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硝态氮异化还原机制及其主导因素研究进展
引用本文:杨杉,吴胜军,蔡延江,周文佐,朱同彬,王雨,黄平.硝态氮异化还原机制及其主导因素研究进展[J].生态学报,2016,36(5):1224-1232.
作者姓名:杨杉  吴胜军  蔡延江  周文佐  朱同彬  王雨  黄平
作者单位:中国科学院水库水环境重点实验室, 中国科学院重庆绿色智能技术研究院, 重庆 400714;西南大学地理科学学院, 重庆 400715,中国科学院水库水环境重点实验室, 中国科学院重庆绿色智能技术研究院, 重庆 400714,中国科学院水利部成都山地灾害与环境研究所中国科学院山地表生过程与生态调控重点实验室, 成都 610041,西南大学地理科学学院, 重庆 400715,南京师范大学地理科学学院, 南京 210046,中国科学院水库水环境重点实验室, 中国科学院重庆绿色智能技术研究院, 重庆 400714,中国科学院水库水环境重点实验室, 中国科学院重庆绿色智能技术研究院, 重庆 400714
基金项目:中国科学院西部行动计划项目(KZCX2-XB3-14); 重庆市基础与前沿研究项目(cstc2013jcyjA0302);中国科学院水库水环境重点实验室开放基金(RAE2014BA06B)
摘    要:硝态氮(NO_3~-)异化还原过程通常包含反硝化和异化还原为铵(DNRA)两个方面,是土壤氮素转化的重要途径,其强度大小直接影响着硝态氮的利用和环境效应(如淋溶和氮氧化物气体排放)。反硝化和DNRA过程在反应条件、产物和影响因素等方面常会呈现出协同与竞争的交互作用机制。综述了反硝化和DNRA过程的研究进展及其二者协同竞争的作用机理,并阐述了在NO_3~-、pH、有效C、氧化还原电位(Eh)等环境条件和土壤微生物对其发生强度和产物的影响,提出了今后应在产生机理、土壤环境因素、微生物学过程以及与其他氮素转化过程耦联作用等方面亟需深入研究,以期增进对氮素循环过程的认识以及为加强氮素管理利用提供依据。

关 键 词:硝态氮异化还原  反硝化  硝态氮异化还原成铵(DNRA)  N2O  协同竞争机制
收稿时间:2014/7/18 0:00:00
修稿时间:2015/12/10 0:00:00

The synergetic and competitive mechanism andthe dominant factors of dissimilatory nitrate reduction processes: a review
YANG Shan,WU Shengjun,CAI Yanjiang,ZHOU Wenzuo,ZHU Tongbin,WANG Yu and HUANG Ping.The synergetic and competitive mechanism andthe dominant factors of dissimilatory nitrate reduction processes: a review[J].Acta Ecologica Sinica,2016,36(5):1224-1232.
Authors:YANG Shan  WU Shengjun  CAI Yanjiang  ZHOU Wenzuo  ZHU Tongbin  WANG Yu and HUANG Ping
Institution:Key Laboratory of Reservoir Aquatic Environment, Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Science, Chongqing 400714, China;School of Geography Science, Southwest University, Chongqing 400715, China,Key Laboratory of Reservoir Aquatic Environment, Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Science, Chongqing 400714, China,Institute of Mountain Hazards and Environment, Chinese Academy of Sciences and Ministry of Water Resources; Key Laboratory of Mountain Environment Evolvement and Regulation, Chinese Academy of Sciences, Chengdu 610041, China,School of Geography Science, Southwest University, Chongqing 400715, China,College of Geography Science, Nanjing Normal University, Nanjing 210046, China,Key Laboratory of Reservoir Aquatic Environment, Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Science, Chongqing 400714, China and Key Laboratory of Reservoir Aquatic Environment, Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Science, Chongqing 400714, China
Abstract:The nitrate ion (NO3-), an important form of inorganic soil nitrogen, is susceptible to reduction under anaerobic conditions, and its reduction consists of both assimilatory and dissimilatory processes. The dissimilatory nitrate reduction process-of great significance in nitrogen transformation-includes denitrification and dissimilatory nitrate reduction to ammonium (DNRA). Such reduction processes can directly affect the transformation of nitrates and the environmental consequences (such as NO3- leaching and N2O emission). During the processes of denitrification and DNRA, NO3- is utilized as a substrate, while N2O is generated synchronously. Nonetheless, there are significant differences between denitrification and DNRA, such as metabolic processes, the transformation mechanism, reductases, and the final products. For DNRA, the final product is ammonium (NH4+), which can continue to participate in other soil nitrogen transformation processes, such as crop uptake and nitrification. In agroecosystems, DNRA can consume 3.9%-25.4% of NO3-; this process can decrease NO3- leaching and N2O emissions in comparison with denitrification.Both reducing pathways show a synergistic and competitive mechanism among the reaction conditions, products, and dominant regulators. The synergistic mechanism of denitrification and DNRA manifests itself as the similar suitable environmental conditions, the shared nitrate reductase (Nar), and an intermediate product (N2O), along with the similar soil parameters. Thus, according to the synergistic effect, the dissimilatory nitrate reduction process can be greatly enhanced without limiting factors such as the soil water regimen, temperature, and soil substrates. As for the competitive mechanism, it mainly involves competition for a substrate and energy supplies between denitrification and DNRA. In contrast, the direct competition for NO3- exists ubiquitouslybetween denitrification and DNRA. Nevertheless, regulation of soil parameters (such as available carbon,oxidation-reduction potential (Eh)) changes the concentration of NO3- accordingly; thus, the competition for NO3- between denitrification and DNRA should be rebalanced subsequently. Moreover, soil microorganisms that are related to denitrification and DNRA can compete for a carbon source for their growth and proliferation. The dissimilatory nitrate reduction process is influenced by a great number of factors, mainly environmental conditions and microorganisms. Sufficient soil NO3- and available carbon can significantly enhance the dissimilatory nitrate reduction process, whereas soil pH and Eh have their own suitable ranges for different dissimilatory nitrate reduction processes. The competition between denitrification and DNRA is regulated by these factors. With the changes in available carbon, soil pH, and Eh, the two pathways show different levels of activity. Bacteria can exist in the form of an advantageous microbial population during the dissimilatory nitrate reduction process. Nevertheless, different populations and genes are involved in denitrification and DNRA, and the diversity of soilmicroorganisms is in turn influenced by soil environmental factors. This review summarizes the synergistic and competitive mechanisms and the factors influencing denitrification and DNRA, for example, soil environmental conditions (soil NO3-, soil pH, available carbon and Eh) and microorganisms (population, diversity and genes). The mechanism of formation, soil environmental factors, microbiological processes, and the correlation with other nitrogen transformation processesurgently need further research on dissimilatory nitrate reduction processes. In DNRA, the mechanism of formation and analysis of N2O emissions, populations, diversity, and genes of a microorganism have not been established yet. In addition, the interactions of nitrogen transformation processes in soils-e.g., between denitrification and DNRA or between anaerobic ammonium oxidation and denitrification-should be investigated holistically. The knowledge about synergistic and competitive mechanisms and the factors influencing denitrification and DNRA should improve the understanding of the regulation of nitrogen transformation in soils; this knowledge is also necessary for the development of effective countermeasures and policies on soil nitrogen management.
Keywords:dissimilatorynitrate reduction process  denitrification  dissimilatory nitrate reduction to ammonium (DNRA)  N2O  synergetic and competitive mechanism
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