Parting Shots
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Karl Ludwig Giesecke
73 Karl Ludwig Giesecke (1761 – 1833) Zur Erinnerung an den Augsburger Theaterdichter, Forschungsreisenden und Mineralogen Gerd Ibler Kryolith von Ivigtut (Ivittuut), Südgrönland. Kryolith von Ivigtut (Ivittuut), Südgrönland. Augsburg. Gerd Ibler/Richard Speckmeier, Foto: Vor 250 Jahren, am 6. April 1761, wurde Giesecke nennen sollte, und mit diesem in Augsburg Johann Georg Metzler gebo- Pseudonym als Theaterdichter und Mine- ren, der sich als 20-Jähriger Karl Ludwig raloge Geschichte machte. Herkunft und Ausbildung Sein Vater, Johann Georg Metzler, ein Anwesen „Bei den sieben Kindeln“ in der Schneidermeister aus Edelfingen in Würt- Augsburger Altstadt befindet. Der jun- temberg, war mit Sibylla Magdalena Götz ge Metzler besuchte das Humanistische aus Augsburg verheiratet. Die Mutter Gymnasium St. Anna, wo er 1781 sein schenkte insgesamt 15 Kindern das Leben. Abi tur ablegte. Danach war er Student der Johann Georg Metzler alias Karl Ludwig Rechte an der Georg-August-Universität Giesecke war der zweitgeborene Sohn. Er in Göttingen und wurde vom 1.11.1781 wurde in St. Jacob evangelisch getauft. Die bis Michaelis 1783 mit einem Stipendium Familie Metzler bewohnte ab 1763 das des evangelischen Scholarchats des Augs- Haus H 375, das heutige Haus „Mittlerer burger Gymnasiums Annaneum unter- Graben Nr. 30“, das sich gegenüber dem stützt. Naturhistorica BERICHTE DER NATURHISTORISCHEN GESELLSCHAFT HANNOVER 153 · 2011 74 Gerd Ibler Metzler/Giesecke als Schauspieler und Dichter Johann Georg Metzler brach plötzlich Muttersöhnchen auf der Galeere oder man sein Studium ab und wurde nicht Jurist, trägt den Krug solange zum Brunnen, bis sondern begeisterte sich für das Theater. Er er bricht“. tingelte als Schauspieler unter dem Künst- Als Journalist und Chronist des Thea- lernamen Karl Ludwig Giesecke mit ver- terlebens hat Giesecke sich in Regensburg schiedenen Wanderbühnen von Bremen, von 1784 bis 1786 und in Salzburg von Pyrmont, Köln, Bonn, Mainz, Frankfurt/ 1786 bis 1787 hervorgetan und zwei Thea- Main über Regensburg, Augsburg, Salz- terjournale geschrieben. -
Geology and Age of the Lac a La Perdrix Fenite, Southern Gatineau District, Quebec
CA9700383 -4- Geology and age of the Lac a la Perdrix fenite, southern Gatineau district, Quebec D.D. Hogarth1 and Otto van Breemen2 Hogarth, D.D. and van Breemen, 0., 1996: Geology and age of the Lac a la Perdrix fenite, southern Gatineau district, Quebec; inRadiogenic Age and Isotopic Studies: Report 9; Geological Survey of Canada, Current Research 1995-F, p. 33-41. Abstract: The Lac a la Perdrix fenite lies in the Central Metasedimentary Belt of the Grenville Province. This 30 m wide fenite, adjacent to a narrow calciocarbonatite sill, replaces diopside-oligoclase gneiss and is composed of magnesio-arfvedsonite, aegirine, microcline, albite, and fluorapatite. Near the contact with carbonatite, it contains appreciable monazite and barite whereas aegirine virtually disappears. Fenitization probably took place early in the igneous stage of carbonatite development. A Pb/U monazite age of 1026 ± 2 Ma is thought to date fenite formation. Together with published data, this age shows that carbonatite intruded metamorphic rocks near the close of the Grenville Orogeny. Resume : La fenite de Lac a la Perdrix s'observe dans la ceinture metasedimentaire de la Province de Grenville. Cette fenite, mesurant 30 m de largeur et en position adjacente par rapport a un etroit filon-couche de calciocarbonatite, remplace un gneiss a diopside-oligoclase et se compose de magnesio-arfvedsonite, d'aegirine, de microcline, d'albite et de fluorapatite. Pres du contact avec la carbonatite, la fenite contient de la monazite et de la barytine en quantite appreciable, tandis que l'aegirine disparait pratiquement. La fenitisation a probablement eu lieu au debut de l'episode igne durant lequel s'est form6 la carbonatite. -
Chemical Composition and Petrogenetic Implications of Eudialyte-Group Mineral in the Peralkaline Lovozero Complex, Kola Peninsula, Russia
minerals Article Chemical Composition and Petrogenetic Implications of Eudialyte-Group Mineral in the Peralkaline Lovozero Complex, Kola Peninsula, Russia Lia Kogarko 1,* and Troels F. D. Nielsen 2 1 Vernadsky Institute of Geochemistry and Analytical Chemistry, Russian Academy of Sciences, 119991 Moscow, Russia 2 Geological Survey of Denmark and Greenland, 1350 Copenhagen, Denmark; [email protected] * Correspondence: [email protected] Received: 23 September 2020; Accepted: 16 November 2020; Published: 20 November 2020 Abstract: Lovozero complex, the world’s largest layered peralkaline intrusive complex hosts gigantic deposits of Zr-, Hf-, Nb-, LREE-, and HREE-rich Eudialyte Group of Mineral (EGM). The petrographic relations of EGM change with time and advancing crystallization up from Phase II (differentiated complex) to Phase III (eudialyte complex). EGM is anhedral interstitial in all of Phase II which indicates that EGM nucleated late relative to the main rock-forming and liquidus minerals of Phase II. Saturation in remaining bulk melt with components needed for nucleation of EGM was reached after the crystallization about 85 vol. % of the intrusion. Early euhedral and idiomorphic EGM of Phase III crystalized in a large convective volume of melt together with other liquidus minerals and was affected by layering processes and formation of EGM ore. Consequently, a prerequisite for the formation of the ore deposit is saturation of the alkaline bulk magma with EGM. It follows that the potential for EGM ores in Lovozero is restricted to the parts of the complex that hosts cumulus EGM. Phase II with only anhedral and interstitial EGM is not promising for this type of ore. -
Li in Minerals from the Ilimaussaq Alkaline Intrusion, South Greenland
Li in minerals from the Ilimaussaq alkaline intrusion, South Greenland J. C. BAILEY, H. BOHSE, R. GWOZDZ and J. ROSE-HANSEN Bailey, J.C., Bohse, H., Gwozdz, R. and Rose-Hansen, J. 1993. Li in minerals from the Ilfmaussaq alkaline intrusion, South Greenland. Bulletin of the Geological Society of Denmark, vol. 40, pp. 288-299. Copenhagen 1993-12-30. https://doi.org/10.37570/bgsd-1993-40-13 Li was analysed by instrumental neutron activation analysis and Cerenkov counting in 120 mineral samples (30 species) from the Ilfmaussaq alkaline intrusion, South Greenland. More than 0.23 wt.% Li (0.5 wt.% Li2O) is found in polylithionite, neptunite, riebeckite, Na-cookeite, ephesite, arfvedsonite, gerasimovskite and astro phyllite. Arfvedsonite (200-2500 ppm Li) carries the bulk of Li in most of the highly alkaline rocks. Li-Mg and Li-F relations indicate that the distribution of Li is con trolled by the structure of minerals, their absolute contents of Mg and F and the fractionation stage within the intrusion. Li is probably linked with Fin the fluid state and this linkage continues into crystallising phases where Li occupies sites which also accommodate Mg. Li/Mg and Li/F ratios of Ilfmaussaq rocks and minerals are higher than in equivalent materials from the Lovozero intrusion (Kola, Russia). The Li Mg-Fe2+ geochemical association at Ilfmaussaq (Fe2+>>Mg) and Lovozero (Fe2+>Mg) contrasts with the commercially important Li-rich but Mg-Fe2+-poor association found in certain granite pegmatites and greisenised granites. Bailey, J. C., Bohse, H., Gwozdz, R. & Rose-Hansen,- J. Division for Petrology, Geological Institute, v)ster Voldgade 10, DK-1350 Copenhagen K, Denmark. -
New Minerals Approved Bythe Ima Commission on New
NEW MINERALS APPROVED BY THE IMA COMMISSION ON NEW MINERALS AND MINERAL NAMES ALLABOGDANITE, (Fe,Ni)l Allabogdanite, a mineral dimorphous with barringerite, was discovered in the Onello iron meteorite (Ni-rich ataxite) found in 1997 in the alluvium of the Bol'shoy Dolguchan River, a tributary of the Onello River, Aldan River basin, South Yakutia (Republic of Sakha- Yakutia), Russia. The mineral occurs as light straw-yellow, with strong metallic luster, lamellar crystals up to 0.0 I x 0.1 x 0.4 rnrn, typically twinned, in plessite. Associated minerals are nickel phosphide, schreibersite, awaruite and graphite (Britvin e.a., 2002b). Name: in honour of Alia Nikolaevna BOG DAN OVA (1947-2004), Russian crys- tallographer, for her contribution to the study of new minerals; Geological Institute of Kola Science Center of Russian Academy of Sciences, Apatity. fMA No.: 2000-038. TS: PU 1/18632. ALLOCHALCOSELITE, Cu+Cu~+PbOZ(Se03)P5 Allochalcoselite was found in the fumarole products of the Second cinder cone, Northern Breakthrought of the Tolbachik Main Fracture Eruption (1975-1976), Tolbachik Volcano, Kamchatka, Russia. It occurs as transparent dark brown pris- matic crystals up to 0.1 mm long. Associated minerals are cotunnite, sofiite, ilin- skite, georgbokiite and burn site (Vergasova e.a., 2005). Name: for the chemical composition: presence of selenium and different oxidation states of copper, from the Greek aA.Ao~(different) and xaAxo~ (copper). fMA No.: 2004-025. TS: no reliable information. ALSAKHAROVITE-Zn, NaSrKZn(Ti,Nb)JSi401ZJz(0,OH)4·7HzO photo 1 Labuntsovite group Alsakharovite-Zn was discovered in the Pegmatite #45, Lepkhe-Nel'm MI. -
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. -
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. -
Okanoganite, a New Rare-Earth Borofluorosilicate from the Golden Hom Batholitb Okanogancounty, Washington
American Mineralogist, Volume 65, pages II38-1142, 1980 Okanoganite, a new rare-earth borofluorosilicate from the Golden Hom batholitb OkanoganCounty, Washington Russnrr C. Boccs Departmentof GeologicalSciences, University of Califurnia Santa Barbara, Califurnia 93106 Abstract Okanoganite is found in miarolitic cavities in the arfvedsonite granite phase of the Golden Horn batholith, near Washington Pass,Okanogan County, $y'ashington.It occurs as tan to pale pink pseudotetrahedraltwinned crystalsup to 4 mm across.A combination of electron microprobe analysesand spectrophotometric analyses for B2O3give the following formula: (Nau*Car.*Pboro)[(Y,Ce,Nd,La)rr".rCar.^Fe,u,](Si,r rrTlo*)Bu*Or, -F42.4r,with an ideal for- mula of (Na,Ca)r(Y,Ce,Nd,La),rSi5B2O27FA.The crystals are pseudotetrahedralfourlings with twin plane {0114}, the c face of each individual forming the faces of the pseudo- tetrahedron. The mineral is rhombohedral with possible spacegroup R3, R3, R32,R3m, R3m, R3c,or R3c.The cell dimensionsare 4 : 10.12(l),c : 27.05(8)A,Z:3 (hexagonalcell) or a :10.94(3)A,a:58.?(3)",2:l(rhombohedralcell).D(meas):4.35,D(calc):4.37.Ttie strongestlines [4 I), (hkl)l of the X-ray powder pauern (68 given) are 4.38(4\QA); 3.rr(a8)(300); 2.e70(100X027); 2.e3e(e5)(125); 2.e26(s0)(303); 2.676(32)(220); 1.978(35X325,413);1.822(32)(3.0.12); 1.784(43X330,2.0.14). The refractive indices are a : 1.753,e: 1.740;the mineral showsno dichroism and is colorlessin thin fragments;streak : white; H : 4. -
Agpaitic and Miaskitic Nepheline Syenites of The
Canadian Minelalogist Vol. 28, pp.25l-266 (1990) AGPAITIC AND MIASKITIC NEPHELINESYENITES OF THE MCGERRIGLEPLUTONIC COMPLEX. GASPE, OUEBEG: AN UNUSUAL PETROLOGICALASSOCIATION* GRAEME M. WALLACE Depaftmentof GeologicalSciences, McGill University,3450 UniversityStreet, Montreal, QuebecH3A 2A7 JOSEPH B. WHALEN GeologicalSumey of Canado,601 Booth Strcet, Ottawa,Ontario KIA 0E8 ROBERT F. MARTIN Department of Geological Sciencesand Mineral Exploration ResearchInstitute, McGill University, 3450 UniversityStreet, Montreal, QuebecH3A 2A7 ABSTRAcT dansun r€servoircrustal pourrait avoir fourni le flux de chaleurrequis pour une fusion partielle du protolithedes The dominantly granitic Early Devonian McGerrigle plu- rochesgranitiques. Cette hypothbse explique Ia miseen place tonic complex, in the Gasp6region of Quebec,contains demagmas contemporains sous-satur6 et sursaturden silice minor volumesof 1) miaskitic and 2) sodalite- aenigma- dansle massifde McGerrigle. Ce sch6ma requiert une cham- tite - astrophyllite - arfvedsonite-bearingagpaitic nephe- bre magmatiquetrCs stable, donc un milieu en extension line syenites. Significant mineralogical variations in these le long d'un rift ou d'unefaille transformante. rocks principally reflect the aepaitic index andflO) of the magma,These geochemically highly evolvedundersaturated Mots-clds:sy6nite n6ph6linique, miaskitique, agpaitique, rocks probably representthe products of fractionation of granite,contamination crustale, complexe de McGer- mildly alkaline mafic magma(s). Isotopic data imply that rigle,Gaspdsie, Qu€bec. batchesof juvenile syenitic magma were variably contami- nated by minor volumes of crustal material. Fractionation of mafic magmasin a crustal reservoir could have supplied INTRODUCTION heat to partially melt the protolith of the granitic rocks. This proposal accounts for the contemporaneoussupply The nephelinesyenites of the generallygranitic of silica-undersaturatedand silica-oversaturatedrock-types McGerrigle plutonic complex, Gasp6 Peninsula, in the McGerrigleplutonic complex.Our proposalis con- (Fig. -
The House Composers of the Theater Auf Der Wieden in the Time of Mozart (1789-91)1
The House Composers of the Theater auf der Wieden in the Time of Mozart (1789-91)1 DAVID J. BUCH Some of the most important theatrical music in Europe was produced at the Theater auf der Wieden in suburban Vienna in the years 1789 to 1801. Beginning with the immensely popular Die zween Anton oder der dumme Gärtner aus dem Gebirge in July 1789, Emanuel Schikaneder produced one successful singspiel after another. The most successful of these were quickly staged in other European venues, both in the original German and in translation.2 Yet, until recently, we have known only a single opera from that period, Mozart’s Die Zauberflöte. Because scholars have not studied this repertory,3 a myth of singularity for Mozart’s singspiel has dominated the secondary literature. But Mozart’s opera was in fact the fourth in a series of fairy-tale singspiels based on texts associated with Christoph Martin Wieland. And the music of Mozart’s singspiel is firmly rooted in a unique style developed at the theater by a group of talented composers who interacted with Mozart, both learning from the master and influencing him in turn. Another myth about this theater has also persisted in modern literature, namely, that the music was of an inferior quality and that the performances were rather crude. While there is one derisive review of a performance at the Theater auf der Wieden by a north German commentator in 1793,4 most contemporary reviews were positive, noting a high standard of musical performance. In his unpublished autobiography, Ignaz von Seyfried recalled performances of operas in the early 1790s by Mozart, Süßmayr, Hoffmeister etc., writing that they were performed with rare skill (ungemein artig). -
Download the Scanned
American Mineralogist, Volume 78, pages1314-1319, 1993 NEW MINERAL NAMES* JonN L. Jlnrnon Department of Earth Sciences,University of Waterloo, Waterloo, Ontario N2L 3G1, Canada Dlvro A. VaNxo Department of Geology, Georgia State University, Atlanta, Georyia 30303, U.S.A. Bearthite* Cancrisilite* C. Chopin, F. Brunet, W. Gebert, O. Medenbach,E. Till- A.P. Khomyakov, E.I. Semenov, E.A. Pobedimskaya, manns(1993) Bearthite, CarAl[POo]r(OH), a new min- T.N. Nadezhina, R.K. Rastsvetaeva(1991) Cancrisilite eral from high-pressureterranes of the western Alps. Nar[AlrSirOro]COr.3HrO:A new mineral of the can- Schweiz.Mineral. Petrogr. Mitt., 73, l-9. crinite group. Zapiski Vses. Mineral. Obshch., 120(6), 80-84 (in Russian). Electron microprobe analysesof the holotype sample from the Monte Rosa massif, Z,ermatt Valley, Switzer- The reportedchemical composition is NarO 21.30,KrO land, gave CaO 33.04, SrO 3.53, MgO 0.12, FeO 0.03, 0.10,CaO 0.68, MnO 0.1l, FerO.0.33,AlrO3 24.42,5iO, AlrO3 15.91,CerO, 0.04, LarO30.03, SiO, 0.30, PrO, 43.11,CO2 4.82, SO3 0.36, HrO 5.01,sum 100.24wto/o, 44.32, SO30.01, F 0.48, Cl 0.02, sum (lessO = F, Cl) correspondingto (Nau.rIQorCao ,rFeo ooMgo or)"r ro(Alo,*o- 97.62wto/o, corresponding to (Ca3,oSro ,r)r, nu(Al, ,r- Si, 2o)",2ooo2o ,o(COr), r0(SOo)0 0o'2.79HrO, ideally NarAlr- Mgoor)"r 00(P3 eTsio 03)>o ooFo ,u, closeto the ideal formula SirOr4CO3.3HrO.Dissolves readily with effervescenceat CarAl[POo]r(OH), with OH confirmed by structural re- room temperature in l0o/oHCl, HNO3, and HrSOo. -
Leaching of Rare Earths from Eudialyte Minerals
Western Australia School of Mines Leaching of Rare Earths from Eudialyte Minerals Hazel Lim This thesis is presented for the Degree of Doctor of Philosophy of Curtin University June 2019 Abstract Rare earths are critical materials which are valued for their use in advanced and green technology applications. There is currently a preferential demand for heavy rare earths, owing to their significant applications in technological devices. At present, there is a global thrust for supply diversification to reduce dependence on China, the dominant world supplier of these elements. Eudialyte is a minor mineral of zirconium, but it is currently gaining significance as an alternative source of rare earths due to its high content of heavy rare earths. Eudialyte is a complex polymetallic silicate mineral which exists in many chemical and structural variants. These variants can also be texturally classified as large or fine-grained. Huge economic deposits of eudialyte can be found in Russia, Greenland, Canada and Australia. Large-grained eudialyte mineralisations are more common than its counterpart. The conventional method of eudialyte leaching is to use sulfuric acid. In few instances, rare earths are recovered as by-products after the preferential extraction of zirconium . As such, the conditions for the optimal leaching of rare earths, particularly of heavy rare earths from large-grained eudialyte are not known. Also, previous studies on eudialyte leaching were focused only on large-grained eudialyte and thus, there are no known studies on the sulfuric acid leaching of rare earths from finely textured eudialyte. Additionally, the sulfuric acid leaching of eudialyte bears a cost disadvantage owing to the large volume of chemicals needed for leaching and for neutralising effluent acidity on disposal.