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Echolocating toothed whales use ultra-fast echo-kinetic responses to track evasive prey

Visual predators rely on fast-acting optokinetic responses to track and capture agile prey. Most toothed whales, however, rely on echolocation for hunting and have converged on biosonar clicking rates reaching 500/s during prey pursuits. If echoes are processed on a click-by-click basis, as assumed,...

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Autores principales: Vance, Heather, Madsen, Peter T, Aguilar de Soto, Natacha, Wisniewska, Danuta Maria, Ladegaard, Michael, Hooker, Sascha, Johnson, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547948/
https://www.ncbi.nlm.nih.gov/pubmed/34696826
http://dx.doi.org/10.7554/eLife.68825
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author Vance, Heather
Madsen, Peter T
Aguilar de Soto, Natacha
Wisniewska, Danuta Maria
Ladegaard, Michael
Hooker, Sascha
Johnson, Mark
author_facet Vance, Heather
Madsen, Peter T
Aguilar de Soto, Natacha
Wisniewska, Danuta Maria
Ladegaard, Michael
Hooker, Sascha
Johnson, Mark
author_sort Vance, Heather
collection PubMed
description Visual predators rely on fast-acting optokinetic responses to track and capture agile prey. Most toothed whales, however, rely on echolocation for hunting and have converged on biosonar clicking rates reaching 500/s during prey pursuits. If echoes are processed on a click-by-click basis, as assumed, neural responses 100× faster than those in vision are required to keep pace with this information flow. Using high-resolution biologging of wild predator-prey interactions, we show that toothed whales adjust clicking rates to track prey movement within 50–200 ms of prey escape responses. Hypothesising that these stereotyped biosonar adjustments are elicited by sudden prey accelerations, we measured echo-kinetic responses from trained harbour porpoises to a moving target and found similar latencies. High biosonar sampling rates are, therefore, not supported by extreme speeds of neural processing and muscular responses. Instead, the neurokinetic response times in echolocation are similar to those of tracking responses in vision, suggesting a common neural underpinning.
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spelling pubmed-85479482021-10-27 Echolocating toothed whales use ultra-fast echo-kinetic responses to track evasive prey Vance, Heather Madsen, Peter T Aguilar de Soto, Natacha Wisniewska, Danuta Maria Ladegaard, Michael Hooker, Sascha Johnson, Mark eLife Ecology Visual predators rely on fast-acting optokinetic responses to track and capture agile prey. Most toothed whales, however, rely on echolocation for hunting and have converged on biosonar clicking rates reaching 500/s during prey pursuits. If echoes are processed on a click-by-click basis, as assumed, neural responses 100× faster than those in vision are required to keep pace with this information flow. Using high-resolution biologging of wild predator-prey interactions, we show that toothed whales adjust clicking rates to track prey movement within 50–200 ms of prey escape responses. Hypothesising that these stereotyped biosonar adjustments are elicited by sudden prey accelerations, we measured echo-kinetic responses from trained harbour porpoises to a moving target and found similar latencies. High biosonar sampling rates are, therefore, not supported by extreme speeds of neural processing and muscular responses. Instead, the neurokinetic response times in echolocation are similar to those of tracking responses in vision, suggesting a common neural underpinning. eLife Sciences Publications, Ltd 2021-10-26 /pmc/articles/PMC8547948/ /pubmed/34696826 http://dx.doi.org/10.7554/eLife.68825 Text en © 2021, Vance et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Ecology
Vance, Heather
Madsen, Peter T
Aguilar de Soto, Natacha
Wisniewska, Danuta Maria
Ladegaard, Michael
Hooker, Sascha
Johnson, Mark
Echolocating toothed whales use ultra-fast echo-kinetic responses to track evasive prey
title Echolocating toothed whales use ultra-fast echo-kinetic responses to track evasive prey
title_full Echolocating toothed whales use ultra-fast echo-kinetic responses to track evasive prey
title_fullStr Echolocating toothed whales use ultra-fast echo-kinetic responses to track evasive prey
title_full_unstemmed Echolocating toothed whales use ultra-fast echo-kinetic responses to track evasive prey
title_short Echolocating toothed whales use ultra-fast echo-kinetic responses to track evasive prey
title_sort echolocating toothed whales use ultra-fast echo-kinetic responses to track evasive prey
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547948/
https://www.ncbi.nlm.nih.gov/pubmed/34696826
http://dx.doi.org/10.7554/eLife.68825
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