Abstract
Due to its strong chalcophile character and the influence of its s2 lone-pair electrons on the crystal structure trivalent bismuth is extremely rare in silicate minerals, with Bi-contents in common silicates typically below 1 ppm. In the present paper, we report on an exceptionally Bi-rich variety of the rock-forming mineral vesuvianite with up to ca. 20 wt% Bi2O3, occasionally in combination with enhanced Pb contents up to ca. 5 wt% PbO. The mineral occurs as small (≤300 μm) idiomorphic, black crystals in a sulfide-free silicate skarn in the Långban Mn-Fe deposit, central Sweden. The major skarn minerals comprise Ba-rich potassium feldspar, albitic plagioclase, Pb-rich scapolite, and phlogopite, while Pb-rich epidote, vesuvianite, and calcic garnets are minor phases. The vesuvianite grains are intensely zoned displaying Bi-rich cores surrounded by thinner Bi-poor rims. Although generally high in bismuth, the crystal cores invariably show oscillatory zoning. In addition to high Bi- and Pb-contents, the crystals are occasionally enriched in copper, cerium, antimony, and arsenic, thus reflecting the complex chemistry and evolution of the Långban mineralization.
Chemical analyses demonstrate a strong negative correlation between Ca and Bi, hence confirming that Bi replaces Ca at X sites of the vesuvianite structure. Concentrations of Si and Al are lower, while Fe and Ti contents are somewhat enhanced in the Bi-rich cores. Maximum Bi and Pb contents analyzed in the present vesuvianite crystals correspond to 3.19 and 0.87 atoms per formula unit, respectively. This exceeds by far previous reports in the literature. X-ray single-crystal diffraction studies of a crystal splinter with intermediate Bi-content (1.08 apfu) show that the space group P4/nnc is the most appropriate to describe the crystal structure; the refinement converged to an R1 index of 0.0493. The recorded unit-cell parameters, a = 15.7018(6), c = 11.8648(6) Å, and V = 2925.2(2) Å3, are to our knowledge the largest ones observed so far for P4/nnc vesuvianite. Bismuth was demonstrated to order at the X3′(Bi) site that is only 0.46 Å distant from the nearest X3(Ca) site. Consequently, the X3 and X3′ sites cannot be simultaneously fully occupied.
© 2015 by Walter de Gruyter Berlin/Boston
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- Static disorders of atoms and experimental determination of Debye temperature in pyrope: Low- and high-temperature single-crystal X-ray diffraction study—Reply
Articles in the same Issue
- Highlight and Breakthrough. A fresh look at crystals in the Bishop Tuff
- Actinides in Geology, Energy, and the Environment. Remobilization of U and REE and the formation of secondary minerals in oxidized U deposits
- Actinides in Geology, Energy, and the Environment. Revision of the symmetry and the crystal structure of čejkaite, Na4(UO2)(CO3)3
- Characterization of ferric arsenate-sulfate compounds: Implications for arsenic control in refractory gold processing residues
- Crystal structure and chemistry of skarn-associated bismuthian vesuvianite
- Transformation of graphite to lonsdaleite and diamond in the Goalpara ureilite directly observed by TEM
- Quartz nanocrystals in the 2.48 Ga Dales Gorge banded iron formation of Hamersley, Western Australia: Evidence for a change from submarine to subaerial volcanism at the end of the Archean
- Synthesis and characterization of amphiboles along the tremolite–glaucophane join
- Elasticity of franklinite and trends for transition-metal oxide spinels
- Redox systematics of martian magmas with implications for magnetite stability
- Hydrogen incorporation and the oxidation state of iron in ringwoodite: A spectroscopic study
- Hydrous ringwoodite to 5 K and 35 GPa: Multiple hydrogen bonding sites resolved with FTIR spectroscopy
- Calibration of zircon as a Raman spectroscopic pressure sensor to high temperatures and application to water-silicate melt systems
- Computational study of the elastic behavior of the 2M1 muscovite-paragonite series
- Vanadium L2,3 XANES experiments and first-principles multielectron calculations: Impact of second-nearest neighboring cations on vanadium-bearing fresnoites
- A time-resolved X-ray diffraction study of Cs exchange into hexagonal H-birnessite
- Grain-boundary diffusion rates inferred from grain-size variations of quartz in metacherts from a contact aureole
- On the use of unpolarized infrared spectroscopy for quantitative analysis of absorbing species in birefringent crystals
- A computational model of cation ordering in the magnesioferrite-qandilite (MgFe2O4- Mg2TiO4) solid solution and its potential application to titanomagnetite (Fe3O4-Fe2TiO4)
- 3T-phlogopite from Kasenyi kamafugite (SW Uganda): EPMA, XPS, FTIR, and SCXRD study
- Revision of the crystal structure and chemical formula of haiweeite, Ca(UO2)2(Si5O12)(OH)2·6H2O
- Cation arrangement in the octahedral and tetrahedral sheets of cis-vacant polymorph of dioctahedral 2:1 phyllosilicates by quantum mechanical calculations
- High-pressure phase transitions of Fe3–xTixO4 solid solution up to 60 GPa correlated with electronic spin transition
- Hydrogen incorporation in crystalline zircon: Insight from ab initio calculations
- The vibrational features of hydroxylapatite and type A carbonated apatite: A first principle contribution
- STEM investigation of exsolution lamellae and “c” reflections in Ca-rich dolomite from the Platteville Formation, western Wisconsin
- Karenwebberite, Na(Fe2+,Mn2+)PO4, a new member of the triphylite group from the Malpensata pegmatite, Lecco Province, Italy
- The crystal structure of ramdohrite, Pb5.9Fe0.1Mn0.1In0.1Cd0.2Ag2.8Sb10.8S24: A new refinement
- Static disorders of atoms and experimental determination of Debye temperature in pyrope: Low- and high-temperature single-crystal X-ray diffraction study—Discussion
- Static disorders of atoms and experimental determination of Debye temperature in pyrope: Low- and high-temperature single-crystal X-ray diffraction study—Reply