Assessment of indigenous reductive dechlorinating potential at a TCE-contaminated site using microcosms, polymerase chain reaction analysis, and sitedata
De. Fennell et al., Assessment of indigenous reductive dechlorinating potential at a TCE-contaminated site using microcosms, polymerase chain reaction analysis, and sitedata, ENV SCI TEC, 35(9), 2001, pp. 1830-1839
Citations number
37
Categorie Soggetti
Environment/Ecology,"Environmental Engineering & Energy
A combination of microcosm studies, polymerase chain reaction (PCR) analysi
s, and site data was used to assess the indigenous reductive dechlorinating
potential in a trichloroethene (TCE)-contaminated aquifer at Ca pe Canaver
al Air Station, Florida. Sediment and groundwater were obtained from two di
stinct locations approximately 10 m apart, Microcosm studies were performed
to assess dechlorinating activity under a variety of nutrient and electron
donor amendment conditions. Most live microcosms constructed using materia
l from the first location, near well 9 (W09), were negative for dechlorinat
ion. All live microcosms constructed using material from the second locatio
n (W06) exhibited dechlorination of TCE to vinyl chloride (VC) and ethene (
ETH). DNA encoding 16S ribosomal RNA (rDNA) with a sequence nearly identica
l with that from Dehalococcoides ethenogenes strain 195 was detected in the
active microcosms and in the sediment from W06 with polymerase chain react
ion (PCR) using primers targeted to unique regions of Dehalococcoides 16S r
DNA. Dehalococcoides was not detected in the autoclaved microcosms from W06
, nor in sediment and most microcosms from W09. The results of the microcos
m studies and PCR analysis were supported by field data, which indicated si
gnificant accumulation of cis-1,2-dichloroethene (cisDCE) and VC at W06, bu
t not at W09, The different microcosm results obtained far the two location
s and the spatial variation of positive PCR results indicates heterogeneous
distribution of dechlorinating activity and a specific dechlorinating orga
nism, Dehalococcoides, at the site. As both Dehalococcoides and dechlorinat
ion activity were similarly, heterogeneously distributed, this suggests tha
t molecular-probing (which could and should be extended in the future to in
clude virtually all known dechlorinators and/or dehalogenases) can provide
a relatively quick and facile method far investigating spatial distribution
s of dechlorinators on-site.