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中国南方农村地区二次有机气溶胶示踪物的季节性循环:大气氧化剂的重要性。

Seasonal cycles of secondary organic aerosol tracers in rural Guangzhou, Southern China: The importance of atmospheric oxidants.

机构信息

Guangdong Provincial Key Laboratory of Atmospheric Environment and Pollution Control, School of Environment and Energy, South China University of Technology, Guangzhou, China.

State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China.

出版信息

Environ Pollut. 2018 Sep;240:884-893. doi: 10.1016/j.envpol.2018.05.009. Epub 2018 May 26.

Abstract

Thirteen secondary organic aerosol (SOA) tracers of isoprene (SOA), monoterpenes (SOA), sesquiterpenes (SOA) and aromatics (SOA) in fine particulate matter (PM) were measured at a Pearl River Delta (PRD) regional site for one year. The characteristics including their seasonal cycles and the factors influencing their formation in this region were studied. The seasonal patterns of SOA, SOA and SOA tracers were characterized over three enhancement periods in summer (I), autumn (II) and winter (III), while the elevations of SOA tracer (i.e., 2,3-dihydroxy-4-oxopentanoic acid, DHOPA) were observed in Periods II and III. We found that SOA formed from different biogenic precursors could be driven by several factors during a one-year seasonal cycle. Isoprene emission controlled SOA formation throughout the year, while monoterpene and sesquiterpene emissions facilitated SOA and SOA formation in summer rather than in other seasons. The influence of atmospheric oxidants (O) was found to be an important factor of the formation of SOA tracers during the enhancement periods in autumn and winter. The formation of SOA tracer was influenced by the precursor emissions in summer, atmospheric oxidation in autumn and probably also by biomass burning in both summer and winter. In this study, we could not see the strong contribution of biomass burning to DHOPA as suggested by previous studies in this region. Instead, good correlations between observed DHOPA and O as well as [NO][O] suggest the involvement of both ozone (O) and nitrogen dioxide (NO) in the formation of DHOPA. The results showed that regional air pollution may not only increase the emissions of aromatic precursors but also can greatly promote the formation processes.

摘要

一年内,在珠江三角洲(PRD)地区站点测量了细颗粒物(PM)中 13 种异戊二烯(SOA)、单萜(SOA)、倍半萜(SOA)和芳烃(SOA)的二次有机气溶胶(SOA)示踪剂。研究了该地区这些示踪剂的形成特征及其季节性变化和影响因素。在夏季(I)、秋季(II)和冬季(III)三个增强期对 SOA、SOA 和 SOA 示踪剂的季节性模式进行了研究,而在 II 期和 III 期观察到了 SOA 示踪剂(即 2,3-二羟基-4-氧戊酸,DHOPA)的升高。我们发现,在一年的季节性周期中,不同生物源前体形成的 SOA 可能受到多种因素的驱动。异戊二烯排放控制着全年 SOA 的形成,而单萜烯和倍半萜烯排放则促进了夏季而不是其他季节 SOA 和 SOA 的形成。研究发现,大气氧化剂(O)的影响是秋季和冬季增强期 SOA 示踪剂形成的一个重要因素。夏季前体排放、秋季大气氧化以及夏季和冬季可能的生物质燃烧都对 SOA 示踪剂的形成产生了影响。在本研究中,我们没有像该地区之前的研究那样,看到生物质燃烧对 DHOPA 的强烈贡献。相反,观察到的 DHOPA 与 O 和 [NO][O] 之间的良好相关性表明,臭氧(O)和二氧化氮(NO)都参与了 DHOPA 的形成。研究结果表明,区域空气污染不仅会增加芳烃前体的排放,还会极大地促进其形成过程。

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