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  • 1
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 109 (1992), S. 511-525 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Some of the most vanadium-rich silicate minerals known are present in green mica schist from the Hemlo gold deposit, Ontario, Canada. Vanadium-rich silicate minerals include green mica (up to 17.6 wt. % V2O3), phlogopite (10.1 wt. % V2O3), pumpellyite (25.7 wt. % V2O3), garnet (18.5 wt. % V2O3), epidote-group minerals (9.1 wt. % V2O3), antimonian vesuvianite (4.3 wt. % V2O3), and titanite (18.5 wt. % V2O5). In addition, minor amounts of V (〈2 wt. % V2O3) are present in tourmaline, chlorite, talc and tremolite in other lithologies of the Hemlo deposit. The principal substitution that incorporates V into most of these silicate minerals is Al3+=V3+ in octahedral positions. Vanadium is incorporated into phlogopite mainly by the two substitutions: 3Mg2+ =2V3++□ and VIMg2++IVSi4+=VIV3+ +IVAl3+, and all of the three substitutions Ti4++O2- =V3++(OH,F)-, Ti4+=V4+, and 5Ti4+=4V5+ +□ may have operated in titanite. Vanadium-enriched green mica schist from the Hemlo gold deposit is characterized by uniform Ti/Zr ratios, systematically low Ti, Ni, Co and Sc abundances, and low levels of incompatible elements Th, U, Hf and Zr and is distinct in these respects from its Cr-enriched counterpart. These geochemical features, along with textural evidence (relict quartz and oligoclase phenocrysts), indicate that the V-enriched green mica schist from Hemlo was most likely derived mainly from quartz-oligoclase porphyry. However, its anomalously high V and Cr contents were probably introduced metasomatically from local maficultramafic sources and were fixed in green mica and oxides during the waning of a second regional metamorphism. Vanadium was further remobilized, and its concentration probably enhanced, during the late hydrothermal alteration, which resulted in the formation of the characteristic V-rich calc-silicate minerals.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 20 (1994), S. 594-600 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract Phase relations in the system NaAlSiO4-NaGaSiO4 to 945° C at 1 kbar P(H2O) are dominated by stability of Na(Al,Ga)SiO4 with the beryllonite-type structure. The nepheline structure is restricted to NaAlSiO4-rich compositions at moderate and high temperature. Structure-composition relationships are controlled by space-fitting requirements of both framework and cavity cations, as in related systems. The two-phase (nepheline-type+beryllonite-type) field has been delineated from the end-member NaAlSiO4 composition up to the peritectic point at about 945° C (and 60 mol% NaGaSiO4), using a volume-composition relationship for the beryllonite-type phase, phase appearance, and electron microprobe analysis. At end-member NaGaSiO4 composition, the beryllonite-type phase is stable to the melting point (902±5° C). At end-member NaAlSiO4 composition, the beryllonite-type⇌nepheline-type transformation occurs at 348±2° C, and is associated with an increase in molar volume of 2.4% and enthalpy of 5170±40J·mol−1. Thus, end-member NaAlSiO4 nepheline, and probably all sub-potassic nephelines as well, are metastable at very-low geological temperatures.
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  • 4
    Publication Date: 2011-01-13
    Description: The Zaglic and Safikhanloo epithermal gold prospects are located in the Arasbaran zone, to the west of the Cenozoic Alborz-Azarbaijan magmatic belt in NW Iran. Mineralization is mainly restricted to quartz and quartz -carbonate veins and veinlets. Pyrite is the main sulphide, associated with subordinate chalcopyrite and bornite. Gold occurs as microscopic and submicroscopic grains in quartz and pyrite. The country rocks are Tertiary intermediate-mafic volcanic and volcaniclastic rocks of andesite to trachy-andesite composition intruded by a composite granitic to syenitic pluton. They are medium- to high-K, calc-alkaline and alkaline rocks and display fractionated REE (rare earth element) patterns, with light rare earth elements (LREE) significantly enriched relative to the heavy rare elements (HREE). On primitive mantle normalized plots, they display depletions in Nb, Ti and P, and enrichments in Pb, which are common characteristics of arc-related magmas worldwide. Hydrothermal alteration minerals developed in the wall rocks include quartz, calcite, pyrite, kaolinite, montmorillonite, illite, chlorite, and epidote. Minor alunite occurs in Safikhanloo. Gold is locally enriched in the altered rocks immediate to the veins. The ore-stage quartz from both prospects is dominated by liquid-rich fluid inclusions; vapour-rich inclusions are rare. The homogenization temperature varies between 170-230 and 170-330 {degrees}C and salinity varies between 1.4 to 9.5 and 〈1 to 6.7 wt% NaCl equivalent, for Safikhanloo and Zaglic, respectively. The occurrence of hydrothermal breccias, bladed calcite, adularia, and rare coexisting vapour- and liquid-dominant inclusions suggest that boiling occurred in the course of the evolution of the ore fluids. The large variations in Th and the salinity values can be explained by boiling and/or mixing. Lack of sulphate minerals in the veins suggests that sulphides and gold precipitated from a reduced, H2S-dominant fluid. Calculated {delta}34S values for the ore fluid vary between -4.6 and -9.3{per thousand}. Sulphur could have been derived directly from magmatic sources, or leached from the volcanic and plutonic country rocks. Ore formation in Zaglic and Safikhanloo occurred in response to mixing, boiling, and interactions with wall rocks. Considering the intermediate-argillic alteration, the low contents of base metal sulphides, and the overall low salinities, the Zaglic and Safikhanloo can be classified as low-sulphidation epithermal systems.
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  • 5
    Publication Date: 2016-08-25
    Print ISSN: 2469-9950
    Electronic ISSN: 2469-9969
    Topics: Physics
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  • 6
    Publication Date: 2012-02-01
    Description: Hemimorphite, a zeolite-like mineral commonly present in supergene non-sulfide Zn deposits and Zn mine tailings, is known to contain elevated levels of As, Cd, Cu and Pb. Cation-exchange experiments of a natural hemimorphite (Mapimi, Durango, Mexico) with 0.1 M CaCl2 solution at 110 ºC show that As and Cu are retained, whereas Cd and Pb are readily exchanged. The retention of As is consistent with previous single-crystal electron paramagnetic resonance (EPR) results that showed its occurrence as the substitutional As5+ ion at the Si site. Single-crystal EPR spectra of hemimorphite from the M’Fouati Pb-Zn mine (Reneville, Congo), measured at 120 K and 295 K, show a Cu2+ center. The best-fit spin Hamiltonian parameters g, A(63Cu), P (63Cu) and A(1H) of this center at 120 K demonstrate that Cu2+ resides at the tetrahedral Zn site, not in the channels as suggested by a previous powder EPR study. Cadmium and Pb in hemimorphite are probably present in the channels; this would account for their contrasting behavior from As and Cu during the cation-exchange experiments. However, single-crystal EPR spectra of ten samples of hemimorphite from various Pb-Zn deposits, including those taken after gamma-ray irradiation for doses up to 55 kGy, did not detect any paramagnetic Cd or Pb centers.
    Print ISSN: 0008-4476
    Topics: Geosciences
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  • 7
    Publication Date: 2011-01-01
    Description: Through the complementary use of single-crystal X-ray diffraction and X-ray absorption spectroscopy, we present in this paper the first direct results on the site occupancy of thorium in the fluorapatite structure and the structural distortion created by its substitution. Structure refinements based on single-crystal X-ray diffraction data from synthetic Th-doped fluorapatite indicates that Th substitutes almost exclusively in the M2 site. A single-crystal X-ray study of natural fluorapatite from Mineville, New York, also indicated that substituting heavy scatterers (including Th) are concentrated in the apatite M2 site, but definitive site assignments of specific elements were not possible. Extended X-ray absorption fine-structure spectroscopy (EXAFS) was used to probe the local structure of Th in the synthetic fluorapatite (single-crystal form) with a Th concentration of roughly 20000 ppm, as well as Th in the natural Mineville fluorapatite (powder form) with a Th concentration of ~2000 ppm. The EXAFS fitting results also indicate that Th partitions into the M2 site and yield a ~0.05-0.08 A decrease of average M2-O bond distances associated with local structure distortions that are not obtainable from single-crystal X-ray diffraction studies.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 8
    Publication Date: 2011-08-01
    Description: Synthetic stishovite before and after electron- and {gamma}-ray irradiation has been investigated by single-crystal electron paramagnetic resonance (EPR) spectroscopy for the first time. Room-temperature single-crystal EPR spectra of as-is stishovite reveal two high-spin (S = 3/2) Cr3+ centers: one with D2h symmetry and another of triclinic symmetry. Quantitatively determined spin Hamiltonian parameters, including matrices g, D, and A(53Cr) and high-spin Zeeman term BS3, suggest that the D2h center represents a substitutional Cr3+ ion at the Si site without an immediate charge compensator. The triclinic center, which is characterized by a well-resolved 1H superhyperfine structure, also arises from a substitutional Cr3+ ion at the Si site but has an H+ charge compensator bonded to one of the four equatorial oxygen atoms. The magnitude and orientation of the 1H superhyperfine structure yield the location of the H atom at (0.46, 0.12, 0). These structural models for Cr and H in stishovite also have been corroborated by periodic density functional theory (DFT) calculations using the Vienna ab initio simulation package (VASP), with 2 x 2 x 4 supercells, plane-wave basis sets and the projector augmented wave (PAW) potentials. In addition, 85 K EPR spectra of irradiated stishovite show that the two Cr3+ centers are both converted to an S = 1/2 Cr5+ center characterized by two 29Si superhyperfine structures arising from interactions with two nearest and eight second-nearest Si atoms, respectively. The spin Hamiltonian parameters of this Cr5+ center provide further support for the location of the two Cr3+ centers at the Si site.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 9
    Publication Date: 2011-06-01
    Description: World-class borate deposits in Turkey and California contain elevated concentrations of arsenic, with adverse effects to not only local suppliers of water, but also the commercial exports of boron products. Most previous studies and remediation efforts of arsenic contamination in borate deposits have focused on sulfarsenides. Inductively coupled plasma - mass spectrometry (ICP-MS) analysis and synchrotron micro-X-ray fluorescence ({micro}-SXRF) mapping reveal that colemanite, a major borate ore mineral, contains up to 125 ppm arsenic. Arsenic K-edge X-ray absorption near-edge structure (XANES) spectra suggest the presence of both As3+ and As5+ species in colemanite. The data on K-edge extended X-ray absorption fine structure (EXAFS) show preferential occupancies of As5+ and As3+ at the tetrahedral B2 site and the triangular B1 site, respectively. Single-crystal electron paramagnetic resonance (EPR) spectra of gamma-ray-irradiated colemanite measured at 40 K contain an [AsO3]2- center, providing further support for the presence of As5+. Therefore, colemanite is a significant source of arsenic contamination, not only in commercial boron products, but also aquifers associated with borate deposits.
    Print ISSN: 0008-4476
    Topics: Geosciences
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  • 10
    Publication Date: 2011-06-01
    Description: Sibirskite, parasibirskite and priceite, synthesized in aqueous solutions at temperatures from 80 to 240{degrees}C, have been investigated by single-crystal X-ray refinements of the structure. Sibirskite and parasibirskite are dimorphs of CaHBO3. Sibirskite at 295 K crystallizes in space group P121/c1 (no. 14), with a 3.5624(7), b 9.5225(19), c 8.6231(17) A, {beta} 119.452(3){degrees}, V 254.72(9) A3, and Z = 4. Parasibirskite at 295 K crystallizes in space group P121/m1 (no. 11), with a 6.6994(13), b 5.4269(11), c 3.5534(7) A, {beta} 93.048(11){degrees}, V 129.01(5) A3, and Z = 2. Priceite, (Ca2(H2O)[B5O7(OH)5]), at 173 K crystallizes in space group of P121/ c1 (no. 14), with a 11.580(3), b 6.9844(19), c 12.352(3) A, {beta} 110.573(9){degrees}, V 935.3(4) A3, and Z = 4. Our refinements allow determination of the positions of boron and hydrogen atoms in these minerals, which was not possible in previous powder XRD studies. In particular, the isolated [BO2(OH)] groups in sibirskite and parasibirskite are characterized by a long B-OH bond and two short B-O bonds, different from the [BO3] and [B(OH3)] groups in nesoborates. Periodic density functional theory (DFT) calculations for sibirskite and parasibirskite support those results of structure refinements and suggest that parasibirskite undergoes a displacive phase-transition involving hydrogen ordering below 173 K. Sibirskite and parasibirskite left in their parental solutions at ambient conditions decompose to form calcite.
    Print ISSN: 0008-4476
    Topics: Geosciences
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