Environ. Sci. Technol., 41 (8), 2796 -2802, 2007. 10.1021/es0621849 S0013-936X(06)02184-5
Web Release Date: February 28, 2007

Copyright © 2007 American Chemical Society

Oxygen and Chlorine Isotopic Fractionation during Perchlorate Biodegradation: Laboratory Results and Implications for Forensics and Natural Attenuation Studies

Neil C. Sturchio,* John Karl Böhlke, Abelardo D. Beloso, Jr., Sheryl H. Streger, Linnea J. Heraty, and Paul B. Hatzinger

University of Illinois at Chicago, Chicago, Illinois 60607, U.S. Geological Survey, Reston, Virginia 20192, and Shaw Environmental, Inc., Lawrenceville, New Jersey 08648

Received for review September 13, 2006

Revised manuscript received January 16, 2007

Accepted January 29, 2007

Abstract:

Perchlorate is a widespread environmental contaminant having both anthropogenic and natural sources. Stable isotope ratios of O and Cl in a given sample of perchlorate may be used to distinguish its source(s). Isotopic ratios may also be useful for identifying the extent of biodegradation of perchlorate, which is critical for assessing natural attenuation of this contaminant in groundwater. For this approach to be useful, however, the kinetic isotopic fractionations of O and Cl during perchlorate biodegradation must first be determined as a function of environmental variables such as temperature and bacterial species. A laboratory study was performed in which the O and Cl isotope ratios of perchlorate were monitored as a function of degradation by two separate bacterial strains (Azospira suillum JPLRND and Dechlorospirillum sp. FBR2) at both 10 C and 22 C with acetate as the electron donor. Perchlorate was completely reduced by both strains within 280 h at 22 C and 615 h at 10 C. Measured values of isotopic fractionation factors were 18O = -36.6 to -29.0” and 37Cl = -14.5 to -11.5”, and these showed no apparent systematic variation with either temperature or bacterial strain. An experiment using 18O-enriched water (18O = +198”) gave results indistinguishable from those observed in the isotopically normal water (18O = -8.1”) used in the other experiments, indicating negligible isotope exchange between perchlorate and water during biodegradation. The fractionation factor ratio 18O/37Cl was nearly invariant in all experiments at 2.50 ± 0.04. These data indicate that isotope ratio analysis will be useful for documenting perchlorate biodegradation in soils and groundwater. The establishment of a microbial fractionation factor ratio (18O/37Cl) also has significant implications for forensic studies.


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