• ISSN 1008-505X
  • CN 11-3996/S
邢志强, 左继超, 付庆灵, 胡红青, 朱俊. 水钠锰矿提高红壤性水稻土N2O释放速率和氨氧化细菌amoA基因丰度[J]. 植物营养与肥料学报, 2020, 26(6): 1156-1164. DOI: 10.11674/zwyf.20002
引用本文: 邢志强, 左继超, 付庆灵, 胡红青, 朱俊. 水钠锰矿提高红壤性水稻土N2O释放速率和氨氧化细菌amoA基因丰度[J]. 植物营养与肥料学报, 2020, 26(6): 1156-1164. DOI: 10.11674/zwyf.20002
XING Zhi-qiang, ZUO Ji-chao, FU Qing-ling, HU Hong-qing, ZHU Jun. Birnessite increases N2O release rate and amoA gene abundance of ammonia-oxidizing bacteria in red paddy soil[J]. Journal of Plant Nutrition and Fertilizers, 2020, 26(6): 1156-1164. DOI: 10.11674/zwyf.20002
Citation: XING Zhi-qiang, ZUO Ji-chao, FU Qing-ling, HU Hong-qing, ZHU Jun. Birnessite increases N2O release rate and amoA gene abundance of ammonia-oxidizing bacteria in red paddy soil[J]. Journal of Plant Nutrition and Fertilizers, 2020, 26(6): 1156-1164. DOI: 10.11674/zwyf.20002

水钠锰矿提高红壤性水稻土N2O释放速率和氨氧化细菌amoA基因丰度

Birnessite increases N2O release rate and amoA gene abundance of ammonia-oxidizing bacteria in red paddy soil

  • 摘要:
    目的 土壤中的氧化亚氮 (N2O) 来源于硝化与反硝化作用,锰可与硝化或反硝化作用产物反应产生N2O或氮气,已有研究表明土壤中锰含量高会影响硝化作用。因此,本试验以水钠锰矿 (KMnO2·H2O) 与土壤硝化作用与反硝化作用的生物化学耦合反应为切入点,研究水钠锰矿的添加对土壤N2O释放速率及微生物的影响,进一步认识N2O释放与土壤环境因子的相互关系。
    方法 以红壤性水稻土为供试土壤,通过微宇宙培养试验,在土壤中添加不同质量百分比的水钠锰矿 (0%、0.1%、0.3%、0.7%、1.5%),预培养7 天后,加入硫酸铵N 100 mg/kg继续培养14天。在培养第1、3、7、14天,采用气密性注射器抽取10 mL气体样品,气相色谱仪测定N2O含量;同时取土壤样品,比色法测定铵态氮与硝态氮含量。培养结束时,测定土壤pH,采用实时荧光定量PCR测定土壤16S rDNA与氨氧化细菌 (AOB) amoA基因拷贝数,高通量测序技术分析微生物群落组成及多样性。
    结果 水钠锰矿提高了土壤N2O释放速率,增加了土壤N2O累积释放量,以添加0.1%水钠锰矿的N2O累积释放量最高,添加1.5%的最低。土壤铵态氮含量随培养时间的延长而迅速降低,硝态氮含量则迅速增加。水钠锰矿显著提高了土壤pH与表观N2O产量 (N2O-N/NO3-N),pH随着水钠锰矿添加量的增加整体提高,N2O-N/NO3-N则随着水钠锰矿添加量的增加呈降低趋势。适量水钠锰矿显著增加了土壤细菌16S rDNA与氨氧化细菌 (AOB) amoA基因拷贝数,并显著提高了土壤16S rDNA与AOB amoA基因拷贝数的比值,但随着水钠锰矿添加量的增加,细菌16S rDNA和AOB amoA基因拷贝数的增加量整体降低;放线菌、变形菌与拟杆菌是所有处理中的优势菌门,通过非度量多维尺度分析发现不同处理间的微生物群落结构差异显著,未添加水钠锰矿处理与添加水钠锰矿1.5%处理的微生物群落结构差异最大,其他处理的微生物群落结构介于两者之间。
    结论 土壤中添加0.1%质量比的水钠锰矿,可以通过增加AOB的数量促进红壤性水稻土N2O的释放,显著影响微生物物种丰度与群落结构。但水钠锰矿高添加量处理对AOB的刺激作用减弱,因此,应将土壤锰含量作为影响土壤N2O释放的因素加以考虑。

     

    Abstract:
    Objectives Nitrous oxide (N2O) in soil is a product of nitrification and denitrification, while manganese can react with the products of nitrification or denitrification to produce N2O or N2. Studies have shown that high levels of manganese can affect soil nitrification. Therefore, in this experiment the biochemical coupling reactions of manganese with soil nitrification and denitrification are considered as an entry point to study the effect of manganese addition on soil N2O release rate and microorganisms, so as to provide a new perspective to understand the interaction between N2O release and soil environmental factors.
    Methods A microcosmic incubation was conducted, using red paddy soil as tested material. Birnessite was added by 0, 0.1%, 0.3%, 0.7%, 1.5% into the soils, and pre-incubated for 7 days. Ammonium sulfate was then added in rate of N 100 mg/kg in each well and incubated for another14 days. On the 1st, 3rd, 7th, and 14th day of incubation, gas sample of 10 mL was collected using gas-tight syringe from each treatment and the N2O content was determined with gas chromatography. At the same time, soil samples were collected, the ammonium and nitrate nitrogen contents in the soil were determined by colorimetric method, the 16S rDNA and ammonia oxidizing bacteria (AOB) amoA gene copy numbers by real-time fluorescent quantitative PCR, and the composition and diversities of microbial communities were explored by high throughput sequencing technology.
    Results The addition of 0.1% birnessite increased the release rate and the accumulative emission of N2O from soil and also significantly increased soil pH and apparent N2O yield (N2O-N/NO3-N). In all treatments, the soil ammonium nitrogen decreased rapidly with the cultivation time, but the nitrate nitrogen content was reversed. Birnessite significantly increased the copy number of soil bacteria 16S rDNA and ammonia-oxidizing bacteria (AOB) amoA gene, and significantly increased the ratio of soil 16S rDNA to AOB amoA gene copy number. However, these promotion effects were not found when the addition rate of birnessite was higher than 0.1%. Actinomycetes, proteobacteria and bacteroides were the dominant phylums in all treatments. According to the result of non-metric multi-dimensional analysis, the microbial communities varied significantly among the treatments, with the largest discrepancy between the 0% treatment and the 1.5% treatment.
    Conclusions Low addition percentage of birnessite could increase the N2O release from the red paddy soil by increasing the amount of AOB, and affecting microbial species abundance and community structure. High addition rate did not show the effect as respected. Therefore, soil manganese content should be considered as the influencing factor of soil N2O release.

     

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