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Developmental biomechanics and age polyethism in leaf-cutter ants
Many social insects display age polyethism: young workers stay inside the nest, and only older workers forage. This behavioural transition is accompanied by genetic and physiological changes, but the mechanistic origin of it remains unclear. To investigate if the mechanical demands on the musculoske...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265030/ https://www.ncbi.nlm.nih.gov/pubmed/37312549 http://dx.doi.org/10.1098/rspb.2023.0355 |
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author | Püffel, Frederik Meyer, Lara Imirzian, Natalie Roces, Flavio Johnston, Richard Labonte, David |
author_facet | Püffel, Frederik Meyer, Lara Imirzian, Natalie Roces, Flavio Johnston, Richard Labonte, David |
author_sort | Püffel, Frederik |
collection | PubMed |
description | Many social insects display age polyethism: young workers stay inside the nest, and only older workers forage. This behavioural transition is accompanied by genetic and physiological changes, but the mechanistic origin of it remains unclear. To investigate if the mechanical demands on the musculoskeletal system effectively prevent young workers from foraging, we studied the biomechanical development of the bite apparatus in Atta vollenweideri leaf-cutter ants. Fully matured foragers generated peak in vivo bite forces of around 100 mN, more than one order of magnitude in excess of those measured for freshly eclosed callows of the same size. This change in bite force was accompanied by a sixfold increase in the volume of the mandible closer muscle, and by a substantial increase of the flexural rigidity of the head capsule, driven by a significant increase in both average thickness and indentation modulus of the head capsule cuticle. Consequently, callows lack the muscle force capacity required for leaf-cutting, and their head capsule is so compliant that large muscle forces would be likely to cause damaging deformations. On the basis of these results, we speculate that continued biomechanical development post eclosion may be a key factor underlying age polyethism, wherever foraging is associated with substantial mechanical demands. |
format | Online Article Text |
id | pubmed-10265030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102650302023-06-15 Developmental biomechanics and age polyethism in leaf-cutter ants Püffel, Frederik Meyer, Lara Imirzian, Natalie Roces, Flavio Johnston, Richard Labonte, David Proc Biol Sci Morphology and Biomechanics Many social insects display age polyethism: young workers stay inside the nest, and only older workers forage. This behavioural transition is accompanied by genetic and physiological changes, but the mechanistic origin of it remains unclear. To investigate if the mechanical demands on the musculoskeletal system effectively prevent young workers from foraging, we studied the biomechanical development of the bite apparatus in Atta vollenweideri leaf-cutter ants. Fully matured foragers generated peak in vivo bite forces of around 100 mN, more than one order of magnitude in excess of those measured for freshly eclosed callows of the same size. This change in bite force was accompanied by a sixfold increase in the volume of the mandible closer muscle, and by a substantial increase of the flexural rigidity of the head capsule, driven by a significant increase in both average thickness and indentation modulus of the head capsule cuticle. Consequently, callows lack the muscle force capacity required for leaf-cutting, and their head capsule is so compliant that large muscle forces would be likely to cause damaging deformations. On the basis of these results, we speculate that continued biomechanical development post eclosion may be a key factor underlying age polyethism, wherever foraging is associated with substantial mechanical demands. The Royal Society 2023-06-14 2023-06-14 /pmc/articles/PMC10265030/ /pubmed/37312549 http://dx.doi.org/10.1098/rspb.2023.0355 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 | Morphology and Biomechanics Püffel, Frederik Meyer, Lara Imirzian, Natalie Roces, Flavio Johnston, Richard Labonte, David Developmental biomechanics and age polyethism in leaf-cutter ants |
title | Developmental biomechanics and age polyethism in leaf-cutter ants |
title_full | Developmental biomechanics and age polyethism in leaf-cutter ants |
title_fullStr | Developmental biomechanics and age polyethism in leaf-cutter ants |
title_full_unstemmed | Developmental biomechanics and age polyethism in leaf-cutter ants |
title_short | Developmental biomechanics and age polyethism in leaf-cutter ants |
title_sort | developmental biomechanics and age polyethism in leaf-cutter ants |
topic | Morphology and Biomechanics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265030/ https://www.ncbi.nlm.nih.gov/pubmed/37312549 http://dx.doi.org/10.1098/rspb.2023.0355 |
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