The coupling of ClONO2, ClO, and NO2 in the lower stratosphere from in situ observations using the NASA ER-2 aircraft

The first in situ measurements of ClONO2 in the lower stratosphere, acquired using the NASA ER-2 aircraft during the Polar Ozone Loss in the Arctic Region in Summer (POLARIS) mission, are combined with simultaneous measurements of ClO, NO2, temperature, pressure, and the calculated photolysis rate c...

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Bibliographic Details
Published in:Journal of Geophysical Research Vol. 104; no. D21; pp. 26705 - 26714
Main Authors: Stimpfle, R. E., Cohen, R. C., Bonne, G. P., Voss, P. B., Perkins, K. K., Koch, L. C., Anderson, J. G., Salawitch, R. J., Gao, R. S.
Format: Journal Article
Language:English
Published: Headquarters Blackwell Publishing Ltd 20-11-1999
American Geophysical Union
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Summary:The first in situ measurements of ClONO2 in the lower stratosphere, acquired using the NASA ER-2 aircraft during the Polar Ozone Loss in the Arctic Region in Summer (POLARIS) mission, are combined with simultaneous measurements of ClO, NO2, temperature, pressure, and the calculated photolysis rate coefficient (J(sub ClONO2)) to examine the balance between production and loss of ClONO2. The observations demonstrate the ClONO2 photochemical steady state measurement, [ClONO2](sup PSS) = k[ClO][No2]/J(sub ClONO2), is in good agreement with the direct measurement, [ClONO2](sup MEAS). For the bulk of the data (80%), where T > 220 K and latitudes > 45 N, [ClONO2](sup PPS) = 1.15 +/- 0.36(1-sigma)[ClONO2](sup MEAS), while for T< 220 K and latitudes < 45 N, the result is somewhat less at 1.01 +/- 0.30. The cause of the temperature and/or latitude trend is unidentified. These results are independent of solar zenith angle and air density, thus there is no evidence in support of a pressure-dependent quantum yield for photodissociation of ClONO2 at wavelengths > 300 nm. These measurements confirm the mechanism by which active nitrogen (NOx = NO + NO2) controls the abundance of active chlorine (Clx = ClO + Cl) in the stratosphere.
Bibliography:ark:/67375/WNG-V3KDFWX8-V
ArticleID:1999JD900288
istex:F476ED57224E03A06E63E7AE68BFEC89E81A4678
HQ
Paper-1999JD900288
Headquarters
ISSN:0148-0227
2156-2202
DOI:10.1029/1999JD900288