Long-range ordering of tetrahedral cations in micas is favored by phengitic compositions, by the 3T stacking sequence of layers, and by tetrahedral Si:Al ratios near 1:1. Phengites of the 1M, 2M1, and 2M2 polytypes are said to show partial ordering of tetrahedral cations, although the amounts of tetrahedral substitutions are small and the accuracies of determination are not as large as desired. The 3T structures of muscovite, paragonite, lepidolite, and protolithionite show tetrahedral ordering, as do the 2M1 brittle micas margarite and an intermediate between margarite and bityite. Muscovite-3T and margarite-2M1 are also slightly phengitic relative to their ideal compositions. Examples of octahedral cation ordering in micas are more abundant and are to be expected when cations of different size and charge are present. Octahedron M(1) with its OH,F groups in the trans orientation tends to be larger than the mean of the two cis octahedra as a result of the ordering of cations and vacancies. In some samples ordering has reduced the true symmetry to a subgroup of that of the ideal space group. If ordering in subgroup symmetry results in ordered patterns of different geometries but similar energies in very small domains, the average over all unit cells may simulate long-range disorder.

Rectorites containing various amounts of Ca were found at the Sano Mine, Nagano Prefecture, Japan. The Ca content in nonexchangeable form varied from 1.0 to 3.9% CaO. With more than 3.4%, they may be called Ca-rectorite. Chemical data of the most Ca-rich sample showed that Ca was the dominant interlayer cation, and gave a structural formula of (Mg0.16)EX(Ca0.59Na0.27K0.17)FIX[Al3.94Mg0.08 Fe0.07Ti0.01](Si5.85Al2.15)O20(OH)4. This sample is apparently the most Ca-rich rectorite reported to date. The Greene-Kelly test and an intercalation examination by octadecylammonium indicated that the expandable component layers were beidellitic. Assuming the tetrahedral composition of the expandable component layers are similar to the average tetrahedral composition of beidellite of (Si3.6Al0.4), the tetrahedral composition of the mica-like component layers was calculated to be (Si2.25Al1.75). This was closer to a brittle mica (margarite) than to a true mica. Examination of chemical data for several Ca-rectorite samples from different localities, including those from the Sano Mine, showed a trend of increasing Ca content as Al increased and Si decreased. Ca-rectorite exhibited characteristic infrared absorption bands at 480, 670–700 and 900–930 cm−1, which became more intense as Ca content increased. These bands also corresponded to major absorption bands of margarite.

Triassic sequences from 'intermediate units' between the Alpujárride and the Malâguide complexes (Betic Cordilleras, Spain) of the westernmost part of the Cordilleras (Casares area) occur as four superimposed tectonic units; the uppermost unit shows lithological characteristics similar to those of the Malâguide complex, changing progressively at increasing depth, towards lithologies typical of the Alpujárride complex. The units studied, with a maximum thickness of ~400 m, record important variations in metamorphic pressures, according to the b parameter of white micas: from low-pressure metamorphism (in the unper unit) to high-pressure faciès series (in the deepest one). The mean b values range from 8.988 Å in the uppermost unit (Crestellina) to 9.042 Å in the lowermost one (Jubrique). The lowest metamorphic grade is represented by mineral assemblages consisting of phengite + intermediate Na-K white mica ± Fe-chlorite ± sudoite ± pyrophyllite, which record temperatures of ~300°C and pressures of 1.5—3 kbar. At increasing tectonic depth, intermediate Na-K mica and pyrophyllite disappear and the metamorphic assemblages consist of phengite ± paragonite ± margarite + Mg-chlorite ± sudoite, which record minimum pressures of ~7 kbar and temperatures in the order of 400—450°C. These mineral assemblages provide evidence of the passage from collisional to extensional geotectonic settings. The units showing different metamorphic patterns were juxtaposed tectonically, after the development of metamorphic mineral assemblages.

We report an unusual occurrence of margarite, corundum, gahnite and zincohögbomite from the Raleigh terrane in the Piedmont Province of Virginia. The assemblage occurs in a chlorite-rich blackwall associated with a small metamorphosed ultramafic rock body. The blackwall is dominated by chlorite, but also contains distinctive clusters (1–4 mm across) that typically consist of ragged Zn-rich spinel grains surrounded by masses of randomly oriented margarite. Also spatially associated with spinel are smaller grains of corundum and högbomite. In most cases, spinel and högbomite are sufficiently enriched in Zn to be called gahnite and zincohögbomite, respectively. Some högbomite grains are distinctly banded in back-scattered electron images, primarily reflecting variations in Zn-content. Textures suggest that högbomite formed at the expense of spinel (although locally the reverse relationship holds), and högbomite compositions mimic those of spinel. Margarite appears to be a later phase, and textures imply formation via reactions with spinel, corundum and, possibly, chlorite. This occurrence of Zn-rich spinel and högbomite is clearly related to the bulk composition of the blackwall rock, which contains >2500 ppm Zn. The origin of this Zn-rich composition is unclear, but could be due to a small amount of sphalerite or zincian-staurolite in the protolith.