PRELIMINARY EVALUATION of BEDROCK POTENTIAL for NATURALLY OCCURRING ASBESTOS in ALASKA by Diana N
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Podiform Chromite Deposits—Database and Grade and Tonnage Models
Podiform Chromite Deposits—Database and Grade and Tonnage Models Scientific Investigations Report 2012–5157 U.S. Department of the Interior U.S. Geological Survey COVER View of the abandoned Chrome Concentrating Company mill, opened in 1917, near the No. 5 chromite mine in Del Puerto Canyon, Stanislaus County, California (USGS photograph by Dan Mosier, 1972). Insets show (upper right) specimen of massive chromite ore from the Pillikin mine, El Dorado County, California, and (lower left) specimen showing disseminated layers of chromite in dunite from the No. 5 mine, Stanislaus County, California (USGS photographs by Dan Mosier, 2012). Podiform Chromite Deposits—Database and Grade and Tonnage Models By Dan L. Mosier, Donald A. Singer, Barry C. Moring, and John P. Galloway Scientific Investigations Report 2012-5157 U.S. Department of the Interior U.S. Geological Survey U.S. Department of the Interior KEN SALAZAR, Secretary U.S. Geological Survey Marcia K. McNutt, Director U.S. Geological Survey, Reston, Virginia: 2012 This report and any updates to it are available online at: http://pubs.usgs.gov/sir/2012/5157/ For more information on the USGS—the Federal source for science about the Earth, its natural and living resources, natural hazards, and the environment—visit http://www.usgs.gov or call 1–888–ASK–USGS For an overview of USGS information products, including maps, imagery, and publications, visit http://www.usgs.gov/pubprod To order this and other USGS information products, visit http://store.usgs.gov Suggested citation: Mosier, D.L., Singer, D.A., Moring, B.C., and Galloway, J.P., 2012, Podiform chromite deposits—database and grade and tonnage models: U.S. -
Current Best Practices for Vermiculite Attic Insulation
What is vermiculite insulation? What if I occasionally have to go into Vermiculite is a naturally occurring mineral that has my attic? the unusual property of expanding into worm-like EPA and ATSDR strongly recommend that accordion shaped pieces when heated. The homeowners make every effort not to disturb expanded vermiculite is a light-weight, fire- vermiculite insulation in their attics. If you resistant, absorbent, and odorless material. These occasionally have to go into your attic, current best properties allow vermiculite to be used to make practices state you should: numerous products, including attic insulation. 1. Make every effort to stay on the floored part Do I have vermiculite insulation? of your attic and to not disturb the Vermiculite can be purchased in various forms for insulation. various uses. Sizes of vermiculite products range 2. If you must perform activities that may from very fine particles to large (coarse) pieces disturb the attic insulation such as moving nearly an inch long. Vermiculite attic insulation is a boxes (or other materials), do so as gently pebble-like, pour-in product and is usually light- as possible to minimize the disturbance. brown or gold in color. The pictures in the center of What should I do if I have 3. Leave the attic immediately after the this pamphlet and on the cover show several disturbance. samples of vermiculite attic insulation. vermiculite attic insulation? 4. If you need work done in your attic such as DO NOT DISTURB IT. Any disturbance has the the installation of cable or utility lines, hire trained and certified professionals who can Is vermiculite insulation a problem? potential to release asbestos fibers into the air. -
Greensand.Pdf
www.natureswayresources.com GREENSAND Greensand is a naturallyoccurring mineral mined from ocean deposits from a sedimentary rock known as “Glauconite”. It is often an olive-green colored sandstonerock found in layers in many sedimentary rock formations. Origin of Greensand Greensand forms in anoxic (without oxygen) marine environments that are rich in organic detritus and low in sedimentary inputs. Some greensands contain marine fossils (i.e. New Jersey Greensand). Greensand has been found in deposits all over the world. The greenish color comes from the mineral glauconite and iron potassiumsilicate that weathers and breaks down releasing the stored minerals. The color may range from a dark greenish gray, green-black to blue-green dependingon the minerals and water content. It often weatherseasilyand forms nodules that have been oxidized with iron bearing minerals that has a reddish brown or rust color. +3 The major chemical description is ((K,Na)(Fe , Al, Mg)2(Si,Al)4O10(OH)2) General chemical information: Iron (Fe) 12-19% Potassium (K) 5-7 % Silicon (Si) 25.0% Oxygen (O) 45% Magnesium (Mg) 2-3 % Aluminum (Al) 1.9 % Sodium (Na) 0.27% Hydrogen (H) 0.47% Over 30 other trace minerals and many micronutrients. Types of Greensand Glauconite is the namegiven to a group of naturally occurring iron rich silica minerals that may be composed of pellets or grains. When glauconite is mined the upper layers that have weathered and become oxidizedand minerals are released.These sometimes form pyrite a iron sulfide (FeS2) when oxygen is www.natureswayresources.com absent. In the deeper layers or reduced zone pyrite crystals often form. -
Module 7 Igneous Rocks IGNEOUS ROCKS
Module 7 Igneous Rocks IGNEOUS ROCKS ▪ Igneous Rocks form by crystallization of molten rock material IGNEOUS ROCKS ▪ Igneous Rocks form by crystallization of molten rock material ▪ Molten rock material below Earth’s surface is called magma ▪ Molten rock material erupted above Earth’s surface is called lava ▪ The name changes because the composition of the molten material changes as it is erupted due to escape of volatile gases Rocks Cycle Consolidation Crystallization Rock Forming Minerals 1200ºC Olivine High Ca-rich Pyroxene Ca-Na-rich Amphibole Intermediate Na-Ca-rich Continuous branch Continuous Discontinuous branch Discontinuous Biotite Na-rich Plagioclase feldspar of liquid increases liquid of 2 Temperature decreases Temperature SiO Low K-feldspar Muscovite Quartz 700ºC BOWEN’S REACTION SERIES Rock Forming Minerals Olivine Ca-rich Pyroxene Ca-Na-rich Amphibole Na-Ca-rich Continuous branch Continuous Discontinuous branch Discontinuous Biotite Na-rich Plagioclase feldspar K-feldspar Muscovite Quartz BOWEN’S REACTION SERIES Rock Forming Minerals High Temperature Mineral Suite Olivine • Isolated Tetrahedra Structure • Iron, magnesium, silicon, oxygen • Bowen’s Discontinuous Series Augite • Single Chain Structure (Pyroxene) • Iron, magnesium, calcium, silicon, aluminium, oxygen • Bowen’s Discontinuos Series Calcium Feldspar • Framework Silicate Structure (Plagioclase) • Calcium, silicon, aluminium, oxygen • Bowen’s Continuous Series Rock Forming Minerals Intermediate Temperature Mineral Suite Hornblende • Double Chain Structure (Amphibole) -
Mid-Infrared Optical Constants of Clinopyroxene and Orthoclase Derived from Oriented Single-Crystal Reflectance Spectra
American Mineralogist, Volume 99, pages 1942–1955, 2014 Mid-infrared optical constants of clinopyroxene and orthoclase derived from oriented single-crystal reflectance spectra JESSICA A. ARNOLD1,*, TIMOTHY D. GLOTCH1 AND ANNA M. PLONKA1 1Department of Geosciences, Stony Brook University, Stony Brook, New York 11794, U.S.A. ABSTRACT We have determined the mid-IR optical constants of one alkali feldspar and four pyroxene compo- sitions in the range of 250–4000 cm–1. Measured reflectance spectra of oriented single crystals were iteratively fit to modeled spectra derived from classical dispersion analysis. We present the real and imaginary indices of refraction (n and k) along with the oscillator parameters with which they were modeled. While materials of orthorhombic symmetry and higher are well covered by the current literature, optical constants have been derived for only a handful of geologically relevant monoclinic materials, including gypsum and orthoclase. Two input parameters that go into radiative transfer models, the scattering phase function and the single scattering albedo, are functions of a material’s optical constants. Pyroxene is a common rock-forming mineral group in terrestrial bodies as well as meteorites and is also detected in cosmic dust. Hence, having a set of pyroxene optical constants will provide additional details about the composition of Solar System bodies and circumstellar materials. We follow the method of Mayerhöfer et al. (2010), which is based on the Berreman 4 × 4 matrix formulation. This approach provides a consistent way to calculate the reflectance coefficients in low- symmetry cases. Additionally, while many models assume normal incidence to simplify the dispersion relations, this more general model applies to reflectance spectra collected at non-normal incidence. -
Nature of Interlayer Material in Silicate Clays of Selected Oregon Soils
AN ABSTRACT OF THE THESIS OF PAUL C, SINGLETON for the Ph.D. in Soils (Name) (Degree) (Major) Date thesis is presented July 28, 1965 Title NATURE OF INTERLAYER MATERIAL IN SILICATE CLAYS OF SELECTED OREGON SOILS - Redacted for Privacy Abstract approved = ajor professor) Ç A study was conducted to investigate the nature of hydroxy interlayers in the chlorite -like intergrade clays of three Oregon soils with respect to kind, amount, stability, and conditions of formation. The clays of the Hembre, Wren, and Lookout soils, selected to represent weathering products originating from basaltic materials under humid, subhumid, and semi -arid climatic conditions respectively, were subjected to a series of progressive treatments designed to effect a differential dissolution of the materials intimately asso- ciated with them. The treatments, chosen to represent a range of increasing severity of dissolution, were (1) distilled water plus mechanical stirring, (2) boiling 2% sodium carbonate, (3) buffered sodium citrate -dithionite, (4) boiling sodium hydroxide, and (5) preheating to 400 °C for 4 hours plus boiling sodium hydroxide. Extracts from the various steps of the dissolution procedure were chemically analyzed in order to identify the materials removed from the clays. X -ray diffraction analysis and cation exchange capacity determinations were made on the clays after each step, and any differences noted in the measured values were attributed to the removal of hydroxy interlayers from the clays. Hydroxy interlayers were found to occur more in the Hembre and Wren soils than in the Lookout soil, with the most stable interlayers occurring in the Wren. Soil reaction was one of the major differences between these soils. -
Clay Minerals Soils to Engineering Technology to Cat Litter
Clay Minerals Soils to Engineering Technology to Cat Litter USC Mineralogy Geol 215a (Anderson) Clay Minerals Clay minerals likely are the most utilized minerals … not just as the soils that grow plants for foods and garment, but a great range of applications, including oil absorbants, iron casting, animal feeds, pottery, china, pharmaceuticals, drilling fluids, waste water treatment, food preparation, paint, and … yes, cat litter! Bentonite workings, WY Clay Minerals There are three main groups of clay minerals: Kaolinite - also includes dickite and nacrite; formed by the decomposition of orthoclase feldspar (e.g. in granite); kaolin is the principal constituent in china clay. Illite - also includes glauconite (a green clay sand) and are the commonest clay minerals; formed by the decomposition of some micas and feldspars; predominant in marine clays and shales. Smectites or montmorillonites - also includes bentonite and vermiculite; formed by the alteration of mafic igneous rocks rich in Ca and Mg; weak linkage by cations (e.g. Na+, Ca++) results in high swelling/shrinking potential Clay Minerals are Phyllosilicates All have layers of Si tetrahedra SEM view of clay and layers of Al, Fe, Mg octahedra, similar to gibbsite or brucite Clay Minerals The kaolinite clays are 1:1 phyllosilicates The montmorillonite and illite clays are 2:1 phyllosilicates 1:1 and 2:1 Clay Minerals Marine Clays Clays mostly form on land but are often transported to the oceans, covering vast regions. Kaolinite Al2Si2O5(OH)2 Kaolinite clays have long been used in the ceramic industry, especially in fine porcelains, because they can be easily molded, have a fine texture, and are white when fired. -
VERMICULITE by Michael J
VERMICULITE By Michael J. Potter Domestic survey data and tables were prepared by Nicholas Muniz, statistical assistant, and the world production table was prepared by Glenn J. Wallace, international data coordinator. +2 Vermiculite is a hydrated magnesium-aluminum-iron silicate, with a suggested formula of (Mg,Fe ,Al)3(Al,Si)4O10(OH)2·4H2O (Fleisher and Mandarino, 1991, p. 211). Flakes of raw vermiculite concentrate are mica-like in appearance and contain water molecules within their internal structure. When the flakes are heated rapidly at a temperature of 900º C or higher, the water flashes into steam, and the flakes expand into accordion-like particles. The color, which can range from black and various shades of brown to yellow for the raw flakes, changes upon expansion to gold or bronze. This expansion process is called exfoliation, and the resulting lightweight material is chemically inert, fire resistant, and odorless. In lightweight plaster and concrete, vermiculite provides good thermal insulation. Vermiculite can absorb such liquids as fertilizers, herbicides, and insecticides, which can then be transported as free-flowing solids (Harben and Kuzvart, 1996). Production Domestic production (sold or used) data for vermiculite were collected by the U.S. Geological Survey (USGS) from two voluntary canvasses—one for mine-mill (concentrator) operations and the other for exfoliation plants. Data were not available for the three mine-mill operations. The two U.S. producers of vermiculite concentrate were Virginia Vermiculite Ltd. with operations near Woodruff, SC, and in Louisa County, VA; and W.R. Grace & Co. from its operation at Enoree, SC. Vermiculite concentrate was shipped to exfoliating plants for conversion into lightweight material. -
Geochemistry of an Ultramafic-Rodingite Rock Association in the Paleoproterozoic Dixcove Greenstone Belt, Southwestern Ghana
Journal of African Earth Sciences 45 (2006) 333–346 www.elsevier.com/locate/jafrearsci Geochemistry of an ultramafic-rodingite rock association in the Paleoproterozoic Dixcove greenstone belt, southwestern Ghana Kodjopa Attoh a,*, Matthew J. Evans a,1, M.E. Bickford b a Department of Earth and Atmospheric Sciences, Cornell University, Snee Hall, Ithaca, NY 14853, USA b Department of Earth Sciences, Syracuse University, Syracuse, NY 13244, USA Received 11 January 2005; received in revised form 20 February 2006; accepted 2 March 2006 Available online 18 May 2006 Abstract Rodingite occurs in ultramafic rocks within the Paleoproterozoic (Birimian) Dixcove greenstone belt in southwestern Ghana. U–Pb analyses of zircons from granitoids intrusive into the greenstone belt constrain the age of the rodingite-ultramafic association to be older than 2159 Ma. The ultramafic complex consists of variably serpentinized dunite and harzburgite overlain by gabbroic rocks, which together show petrographic and geochemical characteristics consistent with their formation by fractional crystallization involving olivine and plagioclase cumulates. Major and trace element concentrations and patterns in the ultramafic–mafic cumulate rocks and associated plagiogranite are similar to rocks in ophiolitic suites. The rodingites, which occur as irregular pods and lenses, and as veins and blocks in the serpentinized zones, are characterized by high Al2O3 and CaO contents, which together with petrographic evidence indicate their formation from plagioclase-rich protoliths. The peridotites are highly depleted in REE and display flat, chondrite-normalized REE pat- terns with variable, but mostly small, positive Eu anomalies whereas the rodingites, which are also highly depleted, with overall REE contents from 0.04 to 1.2 times chondrite values, display distinct large positive Eu anomalies. -
Metamorphism
Title page INTRODUCING METAMORPHISM Ian Sanders DUNEDIN EDINBURGH LONDON Contents Contents v Preface ix Acknowledgements x 1 Introduction 1 1.1 What is metamorphism? 1 1.1.1 Protoliths 1 1.1.2 Changes to the minerals 1 1.1.3 Changes to the texture 3 1.1.4 Naming metamorphic rocks 3 1.2 Metamorphic rocks – made under mountains 3 1.2.1 Mountain building 3 1.2.2 Directed stress, pressure and temperature in a mountain’s roots 4 1.2.3 Exhumation of a mountain’s roots 6 1.3 Metamorphism in local settings 6 1.3.1 Contact metamorphism 7 1.3.2 Hydrothermal metamorphism 7 1.3.3 Dynamic metamorphism 9 1.3.4 Shock metamorphism 9 2 The petrography of metamorphic rocks 11 2.1 Quartzite and metapsammite 11 2.1.1 Quartzite 11 2.1.2 Metapsammite 13 2.2 Metapelite 13 2.2.1 Slate 14 2.2.2 Phyllite and low-grade schist 16 2.2.3 Minerals and textures of medium-grade schist 17 2.2.4 The regional distribution of minerals in low- and medium-grade schist 20 2.2.5 Pelitic gneiss and migmatite 22 2.2.6 Metapelite in a contact aureole 23 2.2.7 The significance of Al2SiO5 for inferring metamorphic conditions 23 2.3 Marble 24 2.3.1 Pure calcite marble 24 2.3.2 Impure marble 26 2.3.3 Metasediments with mixed compositions 29 CONTENTS 2.4 Metabasite 30 2.4.1 Six kinds of metabasite from regional metamorphic belts 31 2.4.2 The ACF triangle for minerals in metabasites 36 2.4.3 P–T stability of metabasites, and metamorphic facies 38 vi 2.4.4 A metabasite made by contact metamorphism 40 2.5 Metagranite 41 2.5.1 Granitic gneiss and orthogneiss 41 2.5.2 Dynamic metamorphism -
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. -
Sulfide Mineralization in an Ultramafic-Rock Hosted Seafloor
Marine Geology 245 (2007) 20–39 www.elsevier.com/locate/margeo Sulfide mineralization in an ultramafic-rock hosted seafloor hydrothermal system: From serpentinization to the formation of Cu–Zn–(Co)-rich massive sulfides ⁎ Ana Filipa A. Marques a,b, , Fernando J.A.S. Barriga a, Steven D. Scott b a CREMINER (LA/ISR), Universidade de Lisboa, Faculdade de Ciências, Departamento de Geologia, Edif. C6 Piso 4. 1749-016 Campo Grande, Lisboa, Portugal b Scotiabank Marine Geology Research Laboratory, Department of Geology, University of Toronto, 22 Russell St., Toronto, Canada M5S 3B1 Received 12 December 2006; received in revised form 2 May 2007; accepted 12 May 2007 Abstract The Rainbow vent field is an ultramafic rock-hosted seafloor hydrothermal system located on the Mid-Atlantic ridge issuing high temperature, acidic, metal-rich fluids. Hydrothermal products include Cu–Zn–(Co)-rich massive sulfides with characteristics comparable to those found in mafic volcanic-hosted massive sulfide deposits. Petrography, mineralogy and geochemistry of nonmineralized and mineralized rocks sampled in the Rainbow vent field indicate that serpentinized peridotites host the hydrothermal vent system but serpentinization reactions occurred prior to and independently of the sulfide mineralization event. The onset of sulfide mineralization is reflected by extensive textural and chemical transformations in the serpentine-group minerals that show clear signs of hydrothermal corrosion. Element remobilization is a recurrent process in the Rainbow vent field rocks and, during simple peridotite serpentinization, Ni and Cr present in olivine and pyroxene are incorporated in the pseudomorphic serpentine mesh and bastite, respectively. Ni is later remobilized from pseudomorphic serpentine into the newly formed sulfides as a result of extensive hydrothermal alteration.