Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 23 December 1966:
Vol. 154. no. 3756, pp. 1515 - 1521
DOI: 10.1126/science.154.3756.1515

Articles

Auditory System of Noctuid Moths

Kenneth D. Roeder 1

1 Department of biology at Tufts University, Medford, Massachusetts; National Academy of Sciences, Washington, D. C.

Insect-eating bats find their aerial food by sonar, through emitting ultrasonic chirps and locating sources of echoes. Certain moths have ears sensitive to these chirps and can detect bats well beyond the range of the bats' sonar. On hearing a distant bat, many moths turn and fly directly away from the source of ultrasound. Only one sense cell in each ear of a moth provides the primary nervous information for this response. This article describes my initial attempts to find out how a moth's central nervous system processes the train of chirps reaching its two ears.

The ear of a restrained moth is exposed to a sequence of artifically generated ultrasonic pulses that approximates the cries made by a bat. This stimulus can be varied with respect to ultrasonic frequency (pitch), pulse intensity, pulse duration, the interval between pulses, and pulse-train duration.

The more sensitive acoustic sense cell responds to all frequencies between about 15,000 and 80,000 cycles per second, but the signal that it transmits to the moth's central nervous system contains no measure of frequency within this range. However, this nerve signal reports variations in the other parameters of the stimulus. The acoustic fiber connects, in the central nervous system, with various nerve cells that transform the signal farther. The signal from a pulse-marker neuron contains no measures of pulse intensity or pulse duration, reporting only changes in interpulse interval and pulse-train duration. A train-marker neuron reports only the duration of the pulse train. The stimulus parameters may be likened to keys, each of which is necessary to gain admittance through a given door but becomes superfluous once this door has been passed. This analogy suggests one of the ways in which a signal is transformed in its passage through the nervous system, and how its specificity is assured in eliciting a given response.

In addition to undergoing this kind of transformation, neural signals generated in the two directionally sensitive ears must be combined if a flying moth is to steer a course away from a distant bat. Neurons have been discovered in the central ganglia which summate signals from the right and left ears. Other neurons are inhibited in their activity by stimulation of one ear. The moth may combine signals from these neurons with motor-nerve information on the attitude of its own wings, which act as oscillating baffles modifying its directional acoustic sensitivity 20 to 40 times a second as it flaps an erratic path through the darkness.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Acoustic feature recognition in the dogbane tiger moth, Cycnia tenera.
J. H. Fullard, J. M. Ratcliffe, and C. G. Christie (2007)
J. Exp. Biol. 210, 2481-2488
   Abstract »    Full Text »    PDF »
'Un chant d'appel amoureux': acoustic communication in moths.
W. Conner (1999)
J. Exp. Biol. 202, 1711-1723
   Abstract »    PDF »
Auditory Sense in Certain Sphingid Moths.
K. D. Roeder, A. E. Treat, and J. S. Vandeberg (1968)
Science 159, 331-333
   Abstract »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)