Impact of the deep convection of isoprene and other reactive trace species on radicals and ozone in the upper troposphere

dc.contributor.authorApel, E. C.
dc.contributor.authorOlson, J. R.
dc.contributor.authorCrawford, J. H.
dc.contributor.authorHornbrook, R. S.
dc.contributor.authorHills, A. J.
dc.contributor.authorCantrell, C. A.
dc.contributor.authorEmmons, L. K.
dc.contributor.authorKnapp, D. J.
dc.contributor.authorHall, S.
dc.contributor.authorMauldin, R. L.
dc.contributor.authorWeinheimer, A. J.
dc.contributor.authorFried, A.
dc.contributor.authorBlake, D. R.
dc.contributor.authorCrounse, J. D.
dc.contributor.authorSt. Clair, Jason
dc.contributor.authorWennberg, P. O.
dc.contributor.authorDiskin, G. S.
dc.contributor.authorFuelberg, H. E.
dc.contributor.authorWisthaler, A.
dc.contributor.authorMikoviny, T.
dc.contributor.authorBrune, W.
dc.contributor.authorRiemer, D. D.
dc.date.accessioned2020-06-18T16:11:19Z
dc.date.available2020-06-18T16:11:19Z
dc.date.issued2012-01-27
dc.description.abstractObservations of a comprehensive suite of inorganic and organic trace gases, including non-methane hydrocarbons (NMHCs), halogenated organics and oxygenated volatile organic compounds (OVOCs), obtained from the NASA DC-8 over Canada during the ARCTAS aircraft campaign in July 2008 illustrate that convection is important for redistributing both long- and short-lived species throughout the troposphere. Convective outflow events were identified by the elevated mixing ratios of organic species in the upper troposphere relative to background conditions. Several dramatic events were observed in which isoprene and its oxidation products were detected at hundreds of pptv at altitudes higher than 8 km. Two events are studied in detail using detailed experimental data and the NASA Langley Research Center (LaRC) box model. One event had no lightning NOₓ (NO + NO₂) associated with it and the other had substantial lightning NOₓ (LNOₓ > 1 ppbv). When convective storms transport isoprene from the boundary layer to the upper troposphere and no LNOₓ is present, OH is reduced due to scavenging by isoprene, which serves to slow the chemistry, resulting in longer lifetimes for species that react with OH. Ozone and PAN production is minimal in this case. In the case where isoprene is convected and LNOₓ is present, there is a large effect on the expected ensuing chemistry: isoprene exerts a dominant impact on HOₓ and nitrogen-containing species; the relative contribution from other species to HOₓ, such as peroxides, is insignificant. The isoprene reacts quickly, resulting in primary and secondary products, including formaldehyde and methyl glyoxal. The model predicts enhanced production of alkyl nitrates (ANs) and peroxyacyl nitrate compounds (PANs). PANs persist because of the cold temperatures of the upper troposphere resulting in a large change in the NOₓ mixing ratios which, in turn, has a large impact on the HOₓ chemistry. Ozone production is substantial during the first few hours following the convection to the UT, resulting in a net gain of approximately 10 ppbv compared to the modeled scenario in which LNOₓ is present but no isoprene is present aloft.en_US
dc.description.sponsorshipThe authors thank the crew and support team for the NASA DC-8 aircraft, and Mary Barth, Frank Flocke and John Orlando for helpful comments and discussion. The authors gratefully acknowledge the financial support of NASA (Grant No. X08AD33G). PTR-MS measurements were supported by the Austrian Research Promotion Agency (FFG-ALR) and the Tiroler Zukunftstiftung, and were carried out with the help/support of M. Graus, A. Hansel and T. D. Maerk. The National Center for Atmospheric Research is sponsored by the National Science Foundation. Any opinions, findings and conclusions or recommendations expressed in the publication are those of the authors and do not necessarily reflect the views of the National Science Foundation.en_US
dc.description.urihttps://www.atmos-chem-phys.net/12/1135/2012/en_US
dc.format.extent16 pagesen_US
dc.genrejournal articlesen_US
dc.identifierdoi:10.13016/m2h5vf-mb87
dc.identifier.citationApel, E. C., Olson, J. R., Crawford, J. H., Hornbrook, R. S., Hills, A. J., Cantrell, C. A., Emmons, L. K., Knapp, D. J., Hall, S., Mauldin III, R. L., Weinheimer, A. J., Fried, A., Blake, D. R., Crounse, J. D., Clair, J. M. St., Wennberg, P. O., Diskin, G. S., Fuelberg, H. E., Wisthaler, A., Mikoviny, T., Brune, W., and Riemer, D. D.: Impact of the deep convection of isoprene and other reactive trace species on radicals and ozone in the upper troposphere, Atmos. Chem. Phys., 12, 1135–1150, https://doi.org/10.5194/acp-12-1135-2012, 2012.en_US
dc.identifier.urihttps://doi.org/10.5194/acp-12-1135-2012
dc.identifier.urihttp://hdl.handle.net/11603/18922
dc.language.isoen_USen_US
dc.publisherCopernicus Publicationsen_US
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Joint Center for Earth Systems Technology
dc.rightsThis item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author.
dc.rightsAttribution 3.0 Unported*
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/*
dc.titleImpact of the deep convection of isoprene and other reactive trace species on radicals and ozone in the upper troposphereen_US
dc.typeTexten_US

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