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Mitigation of Acid Mine Drainage and Other Contamination
in the Prince William Forest National Park in Northern
Virginia
Michael Komelaslky, Douglas Mose and George Mushrush,
Chemistry Department, George Mason University, Fairfax, VA
22030, Tel/Fax:
703-273-2282
Prolonged use of northern Virginia forests produced
contamination problems in an area that is now a new
National Park. Pyrite mining of shallow hydrothermal
ore deposits for about 50 years, which ended about 50
years ago, produced mine tailings that still produce
acidic and metal-enriched groundwater to the local streams
and wetlands. Military training facilities contributed
vehicle fuels lubricants, and some metal contamination.
Recently, relatively dense housing developments contribute
road runoff. Measurements of stream waters and stream
sediment throughout the park reveal that mitigation
efforts have significantly reduced or eliminated most of
the contamination, though the acid mine drainage still is
present, in spite of extensive remediation efforts.
Monitoring
Changes in Microbial Ecology during Sulfate Amendment of a
BTEX-Contaminated Aquifer using Bio-Sep Traps
Kerry
Sublette, University of Tulsa, Tulsa, OK
Aaron Peacock, University of Tennessee, Knoxville, TN
Ravi Kolhatkar, Group Environmental Management Co. (BP),
La Palma, CA
Dennis Beckman, Group Environmental Management Co. (BP),
Tulsa, OK
David Cook, GeoEngineers, Seattle, WA
David White, University of Tennessee, Knoxville, TN
Thomas Mathew, University of Tulsa, Tulsa, OK
Chintan Mehta, University of Tulsa, Tulsa, OK
Greg Davis, Microbial Insights, Inc., Rockford, TN
A gasoline-contaminated aquifer in Washington state has been
under remediation since 1999 using soil-vapor extraction
and catalytic oxidation following a period of free product
removal. By late 2002 the highest benzene concentrations in the plume
were 0.8-4 mg/L. A
field trial is currently underway to enhance natural
attenuation of hydrocarbons at the site by amending the
aquifer with sulfate which is introduced into the aquifer
using an infiltration trench in 1000-gal batches at a
concentration of 500 mg/L.
Bio-Sep® consists of 3-4 mm diameter spherical
beads engineered from a composite of 25% aramid polymer (Nomex)
and 75% powdered activated carbon (PAC). The bulk density
is about 0.16 g/cm3 with a porosity of 74%.
Beads are surrounded by an ultrafiltration-like
membrane with pores of 1-10 microns.
Bio-Sep® beads have been shown to be
very effective in collecting biofilms which are believed
to be more indicative of in
situ microbial ecology than planktonic organisms from
groundwater samples.
Bio-Sep® beads may also be “baited”
with potential remediation amendments during fabrication
or loaded onto PAC post fabrication
Prior to initiation of the field trial five groundwater
monitoring wells (one upgradient, three plume, and one
fringe) were investigated to predict the effect of the
sulfate amendment on subsurface microbial ecology by
incubating two types of Bio-Sep® traps in each
well. In
each well one trap contained non-baited Bio-Sep®
beads. The
second trap contained both non-baited beads and beads in
which Na2SO4 had been incorporated
during fabrication. The
baited beads provided a source of slow-release sulfate in
the trap to mimic the effect of sulfate amendment of the
aquifer. After
30 days of incubation the trap biofilms were analyzed
using phospholipid fatty acid (PLFA) analysis and analysis
of PCR-amplified 16S rDNA.
Biofilms from the sulfate-baited traps and the non-baited
traps were shown to have distinctly different community
structures. Sulfate-baited
traps were more likely to contain lipid anaerobic
biomarkers, biomarkers for sulfate-reducing bacteria, and
specifically identified anaerobes like Geobacter
sp. The
aquifer is currently being monitored using non-baited
Bio-Sep® traps to determine whether the
predicted shifts in the subsurface microbial ecology are
observed as the sulfate amendment is introduced.
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