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Measurements of ClO and O 3 from 21°N to 61°N in the lower stratosphere during February 1988: Implications for heterogeneous chemistry
Author(s) -
King J. C.,
Brune W. H.,
Toohey D. W.,
Rodriguez J. M.,
Starr W. L.,
Vedder J. F.
Publication year - 1991
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 - 10.1029/91gl02628
Subject(s) - stratosphere , middle latitudes , ozone , atmospheric chemistry , atmospheric sciences , chlorine , gas phase , ozone depletion , sulfate , latitude , ozone layer , chemistry , environmental science , climatology , environmental chemistry , geology , organic chemistry , geodesy
The decline in stratospheric ozone at northern midlatitudes in wintertime may be caused by chlorine photochemistry that has been enhanced by heterogeneous reactions. We examine the possibility that the heterogeneous reaction of N 2 O 5 on sulfate aerosols is the cause of this decadal ozone decline by comparing ClO and O 3 measurements made in the lower stratosphere during February, 1988, with results from a two‐dimensional model. At midlatitudes, the abundances, latitudinal, and seasonal gradients of the observed ClO are similar to the results of a model with heterogeneous chemistry, but are in strong disagreement with the results from the model with only gas‐phase chemistry. At low latitudes, agreement is best with the results of the model with only gas‐phase chemistry. These limited observations indicate that the amount of reactive chlorine is being enhanced, and that heterogeneous chemistry is a likely cause, but the details of the heterogeneous chemistry and the possibility of other mechanisms still need to be considered.