17 research outputs found

    Enhanced Organic Carbon Burial in Sediments of Oxygen Minimum Zones Upon Ocean Deoxygenation

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    Oxygen minimum zones (OMZs) in the ocean are expanding. This expansion is attributed to global warming and may continue over the next 10 to 100 kyrs due to multiple climate CO2-driven factors. The expansion of oxygen-deficient waters has the potential to enhance organic carbon burial in marine sediments, thereby providing a negative feedback on global warming. Here, we study the response of dissolved oxygen in the ocean to increased phosphorus and iron inputs due to CO2-driven enhanced weathering and increased dust emissions, respectively. We use an ocean biogeochemical model coupled to a general ocean circulation model (the Hamburg Oceanic Carbon Cycle model, HAMOCC 2.0) to assess the impact of such regional deoxygenation on organic carbon burial in the modern ocean on time scales of up to 200 kyrs. We find that an increase in input of phosphorus and iron leads to an expansion of the area of the OMZ impinging on continental margin sediments and a significant decline in bottom water oxygen in the open ocean relative to pre-industrial conditions. The associated increase in organic carbon burial could contribute to the drawdown of ~1,600 Gt of carbon, which is equivalent to the total amount of CO2 in the atmosphere predicted for the year 2100 in a business as usual scenario, on time scales of up to 50 kyrs. The corresponding areal extent of sediments overlain by bottom waters with little or no oxygen as estimated by the model is not very different from the minimum area estimated for two major oceanic anoxic events in Earth's past. Such events were associated with major perturbations of the oceanic carbon cycle, including high rates of organic carbon burial. We conclude that organic carbon burial in low oxygen areas in the ocean could contribute to removal of anthropogenic CO2 from the atmosphere on long time scales

    Enhanced Organic Carbon Burial in Sediments of Oxygen Minimum Zones Upon Ocean Deoxygenation

    No full text
    Oxygen minimum zones (OMZs) in the ocean are expanding. This expansion is attributed to global warming and may continue over the next 10 to 100 kyrs due to multiple climate CO2-driven factors. The expansion of oxygen-deficient waters has the potential to enhance organic carbon burial in marine sediments, thereby providing a negative feedback on global warming. Here, we study the response of dissolved oxygen in the ocean to increased phosphorus and iron inputs due to CO2-driven enhanced weathering and increased dust emissions, respectively. We use an ocean biogeochemical model coupled to a general ocean circulation model (the Hamburg Oceanic Carbon Cycle model, HAMOCC 2.0) to assess the impact of such regional deoxygenation on organic carbon burial in the modern ocean on time scales of up to 200 kyrs. We find that an increase in input of phosphorus and iron leads to an expansion of the area of the OMZ impinging on continental margin sediments and a significant decline in bottom water oxygen in the open ocean relative to pre-industrial conditions. The associated increase in organic carbon burial could contribute to the drawdown of ~1,600 Gt of carbon, which is equivalent to the total amount of CO2 in the atmosphere predicted for the year 2100 in a business as usual scenario, on time scales of up to 50 kyrs. The corresponding areal extent of sediments overlain by bottom waters with little or no oxygen as estimated by the model is not very different from the minimum area estimated for two major oceanic anoxic events in Earth's past. Such events were associated with major perturbations of the oceanic carbon cycle, including high rates of organic carbon burial. We conclude that organic carbon burial in low oxygen areas in the ocean could contribute to removal of anthropogenic CO2 from the atmosphere on long time scales

    Nitrogen isotopes of bulk sediments for OAE2 samples

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    Sediment records of the stable isotopic composition of N (d15N) show light d15N values at several sites in the proto-North Atlantic during Oceanic Anoxic Event 2 (OAE 2) at the Cenomanian-Turonian transition (~94 Ma). The low d15N during the event is generally attributed to an increase in N2-fixation and incomplete uptake of ammonium for phytoplankton growth. A compilation of all reliable data for the proto North-Atlantic during OAE 2 demonstrates that the most pronounced negative shift in d15N from pre-OAE 2 to OAE 2 occurs in the open ocean, but with d15N never lower than -3 ppm. Using a box model of N cycling for the proto-North Atlantic during OAE 2, we show that N2-fixation is a major contributor to the d15N signal, especially in the open ocean. Incomplete uptake of ammonium for phytoplankton growth is important in regions dominated by downwelling, with lateral transport of ammonium acting as a major source. In the southern proto-North Atlantic, where bottom waters were euxinic, the light d15N signature is largely explained by upwelling of ammonium . Our study provides an overview of regional differences in d15N in the proto-North Atlantic and highlights the role of lateral exchange of water and nutrients, in addition to local biogeochemical processes, in determining d15N values of OAE 2 sediments

    Biogeochemical redox proxies in sediments from Yorkshire (UK), Schandelah (N Germany) and Dotternhausen (S Germany) during the Toarcian (Early Jurassic)

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    The data set includes Toarcian sedimentary records of total organic carbon contents and elemental concentrations of phosphorus, aluminium, iron, molybdenum, manganese, sulphur, vanadium and copper at 3 sites in the northern European Epicontinental Shelf (Yorkshire, Schandelah and Dotternhausen). It span the Toarcian Ocean Anoxic Event (T-OAE), including the onset and termination
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