Sl. Katz et Jm. Gosline, ONTOGENIC SCALING OF JUMP PERFORMANCE IN THE AFRICAN DESERT LOCUST (SCHISTOCERCA-GREGARIA), Journal of Experimental Biology, 177, 1993, pp. 81-111
Ontogenetic growth was used as a model for the effect of body size on
jumping performance of the African desert locust (Schistocerca gregari
a). Using models that generated relationships between morphology and b
ody size proposed by McMahon and the relationships between morphology
and performance described by Hill, we generated testable predictions o
f how jumping performance measures may change as a function of body ma
ss. Data were collected over an ontogenetic sequence that ranged from
1-day-old first instars to 45-day-old adults. Performance was quantifi
ed using a high-sensitivity, three-dimensional force plate. Performanc
e parameters quantified included the force, acceleration, take-off vel
ocity, kinetic energy and power output. With the exception of power ou
tput, each measure of performance scaled to body mass in a manner cons
istent with the predictions of the elastic similarity model. Power out
put scaled to body mass in a manner consistent with the predictions of
the constant stress similarity model. As we noted previously for the
scaling of flexural stiffness of the metathoracic tibiae, the elastic
similarity model is approximated by the performance of the locust in s
pite of the morphological design that deviates from that model's predi
ctions. These results indicate that the jump has separate functions in
the flightless juvenile instars and in the flying adult stage of the
life history. Juvenile locusts produce take-off velocities of between
0.9 and 1.2 m s-1 that are relatively scale-independent. The take-off
velocity in juveniles produces a distance of ballistic travel that ave
rages between 20 and 30 cm. In adults, the take-off velocity is also r
elatively scale-independent at a level approximately twice as high as
in juveniles (i.e. 2.5 m s-1). This velocity is coincident with the mi
nimum flight speed reported by Weis-Fogh and a minimum flight speed th
at we have estimated using actuator disc theory. We suggest that, in j
uveniles, the jump is designed to achieve a characteristic distance tr
avelled and in adults the jump is designed to achieve a minimum veloci
ty necessary to fly.