Stibiogoldfieldite, Cu12(Sb2Te2)S13, was approved as a new mineral species from the Mohawk mine, Goldfield mining district, Esmeralda County, Nevada, USA. It occurs as metallic anhedral grains, dark grey in colour. It is associated with quartz, pyrite and an Ag–Bi–(S,Se) phase (holotype material) and with quartz, pyrite, calaverite, bismuthinite, bohdanowiczite, and the Ag–Bi–(S,Se) phase (cotype material). In reflected light, stibiogoldfieldite is isotropic, grey in colour, with indistinct brownish shade. Reflectance data in air [R (%)] are: 31.1 at 470 nm, 30.9 at 546 nm, 30.8 at 589 nm and 31.0 at 650 nm. Electron microprobe analysis for holotype material gave (in wt.% – average of 60 spot analyses): Cu 45.03(60), Ag 0.26(7), Fe 0.02(3), Zn 0.13(15), Sn 0.02(4), Pb 0.05(6), Sb 8.02(62), As 2.80(65), Bi 2.77(87), Te 15.15(1.24), S 24.50(32), Se 0.52(11), total 99.27(69). On the basis of (As + Sb + Te + Bi) = 4 atoms per formula unit (apfu), the empirical formula of stibiogoldfieldite is (Cu12.05Ag0.04Zn0.03Fe0.01)Σ12.13(Sb1.12As0.63Bi0.23Te2.02)Σ4.00(S12.99Se0.11)Σ13.10. Chemical data on an additional sample from the same locality (cotype material) gave the following results (in wt.% – average of 181 spot analyses): Cu 43.84(63), Ag 0.21(7), Sb 5.92(78), As 2.63(45), Te 20.07(1.19), S 25.13(53), Se 0.97(35), total 99.47(66). On the basis of (As + Sb + Te + Bi) = 4 apfu, the empirical formula of cotype material is (Cu11.30Ag0.03)Σ11.33(Sb0.80As0.57Bi0.06Te2.57)Σ4.00(S12.83Se0.20)Σ13.03. Stibiogoldfieldite is cubic, I$\overline 4$3m, with unit-cell parameters a = 10.3466(17) Å, V = 1107.6(5) Å3 and Z = 2 (holotype). Unit-cell parameters for the cotype sample are a = 10.3035(2) Å and V = 1093.83(7) Å3. The crystal structure of holotype stibiogoldfieldite was refined by single-crystal X-ray diffraction data to a final R1 = 0.032 on the basis of 285 reflections with Fo > 4σ(Fo) and 20 refined parameters. Stibiogoldfieldite is isotypic with other members of the tetrahedrite group.

Sluzhenikinite, Pd15(Sb7–xSnx) with 3 ≤ x ≤ 4, is a new mineral discovered in the pegmatoidal galena–chalcopyrite massive ore from the Oktyabrsk mine, Oktyabrsk deposit of the Noril`sk deposits, Russia. Sluzhenikinite forms euhedral elongate lamellar crystals (100–150 μm long and 10–50 μm wide) associated with Au–Ag alloy, insizwaite and myrmekitic intergrowths of Pt–Pd minerals (stibiopalladinite, maslovite and sobolevskite), in close association of sperrylite and base-metal sulfides (galena, chalcopyrite, cubanite and pentlandite). In plane-polarised light, sluzhenikinite is pale brown with weak bireflectance, imperceptible pleochroism, and weak anisotropy with straw yellow to deep blue rotation tints; it exhibits no internal reflections. Reflectance values for sluzhenikinite in air (R1,R2 in %) are: 46.2, 46.5 at 470nm; 52.1, 52.2 at 546nm; 54.7, 55.1 at 589nm; and 57.8, 59.0 at 650nm. Thirteen electron-microprobe analyses of sluzhenikinite gave an average composition: Pd 65.06, Sn 15.60 and Sb 19.58, total 100.24 wt.%, corresponding to the formula Pd14.88(Sb3.92Sn3.20)Σ7.12 based on 22 atoms; the average of twenty-one energy dispersive spectroscopy analyses on co-type material gave: Pd 63.36, Pt 1.15, Sn 16.28 and Sb 19.21, total 100.00 wt.%, corresponding to the formula (Pd14.62Pt0.14)Σ14.76(Sb3.87Sn3.37)Σ7.24. The density, calculated on the basis of the empirical formula, is 11.22 g/cm3. The mineral is monoclinic, space group P21/m, with a = 7.5558(1), b = 29.2967(3), c = 7.5713(1) Å, β = 119.931(2)°, V = 1452.44(4) Å3 and Z = 4. The crystal structure was determined using data from single-crystal X-ray diffraction and demonstrates conclusively that the correct stoichiometry is Pd15(Sb,Sn)7, rather than Pd2(Sb,Sn); R1 = 0.035, wR2 = 0.073, GoF = 1.118 for 209 refined parameters and 4738 unique reflections. The mineral is named after Sergey Fedorovich Sluzhenikin, an expert on platinum-group minerals, particularly from the area of the type locality.

The response of garnet and zircon to prograde amphibolite-facies metamorphism in late Proterozoic mica schists from the Scottish Highlands has been investigated. Spatial analysis of zircon populations using scanning electron microscopy was undertaken in Dalradian Schists that have undergone a sequence of prograde garnet growth and localised breakdown reactions involving coupled dissolution–reprecipitation. Fluid availability and matrix permeability strongly control this metamorphic response and different generations of garnet contain radically different populations of metamorphic micro-zircon and associated changes in the detrital zircon population. Micro-zircon abundance increases during garnet growth, whereas that of detrital zircon decreases. The mineralogy of the matrix influences zircon abundance in porphyroblast phases, where garnet overgrows a micaceous matrix zircon-rich garnet forms and where it overgrows a quartzofeldspathic matrix the result is zircon-poor garnet. Following garnet growth, micro-zircon abundance decreases at each stage of the prograde reaction history, with sillimanite-zone schists containing the lowest abundance, suggesting micro-zircons are texturally less stable at staurolite- and sillimanite-grade metamorphism. Micro-zircons are distributed evenly across host minerals in the matrix, with the exception of retrograde chlorite where micro-zircons are absent due to fluids removing Zr before new zircon can precipitate. There is an overall decrease in the mode of zircon at each stage of the reaction history, indicating that zircon is a highly reactive phase during amphibolite-facies metamorphism and is very sensitive to individual prograde and retrograde reactions.

Dendoraite-(NH4), (NH4)2NaAl(C2O4)(PO3OH)2(H2O)2, is a new mineral species from the Rowley mine, Maricopa County, Arizona, USA. It occurs in an unusual bat-guano-related, post-mining assemblage of phases that include a variety of vanadates, phosphates, oxalates and chlorides, some containing NH4+. Other secondary minerals found in association with dendoraite-(NH4) are antipinite, fluorite, mimetite, mottramite, relianceite-(K), rowleyite, salammoniac, struvite, vanadinite, willemite, wulfenite and at least one other new mineral. Crystals of dendoraite-(NH4) are colourless blades up to ~0.1 mm in length. The streak is white and lustre is vitreous, Mohs hardness is 2½, tenacity is brittle and fracture is splintery. The calculated density is 2.122 g⋅cm–3. Dendoraite-(NH4) is optically biaxial (–) with α = 1.490(5), β = 1.540(5) and γ = 1.541(5) (white light); 2Vcalc = 15.7°; and orientation X = b. Electron microprobe analysis gave the empirical formula [(NH4)1.48K0.52]Σ2.00Na0.96(Al0.96Fe3+0.03)Σ0.99(C2O4)[PO2.97(OH)1.03]2(H2O)2, with the C, N and H contents constrained by the crystal structure. Dendoraite-(NH4) is monoclinic, P21/n, with a = 10.695(6), b = 6.285(4), c = 19.227(12) Å, β = 90.933(10)°, V = 1292(2) Å3, and Z = 4. The structural unit in the crystal structure of dendoraite-(NH4) (R1 = 0.0467 for 1322 Io > 2σI reflections) is a double-strand chain of corner-sharing AlO6 octahedra and PO3OH tetrahedra decorated by additional PO3OH tetrahedra and C2O4 groups. Topologically, this is the same chain found in the structure of thebaite-(NH4). The decorated chains connect to one another through links to NaO7(H2O) polyhedra to form a [Na(H2O)Al(C2O4)(PO3OH)2]2– sheet, which connect to one another through bonds to (NH4)/K and through hydrogen bonds.

Magnesiobermanite, MgMn3+2(PO4)2(OH)2⋅4H2O, is a new secondary phosphate mineral and the Mg analogue of bermanite found in a granitic pegmatite at the White Rock No.2 quarry situated in the Bimbowrie Conservation Park, South Australia, Australia. Magnesiobermanite occurs as aggregates of twinned, bladed to tabular crystals, up to 1.2 mm across. Individual crystals are up to 0.3 mm in length. The crystals are orange–red to brownish red, with a vitreous lustre and a salmon-pink streak. The mineral is brittle with a conchoidal fracture and a good cleavage on {100}. The mineral is biaxial (–), with α = 1.690(2), β = 1.719(2) and γ = 1.734(2) (white light). The calculated 2V is 70.4°. Electron microprobe analyses provided: MgO 9.59, Mn2O3 27.41, Fe2O3 8.84, Al2O3 0.18, P2O5 33.27, H2O 20.94, total 100.23 wt.%. The empirical formula (based on 14 O atoms) is: Mg1.02(Mn3+1.49Fe3+0.47Al0.02)1.98(PO4)2.01(OH)1.95⋅4.01H2O. Magnesiobermanite is monoclinic, space group P21, with the unit-cell parameters: a = 5.4215(11), b = 19.072(4), c = 5.3889(11) Å, β = 110.21(3)°, V = 522.89(18) Å3 and Z = 2. The crystal structure was refined to an R1 index of 2.43% based on for 3222 observed reflections with Fo > 4σ(Fo). Magnesiobermanite is isostructural with bermanite, Mn2+Mn3+2(PO4)2(OH)2⋅4H2O, from which it derives its name. The structure is based upon a sheet of the form [(M(OH)2(PO4)2] in the (010) plane. Sheets are linked in the b direction by [M3(H2O)4O2] octahedra and by hydrogen bonds.

Relianceite-(K), K4Mg(V4+O)2(C2O4)(PO3OH)4(H2O)10, is a new mineral species from the Rowley mine, Maricopa County, Arizona, USA. It occurs in an unusual bat-guano-related, post-mining assemblage of phases. Other secondary minerals associated with relianceite-(K) are antipinite, dendoraite-(NH4), fluorite, mimetite, mottramite, rowleyite, salammoniac, struvite, vanadinite, willemite, wulfenite and at least one other new mineral. Crystals of relianceite-(K) are sky blue prisms up to ~0.1 mm in length. The streak is very pale blue and lustre is vitreous, Mohs hardness is 2½, tenacity is brittle and fracture is splintery. The calculated density is 2.111 g⋅cm–3. Relianceite-(K) is optically biaxial (+) with α = 1.528(2), β = 1.529(2), γ = 1.562(2) (white light); 2Vmeas = 22(1)°; orientation Z = b; pleochroism: X = colourless, Y = pale blue, Z = pale blue; X < Y ≈ Z. Electron microprobe analysis gave the empirical formula [K2.21(NH4)1.79]Σ4.00Mg0.96(V4+0.95O)2(C2O4)[P1.03O3.03(OH)0.97]4(H2O)10, with the C, N and H contents constrained by the crystal structure. Raman spectroscopy confirmed the presence of NH4 and C2O4. Relianceite-(K) is monoclinic, Pc, with a = 12.404 (7) Å, b = 9.014 (6), c = 13.260 (8) Å, β = 100.803(10)°, V = 1456 (2) Å3 and Z = 2. The structural unit in the crystal structure of relianceite-(K) (R1 = 0.0540 for 3751 Io > 2σI reflections) is a (V4+O)2(C2O4)(PO3OH)4 chain in which VO6 octahedra are bridged by an oxalate group to form [V2C2O12] dimers, PO3OH tetrahedra form a double bridge between the VO6 octahedra of the dimers, and additional PO3OH tetrahedra decorate the chain. Topologically, this is the same chain found in the structure of davidbrownite-(NH4). The MgO(H2O)5 octahedron can be considered a distant decoration on the chain. The chains are linked to each other through an extensive system of K/NH4–O bonds and hydrogen bonds.

The new mineral paramarkeyite (IMA2021-024), Ca2(UO2)(CO3)3⋅5H2O, was found in the Markey mine, San Juan County, Utah, USA, where it occurs as a secondary phase on gypsum-coated asphaltum in association with andersonite, calcite, gypsum and natromarkeyite. Paramarkeyite crystals are transparent, pale green-yellow, striated tablets, up to 0.11 mm across. The mineral has white streak and vitreous lustre. It exhibits moderate bluish-white fluorescence (405 nm laser). It is very brittle with irregular, curved fracture and a Mohs hardness of 2½. It has an excellent {100} cleavage and probably two good cleavages on {010} and {001}. The measured density is 2.91(2) g cm–3. Optically, the mineral is biaxial (–) with α = 1.550(2), β = 1.556(2), γ = 1.558(2) (white light); 2V = 60(2)°; strong r > v dispersion; orientation: Y = b; nonpleochroic. The Raman spectrum exhibits bands consistent with UO22+, CO32– and O–H. Electron microprobe analysis provided the empirical formula (Ca1.83Na0.20Sr0.03)Σ2.05(UO2)(CO3)3⋅5H2O (+0.07 H). Paramarkeyite is monoclinic, P21/n, a = 17.9507(7), b = 18.1030(8), c = 18.3688(13) Å, β = 108.029(8)°, V = 5676.1(6) Å3 and Z = 16. The structure of paramarkeyite (R1 = 0.0647 for 6657 I > 2σI) contains uranyl tricarbonate clusters that are linked by Ca–O polyhedra to form heteropolyhedral layers. The structure of paramarkeyite is very similar to those of markeyite, natromarkeyite and pseudomarkeyite.

Armellinoite-(Ce), ideally Ca4Ce4+(AsO4)4⋅H2O, is a new mineral discovered in Fe–Mn ore in metaquartzites of the Montaldo mine, Corsaglia Valley, Cuneo Province, Piedmont, Italy. It occurs as very small and rare, pale yellow to brown–yellow pseudo-octahedral translucent crystals hosted by a matrix of quartz, hematite, cryptomelane/hollandite, tilasite, muscovite, braunite and montmorillonite. The mineral is translucent, with white streak and has a resinous to vitreous lustre. It is brittle with irregular fracture and fair cleavage parallel to {110} and {100}. Estimated Mohs hardness is ~3–3.5. Calculated density is 4.29 g⋅cm–3. Armellinote-(Ce) is uniaxial (–), ω = 1.795(5), ɛ = 1.765(5) (white light), non-pleochroic and non-fluorescent. Chemical point analyses by WDS-EPMA yielded the empirical formula (based on 17 O+F anions): A(Ca3.89Th0.08Sr0.02La0.03)Σ4.02B(Ce4+0.76Nd0.13Y0.08Gd0.03Sm0.02Pr0.01Dy0.01Ho0.01)Σ1.05[(As4.00P0.01)Σ4.01O4]4⋅(H2O0.85F0.15)Σ2.00. The presence of H2O was confirmed by Raman spectroscopy. The mineral is tetragonal, I41/a, with single-crystal unit-cell parameters a = 10.749(2), c = 12.030(2) Å and V = 1390.0(6) Å3, with Z = 4. The eight strongest X-ray powder diffraction lines are [d Å (Irel; hkl)]: 7.983 (36; 101), 4.443 (23; 2̄11), 2.957 (100; 3̄12), 2.398 (14; 420), 1.875 (22; 424, 325), 1.728 (19; 3̄16), 1.612 (13; 613) and 1.475 (26; 712, 552). The crystal structure (R1 = 0.0284 for 1275 unique reflections) has isolated TO4 (T = As5+) tetrahedra that link Ca2+- or Ce4+-centred polyhedra via common oxygen ligands to form 2D blocks or double-layered (DL) structural units parallel to (001). Armellinoite-(Ce) is isostructural with pottsite, ideally (Pb3Bi)Bi(VO4)4⋅H2O, and closely related to a larger number of anhydrous synthetic compounds. The mineral is named after the mineral collector Gianluca Armellino (b. 1962), who collected the discovery sample.

The new sodalite-group mineral sapozhnikovite, ideally Na8(Al6Si6O24)(HS)2, was discovered in a hydrothermally altered urtite-like rock at Karnasurt Mountain, Lovozero alkaline massif, Kola Peninsula, Russia. The associated minerals are nepheline, aegirine, potassic feldspar, albite, kyanoxalite, natrolite, fluorapatite, fluorcaphite, lomonosovite (partially or completely altered to murmanite) and loparite-(Ce). Sapozhnikovite forms isolated colourless to pale greyish anhedral equant grains up to 5 mm across. The streak is white and the lustre is vitreous. Strong orange fluorescence under longwave UV radiation (λ = 330 nm) and weak yellow-orange fluorescence under shortwave UV radiation (λ = 245 nm) is observed. Sapozhnikovite is brittle, with a Mohs hardness of 5½. Cleavage is imperfect on (110). Density measured by flotation in heavy liquids is equal to 2.25(1) g⋅cm–3. The calculated density is 2.255 g⋅cm–3. Sapozhnikovite is characterised by infrared, Raman, electron spin resonance, NIR-Vis-UV absorption, and photoluminescence spectroscopy. The chemical composition is (wt.%, electron microprobe, H2O determined by gas chromatography of ignition products): Na2O 25.05, Al2O3 32.44, SiO2 37.58, HS 4.33, Cl 2.22, H2O 0.30, –O≡(Cl,HS) –1.55, total 100.37. The empirical formula is Na7.73Al6.08Si5.97O24(HS)1.25Cl0.60⋅0.16H2O. The crystal structure was determined using single-crystal X-ray diffraction data and refined to R1 = 1.62%. Sapozhnikovite is cubic, P$\bar{4}$3n, with a = 8.9146(1) Å, V = 708.45(2) Å3 and Z = 1. The new mineral is isostructural with sodalite. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 6.30 (37) (110), 3.638 (100) (211), 2.821 (14) (310), 2.572 (18) (222), 2.382 (16) (321) and 2.101 (29) (411). The mineral is named in honour of the Russian mineralogist and crystallographer Dr. Anatoly Nikolaevich Sapozhnikov (b. 1946).

Hydroplumboelsmoreite (IMA21-C), (Pb,□)2(W,Fe3+)2O6(H2O), is a redefined elsmoreite-group mineral in the pyrochlore supergroup. It was found in a ‘jixianite’ cotype specimen provided by Mr. Liu Jianchang, who first found ‘jixianite’ in 1979 in the Jizhou District, Tianjin City, China. The mineral occurs as yellow to reddish brown aggregates, together with raspite and another elsmoreite-group mineral under study. Hydroplumboelsmoreite occurs in cryptocrystalline form and occasionally in octahedral microcrystalline form (under 20 μm in size). The crystals are colourless and translucent with a white streak, and the lustre is adamantine to greasy. Hydroplumboelsmoreite is isotropic, with a calculated refractive index of 2.29, a Mohs hardness of ~4½–5, and a calculated density of 7.47 g⋅cm−3. The strongest five powder X-ray diffraction lines [d in Å(I)(hkl)] are 6.070(28)(111), 3.012(100)(222), 2.603(32)(004), 1.836(35)(044) and 1.568(30)(226). The crystal structure was refined to R1 = 0.0459 using 80 unique reflections collected with MoKα radiation, and the results show that the mineral is cubic, space group Fd$\bar{3}$m, with a = 10.3377(5) Å, V = 1104.77(16) Å3 and Z = 8. Electron microprobe analyses and crystal structure refinement were used to determine the empirical formula: (Pb1.05Sr0.05Ce3+0.07Na0.01□0.82)Σ2.00(W1.32Fe3+0.67Zr0.01)Σ2.00O6[(H2O)0.43O0.19□0.38]Σ1.00. The mineral was named hydroplumboelsmoreite based on the predominance of Pb, W, and molecular H2O in the A, B and Y sites, respectively.

A new occurrence of kintoreite, ideally PbFe3(PO4)(PO3OH)(OH)6, is described from the Tripi mine, Alì, Peloritani Mountains, northeastern Sicily, Italy. Kintoreite occurs as yellow equant crystals, up to 0.05 mm in size, on quartz, associated with another alunite-supergroup mineral currently under study. The studied grains of kintoreite are chemically zoned, showing the occurrence of two distinct domains. Electron microprobe analyses gave (in wt.%): SO3 5.47(27), P2O5 17.55(14), Al2O3 7.81(35), Fe2O3 23.81(44), PbO 35.11(41), H2Ocalc 9.93, total 99.68 (darker domains) and SO3 6.03(5), P2O5 16.66(23), Al2O3 4.22(2), Fe2O3 27.31(6), PbO 33.78(22), H2Ocalc 10.25, total 98.25 (brighter domains). On the basis of 14 O atoms per formula unit (apfu) and (P+S) = 2 apfu, the darker and brighter domains have chemical formula Pb1.00(Fe3+1.89Al0.97)Σ2.86[P1.57S0.43O7.43(OH)0.57][(OH)5.58(H2O)0.42]Σ6.00 and Pb0.98(Fe3+2.21Al0.53)Σ2.74[P1.51S0.49O7.49(OH)0.51][(OH)5.18(H2O)0.82]Σ6.00, respectively. Single-crystal X-ray diffraction was performed on a grain extracted from the same sample. Unit-cell parameters are a = 7.2191(10), c = 16.834(3) Å, V = 759.8(3) Å3 and Z = 3; space group R$\bar{3}$m. The crystal structure was refined on the basis of 226 unique reflections with Fo > 4σ(Fo) and 31 least-square parameters to R1 = 0.0415. Kintoreite is isotypic with other alunite-supergroup minerals. Micro-Raman spectroscopy suggests the possible occurrence of H2O groups, supporting the possible protonation of (OH) groups as a charge-balance mechanism in this mineral. Kintoreite may play an environmental role in the Alì area, where previous authors detected high concentrations of potentially toxic elements in soils.

Gallium (Ga) and germanium (Ge) are technologically important critical elements. Lead blast furnace slags from Tsumeb, Namibia, comprise over two million metric tons of material that contains high levels of Ga (135–156 ppm) and Ge (128–441 ppm) in addition to significant Zn concentrations (up to 11 wt.%) and represent a potential resource for these elements. A combination of mineralogical and chemical methods (PXRD, FEG-SEM-EPMA and LA-ICP-MS) indicated different partitioning of Ga and Ge within the individual slag phases. Gallium is predominantly bound in small euhedral crystals of Zn–Fe–Al spinels (<10 μm in size), exhibiting concentrations in the range of 480–1370 ppm (up to 0.004 atoms per formula unit, apfu). Concentrations of Ga in other phases (e.g. melilite) are systematically below 90 ppm. The principal host of Ge is the silicate glass and, to a lesser extent, silicates (melilite and olivine group phases). Concentrations of Ge in glass attained a concentration of 470 ppm (EPMA), but the LA-ICP-MS analysis of glass matrix containing submicrometre spinel crystallites indicated that average Ge levels vary in the range of 113–394 ppm. In the potential extraction of Ga and Ge, the results indicate that ultrafine milling is needed to liberate the Ga- and Ge-hosting phases prior to metallurgical processing of the slag.