Foraminifers, calcareous algae and incertae sedis Algospongia of late Asbian to late Brigantian age in limestones from East Fife, East Lothian and Northumberland, enable the base of the late Brigantian to be recognised in all these areas. Preservation of the late Asbian and early Brigantian limestones in cyclothemic successions is generally poor. The St Monans White Limestone (St Monans, Fife), First Abden Limestone (Kirkcaldy, Fife), Middle Longcraig Limestone (East Lothian) and Lower Bath-House Wood/Middle Bath-House Wood (Northumberland) were confidently correlated by their foraminiferal assemblages. These limestones are all assigned to the top of the Assemblage 6 in northern England (Single Post Limestone). The St Monans Brecciated/St Monans Little/Charlestown Main limestones (St Monans, Fife) and the Second Abden/Seafield Tower limestones (Kirkcaldy, Fife), Upper Longcraig/Lower Skateraw limestones (East Lothian), Upper Bath-House Wood/Shotto Wood limestones and Eelwell Limestone (Northumberland) are assigned to the Assemblage 7 in northern England (Scar Limestone and Five Yard Limestone). The paired Middle/Upper Skateraw limestones (East Lothian) and the Acre Limestone (Northumberland) contain representatives of the Assemblage 8 from northern England (Three Yard Limestone). Higher up in the succession, in Northumberland, the foraminiferal assemblage in the Sandbanks Limestone can be compared with Assemblage 9 in northern England (Four Fathom Limestone). Above the Great Limestone and Little Limestone, with their characteristic Pendleian assemblages, the Sugar Sands Limestone and Corbridge Limestone contain Arnsbergian foraminiferal assemblages, typical of the Lower Felltop Limestone in northern England. The Lower Foxton Limestone is correlated with the Upper Felltop Limestone, whereas the Thornbrough Limestone in Northumberland lacks diagnostic Arnsbergian taxa.

The Permo-Carboniferous eurynotiforms show conspicuous modifications to postcranial and cranial morphology relative to primitive actinopterygian conditions, and represent an important early example of functional experimentation within ray-finned fishes. Although eurynotiforms are represented by abundant articulated fossil material, the internal anatomy of the group is not well known. Microcomputed tomography (μCT) of Eurynotus crenatus from the early Carboniferous (Viséan) Wardie Shales Member of the Gullane Formation of Wardie, Scotland provides detailed information on the jaws, palate and dentition. The lower jaw is deep and bears a well-developed convex dental plate on the prearticular/coronoids. The dentary bears a dorsally directed posterior process and lacks any obvious marginal dentition. The prearticular bears a low coronoid process. Apart from the first and second dermopalatines, and a likely accessory vomer, bones of the palate are tightly sutured or fused. The upper dental plate comprises a longitudinal, concave horizontal dental surface that occludes with the convex lower toothplate, and a more vertical region consisting of anastomosing ridges. The parasphenoid has a narrow anterior corpus and a broad posterior stalk that bears a pronounced midline notch. The smooth, irregularly punctated surfaces of the dental plates are formed by closely packed teeth with conjoined crowns, providing clues to the evolution of the more monolithic toothplates of Amphicentrum from the peg-like teeth reported in the earliest and most anatomically generalised eurynotiforms. The feeding apparatus shows many qualitative and quantitative features consistent with the processing of hard prey items. Eurynotus and its relatives show the first clear example of jaw and dental structures consistent with durophagy among actinopterygians. The origin of the group in the early Carboniferous is suggestive of diversification into newly available ecological roles in the aftermath of the end-Devonian extinction.

Two new species of Schramocaris from the Viséan, Lower Carboniferous of Scotland and eastern Canada extend the range and distribution of this crustacean along the northwestern coast of the Rheic Ocean. New species from Glencartholm, southern Scotland and Upperton, New Brunswick, Canada represents the first recognised occurrence of this genus in Scotland and Canada. The Scottish species is here named S. clarksoni; it lacks the rugosity of the carinae of Schramocaris gilljonesorum, but has the same relative position of the carinae, as well as similar characteristics of the pleon, such as the relative lengths of the somites and the shape of the telson. The Canadian species is named Schramocaris matthewi on the basis of the papillations on the cuticle and robust second carinae of the carapace. The deposits at both these localities are that of a shallow marine argillaceous environment, although the Glencartholm deposit contains more lime. Schramocaris has previously only been known from the Avon Group (Hastarian) of the Forest of Dean, England.

A revision of the Carboniferous lungfish genus Ctenodus is undertaken. Ctenodus is the longest-surviving genus of lungfish from the Carboniferous, and is the only one to cross the Lower–Upper Carboniferous boundary. Five species span the period, with species correlated to stage. Species are distinguished by differences in tooth plate morphology. Ridge number increases from the Tournaisian to the Moscovian, and the length to width ratio decreases. A new, almost complete articulated individual of C. interruptus allows identification of this species from pterygoid tooth plates and other characteristics. These, and new features of the postcranial skeleton, are described for the first time. Ctenodus retains primitive features of the skull roof, such as a pair of C-bones and retention of a D-bone; its contemporaries Conchopoma, Sagenodus and Straitonia show the derived condition of these features. Ctenodus retains primitive features of the lepidotrichia, which are distally segmented and bifurcated. However, it also shows the derived condition of the tail region in having a combined first and second dorsal fin: whether there was a separate caudal fin remains unknown.

The stem tetrapod Eucritta melanolimnetes is described in full from five specimens. The animal is compared in detail with the contemporary and superficially similar temnospondyl Balanerpeton woodi, and with baphetids (=loxommatids). Growth of Eucritta skulls approaches isometry, and lies on the same trajectory as skulls belonging to the genus Baphetes. The function of the temporal embayment is discussed; it was probably not associated with an air-borne hearing device. The axial skeleton of Eucritta was ossified in larger specimens. Ribs in Eucritta gain expanded distal ends with growth, and the animal probably breathed by buccal pumping. An updated cladistic analysis is presented, incorporating data from a fifth specimen. Eucritta remains as a probable basal baphetid, but the sister group to the baphetids remains uncertain.

Forty-one specimens of acanthodians and actinopterygians were examined from Units 26 to 38 of the Geikie Tuff, Little Cliff Shale and East Kirkton Limestone of the Viséan East Kirkton Limestone sequence. The results yielded six actinopterygian species including a platysomid and two probable juveniles of uncertain affinities, and three acanthodians including two acanthodidids and a climatiid-like denticle. Most specimens consist of isolated bones and scales, but articulated remains of an acanthodian and actinopterygians were found in Units 37 and 38 of the East Kirkton Limestone. The faunal composition is characteristically Oil-Shale in aspect and resembles that of Broxburn (Pumpherston). The presence of deep-bodied and juvenile fishes in the same strata combined with the mode of preservation indicate a palaeohabitat with limited current action and a soft substrate.

The hibbertopteroid eurypterid genera Hibbertopterus, Dunsopterus, and Cyrtoctenus occur in the East Kirkton Limestone of Bathgate, West Lothian. Most specimens are fragmentary and appear to have been washed into the depositional area with plant debris and tuffaceous sediment. Nearly all of the identifiable material can be attributed to Hibbertopterus scouleri (Hibbert), but two isolated Cyrtoctenus combs, and a femur comparable with Dunsopterus have also been recognised.

New material of Hibbertopterus scouleri (Hibbert) reveals that the posterior legs and telson resemble those of the cyrtoctenids more closely than was previously thought. It is possible that Hibbertopterus, Dunsopterus, and Cyrtoctenus are indistinguishable except by relatively minor characteristics, and that all of the material from East Kirkton Quarry might be derived from a single eurypterid species. However, associations of the diagnostic sclerites which would demonstrate that these taxa are either cogeneric or distinct have not yet been found.

Thirteen fragments of fossil elasmobranchs can be identified with certainty from East Kirkton. Those collected in situ range from Units 32 to 37. The remains appear to come from two different families of sharks: spines which show features typical of the Lower Carboniferous hybodont Tristychius arcuatus Agassiz; teeth from a xenacanth which fall within the size range of those found in the Lower Carboniferous xenacanth Diplodoselache woodi Dick. Both these genera are found in other Oil-Shale assemblages in the Lothians. These rare shark fossils reinforce the evidence that the East Kirkton Limestone was fresh water in origin.

Plant fossils are a common and important element in the East Kirkton biota of Brigantian (late Viséan age). The most important taxa are preserved as compressions or anatomically preserved as permineralisations. The basis of the quantitative study of the flora and the distribution of individual plant species was the trenched section excavated for the East Kirkton Project. The largest diversity of compressions have been recorded from loose blocks. In the trenched section, the uppermost ashes contain only lycopsid compressions including Stigmaria. Nodules in the underlying shales yield mainly lycopsid leaf and sporophyll compressions. The uppermost limestones (Units 39-52) contain drifted fragments of pteridosperm fronds mainly Sphenopteridium crassum, S. pachyrrhachis, Spathulopteris obovata and Adiantites antiquus. Permineralised Lyginorachis spp. occur at this level. Large permineralised woody gymnosperm axes have been found loose (including Pitus, 50 cm in diameter). Permineralised axes, mainly reworked, including the gymnosperms Bilignea, Eristophyton, Stanwoodia and possibly Protopitys, have been found in Units 72-88. Poorly preserved permineralised lycopsids are rare, but include Lepidophloios. Loose chert blocks contain root mats of permineralised Stigmaria, together with Lepidocarpon, the sphenopsid Archaeocalamites and the fern Botryopteris. Similar material is found in Unit 83 of the Limestone sequence. Unit 82, the black shale containing many of the articulated vertebrates, contains predominantly pteridosperm frond and pinnule material including Spathulopteris obovata. The distinctive changes in the flora from the base to the top of the trenched sequence reflect mainly ecological and taphonomic controls upon plant distribution and preservation. Evidence suggests a close relationship between climate, fire, erosion, deposition and vegetation type through the sequence and a climatic change, from a drier to a wetter environment, is suggested at the top of the East Kirkton Limestone sequence.

Silvanerpeton miripedes gen. et sp. nov. is a small gracile anthracosauroid. The holotype is an almost complete articulated specimen in black shale. Its anthracosaur characters include tabular-parietial contact, with a tabular horn and a moderate surangular crest indicating relationship with the embolomeres. It has gastrocentrous vertebrae with poorly ossified centra and neural arches, and the presacral vertebral count is estimated to be over 30. There are a number of apparently primitive characters as found in other anthracosauroids include a closed palate, mobile basal articulation, and an intertemporal. It differs from the other recognised species of anthracosaur at East Kirkton, Eldeceeon rolfei, in vertebral count, number of ribs, interclavicle shape, relative limb length, and in having an unossified tarsus, and a pedal phalangeal count of 23455.

Disarticulated bones from East Kirkton including large limb and vertebral elements may belong to this taxon, to Eldeceeon rolfei or to as yet unidentified taxa.

Several specimens of myriapodous arthropods have been discovered at the early Carboniferous East Kirkton site near Bathgate, West Lothian, Scotland. None is particularly well preserved, but they are the earliest known Carboniferous myriapods, filling the time gap between the Old Red Sandstone of the early Devonian and the abundant myriapod faunas of the late Carboniferous (Pennsylvanian). One of the specimens, a milliped, provides the earliest evidence for both ozopores (repugnatorial gland openings) and spiracles. A second milliped specimen has some characteristics of the living Order Glomeridesmida, and hence of Enghoff's (1990) ‘ground plan’ of chilognathan millipeds. Aspects of these forms and a third suggest a novel early Carboniferous fauna clearly different from both earlier and later ones. The taxon name ‘Myriapoda’ should be abandoned, since it covers a group now recognised as paraphyletic. ‘Archipolypoda’ is probably synonymous with Order Euphoberiida, Class Diplopoda.

A new fossil elasmobranch from the Lower Carboniferous Oil Shale groups (Viséan) of the Edinburgh area shows a mosaic of characters typical of at least two groups of early sharks. Its most distinctive feature is the small bicuspid teeth of “Diplodus” type. This, together with the long dorsal fin and the structure of the single, shallowly inserted dorsal spine, form a suite of characters previously considered unique to late Palaeozoic xenacanth sharks. Other features, such as the large equilobate tail and the structure of the pectoral fins, may have been retained from an ancestor of a more typical Palaeozoic elasmobranch appearance found in anacanthous and ctenacanth sharks. It is suggested that the xenacanths evolved from an ancestor within the anacanth-ctenacanth assemblage early in Carboniferous times and became adapted to a freshwater environment. This ancestor probably possessed a complex dermal skeleton including growing scales with both thickened and thin concave bases.

The fauna of the fish-bearing nodules amongst which this shark has been found is interpretedas being lagoonal in origin. The shark was probably a medium sized (c. 0·75–2·0 m lng)predator inhabiting the surface waters of the lagoon.