The [4]Al/Si and [6]Al/Mg order-disorder behaviour of minerals in the tremolite-tschermakite solid solution (namely, end-member tschermakite and the 50:50 composition, magnesiohornblende) has been investigated by Monte Carlo simulation, using a model Hamiltonian in which atomic interaction parameters Ji were derived from empirical lattice energy calculations, and chemical potential terms μj (to express the preferences of cations for particular crystallographic sites) were derived from ab initio methods. The simulations performed were increasingly complex. Firstly, ordering in one tetrahedral double chain with Al:Si = 1:3 (tschermakite) was simulated. Although the low-temperature cation distribution in this system was ordered, there was no phase transition (due to the quasi-one-dimensional nature of the system). Next, interactions between tetrahedral Al:Si = 1:3 double chains were included, and a phase transition was observed, with the cation distribution in one double chain lining up with respect to that in the next. Finally, interactions between tetrahedral and octahedral sites were incorporated, to model the whole unit cell, and compositions corresponding to tschermakite and magnesiohornblende were investigated. The whole-cell simulation results compare favourably with experimental conclusions for magnesiohornblende, in that Al at T1 is preferred over Al at T2, and Al at M2 is favoured over that at M1 and M3, but the significant amount of Al at M1 is at odds with experimental observation.

Basalts associated with sapphire deposits are widespread in Europe, Africa, Asia and Australia. In Vietnam, blue, green and yellow sapphires are recovered from eluvial and alluvial placers hosted in basaltic fields of the Dak Lak Province. Two distinct basalt suites are recognized in this field: a tholeiitic suite without any xenocrysts and an alkaline suite with mantle and lower crustal xenocrysts. The sapphires are enriched in Fe (0.43 to 1.26 wt.%), with moderate contents of Cr (33–1582 ppm), Ti (35–1080 ppm), Ga (149–308 ppm) and V (28–438 ppm) and they are poor in Zn and Mg. Their O-isotope compositions range from 6.0 to 6.9% and are not in equilibrium with the alkali basalts which have δ18O values between 5.0 and 5.7%. The U-Pb dating of zircons recovered from the basaltic placers provides evidence of two eruptional events: one at ~6.5 Ma followed by another one at ~1 Ma. The petrography of the basalts and the oxygen isotopic composition of the sapphires suggest that the sapphires are xenocrysts and that they crystallized in a deep magma chamber, at the lower continental lithosphere and the upper mantle boundary, in evolved melts issued from the fractionation of alkali basaltic magmas contaminated with lower crustal fluids.

Coexisting Ba-rich (Cn56–59Or40–42Ab2An0–1) and Ba-poor (Cn7–15Or83–92Ab1–3An0–1) feldspars were found in a jadeitite collected from the Itoigawa-Ohmi district in the Renge high-P/T-type metamorphic belt, Japan. There is an apparent compositional gap in these barian feldspars at Cn15–56 in the ternary system BaAl2Si2O8–KAlSi3O8–NaAlSi3O8. Barian feldspars occur as interstitial phases between subhedral to euhedral jadeite and prehnite, and sometimes cut a jadeite crystal. The occurrence of barian feldspars combined with the texture and mineral assemblages of the host jadeitite suggest that barian feldspars were formed from residual fluids after the formation of jadeite and prehnite from primary aqueous fluids at low-T conditions (<350°C) and pressure of ~0.6 GPa. The Ba content in the residual fluids would increase locally during the formation of jadeite because Ba is incompatible with clinopyroxene. This study supports the suggestion that Ba-rich minerals are not uncommon in jadeitites and albitites/metasomatized rocks that occur as tectonic blocks in serpentinite-matrix mélanges. Barium is an important minor element in metasomatizing fluids related to the formation of jadeitites and might have been derived from subducted oceanic crust at the beginning of the subduction.

The late Cretaceous Kızıldağ ophiolite forms one of the best exposures of oceanic lithospheric remnants of southern Neotethys to the north of the Arabian promontory in Turkey. The ultramafic to mafic cumulate rocks, displaying variable thickness (ranging from 165 to 700 m), are ductiley deformed, possibly in response to syn-magmatic extension during sea-floor spreading and characterized by wehrlite, olivine gabbro, olivine gabbronorite and gabbro. The gabbroic cumulates have an intrusive contact with the wehrlitic cumulates in some places. The crystallization order of the cumulus and intercumulus phases is olivine (Fo86–77)± chromian spinel, clinopyroxene (Mg#92–76), plagio-clase(An95–83), orthopyroxene(Mg#87–79). The olivine, clinopyroxene, orthopyroxene and plagioclase in ultramafic and mafic cumulate rocks seem to have similar compositional range. This suggests that these rocks cannot represent a simple crystal line of descent. Instead the overlapping ranges in mineral compositions in different rock types suggest multiple magma generation during crustal accretion for the Kızıldağ ophiolite. The presence of high Mg# of olivine, clinopyroxene, orthopyroxene, and the absence of Ca-rich plagioclase as an early fractionating phase co-precipitating with forsteritic olivine, suggest that the Kızıldağ plutonic suite is not likely to have originated in a mid-ocean ridge environment. Instead the whole-rock and mineral chemistry of the cumulates indicates their derivation from an island arc tholeiitic (IAT) magma. All the evidence indicates that the Kızıldağ ophiolite formed along a slow-spreading centre in a fore-arc region of a suprasubduction zone tectonic setting.

The crystal structure of whewellite [Ca(C2O4)·H2O] and the dehydration mechanism of caoxite [Ca(C2O4)·3H2O] have been studied by means of differential thermal analysis, X-ray diffraction (powder and single-crystal) analysis and infrared analysis. The first and second analyses confirmed the direct transformation of caoxite into whewellite without an intermediate weddellite [Ca(C2O4)·2H2O] stage. Infrared spectra obtained from caoxite, weddellite and whewellite emphasize the similarity of the O–H-stretching band and O–C–O-stretching band in whewellite and caoxite and the unique bands of weddellite. The structure refinement at low temperature (123 K) reveals that all the hydrogen atoms of whewellite form hydrogen bonds and the two water molecules prop up the crystal structure by the hydrogen bonds that cause a strong anisotropy of the displacement parameter.

Comparing the structural features of whewellite with those of weddellite and caoxite suggests that caoxite and whewellite have a sheet structure consisting of Ca2+ ions and oxalate ions although weddellite does not. It is additionally confirmed that the sheets of caoxite are corrugated by hydrogen bonds but whewellite has flat sheets. The corrugated sheets of caoxite would be flattened by dehydration so the direct transformation of caoxite into whewellite would not occur via weddellite. Essential for this transformation is the dehydration of interlayered water molecules in caoxite leading to the building of the crystal structure of whewellite on its intralayered water molecules. The difference in conformation of water molecules between those two crystal structures may explain the more common occurrence of whewellite than of caoxite in nature.

Naldrettite, Pd2Sb, is a new intermetallic mineral discovered in the Mesamax Northwest deposit, Cape Smith fold belt, Ungava region, northern Québec. It is associated with monoclinic pyrrhotite, pentlandite, chalcopyrite, galena, sphalerite, cobaltite, clinochlore, magnetite, sudburyite (PdSb), electrum and altaite. Other rarer associated minerals include a second new mineral (ungavaite, Pd4Sb3), sperrylite (PtAs2), michenerite (PdBiTe), petzite (Ag3AuTe4) and hessite (Ag2Te). Naldrettite occurs as anhedral grains, which are commonly attached or moulded to sulphide minerals, and also associated with clinochlore. Grains of naldrettite vary in size (equivalent circle diameter) from ~10 to 239 μm, with an average of 74.4 mm (n = 632). Cleavage was not observed and fracture is irregular. The mineral has a mean micro-indentation hardness of 393 kg/mm2. It is distinctly anisotropic, non-pleochroic, has weak bireflectance, and does not exhibit discernible internal reflections. Some grains display evidence of strain-induced polysynthetic twinning. Naldrettite appears bright creamy white in association with pentlandite, pyrrhotite, clinochlore and chalcopyrite. Reflectance values in air (and in oil) for R1 and R2 are: 49.0, 50.9 (35.9, 37.6) at 470 nm, 53.2, 55.1 (40.3, 42.1) at 546 nm, 55.4, 57.5 (42.5, 44.3) at 589 nm and 58.5, 60.1 (45.4, 47.2) at 650 nm. The average of 69 electron-microprobe analyses on 19 particles gives: Pd 63.49, Fe 0.11, Sb 35.75, As 0.31, and S 0.02, total 99.68 wt.%, corresponding to (Pd1.995Fe0.007)2.002(Sb0.982AS0.014S0.002)0.998. The mineral is orthorhombic, space group Cmc21, a 3.3906(1), b 17.5551(5), c 6.957(2) Å , V 414.097(3) Å3, Z = 8. Dcalc is 10.694(1) g/cm3. The six strongest lines in the X-ray powder-diffraction pattern [d in Å (I)(hkl)] are: 2.2454(100)(132), 2.0567(52)(043), 2.0009(40)(152), 1.2842(42)(115), 1.2122(50)(204) and 0.8584(56)(1.17.4).