COMPARISON OF CALCULATED AND MEASURED PEROXIDE DATA COLLECTED IN MARINE AIR TO INVESTIGATE PROMINENT FEATURES OF THE ANNUAL CYCLE OF OZONE IN THE TROPOSPHERE
Sa. Penkett et al., COMPARISON OF CALCULATED AND MEASURED PEROXIDE DATA COLLECTED IN MARINE AIR TO INVESTIGATE PROMINENT FEATURES OF THE ANNUAL CYCLE OF OZONE IN THE TROPOSPHERE, J GEO RES-A, 103(D11), 1998, pp. 13377-13388
Large amounts of data on the concentration of peroxides have been coll
ected in vertical profiles over the North Atlantic Ocean by a Hercules
aircraft. The measured peroxide concentrations have been compared wit
h concentrations calculated by a simple algorithm derived assuming tha
t the standing peroxide concentration is in equilibrium with its produ
ction and loss processes. In clean air where the peroxide and ozone co
ncentrations are anticorrelated throughout the profile measured and ca
lculated peroxide concentrations coincide, whereas in layers of pollut
ed air within the profile, as determined from positive ozone peroxide
correlations, calculated peroxide concentrations are greatly in excess
of measured values. Using the degree of correlation between measured
and calculated peroxide concentrations as a diagnostic, it is possible
to show that many aspects of the seasonal cycle of ozone are caused b
y in situ tropospheric chemistry. Thus the summer minimum in the seaso
nal cycle of ozone, observed at clean marine ground-based sites such a
s Mace Head, is due to photochemical destruction, and elevated levels
of ozone are associated with the transport of polluted air, on occasio
n over thousands of kilometers. Of particular interest if our analysis
is correct, the broad maximum of ozone occurring between March and Ma
y at ground-based sites has a large contribution from ozone formed by
tropospheric as well as stratospheric chemistry.