Measurement Report: Long-term Assessment of Primary and Secondary Organic Aerosols in Shanghai Megacity throughout China’s Clean Air Actions since 2010

IF 5.2 1区 地球科学 Q1 ENVIRONMENTAL SCIENCES Atmospheric Chemistry and Physics Pub Date : 2024-06-24 DOI:10.5194/egusphere-2024-1488
Haifeng Yu, Yunhua Chang, Lin Cheng, Yusen Duan, Jianlin Hu
{"title":"Measurement Report: Long-term Assessment of Primary and Secondary Organic Aerosols in Shanghai Megacity throughout China’s Clean Air Actions since 2010","authors":"Haifeng Yu, Yunhua Chang, Lin Cheng, Yusen Duan, Jianlin Hu","doi":"10.5194/egusphere-2024-1488","DOIUrl":null,"url":null,"abstract":"<strong>Abstract.</strong> A growing body of research has demonstrated the effectiveness of China’s Air Pollution Prevention and Control Action Plan in controlling PM<sub>2.5</sub> pollution. However, there is a lack of long-term studies investigating the impact of these abatement policies on carbonaceous aerosols in PM<sub>2.5</sub>, particularly secondary organic carbon (SOC). Shanghai, as China’s largest megacity and prominent industrial hub, serves as a crucial gateway to the nation’s rapid development with a population exceeding twenty million. In this study, we conducted hourly online measurements of organic carbon (OC) and elemental carbon (EC) in PM<sub>2.5</sub> in Shanghai from July 2010 to July 2017. The results revealed that the annual concentrations (mean ± 1 σ) of OC and EC reached their peaks in 2013 (9.5 ± 6.4 and 2.7 ± 2.6 µg m<sup>-3</sup> to 3.0 ± 2.3 µg m<sup>-3</sup> and 2.7 ± 2.1 µg m<sup>-3</sup>). Subsequently, a consistent year-by-year decrease in both OC and EC concentrations was observed, mirroring the trend observed for PM<sub>2.5</sub>. Primary organic carbon (POC), the primary component of OC, accounted for an average of 65.6 %, displaying similar trends to OC. This finding indicates the effectiveness of primary emission control measures. However, the concentration of secondary organic carbon (SOC) did not decrease from 2013 to 2017, remaining relatively stable within the range of 2.7 ± 2.6 µg m<sup>-3</sup> to 3.0 ± 2.3 µg m<sup>-3</sup>. When considering data from previous studies in Shanghai, concentrations of SOC did not exhibit a noticeable decline until 2018, coinciding with the implementation of measures targeting volatile organic compounds (VOCs) emissions. Seasonally, with the exception of 2011, OC and EC concentrations were highest during winter, likely influenced by unfavourable meteorological conditions and long-range transport. SOC displayed no distinct seasonal fluctuations, as its formation is influenced by both photochemical reactions and meteorological conditions. POC and SOC exhibited different diurnal patterns, but neither showed a significant weekend effect, suggesting limited reduction in anthropogenic activities during weekends. Furthermore, SOC concentrations exhibited simultaneous increases in summer, particularly when O<sub>3</sub> concentrations exceeded 50 µg m<sup>-3</sup>, indicating that stronger oxidation reactions contribute to higher SOC concentrations. Our findings also revealed concentration gradients of SOC dependent on wind direction (WD) and wind speed (WS), with higher concentrations typically observed for winds originating from the southwest and northwest. Potential sources from distant regions were analyzed using the potential source contribution function (PSCF), indicating that the geographical potential source area is concentrated near the middle and lower Yangtze River.","PeriodicalId":8611,"journal":{"name":"Atmospheric Chemistry and Physics","volume":null,"pages":null},"PeriodicalIF":5.2000,"publicationDate":"2024-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Atmospheric Chemistry and Physics","FirstCategoryId":"89","ListUrlMain":"https://doi.org/10.5194/egusphere-2024-1488","RegionNum":1,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Abstract. A growing body of research has demonstrated the effectiveness of China’s Air Pollution Prevention and Control Action Plan in controlling PM2.5 pollution. However, there is a lack of long-term studies investigating the impact of these abatement policies on carbonaceous aerosols in PM2.5, particularly secondary organic carbon (SOC). Shanghai, as China’s largest megacity and prominent industrial hub, serves as a crucial gateway to the nation’s rapid development with a population exceeding twenty million. In this study, we conducted hourly online measurements of organic carbon (OC) and elemental carbon (EC) in PM2.5 in Shanghai from July 2010 to July 2017. The results revealed that the annual concentrations (mean ± 1 σ) of OC and EC reached their peaks in 2013 (9.5 ± 6.4 and 2.7 ± 2.6 µg m-3 to 3.0 ± 2.3 µg m-3 and 2.7 ± 2.1 µg m-3). Subsequently, a consistent year-by-year decrease in both OC and EC concentrations was observed, mirroring the trend observed for PM2.5. Primary organic carbon (POC), the primary component of OC, accounted for an average of 65.6 %, displaying similar trends to OC. This finding indicates the effectiveness of primary emission control measures. However, the concentration of secondary organic carbon (SOC) did not decrease from 2013 to 2017, remaining relatively stable within the range of 2.7 ± 2.6 µg m-3 to 3.0 ± 2.3 µg m-3. When considering data from previous studies in Shanghai, concentrations of SOC did not exhibit a noticeable decline until 2018, coinciding with the implementation of measures targeting volatile organic compounds (VOCs) emissions. Seasonally, with the exception of 2011, OC and EC concentrations were highest during winter, likely influenced by unfavourable meteorological conditions and long-range transport. SOC displayed no distinct seasonal fluctuations, as its formation is influenced by both photochemical reactions and meteorological conditions. POC and SOC exhibited different diurnal patterns, but neither showed a significant weekend effect, suggesting limited reduction in anthropogenic activities during weekends. Furthermore, SOC concentrations exhibited simultaneous increases in summer, particularly when O3 concentrations exceeded 50 µg m-3, indicating that stronger oxidation reactions contribute to higher SOC concentrations. Our findings also revealed concentration gradients of SOC dependent on wind direction (WD) and wind speed (WS), with higher concentrations typically observed for winds originating from the southwest and northwest. Potential sources from distant regions were analyzed using the potential source contribution function (PSCF), indicating that the geographical potential source area is concentrated near the middle and lower Yangtze River.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
测量报告:2010 年以来中国清洁空气行动期间上海特大城市一次和二次有机气溶胶的长期评估
摘要越来越多的研究表明,中国的《大气污染防治行动计划》在控制 PM2.5 污染方面卓有成效。然而,目前还缺乏有关这些减排政策对 PM2.5 中碳质气溶胶,尤其是二次有机碳 (SOC) 影响的长期研究。上海是中国最大的特大城市和著名的工业中心,人口超过两千万,是中国快速发展的重要门户。在本研究中,我们对 2010 年 7 月至 2017 年 7 月期间上海 PM2.5 中的有机碳(OC)和元素碳(EC)进行了每小时在线测量。结果显示,有机碳和元素碳的年浓度(平均值±1 σ)在2013年达到峰值(9.5±6.4和2.7±2.6 µg m-3至3.0±2.3 µg m-3和2.7±2.1 µg m-3)。随后,OC 和 EC 浓度逐年下降,与 PM2.5 的下降趋势一致。OC 的主要成分原始有机碳 (POC) 平均占 65.6%,其变化趋势与 OC 相似。这一结果表明了一次排放控制措施的有效性。然而,从2013年到2017年,二次有机碳(SOC)的浓度并没有下降,保持在2.7±2.6 µg m-3到3.0±2.3 µg m-3的范围内相对稳定。考虑到上海以往研究的数据,SOC 的浓度直到 2018 年才出现明显下降,与针对挥发性有机化合物(VOC)排放的措施的实施时间相吻合。从季节上看,除 2011 年外,OC 和 EC 的浓度在冬季最高,这可能是受到不利气象条件和长程飘移的影响。SOC 没有明显的季节性波动,因为其形成受到光化学反应和气象条件的影响。POC 和 SOC 表现出不同的昼夜变化规律,但都没有表现出明显的周末效应,这表明周末人为活动减少有限。此外,SOC 浓度在夏季同时增加,尤其是当 O3 浓度超过 50 µg m-3 时,这表明较强的氧化反应导致 SOC 浓度升高。我们的研究结果还显示,SOC 的浓度梯度取决于风向(WD)和风速(WS),通常西南风和西北风的浓度较高。利用潜在污染源贡献函数(PSCF)分析了来自遥远地区的潜在污染源,结果表明地理上的潜在污染源区域集中在长江中下游附近。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
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.
期刊最新文献
Interannual variations in Siberian carbon uptake and carbon release period Large contributions of soil emissions to the atmospheric nitrogen budget and their impacts on air quality and temperature rise in North China Critical contribution of chemically diverse carbonyl molecules to the oxidative potential of atmospheric aerosols Finite domains cause bias in measured and modeled distributions of cloud sizes Upper-atmosphere responses to the 2022 Hunga Tonga–Hunga Ha′apai volcanic eruption via acoustic gravity waves and air–sea interaction
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1