Stable Carbon Isotope Evidence for Intrinsic Bioremediation of Tetrachloroethene and Trichloroethene at Area 6, Dover Air Force Base
Area 6 at Dover Air Force Base (Dover, DE) has been the location of an in-depth study by the RTDF (Remediation Technologies Development Forum Bioremediation of Chlorinated Solvents Action Team) to evaluate the effectiveness of natural attenuation of chlorinated ethene contamination in groundwater. C...
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Veröffentlicht in: | Environmental science & technology 2001-01, Vol.35 (2), p.261-269 |
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creator | Sherwood Lollar, B Slater, G. F Sleep, B Witt, M Klecka, G. M Harkness, M Spivack, J |
description | Area 6 at Dover Air Force Base (Dover, DE) has been the location of an in-depth study by the RTDF (Remediation Technologies Development Forum Bioremediation of Chlorinated Solvents Action Team) to evaluate the effectiveness of natural attenuation of chlorinated ethene contamination in groundwater. Compound-specific stable carbon isotope measurements for dissolved PCE and TCE in wells distributed throughout the anaerobic portion of the plume confirm that stable carbon isotope values are isotopically enriched in 13C consistent with the effects of intrinsic biodegradation. During anaerobic microbial reductive dechlorination of chlorinated hydrocarbons, the light (12C) versus heavy isotope (13C) bonds are preferentially degraded, resulting in isotopic enrichment of the residual contaminant in 13C. To our knowledge, this study is the first to provide definitive evidence for reductive dechlorination of chlorinated hydrocarbons at a field site based on the δ13C values of the primary contaminants spilled at the site, PCE and TCE. For TCE, downgradient wells show δ13C values as enriched as −18.0‰ as compared to δ13C values for TCE in the source zone of −25.0 to −26.0‰. The most enriched δ13C value on the site was observed at well 236, which also contains the highest concentrations of cis-DCE, VC, and ethene, the daughter products of reductive dechlorination. Stable carbon isotope signatures are used to quantify the relative extent of biodegradation between zones of the contaminant plume. On the basis of this approach, it is estimated that TCE in downgradient well 236 is more than 40% biodegraded relative to TCE in the proposed source area. |
doi_str_mv | 10.1021/es001227x |
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F ; Sleep, B ; Witt, M ; Klecka, G. M ; Harkness, M ; Spivack, J</creator><creatorcontrib>Sherwood Lollar, B ; Slater, G. F ; Sleep, B ; Witt, M ; Klecka, G. M ; Harkness, M ; Spivack, J</creatorcontrib><description>Area 6 at Dover Air Force Base (Dover, DE) has been the location of an in-depth study by the RTDF (Remediation Technologies Development Forum Bioremediation of Chlorinated Solvents Action Team) to evaluate the effectiveness of natural attenuation of chlorinated ethene contamination in groundwater. Compound-specific stable carbon isotope measurements for dissolved PCE and TCE in wells distributed throughout the anaerobic portion of the plume confirm that stable carbon isotope values are isotopically enriched in 13C consistent with the effects of intrinsic biodegradation. During anaerobic microbial reductive dechlorination of chlorinated hydrocarbons, the light (12C) versus heavy isotope (13C) bonds are preferentially degraded, resulting in isotopic enrichment of the residual contaminant in 13C. To our knowledge, this study is the first to provide definitive evidence for reductive dechlorination of chlorinated hydrocarbons at a field site based on the δ13C values of the primary contaminants spilled at the site, PCE and TCE. For TCE, downgradient wells show δ13C values as enriched as −18.0‰ as compared to δ13C values for TCE in the source zone of −25.0 to −26.0‰. The most enriched δ13C value on the site was observed at well 236, which also contains the highest concentrations of cis-DCE, VC, and ethene, the daughter products of reductive dechlorination. Stable carbon isotope signatures are used to quantify the relative extent of biodegradation between zones of the contaminant plume. On the basis of this approach, it is estimated that TCE in downgradient well 236 is more than 40% biodegraded relative to TCE in the proposed source area.</description><identifier>ISSN: 0013-936X</identifier><identifier>EISSN: 1520-5851</identifier><identifier>DOI: 10.1021/es001227x</identifier><identifier>PMID: 11347596</identifier><identifier>CODEN: ESTHAG</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Biodegradation ; Biodegradation, Environmental ; Bioremediation ; Carbon ; Carbon Isotopes - analysis ; Chlorine compounds ; Contamination ; Delaware ; Earth sciences ; Earth, ocean, space ; Engineering and environment geology. Geothermics ; Exact sciences and technology ; Groundwater ; Groundwaters ; Isotopes ; Natural water pollution ; Olefins ; Pollution ; Pollution, environment geology ; tetrachloroethene ; Tetrachloroethylene - chemistry ; trichloroethene ; Trichloroethylene - chemistry ; USA, Delaware, Dover ; Water treatment and pollution</subject><ispartof>Environmental science & technology, 2001-01, Vol.35 (2), p.261-269</ispartof><rights>Copyright © 2001 American Chemical Society</rights><rights>2001 INIST-CNRS</rights><rights>Copyright American Chemical Society Jan 15, 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a466t-b9fd1d4f4986e17b0c92d8eae34617cad54a47568c9a5ddb6e1172f5bb4e7ad33</citedby><cites>FETCH-LOGICAL-a466t-b9fd1d4f4986e17b0c92d8eae34617cad54a47568c9a5ddb6e1172f5bb4e7ad33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/es001227x$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/es001227x$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=859864$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11347596$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sherwood Lollar, B</creatorcontrib><creatorcontrib>Slater, G. F</creatorcontrib><creatorcontrib>Sleep, B</creatorcontrib><creatorcontrib>Witt, M</creatorcontrib><creatorcontrib>Klecka, G. M</creatorcontrib><creatorcontrib>Harkness, M</creatorcontrib><creatorcontrib>Spivack, J</creatorcontrib><title>Stable Carbon Isotope Evidence for Intrinsic Bioremediation of Tetrachloroethene and Trichloroethene at Area 6, Dover Air Force Base</title><title>Environmental science & technology</title><addtitle>Environ. Sci. Technol</addtitle><description>Area 6 at Dover Air Force Base (Dover, DE) has been the location of an in-depth study by the RTDF (Remediation Technologies Development Forum Bioremediation of Chlorinated Solvents Action Team) to evaluate the effectiveness of natural attenuation of chlorinated ethene contamination in groundwater. Compound-specific stable carbon isotope measurements for dissolved PCE and TCE in wells distributed throughout the anaerobic portion of the plume confirm that stable carbon isotope values are isotopically enriched in 13C consistent with the effects of intrinsic biodegradation. During anaerobic microbial reductive dechlorination of chlorinated hydrocarbons, the light (12C) versus heavy isotope (13C) bonds are preferentially degraded, resulting in isotopic enrichment of the residual contaminant in 13C. To our knowledge, this study is the first to provide definitive evidence for reductive dechlorination of chlorinated hydrocarbons at a field site based on the δ13C values of the primary contaminants spilled at the site, PCE and TCE. For TCE, downgradient wells show δ13C values as enriched as −18.0‰ as compared to δ13C values for TCE in the source zone of −25.0 to −26.0‰. The most enriched δ13C value on the site was observed at well 236, which also contains the highest concentrations of cis-DCE, VC, and ethene, the daughter products of reductive dechlorination. Stable carbon isotope signatures are used to quantify the relative extent of biodegradation between zones of the contaminant plume. On the basis of this approach, it is estimated that TCE in downgradient well 236 is more than 40% biodegraded relative to TCE in the proposed source area.</description><subject>Applied sciences</subject><subject>Biodegradation</subject><subject>Biodegradation, Environmental</subject><subject>Bioremediation</subject><subject>Carbon</subject><subject>Carbon Isotopes - analysis</subject><subject>Chlorine compounds</subject><subject>Contamination</subject><subject>Delaware</subject><subject>Earth sciences</subject><subject>Earth, ocean, space</subject><subject>Engineering and environment geology. 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F</au><au>Sleep, B</au><au>Witt, M</au><au>Klecka, G. M</au><au>Harkness, M</au><au>Spivack, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stable Carbon Isotope Evidence for Intrinsic Bioremediation of Tetrachloroethene and Trichloroethene at Area 6, Dover Air Force Base</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2001-01-15</date><risdate>2001</risdate><volume>35</volume><issue>2</issue><spage>261</spage><epage>269</epage><pages>261-269</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><coden>ESTHAG</coden><abstract>Area 6 at Dover Air Force Base (Dover, DE) has been the location of an in-depth study by the RTDF (Remediation Technologies Development Forum Bioremediation of Chlorinated Solvents Action Team) to evaluate the effectiveness of natural attenuation of chlorinated ethene contamination in groundwater. Compound-specific stable carbon isotope measurements for dissolved PCE and TCE in wells distributed throughout the anaerobic portion of the plume confirm that stable carbon isotope values are isotopically enriched in 13C consistent with the effects of intrinsic biodegradation. During anaerobic microbial reductive dechlorination of chlorinated hydrocarbons, the light (12C) versus heavy isotope (13C) bonds are preferentially degraded, resulting in isotopic enrichment of the residual contaminant in 13C. To our knowledge, this study is the first to provide definitive evidence for reductive dechlorination of chlorinated hydrocarbons at a field site based on the δ13C values of the primary contaminants spilled at the site, PCE and TCE. For TCE, downgradient wells show δ13C values as enriched as −18.0‰ as compared to δ13C values for TCE in the source zone of −25.0 to −26.0‰. The most enriched δ13C value on the site was observed at well 236, which also contains the highest concentrations of cis-DCE, VC, and ethene, the daughter products of reductive dechlorination. Stable carbon isotope signatures are used to quantify the relative extent of biodegradation between zones of the contaminant plume. On the basis of this approach, it is estimated that TCE in downgradient well 236 is more than 40% biodegraded relative to TCE in the proposed source area.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>11347596</pmid><doi>10.1021/es001227x</doi><tpages>9</tpages></addata></record> |
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subjects | Applied sciences Biodegradation Biodegradation, Environmental Bioremediation Carbon Carbon Isotopes - analysis Chlorine compounds Contamination Delaware Earth sciences Earth, ocean, space Engineering and environment geology. Geothermics Exact sciences and technology Groundwater Groundwaters Isotopes Natural water pollution Olefins Pollution Pollution, environment geology tetrachloroethene Tetrachloroethylene - chemistry trichloroethene Trichloroethylene - chemistry USA, Delaware, Dover Water treatment and pollution |
title | Stable Carbon Isotope Evidence for Intrinsic Bioremediation of Tetrachloroethene and Trichloroethene at Area 6, Dover Air Force Base |
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