Articles | Volume 8, issue 4
Atmos. Chem. Phys., 8, 871–885, 2008
Atmos. Chem. Phys., 8, 871–885, 2008

  22 Feb 2008

22 Feb 2008

The response of surface ozone to climate change over the Eastern United States

P. N. Racherla1 and P. J. Adams2 P. N. Racherla and P. J. Adams
  • 1Department of Engineering and Public Policy, Carnegie Mellon University, Pittsburgh, PA, USA
  • 2Department of Civil and Environmental Engineering, and Engineering and Public Policy, Carnegie Mellon University, Pittsburgh, PA, USA

Abstract. We investigate the response of surface ozone (O3) to future climate change in the eastern United States by performing simulations corresponding to present (1990s) and future (2050s) climates using an integrated model of global climate, tropospheric gas-phase chemistry, and aerosols. A future climate has been imposed using ocean boundary conditions corresponding to the IPCC SRES A2 scenario for the 2050s decade. Present-day anthropogenic emissions and CO2/CH4 mixing ratios have been used in both simulations while climate-sensitive emissions were allowed to vary with the simulated climate. The severity and frequency of O3 episodes in the eastern U.S. increased due to future climate change, primarily as a result of increased O3 chemical production. The 95th percentile O3 mixing ratio increased by 5 ppbv and the largest frequency increase occured in the 80–90 ppbv range; the US EPA's current 8-h ozone primary standard is 80 ppbv. The increased O3 chemical production is due to increases in: 1) natural isoprene emissions; 2) hydroperoxy radical concentrations resulting from increased water vapor concentrations; and, 3) NOx concentrations resulting from reduced PAN. The most substantial and statistically significant (p<0.05) increases in episode frequency occurred over the southeast and midatlantic U.S., largely as a result of 20% higher annual-average natural isoprene emissions. These results suggest a lengthening of the O3 season over the eastern U.S. in a future climate to include late spring and early fall months. Increased chemical production and shorter average lifetime are two consistent features of the seasonal response of surface O3, with increased dry deposition loss rates contributing most to the reduced lifetime in all seasons except summer. Significant interannual variability is observed in the frequency of O3 episodes and we find that it is necessary to utilize 5 years or more of simulation data in order to separate the effects of interannual variability and climate change on O3 episodes in the eastern United States.

Final-revised paper