2021
DOI: 10.1016/j.scitotenv.2021.146771
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Microbial community and abiotic effects on aquatic bacterial communities in north temperate lakes

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Cited by 30 publications
(28 citation statements)
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“…We collected 2 samples per location and time and found that replicates had no significant differences in the BCC ( p > 0.05). We also observed no significant replicate effect with 3–9 samples/location in our recently published study of aquatic bacterial community dynamics in north temperate lakes [ 17 ], thus we combined sequence read data of the two replicates for each week at each location to increase the read depth for all further statistical analyses.…”
Section: Resultsmentioning
confidence: 99%
“…We collected 2 samples per location and time and found that replicates had no significant differences in the BCC ( p > 0.05). We also observed no significant replicate effect with 3–9 samples/location in our recently published study of aquatic bacterial community dynamics in north temperate lakes [ 17 ], thus we combined sequence read data of the two replicates for each week at each location to increase the read depth for all further statistical analyses.…”
Section: Resultsmentioning
confidence: 99%
“…It has been postulated that local environmental processes and geographic distances (dispersal related) factors are potential mechanisms in structuring microbial biogeography ( Liu et al, 2019 ; Sadeghi et al, 2021 ). Environmental processes include abiotic (e.g., nutrients) and biotic (e.g., predation and competition) factors that regulate the community structure ( Zhou and Ning, 2017 ).…”
Section: Introductionmentioning
confidence: 99%
“…Bacterial DNA extraction and 16S rRNA gene library preparation DNA was extracted from fish hindgut content using a sucrose lysis buffer solution method previously described (Shahraki et al, 2019) and extracted DNA was subsequently stored at -20 degC, until further analysis. Additionally, the PCR conditions and 16S rRNA primer sets (1st and second PCR) were the same as those used in previously described methods (Sadeghi et al, 2021). Briefly, 16S rRNA variable regions of V5-V6 were amplified with a PCR cycle program of 95 degC for 3 min followed by 28 cycles of 95 degC for 30 s, 55 degC for 30 s, and 72 degC for 1 m, and a final step at 72 degC for 7 m. A second short-cycle PCR (7 cycles) using purified first PCR products ligated the adaptor and barcode (10 -12 bp) sequences to the amplicons as required for sample identification and sequencing.…”
Section: Lab Analysesmentioning
confidence: 99%