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Updated: Jan 2, 2026

Preparation of Authigenic Pyrite from Methane-bearing Sediments for In Situ Sulfur Isotope Analysis Using SIMS
Published on: August 31, 2017
Photochemical Alteration of Dissolved Organic Sulfur from Sulfidic Porewater
Gonzalo V Gomez-Saez1, Anika M Pohlabeln1, Aron Stubbins2
1Research Group for Marine Geochemistry (ICBM - MPI Bridging Group), Institute for Chemistry and Biology of the Marine Environment, Carl von Ossietzky University of Oldenburg , D-26111 Oldenburg, Germany.
Abstract:
Sulfidic sediments are a source of dissolved organic sulfur (DOS) to the ocean but the fate of sedimentary DOS in the oxic, sunlit water column is unknown. We hypothesized that photodegradation after discharge from the dark sedimentary environment results in DOS molecular transformation and decomposition. To test this hypothesis, sulfidic porewater from a saltmarsh was exposed to potential abiotic transformations of dissolved organic matter (DOM) in the water column. We quantitatively investigated DOM transformations via elemental analysis and molecularly via ultrahigh-resolution mass spectrometry. Our study indicated that photoreactivity is dependent on DOM elemental composition as DOS molecular formulas were more photolabile than those without sulfur. Prior to solar irradiation, of the 6451 identified molecular formulas in sulfidic porewater, 39% contained sulfur. After 29 days of irradiation, the DOS concentration was depleted from 13 to 1 μM, together with a 9% decrease in the number of DOS molecular formulas. Comparing porewater and oceanic DOS molecular formulas, solar irradiation increased the similarity due to the removal of photolabile DOS formulas not present in the ocean. In conclusion, DOS from sulfidic sediments is preferentially photolabile and solar irradiation can be a potential mechanism controlling the stability and fate of porewater DOS.
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