Kyshtymites are the unique corundum-blue sapphire-bearing variety of anorthosites of debatable geological origin found in the Ilmenogorsky-Vishnevogorsky complex (IVC) in the South Urals, Russia. Their mineral association includes corundum-sapphire, plagioclase (An_61–93), muscovite, clinochlore, and clinozoisite. Zircon, churchite-(Y), monazite-(Ce), and apatite group minerals are found as accessory phases. Besides, churchite-(Y) and zircon are also identified as syngenetic solid inclusions within the sapphires. In situ Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS) U-Pb zircon geochronology showed the ages at about 290–330 Ma linked to the Hercynian orogeny in IVC. These ages are close to those of the syenitic and carbonatitic magmas of the IVC, pointing to their syngenetic origin, which is in agreement with the trace element geochemistry of the zircons demonstrating clear magmatic signature. However, the trace element composition of sapphires shows mostly metamorphic signature with metasomatic overprints in contrast to the geochemistry of zircons. The reason for this discrepancy can be the fact that the discrimination diagrams for sapphires are not as universal as assumed. Hence, they cannot provide an unambiguous determination of sapphire origin. If it is true and zircons can be used as traces of anorthosite genesis, then it can be suggested that kyshtymites are formed in a magmatic process at 440–420 Ma ago, most probably as plagioclase cumulates in a magma chamber. This cumulate rock was affected by a second magmatic event at 290–330 Ma as recorded in zircon and sapphire zoning. On the other hand, Ti-in-zircon thermometer indicates that processes operated at relatively lower temperature (<900 °C), which is not enough to re-melt the anorthosites. Hence, zircons in kyshtymites can be magmatic but inherited from another rock, which was re-worked during metamorphism. The most probable candidate for the anorthosite protolith is carbonatites assuming that metamorphic fluids could likely leave Al- and Si-rich residue, but removed Ca and CO₂. Further, Si is consumed by the silicification of ultramafic host rocks. However, kyshtymites do not show clear evidence of pronounced metasomatic zonation and evidence for large volume changes due to metamorphic alteration of carbonatites. Thus, the obtained data still do not allow for univocal reconstruction of the kyshtymite origin and further investigations are required.

This paper reports the results of the first study of pyroxenes from the deepest zones of the Lovozero deposit. The geochemical and mineralogical study of these rocks is of great scientific interest, as they are the least differentiated rocks and provide insight into the composition of a parental magma. According to microprobe analysis, clinopyroxenes evolve from early diopside–hedenbergite–augite to later alkaline aegirine–augite species. Upsection, the contents of Na, Fe³⁺ and Ti increase, while Mg, Ca, Fe²⁺, and Zr decrease. Thus, isomorphic substitution in pyroxenes of the lower zone follows the scheme (Ca, Mg, Fe²⁺, Zr) → (Na, Fe³⁺, Ti).

–New geochemical, mineralogical, and Rb–Sr and Sm–Nd isotopic data have been obtained on corundum plagioclasites–kyshtymites from the 5th Versta deposit (South Urals, Russia). The genetic...

The paper presents pioneering data on the composition of pyroxenes and the distribution of trace elements in this mineral in small geological bodies that were formed by single magma injections and their subsequent rapid crystallization: the Niva intrusion and an agpaitic syenite dyke. The pyroxene is highly alkaline and shows continuous compositional trends with an increase in the aegirine concentration. The Ti concentrations of the pyroxene are much higher than in pyroxenes in agpaitic syenites in other alkaline complexes. In spite of the fact that the pyroxene is hosted in small bodies, the evolution of these pyroxenes was similar to that of pyroxenes in the Lovozero and Khibina alkaline massifs.