Pyritic slates from the late Precambrian, Middle Dalradian Argyll Group Easdale Slate Formation, contain mainly quartz, muscovite and chlorite with variable amounts of dolomite, albite and paragonite. Slates from Easdale Island and Cuan Ferry contain pyrite porphyroblasts with δ34S = + 12 to + 16‰. The pyrite grew during a post-tectonic retrogressive event at the expense ofpyrrhotine which formed during the main regional metamorphism of the Grampian orogeny by reduction of diagenetic pyrite. Slate from Oban contains abundant diagenetic framboidal pyrite and small syn-tectonic pyrite porphyroblasts with δ34S = +22‰. This pyrite was not all reduced to pyrrhotine on metamorphism so there was little retrogressive growth of pyrite. Metamorphism appears to have homogenized local (cm scale at least) isotopic inhomogeneities and preserved an average seawater-sulphate-sulphide isotopic fractionation value. Middle Dalradian seawater-sulphate had a δ34S value of about + 35‰, so the small fractionations are appropriate for bacteriogenic reduction in bituminous sediments, the heavier sulphide in the case of the Oban slate indicating more rapid reduction of sulphate. Lower Dalradian Appin Group, Ballachulish slate contains pyrite with δ34S = +15±2‰ and is best interpreted as forming in the same manner as the Easdale slates of Easdale Island and Cuan Ferry; the sharp increase in late Precambrian ocean-sulphate sulphur isotope signature from +15 to > +30‰ therefore occurred by Lower Dalradian Appin Group times.

An investigation into the relative stabilities and equations of state of stoichiometric FeS was conducted using first-principles pseudopotential calculations. These calculations were based on density functional theory and performed using ultrasoft Vanderbilt pseudopotentials within the generalized gradient approximation. We have identified four stable polymorphs of FeS along the 0 K isotherm as a function of pressure: troilite, an orthorhombic MnP-type structure, a monoclinic structure, and a CsCl-type structure. The calculated internal energy as a function of volume for each polymorph was fitted to 4th order logarithmic and 3rd order Birch-Murnaghan equations of state, yielding values for the bulk modulus, K, and its first and second derivatives with respect to pressure, K′ and K″. These equations of state may be used to characterize models of planetary cores.

An apparatus is described for the measurement of the rates of fast precipitation reactions. It consists of a T-tube, where reactants are added to the arms of the T, mixed rapidly at the junction, and the rates of disappearance of reactants or appearance of products are measured along the stem of the T. The geometry of the system results in a steady state being established in the apparatus, enabling detailed analysis of reaction progress. The apparatus has been used to investigate the kinetics and mechanism of iron sulphide precipitation reactions. It has enabled measurements to be made with relatively high precision and good accuracy of the first 130 ms of reaction time.

Pyrite textures are described and illustrated and stable S-isotope data are presented from the Alton (Gastrioceras listen) marine horizon of the Westphalian Lower Coal Measures, from sections near Penistone in central northern England, with the object of relating the paragenetic sequence of pyrite formation to the conditions of sediment deposition and diagenesis. The earliest diagenetic pyrite is dispersed as framboidal and related textures. It is followed in the marine shale, coal and ganister by more localised but more intense pyrite deposition and replacement in a variety of textures. Most of this is precompactional in age, but some, together with pyrite in veinlets and cleat, is postcompactional. Marcasite is rare and mainly late. δ34S ratios range between −35·31‰ and +20·39‰. There is a definite trend from lighter values (−1·15 ± 6·47‰) in the marine part of the sequence to much heavier values (+12·73 ± 7·66‰) in the sediment below the coal. This allows the relationship of the earliest pyrite deposition in the coal-peat and ganister to the chemistry of their own depositional fresh water to be seen but then relates the main pyrite deposition to the influx of the marine-water sulphate of the Alton horizon, and shows the penetration of this influence downward into the coal-peat and its seat-bed.