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278 - Microbial Subsurface Repopulation Following In Situ STAR<br />

Remediation<br />

Gavin Overbeeke & Jason Gerhard<br />

Department of Civil and Environmental Engineering – University of Western Ontario,<br />

London, Ontario, Canada<br />

Elizabeth Edwards<br />

Department of Chemical Engineering and Applied Chemistry – University of Toronto,<br />

Toronto, Ontario, Canada<br />

Gavin Grant<br />

Savron, Guelph, Ontario, Canada<br />

STAR (Self-sustaining Treatment for Active Remediation) is an emerging remediation<br />

technology that employs a self-sustaining smouldering reaction to destroy nonaqueous<br />

phase liquids (NAPLs) in the subsurface. The reaction is a slow, controlled, flameless exothermic<br />

oxidation reaction that proceeds strictly through NAPL-contaminated soil. The<br />

reaction front travels at rates of 0.5 to 5 m per day and subjects the soil to temperatures<br />

between 400°C and 1000°C. As a result, not only does STAR cause in situ destruction of<br />

NAPL, but it thoroughly dries and likely sterilizes the soil through which it passes. The<br />

objective of this work is to monitor the re-saturation of the soil over time and quantify<br />

the microbial repopulation of the treated source zone. STAR is currently being applied as<br />

a full scale, in situ remedy for coal tar beneath a former creosol manufacturing facility in<br />

New Jersey, USA. STAR is being applied at two depths where significant coal tar contamination<br />

is observed: a shallow fill unit and a deeper fine sand alluvial aquifer, both beneath<br />

the water table. This project includes analysis of soil cores and groundwater samples taken<br />

from both depths immediately after STAR treatment and at regular intervals afterwards,<br />

allowing time for groundwater to reinfiltrate and for microbial populations to reestablish.<br />

Samples were also taken from outside the treatment zones to provide background data.<br />

Both soil and groundwater samples were analyzed for total number of microorganisms<br />

and microbial diversity using Pyrotag analysis. Pyrotag analysis subjects DNA within a soil<br />

sample to quantitative Polymerase Chain Reaction (qPCR), which is used to estimate the<br />

abundance of microorganisms, as well as Amplicon sequencing of 16srRNA genes, which<br />

provides an estimation of microbial composition and diversity. To inform the field research<br />

program, an initial bench top laboratory study using site soil and natural groundwater<br />

is exploring the rate at which STAR-treated soil is repopulated with naturally occurring<br />

microorganisms. The expectation of this research program is to provide insight into the<br />

changes in microbial abundance and diversity as the subsurface transitions from contaminated<br />

to remediated and then repopulated soil. The rate at which the microbial abundance<br />

changes, as well as the variations seen in microbial diversity will be a key factor in determining<br />

the rate at which the subsurface improves towards its natural soil function.<br />

196 - Importance of Groundwater Flow Direction Match in<br />

Groundwater Flow Model Calibration<br />

Hongze Gao & Steve Harris<br />

Conestoga Rovers & Associates, a GHD Company, Waterloo, Ontario, Canada<br />

166 IAH-CNC 2015 WATERLOO CONFERENCE

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