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Physiological characteristics of the tympanic organ in noctuoid moths

III. Post-stimulus phenomena

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Summary

We show the variations in the spike activity of both auditory receptors inSpodoptera frugiperda, Mocis latipes, Ascalapha odorata (Noctuidae),Maenas jussiae andEmpyreuma pugione (Arctiidae) immediately after 45 ms and 5 s acoustic stimuli at different intensities. The frequency of the applied stimuli was 34 kHz forE. pugione and 20 kHz for the other species. The electrical activity of the auditory receptors was recorded at the tympanic nerve with a stainless steel hook electrode. When the 45 ms pulses cease there is an afterdischarge from both auditory receptors in all the species. The number of spikes in the afterdischarge activity of both receptor cells (A1 and A2) shows a linear relation with stimulus intensity (Table 1). This number increases monotonically with increments in stimulus intensity, except for the A1 cell activity inE. pugione, which decreases at intensities higher than 55 dB (Fig. 1). There are significant species-specific differences in the slope values of the number of spikes in the afterdischarge of both auditory receptors. After a 5 s stimulusM. latipes andM. jussiae show a rapid recovery of the standard spontaneous A1-cell discharge level. Poststimulus A1-cell spike activity inS. frugiperda shows a silent period, the duration of which increases with stimulus intensity (Fig. 3).E. pugione andA. odorata show such a silent period after low and moderately intense stimuli, but at high intensities the post-stimulus activity exceeds the pre-stimulus spontaneous discharge (Fig. 3). We demonstrate statistically that these variations cannot be explained by the random fluctuations of the standard spontaneous discharge. They are thus considered a silent and a rebound period respectively (Fig. 5). The presence and duration of either type of period seem to depend on the magnitude of the response to the acoustic stimulus. They thus seem related to the adaptation rate and the previously suggested existence of peripheral inhibitory interaction between the auditory receptors.

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References

  • Adams WB (1971) Intensity characteristics of the noctuid acoustic receptor. J Gen Physio) 58:562–579

    Google Scholar 

  • Coro F (1979) Organizatión morfo-funcional de los receptores auditivos enEmpyreuma pugione (Lepidoptera). PhD thesis La Habana-Moscow

  • Coro F, Pérez M (1983) Peripheral interaction in the tympanic organ of a moth. Naturwissenschaften 70:99–100

    Google Scholar 

  • Coro F, Pérez M (1984) Intensity coding by auditory receptors inEmpyreuma pugione (Lepidoptera, Ctenuchidae). J Comp Physiol A 154:287–295

    Google Scholar 

  • Coro F, Pérez M, López JR (1984) Emisión de señales acústicas enEmpyreuma pugione (Lepidoptera, Ctenuchidae). Cien Biol 10:5–18

    Google Scholar 

  • Eggers F (1916) Notes supplementaires sur l'organe tympanal thoracal des Noctuides et de quelques autres familles de Lepidoptères. Rev Russe d'Entomol 16:249–265

    Google Scholar 

  • Eggers F (1919) Das thoracale bitympanale Organ einer Gruppe der Lepidoptera Heterocera. Zool Jb (Anat) 41:273–376

    Google Scholar 

  • Fullard JH (1982) Cephalic influences on a defensive behavior in the dogbane tiger moth,Cycnia tenera. Physiol Entomol 7:157–162

    Google Scholar 

  • Ghiradella H (1971) Fine structure of the noctuid moth ear. I. The transducer area and connection to the tympanic membrane inFeltia subgothica (Haworth). J Morphol 134:21–45

    Google Scholar 

  • Hartline HK, Ratliff F, Miller WH (1961) Inhibitory interaction in the retina and its significance in vision. In: Florey E (ed) Nervous inhibition. Pergamon Press, London, pp 241–284

    Google Scholar 

  • Haskell PT, Beiton P (1956) Electrical responses in certain lepidopterous tympanic organs. Nature 177:139–140

    Google Scholar 

  • Kay RE (1969) Acoustic signalling and its possible relationship to assembling and navigation in the moth,Heliothis zea. J Insect Physiol 15:989–1001

    Google Scholar 

  • Lechtenberg R (1971) Acoustic response of the B cell in noctuid moths. J Insect Physiol 17:2395–2408

    Google Scholar 

  • Miller LA (1982) The orientation and evasive behavior of insects to bat cries. In: Addink AD, Spronk N (eds) Exogenous and endogenous influences on metabolism and neural control. Vol I. Pergamon Press, London, pp 393–405

    Google Scholar 

  • Neuweiler G (1983) Echolocation. In: Hoppe W, Lohmann W, Markl H, Ziegler H (eds) Biophysics. Springer, Berlin Heidelberg New York, pp 683–697

    Google Scholar 

  • Neuweiler G (1984) Foraging, echolocation and audition in bats. Naturwissenschaften 71:446–455

    Google Scholar 

  • Pérez M, Coro F (1983) Activitdad eléctrica espontánea del órgano timpánico en varias especies de lepidópteros. Cien Biol 9:25–36

    Google Scholar 

  • Pérez M, Coro F (1984) Physiological characteristics of the tympanic organ in noctuoid moths. I. Responses to brief acoustic pulses. J Comp Physiol A 154:441–447

    Google Scholar 

  • Pérez M, Coro F (1985) Physiological characteristics of the tympanic organ in noctuoid moths. II. Responses to 45 ms and 5 s acoustic stimuli. J Comp Physiol A 156:689–696

    Google Scholar 

  • Ratliff F (1961) Inhibitory interaction and the detection and enhancement of contours. In: Rosenblith WA (ed) Sensory communication. Technology Press, Cambridge, pp 325–340

    Google Scholar 

  • Roeder KD (1964a) Aspects of the noctuid tympanic nerve response having significance in the avoidance of bats. J Insect Physiol 10:529–546

    Google Scholar 

  • Roeder KD (1964b) Night fighters in a sonic duel. Natural History 73:33–39

    Google Scholar 

  • Roeder KD (1974a) Responses of the less sensitive acoustic sense cells in the tympanic organs of some noctuid and geometrid moths. J Insect Physiol 20:55–66

    Google Scholar 

  • Roeder KD (1974b) Acoustic sensory responses and possible bat evasion tactics of certain moths. Can Soc Zool Annu Meeting, Proc Univ New Brunswick, Fredricton, pp 71–78

    Google Scholar 

  • Roeder KD, Treat AE (1957) Ultrasonic reception by the tympanic organ of noctuid moths. J Exp Zool 134:127–158

    Google Scholar 

  • Roeder KD, Treat AE (1960) The acoustic detection of bats by moths. Proc XI Intern Entomol Congr, pp 150–158

  • Schiolten P, Larsen ON, Michelsen A (1981) Mechanical time resolution in some insect ears. I. Impulse responses and time constants. J Comp Physiol 143:289–295

    Google Scholar 

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Pérez, M., Coro, F. Physiological characteristics of the tympanic organ in noctuoid moths. J. Comp. Physiol. 159, 115–122 (1986). https://doi.org/10.1007/BF00612502

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