Benitoite from the New Idria District, San Benito
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WaTEn RESOURCESINVESTIGATIONS O'Brien and W J. Stone, 1984:Ground Water, Newpublications v.22, no. 6, pp.717-727. 83-4l18-B-Maps showing ground-water levels, Volcanogenic-exhalativetungsten mineralization springs, and depth to ground water, Basin and T{MBMMR of Proterozoic age near Santa Fe, New Mexico, Range Province, New Mexico, by B. T. Brady, *Circular L90--The skull of Sphenacodon and implicationsfor exploration,by M. S. Fulp ferocior, D. A. Mulvihill, D. L Hart, and W. H. Lan- and comoarisons with other sphenacodontines Jr., andJ.L. Renshaw,1985: Geology, v.73,pp.66- ger, 7984,6 pp., 2 sheets,scale 1:500,000 (ReptiliaiPelycosauria), by D.-A. Eberth, 1985, 69. 83-411.8-C-Maps showing distribution of dis- 39 pp., 2 tables, 39 figs $4.00 in Virtually complete, disarticulated cranial re- solved solids and dominant chemical type New 0pen-filereports ma\nsof Sohenacodonferociorfrom the Cutler and ground water, Basin and Range Province, and NMBMMR Abo Formations (Lower Permian) of north-cen- Mexico,by T. H. Thompson, R. Chappell, scale *215--Evaluation tral New Mexico are described in detail for the D. L. Hart, Jr., 7984, 5 pp., 2 sheets, of laboratory procedures for de- first time. These descriptions provide the basis 1:500,000. termining soil-water chloride, by B. E. McGurk for the most detailedcomparisons to datewithin 83-41.18-D-Map showing outcrops of granitic and W. f. Stone,1985, 36 pp., 12 tables,2 figs. and the subfamily Sphen- rocks and silicic shallow-intrusive rocks, Basin $7.20 the genus Sphenacodon *21.9-Geology acodontinae. -
Crystal Structure of Bage [Ge3 O9] and Its Relation to Benitoite
------------- ., JOURNAL OF RESEARCH of the National Bureau of Standards - A. Physics and Chemistry Vol. 70A, No.5, September-October 1966 Crystal Structure of BaGe [ Ge3 0 9 Jand Its Relation to Benitoite I I C. Robbins, A. Perloff, and S. Block ~ ( Institute for Materials Research, National Bureau of Standards, Washington, D.C. 20234 I (May 23, 1966) BaGe[Ge30gl is trigonal, space group P3, with lattice constants a= 11.61, c=4.74 A, and Z =3. The structure was established by three·dimensional Patterson and electron density syntheses. Three·dimensional least·squares refinement resulted in a final R value of 6.8 percent (observed data only). The previously proposed structural relationship of this compound with benitoite, BaTiSbOg, has been confirmed. The structure can be considered as composed of Ge30g rings, in which the Ge is tetrahedrally coordinated, linked through octahedrally coordinated Ge atoms to form a three·dimen· sional Ge·O network. All Ge polyhedra are linked by corner sharing. The Ba ions occupy positions in channels of the network. Key Words: Barium tetragermanate, structure, benitoite, crystal, x·ray. 1. Introduction Robbins and Levin [lJ. Their data plus the space group information are: The synthesis of three germanates of formula type MeGe4 0g (Me = Sr, Pb, Ba) was reported by Robbins a=lL61 A w= L797±0.003 and Levin [lJ .1 A comparison of indexed powder c=4.74A E= 1.783 ± 0.003 patterns suggested that the compounds were isostruc S.G.=P3 p (obs) = 5.1 gcm - 3 turaL This was later confirmed by Eulenberger, Z =3 p (calc) = 5.12 gcm- 3 Wittman, and Nowotny [2]. -
List of New Mineral Names: with an Index of Authors
415 A (fifth) list of new mineral names: with an index of authors. 1 By L. J. S~v.scs~, M.A., F.G.S. Assistant in the ~Iineral Department of the,Brltish Museum. [Communicated June 7, 1910.] Aglaurito. R. Handmann, 1907. Zeita. Min. Geol. Stuttgart, col. i, p. 78. Orthoc]ase-felspar with a fine blue reflection forming a constituent of quartz-porphyry (Aglauritporphyr) from Teplitz, Bohemia. Named from ~,Xavpo~ ---- ~Xa&, bright. Alaito. K. A. ~Yenadkevi~, 1909. BuU. Acad. Sci. Saint-P6tersbourg, ser. 6, col. iii, p. 185 (A~am~s). Hydrate~l vanadic oxide, V205. H~O, forming blood=red, mossy growths with silky lustre. Founi] with turanite (q. v.) in thct neighbourhood of the Alai Mountains, Russian Central Asia. Alamosite. C. Palaehe and H. E. Merwin, 1909. Amer. Journ. Sci., ser. 4, col. xxvii, p. 899; Zeits. Kryst. Min., col. xlvi, p. 518. Lead recta-silicate, PbSiOs, occurring as snow-white, radially fibrous masses. Crystals are monoclinic, though apparently not isom0rphous with wol]astonite. From Alamos, Sonora, Mexico. Prepared artificially by S. Hilpert and P. Weiller, Ber. Deutsch. Chem. Ges., 1909, col. xlii, p. 2969. Aloisiite. L. Colomba, 1908. Rend. B. Accad. Lincei, Roma, set. 5, col. xvii, sere. 2, p. 233. A hydrated sub-silicate of calcium, ferrous iron, magnesium, sodium, and hydrogen, (R pp, R',), SiO,, occurring in an amorphous condition, intimately mixed with oalcinm carbonate, in a palagonite-tuff at Fort Portal, Uganda. Named in honour of H.R.H. Prince Luigi Amedeo of Savoy, Duke of Abruzzi. Aloisius or Aloysius is a Latin form of Luigi or I~ewis. -
Initial Study / Mitigated Negative Declaration City of Hollister San Benito River Greenway
INITIAL STUDY / MITIGATED NEGATIVE DECLARATION CITY OF HOLLISTER SAN BENITO RIVER GREENWAY DECEMBER 2008 Lead Agency: City of Hollister Engineering Department 375 Fifth Street Hollister, CA 95024 Prepared By: Analytical Environmental Services 1801 7th Street, Suite 100 Sacramento, Ca 95811 INITIAL STUDY / MITIGATED NEGATIVE DECLARATION CITY OF HOLLISTER SAN BENITO RIVER GREENWAY DECEMBER 2008 Lead Agency: City of Hollister Engineering Department 375 Fifth Street Hollister, CA 95024 Prepared By: Analytical Environmental Services 1801 7th Street, Suite 100 Sacramento, Ca 95811 TABLE OF CONTENTS SAN BENITO RIVER GREENWAY PROJECT INITIAL STUDY / MITIGATED NEGATIVE DECLARATION 1.0 INTRODUCTION ........................................................................................................................... 1-1 1.1 Purpose of Study ............................................................................................................... 1-1 1.2 Environmental Factors Potentially Affected ....................................................................... 1-1 1.3 Evaluation Terminology ..................................................................................................... 1-1 1.4 Organization of the Initial Study ......................................................................................... 1-2 2.0 PROJECT DESCRIPTION ............................................................................................................ 2-1 2.1 Introduction ....................................................................................................................... -
Mineralogicai, Radiographic and Uranium Leaching Studies on the Uranium Ore from Kvanefjeld, Ilimaussaq Complex, South Greenland
T><2too/t6' Risø-R-416 Mineralogicai, Radiographic and Uranium Leaching Studies on the Uranium Ore from Kvanefjeld, Ilimaussaq Complex, South Greenland Milota Makovicky, Emil Makovicky, Bjarne Leth Nielsen, Svend Karup-Møller, and Emil Sørensen Risø National Laboratory, DK-4000 Roskilde, Denmark June 1980 RISØ-R-416 MINERALOGICAL, RADIOGRAPHIC AND URANIUM LEACHING STUDIES ON THE URANIUM ORE FROM KVANEFJELD, ILIMAUSSAQ. COMPLEX, 'SOUTH GREENLAND Milota Makovickyl , Emil Makovicky2, Bjarne Leth Nielsen-! , Sven Karuo-Møller^ and Emil Sørensen^ Abstract. 102 samples of low-grade uranium ore from 70 drill holes at Kvanefjeld, Ilimaussaq alkaline intrusion, South Green land were studied by means of autoradiography, fission-track investigations, microscopy, microprobe analyses and uranium- leaching experiments. The principal U-Th bearing mineral, steen- strupine, and several less common uranium minerals are dis seminated in lujavrite 'nepheline syenite) and altered volcanic rocks. Stenstrupine has a/erage composition Na6.7HxCai.n e Al (REE+Y)5.8(Th,l')o.5 ( ""1 . 6*" 1 . S^Q. 3^0. l 0. 2 ) Sii2036 (P4.3Si-) ,7 )024 (F,OH). nH20; n and x are variable. It either is of magmatic origin (type A) or connected with metasomatic processes (type B), or occurs in late veins (Type C). Preponder ance of grains are metamict (usually 2000-5000 ppm U3O8) or al tered (usually above 5000 ppm U3O8), sometimes zoned with both (continue on next page) June 1980 Pisø National Laboratory, DK-4000 Roskilde, Denmark components present. Occasionally they are extremely altered with U content falling to 500-5000 ppm U3O8 and local accumulations of high-U minerals formed. -
Reflective Index Reference Chart
REFLECTIVE INDEX REFERENCE CHART FOR PRESIDIUM DUO TESTER (PDT) Reflective Index Refractive Reflective Index Refractive Reflective Index Refractive Gemstone on PDT/PRM Index Gemstone on PDT/PRM Index Gemstone on PDT/PRM Index Fluorite 16 - 18 1.434 - 1.434 Emerald 26 - 29 1.580 - 1.580 Corundum 34 - 43 1.762 - 1.770 Opal 17 - 19 1.450 - 1.450 Verdite 26 - 29 1.580 - 1.580 Idocrase 35 - 39 1.713 - 1.718 ? Glass 17 - 54 1.440 - 1.900 Brazilianite 27 - 32 1.602 - 1.621 Spinel 36 - 39 1.718 - 1.718 How does your Presidium tester Plastic 18 - 38 1.460 - 1.700 Rhodochrosite 27 - 48 1.597 - 1.817 TL Grossularite Garnet 36 - 40 1.720 - 1.720 Sodalite 19 - 21 1.483 - 1.483 Actinolite 28 - 33 1.614 - 1.642 Kyanite 36 - 41 1.716 - 1.731 work to get R.I. values? Lapis-lazuli 20 - 23 1.500 - 1.500 Nephrite 28 - 33 1.606 - 1.632 Rhodonite 37 - 41 1.730 - 1.740 Reflective indices developed by Presidium can Moldavite 20 - 23 1.500 - 1.500 Turquoise 28 - 34 1.610 - 1.650 TP Grossularite Garnet (Hessonite) 37 - 41 1.740 - 1.740 be matched in this table to the corresponding Obsidian 20 - 23 1.500 - 1.500 Topaz (Blue, White) 29 - 32 1.619 - 1.627 Chrysoberyl (Alexandrite) 38 - 42 1.746 - 1.755 common Refractive Index values to get the Calcite 20 - 35 1.486 - 1.658 Danburite 29 - 33 1.630 - 1.636 Pyrope Garnet 38 - 42 1.746 - 1.746 R.I value of the gemstone. -
PABSTITE from the DARA-I-PIOZ MORAINE (TADJIKISTAN)
New data on minerals. M.: 2003. Volume 38 UDC 549.6 PABSTITE FROM THE DARA-i-PIOZ MORAINE (TADJIKISTAN) Leonid A. Pautov Fersman Mineralogical Museum of the Russian Academy of Science. Moscow, [email protected] Pabstite was discovered in the moraine of the Dara-i-Pioz glacier (Garmsky district, Tadjikistan) in a leuco- cratic rock mainly composed of microcline, quartz, and albite. Subordinated minerals are aegirine, titanite, astrophyllite, bafertisite, galena, sphalerite, ilmenite, pyrochlore, fluorite, zircon, fluorapatite, and calcite. Pabstite forms grains and well-faced crystals (0.1-0.5 mm), growing on quartz crystals in small cavities abun- dant in the rock. Its composition is close to the final member BaSnSi:P9 in the series pabstite-benitoite. Microprobe analysis has shown: SiO, - 37.43; Ti02 - 0.19; Zr02 - 0.16; Sn02 - 30.05; BaO - 32.41; total 100.24. The empirical formula is Balo2(Sno96Tio.01Zroo,)o98Si3o,09'Refraction parameters of pabstite are no = 1.668(2); 1.657(2), which is much lower than cited figures for pabstite from the type locality. Strong n" = dependence of pabstite optical properties on titanium contents is shown. The find of pabstite at Dara-i-Pioze is the first find of pabstite in alkaline rocks and, apparently, the second find of this mineral in the world. 2 tables, 3 figures and 13 references. Pabstite BaSnSi30g, the tin analogue of beni- aegirine syenites and foyaites. The first data on toite, was described as a new mineral from the massif were received at works of Tadjik- Santa Cruz (California, USA), where it was met Pamirs expedition of 1932 - 1936. -
Mangan-Neptunite Kna2li(Mn2+,Fe2+)
2+ 2+ Mangan-neptunite KNa2Li(Mn ; Fe )2Ti2Si8O24 c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Monoclinic. Point Group: 2=m or 2: Crystals prismatic, somewhat elongated along [001], to 7 cm, showing 110 , 001 , 100 , also 111 , 111 , rare 210 . Also as aggregates of small crystals, druses, rofsettges,fbloogmsf, andg earthfy crugstsf. Tgwinninfg: Ags contact twins on 001 . f g Physical Properties: Cleavage: Distinct in two directions, intersecting at 80 . » ± Fracture: Uneven to conchoidal. Tenacity: Brittle. Hardness = 5{6 D(meas.) = 3.17{3.20 D(calc.) = 3.26 Optical Properties: Transparent to translucent to opaque. Color: Dark cherry-red, orange, or black in small crystals; cherry-red in thin fragments; in thin section, light yellow, orange, or red-orange. Streak: Brick-red to reddish brown. Luster: Vitreous to resinous. Optical Class: Biaxial (+). Pleochroism: Distinct; X = light yellow; Y = orange or yellow-orange; Z = red-orange. Orientation: Y = b; Z c = 16 {20 . Dispersion: r < v; ^ ± ± very strong. Absorption: Z > Y > X. ® = 1.691{1.697 ¯ = 1.693{1.700 ° = 1.713{1.728 2V(meas.) = 31±{36± Cell Data: Space Group: C2=m or C2=c: a = 16.38 b = 12.48 c = 10.01 ¯ = 115±240 Z = 4 X-ray Powder Pattern: Lovozero massif, Russia. 2.485 (100), 1.506 (100), 1.483 (90), 2.170 (80), 1.924 (70), 2.841 (60), 2.948 (50) Chemistry: (1) (2) (3) (1) (2) (3) SiO2 52.65 52.68 52.98 CaO 0.37 0.43 TiO2 17.38 18.21 17.61 Li2O 1.08 1.65 Al2O3 0.99 Na2O 5.12 9.16 6.83 Fe2O3 1.07 K2O 6.30 4.94 5.19 + FeO 5.54 5.16 7.92 H2O 0.06 MnO 8.87 9.95 7.82 H2O¡ 0.10 MgO 0.15 0.12 Total 99.68 100.65 100.00 (1) Mt. -
RARE EARTHS in MINERALS of the JOAQUINITE GROUP E. I. Sblrbnov,Lv
THE AMERICAN MINERALOGIST, VOL. 52, NOVEMBER-DECEMBER, 1967 RARE EARTHS IN MINERALS OF THE JOAQUINITE GROUP E. I. SBlrBNov,lV. f. Buxrw,2YU. A. Ber.Asuov,2aNr H. SdnnNsBuB ABsrRAcr An apparently new rare-earth mineral of the joaquinite group occurs in nephelin-syenite pegmatites of Ilimaussaq alkaline massif (S. Greenland). Optical and X-ray properties are the same, as for standard joaquinite NaBaTirSirOrs from California, but the chemical analysis is quite difierent: SiO, 33.82, NbzOs 2.31, TiO29.20, Feror 0.39, FeO 4.78, MnO 0.70, ThOz 0.38, RErOs 22.59, BaO 21.46, (Ca, Sr)O 0.03, Na:O 2.41, KzO 0.22, HzO 1.50, F 0 38, -O:F2-0.16, sum 100.01.The formula is NaBa2Fe2+CezTi:SisOr6(OH)(Z:4). Semiquantitative analyses of California joaquinite also showed the presence of consider- able rare earths. INrnooucrroN During summer field work (1964) in the expedition of the Greenland Geological Survey, headed by H. Sfrensen, in the Ilimaussaq alkaline massif (S. Greenland), E. L Semenov found an unknown mineral of composition NaBarFeCezTi2Si8O26(OH)containing 2370 F.E1o3in the nepheline syenite pegmatites. At present no barium-titanium silicate minerals containing rare earths are known. However, the Soviet Com- mission on New Minerals observed the similarity of unit cell dimensions and optical affinities of this mineral with joaquinite, NaBa(Ti,Fe)aSiaOrr,, for which the content of rare earths was not shown in analyses.Therefore both minerals were studied. Joaquinite has been described from San Benito County, California (Palacheand Foshag,1932), and from SealLake, Quebec,Canada (Bell, 1963).One California specimen(No. -
Chapter 8 Natural Resources
CHAPTER 8. NATURAL RESOURCES San Benito County General Plan Chapter 8 Natural Resources This chapter describes the location and extent of existing natural resources within San Benito County, including water resources, mineral and energy resources, biological resources, and oil and gas resources. This chapter is organized into the following sections: . Water Resources (Section 8.1) . Energy and Mineral Resources (Section 8.2) . Biological Resources (Section 8.3) . Oil and Gas Resources (Section 8.4) Public Draft Background Report Page 8-1 November 2010 CHAPTER 8. NATURAL RESOURCES San Benito County General Plan This page is intentionally left blank. Page 8-2 Public Review Draft Background Report November 2010 CHAPTER 8. NATURAL RESOURCES San Benito County General Plan SECTION 8.1 WATER RESOURCES Introduction This section summarizes and analyzes information about the availability and quality of water resources in San Benito County. It includes information about historical and current conditions and projections for future ground water, surface water, and imported water resource conditions, where available. Analyzing existing water resource conditions and water supply data provides important information about the ability of the County to provide and manage water supplies that meet both existing and projected future growth. Key Terms Acre-foot (AF). The volume of water required to cover one acre of land (43,560 square feet) to a depth of one foot. One acre-foot is equal to 325,851 gallons or 1,233 cubic meters. Historically, an acre-foot represents the amount of water typically used by one family during a year. Aquifer. A geological formation or structure that stores and/or transmits water, such as wells and springs. -
TUGTUPITE: a GEMSTONE from GREENLAND by Aage Jensen and Ole V
TUGTUPITE: A GEMSTONE FROM GREENLAND By Aage Jensen and Ole V. Petersen The red variety of the mineral tugtupite, a rare is derived from the locality where the mineral silicate closely related to sodalite, has been used as was first found. In 1965, the Commission on New a gemstone since 1965. This article presents the Minerals and Mineral Names of the International history of the mineral and details of its mineralogy Mineralogical Association approved both the and gemology. A recently discovered light blue mineral and the name. variety of tugtupite is also described. Thus far, Dan0 (1966) described the crystal structure of tugiupite has been found in only two localities: (1) tugtupite. A detailed description of the crystal Lovozero, Kola Peninsula, U.S.S.R., where it occurs as very small1 grains; and (2) Ilimaussaq, South habit, the pseudocubic penetration trillings, and Greenland, where it has been located at several the numerous localities where tugtupite had been places within the Ilimaussaq intrusion. Gem-quality found from the time that it was first traced at tugtupite has come almost exclusively from one Tugtup agtalzorfia until 1971 (including the only occurrence, a set of hydrothermal albite veins from one that has produced gem material of any sig- the Kvanefjeld plateau in the northwestern corner of nificance) was presented by S0rensen et al. (1971). the Ilimaussaq intrusion. Another type of twin, pseudotrigonal contact trillings, was subsequently described by Petersen (19781. The tugtupite from the type locality was The mineral that is now known as tugtupite was described as white, but Sflrensen (1960)mentions discovered in 1957 by Professor H. -
Second Order P6c2-P31c Transition and Structural
American Mineralogist, Volume 97, pages 1749–1763, 2012 Second-order P6c2-P31c transition and structural crystallography of the cyclosilicate benitoite, BaTiSi3O9, at high pressure CLIVIA HEJNY,1,* RONALD MILETICH,2 ANDREAS JASSER,3 PASCAL SCHOUWINK,3,4 WILSON CRICHTON,5 AND VOLKER KAHLENBERG1 1Institut für Mineralogie und Petrographie der Universität Innsbruck, Innrain 52, 6020 Innsbruck, Austria 2Institut für Mineralogie und Kristallographie der Universität Wien, Althanstrasse 14, 1090 Wein, Austria 3Institut für Geowissenschaften der Universität Heidelberg, Im Neuenheimer Feld 234, 69120 Heidelberg, Germany 4Laboratoire de Cristallographie de l’Université de Genève, 24, quai Ernest-Ansermet, 1211 Geneva 4, Switzerland 5European Synchrotron Radiation Facility, ESRF, 6 Rue Jules Horowitz, 38043 Grenoble, France ABSTRACT Experimental high-pressure investigations on benitoite in the diamond-anvil cell reveal a second- order phase transition at a critical transition pressure Pc = 4.24(3) GPa, as determined from synchrotron powder diffraction, single-crystal X-ray diffraction, and Raman spectroscopy. Diffraction experiments indicate a non-isomorphous transition from P6c2 to P31c space-group symmetry with a′ = a√3 and c′ = c relative to the P62c subcell below Pc. The high-pressure polymorph is characterized by a larger compressibility compared to the compressional behavior of benitoite below Pc. Fitting second-order Birch-Murnaghan equations of state to the experimental data sets, the parameters obtained are V0 = 3 372.34(4) Å , K0 = 117.9(7) GPa, with a0 = 6.6387(3) Å, Ka = 108.1(7) GPa, and c0 = 9.7554(4) Å, Kc 3 = 143.3(1.1) GPa for the low-pressure form (P < Pc), and V0 = 376.1(4) Å , K0 = 88.9(1.6) GPa, with a0 = 11.516(4) Å, Ka = 95.4(1.8) GPa, and c0 = 9.826(4) Å, Kc = 77.2(1.6) GPa for the high-pressure form (P > Pc).