Kamil is a 45 m diameter impact crater identified in 2008 in southern Egypt. It was generated by the hypervelocity impact of the Gebel Kamil iron meteorite on a sedimentary target, namely layered sandstones with subhorizontal bedding. We have carried out a petrographic study of samples from the crater wall and ejecta deposits collected during our first geophysical campaign (February 2010) in order to investigate shock effects recorded in these rocks. Ejecta samples reveal a wide range of shock features common in quartz‐rich target rocks. They have been divided into two categories, as a function of their abundance at thin section scale: (1) pervasive shock features (the most abundant), including fracturing, planar deformation features, and impact melt lapilli and bombs, and (2) localized shock features (the least abundant) including high‐pressure phases and localized impact melting in the form of intergranular melt, melt veins, and melt films in shatter cones. In particular, Kamil crater is the smallest impact crater where shatter cones, coesite, stishovite, diamond, and melt veins have been reported. Based on experimental calibrations reported in the literature, pervasive shock features suggest that the maximum shock pressure was between 30 and 60 GPa. Using the planar impact approximation, we calculate a vertical component of the impact velocity of at least 3.5 km s−1. The wide range of shock features and their freshness make Kamil a natural laboratory for studying impact cratering and shock deformation processes in small impact structures.

We have investigated silicate emulsions in impact glasses and impact melt rocks from the Wabar (Saudi Arabia), Kamil (Egypt), Barringer (USA), and Tenoumer (Mauritania) impact structures, and in experimentally generated impact glasses and laser‐generated glasses (MEMIN research unit) by scanning electron microscopy, electron microprobe analysis, and transmission electron microscopy. Textural evidence of silicate liquid immiscibility includes droplets of one glass disseminated in a chemically distinct glassy matrix; sharp phase boundaries (menisci) between the two glasses; deformation and coalescence of droplets; and occurrence of secondary, nanometer‐sized quench droplets in Si‐rich glasses. The compositions of the conjugate immiscible liquids (Si‐rich and Fe‐rich) are consistent with phase separation in two‐liquid fields in the general system Fe2SiO4–KAlSi3O8–SiO2–CaO–MgO–TiO2–P2O5. Major‐element partition coefficients are well correlated with the degree of polymerization (NBO/T) of the Si‐rich melt: Fe, Ca, Mg, and Ti are concentrated in the poorly polymerized, Fe‐rich melt, whereas K, Na, and Si prefer the highly polymerized, Si‐rich melt. Partitioning of Al is less pronounced and depends on bulk melt composition. Thus, major element partitioning between the conjugate liquids closely follows trends known from tholeiitic basalts, lunar basalts, and experimental analogs. The characteristics of impact melt inhomogeneity produced by melt unmixing in a miscibility gap are then compared to impact melt inhomogeneity caused by incomplete homogenization of different (miscible or immiscible) impact melts that result from shock melting of different target lithologies from the crater's melt zone, which do not fully homogenize and equilibrate due to rapid quenching. By taking previous reports on silicate emulsions in impact glasses into account, it follows that silicate impact melts of variable composition, cooling rate, and crystallization history might readily unmix during cooling, thereby rendering silicate liquid immiscibility a much more common process in the evolution of impact melts than previously recognized.

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Coesite is one of the most common and abundant high‐pressure phases occurring in impactites. The mechanism of formation of coesite and its postshock evolution is revisited in this paper based on Raman microspectroscopy, and scanning and transmission electron microscopy of a coesite‐bearing suevite from the Ries impact structure. Our data indicate that coesite forms through a single process, i.e., by crystallization from high‐pressure silica melt, and that its formation is related to fluid inclusions in precursor quartz. During the postshock phase, coesite aggregates are partially modified by annealing and interactions with fluids. In an early stage of the postshock evolution, coesite is back‐transformed to quartz and the surrounding diaplectic glass devitrifies into β‐cristobalite, which transforms into α‐cristobalite and then into microcrystalline quartz during subsequent stages of the postshock evolution. Altogether these postshock modifications result in a significant volume loss and extensional fracturing. During a late postshock stage, the fractures are filled with clay minerals due to circulation of hydrothermal fluids.