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Co-Occurring Anammox Denitrification and Codenitrification in Agricultural Soils

机译:农业土壤中同时发生的厌氧氨氧化反硝化和共硝化

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摘要

Anammox and denitrification mediated by bacteria are known to be the major microbial processes converting fixed N to N2 gas in various ecosystems. Codenitrification and denitrification by fungi are additional pathways producing N2 in soils. However, fungal codenitrification and denitrification have not been well investigated in agricultural soils. To evaluate bacterial and fungal processes contributing to N2 production, molecular and 15N isotope analyses were conducted with soil samples collected at six different agricultural fields in the United States. Denitrifying and anammox bacterial abundances were measured based on quantitative PCR (qPCR) of nitrous oxide reductase (nosZ) and hydrazine oxidase (hzo) genes, respectively, while the internal transcribed spacer (ITS) of Fusarium oxysporum was quantified to estimate the abundance of codenitrifying and denitrifying fungi. 15N tracer incubation experiments with 15NO3 or 15NH4+ addition were conducted to measure the N2 production rates from anammox, denitrification, and codenitrification. Soil incubation experiments with antibiotic treatments were also used to differentiate between fungal and bacterial N2 production rates in soil samples. Denitrifying bacteria were found to be the most abundant, followed by F. oxysporum based on the qPCR assays. The potential denitrification rates by bacteria and fungi ranged from 4.118 to 42.121 nmol N2-N g−1 day−1, while the combined potential rates of anammox and codenitrification ranged from 2.796 to 147.711 nmol N2-N g−1 day−1. Soil incubation experiments with antibiotics indicated that fungal codenitrification was the primary process contributing to N2 production in the North Carolina soil. This study clearly demonstrates the importance of fungal processes in the agricultural N cycle.
机译:细菌介导的厌氧氨氧化和反硝化作用是在各种生态系统中将固定氮转化为氮气的主要微生物过程。真菌的共硝化作用和反硝化作用是在土壤中产生N2的其他途径。但是,真菌共硝化和反硝化在农业土壤中尚未得到很好的研究。为了评估促成N2产生的细菌和真菌过程,对在美国六个不同农业领域收集的土壤样品进行了分子和 15 N同位素分析。分别基于一氧化二氮还原酶(nosZ)和肼氧化酶(hzo)基因的定量PCR(qPCR)测量反硝化和厌氧菌的细菌丰度,同时对尖孢镰刀菌的内部转录间隔区(ITS)进行定量,以评估可共硝化的细菌的丰度和反硝化真菌。添加了 15 NO3 - 15 NH4 + 15 N示踪剂孵育实验用来测量厌氧氨氧化法,反硝化法和共硝化法生产的氮气的生产率。用抗生素处理的土壤温育实验也用于区分土壤样品中真菌和细菌氮的产生速率。根据qPCR分析,发现反硝化细菌含量最高,其次是尖孢镰刀菌。细菌和真菌的潜在反硝化率范围为4.118至42.121 nmol N2-N g -1 day -1 ,而厌氧氨氧化法和共硝化作用的总反硝化率范围为2.796至147.711 nmol N2-N g -1 -1 。用抗生素进行的土壤温育实验表明,真菌共硝化作用是导致北卡罗莱纳州土壤中N2产生的主要过程。这项研究清楚地证明了真菌过程在农业氮素循环中的重要性。

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