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Trolleite Al4(PO4)3(OH)3 C 2001-2005 Mineral Data Publishing, Version 1
Trolleite Al4(PO4)3(OH)3 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. Lamellar, massive, to 3 cm. Physical Properties: Cleavage: In two directions, indistinct. Fracture: Even to conchoidal. Hardness = 8.5 D(meas.) = 3.10 D(calc.) = 3.08 Optical Properties: Translucent. Color: Pale green to bright blue. Luster: Vitreous. Optical Class: Biaxial (–). Dispersion: r> v,weak. α = 1.619 β = 1.639 γ = 1.643 2V(meas.) = 49◦ Cell Data: Space Group: I2/c. a = 18.894(5) b = 7.161(1) c = 7.162(2) β =99.99(2)◦ Z=4 X-ray Powder Pattern: Champion mine, California, USA. 3.208 (100), 3.095 (90), 3.075 (50), 2.519 (45), 3.336 (40), 6.667 (35), 1.983 (35) Chemistry: (1) (2) (3) P2O5 46.72 48.00 47.97 Al2O3 43.26 43.87 45.94 Fe2O3 2.75 0.34 CaO 0.97 0.02 H2O 6.23 [7.77] 6.09 Total 99.93 [100.00] 100.00 (1) V¨astan˚amine, Sweden. (2) H¨okens˚as, Sweden; by electron microprobe, total Fe as Fe2O3, H2O by difference. (3) Al4(PO4)3(OH)3. Occurrence: In amphibolite-grade metamorphic rocks. Association: Berlinite, attakolite, augelite, lazulite (V¨astan˚amine, Sweden); scorzalite, augelite, vis´eite(Champion mine, California, USA); montebrasite, scorzalite, bertossaite, brazilianite, apatite, gatumbaite, samuelsonite, wyllieite (Buranga pegmatite, Rwanda). Distribution: In Sweden, from the V¨astan˚amine, near N¨asum,Sk˚ane; at H˚alsj¨oberg, V¨armland;from H¨okens˚as,V¨asterg¨otland.In the Buranga pegmatite, Rwanda. -
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 -
Llallagua Tin Ore Deposit (Bolivia)
resources Article Speculations Linking Monazite Compositions to Origin: Llallagua Tin Ore Deposit (Bolivia) Elizabeth J. Catlos * and Nathan R. Miller Department of Geological Sciences, Jackson School of Geosciences, The University of Texas at Austin, 1 University Sta. C9000, EPS 1.130, Austin, TX 78712, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-512-471-4762 Received: 3 May 2017; Accepted: 25 July 2017; Published: 29 July 2017 Abstract: Monazite [(Ce,Th)PO4] from the Llallagua tin ore deposit in Bolivia is characterized by low radiogenic element contents. Previously reported field evidence and mineral associations suggest the mineral formed via direct precipitation from hydrothermal fluids. Monazite compositions thus may provide insight into characteristics of the fluids from which it formed. Chemical compositions of three Llallagua monazite grains were obtained using Electron Probe Microanalysis (EPMA, n = 64) and laser ablation mass spectrometry (LA-ICP-MS, n = 56). The mineral has higher amounts of U (123 ± 17 ppm) than Th (39 ± 20 ppm) (LA-ICP-MS, ±1σ). Grains have the highest amounts of fluorine ever reported for monazite (0.88 ± 0.10 wt %, EPMA, ±1σ), and F-rich fluids are effective mobilizers of rare earth elements (REEs), Y, and Th. The monazite has high Eu contents and positive Eu anomalies, consistent with formation in a highly-reducing back-arc environment. We speculate that F, Ca, Si and REE may have been supplied via dissolution of pre-existing fluorapatite. Llallagua monazite oscillatory zoning is controlled by an interplay of low (P + Ca + Si + Y) and high atomic number (REE) elements. -
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. -
Winter 2006 Gems & Gemology Gem News
EDITOR Brendan M. Laurs ([email protected]) CONTRIBUTING EDITORS Emmanuel Fritsch, IMN, University of Nantes, France ([email protected]) Henry A. Hänni, SSEF, Basel, Switzerland ([email protected]) Franck Notari, Geneva, Switzerland ([email protected]) Kenneth V. G. Scarratt, GIA Research, Bangkok, Thailand ([email protected]) DIAMONDS Angola and the Democratic Republic of Congo. This situ- Update on Diamond Trading in Sierra Leone. During the ation led to the Kimberley Process for certifying dia- decade-long civil war in Sierra Leone, the Revolutionary monds from mine to market, which was implemented in United Front (RUF) rebel army committed widespread 2002. With the signing of the Lomé Peace Agreement atrocities against innocent civilians, drawing global con- between the Sierra Leone government and the RUF earlier demnation by governments, human rights groups, and that year, peace has returned to the country. concerned citizens. The RUF was partially funded by the In August 2006, GIA Education instructor Ric Taylor country’s diamond resources, bringing the issue of con- traveled through the Sierra Leone diamond mining areas of flict diamonds in Sierra Leone to world attention in the Koidu, Tongo, Kenema, and Bo, some of which were once late 1990s. Meanwhile, similar diamond-funded conflicts controlled by the rebels. He saw no evidence of continuing were being waged in other African nations, such as conflict, and residents and journalists in these areas con- firmed that there is no desire to return to war. In the town of Koidu (figure 1), in the diamond mining district of Kono Figure 1. The town of Koidu, in the Kono district of in eastern Sierra Leone, one can still see the bare walls of eastern Sierra Leone, was at the center of the county’s buildings that were looted and burned, but many others protracted conflict because of the area’s diamond have been rebuilt and have roofs of corrugated metal or resources. -
The Rutile Deposits of the Eastern United States
THE RUTILE DEPOSITS OF THE EASTERN UNITED STATES. By THOMAS L. WATSON. INTRODUCTION. The titanium-bearing minerals comprise more than 60 distinct species, grouped under a variety of mineral and chemical forms, chiefly as oxides, titanates, titano-silicates, silicates, columbates, and iantalates. These minerals are widely distributed in a variety of associations and in such quantity as to make titanium a relatively abundant element. Clarke* estimates the. amount of titanium in the solid crust of the earth to be 0.44 per cent, equivalent in oxide to 0.73 per cent, the element thus standing in the ninth place in the scale of abundance, next to potassium. Most of the titanium-bearing minerals, however, are rare and are only of scientific interest. The largest concentrations of the element are as oxide (rutile), as iron titanate (ilmenite), and in iron ferrate (magnetite) as intergrown ilmenite. Of these three forms the prin cipal source of the element at present is rutile. The known workable deposits of rutile, however, are extremely few and widely sepa rated, and as the demand for titanium has greatly increased in the last few years it has been necessary for some uses to turn to ilmenite or highly titaniferous magnetites. This paper briefly summarizes present knowledge of the geology of the rutile deposits in the eastern United States and for the sake of comparison discusses several foreign deposits, each of which has produced some rutile. Of the known deposits in the United, States only those in Virginia are of commercial importance. These have been made the subject of a special report 2 by the Virginia Geological Survey, which was preceded by a preliminary paper on the rutile deposits of Amherst and Nelson counties.3 1 Clarke, F. -
Mineral Collecting Sites in North Carolina by W
.'.' .., Mineral Collecting Sites in North Carolina By W. F. Wilson and B. J. McKenzie RUTILE GUMMITE IN GARNET RUBY CORUNDUM GOLD TORBERNITE GARNET IN MICA ANATASE RUTILE AJTUNITE AND TORBERNITE THULITE AND PYRITE MONAZITE EMERALD CUPRITE SMOKY QUARTZ ZIRCON TORBERNITE ~/ UBRAR'l USE ONLV ,~O NOT REMOVE. fROM LIBRARY N. C. GEOLOGICAL SUHVEY Information Circular 24 Mineral Collecting Sites in North Carolina By W. F. Wilson and B. J. McKenzie Raleigh 1978 Second Printing 1980. Additional copies of this publication may be obtained from: North CarOlina Department of Natural Resources and Community Development Geological Survey Section P. O. Box 27687 ~ Raleigh. N. C. 27611 1823 --~- GEOLOGICAL SURVEY SECTION The Geological Survey Section shall, by law"...make such exami nation, survey, and mapping of the geology, mineralogy, and topo graphy of the state, including their industrial and economic utilization as it may consider necessary." In carrying out its duties under this law, the section promotes the wise conservation and use of mineral resources by industry, commerce, agriculture, and other governmental agencies for the general welfare of the citizens of North Carolina. The Section conducts a number of basic and applied research projects in environmental resource planning, mineral resource explora tion, mineral statistics, and systematic geologic mapping. Services constitute a major portion ofthe Sections's activities and include identi fying rock and mineral samples submitted by the citizens of the state and providing consulting services and specially prepared reports to other agencies that require geological information. The Geological Survey Section publishes results of research in a series of Bulletins, Economic Papers, Information Circulars, Educa tional Series, Geologic Maps, and Special Publications. -
New Mineral Names*,†
American Mineralogist, Volume 106, pages 1360–1364, 2021 New Mineral Names*,† Dmitriy I. Belakovskiy1, and Yulia Uvarova2 1Fersman Mineralogical Museum, Russian Academy of Sciences, Leninskiy Prospekt 18 korp. 2, Moscow 119071, Russia 2CSIRO Mineral Resources, ARRC, 26 Dick Perry Avenue, Kensington, Western Australia 6151, Australia In this issue This New Mineral Names has entries for 11 new species, including 7 minerals of jahnsite group: jahnsite- (NaMnMg), jahnsite-(NaMnMn), jahnsite-(CaMnZn), jahnsite-(MnMnFe), jahnsite-(MnMnMg), jahnsite- (MnMnZn), and whiteite-(MnMnMg); lasnierite, manganflurlite (with a new data for flurlite), tewite, and wumuite. Lasnierite* the LA-ICP-MS analysis, but their concentrations were below detec- B. Rondeau, B. Devouard, D. Jacob, P. Roussel, N. Stephant, C. Boulet, tion limits. The empirical formula is (Ca0.59Sr0.37)Ʃ0.96(Mg1.42Fe0.54)Ʃ1.96 V. Mollé, M. Corre, E. Fritsch, C. Ferraris, and G.C. Parodi (2019) Al0.87(P2.99Si0.01)Ʃ3.00(O11.41F0.59)Ʃ12 based on 12 (O+F) pfu. The strongest lines of the calculated powder X-ray diffraction pattern are [dcalc Å (I%calc; Lasnierite, (Ca,Sr)(Mg,Fe)2Al(PO4)3, a new phosphate accompany- ing lazulite from Mt. Ibity, Madagascar: an example of structural hkl)]: 4.421 (83; 040), 3.802 (63, 131), 3.706 (100; 022), 3.305 (99; 141), characterization from dynamic refinement of precession electron 2.890 (90; 211), 2.781 (69; 221), 2.772 (67; 061), 2.601 (97; 023). It diffraction data on submicrometer sample. European Journal of was not possible to perform powder nor single-crystal X-ray diffraction Mineralogy, 31(2), 379–388. -
The Seven Crystal Systems
Learning Series: Basic Rockhound Knowledge The Seven Crystal Systems The seven crystal systems are a method of classifying crystals according to their atomic lattice or structure. The atomic lattice is a three dimensional network of atoms that are arranged in a symmetrical pattern. The shape of the lattice determines not only which crystal system the stone belongs to, but all of its physical properties and appearance. In some crystal healing practices the axial symmetry of a crystal is believed to directly influence its metaphysical properties. For example crystals in the Cubic System are believed to be grounding, because the cube is a symbol of the element Earth. There are seven crystal systems or groups, each of which has a distinct atomic lattice. Here we have outlined the basic atomic structure of the seven systems, along with some common examples of each system. Cubic System Also known as the isometric system. All three axes are of equal length and intersect at right angles. Based on a square inner structure. Crystal shapes include: Cube (diamond, fluorite, pyrite) Octahedron (diamond, fluorite, magnetite) Rhombic dodecahedron (garnet, lapis lazuli rarely crystallises) Icosi-tetrahedron (pyrite, sphalerite) Hexacisochedron (pyrite) Common Cubic Crystals: Diamond Fluorite Garnet Spinel Gold Pyrite Silver Tetragonal System Two axes are of equal length and are in the same plane, the main axis is either longer or shorter, and all three intersect at right angles. Based on a rectangular inner structure. Crystal shapes include: Four-sided prisms and pyramids Trapezohedrons Eight-sided and double pyramids Icosi-tetrahedron (pyrite, sphalerite) Hexacisochedron (pyrite) Common Tetragonal Crystals: Anatase Apophyllite Chalcopyrite Rutile Scapolite Scheelite Wulfenite Zircon Hexagonal System Three out of the four axes are in one plane, of the same length, and intersect each other at angles of 60 degrees. -
Scandium Mineralization Associated with Hydrothermal Lazulite-Quartz Veins in the Lower Austroalpine Grobgneis Complex, Eastern Alps, Austria
Bernhard, F. (2001): Scandium mineralization associated with hydrothermal lazulite-quartz veins in the Lower Austroalpine Grobgneis complex, Eastern Alps, Austria. In: Piestrzynski A. et al. (eds.): Mineral Deposits at the Beginning of the 21st Century. Proceedings of the joint sixth biennial SGA-SEG meeting. Kraków, Poland. A.A.Balkema Publishers, 935-938. Scandium mineralization associated with hydrothermal lazulite-quartz veins in the Lower Austroalpine Grobgneis complex, Eastern Alps, Austria F. Bernhard Institut für Technische Geologie und Angewandte Mineralogie, Technische Universität Graz, Rechbauerstraße 12, A-8010 Graz, Austria ABSTRACT: Lazulite (MgAl2(PO4)2(OH)2)-quartz veins within the Lower Austroalpine Grobgneis complex, Austria, have Sc-contents up to 200 ppm. The predominant Sc-carrier is pretulite, ScPO4, and this phase oc- curs as a wide-spread accessory mineral. Vein formation took place at temperatures of 300-500° C and low pressure during Permo-Triassic extensional tectonics and fluid flow. Mg-enriched alteration zones suggest that vein material was not derived from the immediate host rocks. Eo-Alpine metamorphism and deformation overprinted the veins to varying degrees. Despite the low tonnage of the Sc-rich veins, this new type of Sc- mineralization may point to larger Sc-accumulations in similar phosphate-rich hydrothermal environments. 1 INTRODUCTION The long-known lazulite (MgAl2(PO4)2(OH)2)- quartz veins in northeastern Styria and southern Scandium is a moderately abundant transition ele- Lower Austria contain significant Sc-enrichments in ment with an average content ca. 7 ppm in the upper the form of pretulite, ScPO4 (Bernhard et al. 1998b). and ca. 25 ppm in the lower continental crust (We- This contribution gives data on the geology, miner- depohl 1995). -
Burangaite, a New Phosphate Mineral from Rwanda
BURANGAITE, A NEW PHOSPHATE MINERAL FROM RWANDA O. von KNORRING, MARTTI LEHTINEN and TH. G. SAHAMA KNORRING, O. von, LEHTINEN, MARTTI and SAHAMA, Th. G. 1977: Burangaite, a new phosphate mineral from Rwanda. BulL GeoL Soc. Finland 49: 33-36. This paper describes a new phosphate, burangaite, from the Buranga pegmatite in Rwanda. Burangaite is monoclinic with the idealized formula (Na,Ca)2 (Fe2+,Mg)2Aho(OH,Oh2(P04)S·4H20, Z = 2. The crystals exhibit narrow, bladed prisms, elongated parallel to the b-axis. Perfect cleavage parallel to 100. Mohs' hardness 5. Streak slightly bluish. 0 Unit-cell data: ao 25.09 A, bo 5.048 A, Co 13.45 A, fJ 110.91 , space group C2Ic. These parameters and the indexed X-ray powder pattern (Table 1) indicate a marked relationship with dufrenite. 0 The mineral is blue in color with y 11 band c /\a = 11 0, 2Va = 58 , strong pleochroism, refractive indices a 1.611, fJ 1.635, Y 1.643. Com mon hourglass structure with a blue core and a colorless margin. O. von Knorring, Department of Earth Sciences, Leeds University, Leeds LS2 9JT, England. Martti Lehtinen and Th. G. Sahama, Department of Geology and Mineralogy, University of Helsinki, P.O. Box 115, SF-00170 Hel sinki 17, Finland. Introduction commonly associated with bjarebyite (von Knorring and Fransolet 1975), wardite and The occurrence of a long-prismatic bluish other phosphates under study. Wardite occurs phosphate mineral from the Buranga pegma as white crystals of pyramidal habit, up to tite, Rwanda, was noted and provisionally 2 mm in size, with dominating {012} and described by one of us (von Knorring 1973). -
Compositional Asymmetry in Replacement Tourmaline – an Example from the Tauern Window, Eastern Alps
Geological Volume 4 Number 2 Mater ials August 12, 2002 Researc h Compositional asymmetry in replacement tourmaline – An example from the Tauern Window, Eastern Alps Darrell J. Henry1, Barbara L. Dutrow2 and Jane Selverstone3 1, 2Department of Geology and Geophysics, Louisiana State University, Baton Rouge, Louisiana 70808, USA 1<[email protected]>, 2<[email protected]>, 3Department of Earth and Planetary Sciences, University of New Mexico, Albuquerque, New Mexico 87131, USA 3<[email protected] > Abstract Tourmaline, partially replacing pre-existing tourmaline from a tectonically-dismembered tourmalinite vein, has developed distinctive compositional asymmetry that reflects influx of reac- tive fluids. The tourmalinite clast, enclosed in a quartzite from the Tauern Window, Eastern Alps, experienced a clockwise P-T-t path with maximal burial depths of 35-40 km (10-11 kbar), peak temperatures of ~550°C and major deformation preceding peak thermal conditions. The primary tourmaline of the tourmalinite clast, generation-1, is texturally and compositionally heterogeneous, ranging from schorl to dravite [Mg / (Mg + Fe) = 0.27 - 0.61] with highly-variable Al consistent X X with combinations of the Al(NaR)-1 and AlO(R(OH))-1 exchange vectors, where represents X-site vacancy and R is Fe2+ + Mn + Mg. Generation-2 tourmaline is manifest as distinctive compo- sitionally-asymmetric bands of colorless foitite (zone 1) and blue schorl (zone 2) replacing genera- tion-1 tourmaline. Replacement takes place along a scalloped margin and advances preferentially towards the analogous pole (-c) of generation-1 tourmaline. The two zones of generation-2 range from foitite to schorl with a restricted ratio of Mg / (Mg + Fe) of 0.32 - 0.41, but with variable X, X Al, Na and R predominantly reflecting Al(NaR)-1.