The axial skeleton and fin supports of the Middle Devonian lungfish Dipterus are described from a range of specimens from the Orcadian Basin of Scotland. The axial skeleton of the trunk region consists of intercentra, relatively short ribs, and neural arches bearing two rows of supraneural spines; posteriorly, the intercentra are replaced by haemal arches. The notochord seems to have been essentially unconstricted. There may have been two pairs of cranial ribs. In general terms the vertebral column resembles that of Neoceratodus but is more fully ossified. The only known paired fin support of Dipterus is an archipterygial structure resembling those of Neoceratodus, with at least seven mesomeres and jointed pre- and postaxial radials. The pectoral fin is rotated as in modern lungfishes. The median fin supports all consist of basal plates supporting radials. In the posterior dorsal fin support the posterior radials form a branched structure. The heterocercal tail is supported by segmental radials. A new body reconstruction is presented.

The characters possessed by Dipterus offer support for a lungfish–porolepiform sistergroup relationship. All known lungfishes fit into a single cumulative series of postcranial morphologies. The evidence for a paedomorphic trend in lungfish phylogeny is interesting but inconclusive.

The trace fossils of the Tumblagooda Sandstone (?late Silurian) of Kalbarri, Western Australia are spectacular in their variety and preservation. They provide a unique insight into the activities of the early invaders of terrestrial environments, and reveal the presence of a diverse fauna dominated by arthropods. Within the Formation trace fossil assemblages can be related to fluvial, aeolian and marine sand-dominated environments. Two distinct and diverse ichnofaunas are recognised.

The Heimdallia–Diplichnites Ichnofauna occurs in sandstones deposited in broad low sinuosity braided fluvial channels, between which were mixed aeolian and waterlain sandsheets, small aeolian dunes and flooded interdune and deflation hollows. Heimdallia is the major bioturbator, favouring shallow pools. Other burrows include Tumblagoodichnus (gen. nov.), Diplocraterion, Skolithos, Beaconites and Didymaulyponomos. Arthropod trackways (Diplichnites) occur on surfaces of waterlain sands and on foreset bedding of aeolian dunes, and represent some of the earliest reported terrestrial trackways. Other trackways include Paleohelcura and Protichnites, and the digging traces Selenichnites and Rusophycus are also present. At least ten types of arthropods are required to produce the observed traces. Myriapods, eurypterids, euthycarcinoids, xiphosurids and scorpionids are considered responsible for the trackway assemblage.

The Skolithos–Diplocraterion Ichnofauna occurs at the top of the exposed section in sandstones that overlie a thick fluvial sequence containing few traces. The strata are considered to represent marine influence at a fluvial/marine transition. They show variable trough cross-bedding, complex planar cross-bedding with down-climbing sets, ripple lamination, and fining-up sequences with bioturbated tops. Traces are dominated by crowded Skolithos up to 1 m long, together with two forms of Diplocraterion. Daedalus and Lunatubichnus (gen. nov.) burrows occur in a few beds and Aulichnites trails cover some foreset surfaces of cross-bedding.

The trace fossils and the sedimentology of the Tumblagooda Sandstone bear a remarkable similarity to those of the lower part of the Taylor Group of Antarctica, which is probably Devonian in age. It is suggested that the two represent a similar age, stratigraphy, and range of environments on the margins of Gondwana. Large unvegetated fluvial outwash plains with variable aeolian influence were essentially coastal in character and fluvial/marine transitions occur in sand-rich environments. The animals responsible for the traces inhabited coastal areas but many could survive outwith marine influence, and arthropods responsible for some types of Diplichnites trackways walked out of water.

The rich diversity of trackways attributable to arthropods illustrate that the invasion of terrestrial environments by arthropods, particularly large forms, was well-established by the beginning of the Devonian. The basis of the food chain was algal and bacterial films which bound the surface sediment in freshwater pools.

Conodont elements from Scottish Carboniferous rocks have been reviewed for Colour Alteration Index(CAI) data, and most values range between 1 and 1·5. Assuming a local average geothermal gradient similar to that of today, the observed and predicted CAI values generally fit well. Only a few of the samples analysed were influenced by local igneous intrusives. The CAI range shown lies within the immature (early dry gas) to mature (perhapsmid-oil window) stages of hydrocarbon generation, and this suggests that burial maturation (where CAI values are 1-5) could account for locally generated oil, where this occurred away from igneous intrusions. Alkali-dolerite and tholeiitic intrusives are, however, widespread in the Midland Valley of Scotland, and an understanding of their thermal effects has implications for both coal and petroleum exploration. The insensitivity of conodonts to low temperatures is noted, and the relevance, application and potential of various other palaeothermometers is discussed. Locally, the qualitative study of spore colour (SCI) appears useful.

Mineralisation associated with Late Caledonian metaluminous granitoids in the Grampian Terrane has been investigated using stable isotope, fluid inclusion and mineralogical techniques.

A porphyry-stock-related style of mineralisation in the Grampian Terrane is characterised by a stockwork of veinlets and disseminations in dacite prophyries, consisting of quartz, dolomite, sulphides and late calcite, and well-developed wallrock alteration dominated by zones of phyllic, sericitic and propylitic alteration. On the basis of δ34S (+0·4±l·0‰), δ13C (−5·7‰ to + l·4‰) and δ18O (+10·8‰ to +19·9‰) it is likely that initial mineralising components were orthomagmatic with an input of external fluids during the later parageneses. Fluids were saline, boiling (up to 560°C), deficient in CO2, and ore deposition took place at depths of less than 3 km.

Plutonic-hosted mineralisation in appinites, diorites, tonalites and monzogranites is commonly represented by sporadic disseminations and occasional veins consisting of quartz, calcite and sulphides. Wallrock alteration is generally propylitic with phyllic vein selvages. Deposition from a cooling magma sourced fluid is indicated by δ34S (+2·6±l·5‰), δ13C (−7·2‰ to −4·5‰) and δ18O (+9·5‰ to + ll·8‰) data. Fluids were CO2-rich and of low salinity; inclusions were trapped below ≈460°C, and formed at estimated depths of 3–5 km.

Differences between these styles of mineralisation may due to multiple factors, the most important being the nature of the fluid: porphyry systems are dominated by greater volumes and much higher temperatures of hydrothermal fluids. Other controlling factors are likely to be the compositional characteristics of the melt source region, the mechanism of magma ascent, the level of emplacement, and the nature of the host metasediments. Variations in δ34S between the two groups are related, for the most part, to redox processes during magma and fluid genesis and not by crustal contamination.

Nolarge porphyry-related mineral deposits have been found in the Grampian Terrane, unlike those in Mesozoic and Tertiary continental margin environments. This is largely due to a combination of detrimental factors which massively reducesthe probability of economic mineralisation. These include the already metamorphosed nature of the host Dalradian, the absence of seawater (which entered many subduction-related magmatic systems), a poorly-developed system of deep faults (most deposits too deep to be influenced by surface-derived fluids), and the absence of supergene enrichment. The main processes which aid the concentration of mineralisation involve encroachment of external fluids (formation, meteoric and seawaters) into the magmatic system, but these fluids were largely absent from the Grampian host block at the time of granitoid intrusion.

The results of this study can be used in characterising the sources of fluids in sedimentary-hosted ore veins known (or considered) to be underlain by metaluminous granitoid batholiths, particularly in estimating the degree of magmatic fluid inputs into the vein systems: an example where this interaction has occurred (the Tyndrum Fault Zone) is discussed.