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Empressite, Agte, from the Empress-Josephine Mine, Colorado, U.S.A.: Composition, Physical Properties, and Determination of the Crystal Structure
American Mineralogist, Volume 89, pages 1043–1047, 2004 Empressite, AgTe, from the Empress-Josephine mine, Colorado, U.S.A.: Composition, physical properties, and determination of the crystal structure LUCA BINDI,1,* PAUL G. SPRY,2 AND CURZIO CIPRIANI1 1 Museo di Storia Naturale, Sezione di Mineralogia, Università degli Studi di Firenze, Via La Pira, 4 I-50121 Firenze, Italy 2 Department of Geological and Atmospheric Sciences, 253 Science I, Iowa State University, Ames, Iowa 50011-3210, U.S.A. ABSTRACT The chemistry and composition of empressite, AgTe, a rare silver telluride mineral, has been mistaken in the mineralogical literature for the silver telluride stützite (Ag5–xTe3). Empressite from the type locality, the Empress-Josephine deposit (Colorado), occurs as euhedral prismatic grains up to 400 μm in length and contains no inclusions or intergrowths with other minerals. It is pale bronze in color and shows a grey-black to black streak. No cleavage is observed in empressite but it shows an uneven to subconchoidal 2 fracture and Vickers hardness (VHN25) of 142 kg/mm . Empressite is greyish white in color, with strong bireflectance and pleochroism. Reflectance percentages forR min and Rmax are 40.1, 45.8 (471.1 nm), 39.6, 44.1 (548.3 nm), 39.4, 43.2 (586.6 nm), and 38.9, 41.8 (652.3 nm), respectively. Empressite is orthorhombic and belongs to space group Pmnb (Pnma as standard), with the fol- lowing unit-cell parameters: a = 8.882(1), b = 20.100(5), c = 4.614(1) Å, V = 823.7(3) Å3, and Z = 16. -
Washington State Minerals Checklist
Division of Geology and Earth Resources MS 47007; Olympia, WA 98504-7007 Washington State 360-902-1450; 360-902-1785 fax E-mail: [email protected] Website: http://www.dnr.wa.gov/geology Minerals Checklist Note: Mineral names in parentheses are the preferred species names. Compiled by Raymond Lasmanis o Acanthite o Arsenopalladinite o Bustamite o Clinohumite o Enstatite o Harmotome o Actinolite o Arsenopyrite o Bytownite o Clinoptilolite o Epidesmine (Stilbite) o Hastingsite o Adularia o Arsenosulvanite (Plagioclase) o Clinozoisite o Epidote o Hausmannite (Orthoclase) o Arsenpolybasite o Cairngorm (Quartz) o Cobaltite o Epistilbite o Hedenbergite o Aegirine o Astrophyllite o Calamine o Cochromite o Epsomite o Hedleyite o Aenigmatite o Atacamite (Hemimorphite) o Coffinite o Erionite o Hematite o Aeschynite o Atokite o Calaverite o Columbite o Erythrite o Hemimorphite o Agardite-Y o Augite o Calciohilairite (Ferrocolumbite) o Euchroite o Hercynite o Agate (Quartz) o Aurostibite o Calcite, see also o Conichalcite o Euxenite o Hessite o Aguilarite o Austinite Manganocalcite o Connellite o Euxenite-Y o Heulandite o Aktashite o Onyx o Copiapite o o Autunite o Fairchildite Hexahydrite o Alabandite o Caledonite o Copper o o Awaruite o Famatinite Hibschite o Albite o Cancrinite o Copper-zinc o o Axinite group o Fayalite Hillebrandite o Algodonite o Carnelian (Quartz) o Coquandite o o Azurite o Feldspar group Hisingerite o Allanite o Cassiterite o Cordierite o o Barite o Ferberite Hongshiite o Allanite-Ce o Catapleiite o Corrensite o o Bastnäsite -
New Mineral Names*,†
American Mineralogist, Volume 104, pages 625–629, 2019 New Mineral Names*,† DMITRIY I. BELAKOVSKIY1 AND FERNANDO CÁMARA2 1Fersman Mineralogical Museum, Russian Academy of Sciences, Leninskiy Prospekt 18 korp. 2, Moscow 119071, Russia 2Dipartimento di Scienze della Terra “Ardito Desio”, Universitá di degli Studi di Milano, Via Mangiagalli, 34, 20133 Milano, Italy IN THIS ISSUE This New Mineral Names has entries for 8 new minerals, including fengchengite, ferriperbøeite-(Ce), genplesite, heyerdahlite, millsite, saranchinaite, siudaite, vymazalováite and new data on lavinskyite-1M. FENGCHENGITE* X-ray diffraction pattern [d Å (I%; hkl)] are: 7.186 (55; 110), 5.761 (44; 113), 4.187 (53; 123), 3.201 (47; 028), 2.978 (61; 135). 2.857 (100; 044), G. Shen, J. Xu, P. Yao, and G. Li (2017) Fengchengite: A new species with 2.146 (30; 336), 1.771 (36; 24.11). Single-crystal X-ray diffraction data the Na-poor but vacancy-dominante N(5) site in the eudialyte group. shows the mineral is trigonal, space group R3m, a = 14.2467 (6), c = Acta Mineralogica Sinica, 37 (1/2), 140–151. 30.033(2) Å, V = 5279.08 Å3, Z = 3. The structure was solved by direct methods and refined to R = 0.043 for all unique I > 2σ(I) reflections. Fengchengite (IMA 2007-018a), Na Ca (Fe3+,) Zr Si (Si O ) 12 3 6 3 3 25 73 Fenchengite is the Fe3+ analog of eudialyte with a structural difference (H O) (OH) , trigonal, is a new eudialyte-group mineral discovered in 2 3 2 in vacancy dominant N5 site and splitting its Na site N1 into N1a and the agpaitic nepheline syenites and its pegmatite facies near the Saima N1b sites. -
Spiridonovite, (Cu1-Xagx)2Te (X ≈ 0.4), a New Telluride from the Good Hope Mine, Vulcan, Colorado (U.S.A.)
minerals Article Spiridonovite, (Cu1-xAgx)2Te (x ≈ 0.4), a New Telluride from the Good Hope Mine, Vulcan, Colorado (U.S.A.) Marta Morana 1 and Luca Bindi 2,* 1 Dipartimento di Scienze della Terra e dell’Ambiente, Università di Pavia, Via A. Ferrata 7, I-27100 Pavia, Italy; [email protected] 2 Dipartimento di Scienze della Terra, Università degli Studi di Firenze, Via G. La Pira 4, I-50121 Firenze, Italy * Correspondence: luca.bindi@unifi.it; Tel.: +39-055-275-7532 Received: 7 March 2019; Accepted: 22 March 2019; Published: 24 March 2019 Abstract: Here we describe a new mineral in the Cu-Ag-Te system, spiridonovite. The specimen was discovered in a fragment from the cameronite [ideally, Cu5-x(Cu,Ag)3+xTe10] holotype material from the Good Hope mine, Vulcan, Colorado (U.S.A.). It occurs as black grains of subhedral to anhedral morphology, with a maximum size up to 65 µm, and shows black streaks. No cleavage is −2 observed and the Vickers hardness (VHN100) is 158 kg·mm . Reflectance percentages in air for Rmin and Rmax are 38.1, 38.9 (471.1 nm), 36.5, 37.3 (548.3 nm), 35.8, 36.5 (586.6 nm), 34.7, 35.4 (652.3 nm). Spiridonovite has formula (Cu1.24Ag0.75)S1.99Te1.01, ideally (Cu1-xAgx)2Te (x ≈ 0.4). The mineral is trigonal and belongs to the space group P-3c1, with the following unit-cell parameters: a = 4.630(2) Å, c = 22.551(9) Å, V = 418.7(4) Å 3, and Z = 6. -
Preliminary Results of Hydrothermal Alteration Assemblage
Preliminary Results of Hydrothermal Alteration Assemblage Classification in Aurora and Bodie Mining Districts, Nevada and California, with Airborne Hyperspectral Data Amer Smailbegovic, James V. Taranik and Wendy M. Calvin Arthur Brant Laboratory for Exploration Geophysics University of Nevada, Reno ABSTRACT The Aurora and Bodie mining districts are located in Bodie Hills, north of Mono Lake, on opposite sides of the Nevada-California state line. From the standpoint of economic geology, both deposits are structurally controlled, low-sulfidation, adularia-sericite precious metal vein deposits with an extensive alteration halo. The area was exploited from the late 1870’s until 1988 by both underground and minor open pit operations (Aurora), exposing portions of ore-hosting altered andesites, devitrified rhyolites as well as quartz-adularia-sericite veins. Much of the geologic mapping and explanation was ad- hoc and primarily in support of the mining operations, without particular interest paid to the system as a whole. The University of Nevada, Reno has acquired both high- and low- altitude AVIRIS data of the region. Low-altitude data was acquired in July 2000, followed by high-altitude collection in October 2000. The AVIRIS coverage was targeted on the main vein system in Aurora (Prospectus and Humboldt Vein), East Brawley Peak prospect (midpoint between Aurora and Bodie) and “Bonanza Zone” (Bodie Bluff and Standard Hill) in Bodie, where the hydrothermal alteration zones appear to be the most pervasive. The ground-observations and mining/prospecting reports suggest propylitic alteration throughout the Bodie Hills, argillic and potassic alteration in Aurora and Bodie, (low-sulfidation system) and alunitic alteration (high-sulfidation system) on East Brawley Peak. -
Acanthite Ag2s C 2001-2005 Mineral Data Publishing, Version 1 Crystal Data: Monoclinic, Pseudo-Orthorhombic
Acanthite Ag2S c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic, pseudo-orthorhombic. Point Group: 2/m. Primary crystals are rare, prismatic to long prismatic, elongated along [001], to 2.5 cm, may be tubular; massive. Commonly paramorphic after the cubic high-temperature phase (“argentite”), of original cubic or octahedral habit, to 8 cm. Twinning: Polysynthetic on {111}, may be very complex due to inversion; contact on {101}. Physical Properties: Cleavage: Indistinct. Fracture: Uneven. Tenacity: Sectile. Hardness = 2.0–2.5 VHN = 21–25 (50 g load). D(meas.) = 7.20–7.22 D(calc.) = 7.24 Photosensitive. Optical Properties: Opaque. Color: Iron-black. Streak: Black. Luster: Metallic. Anisotropism: Weak. R: (400) 32.8, (420) 32.9, (440) 33.0, (460) 33.1, (480) 33.0, (500) 32.7, (520) 32.0, (540) 31.2, (560) 30.5, (580) 29.9, (600) 29.2, (620) 28.7, (640) 28.2, (660) 27.6, (680) 27.0, (700) 26.4 ◦ Cell Data: Space Group: P 21/n. a = 4.229 b = 6.931 c = 7.862 β =99.61 Z=4 X-ray Powder Pattern: Synthetic. 2.606 (100), 2.440 (80), 2.383 (75), 2.836 (70), 2.583 (70), 2.456 (70), 3.080 (60) Chemistry: (1) (2) (3) Ag 86.4 87.2 87.06 Cu 0.1 Se 1.6 S 12.0 12.6 12.94 Total 100.0 99.9 100.00 (1) Guanajuato, Mexico; by electron microprobe. (2) Santa Lucia mine, La Luz, Guanajuato, Mexico; by electron microprobe. (3) Ag2S. Polymorphism & Series: The high-temperature cubic form (“argentite”) inverts to acanthite at about 173 ◦C; below this temperature acanthite is the stable phase and forms directly. -
Revised Version the Crystal Structure of Uytenbogaardtite, Ag3aus2, And
Title The crystal structure of uytenbogaardtite, Ag3AuS2, and its relationships with gold and silver sulfides-selenides Authors Bindi, L; Stanley, Christopher; Seryotkin, YV; Bakakin, VR; Pal'yanova, GA; Kokh, KA Date Submitted 2017-03-30 1 1 1237R – revised version 2 The crystal structure of uytenbogaardtite, Ag3AuS2, and its relationships 3 with gold and silver sulfides-selenides 4 1, 2 3,4 5 5 LUCA BINDI *, CHRISTOPHER J. STANLEY , YURII V. SERYOTKIN , VLADIMIR V. BAKAKIN , 3,4 3,4 6 GALINA A. PAL’YANOVA , KONSTANTIN A. KOKH 7 8 1Dipartimento di Scienze della Terra, Università di Firenze, Via G. La Pira 4, I-50121Firenze, Italy 9 2Natural History Museum, Cromwell Road, London SW7 5BD, United Kingdom 3 10 Sobolev Institute of Geology and Mineralogy of the Siberian Branch of the Russian Academy of Sciences, pr. 11 Akademika Koptyuga, 3, Novosibirsk 630090, Russia 4 12 Novosibirsk State University, Pirogova str., 2, Novosibirsk 630090, Russia 5 13 Institute of Inorganic Chemistry, Siberian Branch of the RAS, prosp. Lavrentieva 3, 630090 Novosibirsk, Russia 14 15 * e-mail address: [email protected] 16 17 Abstract 18 The crystal structure of the mineral uytenbogaardtite, a rare silver-gold sulfide, was solved 19 using intensity data collected on a crystal from the type locality, the Comstock lode, Storey 20 County, Nevada (U.S.A.). The study revealed that the structure is trigonal, space group R 3 c, 3 21 with cell parameters: a = 13.6952(5), c = 17.0912(8) Å, and V = 2776.1(2) Å . The refinement 22 of an anisotropic model led to an R index of 0.0140 for 1099 independent reflections. -
Studies of Minerat Sutpho-Salts
STUDIESOF MINERATSUTPHO-SALTS: XIX_SEIENIANPOTYBASITE D. C. HARRIS.I E. W. NUFFIELD'2 eno M. H. FROHBERGB Ansrnecr A study of a rich Au-Ag ore from the La Guadalupe Arcos mine, Zacualpan, Mexico has led to the discovety of, selenian polybasite associated with a number of silver- bearing minerals. A cleavable variety of pyrite is a feature of the ore. The mineral occurs ur *i"""t" grains but about L milligram was concentrated from a more favourable material from the Sln Carlos mine, Guanajuato, Mexico. This gave the cell dimensions: o 13.00' b 7.5D, c 11.99A, p 90" and, by ,-ray spectroscopy, the approximate cell contents: (Agzs.eCus.z)'--flti" (Sb:.oAsr.e) (Srr.oSeo.o). 6*La-i. aiectasri'ncation of the polybasite-pearceite_minerals.Frondel's -7.5, classification"i"dv into two series, according to whether the cell is small (a*13, b c - L2), or double this, is unienable. The basic structural unit and external crystal fo-rm is the Lme for all polybasites and pearceites. Doubled dimensions, which manifest themselves as weak lntermediate layer lines on rotation photographs, represent less- tlan-fundamental differences. This is illustrated by a coarsely-crystallized specimen from the Las Chispas mine, Mexico. Someareas give the small cell while other, seemingly- ;aentlc.t areas give an intermediate cell (o - 26,b - L5, c - 12). Frondel has reported that-ihe material from this mine gives the double cell. original classification iilo one series,with polybasite as the Sb ) As end-member rnd peardite as the As analogue, is preferable becauseit recognizesthe basic similarity of af potybarite-pearceite mirlrai". -
Intergrowth Texture in Au-Ag-Te Minerals from Sandaowanzi Gold Deposit, Heilongjiang Province: Implications for Ore-Forming Environment
Article Geology July 2012 Vol.57 No.21: 27782786 doi: 10.1007/s11434-012-5170-7 SPECIAL TOPICS: Intergrowth texture in Au-Ag-Te minerals from Sandaowanzi gold deposit, Heilongjiang Province: Implications for ore-forming environment XU Hong*, YU YuXing, WU XiangKe, YANG LiJun, TIAN Zhu, GAO Shen & WANG QiuShu School of Earth Sciences and Resources, China University of Geosciences, Beijing 100083, China Received January 16, 2012; accepted March 16, 2012; published online May 6, 2012 Sandaowanzi gold deposit, Heilongjiang Province, is the only single telluride type gold deposit so far documented in the world, in which 90% of gold is hosted in gold-silver telluride minerals. Optical microscope observation, scanning electron microscope, electron probe and X-ray diffraction analysis identified abundant intergrowth textures in the Au-Ag-Te minerals, typified by sylvanite-hosting hessite crystals and hessite-hosting petzite crystals. The intergrown minerals and their chemistry are consistent, and the hosted minerals are mostly worm-like or as oriented stripes, evenly distributed in the hosting minerals, with clear and smooth interfaces. These suggest an exsolution origin for the intergrowth texture. With reference to the phase-transformation temperature derived from synthesis experiments of tellurides, the exsolution texture of Au-Ag-Te minerals implies that the veined tellurides formed at 150–220°C. The early stage disseminated tellurides formed at log f(Te2) from 13.6 to 7.8, log f(S2) from 11.7 to 7.6, whereas the late stage veined tellurides formed at log f(Te2) ranging from 11.2 to 9.7 and log f(S2) from 16.8 to 12.2. -
By Michael Fleischer and Constance M. Schafer Open-File Report 81
U.S. DEPARTMENT OF THE INTERIOR GEOLOGICAL SURVEY THE FORD-FLEISCHER FILE OF MINERALOGICAL REFERENCES, 1978-1980 INCLUSIVE by Michael Fleischer and Constance M. Schafer Open-File Report 81-1174 This report is preliminary and has not been reviewed for conformity with U.S. Geological Survey editorial standards 1981 The Ford-Fleischer File of Mineralogical References 1978-1980 Inclusive by Michael Fleischer and Constance M. Schafer In 1916, Prof. W.E. Ford of Yale University, having just published the third Appendix to Dana's System of Mineralogy, 6th Edition, began to plan for the 7th Edition. He decided to create a file, with a separate folder for each mineral (or for each mineral group) into which he would place a citation to any paper that seemed to contain data that should be considered in the revision of the 6th Edition. He maintained the file in duplicate, with one copy going to Harvard University, when it was agreed in the early 1930's that Palache, Berman, and Fronde! there would have the main burden of the revision. A number of assistants were hired for the project, including C.W. Wolfe and M.A. Peacock to gather crystallographic data at Harvard, and Michael Fleischer to collect and evaluate chemical data at Yale. After Prof. Ford's death in March 1939, the second set of his files came to the U.S. Geological Survey and the literature has been covered since then by Michael Fleischer. Copies are now at the U.S. Geological Survey at Reston, Va., Denver, Colo., and Menlo Park, Cal., and at the U.S. -
On the Symmetry and Crystal Structure of Aguilarite, Ag4ses
Mineralogical Magazine, February 2013, Vol. 77(1), pp. 21–31 On the symmetry and crystal structure of aguilarite, Ag4SeS 1,2, 3 L. BINDI * AND N. E. PINGITORE 1 Dipartimento di Scienze della Terra, Universita`degli Studi di Firenze, Via G. La Pira 4, I-50121 Firenze, Italy 2 CNR À Istituto di Geoscienze e Georisorse, Sezione di Firenze, Via G. La Pira 4, I-50121 Firenze, Italy 3 Department of Geological Sciences, The University of Texas at El Paso, El Paso, TX-79968-0555 Texas, USA [Received 10 December 2012; Accepted 9 January 2013; Associate Editor: Giancarlo Della Ventura] ABSTRACT An examination of a specimen of aguilarite from the type locality provides new data on the chemistry and structure of this mineral. The chemical formula of the crystal used for the structural study is (Ag3.98Cu0.02)(Se0.98S0.84Te0.18), on the basis of 6 atoms. The mineral was found to be monoclinic, ˚ crystallizing in space group P21/n, with a = 4.2478(2), b = 6.9432(3), c = 8.0042(5) A, b = 100.103(2)º, ˚ 3 V = 232.41(2) A and Z = 4. The crystal structure [refined to R1 = 0.0139 for 958 reflections with I >2s(I)] is topologically identical to that of acanthite, Ag2S. It can be described as a body-centred array of tetrahedrally coordinated X atoms (X = S, Se and Te) with Ag2X3 triangles in planes nearly parallel to (010); the sheets are linked by the Ag1 silver site, which has twofold coordination. Aguilarite is definitively proved to be isostructural with acanthite; it does not have a naumannite-like structure, as previously supposed. -
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).