Bacterial Oxidation of Methyl Bromide in Mono Lake, California

Tracy L. Connell, Samantha B. Joye, Laurence G. Miller, and Ronald S. Oremland*
U.S. Geological Survey, 345 Middlefield Park, Menlo Park, California 94025, and Texas A&M University, College Station, Texas 77843
Environ. Sci. Technol., 1997, 31 (5), pp 1489–1495
DOI: 10.1021/es960732k
Publication Date (Web): April 29, 1997
Copyright © 1997 American Chemical Society

 U.S. Geological Survey.

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 Texas A&M University.

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*

 Corresponding author:  telephone:  (415) 329-4482; fax:  (415) 329-4463; e-mail:  roremlan@usgs.gov.

Abstract

The oxidation of methyl bromide (MeBr) in the water column of Mono Lake, CA, was studied by measuring the formation of H14CO3 from [14C]MeBr. Potential oxidation was detected throughout the water column, with highest rates occurring in the epilimnion (5−12 m depth). The oxidation of MeBr was eliminated by filter-sterilization, thereby demonstrating the involvement of bacteria. Vertical profiles of MeBr activity differed from those obtained for nitrification and methane oxidation, indicating that MeBr oxidation is not simply a co-oxidation process by either nitrifiers or methanotrophs. Furthermore, specific inhibitors of methane oxidation and/or nitrification (e.g., methyl fluoride, acetylene, allyl sulfide) had no effect upon the rate of MeBr oxidation in live samples. Of a variety of potential electron donors added to Mono Lake water, only trimethylamine resulted in the stimulation of MeBr oxidation. Cumulatively, these results suggest that the oxidation of MeBr in Mono Lake waters is attributable to trimethylamine-degrading methylotrophs. Neither methyl chloride nor methanol inhibited the oxidation of [14C]MeBr in live samples, indicating that these bacteria directly oxidized MeBr rather than the products of MeBr nucleophilic substitution reactions.

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History

  • Published In Issue April 29, 1997
  • Received for review August 26, 1996
    Revised manuscript received December 5, 1996
    Accepted December 16, 1996

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