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N_2O, NH_3 AND NO_x EMISSIONS AS A FUNCTION OF UREA GRANULE SIZE AND SOIL TYPE UNDER AEROBIC CONDITIONS

机译:需氧条件下N_2O,NH_3和NO_x排放与尿素粒径和土壤类型的关系

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We examined the influence of various urea granule sizes ( < 2,7.0,9.9 and 12.7 mm) applied into a silt loam soil (experiment 1) and soil types (sandy, silt and clay loam) treated with the largest granule (experiment 2) on gaseous N loss (except N_2) at field capacity. The prilled urea (PU) was mixed into the soil whereas the urea granules were point-placed at a 5.0-cm depth. For experiment 1, N_2O emission was enhanced with increasing granule size, ranging from 0.17-0.50% of the added N during the 45-day incubation period. In the case of experiment 2, the sandy loam soil (0.59%) behaved similarly with the silt loam (0.53%) but both showed remarkably lower emissions than were found for the clay loam soil (2.61%). Both nitrification and N_2O emissions were delayed by several days with increasing granule size, and the latter was influenced by mineral N, soil water and pH. By contrast, the NH_3 volatilization decreased with increasing granule size, implying the inhibition of urease activity by urea concentration gradients. Considering both experimental results, the NH_3 loss was highest for the PU-treated (1.73%) and the larger granules regardless of soil type did not emit more than 0.27% of the added N over 22 days, possibly because the high concentrations of either mineral N or NH_4~+ in the soil surface layer (0-2.5 cm) and the high H~+ buffering capacity might regulate the NH_3 emission. Similar to the pattern of NH_3 loss, NO_x emission was noticeably higher for the PU-treated soil (0.97%) than for the larger granule sizes (0.09-0.29%), which were the highest for the sandy and clay loam soils. Positional differences in the concentration of mineral N and nitrification also influenced the NO_x emission. As such, total NH_3 loss was proportional to total NO_x emission, indicating similar influence of soil and environmental conditions on both. Pooled total N_2O, NH_3 and NO_x emission data suggest that the PU-treated soil could induce greater gaseous N loss over larger urea granules, largely in the form of NH_3 and NO_x emissions, whereas a similar increase with the largest granule size was mainly due to the total N_2O flux.
机译:我们研究了将不同大小的尿素颗粒(<2,7.0、9.9和12.7 mm)施用于粉壤土(实验1)和用最大颗粒处理的土壤类型(砂壤土,粉砂和粘土壤土)的影响(实验2)场容量下的气态氮损失(N_2除外)。将造粒的尿素(PU)混合到土壤中,而尿素颗粒则以5.0厘米深的点放置。对于实验1,N_2O排放随着颗粒大小的增加而增强,在45天的温育期内,N_2O的释放量为所添加氮的0.17-0.50%。在实验2的情况下,沙质壤土(0.59%)的行为与粉质壤土(0.53%)相似,但两者均显示出比粘土壤土(2.61%)低得多的排放。随着颗粒尺寸的增加,硝化作用和N_2O排放都延迟了几天,而后者受矿质氮,土壤水和pH值的影响。相反,随着颗粒尺寸的增加,NH_3挥发减少,这意味着尿素浓度梯度会抑制尿素酶的活性。考虑到这两个实验结果,PU处理的NH_3损失最高(1.73%),无论土壤类型如何,较大的颗粒在22天内排放的氮量都不超过0.27%,这可能是因为两种矿物质的浓度很高土壤表层(0-2.5 cm)中的N或NH_4〜+和高的H〜+缓冲能力可能会调节NH_3的释放。与NH_3的损失模式相似,PU处理的土壤(0.97%)的NO_x排放显着高于较大粒径的颗粒(0.09-0.29%),这对于沙质和壤土壤土来说最高。矿质氮浓度和硝化作用的位置差异也影响了NO_x的排放。因此,总的NH_3损失与总的NO_x排放成正比,表明土壤和环境条件对两者的影响相似。汇总的总N_2O,NH_3和NO_x排放数据表明,PU处理的土壤比较大的尿素颗粒可能以更大的NH_3和NO_x排放形式引起更大的气态N损失,而最大颗粒大小的类似增加主要是由于N_2O总通量。

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