• Barber J R
• Conner W E

The Journal of experimental biology

• Publish Date: Jul 2006
• ISSN: 0022-0949
• Volume: 209
• Issue: Pt 14
• Pages: 2637-50
• Medium: Print
• Language: English
• Citation (JAMA): Barber J R, Conner W E, et al. Tiger Moth Responses to a Simulated Bat Attack: Timing and Duty Cycle.. J. Exp. Biol. Jul 2006;209:2637-50

Abstract

Many night-flying insects perform complex, aerobatic escape maneuvers when echolocating bats initiate attack. Tiger moths couple this kinematic defense with an acoustic reply to a bat’s biosonar-guided assault. The jamming hypothesis for the function of these moth sounds assumes that tiger moth clicks presented at high densities, temporally locked to the terminal phase of the bat attack will produce the greatest jamming efficacy. Concomitantly, this hypothesis argues that moths warning bats of bad tasting chemicals sequestered in their tissues should call early to give the bat time to process the meaning of the warning signal and that moths calling at low duty cycles are more likely to employ such an aposematic strategy. We report here the first investigation of a tiger moth assemblage’s response to playback of a bat echolocation attack sequence. This assemblage of arctiid moths first answered the echolocation attack sequence 960+/-547 ms (mean +/- s.d.) from the end of the bat attack. The assemblage reached a half-maximum response shortly after the first response, at 763+/-479 ms from the end of the terminal buzz. Tiger moth response reached a maximum at 475+/-344 ms from the end of the sequence; during the approach phase, well before the onset of the terminal buzz. In short, much of tiger moth response to bat attack occurs outside of the jamming hypotheses’ predictions. Furthermore, no relationship exists between the duty cycle of a tiger moth’s call (and thus the call’s probability of jamming the bat) and its temporal response to bat attack. These data call into doubt the assumptions behind the jamming hypothesis as currently stated but do not directly test the functionality of arctiid sounds in disrupting echolocation in bat-moth aerial battles.

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