Abstract. Snow in the environment acts as a host to rich chemistry and provides a matrix for physical exchange of contaminants within the ecosystem. The goal of this review is to summarise the current state of knowledge of physical processes and chemical reactivity in surface snow with relevance to polar regions. It focuses on a description of impurities in distinct compartments present in surface snow, such as snow crystals, grain boundaries, crystal surfaces, and liquid parts. It emphasises the microscopic description of the ice surface and its link with the environment. Distinct differences between the disordered air–ice interface, often termed quasi-liquid layer, and a liquid phase are highlighted. The reactivity in these different compartments of surface snow is discussed using many experimental studies, simulations, and selected snow models from the molecular to the macro-scale. Although new experimental techniques have extended our knowledge of the surface properties of ice and their impact on some single reactions and processes, others occurring on, at or within snow grains remain unquantified. The presence of liquid or liquid-like compartments either due to the formation of brine or disorder at surfaces of snow crystals below the freezing point may strongly modify reaction rates. Therefore, future experiments should include a detailed characterisation of the surface properties of the ice matrices. A further point that remains largely unresolved is the distribution of impurities between the different domains of the condensed phase inside the snowpack, i.e. in the bulk solid, in liquid at the surface or trapped in confined pockets within or between grains, or at the surface. While surface-sensitive laboratory techniques may in the future help to resolve this point for equilibrium conditions, additional uncertainty for the environmental snowpack may be caused by the highly dynamic nature of the snowpack due to the fast metamorphism occurring under certain environmental conditions. Due to these gaps in knowledge the first snow chemistry models have attempted to reproduce certain processes like the long-term incorporation of volatile compounds in snow and firn or the release of reactive species from the snowpack. Although so far none of the models offers a coupled approach of physical and chemical processes or a detailed representation of the different compartments, they have successfully been used to reproduce some field experiments. A fully coupled snow chemistry and physics model remains to be developed.

Sintering of ice is driven by the thermodynamic requirement to decrease surface energy. The structural morphology of ice in nature has many forms-from snowflakes to glaciers. These forms and their evolution depend critically on the balance between the thermodynamic and kinetic factors involved. Ice is a crystalline material so scientific understanding and approaches from more conventional materials can be applied to ice. The early models of solid state ice sintering are based on power law models originally developed in metallurgy. For pressure sintering of ice, these are based on work on hot isostatic pressing of metals and ceramics. Recent advances in recognizing the grain boundary groove geometry between sintering ice particles require models that use new approaches in materials science. The newer models of sintering in materials science are beginning to incorporate more realistic processing conditions and microstructural complexity, and so there is much to be gained from applying these to ice in the future. The vapour pressure of ice is high, which causes it to sublime readily. The main mechanism for isothermal sintering of ice particles is by vapour diffusion; however other transport mechanisms certainly contribute. Plastic deformation with power law creep combined with recrystallization become important mechanisms in sintering with external pressure. Modern experimental techniques, low temperature scanning electron microscopy and x-ray tomography, are providing new insights into the evolution of microstructures in ice. Sintering in the presence of a small volume fraction of the liquid phase causes much higher bond growth rates. This may be important in natural snow which contains impurities that form a liquid phase. Knowledge of ice microstructure and sintering is beneficial in understanding mechanical behaviour in ice friction and the stability of snow slopes prone to avalanches.

We show that the plastic deformation of snow under uniaxial compression is characterized by complex spatio-temporal strain localization phenomena. Deformation is characterized by repeated nucleation and propagation of compaction bands. Compaction bands are also observed during the very first stage of compression of solid foams where a single band moves across the sample at approximately constant stress. However, snow differs from these materials as repeated nucleation and propagation of bands occurs throughout the subsequent hardening stage until the end of the deformation experiment. Band nucleation and/or reflection of bands at the sample boundaries are accompanied by stress drops which punctuate the stress strain curve. A constitutive model is proposed which quantitatively reproduces all features of this oscillatory deformation mode. To this end, a well-established compressive plasticity framework for solid foams is generalized to account for shear softening behavior, time dependence of microstructure ('rapid sintering') and non-locality of damage processes in snow. arXiv:1501.02184v1 [cond-mat.soft]

International audienceIn this work, we present first results of high-resolution EBSD for ice with a spatial resolution down to 0.25 μm. The study highlights the potential of EBSD to significantly increase our understanding of deformation and annealing processes associated with the build-up of internal stresses due to strain incompatibility between grains. Two polycrystalline samples were analyzed: a natural sample of polar ice from the Vostok ice core (Antarctica) and an experimentally deformed sample of laboratory grown columnar ice. In summary, we observe the following: (1) inhomogeneous deformation through the grains is translated into lattice distortions that are concentrated mainly at grain boundaries and triple junctions (natural and experimental sample), (2) these distortions may be continuous (natural and experimental sample) or may form distinct tilt boundaries and sub-grains of 10–50 μm size (experimental sample). These form mainly by rearrangement of basal edge dislocations into low-energy configurations (i.e. tilt boundaries) in various prism planes. Continuous lattice distortions originate from screw or mixed edge and screw dislocations lying in the basal plane

Ice and snow in the environment are important because they not only act as a host to rich chemistry but also provide a matrix for physical exchanges of contaminants within the ecosystem. This review discusses how the structure of snow influences both chemical reactivity and physical processes, which thereby makes snow a unique medium for study. The focus is placed on impacts of the presence of liquid and surface disorder using many experimental studies, simulations, and field observations from the molecular to the micro-scale