Phyllosilicates – (Silicate Sheets)
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17. Clay Mineralogy of Deep-Sea Sediments in the Northwestern Pacific, Dsdp, Leg 20
17. CLAY MINERALOGY OF DEEP-SEA SEDIMENTS IN THE NORTHWESTERN PACIFIC, DSDP, LEG 20 Hakuyu Okada and Katsutoshi Tomita, Department of Geology, Kagoshima University, Kagoshima 890, Japan INTRODUCTION intensity of montmorillonite can be obtained by sub- tracting the (001) reflection intensity of chlorite from the Clay mineral study of samples collected during Leg 20 of preheating or pretreating reflection intensity at 15 Å. the Deep Sea Drilling Project in the western north Pacific In a specimen with coexisting kaolinite and chlorite, was carried out mainly by means of X-ray diffraction their overlapping reflections make it difficult to determine analyses. Emphasis was placed on determining vertical quantitatively these mineral compositions. For such speci- changes in mineral composition of sediments at each site. mens Wada's method (Wada, 1961) and heat treatment Results of the semiquantitative and quantitative deter- were adopted. minations of mineral compositions of analyzed samples are The following shows examples of the determination of shown in Tables 1, 2, 3, 5, and 7. The mineral suites some intensity ratios of reflections of clay minerals. presented here show some unusual characters as discussed below. The influence of burial diagenesis is also evidenced Case 1 in the vertical distribution of some authigenic minerals. Montmorillonite (two layers of water molecules between These results may contribute to a better understanding silicate layers)—kaolinite mixture. of deep-sea sedimentation on the northwestern Pacific This is the situation in which samples contain both plate. montmorillonite and kaolinite. The first-order basal reflec- tions of these minerals do not overlap. When the (002) ANALYTICAL PROCEDURES reflection of montmorillonite, which appears at about 7 Å, Each sample was dried in air, and X-ray diffraction is absent or negligible, the intensity ratio is easily obtained. -
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. -
A Ground Magnetic Survey of Kimberlite Intrusives in Elliott County, Kentucky
Kentucky Geological Survey James C. Cobb, State Geologist and Director University of Kentucky, Lexington A Ground Magnetic Survey of Kimberlite Intrusives in Elliott County, Kentucky John D. Calandra Thesis Series 2 Series XII, 2000 Kentucky Geological Survey James C. Cobb, State Geologist and Director University of Kentucky, Lexington A Ground Magnetic Survey of Kimberlite Intrusives in Elliott County, Kentucky John D. Calandra On the cover: Photomicrographs of olivine phenoc- rysts: (top) a stressed first-generation olivine pheno- cryst and (bottom) a late-stage olivine phenocryst. Thesis Series 2 Series XII, 2000 i UNIVERSITY OF KENTUCKY Computer and Laboratory Services Section: Charles T. Wethington Jr., President Steven Cordiviola, Head Fitzgerald Bramwell, Vice President for Research and Richard E. Sergeant, Geologist IV Graduate Studies Joseph B. Dixon, Information Technology Manager I Jack Supplee, Director, Administrative Affairs, Research James M. McElhone, Information Systems Technical and Graduate Studies Support Specialist IV Henry E. Francis, Scientist II KENTUCKY GEOLOGICAL SURVEY ADVISORY Karen Cisler, Scientist I BOARD Jason S. Backus, Research Analyst Henry M. Morgan, Chair, Utica Steven R. Mock, Research Analyst Ron D. Gilkerson, Vice Chair, Lexington Tracy Sizemore, Research Analyst William W. Bowdy, Fort Thomas Steve Cawood, Frankfort GEOLOGICAL DIVISION Hugh B. Gabbard, Winchester Coal and Minerals Section: Kenneth Gibson, Madisonville Donald R. Chesnut Jr., Head Mark E. Gormley, Versailles Garland R. Dever Jr., Geologist V Rosanne Kruzich, Louisville Cortland F. Eble, Geologist V W.A. Mossbarger, Lexington Gerald A. Weisenfluh, Geologist V Jacqueline Swigart, Louisville David A. Williams, Geologist V, Henderson office John F. Tate, Bonnyman Stephen F. Greb, Geologist IV David A. -
PARAGONITE PSEUDOMORPHS AFTER KYANITE from TURKEY HEAVEN MOUNTAIN, CLEBURNE COUNTY, ALABAMA1 Tnonnron L. Noarnnnu, Geological Su
THE AMERICAN MINERALOGIST, VOL, 50, MAY_JIJ'}IE, 1965 PARAGONITE PSEUDOMORPHS AFTER KYANITE FROM TURKEY HEAVEN MOUNTAIN, CLEBURNE COUNTY, ALABAMA1 TnonNroN L. Noarnnnu, GeologicalSuraey of Alabama, Uniaersity, Alabama. ABSTRACT Paragonite pseudomorphs after kyanite have been found in the Turkey Heaven Moun- tain kyanite prospects. The pseudomorphs range in size from microscopic grains to mega- scopic prisms, which resemble andalusite crystals Optical, o-ray and petrographic studies indicate direct hysterogenic paragonite alteration of the kyanite. INrnolucrroN An investigationof kyanite prospectsin Sections22 and29,T.17 5., R. 11 E., at Turkey Heaven Mountain, Cleburne County, Alabama, discloseda unique mineral occurrence.The mineral assemblageincludes hysterogenicparagonite pseudomorphsafter kyanite, which resemble andalusite.The geneticphysicochemical parameters are consideredas a function of retrogrademetamorphism within a restrictive water environ- ment. GBor-ocrc SB:rrrNc The Turkey Heaven Mountain areais underlain by two metamorphic rock units: 1) the WedoweeFormation, a highly resistantgraphite-mica schist,and 2) a unit of the Ashland Mica Schist,an extensivelyweathered garnet-muscovite schist. Fresh rock exposuresindicate a retrograde metamorphic cycle from an almandine-amphibolite facies to a green- schist facies. At the crest of Turkey Heaven Mountain, the Wedowee Formation over-liesthe Ashland Mica Schist.The resistantgraphite-mica schist of the WedoweeFormation and associatedquartz veins contribute to the physiographic configuration of the area. The generalregional strike in the Alabama crystalline belt is about N. 45o E., and the dip is generally southeast.The crystalline area has undergoneprimary deformationfrom the stressesapplied generallyfrom the southeast,which producedisoclinal folding and thrust faulting to the northwest. Geologic studies at Turkey Heaven Mountain indicate a secondperiod of deformation in which the stressdirection can be ex- pressedaS a northeast shear couple that formed nonplanar, non-cylin- drical left lateral drag folds. -
Chemical and Structural Evolution of “Metamorphic Vermiculite” in Metaclastic Rocks of the Betic Cordillera, Málaga, Spain: a Synthesis
249 The Canadian Mineralogist Vol. 44, pp. 249-265 (2006) CHEMICAL AND STRUCTURAL EVOLUTION OF “METAMORPHIC VERMICULITE” IN METACLASTIC ROCKS OF THE BETIC CORDILLERA, MÁLAGA, SPAIN: A SYNTHESIS MARÍA DOLORES RUIZ CRUZ§ Departamento de Química Inorgánica, Cristalografía y Mineralogía, Universidad de Málaga, Campus de Teatinos, E-29071 Málaga, Spain JOSÉ MIGUEL NIETO Departamento de Geología, Facultad de Ciencias Experimentales, Universidad de Huelva, E-21071 Huelva, Spain ABSTRACT Vermiculite-like minerals from a metamorphic sequence of the Betic Cordillera, near Málaga, southeastern Spain, were investigated in detail by X-ray diffraction, electron-microprobe analysis, and transmission-analytical electron microscopy. Our results reveal that the chlorite-to-biotite transformation is much more complex than previously assumed. In addition to mixed- layer minerals with a mica:chlorite ratio of 2:1 and 1:1, which had previously been identifi ed, mixed-layer phases with very high and very low chlorite:vermiculite ratios have been identifi ed, together with true vermiculite, as intermediate steps in the chlorite-to-biotite transformation. The observed sequence is: chlorite → random to ordered 1:2 mica–chlorite mixed-layer phases → regular 1:1 chlorite–vermiculite mixed-layer phases → Vrm-rich chlorite–vermiculite mixed-layer phases → vermiculite → biotite. This sequence includes a continuous increase of interlayer cation content, and is similar to that described in the smectite- to-illite transformation. The high Na content of most of these phases suggests that in the absence of K-feldspar, two parallel sites of reactants, chlorite + phengite and chlorite + albite, account for the formation of vermiculitic phases, and later, of biotite. Keywords: mixed-layer minerals, metamorphic vermiculite, X-ray diffraction, electron-microprobe analysis, transmission elec- tron microscopy, analytical electron microscopy, Betic Cordillera, Spain. -
Mineralogy, Fluid Inclusion, and Stable Isotope Studies of the Hog Heaven Mining District, Flathead County, Montana
Montana Tech Library Digital Commons @ Montana Tech Graduate Theses & Non-Theses Student Scholarship Spring 2020 MINERALOGY, FLUID INCLUSION, AND STABLE ISOTOPE STUDIES OF THE HOG HEAVEN MINING DISTRICT, FLATHEAD COUNTY, MONTANA Ian Kallio Follow this and additional works at: https://digitalcommons.mtech.edu/grad_rsch Part of the Geological Engineering Commons MINERALOGY, FLUID INCLUSION, AND STABLE ISOTOPE STUDIES OF THE HOG HEAVEN MINING DISTRICT, FLATHEAD COUNTY, MONTANA by Ian Kallio A thesis submitted in partial fulfillment of the requirements for the degree of Masters of Science in Geoscience Geology Option Montana Tech 2020 ii Abstract The Hog Heaven mining district in northwestern Montana is unique in that it is a high- sulfidation epithermal system containing high Ag-Pb-Zn relative to Au-Cu, with a very high Ag to Au ratio (2,330:1). The deposits are hosted within the Cenozoic Hog Heaven volcanic field (HHVF), a 30 to 36 Ma suite that consists predominantly of rhyodacite flow-dome complexes and pyroclastic rocks. The HHVF is underlain by shallow-dipping siliclastic sediments of the Mesoproterozoic Belt Supergroup. These sediments are known to host important SEDEX (e.g., Sullivan) and red-bed copper (e.g., Spar Lake, Rock Creek, Montanore) deposits rich in Ag-Pb- Zn-Cu-Ba. The HHVF erupted through and deposited on the Belt strata during a period of Oligocene extension. Outcrops and drill core samples from Hog Heaven show alteration patterns characteristic of volcanic-hosted, high-sulfidation epithermal deposits. Vuggy quartz transitions laterally into quartz-alunite alteration where large sanidine phenocrysts (up to 4 cm) have been replaced by fine-grained, pink alunite, and/or argillic alteration that is marked by an abundance of white kaolinite-dickite clay. -
Alkali Pyroxenes and Amphiboles: a Window on Rare
Alkali pyroxenes and amphiboles: a window on rare earth elements and other high field strength elements behavior through the magmatic-hydrothermal transition of peralkaline granitic systems Cyrielle Bernard, Guillaume Estrade, Stefano Salvi, Didier Béziat, Martin Smith To cite this version: Cyrielle Bernard, Guillaume Estrade, Stefano Salvi, Didier Béziat, Martin Smith. Alkali pyroxenes and amphiboles: a window on rare earth elements and other high field strength elements behavior through the magmatic-hydrothermal transition of peralkaline granitic systems. Contributions to Mineralogy and Petrology, Springer Verlag, 2020, 10.1007/s00410-020-01723-y. hal-02989854 HAL Id: hal-02989854 https://hal.archives-ouvertes.fr/hal-02989854 Submitted on 5 Nov 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. 1 Alkali pyroxenes and amphiboles: a window on Rare Earth Elements and other High Field Strength 2 Elements behavior through the magmatic-hydrothermal transition of peralkaline granitic systems 3 4 Cyrielle Bernarda, Guillaume Estradea⸸, Stefano Salvia, Didier Béziata , Martin Smithb 5 a GET, CNRS, UPS, Université de Toulouse III, Toulouse, France 6 b School of Environment and Technology, University of Brighton, Brighton, BN2 4GJ, UK 7 8 ⸸ Corresponding author: [email protected] 9 ORCID: 0000-0001-6907-7469 10 11 12 Acknowledgments 13 This work was supported by an INSU/TelluS grant from CNRS (French National Center for Scientific 14 Research). -
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 -
Mapping Phyllosilicates and Aqueous Alteration Products at Tyrrhena Terra, Mars
52nd Lunar and Planetary Science Conference 2021 (LPI Contrib. No. 2548) 1323.pdf MAPPING PHYLLOSILICATES AND AQUEOUS ALTERATION PRODUCTS AT TYRRHENA TERRA, MARS. F. H. Grant1 and J. L. Bishop2, 1University of California, Los Angeles (Los Angeles, CA; [email protected]), 2SETI Institute (Mountain View, CA). Summary: Outcrops of phyllosilicates and small sites of less common aqueous alteration minerals were mapped at Tyrrhena Terra on Mars using CRISM pa- rameters, and CRISM spectral data were collected to more closely analyze the mineralogy in this region. Fe- and Mg-rich smectite and chlorite group phyllosilicates are both detected at Tyrrhena Terra, including sapo- nite, chamosite, and clinochlore. Zeolites and car- bonates are among the rarer alteration minerals also observed at Tyrrhena Terra that further constrain the alteration history in this region. More chlorite than smectite is observed, indicating higher temperature alteration processes occurred at Tyrrhena Terra. Introduction: Tyrrhena Terra is a region in the southern hemisphere of Mars, between the Isidis and Hellas impact basins and south of Libya Montes. The selected study site (Fig. 1) is of particular interest be- cause it has a large concentration of phyllosilicate minerals exposed on the surface, among small outcrops of rarer aqueous alteration minerals [1]. Phyllosilicates are a crucial mineral group to study when striving to understand the aqueous alteration history of a region. Less common aqueous alteration minerals, including zeolite, carbonate, and hydrated sulfates, are also im- portant to further constrain the alteration history of a region [2]. For this research project, we focused pri- marily on identifying the phyllosilicate minerals smec- tite and chlorite. -
NMAM 9000: Asbestos, Chrysotile By
ASBESTOS, CHRYSOTILE by XRD 9000 MW: ~283 CAS: 12001-29-5 RTECS: CI6478500 METHOD: 9000, Issue 3 EVALUATION: FULL Issue 1: 15 May 1989 Issue 3: 20 October 2015 EPA Standard (Bulk): 1% by weight PROPERTIES: Solid, fibrous mineral; conversion to forsterite at 580 °C; attacked by acids; loses water above 300 °C SYNONYMS: Chrysotile SAMPLING MEASUREMENT BULK TECHNIQUE: X-RAY POWDER DIFFRACTION SAMPLE: 1 g to 10 g ANALYTE: Chrysotile SHIPMENT: Seal securely to prevent escape of asbestos PREPARATION: Grind under liquid nitrogen; wet-sieve SAMPLE through 10 µm sieve STABILITY: Indefinitely DEPOSIT: 5 mg dust on 0.45 µm silver membrane BLANKS: None required filter ACCURACY XRD: Copper target X-ray tube; optimize for intensity; 1° slit; integrated intensity with RANGE STUDIED: 1% to 100% in talc [1] background subtraction BIAS: Negligible if standards and samples are CALIBRATION: Suspensions of asbestos in 2-propanol matched in particle size [1] RANGE: 1% to 100% asbestos OVERALL PRECISION ( ): Unknown; depends on matrix and ESTIMATED LOD: 0.2% asbestos in talc and calcite; 0.4% concentration asbestos in heavy X-ray absorbers such as ferric oxide ACCURACY: ±14% to ±25% PRECISION ( ): 0.07 (5% to 100% asbestos); 0.10 (@ 3% asbestos); 0.125 (@ 1% asbestos) APPLICABILITY: Analysis of percent chrysotile asbestos in bulk samples. INTERFERENCES: Antigorite (massive serpentine), chlorite, kaolinite, bementite, and brushite interfere. X-ray fluorescence and absorption is a problem with some elements; fluorescence can be circumvented with a diffracted beam monochromator, and absorption is corrected for in this method. OTHER METHODS: This is NIOSH method P&CAM 309 [2] applied to bulk samples only, since the sensitivity is not adequate for personal air samples. -
Fluid Mixing and the Deep Biosphere of a Fossil Lost City-Type Hydrothermal System at the Iberia Margin
Fluid mixing and the deep biosphere of a fossil Lost City-type hydrothermal system at the Iberia Margin Frieder Kleina,1, Susan E. Humphrisb, Weifu Guob, Florence Schubotzc, Esther M. Schwarzenbachd, and William D. Orsia aDepartment of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, Woods Hole, MA 02543; bDepartment of Geology and Geophysics, Woods Hole Oceanographic Institution, Woods Hole, MA 02543; cDepartment of Geosciences and Center for Marine Environmental Sciences, University of Bremen, 28334 Bremen, Germany; and dDepartment of Geosciences, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061 Edited by David M. Karl, University of Hawaii, Honolulu, HI, and approved August 4, 2015 (received for review March 7, 2015) Subseafloor mixing of reduced hydrothermal fluids with seawater is aging, brucite undersaturated in seawater dissolves and aragonite believed to provide the energy and substrates needed to support recrystallizes to calcite (7). deep chemolithoautotrophic life in the hydrated oceanic mantle (i.e., Actively venting chimneys host a microbial community with a serpentinite). However, geosphere-biosphere interactions in serpen- relatively high proportion of methanogenic archaea (the Lost tinite-hosted subseafloor mixing zones remain poorly constrained. City Methanosarcinales), methanotrophic bacteria, and sulfur- Here we examine fossil microbial communities and fluid mixing oxidizing bacteria, whereas typical sulfate-reducing bacteria are processes in the subseafloor of a Cretaceous Lost City-type hydro- rare (8–10). Geochemical evidence for significant microbial sulfate thermal system at the magma-poor passive Iberia Margin (Ocean reduction in basement lithologies and distinct microbial commu- Drilling Program Leg 149, Hole 897D). Brucite−calcite mineral assem- nities in Lost City vent fluids and chimneys suggest that subsurface blages precipitated from mixed fluids ca. -
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.