21,023 research outputs found

    Orthonectids Are Highly Degenerate Annelid Worms

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    The animal groups of Orthonectida and Dicyemida are tiny, extremely simple, vermiform endoparasites of various marine animals and have been linked in the Mesozoa (Figure 1). The Orthonectida (Figures 1A and 1B) have a few hundred cells, including a nervous system of just ten cells, and the Dicyemida (Figure 1C) are even simpler, with āˆ¼40 cells. They are classic ā€œProblematicaā€ā€”the name Mesozoa suggests an evolutionary position intermediate between Protozoa and Metazoa (animals) and implies that their simplicity is a primitive state, but molecular data have shown they are members of Lophotrochozoa within Bilateria, which means that they derive from a more complex ancestor. Their precise affinities remain uncertain, however, and it is disputed whether they even constitute a clade. Ascertaining their affinities is complicated by the very fast evolution observed in their genes, potentially leading to the common systematic error of long-branch attraction (LBA). Here, we use mitochondrial and nuclear gene sequence data and show that both dicyemids and orthonectids are members of the Lophotrochozoa. Carefully addressing the effects of unequal rates of evolution, we show that the Mesozoa is polyphyletic. While the precise position of dicyemids remains unresolved within Lophotrochozoa, we identify orthonectids as members of the phylum Annelida. This result reveals one of the most extreme cases of body-plan simplification in the animal kingdom; our finding makes sense of an annelid-like cuticle in orthonectids and suggests that the circular muscle cells repeated along their body may be segmental in origin

    The electronic structure of Be and BeO: Benchmark EMS measurements and LCAO calculations

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    The electronic band structures of Be and BeO have been measured by transmission electron momentum spectroscopy (EMS). The low atomic number of beryllium and the use of ultrathin solid films in these experiments reduce the probability of electron multiple scattering within the sample, resulting in very clean 'benchmark' measurements for the EMS technique. Experimental data are compared to tight-binding (LCAO) electronic structure calculations using Hartree-Fock, and local density (LDA-VWN), gradient corrected (PBE) and hybrid (PBE0) density functional theory. Overall, DFT calculations reproduce the EMS data for metallic Be reasonably well. PBE predictions for the valence bandwidth of Be are in excellent agreement with EMS data, provided the calculations employ a large basis set augmented with diffuse functions. For BeO, PBE calculations using a moderately sized basis set are in reasonable agreement with experiment, slightly underestimating the valence bandgap and overestimating the O(2s) and O(2p) bandwidths. The calculations also underestimate the EMS intensity of the O(2p) band around the Ī“-point. Simulation of the effects of multiple scattering in the calculated oxide bandstructures do not explain these systematic differences. Crown Copyright Ā© 2002 Published by Elsevier Science Ltd. All rights reserved

    Nitrogen supplements effect on amylase production by Aspergillus niger using cassava whey medium

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    The production of amylase by Aspergillus niger on three cassava whey media in liquid shake culture was compared. The supplemented cassava whey (SCW) medium exhibited gave amylase activity of 495 U/ml. Biomass cropped was 1.63 g/l in the SCW medium. Yeast extract employed as a nitrogensupplement increased biomass yield of A. niger to 2.75 g/l with maximum amylase activity of 643 U/ml. Sodium nitrate (NaNO3) as nitrogen supplement had the lowest biomass yield of 0.77 g/l and amylase activity of 206 U/ml. Thus yeast extract as nitrogen supplement of cassava whey medium supported maximum production of amylase and biomass of A. niger

    The mitochondrial genomes of the acoelomorph worms Paratomella rubra, Isodiametra pulchra and Archaphanostoma ylvae

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    Acoels are small, ubiquitous - but understudied - marine worms with a very simple body plan. Their internal phylogeny is still not fully resolved, and the position of their proposed phylum Xenacoelomorpha remains debated. Here we describe mitochondrial genome sequences from the acoels Paratomella rubra and Isodiametra pulchra, and the complete mitochondrial genome of the acoel Archaphanostoma ylvae. The P. rubra and A. ylvae sequences are typical for metazoans in size and gene content. The larger I. pulchraĀ  mitochondrial genome contains both ribosomal genes, 21 tRNAs, but only 11 protein-coding genes. We find evidence suggesting a duplicated sequence in the I. pulchra mitochondrial genome. The P. rubra, I. pulchra and A. ylvae mitochondria have a unique genome organisation in comparison to other metazoan mitochondrial genomes. We found a large degree of protein-coding gene and tRNA overlap with little non-coding sequence in the compact P. rubra genome. Conversely, the A. ylvae and I. pulchra genomes have many long non-coding sequences between genes, likely driving genome size expansion in the latter. Phylogenetic trees inferred from mitochondrial genes retrieve Xenacoelomorpha as an early branching taxon in the deuterostomes. Sequence divergence analysis between P. rubra sampled in England and Spain indicates cryptic diversity

    Atomic and Molecular Interstellar Absorption Lines toward the High Galactic Latitude Stars HD 141569 and HD 157841 at Ultra-High Resolution

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    We present ultra-high-resolution (0.32 km s-1) spectra obtained with the 3.9 m Anglo-Australian Telescope (AAT) and Ultra-High-Resolution Facility (UHRF) of interstellar Na I D1, Na I D2, Ca II K, K I, and CH absorption toward two high Galactic latitude stars HD 141569 and HD 157841. We have compared our data with 21 cm observations obtained from the Leiden/Dwingeloo H I survey. We derive the velocity structure and column densities of the clouds represented by the various components and identify the clouds with ISM structures seen in the region at other wavelengths. We further derive abundances, linear depletions, and H2 fractional abundances for these clouds wherever possible. Both stars are located in regions of IRAS 100 Ī¼m emission associated with high Galactic latitude molecular clouds (HLCs): HD 141569 lies, in projection, close to MBM 37 and the Lynds dark cloud L134N, whereas HD 157841 is in the vicinity of the MBM 151. Toward HD 141569 we detect two components in our UHRF spectra: a weak, broad b = 4.5 km s-1 component at -15 km s-1, seen only in Ca II K absorption, and another component at 0 km s-1, seen in Na I D1, Na I D2, Ca II K, K I, and CH absorption. The cloud represented by the -15 km s-1 component is warm and may be located in a region close to the star. The cloud represented by the 0 km s-1 component has a Ca linear depletion Ī“(Ca) = 1.4 Ɨ 10-4 and shows evidence for the presence of dust, consistent with strong 100 Ī¼m emission seen in this region. The H2 fractional abundance f(H2) derived for this cloud is 0.4, which is typically what is observed toward HLCs. We conclude that this 0 km s-1 cloud is associated with MBM 37 and L134N based on the presence of dust and molecular gas (CH) and good velocity agreement with CO emission from these two clouds. This places HD 141569 beyond MBM 37 and L134N, which are estimated to be at ā‰ˆ 110 pc. In the case of the HD 157841 sight line, a total of six components are seen on our UHRF spectra in Na I D1, Na I D2, Ca II K, K I, and CH absorption. Two of these six components are seen only in a single species. The cloud represented by the components at 1.85 km s-1 has a Ca linear depletion Ī“(Ca) = 2.8 Ɨ 10-4, indicating the presence of dust. The f(H2) derived for this cloud is 0.45, and there is good velocity agreement with CO emission from MBM 151. To the best of our knowledge, this 1.85 km s-1 component toward HD 157841 is the first one found to have relative line widths that are consistent with pure thermal broadening only. We associate the 1.85 km s-1 cloud seen in our UHRF spectra with MBM 151 and conclude that HD 157841 must lie beyond ~200 pc, the estimated distance to MBM 151
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