Silver-Rich Central Idaho
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Large-Scale Hydrothermal Zoning Reflectedin The
Canadian Mineralogist Vol. 27, pp. 383-400 (1989) LARGE-SCALE HYDROTHERMAL ZONING REFLECTED IN THE TETRAHEDRITE-FREIBERGITE SOLID SOLUTION, KENO HILL Ag-Pb-Zn DISTRICT, YUKON J.V. GREGORY LYNCH* Department of Geology, The University of Alberta, Edmonton, Alberta T6G 2E3 ABSTRACT en argent se distinguent aussi par une augmentation dans Ie nombre de cations dans leur formule chimique. Le rap- The zoned Keno Hill vein system of central Yukon port Sb/ As demeure uniformement eleve. extends laterally from a Cretaceous plutonic-metamorphic center and surrounding quartz-feldspar veins, to (Traduit par la Redaction) carbonate-Ag-Pb-Zn deposits, and further to peripheral veins having epithermal characteristics. Seven distinct Mots-cles: zonation hydrothermale, nappe aquifere, tetra- mineralogical zones are recognized, and the entire sequence edrite, solution solide, plutonique, epithermal, altera- is continuous from east to west in a 4O-km belt. The fault- tion, district de Keno Hill, Yukon. and fracture-controlled veins are stratabound to the brit- tle moderately dipping Keno Hill Quartzite unit, of Mis- INTRODUCTION sissippian age. The unit is graphitic and appears to have acted as a large-scale hydrothermal aquifer, restricting fluid This paper concerns the large-scale nature of the flow during minera1ization and" development of zoning predominantly to the lateral direction. Tetrahedrite is dis- Keno Hill hydrothermal system. A broad and con- tributed along a 25-km-Iong portion of the system, and is tinuous sequence of mineral zoning can be the principal ore mineral of Ag. Both Ag/Cu and Fe/Zn documented within veins distributed along an exten- values in tetrahedrite are highest at the outer extremity of sive portion of the Keno Hill Quartzite, which is the the system, where freibergite dominates over tetrahedrite; main host rock to the ore in the area. -
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 -
PHASE CHANGES in Cu 2 S AS a FUNCTION of TEMPERATURE 1. PREVIOUS WORK
National Bureau of Standards Special Publication 364, Solid State Chemistry, Proceedings of 5th Materials Research Symposium, issued July 1972. PHASE CHANGES IN cu2s AS A FUNCTION OF TEMPERATURE William R. Cook, Jr. Gould Inc., Gould Laboratories Cleveland, Ohio 44108 and Case Western Reserve University Cleveland, Ohio 44106 The high-'copper phase boundary of Cu2s deviates from stoichiometry above 300 °C, first becoming copper deficient, then above - 1075 °C becoming copper rich. The maximum copper content occurs at the monotectic temperature of 1104 °C. The strong effect of oxygen on the hexagonal-cubic transition in Cu2S was confirmed; the transition was also found to be sensi tive to the type of pretreatment of the material. The high temperature tetragonal "Cu1 96s" phase is stable between Cu1.95S and Cu2s, at temperatures of - 90° to - 140 °C. The tr~nsi tion to the tetragonal phase is extremely sluggish. The true composition of djurleite has been shown to be approximately Cu1.93S. The phases near the chalcocite-digenite region of the diagram may be grouped into those with hexagonal close packing of sulfur atoms and those with cubic close packing of sulfurs. This is important in understanding rates of transformation among the various phases that occur in this area of the diagram. Key words: Chalcocite; cu2s; digenite; djurleite; nonstoichiometry; phase relations. 1. PREVIOUS WORK Fairly thorough explorations of the Cu-s phase diagram between cu2s and cu1• ,shave been made by a number of previous workers [1-8] 1 The resulting diagram may be seen in figure 1 taken largely from Roseboom [7] and Riu [8]. -
Gomposition and Occurrence of Electrum Atthe
L37 The Canadian M inerala g i st Vol.33,pp. 137-151(1995) GOMPOSITIONAND OCCURRENCEOF ELECTRUM ATTHE MORNINGSTAR DEPOSIT, SAN BERNARDINOCOUNTY, GALIFORNIA: EVIDENCEFOR REMOBILIZATION OF GOLD AND SILVER RONALD WYNN SIIEETS*, JAMES R. CRAIG em ROBERT J. BODNAR Depanmen of Geolngical Sciences, Virginin Polytechnic h stitate and Stale (Jniversity, 4A44 Dening Hall, Blacl<sburg, Virginin 24060, U.S-A,. Arsrnacr Elecfum, acanthiteand uytenbogaardtite have been examined from six depthswithin the tabular quartzt calcite sockwork and breccia-filled veins in the fault-zone-hostedMorning Star depositof the northeasternMojave Desert, Califomia. Six distinct types of electrum have been identified on the basis of minerat association,grain moryhology and composition. Two types, (1) p1'rite-hostedand (2) quartz-hostedelectrum, occur with acanthite after argentite and base-metalsulfide minerals in unoxidized portions of the orebody; the remaining forr types, (3) goethite-hostedelectrum, (4) electnrm cores, (5) electrumrims and (6) wire electrum,are associatedwith assemblagesof supergeneminerals in its oxidizedportions. Pyrite- hosted quartz-hostedand goethite-hostedelectrum range in compositionfrom 6l ta 75 utt.7oAu and have uniform textures and no zoning. In lower portions ofthe oxidized ore zone, electrum seemsto replacegoethite and occursas small grains on surfacesof the goethite.Textural evidencefavors supergeneremobilization of Au and Ag, which were depositedas electrum on or replacinggoethite. This type of electrumis identical in appearanceand compositionto prinary electrum,In the upper portions of the oxidized zone,secondary electum occursas a gold-rich rim on a core of elechum and as wire-like grains,both with acanthiteand uytenbogaardtite.Such secondaryelectrum contains from 78 to 93 wt./o Au. Textural relations and asso- ciated minerals suggestthat the primary electrum was hydrothermally depositedand partially remobilized by supergene processes. -
Silver Enrichment in the San Juan Mountains, Colorado
SILVER ENRICHMENT IN THE SAN JUAN MOUNTAINS, COLORADO. By EDSON S. BASTIN. INTRODUCTION. The following report forms part of a topical study of the enrich ment of silver ores begun by the writer under the auspices of the United States Geological Survey in 1913. Two reports embodying the results obtained at Tonopah, Nev.,1 and at the Comstock lode, Virginia City, Nev.,2 have previously been published. It was recognized in advance that a topical study carried on by a single investigator in many districts must of necessity be less com prehensive than the results gleaned more slowly by many investi gators in the course of regional surveys of the usual types; on the other hand the advances made in the study of a particular topic in one district would aid in the study of the same topic in the next. In particular it was desired to apply methods of microscopic study of polished specimens to the ores of many camps that had been rich silver producers but had not been studied geologically since such methods of study were perfected. If the results here reported appear to be fragmentary and to lack completeness according to the standards of a regional report, it must be remembered that for each district only such information could be used as was readily obtainable in the course of a very brief field visit. The results in so far as they show a primary origin for the silver minerals in many ores appear amply to justify the work in the encouragement which they offer to deep mining, irrespective of more purely scientific results. -
Supergene Mineralisation of the Boyongan Porphyry Copper-Gold Deposit, Surigao Del Norte, Philippines
Supergene Mineralisation of the Boyongan Porphyry Copper-Gold Deposit, Surigao del Norte, Philippines by Allan Maglaya Ignacio B.Sc. Geology, National Institute of Geological Sciences University of the Philippines Thesis submitted in partial fulfilment of the requirements of the Masters of Economic Geology Degree Centre for Ore Deposit Research, University of Tasmania December, 2005 DECLARATION OF ORIGINALITY This thesis contains no material which has been accepted for a degree of diploma by the University of Tasmania or any other institution, except by way of background information and duly acknowledged in the thesis, and contains no previous material previously pub- lished or written by another person except where due acknowledgement is given. Allan Maglaya Ignacio 01 December 2005 _________________________ STATEMENT OF AUTHORITY OF ACCESS This thesis may not to be made available for loan or copying for 1.5 years following the date this statement was signed. Following that time, the thesis may be available for loan and lim- ited copying in accordance with Copyright Act 1968. Allan Maglaya Ignacio 01 December 2005 _________________________ TABLE OF CONTENTS Page (s) LIST OF FIGURES …………………………………………………….. i - iii LIST OF APPENDICES ………………………………………………… iv ACKNOWLEDGMENTS ………………………………………………. v ABSTRACT ……………………………………………………………... vi - vii 1.0 INTRODUCTION ………………………………………………………. 1 - 8 1.1 Introduction …………………………………………………………. 1 1.2 Aims and Objectives ……………………………………………….. 1 1.3 Methods Employed …………………………………………………. 2 1.4 Location and Accessibility …………………………………………. 3 1.5 Climate ……………………………………………………………... 5 1.6 Previous Work ……………………………………………………… 5 2.0 GEOLOGICAL SETTING ………………………………………………. 9 - 37 2.1 Introduction ………………………………………………………. 9 2.2 Regional Tectonics …………….…………………………………. 9 2.3 Regional and Local Stratigraphy ………………………………... 11 2.3.1 Basement (Cretaceous-Paleogene) ………………………. 11 2.3.2 Bacuag Formation (Oliogocene-Miocene) .…………….. -
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. -
Porphyry Deposits
PORPHYRY DEPOSITS W.D. SINCLAIR Geological Survey of Canada, 601 Booth St., Ottawa, Ontario, K1A 0E8 E-mail: [email protected] Definition Au (±Ag, Cu, Mo) Mo (±W, Sn) Porphyry deposits are large, low- to medium-grade W-Mo (±Bi, Sn) deposits in which primary (hypogene) ore minerals are dom- Sn (±W, Mo, Ag, Bi, Cu, Zn, In) inantly structurally controlled and which are spatially and Sn-Ag (±W, Cu, Zn, Mo, Bi) genetically related to felsic to intermediate porphyritic intru- Ag (±Au, Zn, Pb) sions (Kirkham, 1972). The large size and structural control (e.g., veins, vein sets, stockworks, fractures, 'crackled zones' For deposits with currently subeconomic grades and and breccia pipes) serve to distinguish porphyry deposits tonnages, subtypes are based on probable coproduct and from a variety of deposits that may be peripherally associat- byproduct metals, assuming that the deposits were econom- ed, including skarns, high-temperature mantos, breccia ic. pipes, peripheral mesothermal veins, and epithermal pre- Geographical Distribution cious-metal deposits. Secondary minerals may be developed in supergene-enriched zones in porphyry Cu deposits by weathering of primary sulphides. Such zones typically have Porphyry deposits occur throughout the world in a series significantly higher Cu grades, thereby enhancing the poten- of extensive, relatively narrow, linear metallogenic tial for economic exploitation. provinces (Fig. 1). They are predominantly associated with The following subtypes of porphyry deposits are Mesozoic to Cenozoic orogenic belts in western North and defined according to the metals that are essential to the eco- South America and around the western margin of the Pacific nomics of the deposit (metals that are byproducts or poten- Basin, particularly within the South East Asian Archipelago. -
MENDELSOHN (F.), Editor. the Geology of the Northern Rhodesian Copper- Belt
996 BOOK REVIEWS instance 'pits', ' anisotropy', ' cellular texture', ' native iron', are fol- lowed by a 'text-card' with a more detailed description of the sections concerned in English and German. The price is DM 0.75 per photo-card, DM 0.45 per text-card. These prices are reduced by 10% for University departments and academic staff, by 15% for students. The great value of this unique publication is self-evident and does not need further appraisal. Ore-microscopists will welcome the card index as a high-quality source of reference, and university staff will find it a great help in teaching. Economic geologists and nfineralogists will appreciate the straightforward and clear approach, which provides an excellent introduction for research workers less well acquainted with the subject matter. Ore dressing workers and metallurgists will be able to Use the card index for the solution of their problems without having to go into details of ore mineralogy. The authors should be warmly con- gratulated on this first part of a very fine piece of work. A. F. H. MENDELSOHN (F.), editor. The Geology of the Northern Rhodesian Copper- belt. London (Macdonald & Co. Ltd.), 1961, xvi+523 pp., 185 figs. Price 8r Twenty-three authors have contributed to this comprehensive volume. Part 1 provides a general account of the physiography, stratigraphy, structure, metamorphism, and ore deposits of the Copperbelt together with a history of mineral exploration and an account of the methods employed. Part 2 gives detailed descriptions of the individual deposits. In addition to synthesizing the considerable volume of published work on the subject the authors draw extensively on material from unpublished company reports. -
New Mineral Names*,†
American Mineralogist, Volume 104, pages 1360–1364, 2019 New Mineral Names*,† DMITRIY I. BELAKOVSKIY1, FERNANDO CÁMARA2, AND YULIA UVAROVA3 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 3CSIRO Mineral Resources, ARRC, 26 Dick Perry Avenue, Kensington, Western Australia 6151, Australia IN THIS ISSUE This New Mineral Names has entries for 9 new minerals, including argentotetrahedrite-(Fe), bytízite, calamaite, fluorlamprophyllite, honzaite, katerinopoulosite, meitnerite, melcherite, and rozhdestvenskayaite-(Zn). ARGENTOTETRAHEDRITE [-(FE)]* AND 460 31.0 / 30.3, 31.5, 33.7; 480 30.9 / 30.1, 31.3, 33.5; 500 30.8 33.2 ROZHDESTVENSKAYAITE [-(ZN)]* 31.2 29.7; 520 30.8 / 29.1, 31.1, 33.0, 540 30.7 / 28.2, 31.0, 32.7; 560 M.D. Welch, C.J. Stanley, J. Spratt and S.J. Mills (2018) 30.7 / 27.1, 31.0, 32.4, 580 30.6 / 26.0, 30.9, 32.0, 600 30.4 / 25.0, 30.8, 31.6; 620 30.3 / 24.3, 30.5, 31.2; 640 30.1 / 23.5, 30.2, 30.8; 660 29.9 / Rozhdestvenskayaite Ag10Zn2Sb4S13 and argentotetrahedrite 2+ 23.1, 30.0, 30.5; 680 29.7 / 22.9, 29.8, 30.3; 700 29.6 / 22.7, 29.7, 30.1. Ag6Cu4(Fe ,Zn)2Sb4S13: two Ag-dominant members of the tetra- hedrite group. European Journal of Mineralogy, 30(6), 1163–1172. The averages of electron probe WDS analysis of “four tetrahedrites” [i.e. -
Mineralogy, Textures, and Relative Age Relationships of Massive Sulfide Ore in the West Shasta District, California
Econom/cGeo/og• Vol. 80, 1985, pp. 2114-2127 Mineralogy, Textures, and Relative Age Relationshipsof MassiveSulfide Ore in the West ShastaDistrict, California STEPHEN S. HOWE U.S. GeologicalSurvey, 345 MiddlefieldRoad, Mail Stop901, Menlo Park, California 94025 Abstract The Devonian massive sulfide orebodies of the West Shasta district in northern California are composedprimarily of pyrite, with lesseramounts of other sulfideand gangueminerals. Examinationof polishedthin sectionsof more than 100 samplesfrom the Mammoth,Shasta King, Early Bird, Balaklala,Keystone, and Iron Mountainmines suggests that mineralization may be dividedinto six parageneticstages, the last five each separatedby an episodeof deformation:(1) precipitationof fine-grained,locally colloformand framboidalpyrite and sphalerite;(2) depositionof fine-grainedarsenopyrite and coarse-grainedpyrite, the latter enclosingtiny inclusionsof pyrrhotite;(3) penetrationand local replacement of sulfideminerals of stages1 and 2 alonggrowth zones and fracturesby chalcopyrite,sphalerite, galena, ten- nantite, pyrrhotite, bornite, and idaite; (4) recrystallizationand remobilizationof existing minerals,locally increasingtheir size and euhedralismand promotingtheir aggregation;(5) depositionof quartz, white mica, chlorite, and calcite;and (6) formationof bornite, digenite, chalcocite,and covellite during supergene enrichment of severalorebodies at the Iron Mountain mine.Despite regional greenschist facies metamorphism and local heating by intrusivebodies, enoughof the originaldepositional -
New Discoveries of Rare Minerals in Montana Ore
New discoveries of rare Au and Ag minerals in some Montana ore deposits Chris Gammons Geological Engineering, Montana Tech • Butte • McDonald Meadows • Virginia City District • Elkhorn (Boulder) District Butte • Produced over 600 million oz of silver • 2nd in U.S. to Couer d’Alene district ID • Produced roughly 3 million oz of gold • 2nd in Montana to Golden Sunlight Mine Mining Engineering, Web Exclusive 2016 Mineral (group) Formula Guilbert & Ziehen, 1964 This study HYPOGENE Argentite Ag2SXX Pearceite‐polybasite (Ag,Cu)16(As,Sb)2S11 XX Proustite‐pyrargyrite Ag3(As,Sb)S3 XX Stephanite Ag5SbS4 X Andorite PbAgSb3S6 X Stromeyerite AgCuS X X Ag‐tetrahedrite (Ag,Cu)12Sb4S13 XX Furutobeite (Cu,Ag)6PbS4 X Larosite (Cu,Ag)21(Pb,Bi)2S13 X Matildite AgBiS2 X Jalpaite Ag3CuS2 X Electrum AgAu X Petzite Ag3AuTe2 X Hessite Ag2Te X Empressite (?) AgTe X SUPERGENE Acanthite Ag2SXX Silver Ag X X Cerargyrite AgCl X furotobeite: (Cu,Ag)6PbS4 bornite furutobeite bornite stromeyerite + chalcocite furutobeite Mt. Con mine (AMC # 591) larosite: (Cu,Ag)21(Pb,Bi)2S13 stromeyerite larosite wittichenite Cu3BiS3 strom mawsonite Cu6Fe2SnS8 chalcocite pyrite pyrite bornite MT. Con 5933 Occurrences of furutobeite and larosite: Furutobeite Larosite • None in U.S. • None in U.S. • < 5 locations world‐wide • Butte = 3rd (?) locality • Type locality = Furutobe world‐wide mine, Japan (Kuroko‐type VMS) Fred Larose Early prospector in Cobalt silver camp, Ontario jalpaite: Ag3CuS2 Barite Wittichenite Cu3BiS3 Jalpaite Bornite Jalpaite AMC 4756 Anselmo Mine EPMA‐BSE image Goldfieldite Cu10Te 4S13 Bi‐Cu‐Se‐telluride Tennantite or enargite Emplectite: CuBiS2 Bi‐Cu‐Se‐telluride Hessite (Ag2Te) Empressite (AgTe) St.