Polyminerallic, sulphidic mine wastes were treated with KH2PO4-H2O2 solutions to determine whether the formation of solid phosphate coatings inhibits sulphide oxidation and metal and metalloid mobility. The waste rocks were metal (PbZnCu) and metalloid (AsSb) rich and consisted of major quartz, dickite, illite and sulphide minerals (e.g. galena, chalcopyrite, tetrahedrite, sphalerite, pyrite, arsenopyrite) as well as minor to trace amounts of pre- and post-mining oxidation products (e.g. oxides, hydroxides, arsenates and sulphates). Scanning electron microscopy observations of the waste material treated with KH2PO4-H2O2 solutions showed that metal, metal-alkali and alkali phosphate precipitates formed and coatings developed on all sulphides (with the exception of tetrahedrite). The abundance of phosphate phases was dependant on the availability of metal and alkali cations in solution. In turn, the release of cations was dependent on the amount of sulphide oxidation induced during the experiment or the presence of soluble oxidation products. Lead and to a lesser degree Cu and Zn phosphate coatings remained stable during H2O2 leaching, preventing acid generation and metal release. In contrast, the lack of phosphate coating on tetrahedrite and arsenopyrite allowed oxidation and leaching of As and Sb to proceed and mobilized As and Sb did not form phosphate phases. As a result, As and Sb displayed the greatest release from the coated waste. Thus, the application of KH2PO4-H2O2 solutions to partly oxidized, polyminerallic mine wastes suppresses sulphide oxidation and is most effective in inhibiting Pb (Cu and Zn) release. However, the technique appears ineffective in preventing metalloid (As, Sb) leaching from tetrahedrite- and arsenopyrite-bearing wastes.

Forearc peridotite is generally characterized by low Mg# (= Mg/[Mg + Fe2+] atomic ratio) at a given Cr# (= Cr/[Cr + Al] atomic ratio) of chromian spinel compared to common abyssal peridotite. This may be due to (1) smaller modal abundance of spinel and/or (2) lower equilibrium temperature, for the forearc peridotite. Forearc peridotite has the same amount of spinel as abyssal peridotite, eliminating the first possibility. Spinel in harzburgite and dunite from the Hahajima Seamount at the Izu-Bonin forearc, has a large Cr#, >0.57, and the Mg# is slightly variable towards low values at a given Cr#. The Mg# of spinel cores decreases strongly with a decrease in size. This is due to cooling along with hydration, which gave rise to a compositional variation of Ca-amphibole, from edenitic hornblende (high-temperature) to tremolite (low-temperature) in the Hahajima peridotite. The average two- pyroxene temperature of the Hahajima peridotite, 921°C, is less than that of the abyssal peridotite (1138°C), which is not consistent with a size-dependent Mg# of spinel for the latter. Forearc peridotite has been cooled effectively by H2O released from the subducted slab, causing a small Mg# of their spinels.

The Pan-African orogenic shield rocks of eastern Egypt were intruded by several anorogenic within- plate granitic complexes, including Mounts Abu-Kharif and El-Dob. These two massifs were emplaced at the intersection of a fault system and a shear zone. The two massifs are made up of hypersolvus peralkaline granites, consisting essentially of perthitic alkali feldspar (55–65 vol.%), quartz (30–35%), and alkali amphibole (ferrorichterite to arfvedsonite; 5–12%), with accessory zircon, apatite and ilmenite. The rocks are evolved in composition, are relatively enriched in Nb (53–75 ppm), Y (34–72 ppm), Zr (421–693 ppm), Ga (26–29 ppm), and the REE (294–562 ppm), and depleted in Al, Mg, Ca, Sr, Ba and Eu. The REE patterns are sub-parallel, LREE -enriched over HREE , and show prominent negative Eu anomalies. The rocks exhibit mineralogical and chemical traits typical of within-plate A-type granites. Rb-Sr radiometric age dating produced a Cambrian age of 522±21 Ma, and an initial 87Sr/86Sr ratio of 0.7080±0.0042. Thus, the investigated peralkaline granitic rocks were emplaced following the termination of the Pan-African orogeny. The rocks are interpreted to have formed in an extensional tectonic environment during a phase of cooling, relaxation, crustal attenuation, and fracturing of the newly-formed shield.

Results of geochemical modelling indicate that the magma may have formed by a large degree of batch partial melting (F = 0.57) of Pan-African calc-alkaline shield rocks, which had been metasomatized possibly by a Na-rich fluid. The volatile flux may have caused fenitization-type reactions along fissures and re-activated Pan-African fractures prior to anatexis, and is considered to have played a role as an important agent of heat transfer. Shear heating, caused possibly by a rapid change in the direction of plate motions beneath eastern Egypt during the Early Palaeozoic, is likely to have produced temperatures necessary for crustal anatexis. The confining pressure must have been released by fissuring of the crust. Magma ascent may have been facilitated by reactivation of pre-existing Pan-African fractures.

Detrital chrome-spinels are contaminant grains within ilmenite concentrates produced from heavy-mineral deposits along the coast of southeast Africa. The presence of even minor levels of chromia in the predominantly ilmenite-rich concentrates, downgrades their market value as potential feedstocks for the production of titania pigment. An understanding of their composition can assist in their removal from the ilmenite concentrates.

Compositions from a database of close to 900 chrome-spinel analyses shows the major element components and their ranges (in wt.%) are: Cr: 0.4-45.3, Al: 0.0-31.0, Fe: 8.5-69.6 and Mg: 0.0-12.2. Minor components include Ti: 0.1-11.4 and Zn: 0.0-13.7.

The chrome-spinel data fall into two compositionally distinct groups. The first group of spinels is dominated by a strong trend reflecting the mutual substitution between Al3+ and Cr3+ in the spinel structure. The second group of spinels is characterized by compositions containing abundant Fe3O4magnetite component. The clear division between chrome-spinel compositional types indicates the grains are derived from at least two chemically dissimilar provenances.

The compositional differences between the chrome-spinel groups has a positive impact on subsequent ilmenite upgrading treatments as the spinels which contain the highest magnetite component are easily removed via low-intensity magnetic separation procedures.

Single crystals of Sr feldspar (SrAl2Si2O8, space group: I2/c) were treated isothermally in the temperature range between 1410 and 1640°C, in order to determinate the evolution of the Al,Si configurations at equilibrium with thermal treatments. X-ray intensity data collection and structural refinement were performed on the quenched crystals. Significant modifications were observed in the average tetrahedral distances and therefore in Qod values.

Two different series of thermal treatments were performed: (1) a crystal of ordered Sr feldspar (Qod= 0.85) was progressively disordered at 1560°C (Qod = 0.82), at 1610°C (Qod = 0.74) and at 1640°C (Qod = 0.69); (2) another crystal with Qod = 0.72 (obtained by annealing a glass at T =1625°C), was ordered at T = 1600° (Qod = 0.75).

As already observed in anorthite quenched from 1530°C (Qod = 0.78), also in Sr feldspar, annealing near Tmelt, caused significant disorder in the Al-Si configuration (Qod = 0.69).

Observations by transmission electron microscopy show an increase in the average size of the i-type antiphase domains up to 5000Å in the samples quenched from 1640°C, in comparison with samples annealed at 1450°C (∼ 2000 Å). The modifications observed in the Al,Si configurations are due to intradomain disorder.

Yukonite, a rare arsenic-bearing hydrous mineral, the crystal symmetry and variety in chemical composition of which have so far been insufficiently studied, has been found in the modern deposit of Nalychevskie hot springs in Central Kamchatka, Russia. This is the first finding of yukonite in Eastern Eurasia and Siberia. Yukonite specimens from Nalychevskie hot springs and from Venus Mine in Yukon Territory, Canada, have been investigated using an analytical transmission electron microscope (TEM). Yukonite is a crystalline substance with extremely thin (~5 nm) platy morphology. Yukonite from Venus Mine forms brittle aggregates in which grains are irregularly bent and randomly distributed. At Nalychevskie hot springs, yukonite occurs as single plates, coexisting with some amorphous material of similar composition. Intensity distributions in electron diffraction indicate that most plates of yukonite at Nalychevskie hot springs have orthorhombic symmetry, but some are hexagonal with ahex = 11.3 Å. The orthorhombic cell is C-centred with aorth = √3ahex, borth= ahex. High-resolution images of edge-on mounts indicate that the periodicity normal to the planes is d001=11.2 Å. Yukonite from Nalychevskie hot springs contains anomalously high Si relative to that in yukonite from Venus Mine and that reported previously. Strong negative correlation between As and Si indicates that Si substitutes for As in the structure.

Platinum group mineral (PGM) assemblages in the Platreef at Sandsloot, northern Bushveld Complex, in a variety of lithologies reveal a complex multi-stage mineralization history. During crystallization of the Platreef pyroxenites, platinum group elements (PGE) and base-metal sulphides (BMS) were distributed thoughout the interstitial liquid forming a telluride-dominant assemblage devoid of PGE sulphides. Redistribution of PGE into the metamorphic footwall by hydrothermal fluids has formed arsenide-, alloy- and antimonide-dominant assemblages, indicating a significant volatile influence during crystallization. Serpentinization of the footwall has produced an antimonide-dominant PGM assemblage. Parts of the igneous reef were subjected to alteration by a late-stage, Fe-rich fluid, producing ultramafic zones where the telluride-dominant assemblage has been recrystallized to an alloy-dominant one, particularly rich in Pt-Fe and Pd-Pb alloys. A thin, small-volume zone of PGE-BMS mineralization along the base of the hangingwall contains a primary PGM assemblage that is locally altered to one dominated by Pt/Pd germanides. This is thought to have formed when the new pulse of Main Zone magma entered the chamber, and scavenged PGE from the underlying Platreef pyroxenites. That each major rock type at Sandsloot contains a distinctive PGM assemblage reflects the importance of syn- and post-emplacement fluid and magmatic processes on the development of Platreef mineralization.

Natrocarbonatite lavas erupted from hornitos T37B and T49B at Oldoinyo Lengai (Tanzania) during 23–30 July, 2000 are unusual in containing sylvite and fluorite microcrysts together with fluorite-nyerereite intergrowths. The latter are relatively coarse grained and exhibit granular textures indicative of slow crystallization rates relative to those of their host subaerial lavas. Fluorite microcrysts are considered to be derived by the fragmentation of the fluorite-nyerereite clasts. Sylvite microcrysts contain inclusions of ferroan alabandite [(Mn0.67-0.71Fe0.33-0.29)S] and are poor in Na (1.9–7.7 wt.% Na; 6.1–23.4 mol.% NaCl). Intergrowth and microcrystal fluorite contains 1–3.5 wt.% Sr. Intergrowth nyerereite has a composition similar to that occurring as bona fide phenocrysts. The groundmass of lava erupted from hornito T37B contains nyerereite microphenocrysts (4–8 wt.% BaO) that are epitaxially mantled by barian nyerereite (12–20 wt.% BaO). The latter are compositionally and texturally distinct from the groundmass phase X, which is considered to be a burbankite-group mineral. The fluorite-nyerereite clasts are considered to be derived from the magma chamber underlying hornitos T37B and T49B, and thus representative of some of the products of crystallization of natrocarbonatite magma under hypabyssal conditions. The origins of the sylvite microcrysts cannot, as yet, be determined.

A synthetic analogue, Ca(Ti0.6Al0.2Ta0.16Nb0.04)OSiO4, of an aluminoan tantalian titanite previously described from Craveggia pegmatite (Piemonte, Italy) has been prepared by a ceramic synthesis technique and its crystal structure determined by Rietveld analysis of the powder X-ray diffraction pattern. The synthetic Al-Ta-Nb-rich titanite adopts space group A2/a implying that substitutions at the single octahedral site destroy the coherence of the off-centering of octahedral chains in the titanite structure resulting in a P 21/a → A2/a phase transition. Unit-cell dimensions obtained for the Al-Ta-Nb-rich titanite are: a = 7.0649(1) Å; b = 8.7187(1) Å; c = 6.5701(1) Å; β = 113.755(1)°, V = 370.41(1) Å3. The extensive replacement of Ti by Al, Ta and Nb results in a considerable decrease in the distortion of all coordination polyhedra in the structure of this titanite. These structural data suggest that a solid solution CaTi1-x(Alx /2 [Ta,Nb]x /2)OSiO4 (0 ≤ x ≤ 0.4) adopting the titanite structure might exist.

Kalungaite, PdAsSe, is a new mineral discovered in the Buraco do Ouro gold mine, Cavalcante town, Goiás State, Brazil. It occurs in a quartz-muscovite mylonite, related to a peraluminous granite, in platy anhedral aggregates along foliation planes. Associated ore minerals are gold, chalcopyrite, bohdanowiczite, an unnamed Pb-Bi-Se-S mineral, clausthalite, guanajuatite, stibiopalladinite, sperrylite and padmaite. Gangue minerals are muscovite, quartz and rare tourmaline and magnetite. Kalungaite is lead-grey, has a metallic lustre, a black streak and is brittle with uneven fracture. No cleavage was observed. The mineral has a micro-indentation hardness of VHN25 = 438 (range of 429–455 kg/mm2 from five indentations). Under reflected light, kalungaite is cream, or creamy grey adjacent to gold grains, has no internal reflections and is isotropic. Reflectance values in air (and in oil) are: 47.5 (33.3) at 470 nm, 46.9 (32.6) at 546 nm, 46.8 (32.6) at 589 nm and 48.0 (34.0) at 650 nm. The average of eight electron-microprobe analyses gives: Pd 41.32, As 27.49, Bi 0.35, Sb 1.59, Se 27.67 and S 1.22, total 99.64 wt. %, corresponding to Pd1.006(As0.950Sb0.034Bi0.004)Σ0.988(Se0.908S0.099)Σ1.007Kalungaite is cubic, space group Pa, a = 6.089(4) Å, V = 225.78 Å3, Z = 4. Dcalc is 7.59 g/cm3. The strongest seven X-ray powder-diffraction lines [d in Å(I)(hkl )] are: 3.027(75)(002), 1.838(100)(113), 1.172(95)(115, 333), 1.077(80)(044, 144, 334), 0.988(70)(116, 235, 253), 0.929(90)(335) and 0.918(70)(226). Kalungaite is interpreted as having formed from hydrothermal fluids of granitic origin, during syn-emplacement shearing and alteration, producing an unusual gold-platinum-group element deposit.

Paratooite-(La) is a new lanthanum-dominant rare-earth copper carbonate from the Paratoo copper mine, near Yunta, Olary district, South Australia. Paratooite-(La) occurs as sheaves and radiating sprays of blade-like to tabular pale blue crystals in thin fissures in a slaty country rock. Individual crystals are typically 50–200 μm in maximum dimension but <5 μm thick. Associated minerals include donnayite-(Y), kamphaugite-(Y), and bastnäsite-(La). Electron microprobe and CHN analyses gave: La2O3 26.47; Pr2O3 7.74; Nd2O3 8.15; Sm2O3 0.66; Gd2O3 0.85; Y2O3 0.72; CaO 7.57; SrO 3.15; Na2O 3.3; CuO 5.77; F 0.24; CO2 32.05; NO2 1.12; -O=F -0.10; sum 100.03, yielding an empirical formula of (La3.54Ca2.94Na2.32Nd1.05Pr1.03Sr0.66Y0.14Gd0.10Sm0.08)Σ11.86Cu1.58(C15.84N0.53)O47.76F0.24. The simplified formula is (REE ,Ca,Na,Sr)6Cu(CO3)8 or possibly REE3(Ca,Sr)2NaCu(CO3)8. The mineral is pale turquoise-blue to pale blue in colour, transparent, with a pearly to vitreous lustre and a pale blue streak. No cleavage was observed but the morphology and TEM studies indicate a cleavage parallel to ﹛100﹜. The Mohs hardness is estimated to be 4. The strongest lines in the X-ray powder pattern are [dobs (Iobs) (hkl )]: 5.047 (53) (200); 4.786 (49) (021); 3.957 (43) (220); 3.468 (43) (012, 221); 2.927 (100) (202); 2.530 (52) (241); 2.344 (22) (420,103); 2.232 (20) (421). A synchrotron powder diffraction pattern was indexed on a primitive orthorhombic cell with a = 10.0862(5), b = 12.8088(6), c = 7.2360(4) Å, V= 934.8(1) Å3 and Z = 2. The crystal structure of the new mineral could not be determined but powder diffraction data indicate the space group is probably P 222, Pmmm , P 2221 or Pmm2. The measured density is 3.68(3) g/cm3 and the calculated density is 3.78 g/cm3. Paratooite-(La) is biaxial negative with α = 1.605(3), β = 1.696(3) and γ = 1.752(2); pleochroism is medium strong; X very pale bluish, Y and Z bluish (with greenish tint) with absorption Z ≈ Y >> X. Paratooite-(La) is a supergene mineral which precipitated from mildly basic carbonated groundwaters. The mineral is named for the type locality.