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1.
We tested the effectiveness of stable isotopes as recorders of physiological changes that occur during coral bleaching and recovery. Montipora capitata and Porites compressa fragments were bleached in outdoor tanks with seawater temperature raised to 30 °C (treatment corals) for one month. Additional fragments were maintained at 27 °C in separate tanks (control corals). After one month, (0 months recovery), buoyant weight was measured and a subset of fragments was frozen. Remaining fragments were returned to the reef for recovery. After 1.5, 4, and 8 months, fragments were collected, measured for buoyant weight, and frozen. Fragments were analyzed for stable carbon and oxygen isotopic compositions of the skeleton (δ13Cs; δ18Os) and nitrogen and carbon isotopic compositions of the host tissue (δ15Nh; δ13Ch) and zooxanthellae (δ15Nz; δ13Cz). δ13Cs decreased immediately after bleaching in M. capitata, but not in P. compressa. δ18Os of both species failed to record the warming event. During the remaining months of recovery, δ13Cs and δ18Os were more enriched in treatment than control corals due to decreases in calcification and metabolic fractionation during that time. Increased δ15Nh of treatment P. compressa may be due to expelled zooxanthellae during bleaching and recovery. Increased δ15Nz at 1.5 months in treatment fragments of both species reflects the increased incorporation of dissolved inorganic nitrogen to facilitate mitotic cell division and/or chl a/cell recovery. Changes in δ13Ch and δ13Cz at 1.5 months in treatment M. capitata indicated a large increase in heterotrophically acquired carbon relative to photosynthetically fixed carbon. We experimentally show that isotopes in coral skeleton, host tissue and zooxanthellae can be used to verify physiological changes during bleaching and recovery, but their use as a proxy for past bleaching events in the skeletal record is limited.  相似文献   

2.
Offsets from isotopic equilibrium in biogenic carbonates have complicated paleoclimate reconstructions for decades. A new archive of climate, deep-sea corals, is used to evaluate the calcification processes, independent of photosynthesis, that contribute to these offsets. Carbon and oxygen stable isotope data from six modern deep-sea corals show strong linear trends between δ13C and δ18O. Slopes of these trends between samples are similar and range between 1.9 to 2.6 for Δδ13C/Δδ18O. Linear trends intersect isotopic equilibrium for δ18O and are slightly depleted for δ13C. Variations in the isotopic ratios are strongly correlated with the density banding structure. Isotopically depleted aragonite is associated with light, quickly precipitating bands, whereas isotopically enriched points correspond to slowly accumulating, less dense aragonite. The densest white band at the trabecular center is furthest from isotopic equilibrium for both carbon and oxygen. Data from this region fall off the linear trend between δ18O and δ13C. This deviation, where δ13C remains constant while the δ18O continues to decrease, does not support “vital effect” mechanisms that call upon kinetic fractionation to explain offsets from isotopic equilibrium. We propose a new mechanism for vital effects in these deep-sea corals that is based on a thermodynamic response to a biologically induced pH gradient in the calcifying region.  相似文献   

3.
Cellulose and silica phytoliths were extracted from the leaves and stems of Calamovilfa longifolia, a C4 grass, grown under varying climatic conditions across the North American prairies. The oxygen-isotope compositions of both cellulose and silica record a complex signal of the isotopic composition of the soil water that feeds the plants and the relative humidity conditions that influence transpiration rates, stomatal conductance, and ultimately the 18O-enrichment of leaf water. As the initial stages of cellulose formation occur in the leaves, cellulose in both the leaves and stems forms primarily from leaf water and does not differ greatly in its oxygen-isotope composition between these locations. In contrast, the δ18O values of leaf phytoliths are significantly enriched in 18O relative to stem phytoliths, reflecting the varying isotopic composition of the water in these tissues. The oxygen-isotope compositions of leaf cellulose may be used as a proxy for the isotopic composition of water involved in leaf phytolith formation, while the δ18O values of stem phytoliths can be used to determine the δ18O values of stem water involved in partial exchange reactions during the transport of carbohydrates through the plant. A comparison of the isotopic compositions of phytoliths with cellulose allows for the deduction of soil and leaf water δ18O values as well as temperature and relative humidity conditions during plant growth. This approach has application in paleoclimate studies that traditionally have required estimations of one or more of these variables because direct measurements were unavailable.  相似文献   

4.
5.
We discuss water oxygen isotopes (δ18Ow) and carbon isotopes of dissolved inorganic carbon (δ13CDIC) of brine‐enriched shelf water (BSW) from Storfjorden (southern Svalbard) in comparison to Recent benthic foraminiferal δ18Oc and δ13Cc calcified in the same water. We determined relatively high δ18Ow values of 0.15±0.03‰ VSMOW in BSW below sill depth at temperatures below ?1.8 °C, and high δ18Oc values of 3.90±0.18‰ VPDB. Such high BSW δ18Ow cannot significantly deplete 18Ow contents of Arctic Ocean deep water; furthermore, such high δ18Oc cannot be distinguished from δ18Oc values of 3.82±0.12‰, calcified in warmer Arctic and Nordic seas intermediate and deeper waters. Today, in Storfjorden low benthic δ13Cc and high δ18Oc reflect the low δ13CDIC and relatively high δ18Ow of BSW. High benthic δ18Oc is in contrast to expected low δ18Oc as brine rejection is widely thought to predominantly take place in surface water diluted by meteoric water with very low δ18Ow. Low epibenthic δ13Cc values of 0.50±0.12‰ partly reflect low δ13CDIC caused by enhanced uptake of atmospheric low δ13CCO2 decreased by anthropogenic activities. An adjustment for preindustrial higher values would increase δ13Cc by about 0.6‰. Therefore, in Storfjorden brine formed before the industrial era would be characterized by both high δ13Cc as well as high δ18Oc values of benthic foraminiferal calcite. Our data may cast doubt on scenarios that explain negative excursions in benthic foraminiferal stable isotope records from the Atlantic Ocean during cold stadials in the last glacial period by enhanced brine formation in Nordic seas analogously to modern processes in Storfjorden.  相似文献   

6.
The present multi-isotopic study (δ18O–δDwater, δ34S–δ18Odissolved-sulphate, δ13Cdissolved-inorganic-carbon, δ13C–δ18Oshells-modern-gastropods, δ13Cplants, and δ13Csedimentary-organic-matter) is aimed at assessing the hydrogeochemical changes and biogeochemical dynamics in a Mediterranean shallow lake fed by a Quaternary–Tertiary aquifer, the “Laguna del Cristo” (NW Iberian Peninsula), a system sensitive to climate fluctuations, between 2010 and 2011. Lake water is of the bicarbonate type, and there are no major pollutants. δ18O-δDwater values plot on a local evaporation line (δD=5.29δ18O–12.29) indicating that evaporative enrichment had a significant impact on lake water isotopic features. Periods of high water levels are characterized by lower δ34S–δ18Odissolved-sulphate and δ13Cdissolved-inorganic-carbon values and suggest sulphate derived from weathering of sulphides in the catchment area, delivered to the lake by surface run-off or via groundwater, and in situ decay of organic matter. During lower water levels, sulphate reduction and enhanced primary productivity lead to higher δ34Sdissolved-sulphate and δ13Cdissolved-inorganic-carbon values. Evaporation induced enrichment in 18Osulphate, 13Cdissolved-inorganic-carbon and 13C–18Oshells-Galba-Gyraulus. δ13Cplant confirms the C3 photosynthetic pathway. Enrichment in 13C submerged aquatic plants indicates that HCO3? is the main carbon source, except for 13C-depleted Potamogeton. The TOC, δ13Corg values, and TC/TN ratios in sediments all confirm the autochthonous character of organic matter contribution. This study provides a baseline for isotopic research into shallow, flow-through lakes fed by siliciclastic aquifers, and stresses the importance of evaporation and refilling (direct precipitation and groundwater discharge) in controlling the solute chemistry and stable isotopic composition in temperate regions with contrasting seasonal climates. The results also provide a snapshot of modern lake isotope variability that can be applied to paleoenvironmental reconstructions.  相似文献   

7.
The oxygen isotope compositions of diagenetic carbonate minerals from the Lower Jurassic Inmar Formation, southern Israel, have been used to identify porewater types during diagenesis. Changes in porewater composition can be related to major geological events within southern Israel. In particular, saline brines played an important role in late (Pliocene-Pleistocene) dolomitization of these rocks. Diagenetic carbonates included early siderite (δ18OSMOW=+24.4 to +26.5‰δ13CPDB=?1.1 to +0.8‰), late dolomite, ferroan dolomite and ankerite (δ18OSMOW=+18.4 to +25.8‰; δ13CPDB=?2.1 to +0.2‰), and calcite (δ18OSMOW=+21.3 to +32.6‰; δ13CPDB=?4.2 to + 3.2‰). The petrographic and isotopic results suggest that siderite formed early in the diagenetic history at shallow depths. The dolomitic phases formed at greater depths late in diagenesis. Crystallization of secondary calcite spans early to late diagenesis, consistent with its large range in isotopic values. A strong negative correlation exists between burial depth (temperature) and the oxygen isotopic compositions of the dolomitic cements. In addition, the δ18O values of the dolomitic phases in the northern Negev and Judea Mountains are in isotopic equilibrium with present formation waters. This behaviour suggests that formation of secondary dolomite post-dates the tectonic activity responsible for the present relief of southern Israel (Upper Miocene to Pliocene) and that the dolomite crystallized from present formation waters. Such is not the case in the Central Negev. In that locality, present formation waters have much lower salinities and δ18O values, indicating invasion of freshwater, and are out of isotopic equilibrium with secondary dolomite. Recharge of the Inmar Formation by meteoric water in the Central Negev occurred in the Pleistocene, and halted formation of dolomite.  相似文献   

8.
The isotopic composition of dissolved inorganic carbon (DIC) in estuarine environments has been studied for its significant role in determining the isotopic composition of inorganic/organic matter and its applications to the study of various natural processes. In this paper, based on the stable isotope geochemical characteristics of dis- solved inorganic carbon in the Jiulong River Estuary, the following conclusions are drawn: (1) δ13CDIC values are mainly controlled by the mixing ratio of fresh water and sea water; (2)δ13Cphytoplankton values are linearly related to the δ13CDIC values; (3) δ13CpoM values for the Jiulong River Estuary are affected by anthropogenic pollution signifi- cantly; and (4) the comprehensive analysis of δ13Cphytoplankton, δ13CpoM and δ13CDIc shows that along with increasing salinity, the proportion of POM derived from the degradation of phytoplanktons gradually increases.  相似文献   

9.
The build up of the isotopic signal in corals was followed by sampling the newly formed skeleton at a monthly resolution for a period of two years in order to establish the interrelations between the calcification processes and the skeletal isotopic composition. We deployed two underwater sampling schemes, which provide a monitor of the changes in water temperature and δ18O and in the corresponding newly accreted skeleton of undisturbed Porites lutea colonies under natural conditions and four transplanted colonies, which maintained the genetic identity throughout the experiment. The results indicate that δ18O of the newly accreted skeleton does not correlate with ambient temperature although the seasonal temperature variability at the site (winter to summer) is in the order of 6 °C and δ18O of seawater is constant throughout the year. In contrast to the newly formed surface skeleton, the isotopic compositions of the deep and older parts of the skeleton show the predicted annual isotopic pattern with highly significant correlation between δ18Os and SST. The transformation between temperature-independent to temperature-dependent isotopic signal occurs several months after the skeleton was formed at the surface. The position of the skeleton in relation to the open sea may generate the difference between δ18Os of the surface skeleton and that of the skeleton previously accreted further down the tissue layer. Our data support the general model of a multi-step skeletogenesis process, where the temperature independent skeleton is entails the first step, the production of skeletal scaffold, and the environmental temperature signature is captured by the next two other steps: the thickening and the periodic abrupt uplift occurring at the depth of the tissue layer. However, re-examination and development of the current isotopic models for coral calcification are required in order to explain the observed different temperature dependency during the growth’s sequence.  相似文献   

10.
《Applied Geochemistry》2002,17(9):1241-1257
This study aimed to develop a methodology for assessing the hydrochemical evolution of a groundwater system, using fracture-filling and fracture-lining calcite. Fracture calcite in deep (to ca. 1000 m) granitic rocks of the Tono area, central Japan, was investigated by optical and electron microscopy, and chemical and isotopic analysis. Coupled with geological evidence, these new data imply 3 main origins for the waters that precipitated calcite: (1) relatively high-temperature hydrothermal solutions, precipitating calcite distinguished by δ18OSMOW from −3 to ca. 10‰, and with δ13CPDB from ca. −18 to −7‰; (2) seawater, probably partly of Miocene age, which precipitated calcite distinguished by δ13CPDB of ca. 0‰ and δ18OSMOW > ca. 20‰; (3) fresh water, with a variable δ13CPDB composition, but which precipitated calcite distinguished by δ13CPDB that was significantly < 0‰ and as low as ca. −29‰ and δ18OSMOW > ca. 17‰. Data for 14C suggest that at least some of the fresh-water calcite formed within the last 50 ka. The present day hydrogeological regime in the Tono area is also dominated by fresh groundwater. However, the marine calcite of probable Miocene age found at depth has shown no evidence for dissolution and many different calcite crystal forms have been preserved. Studies of other groundwater systems have correlated similar crystallographic variations with variations in the salinity of coexisting groundwaters. When this correlation is applied to the Tono observations, the calcite crystal forms imply a similar range of groundwater salinity to that inferred from the isotopic data. Thus, the present study suggests that even in presently low-salinity groundwater systems, calcite morphological variations may record the changing salinity of coexisting groundwaters. It is suggested that calcite morphological data, coupled with isotopic data, could provide a powerful palaeohydrogeological tool in such circumstances.  相似文献   

11.
Information regarding climatic conditions during plant growth is preserved by the oxygen-isotope composition of biogenic silica (phytoliths) deposited in grasses. The O-isotope compositions of phytoliths and the plant water from which they precipitate are dependent on soil-water δ18O values, relative humidity, evapotranspiration rates, and temperature. Plant water and phytoliths from two grass species, Ammophila breviligulata (C3) and Calamovilfa longifolia (C4) at Pinery Provincial Park in southwestern Ontario, Canada, were examined to determine the variability in their δ18O values. Stem water was unfractionated from soil-water in oxygen isotopic composition and the δ18O values of stem silica provide a good proxy for the soil water available to roots during the growing season. Greater spatial and temporal variation in the δ18O values of water in the top 5 cm of the soil, and their enhanced sensitivity to evaporative 18O enrichment, are reflected in the generally higher δ18O values of water in the shallow roots and rhizomes of these grasses. Water within the sheath and lower and upper leaf tissues experiences continual evaporation, becoming progressively enriched in 18O as it moves towards the tip of the leaf. However, the water from which leaf silica precipitates has not acquired the extreme 18O enrichment predicted using steady-state models, or measured for midday or average daily leaf water. Possible explanations for this behaviour include preferential deposition of silica at night; the existence of a secluded water fraction within the leaf, which experiences smaller diurnal variations in isotopic composition than leaf water at sites of evaporation; kinetic isotope effects during rapid precipitation of leaf silica; and incomplete exchange between the oxygen in the silicic acid and the leaf water.  相似文献   

12.
Abstract Large calcite veins and pods in the Proterozoic Corella Formation of the Mount Isa Inlier provide evidence for kilometre-scale fluid transport during amphibolite facies metamorphism. These 10- to 100-m-scale podiform veins and their surrounding alteration zones have similar oxygen and carbon isotopic ratios throughout the 200 × 10-km Mary Kathleen Fold Belt, despite the isotopic heterogeneity of the surrounding wallrocks. The fluids that formed the pods and veins were not in isotopic equilibrium with the immediately adjacent rocks. The pods have δ13Ccalcite values of –2 to –7% and δ18Ocalcite values of 10.5 to 12.5%. Away from the pods, metadolerite wallrocks have δ18Owhole-rock values of 3.5 to 7%. and unaltered banded calc-silicate and marble wallrocks have δ13Ccalcite of –1.6 to –0.6%, and δ18Ocalcite of 18 to 21%. In the alteration zones adjacent to the pods, the δ18O values of both metadolerite and calc-silicate rocks approach those of the pods. Large calcite pods hosted entirely in calc-silicates show little difference in isotopic composition from pods hosted entirely in metadolerite. Thus, 100- to 500-m-scale isotopic exchange with the surrounding metadolerites and calc-silicates does not explain the observation that the δ18O values of the pods are intermediate between these two rock types. Pods hosted in felsic metavolcanics and metasiltstones are also isotopically indistinguishable from those hosted in the dominant metadolerites and calc-silicates. These data suggest the veins are the product of infiltration of isotopically homogeneous fluids that were not derived from within the Corella Formation at the presently exposed crustal level, although some of the spread in the data may be due to a relatively small contribution from devolatilization reactions in the calc-silicates, or thermal fluctuations attending deformation and metamorphism. The overall L-shaped trend of the data on plots of δ13C vs. δ18O is most consistent with mixing of large volumes of externally derived fluids with small volumes of locally derived fluid produced by devolatilization of calc-silicate rocks. Localization of the vein systems in dilatant sites around metadolerite/calc-silicate boundaries indicates a strong structural control on fluid flow, and the stable isotope data suggest fluid migration must have occurred at scales greater than at least 1 km. The ultimate source for the external fluid is uncertain, but is probably fluid released from crystallizing melts derived from the lower crust or upper mantle. Intrusion of magmas below the exposed crustal level would also explain the high geothermal gradient calculated for the regional metamorphism.  相似文献   

13.
The Whitestone Anorthosite (WSA), located in the Central Gneiss Belt of the south-western Grenville Province, Ontario, exhibits a nearly concentric metamorphic envelope characterized by an increase in modal scapolite, hornblende, epidote and garnet, developed around a core of granulite facies clinopyroxene ± orthopyroxene ± garnet meta-anorthosite. Scapolite- and hornblende-bearing assemblages develop mainly at the expense of plagioclase and pyroxene within the envelope. Stable isotopic and petrological data for scapolite-bearing mineral assemblages within meta-anorthosite constrain the source of carbon responsible for CO3-scapolite formation and the extent of fluid/rock interaction between the anorthosite and adjacent lithologies. Stable isotopic data indicate increasing δ18O and δ13C from core to margin of the meta-anorthosite and for samples from the southern extension of the WSA, where it is ductilely deformed within the Parry Sound Shear Zone (PSSZ). The average δ18OSMOW value (whole rock) for the WSA core is 6.9‰, increasing to 11.5‰ where the WSA is in tectonic contact with marble breccia. The average δ13CPBD value of scapolite in meta-anorthosite from the centre of the WSA is -3.4‰, increasing to -0.5‰ at the eastern (marble) contact. Average values of δ13C for scapolite and whole-rock δ18O for samples from the shear zone are -1.0 and 8.0‰, respectively. Marbles have average δ18O and δ13C values of 19.2 and -0.4‰, respectively. The sulphate content of texturally primary scapolite decreases from the core of the WSA (XSO4= 0.48) to the eastern contact (≤0.05). Texturally late scapolite after plagioclase and garnet tends to be CO3-rich relative to texturally primary scapolite, and some scapolite grains show zoning in the anion site with CO3-enriched rims. Scapolite composition may vary at any scale from a single grain to outcrop. The pattern of isotopic enrichment in 13C and 18O preserved in the eastern margin of the WSA is consistent with marble as the major source of fluid contributing to the formation of the metamorphic envelope. The decrease in XSO4 and increase in XCO3 in scapolite toward the margin of the WSA indicate that the volatile content was reset by, or developed from, a CO2-bearing fluid. Assuming derivation of fluid from marble, minimum fluid/rock values at the margin of the WSA range from 0.03 for the least enriched, to 0.30 for the most isotopically enriched samples. Although marble is not found in immediate contact with samples of sheared meta-anorthosite from the PSSZ, a marble source is also consistent with the C and O isotope composition and anion chemistry of scapolite within these samples.  相似文献   

14.
The sedimentary record of carbonate carbon isotopes (δ13Ccarb) provides one of the best methods for correlating marine strata and understanding the long‐term evolution of the global carbon cycle. This work focuses on the Late Ordovician Guttenberg isotopic carbon excursion, a ca 2·5‰ positive δ13Ccarb excursion that is found in strata globally. Substantial variability in the apparent magnitude and stratigraphic morphology of the Guttenberg excursion at different localities has hampered high‐resolution correlations and led to divergent reconstructions of ocean chemistry and the biogeochemical carbon cycle. This work investigates the magnitude, spatial scale and sources of isotopic variability of the Guttenberg excursion in two sections from Missouri, USA. Centimetre‐scale isotope transects revealed variations in δ13Ccarb and δ18Ocarb greater than 2‰ across individual beds. Linear δ13Ccarb to δ18Ocarb mixing lines, together with petrographic and elemental abundance data, demonstrate that much of the isotopic scatter in single beds is due to mixing of isotopically distinct components. These patterns facilitated objective sample screening to determine the ‘least‐altered’ data. A δ18Ocarb filter based on empirical δ18Ocarb values of well‐preserved carbonate mudstones allowed further sample discrimination. The resulting ‘least‐altered’ δ13Ccarb profile improves the understanding of regional as well as continental‐scale stratigraphic relations in this interval. Correlations with other Laurentian sections strongly suggest that: (i) small‐scale variability in Guttenberg excursion δ13Ccarb values may result in part from local diagenetic overprinting; (ii) peak‐Guttenberg excursion δ13Ccarb values of the Midcontinent are not distinct from their Taconic equivalents; and (iii) no primary continental‐scale spatial gradient in δ13Ccarb (for example, arising from chemically distinct ‘aquafacies’) is required during Guttenberg excursion‐time. This study demonstrates the importance of detailed petrographic and geochemical screening of samples to be used for δ13Ccarb chemostratigraphy and for enhancing understanding of epeiric ocean chemistry.  相似文献   

15.
The stable carbon isotopic composition (expressed as δ13C) of herbivore remains is commonly used to reconstruct past changes in the relative abundance of C4 versus C3 grass biomass (C4 relative abundance). However, the strength of the relationship between herbivore δ13C and C4 relative abundance in extant ecosystems has not been thoroughly examined. We determined sources of variation in δ13C of bone collagen and tooth enamel of kangaroos (Macropus spp.) collected throughout Australia by measuring δ13C of bone collagen (779 individuals) and tooth enamel (694 individuals). An index of seasonal water availability, i.e. the distribution of rainfall in the C4 versus C3 growing seasons, was used as a proxy for C4 relative abundance, and this variable explained a large proportion of the variation in both collagen δ13C (68%) and enamel δ13C (68%). These figures increased to 78% and 77%, respectively, when differences between kangaroo species were accounted for. Vegetation characteristics, such as woodiness and the presence of an open forest canopy, had no effect on collagen or enamel δ13C. While there was no relationship between collagen δ13C and kangaroo age at death, tooth enamel produced later in life, following weaning, was enriched in 13C by 3.5‰ relative to enamel produced prior to weaning. From the observed relationships between seasonal water availability and collagen and enamel δ13C, enrichment factors (ε) for collagen-diet and enamel-diet (post-weaning) were estimated to be 5.2‰ ± 0.5 (95% CI) and 11.7‰ ± 0.6 (95% CI), respectively. The findings of this study confirm that at a continental scale, collagen and enamel δ13C of a group of large herbivores closely reflect C4 relative abundance. This validates a fundamental assumption underpinning the use of isotopic analysis of herbivore remains to reconstruct changes in C4 relative abundance.  相似文献   

16.
In order to characterize the oxygen isotopic composition of internal phosphate and explore the possibility of using these data to identify phosphate sources, we measured oxygen isotopic compositions of phosphate (δ18Op) in sediment pore water in Hongfeng Lake, a typical deep-water lake in a mountainous area. These data, in combination with δ18Op in surface water samples and water column samples, were successfully used to identify phosphate sources. The δ18Op value of sediment pore water ranged from 15.2‰ to 15.8‰, with an average value of 15.5‰—the δ18Op value of internal phosphate. The δ18Op values decreased gradually through the water column from 19.4‰ in surface water to 16.4‰ in deeper water, implying that internal phosphate had more negative δ18Op values than external phosphate. This finding was substantiated by horizontal variations in δ18OP values, which decreased with increasing distance from inflowing rivers. All collected evidence suggests that external and internal phosphate have distinctly different isotopic signatures and that these signatures have not been considerably altered by biological mediation in Hongfeng Lake. Therefore, δ18OP can be used to distinguish phosphate sources. A two-endmember mixing model showed that internal phosphate had an average contribution of 40%, highlighting the influence of internal phosphorus loading on aqueous phosphate and eutrophication. This study illustrates the need to reduce the internal phosphorus load from sediment and provides guidance for nutrient management and in-lake restoration treatment in Hongfeng Lake. The data presented here are limited, but serve to highlight the great potential of δ18Op as an effective tracer for identifying phosphate sources. Systematic investigations of the oxygen isotopic compositions of external phosphate, internal phosphate, and phosphate through the water column, in combination with in-lake P biogeochemical cycle study, would be desirable in further research.  相似文献   

17.
The Rb-Sr isochron age of igneous ankerite-calcite and siderite carbonatites in central Tuva is estimated at 118 ± 9 Ma. The following ranges of initial values of O, C, Sr, and sulfide and S isotopic compositions were established: δ18Ocarb = +(8.8?14.7)‰, δ13Ccarb = ?(3.6?4.9)‰, δ18Oquartz = +(11.6?13.7)‰, δ34Spyrite = +(0.3?1.1)‰, and (87Sr/86Sr)i =0.7042?0.7048 for ankerite-calcite carbonatite and δ18Osid = +(9.2?12.4)‰, δ13Csid = ?(3.9?5.9)‰, δ18Oquartz = +(11.2?11.4)‰, δ34Spyrite = ?(4.4–1.8)‰, δ34Ssulfate = +(8.6?14.5)‰, and (87Sr/86Sr)i = 0.7042?0.7045 for siderite carbonatite. The obtained isotopic characteristics indicate that both varieties of carbonatites are cognate and their mantle source is comparable with the sources of Late Mesozoic carbonatites in the western Transbaikal region and Mongolia. The revealed heterogeneity of isotopic compositions of carbonatites is caused by their contamination with country rocks, replacement with hydrothermal celestine, and supergene alteration.  相似文献   

18.
The geochemical and isotopic composition of surface waters and groundwater in the Velenje Basin, Slovenia, was investigated seasonally to determine the relationship between major aquifers and surface waters, water–rock reactions, relative ages of groundwater, and biogeochemical processes. Groundwater in the Triassic aquifer is dominated by HCO3 , Ca2+, Mg2+ and δ13CDIC indicating degradation of soil organic matter and dissolution of carbonate minerals, similar to surface waters. In addition, groundwater in the Triassic aquifer has δ18O and δD values that plot near surface waters on the local and global meteoric water lines, and detectable tritium, likely reflecting recent (<50 years) recharge. In contrast, groundwater in the Pliocene aquifers is enriched in Mg2+, Na+, Ca2+, K+, and Si, and has high alkalinity and δ13CDIC values, with low SO4 2– and NO3 concentrations. These waters have likely been influenced by sulfate reduction and microbial methanogenesis associated with coal seams and dissolution of feldspars and Mg-rich clay minerals. Pliocene aquifer waters are also depleted in 18O and 2H, and have 3H concentrations near the detection limit, suggesting these waters are older, had a different recharge source, and have not mixed extensively with groundwater in the Triassic aquifer.  相似文献   

19.
MIS 11 is often considered to be the best climatic analogue for the Holocene. Many studies have suggested, however, that it is a period of extreme climate warmth comparable in temperatures to the Middle and Late Pliocene. In Britain deposits of the Hoxnian interglacial are correlated to MIS 11 and multi-proxy techniques can be used to reconstruct the climate of this interglacial. Soil, groundwater and freshwater carbonates are common in Hoxnian deposits and the stable isotopic composition of these precipitates can be used to increase our understanding of MIS 11 environments in Britain. Carbonates from Marks Tey, Clacton, Swanscombe, Elveden and West Stow are studied, the stratigraphic context of which indicates that their formation is broadly synchronous (in the mid-Hoxnian, pollen zones Ho II to Ho III). The carbon isotopic composition of groundwater and pedogenic carbonates is typically depleted with respect to δ13C (ca −9 to −8‰ VPDB) reflecting uptake of plant respired CO2 during water migration/recharge. The carbon isotopic composition of lacustrine carbonate is more enriched with respect to δ13C (ca 0-1‰VPDB) reflecting the equilibration of lake waters with atmospheric CO2. The δ18O of groundwater and pedogenic carbonates is slightly more enriched than modern soil carbonates but not as enriched as soil carbonates formed under interglacials that were warmer than the Holocene (i.e. the Cromerian). The stable isotopic composition of Hoxnian carbonates does not, therefore, indicate that this interglacial was characterised by uniquely warm climates in the context of other Middle Pleistocene interglacials and the Holocene. This is contrary to many marine and littoral records from around the world but consistent with environmental records from Britain and Europe.  相似文献   

20.
Abstract Positive shifts in global seawater δ13CDIC are related to changes in the ratio of organic relative to inorganic carbon burial in oceanic basins, whereas factors such as climatic cooling and the accumulation of polar ice are known to cause positive shifts in δ18O. Here, an alternative model is proposed for the formation of local positive isotope shifts in shallow-marine settings. The model involves geochemically altered platform-top water masses and the effects of early meteoric diagenesis on carbonate isotopic composition. Both mechanisms are active on modern (sub)tropical carbonate platforms and result in low carbonate δ13C and δ18O relative to typical oceanic values. During high-amplitude transgressive events, the impact of isotopically light meteoric fluids on the carbonate geochemistry is much reduced, and 13C-depleted platform-top water mixes with open oceanic water masses having higher isotope values. Both factors are recorded as a transient increase in carbonate 13C and 18O relative to low background values. These processes must be taken into consideration when interpreting the geochemical record of ancient epeiric seas.  相似文献   

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