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BTEX biodegradation is linked to bacterial community assembly patterns in contaminated groundwater ecosystem.
J. Hazard. Mater. 419:126205 (2021)
The control of degrader populations and the stochasticity and certainty of the microbial community in contaminated groundwater are not well-understood. In this study, a long-term contaminated groundwater ecosystem was selected to investigate the impact of BTEX on microbial communities and how microbial communities respond to BTEX pollution. 16S rRNA gene sequencing and metagenomic sequencing provided insights on microbial community assemblage patterns and their role in BTEX cleaning. The operational taxonomy units (OTUs) in the contaminated groundwater ecosystem were clustered distinguishably between the Plume and the Deeper Zone (lower contaminated zone). βNTI analysis revealed that the assembly strategies of abundant and rare OTU subcommunities preferred deterministic processes. Redundancy Analysis (RDA) and mantel testing indicated that benzene, toluene, ethylbenzene, and xylenes (BTEX) strongly drove the abundant OTU subcommunity, while the rare OTU subcommunity was only weakly affected. Deltaproteobacteria, the most dominant degrading microorganism, contains the complete degradation genes in the plume layer. In summary, our finding revealed that BTEX was the major factor in shaping the microbial community structure, and functional bacteria contribute greatly to water cleaning. Investigating the pattern of microbial community assembly will provide insights into the ecological controls of contaminant degradation in groundwater.
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Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Anaerobic Degradation ; Assembly Pattern ; Btex ; Microbial Community; Long-term; Microbial Community; Soil; Degradation; Aquifer; Fertilization; Biodiversity; Dispersal; Rare
Language
english
Publication Year
2021
HGF-reported in Year
2021
ISSN (print) / ISBN
0304-3894
e-ISSN
1873-3336
Journal
Journal of Hazardous Materials
Quellenangaben
Volume: 419,
Article Number: 126205
Publisher
Elsevier
Publishing Place
Radarweg 29, 1043 Nx Amsterdam, Netherlands
Reviewing status
Peer reviewed
Institute(s)
Institute of Virology (VIRO)
POF-Topic(s)
30203 - Molecular Targets and Therapies
Research field(s)
Immune Response and Infection
PSP Element(s)
G-554300-001
Grants
Chinese Scholarship Council, China
German Research Foundation, Germany (DFG)
German Research Foundation, Germany (DFG)
WOS ID
WOS:000693460200004
Scopus ID
85109198011
PubMed ID
34216964
Erfassungsdatum
2021-07-22