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dc.contributor.authorDusanter, S.
dc.contributor.authorVimal, D.
dc.contributor.authorStevens, P. S.
dc.contributor.authorVolkamer, R.
dc.contributor.authorMolina, Luisa Tan
dc.contributor.authorBaker, A.
dc.contributor.authorMeinardi, S.
dc.contributor.authorBlake, D.
dc.contributor.authorMerten, A.
dc.contributor.authorZhang, R.
dc.contributor.authorZheng, J.
dc.contributor.authorFortner, E. C.
dc.contributor.authorJunkermann, W.
dc.contributor.authorDubey, Madan
dc.contributor.authorRahn, T.
dc.contributor.authorEichinger, B.
dc.contributor.authorLewandowski, P.
dc.contributor.authorPrueger, J.
dc.contributor.authorHolder, H.
dc.contributor.authorSheehy, P. M.
dc.date.accessioned2012-01-03T20:55:05Z
dc.date.available2012-01-03T20:55:05Z
dc.date.issued2009-09
dc.date.submitted2009-08
dc.identifier.issn1680-7324
dc.identifier.issn1680-7316
dc.identifier.urihttp://hdl.handle.net/1721.1/67896
dc.description.abstractMeasurements of hydroxyl (OH) and hydroperoxy (HO2) radicals were made during the Mexico City Metropolitan Area (MCMA) field campaign as part of the MILAGRO (Megacity Initiative: Local and Global Research Observations) project during March 2006. These measurements provide a unique opportunity to test current models of atmospheric ROx (OH + HO2 + RO2) photochemistry under polluted conditions. A zero-dimensional box model based on the Regional Atmospheric Chemical Mechanism (RACM) was constrained by 10-min averages of 24 J-values and the concentrations of 97 chemical species. Several issues related to the ROx chemistry under polluted conditions are highlighted in this study: (i) Measured concentrations of both OH and HO2 were underpredicted during morning hours on a median campaign basis, suggesting a significant source of radicals is missing from current atmospheric models under polluted conditions, consistent with previous urban field campaigns. (ii) The model-predicted HO2/OH ratios underestimate the measurements for NO mixing ratios higher than 5 ppb, also consistent with previous urban field campaigns. This suggests that under high NOx conditions, the HO2 to OH propagation rate may be overestimated by the model or a process converting OH into HO2 may be missing from the chemical mechanism. On a daily basis (08:40 a.m.–06:40 p.m.), an analysis of the radical budget indicates that HONO photolysis, HCHO photolysis, O3-alkene reactions and dicarbonyls photolysis are the main radical sources. O3 photolysis contributes to less than 6% of the total radical production.en_US
dc.description.sponsorshipHenry & Camille Dreyfus Foundationen_US
dc.description.sponsorshipNational Science Foundation (U.S.) (ATM-9984152)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (0612738)en_US
dc.language.isoen_US
dc.publisherCopernicus Publications on behalf of the European Geosciences Unionen_US
dc.relation.isversionofhttp://dx.doi.org/10.5194/acp-9-6655-2009en_US
dc.rightsCreative Commons Attribution 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by/3.0en_US
dc.sourceCopernicusen_US
dc.titleMeasurements of OH and HO2 concentrations during the MCMA-2006 field campaign – Part 2: Model comparison and radical budgeten_US
dc.typeArticleen_US
dc.identifier.citationDusanter, S. et al. “Measurements of OH and HO2 concentrations during the MCMA-2006 field campaign – Part 2: Model comparison and radical budget.” Atmospheric Chemistry and Physics 9.18 (2009): 6655-6675.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciencesen_US
dc.contributor.approverMolina, Luisa Tan
dc.contributor.mitauthorMolina, Luisa Tan
dc.contributor.mitauthorSheehy, P.
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.orderedauthorsDusanter, S.; Vimal, D.; Stevens, P. S.; Volkamer, R.; Molina, L. T.; Baker, A.; Meinardi, S.; Blake, D.; Sheehy, P.; Merten, A.; Zhang, R.; Zheng, J.; Fortner, E. C.; Junkermann, W.; Dubey, M.; Rahn, T.; Eichinger, B.; Lewandowski, P.; Prueger, J.; Holder, H.en
dc.identifier.orcidhttps://orcid.org/0000-0002-3596-5334
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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