An Evolutionary System of Mineralogy, Part V: Aqueous and Thermal Alteration of Planetesimals (~4565 to 4550
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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%. -
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. -
Iron.Rich Amesite from the Lake Asbestos Mine. Black
Canodian Mineralogist Yol.22, pp. 43742 (1984) IRON.RICHAMESITE FROM THE LAKE ASBESTOS MINE. BLACKLAKE. OUEBEC MEHMET YEYZT TANER,* AND ROGER LAURENT DAporternentde Gdologie,Universitd Loval, Qudbec,Qudbec GIK 7P4 ABSTRACT o 90.02(1l)', P W.42(12)',1 89.96(8)'.A notreconnais- sance,c'est la premibrefois qu'on ddcritune am6site riche Iron-rich amesite is found in a metasomatically altered enfer. Elles'ct form€ependant l'altdration hydrothermale granite sheet20 to 40 cm thick emplacedin serpentinite of du granitedans la serpentinite,dans les m€mes conditions the Thetford Mi[es ophiolite complex at the Lake Asbestos debasses pression et temperaturequi ont prdsid6d la for- mine (z16o01'N,11"22' W) ntheQuebec Appalachians.The mation de la rodingite dansle granite et de I'amiante- amesiteis associatedsdth 4lodingife 6semblage(grossu- chrysotiledans la serpentinite. lar + calcite t diopside t clinozoisite) that has replaced the primary minerals of the granite. The Quebec amesite Mots-clds:am6site, rodingite, granite, complexeophio- occurs as subhedral grains 2@ to 6@ pm.in diameter that litique, Thetford Mines, Qu6bec. have a tabular habit. It is optically positive with a small 2V, a 1.612,1 1.630,(t -'o = 0.018).Its structuralfor- INTRoDUc"iloN mula, calculated from electron-microprobe data, is: (Mg1.1Fe6.eA1s.e)(Alo.esil.df Os(OH)r.2. X-ray powder- Amesite is a raxehydrated aluminosilicate of mag- diffraction yield data dvalues that are systematicallygreater nesium in which some ferrous iron usually is found than those of amesitefrom Chester, Massachusetts,prob- replacingmapesium. The extent of this replacement ably becauseof the partial replacement of Mg by Fe. -
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. -
74275 Oriented Ilmenite Basalt 1493 Grams
74275 Oriented Ilmenite Basalt 1493 grams 74275 Figure 1: Location of basalt sample 74275 at Shorty Crater - also see 74220. (falce color) AS17-137-20990 Introduction 1981). This sample has proven useful to studies that 74275 is a fine-grained, high-Ti mare basalt with require known lunar orientation with extended significant armalcolite content (Hodges and Kushiro exposure history to the extra-lunar environment 1974; Neal and Taylor 1993). It contains vesicles, vugs (micrometeorites, cosmic rays, solar irradiation). The and unusual olivine megacrysts (Fo82) (Meyer and sample is relatively flat 17 by 12 cm and 4 cm thick. Wilshire 1974). The top (T1) surface is somewhat rounded and has many micrometeorite pits (figure 4), while the bottom 74275 was collected from the rim of Shorty Crater (B1) surface is flat and angular and without any (figure 1) and was photographed both on the lunar evidence of exposure to the micrometeorites (figure surface and in the laboratory (with similar lighting) to 5). Fink et al. (1998) have carefully considered the document the exact lunar orientation. (Wolfe et al. exact orientation (30 deg tilt), shielding (nearby Lunar Sample Compendium C Meyer 2011 boulder) and detailed exposure history (complex) of 74275 74275. Di Hd This basalt has been determined to be very old (> 3.8 b.y.). Based on trace element analysis it is a type C Apollo 17 basalt. Petrography Perhaps the best petrographic description of 74275 is En Fs given by Hodges and Kushiro (1974): “Rock 74275 is a fine-grained ilmenite basalt with microphenocrysts Fo Fa of olivine (Fo80-71), titanaugite (up to 6.8 wt. -
POSTER SESSION 5:30 P.M
Monday, July 27, 1998 POSTER SESSION 5:30 p.m. Edmund Burke Theatre Concourse MARTIAN AND SNC METEORITES Head J. W. III Smith D. Zuber M. MOLA Science Team Mars: Assessing Evidence for an Ancient Northern Ocean with MOLA Data Varela M. E. Clocchiatti R. Kurat G. Massare D. Glass-bearing Inclusions in Chassigny Olivine: Heating Experiments Suggest Nonigneous Origin Boctor N. Z. Fei Y. Bertka C. M. Alexander C. M. O’D. Hauri E. Shock Metamorphic Features in Lithologies A, B, and C of Martian Meteorite Elephant Moraine 79001 Flynn G. J. Keller L. P. Jacobsen C. Wirick S. Carbon in Allan Hills 84001 Carbonate and Rims Terho M. Magnetic Properties and Paleointensity Studies of Two SNC Meteorites Britt D. T. Geological Results of the Mars Pathfinder Mission Wright I. P. Grady M. M. Pillinger C. T. Further Carbon-Isotopic Measurements of Carbonates in Allan Hills 84001 Burckle L. H. Delaney J. S. Microfossils in Chondritic Meteorites from Antarctica? Stay Tuned CHONDRULES Srinivasan G. Bischoff A. Magnesium-Aluminum Study of Hibonites Within a Chondrulelike Object from Sharps (H3) Mikouchi T. Fujita K. Miyamoto M. Preferred-oriented Olivines in a Porphyritic Olivine Chondrule from the Semarkona (LL3.0) Chondrite Tachibana S. Tsuchiyama A. Measurements of Evaporation Rates of Sulfur from Iron-Iron Sulfide Melt Maruyama S. Yurimoto H. Sueno S. Spinel-bearing Chondrules in the Allende Meteorite Semenenko V. P. Perron C. Girich A. L. Carbon-rich Fine-grained Clasts in the Krymka (LL3) Chondrite Bukovanská M. Nemec I. Šolc M. Study of Some Achondrites and Chondrites by Fourier Transform Infrared Microspectroscopy and Diffuse Reflectance Spectroscopy Semenenko V. -
Occurrence, Alteration Patterns and Compositional Variation of Perovskite in Kimberlites
975 The Canadian Mineralogist Vol. 38, pp. 975-994 (2000) OCCURRENCE, ALTERATION PATTERNS AND COMPOSITIONAL VARIATION OF PEROVSKITE IN KIMBERLITES ANTON R. CHAKHMOURADIAN§ AND ROGER H. MITCHELL Department of Geology, Lakehead University, 955 Oliver Road, Thunder Bay, Ontario P7B 5E1, Canada ABSTRACT The present work summarizes a detailed investigation of perovskite from a representative collection of kimberlites, including samples from over forty localities worldwide. The most common modes of occurrence of perovskite in archetypal kimberlites are discrete crystals set in a serpentine–calcite mesostasis, and reaction-induced rims on earlier-crystallized oxide minerals (typically ferroan geikielite or magnesian ilmenite). Perovskite precipitates later than macrocrystal spinel (aluminous magnesian chromite), and nearly simultaneously with “reaction” Fe-rich spinel (sensu stricto), and groundmass spinels belonging to the magnesian ulvöspinel – magnetite series. In most cases, perovskite crystallization ceases prior to the resorption of groundmass spinels and formation of the atoll rim. During the final evolutionary stages, perovskite commonly becomes unstable and reacts with a CO2- rich fluid. Alteration of perovskite in kimberlites involves resorption, cation leaching and replacement by late-stage minerals, typically TiO2, ilmenite, titanite and calcite. Replacement reactions are believed to take place at temperatures below 350°C, 2+ P < 2 kbar, and over a wide range of a(Mg ) values. Perovskite from kimberlites approaches the ideal formula CaTiO3, and normally contains less than 7 mol.% of other end-members, primarily lueshite (NaNbO3), loparite (Na0.5Ce0.5TiO3), and CeFeO3. Evolutionary trends exhibited by perovskite from most localities are relatively insignificant and typically involve a decrease in REE and Th contents toward the rim (normal pattern of zonation). -
Petrology of Nepheline Syenite Pegmatites in the Oslo Rift, Norway: Zr and Ti Mineral Assemblages in Miaskitic and Agpaitic Pegmatites in the Larvik Plutonic Complex
MINERALOGIA, 44, No 3-4: 61-98, (2013) DOI: 10.2478/mipo-2013-0007 www.Mineralogia.pl MINERALOGICAL SOCIETY OF POLAND POLSKIE TOWARZYSTWO MINERALOGICZNE __________________________________________________________________________________________________________________________ Original paper Petrology of nepheline syenite pegmatites in the Oslo Rift, Norway: Zr and Ti mineral assemblages in miaskitic and agpaitic pegmatites in the Larvik Plutonic Complex Tom ANDERSEN1*, Muriel ERAMBERT1, Alf Olav LARSEN2, Rune S. SELBEKK3 1 Department of Geosciences, University of Oslo, PO Box 1047 Blindern, N-0316 Oslo Norway; e-mail: [email protected] 2 Statoil ASA, Hydroveien 67, N-3908 Porsgrunn, Norway 3 Natural History Museum, University of Oslo, Sars gate 1, N-0562 Oslo, Norway * Corresponding author Received: December, 2010 Received in revised form: May 15, 2012 Accepted: June 1, 2012 Available online: November 5, 2012 Abstract. Agpaitic nepheline syenites have complex, Na-Ca-Zr-Ti minerals as the main hosts for zirconium and titanium, rather than zircon and titanite, which are characteristic for miaskitic rocks. The transition from a miaskitic to an agpaitic crystallization regime in silica-undersaturated magma has traditionally been related to increasing peralkalinity of the magma, but halogen and water contents are also important parameters. The Larvik Plutonic Complex (LPC) in the Permian Oslo Rift, Norway consists of intrusions of hypersolvus monzonite (larvikite), nepheline monzonite (lardalite) and nepheline syenite. Pegmatites ranging in composition from miaskitic syenite with or without nepheline to mildly agpaitic nepheline syenite are the latest products of magmatic differentiation in the complex. The pegmatites can be grouped in (at least) four distinct suites from their magmatic Ti and Zr silicate mineral assemblages. -
A Review of the Structural Architecture of Tellurium Oxycompounds
Mineralogical Magazine, May 2016, Vol. 80(3), pp. 415–545 REVIEW OPEN ACCESS A review of the structural architecture of tellurium oxycompounds 1 2,* 3 A. G. CHRISTY ,S.J.MILLS AND A. R. KAMPF 1 Research School of Earth Sciences and Department of Applied Mathematics, Research School of Physics and Engineering, Australian National University, Canberra, ACT 2601, Australia 2 Geosciences, Museum Victoria, GPO Box 666, Melbourne, Victoria 3001, Australia 3 Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, CA 90007, USA [Received 24 November 2015; Accepted 23 February 2016; Associate Editor: Mark Welch] ABSTRACT Relative to its extremely low abundance in the Earth’s crust, tellurium is the most mineralogically diverse chemical element, with over 160 mineral species known that contain essential Te, many of them with unique crystal structures. We review the crystal structures of 703 tellurium oxysalts for which good refinements exist, including 55 that are known to occur as minerals. The dataset is restricted to compounds where oxygen is the only ligand that is strongly bound to Te, but most of the Periodic Table is represented in the compounds that are reviewed. The dataset contains 375 structures that contain only Te4+ cations and 302 with only Te6+, with 26 of the compounds containing Te in both valence states. Te6+ was almost exclusively in rather regular octahedral coordination by oxygen ligands, with only two instances each of 4- and 5-coordination. Conversely, the lone-pair cation Te4+ displayed irregular coordination, with a broad range of coordination numbers and bond distances. -
Invited Review
INVITED REVIEW Presolar grains from meteorites: Remnants from the early times of the solar system Katharina Lodders a,* and Sachiko Amari b a Planetary Chemistry Laboratory, Department of Earth and Planetary Sciences and McDonnell Center for the Space Sciences, Washington University, Campus Box 1169, One Brookings Drive, St. Louis, MO 63130, USA b Department of Physics and McDonnell Center for the Space Sciences, Washington University, Campus Box 1105, One Brookings Drive, St. Louis, MO 63130, USA Received 5 October 2004; accepted 4 January 2005 Abstract This review provides an introduction to presolar grains – preserved stardust from the interstellar molecular cloud from which our solar system formed – found in primitive meteorites. We describe the search for the presolar components, the currently known presolar mineral populations, and the chemical and isotopic characteristics of the grains and dust-forming stars to identify the grains’ most probable stellar sources. Keywords: Presolar grains; Interstellar dust; Asymptotic giant branch (AGB) stars; Novae; Supernovae; Nucleosynthesis; Isotopic ratios; Meteorites 1. Introduction The history of our solar system started with the gravitational collapse of an interstellar molecular cloud laden with gas and dust supplied from dying stars. The dust from this cloud is the topic of this review. A small fraction of this dust escaped destruction during the many processes that occurred after molecular cloud collapse about 4.55 Ga ago. We define presolar grains as stardust that formed in stellar outflows or ejecta and remained intact throughout its journey into the solar system where it was preserved in meteorites. The survival and presence of genuine stardust in meteorites was not expected in the early years of meteorite studies.