2022
DOI: 10.1016/j.scitotenv.2022.155671
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Organo-mineral complexes alter bacterial composition and induce carbon and nitrogen cycling in the rhizosphere

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Cited by 12 publications
(7 citation statements)
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“…When β-NTI > 2 or β-NTI < −2, it indicates that the actual phylogenetic turnover between two communities is higher or lower than the expected phylogenetic turnover, i.e., the deterministic process dominates the structural changes; when −2 < β-NTI < 2, it indicates that the actual phylogenetic turnover between the two communities is similar to the expected phylogenetic turnover, i.e., the stochastic process dominates the structural changes (Anderson et al, 2011 ; Zheng et al, 2022 ). The difference between |β-NTI| and 0 represents the degree of clustering or dispersion of the system, that is, the impact of deterministic or stochastic processes on structural changes within a community.…”
Section: Methodsmentioning
confidence: 99%
“…When β-NTI > 2 or β-NTI < −2, it indicates that the actual phylogenetic turnover between two communities is higher or lower than the expected phylogenetic turnover, i.e., the deterministic process dominates the structural changes; when −2 < β-NTI < 2, it indicates that the actual phylogenetic turnover between the two communities is similar to the expected phylogenetic turnover, i.e., the stochastic process dominates the structural changes (Anderson et al, 2011 ; Zheng et al, 2022 ). The difference between |β-NTI| and 0 represents the degree of clustering or dispersion of the system, that is, the impact of deterministic or stochastic processes on structural changes within a community.…”
Section: Methodsmentioning
confidence: 99%
“…The V3–V4 region of 16S was amplified using the prime pair of 338F-806R (5′- ACTCCTACGGGAGGCAGCAG-3′ and 5′- GGACTACHVGGGTWTCTAAT-3′) for bacteria, while the ITS region was amplified using the prime pair of ITS1F-ITS2R (5′-CTTGGTCATTTAGAGAGGAAGTAA-3′ and 5′-GCTGCGTTCTTCATCGATGC-3′) for fungi . The PCR amplification process was followed by 3 min of denaturation at 95 °C, followed by 27 cycles of denaturation at 95 °C for 30 s, annealing at 55 °C for 30 s, and extension at 72 °C for 30 s. A final extension step of 10 min was done at 72 °C . Each sample was replicated 8 times, and sequencing was performed at Majorbio BioPharm Technology Co. Sequence data were submitted to the NCBI Sequence Read Archive under Bioproject PRJNA992782 and BioSample accession SAMN36374248.…”
Section: Methodsmentioning
confidence: 99%
“…5 The PCR amplification process was followed by 3 min of denaturation at 95 °C, followed by 27 cycles of denaturation at 95 °C for 30 s, annealing at 55 °C for 30 s, and extension at 72 °C for 30 s. A final extension step of 10 min was done at 72 °C. 19 Each sample was replicated 8 times, and sequencing was performed at Majorbio BioPharm Technology Co. Sequence data were submitted to the NCBI Sequence Read Archive under Bioproject PRJNA992782 and BioSample accession SAMN36374248.…”
Section: Microbial Analysismentioning
confidence: 99%
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