Stable carbon isotope fractionation during aerobic and anaerobic transformation of trichlorobenzene
FEMS Microbiology Ecology, ISSN: 0168-6496, Vol: 48, Issue: 3, Page: 313-321
2004
- 55Citations
- 39Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations55
- Citation Indexes55
- 55
- CrossRef38
- Captures39
- Readers39
- 39
Article Description
Fractionation of stable carbon isotopes upon degradation of trichlorobenzenes was studied under aerobic and anaerobic conditions. Mineralization of 1,2,4-trichlorobenzene by the aerobic strain Pseudomonas sp. P51 which uses a dioxygenase for the initial enzymatic reaction was not accompanied by a significant isotope fractionation. In contrast, reductive dehalogenation by the anaerobic strain Dehalococcoides sp. strain CBDB1 revealed average isotope enrichment factors ( ε ) between −3.1 and −3.7 for 1,2,3- and 1,2,4-trichlorobenzene, respectively. The significant isotope fractionation during reductive dehalogenation would allow tracing the in situ biodegradation of halogenated benzenes in contaminated anoxic aquifers, whereas the lack of isotope fractionation during aerobic transformation limits the use of this approach in oxic environments.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0168649604000583; http://dx.doi.org/10.1016/j.femsec.2004.02.005; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=2442551474&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/19712301; http://linkinghub.elsevier.com/retrieve/pii/S0168649604000583; http://dx.doi.org/10.1016/s0168-6496(04)00058-3; https://academic.oup.com/femsec/article-lookup/doi/10.1016/j.femsec.2004.02.005; http://dx.doi.org/10.1016/s0168-6496%2804%2900058-3; https://dx.doi.org/10.1016/s0168-6496%2804%2900058-3; https://academic.oup.com/femsec/article/48/3/313/583007; https://dx.doi.org/10.1016/j.femsec.2004.02.005
Oxford University Press (OUP)
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