The garnet supergroup includes all minerals isostructural with garnet regardless of what elements occupy the four atomic sites, i.e., the supergroup includes several chemical classes. There are presently 32 approved species, with an additional 5 possible species needing further study to be approved. The general formula for the garnet supergroup minerals is {X₃}[Y₂](Z₃)ϕ₁₂, where X, Y, and Z refer to dodecahedral, octahedral, and tetrahedral sites, respectively, and ϕ is O, OH, or F. Most garnets are cubic, space group Ia3̄d (no. 230), but two OH-bearing species (henritermierite and holtstamite) have tetragonal symmetry, space group, I4₁/acd (no. 142), and their X, Z, and ϕ sites are split into more symmetrically unique atomic positions. Total charge at the Z site and symmetry are criteria for distinguishing groups, whereas the dominant-constituent and dominant-valency rules are critical in identifying species. Twenty-nine species belong to one of five groups: the tetragonal henritermierite group and the isometric bitikleite, schorlomite, garnet, and berzeliite groups with a total charge at Z of 8 (silicate), 9 (oxide), 10 (silicate), 12 (silicate), and 15 (vanadate, arsenate), respectively. Three species are single representatives of potential groups in which Z is vacant or occupied by monovalent (halide, hydroxide) or divalent cations (oxide). We recommend that suffixes (other than Levinson modifiers) not be used in naming minerals in the garnet supergroup. Existing names with suffixes have been replaced with new root names where necessary: bitikleite-(SnAl) to bitikleite, bitikleite-(SnFe) to dzhuluite, bitikleite-(ZrFe) to usturite, and elbrusite-(Zr) to elbrusite. The name hibschite has been discredited in favor of grossular as Si is the dominant cation at the Z site. Twenty-one end-members have been reported as subordinate components in minerals of the garnet supergroup of which six have been reported in amounts up to 20 mol% or more, and, thus, there is potential for more species to be discovered in the garnet supergroup. The nomenclature outlined in this report has been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (Voting Proposal 11-D).

Harmunite, naturally occurring calcium ferrite CaFe₂O₄, was discovered in the Hatrurim Complex of pyrometamorphic larnite rocks close to the Jabel Harmun, the Judean Desert, West Bank, Palestinian Autonomy, Israel. The new mineral occurs in larnite pebbles of the pseudo-conglomerate, the cement of which consists of intensely altered larnite-bearing rocks. Srebrodolskite, magnesioferrite, and harmunite are intergrown forming black porous aggregates to the central part of the pebbles. Larnite, fluorellestadite, ye’elimite, fluormayenite, gehlenite, ternesite, and calciolangbeinite are the main associated minerals. Empirical crystal chemical formula of harmunite from type specimen is as follows Ca_1.013(Fe³⁺_1.957Al_0.015Cr³⁺_0.011Ti⁴⁺_0.004 Mg_0.003)_∑1.993O₄. Calculated density is 4.404 g/cm³, microhardness VHN₅₀ is 655 kg/mm². The Raman spectrum of harmunite is similar to that of the synthetic analog. Harmunite in hand specimen is black and under reflected plane-polarized light is light gray with red internal reflections. Reflectance data for the COM wavelengths vary from ~22% (400 nm) to ~18% (700 nm). The crystal structure of harmunite [Pnma; a = 9.2183(3), b = 3.0175(1), c = 10.6934(4) Å; Z = 4, V = 297.45(2) ų], analogous to the synthetic counterpart, was refined from X-ray single-crystal data to R1 = 0.0262. The structure of CaFe₂O₄ consist of two symmetrically independent FeO₆ octahedra connected over common edges, forming double rutile-type _∞¹[Fe₂O₆] chains. Four such double chains are further linked by common oxygen corners creating a tunnel-structure with large trigonal prismatic cavities occupied by Ca along [001]. The strongest diffraction lines are as follows [d_hkl, (I)]: 2.6632 (100), 2.5244 (60), 2.6697 (52), 1.8335 (40), 2.5225 (35), 2.2318 (34), 1.8307 (27), 1.5098 (19). Crystallization of harmunite takes place in the presence of sulfate melt.

Lakargiite CaZrO₃ –– the zirconium analog of perovskite [Pbnm, a = 5.556(1), b = 5.715(1), c = 7.960(1) Å, V 252.7(1) ų, Z = 4] was discovered as an accessory mineral in high-temperature skarns in carbonate-silicate rocks occurring as xenoliths in ignimbrites of the Upper-Chegem (Verkhniy Chegem) volcanic structure, the North Caucasus, Kabardino-Balkaria, Russia. Lakargiite forms pseudo-cubic crystals up to 30 35 μm in size and aggregates up to 200 μm. Lakargiite is associated with spurrite, larnite, calcio-olivine, calcite, cuspidine, rondorfite, reinhardbraunsite, wadalite, perovskite, and minerals of the ellestadite group. The new perovskite mineral belongs to the ternary solid solution CaZrO₃-CaTiO₃-CaSnO₃ with a maximum CaZrO₃ content of ca. 93%, maximum CaTiO₃ content of 22%, and maximum CaSnO₃ content of 20%. Significant impurities are Sc, Cr, Fe, Ce, La, Hf, Nb, U, and Th. Raman spectra of lakargiite are similar to those of the synthetic phase Ca(Zr,Ti)O₃ with strong bands at 352, 437, 446, 554, and 748 cm⁻¹. Lakargiite crystallized under sanidinite-facies conditions of contact metamorphism characterized by very high temperatures and low pressures.