Petrological Implication of Wagnerite-Ma5bc in the Quartzofeldspathic Gneiss, Larsemann Hills, East Antarctica*

Total Page:16

File Type:pdf, Size:1020Kb

Petrological Implication of Wagnerite-Ma5bc in the Quartzofeldspathic Gneiss, Larsemann Hills, East Antarctica* PROGRESS IN NATURAL SCIENCE V ol .15 , No .6 , June 2005 Petrological implication of wagnerite-Ma5bc in the quartzofeldspathic gneiss, Larsemann Hills, East Antarctica* REN Liudong 1** , Edw ard S .GREW2 , XIONG M ing3 and WANG Yanbin1 (1 .Institute of Geology , C hinese Academy of Geological S ciences, Beijing 100037 , China;2.Departmen t of Earth Sciences, University of M aine, 5790 Edw ard T .Bryand Research Center , Orono , Maine 04469-5790 , USA;3 .China University of Geosciences, Beijing 100083 , China) Received September 23 , 2004 ;revised October 21 , 2004 Abstract Wagnerite-Ma5bc polytype is found in a gneiss associated with cordierite-prismatine-bearing gneiss, northern Stornes Peninsula, Larsemann Hills, East Antarctica.Wagnerite coexists with apatite and both of them are presen t as rock-forming minerals.Ca depletion is not essential to the formation of w agnerite;sufficient Mg , P and F components, and a relatively low Ca/ Mg ratio is critical, otherwise only apatite crystallizes.S trong anatexis of the quartzofeldspathic gneiss of the area results in differentiation and separate en rich- ment of leuco- and m elanocratic components.P and F tend to accumulate in the mafic-rich melanocratic componen t, and w hen their abun- dance reaches certain concentration , w agnerite forms.It is perhaps the chemistry of the setting that con trols the appearance of wagnerite , w hereas the PT condition is responsible for the variety of w agnerite polytype.A disordered polytype crystallizes at relatively high tempera- ture, then cools dow n slow ly and transforms into one of the ordered polytypes, in this case, the Ma5 bc polytype. Keywords: wagnerite-Ma5 bc polytype, anatexis, formation condition, volatile components, Larsemann Hills. M g-dominant minerals of w ag nerite-triplite assemblage in the study area . g roup, i .e .(Mg , Fe , M n)2 (PO 4)(F , OH), are relatively rare , but have been found in a wide variety 1 Regional geology of geologic environments, including metamorphic rocks of all g rades[ 1] such as quartz-carbonate veins of The Larsemann Hills were once situated at the hydrothermal origin , pegmatites , kyanite-quartzite , East Antarctic craton of the Gondwana superconti- mica schist , sillimanite gneiss , and magnetite ores . nent , w here the c .550 M a Pan-African tectonother- mal event w as intensively developed[ 9] .A suite of Up to now , w agnerite is present mainly as the high amphibolite-g ranulite facies rocks is present in Ma2bc poly type , an accessory mineral in calcium- this region , and among them the sillimanite-garnet poo r rocks[ 2 , 5] in w hich apatite , if present , often oc- gneisses , and the quartzofeldspathic gneisses are the curs as retrog rade rim around wagnerite .Henriques[ 6] main types , w hich are intercalated w ith pyroxene-bi- reported a small amount of w ag nerite and apatite in otite-plagioclase g neiss , biotite-plagioclase gneiss, mi- kyanite-quartzite , but the relation between the two nor granitic g neiss , hornblende-tw o pyroxene g ran- minerals w as not mentioned .The wagnerite-bearing ulite , and calc-silicates .In addition , some g ranites rocks generally have o ther phosphate minerals like and pegm atites are also present . monazite and xeno time . The gneiss containing w agnerite-Ma5bc occurs The poly type with a 5-fold b-dimension repeat in the core of w hat appears to be a fold in banded w as first discovered on Sto rnes Peninsula in the cordierite-prismatine gneiss (Fig .1).Prismatine and Larsemann Hills , East Antarctica[ 7, 8] .The Larse- cordierite also form coarse-g rained segregations and mann Hills rock is distinctive in that wagnerite coex- nodules associated w ith quartzofeldspathic seg rega- ists with apatite and bo th are present as major rock- tions . Given the presence of Al-rich minerals forming constituents , w hich has not been reported cordierite and prismatine , the gneisses illustrated in befo re .This paper focuses on the petrolog ical implica- Fig .1 most likely have sedimentary precursors that tions and geological setting of the w agnerite-apatite were subsequently modified by migm atization . *S upported by the National Natural Science Foundation of China (Grant No.40172065 ), the Chinese Geological Survey (Grant No . 200413000023)and Programme of Excellent Young Scientists of the Ministry of Land and Resources ** To w hom correspondence should be addressed .E-mail:ldren @cags.net .cn 524 w ww .tandf.co .uk/journals Prog ress in Natural Science Vol .15 No .6 2005 The g neiss lacks obvious foliation .Majo r con- cracks and g rain boundaries of w ag nerite-Ma5bc stituents are plagioclase , w ag nerite-Ma5bc , apatite (Fig .1).Sy mplectitic intergrow ths of cordierite and m agnetite ; subordinate are biotite , quartz , w ith K-feldspar were developed (Fig .2), w hich may potassium feldspar , cordierite , minerals of the mon- correspond to the sapphirine-orthopy roxene symplec- azite and xenotime g roups , co rundum , lamellar tite after w ag nerite in Eastern Ghats Land , India[ 14] . hem atite-ilmenite interg row ths , hercynite , and sul- In sum mary , tex tures are consistent w ith a primary fide . assemblage :wagnerite-Ma5bc + plagioclase + ap- atite(1) + mag netite + ilmenite-hem atite . The conditions for the metamorphic peak gran- ulite facies in the Larsem ann Hills are 750 to -860 ℃ at 0 .6 —0 .7 GPa[ 10 —13] . Fig .2 . BSE image of Kfs-Crd symplectite after wagnerite (the background is Kfs). Although interlayered w ith cordierite-prismatine gneiss, the w ag-bearing gneiss has no t the contact Fig.1 . BS E image of Wag-Ap and late Kfs and Ap2. tex ture betw een w ag and prs .By combining the rela- tively earlier crystallization of wag than monazite- 2 Petrography and texture feature xenotime in the g neiss w hile in the prs g neiss mnz- x nt formed earlier , the possible mineral cry stallization Generally situated between mineral g rains such sequence relative to wag can be summarized as follow s [ 28] as plagioclase , wagnerite has a straight contact with (mineral abbreviations are after Kretz ): apatite (Fig .1), w hich suggests the essentially co- Bt , Pl※Mt -Ap1 +Wag +Mnz +Xnt +Ilm existing feature of the tw o minerals .Wag nerite local- -Hem +Crn ※Prs※Kfs , ly occupying the position of apatite implies the earlier Crd -Kfs ;Ap2 ※pinite . beginning of apatite and late finishing of w ag nerite . Predating prism atine and the crd-kfs sy mplectite , the Following apatite and w agnerite are monazite and fo rmation of w agnerite is related to the biotite dehy- xenotime in small amount , and betw een them are ba- dration reactio n w ith plag ioclase involved in anatexis, sically co-existing relationships .Meanw hile , opaque and should be the stage of g arnet in quartzofeldspathic minerals like m agnetite , ilmenite and hematite are gneisses , that is, wagnerite formed at the peak meta- formed , and their volume in the rock can reach 15 %. morphism . Wagnerite-Ma5bc forms anhedral to euhedral Semi-quantitative energy spectrum com position g rains mostly 0 .5 —2 mm across (the maximum is scanning demonstrates that from Ap1 to Ap2 , Mg and about 2 .5 mm).Some g rains have a tabular habit and P tend to increase , w hile Na , Ca , Fe , and S tend to the thickness can be less than 0 .1 mm ;a few of them decrease . show two terminal faces .Wagnerite-Ma5bc is com- 3 Crystal structure of wagnerite monly dusty with fine inclusions o r discolored by in- cipient alteration .Textures suggest two generations By using a Bruker Smart Apex CCD sy stem and of apatite :relatively coarse grains with alig ned acicu- g raphite-monochrom ated Mo Kαradiation , the crystal lar inclusions ; rare margins fring ing w agnerite- structure of w agnerite is measured and the unit-cell Ma5bc (Fig .1)or overgrow ths separating w ag ner- parameters w ere obtained by least-squares refine- ite-Ma5bc from oxide and sulfide inclusions .Micro- ment , a =9 .645(2) , b =31 .659(6) , c = scopic seams of apatite have also developed along 11 .914(2) , β =108 .26 (3)°, V =3455(1) 3 , Prog ress in Natural Science Vol.15 No .6 2005 w ww .tandf.co .uk/journals 525 and Z =40 .The wagnerite-Ma5bc[ 7 , 8] , space group 4 Mineral chemistry Ia , distinct to that of the type w ag nerite , 2b poly- type (space g roup P 2/ a), is a new poly type .The Microprobe analyses of w ag nerite are given in prim ary difference betw een the w ag nerite-Ma5bc and Table 1 .Assuming Fe , Ti , Ca , and M n substitute w agnerite-Ma2bc is ordering of the (F , OH)posi- fo r M g , all the spots(except spots 1-1 and 3-1) tions.F can occupy one of the two positions , w hich give the average composition as follows :(Mg19.050 can result in tw o distinct configurations along the a Fe1.006Ti0.192Ca0 .030 Mn0.023)20.301(P9.982Si0.018)10.000 direction .Other polyty pes have been summarized by O40 F6 .485 (OH )3 .545 ;the presence of hydroxy l was Chopin et al .[ 15] . confirmed by Raman spectroscopy . Table 1 . Microprobe analyses of w agneritea) Oxides 1-1 1-2 2-2 2-3 2-5 2-6 2-7 3-1 3-2 3-3 4-1 8-4 8-2 MgO 43.59 44 .13 44 .99 45 .15 44 .29 45 .05 45 .07 42 .59 44 .45 43 .85 44 .80 44 .85 45 .03 SiO 2 0.064 0 .056 0 .061 0 .077 0 .053 0 .027 0 .080 0 .051 0 .057 0 .053 0 .084 0 .072 0 .075 CaO 0.088 0 .105 0 .081 0 .084 0 .071 0 .075 0 .080 2 .374 0 .089 0 .097 0 .084 0 .129 0 .158 TiO 2 0.974 0 .954 0 .851 0 .826 0 .821 0 .745 0 .722 0 .975 1 .028 0 .949 0 .974 1 .007 0 .924 MnO 0.084 0 .096 0 .088 0 .058 0 .095 0 .078 0 .106 0 .089 0 .132 0 .121 0 .065 0 .088 0 .12 FeO 4.153 4 .809 4 .236 4 .100 4 .610 2 .563 4
Recommended publications
  • Mineralogy and Geology of the \Vkgnerite Occurrence Co Santa Fe Mountain, Front Range, Cobrado
    Mineralogy and Geology of the \Vkgnerite Occurrence co Santa Fe Mountain, Front Range, Cobrado GEOLOGICAL SURVEY PROFESSIONAL PAPER 955 Mineralogy and Geology of the Wignerite Occurance on Santa Fe Mountain, Front Range, Colorado By DOUGLAS M. SHERIDAN, SHERMAN P. MARSH, MARY E. MROSE, and RICHARD B. TAYLOR GEOLOGICAL SURVEY PROFESSIONAL PAPER 955 A detailed mineralogic study of wagnerite, a rare phosphate mineral occurring in the report area in Precambrian gneiss; this is the first recorded occurrence of wagnerite in the United States UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1976 UNITED STATES DEPARTMENT OF THE INTERIOR THOMAS S. KLEPPE, Secretary GEOLOGICAL SURVEY V. E. McKelvey, Director Library of Congress Cataloging in Publication Data Main entry under title: Mineralogy and geology of the wagnerite occurrence on Santa Fe Mountain, Front Range, Colorado. (Geological Survey Professional Paper 955) Includes bibliographical references. 1. Wagnerite Colorado Santa Fe Mountain. 2. Geology Colorado Santa Fe Mountain. I. Sheridan, Douglas M., 1921- II. Series: United States Geological Survey Professional Paper 955. QE391.W3M56 549'.72 76-10335 For sale by the Superintendent of Documents, U.S. Government Printing Office Washington, B.C. 20402 Stock Number 024-001-02844-1 CONTENTS Page Metric-English equivalents .............................. Descriptive mineralogy Continued Page Abstract............................................................ 1 Wagnerite............................................... 5 Introduction....................................................
    [Show full text]
  • Phosphates, Arsenates, Vanadates, Antimonates A
    592 DESCRIPTIVE MINERALOGY Epistdite. A niobate of uncertain composition. Analysis shows chiefly SjOz, TiOz, NkO, H20. Monoclinic. In rectangular plates, also in aggregates of curved foha. Basal cleavage perfect. H. = 1-1.5. G. = 2.9. Color white, grayish brownish. Refractive index 1.67. Bound in pegmatite veins or in massive albite from ~llianehaab,Greenland. Plumboniobite. A niobatc of yttrium, uranium, lead, iron, etc. Amorphous. H. = 5-5'5. G. = 4.81. Color dark brown to black. Found in mica mines at Morogoro, German Enst Africa. Oxygen Salts 4. PHOSPHATES, ARSENATES, VANADATES, ANTIMONATES A. Anhydrous Phosphates, Arsenates, Vanadates, Antimonates Normal phosphoric acid is H3P04, and consequently normal phosphates I 11 m have the formulas RtPOa, R3(PO4)2 and RPO4, and similarly for the arse- nates, etc. Only a comparatively small number of species conform to this simple formula. Most species contain more than one metallic element, and in the prominent Apatite Group the radical (CaF), (CaCI) or (PbCI) enters; " in the Wagnerite Group we have similarly (kF) or (ROH). XENOTIME. Tetragonal. Axis c = 0.6187, zz' (1 11 A ill) = 55" 301, 22" (111 A 771) = 82" 22'. In crystals resembling zircon in habit; sometimes compounded with zircon in parallel position (Fig. 462, p. 173). In 972 rolled grains. Cleavage: m (110) perfect. Fracture uneven and splintery. Brittle. H. = 4-5. G. = 4.454.56. Luster resinous to vitreous. Color yellowish brown, reddish brown, hair-brown, flesh-red, grayish white, wine-yellow, pale yellow; streak pale brown, yellow- ish or reddish. Opaque. Optically + . w = 1.72. e = 1-81.
    [Show full text]
  • Sintering and Mechanical Properties of Magnesium and Fluorine Co-Substituted Hydroxyapatites
    Journal of Biomaterials and Nanobiotechnology, 2013, 4, 1-11 1 http://dx.doi.org/10.4236/jbnb.2013.41001 Published Online January 2013 (http://www.scirp.org/journal/jbnb) Sintering and Mechanical Properties of Magnesium and Fluorine Co-Substituted Hydroxyapatites Samia Nsar, Amel Hassine, Khaled Bouzouita* Laboratory of Industrial Chemistry, National School of Engineering, Sfax, Tunisia. Email: *[email protected] Received September 5th, 2012; revised October 17th, 2012; accepted November 10th, 2012 ABSTRACT Biological apatites contain several elements as traces. In this work, magnesium and fluorine co-substituted hydroxyapa- tites with the general formula Ca9Mg(PO4)6(OH)2-yFy, where y = 0, 0.5, 1, 1.5 and 2 were synthesized by the hydrother- mal method. After calcination at 500˚C, the samples were pressureless sintered between 950˚C and 1250˚C. The substi- tution of F− for OH− had a strong influence on the densification behavior and mechanical properties of the materials. Below 1200˚C, the density steeply decreased for y = 0.5 sample. XRD analysis revealed that compared to hydroxyl- fluorapatite containing no magnesium, the substituted hydroxyfluorapatites decomposed, and the nature of the decom- position products is tightly dependent on the fluorine content. The hardness, elastic modulus and fracture toughness of these materials were investigated by Vickers’s hardness testing. The highest values were 622 ± 4 GPa, 181 ± 1 GPa and 1.85 ± 0.06 MPa·m1/2, respectively. Keywords: Hydroxyapatite; Magnesium, Fluorine; Sintering; Mechanical Properties 1. Introduction tite containing magnesium and fluorine would be more suitable for dental and orthopedic applications. Hydroxyapatite (HA) is widely used in orthopedic and Hence, it is thought worthwhile to synthesize and char- reconstructive surgery thanks to its excellent bioactivity acterize Mg/F-co-substituted hydroxypatites.
    [Show full text]
  • Thermal Characterization of Magnesium Containing Ionomer Glasses
    Thermal characterization of magnesium containing ionomer glasses ELENI MARIA KARTELIA Supervisor: Dr. A. Stamboulis Thesis submitted for the degree of MRes Biomaterials University of Birmingham School of Engineering Department of Metallurgy and Materials September, 2010 University of Birmingham Research Archive e-theses repository This unpublished thesis/dissertation is copyright of the author and/or third parties. The intellectual property rights of the author or third parties in respect of this work are as defined by The Copyright Designs and Patents Act 1988 or as modified by any successor legislation. Any use made of information contained in this thesis/dissertation must be in accordance with that legislation and must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the permission of the copyright holder. ACKNOWLEDGMENTS I would like to thank my supervisor Dr. A. Stamboulis for her help and encouragement during my project. Without her support, I feel that I would not have been able to complete this work. I would also like to express my gratitude to Dr. D. Holland at University of Warwick for her helping on DSC measurements. Many thanks are given to academic staff and technicians of the School of Metallurgy and Materials. I would like to thank sincerely the Phd students Praveen Ramakrishnan, Georgina Kaklamani, Siqi Zhang and Mitra Kashani for their significant help through my experimental work. Last but not least, I would like to thank my family for their support and understanding. Special thanks to Thanos Papaioannou. 2 TABLE CAPTIONS CHAPTER 2: MATERIALS AND METHODS Table 2.1.2: Composition of Mg substituted alumino-silicate glasses.
    [Show full text]
  • The Crystal Structure of Althausite, Mg.(P04)2(OH,O)(F,D)
    ----- ----- American Mineralogist, Volume 65, pages 488-498, 1980 The crystal structure of althausite, Mg.(P04)2(OH,O)(F,D) CHRISTIAN R0MMING Kjemisk Institutt, Universitetet i Oslo, Blindern, Oslo 3, Norway AND GUNNAR RAADE Instituttfor Geologi, Universitetet i Oslo, Blindern, Oslo 3, Norway Abstract The crystal structure of althausite was solved by direct methods and refined to a final R value of 0.022 for 1164 high-angle reflections (sin 8/A > 0.45A -I) with I> 2.50. The position of the hydrogen atom was found from a difference Fourier synthesis. The structure is ortho- rhombic Pnma with a = 8.258(2),b = 6.054(2),c = 14.383(5)A.Magnesium atoms occur in both five- and six-fold coordination, and the coordination polyhedra are highly distorted. The Mg octahedra form chains along b by edge-sharing. Hydroxyl and fluorine occur in a largely ordered distribution among two different structural sites and occupy alternating posi- tions along 'channels' parallel to b. Partial vacancy in the (OH,F) sites is confirmed, the pop- ulation factor for the F site being 81 percent. The crystal-chemical formula of althausite is therefore Mg4(P04)2(OH,0)(F,D) with Z = 4. The cleavages in althausite, {001} perfect and {101} distinct, occur along planes crossing relatively few bonds and leave the chains of Mg octahedra unbroken. Bond-strength calcu- lations for althausite and wagnerite are presented and the OH content in wagnerite is dis- cussed. Preliminary results of hydrothermal syntheses indicate the existence of a series from F- wagnerite to OH,F-wagnerite and from OH-althausite to OH,F-althausite.
    [Show full text]
  • Synthetic Phase with the Structure of Apatite
    Chapter 4 Synthetic Phase with the Structure of Apatite Petr Ptáček Additional information is available at the end of the chapter http://dx.doi.org/10.5772/62212 Abstract The previous chapters were dedicated to description of structure and properties of minerals from supergroup of apatite and introduction of method for identification and investigation of properties of phosphate minerals. The first synthesis of apatite was performed by Daubrée by passing the PCl3 vapor over red-hot lime. The fourth chapter of this book introduces techniques for the preparation of synthetic analogs of apatite minerals including solid-state synthesis, wet chemical methods, hydrothermal synthesis as well as methods for preparation of single crystals. Chapter continues with descrip‐ tion of structure and properties of synthetic compounds of apatite type and ends with incorporation of 3d-metal ions into the hexagonal channel of apatite. Keywords: Apatite, Solid-State Synthesis, Wet Chemical Methods, Hydrothermal Synthesis, Single crystal, Lacunar Apatite The first synthesis of apatite was performed by DAUBRÉE [1], who obtained it in crystals by passing the vapor of phosphorus trichloride (PCl3) over red-hot lime. The synthetic mineral analogues of chlorapatite, fluorapatite, or the mixtures of these phases were prepared by MANROSS [2] via fusing of sodium phosphate either with calcium chloride, calcium fluoride, or both together. The similar process was also successfully used by BRIEGLEB [3]. FORCHHAMMER [4] prepared chlorapatite by fusing calcium phosphate with sodium chloride. When bone ash or marl was used instead of artificial calcium phosphate, mixed apatite was formed. Similar results were reported by DEVILLE and CARON [5], who fused bone ash with ammonium chloride and either calcium chloride or fluoride, and also by DITTE [6], who repeated Forchhammer’s © 2016 The Author(s).
    [Show full text]
  • The Crystal Structure of Althausite, Mg.(Poj2(OH,O)(F,D)
    American Mineralogist, Volume 65, pages 4gg_49g, Igg0 The crystal structure of althausite,Mg.(pOJ2(OH,O)(F,D) CunIsrnN RoutvilNc Kjemisk Institutt, (Jniyersiteteti Oslo, Blindern, Oslo 3, Norway AND GUNNEN RAEOS Instituttfor Geologi, (lniversitetet i Oslo, Blindern, Oslo 3, Norway Abstract The crystal structure of althausitewas solved by direct methods and refined to a final R valueof 0'022for l164 high-anglereflections (sin d/I > 0.45A-r)with 1> 2.5o.Theposition of the hydrogenatom was found from a differenceFourier synthesis.The structureis ortho- : rhombic Pnma with a 8.258(2),b : 6.05aQ),c : 14.383(5)A.Magnesium atoms occur in both five- and six-fold coordination, and the coordination polyhedia are highly distorted. The Mg octahedraform chains along D by edge-sharing.Hydroxyl anA fluoine occur in a largely ordereddistribution among two diflerent structural siies 'channels'parallel and occupy alternatingposi- tions along to D.Partial vacancyin the (OH,F) sitesis dnfirmed, the pop- ulation factor for the F site being 8l percent.The crystal-chemicalformula of althausiteis thereforeMgo@Oo)r(OH,OXF,!) with Z: 4. The cleavagesin althausite, {00U perfect and {l0l} distinct, occur along planes crossing relatively few bonds and leave the chains of Mg octahedraunbroken. Bond-strengthcalcu- lations for althausiteand wagnerite are presentedand the OH content in wagner-iteis dis- cussed. Preliminary results of hydrothermal synthesesindicate the existenceof a seriesfrom F- wagneriteto OH,F-wagneriteand from OH-althausiteto OH,F-althausite.Infrared spectraof fluorine-free althausiteshow a splitting of the O-H stretchingfrequency, proving ih"t t*o distinct hydroxyl positionsare present. Introduction agreement with the calculated value, (010) n (l l0) : 60.14".
    [Show full text]
  • Mineralogic Notes Series 3
    DEPARTMENT OF THE INTERIOR FRANKLIN K. LANE, Secretary UNITED STATES GEOLOGICAL SURVEY . GEORGE OTIS SMITH, Director Bulletin 610 MINERALOGIC NOTES SERIES 3 BY WALDEMAR T. SCHALLER WASHINGTON GOVERNMENT PRINTING OFFICE 1916 CONTENTS. Page. Introduction................................................................ 9 Koechlinite (bismuth molybdate), a new mineral............................ 10 Origin of investigation................................................... 10 Nomenclature......................................................... 10 Locality............................................................... 11 Paragenesis........................................................... 11 Crystallography........'............................................... 14 General character of crystals....................................... 14 Calculation of elements............................................. 14 Forms and angles................................................. 15 Combinations..................................................... 19 < Zonal relations and markings...................................... 19 Habits........................................................... 21 Twinning........................................................ 23 Measured crystals................................................. 26 Etch figures...................................................... 27o Intergrowths........................................................ 31 Relation to other minerals.......................................... 31 Physical properties...................................................
    [Show full text]
  • Lazulite Mgal2(PO4)2(OH)2 C 2001-2005 Mineral Data Publishing, Version 1 Crystal Data: Monoclinic
    Lazulite MgAl2(PO4)2(OH)2 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. As crystals, stubby to acute dipyramidal with forms {111}, {111}, {101}, to 15 cm, or tabular on {111} or {101}, with several other forms noted; granular, massive. Twinning: Common on {100} with composition plane {001} and marked re-entrant, occasionally producing lamellar or polysynthetic groups; rare on {223};by reflection on {221} with composition plane {331}; several other twin laws reported. Physical Properties: Cleavage: Poor to good on {110}; indistinct on {101}. Fracture: Uneven to splintery. Tenacity: Brittle. Hardness = 5.5–6 D(meas.) = 3.122–3.240 D(calc.) = 3.144 Optical Properties: Transparent to translucent, may be nearly opaque. Color: Azure-blue, sky-blue, bluish white, yellow-green, blue-green, rarely green. Streak: White. Luster: Vitreous. Optical Class: Biaxial (–). Pleochroism: Strong; X = colorless; Y = blue; Z = darker blue. Orientation: Y = b; X ∧ c =10◦. Dispersion: r< v,weak. Absorption: Z > Y X. α = 1.604–1.626 β = 1.626–1.654 γ = 1.637–1.663 2V(meas.) = ∼70◦ Cell Data: Space Group: P 21/c. a = 7.144(1) b = 7.278(1) c = 7.228(1) β = 120.50(1)◦ Z=2 X-ray Powder Pattern: Werfen, Austria; nearly identical to scorzalite. 3.23 (100), 3.20 (59), 3.14 (55), 3.077 (42), 4.73 (18), 2.548 (18), 1.571 (18) Chemistry: (1) (2) (1) (2) P2O5 45.79 44.64 FeO 3.95 11.30 TiO2 0.20 MgO 10.38 6.34 Al2O3 32.49 32.06 CaO 0.06 Fe2O3 0.60 H2O 6.48 5.66 Total 99.95 100.00 (1) Graves Mountain, Georgia, USA.
    [Show full text]
  • Prepublished Article
    1 New arsenate minerals from the Arsenatnaya fumarole, Tolbachik volcano, Kamchatka, 2 Russia. VIII. Arsenowagnerite, Mg2(AsO4)F 3 4 Igor V. Pekov1*, Natalia V. Zubkova1, Atali A. Agakhanov2, Vasiliy O. Yapaskurt1, Nikita V. 5 Chukanov3, Dmitry I. Belakovskiy2, Evgeny G. Sidorov4 and Dmitry Yu. Pushcharovsky1 6 7 1Faculty of Geology, Moscow State University, Vorobievy Gory, 119991 Moscow, Russia 8 2Fersman Mineralogical Museum of Russian Academy of Sciences, Leninsky Prospekt 18-2, 9 119071 Moscow, Russia 10 3Institute of Problems of Chemical Physics, Russian Academy of Sciences, 142432 11 Chernogolovka, Moscow Oblast, Russia 12 4Institute of Volcanology and Seismology, Far Eastern Branch of Russian Academy of Sciences, 13 Piip Boulevard 9, 683006 Petropavlovsk-Kamchatsky, Russia 14 *E-mail: [email protected] 15 16 Running title: Arsenowagnerite, a new mineral 17 18 Abstract 19 A new mineral arsenowagnerite Mg2(AsO4)F, the arsenate analogue of wagnerite, was found in 20 sublimates of the Arsenatnaya fumarole at the Second scoria cone of the Northern Breakthrough 21 of the Great Tolbachik Fissure Eruption, Tolbachik volcano, Kamchatka, Russia. It is closely 22 associated with johillerite, tilasite, anhydrite, hematite, fluorophlogopite, cassiterite, 23 calciojohillerite, aphthitalite, and fluoborite. Arsenowagnerite occurs as equant to tabular crystals 24 up to 1 mm across combined in interrupted crusts up to 0.1 x 1.5 x 3 cm. The mineral is 25 transparent, light yellow, lemon-yellow, greenish-yellow or colourless and has a vitreous lustre. 26 Arsenowagnerite is brittle, with Mohs’ hardness of ca 5. Cleavage is distinct, the fracture is –3 27 uneven. Dcalc = 3.70 g cm .
    [Show full text]
  • Hand-Book of Valuable Minerals : What They Are! What They
    TN ZGO ■H -f, ' & <- > > «.v' 0 /■ ,-vv' ( 0 N C . <£, \ ^ ^ ✓ <7* . • o \* , ■ - A - *& 0N • ' +*■ V* ;.' ** U. ■ •jopuag sapjg pajiun ‘KVItaOO d V 'non •ojouugBg jo pog 8INJO JoX8Ajns-x9 uaif.vvBi ‘(TiaiaaVAY XIAYCia •>[UEtf ibuoijb^ I'Bjuoaixioo juopTsajg ‘KOSSOYf 'a aHa'IIAY ‘DO “.Ji\r ppiuoQOK-nBjCg puu ifjpuno^ aJOuix^Bg qjnog ‘qoBg pmon*K sjajupBjnuupi aopajig ‘J9[py cy quBjg J° ‘aXVaa MOItCHOS •ipxa- Jnoijj put? ujoq -gojg-xa ‘euog y jjbj -ft i jo ‘gavj y Aaxail ‘KvaanAv v svitoiu ■a ‘a 'A 'O J° Pn« ‘3I8!IiB0 JO jgn?g pmoijVK ejm?qoj9j\[ ‘qnBg jieodag apipBo aqg, jojoajig ‘ 03 piiBq BqBino g juopisajg-ODpv ‘ Kd loi«!lJ«0 JO sjpoAY J«0 iuopisoaj ‘aa3S0a II f •ja^AVBg ‘HKia a saaavno ■00 BBaadxg -g -fi -jdng pjaiiao ‘ipojY ayo^ ‘XXVIJ '3 AaX3II •00 y ujoqaauog h jo ‘itnvaaaaxvit anoitAas •00 y pujo uipbiv jo ‘auo xaaaio at ■sojg AVBqg jo ‘AYVHS 'a KIIOI1 'Bia ‘3HIAe8niT?0 J° qnBg iBnotjujq; jsjig juapisaag-aoiA l'«A 'AY ‘jnouipaij jo quBg [«aoji*X jsaij juapisaag-aoiA ‘NVdiaaHS KIIOI' pit jo eojBSaiaa jo oauou joqBodg xo ijoXa\t?o *anHS<m at aoaoao uaamSna suijiuhuoo aixuts 'ii aoiaaaaaa •quBg oSuBqoxg ibhoijb^ pnB Ijaioog aiqBjmbg aaora -ijp?g aqjL ‘jog uoiue^aK Jopaaig -oq y pjojoa jo ‘<1110X3(1 a a •00 poQ oBuiojog jajusBOJj, pnB ‘quBg uoing [buoiybm jopaaig l-oo (Boo ^iiba a8ojO spSaoao pnt? uopBg juapisajj l °o uosuay 2? uBpuaqg ‘qoBia poppajd ‘govaa aaoaAYvao 'll •qtiBg iBUOijBjyi iBjnonijuoo jojoaaig ‘03 J9>pbjo uopbiy d soiuBp juapissij cX0SVH 'a SaitVf •XuBdraoo jBoquiBOjg JOAig jajsoqo juopisojg ‘(1331jaYAY 303030 ,fiilJoAY
    [Show full text]
  • MINERALOGY of TRIPLITE E. Wn. Hnrnucu, Uniaersity of Michigan, Ann Arbor, Michigan
    MINERALOGY OF TRIPLITE E. Wn. HnrNucu, Uniaersity of Michigan, Ann Arbor, Michigan AssrRAcr Triplite, previously treated as a divariant series between Fe" and Mn", may also contain relatively large amounts of Mg and lesser amounts of Ca. Variation in Fe and Mg is the primary factor influencing the optical properties, but Mn variation has little effect. Three new analyses of Colorado triplites are presented; two are high in Mg. Apparently the only valid species formed through weathering of triplite are dufrenite, vivianite, and phosphosiderite. Alluaudite and apatite form by reaction with solutions. Nearly 80 triplite localities have been recorded. Triplite occurs in four types of granitic pegmatites and three types of hydrothermal, high temperature veins. INtnopucrroN Previous to the work of Hurlbut (1936) triplite generally was regarded as consisting of an isomorphous seriesof two elements, ferrous iron and manganese.Analyses of triplite containing important amounts of mag- nesium were rare, and usually no consideration was given to the element in attempting to relate physical properties to composition (Henderson, 1928, Otto, 1936,and Richmond, 1940).As a result of a study of the pegmatitesof Eight Mile Park, Fremont County, Colorado,the writer described several new triplite discoveries (Heinrich, 1948). Rough crys- tals of triplite from one of these occurrenceswere measuredby Wolfe and Heinrich (1947). Qualitative tests indicated that the magnesium con- tents of these triplites might be abnormally large and that complete chemical analyses would be desirable. The writer is indebted to the Faculty Research Fund of the Rackham Graduate School, University of Michigan, for a generousgrant defraying the cost of the analysesand other expenses.Thanks are due to Professor Clifford Frondel of the De- partment of Mineralogy and Petrography, Harvard University, and to Professor Brian Mason of the Department of Geology, Indiana Uni- versity, for critical examinations of the manuscript and for suggestions toward its improvement.
    [Show full text]