The Pingtan and Tonglu igneous complexes in SE China are typical of the calc-alkaline series developed at active continental margins. These two complexes are dominated by felsic rocks, temporally and spatially associated with minor mafic rocks. Morphological and trace-element studies of zircon populations in rocks from each of these complexes show that the zircon populations may be divided into 3–4 distinct growth stages, characterized by different distributions of morphological indices (Ipr, Ipy and Iel), and different contents of the substituting elements (Hf, U, Th, Y and P). The four growth stages recognized in the zircons are believed to have formed successively in the magma chamber, during the emplacement, and in the early and later stages of magma consolidation, respectively. All four stages are recognized in the plutonic Pingtan complex, whereas the stages 3 and 4 are less developed in the volcanic/subvolcanic Tonglu complex. Based on the chemistry and morphology of the different zircon populations of the Pingtan and Tonglu complexes, it is suggested that basaltic magmas underplating at the boundary between crust and mantle caused partial melting of the mid–lower crust and produced granitoid magmas. Subsequently, mixing between magmas was important.

Teruggite is the dominant phase in a soft, off-white, poorly-layered and weakly-cemented surface crust, 10–15 mm thick, occurring in the high-temperature El Tatio geothermal field of Chile. Other minerals present include halite, which is present throughout but also forms a thin (<0.5 mm), brittle, cratered surface to the deposit, nobleite, ulexite and opal-A, with possible traces of illite-smectite and at least one unidentified phase. With the exception of ulexite, none of the minerals associated with teruggite at El Tatio has been reported from other occurrences of this mineral, nor do they occur with nobleite in its sole other known occurrence in Death Valley. EDS and XPS analyses of the main mass of the deposit show the presence of Ca, As, B, Na, and Cl, consistent with the identified mineral assemblage, but with elevated concentrations in Ca and Cl that are presumably associated with a further phase. Little Mg is present and the El Tatio teruggite appears deficient in this element, with Ca presumably replacing Mg in the structure. Unlike earlier documented occurrences of teruggite, that at El Tatio is evaporitic, modern and surficial. It is located some 50 m from the nearest hot (~50°C) pool and there is no evidence of association with fluid discharge. As such, the deposit has presumably derived from a fluid moving in the uppermost levels of the El Tatio field; perhaps a heavily modified version of the brines found in the deep wells.

Sectored vesuvianite showing optically triclinic properties was studied by X-ray and P-FTIR analyses, and the origins of the internal optical texture are discussed. A monoclinic refinement (space group P2/n) suggests that site occupancies are slightly different among the Al(2) series, though the OH– dipole is randomly oriented in all sectors. A relationship between the surface and internal texture suggests that these sectoral structures were produced during crystal growth, not by phase transitions.

The origin of anomalous birefringence in grossular-andradite (grandite) garnets is considered. Using the point-dipole model we have calculated the anomalous optical indicatrix for four crystals (three from the paper by Takéuchi et al. (1982) and one studied previously by the present authors). The calculated indicatrix is in good agreement with the observed one. This suggests that the origin of anomalous birefringence in grandite garnets is due to Al/Fe ordering. Interrelations between the observed optical indicatrix, the structure of the growing face, the site occupancy in the crystal structure and the calculated optical indicatrix suggest a growth origin of Fe/Al ordering in grandite garnets and confirm the growth dissymmetrization hypothesis.

Electron microprobe analyses are presented of chevkinite-group minerals occurring as microphenocrysts in peralkaline rhyolites of the Greater Olkaria Volcanic Complex (Kenya) and as a groundmass phase in a peralkaline quartz trachyte lava from the Tarosero volcano (Tanzania), both in the East African Rift Valley. Their compositions conform closely to the formula: (REE, Ca, Th)4 Fe2+ (Fe2+, Al, Ti, Zr, Nb)2 Ti2 (Si4O22). Compared to published analyses of chevkinite-group minerals, the Olkaria phases are relatively enriched in Nb and the LREE; the Tarosero phase is more calcic and relatively Zr- and Nb-rich. The main substitution in the A site at Olkaria is Ca ⇌ Ce. The overall charge-balancing substitution seems to be (McDowell, 1979):

Phenocryst/glass ratios are presented for Nb, REE, Sr, Th, U and Y in two, and Ba, Zr and Hf in one, Kenyan samples. Partition coefficients are lower in the more peralkaline rock, with the exception of Sr, which is higher. The lower values are consistent with a lower degree of polymerization of more peralkaline melts. The higher Sr value may be a function of Sr partitioning into phenocryst phases coexisting with chevkinite.

Bobkingite, ideally is a new mineral from the New Cliffe Hill Quarry, Stantonunder-Bardon, Leicestershire, England. It occurs as very thin (⩽5 µm) transparent plates up to 0.2 mm across, perched on a compact fibrous crust of malachite and crystalline azurite attached to massive cuprite. Crystals are tabular on {001} with dominant {001} and minor {100} and {110}. Bobkingite is a soft pale blue colour with a pale-blue streak, vitreous lustre and no observable fluorescence under ultraviolet light. It has perfect {001} and fair {100} cleavages, no observable parting, conchoidal fracture, and is brittle. Its Mohs' hardness is 3 and the calculated density is 3.254 g/cm3. Bobkingite is biaxial negative with α = 1.724(2), β = 1.745(2), γ = 1.750(2), 2Vγmeas = 33(6)°, 2Vcalc = 52°, pleochroism distinct, X = very pale blue, Z = pale greenish blue, X^a = 22° (in β obtuse), Y = c, Z = b. Bobkingite is monoclinic, space group C2/m, unit-cell parameters (refined from powder data): a = 10.301(8), b = 6.758(3), c = 8.835(7)Å, β = 111.53(6)°, V = 572.1(7)Å3, Z = 2. The seven strongest lines in the X-ray powder-diffraction pattern are [d (Å), I, (hkl)]: 8.199, 100, (001); 5.502, 100, (110); 5.029, 40, (01); 2.883, 80, (310); 2.693, 40, (13); 2.263, 40, (113), (03); 2.188, 50, (23). Chemical analysis by electron microprobe and crystal-structure solution and refinement gave CuO 70.46, Cl 12.71, H2O 19.19, O≡Cl –2.87, sum 99.49 wt.%, where the amount of H2O was determined by crystal-structure analysis. The resulting empirical formula on the basis of 12 anions (including 8 (OH) and 2H2O) is Cu4.99Cl2.02O10H12. The crystal structure was solved by direct methods and refined to an R index of 2.6% for 638 observed reflections measured with X-rays on a single crystal. Three distinct (Cuϕ6) (ϕ = unspecified anion) octahedra share edges to form a framework that is related to the structures of paratacamite and the Cu2(OH)3Cl polymorphs, atacamite and clinoatacamite. The mineral is named for Robert King, formerly of the Department of Geology, Leicester University, prominent mineral collector and founding member of the Russell Society. The mineral and its name have been approved by the Commission on New Minerals and Mineral Names of the International Mineralogical Association.

In most documented occurrences, violarite (FeNi2S4) occurs as a product of the supergene alteration of primary pentlandite or millerite. Earlier experimental phase relations studies predicted the possible existence of a stable violarite–pentlandite tie line, though there has been little field evidence supporting this hypothesis, and the preferred topology in the Ni-Fe-S system involves a pyrite–millerite tie line. This paper documents the occurrence of violarite-pentlandite±pyrite assemblages which, on the basis of mineral chemistry and textural evidence, appear to be hypogene. Primary cobaltian violarite (with 2.1–13.2 wt.% Co) occurs as lamellae in pentlandite in the MKD5 nickel sulphide orebody at Mount Keith, central Western Australia. These lamellae are interpreted to be of exsolution origin. Cobalt is preferentially partitioned into violarite, resulting in high Ni:Co ratios in the associated pentlandite relative to pentlandite in violarite-free assemblages. Hypogene violarite-millerite±pentlandite assemblages were also noted. In all hypogene assemblages, violarite differs in both textural and mineral chemical characteristics from supergene violarite from the upper portions of the MKD5 orebody. The implications of the assemblages for the known low-temperature phase relations in the Ni-Fe-S-(Co) system are discussed.

Palladseite (palladium selenide) and palladian gold occur as euhedral inclusions in specularite and as infill of microfractures and interstices in magnetite aggregates (host rock fragments) within specularite-rich auriferous veins (jacutinga). Palladseite has minor amounts of Pt (0.6–3.5 wt.%), Cu (2.9–3.5 wt.%), Hg (0.9–1.9 wt.%), and Ag (0.3–0.5 wt.%). The palladian gold contains up to 6 wt.% Pd, and minor Cu and Ag. Isomertieite (Pd11Sb2As2) and sudovikovite (PtSe2) are also recorded. The veins cross-cut the main tectonic foliation of the wallrock (itabirite). The feature of fracture infill and the Se-Sb-As-Hg-Cu-Ag geochemical/mineralogical signature of the Au-Pd mineralization point to a post-ductile deformation and possibly low-temperature (epithermal) origin of the jacutinga mineralization style.

Palladseite is replaced locally by a Pd-rich oxidation phase. Electron microprobe analysis of alteration halos around palladseite yields 76–80 wt.% Pd. Oxygen calculated by stoichiometry accords with a monoxide compound of the type PdO. However, the measured oxygen content is lower than expected for the PdO stoichiometry, suggesting loss of volatile species, and a more ‘hydrated’ compound, such as an oxyhydroxide.

The first recorded occurrence of cummingtonite in the Scottish Dalradian is described. The mineral occurs in thin layers within a psammite-semipelite sequence forming the lower part of the Easdale Subgroup in which it coexists with bytownitic plagioclase, almandine-rich garnet and quartz. Textural and mineral chemical evidence suggest that the cummingtonite developed from hornblende during amphibolite-facies regional metamorphism. The protolith to this cummingtonite-bearing rock is believed to have been a basaltic tuff, possibly alkaline in character, containing a significant proportion of sedimentary detritus. The cummingtonite-bearing rock may provide the earliest record of basic volcanism in the Dalradian of the Ballater district.

A new occurrence of barysilite, Pb8Mn(Si2O7)3, at the polymetallic Garpenberg Norra Zn-Pb deposit, Hedemora, Dalarna, Sweden, is described. The mineral, which forms colourless, transparent grains, is characterized by X-ray diffraction and electron-microprobe analyses. The assemblage includes tephroite, zincian jacobsite, manganoan diopside and others. The crystal structure of a barysilite crystal from Garpenberg Norra was redetermined using single-crystal X-ray diffraction data (Mo-Kα, CCD area detector) and has been refined in space group Rc with a = 9.804(1), c = 38.416(8)Å, V = 3197.8(8)Å3, to R1 = 2.32% for 1025 ‘observed’ reflections with Fo >4σ(Fo). A previous, low-precision structure determination (Lajzérowicz, 1965; R = 20%) is confirmed but improved considerably. The structure contains one distorted MnO6 polyhedron with six equivalent Mn–O bonds (2.224 Å), one Si2O7 disilicate unit with an Si–O–Si angle of 120.9°, and two non-equivalent Pb sites. The Pb1 site has a highly irregular, one-sided coordination with six O ligands, indicating a stereoactive 6s2 lone-electron pair on the Pb2+ ion, whereas the [6+3]-coordinated Pb2 site is fairly regular, with Pb–O distances of 2.540 (3×), 2.674 (3×) and 3.098 (3×) Å. The Pb2 site contains ~10% of Ca (+Ba) replacing Pb, corresponding to the structural formula Pb16(Pb,Ca)22Mn(Si2O7)3. This is the first direct proof that not only the M site in barysilite-type Pb8M(Si2O7)3 compounds can be replaced by divalent cations.