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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 -
Mineralogy and Geochemistry of Ocelli in the Damtjernite Dykes and Sills, Chadobets Uplift, Siberian Craton: Evidence of the Fluid–Lamprophyric Magma Interaction
minerals Article Mineralogy and Geochemistry of Ocelli in the Damtjernite Dykes and Sills, Chadobets Uplift, Siberian Craton: Evidence of the Fluid–Lamprophyric Magma Interaction Anna A. Nosova 1,*, Ludmila V. Sazonova 1,2, Alexey V. Kargin 1 , Elena O. Dubinina 1 and Elena A. Minervina 1 1 Institute of Geology of Ore Deposits, Petrography, Mineralogy and Geochemistry, Russian Academy of Sciences (IGEM RAS), 119017 Moscow, Russia; [email protected] (L.V.S.); [email protected] (A.V.K.); [email protected] (E.O.D.); [email protected] (E.A.M.) 2 Geology Department, Lomonosov Moscow State University, 119991 Moscow, Russia * Correspondence: [email protected]; Tel.:+7-499-230-8414 Abstract: The study reports petrography, mineralogy and carbonate geochemistry and stable iso- topy of various types of ocelli (silicate-carbonate globules) observed in the lamprophyres from the Chadobets Uplift, southwestern Siberian craton. The Chadobets lamprophyres are related to the REE-bearing Chuktukon carbonatites. On the basis of their morphology, mineralogy and relation with the surrounding groundmass, we distinguish three types of ocelli: carbonate-silicate, containing carbonate, scapolite, sodalite, potassium feldspar, albite, apatite and minor quartz ocelli (K-Na-CSO); carbonate–silicate ocelli, containing natrolite and sodalite (Na-CSO); and silicate-carbonate, con- taining potassium feldspar and phlogopite (K-SCO). The K-Na-CSO present in the most evolved Citation: Nosova, A.A.; Sazonova, damtjernite with irregular and polygonal patches was distributed within the groundmass; the patches L.V.; Kargin, A.V.; Dubinina, E.O.; consist of minerals identical to minerals in ocelli. Carbonate in the K-Na-CSO are calcite, Fe-dolomite Minervina, E.A. -
EVIDENCE for MAGMATIC-HYDROTHERMAL ACTIVITY on MARS from Cl-RICH SCAPOLITE in NAKHLA
45th Lunar and Planetary Science Conference (2014) 1620.pdf EVIDENCE FOR MAGMATIC-HYDROTHERMAL ACTIVITY ON MARS FROM Cl-RICH SCAPOLITE IN NAKHLA. J. Filiberto1, C.A. Goodrich2, A.H. Treiman3, J. Gross4, and P.A. Giesting1, 1Southern Illinois University, Geology Dept, Carbondale, IL 62901 USA, [email protected], 2Planetary Science Institute, Tucson AZ 85719 USA. 3Lunar and Planetary Institute, Houston, TX 77058 USA, 4American Museum of Natural History, New York, NY USA. Introduction: Scapolite is a common terrestrial The melt inclusion containing the Cl-scapolite (Fig. hydrothermal, metamorphic, and metasomatic mineral 1) is dominated by high-Ca pyroxene, K-feldspar and which forms by the reaction of plagioclase and a Cl- or K-rich glass, with minor chromite, Fe-sulfides, Fe-Ti CO2-rich fluid [1-3]. It is less common as a primary oxides, and alteration material [9]. The occurrence of igneous phase, but has been reported as megacrysts, the scapolite appears to be texturally equivalent to the phenocrysts, and oikocrysts in alkali-rich basaltic K-feldspar or the glass (i.e., interstitial to the pyrox- magmas [4-6]. Based on reflectance spectra, scapolite enes), and may therefore be replacing, or contempora- has also been suggested to exist on the surface of Mars neous with, one of these phases. It contains ~3.9 wt.% as a possible alteration mineral [7]. Cl, and has the formula (Na2.8Ca0.7K0.3)3.9(Si8.3Al3.7)12ClO24. Scapolite has three main end member composi- It is almost pure end-member marialite with little tions: marialite (Na4Al3Si9O24Cl), meionite meionite component (Fig. 2). -
Sulfate-Rich Scapolite on Mars?
Lunar and Planetary Science XXXVIII (2007) 1152.pdf Sulfate-rich Scapolite on Mars? J.J. Papike, J.M. Karner, and C.K. Shearer Astromaterials Institute, Department of Earth and Planetary Sciences, University of New Mexico, Albuquerque, New Mexico 87131 INTRODUCTION also shows selected bonds to neighboring Ca atoms. The surface of Mars shows abundant evidence for This configuration is remarkably stable in P-T space sulfur activity over a prolonged period in martian discussed below. history. Evidence goes back to the Viking landers in STABILITY 1976 but more recent orbital and landed in situ Figure 3 illustrates the stability field of SM [3]. The missions, including the two MER rovers, which are diagram shows that SM can be stable over the still active, confirm this. The identification of the pressure interval ~ 10 to 27 Kb at 1200 degrees C. sulfate jarosite with ferric iron confirms highly This corresponds to a depth interval of ~90 – 243 km oxidizing conditions near the martian surface. We depth in Mars (Fig. 4). In this depth range SM may speculate that conditions oxidizing enough to crystallize if the fO2 is high enough for S to exist as + crystallize a SO4 containing scapolite exist in the 6 . lower martian crust or upper mantle. This scapolite TERRESTRIAL OCCURENCES could be a important reservoir for sulfate in Mars and Terrestrial occurrences of igneous scapolite are might form either directly from sulfur-rich, oxidizing discussed in [2,4, and 5]. Boivin and Camus [4] magmas or by metasomatism of previously discuss a scapolite assemblage found as megacrysts crystallized plagioclase in basalt. -
Optical Properties of Common Rock-Forming Minerals
AppendixA __________ Optical Properties of Common Rock-Forming Minerals 325 Optical Properties of Common Rock-Forming Minerals J. B. Lyons, S. A. Morse, and R. E. Stoiber Distinguishing Characteristics Chemical XI. System and Indices Birefringence "Characteristically parallel, but Mineral Composition Best Cleavage Sign,2V and Relief and Color see Fig. 13-3. A. High Positive Relief Zircon ZrSiO. Tet. (+) 111=1.940 High biref. Small euhedral grains show (.055) parallel" extinction; may cause pleochroic haloes if enclosed in other minerals Sphene CaTiSiOs Mon. (110) (+) 30-50 13=1.895 High biref. Wedge-shaped grains; may (Titanite) to 1.935 (0.108-.135) show (110) cleavage or (100) Often or (221) parting; ZI\c=51 0; brownish in very high relief; r>v extreme. color CtJI\) 0) Gamet AsB2(SiO.la where Iso. High Grandite often Very pale pink commonest A = R2+ and B = RS + 1.7-1.9 weakly color; inclusions common. birefracting. Indices vary widely with composition. Crystals often euhedraL Uvarovite green, very rare. Staurolite H2FeAI.Si2O'2 Orth. (010) (+) 2V = 87 13=1.750 Low biref. Pleochroic colorless to golden (approximately) (.012) yellow; one good cleavage; twins cruciform or oblique; metamorphic. Olivine Series Mg2SiO. Orth. (+) 2V=85 13=1.651 High biref. Colorless (Fo) to yellow or pale to to (.035) brown (Fa); high relief. Fe2SiO. Orth. (-) 2V=47 13=1.865 High biref. Shagreen (mottled) surface; (.051) often cracked and altered to %II - serpentine. Poor (010) and (100) cleavages. Extinction par- ~ ~ alleL" l~4~ Tourmaline Na(Mg,Fe,Mn,Li,Alk Hex. (-) 111=1.636 Mod. biref. -
Metasomatic Alteration Associated with Regional Metamorphism: an Example from the Willyama Supergroup, South Australia
Lithos 54Ž. 2000 33±62 www.elsevier.nlrlocaterlithos Metasomatic alteration associated with regional metamorphism: an example from the Willyama Supergroup, South Australia A.J.R. Kent a,),1, P.M. Ashley a,2, C.M. Fanning b,3 a DiÕision of Earth Sciences, UniÕersity of New England, Armidale, NSW, 2351, Australia b Research School of Earth Sciences, The Australian National UniÕersity, Canberra, ACT, 0200, Australia Received 20 October 1998; accepted 12 May 2000 Abstract The Olary Domain, part of the Curnamona Province, a major Proterozoic terrane located within eastern South Australia and western New South Wales, Australia, is an excellent example of geological region that has been significantly altered by metasomatic mass-transfer processes associated with regional metamorphism. Examples of metasomatically altered rocks in the Olary Domain are ubiquitous and include garnet±epidote-rich alteration zones, clinopyroxene- and actinolite-matrix breccias, replacement ironstones and albite-rich alteration zones in quartzofeldspathic metasediments and intrusive rocks. Metasomatism is typically associated with formation of calcic, sodic andror iron-rich alteration zones and development of oxidised mineral assemblages containing one or more of the following: quartz, albite, actinolite±hornblende, andradite-rich garnet, epidote, magnetite, hematite and aegerine-bearing clinopyroxene. Detailed study of one widespread style of metasomatic alteration, garnet±epidote-rich alteration zones in calc-silicate host rocks, provides detailed information on the timing of metasomatism, the conditions under which alteration occurred, and the nature and origin of the metasomatic fluids. Garnet±epidote-bearing zones exhibit features such as breccias, veins, fracture-controlled alteration, open space fillings and massive replacement of pre-existing calc-silicate rock consistent with formation at locally high fluid pressures and fluidrrock ratios. -
Silvialite, a New Sulfate-Dominant Member of the Scapolite Group with an AI-Si Composition Near the 14/M-P42/N Phase Transition
Mineralogical Magazine, June 1999, Vol. 63(3), pp. 321-329 Silvialite, a new sulfate-dominant member of the scapolite group with an AI-Si composition near the 14/m-P42/n phase transition D. K. TEERTSTRA, M. SCHINDLER, B. L. SHERRIH AND F. C. HAWTHORNE Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba, Canada R3T 2N2 ABSTRACT Silvialite, i?eally Ca4A16Si6024S04, is tetragonal, 141m, Z = 2, with a = 12.160(3), c = 7.560(1) A, V= 1117.9(8) A3, c:a = 0.6217:1, co = 1.583, E = 1.558 (uniaxial negative), Dill = 2.75 g/cm3, Deale = 2.769 glcm.1 and H (Mohs) = 5.5. It is transparent and slightly yellow, has a good (100} cleavage, chonchoidal fracture, white streak and a vitreous lustre. It occurs in upper-mantle gamet-granulite xenoliths hosted by olivine nephelinite, from McBride Province, North Queensland, Australia. The empirical formula, derived from electron-microprobe analysis, is (NaI06Ca28(,)(AI4~7Si713)024 [(S04)OS7(C03)04IJ. Crystal-structure refinement shows disordered carbonate and sulfate groups along the fourfold axis. Silvialite is a primary cumulate phase precipitated from alkali basalt at 900- 1000'C and 8-12 kbar under high .Iso, and .I()" The name silvialite, currently used in literature to describe the sulfate analogue of meionite, was suggested by Brauns (1914). KEYWORDS:scapolite, meionite, silvialite, new mineral, sulfatc, X-ray data, electron-microprobe data, Queensland, Australia. Introduction Systematic Reference Series of the National Mineral Collection at the Geological Survey of MINERALSof the scapolite group have the general Canada, Ottawa, Ontario, under catalogue number formula M4TI202~, with M= Na, Ca, minor K; T NMC 68080. -
INVESTIGATION of a CAT's-EYE SCAPOLITE from SRI LANKA by K
INVESTIGATION OF A CAT'S-EYE SCAPOLITE FROM SRI LANKA By K. Schmetzer and H. Bank A cut gemstone with intense chatoyancy that Furthermore, hexagonal plates up to 0.4 x 0.4 originated from Sri Lanka was determined to be a mm in size with metallic luster were determined member of the scapolite solid-solution series, Indices to be pyrrhotite in these samples (Graziani and of refraction and unit-cell dimensions were found as Gubelin, 1981). w = 1.583, e = 1.553 and2 = 12.169, = 7.569 A, This article describes a scapolite crystal from respectively; a meionite content of 69% was Sri Lanlza that was cut into a 1.68-ct cabochon established by microprobe analysis. The chatoyancy (approximately 9 mm x 5 mm) with particularly is caused by needle-like inclusions with an orientation parallel to the c-axis of the scapolite host intense chatoyancy (figure 1). The ray of light crystal. Microprobe analysis of these needles showed crossing the surface of the cabochon is relatively them to be pyrrl~otite. broad compared to the sharpness of rays in other gemstones with chatoyancy or asterism, such as the more familiar cat's-eye chrysoberyls or aste- riated corundum. The physical and chemical properties of this cat's-eye scapolite are pre- Natural scapolites are members of the solid- sented, and the cause of the distinctive chatoy- solution series marialite, Nag[(C12,S04,C03)1 (A1 ancy in this stone is explained. Si308)e],and meionite, CadClaSO+C03) (A12 1 PHYSICAL AND CHEMICAL PROPERTIES Si20g)g].Scapolite crystals of gem quality occur colorless and in white, gray, yellow, pink, and A small facet was cut and polished on the bottom violet. -
Volume 23 / No. 7 / 1993
Volume 23 No. 7. July 1993 1116 Journal of Gemmology THE GEMMOLOGICAL ASSOCIATION AND GEM TESTING LABORATORY OF GREAT BRITAIN OFFICERS AND COUNCIL Past Presidents: Sir Henry Miers, MA, D.Sc., FRS Sir William Bragg, OM, KBE, FRS Dr. G.F. Herbert Smith, CBE, MA, D.Sc. Sir Lawrence Bragg, CH, OBE, MC, B.Sc, FRS Sir Frank Claringbull, Ph.D., F.Inst.P., FGS Vice-Presidents: R. K. Mitchell, FGA A.E. Farn, FGA D.G. Kent, FGA E. M. Bruton, FGA, DGA Council of Management CR. Cavey, FGA T.J. Davidson, FGA N.W. Deeks, FGA E.A. Jobbins, B.Sc, C.Eng., FIMM, FGA I. Thomson, FGA V.P. Watson, FGA, DGA R.R. Harding, B.Sc., D.Phil., FGA, C. Geol. Members' Council A. J. Allnutt, M.Sc, G.H. Jones, B.Sc, Ph.D., P. G. Read, C.Eng., Ph.D., FGA FGA MIEE, MIERE, FGA, DGA P. J. E. Daly, B.Sc, FGA J. Kessler I. Roberts, FGA P. Dwyer-Hickey, FGA, G. Monnickendam R. Shepherd DGA L. Music R. Velden R. Fuller, FGA, DGA J.B. Nelson, Ph.D., FGS, D. Warren B. Jackson, FGA F. Inst. P., C.Phys., FGA CH. Winter, FGA, DGA Branch Chairmen: Midlands Branch: D.M. Larcher, FBHI, FGA, DGA North-West Branch: I. Knight, FGA, DGA Examiners: A. J. Allnutt, M.Sc, Ph.D., FGA G. H. Jones, B.Sc, Ph.D., FGA L. Bartlett, B.Sc, M.Phil., FGA, DGA D. G. Kent, FGA E. M. Bruton, FGA, DGA R. D. Ross, B.Sc, FGA C R. -
Rubies and Sapphires from Snezhnoe, Tajikistan
FEATURE ARTICLES RUBIES AND SAPPHIRES FROM SNEZHNOE , T AJIKISTAN Elena S. Sorokina, Andrey K. Litvinenko, Wolfgang Hofmeister, Tobias Häger, Dorrit E. Jacob, and Zamoniddin Z. Nasriddinov Discovered during the late 1970s, the Snezhnoe ruby and sapphire deposit in Tajikistan was active until the collapse of the former Soviet Union in the early 1990s and the outbreak of regional conflicts. This marble-hosted occurrence has seen renewed interest, as it is a large and potentially productive deposit that has not been sufficiently studied. Testing of samples identified solid inclusions of margarite enriched with Na and Li (calcic ephesite or soda margarite). These are believed to be previously unreported for gem corundum. Allanite, muscovite, and fuchsite (chromium-bearing muscovite) were identified for the first time in ruby and sapphire from Snezhnoe. These and other inclusions such as zircon, rutile, K- feldspar, and Ca-Na-plagioclase could serve to distinguish them from stones mined elsewhere. Con - centrations of trace elements were typical for ruby and sapphire of the same formation type. The highest Cr concentrations were observed within the bright red marble-hosted rubies, and these values were very similar to those of the famous Burmese rubies from Mogok. orundum— -Al O —is a common, though net, scapolite, lazurite, and variscite (Litvinenko α 2 3 minor, component of many metamorphic and Barnov, 2010). The occurrence of ruby in the Crocks. Gem-quality varieties of ruby and sap - Pamirs was first suggested by the Soviet mineralo - phire occur in only a few primary metamorphic and magmatic rock types depleted in silica and enriched Figure 1. -
Minerals Found in Michigan Listed by County
Michigan Minerals Listed by Mineral Name Based on MI DEQ GSD Bulletin 6 “Mineralogy of Michigan” Actinolite, Dickinson, Gogebic, Gratiot, and Anthonyite, Houghton County Marquette counties Anthophyllite, Dickinson, and Marquette counties Aegirinaugite, Marquette County Antigorite, Dickinson, and Marquette counties Aegirine, Marquette County Apatite, Baraga, Dickinson, Houghton, Iron, Albite, Dickinson, Gratiot, Houghton, Keweenaw, Kalkaska, Keweenaw, Marquette, and Monroe and Marquette counties counties Algodonite, Baraga, Houghton, Keweenaw, and Aphrosiderite, Gogebic, Iron, and Marquette Ontonagon counties counties Allanite, Gogebic, Iron, and Marquette counties Apophyllite, Houghton, and Keweenaw counties Almandite, Dickinson, Keweenaw, and Marquette Aragonite, Gogebic, Iron, Jackson, Marquette, and counties Monroe counties Alunite, Iron County Arsenopyrite, Marquette, and Menominee counties Analcite, Houghton, Keweenaw, and Ontonagon counties Atacamite, Houghton, Keweenaw, and Ontonagon counties Anatase, Gratiot, Houghton, Keweenaw, Marquette, and Ontonagon counties Augite, Dickinson, Genesee, Gratiot, Houghton, Iron, Keweenaw, Marquette, and Ontonagon counties Andalusite, Iron, and Marquette counties Awarurite, Marquette County Andesine, Keweenaw County Axinite, Gogebic, and Marquette counties Andradite, Dickinson County Azurite, Dickinson, Keweenaw, Marquette, and Anglesite, Marquette County Ontonagon counties Anhydrite, Bay, Berrien, Gratiot, Houghton, Babingtonite, Keweenaw County Isabella, Kalamazoo, Kent, Keweenaw, Macomb, Manistee, -
Identification Tables for Common Minerals in Thin Section
Identification Tables for Common Minerals in Thin Section These tables provide a concise summary of the properties of a range of common minerals. Within the tables, minerals are arranged by colour so as to help with identification. If a mineral commonly has a range of colours, it will appear once for each colour. To identify an unknown mineral, start by answering the following questions: (1) What colour is the mineral? (2) What is the relief of the mineral? (3) Do you think you are looking at an igneous, metamorphic or sedimentary rock? Go to the chart, and scan the properties. Within each colour group, minerals are arranged in order of increasing refractive index (which more or less corresponds to relief). This should at once limit you to only a few minerals. By looking at the chart, see which properties might help you distinguish between the possibilities. Then, look at the mineral again, and check these further details. Notes: (i) Name: names listed here may be strict mineral names (e.g., andalusite), or group names (e.g., chlorite), or distinctive variety names (e.g., titanian augite). These tables contain a personal selection of some of the more common minerals. Remember that there are nearly 4000 minerals, although 95% of these are rare or very rare. The minerals in here probably make up 95% of medium and coarse-grained rocks in the crust. (ii) IMS: this gives a simple assessment of whether the mineral is common in igneous (I), metamorphic (M) or sedimentary (S) rocks. These are not infallible guides - in particular many igneous and metamorphic minerals can occur occasionally in sediments.