Abstract. Satellite-based observations during the Arctic winter of 2009/2010 provide firm evidence that, in contrast to the current understanding, the nucleation of nitric acid trihydrate (NAT) in the polar stratosphere does not only occur on preexisting ice particles. In order to explain the NAT clouds observed over the Arctic in mid-December 2009, a heterogeneous nucleation mechanism is required, occurring via immersion freezing on the surface of solid particles, likely of meteoritic origin. For the first time, a detailed microphysical modelling of this NAT formation pathway has been carried out. Heterogeneous NAT formation was calculated along more than sixty thousand trajectories, ending at Cloud Aerosol Lidar with Orthogonal Polarization (CALIOP) observation points. Comparing the optical properties of the modelled NAT with these observations enabled a thorough validation of a newly developed NAT nucleation parameterisation, which has been built into the Zurich Optical and Microphysical box Model (ZOMM). The parameterisation is based on active site theory, is simple to implement in models and provides substantial advantages over previous approaches which involved a constant rate of NAT nucleation in a given volume of air. It is shown that the new method is capable of reproducing observed polar stratospheric clouds (PSCs) very well, despite the varied conditions experienced by air parcels travelling along the different trajectories. In a companion paper, ZOMM is applied to a later period of the winter, when ice PSCs are also present, and it is shown that the observed PSCs are also represented extremely well under these conditions.

Abstract. This paper provides compelling evidence for the importance of heterogeneous nucleation, likely on solid particles of meteoritic origin, and of small-scale temperature fluctuations, for the formation of ice particles in the Arctic stratosphere. During January 2010, ice PSCs (polar stratospheric clouds) were shown by CALIPSO (Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations) to have occurred on a synoptic scale (~1000 km dimension). CALIPSO observations also showed widespread PSCs containing NAT (nitric acid trihydrate) particles in December 2009, prior to the occurrence of synoptic-scale regions of ice PSCs during mid-January 2010. We demonstrate by means of detailed microphysical modeling along air parcel trajectories that the formation of these PSCs is not readily reconciled with expectations from the conventional understanding of PSC nucleation mechanisms. The measurements are at odds with the previous laboratory-based understanding of PSC formation, which deemed direct heterogeneous nucleation of NAT and ice on preexisting solid particles unlikely. While a companion paper (Part 1) addresses the heterogeneous nucleation of NAT during December 2009, before the existence of ice PSCs, this paper shows that also the large-scale occurrence of stratospheric ice in January 2010 cannot be explained merely by homogeneous ice nucleation but requires the heterogeneous nucleation of ice, e.g. on meteoritic dust or preexisting NAT particles. The required efficiency of the ice nuclei is surprisingly high, namely comparable to that of known tropospheric ice nuclei such as mineral dust particles. To gain model agreement with the ice number densities inferred from observations, the presence of small-scale temperature fluctuations, with wavelengths unresolved by the numerical weather prediction models, is required. With the derived rate parameterization for heterogeneous ice nucleation we are able to explain and reproduce CALIPSO observations throughout the entire Arctic winter 2009/2010.

Abstract. The volcanic aerosol plume resulting from the Ey-

Abstract. Nitric acid trihydrate (NAT) particles in the polar stratosphere have been shown to be responsible for vertical redistribution of reactive nitrogen (NO y ). Recent observations by Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) aboard the CALIPSO satellite have been explained in terms of heterogeneous nucleation of NAT on foreign nuclei, revealing this to be an important formation pathway for the NAT particles. In state of the art global-or regional-scale models, heterogeneous NAT nucleation is currently simulated in a very coarse manner using a constant, saturation-independent nucleation rate. Here we present first simulations for the Arctic winter 2009/2010 applying a new saturation-dependent parametrisation of heterogeneous NAT nucleation rates within the Chemical Lagrangian Model of the Stratosphere (CLaMS). The simulation shows good agreement of chemical trace species with in situ and remote sensing observations. The simulated polar stratospheric cloud (PSC) optical properties agree much better with CALIOP observations than those simulated with a constant nucleation rate model. A comparison of the simulated particle size distributions with observations made using the Forward Scattering Spectrometer Probe (FSSP) aboard the high altitude research aircraft Geophysica, shows that the model reproduces the observed size distribution, except for the very largest particles above 15 µm diameter. The vertical NO y redistribution caused by the sedimentation of the NAT particles, in particular the denitrification and nitrification signals observed by the ACE-FTS satellite instrument and the in situ SIOUX instrument aboard the Geophysica, are reproduced by the improved model, and a small improvement with respect to the constant nucleation rate model is found.