2015 Mining and Mineral Symposium
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The Black Hills Hydrology Study —By Janet M
Prepared in cooperation with the South Dakota Department of Environment and Natural Resources and the West Dakota Water Development District The Black Hills Hydrology Study —By Janet M. Carter, Daniel G. Driscoll, and Joyce E. Williamson o Introduction 104o 45' 103 30' Indian Horse o Belle Fourche EXPLANATION 44 45' Reservoir Cr The Black Hills area is an impor- Owl Newell Outcrop of Madison Limestone BELLE Creek Creek tant resource center that provides an Nisland Outcrop of Minnelusa Formation F BELLE FOURCHE OU economic base for western South RCHE RIVER Approximate extent of the Black Hay Creek R E BUTTE CO Vale Hills area, represented by Dakota through tourism, agriculture, I V ER R MEADE CO REDWAT LAWRENCE CO generalized outer extent of the timber, and mineral resources. Water Cox the outcrop of Inyan Kara Saint Creek Lake Crow Onge Group originating from the area is used for Creek reek municipal, industrial, agricultural, and 30' Gulch Spearfish C Whitewood Bear x Gulch Butte Bottom Creek e recreational purposes throughout ls Bear a Creek F Whitewood Butte Higgins much of western South Dakota. The Cr Creek Squ STURGIS Spearfish a Central Tinton Cr w li Iron CityCr ka ood DEADWOOD l o Black Hills area also is an important Cr w A 103 ad 15' Beaver Cr e D Cr Lead Bear h nnie Cr s A berry recharge area for aquifers in the north- i traw f S r Cr Creek Tilford a hitetail e W p Cheyenne Elk S ern Great Plains. Crossing Little Creek Roubaix ek Creek N Elk re Elk Little C Population growth, resource devel- . -
Download PDF About Minerals Sorted by Mineral Name
MINERALS SORTED BY NAME Here is an alphabetical list of minerals discussed on this site. More information on and photographs of these minerals in Kentucky is available in the book “Rocks and Minerals of Kentucky” (Anderson, 1994). APATITE Crystal system: hexagonal. Fracture: conchoidal. Color: red, brown, white. Hardness: 5.0. Luster: opaque or semitransparent. Specific gravity: 3.1. Apatite, also called cellophane, occurs in peridotites in eastern and western Kentucky. A microcrystalline variety of collophane found in northern Woodford County is dark reddish brown, porous, and occurs in phosphatic beds, lenses, and nodules in the Tanglewood Member of the Lexington Limestone. Some fossils in the Tanglewood Member are coated with phosphate. Beds are generally very thin, but occasionally several feet thick. The Woodford County phosphate beds were mined during the early 1900s near Wallace, Ky. BARITE Crystal system: orthorhombic. Cleavage: often in groups of platy or tabular crystals. Color: usually white, but may be light shades of blue, brown, yellow, or red. Hardness: 3.0 to 3.5. Streak: white. Luster: vitreous to pearly. Specific gravity: 4.5. Tenacity: brittle. Uses: in heavy muds in oil-well drilling, to increase brilliance in the glass-making industry, as filler for paper, cosmetics, textiles, linoleum, rubber goods, paints. Barite generally occurs in a white massive variety (often appearing earthy when weathered), although some clear to bluish, bladed barite crystals have been observed in several vein deposits in central Kentucky, and commonly occurs as a solid solution series with celestite where barium and strontium can substitute for each other. Various nodular zones have been observed in Silurian–Devonian rocks in east-central Kentucky. -
The Behavior of Molybdenum., Tungsten, and Titanium
The behavior of molybdenum, tungsten, and titanium in the porphyry copper environment Item Type text; Dissertation-Reproduction (electronic) Authors Kuck, Peter Hinckley Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 08/10/2021 00:24:06 Link to Item http://hdl.handle.net/10150/565421 THE BEHAVIOR OF MOLYBDENUM., TUNGSTEN, AND TITANIUM IN THE PORPHYRY COPPER ENVIRONMENT Peter' 'Hinckley Kuck A Dissertation Submitted to the Faculty of the DEPARTMENT OF GEOSCIENCES. In Partial.Fulfillment of the Requirements. ' ■ For the Degree of DOCTOR OF PHILOSOPHY In the Graduate College ■ THE UNIVERSITY OF ARIZONA 1 9 7 8 THE UNIVERSITY OF ARIZONA GRADUATE COLLEGE I hereby recommend that this dissertation prepared under my Peter Hinckley Kuck direction by ___________ , , The Behavior of Molybdenum, Tungsten, and Titanium entitled ________________________________________________________ in the Porphyry Copper Environment be accepted as fulfilling the dissertation requirement for the Doctor of Philosophy degree of _______________________________________________________ Dissertation Director Date As members of the Final Examination Committee, we certify that we have read this dissertation and agree that it may be presented for final defense. \ R A j r i A hi / 7IT 2 / 1 r 7 - Final approval and acceptance of this dissertation is contingent on the candidate's adequate performance and defense thereof at the final oral examination. STATEMENT BY AUTHOR This dissertation has been submitted in partial fulfillment of requirements for an advanced degree at The University of Arizona and is deposited in the University Library to be made available to borrowers under rules of. -
Metamorphism of Sedimentary Manganese Deposits
Acta Mineralogica-Petrographica, Szeged, XX/2, 325—336, 1972. METAMORPHISM OF SEDIMENTARY MANGANESE DEPOSITS SUPRIYA ROY ABSTRACT: Metamorphosed sedimentary deposits of manganese occur extensively in India, Brazil, U. S. A., Australia, New Zealand, U. S. S. R., West and South West Africa, Madagascar and Japan. Different mineral-assemblages have been recorded from these deposits which may be classi- fied into oxide, carbonate, silicate and silicate-carbonate formations. The oxide formations are represented by lower oxides (braunite, bixbyite, hollandite, hausmannite, jacobsite, vredenburgite •etc.), the carbonate formations by rhodochrosite, kutnahorite, manganoan calcite etc., the silicate formations by spessartite, rhodonite, manganiferous amphiboles and pyroxenes, manganophyllite, piedmontite etc. and the silicate-carbonate formations by rhodochrosite, rhodonite, tephroite, spessartite etc. Pétrographie and phase-equilibia data indicate that the original bulk composition in the sediments, the reactions during metamorphism (contact and regional and the variations and effect of 02, C02, etc. with rise of temperature, control the mineralogy of the metamorphosed manga- nese formations. The general trend of formation and transformation of mineral phases in oxide, carbonate, silicate and silicate-carbonate formations during regional and contact metamorphism has, thus, been established. Sedimentary manganese formations, later modified by regional or contact metamorphism, have been reported from different parts of the world. The most important among such deposits occur in India, Brazil, U.S.A., U.S.S.R., Ghana, South and South West Africa, Madagascar, Australia, New Zealand, Great Britain, Japan etc. An attempt will be made to summarize the pertinent data on these metamorphosed sedimentary formations so as to establish the role of original bulk composition of the sediments, transformation and reaction of phases at ele- vated temperature and varying oxygen and carbon dioxide fugacities in determin- ing the mineral assemblages in these deposits. -
Geology and Hydrothermal Alteration of the Duobuza Goldrich Porphyry
doi: 10.1111/j.1751-3928.2011.00182.x Resource Geology Vol. 62, No. 1: 99–118 Thematic Articlerge_182 99..118 Geology and Hydrothermal Alteration of the Duobuza Gold-Rich Porphyry Copper District in the Bangongco Metallogenetic Belt, Northwestern Tibet Guangming Li,1 Jinxiang Li,1 Kezhang Qin,1 Ji Duo,2 Tianping Zhang,3 Bo Xiao1 and Junxing Zhao1 1Key Laboratory of Mineral Resources, Institute of Geology and Geophysics, CAS, Beijing, 2Tibet Bureau of Geology and Exploration, Lhasa, Tibet and 3No. 5 Geological Party, Tibet Bureau of Geology and Exploration, Golmu, China Abstract The Duobuza gold-rich porphyry copper district is located in the Bangongco metallogenetic belt in the Bangongco-Nujiang suture zone south of the Qiangtang terrane. Two main gold-rich porphyry copper deposits (Duobuza and Bolong) and an occurrence (135 Line) were discovered in the district. The porphyry-type mineralization is associated with three Early Cretaceous ore-bearing granodiorite porphyries at Duobuza, 135 Line and Bolong, and is hosted by volcanic and sedimentary rocks of the Middle Jurassic Yanshiping Formation and intermediate-acidic volcanic rocks of the Early Cretaceous Meiriqie Group. Simultaneous emplacement and isometric distribution of three ore-forming porphyries is explained as multi-centered mineralization generated from the same magma chamber. Intense hydrothermal alteration occurs in the porphyries and at the contact zone with wall rocks. Four main hypogene alteration zones are distinguished at Duobuza. Early-stage alteration is dominated by potassic alteration with extensive secondary biotite, K-feldspar and magnetite. The alteration zone includes dense magnetite and quartz-magnetite veinlets, in which Cu-Fe-bearing sulfides are present. -
The Atomic Arrangement of Ojuelaite, Znfe~ + (AS04)2(OH)204H20
SHORT COMMUNICATIONS 519 MINERALOGICAL MAGAZINE, JUNE 1996, VOL. 60, PP 519-521 The atomic arrangement of ojuelaite, ZnFe~ + (AS04)2(OH)204H20 John M. Hughes Department of Geology, Erich S. Bloodaxe Miami University, Kyle D. Kobel Oxford, OR 45056, USA John W. Drexler Department of Geological Sciences, University of Colorado, Boulder, CO 80309, USA OJUELAITEwas described from its occurrence at the site in whitmoreite (Moore et at., 1974). Refinement Ojuela mine in Mapimi, Mexico by Cesbron et al. of electron occupancy of the site yielded 28.0 (1981). Those authors suggested that the phase was electrons, as opposed to 29.0 by electron probe, isostructural with whitmoreite (Moore et at., 1974), a supporting the lack of saturation of the site by Zn. It phase of interest because of the unique arrangement of is not known if the iron in the site is Fe2+ or if it is Fe octaheda in its octahedral sheet. Cesbron et at. Fe3+ that is charge-balanced by a mechanism such as (OH) substitution. (1981) also suggested that ojuelaite was isostructural a concomitant 0 =<== with arthurite, CuFd+(As04h(OHh.4H20 (Keller and Table 2 lists atomic coordinates, equivalent Hess, 1978). The common fibrous habit of ojuelaite, isotropic thermal parameters, and bond valence however, has precluded structure determination. sums before hydrogen bonding is calculated; We obtained a specimen of ojuelaite from the type Table 3 lists selected bond lengths. Structure locality that provided a single crystal suitable for factors and anisotropic thermal parameters may be structure determination. The structure study obtained from the editor. confirmed that ojuelaite is isostructural with whitmoreite and arthurite within the large constraints imposed by the requirements of the different TABLE 1. -
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 -
It's Unfair to the People of This Area for Us To
“It’s unfair to the people of this area for us to collect taxes from our customers to help TVA [Tennessee Valley Authority] sell power at a lower price to their customers.” NEIL SIMPSON, President, Black Hills Power and Light Company 60 Expanding Futures on the Great Plains 4 EXPANDING FUTURES ON THE GREAT PLAINS Black Hills Power and Light continued to expand. The company absorbed smaller utilities. It offered power and transmission services to other areas in collaboration with public power agencies and rural electric cooperatives. But tensions with the rural cooperatives were building over territories and customers. As the federal government began to construct dams and hydroelectric facilities on the Missouri River, company officials scrambled to hold onto Black Hills Power and Light’s market and customers. 61 Expanding Futures on the Great Plains Govenor Peter Norbeck’s plan to build a dam dams on the river would revive the state’s proponents of the public power district bill were and hydroelectric facilities on the Missouri River economy. Their efforts to encourage the federal able to convince legislators that new districts after World War I died for lack of sufficient government to build a series of dams gained were needed to secure the power to be generated demand, but the idea lingered in the minds of momentum in 1943 after spring floods caused by Missouri River hydroelectric plants. The public many policymakers in Pierre and Washington, major damage to downstream communities, power district bill passed in 1950. D.C. After drought, depression and war, South especially Omaha, Nebraska. -
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 -
NEW MINERALS It Is Proposed Hereafter to Indicate In.A General Way the Classification of All New Minerals Recoided in This Department
JOURNAL MINERALOGICAL SOCIETY OF AMENICA 63 Dr. Kunz then spoke of the various city localities and the minerals found therein. He stated that the East Side, from 37 to 110 St., probably afforded the most specimens. The various tunnels and their minerals were spoken of. Capt. Miller called attention to the fine collection of Brooklyn Drift Minerals and Rocks in the collection of the Long Island Historical Society. Ife abo mentioned the occurrence of monazite and xenotime crystals, on the Speedway,Harlem River. Dr. Kunz emphasizedthe irnportance of complete records being kept of all finds. Tnou,q,s L Mrr,r,nn, SecretaryPro, Tem. NEW MINERALS It is proposed hereafter to indicate in.a general way the classification of all new minerals recoided in this department. Subdivision will be first into "families," of which nine may be recognized,as listed in the January number (Am. Min.6 (1), 12,1921). Eachfamilywillbe separatedinto "subfamilies " based on special features of composition. This arrangement is tentative and open to modification, and criticism of it will be welcome, [Eo.] FAMILY 2. SULFIDES, ETC. SosreMrr,v 3. Doust,u suLFrDEs oF METALSAND sEMr-METAr,s. I'LTRABASITE V. Rosrcxf and J. Srnnse-Btinu. Ultrabasit, ein neues Mineral aus Freiberg in Sachsen. (Ultrabasite, a new mineral from Freiberg, Saxony). Rozpr.Eeslcd Ako,il. Prag,25, No. 45, 1916;Z. Krgst. Min., 55,43H39, 1920, Neun: From its extremely basic chemical composition. Pnrsrcar, Pnopnnrrus Color black, somewhat grayish; luster metallic; streak black; cleavage none; fracture scaly, with somewhat greasy luster on the surface. H. : 5; sp. gr. -
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. -
Strengite.Pdf
3+ Strengite Fe PO4 • 2H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Orthorhombic. Point Group: 2/m 2/m 2/m. Crystals are variable in habit, may be dominated by {111}, lathlike along [001], or elongated along [100] or [010], to 5 cm, with many forms. Generally radial fibrous, as botryoidal or spherical aggregates and crusts. Twinning: Rarely on {201}. Physical Properties: Cleavage: On {010}, good; on {001}, poor. Hardness = 3.5 D(meas.) = 2.84–2.87 D(calc.) = 2.84 Optical Properties: Transparent to translucent. Color: Purple, violet, pink, peach-blossom- red, carmine, greenish white; may be nearly colorless. Streak: White. Luster: Vitreous. Optical Class: Biaxial (+). Orientation: X = a; Y = c; Z = b. Dispersion: r< v,strong. α = 1.697–1.708 β = 1.708–1.719 γ = 1.741–1.745 2V(meas.) = Moderate to small. Cell Data: Space Group: P cab. a = 10.122(1) b = 9.886(1) c = 8.7233(7) Z = 8 X-ray Powder Pattern: The Kreuzberg, Germany. (ICDD 33–667). 3.114 (100), 4.383 (85), 5.509 (60), 2.546 (50), 3.996 (45), 3.002 (45), 2.949 (45) Chemistry: (1) (2) P2O5 38.24 37.99 Fe2O3 43.40 42.73 H2O 18.89 19.28 Total 100.53 100.00 • (1) Pleystein, Germany. (2) FePO4 2H2O. Polymorphism & Series: Dimorphous with phosphosiderite, forms a series with variscite. Mineral Group: Variscite group. Occurrence: A late secondary mineral in complex granite pegmatites; in “limonite” iron ores and gossans; with magnetite iron ores; rarely a cave mineral. Association: Beraunite, hur´eaulite,dufr´enite,bermanite, stewartite, cacoxenite, rockbridgeite, vivianite, apatite, leucophosphite, phosphosiderite.