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Airborne in‐situ OH and HO 2 observations in the cloud‐free troposphere and lower stratosphere during SUCCESS
Author(s) -
Brune W. H.,
Faloona I. C.,
Tan D.,
Weinheimer A. J.,
Campos T.,
Ridley B. A.,
Vay S. A.,
Collins J. E.,
Sachse G. W.,
Jaeglé L.,
Jacob D. J.
Publication year - 1998
Publication title -
geophysical research letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.007
H-Index - 273
eISSN - 1944-8007
pISSN - 0094-8276
DOI - 10.1029/97gl03098
Subject(s) - stratosphere , troposphere , hydroperoxyl , atmospheric sciences , environmental science , climatology , meteorology , radical , chemistry , geology , physics , organic chemistry
The hydroxyl (OH) and hydroperoxyl (HO 2 ) radicals were measured for the first time throughout the troposphere and in the lower stratosphere with a new instrument aboard the NASA DC‐8 aircraft during the 1996 SUCCESS mission. Typically midday OH was 0.1‐0.5 pptv and HO 2 was 3‐15 pptv. Comparisons with a steady‐state model yield the following conclusions. First, even in the lower stratosphere OH was sensitive to the albedo of low clouds and distant high clouds. Second, although sometimes in agreement with models, observed OH and HO 2 were more than 4 times larger at other times. Evidence suggests that for the California upper troposphere on 10 May this discrepancy was due to unmeasured HO x sources from Asia. Third, observed HO 2 /OH had the expected inverse dependence with NO, but was inexplicably higher than modeled HO 2 /OH by an average of 30%. Finally, small‐scale, midday OH and HO 2 features were strongly linked to NO variations.