Mackinawite, tetragonal FeS, has been synthesised by reacting iron with Na2S solutions. A Rietveld structure refinement of X-ray powder diffraction data, recorded using X-rays monochromated from synchrotron radiation with a wavelength of 0.6023 Å, has been performed. The structure has been refined in the tetragonal space group, P4/nmm, and has the following cell parameters: a = 3.6735(4), c = 5.0328(7) Å, V = 67.914(24) Å3. Our refinement shows that the FeS4 tetrahedron in mackinawite is almost perfectly regular, with a much smaller distortion than has been previously reported. An improved X-ray diffraction data set is provided.

A design for a micro furnace and a fusion technique are described by which silicate materials (in particular picritic and peridotitic rock compositions) may be fused and quenched to a homogeneous glass without significant loss of components, for the purposes of bulk analysis. The furnace consists of a Pt wire electrical resistance heater mounted in a furnace assembly which is fitted to a microscope stage. Microscopic examination of the sample during the fusion process allows the sample to be quenched as soon as all crystalline material has been fused and thus minimizes the loss of iron and alkalis due either to over-heating or prolonged fusion time. Analysis of glass beads of a model peridotite composition (analysed independently by X-ray fluorescence analysis) shows that for typical fusion times (5–10 seconds) the bulk composition is preserved at distances of > 25 µm from the margins of the glass beads. Analysis of natural rock powders of known composition shows that the method can be used to analyse whole rock compositions. The furnace is simple to construct and cheap to run and provides a simple and rapid method of producing glass samples for bulk analysis.

Detailed microprobe and modal data for a sample of layered, garnetiferous, quartzose paragneiss reveal significant differences in garnet-biotite Mg-Fe distribution coefficients (Kd) — and hence paleotemperatures — determined for leucocratic (modal Grt+Bt<25 vol.%) and mesocratic (Grt+Bt> 25 vol.%) layers. In leucocratic layers, lnKd determined from both the core and rim compositions of minerals shows a range of values that varies sympathetically with the absolute amount of garnet and biotite, and, as demonstrated in other studies, inversely with the distance separating both minerals. Due to the small size (<2 mm) of garnets, which facilitated diffusional re-equilibration during cooling from peak metamorphic temperature, lnKd does not correlate to modal Bt/Grt ratios. The largest garnets, which occur in mesocratic layers, nonetheless tend to preserve the most pronounced (retrograde) zoning patterns (i.e. rimward increase in Fe/Mg), consequently mineral core composition lnKd values correlate with grain diameter except where garnets contain abundant biotite inclusions. The highest Grt-Bt temperatures (∼700°C are recorded by: (1) the composition of relatively widely-separated (>0.3 mm) grains in highly leucocratic layers; and (2) the core compositions of relatively large (>1 mm), inclusion-free grains in mesocratic layers. More closely spaced garnets and biotites in leucocratic layers, and small grains in mesocratic layers, give a range of temperatures intermediate between Tmax and diffusional blocking temperatures (∼ 560°C) recorded by the rim compositions of contiguous grains.

Morimotoite, Ca3TiFe2+Si3O12, has been found in contaminated rocks which are considered to be a kind of endoskarn at Fuka, Bitchu-Cho, Okayama Prefecture, Japan. Morimotoite is derived from andradite, , by the substitution Ti + Fe2+ = 2Fe3+. It is associated with calcite, vesuvianite, grossular, wollastonite, hematite, prehnite, fluorapatite, perovskite, zircon, baddeleyite and calzirtite. It is cubic with space group Ia3d. The unit cell dimension a is 12.162(3) Å. Its refractive index n is 1.995(2) and the density 3.75(2) g cm−3 (meas.), 3.80 g cm−3 (calc.). The Mohs' hardness is 7.5. Calculation of the analytical data on the basis of twelve oxygen atoms and eight cations shows that this mineral has a simplified chemical formula Ca3(Ti,Fe2+Fe3+)2(Si,Fe3+)3O12 where Ti > Fe2+ > 0.5. Morimotoite was synthesized at low oxygen fugacities, 650 and 700°C and 1 kbar total pressure.

Scanning Electron Microscopy and Transmission Electron Microscopy show that normal, slightly turbid alkali feldspars from many plutonic rocks contain high concentrations of micropores, from ∼1 µm to a few nm in length, typically 0.1 µm. There may be 109 pores mm−3 and porosities as high as 4.75 vol.% have been observed, although ∼1% is typical. Only ‘pristine’ feldspars, which are dark coloured when seen in the massive rock, such as in larvikite and some rapakivi granites, are almost devoid of pores. Weathering enlarges prexisting pores and exploits sub-regularly spaced edge dislocations which occur in semicoherent microperthites, but the underlying textures which lead to skeletal grains in soils are inherited from the high temperature protolith. Most pores are devoid of solid inclusions, but a variety of solid particles has been found. Although the presence of fluid in pores cannot usually be demonstrated directly, crushing experiments have shown that Ar and halogens reside in fluids. Some pores are ‘negative crystals’, often with re-entrants defined by the {110} Adularia habit, while others have curved surfaces often tapering to thin, cusp-shaped apices. The variable shape of pores accounts for the ability of some pores to retain fluid although the texture is elsewhere micropermeable, as shown by 18O exchange experiments.

Apart from rare, primary pores in pristine feldspar, pore development is accompanied by profound recrystallization of the surrounding microtexture, with partial loss of coherency in cryptoperthites. This leads to marked ‘deuteric coarsening’ forming patch and vein perthite, and replacement of ‘tweed’ orthoclase by twinned microcline. The Ab- and Or-rich phases in patch perthite are made up of discrete subgrains and the cuspate pores often develop at triple-junctions between them. Coarsened lamellar and vein perthites are composed of microporous subgrain textures. These ‘unzipping’ reactions result from fluid-feldspar interactions, at T <450°C in hypersolvus syenites and T < 350°C in a subsolvus granites, and are driven by elastic strain-energy in coherent cryptoperthites and in tweed textures. Further textural change may continue to surface temperatures. In salic igneous rocks there is a general connection between turbidity and the type of mafic mineral present; pristine alkali feldspars occur in salic igneous rocks with a preponderance of anhydrous mafic phases.

Because alkali feldspar is so abundant (and larger, 10 μm pores have previously been described in plagioclase), intracrystal porosity is a non-trivial feature of a large volume of the middle and upper crust. The importance of pores in the following fields is discussed: 39Ar/40Ar dating and ‘thermochronometry’; oxygen exchange; Rb and Sr diffusion; weathering; experimental low-temperature dissolution; development of secondary porosity and diagenetic albitization; leachable sources of metals; nuclear waste isolation; deformation; seismic anisotropy; electrical conductivity. Important questions concern the temperature range of the development of the textures and their stability during burial and transport into the deeper crust.

PEEM allows ‘real-time’ observations to be made of solid-state transformations and other high-temperature processes taking place during vacuum-heating up to c. 2000°C The solid state transformations of an amphibole-rich hornblendite specimen have been observed in the temperature range of 750–1000°C (± 50°C Between c. 970–990°C a rapid change in orientation contrast was observed, indicating a structural rearrangement from an oxyhornblende crystal lattice to a clinopyroxene structure. This phase retains the original amphibole shape and texture (including two 120°C intersecting cleavage traces), but possesses a clinopyroxene crystal structure. At higher temperatures this phase is seen to decompose, forming iron oxides and other fine-grained products. PEEM has provided useful information on both the nature and rates of transformation of natural amphiboles which has proved invaluable in our understanding of the mineralogically-controlled mechanisms of argon release during 40Ar/39Ar dating of amphibole samples.

The system Pd-Fe-Ni-S was studied at 900 and 725°C by means of dry condensed charges. At both temperatures it is dominated by the phase relationships involving sulphide melt. Pd-Fe-Ni alloys with broad miscibility primarily coexist with the melt; they are relatively enriched in Pd, whereas the associated melt is enriched in Ni. With decreasing temperature the melt recedes from Fe-rich regions. The incompatibility of PdS (extensive solid solution with Ni) and mss at 900°C is replaced by their co-crystallization (± disulphide(s) of Ni,Fe or ± sulphide melt) at 725°C The Ni/Fe ratio in the melt changes regularly against that in mss with increasing S fugacity and Pd contents in these two phases. (Ni,Fe)3±xS2 and Pd4S play important roles at 725°C. The data offer an array of distribution coefficients and solubility values suitable for geological interpretations.

Enclaves of diverse origin are present in minor amounts in the coarse-grained biotite granites of the Cornubian batholith, southwest England. The most common enclave type is layered, rich in biotite, cordierite and aluminosilicates, and has textures and compositions that reveal variable degrees of melt extraction from metasedimentary source rocks. Rare sillimanite-bearing enclaves represent residual material, either from the region of magma generation or its ascent path, but most such enclaves were probably derived from the contact aureole closer to the present level of exposure. These non-igneous enclaves (NIE) and their disaggregation products are present in all major plutons, comprising from < 2 to 5 vol.% of the granites. Enclaves of igneous origin are also present in all major plutons except Carnmenellis, generally comprising < 1 vol.% of the granites. The most common type is intermediate in composition, with microgranular texture, and mineral compositions and textures consistent with an origin by magma mixing. Large crystals of K-feldspar, plagioclase and quartz, common in these microgranular enclaves (ME) but absent in NIE, represent phenocrysts derived from the silicic end-member during magma mixing events rather than products of metasomatism as suggested previously. Although the composition of the mafic end-member (basaltic or lamprophyric) involved in the mixing process is poorly constrained, the presence of ME in the granites, and the preponderance of mantle-derived mafic rocks in the coeval Exeter Volcanics, indicate that mafic magma injection into the crust was a factor in the generation of the batholith. Advection of sub-crustal heat provides an explanation for large-volume crustal melting in regions of relatively thin crust such as southwest England.

New chemical analyses, electron and X-ray powder diffraction data, and comparison with gyrolite and reyerite show that tungusite has the ideal formula , symmetry P and a = 9.714(9), b = 9.721(9), c = 22.09(3), α = 90.13(1)°, β = 98.3(2)°, γ = 120.0(1)°, Z = 1. A structural model for tungusite is derived by splitting the double tetrahedral layer of reyerite and inserting a trioctahedral X sheet which is ideally occupied by Fe2+. Polytypism phenomena due to different relative positions between tetrahedral and X sheets are discussed. A substitutional solid solution represented by the formula [Ca14(OH)8]Si24−yAlyO60[NaxM9−(x+z)□z(OH)14−(x+y+2z)·(x+y+2z)H2O] includes tungusite (x = y = z = 0, M = Fe2+ and gyrolite (x = 1, y = 1, z = 6, M = Ca).

The chlorite data presented are from four igneous complexes covering the compositional spectrum of igneous rocks (gabbro to granite) of orogenic and anorogenic settings. The four igneous complexes are; early orogenic gabbro-diorite-tonalite (D-T) suite, late orogenic granodiorite-adamellite (G-A) suite (both are calc-alkaline suites), high-alumina trondhjemite (TR), and anorogenic peralkaline granite (PGR).

Chlorites in these igneous rocks show characteristic compositional fields. The Mg vs Fe plot provides the best discriminant, as data points define three compositionally different groups. Phases in the PGR are Fe-rich, siliceous, interlayered chlorite-smectite (Fe/Mg = 8.6), and differ significantly from those in the calc-alkaline D-T and G-A rocks which are Mg-rich chlorites (Fe/Mg = 0.6–0.8). The X-ray diffraction data for the peralkaline granite samples show superlattice reflections at approximately 31 Å (air-dried) and 34 Å (ethylene glycollated), thus suggesting the presence of an expandable (smectite-like) component in this interlayered (chlorite-smectite) phyllosilicate phase. Chlorites in the peraluminous TR rocks contain Fe/Mg values intermediate between the other two types (Fe/Mg = 1.3). Tetrahedral Al (AlZ) values are remarkably low (0–0.5) in phyllosilicates in the PGR, but vary from 1.9–2.5 in chlorites from the other suites. Yet, these chlorite groups with their generally low AlZ values are distinct from the more stable (type IIb) metamorphic chlorites. Sedimentary chlorites are somewhat similar, in their low AlZ values and metastable structural type, to chlorites in igneous rocks.

In the calc-alkaline rocks, chlorite may have been formed at the expense of both biotite [biotite + 3M + 3H2O = chlorite + A], and calcic amphibole [2 Ca-amphibole + 6H2O + 5O2 + 1.8Al = 1 chlorite + 8SiO2 + A], where M = Fe, Mg, Al, and A = K, Na, Ca. The alteration of alkali amphibole in the peralkaline rocks may have produced interlayered chlorite-smectite via this reaction; [1 Na-amphibole + 7H2O + 2.5O2 + M = 1 chlorite-smectite + A]. The presence of such interlayered chlorite-smectite which typically form at low T (150–200°C) suggests that the region was not affected by any major reheating events, which is consistent with the nature of the feldspars.

The crystal structure, including hydrogen positions, of borcarite, Ca4Mg[B4O6(OH)6](CO3)2, monoclinic, a = 17.840(4), b = 8.380(2), c = 4.445(1) Å, β = 102.04(3)°, V = 649.9(3) Å3, space group C2/m, has been refined by full-matrix least-squares methods to R = 2.5% and wR = 3.0% for 1020 unique observed [|F| ≥ 5σ(F)] reflections collected using Mo-Kα X-radiation. The H positions were located on difference-Fourier maps and were refined using the ‘soft’ constraint that O-H distances are ∼ 0.96 Å. The 4:4T FBB (fundamental building block) of the borcarite structure contains four Bϕ4 tetrahedra (ϕ = unspecified ligand) which share corners to form a four-membered polyhedral ring. Borcarite is the only mineral known to contain this FBB. The FBBs do not polymerize, but each shares three anions with an Mgϕ6 octahedron on either side, forming rods of composition [MgB4O6(OH)6]4- along the c-axis. The rigidity of these rods is enhanced by hydrogen bonding, and individual rods are connected through Caϕ8 polyhedra, Cϕ3 triangles and hydrogen bonds.

Hausmannite (Mn3O4), a manganese oxide with a tetragonally distorted spinel structure, is considered to be ferrimagnetic with a very low Curie temperature of 42.5 K. However, strongly magnetic hausmannite has been discovered in some of the hydrothermally altered high-grade manganese ores of the giant Kalahari manganese deposit in South Africa. EDS-electron microprobe analyses indicate magnetic hausmannite to contain on average between 3 and 11.3 wt.% Fe2O3. In contrast non-magnetic hausmannite contains on average about 1–3 wt.% Fe2O3. X-ray powder diffraction analyses reveal small changes in cell dimensions of the magnetic hausmannite related to the high iron content. Mössbauer spectroscopy suggests that all iron is in the trivalent state. Optical microscopy and scanning electron microscopy (electron back-scatter imaging) proved the magnetic hausmannite to be homogeneous in composition, containing only a few minute inclusions of hematite. Magnetic blocking temperatures of the iron-rich hausmannite, approximating the Curie temperature, are of the order of 750 K. It is suggested that the ferrimagnetic state of hausmannite is stabilized and enhanced by replacement of Mn3+ by Fe3+.

Kusachiite, CuBi2O4, has been found in a calcite vein cutting gehlenite-spurrite skarns at Fuka, Okayama Prefecture. It is associated with calcite, henmilite, sillenite, bakerite, tenolite, bultfonteinite, apophyllite, cuspidine and thaumasite. Kusachiite occurs as prismatic crystals or globular aggregates of platy crystals. It is black, opaque with a metallic lustre. Kusachiite is tetragonal with space group P4/ncc, a = 8.511(2), c = 5.823(2) Å, Z = 4. The strongest lines in the X-ray powder pattern [d in Å (I)(hkl)] are 3.191 (100)(211), 2.695 (18)(310), 1.947 (18)(411), 4.26 (17)(200), 2.913 (16)(002), 2.404 (13)(202), 1.728 (12)(213), and 1.652 (9)(332). The Mohs hardness is 4.5, and the density is 8.5(3) g/cm3 (meas.) and 8.64 g/cm3 (calc.). Cleavage is perfect on {110}. Six electron probe analyses gave the following mean values CuO 13.91, Bi2O3 86.00 and total 99.91 in wt.%. The empirical formula calculated on the basis of O = 4 is Cu0.960Bi2.027O4 with the simplified formula CuBi2O4.

Shannonite, ideally Pb2OCO3, is a new mineral species that occurs as mm-sized white porcellanous crusts, associated with fluorite, at the Grand Reef mine, Graham County, Arizona, USA. Other associated minerals are plumbojarosite, hematite, Mn-oxides, muscovite-2M1, quartz, litharge, massicot, hydrocerussite, minium, and unnamed PbCO3·2PbO. Shannonite is orthorhombic, space group P21221 or P212121, with unit-cell parameters (refined from X-ray powder data): a 9.294(3), b 9.000(3), c 5.133(2) Å, V 429.3(3) Å3, a:b:c 1.0327:1:0.5703, Z = 4. The strongest five lines in the X-ray powder pattern [d in Å (I)(hkl)] are: 4.02(40)(111); 3.215(100)(211); 3.181(90)(121); 2.858(40)(130); 2.564(35)(002). The average of eight electron microprobe analyses is PbO 89.9(5), CO2 (by CHN elemental analyser) 9.70, total 99.60 wt.%. With O = 4, the empirical formula is Pb1.91C1.05O4.00. The calculated density for the empirical formula is 7.31 and for the idealized formula is 7.59 g/cm3. In reflected light, shannonite is colourless-grey to white, with ubiquitous white internal reflections (× 16 objectives), weak anisotropy, barely detectable bireflectance, and no evidence of pleochroism. The calculated refractive index (at 590 nm) is 2.09. Measured reflectance values in air and in oil (× 4 objectives) are tabulated. Transmission electron-microscopy studies reveal that individual crystallites range in size from 10–400 nm, are platy, and are anhedral. Physical properties for cryptocrystalline crusts include: white streak; waxy lustre; opaque; nonfluorescent under both long- and short-wave ultraviolet light; uneven fracture; brittle; VHN100 97 (range 93–100); calculated Mohs’ hardness 3–3½. Shannonite is soluble in concentrated HCl and in dilute HNO3 and H2SO4. The mineral name is for David M. Shannon, who helped collect the samples and who initiated this study.

Kintoreite is a new lead iron phosphate mineral in the alunite-jarosite family, from Broken Hill, New South Wales, Australia. It is the phosphate analogue of segnitite and the iron analogue of plumbogummite. Kintoreite occurs as clusters and coatings of cream to yellowish green rhombohedral crystals up to 2 mm high and with the principal form {112}. The mineral also forms waxy, yellowish green globular crusts and hemispheres on other phosphate minerals. These associated species include pyromorphite, libethenite, rockbridgeite/dufrenite, apatite and goethite. Kintoreite formed during oxidation of primary ore rich in galena, in the presence of solutions with high P/(As + S) ratios. The mineral is named for the locality, the Kintore opencut, in which it is most common. A mineral closely resembling kintoreite in composition has also been found at several mines in Germany. Type material is preserved in the Museum of Victoria and the South Australian Museum.

Electron microprobe analysis showed a nearly complete spread of compositions across the P-dominant portion of the segnitite-kintoreite series. The selected type specimen has an empirical formula of Pb0.97(Fe2.95Zn0.13Cu0.02)Σ3.10[(PO4)1.30(AsO4)0.39(SO4)0.18(CO3)0.11]Σ1.98(OH)5.45·0.74H2O, calculated on the basis of 14 oxygens and with all Fe trivalent. The simplified formula is PbFe3(PO4)2(OH,H2O)6. Kintoreite crystals are translucent with a vitreous to adamantine lustre, with globules appearing waxy. The streak is pale yellowish green and the Mohs hardness is ∼ 4. Crystals show good cleavage on {001} and are brittle with a rough fracture. The calculated density is 4.34 g cm−3. Kintoreite crystals are uniaxial negative with RIs between 1.935 and 1.955 and show light yellowish green to medium yellow pleochroism.

The strongest lines in the X-ray powder pattern are (dobs, Iobs, hkl) 3.07(100) 113; 5.96(90)101; 3.67(60)110; 2.538(50)024; 2.257(50)107; 1.979(50)303; 1.831(40)220. The X-ray data were indexed on a hexagonal unit cell by analogy with beudantite, giving a = 7.325(1) Å, c = 16.900(3) Å, V = 785.3(5) Å3 and Z = 3. The probable space group is Rm, by analogy with beudantite and other members of the alunite-jarosite family. Powder X-ray diffraction data for several intermediate members suggest that the segnitite-kintoreite series may not represent ideal solid solution.

During the study of kintoreite, part of the type specimen of lusungite from Zaïre was obtained and shown to be goyazite. The IMA's Commission on New Minerals and Mineral Names has voted to discredit lusungite as a species, and has approved the renaming of the ‘lusungite’ group as the segnitite group. However, as relationships between crystal structure, order-disorder and solid solution in the Pb-rich minerals of the alunite-jarosite family are not well documented, the nomenclatural changes resulting from this study should be seen as interim only.

Titanites rich in antimony (up to 12.59 wt.% Sb2O5; equal to 0.165 Sb5+ per Si4+ = 1.000) arc described for the first time. They coexist with various greenschist-facies minerals in three different petrographical environments in the manganese concentrations at St. Marcel-Praborna in the Aosta Valley, Italy. These titanites are chemically zoned, the Sb-richest parts generally occurring alongside grain boundaries, microfractures, pores or inclusions. Moderately-good positive correlations exist between the Sb, Al and Fe contents, with negative correlations of each of these elements with Ti. Cr has perturbed the Al and Fe contents since a better negative correlation with Ti is obtained with [Al + Cr + Mn + Fe]. The Sr, Ba, Mn and F contents are rather small and vary irregularly. Several crystal-chemical hypotheses are presented concerning the method of structural formula calculation and the valencies and site distributions of Sb and the companion additional minor elements. The favoured interpretation is to place: Sr2+, Ba2+, Mn2+, Fe2+ and possibly also Sb3+ in the viiCa2+ site; Sb5+, Cr3+, Al3+, Sb3+, Fe3+ and possibly also Mn3+ in the viTi4+ site; and Al3+ in the ivSi4+ site; this indicates the existence of a natural silicate containing not only both trivalent and pentavalent Sb, but also both valencies in the same site. The principal ionic substitution is believed to be: 2 viTi4+ = vi[Al3+ + Cr3+ + Mn3+ + Fe3+] + viSb5+ accompanied by a substantial minor proportion of: 2 viTi4+ = viSb3+ + viSb5, or possibly = 2 viSb4+ The data indicate a very late stage penetration of pre-existing titanites by mobilized Sb, Al, Cr, Mn, Fe, F and presumably also (OH) at this locality, whereas Sr and Ba were mobile at an earlier stage. Manganese, which existed in the sedimentary protoliths, did not enter the titanite structure in very significant quantities.

Cordierite is a characteristic mineral of many peraluminous felsic igneous rocks. A combination of T-P-X parameters, which overlap the stability conditions for felsic magmas, control its formation. Critical among these parameters are relatively low T, low P, and typically high (Mg+Fe2+), Mg/Fe2+, A/CNK, aAl2O3, and fO2. Spatial and textural information indicate that cordierite may originate in one of three principal ways in felsic igneous rocks: Type 1 Metamorphic: (a) xenocrystic (generally anhedral, many inclusions, spatial proximity to country rocks and pelitic xenoliths); (b) restitic (generally anhedral, high-grade metamorphic inclusions); Type 2 Magmatic: (a,b) peritectic (subhedral to euhedral, associated with leucosomes in migmatites or as reaction rims on garnet); (c) cotectic (euhedral, grain size compatibility with host rock, few inclusions); (d) pegmatitic (large subhedral to euhedral grains, associated with aplite-pegmatite contacts or pegmatitic portion alone); and Type 3 Metasomatic (spatially related to structural discontinuities in host, replacement of feldspar and/or biotite, intergrowths with quartz). Of these, Type 2a (peritectic) and Type 2c (cotectic) predominate in granitic and rhyolitic rocks derived from fluid-undersaturated peraluminous magmas, and Type 2d (pegmatitic) may be the most common type in fluid-saturated systems.

Crystal structure refinements were performed on five Al-rich phlogopite-1M crystals (1.50 ⩽ Al3+ ⩽ 1.97 atoms per formula unit) from skarns of the Predazzo and Monzoni Hills petrographic area (north-east Italy) with the aim of characterizing geometrical variation produced by Al3+ increase. The charge imbalance was mostly compensated for by substitutions of highly charged cations in the octahedral sheet (Al3+ and/or Fe3+ for Mg2+). The refinements were carried out in the mean space group C2/m and gave agreement values (R) between 0.025 and 0.030. For some additional crystals, only chemistry and/or unit cell parameters were determined. In all samples the tetrahedra are more regular and larger than those previously reported in the literature for phlogopite crystals and the misfit between tetrahedral and octahedral sheets, produced by the increase in the tetrahedral edges, is mostly compensated for by the tetrahedral ring angle rotation α (10.2 °⩽ α ⩽ 12.5°), whereas the octahedral sheet features seem affected only by local crystal-chemical variations.

Takedaite, Ca3B2O6, has been found in crystalline limestone near gehlenite−spurrite skarns at Fuka, Okayama Prefecture. It occurs as aggregates of granular crystals up to 0.8 mm long and 0.3 mm wide. The mineral is associated with nifontovite, olshanskyite, pentahydroborite, frolovite, sibirskite, calcite and an unidentified mineral, is white or pale gray, and has a vitreous luster. Takedaite is trigonal with space group of Rc, a = 8.638(1), c = 11.850(2)Å, Z = 6. The strongest lines in the X-ray powder pattern [d in A(I)(hkl)] are 2.915(100)(113), 1.895(75)(223), 2.756(61)(104), 2.493(44)(300), 2.044(21) (214,131), 2.160(19)(220), 1.976(18)(006), 1.549(12)(306). The Vickers microhardness is 478 kg mm−2 and the Mohs hardness 4.5. The density is 3.10(2) g cm−3 (meas.) and 3.11 g cm−3 (calc.). Wet chemical analyses give the values CaO 71.13%, B2O3 28.41%, ig. loss 0.14%, and total 99.68%. The empirical formula calculated on the basis of O = 6 is Ca3.053B1.965O6, with the simplified formula of Ca3B2O6.

Monazite is a light rare-earth element (LREE)-bearing accessory phase common in felsic granitic rocks, and strongly influences LREE concentrations in granites and the chemistry of melts and residues formed during partial melting. Cheralite-rich (high-Th) monazite-(Ce) has been recorded as rims on partially dissolved cores in a suite of granulite-facies migmatites generated by disequilibrium melting. High-Th monazite has previously been recorded only in granitic-pegmatite occurrences. Subidiomorphic monazite-(Ce) from leucosome, melanosome and mesosome consists of complexly zoned cores (up to 300 µm in diameter) containing 5.17–9.87 wt.% ThO2, overgrown by essentially unzoned rims (containing up to 21.4 wt.% ThO2). Uranium contents are average for Th-rich monazite-(Ce) (0.22–3.17 wt.% UO2). Th enrichment (relative to LREE) in monazite-(Ce) rims is ascribed to the presence of fluorine-bearing melts (formed during the incongruent breakdown of biotite to produce a water-undersaturated melt), allowing the formation of REE-fluoride complexes in the melt, coupled with the increased charge balanced substitutions Th4+ + Si4+ ⇌ REE3+ + P5+ and Th4+ + Ca2+ ⇌ 2REE3+ into monazite-(Ce). Fractionation of Th and U (reflected by an increased in Th/U in rims relative to cores) may have occurred due to the removal by a CO2-rich fluid phase in the melt. These interpretations are consistent with elevated CO2 and F contents of granitic liquids produced during the water-undersaturated breakdown of biotite under granulite-facies conditions. Evidence for restricted monazite-(Ce)-melt equilibration and rapid melt removal is provided by the ubiquitous presence of partially embayed cores and unzoned rims.