Sadanagaite and Magnesio.Sadanagaite, New Silica-Poor Members of Calcic Amphibole from Japan

Total Page:16

File Type:pdf, Size:1020Kb

Sadanagaite and Magnesio.Sadanagaite, New Silica-Poor Members of Calcic Amphibole from Japan American Mineralogist, Volume 69, pages 465471, 19E4 Sadanagaiteand magnesio.sadanagaite,new silica-poor membersof calcic amphibole from Japan Hrppnxo Sntrraezerr Geological Institute, Faculty of Science University of Tolcyo, Hongo, Tolcyo l13, Japan Mrcnrerr Buuxor Department of Mineralogy, The University Museum University of Tolcyo, Hongo, Tolcyo 113, Japan nxo Tonnu Ozewe Mineralogical Institute, Faculty of Science University of Tolcyo, Hongo, Tolcyo ll3, Japan Abstract Sadanagaite,(K,Na)CazGe2*,Mg,Al,Fe3*,Ti)r[(Si,AlhO22(OH)2] where Fe2* = Mg, Al = Fe3* and Si < 5.5, and its Mg-rich analogue,magnesio-sadanagaite Fe2+ < Mg, are extremely SiO2-poor new amphiboles, which require the compositional extension of the edenite-pargasiteseries, and amending of the classification and nomenclature of amphi- boles (Leake, 1978). Theseare monoclinic,C2, Cm or Cllm; a = 9.922(10),b : 1E.03(2),c : 5.352(9)4,B: 105.30(10f,Z = 2 for sadanagaitewith Si - 5.0, and a : 9.964(2),D : 18.008(3),c : 5.354(2)4,B = 105.55(2)",2= 2 for magnesio-sadanagaitewith Si:5.0. The strongest lines in the X-ray powder pattern for magnesio-sadanagaiteare: 8.48(80)(ll0), 3.39(40Xl3l), 3.28(100X240),3.15(70)(3r0), 2.951(50X22r),2.823(30)(330), 2.766(45)(33r), 2.707(60Xl5l),2.594(35X061),2.162(55)(261),1.654(30X461), thesebeing similar to thoseof X-ray powder patterns of SiO2-poorcalcic amphiboles, especially kaersutite. Both specieshave very similar physical properties, and are dark brown to black with a vitreousluster. Streak very light brown. Cleavage{110}, perfect. H (Mohs) : 6. Density (calc.) 3.30 g/cm3 for sadanagaite and 3.27 g/cm3 for magnesio-sadanagaite.Optically biaxial positive with2V = 80-X)" (meas.), 86" (calc.) for sadanagaite,and with2V close to 90o(meas,), 88'(calc.) for magnesio-sadanagaite.Refractive indices: a = 1.673(2),F = 1.684(2),y-1.697(2);c:Z=28'(sadanagaite),anda=1.674(2),8--1.686(2),y= 1.699(2);c:Z : 26" (magnesio-sadanagaite).Pleochroism strong with X' = pale brown to Z' - greenish brown (sadanagaite)and with X' = colorless to Z' = brownish yellow (magnesio-sadanagaite). The minerals are found in two separate localities, Yuge and Myojin Islands, Japan, where they occur in Al-, Ti- and Fe-rich skarns in recrystallized limestone beds, forming bands with vesuvianite, spinel-hercynite, sphene, ilmenite and apatite in the former locality, and forming small lenses with titaniferous fassaite, vesuvianite, spinel-hercynite, sphene,ilmenite, magnetite,apatite and perovskite in the latter. Among them the peculiar composition of titaniferous fassaite is discussed with special reference to its extremely SiO2-poor, Al2O3- and TiO2-rich composition. The names are for Professor Ryoichi Sadanaga,Mineralogical Institute, University of Tokyo, in recognition of his outstanding contributions to the fields of mineralogy and crystallography. I Presentaddress: Geological Department, Geological Survey ofJapan, Higashi l-l-3, Yatabe, Ibaraki 305, Japan. 0003-004)uE4l0506-965$02. 00 466 SHIMAZAKI ET AL,: SADANAGAITE AND MAGNESIO-SADANAGAITE Introduction brown seams intercalated with limestone in the quarry. The classification and nomenclature of amphiboles by Myojin Island, one of islands known as the Shisaka Leake (1978)defines no lower limit of Si content in calcic Islands, consists largely of somewhat gneissosegranitic amphiboles,although a prefix "subsilicic" is recom- rocks and gneisswith some limestonebeds. Sato (1926) mendedwhen the number of Si is less than 5.75 on the first reported the occurrenceofclinopyroxene from skarn basis of 23 oxygens. The occurrence of amphibole with lenses in one limestone bed, and subsequently Kuno Si : 5.27has beenreported by Appleyard (1975)and the (1960) described this as titaniferous pyroxene, and necessity of new end member NaCa2Mg3Al2Si5Al3 Miyahisa et al. (1980)as fassaite.The dark colored lenses O22(OH)2("Al-pargasite") has been suggested(Bunch in the limestone bed include locally amphibolesof parga- and Okrusch, 1973;Doolan, Zen and Bence, 1978). site to magnesio-sadanagaitecomposition in addition to This contribution provides natural examplesof amphi- the above clinopyroxene. boles with lower Si than the above composition from two separate localities, Yuge and Myojin Islands, Ehime Occurrence and associated minerals Prefecture, Japan. The composition of these amphiboles According to the geological map compiled for Ehime is so different from that of pargasite with regard to the Prefecture (1962),Yuge and Myojin Islands are situated number of Si that they are proposed as new Si-poor near the boundary between the Paleozoic-MesozoicChi- members(Si < 5.5) of the pargasite series. The minerals chibu Belt and the Ryoke Metamorphic Bett (Fig. l). and mineral names, sadanagaiteand magnesio-sadana- Yuge Island belongs to the former belt with the intrusion gaite, have been approvedby the Commissionon New of the Mesozoic Hiroshima-type granitic rocks. Myojin Minerals and Mineral Names, IMA (CommissionNos. Island belongsto the latter belt, and weakly gneissose 80-27and 82-102).The names are for Emeritus Professor granitic rocks are associatedwith high temperature-low Ryoichi Sadanaga,Mineralogical Institute, University of pressure-type metamorphic rocks. Both localities are Tokyo, in recognition of his outstanding contributions to only about 15 km from each other, and are thought to the field of mineralogy and crystallography. Type speci- have similar geologic environments, although they are mens have been deposited in the Department of Mineral- located in diferent geologic belts. No tectonic zone ogy, the University Museum, University of Tokyo, Ja- separatesthem, and the boundary between the belts is pan. basedonly on the metamorphic grade. Both Yuge and Myojin are small islands located in the In the Yuge limestone quarry, sadanagaite-bearing Seto Inland Sea, southwesternJapan (Fig. l). In Yuge skarn occurs as seamsin limestone with variable widths Island, where a limestonequarry has been operated,a up to a maximum of 50 cm. The skarn seamsusually have sadanagaite-bearingvesuvianite skarn occurs as dark a symmetrical structure, that is, they consist of a wollas- rrd t3s. o'+ + HONSHU ..i.,,,$ -------sS "t4 ll$'r'-- -t,' 5 '--.^*g gES O SOKM 0t€rss0€E OR ilIIE Fig. l. Location and simplified geology of the Yuge and Myojin Islands, Ehime Prefecture, Japan. SHIMAZAKI ET AL.: SADANAGAITE AND MAGNESIO-SADANAGAITE 467 tonite zone, a garnet-vesuvianite zone, and a vesuvian- ent of the skarn, in contrast with the Yuge occurrence. ite-sadanagaite zone, traversing from limestone to the The skarn includes, besides clinopyroxene, various center of the seam. Sadanagaitemay be lacking in the amounts of spinel, vesuvianite, magnesio-sadanagaiteto central vesuvianitezone of some seams.The sadanagaite- pargasite, phlogopite and minor amounts of sphene, il- bearing zone occurs as a compact, dark brown band, menite, magnetite, pyrrhotite, apatite and perovskite. consisting of vesuvianite and sadanagaitewith minor Both clinopyroxene and magnesio-sadanagaitefrom this amounts of spinel, sphene, ilmenite and apatite. Sadana- locality are short-prismatic to granular in shape with a gaite appears as isolated prismatic crystals with a maxi- maximum diameter of a few hundred microns. mum length of I mm or as polycrystalline aggregatesin The composition of the clinopyroxene has been debat- matrix vesuvianite. The composition of sadanagaitesis ed since the first description by Sato (1926).Kuno (1960) quite variable with respect to SiO2as will be describedin showed that the clinopyroxene is rich in AlzOr (6.89 the following section and shown in Table l. wt.Vo) and TiOz Q.47%) by wet chemical analysis. Preliminary electron microprobe analyses show that Miyahisa et al. (1980)concluded that it is fassaitewith up the vesuvianite is rich in titanium with TiO2 contents of 5 to 5 wt.%oAl2O3 using the electron probe microanalyzer. wt.Vo or more. The spinel is hercynite with variable Most of the skarn lenses contain clinopyroxenes with amountsof the spinel molecule. Amounts of up to 5 wt.Vo compositions similar to those given by Kuno (1960)and Al2O3 are present in the sphene. Ilmenite has a small Miyahisa et al. (1980). The associated amphiboles are amount of the geikielite molecule. (ferroan) pargasite to less commonly magnesio-hasting- In Myojin Island, the magnesio-sadanagaite-bearing site. skarn occurs as a lens or as an irregularly shapednodule The bulk chemical compositions of the lensesare quite in crystalline limestone. Some lenses show a structure variable, and in some rare lensesthe compositionsof the similar to that of boudinage.The size of the lens or nodule clinopyroxene and amphibole become very Si-poor, and although variable rangesup to several tens of centimeters Al- and Ti-rich. Magnesio-sadanagaitegiven in Table l, in width. The occurrenceofthe skarn is reported in detail No. 4, is an example from an extremely Si-poor lens. The as a fassaite-spinelrock by Miyahisa et al. (19E0). As associatedclinopyroxene is also unusually Si-poor, with noted in their paper, clinopyroxene is the main constitu- the number of Si : 1.3 on the basis of 6 oxvsens. An Table l. Electron microprobe analysesof sadanagaitesfrom the Yuge (Y) and Myojin (M) skarns No. r (Y) 4 0,r) s (Y) sio2 30.2 29.9 3I. I 32.L 33.5 29.5 Tio2 4.0 4.3 4.5 3.2 2.L 4.0 A1203 24.8 22.6 22.5 22.0 L9.7 23.2 FeOr L5.2 L7.4 L6.2 L3.7 17.8 15.4 MnO 0.1 0.3 0.4 0.1 0.5 0.3 Mgo 6.6 6.1 6-6 8.0 6.4 CaO L2.3 1r.9 L2,0 L2.5 11.9 1r. 9 Na2O r. u 0,6 0.6 o.7 L.2 K2o 3.7 3.7 3.6 3.8 3.r 3.5 Total 97.9 95.8 t I .5 96.1 96.2 97.2 Nrmbers of cations on the basis of 23 oxygens si 4.6il n.eo) q.ttl 4.e5) s.zl'l l.szl lrrV ,.rrj8'00 ..rnJt'oo ,.rrJt.oo ,.orjt.oo z.tale-oo 3.4sJ8-oo -, vr Ti -J+ !e Fe2+ Mn M9 Ca 2.01 2.0r 1.99 r.99 I.97 L-97 2.07 2.07 2.00 2.00 1.96 1.96 Na 0.2e1_ -_ o.r7l o.tel o.zzl o.gzl o.2o'l K o.t.Jt'oo o.toJo'tt o.rrJo'tt o.rulo't' o.rrJo''e o..rlo'tt *Total iron.
Recommended publications
  • Optical Properties of Common Rock-Forming Minerals
    AppendixA __________ Optical Properties of Common Rock-Forming Minerals 325 Optical Properties of Common Rock-Forming Minerals J. B. Lyons, S. A. Morse, and R. E. Stoiber Distinguishing Characteristics Chemical XI. System and Indices Birefringence "Characteristically parallel, but Mineral Composition Best Cleavage Sign,2V and Relief and Color see Fig. 13-3. A. High Positive Relief Zircon ZrSiO. Tet. (+) 111=1.940 High biref. Small euhedral grains show (.055) parallel" extinction; may cause pleochroic haloes if enclosed in other minerals Sphene CaTiSiOs Mon. (110) (+) 30-50 13=1.895 High biref. Wedge-shaped grains; may (Titanite) to 1.935 (0.108-.135) show (110) cleavage or (100) Often or (221) parting; ZI\c=51 0; brownish in very high relief; r>v extreme. color CtJI\) 0) Gamet AsB2(SiO.la where Iso. High Grandite often Very pale pink commonest A = R2+ and B = RS + 1.7-1.9 weakly color; inclusions common. birefracting. Indices vary widely with composition. Crystals often euhedraL Uvarovite green, very rare. Staurolite H2FeAI.Si2O'2 Orth. (010) (+) 2V = 87 13=1.750 Low biref. Pleochroic colorless to golden (approximately) (.012) yellow; one good cleavage; twins cruciform or oblique; metamorphic. Olivine Series Mg2SiO. Orth. (+) 2V=85 13=1.651 High biref. Colorless (Fo) to yellow or pale to to (.035) brown (Fa); high relief. Fe2SiO. Orth. (-) 2V=47 13=1.865 High biref. Shagreen (mottled) surface; (.051) often cracked and altered to %II - serpentine. Poor (010) and (100) cleavages. Extinction par- ~ ~ alleL" l~4~ Tourmaline Na(Mg,Fe,Mn,Li,Alk Hex. (-) 111=1.636 Mod. biref.
    [Show full text]
  • MINERALOGY for PETROLOGISTS Comprising a Guidebook and a Full Color CD-ROM, This Reference Set Offers Illustrated Essentials to Study Mineralogy, Applied to Petrology
    MINERALOGY for PETROLOGISTS for MINERALOGY Comprising a guidebook and a full color CD-ROM, this reference set offers illustrated essentials to study mineralogy, applied to petrology. While there are some excellent reference works available on this subject, this work is unique for its data richness and its visual character. MINERALOGY for PETROLOGISTS With a collection of images that excels both in detail and aesthetics, 151 minerals are presented in more than 400 plates. Different facies and paragenesis, both in natural polarized light, are shown for every mineral and optical data, sketches of the crystal habitus, chemical composition, occurrence and a brief description are Optics, Chemistry and Occurrences included. The accompanying user guide gives a general introduction to microscope mineral observation, systematic mineralogy, mineral chemistry, occurrence, of Rock-Forming Minerals stability, paragenesis, structural formula calculation and its use in petrology. This compact set will serve as a field manual to students, researchers and Michel Demange professionals in geology, geological, mining, and mineral resources engineering to observe and determine minerals in their studies or field work. Dr. Michel Demange has devoted his career to regional geology and tectonics of metamorphic and magmatic terranes and to ore deposits. Graduated from the École Nationale Supérieure des Mines de Paris and holding a Docteur-es-Sciences from the University Pierre et Marie Curie, Paris VI, he has been active in a rich variety of geological projects and investigations around the world. In combination with his teaching and research activities at the École des Mines in Paris, France, he headed various research studies. This book benefits from the great experience in field M.
    [Show full text]
  • Spring 2002 Gems & Gemology
    Spring 2002 VOLUME 38, NO. 1 EDITORIAL 1 Richard T. Liddicoat: Celebrating 50 Years of Leadership William E. Boyajian FEATURE ARTICLES 2 The Ultimate Gemologist: A Tribute to Richard T. Liddicoat Dona M. Dirlam, James E. Shigley, and Stuart D. Overlin A look at the extraordinary career of Richard Liddicoat. 14 Portable Instruments and Tips on Practical Gemology in the Field Edward W. Boehm An essential guide to the use of portable instruments when purchasing gems. 28 Liddicoatite Tourmaline from Anjanabonoina, Madagascar Dona M. Dirlam, Brendan M. Laurs, Federico Pezzotta, and William B. (Skip) Simmons pg. 3 Explores the world’s primary source of this remarkable calcium-rich lithium tourmaline, named in honor of Richard T. Liddicoat. 54 Star of the South: A Historic 128 ct Diamond Christopher P. Smith and George Bosshart A history and characterization of this famous diamond. NOTES AND NEW TECHNIQUES 66 Identification of Yellow Cultured Pearls from the Black-Lipped Oyster Pinctada Margaritifera Shane Elen How absorption features can establish the origin of these cultured pearls. pg. 22 73 Serendibite from Sri Lanka Karl Schmetzer, George Bosshart, Heinz-Jürgen Bernhardt, Edward J. Gübelin, and Christopher P. Smith A characterization of this rare gem material from Sri Lanka. REGULAR FEATURES 80 Gem Trade Lab Notes • Color grade vs. value for fancy-color diamonds • Diamond with eclogitic inclusions • Diamond with a large void • Genthelvite: A second occurrence • Jadeite carving: Assembled, dyed, and impregnated • Coated natural pearls •
    [Show full text]
  • Pargasites in Lherzolite and Websterite Inclusions from Itinome-Gata, Japan
    J. Japan. Assoc. Min. Petr. Econ. Geol. 68, 303-310, 1973 PARGASITES IN LHERZOLITE AND WEBSTERITE INCLUSIONS FROM ITINOME-GATA, JAPAN KEN-ICHIRO AOKI and IKUKO SHIBA Institute of Mineralogy, Petrology and Economic Geology, Tohoku University, Sendai, Japan Pargasite occupies up to 4 volume per cent of lherzolite inclusions and up to 8 per cent of websterite inclusions. It occurs as discrete primary crystals and as interstitial grains among other minerals averaging less than 2 volume per cent. New analyses are presented for six representative pargasites. They are characterized by high Cr2O2 and wide variation of K2O and Mg/(Mg+Fe) ratio. The following origin of the pargasites is hypothsized from the mineralogy and chemist ry of the host rocks. Original garnet lherzolite and websterite were located at a depth of up to 50 to 75km. During upward transport, to 25km deep in the uppermost part of the mantle, the garnet was finally transformed to olivine+plagioclase+spinel and both orthopyroxene and clinopyroxene were recrystallized toward a relatively rich Tschermak's molecule. Jadeite and Tschermak's components separated from pyroxenes and silica liberated from the breakdown of garnet produced plagioclase, pargasite and orthopyroxene. However, minor newly-formed minerals were not always in equilibrium with major consti tuents. It is demonstrated that the lherzolite mantle just below the M-discontinuity contains only up to 0.04 per cent water. INTRODUCTION (Kushiro, 1970). Because the former has been found only in kimberlite diatremes at Oxburgh (1964) suggested that am Buell Park, Arizona (Aoki, et al., 1972), it phibole would be stable in an upper mantle of peridotite composition, playing a very is thought to be a rare occurrence in the important role in basaltic magma genera mantle.
    [Show full text]
  • Cl-Rich Amphiboles As Record for Hydrothermal Processes at Very
    Cl-rich amphiboles as record for hydrothermal processes at very high temperatures in the deep oceanic crust: brine/rock interaction experiments and investigation on natural rocks Von der Naturwissenschaftlichen Fakultät der Gottfried Wilhelm Leibniz Universität Hannover zur Erlangung des Grades Doktorin der Naturwissenschaften (Dr. rer. nat.) genehmigte Dissertation von Adriana Miriam Currin Sala, M. Sc (Niederlande) 2018 Referent: Prof. Dr. rer. nat. Jürgen Koepke Korreferenten: Prof. Dr. rer. nat. Wolfgang Bach Prof. Dr. sci. nat. Ulrich Heimhofer Tag der Promotion: 15.11.2018 2 Abstract Interactions between rock and high temperature seawater-derived fluids are recorded in hydrothermal veins and dykelets that cross-cut layered olivine gabbros deep in the plutonic section of the Samail Ophiolite, Wadi Wariyah, Sultanate of Oman. Here we present a study – using petrographic, microanalytical, isotopic, and structural methods – of amphiboles found in the aforementioned veins and dykelets, which show a conspicuous compositional variation from high-Ti magnesiohastingsite and pargasite via magnesiohornblende and edenite, to Cl-rich ferropargasite and hastingsite (with up to 5.4 wt% Cl) and actinolite. These minerals record a wide range of formation conditions from magmatic to hydrothermal at varying water/rock ratios and salinities, while the formation of super Cl-rich amphibole suggests the occurrence of phase separation, and 87Sr/86Sr and stable δ18O isotope analyses confirm the influence of a hydrothermal fluid in a rock-dominated environment. A parallel experimental study was conducted at hydrothermal (500 – 750 °C) and magmatic (900 °C) conditions at pressures of 2 kbar, and fO2 close to NNO, with an amphibole-containing natural olivine gabbro and saline fluid (6, 20 and 50 wt% NaCl).
    [Show full text]
  • CHAPTER 4 - MINERAL CHEMISTRY and METAMORPHIC CONDITIONS A
    - 217 - CHAPTER 4 - MINERAL CHEMISTRY AND METAMORPHIC CONDITIONS a - 218 - Mineral chemistry and metamorphic conditions The aims of this chapter are to present mineral chemical data, to describe the mineral chemistry in relation to parageneses in selected lithologies (with particular reference to high-pressure metamorphic types) and to evaluate the metamorphic conditions under which these parageneses formed in the light of published experimentally and theoretically derived phase equilibria. Finally, a synthesis of pressure-temperature-time (P-T-t) relationships will be presented. Analytical methods and mineral recalculation schemes are described in Appendices 1 and 2. Results of geothermometry calculations are sumarised in Tbj 4.20. SECTION 4.01 The Eclogites 4.01.1 Summary of petrography Detailed petrographic descriptions appear in Chapter 2, the salient features of which are summarised here. The most common parageneses in the eclogites are:- garnet + omphacite +1- amphibole +1- rutile garnet + omphacite + phengite +1- quartz +1- rutile garnet + omphacite + phengite + zoisite +/_ quartz +/_ rut i e. S - 219 - garnet + omphacite + phengite + zoisite + kyanite +1- quartz ^1- rutile Segregations of zoisite + kyanite + quartz occur in some more aluminous types. Occasionally, Na-poor rocks have pale green or blue-green amphibole in textural equilibrium with omphacite and garnet (figure 2.18) which may become an essential or dominant phase, to give:- garnet + amphibole + clinopyroxene +/_ rutile. The phases listed above will be referred to as 'matrix' phases. Solid inclusions are common in the matrix phases (figures 2.19, 2.45). They are not associated with fractures in the garnets and commonly occur in samples where no alteration of garnet rims or matrix grains has occurred.
    [Show full text]
  • Spinel from Mogok, Myanmar—A Detailed Inclusion Study by Raman
    FEATURE ARTICLE Spinel from Mogok, Myanmar—A Detailed Inclusion Study by Raman Microspectroscopy and Scanning Electron Microscopy Myint Myat Phyo, Eva Bieler, Leander Franz, Walter Balmer and Michael S. Krzemnicki ABSTRACT: Mineral inclusions within 100 gem-quality spinels from both primary marble and secondary alluvial mining sites within Myanmar's Mogok Valley were analysed using Raman microspectroscopy and scanning electron microscopy (including backscattered-electron imaging and energy-dispersive spectroscopy). The samples ranged from pink to red, orangey pink to orangey red, and grey to purplish grey. We identified a number of inclusions that are reported here for the first time in Mogok spinel: amphibole (presumably pargasite), anatase, baddeleyite, boehmite, brucite, chlorite, clinohumite, clinopyroxene, diaspore, geikielite, goethite, halite, marcasite, molybdenite, periclase and pyrrhotite. We also found several minerals that were previously known as inclusions in Mogok spinel, including anhydrite, apatite, carbonates (calcite, dolomite and magnesite), chondrodite, elemental sulphur, graphite, iron oxides or iron hydroxides, phlogopite and zircon. We further differentiated the occurrence of inclusions in spinel from different mining sites in Mogok to assess whether these mineral assemblages can enhance our understanding of the geological origin of these gems and whether the inclusions can help separate Mogok spinels from those of other marble-related deposits worldwide. The Journal of Gemmology, 36(5), 2019, pp. 418–435, http://doi.org/10.15506/JoG.2019.36.5.418 © 2019 Gem-A (The Gemmological Association of Great Britain) ince ancient times, gem-quality spinel (ideally imperial jewels, two of which were later integrated into MgAl2O4) has been appreciated for its range British royal jewels (the Black Prince’s ‘Ruby’ and the of colour and often exceptional clarity, and Timur ‘Ruby’; see also Pardieu & Hughes 2008; Yavorskyy today spinel is the second most important and & Hughes 2010; Truong 2017).
    [Show full text]
  • Chromio-Pargasite Naca2mg4crsi6al2o22(OH)2
    Chromio-pargasite NaCa2Mg4CrSi6Al2O22(OH)2 Crystal Data: Monoclinic. Point Group: 2/m. As prismatic crystals, to 1.5 cm, elongated on [001]. Physical Properties: Cleavage: Perfect on {110}. Fracture: Uneven. Tenacity: Brittle. Hardness = 6 D(meas.) = 3.08 D(calc.) = 3.121 Optical Properties: Transparent. Color: Emerald-green to pale green. Streak: Pale green. Luster: Vitreous. Pleochroism: Yellowish to bluish green. Optical Class: Biaxial (+). α = 1.644(2) β = 1.647(2) γ = 1.659(2) 2V(calc.) = 53° Cell Data: Space Group: C2/m. a = 9.9176(1) b = 18.0057(2) c = 5.2865(1) β = 105.395(1)° Z = 2 X-ray Powder Pattern: Akaishi mine, Higashi-Akaishi Mountain, Ehime Prefecture, Japan. 2.546 (100), 2.697 (81), 3.370 (58), 1.514 (55), 2.585 (50), 2.932 (43), 2.346 (42) Chemistry: (1) (2) SiO2 42.90 41.88 TiO2 0.25 Al2O3 12.10 11.84 Cr2O3 5.46 8.83 FeO 1.20 MgO 19.28 18.73 CaO 12.31 13.03 Na2O 3.26 3.60 K2O 0.37 H2O [2.09] 2.09 Total 99.22 100.00 (1) Akaishi mine, Ehime Prefecture, Japan; average of 30 electron microprobe analyses, Fe2+/Fe3+ estimated using the average ferric iron method, H2O from stoichiometry; corresponding to 3+ 2+ (Na0.88K0.07)Σ=0.95(Ca1.89Na0.02Mg0.09)Σ=2.00Mg4.03(Cr0.62Al0.19Fe 0.07Fe 0.07Ti0.03)Σ=0.98(Si6.14Al1.86)Σ=8.00 O22(OH)2. (2) NaCa2Mg4CrSi6Al2O22(OH)2. Polymorphism & Series: Forms a series with pargasite.
    [Show full text]
  • Jog 35 5.Pdf
    GemmologyThe Journal of Volume 35 / No. 5 / 2017 The Gemmological Association of Great Britain Contents GemmologyThe Journal of Volume 35 / No. 5 / 2017 COLUMNS p.386 373 What’s New Multi-colour-temperature lamp|PL-Inspector|AGTA report on Myanmar|ASEAN Gem & p. 388 Jewelry Review|Atypical pearl culturing in P. maxima|Conflict diamonds and Cameroon| Diamond origin identification using fluorescence|Global Diamond Industry 2016|ICGL Klaus Schollenbruch photo Newsletter|Japanese journal online|Raman spectrometer sensitivity|Gold demand trends 2016|Agate Expo DVDs|AGTA ARTICLES 2017 Tucson seminars|Color- Jeff Scovil photo Codex colour referencing system| Feature Articles GemeSquare and MyGem- ewizard apps|Gemewizard 404 Synthetic Emeralds Grown by W. Zerfass: Historical monitor calibration kit|Fabergé Account, Growth Technology, and Properties online|Reopening of The Lap- By Karl Schmetzer, H. Albert Gilg and Elisabeth Vaupel worth Museum of Geology 378 Practical Gemmology 416 Rethinking Lab Reports for the Geographical Moonstone mystery Origin of Gems By Jack M. Ogden 380 Gem Notes Red beryl matrix cabochons| Gemmological Briefs Ceruleite from Chile|Yellow danburite from Namalulu, 424 Fake Pearls Made from Tridacna gigas Shells Tanzania|Emerald from By Michael S. Krzemnicki and Laurent E. Cartier Ethiopia|Vivid purplish pink fluorite from Illinois, USA| 430 Large 12-Rayed Black Star Sapphire from Sri Lanka Colourless forsterite from with Asterism Caused by Ilmenite Inclusions Vietnam|Sapphire from By Thanh Nhan Bui, Pascal Entremont and Jean-Pierre Gauthier Ambatondrazaka, Madagascar| Colour-change scorodite from 436 Tsumeb, Namibia|Stichtite| Excursions Zoned type IaB/IIa diamond| Mogok, Myanmar: November 2016 Synthetic star ruby 444 Conferences AGA Tucson|GIT|Jewelry Industry Summit Cover Photo: High-quality rubies, sapphires 450 Letters and emeralds are typically ac- companied by geographical origin reports from gemmologi- 451 Gem-A Notices cal laboratories, as discussed on pp.
    [Show full text]
  • Kaersutite Naca2[(Mg; Fe )4Ti](Si6al2)O22(OH)2 C 2001 Mineral Data Publishing, Version 1.2 ° Crystal Data: Monoclinic
    2+ Kaersutite NaCa2[(Mg; Fe )4Ti](Si6Al2)O22(OH)2 c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Monoclinic. Point Group: 2=m: Commonly as well-formed phenocrysts with rhombic basal sections; prismatic, to 10 cm; as granular aggregates. Twinning: Simple or multiple twinning 100 . k f g Physical Properties: Cleavage: Perfect on 110 , intersecting at 56± and 124±; partings on 100 , 001 . Tenacity: Brittle. Hardness = 5f{6 gD(meas.) = 3.2{3.28 D(calc.) = [3.11] f g f g Optical Properties: Semitransparent. Color: Dark brown to black, typically zoned; yellow-brown, green-brown, or red-brown in thin section. Luster: Vitreous. Optical Class: Biaxial ({). Pleochroism: Strong; X = yellow, yellow-brown; Y = red, red-brown; Z = deep brown, dark red-brown. Orientation: Y = b; Z c = 0±{19±. Dispersion: r > v: Absorption: Z Y > X. ® = 1.670{1.689 ¯ = 1^.690{1.741 ° = 1.700{1.772 ¸ 2V(meas.) = 66±{82± Cell Data: Space Group: C2=m: a = 9.8903(3) b = 18.0596(5) c = 5.3152(2) ¯ = 105:4(1)± Z = 2 X-ray Powder Pattern: Boulder Dam area, Arizona, USA. (ICDD 17-478). 2.693 (100), 3.11 (80), 8.38 (65), 3.36 (65), 2.548 (65), 2.589 (55), 1.439 (55) Chemistry: (1) (2) (1) (2) SiO2 39.50 39.88 MgO 12.90 14.10 TiO2 10.33 4.69 CaO 10.91 13.05 Al2O3 11.12 14.25 Na2O 3.82 1.86 Fe2O3 0.06 9.58 K2O 1.43 1.80 FeO 9.44 0.10 F 0.14 + MnO 0.10 0.10 H2O 0.59 0.53 Total 100.20 100.08 2+ (1) Qaersut, Greenland; corresponds to (Na1:11K0:28)§=1:39Ca1:76(Mg2:89Fe1:19Ti1:17 3+ Fe0:01Mn0:01)§=5:27(Si5:93Al1:97)§=7:90O22(OH)0:59: (2) Vl·c¶³ Hora, Czech Republic; 3+ by microanalysis, corresponds to (Na0:53K0:41)§=0:94Ca2:06(Mg3:10Fe1:06Ti0:52Al0:34 2+ Fe0:01Mn0:01)§=5:04(Si5:87Al2:13)§=8:00O22[(OH)1:94F0:06]§=2:00: Polymorphism & Series: Forms a series with ferrokaersutite.
    [Show full text]
  • Some Gemological Challenges in Identifying Black Opaque Gem
    By Mary L.Johnson, Shane F, McClure, and Dino G. DeGhionno Among the most difficult gems to identi- ne of the most challenging problems in gemology is that fy are those that are black and opaque (or of determining the identity of a blaclz opaque gem inate- nearly so). In general, any gem material 0rial-hereafter called a "blaclz opaque." Such materials are can be opaque because of inclusions, any a mainstay of the jewelry business, primarily as side stones, dec- black opaque material can be fashioned, orative elements in multi-stone mosaics, and in men's jewelry. and any porous material can be dyed. Treated blaclz chalcedony ("black onyx"), black jade, and Thus, to identify a black opaque materi- al, every possible mineral, and many hematite traditionally have been the black opaques in greatest rocks and manufactured substances, demand. As a variety of quartz, "black onyx" is probably the must be considered. Microscopic appear- most familiar durable black opaque to lapidaries and gem cut- ance, refractive index, specific gravity, ters. Today, it is a popular medium for artistic carvings, many of and other properties (such as magnetism which have been incorporated into fine jewelry (figure 1). or radioactivity) provide useful clues, but In recent years, various materials have been misrepresent- in most cases advanced identification ed as "black onyx" or "black jade" to meet the trade's need for techniques (X-raydiffraction, EDXRF calibrated goods in high-volume markets. Members of the spectroscopy) are necessary, and even trade, in turn, have been sending samples to identification lab- these may not be conclusive.
    [Show full text]
  • Crystal-Chemistry and Short-Range Order Of
    Short-range order in fluoro-amphiboles CRYSTAL-CHEMISTRY AND SHORT-RANGE ORDER OF FLUORO-EDENITE AND FLUORO-PARGASITE: A COMBINED X-RAY DIFFRACTION AND FTIR SPECTROSCOPIC APPROACH 1,2 1,2 GIANCARLO DELLA VENTURA , FABIO BELLATRECCIA , FERNANDO 3 4 CÁMARA AND ROBERTA OBERTI 1) Dipartimento di Scienze, Università di Roma Tre, Largo S. Leonardo Murialdo 1, I-00146 Roma, Italy 2) INFN, Laboratori Nazionali di Frascati, Roma 3) Dipartimento di Scienze della Terra, via Valperga Caluso 35, I-10125 Torino 4) CNR-Istituto di Geoscienze e Georisorse, UOS Pavia, via Ferrata 1, I-27100 Pavia, Italy 1 Short-range order in fluoro-amphiboles ABSTRACT In this study we address the crystal-chemistry of a set of five samples of F-rich amphiboles from the Franklin marble (USA), using a combination of microchemical (EMPA), SREF, and FTIR spectroscopy methods. The EMPA data show that three samples fall into the compositional field of fluoro-edenite (Hawthorne et al., 2012), whereas two samples are enriched in high-charged C cations, and - although very close to the CR3+ boundary - must be classified as fluoro-pargasite. Mg is by far the dominant C cation, Ca is the dominant B cation (with BNa in the range 0.00-0.05 apfu, atoms per formula unit), and Na is the dominant A cation, with A (vacancy) in the range 0.07- 0.21 apfu; WF is in the range 1.18-1.46 apfu. SREF data show that: TAl is completely ordered at the T(1) site; the M(1) site is occupied only by divalent cations (Mg and Fe2+); CAl is disordered between the M(2) and M(3) sites; ANa is ordered at the A(m) site, as expected in F-rich compositions.
    [Show full text]