Cargando…

Neuroanatomical and neurophysiological mechanisms of acoustic and weakly electric signaling in synodontid catfish

To what extent do modifications in the nervous system and peripheral effectors contribute to novel behaviors? Using a combination of morphometric analysis, neuroanatomical tract‐tracing, and intracellular neuronal recording, we address this question in a sound‐producing and a weakly electric species...

Descripción completa

Detalles Bibliográficos
Autores principales: Kéver, Loïc, Bass, Andrew H., Parmentier, Eric, Chagnaud, Boris P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496807/
https://www.ncbi.nlm.nih.gov/pubmed/32266714
http://dx.doi.org/10.1002/cne.24920
_version_ 1783583179338153984
author Kéver, Loïc
Bass, Andrew H.
Parmentier, Eric
Chagnaud, Boris P.
author_facet Kéver, Loïc
Bass, Andrew H.
Parmentier, Eric
Chagnaud, Boris P.
author_sort Kéver, Loïc
collection PubMed
description To what extent do modifications in the nervous system and peripheral effectors contribute to novel behaviors? Using a combination of morphometric analysis, neuroanatomical tract‐tracing, and intracellular neuronal recording, we address this question in a sound‐producing and a weakly electric species of synodontid catfish, Synodontis grandiops, and Synodontis nigriventris, respectively. The same peripheral mechanism, a bilateral pair of protractor muscles associated with vertebral processes (elastic spring mechanism), is involved in both signaling systems. Although there were dramatic species differences in several morphometric measures, electromyograms provided strong evidence that simultaneous activation of paired protractor muscles accounts for an individual sound and electric discharge pulse. While the general architecture of the neural network and the intrinsic properties of the motoneuron population driving each target was largely similar, differences could contribute to species‐specific patterns in electromyograms and the associated pulse repetition rate of sounds and electric discharges. Together, the results suggest that adaptive changes in both peripheral and central characters underlie the transition from an ancestral sound to a derived electric discharge producing system, and thus the evolution of a novel communication channel among synodontid catfish. Similarities with characters in other sonic and weakly electric teleost fish provide a striking example of convergent evolution in functional adaptations underlying the evolution of the two signaling systems among distantly related taxa.
format Online
Article
Text
id pubmed-7496807
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-74968072020-09-25 Neuroanatomical and neurophysiological mechanisms of acoustic and weakly electric signaling in synodontid catfish Kéver, Loïc Bass, Andrew H. Parmentier, Eric Chagnaud, Boris P. J Comp Neurol Research Articles To what extent do modifications in the nervous system and peripheral effectors contribute to novel behaviors? Using a combination of morphometric analysis, neuroanatomical tract‐tracing, and intracellular neuronal recording, we address this question in a sound‐producing and a weakly electric species of synodontid catfish, Synodontis grandiops, and Synodontis nigriventris, respectively. The same peripheral mechanism, a bilateral pair of protractor muscles associated with vertebral processes (elastic spring mechanism), is involved in both signaling systems. Although there were dramatic species differences in several morphometric measures, electromyograms provided strong evidence that simultaneous activation of paired protractor muscles accounts for an individual sound and electric discharge pulse. While the general architecture of the neural network and the intrinsic properties of the motoneuron population driving each target was largely similar, differences could contribute to species‐specific patterns in electromyograms and the associated pulse repetition rate of sounds and electric discharges. Together, the results suggest that adaptive changes in both peripheral and central characters underlie the transition from an ancestral sound to a derived electric discharge producing system, and thus the evolution of a novel communication channel among synodontid catfish. Similarities with characters in other sonic and weakly electric teleost fish provide a striking example of convergent evolution in functional adaptations underlying the evolution of the two signaling systems among distantly related taxa. John Wiley & Sons, Inc. 2020-04-21 2020-10-15 /pmc/articles/PMC7496807/ /pubmed/32266714 http://dx.doi.org/10.1002/cne.24920 Text en © 2020 The Authors. The Journal of Comparative Neurology published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Kéver, Loïc
Bass, Andrew H.
Parmentier, Eric
Chagnaud, Boris P.
Neuroanatomical and neurophysiological mechanisms of acoustic and weakly electric signaling in synodontid catfish
title Neuroanatomical and neurophysiological mechanisms of acoustic and weakly electric signaling in synodontid catfish
title_full Neuroanatomical and neurophysiological mechanisms of acoustic and weakly electric signaling in synodontid catfish
title_fullStr Neuroanatomical and neurophysiological mechanisms of acoustic and weakly electric signaling in synodontid catfish
title_full_unstemmed Neuroanatomical and neurophysiological mechanisms of acoustic and weakly electric signaling in synodontid catfish
title_short Neuroanatomical and neurophysiological mechanisms of acoustic and weakly electric signaling in synodontid catfish
title_sort neuroanatomical and neurophysiological mechanisms of acoustic and weakly electric signaling in synodontid catfish
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496807/
https://www.ncbi.nlm.nih.gov/pubmed/32266714
http://dx.doi.org/10.1002/cne.24920
work_keys_str_mv AT keverloic neuroanatomicalandneurophysiologicalmechanismsofacousticandweaklyelectricsignalinginsynodontidcatfish
AT bassandrewh neuroanatomicalandneurophysiologicalmechanismsofacousticandweaklyelectricsignalinginsynodontidcatfish
AT parmentiereric neuroanatomicalandneurophysiologicalmechanismsofacousticandweaklyelectricsignalinginsynodontidcatfish
AT chagnaudborisp neuroanatomicalandneurophysiologicalmechanismsofacousticandweaklyelectricsignalinginsynodontidcatfish