TY - JOUR
T1 - Measurements of ClO and O3 from 21°N to 61°N in the lower stratosphere during February 1988
T2 - Implications for heterogeneous chemistry
AU - King, J. C.
AU - Brune, William Henry
AU - Toohey, D. W.
AU - Rodriguez, J. M.
AU - Starr, W. L.
AU - Vedder, J. F.
PY - 1991/1/1
Y1 - 1991/1/1
N2 - 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 N2O5 on sulfate aerosols is the cause of this decadal ozone decline by comparing ClO and O3 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.
AB - 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 N2O5 on sulfate aerosols is the cause of this decadal ozone decline by comparing ClO and O3 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.
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U2 - 10.1029/91GL02628
DO - 10.1029/91GL02628
M3 - Article
AN - SCOPUS:0026283896
SN - 0094-8276
VL - 18
SP - 2273
EP - 2276
JO - Geophysical Research Letters
JF - Geophysical Research Letters
IS - 12
ER -