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Rapid shift from denitrification to nitrification in soil after biogas residue application as indicated by nitrous oxide isotopomers

机译:一氧化二氮异位异构体表明,施用沼气残渣后土壤中的反硝化作用迅速转变为硝化作用

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Nitrous oxide (N2O) is one of the major greenhouse gases emitted from soils, where it is mainly produced by nitrification and denitrification. It is well known that rates of N2O release from soils are mainly determined by the availability of substrates and oxygen, but N2O source apportioning, highly needed to advance N2O mitigation strategies, still remains challenging. In this study, using an automated soil incubation system, the N2O site preference, i.e. the intramolecular 1514 distribution, was analyzed to evaluate the progression in N2O source processes following organic soil amendment. Biogas fermentation residue (BGR; originating from food waste fermentation) was applied to repacked grassland soil cores and compared to ammonium sulfate (AS) application, both at rates equivalent to 160 kg NH4+-N ha(-1), and to unamended soil (control). The soil cores were incubated in a helium-oxygen atmosphere with 20 kPa O-2 for 43 days at 80% water-filled pore space. 43-day cumulative N2O emissions were highest with BGR treated soil accounting for about 1.68 kg N2O-N ha(-1) while application of AS caused much lower fluxes of c. 0.23 kg N2O-N ha(-1). Also, after BGR application, carbon dioxide (CO2) fluxes showed a pronounced initial peak with steep decline until day 21 whereas with ammonium addition they remained at the background level. N2O dual isotope and isotopomer analysis of gas samples collected from BGR treated soil indicated bacterial denitrification to be the main N2O generating process during the first three weeks when high CO2 fluxes signified high carbon availability. In contrast, in the second half after all added labile carbon substrates had been consumed, nitrification, i.e. the generation of N2O via oxidation of hydroxylamine, gained in importance reaching roughly the same N2O production rate compared to bacterial denitrification as indicated by N2O SP. Overall in this study, bacterial denitrification seemed to be the main N2O forming process after application of biogas residues and fluxes were mainly driven by available organic carbon
机译:一氧化二氮(N2O)是土壤排放的主要温室气体之一,主要通过硝化和反硝化作用产生。众所周知,N2O从土壤中释放的速率主要取决于底物和氧气的可用性,但是推进N2O缓解策略急需的N2O源分配仍然具有挑战性。在这项研究中,使用自动土壤培养系统,分析了N2O的位点偏好,即分子内1514分布,以评估有机土壤改良后N2O源过程的进展。将沼气发酵残留物(BGR;源自食物垃圾发酵)应用于重新包装的草原土壤核心,并与硫酸铵(AS)进行了比较,二者的施用量均相当于160 kg NH4 + -N ha(-1)和未经修正的土壤(控制)。将土壤核心在充有80%水的孔隙空间中于20 kPa O-2的氦氧气氛中孵育43天。 BGR处理过的土壤43天累积N2O排放量最高,约占1.68 kg N2O-N ha(-1),而AS的施用导致c的通量低得多。 0.23千克N2O-N ha(-1)。同样,在施用BGR后,二氧化碳(CO2)通量显示出明显的初始峰值,并急剧下降直至第21天,而添加铵时,它们仍保持在背景水平。从BGR处理过的土壤中收集的气体样品的N2O双重同位素和同位素分析表明,在高CO2通量表示高碳可利用量的前三周中,细菌反硝化作用是N2O的主要产生过程。相反,在所有添加的不稳定碳底物都被消耗完之后的下半年,硝化作用(即通过羟胺氧化产生N2O)的重要性与N2O SP所表明的细菌反硝化相比达到了大致相同的N2O生产率。总体而言,在这项研究中,细菌氮的反硝化似乎是沼气残留物施用后主要的N2O形成过程,而通量主要是由有效有机碳驱动

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