A series of precise nondestructive analytical methods (Raman spectroscopy, cathodoluminescence, and EBSD—electron backscatter diffraction) has been employed to investigate the internal textures of kyanite porphyroblasts from diamondiferous and diamond‐free ultrahigh‐pressure metamorphic rocks (Kokchetav massif, Northern Kazakhstan). Such internal kyanite characteristics as twinning, radial fibrous pattern, and spotty zoning were identified by means of Raman and cathodoluminescence imaging, whereas an intergrowth of two kyanite crystals was distinguished only by Raman imaging. The EBSD analysis recorded an ~10–25° changing of orientations along the elongation in the investigated kyanite porphyroblasts. The absence of a radial fibrous pattern and a spotty zoning on the EBSD maps indicates that these textures are not related to variations in crystallographic orientation. The absence of clear zoning patterns (cores, mantles, and rims) on the Raman, cathodoluminescence, or EBSD maps of the kyanite porphyroblasts indicates the rapid single‐stage formation of these porphyroblasts near the peak metamorphic conditions and the lack of recrystallization processes. The obtained results provide important implications for deciphering of mineral internal textures, showing that the data obtained by cathodoluminescence mapping can be clearly reproduced by Raman imaging, with the latter method occasionally being even more informative. This observation is of significant importance for the study of minerals that are unexposed on a thin section surface or Fe‐ and Ni‐rich minerals that do not show luminescence emission. The combination of the Raman spectroscopic, cathodoluminescence, and EBSD techniques may provide better spatial resolution for distinguishing different domains and textural peculiarities of mineral than the selective application of individual approaches.

Graphite cuboids are abundant in ultrahigh-pressure metamorphic rocks and are generally interpreted as products of partial or complete graphitization of pre-existing diamonds. The understanding of the graphite cuboid structure and its formation mechanisms is still very limited compared to nanotubes, cones, and other carbon morphologies. This paper is devoted to the natural occurrences of graphite cuboids in several metamorphic and magmatic rocks, including diamondiferous metamorphic assemblages. The studied cuboids are polycrystalline aggregates composed either of numerous smaller graphite cuboids with smooth surfaces or graphite flakes radiating from a common center. Silicates, oxides, and sulphides are abundant in all the samples studied, testifying that the presence of oxygen, sulfur, or sulphides in natural systems does not prevent the spherulitic growth of graphite. The surface topography and internal morphology of graphite cuboids combined with petrological data suggest that graphite cuboids originated from a magmatic or metamorphic fluid/melt and do not represent products of diamond-graphite transformation processes, even in diamond-bearing rocks.

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Pyrope xenocrysts (N = 52) with associated inclusions of Ti-and/or Cr-rich oxide minerals from the Aldanskaya dyke and Ogonek diatreme (Chompolo field, southeastern Siberian craton) have been investigated. The majority of xenocrysts are of lherzolitic paragenesis and have concave-upwards (normal) REE N patterns with increase in concentration from LREE to M-HREE (Group 1). Four Ca-rich (5.7-7.4 wt.% CaO) pyropes are extremely low in Ti, Na, Y and have sinusoidal REE N spectra, thus exhibiting distinct geochemical signatures (Group 2). A peculiar xenocryst s165 is the only sample to show harzburgitic derivation, whilst demonstrating normal to weakly sinusoidal REE N pattern and the highest Zr (93 ppm) and Sc (471 ppm). Chromite-magnesiochromite, rutile, Mg-ilmenite, and crichtonite-group minerals comprise a suite of oxide mineral inclusions in the pyrope xenocrysts. These minerals are characteristically enriched in Cr with 0.6-7.2 wt.% Cr 2 O 3 in rutile, 0.7-3.6 wt.% in Mg-ilmenite and 7.1-18.0 wt.% in the crichtonite-group minerals. The LILE-enriched complex titanates of the crichtonite group are high in Al 2 O 3 (0.9-2.2 wt.%), ZrO 2 (1.5-5.4 wt.%) and comprise a trend of compositions from the Ca-Sr-specific varieties to the Ba-dominant species (e.g. lindsleyite). In the studied pyrope xenocrysts the oxides coexist with silicates (clino-and orthopyroxene, olivine), hydrous silicates (talc, phlogopite, amphibole), carbonate (magnesite), sulfides (pentlandite, chalcopyrite, breakdown products of monosulfide and bornite solid solutions), apatite and graphite. P-T estimates imply the inclusion-bearing pyrope xenocrysts to have been derived from low-T peridotite assemblages that resided at ~600-800 °C and a pressure range of ~25-35 kbar in the graphite stability field. The pyrope genesis is linked to the metasomatic enrichment of peridotite protoliths by Ca-Zr-LILE-bearing percolating fluid-melt phases containing significant volatile components. These metasomatic agents are likely volatile-rich melts or supercritical C-O-H-S fluids that were released from a Paleo-subduction slab.

Two minerals of boron, dumortierite and tourmaline, have been studied in a diamondiferous kyanite gneiss (Barchi‐Kol area, Kokchetav massif, Northern Kazakhstan) by Raman spectroscopy and electron microprobe (EMP) analysis. Dumortierite and tourmaline (almost pure schorl end‐member) coexist within the sample, with blue/purple dumortierite inclusions hosted by kyanite porphyroblasts and blue tourmaline crystals occurring as inclusions in garnet. Optically, dumortierite appears almost identical to kyanite host and can be easily overlooked in thin sections during optical and scanning electron microscopic observations. Both boron minerals show a very strong anisotropy, and the most prominent Raman spectra can be obtained if the electric field vector E is parallel to the c axis of the dumortierite and tourmaline crystals. The Raman spectra of the investigated dumortierite are very similar to those of the synthetic dumortierite with a pronounced excess of boron (up to 0.26 [4]B), although the EMP examination revealed only one grain of the natural dumortierite studied here to have a very low boron surplus (up to 0.03 [4]B). Neither Raman spectroscopic study nor EMP analysis detected [4]B in tourmaline. The findings of dumortierite and tourmaline in the diamondiferous gneisses provide important implications for the presence of a boron‐rich fluid or melt during subduction/exhumation processes.