Carbon isotope fractionation by circumneutral iron-oxidizing bacteria

Bacteriogenic iron oxides in natural environments are characterized by an abundance of ferrihydrite precipitates intermixed with bacterial structures that commonly resemble those produced by the lithoautotrophic microorganisms Gallionella ferruginea and Leptohtrix ochracea . These species have been inferred to play a causal role in the formation of bacteriogenic iron oxides, providing a pathway for the reduction of CO 2 and the depletion of 13 C in the organic constituents of bacteriogenic iron oxides. In this study, stable carbon isotope fractionation was determined for bacteriogenic iron oxide samples collected from submarine hydrothermal vents (Axial Volcano, Juan de Fuca Ridge), subterranean (Aspo Hard Rock Laboratory, Sweden) and surficial (Chalk River, Canada) groundwater seeps, and cultures of G . ferruginea . Data were also collected from ferrihydrite samples lacking evidence of bacteria from Bounty Seamount in the vicinity of Pitcairn Island. The mean δ 13 C (‰) of ferrihydrite was determined to be −15.87‰ ± 4.96‰ for the samples from Axial Volcano, −24.97‰ ± 0.43‰ for Aspo, −27.80‰ ± 0.85‰ for Chalk River, −29.3‰ ± 0.2‰ for the microbial culture, and −8.43‰ ± 1.89‰ for the samples from Pitcairn. Samples with the highest concentration of organic carbon also had the lightest δ 13 C in a logarithmic relationship. The consistency of carbon isotope values in relation to the presence of iron-oxidizing bacteria from natural and laboratory samples is interpreted as the ability of these microorganisms to fractionate carbon. The potential of this fractionation to serve as a biosignature holds promise when the resistance of carbon and bacteriogenic ferrihydrite to diagenesis is taken into consideration.

[1]  E. Roden,et al.  Stable Fe isotope fractionations produced by aqueous Fe(II)-hematite surface interactions , 2010 .

[2]  D. Fortin,et al.  Sorption of strontium onto bacteriogenic iron oxides. , 2009, Environmental science & technology.

[3]  J. McManus,et al.  The effect of early diagenesis on the Fe isotope compositions of porewaters and authigenic minerals in continental margin sediments , 2006 .

[4]  E. Roden,et al.  Coupled Fe(II)-Fe(III) electron and atom exchange as a mechanism for Fe isotope fractionation during dissimilatory iron oxide reduction. , 2005, Environmental science & technology.

[5]  Steven D. Scott,et al.  Hydrothermal phase stabilization of 2-line ferrihydrite by bacteria , 2004 .

[6]  F. G. Ferris,et al.  Evidence for microbial-mediated iron oxidation at a neutrophilic groundwater spring , 2004 .

[7]  J. Banfield,et al.  Microbial Polysaccharides Template Assembly of Nanocrystal Fibers , 2004, Science.

[8]  U. Schwertmann,et al.  The Iron Oxides: Structure, Properties, Reactions, Occurrences and Uses , 2003 .

[9]  C. Anderson,et al.  In situ growth of Gallionella biofilms and partitioning of lanthanides and actinides between biological material and ferric oxyhydroxides , 2003 .

[10]  F. G. Ferris,et al.  Ultrastructure and potential sub-seafloor evidence of bacteriogenic iron oxides from Axial Volcano, Juan de Fuca Ridge, north-east Pacific Ocean. , 2003, FEMS microbiology ecology.

[11]  C. Moyer,et al.  Neutrophilic Fe-Oxidizing Bacteria Are Abundant at the Loihi Seamount Hydrothermal Vents and Play a Major Role in Fe Oxide Deposition , 2002, Applied and Environmental Microbiology.

[12]  D. Gröcke The carbon isotope composition of ancient CO2 based on higher-plant organic matter. , 2002, Philosophical transactions. Series A, Mathematical, physical, and engineering sciences.

[13]  C. W. Childs,et al.  Demonstration of significant abiotic iron isotope fractionation in nature , 2001 .

[14]  J. Banfield,et al.  Aggregation-based crystal growth and microstructure development in natural iron oxyhydroxide biomineralization products. , 2000, Science.

[15]  F. G. Ferris,et al.  Retention of strontium, cesium, lead and uranium by bacterial iron oxides from a subterranean environment , 2000 .

[16]  D. Fortin,et al.  Formation of Fe-silicates and Fe-oxides on bacterial surfaces in samples collected near hydrothermal vents on the Southern Explorer Ridge in the northeast Pacific Ocean , 1998 .

[17]  G. Massoth,et al.  Biological colonization of new hydrothermal vents following an eruption on Juan de Fuca Ridge , 1997 .

[18]  T. Beveridge,et al.  Modern freshwater microbialites from Kelly Lake, British Columbia, Canada , 1997 .

[19]  K. Pedersen,et al.  Autotrophic and mixotrophic growth of Gallionella ferruginea , 1991 .

[20]  K. Pedersen,et al.  Culture parameters regulating stalk formation and growth rate of Gallionella ferruginea , 1990 .

[21]  N. Holm Carbon isotope distribution in organic matter and siderite of a modern metalliferous hydrothermal sediment and possible implications for gold associated with banded iron formation , 1988 .

[22]  Y. Fouquet,et al.  Filamentous iron-silica deposits from modern and ancient hydrothermal sites , 1988 .

[23]  J. Alt Hydrothermal oxide and nontronite deposits on seamounts in the eastern Pacific , 1988 .

[24]  C. Yapp,et al.  Carbon in natural goethites , 1986 .

[25]  Walter E. Dean,et al.  Determination of carbonate and organic matter in calcareous sediments and sedimentary rocks by loss on ignition; comparison with other methods , 1974 .

[26]  R. Wolfe,et al.  A SELECTIVE ENRICHMENT METHOD FOR GALLIONELLA FERRUGINEA , 1957, Journal of bacteriology.

[27]  B. Beard,et al.  Fe isotopes: An emerging technique for understanding modern and ancient biogeochemical cycles , 2006 .

[28]  D. Garbe‐Schönberg,et al.  Hydrothermal Iron and Manganese Crusts from the Pitcairn Hotspot Region , 2004 .

[29]  D. Emerson Microbial Oxidation of Fe(II) and Mn(II) at Circumneutral pH , 2000 .