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Detailed Reference Information |
Brühl, C. and Crutzen, P.J. (2000). NOx-catalyzed ozone destruction and NOx activation at midlatitudes to high latitudes as the main cause of the spring to fall ozone decline in the northern hemisphere. Journal of Geophysical Research 105: doi: 10.1029/2000JD900069. issn: 0148-0227. |
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Recent redeterminations of the rate coefficients for the reaction O+NO2→NO+O2, the rate-limiting step in the NOx catalytic ozone destruction cycle, and two rate constants dominating the NOx/NOy ratio, OH+NO2(+M)→HNO3(+M) and OH+HNO3→H2O+NO3, have the consequence that the decline of total ozone between spring and fall, at midlatitudes to high latitudes, is even more determined by NOx-catalyzed ozone destruction than previously calculated. Their use also leads to consistent new conclusions regarding the ozone budget of the stratosphere (and ozone transport to the troposphere). Using UARS Halogen Occultation Experiment satellite data as constraints, we derive model estimates of the ozone budget of the Northern Hemisphere lower stratosphere between spring and fall. Although net chemical ozone production occurs in the latitude region between the subtropical barrier (25 ¿--30 ¿N) and 50 ¿N, total ozone declines in this region because of transport to higher latitudes and to the troposphere. North of 50 ¿N, strong chemical ozone loss leads to total ozone loss as well. The tropical region appears not to play a significant role in seasonal total ozone variation. ¿ 2000 American Geophysical Union |
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Abstract |
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Keywords
Atmospheric Composition and Structure, Atmospheric Composition and Structure, Chemical kinetic and photochemical properties, Atmospheric Composition and Structure, Constituent sources and sinks, Atmospheric Composition and Structure, Middle atmosphere—composition and chemistry, Atmospheric Composition and Structure, Cloud physics and chemistry |
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Publisher
American Geophysical Union 2000 Florida Avenue N.W. Washington, D.C. 20009-1277 USA 1-202-462-6900 1-202-328-0566 service@agu.org |
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