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Coexistence of Two Polytypic Groups in Cronstedtite From Lostwithiel, England

Published online by Cambridge University Press:  01 January 2024

Toshihiro Kogure*
Affiliation:
Department of Earth and Planetary Science, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan
Jiří Hybler
Affiliation:
Institute of Physics, Science Academy of the Czech Republic, Na Slovance 2, CZ-18221, Praha 8, Czech Republic
Hideto Yoshida
Affiliation:
Department of Earth and Planetary Science, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan
*
*E-mail address of corresponding author: kogure@eps.s.u-tokyo.ac.jp

Abstract

Cronstedtite from Lostwithiel, Cornwall, England, in which two polytypic groups (A and C) are present within the same crystal, has been investigated using various techniques to reveal the distribution of the two groups and the relationship between polytypic structure and chemical composition. X-ray precession photographs from cleaved fragments of pyramidal crystals revealed the variable proportions of the two groups from the top to the base. Near the top, the crystal consists entirely of group C, with 1T as the dominant polytype. Near the base, both groups A and C are present. Back-scattered electron images from cross-sections parallel to the pyramidal axis showed mosaic contrast near the base, suggesting that two compositionally-different domains of several tens of microns in size are present, whereas the contrast was uniform near the top. Electron microprobe chemical analysis indicated the compositions (Fe2.312+Fe0.693+)(Si1.31Fe0.693+)O5(OH)4 and (Fe2.162+Fe0.843+)(Si1.16Fe0.843+)O5(OH)4. Electron back-scattered patterns (EBSPs) confirmed that the domain with Si-rich composition belongs to group C and that with Si-poor composition to group A. This is the first evidence that specific chemical compositions are related to the polytypic structures in cronstedtite. Transmission electron microscopy revealed that intergrowth of groups A and C at the monolayer level is also present as stacking disorder in both domains near the base, whereas such intergrowth was not observed in the region near the top.

Type
Research Article
Copyright
Copyright © 2002, The Clay Minerals Society

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