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Johnston, R. E.

Publications and source records attributed to Johnston, R. E..

2 recordsLinked to original sources

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 of foraging effectively prevent young workers from partaking, we studied the biomechanical development of the bite apparatus in Atta vollenweideri leaf-cutter ants. Fully-matured foragers generate 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 may 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 mechanical demands on the musculoskeletal system.

developmental biology↗

A general biomechanical model for the relation between bite force and mandibular opening angle in arthropods

Bite forces play a key role in animal ecology: they affect mating behaviour, fighting success, and the ability to feed. Although feeding habits of arthropods have an enormous ecological and economical impact, we lack fundamental knowledge on how the morphology and physiology of their bite apparatus controls bite performance and its variation with mandible gape. To address this gap, we derived a comprehensive biomechanical model that characterises the relationship between bite force and mandibular opening angle from first principles. We validate the model by comparing its geometric predictions with morphological measurements on CT-scans of Atta cephalotes leaf-cutter ants. We then demonstrate its deductive and inductive power with three exemplary use cases: First, we extract the physiological properties of the leaf-cutter ant mandible closer muscle from in-vivo bite force measurements. Second, we show that leaf-cutter ants are extremely specialised for biting: they generate maximum bite forces equivalent to about 2600 times their body weight. Third, we discuss the relative importance of morphology and physiology in determining the magnitude and variation of bite force. We hope that our work will facilitate future comparative studies on the insect bite apparatus, and advance our knowledge of the behaviour, ecology and evolution of arthropods.

biophysics↗