2016
DOI: 10.1080/01490451.2016.1159767
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Microbial Community Structure Associated with Biogeochemical Processes in the Sulfate–Methane Transition Zone (SMTZ) of Gas-hydrate-bearing Sediment of the Ulleung Basin, East Sea

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Cited by 15 publications
(7 citation statements)
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“…dsrB gene OTUs affiliated with Syntrophobacterales, Group I, Group II and Group III were detected in both QZM and DJ. Syntrophobacterales was comprised of 38% of the total dsrB genes, which were closely related to those retrieved from Three Gorge Reservoir, Evander Mine and Mafic sill ( Figure S1 ) [ 29 ]. The dsrB gene OTUs affiliated with the unclassified Group I, Group II and Group III showed no relationship to any known dsrB gene sequences and thus the unclassified Group I, Group II and Group III may be novel Deltaproteobacteria lineages.…”
Section: Resultsmentioning
confidence: 99%
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“…dsrB gene OTUs affiliated with Syntrophobacterales, Group I, Group II and Group III were detected in both QZM and DJ. Syntrophobacterales was comprised of 38% of the total dsrB genes, which were closely related to those retrieved from Three Gorge Reservoir, Evander Mine and Mafic sill ( Figure S1 ) [ 29 ]. The dsrB gene OTUs affiliated with the unclassified Group I, Group II and Group III showed no relationship to any known dsrB gene sequences and thus the unclassified Group I, Group II and Group III may be novel Deltaproteobacteria lineages.…”
Section: Resultsmentioning
confidence: 99%
“…Sulfate concentration was considered an important environmental factor affecting the rate of sulfate reduction and the abundance of SRB. On the other hand, the sulfate concentration also affected the diversity of the sulfate-reducing community, with a low sulfate concentration, the Firmicutes -like group was the predominant sulfate reducer at 0.8 mbsf in the SMTZ [ 29 ]. Sulfate concentration was important factor shaping the distribution of dsrB gene diversity in the Tibetan hot springs.…”
Section: Discussionmentioning
confidence: 99%
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“…Relationships between the microbial structure and distribution and hydrated methane in deep marine sediments have received worldwide attention. Extensive studies have been conducted to characterize microbial diversity, activity and importance in methane hydrate-bearing subseafloor sediments, such as those in the Cascadia Margin ( Cragg et al, 1995 ; Bidle et al, 1999 ; Lanoil et al, 2001 , 2005 ; Marchesi et al, 2001 ; Mills et al, 2003 , 2005 ; Knittel et al, 2005 ; Inagaki et al, 2006 ; Nunoura et al, 2008 ), Nankai Trough ( Reed et al, 2002 ; Kormas et al, 2003 ; Newberry et al, 2004 ; Mills et al, 2012 ; Katayama et al, 2016 , 2022 ), East Japan Sea ( Yanagawa et al, 2014 ), Andaman Sea ( Briggs et al, 2012 ), Ulleung Basin ( Jeong et al, 2010 ; Lee et al, 2013 ; Ryu et al, 2013 ; Cho et al, 2017 ), Arctic ( Carrier et al, 2020 ) and Shenhu area of the South China Sea ( Liao et al, 2009 ; Lin et al, 2014 ; Jiao et al, 2015 ; Cui et al, 2019 , 2020 ). A few of these studies were performed to compare the microbial communities in marine sediments with or without gas hydrate ( Inagaki et al, 2006 ; Yanagawa et al, 2014 ; Jiao et al, 2015 ; Cui et al, 2020 ).…”
Section: Introductionmentioning
confidence: 99%
“…2% of the global atmospheric CH 4 budget [ 5 , 6 ]. In such conditions, usually microbial consortia of anaerobic methanotrophic Archaea and sulfate-reducing bacteria [ 7 ] and/or Chloroflexi and Gammaproteobacteria [ 8 ], Proteobacteria, Elusimicrobia, and Actinobacteria [ 2 ] are identified. Cyanobacteria, Deferribacteres, and Thaumarchaeota are also abundant, although the taxonomic richness within these phyla is smaller [ 2 ] than in the phyla mentioned above.…”
Section: Introductionmentioning
confidence: 99%