Mineral Deposit Models for Northeast Asia
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An Evolutionary System of Mineralogy: Proposal for a Classification Of
1 1 02 November 2018—American Mineralogist—Revision 1 2 3 4 An evolutionary system of mineralogy: Proposal for a classification 5 of planetary materials based on natural kind clustering 6 7 ROBERT M. HAZEN1,* 8 1Geophysical Laboratory, Carnegie Institution for Science, 9 5251 Broad Branch Road NW, Washington, DC 20015, U. S. A. 10 11 ABSTRACT 12 Minerals reveal the nature of the co-evolving geosphere and biosphere through billions of years 13 of Earth history. Mineral classification systems have the potential to elucidate this rich 14 evolutionary story; however, the present mineral taxonomy, based as it is on idealized major 15 element chemistry and crystal structure, lacks a temporal aspect and thus cannot reflect planetary 16 evolution. A complementary evolutionary system of mineralogy based on the quantitative 17 recognition of “natural kind clustering” for a wide range of condensed planetary materials with 18 different paragenetic origins has the potential to amplify, though not supersede, the present 19 classification system. 20 21 _________________________________ 22 *E-mail: [email protected] 23 Keywords: philosophy of mineralogy; classification; mineral evolution; mineral ecology; data- 24 driven discovery; cluster analysis; natural kinds 2 25 INTRODUCTION 26 For more than 2000 years, the classification of natural objects and phenomena into “kinds” has 27 been a central pursuit of natural philosophers (Aristotle/Thompson 1910; Locke 1690; Linnaeus 28 1758). The modern mineral classification system, rooted in the chemical framework of James 29 Dwight Dana (1850), is based on unique combinations of idealized major element composition 30 and crystal structure (Strunz 1941; Palache et al. 1944, 1951; Liebau 1985; Mills et al. -
Network Analysis of Mineralogical Systems
American Mineralogist, Volume 102, pages 1588–1596, 2017 OUTLooKS IN EARTH AND PLANETARY MATERIALS k Network analysis of mineralogical systems SHAUNNA M. MORRISON1, CHAO LIU1, AHmeD ELEISH1,2, ANIRUDH PRABHU2, CONGRUI LI2, JOLYON RALPH3, ROBERT T. DOWNS4, JOSHUA J. GOLDEN4, PETER FOX2, DANIEL R. HUmmeR1,5, MICHAEL B. MEYER1, AND ROBERT M. HAZEN1,* 1Geophysical Laboratory, Carnegie Institution for Science, 5251 Broad Branch Road NW, Washington, D.C. 20015, U.S.A. 2Tetherless World Constellation, Department of Earth and Environmental Sciences, Rensselaer Polytechnic Institute, Troy, New York 12180, U.S.A. 3Mindat.org, 128 Mullards Close, Mitcham, Surrey, CR4 4FD, U.K. 4Department of Geosciences, University of Arizona, 1040 East 4th Street, Tucson, Arizona 85721-0077, U.S.A. 5Department of Geology, Southern Illinois University, Carbondale, Illinois 62901, U.S.A. ABSTRACT A fundamental goal of mineralogy and petrology is the deep understanding of mineral phase relation- ships and the consequent spatial and temporal patterns of mineral coexistence in rocks, ore bodies, sediments, meteorites, and other natural polycrystalline materials. The multi-dimensional chemical com- plexity of such mineral assemblages has traditionally led to experimental and theoretical consideration of 2-, 3-, or n-component systems that represent simplified approximations of natural systems. Network analysis provides a dynamic, quantitative, and predictive visualization framework for employing “big data” to explore complex and otherwise hidden higher-dimensional patterns of diversity and distribution in such mineral systems. We introduce and explore applications of mineral network analysis, in which mineral species are represented by nodes, while coexistence of minerals is indicated by lines between nodes. This approach provides a dynamic visualization platform for higher-dimensional analysis of phase relationships, because topologies of equilibrium phase assemblages and pathways of mineral reaction series are embedded within the networks. -
Persson Mines 0052N 11296.Pdf
THE GEOCHEMICAL AND MINERALOGICAL EVOLUTION OF THE MOUNT ROSA COMPLEX, EL PASO COUNTY, COLORADO, USA by Philip Persson A thesis submitted to the Faculty and Board of Trustees of the Colorado School of Mines in partial fulfillment of the requirements for the degree of Master of Science (Geology). Golden, Colorado Date ________________ Signed: ________________________ Philip Persson Signed: ________________________ Dr. Katharina Pfaff Thesis Advisor Golden, Colorado Date ________________ Signed: ________________________ Dr. M. Stephen Enders Professor and Interim Head Department of Geology and Geological Engineering ii ABSTRACT The ~1.08 Ga Pikes Peak Batholith is a type example of an anorogenic (A)-type granite and hosts numerous late-stage sodic and potassic plutons, including the peraluminous to peralkaline Mount Rosa Complex (MRC), located ~15 km west of the City of Colorado Springs in Central Colorado. The MRC is composed of Pikes Peak biotite granite, fayalite-bearing quartz syenite, granitic dikes, Mount Rosa Na-Fe amphibole granite, mafic dikes ranging from diabase to diorite, and numerous rare earth (REE) and other high field strength element (HFSE; e.g. Th, Zr, Nb) rich Niobium-Yttrrium-Fluorine (NYF)-type pegmatites. The aim of this study is to trace the magmatic evolution of the Mount Rosa Complex in order to understand the relationship between peraluminous and peralkaline rock units and concomitant HFSE enrichment and mineralization processes. Field work, petrography, SEM-based methods, whole rock geochemistry, and electron probe micro-analysis (EPMA) of micas was performed on all rock units to determine their textural, mineralogical and geochemical characteristics. Early peraluminous units such as the Pikes Peak biotite granite and fayalite-bearing quartz syenite contain annite-siderophyllite micas with high Fe/(Fe + Mg) ratios, and show relatively minor enrichments in REE and other HFSE compared to primitive mantle. -
Minor- and Trace-Element Composition of Trioctahedral Micas: a Review
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/249851431 Minor- and trace-element composition of trioctahedral micas: A review Article in Mineralogical Magazine · April 2001 DOI: 10.1180/002646101550244 CITATIONS READS 100 1,145 3 authors, including: H.-J. Förster Helmholtz-Zentrum Potsdam - Deutsches GeoForschungsZentrum GFZ 297 PUBLICATIONS 6,380 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Special Issue of journal Minerals on Accessory Minerals in Silicic Igneous Rocks View project Geochemistry of late-Variscan granites of the Erzgebirge-Vogtland metallogenic province View project All content following this page was uploaded by H.-J. Förster on 06 May 2014. The user has requested enhancement of the downloaded file. Mineralogical Magazine, April 2001, Vol. 65(2), pp. 249–276 Minor- and trace-element composition of trioctahedral micas: a review 1 2, 2 G. TISCHENDORF , H.-J. FO¨ RSTER * AND B. GOTTESMANN Bautzner Str. 16, 02763 Zittau, Germany GeoForschungsZentrum Potsdam, Telegrafenberg, 14473 Potsdam, Germany ABSTRACT More than 19,000 analytical data mainly from the literature were used to study statistically the distribution patterns of F and the oxides of minor and trace elements (Ti, Sn, Sc, V, Cr, Ga, Mn, Co, Ni, Zn, Sr, Ba, Rb, Cs) in trioctahedral micas of the system phlogopite-annite/siderophyllite- polylithionite (PASP), which is divided here into seven varieties, whose compositional ranges are defined by the parameter mgli (= octahedral Mg minus Li). Plots of trace-element contents vs. mgli reveal that the elements form distinct groups according to the configuration of their distribution patterns. -
Rubies and Sapphires from Snezhnoe, Tajikistan
FEATURE ARTICLES RUBIES AND SAPPHIRES FROM SNEZHNOE , T AJIKISTAN Elena S. Sorokina, Andrey K. Litvinenko, Wolfgang Hofmeister, Tobias Häger, Dorrit E. Jacob, and Zamoniddin Z. Nasriddinov Discovered during the late 1970s, the Snezhnoe ruby and sapphire deposit in Tajikistan was active until the collapse of the former Soviet Union in the early 1990s and the outbreak of regional conflicts. This marble-hosted occurrence has seen renewed interest, as it is a large and potentially productive deposit that has not been sufficiently studied. Testing of samples identified solid inclusions of margarite enriched with Na and Li (calcic ephesite or soda margarite). These are believed to be previously unreported for gem corundum. Allanite, muscovite, and fuchsite (chromium-bearing muscovite) were identified for the first time in ruby and sapphire from Snezhnoe. These and other inclusions such as zircon, rutile, K- feldspar, and Ca-Na-plagioclase could serve to distinguish them from stones mined elsewhere. Con - centrations of trace elements were typical for ruby and sapphire of the same formation type. The highest Cr concentrations were observed within the bright red marble-hosted rubies, and these values were very similar to those of the famous Burmese rubies from Mogok. orundum— -Al O —is a common, though net, scapolite, lazurite, and variscite (Litvinenko α 2 3 minor, component of many metamorphic and Barnov, 2010). The occurrence of ruby in the Crocks. Gem-quality varieties of ruby and sap - Pamirs was first suggested by the Soviet mineralo - phire occur in only a few primary metamorphic and magmatic rock types depleted in silica and enriched Figure 1. -
GCE2 Database Information
GCE2: TCS Geochemical/Environmental Database Database name (acronym): TCS Geochemical/Environmental Database (GCE) Database owner: Thermo-Calc Software AB Database version: 2.4 GCE2 is a database containing about 600 minerals. It is used in applications such as geochemistry, geophysics, hydro-metallurgy, aqueous chemistry and environmental chemistry. Included Elements (46) Ag Al Ar As Au B Ba Be Br C Ca Cd Cl Co Cr Cs Cu F Fe Ga Gd H Hg I K Li Mg Mn Mo N Na Ni O P Pb Rb S Se Si Sn Sr Ti U V W Zn Included Phases GCE2 contains critically assessed temperature-, pressure- and composition-dependent data for minerals (silicates, oxides, hydroxides, halides, carbonates, sulfides, sulfates, nitrates, phosphates, etc.). The Birch- Murnaghan model for the pressure dependence of EOS is used. The applicable temperatures range from 298.15 K to about 6000 K and pressures from 1 bar to 1000 kbar (100 GPa). The compounds are treated as either stoichiometric or solution phases. A metallic liquid solution phase is included, but currently there is no data for melt mixture phases with e.g., oxide/silicate/carbonate/sulfide/sulphate/... species (of neutral or charged forms). GCE2 List of Phases GCE2 is compatible with almost all other thermodynamic databases available from Thermo-Calc. Especially, when combined with the AQS database, GCE can be applied to investigate complex heterogeneous interactions among minerals, aqueous solutions and sub-critical H2O over a wide temperature - pressure - composition range. Assessed Systems All phases have been critically assessed and treated by appropriate thermodynamic models. www.thermocalc.com GCE2: TCS Geochemical/Environmental Database ǀ 2 of 27 Limits As in the spirit of the CALPHAD method, predictions can be made for multicomponent systems by extrapolation into multicomponent space of data critically evaluated and assessed based on binary, ternary and in some cases higher order systems. -
Contact Zone Mineralogy and Geochemistry of the Mt. Mica Pegmatite, Oxford County, Maine
University of New Orleans ScholarWorks@UNO University of New Orleans Theses and Dissertations Dissertations and Theses Spring 5-16-2014 Contact Zone Mineralogy and Geochemistry of the Mt. Mica Pegmatite, Oxford County, Maine Kimberly T. Clark University of New Orleans, [email protected] Follow this and additional works at: https://scholarworks.uno.edu/td Part of the Geochemistry Commons, and the Geology Commons Recommended Citation Clark, Kimberly T., "Contact Zone Mineralogy and Geochemistry of the Mt. Mica Pegmatite, Oxford County, Maine" (2014). University of New Orleans Theses and Dissertations. 1786. https://scholarworks.uno.edu/td/1786 This Thesis is protected by copyright and/or related rights. It has been brought to you by ScholarWorks@UNO with permission from the rights-holder(s). You are free to use this Thesis in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights- holder(s) directly, unless additional rights are indicated by a Creative Commons license in the record and/or on the work itself. This Thesis has been accepted for inclusion in University of New Orleans Theses and Dissertations by an authorized administrator of ScholarWorks@UNO. For more information, please contact [email protected]. Contact Zone Mineralogy and Geochemistry of the Mt. Mica Pegmatite, Oxford County, Maine A Thesis Submitted to the Graduate Faculty of the University of New Orleans in partial fulfillment of the requirements for the degree of Master of Science In Earth and Environmental Science By Kimberly T. Clark B.S. -
An In-Vitro Evaluation of the Capacity of Local Tanzanian Crude Clay and Ash Based Materials in Binding Aflatoxins in Solution
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 2 November 2018 doi:10.20944/preprints201811.0021.v1 Peer-reviewed version available at Toxins 2018, 10, 510; doi:10.3390/toxins10120510 An in-vitro evaluation of the capacity of local Tanzanian crude clay and ash based materials in binding aflatoxins in solution 1,3Ayo E. M; 2G. H. Laswai; 1A. Matemu; 1M. E. Kimanya* 1 The Nelson Mandela African Institution of Science and Technology, P.O. Box 447, Arusha. Tanzania E-mails: [email protected]; [email protected]: kimanya.martin@nm-aist 2 Sokoine University of Agriculture, P.O. Box 3004, Morogoro. Tanzania, E-mail: [email protected] 3 Institute of Rural Development Planning, P.O. Box 138, Dodoma, Tanzania, E-mail: [email protected] *The corresponding author, email: kimanya.martin@nm-aist Corresponding author: Prof Martin E. Kimanya (Associate Professor of Food safety and Nutrition Sciences) P.O. Box 447, Arusha. Tanzania; e-mail: [email protected] Abstract Aflatoxins in feeds cause great health hazards to animals and in advance, to human. Potential of crude clays designated AC, KC, CC and MC and ashes VA and RA were evaluated for their capacity to adsorb aflatoxins B1 (AFB1), B2 (AFB2), G1 (AFG1) and G2 (AFG2) relative to a commercial binder MycobinderR (Evonik Industries AG) using in-vitro technique. On average, CC, VA, KC, MC, AC, RA and MycobindR adsorbed 39.9%, 51.3%, 61.5%, 62.0%, 72.6%, 84.7% and 98.1% of the total aflatoxins in buffered solution, respectively. -
Studies in the Mica Group; Single Crystal Data on Phlogopites, Biotites and Manganophyllites A
STUDIES IN THE MICA GROUP; SINGLE CRYSTAL DATA ON PHLOGOPITES, BIOTITES AND MANGANOPHYLLITES A. A. LBvTNSoNAND E. Wu. Horwucu, Department oJ Mineralogy, The Ohio State [Inioersity, Columbus, Ohio, and. Department of Minerology, Uni.aersityoJ Michigan, Ann Arbor, Michigon. AssrnA.ct Weissenberg studies of about 250 specimens of phlogopite, biotite and manganophyllite, of which 63 have been chemically analyzed, indicate: (1) in phlogopites there is no dis- cernible relationship between structure and either composition or paragenesis; (2) in biotites there is no relationship between structure and composition, but geologic environ- ment may be a factor in determining the polymorphic type; (3) the optic plane of all 2-layer polymorphs is normal to (010), as is also the case for the biotite variety, anomitel and (4) lJayer polymorphs nearly always have the optic plane parallel with (010), which corresponds with the orientation of the biotite variety, meroxene. IxrnooucuoN Systematic variations between composition and the various poly- morphs in the muscovite-lepidolite series have been demonstrated by Levinson (1953). On the basis of these results it seemeddesirable to investigate the biotite-phlogopite seriesin a similar manner in the hope of gaining insight into causes of the complex polymorphism known to exist in these micas. The only other Weissenbergstudy of these micas known to the writers is in the work of Hendricks and Jefferson (1939), predominantly on unanalyzed specimens. We have obtained over 60 analyzed specimensof biotite, phlogopite and manganophyllite (which we consider as manganoan phlogopite), most of which have been describedby several investigators. In addition we have studied a suite of approximately 200 unanalyzed biotites and phlogopites from geologically well-studied occurrences. -
Clay Minerals
American Minetralogist, Volume 65, pages 1-7, 1980 Summary of recommendations of AIPEA nomenclature committee on clay minerals S. W. BAILEY, CHAIRMAN1 Department of Geology and Geophysics University of Wisconsin-Madison Madi~on, Wisconsin 53706 Introduction This summary of the recommendations made to Because of their small particle sizes and v~riable date by the international nomenclature committees degrees of crystal perfection, it is not surprisi4g that has been prepared in order to achieve wider dissemi- clay minerals proved extremely difficult to character- nation of the decisions reached and to aid clay scien- ize adequately prior to the development of ~odem tists in the correct usage of clay nomenclature. Some analytical techniques. Problems in charactetization of the material in the present summary has been led quite naturally to problems in nomenclatute, un- taken from an earlier summary by Bailey et al. doubtedly more so than for the macroscopic~ more (1971a). crystalline minerals. The popular adoption ~ the early 1950s of the X-ray powder diffractometer for Classification . clay studies helped to solve some of the probl ms of Agreement was reached early in the international identification. Improvements in electron micro copy, discussions that a sound nomenclatur~ is necessarily electron diffraction and oblique texture electr ;n dif- based on a satisfactory classification scheme. For this fraction, infrared and DT A equipment, the de elop- reason, the earliest and most extensive efforts of the ment of nuclear and isotope technology, of high- several national nomenclature committees have been speed electronic computers, of Mossbauer spec rome- expended on classification schemes. Existing schemes ters, and most recently of the electron micr probe were collated and discussed (see Brown, 1955, Mac- and scanning electron microscope all have ai ed in kenzie, 1959, and Pedro, 1967, for examples), sym- the accumulation of factual information on clays. -
A Specific Gravity Index for Minerats
A SPECIFICGRAVITY INDEX FOR MINERATS c. A. MURSKyI ern R. M. THOMPSON, Un'fuersityof Bri.ti,sh Col,umb,in,Voncouver, Canad,a This work was undertaken in order to provide a practical, and as far as possible,a complete list of specific gravities of minerals. An accurate speciflc cravity determination can usually be made quickly and this information when combined with other physical properties commonly leads to rapid mineral identification. Early complete but now outdated specific gravity lists are those of Miers given in his mineralogy textbook (1902),and Spencer(M,i,n. Mag.,2!, pp. 382-865,I}ZZ). A more recent list by Hurlbut (Dana's Manuatr of M,i,neral,ogy,LgE2) is incomplete and others are limited to rock forming minerals,Trdger (Tabel,l,enntr-optischen Best'i,mmungd,er geste,i,nsb.ildend,en M,ineral,e, 1952) and Morey (Encycto- ped,iaof Cherni,cal,Technol,ogy, Vol. 12, 19b4). In his mineral identification tables, smith (rd,entifi,cati,onand. qual,itatioe cherai,cal,anal,ys'i,s of mineral,s,second edition, New york, 19bB) groups minerals on the basis of specificgravity but in each of the twelve groups the minerals are listed in order of decreasinghardness. The present work should not be regarded as an index of all known minerals as the specificgravities of many minerals are unknown or known only approximately and are omitted from the current list. The list, in order of increasing specific gravity, includes all minerals without regard to other physical properties or to chemical composition. The designation I or II after the name indicates that the mineral falls in the classesof minerals describedin Dana Systemof M'ineralogyEdition 7, volume I (Native elements, sulphides, oxides, etc.) or II (Halides, carbonates, etc.) (L944 and 1951). -
Mineralogy and Mineral Chemistry of Rare-Metal Pegmatites at Abu Rusheid Granitic Gneisses, South Eastern Desert, Egypt
GEOLOGIJA 54/2, 205–222, Ljubljana 2011 doi:10.5474/geologija.2011.016 Mineralogy and mineral chemistry of rare-metal pegmatites at Abu Rusheid granitic gneisses, South Eastern Desert, Egypt Mohamed F. RASLAN & Mohamed A. ALI Nuclear Materials Authority, P.O. Box 530, El Maadi, Cairo, Egypt; e-mail: raslangains�hotmail.com Prejeto / Received 28. 2. 2011; Sprejeto / Accepted 22. 6. 2011 Key words: Hf-zircon, uranyl silicate minerals, Nb-Ta minerals, uraninite, Abu Rushied pegmatite, South Eastern Desert, Egypt Abstract The Abu Rushied area, situated in the South Eastern Desert of Egypt is a distinctive occurrence of economically important rare-metal mineralization where the host rocks are represented by granitic gneisses. Correspondingly, mineralogical and geochemical investigation of pegmatites pockets scattered within Abu Rusheid granitic gneisses revealed the presence of Hf-zircon, ferrocolumbite and uranyl silicate minerals (uranophane and kasolite). Elec- tron microprobe analyses revealed the presence of Nb-Ta multioxide minerals (ishikawaite, uranopyrochlore, and fergusonite), uraninite, thorite and cassiterite as numerous inclusions in the recorded Hf-zircon and ferrocolum- bite minerals. Abu Rusheid pegmatites are found as small and large bodies that occur as simple and complex (zoned) pegma- tites. Abu Rusheid rare-metal pegmatites occur as steeply dipping bodies of variable size, ranging from 1 to 5 m in width and 10 to 50 m in length. The zoned pegmatites are composed of wall zone of coarser granitic gneisses, intermediated zone of K-feldspar and pocket of mica (muscovite and biotite), and core of quartz and pocket of mica with lenses of rare metals. The zircon is of bipyramidal to typical octahedral form and short prisms.