Chemical Geology · 2013 · 470 citations · 288 references
Natural SciencesEnvironmental SciencesMicrobiologyBiogeochemistryMicrobial MetabolismSoil MicrobiologyBioremediationMicrobial BiogeochemistryMineralizationNutrient MineralizationRedox ChemistryRedox ProcessesAnaerobic Microbial ProcessesBiogeochemical Redox ProcessesBioreductionInorganic Phosphate SolubilizationPhosphatase Enzyme ActivityRedox CyclingSoil Phosphatase ActivityUranium Removal
Microbial metabolism can alter the solubility of priority radionuclides, and biostimulation of anaerobic communities has been explored to remove redox‑sensitive uranium from contaminated groundwater via bioreduction and phosphate biomineralisation. This review examines the mechanisms of uranium bioreduction and phosphate biomineralisation and evaluates their suitability for long‑term precipitation of uranium from groundwater, with a focus on in‑situ trials at DOE field sites. The authors also review redox interactions of other priority radionuclides—including technetium, neptunium, plutonium, americium, iodine, strontium, and caesium—in the context of these bioremediation processes.
Microbial metabolism has the potential to alter the solubility of a broad range of priority radionuclides, including uranium, other actinides and fission products. Of notable interest has been the biostimulation of anaerobic microbial communities to remove redox-sensitive radionuclides such as uranium U(VI) from contaminated groundwaters at nuclear sites. Particularly promising are bioreduction processes, whereby bacteria enzymatically reduce aqueous U(VI) to insoluble U(IV) coupled to oxidation of an organic electron donor; and uranium phosphate biomineralisation, in which bacterial phosphatase activity cleaves organophosphates, liberating inorganic phosphate that precipitates with aqueous U(VI) as uranyl phosphate minerals. Here we review the mechanisms of uranium bioreduction and phosphate biomineralisation and their suitability to facilitate long-term precipitation of uranium from groundwater, with particular focus on in situ trials at the US Department of Energy field sites. Redox interactions of other priority radionuclides (technetium, neptunium, plutonium, americium, iodine, strontium and caesium) are also reviewed.
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