Atmos. Chem. Phys. Discuss., 11, 14183-14220, 2011
www.atmos-chem-phys-discuss.net/11/14183/2011/
doi:10.5194/acpd-11-14183-2011
© Author(s) 2011. This work is distributed
under the Creative Commons Attribution 3.0 License.
Review Status
This discussion paper has been under review for the journal Atmospheric Chemistry and Physics (ACP). Please refer to the corresponding final paper in ACP.
Evaluation of a three-dimensional chemical transport model (PMCAMx) in the European domain during the EUCAARI May 2008 campaign
C. Fountoukis1, P. N. Racherla2, H. A. C. Denier van der Gon3, P. Polymeneas4, P. E. Haralabidis4, A. Wiedensohler5, C. Pilinis4, and S. N. Pandis1,6,7
1Institute of Chemical Engineering and High Temperature Chemical Processes, Foundation for Research and Technology Hellas (FORTH), Patras, Greece
2NASA Goddard Institute for Space Studies, New York, NY 10025, USA
3TNO Built Environment and Geosciences, Princetonlaan 6, 3584 CB Utrecht, The Netherlands
4Department of Environment, University of the Aegean, University Hill, 81100, Mytilene, Greece
5Leibniz Institute for Tropospheric Research, 04318 Leipzig, Germany
6Department of Chemical Engineering, University of Patras, Patras, Greece
7Department of Chemical Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA

Abstract. PMCAMx-2008, a detailed three dimensional chemical transport model (CTM), was applied to Europe to simulate the mass concentration and chemical composition of particulate matter (PM) during May 2008. The model includes a state-of-the-art organic aerosol module which is based on the volatility basis set framework treating both primary and secondary organic components to be semivolatile and photochemically reactive. The model performance is evaluated against high time resolution aerosol mass spectrometer (AMS) ground and airborne measurements. Overall, organic aerosol is predicted to account for 32% of total PM1 at ground level during May 2008, followed by sulfate (30%), crustal material and sea-salt (14%), ammonium (13%), nitrate (7%), and elemental carbon (4%). The model predicts that fresh primary OA (POA) is a small contributor to organic PM concentrations in Europe during late spring, and that oxygenated species (oxidized primary and biogenic secondary) dominate the ambient OA. The Mediterranean region is the only area in Europe where sulfate concentrations are predicted to be much higher than the OA, while organic matter is predicted to be the dominant PM1 species in Central and Northern Europe. The comparison of the model predictions with the ground measurements in four measurement stations is encouraging. The model reproduces more than 94% of the daily averaged data and more than 87% of the hourly data within a factor of 2 for PM1 OA. The model tends to predict relatively flat diurnal profiles for PM1 OA in many areas, both rural and urban, in agreement with the available measurements. The model performance against the high time resolution airborne measurements at multiple altitudes and locations is as good as its performance against the ground level hourly measurements. There is no evidence of missing sources of OA aloft over Europe during this period.

Citation: Fountoukis, C., Racherla, P. N., Denier van der Gon, H. A. C., Polymeneas, P., Haralabidis, P. E., Wiedensohler, A., Pilinis, C., and Pandis, S. N.: Evaluation of a three-dimensional chemical transport model (PMCAMx) in the European domain during the EUCAARI May 2008 campaign, Atmos. Chem. Phys. Discuss., 11, 14183-14220, doi:10.5194/acpd-11-14183-2011, 2011.
 
Search ACPD
Discussion Paper
    XML
    Citation
    Final Revised Paper
    Share