Abstract

ABSTRACTMany insects such as fleas, froghoppers and grasshoppers use a catapult mechanism to jump, and a direct consequence of this is that their take-off velocities are independent of their mass. In contrast, insects such as mantises, caddis flies and bush crickets propel their jumps by direct muscle contractions. What constrains the jumping performance of insects that use this second mechanism? To answer this question, the jumping performance of the mantis Stagmomantis theophila was measured through all its developmental stages, from 5 mg first instar nymphs to 1200 mg adults. Older and heavier mantises have longer hind and middle legs and higher take-off velocities than younger and lighter mantises. The length of the propulsive hind and middle legs scaled approximately isometrically with body mass (exponent=0.29 and 0.32, respectively). The front legs, which do not contribute to propulsion, scaled with an exponent of 0.37. Take-off velocity increased with increasing body mass (exponent=0.12). Time to accelerate increased and maximum acceleration decreased, but the measured power that a given mass of jumping muscle produced remained constant throughout all stages. Mathematical models were used to distinguish between three possible limitations to the scaling relationships: first, an energy-limited model (which explains catapult jumpers); second, a power-limited model; and third, an acceleration-limited model. Only the model limited by muscle power explained the experimental data. Therefore, the two biomechanical mechanisms impose different limitations on jumping: those involving direct muscle contractions (mantises) are constrained by muscle power, whereas those involving catapult mechanisms are constrained by muscle energy.

Highlights

  • Many insects are powerful jumpers, with the best able to reach takeoff velocities as high as 5 m s−1 in acceleration times of less than 1 ms (Burrows, 2003, 2006, 2009)

  • Leg and body lengths indicate that mantises grow isometrically If take-off velocity is constrained by the energy that a muscle produces, as in catapult jumping mechanisms, it should not be affected by the length of the propulsive legs (Alexander, 1995)

  • As mantises grew across all developmental stages (Fig. 1A), the lengths of the hind and middle legs, which generate jumping, both scaled isometrically with body mass: hind legs with an exponent of 0.29 (R2=0.87, P=7×10−20, F=533, N=43; Fig. 1B), middle legs with an exponent of 0.32 (R2=0.95, P=1.2×10−28, F=772, N=43; Fig. 1C)

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Summary

Introduction

Many insects are powerful jumpers, with the best able to reach takeoff velocities as high as 5 m s−1 in acceleration times of less than 1 ms (Burrows, 2003, 2006, 2009). The spring recoils rapidly, releasing the stored energy and delivering considerable power (energy/time) to the legs, which propel the insect into the air (Bennet-Clark and Lucey, 1967; Patek et al, 2011) As mass increases, these insects will have a greater amount of available energy but will have correspondingly larger opposing inertia. An equivalent increase in both available energy and inertia will result in the take-off velocity (and the maximum jumping height) being independent of mass This relationship was formulated as ‘Borelli’s law’ in the 17th century (Borelli, 1680) and summarised by Bobbert (2013). The take-off velocity of jumps using a catapult mechanism is restricted by the energy a given mass of muscle can produce and store in the spring (Alexander, 1995; Vogel, 2005b)

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