The Minastira granite, a c. 25 Ma subvolcanic plug of fine-grained granitic rock in the Cordillera Oriental of SE Peru, has preserved textures indicative of a history involving mixing of at least two magmas, a volumetrically dominant felsic component and a less voluminous mafic one. The felsic component is represented by variably fractured, altered and embayed crystals of quartz, feldspar, biotite with minor coarsegrained melt- and fluid-inclusion rich apatite, and possible cordierite (now a pseudomorphous Fe-Mg phase), whereas the mafic component is represented by calcic plagioclase. The process of magma mixing is reflected by: (1) ubiquitous sieved-textured plagioclase with complex textural relationships; (2) a large range in plagioclase compositions with reversals and spike patterns in profiles; (3) embayed and internally fractured (thermal shock?) quartz; (4) the rare occurrence of pyroxene coronas on quartz; and (5) textures within biotite suggestive of its incipient breakdown. The lack of mafic enclaves indicates that physico-chemical conditions of the mixing were conducive to homogenization (i.e. chemical diffusion) and a superficially homogeneous rock is now observed. The association of glomeroclasts of crystals originating from both the mafic and felsic end members and a quenched quartz-feldspar matrix indicate that the mixing occurred in an underlying magma chamber.

The weathering of the Mt. Prinzera serpentinites (Parma province, Northern Apennines, Italy) produced dominant smectite and minor Fe-hydroxides. The mobility of the elements during weathering has been estimated using the ratio Ki = MiS/MiR, where Mi indicates the mass of a generic component i before (R) and after (S) the weathering, and using TiO2 as a practically immobile component. For prevalently to tendentially mobile elements, the degree of mobility, which in our case increases as Ki decreases, is in the order Mn ≈ Cr = Fe < V ≈ Zn ≈ Co < Ni < Si < Mg < Ca. The elements Ti, Ga, Al and Zr are prevalently immobile. The mass chemically removed by the circulating waters during weathering may reach very high values (on average 52% of the original mass of serpentinite) and the main contribution to the mass loss is due to Si and Mg. The composition of the perennial and ephemeral springs in the area is in agreement with the degree of the element mobility at least for Cr, Mg and Ca.

Porphyritic natrocarbonatite lavas erupted from the Oldoinyo Lengai volcano (Tanzania) on 17 October 1995 and 15–19 December 1995 differ from previously studied lavas in that they preserve textures indicative of groundmass carbonate-carbonate immiscibility. The immiscible fractions are considered to involve: a Na-K-Ca-CO2-Cl-rich, F-bearing fluid crystallizing gregoryite, sodian sylvite, potassium neighborite as well as a complex Ba-rich carbonate; and a Na-rich, Cl-poor carbonate liquid approximating to a nyerereite-gregoryite cotectic composition. Compositional data are given for potassium neighborite, this mineral being the first recognized occurrence of a fluorine-based perovskite group mineral in a magmatic environment. New compositional data are also given for a previously recognized potassium iron sulphide which indicate that this phase is probably a solid solution between the ternary sulphides, KFe3S4, K2Fe3S4, and KFe2S3. Textural and paragenetic data are interpreted to suggest that these recent lavas are more evolved than previously investigated Oldoinyo Lengai lavas and that natrocarbonatite is a highly evolved rather than a primitive magma.

Trioctahedral micas in the Karlovy Vary pluton range in composition from Fe-biotites in the granites of the Older Intrusive Complex (OIC) through siderophyllite and lithian siderophyllite to zinnwaldite in the granites of the Younger Intrusive Complex (YIC). Li + AlVI + Si would appear to substitute for Fe2+ + AlIV in biotite with a formula similar to that given in Henderson et al. (1989), but Li + Si appears to substitute for Fe2+ + AlIV in the Li-micas. In mica vs. host rock plots, Rb and F show positive linear covariation except for the Li-mica granites, but femic constituents and tFeO/(tFeO + MgO) have separate trends for OIC and YIC granites and micas. Further differences between OIC and YIC granite micas are seen in their Ti and Mg contents and in plots like V vs. SiO2, AlIVvs. Fe/(Fe+Mg) and Li vs. total iron as Fe2+ and in the results of discriminant analysis. These reveal a geochemical hiatus between OIC and YIC granite micas that coincides with a major temporal hiatus.

Biotite compositions in the YIC granites are similar to those in the granites of the Cornubian batholith and reveal a similar magmatic evolution and genesis in which later biotites evolve to lithian siderophyllites with some enrichment in trace alkalis and F. It is suggested that the biotite granites in the YIC were derived from the products of partial fusion of the OIC granites. A less well-marked geochemical hiatus exists between YIC biotites and zinnwaldites. In some plots (e.g. Si vs. Li, Li vs. tFe) apparent continuity between biotite and the Li-micas suggests continuous evolution, but in others (e.g. Rb vs. TiO2, Rb(biotite) vs. Rb(rock)), Li-mica data points stand apart from the biotites suggesting, like the whole rock data, a separate evolution. Comparison with the more abundant data for Li-micas of the Cornubian batholith suggests derivation of the Li-mica granites by partial fusion of the OIC/YIC granite residues.

Lithium may constitute an essential element in micas, yet it cannot be detected by the electron microprobe. Since Li is critical for correctly classifying micas and properly calculating their formulae, several methods have been proposed to overcome this analytical deficiency. We offer empirical relationships between Li2O and SiO2, MgO, F, and Rb in trioctahedral micas, and between Li2O and F as well as Rb in dioctahedral micas. The resultant regression equations enable lithium contents to be sufficiently well estimated from EPM analyses within the range of validity discussed.

Secondly, we introduce an easy to handle, new diagram with the axis variables [Mg-Li] and [Fetot + Mn + Ti-AlVI] for graphical representation and discuss its scientific rationale. Being based on absolute abundances of cations in the octahedral layer, the diagram provides a simple means to classify micas in terms of composition and octahedral site occupancy, and it also allows compositional relationships between Li-bearing and Li-free mica varieties as well as between trioctahedral and dioctahedral micas to be displayed on a single, two-dimensional diagram.

Blueschist-facies rocks with jadeite-K-feldspar-lawsonite paragenesis occur as exotic blocks in Miocene debris flows in the blueschist belt of northwest Turkey. The jadeite-K-feldspar rocks have a very fine grain size and although recrystallized locally retain a relict porphyritic volcanic texture. The former nepheline microphenocrysts, recognized from their characteristic shapes, are pseudomorphed by jadeite and K-feldspar, while the relict magmatic aegirine has rims of jadeite. The matrix of the rock consists of very fine-grained aggregates of jadeite, K-feldspar and lawsonite. In some blocks, jadeite makes up >60% of the mode. Jadeite, K-feldspar and lawsonite in the blocks are essentially pure end-member in composition. P-T estimates for these rocks are 8 ± 2 kbar and 300 ± 50°C. The preserved volcanic texture, relict aegirine and the bulk rock composition indicate that these rocks represent metamorphosed phonolites. The paragenesis in these rocks shows that jadeite-K-feldspar is a stable mineral pair in blueschist-facies P-T conditions.

Omphacite (Jd46.1–52.0Ae0–8.4Aug48.0–51.2) and diopside (Jd4.3–6.3Ae0–0.4Aug93.6–95.6) coexist in a vein cutting an omphacitite block in a serpentinite melange of the Oeyama ophiolite, central Chugoku Mountains. The compositional gap between omphacite and diopside is significantly wider than for other omphacitediopside pairs reported in the literature. The intergrowth texture of the omphacite-diopside vein suggests that the clinopyroxene pair was contemporaneously crystallized in the fracture from a Ca-bearing, alkali-rich fluid in a sub-solvus condition. Such a fluid may have been introduced from the surrounding serpentinized clinopyroxene-bearing harzburgite. The stability of omphacite and Al-rich pumpellyite in the matrix and the omphacite-diopside vein indicate that the earlier matrix recrystallization and later fracture filling may have both taken place under high-P-T condition during the melange-forming stage.

Alkali-deficient tourmalines are found in albitized rocks from the hanging-wall of the Sullivan Pb-Zn-Ag deposit (British Columbia, Canada). They approximate the Mg-equivalent of foitite with an idealized formula □(Mg2Al)Al6Si6O18(BO3)3(OH)4. Major chemical substitutions in the tourmalines are the alkali-defect type [Na*(x) + Mg*(Y) = □(x) + Al(Y)] and the uvite type [Na*(x) + Al(Y) = Ca(x) + Mg*(Y)], where Na* = Na + K, Mg* = Mg + Fe + Mn. The occurrence of these alkali-deficient tourmalines reflects a unique geochemical environment that is either alkali-depleted overall or one in which the alkalis preferentially partitioned into coexisting minerals (e.g. albite).

Some of the alkali-deficient tourmalines have unusually high Mn contents (up to 1.5 wt.% MnO) compared to other Sullivan tourmalines. Manganese has a strong preference for incorporation into coexisting garnet and carbonate at Sullivan, thus many tourmalines in Mn-rich rocks are poor in Mn (<0.2 wt.% MnO). It appears that the dominant controls over the occurrence of Mn-rich tourmalines at Sullivan are the local availability of Mn and the lack of other coexisting minerals that may preferentially incorporate Mn into their structures.

The Las Aguilas Ni-Cu-PGE deposit is associated with a sequence of basic-ultrabasic rocks made up of dunite, harzurgite, norite and amphibolite. These igneous (partially metamorphosed) rocks, and their host granulites, gneisses and migmatites of probable Precambrian age, are highly folded. The sulphide ore, consisting of pyrrhotite, pentlandite and chalcopyrite, occurs in the cores of both antiform and synform structures, within dunite, harzburgite and mainly along shear zones in bronzitite, replacing small mylonitic subgrains. The platinum-group mineral assemblage is dominated by Pd bismuthotellurides (Pt-free merenskyite, palladian bismuthian melonite and michenerite), with minor sperrylite, and PGE-sulpharsenides. The latter often occur as single, zoned crystals frequently showing cores of irarsite; outside these are concentric zones of cobaltian hollingworthite, rhodian nickelian cobaltite and Fe-rich nickelian cobaltite.

Mineralogical, textural and chemical evidence indicate that the sperrylite and platinum-group element sulpharsenides were formed during a primary magmatic event associated with the fractionation of a basaltic melt, which was contaminated by the assimilation of metamorphic crustal rocks. PGE sulpharsenides crystallized from As-bearing, residual magmatic liquids that collected PGE and segregated after the crystallization of the monosulfide solid solution. During high-grade metamorphism, sulpharsenides were remobilized as solid crystals in the liquated sulfides suffering partial dissolution and fracturing. On the other hand, there is no evidence of a primary concentration of Pd-bismuthotelluride minerals, and their present spatial distribution is only the consequence of their formation under high- to medium-grade metamorphism, down to temperatures of below 500°C. Pd bismuthotellurides crystallize even in fractures of sulpharsenides, attached to the boundaries of highly dissolved sulpharsenide crystals, and intergrown with molybdenite.

Gold in Early Proterozoic Birimian greenstone at Prestea in Ghana is associated with base metal sulphides and sulphosalts including arsenopyrite, pyrite, sphalerite, chalcopyrite, pyrrhotite, galena, tetrahedrite, bournonite, boulangerite and jamesonite. The occurrence of the gold is intimately associated with arsenopyrite and the sulphosalts, and to a lesser extent with the other sulphides. The tetrahedrites at Prestea constitute the major component of sulphosalts associated with gold and occurring in two distinct types. Type I show ideal stoichiometric composition. Type II tetrahedrites deviated from the ideal stoichiometry and are represented approximately by the average formula (Cu,Ag)9.61(Fe,Zn)2.39(Sb,As)4S13. The tetrahedrites co-precipitated with gold exhibit ideal characteristics indicating an equilibruim state of the mineralizing fluid during precipitation. Three types of pyrites were distinguished by electron-microprobe analyses based on their As, Co and Ni composition. The As content in type I vary from 0.15 to 0.37 wt%, and contain up to 2 wt.% Co.Type II pyrites are As-rich and form the most dominant with As content ranging from 0.2 to 2.69 wt.%. Ni content varies from below-detection to 1000 ppm. Type III pyrites are poor in the trace elements and consistent with the stoichiometric composition. The mineralization occurred in three paragenetic stages from at least a two-phase hydrothermal fluid, with stage II forming a prolonged and main stage of the ore and gold mineralization. Redox changes in ore fluid which were triggered by episodic pressure releases during fissuring and fracturing caused fluctuation of the activity of the As/Ni ratio and subsequent oscillatory zoning of Ni in As-rich ores.