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11 - The microbial ecology of land and water contaminated with radioactive waste: towards the development of bioremediation options for the nuclear industry

Published online by Cambridge University Press:  05 June 2012

Andrea Geissler
Affiliation:
Williamson Centre for Molecular Environmental Science, School of Earth, Atmospheric and Environmental Sciences, University of Manchester, United Kingdom
Sonja Selenska-Pobell
Affiliation:
Institute of Radiochemistry, Forschungszentrum Dresden-Rossendorf, Dresden, Germany
Katherine Morris
Affiliation:
Institute of Geological Sciences, School of Earth and Environment, University of Leeds, United Kingdom
Ian T. Burke
Affiliation:
Institute of Geological Sciences, School of Earth and Environment, University of Leeds, United Kingdom
Francis R. Livens
Affiliation:
Centre for Radiochemistry Research, Department of Chemistry, University of Manchester, United Kingdom
Jonathan R. Lloyd
Affiliation:
Centre for Radiochemistry Research, Department of Chemistry, University of Manchester, United Kingdom
Lesley C. Batty
Affiliation:
University of Birmingham
Kevin B. Hallberg
Affiliation:
University of Wales, Bangor
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Summary

Introduction

The release of radionuclides from nuclear and mining sites and their subsequent mobility in the environment is a subject of intense public concern and has promoted much recent research into the environmental fate of radioactive waste (Lloyd & Renshaw 2005b). Naturally occurring radionuclides can input significant quantities of radioactivity into the environment while both natural and artificial/manmade radionuclides have also been released as a consequence of nuclear weapons testing in the 1950s and 1960s, and via accidental release, e.g., from Chernobyl in 1986. The major burden of anthropogenic environmental radioactivity, however, is from the nuclear facilities themselves and includes the continuing controlled discharge of process effluents produced by industrial activities allied to the generation of nuclear power.

Wastes containing radionuclides are produced at the many steps in the nuclear fuel cycle, and vary considerably from low level, high-volume radioactive effluents produced during uranium mining to the intensely radioactive plant, fuel and liquid wastes produced from reactor operation and fuel reprocessing (Lloyd & Renshaw 2005b). The stewardship of these contaminated waste-streams needs a much deeper understanding of the biological and chemical factors controlling the mobility of radionuclides in the environment. Indeed, this is highly relevant on a global stage as anthropogenic radionuclides have been dispersed to the environment both by accident and as part of a controlled/monitored release, e.g., in effluents.

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Publisher: Cambridge University Press
Print publication year: 2010

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References

Akob, D. M., Mills, H. J. and Kostka, J. E. (2007) Metabolically active microbial communities in uranium-contaminated subsurface sediments. FEMS Microbiology Ecology 59, 95–107.CrossRefGoogle ScholarPubMed
Anderson, R. T., Vrionis, H. A., Ortiz-Bernad, I.et al. (2003) Stimulating the in situ activity of Geobacter species to remove uranium from the groundwater of a uranium-contaminated aquifer. Applied and Environmental Microbiology 69, 5884–5891.CrossRefGoogle ScholarPubMed
Beazley, M. J., Martinez, R. J., Sobecky, P. A., Webb, S. M. and Taillefert, M. (2007) Uranium biomineralization as a result of bacterial phosphatase activity: insights from bacterial isolates from a contaminated subsurface. Environmental Science and Technology 41, 5701–5707.CrossRefGoogle ScholarPubMed
Begg, J. D., Burke, I. T. and Morris, K. (2007) The behaviour of technetium during microbial reduction in amended soils from Dounreay, UK. The Science of the Total Environment 373, 297–304.CrossRefGoogle ScholarPubMed
Boukhalfa, H., Icopini, G. A., Reilly, S. D. and Neu, M. P. (2007) Plutonium(IV) reduction by the metal-reducing bacteria Geobacter metallireducens GS15 and Shewanella oneidensis MR1. Applied and Environmental Microbiology 73, 5897–5903.CrossRefGoogle ScholarPubMed
Brodie, E. L., Desantis, T. Z., Joyner, D. C.et al. (2006) Application of a high-density oligonucleotide microarray approach to study bacterial population dynamics during uranium reduction and reoxidation. Applied and Environmental Microbiology 72, 6288–6298.CrossRefGoogle ScholarPubMed
Burke, I. T., Boothman, C., Lloyd, J. R.et al. (2006) Reoxidation behavior of technetium, iron, and sulfur in estuarine sediments. Environmental Science and Technology 40, 3529–3535.CrossRefGoogle ScholarPubMed
Burke, I. T., Boothman, C., Lloyd, J. R., Mortimer, R. J., Livens, F. R. and Morris, K. (2005) Effects of progressive anoxia on the solubility of technetium in sediments. Environmental Science and Technology 39, 4109–4116.CrossRefGoogle ScholarPubMed
Cummings, D. E., Caccavo, F., Spring, S. and Rosenzweig, R. F. (1999) Ferribacterium limneticum, gen. nov., sp. nov., an Fe(III)-reducing micro-organism isolated from mining-impacted freshwater lake sediments. Archives of Microbiology 171, 183–188.CrossRefGoogle Scholar
Finneran, K. T., Housewright, M. E. and Lovley, D. R. (2002) Multiple influences of nitrate on uranium solubility during bioremediation of uranium-contaminated subsurface sediments. Environmental Microbiology 4, 510–516.CrossRefGoogle ScholarPubMed
Finneran, K. T., Johnsen, C. V. and Lovley, D. R. (2003) Rhodoferax ferrireducens sp. nov., a psychrotolerant, facultatively anaerobic bacterium that oxidizes acetate with the reduction of Fe(III). International Journal of Systematic and Evolutionary Microbiology 53, 669–673.CrossRefGoogle Scholar
Fomina, M., Charnock, J. M., Hillier, S., Alavarez, R. and Gadd, G. M. (2007) Fungal transformations of uranium oxides. Environmental Microbiology 9, 1696–1710.CrossRefGoogle ScholarPubMed
Francis, A. J., Dodge, C. J., Lu, F. L., Halada, G. P. and Clayton, C. R. (1994) XPS and XANES studies of uranium reduction by Clostridium sp. Environmental Science and Technology 28, 636–639.CrossRefGoogle ScholarPubMed
Francis, A. J., Gillow, J. B., Dodge, C. J., Harris, R., Beveridge, T. J. and Papenguth, H. W. (2004) Uranium association with halophilic and non-halophilic bacteria and archaea. Radiochimica Acta 92, 481–488.CrossRefGoogle Scholar
Fredrickson, J. K., Zachara, J. M., Balkwill, D. L.et al. (2004) Geomicrobiology of high-level nuclear waste-contaminated vadose sediments at the Hanford Site, Washington State. Applied and Environmental Microbiology 70, 4230–4241.CrossRefGoogle ScholarPubMed
Geissler, A. (2007) Prokaryotic Micro-organisms in Uranium Mining Waste Piles and their Interactions with Uranium and Other Heavy Metals. TU Bergakademi Freiberg. Freiberg, Germany.Google Scholar
Geissler, A. and Selenska-Pobell, S. (2005) Addition of U(VI) to a uranium mining waste sample and resulting changes in the indigenous bacterial community. Geobiology 3, 275–285.CrossRefGoogle Scholar
Holmes, D. E., Finneran, K. T., O'Neil, R. A. and Lovley, D. R. (2002) Enrichment of members of the family Geobacteraceae associated with stimulation of dissimilatory metal reduction in uranium-contaminated aquifer sediments. Applied and Environmental Microbiology 68, 2300–2306.CrossRefGoogle ScholarPubMed
Icopini, G. A., Boukhalfa, H. and Neu, M. P. (2007) Biological reduction of Np(V) and Np(V) citrate by metal-reducing bacteria. Environmental Science and Technology 41, 2764–2769.CrossRefGoogle ScholarPubMed
Istok, J. D., Senko, J. M., Krumholz, L. R.et al. (2004) In situ bioreduction of technetium and uranium in a nitrate-contaminated aquifer. Environmental Science and Technology 38, 468–475.CrossRefGoogle Scholar
John, S. G., Ruggiero, C. E., Hersman, L. E., Tung, C. S. and Neu, M. P. (2001) Siderophore mediated plutonium accumulation by Microbacterium flavescens (JG-9). Environmental Science and Technology 35, 2942–2948.CrossRefGoogle Scholar
Jroundi, F., Merroun, M. L., Arias, J. M., Rossberg, A., Selenska-Pobell, S. and Gonzalez-Munoz, M. T. (2007) Spectroscopic and microscopic characterization of uranium biomineralization in Myxococcus xanthus. Geomicrobiology Journal 24, 441–449.CrossRefGoogle Scholar
Keith-Roach, M. J. and Livens, F. R. (eds.) (2002) Interactions of Micro-organisms with Radionuclides. Elsevier, London.Google Scholar
Law, G. T. W., Geissler, A., Lloyd, J. R.et al. (2008) Manuscript in preparation.
Lloyd, J. R. (2003) Microbial reduction of metals and radionuclides. FEMS Microbiology Reviews 27, 411–425.CrossRefGoogle ScholarPubMed
Lloyd, J. R. and Lovley, D. R. (2001) Microbial detoxification of metals and radionuclides. Current Opinion in Biotechnology 12, 248–253.CrossRefGoogle ScholarPubMed
Lloyd, J. R. and Macaskie, L. E. (1996) A novel PhosphorImager-based technique for monitoring the microbial reduction of technetium. Applied and Environmental Microbiology 62, 578–582.Google ScholarPubMed
Lloyd, J. R. and Macaskie, L. E. (2000) Bioremediation of radioactive metals. In: Environmental Microbe-Metal Interactions (ed. Lovley, D. R.). ASM Press, Washington, DC.Google Scholar
Lloyd, J. R. and Renshaw, J. C. (2005a) Bioremediation of radioactive waste: radionuclide-microbe interactions in laboratory and field-scale studies. Current Opinion in Biotechnology 16, 254–260.CrossRefGoogle ScholarPubMed
Lloyd, J. R. and Renshaw, J. C. (2005b) Microbial transformations of radionuclides: fundamental mechanisms and biogeochemical implications. Metal Ions in Biological Systems 44, 205–240.Google ScholarPubMed
Lloyd, J. R., Chesnes, J., Glasauer, S., Bunker, D. J., Livens, F. R. and Lovley, D. R. (2002) Reduction of actinides and fission products by Fe(III)-reducing bacteria. Geomicrobiology Journal 19, 103–120.CrossRefGoogle Scholar
Lloyd, J. R., Cole, J. A. and Macaskie, L. E. (1997) Reduction and removal of heptavalent Tc from solution by Escherichia coli. Journal of Bacteriology 179, 2014–2021.CrossRefGoogle ScholarPubMed
Lloyd, J. R., Sole, V. A., Praagh, C. V. G. and Lovley, D. R. (2000a) Direct and Fe(II)-mediated reduction of technetium by Fe(III)-reducing bacteria. Applied and Environmental Microbiology 66, 3743–3749.CrossRefGoogle ScholarPubMed
Lloyd, J. R., Yong, P. and Macaskie, L. E. (2000b) Biological reduction and removal of Np(V) by two micro-organisms. Environmental Science and Technology 34, 1297–1301.CrossRefGoogle Scholar
Lovley, D. R. (1993) Dissimilatory metal reduction. Annual Review of Microbiology 47, 263–290.CrossRefGoogle ScholarPubMed
Lovley, D. R. and Phillips, E. J. P. (1992) Reduction of uranium by Desulfovibrio desulfuricans. Applied and Environmental Microbiology 58, 850–856.Google ScholarPubMed
Lovley, D. R., Phillips, E. J. P., Gorby, Y. A. and Landa, E. R. (1991) Microbial reduction of uranium. Nature 350, 413–416.CrossRefGoogle Scholar
Lovley, D. R., Widman, P. K., Woodward, J. C. and Phillips, E. J. P. (1993) Reduction of uranium by cytochrome c3 of Desulfovibrio vulgaris. Applied and Environmental Microbiology 59, 3572–3576.Google ScholarPubMed
Macaskie, L. E., Empson, R. M., Cheetham, A. K., Grey, C. P. and Skarnulis, A. J. (1992) Uranium bioaccumulation by a Citrobacter sp. as a result of enzymatically mediated growth of polycrystalline HUO2PO4. Science 257, 782–784.CrossRefGoogle Scholar
Macaskie, L. E., Jeong, B. C. and Tolley, M. R. (1994) Enzymically accelerated biomineralization of heavy metals – application to the removal of americium and plutonium from aqueous flows. FEMS Microbiology Reviews 14, 351–367.CrossRefGoogle ScholarPubMed
Madden, A. S., Smith, A. C., Balkwill, D. L., Fagan, L. A. and Phelps, T. J. (2007) Microbial uranium immobilization independent of nitrate reduction. Environmental Microbiology 9, 2321–2330.CrossRefGoogle ScholarPubMed
Marshall, M. J., Plymale, A. E., Kennedy, D. W.et al. (2008) Hydrogenase- and outer membrane c-type cytochrome-facilitated reduction of technetium(VII) by Shewanella oneidensis MR-1. Environmental Microbiology 10, 125–136.Google ScholarPubMed
Martinez, R. J., Beazley, M. J., Taillefert, M., Arakaki, A. K., Skolnick, J. and Sobecky, P. A. (2007) Aerobic uranium (VI) bioprecipitation by metal-resistant bacteria isolated from radionuclide- and metal-contaminated subsurface soils. Environmental Microbiology 9, 3122–3133.CrossRefGoogle ScholarPubMed
Martinez, R. J., Wang, Y. L., Raimondo, M. A., Coombs, J. M., Barkay, T. and Sobecky, P. A. (2006) Horizontal gene transfer of P-IB-type ATPases among bacteria isolated from radionuclide- and metal-contaminated subsurface soils. Applied and Environmental Microbiology 72, 3111–3118.CrossRefGoogle ScholarPubMed
McBeth, J. M., Lear, G., Lloyd, J. R., Livens, F. R., Morris, K. and Burke, I. T. (2007) Technetium reduction and reoxidation in aquifer sediments. Geomicrobiology Journal 24, 189–197.CrossRefGoogle Scholar
Merroun, M., Nedelkova, M., Rossberg, A., Hennig, C. and Selenska-Pobell, S. (2006) Interaction mechanisms of bacterial strains isolated from extreme habitats with uranium. Radiochimica Acta 94, 723–729.CrossRefGoogle Scholar
Merroun, M. L., Geipel, G., Nicolai, R., Heise, K. H. and Selenska-Pobell, S. (2003) Complexation of uranium (VI) by three eco-types of Acidithiobacillus ferrooxidans studied using time-resolved laser-induced fluorescence spectroscopy and infrared spectroscopy. Biometals 16, 331–339.CrossRefGoogle ScholarPubMed
Merroun, M. L., Raff, J., Rossberg, A., Hennig, C., Reich, T. and Selenska-Pobell, S. (2005) Complexation of uranium by cells and S-layer sheets of Bacillus sphaericus JG-A12. Applied and Environmental Microbiology 71, 5532–5543.CrossRefGoogle ScholarPubMed
Moon, H. S., Komlos, J. and Jaffe, P. R. (2007) Uranium reoxidation in previously bioreduced sediment by dissolved oxygen and nitrate. Environmental Science and Technology 41, 4587–4592.CrossRefGoogle ScholarPubMed
Morris, K., Livens, F. R., Charnock, J. M.et al. (2008) An X-ray absorption study of the fate of technetium in reduced and reoxidised sediments and mineral phases. Applied Geochemistry 23, 603–617.CrossRefGoogle Scholar
North, N. N., Dollhopf, S. L., Petrie, L., Istok, J. D., Balkwill, D. L. and Kostka, J. E. (2004) Change in bacterial community structure during in situ biostimulation of subsurface sediment cocontaminated with uranium and nitrate. Applied and Environmental Microbiology 70, 4911–4920.CrossRefGoogle ScholarPubMed
Nyman, J. L., Marsh, T. L., Ginder-Vogel, M. A., Gentile, M., Fendorf, S. and Criddle, C. (2006) Heterogeneous response to biostimulation for U(VI) reduction in replicated sediment microcosms. Biodegradation 17, 303–316.CrossRefGoogle ScholarPubMed
Ohnuki, T., Yoshida, T., Ozaki, T.et al. (2005) Interactions of uranium with bacteria and kaolinite clay. Chemical Geology 220, 237–243.CrossRefGoogle Scholar
Ohnuki, T., Yoshida, T., Ozaki, T.et al. (2007) Chemical speciation and association of plutonium with bacteria, kaolinite clay, and their mixture. Environmental Science and Technology 41, 3134–3139.CrossRefGoogle ScholarPubMed
Pedersen, K. (2005) Micro-organisms and their influence on radionuclide migration in igneous rock environments. Journal of Nuclear and Radiochemical Sciences 6, 11–15.CrossRefGoogle Scholar
Renshaw, J. C., Butchins, L. J., Livens, F. R., May, I., Charnock, J. M. and Lloyd, J. R. (2005) Bioreduction of uranium: environmental implications of a pentavalent intermediate. Environmental Science and Technology 39, 5657–5660.CrossRefGoogle ScholarPubMed
Renshaw, J. C., Law, N., Geissler, A., Livens, F. R. and Lloyd, J. R. (2008) Impact of the Fe(III)-reducing bacteria Geobacter sulfurreducens and Shewanella oneidensis on the speciation of plutonium. Short communication. Biogeochemistry submitted.
Renshaw, J. C., Lloyd, J. R. and Livens, F. R. (2007) Microbial interactions with actinides and long-lived fission products. Comptes Rendus Chimie 10, 1067–1077.CrossRefGoogle Scholar
Ruggiero, C. E., Boukhalfa, H., Forsythe, J. H., Lack, J. G., Hersman, L. E. and Neu, M. P. (2005) Actinide and metal toxicity to prospective bioremediation bacteria. Environmental Microbiology 7, 88–97.CrossRefGoogle ScholarPubMed
Selenska-Pobell, S. (2002) Diversity and activity of bacteria in uranium waste piles. In: Interactions of Micro-organisms with Radionuclides (eds. Keith-Roach, M. J. and Livens, F. R.). 225: Elsevier Sciences Ltd, Oxford, UK.Google Scholar
Selenska-Pobell, S., Geissler, A., Merroun, M., Flemming, K., Geipel, G. and Reuther, H. (2008) Biogeochemical changes induced by uranyl nitrate in a uranium mining waste pile. In: Uranium, Mining and Hydrogeology (eds. Merkel, B. J. and Hasche-Berger, A.), pp. 743–752. Springer Verlag, New York.CrossRefGoogle Scholar
Selenska-Pobell, S., Panak, P., Miteva, V., Boudakov, I., Bernhard, G. and Nitsche, H. (1999) Selective accumulation of heavy metals by three indigenous Bacillus strains, B. cereus, B. megaterium and B. sphaericus, from drain waters of a uranium waste pile. FEMS Microbiology Ecology 29, 59–67.CrossRefGoogle Scholar
Senko, J. M., Istok, J. D., Suflita, J. M. and Krumholz, L. R. (2002) In-situ evidence for uranium immobilization and remobilization. Environmental Science and Technology 36, 1491–1496.CrossRefGoogle ScholarPubMed
Shelobolina, E. S., O'Neill, K., Finneran, K. T., Hayes, L. A. and Lovley, D. R. (2003) Potential for in situ bioremediation of a low-pH, high-nitrate uranium-contaminated groundwater. Soil and Sediment Contamination 12, 865–884.CrossRefGoogle Scholar
Shelobolina, E. S., Sullivan, S. A., O'Neill, K. R., Nevin, K. P. and Lovley, D. R. (2004) Isolation, characterization, and U(VI)-reducing potential of a facultatively anaerobic, acid-resistant bacterium from low-pH, nitrate- and U(VI)-contaminated subsurface sediment and description of Salmonella subterranea sp. nov. Applied and Environmental Microbiology 70, 2959–2965.CrossRefGoogle ScholarPubMed
Spain, A. M., Peacock, A. D., Istok, J. D.et al. (2007) Identification and isolation of a Castellaniella species important during biostimulation of an acidic nitrate- and uranium-contaminated aquifer. Applied and Environmental Microbiology 73, 4892–4904.CrossRefGoogle ScholarPubMed
Suzuki, Y. and Banfield, J. (1999) Geomicrobiology of uranium. Reviews in Mineralogy and Geochemistry 38, 393–432.Google Scholar
Suzuki, Y. and Banfield, J. F. (2004) Resistance to, and accumulation of, uranium by bacteria from a uranium-contaminated site. Geomicrobiology Journal 21, 113–121.CrossRefGoogle Scholar
Suzuki, Y., Kelly, S. D., Kemner, K. A. and Banfield, J. F. (2003) Microbial populations stimulated for hexavalent uranium reduction in uranium mine sediment. Applied and Environmental Microbiology 69, 1337–1346.CrossRefGoogle ScholarPubMed
Suzuki, Y., Kelly, S. D., Kemner, K. M. and Banfield, J. F. (2004) Enzymatic U(VI) reduction by Desulfosporosinus species. Radiochimica Acta 92, 11–16.CrossRefGoogle Scholar
Wilkins, M. J., Livens, F. R., Vaughan, D. J., Beadle, I. and Lloyd, J. R. (2007) The influence of microbial redox cycling on radionuclide mobility in the subsurface at a low-level radioactive waste storage site. Geobiology 5, 293–301.CrossRefGoogle Scholar
Wu, Q., Sanford, R. A. and Loffler, F. E. (2006) Uranium(VI) reduction by Anaeromyxobacter dehalogenans strain 2CP-C. Applied and Environmental Microbiology 72, 3608–3614.CrossRefGoogle ScholarPubMed

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