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Off like a shot: scaling of ballistic tongue projection reveals extremely high performance in small chameleons
Stretching elastic tissues and using their recoil to power movement allows organisms to release energy more rapidly than by muscle contraction directly, thus amplifying power output. Chameleons employ such a mechanism to ballistically project their tongue up to two body lengths, achieving power outp...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4698635/ https://www.ncbi.nlm.nih.gov/pubmed/26725508 http://dx.doi.org/10.1038/srep18625 |
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author | Anderson, Christopher V. |
author_facet | Anderson, Christopher V. |
author_sort | Anderson, Christopher V. |
collection | PubMed |
description | Stretching elastic tissues and using their recoil to power movement allows organisms to release energy more rapidly than by muscle contraction directly, thus amplifying power output. Chameleons employ such a mechanism to ballistically project their tongue up to two body lengths, achieving power outputs nearly three times greater than those possible via muscle contraction. Additionally, small organisms tend to be capable of greater performance than larger species performing similar movements. To test the hypothesis that small chameleon species outperform larger species during ballistic tongue projection, performance was examined during feeding among 20 chameleon species in nine genera. This revealed that small species project their tongues proportionately further than large species, achieving projection distances of 2.5 body lengths. Furthermore, feedings with peak accelerations of 2,590 m s(−2), or 264 g, and peak power output values of 14,040 W kg(−1) are reported. These values represent the highest accelerations and power outputs reported for any amniote movement, highlighting the previously underestimated performance capability of the family. These findings show that examining movements in smaller animals may expose movements harbouring cryptic power amplification mechanisms and illustrate how varying metabolic demands may help drive morphological evolution. |
format | Online Article Text |
id | pubmed-4698635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46986352016-01-13 Off like a shot: scaling of ballistic tongue projection reveals extremely high performance in small chameleons Anderson, Christopher V. Sci Rep Article Stretching elastic tissues and using their recoil to power movement allows organisms to release energy more rapidly than by muscle contraction directly, thus amplifying power output. Chameleons employ such a mechanism to ballistically project their tongue up to two body lengths, achieving power outputs nearly three times greater than those possible via muscle contraction. Additionally, small organisms tend to be capable of greater performance than larger species performing similar movements. To test the hypothesis that small chameleon species outperform larger species during ballistic tongue projection, performance was examined during feeding among 20 chameleon species in nine genera. This revealed that small species project their tongues proportionately further than large species, achieving projection distances of 2.5 body lengths. Furthermore, feedings with peak accelerations of 2,590 m s(−2), or 264 g, and peak power output values of 14,040 W kg(−1) are reported. These values represent the highest accelerations and power outputs reported for any amniote movement, highlighting the previously underestimated performance capability of the family. These findings show that examining movements in smaller animals may expose movements harbouring cryptic power amplification mechanisms and illustrate how varying metabolic demands may help drive morphological evolution. Nature Publishing Group 2016-01-04 /pmc/articles/PMC4698635/ /pubmed/26725508 http://dx.doi.org/10.1038/srep18625 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Anderson, Christopher V. Off like a shot: scaling of ballistic tongue projection reveals extremely high performance in small chameleons |
title | Off like a shot: scaling of ballistic tongue projection reveals extremely high performance in small chameleons |
title_full | Off like a shot: scaling of ballistic tongue projection reveals extremely high performance in small chameleons |
title_fullStr | Off like a shot: scaling of ballistic tongue projection reveals extremely high performance in small chameleons |
title_full_unstemmed | Off like a shot: scaling of ballistic tongue projection reveals extremely high performance in small chameleons |
title_short | Off like a shot: scaling of ballistic tongue projection reveals extremely high performance in small chameleons |
title_sort | off like a shot: scaling of ballistic tongue projection reveals extremely high performance in small chameleons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4698635/ https://www.ncbi.nlm.nih.gov/pubmed/26725508 http://dx.doi.org/10.1038/srep18625 |
work_keys_str_mv | AT andersonchristopherv offlikeashotscalingofballistictongueprojectionrevealsextremelyhighperformanceinsmallchameleons |