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.

Airborne dust generated by primary blasting was collected in Taffs Well Quarry, just north of Cardiff, Wales. Collections of airborne particulate matter were also made in the nearby village of Morganstown at the same time as the blasting collections. The explosions were recorded on a motor-driven camera and a digital video camera. These images show that the dust clouds generated by the explosions consist of three distinct components; a reddish-grey dust cloud, followed by a light grey dust cloud, and finally a pale grey cloud that stayed near the blast face. It is believed that the reddish-grey cloud was composed mostly of mineral grains, as evidenced by the chiefly red colour of the dolomitic limestone rock in the quarry. The whiter clouds contained more explosive combustion particles (diesel soot). The samples were studied by analytical scanning electron microscopy, very high-resolution field emission scanning electron microscopy, and image analysis. The two different components (minerals and diesel soot) can be readily seen under high-resolution electron microscopy. Any consideration of the possible adverse health effects or nuisance value of this dust needs to consider both of these components. A size distribution of the quarry particles shows that soot particles dominate the assemblage under 2 mm, whereas the mineral grains are more abundant over 2 mm. This contrasts with the Morganstown particle sizes, where the two components show similar size distributions. The determination of the mineralogy of the quarry dust and Morganstown particles has shown highly complex and heterogeneous mixtures, though some distribution patterns are emerging. It is concluded that much of the dust in Morganstown probably originated from sources other than the quarry, such as other local industries, roads and construction sites.

The new mineral species braccoite, ideally NaMn2+5[Si5AsO17(OH)](OH), has been discovered in the Valletta mine dumps, in Maira Valley, Cuneo province, Piedmont, Italy. Its origin is probably related to the reaction between ore minerals and hydrothermal fluids. It occurs as subhedral crystals in brown-red coloured thin masses, with a pale-yellow streak and vitreous to resinous lustre. Braccoite is associated with tiragalloite, for which new data are provided, as well as gamagarite, hematite, manganberzeliite, palenzonaite, quartz, saneroite, tokyoite, unidentified Mn oxides, organic compounds, and Mn arsenates and silicates under study.

Braccoite is biaxial positive with refractive indices α = 1.749(1), β = 1.750(1), γ = 1.760(1). It is triclinic, space group P1̄, with a = 9.7354(4), b = 9.9572(3), c = 9.0657(3) Å, α = 92.691(2), β = 117.057(4), γ = 105.323(3)°, V = 740.37(4) Å3 and Z = 2. Its calculated density is 3.56 g/cm3. The ten strongest diffraction lines of the observed powder X-ray diffraction (XRD) pattern are [d in Å, (I), (hkl)]: 3.055 (69)(22̄1), 3.042 (43)(102), 3.012 (65)(32̄1̄), 2.985 (55)(23̄1̄), 2.825 (100)(213̄), 2.708 (92)(220), 2.627 (43)(23̄2̄), 2.381 (58)(41̄1̄), 2.226 (25)(214̄) and 1.680 (433̄)(36). Chemical analyses by wavelength-dispersive spectroscopy electron microprobe gave (wt.%): Na2O 4.06, CaO 0.05, MnO 41.76, MgO 0.96, Al2O3 0.04, CuO 0.02, SiO239.73, As2O5 6.87, V2O5 1.43, SO3 0.01 and F 0.04. H2O 2.20 was calculated on the basis of 2OH groups p.f.u. Raman spectroscopy confirmed the presence of (SiO4)4–, (AsO4)3– and OH groups. The empirical formula, calculated on the basis of Σ cations-(Na,K) = 11 p.f.u., in agreement with the results of the crystal structure, is Na1.06(Mn2+4.46Mn3+0.32Mg0.19V3+0.01Al0.01Ca0.01)[Si5(As0.48Si0.37V5+0.15)O17(OH)](OH0.98F0.02); the simplified formula is Na(Mn,Mg,Al,Ca)5[Si5(As,V,Si)O17(OH)](OH,F).

Single-crystal XRD allowed the structure to be solved by direct methods and revealed that braccoite is the As-dominant analogue of saneroite. The structure model was refined on the basis of 4389 observed reflections to R1 = 3.47%. Braccoite is named in honour of Dr Roberto Bracco (b. 1959), a systematic minerals collector with a special interest in manganese minerals. The new mineral was approved by the International Mineralogical Association Commission on New Minerals, Nomenclature and Classification (IMA 2013-093).

A new method to measure thermal diffusivity in samples at simultaneous high pressure and high temperature is presented. The sample is placed inside a cylindrical heater and subjected to a heater power that varies sinusoidally with time. The diffusion of the temperature variations into the sample is monitored using radiographic imaging of marker foils. This provides measurements of the phase lag and amplitude variation of the temperature cycle at a range of radii from the sample axis without the need for multiple thermocouples. The technique is tested using a NaCl sample at 4 GPa; the best-fit thermal diffusivity for NaCl at 4 GPa and 673 K is 2.4±0.5x10-6 m2/s.

Amphibole in the lower parts of the Lilloise layered intrusion occurs interstitially and as a replacement of pyroxene; in the upper rocks it is a major cumulus phase. There is an overall trend of increasing Fe/(Fe + Mg) with height. Coupled substitutions which effect the variation in composition of the amphiboles are chiefly Na,K(A)+Al(T) for □A+SiT) and Ti+Al(T) for Fe3+(C)+ Si(T). There is considerable variation in composition both on the specimen scale and within individual grains. This variation, plus scatter found in plots of the coupled substitutions, is partly attributed to many of the amphiboles having replaced pyroxene and also to the effects of magmatic-hydrothermal fluids.

Short-range order in the oxygen co-ordination shell of the Ca ion in a glass of composition Ca3Mg4Al2Si7O24 is investigated by analysis of the extended X-ray absorption fine structure. The estimate of disorder in the short-range oxygen co-ordination is no greater than that for crystalline samples of diopside and bytownite. An estimate of the oxygen environment of calcium in the particular glass is included.

Identification of clinopyroxene lamellae in Bushveld-type orthopyroxene from the Greenhills Ultramafic Complex has been made on the basis of partial analysis by electron microprobe as well as by unit cell determination by prolonged exposure to X-rays of single crystals of orthopyroxene. Lamellae averaging Ca42Mg47Fe11 in composition with an approximate unit cell a 9·79, b 8·90, c 5·29 Å, β 106° 14′, occur in orthopyroxene Ca2Mg67Fe31 with unit cell a 18·28, b 8·85, c 5·20 Å. The Greenhills lamellae are of orientation identical to those described by Hess (1960), which share c and b axes with host orthopyroxene.

Transparent prismatic crystals of Pb2(AsO2OH)Cl2 were collected in black metallurgical slag on the coast in the Punta Zeza area, 3 km south of the town of Lavrion, Greece. Analyses by energy-dispersive X-ray spectrometry (EDS) provided the following chemical composition: PbO 73.04, As2O3 15.97, Cl 11.42, O=Cl –2.58, total 97.85 wt.%. The empirical formula calculated on the basis of As = 1 is HxPb2.03(AsO3)1.00Cl1.995 (x = 0.96). The infrared spectrum of Pb2(AsO2OH)Cl2 has characteristic AsO33– bands at 707 and 594 cm–1, O–H stretching vibrations at 3310 and 2900 cm–1 and a band at 1107 cm–1 which is assigned to As–O–H bending vibrations. The structure, which is monoclinic P21/m, a = 6.4235(8), b = 5.5399(7), c = 9.321(1) Å, β = 90.767(2)°, V = 331.67(7) Å3, R1 = 0.035, is identical to that of synthetic Pb2(AsO2OH)Cl2 and contains two symmetrically unique Pb sites and one As site. The crystal structure is based on [Pb2AsO2OH]2+ double chains interconnected via weak Pb–Cl bonds to produce a three-dimensional framework which is closely related to that of Pb oxysalt minerals containing [O2Pb3]2+ chains of oxocentred [OPb4]6+ tetrahedra including mendipite, damaraite, rickturnerite and plumboselite.

Idiomorphic crystals (up to 3.5 mm) of ferroan platinum, cooperite and mertieite-II were found in a heavy-mineral concentrate from stream sediments of the Darya river in the Aldan Shield, Russia. Pt-Fe crystals display cubic and thin platy habits; occasionally they are twinned. The chemical composition ranges from Pt2.64Fe1.00 to Pt2.88Fe1.00 with Os, Ru, Ir, Rh and Pd below the analytical detection limit of the electron microprobe. X-ray diffractometry of Pt-Fe crystals suggests a F-centred cubic lattice, characteristic of ferroan platinum. Some of the ferroan platinum crystals have large (about 100 μm wide) cooperite overgrowth rims or are covered by a Au-Ag alloy. Cooperite also occurs as large euhedral crystals (up to 3 mm across, partly twinned). Crystals of mertieite-II are speckled with μm-sized (2–5 μm) inclusions of sperrylite and intergrown with minerals of cooperite-braggite solid solution, Pt-Pd-Hg alloy, keithconnite and Au-Ag alloy. Fractures along crystallographic planes of the mertieite-II crystals are filled with Pd-Pt-Fe-Sb-As-Hg-Te-Bi-bearing oxides. The coarse-grained PGM from the Darya have a geological setting similar to the Kondyor PGE placer 75 km to the northeast and are probably related to clinopyroxenite-hornblende-magnetite units of Alaskan-/Uralian-type intrusions.

Viséite is a poorly crystalline mineral which is difficult to study by X-ray diffraction pattern. NMR is a very useful technique to study such poorly crystalline minerals, and 31P, 27Al, and 29Si MAS NMR in conjunction with powder XRD results show that at least our Viséite sample is not a single phase with a structure analogous to that of analcime as previously reported. Rather, it is very disordered with a structure similar to that of crandallite and includes other phases including an undefined aluminophosphate, opal, and a framework aluminosilicate, probably a zeolite. The previously reported variations in the Si content of Viséite are probably due to variable amounts of opal and the framework aluminosilicate.

Several bodies of moderately foliated and porphyroblastic metabasites crop out on the SE side of the metamorphic cover of the Karkonosze granite within metapelites of the Sowia Dolina area (West Sudetes, Saxothuringian zone). Depending on the microstructural setting of the Ca-amphiboles in the rocks, different mineral-chemical trends have been determined for Si, XMg, AlVI, A[Na+K] which serve as semi-quantitative indicators of temperature and pressure changes. Porphyroblasts and prisms oblique to the main foliation in schistose metabasites show zoning from Mg-hornblende and actinolite to tschermakite, and then to Mg-hornblende (or actinolite). Matrix amphiboles and those in pressure shadows around some porphyroblasts have tschermakitic cores and actinolitic rims. Rarely, Ca-amphibole is accompanied in schists by late- to post-tectonic cummingtonite. Thermobarometric calculations involving empirically calibrated amphibole equilibria enable a reconstruction of P-T paths for individual rocks and the unravelling of the metamorphic evolution of the metabasites. Peak metamorphic temperatures of 615–640°C and pressures of 7.3–8.2 kbar were preceded by a variably preserved earlier stage (T = 370–550°C, P = 2.8–6.2 kbar). The final metamorphic episode took place at 450–550°C and 2.5–4.8 kbar and is recorded particularly in rocks close to the Karkonosze pluton. The metabasites shed new light on the history of metamorphism in the Sowia Dolina area. The first two stages of MP-MT metamorphism, coeval with Variscan deformation events (continental collision, burial and subsequent exhumation), took place under epidote-amphibolite then amphibolite facies conditions. The last stage partly concurred with the final stages of Variscan deformation and overlapped the onset of thermal activity associated with the Karkonosze granite. This metamorphic event is documented by metabasites (occasionally cummingtonite-bearing) outcropping close to the granite. Finally, a prehnitebearing assemblage reflects retrograde re-equilibration under greenschist/sub-greenschist facies conditions (T <300–350°C, P <2.5–3 kbar), which might also be partly due to hydrothermal activity around the pluton.

Sodic-calcic and alkali amphiboles from benmoreitic members of the Igaliko Dyke Swarm contain up to 4.13 wt. % ZrO2. It is proposed that Zr enters the amphiboles by a coupled substitution of

(where C = octahedral site and T = tetrahedral site) to produce the richest Zr-bearing amphiboles so far identified, with compositions ranging up to

These amphiboles crystallize at a late stage from magmas which were Zr-rich, highly peralkaline and hydrous, with an fo2 close to the synthetic QMF buffer. The incorporation of Zr in to the amphibole is a consequence of the failure of other Zr-bearing phases (such as zircon, baddeleyite, eudialyte) to crystallize.

Edingtonite and yugawaralite showing sectoral textures were studied by polarized optical microscopy and X-ray analysis. In edingtonite, the m{110} sector (2Vα = 22°) is optically triclinic and the c{001} sector (2Vα = 52°) is orthorhombic. In yugawaralite, the k{011} sector is optically monoclinic, whereas the v{120} sector is triclinic. Their crystal structures were determined. The results of refinement showed that the space groups of the k{011} (Rw = 4.5%) and v{120} (Rw = 5.1%) growth sectors are monoclinic Pc and triclinic P1, respectively. In the v{120} sector, several interatomic distances, bond angles and site occupancies are different with respect to a symmetrical plane of the structure, and therefore the monoclinic c glide is extinct. Thus, the X-ray symmetry correlates with the optical one. From the relationship between the surface and internal texture, the symmetry and sector can be explained by cation (Al/Si) ordering during non-equilibrium crystal growth.

A set of pyribole structures can be derived from a model I-beam containing two distinct silicate chains in which the tetrahedra are rotated by different amounts. The model allows some tetrahedral distortion and is not bound by the parity rule (Thompson, 1970). A subset of pyribole structures which includes all the commonly occurring types can be defined using a new rule: that the structure may contain two types of tetrahedral layer, but no tetrahedral layer may contain two types of tetrahedral chain. This rule is more fundamental than the parity rule and has its origin in the optimization of the edge-to-edge packing of the tetrahedral chains into layers. Pnm21 (amphibole) and Pbc21 (pyroxene) emerge as space groups for ‘low protopyriboles’. The approach used here leads naturally to the − and × -chains notation of Thompson used by Veblen and Burnham (1978).

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.