生物地球化学循环
环境科学
分水岭
溶解有机碳
δ34S
土壤水分
葡萄园
地表水
有机质
环境化学
水文学(农业)
土壤有机质
化学
土壤科学
地质学
地理
环境工程
古生物学
机器学习
考古
有机化学
岩土工程
流体包裹体
石英
计算机科学
作者
Anna L. Hermes,Merritt Logan,Brett A. Poulin,Amy M. McKenna,Todd E. Dawson,Thomas Borch,Eve‐Lyn S. Hinckley
标识
DOI:10.1021/acs.est.3c01347
摘要
Over the past several decades, agricultural sulfur (S) use has dramatically increased. Excess S in the environment can cause several biogeochemical and ecologic consequences, including methylmercury production. This study investigated agriculturally associated changes to organic S─the most dominant form of S within soils─from field-to-watershed scales. Using a novel complementary suite of analytical methods, we combined Fourier transform ion cyclotron resonance mass spectrometry, δ34S-DOS, and S X-ray absorption spectroscopy to characterize dissolved organic S (DOS) in soil porewater and surface water samples from vineyard agriculture (S addition) and forest/grassland areas (no S addition) within the Napa River watershed (California, U.S.). Vineyard soil porewater dissolved organic matter samples had two-fold higher S content compared to forest/grasslands and had unique CHOS2 chemical formulas─the latter also found in tributary and Napa River surface water. The isotopic difference between δ34S-DOS and δ34S–SO42– values provided insights into the likely dominant microbial S processes by land use/land cover (LULC), whereas the S oxidation state did not strongly differ by LULC. The results add to our understanding of the modern S cycle and point to upland agricultural areas as S sources with the potential for rapid S transformations in downgradient environments.
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