Abstract

Research subject. The chemical composition and spectroscopic properties of almandine jewelry garnets from the Kite-lya deposit in the Northern Ladoga region (Karelia). Materials and methods. The chemical composition, impurity elements, mineral inclusions and spectroscopic properties of almandine jewelry crystals were studied using IR and Mössbauer spectroscopy. Results. Garnet crystals were found to exhibit a weakly pronounced zonal composition, varying from Alm75Pir15Sps7Grs3 in the center to Alm80Pir14Sps4Grs2 at their edges. Therefore, the Ca and Mn contents decrease towards the grain edges. This zonality of garnets is characteristic of the processes of progressive metamorphism of their host rocks. The garnet crystals feature small inclusions of quartz, chlorite, mica FACI (biotite), ilmenite, rutile, monazite, zircon and pyrrhotite. The composition of chlorite, biotite and zircon was established. The parameter of the cube unit cell ao = 11.522 ± 0.003 Å was calculated. The IR absorption spectra of 995, 966, 901, 878, 638, 568, 528, 476 and 455 cm–1 are characteristic of the pyrope-almandine difference. Mössbauer spectroscopy revealed an insignificant admixture of trivalent iron (Fe3+) in the structure of Kitelya garnets (≈1 % of the amount of isomorphic iron). The obtained optical absorption spectra of garnet plates in the visible light spectrum indicate that Fe2+ ions in dodecahedral positions, to a lesser extent dodecahedral Mn2+ ions, as well as possibly octahedral Fe3+ ions are responsible for the bright red-crimson color of pyrop-almandine from the Kitelya deposit. Conclusions. A “portrait” of typomorphic features (composition and properties) of the pyrope-almandine jewelry garnet from the Kitelya deposit was obtained. This portrait can be used when analyzing the historical finds of faceted or cabochonized differences of almandine in jewelry, church utensils in both Russia and Europe (where this jewelry material was exported during the 17th century). The preservation of garnet jewelry differences in the host rock is due to the presence of thin amorphous kelefite shells or soft minerals (sericite, chlorite, kaolinite etc.).

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