Schäferite, NaCa2Mg2(V5+O4)3; palenzonaite, NaCa2Mn22+(V5+O4)3; berzeliite, NaCa2Mg2(As5+O4)3; and manganberzeliite, NaCa2Mn2+2(As5+O4)3, are cubic minerals with garnet structures (space group Iad) in which tetrahedrally coordinated V5+ and/or As5+ at the Z site are charge balanced by disordered Na+ and Ca2+ at the X site, and divalent Mg2+ and Mn2+ cations at the octahedrally coordinated Y site. The crystal chemistry of palenzonaite (from the Molinello and Gambatesa mines, Italy, and the Fianel mine, Switzerland), berzeliite (from Långban, Sweden, and Montaldo, Italy), and manganberzeliite (from Varenche, Italy, and the Gozaisho mine, Japan) were studied by electron microprobe analysis and single-crystal X-ray diffraction methods. Structure refinements converged to R1 values of 1.36–2.42%. The tetrahedral site in these garnet structures is mainly occupied by pentavalent As5+ or V5+ (only up to about 20% randomly distributed Si4+ is present). Charge balance is maintained by variations in the Ca/Na ratio at the X site. Heterovalent substitution (Na+ ↔ Ca2+) at the distorted square antiprism X site in vanadate- and arsenate-bearing garnets allows full occupancy of the octahedral Y site by divalent cations (primarily Mg2+ and Mn2+). There is a positive correlation between the <Z–O> and <Y–O> bond lengths and the mean ionic radii of the substituent elements, but there is no correlation between the <X–O> bond length and the variable Na/Ca site occupancy. The ionic radii of octahedrally coordinated Mg2+ and Mn2+ are such that the shared octahedral–dodecahedral edges are similar in length to the unshared octahedral edges, which is a measure of lattice distortion in garnet structures.

Although the mineral gyrolite has long been known to occur in the British Isles, namely in the basalt lavas of Skye, Mull, and the Treshnish Islands, &c., off the west coast of Scotland, and has more recently been described from the cliffs between Ardtornish Bay and the fault of Dearg Allt in Argyllshire on the mainland, no instance of its occurrence in the lavas of the north of Ireland has hitherto been recorded.

The examination, however, of a large number of specimens collected both for me and by myself during the past year and a half has shown that the mineral, though occurring in small quantity relative to the other zeolites with which it is associated, is fairly widely distributed throughout the harder lavas in the neighbourhood of Belfast.

X-ray and thermal studies in the system MnO-O-H2O show that the transformations groutite(α-MnOOH)-ramsdellite(MnO2)-pyrolusite(MnO2) are topotactic, with the a, b, and c directions of all three corresponding. The reactions proceed by migration of manganese atoms and, where appropriate, protons. Pure single crystals of ramsdellite could not be prepared by heating groutite, even though the two structures are very similar.

In the course of a study of certain cerium minerals, a spectrogram of churchite was taken and it was noticed that the cerium lines were barely visible, whereas the yttrium lines were very strong. We therefore decided to re-investigate this species.

Churchite was originally described by A. H. Church in 1865, and named by C. G. Williams in the same year. The specimens were collected by R. Talling from an unnamed locality in Cornwall. It has only been analysed once, by Church, who showed it to be a hydrated phosphate of rare-earths and lime; his quantitative data have been recalculated and included in table I. Church obtained qualitative reactions for the cerium group of rare-earths, and for cerium itself, but made no attempt to determine the ratio of cerium to yttrium earths; he assumed a mean molecular weight for the rare-earths which would correspond to R2O3 324, essentially a mixture of cerium earths with but little yttria, but did not adduce any evidence for this assumption.

Tricalcium disilicate, first described by Shepherd, Rankin, and Wright in their investigations on the lime–silica and lime–alumina–silica systems has since been reported as a constituent of technical slags. An account has also been given of its occurrence as a reaction product in a glass furnace.

In the ternary system CaO–Al2O3–SiO2 the compound forms with pseudowollastonite–gehlenite and larnite–gehlenite two three-phase equilibrium assemblages, associations which are in part recorded in the technical products.

G. V. Wilson recorded the disilicate together with wollastonite and melilite in reconstituted limestone fragments enclosed in glass, while S. G. Gordon has described and presented an analysis of a slag composed of pseudowollastonite and the 3:2-compound approaching in composition that of the binary eutectic in the synthetic system.

Eight samples (seven volcanic rocks and one quartz sandstone) have been dredged from the Funk Seamount, 60 km NW of Marion Island in the southwest Indian Ocean (lat. 46° 15′S, long. 37° 20′ E). The volcanic rocks are fine-grained vesicular basanitoids and glass-rich volcanic breccias geochemically similar to the Marion Island lavas. Lavas and breccias contain a suite of megacryst minerals and of small polymineralic xenoliths, in both of which kaersutite is a prominent constituent.

The megacryst suite comprises large unzoned single grains of kaersutite, plagioclase, pyroxene, magnetite and ilmenite, all showing textural evidence of resorption/reaction with the basanitoid host. The megacrysts have a limited range of compositions except for the plagioclase which ranges from oligoclase to labradorite.

The small (2 mm to ∼ 3 cm) xenoliths are mostly two-pyroxene amphibole assemblages with or without olivine, magnetite, ilmenite, plagioclase and apatite. The xenoliths show some evidence of reaction with the basanitoid host and most have undergone recrystallization and/or localised decompression melting.

Xenolith and megacryst assemblages are interpreted as being associated with the formation and partial crystallization of a hydrous basanitoid melt at depth.

Fluid flow through a fractured granite core and leaching experiments on granite powder (at constant temperatures of 50 and 100°C and during cooling from 100 to 50°C) indicate that the dissolved silica content of the fluids originates from the dissolution of feldspars and phyllosilicates. The dissolution of quartz is not ruled out but it should be a minor phenomenon. The precipitation of quartz may control the dissolved Si content during constant temperature leaching. During cooling from 100 to 50°C chalcedony, alumino-silicates, and chlorite are all capable of precipitation, possibly leading to some clogging or sealing of fissures.

Ca- and Na-rich pyroxene compositions of four agpaitic phonolites from the Cantal Volcano (France) have been studied. The pyroxenes from each sample show a range of compositions between X2+ pyroxencs (with X = Ca, Mg, Fe2+) and aegirine. The main substitution, X2+ by (Fe3+ + Na+), occurs when Na-Mg = 0.5, by which time Si is already equal to 2.0. The crystallization of Fe-Na-rich pyroxenes seems to be related to the increasing peralkalinity of the environment, in which the initially high temperature was suddenly reduced. Other factors, such as the structure of the liquid, are also considered.

The vicinity of the 490 Ma Cashel gabbroic intrusion experienced pressures of about 4.05 ± 0.2 kbar and temperatures in excess of 850 °C. These conditions caused intense hornfelsing and partial melting of the surrounding Dalradian metasediments. From the study of the progressively changed composition of the aureole hornfelses it is deduced that elements were fractionated into the melts as follows: Si>K>Na>Ca>Mn>Al>Fe>Mg and Rb>Ba>Sr>Ga>Cr,Ni,Co. This order of fractionation, which is the opposite to that in magmatic crystallization, provides a detailed picture of the mode of interaction between a mantle derived basic magma and mid-crustal rocks, illustrating how one type of S-type granite can be produced. The rare earth elements (REE) were both removed and fractionated but Eu largely remained in the crystal fractions giving increasing positive Eu anomalies with rising partial melting and these trends can be explained by the extraction of a granitic melt from the hornfelses. Fission track mapping of U is used to study the behaviour of U within the aureole and the metamorphic recrystallization of detrital brown zircon to pink new zircon. The S-type Cashel microgranite sill is shown to have been derived by anatexis from the Dalradian rocks, to have preserved the Sr isotope ratios of the metasediments at 490 Ma, and not to be of the same composition as the leucosomes in the metasediments.

Embreyite is a new mineral that has been found only in old specimens collected at Berezov, Siberia. The composition is Pb4·97(CrO4)2·00(PO4)1·91.0·75H2O, or Pb5(CrO4)2(PO4)2. H2O based on both wet and electron-probe analyses. Z = I, Dmeas 6·45, Deale 6·41. Crystals are monoclinic with a 9·755 Å, b 5·636, c 7·135, β 103°5′ the space group may be P21/m. No single crystals were found. α = 2·20, β = γ = 2·36. Colour in various shades of orange with a yellow streak. H = 3½; no cleavages observed. Occurs with vauquelinite, crocoite, and phoenicochroite in the oxide zone assemblage from Berezov.

Physical, crystal-chemical and absorption spectroscopical properties of blue tourmalines from a new occurrence in the State of Paraiba, Brazil, are described. Refractive indices, birefringence and specific gravity have been determined as ne = 1.615–1.620, no = 1.632–1.640, Δn=−0.017 to −0.020 and 3.04–3.07g/cm3. Microprobe analyses proved the samples to be elbaites, which are relatively Mn-rich and contain 2.1 wt. % CuO and 0.5 wt. % Bi2O3. Lattice constants are ao = 15.854(4) and co = 7.102(1) Å. The blue colour is due to pleochroic absorption bands of Cu2+ and Mn3+ with maxima at 700 and 520 nm respectively.

Calcium carbonate forms three polymorphic minerals that are found in a variety of environments at the Earth’s surface. Other compounds in the aqueous system can inhibit or enhance the probability of one phase or another, favour growth of specific crystal faces, and change the rate of recrystallization. Control of crystal systems requires understanding of the relationships between the foreign agent and the CaCO3 mineral surface. This work, which examines the transformation of vaterite to calcite, is part of a larger project that aims to define some of the parameters that control calcite recrystallization and grain coarsening.

Microlite-group minerals occur as common replacement products after primary and secondary columbite-group minerals (CGM) in albitised blocky K-feldspar and in coarse-grained, muscovite-rich units of the Schinderhübel I, Scheibengraben and Bienergraben beryl–columbite pegmatites in the Maršíkov District (Silesian Unit, Bohemian Massif, Czech Republic). Textural and compositional variations of microlite-group minerals were examined using electron probe micro-analyses and microRaman spectroscopy (μRS). A complex post-magmatic evolution of the pegmatites and the following microlite populations (Mic) and related processes were found: (1) precipitation of U, Na-rich and F-poor Mic I on cracks in CGM; (2) alteration of Mic I to U-rich together with Na- and F-poor Mic II; and (3) partial replacement of Mic I and II by Mic III with a distinct Na, U and Ti loss and Ca and F gain. Stage (2) includes an extensive leaching of Na, without U loss. The final stage (3) produced euhedral-to-subhedral oscillatory zoned Ca and F enriched Mic III with distinctly different composition to the previous F-poor and A-site vacant Mic II. Aggregates of fersmite are associated commonly with Mic III. Distal Mic IIId occurs locally on cracks in K-feldspar or quartz, with compositions analogous to Mic III. Compositional variations and textural features of microlite-group minerals during dissolution–reprecipitation processes serve as sensitive tracers of post-magmatic evolution in granitic pegmatites recording complex interactions between magmatic pegmatite units and externally derived, hydrothermal metamorphic fluids.

When one optic axis of a biaxial crystal has been located accurately by the usual orthoseopic or conoscopic methods, the second may be located by determining the extinction positions at normal incidence and applying the Biot-Fresnel construction. When use is made of the extinction directions associated with two or more wave normals inclined to the section, this method gives more reliable values of the optic axial angle than can be obtained by the doubling of the angle V over the pole of a bisectrix. If the optic axes have been located with sufficient accuracy by this procedure, then this also determines the orientation of the indicatrix.

New chemical, optical, and X-ray data have been obtained for dumortierite. The unit cell. space group Pemn, contains 4[(Al,Fe)7BSi3O18]. Brown gem quality material from Ceylon has α 1·6860, black, [001], β 1·722, deep redbrown, and γ, 1·7229, brown, with 2Vα 13° , γ > υ. X-ray powder data are given.

Determinations of Cu in separate phases of three olivine-hypersthene and one olivine-bronzite chondrites show that it is very strongly concentrated in the taenite; appreciable amounts are present in the olivine, less in the pyroxene plus plagioclase; it is probable that the copper found in the ‘unattracted, attacked’ fraction is present as metallic copper, and that very little is present in the sulphides.

Kaalijärv is a crater-lake on the estate Kaali (järv = lake in the Estonian language) at 58°24′N., 22°40′E. Known in German as Sall, this locality is 20km. NE. of Arensburg (= Kuresaare) on the Baltic island of Oesel (= Saaremaa). On the level agricultural country a thickly wooded knoll 6–7 metres high is seen. Inside there is a crater 15½ m. in depth, the circular rim of which measures 92–110 m. across. The lake at the bottom is about 60 m. across. The rock of the district is horizontally bedded Silurian dolomite with a covering of glacial deposits. The rim of the crater consists of fragmentary materials, and the steeper inner slopes show the beds of dolomite dipping outwards as a dome at angles of 30–40°. Near by, on an area of ¾ sq. km., are five other smaller craters similar in character, and at least three other depressions that have been filled with stones collected from the tilled fields.