The Assynt Culmination of the Moine Thrust Belt, in the northwest Scottish Highlands, contains a variety of Caledonian alkaline and calc-alkaline intrusions that are mostly of Silurian age. These include a significant but little-studied suite of dykes and sills, the Northwest Highlands Minor Intrusion Suite. We describe the structural relationships of these minor intrusions and suggest a classification into seven swarms. The majority of the minor intrusions can be shown to pre-date movement in the Moine Thrust Belt, but some appear to have been intruded during the period of thrusting. A complex history of magmatism is thus recorded within this part of the Moine Thrust Belt. New geochemical data provide evidence of a subduction-related component in the mantle source of the minor intrusions.

Feldspars from the Karkonosze pluton (SW Poland) display many features compatible with magma mixing. The mixing hypothesis has been tested using a geochemical mass balance law resulting in two possible paths of magma hybridization. Based on the results of the geochemical calculation, feldspar samples have been chosen along both mixing lines for cathodoluminescence (CL) investigation which was used as the main tool for the reconstruction of their crystallization path. Changes in the conditions of nucleation and crystallization of the feldspars as well as their movement within the magma chamber have been recognized due to different luminescence characteristics. These changes in the conditions of crystallization obtained by CL allow a precise determination of the genetic affinity of the samples to more mafic or more felsic environments.

The results of the present study proved CL to be a valuable tool for the study of crystal-growth morphologies in a dynamic, turbulent environment and also as a geochemical tool for the reconstruction of various petrogenetic mechanisms (e.g. magma hybridization). Accordingly, the combination of CL with geochemical modelling provides corresponding information about magma evolution in an open system.

Several small bodies of massive to banded amphibolite occur within plagioclase-quartz-biotite hornblende gneiss at or close to its boundary with a quartz diorite pluton in the Neoproterozoic terrain of southern Israel. Entrapped within the amphibolite are nodules consisting mainly of calcite+talc, and rare banded marble. Remnant laminae and certain geochemical features such as the negative Ce anomaly and depleted δ13C of the nodules sugggest that they initially formed as stromatolites. The local geological setting of the amphibolites together with the presence of the enclosed meta-carbonates favoured an origin as sediments, although some of the geochemical data point to a basaltic precursor and some of the carbonates have a puzzlingly high (>1000 ppm) Ni content. The origin of the amphibolites is thus enigmatic.

The haüynophyre emitted from a parasitic vent of the Vulture stratovolcano is a S- and Cl-rich, leucitemelilite- bearing lava flow containing an unusually large amount of sodalite-group minerals (>23 vol.%). Mineralogical and chemical study of phenocrysts has led to the identification of black haüynes, blue lazurites and of Cl-rich white or black noseans. X-ray diffraction (XRD) study confirms the occurrence of nosean having a low symmetry (P23). Raman spectra and XRD data show that S is fully oxidized to SO4 in black haüynes and in white noseans, while it is partly reduced to form S3– groups in blue lazurites, which also contain H2O molecules. Structural and chemical data strongly question the validity of the Hogarth and Griffin (1976) method widely used to resolve the ratio S6+/S2– in sodalite-group phases from EMPA data. Among euhedral phenocrysts, large lazurites are only faintly zoned. All other phases show variable core-rim chemical zoning and many phenocrysts are partially resorbed and/or colour-zoned. Black haüynes have highly variable S/Cl and slightly lower SiO2/Al2O3 ratios, larger FeTOT contents and more compatible trace elements than lazurites. Thin opaque noseansodalite rims surrounding all crystals are interpreted as a result of rapid crystallization driven by exsolution of a S-scavenging fluid phase. We suggest that the extreme complexity of the mineralogical assemblage reflects variable aSiO2 and aH2O of the silicate melts.

Skaergaardite, PdCu, is a new mineral discovered in the Skaergaard intrusion, Kangerdlugssuaq area, East Greenland. It occurs in a tholeitiic gabbro associated with plagioclase, clinopyroxene, orthopyroxene, ilmenite, titanian magnetite, fayalite and accessory chlorite-group minerals, ferrosaponite, a member of the annite–phlogopite series, hornblende, actinolite, epidote, calcite, ankerite, apatite and baddeleyite. The mineral is found in composite microglobules composed of bornite, chalcocite, digenite, chalcopyrite, with rare cobalt pentlandite, cobaltoan pentlandite, sphalerite, keithconnite, vasilite, zvyagintsevite, (Cu,Pd,Au) and Pt-Fe-Cu-Pd alloys, unnamed PdCu3, (Pd,Cu,Sn), Au3Cu and PdAuCu. Skaergaardite occurs as droplets, equant grains with rounded outlines, subhedral to euhedral crystals and as irregular grains that vary in size from 2 to 75 μm, averaging 22 μm. It is steel grey with a bronze tint, has a black streak, a metallic lustre and is sectile. Neither cleavage nor fracture was observed. The mineral has a micro-indentation hardness of VHN25 = 257. It is isotropic, non-pleochroic and exhibits neither discernible internal reflections nor evidence of twinning. Skaergaardite varies from bright creamy white (associated with bornite and chalcopyrite) to bright white (associated with digenite and chalcocite). Reflectance values in air (and in oil) are: 58.65 (47.4) at 470 nm, 62.6 (51.1) at 546 nm, 64.1 (52.8) at 589 nm and 65.25 (53.95) at 650 nm. The average of 311 electron-microprobe analyses gives: Pd 58.94, Pt 1.12, Au 2.23, Cu 29.84, Fe 3.85, Zn 1.46, Sn 1.08, Te 0.28 and Pb 0.39, total 99.19 wt.%, corresponding to (Pd0.967Au0.020Pt0.010)Σ0.997(Cu0.820Fe0.120 Zn0.039Sn0.016Te0.004Pb0.003)Σ1.002. The mineral is cubic, space group Pm3m, a = 3.0014(2) Å, V = 27.0378 Å3, Z = 1. Dcalc is 10.64 g/cm3. The six strongest lines in the X-ray powder-diffraction pattern [d in Å (I)(hkl)] are: 2.122(100)(110), 1.5000(20)(200), 1.2254(50)(211), 0.9491(20)(310), 0.8666(10)(222), 0.8021(70)(321). The mineral has the CsCl-type structure. It is believed to be isostructural with wairauite (CoFe), synthetic CuZn (β-brass) and is structurally related to hongshiite (PtCu). Skaergaardite developed from a disordered Pd-Cu-rich metal alloy melt that had exsolved from an earlier Cu-(Fe) sulphide melt. Ordering of Pd and Cu (beginning at T ≈ 600°C) results in development of the CsCl structure from a disordered face-centred cubic structure.

Tertiary ultrapotassic volcanic rocks from Serbia occasionally display low levels of K2O and K2O/ Na2O. In these rocks, analcime regularly appears as pseudomorphs after pre-existing leucite microphenocrysts. The process ofleucite transformation in Serbian ultrapotassic rocks is very thorough: fresh leucite survives only in ugandites from the Koritnik lava flows as well as in rare inclusions in Cpx. This paper focuses on the impact of ‘analcimization’ on the mineralogy and geochemistry ofthe Serbian ultrapotassic rocks, using the samples where leucite survived as a monitor for the process.

Analcimization has had a great impact on the geochemistry of the rocks, but affects only a restricted number of chemical parameters. These are the falsification of the original K2O/Na2O ratio, the decoupling oflarge-ion lithophile elements resulting in considerable depletion of Rb and K2O, but not ofBa, and sporadic, but extreme enrichment ofCs in some analcime-bearing samples (up to 900 ppm). Analcimization is also recognized by an increase in whole-rock δ18O values of ∼3% compared to fresh rocks, which correlates with the level of whole-rock hydration. Finally, the 87Sr/86Sr enrichment at nearly constant 143Nd/144Nd demonstrated by some rocks can also be explained by the analcimization ofleucite. For samples with variable 87Sr/86Sr from the same lava flow, 87Sr/86Sr values correlate with modal analcime abundance (ex-leucite), loss on ignition of whole-rock and whole-rock δ18O values. The extreme depletion in K and enrichment in Na, together with modification of other geochemical parameters, may have led to the misinterpretation of the origin and geodynamic affiliations of the Serbian ultrapotassic rocks, had the effects of analcimization not been taken into account.

A system based on variation of the octahedrally coordinated cations is proposed for graphical presentation and subdivision of tri- and dioctahedral K micas, which makes use of elemental differences (in a.p.f.u.): (Mg – Li) [= mgli] and (Fetot + Mn + Ti – VIAl) [= feal]. All common true tri- and dioctahedral K micas are shown in a single polygon outlined by seven main compositional points forming its vertices. Sequentially clockwise, starting from Mg3 (phlogopite), these points are: Mg2.5Al0.5, Al2.167□0.833, Al1.75Li1.25, Li2Al (polylithionite), Fe22+Li, and Fe32+ (annite). Trilithionite (Li1.5Al1.5), Li1.5Fe2+Al0.5, Fe22+ Mg, and Mg2Fe2+ are also located on the perimeter of the polygon. IMA-siderophyllite (Fe2+2Al) and muscovite (Al2□) plot inside.

The classification conforms with the IMA-approved mica nomenclature and differentiates among the following mica species according to their position in a diagram consisting of mgli and feal axes plotted orthogonally; trioctahedral: phlogopite, biotite, siderophyllite, annite, zinnwaldite, lepidolite and tainiolite; dioctahedral: muscovite, phengite and celadonite. Potassium micas with [Si] <2.5 a.p.f.u. including IMA-siderophyllite, KFe22+ AlAl2Si2O10(OH)2, and IMA-eastonite, KMg2AlAl2Si2O10(OH)2 seem not to form in nature.

The proposed subdivision has several advantages. All common true, trioctahedral and dioctahedral K micas, whether Li-bearing or Li-free, are shown within one diagram, which is easy to use and gives every mica composition an unambiguously defined name. Mica analyses with Fe2+, Fe3+, Fe2+ + Fe3+, or Fetot can be considered, which is particularly valuable for microprobe analyses. It facilitates easy reconstruction of evolutionary pathways of mica compositions during crystallization, a feature having key importance in petrologically oriented research. Equally important, the subdivision has great potential for understanding many of the crystal-chemistry features of the K micas. In turn this may allow one to recognize and discriminate the extent to which crystal chemistry or bulk composition controls the occurrence of some seemingly possible or hypothetical K mica.

Wang et al. (2000) presented interesting new data on the occurrence of Hf-rich zircon in peralkaline granitic rocks. It is shown that the knowledge of the Hf distribution in zircon is important for the understanding of Zr/Hf ratios defined by whole-rock analysis. However, the processes leading to the unusual Zr/Hf fractionation are still poorly constrained. Some aspects are discussed further here. Analysis of available data demonstrates that extremely low Zr/Hf ratios found in topaz- and rare-metal bearing granites may be either a primary signature of some evolved granitic melts or, alternatively, they are produced during albitization of the rocks. Topaz- and rare-metal bearing granites may be P-rich and contain zircon moderately enriched in Hf (2—9 wt.% HfO2). Another group is P-poor and the Hf content in accessory zircon is high (up to 35 wt.% HfO2). Both types of intrusions may occur within a single orogen as demonstrated by the example of the Hercynian magmatism in the Erzgebirge/Krušné hory region (Germany/Czech Republic).

During investigations of the system Sc2O3-Al2O3-TiO2-SiO2, a new, unusual microporous compound, Cs3ScSi8O19, was synthesized as colourless plates from a CsF-MoO3 flux. The crystal structure was determined from single-crystal X-ray diffraction data (Mo-Kα radiation, CCD area detector). The compound is orthorhombic, space group Pnma, with a = 11.286(2), b = 7.033(1), c = 26.714(5) Å, and Z = 4 (R1(F) = 2.6% and wR2all(F2) = 7.3%, using 3066 ‘observed’ reflections with Fo > 4σ(Fo)). The crystal structure of Cs3ScSi8O19 represents a new microporous framework structure type (‘MCV-1’), and the compound is exceptional in being the first representative of a mixed octahedral-tetrahedral framework structure, in which the [TO4]:[MO6] ratio is >6:1. The structure is based on isolated, nearly regular ScO6 octahedra [dav(Sc—O) = 2.112 Å] sharing corners with SiO4 tetrahedra to form an open framework with four-, six- and eight-membered rings; the latter are formed by SiO4 tetrahedra only. Two fully occupied Cs positions are located in large framework voids close to the six-membered rings, whereas four partly occupied and disordered Cs positions are close to very large framework voids bordered by the puckered eight-membered rings. The cavities are linked into channels parallel to [100] and [010]. The structure is compared with that of Cs2TiSi6O15 and related microporous scandium-, REE-, titano- and zirconosilicate minerals and compounds. Cs3ScSi8O19 or derivatives may be important in the context of immobilization of radioactive 137Cs waste, cationic conductivity or catalysis.

Amphibole in the Larvik alkaline plutonic complex in the Oslo rift, Norway, has Ti-rich compositions from edenite through pargasite to kaersutite, and has a large H+ deficiency (0.7–1.1 atoms per formula unit: a.p.f.u.) with a large oxy component in the amphibole OH– site (O2– = 2 – (OH + F + Cl) = 0.2–0.9 a.p.f.u.), similar to the mantle-derived kaersutites. Their compositions reveal a characteristically low Fe3+/(Fe3++Fe2+) ratio (<0.23) and a high F concentration (0.3–0.9 a.p.f.u.). Correlation with the Fe3+ ratio caused by Fe2+ + OH– = Fe3+ + O2– + 1/2H2 substitution is negligible, which is supported by H and O isotope compositions. A possible substitution, [6]Al3+ + OH– = [6]Ti4+ + O2– may be operative for Larvik kaersutites when the O2–/Ti is 1.0. A relatively larger O2–/Ti ratio (1.2—2.0) suggests an another kaersutite substitution mechanism, [6]R2+ + 2OH– = [6]Ti4+ + 2O2–, where [6]R2+ = Fe2+ + Mg + Mn. These effects might result in the limited O2–/Ti ratio value from 1.0 to 2.0.

A negative correlation between Ti and F, suggesting F incorporation into kaersutite may diminish the O2–/Ti ratio, not only due to the occupation of this non-oxy species in the O3 site, but also due to F—Ti avoidance. Composition-dependent H and O isotope variations (δD = –106 to –71% and δ18O = 4.6–5.2%) suggest equilibrium in the closed-system magma with differentiation. The mineral chemistry of Larvik oxy-kaersutitic amphibole could reflect the crystallization in a closed-system magma during rifting with passive crustal thinning at the Oslo palaeorift.

Mineral compositions of small peridotite bodies in an Ordovician collision zone of the Vermont Appalachians provide important clues to their tectonic environment of origin. The bodies have been deformed and partially serpentinized under greenschist- to lower amphibolite-facies conditions during the Ordovician and Devonian. Before serpentinization, the peridotite bodies were dunite as shown by their mineral assemblage and by their high MgO, and low Ti and Al whole-rock contents. Despite deformation and metamorphism, remnant olivine and spinel grains occur; their compositions are taken to represent conditions prior to regional metamorphic events. High Mg/(Mg+Fe) in olivine and very high Cr/(Cr+Al) in spinel indicate that the peridotites formed as highly-depleted mantle residues. The compositions are similar to those in harzburgite and dunite from some ophiolites and from fore-arc regions of subduction zones. Accordingly, the southern Vermont peridotites probably formed in a forearc, supra-subduction zone during the Early Palaeozoic. They were subsequently emplaced by obduction of the upper plate of an east-facing subduction complex.