1991
DOI: 10.1080/09593339109385029
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Bioremediation of a creosote contaminated site

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Cited by 53 publications
(17 citation statements)
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“…The principal sources of PAHs in soils along highways and roads are vehicular exhausts and emissions from wearing of tires and asphalt. PAHs may also be released to soils at concentrations above background and landfill sites (Black et al 1989) and industrial sites, including creosote production (Ellis et al 1991), wood-preserving (Mueller et al 1991;Weissenfels et al 1990), and coking plants (Weissenfels et al 1990;Werner et al 1988). Soils at the sites of former manufactured gas plants are also heavily contaminated with PAHs (Bewley et al 1989;Tumey and Goerlitz 1990).…”
Section: Soilmentioning
confidence: 99%
“…The principal sources of PAHs in soils along highways and roads are vehicular exhausts and emissions from wearing of tires and asphalt. PAHs may also be released to soils at concentrations above background and landfill sites (Black et al 1989) and industrial sites, including creosote production (Ellis et al 1991), wood-preserving (Mueller et al 1991;Weissenfels et al 1990), and coking plants (Weissenfels et al 1990;Werner et al 1988). Soils at the sites of former manufactured gas plants are also heavily contaminated with PAHs (Bewley et al 1989;Tumey and Goerlitz 1990).…”
Section: Soilmentioning
confidence: 99%
“…PAHs are widely distributed in soils and sediments, groundwater and the atmosphere. They have been detected in marine sediments such as San Diego Bay, California8, 9 and the Central Pacific ocean,10 intertidal sediments,11 gas works site soils,12, 13 sewage sludge‐contaminated soils,14 aquifers and groundwater and in atmospheric deposits such as vehicle exhaust fumes 4…”
Section: Introductionmentioning
confidence: 99%
“…Alternatively, the treatment scheme of multiple additions of creosote simulated a situation in which PAHs are leached from a point source such as contaminated sediments, leading to a chronic exposure [31]. In both treatment regimes, PAH concentrations in the water were diminished shortly after treatment was complete, presumably by partitioning to the sediment, pool liners, and biotic components of the microcosm and by volatilization to the air phase for the lower-molecular-weight PAHs [40] and biodegradation by bacteria [28,41]. However, in the microcosms treated using multiple additions of creosote, aqueous PAHs remained at higher concentrations over time.…”
Section: Discussionmentioning
confidence: 99%