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dc.contributor.authorLi, Guohui
dc.contributor.authorMolina, Luisa Tan
dc.contributor.authorBei, Naifang
dc.contributor.authorTie, Xuexi
dc.date.accessioned2011-10-20T17:28:11Z
dc.date.available2011-10-20T17:28:11Z
dc.date.issued2011-06
dc.date.submitted2011-05
dc.identifier.issn1680-7324
dc.identifier.issn1680-7316
dc.identifier.urihttp://hdl.handle.net/1721.1/66523
dc.description.abstractIn the present study, the impact of aerosols on the photochemistry in Mexico City is evaluated using the WRF-CHEM model for the period from 24 to 29 March during the MCMA-2006/MILAGRO campaign. An aerosol radiative module has been developed with detailed consideration of aerosol size, composition, and mixing. The module has been coupled into the WRF-CHEM model to calculate the aerosol optical properties, including optical depth, single scattering albedo, and asymmetry factor. Calculated aerosol optical properties are in good agreement with the surface observations and aircraft and satellite measurements during daytime. In general, the photolysis rates are reduced due to the absorption by carbonaceous aerosols, particularly in the early morning and late afternoon hours with a long aerosol optical path. However, with the growth of aerosol particles and the decrease of the solar zenith angle around noontime, aerosols can slightly enhance photolysis rates when ultraviolet (UV) radiation scattering dominates UV absorption by aerosols at the lower-most model layer. The changes in photolysis rates due to aerosols lead to about 2–17 % surface ozone reduction during daytime in the urban area in Mexico City with generally larger reductions during early morning hours near the city center, resulting in a decrease of OH level by about 9 %, as well as a decrease in the daytime concentrations of nitrate and secondary organic aerosols by 5–6 % on average. In addition, the rapid aging of black carbon aerosols and the enhanced absorption of UV radiation by organic aerosols contribute substantially to the reduction of photolysis rates.en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Atmospheric Chemistry Program (ATM-0528227)en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Atmospheric Chemistry Program (ATM-0810931)en_US
dc.description.sponsorshipMolina Center for Energy and the Environmenten_US
dc.language.isoen_US
dc.publisherEuropean Geosciences Unionen_US
dc.relation.isversionofhttp://dx.doi.org/10.5194/acp-11-5169-2011en_US
dc.rightsCreative Commons Attribution 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/en_US
dc.sourceCopernicusen_US
dc.titleAerosol effects on the photochemistry in Mexico City during MCMA-2006/MILAGRO campaignen_US
dc.typeArticleen_US
dc.identifier.citationLi, G. et al. “Aerosol effects on the photochemistry in Mexico City during MCMA-2006/MILAGRO campaign.” Atmospheric Chemistry and Physics 11 (2011): 5169-5182. Web. 20 Oct. 2011.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciencesen_US
dc.contributor.approverMolina, Luisa Tan
dc.contributor.mitauthorLi, Guohui
dc.contributor.mitauthorMolina, Luisa Tan
dc.relation.journalAtmospheric Chemistry and Physicsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsLi, G.; Bei, N.; Tie, X.; Molina, L. T.en
dc.identifier.orcidhttps://orcid.org/0000-0002-3596-5334
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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