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Size, density and composition of cell-mineral aggregates formed during anoxygenic phototrophic Fe(II) oxidation: Impact on modern and ancient environments

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GEOCHIMICA ET COSMOCHIMICA ACTA
卷 74, 期 12, 页码 3476-3493

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.gca.2010.02.036

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Cell-Fe(III) mineral aggregates produced by anoxygenic Fe(II)-oxidizing photoautotrophic microorganisms (photoferrotrophs) may be influential in the modern Fe cycle and were likely an integral part of ancient biogeochemical cycles on early Earth. While studies have focused on the environmental conditions under which modern photoferrotrophs grow and the kinetics, physiology and mechanism of Fe(II) oxidation, no systematic analyses of the physico-chemical characteristics of those aggregates, such as shape, size, density and chemical composition, have as yet been conducted. Herein, experimental results show most aggregates are bulbous or ragged in shape, with an average particle size of 10-40 mu m, and densities that typically range between 2.0 and 2.4 g/cm(3); the cell fraction of the aggregates increased and their density decreased with initial Fe(II) concentration. The mineralogy of the ferric iron phase depended on the composition of the medium: goethite formed in cultures grown by oxidation of dissolved Fe(II) medium in the presence of low phosphate concentrations, while poorly ordered ferrihydrite (or Fe(III) phosphates) formed when amorphous Fe(II) minerals (Fe(II)-phosphates) and high concentrations of phosphate were initially present. Importantly, in all experiments, a fraction of the photoautotrophic cells remained planktonic, demonstrating a constant stoichiometric excess of Fe(III) compared to the autotrophically fixed carbon in the biogenic precipitate. These results not only have an important bearing on nutrient and trace element cycling in the modern water column, but the size, shape and composition of the aggregates can be used to estimate aggregate reactivity during sediment diagenesis over short and geologic time scales. (C) 2010 Elsevier Ltd. All rights reserved.

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