Xenotime-(Gd), ideally GdPO4, is a new mineral of the xenotime group. It was discovered at the Zimná Voda REE–U–Au occurrence near Prakovce, Western Carpathians, Slovakia. It forms rare crystal domains (≤20 μm, usually ≤10 μm in size) in Gd-rich xenotime-(Y) crystals (≤100 μm in size), in association with monazite-group minerals, uraninite, fluorapatite and uranyl arsenates–phosphates. The hydrothermal REE–U–Au mineralisation occurs in a quartz–muscovite vein, hosted in Palaeozoic phyllites near exocontact with Permian granites. The density is 5.26 g/cm3, based on calculated average empirical formula and unit-cell parameters. The average chemical composition (n = 6) measured by electron microprobe is as follows (wt.%): P2O5 30.1, As2O5 0.5, SiO2 0.2, UO2 0.3, Y2O3 15.7, (La, Ce, Pr, Nd)2O3 0.5, Sm2O3 5.7, Eu2O3 1.4, Gd2O3 29.2, Tb2O3 3.9, Dy2O3 10.4, Ho2O3 0.4, (Er, Tm, Yb, Lu)2O3 2.1, (Ca, Fe, Pb, Mn, Ba)O 0.1, total 100.5. The corresponding empirical formula calculated on the basis of 4 oxygen atoms is: (Gd0.37Y0.32Dy0.13Sm0.08Tb0.05Eu0.02Er0.01Tm0.01Nd0.01…)Σ1.01(P0.98As0.01Si0.01)O4. The empirical formula of the Gd-richest composition is: (Gd0.38Y0.31Dy0.13Sm0.08Tb0.05Eu0.02Er0.01Nd0.01Ho0.01…)Σ1.01(P0.98As0.01Si0.01)O4. The ideal formula is GdPO4. The xenotime-type structure has been confirmed by micro-Raman spectroscopy and a Fast Fourier-Transform pattern using HRTEM. Xenotime-(Gd) is tetragonal, space group I41/amd, a = 6.9589(5) Å, c = 6.0518(6) Å, V = 293.07(3) Å3 and Z = 4. The new mineral is named as an analogue of xenotime-(Y) and xenotime-(Yb) with Gd dominant among the REE. The middle REE enrichment of xenotime-(Gd) is shared with the associated monazite-(Gd) and Gd-rich hingganite-(Y). This exotic REE signature and precipitation of Gd-bearing minerals is a product of selective complexing and enrichment in MREE in low-temperature hydrothermal fluids by alteration of uraninite, brannerite and fluorapatite on a micro-scale. The existence of xenotime-(Gd) and monazite-(Gd) is the first naturally documented dimorphism among REE phosphates. In addition, xenotime-(Gd) is only the third approved Gd-dominant mineral, after lepersonnite-(Gd) and monazite-(Gd).

Rundqvistite-(Ce), ideally Na3(Sr3Ce)(Zn2Si8O24), is a new mineral from the Darai-Pioz alkaline massif, Tien-Shan Mountains, Tajikistan. The mineral occurs as elongated grains up to 0.1 mm long and up to 0.03 mm thick embedded in quartz–pectolite aggregate in a silexite-like peralkaline pegmatite. Associated minerals are quartz, fluorite, pectolite, baratovite, aegirine, leucosphenite, neptunite, reedmergnerite, orlovite, sokolovaite, mendeleevite-(Ce), odigitriaite, pekovite, zeravshanite, kirchhoffite and garmite. The mineral is colourless with a vitreous lustre and a white streak, brittle, Dmeas. is 3.70(2) and Dcalc. is 3.709 g/cm3. Rundqvistite-(Ce) is monoclinic, space group P21/c, a = 5.1934(16), b = 7.8934(16), c = 26.011(5) Å, β = 90.02(3)° and V = 1066.3(4) Å3. The chemical composition of rundqvistite-(Ce) is SiO2 40.17, La2O3 2.64, Ce2O3 7.55, Pr2O3 0.80, Nd2O3 2.43, Sm2O3 0.33, Eu2O3 0.09, Gd2O3 0.24, Tb2O3 0.18, Dy2O3 0.21, PbO 1.03, SrO 19.83, FeO 0.37, ZnO 13.08, CaO 2.55, Na2O 8.04, total 99.54 wt.%. The empirical formula calculated on 24 O apfu (atoms per formula unit) is Na3.10Sr2.29Ca0.54Pb0.06(Ce0.55La0.19Nd0.17Pr0.06Sm0.02Gd0.02Eu0.01Tb0.01Dy0.01)Σ1.04Zn1.92Fe0.06 Si8.00O24 Z = 2. The structural formula based on refined site-occupancies is (Na2.94Sr0.06)Σ3.00 [(Sr2.23Ca0.54Pb0.06Na0.13)Σ2.96Ln3+1.04]Σ4.00[(Zn1.92Fe2+0.06)Σ1.98Si8O24], where Ln3+1.04 = (Ce0.55La0.19Nd0.17Pr0.06Sm0.02Gd0.02Eu0.01Tb0.01Dy0.01)Σ1.04. The crystal structure of rundqvistite-(Ce) was refined to R1 = 2.76% on the basis of 3184 unique reflections [F > 4σ|F|]. In rundqvistite-(Ce), the main structural unit is a (Zn2Si8O24)12– sheet parallel to (100). In the sheet, the Si and Zn tetrahedra form four-, five- and eight-membered rings. The interstitial cations at the Na and M(1–3) sites sum to [Na3(Sr3Ce)]12– apfu. The Na and M(1–3) polyhedra share common edges to form a layer. Rundqvistite-(Ce) is a structural analogue of vladykinite, ideally Na3Sr4(Fe2+Fe3+)Si8O24. Rundqvistite-(Ce) and vladykinite are related by the following substitution: [8]Ce3+ + [4](Zn2+)2 ↔ [8]Sr2+ + [4](Fe2+Fe3+). The mineral is named after Dmitry Vasilievich Rundqvist (1930–2022), a prominent Russian geologist and an expert on the geology of ore deposits, metallogeny and mineralogy of Precambrian rocks.

Hakite-(Cd), hakite-(Fe) and hakite-(Zn) are new minerals belonging to the tetrahedrite group and forming, along with hakite-(Hg), the hakite series. They have been discovered in samples collected from the Bytíz deposit, in the uranium and base-metal Příbram ore district, Central Bohemia, Czech Republic. They occur as anhedral grains, up to 300 μm in size, in a calcite gangue, associated with clausthalite, cadmoselite, hakite-(Hg) [for hakite-(Cd)], berzelianite, bukovite, bytízite, crookesite, chaméanite, eskebornite, příbramite, the not yet approved giraudite-(Hg) and giraudite-(Cu), hakite-(Hg), umangite, chalcopyrite, tetrahedrite-(Zn) and a new Cu–As selenide [for hakite-(Fe) and -(Zn)]. The three new species are black, with a metallic lustre. Mohs hardness is ca. 3½–4; calculated density is 6.019 (Hak-Cd), 6.011 (Hak-Fe) and 6.081 g.cm–3 (Hak-Zn). In reflected light, they are isotropic, pale grey with bluish (Hak-Cd) or brownish (Hak-Fe and Hak-Zn) shades. Empirical formulae of hakite-(Cd), hakite-(Fe), and hakite-(Zn) are Cu9.71Ag0.24Cd1.51Hg0.43Zn0.03(Sb3.94As0.13)Σ4.07Se11.35S1.57, Cu10.11Ag0.18Fe0.81Zn0.50Hg0.26(Sb3.72As0.41)Σ4.13Se12.65S0.12, and Cu10.03Ag0.24Zn0.61Fe0.53Hg0.45(Sb3.55As0.60)Σ4.15Se12.82S0.08, respectively. These formulae correspond to the end-member formulae Cu6(Cu4Cd2)Sb4Se13 (Hak-Cd), Cu6(Cu4Fe2)Sb4Se13 (Hak-Fe), and Cu6(Cu4Zn2)Sb4Se13 (Hak-Zn). All these new members of the hakite series are cubic, I$\bar{4}$3m, Z = 2, with unit-cell parameters a = 10.8860(6) Å, V = 1290.0(2) Å3 (Hak-Cd); a = 10.7983(4) Å, V = 1259.12(14) Å3 (Hak-Fe); and a = 10.8116(14) Å, V = 1263.8(5) Å3 (Hak-Zn). These species are isotypic with the other members of the tetrahedrite group, and their crystal structures have been refined on the basis of single-crystal X-ray diffraction data down to R1 values of 0.0230 (Hak-Cd), 0.0254 (Hak-Fe), and 0.0302 (Hak-Zn). These structural data allow us to describe the S-to-Se partitioning in hakite-series minerals and to understand the mechanisms avoiding too short Me–Se distances in these selenides.

Clogauite, ideally PbBi4Te4S3 is the new n = 1 member of the aleksite series, PbnBi4Te4Sn+2, where n is the homologue number. Clogauite is named from the type locality, the Clogau gold mine, Dolgellau Gold belt, Gwynedd, North Wales, United Kingdom. The mineral and name have been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA2023–062). The aleksite series is an accretional homologous series in which each member is derived from the same 5-atom tetradymite archetype. Clogauite crystallises in the trigonal crystal system (space group: P$\bar{3}$m1, #164). Three distinct polytypes of clogauite are recognised, corresponding to identical chemistry but different layer sequences, expressed as (57), (5559) and (557.559), respectively, in reference to the number of atoms in individual layer sequences. These are clogauite-12H, a = 4.277(4) Å, c = 23.46(14) Å, V = 371.598 Å3 and Z = 1; clogauite-24H, a = 4.278(4) Å, c = 46.88(31) Å, V = 743.053 Å3 and Z = 2; and clogauite-36H, a = 4.278(4) Å, c = 70.36(32) Å, V = 1115.283 Å3 and Z = 3. Clogauite is opaque, with a pale grey colour in reflected light. Reflectance is higher than tetradymite or galena. Bireflectance and anisotropy are strong. Structural data were determined from measurement of atomic-scale HAADF STEM imaging showing the internal arrangement of component atoms and characteristic selected area electron diffraction patterns for each polytype. The structures were then further constrained from ab initio total energy calculations and structure relaxation using density functional theory (DFT) using the measured parameters as input data. The relaxed crystal structure for each polytype was modelled to generate crystallographic information files (cif). STEM and electron diffraction simulations based on the crystallographic information data obtained from the DFT calculations show an excellent match to the empirical measurements.

Markwelchite, ideally TlPbSbS3, is a new mineral from the hydrothermal deposit of Jas Roux, Hautes-Alpes, France. It occurs as a black anhedral crystal associated closely with protochabournéite. Microhardness measurements (VHN15) gave a mean value of 197 kg/mm2 corresponding to a Mohs hardness of ~3–4. In plane-polarised incident light, markwelchite is grey in colour. Under crossed polars, it is distinctly anisotropic with greyish white to bluish rotation tints, with bright red internal reflections. Reflectance percentages (Rmin and Rmax) are: 28.5, 31.5 (471.1 nm); 28.3, 30.7 (548.3 nm); 27.9, 30.3 (586.6 nm); and 27.6, 29.8 (652.3 nm). The mean of 5 electron microprobe spot analyses gave Tl 34.67(45), Pb 31.86(25), Sb 15.06(15), As 2.37(5), S 15.35(20), total 99.31 wt.%, corresponding, on the basis of a total of 6 atoms per formula unit and structural results, to Tl1.063Pb0.964(Sb0.775As0.198)Σ0.973S3.000. Single-crystal X-ray diffraction studies revealed that markwelchite is isotypic with richardsollyite, TlPbAsS3. It is monoclinic, space group P21/c, with the following unit-cell parameters: a = 8.9144(3), b = 8.4513(3), c = 8.6511(3) Å, β = 108.723(4)°, V = 617.27(4) Å3 and Z = 4. The five strongest observed powder-diffraction lines [d in Å (Irel)(hkl)] are: 3.88 (100)($\bar{2}$11); 3.78 (90)(210); 3.29 (90)(102); 2.73 (85)($\bar{1}$13); and 2.93 (75)(022). The crystal structure can be described as formed by (100) [Me2(SbS3)]– layers sandwiching the Me1+ cations. The Me1 site has a seven-fold coordination, whereas the Me2 site has an 6+2 coordination corresponding to a distorted, bicapped trigonal prismatic coordination, and the Sb site displays a trigonal pyramidal coordination with three S atoms and Sb at the apex.

The name markwelchite honours Dr Mark D. Welch of the Natural History Museum, London, UK.

The new mineral has been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA2024–001). A discussion on the relationships between markwelchite and synthetic TlPbSbS3 is also provided.

The new mineral theuerdankite, ideally Ag3AsO4, was found in the Alter Theuerdank Mine, Beerberg, St. Andreasberg, Goslar District, Lower Saxony, Germany. Theuerdankite occurs as aggregates of anhedral grains up to 3 mm in size, growing in cavities of strongly supergene-weathered material consisting of native silver and chlorargyrite (but with calcite present). It is dark violet, changing to reddish and black when exposed to the air and light. It has a grey to violet grey streak; when readily fresh, its streak is brownish-red. The Mohs hardness is ~2. It is brittle with no observable cleavage or parting and with a conchoidal fracture. The calculated density is 6.620 g⋅cm–3. In reflected light, theuerdankite is dark grey with a pinkish tint, with no observable bireflectance, pleochroism, or anisotropy. It shows dark red internal reflections. The reflectance values for wavelengths recommended by the Commission on Ore Mineralogy of the International Mineralogical Association are (R, %): 13.3 (470 nm), 12.8 (546 nm), 12.7 (589 nm) and 12.5 (650 nm). The empirical formula (based on 4 apfu) is Ag3.00As1.00O4. Theuerdankite is cubic, space group P$\bar{4}$3n, a = 6.144(2) Å, V = 231.93(13) Å3 and Z = 2. The six strongest powder X-ray diffraction lines are [dobs in Å, (I) hkl]: 3.0736, (22) 200; 2.7502, (100) 210; 2.5106, (55) 211; 1.7050, (36) 320; 1.6249, (44) 321; and 1.3412, (17) 421. The crystal structure of theuerdankite (R1 = 1.69% for 519 reflections having I > 3σ(I)), is isotypic to those of synthetic Ag3AsO4 and Ag3PO4. The Gram–Charlier development describing the higher-order tensors representing the atomic displacement parameters of the silver atom was implemented, documenting that silver tends to behave anharmonically in the theuerdankite structure at room temperature.

Sperlingite, (H2O)K(Mn2+Fe3+)(Al2Ti)(PO4)4[O(OH)][(H2O)9(OH)]⋅4H2O, is a new monoclinic member of the paulkerrite group, from the Hagendorf-Süd pegmatite, Oberpfalz, Bavaria, Germany. It was found in corrosion pits of altered zwieselite, in association with columbite, hopeite, leucophosphite, mitridatite, scholzite, orange–brown zincoberaunite sprays and tiny green crystals of zincolibethenite. Sperlingite forms colourless prisms with pyramidal terminations, which are predominantly only 5 to 20 μm in size, rarely to 60 μm and frequently are multiply intergrown and are overgrown with smaller crystals. The crystals are flattened on {010} and slightly elongated along [100] with forms {010}, {001} and {111}. Twinning occurs by rotation about c. The calculated density is 2.40 g⋅cm–3. Optically, sperlingite crystals are biaxial (+), α = 1.600(est), β = 1.615(5), γ = 1.635(5) (white light) and 2V (calc.) = 82.7°. The optical orientation is X = b, Y = c and Z = a. Neither dispersion nor pleochroism were observed. The empirical formula from electron microprobe analyses and structure refinement is A1[(H2O)0.96K0.04]Σ1.00 A2(K0.52□0.48)Σ1.00 M1(Mn2+0.60Mg0.33Zn0.29Fe3+0.77)Σ1.99 M2+M3(Al1.05Ti4+1.33Fe3+0.62)Σ3.00(PO4)4 X[F0.19(OH)0.94O0.87]Σ2.00[(H2O)9.23(OH)0.77]Σ10.00⋅3.96H2O. Sperlingite has monoclinic symmetry with space group P21/c and unit-cell parameters a = 10.428(2) Å, b = 20.281(4) Å, c = 12.223(2) Å, β = 90.10(3)°, V = 2585.0(8) Å3 and Z = 4. The crystal structure was refined using synchrotron single-crystal data to wRobs = 0.058 for 5608 reflections with I > 3σ(I). Sperlingite is the first paulkerrite-group mineral to have co-dominant divalent and trivalent cations at the M1 sites; All other reported members have Mn2+ or Mg dominant at M1. Local charge balance for Fe3+ at M1 is achieved by H2O → OH– at H2O coordinated to M1.

The new ludwigite-group mineral savelievaite, ideally Mg2Cr3+O2(BO3), was found in the chromitite body at the Malaya Kharamatalou river valley, Voikar–Syninskiy ultrabasic complex, Polar Urals, Russia. Savelievaite and Cr-enriched ludwigite occur in clinochlore veinlets and are associated with earlier magnesiochromite, spinel, chromite, pargasite, diopside, forsterite, serpentine, magnetite and pentlandite. Savelievaite forms prismatic, acicular or fibrous crystals up to 0.05 × 0.4 mm, usually assembled in radiating or chaotic clusters up to 1 × 1.5 mm across. It is opaque, black to greenish-black. The lustre is vitreous for prismatic crystals and silky for fibrous aggregates. D(calc.) = 3.91 g cm–3. Under the microscope in reflected light, savelievaite is grey, non-pleochroic, with weak bireflectance and anisotropism. The chemical composition (wt.%, EMPA, Fe2+:Fe3+ ratio by stoichiometry) is: MgO 34.88, FeO 10.83, NiO 0.36, B2O3 16.80, Al2O3 2.97, V2O3 0.21, Cr2O3 21.97, Fe2O3 12.40, TiO2 0.43, total 100.85. The empirical formula calculated on the basis of 5 O apfu is (Mg1.72Fe2+0.30Ni0.01)Σ2.03(Cr3+0.57Fe3+0.31Al0.12Ti0.01V3+0.01)Σ1.02B0.96O5. Savelievaite is orthorhombic, space group Pbam, a = 9.2631(6), b = 12.2298(8), c = 3.0104(2) Å, V = 341.04(4) Å3 and Z = 4. The strongest reflections of the powder X-ray diffraction pattern [d,Å(I)(hkl)] are: 5.101(100)(120); 2.551(90)(240); 2.524(88)(201); 2.163(36)(250); and 2.033(55)(321). The crystal structure was solved from single-crystal X-ray diffraction data and refined to R1 = 0.0405. Savelievaite is isostructural with ludwigite, Cr3+ is concentrated at the M4 site. The mineral is named in honour of the Russian petrologist and geologist Dr. Galina Nikolaevna Savelieva (b. 1936). Ludwigite, ideally Mg2Fe3+O2(BO3), and savelievaite form a continuous isomorphous series in which Cr3+ content varies from 0 to 0.60 apfu. Occurrences of Cr-enriched (>1 wt.% Cr2O3) varieties of ludwigite are mainly related to ultrabasic complexes. The Cr-richest (>10 wt.% Cr2O3) ludwigite–savelievaite-series members are found in chromite ores at the Voikar–Syninskiy complex and Volchiegorskoe and Tatishchevskoe deposits, both in the South Urals.

Zipserite is a new mineral species discovered in a sample collected from the old mine dumps of the abandoned epithermal deposit Nagybörzsöny in Hungary. Zipserite occurs as anhedral to subhedral, lath-like grains, up to 500 μm in size, in hydrothermally strongly altered rocks. It is found at a contact between bismuth and bismuthinite, also associated with rare ikunolite and joséite-A. Zipserite is silvery white with a metallic lustre. Mohs hardness is ca. 2–3 and the calculated density is 7.815 g.cm–3. In reflected light, zipserite is grey–white, with colour and reflectance essentially matching those of bismuthinite. Bireflectance is weak, internal reflections not present. Anisotropy is moderately strong, with dark blue and grey colours of anisotropy. Reflectance values for the four Commission on Ore Mineralogy wavelengths of zipserite in air [Rmax, Rmin (%) (λ in nm)] are: 48.4, 46.4 (470); 47.8, 45.9 (546); 47.8, 45.8 (589); and 47.5, 45.6 (650). The empirical formula, based on electron-microprobe analyses, is (Bi4.74Pb0.31)Σ5.05(S3.38Se0.56Te0.02)Σ3.96, that can be simplified as Bi5(S,Se)4. The ideal end-member formula of zipserite is Bi5S4, which requires Bi 89.07 and S 10.93, total 100 wt.%. Zipserite possesses a fascinating crystal structure. The average structure is trigonal, with space group P$\bar{3}$m, a = 4.162(1) Å, c = 16.397(1) Å, V = 245.94(4) Å3 and Z = 2. The structure is built by the alternation of a double bismuth layer Bi2 and the Bi3S4 block which is a three octahedra thick layer. Its general formula can be expressed as Bi2 + Bi3S4, which corresponds directly to the observed stacking. At 98 K, the structure can be described using the superspace formalism with an R-centred trigonal unit cell a = 4.209(2) Å, c0 = 5.616(6) Å, a modulation vector q ≈ 4/3 c* and the superspace group R$\bar{3}$m(00γ)00. Zipserite is not only a new mineral but also the first named member of a new sub-group of compounds within the broader family of bismuth chalcogenides, characterised by complex stacking of structural units (Bi2 layers and Bi3S4 blocks). Some of these phases are being investigated as promising thermoelectric materials and synthetic analogues of zipserite could also be inspected for similar physical properties.

Qeltite (IMA2021–032), ideally Ca3Ti(Fe2Si)Si2O14, was found in gehlenite–rankinite–wollastonite paralava from a pyrometamorphic rock of the Hatrurim Complex at Nabi Musa locality, Judean Desert, West Bank, Palestine. It generally occurs as light-brown flattened crystals up to 40–50 μm in length and less than 5 μm in thickness. Its aggregates reach 100–200 μm in size. Its empirical crystal chemical formula based on 14 O is: (Ca2.96Sr0.02Mn0.01)Σ2.99Ti4+(Fe3+1.59Si0.60Al0.43Ti4+0.38Cr0.01)Σ3.01(Si1.99P0.01)Σ2O14. The strongest reflections in its calculated X-ray diffraction pattern are [d, Å, (I, %), hkl]: 3.12, (100), 111; 2.85, (61), 201; 2.85, (48), 021; 2.32, (45), 211; 6.93, (31), 100; and 1.81, (30), 212. Qeltite is trigonal and crystallises in the noncentrosymmetric P321 space group, with a = 8.0077(5) Å, c = 4.9956(4) Å, V = 277.42(4) Å3 and Z = 1. Its microhardness VHN25 is 708(17) kg/mm2 and its hardness on the Mohs scale is ~6. Its calculated density is 3.48 g/cm3. It was found in fine-grained mineral aggregates within coarse-grained main minerals of rankinite–gehlenite paralava with subordinate wollastonite, Ti-bearing andradite and kalsilite. In these aggregates, the mineral is associated with khesinite, paqueite and pseudowollastonite, indicating a high-temperature genesis (~1200°C). Its crystallisation can be compared with the crystallisation of minerals containing refractory inclusions in meteorites.

Kvačekite is a new mineral species discovered in a sample collected from the now abandoned Bukov uranium mine, western Moravia, Czech Republic. It occurs as rare anhedral grains, up to 15 μm in size, associated with nickeltyrrellite, tyrrellite, berzelianite, hakite-(Zn), hakite-(Cd), eucairite, clausthalite, and gold in calcite gangue. In reflected light, kvačekite is white with a faint yellowish shade; bireflectance, pleochroism and anisotropy are absent. Internal reflections were not observed. Reflectance values for the four COM wavelengths for kvačekite in air [R (%) (λ in nm)] are: 54.9 (470); 53.5 (546); 52.6 (589); and 52.2 (650). The empirical formula, based on electron-microprobe analyses (EPMA), is (Ni0.95Cu0.04Co0.03)Σ1.02Sb1.00(Se0.97S0.01)Σ0.98. The ideal formula is NiSbSe, which requires (in wt.%) Ni 22.63, Sb 46.93, Se 30.44, total 100.00. Kvačekite is cubic, P213, with unit-cell parameters a = 6.09013(13) Å, V = 225.881(15) Å3 and Z = 4. The strongest reflections in the X-ray powder diffraction pattern of synthetic kvačekite [d, Å (I) hkl] are: 3.0458 (11) 200; 2.7242 (100) 201, 210; 2.4867 (71) 211; 1.8632(39) 311; 1.6277(29) 321, 312; and 1.3290 (13) 421. Given the similarity with ullmannite, NiSbS, the crystal structure was refined from the powder X-ray diffraction data starting from those atomic coordinates using the synthetic analogue of kvačekite. Its crystal structure is formed by corner-sharing [NiSb3Se3] octahedra which form a three-dimensional network. The identity of the natural kvačekite and synthetic cubic NiSbSe were confirmed by a study of their chemical composition, reflectance measurements, Raman spectroscopy and electron back-scattered diffraction (EBSD) measurements on the mineral. Kvačekite is named after Milan Kvaček (1930–1993), a prominent Czech mineralogist. The mineral and its name have been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA2023-095).

Ermeloite is a new aluminium phosphate mineral from Galicia, Spain, in the northwest of the Iberian Peninsula. It is the third formally recognised mineral discovered in Galicia since morenosite and cervantite in the 19th Century. The name and symbol (Erm) were approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA2021–017a) in recognition of the geographical location where it was found. The mineral occurs as a light blue to white fine aggregate over quartz and microcline associated with wardite. Crystals of ~0.04 mm are transparent and have a waxy lustre. The simplified empirical formula determined using electron microprobe analysis is Al1.02P0.95F0.06O3.88⋅1.06 H2O, which is near to the ideal formula Al(PO4)⋅H2O. The mineral is an alteration product within a phosphate pegmatite. Ermeloite is the second phosphate isostructural with the sulfates of the kieserite group. Single-crystal X-ray diffraction showed that ermeloite crystallises in the monoclinic C2/c space group with cell parameters a = 6.5371(4) Å, b = 7.5670(5) Å, c = 7.1146(5) Å, β = 115.335(2)°, V = 318.08(4) Å3 and Z = 4 at room temperature. Comparative analysis of the crystallographic data, with isostructural phosphates, revealed an interesting behaviour for these compounds.

Gorerite, ideally CaAlFe11O19 is a new mineral and M-type hexaferrite of the magnetoplumbite group. It was found in ferrite-rich segregations of esseneite–gehlenite–wollastonite–anorthite melted rock of the ‘olive’ subunit of pyrometamorphic rocks located near Hatrurim Junction in the Negev Desert, Israel. Within these ferrite-rich segregations up to 100 μm in size, platy crystals of gorerite up to 50 μm in size intergrow with hibonite, hematite, maghemite, magnesioferrite, dorrite, barioferrite and andradite, forming aggregates. Additionally, small crystals of gorerite occur within magnesioferrite. Importantly, gorerite did not crystallise directly from the melt. Instead, it emerged through a reaction involving earlier crystallised hibonite and an iron-enriched melt, resulting in the partial or complete replacement of hibonite by gorerite. Gorerite appears grey in the reflected light (R = 18–23%), displaying distinct bireflectance: dark-grey perpendicular to Z and light-grey parallel to Z. Its Raman spectrum exhibits only one strong band at 700 cm–1, which shifts to higher frequencies with increasing Al content. Gorerite crystallises in the P63/mmc space group, with lattice parameters a = 5.8532(4) Å, c = 22.7730(2) Å and V = 675.67(7) Å3 with Z = 2. It exhibits a structure characterised by an intercalation of triple spinel-like S blocks and rock-salt type R blocks along the hexagonal c-axis.

The new eudialyte-group mineral amableite-(Ce), ideally Na15[(Ce1.5Na1.5)Mn3]Mn2Zr3□Si[Si24O69(OH)3](OH)2⋅H2O, was discovered in a peralkaline pegmatite at Saint-Amable Sill, Montérégie, Québec, Canada. The associated minerals are albite, microcline, aegirine, serandite, natrolite, yofortierite, and an unidentified titanosilicate forming minute grains. Amableite-(Ce) occurs as yellow equant or thick tabular crystals up to 2 mm across. The observed crystal forms are {0001}; the subordinate forms are {11$\bar{2}$0}, {10$\bar{1}$1}, and {10$\bar{1}$0}. Amableite-(Ce) is brittle, with a Mohs hardness of 5. D(meas) = 2.89(1), D(calc) = 2.899 g⋅cm–3. Amableite-(Ce) is optically anomalously biaxial (+) with α ≈ β = 1.603(2) and γ = 1.608(2). The chemical composition is (wt.%, electron microprobe, H2O measured by means of a modified Penfield method): Na2O 14.20, K2O 0.41, CaO 1.89, MnO 8.25, Fe2O3 2.40, La2O3 3.10, Ce2O3 4.19, Pr2O3 0.16, Nd2O3 0.59, SiO2 49.41, ZrO2 11.17, HfO2 0.24, TiO2 0.68, Nb2О5 1.54, Cl 0.26, H2O 1.70, –O≡Cl –0.06, total 100.13. The crystal structure was determined using single-crystal X-ray diffraction data and refined to R1 = 0.0423. Amableite-(Ce) is trigonal, space group R3, with a = 14.1340(3) Å, c = 30.3780(11) Å and V = 5255.6(3) Å3. The crystal-chemical formula is (Na12.93K0.27Ce0.06)Σ13.26[(Mn2.49Ce0.30Ca0.21)Σ3.00(Ce1.14Na1.04Ca0.82)Σ3.00](Mn1.05Fe0.90□1.05)Σ3.00(Zr2.85Ti0.12Hf0.03)Σ3.00(□0.40Nb0.36Si0.24)Σ1.00(Si0.88□0.12)Σ1.00[Si24(O70.44(OH)1.56)Σ72.00][(OH)2.20(H2O)1.27]Σ3.47Cl0.22 (Z = 3). Infrared and Raman spectra are given. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %)(hkl)] are: 11.34 (51)(101), 7.06 (76)(110), 4.312 (63)(205), 3.783 (38)(033), 3.538 (43)(027, 220), 2.963 (84)($\bar{3}$45), 2.837 (100)(404). The mineral is named after the discovery locality.

Tetrahedrite-(Cu), Cu12Sb4S13, has been approved as a new mineral species (IMA2022–078) from the Bankov magnesite deposit near Košice, Slovak Republic where it occurs as anhedral grains, up to 0.4 mm across, associated with skinnerite, chalcostibite, famatinite, tetrahedrite-(Fe) and zoned aggregates of tennantite-(Cu) to tennantite-(Fe). Tetrahedrite-(Cu) is steel-grey, with a metallic lustre. Mohs hardness is ca. 3½–4 and calculated density is 5.029 g.cm–3. In reflected light, tetrahedrite-(Cu) is isotropic and grey with a bluish shade. Reflectance data for the four COM wavelengths in air are [λ (nm): R (%)]: 470: 31.1; 546: 30.1; 589: 29.9; and 650: 28.1. The empirical formula, based on electron-microprobe data (mean of 17 spot analyses), is Cu11.42Zn0.26Fe0.19(Sb4.06As0.08)Σ4.14S12.99. The ideal formula is Cu6(Cu4Cu2)Sb4S13, which requires (in wt.%) Cu 45.76, Sb 29.23 and S 25.01, total 100.00. Tetrahedrite-(Cu) is cubic, I$\bar{4}$3m, with unit-cell parameters a = 10.3296(15) Å, V = 1102.2(5) Å3 and Z = 2. Its crystal structure was refined by single-crystal X-ray diffraction data to a final R1 = 0.0347 on the basis of 261 unique reflections with Fo > 4σ(Fo) and 22 refined parameters. Tetrahedrite-(Cu) is isotypic with other tetrahedrite-group minerals. Previous findings of tetrahedrite-(Cu) are reported and some nomenclature issues, related to the Fe and Cu oxidation states, are discussed. At the Bankov deposit, tetrahedrite-(Cu) is related to hydrothermal, most probably Alpine, solutions strongly enriched in Cu, Sb and S.

The new mineral zilbermintsite-(La), ideally (CaLa5)(Fe3+Al3Fe2+)[Si2O7][SiO4]5O(OH)3, was found in a single polymineralic nodule from the Mochalin Log REE deposit, Chelyabinsk Oblast, South Urals, Russia. Zilbermintsite-(La) forms anhedral grains up to 0.65 × 0.20 mm at the contact of ferriperbøeite-(La), törnebohmite-(La) and ferriallanite-(Ce). Other associated minerals include bastnäsite-(La), biraite-(La), ferriallanite-(La), ferriperbøeite-(Ce), fluorbritholite-(Ce), monazite-(La), perbøeite-(La), percleveite-(Ce), percleveite-(La), perrierite-(Ce), perrierite-(La), thorianite, thorite and quartz. The new mineral is light brown, translucent in thin fragments with a vitreous lustre. It is brittle, with good {100} cleavage. Mohs hardness is ca. 6. Dcalc = 4.684 g cm–3. Optically, zilbermintsite-(La) is biaxial (+), α = 1.805(7), β = 1.812(7) and γ = 1.867(8) (589 nm); 2Vmeas = 40(15)° and 2Vcalc = 40°. The empirical formula based on O28(OH,F)3 apfu is (Ca0.94La2.56Ce2.18Nd0.20Pr0.10Th0.02)Σ6.00(Al2.96Fe3+0.90Fe2+0.64Mg0.34Mn0.13Ti0.03)Σ5.00Si7.00O28[(OH)2.42F0.58]. Zilbermintsite-(La) is monoclinic, P21/m; the unit-cell parameters are: a = 8.9605(5), b = 5.7295(2), c = 25.1033(13) Å, β = 116.616(7), V = 1152.21(12) Å3 and Z = 2. The crystal structure of zilbermintsite-(La) is solved from the single-crystal X-ray diffraction data [R = 0.0757 for 2857 unique reflections with I > 2σ(I)]. The new mineral is isotypic to radekškodaite-(La) and radekškodaite-(Ce) and together with them forms the newly defined radekškodaite group. All members of this group possess the ET2 type structure where one epidote-type module (E) regularly alternates with two törnebohmite-type modules (T). The new mineral honours Professor Veniamin A. Zilbermints (1887–1939) who was a pioneer of the study of the Mochalin Log deposit. The Levinson suffix-modifier -(La) indicates the predominance of La among rare-earth elements in the mineral.

Škáchaite (IMA2022–143) is a new mineral species discovered in samples from the hydrothermal vein B117, shaft No. 6 at the Brod deposit of the uranium and base-metal Příbram ore district, central Bohemia, Czech Republic. Škáchaite is a Co-dominant member of the dolomite group and forms anhedral grains up to 50 μm in size and as 20–100 μm thick growth zones in škáchaite–dolomite crystals as a part of carbonate (dolomite, calcite, siderite, spherocobaltite, ankerite, kutnohorite and minrecordite) gangue, associated with native silver, sulfides and arsenides. Škáchaite is pale to bright pink with vitreous lustre. The Mohs hardness is ca. 3½–4, similar to other members of the dolomite group. The calculated density is 3.140 g.cm–3. Škáchaite is optically uniaxial (–); the indices of refraction are ω = 1.741(3) and ɛ = 1.535(3). On the basis of electron-microprobe analyses, its empirical formula is Ca1.00(Co0.45Mg0.38Ca0.08Fe0.05Mn0.03Zn0.01)Σ1.00(CO3)2. The ideal formula is CaCo(CO3)2, which requires (in wt.%) CaO 25.60, CoO 34.21, CO2 40.19, a total of 100.00. Škáchaite is trigonal, R$\bar{3}$, with unit-cell parameters a = 4.8177(18), c = 16.093(7) Å, V = 323.5(2) Å3 and Z = 3. The strongest reflections of the calculated powder X-ray diffraction pattern [d, Å, (Irel, %) hkl] are: 3.704 (13) 10$\bar{2}$; 2.896 (100) 104; 2.409 (15) 110; 2.019 (17) 202; 1.812 (19) 10$\bar{8}$; and 1.792 (16) 11$\bar{6}$. According to the single-crystal X-ray diffraction data (R1 = 0.0304 for 94 reflections with [I > 3σ(I)]), the crystal structure of škáchaite is isotypic with its Mg-analogue, dolomite. The Raman spectrum of škáchaite, as well as the tentative assignment of observed bands, are given in this paper. The mineral is named in honour of Pavel Škácha, a Czech mineralogist and curator of the mineralogical collection of the Mining Museum Příbram, Czech Republic.

Kristjánite, KNa2H(SO4)2, is a new mineral (IMA2022–131) found in a high-temperature fumarole on Fimmvörðuháls, Iceland. It is monoclinic, P21/n, a = 6.9625(1), b = 9.9953(1), c = 11.0928(2) (Å), β = 105.637(2)° and V = 743.40(2) Å3. Kristjánite forms colourless transparent crystals up to ~100 μm in size in compact aggregates with metathénardite, belomarinaite, aphthitalite, ivsite and an unknown mineral with tentative composition K2NaH(SO4)2, or grows in white globules of smaller grains on their surface. The eight strongest maxima in a powder X-ray diffraction diagram are [d, Å (Intensity)] 4.37 (59), 3.65 (32), 3.48 (78), 3.36 (100), 3.18 (76), 2.83 (43), 2.73 (38) and 2.405 (23). The mineral represents a novel crystal structure type. In it, K is coordinated by eight O atoms, and two symmetrically independent Na atoms by seven O atoms. Two symmetrically independent S atoms are in tetrahedral coordination by O atoms. A close to linear, very short hydrogen bond (2.44 Å), connects the two to a SO4–H–SO4 dimer. K and Na coordination polyhedra share vertices, edges and even faces forming with sulfate tetrahedra a tight structure with narrow [100] channels lined on two opposite sides by hydrogen bonds.

Enricofrancoite (IMA2023–002), ideally KNaCaSi4O10, is a new litidionite-group member found as the product of high-temperature alteration of hosting silicates with the enrichment by Cu-bearing fluids at the rock–fumaroles interface related to the 1872 eruption of Somma–Vesuvius volcano, southern Italy. It occurs as euhedral and platy crystals or crusts together with litidionite, tridymite, wollastonite and Al- and Fe-bearing diopside, kamenevite, perovskite, rutile, Ti-rich magnetite and colourless Si-glass. Single crystals of enricofrancoite are transparent colourless or light blue with a vitreous lustre. Mohs hardness is 5.5. Dmeas is 2.63(3) g/cm3 and Dcalc is 2.63 g/cm3. The mineral is optically biaxial (−), α = 1.542(5), β = 1.567(5),γ = 1.575(5); 2V(meas) = 60(2)° and 2Vcalc = 58°. The mean chemical composition (wt.%, electron-microprobe data) is: SiO2 64.81, Al2O3 0.03, TiO2 0.08, FeO 0.07, MgO 1.71, CaO 10.64, CuO 2.22, Na2O 8.56, K2O 11.41, total 99.94. The empirical formula based on 10 O apfu is: K0.90Na1.03(Ca0.71Mg0.16Cu0.10)Σ0.97Si4.02O10. The Raman spectrum contains bands at 133, 248, 265, 290, 335, 400, 438, 510, 600, 690 and 1120 cm–1 and the wavenumbers of the IR absorption bands are: 424, 470, 492, 530, 600, 630, 690, 750, 788, 970, 1040 and 1160 cm–1. The eight strongest lines of the powder X-ray diffraction pattern are [d, Å (I, %) hkl]: 6.75 (42) 01$\bar{1}$, 3.65 (20) 11$\bar{2}$, 3.370 (100) 02$\bar{2}$, 3.210 (52) 102, 3.051 (18) 111, 3.033 (25) 2$\bar{1}\bar{2}$, 2.834 (22) 02$\bar{3}$ and 2.411 (72) 03$\bar{2}$. Enricofrancoite is triclinic, space group P$\bar{1}$, unit-cell parameters refined from the single-crystal data are a = 7.0155(4) Å, b = 8.0721(4) Å, c = 10.0275(4) Å, α = 104.420(4)°, β = 99.764(4)°, γ = 115.126(5)° and V = 472.74(5) Å3. The crystal structure has been refined from single-crystal X-ray diffraction data to R1 = 0.035 on the basis of 2078 independent reflections with Fo > 4σ(Fo). Enricofrancoite is an H2O-free analogue of calcinaksite with 5-coordinated Ca2+ at the M site.

The new columbite-supergroup mineral dmitryvarlamovite, ideally Ti2(Fe3+Nb)O8, was discovered in weathered alkaline metasomatic assemblages formed after late Riphaean sedimentary carbonate rocks of the Verkhne-Shchugorskoe deposit, Middle Timan Mts., Russia. The associated minerals are columbite-(Fe), pyrochlore-group minerals, monazite-(Ce), xenotime-(Y), baryte, pyrite, drugmanite and plumbogummite. Dmitryvarlamovite occurs as isolated anhedral equant grains up to 0.5 mm across. The colour of dmitryvarlamovite is black, the streak is black and the lustre is submetallic. The new mineral is brittle, with the mean VHN hardness of 753 kg mm–2 corresponding to the Mohs’ hardness of 6. No cleavage is observed. The fracture is conchoidal. The calculated density is 4.891 g⋅cm–3. In reflected light, dmitryvarlamovite is light grey; no pleochroism is observed. The reflectance values (Rmin, % / Rmax, % / λ, nm) are: 19.8/20.3/470, 18.3/18.9/546, 17.8/18.5/589 and 17.3/17.8/650. The chemical composition is (electron microprobe data, with iron divided into Fe2O3 and FeO based on the charge balance, wt.%): MnO 0.11, FeO 1.51, V2O3 0.89, Cr2O3 0.28, Fe2O3 19.26, TiO2 37.72, Nb2O5 40.08, total 99.85. The IR and Raman spectra indicate the absence of H-, C- and N-bearing groups. The empirical formula is (Fe2+0.08V3+0.05Cr3+0.01Fe3+0.92Ti1.79Nb1.15)Σ4.00O8. The crystal structure was determined using single-crystal X-ray diffraction data and refined to R = 0.048. Dmitryvarlamovite is orthorhombic, space group P21212, a = 4.9825(6), b = 4.6268(4), c = 5.5952(6) Å and V = 5.5952(6) Å3 (Z = 1). The structure is related to those of wolframite-group minerals but differs in the scheme of cation ordering. The crystal-chemical formula derived based on the structural data is (Ti0.57Nb0.21Fe3+0.15Fe2+0.04V0.02Cr0.01)2(Nb0.36Ti0.33Fe3+0.31)2O8. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 3.58 (40) (011), 2.911 (100) (111), 2.809 (40) (002), 2.497 (38) (020), 2.447 (29) (103), 1.7363 (32) (103) and 1.7047 (29) (220). Dmitryvarlamovite is named after Dmitry Anatol'evich Varlamov (b. 1965).