Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/61934
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dc.contributorDepartment of Civil and Environmental Engineering-
dc.creatorLing, ZH-
dc.creatorGuo, H-
dc.creatorSimpson, IJ-
dc.creatorSaunders, SM-
dc.creatorLam, SHM-
dc.creatorLyu, XP-
dc.creatorBlake, DR-
dc.date.accessioned2016-12-19T08:57:51Z-
dc.date.available2016-12-19T08:57:51Z-
dc.identifier.issn1680-7316en_US
dc.identifier.urihttp://hdl.handle.net/10397/61934-
dc.language.isoenen_US
dc.publisherCopernicus GmbHen_US
dc.rights© Author(s) 2016. This is an open access article distributed under the Creative Commons Attribution 3.0 License (https://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following publication: Ling, Z., Guo, H., Simpson, I. J., Saunders, S. M., Lam, S. H. M., Lyu, X., and Blake, D. R.: New insight into the spatiotemporal variability and source apportionments of C1–C4 alkyl nitrates in Hong Kong, Atmos. Chem. Phys., 16, 8141-8156 is available at https://doi.org/10.5194/acp-16-8141-2016, 2016.en_US
dc.titleNew insight into the spatiotemporal variability and source apportionments of C1-C4 alkyl nitrates in Hong Kongen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage8141en_US
dc.identifier.epage8156en_US
dc.identifier.volume16en_US
dc.identifier.issue13en_US
dc.identifier.doi10.5194/acp-16-8141-2016en_US
dcterms.abstractC1-C4 alkyl nitrates (RONO2/were measured concurrently at a mountain site, Tai Mo Shan (TMS), and an urban site, Tsuen Wan (TW), at the base of the same mountain in Hong Kong from September to November 2010. Although the levels of parent hydrocarbons were much lower at TMS (p <0.05), similar alkyl nitrate levels were found at both sites regardless of the elevation difference, suggesting various source contributions of alkyl nitrates at the two sites. Prior to using a positive matrix factorization (PMF) model, the data at TW were divided into "meso" and "non-meso" scenarios for the investigation of source apportionments with the influence of mesoscale circulation and regional transport, respectively. Secondary formation was the prominent contributor of alkyl nitrates in the meso scenario (60±2 %, 60.2±1.2 pptv), followed by biomass burning and oceanic emissions, while biomass burning and secondary formation made comparable contributions to alkyl nitrates in the nonmeso scenario, highlighting the strong emissions of biomass burning in the inland Pearl River delta (PRD) region. In contrast to TW, the alkyl nitrate levels measured at TMS mainly resulted from the photooxidation of the parent hydrocarbons at TW during mesoscale circulation, i.e., valley breezes, corresponding to 52-86% of the alkyl nitrate levels at TMS. Furthermore, regional transport from the inland PRD region made significant contributions to the levels of alkyl nitrates (∼58-82 %) at TMS in the non-meso scenario, resulting in similar levels of alkyl nitrates observed at the two sites. The simulation of secondary formation pathways using a photochemical box model found that the reaction of alkyl peroxy radicals (RO2/with nitric oxide (NO) dominated the formation of RONO2 at both sites, and the formation of alkyl nitrates contributed negatively to O3 production, with average reduction rates of 4.1 and 4.7 pptv pptv-1 at TMS and TW, respectively.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAtmospheric chemistry and physics, 2016, v. 16, no. 13, p. 8141-8156-
dcterms.isPartOfAtmospheric chemistry and physics-
dcterms.issued2016-
dc.identifier.isiWOS:000381091400006-
dc.identifier.scopus2-s2.0-84978159497-
dc.identifier.ros2016001881-
dc.identifier.eissn1680-7324en_US
dc.identifier.rosgroupid2016001845-
dc.description.ros2016-2017 > Academic research: refereed > Publication in refereed journalen_US
dc.description.validate201811_a bcmaen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberRGC-B1-075, OA_IR/PIRAen_US
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
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