Geophysical Research Letters · 1999 · 50 citations · 20 references
Natural SciencesChemistryEnvironmental SciencesAtmospheric ChemistryAtmospheric ScienceSpectroscopyAir PollutantsAir Pollution ChemistryAtmospheric Oxidation ProcessesAtmospheric Radical ChemistryOzone ChemistryReactive Oxygen SpeciesAtmospheric Oxidation MechanismsConcentrationOxidant ChemistryOzoneOzone PhotochemistryPeroxy Radical ChemistryPrimary Production MechanismsRadical Production Pathways
HO 2 (hydroperoxy) radical of unexpectedly high concentration around 3 ppt was measured by an instrument based on laser‐induced fluorescence with NO addition at Oki Island, Japan, on the night of August 9/10, 1998. We confirmed that the interference by atmospheric organic peroxy (RO 2 ) radicals was insignificant and concluded that the measured signal originated from nighttime HO 2 . Model calculations constrained to ancillary measurements indicated that HO 2 and RO 2 were produced primarily via the reactions of ozone with olefins, especially those with internal olefins, and that NO 3 chemistry was relatively unimportant. HO 2 concentration was kept high by nighttime NO (∼10 ppt) via RO 2 + NO reactions. Low NO 2 (∼150 ppt) slowed NO 3 production rate. Thus, the high observed HO 2 suggests that the reactions of O 3 with olefins are important HOx primary production mechanisms in the relatively clean atmosphere.
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A new mechanism for regional atmospheric chemistry modeling
William R. Stockwell, Frank Kirchner, Michael Kühn et al. · Journal of Geophysical Research Atmospheres · 1997 · 1.2K citations · Full text