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Cited by 240

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

Coupled Fe(II)−Fe(III) Electron and Atom Exchange as a Mechanism for Fe Isotope Fractionation during Dissimilatory Iron Oxide Reduction

Crosby, Heidi A., Johnson, Clark M., Roden, Eric E., Beard, Brian L.·2005·Environmental Science & Technology

Abstract

Microbial dissimilatory iron reduction (DIR) is an important pathway for carbon oxidation in anoxic sediments, and iron isotopes may distinguish between iron produced by DIR and other sources of aqueous Fe(II). Previous studies have shown that aqueous Fe(II) produced during the earliest stages of DIR has delta56Fe values that are 0.5-2.0%o lowerthan the initial Fe(III) substrate. The new experiments reported here suggest that this fractionation is controlled by coupled electron and Fe atom exchange between Fe(II) and Fe(III) at iron oxide surfaces. In hematite and goethite reduction experiments with Geobacter sulfurreducens, the 56Fe/54Fe isotopic fractionation between aqueous Fe(II) and the outermost layers of Fe(III) on the oxide surface is approximately -3%o and can be explained by equilibrium Fe isotope partitioning between reactive Fe(II) and Fe(III) pools that coexist during DIR. The results indicate that sorption of Fe(II) to Fe(III) substrates cannot account for production of low-delta56Fe values for aqueous Fe(II) during DIR.

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Metadata

Authors
Crosby, H. A., Johnson, C. M., Roden, E. E., & Beard, B. L.
Venue
Environmental Science & Technology
Published
2005-07-23
Volume
39
Issue
17
Pages
6698-6704
ISSN
  • 0013-936X (ISSN-L)
  • 1520-5851
OpenAlex
W1967199319
Cited by
240
References
6
FWCI
8.70
Type
journal article
Language
en
Open access
closed

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