4.7 Article

Identifying sources and cycling of phosphorus in the sediment of a shallow freshwater lake in China using phosphate oxygen isotopes

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 676, Issue -, Pages 823-833

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.scitotenv.2019.04.322

Keywords

Sources and cycling; Phosphorus; Sediment; Fe-57-Mossbauer spectroscopy; Phosphate oxygen isotopes

Funding

  1. National Science Foundation [1738770, 1757353]
  2. National Natural Science Foundation of China [41503099]
  3. Natural Science Foundation of Jiangsu Province [BK20150902, BK20170948]
  4. China Scholarship Council (CSC)
  5. Office Of The Director
  6. Office of Integrative Activities [1738770] Funding Source: National Science Foundation
  7. Office Of The Director
  8. Office of Integrative Activities [1757353] Funding Source: National Science Foundation

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Biotic and abiotic pathways for the transformation of phosphorus (P) in the sediment of Taihu Lake, a eutrophic shallow freshwater lake in southeastern China, were studied using the oxygen isotope ratios of phosphate (delta O-18(P)) along with sediment chemistry, X-ray diffraction, and Fe-57-Mossbauer spectroscopic methods. The results showed that delta O-18(P) values of sediment P pools significantly deviated from equilibrium and thus allowed distinguishing potential P sources or pathways of transformation. Isotope values of authigenic P being lighter than equilibrium suggests the re-mineralization of organic matter and subsequent precipitation of apatite as the major pathway of formation of authigenic P. The delta O-18(P) values of the Al-bound P pool (18.9-23.5 parts per thousand) and ferric Fe-bound P (16.79-19.86 parts per thousand) could indicate potential terrestrial sources, but the latter being closer to equilibrium values implies partial overprinting of potential source signature, most likely due to reductive dissolution and release of P and followed by partial biological cycling before re-sorption/re-precipitation with newly formed ferric Fe minerals. Oxic/anoxic oscillation and dissolution/re-precipitation reactions and expected isotope excursion are corroborated by sediment chemistry and Mossbauer spectroscopic results. These findings provide improved insights for better understanding the origin and biogeochemical cycling of P associated with eutrophication in shallow freshwater lakes. (C) 2019 Elsevier B.V. All rights reserved.

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