ArticleThe Journal of comparative neurology2020
Neuroanatomical and neurophysiological mechanisms of acoustic and weakly electric signaling in synodontid catfish.
Article in The Journal of comparative neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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7 citing papers in PubMed.
- Variation in behavioral preference and calcium binding expression in twoFrontiers in neuroanatomy · 2025Article
- Article
- Reconstruction of Electric Discharge Patterns and Electrogenesis Mechanism in African Sharptooth Catfish Clarias gariepinus (Clariidae, Siluriformes).Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections · 2021Article
- Morphological diversity of acoustic and electric communication systems of mochokid catfish.The Journal of comparative neurology · 2021Article
- Gap junction-mediated glycinergic inhibition ensures precise temporal patterning in vocal behavior.eLife · 2021Article
- Vocal and Electric Fish: Revisiting a Comparison of Two Teleost Models in the Neuroethology of Social Behavior.Frontiers in neural circuits · 2021Review
- Neuroanatomical and neurophysiological mechanisms of acoustic and weakly electric signaling in synodontid catfish.The Journal of comparative neurology · 2020Article
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4 authors.
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Abstract
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.
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