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Anaerobic Ammonium Oxidation in Acidic Red Soils

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2018 Sep 21
PMID 30233562
Citations 3
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Abstract

Anaerobic ammonium oxidation (anammox) has been proven to be an important nitrogen removal process in terrestrial ecosystems, particularly paddy soils. However, the contribution of anammox in acidic red soils to nitrogen loss has not been well-documented to date. Here, we investigated the activity, abundance, and distribution of anammox bacteria in red soils collected from nine provinces of Southern China. High-throughput sequencing analysis showed that Brocadia dominates the anammox bacterial community (93.03% of sequence reads). Quantification of the hydrazine synthase gene () and anammox 16S rRNA gene indicated that the abundance of anammox bacteria ranged from 6.20 × 10 to 1.81 × 10 and 4.81 × 10 to 4.54 × 10 copies per gram of dry weight, respectively. Contributions to nitrogen removal by anammox were measured by a N isotope-pairing assay. Anammox rates in red soil ranged from 0.01 to 0.59 nmol N g h, contributing 16.67-53.27% to N production in the studied area, and the total amount of removed nitrogen by anammox was estimated at 2.33 Tg N per year in the natural red soils of southern China. Pearson correlation analyses revealed that the distribution of anammox bacteria significantly correlated with the concentration of nitrate and pH, whereas the abundance and activity of anammox bacteria were significantly influenced by the nitrate and total nitrogen concentrations. Our findings demonstrate that Brocadia dominates anammox bacterial communities in acidic red soils and plays an important role in nitrogen loss of the red soil in Southern China.

Citing Articles

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Diversity and Distribution of Anaerobic Ammonium Oxidation Bacteria in Hot Springs of Conghua, China.

Liu L, Lv A, Rao M, Ming Y, Salam N, Li M Front Microbiol. 2022; 12:739234.

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Nitrification mainly driven by ammonia-oxidizing bacteria and nitrite-oxidizing bacteria in an anammox-inoculated wastewater treatment system.

Lu J, Hong Y, Wei Y, Gu J, Wu J, Wang Y AMB Express. 2021; 11(1):158.

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References
1.
Nicol G, Leininger S, Schleper C, Prosser J . The influence of soil pH on the diversity, abundance and transcriptional activity of ammonia oxidizing archaea and bacteria. Environ Microbiol. 2008; 10(11):2966-78. DOI: 10.1111/j.1462-2920.2008.01701.x. View

2.
Strous M, Kuenen J, Jetten M . Key physiology of anaerobic ammonium oxidation. Appl Environ Microbiol. 1999; 65(7):3248-50. PMC: 91484. DOI: 10.1128/AEM.65.7.3248-3250.1999. View

3.
Erguder T, Boon N, Wittebolle L, Marzorati M, Verstraete W . Environmental factors shaping the ecological niches of ammonia-oxidizing archaea. FEMS Microbiol Rev. 2009; 33(5):855-69. DOI: 10.1111/j.1574-6976.2009.00179.x. View

4.
Dang H, Zhou H, Zhang Z, Yu Z, Hua E, Liu X . Molecular detection of Candidatus Scalindua pacifica and environmental responses of sediment anammox bacterial community in the Bohai Sea, China. PLoS One. 2013; 8(4):e61330. PMC: 3620062. DOI: 10.1371/journal.pone.0061330. View

5.
Xi D, Bai R, Zhang L, Fang Y . Contribution of Anammox to Nitrogen Removal in Two Temperate Forest Soils. Appl Environ Microbiol. 2016; 82(15):4602-4612. PMC: 4984287. DOI: 10.1128/AEM.00888-16. View