Editorial for Special Issue “Mineralogy of Meteorites”
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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. -
U-Pb Age, Re-Os Isotopes, and Hse Geochemistry of Northwest Africa 6704
44th Lunar and Planetary Science Conference (2013) 1841.pdf U-PB AGE, RE-OS ISOTOPES, AND HSE GEOCHEMISTRY OF NORTHWEST AFRICA 6704. T. Iizuka1, Y. Amelin2, I. S. Puchtel3, R. J. Walker3, A. J. Irving4, A. Yamaguchi5, Y. Takagi6, T. Noguchi6 and M. Kimura5. 1Department of Earth and Planetary Science, University of Tokyo, Hongo 7-3-1, Bunkyo, Tokyo 113-0033, Japan ([email protected]), 2Research School of Earth Sciences, Australian National University, Canberra ACT, Australia, 3Department of Geology, University of Maryland, College Park, MD, USA, 4Department of Earth and Space Sciences, University of Washington, Seattle, WA, USA, 5National Institute of Polar Research, Tachikawa, Tokyo 190-8518, Japan, 6College of Science, Ibaraki University, Bunkyo 2-1-1, Mito, Ibaraki 310-8512, Japan. Introduction: Northwest Africa (NWA) 6704 is a of Maryland using standard high temperature acid diges- very unusual ungrouped fresh achondrite. It consists of tion, chemical purification and mass spectrometry tech- abundant coarse-grained (up to 1.5 mm) low-Ca py- niques [3]. The quantities of each of the HSE was at roxene, less abundant olivine, chromite, merrillite and least 1000 times greater than the blanks measured at the interstitial sodic plagioclase. Minor minerals are same time. Thus, blanks had no impact on the measure- awaruite, heazlewoodite, and pentlandite. Raman spec- ments. Accuracy and precision of Ir, Ru, Pt and Pd con- troscopy shows that a majority of the low-Ca pyroxene centrations are estimated to be <2%, of Re <0.4%, and is orthopyroxene. Bulk major element abundances are of Os <0.1%. -
Sulfide/Silicate Melt Partitioning During Enstatite Chondrite Melting
61st Annual Meteoritical Society Meeting 5255.pdf SULFIDE/SILICATE MELT PARTITIONING DURING ENSTATITE CHONDRITE MELTING. C. Floss1, R. A. Fogel2, G. Crozaz1, M. Weisberg2, and M. Prinz2, 1McDonnell Center for the Space Sciences and Department of Earth and Planetary Sciences, Washington University, St. Louis MO 63130, USA ([email protected]), 2American Museum of Natural History, Department of Earth and Planetary Sciences, New York NY 10024, USA. Introduction: Aubrites are igneous rocks thought (present only in CaS-saturated charges) has a flat REE to have formed from an enstatite chondrite-like pattern with abundances of about 0.5 x CI. precursor [1]. Yet their origin remains poorly Discussion: Oldhamite/glass D values are close to understood, at least partly because of confusion over 1 for most REE, consistent with previous results the role played by sulfides, particularly oldhamite. [4,5,6], and significantly lower than those expected CaS in aubrites contains high rare earth element based on REE abundances in aubritic oldhamite. In (REE) abundances and exhibits a variety of patterns contrast, D values for FeS are surprisingly high (from [2] that reflect, to some extent, those seen in about 0.1 to 1), given the low REE abundances of oldhamite from enstatite chondrites [3]. However, natural troilite. FeS/silicate partition coefficients experimental work suggests that CaS/silicate melt reported by [5] are somewhat lower, but exhibit a REE partition coefficients are too low to account for similar pattern. Alkali loss from the charges, the high abundances observed [4,5] and do not explain resulting in Ca-enriched glass, might provide a partial the variable patterns. -
Zinc and Copper Isotopic Fractionation During Planetary Differentiation Heng Chen Washington University in St
Washington University in St. Louis Washington University Open Scholarship Arts & Sciences Electronic Theses and Dissertations Arts & Sciences Winter 12-15-2014 Zinc and Copper Isotopic Fractionation during Planetary Differentiation Heng Chen Washington University in St. Louis Follow this and additional works at: https://openscholarship.wustl.edu/art_sci_etds Part of the Earth Sciences Commons Recommended Citation Chen, Heng, "Zinc and Copper Isotopic Fractionation during Planetary Differentiation" (2014). Arts & Sciences Electronic Theses and Dissertations. 360. https://openscholarship.wustl.edu/art_sci_etds/360 This Dissertation is brought to you for free and open access by the Arts & Sciences at Washington University Open Scholarship. It has been accepted for inclusion in Arts & Sciences Electronic Theses and Dissertations by an authorized administrator of Washington University Open Scholarship. For more information, please contact [email protected]. WASHINGTON UNIVERSITY IN ST. LOUIS Department of Earth and Planetary Sciences Dissertation Examination Committee: Bradley L. Jolliff, Chair Jeffrey G. Catalano Bruce Fegley, Jr. Michael J. Krawczynski Frédéric Moynier Zinc and Copper Isotopic Fractionation during Planetary Differentiation by Heng Chen A dissertation presented to the Graduate School of Arts & Sciences of Washington University in partial fulfillment of the requirements for the degree of Doctor of Philosophy December 2014 St. Louis, Missouri Copyright © 2014, Heng Chen All rights reserved. Table of Contents LIST OF FIGURES -
Warren and Taylor-2014-In Tog-The Moon-'Author's Personal Copy'.Pdf
This article was originally published in Treatise on Geochemistry, Second Edition published by Elsevier, and the attached copy is provided by Elsevier for the author's benefit and for the benefit of the author's institution, for non- commercial research and educational use including without limitation use in instruction at your institution, sending it to specific colleagues who you know, and providing a copy to your institution’s administrator. All other uses, reproduction and distribution, including without limitation commercial reprints, selling or licensing copies or access, or posting on open internet sites, your personal or institution’s website or repository, are prohibited. For exceptions, permission may be sought for such use through Elsevier's permissions site at: http://www.elsevier.com/locate/permissionusematerial Warren P.H., and Taylor G.J. (2014) The Moon. In: Holland H.D. and Turekian K.K. (eds.) Treatise on Geochemistry, Second Edition, vol. 2, pp. 213-250. Oxford: Elsevier. © 2014 Elsevier Ltd. All rights reserved. Author's personal copy 2.9 The Moon PH Warren, University of California, Los Angeles, CA, USA GJ Taylor, University of Hawai‘i, Honolulu, HI, USA ã 2014 Elsevier Ltd. All rights reserved. This article is a revision of the previous edition article by P. H. Warren, volume 1, pp. 559–599, © 2003, Elsevier Ltd. 2.9.1 Introduction: The Lunar Context 213 2.9.2 The Lunar Geochemical Database 214 2.9.2.1 Artificially Acquired Samples 214 2.9.2.2 Lunar Meteorites 214 2.9.2.3 Remote-Sensing Data 215 2.9.3 Mare Volcanism -
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 -
Mineral Processing
Mineral Processing Foundations of theory and practice of minerallurgy 1st English edition JAN DRZYMALA, C. Eng., Ph.D., D.Sc. Member of the Polish Mineral Processing Society Wroclaw University of Technology 2007 Translation: J. Drzymala, A. Swatek Reviewer: A. Luszczkiewicz Published as supplied by the author ©Copyright by Jan Drzymala, Wroclaw 2007 Computer typesetting: Danuta Szyszka Cover design: Danuta Szyszka Cover photo: Sebastian Bożek Oficyna Wydawnicza Politechniki Wrocławskiej Wybrzeze Wyspianskiego 27 50-370 Wroclaw Any part of this publication can be used in any form by any means provided that the usage is acknowledged by the citation: Drzymala, J., Mineral Processing, Foundations of theory and practice of minerallurgy, Oficyna Wydawnicza PWr., 2007, www.ig.pwr.wroc.pl/minproc ISBN 978-83-7493-362-9 Contents Introduction ....................................................................................................................9 Part I Introduction to mineral processing .....................................................................13 1. From the Big Bang to mineral processing................................................................14 1.1. The formation of matter ...................................................................................14 1.2. Elementary particles.........................................................................................16 1.3. Molecules .........................................................................................................18 1.4. Solids................................................................................................................19 -
Chromite Crystal Structure and Chemistry Applied As an Exploration Tool
Western University Scholarship@Western Electronic Thesis and Dissertation Repository February 2015 Chromite Crystal Structure and Chemistry applied as an Exploration Tool Patrick H.M. Shepherd The University of Western Ontario Supervisor Dr. Roberta L. Flemming The University of Western Ontario Graduate Program in Geology A thesis submitted in partial fulfillment of the equirr ements for the degree in Master of Science © Patrick H.M. Shepherd 2015 Follow this and additional works at: https://ir.lib.uwo.ca/etd Part of the Geology Commons Recommended Citation Shepherd, Patrick H.M., "Chromite Crystal Structure and Chemistry applied as an Exploration Tool" (2015). Electronic Thesis and Dissertation Repository. 2685. https://ir.lib.uwo.ca/etd/2685 This Dissertation/Thesis is brought to you for free and open access by Scholarship@Western. It has been accepted for inclusion in Electronic Thesis and Dissertation Repository by an authorized administrator of Scholarship@Western. For more information, please contact [email protected]. Western University Scholarship@Western University of Western Ontario - Electronic Thesis and Dissertation Repository Chromite Crystal Structure and Chemistry Applied as an Exploration Tool Patrick H.M. Shepherd Supervisor Roberta Flemming The University of Western Ontario Follow this and additional works at: http://ir.lib.uwo.ca/etd Part of the Geology Commons This Thesis is brought to you for free and open access by Scholarship@Western. It has been accepted for inclusion in University of Western Ontario - Electronic Thesis and Dissertation Repository by an authorized administrator of Scholarship@Western. For more information, please contact [email protected]. Chromite Crystal Structure and Chemistry Applied as an Exploration Tool (Thesis format: Integrated Article) by Patrick H.M. -
List of New Mineral Names: with an Index of Authors
415 A (fifth) list of new mineral names: with an index of authors. 1 By L. J. S~v.scs~, M.A., F.G.S. Assistant in the ~Iineral Department of the,Brltish Museum. [Communicated June 7, 1910.] Aglaurito. R. Handmann, 1907. Zeita. Min. Geol. Stuttgart, col. i, p. 78. Orthoc]ase-felspar with a fine blue reflection forming a constituent of quartz-porphyry (Aglauritporphyr) from Teplitz, Bohemia. Named from ~,Xavpo~ ---- ~Xa&, bright. Alaito. K. A. ~Yenadkevi~, 1909. BuU. Acad. Sci. Saint-P6tersbourg, ser. 6, col. iii, p. 185 (A~am~s). Hydrate~l vanadic oxide, V205. H~O, forming blood=red, mossy growths with silky lustre. Founi] with turanite (q. v.) in thct neighbourhood of the Alai Mountains, Russian Central Asia. Alamosite. C. Palaehe and H. E. Merwin, 1909. Amer. Journ. Sci., ser. 4, col. xxvii, p. 899; Zeits. Kryst. Min., col. xlvi, p. 518. Lead recta-silicate, PbSiOs, occurring as snow-white, radially fibrous masses. Crystals are monoclinic, though apparently not isom0rphous with wol]astonite. From Alamos, Sonora, Mexico. Prepared artificially by S. Hilpert and P. Weiller, Ber. Deutsch. Chem. Ges., 1909, col. xlii, p. 2969. Aloisiite. L. Colomba, 1908. Rend. B. Accad. Lincei, Roma, set. 5, col. xvii, sere. 2, p. 233. A hydrated sub-silicate of calcium, ferrous iron, magnesium, sodium, and hydrogen, (R pp, R',), SiO,, occurring in an amorphous condition, intimately mixed with oalcinm carbonate, in a palagonite-tuff at Fort Portal, Uganda. Named in honour of H.R.H. Prince Luigi Amedeo of Savoy, Duke of Abruzzi. Aloisius or Aloysius is a Latin form of Luigi or I~ewis. -
NEW MINERAL NAMES Mrcnnnr Fr-Brscnpn
THE AMERICAN MINERAI,OGIST, VOL. 55, JANUARY-FEBRUARY, 1970 NEW MINERAL NAMES Mrcnnnr Fr-Brscnpn Barringerite P. R. Busrcr (1969) Phosphide from meteorites.' Barringerite, a new iron-nickel mineral. Sci,ence165, 169-17 1,. The average of microprobe analyses was Fe 44.3*0.9, Ni 33.9+0.7, Co 0.25+0.03, P 21.8+0.4, stm 10O.25/6,corresponding to (Irer.roNio.srCoo.n)P,or (Fe, Ni)rP. X-ray study shows it to be hexagonal,space group P62 m, a 5.87 -t0.07, c 3.M+0.04 ft. The strongest X-ray lines (including many overlapping troilite or schreibersite; those starred do not overlap) are 2.98 (110),2.85* (101),2.53(200),2.23(lll),2.03*(201), 1.88* (r20), r.72(t00), 1.68(300, t2r), L.48(220), t.4t(3t0, 22r), r.29*(31r), 1.28(122), t.27 (400), 1.205(302),1.197(4oD.The structure is similar to those of synthetic FerP and NirP. p (calc) 6.92. Color white, very similar to that of kamacite, bluish compared to schreibersite. Harder than either kamacite or schreibersite. Reflectivity in air and oil slightly higher than that of schreibersite, lower than that of kamacite. Noticeably anisotropic (white to blue). Bireflectance not observed. The mineral occurs as bands 10-15 pm wide and several hundred microns long; they consist of individual grains less than 1 pm in diameter. They occur in the Ollague pallasite along the contacts between schreibersite and troilite. The name is for D. -
Iron Meteorites
Meteoritics & Planetary Science 42, Nr 7/8, 1441–1463 (2007) Abstract available online at http://meteoritics.org Trace element studies of silicate-rich inclusions in the Guin (UNGR) and Kodaikanal (IIE) iron meteorites Gero KURAT1*, Ernst ZINNER2, and Maria Eugenia VARELA3 1Department of Lithospheric Sciences, University of Vienna, Althanstrasse 14, A-1090 Vienna, Austria 2Laboratory for Space Sciences and Physics Department, Washington University, Saint Louis, Missouri 63130, USA 3Complejo Astronómico El Leoncito (CASLEO), Av. España 1512 sur, J5402DSP, San Juan, Argentina *Corresponding author. E-mail: [email protected] (Received 30 October 2006; revision accepted 20 June 2007) Abstract–A devitrified glass inclusion from the Guin (UNGR) iron consists of cryptocrystalline feldspars, pyroxenes, and silica and is rich in SiO2, Al2O3, and Na2O. It contains a rutile grain and is in contact with a large Cl apatite. The latter is very rich in rare earth elements (REEs) (~80 × CI), which display a flat abundance pattern, except for Eu and Yb, which are underabundant. The devitrified glass is very poor in REEs (<0.1 × CI), except for Eu and Yb, which have positive abundance anomalies. Devitrified glass and Cl apatite are out of chemical equilibrium and their complementary REE patterns indicate a genesis via condensation under reducing conditions. Inclusion 1 in the Kodaikanal (IIE) iron consists of glass only, whereas inclusion 2 consists of clinopyroxene, which is partly overgrown by low-Ca pyroxene, and apatite embedded in devitrified glass. All minerals are euhedral or have skeletal habits indicating crystallization from the liquid precursor of the glass. Pyroxenes and the apatite are rich in trace elements, indicating crystallization from a liquid that had 10–50 × CI abundances of REEs and refractory lithophile elements (RLEs). -
Physical Properties of Martian Meteorites: Porosity and Density Measurements
Meteoritics & Planetary Science 42, Nr 12, 2043–2054 (2007) Abstract available online at http://meteoritics.org Physical properties of Martian meteorites: Porosity and density measurements Ian M. COULSON1, 2*, Martin BEECH3, and Wenshuang NIE3 1Solid Earth Studies Laboratory (SESL), Department of Geology, University of Regina, Regina, Saskatchewan S4S 0A2, Canada 2Institut für Geowissenschaften, Universität Tübingen, 72074 Tübingen, Germany 3Campion College, University of Regina, Regina, Saskatchewan S4S 0A2, Canada *Corresponding author. E-mail: [email protected] (Received 11 September 2006; revision accepted 06 June 2007) Abstract–Martian meteorites are fragments of the Martian crust. These samples represent igneous rocks, much like basalt. As such, many laboratory techniques designed for the study of Earth materials have been applied to these meteorites. Despite numerous studies of Martian meteorites, little data exists on their basic structural characteristics, such as porosity or density, information that is important in interpreting their origin, shock modification, and cosmic ray exposure history. Analysis of these meteorites provides both insight into the various lithologies present as well as the impact history of the planet’s surface. We present new data relating to the physical characteristics of twelve Martian meteorites. Porosity was determined via a combination of scanning electron microscope (SEM) imagery/image analysis and helium pycnometry, coupled with a modified Archimedean method for bulk density measurements. Our results show a range in porosity and density values and that porosity tends to increase toward the edge of the sample. Preliminary interpretation of the data demonstrates good agreement between porosity measured at 100× and 300× magnification for the shergottite group, while others exhibit more variability.