Literature DB >> 19274743

Myoanatomy of the marine tardigrade Halobiotus crispae (Eutardigrada: Hypsibiidae).

Kenneth Agerlin Halberg1, Dennis Persson, Nadja Møbjerg, Andreas Wanninger, Reinhardt Møbjerg Kristensen.   

Abstract

The muscular architecture of Halobiotus crispae (Eutardigrada: Hypsibiidae) was examined by means of fluorescent-coupled phalloidin in combination with confocal laser scanning microscopy and computer-aided three-dimensional reconstruction, in addition to light microscopy (Nomarski), scanning electron microscopy, and transmission electron microscopy (TEM). The somatic musculature of H. crispae is composed of structurally independent muscle fibers, which can be divided into a dorsal, ventral, dorsoventral, and a lateral musculature. Moreover, a distinct leg musculature is found. The number and arrangement of muscles differ in each leg. Noticeably, the fourth leg contains much fewer muscles when compared with the other legs. Buccopharyngeal musculature (myoepithelial muscles), intestinal musculature, and cloacal musculature comprise the animal's visceral musculature. TEM of stylet and leg musculature revealed ultrastructural similarities between these two muscle groups. Furthermore, microtubules are found in the epidermal cells of both leg and stylet muscle attachments. This would indicate that the stylet and stylet glands are homologues to the claw and claw glands, respectively. When comparing with previously published data on both heterotardigrade and eutardigrade species, it becomes obvious that eutardigrades possess very similar numbers and arrangement of muscles, yet differ in a number of significant details of their myoanatomy. This study establishes a morphological framework for the use of muscular architecture in elucidating tardigrade phylogeny. (c) 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19274743     DOI: 10.1002/jmor.10734

Source DB:  PubMed          Journal:  J Morphol        ISSN: 0022-2887            Impact factor:   1.804


  8 in total

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2.  The velvet worm brain unveils homologies and evolutionary novelties across panarthropods.

Authors:  Christine Martin; Henry Jahn; Mercedes Klein; Jörg U Hammel; Paul A Stevenson; Uwe Homberg; Georg Mayer
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3.  Distal oviduct and genital chamber of eriophyoids (Acariformes, Eriophyoidea): refined terminology and remarks on CLSM technique for studying musculature of mites.

Authors:  Philipp E Chetverikov
Journal:  Exp Appl Acarol       Date:  2014-07-23       Impact factor: 2.132

4.  Cambrian lobopodians and extant onychophorans provide new insights into early cephalization in Panarthropoda.

Authors:  Qiang Ou; Degan Shu; Georg Mayer
Journal:  Nat Commun       Date:  2012       Impact factor: 14.919

5.  Tracing the evolutionary origins of insect renal function.

Authors:  Kenneth A Halberg; Selim Terhzaz; Pablo Cabrero; Shireen A Davies; Julian A T Dow
Journal:  Nat Commun       Date:  2015-04-21       Impact factor: 14.919

6.  Desiccation tolerance in the tardigrade Richtersius coronifer relies on muscle mediated structural reorganization.

Authors:  Kenneth Agerlin Halberg; Aslak Jørgensen; Nadja Møbjerg
Journal:  PLoS One       Date:  2013-12-31       Impact factor: 3.240

7.  Comparative myoanatomy of Tardigrada: new insights from the heterotardigrades Actinarctus doryphorus (Tanarctidae) and Echiniscoides sigismundi (Echiniscoididae).

Authors:  Dennis Krog Persson; Kenneth Agerlin Halberg; Ricardo Cardoso Neves; Aslak Jørgensen; Reinhardt Møbjerg Kristensen; Nadja Møbjerg
Journal:  BMC Evol Biol       Date:  2019-11-06       Impact factor: 3.260

8.  Neural markers reveal a one-segmented head in tardigrades (water bears).

Authors:  Georg Mayer; Susann Kauschke; Jan Rüdiger; Paul A Stevenson
Journal:  PLoS One       Date:  2013-03-13       Impact factor: 3.240

  8 in total

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