Sedimentology · 1996 · 61 citations · 34 references
Natural SciencesEarth SciencesGeologyGeochemistryMarine GeologyPetrologyDepositional Environment AnalysisDepositional EnvironmentsSedimentary EnvironmentsSedimentary PetrologySedimentary RocksSource Rock GeologyCarbon DioxideDepositional Environment InferenceDepositional Environment Of Source RocksDepositional Environment ReconstructionIsotopic Composition AnalysisIsotopic FractionationMethane OxidationSedimentary Diagenesis
ABSTRACT Early concretionary and non‐concretionary siderites are common in subsurface Triassic sandstones and mudrocks of the Rewan Group, southern Bowen Basin. A detailed petrological and stable isotopic study was carried out on these siderites in order to provide information on the depositional environment of the host rocks. The siderites are extremely pure, containing 85–97 mol% FeCO 3 , and are commonly enriched in manganese. δ 13 C (PDB) values are highly variable, ranging from ‐ 18·4 to +2·9‰, whereas δ 18 O (PDB) values are very consistent, ranging from ‐ 14·0 to ‐ 10·2‰ (mean= ‐ 11·9 ± 1·0‰). The elemental and oxygen isotopic composition of the siderites indicates that only meteoric porewaters were involved in siderite formation, implying that host rocks accumulated in totally non‐marine environments. The carbon isotopic composition of the siderites is interpreted to reflect mixing of bicarbonate/carbon dioxide generated by methane oxidation and methanogenesis. Very low δ 13 C values demonstrate that, contrary to current views, highly 13 C‐depleted siderite can be produced at shallow burial depths in anoxic non‐marine sediments.
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Reduction of Fe(III) in sediments by sulphate-reducing bacteria
Max Coleman, David B. Hedrick, Derek R. Lovley et al. · Nature · 1993 · 482 citations