MAINE PEGMATITE MINES and PROSPECTS and ASSOCIATED MINERALS
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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. -
The I\,Iagnetic Separation of Soi'ie Alluvial I,Iinerals in I'ialaya*
THE AMERICAN MINERAI,OGIST, VOL. 41, JULY AUGUST, 1959 THE I\,IAGNETIC SEPARATION OF SOI'IE ALLUVIAL I,IINERALS IN I'IALAYA* B. H. FnNrant, Minerals Eramination Diaision, GeologicalSurttey D epartment, F'ederotion of M al,aya. Assrnlcr This paper presents the results of a seriesof magnetic separationswhich have been in- vestigated {or a number of minerals occurring in X{alayan alluvial concentrates.The pur- pose of the investigations was to establish,by the isolation of individual mineral species,a reproducible and reliable method for the identification and quantitative estimation of minerals in alluvial concentrates examined by the Geological Survey in Malaya In par- ticular was sought the isolation of columbite from ubiquitous ilmenite. All the separations were made on the small, highly sensitive Frantz Isodynamic Model L-1 laboratory separa- tor, The minerals which have been successfully separated include ailanite, anatase, andalu- site (and chiastolite), arsenopyrite, brookite, cassiterite,columbite, epidote, gahnite, garnet (pink), ilmenite, manganeseoxide (51.6/e Mn), monazite, pyrite, rutile, scheelite,siderite, staurolite, thorite, topaz, tourmaline, uranoan monazite, wolframite, xenotime, and zircon. PnocBpunp When using an inclined feed, the Frantz Isodynamic separator (see Figs. 1(A) & (B)) hasthree inherent variables. These are the field strengLh (current used),the sideslope, and the forward slope. 5;6s $lope wdrd 511)Pe (A) (B) Irc. 1. Diagrammatic representation of side slope and forward slope. The field strength is increasedby means of a rheostat which raises the current from zero in stagesof 0.05 amps. to 1.4 amps. Early in the investigationsit was decidedthat stepsof 0.1 amp. would be sufficiently gradual. -
Summer 2015 Newsletter
Maine Appalachian Trail Land Trust Summer 2015 Newsletter Summer highlights inside • REPI Challenge Grant • Great Maine Outdoor Weekend Hike • Board Member Profile • Project Update • Community Events • And more! Baxter Peak, Katahdin REPI Challenge Grant Awarded The Maine Appalachian Trail Land Trust is currently a partnership that will help ensure necessary training conditions partnering with The Trust for Public Land (TPL) on a for the Navy while also protecting wildlife habitat and working number of conservation projects in the High Peaks area forests that support local jobs.” of the Appalachian Trail in Western Maine. We are pleased to announce that TPL has secured an additional Maine Appalachian Trail Land Trust Awarded $2 million in funding by winning a REPI Challenge grant Davis Conservation Foundation Grant from the Department of Defense’s Readiness and Environmental Protection Integration program. Portland, ME (August 7, 2015) – The Davis Conservation Foundation has awarded a grant of $12,000 to the Maine The funds will be used to restrict development of nearly Appalachian Trail Land Trust to support our work on the 10,000 acres around the military Survival, Evasion, Redington Forest project. The funds will allow the land trust to protect land along Maine’s Appalachian Trail via the Resistance and Escape school in western Maine, by the acquisition of a conservation easement over the project purchase of conservation easements over lands around the base. Maine A.T. Land Trust will be holding a area. These much-needed funds will help defray the costs involved in the easement acquisition process – legal work, conservation easement over Redington Forest and will GIS needs, personnel, stewardship and other associated be working closely with TPL on additional projects. -
Pyrophyllite Solid Solutions in the System A|,O,-S|O,-H,O
American Minerulogist, Volume 59, pages 254-260, 1974 PyrophylliteSolid Solutions in the SystemA|,O,-S|O,-H,O Pnrr,rp E. RoseNnenc D ep art ment ol G eolo gy, 14as hing ton Stat e U nio er sity, P ullman, 14as hington 99 I 6 3 Abstract Pyrophyllite solid solutions have been synthesized in the system Al,O'-SiOr-H,O between 400' and 565'C at 2 kbar from a variety of starting materials using sealed gold tubes and conventional hydrothermal techniques. The duration of experiments was 3-9 weeks. Products were characterized by X-ray measurementsand by infrared spectroscopy. Appreciably larger basal spacings were observed for pyrophyllite synthesized from gels than for natural pyrophyllite; small amounts of quartz were present in these samples. Basal spacings of pyrophyllite synthesized from mixtures of kaolinite and quartz approach but do not equal those of natural pyrophyllite. Rehydroxylation of dehydroxylated pyrophyllite under hydrothermal conditions suggests that enlargement of basal spacings cannot be due to dehydroxylation. Substitution of the type Al"* + H* : Sia* is proposed to explain the observed variations. The coupled substitution of Al3* and (OH)- for Sin*and O- results in expanded basal spacingsdue largely to the formation of OH on the basal surface and in increased thermal stability due to the formation of H-bonds between oxygens in adjacent silica sheets.Analyses of natural pyrophyllite also suggest limited substitution of this type. Failure to recognize these substitutions in synthetic samples accounts, in part, for dis- crepancies in the reported thermal stability of pyrophyllite. Phase characterization, often lack- ing, is essentialin experimentalstudies of mineral stabilities. -
INCLUSIONS in AQUAMARINE from AMBATOFOTSIKELY, MADAGASCAR Fabrice Danet, Marie Schoor, Jean-Claude Boulliard, Daniel R
NEW Danet G&G Fall 2012_Layout 1 9/27/12 11:31 AM Page 205 RAPID COMMUNICATIONS INCLUSIONS IN AQUAMARINE FROM AMBATOFOTSIKELY, MADAGASCAR Fabrice Danet, Marie Schoor, Jean-Claude Boulliard, Daniel R. Neuville, Olivier Beyssac, and Vincent Bourgoin grams of translucent to transparent beryl were pro- duced, as well as several tonnes of opaque material In January 2012, aquamarine crystals containing for industrial use. While only a very small percentage interesting inclusions were extracted from the Am- was suitable for faceting, several hundred aqua- batofotsikely area northwest of Antsirabe, Mada- marines in the 1–35 ct range have been cut. In April gascar. These specimens displayed various types 2012, one of the authors (FD) traveled to the locality of eye-visible and microscopic inclusions, and and obtained representative samples. some had an unusual form. Raman microspec- troscopy identified reddish brown plate lets as Location and Geologic Setting. The workings are lo- hematite, while ilmenite was found as black cated less than 1 km north of Ambatofotsikely (a village platelets, black needles, and distinctive dark gray now locally known as Ambatofotsy Carole), 22 km dendrites. Similar inclusions are known in beryl north-northwest of Ankazomiriotra, and 74 km north- from Brazil, India, Mozambique, and Sri Lanka. west of Antsirabe. The deposit is centered at coordinates 19°27.662¢S, 46°27.450¢E, at an elevation of 1,010 m. The site is accessed by a paved road (RN 34) from ining activity near the central Malagasy village Antsirabe to a point 16 km west of Ankazomiriotra. of Ambatofotsikely was first documented nearly From there, a trail extends 15 km to Ambatofotsikely. -
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. -
Weathering of Ilmenite from Granite and Chlorite Schist in the Georgia Piedmont
American Mineralogist, Volume 87, pages 1616–1625, 2002 Weathering of ilmenite from granite and chlorite schist in the Georgia Piedmont PAUL A. SCHROEDER,* JOHN J. LE GOLVAN, AND MICHAEL F. RODEN Department of Geology, University of Georgia, Athens, Georgia 30602-2501, U.S.A. ABSTRACT Ilmenite grains from weathering profiles developed on granite and ultramafic chlorite schist in the Georgia Piedmont were studied for evidence of morphological and chemical alteration. Ilmenite- rich concentrates from the fine sand (90–150 mm) component were studied to test the assumption that there is no difference between ilmenite in the parent rock and that in colluvium delivered to primary drainage systems. Ilmenite grains in the granite profile are rounded to subhedral, and commonly contain hematite exsolution blebs. Dissolution pits are observed along the boundaries of the exsolution blebs, with goethite occurring as an alteration product. Ilmenite grains in the schist profile occur as fractured anhedral grains with uncommon lamellae of rutile. Grain fractures are filled with goethite and he- matite, particularly in the B-horizon. Ilmenite from the granite profile is Mn rich (7–15 mol% MnTiO3), whereas ilmenite from the schist profile contains only 1–2 mol% MnTiO3 and up to 8 mol% MgTiO3. Two populations of grains develop in both profiles. Grains with abundant exsolution blebs and fractures alter through a proposed two-step reaction mechanism. It is proposed that il- menite first undergoes a solid-state transformation to pseudorutile via an anodic oxidation mecha- nism. Oxidized Fe and Mn diffuse from the structure and precipitate as goethite and MnO2. Pseudorutile is ephemeral and undergoes incongruent dissolution to form anatase, hematite, and goethite. -
The Pyrophyllite Deposits of North Carolina
North Carolina Department of Conservation and Development Wade H. Phillips, Director BULLETIN NUMBER 37 THE PYROPHYLLITE DEPOSITS OF NORTH CAROLINA With A MORE DETAILED ACCOUNT OF THE GEOLOGY OF THE DEEP RIVER REGION By JASPER L. STUCKEY, Ph. D. RALEIGH 19 28 MEMBERS OF THE BOARD OF CONSERVATION AND DEVELOPMENT Governor A. W. McLean, Chairman, ex offtcio Raleigh S. Wade Marr __._ Raleigh B. B. Gossett Charlotte Jas. G. K. McClure, Jr Asheville Fred I. Sutton ~ _: .. Kinston E. D. Cranford . Asheboro R. Bruce Btheridge Manteo Santford Martin . ; Winston-Salem E. S. Askew Merry Hill J. Q. Gilket Marion F. S. Worthy Washington George L. Hampton Canton Frank H. Stedman Fayetteville Wade H. Phillips, Director, Raleigh LETTER OF TRANSMITTAL Raleigh, N. C, August 1, 1928. To His Excellency, Hon. A. W. McLean, Governor of North Carolina. Sir:—I herewith submit for publication as Bulletin No. 37 of the publications of the North Carolina Department of Con servation and Development a report on The Pyrophyllite De posits of North Carolina, which has been prepared by Dr. Jasper L. Stuckey, former State Geologist. This is the first complete report on the pyrophyllite deposits of this State and will, therefore, be of great interest to those who desire infor mation on such material. Yours respectfully, Wade H. Phillips, Director, North Carolina Department of Conservation and Development. AUTHOR'S FOREWORD This report was begun as a special investigation of the geology and pyrophyllite deposits of the Deep River Region, and accord ingly a detailed geologic map of that region was prepared. As the work progressed, other pyrophyllite deposits were found outside the area mapped. -
Porphyry Deposits
PORPHYRY DEPOSITS W.D. SINCLAIR Geological Survey of Canada, 601 Booth St., Ottawa, Ontario, K1A 0E8 E-mail: [email protected] Definition Au (±Ag, Cu, Mo) Mo (±W, Sn) Porphyry deposits are large, low- to medium-grade W-Mo (±Bi, Sn) deposits in which primary (hypogene) ore minerals are dom- Sn (±W, Mo, Ag, Bi, Cu, Zn, In) inantly structurally controlled and which are spatially and Sn-Ag (±W, Cu, Zn, Mo, Bi) genetically related to felsic to intermediate porphyritic intru- Ag (±Au, Zn, Pb) sions (Kirkham, 1972). The large size and structural control (e.g., veins, vein sets, stockworks, fractures, 'crackled zones' For deposits with currently subeconomic grades and and breccia pipes) serve to distinguish porphyry deposits tonnages, subtypes are based on probable coproduct and from a variety of deposits that may be peripherally associat- byproduct metals, assuming that the deposits were econom- ed, including skarns, high-temperature mantos, breccia ic. pipes, peripheral mesothermal veins, and epithermal pre- Geographical Distribution cious-metal deposits. Secondary minerals may be developed in supergene-enriched zones in porphyry Cu deposits by weathering of primary sulphides. Such zones typically have Porphyry deposits occur throughout the world in a series significantly higher Cu grades, thereby enhancing the poten- of extensive, relatively narrow, linear metallogenic tial for economic exploitation. provinces (Fig. 1). They are predominantly associated with The following subtypes of porphyry deposits are Mesozoic to Cenozoic orogenic belts in western North and defined according to the metals that are essential to the eco- South America and around the western margin of the Pacific nomics of the deposit (metals that are byproducts or poten- Basin, particularly within the South East Asian Archipelago. -
Geologic Evolution of Trail Ridge Eolian Heavy-Mineral Sand and Underlying Peat, Northern Florida
Georgia Southern University Digital Commons@Georgia Southern Geology and Geography Faculty Publications Geology and Geography, Department of 1989 Geologic Evolution of Trail Ridge Eolian Heavy-Mineral Sand and Underlying Peat, Northern Florida Eric Force U.S. Geological Survey Fredrick J. Rich Georgia Southern University, [email protected] Follow this and additional works at: https://digitalcommons.georgiasouthern.edu/geo-facpubs Part of the Geography Commons, and the Geology Commons Recommended Citation Force, Eric, Fredrick J. Rich. 1989. "Geologic Evolution of Trail Ridge Eolian Heavy-Mineral Sand and Underlying Peat, Northern Florida." U.S. Geological Survey Professional Paper 1499: 1-23 Washington, DC: United States Government Printing Office. source: https://pubs.er.usgs.gov/publication/pp1499 https://digitalcommons.georgiasouthern.edu/geo-facpubs/117 This article is brought to you for free and open access by the Geology and Geography, Department of at Digital Commons@Georgia Southern. It has been accepted for inclusion in Geology and Geography Faculty Publications by an authorized administrator of Digital Commons@Georgia Southern. For more information, please contact [email protected]. Geologic Evolution of Trail Ridge EoMmn Peat, Northern Florida AVAILABILITY OF BOOKS AND MAPS OF THE U.S. GEOLOGICAL SURVEY Instructions on ordering publications of the U.S. Geological Survey, along with prices of the last offerings, are given in the cur- rent-year issues of the monthly catalog "New Publications of the U.S. Geological Survey." Prices of available U.S. Geological Sur- vey publications released prior to the current year are listed in the most recent annual "Price and Availability List." Publications that are listed in various U.S. -
Geology of the Buckfield and Dixfield Quadrangles in Northwestern Maine
University of New Hampshire University of New Hampshire Scholars' Repository New England Intercollegiate Geological NEIGC Trips Excursion Collection 1-1-1965 Geology of the Buckfield and Dixfield Quadrangles in Northwestern Maine Warner, Jeffrey Pankiwskyj, Kost A. Follow this and additional works at: https://scholars.unh.edu/neigc_trips Recommended Citation Warner, Jeffrey and Pankiwskyj, Kost A., "Geology of the Buckfield and Dixfield Quadrangles in Northwestern Maine" (1965). NEIGC Trips. 78. https://scholars.unh.edu/neigc_trips/78 This Text is brought to you for free and open access by the New England Intercollegiate Geological Excursion Collection at University of New Hampshire Scholars' Repository. It has been accepted for inclusion in NEIGC Trips by an authorized administrator of University of New Hampshire Scholars' Repository. For more information, please contact [email protected]. TRIP K Geology of the Buckfield and Dixfield Quadrangles in Northwestern Maine Leaders: Jeffrey Warner, Harvard University and Maine Geological Survey Kost A. Pankiwskyj, University of Hawaii and Maine Geological Survey INTRODUCTION This trip will study the Silurian and Devonian rocks on the south east limb of a major northeast plunging syncline. All the rocks seen are in the sillimanite and staurolite zones of metamorphism. The stratigraphic nomenclature developed by Billings and his co-workers in New Hampshire was originally used in this area. However after detailed mapping by Fisher (1962), Guidotti (1965), Pankiwskyj (1964), and Warner (in preparation) in respectively the Bethel, Bryant Fond, Dixfield, and Buckfield Quadrangles, a new set of stratigraphic names was developed. Although these names are not yet official, we use them here as a matter of convenience. -
Structures of the 2:1 Layers of Pyrophyllite and Talc
Clays and Clay Minerals, Vol. 60, No. 6, 574–587, 2012. STRUCTURES OF THE 2:1 LAYERS OF PYROPHYLLITE AND TALC 1 2 1, 3 V ICTOR A. DRITS ,STEPHEN G UGGENHEIM ,BELLA B. ZVIAGINA *, AND T OSHIHIRO K OGURE 1 Geological Institute of the Russian Academy of Science, Pyzhevsky per. 7, 119017 Moscow, Russia 2 Department of Earth and Environmental Sciences, University of Illinois at Chicago, Chicago, IL 60607, USA 3 Department of Earth and Planetary Science, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan Abstract—To determine the relationships between the symmetry of the overall pyrophyllite and talc structure and the symmetry of individual layers, the geometry and symmetry of each 2:1 layer of pyrophyllite and talc were analyzed. For each, the previously published, refined unit cell may be rotated clockwise by ~60º for comparison to a layer unit cell. In pyrophyllite, the layer unit cell is ideal and shown to be orthogonal with C2/m symmetry. The agreement between the refined atomic coordinates and those calculated for the layer with C2/m symmetry confirms that the symmetry of the pyrophyllite layer is C2/m. The obliquity of the pyrophyllite refined cell results from the layer stacking and the choice of unit cell, but the interlayer stacking sequence does not disturb the layer symmetry. In contrast, talc has an oblique layer cell, without a mirror plane. For the most part, the distortion of the talc 2:1 layer is probably caused by an elongation of unshared OÀO lateral edges around M1 that creates a slight corrugation of the octahedral sheet surface.