Phase Relations in Cordierite-Garnet-Bearing
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
CORDIERITE-GARNET GNEISS and ASSOCIATED MICRO- CLINE-RICH PEGMATITE at STURBRIDGE, I,{ASSA- CHUSETTS and UNION, CONNECTICUTI Fnor B.Cnrbn, [
THE AMERICAN MINERALOGIST, VOL 47, IVLY AUGUST, 1962 CORDIERITE-GARNET GNEISS AND ASSOCIATED MICRO- CLINE-RICH PEGMATITE AT STURBRIDGE, I,{ASSA- CHUSETTS AND UNION, CONNECTICUTI Fnor B.cnrBn, [/. S. GeologicalSurttey, Washington,D. C. Aesrnacr Gneiss of argillaceous composition at Sturbridge, Massachusetts, and at Union, Connecticut, 10 miles to the south, consists of the assemblagebiotite-cordierite-garnet- magnetite-microcline-quartz-plagioclase-sillimanite. The conclusion is made that this assemblagedoes not violate the phase rule. The cordierite contains 32 mole per cent of Fe- end member, the biotite is aluminous and its ratio MgO: (MgOf I'eO) is 0.54, and the gar- net is alm6e5 pyr26.agro2.espe1.2.Lenses of microcline-quartz pegmatite are intimately as- sociated with the gneissl some are concordant, others cut acrossthe foliation and banding of the gneiss. The pegmatites also contain small amounts of biotite, cordierite, garnet, graphite, plagioclase, and sillimanite; each mineral is similar in optical properties to the corresponding one in the gneiss. It is suggestedthat muscovite was a former constituent of the gneiss at a lower grade of metamorphism, and that it decomposedwith increasing metamorphism, and reacted with quartz to form siliimanite in situ and at lerst part of the microcline of the gneiss and pegmatites These rocks are compared with similar rocks of Fennoscandia and Canada. INtnouucrroN Cordierite-garnet-sillimanitegneisses that contain microcline-quartz pegmatiteare found in Sturbridge,Massachusetts, and Union, Connecti- cut. The locality (Fig. 1) at Sturbridgeis on the south sideof the \{assa- chusettsTurnpike at the overpassof the New Boston Road; this is about 1 mile west of the interchangeof Route 15 with the Turnpike. -
Hypersthene Syenite and Related Rocks of the Blue Ridge Region, Virginia1
BULLETIN OF THE GEOLOGICAL SOCIETY OF AMERICA V o l. 27, pp. 193-234 June 1, 1916 HYPERSTHENE SYENITE AND RELATED ROCKS OF THE BLUE RIDGE REGION, VIRGINIA1 BY THOMAS L. WATSON AND JUSTUS H. CLINE (Presented before the Society December 29, 191k) CONTENTS Page Introduction.................................................................................................................. 194 Previous geologic work............................................................................................. 196 Quartz-bearing hypersthene-andesine syenite...................................................... 197 Distribution.......................................................................................................... 197 Megascopic character......................................................................................... 198 Microscopic character........................................................................................ 199 Chemical composition and classification...................................................... 202 Comparison with quartz monzonite.............................................................. 204 Origin and application of name............................................................. 204 Chemical composition................................................................................ 205 Comparison with akerite.................................................................................. 206 Comparison with syenite (andesine anorthosite) of Nelson County, Virginia............................................................................................................. -
Phase Equilibria and Thermodynamic Properties of Minerals in the Beo
American Mineralogist, Volwne 71, pages 277-300, 1986 Phaseequilibria and thermodynamic properties of mineralsin the BeO-AlrO3-SiO2-H2O(BASH) system,with petrologicapplications Mlnx D. B.qnroN Department of Earth and SpaceSciences, University of California, Los Angeles,Los Angeles,California 90024 Ansrru,cr The phase relations and thermodynamic properties of behoite (Be(OH)r), bertrandite (BeoSirOr(OH)J, beryl (BerAlrSiuO,r),bromellite (BeO), chrysoberyl (BeAl,Oo), euclase (BeAlSiOo(OH)),and phenakite (BerSiOo)have been quantitatively evaluatedfrom a com- bination of new phase-equilibrium, solubility, calorimetric, and volumetric measurements and with data from the literature. The resulting thermodynamic model is consistentwith natural low-variance assemblagesand can be used to interpret many beryllium-mineral occurTences. Reversedhigh-pressure solid-media experimentslocated the positions of four reactions: BerAlrSiuO,,: BeAlrOo * BerSiOo+ 5SiO, (dry) 20BeAlSiOo(OH): 3BerAlrsi6or8+ TBeAlrOo+ 2BerSiOn+ l0HrO 4BeAlSiOo(OH)+ 2SiOr: BerAlrSiuO,,+ BeAlrOo+ 2H2O BerAlrSiuO,,+ 2AlrSiOs : 3BeAlrOa + 8SiO, (water saturated). Aqueous silica concentrationswere determined by reversedexperiments at I kbar for the following sevenreactions: 2BeO + H4SiO4: BerSiOo+ 2H2O 4BeO + 2HoSiOo: BeoSirO'(OH),+ 3HrO BeAlrOo* BerSiOo+ 5H4Sio4: Be3AlrSiuOr8+ loHro 3BeAlrOo+ 8H4SiO4: BerAlrSiuOrs+ 2AlrSiO5+ l6HrO 3BerSiOo+ 2AlrSiO5+ 7H4SiO4: 2BerAlrSiuOr8+ l4H2o aBeAlsioloH) + Bersio4 + 7H4sio4:2BerAlrsiuors + 14Hro 2BeAlrOo+ BerSiOo+ 3H4SiOo: 4BeAlSiOr(OH)+ 4HrO. -
Cordierite-Bearing Gneisses in the West-Central Adirondack Highlands
Trip A-6 CORDIERITE-BEARING GNEISSES IN THE WEST -CENTRAL ADIRONDACK HIGHLANDS Frank P. Florence Science Division, Jefferson Community College, Watertown, NY, USA 13601 [email protected] Robert S. Darling Department of Geology, SUNY College at Cortland, Cortland, NY, USA 13045 Phillip R. Whitney New York State Geological Survey (ret.), New York State Museum, Albany, NY, USA 12230 Gregory W. Lester Department of Geological Sciences and Geological Engineering, Queen's University, Kingston, Ontario, CANADA K7L 3N6 INTRODUCTION Cordierite-bearing gneiss is uncommon in the Adirondack Highlands. To date, it is has been described from three locations, one near the village ofInlet (Seal, 1986; Whitney et aI, 2002) and two along the Moose River further to the west (Darling et aI, 2004). All of these cordierite occurrences are located in the west-central Adirondacks, a region characterized by somewhat lower metamorphic pressures as compared to the rest of the Adirondack Highlands (Florence et aI, 1995; Darling et aI, 2004). In the Fulton Chain of Lakes area of the west-central Adirondack Highlands, a heterogeneous unit of metasedimentary rocks, including cordierite-bearing gneisses, forms the core of a major NE to ENE trending synform. Cordierite appears in an assortment of mineral assemblages, including one containing the uncommon borosilicate, prismatine, the boron-rich end-member ofkornerupine (Grew et ai., 1996). The assemblage cordierite + orthopyroxene is also present, the first recognized occurrence of this mineral pair in the Adirondack Highlands (Darling et aI, 2004). This field trip includes stops at four outcrops containing cordierite in mineral assemblages that are characteristic of granulite facies metamorphism in aluminous rocks. -
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 -
Geochemistry of the Catheart Mountain Porphyry Copper Deposit, Maine
Maine Geological S urvey Studies in Maine Geology: Volume 4 1989 Geochemistry of the Catheart Mountain Porphyry Copper Deposit, Maine Robert A. Ayuso U.S. Geological Survey Reston, Virginia 22092 ABSTRACT The Ordovician Catheart Mountain pluton is the best example ofa porphyry copper system in the New England Appalachians. It intrudes the Ordovician Attean quartz monzonite in the Proterozoic Chain Lakes massif. The pluton consists of equigranular granodiorite intruded by porphyritic dikes of granite and granodiorite which contain up to 4% sulfides (pyrite, chalcopyrite, and molybdenite). The equigranular host rocks and the porphyritic dikes are generally chemically similar, showing scattered compositional variations which reflect changes imposed on the pluton during crystallization and hydrothermal alteration. Most rocks are hydrated, containing high C02 and high S. The most intensely altered parts of the pluton are potassic (up to 6.9 wt % KiO) and highly mineralized, especially with Cu (up to 3900 ppm), but also with Mo (up to 320 ppm). The host granodiorite and porphyritic dikes are depleted in Ca, Na, Fe2+ and Sr as a function of increasing Cu; the sulfide-rich rocks are enriched in Rb and they have high Fe3+/Fe2+, K/Na, and Rb/Sr values. Abundances and ratios of the highly-charged cations (e.g. Zr, Hf, Ta, and Th) in the Catheart Mountain pluton resemble those in the Devonian granodiorites in the northern Maine plutonic belt. Abundances and ratios of the highly-charged cations in the Sally Mountain pluton, a nearby body also containing Cu and Mo mineralization, differ significantly from those in the Catheart Mountain pluton suggesting that the two plutons are not comagmatic. -
52. Iron-Rich Cordierite Structurally Close to Indialite by Miyoji SAMBONSUGI Geological Institute, Faculty of Arts And. Science
190 [Vol. 33, 52. Iron-rich Cordierite Structurally Close to Indialite By Miyoji SAMBONSUGI GeologicalInstitute, Faculty of Arts and. Sciences,Fukushima University (Comm.by S. TsuBOI,M.J.A., April 1.2, 1957) Introduction In the course of his geological investigation of the Abukuma plateau, northeast Japan, the writer's attention was drawn to numerous pegmatites intruding the granitic and gneissic rocks which form the foundation of this district. In 1950 the writer found a peculiar mineral from one of the above-mentioned pegmatites, at Sugama. From its appearance the mineral was first identified as scapolite by the writer (Sambonsugi, 1953), but after further observations it has become clear that the mineral belongs to an iron-rich variety of cordierite, and that it is structurally close to indialite, hexagonal polymorph of cordierite, first found by Miyashiro and Iiyama (1954) from the fused sediment in the Bakaro coalfield, India. Miyashir0 et al. (1955) suspected that a structural gradation may exist between the hexagonal lattice of in- dialite and the orthorhombic lattice of cordierite, viz, that there may be some varieties of cordierite structurally close to indialite, though all then known show marked structural difference from indialite. The mineral found by the writer from the Sugama pegmatite is the first example of cordierite structurally close to indialite. It is the purpose of this paper to describe the mode of occurrence, the optical properties, and the chemical composition of the mineral. Recent- ly, the optical properties and the unit cell dimensions of the mineral were studied by T. Iiyama (1956). X-ray and thermal studies of the mineral were carried out by Miyashiro (1957). -
The Surface Reactions of Silicate Minerals
RESEARCH BULLETIN 614 SEPTEMBER, 1956 UNIVERSITY OF MISSOURI COLLEGE OF AGRICULTURE AGRICULTURAL EXPERIMENT STATION J. H. Longwell, Director The Surface Reactions Of Silicate Minerals PART II. REACTIONS OF FELDSPAR SURFACES WITH SALT SOLUTIONS. V. E. NASH AND C. E. MARSHALL (Publication authorized September 5, 1956) COLUMBIA, MISSOURI TABLE OF CONTENTS Introduction .......... .. 3 The Interaction of Albite with Salt Solutions . .. 4 The Interaction of Anorthite with Salt Solutions ........ .. 7 Relative Effectiveness of Ammonium Chloride and Magnesium Chloride on the Release of Sodium from Albite . .. 9 Surface Interaction of Albite with Salt Solutions in Methanol . .. 13 Experiments on Cationic Fixation ............................... 16 Detailed Exchange and Activity Studies with Individual Feldspars .......... .. 19 Procedure .. .. 20 Microcline . .. 21 Albite .................................................... 22 Oligoclase . .. 23 Andesine . .. 24 Labradori te . .. 25 Bytownite ................................................. 25 Anorthite . .. 27 Discussion ........ .. 28 Summary ..................................................... 35 References .. .. 36 Most of the experimental material of this and the preceding Research Bulletin is taken from the Ph.D. Thesis of Victor Nash, University of Missouri, June 1955. The experiments on cation fixation were carried our with the aid of a research grant from the Potash Rock Company of America, Lithonia, Georgia, for which the authors wish to record their appreciation. The work was part of Department of Soils Research Project No.6, entitled, "Heavy Clays." The Surface Reactions of Silicate Minerals PART II. REACTIONS OF FELDSPAR SURFACES WITH SALT SOLUTIONS. v. E. NASH AND C. E. MARSHALL INTRODUCTION The review of literature cited in Part I of this series indicates that little is known of the interaction of feldspar surfaces with salt solutions. The work of Breazeale and Magistad (1) clearly demonstrated that ex change reactions between potassium and calcium occur in the case of or thoclase surfaces. -
Fluid Inclusions Confirm Authenticity of Tibetan Andesine Date
GEMOLOGY Fluid Inclusions Confirm Authenticity of Tibetan Andesine Can Tibetan andesine now be certified? By Adolf Peretti1, Willy Bieri1, Kathrin Hametner2 and Detlef Günther2 with Richard W. Hughes and Ahmadjan Abduriyim Introduction Untreated copper-bearing feldspar of a rich red color is found in nature, but gem-quality pieces are scarce. For decades the major occurrence has been in Oregon (USA), but gem-quality red feld- spar also occurs in Japan (Furuya & Milisenda, 2009) and elsewhere. Beginning in 2002, gem-quality red plagioclase feldspar en- tered world gem markets. The source was originally stated as the Congo and later morphed into Tibet. By 2007, suspicions that such stones were the result of a treatment were widespread. These suspicions were confirmed in early 2008 (Furuya, 2008), when the treatment was revealed as one of copper diffusion into otherwise lightly-colored plagioclase. This was confirmed by laboratory experiments which replicated the treatment (Emmett & Douthit, 2009). Still, the question remained. Was there a genuine red feldspar mine in Tibet? If so, how would one separate such stones from the treated material? This question challenged the gemological community, resulting in several expeditions to the alleged Tibet- an localities for sample collection and subsequent testing. Figure 2. Copper-bearing red collected by Abduriyim from Yu Lin Gu and view into the valley. (Photos: Ahmadjan Abduriyim) The first of these forays was in 2008 to Bainang, southeast of Shigatse. A group led by Ahmadjan Abduriyim collected numer- ous samples and found the deposit to be credible. However, two subsequent visits (to two widely separated deposits, one of which was adjacent to Bainang) suggested copper-bearing an- desine occurrences in Tibet were being “salted” (Fontaine et al., 2010; Wang et al., 2010). -
Geologic Section of the Black Range at Kingston, New Mexico
BULLETIN 33 Geologic Section of the Black Range at Kingston, New Mexico BY FREDERICK J. KUELLMER Structure and stratigraphy of the Black Range, detailed petrology of igneous rocks, and general guides to ore exploration 1954 STATE BUREAU OF MINES AND MINERAL RESOURCES NEW MEXICO INSTITUTE OF MINING & TECHNOLOGY CAMPUS STATION SOCORRO, NEW MEXICO NEW MEXICO INSTITUTE OF MINING & TECHNOLOGY E. J. Workman, President STATE BUREAU OF MINES AND MINERAL RESOURCES Eugene Callaghan, Director THE REGENTS MEMBERS EX OFFICIO The Honorable Edwin L. Mechem ..............................Governor of New Mexico Tom Wiley ................................................ Superintendent of Public Instruction APPOINTED MEMBERS Robert W. Botts .............................................................................. Albuquerque Holm O. Bursum, Jr ................................................................................ Socorro Thomas M. Cramer ...............................................................................Carlsbad Frank C. DiLuzio .............................................................................Los Alamos A. A. Kemnitz ...........................................................................................Hobbs Contents Page ABSTRACT ......................................................... …………………………………… 1 INTRODUCTION ........................................................................................................3 ACKNOWLEDGMENTS .............................................................................................4 -
Mineralogy and Origin of the Titanium
MINERALOGY AND ORIGIN OF THE TITANIUM DEPOSIT AT PLUMA HIDALGO, OAXACA, MEXICO by EDWIN G. PAULSON S. B., Massachusetts Institute of Technology (1961) SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE at the MASSACHUSETTS INSTITUTE OF TECHNOLOGY May 18, 1962 Signature of At r . Depardnent of loggand Geophysics, May 18, 1962 Certified by Thesis Supervisor Ab Accepted by ...... Chairman, Departmental Committee on Graduate Students M Abstract Mineralogy and Origin of the Titanium Deposit at Pluma Hidalgo, Oaxaca, Mexico by Edwin G. Paulson "Submitted to the Department of Geology and Geophysics on May 18, 1962 in partial fulfillment of the requirements for the degree of Master of Science." The Pluma Hidalgo titanium deposits are located in the southern part of the State of Oaxaca, Mexico, in an area noted for its rugged terrain, dense vegetation and high rainfall. Little is known of the general and structural geology of the region. The country rocks in the area are a series of gneisses containing quartz, feldspar, and ferromagnesians as the dominant minerals. These gneisses bear some resemblance to granulites as described in the literature. Titanium minerals, ilmenite and rutile, occur as disseminated crystals in the country rock, which seems to grade into more massive and large replacement bodies, in places controlled by faulting and fracturing. Propylitization is the main type of alteration. The mineralogy of the area is considered in some detail. It is remarkably similar to that found at the Nelson County, Virginia, titanium deposits. The main minerals are oligoclase - andesine antiperthite, oligoclase- andesine, microcline, quartz, augite, amphibole, chlorite, sericite, clinozoi- site, ilmenite, rutile, and apatite. -
Ab Initio Calculations of Elastic Constants of Plagioclase Feldspars
UC Berkeley UC Berkeley Previously Published Works Title Ab initio calculations of elastic constants of plagioclase feldspars Permalink https://escholarship.org/uc/item/9fg3d711 Journal American Mineralogist, 99(11-12) ISSN 0003-004X Authors Kaercher, P Militzer, B Wenk, HR Publication Date 2014-11-01 DOI 10.2138/am-2014-4796 Peer reviewed eScholarship.org Powered by the California Digital Library University of California American Mineralogist, Volume 99, pages 2344–2352, 2014 Ab initio calculations of elastic constants of plagioclase feldspars PAMELA KAERCHER1,*, BURKHARD MILITZER1,2 AND HANS-RUDOLF WENK1 1Department of Earth and Planetary Science, University of California, Berkeley, California 94720, U.S.A. 2Department of Astronomy, University of California, Berkeley, California 94720, U.S.A. ABSTRACT Plagioclase feldspars comprise a large portion of the Earth’s crust and are very anisotropic, mak- ing accurate knowledge of their elastic properties important for understanding the crust’s anisotropic seismic signature. However, except for albite, existing elastic constants for plagioclase feldspars are derived from measurements that cannot resolve the triclinic symmetry. We calculate elastic constants for plagioclase end-members albite NaAlSi3O8 and anorthite CaAl2Si2O8 and intermediate andesine/ labradorite NaCaAl3Si5O16 using density functional theory to compare with and improve existing elastic constants and to study trends in elasticity with changing composition. We obtain elastic con- stants similar to measured elastic constants and find that anisotropy decreases with anorthite content. Keywords: Plagioclase feldspars, elastic constants, ab initio calculations, seismic anisotropy INTRODUCTION and taken into account. Plagioclase feldspars are one of the most important rock- Further uncertainty is introduced when elastic constants are forming minerals, comprising roughly 40% of the Earth’s crust.