSalvo, B. J.; Killian, T. C.

    2010-05-15

    We report Bose-Einstein condensation of {sup 88}Sr, which has a small, negative s-wave scattering length (a{sub 88}=-2a{sub 0}). We overcome the poor evaporative cooling characteristics of this isotope by sympathetic cooling with {sup 87}Sr atoms. {sup 87}Sr is effective in this role despite the fact that it is a fermion because of the large ground-state degeneracy arising from a nuclear spin of I=9/2, which reduces the impact of Pauli blocking of collisions. We observe a limited number of atoms in the condensate (N{sub max{approx_equal}}10{sup 4}) that is consistent with the value of a{sub 88} and the optical dipole trap parameters.

  16. 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.

  17. 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.

  18. Evaluation of variation in ( m_p/m_e) from the frequency difference between the 15N2+ and 87Sr transitions

    NASA Astrophysics Data System (ADS)

    Kajita, Masatoshi

    2016-07-01

    The uncertainty of the 87Sr1 S0-3 P0 transition frequency (429 THz) has been reduced to the level of 10^{-18}. Also, the 15N2+ Q(0) vibrational transition frequency is expected to be measured with an uncertainty of 10^{-17} , and the v = 0-7 transition frequency (422 THz) is close to the 87Sr transition frequency. In this paper, we propose a test for the variation in the proton-to-electron mass ratio μ via precise measurement of the difference (f_d=7 THz) between these transition frequencies. By measuring f_d within the uncertainty of 10^{-16}, a variation in μ of 4 × 10^{-18} can be detected. The 15N2+ v =0 -7 Q(0) transition frequency is free from Zeeman and electric quadrupole shifts. The dc Stark coefficient is about 0.2 mHz/(V/cm)2, and the measurement of f_d with an uncertainty lower than 10^{-16} appears to be attainable using molecular ions in a string crystal. The 15N2+ transition frequency is observed via the two-photon excitation of a laser with a wavelength of 1422 nm (laser A). Another laser with a wavelength of 1396 nm (laser B) is used as a 87Sr clock laser after frequency doubling. The frequency difference between lasers A and B (3.5 THz) should be measured using a frequency comb. Lasers A and B can be transferred to another laboratory via an optical fiber. Therefore, a sensitive test of the variation in μ can be performed in cooperation between two distant laboratories.

  19. 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.

  20. {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.

  1. 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.

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

    USGS Publications Warehouse

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

    1991-01-01

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

  3. Towards the next decades of precision and accuracy in a 87Sr optical lattice clock

    NASA Astrophysics Data System (ADS)

    Martin, Michael; Lin, Yige; Swallows, Matthew; Bishof, Michael; Blatt, Sebastian; Benko, Craig; Chen, Licheng; Hirokawa, Takako; Rey, Ana Maria; Ye, Jun

    2011-05-01

    Optical lattice clocks based on ensembles of neutral atoms have the potential to operate at the highest levels of stability due to the parallel interrogation of many atoms. However, the control of systematic shifts in these systems is correspondingly difficult due to potential collisional atomic interactions. By tightly confining samples of ultracold fermionic 87Sr atoms in a two-dimensional optical lattice, as opposed to the conventional one-dimensional geometry, we increase the collisional interaction energy to be the largest relevant energy scale, thus entering the strongly interacting regime of clock operation. We show both theoretically and experimentally that this increase in interaction energy results in a paradoxical decrease in the collisional shift, reducing this key systematic to the 10-17 level. We also present work towards next- generation ultrastable lasers to attain quantum-limited clock operation, potentially enhancing clock precision by an order of magnitude. This work was supported by a grant from the ARO with funding from the DARPA OLE program, NIST, NSF, and AFOSR.

  4. Systematic Study of the ^87Sr Clock Transition in an Optical Lattice

    NASA Astrophysics Data System (ADS)

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

    2006-05-01

    The ^1S0-^3P0 transition in ^87Sr is studied for the realization of an optical atomic clock, using μK atoms in a magic wavelength optical lattice [1]. The probe laser frequency is measured with an octave-spanning fs comb, which is referenced to a hydrogen maser (directly calibrated by the NIST primary Cs fountain clock) allowing high precision evaluation of potential systematic frequency shifts . By varying the lattice wavelength and trapping depth we find that the magic wavelength for the clock transition is 813.418(10) with a clock sensitivity to lattice deviations of ˜2 mHz/MHz for lattice intensities of 10 kW/cm^2. To explore the effect of atomic collisions on the clock frequency we varied the atomic density by a factor of 50 and did not find any shifts at the 3 x10-14 level. Dependence of the clock transition on magnetic fields has been examined as the hyperfine interaction (I = 9/2), which provides the small transition moment for the doubly forbidden clock transition, also results in a differential g factor of the ^3P0 and ^1S0 levels. We will report the latest results of this optical clock system. [1] A.D. Ludlow et al., Phys Rev Lett 96, 033003 (2006).

  5. Miocene seawater 187Os/ 188Os ratios inferred from metalliferous carbonates

    NASA Astrophysics Data System (ADS)

    Reusch, Douglas N.; Ravizza, Greg; Maasch, Kirk A.; Wright, James D.

    1998-07-01

    Seawater 187Os/ 188Os ratios for the Middle Miocene were reconstructed by measuring the 187Os/ 188Os ratios of metalliferous carbonates from the Pacific (DSDP 598) and Atlantic (DSDP 521) oceans. Atlantic and Pacific 187Os/ 188Os measurements are nearly indistinguishable and are consistent with previously published Os isotope records from Pacific cores. The Atlantic data reported here provide the first direct evidence that the long-term sedimentary 187Os/ 188Os record reflects whole-ocean changes in the Os isotopic composition of seawater. The Pacific and the Atlantic Os measurements confirm a long-term 0.01/Myr increase in marine 187Os/ 188Os ratios that began no later than 16 Ma. The beginning of the Os isotopic increase coincided with a decrease in the rate of increase of marine 87Sr/ 86Sr ratios at 16 Ma. A large increase of 1‰ in benthic foraminiferal δ18O values, interpreted to reflect global cooling and ice sheet growth, began approximately 1 million years later at 14.8 Ma, and the long-term shift toward lower bulk carbonate δ13C values began more than 2 Myr later around 13.6 Ma. The post-16 Ma increase in marine 187Os/ 188Os ratios was most likely forced by weathering of radiogenic materials, either old sediments or sialic crust with a sedimentary protolith. We consider two possible Miocene-specific geologic events that can account for both this increase in marine 187Os/ 188Os ratios and also nearly constant 87Sr/ 86Sr ratios: (1) the first glacial erosion of sediment-covered cratons in the Northern Hemisphere; (2) the exhumation of the Australian passive margin-New Guinea arc system. The latter event offers a mechanism, via enhanced availability of soluble Ca and Mg silicates in the arc terrane, for the maintenance of assumed low CO 2 levels after 15 Ma. The temporal resolution (three samples/Myr) of the 187Os/ 188Os record from Site 598, for which a stable isotope stratigraphy was also constructed, is significantly higher than that of previously

  6. 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.

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

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

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

  8. 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.

  9. 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.

  10. Identifying weathering sources and processes in an outlet glacier of the Greenland Ice Sheet using Ca and Sr isotope ratios

    NASA Astrophysics Data System (ADS)

    Hindshaw, Ruth S.; Rickli, Jörg; Leuthold, Julien; Wadham, Jemma; Bourdon, Bernard

    2014-11-01

    Chemical and isotope data (ε40Ca, δ44/42Ca, 87Sr/86Sr, δ18O) of river water samples were collected twice daily for 28 days in 2009 from the outlet river of Leverett Glacier, West Greenland. The water chemistry data was combined with detailed geochemical analysis and petrography of bulk rock, mineral separates and sediment samples in order to constrain the mineral weathering sources to the river. The average isotopic compositions measured in the river, with 2SD of all the values measured, were ε40Ca = +4.0 ± 1.4, δ44/42Ca = +0.60 ± 0.10‰ and 87Sr/86Sr = 0.74243 ± 0.00327. Based on changes in bulk meltwater discharge, the hydrochemical data was divided into three hydrological periods. The first period was marked by the tail-end of an outburst event and was characterised by water with decreasing suspended sediment concentrations (SSC), ion concentrations and pH. During the second hydrological period, discharge increased whilst 87Sr/86Sr decreased from 0.74550 to 0.74164. Based on binary mixing diagrams using 87Sr/86Sr with Na/Sr, Ca/Sr and ε40Ca, this is interpreted to reflect an increase in reactive mineral weathering, in particular epidote, as the water residence time decreases. The decrease in water residence time is a result of the evolution from a distributed (long water residence time) to a channelised (short water residence time) subglacial drainage network. The third hydrological period was defined as the period when overall discharge was decreasing. This hydrological period was marked by prominent diurnal cycles in discharge. During this period, significant correlations between δ44/42Ca and SSC and δ18O were observed which are suggestive of fractionation during adsorption. This study demonstrates the potential of radiogenic Ca to both identify temporally changing mineral sources in conjunction with 87Sr/86Sr values and to separate source and fractionation effects in δ44/42Ca values.

  11. Improved Frequency Measurement of a One-Dimensional Optical Lattice Clock with a Spin-Polarized Fermionic 87Sr Isotope

    NASA Astrophysics Data System (ADS)

    Takamoto, Masao; Hong, Feng-Lei; Higashi, Ryoichi; Fujii, Yasuhisa; Imae, Michito; Katori, Hidetoshi

    2006-10-01

    We demonstrate a one-dimensional optical lattice clock with a spin-polarized fermionic isotope designed to realize a collision-shift-free atomic clock with neutral atom ensembles. To reduce systematic uncertainties, we developed both Zeeman shift and vector light-shift cancellation techniques. By introducing both an H-maser and a global positioning system (GPS) carrier phase link, the absolute frequency of the 1S0(F=9/2)-{}3P0(F=9/2) clock transition of the 87Sr optical lattice clock is determined as 429,228,004,229,875(4) Hz, where the uncertainty is mainly limited by that of the frequency link. The result indicates that the Sr lattice clock will play an important role in the scope of the redefinition of the “second” by optical frequency standards.

  12. 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.

  13. 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).

  14. 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.

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

    NASA Astrophysics Data System (ADS)

    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-temporal 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.

  16. Suppression of collisional shifts via strong inter-atomic interactions in a 87Sr optical lattice clock

    NASA Astrophysics Data System (ADS)

    Martin, Michael; Swallows, Matthew; Bishof, Michael; Lin, Yige; Blatt, Sebastian; Rey, Ana Maria; Ye, Jun

    2011-05-01

    Optical lattice clocks based on ensembles of neutral atoms have the potential to operate at the highest levels of stability due to the parallel interrogation of many atoms. However, the control of systematic shifts in these systems is correspondingly difficult due to the potential of collisional shifts. Clocks based on ultracold fermionic ensembles still exhibit these density-dependent shifts due to a loss of indistinguishability during the clock excitation process, limiting clock accuracy. By tightly confining samples of ultracold fermionic 87Sr atoms in a two-dimensional optical lattice, as opposed to the conventional one-dimensional geometry, we increase the collisional interaction energy to be the largest relevant energy scale, thus entering the strongly interacting regime of clock operation. We show both theoretically and experimentally that this increase in interaction energy results in a paradoxical decrease in the collisional shift, reducing this key systematic to the 10-17 level. This work was supported by the ARO with funding from the DARPA OLE program, NIST, NSF, and AFOSR.

  17. Sr isotopic characteristics in two small watersheds draining typical silicate and carbonate rocks: implication for the studies on seawater Sr isotopic evolution

    NASA Astrophysics Data System (ADS)

    Wu, W. H.; Zheng, H. B.; Yang, J. D.

    2013-06-01

    We systematically investigated Sr isotopic characteristics of small silicate watershed - the tributary Xishui River of the Yangtze River, and small carbonate watershed - the tributary Guijiang River of the Pearl River. The results show that the Xishui River has relatively high Sr concentrations (0.468-1.70 μmol L-1 in summer and 1.30-3.17 μmol L-1 in winter, respectively) and low 87Sr/86Sr ratios (0.708686-0.709148 in summer and 0.708515-0.709305 in winter), which is similar to the characteristics of carbonate weathering. The Guijiang River has low Sr concentrations (0.124-1.098 μmol L-1) and high 87Sr/86Sr ratios (0.710558-0.724605), being characterized by silicate weathering. In the Xishui River catchment, chemical weathering rates in summer are far higher than those in winter, indicating significant influence of climate regime. However, slight differences of 87Sr/86Sr ratios between summer and winter show that influence of climate on Sr isotope is uncertainty owing to very similar Sr isotope values in silicate and carbonate bedrocks. As 87Sr/86Sr ratios in the Xishui River are lower than those in seawater, they will decrease 87Sr/86Sr ratio of seawater after transported into oceans. Previous studies also showed that some basaltic watersheds with extremely high chemical weathering rates reduced the seawater Sr isotope ratios. In other words, river catchments with high silicate weathering rates do not certainly transport highly radiogenic Sr into oceans. Therefore, it may be questionable that using the variations of seawater 87Sr/86Sr ratio to indicate the continental silicate weathering intensity. In the Guijiang River catchment, 87Sr/86Sr ratios of carbonate rocks and other sources (rainwater, domestic and industrial waste water, and agricultural fertilizer) are lower than 0.71. In comparison, some non-carbonate components, such as, sand rocks, mud rocks, shales, have relatively high Sr isotopic compositions. Moreover, granites accounted for only 5% of the

  18. 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. PMID:23909446

  19. 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.

  20. 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.

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

    USGS Publications Warehouse

    Tepley, F. J., III; 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.

  2. 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. PMID:26802358

  3. 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

  4. 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. PMID:25186083

  5. 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.

  6. Measurement of c-axis optical absorptivity of La{sub 1.87}Sr{sub 0.13}CuO{sub 4}

    SciTech Connect

    Birmingham, J.T.; Grannan, S.M.; Richards, P.L.; Henn, R.; Kircher, J.; Cardona, M.; Wittlin, A.; Duijn, V.H.M.; Menovsky, A.A.

    1996-12-31

    The authors have directly measured the c-axis optical absorptivity of a large single crystal of La{sub 1.87}Sr{sub 0.13}CuO{sub 4} between 9 and 80 cm{sup {minus}1} at 2 K using Fourier transform spectroscopy and an absorbed power technique. They see an absorptivity onset at 41 cm{sup {minus}1}, which is 2--3 cm{sup {minus}1} higher than that measured at 6 K with reflectance on the same sample, suggesting that a significant fraction of the electrons remain unpaired at 6 K. The absorption increases with frequency below the onset, increasing from 0.3% at 9 cm{sup {minus}1} to 8% at 40 cm{sup {minus}1}. The data are particularly significant at frequencies below the plasma edge, for which the reflectance is close to unity.

  7. 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.

  8. Hyperfine structure and Zeeman tuning of the A {sup 2}PI-X {sup 2}SIGMA{sup +}(0,0) band system of the odd isotopologue of strontium monofluoride {sup 87}SrF

    SciTech Connect

    Le, Anh T.; Wang Hailing; Steimle, Timothy C.

    2009-12-15

    The low-rotational lines of the A {sup 2}PI-X {sup 2}SIGMA{sup +}(0,0) band system of the odd isotopologue of strontium monofluoride, {sup 87}SrF, were recorded and analyzed. The {sup 87}Sr(I=9/2) magnetic hyperfine interaction is significant only in the |OMEGA|=1/2 spin-orbit component of the A {sup 2}PI state. Optical transitions appropriate for monitoring ultracold samples of {sup 87}SrF are identified. The determined fine-structure parameters were used to predict the anisotropic magnetic g factor, g{sub l}, for the X {sup 2}SIGMA{sup +}(v=0) state. The g factors were used to predict the magnetic tuning of the N=0 (+parity) and N=1 (-parity) levels of the X {sup 2}SIGMA{sup +}(v=0) state. A comparison to spectroscopic parameters for the {sup 88}SrF isotopologue is given.

  9. 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.

  10. 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.

  11. 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.

  12. Oxygen and strontium isotope studies of K-rich volcanic rocks from the Alban Hills, Italy

    NASA Astrophysics Data System (ADS)

    Ferrara, G.; Laurenzi, M. A.; Taylor, H. P.; Tonarini, S.; Turi, B.

    1985-09-01

    18O/ 16O and 87Sr/ 86Sr ratios and major and trace element contents were measured for 33 leucite-bearing lavas from the Alban Hills, located just south of Rome. Petrologically, this volcanic center is the least complex of all the Pleistocene to Holocene volcanoes in the Roman Comagmatic Province, and the 87Sr/ 86Sr uniformity reflects this (0.71024-0.71091). Whole-rock δ 18O = +5.6 to +9.8, but many samples were enriched in 18O by post-eruption hydration, evidenced by the good correlation between H 2O content (up to 5 wt. %) and δ 18O . Correcting for these effects, we obtain a δ 18O range of +5.6 to +7.8 for the original magmas. No other volcanic center in the Roman Province displays such uniform strontium and oxygen isotopic compositions; thus, this volcano provides special insight into the origin of the High-K Series magma end-member in Central Italy. Three groups of lavas are recognized on 87Sr/ 86Sr-1/Sr, δ 18O- 87Sr/ 86Sr , and K 2O-SiO 2 graphs; all of these groups, as well as the major caldera-forming eruption (Villa Senni Tuff), are derived from a very uniform, LIL-enriched, metasomatized source in the upper mantle. This source had δ 18O = +6.5 ± 1.0 and 87Sr/ 86Sr= 0.71030 ± 0.00010 . The δ 18O values correlate positively with 87Sr/ 86Sr , indicating minor interaction with the continental crust. Essentially all chemical and isotopic variations in the primitive (low-SiO 2, high-Ca, high-Sr) potassic lavas in Italy can be explained by mixing in the upper mantle between this Alban Hills end-member and a Low-K Series Roccamonfina-type end-member.

  13. 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

  14. 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

  15. 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

  16. 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

  17. 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.

  18. 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.

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

    PubMed

    Bastos, Murilo Q R; Souza, Sheila M F Mendonça de; Santos, Roberto V; Lima, Bárbara A F; Santos, Ricardo V; Rodrigues-Carvalho, Claudia

    2011-06-01

    This study investigated strontium isotopes in the dental enamel of 32 human skeletons from Forte Marechal Luz sambaqui (shellmound), Santa Catarina, Brazil, aiming at identifying local and non-local individuals. The archeological site presents pot sherds in the uppermost archeological layers. Dental enamel was also examined from specimens of terrestrial fauna ((87)Sr/(86)Sr = 0.71046 to 0.71273) and marine fauna ((87)Sr/(86)Sr = 0.70917). The (87)Sr/(86)Sr isotope ratio for individuals classified as locals ranged from 0. 70905 to 0. 71064 and was closer to the isotope ratio of the seawater than to the ratio of the terrestrial fauna, indicating a strong influence of marine strontium on the inhabitants of this sambaqui. The results indicate the existence of three non-local individuals ((87)Sr/(86)Sr = 0.70761 to 0.70835), buried in both the level without pottery and the layer with pottery, possibly originated from the Santa Catarina Plateau, close to the municipality of Lages, or from the Curitiba Plateau. The occurrence of a slight difference between the isotope ratios of local individuals buried in the archeological layer without pottery, when compared to those in the layer with pottery, suggests a possible change in dietary patterns between these two moments in the site's occupation. PMID:21670891

  20. 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.

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

    USGS Publications Warehouse

    Harris, W.B.; Self-Trail J.M.

    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

  2. Orphan Strontium-87 in Abyssal Peridotites: Daddy Was a Granite

    NASA Astrophysics Data System (ADS)

    Snow, Jonathan E.; Hart, Stanley R.; Dick, Henry J. B.

    1993-12-01

    The 87Sr/86Sr 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," 87Sr appears to be separated from its radioactive parent. Such observations were widely held to be analytical artifacts. Study of several occurrences of orphan 87Sr shows that the orphan component in abyssal peridotite is located in the alteration products of olivine and enstatite in the peridotite. The orphan 87Sr is most likely introduced by infiltration of low-temperature (<200^circC) 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 87Sr and other radiogenic isotopes may provide a tracer for low-temperature seawater penetrating into the oceanic crust.

  3. 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

  4. 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

  5. Gateway restriction and climatic conditions of the Mediterranean Sea during the Messinian Salinity Crisis; A box model including Sr-isotope ratios

    NASA Astrophysics Data System (ADS)

    Topper, Robin; Meijer, Paul; Flecker, Rachel; Wortel, Rinus

    2010-05-01

    Under certain conditions the ratio of two stable isotopes of strontium present in the water of a semi-enclosed basin (87Sr/86Sr) is known to be sensitive to the relative size of the inflow of ocean water and river input. Combining Sr-isotope ratios measured in Mediterranean Late Miocene successions with data on past salinity, Flecker et al. (EPSL, 203, 221-233, 2002) and Flecker and Ellam (Sed.Geol., 188-189, 189-203, 2006) were able to derive quantitative information on the Mediterranean hydrological budget at times before and during the Messinian Salinity Crisis (MSC). The authors obtained this hydrological budget by inverting the salinity and strontium data with steady-state solutions to the conservation equations of salt, strontium and water. In this study, we incorporate strontium concentration, Sr-isotope ratio and a Late Miocene water budget from Gladstone et al. (P3, 251, 254-267, 2007) in the box model from Meijer (EPSL, 248, 486-494, 2006) which quantifies the water and salt budget of the basin under specified conditions of connectivity with the Atlantic Ocean, representing tectonic restrictions of the Rifian and Betic gateways, and atmospheric fluxes, induced by climatic changes. This model will give insight in the coeval behaviour of salt and Sr-isotope ratios under changing contributions of ocean and fresh water. With respect to the model of Flecker et al. (2002) the extended model is a significant advancement as it allows for examination of the temporal evolution of salt and Sr-isotope ratio as a function of the individual hydrologic fluxes (Atlantic inflow and outflow, river input and evaporation, instead of the inflow and outflow parameters used by Flecker et al. (2002)), and the possibility of non-equilibrium states during the Late Miocene. Model evaluation is performed using the Sr-isotope ratio data set compiled by Flecker and Ellam (2006). Results from our model have implications for the timing and extent of Late Miocene Atlantic gateway

  6. 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

  7. 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.

  8. 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

  9. 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.

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. Nd- and Sr-isotopic compositions of lavas from the northern Mariana and southern Volcano arcs: implications for the origin of island arc melts

    NASA Astrophysics Data System (ADS)

    Lin, P. N.; Stern, R. J.; Morris, J.; Bloomer, S. H.

    1990-09-01

    Nd- and Sr-isotopic data are reported for lavas from 23 submarine and 3 subaerial volcanoes in the northern Mariana and southern Volcano arcs. Values of ɛNd range from +2.4 to +9.5 whereas 87Sr/86Sr ranges from 0.70319 to 0.70392; these vary systematically between and sometimes within arc segments. The Nd-and Sr-isotopic compositions fall in the field of ocean island basalt (OIB) and extend along the mantle array. Lavas from the Volcano arc, Mariana Central Island Province and the southern part of the Northern Seamount Province have ɛNd to +10 and 87Sr/86Sr=0.7032 to 0.7039. These are often slightly displaced toward higher 87Sr/86Sr at similar ɛNd. In contrast, those lavas from the northern part of the Mariana Northern Seamount Province as far north as Iwo Jima show OIB isotopic characteristics, with ɛNd and 87Sr/86Sr=0.7035 to 0.7039. Plots of 87Sr/86Sr and ɛNd versus Ba/La and (La/Yb)n support a model in which melts from the Mariana and Volcano arcs are derived by mixing of OIB-type mantle (or melts therefrom) and a metasomatized MORB-type mantle (or melts therefrom). An alternate interpretation is that anomalous trends on the plots of Nd- and Sr-isotopic composition versus incompatible-element ratios, found in some S-NSP lavas, suggest that the addition of a sedimentary component may be locally superimposed on the two-component mixing of mantle end-members.

  15. 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

  16. 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.

  17. 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, C.; Liu, Y.; Min, N.; Zong, K.; Hu, Z.; Gao, S.

    2015-12-01

    In-situ major and trace elements and Sr isotopic compositions of peridotite xenoliths carried by the Datong Quaternary alkaline basalt were analyzed. These peridotite xenoliths were classified into three groups. The type 1 peridotites preserve depleted trace element and Sr isotopic signatures and record the lowest temperature (930 - 980 °C). Clinopyroxenes in these peridotites exhibit LREE-depleted REE patterns, and have the lowest 87Sr/86Sr ratios of 0.70243 - 0.70411. The types 2 and 3 peridotites are featured by enriched trace element and Sr isotopic signatures and record a higher temperature (1003 - 1032 °C). Clinopyroxenes in the type 2 peridotite have U-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 enrichments in LILE and depletions in HFSE, and have the highest 87Sr/86Sr ratios of 0.71147 - 0.71285. The types 2 and 3 peridotites suffered latter cryptic carbonatitic metasomatism, as indicated by the decreased Ti/Eu and increased Zr/Hf and CaO/Al2O3 ratios of clinopyroxenes. The carbonatitic veinlets have generally consistent trace element patterns and Sr isotopic ratios with the calculated melts being equilibrated with the clinopyroxenes in the type 3 peridotite, and may represent the metasoamtic agent solidified in the relatively cold and shallow mantle. The negative Eu anomalies (0.37 - 0.61) and high 87Sr/86Sr ratios of the calculated melts indicate a crustal sedimentary origin. It is speculated that the REE-rich and high-87Sr/86Sr metasoamtic agent should be carbonatitic melt derived from the carbonated pelite carried by the subducted PAOP, which could have contributed to the transformation of the lithospheric mantle beneath the NCC.

  18. 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

  19. The seawater Sr isotopic evolution

    NASA Astrophysics Data System (ADS)

    Kuznetsov, A. B.; Gorokhov, I. M.; Semikhatov, M. A.; Maslov, A. V.; Krupenin, M. T.; Melnikov, N. N.

    2003-04-01

    Progress toward a reconstruction of the 87Sr/86Sr variations in Proterozoic seawater is still deficient compared to the Phanerozoic. There is no universally recognized curve, and some of its versions are in conflict. The construction of a reference curve should be based on: (1) the study of several thick carbonate-bearing successions within single paleobasin, (2) the reliable isotope dating of these successions, (3) the geochemical screening of least-altered carbonate samples, (4) a selective dissolution of samples to enrich them in primary carbonate generations. This approach was applied to study Late Proterozoic marine carbonate successions of the South Urals and East Siberia. Three comprehensive fragments of 87Sr/86Sr seawater curve were obtained: (1) the descending trend from 0.70562-0.70596 to 0.70519-0.70523 at 1050-1000 Ma, (2) the ascending trend from 0.70525-0.70535 to 0.70611-70625 at 850-750 Ma, and (3) the area of minor fluctuations from 0.70540 to 0.70610 at 680-660 Ma. The Sr- and C-isotope data for the South Urals allow us to revise the current stratigraphic correlations and impose some constraints on the age of the classic Upper Proterozoic successions of North Canada (Shaler Gr) and Svalbard (Akademikerbreen Gr): (1) the carbonate formations in middle part of the Shaler Gr appear to have been deposited after 800 Ma, (2) the rate of sedimentation of the Akademikerbreen succession was likely to be higher than it was proposed. The data from East Siberia postulate predominance of the low 87Sr/86Sr ratio during culmination stage of the Grenville orogenic cycle and decrease in this ratio in post-Grenvillian ocean. This fact markedly distinguishes the Grenville orogeny from the Pan-African orogeny which resulted in rise of seawater 87Sr/86Sr ratio up to 0.7085. The following factors were responsible for the low 87Sr/86Sr ratio in Grenvillian and post-Grenvillian oceans: a high role of mantle rocks in the exhumed orogens, a sea-level rise and partial

  20. Ancient carbonate sedimentary signature in the Hawaiian plume: Evidence from Mahukona volcano, Hawaii

    NASA Astrophysics Data System (ADS)

    Huang, Shichun; Abouchami, Wafa; Blichert-Toft, Janne; Clague, David A.; Cousens, Brian L.; Frey, Frederick A.; Humayun, Munir

    2009-08-01

    Lavas from Mahukona, a small Hawaiian volcano on the Loa trend, exhibit major and trace element abundance variations exceeding those in lavas from large Hawaiian shields, such as Mauna Loa and Mauna Kea. Mahukona lavas define three geochemically distinct groups of tholeiitic shield basalt and a transitional group of postsshield basalt. At 10% MgO the tholeiitic groups range from 9 to 12% CaO; such differences in CaO can reflect partial melts derived from garnet pyroxenite (low CaO) and peridotite (high CaO), but the negative CaO-Yb (both at 10% MgO) trend formed by Mahukona lavas is inconsistent with this explanation. Within Mahukona lavas, radiogenic Nd-Hf-Pb isotopic ratios are highly correlated with each other; however, 87Sr/86Sr is decoupled from these radiogenic isotopic ratios. Rather, 87Sr/86Sr is correlated with trace element abundance ratios involving Sr, and importantly, Mahukona lavas define a negative Rb/Sr-87Sr/86Sr trend, implying that a Sr-rich source component characterized by high 87Sr/86Sr is important in the petrogenesis of Mahukona lavas. We infer that this Sr-rich source component is recycled ancient carbonate-rich sediments. Intershield heterogeneity among Hawaiian shields also shows a negative Rb/Sr-87Sr/86Sr trend. For example, Makapuu-stage Koolau lavas have higher 87Sr/86Sr but lower Rb/Sr than Mauna Kea lavas. Consequently, we infer that a recycled ancient carbonate-rich sedimentary source component is important in the Hawaiian plume. Although most lavas from Loa and Kea trend volcanoes define distinct fields in isotopic ratios of Sr, Nd, Hf, and Pb, the majority of Mahukona lavas have isotopic ratios at the boundary between the fields defined by Loa and Kea trend lavas. However, a subgroup of Mahukona shield lavas have Kea-like isotopic and trace element signatures, an observation that can be explained by vertical heterogeneity in a bilaterally asymmetrical plume.

  1. 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.

  2. Enriched components in the Hawaiian plume: Evidence from Kahoolawe Volcano, Hawaii

    NASA Astrophysics Data System (ADS)

    Huang, Shichun; Frey, Frederick A.; Blichert-Toft, Janne; Fodor, R. V.; Bauer, Glenn R.; Xu, Guangping

    2005-11-01

    The geochemical differences between individual Hawaiian shields provide clues to the magma source components in the Hawaiian plume. Lavas from Koolau (Makapuu-stage) and Kahoolawe volcanoes define the enriched, i.e., relatively high 87Sr/86Sr and low 143Nd/144Nd, extreme for Hawaiian shield lavas. There are, however, important geochemical differences between these shields; Kahoolawe lavas lack the relatively high SiO2, low CaO, and high Sr/Nb and La/Nb that are characteristic of Makapuu-stage Koolau lavas, and they are offset from other Hawaiian shield lavas to high 87Sr/86Sr at a given 143Nd/144Nd. Consequently, a varying role for recycled plagioclase-rich gabbro is inferred, in particular, lower amounts of the low 87Sr/86Sr component in Kahoolawe lavas. Also, lavas from Loa-trend volcanoes, such as Kahoolawe, define trends ranging toward high 208Pb*/206Pb* and 87Sr/86Sr and low 143Nd/144Nd and 176Hf/177Hf. Such trends are consistent with variable amounts of recycled sediment sampled by Loa-trend volcanoes, with the largest proportion in Makapuu-stage Koolau lavas. Therefore the enriched component in the Hawaiian plume, the Koolau component, is recycled oceanic crust, which is heterogeneous because of varying proportions of sediment, basalt, and gabbro. Hawaiian shield-stage lavas range widely in 87Sr/86Sr, 143Nd/144Nd, 176Hf/177Hf, and 206Pb/204Pb, but they have similar ratios of Sr/Nd, Nd/Hf, and Hf/Pb, each varying by a factor of <3 among the Hawaiian shields. This observation has important consequences. Namely, the similar Hf/Pb ratios are inconsistent with a two-component (i.e., Kea and Koolau) mixing model for explaining the hyperbolic trend of 176Hf/177Hf versus 206Pb/204Pb defined by shield lavas. Such a model requires end-members with very different Hf/Pb (a factor of 15 to 40), but this is not observed; therefore a third component must be involved. On the basis of trends of 208Pb*/206Pb* versus 87Sr/86Sr, 143Nd/144Nd, and 176Hf/177Hf, we infer that Loa

  3. 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

  4. 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.

  5. 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.

  6. B/Nb and δ 11B systematics in the Phlegrean Volcanic District, Italy

    NASA Astrophysics Data System (ADS)

    Tonarini, S.; Leeman, W. P.; Civetta, L.; D'Antonio, M.; Ferrara, G.; Necco, A.

    2004-05-01

    Boron concentration and isotopic compositions were determined in representative products from the Phlegrean Volcanic District (PVD), which includes Campi Flegrei (CF), and the islands of Procida and Ischia. The most primitive products (from Procida and Ischia islands) are moderately enriched in B (4.6-12 ppm), whereas more evolved products of CF and Ischia Island are more enriched (21-118 ppm). The content of B is positively correlated with Nb, Zr, Th, La and, generally, with all incompatible elements. δ 11B values are generally lower and more uniform in samples from CF (-6.8 to - 10.6‰) compared with those from Procida (-3.6 to -8.5‰) and Ischia (-2.8 to -8.4‰) islands. Overall, B-enrichments relative to fluid-immobile elements of PVD are only slightly higher than those observed in mid-ocean ridge basalts and there is no significant correlation between δ 11B and B/immobile element ratios. For CF samples including the Campanian Ignimbrite (CI) and most post-CI products, δ 11B is negatively correlated with 87Sr/ 86Sr, with extreme compositions represented by evolved products of the CI (higher δ 11B, lower 87Sr/ 86Sr) and less evolved shoshonite (lower δ 11B, higher 87Sr/ 86Sr). In contrast, samples from Procida, Ischia, and pre-CI products and one young shoshonite from CF define a distinct correlation with primitive trachybasalt as the high δ 11B, low 87Sr/ 86Sr end-member, and young shoshonites as the low δ 11B, high 87Sr/ 86Sr end-member. The overall interpretation of the geochemical and isotopic data suggests three conclusions: (1) Geochemical and isotopic variations of post-CI products from CF can be explained by mixing/mingling between at least two distinct magmas, i.e. the CI and the young shoshonite (Minopoli 1). (2) The isotopic trend described by Procida trachybasalts, Ischia samples, pre-CI samples from CF and Pigna St. Nicola shoshonite is a mantle trend suggesting the involvement in their genesis of a distinct component depleted in B, with

  7. Isotopic evidence for the source of Ca and S in soil gypsum, anhydrite and calcite in the Atacama Desert, Chile

    NASA Astrophysics Data System (ADS)

    Rech, Jason A.; Quade, Jay; Hart, William S.

    The origin of pedogenic salts in the Atacama Desert has long been debated. Possible salt sources include in situ weathering at the soil site, local sources such as aerosols from the adjacent Pacific Ocean or salt-encrusted playas (salars), and extra-local atmospheric dust. To identify the origin of Ca and S in Atacama soil salts, we determined δ 34S and 87Sr/ 86Sr values of soil gypsum/anhydrite and 87Sr/ 86Sr values of soil calcite along three east-west trending transects. Our results demonstrate the strong influence of marine aerosols on soil gypsum/anhydrite development in areas where marine fog penetrates inland. Results from an east-west transect located along a breach in the Coastal Cordillera show that most soils within 90 km of the coast, and below 1300 m in elevation, are influenced by marine aerosols and that soils within 50 km, and below 800 m in elevation, receive >50% of Ca and S from marine aerosols (δ 34S values > 14‰ and 87Sr/ 86Sr values >0.7083). In areas where the Coastal Cordillera is >1200 m in elevation, however, coastal fog cannot penetrate inland and the contribution of marine aerosols to soils is greatly reduced. Most pedogenic salts from inland soils have δ 34S values between +5.0 to +8.0‰ and 87Sr/ 86Sr ratios between 0.7070 and 0.7076. These values are similar to average δ 34S and 87Sr/ 86Sr values of salts from local streams, lakes, and salars (+5.4 ±2‰ δ 34S and 0.70749 ± 0.00045 87Sr/ 86Sr) in the Andes and Atacama, suggesting extensive eolian reworking of salar salts onto the surrounding landscape. Ultimately, salar salts are precipitated from evaporated ground water, which has acquired its dissolved solutes from water-rock interactions (both high and low-temperature) along flowpaths from recharge areas in the Andes. Therefore, the main source for Ca and S in gypsum/anhydrite in non-coastal soils is indirect and involves bedrock alteration, not surficially on the hyperarid landscape, but in the subsurface by ground water

  8. 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.

  9. 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.

  10. 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.

  11. 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

  12. Strontium isotope characterization and major ion geochemistry of karst water flow, Shentou, northern China

    NASA Astrophysics Data System (ADS)

    Wang, Yanxin; Guo, Qinghai; Su, Chunli; Ma, Teng

    2006-09-01

    SummaryKarst water is the most important source of water supply for Shanxi province, northern China. The Shentou springs are representative of the 19 major karst springs at Shanxi. The total area of the Shentou karst water system is 5316 km 2, the Middle Ordovician limestone being its major karst aquifer. In this study, data about the strontium isotope geochemistry and major ion hydrochemistry were analyzed to understand the flow patterns and hydrogeochemical processes of karst water at Shentou. The contour map of TDS value of karst water and that of Sr concentration are similar, showing the general tendency of increase from the northern, western and southern boundary to the discharge area. The average values of 87Sr/ 86Sr ratios of karst water decrease from recharge (0.7107) to discharge area (0.7102), evolving towards those of limestone hostrocks. Comparison of 87Sr/ 86Sr ratios with Sr content suggests that isotopic compositions of some karst water samples from the recharge and flow through area should be the result of interaction between aquifer limestone matrix and strontium-poor recharge waters of meteoric origin. However, for samples from the discharge area that are plotted above the mixing line, mixing with groundwater in the Quaternary aquifers with high 87Sr/ 86Sr ratios may be another factor controlling Sr isotope chemistry. Two major groundwater flow paths were discerned from hydrogeological and geochemical data. Along both flow paths, the 87Sr/ 86Sr ratios of karst water show a general tendency of decrease. Geochemical modeling of the major ion geochemistry of karst water using PHREEQC also indicates that the chemistry of springs should be affected by the incorporation of groundwater in Quaternary aquifer. The effect of the mixing action on the spring hydrochemistry in flow path 1 is more remarkable than that in flow path 2, according to different mixing ratios in both paths (30% in flow path 1 and 5% in flow path 2).

  13. 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.

  14. Mineral dissolution in the Cape Cod aquifer, Massachusetts, USA: I . Reaction stoichiometry and impact of accessory feldspar and glauconite on strontium isotopes, solute concentrations, and REY distribution

    NASA Astrophysics Data System (ADS)

    Bau, Michael; Alexander, Brian; Chesley, John T.; Dulski, Peter; Brantley, Susan L.

    2004-03-01

    To compare relative reaction rates of mineral dissolution in a mineralogically simple groundwater aquifer, we studied the controls on solute concentrations, Sr isotopes, and rare earth element and yttrium (REY) systematics in the Cape Cod aquifer. This aquifer comprises mostly carbonate-free Pleistocene sediments that are about 90% quartz with minor K-feldspar, plagioclase, glauconite, and Fe-oxides. Silica concentrations and pH in the groundwater increase systematically with increasing depth, while Sr isotopic ratios decrease. No clear relationship between 87Sr/ 86Sr and Sr concentration is observed. At all depths, the 87Sr/ 86Sr ratio of the groundwater is considerably lower than the Sr isotopic ratio of the bulk sediment or its K-feldspar component, but similar to that of a plagioclase-rich accessory separate obtained from the sediment. The Si- 87Sr/ 86Sr-depth relationships are consistent with dissolution of accessory plagioclase. In addition, solutes such as Sr, Ca, and particularly K show concentration spikes superimposed on their respective general trends. The K-Sr- 87Sr/ 86Sr systematics suggests that accessory glauconite is another major solute source to Cape Cod groundwater. Although the authigenic glauconite in the Cape Cod sediment is rich in Rb, it is low in in-grown radiogenic 87Sr because of its young Pleistocene age. The low 87Sr/ 86Sr ratios are consistent with equilibration of glauconite with seawater. The impact of glauconite is inferred to vary due to its variable abundance in the sediments. In the Cape Cod groundwater, the variation of REY concentrations with sampling depth resembles that of K and Rb, but differs from that of Ca and Sr. Shale-normalized REY patterns are light REY depleted, show negative Ce anomalies and super-chondritic Y/Ho ratios, but no Eu anomalies. REY input from feldspar, therefore, is insignificant compared to input from a K-Rb-bearing phase, inferred to be glauconite. These results emphasize that interpretation of

  15. The Sr isotope composition of the world ocean, marginal and inland seas: Implications for the Sr isotope stratigraphy

    NASA Astrophysics Data System (ADS)

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

    2012-11-01

    We studied the Sr isotope composition of shells of modern shallow-water mollusks and coral fragments. Twenty five of the studied samples were collected in beach zones of open oceans and marginal seas; twelve and eight additional samples are from saline and freshened inland seas respectively. The 87Sr/86Sr ratio in samples from the Atlantic, Indian, and Pacific oceans and their marginal seas corresponds on average to 0.709202 ± 0.000003 and coincides with the average ratio in the standard USGS EN-1 sample. The average 87Sr/86Sr ratio in inner parts of evaporite subbasins of the Mediterranean and Red seas is identical to that of the oceanic water. In shells of shallow-water mollusks from the Black Sea and Sea of Azov, where the degree of seawater dilution by riverine runoff is as high as 50 to 70%, the 87Sr/86Sr ratio is lower than that in the oceans by only a value of 0.00002 on average. As oceanic waters penetrated into these freshwater basins no earlier than in the Holocene, we conclude that the Sr isotopic equilibration with the oceanic water is realized very rapidly in the epicontinental seas even under conditions of restricted water exchange with the World Ocean. The established uniformity of the Sr isotope composition in all geographic types of currently existing sea basins open to the World Ocean proves the efficiency of the Sr isotope stratigraphy in correlation of contemporaneous chemogenic sediments.

  16. 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).

  17. Strontium isotopes evolution of groundwater in a floodplain, Rio Icacos, Luquillo Experimental Forest, Puerto Rico

    NASA Astrophysics Data System (ADS)

    Feng, X.; Sharma, M.; Landis, J. D.; Gazis, C.; Posmentier, E.; McDowell, W. H.

    2005-12-01

    Major element and Sr concentrations and 87Sr/86Sr ratios were measured in groundwater, rainwater and stream samples collected in2004 from Luquillo Experimental Forest (LEF), Puerto Rico. The groundwater was obtained from wells augured across a ~20 m wide floodplain, which lies between a tributary of Rio Iacos and upslope forest (McDowell et al., Biogeochem 18:53, 1992). The Sr isotope data were also obtained on archived samples collected from the same sites in 1989-1991. The purpose of this study was to investigate (a) controls on the evolution of Sr2+ and their variation between 1989-91 and 2004 and (b) the extent to which floodplain weathering governs the 87Sr/86Sr ratio of the stream. The subsurface water at this site flows through a deep layer of coarse sand and the water table has a gradient of ~0.25. A subset of the data is given below; 1989-91 data are weighted averages of the analyzed samples. % Table generated by Excel2LaTeX from sheet 'Sheet1' \\begin{tabular}{lllll} \\hline Sample & 2004 & 2004 & 1989-91 & 1989-92 & [Sr], ppb & 87Sr/86Sr & [Sr], ppb & 87Sr/86Sr \\hline Rainwater & 4.6 & 0.7101 & & Well (I-9, =4.3 m) & 10.1 & 0.71351 & 1.2 & 0.70875 Well (I-2,d =3.0m) & 18.8 & 0.71035 & & Well (I-4, d= 3.0 m) & 18.1 & 0.70879 & 9.4 & 0.70523 Stream (I-0) & 16.8 & 0.7063 & 15.5 & 0.70512 Downstream of I-0 & 21.5 & 0.70536 & & \\hline The rainwater sample is highly enriched in Sr and has an 87Sr/86Sr ratio higher than seawater; the latter possibly reflects a contribution from Saharan dust. Extreme gradients in 87Sr/86Sr are present in waters from both 2004 and 1989-91 with the samples becoming less radiogenic towards the stream. This is accompanied by a 2 to 5 fold increase in the Sr content. It is evident that most of the stream water Sr is derived from subsurface water, which is significantly modified within the floodplain. The floodplain soil is derived from alteration of quartz diorite bedrock containing biotite, hornblende, plagioclase and quartz

  18. 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.

  19. Determination of initial Sr-isotope compositions of dolostones from the Burlington-Keokuk Formations (Mississippian) of Iowa, Illinois, and Missouri

    SciTech Connect

    Banner, J.L.; Hanson, G.N.; Meyers, W.J.

    1986-05-01

    Sr-isotope compositions, and Rb and Sr concentrations were measured on fine-grained, nearly pure dolostones, each consisting predominantly of one cathodoluminescent generation of dolomite. The results differ significantly, depending on the dissolution method used. For example, one sample gives replicate /sup 87/Sr//sup 86/Sr analyses by leaching with 1.25N HCl of 0.71032 and 0.71062. Adding HF to the leaching process gave a value of 0.71216, whereas complete dissolution with concentrated HF, HNO/sub 3/, and HCl yields a value of 0.71219. Using the time of dolomitization with Rb (12.4 ppm) and Sr (59.7 ppm) concentrations for the completely dissolved sample gives an initial /sup 87/Sr//sup 86/Sr ratio of 0.70943. Similar results for other samples indicate that most Rb and radiogenic Sr are associated with minor clay fractions (predominantly glauconite) in the samples, and that HCl leaches Rb and Sr from clays to a variable extent. Morphologic relationships between dolomite, calcite, and nonpelloidal glauconite suggest that some clay formed episodically during various stages of nonmarine diagenesis. Sr-isotopic exchange may have occurred between carbonate and clay during major influxes of diagenetic fluids. To obtain initial /sup 87/Sr//sup 86/Sr ratios on samples that are completely dissolved, the following corrections are needed: isotopic equilibration between carbonate and clay, closure of the Rb-Sr system after diagenesis, and constraints on the timing of diagenesis. Such initial /sup 87/Sr//sup 86/Sr ratios give the isotopic composition of the carbonate phase at the time of its crystallization, whereas leaching with weak acid is not always carbonate selective and can produce ambiguous results.

  20. 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.

  1. 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.

  2. 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

  3. 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.

  4. 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.

  5. 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

  6. 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.

  7. Geochemical and Isotopic Data from Micron to Across-Arc Scales in the Andean Central Volcanic Zone: Applications for Resolving Crustal Magmatic Differentiation and Modification Processes

    NASA Astrophysics Data System (ADS)

    Michelfelder, G.; Wilder, A.; Feeley, T.

    2014-12-01

    Plagioclase crystals from silicic (andesitic to dacitic) lavas and domes at Volcán Uturuncu, a potentially active volcano in the back-arc of the Andean CVZ (22.3°S, 67.2°W), exhibit large variations in An contents, textures, and core to rim 87Sr/86Sr ratios. Many of the isotopic variations can not have existed at magmatic temperatures for more than a few thousand years. The crystals likely derived from different locations in the crustal magmatic system and mixed just prior to eruption. Uturuncu magmas initially assimilated crustal rocks with high 87Sr/86Sr ratios. The magmas were subsequently modified by frequent recharge of more mafic magmas with lower 87Sr/86Sr ratios. A typical Uturuncu silicic magma therefore only attains its final composition just prior to or during eruption. In the Lazufre region of active surface uplift (~25˚14'S; Volcán Lastarria and Cordon del Azufre) closed system differentiation processes are not the only factors influencing silicic magma compositions. 87Sr/86Sr (0.70651-0.70715) and 206Pb/204Pb ratios (18.83-18.88) are highly elevated and143Nd/144Nd ratios (0.512364 -0.512493) are low relative to similar composition rocks from the "southern Cordillera domain." These data, along with major and trace element trends, reflect a multitude of differentiation processes and magma sources including crystallization-differentiation of more mafic magmas, melting and assimilation of older crustal rocks, and magma mixing and mingling. On an arc-wide scale silicic lavas erupted from three well-characterized composite volcanoes between 21oS and 22oS (Aucanquilcha, Ollagüe, and Uturuncu) display systematically higher K2O, LILE, REE and HFSE contents and 87Sr/86Sr ratios with increasing distance from the arc-front. In contrast, the lavas have systematically lower Na2O, Sr, and Ba contents; LILE/HFSE ratios; 143Nd/144Nd ratios; and more negative Eu anomalies. Silicic magmas along the arc-front apparently reflect melting of relatively young, mafic

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

    NASA Astrophysics Data System (ADS)

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

    1996-10-01

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

  9. 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.

  10. 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.

  11. Rb-Sr geochronology of the region between the Antarctic Peninsula and the Transantarctic Mountains: Haag nunataks and Mesozoic granitoids

    NASA Astrophysics Data System (ADS)

    Millar, I. L.; Pankhurst, R. J.

    Seventy-two new Rb-Sr whole-rock analyses are reported for Haag Nunataks, Mount Woollard, the Whitmore Mountains, the Pirrit and Nash hills, and Pagano Nunatak. For Haag Nunataks, three isochrons for gneisses and later aplogranite and microgranite sheets establish the age of crustal formation as 1000-1100 Ma. No other basement rocks of this age are known from the Antarctic Peninsula or Ellsworth Land. Results from the migmatite-pegmatite complex at Mount Woollard are inconclusive but do not suggest that this represents Precambrian crystalline basement. Provisional results for the Whitmore Mountains granites are compatible with crystallization of all components within error of a 182±5 Ma isochron for fine-grained microgranite, but variation in initial 87Sr/86Sr from 0.707 for porphyritic granites to 0.722 for the microgranite rule out simple crystal fractionation models which require a common parental magma. The granites of the Ellsworth-Thiel mountains ridge are well dated as Middle Jurassic by the new data: Pirrit Hills 173±3 Ma, Nash Hills 175±8 Ma, and Pagano Nunatak 175±8 Ma. Initial 87Sr/86Sr ratios of 0.707, 0.712, and 0.716, respectively, confirm that these are intracratonic S-type granites with a large crustal component involved in magma generation. The dolerite of Lewis Nunatak is shown by its Rb, Sr, and 87Sr/86Sr composition to be a member of the Jurassic Ferrar Supergroup.

  12. Effect of sea water interaction on strontium isotope composition of deep-sea basalts

    USGS Publications Warehouse

    Julius, Dasch E.; Hedge, C.E.; Dymond, J.

    1973-01-01

    Analyses of rim-to-interior samples of fresh tholeiitic pillow basalts, deuterically altered holocrystalline basalts, and older, weathered tholeiitic basalts from the deep sea indicate that 87Sr 86Sr ratios of the older basalts are raised by low temperature interaction with strontium dissolved in sea water. 87Sr 86Sr correlates positively with H2O in these basalts; however, there is little detectable modification of the strontium isotope composition in rocks with H2O contents less than 1%. The isotope changes appear to be a function of relatively long-term, low-temperature weathering, rather than high-temperature or deuteric alteration. Strontium abundance and isotopic data for these rocks suggest that strontium content is only slightly modified by interaction with sea water, and it is a relatively insensitive indicator of marine alteration. Average Rb-Sr parameters for samples of apparently unaltered basalt are: Rb = 1.11 ppm; Sr = 132 ppm; 87Sr 86Sr = 0.70247. ?? 1973.

  13. 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.

  14. 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.

  15. 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.

  16. 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

  17. 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

  18. 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

  19. 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

  20. Isotope and chemical microsampling: Constraints on the history of an S-type rhyolite, San Vincenzo, Tuscany, Italy

    NASA Astrophysics Data System (ADS)

    Feldstein, S. N.; Halliday, A. N.; Davies, G. R.; Hall, C. M.

    1994-01-01

    Fine scale heterogeneities in strontium isotope ratios, 40Ar- 39Ar ages, and chemical composition have been determined for individual mineral grains and enclaves in the rhyolites of San Vincenzo, Italy. The rhyolites are peraluminous with phenocrysts of alkali feldspar, plagioclase, biotite, and cordierite and have previously been divided into two groups on the basis of whole rock major element chemistry. Group B lavas are distinguished from Group A in having higher MgO and CaO contents as well as containing two pyroxenes and chilled latite enclaves. The Group B lavas show textural evidence for disequilibrium, such as resorption and sieve zones in feldspars. Laser fusion 40Ar- 39Ar dating of individual alkali feldspar crystals suggests that the eruption of these rhyolites took place 4.38 ± 0.04 Ma, although small amounts of excess argon are present in subhedral and cloudy crystals. The groundmass in the Group A sample has a higher initial 87Sr /86Sr (0.725) than that of the Group B (0.713). The Sr isotope compositions of chemically and texturally characterized individual grains reveal marked disequilibrium between minerals and the host glass as well as within-grain zonation. The feldspars and coarse-grained biotites have initial 87Sr /86Sr that are intermediate between those of the Group A and B glasses, with alkali feldspar generally having higher initial 87Sr /86Sr ratios than plagioclase. Chilled latite enclaves, which are present in only the Group B lavas, have relatively low initial 87Sr /86Sr ratios in the range 0.7082-0.7088. The mineral chemistry and isotope data indicate that restite does not form a significant portion of the crystalline assemblage and, therefore, cannot be the source of the strontium isotope disequilibrium. Xenocrysts mixed into the rhyolite from a mafic magma were identified as clinopyroxene megacrysts, clinopyroxene-orthopyroxene clots, orthopyroxene-plagioclase clots, and plagioclase with extensive sieve textures. These grains all

  1. Variability of sulphur isotope ratios in pyrite and dissolved sulphate in granitoid fractures down to 1 km depth - Evidence for widespread activity of sulphur reducing bacteria

    NASA Astrophysics Data System (ADS)

    Drake, Henrik; Åström, Mats E.; Tullborg, Eva-Lena; Whitehouse, Martin; Fallick, Anthony E.

    2013-02-01

    Euhedral pyrite crystals in 46 open bedrock (granitoid) fractures at depths down to nearly 1 km were analysed for sulphur isotope ratios (δ34S) by the in situ secondary ion mass spectrometry (SIMS) technique and by conventional bulk-grain analysis, and were compared with groundwater data. Twenty nine of the fractures sampled for pyrite had corresponding data for groundwater, including chemistry and isotopic ratios of sulphate, which provided a unique opportunity to compare the sulphur-isotopic ratios of pyrite and dissolved sulphate both at site and fracture-specific scales. Assessment of pyrite age and formation conditions were based on the geological evolution of the area (Laxemar, SE Sweden), and on data on co-genetic calcite as follows: (1) the isotopic ratios of the calcite crystals (δ18O, δ13C, 87Sr/86Sr) were compared with previously defined isotopic features of fracture mineral assemblages precipitated during various geological periods, and (2) the δ18O of the calcites were compared with the δ18O of groundwater in fractures corresponding to those where the calcite/pyrite assemblages were sampled. Taken together, the data show that all the sampled fractures carried pyrite/calcite that are low-temperature and precipitated from the current groundwater or similar pre-existing groundwater, except at depths of -300 to -600 m where water with a glacial component dominates and the crystals are from pre-modern fluids. An age of <10 Ma are anticipated for the pre-modern fluids. The δ34Spyr showed huge variations across individual crystals (such as -32 to +73‰) and extreme minimum (-50‰) and maximum (+91‰) values. For this kind of extreme S-isotopic variation at earth-surface conditions there is no other explanation than activity of sulphur reducing bacteria coupled with sulphate-limited conditions. Indeed, the most common subgrain feature was an increase in δ34Spyr values from interior to rim of the crystal, which we interpret are related to successively

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

    NASA Astrophysics Data System (ADS)

    Rossi, Carlos; Vilas, Lorenzo; Arias, Consuelo

    2015-10-01

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

  3. Termination of a Central Andean arc: The Chemical Evolution of the Bonete-Incapillo Volcanic Complex, Argentina

    NASA Astrophysics Data System (ADS)

    Goss, A. R.; Kay, S. M.

    2003-12-01

    The Bonete-Incapillo Volcanic Complex is situated near 28° S at the southern termination of the Central Volcanic Zone (CVZ), where the more steeply-dipping segment of the subducting Nazca Plate to the north intersects the amagmatic flatslab to the south. Dominated by the Pissis (6882m), Bonete Chico (6759m), and Bonete Grande (6436m) centers and the Incapillo Caldera, this complex includes some of the highest Plio-Pleistocene volcanoes on Earth. K-Ar ages indicate that volcanism in this region began at 6.5 to 3.5 Ma as the Miocene magmatic arc to the west broadened and eventually died out. During this period, the subducting Nazca Plate shallowed, initiating eastward broadening of the arc. The arc front migrated 50km to the east before terminating at this latitude with the formation of the Incapillo Caldera at 2.9 to 1.1 Ma. Nearly 80 major and trace element analyses from the Bonete Complex and the associated Pircas Negras andesitic lavas combined with 35 new 87Sr/86Sr analyses allow for interpretation of the regional geochemical evolution. Prior to arc migration, the Miocene Doña Ana Formation lavas that erupted in this region have 87Sr/86Sr ratios (0.7047-0.7056) that positively correlate with SiO2 content (56-74 %), suggesting that MASH-style crustal contamination was a dominant process in magma evolution. In contrast, the Late Miocene to Pliocene magmas from the Bonete Complex and Pircas Negras units show a range of 87Sr/86Sr ratios (0.7057-0.7073) in samples with uniform SiO2 contents. Unlike the older Doña Ana magmas and <3 Ma CVZ magmas further north, these migration-stage magmas exhibit steep `adakitic' REE patterns (La/Yb = 40-70) indicating equilibration with garnet-bearing crust. These steep REE patterns and elevated 87Sr/86Sr ratios are consistent with source region contamination by forearc subduction erosion that resulted in transport of the missing Mesozoic igneous and forearc suites along the Chilean coast into the melt zone of the mantle wedge. A

  4. 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.

  5. 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.

  6. 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

  7. 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

  8. Dissolved strontium in the subterranean estuary - Implications for the marine strontium isotope budget

    NASA Astrophysics Data System (ADS)

    Beck, Aaron J.; Charette, Matthew A.; Cochran, J. Kirk; Gonneea, Meagan E.; Peucker-Ehrenbrink, Bernhard

    2013-09-01

    Submarine groundwater discharge (SGD) to the ocean supplies Sr with less radiogenic 87Sr/86Sr than seawater, and thus constitutes an important term in the Sr isotope budget of the modern ocean. However, few data exist for Sr in coastal groundwater or in the geochemically dynamic subterranean estuary (STE). We examined Sr concentrations and isotope ratios from nine globally-distributed coastal sites and characterized the behavior of Sr in the STE. Dissolved Sr generally mixed conservatively in the STE, although large differences were observed in the meteoric groundwater end-member Sr concentrations among sites (0.1-24 μM Sr). Strontium isotope exchange was observed in the STE at five of the sites studied, and invariably favored the meteoric groundwater end-member signature. Most of the observed isotope exchange occurred in the salinity range 5-15, and reached up to 40% exchange at salinity 10. Differences in fresh groundwater Sr concentrations and isotope ratios (87Sr/86Sr = 0.707-0.710) reflected aquifer lithology. The SGD end-member 87Sr/86Sr must be lower than modern seawater (i.e., less than 0.70916) in part because groundwater Sr concentrations are orders of magnitude higher in less-radiogenic carbonate and volcanic island aquifers. A simple lithological model and groundwater Sr data compiled from the literature were used to estimate a global average groundwater end-member of 2.9 μM Sr with 87Sr/86Sr = 0.7089. This represents a meteoric-SGD-driven Sr input to the ocean of 0.7-2.8 × 1010 mol Sr y-1. Meteoric SGD therefore accounts for 2-8% of the oceanic Sr isotope budget, comparable to other known source terms, but is insufficient to balance the remainder of the budget. Using reported estimates for brackish SGD, the estimated volume discharge at salinity 10 (7-11 × 1015 L y-1) was used to evaluate the impact of isotope exchange in the STE on the brackish SGD Sr flux. A moderate estimate of 25% isotope exchange in the STE gives an SGD Sr end-member 87Sr/86Sr

  9. 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.

  10. 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

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

    NASA Astrophysics Data System (ADS)

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

    2011-12-01

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

  12. 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

  13. 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

  14. 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.

  15. 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.

  16. Strontium isotopic geochemistry of the Devils Lake drainage system, North Dakota: A preliminary study and potential paleoclimatic implications

    USGS Publications Warehouse

    Lent, R.M.; Gaudette, H.E.; Lyons, W.B.

    1997-01-01

    A series of water samples (precipitation, surface water and ground water) from the Devils Lake drainage basin in central North Dakota have been analyzed for their ??180 and ??D and 87Sr/86Sr. The ??180 and ??D of snow and most ground water samples fall near the meteoric water line, with the ground water being isotopically heavier than the snow, indicating that a portion of the recharge must come from non-winter precipitation events. One ground water and all the surface water samples fall below the meteoric water line, demonstrating extensive evaporation. The 87Sr/86Sr ratio of the snow is more radiogenic than those of the ground water samples, indicating that the ground water has increased its 86Sr content by the dissolution of mafic rock in the aquifer. Stump Lake has a much inure radiogenic Sr isotopic ratio than the waters of Devils Lake suggesting a source of water different from that of Devils Lake. The East Stump Lake water, on the other hand, appears to be either a mix of Devils Lake and Stump Lake waters, or Devils Lake water diluted with precipitation.

  17. 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

  18. Elemental and strontium isotopic geochemistry of the soil profiles developed on limestone and sandstone in karstic terrain on Yunnan-Guizhou Plateau, China: Implications for chemical weathering and parent materials

    NASA Astrophysics Data System (ADS)

    Liu, Wen-Jing; Liu, Cong-Qiang; Zhao, Zhi-Qi; Xu, Zhi-Fang; Liang, Chong-Shan; Li, Long-bo; Feng, Jia-Yi

    2013-05-01

    The limestone and yellow sandstone soil profiles from SW China were measured for chemical and Sr isotope compositions of the bulk soils and their sequential leachates (labile, carbonate, and residue or silicate fraction), aiming to characterize the parent materials of the soils, to understand the soil weathering and formation processes, and to discuss the origin of the red residua (terra rossa). The studied yellow sandstone soil, yellow limestone soil, and black limestone soil show different pH values, SiO2 contents, Rb/Sr abundance ratios, and 87Sr/86Sr ratios. The sequential leachates of different soil types also have different 87Sr/86Sr and Ca/Sr ratios. The major chemical compositions of the studied soil profiles suggest that all the sandstone and limestone soils are developing at a stage that feldspar is exhausting and the clay minerals are changing from smectite to kaolinite and gibbsite. As compared with the red residua distributed in the karst region, the soils studied here show lower CIA values (58-84), but both higher Na2O/K2O (0.9-2.7) and Na2O/Al2O3 concentration ratios (0.07-0.26) on average, suggesting a lower weathering intensity than that of the red residua. The depth profiles of soil CIA values, Na2O/K2O and Rb/Sr ratios, and 87Sr/86Sr ratios indicate that the weathering intensity is slightly lower for the upper and higher for the deeper soils, which suggest that the sandstone and limestone soil profiles were formed through both accumulation and weathering of in situ weathering residue and input of external detritus or soil from upper land. During weathering of the soils, preferential release of Ca and retention of Sr in soil result in higher Ca/Sr ratios in both labile and carbonate fractions than those in the residue fractions of all soil profiles. The co-variations of Hf/Nb and Zr/Nb ratios, together with those Rb/Sr and 87Sr/86Sr ratios of limestone soils, sandstone soils, and the red residua, demonstrate that their parent materials are

  19. Calculation of simultaneous isotopic and trace element variations during water-rock interaction with applications to carbonate diagenesis

    SciTech Connect

    Banner, J.L. ); Hanson, G.N. )

    1990-11-01

    Equations are developed for the calculation of the simultaneous variations in trace element concentrations and radiogenic and stable isotopic compositions that occur during water-rock interaction. The equations are of general use for modeling chemical and isotopic variations in porous media and are applied here to the diagenesis of carbonate rocks and sediments. Owing to the extreme differences in the concentrations of oxygen and carbon in diagenetic fluids, carbonate minerals equilibrate with fluid {delta}{sup 18}O values at three orders of magnitude lower waterrock ratios (< 10) than the waterrock ratios at which they equilibrate with fluid {delta}{sup 13}C values (10{sup 3}). {sup 87}Sr/{sup 86}Sr ratios are affected at variable rates. In order to reset the {sup 87}Sr/{sup 86}Sr value of a marine limestone during freshwater diagenesis, waterrock ratios similar to those calculated for equilibration of {delta}{sup 13}C values are required, while Sr-Ca-rich brines can reset the {sup 87}Sr/{sup 86}Sr value of a limestone at low waterrock ratios, similar to those calculated for equilibration of {delta}{sup 18}O values. These large, relative differences in the response of different isotopic systems to water-rock interaction translate into characteristic trends on isotope and trace element covariation diagrams that can be used to distinguish between (1) different models for water-rock interaction and (2) different processes such as water-rock interaction, mixing of fluids, and mixing of mineral endmembers. These modeling approaches are applied to the regionally extensive dolomites of the Mississippian Burlington-Keokuk Formation.

  20. 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

  1. Sr isotopic variations along the Juan de Fuca Ridge.

    USGS Publications Warehouse

    Eaby, J.; Clague, D.A.; Delaney, J.R.

    1984-01-01

    The Sr isotopic ratios of 39 glass and microcrystalline basalt samples along the Juan de Fuca Ridge and one glass sample from Brown Bear Seamount are at the lower end of the range for normal MORB; the average 87Sr/86Sr ratio is 0.70249 + or - 0.00014 (2sigma ). Although subtle variations exist along the strike of the ridge, the Sr isotopic data do not show systematic variation relative to the proposed Cobb hotspot. The isotopic data are inconsistent with an enriched mantle-plume origin for the Cobb-Eikelberg Seamount chain.-W.H.B.

  2. The Sahara-East Mediterranean dust and climate connection revealed by strontium and uranium isotopes in a Jerusalem speleothem

    NASA Astrophysics Data System (ADS)

    Frumkin, Amos; Stein, Mordechai

    2004-01-01

    This paper explores the potential of Sr and U isotope systems in speleothems as tracers of eolian dust transport and hydrological conditions. The study focuses on a speleothem from Jerusalem spanning the past 220 kyr. This speleothem provides a precisely dated record of dust flux from the Sahara to the East Mediterranean. Enhanced dust flux and Terra Rossa soil development are reflected by elevated 87Sr/ 86Sr ratios in the speleothem (0.7082-0.7086), while lower 87Sr/ 86Sr ratios (˜0.7078) indicate higher contribution of the local bedrock due to low dust flux and low soil accumulation. The strontium isotope system in the speleothem is a robust monitor of the Sahara monsoon-modulated climate, since dust uptake is related to development or reduction in vegetation cover of Sahara soil. The [ 234U/ 238U] activity ratios in the speleothem range between 1.12 and 1.0. The high activity values may indicate selective removal of 234U from the soil while the low values converge to the bedrock. The migration of 234U to the cave reflects mainly the regional hydrological conditions that are modulated by the North Atlantic-Mediterranean climate system. Thus, the speleothem provides a combined record of the monsoon-North Atlantic climatic systems. Long-term stability in glacial 87Sr/ 86Sr ratios (0.7083±0.0001 over the past 220 kyr) suggests an overall similarity in eolian dust sources, and uniformity in the synoptic conditions that dominate the dust storm tracks during glacial periods.

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

    NASA Astrophysics Data System (ADS)

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

    2014-11-01

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

  4. 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.

  5. 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

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

    NASA Astrophysics Data System (ADS)

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

    2002-12-01

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

  7. 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

  8. 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.

  9. 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.

  10. 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.

  11. 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

  12. Mg Isotope variations of Marinoan Cap Carbonates: implications for the chemical evolution of Neoproterozoic Ocean after snowball earth

    NASA Astrophysics Data System (ADS)

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

    2012-12-01

    We report Mg isotope profiles of two cap-carbonates: Nuccaleena formation from south Australia (mostly dolostones) and Tsagaan Oloom Formation from southwest Mongolia (including dolostones, aragonite crystal fans, and lime-mudstones). These data provide additional constraints on the chemical evolution of Neoproterozoic Oceans after the Marinoan deglaciation. An incremental leaching technique using ammonium acetate and various concentrations of acetic acid and hydrochloric acid was applied to separate metals in various forms from cap-carbonates (including surface adsorbed phases, calcite, dolomite and clay minerals). The leachates were then passed through chromatographic columns to extract pure Mg and Sr, which were then analyzed for their isotopic compositions by MC-ICP-MS (Neptune) at Yale University. Elemental ratios (Mg/Ca and Sr/Ca) in each leaching steps were also measured. Our results show that small variations of δ26MgDSM3 with leaching steps were observed in most dolostone samples when secondary calcite is absent. In contrast, large Mg isotope variations (up to 1.5 per mil) were shown in the leaching steps of limestone and crystal fans. The primary δ26MgDSM3 value of each sample was chosen from the leachate that has the lowest 87Sr/86Sr ratios. The δ26MgDSM3 value of Nuccaleena dolostone increases from -2.2‰ at the basal part of the section to -1.7‰ in the middle, and then turns back to -2.0‰ on the top, with a positive correlation between 26Mg/24Mg and 87Sr/86Sr ratios, implying that the high δ26MgDSM3 values may be caused by alteration or inherit from continental-derived fluids. In contrast, small δ26MgDSM3 variations in Tsagaan Oloom dolostones were exhibited in different leaching steps or cross the section (~-1.7‰), with high 87Sr/86Sr ratios (~0.7090), resembling cap dolostones from middle part of Nuccaleena dolostone, implying that they are formed in a similar environment. However, the δ26MgDSM3 value of upper lime-mudstones and crystal

  13. 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.

  14. 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

  15. 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

  16. 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

  17. 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

  18. Reconciling the elemental and Sr isotope composition of Himalayan weathering fluxes: insights from the carbonate geochemistry of stream waters

    NASA Astrophysics Data System (ADS)

    Jacobson, Andrew D.; Blum, Joel D.; Walter, Lynn M.

    2002-10-01

    Determining the relative proportions of silicate vs. carbonate weathering in the Himalaya is important for understanding atmospheric CO 2 consumption rates and the temporal evolution of seawater Sr. However, recent studies have shown that major element mass-balance equations attribute less CO 2 consumption to silicate weathering than methods utilizing Ca/Sr and 87Sr/ 86Sr mixing equations. To investigate this problem, we compiled literature data providing elemental and 87Sr/ 86Sr analyses for stream waters and bedrock from tributary watersheds throughout the Himalaya Mountains. In addition, carbonate system parameters (P CO 2, mineral saturation states) were evaluated for a selected suite of stream waters. The apparent discrepancy between the dominant weathering source of dissolved major elements vs. Sr can be reconciled in terms of carbonate mineral equilibria. Himalayan streams are predominantly Ca 2+-Mg 2+-HCO 3- waters derived from calcite and dolomite dissolution, and mass-balance calculations demonstrate that carbonate weathering contributes ˜87% and ˜76% of the dissolved Ca 2+ and Sr 2+, respectively. However, calculated Ca/Sr ratios for the carbonate weathering flux are much lower than values observed in carbonate bedrock, suggesting that these divalent cations do not behave conservatively during stream mixing over large temperature and P CO 2 gradients in the Himalaya. The state of calcite and dolomite saturation was evaluated across these gradients, and the data show that upon descending through the Himalaya, ˜50% of the streams evaluated become highly supersaturated with respect to calcite as waters warm and degas CO 2. Stream water Ca/Mg and Ca/Sr ratios decrease as the degree of supersaturation with respect to calcite increases, and Mg 2+, Ca 2+, and HCO 3- mass balances support interpretations of preferential Ca 2+ removal by calcite precipitation. On the basis of patterns of saturation state and P CO 2 changes, calcite precipitation was estimated

  19. Geochemistry and zircon ages of mafic dikes in the South Qinling, central China: evidence for late Neoproterozoic continental rifting in the northern Yangtze block

    NASA Astrophysics Data System (ADS)

    Zhu, Xiyan; Chen, Fukun; Liu, Bingxiang; Zhang, He; Zhai, Mingguo

    2015-01-01

    Neoproterozoic volcanic-sedimentary sequences of the southern Qinling belt, central China, were intruded by voluminous mafic dikes. secondary ion mass spectrometry zircon U-Pb dating indicates that these dikes were emplaced at 650.8 ± 5.2 Ma, coeval with mafic rocks occurring at the northern margin of the Yangtze block. The dikes are characterized by enrichment of large ion lithophile elements, high Ti contents (up to 3.73 wt%) and Nb/Ta ratios between 14.5 and 19.6, suggesting a mantle source of oceanic island basalt affinity. Initial 87Sr/86Sr ratios show positive correlation with SiO2 contents and negative correlation with Zr/Nb ratios, implying that these rocks were affected by crustal contamination during the magma ascend and emplacement process. The dikes have initial ɛ Nd values of +0.2 to +3.3, low 206Pb/204Pb ratios of 16.96-17.45, and moderate 87Sr/86Sr ratios of 0.7043-0.7076, likely pointing to the involvement of an enriched mantle source. The mafic dikes and coeval mafic volcanic equivalents in the South Qinling and the northern Yangtze are hypothesized to be related with the prolonged breakup of the supercontinent Rodinia, suggesting that continental rifting lasted until ca. 650 Ma.

  20. The Change in Black Sea Water Composition and Hydrology during Deglaciation from Multiproxy Reconstructions

    NASA Astrophysics Data System (ADS)

    Yanchilina, A.; Ryan, W. B. F.; McManus, J. F.

    2014-12-01

    This study presents a reconstruction of changes in the water column from the last glacial into the early Holocene using stable isotope, 87Sr/86Sr, 14C, and trace element ratios from mollusks from the shelf area and ostracods from the basin of the Black Sea. The stable isotope record is compared to a thoroughly U/Th dated terrestrial stable isotope record of a nearby cave, Sofular cave in northwestern Turkey. The combination of deep, surface, and terrestrial signals gives valuable insight towards the behavior of the lake water during the deglaciation in multiple dimensions, specifically the water column stratification and hydrological dynamics. The comparison of the stable isotope records of two independent proxies allows to make inferences on the changes in the 14C reservoir of the Black Sea-Lake. Results show that during the glacial period, water from the Black Sea-Lake was outflowing to the Sea of Marmara but the ventilation of the water column was weak as old 14C was not removed and allowed to accumulate giving the lake a large 14C reservoir age. A deglacial pulse of meltwater released from the Eurasian Fennoscandian pro-glacial lakes increased ventilation of the water column. This is seen in lighter δ18O and a spike in radiogenic 87Sr/86Sr in both deep and shallow parts of the water column. The dynamic ventilation and outflow of water into the Sea of Marmara continued until the onset of the Bolling/Allerod as the radiogenic 87Sr/86Sr was almost completely flushed out in a couple hundred years time. During the Bolling/Allerod and Preboreal warming, δ18O got heavier whereas the 87Sr/86Sr stayed constant and the 14C again accumulated and contributed to an older reservoir age. The Younger Dryas period, sandwiched in between the two warming periods, shows a return to glacial conditions in the δ13C and that the water outflowed to the Sea of Marmara as the δ18O only showed a slight change towards a more heavy value.

  1. 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

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

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

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

  3. 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

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

    PubMed

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

    2012-01-01

    Sequential leaching experiments on coal utilization by-products (CUB) were coupled with chemical and strontium (Sr) isotopic analyses to better understand the influence of coal type and combustion processes on CUB properties and the release of elements during interaction with environmental waters during disposal. Class C fly ash tended to release the highest quantity of minor and trace elements-including alkaline earth elements, sodium, chromium, copper, manganese, lead, titanium, and zinc-during sequential extraction, with bottom ash yielding the lowest. Strontium isotope ratios ((87)Sr/(86)Sr) in bulk-CUB samples (total dissolution of CUB) are generally higher in class F ash than in class C ash. Bulk-CUB ratios appear to be controlled by the geologic source of the mineral matter in the feed coal, and by Sr added during desulfurization treatments. Leachates of the CUB generally have Sr isotope ratios that are different than the bulk value, demonstrating that Sr was not isotopically homogenized during combustion. Variations in the Sr isotopic composition of CUB leachates were correlated with mobility of several major and trace elements; the data suggest that arsenic and lead are held in phases that contain the more radiogenic (high-(87)Sr/(86)Sr) component. A changing Sr isotope ratio of CUB-interacting waters in a disposal environment could forecast the release of certain strongly bound elements of environmental concern. This study lays the groundwork for the application of Sr isotopes as an environmental tracer for CUB-water interaction. PMID:22218183

  5. 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.

  6. 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.

  7. 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.

  8. Preliminary results on the oxygen isotopic composition of the lower crust, Kilbourne Hole Maar, New Mexico

    NASA Astrophysics Data System (ADS)

    James, David E.; Padovani, Elaine R.; Hart, Stanley R.

    1980-05-01

    18O/16O ratios measured in deep crustal xenoliths from Kilbourne Hole maar, New Mexico show that the oxygen isotopic composition of the lower crust of that region is grossly heterogeneous. Xenoliths derived from similar crustal depths vary in δ18O by nearly 6‰, although the xenoliths are individually in internal oxygen isotopic equilibrium. Mafic granulites (including charnockite), probably of mantle origin, have δ18O of about 6.2 to 6.3‰ and correspondingly low 87Sr/86Sr ratios (0.703 to 0.707). Garnet granulites, apparently the residue of partial fusion of pelitic sedimentary rock, have δ18O ranging from about 9‰ to 12‰ and correspondingly high 87Sr/86Sr ratios (0.71 to 0.78). No evidence is found for extensive oxygen exchange over large distances in the anhydrous lower crust beneath Kilbourne Hole. Absence of regional isotopic equilibrium indicates that even at melting or near melting temperatures the oxygen isotopic identity of the protolith can be preserved over long periods of time. We conclude that there is little reason to postulate that massive oxygen exchange with a mantle-like reservoir is a general phenomenon of the lower crust.

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

    PubMed Central

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

    2001-01-01

    Between A.D. 900 and 1150, more than 200,000 conifer trees were used to build the prehistoric great houses of Chaco Canyon, New Mexico, in what is now a treeless landscape. More than one-fifth of these timbers were spruce (Picea) or fir (Abies) that were hand-carried from isolated mountaintops 75–100 km away. Because strontium from local dust, water, and underlying bedrock is incorporated by trees, specific logging sites can be identified by comparing 87Sr/86Sr ratios in construction beams 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. PMID:11572943

  10. Boron and strontium isotopic characterization of coal combustion residuals: validation of new environmental tracers.

    PubMed

    Ruhl, Laura S; Dwyer, Gary S; Hsu-Kim, Heileen; Hower, James C; Vengosh, Avner

    2014-12-16

    In the U.S., coal fired power plants produce over 136 million tons of coal combustion residuals (CCRs) annually. CCRs are enriched in toxic elements, and their leachates can have significant impacts on water quality. Here we report the boron and strontium isotopic ratios of leaching experiments on CCRs from a variety of coal sources (Appalachian, Illinois, and Powder River Basins). CCR leachates had a mostly negative δ(11)B, ranging from -17.6 to +6.3‰, and (87)Sr/(86)Sr ranging from 0.70975 to 0.71251. Additionally, we utilized these isotopic ratios for tracing CCR contaminants in different environments: (1) the 2008 Tennessee Valley Authority (TVA) coal ash spill affected waters; (2) CCR effluents from power plants in Tennessee and North Carolina; (3) lakes and rivers affected by CCR effluents in North Carolina; and (4) porewater extracted from sediments in lakes affected by CCRs. The boron isotopes measured in these environments had a distinctive negative δ(11)B signature relative to background waters. In contrast (87)Sr/(86)Sr ratios in CCRs were not always exclusively different from background, limiting their use as a CCR tracer. This investigation demonstrates the validity of the combined geochemical and isotopic approach as a unique and practical identification method for delineating and evaluating the environmental impact of CCRs. PMID:25417938

  11. Sr-Isotope Composition of Feldspar: Implication for age and Evolution of Gabbros from Uralian-Alaskan Type Complexes in the Ural Mountains, Russia

    NASA Astrophysics Data System (ADS)

    Bruegmann, G. E.; Krause, J.; Pushkarev, E.

    2006-12-01

    Compared to whole-rock or bulk mineral analyses single mineral composition could reveal disequilibrium features between crystals or within individual crystals which provide important information on magma chamber processes. We applied a LA-ICPMS technique to determine Sr isotopes in plagioclase and K-feldspar of gabbroic rocks from the Nizhnii Tagil and Kytlym complexes in the Ural Mountains in Russia. These complexes are Uralian-Alaskan-type zoned mafic-ultramafic complexes, consisting of dunite, clinopyroxenite and gabbro bodies. The rock association is considered to represent a cumulate sequence of a single parental melt feeding a magma chamber system. The instruments used were a NU Plasma MC-ICPMS and a solid-state 193 and 213 nm Nd:YAG laser ablation system from New Wave. The data of the present study includes up to five spot analyses (100-120 μm spot size) of each mineral in a thin section. Baselines for analyses were measured on-peak for 20 s while flushing the sample chamber with He. About 300 to 500 isotope ratios were measured during the ablation time of 80-100 s. Raw data were exported to an external data reduction spreadsheet and corrected for interferences (Kr, Rb) and mass bias using 87Sr/^{88}Sr=0.1194. During the time of analyses we measured the Sr isotope composition of an in-house marine carbonate reference material. Its 87Sr/86Sr of 0.70923±6 (2SD) agrees within error limits with our TIMS measurements. The gabbros have porphyric textures with clinopyroxene phenocrysts in a matrix of olivine, clinopyroxene and spinel. Two gabbro types can be distinguished based on additional matrix minerals. One type of gabbro is silica saturated, contains plagioclase (An57-88) and in places orthopyroxene as matrix phases. The second gabbro type is silica undersaturated and contains in the matrix plagioclase (An29-56) and pseudoleucite, a fine grained intergrowth of nepheline and K-feldspar (Or30-81). In this gabbro plagioclase has generally higher Sr

  12. 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.

  13. 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.

  14. 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.

  15. 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.

  16. Petrological and geochemical characteristics of Cenozoic high-K calc-alkaline volcanism in Konya, Central Anatolia, Turkey

    NASA Astrophysics Data System (ADS)

    Temel, Abidin; Gündoğdu, M. Niyazi; Gourgaud, Alain

    1998-10-01

    Late Miocene to Pliocene volcanic rocks outcrop west, northwest and southwest of the Konya area in Central Anatolia, Turkey. Volcanic products are lava domes, nuée ardentes and ignimbrite deposits, predominantly andesitic to dasitic in composition, together with rare basalt, basaltic andesite, basaltic trachyandesite and trachyandesite (50.35-69.39% SiO 2). The serie exhibits high-K calc-alkaline affinities. Fractional crystallization of pyroxene, plagioclase and Fe-Ti oxides is the main process in the magmatic evolution of Konya volcanic rocks. Volcanic units exhibit typical high-K calc-alkaline character. Their geochemical characteristics (e.g., enrichments in LIL elements such as K, Rb, Ba, Sr, depletion in HFSE such as Ti, Nb, and high Ba/Nb and Low Nb/Y ratios) are consistent with those of active continental margin regions. High 87Sr/ 86Sr (0.704841-0.707340) and low 143Nd/ 144Nd (0.512390-0.512618) ratios suggest crustal involvement in their petrogenesis. Correlations between 86Sr/ 87Sr isotope with Rb, Rb/Nb, Rb/Ba, and Rb/Sr also emphasize the effect of crustal contamination on the andesitic and dacitic magmas. As a consequence, Konya volcanic rocks are products of assimilation and fractional crystallization (AFC) processes of a magma which seems to be linked to the subduction of the African plate underneath the Anatolian plate during Miocene.

  17. 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.

  18. 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.

  19. 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.

  20. 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.

  1. 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. PMID:25905785

  2. Reworked old crust-derived shoshonitic magma: The Guarany pluton, Northeastern Brazil

    NASA Astrophysics Data System (ADS)

    Ferreira, Valderez P.; Sial, Alcides N.; Pimentel, Marcio M.; Armstrong, Richard; Guimarães, Ignez P.; da Silva Filho, Adejardo F.; de Lima, Mariucha Maria C.; da Silva, Thyego R.

    2015-09-01

    The 572 Ma Guarany stock consists of magmatic epidote-bearing hornblende monzodiorite to biotite granite that intruded Paleoproterozoic orthogneisses about 10 km inland from the coast in northeastern Brazil. Co-magmatic diorite enclaves and dikes are abundant throughout the pluton. The monzodiorite-granite pluton and diorite enclaves are shoshonitic and display continuous trends in variation diagrams. They display chemical and isotopic characteristics of crustal melts, such as enrichment in incompatible elements, high back-calculated initial 87Sr/86Sr ratios (avg. 0.71253), negative εNd (0.57Ga) values (avg. - 14.58), as well as high and variable (+ 9.1 to + 11.1‰VSMOW) δ18O (zircon) values. Correlations between O-isotope and whole-rock silica contents, as well as initial 87Sr/86Sr ratios with 1/Sr concentrations, suggest hybridization of a lower continental crustal melt with more felsic crustal rocks, concomitant with fractional crystallization. Amphibole chemistry and whole rock Zr, TiO2 and P2O5 contents suggest magma solidification at a pressure ~ 7 kbar and near liquidus temperature ~ 900 °C. The parental magma was likely formed by partial melting of old (tDM = 2.0 Ga) amphibolitic lower continental crustal rocks, in a post-collisional setting, probably triggered by underplating of mantle-derived mafic magma during the period of relaxation after collision.

  3. 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

  4. Strontium Isotopic Variations in the Koolau Volcanic Series, Oahu, Hawaii: Results from KSDP Drill Core

    NASA Astrophysics Data System (ADS)

    Smith, M. M.; Depaolo, D. J.

    2005-12-01

    Surface samples of the Koolau tholeiite series, from the eastern side of the island of Oahu, Hawaii, have long been noted for their unusually high 87Sr/86Sr ratios (up to 0.7042) and other extreme geochemical parameters, as compared to both earlier and later Oahu lavas, values from other Hawaiian islands, and lavas from the Waianae volcano on west Oahu. It has been assumed that the geochemistry of the surface samples of Koolau applied to most of the volcano and that the extreme features were a relatively long-lived characteristic of the Hawaiian mantle plume at the time that the Koolau lavas were being erupted about 3 million years ago. The Koolau Scientific Drilling Project, which returned nearly continuous core from depths of 350 to 670 meters below sea level, provided an opportunity to probe deeper into the Koolau edifice (Haskins and Garcia, CMP, 147, 2004). We present new Sr isotope data on thirty whole rock samples from KSDP, which complement other isotopic data that have been reported recently (Salters and Blichert-Toft, submitted). The KSDP samples have variable, but generally significant, amounts of post-eruption weathering and hence the samples were strongly acid-leached before TIMS isotopic analysis in order to remove any seawater-derived strontium. The 87Sr/86Sr values in the core samples vary from values near 0.7040 at the top of the core to 0.7035 near the bottom. There is a general trend of increasing 87Sr/86Sr upsection as well as oscillations with peak-to-peak amplitude of 0.0003. The Sr isotope ratios correlate reasonably well with Nd and Hf isotope ratios. The data show that the Koolau surface samples are not representative of the volcano as a whole, and that the extreme geochemistry of the surface samples may represent only a minor component of the Hawaiian plume. The normal trend of Sr isotope ratios in the waning stages of shield building is from high values to low (as in Mauna Kea, Kohala, East Molokai and Haleakala). A trend toward higher

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

    NASA Astrophysics Data System (ADS)

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

    2004-11-01

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

  6. 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

  7. 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.

  8. 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.

  9. 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

  10. Strontium source and depth of uptake shifts with substrate age in semiarid ecosystems

    NASA Astrophysics Data System (ADS)

    Coble, Ashley A.; Hart, Stephen C.; Ketterer, Michael E.; Newman, Gregory S.; Kowler, Andrew L.

    2015-06-01

    Without exogenous rock-derived nutrient sources, terrestrial ecosystems may eventually regress or reach a terminal steady state, but the degree to which exogenous nutrient sources buffer or slow to a theoretical terminal steady state remains unclear. We used strontium isotope ratios (87Sr/86Sr) as a tracer and measured 87Sr/86Sr values in aeolian dust, soils, and vegetation across a well-constrained 3 Myr semiarid substrate age gradient to determine (1) whether the contribution of atmospheric sources of rock-derived nutrients to soil and vegetation pools varied with substrate age and (2) to determine if the depth of uptake varied with substrate age. We found that aeolian-derived nutrients became increasingly important, contributing as much as 71% to plant-available soil pools and tree (Pinus edulis) growth during the latter stages of ecosystem development in a semiarid climate. The depth of nutrient uptake increased on older substrates, demonstrating that trees in arid regions can acquire nutrients from greater depths as ecosystem development progresses presumably in response to nutrient depletion in the more weathered surface soils. Our results demonstrate that global and regional aeolian transport of nutrients to local ecosystems is a vital process for ecosystem development in arid regions. Furthermore, these aeolian nutrient inputs contribute to deep soil nutrient pools, which become increasingly important for maintaining plant productivity over long time scales.

  11. 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.

  12. 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.

  13. 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.

  14. Geochronology of archean gneisses in the Lake Helen area, Southwestern Big Horn Mountains, Wyoming

    USGS Publications Warehouse

    Arth, Joseph G.; Barker, F.; Stern, T.W.

    1980-01-01

    The RbSr and UPb methods were used to study gneisses in the 7 1 2-minute Lake Helen quadrangle of the Big Horn Mountains, Wyoming. Two episodes of magmatism, deformation and metamorphism occurred during the Archean. Trondhjemitic to tonalitic orthogneisses and amphibolite of the first episode (E-1) are cut by a trondhjemite pluton and a calc-alkaline intrusive series of the second episode (E-2). The E-2 series includes hornblende-biotite quartz diorite, biotite tonalite, biotite granodiorite and biotite granite. A RbSr whole-rock isochron for E-1 gneisses indicates an age of 3007 ?? 34 Ma (1 sigma) and an initial 87Sr/86Sr of 0.7001 ?? 0.0001. UPb determination on zircon from E-1 gneisses yield a concordia intercept age of 2947 ?? 50 Ma. The low initial ratio suggests that the gneisses had no significant crustal history prior to metamorphism, and that the magmas from which they formed had originated from a mafic source. A RbSr whole-rock isochron for E-2 gneisses gives an age of 2801 ?? 31 Ma. The 87Sr/86Sr initial ration is 0.7015 ?? 0.0002 and precludes the existence of the rocks for more than 150 Ma prior to metamorphism. The E-2 magmas may have originated from melting of E-1 gneisses or from a more mafic source. ?? 1980.

  15. 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.

  16. Sr isotopes as a tracer of weathering processes and dust inputs in a tropical granitoid watershed, Luquillo Mountains, Puerto Rico

    NASA Astrophysics Data System (ADS)

    Pett-Ridge, Julie C.; Derry, Louis A.; Kurtz, Andrew C.

    2009-01-01

    Sr isotope data from soils, water, and atmospheric inputs in a small tropical granitoid watershed in the Luquillo Mountains of Puerto Rico constrain soil mineral development, weathering fluxes, and atmospheric deposition. This study provides new information on pedogenic processes and geochemical fluxes that is not apparent in watershed mass balances based on major elements alone. 87Sr/ 86Sr data reveal that Saharan mineral aerosol dust contributes significantly to atmospheric inputs. Watershed-scale Sr isotope mass balance calculations indicate that the dust deposition flux for the watershed is 2100 ± 700 mg cm -2 ka -1. Nd isotope analyses of soil and saprolite samples provide independent evidence for the presence of Saharan dust in the regolith. Watershed-scale Sr isotope mass balance calculations are used to calculate the overall short-term chemical denudation velocity for the watershed, which agrees well with previous denudation rate estimates based on major element chemistry and cosmogenic nuclides. The dissolved streamwater Sr flux is dominated by weathering of plagioclase and hornblende and partial weathering of biotite in the saprock zone. A steep gradient in regolith porewater 87Sr/ 86Sr ratio with depth, from 0.70635 to as high as 0.71395, reflects the transition from primary mineral-derived Sr to a combination of residual biotite-derived Sr and atmospherically-derived Sr near the surface, and allows multiple origins of kaolinite to be identified.

  17. 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.

  18. Childhood lead exposure in an enslaved African community in Barbados: implications for birthplace and health status.

    PubMed

    Schroeder, Hannes; Shuler, Kristrina A; Chenery, Simon R

    2013-02-01

    Lead was ubiquitous on Caribbean sugar plantations, where it was used extensively in the production of sugar and rum. Previous studies suggest that skeletal lead contents can be used to identify African-born individuals (as opposed to Creoles) among slave burials found in the New World. To test this hypothesis, we measured lead concentrations in enamel samples from 26 individuals from the Newton Plantation cemetery in Barbados, which was in use from around 1660 to 1820, and compared the results with enamel (87) Sr/(86) Sr measurements that had been previously obtained for the same population. Results show a clear association between low (i.e., below 1 ppm) enamel lead concentrations and higher enamel (87) Sr/(86) Sr ratios which have previously been interpreted as being indicative of African birth, suggesting that individuals with low enamel lead levels were indeed born in Africa as opposed to the New World. Based on these results, we propose that enamel lead measurements provide an effective and inexpensive way to determine African birth from skeletal remains. Furthermore, the lead measurements can provide useful insights into the health status and childhood environment of enslaved Africans during the colonial period. PMID:23225156

  19. 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.

  20. Petrogenesis of peralkaline rhyolites in an intra-plate setting: Glass House Mountains, southeast Queensland, Australia

    NASA Astrophysics Data System (ADS)

    Shao, Fengli; Niu, Yaoling; Regelous, Marcel; Zhu, Di-Cheng

    2015-02-01

    We report petrological and geochemical data on coeval trachybasalts, syenites with enclaves, trachytes, peralkaline rhyolites and peraluminous rhyolites from the Glass House Mountains-Maleny-Noosa area, southeast Queensland, Australia. This rock association and the unique characteristics of the peralkaline rhyolites offer convincing lines of evidence that the petrogenesis of the peralkaline rhyolites is a straightforward consequence of protracted fractional crystallization from basaltic melts of alkali-rich composition. Compared to the common peraluminous rhyolites elsewhere, the peralkaline rhyolites here are characterized by elevated abundances of most incompatible elements, especially the very high Nb (vs. Th) and Ta (vs. U), the very low Ba, Sr and Eu and the extremely high 87Sr/86Sr ratio. The high Nb and Ta are inherited from the parental alkali basaltic melts. The low Ba, Sr and Eu result from removal of plagioclase during the protracted fractional crystallization. These rocks altogether define a Rb-Sr isochron of ~ 28 Ma, which is similar to Ar-Ar age data on these rocks in the literature. The extremely high 87Sr/86Sr ratio of the peralkaline rhyolites (up to 1.88) is actually characteristic of peralkaline rhyolites because of extreme Sr (also Eu and Ba) depletion and thus the very high Rb/Sr ratio. That is, the Sr in these rocks is essentially radiogenic 87Sr accumulated from the 87Rb decay since the volcanism. We suggest that the petrogenesis of the peralkaline rhyolites from the Glass House Mountain area may be of general significance globally. The coeval peraluminous rhyolites apparently result from crustal anatexis in response to the basaltic magma underplating. The small "Daly Gap" exhibited in this rock association is anticipated during the protracted fractional crystallization from basaltic parent to the more evolved felsic varieties.

  1. 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

  2. Channelling of hydrothermal fluids during the accretion and evolution of the upper oceanic crust: Sr isotope evidence from ODP Hole 1256D

    NASA Astrophysics Data System (ADS)

    Harris, Michelle; Coggon, Rosalind M.; Smith-Duque, Christopher E.; Cooper, Matthew J.; Milton, James A.; Teagle, Damon A. H.

    2015-04-01

    ODP Hole 1256D in the eastern equatorial Pacific is the first penetration of a complete section of fast spread ocean crust down to the dike-gabbro transition, and only the second borehole to sample in situ sheeted dikes after DSDP Hole 504B. Here a high spatial resolution record of whole rock and mineral strontium isotopic compositions from Site 1256 is combined with core observations and downhole wireline geophysical measurements to determine the extent of basalt-hydrothermal fluid reaction and to identify fluid pathways at different levels in the upper ocean crust. The volcanic sequence at Site 1256 is dominated by sheet and massive lava flows but the Sr isotope profile shows only limited exchange with seawater. However, the upper margins of two anomalously thick (>25 m) massive flow sequences are strongly hydrothermally altered with elevated Sr isotope ratios and appear to be conduits of lateral low-temperature off-axis fluid flow. Elsewhere in the lavas, high 87Sr/86Sr are restricted to breccia horizons. Mineralised hyaloclastic breccias in the Lava-Dike Transition are strongly altered to Mg-saponite, silica and pyrite, indicating alteration by mixed seawater and cooled hydrothermal fluids. In the Sheeted Dike Complex 87Sr/86Sr ratios are pervasively shifted towards hydrothermal fluid values (∼0.705). Dike chilled margins display secondary mineral assemblages formed during both axial recharge and discharge and have higher 87Sr/86Sr than dike cores, indicating preferential fluid flow along dike margins. Localised increases in 87Sr/86Sr in the Dike-Gabbro Transition indicates the channelling of fluids along the sub-horizontal intrusive boundaries of the 25 to 50 m-thick gabbroic intrusions, with only minor increases in 87Sr/86Sr within the cores of the gabbro bodies. When compared to the pillow lava-dominated section from Hole 504B, the Sr isotope measurements from Site 1256 suggest that the extent of hydrothermal circulation in the upper ocean crust may be

  3. Magma interaction processes in syn-extensional granitoids: The Tertiary Menderes Metamorphic Core Complex, western Turkey

    NASA Astrophysics Data System (ADS)

    Erkül, Sibel Tatar; Erkül, Fuat

    2012-06-01

    Western Turkey, which forms the eastern part of the Aegean region, was subjected to continental extension that led to formation of metamorphic core complexes and associated syn-extensional granitoids. This study deals with petrogenesis of the syn-extensional Early Miocene Alaçamdağ (AG) and Middle Miocene Salihli (SG) granitoids and associated mafic microgranular enclaves (MME) in order to better understand the time-progressive evolution of the mantle sources beneath the extended continental crust in western Turkey. AG and SG granitoids consist of undeformed and ductility deformed granitoids together with abundant MMEs. They are calc-alkaline to high-K calc-alkaline rocks that are metaluminous to slightly peraluminous. Mg# of AG host rocks is slightly lower than that of SG host rocks. AG host rocks have higher Na2O, Ba, Rb, Rb/La and lower Al2O3, CaO, MgO, TiO2, Zr/Y values than those of the SG host rocks. AG and SG host rocks differ from those of MMEs, with their lower Al2O3, CaO, MgO, Fe2O3, TiO2, Sr, V, Mg# and higher SiO2 values. MMEs are intermediate, corresponding to monzonite, monzodiorite (in AG) and diorite (in SG) compositions and are more mafic with respect to their host rocks. In the primitive mantle (PM) normalized trace element patterns, host rock and MME samples have similar trace element patterns. All of these rocks are enriched in large ion lithophile elements (LILEs, Cs, Rb, Ba, Th, K and Sr) and strongly depleted high field strength elements (HFSEs, Ta, Nb, P, Ti) compared to the primitive mantle. The isotope ratios of the syn-extensional AG and SG rocks display increasing radiogenic strontium and decreasing radiogenic neodymium. Isotopic values for the AG and SG host rocks and MME samples are 87Sr/86Sr (AG host) = 0.708835-0.710206 and ɛNd(t) (AG host) = (- 5.36 to - 7.36); 87Sr/86Sr (AG MME) = 0.709107-0.709801 and ɛNd(t) (AG MME) = - 5.36 to - 7.36; 87Sr/86Sr (AG MME)=0.709107-0.709801 and ɛNd(t) (AG MME)=-5.55 to -6.51; 87Sr/86Sr (SG

  4. 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

  5. Problems in obtaining precise and accurate Sr isotope analysis from geological materials using laser ablation MC-ICPMS

    PubMed Central

    van der Wagt, B.; Koornneef, J. M.; Davies, G. R.

    2007-01-01

    This paper reviews the problems encountered in eleven studies of Sr isotope analysis using laser ablation multicollector inductively coupled plasma mass spectrometry (LA-MC-ICPMS) in the period 1995–2006. This technique has been shown to have great potential, but the accuracy and precision are limited by: (1) large instrumental mass discrimination, (2) laser-induced isotopic and elemental fractionations and (3) molecular interferences. The most important isobaric interferences are Kr and Rb, whereas Ca dimer/argides and doubly charged rare earth elements (REE) are limited to sample materials which contain substantial amounts of these elements. With modern laser (193 nm) and MC-ICPMS equipment, minerals with >500 ppm Sr content can be analysed with a precision of better than 100 ppm and a spatial resolution (spot size) of approximately 100 μm. The LA MC-ICPMS analysis of 87Sr/86Sr of both carbonate material and plagioclase is successful in all reported studies, although the higher 84Sr/86Sr ratios do suggest in some cases an influence of Ca dimer and/or argides. High Rb/Sr (>0.01) materials have been successfully analysed by carefully measuring the 85Rb/87Rb in standard material and by applying the standard-sample bracketing method for accurate Rb corrections. However, published LA-MC-ICPMS data on clinopyroxene, apatite and sphene records differences when compared with 87Sr/86Sr measured by thermal ionisation mass spectrometry (TIMS) and solution MC-ICPMS. This suggests that further studies are required to ensure that the most optimal correction methods are applied for all isobaric interferences. PMID:18080118

  6. 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

  7. 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

  8. 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

  9. Evidence for two shield volcanoes exposed on the island of Kauai, Hawaii

    USGS Publications Warehouse

    Holcomb, R.T.; Reiners, P.W.; Nelson, B.K.; Sawyer, N.-L.E.

    1997-01-01

    The island of Kauai has always been interpreted as a single shield volcano, but lavas of previously correlated reversed-to-normal magnetic-polarity transitions on opposite sides of the island differ significantly in isotopic composition. Samples from west Kauai have 87Sr/86Sr 18.25; samples from east Kauai have 87Sr/86Sr > 0.7037, ??Nd ??? 6.14, and 206Pb/204Pb < 18.25. Available data suggest that a younger eastern shield grew on the collapsed flank of an older western one.

  10. Geochemical variability of the Yucatan basement: Constraints from crystalline clasts in Chicxulub impactites

    NASA Astrophysics Data System (ADS)

    Kettrup, B.; Deutsch, A.

    2003-07-01

    The 65 Ma old Chicxulub impact structure with a diameter of about 180 km is again in the focus of the geosciences because of the recently commenced drilling of the scientific well Yaxcopoil- 1. Chicxulub is buried beneath thick post-impact sediments, yet samples of basement lithologies in the drill cores provide a unique insight into age and composition of the crust beneath Yucatan. This study presents major element, Sr, and Nd isotope data for Chicxulub impact melt lithologies and clasts of basement lithologies in impact breccias from the PEMEX drill cores C-1 and Y-6, as well as data for ejecta material from the K/T boundaries at La Lajilla, Mexico, and Furlo, Italy. The impact melt lithologies have an andesitic composition with significantly varying contents of Al, Ca, and alkali elements. Their present day 87Sr/86Sr ratios cluster at about 0.7085, and 143Nd/144Nd ratios range from 0.5123 to 0.5125. Compared to the melt lithologies that stayed inside the crater, data for ejecta material show larger variations. The 87Sr/86Sr ratios range from 0.7081 for chloritized spherules from La Lajilla to 0.7151 for sanidine spherules from Furlo. The 143Nd/144Nd ratio is 0.5126 for La Lajilla and 0.5120 for the Furlo spherules. In an tCHUR(Nd)-tUR(Sr) diagram, the melt lithologies plot in a field delimited by Cretaceous platform sediments, various felsic lithic clasts and a newly found mafic fragment from a suevite. Granite, gneiss, and amphibolite have been identified among the fragments from crystalline basement gneiss. Their 87Sr/86Sr ratios range from 0.7084 to 0.7141, and their 143Nd/144Nd ratios range from 0.5121 to 0.5126. The TNdDM model ages vary from 0.7 to 1.4 Ga, pointing to different source terranes for these rocks. This leads us to believe that the geological evolution and the lithological composition of the Yucatàn basement is probably more complex than generally assumed, and Gondwanan as well as Laurentian crust may be present in the Yucatàn basement.

  11. Magmatic Degassing in the Crust Is Mantle Source Dependent

    NASA Astrophysics Data System (ADS)

    Burnard, P.

    2014-12-01

    The 4He/40Ar* ratio (where 40Ar* is 40Ar corrected for atmospheric contamination) is known to be sensitive to magmatic degassing due to the different solubilities of He and Ar in silicate melts: 4He/40Ar* increases in the residual liquids because Ar is less soluble than He and therefore degasses more rapidly. Conversely, lithophile isotope ratios and incompatible trace element ratios (87Sr/86Sr, 143Nd/144Nd, La/Sm etc) are specifically chosen as these are largely insensitive to magmatic processes, including degassing (as far as mid-ocean ridges are concerned) but rather trace mantle heterogeneities. It is astonishing therefore that correlations between 4He/40Ar* and lithophile isotope ratios (such as 87Sr/86Sr or 143Nd/144Nd) exist in South East Indian Ridge basalts and basaltic glasses [1]. These correlations appear to be the result of enhanced degassing of magmas produced from enriched mantle: enriched mantle probably has higher C contents relative to depleted mantle, therefore degassing of 'enriched' compositions will start at higher pressure and the proportion of volatiles lost will be greater than for 'depleted' lavas. The 4He/40Ar* ratio of the erupted products depends on the proportion of volatiles lost, therefore 4He/40Ar* is higher in lavas derived from enriched as opposed to depleted magmas. Naturally, enriched lavas are also distinct from depleted lavas in their lithophile isotopic composition (high 87Sr/86Sr, low 143Nd/144Nd) and thus the observed correlations between lithophile isotopes and degassing (4He/40Ar*) is created. A simple degassing model suggests that, in order to generate the correlated variability in Sr and Nd isotopes and 4He/40Ar*, the mantle C concentration likely varies by factor ~2 [1]. Thus it is possible to link mantle C variability - which is difficult to asses due to shallow level degassing - with Sr isotopic composition, which is very commonly measured in mid-ocean ridge basalts: Sr isotopes can be used as a proxy for mantle C

  12. 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

  13. 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

  14. 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

  15. 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

  16. 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

  17. Pyroxenite and peridotite xenoliths from Hexigten, Inner Mongolia: Insights into the Paleo-Asian Ocean subduction-related melt/fluid-peridotite interaction

    NASA Astrophysics Data System (ADS)

    Zou, Dongya; Liu, Yongsheng; Hu, Zhaochu; Gao, Shan; Zong, Keqing; Xu, Rong; Deng, Lixu; He, Detao; Gao, Changgui

    2014-09-01

    The in situ major, trace-element and Sr-isotopic compositions of the peridotite and pyroxenite xenoliths from the Hexigten region in the Xing-Meng orogenic belt (XMOB) were examined to evaluate the influences and contributions of the Paleo-Asian Oceanic slab subduction on the lithospheric mantle transformation. Pyroxenes in the Type 1 pyroxenite exhibit low and variable Mg# (67-85) and relatively high 87Sr/86Sr ratios (0.7036-0.7053), indicating that they were formed by assimilation and fractional crystallization processes during a basaltic underplating event. The peridotite and Type 2 pyroxenite xenoliths sampled the lithospheric mantle and recorded subduction-related metasomatism. The mineral chemistries of the Type 1 peridotite suggest that the lithospheric mantle beneath this area suffered 1-15% melt extraction. Clinopyroxene (Cpx) in some Type 1 peridotites are characterized by high (La/Yb)N coupled with marked depletions in high field strength elements (HFSE) (Nb, Ta, Zr, Hf and Ti) and negative correlations between the low Ti/Eu (Nb/La) and 87Sr/86Sr ratios (0.7037-0.7055), suggesting metasomatism by subduction-related CO2-rich fluids. Olivine (Ol) and orthopyroxene (Opx) in the Type 2 peridotite are characterized by a relatively low Mg# but high Ni contents. In addition to the normal incompatible element-depleted Opx, Opx with enrichments in Rb, Ba, Th, U, Nb, Ta and LREE were observed, as well. The Mg# of incompatible element-depleted Opx exhibits weak zonations (i.e., decreasing from the cores to the rims). Cpx and Opx of the Type 2 pyroxenite exhibit similarly high Mg# and Ni contents. Rb, Ba, Th, U, Nb, Ta and LREE contents and 87Sr/86Sr ratios of the Cpx increase from the cores to the rims. Moreover, Opx in the Type 2 peridotite and Cpx in the Type 2 pyroxenite exhibit increased Nb/Ta ratios and Ni contents relative to those in the Type 1 peridotites. These observations collectively suggest a rutile-bearing eclogite-derived silicic melt

  18. 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

  19. 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. PMID:23136452

  20. Stable isotopes of lead and strontium as tracers of sources of airborne particulate matter in Kyrgyzstan

    NASA Astrophysics Data System (ADS)

    Dewan, Nitika; Majestic, Brian J.; Ketterer, Michael E.; Miller-Schulze, Justin P.; Shafer, Martin M.; Schauer, James J.; Solomon, Paul A.; Artamonova, Maria; Chen, Boris B.; Imashev, Sanjar A.; Carmichael, Greg R.

    2015-11-01

    Central Asia is dominated by an arid climate and desert-like conditions, leading to the potential for long-range transport of desert dust within and out of the region. Of particular interest is the Aral Sea, which has receded in size largely due to water diversion. As a result, newly exposed sediments are resuspended by wind and thus, may be a potential new source of particulate matter within the region. Here, strontium and lead stable isotope ratios are employed along with detailed elemental composition, to explore the contribution of long-range transport of Aral Sea sediments, as well as other potential sources of dust, within Central Asia. Ambient PM10 samples were collected during dust and non-dust events from mid-2008 to mid-2009 at two sites in Kyrgyzstan located ˜1200 and 1500 km ESE of the Aral Sea. Aral Sea sediments and local Kyrgyzstan soils were resuspended and sized to PM10. The Aral Sea sediments have an average 87Sr/86Sr ratio of 0.70992. In contrast, the Sr isotope ratio in local soils exhibits an average ratio of 0.71579. Ambient PM10 collected in Kyrgyzstan has an average 87Sr/86Sr ratio of 0.71177, falling between the values of these two potential sources and indicating a complex mixture of contributing sources. At both sites, airborne Sr isotope ratios measured during dust events were similar, suggesting that Aral Sea sediments only minimally affect air quality in Kyrgyzstan. Elemental analysis and Pb isotope ratios supported this finding. While the Pb isotopes and elemental data both indicate an anthropogenic source, long-range dust transport from other deserts inside and outside the region cannot be ruled out as sources of PM10 in Central Asia.

  1. 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

  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. 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

  4. 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

  5. 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

  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. Rare earth elements, S and Sr isotopes and origin of barite from Bahariya Oasis, Egypt: Implication for the origin of host iron ores

    NASA Astrophysics Data System (ADS)

    Baioumy, Hassan M.

    2015-06-01

    Based on their occurrences and relation to the host iron ores, barites are classified into: (1) fragmented barite occurs as pebble to sand-size white to yellowish white barite along the unconformity between the Bahariya Formation and iron ores, (2) interstitial barite is present as pockets and lenses of large and pure crystals inside the iron ores interstitial barite inside the iron ores, and (3) disseminated barite occurs at the top of the iron ores of relatively large crystals of barite embedded in hematite and goethite matrix. In the current study, these barites have been analyzed for their rare earth elements (REE) as well as strontium and sulfur isotopes to assess their source and origin as well as the origin of host iron ores. Barite samples from the three types are characterized by low ΣREE contents ranging between 12 and 21 ppm. Disseminated barite shows relatively lower ΣREE contents (12 ppm) compared to the fragmented (19 ppm) and interstitial (21 ppm) barites. This is probably due to the relatively higher Fe2O3 in the disseminated barite that might dilute its ΣREE content. Chondrite-normalized REE patterns for the three barite mineralizations exhibit enrichment of light rare earth elements (LREE) relative to heavy rare earth elements (HREE) as shown by the high (La/Yb)N ratios that range between 14 and 45 as well as pronounced negative Ce anomalies varying between 0.03 and 0.18. The 87Sr/86Sr ratios in the analyzed samples vary between 0.707422 and 0.712237. These 87Sr/86Sr values are higher than the 87Sr/86Sr ratios of the seawater at the time of barite formation (Middle Eocene with 87Sr/86Sr ratios of 0.70773 to 0.70778) suggesting a contribution of hydrothermal fluid of high Sr isotope ratios. The δ34S values in the analyzed barites range between 14.39‰ and 18.92‰. The lower δ34S ratios in the studied barites compared with those of the seawater at the time of barite formation (Middle Eocene with δ34S ratios of 20-22‰) is attributed to a

  8. 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

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

    NASA Astrophysics Data System (ADS)

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

    2011-05-01

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

  12. Compositions of HIMU, EM1, and EM2 from global trends between radiogenic isotopes and major elements in ocean island basalts

    NASA Astrophysics Data System (ADS)

    Jackson, Matthew G.; Dasgupta, Rajdeep

    2008-11-01

    Sr and Pb isotopes exhibit global trends with the concentrations of major elements (SiO 2, TiO 2, FeO, Al 2O 3 and K 2O) and major elements ratios (CaO/Al 2O 3 and K 2O/TiO 2) in the shield-stage lavas from 18 oceanic hotspots (including Hawaii, Iceland, Galapagos, Cook-Australs, St. Helena, Cape Verde, Cameroon, Canary, Madeira, Comoros, Azores, Samoa, Society, Marquesas, Mascarene, Kerguelen, Pitcairn, and Selvagen). Based on the relationships between major elements and isotopes in ocean island basalts (OIBs), we find that the lavas derived from the mantle end members, HIMU (or high 'μ' = 238U/ 204Pb), EM1 (enriched mantle 1), EM2 (enriched mantle 2), and DMM (depleted MORB [mid-ocean ridge basalt] mantle) exhibit distinct major element characteristics: When compared to oceanic hotspots globally, the hotspots with a HIMU (radiogenic Pb-isotopes and low 87Sr/ 86Sr) component, such as St. Helena and Cook-Australs, exhibit high CaO/Al 2O 3, FeO T, and TiO 2 and low SiO 2 and Al 2O 3. EM1 (enriched mantle 1; intermediate 87Sr/ 86Sr and low 206Pb/ 204Pb; sampled by hotspots like Pitcairn and Kerguelen) and EM2 (enriched mantle 2; high 87Sr/ 86Sr and intermediate 206Pb/ 204Pb; sampled by hotspots like Samoa and Societies) exhibit higher K 2O concentrations and K 2O/TiO 2 weight ratios than HIMU lavas. EM1 lavas exhibit the lowest CaO/Al 2O 3 in the OIB dataset, and this sets EM1 apart from EM2. A plot of CaO/Al 2O 3 vs K 2O/TiO 2 perfectly resolves the four mantle end member lavas. Melting processes (pressure, temperature and degree of melting) fail to provide an explanation for the full spectrum of major element concentrations in OIBs. Such processes also fail to explain the correlations between major elements and radiogenic isotopes. Instead, a long, time integrated history of various parent-daughter elements appears to be coupled to major element and/or volatile heterogeneity in the mantle source. End member lava compositions are compared with experimental partial

  13. Origin of silicic magma in Iceland revealed by Th isotopes

    SciTech Connect

    Sigmarsson, O.; Condomines, M. ); Hemond, C. ); Fourcade, S. ); Oskarsson, N. )

    1991-06-01

    Th, Sr, Nd, and O isotopes have been determined in a suite of volcanic rocks from Hekla and in a few samples from Askja and Krafla volcanic centers in Iceland. Although {sup 87}Sr/{sup 86}Sr and {sup 143}Nd/{sup 144}Nd ratios are nearly the same for all compositions at Hekla, the ({sup 230}Th/{sup 232}Th) ratios differ and thus clearly show that the silicic rocks cannot be derived from fractional crystallization of a more primitive magma. Similar results are obtained for the Krafla and Askja volcanic centers, where the {delta}{sup 18}O values are much lower in the silicic magma than in the mafic magma. These data suggest that large volumes of silicic rocks in central volcanoes of the neovolcanic zones in Iceland are produced by partial melting of the underlying crust.

  14. 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.

  15. 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.

  16. Uranium from German Nuclear Power Projects of the 1940s--A Nuclear Forensic Investigation.

    PubMed

    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

    2015-11-01

    Here we present a nuclear forensic study of uranium from German nuclear projects which used different geometries of metallic uranium fuel. Through measurement of the (230)Th/(234)U 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 (87)Sr/(86)Sr ratio were measured. The results provide evidence that the uranium was mined in the Czech Republic. Trace amounts of (236)U and (239)Pu 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

  17. 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

  18. Sr, Nd, and Pb isotopic character of Tertiary basalts from southwest Poland

    NASA Astrophysics Data System (ADS)

    Blusztajn, Jerzy; Hart, Stanley R.

    1989-10-01

    Tertiary basaltic volcanics from southwest Poland which form the eastern part of the Central European Volcanic Province (CEVP) have been studied for Sr, Nd, and Pb isotopic compositions. 87Sr/86Sr ratios range from 0.70317 to 0.70369, 143Nd/144Nd ratios range from 0.51285 to 0.51302 and Pb isotopic compositions range from 19.42 to 19.94 for 206Pb/204Pb. These data indicate the influence of three end-member mantle components DMM, HIMU and EM. An analysis of all isotopic results from the CEVP leads to the conclusion that basalts from SW Poland have the most depleted character. We propose a model whereby the depleted source mantle for the CEVP interacted with enriched components (EM). The western part of the CEVP was enriched on a larger scale than the eastern part, probably due to the influence of the Rhine Graben rift.

  19. 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

  20. Sr isotope diversity of hot spring and volcanic lake waters from Zao volcano, Japan

    NASA Astrophysics Data System (ADS)

    Ishikawa, Hiromasa; Ohba, Tsukasa; Fujimaki, Hirokazu

    2007-09-01

    The ratio of 87Sr/ 86Sr was measured from different water samples of thermal/mineral (hot spring as well as crater lake) and meteoric origins, in order to specify the location and to verify the detailed model of a volcano-hydrothermal system beneath Zao volcano. The ratio showed a trimodal distribution for the case of thermal/mineral water: 0.7052-0.7053 (Type A, Zao hot spring), 0.7039-0.7043 (Type B, Okama crater lake and Shin-funkiko hot spring), and 0.7070-0.7073 (Type C, Gaga, Aone, and Togatta hot springs), respectively. However, in comparison, the ratio was found to be higher for meteoric waters (0.7077-0.7079). The water from the central volcanic edifice (Type B) was found to be similar to that of nearby volcanic rocks in their Sr isotopic ratio. This indicates that the Sr in water was derived from shallow volcanic rocks. The 87Sr/ 86Sr ratio for water from the Zao hot spring (Type A) was intermediate between those of the pre-Tertiary granitic and the Quaternary volcanic rocks, thus suggesting that the water had reacted with both volcanic and granitic rocks. The location of the vapor-liquid separation was determined as the boundary of the pre-Tertiary granitic and the Quaternary volcanic rocks by comparing the results of this strontium isotopic study with those of Kiyosu and Kurahashi [Kiyosu, Y., Kurahashi, M., 1984. Isotopic geochemistry of acid thermal waters and volcanic gases from Zao volcano in Japan. J. Volcanol. Geotherm. Res. 21, 313-331.].

  1. Recycled oceanic crust and marine sediment in the source of alkali basalts in Shandong, eastern China: Evidence from magma water content and oxygen isotopes

    NASA Astrophysics Data System (ADS)

    Liu, Jia; Xia, Qun-Ke; Deloule, Etienne; Chen, Huan; Feng, Min

    2015-12-01

    The magma water contents and cpx δ18O values in alkali basalts from the Fuyanyshan (FYS) volcano in Shandong, eastern China, were investigated by an inverse calculation based on the water content of clinopyroxene (cpx) phenocrysts, the ivAlcpx-dependent water partitioning coefficient Dwatercpx>/melt, and secondary ion mass spectrometer, respectively. The calculated water content (H2O wt.) of magma ranges from 0.58% to 3.89%. It positively correlates with heavy rare earth element concentrations and bulk rock 87Sr/86Sr ratios, and it negatively correlates with Nb/U ratios. However, it is not correlated with bulk Mg# (Mg# = 100 × Mg / (Mg + Fe)) and (La/Yb)n (n represents primitive mantle normalization). Combined with the rather homogenous distribution of water content within cpx grains, these correlations indicate that the water variations among different samples represent the original magma signature, rather than results of a shallow process, such as degassing and diffusion. The δ18O of cpx phenocrysts varies from 3.6‰ to 6.3‰ (±0.5‰, 2SD), which may be best explained by the involvement of components from the lower and upper oceanic crust with marine sediments within the mantle source. The H2O/Ce ratios of the calculated melts range from 113 to 696 and form a positive trend with bulk rock 87Sr/86Sr, which cannot be explained by the recycled Sulu eclogite or by the metasomatized lithospheric mantle. Our modeling calculation shows that the decoupling of ɛHf and ɛNd could be caused by the involvement of marine sediments. Combing the high Ba/Th ratios, positive Sr spikes, and low Ce/Pb ratios for the Fuyanshan basalts, we suggest that the hydrous nature of the FYS basalts was derived from the hydrous mantle transition zone with ancient sediments.

  2. 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.

  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. 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

  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. 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.

  7. 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.

  8. 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

  9. 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

  10. Magma chamber dynamics constrained by crystal isotope stratigraphy

    NASA Astrophysics Data System (ADS)

    Davidson, J. P.; Tepley, F. J., III; Hora, J. M.

    2003-04-01

    The architecture of subvolcanic magma plumbing systems controls the thermal regime transited by magmas in the lithosphere, and consequently influences the rates and processes by which magmas evolve. The resolution of current geophysical methods is unable to accurately define the shapes, sizes and crystallinity of small magma bodies. Exhumed fossil magma chambers may provide terminal or cumulative plumbing system assemblies but cannot provide snapshots of the system at a given time, and fail to identify ephemeral components such as dikes, which may open and close to transport magma. Petrographically-constrained in situ analysis of the components of volcanic rocks, including crystal isotope stratigraphy, has recently proved an important new approach to constraining the dynamics of magma storage systems. Core-to-rim decreases in 87Sr/86Sr accompanied by increases in Sr concentration for single plagioclase crystals seen at volcanoes such as El Chichon, Mexico, are explained by frequent recharge of a storage reservoir(s). The fact that high 87Sr/86Sr values are restricted to cores suggests that contamination occurs at the initial stages of injection and contact between magma and the crust. This in turn suggests that crystallization occurs at the margins of the magma body where the thermal gradient is strongest, volatiles are concentrated and epitaxial crystallization is promoted. The crystallized boundary zone then isolates the magma and prevents subsequent recharge magma from interacting directly with the crust. In cases such as Ngauruhoe volcano, New Zealand, 87Sr/86Sr increases from core-to-rim of plagioclase crystals suggest that the magma was not completely isolated from a crustal contaminant. In either case, changes in Sr isotope ratio are correlated with punctuated textural evidence for disequilibrium events, underscoring the importance of recharge. Recharge disaggregates and remobilizes much of the material crystallized from earlier events. Petrographic and

  11. Andesites/Dacites of the Oceanic Narcondam Volcano, Andaman Sea: Modification of Tholeiitic Arc Basalts by Crustal Contamination and Amphibole-Dominated Fractionation

    NASA Astrophysics Data System (ADS)

    Gillam, A. N.; Streck, M. J.; Ramos, F. C.; Bindeman, I. N.; Hart, G. L.

    2008-12-01

    The active Barren Island volcano and its 140 km distant northern neighbor, the Pleistocene Narcondam volcano, are the only two subaerially exposed arc volcanoes, which rise from the 1000-2300 m deep seafloor of the Andaman Sea, that result of the subduction of the Indian plate beneath the Burma plate. Lavas of Barren Island volcano range from basalt to andesite while lavas from Narcondam volcano range from andesite to silicic andesite/dacite. Similarities in the geochemistry of both lava suites include strong and comparable depletion in Nb and Ta (K2O/Nb ~0.7; Ba/Nb 130-250); low, MORB-like Nb/Zr (0.01- 0.03); and nearly constant U/Th (0.15-0.22). These characteristics suggest a genetic link between both magma suites. Distinct geochemical differences, however, include isotopic ratios which for Barren Island are: 87Sr/86Sr ~0.7039-0.7041, 143Nd/144Nd 0.51285-0.51296, and δ18O plagioclase 5.81-5.89, and for Narcondam are: 87Sr/86Sr 0.7049-0.7053, 143Nd/144Nd ~0.51270, and δ18O plagioclase 6.78-7.44. Other geochemical parameters (e.g. Sr/Y, Th/La, U/La, Ba/La) of Narcondam lavas positively correlate with increasing SiO2 but are anchored at the mafic end within compositions observed at Barren Island volcano. Narcondam magmas evolved through a multi-stage evolution characterized by fractional crystallization, contamination, and magma mixing. Prior to eruption, the latest event was marked by mixing of a silicic lava with a Barren Island-type basaltic magma that lowered the 87Sr/86Sr from values of 0.7053-0.7054 as observed in single plagioclase and amphibole phenocrysts to values of bulk rock and caused juxtaposition of mineral populations. The generally more-incompatible trace element enriched silicic Narcondam magmas are best explained by amphibole-dominated fractionation of a Barren Island-type basalt; being consistent with an increase of Sr/Y with increased silica of samples containing abundant amphibole. The shift in isotopic values from Barren Island to Narcondam

  12. Stable isotope systematics in mesozoic granites of Central and Northern California and Southwestern Oregon

    USGS Publications Warehouse

    Masi, U.; O'Neil, J.R.; Kistler, R.W.

    1981-01-01

    18O, D, and H2O+ contents were measured for whole-rock specimens of granitoid rocks from 131 localitics in California and southwestern Oregon. With 41 new determinations in the Klamath Mountains and Sierra Nevada, initial strontium isotope ratios are known for 104 of these samples. Large variations in ??18O (5.5 to 12.4), ??D (-130 to -31), water contents (0.14 to 2.23 weight percent) and initial strontium isotope ratios (0.7028 to 0.7095) suggest a variety of source materials and identify rocks modified by secondary processes. Regular patterns of variation in each isotopic ratio exist over large geographical regions, but correlations between the ratios are generally absent except in restricted areas. For example, the regular decrease in ??D values from west to east in the Sierra Nevada batholith is not correlative with a quite complex pattern of ??18O values, implying that different processes were responsible for the isotopic variations in these two elements. In marked contrast to a good correlation between (87Sr/86Sr)o and ??18O observed in the Peninsular Ranges batholith to the south, such correlations are lacking except in a few areas. ??D values, on the other hand, correlate well with rock types, chemistry, and (87Sr/86Sr)o except in the Coast Ranges where few of the isotopic signatures are primary. The uniformly low ??D values of samples from the Mojave Desert indicate that meteoric water contributed much of the hydrogen to the rocks in that area. Even so, the ??18O values and 18O fractionations between quartz and feldspar are normal in these same rocks. This reconnaissance study has identified regularities in geochemical parameters over enormous geographical regions. These patterns are not well understood but merit more detailed examination because they contain information critical to our understanding of the development of granitoid batholiths. ?? 1981 Springer-Verlag.

  13. Strontium and neodymium isotopic study of Libyan Desert Glass: Inherited Pan-African age signatures and new evidence for target material

    NASA Astrophysics Data System (ADS)

    Schaaf, P.; Müller-Sohnius, D. M.

    2002-04-01

    Libyan Desert Glass (LDG) is an impact-related, natural glass of still unknown target material. We have determined Rb-Sr and Sm-Nd isotopic ratios from seven LDG samples and five associated sandstones from the LDG strewn field in the Great Sand Sea, western Egypt. Planar deformation features were recently detected in quartz from these sandstones. 87Sr/86Sr ratios and e-Nd values for LDG range between 0.71219 and 0.71344, and between -16.6 and -17.8, respectively, and hence are distinct from the less radiogenic 87Sr/86Sr ratios of 0.70910-0.71053 and e-Nd values from -6.9 to -9.6 for the local sandstones from the LDG strewn field. Previously published isotopic ratios from the Libyan BP and Oasis crater sandstones are generally incompatible with our LDG values. LDG formation undoubtedly occurred at 29 Ma, but neither the Rb-Sr nor the Sm-Nd isotopic system were rehomogenised during the impact event, as we can deduce from Pan-African ages of ~540 Ma determined from the regression lines from a total of 14 LDG samples from this work and the literature. Together with similar Sr and Nd isotopic values for LDG and granitoid rocks from northeast Africa west of the Nile, these findings point to a sandy matrix target material for the LDG derived from a Precambrian crystalline basement, ruling out the Cretaceous sandstones of the former "Nubian Group" as possible precursors for LDG.

  14. Controls over the strontium isotope composition of river water

    NASA Astrophysics Data System (ADS)

    Palmer, M. R.; Edmond, J. M.

    1992-05-01

    Strontium concentrations and isotope ratios have been measured in river and ground waters from the Ganges, Orinoco, and Amazon river basins. When compared with major element concentrations, the data set has allowed a detailed examination of the controls over the strontium isotope systematics of riverine input to the oceans in the following environments: (1) "typical" drainage basins containing limestones, evaporites, shales, and alumino-silicate metamorphic and igneous rocks; (2) shield terrains containing no chemical or biogenic sediments; and (3) the floodplains that constitute the largest areas of many large rivers. The strontium concentration and isotope composition of river waters are largely defined by mixing of strontium derived from limestones and evaporites with strontium derived from silicate rocks. The strontium isotope composition of the limestone endmember generally lies within the Phanerozoic seawater range, which buffers the 87Sr /86Sr ratios of major rivers. A major exception is provided by the rivers draining the Himalayas, where widescale regional metamorphism appears to have led to an enrichment in limestones of radiogenic strontium derived from coexisting silicate rocks. The strontium isotope systematics of rivers draining shield areas are controlled by the intense, transportlimited, nature of the weathering reactions, and thereby limits variations in the strontium flux from these terrains. Floodplains are only a minor source of dissolved strontium to river waters, and precipitation of soil salts in some floodplains can reduce the riverine flux of dissolved strontium to the oceans. The most effective mechanisms for altering the isotope ratio and flux of riverine strontium to the oceans are increased glaciation and large-scale regional metamorphism of the type produced during continental collision. Both mechanisms provide a means for increasing the 87Sr /86Sr ratio of the global riverine flux.

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

    NASA Astrophysics Data System (ADS)

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

    1986-09-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2011-12-01

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

  17. Strontium Isotope Study of Coal Untilization By-products Interacting with Environmental Waters

    SciTech Connect

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

    2011-09-01

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

  18. Triple junction magmatism: a geochemical study of Neogene volcanic rocks in western California

    USGS Publications Warehouse

    Johnson, C.M.; O'Neil, J.R.

    1984-01-01

    Inception of volcanism at late Oligocene to Recent centers in the eastern Coast Ranges of California (ECR suite) regularly decreases in age northward and is correlated with the northward migration of the transform-transform-trench Mendocino triple junction (MTJ). Miocene volcanism in the southern California basin (SCB suite) is spatially and temporally associated with the transform-ridge-trench Rivera triple junction (RTJ). The tholeiitic to calc-alkaline rocks in both suites were erupted through older trench melange while arc magmatism was occurring several hundred kilometers to the east. Therefore they are not related to subduction zone magmatism, but instead to interactions of the MTJ and RTJ with the continental margin. The ECR rocks, dominantly intermediate to silicic in composition, have relatively high ??18O values up to 11.3, 87Sr 86Sr ratios up to 0.7055, as well as relatively high Th contents, suggesting that crustal anatexis played a dominant role in their generation. Coupled crystal fractionation and crustal assimilation by an initially basaltic magma cannot explain the high ??18O values and 87Sr 86Sr ratios because greater than 95% of the basalt would need to crystallize. In contrast, the SCB rocks, dominantly mafic to intermediate in composition, have relatively low ??18O values down to 5.2 and 87Sr 86Sr ratios down to 0.7025 suggesting that these rocks were derived dominantly from a mantle source. Whether crustal anatexis occurs is determined largely by the type of stress a triple junction imposes upon the continental margin. Both the MTJ and RTJ are associated with high heat flow and magma fluxes from the mantle. The transform-transform-trench MTJ is associated with locally variable mild extension to compression and therefore allows pooling of basaltic magma in the crust to initiate crustal melting. The high rates of continental extension associated with the transform-ridge-trench RTJ prevents such pooling of magma. The space created by decoupling

  19. Authentication of bell peppers using boron and strontium isotope compositions

    NASA Astrophysics Data System (ADS)

    Rosner, Martin; Pritzkow, Wolfgang; Vogl, Jochen; Voerkelius, Susanne

    2010-05-01

    The wrong declaration of food in terms of geographical origin and production method is a major problem for the individual consumer and public regulatory authorities. The authentication of food matrices using H-C-N-O-S isotopic compositions is already well established. However, specific questions require additional isotopic systems, which are more diagonstic for the source reservoires involved or production methods used. Here we present B and Sr isotopic compositions of bell peppers from Europe (Germany, Austria, Netherlands, Spain) and Israel to verfiy their origin. The bell peppers' B isotopic compositions between different locations are highly variable (d11BNISTSRM951 -8 to +35 ‰), whereas the 87Sr/86Sr ratios are all close to modern seawater Sr isotopic composition of about 0.7092 (0.7078 to 0.7107), but still can reliably be distinguished. Distinct isotopically heavy and light B isotopic fingerprints are obtained for bell peppers from Israel and the Netherlands. Samples from Germany, Austria, and Spain display overlapping d11B values between 0 and +12 ‰. Bell peppers from Israel show high d11B values (+28 to +35 ‰) combined with 87Sr/86Sr ratios slightly more unradiogenic than modern seawater (ca 0.7079). Bell peppers from the Netherlands, however, show low d11B values (-8 ‰) combinded with 87Sr/86Sr ratios of modern seawater (approx. 0.7085). Mainly based on diagnostic B isotopic compositions bell peppers from Israel and the Netherlands can be related to a specific geographical growing environment (Israel) or production method (Netherlands). The isotope fingerprints of bell peppers from the Netherlands are consistent with growing conditions in greenhouses typical for the Netherlands vegetable farming. Using optimized production methods crops in greenhouses were supplied with nutritients by liquid fertilizers on artificial substrates. As most fertilizers derive from non-marine salt deposits, fertilization typically imprints invariant d11B values close

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

    USGS Publications Warehouse

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

    2012-01-01

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

  1. Reconstruction of crustal blocks of California on the basis of initial strontium isotopic compositions of Mesozoic granitic rocks

    USGS Publications Warehouse

    Kistler, Ronald Wayne; Peterman, Zell E.

    1978-01-01

    Initial 87Sr/ 86 Sr was determined for samples of Mesozoic granitic rocks in the vicinity of the Garlock fault zone in California. These data along with similar data from the Sierra Nevada and along the San Andreas fault system permit a reconstruction of basement rocks offset by the Cenozoic lateral faulting along both the San Andreas and Garlock fault systems. The location of the line of initial 87Sr/ 86 Sr = 0.7060 can be related to the edge of the Precambrian continental crust in the western United States. Our model explains the present configuration of the edge of Precambrian continental crust as the result of two stages of rifting that occurred about 1,250 to 800 m.y. ago, during Belt sedimentation, and about 600 to 350 m.y. ago, prior to and during the development of the Cordilleran geosyncline and to left-lateral translation along a locus of disturbance identified in the central Mojave Desert. The variations in Rb, Sr, and initial 87Sr/ 86 Sr of the Mesozoic granitic rocks are interpreted as due to variations in composition and age of the source materials of the granitic rocks. The variations of Rb, Sr, and initial 87Sr/ 86 Sr in Mesozoic granitic rocks, the sedimentation history during the late Precambrian and Paleozoic, and the geographic position of loci of Mesozoic magmatism in the western United States are related to the development of the continental margin and different types of lithosphere during rifting.

  2. Strontium isotope geochemistry of calcite fracture fillings in deep core, Yucca Mountain, Nevada; A progress report

    SciTech Connect

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

    1992-11-01

    This paper reports on the variation of {sup 87}SR/{sup 86}Sr in calcite fracture fillings as a function of depth which has been determined using samples from five boreholes at Yucca Mountain. The data group into three discrete populations. Within 400 m of the present-day land surface, the distribution of {sup 87}Sr/{sup 86}Sr for calcite fracture fillings is similar to that of calcretes and near-surface veins suggesting an origin by infiltrating meteoric water. Veins within a 100-m zone immediately about the modern water table have {sup 87}Sr/{sup 86}Sr values similar to those of ground water from the Cenozoic volcanic aquifer suggesting a past connection between the two through aqueous diffusion or a higher water level. {sup 87}Sr/{sup 86}Sr values for calcite fracture fillings below the water table are low (mean = 0.70909 {plus_minus} 0.00038) and similar to those of the host rocks. The surficial calcites and those in the vadose zone are clearly unrelated to the deep calcite fracture fillings.

  3. Geochemistry of tholeiitic and alkalic lavas from the Koolau Range, Oahu, Hawaii: implications for Hawaiian volcanism

    USGS Publications Warehouse

    Roden, M.F.; Frey, F.A.; Clague, D.A.

    1984-01-01

    Lavas of the post-erosional, alkalic Honolulu Volcanics have significantly lower 87Sr 86Sr and higher 143Nd 144Nd than the older and underlying Koolau tholeiites which form the Koolau shield of eastern Oahu, Hawaii. Despite significant compositional variation within lavas forming the Honolulu Volcanics, these lavas are isotopically (Sr, Nd, Pb) very similar which contrasts with the isotopic heterogeneity of the Koolau tholeiites. Among Hawaiian tholeiitic suites, the Koolau lavas are geochemically distinct because of their lower iron contents and Sr and Nd isotopic ratios which range to bulk earth values. These geochemical data preclude simple models such as derivation of the Honolulu Volcanics and Koolau tholeiites from a common source by different degrees of melting or by mixing of two geochemically distinct sources. There may be no genetic relationship between the origin and evolution of these two lava suites; however, the trend shown by Koolau Range lavas of increasing 143Nd 144Nd and decreasing 87Sr 86Sr with decreasing eruption age and increasing alkalinity also occurs at Haleakala, East Molokai and Kauai volcanoes. A complex mixing model proposed for Haleakala lavas can account for the variations in Sr and Nd isotopic ratios and incompatible element abundances found in lavas from the Koolau Range. This model may reflect mixing and melting processes occurring during ascent of relatively enriched mantle through relatively depleted MORB-related lithosphere. Although two isotopically distinct components may be sufficient to explain Sr and Nd isotopic variations at individual Hawaiian volcanoes, more than two isotopically distinct materials are required to explain variations of Sr, Nd and Pb isotopic ratios in all Hawaiian lavas. ?? 1984.

  4. Petrogenesis of Late Cenozoic volcanic rocks from the Raton-Clayton volcanic field, northeastern New Mexico and southeastern Colorado

    SciTech Connect

    Zhu, J.; Stormer, J.C.; Wright, J.E. . Dept. of Geology and Geophysics); Middlefeldt, D.D. )

    1993-04-01

    The Raton-Clayton volcanic field, located in the eastern flank of the Rio Grande rift on the Great Plains, is at the northeastern end of the Jemez lineament. A broad variety of late Cenozoic volcanic rocks ranging from rhyodacites through basalts to basanites and nephelinites, with well established ages, provides a good probe of magma sources at different depths down to the mantle. New Sr, Nd and Pb isotopic data on late Cenozoic volcanic rocks from the Raton-Clayton volcanic field yield significant variations. [sup 87]Sr/[sup 86]Sr ratios vary from 0.70397--0.70499, [var epsilon][sub Nd] values range from [minus]3.7--2.4, [sup 206]Pb/[sup 204]Pb ratios are in the range of 17.43--18.48, [sup 207]Pb/[sup 204]Pb from 15.45--15.54 and [sup 208]Pb/[sup 204]Pb from 37.27--38.05. The mafic feldspathoidal rocks, believed to be derived from the enriched mantle reservoir with little crustal contamination, show relatively homogeneous [sup 87]Sr/[sup 86]Sr (ca. 0.7041) and [var epsilon][sub Nd] (ca. 2). A positive trend of Pb isotopic ratios, however, suggests possible mantle heterogeneity in Pb isotopic composition beneath the continent. Isotopic data from basaltic lavas display well defined variation trends, bringing to light the role of crustal components in the magmatic process. A strong signature of upper crustal involvement is indicated in the formation of tholeiitic basalts with dicktytaxitic texture, while isotope data from alkali olivine basalts and Capulin trachybasalts suggest lower crust contaminations of these rocks. An apparent isotopic variation trend of the dicktytaxitic basalts is well correlated with geographic location from south to north. Significant discrepancies in isotopic compositions of more silicic rocks compared with those of similar rocks from the Taos Plateau volcanic field to the west, may indicate either large differences in lower crustal composition or different mechanisms in generating these magmas.

  5. Sr isotope signatures of Austrian trees as a tool for the determination of origin of prehistoric wood

    NASA Astrophysics Data System (ADS)

    Horsky, Monika; Tintner, Johannes; Grabner, Michael; Kowarik, Kerstin; Reschreiter, Hans; Kern, Anton; Prohaska, Thomas

    2013-04-01

    Wood artefacts from prehistoric times have been preserved in a salt mine environment in Hallstatt, Austria, for more than 3000 years and thus present a unique archive of information on past mining industry. Certain findings are assumed to have been traded, so the finding spot is not equivalent to the growth region of the tree. Therefore, 87Sr/86Sr isotope ratio measurements have been applied to investigate the origin of these artefacts, in order to allow conclusions on trade routes. As a basis for this, modern trees from several selected regions in Austria were analysed for their Sr isotopic ratios. The regions were chosen based on archaeological knowledge of settlements in the time period of interest and under consideration of the geological, climatic and silvicultural situation. Four tree species, which are also represented in the archaeological finds, were sampled. Thus, the first steps towards a map of Sr isotopic signatures bioavailable to different trees in Austria are presented here. The applicability to the prehistoric findings, however, is challenged by the storage conditions with respect to inorganic contamination by the repository material. The extent of penetration of salt into the wood tissue was screened using laser ablation ICPMS. A decontamination strategy based on acid leaching was developed and successful separation of contamination and natural strontium could be achieved. This was shown by measurement of 87Sr/86Sr in leaching solutions and digests of wood using multi-collector ICPMS. The assumption of non-exhaustive removal of secondary salts was included into the evaluation by adoption of a mixing curve, which allows the mathematical extraction of biogenic Sr isotope ratios of the wood samples.

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  7. Petrogenesis of the magmatic complex at Mount Ascutney, Vermont, USA - I. Assimilation of crust by mafic magmas based on Sr and O isotopic and major element relationships

    USGS Publications Warehouse

    Foland, K.A.; Henderson, C.M.B.; Gleason, J.

    1985-01-01

    The Ascutney Mountain igneous complex in eastern Vermont, USA, is composed of three principal units with compositions ranging from gabbro to granite. Sr and O isotopic and major element relationships for mafic rocks, granites, and nearby gneissic and schistose country rock have been investigated in order to describe the petrogenesis of the mafic suite which ranges from gabbro to diorite. The entire complex appears to have been formed within a short interval 122.2??1.2 m.y. ago. The granites with ??18O near +7.8??? had an initial 87Sr/86Sr of 0.70395(??6) which is indistinguishable from the initial ratio of the most primitive gabbro. Initial 87Sr/86Sr ratios and ??18O values for the mafic rocks range from 0.7039 to 0.7057 and +6.1 to +8.6???, respectively. The isotopic ratios are highly correlated with major element trends and reflect considerable crustal contamination of a mantle-derived basaltic parent magma. The likely contaminant was Precambrian gneiss similar to exposed bedrock into which the basic rocks were emplaced. A new approach to modelling of assimilation during the formation of a cogenetic igneous rock suite is illustrated. Chemical and isotopic modelling indicate that the mafic rocks were produced by simultaneous assimilation and fractional crystallization. The relative amounts of fractionation and assimilation varied considerably. The mafic suite was not produced by a single batch of magma undergoing progressive contamination; rather, the various rocks probably were derived from separate batches of magma each of which followed a separate course of evolution. The late stage granite was apparently derived from basaltic magma by fractionation with little or no crustal assimilation. The early intrusive phases are much more highly contaminated than the final one. The observed relationships have important implications for the formation of comagmatic complexes and for isotopic modelling of crustal contamination. ?? 1985 Springer-Verlag.

  8. Combining metal and nonmetal isotopic measurements in barite to identify mode of formation

    NASA Astrophysics Data System (ADS)

    Griffith, E. M.; Paytan, A.; Eisenhauer, A.; Scher, H. D.; Wortmann, U.

    2014-12-01

    Barite (BaSO4) is a highly stable and widely-distributed mineral found in magmatic, metamorphic, and sedimentary rocks (of all ages), as well as in soils, aerosol dust, and extraterrestrial material. Today, barite can form in a variety of settings in the oceans (hydrothermal, cold seeps, water column, sediments) and on the continents - where supersaturation and precipitation of barite typically occurs from the mixing of fluids - one containing Ba and another containing sulfate. Sulfur (δ34S) and oxygen (δ18O) isotopes together with 87Sr/86Sr and stable Sr-isotopic signatures (δ88/86Sr) of modern authigenic continental barite are compared to modern pelagic marine barite and marine hydrothermal and cold seep barite to investigate the potential for their combined use to indicate mode of barite formation. The 87Sr/86Sr in barite cleary identifies the source of fluid for any particular type of barite (as previously noted, see Paytan et al., 2002). The highest (most radiogenic) 87Sr/86Sr values are measured in continental barite samples. There is no unique δ88/86Sr signature for any particular type of barite, but coretop marine (pelagic) barite has a consistent value measured from samples collected in different ocean basins. The highest and lowest δ88/86Sr values were measured in continental barite samples. The combination of isotopic systems result in unique δ88/86Sr and δ18O relationships and distinct δ88/86Sr and δ34S relationships for different types of barites investigated. Data suggest that the combined use of these metal and nonmetal isotopic measurements in barite could be useful as a new geochemical proxy to identify mode of barite mineralization for use in earth science applications including understanding ancient barite deposits.

  9. Isotopes as tracers of the Hawaiian coffee-producing regions.

    PubMed

    Rodrigues, Carla; Brunner, Marion; Steiman, Shawn; Bowen, Gabriel J; Nogueira, José M F; Gautz, Loren; Prohaska, Thomas; Máguas, Cristina

    2011-09-28

    Green coffee bean isotopes have been used to trace the effects of different climatic and geological characteristics associated with the Hawaii islands. Isotope ratio mass spectrometry (IRMS) and inductively coupled plasma mass spectrometry ((MC)-ICP-SFMS and ICP-QMS) were applied to determine the isotopic composition of carbon (δ13C), nitrogen (δ15N), sulfur (δ34S), and oxygen (δ18O), the isotope abundance of strontium (87Sr/86Sr), and the concentrations of 30 different elements in 47 green coffees. The coffees were produced in five Hawaii regions: Hawaii, Kauai, Maui, Molokai, and Oahu. Results indicate that coffee plant seed isotopes reflect interactions between the coffee plant and the local environment. Accordingly, the obtained analytical fingerprinting could be used to discriminate between the different Hawaii regions studied. PMID:21838232

  10. Nd and Sr isotope systematics of Shombole volcano, East Africa, and the links between nephelinites, phonolites, and carbonatites

    SciTech Connect

    Bell, K. ); Peterson, T. )

    1991-06-01

    Nd and Sr isotope compositions of nephelinites, carbonatites, and phonolites from Shombole, a Pliocene volcano in East Africa, show that the phonolites cannot be derived by simple fractional crystallization of nephelinite magma. For a given initial {sup 87}Sr/{sup 86}Sr ratio, {sup 143}Nd/{sup 144}Nd is lower in most phonolites than in the nephelinites and carbonatites. Interaction between nephelinitic magma and lower-crustal granulites can account for these differences. The similar ranges in isotopic composition of the carbonatites and nephelinites are consistent with repeated melting events involving heterogeneous mantle. The carbonatites could have formed by immiscibility with nephelinite magma or by direct partial melting of the same mantle source(s) as the nephelinites.

  11. Leachates formed carbonates in ALH84001 and on early Mars

    NASA Astrophysics Data System (ADS)

    Melwani Daswani, M.; Grady, M. M.; Schwenzer, S. P.; Wright, I. P.

    2013-09-01

    Evidence abounds for liquid water existing on Mars prior to the late heavy bombardment (LHB) ~3.9 Ga ago and physicochemically interacting with rocks to form distinct geomorphological landforms and mineralogical alteration products (e.g. [3, 4, 8, 14]). ALH84001, the oldest (~4.5-4.1 Ga [11, 13]) known martian meteorite, contains secondary carbonate minerals formed on Mars ~3.9-4.0 Ga ago [5], roughly contemporaneous to the LHB. Recent isotopic evidence supports their formation at low temperature (~18 °C [9]) and also by fluids derived from aqueous weathering in the Noachian/Phyllosian, due to the elevated 87Sr/86Sr ratios in the carbonates and bulk rock of ALH84001 [1].

  12. Isotopes as Tracers of the Hawaiian Coffee-Producing Regions

    PubMed Central

    2011-01-01

    Green coffee bean isotopes have been used to trace the effects of different climatic and geological characteristics associated with the Hawaii islands. Isotope ratio mass spectrometry (IRMS) and inductively coupled plasma mass spectrometry ((MC)-ICP-SFMS and ICP-QMS) were applied to determine the isotopic composition of carbon (δ13C), nitrogen (δ15N), sulfur (δ34S), and oxygen (δ18O), the isotope abundance of strontium (87Sr/86Sr), and the concentrations of 30 different elements in 47 green coffees. The coffees were produced in five Hawaii regions: Hawaii, Kauai, Maui, Molokai, and Oahu. Results indicate that coffee plant seed isotopes reflect interactions between the coffee plant and the local environment. Accordingly, the obtained analytical fingerprinting could be used to discriminate between the different Hawaii regions studied. PMID:21838232

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

    USGS Publications Warehouse

    Clague, D.A.

    1982-01-01

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

  14. Isotopic Composition of the Neolithic Alpine Iceman's Tooth Enamel and Clues to his Origin

    NASA Astrophysics Data System (ADS)

    Muller, W.; Muller, W.; Halliday, A. N.

    2001-12-01

    -related disturbance. Enamel fragments from three teeth are characterized by virtually similar and high 87Sr/^{86}Sr ratios of 0.7203-0.7206, consistent with the compositions of crystalline gneisses and schists close to the finding site. Sites overlying bedrock built up by limestone from further south or north can clearly be excluded as the Iceman's childhood area. Among the three teeth, enamel mineralized approximately during a 2-3 year interval starting with the canine at the age of ~2 years. Hence, during this period, the food source for the Iceman must have remained essentially constant. Two compact bone samples from the damaged hip region have 87Sr/^{86}Sr ratios of 0.7175 and 0.7181, significantly lower than that of the enamel. The internal variation in the Iceman's bone Sr isotopic composition argues for somewhat different Sr turnover times within the skeleton, but it is evident that during the last 1-3 decades of his life, food from a different region was utilized. The 87Sr/^{86}Sr ratios of the initial bone leachates point towards post-mortem alteration with water having 87Sr/^{86}Sr ratios higher than ~0.718, consistent with that measured for contemporaneous ice samples (0.720-0.723). These Sr isotopic variations among ice samples may have implications for the post depositional (climate) history of the Iceman's finding site, since it appears unlikely that substantial compositional differences among adjacent ice samples would be preserved if the site had thawed near completely during e.g. the Roman warm period.

  15. Isotope sourcing of prehistoric willow and tule textiles recovered from western Great Basin rock shelters and caves - proof of concept

    USGS Publications Warehouse

    Benson, L.V.; Hattori, E.M.; Taylor, H.E.; Poulson, S.R.; Jolie, E.A.

    2006-01-01

    Isotope and trace-metal analyses were used to determine the origin of plants used to manufacture prehistoric textiles (basketry and matting) from archaeological sites in the western Great Basin. Research focused on strontium (87Sr/86Sr) and oxygen (18O/16O) isotope ratios of willow (Salix sp.) and tule (Schoenoplectus sp.), the dominant raw materials in Great Basin textiles. The oxygen-isotope data indicated that the willow and tule used to produce the textiles were harvested from the banks of rivers or in marshes characterized by flowing water and not from lakes or sinks. The strontium-isotope data were useful in showing which plants came from the Humboldt River and which came from rivers headed in the Sierra Nevada.

  16. Primitive and contaminated basalts from the Southern Rocky Mountains, U.S.A

    USGS Publications Warehouse

    Doe, B.R.; Lipman, P.W.; Hedge, C.E.; Kurasawa, H.

    1969-01-01

    Basalts in the Southern Rocky Mountains province have been analyzed to determine if any of them are primitive. Alkali plagioclase xenocrysts armored with calcic plagioclase seem to be the best petrographic indicator of contamination. The next best indicator of contamination is quartz xenocrysts armored with clinopyroxene. On the rocks and the region studied, K2O apparently is the only major element with promise of separating primitive basalt from contaminated basalt inasmuch as it constitutes more than 1 % in all the obviously contaminated basalts. K2O: lead (> 4 ppm) and thorium (> 2 ppm) contents and Rb/Sr (> 0.035) are the most indicative of the trace elements studied. Using these criteria, three basalt samples are primitive (although one contains 1.7% K2O) and are similar in traceelement contents to Hawaiian and Eastern Honshu, Japan, primitive basalts. Contamination causes lead isotope ratios, 206Pb/204Pb and 208Pb/204Pb, to become less radiogenic, but it has little or no effect on 87Sr/86Sr. We interpret the effect on lead isotopes to be due to assimilation either of lower crustal granitic rocks, which contain 5-10 times as much lead as basalt and which have been low in U/Pb and Th/Pb since Precambrian times, or of upper crustal Precambrian or Paleozoic rocks, which have lost much of their radiogenic lead because of heating prior to assimilation. The lack of definite effects on strontium isotopes may be due to the lesser strontium contents of granitic crustal rocks relative to basaltic rocks coupled with lack of a large radiogenic enrichment in the crustal rocks. Lead isotope ratios were found to be less radiogenic in plagioclase separates from an obviously contaminated basalt than in the primitive basalts. The feldspar separate that is rich in sodic plagioclase xenocrysts was found to be similar to the whole-rock composition for 206Pb/204Pb and 208Pb/204Pb whereas a more dense fraction probably enriched in more calcic plagioclase phenocrysts is more similar

  17. Mid-Paleozoic age of granitoids in enclaves within early Cretaceous granulites, Fiordland, southwest New Zealand

    USGS Publications Warehouse

    Bradshaw, J.Y.; Kimbrough, D.L.

    1991-01-01

    Orthogneisses of granite, quartz monzonite, monzonite, and tonalite, occur locally as isolated enclaves within the Early Cretaceous granulite terrain (Western Fiordland Orthogneiss - WFO). Discordant U-Pb zircon isotopic data (seven fractions) from four granitoid samples from enclaves at George Sound, define an upper intecept age of 341??34 Ma that is interpreted as approximating the time of formation of the granitoid suite. The lower intercept age of 93??37 Ma is interpreted as approximating the time of zircon isotopic disturbance by major episodic Pb loss. The low 87Sr/ 86Sr initial ratio indicates that these mid-Paleozoic granitoids were derived from an isotopically primitive source. The granitoid enclaves within WFO show influences of several different sources. The granitoids provide evidence linking WFO to a mid-Palaeozoic country rock similar to the central Fiordland metasediments. -from Authors

  18. U-Pb zircon dates of morin anorthosite suite rocks, Grenville Province, Quebec

    SciTech Connect

    Doig, R. )

    1991-09-01

    U-Pb zircon ages of samples of anorthosite, pyroxene monzodiorite (jotunite), and pyroxene quartz monzonite (quartz mangerite) of the Morin anorthosite complex, Grenville Province, Quebec, are 1155 {plus minus} 3, 1146 {plus minus} 4 and 1135 {plus minus} 3 Ma, respectively. These dates are very similar to available dates for equivalent units of the Lac St-Jean and Adirondack anorthosite suite occurrences and slightly predate estimates of 1075-1100 Ma for peak metamorphic conditions during the Grenville orogeny in this region. {sup 87}Sr/{sup 86}Sr initial ratios of 0.7048-0.7051 for the three Morin units sampled permit a comagmatic origin if the different emplacement or cooling times can be reconciled. The mangerite sampled cannot have been formed by fusion of the upper crust, but may have been derived from a relatively juvenile crust at depth. All three units have interacted with continental crust, given the likely depleted nature of the mantle in this region.

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

    USGS Publications Warehouse

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

    2007-01-01

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

  20. Chemical weathering of a soil chronosequence on granitoid alluvium: II. Mineralogic and isotopic constraints on the behavior of strontium

    USGS Publications Warehouse

    Bullen, T.; White, A.; Blum, A.; Harden, J.; Schulz, M.

    1997-01-01

    The use of strontium isotopes to evaluate mineral weathering and identify sources of base cations in catchment waters requires an understanding of the behavior of Sr in the soil environment as a function of time. Our approach is to model the temporal evolution of 87Sr/86Sr of the cation exchange pool in a soil chronosequence developed on alluvium derived from central Sierra Nevada granitoids during the past 3 Ma. With increasing soil age, 87Sr/86Sr of ammonium-acetate extractable Sr initially decreases from values typical of K-feldspar to those of plagioclase and hornblende and then remains constant, even though plagioclase and hornblende are absent from the soils after approximately 1 Ma of weathering. The temporal variation of 87Sr/86Sr of exchangeable Sr is modeled by progressively equilibrating Sr derived from mineral weathering and atmospheric deposition with Sr on exchange sites as waters infiltrate a soil column. Observed decreases in quartz-normalized modal abundances of plagioclase, hornblende, and K-feldspar with time, and the distinct 87Sr/86Sr values of these minerals can be used to calculate Sr flux from weathering reactions. Hydrobiotites in the soils have nearly constant modal abundances, chemistry, and 87Sr/86Sr over the chronosequence and provide negligible Sr input to weathering solutions. The model requires time and soil horizon-dependent changes in the amount of exchangeable Sr and the efficiency of Sr exchange, as well as a biologic cycling term. The model predicts that exchangeable Sr initially has 87Sr/86Sr identical to that of K-feldspar, and thus could be dominated by Sr leached from K-feldspar following deposition of the alluvium. The maximum value of 87Sr/86Sr observed in dilute stream waters associated with granitoids of the Yosemite region is likewise similar to that of the K-feldspars, suggesting that K-feldspar and not biotite may be the dominant source of radiogenic Sr in the streams. This study reveals that, when attempting to use

  1. Effects of urbanization on groundwater evolution in an urbanizing watershed

    NASA Astrophysics Data System (ADS)

    Reyes, D.; Banner, J. L.; Bendik, N.

    2011-12-01

    The Jollyville Plateau Salamander (Eurycea tonkawae), a candidate species for listing under the Endangered Species Act, is endemic to springs and caves within the Bull Creek Watershed of Austin, Texas. Rapid urbanization endangers known populations of this salamander. Conservation strategies lack information on the extent of groundwater contamination from anthropogenic sources in this karst watershed. Spring water was analyzed for strontium (Sr) isotopes and major ions from sites classified as "urban" or "rural" based on impervious cover estimates. Previous studies have shown that the 87Sr/86Sr value of municipal water is significantly higher than values for natural streamwater, which are similar to those for the Cretaceous limestone bedrock of the region's watersheds. We investigate the application of this relationship to understanding the effects of urbanization on groundwater quality. The use of Sr isotopes as hydrochemical tracers is complemented by major ion concentrations, specifically the dominant ions in natural groundwater (Ca and HCO3) and the ions associated with the addition of wastewater (Na and Cl). To identify high priority salamander-inhabited springs for water quality remediation, we explore the processes controlling the chemical evolution of groundwater such as municipal water inputs, groundwater-soil interactions, and solution/dissolution reactions. 87Sr/86Sr values for water samples from within the watershed range from 0.70760 to 0.70875, the highest values corresponding to sites located in the urbanized areas of the watershed. Analyses of the covariation of Sr isotopes with major ion concentrations help elucidate controls on spring water evolution. Springs located in rural portions of the watershed have low 87Sr/86Sr, high concentrations of Ca and HCO3, and low concentrations of Na and Cl. This is consistent with small inputs of municipal water. Three springs located in urban portions of the watershed have high 87Sr/86Sr, low Ca and HCO3, and

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

    SciTech Connect

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

    2007-08-07

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

  3. Petrochemistry of igneous rocks of the California-Vetas mining district, Santander, Colombia: Implications for northern Andean tectonics and porphyry Cu (-Mo, Au) metallogeny

    NASA Astrophysics Data System (ADS)

    Bissig, Thomas; Mantilla Figueroa, Luis Carlos; Hart, Craig J. R.

    2014-07-01

    Porphyry Mo and Cu mineralization in the California-Vetas mining district is contemporaneous with 10.9 to 8.4 Ma granodiorite porphyry stocks and overprinted by Au-Ag mineralization of epithermal affinity. Mineralization is hosted by Grenvillian aged paragneisses (Bucaramanga Gneiss of the Santander Massif) and late Triassic to early Jurassic granitic rocks. All intrusive rocks are high-K calc-alkaline. Late Triassic to early Jurassic rocks include peraluminous granites with more than 70 wt.% SiO2 as well as metaluminous diorites, tonalites and granodiorites with SiO2 between 54.9 and 60.4 wt.%. Late Miocene rocks are weakly peraluminous granodiorite porphyries with SiO2 between 61 and 67 wt.% SiO2. Late Miocene rocks share some characteristics with adakite-like rocks which are widely associated with porphyry and epithermal style mineralization elsewhere in the Andes. They have high Ba (930 to 1500 ppm) and high Ba/La (28 to 50), high Sr (850 to 1100 ppm) and Sr/Y (48-78) and depleted middle rare earth elements (MREE) compared to the Mesozoic granites, which have 400 to 700 ppm Ba (Ba/La 14 to 25) and 80 to 150 ppm Sr (Sr/Y 2.5 to 14), and Mesozoic diorites and tonalites, which have ~ 900 to 1200 ppm Ba (Ba/La 20 to 32) and ~ 610 to 750 ppm Sr (Sr/Y 22 to 25). Miocene granodiorite porphyries, in contrast to Mesozoic intrusive rocks have only weak negative Eu anomalies. The Miocene rocks have 87Sr/86Sr ratios of 0.7052 to 0.7067 and εNd of - 1.9 to - 5.4 and are significantly more isotopically primitive than all other rocks in the study area including the Mesozoic diorites to tonalites (87Sr/86Sr = 0.7082 and 0.7092; εNd = - 6.7 and - 7.2), granites (87Sr/86Sr = 0.730 (n = 2); εNd = - 8.2 and - 8.3) and Bucaramanga Gneiss (0.718 to 0.743; εNd = - 10.8 to - 14.1). Lead isotope data are broadly consistent with the Sr and Nd isotope data and the Miocene porphyries have the lowest 207Pb/204Pb ratios but overlap with the Mesozoic diorites to tonalites in their 206Pb

  4. The Halmahera Island Arc, Molucca Sea collision zone, Indonesia: A geochemical survey

    NASA Astrophysics Data System (ADS)

    Morris, J. D.; Jezek, P. A.; Hart, S. R.; Hill, J. B.

    The Halmahera island arc, northeastern Indonesia, is the east flank of the Molucca Sea collision zone which is the site of an active arc-arc collision. One unique aspect of the arc is the vast thickness of marine sediments outboard of the trench, a result of ˜1000-1500 km of closure in the Molucca Sea basin. The Halmahera arc is underlain by a 45° east dipping Benioff zone, which is present to depths of 230 km. The volcanoes form a single front which lies ˜100 km above the top of the slab. The arc can be separated into three regions, on the basis of tectonic setting and chemistry. Most volcanoes are part of the normal calc-alkaline oceanic arc segment. Lavas here are basalts through dacites, with basaltic andesites and andesites dominant. Suites are medium-K and show little to moderate Fe enrichment. Abundances of Al2O3, the alkali elements, compatible elements, and the high field strength elements are typical of calc-alkaline island arc lavas. 87Sr/86Sr ratios are 0.70357-0.70438 the average value for all volcanic centers is almost the same, but most centers show a large range of real variation around that average. Pb isotopic compositions are 206Pb/204Pb = 18.55-18.62, 207Pb/204 = Pb 15.55-15.63, 208Pb/204Pb = 38.48-38.67. On a Pb-Pb diagram, they form a linear cluster of steep slope, between oceanic sediments and the less radiogenic end of the mantle array. Pb and Sr isotopic compositions for the oceanic segment can be used to test models for the origin of arc lavas. Both isotope systems can be satisfied by a three-component mixing model where normal oceanic island basalt-type magma is mixed with MORB and contaminated by heterogeneous sediments. A two-component model, where OIB-type magmas (which are heterogeneous with respect to both Sr contents and 87Sr/86Sr ratios) are contaminated with sediments, can also explain the data. This generates isotopically heterogeneous suites, and much of this heterogeneity is preserved through the eruption process. A

  5. Magmatic interactions as recorded in plagioclase phenocrysts of Chaos Crags, Lassen Volcanic Center, California

    USGS Publications Warehouse

    Tepley, F. J., III; Davidson, J.P.; Clynne, M.A.

    1999-01-01

    The silicic lava domes of Chaos Crags in Lassen Volcanic National Park contain a suite of variably quenched, hybrid basaltic andesite magmatic inclusions. The inclusions represent thorough mixing between rhyodacite and basalt recharge liquids accompanied by some mechanical disaggregation of the inclusions resulting in crystals mixing into the rhyodacite host preserved by quenching on dome emplacement. 87Sr/86Sr ratios (~0.7037-0.7038) of the inclusions are distinctly lower than those of the host rhyodacite (~0.704-0.7041), which are used to fingerprint the origin of mineral components and to monitor the mixing and mingling process. Chemical, isotopic, and textural characteristics indicate that the inclusions are hybrid magmas formed from the mixing and undercooling of recharge basaltic magma with rhyodacitic magma. All the host magma phenocrysts (biotite, plagioclase, hornblende and quartz crystals) also occur in the inclusions, where they are rimmed by reaction products. Compositional and strontium isotopic data from cores of unresorbed plagioclase crystals in the host rhyodacite, partially resorbed plagioclase crystals enclosed within basaltic andesite inclusions, and partially resorbed plagioclase crystals in the rhyodacitic host are all similar. Rim 87Sr/86Sr ratios of the partially resorbed plagioclase crystals in both inclusions and host are lower and close to those of the whole-rock hybrid basaltic andesite values. This observation indicates that some crystals originally crystallized in the silicic host, were partially resorbed and subsequently overgrown in the hybrid basaltic andesite magma, and then some of these partially resorbed plagioclase crystals were recycled back into the host rhyodacite. Textural evidence, in the form of sieve zones and major dissolution boundaries of the resorbed plagioclase crystals, indicates immersion of crystals into a hotter, more calcic magma. The occurrence of partially resorbed plagioclase together with plagioclase

  6. The Hurd Peak gneiss of the Long Lake shear zone, eastern Sierra Nevada, California

    SciTech Connect

    Holland, K.S.; Reed, W.E. . Dept. of Earth and Space Sciences)

    1993-04-01

    The Hurd Peak gneiss is located within the Long Lake valley of the east-central Sierra Nevada, California. This unit is the principle orthogneiss in Hathaway's (1993) Long Lake shear zone. The rock shows porphyroclasts of plagioclase and quartz, abundant mafic enclaves, and cross-cutting field associations which suggest that the gneiss had a plutonic protolith. The gneiss varies from biotite-poor nearest the contact with the Lamarck to biotite-rich nearest Long Lake. The contact zone between the gneiss and the Lamarck pluton ranges from sharp to gradational and from migmatitic to mixed, i.e., the mixed zone being greater than 50% intermingled dikes of 10 cm or greater thickness. In places this contact is marked by a quartz-free biotite hornfels approximately 5 m thick. Based on their relative deformation, at least 3 suites of aplite dikes cross-cut the gneiss, and 5 other lithologies, including basaltic, mixed, composite, andesitic, and quartz dioritic compositions, also cross-cut the gneiss. The Rb-Sr whole rock isochron age of the Hurd Peak gneiss has been determined to be 90.2 Ma. The authors interpret this isochron to be the result of mobilization of the Rb-Sr isotopic system during intrusion of the Lamarck Granodiorite (90 Ma); this may represent a regional cooling age. The initial [sup 87]/Sr[sup 86]Sr ratio of the gneiss is 0.7098, i.e., much more evolved than the surrounding plutons which have [sup 87]Sr/[sup 86]Sr ratios near 0.706. Sr model ages indicate that the protolith of the gneiss is considerably older than 90 Ma, one such calculation suggests an age of approximately 250 Ma. Single crystals of zircon have been isolated from the gneiss for U-Pb dating, and analytical work on the zircons is presently on-going.

  7. Rb-Sr and oxygen isotopic study of alkalic rocks from the Trans-Pecos magmatic province, Texas: Implications for the petrogenesis and hydrothermal alteration of continental alkalic rocks

    SciTech Connect

    Lambert, D.D.; Malek, D.J.; Dahl, D.A. )

    1988-10-01

    Rb-Sr and O isotopic data for mid-Tertiary alkalic rocks from the Trans-Pecos magmatic province of west Texas demonstrate that hydrothermal alteration and fluid/rock (cation exchange) interactions have affected the isotope geochemistry of these rocks. Strontium and O isotopic data for late-stage minerals in an alkali basalt (hawaiite) still record two episodes of fluid/rock interactions. These data suggest that later meteoric fluids introduced Sr with a Cretaceous marine {sup 87}Sr/{sup 86}Sr ratio into minerals with significant cation exchange capacity. Dilute HCl leaching experiments demonstrate the removal of this labile or exchangeable Sr from the alkali basalt. Rb-Sr isotopic data for the leached alkali basalt and handpicked calcite record a crystallization age of 42 Ma, consistent with K-Ar data for an unaltered alkali basalt (hawaiite) dike from the same area (42.6 {plus minus} 1.3 Ma). Leaching experiments on one phonolite suggest the Sr isotopic variability in unleached phonolite and nepheline trachyte samples may be attributed to Sr in secondary calcite and zeolites, which have an upper Cretaceous marine {sup 87}Sr/{sup 86}Sr ratio. Rb-Sr isotopic data for leached phonolite and sanidine separate yield an age of 36.5 {plus minus} 0.8 Ma, within analytical uncertainty of a K-Ar biotite age (36.0 {plus minus} 1.1 Ma) of another phonolite. These leaching experiments demonstrate that the Rb-Sr isotopic systematics of hydrothermally-altered continental alkalic rocks may be significantly improved, providing more reliable geochronologic and isotopic tracer information necessary in constructing precise models of mantle sources.

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

    USGS Publications Warehouse

    Foland, K.A.; Friedman, I.

    1977-01-01

    The Red Hill ring complex in central New Hampshire is composed of apparently cogenetic syenites, nepheline-sodalite syenite, and granite. The ages and petrogenetic relations among five of the six recognized units have been investigated by rubidiumstrontium and oxygen isotope analysis of whole rocks and separated minerals. Whole-rock samples from three syenite units are consistent with a single Rb-Sr isochron which gives an age of 198??3 m.y. and an initial (87Sr/86Sr)o ratio of 0.70330??0.00016 (??2 sigma; ??=1.42?? 10-11y-1). However, Sr isotope data for two other units, nepheline syenite and granite, are not consistent with this isochron but rather indicate higher initial ratios which range from 0.7033 to about 0.707. Whole-rock O isotope analyses give ??18O values which range from+6.2 to+9.3??? Sr and O isotope analyses on mineral separates indicate that observed whole-rock variations in (87Sr/<