AN OCCURRENCB of DUMORTIERITE NEAR QUARTZSITE, ARIZONA1 Er.Onpn D
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Chemical Composition of Mn-And Cl-Rich Apatites from the Szklary
minerals Article Chemical Composition of Mn- and Cl-Rich Apatites from the Szklary Pegmatite, Central Sudetes, SW Poland: Taxonomic and Genetic Implications Adam Szuszkiewicz 1,* ID , Adam Pieczka 2, Bozena˙ Goł˛ebiowska 2, Magdalena Duma ´nska-Słowik 2 ID , Mariola Marszałek 2 and Eligiusz Szeł˛eg 3 1 Institute of Geological Sciences, University of Wrocław, pl. M. Borna 9, 50-204 Wrocław, Poland 2 Department of Mineralogy, Petrography and Geochemistry, AGH University of Science and Technology Mickiewicza 30, 30-059 Kraków, Poland; [email protected] (A.P.); [email protected] (B.G.); [email protected] (M.D.-S.); [email protected] (M.M.) 3 Department of Geochemistry, Mineralogy and Petrography, Faculty of Earth Sciences, University of Silesia, B˛edzi´nska60, 41-200 Sosnowiec, Poland; [email protected] * Correspondence: [email protected] Received: 6 July 2018; Accepted: 9 August 2018; Published: 14 August 2018 Abstract: Although calcium phosphates of the apatite group (apatites) with elevated contents of Mn are common accessory minerals in geochemically evolved granitic pegmatites, their Mn-dominant M1 M2 X analogues are poorly studied. Pieczkaite, Mn2 Mn3(PO4)3 Cl, is an exceptionally rare Mn analogue of chlorapatite known so far from only two occurrences in the world, i.e., granitic pegmatites at Cross Lake, Manitoba, Canada and Szklary, Sudetes, SW Poland. In this study, we present the data on the compositional variation and microtextural relationships of various apatites highly enriched in Mn and Cl from Szklary, with the main focus on compositions approaching or attaining the stoichiometry of pieczkaite (pieczkaite-like apatites). -
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. -
The Journal of Gemmology Data Depository Photomicrographs To
The Journal of Gemmology Data Depository Photomicrographs to accompany the article: Hänni H.A., Brunk R. and Franz L. 2021. An investigation of grinding hardness of some ornamental stones. Journal of Gemmology, 37(6), 2021, 632–643, https://doi.org/10.15506/JoG.2021.37.6.632. The following photomicrographs of thin sections of the samples were made with a Leica DFC490 camera mounted on a Leica DMRD polarising microscope with transmitted light. For each sample, figure A shows the sample in plane-polarised light (II Pol.) and figure B with crossed polarisers (X Pol.); the sample numbers correspond to those in the article. Photomicrographs © L. Franz. 1 1 Aventurine quartz, green: Foliated matrix with aligned quartz (Qz) grains, fuchsite (Fu) tablets and accessory zircon (Zrn). 2 2 Aventurine quartz, orangey red: Mylonitic fabric with quartz (Qz) ribbons and recrystallized grains as well as intergrowths of muscovite with hematite (Ms & Hem). 3 3 Chalcedony, light grey: Intensely interlocked chalcedony (Chc) crystals with random orientation. 4 4 Chrysoprase: In a matrix of tiny chalcedony (Chc) and quartz (Qz) crystals, larger quartz aggregates occur. In microfractures, palisade-shaped chalcedony crystals and quartz grains formed. 5 5 Dumortierite: A banded texture with layers rich in dumortierite (Dum), dumortierite and quartz (Dum & Qz), quartz (Qz) and tourmaline (Tur). 6 6 Granite: The holocrystalline fabric is made up of subhedral plagioclase (Pl), orthoclase (Or), biotite (Bt) and anhedral quartz (Qz). 7 7 Green quartz: A granoblastic texture made up of large quartz (Qz) crystals as well as a microfolded layer of fuchsite (Fu). 8 8 Heliotrope (bloodstone): Green, brown and colourless accumulations of chalcedony (Chc) are recognizable. -
Fibrous Nanoinclusions in Massive Rose Quartz: the Origin of Rose Coloration
American Mineralogist, Volume 86, pages 466–472, 2001 Fibrous nanoinclusions in massive rose quartz: The origin of rose coloration JULIA S. GOREVA,* CHI MA, AND GEORGE R. ROSSMAN Division of Geological and Planetary Sciences, California Institute of Technology, MS 100-23, Pasadena, California 91125, U.S.A. ABSTRACT Pink nanofi bers were extracted from rose quartz from 29 different pegmatitic and massive vein localities throughout the world. Their width varied from 0.1 to 0.5 µm. On the basis of optical absorp- tion spectra of the fi bers and the initial rose quartz, we conclude that these nanofi brous inclusions are the cause of coloration of massive rose quartz worldwide. These fi bers do not occur in the rare, euhedral variety of pink quartz. Redox and heating experiments showed that the pink color of the fi bers is due to Fe-Ti intervalence charge transfer that produces an optical absorption band at 500 nm. Based on the XRD patterns and characteristics of pleochroism, the best match for these inclusions is dumortierite. However, FTIR and Raman spectra consistently did not exactly match the standard dumortierite patterns, suggesting that this fi brous nano-phase may not be dumortierite itself, but rather a closely related material. INTRODUCTION Other workers have suggested that the color of rose quartz is 2+ 4+ The rose variety of quartz is known and valued from time due to intervalence charge transfer (IVCT) between Fe + Ti 3+ 3+ 4+ immemorial as an item of beauty, a source of rock for decorative → Fe + Ti (Smith et al. 1978) or between substitutional Ti 3+ carvings, and as a jewelry stone. -
Some Uncommon Sapphire “Imitations”: Blue Co-Zirconia, Kyanite & Blue Dumortierite Dr Michael S
Some Uncommon Sapphire “Imitations”: Blue Co-zirconia, Kyanite & Blue Dumortierite Dr Michael S. Krzemnicki Swiss Gemmological Institute SSEF [email protected] 筆者滙報數個瑞士珠寶研究院(SSEF)近期收到 in the ring showed a negative RI reading 要求鑑證的藍色寶石,經檢測後確定其中包括 (above 1.79), an isotropic optical character 一些非常罕見的藍寶石模擬石:含錮氧化鋯、 (polariscope) and thus no pleochroism at all. 藍晶石及藍線石等。 Under the microscope, we saw no inclusions, however a slightly greenish reaction under Sapphires are among the most abundant gems the LWSW and there was a weaker similar we receive at the Swiss Gemmological Institute reaction under SWUV lamps. Based on these (SSEF) for testing. From time to time, however, properties and a chemical analysis by X-ray we are quite surprised by the imitations which fluorescence (EDXRF), the blue stone was we find among the goods sent in and this can readily identified as cubic zirconia (ZrO2). then be disappointing news for the clients. In Having seen this artificial product in a wide the following short note, the author presents a range of colours, the author had not previously few uncommon imitations identified recently at seen one of such a saturated and attractive the SSEF. Identification of these imitations is blue. Based on literature (Nassau 1981) the straightforward and should be no problem for analysed traces of cobalt in that stone have any experienced gemmologist. been identified as the colouring element in this specimen. The absorption spectrum of the stone The first case is that of an attractive blue (Fig. 2) – although superposed by several rare faceted stone of approximately 1.4 ct, set in a ring with diamonds (Fig. -
Significance of Dumortierite in an Aluminosilicate.Rich
t37 CanadianMineralogist Vol. 3 I, pp. 137-146 (1993) SIGNIFICANCEOF DUMORTIERITE IN AN ALUMINOSILICATE.RICHALTERATION ZONE, LOUVICOURT,OUEBEC MEHMETF. TANER BP Resources Canala Limited, lzs Mines Selbaie' Case Postale j70, Joutel, Qulbec JOY IN0 ROBERTF.MARTIN Departmentof Eanhand Planetary Sciences, McGill Universiry' 3450University Street, Montr,1al, Qutbec H3A 2A7 ABSTRACI A dumortierite-bearing,aluminosilicate-rich zone of hydrothermalalteration has been found in the northeasternsector of Louvicourt Township, in-the Abitibi greenstonebelt, Val d'Or area Quebec.The affected schists(metavolcanic rocks of &e Malartic Group) are andalusite-bearing;they are located near the southerncontact of^the Bevcon pluton. The presenceof dumonieritemakes the rocks pinkish. Its a andb cell parameters,I 1.822(5) nd20.251(7) A, arelarger than usually reported, and mayreflect the presence of vlMg andlvAI. Thec diminsionis 4.698(I ) A. Theaverage chemical composition of thedumortierite in two samplesdiffers slightly: (A16.sA4g0.r2Ti0.mFeo.oootro.zs)x.0rB(Si2.8lAl0.r4Po.oa)>z.seorz.0e(oH)q.q.l (surfaceexposure) and (A16.62Mg6'67Ti6.orF"o.orio.r)*.ril$ir-A1o*i,o.oJo-6"-(OH)1.16 (subsurface).The dumortieritereplaces andalusite, whi;ii:fodA diiring iii6 miitari<irphis;';d aafom;ri;nbf the intenselyleached metavolcanic rocks. The introductionof boron thus occunedlate. The presenceof dumortierite,here described for the fint time in theAbitrbi greenstonebelt, provides.avaluable targetfor further explorationbecause of the link betweenperaluminous altered rocks -
Transition from Staurolite to Sillimanite Zone, Rangeley Quadrangle, Maine
CHARLES V. GUIDOTTI Department of Geology and Geophysics, University of Wisconsin, Madison, Wisconsin 53706 Transition from Staurolite to Sillimanite Zone, Rangeley Quadrangle, Maine ABSTRACT GENERAL GEOLOGICAL SETTING Ordovician and Silurian to Devonian pelitic schist, conglomerate, quartzite, calc-silicate Study of pelitic schists in the Rangeley Figure 1 shows the location of the area granulite, and biotite schist. Post-tectonic, area, Maine, by means of petrographic, and a generalized geologic map of the shallow-dipping, adamellite sheets intrude x-ray, and electron-microprobe techniques southwestern third of the Rangeley quad- the metamorphosed strata. As illustrated in enables definition of the isogradic reaction rangle based upon Moench (1966, 1969, Figure 1, the isograds have a clear spacial relating the staurolite and lower sillimanite 1970a, 1970b, 1971). The rocks in this area relation to the distribution of the adamel- zones. The reaction is a discontinuous one consist of tightly folded, northeast-trending lites; but in a few cases, the adamellite and can be shown on an AFM projection as the tie line change from staurolite + chlorite to sillimanite 4- biotite. This topology change, in conjunction with the min- eralogical data provides the equation: Staur + Mg-Chte + Na-Musc + (Gam?) Sill + Bio + K-richer Muse + Ab + Qtz + H20. This reaction should result in a sharp isograd in the field but in fact is found to be spread out over a zone which is called the transition zone. It is proposed that this zene results from buffering of fH20 by means of the equation above. Buffering of fH.,o by continuous reactions also appears to be taking place in the lower sillimanite zone. -
The Seven Crystal Systems
Learning Series: Basic Rockhound Knowledge The Seven Crystal Systems The seven crystal systems are a method of classifying crystals according to their atomic lattice or structure. The atomic lattice is a three dimensional network of atoms that are arranged in a symmetrical pattern. The shape of the lattice determines not only which crystal system the stone belongs to, but all of its physical properties and appearance. In some crystal healing practices the axial symmetry of a crystal is believed to directly influence its metaphysical properties. For example crystals in the Cubic System are believed to be grounding, because the cube is a symbol of the element Earth. There are seven crystal systems or groups, each of which has a distinct atomic lattice. Here we have outlined the basic atomic structure of the seven systems, along with some common examples of each system. Cubic System Also known as the isometric system. All three axes are of equal length and intersect at right angles. Based on a square inner structure. Crystal shapes include: Cube (diamond, fluorite, pyrite) Octahedron (diamond, fluorite, magnetite) Rhombic dodecahedron (garnet, lapis lazuli rarely crystallises) Icosi-tetrahedron (pyrite, sphalerite) Hexacisochedron (pyrite) Common Cubic Crystals: Diamond Fluorite Garnet Spinel Gold Pyrite Silver Tetragonal System Two axes are of equal length and are in the same plane, the main axis is either longer or shorter, and all three intersect at right angles. Based on a rectangular inner structure. Crystal shapes include: Four-sided prisms and pyramids Trapezohedrons Eight-sided and double pyramids Icosi-tetrahedron (pyrite, sphalerite) Hexacisochedron (pyrite) Common Tetragonal Crystals: Anatase Apophyllite Chalcopyrite Rutile Scapolite Scheelite Wulfenite Zircon Hexagonal System Three out of the four axes are in one plane, of the same length, and intersect each other at angles of 60 degrees. -
Geologic Map of the Southern Ivrea-Verbano Zone, Northwestern Italy
•usGsscience for a changing world Geologic Map of the Southern Ivrea-Verbano Zone, Northwestern Italy By James E. Quick,1 Silvano Sinigoi,2 Arthur W. Snoke,3 Thomas J. Kalakay,3 Adriano Mayer,2 and Gabriella Peressini2·4 Pamphlet to accompany Geologic Investigations Series Map I- 2776 1U. S. Geological Survey, Reston, VA 20192- 0002. 2Uni versita di Trieste, via Weiss 8, 341 27 Trieste, ltalia. 3Uni versity of Wyoming, Larami e, WY 8207 1- 3006. 4Max-Planck-lnstitut ft.ir Chemi e, J.J. Becherweg 27, 55 128 Mainz, Germany. 2003 U.S. Department of the Interi or U.S. Geological Survey COVER: View of the Ponte della Gula, an ancient bridge spanning the Torrente Mastellone approximately 2 kilometers north of the village of Varallo. Diorite of Valsesia crops out beneath the bridge. Photograph by ADstudia, Silvana Ferraris, photographer, Pizza Calderini, 3-13019 Varallo Sesia ([email protected]) INTRODUCTION REGIONAL SETTING The intrusion of mantle-derived magma into the deep conti The Ivrea-Verbano Zone (fig. 1) is a tectonically bounded sliver nental crust, a process commonly referred to as magmatic of plutonic and high-temperature, high-pressure metamorphic underplating, is thought to be important in shaping crustal com rocks in the southern Alps of northwestern Italy (Mehnert, position and structure. However, most evidence for this process 1975; Fountain, 1976). To the northwest, it is faulted against is indirect. High P-wave velocities and seismic-reflection profiles the basement of the Austro-Alpine Domain by the lnsubric Line, reveal that much of the deep continental crust is dense and a major suture zone that separates the European and Apulian strongly layered, consistent with the presence of layered mafic plates (Schmid and others, 1987; Nicolas and others, 1990). -
Control of Material Transport and Reaction Mechanisms by Metastable Mineral Assemblages: an Example Involving Kyanite, Sillimanite, Muscovite and Quartz
Fluid-Mineral Interactions: A Tribute to H. P. Eugster © The Geochemical Society, Special Publication No.2, 1990 Editors: R. J. Spencer and I-Ming Chou Control of material transport and reaction mechanisms by metastable mineral assemblages: An example involving kyanite, sillimanite, muscovite and quartz C. T. FOSTER,JR. Geology Department, University ofIowa, Iowa City, Iowa 52242, U.S.A. Abstract-Metastable mineral assemblages strongly influence reaction mechanisms and material transport when a new mineral grows in a metamorphic rock. The effects exerted by the metastable assemblages on the reactions that take place when sillimanite grows in a kyanite-bearing rock are examined using metastable elements of activity diagrams and irreversible thermodynamic principles. The results show that a commonly inferred reaction mechanism, where muscovite assists in the growth of sillimanite at the expense of kyanite, is a consequence of material transport constraints imposed by a metastable mineral assemblage in the matrix that separates growing sillimanite from dissolving kyanite. INTRODucnON pressures and temperatures represented by points I, II, and III (Fig. la) is shown in Fig. lb. ONEOFTHEPRIMARYcontrols on mineral textures Sillimanite nuclei first form in sites in the rock that develop during metamorphism is the distri- with the lowest activation energy for nucleation of bution of minerals in a rock at the time when a sillimanite. Under many metamorphic conditions, new mineral nucleates. The distribution of the new the low energy sites for sillimanite nucleation in mineral is strongly influenced by the abundance pelites appear to be in micas, because this is where and location of other minerals with favorable nu- sillimanite is commonly first observed with in- cleation sites for it. -
Glossary of Gemstone and Crystal Correspondences
GLOSSARY OF PRIMARY GEMSTONES USED IN METAPHYSICAL ENERGY WORK benebell wen Table of Contents Basics of Stone and Crystal Work .................. 2 R ........................................................................... 32 Clearing the Stone’s Qi ........................................ 2 S ............................................................................ 33 When Not to Clear a Stone’s Qi ...................... 4 T ........................................................................... 36 Glossary of Gemstones & Crystals ................. 6 U ........................................................................... 38 A .............................................................................. 6 V ........................................................................... 38 B ............................................................................ 10 W ......................................................................... 39 C ........................................................................... 12 X ........................................................................... 39 D ........................................................................... 14 Y............................................................................ 39 E ............................................................................ 15 Z ........................................................................... 40 F ............................................................................ 16 General Correspondences -
Holtite and Dumortierite from the Szklary Pegmatite, Lower Silesia, Poland A
The University of Maine DigitalCommons@UMaine Earth Science Faculty Scholarship Earth Sciences 4-1-2011 Holtite and Dumortierite from the Szklary Pegmatite, Lower Silesia, Poland A. Pieczka Edward S. Grew University of Maine - Main, [email protected] L. A. Groat R. J. Evans Follow this and additional works at: https://digitalcommons.library.umaine.edu/ers_facpub Part of the Earth Sciences Commons Repository Citation Pieczka, A.; Grew, Edward S.; Groat, L. A.; and Evans, R. J., "Holtite and Dumortierite from the Szklary Pegmatite, Lower Silesia, Poland" (2011). Earth Science Faculty Scholarship. 42. https://digitalcommons.library.umaine.edu/ers_facpub/42 This Article is brought to you for free and open access by DigitalCommons@UMaine. It has been accepted for inclusion in Earth Science Faculty Scholarship by an authorized administrator of DigitalCommons@UMaine. For more information, please contact [email protected]. Mineralogical Magazine, April 2011, Vol. 75(2), pp. 303–315 Holtite and dumortierite from the Szklary Pegmatite, Lower Silesia, Poland 1 2 3 3 A. PIECZKA ,E.S.GREW ,L.A.GROAT AND R. J. EVANS 1 Department ofMineralogy, Petrography and Geochemistry, AGH À University ofScience and Technology, Mickiewicza 30, 30-059 Krako´w, Poland 2 Department ofEarth Sciences, University ofMaine, 5790 Bryand Global Sciences Center, Orono, Maine 04469- 5790, USA 3 Department ofEarth and Ocean Sciences, University ofBritish Columbia 6339 Stores Road, Vancouver, British Columbia V6T IZ4, Canada [Received 24 November 2010; Accepted 30 March 2011] ABSTRACT The Szklary holtite is represented by three compositional varieties: (1) Ta-bearing (up to 14.66 wt.% Ta2O5), which forms homogeneous crystals and cores within zoned crystals; (2) Ti-bearing (up to 3.82 wt.% TiO2), found as small domains within the core; and (3) Nb-bearing (up to 5.30 wt.% Nb2O5,) forming the rims of zoned crystals.