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Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
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Volume 10, issue 2 | Copyright
Atmos. Chem. Phys., 10, 789-815, 2010
https://doi.org/10.5194/acp-10-789-2010
© Author(s) 2010. This work is distributed under
the Creative Commons Attribution 3.0 License.

  26 Jan 2010

26 Jan 2010

Global model simulations of air pollution during the 2003 European heat wave

C. Ordóñez1,2, N. Elguindi1, O. Stein3,4, V. Huijnen5, J. Flemming6, A. Inness6, H. Flentje7, E. Katragkou8, P. Moinat9, V.-H. Peuch9, A. Segers5,10, V. Thouret1, G. Athier1, M. van Weele5, C. S. Zerefos11,12, J.-P. Cammas1, and M. G. Schultz3 C. Ordóñez et al.
  • 1Laboratoire d'Aérologie, UMR5560, CNRS and Université de Toulouse, Toulouse, France
  • 2Met Office, Atmospheric Dispersion Group, Exeter, UK
  • 3FZ Jülich, Institute for Chemistry and Dynamics of the Geosphere – 2: Troposphere, Jülich, Germany
  • 4Max Planck Institute for Meteorology, Hamburg, Germany
  • 5Royal Netherlands Meteorological Institute (KNMI), De Bilt, The Netherlands
  • 6European Centre for Medium-Range Weather Forecasts (ECMWF), Reading, UK
  • 7Deutscher Wetterdienst (DWD), Observatorium Hohenpeißenberg, Germany
  • 8Laboratory of Atmospheric Physics, Aristotle University of Thessaloniki, Thessaloniki, Greece
  • 9Météo-France, Centre National de Recherches Météorologiques, Toulouse, France
  • 10TNO Built Environment and Geosciences, Department of Air Quality and Climate, Utrecht, The Netherlands
  • 11Laboratory of Climatology and Atmospheric Environment, Faculty of Geology and Geoenvironment, University of Athens, Greece
  • 12Atmospheric Environment Division, Biomedical Research Foundation of the Academy of Athens, Greece

Abstract. Three global Chemistry Transport Models – MOZART, MOCAGE, and TM5 – as well as MOZART coupled to the IFS meteorological model including assimilation of ozone (O3) and carbon monoxide (CO) satellite column retrievals, have been compared to surface measurements and MOZAIC vertical profiles in the troposphere over Western/Central Europe for summer 2003. The models reproduce the meteorological features and enhancement of pollution during the period 2–14 August, but not fully the ozone and CO mixing ratios measured during that episode. Modified normalised mean biases are around −25% (except ~5% for MOCAGE) in the case of ozone and from −80% to −30% for CO in the boundary layer above Frankfurt. The coupling and assimilation of CO columns from MOPITT overcomes some of the deficiencies in the treatment of transport, chemistry and emissions in MOZART, reducing the negative biases to around 20%. The high reactivity and small dry deposition velocities in MOCAGE seem to be responsible for the overestimation of O3 in this model. Results from sensitivity simulations indicate that an increase of the horizontal resolution to around 1°×1° and potential uncertainties in European anthropogenic emissions or in long-range transport of pollution cannot completely account for the underestimation of CO and O3 found for most models. A process-oriented TM5 sensitivity simulation where soil wetness was reduced results in a decrease in dry deposition fluxes and a subsequent ozone increase larger than the ozone changes due to the previous sensitivity runs. However this latest simulation still underestimates ozone during the heat wave and overestimates it outside that period. Most probably, a combination of the mentioned factors together with underrepresented biogenic emissions in the models, uncertainties in the modelling of vertical/horizontal transport processes in the proximity of the boundary layer as well as limitations of the chemistry schemes are responsible for the underestimation of ozone (overestimation in the case of MOCAGE) and CO found in the models during this extreme pollution event.

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