Penberthycroftite, ideally [Al6(AsO4)3(OH)9(H2O)5]·8H2O, is a new secondary aluminium arsenate mineral from the Penberthy Croft mine, St. Hilary, Cornwall, England, UK. It occurs as tufts of white, ultrathin (sub-micrometre) rectangular laths, with lateral dimensions generally < 20 μm. The laths are flattened on {010} and elongated on [100]. The mineral is associated with arsenopyrite, bettertonite, bulachite, cassiterite, chalcopyrite, chamosite, goethite, liskeardite, pharmacoalumite–pharmacosiderite and quartz. Penberthycroftite is translucent with a white streak and a vitreous to pearly lustre. The calculated density is 2.18 g/cm3. Optically, only the lower and upper refractive indices could be measured, 1.520(1) and 1.532(1) respectively. No pleochroism was observed. Electron microprobe analyses (average of 14) with H2O obtained from thermogravimetric analysis and analyses normalized to 100% gave Al2O3 = 31.3, Fe2O3 = 0.35, As2O5 = 34.1, SO3 = 2.15 and H2O = 32.1. The empirical formula, based on nine metal atoms and 26 framework anions is [Al5.96Fe0.04(As0.97Al0.03O4)3(SO4)0.26(OH)8.30(H2O)5.44](H2O)7.8, corresponding to the ideal formula [Al6(AsO4)3(OH)9(H2O)5]·8H2O. Penberthycroftite is monoclinic, space group P21/c with unit-cell dimensions (100 K): a = 7.753(2) Å, b = 24.679(5) Å, c = 15.679(3) Å and β = 94.19(3)°. The strongest lines in the powder X-ray diffraction pattern are [dobs in Å(I) (hkl)] 13.264(46) (011); 12.402(16)(020); 9.732(100)(021); 7.420(28)(110); 5.670(8)(130); 5.423(6)(1̄31). The structure of penberthycroftite was solved using synchrotron single-crystal diffraction data and refined to wRobs = 0.059 for 1639 observed (I> 3σ(I)) reflections. Penberthycroftite has a heteropolyhedral layer structure, with the layers parallel to {010}. The layers are strongly undulating and their stacking produces large channels along [100] that are filled with water molecules. The layers are identical to those in bettertonite, but they are displaced relative to one another along [001] and [010] such that the interlayer volume is decreased markedly (by ∼10%)relative to that in bettertonite, with a corresponding reduction in the interlayer water content from 11 H2O per formula unit (pfu) in bettertonite to 8 H2O pfu in penberthycroftite.

Crimsonite (IMA2014-095), PbFe3+2(PO 4)2(OH)2, the phosphate analogue of carminite, is a new mineral from the Silver Coin mine, Valmy, Iron Point district, Humboldt County, Nevada, USA, where it occurs as a low-temperature secondary mineral in association with fluorwavellite, goethite, hematite, hentschelite, plumbogummite and variscite on quartz. Crimsonite occurs in subparallel aggregates of deep red blades or plates flattened on {100} and up to 0.1 mm in maximum dimension. The streak is light purplish orange. Crystals are transparent and have adamantine lustre. The Mohs hardness is ∼3½, the tenacity is brittle, the fracture is irregular to splintery and an imperfect cleavage is likely on {101}. The calculated density is 5.180 g/cm3. Crimsonite is optically biaxial (+), with 2V = 85.5(5)° and γ – α = 0.011. Using the Gladstone-Dale relationship, the calculated indices of refraction are α = 2.021, β = 2.026 and γ = 2.032. The optical orientation is X = b; Y = a; Z = c and the pleochroism is X light orange, Y light yellow, Z red brown; Y < X < Z. Electron microprobe analyses provided PbO 40.69, CaO 0.60, ZnO 0.72, CuO 0.13, Fe2O3 23.36, Al2O3 0.34, V2O5 0.70, As2O5 12.05, P2O5 16.03, SO3 0.33 and H2O 3.64 (structure), total 98.59 wt.%. The empirical formula (based on 10 O apfu) is (Pb1.06Ca0.06)∑1.12(Fe1.71Zn0.05Al0.04Cu0.01)∑1.81(P1.32As0.61V0.05S0.02)∑2.00O8[(OH)1.64(H2O)0.36]∑2.00. Crimsonite is orthorhombic, Cccm, a = 16.2535(13), b = 7.4724(4), c = 12.1533(9) Å, V = 1476.04(17) Å3 and Z = 8. The eight strongest lines in the powder X-ray diffraction pattern are [dobs in Å(I)(hkl)]: 5.86(42)(111); 4.53(45)(112); 3.485(64)(113); 3.190(100) (022); 3.026(40)(004); 2.902(54)(511); 2.502(77)(422) and 2.268(54)(224). The structure of crimsonite (R1 = 3.57% for 740 Fo > 4σF) contains FeO6 octahedra that share edges to form dimers, which are then linked to other dimers by corner sharing to form chains along [010]. These chains are linked by PO4 tetrahedra yielding sheets parallel to {001}. The sheets are linked to one another via bonds to 8-coordinated Pb2+ atoms with non-stereoactive 6s2 lone-electron pairs.

The Usambara effect, i.e. a change of tourmaline colour from deep-green to dark-red with increasing path length of light, has been studied by optical absorption spectroscopy and colourimetric calculations on a sample of Tanzanian tourmaline of predominant dravite composition with 0.12 apfu Cr. For comparison a dark-green vanadium-bearing tourmaline from Tanzania (0.05 apfu V), which does not show such an effect, was also investigated. As established, the Usambara effect, by its nature, is closely related to the alexandrite effect, although in this case the colour change is not caused by change of spectral composition of the light of illumination, but by spectral positions of the spin-allowed absorption bands of Cr3+, a specific ratio of light transmission in two windows of transparency, green and red, and by non-linear, exponential dependence of the light transmittance on the thickness of sample. A threshold chromium content must be exceeded for the Usambara effect to show, that is, sufficient chromium for there to be two deep and well-demarcated windows of transparency in the visible range. The overall colouration results from mixing of two additive colours coming through the windows of transparency. A dark-green chromium-bearing tourmaline from the Ural Mountains (0.40 and 0.20 apfu Cr and Fe, respectively) shows how admixtures of other chromophore ions, namely, Fe2+ and Fe3+, can suppress the Usambara effect in tourmaline.

Relative to its extremely low abundance in the Earth's crust, tellurium is the most mineralogically diverse chemical element, with over 160 mineral species known that contain essential Te, many of them with unique crystal structures. We review the crystal structures of 703 tellurium oxysalts for which good refinements exist, including 55 that are known to occur as minerals. The dataset is restricted to compounds where oxygen is the only ligand that is strongly bound to Te, but most of the Periodic Table is represented in the compounds that are reviewed. The dataset contains 375 structures that contain only Te4+ cations and 302 with only Te6+, with 26 of the compounds containing Te in both valence states. Te6+ was almost exclusively in rather regular octahedral coordination by oxygen ligands, with only two instances each of 4- and 5-coordination. Conversely, the lone-pair cation Te4+ displayed irregular coordination, with a broad range of coordination numbers and bond distances. A threshold was applied for Te4+–O links of ∼2.45 Å or 0.3 valence units with some flexibility, as a criterion to define strongly bound Te–O polymers and larger structural units. Using this criterion, Te4+ cations display one-sided 3-, 4- or 5-coordination by oxygen (with rare examples of coordination numbers 2 and 6). For both valence states of Te, examples are known of TemOn complexes which are monomeric (m = 1; neso), noncyclic finite oligomers (soro), rings (cyclo), infinite chains (ino), layers (phyllo) and frameworks (tecto tellurates). There is a clear analogy to the polymerization classes that are known for silicate anions, but the behaviour of Te is much richer than that of Si for several reasons: (1) the existence of two cationic valence states for Te; (2) the occurrence of multiple coordination numbers; (3) the possibility of edge-sharing by TeOn polyhedra; (4) the possibility for oxygen ligands to be 3-coordinated by Te; and (5) the occurrence of TemOn polymers that are cationic, as well as neutral or anionic. While most compounds contain only one or two symmetrically distinct types of Te atom, Pauling's Fifth Rule is frequently violated, and stoichiometrically simple compounds such as CaTeO3 can have polymorphs with up to 18 distinct Te sites. There is a tendency for local symmetry features such as the threefold axis of a TeO6 octahedron or the acentric symmetry of a Te4+On polyhedron to be inherited by the host structure; the latter in particular can lead to useful physical properties such as nonlinear optical behaviour. We develop for the first time a hierarchical taxonomy of Te-oxysalt structures, based upon (1) valence state of Te; (2) polymerization state of TemOn complexes; (3) polymerization state of larger strongly-bound structural units that include non-Te cations. Structures are readily located and compared within this classification.

The rare potassium zirconium silicate dalyite has been identified for the first time on Terceira, Azores, within syenitic ejecta of the Caldeira-Castelinho Ignimbrite Formation. New quantitative analyses of this dalyite were combined with the small number of published analyses from various locations worldwide to evaluate the mineral's compositional variability. Additionally, solid-state modelling has been applied to assess the site allocations of substituting elements. The new analyses yield the average formula (K1.84Na0.15)∑=1.99(Zr0.94Ti0.012Hf0.011Fe0.004)∑=0.967Si6.03O15. Model results predict the placement of substituting Hf and Ti in the octahedral site, and highlight the overall complexity in the incorporation of Fe, Mg and Ba. The combined dataset reveals that dalyite found within peralkaline granites and syenites is generally defined by higher Na↔K substitution and lower Ti↔Zr substitution relative to dalyite from highly potassic rocks. The Terceira dalyite exhibits a bimodal variation in the degree of Na↔K substitution which is attributed to a K-enrichment trend induced by late-stage pore wall crystallization and albitization, coupled with the control of pore size upon the degree of supersaturation required to initiate nucleation of dalyite in pores of varying size.

The Proterozoic Sushina Hill Complex is the only agpaitic complex, reported from India and is characterized by a eudialyte-rinkite-bearing nepheline syenite. The complex is considered a ‘metamorphosed agpaitic complex'. This study describes the mineral assemblages formed during successive stages of evolution from magmatic to hydrothermal stages and low-temperature subsolidus re-equilibration assemblage. The primary-late magmatic assemblage is characterized by albite, orthoclase, unaltered nepheline, zoned diopside-hedenbergite, rinkite, late magmatic eudialyte and magnesio-arfvedsonite formed at ∼700°C with maximum aSiO2 of 0.60. In contrast, a deuteric assemblage (400-348°C) is represented by aegirine-jadeite-rich clinopyroxene, post-magmatic eudialyte, sodalite, analcime and the decomposition assemblages formed after eudialyte with decreasing aSiO2 (0.52-0.48). A further low-temperature subsolidus assemblage (≤250°C) represented by late-forming natrolite could be either related to regressive stages of metamorphism or a continuum of the subsolidus processes. Considering the P/T range of the greenschist - lower-amphibolite facies of metamorphism it is evident that the incorporation of a jadeite component within pyroxene is related to a subsolidus process between ∼400°C and 348°C in a silica deficient environment. We emphasize that the deuteric fluid itself acted as an agent of metamorphism and the decomposition assemblage formed after eudialyte is retained even after metamorphism due to the convergence of subsolidus and metamorphic domains. The formation of jadeite-rich aegirine is not considered to result from metamorphism. Overall it is near-impossible to discern any bona fide metamorphic textures or mineral assemblages in these syenites which appear to preserve a relict mineralogy regardless of their occurrence in country rocks which have experienced greenschist - amphibolite facies metamorphism. The Sushina complex is very similar in this respect to the Norra Kärr complex (Sweden).

Optical microscopy, Raman spectroscopy and electron probe microanalyses were conducted on a migmatitic metapelite to investigate the effects of alpha radiation and subsequent alteration at the interface between uraninite inclusions and the host minerals biotite, chlorite and albitic plagioclase. The study reveals (1) anomalous colouration under the polarizing microscope; (2) pertinent changes in the characteristic Raman spectra of host phases; (3) reaction aureoles, composed of secondary phases (viz. chlorite and K-feldspar) of various sizes (∼15–45 μm) within biotite and plagioclase, respectively; (iv) K-feldspatization and sericitization of plagioclase at the grain boundaries; (5) agreement between the observed α-penetration depths and the Monte-Carlo simulation results; and (6) dissolution textures within the matrix monazites. Analysis of the compositions of the reaction aureoles in albitic plagioclase reveals a systematic distribution of K-feldspar-, LREE- and clay-rich zones; while the same in biotite is composed of secondary chlorite. The growth sequence of the secondary phases indicates an influx of a K-rich fluid, following intense radiation damage, efficiently superimposed by LREE-metasomatism and later acidic alteration. These changes took place under low-temperature (≤150°C) conditions, wherein radial cracks (within plagioclase) and cleavages/fractures (within biotite) favoured fluid infiltration-circulation into the reaction aureoles. Depletion of the LREEs from the dissolved matrix monazites and their enrichment as a discrete LREE phase within the damaged aureoles in plagioclase demonstrate micrometre-scale LREE mobility.

The layered agpaitic nepheline syenites (kakortokites) of the Ilímaussaq complex, South Greenland, host voluminous accumulations of eudialyte-group minerals (EGM). These complex Na-Ca-zirconosilicates contain economically attractive levels of Zr, Nb and rare-earth elements (REE), but have commonly undergone extensive autometasomatic/hydrothermal alteration to a variety of secondary mineral assemblages. Three EGM alteration assemblages are recognized, characterized by the secondary zirconosilicates catapleiite, zircon and gittinsite. Theoretical petrogenetic grid models are constructed to assess mineral stabilities in terms of component activities in the late-stage melts and fluids. Widespread alteration of EGM to catapleiite records an overall increase in water activity, and reflects interaction of EGM with late-magmatic Na-, Cl- and F-rich aqueous fluids at the final stages of kakortokite crystallization. Localized alteration of EGM and catapleiite to the rare Ca-Zr silicate gittinsite, previously unidentified at Ilímaussaq, requires an increase in CaO activity and suggests post-magmatic interaction with Ca-Sr bearing aqueous fluids. The pseudomorphic replacement of EGM in the kakortokites was not found to be associated with significant remobilization of the primary Zr, Nb and REE mineralization, regardless of the high concentrations of potential transporting ligands such as F and Cl. We infer that the immobile behaviour essentially reflects the neutral to basic character of the late-magmatic fluids, in which REE-F compounds are insoluble and remobilization of REE as Cl complexes is inhibited by precipitation of nacareniobsite-(Ce) and various Ca-REE silicates. A subsequent decrease in F– activity would furthermore restrict the mobility of Zr as hydroxyl-fluoride complexes, and promote precipitation of the secondary zirconosilicates within the confines of the replaced EGM domains.

Many layered intrusions are considered to have been repeatedly inflated by magma additions, but rates of magma mixing relative to rates of layer accumulation are difficult to model. The nature of magma recharge through the interval including the Pyroxenite Marker (PM), Main Zone, Bushveld Complex, South Africa, is examined with regard to such processes. The plagioclase compositions (An value) in five previously published and three new profiles (presented here and focusing on the core compositions) that are at least 600 m in vertical extent and spread along a strike length of 110 km are evaluated. The compilation of the eight profiles shows the following trends. Upward reversals in compositions show considerable lateral as well as vertical variations. Lateral variations show a range in: (1) the minimum An value reached in each profile prior to the onset of magma recharge (An51 to An59); (2) the depth below the PM at which the minimum value is observed (50 to 575 m); (3) the An value close to the PM (An54 to An75); (4) the maximum value recorded above the PM (An63 to An76); (5) the height above the PM at which this maximum value is reached (0 to 300 m) – in all cases, the highest values of An occur at the northern end of the studied sections; and (6) the vertical extents over which the reversals occur range from 150 to over 600 m indicating very protracted magma additions and/or slow mixing. The PM terminates toward the south, and close to this termination the immediate footwall rocks to the PM change from north to south from gabbronorite to magnetite gabbronorite. A cross-section through these profiles defines two basins, with an intervening structural upwarp. The magma pulses that were added to produce very gradual and protracted reversals in mineral compositions through the PM interval ponded initially at the base of the northern basin, and did not homogenize the entire magma column. These added magmas did not overflow and have an effect on mineral compositions in the southern basin until after considerable replenishment and crystallization (including the PM) had taken place in the northern basin. We emphasize the prolonged period(s) of magma input and slow rate of vertical homogenization of the magma column during the formation of this sequence of as much as 400 m of the Main Zone.

The crystal chemistry of allactite from Långban, Värmland (Sweden) was investigated by single-crystal X-ray and neutron diffraction, optical absorption spectroscopy, Fourier-transform infra-red spectroscopy (FTIR) and electron microprobe analysis by wavelength-dispersive spectroscopy (EPMA-WDS). The optical spectra indicate the presence of Mn in valence state 2+ only. Assuming 16 O atoms per formula unit, arsenic as As5+ and the (OH) content calculated by charge balance, the resulting formula based on the EPMA-WDS data is (Mn2+ 6.73Ca0.13Mg0.12Zn0.02)∑7.00(As5+)2.00O16H8, very close to the ideal composition Mn7(AsO4)2(OH)8. In the unpolarized FTIR spectrum of allactite, fundamental (OH)-stretching bands are observed at 3236, 3288, 3387, 3446, 3484, 3562 and 3570 cm–1, suggesting that a number of OH environments, with different hydrogen bond strengths, occur in the structure. The neutron structure refinement shows that four independent H sites occur in allactite with full site occupancy, all as members of hydroxyl groups. The complex hydrogen-bonding scheme in the allactite structure is now well defined, with at least nine hydrogen bonds energetically favourable with mono-, bi- and trifurcated configurations.

Iron-cross twins of pyrite are well known among mineralogists, however it is quite surprising that the conditions of their formation remain unexplored. To address this question we studied pyrite twins from the Upper Permian silts of Mt. Katarina near Ljubljana (Slovenia), which represent one of the most typical geological environments for twinned pyrite. Mineralization of pyrite starts with a reduction of the primary red-coloured hematite-rich sediment by sulfide-rich fluids that penetrated the strata. A short period of magnetite crystallization is observed prior to pyrite crystallization, which indicates a gradual reduction process. Sulfur isotope analysis of pyrite shows an enrichment in δ34S, suggesting its origin from the neighbouring red-bed deposit. Other sulfides, such as chalcopyrite and galena, formed at the end of pyrite crystallization. Remnants of mineralizing fluids trapped at the interfaces between the inclusions and host pyrite show trace amounts of Pb and Cu, indicating their presence in the solutions throughout the period of pyrite crystallization. An electron microscopy and spectroscopy study of twin boundaries showed that interpenetration twinning is accomplished through a complex 3D intergrowth of primary {110} Cu-rich twin boundaries, and secondary {100} boundaries that are pure. We show that approximately one monolayer of Cu atoms is necessary to stabilize the {110} twin structure. When the source of Cu is interrupted, the two crystal domains continue to form {100} interfaces, that are more favourable for pure pyrite.

Moskvinite-(Y), Na2K(Y,REE)Si6O15, is a rare mineral, which until now has only been described from its type locality Dara-i-Pioz, Tajikistan. At Ilímaussaq moskvinite-(Y) was discovered in a drill core from Kvanefjeld, where it occurs as a replacement mineral associated with a mineral belonging to the britholite group. The composition was determined by a combination of electron probe microanalysis and laser ablation inductively coupled plasma mass spectrometry analyses. The empirical formula based on 15 oxygens is Na1.94K0.99(Y0.94Yb0.03Er0.03 Dy0.03Ho0.01Gd0.01) ∑1.05Si5.98O15. The coexistence of an almost pure Y and a light rare-earth element (REE) mineral is interpreted as fractionation of REE and Y during the replacement of an earlier formed REE mineral. Theoretical calculations of the observed replacement of feldspathoids by natrolite show that the generated fluid would have pH > 8, which inhibits large scale mobility of REE. In addition, a K-Fe sulfide member of the chlorbartonite-bartonite group is for the first time observed in Ilímaussaq where it occurs where sodalite is replaced by natrolite and arfvedsonite by aegirine. The sulfide incorporates the S and some of the Cl generated by the alteration of sodalite, whereas the K and Fe originates from the replacement of arfvedsonite by aegirine.

Berezanskite, ideally Ti□2KLi3(Si12O30), is hexagonal, space group P6/mcc, a = 9.898(4), c = 14.276(6) Å, V = 1211.2(9) Å3, Z = 2. The crystal structure was refined to an R1 index of 2.08% based on 392 unique observed reflections. Berezanskite is isostructural with milarite, ideally ACa2BoCKT(2)(Be2Al)(T(1)Si12O30)(H2O)0–2. The structural unit is of the form [T(2)3T(1)12O30] with T(1) = Si and T(2) = Li, in which (LiO4) tetrahedra link [Si12O30] six-membered double-rings into a framework. The A, B and C sites occur in the interstices of the framework with the following site populations: A = Ti4+2, <A–O>= 1.938(2) Å; B =□2; C = K, <C–O> = 3.058(2) Å. In the T(2) = Li3 milarite-group minerals, the <C–O> distance is inversely related to the occupancy of the B site.

A crystallographic and chemical study of two 'elsmoreite' samples (previously described as 'ferritungstite') from the Hemerdon mine (now known as the Drakelands mine), Devon, United Kingdom has shown them to be two different polytypes of hydrokenoelsmoreite. Hydrokenoelsmoreite-3C(HKE-3C) crystallizes in space group , with the unit-cell parameter a = 10.3065(3) Å. Hydrokenoelsmoreite-6R (HKE-6R) crystallizes in space group , with the unit-cell parameters a = 7.2882(2) Å and c = 35.7056(14)Å. Chemical analyses showed that both polytypes have Na and Fe/Al substitution giving the formulae: (Na0.28Ca0.04K0.02(H2O)0.20⁏1.46)∑2.00(W1.47Fe3+0.32Al0.21As5+0.01)∑2.00[O4.79(OH)1.21]∑6.00·(H2O)(3C) and (Na0.24Ca0.04K0.03(H2O)0.63⁏1.06)∑2.00(W1.42Fe3+0.49Al0.08As5+0.01)∑2.00[O4.65(OH)1.35]∑6.00·(H2O)(6R). The doubling of the unit cell in the 6R phase is due to ordering of Na and ( ,H2O) in the A site; no long-range ordering is observed between W and Fe/Al in the B site.

Pauladamsite (IMA2015-005), Cu4(SeO3)(SO4)(OH)4·2H2O, is a new mineral from the Santa Rosa mine, Darwin district, Inyo County, California, USA, where it occurs as a secondary oxidation-zone mineral in association with brochantite, chalcanthite, gypsum, ktenasite, mimetite, schulenbergite and smithsonite on limonitic gossan. Pauladamsite forms green, multiply twinned blades up to 0.5 mm long grouped in radial sprays. The streak is pale green. Crystals are transparent and have vitreous to silky lustre. The Mohs hardness is ∼2, the tenacity is brittle, the fracture is irregular and crystals exhibit one perfect cleavage on [001]. The calculated density is 3.535 g/cm3. Electron microprobe analyses provided: CuO 48.96, ZnO 3.56, SeO2 18.82, SO3 13.90, H2O 13.29 (calc.), total 98.53 wt.%. The empirical formula (based on 13 O apfu) is: (Cu3.55Zn0.25)∑3.80Se0.98SO13H8.50. Pauladamsite is triclinic, P1, a = 6.0742(7), b = 8.4147(11), c = 10.7798 (15) Å, α = 103.665(7), β = 95.224(7), γ = 90.004(6)°, V = 533.03(12) Å3 and Z = 2. The eight strongest lines in the powder X-ray diffraction pattern are [dobs in Å(I)(hkl)]: 10.5(46)(011); 3.245(100)(001); 5.81(50)(011); 2.743(49)(112); 3.994(67)(012); 3.431(23)(1̄12,1̄2̄1,1̄20); 2.692(57)(03̄2,1̄22,2̄1̄2); and 2.485(39)(21̄2,1̄3̄2,02̄4). The structure of pauladamsite (R1 = 10.6% for 2086 Fo > 4σF) contains Cu2+O6 octahedra, SO4 tetrahedra and Se4+O3 pyramids. There are four different CuO6 octahedra, each of which exhibits typical Jahn-Teller distortion, with four short equatorial Cu–O bonds and two much longer apical Cu–O bonds. The CuO6 octahedra share edges to form five-octahedra-wide bands extending along [100]. Adjacent bands are connected in the [011̄] direction by bridging SO4 tetrahedra and in the [011] direction by bridging Se4+O3 pyramids, thereby forming a framework.

The geology of the 2.7 Ga Stillwater Complex in South-Central Montana is reviewed with a focus on the role of volatiles in locally modifying both the crystallization sequence of the evolving parent magma and the initially precipitated solid assemblages to favour olivine ± chromite. A secondary origin for these two minerals is particularly probable for the olivine-bearing rocks of the Banded series and, at a minimum, also increasing their modal abundance in the Peridotite zone of the Ultramafic series. Direct evidence for volatiles includes the presence of high-temperature fluid inclusions in pegmatoids and hydrous melt inclusions (now crystallized) in chromite and olivine from both the Ultramafic and the Banded series rocks. Indirect evidence includes the boninitic character of the parent magma, the presence of volatile-bearing minerals including high-temperature carbonates, rock textures, and Cl / F variations in apatite. Mechanisms which favour the formation of olivine (± chromite) over pyroxene include volatile phase boundary shifts induced by added H2O, incongruent melting of pyroxene by hydration of a partly-molten mush, and the near- to sub-solidus replacement of pyroxene by olivine and chromite by silica-undersaturated fluids. These mechanisms cast doubt that magmas with different liquid lines of descent were involved in the crystallization of the Stillwater Complex. A dry Stillwater magma would have been mineralogically and modally much less varied and lacking in high-grade platinum-group element and chromium deposits.

Two novel copper selenite chlorides, K[Cu3O](SeO3)2Cl (I) and Na2[Cu7O2](SeO3)4Cl4 (II), have been synthesized by the CVT method. Their crystal structures have been solved by direct methods and refined by least-squares techniques. I is triclinic, space group P1̄, a = 7.6821(5), b = 8.1179(5), c = 8.7836(6) Å, α = 113.193(3), β = 108.735(4), γ = 98.245(4)°, V = 453.32(5) Å3, R1 = 0.0481 for 1210 unique reflections with F≥4σ(F); II is triclinic, space group P1̄,a = 7.4362(6), b = 8.3361(7), c = 9.1343(11) Å,α = 110.277(6), β = 106.212(6), γ = 105.158(4)°, V = 467.94(8) Å3, R1 = 0.0265 for 2498 unique reflections with F≥4σ(F). The structures of I and II can be described in terms of dimers of copper oxocentred tetrahedra. In I, two (OCu4)6+ tetrahedra share a common Cu···Cu edge to form the [O2Cu6]8+ dimer, whereas the structure of II is based upon two (OCu4)6+ tetrahedra linked together by one common Cu atom resulting in the formation of the [O2Cu7]10+ dimer. A comparison with related minerals and inorganic compounds is given.

Rare-earth elements (REE) are viewed as 'critical metals' due to a complex array of production and political issues, most notably a near monopoly in supply from China. Red mud, the waste product of the Bayer process that produces alumina from bauxite, represents a potential secondary resource of REE. Karst bauxite deposits represent the ideal source material for REE-enriched red mud as the conditions during formation of the bauxite allow for the retention of REE. The REE pass through the Bayer Process and are concentrated in the waste material. Millions of tonnes of red mud are currently stockpiled in onshore storage facilities across Europe, representing a potential REE resource. Red mud from two case study sites, one in Greece and the other in Turkey, has been found to contain an average of ∼1000 ppm total REE, with an enrichment of light over heavy REE. Although this is relatively low grade when compared with typical primary REE deposits (Mountain Pass and Mount Weld up to 80,000 ppm), it is of interest because of the large volumes available, the cost benefits of reprocessing waste, and the low proportion of contained radioactive elements. This work shows that ∼12,000 tonnes of REE exist in red mud at the two case study areas alone, with much larger resources existing across Europe as a whole.