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Oxygen Isotope Composition (oxygen + isotope_composition)
Selected AbstractsInvasion of a karst aquifer by hydrothermal fluids: evidence from stable isotopic compositions of cave mineralizationGEOFLUIDS (ELECTRONIC), Issue 2 2001S. H. Bottrell Abstract Mineral deposits in the Cupp-Coutunn/Promeszutochnaya cave system (Turkmenia, central Asia) record a phase of hydrothermal activity within a pre-existing karstic groundwater conduit system. Hydrothermal fluids entered the caves through fault zones and deposited sulphate, sulphide and carbonate minerals under phreatic conditions. Locally, intense alteration of limestone wall rocks also occurred at this stage. Elsewhere in the region, similar faults contain economic quantities of galena and elemental sulphur mineralization. Comparisons between the Pb and S isotope compositions of minerals found in cave and ore deposits confirm the link between economic mineralization and hydrothermal activity at Cupp-Coutunn. The predominance of sulphate mineralization in Cupp-Coutunn implies that the fluids were more oxidized in the higher permeability zone associated with the karst aquifer. A slight increase in the ,34S of sulphate minerals and a corresponding ,34S decrease in sulphides suggest that partial isotopic equilibration occurred during oxidation. Carbonate minerals indicate that the hydrothermal fluid was enriched in 18O (,18OSMOW , + 10,) relative to meteoric groundwater and seawater. Estimated values for ,13CDIC (,13CPDB , , 13,) are consistent with compositions expected for dissolved inorganic carbon (DIC) derived from the products of thermal decomposition of organic matter and dissolution of marine carbonate. Values derived for ,13CDIC and ,18Owater indicate that the hydrothermal fluid was of basinal brine origin, generated by extensive water,rock interaction. Following the hydrothermal phase, speleothemic minerals were precipitated under vadose conditions. Speleothemic sulphates show a bimodal sulphur isotope distribution. One group has compositions similar to the hydrothermal sulphates, whilst the second group is characterized by higher ,34S values. This latter group may either record the effects of microbial sulphate reduction, or reflect the introduction of sulphate-rich groundwater generated by the dissolution of overlying evaporites. Oxygen isotope compositions show that calcite speleothems were precipitated from nonthermal groundwater of meteoric origin. Carbonate speleothems are relatively enriched in 13C compared to most cave deposits, but can be explained by normal speleothem-forming processes under thin, arid-zone soils dominated by C4 vegetation. However, the presence of sulphate speleothems, with isotopic compositions indicative of the oxidation of hydrothermal sulphide, implies that CO2 derived by reaction of limestone with sulphuric acid (,condensation corrosion') contributed to the formation of 13C-enriched speleothem deposits. [source] Speleothem preservation and diagenesis in South African hominin sites implications for paleoenvironments and geochronologyGEOARCHAEOLOGY: AN INTERNATIONAL JOURNAL, Issue 5 2009Philip J. Hopley Plio-Pleistocene speleothems from australopithecine-bearing caves of South Africa have the potential to yield paleoenvironmental and geochronological information using isotope geochemistry. Prior to such studies it is important to assess the preservation of geochemical signals within the calcitic and aragonitic speleothems, given the tendency of aragonitic speleothems to recrystallize to calcite. This study documents the geochemical suitability of speleothems from the principal hominin-bearing deposits of South Africa. We use petrography, together with stable isotope and trace element analysis, to identify the occurrence of primary aragonite, primary calcite, and secondary calcite. This study highlights the presence of diagenetic alteration at many of the sites, often observed as interbedded primary and secondary fabrics. Trace element and stable isotopic values distinguish primary calcite from secondary calcite and offer insights into geochemical aspects of the past cave environment. ,13C values of the primary and secondary calcites range from +6 to ,9, and ,18O values range from ,4 to ,6,. The data are thus typical of meteoric calcites with highly variable ,13C and relatively invariant ,18O. High carbon isotope values in these deposits are associated with the effects of recrystallization and rapid outgassing of CO2 during precipitation. Mg/Ca and Sr/Ca ratios differ between primary and secondary calcite speleothems, aiding their identification. Carbon and oxygen isotope values in primary calcite reflect the proportion of C3 and C4 vegetation in the local environment and the oxygen isotope composition of rainfall. Primary calcite speleothems preserve the pristine geochemical signals vital for ongoing paleoenvironmental and geochronological research. © 2009 Wiley Periodicals, Inc. [source] Strong seasonal disequilibrium measured between the oxygen isotope signals of leaf and soil CO2 exchangeGLOBAL CHANGE BIOLOGY, Issue 11 2010LISA WINGATE Abstract The oxygen isotope composition (,18O) of atmospheric CO2 is among a very limited number of tools available to constrain estimates of the biospheric gross CO2 fluxes, photosynthesis and respiration at large scales. However, the accuracy of the partitioning strongly depends on the extent of isotopic disequilibrium between the signals carried by these two gross fluxes. Chamber-based field measurements of total CO2 and CO18O fluxes from foliage and soil can help evaluate and refine our models of isotopic fractionation by plants and soils and validate the extent and pattern of isotopic disequilibrium within terrestrial ecosystems. Owing to sampling limitations in the past, such measurements have been very rare and covered only a few days. In this study, we coupled automated branch and soil chambers with tuneable diode laser absorption spectroscopy techniques to continuously capture the ,18O signals of foliage and soil CO2 exchange in a Pinus pinaster Aďt forest in France. Over the growing season, we observed a seasonally persistent isotopic disequilibrium between the ,18O signatures of net CO2 fluxes from leaves and soils, except during rain events when the isotopic imbalance became temporarily weaker. Variations in the ,18O of CO2 exchanged between leaves, soil and the atmosphere were well explained by theory describing changes in the oxygen isotope composition of ecosystem water pools in response to changes in leaf transpiration and soil evaporation. [source] Estimating the timing of growth rings in Atlantic cod otoliths using stable oxygen isotopesJOURNAL OF FISH BIOLOGY, Issue 3 2006H. Hřie A technique involving micro-scale sampling of otolith carbonate and analyses of stable oxygen isotope composition was used to relate the zone appearance of the otolith to the seasonal temperature cycle. Otolith opacity could then be related to the timing of zone formation. Otoliths from two groups of Atlantic cod Gadus morhua held under known temperature conditions over a period of 4 and 6 years were examined. The otolith translucency followed the same pattern as the estimated temperature (from otolith ,18O values) in the yearly increments three and four, meaning that the translucent zones were deposited at the seasonal highest temperature in late summer and early autumn. The relative light intensities of otolith yearly increments five and six of older fish (deposited in the same years), however, were not significantly correlated to the estimated temperatures since increased otolith translucency also occurred at low temperatures. This might have been caused by stress in connection with gonad development or starvation during the spawning period. The results showed that this method of coupling otolith opacity and stable oxygen isotope composition can be used to estimate the timing of zone formations in otoliths. [source] Combined oxygen and silicon isotope analysis of biogenic silica,JOURNAL OF QUATERNARY SCIENCE, Issue 4 2008Melanie J. Leng Abstract There is increasing interest in the use of biogenic silica O and Si isotope ratios to understand climate and environmental processes. Virtually all of the fairly substantial body of literature deals with either oxygen or silicon. This is partly because measurement of oxygen isotope composition is done using either vacuum dehydration, isotope exchange or stepped fluorination techniques, while increasingly researchers are turning to multicollector inductively coupled plasma mass spectrometry (MC-ICP-MS) for Si isotope analysis, even though Si isotope analysis can be done using fluorination methods used for the oxygen isotope measurements. Here we describe a procedure for simultaneous determination of isotopic abundances of oxygen and silicon from the same aliquot of biogenic silica. Pure silica is dissociated into O and Si compounds using a fluorination technique, in which reaction with bromine pentafluoride (BrF5) produces oxygen (O2, subsequently converted to CO2), silicon tetrafluoride (SiF4) and other fluorine by-products (e.g. BrF3). These compounds are cryogenically separated using cold traps. Yields for oxygen and silicon recovery are 70,80% for biogenic silica depending on the nature of the hydrous layer and 97,99% for pure quartz. Reproducibility of the oxygen isotopic composition is ca. 0.3, and silicon between 0.06,0.12,. © Natural Environment Research Council (NERC) copyright 2008. Reproduced with the permission of NERC. Published by John Wiley & Sons, Ltd. [source] Holocene climate change in the eastern Mediterranean region: a comparison of stable isotope and pollen data from Lake Gölhisar, southwest Turkey,JOURNAL OF QUATERNARY SCIENCE, Issue 4 2007Warren J. Eastwood Abstract Stable isotope and pollen data from Gölhisar Gölü, a small intramontane lake located in southwest Turkey, provide complementary records of Holocene climate change. Modern oxygen and hydrogen isotope water data are used as a means of comparing present-day isotope composition of the lake water to the past oxygen isotope composition of the lake water as calculated from 18O/16O ratios in calcite precipitated in the summer months. Despite the lake system being chemically dilute, the modern isotope data clearly establish that the lake water is evaporated in relation to its spring input, suggesting that the palaeo data can be interpreted primarily in terms of changing precipitation/evaporation ratios. ,18O and ,13C values from authigenic calcite through the Holocene show predominantly negative values indicating climatic conditions wetter than today. Particularly notable are low (depleted) isotope values during the earliest Holocene (ca. 10,600,8800 cal. yr. BP), a period for which pollen data imply drier conditions than at present. This divergence between pollen-inferred and stable isotope palaeoclimate data is found in other east Mediterranean lake sediment records, and suggests that vegetation may have taken several millennia to reach climatic equilibrium at the start of the Holocene. Isotopic fluctuations during the early-to-mid Holocene (8800,5100 cal. yr. BP) suggest oscillations between aridity and humidity. Higher ,18O and ,13C values for the second half of the Holocene indicate generally drier conditions than during the period before ca.5100 cal. yr BP although there is some evidence for increased humidity coinciding with pollen evidence for increasing human impact and intensification of agriculture, notably during the so-called Bey,ehir Occupation Phase (Classical and early Byzantine periods). The modern trend towards aridity started about 1300 yr ago. Copyright © 2006 John Wiley & Sons, Ltd. [source] Relationships of grain ,13C and ,18O with wheat phenology and yield under water-limited conditionsANNALS OF APPLIED BIOLOGY, Issue 2 2007J.P. Ferrio Abstract Stable carbon isotope composition (,13C) of dry matter has been widely investigated as a selection tool in cereal breeding programmes. However, reports on the possibilities of using stable oxygen isotope composition (,18O) as a yield predictor are very scarce and only in the absence of water stress. Indeed, it remains to be tested whether changes in phenology and stomatal conductance in response to water stress overrule the use of either ,13C or ,18O when water is limited. To answer this question, a set of 24 genotypes of bread wheat (Triticum aestivum) were assayed in two trials with different levels of deficit irrigation and a third trial under rainfed conditions in a Mediterranean climate (northwest Syria). Grain yield (GY) and phenology (duration from planting to anthesis and from anthesis to maturity) were recorded, and the ,13C and ,18O of grains were analysed to assess their suitability as GY predictors. Both ,13C and ,18O showed higher broad-sense heritabilities (H2) than GY. Genotype means of GY across trials were negatively correlated with ,13C, as previously reported, but not with ,18O. Both isotopes were correlated with grain filling duration, whereas ,18O was also strongly affected by crop duration from planting to anthesis. We concluded that ,18O of grains is not a proper physiological trait to breed for suboptimal water conditions, as its variability is almost entirely determined by crop phenology. In contrast, ,13C of grains, despite being also affected by phenology, still provides complementary information associated with GY. [source] Carbon and Oxygen Isotopic Composition of Surface-Sediment Carbonate in Bosten Lake (Xinjiang, China) and its Controlling FactorsACTA GEOLOGICA SINICA (ENGLISH EDITION), Issue 2 2009Chengjun ZHANG Abstract: Bosten Lake is a mid-latitude lake with water mainly supplied by melting ice and snow in the Tianshan Mountains. The depositional environment of the lake is spatially not uniform due to the proximity of the major inlet and the single outlet in the western part of the lake. The analytical results show that the carbon and oxygen isotopic composition of recent lake sediments is related to this specific lacustrine depositional environment and to the resulting carbonate mineralogy. In the southwestern lake region between the Kaidu River inlet and the Kongqi River outlet, carbon isotope composition (,13C) values of the carbonate sediment (,1, to ,2,) have no relation to the oxygen isotope composition of the carbonate (,18O) values (,7, to ,8,), with both isotopes showing a low variability. The carbonate content is low (<20%). Carbonate minerals analyzed by X-ray diffraction are mainly composed of calcite, while aragonite was not recorded. The salinity of the lake water is low in the estuary region as a result of the Kaidu River inflow. In comparison, the carbon and oxygen isotope values are higher in the middle and eastern parts of the lake, with ,13C values between approximately +0.5, and +3,, and ,18O values between ,1, and ,5,. There is a moderate correlation between the stable oxygen and carbon isotopes, with a coefficient of correlation r of approximately 0.63. This implies that the lake water has a relatively short residence time. Carbonate minerals constitute calcite and aragonite in the middle and eastern region of the lake. Aragonite and Mg,calcite are formed at higher lake water salinity and temperatures, and larger evaporation effects. More saline lake water in the middle and eastern region of the lake and the enhanced isotopic equilibrium between water and atmospheric CO2 cause the correlating carbon and oxygen isotope values determined for aragonite and Mg,calcite. Evaporation and biological processes are the main reasons for the salinity and carbonate mineralogy influence of the surface-sediment carbonate in Bosten Lake. The lake water residence time and the CO2 exchange between the atmosphere and the water body control the carbon and oxygen isotope composition of the carbonate sediment. In addition, organic matter pollution and decomposition result in the abnormally low carbon isotope values of the lake surface-sediment carbonate. [source] Syntectonic infiltration by meteoric waters along the Sevier thrust front, southwest MontanaGEOFLUIDS (ELECTRONIC), Issue 4 2006A. C. RYGEL Abstract Structural, petrographic, and isotopic data for calcite veins and carbonate host-rocks from the Sevier thrust front of SW Montana record syntectonic infiltration by H2O-rich fluids with meteoric oxygen isotope compositions. Multiple generations of calcite veins record protracted fluid flow associated with regional Cretaceous contraction and subsequent Eocene extension. Vein mineralization occurred during single and multiple mineralization events, at times under elevated fluid pressures. Low salinity (Tm = ,0.6°C to +3.6°C, as NaCl equivalent salinities) and low temperature (estimated 50,80°C for Cretaceous veins, 60,80°C for Eocene veins) fluids interacted with wall-rock carbonates at shallow depths (3,4 km in the Cretaceous, 2,3 km in the Eocene) during deformation. Shear and extensional veins of all ages show significant intra- and inter-vein variation in ,18O and ,13C. Carbonate host-rocks have a mean ,18OV-SMOW value of +22.2 ± 3, (1,), and both the Cretaceous veins and Eocene veins have ,18O ranging from values similar to those of the host-rocks to as low as +5 to +6,. The variation in vein ,13CV-PDB of ,1 to approximately +6, is attributed to original stratigraphic variation and C isotope exchange with hydrocarbons. Using the estimated temperature ranges for vein formation, fluid (as H2O) ,18O calculated from Cretaceous vein compositions for the Tendoy and Four Eyes Canyon thrust sheets are ,18.5 to ,12.5,. For the Eocene veins within the Four Eyes Canyon thrust sheet, calculated H2O ,18O values are ,16.3 to ,13.5,. Fluid,rock exchange was localized along fractures and was likely coincident with hydrocarbon migration. Paleotemperature determinations and stable isotope data for veins are consistent with the infiltration of the foreland thrust sheets by meteoric waters, throughout both Sevier orogenesis and subsequent orogenic collapse. The cessation of the Sevier orogeny was coincident with an evolving paleogeographic landscape associated with the retreat of the Western Interior Seaway and the emergence of the thrust front and foreland basin. Meteoric waters penetrated the foreland carbonate thrust sheets of the Sevier orogeny utilizing an evolving mesoscopic fracture network, which was kinematically related to regional thrust structures. The uncertainty in the temperature estimates for the Cretaceous and Eocene vein formation prevents a more detailed assessment of the temporal evolution in meteoric water ,18O related to changing paleogeography. Meteoric water-influenced ,18O values calculated here for Cretaceous to Eocene vein-forming fluids are similar to those previously proposed for surface waters in the Eocene, and those observed for modern-day precipitation, in this part of the Idaho-Montana thrust belt. [source] | |||||||||||||