Kamphaugite-(Y) occurs as white to cream-coloured spherical to semi-spherical aggregates of radial crystals in the La Cabrera granitic pluton (Spanish Central System). It mainly occurs on the free surfaces of alkali feldspar, quartz, calcite, kainosite-(Y) and laumontite, and inside miarolitic cavities. La Cabrera kamphaugite-(Y) has an average composition of Ca0.94Y0.89REE0.21(CO3)2 [F0.05(OH)0.95]·1.19H2O. Negative δ13CV-PDB values (–14 to –15‰) indicate a meteoric carbon source. Textural relations between kamphaugite-(Y) and coexisting minerals, its relatively high δ18OV-SMOW values (+25 to +26‰), and the occurrence of laumontite inclusions in kamphaugite-(Y), point to a genesis at < 50°C during very low-temperature post-magmatic hydrothermal activity.

This mineral was originally described as a hydrated copper-arsenate. Analyses of copper-arsenate are given as far back as 1801 by Vauquelin (Journ. des Mines, 1801, X. 562), and by Chenevix in the Philosophical Transactions (for 1801); but at this early date the analyses seem to refer partly to ehalcophyllite and partly to olivenite.

A re-examination of twelve specimens of the Gibeon meteorite has established that the meteorite is basically an octahedrite but has, in several irons of the meteorite, lamellae of kamacite of early origin parallel to the cube. Lamellae containing daubréelite, predating twinning and kamacite exsolution, are common parallel to the cube and rare parallel to the octahedron. A survey of other features failed to suggest any definitely correlated with the anomalous kamacite lamellae.

Compositions concerning sodic amphiboles (glaucophane) in the system Na2O-Al2O3-MgO-SiO2-H2O have been studied at PH2O ≤ 3 kb, 380 °C < T < 700 °C. The study attempts to establish the mineral parageneses under these physical conditions as they define the clay mineral (saponite-hectorite smectite) and greenschist (chlorite-albite) facies. The occurence of sodic amphiboles is defined by compositional parameters. Glaucophane does not appear in the present investigation.

The method of ‘reaction reversal’, i.e. using precrystallized mineral assemblages to form new ones, has been used to establish the three reactions: albite + chlorite → paragonite + saponite, paragonite + chlorite → saponite + cordierite, and saponite + paragonite → albite + cordierite. In general, the clay mineral → greenschist transformation is favoured by an increase in pressure in the system studied. The amphibole present is a sodic richterite with the type substitution

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.

The crystal structure of kyzylkumite, ideally Ti2V3+O5 (OH), from the Sludyanka complex in South Baikal, Russia was solved and refined (including the hydrogen atom position) to an agreement index, R1, of 2.34% using X-ray diffraction data collected on a twinned crystal. Kyzylkumite crystallizes in space group P21/c, with a = 8.4787(1), b = 4.5624(1), c = 10.0330(1) Å , β = 93.174(1)º, V = 387.51(1) Å3 and Z = 4. Tivanite, TiV3+O3OH, and kyzylkumite have modular structures based on hexagonal close packing of oxygen, which are made up of rutile [TiO2] and montroseite [V3+O(OH)] slices. In tivanite the rutile:montroseite ratio is 1:1, in kyzylkumite the ratio is 2:1. The montroseite module may be replaced by the isotypic paramontroseite V4+O2 module, which produces a phase with the formula Ti2V4+O6. In the metamorphic rocks of the Sludyanka complex, vanadium can be present as V4+ and V3+ within the same mineral (e.g.in batisivite, schreyerite and berdesinskiite). Kyzylkumite has a flexible composition with respect to the M4+/M3+ ratio. The relationship between kyzylkumite and a closely related Be-bearing kyzylkumite-like mineral with an orthorhombic norbergite-type structure from Byrud mine, Norway is discussed. Both minerals have similar X-ray powder diffraction patterns.

The Driggith vein is representative of the lead-zinc mineralization in the Caldbeck Fells area, with a primary mineral assemblage consisting of quartz, baryte, calcite, chalcedony, pyrite, arsenopyrite, galena, sphalerire, bournonite, argentian tetrahedrite, and native antimony. Broadly similar assemblages are found in Pb-Zn mineralization of Upper Devonian to Permian age else-where in the Lake District. The paragenetic sequence appears to have been early pyrite and minor arsenopyrite associated with quartz; with later baryte, calcite, sphalerite, and chalcopyrite enclosed by galena. Within the galena occur inclusions of tetrahedrite, bournonite, and native antimony. A later stage of baryte mineralization was followed by the alteration of primary sulphides to secondary minerals. Elsewhere in the Lake District, galena occurring in this association also contains inclusions of native antimony, bournonite, and other sulphosalts, and in this respect differs from galena associated with earlier veins composed dominantly of chalcopyrite, pyrite, and arsenopyrite. The inclusions make a major contribution to the high antimony values reported in trace element analyses of galena from the Lake District. The occurrence of these inclusions, which in some cases display preferred orientation within the host galena, is discussed in terms of phase relations involving PbS and AgSbS2.

The chemistry and optics of the amphiboles in alkaline rocks of Koraput, Orissa, India, are described. The variation in chemical characters of the amphiboles is consistent with the variation in rock composition. With progressive fractionation the mineral shows increasing replacement of magnesium by iron while Ca is not affected by such replacement. The trend in variation is comparable to that in pyroxenes of alkaline basaltic magmas. The entry of Ti into the structure of amphibole appears to be favoured by alumina activity and concentration of Ti in the magma. Optical characters vary with the iron : magnesium ratio and titanium content of the mineral. The water content of the magma had an important influence on the composition of the mafic minerals in the rocks.

Arsenoústalečite is a new mineral discovered in a sample collected from the abandoned Ústaleč deposit near Horažďovice, SW Bohemia, Czech Republic. It occurs as rare anhedral grains, up to 40 μm in size, in a calcite gangue, associated with stibioústalečite, hakite-(Hg), berzelianite and uraninite. Arsenoústalečite is dark grey, with a metallic lustre. Mohs hardness is ca. 3½–4; calculated density is 5.730 g/cm3. In reflected light, arsenoústalečite is pale grey with a yellowish shade; it is isotropic. Internal reflections were not observed. Reflectance values for the four COM wavelengths in air [R (%) λ (nm)] are: 33.3 (470); 33.1 (546); 33.0 (589); and 32.9 (650). The empirical formula of arsenoústalečite is (Cu5.81Ag0.17)Σ5.98(Cu5.95Fe0.02Zn0.02Hg0.01)Σ6.00(As1.40Sb0.87Te1.73)Σ4.00(Se10.30S2.32)Σ12.61. The ideal formula is Cu12(As2Te2)Se13, which requires (in wt.%) Cu 34.76, As 6.83, Te 11.63, Se 46.78, total 100.00. Arsenoústalečite is cubic, I$\bar{4}$3m, with unit-cell parameters a = 10.6580(19) Å, V = 1210.7(6) Å3 and Z = 2. The strongest reflections of the calculated powder X-ray diffraction pattern [d, Å (I, %) hkl] are: 3.077 (100) 222, 2.848 (10) 321, 1.946 (12) 521, 1.884(52) 440 and 1.608(21) 622. According to the single-crystal X-ray diffraction data (R1 = 0.0285 on the basis of 334 unique reflections with Fo > 4σFo and 24 refined parameters), arsenoústalečite is isotypic with other tetrahedrite-group minerals. The crystal structure of co-existing stibioústalečite, with an empirical formula of (Cu5.69Ag0.07)Σ5.76(Cu5.80Zn0.13Fe0.06Hg0.01)Σ6.00(Sb1.82As0.42Te1.76)Σ4.00(Se9.52S3.10)Σ12.62 and unit-cell parameters a = 10.6975(16) Å, V = 1224.2(5) Å3 and Z = 2, was refined to R1 = 0.0191 on the basis of 267 unique reflections with Fo > 4σFo and 24 refined parameters. Structural relationships and crystal-chemistry of both members of the ústalečite series are discussed. Arsenoústalečite is named after its type locality, the Ústaleč deposit and its chemical composition. The mineral and its name have been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA2022-116).

The recently defined arctite supergroup contains nine mineral members defined as hexagonal intercalated antiperovskites, most of which have been found in pyrometamorphic rocks of the Hatrurim Complex, Israel. Three members of this supergroup: nabimusaite, gazeevite and zadovite, were identified for the first time in altered carbonate–silicate xenoliths from the Caspar and Scherer quarries, Bellerberg volcano in Germany. Present work focuses on the chemical, structural and spectroscopic investigation of these minerals and their correlation with holotype counterparts. The apparent differences are mainly related to the chemical composition, types of substitution in the tetrahedral and antiperovskite layers within the crystal structure, and position of bands in the Raman spectra. In the Bellerberg volcano xenoliths, the crystallisation of nabimusaite and gazeevite is caused by high-temperature alteration of early mineral associations (clinker-like phases) and their reaction with melt or gas generated by volcanic activity. In turn, the formation of zadovite is related to the Ba-rich silicate melt that filled the intergranular space between the rock-forming minerals.

In X-ray studies of fireclays we have frequently observed the presence of anatase to the extent of 1 or 2% with little or no rutile, and no brookite. Chemical analyses of these clays usually record 1–2% of TiO2 and occasionally more (Ennos and Scott, 1924). The mineralogical form of the TiO2 is usually not stated, but a number of references to the observance of rutile needles give the impression that rutile is the form in which titania occurs in these deposits. Our own observations based on X-ray powder photographs lead us to conclude that anatase is commonly present and that rutile is either absent or present in smaller quantities. We have not detected brookite.

Some small isolated crystals from the gem-washings in Ceylon, recently sent by Mr. A. K. Coomáraswámy to the British Museum for determination and study, were at first thought to be rutile, but on detailed examination proved to be zircon of a rather unusual type. This has a specific gravity of 4.0, which is not increased when the crystals are heated.

The majority of the crystals are from the Balangoda district in the Sabaragamuwa province, and, according to Mr. Coomáraswámy have been derived from a group of zircon-granites which occur in this district; a few others are from Walaweduwa in the Bamberabotnwa district, and from the Hatton district. Associated with them are zircons of more usual types (see p. 48); the present description is, however, confined to the crystals of lower specific gravity.

The plagioclase which forms the subject of this investigation was presented by Dr. C. Stansfield Hitchen, director of the Kenya Geological Survey, who has kindly sent the following note of its occurrence:

Specimens of quartz-muscovite-schist obtained fro: boulders in the Shotover river, western Otago, New Zealand, ere recently examined by the writer and found to contain abundant piedmontite, a mineral not previously recorded from New Zealand. The specimens had been collected twenty years before and were labelled ' micaceous quartz schist coloured with haematite' in the geological collections of the Otago University. The following description is submitted pending further field investigations.

Bystrite is redefined as a four-layer cancrinite-group mineral with the four-layer Losod-type framework and the end-member formula Na7Ca(Al6Si6O24)S52–Cl–. The mineral is known only at the Malo–Bystrinskoe gem lazurite deposit, Baikal Lake area, Siberia, Russia. The associated minerals are calcite, lazurite, sodalite, fluorapatite, phlogopite, diopside, dolomite and plagioclase. Bystrite is brittle, with the Mohs hardness of 5 and distinct cleavage on {10$\bar{1}$0}. The yellow colour of bystrite is due to the presence of S52– anions occurring in Losod (LOS) cages of the aluminosilicate framework with the ABAC stacking sequence. Measured and calculated density is, respectively, 2.43(1) and 2.412 g cm–3 for the holotype and 2.42(1) and 2.428 g cm–3 for the cotype sample. Bystrite is uniaxial (+), ɛ = 1.660(2) and ω = 1.584(2). The mineral was characterised by infrared and Raman spectra. The empirical formulae of the holotype and cotype samples are Na6.97K0.04Ca0.98(Si6.03Al5.97O24)(S52–)0.93[(SO42–)0.15Cl0.83] and Na6.75K0.04Ca1.11(Si6.09Al5.91O24)(S52–)1.04[(HS–)0.17Cl0.85], respectively. Bystrite is trigonal, space group P31c. The unit-cell parameters are: a = 12.8527(6) Å, c = 10.6907(5) Å, V = 1529.4(1) Å3 and Z = 2. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 4.821 (32) (102), 3.915 (38) (211), 3.712 (100) (300), 3.307 (50) (212), 2.782 (18) (400), 2.692 (22) (401), 2.673 (30) (004) and 2.468 (23) (402). Isomorphism and genesis of bystrite-type minerals is discussed. Bystrite and its K,HS-analogue sulfhydrylbystrite, Na5K2Ca(Al6Si6O24)S52–(HS)–, are indicators of highly reducing conditions.