Wupatkiite (Co,Mg,Ni)Al2(SO4)4.22H2O is a new member of the halotrichite group. It occurs 8 miles ESE of Gray Mountain, Arizona, near the prehistoric pueblo dwelling Wupatki. It occurs as cross-fibre veinlets with fibres up to 8mm long. Colour: empire rose (RHS48C), streak white, H. = 1 ½. G = 1.92, D(calc) = 1.87g/cm3. Nonpleochroic with α = 1.477, γ = 1.484, Z^fibre axis = 12°. Wet chemistry gave MgO 1.63, CaO 0.10, MnO 0.17, FeO 0.15, NiO 0.52, CuO 0.12, CoO 3.41, Al2O3 11.30, SO3 35.97, H2O 42.26 (total 95.63%); rem. = montmorillonite and quartz. Parameters refinedo from the powder pattern are close to those of halotrichite. Wupatkiite is monoclinic P21/c with a = 6.189 Å, b = 24.23 Å, c = 21.20 Å, β = 100.33°. Strongest lines are 4.790, 100 (024); 4.295, 27 (140); 3.945, 26 (025); 3.768, 33 (062); 3.494, 92 (124, 063).

The crystal structure of vlodavetsite, AlCa2(SO4)2F2Cl·4H2O, has been determined, space group I4/m, a = 6.870(1), c = 13.342(2) Å, Z = 2, Dx = 2.35 g/cm3. The polyhedron cation chains are parallel to [001] and consist of couples of distorted Ca octahedra alternating with one distorted Al octahedron rotated through 24° with respect to the former. The chains are linked by SO4-tetrahedra so that all of the four tetrahedron oxygen atoms take part in coordination of Ca atoms to form a distorted octahedron with Cl and F atoms. The Al coordination polyhedron consists of two F atoms and four oxygen atoms belonging to water molecules. There is a specific interaction via hydrogen bonds between oxygen atoms of SO4-tetrahedra and water molecules.

Petrological and mineral chemical data are presented for two new occurrences of co-existing borosilicate minerals in the Larsemann Hills, East Antarctica. The assemblages contain kornerupine and the rare borosilicate, grandidierite (Mg,Fe)A13BSiO9. Two distinct associations occur: (1) At McCarthy Point, 1–10 mm thick tourmaline-kornerupine-grandidierite layers are hosted within quartzofeldspathic gneiss; and (2) Seal Cove, where coexisting kornerupine and grandidierite occur within coarse-grained, metamorphic segregations with Mg-rich cores of cordierite-garnet-spinel-biotite-ilmenite and variably developed plagioclase halos. The segregations are hosted within biotite-bearing, plagio-feldspathic gneiss. Textural relationships from these localities indicate the stability of co-existing kornerupine and grandidierite.

The grandidierite- and kornerupine-bearing segregations from Seal Cove largely postdate structures developed during a crustal thickening event (D2) which was coeval with peak metamorphism. At McCarthy Point, grandidierite, kornerupine and late-tourmaline growth predates, or is synchronous, with F3 fold structures developed during a extensive granulite grade, normal shearing event (D3) which occurred prior to, and synchronous with, near-isothermal decompression. Average pressure calculations on assemblages that coexist with the borosilicates at Seal Cove, indicate the prevailing conditions were 5.2–5.5 kbar at ∼ 750°C for formation of the grandidierite-kornerupine assemblage.

Penfieldite is a lead hydroxychloride mineral with composition Pb2Cl3(OH). It belongs to the hexagonal system, space group P, a = 11.393(3), c = 4.024(1) Å. The 4 Å c parameter corresponds to the basic sub-cell, whereas modulated structures are known with a true c axis 12 times longer. The average crystal structure of penfieldite has been solved with direct methods and refined to Rw = 0.041 for 871 refections collected with Mo-Kα radiation. The chemical and structural relationships between penfeldite and laurelite, Pb2F3(F,Cl,OH), are briefly discussed. An electron diffraction study of penfieldite revealed the occurrence, besides the common modulated structure with C = 12c, of domains with a 15c periodicity. Moreover, a 9c periodicity has been observed in crystals heated at 180°C Penfieldite is quickly destroyed above 200°C.