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Mineralogy and Geochemistry of Nephrite Jade from Yinggelike Deposit, Altyn Tagh (Xinjiang, NW China)
minerals Article Mineralogy and Geochemistry of Nephrite Jade from Yinggelike Deposit, Altyn Tagh (Xinjiang, NW China) Ying Jiang 1, Guanghai Shi 1,* , Liguo Xu 2 and Xinling Li 3 1 State Key Laboratory of Geological Processes and Mineral Resources, China University of Geosciences, Beijing 100083, China; [email protected] 2 Geological Museum of China, Beijing 100034, China; [email protected] 3 Xinjiang Uygur Autonomous Region Product Quality Supervision and Inspection Institute, Xinjiang 830004, China; [email protected] * Correspondence: [email protected]; Tel.: +86-010-8232-1836 Received: 6 April 2020; Accepted: 6 May 2020; Published: 8 May 2020 Abstract: The historic Yinggelike nephrite jade deposit in the Altyn Tagh Mountains (Xinjiang, NW China) is renowned for its gem-quality nephrite with its characteristic light-yellow to greenish-yellow hue. Despite the extraordinary gemological quality and commercial significance of the Yinggelike nephrite, little work has been done on this nephrite deposit, due to its geographic remoteness and inaccessibility. This contribution presents the first systematic mineralogical and geochemical studies on the Yinggelike nephrite deposit. Electron probe microanalysis, X-ray fluorescence (XRF) spectrometry, inductively coupled plasma mass spectrometry (ICP-MS) and isotope ratio mass spectrometry were used to measure the mineralogy, bulk-rock chemistry and stable (O and H) isotopes characteristics of samples from Yinggelike. Field investigation shows that the Yinggelike nephrite orebody occurs in the dolomitic marble near the intruding granitoids. Petrographic studies and EMPA data indicate that the nephrite is mainly composed of fine-grained tremolite, with accessory pargasite, diopside, epidote, allanite, prehnite, andesine, titanite, zircon, and calcite. Geochemical studies show that all nephrite samples have low bulk-rock Fe/(Fe + Mg) values (0.02–0.05), as well as low Cr (0.81–34.68 ppm), Co (1.10–2.91 ppm), and Ni (0.52–20.15 ppm) contents. -
Descriptive Mineralogy
Descriptive Mineralogy Oxides and Hydroxides Classification of the Minerals • Non-Silicates • Silicates – Native Elements – Orthosilicates – Halides – Sorosilicates – Sulfides – Cyclosilicates – Oxides – Chain Silicates – Hydroxides – Layer Silicates – Carbonates – Tektosilicates – Sulfates – Phosphates Simple Oxides • Hemioxides • Sesquioxides – Cuprite (Cu O) 2 – Corundum (Al2O3) – Ice (H O) 2 – Hematite (Fe2O3) • Monoxides – Bixbyite (Mn2O3) – Periclase (MgO) • Dioxides – Wüstite (FeO) – Rutile (TiO2) – Manganosite (MnO) – Anatase (TiO2) – Lime (CaO) – Brookite (TiO2) – Zincite (ZnO) – Cassiterite(SnO2) – Bromellite (BeO) – Pyrolusite(MnO2) – Tenorite (CuO) Simple Oxides Hemi-Oxides (M2O) • Ice (H2O) Hexagonal • Cuprite (Cu2O) • Why not Na2O? – (Na radius too large) Cuprite Cu2O • Occurrence: Low Temp Hydrothermal (Supergene) • Use: Minor ore of Cu Ice H2O Crystal System Hexagonal Point Group 6/mmm Space Group P63/mmc Optical Uniaxial Color Colorless Luster Vitreous Hardness 1.5 Density 0.95 Ice H2O Ice H2O Ice H2O High Pressure Phase Diagram Monoxides (MO) • Rocksalt oxides – Periclase MgO - Wüstite FeO – Manganosite MnO – Lime CaO – Bunsenite NiO • Zincite oxides: – Zincite ZnO, – Bromellite BeO • Other monoxides: – TenoriteCuO, Montroydite HgO Rocksalt Oxides MgO-FeO-MnO-CaO Crystal System Cubic Point Group 4/m-32/m Space Group Fm3m Optical Isotropic Periclase - Wüstite MgO - FeO Lower mantle phase Mg2SiO4 = MgSiO3 + MgO Ringwoodite = Perovskite + periclase Periclase MgO Sesquioxides (M2O3) • Corundum Group – Corundum Al2O3 – Hematite -
Experimental Early Crystallization of K-Feldspar in Granitic Systems. Implications on the Origin of Magmatic Fabrics in Granitic Rocks
Geologica Acta, Vol.15, Nº 4, December 2017, 261-281 DOI: 10.1344/GeologicaActa2017.15.4.2 J. Díaz-Alvarado, 2017 CC BY-SA Experimental early crystallization of K-feldspar in granitic systems. Implications on the origin of magmatic fabrics in granitic rocks J. DÍAZ-ALVARADO1 1Departamento de Geología. Universidad de Atacama Copayapu 485, Copiapó, Chile. E-mail: [email protected] ABS TRACT One of the most outstanding characteristics of some granodioritic to granitic rocks is the presence of K-feldspar megacrysts. For instance, granodiorites and monzogranites of the Spanish Central System batholith present variable amounts of large (up to 10cm in length) euhedral K-feldspar crystals. The porphyritic textures, the euhedral shape, the alignment of plagioclase and biotite inclusions and the magmatic fabrics point to a magmatic origin for these megacrysts. This work presents a phase equilibria study in a high-K2O granodioritic system. A series of experiments were conducted with a granodioritic composition (GEMbiot) to study the crystallization sequence at the emplacement conditions in the Gredos massif, i.e. 4 H2O wt.% and 0.4GPa. Experimental results show that orthopiroxene is the liquidus phase at 1010ºC, which reacts with the H2O-rich melt to stabilize biotite between 980 and 940ºC. Plagioclase crystallizes at around 910ºC, and K-feldspar crystallizes in the matrix between 750 and 700ºC when the crystal fraction is around 0.5. However, at 850ºC, a pelite-doped experiment shows euhedral K-feldspar (≈5vol%) in both the reactive xenolith domain together with cordierite and the granodioritic domain, where the K2O wt.% rose from 4.5 in the normal experiment to 5.9 in the doped experiment. -
TEM-HRTEM Study on the Dehydration Process of Nanostructured Mg-Ca 3 4 5 Hydroxide Into Mg-Ca Oxide 6 7 8 L.S
*Manuscript Click here to view linked References 1 2 TEM-HRTEM study on the dehydration process of nanostructured Mg-Ca 3 4 5 hydroxide into Mg-Ca oxide 6 7 8 L.S. Gomez-Villalba1*, A. Sierra-Fernandez1,2 , M.E. Rabanal2,3 R.Fort1 9 10 11 1 Instituto de Geociencias (CSIC, UCM), Calle José Antonio Novais 12, 28040 Madrid, Spain 12 13 14 2 Materials Science and Engineering Department Universidad Carlos III de Madrid, Avda. 15 16 17 Universidad 30, 28911 Leganés, Madrid, Spain 18 19 20 3 Instituto Tecnológico de Química y Materiales Alvaro Alonso Barba (IAAB) , Avda. 21 22 Universidad 30, 28911 Leganés, Madrid, Spain 23 24 25 26 KEYWORDS: Nanoparticles, crystal growth, defects, HRTEM, EELS, SAED, radiolysis. Brucite, 27 28 periclase 29 30 31 * Corresponding author: Luz Stella Gomez-Villalba [email protected], 32 33 34 [email protected] 35 36 37 38 Abstract 39 40 41 The dehydration process from Mg 0.97Ca0.03 (OH)2 nanoparticles (brucite type hexagonal 42 43 44 structure) to Mg0.97Ca0.03 O (periclase type cubic structure) was studied by Transmission 45 46 Electron Microscopy (TEM-HRTEM), Electron Diffraction (SAED), EELS spectroscopy (EELS) and 47 48 image analysis. The transformation process was monitored in function of the reaction time 49 50 51 applying 200 and 300 KV. Changes in porosity were possible to observe only during the 52 53 irradiation with 200 KV. Depending on the irradiation time, the changes were gradual, 54 55 producing an increase from the particle´s edge towards the inner region. Different stages were 56 57 58 observed, corresponding to the amount of water extracted from the particle, until finally a 59 60 decrease in porosity and particle shrinkage occurs, coinciding with the formation of the Mg-Ca 61 62 1 63 64 65 oxide. -
Lower Mantle Hydrogen Partitioning Between Periclase and Perovskite: a Quantum Chemical Modelling
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Archivio istituzionale della ricerca - Università di Palermo Available online at www.sciencedirect.com ScienceDirect Geochimica et Cosmochimica Acta 173 (2016) 304–318 www.elsevier.com/locate/gca Lower mantle hydrogen partitioning between periclase and perovskite: A quantum chemical modelling Marcello Merli a, Costanza Bonadiman b, Valeria Diella c, Alessandro Pavese c,d,⇑ a Department of Earth and Marine Sciences, University of Palermo, Via Archirafi 36, 90123 Palermo, Italy b Department of Physics and Earth Sciences, University of Ferrara, Via Saragat 1, 44122 Ferrara, Italy c Consiglio Nazionale delle Ricerche, CNR-IDPA, Section of Milan, Via Mangiagalli 34, 20133 Milan, Italy d Department of Earth Sciences ‘‘A. Desio”, University of Milan, Via Botticelli 23, 20133 Milan, Italy Received 2 April 2015; accepted in revised form 27 October 2015; available online 6 November 2015 Abstract Partitioning of hydrogen (often referred to as H2O) between periclase (pe) and perovskite (pvk) at lower mantle conditions (24–80 GPa) was investigated using quantum mechanics, equilibrium reaction thermodynamics and by monitoring two H-incorporation models. One of these (MSWV) was based on replacements provided by Mg2+ M 2H+ and Si4+ M 4H+; while 2+ 3+ + 4+ 3+ + the other (MSWA) relied upon substitutions in 2Mg M Al +H and Si M Al +H .H2O partitioning in these phases was considered in the light of homogeneous (Bulk Silicate Earth; pvk: 75%–pe:16% model contents) and heterogeneous (Layered Mantle; pvk:78%–pe:14% modal contents) mantle geochemical models, which were configured for lower and upper bulk water contents (BWC) at 800 and 1500 ppm, respectively. -
The Upper Mantle and Transition Zone
The Upper Mantle and Transition Zone Daniel J. Frost* DOI: 10.2113/GSELEMENTS.4.3.171 he upper mantle is the source of almost all magmas. It contains major body wave velocity structure, such as PREM (preliminary reference transitions in rheological and thermal behaviour that control the character Earth model) (e.g. Dziewonski and Tof plate tectonics and the style of mantle dynamics. Essential parameters Anderson 1981). in any model to describe these phenomena are the mantle’s compositional The transition zone, between 410 and thermal structure. Most samples of the mantle come from the lithosphere. and 660 km, is an excellent region Although the composition of the underlying asthenospheric mantle can be to perform such a comparison estimated, this is made difficult by the fact that this part of the mantle partially because it is free of the complex thermal and chemical structure melts and differentiates before samples ever reach the surface. The composition imparted on the shallow mantle by and conditions in the mantle at depths significantly below the lithosphere must the lithosphere and melting be interpreted from geophysical observations combined with experimental processes. It contains a number of seismic discontinuities—sharp jumps data on mineral and rock properties. Fortunately, the transition zone, which in seismic velocity, that are gener- extends from approximately 410 to 660 km, has a number of characteristic ally accepted to arise from mineral globally observed seismic properties that should ultimately place essential phase transformations (Agee 1998). These discontinuities have certain constraints on the compositional and thermal state of the mantle. features that correlate directly with characteristics of the mineral trans- KEYWORDS: seismic discontinuity, phase transformation, pyrolite, wadsleyite, ringwoodite formations, such as the proportions of the transforming minerals and the temperature at the discontinu- INTRODUCTION ity. -
Epidote-Bearing Calc-Alkalic Granitoids in Northeast Brazil
Revista Brasileira de Geociências 20(1-4): 88-100, março/dezembro de 1990 EPIDOTE-BEARING CALC-ALKALIC GRANITOIDS IN NORTHEAST BRAZIL ALCIDES NÓBREGA SIAL* RESUMO GRANITÓIDES COM EPÍDOTO MAGMÁTICO NO NORDESTE DO BRASIL. Um grande número de granitóides cálcio-alcalinos com epidoto são encontrados no Domínio Estrutural Central (DEC) - que compreende três segmentos: Seridó, Cachoeirinha-Salgueiro e Riacho do Pontal - e em algu- mas outras localidades no Nordeste do Brasil. No cinturão Cachoerinha-Salgueiro (CCS), granodioritos e tonalitos com epidoto, meta a peraluminosos, intrudiram fllitos há cerca de 620 Ma, enquanto no Seridó, uma maior variedade de plutões com epfdoto fgneo intrudiu gnaisses Jucurutu ou xistos Seridó. Granodio- ritos com duas micas com (±) granada e epfdoto ígneo (?) intrudiram metassedimentos do Cinturão Riacho do Pontal. Epídoto magmático está também presente nos plutões trondhjemítícos e shoshonítícos - que in- trudiram, respectivamente, xistos Salgueiro e rochas de embasamento ao longo do limite sul do CCS - bem como em plutões no Complexo Surubim-Caroalina e nos cinturões Pajed-Paraíba e Sergipano. E encontra- do em quatro relações texturais, duas das quais indiscutivelmente magmáticas, e duas outras de reações sub- solidus. No CCS, granitóides com epfdoto solidificaram-se geralmente em torno de 6 kbar - 7 kbar, de acor- do com seus teores de Al na homblenda. Pressões mais baixas obtidas para encraves quartzo - dioríticos são devidas à perda de Al através de reação subsolidus com plagioclásio, produzindo epídoto granular. Diferem de granitóides mesozóicos similares na América do Norte porque, embora suas pressões de solidificação se- jam altas, eles intrudiram tanto metassedimentos da fácies xistos verdes como plutões paleozóicos na Argen- tina (Cadeias Pampeanas), Nova Inglaterra (área de Sherbrooke-Lewiston) e Nova Zelândia (Cadeia de Vi- tória). -
Ferropericlase – a Lower Mantle Phase in the Upper Mantle
FERROPERICLASE – A LOWER MANTLE PHASE IN THE UPPER MANTLE Gerhard P. Brey1, Vadim Bulatov2, Andrei Girnis3, Jeff W. Harris4,1, Thomas Stachel 5,1 1University of Frankfurt, Germany; 2Vernadsky Institute, Moscow, Russia; 3IGEM, Moscow, Russia; 4University of Glasgow, UK; 5University of Alberta, Edmonton, Canada INTRODUCTION was stable together with olivine, spinel (chromite, magnetite) and a Na-bearing phase, in our case melt. Ferropericlase is a major constituent of the Earth. It Only in the subsolidus run at 50 kbar and 1300 oC, a resides mainly in the lower mantle below the 670 km hitherto unknown Na- and Cr-rich phase grew. In order discontinuity, where it becomes stable through the to generate large amounts of periclase, the bulk decomposition of silicate spinel via the reaction MgO:SiO2 was chosen to 2.5 in experiments at 1300- o o Mg2SiO4 -> MgSiO3(perov) + MgO(Fe-Per). Minor 1400 C and 4.0 at 1600 C. The mixtures were prepared amounts of periclase occur also in the earth's crust, from crystalline jadeite and fired oxide mixtures of where it forms in high-temperature contact NaCrSi2O6 and NaFeSi2O6 composition added in metamorphic processes. A considerable gap in its appropriate amounts to crystalline MgO. The two latter occurrence is the upper mantle and the transition zone mixtures were fired at ~900oC in air, which provided a where the above reaction lies to the left and MgO is not highly oxidized state. The experiments were carried out stable in the presence of pyroxene. Thus, when Fe-Per under dry conditions in a belt apparatus at 30 and 50 was found as inclusion in diamonds, it was considered kbar and 1300, 1400 and 1600oC. -
A Contribution to the Crystal Chemistry of Ellestadite and the Silicate Sulfate
American Mineralogist, Volume 67, pages 90-96, I9E2 A contribution to the crystal chemistry of ellestaditeand the silicate sulfate apatitest RolnNo C. RousB Departmentof GeologicalSciences University of Michigan Ann Arbor, Michigan 48109 euo PEtp J. DUNN Departmentof Mineral Sciences Smiths o nian Inst itution Washington,D. C. 20560 Abstract A seriesof calcium silicate sulfate apatitesfrom Crestmore,California, which contain the coupled substitutionSilvsvl for 2Pv, has been investigatedusing electron microprobe, powder diffraction, and single-crystal diffraction methods. Chemical analysis of eighteen specimensof differentphosphorus contents proves that the Si:S ratio is essentiallyI : I and yieldsthe idealizedgeneral formula Caro(SiOn):-*(SO4)3-^@O4)2.(OH,F,CD2,where x : 0 to 3. The membersof this seriesfor which x : 0 and 3l2 have beenlabelled "ellestadite" and "wilkeite", respectively, by previous workers. "Ellestadite" is actually a solid solutioninvolving the end-membersCale(SiO a,){SOq)tZz, where Z: OH (hydroxylellesta- dite), F (fluorellestadite),or Cl (chlorellestadite).The term ellestaditeis redefinedto make it a group name for all compositions having >(Si,S) > P. Wilkeite is not a valid mineral species,since it is only one of many solid solutions involving the six end-members fluorapatite,hydroxyapatite, chlorapatite, fluorellestadite, hydroxylellestadite, and chlor- ellestadite. Although natural hydroxylellestadite is monoclinic, precession photographs of type "ellestadite" and "wilkeite" show hexagonalsymmetry and no evidenceof Si-S ordering as suggestedby the Si: S ratio of I : I . The silicate sulfate apatites from Crestmore show a strong linear relationshipbetween their P and F contents,such that these two variables simultaneouslygo to zero. Linear relationshipsalso exist betweentheir unit cell parame- ters and their P, F, and (Si+S) contents.These correlations imply a convergenceof the Crestmore apatite series towards a hypothetical member-of composition Caro(SiOa)r (SO4)3(OH,CI)zand cell constantsa:9.543 and c = 6.9174. -
Reading Notes on KKV Ch 2: the Interior of the Earth 2.1 EQ
Reading notes on KKV Ch 2: The interior of the earth 2.1 EQ SEISMOLOGY seismic waves, their speed double couple model and focal mechanisms. elastic rebound theory --EXPLAIN how the fault plane and auxiliary plane are different than a fault plane and its conjugate seismic tomography - like medical xrays - an energy source, illuminates the volume, and detected on the other side. in medical you know the energy and the distance travelled - all delays and attenuation of energy arrival at the detector can be attributed to complex paths and rigidity of materials. in earth, beat down the uncertainties by using more and more earthquakes and more and more stations. tomography techniques typically use one type of wave at a time. For body waves (p and s) use travel time, better for deeper imaging of velocity structure. surface waves can be better for picking up anisotropy and shorter wavelength changes. Iterative - between velocity structure and raypath. this process improves earthquake location and magnitude estimation. 2.2 VELOCITY STRUCTURE OF THE EARTH Moho was discovered in 1909. Key observation was that at 200 km from epicenter, p-wave arrivals were before predicted because the crustal paths were at 5.6 km/s and the mantle speed was 7.9 km/s. calculated depth was 54 km. same pattern is found globally - strong velocity contrast from 5.5-6 to 8 km/s at depths of 20 (new cont or rift) -80 (Himalaya) km. mean 40 km. Made my own diagram - purple is direct wave. red is a path to a station near the epicenter pink is a path to a station farther from epicenter. -
Experimental Investigations of the Reaction Path in the Mgo–CO2
Available online at www.sciencedirect.com Applied Geochemistry Applied Geochemistry 23 (2008) 1634–1659 www.elsevier.com/locate/apgeochem Experimental investigations of the reaction path in the MgO–CO2–H2O system in solutions with various ionic strengths, and their applications to nuclear waste isolation Yongliang Xiong *, Anna Snider Lord Sandia National Laboratories, Carlsbad Programs Group, 4100 National Parks Highway, Carlsbad, NM 88220, USA1 Received 26 June 2007; accepted 25 December 2007 Editorial handling by Z. Cetiner Available online 9 February 2008 Abstract The reaction path in the MgO–CO2–H2O system at ambient temperatures and atmospheric CO2 partial pressure(s), especially in high-ionic-strength brines, is of both geological interest and practical significance. Its practical importance lies mainly in the field of nuclear waste isolation. In the USA, industrial-grade MgO, consisting mainly of the mineral peri- clase, is the only engineered barrier certified by the Environmental Protection Agency (EPA) for emplacement in the Waste Isolation Pilot Plant (WIPP) for defense-related transuranic waste. The German Asse repository will employ a Mg(OH)2- based engineered barrier consisting mainly of the mineral brucite. Therefore, the reaction of periclase or brucite with car- bonated brines with high-ionic-strength is an important process likely to occur in nuclear waste repositories in salt forma- tions where bulk MgO or Mg(OH)2 will be employed as an engineered barrier. The reaction path in the system MgO–CO2– H2O in solutions with a wide range of ionic strengths was investigated experimentally in this study. The experimental results at ambient laboratory temperature and ambient laboratory atmospheric CO2 partial pressure demonstrate that hyd- romagnesite (5424) (Mg5(CO3)4(OH)2 Á 4H2O) forms during the carbonation of brucite in a series of solutions with differ- ent ionic strengths. -
List of Abbreviations
List of Abbreviations Ab albite Cbz chabazite Fa fayalite Acm acmite Cc chalcocite Fac ferroactinolite Act actinolite Ccl chrysocolla Fcp ferrocarpholite Adr andradite Ccn cancrinite Fed ferroedenite Agt aegirine-augite Ccp chalcopyrite Flt fluorite Ak akermanite Cel celadonite Fo forsterite Alm almandine Cen clinoenstatite Fpa ferropargasite Aln allanite Cfs clinoferrosilite Fs ferrosilite ( ortho) Als aluminosilicate Chl chlorite Fst fassite Am amphibole Chn chondrodite Fts ferrotscher- An anorthite Chr chromite makite And andalusite Chu clinohumite Gbs gibbsite Anh anhydrite Cld chloritoid Ged gedrite Ank ankerite Cls celestite Gh gehlenite Anl analcite Cp carpholite Gln glaucophane Ann annite Cpx Ca clinopyroxene Glt glauconite Ant anatase Crd cordierite Gn galena Ap apatite ern carnegieite Gp gypsum Apo apophyllite Crn corundum Gr graphite Apy arsenopyrite Crs cristroballite Grs grossular Arf arfvedsonite Cs coesite Grt garnet Arg aragonite Cst cassiterite Gru grunerite Atg antigorite Ctl chrysotile Gt goethite Ath anthophyllite Cum cummingtonite Hbl hornblende Aug augite Cv covellite He hercynite Ax axinite Czo clinozoisite Hd hedenbergite Bhm boehmite Dg diginite Hem hematite Bn bornite Di diopside Hl halite Brc brucite Dia diamond Hs hastingsite Brk brookite Dol dolomite Hu humite Brl beryl Drv dravite Hul heulandite Brt barite Dsp diaspore Hyn haiiyne Bst bustamite Eck eckermannite Ill illite Bt biotite Ed edenite Ilm ilmenite Cal calcite Elb elbaite Jd jadeite Cam Ca clinoamphi- En enstatite ( ortho) Jh johannsenite bole Ep epidote