A variety of mushroom tourmaline from the Kat Chay mine, Momeik, near Mogok, Shan state, Myanmar, consists of a black-to-grey single-crystal core from which a single prismatic crystal reaches to the edge of the mushroom, forming a slight protuberance. The rest of the mushroom (∼50% by volume) consists of extremely acicular sub-parallel crystals that diverge toward the edge of the mushroom. The acicular crystals are dominantly colourless to white, with a continuous black zone (2 mm across) near the edge, and pale pink outside the black zone. The composition varies from ∼Na0.75Ca0.05(Li0.80Al0.70Fe1.10.Mn0.30Ti0.10)Al6Si6(B03)3O18(OH)3(OH,F) at the base of the mushroom to ∼Na0.60Ca0.06(Li1.00Al1.98Fe0.02)Al6(Si5.35B0.65)(BO3)3O18(OH)3(OH,F) close to the edge at the top of the mushroom. The principal substitutions are: (1) YLi + YAl -> yFe* + yFe* and (2) TB + yAl -> Si + yFe*, but there are five other minor substitutions that are also operative. There are six significant compositional discontinuities at textural boundaries in the mushroom, suggesting that the changes in habit are driven in part by changes in external variables such as T and P, plus possible involvement of new fluid phases.

Angastonite, ideally CaMgAl2(PO4)2(OH)4-7H2O, is a newly defined mineral from the Penrice marble quarry, South Australia. The mineral occurs as snow-white crusts and coatings up to ∼1 mm thick associated with minyulite, perhamite, crandallite and apatite-(CaF). The streak is white, the lustre is pearly and the estimated hardness is 2 on the Mohs scale. Angastonite forms platy crystals with the forms {010} (prominent), {101}, {101} and {100} (rare), and also occurs as replacements of an unknown pre-existing mineral. There is one cleavage direction on ﹛010} and no twinning has been observed. Angastonite is triclinic, P1̄, with a = 13.303(1) Å, b = 27.020(2) Å, c = 6.1070(7) Å α = 89.64(1)°, β = 83.44(1)°, γ = 80.444(8)°, V = 2150.5(4) Å3, with Z = 6. The mineral is optically biaxial (+), with refractive indices of α = 1.566(2), β = 1.572(2) and γ 1.584(2) and with 2Vmeas = 70(2)° and 2Vcalc = 71°. Orientation: X ≈ a, Y ≈ b, Z ≈ c; with crystals showing parallel extinction and no axial dispersion. Dmeas is 2.47 g/cm3, whilst Dcalc is 2.332 g/cm3. The strongest four powder-diffraction lines [d in Å, (I/I°), hkl] are: 13.38, (100), 020; 11.05, (25), 11̄0; 5.73, (23), 101, 230 and 111; 8.01, (21), 130. Angastonite is likely to be related to the montgomeryite-group members and have a similar crystal structure, based on slabs of phosphate tetrahedra and Al octahedra.

A Visual Basic program (TOURCOMP) has been written to recast the tourmaline composition into end-member components from electron microprobe data or more complete tourmaline analyses. TOURCOMP is a program based on a linear algebraic model that directly calculates the end-member proportions of tourmalines from their structural formulae. The program is developed for IBM-compatible personal computers running under the Windows™ operating system. The source code has been also translated and compiled in order to run on an Apple computer. Analytical problems, uncertainties concerning site occupancies, and the normalization procedure to determine the structural formula are the main error sources. However, the method of recalculating tourmaline end-members presented in this paper is considered to provide reasonably good results, bearing in mind the chemical complexity of tourmaline.

This work relates the crystal chemistry and the magnetic behaviour of a trioctahedral mica (chemical formula: (K0.90Na0.01Ca0.01Ba0.01 ☐0.07)(Al0.05Fe2+1.10Mg1.38Ti0.32Mn0.01☐0.04)(Al1.12Si2.88)O10 (F0.27OH1.27O0.46); unit cell parameters: a = 5.345(2) Å, b = 9.261(4) Å, c = 20.189(8) Å; β = 95.075(8)°) from Minto Block (Ungava peninsula, northern Quebec, Canada), a region characterized by high magnetic anomalies. Crystallographic and X-ray absorption spectroscopy data suggest a prevalent divalent oxidation state for Fe and a disordered Fe 2+ distribution in the two octahedral sites Ml and M2. The real part of magnetic susceptibility shows two peaks at ∼5.2 K and 120 K. However, as demonstrated by AC magnetic susceptibility measurements, the origin of the two effects is different: the peak position of the first one (i.e. the effect revealed at 5.2 K) is frequency-dependent, thus suggesting a spin-glass like behaviour. The effect at 120 K can instead be attributed to the occurrence of diluted phases in mica matrix, such as Fe oxides.

Aluminium substitution into goethite, α-FeOOH, has been studied systematically by infrared spectroscopy over the frequency interval 150 to 700 cm-1. A range of synthetic compositions. (Fe1-xAlx)OOH, 0 ≤ x ≤ 0.0857, plus end-member diaspore (AlOOH) were examined. The IR spectrum of FeOOH over the range of interest can be deconvoluted into 9 peaks: 670, 633, 497, 451, 409, 396, 360, 290 and 268 cm-1. With addition of Al, the spectra become broader and the frequencies of the modes shift to higher values. An effective line width parameter Δcorr was determined by autocorrelation analysis for each spectrum and there is a significant increase in the Δcorr for compositions with >5.85 mol.% Al substitution, indicating that there is very significant structural strain associated with this solid solution at compositions where a significant number of Al sites will have an additional Al atom in the first cation coordination sphere. Trends in the values of Δcorr with composition mirrored published enthalpy of mixing values indicating that Al-goethite is metastable with respect to the goethite and diaspore end-members. The role of substitutional strain and possible partial order of Al is briefly discussed.

Garnets, omphacite and the minerals of a clinopyroxene/amphibole/plagioclase symplectite in UHP eclogites from Yingshan, Dabieshan have been investigated by TEM and Micro-FTIR. TEM reveals that the predominant microstructures in eclogites and symplectite-forming minerals are chain multiplicity faults (CMFs), dislocation substructures, clusters of water molecules up to ∼50 nm in diameter and recrystallized grains ∼1.75 μm in diameter. This indicates dynamic recrystallization of omphacite, probably during an eclogite-facies metamorphic episode. The deformation structures in symplectite-forming minerals were produced by plastic deformation related to an amphibolite-facies retrograde metamorphic event. CMFs described in the present work demonstrate the existence of an infrequent ½<011> (010) slip system for P2/n omphacite from an UHP eclogite sample from Dabieshan. The frequent occurrence of CMFs in omphacite suggests that they indicate an important deformation mechanism in omphacite and shows that this slip system plays a significant role in the deformation and recovery of eclogite. The hydrous components of deformed minerals may cause plastic deformation of the rocks by dislocation movement and accelerate retrograde metamorphism. Micro-FTIR results show that all the garnets and omphacites contain structural water occurring as hydroxyl groups (OH) or water (H2O). The structural water contents in omphacite range from 110—710 ppm and in garnet from 0—180 ppm. Water released during decompression might supply an early-stage retrograde metamorphic fluid.

A REE-bearing fluorosilicate from the Tommot REE-Nb deposit in Yakutia, Russia, described without a name in 1966, is characterized here as a new species, proshchenkoite-(Y), of the vicanite group of borosilicates. Wavelength-dispersive electron probe analyses gave the following empirical formula: Y3.70REE7.54Ca1.55Na1.16Mn0.77Th0.10Pb0.01)Σ14.83(Fe2+0.83Mn0.15Ti0.02)Σ1.00Ca1.00(P0.70Si0.26As0.04)Σ1.00Si0.26B3.20(O34.55F13.45)Σ48. Boron was analysed with a nuclear microprobe method based on the nuclear reaction 11B(p,α)2α. The simplified formula is (Y,REE,Ca,Mn)15(Fe2+,Mn)Ca(P,Si)Si6B3O34F14. The mineral is trigonal, R3m, with a = 10.7527(7) Å, c = 27.4002(18) Å, V = 2743.6(6) Å 3, Z = 3. The crystal structure was refined to Rl = 0.042 for 1819 observed reflections. Proshchenkoite-(Y) is isostructural with okanoganite-(Y), vicanite-(Ce) and hundholmenite-(Y), and the differences in site occupancies are discussed. The strongest six reflections of the X-ray powder-diffraction pattern [dobs in Å, (I), (hkl)] are: 4.441, (36), (202); 3.144, (77), (214); 3.028, (45). (009); 2.968, (100), (027); 1.782, (32), (330); and 1.713, (32), (1.2.14). The mineral is optically uniaxial (—) with ω 1.734(2) and 8 1.728(2). The Mohs hardness is about 5; density measured on material subject to incipient metamictization is 4.72 g/cm3, as compared to Dcalc = 4.955 g/cm3.

The result of electron microprobe analyses of alleged okanoganite-(Y) from the type locality in Okanogan County, Washington, USA, is also presented. We find here also that P > Si at one of the sites, whereas the analytical data of Boiocchi et al. (2004) indicate Si > P. Consequently, the mineral we have analysed is the P analogue of okanoganite-(Y), another new species.

Coiraite, ideally (Pb,Sn2+)12.5As3Fe2+Sn4+S28, occurs as an economically important tin ore in the large Ag-Sn-Zn polymetallic Pirquitas deposit, Jujuy Province, NW-Argentina. The new mineral species is the As derivative of franckeite and belongs to the cylindrite group of complex Pb sulphosalts with incommensurate composite-layered structures. It is a primary mineral, frequently found in colloform textures, and formed from hydrothermal solutions at low temperature. Associated minerals are franckeite, cylindrite, pyrite-marcasite, as well as minor amounts of hocartite, Ag-rich rhodostannite. arsenopyrite and galena. Laminae of coiraite consist of extremely thin bent platy crystals up to 50 urn long. Electron microprobe analysis (n = 31) gave an empirical formula Pb11.21As2.99Ag0.13Fe1.10Sn6.13S28.0 close to the ideal formula (Pb11.3Sn2+1.2)Σ=12.5As3Fe2+Sn4+S28. Coiraite has two monoclinic sub-cells, Q (pseudotetragonal) and H (pseudohexagonal). Q: a 5.84(1) Å, b 5.86(1) Å, c 17.32(1) Å, β 94.14(1)°, F 590.05(3) Å3, Z = 4, a:b:c = 0.997:1:2.955; H (orthogonal setting): a 6.28(1) Å, b 3.66(1) Å, c 17.33(1) Å, β 91.46(1)°, V398.01(6) Å3, Z = 2, a∶b∶c = 1.716∶1∶4.735. The strongest Debye-Scherrer camera X-ray powder-diffraction lines [d in Å, (I), (hkl)] are: 5.78, (20), (Q and H 003); 4.34, (40), (Q 004); 3.46, (30), (Q and H 005); 3.339, (20), (Q 104); 2.876, (100), (Q and H 006); 2.068, (60), (Q 220).

Felsic volcanic rocks exposed in the Frasnian Gafo Formation, in the Azinhalinho area of Portugal, display very similar geochemical signatures to volcanic rocks from the Iberian Pyrite Belt (IPB). located immediately to the south. The similarities include anomalously low high field-strength elements (HFSE) concentrations, possibly caused by low-temperature crustal melting, which translate into classification problems.

A geochronological study, using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) analyses of zircon grains from these rocks, has provided concordia ages of 356±1.5 Ma and 355±2.5 Ma for two samples of rhyodacite porphyry, and 356±1.4 Ma for a granular rhyodacite. These results show that volcanism at Azinhalinho was broadly contemporaneous with IPB volcanism, widely interpreted as being of Famennian to Visean age. Considering that the host rocks of the Azinhalinho volcanic rocks are Frasnian, and therefore deposited synchronously with the Upper Devonian Phyllite-Quartzite Group sedimentation in the IPB basin, the radiometric ages imply that the Azinhalinho felsic rocks are intrusive and likely represent conduits or feeders to the volcanism of the IPB.

The Silbergrube Aplite (SA) in the Hagendorf-Pleystein Pegmatite District, near Waidhaus, Germany, is a mildly peraluminous NW-SE directed leucogranite dyke. It occurs in association with quartz dykes and aplitic metamorphic mobilizates in the NE Bavarian crystalline basement. The SA differs from other aplitic mobilizates in the region in having a less well developed strain-related mineral orientation and in containing only minor amounts of garnet and tourmaline. The aplitic metamorphic mobilizates and the SA are chemically and mmeralogically almost identical and yield the same age of formation of ∼302 Ma (stage I). The age of formation of the Hagendorf pegmatites seemingly post-dates the emplacement of the SA. The SA was emplaced at the boundary between fine-grained biotite granites and metamorphic country rocks within a zone of structural weakness, favouring the formation of disseminated late magmatic to hydrothermal mineralization of Li-bearing Fe-Mn phosphates (stages II and III). Brittle deformation along this zone was conducive to the faultbound Fe-Mn-Ca phosphates. Mineral telescoping is evident from the presence of Fe2+, Fe3+ and Mn2+ phosphates in fissures and vugs in a texturally highly variable host-rock environment (stage IV). This intimate intergrowth of phosphate minerals reflects contrasting physical and chemical conditions prevailing in a near-surface/ shallow epithermal S-deficient phosphate system (stage IV), similar to what is known from Cu-Au epithermal systems. The most recent mineral assemblages that formed under predominantly oxidizing conditions are correlated with the subtropical weathering during the Neogene which resulted in the formation of a peneplain truncating the SA and its country rocks (stage V). The SA is the root zone of the felsic aplitic-pegmatitic mobilizates in this region and is overprinted by an epithermal phosphate system.