CM37 1239.Pdf
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Stillwellite-(Ce) (Ce, La, Ca)Bsio
Stillwellite-(Ce) (Ce; La; Ca)BSiO5 c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Hexagonal. Point Group: 3: As °at rhombohedral crystals, to 4 cm, and massive. Twinning: Observed about [100]. Physical Properties: Cleavage: One imperfect. Fracture: Conchoidal. Hardness = 6.5 D(meas.) = 4.57{4.60 D(calc.) = 4.67 » Optical Properties: Transparent to translucent. Color: Red-brown to pale pink; colorless in thin section. Streak: White. Optical Class: Uniaxial (+) to biaxial (+). ! = 1.765{1.784 ² = 1.780{1.787 2V(meas.) = 0±{6± Cell Data: Space Group: P 31: a = 6.841{6.844 c = 6.700{6.702 Z = 3 X-ray Powder Pattern: Mary Kathleen mine, Australia. 3.43 (s), 2.96 (s), 2.13 (ms), 4.44 (m), 1.864 (m), 2.71 (mw), 2.24 (mw) Chemistry: (1) (2) (1) (2) (1) (2) SiO2 22.40 22.06 La2O3 27.95 19.12 MgO 0.06 UO2 0.22 Ce2O3 33.15 30.82 CaO 0.95 0.34 ThO2 5.41 Pr2O3 1.82 F 0.30 + B2O3 12.23 [13.46] Nd2O3 5.36 H2O 0.85 Al2O3 0.42 Sm2O3 0.34 H2O¡ 0.10 Y2O3 0.74 0.28 Fe2O3 0.18 P2O5 0.67 Total [100.00] [99.26] (1) Mary Kathleen mine, Australia; recalculated to 100.00% after removal of very small amounts of uraninite and apatite determined by separate analysis. (2) Vico volcano, near Vetralla, Italy; by electron microprobe, B2O3 calculated from stoichiometry, original total given as 99.23%; corresponds to (Ce0:50La0:31Nd0:08Th0:05Pr0:03Ca0:02Sm0:01)§=1:00B1:02Si0:97O5: Occurrence: Locally abundant as a metasomatic replacement of metamorphosed calcareous sediments (Mary Kathleen mine, Australia); in alkalic pegmatites in syenite in an alkalic massif (Dara-i-Pioz massif, Tajikistan). -
Mineralogy and Geological Setting of Allanite-(Ce)-Pegmatites 341
NORWEGIAN JOURNAL OF GEOLOGY Mineralogy and geological setting of allanite-(Ce)-pegmatites 341 Mineralogy and geological setting of allanite-(Ce)- pegmatites in western Hurrungane, Jotun Nappe Complex, Norway: an EMP and ID-TIMS study Simon Spürgin, Rune S. Selbekk and Anders Mattias Lundmark Spürgin, S., Selbekk, R. & Lundmark, M. 2009: Mineralogy and geological setting of allanite-(Ce)- pegmatites in western Hurrungane, Jotun Nappe Complex, Norway: an EMP and ID-TIMS study. Norwegian Journal of Geology, vol. 89, pp 341-356, Trondheim 2009, ISSN 029-196X. The 950 ± 1 Ma Berdalsbandet Pegmatite Swarm (BPS) in Hurrungane, in the Jotun Nappe Complex, SW Norway, consists of ≤2 m wide subpa- rallel granitic dykes emplaced in a sinistral non-coaxial shear zone, constraining the age of local Sveconorwegian deformation. The abyssal class dyke swarm is interpreted to be related to local Sveconorwegian anatexis; mineralogy and REE characteristics indicate low degree partial melting. The pegmatites are symmetrically zoned and typically consist of an outer zone of feldspar + allanite-(Ce) + biotite, a transitional zone of feldspar + quartz + schorl + Fe-Ti-oxides, an inner zone of quartz + schorl + garnet + beryl and a core of hydrothermal quartz. A metasomatic rim of biotite is locally developed along contacts to the amphibolite wallrock. Secondary zeolites are suggested to relate to late- to post-Caledonian altera- tion. The dykes contain various rare-earth minerals, predominantly allanite-(Ce). Its composition, determined by electron microprobe (EMP) and 2+ expressed by representative analyses from three samples, is: (Ca0.86REE0.80Mn0.09Th0.01Na0.03)Σ1.79(Al1.79Fe 0.99Mg0.16Ti0.10)Σ3.04(Si3.17P0.01)O12(OH), (Ca1 2+ 3+ 2+ 3+ 0.30 .12REE0.72Mn0.03Th0.01Na0.02)Σ1.90(Al1.73Fe 0.66Fe 0.33Mg0.26Ti0.03)Σ3.01Si3.07O12(OH) and (Ca1.10REE0.74Mn0.02Th0.01Na0.01)Σ1.88(Al1.75Fe 0.69Fe 0.26Mg Ti0.04) 3+ 3+ 2+ 2+ 3+ 3+ 2+ 2+ 3+ Σ3.04Si3.08O12(OH). -
Separation of Radioactive Elements from Rare Earth Element-Bearing Minerals
metals Review Separation of Radioactive Elements from Rare Earth Element-Bearing Minerals Adrián Carrillo García 1, Mohammad Latifi 1,2, Ahmadreza Amini 1 and Jamal Chaouki 1,* 1 Process Development Advanced Research Lab (PEARL), Chemical Engineering Department, Ecole Polytechnique de Montreal, C.P. 6079, Succ. Centre-ville, Montreal, QC H3C 3A7, Canada; [email protected] (A.C.G.); mohammad.latifi@polymtl.ca (M.L.); [email protected] (A.A.) 2 NeoCtech Corp., Montreal, QC H3G 2N7, Canada * Correspondence: [email protected] Received: 8 October 2020; Accepted: 13 November 2020; Published: 17 November 2020 Abstract: Rare earth elements (REE), originally found in various low-grade deposits in the form of different minerals, are associated with gangues that have similar physicochemical properties. However, the production of REE is attractive due to their numerous applications in advanced materials and new technologies. The presence of the radioactive elements, thorium and uranium, in the REE deposits, is a production challenge. Their separation is crucial to gaining a product with minimum radioactivity in the downstream processes, and to mitigate the environmental and safety issues. In the present study, different techniques for separation of the radioactive elements from REE are reviewed, including leaching, precipitation, solvent extraction, and ion chromatography. In addition, the waste management of the separated radioactive elements is discussed with a particular conclusion that such a waste stream can be -
Baddeleyite Zro2 C 2001-2005 Mineral Data Publishing, Version 1 Crystal Data: Monoclinic
Baddeleyite ZrO2 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. Crystals commonly tabular on {100} and somewhat elongated on [010], or short to long prismatic along [001], to 6 cm; rarely equant; prism faces striated k [001]; radially fibrous with concentric banding in botryoidal masses. Twinning: Ubiquitous; on {100} and {110}, both may be polysynthetic; rare on {201}. Physical Properties: Cleavage: {001} nearly perfect, {010} and {110} less perfect. Fracture: Subconchoidal to uneven. Tenacity: Brittle. Hardness = 6.5 D(meas.) = 5.40–6.02 D(calc.) = [5.83] Blue-green cathodoluminescence. Optical Properties: Transparent; in dark-colored specimens, only in thin fragments. Color: Colorless to yellow, green, greenish or reddish brown, brown, iron-black; colorless to brown in transmitted light. Streak: White to brownish white. Luster: Greasy to vitreous; nearly submetallic in black crystals. Optical Class: Biaxial (–). Pleochroism: X = yellow, reddish brown, oil-green; Y = oil-green, reddish brown; Z = brown, light brown. Orientation: X ∧ c =13◦; Y = b. Dispersion: r> v, rather strong. Absorption: X > Y > Z. α = 2.13(1) β = 2.19(1) γ = 2.20(1) 2V(meas.) = 30(1)◦ 2V(calc.) = 28◦ Cell Data: Space Group: P 21/c (synthetic). a = 5.1505(1) b = 5.2116(1) c = 5.3173(1) β =99.230(1)◦ Z=4 X-ray Powder Pattern: Phalaborwa, South Africa. 3.15 (10), 2.835 (9), 2.62 (5), 1.817 (5), 3.66 (4), 3.51 (4), 1.847 (4) Chemistry: (1) (2) (1) (2) (1) (2) SiO2 0.19 0.08 HfO2 0.93 CaO 0.06 TiO2 0.56 Fe2O3 0.82 LOI 0.28 ZrO2 98.90 97.8 FeO 1.3 Total 100.25 100.67 (1) Balangoda, Sri Lanka. -
Replacement of Primary Monazite by Apatite-Allanite-Epidote Coronas in an Amphibolite Facies Granite Gneiss from the Eastern Alps
American Mineralogist, Volume 83, pages 248±258, 1998 Replacement of primary monazite by apatite-allanite-epidote coronas in an amphibolite facies granite gneiss from the eastern Alps FRITZ FINGER,IGOR BROSKA,* MALCOLM P. ROBERTS, AND ANDREAS SCHERMAIER Institut fuÈr Mineralogie der UniversitaÈt Salzburg, Hellbrunnerstrasse 34, A-5020 Salzburg, Austria ABSTRACT Accessory monazite crystals in granites are commonly unstable during amphibolite fa- cies regional metamorphism and typically become mantled by newly formed apatite-allan- ite-epidote coronas. This distinct textural feature of altered monazite and its growth mech- anism were studied in detail using backscattered electron imaging in a sample of metagranite from the Tauern Window in the eastern Alps. It appears that the outer rims of the former monazites were replaced directly by an apatite ring with tiny thorite inter- growths in connection with Ca supply through metamorphic ¯uid. Around the apatite zone, a proximal allanite ring and a distal epidote ring developed. This concentric corona struc- ture, with the monazite core regularly preserved in the center, shows that the reaction kinetics were diffusion controlled and relatively slow. Quantitative electron microprobe analyses suggest that the elements released from mon- azite breakdown (P, REE, Y, Th, U), were diluted and redistributed in the newly formed apatite, allanite, and epidote overgrowth rings and were unable to leave the corona. This supports the common hypothesis that these trace elements are highly immobile during metamorphism. Furthermore, microprobe data suggest that the preserved monazite cores lost little, possibly none of their radiogenic lead during metamorphism. Thus, metastable monazite grains from orthogneisses appear to be very useful for constraining U-Th-Pb protolith ages. -
159.Pdf by Guest on 02 October 2021 T60 TIIE CANADIAN MINERALOGIST
1.59 CanadianMineralogist Vol.3l, pp. 159-166(1993) THERARE.EARTH.ELEMENT CHEMISTRY OF ALLANITE FROMTHE GRENVILLE PROVINCE RONALD C. PETERSONANDDARRYLB. MacFARLANE* DepartmzntofGeological Sciences, Queen's University, Kingstoa Ontario K7L 3N6 ABSTRACf The resultsof electron-microprobeanalyses of 38 samplesof allanite from granitic rocks and calcite veins in the Grenville provinceof southeastemOntario'and southwestem Quebec are presented. Allanite from granitic rocksshow a w.iderrang e o!ffn contentsthanttrosefromcarbonateveins.Thesamplesofallanitestudiedexhibitthecoupledsolid-solutionCa nZ* + IvP*as well asan omission solid-solution of theform 3Cazn=2REP* +n' Keywords:allanite, epidote group, electron-microprobe analysis, solid solution,Grenville Province,Ontario, Quebec. SoNaMerns Nouspr6sentons les r6sultatsd'analyses i la microsonde6lectronique de trenre-huit 6chantillons d'allanite provenantde r@hes granitiqueset de filoni de calcite dansia provincedu Grenville, dansie sud-estde l'Ontario et le sud-ouestdu Qu6bec.L'allanite desroches granitiques montre une qlus gonde variabilit6 entenews de teres rates(7R) quecelle des de^carbonate' ir6lev6e frloqs = + n, La solutionsolide coupl6e Ca2+ + Al3+ * p"3+-ip3+ + M2' et tn m&anismeimpliquant une lacune,comm e 3Ca'* 2TR3* rendentcompte de la compositiondes &hantillons. (*aduit par la R6daction) Mots-cl€s:allanite, groupede f6pidote, analysesd la microsonde6lectronique, solution solide,province du Grenville' Ontario, Qudbec. INTRODU(NON plex unzonedpegmatites. Although allanite is found in all four types,it is particularlyabundant in simplezoned pegmatitesin the vicinity of Bancroft and Madawaska' Allanite-(Ce), which has, as idealized formula bntarlo. In this area,individual crystalsup to 60 cm in (Ce,Ca"Y)z(Al,Fe3+)3(SiOr3(OH),is the most abundant length and 15 cm in width havebeen reported (Hogarth and widespread rare-earth-element-bearingmineral et aL 1983),Allanite also occurs as an accessorymineral found in the Grenville hovince of the CanadianShield. -
Västmanlandite-(Ce) – a New Lanthanide- and F-Bearing Sorosilicate Mineral from Västmanland, Sweden: Description, Crystal Structure, and Relation to Gatelite-(Ce)
Eur. J. Mineral. 2005, 17, 129–141 Västmanlandite-(Ce) – a new lanthanide- and F-bearing sorosilicate mineral from Västmanland, Sweden: description, crystal structure, and relation to gatelite-(Ce) DAN HOLTSTAM1, UWE KOLITSCH2 and ULF B. ANDERSSON3 1Sektionen för mineralogi, Naturhistoriska riksmuseet, Box 50007, SE-104 05 Stockholm, Sweden Corresponding author, e-mail: [email protected] 2Institut für Mineralogie und Kristallographie, Universität Wien, Geozentrum, Althanstraße 14, A-1090 Wien, Austria 3Institutionen för geovetenskaper, Uppsala Universitet, Villavägen 16, SE-752 36 Uppsala, Sweden Abstract: Västmanlandite-(Ce), ideally (Ce,La)3CaAl2Mg2[Si2O7][SiO4]3F(OH)2, is a new mineral species from the Västmanland county, Bergslagen region, Sweden. Together with more Fe-rich, F-poor members, it forms solid solutions that are important for lanthanide sequestration in the Bastnäs-type skarn deposits in Västmanland. At the type locality (Malmkärra, Norberg district) it occurs as anhedral grains 0.2–3 mm across, in association with fluorbritholite-(Ce), tremolite, a serpentine mineral, magnetite, dollaseite-(Ce) and dolomite. The mineral is allanite-like in appearance; it is dark brown, translucent, with vitreous luster, and has -3 good cleavage parallel to {001}, uneven to conchoidal fracture, and a yellowish gray streak; Dcalc = 4.51(2) g·cm and Mohs hardness 6. Optically it is biaxial (-), with = 1.781(4), calc = 1.792, = 1.810(4) and 2V = 75(5)°. Chemical analysis by electron-microprobe 57 and Fe Mössbauer spectroscopy yield: La2O3 13.65, Ce2O3 23.90, Pr2O3 2.07, Nd2O3 6.28, Sm2O3 0.42, Gd2O3 0.15, Y2O3 0.18, CaO 4.65, FeO 1.14, Fe2O3 2.69, MgO 5.51, Al2O3 8.58, TiO2 0.04, P2O5 0.05, SiO2 26.61, F 1.06, H2Ocalc 1.61, O ≡ F –0.45, sum 98.14. -
ALLANITE-(Ce) and ITS ASSOCIATIONS, from the DITRAU ALKALINE INTRUSIVE MASSIF, EAST CARPATHIANS, ROMANIA
THE PUBLISHING HOUSE GEONOMY OF THE ROMANIAN ACADEMY Research article ALLANITE-(Ce) AND ITS ASSOCIATIONS, FROM THE DITRAU ALKALINE INTRUSIVE MASSIF, EAST CARPATHIANS, ROMANIA Paulina HIRTOPANU 1* , Jens C. ANDERSEN 2, Robert J. FAIRHURST 2 and Gyula JAKAB 3 1 Dept.Mineralogy, University of Bucharest, Romania 2 University of Exeter, Camborne School of Mine, UK 3 IG Mineral Gheorgheni, Romania *[email protected] Received March 27, 2013 The Ditrau alkaline intrusive complex (DAIC) is situated within the crystalline rocks of the inner part of the East Carpathians. It has a distinct ring structure and a succession of magmatic events from gabbroic and dioritic magma to syenitic and various postmagmatic events as well, developed between a Triassic extensional stage and a Jurassic rifting stage. The DAIC has a high petrographic complexity and a great diversity of mineral occurrences. More than 200 new minerals were recently identified, many of them being first occurrences in Romania. The rare element minerals which were determined in DAIC belong to the following classes, in the predominant order: I. LREE(Y)-carbonates; II. Nb, Ta, REE(Y),Ti, Zr, Th, U-oxides III.REE(Y)-Phosphates; IV. REE-(Y), Th, Zr, Pb-Silicates. Among silicates, the following minerals occur in DAIC, specially in Jolotca area: allanite-(Ce), thorite, thorogummite, cerite-(Ce), chevkinite-(Ce), törnebohmite-(Ce), stillwellite-(Ce), tritomite-(Ce), britholite-(Ce) and Th-zircon. Allanite-(Ce) occurs as a constituent mineral in mineralizing Jolotca area and as an accessory one in the rest of the massif. The chemical composition of allanite-(Ce) has high Fe 2O3 content, showing oxidizing conditions for its genesis. -
Rare Earth Element and Yttrium Mineral Occurences in the Adirondack Mountains Marian V
6 RARE EARTH ELEMENT AND YTTRIUM MINERAL OCCURENCES IN THE ADIRONDACK MOUNTAINS MARIAN V. LUPULESCU,1 JEFFREY R. CHIARENZELLI,2 AND JARED SINGER3 1. Research and Collections, New York State Museum, Albany, NY 12230, [email protected] 2. Department of Geosciences, St. Lawrence University, Canton, NY 13617 3. Department of Earth and Environmental Sciences, Rensselaer Polytechnic Institute, Troy, NY 12180 KEYWORDS: Rare Earth Elements, Yttrium, Lyon Mountain Granite, Iron Deposits, Eastern Adirondack Highlands INTRODUCTION The rare earth elements (REE), formally called lanthanides, are a set of fifteen chemical elements, from lanthanum (La) to lutetium (Lu). Yttrium (Y) is added to this group because it has similar properties and occurs in the same mineral deposits. These elements are divided into low-atomic number, lanthanum to europium (La-Eu), or light rare earth elements (LREE), and heavy-atomic number, gadolinium to lutetium (Gd-Lu), or heavy rare earth elements (HREE). Even though they are called “rare,” they are widely distributed in the Earth’s crust and are present in all types of igneous, metamorphic, and sedimentary rocks. Some of the REE have abundances (relative amount of an element in the Earth’s crust) comparable or higher than gold, mercury, tungsten, tin, arsenic, copper, cobalt, and zinc (Handbook of Chemistry and Physics, 2016). In geology research, REE are used to understand earth processes such as crystal fractionation, partial melting, magma mixing, and absolute age dating of minerals. The REE have high-tech industrial applications and are essential for making hybrid cars, computers, smartphones, color TV, lasers, ceramics, and military devices. For this reason, the United States Geological Survey identified the rare earth element dysprosium as one of the most critical elements in the 2010 Critical Materials Strategy 80 THE ADIRONDACK JOURNAL OF ENVIRONMENTAL STUDIES VOLUME 21 81 6: RARE EARTH ELEMENT AND YTTRIUM MINERAL OCCURENCES IN THE ADIRONDACK MOUNTAINS report. -
Rare Earth Element Evolution and Migration in Plagiogranites: a Record Preserved in Epidote and Allanite of the Troodos Ophiolite
Contrib Mineral Petrol (2015) 169:25 DOI 10.1007/s00410-015-1114-y ORIGINAL PAPER Rare earth element evolution and migration in plagiogranites: a record preserved in epidote and allanite of the Troodos ophiolite Michael Anenburg · Yaron Katzir · Dieter Rhede · Niels Jöns · Wolfgang Bach Received: 1 October 2014 / Accepted: 14 January 2015 © Springer-Verlag Berlin Heidelberg 2015 Abstract Plagiogranites from the Troodos ophiolite in causing crystallisation of allanite-(Y) from hydrothermal Cyprus are occasionally epidotised, either partially or com- fluids in the miarolites. The REE pattern of the hydrother- pletely. Epidotisation phenomena include replacement of mal allanite-(Y) is characterised by LREE and Eu deple- pre-existing minerals and filling of miarolitic cavities. In tion, similar to the parent plagiogranitic magma. As allan- addition to epidote, miarolites in one plagiogranite body ite had sequestered most of the REE in the fluid, epidote (located near the village of Spilia) contain coexisting fer- took over as the principle hydrothermal mineral. Epidote in riallanite-(Ce) and allanite-(Y). Textural and geochemical Troodos plagiogranites records a fluid evolutionary trend evidence indicates that late-stage REE-enriched granitic beginning with REE-rich–Eu-depleted similar to allanite- melt facilitated crystallisation of magmatic ferriallanite- (Y) and gradually transforming into the REE-depleted– (Ce). High REE contents persisted after fluid exsolution, Eu-enriched pattern prevalent throughout ‘conventional’ sub-seafloor fluids. A comparison of allanite-bearing Electronic supplementary material The online version of this and allanite-absent plagiogranites from the same local- article (doi:10.1007/s00410-015-1114-y) contains supplementary ity suggests that REE-bearing fluids migrated from the material, which is available to authorized users. -
Download the Scanned
BOOK REVIEWS TABELLBN ZUR OPTISCHEN BESTIMMUNG DER GESTEINSBILDENDEN MINERALE, By W. E. Tncicnn. xi-1147 pp., 17 tables,376 figures,2 plates in rear pocket. E. Schweizerbart'scheVerlagsbuchhandlung, Stuttgart, Germany.DM. 27.80. ($6.67)resz. Professor Triiger, of the Mineralogical Institute of the Technical University of Darm- stadt, has succeeded in providing workers in optical mineralogy and microscopic petrog- raphy with a highly useful and effective tool in his compilation, Tables for the optical de- termination of the rock forming minerals. The work is essentially without formal text, except for the introduction and an explanation of abbreviations. Most of its data are sum- marized in 6 tables: 1. Water soluble minerals. 2, Opaque or nearly opaque minerals. 3. Uniaxial or pseudocubic minerals. 4. Uniaxial tetragonal minerals. 5. Uniaxial hexagonal minerals. 6. Biaxial minerals. The last are arranged chemically under oxides, hydroxides, carbonates, sulfates, phos- phates, nesosilicates, sorosilicates, inosilicates, phyllosilicates and tectosilicates. Each table gives information under the headings: (1) Name, system, chemical composition; (2) Com- mon forms, twinning, habit, aggregate structure; (3) Cleavage, gljding, hardness, density; (4) optical orientationl (5) Refringence and birefringence; (6) Angle and dispersion of the optic axes; (7) Color in thin section, pleochroism, absorption; (8) Special diagnostic chemical characteristicsl (9) Diagnostic characteristics of similar mineralsl and (r0) Paragenesis. An amazing amount of information has been packed into the tables, although the descriptions of the parageneses are necessarily curtailed and thus somewhat over- simplified, with each of the tables are numerous figures of two types: (1) Three dimensional and sectional crystal drawings showing the optic orientation and (2) Curves relating composi- tional variation to variations in optical properties and density. -
Growth of Hydrothermal Baddeleyite and Zircon in Different Stages Of
1 Revision 2 2 Growth of hydrothermal baddeleyite and zircon in different 3 stages of skarnization 4 Wen Winston Zhao1, Mei-Fu Zhou1*, and Wei Terry Chen2 5 1 Department of Earth Sciences, The University of Hong Kong, Pokfulam Road, Hong 6 Kong, China 7 2 State Key Laboratory of Ore Deposit Geochemistry, Institute of Geochemistry, Chinese 8 Academy of Sciences, Guiyang 550002, China 9 10 11 12 13 14 15 16 17 18 ------------------------------------------------- 19 E-mail address: 20 Wen Winston Zhao: [email protected]; +852-56133681 21 Mei-Fu Zhou: [email protected]; +852-28578251 (*corresponding author) 22 Wei Terry Chen: [email protected]; +86-13710113486 1 23 ABSTRACT 24 Both prograde and retrograde skarns from the Tengtie iron deposit, South China contain 25 rounded, euhedral, and anhedral zircon grains. Rounded grains were originally derived 26 from detritus in carbonate rocks and were incorporated into the skarns. Euhedral and 27 anhedral crystals are intergrown with various skarn minerals and are clearly hydrothermal 28 in origin. These hydrothermal grains have low (Sm/La)N ratios and high La contents 29 relative to typical magmatic ones and display flat LREE and subdued flattening of HREE 30 chondrite-normalized patterns, similar to those of zircon crystallized from Zr-saturated 31 fluids. Prograde skarns also contain baddeleyite rimed by zircon, which record a period 32 of low Si activity during prograde skarnization relative to original magmatic- 33 hydrothermal fluids. Hydrothermal zircon grains from Tengtie have variable Eu 34 anomalies and slightly positive Ce anomalies, indicating that they may have crystallized 35 from highly heterogeneous, but generally reducing fluids.