TRENDS IN STRATOSPHERIC HUMIDITY AND THE SENSITIVITY OF OZONE TO THESE TRENDS

Citation
Sj. Evans et al., TRENDS IN STRATOSPHERIC HUMIDITY AND THE SENSITIVITY OF OZONE TO THESE TRENDS, J GEO RES-A, 103(D8), 1998, pp. 8715-8725
Citations number
38
Categorie Soggetti
Metereology & Atmospheric Sciences","Geosciences, Interdisciplinary","Astronomy & Astrophysics",Oceanografhy,"Geochemitry & Geophysics
Volume
103
Issue
D8
Year of publication
1998
Pages
8715 - 8725
Database
ISI
SICI code
Abstract
Measurements of stratospheric water vapor and methane from the Halogen Occultation Experiment (HALOE) mounted on the Upper Atmosphere Resear ch Satellite (UARS) are used to investigate changes in stratospheric w ater vapor over the period 1992-1996 inclusive. An increase in water v apor mixing ratio is found at levels between 30 km and 65 km across th e globe which fit, to first order, a linear trend varying with altitud e from 40 parts per billion by volume per year (ppbv yr(-1)) to a maxi mum of 90 ppbv yr(-1) at 45 km. These trends appear to be greater than that expected due to the growth in tropospheric methane over the past several decades, and possible mechanisms accounting for this are disc ussed. The trend of the combined budget of 2 x CH4 + H2O is approximat ely constant with altitude with a global mean value of 61 +/- 4 ppbv y r(-1). On the basis of these estimates, sensitivity studies have been performed using a two-dimensional (2-D) radiative-chemical-dynamical m odel to assess the impact on concentrations of stratospheric ozone of this degree of change in stratospheric water vapor over timescales con sistent with doubling CO2 scenarios. We find that the impact of increa sed stratospheric water vapor is to enhance the ozone increase in the midstratosphere by similar to 1 - 2% compared to the response due to a doubling of CO2 itself of similar to 5 - 10%. In the upper stratosphe re the destruction of ozone is enhanced and the changeover from produc tion to loss is lowered to similar to 50 km (from similar to 70 km). A chemical mechanism for these processes involving enhanced OH and NO2 is identified.