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Ferrous iron (FeII) oxidation is an important pathway for generating reactive FeIII phases in soils, which can affect organic carbon (OC) persistence/decomposition. We explored how pO₂ concentration influences FeII oxidation rates and FeIII mineral composition, and how this impacts the subsequent FeIII reduction and anaerobic OC mineralization following a transition from oxic to anoxic conditions. We conducted batch soil slurry experiments within a humid tropical forest soil amended with isotopically labeled ⁵⁷FeII. The slurries were oxidized with either 21% or 1% pO₂ for 9 days and then incubated for 20 days under anoxic conditions. Exposure to 21% pO₂ led to faster FeII oxidation rates and greater partitioning of the amended ⁵⁷Fe into low-crystallinity FeIII-(oxyhydr)oxides (based on Mössbauer analysis) than exposure to 1% pO₂. During the subsequent anoxic period, low-crystallinity FeIII-(oxyhydr)oxides were preferentially reduced relative to more crystalline forms with higher net rates of anoxic FeII and CO₂ production-which were well correlated-following exposure to 21% pO₂ than to 1% pO₂. This study illustrates that in redox-dynamic systems, the magnitude of O₂ fluctuations can influence the coupled iron and organic carbon cycling in soils and more broadly, that reaction rates during periods of anoxia depend on the characteristics of prior oxidation events.
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Chen et al. (2018) studied this question.
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