Articles | Volume 22, issue 11
https://doi.org/10.5194/acp-22-7827-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-22-7827-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Measurement report: Effects of anthropogenic emissions and environmental factors on the formation of biogenic secondary organic aerosol (BSOA) in a coastal city of southeastern China
Youwei Hong
CORRESPONDING AUTHOR
Center for Excellence in Regional Atmospheric Environment, Institute
of Urban Environment, Chinese Academy of Sciences, Xiamen, 361021, China
Key Lab of Urban Environment and Health, Institute of Urban
Environment, Chinese Academy of Sciences, Xiamen, 361021, China
University of Chinese Academy of Sciences, Beijing, 100049, China
School of Life Sciences, Hebei University, Baoding, 071000, China
Xinbei Xu
Center for Excellence in Regional Atmospheric Environment, Institute
of Urban Environment, Chinese Academy of Sciences, Xiamen, 361021, China
Key Lab of Urban Environment and Health, Institute of Urban
Environment, Chinese Academy of Sciences, Xiamen, 361021, China
University of Chinese Academy of Sciences, Beijing, 100049, China
Dan Liao
College of Environment and Public Health, Xiamen Huaxia University,
Xiamen 361024, China
Taotao Liu
Center for Excellence in Regional Atmospheric Environment, Institute
of Urban Environment, Chinese Academy of Sciences, Xiamen, 361021, China
Key Lab of Urban Environment and Health, Institute of Urban
Environment, Chinese Academy of Sciences, Xiamen, 361021, China
University of Chinese Academy of Sciences, Beijing, 100049, China
Xiaoting Ji
Center for Excellence in Regional Atmospheric Environment, Institute
of Urban Environment, Chinese Academy of Sciences, Xiamen, 361021, China
Key Lab of Urban Environment and Health, Institute of Urban
Environment, Chinese Academy of Sciences, Xiamen, 361021, China
University of Chinese Academy of Sciences, Beijing, 100049, China
Ke Xu
Center for Excellence in Regional Atmospheric Environment, Institute
of Urban Environment, Chinese Academy of Sciences, Xiamen, 361021, China
Key Lab of Urban Environment and Health, Institute of Urban
Environment, Chinese Academy of Sciences, Xiamen, 361021, China
School of Life Sciences, Hebei University, Baoding, 071000, China
Chunyang Liao
State Key Laboratory of Environmental Chemistry and Ecotoxicology,
Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences,
Beijing 100085, China
Ting Wang
Institute of Earth Environment, Chinese Academy of Sciences, Xi'an,
710061, China
Chunshui Lin
Institute of Earth Environment, Chinese Academy of Sciences, Xi'an,
710061, China
Center for Excellence in Regional Atmospheric Environment, Institute
of Urban Environment, Chinese Academy of Sciences, Xiamen, 361021, China
Key Lab of Urban Environment and Health, Institute of Urban
Environment, Chinese Academy of Sciences, Xiamen, 361021, China
University of Chinese Academy of Sciences, Beijing, 100049, China
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Jing Duan, Ru-Jin Huang, Yifang Gu, Chunshui Lin, Haobin Zhong, Wei Xu, Quan Liu, Yan You, Jurgita Ovadnevaite, Darius Ceburnis, Thorsten Hoffmann, and Colin O'Dowd
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Haobin Zhong, Ru-Jin Huang, Chunshui Lin, Wei Xu, Jing Duan, Yifang Gu, Wei Huang, Haiyan Ni, Chongshu Zhu, Yan You, Yunfei Wu, Renjian Zhang, Jurgita Ovadnevaite, Darius Ceburnis, and Colin D. O'Dowd
Atmos. Chem. Phys., 22, 9513–9524, https://doi.org/10.5194/acp-22-9513-2022, https://doi.org/10.5194/acp-22-9513-2022, 2022
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To investigate the physico-chemical properties of aerosol transported from major pollution regions in China, observations were conducted ~200 m above the ground at the junction location of the two key pollution areas. We found that the formation efficiency, oxidation state and production rate of secondary aerosol were different in the transport sectors from different pollution regions, and they were largely enhanced by the regional long-distance transport.
Taotao Liu, Yiling Lin, Jinsheng Chen, Gaojie Chen, Chen Yang, Lingling Xu, Mengren Li, Xiaolong Fan, Yanting Chen, Liqian Yin, Yuping Chen, Xiaoting Ji, Ziyi Lin, Fuwang Zhang, Hong Wang, and Youwei Hong
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2022-292, https://doi.org/10.5194/acp-2022-292, 2022
Revised manuscript not accepted
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Field observations and models analysis were carried out in a coastal city to study HCHO formation mechanism and its impacts on photochemistry. HCHO contributed to atmospheric oxidation by around 10 %, reflecting its significance in photochemistry. Disabling HCHO mechanism made net O3 production rates decrease by 31 %, which were dominated by the reductions of pathways relating to radical reactions, indicating the HCHO affected O3 mainly by controlling the efficiencies of radical propagation.
Taotao Liu, Gaojie Chen, Jinsheng Chen, Lingling Xu, Mengren Li, Youwei Hong, Yanting Chen, Xiaoting Ji, Chen Yang, Yuping Chen, Weiguo Huang, Quanjia Huang, and Hong Wang
Atmos. Chem. Phys., 22, 4339–4353, https://doi.org/10.5194/acp-22-4339-2022, https://doi.org/10.5194/acp-22-4339-2022, 2022
Short summary
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We clarified the seasonal variations of PAN pollution, influencing factors, its mechanisms, and impacts on O3 based on OBM and GAM models. PAN presented inhibition and promotion effects on O3 under low and high ROx levels. Monitoring of PAN and its precursors, and the quantification of its impacts on O3 formation, significantly guide photochemical pollution control. The analysis methods used in this study provide a reference for study of the formation mechanisms of PAN and O3 in other regions.
Taotao Liu, Youwei Hong, Mengren Li, Lingling Xu, Jinsheng Chen, Yahui Bian, Chen Yang, Yangbin Dan, Yingnan Zhang, Likun Xue, Min Zhao, Zhi Huang, and Hong Wang
Atmos. Chem. Phys., 22, 2173–2190, https://doi.org/10.5194/acp-22-2173-2022, https://doi.org/10.5194/acp-22-2173-2022, 2022
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Based on the OBM-MCM model analyses, the study aims to clarify (1) the pollution characteristics of O3 and its precursors, (2) the atmospheric oxidation capacity and radical chemistry, and (3) the O3 formation mechanism and sensitivity analysis. The results are expected to enhance the understanding of the O3 formation mechanism with low O3 precursor levels and provide scientific evidence for O3 pollution control in coastal cities.
Baoye Hu, Jun Duan, Youwei Hong, Lingling Xu, Mengren Li, Yahui Bian, Min Qin, Wu Fang, Pinhua Xie, and Jinsheng Chen
Atmos. Chem. Phys., 22, 371–393, https://doi.org/10.5194/acp-22-371-2022, https://doi.org/10.5194/acp-22-371-2022, 2022
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There has been a lack of research into HONO in coastal cities with low concentrations of PM2.5, but strong sunlight and high humidity. Insufficient research on coastal cities with good air quality has resulted in certain obstacles to assessing the photochemical processes in these areas. Furthermore, HONO contributes to the atmospheric photochemistry depending on the season. Therefore, observations of HONO across four seasons in the southeastern coastal area of China are urgently needed.
Lingling Xu, Jiayan Shi, Yuping Chen, Yanru Zhang, Mengrong Yang, Yanting Chen, Liqian Yin, Lei Tong, Hang Xiao, and Jinsheng Chen
Atmos. Chem. Phys., 21, 18543–18555, https://doi.org/10.5194/acp-21-18543-2021, https://doi.org/10.5194/acp-21-18543-2021, 2021
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Mercury (Hg) isotopic compositions in aerosols are the mixed results of emission sources and atmospheric processes. This study presents Hg isotopic compositions in PM2.5 from different types of locations and total Hg from offshore surface seawater. The results indicate that atmospheric transformations induce significant mass independent fractionation of Hg isotopes, which obscures Hg isotopic signatures of initial emissions.
Chunshui Lin, Darius Ceburnis, Anna Trubetskaya, Wei Xu, William Smith, Stig Hellebust, John Wenger, Colin O'Dowd, and Jurgita Ovadnevaite
Atmos. Meas. Tech., 14, 6905–6916, https://doi.org/10.5194/amt-14-6905-2021, https://doi.org/10.5194/amt-14-6905-2021, 2021
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Source apportionment of solid-fuel-burning emissions can be complicated by the use of different fuels, stoves, and burning conditions. Here, the organic aerosol mass spectra produced from burning a range of solid fuels in several stoves were compared. This study accounts for the source variability and provides better constraints on the primary factor contributions to the ambient organic aerosol estimations, holding significant implications for public health and policymakers.
Wei Xu, Kirsten N. Fossum, Jurgita Ovadnevaite, Chunshui Lin, Ru-Jin Huang, Colin O'Dowd, and Darius Ceburnis
Atmos. Chem. Phys., 21, 8655–8675, https://doi.org/10.5194/acp-21-8655-2021, https://doi.org/10.5194/acp-21-8655-2021, 2021
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Cloud condensation nuclei (CCN) are an important topic in atmospheric studies, especially for evaluating the climate impact of aerosol. Here in this study, CCN closure is studied by using chemical composition based on an aerosol mass spectrometer (AMS) and hygroscopicity growth measurements based on a humidified tandem differential mobility analyzer (HTDMA) at the Mace Head atmospheric research station.
Wei Yuan, Ru-Jin Huang, Lu Yang, Ting Wang, Jing Duan, Jie Guo, Haiyan Ni, Yang Chen, Qi Chen, Yongjie Li, Ulrike Dusek, Colin O'Dowd, and Thorsten Hoffmann
Atmos. Chem. Phys., 21, 3685–3697, https://doi.org/10.5194/acp-21-3685-2021, https://doi.org/10.5194/acp-21-3685-2021, 2021
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We characterized the seasonal variations in nitrated aromatic compounds (NACs) in composition, sources, and their light absorption contribution to brown carbon (BrC) aerosol in Xi'an, Northwest China. Our results show that secondary formation and vehicular emission were dominant sources in summer (~80 %), and biomass burning and coal combustion were major sources in winter (~75 %), and they indicate that the composition and sources of NACs have a profound impact on the light absorption of BrC
Chunshui Lin, Darius Ceburnis, Wei Xu, Eimear Heffernan, Stig Hellebust, John Gallagher, Ru-Jin Huang, Colin O'Dowd, and Jurgita Ovadnevaite
Atmos. Chem. Phys., 20, 10513–10529, https://doi.org/10.5194/acp-20-10513-2020, https://doi.org/10.5194/acp-20-10513-2020, 2020
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Chemical composition and sources of submicron aerosols (PM1) were simultaneously investigated at a kerbside site in the Dublin city center and at a residential site in suburban Dublin (~5 km apart) during both a nonheating and a heating period in 2018. This study highlights the temporal and spatial variability of sources within the Dublin city center and the need for additional aerosol characterization studies to improve targeted mitigation solutions for a greater impact on urban air quality.
Baoye Hu, Jun Duan, Youwei Hong, Lingling Xu, Mengren Li, Yahui Bian, Min Qin, Wu Fang, Pinhua Xie, and Jinsheng Chen
Atmos. Chem. Phys. Discuss., https://doi.org/10.5194/acp-2020-880, https://doi.org/10.5194/acp-2020-880, 2020
Revised manuscript not accepted
Short summary
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There has been a lack of research into HONO in coastal cities with low concentrations of NOx and PM2.5, but strong sunlight and high humidity. Insufficient research on coastal cities with good air quality has resulted in certain obstacles to assessing the photochemical processes in these areas. Furthermore, HONO contributes to the atmospheric photochemistry depending on the season. Therefore, observations of HONO across four seasons in the southeastern coastal area of China are urgently needed.
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Short summary
Secondary organic aerosol (SOA) simulation remains uncertain, due to the unknown SOA formation mechanisms. Aerosol samples with a 4 h time resolution were collected, along with online measurements of aerosol chemical compositions and meteorological parameters. We found that anthropogenic emissions, atmospheric oxidation capacity and halogen chemistry have significant effects on the formation of biogenic SOA (BSOA). The findings of this study are helpful to better explore the missed SOA sources.
Secondary organic aerosol (SOA) simulation remains uncertain, due to the unknown SOA formation...
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