O. Hov et F. Flatoy, CONVECTIVE REDISTRIBUTION OF OZONE AND OXIDES OF NITROGEN IN THE TROPOSPHERE OVER EUROPE IN SUMMER AND FALL, Journal of atmospheric chemistry, 28(1-3), 1997, pp. 319-337
The fluxes of ozone and NOx out of the atmospheric boundary layer (ABL
) over Europe are calculated in a mesoscale chemical transport model (
MCT) and compared with the net chemical production or destruction of o
zone and the emissions of precursors within the ABL for two 10 days' p
eriods which had quite different synoptic situations and levels of pho
tochemical activity (1-10 July 1991 (JUL91) and 26 October-4 November
1994 (ON94)). Over the European continent, about 8% of the NOx emissio
ns were brought from the ABL to the free troposphere as NOx, while abo
ut 15% of the NOx emissions were brought to the free troposphere as NO
y-NOx, i.e. as PAN or HNO3. The convection dominates over the synoptic
scale vertical advection as a transport mechanism both for NOx and NO
y out of the boundary layer in the summertime high pressure situation
(JUL91), while in the fall situation (ON94) the convective part was ca
lculated to be the smallest. NOx was almost completely transformed to
NOy-NOx or removed within the ABL. Also for NOy the major part of the
atmospheric cycle is confined to the ABL both for JUL91 and ON94. The
vertical transport time out of the ABL is of the order of 100 h both f
or the total model domain and over the European continent. The net con
vective exchange of ozone from the ABL is not a dominant process for t
he amount of ozone in the ABL averaged over 10 days and the whole doma
in, but convection reduces the maximum ozone concentration in episodes
significantly. The ozone producing efficiency of NOx is calculated to
increase with height to typically 15-20 in the upper half of the trop
osphere from around 5 in the ABL, but in the middle free troposphere t
he concentration of NOx is often too low to cause net chemical formati
on of ozone there.