Sugilite relatively rich in manganese has been found at two new localities, the Hoskins and Woods mines in New South Wales, Australia. The occurrences are in manganese-rich silicate rocks of middle to upper greenschist facies (Hoskins mine) and hornblende hornfels facies (Woods mine). Coexisting minerals are members of the namansilite-aegirine and pectolite-serandite series, Mn-rich alkali amphiboles, alkali feldspar, braunite, rhodonite, tephroite, albite, microcline, norrishite, witherite, manganoan calcite, quartz, and several unidentified minerals. Woods mine sugilite is colour-zoned with pale mauve cores and colourless rims, whereas Hoskins mine sugilite is only weakly colour-zoned and pink to mauve. Within single samples, the chemical compositions of sugilite from both localities show wide ranges in Al contents and less variable ranges of Fe and Mn, similar to trends in sugilite from other localities. The refractive indices and cell dimensions tend to show systematic increases progressing from Al-rich to Fe-Mn-rich. The formation of the sugilite is controlled by the high alkali (especially Li) and manganese contents of the country rock, reflected in the occurrences of coexisting high alkali- and manganese-bearing minerals, and by high fo2 conditions.

Members of the roedderite-chayesite series in lamproites from Cancarix (SE Spain), crystallized from late magmatic residua under low PH2O, high temperature (∼ 1100°C), oxidizing conditions. They exhibit the following main chemical variations: 0.14 ⩽ Na ⩽ 0.62 atoms per formula unit (apfu); 0.80 ⩽ K⩽ 1.00 apfu; 2.97 ⩽ Mg ⩽ 4.33 apfu; 0.00 ⩽ Fe2+ ⩽ 1.19 apfu; 0.42 ⩽ Fe3+ ⩽ 0.87 apfu; they are hexagonal (10.120 ⩽ a ⩽ 10.135 Å, 14.305 ⩽ c ⩽ 14.326 Å), P6/mcc. The characteristic chemical substitution is: Fe3+ + □ ⇌ Fe2+ + (K+Na)+. Six crystal structures have been refined to 0.020 ⩽ Robs ⩽ 0.026. They have the osumilite/milarite-type structure, with Si entering the double tetrahedral T1 six-membered rings, and Mg and Fe entering both the ring-linking T2 tetrahedra, and the A octahedra. The 12-coordinated C site, located between two double rings of T1 tetrahedra, is occupied mainly by K and subordinately by Na. Furthermore, Na occupies the partially empty nine-fold coordinated B site which occurs both in the ideal (z = 0) and in a split-atom position along the c direction.

Berezanskite, ideally Ti□2KLi3(Si12O30), is hexagonal, space group P6/mcc, a = 9.898(4), c = 14.276(6) Å, V = 1211.2(9) Å3, Z = 2. The crystal structure was refined to an R1 index of 2.08% based on 392 unique observed reflections. Berezanskite is isostructural with milarite, ideally ACa2BoCKT(2)(Be2Al)(T(1)Si12O30)(H2O)0–2. The structural unit is of the form [T(2)3T(1)12O30] with T(1) = Si and T(2) = Li, in which (LiO4) tetrahedra link [Si12O30] six-membered double-rings into a framework. The A, B and C sites occur in the interstices of the framework with the following site populations: A = Ti4+2, <A–O>= 1.938(2) Å; B =□2; C = K, <C–O> = 3.058(2) Å. In the T(2) = Li3 milarite-group minerals, the <C–O> distance is inversely related to the occupancy of the B site.