Xenacanthids were a very successful group of elasmobranchs that ranged from the Lower Carboniferous to the Upper Triassic. The history of discovery of the xenacanthids, which is closely connected with the history of coal prospecting in England, began with the finding of the type specimen of Xenacanthus laevissimus in the Westphalian B of the West Midlands. In this first review of British Carboniferous xenacanthids, the number of taxa, mainly erected during Victorian times, is reduced to 14 species distributed among six genera. Determinable remains are recorded from at least 96 localities in the British Isles. Unique characteristics of the Dinantian Diplodoselache suggest that the lineage to which this taxon belongs marks a dead end in xenacanthid evolution. This investigation also shows that the Pendleian Dicentrodus, formerly described as Cladodus, belongs to the xenacanthids. The occurrence of Orthacanthus cf. kounoviensis in the Pennines, also known from the German Saar-Nahe basin, the Saale depression and from Bohemia, indicates a faunal exchange between these intramontainous basins during the Carboniferous. The genus Triodus is identified from British deposits for the first time. A cladistic analysis of the xenacanthids suggests that they evolved from phoebodontid elasmobranchs. This analysis also confirms separation of the Middle Devonian Antarctilamna from a relationship with xenacanthid sharks.

Tertiary–Recent magmatism in the Kenya Rift Valley was initiated c. 35 Ma, in the northern part of Kenya. Initiation of magmatism then migrated southwards, reaching northern Tanzania by 5–8 Ma. This progression was accompanied by a change in the nature of the lithosphere, from rocks of the Panafrican Mozambique mobile belt through reworked craton margin to rigid, Archaean craton. Magma volumes and the geochemistry of mafic volcanic rocks indicate that magmatism has resulted from the interaction with the lithosphere of melts and/or fluids from one or more mantle plumes. Whilst the plume(s) may have been characterised by an ocean island basalt-type component, the chemical signature of this component has everywhere been heavily overprinted by heterogeneous lithospheric mantle. Primary mafic melts have fractionated over a wide range of crustal pressures to generate suites resulting in trachytic (silica-saturated and-undersaturated) and phonolitic residua. Various Neogene trachytic and phonolitic flood sequences may alternatively have resulted from volatile-induced partial melting of underplated mafic rocks. High-level partial melting has generated peralkaline rhyolites in the south–central rift. Kenyan magmatism may, at some future stage, show an increasing plume signature, perhaps associated ultimately with continental break-up.

The Rhizodontida (Pisces: Sarcopterygii) is a clade of predatory fishes from the Upper Devonian (Aztecia; ?Givetian of Antarctica) through to the Upper Carboniferous (Strepsodus; Moscovian of northern Europe and North America). They form the most basal plesion within the tetrapod stem-lineage. The mandibles were dominated by large symphysial tusks on the dentary. Not much else is known of the mandibles in primitive rhizodontids. However, later forms show several derived characters: the mandible is very deep dorsoventrally and narrow linguolabially; the coronoid fangs bear only a single fang and no other dentition; the Meckelian element was unossified, leaving the adductor fossa unfloored by bone; the prearticular produced a large dorsal process lingual to the adductor fossa, presumably for muscle attachment. These and other characters are discussed in the context of the evolution of the tetrapod stem-group.

The mandible appears to have been split into two functional units, one comprising the firmly sutured prearticular, coronoids and dentary, the other comprising the firmly sutured infradentaries. The connection between the two units was weak, suggesting a longitudinal intramandibular hinge. The possibility that this acted as a ‘torsion grip’ during feeding is discussed.

Abundant microvertebrate remains from the Siberian Platform are described as early acanthodians. All are preserved with both excellent morphology and histology. They are assigned to a new order, Tchunacanthida, with two new families, Lenacanthidae and Tchunacanthidae. These comprise two new genera, Lenacanthus and Tchunacanthus with type species L. priscus sp. nov. and T. obruchevisp.nov. The evidence from the morphology and histology is that they are the most ancient acanthodian scales so far found. The total collection of vertebrate material from the Irkutsk amphitheatre is described, together with their geological distribution, geographical range and systematic palaeontology. Head scales, tesserae of three morphotypes, transitional scales and body scales have been found. All comprise morphological sets as determined by comparison of morphology using SEM and of histology using Nomarsky interference optics. Observations of growth were possible from details of concentric lines on the crown and also from incremental layers seen in both horizontal and vertical sections. Starting from the primordial scale, consecutive layers are added, coronally, laterally, and deep in the corium onto the base; these occurred simultaneously in both crown and base. A type of areal-superpositional growth occurred in some body scales but in other scales there was little superpositional growth. It is concluded that Tchunacanthus possessed very solid body armour with tightly joined scales covering a large area of the body, and scale bases deeply set in the corium. Both tissues of the scales, dentine and bone, feature enclosed cells. This character is regarded as primitive within acanthodians, as in derived forms both tissues are acellular. Acanthodian scales are one of many examples of transformation from cellular to acellular tissue in evolution.