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Isotopic evidence for anoxic pyrite oxidation and stimulation of bacterial sulphate reduction in marine sediments
118
Citations
20
References
2000
Year
EngineeringMicrobial PhysiologyMarine ChemistryAnoxic Pyrite OxidationDesulfurizationOrganic GeochemistryEnvironmental ChemistrySulphate MoleculesBacterial Sulphate ReductionMarine PollutionMicrobial EcologyEnvironmental MicrobiologyMolecular GeochemistryBiogeochemistryChemical OceanographyIncreased Sulphate ConcentrationsEnvironmental EngineeringEarly DiagenesisIsotopic EvidenceGeochemistryMicrobiologyMedicineCoastal GeochemistryMicrobiological Degradation
Pore-water sulphate concentrations show marked increases at depths >50 m at ODP sites 888 and 890/889 from the Cascadia Margin accretionary wedge. In the uppermost 10 m sulphate concentrations decrease with depth and sulphate δ 34 S and δ 18 O increase as sulphate is removed by bacterial sulphate reduction. Isotopic data show that sulphate formed below 50 m results from oxidation of early diagenetic pyrite and that oxygen in the sulphate molecules is derived from pore water. Fe 3+ in the sediment is the probable oxidizing agent. The increased sulphate concentrations stimulate bacterial sulphate reduction at depths of 70–250 m and are thus important in sustaining deep bacterial activity.
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