Anaerobic sulfide oxidation and stable isotope fractionation associated with 
bacterial sulfur disproportionation in the presence of MnO2

Böttcher, Michael E.; Thamdrup, Bo

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Anaerobic sulfide oxidation and stable isotope fractionation associated with bacterial sulfur disproportionation in the presence of MnO2

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Böttcher, Michael E.
Department of Biogeochemistry, Max Planck Institute for Marine Microbiology, Max Planck Society;

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Böttcher, M. E., & Thamdrup, B. (2001). Anaerobic sulfide oxidation and stable isotope fractionation associated with bacterial sulfur disproportionation in the presence of MnO2. Geochimica et Cosmochimica Acta, 65(10), 1573-1581.

Cite as: https://hdl.handle.net/21.11116/0000-0003-FCC1-7

Abstract

The sulfur and oxygen isotope effects associated with anaerobic bacterial disproportionation of elemental sulfur by a pure culture (Desulfocapsa thiozymogenes) and an enrichment culture were investigated experimentally in the presence of synthetic Mn(IV)oxides. During bacterial disproportionation, 34S/32S were fractionated in dissolved sulfate compared to elemental sulfur by −0.6 to +2.0‰ (D. thiozymogenes) and −0.2 to +1.1‰ (enrichment culture) at cellular sulfur disproportionation rates of 10−16 mol S°/cell/h and 10−17 mol S°/cell/h, respectively. The measured sulfur isotope effects are much smaller than those observed previously for the same cultures in the presence of Fe(III) and Fe(II) compounds, indicating that microbial isotope fractionation was superimposed by the chemical re-oxidation of hydrogen sulfide by MnO2 to sulfate. Significant re-oxidation of H2S to sulfate was additionally confirmed by the oxygen isotopic composition of sulfate, which was enriched in 18O compared to water by +8 to +12‰. These new experimental results imply that the overall influence of bacterial disproportionation on stable isotope partitioning in natural surface sediments depends on the proportion and relative recycling rates of reactive Fe(III) to Mn(IV)(oxyhydr)oxides.