810 research outputs found

    Halcyornis toliapicus (aves: Lower Eocene, England) indicates advanced neuromorphology in Mesozoic Neornithes

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    Our recent X-ray micro computer-tomographic (μCT) investigations of Prophaethon shrubsolei and Odontopteryx toliapica from the Lower Eocene London Clay Formation of England revealed the avian brain to have been essentially modern in form by 55 Ma, but that an important vision-related synapomorphy of living birds, the eminentia sagittalis of the telencephalon, was poorly developed. This evidence suggested that the feature probably appeared close to the end of the Mesozoic. Here we use μCT analysis to describe the endocranium of Halcyornis toliapicus, also from the London Clay Formation. The affinities of Halcyornis have been hotly debated, with the taxon referred to the Charadriiformes (Laridae), Coraciiformes (Alcedinidae, and its own family Halcyornithidae) and most recently that Halcyornithidae may be a possible senior synonym of Pseudasturidae (Pan-Psittaciformes). Unlike Prophaethon and Odontopteryx, the eminentia sagittalis of Halcyornis is strongly developed and comparable to that of living species. Like those London Clay taxa, the eminentia sagittalis occupies a rostral position on the telencephalon. The senses of Halcyornis appear to have been well developed. The length of the cochlear duct of the inner ear indicates a hearing sensitivity within the upper range of living species, and enlarged olfactory lobes suggest a reasonable reliance on sense of smell. The optic nerves were especially well developed which, together with the strong development of the eminentia sagittalis, indicates a high degree of visual specialization in Halcyornis. The advanced development of the eminentia sagittalis further supports a Mesozoic age for the appearance of this structure and associated neural architectural complexity found in extant Aves. The eminentia sagittalis of living Psittaciformes is situated caudally on the telencephalon, making a Pan-Psittaciformes relationship unlikely for Halcyorni

    The braincase and inner ear of ‘Metriorhynchus’ cf. ‘M.’ brachyrhynchus – implications for aquatic sensory adaptations in crocodylomorphs

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    During their long evolutionary history crocodylomorphs achieved a great diversity of body sizes, ecomorphotypes and inferred feeding ecologies. One unique group of crocodylomorphs are the thalattosuchians, which lived during the Jurassic and Cretaceous (ca. 191–125 Ma). They transitioned from shallow marine species, like teleosauroids, into fully pelagic forms with paddle shaped limbs and a vertically orientated tail fluke, the metriorhynchids. The osteological adaptations that allowed metriorhynchids to live in the water are generally well understood, but less is known about their neurosensory and endocranial systems, such as the brain, inner ears, sinuses and cranial nerves and how they relate to their aquatic lifestyle. Based on micro-computed tomography (μCT) data and three-dimensional models, we here describe the braincase and endocranial anatomy of a fully marine metriorhynchid, ‘Metriorhynchus’ cf. ‘M.’ brachyrhynchus (NHMUK PV OR 32617). We found several neuroanatomical features that likely helped this species function in its marine environment. These include a unique flexure in the brain endocast not seen in other thalattosuchians. Other features that have previously been seen in thalattosuchians include enlarged cerebral hemispheres, a hypertrophied venous sinus system, enlarged internal carotid arteries and foramina, and closed/absent lateral pharyngotympanic foramina. The specimen also possesses a pelagic metriorhynchid bony labyrinth morphology, with a compact and dorsoventrally short shape, thick semicircular canals, an enlarged vestibule and potentially a short cochlear duct. A review of character distribution confirms that some of these features evolved at the base of Thalattosuchia in semiaquatic species, long before metriorhynchids became pelagic, suggesting that endocranial anatomy helped allow metriorhynchoids colonize the ocean realm.Fil: Schwab, Julia A.. University of Edinburgh; Reino UnidoFil: Young, Mark T.. University of Edinburgh; Reino UnidoFil: Herrera, Laura Yanina. Universidad Nacional de La Plata. Facultad de Ciencias Naturales y Museo. División Paleontología Vertebrados; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata; ArgentinaFil: Witmer, Lawrence. Ohio University; Estados UnidosFil: Walsh, Stig A.. University of Southampton; Reino UnidoFil: Katsamensis, Orestis. Faculty Of Engineering And Physical Sciences; Reino UnidoFil: Brusatte, Stephen L.. University of Edinburgh; Reino Unid

    A method for mapping morphological convergence on three-dimensional digital models: the case of the mammalian sabre-tooth

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    Morphological convergence can be assessed using a variety of statistical methods. None of the methods proposed to date enable the visualization of convergence. All are based on the assumption that the phenotypes either converge, or do not. However, between species, morphologically similar regions of a larger structure may behave differently. Previous approaches do not identify these regions within the larger structures or quantify the degree to which they may contribute to overall convergence. Here, we introduce a new method to chart patterns of convergence on three-dimensional models using the R function conv.map. The convergence between pairs of models is mapped onto them to visualize and quantify the morphological convergence. We applied conv.map to a well-known case study, the sabre-tooth morphotype, which has evolved independently among distinct mammalian clades from placentals to metatherians. Although previous authors have concluded that sabre-tooths kill using a stabbing ‘bite’ to the neck, others have presented different interpretations for specific taxa, including the iconic Smilodon and Thylacosmilus. Our objective was to identify any shared morphological features among the sabre-tooths that may underpin similar killing behaviours. From a sample of 49 placental and metatherian carnivores, we found stronger convergence among sabre-tooths than for any other taxa. The morphological convergence is most apparent in the rostral and posterior parts of the cranium. The extent of this convergence suggests similarity in function among these phylogenetically distant species. In our view, this function is most likely to be the killing of relatively large prey using a stabbing bite. © 2021 The Authors. Palaeontology published by John Wiley & Sons Ltd on behalf of The Palaeontological Association

    ‘Ear stones’ in crocodylians: a cross-species comparative and ontogenetic survey of otolith structures

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    The vestibular system of the inner ear is a crucial sensory organ, involved in the sensation of balance and equilibrium. It consists of three semicircular canals that sense angular rotations of the head and the vestibule that detects linear acceleration and gravity. The vestibule often contains structures, known as the otoliths or ‘ear stones’. Otoliths are present in many vertebrates and are particularly well known from the fossil record of fish, but surprisingly have not been described in detail in most tetrapods, living or extinct. Here, we present for the first time a survey of the otoliths of a broad sample of extant crocodylian species, based on computed tomography scans. We find that otoliths are present in numerous crocodylian species of different growth stages, and they continue to increase in size during ontogeny, with positive allometry compared to skull length. Our results confirm that otoliths are a common component of the crocodylian vestibular system, and suggest they play an important role in sensory detection. Otoliths are likely common, but overlooked, constituents of the inner ear in tetrapods, and a broader study of their size, shape and distribution promises insight into sensory abilities

    Evolutionary integration and modularity in the archosaur cranium

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    Complex structures, like the vertebrate skull, are composed of numerous elements or traits that must develop and evolve in a coordinated manner to achieve multiple functions. The strength of association among phenotypic traits (i.e., integration), and their organization into highly-correlated, semi-independent subunits termed modules, is a result of the pleiotropic and genetic correlations that generate traits. As such, patterns of integration and modularity are thought to be key factors constraining or facilitating the evolution of phenotypic disparity by influencing the patterns of variation upon which selection can act. It is often hypothesized that selection can reshape patterns of integration, parceling single structures into multiple modules or merging ancestrally semi-independent traits into a strongly correlated unit. However, evolutionary shifts in patterns of trait integration are seldom assessed in a unified quantitative framework. Here, we quantify patterns of evolutionary integration among regions of the archosaur skull to investigate whether patterns of cranial integration are conserved or variable across this diverse group. Using high-dimensional geometric morphometric data from 3D surface scans and CT scans of modern birds (n = 352), fossil non-avian dinosaurs (n = 27), and modern and fossil mesoeucrocodylians (n = 38), we demonstrate that some aspects of cranial integration are conserved across these taxonomic groups, despite their major differences in cranial form, function, and development. All three groups are highly modular and consistently exhibit high integration within the occipital region. However, there are also substantial divergences in correlation patterns. Birds uniquely exhibit high correlation between the pterygoid and quadrate, components of the cranial kinesis apparatus, whereas the non-avian dinosaur quadrate is more closely associated with the jugal and quadratojugal. Mesoeucrocodylians exhibit a slightly more integrated facial skeleton overall than the other grades. Overall, patterns of trait integration are shown to be stable among archosaurs, which is surprising given the cranial diversity exhibited by the clade. At the same time, evolutionary innovations such as cranial kinesis that reorganize the structure and function of complex traits can result in modifications of trait correlations and modularity

    A prospective study of von Willebrand factor levels and bleeding in pregnant women with type 1 von Willebrand disease

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/134934/1/hae13086.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/134934/2/hae13086_am.pd

    Relationship between latent and rebound viruses in a clinical trial of anti-HIV-1 antibody 3BNC117.

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    A clinical trial was performed to evaluate 3BNC117, a potent anti-HIV-1 antibody, in infected individuals during suppressive antiretroviral therapy and subsequent analytical treatment interruption (ATI). The circulating reservoir was evaluated by quantitative and qualitative viral outgrowth assay (Q2VOA) at entry and after 6 mo. There were no significant quantitative changes in the size of the reservoir before ATI, and the composition of circulating reservoir clones varied in a manner that did not correlate with 3BNC117 sensitivity. 3BNC117 binding site amino acid variants found in rebound viruses preexisted in the latent reservoir. However, only 3 of 217 rebound viruses were identical to 868 latent viruses isolated by Q2VOA and near full-length sequencing. Instead, 63% of the rebound viruses appeared to be recombinants, even in individuals with 3BNC117-resistant reservoir viruses. In conclusion, viruses emerging during ATI in individuals treated with 3BNC117 are not the dominant species found in the circulating latent reservoir, but frequently appear to represent recombinants of latent viruses

    Chapter sixteen: Rodents and other vertebrate invaders in the United States

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    Contents 16.1 Introduction 381 16.2 Assessing impacts of rodents and other vertebrate invaders 385 16.3 Accounts of some important vertebrate invaders 38616.3.1 Norway rant (Rattus norvegicus) 38616.3.2 Roof Rat (Rattus rattus) 38716.3.3 Polynesian rat (Rattus exulans) 38816.3.4 House mouse (Mus Musculus) 38816.3.5 Nutria (Myocastor coypus) 38916.3.6 Gambian giant pouched rat (Cricetomys gambianus) 39016.3.7 Feral swine (Sus scofa) 39016.3.8 Small Indian Mongoose (Herpestes javanicus) 39116.3.9 Rock pigeon (Columba livia) 39216.3.10 House sparrow (Passer domesticus) 39316.3.11 European starling (Sturnus vulgaris) 39316.3.12 Monk parakeet (Myiopsitta monachus) 39416.3.13 Brown tree snake (Boiga irregularis) 39516.3.14 Burmese python (Python molurus bivittatus) 39616.3.15 Coqui frog (Eleutherodactylus coqui) 39716.3.16 Sea lamprey (Petromyzon marinus) 39716.3.17 European and Asian carp (Cyprinidae) 398 16.4 Offshore Threats 399 16.5 Discussion 400 Acknowledgements 401 References 40
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