Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

Is the Capacity for Vocal Learning in Vertebrates Rooted in Fish Schooling Behavior?

Larsson, Matz LU and Abbott, Benjamin W. (2018) In Evolutionary Biology 45(4). p.359-373
Abstract

The capacity to learn and reproduce vocal sounds has evolved in phylogenetically distant tetrapod lineages. Vocal learners in all these lineages express similar neural circuitry and genetic factors when perceiving, processing, and reproducing vocalization, suggesting that brain pathways for vocal learning evolved within strong constraints from a common ancestor, potentially fish. We hypothesize that the auditory-motor circuits and genes involved in entrainment have their origins in fish schooling behavior and respiratory-motor coupling. In this acoustic advantages hypothesis, aural costs and benefits played a key role in shaping a wide variety of traits, which could readily be exapted for entrainment and vocal learning, including social... (More)

The capacity to learn and reproduce vocal sounds has evolved in phylogenetically distant tetrapod lineages. Vocal learners in all these lineages express similar neural circuitry and genetic factors when perceiving, processing, and reproducing vocalization, suggesting that brain pathways for vocal learning evolved within strong constraints from a common ancestor, potentially fish. We hypothesize that the auditory-motor circuits and genes involved in entrainment have their origins in fish schooling behavior and respiratory-motor coupling. In this acoustic advantages hypothesis, aural costs and benefits played a key role in shaping a wide variety of traits, which could readily be exapted for entrainment and vocal learning, including social grouping, group movement, and respiratory-motor coupling. Specifically, incidental sounds of locomotion and respiration (ISLR) may have reinforced synchronization by communicating important spatial and temporal information between school-members and extending windows of silence to improve situational awareness. This process would be mutually reinforcing. Neurons in the telencephalon, which were initially involved in linking ISLR with forelimbs, could have switched functions to serve vocal machinery (e.g. mouth, beak, tongue, larynx, syrinx). While previous vocal learning hypotheses invoke transmission of neurons from visual tasks (gestures) to the auditory channel, this hypothesis involves the auditory channel from the onset. Acoustic benefits of locomotor-respiratory coordination in fish may have selected for genetic factors and brain circuitry capable of synchronizing respiratory and limb movements, predisposing tetrapod lines to synchronized movement, vocalization, and vocal learning. We discuss how the capacity to entrain is manifest in fish, amphibians, birds, and mammals, and propose predictions to test our acoustic advantages hypothesis.

(Less)
Please use this url to cite or link to this publication:
author
and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Entrainment, Fish schooling, FoxP2, Incidental sound, Locomotion, Locomotor-respiratory coupling, Respiration, Synchronization, Vocal learning
in
Evolutionary Biology
volume
45
issue
4
pages
359 - 373
publisher
Springer
external identifiers
  • scopus:85048491612
  • pmid:30459479
ISSN
0071-3260
DOI
10.1007/s11692-018-9457-8
language
English
LU publication?
yes
id
18088aa3-355c-4502-afcf-326230669d3b
date added to LUP
2018-06-28 15:22:15
date last changed
2024-04-15 08:45:43
@article{18088aa3-355c-4502-afcf-326230669d3b,
  abstract     = {{<p>The capacity to learn and reproduce vocal sounds has evolved in phylogenetically distant tetrapod lineages. Vocal learners in all these lineages express similar neural circuitry and genetic factors when perceiving, processing, and reproducing vocalization, suggesting that brain pathways for vocal learning evolved within strong constraints from a common ancestor, potentially fish. We hypothesize that the auditory-motor circuits and genes involved in entrainment have their origins in fish schooling behavior and respiratory-motor coupling. In this acoustic advantages hypothesis, aural costs and benefits played a key role in shaping a wide variety of traits, which could readily be exapted for entrainment and vocal learning, including social grouping, group movement, and respiratory-motor coupling. Specifically, incidental sounds of locomotion and respiration (ISLR) may have reinforced synchronization by communicating important spatial and temporal information between school-members and extending windows of silence to improve situational awareness. This process would be mutually reinforcing. Neurons in the telencephalon, which were initially involved in linking ISLR with forelimbs, could have switched functions to serve vocal machinery (e.g. mouth, beak, tongue, larynx, syrinx). While previous vocal learning hypotheses invoke transmission of neurons from visual tasks (gestures) to the auditory channel, this hypothesis involves the auditory channel from the onset. Acoustic benefits of locomotor-respiratory coordination in fish may have selected for genetic factors and brain circuitry capable of synchronizing respiratory and limb movements, predisposing tetrapod lines to synchronized movement, vocalization, and vocal learning. We discuss how the capacity to entrain is manifest in fish, amphibians, birds, and mammals, and propose predictions to test our acoustic advantages hypothesis.</p>}},
  author       = {{Larsson, Matz and Abbott, Benjamin W.}},
  issn         = {{0071-3260}},
  keywords     = {{Entrainment; Fish schooling; FoxP2; Incidental sound; Locomotion; Locomotor-respiratory coupling; Respiration; Synchronization; Vocal learning}},
  language     = {{eng}},
  number       = {{4}},
  pages        = {{359--373}},
  publisher    = {{Springer}},
  series       = {{Evolutionary Biology}},
  title        = {{Is the Capacity for Vocal Learning in Vertebrates Rooted in Fish Schooling Behavior?}},
  url          = {{http://dx.doi.org/10.1007/s11692-018-9457-8}},
  doi          = {{10.1007/s11692-018-9457-8}},
  volume       = {{45}},
  year         = {{2018}},
}