114 research outputs found

    Hard and soft anatomy in two genera of Dondersiidae (Mollusca, Aplacophora, Solenogastres)

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    Author Posting. © Marine Biological Laboratory, 2012. This article is posted here by permission of Marine Biological Laboratory for personal use, not for redistribution. The definitive version was published in Biological Bulletin 222 (2012): 233-269.Phylogenetic relationships and identifications in the aplacophoran taxon Solenogastres (Neomeniomorpha) are in flux largely because descriptions of hard parts––sclerites, radulae, copulatory spicules––and body shape have often not been adequately illustrated or utilized. With easily recognizable and accessible hard parts, descriptions of Solenogastres are of greater use, not just to solenogaster taxonomists, but also to ecologists, paleontologists, and evolutionary biologists. Phylogenetic studies of Aplacophora, Mollusca, and the Lophotrochozoa as a whole, whether morphological or molecular, would be enhanced. As an example, morphologic characters, both isolated hard parts and internal anatomy, are provided for two genera in the Dondersiidae. Five species are described or redescribed and earlier descriptions corrected and enhanced. Three belong to Dondersia: D. festiva Hubrecht, D. incali (Scheltema), and D. namibiensis n. sp., the latter differentiated unambiguously from D. incali only by sclerites and copulatory spicules. Two species belong to Lyratoherpia: L. carinata Salvini-Plawen and L. californica (Heath). Notes are given for other species in Dondersiidae: L. bracteata Salvini-Plawen, Ichthyomenia ichthyodes (Pruvot), and Heathia porosa (Heath). D. indica Stork is synonymized with D. annulata. A cladistic morphological analysis was conducted to examine the utility of hard parts for reconstructing solenogaster phylogeny. Results indicate monophyly of Dondersia and Lyratoherpia as described here.Major funding was by a U. S. National Science Foundation grant (DEB-9521930) under the PEET program (Partnerships for Enhancing Expertise in Taxonomy)

    Phylogenomics of Aplacophora (Mollusca, Aculifera) and a solenogaster without a foot

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    Recent molecular phylogenetic investigations strongly supported the placement of the shell-less, worm-shaped aplacophoran molluscs (Solenogastres and Caudofoveata) and chitons (Polyplacophora) in a clade called Aculifera, which is the sister taxon of all other molluscs. Thus, understanding the evolutionary history of aculiferan molluscs is important for understanding early molluscan evolution. In particular, fundamental questions about evolutionary relationships within Aplacophora have long been unanswered. Here, we supplemented the paucity of available data with transcriptomes from 25 aculiferans and conducted phylogenomic analyses on datasets with up to 525 genes and 75 914 amino acid positions. Our results indicate that aplacophoran taxonomy requires revision as several traditionally recognized groups are non-monophyletic. Most notably, Cavibelonia, the solenogaster taxon defined by hollow sclerites, is polyphyletic, suggesting parallel evolution of hollow sclerites in multiple lineages. Moreover, we describe Apodomenia enigmatica sp. nov., a bizarre new species that appears to be a morphological intermediate between Solenogastres and Caudofoveata. This animal is not a missing link, however; molecular and morphological studies show that it is a derived solenogaster that lacks a foot, mantle cavity and radula. Taken together, these results shed light on the evolutionary history of Aplacophora and reveal a surprising degree of morphological plasticity within the group.publishedVersio

    New data from Monoplacophora and a carefully-curated dataset resolve molluscan relationships

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    Relationships among the major lineages of Mollusca have long been debated. Morphological studies have considered the rarely collected Monoplacophora (Tryblidia) to have several plesiomorphic molluscan traits. The phylogenetic position of this group is contentious as morphologists have generally placed this clade as the sister taxon of the rest of Conchifera whereas earlier molecular studies supported a clade of Monoplacophora +Polyplacophora (Serialia) and phylogenomic studies have generally recovered a clade of Monoplacophora +Cephalopoda. Phylogenomic studies have also strongly supported a clade including Gastropoda, Bivalvia, and Scaphopoda, but relationships among these taxa have been inconsistent. In order to resolve conchiferan relationships and improve understanding of early molluscan evolution, we carefully curated a high-quality data matrix and conducted phylogenomic analyses with broad taxon sampling including newly sequenced genomic data from the monoplacophoran Laevipilina antarctica. Whereas a partitioned maximum likelihood (ML) analysis using site-homogeneous models recovered Monoplacophora sister to Cephalopoda with moderate support, both ML and Bayesian inference (BI) analyses using mixture models recovered Monoplacophora sister to all other conchiferans with strong support. A supertree approach also recovered Monoplacophora as the sister taxon of a clade composed of the rest of Conchifera. Gastropoda was recovered as the sister taxon of Scaphopoda in most analyses, which was strongly supported when mixture models were used. A molecular clock based on our BI topology dates diversification of Mollusca to similar to 546 MYA (+/- 6 MYA) and Conchifera to similar to 540 MYA (+/- 9 MYA), generally consistent with previous work employing nuclear housekeeping genes. These results provide important resolution of conchiferan mollusc phylogeny and offer new insights into ancestral character states of major mollusc clades

    Intervento alla tavola rotonda "Dove sta andando la critica letteraria?"

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    Marginalità rispetto alle altre letterature e alle altre forme di comunicazione. È questa, secondo lo studioso, la condizione attuale della letteratura italiana nel sistema globalizzato. È necessario che l'interprete riscopra la sua triplice funzione - critico, filologo, storico della letteratura - per tentare di penetrare nel testo, anche grazie agli apporti fecondi della critica tematica e ai nuovi approcci interdisciplinari della comparatistica

    Assessment of mitochondrial genomes for heterobranch gastropod phylogenetics

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    Background Heterobranchia is a diverse clade of marine, freshwater, and terrestrial gastropod molluscs. It includes such disparate taxa as nudibranchs, sea hares, bubble snails, pulmonate land snails and slugs, and a number of (mostly small-bodied) poorly known snails and slugs collectively referred to as the “lower heterobranchs”. Evolutionary relationships within Heterobranchia have been challenging to resolve and the group has been subject to frequent and significant taxonomic revision. Mitochondrial (mt) genomes can be a useful molecular marker for phylogenetics but, to date, sequences have been available for only a relatively small subset of Heterobranchia. Results To assess the utility of mitochondrial genomes for resolving evolutionary relationships within this clade, eleven new mt genomes were sequenced including representatives of several groups of “lower heterobranchs”. Maximum likelihood analyses of concatenated matrices of the thirteen protein coding genes found weak support for most higher-level relationships even after several taxa with extremely high rates of evolution were excluded. Bayesian inference with the CAT + GTR model resulted in a reconstruction that is much more consistent with the current understanding of heterobranch phylogeny. Notably, this analysis recovered Valvatoidea and Orbitestelloidea in a polytomy with a clade including all other heterobranchs, highlighting these taxa as important to understanding early heterobranch evolution. Also, dramatic gene rearrangements were detected within and between multiple clades. However, a single gene order is conserved across the majority of heterobranch clades. Conclusions Analysis of mitochondrial genomes in a Bayesian framework with the site heterogeneous CAT + GTR model resulted in a topology largely consistent with the current understanding of heterobranch phylogeny. However, mitochondrial genomes appear to be too variable to serve as good phylogenetic markers for robustly resolving a number of deeper splits within this clade.publishedVersio

    Pluripotency and the origin of animal multicellularity

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    Funding: This study was supported by funds from the Australian Research Council (B.M.D. and S.M.D.).A widely held—but rarely tested—hypothesis for the origin of animals is that they evolved from a unicellular ancestor, with an apical cilium surrounded by a microvillar collar, that structurally resembled modern sponge choanocytes and choanoflagellates1,2,3,4. Here we test this view of animal origins by comparing the transcriptomes, fates and behaviours of the three primary sponge cell types—choanocytes, pluripotent mesenchymal archaeocytes and epithelial pinacocytes—with choanoflagellates and other unicellular holozoans. Unexpectedly, we find that the transcriptome of sponge choanocytes is the least similar to the transcriptomes of choanoflagellates and is significantly enriched in genes unique to either animals or sponges alone. By contrast, pluripotent archaeocytes upregulate genes that control cell proliferation and gene expression, as in other metazoan stem cells and in the proliferating stages of two unicellular holozoans, including a colonial choanoflagellate. Choanocytes in the sponge Amphimedon queenslandica exist in a transient metastable state and readily transdifferentiate into archaeocytes, which can differentiate into a range of other cell types. These sponge cell-type conversions are similar to the temporal cell-state changes that occur in unicellular holozoans5. Together, these analyses argue against homology of sponge choanocytes and choanoflagellates, and the view that the first multicellular animals were simple balls of cells with limited capacity to differentiate. Instead, our results are consistent with the first animal cell being able to transition between multiple states in a manner similar to modern transdifferentiating and stem cells.PostprintPeer reviewe
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