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Volume 11, issue 18
Atmos. Chem. Phys., 11, 9563-9594, 2011
https://doi.org/10.5194/acp-11-9563-2011
© Author(s) 2011. This work is distributed under
the Creative Commons Attribution 3.0 License.

Special issue: The Pan European Gas-Aerosols Climate Interaction Study...

Atmos. Chem. Phys., 11, 9563-9594, 2011
https://doi.org/10.5194/acp-11-9563-2011
© Author(s) 2011. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 16 Sep 2011

Research article | 16 Sep 2011

Re-analysis of tropospheric sulfate aerosol and ozone for the period 1980–2005 using the aerosol-chemistry-climate model ECHAM5-HAMMOZ

L. Pozzoli1,*, G. Janssens-Maenhout1, T. Diehl2,3, I. Bey4, M. G. Schultz5, J. Feichter6, E. Vignati1, and F. Dentener1 L. Pozzoli et al.
  • 1European Commission, Joint Research Centre, Institute for Environment and Sustainability, Ispra, Italy
  • 2NASA Goddard Space Flight Center, Greenbelt, Maryland, USA
  • 3University of Maryland Baltimore County, Baltimore, Maryland, USA
  • 4Center for Climate Systems Modeling and Institute of Atmospheric and Climate Science, ETH Zurich, Zurich, Switzerland
  • 5Forschungszentrum Jülich, Germany
  • 6Max Planck Institute for Meteorology, Hamburg, Germany
  • *now at: Eurasia Institute of Earth Sciences, Istanbul Technical University, Turkey

Abstract. Understanding historical trends of trace gas and aerosol distributions in the troposphere is essential to evaluate the efficiency of existing strategies to reduce air pollution and to design more efficient future air quality and climate policies. We performed coupled photochemistry and aerosol microphysics simulations for the period 1980–2005 using the aerosol-chemistry-climate model ECHAM5-HAMMOZ, to assess our understanding of long-term changes and inter-annual variability of the chemical composition of the troposphere, and in particular of ozone and sulfate concentrations, for which long-term surface observations are available. In order to separate the impact of the anthropogenic emissions and natural variability on atmospheric chemistry, we compare two model experiments, driven by the same ECMWF re-analysis data, but with varying and constant anthropogenic emissions, respectively. Our model analysis indicates an increase of ca. 1 ppbv (0.055 ± 0.002 ppbv yr−1) in global average surface O3 concentrations due to anthropogenic emissions, but this trend is largely masked by the larger O3 anomalies due to the variability of meteorology and natural emissions. The changes in meteorology (not including stratospheric variations) and natural emissions account for the 75 % of the total variability of global average surface O3 concentrations. Regionally, annual mean surface O3 concentrations increased by 1.3 and 1.6 ppbv over Europe and North America, respectively, despite the large anthropogenic emission reductions between 1980 and 2005. A comparison of winter and summer O3 trends with measurements shows a qualitative agreement, except in North America, where our model erroneously computed a positive trend. Simulated O3 increases of more than 4 ppbv in East Asia and 5 ppbv in South Asia can not be corroborated with long-term observations. Global average sulfate surface concentrations are largely controlled by anthropogenic emissions. Globally natural emissions are an important driver determining AOD variations. Regionally, AOD decreased by 28 % over Europe, while it increased by 19 % and 26 % in East and South Asia. The global radiative perturbation calculated in our model for the period 1980–2005 was rather small (0.05 W m−2 for O3 and 0.02 W m−2 for total aerosol direct effect), but larger perturbations ranging from −0.54 to 1.26 W m−2 are estimated in those regions where anthropogenic emissions largely varied.

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