Okruginite, Cu2SnSe3 is a new mineral discovered from the high-sulfidation epithermal Au Ozernovskoye deposit, Kamchatka peninsula, Russia. It occurs as distinct Se-rich zones in Se-bearing mohite crystals or forms aggregates of small crystals 10–15 μm in size in quartz. In plane-polarised light, okruginite appears brownish grey. Pleochroism and bireflectance are discernible, anisotropy is weak, with rotation tints pale blue-grey to pale grey-brown; it exhibits no internal reflections. Reflectance values of the synthetic analogue of okruginite in air (R1, R2 in %) are: 25.9, 26.5 at 470 nm, 27.5, 26.5 at 546 nm, 27.8, 28.4 at 589 nm and 27.7, 28.4 at 650 nm. Twenty seven electron-microprobe analyses of okruginite give an average composition: Cu 29.48, Sn 28.10, Se 33.40 and S 8.75, total 99.73 wt.%, corresponding to the empirical formula Cu1.99Sn1.02(Se1.82S1.17)Σ2.99 based on 6 atoms; the average of seven analyses on its synthetic analogue is: Cu 23.62, Sn 24.37 and Se 49.09, total 97.08 wt.%, corresponding to Cu1.86Sn1.03Se3.11. The density, calculated on the basis of the empirical formula, is 5.126 g/cm3. The mineral is monoclinic, space group Cc, with a = 6.9906(2), b = 12.0712(4) Å, c = 6.9723(2) Å, β = 109.350(10)°, V = 555.1(2) Å3 and Z = 4. The crystal structure was solved and refined from the powder X-ray-diffraction data of synthetic Cu2SnSe3. Okruginite is the selenium-end member of the Cu2SnS3–Cu2SnSe3 solid solution. The mineral name is in honour of Dr. Victor Mikhailovich Okrugin, a Russian mineralogist, for his contributions to mineralogy and geology of epithermal deposits, in particular of the Au–Ag deposits in Kamchatka.

Svetlanaite, SnSe is a new mineral discovered from the high-sulfidation epithermal Au-deposit Ozernovskoe, Kamchatka peninsula, Russia. It forms tiny euhedral spindles (0.5–2 μm × 10–15 μm) in quartz, in close association with cassiterite, rutile, mohite, mawsonite, kiddcreekite, hemusite, tellurium, kostovite and Se-bearing ‘fahlores’ (Se-goldfieldite–Se(Bi)-tetrahedrite–Se-tennantite). In plane-polarised light, svetlanaite is light-grey, pleochroic from white to cream and strongly anisotropic in shades of light blue, dark blue, khaki and orange–brown; it exhibits no internal reflections. Reflectance values of synthetic analogue of svetlanaite in air (R1,R2 in %) are: 50.9, 56.5 at 470 nm, 50.2, 56.7 at 546 nm, 49.5, 55.3 at 589 nm and 48.7, 53.4 at 650 nm. Twelve electron-microprobe analyses of svetlanaite give an average composition: Sn 61.30, Se 37.22 and S 1.25 total 99.79 wt.%, corresponding to the empirical formula Sn1.01(Se0.92S0.07)Σ0.99 based on 2 atoms; the average of seven analyses on its synthetic analogue is: Sn 59.98 and Se 39.71, total 99.59 wt.%, corresponding to Sn1.00Se1.00. The density, calculated on the basis of the empirical formula, is 6.08 g/cm3. The mineral is orthorhombic, space group Pnma, with a = 11.500(2), b = 4.154(2), c = 4.445(2) Å, V = 212.34(14) Å3 and Z = 4. The crystal structure was solved and refined from the powder X-ray-diffraction data of synthetic SnSe. It crystallises in the GeS-structure type. It is isostructural with the mineral herzenbergite (SnS). The mineral name is in honour of Svetlana K. Smirnova, a Russian mineralogist, for her contributions to geology in the epithermal Au–Ag deposits of the Tien–Shan region.

Nipalarsite, Ni8Pd3As4, is a new platinum-group mineral discovered in the sulfide-bearing orthopyroxenite of the Monchetundra layered intrusion, Kola Peninsula, Russia (67°52′22″N, 32°47′60″E). Nipalarsite forms anhedral grains (5–80 µm in size) in intergrowths with sperrylite, kotulskite, hollingworthite, isomertieite, menshikovite, palarstanide, nielsenite and monchetundtraite enclosed in pentlandite, anthophyllite, actinolite and chlorite. Nipalarsite is brittle, has a metallic lustre and a grey streak. In plane-polarised light, nipalarsite is light grey with a blue tinge. Reflectance values in air (in %) are: 46.06 at 470 nm, 48.74 at 546 nm, 50.64 at 589 nm and 54.12 at 650 nm. Values of VHN20 fall between 400.5 and 449.2 kg.mm–2, with a mean value of 429.9 kg.mm–2, corresponding to a Mohs hardness of ~4. The average result of 27 electron microprobe wavelength dispersive spectroscopy analyses of nipalarsite is (wt.%): Ni 44.011, Pd 28.74, Fe0.32, Cu 0.85, Pt 0.01, Au 0.05, As 25.42, Sb 0.05, Te 0.39, total 99.85. The empirical formula (normalised to 15 atoms per formula unit) is: (Ni8.10Fe0.06)Σ8.16(Pd2.94Cu0.18)Σ3.12(As3.68Te0.03)Σ3.71 or, ideally, Ni8Pd3As4. Nipalarsite is cubic, space group Fm$\bar{3}$m, with a = 11.4428(9) Å, V = 1498.3(4) Å3 and Z = 8. The strongest lines in the powder X-ray diffraction pattern of synthetic Ni8Pd3As4 [d, Å (I) (hkl)] are: 2.859(10)(004), 2.623(6)(313), 2.557(6)(024), 2.334(11)(224), 2.201(35)(115,333), 2.021(100)(044), 1.906(8)(006,244) and 1.429(7)(008). The crystal structure was solved and refined from the single-crystal X-ray diffraction data of synthetic Ni8Pd3As4. The relation between natural and synthetic nipalarsite is illustrated by an electron back-scattered diffraction study of natural nipalarsite. The density calculated on the basis of the empirical formula of nipalarsite is 9.60 g.cm–3. The mineral name corresponds to the three main elements: Ni, Pd and As.

Verbeekite, ideally PdSe2, monoclinic with space-group choices C2/m, C2 or Cm; a = 6.659(7), b = 4.124(5), c = 4.438(6) Å, ß = 92.76(3)°, V = 121.7(4) Å3; a:b:c = 1.6147:1:1.0761, Z = 2, is a new, very rare, primary mineral, intimately associated with secondary oosterboschite {(Pd,Cu)7Se5}, from the Musonoi Cu-Co-Mn-U mine, near Kolwezi, Shaba Province, Democratic Republic of Congo. Additional associated minerals are Cu- and Pd-bearing trogtalite {(Co,Cu,Pd)Se2}, Se-bearing digenite and Se-bearing covellite. The strongest five lines of the X-ray powder-diffraction pattern {d in Å (I) (hkl)} are: 4.423(30)(001), 3.496 (30)(110), 2.718(100)(111), 1.955(50)(310 and 1.896(50)(12). The mineral has also been identified, as a single anhedral 25 µm-sized grain, from Hope's Nose, Torquay, Devon, England where it is associated with native gold, chrisstanleyite Ag2Pd3Se4, oosterboschite(?), unnamed Pd2HgSe3 and cerussite. At Musonoi, altered verbeekite grains do not exceed 200 µm in size and are anhedral, black, with a black streak and a metallic lustre. The mineral is opaque, brittle, has an uneven fracture, and lacks discernible cleavage. The VHN5 ranges 490–610, mean 550 kp/mm2 (2 indentations), roughly approximating a Mohs' hardness of 5Ý. Dcalc. = 7.211 g/cm3 for the ideal formula. Electron-microprobe analyses (mean of 4 spot analyses) yielded Pd 39.6, Cu 0.5, Se 58.8, total 98.9 wt.%. The empirical formula is (Pd0.99Cu0.02)σ1.01Se1.99, based on Pd+Cu+Se = 3. In plane-polarized reflected light, the mineral is a nondescript grey and is neither pleochroic nor perceptibly bireflectant. Anisotropy is moderate with rotation tints in varying shades of brown. Reflectance spectra and colour values are tabulated. The name honours Dr Théodore Verbeek (1927–1991) who was the first geoscientist to study the Musonoi palladium mineralization in the Democratic Republic of Congo (1955–1967) and who co-discovered this new mineral phase.

Feinglosite, the zinc analogue of arsenbrackebuschite, was found lining a cavity in a sample of massive chalcocite from Tsumeb, Namibia. In this cavity it is associated with wulfenite, anglesite and goethite. The mean of seven electron-microprobe analyses (wt.%) is: PbO 61.4, ZnO 7.3, FeO 1.8, As2O5 22.1, SO3 5.3, H2O (by difference) [2.1], total = [100.00]%, leading to the ideal formula: Pb2(Zn,Fe)[(As,S)O4]·H2O. Feinglosite is monoclinic, space group P21 or P21/m, a 8.973(6), b 5.955(3), c 7.766(6) Å, β 112.20(6)°, with Z = 2. The strongest five reflections of the X-ray powder diffraction pattern are [d in Å (I) (hkl)]: 4.85 (50) (110), 3.246 (100) (112), 2.988 (60) (301), 2.769 (60) (300/211), 2.107 (50) (321). The mineral is pale olive-green, transparent, sectile, and has a white streak and adamantine lustre. It overgrows clusters of goethite crystals and forms globular microcrystalline aggregates up to 0.5–0.75mm in size. The hardness on Mohs' scale is 4–5: the mean micro-indentation hardness is 263 at VHN100. Its calculated density is 6.52 g cm−3. The mineral is pale brownish grey in reflected light (when compared with goethite). Visible spectrum reflectance data are presented. Feinglosite is named for Mark N. Feinglos who first recognised the mineral on a specimen in his collection.

Chrisstanleyite, Ag2Pd3Se4, is a new mineral from gold-bearing carbonate veins in Middle Devonian limestones at Hope's Nose, Torquay, Devon, England. It is associated with palladian and argentian gold, fischesserite, clausthalite, eucairite, tiemannite, umangite, a Pd arsenide-antimonide (possibly mertieite II), cerussite, calcite and bromian chlorargyrite. Also present in the assemblage is a phase similar to oosterboschite, and two unknown minerals with the compositions, PdSe2 and HgPd2Se3. Chrisstanleyite occurs as composite grains of anhedral crystals ranging from a few µm to several hundred µm in size. It is opaque, has a metallic lustre and a black streak, VHN100 ranges from 371–421, mean 395 kp/mm2 (15 indentations), roughly approximating to a Mohs hardness of 5. Dcalc = 8.308 g/cm3 for the ideal formula with Z = 2. In plane-polarised reflected light, the mineral is very slightly pleochroic from very light buff to slightly grey-green buff; is weakly bireflectant and has no internal reflections. Bireflectance is weak to moderate (higher in oil). Anisotropy is moderate and rotation tints vary from rose-brown to grey-green to pale bluish grey to dark steel-blue. Polysynthetic twinning is characteristic of the mineral. Reflectance spectra and colour values are tabulated. Very little variation was noted in eleven electron-microprobe analyses on five grains, the mean is: Ag 25.3, Cu 0.17, Pd 37.5, Se 36.4, total 99.37 wt.%. The empirical formula (on the basis of ∑M + Se = 9) is (Ag2.01Cu0.02)∑2.03 Pd3.02Se3.95, ideally Ag2Pd3Se4. Chrisstanleyite is monoclinic, a 6.350(6), b 10.387(4), c 5.683(3) Å β 114.90(5)°, space group P21/m (11) or P21(4). The five strongest X-ray powder-diffraction lines [d in Å (I)(hkl)] are: 2.742 (100) (–121), 2.688 (80) (–221), 2.367 (50) (140), 1.956 (100) (–321,150) and 1.829 (30) (–321, 042). The name is in honour of Dr Chris J. Stanley of The Natural History Museum in London. The mineral and its name have been approved by the Commission on New Minerals and Mineral Names of the International Mineralogical Association.

A REE-bearing fluorosilicate from the Tommot REE-Nb deposit in Yakutia, Russia, described without a name in 1966, is characterized here as a new species, proshchenkoite-(Y), of the vicanite group of borosilicates. Wavelength-dispersive electron probe analyses gave the following empirical formula: Y3.70REE7.54Ca1.55Na1.16Mn0.77Th0.10Pb0.01)Σ14.83(Fe2+0.83Mn0.15Ti0.02)Σ1.00Ca1.00(P0.70Si0.26As0.04)Σ1.00Si0.26B3.20(O34.55F13.45)Σ48. Boron was analysed with a nuclear microprobe method based on the nuclear reaction 11B(p,α)2α. The simplified formula is (Y,REE,Ca,Mn)15(Fe2+,Mn)Ca(P,Si)Si6B3O34F14. The mineral is trigonal, R3m, with a = 10.7527(7) Å, c = 27.4002(18) Å, V = 2743.6(6) Å 3, Z = 3. The crystal structure was refined to Rl = 0.042 for 1819 observed reflections. Proshchenkoite-(Y) is isostructural with okanoganite-(Y), vicanite-(Ce) and hundholmenite-(Y), and the differences in site occupancies are discussed. The strongest six reflections of the X-ray powder-diffraction pattern [dobs in Å, (I), (hkl)] are: 4.441, (36), (202); 3.144, (77), (214); 3.028, (45). (009); 2.968, (100), (027); 1.782, (32), (330); and 1.713, (32), (1.2.14). The mineral is optically uniaxial (—) with ω 1.734(2) and 8 1.728(2). The Mohs hardness is about 5; density measured on material subject to incipient metamictization is 4.72 g/cm3, as compared to Dcalc = 4.955 g/cm3.

The result of electron microprobe analyses of alleged okanoganite-(Y) from the type locality in Okanogan County, Washington, USA, is also presented. We find here also that P > Si at one of the sites, whereas the analytical data of Boiocchi et al. (2004) indicate Si > P. Consequently, the mineral we have analysed is the P analogue of okanoganite-(Y), another new species.

Petewilliamsite, ideally (Ni,Co)30(As2O7)15, monoclinic, space group C2, a = 33.256(5), b = 8.482(1), c = 14.191(2) Å, ß = 104.145(3)°, V = 3881.6(11) Å3, a:b:c = 3.9209:1:1.6731, Z = 2, is a new mineral found on a single nickeline-veined quartz specimen from Johanngeorgenstadt, Saxony, Germany. The mineral possesses a pronounced subcell-supercell: a (subcell) = 1/5 a (supercell); b (subcell) = b (supercell); c (subcell) = 1/3 c (supercell), and the strongest six lines of the X-ray powder-diffraction pattern are [d in Å (I) (hkl)]: 4.235(30)(020) ; 3.118(100)(513, 023); 3.005(60); 2.567(50); 1.637(50)(536 ); 1.507(30b)(553, ). It occurs predominantly as scattered patches of mm-sized aggregates which are intimately associated with varicoloured xanthiosite; additional associations include bunsenite, aerugite, rooseveltite, native bismuth, paganoite and two undefined arsenates. Subhedral equant crystals with rounded faces are intimately intergrown in 1 mm-sized aggregates and individual grains do not exceed 0.5 mm in maximum diameter. The average crystal size is variable from 20 μm to 0.3 mm. The colour varies from dark violet-red to dark brownish-red and the streak is pale reddish-brown to pale purplish-brown. Crystals are translucent, brittle, vitreous, and do not fluoresce under ultraviolet light. The mineral shows neither twinning nor cleavage, has an uneven fracture, and the calculated density (for the empirical formula) is 4.904 g/cm3. Electron-microprobe analyses gave NiO 19.45, CoO 18.39, CuO 3.40, CaO 0.17, FeO 0.04, As2O5 60.32, total 101.77 wt.%. The empirical formula, derived from crystal-structure analysis and electron-microprobe analyses, is (Ni14.662+Co13.822+Cu2.412+Ca0.17Fe0.032+)Σ31.09(As1.975+O7)15, based on O = 105 atoms per formula unit (a.p.f.u.). In reflected plane-polarized light in air, petewilliamsite is dark grey with orange to spectral (multicoloured) internal reflections and no obvious bireflectance, anisotropy or pleochroism. Measured reflectance values in air are tabulated; the index of refraction calculated at 589 nm is 1.88. The mineral name honours Professor Peter (‘Pete’) Allan Williams of the University of Western Sydney, New South Wales, Australia, for his contributions to the study of secondary minerals.

The crystal structure of petewilliamsite has been solved by direct methods and refined on the basis of F2 using 9212 unique reflections measured with Mo-Kα X-radiation on a diffractometer equipped with a CCDbased detector. The final R1 was 7.68%, calculated for 1273 observed reflections. The structure contains 15 symmetrically distinct As5+ cations, each of which is tetrahedrally coordinated by four O atoms, and pairs of these AsO4 tetrahedra share a vertex which results in As2O7 pyroarsenate groups that are in layers parallel to (010). The structure also has 16 distinct transition-metal M (M: Ni,Co) sites of which there are one tetrahedral, four square bipyramidal, and 11 octahedral arrangements. Adjacent pyroarsenate groups are linked through bonds to M cations. The structure of petewilliamsite is not closely related to other naturally occurring arsenates and it is the first pyroarsenate mineral.

A detailed crystal-chemical study of the complex layered silicate molybdophyllite was conducted using single-crystal X-ray diffraction (XRD) methods, supplemented by powder XRD, infrared (IR) and Raman spectroscopic studies, chemical analyses by energy-dispersive spectrometry (EDS) on a scanning electron microscope (SEM), and electron probe microanalysis (EPMA). The results, based on several samples from both Långban and Harstigen, Filipstad, Sweden, show that the crystal structure of molybdophyllite has an order-disorder (OD) character. The latter is especially evident in specimens from Långban which display a complex diffraction pattern characterized by the simultaneous presence of sharp spots, diffuse reflections and continuous streaks. The sharp reflections define the unit cell of the family structure (a = 3.124, c = 41.832 Å, space group R32). Two main polytypes (maximum degree of order structures) are indicated by the OD approach: a trigonal one and a monoclinic one; the latter polytype is the most common in the samples that were studied and has space group C2, with a = 16.232(6), b = 9.373(2), c = 14.060(3) Å, b = 97.36(4)º and V = 2121.5(10) Å3.

The crystal structure determination [R1 = 0.096], together with the EPMA, IR and Raman data, reveal that molybdophyllite is built up by a regular alternation of complex layers with a composition {Mg9[Si10O28(OH)8][OPb4]2}6+ and simple layers with a composition [(CO3)3·H2O]6–, leading to the ideal crystal-chemical formula Pb8Mg9[Si10O28(OH)8|O2|(CO3)3]·H2O (Z = 2).

This contribution is mainly devoted to the results obtained for molybdophyllite sensu stricto, but new data for britvinite [i.e. 'molybdophyllite-18 Å'] are also presented and its modular relationship with molybdophyllite is discussed.

Silvialite, ideally Ca4Al6Si6O24SO4, is tetragonal, I4/m, Z = 2, with a = 12.160(3), c = 7.560(1) Å, V = 1117.9(8) Å3, c:a = 0.6217:1, ω = 1.583, ε = 1.558 (uniaxial negative), Dm = 2.75 g/cm3, Dcalc = 2.769 g/cm3 and H (Mohs) = 5.5. It is transparent and slightly yellow, has a good {100} cleavage, chonchoidal fracture, white streak and a vitreous lustre. It occurs in upper-mantle garnet-granulite xenoliths hosted by olivine nephelinite, from McBride Province, North Queensland, Australia. The empirical formula, derived from electron-microprobe analysis, is (Na1.06Ca2.86)(Al4.87Si7.13)O24 [(SO4)0.57(CO3)0.41]. Crystal-structure refinement shows disordered carbonate and sulfate groups along the fourfold axis. Silvialite is a primary cumulate phase precipitated from alkali basalt at 900–1000°C and 8–12 kbar under high fSO2 and fO2. The name silvialite, currently used in literature to describe the sulfate analogue of meionite, was suggested by Brauns (1914).

Agmantinite, ideally Ag2MnSnS4, is a new mineral from the Uchucchacua polymetallic deposit, Oyon district, Catajambo, Lima Department, Peru. It occurs as orange–red crystals up to 100 μm across. Agmantinite is translucent with adamantine lustre and possesses a red streak. It is brittle. Neither fracture nor cleavage were observed. Based on the empirical formula the calculated density is 4.574 g/cm3. On the basis of chemically similar compounds the Mohs hardness is estimated at between 2 to 2½. In plane-polarised light agmantinite is white with red internal reflections. It is weakly bireflectant with no observable pleochroism with red internal reflections. Between crossed polars, agmantinite is weakly anisotropic with reddish brown to greenish grey rotation tints. The reflectances (Rmin and Rmax) for the four standard wavelengths are: 19.7 and 22.0 (470 nm); 20.5 and 23.2 (546 nm); 21.7 and 2.49 (589 nm); and 20.6 and 23.6 (650 nm), respectively.

Agmantinite is orthorhombic, space group P21nm, with unit-cell parameters: a = 6.632(2), b = 6.922(2), c = 8.156(2) Å, V = 374.41(17) Å3, a:b:c 0.958:1:1.178 and Z = 2. The crystal structure was refined to R = 0.0575 for 519 reflections with I > 2σ(I). Agmantinite is the first known mineral of ${M}_{\rm 2}^{\rm I} $MIIMIVS4 type that is derived from wurtzite rather than sphalerite by ordered substitution of Zn, analogous to the substitution pattern for deriving stannite from sphalerite. The six strongest X-ray powder-diffraction lines derived from single-crystal X-ray diffraction data [d in Å (intensity)] are: 3.51 (s), 3.32 (w), 3.11 (vs), 2.42 (w), 2.04 (m) and 1.88 (m). The empirical formula (based on 8 apfu) is (Ag1.94Cu0.03)Σ1.97(Mn0.98Zn0.05)Σ1.03Sn0.97S4.03.The crystal structure-derived formula is Ag2(Mn0.69Zn0.31)Σ1.00SnS4 and the simplified formula is Ag2MnSnS4.

The name is for the composition and the new mineral and mineral name have been approved by the International Mineralogical Association Commission on New Minerals, Nomenclature and Classification (IMA2014-083).

Vymazalováite, Pd3Bi2S2 is a new platinum-group mineral discovered in the Komsomolsky mine of the Talnakh deposit, Noril'sk district, Russia. It forms small (from a few μm to 20–35 µm) inclusions or euhedral grains in intergrowths of polarite, sobolevskite, acanthite and unnamed (Pd,Ag)5BiS2 in aggregates (up to ~200 µm) in galena and rarely in chalcopyrite. It occurs with telargpalite, cooperite, braggite, vysotskite, sopcheite, stibiopalladinite, sobolevskite, moncheite, kotulskite, malyshevite, insizwaite, Au-bearing silver and the newly described mineral kravtsovite (PdAg2S) in association with pyrite, chalcopyrite and galena in vein-disseminated mineralization in skarn rocks. Synthetic vymazalováite is brittle; it has a metallic lustre and a grey streak. In plane-polarized reflected light, vymazalováite is creamy grey and appears slightly brownish against galena in the assemblage with chalcopyrite. It exhibits no internal reflections. Average reflectance values in air for natural and synthetic vymazalováite are (R natural, R synthetic in %) are: 46.35, 45.7 at 470 nm, 47.65, 47.45 at 546 nm, 48.5, 48.2 at 589 nm and 49.5, 49.0 at 650 nm. Seven electron probe micro-analyses of vymazalováite give an average composition: Pd 40.42, Bi 49.15, Ag 0.55, Pb 1.02, S 7.77 and Se 0.26, total 99.17 wt.%, corresponding to the empirical formula Pd3.05(Bi1.89Ag0.04Pb0.04)Σ1.97(S1.95Se0.03)Σ1.98 based on a total of 7 atoms per formula unit. The simplified formula is Pd3Bi2S2. The mineral is cubic, space group I213, with a = 8.3097(9) Å, V = 573.79(1) Å3 and Z = 4. The density calculated on the basis of the empirical formula and cell dimensions of synthetic vymazalováite is 9.25 g/cm3. The strongest lines in the powder X-ray diffraction pattern of synthetic vymazalováite [d in Å (I) (hkl)] are: 4.15(32)(200), 2.93(78)(220), 2.40(100)(220), 2.08(53)(400), 1.695(34)(422), 1.468(35)(440) and 1.252(31)(622). The structural identity of natural vymazalováite with synthetic Pd3Bi2S2 was confirmed by electron back-scatter diffraction measurements on the natural sample. This new mineral honours Dr Anna Vymazalová of the Czech Geological Survey, Prague.

Norilskite, (Pd,Ag)7Pb4 is a new platinum-group mineral discovered in the Mayak mine of the Talnakh deposit, Russia. It forms anhedral grains in aggregates (up to ∼400 μm) with polarite, zvyagintsevite, Pd-rich tetra-auricupride, Pd-Pt bearing auricupride,Ag-Au alloys, (Pb,As,Sb) bearing atokite, mayakite, Bi-Pb-rich kotulskite and sperrylite in pentlandite, cubanite and talnakhite. Norilskite is brittle, has a metallic lustre and a grey streak. Values of VHN20 fall between 296 and 342 kg mm–2, with a mean valueof 310 kg mm–2, corresponding to a Mohs hardness of ∼4. In plane-polarized light, norilskite is orange-brownish pink, has moderate to strong bireflectance, orange-pink to greyish-pink pleochroism, and strong anisotropy; it exhibits no internal reflections. Reflectancevalues of norilskite in air (Ro, Re' in %) are: 51.1, 48.8 at 470 nm, 56.8, 52.2 at 546 nm, 59.9, 53.5 at 589 nm and 64.7, 55.5 at 650 nm. Sixteen electronmicroprobe analyses of natural norilskite gave an average composition: Pd 44.33, Ag 2.68, Bi 0.33 and Pb 52.34, total99.68 wt.%, corresponding to the empirical formula (Pd6.56Ag0.39)∑6.95(Pb3.97Bi0.03)∑4.00 based on 4 Pb + Bi atoms; the average of eight analyses on synthetic norilskite is: Pd 42.95, Ag 3.87 and Pb 53.51, total 100.33wt.%, corresponding to (Pd6.25Ag0.56)∑6.81Pb4.00. The mineral is trigonal, space group P3121, with a = 8.9656(4), c = 17.2801(8) Å, V = 1202.92(9) Å3 and Z = 6. The crystalstructure was solved and refined from the powder X-ray diffraction data of synthetic (Pd,Ag)7Pb4. Norilskite crystallizes in the Ni13Ga3Ge6 structure type, related to nickeline. The strongest lines in the powder X-ray diffraction patternof synthetic norilskite [d in Å (I) (hkl)] are: 3.2201(29)(023,203), 2.3130(91)(026,206), 2.2414(100)(220), 1.6098(28)(046,406), 1.3076(38)(246,462), 1.2942(18)(600), 1.2115(37)(22.12,12.13), 0.9626(44) (06.12,60.12). The mineral is named for the locality, the Noril'sk district in Russia.