Where did tropospheric ozone over southern Africa and the tropical Atlantic come from in October 1992? Insights from TOMS, GTE TRACE A, and SAFARI 1992

The seasonal tropospheric ozone maximum in the tropical South Atlantic, first recognized from satellite observations [Fishman et al., 1986, 1991], Save rise to the IGAC/ STARE/SAFARI 1992/TRACE A campaigns (International Global Atmospheric Chemistry/South Tropical Atlantic Regional Experiment/Southern African Fire Atmospheric Research Initiative/Transport and Atmospheric Chemistry Near the Equator-Atlantic) in September and October 1992. Along with a new TOMS-based method for deriving tropospheric column ozone, we used the TRACE A/SAFARI 1992 data set to put together a regional picture of the O-3 distribution during this period, Sondes and aircraft profiling showed a troposphere with layers of high O-3 (greater than or equal to 90 ppbv) all the way to the tropopause. These features extend in a band from 0 degrees to 25 degrees S, over the SE Indian Ocean, Africa, the Atlantic, and eastern South America. A combination of trajectory and photochemical modeling (the Goddard (GSFC) isentropic trajectory and tropospheric point model, respectively) shows a strong connection between regions of high ozone and concentrated biomass burning, the latter identified using satellite-derived fire counts [Justice et al., this issue]. Back trajectories from a high-O-3 tropical Atlantic region (column ozone at Ascension averaged 50 Dobson units (DU)) and forward trajectories from fire-rich and convectively active areas show that the Atlantic and southern Africa are supplied with O-3 and O-3-forming trace gases by midlevel easterlies and/or recirculating air from Africa, with lesser contributions from South American burning and urban pollution. Limited sampling in the mixed layer over Namibia shows possible biogenic sources of NO, High-level westerlies from Brazil (following deep convective transport of ozone precursors to the upper troposphere) dominate the upper tropospheric O-3 budget over Natal, Ascension, and Okaukuejo (Namibia), although most enhanced O-3 (75% or more) equatorward of 10 degrees S was from Africa. Deep convection may be responsible for the timing of the seasonal tropospheric O-3 maximum: Natal and Ascension show a 1- to 2-month lag relative to the period of maximum burning [cf. Baldy et al., this issue; Olson ct al., this issue]. Photochemical model calculations constrained with TRACE A and SAFARI airborne observations of O-3 and O-3 precursors (NOx, CO, hydrocarbons) show robust ozone formation (up to 15 ppbv O-3/d or several DU/d) in a widespread, persistent, and well-mixed layer to 4 km. Slower but still positive net O-3 formation took place throughout the tropical upper troposphere [cf. Pickering et al., this issue (a); Jacob et al., this issue]. Thus whether it is faster rates of O-3 formation in source regions with higher turnover rates or slower O-3 production in long-lived stable layers ubiquitous in the TRACE A region, 10-30 DU tropospheric O-3 above a similar to 25-DU background can be accounted for, In summary, the O-3 maximum studied in October 1992 was caused by a coincidence of abundant O-3 precursors from biomass fires, a long residence time of stable air parcels over the eastern Atlantic and southern Africa, and deep convective transport of biomass burning products, with additional NO from lightning and occasionally biogenic sources.