Origin and fate of organic carbon in the freshwater part of the Scheldt Estuary as traced by stable carbon isotope composition
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On the basis of proposing the existence of a karst carbon cycle and carbon sink at a watershed scale, this paper provides four pieces of evidence for the integration of geology and ecology during the carbon cycle processes in the karst dynamic system, and estimated the karst carbon sink effect using the methods of comparative monitoring of paired watersheds and the carbon stable isotope tracer technique. The results of the soil carbon cycle in Maocun, Guilin, showed that the soil carbon cycle in the karst area, the weathering and dissolution of carbonate rocks under the soil, resulted in a lower soil respiration of 25% in the karst area than in a non-karst area (sandstone and shale), and the carbon isotope results indicated that 13.46% of the heavy carbon of the limestone is involved in the soil carbon cycle. The comparative monitoring results in paired watersheds, suggesting that the HCO3- concentration in a karst spring is 10 times that of a rivulet in a non-karst area, while the concentration of inorganic carbon flux is 23.8 times. With both chemical stoichiometry and carbon stable isotopes, the proportion of carbon in karst springs derived from carbonate rocks was found to be 58.52% and 37.65% respectively. The comparison on carbon exchange and isotopes at the water-gas interface between the granite and carbonate rock basins in the Li River showed that the CO2 emission of the karst water is 10.92 times that of the allogenic water from the non-karst area, while the carbon isotope of HCO3- in karst water is lighter by 8.62‰. However, this does not mean that the karst water body has a larger carbon source effect. On the contrary, it means the karst water body has a greater karst carbon sink effect. When the karst subterranean stream in Zhaidi, Guilin, is exposed at the surface, carbon-rich karst water stimulated the growth of aquatic plants. The values of carbon stable isotopes in the same species of submerged plants gradually becomes heavier and heavier, and the 512 m flow process has a maximum range of 15.46‰. The calculation results showed that 12.52% of inorganic carbon is converted into organic carbon. According to the data that has been published, the global karst carbon sink flux was estimated to be 0.53-0.58 PgC/a, equivalent to 31.18%-34.41% of the global forest carbon sink flux. In the meanwhile, the karst carbon sink flux in China was calculated to be 0.051 PgC/a, accounting for 68% of its forest carbon sink flux.
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Abstract The beginning and end of the Proterozoic Eon are marked by extreme variations in carbonate carbon isotope values that have been interpreted to record massive perturbations to the global carbon cycle. The lower Proterozoic contains an extended interval of strata characterized by positive carbonate δ 13 C values. Conversely, uppermost Proterozoic carbonate strata contain thick intervals with extremely negative δ 13 C values and multiple large swings in carbonate δ 13 C. Previous attempts to model these pronounced carbon isotope excursions as shifts in the global marine dissolved inorganic carbon (DIC) reservoir have proved to be problematic, as the direction and magnitude of these positive and negative carbon isotope excursions require unrealistic amounts of either organic carbon burial or organic carbon oxidation, respectively. Here we present a modified global carbon cycle model—coupled with oxygen and sulfur cycle mass balances—that includes a parameterization of the recycling of sedimentary isotope anomalies and allows the extent of organic carbon oxidation to vary as a function of atmospheric oxygen levels. Our model is designed to match carbon isotope records while maintaining redox and mass balance with a given set of initial conditions and carbon cycle parameterizations. Using this approach, we demonstrate that there is a range of plausible biogeochemical perturbations that could induce substantial δ 13 C excursions in the global marine DIC reservoir. However, we also find that there are multiple, nonunique Earth system states for any observed marine δ 13 C value.
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The existence of unusually large fluctuations in the Neoproterozoic (1,000–543 million years ago) carbon-isotopic record implies strong perturbations to the Earth's carbon cycle. To analyze these fluctuations, we examine records of both the isotopic content of carbonate carbon and the fractionation between carbonate and marine organic carbon. Together, these are inconsistent with conventional, steady-state models of the carbon cycle. The records can be well understood, however, as deriving from the nonsteady dynamics of two reactive pools of carbon. The lack of a steady state is traced to an unusually large oceanic reservoir of organic carbon. We suggest that the most significant of the Neoproterozoic negative carbon-isotopic excursions resulted from increased remineralization of this reservoir. The terminal event, at the Proterozoic–Cambrian boundary, signals the final diminution of the reservoir, a process that was likely initiated by evolutionary innovations that increased export of organic matter to the deep sea.
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Over million-year timescales, the geologic cycling of carbon controls long-term climate and the oxidation of Earth's surface. Inferences about the carbon cycle can be made from time series of carbon isotopic ratios measured from sedimentary rocks. The foundational assumption for carbon isotope chemostratigraphy is that carbon isotope values reflect dissolved inorganic carbon in a well-mixed ocean in equilibrium with the atmosphere. However, when applied to shallow-water platform environments, where most ancient carbonates preserved in the geological record formed, recent research has documented the importance of considering both local variability in surface water chemistry and diagenesis. These findings demonstrate that carbon isotope chemostratigraphy of platform carbonate rarely represent the average carbonate sink or records changes in the composition of global seawater. Understanding what causes local variability in shallow-water settings, and what this variability might reveal about global boundary conditions, are vital questions for the next generation of carbon isotope chemostratigraphers.
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Over million-year timescales, the geologic cycling of carbon controls long-term climate and the oxidation of Earth's surface. Inferences about the carbon cycle can be made from time series of carbon isotopic ratios measured from sedimentary rocks. The foundational assumption for carbon isotope chemostratigraphy is that carbon isotope values reflect dissolved inorganic carbon in a well-mixed ocean in equilibrium with the atmosphere. However, when applied to shallow-water platform environments, where most ancient carbonates preserved in the geological record formed, recent research has documented the importance of considering both local variability in surface water chemistry and diagenesis. These findings demonstrate that carbon isotope chemostratigraphy of platform carbonate rarely represent the average carbonate sink or directly records changes in the composition of global seawater. Understanding what causes local variability in shallow-water settings, and what this variability might reveal about global boundary conditions, are vital questions for the next generation of carbon isotope chemostratigraphers.
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Significance The Central Atlantic magmatic province (CAMP) is coincident with the end-Triassic extinction event and several negative carbon isotope excursions (CIEs). Sill emplacements in Brazil would have generated extensive volatiles and degassing due to the contact metamorphism of evaporites, organic-rich shales, and hydrocarbons. Thermogenic carbon release from contact metamorphism represents a plausible source for 12 C; however, this has not yet been explored from a carbon cycle approach. This study explores the effects of thermogenic carbon release from CAMP using carbon cycle modeling and shows that it represents a credible source for the negative CIEs at the end-Triassic. It strengthens the hypothesis that the subvolcanic part of a large igneous province is of major importance for understanding carbon cycle disruptions.
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Significance The end-Triassic mass extinction that occurred ∼202 Ma is one of the “Big Five” biotic crises of the Phanerozoic Eon. It is also accompanied by an organic carbon isotopic excursion that has long been interpreted as the result of a global-scale carbon-cycle disruption. Rather than being due to massive inputs of exogenous light carbon into the ocean–atmosphere system, the isotopic excursion is shown here to reflect regional sea-level change that caused a transition from a marine ecosystem to a less saline, shallow-water, microbial-mat environment and resultant changes in the sources of organic matter. The mass extinction that occurred slightly later, caused by abrupt injection of volcanogenic CO 2 , is accompanied by only modest changes in organic carbon isotopic composition.
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Abstract The emplacement of the Karoo Large Igneous Province (LIP) occurred synchronously with the Toarcian crisis (ca. 183 Ma), which is characterized by major carbon cycle perturbations. A marked increase in the atmospheric concentration of CO 2 ( p CO 2 ) attests to significant input of carbon, while negative carbon isotope excursions (CIEs) in marine and terrestrial records suggest the involvement of a 12 C-enriched source. Here we explore the effects of pulsed carbon release from the Karoo LIP on atmospheric p CO 2 and δ 13 C of marine sediments, using the GEOCLIM carbon cycle model. We show that a total of 20,500 Gt C replicates the Toarcian p CO 2 and δ 13 C proxy data, and that thermogenic carbon (δ 13 C of −36 ‰) represents a plausible source for the observed negative CIEs. Importantly, an extremely isotopically depleted carbon source, such as methane clathrates, is not required in order to replicate the negative CIEs. Although exact values of individual degassing pulses represent estimates, we consider our emission scenario realistic as it incorporates the available geological knowledge of the Karoo LIP and a representative framework for Earth system processes during the Toarcian.
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