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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ftdoajarticles:oai:doaj.org/article:bec0e83099c748c5b239b719fca69f4c 2023-05-15T16:33:25+02:00 Echolocating toothed whales use ultra-fast echo-kinetic responses to track evasive prey Heather Vance Peter T Madsen Natacha Aguilar de Soto Danuta Maria Wisniewska Michael Ladegaard Sascha Hooker Mark Johnson 2021-10-01T00:00:00Z https://doi.org/10.7554/eLife.68825 https://doaj.org/article/bec0e83099c748c5b239b719fca69f4c EN eng eLife Sciences Publications Ltd https://elifesciences.org/articles/68825 https://doaj.org/toc/2050-084X doi:10.7554/eLife.68825 2050-084X e68825 https://doaj.org/article/bec0e83099c748c5b239b719fca69f4c eLife, Vol 10 (2021) echolocation biosonar harbour porpoise blainville's beaked whale predator-prey interactions response latency Medicine R Science Q Biology (General) QH301-705.5 article 2021 ftdoajarticles https://doi.org/10.7554/eLife.68825 2022-12-31T00:08:16Z 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. Article in Journal/Newspaper Harbour porpoise toothed whales Directory of Open Access Journals: DOAJ Articles eLife 10 |
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Open Polar |
collection |
Directory of Open Access Journals: DOAJ Articles |
op_collection_id |
ftdoajarticles |
language |
English |
topic |
echolocation biosonar harbour porpoise blainville's beaked whale predator-prey interactions response latency Medicine R Science Q Biology (General) QH301-705.5 |
spellingShingle |
echolocation biosonar harbour porpoise blainville's beaked whale predator-prey interactions response latency Medicine R Science Q Biology (General) QH301-705.5 Heather Vance Peter T Madsen Natacha Aguilar de Soto Danuta Maria Wisniewska Michael Ladegaard Sascha Hooker Mark Johnson Echolocating toothed whales use ultra-fast echo-kinetic responses to track evasive prey |
topic_facet |
echolocation biosonar harbour porpoise blainville's beaked whale predator-prey interactions response latency Medicine R Science Q Biology (General) QH301-705.5 |
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. |
format |
Article in Journal/Newspaper |
author |
Heather Vance Peter T Madsen Natacha Aguilar de Soto Danuta Maria Wisniewska Michael Ladegaard Sascha Hooker Mark Johnson |
author_facet |
Heather Vance Peter T Madsen Natacha Aguilar de Soto Danuta Maria Wisniewska Michael Ladegaard Sascha Hooker Mark Johnson |
author_sort |
Heather Vance |
title |
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_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_sort |
echolocating toothed whales use ultra-fast echo-kinetic responses to track evasive prey |
publisher |
eLife Sciences Publications Ltd |
publishDate |
2021 |
url |
https://doi.org/10.7554/eLife.68825 https://doaj.org/article/bec0e83099c748c5b239b719fca69f4c |
genre |
Harbour porpoise toothed whales |
genre_facet |
Harbour porpoise toothed whales |
op_source |
eLife, Vol 10 (2021) |
op_relation |
https://elifesciences.org/articles/68825 https://doaj.org/toc/2050-084X doi:10.7554/eLife.68825 2050-084X e68825 https://doaj.org/article/bec0e83099c748c5b239b719fca69f4c |
op_doi |
https://doi.org/10.7554/eLife.68825 |
container_title |
eLife |
container_volume |
10 |
_version_ |
1766023107557982208 |