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Experimental studies suggest differences in the distribution of thorax elasticity between insects with synchronous and asynchronous musculature

Insects have developed diverse flight actuation mechanisms, including synchronous and asynchronous musculature. Indirect actuation, used by insects with both synchronous and asynchronous musculature, transforms thorax exoskeletal deformation into wing rotation. Though thorax deformation is often att...

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Autores principales: Casey, Cailin, Heveran, Chelsea, Jankauski, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10072941/
https://www.ncbi.nlm.nih.gov/pubmed/37015268
http://dx.doi.org/10.1098/rsif.2023.0029
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author Casey, Cailin
Heveran, Chelsea
Jankauski, Mark
author_facet Casey, Cailin
Heveran, Chelsea
Jankauski, Mark
author_sort Casey, Cailin
collection PubMed
description Insects have developed diverse flight actuation mechanisms, including synchronous and asynchronous musculature. Indirect actuation, used by insects with both synchronous and asynchronous musculature, transforms thorax exoskeletal deformation into wing rotation. Though thorax deformation is often attributed exclusively to muscle tension, the inertial and aerodynamic forces generated by the flapping wings may also contribute. In this study, a tethered flight experiment was used to simultaneously measure thorax deformation and the inertial/aerodynamic forces acting on the thorax generated by the flapping wing. Compared to insects with synchronous musculature, insects with asynchronous muscle deformed their thorax 60% less relative to their thorax diameter and their wings generated 2.8 times greater forces relative to their body weight. In a second experiment, dorsalventral thorax stiffness was measured across species. Accounting for weight and size, the asynchronous thorax was on average 3.8 times stiffer than the synchronous thorax in the dorsalventral direction. Differences in thorax stiffness and forces acting at the wing hinge led us to hypothesize about differing roles of series and parallel elasticity in the thoraxes of insects with synchronous and asynchronous musculature. Specifically, wing hinge elasticity may contribute more to wing motion in insects with asynchronous musculature than in those with synchronous musculature.
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spelling pubmed-100729412023-04-05 Experimental studies suggest differences in the distribution of thorax elasticity between insects with synchronous and asynchronous musculature Casey, Cailin Heveran, Chelsea Jankauski, Mark J R Soc Interface Life Sciences–Engineering interface Insects have developed diverse flight actuation mechanisms, including synchronous and asynchronous musculature. Indirect actuation, used by insects with both synchronous and asynchronous musculature, transforms thorax exoskeletal deformation into wing rotation. Though thorax deformation is often attributed exclusively to muscle tension, the inertial and aerodynamic forces generated by the flapping wings may also contribute. In this study, a tethered flight experiment was used to simultaneously measure thorax deformation and the inertial/aerodynamic forces acting on the thorax generated by the flapping wing. Compared to insects with synchronous musculature, insects with asynchronous muscle deformed their thorax 60% less relative to their thorax diameter and their wings generated 2.8 times greater forces relative to their body weight. In a second experiment, dorsalventral thorax stiffness was measured across species. Accounting for weight and size, the asynchronous thorax was on average 3.8 times stiffer than the synchronous thorax in the dorsalventral direction. Differences in thorax stiffness and forces acting at the wing hinge led us to hypothesize about differing roles of series and parallel elasticity in the thoraxes of insects with synchronous and asynchronous musculature. Specifically, wing hinge elasticity may contribute more to wing motion in insects with asynchronous musculature than in those with synchronous musculature. The Royal Society 2023-04-05 /pmc/articles/PMC10072941/ /pubmed/37015268 http://dx.doi.org/10.1098/rsif.2023.0029 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Life Sciences–Engineering interface
Casey, Cailin
Heveran, Chelsea
Jankauski, Mark
Experimental studies suggest differences in the distribution of thorax elasticity between insects with synchronous and asynchronous musculature
title Experimental studies suggest differences in the distribution of thorax elasticity between insects with synchronous and asynchronous musculature
title_full Experimental studies suggest differences in the distribution of thorax elasticity between insects with synchronous and asynchronous musculature
title_fullStr Experimental studies suggest differences in the distribution of thorax elasticity between insects with synchronous and asynchronous musculature
title_full_unstemmed Experimental studies suggest differences in the distribution of thorax elasticity between insects with synchronous and asynchronous musculature
title_short Experimental studies suggest differences in the distribution of thorax elasticity between insects with synchronous and asynchronous musculature
title_sort experimental studies suggest differences in the distribution of thorax elasticity between insects with synchronous and asynchronous musculature
topic Life Sciences–Engineering interface
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10072941/
https://www.ncbi.nlm.nih.gov/pubmed/37015268
http://dx.doi.org/10.1098/rsif.2023.0029
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