Asteroid 2008 TC3—Almahata Sitta: a Spectacular Breccia Containing Many Different Ureilitic and Chondritic Lithologies
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A New Sulfide Mineral (Mncr2s4) from the Social Circle IVA Iron Meteorite
American Mineralogist, Volume 101, pages 1217–1221, 2016 Joegoldsteinite: A new sulfide mineral (MnCr2S4) from the Social Circle IVA iron meteorite Junko Isa1,*, Chi Ma2,*, and Alan E. Rubin1,3 1Department of Earth, Planetary, and Space Sciences, University of California, Los Angeles, California 90095, U.S.A. 2Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California 91125, U.S.A. 3Institute of Geophysics and Planetary Physics, University of California, Los Angeles, California 90095, U.S.A. Abstract Joegoldsteinite, a new sulfide mineral of end-member formula MnCr2S4, was discovered in the 2+ Social Circle IVA iron meteorite. It is a thiospinel, the Mn analog of daubréelite (Fe Cr2S4), and a new member of the linnaeite group. Tiny grains of joegoldsteinite were also identified in the Indarch EH4 enstatite chondrite. The chemical composition of the Social Circle sample determined by electron microprobe is (wt%) S 44.3, Cr 36.2, Mn 15.8, Fe 4.5, Ni 0.09, Cu 0.08, total 101.0, giving rise to an empirical formula of (Mn0.82Fe0.23)Cr1.99S3.95. The crystal structure, determined by electron backscattered diffraction, is aFd 3m spinel-type structure with a = 10.11 Å, V = 1033.4 Å3, and Z = 8. Keywords: Joegoldsteinite, MnCr2S4, new sulfide mineral, thiospinel, Social Circle IVA iron meteorite, Indarch EH4 enstatite chondrite Introduction new mineral by the International Mineralogical Association (IMA 2015-049) in August 2015. It was named in honor of Thiospinels have a general formula of AB2X4 where A is a divalent metal, B is a trivalent metal, and X is a –2 anion, Joseph (Joe) I. -
Petrography and Mineral Chemistry of Escalón Meteorite, an H4 Chondrite, México
148 Reyes-SalasRevista Mexicana et al. de Ciencias Geológicas, v. 27, núm. 1, 2010, p. 148-161 Petrography and mineral chemistry of Escalón meteorite, an H4 chondrite, México Adela M. Reyes-Salas1,*, Gerardo Sánchez-Rubio1, Patricia Altuzar-Coello2, Fernando Ortega-Gutiérrez1, Daniel Flores-Gutiérrez3, Karina Cervantes-de la Cruz1, Eugenio Reyes4, and Carlos Linares5 1 Universidad Nacional Autónoma de México, Instituto de Geología, Del. Coyoacán, 04510 México D.F., Mexico. 2 Universidad Nacional Autónoma de México, Centro de Investigación en Energía, Campus Temixco, Priv. Xochicalco s/n, 62580 Temixco Morelos, Mexico. 3 Universidad Nacional Autónoma de México, Instituto de Astronomía, Del. Coyoacán, 04510 México D.F., Mexico. 4 Universidad Nacional Autónoma de México, Facultad de Química, Del. Coyoacán, 04510 México D.F., Mexico. 5 Universidad Nacional Autónoma de México, Instituto de Geofísica, Del. Coyoacán, 04510 México D.F., Mexico. * [email protected] ABSTRACT The Escalón meteorite, a crusted mass weighing 54.3 g, was recovered near Zona del Silencio in Escalón, state of Chihuahua, México. The stone is an ordinary chondrite belonging to the high iron group H, type 4. Electron microprobe analyses of olivine (Fa18.1) and pyroxene (Fs16.5), phosphate, plagioclase, opaque phases, matrix and chondrule glasses are presented. The metal phases present are kamacite (6.08 % Ni), taenite (31.66 % Ni), high nickel taenite (50.01 % Ni) and traces of native Cu. The chondrules average apparent diameter measures 0.62 mm. X-ray diffraction pattern shows olivine, pyroxene and kamacite. Alkaline-type glass is found mainly in chondrules. This meteorite is a stage S3, shock-blackened chondrite with weathering grade W0. -
Fe,Mg)S, the IRON-DOMINANT ANALOGUE of NININGERITE
1687 The Canadian Mineralogist Vol. 40, pp. 1687-1692 (2002) THE NEW MINERAL SPECIES KEILITE, (Fe,Mg)S, THE IRON-DOMINANT ANALOGUE OF NININGERITE MASAAKI SHIMIZU§ Department of Earth Sciences, Faculty of Science, Toyama University, 3190 Gofuku, Toyama 930-8555, Japan § HIDETO YOSHIDA Department of Earth and Planetary Science, Graduate School of Science, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan § JOSEPH A. MANDARINO 94 Moore Avenue, Toronto, Ontario M4T 1V3, and Earth Sciences Division, Royal Ontario Museum, 100 Queens’s Park, Toronto, Ontario M5S 2C6, Canada ABSTRACT Keilite, (Fe,Mg)S, is a new mineral species that occurs in several meteorites. The original description of niningerite by Keil & Snetsinger (1967) gave chemical analytical data for “niningerite” in six enstatite chondrites. In three of those six meteorites, namely Abee and Adhi-Kot type EH4 and Saint-Sauveur type EH5, the atomic ratio Fe:Mg has Fe > Mg. Thus this mineral actually represents the iron-dominant analogue of niningerite. By analogy with synthetic MgS and niningerite, keilite is cubic, with space group Fm3m, a 5.20 Å, V 140.6 Å3, Z = 4. Keilite and niningerite occur as grains up to several hundred m across. Because of the small grain-size, most of the usual physical properties could not be determined. Keilite is metallic and opaque; in reflected light, it is isotropic and gray. Point-count analyses of samples of the three meteorites by Keil (1968) gave the following amounts of keilite (in vol.%): Abee 11.2, Adhi-Kot 0.95 and Saint-Sauveur 3.4. -
Silicate-Sio Reaction in a Protoplanetary Disk Recorded by Oxygen Isotopes in Chondrules
Silicate-SiO reaction in a protoplanetary disk recorded by oxygen isotopes in chondrules Ryoji Tanaka1* & Eizo Nakamura1 1The Pheasant Memorial Laboratory for Geochemistry and Cosmochemistry, Institute for Planetary Materials, Okayama University, Misasa, Tottori, 682-0193, Japan *Corresponding author: [email protected] The formation of planetesimals and planetary embryos during the earliest stages of the solar protoplanetary disk largely determined the composition and structure of the terrestrial planets. Within a few million years (Myr) after the birth of the solar system, chondrule formation and accretion of the parent bodies of differentiated achondrites and the terrestrial planets took place in the inner protoplanetary disk1,2. Here we show that, for chondrules in unequilibrated enstatite chondrites, high-precision Δ17O values (deviation of δ17O value from a terrestrial silicate fractionation line) vary significantly (ranging from -0.49 to +0.84‰) and fall on an array with a steep slope of 1.27 on a three oxygen isotope plot. This array can be explained by reaction between an olivine-rich chondrule melt and a SiO-rich gas derived from vaporized dust and nebular gas. Our study suggests that the majority of the building blocks of planetary embryos formed by successive silicate-gas interaction processes: silicate-H2O followed by silicate-SiO interactions under more oxidized and reduced conditions, respectively, within a few Myr after the formation of the solar system. Major precursor components of enstatite chondrites (EC), differentiated planetesimals, Mars, and the Earth are thought to have been formed at similar heliocentric distances3,4. The unequilibrated EC preserve records of nebular conditions in each component (chondrules, Ca- Al-rich inclusions [CAIs], Fe-Ni-metal, and matrix), each of which has not been heavily overprinted by post-accretionary thermal processes. -
Curt Teich Postcard Archives Towns and Cities
Curt Teich Postcard Archives Towns and Cities Alaska Aialik Bay Alaska Highway Alcan Highway Anchorage Arctic Auk Lake Cape Prince of Wales Castle Rock Chilkoot Pass Columbia Glacier Cook Inlet Copper River Cordova Curry Dawson Denali Denali National Park Eagle Fairbanks Five Finger Rapids Gastineau Channel Glacier Bay Glenn Highway Haines Harding Gateway Homer Hoonah Hurricane Gulch Inland Passage Inside Passage Isabel Pass Juneau Katmai National Monument Kenai Kenai Lake Kenai Peninsula Kenai River Kechikan Ketchikan Creek Kodiak Kodiak Island Kotzebue Lake Atlin Lake Bennett Latouche Lynn Canal Matanuska Valley McKinley Park Mendenhall Glacier Miles Canyon Montgomery Mount Blackburn Mount Dewey Mount McKinley Mount McKinley Park Mount O’Neal Mount Sanford Muir Glacier Nome North Slope Noyes Island Nushagak Opelika Palmer Petersburg Pribilof Island Resurrection Bay Richardson Highway Rocy Point St. Michael Sawtooth Mountain Sentinal Island Seward Sitka Sitka National Park Skagway Southeastern Alaska Stikine Rier Sulzer Summit Swift Current Taku Glacier Taku Inlet Taku Lodge Tanana Tanana River Tok Tunnel Mountain Valdez White Pass Whitehorse Wrangell Wrangell Narrow Yukon Yukon River General Views—no specific location Alabama Albany Albertville Alexander City Andalusia Anniston Ashford Athens Attalla Auburn Batesville Bessemer Birmingham Blue Lake Blue Springs Boaz Bobler’s Creek Boyles Brewton Bridgeport Camden Camp Hill Camp Rucker Carbon Hill Castleberry Centerville Centre Chapman Chattahoochee Valley Cheaha State Park Choctaw County -
Calcium Isotopes in Natural and Experimental Carbonated Silicate Melts
Western University Scholarship@Western Electronic Thesis and Dissertation Repository 2-27-2018 2:30 PM Calcium Isotopes in Natural and Experimental Carbonated Silicate Melts Matthew Maloney The University of Western Ontario Supervisor Bouvier, Audrey The University of Western Ontario Co-Supervisor Withers, Tony 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 © Matthew Maloney 2018 Follow this and additional works at: https://ir.lib.uwo.ca/etd Part of the Geochemistry Commons Recommended Citation Maloney, Matthew, "Calcium Isotopes in Natural and Experimental Carbonated Silicate Melts" (2018). Electronic Thesis and Dissertation Repository. 5256. https://ir.lib.uwo.ca/etd/5256 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]. Abstract The calcium stable isotopic compositions of mantle-sourced rocks and minerals were investigated to better understand the carbon cycle in the Earth’s mantle. Bulk carbonatites and kimberlites were analyzed to identify a geochemical signature of carbonatite magmatism, while inter-mineral fractionation was measured in co-existing Ca-bearing carbonate and silicate minerals. Bulk samples show a range of composition deviating from the bulk silicate Earth δ44/40Ca composition indicating signatures of magmatic processes or marine carbonate addition 44/40 to source materials. Δ Cacarbonate-silicate values range from -0.55‰ to +1.82‰ and positively correlate with Ca/Mg ratios in pyroxenes. -
Geological Survey Canada
70-66 GEOLOGICAL PAPER 70-66 ., SURVEY OF CANADA DEPARTMENT OF ENERGY, MINES AND RESOURCES REVISED CATALOGUE OF THE NATIONAL METEORITE COLLECTION OF CANADA LISTING ACQUISITIONS TO AUGUST 31, 1970 J. A. V. Douglas 1971 Price, 75 cents GEOLOGICAL SURVEY OF CANADA CANADA PAPER 70-66 REVISED CATALOGUE OF THE NATIONAL METEORITE COLLECTION OF CANADA LISTING ACQUISITIONS TO AUGUST 31, 1970 J. A. V. Douglas DEPARTMENT OF ENERGY, MINES AND RESOURCES @)Crown Copyrights reserved Available by mail from Information Canada, Ottawa from the Geological Survey of Canada 601 Booth St., Ottawa and Information Canada bookshops in HALIFAX - 1735 Barrington Street MONTREAL - 1182 St. Catherine Street West OTTAWA - 171 Slater Street TORONTO - 221 Yonge Street WINNIPEG - 499 Portage Avenue VANCOUVER - 657 Granville Street or through your bookseller Price: 75 cents Catalogue No. M44-70-66 Price subject to change without notice Information Canada Ottawa 1971 ABSTRACT A catalogue of the National Meteorite Collection of Canada, published in 1963 listed 242 different meteorite specimens. Since then specimens from 50 a dditional meteorites have been added to the collection and several more specimens have been added to the tektite collection. This report describes all specimens in the collection. REVISED CATALOGUE OF THE NATIONAL METEORITE COLLECTION OF CANADA LISTING ACQUISITIONS TO AUGUST 31, 1970 INTRODUCTION At the beginning of the nineteenth century meteorites were recog nized as unique objects worth preserving in collections. Increasingly they have become such valuable objects for investigation in many fields of scienti fic research that a strong international interest in their conservation and pre servation has developed (c. f. -
Noble Gas Study of the Saratov L4 Chondrite
Meteoritics & Planetary Science 45, Nr 3, 361–372 (2010) doi: 10.1111/j.1945-5100.2010.01026.x Noble gas study of the Saratov L4 chondrite Jun-ichi MATSUDA1*, Hidetomo TSUKAMOTO1, Chie MIYAKAWA1, and Sachiko AMARI2 1Department of Earth and Space Science, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043, Japan 2Laboratory for Space Sciences and the Physics Department, Washington University, St. Louis, Missouri 63130, USA *Corresponding author. E-mail: [email protected] (Received 10 September 2008; revision accepted 28 December 2009) Abstract–We have determined the elemental abundances and the isotopic compositions of noble gases in a bulk sample and an HF ⁄ HCl residue of the Saratov (L4) chondrite using stepwise heating. The Ar, Kr, and Xe concentrations in the HF ⁄ HCl residue are two orders of magnitude higher than those in the bulk sample, while He and Ne concentrations from both are comparable. The residue contains only a portion of the trapped heavy noble gases in Saratov; 40 ± 9% for 36Ar, 58 ± 12% for 84Kr, and 48 ± 10% for 132Xe, respectively. The heavy noble gas elemental pattern in the dissolved fraction is similar to that in the residue but has high release temperatures. Xenon isotopic ratios of the HF ⁄ HCl residue indicate that there is no Xe-HL in Saratov, but Ne isotopic ratios in the HF ⁄ HCl residue lie on a straight line connecting the cosmogenic component and a composition between Ne-Q and Ne-HL. This implies that the Ne isotopic composition of Q has been changed by incorporating Ne-HL (Huss et al. -
Asteroid Regolith Weathering: a Large-Scale Observational Investigation
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Doctoral Dissertations Graduate School 5-2019 Asteroid Regolith Weathering: A Large-Scale Observational Investigation Eric Michael MacLennan University of Tennessee, [email protected] Follow this and additional works at: https://trace.tennessee.edu/utk_graddiss Recommended Citation MacLennan, Eric Michael, "Asteroid Regolith Weathering: A Large-Scale Observational Investigation. " PhD diss., University of Tennessee, 2019. https://trace.tennessee.edu/utk_graddiss/5467 This Dissertation is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a dissertation written by Eric Michael MacLennan entitled "Asteroid Regolith Weathering: A Large-Scale Observational Investigation." I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Doctor of Philosophy, with a major in Geology. Joshua P. Emery, Major Professor We have read this dissertation and recommend its acceptance: Jeffrey E. Moersch, Harry Y. McSween Jr., Liem T. Tran Accepted for the Council: Dixie L. Thompson Vice Provost and Dean of the Graduate School (Original signatures are on file with official studentecor r ds.) Asteroid Regolith Weathering: A Large-Scale Observational Investigation A Dissertation Presented for the Doctor of Philosophy Degree The University of Tennessee, Knoxville Eric Michael MacLennan May 2019 © by Eric Michael MacLennan, 2019 All Rights Reserved. -
Sulfides in Enstate Chondrites
Sulfides in Enstatite Chondrites: Indicators of Impact History Kristyn Hill1,2, Emma Bullock2, Cari Corrigan2, and Timothy McCoy2 1Lock Haven University of Pennsylvania, Lock Haven, PA 17745, USA 2National Museum of Natural History, Department of Mineral Sciences, Washington D.C. 20013, USA Introductton Results Discussion Enstatite chondrites are a class of meteorites. They are Determining the history of the parent body of a referred to as chondrites because of the spherical Impact Melt, Slowly Cooled chondritic meteorite often includes distinguishing whether chondrules found in the matrix of the meteorites. Enstatite aa bb cc d d or not the meteorite was impact melted, and the cooling chondrites are the most highly reduced meteorites and rate. contain iron-nickel metal and sulfide bearing minerals. The Impact melts are distinguishable by the texture of the matrix is made up of silicates, enstatite in particular. There metal and sulfide assemblages. A meteorite that was are usually no oxides found, which supports the idea that impact melted will contain a texture of euhedral to these formed in very oxygen poor environments. The subhedral silicates, like enstatite, protruding into the metal enstatite chondrites in this study are type 3, meaning they or sulfides (figure 2). Some textures will look shattered are unmetamorphosed and not affected by fluids. (figure 2b). Meteorites that contain the mineral keilite are Studying enstatite chondrites will help us determine the PCA 91125 ALHA 77156 PCA 91444 PCA 91085 also an indicator of impact melts (figure 3). Keilite only evolution of their parent bodies which formed at the occurs in enstatite chondrite impact-melt rocks that cooled beginning of our solar system. -
Meteorite Collections: Sample List
Meteorite Collections: Sample List Institute of Meteoritics Department of Earth and Planetary Sciences University of New Mexico October 01, 2021 Institute of Meteoritics Meteorite Collection The IOM meteorite collection includes samples from approximately 600 different meteorites, representative of most meteorite types. The last printed copy of the collection's Catalog was published in 1990. We will no longer publish a printed catalog, but instead have produced this web-based Online Catalog, which presents the current catalog in searchable and downloadable forms. The database will be updated periodically. The date on the front page of this version of the catalog is the date that it was downloaded from the worldwide web. The catalog website is: Although we have made every effort to avoid inaccuracies, the database may still contain errors. Please contact the collection's Curator, Dr. Rhian Jones, ([email protected]) if you have any questions or comments. Cover photos: Top left: Thin section photomicrograph of the martian shergottite, Zagami (crossed nicols). Brightly colored crystals are pyroxene; black material is maskelynite (a form of plagioclase feldspar that has been rendered amorphous by high shock pressures). Photo is 1.5 mm across. (Photo by R. Jones.) Top right: The Pasamonte, New Mexico, eucrite (basalt). This individual stone is covered with shiny black fusion crust that formed as the stone fell through the earth's atmosphere. Photo is 8 cm across. (Photo by K. Nicols.) Bottom left: The Dora, New Mexico, pallasite. Orange crystals of olivine are set in a matrix of iron, nickel metal. Photo is 10 cm across. (Photo by K. -
Buseckite, (Fe,Zn,Mn)S, a New Mineral from the Zakłodzie Meteorite
American Mineralogist, Volume 97, pages 1226–1233, 2012 Buseckite, (Fe,Zn,Mn)S, a new mineral from the Zakłodzie meteorite CHI MA,* JOHN R. BECKETT, AND GEORGE R. ROSSMAN Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California 91125, U.S.A. ABSTRACT Buseckite (IMA 2011-070), (Fe,Zn,Mn)S, is the Fe-dominant analog of wurtzite, a new member of the wurtzite group discovered in Zakłodzie, and an ungrouped enstatite-rich achondrite. The type material occurs as single-crystal grains (4–20 µm in size) in contact with two or more of enstatite, plagioclase, troilite, tridymite, quartz, and sinoite. Low-Ni iron, martensitic iron, schreibersite, keilite, cristobalite, and graphite, which are also present in the type sample, are not observed to be in contact with buseckite. Buseckite is black under diffuse illumination and nearly opaque grayish brown in transmitted light. The mean chemical composition of buseckite, as determined by electron micro- probe analysis of the type material, is (wt%) S 35.84, Fe 28.68, Zn 23.54, Mn 10.04, Mg 1.18, sum 99.28, leading to an empirical formula calculated on the basis of 2 atoms of (Fe0.46Zn0.32Mn0.16Mg0.04 )∑0.99S1.01. Electron backscatter diffraction patterns of buseckite are a good match to that of synthetic 3 (Zn0.558Fe0.442)S with the P63mc structure, showing a = 3.8357, c = 6.3002 Å, V = 80.27 Å , and Z = 2. Buseckite is likely derived from the breakdown of high-temperature pyrrhotite to form troilite and buseckite following the solidification of sulfide-rich liquids produced during impact melting of an enstatite-rich rock.