The presence of a petaloid pattern (previously known as ‘dark dentine’) in cross sections of teeth of the embolomere Pholiderpeton attheyi has been used as a synapomorphy of the embolomeres or of the embolomeres plus the stem tetrapod, Crassigyrinus scoticus. Among the taxa studied, dentine that appears dark results from closely packed dentine tubules and can be found in any part of a tooth section in which such crowding occurs. The petaloid pattern is restricted to tooth sections of a particular diameter, and is obliterated in larger sections of teeth that show complex folding. Petaloid dentine has been found in all tetrapod teeth with plicidentine that were sectioned in this study, whether from stem tetrapods, the Embolomeri, Temnospondyli, or Stereospondyli, and has been recognised in some sarcopterygian fish, an extant actinopterygian fish, ichthyosaurs, and Varanus. The presence of petaloid dentine is neither a synapomorphy of the tetrapod node nor of any node within tetrapods

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.

Devonian rhizodontid fishes from East Gondwana include Gooloogongia loomesi Johanson & Ahlberg 1998 from near Canowindra, New South Wales (NSW), Australia and Aztecia mahalae gen. nov., sp. nov. from southern Victoria Land, Antarctica. Gooloogongia loomesi is known from well-preserved cranial and postcranial material, and as such represents the most complete rhizodont known. Newly discovered elements (braincase, pelvic girdle) are described for the first time. Aztecia mahalae gen. nov., sp. nov. is based on shoulder girdle material formerly assigned to Notorhizodon Young et al. 1992, which, based on skull and lower jaw morphology, is a member of the Tristichopteridae. The presence of several plesiomorphic characters suggests that Gooloogongia occupies a basal phylogenetic position within the Rhizodontida, while Aztecia n. gen. possesses a more derived shoulder girdle. We argue that the Rhizodontida evolved on the Gondwanan landmass. Notorhizodon occupies a relatively derived position within the Tristichopteridae, but is contemporary with the earliest and phylogenetically most basal Laurussian members of the group. This shows that the tristichopterids achieved a worldwide distribution considerably earlier than previously thought.