Ti Chaopu, Ma Shutan, Peng Lingyun, Tao Limin, Wang Xi, Dong Wenxu, Wang Liangjie, Yan Xiaoyuan
State Key Laboratory of Soil and Sustainable Agriculture, Changshu National Agro-Ecosystem Observation and Research Station, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, 210008, China.
School of Environmental Science and Engineering, Anhui Normal University, Wuhu, 241002, China.
Environ Pollut. 2021 Feb 1;270:116204. doi: 10.1016/j.envpol.2020.116204. Epub 2020 Dec 7.
Ammonia (NH) volatilized from soils plays an important role in N cycle and air pollution, thus it is important to trace the emission source and predict source contributions to development strategies mitigating the environmental harmful of soil NH volatilization. The measurements of N natural abundance (δN) could be used as a complementary tool for apportioning emissions sources to resolve the contribution of multiple NH emission sources to air NH pollution. However, information of the changes of δN-NH values during the whole volatilization process under different N application rates are currently lacking. Hence, to fill this gap, we conducted a 15-day incubation experiment included different urea-N application rates to determine δN values of NH during volatilization process. Results showed that volatilization process depleted N in NH. The average δN value of NH volatilized from the 0, 20, 180, and 360 kg N ha treatment was -16.2 ± 7.3‰, -26.0 ± 5.4‰, -34.8 ± 4.8‰, and -40.6 ± 5.7‰. Overall, δN-NH values ranged from -46.0‰ to -4.7‰ during the whole volatilization process, with lower in higher urea-N application treatments than those in control. δN-NH values during the NH volatilization process were much lower than those of the primary sources, soil (-3.4 ± 0.1‰) and urea (-3.6 ± 0.1‰). Therefore, large isotopic fractionation may occur during soil volatilization process. Moreover, negative relationships between soil NH-N and NH volatilization rate and δN-NH values were observed in this study. Our results could be used as evidences of NH source apportionments and N cycle.
从土壤中挥发的氨(NH₃)在氮循环和空气污染中起着重要作用,因此追踪排放源并预测源贡献对于制定减轻土壤氨挥发环境危害的发展战略至关重要。氮自然丰度(δ¹⁵N)的测量可作为一种补充工具,用于分配排放源,以解决多个氨排放源对大气氨污染的贡献问题。然而,目前缺乏不同施氮量下整个挥发过程中δ¹⁵N-NH₃值变化的信息。因此,为填补这一空白,我们进行了为期15天的培养实验,包括不同尿素氮施用量,以确定挥发过程中NH₃的δ¹⁵N值。结果表明,挥发过程使NH₃中的氮减少。从0、20、180和360 kg N·ha⁻¹处理中挥发的NH₃的平均δ¹⁵N值分别为-16.2±7.3‰、-26.0±5.4‰、-34.8±4.8‰和-40.6±5.7‰。总体而言,在整个挥发过程中,δ¹⁵N-NH₃值范围为-46.0‰至-4.7‰,较高尿素氮施用量处理中的值低于对照处理。NH₃挥发过程中的δ¹⁵N-NH₃值远低于主要来源土壤(-3.4±0.1‰)和尿素(-3.6±0.1‰)的值。因此,土壤挥发过程中可能发生较大的同位素分馏。此外,本研究观察到土壤NH₄⁺-N与NH₃挥发速率和δ¹⁵N-NH₃值之间存在负相关关系。我们的结果可作为氨源分配和氮循环的证据。