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施肥稻田中的厌氧氨氧化。

Anaerobic ammonia oxidation in a fertilized paddy soil.

机构信息

State Key Laboratory of Environmental Aquatic Quality, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, China.

出版信息

ISME J. 2011 Dec;5(12):1905-12. doi: 10.1038/ismej.2011.63. Epub 2011 May 19.

Abstract

Evidence for anaerobic ammonium oxidation in a paddy field was obtained in Southern China using an isotope-pairing technique, quantitative PCR assays and 16S rRNA gene clone libraries, along with nutrient profiles of soil cores. A paddy field with a high load of slurry manure as fertilizer was selected for this study and was shown to contain a high amount of ammonium (6.2-178.8  mg  kg(-1)). The anaerobic oxidation of ammonium (anammox) rates in this paddy soil ranged between 0.5 and 2.9  nmol N per gram of soil per hour in different depths of the soil core, and the specific cellular anammox activity observed in batch tests ranged from 2.9 to 21  fmol per cell per day. Anammox contributed 4-37% to soil N2 production, the remainder being due to denitrification. The 16S rRNA gene sequences of surface soil were closely related to the anammox bacteria 'Kuenenia', 'Anammoxoglobus' and 'Jettenia'. Most of the anammox 16S rRNA genes retrieved from the deeper soil were affiliated to 'Brocadia'. The retrieval of mainly bacterial amoA sequences in the upper part of the paddy soil indicated that nitrifying bacteria may be the major source of nitrite for anammox bacteria in the cultivated horizon. In the deeper oxygen-limited parts, only archaeal amoA sequences were found, indicating that archaea may produce nitrite in this part of the soil. It is estimated that a total loss of 76  g  N  m(-2) per year is linked to anammox in the paddy field.

摘要

在中国南方,采用同位素配对技术、定量 PCR 检测和 16S rRNA 基因克隆文库以及土壤芯养分剖面的方法,在稻田中获得了厌氧氨氧化的证据。选择了一个施浆肥负荷高的稻田进行这项研究,结果表明该稻田含有大量的铵(6.2-178.8mgkg(-1))。在土壤芯的不同深度,该稻田土壤中铵的厌氧氧化(anammox)速率在 0.5 至 2.9  nmol N 每克土壤每小时之间变化,批量测试中观察到的特定细胞 anammox 活性范围为 2.9 至 21  fmol 每个细胞每天。anammox 对土壤 N2 生成的贡献为 4-37%,其余部分归因于反硝化作用。表层土壤的 16S rRNA 基因序列与 anammox 细菌 'Kuenenia'、'Anammoxoglobus'和 'Jettenia'密切相关。从较深土壤中获得的大多数 anammox 16S rRNA 基因与 'Brocadia'有关。在稻田耕层上部主要回收细菌 amoA 序列表明,硝化细菌可能是耕层中 anammox 细菌亚硝酸的主要来源。在较深的氧气受限部分,只发现了古菌 amoA 序列,表明古菌可能在这部分土壤中产生亚硝酸。据估计,稻田中 anammox 每年导致 76  g  N  m(-2)的总损失。

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