Isotopic Evidence for Determining the Sources of Dissolved Organic Sulfur in a Forested Catchment

Understanding sulfur (S) biogeochemistry, especially in those watersheds subject to elevated levels of atmospheric S inputs, is needed for determining the factors that contribute to acidification, nutrient losses and the mobilization of toxic solutes (e.g., monomeric aluminum and methylmercury). S i...

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Published inEnvironmental science & technology Vol. 48; no. 19; pp. 11259 - 11267
Main Authors Kang, Phil-Goo, Mitchell, Myron J, Mayer, Bernhard, Campbell, John L
Format Journal Article
LanguageEnglish
Published Washington, DC American Chemical Society 07.10.2014
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Summary:Understanding sulfur (S) biogeochemistry, especially in those watersheds subject to elevated levels of atmospheric S inputs, is needed for determining the factors that contribute to acidification, nutrient losses and the mobilization of toxic solutes (e.g., monomeric aluminum and methylmercury). S is found in a variety of both organic and inorganic forms undergoing a range of biotic and abiotic transformations. In watersheds with decreasing atmospheric S inputs, internal cycling is becoming dominant in affecting whether there is net loss or retention of S. Little attention has been given to the role of dissolved organic S (DOS) in affecting S biogeochemistry. DOS originates from assimilatory and bacterial dissimilatory S reduction (BDSR), the latter of which produces 34S-depleted S. Within groundwater of the Archer Creek Catchment in the Adirondack Mountains (New York) there was reoxidation of reduced S, which was an important source of SO4 2–. DOS in surface waters had a higher variation of δ34S–DOS values (−6.0 to +8.4‰) than inorganic S with δ34S–SO4 2– values ranging from +1.0 to +5.8‰. Inverse correlations between δ34S values of SO4 2– and DOS suggested that BDSR played an important role in producing DOS.
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ISSN:0013-936X
1520-5851
1520-5851
DOI:10.1021/es502563n