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1.
Kathrin Abraham Sophie Opfergelt François Fripiat Anne-Julie Cavagna Jeroen T.M. de Jong Stephen F. Foley Luc André Damien Cardinal 《Geostandards and Geoanalytical Research》2008,32(2):193-202
We report silicon isotopic determinations for USGS rock reference materials BHVO-1 and BHVO-2 using a Nu Plasma multi-collector (MC)-ICP-MS, upgraded with a new adjustable entrance slit, to obtain medium resolution, as well as a stronger primary pump and newly designed sampler and skimmer cones ("B" cones). These settings, combined with the use of collector slits, allowed a resolution to be reached that was sufficient to overcome the 14 N16 O and 14 N2 interferences overlying the 30 Si and the 28 Si peaks, respectively, in an earlier set-up. This enabled accurate measurement of both δ30 Si and δ29 Si. The δ value is expressed in per mil variation relative to the NBS 28 quartz reference material. Based on data acquired from numerous sessions spread over a period of six months, we propose a recommended average δ30 Si of −0.33 ± 0.05‰ and −0.29 ± 0.11‰ (2se) for BHVO-1 and BHVO-2, respectively. Our BHVO grand mean silicon isotope composition (δ30 Si =−0.31 ± 0.06‰) is significantly more negative than the only published value for BHVO-2, but is in very good agreement with the recently established average value of ocean island basalts (OIB), confirming the conclusion that the OIB reservoir has a distinct isotopic composition from the solar reservoir as sampled by chondrites. 相似文献
2.
Jean Carignan Nathalie Vigier Romain Millot 《Geostandards and Geoanalytical Research》2007,31(1):7-12
The CRPG (Nancy, France) has prepared secondary reference materials for Li isotope measurements by mixing 7 Li or 6 Li spikes and either L-SVEC or IRMM-016 certified reference materials to produce solutions having a known Li concentration and isotopic composition. The Li7-N and Li6-N solution samples (1.5 mol l−1 HNO3 ) have nominal δ7 Li isotopic compositions of 30.1‰ and -9.7‰ respectively relative to L-SVEC and concentrations of 100 mg l−1 . Repeated measurement of these samples using the QUAD-ICP-MS at the CRPG yielded δ7 Li of 30.4 ± 1.1‰ (n = 13) and -8.9 ± 0.9‰ (n = 9) at the 2s level of confidence. An additional LiCl-N solution was measured and yielded a delta value of 9.5 ± 0.6‰ (n = 3). Identical results were obtained at the BRGM (Orléans, France) from determinations performed with a Neptune MC-ICP-MS (30.2 ± 0.3‰, n = 89 for the Li7-N, -8.0 ± 0.3‰, n = 38 for the Li6-N and 10.1 ± 0.2‰, n = 46 for LiCl-N at the 2s level of confidence). The deviation of measured composition relative to the nominal value for the Li6-N solution might be explained by either contamination during preparation or an error during sample weighing. These secondary reference materials, previously passed through ion exchange resin or directly analysed, may be used for checking the accuracy of Li isotopic measurements over a range of almost 40‰ and will be available to the scientific community upon request to J. Carignan or N. Vigier, CRPG. 相似文献
3.
Stanislaw Halas Janina Szaran Maciej Czarnacki Ahmad Tanweer 《Geostandards and Geoanalytical Research》2007,31(1):61-68
Refinements have been made to achieve over 99% yield in the conversion of CO to CO2 in order to improve the reproducibility and accuracy of δ18 O measurements in sulfates. BaSO4 (10-15 mg) was mixed with an identical amount of spectrographic-grade graphite and loaded into a Pt boat. The mixture was gradually heated to 1100 °C to reduce sulfate to CO and CO2 ; the former gas was simultaneously converted to CO2 by a glow discharge between Pt electrodes immersed in a magnetic field (produced by a pair of external neodymium magnets). A small memory effect was noticed during the analysis (less than 0.3‰ per 10‰ difference in δ18 O between two subsequently analysed samples). The memory effect, however, was suppressed by repetitive preparation of the same specimen. CO2 produced in this way from sulfate reference samples was analysed on a dual inlet and triple collector mass spectrometer along with CO2 equilibrated with VSMOW, GISP and SLAP water reference samples. To avoid large departures of measured isotope ratios from 18 O/16 O of the working calibrator we used CO2 gas prepared from ocean water sulfate for this purpose. The calibrated δ18 O values (in ‰) obtained in this way for NBS-127, IAEA SO-5 and IAEA SO-6 reference materials were 8.73 ± 0.05, 12.20 ± 0.07 and -10.43 ± 0.12, respectively. 相似文献
4.
Ingrid Raczek Klaus Peter Jochum Albrecht W. Hofmann 《Geostandards and Geoanalytical Research》2003,27(2):173-179
We have measured 87 Sr/86 Sr and 14 3 Nd/14 4 Nd isotope ratios in different batches and aliquots of the new US Geological Survey (USGS) reference materials (RMs) BCR-2, BHVO-2, AGV-2 and GSP-2 and the original USGS RMs BCR-1, BHVO-1, AGV-1 and GSP-1 by thermal ionisation mass spectrometry. In addition, we also analysed the eight Max-Planck-Institut-Dingwell (MPI-DING) reference glasses. Nearly all isotope ratios obtained in the different aliquots and batches agree within uncertainty limits indicating excellent homogeneity of the USGS powders and the MPI-DING glasses. With the exception of GSP-2, the new USGS RMs are also indistinguishable from the ratios found in the original USGS RMs (87 Sr/86 Sr: 0.704960, 0.704958 (BCR-1, -2), 0.703436, 0.703435 (BHVO-1, -2), 0.703931, 0.703931 (AGV-1, -2); 14 3 Nd/14 4 Nd: 0.512629, 0.512633 (BCR-1, -2), 0.512957, 0.512957 (BHVO-1, -2); 0.512758, 0.512755 (AGV-1, -2)). This means that for normalisation purposes in Sr and Nd isotope geochemistry BCR-2, BHVO-2 and AGV-2 can well replace BCR-1, BHVO-1 and AGV-1 respectively. 相似文献
5.
Measurement of SIMS Instrumental Mass Fractionation of Pb Isotopes During Zircon Dating 总被引:8,自引:0,他引:8
Richard A. Stern Simon Bodorkos Sandra L. Kamo Arthur H. Hickman Fernando Corfu 《Geostandards and Geoanalytical Research》2009,33(2):145-168
An igneous zircon reference material (OG1) was characterised for U-Pb isotopes by ID-TIMS, and utilised to evaluate SIMS (SHRIMP) instrumental mass fractionation (IMF) of radiogenic Pb isotopes (207 Pb*/206 Pb*). The TIMS 207 Pb*/206 Pb* reference value for OG1 was 0.29907 ± 0.00011 (95% confidence limit), 3465.4 ± 0.6 Ma. The high 207 Pb* (∼ 30 μg g−1 ), negligible common Pb, and isotopic homogeneity permitted precise (± 1–2‰) 207 Pb*/206 Pb* measurements within the analytical sessions. External reproducibility of mean 207 Pb*/206 Pb* ratios between sessions was demonstrated for one instrument, yielding a mean IMF of +0.87 ± 0.49‰. The mean 207 Pb*/206 Pb* ratios between instruments were dispersed beyond uncertainties, with session IMF values from +3.6 ± 1.7‰ to −2.4 ± 1.3‰, and a grand mean IMF value (twenty-six sessions) of +0.70 ± 0.52‰, indicating a tendency towards elevated 207 Pb*/206 Pb*. The specific causes of variability in IMF are unclear, but generally reflect subtle differences in analytical conditions. The common practice in SIMS of assuming that IMF for Pb+ is insignificant could result in systematic age biases and underestimated uncertainties, of critical importance for precise correlation of Precambrian events. Nevertheless, a zircon RM such as OG1 can be readily incorporated into routine dating to improve 207 Pb*/206 Pb* accuracy and external reproducibility. 相似文献
6.
Stable isotopic and fluid inclusion evidence for meteoric fluid penetration into an active mountain belt; Alpine Schist, New Zealand 总被引:2,自引:0,他引:2
Calcite and quartz veins have formed, and are forming, in steeply dipping fissures in the actively rising Alpine Schist metamorphic belt of New Zealand. The fluids that deposited these minerals were mostly under hydrostatic pressure almost down to the brittle-ductile transition, which has been raised to 5-6 km depth by rapid uplift. Some fluids were trapped under lithostatic pressures. Fluids in the fissure veins were immiscible H2 O + NaCl-CO2 mixtures at 200-350 C. Bulk fluid composition is 15-20 mol% CO2 and <4.3 total mol CH4 + N2 + Ar/100mol H2 O. Water hydrogen isotopic ratio δDH2 O in the fissure veins spans -29 to -68‰, δ18 OH2 O -0.7 to 8.5‰, and bulk carbon isotopic ratio δ13 C ranges from -3.7 to -11.7‰. The oxygen and hydrogen isotopic data suggest that the water has a predominantly meteoric source, and has undergone an oxygen isotope shift as a result of interaction with the host metamorphic rock. Similar fluids were present during cooling and uplift. Dissolved carbon is not wholly derived from residual metamorphic fluids; part may be generated by oxidation of graphite. 相似文献
7.
Accurate and High-Precision Measurement of Lithium Isotopes in Two Reference Materials by MC-ICP-MS 总被引:5,自引:1,他引:5
Romain Millot Catherine Guerrot Nathalie Vigier 《Geostandards and Geoanalytical Research》2004,28(1):153-159
We report here a newly developed method for measurement of Li isotopes by use of multi-collector ICP-MS (Neptune) allowing rapid and high precision determination of Li isotope ratios at low levels of lithium (15–20 ng). The lithium reference sample solution IRMM-016 was analysed over a period of ten months with an external reproducibility of 0.24% (2s, n = 52). Chemical separation of Li from matrix was performed on the seawater sample IRMM BCR-403, for which a mean δ7 Li value of + 31.0 ± 0.1 % (2s/√n, n = 31) was obtained. This mean value is in good agreement with those previously published for other seawater samples. BCR-403 seawater being readily available, we propose that this seawater sample be used as a reference sample for Li isotope measurements. 相似文献
8.
Martin Rosner Lary Ball Bernhard Peucker-Ehrenbrink Jerzy Blusztajn Wolfgang Bach Jörg Erzinger 《Geostandards and Geoanalytical Research》2007,31(2):77-88
We report a new approach to conduct fast and accurate lithium isotope ratio measurements by MC-ICP mass spectrometry after wet chemical sample preparation. In contrast to most previously published methods our MC-ICP-MS set-up did not use a desolvating system to achieve appropriate ion beam intensities and, therefore, was less affected by matrix-induced shifts of the instrumental mass bias. As the total lithium background and build-up in the sample introduction system was low, previous sample residues could be washed out by an extended uptake of the new sample. Elimination of a nitric acid rinse step increased the sample throughput by a factor of two and allowed the instrumental mass bias drift to be tracked more precisely. δ7 Li values of powdered silicate rock reference materials and seawater obtained in this study revealed good accuracy and an overall analytical uncertainty of typically 0.5‰ (2s). On the basis of a comparison between our lithium isotope data and compiled literature data, we recommend preliminary average δ7 Li values for seawater (+30.8‰) and several silicate rock reference materials (BHVO-1: +5.0‰; JA-1: +5.6‰; JB-2: +4.8‰). The compilation of published δ7 Li values for seawater suggests that the observed large lithium isotope differences are due to inter-method and/or interlaboratory bias. Most recently published δ7 Li values for seawater show little variation and confirm a constant lithium isotope composition (at the sub ‰ level) of seawater in well mixed ocean basins. 相似文献
9.
Julie Prytulak Tim Elliott Dirk L. Hoffmann Christopher D. Coath 《Geostandards and Geoanalytical Research》2008,32(1):55-63
The accuracy of 231 Pa-235 U measurements can be readily assessed using a secular equilibrium reference material (RM), but a secular equilibrium RM is also required to calibrate the 233 Pa spike used in 231 Pa determinations. The only silicate RM commonly accepted to be in secular equilibrium is Table Mountain Latite (TML) and so an additional reference is required. Our measurements on the widely available USGS BCR-2 (Basalt Columbia River) rock powder yielded (231 Pa/235 U) = 0.997 ± 0.013 2s (n = 10), indicating its value as a secondary reference to test the fidelity of U-Pa determinations. Such a reference material additionally provides a useful check on data reduction, which our literature survey highlights can lead to discrepancies of up to 53% between reported (231 Pa/235 U) activity ratios and corresponding U and Pa concentration data. 相似文献
10.
J.C. de WIT C.M. van der STRAATEN W.G. MOOK 《Geostandards and Geoanalytical Research》1980,4(1):33-36
By mixing 1 H2 O and 2 H2 O, both with accurately known purity, samples were prepared with 2 H/1 H ratios close to those of the international isotopic water standards: V-SMOW and SLAP. A mass spectrometrical comparison of these calibration samples with the actual water standards revealed:
2 H/1 H of V-SMOW = (155.95 ± 0.08) × 10−6
2 H/1 H of SLAP = (89.12 ± 0.07) × 10−6
δ2 HV-SMOW (SLAP) =−428.5 ± 0.5 % 相似文献
δ
11.
ABSTRACT The Tripoli Formation (Lower Messinian) in Sicily includes diatomites irregularly alternating with marl and carbonate beds and lies, stratigraphically, between the Tortonian pelagic marls and the evaporitic Calcare di base. The relationships between mineralogy, textural features and oxygen-carbon isotopic compositions of carbonate components point to a wide variability of depositional conditions and suggest that Tripoli sedimentation occurred in small basins characterized by periodic and marked restriction from the open sea.
The isotopic values of calcite and dolomite in the diatomites suggest an evolution from normal marine towards more restricted environments. Evaporating conditions are also indicated by the occurrence of anhydrite, length-slow chalcedonic quartz and moulds of gypsum. In a more advanced stage, the precipitation of heavy δ18 0 dolomite in the interstitial pores of fossil-poor diatomites denotes an environment with highly evaporated water. Mixing of meteoric and marine waters, on the other hand, might have favoured the precipitation of a dolomite characterized by relatively low δ18 0 and δ13 C values.
The deposition of marl and carbonate beds alternating with or overlying the diatomites took place in an environment with highly evaporated marine waters on the basis of δl18 O values of dolomite (up to + 9.10‰) and aragonite (up to + 5.83‰), occurrence of evaporitic minerals and lack of fossils. The presence at these levels of calcite with extremely negative δ13 C values (down to - 38.40‰), filling gypsum moulds, suggests activity of sulphate-reducing bacteria. Some aragonitic marls, however, bear evidence of deposition in relatively normal marine conditions. 相似文献
The isotopic values of calcite and dolomite in the diatomites suggest an evolution from normal marine towards more restricted environments. Evaporating conditions are also indicated by the occurrence of anhydrite, length-slow chalcedonic quartz and moulds of gypsum. In a more advanced stage, the precipitation of heavy δ
The deposition of marl and carbonate beds alternating with or overlying the diatomites took place in an environment with highly evaporated marine waters on the basis of δl
12.
Routine trace-element geochemistry suggests that components in putative marine halite evaporites may be partly of nonmarine origin, but such interpretations are commonly ambiguous. Stable chlorine isotopes may provide a less-ambiguous marker of chloride origin where δ37 Cl departs from the range predicted for evaporite formation from seawater. Bedded halite with primary sedimentary textures preserves original δ37 Cl values. Measurable change in δ37 Cl can be generated by incongruent dissolution of halite, but only if less than half the original halite remains. Badenian (middle Miocene) halite from the Forecarpathian and from the East Slovakian and Transcarpathian basins has a δ37 Cl range of – 0.2 to 0.8‰. Two phenomena cannot be explained by simple evaporation of 0.0‰ seawater. At Wieliczka, the Shaft Salt has distinctive δ37 Cl values (– 0.2 to 0.0‰) relative to neighbouring salt beds (0.2 to 0.6‰), requiring a large, abrupt input of brine with negative δ37 Cl. Halite with high (0.6 – 0.8‰) δ37 Cl near the base of the East Slovakian and Transcarpathian evaporites requires a large input of chloride with positive δ37 Cl into the basins. Expulsion of basin brine with non-0‰δ37 Cl into the evaporite basins may account for the nonmarine chloride sources. 相似文献
13.
Genesis of Kanggur Gold Deposit in Eastern Tianshan Orogenic Belt, NW China: Fluid Inclusion and Oxygen and Hydrogen Isotope Constraints 总被引:3,自引:0,他引:3
Abstract. Primary fluid inclusions in quartz and carbonates from the Kanggur gold deposit are dominated by aqueous inclusions, with subsidiary CO2 -H2 O inclusions that have a constant range in CO2 content (10–20 vol %). Microthermometric results indicate that total homogenization temperatures have a wide but similar range for both aqueous inclusions (120 to 310C) and CO2 -H2 O inclusions (140 to 340C). Estimates of fluid salinity for CO2 -H2 O inclusions are quite restricted (5.9∼10.3 equiv. wt% NaCl), whereas aqueous inclusions show much wider salinity ranging from 2.2 to 15.6 equivalent wt %NaCl.
The 6D values of fluid inclusions in carbonates vary from -45 to -61 %, in well accord with the published δD values of fluid inclusions in quartz (-46 to -66 %). Most of the δ18 O and δD values of the ore-forming fluids can be achieved by exchanged meteoric water after isotopic equilibration with wall rock by fluid/rock interaction at a low water/rock ratio. However, the exchanged meteoric water alone cannot explain the full range of δ18 O and δD values, magmatic and/or meta-morphic water should also be involved. The wide salinity in aqueous inclusions may also result from mixing of meteoric water and magmatic and/or metamorphic water. 相似文献
The 6D values of fluid inclusions in carbonates vary from -45 to -61 %, in well accord with the published δD values of fluid inclusions in quartz (-46 to -66 %). Most of the δ
14.
One-dimensional advection-dispersion models predict that characteristic δ18 O vs. distance and δ18 O vs. δ13 C profiles should be produced during isothermal metamorphic fluid flow under equilibrium conditions. However, the patterns of isotopic resetting in rocks that have experienced fluid flow are often different from the predictions. Two-dimensional advection-dispersion simulations in systems with simple geometries suggest that such differences may be as a result of fluid channelling and need not indicate disequilibrium, high dispersivities, or polythermal flow. The patterns of isotopic resetting are a function of: (1) the permeability contrast between more permeable layers ('channels') and less permeable layers ('matrix'); (2) the width and spacing of the channels; (3) the width and spacing of discrete fractures; and (4) the orientation of the pressure gradient with respect to layering. In fractured systems, the efficiency of isotopic transport depends on the fracture aperture and the permeability of the surrounding rock. Resetting initially occurs along and immediately adjacent to the fractures, but with time isotopic resetting because of flow through the rock as a whole increases in importance. Application of the one-dimensional advection-dispersion equations to metamorphic fluid flow systems may yield incorrect estimates of fluid fluxes, intrinsic permeabilities, dispersivities, and permeability contrasts unless fluid flow occurred through zones of high permeability that were separated by relatively impermeable layers. 相似文献
15.
An Inter-Laboratory Assessment of the Thorium Isotopic Composition of Synthetic and Rock Reference Materials 总被引:2,自引:0,他引:2
Kenneth W.W. Sims James B. Gill Anthony Dosseto Dirk L. Hoffmann Craig C. Lundstrom Ross W. Williams Lary Ball Darren Tollstrup Simon Turner Julie Prytulak Justin J.G. Glessner J.J. Standish Tim Elliott 《Geostandards and Geoanalytical Research》2008,32(1):65-91
We present a concerted international effort to cross-calibrate five synthetic Th isotope reference materials (UCSC Th "A", OU Th "U", WUN, IRMM-35 and IRMM-36), and six rock reference materials (UCSC TML, Icelandic ATHO, USGS BCR-2, USGS W-2, USGS BHVO-2, LV18) using multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS). We then compare our new values with a compilation of literature mass spectrometric data for these reference materials and derive recommended "consensus"230 Th/232 Th values for each. We also present isotope dilution U and Th concentration data for four rock reference materials (UCSC TML, Icelandic ATHO, USGS BCR-2, USGS W-2). 相似文献
16.
Stable isotopic signature of a palaeoaquifer, Mississippian Alamogordo Member limestones, Sacramento Mountains, New Mexico, USA 总被引:1,自引:0,他引:1
Nine stratigraphic sections, each ≈5 m thick, were sampled from the Alamogordo Member limestones of the Lake Valley Formation, Sacramento Mountains, New Mexico, USA. Four stratigraphic sections consist entirely of lime mudstone and wackestone, whereas the other five sections have a prominent layer of crinoidal packstone about 1 m thick at their base. Stable isotopic analyses reveal that the lime muds in the sections with basal packstone layers show a downward decrease in δ18 O and constant δ13 C values, whereas those in the sections solely composed of lime mudstone and wackestone have, in general, relatively uniform δ18 O and δ13 C values. The diagenesis of the Alamogordo Member limestones was previously believed to have been governed by the downward percolation of meteoric water from a regional pre-Pennsylvanian exposure surface ≈100 m above this unit. However, the uniform δ13 C and downward decrease in δ18 O values in the lime muds in the sections with basal packstones indicate that the meteoric water ascended within the Alamogordo Member, rather than descended from the overlying exposure surface. This indicates that the basal packstones were probably a conduit for meteoric water. This is further supported indirectly by the relatively uniform δ18 O and δ13 C values of the lime mud in the sections without basal packstones. The implications are that the oxygen isotopic gradients may be used to identify palaeoaquifers, flow directions within these aquifers and that meteoric diagenesis below an exposure surface could be governed by flow through a palaeoaquifer. 相似文献
17.
Jens Wittenbrink Bernd Lehmann Michael Wiedenbeck Alex Wallianos reas Dietrich Carlos Palacios 《地学学报》2009,21(2):111-118
Quartz-hosted melt inclusions from latite dykes of the Eocene El Salvador copper porphyry system in northern Chile display wide ranges in both boron concentration (15–155 p.p.m. B) and isotope composition (δ11 B −7 to +12‰; n = 10), likely reflecting slab-derived fluid input from seawater-altered oceanic crust. In contrast, the major Miocene tin-silver and tin porphyry systems in the Bolivian back-arc region (Cerro Rico de Potosi, Chorolque, Llallagua) have distinctly different melt inclusion compositions with δ11 B of −11.4 ± 2.7‰ ( n = 10), and magmatic boron enrichment up to several hundred p.p.m. B. The `seawater' signature in the El Salvador melt inclusions explains the oxidized mineral assemblage of the copper porphyry system, as opposed to the more reduced nature of the Bolivian tin porphyry systems, which reflect intracrustal melting of pelitic rocks. 相似文献
18.
Abstract. Carboniferous-Permian limestones of the Akiyoshi Plateau, in the Inner Zone of southwestern Japan, are composed of essentially pure calcium carbonate containing only small amounts of other elements, and they are accompanied by marble and copper skarn deposits near the contact with late Cretaceous granitoids. The δ18 O values of the Akiyoshi limestones range widely from 7.6 to 28.3% and are mostly lower than those of other areas of the same age (23–29%), whereas the differences among the δ13 C values are small. The δ18 O values are negatively correlated with Mn and Fe contents. Samples with high δ18 O (>25%) and δ13 C (>2%) values do not contain Fe, Zn, or Pb, but those with low δ18 O values tend to be rich in these elements, indicating that these elements were introduced by interaction with H2 O dominant fluids, possibly of magmatic origin. Potential scores for evaluating the degree of interaction with hydro thermal fluids were calculated for δ18 O, δ13 C, Fe, Mn, Zn, Pb, and Sr. Higher scores implying much hydrothermal interaction were evident in the Mt. Hananoyama area, where there are many skarn deposits, and along faults oriented mainly NNW-SSE. Therefore, these are promising areas for exploring for blind deposits. It is likely that the hydrothermal fluid traveled through the limestones along fractures at the time of the granitic intrusions. However, the potential scores here are much smaller than those in the Pb-Zn mineralized area of the Kamioka mine, so more detailed petrological and mineralogical investigations are necessary. 相似文献
19.
VEERLE VANDEGINSTE RUDY SWENNEN SARAH A. GLEESON† ROB M. ELLAM‡ KIRK OSADETZ§ FRANÇOIS ROURE¶ 《Sedimentology》2009,56(2):439-460
The Fairholme carbonate complex is part of the extensively dolomitized Upper Devonian carbonate reefs in west-central Alberta. The studied formations contain moulds (up to 10 cm in diameter), which are filled partially with (saddle) dolomite, quartz and calcite cements. These cements precipitated from a mixture of brines that acquired high salinity by dissolution of halite and brines derived from evaporated sea water. The fluids were warm (homogenization temperature of primary fluid inclusions of 76 to 200 °C) and saline (20 to 25 wt% NaCl equivalent) and testify to thermochemical sulphate reduction processes. The latter is deduced from S in solid inclusions, CO2 and H2 S in volatile-rich aqueous inclusions and depleted δ13 C values down to −26‰ Vienna Pee Dee Belemnite. High 87 Sr/86 Sr values (0·7094 to 0·7110) of the cements also indicate interaction of the fluids with siliciclastic sequences. The thermochemical sulphate reduction-related cements probably formed during early Laramide burial. Another (younger) calcite phase, characterized by depleted δ18 O values (−23·9‰ to −13·9‰ Vienna Pee Dee Belemnite), low Na (27 to 37 p.p.m.) and Sr (39 to 150 p.p.m.) concentrations and non-saline (∼0 wt% NaCl equivalent) fluid inclusions, is attributed to post-Laramide meteoric water. 相似文献
20.
Seasonal and interannual variability of Siberian river discharge in the Laptev Sea inferred from stable isotopes in modern bivalves 总被引:2,自引:0,他引:2
THOMAS MUELLER-LUPP HELMUT ERLENKEUSER HENNING A. BAUCH 《Boreas: An International Journal of Quaternary Research》2003,32(2):292-303
Stable oxygen and carbon isotope profiles from modern bivalve shells were investigated in order to reconstruct short-term hydrographical changes in the river-shelf system of the Laptev Sea. Oxygen isotopic profiles obtained from the aragonitic species Astarte borealis exhibit amplitude cycles interpreted as annual hydrographical cycles. These records reflect the strong contrast between summer and winter bottom water conditions in the Laptev Sea. The seasonal variations in δ18 O are mainly controlled by the riverine freshwater discharge during summer with 0.5‰ per salinity unit. Corrected for a defined species-dependent fractionation offset of -0.37‰, time-dependent salinity records were reconstructed from these δ18 O profiles. They indicate a good correspondence to seasonal hydrographic changes and synoptical data. Persistent trends with shell growth towards more negative δ13 C values are observed in all specimens and appear to be related to metabolic changes of the bivalves during ontogeny. In contrast, short-term fluctuations are likely linked to seasonal variabilities of the river water outflow patterns and enhanced phytoplankton productivity during summer. This is corroborated by a clear watermass-related distinction of the various δ13 C records made on the basis of water depth and distance from the riverine source. 相似文献