Postcranial remains of the Russian Late Devonian tetrapod Tulerpeton include the hexadactylous fore limb, hind limb, anocleithral pectoral girdle, squamation, and associated disarticulated postcranial bones. A cladistic analysis indicates that Tulerpeton is a reptiliomorph stem‐group amniote and the earliest known crown‐group tetrapod: Acanthostega and Ichthyostega are successively more derived plesion stem‐group tetrapods and do not consititute a monophyletic ichthyostegalian radiation. Previous analyses suggesting a profound split in tetrapod phylogeny are thereby corroborated, and likewise the interpretation of Westlothiana as a stem‐group amniote. The divergence of reptiliomorphs from batrachomorphs occurred before the Devonian‐Carboniferous boundary. Tulerpeton originates from an entirely aquatic environment with a diverse fish fauna. The morphologies of its limbs and those of Devonian stem‐tetrapods suggest that dactyly predates the elaboration of the carpus and tarsus, and that Polydactyly persisted after the evolutionary divergence of the principal lineages of living tetrapods. The apparent absence of a branchial lamina and gill skeleton suggests that Tulerpeton was primarily air‐breathing, whereas contemporary stem‐group tetrapods and more recent batrachomorphs retained greater emphasis on gill‐breathing.

Ventastega curonica, from the Upper Famennian Ketleri Formation, is the first tetrapod find from the Upper Devonian of Latvia, and only the fourth adequately represented Devonian tetrapod genus to be described. The taxon is represented by disarticulated cranial and postcranial elements from two localities, Ketleri on the Venta River and Pavari on the Ciecere River. A second tetrapod, represented by a single mandibular fragment, appears to be present at Ketleri. The lower jaw of Ventastega is strikingly primitive in retaining fangs on the coronoid series, but shares many characters with those of other known Devonian tetrapods. Some of these features are interpreted as basal tetrapod synapomorphies; they provide a new data set for the identification of isolated tetrapod jaw fragments, and confirm the (previously disputed) tetrapod status of Metaxygnathus. The upper jaw bones of Ventastega are broadly similar to those of Acanthostega, Ichthyostega and Tulerpeton, as is the narial region. The lateral rostral bone is either very small or absent. A preopercular bone is present in the cheek, and the lacrimal is excluded from the orbit. The palate is closed. Palatine and vomer bear fangs which are set in the marginal tooth row. An isolated iliac blade from Pavari, probably attributable to Ventastega, resembles that of Acanthostega but may not have carried a dorsal process. Two clavicles from Pavari and Ketleri which may also belong to Ventastega are of a typical early tetrapod pattern, similar to Greerpeton but with a broader ventral blade. Non-attributable or doubtfully attributable bones from Ketleri include a probable tetrapod postorbital and a possible limb bone. Ventastega appears to be a tetrapod of the same broad `grade' as Ichthyostega and Acanthostega, but is arguably more primitive than either.

BackgroundThe pituitary gland is formed by the juxtaposition of two tissues: neuroectoderm arising from the basal diencephalon, and oral epithelium, which invaginates towards the central nervous system from the roof of the mouth. The oral invagination that reaches the brain from the mouth is referred to as Rathke’s pouch, with the tip forming the adenohypophysis and the stalk disappearing after the earliest stages of development. In tetrapods, formation of the cranial base establishes a definitive barrier between the pituitary and oral cavity; however, numerous extinct and extant vertebrate species retain an open buccohypophyseal canal in adulthood, a vestige of the stalk of Rathke’s pouch. Little is currently known about the formation and function of this structure. Here we have investigated molecular mechanisms driving the formation of the buccohypophyseal canal and their evolutionary significance.ResultsWe show that Rathke’s pouch is located at a boundary region delineated by endoderm, neural crest-derived oral mesenchyme and the anterior limit of the notochord, using CD1, R26R-Sox17-Cre and R26R-Wnt1-Cre mouse lines. As revealed by synchrotron X-ray microtomography after iodine staining in mouse embryos, the pouch has a lobulated three-dimensional structure that embraces the descending diencephalon during pituitary formation. Polarisfl/fl; Wnt1-Cre, Ofd1-/- and Kif3a-/- primary cilia mouse mutants have abnormal sonic hedgehog (Shh) signaling and all present with malformations of the anterior pituitary gland and midline structures of the anterior cranial base. Changes in the expressions of Shh downstream genes are confirmed in Gas1-/- mice. From an evolutionary perspective, persistence of the buccohypophyseal canal is a basal character for all vertebrates and its maintenance in several groups is related to a specific morphology of the midline that can be related to modulation in Shh signaling.ConclusionThese results provide insight into a poorly understood ancestral vertebrate structure. It appears that the opening of the buccohypophyseal canal depends upon Shh signaling and that modulation in this pathway most probably accounts for its persistence in phylogeny.

Lebedev, O.A., Mark-Kurik, E., Karataj u t E -Talimaa, V.N., Luk ß evi ç s, E. and Ivanov, A. 2009. Bite marks as evidence of predation in early vertebrates. -Acta Zoologica (Stockholm), 90 (Suppl. 1): 344-356Study of lifetime bite traces on agnathans and fish (or gnathostomes) from Ukraine, Estonia, Latvia and north-western and central European Russia reveals evidence of predator-prey relationships in communities of Devonian age. Numerous bite traces on skeletal parts of agnathan pteraspidiforms and psammosteiforms, placoderm arthrodires and antiarchs and sarcopterygian porolepiforms and osteolepiforms are described. Evidence of healing shows that prey organisms responded to predation by reconstruction of damaged skeletal elements. Ichthyofaunistic analysis is used to establish possible predators. The most probable predators in the Middle and Late Devonian communities are sarcopterygian porolepiforms and osteolepiforms. Predatory tetrapods become evident during the Famennian. Global analysis of aquatic predators during the Silurian-Devonian interval shows a gradual increase in species numbers with time. During the Late Silurian, only ischnacantid acanthodians, early osteichthyans and sarcopterygians are known to belong to this trophic group. By the end of the Devonian this list is complemented by chondrichthyans, arthrodires, porolepiform, osteolepiform, struniiform and rhizodontiform sarcopterygians and tetrapods. Only Devonian agnathans show no predatory groups. In sarcopterygians, predatory dentitions, which developed according to more or less the same pattern, show little change during the Devonian.

Lebedev, O.A. 2009. A new specimen of Helicoprion Karpinsky, 1899 from Kazakhstanian Cisurals and a new reconstruction of its tooth whorl position and function. -Acta Zoologica (Stockholm) 90 (Suppl. 1): 171-182A new Helicoprion bessonowi Karpinsky, 1899 (Chondrichthyes, Eugeneodontiformes) specimen from the Artinskian of Kazakhstan is described. This is the southernmost occurrence of this species in the Cisurals area. Its presence suggests a biogeographical link for this species between the Cisurals and Japan. Residue obtained from chemical preparation of the sample included numerous scales and several teeth, which are tentatively assigned to Helicoprion . This assumption is based upon morphological similarity of the scales to those known in other eugeneodontiforms. Campodus -like teeth might be part of the lateral dentition of Helicoprion . A new reconstruction of the interaction of the lower tooth whorl with the upper jaw dentition is suggested and its function is discussed. It is proposed that there was no symphysial whorl in the upper jaw but its role was played by a rigid cover formed by a series of small teeth at the palatoquadrates. Microscopic study of the tooth crown surface revealed scratch marks, which might have resulted from pressing the food object against the upper jaw. Using extant odontocetans as an ecological model led to a conclusion that helicoprionids most likely fed on cephalopods and to some extent on fish. This assumption is based upon the concentration of functional dentition in the area of the lower jaw symphysis in both groups of animals.