Rd. Saylor et al., Simulation of the tropospheric distribution of carbon monoxide during the 1984 MAPS experiment, ATMOS ENVIR, 33(28), 1999, pp. 4675-4694
A global, three-dimensional tropospheric chemistry model was used to perfor
m simulations of the tropospheric distribution of carbon monoxide (CO) coin
ciding with NASA's Measurement of Air Pollution from Satellites (MAPS) expe
riment which took place during 5-13 October 1984. Archived meteorological d
ata for September and October, 1984, were obtained from the European Centre
for Medium-Range Weather Forecasting and used to drive the offline chemica
l transport model simulations. Base-case CO emissions were generated by app
lying emission factors to compiled inventories for related or co-emitted tr
ace species. Simulation results from September and October have been compar
ed with a recent re-release of the 1984 MAPS data and with in situ correlat
ive data taken during the MAPS mission. Because of unrealistically large sp
atial variability in N2O mixing ratios measured concurrently by MAPS, model
results were also compared with an adjusted CO data set generated by assum
ing that errors in N2O measured mixing ratios were correlated with errors i
n the MAPS CO data. These comparisons, in conjunction with simulations prob
ing model sensitivities, led to the conclusion that biomass burning CO emis
sions from central and southern Africa may have been larger during Septembe
r and October, 1984, than our initial best estimate based on the CO2 emissi
ons data of Hao et al. (1990. Fire in the Tropical Biota; Ecosystem Process
es and Global Challenges. Springer, Berlin, pp. 440-462; 1994. Global Bioge
ochemical Cycles 8, 495-503). This result is in disagreement with recent es
timates of biomass burning emissions from Africa (Scholes et al., 1996, Jou
rnal of Geophysical Research 101, 23677-23682) which are smaller than previ
ously thought for emissions from this region. Although unknown model defici
encies cannot be conclusively ruled out, model sensitivity studies indicate
that increased CO emissions from central and southern Africa offer the bes
t explanation for reducing observed differences between model results and M
APS data for this time period. Our results, in combination with a disparity
in recent CO emission estimates from this region (Scholes et al., 1996; Ha
o et al., 1996, Journal of Geophysical Research 101, 23577-23584), and in l
ight of recent indications of highly variable biomass burning activities fr
om the tropical western Pacific (Folkins et al., 1997, Journal of Geophysic
al Research 102, 13291-13299), seem to suggest that biomass burning emissio
ns exhibit significant year-to-year variability. This large variability of
emissions sources makes the accurate simulation of specific time periods ve
ry difficult and suggests that biomass burning trace species inventories ma
y have to be developed specifically for each simulated time period, employi
ng satellite-derived information on fire coverage and flame intensity. (C)
1999 Elsevier Science Ltd. All rights reserved.