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Microbial reduction of Fe(III) in the Fithian and Muloorina illites: Contrasting extents and rates of bioreduction

Published online by Cambridge University Press:  01 January 2024

Jennifer L. Seabaugh
Affiliation:
Department of Geology, Miami University, Oxford, OH 45056, USA
Hailiang Dong*
Affiliation:
Department of Geology, Miami University, Oxford, OH 45056, USA
Ravi K. Kukkadapu
Affiliation:
Pacific Northwest National Laboratory, Richland, WA 99352, USA
Dennis D. Eberl
Affiliation:
United States Geological Survey, Boulder, CO 80303, USA
John P. Morton
Affiliation:
Department of Geology, Miami University, Oxford, OH 45056, USA
Jinwook Kim
Affiliation:
Naval Research Laboratory, Seafloor Sciences Branch, Stennis Space Center, MS 39529, USA
*
*E-mail address of corresponding author: [email protected]
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Abstract

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Shewanella putrefaciens CN32 reduces Fe(III) within two illites which have different properties: the Fithian bulk fraction and the <0.2 µm fraction of Muloorina. The Fithian illite contained 4.6% (w/w) total Fe, 81% of which was Fe(III). It was dominated by illite with some jarosite (∼32% of the total Fe(III)) and goethite (11% of the total Fe(III)). The Muloorina illite was pure and contained 9.2% Fe, 93% of which was Fe(III). Illite suspensions were buffered at pH 7 and were inoculated with CN32 cells with lactate as the electron donor. Select treatments included anthraquinone-2,6-disulfonate (AQDS) as an electron shuttle. Bioproduction of Fe(II) was determined by ferrozine analysis. The unreduced and bioreduced solids were characterized by Mössbauer spectroscopy, X-ray diffraction and transmission electron microscopy. The extent of Fe(III) reduction in the bulk Fithian illite was enhanced by the presence of AQDS (73%) with complete reduction of jarosite and goethite and partial reduction of illite. Mössbauer spectroscopy and chemical extraction determined that 21–25% of illite-associated Fe(III) was bioreduced. The extent of bioreduction was less in the absence of AQDS (63%) and only jarosite was completely reduced with partial reduction of goethite and illite. The XRD and TEM data revealed no significant illite dissolution or biogenic minerals, suggesting that illite was reduced in the solid state and biogenic Fe(II) from jarosite and goethite was either released to aqueous solution or adsorbed onto residual solid surfaces. In contrast, only 1% of the structural Fe(III) in Muloorina illite was bioreduced. The difference in the extent and rate of bioreduction between the two illites was probably due to the difference in layer charge and the total structural Fe content between the Fithian illite (0.56 per formula) and Muloorina illite (0.87). There may be other factors contributing to the observed differences, such as expandability, surface area and the arrangements of Fe in the octahedral sheets. The results of this study have important implications for predicting microbe-induced physical and chemical changes of clay minerals in soils and sediments.

Type
Research Article
Copyright
Copyright © 2006, The Clay Minerals Society

References

Dong, H. and Peacor, D.R., (1996) TEM observations of coherent stacking relations in smectite, I/S and illite of shales: evidence for MacEwan crystallites and dominance of 2M 1 polytypism Clays and Clay Minerals 44 257275 10.1346/CCMN.1996.0440211.CrossRefGoogle Scholar
Dong, H. Peacor, D.R. and Freed, R.L., (1997) Phase relations among smectite, R1 I/S and illite American Mineralogist 82 379391 10.2138/am-1997-3-416.CrossRefGoogle Scholar
Dong, H. Fredrickson, J.K. Kennedy, D.W. Zachara, J.M. Kukkadapu, R.K. and Onstott, T.C., (2000) Mineral transformation associated with the microbial reduction of magnetite Chemical Geology 169 299318 10.1016/S0009-2541(00)00210-2.CrossRefGoogle Scholar
Dong, H. Kukkadapu, R.K. Fredrickson, J.K. Zachara, J.M. Kennedy, D.W. and Kostandarithes, H.M., (2003) Microbial reduction of structural Fe(III) in illite and goethite Environmental Science and Technology 37 12681276 10.1021/es020919d.CrossRefGoogle Scholar
Eberl, D.D. Drits, V.A. and Środoń, J., (1998) Deducing growth mechanisms for minerals from the shapes of crystal size distribution American Journal of Science 298 449533 10.2475/ajs.298.6.499.CrossRefGoogle Scholar
Ettler, V. Johan, Z. and Hradil, D., (2003) Natural alteration products of sulphide mattes from primary lead smelting Comptes Rendus Geoscience 335 10131020 10.1016/j.crte.2003.09.006.CrossRefGoogle Scholar
Fanning, D.S. Keramidas, V.Z. El-Desoky, M.A., Dixon, J.B. and Weed, S.B., (1989) Micas Minerals in Soil Environments Madison, Wisconsin Soil Science Society of America 551634.Google Scholar
Fredrickson, J.K. Zachara, J.M. Kennedy, D.W. Dong, H. Onstott, T.C. Hinman, N.W. and Li, S.M., (1998) Biogenic iron mineralization accompanying the dissimilatory reduction of hydrous ferric oxide by a groundwater bacterium Geochimica et Cosmochimica Acta 62 32393257 10.1016/S0016-7037(98)00243-9.CrossRefGoogle Scholar
Fredrickson, J.K. Zachara, J.M. Kukkadapu, R.K. Gorgy, Y.A. Smith, S.C. and Brown, C.F., (2001) Biotransformation of Ni-substituted hydrous ferric oxide by an Fe(III)-reducing bacterium Environmental Science and Technology 35 703712 10.1021/es001500v.CrossRefGoogle ScholarPubMed
Greenwood, N.N. and Gibb, T.C., (1971) Mössbauer Spectroscopy London Chapman & Hall 10.1007/978-94-009-5697-1.CrossRefGoogle Scholar
Hower, J. Eslinger, E.V. Hower, M.H. and Perry, E.A., (1976) Mechanism of burial metamorphism of argillaceous sediments. 1. Mineralogical and chemical evidence Geological Society of America Bulletin 87 725737 10.1130/0016-7606(1976)87<725:MOBMOA>2.0.CO;2.2.0.CO;2>CrossRefGoogle Scholar
Herbert, R.B., (1997) Properties of goethite and jarosite precipitated from acidic groundwater, Dalarna, Sweden Clays and Clay Minerals 45 261273 10.1346/CCMN.1997.0450214.CrossRefGoogle Scholar
Jackson, M.L. Lim, C.H. Zelanzy, L.W. and Klute, A., (1986) Oxides, hydroxides, and aluminosilicates Methods of Soil Analysis, Part 1. Physical and Mineralogical Methods 2nd Madison, Wisconsin American Society of Agronomy-Soil Science Society of America 101150.Google Scholar
Kim, J. Dong, H. Seabaugh, J. and Newell, S.W., (2004) Role of microbes in the smectite-to-illite reaction Science 303 830832 10.1126/science.1093245.CrossRefGoogle ScholarPubMed
Kostka, J.E. Stucki, J.W. Nealson, K.H. and Wu, J., (1996) Reduction of structural Fe(III) in smectite by a pure culture of Shewanella putrefaciens strain MR-1 Clays and Clay Minerals 44 522529 10.1346/CCMN.1996.0440411.CrossRefGoogle Scholar
Kostka, J.E. Haefele, E. Viehweger, R. and Stucki, J.W., (1999) Respiration and dissolution of iron(III)-containing clay minerals by bacteria Environmental Science and Technology 33 31273133 10.1021/es990021x.CrossRefGoogle Scholar
Kostka, J.E. Wu, J. Nealson, K.H. and Stucki, J.W., (1999) The impact of structural Fe(III) reduction by bacteria on the surface chemistry of smectite clay minerals Geochimica et Cosmochimica Acta 63 37053713 10.1016/S0016-7037(99)00199-4.CrossRefGoogle Scholar
Kukkadapu, R.K. Zachara, J.M. Smith, S.C. Fredrickson, J.K. and Liu, C.X., (2001) Dissimilatory bacterial reduction of Al-substituted goethite in subsurface sediments Geochimica Cosmochimica Acta 65 29132924 10.1016/S0016-7037(01)00656-1.CrossRefGoogle Scholar
Kukkadapu, R.K. Zachara, J.M. Fredrickson, J.K. and Kennedy, D.W., (2004) Biotransformation of two-line silica-ferrihydrite by a dissimilatory Fe(III)-reducing bacterium: formation of carbonate green rust in the presence of phosphate Geochimica et Cosmochimica Acta 68 27992814 10.1016/j.gca.2003.12.024.CrossRefGoogle Scholar
Lovely, D.R., (2000) Environmental Microbe-Metal Interactions Washington, D.C ASM Press 10.1128/9781555818098.CrossRefGoogle Scholar
Murad, E. Cashion, J., Murad, E. and Cashion, J., (2004) Iron oxides and oxyhydroxides Mössbauer Spectroscopy of Environmental Materials and their Industrial Applications Boston, USA Springer 159188 10.1007/978-1-4419-9040-2_5.Google Scholar
Nealson, K.H. and Little, B., (1997) Breathing manganese and iron: solid-state respiration Advances in Applied Microbiology 45 213238 10.1016/S0065-2164(08)70264-8.CrossRefGoogle Scholar
Norrish, K. and Pickering, J.G., (1983) Clay minerals Soils, an Australian Viewpoint London Melbourne — CSIRO, Academic Press 281308.Google Scholar
O’Reilly, S.E., Bickmore, B.R. and Furukawa, Y. (2004) Dissolution of microbial reduced nontronite in a flow-through system. Pp. 86 in: 41stAnnual Meeting of the Clay Minerals Society, Program and Abstracts.Google Scholar
Peacor, D.R. and Buseck, P.R., (1992) Diagenesis and low-grade metamorphism of shales and slates Minerals and Reactions at the Atomic Scale: Transmission Electron Microscopy Washington, D.C Mineralogical Society of America 335380 10.1515/9781501509735-013.CrossRefGoogle Scholar
Phillips, E.J.P. and Lovely, D.R., (1987) Determination of Fe(III) and Fe(II) in oxalate extracts of sediments Soil Society of America Journal 51 938941 10.2136/sssaj1987.03615995005100040021x.CrossRefGoogle Scholar
Rancourt, D.G. and Ping, J.Y., (1991) Voigt-based method for arbitrary-shape static hyperfine parameter distributions in Mössbauer spectroscopy Nuclear Instruments and Methods Physics Research 41 891893.Google Scholar
Roden, E.E. and Zachara, J.M., (1996) Microbial reduction of crystalline Fe(III) oxides: Influence of oxide surface area and potential for cell growth Environmental Science and Technology 30 16181628 10.1021/es9506216.CrossRefGoogle Scholar
Stucki, J.W. Komadel, P. and Wilkinson, H.T., (1987) Microbial reduction of structural iron(III) in smectites Soil Science Society of America Journal 51 16631665 10.2136/sssaj1987.03615995005100060047x.CrossRefGoogle Scholar
Taneja, S.P. and Jones, C.H.W., (1984) Mössbauer studies of iron-bearing minerals in coal and coal ash Fuel 63 695701 10.1016/0016-2361(84)90169-8.CrossRefGoogle Scholar
van der Zee, C. Roberts, D.R. Rancourt, D.G. and Slomp, C.P., (2003) Nanogoethite is the dominant reactive oxyhydroxide phase in lake and marine sediments Geology 31 993996 10.1130/G19924.1.CrossRefGoogle Scholar
Zachara, J.M. Fredrickson, J.K. Li, S.M. Kennedy, D.W. Smith, S.C. and Gassman, P.L., (1998) Bacterial reduction of crystalline Fe3+ oxides in single phase suspensions and subsurface materials American Mineralogist 83 14261443 10.2138/am-1998-11-1232.CrossRefGoogle Scholar
Zachara, J.M. Fredrickson, J.K. Smith, S.C. and Gassman, P.L., (2001) Solubilization of Fe(III) oxide-bound trace metals by a dissimilatory Fe(III) reducing bacterium Geochimica et Cosmochimica Acta 65 7593 10.1016/S0016-7037(00)00500-7.CrossRefGoogle Scholar