Mineralization of the Hansonburg Mining District, Bingham, New Mexico John Rakovan and Frederick Partey, 2009, Pp
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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. -
CREEDITE from NEVADA Wrrrrrlr F. Fosnac,L Uni.Ted. States Ivati.Onal
CREEDITE FROM NEVADA WrrrrRlr F. Fosnac,l Uni.ted.States IVati.onal Muspum. The mineial creedite was first found by Esper S. Larsen in the fluorite mines of Wagon Wheel Gap, CreedeQuadrangle, Colorado, and describedby Larsen2and Wells as a new mineral speciesof the composition CaSOn.2CaF z. 2AI(F,OH)a. 2HzO. Later, better ma- terial was obtained and the mineral further investigated by the present writerr confirming the composition as found by Wells and determining the crystal symmetry and elements.The mineral was found to be monoclinic. Several crystal habits were found, all pris- matic but differing somewhat in the relative sizes of the terminaL faces. The mineral is associated with fluorite or embedded in a white halloysite clay. During geological field work for the U. S. Geological Survey in the Tonopah Quadrangle,Nevada, Mr. StanleyH. Cathcart visited the small gold camp of Granite (now abandoned), northwest of Tonopah in the northwestern corner of the Tonopah quadrangle and collected some specimensof the high grade ore found in the small veins of the district. These specimens showed scattered bunchesof a colorlessprismatic mineral which were determined by Dr. Clarence S. Ross, from their optical properties, to be creedite. The specimens were then turned over to the present writer for further study and are now in the collections of the U. S. National Museum (No.96489). The two specimens suggest that the gold bearing deposits of Granite are fluorite-quartz veins with free gold. The specimensare from the oxidized zone and are discolored by a clayey manganese wad. Visible flakes of gold are embedded both in the wad and in the fluorite. -
Plumbogummite Pbal3(PO4)2(OH)5 • H2O C 2001-2005 Mineral Data Publishing, Version 1
Plumbogummite PbAl3(PO4)2(OH)5 • H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Hexagonal. Point Group: 32/m. Crystals hexagonal or bladed, prismatic, to 5 mm, in parallel to subparallel aggregates; microscopically radially fibrous or spherulitic; usually as crusts, botryoidal, reniform, stalactitic, globular, compact massive. Physical Properties: Fracture: Uneven to subconchoidal. Tenacity: Brittle. Hardness = 4.5–5 D(meas.) = 4.01 D(calc.) = [4.08] Optical Properties: Transparent to translucent. Color: Grayish white, grayish blue, yellowish gray, yellowish brown, green, pale blue. Streak: White. Luster: Vitreous, resinous to dull. Optical Class: Uniaxial (+); segments of crystals may be biaxial. ω = 1.653–1.688 = 1.675–1.704 Cell Data: Space Group: R3m. a = 7.017(1) c = 16.75(1) Z = 3 X-ray Powder Pattern: Ivanhoe mine, Australia. 2.969 (10), 5.71 (9), 2.220 (8), 3.51 (7), 1.905 (6), 3.44 (5), 4.93 (4) Chemistry: (1) (2) SO3 0.67 P2O5 22.47 24.42 As2O5 0.04 Al2O3 25.45 26.32 Fe2O3 0.01 CuO 0.92 PbO 38.90 38.41 H2O [11.54] 10.85 Total [100.00] 100.00 1− (1) Ivanhoe mine, Australia; by electron microprobe, H2O by difference, (OH) • confirmed by IR; leading to Pb1.02Cu0.07Al2.92[(PO4)1.85(SO4)0.05]Σ=1.90(OH)5.29 0.73H2O. • (2) PbAl3(PO4)2(OH)5 H2O. Mineral Group: Crandallite group. Occurrence: An uncommon secondary mineral in the oxidized zone of lead deposits. Association: Pyromorphite, mimetite, duftite, cerussite, anglesite, wulfenite. Distribution: In France, from Huelgoat, Finist`ere.In England, from Roughton Gill, Red Gill, Dry Gill, and other mines, Caldbeck Fells, Cumbria; in Cornwall, from Wheal Gorland, Gwennap; at the Penberthy Croft mine, St. -
Mineralogical Study of the Advanced Argillic Alteration Zone at the Konos Hill Mo–Cu–Re–Au Porphyry Prospect, NE Greece †
Article Mineralogical Study of the Advanced Argillic Alteration Zone at the Konos Hill Mo–Cu–Re–Au Porphyry Prospect, NE Greece † Constantinos Mavrogonatos 1,*, Panagiotis Voudouris 1, Paul G. Spry 2, Vasilios Melfos 3, Stephan Klemme 4, Jasper Berndt 4, Tim Baker 5, Robert Moritz 6, Thomas Bissig 7, Thomas Monecke 8 and Federica Zaccarini 9 1 Faculty of Geology & Geoenvironment, National and Kapodistrian University of Athens, 15784 Athens, Greece; [email protected] 2 Department of Geological and Atmospheric Sciences, Iowa State University, Ames, IA 50011, USA; [email protected] 3 Faculty of Geology, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece; [email protected] 4 Institut für Mineralogie, Westfälische Wilhelms-Universität Münster, 48149 Münster, Germany; [email protected] (S.K.); [email protected] (J.B.) 5 Eldorado Gold Corporation, 1188 Bentall 5 Burrard St., Vancouver, BC V6C 2B5, Canada; [email protected] 6 Department of Mineralogy, University of Geneva, CH-1205 Geneva, Switzerland; [email protected] 7 Goldcorp Inc., Park Place, Suite 3400-666, Burrard St., Vancouver, BC V6C 2X8, Canada; [email protected] 8 Center for Mineral Resources Science, Department of Geology and Geological Engineering, Colorado School of Mines, 1516 Illinois Street, Golden, CO 80401, USA; [email protected] 9 Department of Applied Geosciences and Geophysics, University of Leoben, Leoben 8700, Austria; [email protected] * Correspondence: [email protected]; Tel.: +30-698-860-8161 † The paper is an extended version of our paper published in 1st International Electronic Conference on Mineral Science, 16–21 July 2018. Received: 8 October 2018; Accepted: 22 October 2018; Published: 24 October 2018 Abstract: The Konos Hill prospect in NE Greece represents a telescoped Mo–Cu–Re–Au porphyry occurrence overprinted by deep-level high-sulfidation mineralization. -
Revision 1 New Insights Into the Crystal Chemistry of Sauconite (Zn
This is the peer-reviewed, final accepted version for American Mineralogist, published by the Mineralogical Society of America. The published version is subject to change. Cite as Authors (Year) Title. American Mineralogist, in press. DOI: https://doi.org/10.2138/am-2020-7460. http://www.minsocam.org/ Revision 1 New insights into the crystal chemistry of sauconite (Zn-smectite) from the Skorpion zinc deposit (Namibia) via a multi-methodological approach Emanuela Schingaro1*, Gennaro Ventruti1, Doriana Vinci1, Giuseppina Balassone2, Nicola Mondillo2, Fernando Nieto3, Maria Lacalamita1, Matteo Leoni4,5 1Dipartimento di Scienze della Terra e Geoambientali, Università degli Studi di Bari Aldo Moro, Via Orabona 4, I-70125, Bari, Italy 2Dipartimento di Scienze della Terra dell’Ambiente e delle Risorse, Università “Federico II”, Complesso Universitario Monte S. Angelo, Via Cintia, I-80126, Napoli, Italy 3Departamento de Mineralogía y Petrología, IACT, Universidad de Granada-CSIC, Av. Fuentenueva s/n, 18002, Granada, Spain 4Saudi Aramco Research and Development Center, P.O. Box 5000, 31311, Dhahran, Saudi Arabia 5Dipartimento di Ingegneria Civile, Ambientale e Meccanica, Università di Trento, Via Mesiano, 77, Trento, 38123, Italy *Corresponding author: Emanuela Schingaro, e-mail: [email protected] RUNNING TITLE: New insights into the crystal chemistry of sauconite 1 Always consult and cite the final, published document. See http:/www.minsocam.org or GeoscienceWorld This is the peer-reviewed, final accepted version for American Mineralogist, -
Minerals of the San Luis Valley and Adjacent Areas of Colorado Charles F
New Mexico Geological Society Downloaded from: http://nmgs.nmt.edu/publications/guidebooks/22 Minerals of the San Luis Valley and adjacent areas of Colorado Charles F. Bauer, 1971, pp. 231-234 in: San Luis Basin (Colorado), James, H. L.; [ed.], New Mexico Geological Society 22nd Annual Fall Field Conference Guidebook, 340 p. This is one of many related papers that were included in the 1971 NMGS Fall Field Conference Guidebook. Annual NMGS Fall Field Conference Guidebooks Every fall since 1950, the New Mexico Geological Society (NMGS) has held an annual Fall Field Conference that explores some region of New Mexico (or surrounding states). Always well attended, these conferences provide a guidebook to participants. Besides detailed road logs, the guidebooks contain many well written, edited, and peer-reviewed geoscience papers. These books have set the national standard for geologic guidebooks and are an essential geologic reference for anyone working in or around New Mexico. Free Downloads NMGS has decided to make peer-reviewed papers from our Fall Field Conference guidebooks available for free download. Non-members will have access to guidebook papers two years after publication. Members have access to all papers. This is in keeping with our mission of promoting interest, research, and cooperation regarding geology in New Mexico. However, guidebook sales represent a significant proportion of our operating budget. Therefore, only research papers are available for download. Road logs, mini-papers, maps, stratigraphic charts, and other selected content are available only in the printed guidebooks. Copyright Information Publications of the New Mexico Geological Society, printed and electronic, are protected by the copyright laws of the United States. -
The Geochemistry and Mobility of Zinc in the Regolith. Advances in Regolith 2003 289
Advances in Regolith 2003 287 THE GEOCHEMISTRY AND MOBILITY OF ZINC IN THE REGOLITH D. C. McPhail1, Edward Summerhayes1, Susan Welch1 & Joël Brugger2 CRC LEME, Department of Geology, Australian National University, Canberra, ACT, 0200 1South Australian Museum and Adelaide University, Adelaide, SA 5000 INTRODUCTION The mobility of zinc in the regolith is important for several reasons, including the weathering of zinc deposits, formation of non-sulphide zinc deposits and contamination of soils and waters from human impact. The mobility of zinc is also important more generally to geologists and geochemists, both exploration and otherwise, because of the need to understand the formation of zinc ore deposits, such as Mississippi Valley Type (MVT), volcanic-hosted massive sulphide (VHMS), zinc oxide and others in which zinc occurs. This means that exploration geochemists, economic geologists and environmental scientists need to understand how zinc exists in the regolith, different lithologies and water, how it is mobilized or trapped, how far it can be transported and whether it is bioavailable and acts as either a micronutrient or a toxin to plant and animal life. In economic geology, there is presently an increasing interest in the formation of zinc oxide, or non- sulphide zinc deposits, and this is reflected in a recent special issue in the journal Economic Geology (Sangster 2003). Although the mobility of zinc in the regolith depends on the transporting process (e.g., groundwater advection or convection, sediment or airborne physical transport, biotic), it depends substantially on the geochemistry of zinc, i.e., how does zinc exist in groundwater and the regolith materials and what are the important geochemical reactions between water and solid. -
Aurichalcite (Zn, Cu)5(CO3)2(OH)6 C 2001-2005 Mineral Data Publishing, Version 1
Aurichalcite (Zn, Cu)5(CO3)2(OH)6 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic, pseudo-orthorhombic by twinning. Point Group: 2/m. As acicular to lathlike crystals with prominent {010}, commonly striated k [001], with wedgelike terminations, to 3 cm. Typically in tufted divergent sprays or spherical aggregates, may be in thick crusts; rarely columnar, laminated or granular. Twinning: Observed in X-ray patterns. Physical Properties: Cleavage: On {010} and {100}, perfect. Tenacity: “Fragile”. Hardness = 1–2 D(meas.) = 3.96 D(calc.) = 3.93–3.94 Optical Properties: Transparent to translucent. Color: Pale green, greenish blue, sky-blue; colorless to pale blue, pale green in transmitted light. Luster: Silky to pearly. Optical Class: Biaxial (–). Pleochroism: Weak; X = colorless; Y = Z = blue-green. Orientation: X = b; Y ' a; Z ' c. Dispersion: r< v; strong. α = 1.654–1.661 β = 1.740–1.749 γ = 1.743–1.756 2V(meas.) = Very small. Cell Data: Space Group: P 21/m. a = 13.82(2) b = 6.419(3) c = 5.29(3) β = 101.04(2)◦ Z=2 X-ray Powder Pattern: Mapim´ı,Mexico. 6.78 (10), 2.61 (8), 3.68 (7), 2.89 (4), 2.72 (4), 1.827 (4), 1.656 (4) Chemistry: (1) CO2 16.22 CuO 19.87 ZnO 54.01 CaO 0.36 H2O 9.93 Total 100.39 (1) Utah; corresponds to (Zn3.63Cu1.37)Σ=5.00(CO3)2(OH)6. Occurrence: In the oxidized zones of copper and zinc deposits. Association: Rosasite, smithsonite, hemimorphite, hydrozincite, malachite, azurite. -
Crystal Structure and Compressibility of Lead Dioxide up to 140 Gpa
American Mineralogist, Volume 99, pages 170–177, 2014 Crystal structure and compressibility of lead dioxide up to 140 GPa BRENT GROCHOLSKI1,*, SANG-HEON SHIM2, ELIZABETH COTTRELL1 AND VITALI B. PRAKAPENKA3 1Department of Mineral Sciences, National Museum of Natural History, Smithsonian Institution, 10th and Constitution Avenue, Washington, D.C. 20560, U.S.A. 2School of Earth and Space Exploration, Arizona State University, 781 S. Terrace Road, Tempe, Arizona 85281 U.S.A. 3Center for Advanced Radiation Sources, University of Chicago, 5640 South Ellis Avenue, Chicago, Illinois 60637, U.S.A. ABSTRACT Lead dioxide is an important silica analog that has high-pressure behavior similar to what has been predicted for silica, only at lower pressures. We have measured the structural evolution and compres- sional behavior of different lead dioxide polymorphs up to 140 GPa in the laser-heated diamond-anvil cell using argon as a pressure medium. High-temperature heating prevents the formation of multi-phase mixtures found in a previous study conducted at room temperature using a silicone grease pressure medium. We find diffraction peaks consistent with a baddeleyite-type phase in our cold-compressed samples between 30 and 40 GPa, which was not observed in the previous measurements. Lead dioxide undergoes a phase transition to a cotunnite-type phase at 24 GPa. This phase remains stable to at least 140 GPa with a bulk modulus of 219(3) GPa for K0′ = 4. Decompression measurements show a pure cotunnite-type phase until 10.5 GPa, where the sample converts to a mixture of baddeleyite-type, pyrite-type, and OI-type (Pbca) phases. -
Arsentsumebite Pb2cu(Aso4)(SO4)(OH) C 2001-2005 Mineral Data Publishing, Version 1
Arsentsumebite Pb2Cu(AsO4)(SO4)(OH) c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. As distorted crystals, to 2 mm, in aggregates and crusts. Twinning: Complex, observed. Physical Properties: Fracture: [Uneven] (by analogy to tsumebite). Tenacity: [Brittle.] Hardness = [3.5] D(meas.) = 6.46 D(calc.) = 6.39 Optical Properties: Semitransparent. Color: Grass-green to apple-green. Luster: [Vitreous.] Optical Class: Biaxial (–). Pleochroism: X = pale pistachio-green; Y = Z = bottle-green. α = 1.970 β = 1.992 γ = 2.011 2V(meas.) = 88◦ ◦ Cell Data: Space Group: P 21/m. a = 8.85 b = 5.92 c = 7.84 β = 112.6 Z=2 X-ray Powder Pattern: Tsumeb, Namibia; close to tsumebite. (ICDD 25-456). 3.25 (100), 4.80 (65), 2.76 (60), 3.64 (46), 2.96 (40), 3.01 (32), 2.094 (30) Chemistry: (1) (2) SO3 9.36 10.97 P2O5 0.55 As2O5 13.45 15.74 CuO 10.61 10.90 PbO 61.91 61.16 H2O 1.58 1.23 Total 97.46 100.00 (1) Tsumeb, Namibia; by electron microprobe, As2O5 originally given as As2O3, H2ObyCHN analyzer. (2) Pb2Cu(AsO4)(SO4)(OH). Mineral Group: Brackebuschite group. Occurrence: A rare mineral in the oxidized zone of a dolostone-hosted hydrothermal polymetallic ore deposit (Tsumeb, Namibia); in a hydrothermal polymetallic barite–fluorite deposit (Clara mine, Germany). Association: Malachite, cerussite, azurite, smithsonite, mimetite, bayldonite, conichalcite, duftite, quartz, iron oxide (Tsumeb, Namibia). Distribution: From Tsumeb, Namibia. In the Clara mine, near Oberwolfach, Black Forest, Germany. At Moldava, 20 km northwest of Teplice, Czech Republic. -
Volume 73 Number 2 February 2020
DELVINGS The Newsletter of the Delvers Gem & Mineral Society Volume 73 Number 2 February 2020 Winter is the season to explore our local desert, see the sights and perhaps collect some rocks. This picture was taken at Mosaic Canyon in Death Valley. The name of the canyon refers to a breccia of cemented rock fragments, but perhaps more fascinating is the banded marble shown here, polished by flash floods – the Noonday Dolomite. It is truly ancient, dating back about 750 million years, formed in a shallow sea rich in algae. The limestone was enriched with magnesium (probably by groundwater) transforming it into dolomitic limestone. The enormous pressure and heat of deep burial later transformed this “dolostone” into a marble. Photo by Andrew Hoekstra Delvers Gem & Mineral Society, Inc. - mailing address: 3833 San Anseline, Long Beach, CA 90808 Taps From the Gavel 2020 Board We are off to a great start with the first meeting of the New Year behind President – Marvin Belcher us. During our meeting, we had two separate and informative [email protected] presentations from our members, Dale Harwood and Andrew Hoekstra. VP – Charles Pierce Later in the month, a few of us Delvers took to the road and headed to [email protected] Treasurer – Emmalee Fowler the QIA POW WOW in Quartzite, AZ. The weather was very nice and [email protected] perfect for walking around outside. On Saturday we met up with other Secretary – Judy Belcher rock hounds for a trip to Brenda. We found some collection sites close [email protected] by and looked for Jasper, Agate and Chalcedony roses if you were lucky. -
PPM Bi-Annual Report 2017 & 2018
PPM Bi-Annual Report 2017 & 2018 The Bi-Annual Report for the PPM Research Centre DEPARTMENT OF GEOLOGY UNIVERSITY OF JOHANNESBURG The Bi-annual Report of the PPM Research Centre for the two years 2017 and 2018, compiled by Jan Kramers. Layout and design by UJ Graphic Studio Special thanks/Acknowledgements We wish to extend a special word of thanks to all our corporate and governmental financial and logistical supporters (in alphabetical order): African Rainbow Minerals Anglo American Anglo Coal Anglo Gold Ashanti Anglo Platinum Anglo Research Assmang Assore Coaltech Council of Geoscience Cradle of Humankind Trust of Gauteng De Beers Consolidated Mines Department of Science and Technology (DST) Deutsche Akademische Austauschdienst (DAAD) Golder Associates Impala Platinum Kumba Iron Ore Lonmin National Research Foundation (NRF) Nkomati Joint Venture Rand Uranium (Gold One) Sibanye Stillwater South 32 Two Rivers Platinum Mine Vale Vedanta Resources Please direct all enquiries and proposals for research to: Dr Bertus Smith, Prof. Jan Kramers or Prof. Fanus Viljoen or PPM, Department of Geology University of Johannesburg Auckland Park Kingsway Campus PO Box 524, Auckland Park 2006 Johannesburg, South Africa E-mail: [email protected], [email protected] or [email protected] Tel: +27(0)11 559 4701 Fax: +27(0)11 559 4702 Cover photo: Product being poured at the ferrochrome smelter near Machadodorp. Photo B. Cairncross Header photo: The landscape at Aggeneys, Northern Cape. Photo: Trishya Owen-Smith Footer photo: Stalagmite Phalanx at Cango Caves. Photo: Trishya Owen-Smith Both footer and header photos were taken on the Honours field trip, September 2018.