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Dissymmetrization in tourmaline: the atomic arrangement of sectorally zoned triclinic Ni-bearing dravite

Hughes, John M. and Rakovan, John and Ertl, Andreas and Rossman, George R. and Baksheev, Ivan and Bernhardt, Heinz-Jürgen (2011) Dissymmetrization in tourmaline: the atomic arrangement of sectorally zoned triclinic Ni-bearing dravite. Canadian Mineralogist, 49 (1). pp. 29-40. ISSN 0008-4476. https://resolver.caltech.edu/CaltechAUTHORS:20110401-112705034

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Abstract

Although putatively possessing hexagonal R3m symmetry, reports of optically anomalous tourmaline are common, and recently an occurrence of triclinic tourmaline was reported with dissymmetrization that resulted from non-equivalency of the occupants of the Y sites. We report the atomic arrangement of Ni-bearing dravite from the Berezovskoe gold deposit, Middle Urals, Russia, in the non-conventional triclinic space-group R1 (R = 4.41%) to facilitate comparison with the conventional tourmaline R3m cell. The dissymmetrization occurs as a result of inequalities among both the hexagonally equivalent Y and hexagonally equivalent Z tourmaline sites. The atomic arrangement of this triclinic dravite demonstrates that the atomic arrangement of tourmaline is robust, and is capable of incorporating various substituents by modifying the putative hexagonal structure in lower symmetries, suggesting that further exploration of tourmaline’s role in trace-element variation is warranted. Optical studies demonstrate the heterogeneous biaxial character of the crystals. Domains of different optical orientation and 2V correspond directly to trigonal prism |100|, |010| and pedion |001| sectors, indicating optical sectoral zoning. Compositional sectoral and concentric zoning are also observed within the crystals. Spectroscopic studies show the optical absorption spectrum of the Berezovskoe tourmaline has strong absorptions in the 400, 600–700, and 1100 nm regions, in addition to OH features near 1450, 2300, and 2700 nm. We conclude that the color in the E ⊥ c polarization comes dominantly from Fe mixed-oxidation-state couples on the Y sites, and from Cr^(3+). Contributions to the color from the nickel are believed to be minor and will fall in the regions of strong Cr and Fe absorption. The ordered arrangement of cations on the Y and Z sites and the correlation of optical orientation with specific sectors indicate that dissymmetrization occurs during growth by differential incorporation at structurally different atomic sites at the surface of the crystal, which in the bulk are symmetrically equivalent.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.3749/canmin.49.1.29DOIUNSPECIFIED
http://www.canmin.org/cgi/content/abstract/49/1/29PublisherUNSPECIFIED
ORCID:
AuthorORCID
Rossman, George R.0000-0002-4571-6884
Additional Information:© 2011 Mineralogical Association of Canada. Received November 19, 2009; revised manuscript accepted January 9, 2011. This work was supported in part by National Science Foundation (U.S.A) grants EAR–0003201 to JMH and EAR–0337816 to GRR. Darrell Henry and an anonymous reviewer provided insightful and valuable comments on the work, and Editor-in-Chief Robert F. Martin provided his typical outstanding review; sincere thanks to all. This work was supported in part by Österreichischer Fonds zur Förderung der wissenschaftlichen Forschung (FWF) project no. P20509–N10.
Funders:
Funding AgencyGrant Number
NSFEAR-0003201
NSFEAR-0337816
Österreichischer Fonds zur Förderung der wissenschaftlichen Forschung (FWF)P20509-N10
Subject Keywords:tourmaline; optical sectoral zoning; dissymmetrization; triclinic; optical anomaly; dravite; Berezovskoe gold deposit; Russia
Issue or Number:1
Record Number:CaltechAUTHORS:20110401-112705034
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20110401-112705034
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:23204
Collection:CaltechAUTHORS
Deposited By: Jason Perez
Deposited On:19 Apr 2011 18:00
Last Modified:03 Oct 2019 02:44

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