New Mineral Names*

Total Page:16

File Type:pdf, Size:1020Kb

New Mineral Names* American Mineralogist, Volume 95, pages 1357–1361, 2010 New Mineral Names* PAULA C. PIILONEN † AND GLENN POIRIER Mineral Sciences Division, Canadian Museum of Nature, P.O. Box 3443, Station D, Ottawa, Ontario K1P 6P4, Canada NEW MINERALS lines on the pattern [dobs in Å(Iobs%, hkl)] include: 3.712(13,111), 3.476(11,3.473), 3.075(25,201), 2.859(100,211), 2.4563(32,310), ALU M OÅKER M ANITE * 1.9413(11,400), 1.8303(13,330), 1.7634(11,411), 1.7569(19,312), D. Wiedenmann, A.N. Zaitsev, S.N. Britvin, S.V. Krivovichev, 1.7364(13,420), and 1.3859(13,521). The crystal structure of 2+ alumoåkermanite was solved and refined using a 0.22 × 0.14 × and J. Keller (2009) Alumoåkermanite, (Ca,Na)2(Al,Mg,Fe ) 0.12 mm crystal mounted on a Stoe IPDS II Image-Plate-based (Si2O7), a new mineral from the active carbonatite-nephelin- ite-phonolite volcano Oldoinyo Lengai, northern Tanzania. X-ray diffractometer. The structure was refined using starting Mineral. Mag., 73, 373–384. parameters from a synthetic sodic melilite (Louisnathan 1970, Z. Kristallogr., 23, 314–321) inverted to obtain the absolute correct Alumoåkermanite is a new member of the melilite group structure model. The data were refined to R1 = 0.018 based on from the Oldoinyo Lengai volcano, northern Tanzania. The 439 unique reflections with |Fo| ≥ 4σF. The mineral is tetrago- 3 new mineral was found in several samples from the volcano nal, P421m, a = 7.7620(7), c = 5.0311(5) Å, V = 303.12(5) Å , and surrounding area. It occurs in evolved, olivine-free melilite- Z = 2. The structural formula can thus be written as (Ca1.5Na0.5) nephelinitic ashes and lapilli-tuffs from the 1966/67 and pre-1966 (Al0.5Fe0.3Mg0.2)(Si2O7), which agrees with the WDS data. The eruptions along with nepheline, aegirine-augite, and microcrysts structure of alumoåkermanite is identical in topology to other of matrix-minerals including nepheline, aegirine-augite, combe- melilite-group minerals with [(Al,Mg)Si2O7)] sheets interwoven ite, spinel-group minerals, wollastonite, melanite, titanite, and with layers of (Ca,Na) cations. The absence of Al in the silicate sodalite. Alumoåkermanite occurs as tabular phenocrysts up 1.5 tetrahedra site is unique in alumoåkermanite. mm, and as microphenocrysts in the fine-grained groundmass. It The name is for its composition and relationship to other is transparent, light brown, has a white streak, a Mohs hardness members of the melilite group. The mineral and name have been of ~4.5–5, is brittle with an uneven fracture, and no discernible approved by the IMA CNMNC (IMA no. 2008-049). Co-type fracture or cleavage. It does not fluoresce in either short-wave specimens have been deposited in the Mineralogical Museum, 3 Department of Mineralogy, St. Petersburg State University, St. or long-wave UV light. It has a Dmeas = 2.96(2) g/cm and Dcalc = 3.00 g/cm3. Alumoåkermanite is uniaxial negative (–), with Petersburg, Russia (OL218, catalog no. 1/19407), and the Fers- ω = 1.635(1) for both samples, and ε = 1.626(1) (OL244) and man Mineralogical Museum, Russian Academy of Sciences, 1.624(2) (OL218). Under cross-polarized light, alumoåkermanite Moscow, Russia (OL244, catalog no. 3823/1). P.C.P. has a yellow to orange-red interference color, straight extinction, CÁ M ARAITE * positive elongation, and is non-pleochroic. The average chemical composition (WDS) of eight analyses E. Sokolova, Y. Abdu, F.C. Hawthorne, A.V. Stepanov, G.K. Bekenova, and P.E. Kotel’Nikov (2009) Cámaraite, Ba3NaTi4 gave SiO2 43.73, TiO2 0.09, Al2O3 8.32, Fe2O3 2.14, FeO 4.55, 2+ (Fe ,Mn)8(Si2O7)4O4(OH,F)7. I. A new Ti-silicate mineral MnO 0.22, MgO 4.36, CaO 30.24, SrO 0.91, Na2O 5.70, K2O from the Verkhnee Espe Deposit, Akjailyautas Mountains, 0.10, sum 100.23 wt%, corresponding to (Ca1.48Na0.50Sr0.02K0.01)Σ2.01 2+ 3+ Kazakhstan. Mineral. Mag., 73, 847–854. (Al0.44Mg0.30Fe 0.17Fe 0.07Mn0.01)Σ0.99(Si1.99Al0.01O7) based on seven 2+ oxygen atoms, and an ideal formula of (Ca,Na)2(Al,Mg,Fe ) F. Cámara, E. Sokolova, and F. Nieto (2009) Cámaraite, Ba3Na (Si2O7). 2+ Powder X-ray diffraction data were collected on a Stoe Stadi Ti4(Fe ,Mn)8(Si2O7)4O4(OH,F)7. II. The crystal structure and P diffractometer (CuKα radiation) in transmission geometry. Re- crystal chemistry of a new group-II Ti-disilicate mineral. fined unit-cell parameters for the powder X-ray diffraction data Mineral. Mag., 73, 855–870. are a = 7.7661(4), c = 5.0297(4) Å, V = 303.4(1) Å3. The strongest Cámaraite is a new mineral from the Verkhnee Espe rare- element deposit located at the northern exo-contact of the large *All minerals marked with an asterisk have been approved by Akjailyautas granite massif, northern Tarbagatai mountain range, the IMA CNMMC. eastern Kazakhstan. It was found within a part of the deposit † E-mail: [email protected] where alkali-rich fenites have been extensively recrystallized. 0003-004X/10/0809–1357$05.00/DOI: 10.2138/am.2010.565 1357 1358 NEW MINERAL NAMES Cámaraite is a hydrothermal mineral and occurs along with mineralogy and crystallography, particularly with respect to Ti- bafertisite, jinshajiangite, zircon, pyrochlore-group minerals, silicates, amphiboles, arrojadite-group minerals and cancrinite- thorite, monazite, and xenotime at the exo-contact of the fen- group minerals. The mineral and name have been approved by itized and granitized host rock. The mineral occurs on fracture IMA CNMNC (IMA no. 2009-11). Holotype material has been surfaces, intergrown with jinshajiangite and bafertisite (8 × 15 deposited at the Fersman Mineralogical Museum, Moscow, × 2 mm intergrowths), and as star-shaped aggregates of crystals. Russia (catalog no. 3828/1 and 3828/2). P.C.P. Cámaraite is orange-red to brownish-red, platy on {001}, has a pale-yellow streak, a vitreous luster, is brittle with a {001} DALIRANITE * cleavage, no observed parting, a Mohs hardness of <5, and does W.H. Paar, A. Pring, Y. Moëlo, C.J. Stanley, H. Putz, D. Topa, not fluoresce under cathode or UV light. The mineral has Dmeas A.C. Roberts, and R.S.W. Braithwaite (2009) Daliranite, 3 = 3.871(1) and Dcalc = 4.018 g/cm . Cámaraite is biaxial positive PbHgAs2S6, a new sulfosalt from the Zarshouran Au-As (+), 2Vmeas = 93(1)°, with refractive indices > 1.80 (rcalc = 1.866). deposit, Takab region, Iran. Mineral. Mag., 73, 871–881. It is strongly pleochroic, X = light brown, Y = reddish brown, Z = yellow-brown, Z < X < Y. Daliranite is a new sulfosalt mineral from the Zarshouran Au- The chemical composition of cámaraite was determined As deposit, 42 km north of the town of Takab, West Azarbaijan by WDS methods with the average (range) of 13 analyses Province, northwest Iran. The mineral has been known from this giving Nb2O5 1.57(1.36–1.82), SiO2 25.25(25.09–25.40), locality since the 1970s, often mislabeled as ludlockite, which it TiO2 15.69(15.41–15.88), ZrO2 0.33(0.22–0.52), Al2O3 resembles. Daliranite occurs growing on orpiment and quartz, 0.13(0.09–0.22), Fe2O3 = 2.77, FeOtot 16.54(18.76–19.37), MnO or, rarely, as matted nests along cracks and fractures. The matted 9.46(9.34–9.60), ZnO 0.12(0.09–0.17), MgO 0.21(0.20–0.22), nests consist of acicular, flexible hair-like fibers <200 μm long CaO 0.56(0.48–0.70), BaO 21.11(20.60–21.66), Na2O 1.41(1.32– and <3μm in diameter elongated parallel to [010]. The mineral 1.48), K2O 0.84(0.80–0.89), H2Ocalc 1.84, F 3.11(2.93–3.33), is vibrant orange-red, has a pale orange-red streak, is transpar- O≡F –1.31, sum 99.63 wt%, corresponding to the empirical ent with an adamantine luster, and has a Mohs hardness of >2. formula based on 39 anions of (Ba2.61K0.34)Σ2.95(Na0.86Ca0.14)Σ1 Neither cleavage nor fracture was observed, nor is it fluorescent. 2+ 3+ (Ti3.72Nb0.22Al0.05)Σ3.99(Fe 4.36Fe 0.66Mn2.53Mg0.10Zr0.05Zn0.03Ca0.05)Σ7.78 Optically, daliranite has a gray color with a distinctly higher re- 2+ Si7.97O35.89H3.88F3.11, ideally Ba3NaTi4(Fe ,Mn)8(Si2O7)4O4 flectance than that of orpiment and abundant orange-red internal 57 (OH,F)7. Mössbauer spectroscopy (RT, Co source) allowed reflections. Reflectance data were determined in air (%/nm): 3+ for the determination of the Fe /Fetot ratio [0.13(8)] and the 32.9/470, 30.5/546, 34.0/589, and 39.5/650. confirmation that all Fe is octahedrally coordinated. Chemical analyses of daliranite (EMPA) gave an average Powder X-ray diffraction data were collected on a 57.3 mm composition (eight analyses) of Pb 23.26, Hg 24.77, Tl 0.19, As Debye-Scherrer camera (CoKα radiation). Refined unit-cell 18.75, S 22.48, sum 89.44%, resulting in an empirical formula parameters are a = 10.678(4), b = 13.744(8), c = 21.40(2) Å, based on 10 apfu (and after normalizing the EMPA data) of 3 α = 99.28(8), β = 92.38(5), γ = 90.00(6)°, V = 3096(3) Å . The Pb0.95Tl0.01Hg1.04As2.10S5.91, with an ideal formula of PbHgAs2S6, strongest lines in the diffraction pattern [dobs in Å(Iobs%, hkl)] which requires Pb 27.63, Hg 26.75, As 19.98, S 25.65, sum are: 3.83(30,204), 3.39(50,224), 3.26(20,043), 3.18(50,2 25), 100.00 wt%.
Recommended publications
  • L. Jahnsite, Segelerite, and Robertsite, Three New Transition Metal Phosphate Species Ll. Redefinition of Overite, an Lsotype Of
    American Mineralogist, Volume 59, pages 48-59, 1974 l. Jahnsite,Segelerite, and Robertsite,Three New TransitionMetal PhosphateSpecies ll. Redefinitionof Overite,an lsotypeof Segelerite Pnur BnnN Moone Thc Departmcntof the GeophysicalSciences, The Uniuersityof Chicago, Chicago,Illinois 60637 ilt. lsotypyof Robertsite,Mitridatite, and Arseniosiderite Peur BmaN Moonp With Two Chemical Analvsesbv JUN Iro Deryrtrnent of GeologicalSciences, Haraard Uniuersity, Cambridge, Massrchusetts 02 I 38 Abstract Three new species,-jahnsite, segelerite, and robertsite,-occur in moderate abundance as late stage products in corroded triphylite-heterosite-ferrisicklerite-rockbridgeite masses, associated with leucophosphite,hureaulite, collinsite, laueite, etc.Type specimensare from the Tip Top pegmatite, near Custer, South Dakota. Jahnsite, caMn2+Mgr(Hro)aFe3+z(oH)rlPC)oln,a 14.94(2),b 7.14(l), c 9.93(1)A, p 110.16(8)", P2/a, Z : 2, specific gavity 2.71, biaxial (-), 2V large, e 1.640,p 1.658,t l.6lo, occurs abundantly as striated short to long prismatic crystals, nut brown, yellow, yellow-orange to greenish-yellowin color.Formsarec{001},a{100},il2oll, jl2}ll,ft[iol],/tolll,nt110],andz{itt}. Segeierite,CaMg(HrO)rFes+(OH)[POdz, a 14.826{5),b 18.751(4),c7.30(1)A, Pcca, Z : 8, specific gaavity2.67, biaxial (-), 2Ylarge,a 1.618,p 1.6t5, z 1.650,occurs sparingly as striated yellow'green prismaticcrystals, with c[00], r{010}, nlll0l and qll2l } with perfect {010} cleavage'It is the Feg+-analogueofoverite; a restudy on type overite revealsthe spacegroup Pcca and the ideal formula CaMg(HrO)dl(OH)[POr]r. Robertsite,carMna+r(oH)o(Hro){Ponlr, a 17.36,b lg.53,c 11.30A,p 96.0o,A2/a, Z: 8, specific gravity3.l,T,cleavage[l00] good,biaxial(-) a1.775,8 *t - 1.82,2V-8o,pleochroismextreme (Y, Z = deep reddish brown; 17 : pale reddish-pink), @curs as fibrous massesand small wedge- shapedcrystals showing c[001 f , a{1@}, qt031}.
    [Show full text]
  • Mineral Processing
    Mineral Processing Foundations of theory and practice of minerallurgy 1st English edition JAN DRZYMALA, C. Eng., Ph.D., D.Sc. Member of the Polish Mineral Processing Society Wroclaw University of Technology 2007 Translation: J. Drzymala, A. Swatek Reviewer: A. Luszczkiewicz Published as supplied by the author ©Copyright by Jan Drzymala, Wroclaw 2007 Computer typesetting: Danuta Szyszka Cover design: Danuta Szyszka Cover photo: Sebastian Bożek Oficyna Wydawnicza Politechniki Wrocławskiej Wybrzeze Wyspianskiego 27 50-370 Wroclaw Any part of this publication can be used in any form by any means provided that the usage is acknowledged by the citation: Drzymala, J., Mineral Processing, Foundations of theory and practice of minerallurgy, Oficyna Wydawnicza PWr., 2007, www.ig.pwr.wroc.pl/minproc ISBN 978-83-7493-362-9 Contents Introduction ....................................................................................................................9 Part I Introduction to mineral processing .....................................................................13 1. From the Big Bang to mineral processing................................................................14 1.1. The formation of matter ...................................................................................14 1.2. Elementary particles.........................................................................................16 1.3. Molecules .........................................................................................................18 1.4. Solids................................................................................................................19
    [Show full text]
  • New Mineral Names*,†
    American Mineralogist, Volume 106, pages 1360–1364, 2021 New Mineral Names*,† Dmitriy I. Belakovskiy1, and Yulia Uvarova2 1Fersman Mineralogical Museum, Russian Academy of Sciences, Leninskiy Prospekt 18 korp. 2, Moscow 119071, Russia 2CSIRO Mineral Resources, ARRC, 26 Dick Perry Avenue, Kensington, Western Australia 6151, Australia In this issue This New Mineral Names has entries for 11 new species, including 7 minerals of jahnsite group: jahnsite- (NaMnMg), jahnsite-(NaMnMn), jahnsite-(CaMnZn), jahnsite-(MnMnFe), jahnsite-(MnMnMg), jahnsite- (MnMnZn), and whiteite-(MnMnMg); lasnierite, manganflurlite (with a new data for flurlite), tewite, and wumuite. Lasnierite* the LA-ICP-MS analysis, but their concentrations were below detec- B. Rondeau, B. Devouard, D. Jacob, P. Roussel, N. Stephant, C. Boulet, tion limits. The empirical formula is (Ca0.59Sr0.37)Ʃ0.96(Mg1.42Fe0.54)Ʃ1.96 V. Mollé, M. Corre, E. Fritsch, C. Ferraris, and G.C. Parodi (2019) Al0.87(P2.99Si0.01)Ʃ3.00(O11.41F0.59)Ʃ12 based on 12 (O+F) pfu. The strongest lines of the calculated powder X-ray diffraction pattern are [dcalc Å (I%calc; Lasnierite, (Ca,Sr)(Mg,Fe)2Al(PO4)3, a new phosphate accompany- ing lazulite from Mt. Ibity, Madagascar: an example of structural hkl)]: 4.421 (83; 040), 3.802 (63, 131), 3.706 (100; 022), 3.305 (99; 141), characterization from dynamic refinement of precession electron 2.890 (90; 211), 2.781 (69; 221), 2.772 (67; 061), 2.601 (97; 023). It diffraction data on submicrometer sample. European Journal of was not possible to perform powder nor single-crystal X-ray diffraction Mineralogy, 31(2), 379–388.
    [Show full text]
  • New Mineral Names*
    American Mineralogist, Volume 96, pages 1654–1661, 2011 New Mineral Names* PAULA C. PIILONEN,1,† RALPH ROWE,1 GLENN POIRIER,1 AND KIMBERLY T. TAIT2 1Mineral Sciences Division, Canadian Museum of Nature, P.O. Box 3443, Station D, Ottawa, Ontario K1P 6P4, Canada 2Department of Natural History, Royal Ontario Museum,100 Queen’s Park, Toronto, Ontario M5S 2C6, Canada NEW MINERALS The streak is white and the Mohs hardness is estimated to be about 1½. Thin crystal fragments are flexible, but not elastic. The fracture is irregular and there are three cleavage directions: {001} AFMITE* perfect, {010} and {110} good. The mineral is non-fluorescent A.R. Kampf, S.J. Mills, G.R Rossman, I.M. Steele, J.J. Pluth, under all wavelengths of ultraviolet radiation. The density mea- sured by sink-float in aqueous solution of sodium polytungstate and G. Favreau (2011) Afmite, Al3(OH)4(H2O)3(PO4) is 2.39(3) g/cm3. The calculated density, based on the empirical (PO3OH)·H2O, a new mineral from Fumade, Tarn, France: de- 3 scription and crystal structure. Eur. J. Mineral., 23, 269–277. formula and single-crystal cell, is 2.391 g/cm and that for the ideal formula is 2.394 g/cm3. Afmite is found at Fumade, Castelnau-de-Brassac, Tarn, Electron microprobe analyses provided Al2O3 40.20 and France (43°39′30″N, 2°29′58″E). The phosphates occur in P2O5 38.84 wt% and CHN analyses provided H2O 25.64 wt%, fractures and solution cavities in shale/siltstone exposed in total 103.68 wt%.
    [Show full text]
  • 259 XLL-Chemical Researches on Some New and Rare Corn.Ish
    259 XLL-Chemical Researches on some new and rare Corn.ish Miwrals. By A. H. CHURCH,M.A., Professor of Chemistry, Royal Agricultural College, Cirencester. I. Hydrated Cerous Phosphate. THEhydrous phosphate which forms the subject of the present commnnication, occurs as a thin crust closely investing a quartzose matrix. This crust is made up of very minute crystals, generally occurring in fan-like aggregations of single rows of prisms. The faces of union of these groups are parallel to the larger lateral prismatic planes. Occasionally the structure is almost columnar, or in radiating groups, presenting a drusy surface and a general appearance somewhat resemlding that of mavellite. The mode of attachment of the crystals is such that only one of the end-faces of the prisms can be studied fully. It would appear that the crystals belong to the oblique system, and are prismatically deve- loped forms. The end-face, 001, presents the aspect of an unmodi- fied rhomboid ; occasionally, however, its diagonally opposite acute angles are replaced. Whether the appearances then presented by the crystal are due to a truncation of the solid acute angle, OF to a bevelling of the acute prismatic edge, it is difficult to say, owing to the microscopic siee of the crystals, and their parallel mode of aggregation. The plane of cleavage most easily obtained is parallel to the end- face 001; this cleavage is very perfect. Other cleavages are obtainable; one parallel to the plane previously referred to as replaciug the acute solid angles or acute prismatic edges of the crystal, the other parallel to the larger lateral prismatic planes.
    [Show full text]
  • Journal of the Russell Society, Vol 4 No 2
    JOURNAL OF THE RUSSELL SOCIETY The journal of British Isles topographical mineralogy EDITOR: George Ryba.:k. 42 Bell Road. Sitlingbourn.:. Kent ME 10 4EB. L.K. JOURNAL MANAGER: Rex Cook. '13 Halifax Road . Nelson, Lancashire BB9 OEQ , U.K. EDITORrAL BOARD: F.B. Atkins. Oxford, U. K. R.J. King, Tewkesbury. U.K. R.E. Bevins. Cardiff, U. K. A. Livingstone, Edinburgh, U.K. R.S.W. Brai thwaite. Manchester. U.K. I.R. Plimer, Parkvill.:. Australia T.F. Bridges. Ovington. U.K. R.E. Starkey, Brom,grove, U.K S.c. Chamberlain. Syracuse. U. S.A. R.F. Symes. London, U.K. N.J. Forley. Keyworth. U.K. P.A. Williams. Kingswood. Australia R.A. Howie. Matlock. U.K. B. Young. Newcastle, U.K. Aims and Scope: The lournal publishes articles and reviews by both amateur and profe,sional mineralogists dealing with all a,pecI, of mineralogy. Contributions concerning the topographical mineralogy of the British Isles arc particularly welcome. Not~s for contributors can be found at the back of the Journal. Subscription rates: The Journal is free to members of the Russell Society. Subsc ription rates for two issues tiS. Enquiries should be made to the Journal Manager at the above address. Back copies of the Journal may also be ordered through the Journal Ma nager. Advertising: Details of advertising rates may be obtained from the Journal Manager. Published by The Russell Society. Registered charity No. 803308. Copyright The Russell Society 1993 . ISSN 0263 7839 FRONT COVER: Strontianite, Strontian mines, Highland Region, Scotland. 100 mm x 55 mm.
    [Show full text]
  • THE CRYSTAL STRUCTURE of Pb8o5(OH)2Cl4, a SYNTHETIC ANALOGUE of BLIXITE?
    515 The Canadian Mineralogist Vol. 44, pp. 515-522 (2006) THE CRYSTAL STRUCTURE OF Pb8O5(OH)2Cl4, A SYNTHETIC ANALOGUE OF BLIXITE? SERGEY V. KRIVOVICHEV§ Department of Crystallography, St. Petersburg State University, University Emb. 7/9, RU–199034 St. Petersburg, Russia PETER C. BURNS Department of Civil Engineering and Geological Sciences, University of Notre Dame, Notre Dame, Indiana 46556-0767, USA ABSTRACT The crystal structure of hydrothermally synthesized Pb8O5(OH)2Cl4 [monoclinic, C2/c, a 26.069(5), b 5.8354(11), c 22.736(4) 3 Å, ␤ 102.612(6)°, V 3375.3(11) Å ] has been determined and refi ned to R1 = 0.047 with data collected from a crystal twinned on (100). There are eight symmetrically independent Pb2+ cations in the structure, with each having a strongly distorted coordina- tion polyhedron due to the presence of stereochemically active pairs of s2 lone electrons on the Pb2+ cations. The structure is based upon [O5Pb8] sheets parallel to (100) formed by edge-sharing (OPb4) oxocentered tetrahedra. Hydroxyl groups form two short (OH)–Pb bonds that result in (OH)Pb2 dimers attached to the [O5Pb8] sheets. The chlorine anions are located between the {[O5Pb8](OH)2} sheets, providing three-dimensional linkage of the structure. The structure is closely related to other structures based on PbO-type defect sheets. On the basis of chemical composition and powder X-ray-diffraction data, we suggest that Pb8O5(OH)2Cl4 is a synthetic analogue of blixite. Keywords: lead oxide chloride, blixite, oxocentered tetrahedra, crystal structure. SOMMAIRE Nous avons déterminé et affi né la structure cristalline du composé Pb8O5(OH)2Cl4, synthétisé par voie hydrothermale [mono- 3 clinique, C2/c, a 26.069(5), b 5.8354(11), c 22.736(4) Å, ␤ 102.612(6)°, V 3375.3(11) Å ], jusqu’à un résidu R1 de 0.047 avec des données prélevées sur un cristal maclé sur (100).
    [Show full text]
  • Damaraite, a New Lead Oxychloride Mineral from the Kombat Mine, Namibia (South West Africa)
    Damaraite, a new lead oxychloride mineral from the Kombat mine, Namibia (South West Africa) A. J. CRIDDLE,l P. KELLER,2 C. J. STANLEY' and J. INNES3 IDepartment of Mineralogy, The Natural History Museum, Cromwell Rd., London SW7 5BD, U.K. 2Institut flir Mineralogie und Kristallchemie, Universitat Stuttgart, 0-700 Stuttgart, Germany 3CSIRO Division of Exploration Geoscience, Private Bag, Wembley, Western Australia 6014 Abstract Damaraite, ideally 3PbO.PbCI2, is a new mineral which occurs with jacobsite, hausmannite, hemato- phanite, native copper, an unnamed Pb-Mo oxychloride, calcite, and baryte, in specimens from the Asis West section of the Kombat mine, Namibia (South West Africa). Damaraite is colourless and transparent with a white streak, and adamantine lustre. It is brittle with an irregular to subconchoi- dal fracture and a cleavage on (010). The mineral has a low reflectance, a weak bireflectance, barely discernible reflectance pleochroism, from grey to slightly bluish grey in some sections, and is weakly anisotropic. Reflectance data in air and in oil are tabulated. Colour values relative to the CIE illuminant C for the most strongly bireflectant grain are, for R I and R2 respectively: Y%15.9, 16.9; Ad475, 472; Pe %5.3, 8.9 It has a VHN50 of 148 (range 145-154) with a calculated Mohs hardness of 3. X-ray powder diffraction studies give the following parameters refined from the powder data: orthorhombic; space group Pma2, Pmam or P2]am; a 15.104(1), b 6.891(1), c 5.806 (1)A; V is 604.3 (4)A3 and Z=3. Deale7.84 g/cm3.
    [Show full text]
  • The Crystal Structure of a Mineral Related to Paulkerrite
    Zeitschrift fUr Kristallographie 208, 57 -71 (1993) @ by R. Oldenbourg Verlag, Munchen 1993 ~ 0044-2968/93 $ 3.00+ 0.00 The crystal structure of a mineral related to paulkerrite F. Demartin Istituto di Chimica Strutturistica Inorganica, Universita degli Studi, via Vcnczian 21,1-20133 Milano, Italy T. Pilati CNR, Centro per 10 Studio delle Relazioni tra Struttura e Reattivita Chimica, via Goigi 19, 1-20133 Milano, Italy H. D. Gay Departamento de Geologia, Universidad Nacional de Cordoba, Cordoba, Argentina and C. M. Gramaccioli Dipartimento di Scienze della Terra, Sezione di Mineralogia, Universita degli Studi, via Botticelli 23, 1-20133 Milano, Italy Received: July 24,1992; accepted December 21,1992 Phosphates / Paulkerrite / Mantienneite / Benyacarite / Crystal structure Abstract. An apparently new phosphate mineral (named "benyacarite") showing evident relationships with paulkerrite and mantienneite, but richer in Mn + 2, was found in granitic pegmatites in Argentina (Cerro Blanco, Tanti, Cordoba) where it is associated with other phosphates such as tri- plite etc., and fluorides such as pachnolite. The unit-cell parameters are: ao = 10.561(5) A, bo = 20.585(8) A, CO= 12.516(2) A, orthorhombic, space group Pbca, Z = 4, Dx = 2.37 gcm - 3. The crystal structure has been refined to R(unweighted) = 0.034 and R(weighted) = 0.040 using 1023 independent reflections. It contains layers perpendicular to [010] of two kinds of octahedra, M(2)Os(0,F) and TiOs(O,F), the first essentially centered by Fe+3 atoms, with some Ti+4; the fluorine atom shares vertices of both octahedra. On both sides of these layers there are P04 tetrahedra, with one face approximately parallel to the layers; the three corners of this face are shared with octahedra centered on Ti and M(2), whereas the remaining one is shared with another M(1)06 octahedron centered by 58 F.
    [Show full text]
  • A Specific Gravity Index for Minerats
    A SPECIFICGRAVITY INDEX FOR MINERATS c. A. MURSKyI ern R. M. THOMPSON, Un'fuersityof Bri.ti,sh Col,umb,in,Voncouver, Canad,a This work was undertaken in order to provide a practical, and as far as possible,a complete list of specific gravities of minerals. An accurate speciflc cravity determination can usually be made quickly and this information when combined with other physical properties commonly leads to rapid mineral identification. Early complete but now outdated specific gravity lists are those of Miers given in his mineralogy textbook (1902),and Spencer(M,i,n. Mag.,2!, pp. 382-865,I}ZZ). A more recent list by Hurlbut (Dana's Manuatr of M,i,neral,ogy,LgE2) is incomplete and others are limited to rock forming minerals,Trdger (Tabel,l,enntr-optischen Best'i,mmungd,er geste,i,nsb.ildend,en M,ineral,e, 1952) and Morey (Encycto- ped,iaof Cherni,cal,Technol,ogy, Vol. 12, 19b4). In his mineral identification tables, smith (rd,entifi,cati,onand. qual,itatioe cherai,cal,anal,ys'i,s of mineral,s,second edition, New york, 19bB) groups minerals on the basis of specificgravity but in each of the twelve groups the minerals are listed in order of decreasinghardness. The present work should not be regarded as an index of all known minerals as the specificgravities of many minerals are unknown or known only approximately and are omitted from the current list. The list, in order of increasing specific gravity, includes all minerals without regard to other physical properties or to chemical composition. The designation I or II after the name indicates that the mineral falls in the classesof minerals describedin Dana Systemof M'ineralogyEdition 7, volume I (Native elements, sulphides, oxides, etc.) or II (Halides, carbonates, etc.) (L944 and 1951).
    [Show full text]
  • 31 May 2013 2013-024 Yeomanite
    Title Yeomanite, Pb2O(OH)Cl, a new chain-structured Pb oxychloride from Merehead Quarry, Somerset, England Authors Turner, RW; Siidra, OI; Rumsey, MS; Polekhovsky, YS; Kretser, YL; Krivovichev, SV; Spratt, J; Stanley, Christopher Date Submitted 2016-04-04 2013-024 YEOMANITE CONFIDENTIAL INFORMATION DEADLINE: 31 MAY 2013 2013-024 YEOMANITE Pb2O(OH)Cl Orthorhombic Space group: Pnma a = 6.585(10) b = 3.855(6) c = 17.26(1) Å V = 438(1) Å3 Z = 4 R.W. Turner1*, O.I. Siidra2, M.S. Rumsey3, Y.S. Polekhovsky4, S.V. Krivovichev2, Y.L. Kretser5, C.J. Stanley3, and J. Spratt3 1The Drey, Allington Track, Allington, Salisbury SP4 0DD, Wiltshire, UK 2Department of Crystallography, Geological Faculty, St Petersburg State University, University Embankment 7/9, St Petersburg 199034, Russia 3Department of Earth Sciences, Natural History Museum, Cromwell Road, London SW7 5BD, UK 4Department of Mineral Deposits, St Petersburg State University, University Embankment 7/9, 199034 St Petersburg, Russia 5V.G. Khlopin Radium Institute, Roentgen Street 1, 197101 St Petersburg, Russia *E-mail: [email protected] OCCURRENCE The mineral occurs in the Torr Works (Merehead) Quarry, East Cranmore, Somerset, UK. Yeomanite is associated with mendipite, as a cavity filling in manganese oxide pods. Other oxyhalide minerals that are found hosted in mendipite include diaboleite, chloroxiphite and paralaurionite. Secondary Pb and Cu minerals, including mimetite, wulfenite, cerussite, hydrocerussite, malachite, and crednerite also occur in the same environment. Gangue minerals associated with mineralised manganese pods include aragonite, calcite and barite. Undifferentiated pod-forming Mn oxides are typically a mixture of manganite and pyrolusite, associated with Fe oxyhydroxides such as goethite (Turner, 2006).
    [Show full text]
  • Mn,Fe)5(PO4)2(HPO4)2(H2O)4
    Eur. J. Mineral. 2016, 28, 93–103 Special issue dedicated to Published online 16 June 2015 Thomas Armbruster Single-crystal neutron diffraction and Mo¨ssbauer spectroscopic study of hureaulite, (Mn,Fe)5(PO4)2(HPO4)2(H2O)4 1,2, 3 1,4 5 6 G. DIEGO GATTA *,GU¨ NTHER J. REDHAMMER ,PIETRO VIGNOLA ,MARTIN MEVEN and GARRY J. MCINTYRE 1 Dipartimento di Scienze della Terra, Universita` degli Studi di Milano, Via Botticelli 23, 20133 Milano, Italy 2 CNR - Istituto di Cristallografia, Via G. Amendola 122/o, Bari, Italy *Corresponding author, e-mail: [email protected] 3 Abteilung fu¨r Mineralogie, FB Materialforschung & Physik, Universita¨t Salzburg, Hellbrunnerstr. 34/III, 5020 Salzburg, Austria 4 CNR-Istituto per la Dinamica dei Processi Ambientali, Milano, Italy 5 Institut fu¨r Kristallographie, RWTH Aachen, and Ju¨lich Centre for Neutron Science (JCNS), Forschungszentrum Ju¨lich GmbH, at Heinz Maier-Leibnitz Zentrum (MLZ), Lichtenbergstasse 1, 85748 Garching, Germany 6 Australian Nuclear Science and Technology Organization, Locked Bag 2001, Kirrawee DC NSW 2232, Australia Abstract: The crystal chemistry of hureaulite from the Joca˜o (Cigana) pegmatite, Conselheiro Pena, Doce Valley, Minas Gerais (Brazil), was investigated by electron microprobe analysis in wavelength-dispersive mode, single-crystal Laue (at 293 K) and monochro- 57 M(1),M(2),M(3) 2þ 2þ P P(2) matic neutron diffraction (at 2.3 K), and Fe-Mo¨ssbauer spectroscopy [ (Mn 3.61Fe 1.21Ca0.11Mg0.03) ¼4.96( PO4)2 P(1) ˚ ˚ 3 (H1.04 PO4)2(H2O)3.92, Z ¼ 4, a ¼ 17.603(6), b ¼ 9.087(2), c ¼ 9.404(4) A, b ¼ 96.66(4) , and V ¼ 1494.1(9) A at 293 K, space group C2/c].
    [Show full text]