2018
DOI: 10.1029/2017jg004182
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Shifts in the Community Dynamics and Activity of Ammonia‐Oxidizing Prokaryotes Along the Yangtze Estuarine Salinity Gradient

Abstract: Ammonia oxidation, the first and rate-limiting step in nitrification, plays a critical role in the nitrogen cycle. However, the links between the dynamics of ammonia-oxidizing communities and ecosystem processes along the estuarine salinity gradient remain uncertain. In this study, we examined the diversity, abundance, and community structure of ammonia-oxidizing prokaryotes, and the potential nitrification rates along the Yangtze estuarine salinity gradient. Phylogenetic analysis showed that the predominant a… Show more

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Cited by 21 publications
(9 citation statements)
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References 69 publications
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“…Pearson correlation analyses were conducted to test correlations between diversity, abundance and environmental factors. One-way analysis of variance (ANOVA) tests were performed to compare PNRs rates ( Gao et al, 2016a ). Significance for all tests was accepted at p ≤ 0.05.…”
Section: Methodsmentioning
confidence: 99%
“…Pearson correlation analyses were conducted to test correlations between diversity, abundance and environmental factors. One-way analysis of variance (ANOVA) tests were performed to compare PNRs rates ( Gao et al, 2016a ). Significance for all tests was accepted at p ≤ 0.05.…”
Section: Methodsmentioning
confidence: 99%
“…Gao et al 44 also found that AOA community diversity increased as soil salinity increased, while AOB community diversity was highest in moderate or lower salinity soils. Alternatively, AOA communities can be adapted to low pH and low nutrient soil conditions 34,[45][46][47] , while AOB are thought to preferentially inhabit soil with neutral pH and high-N agricultural soils 10,44 . Following these observations, Schauss et al 48 speculated that AOB mainly dominate "nutrient-rich" environments, while AOA are better adapted to "nutrient-poor" environments.…”
Section: Discussionmentioning
confidence: 92%
“…All q-PCRs were performed in triplicate with an ABI 7500 Detection System (Applied Biosystems, Canada) using the SYBR Green method. The primers Arch-amoAF (STAATGGTCTGGCTTAGACG) and Arch-amoAR (GCGGCCATCCATCTGTATGT) were used to quantify the abundance of the AOA amoA gene (Gao et al, 2018), the primers amoA-1F (GGGGTTTCTACTGGTGGT) and amoA-2R (CCCCTCKGSAAAGCCTTCTTC) were used to quantify the abundance of the AOB amoA gene (Rotthauwe et al, 1997), the primers F1aCu (ATCATGGTSCTGCCGCG) and R3Cu (GCCTCGATCAGRTTGTGGTT) were used to quantify the abundance of the nirK gene (Hallin and Lindgren, 1999) and the primers cd3aF(GTSAACGTSAAGGARACSGG) and R3cd (GASTTCGGRTGSGTCTTGA) were used to quantify the abundance of the nirS gene (Throbäck et al, 2004). Details regarding the q-PCR conditions for these genes are provided in Table S1.…”
Section: Dna Isolation and Quantitative Pcrmentioning
confidence: 99%