技术说明:完善当地 NOx 的 δ15N 同位素指纹,准确识别 PM2.5 中硝酸盐的来源

IF 5.2 1区 地球科学 Q1 ENVIRONMENTAL SCIENCES Atmospheric Chemistry and Physics Pub Date : 2024-06-27 DOI:10.5194/egusphere-2024-1621
Hao Xiao, Qinkai Li, Shiyuan Ding, Wenjing Dai, Gaoyang Cui, Xiaodong Li
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摘要

摘要稳定氮同位素组成(δ15N)已被证明是识别 PM2.5 中硝酸盐(NO3-)来源的重要工具。然而,由于缺乏对国内氮氧化物来源的δ15N值的系统研究,阻碍了对中国氮氧化物来源的准确识别。在此,我们采用主动采样方法,系统测定并完善了天津地区六类氮氧化物源的δ15N值。此外,在天津污染最严重的采暖前期、采暖中期和采暖后期,测定了 PM2.5 中 NO3- 的 δ15N 值。结果表明,天津市六类氮氧化物源的同位素指纹具有代表性和区域性特征。贝叶斯同位素混合(MixSIAR)模型表明,燃煤、生物质燃烧和汽车尾气的总贡献率超过 60%,是天津采样时段 NO3- 的主要来源。但是,如果不考虑当地氮氧化物来源的同位素特征,可能会导致低估燃煤的贡献。此外,工业源是以往研究中未定性的来源,它的缺失可能直接导致模型高估其他来源的贡献率超过 15%。值得注意的是,随着输入到模型中的污染源数量的增加,各种氮氧化物污染源的贡献率变得越来越稳定,各种污染源之间的相互影响也显著降低。这项研究表明,针对特定区域的精细同位素指纹能更有效地区分 NO3-的来源,从而为控制 NO3-污染提供有价值的见解。
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Technical note: Refining δ15N isotopic fingerprints of local NOx for accurate source identification of nitrate in PM2.5
Abstract. Stable nitrogen isotopic composition (δ15N) has proven to be a valuable tool for identifying sources of nitrates (NO3) in PM2.5. However, the absence of a systematic study on the δ15N values of domestic NOx sources hinders accurate identification of NO3 sources in China. Here, we systematically determined and refined δ15N values for six categories of NOx sources in the local Tianjin area using an active sampling method. Moreover, the δ15N values of NO3 in PM2.5 were measured during pre-heating, mid-heating and late-heating periods, which are the most heavily polluted in Tianjin. Results shown that the representative nature and region-specific characteristics of isotopic fingerprints for six categories of NOx sources in Tianjin. The Bayesian isotope mixing (MixSIAR) model demonstrated that coal combustion, biomass burning, and vehicle exhaust collectively contributed more than 60 %, dominating the sources of NO3 during sampling periods in Tianjin. However, failure to consider the isotopic signatures of local NOx sources could result in an underestimation of the contribution from coal combustion. Additionally, the absence of industrial sources, an uncharacterized source in previous studies, may directly result in the contribution fraction of other sources being overestimated by the model more than 15 %. Notably, as the number of sources input to the model increased, the contribution of various NOx sources was becoming more stable, and the inter-influence between various sources significantly reduced. This study demonstrated that the refined isotopic fingerprint in a region-specific context could more effectively distinguish source of NO3, thereby providing valuable insights for controlling NO3 pollution.
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来源期刊
Atmospheric Chemistry and Physics
Atmospheric Chemistry and Physics 地学-气象与大气科学
CiteScore
10.70
自引率
20.60%
发文量
702
审稿时长
6 months
期刊介绍: Atmospheric Chemistry and Physics (ACP) is a not-for-profit international scientific journal dedicated to the publication and public discussion of high-quality studies investigating the Earth''s atmosphere and the underlying chemical and physical processes. It covers the altitude range from the land and ocean surface up to the turbopause, including the troposphere, stratosphere, and mesosphere. The main subject areas comprise atmospheric modelling, field measurements, remote sensing, and laboratory studies of gases, aerosols, clouds and precipitation, isotopes, radiation, dynamics, biosphere interactions, and hydrosphere interactions. The journal scope is focused on studies with general implications for atmospheric science rather than investigations that are primarily of local or technical interest.
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