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Licensed Unlicensed Requires Authentication Published by De Gruyter April 9, 2015

Balestraite, KLi2VSi4O10O2, the first member of the mica group with octahedral V5+

  • Giovanni O. Lepore , Luca Bindi , Alberto Zanetti , Marco E. Ciriotti , Olaf Medenbach and Paola Bonazzi EMAIL logo
From the journal American Mineralogist

Abstract

A mica-group mineral characterized by a high V content and free of Al was found in the mangane- siferous beds within the metacherts of the ophiolitic sequences at the Cerchiara mine, Eastern Liguria (Italy), in association with hematite, quartz, and calcite. Chemical and structural characterization supported by Raman data defines this phase as a new mineral species, which is named balestraite after Corrado Balestra, a prominent Italian amateur mineralogist. Balestraite, ideally KLi2V5+Si4O10O2, is a 1M trioctahedral mica crystallizing in the C2 space group, with a = 5.2024(5), b = 8.9782(7), c = 9.997(2) Å, β = 100.40(2)°, V = 459.3(1) Å3, Z = 2. The reduction of symmetry from the “ideal” space group C2/m is related to the ordering of V at only one of the two pseudo-symmetric octahedral sites. Vanadium forms very distorted octahedra with a [2+2+2] geometry characteristic of the valence state +5. The Li,V composition of the octahedral sheet, the pure tetrasilicic character of the tetrahedral sheet, and the anhydrous character produce unusual geometrical features for this mica. The occurrence of 5+ as the dominant valence state of V and the virtually complete O2- → OH- substitution at the O4 site indicate strongly oxidizing conditions of crystallization, which are consistent with balestraite occurring at the boundary between carbonate-bearing veins and hematite bands. The new mineral and name were approved by the Commission on New Minerals, Nomenclature and Classification, IMA (2013-080).

Received: 2014-3-12
Accepted: 2014-8-31
Published Online: 2015-4-9
Published in Print: 2015-2-1

© 2015 by Walter de Gruyter Berlin/Boston

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