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Significant chlorine emissions from biomass burning affect the long-term atmospheric chemistry in Asia

MPS-Authors
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Chang,  Di
Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Dai,  Jianing
Department of Civil and Environmental Engineering, The Hong Kong Polytechnic University, Hong Kong;
Environmental Modelling, MPI for Meteorology, Max Planck Society;

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Brasseur,  Guy P.       
Department of Civil and Environmental Engineering, The Hong Kong Polytechnic University, Hong Kong;
Environmental Modelling, MPI for Meteorology, Max Planck Society;
Atmospheric Chemistry Observation & Modeling Laboratory, National Center for Atmospheric Research, Boulder, USA ;

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Pozzer,  Andrea
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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nwae285.pdf
(Publisher version), 2MB

Supplementary Material (public)

nwae285_supplemental_file.pdf
(Supplementary material), 12MB

Citation

Chang, D., Li, Q., Wang, Z., Dai, J., Fu, X., Guo, J., et al. (2024). Significant chlorine emissions from biomass burning affect the long-term atmospheric chemistry in Asia. National Science Review, 11: nwae285. doi:10.1093/nsr/nwae285.


Cite as: https://hdl.handle.net/21.11116/0000-000F-F01D-2
Abstract
Biomass burning (BB) is a major source of trace gases and particles to the atmosphere, influencing air quality, radiative balance, and climate. Previous studies have mostly focused on the BB emissions of carbon and nitrogen species with less attention on chlorine. Reactive chlorine chemistry has significant effects on atmospheric chemistry and air quality. However, quantitative information on chlorine emissions from BB, particularly the long-term trend and associated atmospheric impacts, is limited both on regional and global scales. Here, we report a long-term (2001–2018) high-resolution BB emission inventory for the major chlorine-containing compounds (HCl, chloride, and CH3Cl) in Asia based on satellite observations. We estimate an average of 177 Gg yr−1 chlorine emitted from BB activity in Asia, with the BB-to-anthropogenic ratio ranging from approximately 1:5 to 1:7 in this region. Distinct seasonal patterns and significant spatial and interannual variability are observed, mainly driven by human-mediated changes in agricultural activities. By incorporating the newly developed chlorine emission inventory into a global chemistry-climate model (CAM-Chem), we find that the BB-chlorine emissions lead to elevated levels of HCl and CH3Cl (monthly average up to 2062 and 1421 parts per trillion by volume (pptv), respectively), subsequently resulting in noticeable changes in oxidants (up to 3.1% in O3 and 17% in OH radicals). The results demonstrate that BB is not only a significant source of air pollutants but also of oxidants, suggesting a larger role of BB emissions in the atmospheric chemistry and oxidation process than previously appreciated. In light of the projected increasing BB activity toward the end of the century and the extensive control of anthropogenic emissions worldwide, the contribution of BB emissions may become fundamental to air quality composition in the future.