spheric models to reproduce observed atmospheric perturbations generated by SPEs, particularly with respect to NO y and ozone changes. We have further assessed the meteorological conditions and their implications for the chemical response to the SPE in both the models and observations by comparing temperature and tracer (CH 4 and CO) fields.Simulated SPE-induced ozone losses agree on average within 5 % with the observations. Simulated NO y enhancements around 1 hPa, however, are typically 30 % higher than indicated by the observations which are likely to be related to deficiencies in the used ionization rates, though other error sources related to the models' atmospheric background state and/or transport schemes cannot be excluded. The analysis of the observed and modeled NO y partitioning in the aftermath of the SPE has demonstrated the need to implement additional ion chemistry (HNO 3 formation via ion-ion recombination and water cluster ions) into the chemical schemes. An overestimation of observed H 2 O 2 enhancements by all models hints at an underestimation of the OH/HO 2 ratio in the upper polar stratosphere during the SPE. The analysis of chlorine species perturbations has shown that the encountered Published by Copernicus Publications on behalf of the European Geosciences Union. 9090 B. Funke et al.: HEPPA intercomparison study differences between models and observations, particularly the underestimation of observed ClONO 2 enhancements, are related to a smaller availability of ClO in the polar night region already before the SPE. In general, the intercomparison has demonstrated that differences in the meteorology and/or initial state of the atmosphere in the simulations cause a relevant variability of the model results, even on a short timescale of only a few days.

We evaluate the influence of the galactic cosmic rays (GCR), solar proton events (SPE), and energetic electron precipitation (EEP) on chemical composition of the atmosphere, dynamics, and climate using the chemistry-climate model SOCOL. We have carried out two 46-year long runs. The reference run is driven by a widely employed forcing set and, for the experiment run, we have included additional sources of NO x and HO x caused by all considered energetic particles. The results show that the effects of the GCR, SPE, and EEP fluxes on the chemical composition are most pronounced in the polar mesosphere and upper stratosphere; however, they are also detectable and statistically significant in the lower atmosphere consisting of an ozone increase up to 3 % in the troposphere and ozone depletion up to 8 % in the middle stratosphere. The thermal effect of the ozone depletion in the stratosphere propagates down, leading to a warming by up to 1 K averaged over 46 years over Europe during the winter season. Our results suggest that the energetic particles are able to affect atmospheric chemical composition, dynamics, and climate.

Abstract. This study investigates the influence of the Galactic Cosmic Rays (GCRs) on the atmospheric composition, temperature and dynamics by means of the 3-D Chemistry Climate Model (CCM) SOCOL v2.0. Ionization rates were parameterized according to CRAC:CRII (Cosmic Ray induced Cascade: Application for Cosmic Ray Induced Ionization), a detailed state-of-the-art model describing the effects of GCRs in the entire altitude range of the CCM from 0-80 km. We find statistically significant effects of GCRs on tropospheric and stratospheric NO x , HO x , ozone, temperature and zonal wind, whereas NO x , HO x and ozone are annually averaged and the temperature and the zonal wind are monthly averaged. In the Southern Hemisphere, the model suggests the GCR-induced NO x increase to exceed 10 % in the tropopause region (peaking with 20 % at the pole), whereas HO x is showing a decrease of about 3 % caused by enhanced conversion into HNO 3 . As a consequence, ozone is increasing by up to 3 % in the relatively unpolluted southern troposphere, where its production is sensitive to additional NO x from GCRs. Conversely, in the northern polar lower stratosphere, GCRs are found to decrease O 3 by up to 3 %, caused by the additional heterogeneous chlorine activation via ClONO 2 + HCl following GCR-induced production of ClONO 2 . There is an apparent GCR-induced acceleration of the zonal wind of up to 5 m s −1 in the Northern Hemisphere below 40 km in February, and a deceleration at higher altitudes with peak values of 3 m s −1 around 70 km altitude. The model also indentifies GCR-induced changes in the surface air, with warming in the eastern part of Europe and in Russia (up to 2.25 K for March values) and cooling in SiberiaCorrespondence to: M. Calisto (marco.calisto@env.ethz.ch) and Greenland (by almost 2 K). We show that these surface temperature changes develop even when the GCR-induced ionization is taken into account only above 18 km, suggesting that the stratospherically driven strengthening of the polar night jet extends all the way down to the Earth's surface.

We evaluate the influence of the galactic cosmic rays (GCR), solar proton events (SPE), and energetic electron precipitation (EEP) on chemical composition of the atmosphere, dynamics, and climate using the chemistry-climate model SOCOL. We have carried out two 46-year long runs. The reference run is driven by a widely employed forcing set and, for the experiment run, we have included additional sources of NO x and HO x caused by all considered energetic particles. The results show that the effects of the GCR, SPE, and EEP fluxes on the chemical composition are most pronounced in the polar mesosphere and upper stratosphere; however, they are also detectable and statistically significant in the lower atmosphere consisting of an ozone increase up to 3 % in the troposphere and ozone depletion up to 8 % in the middle stratosphere. The thermal effect of the ozone depletion in the stratosphere propagates down, leading to a warming by up to 1 K averaged over 46 years over Europe during the winter season. Our results suggest that the energetic particles are able to affect atmospheric chemical composition, dynamics, and climate. Keywords Energetic particles Á Atmospheric chemistry Á Dynamics Á Climate Á Modeling 1 Introduction Understanding of the past climate change and forecasting of the future climate requires a clear quantification of the contribution from all relevant anthropogenic and natural forcing. The contribution of energetic particles to climate change is a not well known and

We have compared composition changes of NO, NO₂, H₂O₂, O₃, N₂O, HNO₃, N₂O₅, HNO₄, ClO, HOCl, and ClONO₂ as observed by the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on Envisat in the aftermath of the "Halloween" solar proton event (SPE) in October/November 2003 at 25–0.01 hPa in the Northern Hemisphere (40–90&deg; N) and simulations performed by the following atmospheric models: the Bremen 2d Model (B2dM) and Bremen 3d Chemical Transport Model (B3dCTM), the Central Aerological Observatory (CAO) model, FinROSE, the Hamburg Model of the Neutral and Ionized Atmosphere (HAMMONIA), the Karlsruhe Simulation Model of the Middle Atmosphere (KASIMA), the ECHAM5/MESSy Atmospheric Chemistry (EMAC) model, the modeling tool for SOlar Climate Ozone Links studies (SOCOL and SOCOLi), and the Whole Atmosphere Community Climate Model (WACCM4). The large number of participating models allowed for an evaluation of the overall ability of atmospheric models to reproduce observed atmospheric perturbations generated by SPEs, particularly with respect to NO_y and ozone changes. We have further assessed the meteorological conditions and their implications on the chemical response to the SPE in both the models and observations by comparing temperature and tracer (CH₄ and CO) fields. <br><br> Simulated SPE-induced ozone losses agree on average within 5% with the observations. Simulated oy enhancements around 1 hPa, however, are typically 30% higher than indicated by the observations which can be partly attributed to an overestimation of simulated electron-induced ionization. The analysis of the observed and modeled NO_y partitioning in the aftermath of the SPE has demonstrated the need to implement additional ion chemistry (HNO₃ formation via ion-ion recombination and water cluster ions) into the chemical schemes. An overestimation of observed H₂O enhancements by all models hints at an underestimation of the OH/HO₂ ratio in the upper polar stratosphere during the SPE. The analysis of chlorine species perturbations has shown that the encountered differences between models and observations, particularly the underestimation of observed ClONO₂ enhancements, are related to a smaller availability of ClO in the polar night region already before the SPE. In general, the intercomparison has demonstrated that differences in the meteorology and/or initial state of the atmosphere in the simulations causes a relevant variability of the model results, even on a short timescale of only a few days