Mineralogy Chkalovite
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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. -
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. -
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. -
The Crystal Structure of Cascandite, Cascsi30s(OH)
--~~-- American Mineralogist, Volume 67, pages 604-609, 1982 The crystal structure of cascandite, CaScSi30S(OH) MARCELLO MELLINI AND STEFANO MERLINO Istituto di Mineralogia e Petrografia, Universita di Pisa and C.N.R., C.S. Geologia Strutturale e Dinamica dell'Appennino via S. Maria 53, 56100 Pisa, Italy Abstract A new pyroxenoid mineral, cascandite, with the ideal formula CaScSi308(OH), is 9.791(8)A, b = 10.420(9)A, c = 7.076(6)A, a = 98.91(8)°,13 = 102.63(8)°, triclinic with a = 'Y = 84.17(8)°; Z = 4 for the cT unit cell setting. The crystal structure of cascandite is similar to those of pectolite and serandite and is composed of two main structural units: octahedral chains and three-repeat tetrahedral chains. Cascandite, unlike pectolite and serandite, has only two octahedral cations per formula unit, and the octahedral chains are formed by two strands of edge-sharing octahedra occupied by calcium and scandium cations. Cascandite is a member of the hydrous pyroxenoid series, whose peculiarities are related to the presence of intrachain hydrogen bonding. Introduction obtained starting from the atomic coordinates of Cascandite, a new scandium silicate, was found wollastonite based on pI setting, as given by in a geode from the granite of Baveno, Italy, Buerger and Prewitt (1961). However the E statis- together with quartz, orthoclase, albite and jervi- tics indicated a non-centro symmetric structure, and site, another new scandium silicate with ideal for- thus we removed the symmetry constraints on the mula NaScSiz06. The descriptions of these new octahedral cations. We assumed that one of the six minerals are given by Mellini et ale (1982). -
COMPARISON of the CRYSTAL STRUCTURES of BUSTAMITE and WOLLASTONITE Dowarn R
THE AMERICAN MINERALOGIST, VOL. 48, MAY-JUNE, 1963 COMPARISON OF THE CRYSTAL STRUCTURES OF BUSTAMITE AND WOLLASTONITE Dowarn R. Pneconl,q.Nl C. T. Pnnwrrr,2Massachusetts I nslituteof T echnology, Cambrid ge, M ass achus etts Aesrnecr The structures of bustamite and wollastonite difier principally only in the relative arrangement of chains of tetrahedra. Both structures have a pseudomonoclinic cell, this unit having space group P21/rnin wollastonite and A2/m in bustamite. INrnooucrtoN On the basis of a comparisonof optical properties, Sundius (1931) postulatedthat bustamite (CaMnSizOo)is Mn-rich wollastonite(CaSiOa). Schaller(1938, 1955) also concluded that bustamite had the wollastonite structure becauseof a closerelationship between the optical propertiesof the two minerals. Berman and Gonyer (1937), using rotating-crystal Tasln 1. Syuunrnv ,rNo Ulrrr-cnr-r Dere lon Busr.qurre aun Wolr-lsroNrrB Woliastonite Bustamite Peacor Bustamite Peacor Buerger and Buerger and Prewitt 7.e4A r5.4r2L 7.rc6L b 7.32 7.157 7.r57 7.07 13.824 13.824 q 90"02' 89"29' 90031' R 95"22', 9405r1 9+"35', ^l 103026' I0zo56' t03"52', Space group PI FI A1 photographs, found that their unit cells were similar, and concluded that they wererelated only by solid solution.Buerger, however, (1956) found that the unit cell of bustamite (Table 1) is closelyrelated to, but different from, the cell of wollastonite. He noted that there is a sort of super- structure relation between the two minerals. Liebau et al. (1958) con- firmed Buerger's unit cell and guessedthat the differencein structures is basedonly on a different ordering of chains and cations. -
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. -
ON the CRYSTALLOGRAPHY of AXINITE and the NORMAL SETTING of TRICLINIC CRYSTALS MA Pracock, Harvard
ON THE CRYSTALLOGRAPHY OF AXINITE AND THE NORMAL SETTING OF TRICLINIC CRYSTALS M. A. PracocK, Harvard.(Iniaersity, Cambriilge, Mass. CoNrBNrs Present Status of the Problem of Choosing Morphological Elements. 588 Course of the Present Study 591 Several Steps in Choosing Normal Triclinic Elements. 592 Determination of the SpecificLattice ... ... 592 Choice oI the Represbntative Lattice Cell .. 593 Orientation of the Representative Lattice Cell. 593 Determination of Normal Elements from the External Geometry 597 Determination of Normal Elements from X-Ray Measurements 599 Relation of the New Lattice Elements to those of Cossner & Reicliel... 602 Determination of the Optical Elements 603 Definitive Presentation of the Crystallography of Axinite 605 Some of the Existing Settings of Axinite and the Underlying Principles. 605 Neumann (1825). 605 L6vy (1838)-Des Cloizeaux (1862).. 609 Miller (1852) 609 Vom Rath (1866). 610 Schrauf (1870). 6tL Goldschmidt(1886; 1897-19tJ) .. 612 Dana (1892) 613 Friedel (1926). 613 Propriety of the Normal Setting of Triclinic Crystals. 615 Summary.... 616 Acknowledgments. 617 References...... 618 ExplanationoftheFigures.....'Co-ordinate. .618 Appendix: Transformation of tf. O. H. DoNNev;... 62l PnBsBNr Srarus or.TrrE Pnonr-nu oF CHoosrNG MonpnorocrcAl ELEMENTS The problem of choosing morphological crystallographic elements reachesfull generality in the triclinic system, in which the mutual inter- sectionsof any three non-tautozonal crystal planes may be taken as axes of referencewith the intercepts of any crystal plane cutting all the axes to define the parameters. If the indices of the observed planes are to be small numbers only a moderate number of morphological lattices come under consideration; but since a triclinic lattice may be defined by any one of numerous cells, and any triclinic cell can be oriented in twenty- four different ways, the number of sets of geometrical elements that can be chosen for any one triclinic speciesis still very considerable. -
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. -
Villiaumite Naf C 2001-2005 Mineral Data Publishing, Version 1
Villiaumite NaF c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Cubic. Point Group: 4/m 32/m. Crystals rare, cubic, to 15 cm, may show {111}, {hll}, {hkl}; commonly granular, massive. Physical Properties: Cleavage: {001}, perfect. Tenacity: Brittle. Hardness = 2–2.5 D(meas.) = 2.79 D(calc.) = 2.808 Soluble in H2O; dark red to orange and yellow fluorescence under SW and LW UV. Optical Properties: Transparent. Color: Carmine-red, lavender-pink to light orange. Streak: White. Luster: Vitreous. Optical Class: Isotropic; weak anomalous anisotropism, then uniaxial (–). Pleochroism: Strong; E = yellow; O = pink to deep carmine. n = 1.327–1.328 Cell Data: Space Group: Fm3m (synthetic). a = 4.6342 Z = 4 X-ray Powder Pattern: Synthetic. 2.319 (100), 1.639 (60), 1.338 (17), 1.0363 (12), 0.9458 (8), 1.1588 (7), 2.680 (3) Chemistry: (1) (2) (3) Na 53.4 53.83 54.75 K trace 0.32 Mg trace Ca 1.2 ZrO2 1.5 F 44.2 45.28 45.25 insol. 0.84 Total 100.3 100.27 100.00 (1) Los Islands, Guinea. (2) Lovozero massif, Russia. (3) NaF. Occurrence: In nepheline syenite and nepheline syenite pegmatites; in lake-bed deposits. Association: Aegirine, sodalite, nepheline, neptunite, lamprophyllite, pectolite, serandite, eudialyte, ussingite, chkalovite, zeolites. Distribution: On Rouma Isle, Los Islands, Guinea. On Mts. Karnasurt and Alluaiv, Lovozero massif, and from the Khibiny massif, Kola Peninsula, Russia. At Kvanefjeld, Il´ımaussaqintrusion, Greenland. From Aris, about 20 km south of Windhoek, Namibia. At Lake Magadi, Kenya. From Po¸cosde Caldas, Minas Gerais, Brazil. -
Marshallsussmanite’ with a Reinstatement of the Name Schizolite Mncamnsi3o8(OH)
Discreditation of the pyroxenoid mineral name ‘marshallsussmanite’ with a reinstatement of the name schizolite MnCaMnSi3O8(OH) Joel D. Grice1*, Aaron J. Lussier1, Henrik Friis2, Ralph Rowe1, Glenn G. Poirier1 and Zina Fihl3 1Canadian Museum of Nature, PO Box 3443 Stn D, Ottawa Canada, KIP 6P4, Canada 2Natural History Museum, University of Oslo, PO Box 1172, Blindern, 0318 Oslo, Norway 3Natural History Museum of Denmark, Øster Volgade 5-7, 1350 Copenhagen K, Denmark *corresponding author; E-mail: [email protected] ABSTRACT Schizolite, originating from the type locality, Tutop Agtakôrfia, in the Ilímaussaq alkaline complex, Julianehåb district, South Greenland, was initially described by Winther (1901) with additional data being supplied by Bøggild (1903). Recently, a proposal for the new mineral ‘marshallsussmanite’ was submitted to, and approved by, the International Mineralogical Association - Commission on New Minerals, Nomenclature, and Classification (IMA 2013-067) by Origlieri et al. (2013). Results from the detailed examination of two schizolite cotype samples presented here, using single-crystal XRD, powder XRD, and optics, confirms it be equivalent to ‘marshallsussmanite’. Historical precedence sets a priority for discrediting the name ‘marshallsussmanite’ in favour of the original, more-than-a century-old name, This is a 'preproof' accepted article for Mineralogical Magazine. This version may be subject to change during the production process. DOI: 10.1180/mgm.2019.21 schizolite. The two schizolite samples investigated vary slightly in physical and chemical properties but are consistent overall. The prismatic crystals are pale red or pink to brownish. Schizolite is brittle with a splintery aspect. It is biaxial positive, with average optical parameters: α = 1.626 ± 0.003, β = 1.630 ± 0.002, γ = 1.661 ± 0.002, 2Vmeas = 71(4)º and 2Vcalc = 40º; there is no pleochroism. -
Diamond Dan's Mineral Names Dictionary
A Dictionary of Mineral Names By Darryl Powell Mineral Names What do they mean? Who created them? What can I learn from them? This mineral diction‐ ary is unique because it is illustrated, both with mineral drawings as well as pictures of people and places after which some minerals are named. The people pictured on this page have all made a con‐ tribution to what is formally called “mineral nomenclature.” Keep reading and you will discover who they are and what they did. In 1995, Diamond Dan Publications pub‐ lished its first full book, “A Mineral Collector’s Guide to Common Mineral Names: Their Ori‐ gins & Meanings.” Now it is twenty years later. What you will discover in this issue and in the March issue is a re‐ vised and improved version of this book. This Mineral Names Dictionary contains mineral names that the average mineral collector will encounter while collecting minerals, attending shows and visiting museum displays. In addition to the most common min‐ eral names, there are some unofficial names which you will still find on labels. Each mineral name has a story to tell or a lesson to teach. If you wanted to take the time, each name could become a topic to study. Armalcolite, for example, could quickly be‐ come a study of a mineral, first discovered on the moon, and brought back to earth by the astronauts Armstrong, Aldrin and Collins (do you see parts of their names in this mineral name?) This could lead you to a study of American astronauts landing on the moon, what it took to get there and what we discovered by landing on the moon.