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The oxidation of sulfide, generated by bacterial sulfate reduction, is a key process in the biogeochemistry of marine sediments, yet the pathways and oxidants are poorly known. By the use of (35)S-tracer studies of the S cycle in marine and freshwater sediments, a novel shunt function of thiosulfate (S(2)O(3)(2-)) was identified. The S(2)O(3)(2-) constituted 68 to 78 percent of the immediate HS(-)-oxidation products and was concurrently (i) reduced back to HS(-), (ii) oxidized to SO(4)(2-), and (iii) disproportionated to HS(-) + SO(4)(2-). The small thiosulfate pool is thus involved in a dynamic HS(-) - S(2)O(3)(2-) cycle in anoxic sediments. The disproportionation of thiosulfate may help account for the large difference in isotopic composition ((34)S/(32)S) of sulfate and sulfides in sediments and sedimentary rocks.
Bo Barker Jørgensen (Fri,) studied this question.
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