|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Journal of Experimental Biology, Vol 146, Issue 1 287-306, Copyright © 1989 by Company of Biologists
JOURNAL ARTICLES |
R Hoy, T Nolen and P Brodfuehrer
Section of Neurobiology and Behavior, Cornell University, Ithaca, NY 14853.
The acoustic startle/escape response is a phylogenetically widespread behavioral act, provoked by an intense, unexpected sound. At least six orders of insects have evolved tympanate ears that serve acoustic behavior that ranges from sexual communication to predator detection. Insects that fly at night are vulnerable to predation by insectivorous bats that detect and locate their prey by using biosonar signals. Of the six orders of insects that possess tympanate hearing organs, four contain species that fly at night and, in these, hearing is sensitive to a range of ultrasonic frequencies found in the biosonar signals of bats. Laboratory and field studies have shown that these insects (including some orthopterans, lepidopterans, neuropterans and dictyopterans), when engaged in flight behavior, respond to ultrasound by suddenly altering their flight, showing acoustic startle or negative phonotaxis, which serve as bat-avoidance behavior. A neural analysis of ultrasound-mediated escape behavior was undertaken in the field cricket Telegryllus oceanicus. An identified thoracic interneuron, int-1, was shown to trigger the escape response, but only when the cell was driven (synaptically or electrically) at high spike rates, and only when the insect was performing flight behavior; avoidance steering only occurs in the appropriate behavioral context: flight. Thus, significant constraints operate upon the ability of int-1 to trigger the escape response. The integration of auditory input and flight central pattern generator output occurs in the brain. It is found that neural activity descending from the brain in response to stimulation by ultrasound is increased when the insect is flying compared to when it is not. Although the behavioral act of avoidance steering may appear to be a simple reflex act, further analysis shows it to be anything but simple.
This article has been cited by other articles:
![]() |
R. D. Santer, F. C. Rind, R. Stafford, and P. J. Simmons Role of an Identified Looming-Sensitive Neuron in Triggering a Flying Locust's Escape J Neurophysiol, June 1, 2006; 95(6): 3391 - 3400. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Ratcliffe and J. H. Fullard The adaptive function of tiger moth clicks against echolocating bats: an experimental and synthetic approach J. Exp. Biol., December 15, 2005; 208(24): 4689 - 4698. [Abstract] [Full Text] [PDF] |
||||
![]() |
W Schulze and J Schul Ultrasound avoidance behaviour in the bushcricket Tettigonia viridissima (Orthoptera: Tettigoniidae) J. Exp. Biol., January 2, 2001; 204(4): 733 - 740. [Abstract] [PDF] |
||||
![]() |
P. Faure and R. Hoy Neuroethology of the katydid T-cell. I. Tuning and responses to pure tones J. Exp. Biol., January 11, 2000; 203(21): 3225 - 3242. [Abstract] [PDF] |
||||
![]() |
J. Engel and R. Hoy Experience-dependent modification of ultrasound auditory processing in a cricket escape response J. Exp. Biol., January 10, 1999; 202(20): 2797 - 2806. [Abstract] [PDF] |
||||
![]() |
T Friedel The vibrational startle response of the desert locust Schistocerca gregaria J. Exp. Biol., January 8, 1999; 202(16): 2151 - 2159. [Abstract] [PDF] |
||||
![]() |
D. H. Edwards, S.-R. Yeh, and F. B. Krasne Neuronal coincidence detection by voltage-sensitive electrical synapses PNAS, June 9, 1998; 95(12): 7145 - 7150. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. D. McClellan and A. Hagevik Descending Control of Turning Locomotor Activity in Larval Lamprey: Neurophysiology and Computer Modeling J Neurophysiol, July 1, 1997; 78(1): 214 - 228. [Abstract] [Full Text] [PDF] |
||||