The abundance of aerobic microorganisms, the influence of sediment properties and groundwater geochemistry on microbial processes, and
the community structure of bacteria were investigated in sediments of
a Gulf Coast aquifer. Five boreholes were drilled into the sands,
silts, clays, and lignite of the Eocene Yegua formation in
east-central Texas, and monitoring wells were installed in all
water-bearing sands. Numbers of microorganisms ranged from 10^6 to
10^8 cells per gram dry weight (gdw-1), and viable counts ranged from
0 to 10^6 cells gdw-1. Numbers of S- and Fe-oxidizing bacteria
decreased with depth and ranged from 0 to 10^2 cells gdw–1. Low pH
(3.8) and high sulfate (28 mM) and Fe2+ (0.3 mM) contents argue for
pyrite oxidation in shallow sediments. S- and Fe-oxidizing bacteria
were readily detected in these sediments and likely play a role in
pyrite oxidation. In consistent fashion, there was a relative paucity
of pyrite in shallow sediments and a low 34S/32SSulfate ratio (0.2‰),
reflecting contributions from 34S-depleted sulfides, in shallow
regions. This pyrite oxidation potentially supplies sulfate to the
deeper aquifers.
PCR amplification of 16S rDNA genes from sediment and water samples,
using primer sets specific for the domain Bacteria and others specific
for organisms of the genus Thiobacillus, yielded amplification that
corresponded well with sediment geochemistry. Amplified DNA fragments
of the V3 region of 16s rDNA were resolved by denaturing gradient gel
electrophoresis (DGGE), and the resulting profiles were reproducible
and specific for communities from different depths. Bacterial
diversity estimated from the number and intensity of specific
fragments in DGGE profiles decreased with depth. DNA amplified with
primers specific for T. ferrooxidans and T. thiooxidans showed the
presence of T. ferrooxidans to be most abundant above the
oxidizing-to-reducing transition zone. Organisms isolated from the
Yegua formation were phylogenetically most closely related to the
species T. ferrooxidans and T. thiooxidans based on comparative
molecular sequence (16s rDNA) analysis. Overall, sulfur cycling in
shallow sediments and the transport of sulfate represents an important
mechanism for commensal interaction among subsurface microorganisms by
providing electron donors for chemoautotrophic bacteria and electron acceptors for
heterotrophic bacteria.