Anisotropic opaque minerals viewed in reflected light microscopy show two sets of colours: the colours seen in plane polarized light which change as the section is rotated on the microscope stage, and the colours seen between crossed polars which change as the analyser is uncrossed. These latter colours are known variously as polarization colours or anisotropic rotation tints, but are here referred to as anisotropy colours. They are commonly a diagnostic aid to correct mineral identification. All these colours occur as a consequence of the dispersion of the relative permittivity (dielectric) tensor—the variation in the values of the tensor with wavelength of incident light and in low symmetry crystals, the variation in the directions of the principal axes of the tensor with wavelength.

In this paper, it is shown that the colour seen in plane polarized light and the anisotropy colours can be predicted for any orientation of section, at any stage angle, and for any degree of uncrossing of the analyser by calculations based on the dielectric tensor values, and these predicted colours compare favourably with the observed values. Three minerals are studied in this paper as examples: stannite, covelline, and bournonite.

This paper gives an overview of the geosphere research studies being undertaken by the Radioactive Waste Management Directorate (RWMD) of the Nuclear Decommissioning Authority. The approach of the RWMD in the current generic phase of the UK managing radioactive waste safely (MRWS) programme is to maintain an understanding of key processes and to carry out research and development into techniques so capability can be built. Although RWMD can demonstrate a general understanding of geosphere processes at this stage in the UK project, it is recognized that this will need to be made site-specific as the MRWS programme progresses. An understanding of the geosphere at the selected site(s) will be an important part of the future programme. Where possible, the RWMD will participate in international studies so that relevant site-based information can be accessed. In this way, the RWMD will be prepared for site-specific work in stage 5 of the MRWS process.

The rare mineral nadorite has hitherto been recorded from one locality only, namely, Jebel Nador in the province of Constantine, Algeria, where at one time it was found in considerable quantity associated with bindheimite, smithsonite, and galena in a deposit lying between lacustrine limestone and brown marl.

In the present notes I am able to record the occurrence of this mineral at the small antimony mine of Bodannon, St. Endellion, Cornwall, where I found a single specimen in 1907. Immediately after the reading of this paper, Professor A. Hutchinson of Cambridge most kindly sent me a specimen for examination which he had himself collected from the small dump at Bodannon in 1919, and this mineral, which had attracted his attention, also proved to be nadorite.

Labradorite of exceptional purity, occurring as phenocrysts in two basaltic dikes just below the lighthouse at St. John's Point, Ardglass, County Down, Northern Ireland, was described by Professor A. Hutchinson and myself in 1912. The refractive indices for sodium-light were determined on an Abbé-Pulfrich total-reflectometer. Carefully selected material was analysed by Mr. G. G. Knighton and by Mr. M. C. Burkitt, and the specific gravity of the material analysed was determined.

Rocks composed mainly of the hydrated ferrous silicate greenalite are of very restricted geological and geographical distribution and, up to the present, have been recognized only from certain of the pre-Cambrian sedimentary iron-bearing formations of the Lake Superior region. It is of interest, therefore, to record an additional occurrence, not only from another region but from a later geological system.

The implementation of a geological disposal facility requires the demonstration of confidence that such a facility would be safe during both the operational period and in the long-term after the closure of such a facility. The generic environmental safety case described in this paper is the vehicle used to demonstrate an understanding of environmental safety. It will be used to prepare a site-specific environmental safety case in due course. The approach taken will be consistent with a staged development and approval process, as advocated by the environmental regulators.

Probably first found in Arabia, then Moctezuma, Sonora (the type locality), finally at Tombstone, Arizona. Crystals are cubic, invariably octahedral in habit, up to 2 mm in size. Colour forest green (RHS 136A), H = 3, D = 6.4.

Wet chemical analysis gave CuO 11.0%, PbO 33.0, TeO2 50.7, H2O 3.4; soluble in cold dilute acids. The strongest lines are 7.223(5), 4.170(2), 3.614(3), 3.472(4), 3.343(6), 3.036(10), 7.952(3), 2.454(5) Å. The cell indexes as cubic, a = 12.519 Å; for Z = 12, ρcalc = 6.41 g/cm3. May be anisotropic in thin section with birefringence up to 0.011; n = 2.04.

James Sowerby in his ‘British Mineralogy’ describes and figures sider the head of ‘Argilla electrica’ or ‘White Tourmaline’ a mineral which was undoubtedly phenacite. The specimen was sent to Sowerb,y by a Mr. Herbert in 1804, and was said to have been found in a mine in St. Just, Cornwall. According to Sowerby's description and from the eoloured plate which he gives of the specimen, the mineral occurred as long-prismatlc, colourless crystals , some of which were doubly terminated and lying upon and partly penetrated by mass of prismatic quartz crystals. The crystals were ‘so divided by cracks and flaws in general as to appear of an opaque whiteness in parts’.

A new mineral species, holubite, ideally Ag3Pb6(Sb8Bi3)Σ11S24, has been found at Kutná Hora ore district, Czech Republic. The mineral is associated with other lillianite homologues (gustavite, terrywallaceite, vikingite and treasurite) most frequently as grain aggregates and replacement rims of earlier Ag–Pb–Bi minerals, growing together in aggregates up to 200 × 50 μm. It typically occurs in a close association with Ag,Bi-bearing galena and terrywallaceite. Holubite is opaque, steel-grey in colour and has a metallic lustre, the calculated density is 5.899 g/cm3. In reflected light holubite is greyish white and bireflectance and pleochroism are weak with grey tints. Anisotropy is weak to medium with grey to bluish-grey rotation tints. Internal reflections were not observed. Electron microprobe analyses yielded an empirical formula, based on 44 atoms per formula unit (apfu) of (Ag3.03Cu0.03)Σ3.06(Pb6.19Fe0.02Cd0.01)Σ6.22(Sb7.71Bi2.90)Σ10.61S24.12. Its unit-cell parameters are: a = 19.374(4), b = 13.201(3), c = 8.651(2) Å, β = 90.112(18)°, V = 2212.5(9) Å3, space group P21/n and Z = 2. Holubite is a new member of the andorite branch of the lillianite homologous series with N = 4. The structure of holubite contains two Pb sites with a trigonal prismatic coordination, eight distinct octahedral sites, of which one is a mixed (Bi,Ag) site and one is a mixed (Sb,Pb) site, and twelve anion sites. Holubite is defined as a lillianite homologue with the three following requirements: N = 4, L% [Ag+ + (Bi3+,Sb3+) ↔ 2 Pb2+ substitution] ≈ 70% and approximately one quarter to one third at.% of antimony is replaced by bismuth [Bi/(Bi+Sb) ≈ 0.26–34]. The new mineral has been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA2022-112) and named after Milan Holub, a key Czech geologist and specialist in the Kutná Hora ore district.

The diffusive exchange of dissolved material between fluid flowing in a fracture and the enclosing wallrocks (rock matrix diffusion) has been proposed as a mechanism by which radionuclides derived from a radioactive waste repository may be removed from groundwater and incorporated into the geosphere. To test the effectiveness of diffusive exchange in igneous and metamorphic rocks, we have carried out an investigation of veins formed at low temperatures (<100°C), comparing the oxygen isotopic composition of vein calcite with that of secondary calcite in the wallrocks. Two examples of veins from the Borrowdale Volcanic Group, Cumbria, and one from the Mountsorrel Granodiorite, Leicestershire, UK, have remarkably similar vein calcite compositions, ca. +20‰(SMOW) or greater, substantially heavier than the probable compositions of the host rocks, and these vein calcite compositions are inferred to reflect the infiltrating fluid and the temperature of vein formation. Calcites from the wallrocks are similar to those in veins, with little evidence for exchange with the wallrocks. The results support existing models for this type of vein which suggest low-temperature growth from formation brines originally linked to Permian or Triassic evaporites. The results are consistent with flow through fractures being attenuated through a damage zone adjacent to the fracture and provide no evidence of diffusional exchange with pore waters from wallrocks.

The Devonian Hera metaturbidite-hosted polymetallic Au–Zn–Pb–Ag deposit of central NSW, Australia, contained a total undepleted resource of 3.6 Mt @ 3.3 g/t Au, 25 g/t Ag, 2.6% Pb and 3.8% Zn. The deposit comprises a number of distinctive lodes with each containing a distinctive ore and alteration/gangue mineralogy, though generally the sulfide ore comprises various mixtures of sphalerite, galena, chalcopyrite, pyrrhotite and relatively common visible gold–electrum. The North Pod and Far West lodes are distinctly Sb rich and contain a more diverse ore mineralogy with arsenopyrite, native silver, native antimony, gudmundite, tetrahedrite-(Fe), argentotetrahedrite-(Fe), acanthite, dyscrasite, nisbite and breithauptite. From analysis of 52,760 assays from across the deposit it was found that there was a very poor correlation between gold and each of Fe, Zn, S, Pb, Cu, As and Ag, whereas Ag correlated reasonably well with both Pb and Zn. Results from EPMA shows that gold varies widely in composition from host-rock associated gold (96 wt.% Au) through more intermediate compositions (88–73 wt.% Au) to electrum (46–27 wt.% Au), commonly associated with Sb-phases and containing significant Sb within the gold itself (1.05–2.58 wt.% Sb). From the Far West lense, aurostibite occurs as distinctive rims around gold. Although aurostibite associated with gold contains no silver, the gold itself contains constant moderate amounts (10.87–12.27 wt.% Ag). We suggest that the aurostibite and other Sb phases formed from a late-stage Sb-rich hydrothermal during low-temperature retrograde skarn alteration. There is abundant evidence for both chemical and physical remobilisation at Hera and this remobilisation is largely responsible for the spectrum of gold compositions observed. The source for these fluids may be an underlying magmatic body, evidence for which occurs as granite pegmatite dykes in various locations throughout the deposit. Furthermore, gold with a moderate to high Sb content may be indicative of a low temperature of formation.

Piccoliite, ideally NaCaMn3+2(AsO4)2O(OH), is a new mineral discovered in the Fe–Mn ore hosted in metaquartzites of the Montaldo di Mondovì mine, Corsaglia Valley, Cuneo Province, Piedmont, Italy. It occurs as small and rare black crystals and aggregates hosted by a matrix of quartz, associated with calcite and berzeliite/manganberzeliite. It has been also found in the Valletta mine near Canosio, Maira Valley, Cuneo Province, Piedmont, Italy, where it occurs embedded in quartz associated with grandaite, hematite, tilasite/adelite and rarely thorianite. The mineral is opaque (thin splinters may be very dark red), with brown streak and has a resinous to vitreous lustre. It is brittle with irregular fracture. No cleavage has been observed. The measured Mohs hardness is ~5–5.5. Piccoliite is non fluorescent. The calculated density is 4.08 g⋅cm–3. Chemical spot analyses by electron microprobe analysis using wavelength dispersive spectroscopy resulted in the empirical formula (based on 10 anions per formula unit) (Na0.64Ca0.35)Σ0.99(Ca0.75Na0.24)Σ0.99(Mn3+1.08Fe3+0.59Mg0.20Ca0.10)Σ1.97(As2.03V0.03Si0.01)Σ2.07O9(OH) and (Na0.53Ca0.47)Σ1.00(Ca0.76Na0.23Sr0.01)Σ1.00(Mn3+0.63Fe3+0.49Mg0.48Mn4+0.34Ca0.06)Σ2.00(As1.97P0.01Si0.01)Σ1.99O9(OH) for the Montaldo di Mondovì and Valletta samples, respectively. The mineral is orthorhombic, Pbcm, with single-crystal unit-cell parameters a = 8.8761(9), b = 7.5190(8), c = 11.689(1) Å and V = 780.1(1) Å3 (Montaldo di Mondovì sample) and a = 8.8889(2), b = 7.5269(1), c = 11.6795(2) Å, V = 781.43(2) Å3 (Valletta sample) with Z = 4. The seven strongest powder X-ray diffraction lines for the sample from Montaldo di Mondovì are [d Å (Irel; hkl)]: 4.85 (57; 102), 3.470 (59; 120, 113), 3.167 (100; 022), 2.742 (30; 310, 213), 2.683 (53; 311, 023), 2.580 (50; 222, 114) and 2.325 (19; 320, 214, 223). The crystal structure (R1 = 0.0250 for 1554 unique reflections for the Montaldo di Mondovì sample and 0.0260 for 3242 unique reflections for the Valletta sample) has MnO5(OH) octahedra forming edge-shared dimers; these dimers are connected through corner-sharing, forming two-up-two-down [[6]M2([4]TO4)4φ2] chains [M = Mn; T = As; φ = O(OH)] running along [001]. These chains are bonded in the a and b directions by sharing corners with AsO4 tetrahedra, giving rise to a framework of tetrahedra and octahedra hosting seven-coordinated Ca2+ and Na+ cations. The crystal structure of piccoliite is closely related to that of pilawite-(Y) as well as to carminite-group minerals that also show the same type of chains but with different linkage. The mineral is named after the mineral collectors Gian Paolo Piccoli and Gian Carlo Piccoli (father and son) (1926–1996 and b. 1953, respectively), the latter having discovered the type material at the Montaldo di Mondovì mine.