Description and Origin of Carbonate Minerals in the Upper and Lower Cherty Members of the Biwabik Formation, Minnesota Leslie R

Total Page:16

File Type:pdf, Size:1020Kb

Description and Origin of Carbonate Minerals in the Upper and Lower Cherty Members of the Biwabik Formation, Minnesota Leslie R University of North Dakota UND Scholarly Commons Theses and Dissertations Theses, Dissertations, and Senior Projects 1973 Description and origin of carbonate minerals in the upper and lower cherty members of the Biwabik Formation, Minnesota Leslie R. Honeyman University of North Dakota Follow this and additional works at: https://commons.und.edu/theses Part of the Geology Commons Recommended Citation Honeyman, Leslie R., "Description and origin of carbonate minerals in the upper and lower cherty members of the Biwabik Formation, Minnesota" (1973). Theses and Dissertations. 142. https://commons.und.edu/theses/142 This Thesis is brought to you for free and open access by the Theses, Dissertations, and Senior Projects at UND Scholarly Commons. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of UND Scholarly Commons. For more information, please contact [email protected]. DESCRIPTION AND ORIGIN OF CARBONATE NEIERALS IN THE UPPER. AND LOWER CHER.TY ?•IF1'-fBERS OF THE :BIWABIK FORE,\.TION, HI:l:\1{ESCTA Leslie R. Honeyman, Master of Science The University of North Dakota, 1973 Faculty Advisor: Professor Frank Karner This study was done for the Erie Mining Company after periodic problems with the quality of pellets from taconite of the Biwabik Fonna­ tion had been linked to the presence of carbonate minerals. The carbon­ ates fouad in the cherty members of the Precambrian Biwabik Formation are predominantly side~ite, ankerite, and calcite. Siderite is the only primary carbonate mineral and occurs in three forms: microgran­ ular, granular (oolitic), and crystalline aggregates (recrystallized). Ankerite is a secondary mineral occurring as crystalline aggregates and alteration rims on granular siderite. Calcite is found only in fractures and fault zones. Siderite formed from the original precip­ itate and early in the diagenetic history of the rock. The alteration of siderite to fine-grained, euhedral magnetite appears to be the major part of the pellet-quality problem at Erie. The fine-grained magnetite causes small amounts of siderite to be incorporated with magnetite in the magnetic separation process. This siderite breaks down when the pellet is roasted and carbon dioxide is given off causing the pellet to disintegrate. Ankerite formed in two periods: the ankerite rims on siderite granules formed early in epigenesis and the crystalline ankerite formed much later, Calcite formed late in the epigenetic l history of the formation. It appears that the carbonates of the cherty members of the Biwabik :b'ormation can be used as indicators of an envi- ronment of deposition having reducing conditions and as indicators of the extent of metamorphism caused by the intrusion of the Duluth Gabbro. 2 DESCRIPTION Al\l) ORIGIN OF CAIGONATE HINEPALS I:~ THE UPPER AND LOWER CHZRTY MEHBERS OF TEE BIWABIK FORM.AT IO?:;, l'IINNESOTA by Leslie R. Honeyman Bachelor of Philosophy, University of North Dakota, 1969 A Thesis Submitted to the Graduate Faculty of the University of North Dakota in partial fulfillment of the requirements for the degree of Master of Science Grand lorks, North Dakota August 1973 This thesis submitted by Leslie R. Honeyman in partial fulfill­ ment of the requirements for the Degree of Master of Science from the University of North Dakota is hereby approved by the Faculty Advisory Committee under whom the work has been done. /- ( Chainnan) · \ ' '· ii DESCRIPTION Ai).:'D ORIGIN OF CARBONATE r-IINER...\.LS IN THE UPPER Al\'1J LOWER CHERTY }I™BERS OF THE BIWABIK Degree -----------------------------------Master of Science In presenting this thesis in partial fulfillment of the requirements for a graduate degree from the University of North Dakota, I agree that the Library of this University shall make it freely r2vailable for inspection. I further agree that permission for extensive copying for scholarly purposes may be granted by the professor who supervised my thesis work or, in his absence,·by the Chairman of the Depart­ ment or the Dean of the Graduate School. It is understood that any copying or publication or othe:c use of this thesis or part thereof for financial gain shall not be allowed with­ out my written permission. It is also understood that due recognition shall be given to me and to the University of North Dakota in any scholarly use which may be made of any material in my thesis. Date iii ACKNOWI ... EDGHE1"'T S The three members of my committee, particularly my com.rnittee chairman Dr. Frank Karner, are gratefully acknowledged for their con­ structive criticism and suggestions during the course of this work. The other two members are ffrs. Walter L. Moore and Lee Clayton. Erie Mining Company, Hoyt Lakes, Minnesota supplied funds for field support, laboratory analysis, and thin sections. Wayne Tuttle, Forrest Boyee, and Joe Evers of the Erie Mining Company supplied immeasurable help and assistance while I was on the Erie property. iv T.ATJLE CF COl.TTENTS ACK?WWLEDGHm!TS iv LIST OF TABLES vi LIST OF FIGURES vii ABSTRACT ix INTRODUCTIQ1(l 1 STR..4.TIGRAPHY 4 General Lower Cherty Hember Lower Slaty 11er:iber Upper Cherty Member Upper Slaty Hember METHODS • 14 CARBONATE PETROGP..APHY • 2S Basic Definiticns Siderite Ankerite Calcite DIFFERENCE IN CONCENTRA.TION OF CARBONATE MINERALS • • • • • • • 42 Lower Cherty Member Upper Cherty Member INTERPRETATIONS OF CHANGES IN CARBONATE CONCE!:.'TRATION AND OCCURRENCE • • • • • • • • • • • • • • • • • • • 48 Siderite Ankerite Calcite CONCLUSIONS 52 APPE'rlillIX. Weight Per,::entage for Sample Interval 57 REFERENCES . .. .. 64 V LIST OF TABLES Table Page 1. Comparison of Hineral Abundances Obtained by X-ray and Point-Count Methods. · 23 2. Precision of X-ray De.termination of Peak Intensities 24 3~ Weight Per~entage for Sample Interval. • • • • • • • • • 58 vi LIST OJ? FI·:;:aRES 1. Location and Geologic Map of Study Area Modified from Erie (1967) ..... 3 2. Geologic Cohu-nn for the Eastern Hesabi Range. from Erie (1967) ........... 6 3. Photograph of Interbedded Carbonate and Magnetite­ Rich Chert in Outcrop .••..••••. 15 4. Locations of Drill Hole and Pit Samples from Areal; Area 6; Area 3; and Area 2-West • • . • 18 5. Photomicrographs Showing the Occurrences of Siderite as (A) Hicrogranular Siderite; (B) Granular Siderite with Hicrogranular Side.rite Cement; (C) Granular Siderite with Chert Cement; and (D) Crystalline Aggregates of Siderite (Recrystallized) . • . •••••. 28 ,,. o. Photomicrographs Showing the Alteration or Replacements of Siderite to (A) Recrystallized Siderite; (B) Magnetite; (C) Ankerite and Hagnetite; (D) Ankerite; (E) Minnesotaite; (F) Stilpncmelane; ((;) Quartz; and (R) Stilpnomelane and Magnetite 31 7. Photomicrographs Showing the Oc.currences of Ankerite as (A) talline Rhombs; and (B) Alteration Rims o~ Siderite Granules. • • • ••• 37 8. Photomicrograph Showing Ankerite Altered to or Replaced by Magnetite •... 39 9. Photomicrograph Shot,ing a Calcite Vein •• 41 10. Triangular Diagrams Showing Vertical and Lateral Changes in the Concentrations of Siderite, Ankerite, and Calcite in the U, T, S, and R Layers of the Lower Cherty Member 44 11. Triangular Diagrams Showing the Vertical and Lateral Changes in the Concentrations of Siderite, Ankerite, and Calcite in the L, K', K, and J Layers of the Upper Cherty Member ••..•...•.• 47 vii 12. The Precipitation and Deposition of Carbonate }faterial in the Biwabik Fon,,.ation (I·fodified from DiElC:Qth and Chauvel, 1973) .. 55 viii This study was done. for the Erie Hining Company after periodic problems with the quality of pellets from taconit2 of the Biwabik Forrr.~- tion had been linked to the presence of carbonate minerals. The. carbon- ates found in the cherty members of the Precambrian Biwabik Formation are predominantly siderite, ankerite, and calcite. Siderite is the only primary carbonate mineral and occurs in three forms: nicrogran­ ular, granular (oolitic), and crystalline aggregates (recrystallized). Ankerite is a secondary mineral occurring as crystalline aggregates and alteration rims on granular siderite. Calcite is found only in fractures and fault zones. (siderite formed from the original precip­ itate and early in the diagenetic history of the rock. The alteration of siderite to fine-grained, euhedral magnetite appears to be the major part of the pellet-quality problem at Erie. The fine-grained magnetite causes small amounts of siderite to be incorporated with magnetite in the magnetic separation process. This siderite breaks down when the pellet is roasted and carbon dioxide is given of£ causing the pellet to disintegrate. Ankerite formed in two periods: the ankerite rims on siderite granules formed early in epigenesis and the crystalline ankerite formed much later. Calcite formed late in the epigenetic history of the formation. It appears that the carbonates of the cherty members of the Biwabik Formation can be used as indicators of an environment of deposition having reducing conditions and as indicators of the extent of metamorphism caused by the intrusion of the Duluth Gabbro. ix INTRODUCTION This study was done for the Erie. Hir1ing after periodic problems with the quality of pellets from taconite of the Biwabik. For-- matio.::1 h2.d been linked to the presenc2. of carbon.:cte minerals. The purpose was to determine the of carbonate minerals present, the relationships of the carbonate minerals to each other, and ultimately to the environ.,.~ent of deposition of the taconite. The area of study is the Erie Mining Company property, extend­ ing from the western edge of Area 1, just north of Aurora, 1'1innesota, to the eastern edge of Area 8, along the western edge of Birch Lake, where the Duluth Gabbro Complex transects the Biwabik Formation (Figure 1). Vertical and lateral differences in carbonate mineralogy were studied in four geologic zones within each of the two cherty members of the Biwabik. Carbonate minerals have been altered to various sili­ cates, oxides, and other carbonate minerals; the difference in carbon­ ate minerals is critical in its effect on pellet quality of the high- vollli~e taconite reining operations.
Recommended publications
  • 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.
    [Show full text]
  • 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
    [Show full text]
  • 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
    [Show full text]
  • Depositional Setting of Algoma-Type Banded Iron Formation Blandine Gourcerol, P Thurston, D Kontak, O Côté-Mantha, J Biczok
    Depositional Setting of Algoma-type Banded Iron Formation Blandine Gourcerol, P Thurston, D Kontak, O Côté-Mantha, J Biczok To cite this version: Blandine Gourcerol, P Thurston, D Kontak, O Côté-Mantha, J Biczok. Depositional Setting of Algoma-type Banded Iron Formation. Precambrian Research, Elsevier, 2016. hal-02283951 HAL Id: hal-02283951 https://hal-brgm.archives-ouvertes.fr/hal-02283951 Submitted on 11 Sep 2019 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. Accepted Manuscript Depositional Setting of Algoma-type Banded Iron Formation B. Gourcerol, P.C. Thurston, D.J. Kontak, O. Côté-Mantha, J. Biczok PII: S0301-9268(16)30108-5 DOI: http://dx.doi.org/10.1016/j.precamres.2016.04.019 Reference: PRECAM 4501 To appear in: Precambrian Research Received Date: 26 September 2015 Revised Date: 21 January 2016 Accepted Date: 30 April 2016 Please cite this article as: B. Gourcerol, P.C. Thurston, D.J. Kontak, O. Côté-Mantha, J. Biczok, Depositional Setting of Algoma-type Banded Iron Formation, Precambrian Research (2016), doi: http://dx.doi.org/10.1016/j.precamres. 2016.04.019 This is a PDF file of an unedited manuscript that has been accepted for publication.
    [Show full text]
  • Infrare D Transmission Spectra of Carbonate Minerals
    Infrare d Transmission Spectra of Carbonate Mineral s THE NATURAL HISTORY MUSEUM Infrare d Transmission Spectra of Carbonate Mineral s G. C. Jones Department of Mineralogy The Natural History Museum London, UK and B. Jackson Department of Geology Royal Museum of Scotland Edinburgh, UK A collaborative project of The Natural History Museum and National Museums of Scotland E3 SPRINGER-SCIENCE+BUSINESS MEDIA, B.V. Firs t editio n 1 993 © 1993 Springer Science+Business Media Dordrecht Originally published by Chapman & Hall in 1993 Softcover reprint of the hardcover 1st edition 1993 Typese t at the Natura l Histor y Museu m ISBN 978-94-010-4940-5 ISBN 978-94-011-2120-0 (eBook) DOI 10.1007/978-94-011-2120-0 Apar t fro m any fair dealin g for the purpose s of researc h or privat e study , or criticis m or review , as permitte d unde r the UK Copyrigh t Design s and Patent s Act , 1988, thi s publicatio n may not be reproduced , stored , or transmitted , in any for m or by any means , withou t the prio r permissio n in writin g of the publishers , or in the case of reprographi c reproductio n onl y in accordanc e wit h the term s of the licence s issue d by the Copyrigh t Licensin g Agenc y in the UK, or in accordanc e wit h the term s of licence s issue d by the appropriat e Reproductio n Right s Organizatio n outsid e the UK. Enquirie s concernin g reproductio n outsid e the term s state d here shoul d be sent to the publisher s at the Londo n addres s printe d on thi s page.
    [Show full text]
  • Spectral Evolution Alteration Zone Mapping
    spectral evolution Alteration Zone Mapping As geologists explore a region, oreXpress spectrometers with EZ-ID software can pro- vide detailed data by measuring reflectance from outcrops, chips, or drill core. Using an oreXpress, EZ-ID and a laptop or tablet, they can detect alteration minerals and chemi- cal/crystalline variations that are not immediately apparent to even the most experi- enced and well trained human eye. With the oreXpress geologists can identify: Micas—muscovite-paragonite, biotite, phlogopite Chlorites—variations in iron-magnesium chlorite, epidote Amphiboles—tremolite, hornblende, actinolite Sulfates—jarosite, gypsum Clays—illite, illite-smectite, kaolinite, dickite oreXpress and oreXpress Carbonates—calcite, dolomite, ankerite, siderite Platinum spectrometers are used to Tourmaline—Fe-tourmaline, tourmaline better understand and map mineral alteration zones in the field. Using EZ-ID with the USGS and SpecMIN libraries, a geologist can quickly identify an alteration mineral that may not be readily identifiable by sight, matching an unknown sample against a known spectral library. With EZ-ID the geologist can select specific spectral regions to fine-tune the matching process for a more precise ID. If the geolo- gist wants to look at a particular absorption feature, the geologist can highlight that or other features and EZ-ID provides new matches. The USGS library contains 466 spectra for 226 minerals; SpecMIN has 1528 spectra for 500 minerals. By ordering EZ-ID with both libraries, a geologist has access to a wide range of match possibilities for exploration projects in iron, gold, copper, silver, nickel, uranium, and rare earths. EZ-ID software identifies minerals EZ-ID works right from the DARWin SP Data Acquisition software included with all in real-time by matching your SPECTRAL EVOLUTION spectrometers and spectroradiometers.
    [Show full text]
  • Characterisation of Carbonate Minerals from Hyperspectral TIR Scanning Using Features at 14 000 and 11 300 Nm
    Australian Journal of Earth Sciences An International Geoscience Journal of the Geological Society of Australia ISSN: 0812-0099 (Print) 1440-0952 (Online) Journal homepage: http://www.tandfonline.com/loi/taje20 Characterisation of carbonate minerals from hyperspectral TIR scanning using features at 14 000 and 11 300 nm D. Green & M. Schodlok To cite this article: D. Green & M. Schodlok (2016): Characterisation of carbonate minerals from hyperspectral TIR scanning using features at 14 000 and 11 300 nm, Australian Journal of Earth Sciences, DOI: 10.1080/08120099.2016.1225601 To link to this article: http://dx.doi.org/10.1080/08120099.2016.1225601 Published online: 13 Nov 2016. Submit your article to this journal Article views: 13 View related articles View Crossmark data Full Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=taje20 Download by: [Bundesstalt Fuer Geowissenschaften] Date: 21 November 2016, At: 02:06 AUSTRALIAN JOURNAL OF EARTH SCIENCES, 2016 http://dx.doi.org/10.1080/08120099.2016.1225601 Characterisation of carbonate minerals from hyperspectral TIR scanning using features at 14 000 and 11 300 nm D. Greena and M. Schodlokb aMineral Resources Tasmania, Department of State Growth, Hobart, Australia; bBundesanstalt fur€ Geowissenschaften und Rohstoffe (Federal Institute for Geosciences and Natural Resources), Hannover, Germany ABSTRACT ARTICLE HISTORY Rapid characterisation of carbonate phases in hyperspectral reflectance spectra acquired from drill Received 11 February 2016 core material has important implications for mineral exploration and resource modelling. Major Accepted 9 August 2016 infrared active features of carbonates lie in the thermal region around 6500 nm, 11 300 nm and KEYWORDS 14 000 nm, with the latter two features being most useful for differentiating mineral species.
    [Show full text]
  • STABLE ISOTOPES of HYDROTHERMAL CARBONATE MINERALS in the BUTTE PORPHYRY-LODE DEPOSITS, MONTANA Ryan Stevenson Montana Tech of the University of Montana
    Montana Tech Library Digital Commons @ Montana Tech Graduate Theses & Non-Theses Student Scholarship Summer 2015 STABLE ISOTOPES OF HYDROTHERMAL CARBONATE MINERALS IN THE BUTTE PORPHYRY-LODE DEPOSITS, MONTANA Ryan Stevenson Montana Tech of the University of Montana Follow this and additional works at: http://digitalcommons.mtech.edu/grad_rsch Part of the Biogeochemistry Commons, Geology Commons, and the Geophysics and Seismology Commons Recommended Citation Stevenson, Ryan, "STABLE ISOTOPES OF HYDROTHERMAL CARBONATE MINERALS IN THE BUTTE PORPHYRY-LODE DEPOSITS, MONTANA" (2015). Graduate Theses & Non-Theses. 44. http://digitalcommons.mtech.edu/grad_rsch/44 This Thesis is brought to you for free and open access by the Student Scholarship at Digital Commons @ Montana Tech. It has been accepted for inclusion in Graduate Theses & Non-Theses by an authorized administrator of Digital Commons @ Montana Tech. For more information, please contact [email protected]. STABLE ISOTOPES OF HYDROTHERMAL CARBONATE MINERALS IN THE BUTTE PORPHYRY-LODE DEPOSITS, MONTANA by Ryan Stevenson A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Geosciences Montana Tech 2015 ii Abstract The stable isotopic compositions of over 90 hydrothermal carbonate minerals in the Butte porphyry-lode system were analyzed. These samples came from the underground workings as well as the active Continental Pit area. Most material came from polymetallic “Main Stage” veins which post-date the porphyry Cu-Mo mineralization of Butte. Some samples from late calcite-stellerite veins were also included in the study. Rhodochrosite 13C and 18O values range from -8.3 to -2.9‰ (average of -6.7±1.0‰) and -1.8 to 12.8‰ (average of 3.6 ±3.4‰) respectively, while calcite 13C and 18O values range from -9.0 to -2.6‰ (average of -5.4 ± 1.5‰) and -4.4 to 12.3‰ (average of 6.2±2.8‰) respectively.
    [Show full text]
  • High-Pressure Structural Study of Dolomite and Ankerite
    American Mineralogist, Volume 77, pages412-421, 1992 High-pressure structural study of dolomite and ankerite NlNcv L. Ross Deparrment of Geological Sciences,University CollegeLondon, Gower Street,London WCIE 68T, U.K. Rrcn.q.noJ. Rrnnnn Mineral PhysicsInstitute and Department of Earth and SpaceSciences, State University of New York, StonyBrook, New York 11794,U.S.A. Ansrucr Structural parametershave been refined using X-ray intensity data for a stoichiometric dolomite singlecrystal at room pressureand at 1.50,2.90,3.70, and 4.69 GPa; and for a single crystal of a ferroan dolomite with approximately 70 molo/oCaFe(COr)' at room pressureand at 1.90,2.97, and 4.0 GPa. The principal structuralchange with increasing pressureis compression of the CaOu and (Mg,Fe)Ouoctahedra. The CO, group remains essentiallyinvariant throughout the pressurerange studied. The effect of the polyhedral compression is reflected in the anisotropic compression of the unit-cell parameters. In both dolomite and ankerite, c is approximately three times as compressibleas a. In addition to displaying similar axial compressibilities,dolomite and ankerite display similar bond compressibilitiesand bulk moduli. The isothermal bulk modulus of dolomite determined from cell volume compressiondata, assumingthe pressurederivative is 4, is 94 GPa,and that of ankerite is 9l GPa. The polyhedralbulk moduli of CaO. and (Mg,Fe)Ou are also similar, with CaOu being slightly more compressiblethan (Mg,Fe)Ou'The latter has a greater compressibility than generally observed in other oxides and silicates. The distortion of the octahedra, though already small, decreasesslightly with pressure.No phasechange was observedin either compound throughout the pressurerange studied.
    [Show full text]
  • List of Abbreviations
    List of Abbreviations Ab albite Cbz chabazite Fa fayalite Acm acmite Cc chalcocite Fac ferroactinolite Act actinolite Ccl chrysocolla Fcp ferrocarpholite Adr andradite Ccn cancrinite Fed ferroedenite Agt aegirine-augite Ccp chalcopyrite Flt fluorite Ak akermanite Cel celadonite Fo forsterite Alm almandine Cen clinoenstatite Fpa ferropargasite Aln allanite Cfs clinoferrosilite Fs ferrosilite ( ortho) Als aluminosilicate Chl chlorite Fst fassite Am amphibole Chn chondrodite Fts ferrotscher- An anorthite Chr chromite makite And andalusite Chu clinohumite Gbs gibbsite Anh anhydrite Cld chloritoid Ged gedrite Ank ankerite Cls celestite Gh gehlenite Anl analcite Cp carpholite Gln glaucophane Ann annite Cpx Ca clinopyroxene Glt glauconite Ant anatase Crd cordierite Gn galena Ap apatite ern carnegieite Gp gypsum Apo apophyllite Crn corundum Gr graphite Apy arsenopyrite Crs cristroballite Grs grossular Arf arfvedsonite Cs coesite Grt garnet Arg aragonite Cst cassiterite Gru grunerite Atg antigorite Ctl chrysotile Gt goethite Ath anthophyllite Cum cummingtonite Hbl hornblende Aug augite Cv covellite He hercynite Ax axinite Czo clinozoisite Hd hedenbergite Bhm boehmite Dg diginite Hem hematite Bn bornite Di diopside Hl halite Brc brucite Dia diamond Hs hastingsite Brk brookite Dol dolomite Hu humite Brl beryl Drv dravite Hul heulandite Brt barite Dsp diaspore Hyn haiiyne Bst bustamite Eck eckermannite Ill illite Bt biotite Ed edenite Ilm ilmenite Cal calcite Elb elbaite Jd jadeite Cam Ca clinoamphi- En enstatite ( ortho) Jh johannsenite bole Ep epidote
    [Show full text]
  • Mineral Index
    Mineral Index Abhurite T.73, T.355 Anandite-Zlvl, T.116, T.455 Actinolite T.115, T.475 Anandite-20r T.116, T.45S Adamite T.73,T.405, T.60S Ancylite-(Ce) T.74,T.35S Adelite T.115, T.40S Andalusite (VoU, T.52,T.22S), T.27S, T.60S Aegirine T.73, T.30S Andesine (VoU, T.58, T.22S), T.41S Aenigmatite T.115, T.46S Andorite T.74, T.31S Aerugite (VoU, T.64, T.22S), T.34S Andradite T.74, T.36S Agrellite T.115, T.47S Andremeyerite T.116, T.41S Aikinite T.73,T.27S, T.60S Andrewsite T.116, T.465 Akatoreite T.73, T.54S, T.615 Angelellite T.74,T.59S Akermanite T.73, T.33S Ankerite T.74,T.305 Aktashite T.73, T.36S Annite T.146, T.44S Albite T.73,T.30S, T.60S Anorthite T.74,T.415 Aleksite T.73, T.35S Anorthoclase T.74,T.30S, T.60S Alforsite T.73, T.325 Anthoinite T.74, T.31S Allactite T.73, T.38S Anthophyllite T.74, T.47S, T.61S Allanite-(Ce) T.146, T.51S Antigorite T.74,T.375, 60S Allanite-(La) T.115, T.44S Antlerite T.74, T.32S, T.60S Allanite-(Y) T.146, T.51S Apatite T.75, T.32S, T.60S Alleghanyite T.73, T.36S Aphthitalite T.75,T.42S, T.60 Allophane T.115, T.59S Apuanite T.75,T.34S Alluaudite T.115, T.45S Archerite T.75,T.31S Almandine T.73, T.36S Arctite T.146, T.53S Alstonite T.73,T.315 Arcubisite T.75, T.31S Althausite T.73,T.40S Ardaite T.75,T.39S Alumino-barroisite T.166, T.57S Ardennite T.166, T.55S Alumino-ferra-hornblende T.166, T.57S Arfvedsonite T.146, T.55S, T.61S Alumino-katophorite T.166, T.57S Argentojarosite T.116, T.45S Alumino-magnesio-hornblende T.159,T.555 Argentotennantite T.75,T.47S Alumino-taramite T.166, T.57S Argyrodite (VoU,
    [Show full text]
  • 39015003286252.Pdf
    raY a ... 3 4 _' J t+..,+1 /y s t O'C4 LOOM lescE NATUML- 010SIS OF THE TUNGSTEN EPOSITS OF THE UNITED STATES 4 Itoag tn February,. 1936 CONTENTS INTRODUCTION .. .. .............................. 1 LOCATION AND DISTRIBUTION ............................... 2 TYPES OF DEPOSITS OF COMMERCIAL TUNGSTEN ORE...........lO1 Pyrometasomatic deposits ................. ........ 10 Hypothermal deposits .................. S......0.12 Mesothermal deposits.......................... .12 Epithermal deposits...............................13 General features .... ............ .. .. .. 16 Non-Commercial Deposits .. .. ... .. ... ... .. .. .. ... .. 19 Segregation deposits .. .. ... .. .. ... .,.. .. .,.. .19 General features . ..... ....... .. .. .. 19 General features ......... ... .. .. .. .. .".". ."20 Associated minerals.. .. .". .. ."..".."""" 21 Commercial Deposits . .... * . .. .29.. Pyrometasomatic or contact-metamorphic deposits... .22 Location of deposits ............. "..... ... "". 23 Intrusive rocks. .. .23 CONTENTS (concluded) Sedimnrta~ry rocks. ... ......9" . 0 . .24 Process of contacte-metamorphism.0........ .... 24 Size and form of the deposits ................. 26 Zones of metamorphism.................. ".O".S" .26 Progression of the contact-metamorphism. ..... .27 General features and classification..g09.....28 Associated minerals............... "." " " ..... "29. Outcrop of tungsten veins.9......0.. 00"03 Downward extent of tungsten ve ins...........3 Gelaeenral.fatur.. .. .. ... .. .. ..... .. ........ 39 General features.......9. .
    [Show full text]