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Mn-tourmaline from island of Elba (Italy): Crystal chemistry

  • Ferdinando Bosi EMAIL logo , Giovanna Agrosì , Sergio Lucchesi , Giovanni Melchiorre and Eugenio Scandale
Published/Copyright: March 28, 2015
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Abstract

The crystal chemistry of seven crystal fragments taken from differing regions of the same colorless to yellow-greenish tourmaline macro-crystal from pegmatite pockets in aplite veins (island of Elba, Italy) was studied with a multi-disciplinary (SREF, XRDT) and multi-analytical approach (EMPA, SIMS). EMPA and XRDT studies showed relationships between color and chemical zoning and crystal- growth evolution, indicating which fragments could be considered representative of the chemical evolution of the genetic micro-environment in which the crystal developed. Results showed that the colorless fragment is an elbaite while the yellow-greenish crystal fragments are Mn2+-rich (up to 1.34 apfu) and belong to the alkali group and fluor subgroup. They are characterized by dehydroxylation and alkali-defect type substitutions that cooperate in reducing Li and increasing Mn contents. The Y site is populated by Al, Li, and Mn2+, and the Z site by Al and Mn2+ (up to 0.10 apfu). In contrast with data in the literature, Mn2+ populates both octahedral sites according to the order-disorder reaction: YMn + ZAl ↔ YAl + ZMn. As Mn2+ content increases, progressive disorder takes place. This disorder is quantitatively lower than that of the ZMg in dravite, due to the low structural tolerance of the small Z cavity in the incorporation of larger cations by the ZR2+ZAl substitution. Relationships of direct proportionality between lattice parameters and both <Y-O> and <Z-O> are observed. The expansion of both octahedra, as well as of lattice parameters, increases linearly as a function of YMn2+ and ZMn2+. The latter has greater weight in dictating unit-cell variations, due to the degree of size mismatch between ZMn2+ZAl and YMn2+YLi substitutions, and the way in which the Z octahedra are articulated in the structure.

Received: 2004-11-18
Accepted: 2005-2-11
Published Online: 2015-3-28
Published in Print: 2005-10-1

© 2015 by Walter de Gruyter Berlin/Boston

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