In this issue
This New Mineral Names has entries for 15 new minerals, including antipinite, anzaite-(Ce), bettertonite, bobshannonite, calcinaksite, khvorovite, leguernite, lukkulaisvaaraite, minjiangite, möhnite, moraskoite, nickelpicromerite, pilawite-(Ce), ralphcannonite, and yeomanite.
Antipinite*
N.V. Chukanov, S.M. Aksenov, R.K. Rastsvetaeva, K.A. Lysenko, D.I. Belakovskiy, G. Färber, G. Möhn and K.V. Van (2015) Antipinite, KNa3Cu2(C2O4)4, a new mineral species from a guano deposit at Pabellón de Pica, Chile. Mineralogical Magazine, 79(5), 1111–1121.Chukanov N.V., Aksenov S.M., Rastsvetaeva R.K., Lysenko K.A., Belakovskiy D.I., Färber G., Möhn G., Van K.V. , 2015"Antipinite, KNa3Cu2(C2O4)4, a new mineral species from a guano deposit at Pabellón de Pica, Chile" Mineralogical Magazine, vol. 79, no. 5, p. 1111–1121.
Antipinite (IMA 2014-027), ideally KNa3Cu2(C2O4)4, was discovered in the guano deposit at the lower part of the northern slope of Pabellón de Pica Mountain, Tarapacá Region, Chile. The new mineral honors Mikhail Yuvenal’evich Antipin (1951–2013), a Russian specialist in the crystallography and crystal chemistry of organometallic and coordination compounds. Antipinite occurs in association with halite, salammoniac, chanabayaite, and joanneumite. The host gabbro consists of amphibole, plagioclase, minor clinochlore, and accessory chalcopyrite. Antipinite forms isometric and short prismatic crystals up to 0.1×0.1×0.15 mm, and random aggregates up to 0.6 mm across. The new mineral is blue, translucent, with pale blue streak and a vitreous luster. It is brittle, with a Mohs hardness ~2. The cleavage is medium in three directions, which were not determined. Dmeas = 2.53(3) and Dcalc = 2.549 g/cm3. Antipinite does not fluoresce under UV radiation. It is optically biaxial (+), α = 1.432(2), β = 1.530(2), and γ = 1.698(5) (λ = 589 nm); 2Vmeas = 75(10)°; 2Vcalc = 82°. Dispersion of optical axes is strong, r < ν. The mineral is strongly pleochroic: Z (blue) > Y (light blue) > X (colorless). Antipinite dissolves in water, and its concentrated aqueous solution has a pH of 9. The main bands of the IR spectrum of antipinite (cm–1) are: weak bands over 1800 (combination modes), 1500–1750 (asymmetric stretching vibrations of carboxylate groups), 1280–1490 (their symmetric stretching vibrations), 780–900 (in-plane bending vibrations of the carboxylate groups, possibly combined with C-C stretching vibrations), 495–557 (out-of-plane bending vibrations of the carboxylate groups). No absorption bands associated with H2O molecules, C-H bonds,
Anzaite-(Ce)*
A.R. Chakhmouradian, M.A Cooper, L. Medici, Y.A. Abdu and Y.S. Shelukhina (2015) Anzaite-(Ce), a new rare-earth mineral and structure type from the Afrikanda silicocarbonatite, Kola Peninsula, Russia. Mineralogical Magazine, 79(5), 1231–1244.Chakhmouradian A.R., Cooper M.A, Medici L., Abdu Y.A., Shelukhina Y.S. , 2015"Anzaite-(Ce), a new rare-earth mineral and structure type from the Afrikanda silicocarbonatite, Kola Peninsula, Russia" Mineralogical Magazine, vol. 79, no. 5, p. 1231–1244.
Anzaite-(Ce) (IMA 2013-004), ideally
Bettertonite*
I.E. Grey, A.R. Kampf, J.R. Price and C.M. Macrae (2015) Bettertonite, [Al6(AsO4)3(OH)9(H2O)5]·11H2O, a new mineral from the Penberthy Croft mine, St. Hilary, Cornwall, UK, with a structure based on polyoxometalate clusters. Mineralogical Magazine, 79(7), 1849–1858.Grey I.E., Kampf A.R., Price J.R., Macrae C.M. , 2015"Bettertonite, [Al6(AsO4)3(OH)9(H2O)5]·11H2O, a new mineral from the Penberthy Croft mine, St. Hilary, Cornwall, UK, with a structure based on polyoxometalate clusters" Mineralogical Magazine, vol. 79, no. 7, p. 1849–1858.
A new mineral bettertonite (IMA 2014-074), ideally [Al6(AsO4)3(OH)9(H2O)5]·11H2O, was discovered at the Penberthy Croft mine in ~1.5 km from the village of Goldsithney, St. Hilary, Cornwall, England, U.K. (50.1414°N 5.4269°W). The mine is well known as a source of rare secondary CuPbFe arsenates and was classified in 1993 as an SSSI (Site of Special Scientific Interest). Bettertonite occurs in quartz veins closely associating with arsenopyrite, chamosite, liskeardite, pharmacoalumite, pharmacosiderite and minor brochantite, chalcopyrite and cassiterite. Much of supergene alteration is post mining. The new mineral along with liskeardite was probably formed from leaching and the replacement of Al to Fe in pharmacosiderite, Bettertonite forms bright white, lustrous, ultra-thin (sub-micrometer) blades, sprays and laths with lateral dimensions <20 μm, or their radiating groups that line and infill interconnecting and isolated cavities (14 mm) in quartz and chamosite. The laths are flattened on {010}; other forms are {010}, {100}, and {001}. Bettertonite is translucent with a white streak and a vitreous to pearly or silky luster. The cleavage on {010} is perfect. The density was not measured due to the thinness of the crystals; Dcalc = 2.02 g/cm3. The mineral is nonpleochroic, optically biaxial (+) with α = 1.511, β = 1.517, γ = 1.523 (white light), 2Vcalc = 60.2°; X = c, Y = b, Z = a. The average of 4 electron probe WDS analyses [wt% (range)] is: Al2O3 35.8 (34.5–36.1), Fe2O3 2.45 (1.93–2.82), As2O5 36.5 (35.6–37.7), SO3 2.19 (1.18–2.60), Cl 0.56 (0.29–0.89), O=Cl2 0.13, total 77.47. Normalized to a total of 100% when combined with the H2O calculated based on structure analysis: Al2O3 29.5, Fe2O3 2.0, As2O5 30.1, SO3 1.8, Cl 0.5, H2O 36.2. The empirical formula, based on 9 (Al+Fe+As+S) pfu is Al5.86Fe0.26(AsO4)2.65(SO4)0.23 (OH)9.82Cl0.13(H2O)15.5. The strongest lines in the powder X-ray diffraction pattern are [d Å (I%; hkl)]: 13.65 (100; 011), 13.51 (50; 020), 7.805 (50; 031), 7.461 (30; 110), 5.880 (20; 130), 3.589 (20; 202); 2.857 (14; 182). The monoclinic unit-cell parameters refined in space group P21/c from the powder X-ray data are a = 7.788(3), b = 26.957(7), c = 15.925(8) Å, β = 93.9(1)°, V = 3336 Å3. The refinement of single crystal data collected at 100 K on the microfocus beamline MX2 at the Australian Synchrotron (λ = 0.71073 Å) on a rectangular lath (20×10×1 μm) yielded R1 = 0.083 for 2164 observed [I > 2σ(I)] reflections. The singlecrystal unit-cell parameters are: a = 7.773(2), b = 26.991(5), c = 15.867(3) Å, β = 94.22(3)°, V = 3319.9 Å3, Z = 4. Bettertonite is a natural example of a polyoxometalate (POM) compounds. It has a heteropolyhedral layered structure, with the layers parallel to (010). The layers comprise hexagonal rings of edge-shared AlO6 octahedra that are interconnected by sharing corners with AsO4 tetrahedra. The layers are strongly undulating and their stacking produces large channels along [100] that are filled with water molecules. These polyoxometalate clusters, of composition [AsAl6O11(OH)9(H2O)5]8–, are interconnected along [100] and [001] by corner-sharing with other AsO4 tetrahedra. The mineral honors John Betterton (b. 1959) a museum geologist/mineralogist at Haslemere Educational Museum, Haslemere, Surrey, U.K., for his extensive contributions to the characterization of minerals from the Penberthy Croft mine. Cotype specimens are deposited in the Museum Victoria, Melbourne, Victoria, Australia, and in the Natural History Museum, London, U.K. D.B.
Bobshannonite*
E. Sokolova, F. Cámara, Y.A. Abdu, F.C. Hawthorne, L. Horváth and E. Pfenninger-Horváth (2015) Bobshannonite, Na2KBa(Mn, Na)8(Nb, Ti)4(Si2O7)4O4(OH)4(O, F)2, a new TS-block mineral from Mont Saint-Hilaire, Québec: Description and crystal structure. Mineralogical Magazine, 79(7), 1791–1811.Sokolova E., Cámara F., Abdu Y.A., Hawthorne F.C., Horváth L., Pfenninger-Horváth E. , 2015"Bobshannonite, Na2KBa(Mn, Na)8(Nb, Ti)4(Si2O7)4O4(OH)4(O, F)2, a new TS-block mineral from Mont Saint-Hilaire, Québec: Description and crystal structure" Mineralogical Magazine, vol. 79, no. 7, p. 1791–1811.
The new mineral bobshannonite (IMA 2014052), ideally Na2KBa(Mn, Na)8(Nb, Ti)4(Si2O7)4O4(OH)4(O, F)2, was discovered in the pegmatite from a blast pile at the Poudrette quarry, Mont Saint-Hilaire, Québec, Canada. The type specimen is 2.5×2.3×2 cm and consists mostly (~90%) of sérandite. Orange-brown blocky crystals of bobshannonite up to 0.51 mm are perched on sérandite and albite. Other associated minerals are epididymite (rich), catapleiite, aegirine (2 generations), kupletskite, rhodochrosite, and rhabdophane-(Ce) and undetermined botryoidal Mn oxide. The mineral is of hydrothermal origin. The main forms of euhedral crystals of bobshannonite are {001}, {110}, {110}, and {010}. The mineral is vitreous to frosty, transparent to translucent pale brown (in small fragments) to orange brown with a very pale brown streak and hackly fracture. Cleavage is perfect on {001} and no parting was observed. It does not fluoresce under cathode or UV rays. The mineral is brittle with a Mohs hardness ~4. The density was not measured; Dcalc = 3.787 g/cm3. Crystals of bobshannonite are extensively twinned and do not extinguish in cross-polarized light. That did not allow to obtain data on optical properties. The mineral is non pleochroic in the cleavage plain, but change color from colorless to brown in other sections. The FTIR and Raman spectra show a strong peak at 3610 with a weak shoulder at 3655 cm–1 assigned to the stretching vibrations of OH groups. A strong peak at 901 cm-1 and medium- to low-intensity peaks at 1038, 970, 716, and 680 cm-1 on the Raman spectrum may be assigned to Si–O stretching vibrations of the Si2O7 groups. Peaks at 608, 580, 510, and 410 cm-1 correspond to bending vibrations of Si2O7 groups and those at 341, 310, 240, 207, and 143 cm-1 to the lattice modes. The average of 9 electron probe WDS analysis (ranges are not given) is (wt%): Ta2O5 0.52, Nb2O5 19.69, TiO2 5.50, SiO2 26.31, Al2O3 0.06, BaO 7.92, ZnO 1.02, FeO 0.89, MnO 26.34, MgO 0.06, Rb2O 0.42, K2O 2.38, Na2O 4.05, F 0.70, H2O (calculated using structure data) 1.96, O=F2 0.29, total 97.53. The empirical formula based on 38 (O+F) is Na1.89(K0.93Rb0.08)∑1.01Ba0.95(Mn6.85Na0.52Zn0.23
References cited
Sokolova, E. (2006) From structure topology to chemical composition. I. Structural hierarchy and stereochemistry in titanium disilicate minerals. Canadian Mineralogist, 44(6), 1273–1330.Sokolova E. , 2006"From structure topology to chemical composition. I. Structural hierarchy and stereochemistry in titanium disilicate minerals" Canadian Mineralogist, vol. 44, no. 6, p. 1273–1330.
Calcinaksite*
N.V. Chukanov, S.M. Aksenov, R.K. Rastsvetaeva, G. Blass, D.A. Varlamov, I.V. Pekov, D.I. Belakovskiy and V.V. Gurzhiy (2015) Calcinaksite, KNaCa(Si4O10)H2O, a new mineral from the Eifel volcanic area, Germany. Mineralogy and Petrology, 109, 397–404.Chukanov N.V., Aksenov S.M., Rastsvetaeva R.K., Blass G., Varlamov D.A., Pekov I.V., Belakovskiy D.I., Gurzhiy V.V. , 2015"Calcinaksite, KNaCa(Si4O10)H2O, a new mineral from the Eifel volcanic area, Germany" Mineralogy and Petrology, vol. 109, p. 397–404.
Calcinaksite (IMA 2013-081), ideally KNaCa(Si4O10)2·H2O, is a new mineral found in a xenolith of metamorphosed carbonate-rich rock from the southern lava flow of the Bellerberg volcano, Eastern Eifel region, Rheinland-Pfalz, Germany. It is named for its chemical composition and by analogy with manaksite and fenaksite, Mn and Fe end-members. The new mineral occurs in association with wollastonite, gehlenite, brownmillerite, calcio-olivine, quartz, aragonite, calcite, jennite, tobermorite, and ettringite. Calcinaksite forms clusters of subhedral prismatic crystals that are elongated along a, up to 1 cm long and embedded with wollastonite, gehlenite, and other calcium silicates. It is colorless to light gray, brittle, with a Mohs hardness of 5. Calcinaksite has two perfect cleavages on {001} and {010}. Dmeas = 2.62(2) and Dcalc = 2.623 g/cm3. Calcinaksite does not fluoresce in both UV and cathode rays. It is biaxial (+), with α = 1.542(2), β = 1.550(2), γ = 1.565(2) (λ = 589 nm), 2Vmeas = 75(10)°; 2Vmeas= 73°; YΛa =42°, Z Λa ≈ 90°. Dispersion of optical axes is medium, r < ν. The main bands of the IR spectrum are (cm–1, s = strong, w = weak, sh = shoulder): 3540, 3340w, 3170w (O-H stretching vibrations of H2O molecules), 1654w (bending vibrations of H2O molecules), 1122, 1075sh, 1055sh, 1041s, 1013, 971s (Si-O stretching vibrations), 775w, 679, 624, 597, 523 (bending vibrations of the tubular silicate radical Si4O10), 480sh, 456, 421s, 395w (lattice modes involving Si-O-Si bending and Ca-O stretching vibrations). The average of 18 electron probe EDS analyses is [(wt% (range)]: SiO2 61.46 (60.83–62.08), FeO 0.59 (0–1.11), CaO 15.04 (14.15–15.66), K2O 12.01 (11.21–12.64), Na2O 6.69 (6.22–7.31), H2O 4.9 (two measurements 4.72 and 5.05 by the Alimarin method), total 100.69. The formula calculated based on 11 O atoms pfu is: K0.99Na0.84Ca1.04 Fe0.03Si3.98O11. The strongest lines of the X-ray powder diffraction pattern [d Å (I%; hkl)] are: 3.431 (70;
Khvorovite*
L.A. Pautov, A.A. Agakhanov, E.V. Sokolova, F.C. Hawthorne, V.Yu. Karpenko, O.I. Siidra, V.K. Garanin and Y.A. Abdu (2015) Khvorovite,
Khvorovite (IMA 2014-050), ideally
Leguernite*
A. Garavelli, D. Pinto, D. Mitolo and L. Bindi (2015) Leguernite, Bi12.67O14(SO4)5, a new Bi oxysulfate from the fumarole deposit of La Fossa crater, Vulcano, Aeolian Islands, Italy. Mineralogical Magazine, 78(7), 1629–1645Garavelli A., Pinto D., Mitolo D., Bindi L. , 2015"Leguernite, Bi12.67O14(SO4)5, a new Bi oxysulfate from the fumarole deposit of La Fossa crater, Vulcano, Aeolian Islands, Italy" Mineralogical Magazine, vol. 78, no. 7, p. 1629–1645.
Leguernite (IMA 2013-051), ideally Bi12.67O14(SO4)5, is a new mineral found at La Fossa crater, Vulcano, Aeolian Islands, Italy. The mineral was found in a cavity of a volcanic rock sample from the walls of the high-temperature fumarole FF (T = 600 °C) closely associated with anglesite, balicšunicite, and an unknown Bi sulfate. Other associated minerals include lillianite, galenobismutite, bismoclite, Cd-rich sphalerite, Cd-rich wurtzite, pyrite, and pyrrhotite. It occurs as fibrous aggregates of needle-shaped crystals up to 0.4 × 0.01 mm. Leguernite is colorless to white, transparent with white streak and subadamantine luster. It is brittle, shows no cleavage, parting, or fractures. No twinning was observed. Hardness, density and refractive indices were not measured due to size and paucity of material; Dcalc = 7.375 g/cm3. The mineral does not fluoresce under UV light. The Raman spectrum shows peaks in the region 600–1200 cm–1 (SO4 stretching modes) and 400–600 cm–1 (SO4 bending modes). Most of the bands in the region 100–400 cm–1 are due to the Bi-O lattice vibrations. A peak at 2430 cm–1 remains unassigned. No peaks confirming the presence of OH or H2O groups were observed.. The average of 9 electron probe EDS analyses on different crystals belonging to the same needle aggregate is [wt% (range)]: SO3 11.06 (10.76–11.29), Bi2O3 78.57 (75.80–80.03), PbO 0.91 (0.36–1.63) total 90.54. This gives the empirical formula (Bi12.40Pb0.15)∑12.55 S5.08O34 based on 34 anions pfu. The strongest lines in the X-ray powder-diffraction pattern [d Å (I%; hkl)] are: 3.220 (100; 013), 3.100 (95; 311), 2.83 (30; 020), 2.931 (25; 302), 2.502 (25; 304), 2.035 (20; 322), 1.875 (20; 324), and 5.040 (15; 110). The unitcell parameters refined from powder-diffraction data are: a = 11.250(5), b = 5.654(2), c = 11.906(5) Å, α = 99.13(5)°, and V = 747.8 Å3. Single-crystal X-ray diffraction data collected on a crystal of size 0.260×0.034×0.016 mm refined to R1 = 0.0766 for 2372 unique I ≥ 4σ(I) reflections shows leguernite is monoclinic, space group P2, with a = 11.2486(11), b = 5.6568(6), c = 11.9139(10) Å, β = 99.177(7)°, V = 748.39 Å3, Z = 1. The crystal structure of leguernite consists of (001) layers with composition
Lukkulaisvaaraite*
A. Vymazalové, T.L. Grokhovskaya, F. Laufek and V.A. Rassulov (2014) Lukkulaisvaaraite, Pd14Ag2Te9, a new mineral from Lukkulaisvaara intrusion, northern Russian Karelia, Russia. Mineralogical Magazine, 78(7), 1743–1754.Vymazalové A., Grokhovskaya T.L., Laufek F., Rassulov V.A. , 2014"Lukkulaisvaaraite, Pd14Ag2Te9, a new mineral from Lukkulaisvaara intrusion, northern Russian Karelia, Russia" Mineralogical Magazine, vol. 78, no. 7, p. 1743–1754.
Lukkulaisvaaraite (IMA 2013-015), ideally Pd14Ag2Te9, is a new mineral found at the Lukkulaisvaara intrusion, northern Karelia, Russia. The mineral occurs with other platinum group element (PGE) minerals in gabbronorite from the Early Proterozoic Lukkulaisvaara layered intrusion. The mineral formed under post-magmatic conditions below 600 °C and was found rimmed by tulameenite and accompanied randomly by telargpalite and Bi-rich kotulskite, enclosed within chalcopyrite in association with millerite, bornite, hematite, moncheite, tulameenite, hongshiite, telluropalladinite, sperrylite, palarstanide, and polymineralic platinum-group mineral grains. Lukkulaisvaaraite is opaque with gray streak, a metallic luster and is brittle. The micro-indentation hardness VHN20 =355 (339–371) kg/mm2, corresponds to ~4 of a Mohs scale. In plane-polarized light, lukkulaisvaaraite is light gray with a brownish tinge, has strong bireflectance, light brownish-gray to grayish-brown pleochroism. Anisotropy is distinct to strong. No internal reflections were observed. Reflectance values were measured in air between 400 and 700 nm in 20 nm intervals. The values for COM wavelengths [Rmin, Rmax % (λ nm)] are: 40.9, 48.3 (470); 47.6, 56.4 (546); 52.1, 61.0 (589); 57.5, 65.2 (650). The average of 5 electron probe WDS analyses is [wt% (range)]: Pd 52.17 (51.06–53.27), Ag 7.03 (6.26–7.69), Te 40.36 (39.77–41.23), Bi 0.05 (0.03–0.09), total 99.61. This gives the empirical formula Pd14.05Ag1.88Te9.06 based on 25 apfu. The strongest lines in the X-ray powder-diffraction pattern of synthetic lukkulaisvaaraite [d Å (I%; hkl)] are: 2.832 (58; 130,310), 2.809 (92; 213), 2.554 (66; 312), 2.431 (41; 321,231), 2.137 (57; 411,141), 2.1015 (52; 233,323), 2.045 (100; 314), 2.003 (63; 420,240), 1.970 (30; 006), 1.405 (30; 246,426), 1.319 (36; 543,453). The crystal structure was solved and refined from the powder X-ray diffraction (XRD) data of synthetic Pd14Ag2Te9. The mineral is tetragonal, space group I4/m, with a = 8.9599(6), c = 11.822(1) Å, V = 949.1 Å3, and Z = 2. Lukkulaisvaaraite has a unique structure type and shows similarities to that of sopcheite (Ag4Pd3Te4) and palladseite (Pd17Se15). The structure can be viewed as a three-dimensional framework composed of two types of blocks of polyhedra interconnected by common Te atoms. There are four independent metal sites (M1–M4) and two Te sites where M(1) can be viewed as in transition between tetrahedral and square planar, M(2) and M(3) are at the centers of rectangles formed by Te atoms and where M(4) site is surrounded by four M(1) and four M(2) sites in a distorted square antiprismatic coordination. The mineral is named for the type locality. The holotype is deposited in the Department of Mineralogy of the National Museum, Prague, Czech Republic. O.C.G.
Minjiangite*
C. Rao, F. Hatert, R.C. Wang, X.P. Gu, F. Dal Bo and C.W. Dong (2015) Minjiangite, BaBe2(PO4)2, a new mineral from Nanping No. 31 pegmatite, Fujian Province, southeastern China. Mineralogical Magazine, 79(5), 1195–1202.Rao C., Hatert F., Wang R.C., Gu X.P., Dal Bo F., Dong C.W. , 2015"Minjiangite, BaBe2(PO4)2, a new mineral from Nanping No. 31 pegmatite, Fujian Province, southeastern China" Mineralogical Magazine, vol. 79, no. 5, p. 1195–1202.
F. Dal Bo, F. Hatert, and M. Baijot (2014) Crystal chemistry of synthetic M2+Be2P2O8 (M2+ = Ca, Sr, Pb, Ba) beryllophosphates. Canadian Mineralogist, 52(2), 337–350.Dal Bo F., Hatert F., Baijot M. , 2014"Crystal chemistry of synthetic M2+Be2P2O8 (M2+ = Ca, Sr, Pb, Ba) beryllophosphates" Canadian Mineralogist, vol. 52, no. 2, p. 337–350.
Minjiangite (IMA 2013-021), ideally BaBe2(PO4)2, is a new mineral found at in the Nanping No. 31 pegmatite, located in the southeastern margin of the Caledonian folded belt in the northwest Fujian Province, southeastern China (118°06′ E, 26°40′ N), where it occurs in the Be-rich secondary assemblages observed in the pegmatite. Rock samples of minjiangite were collected on the dumps from the mine opening at the 515 m level. Minjiangite crystals occur along fractures cutting montebrasite crystals altered during a late hydrothermal stage at which Ba and Sr were remobilized. Associated minerals mainly include quartz, muscovite, hydroxylapatite, and palermoite. Minjiangite also occurs as isolated grains included in an intimate mixture of muscovite, quartz, and hydroxylapatite. It forms subhedral to euhedral crystals, 5 to 200 μm long (usually 20 to 40 μm) and 5 to 50 μm wide. The mineral is white, transparent to translucent, with a vitreous luster. It does not exhibit fluorescence under short-wave (254 nm) and long-wave (366 nm) UV light. It is brittle with Mohs hardness ~6. No cleavage was observed. Dcalc = 3.49 g/cm3. Optical data for minjiangite were measured on synthetic minjiangite obtained by Dal Bo et al. (2014), which is uniaxial (+), with ω = 1.587(3), ε = 1.602(2) (λ = 589 nm). Raman spectra of minjiangite show (cm–1) a strong sharp peak at 1050 and a medium sharp peak 478 (stretching and bending modes of PO4) medium sharp peaks at 1233, 491 (probable Be-O vibration modes), and weak sharp peaks at 328 and 189 (Ba-O bending vibrations). FTIR of minjiangite shows bands at 1375, 1363, 1339 (BeO4 stretching), 1101, 1068, 1027 (PO4 stretching), 781 and 730 (BeO4 bending), in good agreement with data obtained by Dal Bo et al. (2014) for the synthetic material. Average of 8 electron probe WDS analyses is [wt% (range)]: P2O5 40.16 (39.51–40.78), BaO 43.01 (42.42–43.74), BeO 14.06 (by SIMS), SiO2 0.17 (0–0.41), CaO 0.17 (0.02–0.37), SrO 0.08 (0.01–0.24), FeO 0.03 (0–0.07), MgO 0.01 (0–0.02), TiO2 0.07 (0.0–0.19), K2O 0.05 (0.02–0.11), Na2O 0.11 (0.06–0.13), total 97.92. The empirical formula, calculated on the basis of 8 O apfu is: (Ba0.99Ca0.01Na0.01)∑1.01Be1.98(P1.99Si0.01)∑2.00O8. The strongest X-ray powder diffraction lines [d Å (I%; hkl)] are: 3.763 (100; 101), 2.836 (81.3; 102), 2.515 (32.3; 110), 2.178 (25.6; 200), 2.162 (19; 103), 2.090 (63.9; 201), 1.770 (16.2; 113), 1.507 (25.4; 212). Unit-cell parameters calculated from the powder data are: a = 5.030(8), c = 7.467(2) Å, V = 163.96 Å3. Refinement of X-ray diffraction data collected on a singlecrystal of the synthetic analog BaBe2(PO4)2 yielded Rall = 0.021 for 120 unique reflections. Minjiangite is hexagonal, P6/mmm, with unit-cell parameters of a = 5.029(1), c = 7.446(1)Å, V = 163.51 Å3, Z = 1. Its crystal structure is topologically similar to that of the hexagonal feldspar dmisteinbergite (CaAl2Si2O8). It is based on a double layer of tetrahedra containing both Be and P, which are assembled in six-membered rings and stacked parallel to the c axis, forming channels. Tetrahedra are linked by sharing their apexes, forming a double layer; Ba atoms are located in 12-coordinated polyhedra occurring between two double layers. Be and P are disordered among the tetrahedra of the double layer in the synthetic analog. This disordered Be-P distribution is confirmed by the broad absorption bands observed in the infrared spectrum of minjiangite. The mineral is named after the Minjiang River, located near the Nanping pegmatite. The holotype specimen is deposited at the Geological Museum of China, Beijing, China, catalogue number M11842. A cotype of natural minjiangite is deposited at the Laboratory of Mineralogy, University of Liège (catalogue number 20390), as well as the synthetic crystal used for single-crystal structure determination (catalogue number 20386). F.C.
Möhnite*
N.V. Chukanov, S.M. Aksenov, R.K. Rastsvetaeva, I.V. Pekov, D.I. Belakovskiy and S.N. Britvin (2015) Möhnite, (NH4) K2Na(SO4)2, a new guano mineral from Pabellón de Pica, Chile. Mineralogy and Petrology, 109, 643–648.Chukanov N.V., Aksenov S.M., Rastsvetaeva R.K., Pekov I.V., Belakovskiy D.I., Britvin S.N. , 2015"Möhnite, (NH4) K2Na(SO4)2, a new guano mineral from Pabellón de Pica, Chile" Mineralogy and Petrology, vol. 109, p. 643–648.
Möhnite (IMA 2014-101), ideally (NH4)K2Na(SO4)2, is a new supergene mineral found in a guano deposit on the Pabellón de Pica mountain, near Chanabaya, Iquique Province, Tarapacá Region, Chile e (20°55′ S, 70°08′ W), which is of particular interest from the viewpoint of the behavior of copper in lithospheric processes, being the type locality of several N-bearing and organic copper minerals, where chalcopyrite served as source for copper. Associated minerals are salammoniac, halite, joanneumite, natroxalate, nitratine, chanabayaite, and a clay mineral. Möhnite crystals overgrow crystalline crusts of salammoniac and encrust cavities in salammoniac aggregates and form random aggregates and clusters (up to 1 mm across), as well as crusts consisting of imperfect bipyramidal, light brown to brown spindle-shaped crystals up to 0.07×0.07×0.15 mm in size. It does not exhibit fluorescence under UV light. It is brittle with no cleavage observed and Mohs hardness is 3. Dmeas = 2.4(1) (measured by flotation in heavy liquids) and Dcalc = 2.461 g/cm3. Möhnite dissolves in water but is stable in dry air. Under plane-polarized light möhnite is light brownish-yellow and non-pleochroic. In crossed nicols it looks isotropic. The mineral is optically neutral, with ε and ω = 1.505(2) (λ = 589 nm). FTIR spectrum of möhnite shows bands at (cm-1; s = strong, m = medium; w = weak): 3240m, 3076m, 2150w, 2078w, 1431, 1165s, 1111s, 988m, 836w, 775w, 619s, 555w, 519w, 450w. Band assignment are in agreement with the presence of
References cited
Frondel, C. (1950) Notes on arcanite, ammonian aphthitalite and oxammite. American Mineralogist, 35, 596–598.Frondel C. , 1950"Notes on arcanite, ammonian aphthitalite and oxammite" American Mineralogist, vol. 35, p. 596–598.
Moraskoite*
Ł. Karwowski, J. Kusz, A. Muszynski, R. Kryza, M. Sitarz and E.V. Galuskin (2015) Moraskoite, Na2Mg(PO4)F, a new mineral from the Morasko IAB-MG iron meteorite (Poland). Mineralogical Magazine, 79(2), 387–398Karwowski Ł., Kusz J., Muszynski A., Kryza R., Sitarz M., Galuskin E.V. , 2015"Moraskoite, Na2Mg(PO4)F, a new mineral from the Morasko IAB-MG iron meteorite (Poland)" Mineralogical Magazine, vol. 79, no. 2, p. 387–398.
Moraskoite (IMA 2013-084), ideally Na2Mg(PO4)F, is a new mineral found in the Morasko IAB-MG iron meteorite. Moraskoite occurs in a graphite-troilite inclusion that is rimmed by a schreibersite-cohenite halo, enclosed in a kamacite-taenite matrix, and is interpreted as being a primary phosphate. Associated minerals include chlorapatite, buchwaldite, brianite, merrillite, a new phosphate phase of composition Na4MgCa3(PO4)4, chromite, enstatite (bronzite), kosmochlor, kosmochlor-augite, olivine, albite, orthoclase, quartz, cohenite, schreibersite, nickelphosphide, altaite, pyrrhotite, sphalerite, daubreelite, djerfischerite, whitlockite, and native Cu. Moraskoite forms aggregates up to 1.5 mm, with individual grains of irregular shape 20–300 μm across, and also occurs in smaller single grains intergrown with buchwaldite and filled with numerous graphite inclusions. Moraskoite is colorless and transparent with a white streak and vitreous luster. It has irregular, conchoidal fracture, and rarely observed cleavage. The density was not measured because of the small grain size and intimate intergrowth with graphite; Dcalc = 2.925 g/cm3. Mohs hardness is 4–5. The wedge-shaped form of the grains did not allow the exact determination of optical constants. The mineral is non-pleochroic, optically biaxial, with very low birefringence (~0.004) and small 2V angle. The refractive index measured in a random cross-section is 1.550(4) (λ = 589 nm). Fluorescence is weak blue in UV radiation (254 and 360 nm). The Raman spectrum shows bands (cm–1) at 1114 (ν3 antisymmetric stretching vibrations of
Nickelpicromerite*
E.V. Belogub, S.V. Krivovichev, I.V. Pekov, A.M. Kuznetsov, V.O. Yapaskurt, V.A. Kotlyarov, N.V. Chukanov and D.I. Belakovskiy (2015) Nickelpicromerite, K2Ni(SO4)2·6H2O, a new picromerite-group mineral from Slyudorudnik, South Urals, Russia. Mineralogy and Petrology, 109, 143–152.Belogub E.V., Krivovichev S.V., Pekov I.V., Kuznetsov A.M., Yapaskurt V.O., Kotlyarov V.A., Chukanov N.V., Belakovskiy D.I. , 2015"Nickelpicromerite, K2Ni(SO4)2·6H2O, a new picromerite-group mineral from Slyudorudnik, South Urals, Russia" Mineralogy and Petrology, vol. 109, p. 143–152.
Nickelpicromerite (IMA 2012-053), ideally K2Ni(SO4)·6H2O, is a new supergene mineral found at the vein #169 of the Ufaley quartz deposit, near the town of Slyudorudnik, Kyshtym District, Chelyabinsk area, South Urals, Russia (55°40′12′N 60°21′17″E). It occurs with gypsum and goethite in fractures of slightly weathered actinolite-talc schist containing partially altered (vermiculitized) biotite, sulfides (pyrrhotite, pentlandite, millerite, pyrite, and marcasite) and, rarely, unaltered chromite. Nickelpicromerite occurs as equant to short prismatic or tabular crystals up to 0.07 mm and anhedral grains up to 0.5 mm (typically <0.1 mm). The mineral is transparent, light greenish blue (light turquoise-colored), with white streak and vitreous luster. It does not fluoresce either in UV or in cathode rays. It is brittle with stepped fracture and Mohs hardness ~2–2½. Dmeas = 2.20(2) g/cm3 (by flotation in CHBr3+CH3OH); Dcalc = 2.222 g/cm3. Nickelpicromerite is optically biaxial (+), with α = 1.486(2), β = 1.489(2), γ = 1.494(2) (λ = 589 nm); 2Vmeas = 75(10)°, 2Vcalc = 76°. FTIR spectra of nickelpicromerite and picromerite are very similar. Bands that could be assigned to
Pilawite-(Ce)*
A. Pieczka, F.C. Hawthorne, M.A. Cooper, E. Szełęg, A. Szuszkiewicz, K. Turniak, K. Nejbert and S. Ilnicki (2015) Pilawite-(Y), Ca2(Y, Yb)2[Al4(SiO4)4O2(OH)2], a new mineral from the Pilawa Górna granitic pegmatite, southwestern Poland: mineralogical data, crystal structure and association. Mineralogical Magazine, 79(5), 1143–1157.Pieczka A., Hawthorne F.C., Cooper M.A., Szełęg E., Szuszkiewicz A., Turniak K., Nejbert K., Ilnicki S. , 2015"Pilawite-(Y), Ca2(Y, Yb)2[Al4(SiO4)4O2(OH)2], a new mineral from the Pilawa Górna granitic pegmatite, southwestern Poland: mineralogical data, crystal structure and association" Mineralogical Magazine, vol. 79, no. 5, p. 1143–1157.
Pilawite-(Ce) (IMA 2013-125), with formula Ca2(Y, Yb)2[Al4(SiO4)4O2(OH)2], is a new mineral from a granitic pegmatite at Pilawa Górna in Lower Silesia, Poland (50°42′11.77″N 16°44′12.36″E). It occurs together with keiviite-(Y), gadolinite-(Y), hingganite-(Y), and hellandite-(Y), as inclusions in accessory allanite-(Y) within the blocky feldspar zone of a weakly zoned and weakly fractionated NYF affiliated dike, part of cogenetic pegmatites known as the Julianna pegmatitic system. The accessory minerals of the feldspar zone are black tourmaline, abundant zircon, monazite-(Ce), xenotime-(Y), single aggregates of allanitegroup minerals and occasional Nb-Ta oxides (ixiolite with inclusions of cassiterite, fersmite, rutile, and ilmenorutile). Pilawite-(Y) occurs as an aggregate ~2 mm across, of 2–3 crystals reaching 1.5 mm long, enclosed in quartz and partly overgrown by allanite-(Y). Pilawite-(Ce) has white color and streak and a vitreous luster. Crystals are brittle and Mohs hardness is 5. Parting or cleavage are not observed. Dcalc = 4.007 g/cm3. Pilawite-(Y) is non-pleochroic, optically biaxial (+), with α = 1.743(5), β = 1.754(5), γ = 1.779(5) (light not reported); 2Vmeas = 65(2)°, 2Vcalc = 68°, orientation X Λ a = 87.5° (β acute), Y // b and Z Λ a = 3.1° (β obtuse). FTIR spectrum of pilawite-(Ce) shows broad prominent band at ~2975 cm–1, a sharp band at ~2300 cm–1 and a rather ragged weaker doublet centered at ~2050 cm–1, which can be related to O-H stretching modes. The Raman spectrum shows prominent Si-O stretching bands in the range ~850–950 cm–1 and a large number of Al–O modes and lattice modes below ~600 cm–1. Average of 33 electron probe WDS spot analyses is [wt% (range)]: P2O5 0.04 (0–0.30), SiO2 28.34 (28.16–28.68), TiO2 0.26 (0–0.82), Al2O3 23.36 (22.61–23.87), Fe2O3 0.72 (0–1.18), Y2O3 22.17 (21.01–23.209, Gd2O3 0.50 (0.18–0.80), Tb2O3 0.21 (0.09–0.33), Dy2O3 2.13 (1.35–2.83), Ho2O3 0.54 (0.31–0.78), Er2O3 2.04 (1.60–2.44), Tm2O3 0.34 (0.17–0.47), Yb2O3 2.53 (1.38–3.75), Lu2O3 0.47 (0.30–0.75), FeO 0.32 (0–1.06), MnO 0.75 (0.59–1.34), CaO 12.50 (11.66–13.37), PbO 0.18 (0.12–0.28), H2O (by stoichiometry and Fe3+/Fe2+ adjusted to maintain 12 cations pfu) 2.14 (2.11–2.16), total 99.55. The empirical formula, calculated on the basis of 20 O pfu is: (Ca1.88
Ralphcannonite*
L. Bindi, C. Biagioni, T. Raber, P. Roth and F. Nestola (2015) Ralphcannonite, AgZn2TlAs2S6, a new mineral of the routhierite isotypic series from Lengenbach, Binn Valley, Switzerland. Mineralogical Magazine, 79(5), 1089–1098.Bindi L., Biagioni C., Raber T., Roth P., Nestola F. , 2015"Ralphcannonite, AgZn2TlAs2S6, a new mineral of the routhierite isotypic series from Lengenbach, Binn Valley, Switzerland" Mineralogical Magazine, vol. 79, no. 5, p. 1089–1098.
The new member of the routhierite isotypic series, ralphcannonite (IMA 2014077), ideally AgZn2TlAs2S6, was discovered in the specimen from massif sulfosalts accumulations in dolostone of the Lengenbach quarry, Binn Valley, Wallis, Switzerland. This well-known deposit is the type locality for 15 other thallium sulfosalts. Ralphcannonite is associated with dufrénoysite, hatchite, realgar, and barite. It forms black metallic euhedral equant crystals up to 50 μm with the prism {110} and pinacoid {001} as the dominant forms and bipyramids {101} and {111}, and prism {100} as an accessory forms. The mineral has black streak and is brittle with an irregular fracture. The micro-indentation hardness VHN30 = 120 (116–128) kg/mm2 corresponds to ~2–2½ of Mohs scale. The density was not measured; Dcalc = 4.927 g/cm3. In plane-polarized incident light, ralphcannonite is grayish. Under crossed polars, it is very weakly anisotropic, with grayish to light blue rotation tints. Internal reflections are very weak. No optical evidence of growth zonation was observed. The reflectance values for COM wavelengths in air are: [Rmin, Rmax% (λ nm)]: 25.8, 27.1(471.1); 25.2, 26.6 (548.3); 24.6, 25.8 (586.6); 23.9, 24.8 (652.3). The average of electron probe WDS analyses (number not given) is [wt% (range)]: Cu 2.01 (1.78–2.22), Ag 8.50 (8.19–8.80), Zn 10.94 (10.25–11.33), Fe 3.25 (3.10–3.34), Hg 7.92 (7.10–8.50), Tl 24.58 (23.87–25.26), As 18.36 (17.58–18.96), Sb 0.17 (0.09–0.25), S 24.03 (23.61–24.66), total 99.76. Other elements with Z > 9 were not detected. The empirical formula based on 12 atoms pfu is (Ag0.63Cu0.25Zn1.35)Fe0.47Hg0.32Tl0.97(As1.97Sb0.01)∑1.98S6.03. Due to the very small size and amount of crystals available, a powder X-ray diffraction pattern was not collected. The strongest lines of the calculated X-ray powder diffraction pattern [dcalc Å (Icalc%; hkl)] are: 4.100 (85; 211), 3.471 (40; 103), 2.954 (100; 222), 2.656 (20; 321), 2.465 (400), 2.460 (39; 303). The crystal structure has been solved on the basis of the X-ray single-crystal data and refined to R1 = 0.030 for 140 observed [Fo > 4σ(Fo)] reflections. The mineral is tetragonal, I
Yeomanite*
R.W. Turner, O.I. Siidra, M.S. Rumsey, Y.S. Polekhovsky, Y.L. Kretser, S.V. Krivovichev, J. Spratt and C.J. Stanley (2015) Yeomanite, Pb2O(OH)Cl, a new chain-structured Pb oxychloride from Merehead Quarry, Somerset, England. Mineralogical Magazine, 79(5), 1203–1211.Turner R.W., Siidra O.I., Rumsey M.S., Polekhovsky Y.S., Kretser Y.L., Krivovichev S.V., Spratt J., Stanley C.J. , 2015"Yeomanite, Pb2O(OH)Cl, a new chain-structured Pb oxychloride from Merehead Quarry, Somerset, England" Mineralogical Magazine, vol. 79, no. 5, p. 1203–1211.
Yeomanite (IMA 2013-024), ideally Pb2O(OH)Cl, is a new mineral found in the Mn pod mineral assemblage at Merehead (Torr Works) Quarry, near Cranmore, Somerset, England. The new mineral is named after Angela Yeoman (b. 1931) and her company, Foster Yeoman, which had been operated at the Quarry until 2006. The new mineral was found in cavities in manganese oxide pods (a mixture of manganite and pyrolusite, associated with goethite, and gangue minerals such as aragonite, calcite, and barite) that have thin rims of calcite lining the outermost edges. These cavities are filled by either mendipite, Pb3Cl2O2, or by asbestos-like fibrous aggregates of yeomanite. Other oxychloride minerals found in those pods include chloroxiphite, diaboleite, mereheadite, paralaurionite, parkinsonite, symesite, rickturnerite, and rumseyite. Mimetite, wulfenite, cerussite, “hydrocerussite,” malachite, and “crednerite” occur in the same environment. Yeomanite fibers (up to 15 mm, generally <8 mm long) form loose mats and strands, and individual fibers are. Yeomanite is white, occasionally pale gray, transparent, with a white streak and a vitreous luster. It does not fluoresce in UV radiation. The mineral is brittle. The micro-indentation hardness VHN20 = 54.5 kg/mm2 corresponding to ~2 of the Mohs scale. The perfect cleavage is parallel to fibers elongation. Density was not measured due to the fibrous nature; Dcalc = 7.303 g/cm3. In reflected light, yeomanite is light gray to gray with white internal reflections, non-pleochroic and does not have bireflectance. The reflectance values in air [Rmin, Rmax (nm)] are: 16.0, 20.2 (400), 15.4, 19.5 (420), 15.0, 18.9 (440), 14.7, 18.6 (460), 14.5, 18.4 (470), 14.4, 18.2 (480), 14.1, 17.8 (500), 13.9, 17.5 (520), 13.7, 17.3 (540), 13.7, 17.2 (546), 13.5, 17.1 (560), 13.3, 16.9 (580), 13.3, 16.8 (589), 13.2, 16.8 (600), 13.1, 16.7 (620), 13.0, 16.6 (640), 12.9, 16.6 (650), 12.8, 16.6 (660), 12.8, 16.5 (680), 12.8, 16.4 (700). The anisotropism ΔR589 = 3.58%. The average of 20 electron probe EDS analyses on three crystals of yeomanite is [(wt%, (range)]: PbO 92.3 (91.97–92.50), Cl 7.4 (7.35–7.48), H2O 1.9 (by structure data), O=Cl 1.7, total 99.9. The formula calculated on the basis of 3 O+OH+Cl pfu is: Pb1.99O0.98 (OH)1.01Cl1.01. The strongest lines of the X-ray powder diffraction pattern [d Å (I%; hkl)] are: 2.880 (100; 113), 2.802 (78; 006), 3.293 (61; 200), 3.770 (32; 011), 2.166 (22; 206), 1.662 (19; 119), 2.050 (18; 303), 3.054 (17; 105). The crystal structure of yeomanite was solved by direct methods and refined to R1 = 10.6%. The mineral is orthorhombic, Pnma, a = 6.585(10), b = 3.855(6), c = 17.26(1) Å, V = 438 Å3, and Z = 4. Crystal structure of yeomanite is based on [O(OH)Pb2]+ chains that are formed by oxycentered OPb4 tetrahedra joined by OHPb3 triangles. The holotype specimen is housed in the Natural History Museum, London, England, and a cotype specimen is stored in the Smithsonian Institution in Washington, D.C., U.S.A. Yu.U.
* All minerals marked with an asterisk have been approved by the IMA CNMMC.
† For a complete listing of all IMA-validated unnamed minerals and their codes, see http://pubsites.uws.edu.au/ima-cnmnc/.
© 2016 by Walter de Gruyter Berlin/Boston