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Methane, nitrogen monoxide, and nitrous oxide fluxes in an organic soil.

机译:甲烷,一氧化氮和一氧化二氮在有机土壤中的通量。

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Field and laboratory studies were performed to estimate fluxes of the a-ace gases nitrogen monoxide (NO), nitrous oxide (N2O), and methane (CH4) in an organic soil, to determine the microbial processes involved, and to assess how soil water and nitrogen controlled flux rates. Metabolic inhibitors showed microbial nitrification to be the major NO source, regardless of the soil moisture content. Nitrification also produced N 2O, but denitrification losses of this gas from flooded, anaerobic soil were much higher. Up to 26% of nitrified N was converted to NO, but most of this (95%) was consumed microbially before it could escape across the soil surface. The NO-consuming process appeared to be co-oxidation by soil heterotrophs, not coupled to energy production. Organic matter content and CO2 production were therefore good predictors of NO oxidation rates across soil types, and NO oxidation was stimulated by manure addition.; Soil water and nitrogen had nonlinear effects on trace gas fluxes, acting on both production and consumption. Kinetic analysis showed that nitrate was a weak noncompetitive inhibitor, but ammonium a strong competitive inhibitor of soil CH4 oxidation at field fertilization rates. However, spatial and temporal factors complicated fertilization effects on CH4 oxidation in situ. Ammonium was immobilized in surface soil and rapidly nitrified, limiting its inhibitory effect on CH 4 oxidation. Fertilizer N stimulated nitrification and denitrification and therefore gaseous N-oxide production, but other, unexpected fertilizer effects were also observed. Ammonium fertilizer decreased NO oxidation rates. Nitrate and other salts stimulated NO and N2O losses during nitrification, an effect apparently related to soil nitrite accumulation.; The controls exerted on trace gas fluxes by soil water were mediated primarily through diffusion rates. Oxygen diffusion controlled the balance of anaerobic (methanogenesis and denitrification) versus aerobic (CH 4 oxidation and nitrification) processes. Soil moisture content also controlled the diffusion rate of atmospheric CH4 to soil methanotrophs, and the escape of gaseous N-oxides from production sites across the soil surface.
机译:进行了现场和实验室研究,以估算有机土壤中a-ace气体一氧化氮(NO),一氧化二氮(N2O)和甲烷(CH4)的通量,以确定涉及的微生物过程,并评估土壤水分和氮气控制的通量率。无论土壤含水量如何,代谢抑制剂均显示微生物硝化作用是主要的NO来源。硝化作用还会产生N 2O,但是从充满水的厌氧土壤中产生的这种气体的反硝化损失要高得多。高达26%的硝化N转化为NO,但是其中大部分(95%)在被微生物消耗之前就已经被微生物消耗掉了。消耗NO的过程似乎是土壤异养菌的共氧化作用,与能源生产无关。因此,有机质含量和CO 2产生是不同土壤类型NO氧化速率的良好预测指标,并且通过添加肥料刺激NO氧化。土壤水和氮对痕量气体通量具有非线性影响,对生产和消费都有影响。动力学分析表明,在田间施肥时,硝酸盐是弱竞争性抑制剂,而铵盐是土壤CH4氧化的强竞争性抑制剂。但是,时空因素使施肥对CH4原位氧化的影响复杂化。铵被固定在表层土壤中并迅速硝化,从而限制了其对CH 4氧化的抑制作用。氮肥可促进硝化和反硝化作用,因此可产生气态氮氧化物,但同时也观察到其他意想不到的肥料作用。铵肥降低了NO的氧化速率。硝酸盐和其他盐类会在硝化过程中刺激NO和N2O的损失,这显然与土壤亚硝酸盐的积累有关。土壤水对微量气体通量的控制主要是通过扩散速率来介导的。氧扩散控制了厌氧(甲烷生成和反硝化)与好氧(CH 4氧化和硝化)过程之间的平衡。土壤含水量还控制着大气中CH4向甲烷甲烷营养菌的扩散速率,并控制了气态N-氧化物从整个土壤表面的生产场所逸出。

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