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Measurement report: Hydrolyzed amino acids in fine and coarse atmospheric aerosol in Nanchang, China: concentrations, compositions, sources and possible bacterial degradation state

机译:测量报告:中国南昌的细粗大气气溶胶中水解氨基酸:浓度,组成,来源和可能的细菌降解状态

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Amino acids (AAs) are relevant for nitrogen cycles, climate change and public health. Their size distribution may help to uncover the source, transformation and fate of protein in the atmosphere. This paper explores the use of compound-specific δ 15 N patterns of hydrolyzed amino acid (HAA), δ 15 N values of total hydrolyzed amino acid ( δ 15 N THAA ), degradation index (DI) and the variance within trophic AAs ( ∑ V ) as markers to examine the sources and processing history of different sizes of particle in the atmosphere. Two weeks of daily aerosol samples from five sampling sites in the Nanchang area (Jiangxi Province, China) and samples of main emission sources of AAs in aerosols (biomass burning, soil and plants) were collected (Zhu et al., 2020). Here, we measured the concentrations and δ 15 N values of each HAA in two size-segregated aerosol particles ( ?2.5? μ m and PM 2.5 ). Our results showed that the average concentrations of THAA in fine particles was nearly 6 times higher than that in coarse particles ( p ? ?0.01) and composition profiles of fine and coarse particles were quite different from each other. The δ 15 N values of hydrolyzed glycine and THAA in both fine and coarse particles were typically in the range of those from biomass burning, soil and plant sources. Moreover, the average difference in the δ 15 N THAA value between fine and coarse particles was smaller than 1.5?‰. These results suggested that the sources of atmospheric HAAs for fine and coarse particles might be similar. Meanwhile, compared to fine particles, significantly lower DI values ( p ? ? ? ?0.05), “scattered” δ 15 N distribution in trophic AA and higher ∑ V values ( p ? ?0.05) were observed in coarse particles. But the difference in δ 15 N values of source AA (glycine, serine, phenylalanine and lysine) and THAA between coarse particles and fine particles was relatively small. It is likely that AAs in coarse particles have advanced bacterial degradation states compared to fine particles. Besides that, the significant increase in DI values and a decrease in ∑ V values for coarse particles were observed on days on which precipitation fell ( p ? ? ? ?0.05). This implies that “fresh” AAs in coarse particles were likely released following the precipitation.
机译:氨基酸(AAS)与氮循环,气候变化和公共卫生有关。它们的大小分布可能有助于在大气中揭示蛋白质的源极,转化和命运。本文探讨了使用总水解氨基酸(HAA)的化合物特异性δ15n模式,总水解氨基酸(δ15nAA),降解指数(di)和营养AAS内的方差(σ v)作为标记,以检查大气中不同尺寸的粒子的来源和处理历史。收集了南昌地区(江西省,中国)的五个抽样场地的每日烟雾样本的两周时间(江西省)和气溶胶中AAS的主要排放来源(生物量燃烧,土壤和植物)(Zhu等,2020)。这里,我们测量了两个尺寸隔离的气溶胶颗粒中每个HAA的浓度和δ15n值(&β2.5?μm和pm 2.5)。我们的研究结果表明,细颗粒中ThAA的平均浓度比粗颗粒的平均浓度高(P?0.1),并且细小颗粒的组成谱彼此完全不同。在细小和粗颗粒中的水解甘氨酸和ThAA的δ15n值通常在生物质燃烧,土壤和植物来源的范围内。此外,细小颗粒之间的δ15nthaa值的平均差异小于1.5≤1。这些结果表明,用于精细和粗颗粒的大气HAAs来源可能是相似的。同时,与细颗粒相比,在粗颗粒中观察到促进AA中的“散射”Δ15n分布,“散射”δ15n分布在粗颗粒中观察到较高的颗粒,“散射”δ15n。但是粗颗粒和细颗粒之间的施源AA(甘氨酸,丝氨酸,苯丙氨酸和赖氨酸)和ThaA的δ15n值的差异相对较小。与细颗粒​​相比,粗颗粒中的AA均具有晚期细菌降解状态。除此之外,在降水下降的天数下观察到DI值的显着增加和σV值的σV值(p ????0.05)。这意味着在沉淀后可能释放出粗颗粒中的“新鲜”AAS。

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