Background ozone over the United States in summer: Origin, trend, and contribution to pollution episodes

[1] Observations indicate that ozone (O-3) concentrations in surface air over the United States in summer contain a 20-45 ppbv background contribution, presumably reflecting transport from outside the North American boundary layer. We use a three-dimensional global model of tropospheric chemistry driven by assimilated meteorological observations to investigate the origin of this background and to quantify its contribution to total surface O-3 on both average and highly polluted summer days. The model simulation is evaluated with a suite of surface and aircraft observations over the United States from the summer of 1995. The model reproduces the principal features in the observed distributions of O-3 and its precursors, including frequency distributions of O-3 concentrations and the development of regional high-O-3 episodes in the eastern United States. Comparison of simulations with 1995 versus 1980 global fossil fuel emissions indicates that the model captures the previously observed decrease in the high end of the O-3 probability distribution in surface air over the United States (reflecting reduction of domestic hydrocarbon emissions) and the increase in the low end (reflecting, at least in the model, rising Asian emissions). In the model, background O-3 produced outside of the North American boundary layer contributes an average 25-35 ppbv to afternoon O-3 concentrations in surface air in the western United States. and 15-30 ppbv in the eastern United States during the summer of 1995. This background generally decays to below 15 ppbv during the stagnation conditions conducive to exceedances of the 8-hour 0.08 ppmv (80 ppbv) National Ambient Air Quality Standard (NAAQS) for O-3. A high background contribution of 25-40 ppbv is found during 9% of these exceedances, reflecting convective mixing of free tropospheric O-3 from aloft, followed by rapid production within the U. S. boundary layer. Anthropogenic emissions in Asia and Europe are found to increase afternoon O-3 concentrations in surface air over the United States by typically 4-7 ppbv, under both average and highly polluted conditions. This enhancement is particularly large (up to 14 ppbv) for O-3 concentrations in the 50-70 ppbv range, and would represent a major concern if the NAAQS were to be tightened.