학술논문

Single-crystal X-ray studies of trioctahedral micas coexisting with dioctahedral micas in metamorphic sequences from western Maine
Document Type
research-article
Source
American Mineralogist. 93(2-3):396-408
Subject
Biotite
muscovite
western Maine
crystal chemistry
crystal structure
Language
English
ISSN
1945-3027
0003-004X
Abstract
A crystal-chemical study of thirteen biotite (twelve of 1M polytype and one of 2M1 polytype) and four muscovite samples was made. The biotite coexists with the muscovite. Samples are from metamorphic terranes and from granitic and granodioritic bodies occurring in three areas of western Maine. The metamorphic mineral zones identified by mineral compatibilities are, in order of increasing metamorphic grade: the Lower Sillimanite Zone (LSZ), the Upper Sillimanite Zone (USZ), and the K-feldspar + Sillimanite Zone (K + SZ).The muscovite compositions cluster near ideal muscovite and display a small celadonite substitution and a small, but variable, paragonite substitution. The biotite composition has values of VIMg2+/ VI(Mg2+ + Fe2+) ranging from 0.26 to 0.54 and significant octahedral Al content (0.48 ≤ VIAl ≤ 0.72 apfu in metamorphic biotite samples, 0.51 ≤ VIAl ≤ 0.67 in those from granites).In trioctahedral micas from western Maine and especially in those with graphite, there are a greater number of interlayer vacancies than in common micas. Interlayer vacancies have an increase in interlayer cation-basal oxygen atom distances and a decrease in tetrahedral flattening angle τ, thus suggesting a reduced interlayer charge. With a few exceptions, tetrahedral rotation angle α is related to crystallization temperature. In particular, α decreases with a temperature increase, and α is also related to octahedral chemical substitutions. Results tentatively suggest, for micas from metamorphic environments, a direct influence of genetic parameters (T and fO₂) on mica crystal structure, and not just chemical composition.