507 research outputs found

    The Osteology of the Basal Archosauromorph Tasmaniosaurus triassicus from the Lower Triassic of Tasmania, Australia

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    Proterosuchidae are the most taxonomically diverse archosauromorph reptiles sampled in the immediate aftermath of the Permo-Triassic mass extinction and represent the earliest radiation of Archosauriformes (archosaurs and closely related species). Proterosuchids are potentially represented by approximately 15 nominal species collected from South Africa, China, Russia, Australia and India, but the taxonomic content of the group is currently in a state of flux because of the poor anatomic and systematic information available for several of its putative members. Here, the putative proterosuchid Tasmaniosaurus triassicus from the Lower Triassic of Hobart, Tasmania (Australia),is redescribed. The holotype and currently only known specimen includes cranial and postcranial remains and the revision of this material sheds new light on the anatomy of the animal, including new data on the cranial endocast. Several bones are re-identified or reinterpreted, contrasting with the descriptions of previous authors. The new information provided here shows that Tasmaniosaurus closely resembles the South African proterosuchid Proterosuchus, but it differed in the presence of, for example, a slightly downturned premaxilla, a shorter anterior process of maxilla, and a diamond-shaped anterior end of interclavicle. Previous claims for the presence of gut contents in the holotype of Tasmaniosaurus are considered ambiguous. The description of the cranial endocast of Tasmaniosaurus provides for the first time information about the anatomy of this region in proterosuchids. The cranial endocast preserves possibly part of the vomero-nasal (= Jacobson's) system laterally to the olfactory bulbs. Previous claims of the absence of the vomero-nasal organs in archosaurs, which is suggested by the extant phylogenetic bracket, are questioned because its absence in both clades of extant archosaurs seems to be directly related with the independent acquisition of a non-ground living mode of life

    Cranial ontogenetic variation in early saurischians and the role of heterochrony in the diversification of predatory dinosaurs

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    Non-avian saurischian skulls underwent at least 165 million years of evolution and shapes varied from elongated skulls, such as in the theropod Coelophysis, to short and box-shaped skulls, such as in the sauropod Camarasaurus. A number of factors have long been considered to drive skull shape, including phylogeny, dietary preferences and functional constraints. However, heterochrony is increasingly being recognized as an important factor in dinosaur evolution. In order to quantitatively analyse the impact of heterochrony on saurischian skull shape, we analysed five ontogenetic trajectories using two-dimensional geometric morphometrics in a phylogenetic framework. This allowed for the comparative investigation of main ontogenetic shape changes and the evaluation of how heterochrony affected skull shape through both ontogenetic and phylogenetic trajectories. Using principal component analyses and multivariate regressions, it was possible to quantify different ontogenetic trajectories and evaluate them for evidence of heterochronic events allowing testing of previous hypotheses on cranial heterochrony in saurischians. We found that the skull shape of the hypothetical ancestor of Saurischia likely led to basal Sauropodomorpha through paedomorphosis, and to basal Theropoda mainly through peramorphosis. Paedomorphosis then led from Orionides to Avetheropoda, indicating that the paedomorphic trend found by previous authors in advanced coelurosaurs may extend back into the early evolution of Avetheropoda. Not only are changes in saurischian skull shape complex due to the large number of factors that affected it, but heterochrony itself is complex, with a number of possible reversals throughout non-avian saurischian evolution. In general, the sampling of complete ontogenetic trajectories including early juveniles is considerably lower than the sampling of single adult or subadult individuals, which is a major impediment to the study of heterochrony on non-avian dinosaurs. Thus, the current work represents an exploratory analysis. To better understand the cranial ontogeny and the impact of heterochrony on skull evolution in saurischians, the data set that we present here must be expanded and complemented with further sampling from future fossil discoveries, especially of juvenile individuals

    Reproductive Suicide: Similar Mechanisms of Aging in C. elegans and Pacific Salmon

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    In some species of salmon, reproductive maturity triggers the development of massive pathology resulting from reproductive effort, leading to rapid post-reproductive death. Such reproductive death, which occurs in many semelparous organisms (with a single bout of reproduction), can be prevented by blocking reproductive maturation, and this can increase lifespan dramatically. Reproductive death is often viewed as distinct from senescence in iteroparous organisms (with multiple bouts of reproduction) such as humans. Here we review the evidence that reproductive death occurs in C. elegans and discuss what this means for its use as a model organism to study aging. Inhibiting insulin/IGF-1 signaling and germline removal suppresses reproductive death and greatly extends lifespan in C. elegans, but can also extend lifespan to a small extent in iteroparous organisms. We argue that mechanisms of senescence operative in reproductive death exist in a less catastrophic form in iteroparous organisms, particularly those that involve costly resource reallocation, and exhibit endocrine-regulated plasticity. Thus, mechanisms of senescence in semelparous organisms (including plants) and iteroparous ones form an etiological continuum. Therefore understanding mechanisms of reproductive death in C. elegans can teach us about some mechanisms of senescence that are operative in iteroparous organisms

    Systematics and evolutionary history of proterosuchian archosauriforms

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    The evolutionary history of archosauromorphs is of particular interest because it includes the origins of two of the best-known and most distinctive extant tetrapod groups: crocodylians and birds. In this thesis, the anatomy, taxonomy and systematics of the Permo-Triassic non-archosaur archosauromorphs are revised. A revision of the Permo-Triassic archosauromorph record indicates that only four Permian species are known and there are three valid proterosuchid species immediately after the Permo-Triassic boundary in South Africa. Analyses of cranial ontogenetic variation in ProterosuchusProterosuchus fergusifergusi found that ontogenetic modification events (e.g. heterochrony) may have been key drivers of the evolution of the general shape of the skull at the base of Archosauriformes. A comprehensive quantitative phylogenetic analysis recovered a polyphyletic “Prolacertiformes”, restricted the taxonomic content of Proterosuchidae to only six species, Erythrosuchidae was composed of eight nominal species, and EuparkeriaEuparkeria capensiscapensis was found as the sister-taxon of the clade that includes proterochampsians (doswelliids + proterochampsids) and archosaurs. The results obtained here suggest that the evolutionary history of the archosauriforms during the Early Triassic can be subdivided into a first phase characterized by the short-lived “disaster-clade” Proterosuchidae and a second phase that witnessed the initial morphological and probably palaeoecological diversification of the group

    A revision of the ‘coelophysoid-grade’ theropod specimen from the Lower Jurassic of the Isle of Skye (Scotland)

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    The broadest diversification of early predatory dinosaurs is represented by the ‘coelophysoid-grade’ neotheropods, but their Hettangian–Sinemurian (c. 191–201 Ma) record is scarce worldwide. More information is needed to shed light on the evolution of this dinosaur group after the end-Triassic mass extinction (c. 201 Ma). Here we revisit the anatomy and phylogeny of one of these earliest Jurassic neotheropod specimens, an isolated partial tibia from the lower Sinemurian of the Isle of Skye (Scotland) that was previously identified as probably closely related to Liliensternus liliensterni and coelophysids. However, we found that the Skye specimen is positioned in the branch leading to Averostra (Ceratosauria + Tetanurae), in a polytomy with Sarcosaurus woodi from the late Hettangian–lower Sinemurian of central England and a clade composed of Tachiraptor admirabilis and Averostra. The morphology of the Skye specimen is congruent with that of referred specimens of Sarcosaurus woodi, but because it probably represents a skeletally immature specimen, we assign it to cf. Sarcosaurus woodi. The Skye specimen increases the number of averostran-line neotheropod specimens recorded in the Lower Jurassic of Europe and current evidence indicates that these forms, and not coelophysoids, were relatively common in this part of the world at that time

    Early dinosaur radiation: testing macroevolutionary models through diversification rate shift analyses of an early Mesozoic amniotan supertree

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    The early radiation of dinosaurs has been traditionally explained through a "competitive model", which attributes dinosaur success to their superiority in a drawn-out process involving inter-specific competition, or a more accepted "opportunistic model", which states that dinosaur radiation occurred in an empty ecospace cleared by two successive Late Triassic extinctions. Following the "opportunistic model", it would be expected that dinosaurs acquired diversification shifts only after the Late Triassic extinctions. Conversely, in the "competitive model" diversification shifts would be expected during the evanescence of their competitors. With the aim to test how these models fit to current phylogenetic reconstructions, a diversification rate analysis was performed on an amniotan supertree of 690 taxa. We found that the early dinosaur phylogeny significantly departs from a stochastic branching model (p<0.001) and a significant branching shift is located at the base of Dinosauria (p<0.05). This result is in agreement with the high diversity of early dinosaurs observed in the Ischigualasto Formation (early Late Triassic), clearly supporting that the dinosaur radiation started before the end-Ischigualastian extinction (middle Late Triassic). Ischigualastian continental assemblages were dominated by rhynchosaurs and traversodontids, and crurotarsans were common faunistic elements, indicating that the early radiation of dinosaurs firstly took place into a crowded-ecospace. However, branching patterns are not homogenous within Dinosauria: diversification shifts for Theropoda occurred at Ischigualastian and Hettangian-Sinemurian times (Early Jurassic), but in the case of Sauropodormorpha and Ornithischia the shifts took place in the Coloradian (latest Late Triassic), immediately after the end-Ischigualastian extinction. Together with herbivorous dinosaurs another six significant/conspicuous branching shifts are also recorded among Coloradian amniotan clades (e.g., mammaliamorphs, crocodylomorphs, pterosaurs), indicating that this stage of diversification was also experienced by another amniotan lineages. Accordingly, the early radiation of dinosaurs started during the Ischigualastian in a crowded-ecospace, showing different patterns within the group later in the Triassic, within a macroevolutionary scenario that does not completely fit with none of the two traditional models.Sesiones libresFacultad de Ciencias Naturales y Muse

    Early archosauromorph remains from the Permo-Triassic Buena Vista Formation of north-eastern Uruguay

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    The Permo-Triassic archosauromorph record is crucial to understand the impact of the Permo-Triassic mass extinction on the early evolution of the group and its subsequent dominance in Mesozoic terrestrial ecosystems. However, the Permo-Triassic archosauromorph record is still very poor in most continents and hampers the identification of global macroevolutionary patterns. Here we describe cranial and postcranial bones from the Permo-Triassic Buena Vista Formation of northeastern Uruguay that contribute to increase the meagre early archosauromorph record from South America. A basioccipital fused to both partial exoccipitals and three cervical vertebrae are assigned to Archosauromorpha based on apomorphies or a unique combination of characters. The archosauromorph remains of the Buena Vista Formation probably represent a multi-taxonomic assemblage composed of non-archosauriform archosauromorphs and a ‘proterosuchid-grade’ animal. This assemblage does not contribute in the discussion of a Late Permian or Early Triassic age for the Buena Vista Formation, but reinforces the broad palaeobiogeographic distribution of ‘proterosuchid grade’ diapsids in Permo-Triassic beds worldwide

    New clade of enigmatic early archosaurs yields insights into early pseudosuchian phylogeny and the biogeography of the archosaur radiation

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    BACKGROUND: The origin and early radiation of archosaurs and closely related taxa (Archosauriformes) during the Triassic was a critical event in the evolutionary history of tetrapods. This radiation led to the dinosaur-dominated ecosystems of the Jurassic and Cretaceous, and the high present-day archosaur diversity that includes around 10,000 bird and crocodylian species. The timing and dynamics of this evolutionary radiation are currently obscured by the poorly constrained phylogenetic positions of several key early archosauriform taxa, including several species from the Middle Triassic of Argentina (Gracilisuchus stipanicicorum) and China (Turfanosuchus dabanensis, Yonghesuchus sangbiensis). These species act as unstable ‘wildcards’ in morphological phylogenetic analyses, reducing phylogenetic resolution. RESULTS: We present new anatomical data for the type specimens of G. stipanicicorum, T. dabanensis, and Y. sangbiensis, and carry out a new morphological phylogenetic analysis of early archosaur relationships. Our results indicate that these three previously enigmatic taxa form a well-supported clade of Middle Triassic archosaurs that we refer to as Gracilisuchidae. Gracilisuchidae is placed basally within Suchia, among the pseudosuchian (crocodile-line) archosaurs. The approximately contemporaneous and morphologically similar G. stipanicicorum and Y. sangbiensis may be sister taxa within Gracilisuchidae. CONCLUSIONS: Our results provide increased resolution of the previously poorly constrained relationships of early archosaurs, with increased levels of phylogenetic support for several key early pseudosuchian clades. Moreover, they falsify previous hypotheses suggesting that T. dabanensis and Y. sangbiensis are not members of the archosaur crown group. The recognition of Gracilisuchidae provides further support for a rapid phylogenetic diversification of crown archosaurs by the Middle Triassic. The disjunct distribution of the gracilisuchid clade in China and Argentina demonstrates that early archosaurs were distributed over much or all of Pangaea although they may have initially been relatively rare members of faunal assemblages
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