ACP Atmospheric Chemistry and Physics ACP Atmos. Chem. Phys. 1680-7324 Copernicus Publications Göttingen, Germany 10.5194/acp-11-4411-2011 Regional scale effects of the aerosol cloud interaction simulated with an online coupled comprehensive chemistry model Bangert M. 1 Kottmeier C. 1 Vogel B. 1 Vogel H. 1 Institute for Meteorology and Climate Research, Karlsruhe Institute of Technology, Karlsruhe, Germany 11 05 2011 11 9 4411 4423 Copyright: © 2011 M. Bangert et al. 2011 This work is licensed under the Creative Commons Attribution 3.0 Unported License. To view a copy of this licence, visit https://creativecommons.org/licenses/by/3.0/ This article is available from https://acp.copernicus.org/articles/11/4411/2011/acp-11-4411-2011.html The full text article is available as a PDF file from https://acp.copernicus.org/articles/11/4411/2011/acp-11-4411-2011.pdf

We have extended the coupled mesoscale atmosphere and chemistry model COSMO-ART to account for the transformation of aerosol particles into cloud condensation nuclei and to quantify their interaction with warm cloud microphysics on the regional scale. The new model system aims to fill the gap between cloud resolving models and global scale models. It represents the very complex microscale aerosol and cloud physics as detailed as possible, whereas the continental domain size and efficient codes will allow for both studying weather and regional climate. The model system is applied in a first extended case study for Europe for a cloudy five day period in August 2005. <br><br> The model results show that the mean cloud droplet number concentration of clouds is correlated with the structure of the terrain, and we present a terrain slope parameter TS to classify this dependency. We propose to use this relationship to parameterize the probability density function, PDF, of subgrid-scale cloud updraft velocity in the activation parameterizations of climate models. <br><br> The simulations show that the presence of cloud condensation nuclei (CCN) and clouds are closely related spatially. We find high aerosol and CCN number concentrations in the vicinity of clouds at high altitudes. The nucleation of secondary particles is enhanced above the clouds. This is caused by an efficient formation of gaseous aerosol precursors above the cloud due to more available radiation, transport of gases in clean air above the cloud, and humid conditions. Therefore the treatment of complex photochemistry is crucial in atmospheric models to simulate the distribution of CCN. <br><br> The mean cloud droplet number concentration and droplet diameter showed a close link to the change in the aerosol. To quantify the net impact of an aerosol change on the precipitation we calculated the precipitation susceptibility <i>β</i> for the whole model domain over a period of two days with an hourly resolution. The distribution function of <i>β</i> is slightly skewed to positive values and has a mean of 0.23. Clouds with a liquid water path LWP of approximately 0.85 kg m<sup>&minus;2</sup> are on average most susceptible to aerosol changes in our simulations with an absolute value of <i>β</i> of 1. The average <i>β</i> for LWP between 0.5 kg m<sup>&minus;2</sup> and 1 kg m<sup>&minus;2</sup> is approximately 0.4.

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