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Applied and Environmental Microbiology, May 1999, p. 2143-2150, Vol. 65, No. 5
Department of Soil
Science,1 Environmental Toxicology
Center,2 and Department of Geology and
Geophysics,3 University of Wisconsin
Received 14 September 1998/Accepted 14 February 1999
This study used phylogenetic probes in hybridization analysis to
(i) determine in situ microbial community structures in regions of a
shallow sand aquifer that were oxygen depleted and fuel contaminated (FC) or aerobic and noncontaminated (NC) and (ii) examine alterations in microbial community structures resulting from exposure to toluene and/or electron acceptor supplementation (nitrate). The latter objective was addressed by using the NC and FC aquifer materials for
anaerobic microcosm studies in which phylogenetic probe analysis was
complemented by microbial activity assays. Domain probe analysis of the
aquifer samples showed that the communities were predominantly Bacteria; Eucarya and Archaea were
not detectable. At the phylum and subclass levels, the FC and NC
aquifer material had similar relative abundance distributions of 43 to
65%
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Molecular Analysis of Microbial Community
Structures in Pristine and Contaminated Aquifers: Field and
Laboratory Microcosm Experiments
Madison,
Madison, Wisconsin, and U.S. Environmental Protection
Agency, National Risk Management Laboratory, Ada,
Oklahoma4
- and
-Proteobacteria (B+G), 31 to 35%
-Proteobacteria (ALF), 15 to 18% sulfate-reducing bacteria, and 5 to 10% high G+C gram positive bacteria. Compared to
that of the NC region, the community structure of the FC material differed mainly in an increased abundance of B+G relative to that of
ALF. The microcosm communities were like those of the field samples in
that they were predominantly Bacteria (83 to 101%) and
lacked detectable Archaea but differed in that a small
fraction (2 to 8%) of Eucarya was detected regardless of
the treatment applied. The latter result was hypothesized to reflect
enrichment of anaerobic protozoa. Addition of nitrate and/or toluene
stimulated microbial activity in the microcosms, but only
supplementation of toluene alone significantly altered community
structures. For the NC material, the dominant subclass shifted from B+G
to ALF, while in the FC microcosms 55 to 65% of the
Bacteria community was no longer identifiable by the phylum
or subclass probes used. The latter result suggested that toluene
exposure fostered the proliferation of phylotype(s) that were otherwise
minor constituents of the FC aquifer community. These studies
demonstrated that alterations in aquifer microbial communities
resulting from specific anthropogenic perturbances can be inferred from
microcosm studies integrating chemical and phylogenetic probe analysis
and in the case of hydrocarbon contamination may facilitate the
identification of organisms important for in situ biodegradation
processes. Further work integrating and coordinating microcosm and
field experiments is needed to explore how differences in scale,
substrate complexity, and other hydrogeological conditions may affect
patterns observed in these systems.
*
Corresponding author. Mailing address: Department of
Soil Science, University of Wisconsin
Madison, Madison, WI 53706-1299. Phone: (608) 262-9018. Fax: (608) 265-2595. E-mail:
wjhickey{at}facstaff.wisc.edu.
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