74,438 research outputs found

    Utility of molecular phylogenetic methods: a critique of immuno-taxonomy

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    Immuno-taxonomy and the reconstruction of brachiopod phylogeny

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    In response to an earlier critique (Cohen 1992), immuno-taxonomy has been defended as providing a timely and practical approach to brachiopod systematics (Curry et al. 1993). Although the concept of applying this methodology to the brachiopod shell is novel and worthwhile, and has the potential importance for palaeobiology, the alternative analysis given here suggests that its practical utility remains highly uncertain because of conceptual and methodological limitations. These limitations cast doubt on, but do not necessarily disprove, systematic relationships inferred from the immuno-taxonomic data (Collins et al. 1991c; (Curry et al. 1991)

    Monophyly of brachiopods and phoronids: reconciliation of molecular evidence with Linnaean classification (the subphylum Phoroniformea nov.)

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    Molecular phylogenetic analyses of aligned 18S rDNA gene sequences from articulate and inarticulate brachiopods representing all major extant lineages, an enhanced set of phoronids and several unrelated protostome taxa, confirm previous indications that in such data, brachiopod and phoronids form a well-supported clade that (on previous evidence) is unambiguously affiliated with protostomes rather than deuterostomes. Within the brachiopod-phoronid clade, an association between phoronids and inarticulate brachiopods is moderately well supported, whilst a close relationship between phoronids and craniid inarticulates is weakly indicated. Brachiopod-phoronid monophyly is reconciled with the most recent Linnaean classification of brachiopods by abolition of the phylum Phoronida and rediagnosis of the phylum Brachiopoda to include tubiculous, shell-less forms. Recognition that brachiopods and phoronids are close genealogical allies of protostome phyla such as molluscs and annelids, but are much more distantly related to deuterostome phyla such as echinoderms and chordates, implies either (or both) that the morphology and ontogeny of blastopore, mesoderm and coelom formation have been widely misreported or misinterpreted, or that these characters have been subject to extensive homoplasy. This inference, if true, undermines virtually all morphology-based reconstructions of phylogeny made during the past century or more

    Control of dipolar relaxation in external fields

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    We study dipolar relaxation in both ultra-cold thermal and Bose-condensed chromium atom gases. We show three different ways to control dipolar relaxation, making use of either a static magnetic field, an oscillatory magnetic field, or an optical lattice to reduce the dimensionality of the gas from 3D to 2D. Although dipolar relaxation generally increases as a function of a static magnetic field intensity, we find a range of non-zero magnetic field intensities where dipolar relaxation is strongly reduced. We use this resonant reduction to accurately determine the S=6 scattering length of chromium atoms: a6=103±4a0a_6 = 103 \pm 4 a_0. We compare this new measurement to another new determination of a6a_6, which we perform by analysing the precise spectroscopy of a Feshbach resonance in d-wave collisions, yielding a6=102.5±0.4a0a_6 = 102.5 \pm 0.4 a_0. These two measurements provide by far the most precise determination of a6a_6 to date. We then show that, although dipolar interactions are long-range interactions, dipolar relaxation only involves the incoming partial wave l=0l=0 for large enough magnetic field intensities, which has interesting consequences on the stability of dipolar Fermi gases. We then study ultra-cold chromium gases in a 1D optical lattice resulting in a collection of independent 2D gases. We show that dipolar relaxation is modified when the atoms collide in reduced dimensionality at low magnetic field intensities, and that the corresponding dipolar relaxation rate parameter is reduced by a factor up to 7 compared to the 3D case. Finally, we study dipolar relaxation in presence of radio-frequency (rf) oscillating magnetic fields, and we show that both the output channel energy and the transition amplitude can be controlled by means of rf frequency and Rabi frequency.Comment: 25 pages, 17 figure

    Defining extreme sport: conceptions and misconceptions

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    One feature in how sport is defined is the distinction between extreme and non-extreme. BASE jumping is an example of an ‘extreme sport’ because it involves a high degree of ‘risk’, whilst swimming is classified as ‘non-extreme’ because the risks are minimal. This broad definition falls short of identifying the extent of risk and ignores the psychological, social-demographic and life style variables associated with engagement in each sport
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