Copper mineralization at Tomnadashan is associated with granitic lenses intruded into a small Caledonian diorite body. The mineralization occurs as disseminations and irregular veinlets and mainly comprises pyrite, chalcopyrite, tetrahedrite-tennantite, calcite, and quartz. There are small inclusions of bismuthinite, galena, aikinite [(Cu,Pb,Fe,Bi)S3], and a mineral with a chemistry similar to hodrushite (Cu8Bi12S22). The tetrahedrite contains up to 6.1 wt. % bismuth.

Four km to the south, at Corrie Buie, are quartz veins, hosted by meta-limestones, containing galena with minor amounts of chalcopyrite, pyrrhotite, sphalerite, electrum, schirmerite, and lillianite homologues.

The mineralogy of both deposits is consistent with that associated with acid magmatism. There are mineralogical similarities between the two deposits but the style of mineralization at Tomnadashan suggests a limited hydrothermal system and therefore the Corrie Buie veins may be related to felsic intrusives to the south.

Grandidierite occurs in the outer margin of a biotite-rich pelitic xenolith in norite close to the contact of a tourmaline-bearing granite in the Haddo House norite-gabbro complex. The boron for the grandidierite was derived by metasomatism from the granite. The assemblage is (decreasing order): An55–51 plagioclase (65%), biotite (10%), spinel (10%), cordierite (5%), corundum (5%), ilmenite, grandidierite (< 1%), rutile, sphene, zircon. XMg range is grandidierite (0.80–0.78) > cordierite (0.78) > biotite (c. 0.59) > spinel (0.35–0.27). The grandidierite has little chemical variation: SiO2, 19.9–20.5%; Al2O3, 51.3–51.9%. A compilation of all grandidierite analyses in the literature shows that the only substitutions are Fe2+ ⇌ Mg and Al ⇌ Fe3+, the XMg range being 0.98 to 0.19.

Jeppeite, a new mineral, similar in composition to and overgrown on priderite, has been found in the lamproite plug of Walgidee Hills (18° 19′ S, 124° 51′ E), Western Australia. The mineral is named for the discoverer, Dr J. Jeppe. It is monoclinic, C2/m, a 15.453 b 3.8368 c 9.123 Å β 99.25°, strongest powder lines 4.50(002) (4), 3.07(310) (10), 2.99(003,31) (10), 2.961(20) (4), 2.812(311,112) (10), 2.091 (6), 2.074 (6), 1.919 (8) similar to artificial K2Ti6O13. The sparse eluvial crystals are black, elongated along b, bounded by {100}, {20} faces (Λ 45°) and {010}; perfect 100 and good 20 cleavages or partings, submetallic lustre, pale-brown streak, brittle, and cleave into (100) flakes. Dobs 3.94, Dcalc 3.98. Colour values for illuminant C from reflectance spectra for Rp, Rb, and Rθ are: Y% 13.3, 14.4, 16.6; λd 474, 473, 475; and Pe% 5.1, 4.5, 4.3. Refractive indices from reflectances at 590 nm in air are 2.13, 2.21 and 2.35. In thin section, αΛα10° blue, β = b dark greenish brown almost to black, γ = c brown. Bireflectance and birefringence positive. H 5–6, VHN100 orientation dependent; for indentations normal to b 664–773.

Jeppeite is common in the lamproite as prismatic to acicular aggregates associated with priderite, richterite, shcherbakovite, wadeite, perovskite, and apatite in a green and white celadonite and chlorite matrix, with a little calcite and sphene, after olivine, pyroxene, and leucite.

Electron probe analysis, using Fe, Ti, nepheline, and benitoite standards, gave K2O 8.47, BaO 17.35, TiO2 69.29, Fe2O3 (total Fe) 4.74, sum 99.85%; (Mg, Na, Zr detected). This analysis calculates to (K1.15,Ba0.73)Σ1.88 (Ti5.56, Fe3+0.38)Σ5.94O13, or ideally, (K,Ba)2(Ti,Fe)6O13.

Sweetite, naturally occurring Zn(OH)2 with tetragonal symmetry, has been found at Milltown, near Ashover, Derbyshire. It occurs as colourless or whitish bipyramids up to 1 mm in size scattered over the surface of colourless fluorite cubes. The cell dimensions are α 8,222 and c 14.34Å with Z = 20. The strongest lines of the X-ray powder pattern are (d, I, hkl): 4.53 37 (112); 3.572 60 (004,202,211); 2.922 100 (213,220); 2.708 18 (105,204); 2.257 17 (224,215,321); 1.840 11 (226,420,413); 1.764 24 (316). Sweetite is uniaxial negative, ω 1.635, ɛ 1.628. Dmeas is close to 3.33 and Dcalc 3.41. Chemical analysis gave 84.3% ZnO and 17.0% H2O, while theoretical figures for Zn(OH)2 are 81.9 and 18.1% respectively.

Eggletonite is a new mineral, the Na analogue of ganophyllite. Type material has composition

(Na0.82K0.40Ca0.39□0.39)Σ2.00 (Mn6.61Zn0.08Mg0.16Fe0.61Al0.56)Σ8.02 (Si10.33Al1.67)Σ12.00[(O28.92(OH)3.08]Σ32.00 (OH)4.00·10.66H2O.

It occurs as prismatic crystals elongated along [100] in miarolitic cavities in nepheline syenite at the Big Rock Quarry, Little Rock, Arkansas. Single-crystal X-ray diffraction data are consistent with space group I2/a or Ia; a = 5.554, b = 13.72, c = 25.00Å, β = 93.95° Z = 2; this is equivalent to the substructure of ganophyllite. Physical properties include cleavage: {001} perfect; colour: dark brown; translucent; streak: light brown; hardness (Mohs): 3–4; brittle; observed density 2.76, calculated density 2.76 g/cm3. Optically, eggletonite is biaxial negative, with optical parameters 2Vα = 9(3)° r < ν, weak; indices of refraction α = 1.566(2), β = 1.606(2), γ = 1.606(2); pleochroism is very weak, γ ≃ β > α; α = pale brown to colourless, β ≃ γ = pale yellow brown. Principal lines in the X-ray powder diffraction pattern are (d, I/Io): 12.4, 100; 3.45, 15; 3.13, 30; 2.854, 15; 2.691, 25; 2.600, 20; 2.462, 20; 2.387, 15. The name is in honour of Dr Richard A. Eggleton, Australian National University.

The Carnmenellis granite and its aureole contain the only recorded thermal groundwaters (up to 52 °C) in British granites. They occur as springs in tin mines at depths between 200 and 700 m and most are saline (maximum mineralization 19 310 mg 1−1). Mining activity has disturbed the groundwater circulation pattern developed over a geological time-scale and levels of bomb-produced tritium (> 4 TU) indicate that a significant component (up to 65 %) of the most saline waters are of recent origin. All components of all the mine waters are of meteoric origin. Radiogenic 4He contents, 40Ar/36Ar ratios, and uranium series geochemistry suggest that the thermal component has a likely residence time of at least 5 × 104 years and probably of order 106 years.

The thermal waters have molar Na+/Cl− ratios considerably less than 1 but they are enriched relative to sea water in all major cations except Mg. The groundwater is also particularly enriched in Li with contents ranging up to 125 mg 1−1. The groundwater salinity, which may reach a maximum of 30 000 mg 1−1, is shown to result from weathering reactions of biotite (probably through a chloritization step) and plagioclase feldspar, to kaolinite. On volumetric considerations, fluid inclusions cannot contribute significantly to the groundwater salinity, and stable isotope ratios rule out any contribution from sea water.

Groundwater silica contents and molar Na+/K+ ratios suggest that the likely equilibration temperature is 54°C, which would imply a depth of circulation of about 1.2 km.

Blue-coloured gem-quality spinel from Nigeria was analysed by wet chemical methods (using atomic absorption spectrophotometry) and investigated by X-ray diffraction. The results showed it to be gahnite (unit cell dimension a=8.091±0.003 Å) containing 36.7% ZnO, 3.58% FeO, and 0.12% MgO. The spinel has an RI of 1.79 and density between 4.4 and 4.59. Broadening of the n[111] XRD reflections indicates a measure of compositional heterogeneity. The gahnite analyses were compared with compositions of zinc spinels from other parts of the world. The analyses cluster into two distinct groups, Mg-rich spinels of metamorphic origin and Mg-poor spinels (including the Nigerian gahnite) with igneous affinities. Diadochy seems to operate within the zinc spinel structure between (Zn + Mn) and (Fe + Mg).

Nelenite, (Mn,Fe)16si12O30(OH)14[O6 (OH)3], is a polymorph of schallerite and a member of the friedelite group. X-ray diffraction patterns can be indexed on a supercell with a = 13.418(5) and c = 85.48(8)A, space group Rm, but by analogy with TEM results on mcGillite and friedelite, the structure is based on a one-layer monoclinic cell with a = 23.240, b = 13.418, c = 7.382 Å, β = 105.21°, and space group C2/m. Chemical analysis yields SiO2 31.12, FeO 17.12, MgO 0.12, ZnO 3.63, MnO 29.22, As2O3 12.46, H2O 6.42, sum = 100.09%. Analysis of a number of samples indicates that Fe substitutes for Mn up to 5.8 of the 16 octahedrally coordinated cations, but that the Si: As ratio is constant. The strongest lines in the X-ray powder diffraction pattern (d, I/Io) are: 2.552,100; 2.878,70; 1.677,60; 3.55,60; 1.723,50.

Nelenite is brown in colour with a vitreous luster and perfect {0001} cleavage, which easily distinguishes it from schallerite. The Mohs' hardness is approximately 5. The density is 3.45 g/cm3 (calc.) and 3.46 g/cm3 (obs.). Nelenite is uniaxial negative with ɛ = 1.700 and ω = 1.718 (both ± 0.004). Nelenite was formerly known as ferroschallerite, which is a misnomer. It was found in the Franklin Mine, Franklin, Sussex County, New Jersey, in the 1920s. It occurs in several parageneses, associated with actinolite, tirodite, albite, garnet, feldspars, and several members of the stilpnomelane group in coarse-grained assemblages with pegmatitic texture and a breccia likely derived from this rock. Nelenite is named in honour of Joseph A. Nelen, chemist at the Smithsonian Institution.

A Zn- and Y-group-bearing senaite, formulated as AM21O38 (Pb0.63Na0.46Ba0.11)Σ1.20(Ti14.64Zn1.74Y‒group REE0.70Mn0.38Nb0.20Sn0.03Zr0.03Th0.02)Σ20.9O38, a member of the crichtonite group, is a newly characterized phase associated with murataite at the St Peters Dome area, Colorado. The Zn- and Y-group-bearing senaite is uranium-free and nonmetamict, but otherwise is comparable to known senaites and davidites in X-ray diffraction pattern, symmetry, and structure. The REE distribution shows a strong dominance of Y and the Y-group REE which are present in M(1). Megascopically, the mineral is black, submetallic, and opaque; in polished section it appears to be white and moderately bright compared with murataite. Cleavage is absent but twinning on {520} is present.

Senaite and hitherto unreported zinc-bearing senaite from Dattas, Diamantina, Minas Gerais, Brazil, have the following respective structural formulas as determined by electron microprobe:

(Pb0.76Sr0.20La0.08Ce0.07Ba0.04)Σ1.15(Ti12.89Mn0.88Y0.59Zn0.12Mg0.07Nb0.03Cr0.02Th0.02)Σ20.61O38

and

(Pb0.89Ba0.15Ce0.02Sr0.02)Σ1.08(Ti14.57Zn1.76Na0.63Mn0.50Y0.28Nb0.14Mg0.04Cr0.02)Σ20.83O38

The thermal expansions of trimerite and beryllonite have been determined up to 800°C. No anomalies were observed in the thermal expansion curves but the expansion coefficients for beryllonite are approximately twice those of trimerite. The thermal expansion behaviour of the minerals is interpreted in terms of a tetrahedral tilting model with the main change in apparent tilting being about the monoclinic 010 plane, i.e. the 0001 pseudo-hexagonal plane.

The historical background leading to the discovery of sarcolite by Thomson is reviewed. Many mineralogical reference works quote Thompson (1807) but no paper on sarcolite by Thomson has been found; also the spelling of Thomson is incorrect on numerous occasions. The history of sarcolite from its original discovery is reviewed. Chemically, sarcolite is inadequately characterized in spite of a structural study by Giuseppetti et al. (1977). All known chemical analyses are collated and discussed. Two new analyses, using a combination of gravimetric, colorimetric, atomic absorption, and electron probe methods, are presented which show sarcolite to contain 2 wt. % flourine. The presence of this element in sarcolite was reported in 1860 but no quantitative data given; the new determinations cast some doubt over certain aspects of the sarcolite structure.

Measured densities of sarcolite range from 2.93 to 2.96 (mean 2.95) gm/cm3; the tetragonal unit cell of a 12.32 and c 15.48 Å leads to a calculated density of 2.925 gm/cm3 using the empirical formula. Empirically sarcolite may be expressed as:

Na1.38Ca6.0(Ca0.37,K0.13,Fe0.08,Sr0.07,Mg0.05)Σ0.70 Al3.90Si6.02P0.54O26.20F1.06C0.06

and ideally

Na2Ca12(Ca,K,Fe,Sr,Mg)2Al8Si12(P,Si)O52F2

and suggests 27 (oxygen and fluorine) atoms in the quarter unit cell.

Details are given of the mineralogical assemblage, optical properties, infra-red and thermal behaviour of sarcolite which, after 176 years, is still known from only one locality—Monte Somma.

Macphersonite is white, resinous to adamantine, hardness (Mohs) 2½−3, density 6.50–6.55 gm/cm3 and possesses a perfect cleavage on {010}. Optically it is negative with 2Vα 35–36°, α = 1.87, β = 2.00 and γ = 2.01, α = b, γ = c, and γ = a, dispersion r > v. Polysynthetic twinning, with either coarse or fine lamellae, is common, as are contact twins. Crystals are orthorhombic, tabular on b with a 10.37, b 23.10 and c 9.25 Å, cell volume 2215.8 Å3 and space group Pcab; Z is 8 formula units. The seven strongest lines in the X-ray powder pattern are 3.274 (50) 052; 3.234 (100) 251; 2.654 (90) 351,203; 2.598 (30) 172, 400; 2.310 (30) 004, 371, 0.10.0; 2.182 (30) 263; and 2.033 (30) 234, 452, 154, 1.10.2. Electronprobe-microanalysis-determined chemistry leads to the empirical formula (Pb4.08, Cu0.10, Cd0.07)Σ4.25S0.90 C2.18O10.55(OH)1.58 which yields the ideal formula Pb4(SO4)(CO3)2(OH)2 and hence macphersonite is a polymorph of leadhillite and susannite. The infrared spectrum shows basic similarities to leadhillite and susannite spectra with additional diagnostic absorption bands. Macphersonite shows an identical thermogravimetric behaviour to that of leadhillite. It is associated, in varying combinations, with leadhillite, susannite, cerussite, caledonite, pyromorphite, scotlandite, galena, and the ‘lead hydroxyapatite’ of Temple (1955). The new mineral mimics leadhillite.

Dypingite, Mg5(CO3)4(OH)2·5H2O, was found in materials obtained during the production of high purity magnesia from crude magnesite by the calcination/CO2-leaching process. The snow-white, finely crystalline dypingite contained 41.0% MgO; the theoretical value is 41.5%. The X-ray powder data revealed a long period structure with a strong peak at 31.0 Å. The five strongest reflections (Å) and their estimated intensities (I/I0) were 10.4 (100), 31.0 (40), 15.62 (40), 5.86 (30), and 6.34 (20). The DTA curve showed ten endothermic reactions with maxima at 43, 50, 77, 86, 105, 127, 180, 260, 420, and 514°C and an exothermic reaction at 495°C.

An occurrence of a celadonite-like mineral in a weathered basalt in the Lake District has been investigated by X-ray diffraction, X-ray fluorescence, electron microprobe, and infra-red spectroscopic methods. The bulk composition of the mineral corresponds to an aluminous-glauconite. The data show that the mineral is most probably a celadonite-muscovite or celadonite-illite mixture, although a celadonite-phengite cannot be entirely discounted. Approximately 10% smectite layers are also present. The results suggest that re-examination of many aluminous glauconites may show them to be mixtures of this type.

Electron microprobe analysis of the new mineral scotlandite yielded Pb 72.27, S 9.95, corresponding to PbO 77.85, SO2 19.88, sum 97.73 wt.%. Secondary ion mass spectrometry showed the absence of Li, Be, B, C, N, and F, but the presence of very small amounts of Br. Infrared spectroscopy showed that the mineral is a sulphite with neither OH nor any other polyatomic anions. The empirical formula, calculated on the basis of Pb+S = 2 is Pb1.06S0.94O2.94 or ideally PbSO3.

The mineral has the following vibrations of the sulphite ion in the infrared spectrum: v3 920, 865; v1 970 (?); v2 620, 600; v4 488, 470 cm−1.

Scotlandite is monoclinic, with possible space groups P21 or P21/m. The unit cell dimensions are: a 4.542(2), b 5.333(2), c 6.413(2) Å, β 106.22(4)°, Z = 2. The strongest lines in the powder diffraction pattern are: 3.99(10) (011), 3.38(7) (110), 3.25(8) (11), 3.07(4) (002), 2.66(7) (020, 012), 2.56(4) (11), 2.24(5) (12, 102), 2.01(5)(210, 022), 1.707(4) (031), 1.538(4) (032, 004).

Scotlandite occurs as chisel-shaped or bladed crystals elongated along the c-axis, with a tendency to form radiating clusters. The following forms have been determined: {100}, {010}, {011}, {021}, {031}, and {032}. The new mineral has a pronounced cleavage along {100}, and a less good one along {010}. The crystals are pale yellow to greyish-white and colourless, sometimes transparent. Their lustre is adamantine, pearly on cleavage planes.

The mineral is optically biaxial positive, 2Vmeas. 35° 24' (Na). The refractive indices are: α ~ 2.035, β ~ 2.040, and γ ~ 2.085 (Na). Dispersion is strong, v >> r. The extinction is β//b, and α [001] = 20° (γ: [100] = 4°) in the obtuse angle β. H (Mohs) ≤ 2. D = 6.37 and calculated Dx = 6.40 g cm-3.

Scotlandite occurs in cavities in massive baryte and anglesite, and is closely associated with lanarkite and susannite; it represents the latest phase in the crystallization sequence of the associated lead secondary minerals. The label locality of the specimen is the Susanna vein, Leadhills, Scotland.