Abstract

BackgroundThough some elements of the bryozoan nervous system were discovered 180 years ago, few studies of their neuromorphology have been undertaken since that time. As a result the general picture of the bryozoan nervous system structure is incomplete in respect of details and fragmentary in respect of taxonomic coverage.ResultsThe nervous system of three common European freshwater bryozoans – Cristatella mucedo, Plumatella repens (both with a horseshoe-shaped lophophore) and Fredericella sultana (with a circular lophophore) had numerous differences in the details of the structure but the general neuroarchitecture is similar. The nervous system of the zooid consists of the cerebral ganglion, a circumpharyngeal ring and lophophoral nerve tracts (horns), both sending numerous nerves to the tentacles, and the nerve plexuses of the body wall and of the gut. A number of the important details (distal branching of the additional radial nerve, pattern of distribution of nerve cells and neurites in the ganglion, etc.) were described for the first time. The number and position of the tentacle nerves in Cristatella mucedo was ascertained and suggestions about their function were made. The revealed distribution of various neuromediators in the nervous system allowed us to suggest functional affinities of some major nerves.ConclusionsDespite the basic similarity, both the ganglion and the lophophore nervous system in Phylactolaemata have a more complex structure than in marine bryozoans (classes Gymnolaemata and Stenolaemata). First of all, their neuronal network has a denser and more complex branching pattern: most phylactolaemates have two large nerve tracts associated with lophophore arms, they have more nerves in the tentacles, additional and basal branches emitting from the main radial nerves, etc. This, in part, can be explained by the horseshoe shape of the lophophore and a larger size of the polypide in freshwater species. The structure of the nervous system in Fredericella sultana suggests that it underwent a secondary simplification following the reduction of the lophophore arms. Colony locomotion in Cristatella mucedo is based on co-ordinated activity of two perpendicular muscle layers of the sole and the plexus of motor neurons sandwiched between them. The trigger of this activity and the co-ordination mechanism remain enigmatic.Electronic supplementary materialThe online version of this article (doi:10.1186/s12983-015-0112-2) contains supplementary material, which is available to authorized users.

Highlights

  • Bryozoans are sessile filter-feeding invertebrates whose sheet-like, bushy or arborescent colonies are abundant in various freshwater and marine bottom habitats, from rivers and lakes to a shallow subtidal and oceanic abyss

  • Whereas polypides of C. mucedo and P. repens have a horseshoe-shaped lophophore with 30–60 tentacles, F. sultana has a small bell-shaped lophophore similar to that in marine bryozoans

  • Lophophore Our data considerably added to the existing knowledge of the topography and gross morphology of the nervous system in phylactolaemate bryozoans (Figs. 15, 16)

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Summary

Introduction

Bryozoans are sessile filter-feeding invertebrates whose sheet-like, bushy or arborescent colonies are abundant in various freshwater and marine bottom habitats, from rivers and lakes to a shallow subtidal and oceanic abyss. Each bryozoan colony consists of interconnected modules, zooids, which are formally subdivided into the polypide – a protruding ciliated tentacle crown (lophophore) with a digestive tract and associated musculature and the cystid – the receptacle of the polypide. The external layer (ectocyst) of the cystid wall of marine bryozoans (classes Gymnolaemata and Stenolaemata) can be calcified or chitinous, whereas in the freshwater class Phylactolaemata it is chitinous or gelatinous. In gymno- and Shunkina et al Frontiers in Zoology (2015) 12:28 stenolaemates the muscle layers and, sometimes, peritoneal lining are missing. Both gymnolaemates and stenolaemates possess a bell-shaped tentacle crown with a central mouth, the tentacle bases forming a circle around it. As a result the general picture of the bryozoan nervous system structure is incomplete in respect of details and fragmentary in respect of taxonomic coverage

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