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  • Copernicus  (2)
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  • 1
    Publication Date: 2020-04-30
    Description: The terrestrial subsurface is the largest source of freshwater globally. The organic carbon contained within it and processes controlling its concentration remain largely unknown. The global median concentration of dissolved organic carbon (DOC) in groundwater is low compared to surface waters, suggesting significant processing in the subsurface. Yet the processes that remove this DOC in groundwater are not fully understood. The purpose of this study was to investigate the different sources and processes influencing DOC in a shallow anoxic coastal aquifer. Uniquely, this study combines liquid chromatography organic carbon detection with organic (δ13CDOC) carbon isotope geochemical analyses to fingerprint the various DOC sources that influence the concentration, carbon isotopic composition, and character with respect to distance from surface water sources, depth below surface, and inferred groundwater residence time (using 3H activities) in groundwater. It was found that the average groundwater DOC concentration was 5 times higher (5 mg L−1) than the global median concentration and that the concentration doubled with depth at our site, but the chromatographic character did not change significantly. The anoxic saturated conditions of the aquifer limited the rate of organic matter processing, leading to enhanced preservation and storage of the DOC sources from peats and palaeosols contained within the aquifer. All groundwater samples were more aromatic for their molecular weight in comparison to other lakes, rivers and surface marine samples studied. The destabilization or changes in hydrology, whether by anthropogenic or natural processes, could lead to the flux of up to 10 times more unreacted organic carbon from this coastal aquifer compared to deeper inland aquifers.
    Print ISSN: 1027-5606
    Electronic ISSN: 1607-7938
    Topics: Geography , Geosciences
    Published by Copernicus on behalf of European Geosciences Union.
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  • 2
    Publication Date: 2019-02-12
    Description: The terrestrial sub-surface is the largest source of freshwater globally. The organic carbon contained within it and processes controlling its concentration remain largely unknown. The global median concentration of dissolved organic carbon in groundwater is low compared to surface waters suggesting significant processing in the subsurface. Yet the processes that remove this dissolved organic carbon (DOC) in groundwater are not fully understood. The purpose of this study was to investigate the different sources and processes influencing DOC in a shallow anoxic coastal aquifer. Uniquely, this study combines liquid chromatography organic carbon detection with inorganic (δ13CDIC) and organic (δ13CDOC) carbon isotope geochemical analyses, to fingerprint the various DOC sources that influence the concentration, carbon isotopic composition and character with distance from surface water sources, depth below surface and groundwater residence time (using 3H) in groundwater. It was found that the average groundwater DOC concentration was five times higher (5 mg L−1) than the global median concentration and it doubled with depth, but the chromatographic character did not change significantly. The anoxic saturated conditions of the aquifer have limited the rate of organic matter processing leading to enhanced preservation and storage of the sources such as peats and palaeosols. All groundwater samples are more aromatic for their molecular weight in comparison to lakes and rivers and surface marine samples. The destabilisation or changes in hydrology, whether by anthropogenic or natural processes could lead to the flux of up to ten times more unreacted organic carbon from this coastal aquifer than compared to deeper inland aquifers.
    Print ISSN: 1812-2108
    Electronic ISSN: 1812-2116
    Topics: Geography , Geosciences
    Published by Copernicus on behalf of European Geosciences Union.
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
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