150 research outputs found

    The fossil record of the family Benthopectinidae (Echinodermata, Asteroidea), a reappraisal

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    Fossils assigned to the predominantly deep-sea asteroid family Benthopectinidae Verrill, 1894 are described and their affinities reappraised. Detailed comparative morphology of ambulacrals, adambulacrals and marginal ossicles has revealed that only some extinct taxa fall within the morphological range of the modern representatives of the family. These include Jurapecten hessi Gale, 2011, J. infrajurensis sp. nov. (both Jurassic), J. dhondtae sp. nov. (Upper Cretaceous) and Nearchaster spinosus (Blake, 1973) comb. nov. (Lower Oligocene). A new Late Cretaceous genus, Punkaster gen. nov. (P. spinifera gen. et sp. nov. and P. ruegenensis gen. et sp. nov.), appears to be a highly derived benthopectinid. A possible benthopectinid is described from the Upper Triassic (Carnian) of China. Other described records are distantly related to, but convergent in gross morphology with, benthopectinids. Thus, Plesiastropecten hallovensis Peyer, 1944 is here referred to the Jurassic spinulosidan family Plumasteridae Gale, 2011 and Xandarosaster hessi Blake, 1984 is interpreted as Spinulosida Perrier, 1884 incertae sedis. The mid-Cretaceous Alkaidia sumralli Blake & Reid, 1998 is reassigned to the Forcipulatida (Zorocallina). The “fossil benthopectinid” of Spencer & Wright in Moore (1966) is shown to belong to the goniopectinid genus Chrispaulia Gale, 2005, of which two new Cretaceous species are described, C. wrightorum sp. nov. and C. spinosa sp. nov. Finally, we consider Henricia? venturana Durham & Roberts, 1948 to be an indeterminate asteroid

    Mesozoic-Cenozoic crustaceans preserved within echinoid tests and bivalve shells

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    Associations of crustaceans with echinoids (Echinodermata) and bivalves (Mollusca) are not uncommon in modern oceans. Here we record the occurrence of anomurans, brachyurans and isopods within echinoid tests and bivalve shells from the Middle Jurassic of France, the Upper Jurassic of the Czech Republic, the Eocene of Croatia and the Miocene of Austria. Additionally a new genus and species of fossil cirolanid isopod from the Middle Jurassic of France is described. The present examples are interpreted as crustacean sheltering, probably for safe and undisturbed moulting (ecdysis), within a vacant host test or shell. However, accidental association (washed in) or even food remains cannot be ruled out entirelyWeb of Science90361160

    Three-dimensional dental microwear in type-Maastrichtian mosasaur teeth (Reptilia, Squamata)

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    Mosasaurs (Squamata, Mosasauridae) were large aquatic reptiles from the Late Cretaceous that filled a range of ecological niches within marine ecosystems. The type-Maastrichtian strata (68–66 Ma) of the Netherlands and Belgium preserve remains of five species that seemed to have performed different ecological roles (carnivores, piscivores, durophages). However, many interpretations of mosasaur diet and niche partitioning are based on qualitative types of evidence that are difficult to test explicitly. Here, we apply three-dimensional dental microwear texture analysis (DMTA) to provide quantitative dietary constraints for type-Maastrichtian mosasaurs, and to assess levels of niche partitioning between taxa. DMTA indicates that these mosasaurs did not exhibit neatly defined diets or strict dietary partitioning. Instead, we identify three broad groups: (i) mosasaurs Carinodens belgicus and Plioplatecarpus marshi plotting in the space of modern reptiles that are predominantly piscivorous and/or consume harder invertebrate prey, (ii) Prognathodon saturator and Prognathodon sectorius overlapping with extant reptiles that consume larger amounts of softer invertebrate prey items, and (iii) Mosasaurus hoffmanni spanning a larger plot area in terms of dietary constraints. The clear divide between the aforementioned first two groups in texture-dietary space indicates that, despite our small sample sizes, this method shows the potential of DMTA to test hypotheses and provide quantitative constraints on mosasaur diets and ecological roles

    Origin, early evolution and palaeoecology of Gymnopleura (Crustacea, Decapoda): Basal palaeocorystoid crabs from the Upper Jurassic-Lower Cretaceous of central Europe

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    Recent fieldwork has yielded new decapod crustacean material from Upper Jurassic-lowest Cretaceous bioclastic limestones at Kotou.c quarry near.Stramberk (Moravia, northeastern Czech Republic). Two specimens in this lot can be ascribed to the superfamily Palaeocorystoidea and represent the oldest gymnopleuran crabs known to date. A new genus and species, Moravacarcinus stramberkensis, are here erected and assigned to a new subfamily, Moravacarcininae, to accommodate this basal necrocarcinid. Our re-examination of Late Jurassic primitive crabs from southern Germany has resulted in the discovery of another early member of this group, here referred to a new genus, Juranecrocarcinus, as J. angulosum (Wehner, 1988). These new finds demonstrate that palaeocorystoids originated within shallow-water, reefal settings in the Upper Jurassic reef belt across central and southern Europe. We hypothesise that members of basal necrocarcinid subfamilies (Paranecrocarcininae and Moravacarcininae subfam. nov.), and thus the Gymnopleura, were derived from a dynomeniform ancestor which adapted to and became modified for a burying mode of life. Possible candidates are, for instance, the goniodromitid genus Cycloprosopon L.orenthey, in L.orenthey and Beurlen, 1929 and the longodromitid genera Longodromites Patrulius, 1959 and Planoprosopon Schweitzer, Feldmann and Laz.ar, 2007. The evolutionary pathways and palaeogeographical history of Mesozoic gymnopleurans were markedly influenced by the planktonic revolution which considerably enriched deeper-marine clastic sediments with nutrients from the Late Jurassic onwards.Web of Science564art. no. 11017

    Pharmacogenomic response of low dose haloperidol in critically ill adults with delirium

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    Purpose: To characterize the pharmacogenomic response of low-dose haloperidol for delirium treatment in critically ill adults. Materials and methods: Single-center, pilot study of a convenience sample of ICU adults with delirium treated with low-dose IV haloperidol. Patients were evaluated for delirium with the ICDSC every 8 h. Serum haloperidol concentrations were collected on ICU days 2–6, CYP2D6 and CYP3A4 genotypes were characterized and patients were categorized as extensive (EM), intermediate (IM) or poor metabolizers (PM). Results: The 22 patients (median age 67 [IQR 48,77] years; median APACHE III 81[IQR 54,181]; CYP2D6 [EM = 12, IM = 7, PM = 3], CYP3A [EM = 18, IM = 4]) received a median [IQR] daily haloperidol dose of 3.0 [2.4, 4.5] mg. After adjusting for age, SOFA, and ICU day, neither an association between CYP2D6 (IM p = .67/PM p = .25) or CYP3A4 (IM p = .44) metabolizer status and serum haloperidol concentrations was found. After adjusting for age, SOFA, and ICU day, neither an association between daily haloperidol dose (p = .77) or ICDSC score (p = .13) and serum haloperidol concentrations was found. No patient experienced QTc interval prolongation (≥500 ms). Conclusions: This pilot study, the first to evaluate the pharmacogenomic response of low-dose haloperidol when used to treat delirium in the ICU, suggests CYP2D6/CYP3A4 metabolizer status does not affect the serum haloperidol concentrations

    Comment on the letter of the Society of Vertebrate Paleontology (SVP) dated April 21, 2020 regarding 'Fossils from conflict zones and reproducibility of fossil‑based scientific data': Myanmar amber

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    Recently, the Society of Vertebrate Paleontology (SVP) has sent around a letter, dated 21st April, 2020 to more than 300 palaeontological journals, signed by the President, Vice President and a former President of the society (Rayfield et al. 2020). The signatories of this letter request significant changes to the common practices in palaeontology. With our present, multi-authored comment, we aim to argue why these suggestions will not lead to improvement of both practice and ethics of palaeontological research but, conversely, hamper its further development. Although we disagree with most contents of the SVP letter, we appreciate this initiative to discuss scientific practices and the underlying ethics. Here, we consider different aspects of the suggestions by Rayfield et al. (2020) in which we see weaknesses and dangers. It is our intent to compile views from many different fields of palaeontology, as our discipline is (and should remain) pluralistic. This contribution deals with the aspects concerning Myanmar amber. Reference is made to Haug et al. (2020a) for another comment on aspects concerning amateur palaeontologists/citizen scientists/private collectors

    Meta-analysis of genome-wide association studies for cattle stature identifies common genes that regulate body size in mammals

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    peer-reviewedH.D.D., A.J.C., P.J.B. and B.J.H. would like to acknowledge the Dairy Futures Cooperative Research Centre for funding. H.P. and R.F. acknowledge funding from the German Federal Ministry of Education and Research (BMBF) within the AgroClustEr ‘Synbreed—Synergistic Plant and Animal Breeding’ (grant 0315527B). H.P., R.F., R.E. and K.-U.G. acknowledge the Arbeitsgemeinschaft Süddeutscher Rinderzüchter, the Arbeitsgemeinschaft Österreichischer Fleckviehzüchter and ZuchtData EDV Dienstleistungen for providing genotype data. A. Bagnato acknowledges the European Union (EU) Collaborative Project LowInputBreeds (grant agreement 222623) for providing Brown Swiss genotypes. Braunvieh Schweiz is acknowledged for providing Brown Swiss phenotypes. H.P. and R.F. acknowledge the German Holstein Association (DHV) and the Confederación de Asociaciones de Frisona Española (CONCAFE) for sharing genotype data. H.P. was financially supported by a postdoctoral fellowship from the Deutsche Forschungsgemeinschaft (DFG) (grant PA 2789/1-1). D.B. and D.C.P. acknowledge funding from the Research Stimulus Fund (11/S/112) and Science Foundation Ireland (14/IA/2576). M.S. and F.S.S. acknowledge the Canadian Dairy Network (CDN) for providing the Holstein genotypes. P.S. acknowledges funding from the Genome Canada project entitled ‘Whole Genome Selection through Genome Wide Imputation in Beef Cattle’ and acknowledges WestGrid and Compute/Calcul Canada for providing computing resources. J.F.T. was supported by the National Institute of Food and Agriculture, US Department of Agriculture, under awards 2013-68004-20364 and 2015-67015-23183. A. Bagnato, F.P., M.D. and J.W. acknowledge EU Collaborative Project Quantomics (grant 516 agreement 222664) for providing Brown Swiss and Finnish Ayrshire sequences and genotypes. A.C.B. and R.F.V. acknowledge funding from the public–private partnership ‘Breed4Food’ (code BO-22.04-011- 001-ASG-LR) and EU FP7 IRSES SEQSEL (grant 317697). A.C.B. and R.F.V. acknowledge CRV (Arnhem, the Netherlands) for providing data on Dutch and New Zealand Holstein and Jersey bulls.Stature is affected by many polymorphisms of small effect in humans1. In contrast, variation in dogs, even within breeds, has been suggested to be largely due to variants in a small number of genes2,3. Here we use data from cattle to compare the genetic architecture of stature to those in humans and dogs. We conducted a meta-analysis for stature using 58,265 cattle from 17 populations with 25.4 million imputed whole-genome sequence variants. Results showed that the genetic architecture of stature in cattle is similar to that in humans, as the lead variants in 163 significantly associated genomic regions (P < 5 × 10−8) explained at most 13.8% of the phenotypic variance. Most of these variants were noncoding, including variants that were also expression quantitative trait loci (eQTLs) and in ChIP–seq peaks. There was significant overlap in loci for stature with humans and dogs, suggesting that a set of common genes regulates body size in mammals
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