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J Camhi

Publications and source records attributed to J Camhi.

4 recordsLinked to original sources

Producing directed behaviour: muscle activity patterns of the cockroach escape response

The cockroach responds to wind from the front left by making an escape turn to the right, and vice versa. So far, no interneurones in the escape system are known that respond only to wind from the left or only to wind from the right. In this study, we used electromyographic recordings to determine whether motor neurones respond in this direction-selective manner during escape behaviour. In the mesothoracic coxal-femoral joint, whose movement direction is diagnostic for escape direction, the fast motor neurones of one muscle respond selectively to one wind direction, and those of the antagonistic muscle respond selectively to wind from the other direction, resulting in an appropriate turning response. This rules out an alternative hypothesis, a co-activation mechanism of specifying turn direction. These results suggest that it would be fruitful to search among the interneurones of the escape system for additional cells and circuit properties that could give rise to this sharp directional discrimination.

Journal Article

Wing-beat coupling between flying locust pairs: preferred phase and lift enhancement

Pairs of locusts flying in tandem in a wind tunnel are known to couple their wing-beats intermittently. The rhythmically oscillating air flow from the front locust's wing-beat, detected by the rear individual, appears to convey the timing information for coupling. Three predictions of this arrangement were tested quantitatively in this study. (1) Given that the oscillating air flow has a wavelength of 7.5 cm, placing the rear locust 7.5 or 15 cm behind the front one should produce the same phase of coupling, whereas placing it at an intermediate distance of 11 cm should produce an opposite phase. (2) At any distance, the preferred phase at which wing-beat coupling occurs should depend, in part, on the difference in the wing-beat frequencies of the two locusts just before the coupling began. (3) At the moment that the wing-beats of the two locusts become coupled, a change should be observed consistently in the wing-beat frequency of the rear individual only. Each of these three predictions was fulfilled. We also recorded the instantaneous lift of the rear locust by tethering it to a laser torque meter. Lift varied with the phase of the wing-beats between the two locusts. For a given distance between the two locusts, lift was greater by a mean of 16 % of the locust's body mass at those phases where coupling most commonly occurred than at opposite phases. This lift effect was seen even if the wing-beats of the two locusts drifted through these preferred phases without actually coupling. These results are discussed in terms of a possible energetic advantage conferred to the rear locust by flying in tandem and by coupling its flight rhythm to the leader's wing-beat.

Journal Article

The wind-evoked escape behavior of the cricket Gryllus bimaculatus: integration of behavioral elements

The wind-evoked escape behavior of freely ranging crickets (Gryllus bimaculatus) was studied using high-speed video and film analysis. The escape response can be of three types: a turn, a jump or a turn + jump. Any of these can be followed by running. The turn is similar to that of the cockroach, in terms of the details of body and leg movements. A jump occurs only when the cricket has its back to the wind, either because the stimulus came approximately from behind or because the cricket had first turned away from the wind and then jumped. The jump, like that of locust, requires some form of energy storage and quick release to obtain the necessary power. Locusts use long-term co-activation of antagonistic leg motor neurons to produce mechanical energy storage. By contrast, crickets do not appear to co-activate antagonistic leg motor neurons. Possible alternative energy storage and release mechanisms are discussed.

Journal Article