Pyrite, the most widespread and abundant of sulphide minerals in the Earth's surficial rocks, commonly constitutes the primary opaque phase in ore deposits. Consequently, an understanding of the behaviour of pyrite and its relationships with coexisting phases during the metamorphism of pyritebearing rocks is vital to the interpretation of their genesis and post-depositional history. Metamorphism is commonly responsible for the obliteration of primary textures but recent studies have shown that the refractory nature of pyrite allows it to preserve some pre-metamorphic textures. Pyrrhotite in pyritic ores has often been attributed to the breakdown of pyrite during metamorphism. It is now clear that pyrrhotite can be primary and that the presence of pyrrhotite with the pyrite provides a buffer that constrains sulphur activity during metamorphism. Pyrite-pyrrhotite ratios change during metamorphism as prograde heating results in sulphur release from pyrite to form pyrrhotite and as retrograde cooling permits re-growth of pyrite as the pyrrhotite releases sulphur. Retrograde growth of pyrite may encapsulate textures developed during earlier stages as well as preserve evidence of retrograde events. Sulphur isotope exchange of pyrite with pyrrhotite tends to homogenise phases during prograde periods but leaves signatures of increasingly heavy sulphur in the pyrite during retrograde periods.

Metamorphosed stratabound iron- and base-metal sulphide deposits often exhibit microtextures in which fractures in cataclastically-deformed pyrite porphyroblasts are filled with matrix sulphides; chalcopyrite, sphalerite, pyrrhotite or galena. Discussions of such textures have mostly centred on whether solid-phase or fluid-phase mechanisms were responsible for the movement of the matrix sulphides.

The small Zn-Cu sulphide body at Gressli, in the central Norwegian Caledonides, shows these textural features to an extreme degree. Both chalcopyrite and sphalerite show heavy replacive relations to the cataclastically deformed metablastic pyrite, along fracture walls and grain boundaries. They also occur injected along the opened-up triple junctions of foam-textured pyrite. In addition, parts of the ore show patchy quartz with clear replacive relationship to all three sulphides, a feature not often reported from such ores. Such textures can be interpreted to support a mobilisation sequence chalcopyrite-sphalerite-quartz within the Gressli ore. Their extent and degree of development indicate that fluid-phase mobilisation of the three minerals must have played a dominant role. Chalcopyrite and sphalerite are most likely derived from within the ore-mass itself; an external source for the SiO2 seems most probable, in the form of metahydrothermal solutions moving along retrograde shear zones at or near ore-walls.

Neutron diffraction texture goniometry indicates that naturally deformed polycrystalline pyrite ores from Mt. Lyell (Tasmania) and Degtiarka (Ural Mountains) have weak lattice preferred orientations. During experimental deformation involving dislocation flow at elevated temperatures and pressures, these initial fabrics have been modified to produce new lattice preferred orientations.

Polycrystalline pyrite form Mt. Lyell (B-1) has an initial <111> - fibre texture perpendicular to a grain-size layering. After 24% shortening perpendicular to the <111> - fibre axis at 700°C a new, but weak <100> texture has developed parallel to the shortening axis. The Degtiarka pyrite (PN-6) initially has two weak fibre components. The somewhat stronger component is a <100>-fibre texture, similar to that in the experimentally deformed B-1 pyrite. The other one is a <111> - fibre texture similar to the intital B-1 preferred orientation. After 30% shortening oblique to both initial fibre axes at 600°C weak <110>- and <111>-fibre textures have developed. The experimentally produced fabrics have developed during deformation involving dislocation flow, dynamic recrystallisation and some microcracking. Intergranular sliding may also have been involved. Differences between lattice preferred orientations developed in the 600°C and 700°C experiments are interpreted to indicate a change in the dominant flow mechanism with changing temperature.

In comparison with other cubic minerals that have been deformed experimentally by dislocation flow mechanisms, the pyrite shows an unusually weak preferred orientation which can be detected only by means of neutron diffraction texture goniometry.

Chalcopyrite samples from Mt Isa, Australia have been experimentally shortened by up to 30% at temperatures up to 450°C at a constant confining pressure of 300 (400) MPa, and different strain rates in the range from 10-5 to 10-8 sec-1. After deformation, the X-ray pole figures show a maximum of (220/204) perpendicular to the compression axis for each of the samples, which has already been described for room temperature experiments by Lang (1968). The overlapping pseudocubic peaks of chalcopyrite can be separated into true tetragonal peaks by neutron diffraction texture analysis using a position sensitive detector combined with profile analysis (Will et al., 1989). The five investigated samples each show a combination of two or four main orientations of the crystallites, which represent neither a pseudocubic nor a tetragonal fibre texture.

The Vangorda Pb-Zn-Ag orebody is a 7.1 M tonne, polydeformed stratiform massive sulphide deposit in the Anvil mining district, Yukon, Canada. Five sulphide lithofacies have been identified within the desposit with a typical mineralogy of pyrite, sphalerite, galena, and barite. Pyrrhotite-sphaleritemagnetite assembalges are locally developed. Etched polished sections of massive pyrite ores display relict primary depositional pyrite textures such as colloform growth zoning and spheroidal/framboidal features. A wide variety of brittle deformation, ductile deformation, and annealing textures have been identified. Brittle deformation textures include thin zones of intense cataclasis, grain indentation and axial cracking, and grain boundary sliding features. Ductile deformation textures include strong preferred grain shape orientations, dislocation textures, grain boundary migration, dynamic recrystallisation and pressure solution textures. Post deformational annealing has produced grain growth with lobate grain boundaries, 120° triple junctions and idioblastic pyrite porphyroblasts. The distribution of deformation textures within the Vangorda orebody suggests strong strain partitioning along fold limbs and fault/shear zones, it is postulated that focussed fluid flow in these zones had significant effects on the deformation of these pyritic ores.

The copper-bearing stratabound pyritic massive sulphide bodies contained in metamorphosed basic eruptives of Ordovician age at Sulitjelma in Nordland County, Norway, form one of the important fields of sulphide mineralisation within the Köli Nappe Complex. The sulphide bodies and their enclosing rocks were subject to successive stages of penetrative deformation and recrystallisation during the cycle of metamorphism and tectonic transport caused by the Scandian Orogeny. Textures within the ores and the immediate envelope of schists show that strain was focused along the mineralised horizons. The marked contrast in competence between the massive pyritic sulphides and their envelopes of alteration composed dominantly of phyllosilicates, and the metasediments of the overlying Furulund Group, led to the formation of macroscale fold and shear structures. On the mesoto microscale, a variety of textures have been formed within the pyrite-pyrrhotite-chalcopyrite-sphalerite sulphide rocks as a result of strain and recrystallisation. Variations in pyrite:pyrrhotite ratios and in the texture and proportions of associated gangue minerals evidently governed the strength and ductility of the sulphide rocks so that the same sulphide mineral can behave differently, displaying different textures in different matrices. In massive pyritic samples there is evidence of evolution towards textural equilibrium by recrystallisation, grain growth and annealment during the prograde part of the metamorphic cycle. Later, brittle deformation was superimposed on these early fabrics and the textural evidence is clearly preserved. By comparing published data on the brittle-ductile transformation boundaries of sulphide minerals with the conditions governing metamorphism at Sulitjelma, it is concluded that most of the brittle deformation in the sulphides took place during or after D3 under retrograde greenschist conditions. Grain growth of pyrite in matrices of more ductile sulphides during the prograde and early retrograde stages of metamorphism produced the coarse metablastic textures for which Sulitjelma is well-known. In some zones of high resolved shear stress, pyrite shows ductile behaviour which could be explained by a dislocation flow mechanism operating at conditions close to the metamorphic peak. In those horizons in which pyrrhotite is the dominant iron sulphide, the contrast in ductility between silicates, pyrite and pyrrhotite has led to the development of spectacular tectonoclastic textures in which fragments of wall rock have been broken, deformed, rolled and rotated within the ductile pyrrhotite matrix.

Sulphide mylonites are fine-grained massive sulphides which have deformed in a plastic manner. In the Renström Zn-Pb-Cu-Ag-Au VMS deposit, one of several operating mines in the Early Proterozoic Skellefte District in Northern Sweden, shear-zone metamorphism has resulted in the development of mylonitic fabrics within the sulphides. The massive sulphide ore is hosted in a shallow submarine to subaerial volcano-sedimentary sequence which has been variably metamorphosed and deformed. Initially, the sequence underwent burial metamorphism which was followed by an amphibolite grade regional metamorphic event at pressures of around 7.5 kbar and temperatures of 540-600°C This has been overprinted by a retrogressive metamorphic event at greenschist facies (at ca. 400°C with concomitant ductile deformation. Finally the area was uplifted to shallower crustal levels with associated cataclastic deformation.

Both the regional and dynamic metamorphic events have resulted in the development of specific textures in the sulphide ores. Textural evidence indicates that pressure solution has been mainly responsible for the plastic deformation in pyrite, while the weaker sulphide minerals such as pyrrhotite, chalcopyrite and galena have generally recrystallised in response to the high strains.

Sulphide mylonites are probably common rocks in many polydeformed massive sulphide deposits like Renström. They may have previously been misinterpreted as primary depositional textures.

A calcite-rich block in nephelinitic agglomerate at Oldoinyo Lengai comprises Sr-calcite, apatite, fluorite, a Ba-Mn oxide akin to romanrchite, and a distinctive Mn-Fe spinel. Formerly reported as sövite, on textural, mineralogical and stable isotope grounds it is now re-interpreted as a highly-altered natrocarbonatite lava. An implication of this study is that natrocarbonatite is not just a modern phenomenon, but has been extruded from Oldoinyo Lengai for at least around 1250 years.

The Kupferschiefcr contains from 0.3 to 30 wt.% of organic matter, with an average value close to 10 wt.%. The concentration of heavy metals increases strongly towards the base of a black shale horizon. Where the black shale rests directly on red sandstone, the bottom few mm of the shale may contain (ppm): Hg 8-1500, mean 174; Ag 310-5780, mean 1222; Au 1-3000, mean 40; Pd 2-1000, mean 37; Pt 2-340, mean 18. The shale, enriched in noble metals, is overlain by thucholite shale. The flotation sulphide concentrate contains 1-3 ppm Au and a detectable Pd and Pt content. Selected gravity concentrates from the black shale contain 4-56 ppm Au, up to 25 ppm Pd, while the Pt content does not exceed 1 ppm. A tightly intermixed clay-organic matrix of the noble metal-bearing shale contains small accumulations of Au, Pt and Pd presumably as organomctallic compounds.

Thucholite is present locally. It contains inclusions of uraninite, brannerite and noble metal minerals lcoated at the boundary between optically isotropic and anisotropic components. The optically homogeneous organic matrix of the thucholite contains discrete inclusions of UO2, brannerite, electrum and organic compounds of Au, U, Pt and Ni varying in size from 0.008 to 0.025 μm as shown by TEM. Gold occurs in a continuous Au-Ag series. Refractory Au is present as substitutions in native silver and in the organic matrix of the shale and thucholite. Palladium forms several arsenides and sulphoarsenides. Refractory Pd is present as substitutions in Ni-Co arsenides and in the organic matrix of the shale and thucholite. Platinum is present as substitutions in the organic matrix of the noblemetal- bearing shale and thucholite.

The average detection limits of micro-PIXE were 8-10 ppm, and those of the SXRFA from one to a few ppm. A major factor defining detection limits in the studied samples were minor uranium lines overlapping spectral lines of the studied elements.

Three types of mafic granulites, namely two pyroxene-plagioclase granutite (MG), two pyroxeneplagioclase-garnet granulite (GMG) and spinel-olivine-plagioclase-two pyroxene granulite (SMG) are exposed at Sunkarimetta, Eastern Ghats belt, India. The marie granulites exhibit a foliation concordant with that in associated granulite facies quartzofeldspathic gneisses. Textural characteristics and mineral chemical data suggest the following mineral reactions: olivine + plagioclase = spinel + orthopyroxene + clinopyroxene (SMG), orthopyroxene + plagioclase = garnet + quartz (GMG), clinopyroxene + plagioclase = garnet + quartz (GMG) and plagioclase + hemoilmenite + quartz = garnet + ilmenite + 02 (GMG). Geothermobarometry indicates maximum P-T conditions of metamorphism at c. 8.5 kbar, 950°C The marie granulites later suffered nearly isobaric cooling to c. 7.5 kbar, 750°C Bulk compositional characteristics suggest that SMG is of cumulate origin. The protoliths of the mafic granulites, emplaced at c. 32 km depth, are probably responsible for thermal perturbation causing granulite facies metamorphism of the enclosing rocks.

Musgravite, Be(MgFeZn)2Al6O12, is associated with norbergite and minor chlorite in a Precambrian calcite marble within the gneissic basement in an internal part of the Caledonian mobile belt in Dove Bugt, North-East Greenland. It commonly occurs as vitreous black, idioblastic crystals (<7 mm in size) with combined rhombohedral and basal pinacoid forms. XRD data show that its space group is R3m and its unit cell dimensions are a 5.687 ± 0.002 Å and c 41.16 ± 0.02 Å. Electron microprobe and ICP-MS analyses have yielded BeO 5.51 wt.% and ranges in abundance (wt.%): Al2O3 68.74-70.63; Tot, Fe as FeO 6.76-7.89; MgO 12.17-13.98; and ZnO 3.22-4.47. ICP-MS analysis also revealed significant trace amounts of V 249 ppm, Cr 740 ppm and Ga 178 ppm. The crystallographic parameters and composition are broadly in accord with those of musgravite from the two other recorded occurrences, in Precambrian high-grade terrains in Australia and Antarctica, although mineral and rock associations in these localities differ from those in Dove Bugt. The source of beryllium in each of the musgravite occurrences is uncertain, although a metasomatic source related to granite emplacement is favoured for the occurrence in North-East Greenland.

Serpentinised ultramafic bodies containing zoned chromite grains occur in the Cordillera Frontal Range, western Argentina. Chromites show Zn-rich Al-chromite cores (4.04 wt.% ZnO) surrounded by ferritchromite rims (1.3 wt.% ZnO) and outer Cr-magnetite rims. In intensely altered chromites which are spatially related to sulphide mineralisation, the primary chromite cores have been replaced by Zn-rich ferritchromit (7 wt.% ZnO) and they are rimmed by Cr-magnetite. In the Al-chromites the mean [Cr/(Cr + Al] ratio is 0.53 and the [Mg/(Mg + Fe)] ratio is 0.53; they plot in the field of Alpinetype intrusions. Ferritchromit has a mean [Cr/(Cr + Al)] ratio of 0.93 and [Mg/(Mg + Fe)] ratio of 0.4. In Cr-magnetites the mean [Cr/(Cr + Al) is 0.98 and the [Mg/(Mg + Fe)] ratio is 0. Ferritchromit is always surrounded by a Cr-magnetite rim and it was formed as a reaction product owing to the irreversible dissolution of primary chromite cores. The dissolution of these cores provided the essential components for ferritchromit growth. Zn was introduced into the chromite cores and ferritchromit rims during the formation of the latter. Step-scan profiles have shown that the Zn content in the cores increases from the centre to their outer border, where they show the highest Zn values. It is suggested that Zn was introduced by the fluid phase involved in the alteration process that affected the cores and lead to the formation of the zoned chromite grains. This alteration process was also responsible for the changes in [Cr/(Cr + Al)] and [Mg/(Mg + Fe)] ratios.

The kinetics and reaction mechanisms of chlorite breakdown have been studied in a series of experiments at conditions similar to those achieved during contact metamorphism (T = 600-725°C P = 1 kbar). Cores of chlorite schist were used as starting material in order to simulate natural metamorphic systems and preserve reaction textures. Reaction products were analysed by electron microprobe, scanning- and transmission-electron microscopy (SEM, TEM). Although the texture of the original chlorite was preserved in experiments run below 680°C talc had replaced chlorite. Olivine and spinel formed along grain boundaries, indicating long-range diffusion of aluminium. Above 680°C the chlorite was replaced by patches of disordered, aluminous pyroxene. Olivine and spinel grew both within the pyroxene and along what are believed to be former chlorite grain-boundaries. Reactions relevant to the observed textures and assemblages are:

Thermodynamic calculations show that both of these reactions are metastable in the FeO-MgO-Al2O3-SiO2-H2O system in the P-T range of our experiments. In addition, previous experimental studies and our calculations indicate that the stable reaction is:

The absence of cordierite in the run products, and the formation of talc and orthopyroxene while thermodynamically metastable, show that the ease of nucleation of these phases controlled the reaction mechanisms in the early stages.

The crystal structure of KBSi3O8 (orthorhombic, Pnam, with a = 8.683(1), b = 9.253(1), c = 8.272(1) Å,, V = 664.4(1) Å3, Z = 4) has been determined by the direct method applied to 3- dimensional rcflection data. The structure of a microcrystal with the dimensions 20 × 29 × 37 μm was refined to an unweightcd residual of R = 0.031 using 386 non-zero structure amplitudes. KBSi3O8 adopts a structure essentially different from recdmergneritc NaBSi3O8, with the low albite (NaAlSi3O8) structure, and isotypic with danburite CaB2Si2Os which has the same topology as paracelsian BaAl2Si2O8. The chenfical relationship between this sample and danburitc gives insight into a new coupled substitution; K+ + Si4+ = Ca2+ + B3+ in the extraframework and tetrahedral sites. The present occupancy refinement revealed partial disordering of B and Si atoms which jointly reside in two kinds of general equivalent points, T(1) and T(2) sites. Thus the expanded crystal-chemical formula can be written in the form K(B0.44Si0.56)2(B0.06Si0.94)2O8

The systematic trend among crystalline compounds with the M+T3+T4+3O8 formula suggests that they exist in one of four structural types; the feldspar structures with T3+/T4+ ordered and/or disordered forms, and the paracelsian and the hollandite structures.