2012
DOI: 10.1371/journal.pone.0033535
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Microbial Communities in Long-Term, Water-Flooded Petroleum Reservoirs with Different in situ Temperatures in the Huabei Oilfield, China

Abstract: The distribution of microbial communities in the Menggulin (MGL) and Ba19 blocks in the Huabei Oilfield, China, were studied based on 16S rRNA gene analysis. The dominant microbes showed obvious block-specific characteristics, and the two blocks had substantially different bacterial and archaeal communities. In the moderate-temperature MGL block, the bacteria were mainly Epsilonproteobacteria and Alphaproteobacteria , and the archaea were methanogens belonging to … Show more

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Cited by 84 publications
(87 citation statements)
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“…The most common Erysipelothrix tag sequence was 98 to 99% similar over its length (450 bp) to environmental sequences from a terrestrial mud volcano (42) and a terrestrial oil well (43) in China. Interestingly, both of these studies of subsurface habitats also detected Hydrogenophaga.…”
Section: Discussionmentioning
confidence: 88%
“…The most common Erysipelothrix tag sequence was 98 to 99% similar over its length (450 bp) to environmental sequences from a terrestrial mud volcano (42) and a terrestrial oil well (43) in China. Interestingly, both of these studies of subsurface habitats also detected Hydrogenophaga.…”
Section: Discussionmentioning
confidence: 88%
“…were relatively abundant (31.6% to 45.0% of the amplified Archaea 16S rRNA genes) in anaerobic digesters (cluster III sludge samples), and their abundances could be distinctively discriminated from other sources of sludge samples (0.7% to 6.5% of the amplified Archaea 16S rRNA genes, clusters I and II). In addition to reactor ecosystems, this methanogenic archaeon was present in natural environments (47)(48)(49). Its relatively extensive distribution suggests that this novel archaeon plays an important role in various methanogenic ecosystems.…”
Section: Discussionmentioning
confidence: 99%
“…DNA from the soil samples were subjected to both bacterial and archaeal T-RFLP analyses as previously described (Yu et al, 2010;Tang et al, 2012). Archaeal and bacterial small subunit ribosomal RNA (SSU rRNA) genes were amplified for T-RFLP analysis using the universal archaeal primers Arch109F (5 -ACK GCT CAG TAA CAC GT-3 ) and 5 6-carboxyfluorescein (FAM)-labeled Arch915R primer (5 -GTG CTC CCC CGC CAA TTC CT-3 ) (Lueders and Friedrich, 2003), and the universal bacterial primers 5 FAMlabeled 8F (5 -AGA GTT TGA TCC TGG CTC AG-3 ) and 1492R (5 -CGG TTA CCT TGT TAC GAC TT-3 ) (Dojka et al, 1998), respectively.…”
Section: Pcr Amplification and T-rflpmentioning
confidence: 99%