Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/107428
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dc.contributorDepartment of Civil and Environmental Engineeringen_US
dc.creatorLi, Hen_US
dc.creatorLyu, Xen_US
dc.creatorXue, Len_US
dc.creatorHuo, Yen_US
dc.creatorYao, Den_US
dc.creatorLu, Hen_US
dc.creatorGuo, Hen_US
dc.date.accessioned2024-06-21T06:11:52Z-
dc.date.available2024-06-21T06:11:52Z-
dc.identifier.issn1680-7316en_US
dc.identifier.urihttp://hdl.handle.net/10397/107428-
dc.language.isoenen_US
dc.publisherCopernicus GmbHen_US
dc.rights© Author(s) 2024. This work is distributed under the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Li, H., Lyu, X., Xue, L., Huo, Y., Yao, D., Lu, H., and Guo, H.: In situ measurement of organic aerosol molecular markers in urban Hong Kong during a summer period: temporal variations and source apportionment, Atmos. Chem. Phys., 24, 7085–7100 is available at https://doi.org/10.5194/acp-24-7085-2024, 2024.en_US
dc.titleIn situ measurement of organic aerosol molecular markers in urban Hong Kong during a summer period : temporal variations and source apportionmenten_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage7085en_US
dc.identifier.epage7100en_US
dc.identifier.volume24en_US
dc.identifier.issue12en_US
dc.identifier.doi10.5194/acp-24-7085-2024en_US
dcterms.abstractOrganic aerosol (OA) is a significant constituent of urban particulate matter (PM), and molecular markers therein provide information on the sources and formation mechanisms. With the in situ measurement of over 70 OA molecular markers in a summer month at a bihourly resolution, this study focused on the temporal variations in representative markers and dynamic source contributions to OA at an urban site in Hong Kong SAR (HK). The levels of secondary OA (SOA) markers were markedly elevated (p < 0.05) in the short-duration cases with continental and coastal air relative to those in the most common marine air, and the primary markers primarily contained local characteristics. The troughs showed the enhancements of many SOA markers (p < 0.05), which appeared to be related to the high relative humidity. The diurnal patterns of 2-methyltetrols varied in differed cases, and their aqueous formation at night seemed plausible, particularly in the presence of troughs. Eight sources were identified for the organic matter in submicron PM (PM1-OM). Despite being an urban site, the mean SOA contribution (66.1 ± 10.5 %), primarily anthropogenic, was significant. Anthropogenic SOA dominated in the cases with continental and coastal air and in the early afternoon. Local cooking and vehicle emissions became predominant in the case of marine air without troughs. Even averaged over the study period in this summer month with the prevalence of marine air, primary cooking emissions contributed up to 44.2 % to PM1-OM in the early evening. The study highlighted the need to control regional anthropogenic SOA and local cooking emissions to mitigate PM pollution in HK.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAtmospheric chemistry and physics, 2024, v. 24, no. 12, p. 7085-7100en_US
dcterms.isPartOfAtmospheric chemistry and physicsen_US
dcterms.issued2024-
dc.identifier.eissn1680-7324en_US
dc.description.validate202406 bcchen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera2868-n01-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Hong Kong Baptist University; Research Institute for Land and Space of the Hong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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