A comprehensive investigation of polar stratospheric clouds was performed on 25 January 2000 with instruments onboard a balloon gondola flown from Kiruna, Sweden. Cloud layers were repeatedly encountered at altitudes between 20 and 24 kilometers over a wide range of atmospheric temperatures (185 to 197 kelvin). Particle composition analysis showed that a large fraction of the cloud layers was composed of nitric acid trihydrate (NAT) particles, containing water and nitric acid at a molar ratio of 3:1; this confirmed that these long-sought solid crystals exist well above ice formation temperatures. The presence of NAT particles enhances the potential for chlorine activation with subsequent ozone destruction in polar regions, particularly in early and late winter.

The evolution of the aerosols in the tropical stratosphere since the beginning of the Cloud‐Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) mission in June 2006 is investigated using Cloud‐Aerosol Lidar with Orthogonal Polarization (CALIOP) lidar data. It is shown that the current operational calibration requires adjustment in the tropics. Indeed, on the basis of the assumption of pure Rayleigh scattering between 30 and 34 km the current calibration leads to an average underestimation of the scattering ratio by 6% because of the significant amount of aerosols up to 35 km altitude in the tropics, in contrast to midlatitudes. A better result is obtained by adjusting the calibration to higher altitudes, 36–39 km, where past Stratospheric Aerosol and Gas Experiment (SAGE) II extinction measurements showed an almost complete absence of aerosols. After recalibration the tropical stratospheric aerosol picture provided by CALIOP during the first 2 years of the mission reveals significant changes in the aerosol concentration associated with different transport processes. In the stratosphere the slow ascent of several volcanic layers and their meridional transport toward the subtropics are very consistent with the Brewer‐Dobson circulation. The near‐zero vertical velocity observed around 20 km during the Northern Hemisphere (NH) summer is in good agreement with radiative heating calculation. In the Tropical Tropopause Layer (TTL), weak depolarizing particles are observed during land convective periods, particularly intense over South Asia during the monsoon season. Finally, seasonal fast occurrence of apparent clean air in the TTL during the NH winter requires more investigations to understand its origin.

Polar stratospheric clouds (PSCs) play important roles in stratospheric ozone depletion during winter and spring at high latitudes (e.g., the Antarctic ozone hole). PSC particles provide sites for heterogeneous reactions that convert stable chlorine reservoir species to radicals that destroy ozone catalytically. PSCs also prolong ozone depletion by delaying chlorine deactivation through the removal of gas‐phase HNO₃ and H₂O by sedimentation of large nitric acid trihydrate (NAT) and ice particles. Contemporary observations by the spaceborne instruments Michelson Interferometer for Passive Atmospheric Sounding (MIPAS), Microwave Limb Sounder (MLS), and Cloud‐Aerosol Lidar with Orthogonal Polarization (CALIOP) have provided an unprecedented polar vortex‐wide climatological view of PSC occurrence and composition in both hemispheres. These data have spurred advances in our understanding of PSC formation and related dynamical processes, especially the firm evidence of widespread heterogeneous nucleation of both NAT and ice PSC particles, perhaps on nuclei of meteoritic origin. Heterogeneous chlorine activation appears to be well understood. Reaction coefficients on/in liquid droplets have been measured accurately, and while uncertainties remain for reactions on solid NAT and ice particles, they are considered relatively unimportant since under most conditions chlorine activation occurs on/in liquid droplets. There have been notable advances in the ability of chemical transport and chemistry‐climate models to reproduce PSC temporal/spatial distributions and composition observed from space. Continued spaceborne PSC observations will facilitate further improvements in the representation of PSC processes in global models and enable more accurate projections of the evolution of polar ozone and the global ozone layer as climate changes.

Different definitions for estimating the degree of changes in signal polarization measured by lidar measurements are used both to detect the presence of nonspherical aerosol particles and to estimate their shape and density. Our aim is to provide a tool for calculation and interpretation of changes in polarization that are due to aerosol backscatter measured by the lidar technique. An overview of several techniques used to calculate linear depolarization from two-channel lidar measurements is given. Advantages and disadvantages of each method are analyzed when we apply them on a lidar vertical profile. Systematic errors are also discussed. First, an overview of different estimations of polarizability of atmospheric molecules is given. The presence of signal with orthogonal polarization in each channel (cross talk) is a source of error in depolarization estimation. It is calculated at various degrees of contamination, and the total uncertainty on depolarization definition is retrieved.