Spring 1991 Gems & Gemology Gem News
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38Th RMS Program Notes
E.fu\wsoil 'og PROGRAM Thursday Evening, April 14, 2011 PM 4:00-6:00 Cocktails and Snacks – Hospitality Suite 400 (4th Floor) 6:00-7:45 Dinner – Baxter’s 8:00-9:15 THE GUALTERONI COLLECTION: A TIME CAPSULE FROM A CENTURY AGO – Dr. Renato Pagano In 1950, the honorary curator of the Museum of Natural History in Genoa first introduced Dr. Renato Pagano to mineral collecting as a Boy Scout. He has never looked back. He holds a doctorate in electrical engineering and had a distinguished career as an Italian industrialist. His passion for minerals has produced a collection of more than 13,000 specimens, with both systematic and aesthetic subcollections. His wife Adriana shares his passion for minerals and is his partner in collecting and curating. An excellent profile of Renato, Adriana, and their many collections appeared earlier this year in Mineralogical Record (42:41-52). Tonight Dr. Pagano will talk about an historic mineral collection assembled between 1861 and 1908 and recently acquired intact by the Museum of Natural History of Milan. We most warmly welcome Dr. Renato Pagano back to the speakers’ podium. 9:15 Cocktails and snacks in the Hospitality Suite on the 4th floor will be available throughout the rest of the evening. Dealers’ rooms will be open at this time. All of the dealers are located on the 4th floor. Friday Morning, April 15, 2011 AM 9:00 Announcements 9:15-10:15 CRACKING THE CODE OF PHLOGOPITE DEPOSITS IN QUÉBEC (PARKER MINE), MADAGASCAR (AMPANDANDRAVA) AND RUSSIA (KOVDOR) – Dr. Robert F. Martin Robert François Martin is an emeritus professor of geology at McGill University in Montreal. -
Paragenesis of Thb Newry Pegmatite, Maine H
PARAGENESIS OF THB NEWRY PEGMATITE, MAINE H. J. Fnnsnn, Haroard. Uniaersity. The Dunton tourmaline deposit, which occurs in the town of eral assemblagepresent. The deposit has been briefly described by Bastinl and certain rare phosphatesfound there have been discussedby palache.? The deposit was first opened during the summers of 1903 and 1904in a for commercial quantities of pollucite. satisiactory quantities were obtained but mining has now ceased. Due to the care with which Mr. Nevel collected all unusual minerals, it was possible to secure a very complete suite for the Harvard Mineralogical Museum. This suite formed the basis for the mineralogical data in this paper. Acxnowr,roGMENTs Thc writer wishes to acknowledge his great indebtedness to Professor Palache whoseconstant assistanceand constructive criti- cism were of the utmost value during the collection of the data and the preparation of this paper. professor palache made a crys- tallographic study of the tourmalines and constructed the figuies given in this paper. To Mr. H. Berman the writer is obligated for much assistance during the laboratory study of the minerals and the mineral se- quence, Mr. H. Butterfield visited and studied the Newry deposit in 1927 and the writer has drawn freely on his unpublished data. 34e 350 TH E AM ERIC A N M I N ERA LOGIST LocarroN lies at an elevation of about 1525 feet above sea level and 4600 feet west of the main highway. Mining operations were confined to two outcrops, about 250 feet apart, which occur on the western side of the crest of the hill. DBscnrPtroN or PBGuarrrB The wall rock surrounding the outcrops is a light green mica- schist composed essentially of muscovite, actinolite and quartz' This rock has been much disturbed so that near the outcrops, at least, the direction of schistosity is very variable. -
Koritnigite Zn(Aso3oh)•
Koritnigite Zn(AsO3OH) • H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Triclinic, pseudomonoclinic. Point Group: 1. As imperfect platy crystals, to 5 mm, in aggregates. Physical Properties: Cleavage: {010}, perfect; cleavage traces k [001] and k [100], visible on {010}. Tenacity: Flexible. Hardness = 2 D(meas.) = 3.54 D(calc.) = 3.56 Optical Properties: Transparent. Color: Colorless, white, rose. Luster: Pearly on {010}. Optical Class: Biaxial (+). Orientation: X = b; Y ∧ a ' 28◦; Z ∧ c ' 22◦. α = 1.632(5) β = 1.652(3) γ = 1.693(3) 2V(meas.) = 70(5)◦ Cell Data: Space Group: P 1. a = 7.948(2) b = 15.829(5) c = 6.668(2) α =90.86(2)◦ β =96.56(2)◦ γ =90.05(2)◦ Z=8 X-ray Powder Pattern: Tsumeb, Namibia; very close to cobaltkoritnigite. 7.90 (10), 3.16 (9), 3.83 (7), 2.461 (6), 2.186 (5), 3.95 (4), 2.926 (4) Chemistry: (1) (2) (3) As2O5 51.75 54.67 51.46 FeO + Fe2O3 trace 0.05 CoO 4.54 NiO 2.44 ZnO 35.97 25.83 36.44 MgO trace H2O [12.3] [12.47] 12.10 Total [100.0] [100.00] 100.00 2− (1) Tsumeb, Namibia; by electron microprobe, (AsO3OH) confirmed by IR, H2O by difference. • (2) J´achymov, Czech Republic; H2O by difference. (3) Zn(AsO3OH) H2O. Occurrence: A secondary mineral of the lower oxidation zone in a dolostone-hosted polymetallic hydrothermal ore deposit (Tsumeb, Namibia). Association: Tennantite, cuprian adamite, stranskiite, lavendulan, k¨ottigite,tsumcorite, prosperite, o’danielite (Tsumeb, Namibia); erythrite, arsenolite, sphalerite (J´achymov, Czech Republic). -
Raman and Infrared Spectroscopic Characterization of Beryllonite, a Sodium and Beryllium Phosphate Mineral – Implications for Mineral Collectors ⇑ Ray L
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 97 (2012) 1058–1062 Contents lists available at SciVerse ScienceDirect Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy journal homepage: www.elsevier.com/locate/saa Raman and infrared spectroscopic characterization of beryllonite, a sodium and beryllium phosphate mineral – implications for mineral collectors ⇑ Ray L. Frost a, , Yunfei Xi a, Ricardo Scholz b, Fernanda M. Belotti c, Luiz Alberto Dias Menezes Filho d a School of Chemistry, Physics and Mechanical Engineering, Science and Engineering Faculty, Queensland University of Technology, GPO Box 2434, Brisbane Queensland 4001, Australia b Geology Department, School of Mines, Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG, 35400-00, Brazil c Federal University of Itajubá, Campus Itabira, Itabira, MG, Brazil d Geology Department, Institute of Geosciences, Federal University of Minas Gerais, Belo Horizonte, MG, 31270-901, Brazil highlights graphical abstract " We have studied the mineral beryllonite. " Be isotopes play an important role in the dating of sediments and in the study of relief evolution. " We have characterized beryllonite using vibrational spectroscopic techniques. " The pegmatitic phosphates are more readily studied by Raman spectroscopy. article info abstract Article history: The mineral beryllonite has been characterized by the combination of Raman spectroscopy and infrared Received 30 May 2012 spectroscopy. SEM–EDX was used for the chemical analysis of the mineral. The intense sharp Raman band Received in revised form 16 July 2012 at 1011 cmÀ1, was assigned to the phosphate symmetric stretching mode. Raman bands at 1046, 1053, Accepted 17 July 2012 1068 and the low intensity bands at 1147, 1160 and 1175 cmÀ1 are attributed to the phosphate antisym- Available online 4 August 2012 metric stretching vibrations. -
Note on Lavendulan from Joachimstal, Bohemia
TOURNAL XIINERALOG}CAL SOCIET'Y OF A]IERICA 29 NOTE ON LAVENDULAN FROM JOACHIMSTAL, BOHEMIA \Vrrrrnu F. Fosnac,l Llnited, Stotes National Museu,m Under the name lavendulan, Breithaupt2 described a mineral from Annaberg in the Erzgebirge' The mineral formed thin crusts of a lavender blue color and botryoidal structure. Sufficient material apparently was not available for a quantitative analysis but the blowpipe characteristics were determined by Plattner' The collection of Colonel Washington A. Roebling contains a specimen of lavendulan from Joachimstal which probably repre- sents the same mineral described by Breithaupt. It is entirely similar in general appearances and blowpipe characteristics to the Annaberg material. The lavendulan forms very thin crusts with botryoidal surlace upon a seam of qvartz in a mica schist. Its color is patent blue (Ridgeway) with a vitreous to waxy lustre. Although the crust appears amorphous, under the microscopeit is seento be made up of minute radiated fibers or plates. They are slightly pleochroic, the colors being patent to oxide blue. The plates are so small that the optical properties could not be determined with exactness' The followingconstants were measured: B: 1'715+ 005;t: l'725+003' Z is in the direction of the length of the fibers. The extinction is inclined to the length of the fibers. The mineral is distinctly made up of bands of varying composition and the indices of refraction show a corresponding variation. Breithaupt's mineral was essentially a hydrous cobalt arsenate with some copper and nickel. Before the blowpipe the mineral colored the flame light blue (arsenic) and fused easily to a mass that assumedcrystalline form upon cooling. -
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American Mineralogist, Volume 77, pages 670475, 1992 NEW MINERAL NAMES* JonN L. J,Annson CANMET, 555 Booth Street,Ottawa, Ontario KIA OGl' Canada Abswurmbachite* rutile, hollandite, and manganoan cuprian clinochlore. The new name is for Irmgard Abs-Wurmbach, in recog- T. Reinecke,E. Tillmanns, H.-J. Bernhardt (1991)Abs- her contribution to the crystal chemistry, sta- wurmbachite, Cu'?*Mnl*[O8/SiOo],a new mineral of nition of physical properties ofbraunite. Type the braunite group: Natural occurrence,synthesis, and bility relations, and crystal structure.Neues Jahrb. Mineral. Abh., 163,ll7- material is in the Smithsonian Institution, Washington, r43. DC, and in the Institut fiir Mineralogie, Ruhr-Universitlit Bochum, Germany. J.L.J. The new mineral and cuprian braunit€ occur in brown- ish red piemontite-sursassitequartzites at Mount Ochi, near Karystos, Evvia, Greece, and in similar quartzites on the Vasilikon mountains near Apikia, Andros Island, Barstowite* Greece.An electron microprobe analysis (Andros mate- C.J. Stanley,G.C. Jones,A.D. Hart (1991) Barstowite, gave SiO, 9.8, TiO, rial; one of six for both localities) 3PbClr'PbCOr'HrO, a new mineral from BoundsClifl 0.61,Al,O3 0.60, Fe'O, 3.0,MnrO. 71.3,MgO 0.04,CuO St. Endellion,Cornwall. Mineral. Mag., 55, l2l-125. 12.5, sum 97.85 wto/o,corresponding to (CuStrMn3tu- Electron microprobe and CHN analysis gavePb75.47, Mgoo,)", oo(Mn3jrFe|jrAlo orTif.[nCuStr)", nrSi' o, for eight (calc.)6.03, sum 101.46wto/o, cations,ideally CuMnuSiO'r, the Cu analogueof braunite. Cl 18.67,C l.Iz,H 0.18,O to Pb.orClrrrCr.or- The range of Cu2* substitution for Mn2' is 0-42 molo/oin which for 17 atoms corresponds The min- cuprian braunite and 52-93 molo/oin abswurmbachite. -
Mineralogy and Environmental Stability of Slags from the Tsumeb Smelter, Namibia
Applied Geochemistry 24 (2009) 1–15 Contents lists available at ScienceDirect Applied Geochemistry journal homepage: www.elsevier.com/locate/apgeochem Mineralogy and environmental stability of slags from the Tsumeb smelter, Namibia Vojteˇch Ettler a,*, Zdenek Johan b, Bohdan Krˇíbek c, Ondrˇej Šebek d, Martin Mihaljevicˇ a a Institute of Geochemistry, Mineralogy and Mineral Resources, Charles University, Albertov 6, 128 43 Prague 2, Czech Republic b Bureau des Recherches Géologiques et Minières (BRGM), av. Claude Guillemin, 45060 Orléans, cedex 2, France c Czech Geological Survey, Geologická 6, 152 00 Prague 5, Czech Republic d Laboratories of the Geological Institutes, Charles University, Albertov 6, 128 43 Prague 2, Czech Republic article info abstract Article history: Three types of smelting slags originating from historically different smelting technologies in the Tsumeb Received 27 June 2008 area (Namibia) were studied: (i) slags from processing of carbonate/oxide ore in a Cu–Pb smelter (1907– Accepted 22 October 2008 1948), (ii) slags from Cu and Pb smelting of sulphide ores (1963–1970) and (iii) granulated Cu smelting Available online 30 October 2008 slags (1980–2000). Bulk chemical analyses of slags were combined with detailed mineralogical investi- gation using X-ray diffraction analysis (XRD), scanning electron microscopy (SEM/EDS) and electron Editorial handling by R. Fuge microprobe (EPMA). The slags are significantly enriched in metals and metalloids: Pb (0.97–18.4 wt.%), Cu (0.49–12.2 wt.%), Zn (2.82–12.09 wt.%), Cd (12–6940 mg/kg), As (930–75,870 mg/kg) and Sb (67– 2175 mg/kg). Slags from the oldest technology are composed of primary Ca- and Pb-bearing feldspars, spinels, complex Cu–Fe and Cu–Cr oxides, delafossite–mcconnellite phases and Ca–Pb arsenates. -
Mineralogy of Pegmatites
University of New Hampshire University of New Hampshire Scholars' Repository New England Intercollegiate Geological NEIGC Trips Excursion Conference Collection 1-1-1960 Mineralogy of Pegmatites Peacor, D.R. Follow this and additional works at: https://scholars.unh.edu/neigc_trips Recommended Citation Peacor, D.R., "Mineralogy of Pegmatites" (1960). NEIGC Trips. 40. https://scholars.unh.edu/neigc_trips/40 This Text is brought to you for free and open access by the New England Intercollegiate Geological Excursion Conference Collection at University of New Hampshire Scholars' Repository. It has been accepted for inclusion in NEIGC Trips by an authorized administrator of University of New Hampshire Scholars' Repository. For more information, please contact [email protected]. TRIP E MINERALOGY OP PEGMATITES OP THE NEWRY HILL AREA, NEWRY, MAINE Leader: D. R. Peacor Meet at 8:15 A.M., Sunday, October 9, at the base of Plumbago Mountain, on Route 5. The meeting place is easily recognized through the Abbott farmhouse on the east side of the road, and the ore hopper and pas ture on the west side. The one mile long dirt road up to the mines was passable by car on July l6. If it has been washed out by October we will arrange for jeeps to ferry those few who are unable to walk to the top of the hill. INTRODUCTION There are five major quarries in the area (Pig. 1) and many smaller prospect pits. The mineral suites from three of these quarries are different and a unique opportunity to study a wide range of pegmatite minerals is available. -
Geology of the Pegmatites and Associated Rocks of Maine
DEPARTMENT OF THE INTERIOR UNITED STATES GEOLOGICAL SURVEY GEORGE OTIS SMITH, DIRECTOR BULLETIN 445 GEOLOGY OF THE PEGMATITES AND ASSOCIATED ROCKS OF MAINE INCLUDING FELDSPAR, QUARTZ, MICA, AND GEM DEPOSITS BY EDSON S. BASTIN WASHINGTON GOVERNMENT PRINTING OFFICE 1911 CONTENTS. Introduction.............................................................. 9 Definition of pegmatite...................................................... 10 Geographic distribution.................................................... 10 Geology.................................................................. 10 Bordering rocks....................................................... 10 Pegmatites in foliated rocks........................................ 11 General statement............................................ 11 Sedimentary foliates........................................... 11 Igneous foliates.....".......................................... 12 Pegmatites in massive granites.................................... 13 'Age.................................................................. 15 General character..................................................... 15 Mineral and chemical composition................................. 15 Mineral constituents.......................................... 15 Relative proportions of minerals............................... 18 Quartzose phases. ..............................^............. 18 Fluidal cavities............................................... 19 Sodium and lithium phases................................... 20 Muscovite -
30 the AMERICAN MINERALOGIST the Optical Properties of The
30 THE AMERICAN MINERALOGIST The optical properties of the lavendulan are similar to those of erythrite, but with somewhat higher indices. Lavendulan is therefore, probably, the copper analogue of erythrite or simply a cupriferous erythrite. It is so poorly characterized, however, and its homogeneity so uncertain that any definite conclusion as to its relationships is unwarranted. FREIRINITE: A NEW MINERAL SPECIES Wrrrrllr F. Fosnac,l United SlatesNational, Museum The cobalt deposits of San Juan, Chile, have provided a number of specimensof a turquois blue arsenate of copper that have been referred by Goldsmith2 to the mineral lavendulan. Examinatiorr of this mineral and of the lavendulan from Joachimstali has shown that the Chilean mineral is well defined both chemically and physi- cally and entirely distinct from the lavendulan. ft does not cor- respond to any known mineral and the name Jreir,i,ni,te,fuom the locality at which it is found, Department of Freirini, Chile, is proposedfor it. The mineral is found in the Blanca Mine, San Juan, Department of Freirini, Chile. It occurs in a tourmalinized igneous rock as thin, roughly parallel veinlets with scaly, granular or columnar structure. Erythrite is abundantly associatedwith the freirinite in similar veinlets or coatings on cracks. Other associatesare cobaltiferous wad, cuprite and malachite. The original sulphide mineral is cobaltite4but none now remains in the specimenscarrv- ing the freirinite. The freirinite is greenish blue in color (centre blue Ridgeway) with a calamine blue streak. It is made up of fine flakes that give the coarser material a satiny lustre. Under the microscope the mineral is seen to be composed of small plates or columns. -
Roscherite-Group Minerals from Brazil
■ ■ Roscherite-Group Minerals yÜÉÅ UÜté|Ä Daniel Atencio* and José M.V. Coutinho Instituto de Geociências, Universidade de São Paulo, Rua do Lago, 562, 05508-080 – São Paulo, SP, Brazil. *e-mail: [email protected] Luiz A.D. Menezes Filho Rua Esmeralda, 534 – Prado, 30410-080 - Belo Horizonte, MG, Brazil. INTRODUCTION The three currently recognized members of the roscherite group are roscherite (Mn2+ analog), zanazziite (Mg analog), and greifensteinite (Fe2+ analog). These three species are monoclinic but triclinic variations have also been described (Fanfani et al. 1977, Leavens et al. 1990). Previously reported Brazilian occurrences of roscherite-group minerals include the Sapucaia mine, Lavra do Ênio, Alto Serra Branca, the Córrego Frio pegmatite, the Lavra da Ilha pegmatite, and the Pirineus mine. We report here the following three additional occurrences: the Pomarolli farm, Lavra do Telírio, and São Geraldo do Baixio. We also note the existence of a fourth member of the group, an as-yet undescribed monoclinic Fe3+-dominant species with higher refractive indices. The formulas are as follows, including a possible formula for the new species: Roscherite Ca2Mn5Be4(PO4)6(OH)4 • 6H2O Zanazziite Ca2Mg5Be4(PO4)6(OH)4 • 6H2O 2+ Greifensteinite Ca2Fe 5Be4(PO4)6(OH)4 • 6H2O 3+ 3+ Fe -dominant Ca2Fe 3.33Be4(PO4)6(OH)4 • 6H2O ■ 1 ■ Axis, Volume 1, Number 6 (2005) www.MineralogicalRecord.com ■ ■ THE OCCURRENCES Alto Serra Branca, Pedra Lavrada, Paraíba Unanalyzed “roscherite” was reported by Farias and Silva (1986) from the Alto Serra Branca granite pegmatite, 11 km southwest of Pedra Lavrada, Paraíba state, associated with several other phosphates including triphylite, lithiophilite, amblygonite, tavorite, zwieselite, rockbridgeite, huréaulite, phosphosiderite, variscite, cyrilovite and mitridatite. -
Andradite in Andradite Unusual Growth Zoning in Beryl
Editor Nathan Renfro Contributing Editors Elise A. Skalwold and John I. Koivula Andradite in Andradite ity, but size was not what made it special. As shown in fig- Recently we had the opportunity to examine a dramatic ure 1, close examination of one of the polished crystal faces iridescent andradite fashioned by Falk Burger (Hard Works, revealed a bright reddish orange “hot spot” in the center, Tucson, Arizona) from a crystal originating from the caused by an iridescent inclusion of andradite with a dif- Tenkawa area of Nara Prefecture in Japan. Known as “rain- ferent crystallographic orientation than its host. As seen bow” andradite, this material was previously reported in in figure 2, the inclusion’s different orientation caused the iridescence of the rhomb-shaped “hot spot” to appear and Gems & Gemology (T. Hainschwang and F. Notari, “The cause of iridescence in rainbow andradite from Nara, disappear as the light source was passed over the crystal’s Japan,” Winter 2006, pp. 248–258). The specimen was surface. To see the iridescence from both the host and in- unique for its genesis and optical phenomenon. clusion at the same time, two light sources from opposite Weighing 16.79 ct and measuring 15.41 × 13.86 × 10.49 directions must be used due to the different crystallo- mm, the andradite was very large for its species and local- graphic orientation of the host and inclusion. This elusive optical phenomenon made this Japanese andradite crystal extremely interesting for any aspiring inclusionist. John I. Koivula Figure 1. This 16.79 ct Japanese andradite garnet GIA, Carlsbad exhibits a very unusual rhomb-shaped “hot spot” below the surface of one crystal face.