Abstract

The crystal structures of four amphiboles from the Bear Lake diggings, in the Bancroft area of Ontario, fluorotremolite, fluororichterite and two samples of potassian fluor-magnesiokatophorite, have been refined to R indices in the range 1.5–2.2% using ~1380 unique reflections measured with Mo K α X-radiation. The crystals used in the collection of the X-ray intensity data were subsequently analyzed by electron and ion microprobes, and formulae were calculated using the Fe3+ and Fe2+ contents established by crystal-structure refinement. Site populations were assigned from the results of site-scattering refinement and stereochemical analysis, taking into account the unit formula determined for each crystal. Difference-Fourier maps through the A (2/ m ) site show that the A ( m ) site is occupied and the A (2) site is vacant in all crystals. Occupancy of the A ( m ) site, and not the A (2) site, by Na imposes strong constraints on the possible patterns of short-range order in these amphiboles. The site populations of the A ( m ), M (4) and O(3) sites are in accord with the local arrangement A ( m )(Na + K)–O(3)F– M (4)Na, with lesser amounts of A ( m )(Na + K)–O(3)OH– M (4)Na and major to minor amounts of A □–O(3)OH– M (4)Ca. The coupling of elements to specific short-range-ordered arrangements in these crystals suggests that the overall chemical variability of amphiboles is strongly constrained by local bond-valence restraints in addition to overall electroneutrality.

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