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1.
The origin and the chemical and isotopic evolution of dissolved inorganic carbon (DIC) in groundwater of the Okavango Delta in semi-arid Botswana were investigated using DIC and major ion concentrations and stable oxygen, hydrogen and carbon isotopes (δD, δ18O and δ13CDIC). The δD and δ18O indicated that groundwater was recharged by evaporated river water and unevaporated rain. The river water and shallow (<10 m) groundwater are Ca–Na–HCO3 type and the deep (≥10 m) groundwater is Na–K–HCO3 to HCO3–Cl–SO4 to Cl–SO4–HCO3. Compared to river water, the mean DIC concentrations were 2 times higher in shallow groundwater, 7 times higher in deep groundwater and 24 times higher in island groundwater. The δ13CDIC indicate that DIC production in groundwater is from organic matter oxidation and in island groundwater from organic matter oxidation and dissolution of sodium carbonate salts. The ionic and isotopic evolution of the groundwater relative to evaporated river water indicates two independent pools of DIC.  相似文献   

2.
The impact of landfill contaminated groundwater along a reach of a small stream adjacent to a municipal landfill was investigated using stable carbon isotopes as a tracer. Groundwater below the stream channel, groundwater seeping into the stream, groundwater from the stream banks and stream water were sampled and analysed for dissolved inorganic carbon (DIC) and the isotope ratio of DIC (δ13CDIC). Representative samples of groundwater seeping into the stream were collected using a device (a ‘seepage well’) specifically designed for collecting samples of groundwater seeping into shallow streams with soft sediments. The DIC and δ13CDIC of water samples ranged from 52 to 205 mg C/L and ?16·9 to +5·7‰ relative to VPDB standard, respectively. Groundwater from the stream bank adjacent to the landfill and some samples of groundwater below the stream channel and seepage into the stream showed evidence of δ13C enriched DIC (δ13CDIC = ?2·3 to +5·7‰), which we attribute to landfill impact. Stream water and groundwater from the stream bank opposite the landfill did not show evidence of landfill carbon (δ13CDIC = ?10·0 to ?16·9‰). A simple mixing model using DIC and δ13CDIC showed that groundwater below the stream and groundwater seeping into the stream could be described as a mixture of groundwater with a landfill carbon signature and uncontaminated groundwater. This study suggests that the hyporheic zone at the stream–groundwater interface probably was impacted by landfill contaminated groundwater and may have significant ecological implications for this ecotone. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

3.
The coastal confined aquifer in the Gulf of Urabá (Colombia) is an important water source for the banana agro‐industry as well as for urban and rural communities. However, the main processes controlling recharge and mixing in the aquifer are still poorly understood. Hydrochemical analyses and stable isotope monitoring were conducted to (a) determine groundwater recharge origin, mean groundwater age, and the main processes governing groundwater chemistry and the potential mixing of marine water and the influence of diffusive processes from the two surrounding aquitard layers. Hydrochemical data indicate that the main processes affecting the dissolved chemical composition include cation exchange, dissolution of carbonated and CO2, and silicate weathering. δ18O and δ2H compositions combined with 14C data highlight the differences in climatic conditions between the recharge zone and the confined section of the aquifer, which is close to the Atlantic Ocean. Groundwater samples with 14C ages from recent to 28,300 years BP show a depleted isotopic trend ranging from ?6.43‰ to ?9.14‰ in δ18O and from ?43.2‰ to ?65.7‰ in δ2H. The most depleted δ18O and δ2H compositions suggest a cooler recharge climate than the current conditions (corresponding to the last glacial period of the late Pleistocene). Depleted δ13C values in the total dissolved inorganic carbon indicate the existence of organic material oxidation processes within the geologic formation. These results can be used or transferred to enhance groundwater modelling efforts in other confined coastal aquifers of South America where scarcity of long‐term monitoring data limits water resources planification under a changing climate.  相似文献   

4.
13C/12C- and 18O/16O-signatures of Calcite Precipitations in Drainage Systems Measurements of drainage waters show two distinct processes of calcite precipitation: 1. reprecipitation of calcium carbonate previously dissolved in groundwaters and 2. absorption of atmospheric CO2 by alkaline solutions. Both processes may be distinguished by the stable isotopes of oxygen and carbon. Calcite precipitated from carbonate groundwater yields δ13C ≈ ?13%0 (PDB) and δ18O ≈ 24%0 (SMOW), whereas calcite produced by CO2-absorption shows δ13C ≈ ?25%0 (PDB) and δ18O ≈ 10%0 (SMOW).  相似文献   

5.
We measured the concentrations of dissolved inorganic carbon (DIC) and major ions and the stable carbon isotope ratios of DIC (δ13CDIC) in two creeks discharging from carbonate‐rich sulphide‐containing mine tailings piles. Our aim was to assess downstream carbon evolution of the tailings discharge as it interacted with the atmosphere. The discharge had pH of 6.5–8.1 and was saturated with respect to carbonates. Over the reach of one creek, the DIC concentrations decreased by 1.1 mmol C/l and δ13CDIC increased by ~4.0‰ 200 m from the seep source. The decrease in the DIC concentrations was concomitant with decreases in the partial pressure of CO2(aq) because of the loss of excess CO2(aq) from the discharge. The corresponding enrichment in the δ13CDIC is because of kinetic isotope fractionation accompanying the loss of CO2(g). Over the reach of the other creek, there was no significant decrease in the DIC concentrations or notable changes in the δ13CDIC. The insignificant change in the DIC concentrations and the δ13CDIC is because the first water sample was collected 160 m away from the discharge seep, not accessible during this research. In this case, most of the excess CO2(aq) was lost before our first sampling station. Our results indicate that neutral discharges from tailings piles quickly lose excess CO2(aq) to the atmosphere and the DIC becomes enrich in 13C. We suggest that a significant amount of carbon cycling in neutral discharges from tailings piles occur close to the locations where the discharge seeps to the surface. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

6.
The Nyangqu River, the largest right bank tributary of the Yarlung Zangbo River in the Qinghai–Tibet Plateau, was representative of an alpine riverine carbon cycle experiencing climate change. In this study, dissolved inorganic carbon (DIC) spatial and seasonal variations, as well as their carbon isotopic compositions (δ13CDIC) in river water and groundwater were systematically investigated to provide constraints on DIC sources, recharge and cycling. Significant changes in the δ13CDIC values (from −2.9‰ to −23.4‰) of the water samples were considered to be the result of different contributions of two dominant DIC origins: soil CO2 dissolution and carbonate weathering. Three types of rock weathering (dissolution of carbonate minerals by H2CO3 and H2SO4, and silicate dissolution by H2CO3) were found to control the DIC input into the riverine system. In DIC cycling, groundwater played a significant role in delivering DIC to the surface water, and DIC supply from tributaries to the main stream increased from the dry season to the wet season. Notably, the depleted δ13CDIC ‘peak’ around the 88.9° longitude, especially in the September groundwater samples, indicated the presence of ‘special’ DIC, which was attributed to the oxidation of methane from the Jiangsa wetland located nearby. This wetland could provide large amounts of soil organic matter available for bacterial degradation, producing 13C-depleted methane. Our study provided insights regarding the role of wetlands in riverine carbon cycles and highlighted the contribution of groundwater to alpine riverine DIC cycles.  相似文献   

7.
The stable isotopic composition of dissolved inorganic carbon (δ13C‐DIC) was investigated as a potential tracer of streamflow generation processes at the Sleepers River Research Watershed, Vermont, USA. Downstream sampling showed δ13C‐DIC increased between 3–5‰ from the stream source to the outlet weir approximately 0·5 km downstream, concomitant with increasing pH and decreasing PCO2. An increase in δ13C‐DIC of 2·4 ± 0·1‰ per log unit decrease of excess PCO2 (stream PCO2 normalized to atmospheric PCO2) was observed from downstream transect data collected during snowmelt. Isotopic fractionation of DIC due to CO2 outgassing rather than exchange with atmospheric CO2 may be the primary cause of increased δ13C‐DIC values downstream when PCO2 of surface freshwater exceeds twice the atmospheric CO2 concentration. Although CO2 outgassing caused a general increase in stream δ13C‐DIC values, points of localized groundwater seepage into the stream were identified by decreases in δ13C‐DIC and increases in DIC concentration of the stream water superimposed upon the general downstream trend. In addition, comparison between snowmelt, early spring and summer seasons showed that DIC is flushed from shallow groundwater flowpaths during snowmelt and is replaced by a greater proportion of DIC derived from soil CO2 during the early spring growing season. Thus, in spite of effects from CO2 outgassing, δ13C of DIC can be a useful indicator of groundwater additions to headwater streams and a tracer of carbon dynamics in catchments. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

8.
A recently developed approach to carbon isotope methodology (process recognition via isotope diagrams) is applied in a multidisciplinary study of precipitation‐recharged aquifers of the lowlands–plains area of the Manawatu (south‐west North Island). Urban and rural areas rely on groundwater from the upper levels of a deep basin sequence comprising marine and terrestrial sediments of Pleistocene age. Hydrochemical and isotopic (18O, 3H, 13C and 14C) data are merged with known details of geology and hydrogeology to reveal two separate confined aquifers within the depth range to 200 m. The shallower of these, below unconfined, locally recharged groundwater, is recharged on the foothills of the Ruahine Range to the north‐east of the study area; flow direction is NE–SW. The deeper confined aquifer is recharged on the Tararua Range to the immediate east; flow direction essentially is transverse (SE–NW) to that in the shallower aquifer. Two processes are identified as dominant contributors to concentration and isotopic composition of dissolved inorganic carbon (DIC), namely addition of CO2 from decay of organic materials and carbonate dissolution. Limitations of carbon isotope methods in determining residence times are illustrated by the data. Although the confined groundwater is essentially tritium‐free, only a few samples showed conclusive evidence of significant ageing on the time‐scale of 14C. Copyright © 2001 John Wiley & Sons, Ltd.  相似文献   

9.
Waterborne carbon (C) export from terrestrial ecosystems is a potentially important flux for the net catchment C balance and links the biogeochemical C cycling of terrestrial ecosystems to their downstream aquatic ecosystems. We have monitored hydrology and stream chemistry over 3 years in ten nested catchments (0.6–15.1 km2) with variable peatland cover (0%–22%) and groundwater influence in subarctic Sweden. Total waterborne C export, including dissolved and particulate organic carbon (DOC and POC) and dissolved inorganic carbon (DIC), ranged between 2.8 and 7.3 g m–2 year–1, representing ~10%–30% of catchment net ecosystem exchange of CO2. Several characteristics of catchment waterborne C export were affected by interacting effects of peatland cover and groundwater influence, including magnitude and timing, partitioning into DOC, POC, and DIC and chemical composition of the exported DOC. Waterborne C export was greater during the wetter years, equivalent to an average change in export of ~2 g m–2 year–1 per 100 mm of precipitation. Wetter years led to a greater relative increase in DIC export than DOC export due to an inferred relative shift in dominance from shallow organic flow pathways to groundwater sources. Indices of DOC composition (SUVA254 and a250/a365) indicated that DOC aromaticity and average molecular weight increased with catchment peatland cover and decreased with increased groundwater influence. Our results provide examples on how waterborne C export and DOC composition might be affected by climate change. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

10.
Increasing groundwater salinity and depletion of the aquifers are major concerns in the UAE. Isotopes of oxygen, hydrogen, and carbon concentrations in groundwater were used to estimate evaporation loss using the isotopes of oxygen and hydrogen, and using a carbon isotope to trace inorganic carbon cycling in two main aquifers in the eastern part of the United Arab Emirates. The δD‐δ18O of groundwater samples plotted on a line given by: δD = 4 δ18O + 4 ·4 (r2 = 0·4). In comparison, the local meteoric water line (LMWL) has been defined by the line: δD = 8 δ18O + 15. In order to better understand the system investigated, samples were separated into two groups based on the δD‐δ18O relationship. These are (1) samples that plot above the LMWL (δD = 6·1 δ18O + 12·4, r2 = 0·8) and which are located predominantly in the north of the study area, and (2) samples that plot below the LMWL (δD = 5·6 δ18O + 6·2, r2 = 0·8) and which are mostly distributed in the south. Slopes for both the groups are similar and lower than that for LMWL indicating potential evaporation of recharging water. However, the y‐intercept, which differs between the two groups, suggests evaporation of return flow and evapotranspiration in the unsaturated zone to be more significant in the south. This is attributed to intense agricultural activities in the region. Samples from the eastern Gravel Plain aquifer have δ13C and dissolved inorganic carbon (DIC) values in the range from ? 10 to 17‰, and 12–100 mg C/l, respectively, while the range for those from the Ophiolite aquifer is from ? 11 to ? 16.4‰, and 16–114 mg C/l respectively. This suggests the control of C‐3 and C‐4 plants on DIC formation, an observation supported by the range δ13C of soil organic matter (from ? 18·5 to ? 22·1‰.) Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

11.
Increases in calcite deposition rates combined with decreases in δ13C and δ18O in three modern stalagmites from Brown's Folly Mine, Wiltshire, England, are correlative with a well-documented re-vegetation above the mine. Increased soil PCO2 resulted in greater amounts of dissolved CaCO3 in the drip waters, which consequently increased annual calcite deposition rates. The absence of deposition prior to 1916 (28 years after the mine was closed) indicates that vegetation had not yet sufficiently developed to allow higher PCO2 values to form in the soil. Lower δ13C values through time may reflect the increased input of isotopically light biogenic carbon to the total dissolved inorganic carbon (DIC). δ18O decreased synchronously with δ13C, reflecting the increased importance of isotopically light winter recharge due to greater biomass-induced summer evapotranspiration. This is the first empirical demonstration that vegetation density can control stalagmite growth rates, δ13C, and δ18O, contributing critical insights into the interpretation of these climate proxies in ancient stalagmites.  相似文献   

12.
Understanding the carbon cycle of the Han River system in Korea is of prime interest in managing and preserving this valuable water resource for more than 20 million residents in the area. As a part of a comprehensive carbon cycling study for the Han River system, this report focuses on the carbon isotope compositions of dissolved inorganic carbon (DIC) in its two major tributaries, the North and the South Han Rivers. The major difference in carbonate chemistry of the tributaries originates primarily from the lithology of the catchment areas. The South Han River, draining a carbonate‐dominant terrain, has much higher alkalinities and DIC concentrations, whereas the lower concentrations in the North Han River indicate little influence of carbonate weathering. Likewise, δ13CDIC values in the South Han River indicate that the DIC input from the carbonate rocks is important in controlling carbon isotope ratios of DIC. For the North Han River, the oxidation of organic material influences the amount of riverine DIC and δ13CDIC values to a greater extent. Overall, remarkable seasonal and spatial variations of river chemistry and carbon isotope compositions of DIC reflect the variability in geo‐hydrologic characteristics, in the water regime, and in metabolic activities in the river water and/or the drainage areas. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

13.
Rivers, representing the primary conduits of dissolved inorganic carbon (DIC) from the continents to the oceans, are important components to the global carbon cycle. To better understand the complex carbon cycling dynamics within two nested, mixed lithology watersheds, two sites were studied along the karst influenced upper Green River in south‐central Kentucky, USA. Weekly samples were collected from June 2013 through May 2014 and analyzed for δ13CDIC. The mixing model IsoSource was employed to better understand source partitioning differences over seasonal time spans and across the two nested basins. In both the lithologically mixed upstream basin (53% carbonate rocks, 47% siliciclastic) and carbonate rock dominated downstream basin (96% carbonate rocks in the drainage area between Greensburg and Munfordville, 78% in the total area upstream from Munfordville), DIC was primarily derived from soil respiration. The proportion of DIC from dissolved carbonate minerals derived from the downstream carbonate rock dominated basin was similar to the upstream basin, due to carbonate mineral dissolution having such a consistent effect on the overall DIC content of the river. Seasonally, soil respiration provided the most DIC from fall to winter. Early spring precipitation, combined with limited seasonal photosynthesis, shifted groundwater to be the primary source of DIC, bringing in a flush of carbonate mineral‐rich water during higher flows. This study provides insight into carbon dynamics across multiple lithologies and the important influence of seasonality using carbon isotope sourcing to determine carbonate mineral dissolution variability and aid in understanding its contribution to global carbon flux quantification. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

14.
The Taho Formation in western Shikoku Island, Japan, consists of Triassic carbonates that formed on a seamount in the Panthalassic Ocean. In order to investigate the stratigraphy and paleoceanography of this carbonate succession, we analyzed the biostratigraphy and chemostratigraphy of a 17.6 m-thick section of the upper Taho Formation at the stratotype area in Tahokamigumi, Seiyo City. This section comprises bioclastic limestone containing Triassic bivalves, ammonoids, and conodonts. We recognized six conodont zones (in ascending order): the Novispathodus pingdingshanensis, Novispathodus brevissimus, Triassospathodus symmetricus, Triassospathodus homeri, Chiosella timorensis, and Magnigondolella cf. alexanderi zones. Thus, the studied carbonate succession is latest Smithian to Aegean in age. A δ13C profile of this section shows elevated values during the lowest Spathian followed by a gradual negative excursion, a subsequent positive excursion near the Spathian–Aegean boundary, and relatively constant values during the Aegean. The characteristic series of negative and positive excursions correlates with other δ13C records for this period, including the peak of the upper Smithian–lowest Spathian positive excursion (P3), lower to middle Spathian negative excursion (N4), and middle Spathian–lowest Aegean positive excursion (P4). This represents a new high-resolution Spathian–Aegean δ13C record of the Panthalassic Ocean, for which ages are constrained by conodont biostratigraphy. The Taho δ13C profile exhibits a consistent positive offset of ~2 ‰ as compared with those from other regions (i.e., mostly in the Tethyan Ocean). This can be explained by preferential removal of 12C from seawater during photosynthesis and calcification by marine organisms over the platform, and/or the relatively high δ13C values of dissolved inorganic carbon in the Panthalassic Ocean due to less influence of 12C-enriched terrestrial waters and high marine organic production/burial as compared with the more restricted Tethyan Ocean.  相似文献   

15.
Aquatic plants are essential for maintaining the diversity and stability of a lake ecosystem. Stable carbon isotopes (δ13C) of macrophytes have been widely used as a powerful tool to study ecological processes and paleoenvironmental evolution in lakes. Varying results are obtained when using the δ13C of macrophytes to study the changes in the lake environment at different spatio-temporal scales. Thus, sample preparation and subsequent laboratory analyses are crucial for studying environmental changes using the isotopic signal retained in the macrophytes, and are essential for the interpretation of isotope-environment relationships. This study analyzed the δ13C of different tissue components of macrophytes in three lakes of the lower Yangtze River basin, and a correlation analysis was performed on aquatic environments influencing the δ13C values in the different tissue components of macrophytes. The test results showed the difference between the δ13C values of the whole sample and cellulose. Relative analyses indicated that the major factors contributing to the δ13C variability in macrophytes were pH and the concentration of dissolved inorganic carbon (DIC). The δ13C of α-cellulose (δ13CAC) is more sensitive to environmental variables than that of the whole sample (δ13CW) and holocellulose (δ13CHC). The results of this study imply that extraction of α-cellulose is a prerequisite for research on the changes in lake environment using δ13C of macrophytes. This study aims to provide theoretical and data basis for further research on the environmental and ecological change using stable carbon isotopes of aquatic plants.  相似文献   

16.
Sedimentological and hydrogeological studies are combined in order to investigate the environmental conditions of the lacustrine sedimentation during the Holocene in Gallocanta Lake in Spain. Six units have been identified in the sedimentary succession, based on sedimentological facies and mineralogy, and three depositional stages have been defined: (1) alluvial, (2) carbonate lake system, (3) ephemeral carbonate–saline lake system. The transition between stages 2 and 3 implies a reduction in water inflows to the lake. The δ13C isotopical analysis of dolomites points to decaying organic matter as a source of carbon for the dissolved inorganic carbon and evinces that the δ13C variations in the lake were probably controlled by organic processes. On the other hand, δ18O values could be controlled by modifications in the hydrological system and not necessarily by climatic changes. In this sense, from the hydrological study, three aquifers can be defined: Triassic, Jurassic–Cretaceous and Cenozoic aquifers. The lack of coincidence between the surface and subterranean watershed suggests that the transition between the second and third stages is controlled by a shift of the subterranean watershed. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

17.
Geochemical and 13C/12C-isotopical Investigation of Mineral Waters in Northern Hessia (Germany) and the Origin of their CO2 Content The dissolved carbonate originates from three sources: 1. biogenetic soil-CO2, 2. volcanic CO2 related to the evaporites of the Zechstein formation, and 3. carbonate derived from the dissolution of limestones and dolomites. Miocenic basaltic melts penetrated the evaporites of the Zechstein, and the related CO2 was trapped in the intra- and intergranulars of the salt minerals. Circulating meteoric waters dissolve the salt minerals releasing CO2 gas. Thus, the occurrence of basalt is related to the CO2 contents of the evaporites, and the dissolution of only small amounts of salts rich in CO2 may result in a high concentration of carbonic acid. In waters rich in carbonate, where volcanic CO2 dominates over the other two sources of carbon, a δ13C-value of “salt-CO2” of about –1‰ (PDB) is obtained. Water with less dissolved carbonate species have smaller quantities of salt-CO2 down to about 20%.  相似文献   

18.
Dissolved inorganic carbon isotope (δ13CDIC) is an important tool to reveal the carbon cycle in lake systems. However, there are only few studies focusing on the spatial variation of δ13CDIC of closed lakes. Here we analyze the characteristics of δ13CDIC of 24 sampled lakes (mainly closed lakes) across the Qiangtang Plateau (QTP) and identify the driving factors for its spatial variation. The δ13CDIC value of these observed lakes varies in the range of ? 15·0 to 3·2‰, with an average value of ? 1·2‰. The δ13CDIC value of closed lakes is close to the atmospheric isotopic equilibrium value, much higher than that in rivers and freshwater lakes reported before. The high δ13CDIC value of closed lakes is mainly attributed to the significant contribution of carbonate weathering in the catchment and the evasion of dissolved CO2 induced by the strong evaporation of lake water. The δ13CDIC value of closed lakes has a logarithmic correlation with water chemistry (TDS, DIC and pCO2), also suggesting that the evapo‐concentration of lake water can influence the δ13CDIC value. The δ13CDIC value shows two opposite logarithmic correlations with lake size depending on the δ13CDIC range. This study suggests that the δ13C in carbonates in lacustrine sediments can be taken as an indicator of lake volume variation in closed lakes on QTP. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

19.
Uptake of atmospheric CO2 during sample collection and analysis, and consequent lowering of estimated ages, has rarely been considered in radiocarbon dating of groundwater. Using field and laboratory experiments, we show that atmospheric CO2 can be easily and rapidly absorbed in hyperalkaline solutions used for the extraction of dissolved inorganic carbon, resulting in elevated 14C measurements. Kinetic isotope fractionation during atmospheric CO2 uptake may also result in decrease of δ13C, leading to insufficient corrections for addition of dead carbon by geochemical processes. Consequently, measured 14C values of groundwater should not be used for age estimation without corresponding δ13C values, and historical 14C data in the range of 1 to 10% modern Carbon should be re‐evaluated to ensure that samples with atmospheric contamination are recognized appropriately. We recommend that samples for 14C analysis should be collected and processed in the field and the laboratory without exposure to the atmosphere. These precautions are considered necessary even if 14C measurements are made with an accelerator mass spectrometer.  相似文献   

20.
Immediately before the extinction of the end‐Guadalupian (Middle Permian; ca 260 Ma), a significant change to the global carbon cycle occurred in the superocean Panthalassa, as indicated by a prominent positive δ13C excursion called the Kamura event. However, the causes of this event and its connection to the major extinction of marine invertebrates remain unclear. To understand the mutual relationships between these changes, we analyzed the sulfur isotope ratio of the carbonate‐associated sulfate (CAS) and HCl‐insoluble residue, as well as the carbon isotope ratio of bulk organic matter, for the Middle‐Upper Permian carbonates of an accreted mid‐oceanic paleo‐atoll complex from Japan, where the Kamura event was first documented. We detected the following unique aspects of the stable carbon and sulfur isotope records. First, the extremely high δ13C values of carbonate (δ13Ccarb) over +5 ‰ during the Capitanian (late Guadalupian) were associated with large isotopic differences between carbonate and organic matter (Δ13C = δ13Ccarb ? δ13Corg). We infer that the Capitanian Kamura event reflected an unusually large amount of dissolved organic matter in the expanded oxygen minimum zone at mid‐depth. Second, the δ34S values of CAS (δ34SCAS) were inversely correlated with the δ13Ccarb values during the Capitanian to early Wuchiapingian (early Late Permian) interval. The Capitanian trend may have appeared under increased oceanic sulfate conditions, which were accelerated by intense volcanic outgassing. Bacterial sulfate reduction with increased sulfate concentrations in seawater may have stimulated the production of pyrite that may have incorporated iron in pre‐existing iron hydroxide/oxide. This stimulated phosphorus release, which enhanced organic matter production and resulted in high δ13Ccarb. Low δ34SCAS values under high sulfate concentrations were maintained and the continuous supply of sulfate cannot by explained only by the volcanic eruption of the Emeishan Trap, which has been proposed as a cause of the extinction. The Wuchiapingian δ34SCAS–δ13Ccarb correlation, likely related to low sulfate concentration, may have been caused by the removal of oceanic sulfate through the massive evaporite deposition.  相似文献   

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