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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...

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Autores principales: Püffel, Frederik, Meyer, Lara, Imirzian, Natalie, Roces, Flavio, Johnston, Richard, Labonte, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
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.
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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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