In 2002 a new dinosaur tracksite was discovered in calcareous laminites of early Late Kimmeridgian age along the future course of the "Transjurane" highway in Courtedoux, Canton Jura, Northern Switzerland. The site has an extraordinary scientific potential, as the laminites, which have been deposited in an intertidal to supratidal environment, contain at least 6 track-bearing levels in a total thickness of about 1 m. The laminites are being systematically excavated by the "Section de paleontologie" over an area of approximately 1500 m2. So far the main track level has been uncovered over an area of about 650 m2, which reveals 2 trackways of theropods and 17 trackways of sauropods. The sauropod tracks are the smallest known in the Kimmeridgian so far, and the trackways belong to the ichnogenus Parabrontopodus, which has been revealed for the first time in Switzerland. The tracksite belongs to the "Middle Kimmeridgian megatracksite" sensu Meyer (2000), and represents the most important dinosaur tracksite in Switzerland, perhaps with the potential for development into one of the world's largest sauropod tracksites. It will be protected in situ underneath an especially constructed highway-bridge, thus offering opportunities for future research and the development of an interpretative center for education and tourism.
Abstract: A new semionotiform fish, Isanichthys palustris gen. et sp. nov., is described from the Late Jurassic – Early Cretaceous Phu Kradung Formation, north‐east Thailand. I. palustris is known from a single, nearly complete specimen found alongside abundant Lepidotes specimens at the Phu Nam Jun locality. I. palustris shows a mixture of semionotid‐like characters, such as the pattern of cheek ossifications, and lepisosteid‐like characters, such as the body shape and a dorsal fin opposed by an anal fin. I. palustris possesses only some of the characters currently used to define the Semionotidae. Cladistic analyses including various semionotid and gar taxa, together with Amia calva and Leptolepis coryphaenoides , suggest that the Semionotiformes (Lepisosteidae and ‘Semionotidae’) form a monophyletic clade, but the ‘Semionotidae’ taxa form an unresolved polytomy. The relationships between Semionotiformes, Halecomorphi and Teleostei are unresolved. When restricted to the best‐known taxa, however, the analysis shows the monophyly of the Semionotidae sensu stricto ( Semionotus + Lepidotes ) and a sister‐group relationship between halecomorphs and teleosts. These last two results are regarded as the preferred hypothesis for further studies. I. palustris is the only known example of a predaceous, probably piscivorous, ‘semionotid’. It illustrates the great diversity and ecological adaptation of the semionotiforms during the Late Jurassic – Early Cretaceous. We question the phylogenetic relationships of ‘ancient fishes’ founded on molecular‐based trees because we suspect that the use of very few Recent taxa as representatives of previously diverse lineages is an inevitable, but important, bias in the construction of such trees.
Although the split of coelacanths from other sarcopterygians is ancient, around 420 million years ago, the taxic diversity and the morphological disparity of the clade have remained relatively low, with a few exceptions. This supposedly slow evolutionary pace has earned the extant coelacanth Latimeria the nickname “living fossil”. This status generated much interest in both extinct and extant coelacanths leading to the production of numerous anatomical studies. However, detailed descriptions of extinct taxa are made difficult due to the quality of the fossil material which generally prevents fine comparisons with the extant Latimeria . Here we describe a new genus and species of coelacanth, Graulia branchiodonta gen. et sp. nov. from the Middle Triassic of Eastern France, based on microtomographical imaging using synchrotron radiation. Through exquisite 3D preservation of the specimens, we reconstructed the skeletal anatomy of this new species at an unprecedented level of detail for an extinct coelacanth, and barely achieved for the extant Latimeria . In particular, we identified a well-developed trilobed ossified lung whose function is still uncertain. The skeletal anatomy of G . branchiodonta displays the general Bauplan of Mesozoic coelacanths and a phylogenetic analysis resolved it as a basal Mawsoniidae, shedding light on the early diversification of one of the two major lineages of Mesozoic coelacanths. However, despite its exquisite preservation, G . branchiodonta carries a weak phylogenetic signal, highlighting that the sudden radiation of coelacanths in the Early and Middle Triassic makes it currently difficult to detect synapomorphies and resolve phylogenetic interrelationships among coelacanths in the aftermath of the great Permo-Triassic biodiversity crisis.
Coelacanths are iconic fishes represented today by a single marine genus. The group was a little bit more diversified in the Mesozoic, with representatives in marine and continental environments in the Late Cretaceous. Here we describe isolated skull bones of the last know freshwater coelacanths found in several fossil sites from the Early Campanian to the Early Maastrichtian of Southern France (in the Departments of Aude, Bouches-du-Rhône, Hérault, and Var). The sample does not allow distinguishing different species, and all material is referred to Axelrodichthys megadromos Cavin, Valentin, Garcia originally described from the locality of Ventabren in Southern France. A reconstruction of the skull is proposed. Previously unrecognized features are described, including parts of the postparietal portion of the skull, of the suspensorium and of the mandible. The new data confirm the assignation of the species to the mawsoniids, and more specifically to Axelrodichthys. A cladistic analysis scoring new character states provides a similar topology than a previous analysis, i.e. A. megadromos is placed in a polytomy with Axelrodichthys araripensis and Lualabaea lerichei, two species from the Early Cretaceous of Brazil and from the Late Jurassic of the Democratic Republic of the Congo, respectively. A. megadromos appears to have been restricted to freshwater environments, to the contrary of oldest Western Gondwanan representatives of the family that were able to live in brackish and marine waters. A. megadromos is the last representative of the mawsoniids and its occurrence in Europe is probably the result of a dispersal event from Western Gondwana that happened somewhen in the Cretaceous. Based on the available data, the mawsoniids went extinct in the mid-Maastrichthian, i.e. before the end-Cretaceous mass extinction. But it is possible that the fossil record of this family, which has been only recently recognized in Late Cretaceous European deposits, will geographically and stratigraphically widen with further discoveries.
ABSTRACT †Siamamia naga, gen. et sp. nov, is described on the basis of three partly articulated skulls and a collection of isolated ossifications from a continental Early Cretaceous Formation of northeastern Thailand. The new taxon is a †sinamiid halecomorph as demonstrated by the median parietal and other cranial characters. †Sinamiidae is hitherto known by two genera occurring in Early Cretaceous freshwater deposits in China. Although a complete revision of all species within the family is necessary, the Thai material shows characters justifying a new genus. It is the first †sinamiid found outside eastern Asia (South and North Chinese blocks, plus small Central Asian terranes), thus validating the close paleogeographical affinities between mainland Asia and SE Asia in the Early Cretaceous. A preliminary phylogenetic assessment of the new taxon with the data matrix of Grande and Bemis (1998) with the addition of data for †Siamamia and †Tomognathus provides a strict consensus tree similar to the phylogenetic hypothesis of Halecomorphi proposed by these authors, except the basal-most amiids which show a lower resolution in our hypothesis. The †Sinamiidae appear as a monophyletic clade, but the four taxa included in the analysis form a polytomy.
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