Skip to main content
Log in

Hormone-induced vocal behavior and midbrain auditory sensitivity in the green treefrog, Hyla cinerea

  • Published:
Journal of Comparative Physiology A Aims and scope Submit manuscript

Summary

Twenty four castrated male, 6 intact male, and 11 intact female Hyla cinerea were injected subcutaneously with 25 μg arginine-vasotocin (AVT) and induced to call 1 h later in response to the playback of a conspecific mating call. Eighteen castrated males and 8 intact females were implanted 5 mg androgen pellets for 3 weeks prior to the neuropeptide injection. Among castrated males, 6/9 testosterone (T) implanted, 4/9 dihydrotestosterone (DHT) implanted and 2/6 non implanted individuals produced calls after being administered AVT. 5/6 intact non implanted males and 6/8 T intact implanted females also called, and 3 intact non implanted females remained silent after the injection. Evoked calls had a mid-frequency spectral peak at about 1900 Hz which is absent in field-recorded mating calls of this species. Calls of implanted females and castrated non implanted males were shorter than those of castrated implanted and intact non implanted males. Audiograms measured before hormone implants showed dips of enhanced sensitivity at about 0.5, 0.9 and 3.0 kHz in males and females. After AVT injection, thresholds at frequencies within the 0.7–1.5 kHz range were increased in castrated males. Such reduction in sensitivity points to an inhibition of the auditory system during hormone induced vocal activation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

AVT :

arginine-vasotocin

DHT :

dihydrotestosterone

T :

testosterone

TS :

torus semicircularis

References

  • Aitken PG, Capranica RR (1984) Auditory input to a vocal nucleus in the frog Rana pipiens: hormonal and seasonal effects. Exp Brain Res 57:33–39

    Google Scholar 

  • Diakow C, Wilcox JN, Woltmann R (1978) Female frog reproductive behavior elicited in the absence of ovaries. Horm Behav 11:183–189

    Google Scholar 

  • Ewert J-P, Siefert G (1974) Seasonal change of contrast-detection in the toad's (Bufo bufo L.) visual system. J Comp Physiol 94:177–186

    Google Scholar 

  • Gerhardt HC (1974) The significance of some spectral features in mating call recognition in the green treefrog (Hyla cinerea). J Exp Biol 61:229–241

    Google Scholar 

  • Hannigan P, Kelley DB (1985) Androgen-induced alterations in vocalizations of female Xenopus laevis: modifiability and constraints. J Comp Physiol A 158:517–527

    Google Scholar 

  • Hedwig B (1984) Activity and deafness of auditory interneurons during stridulation in the grasshopper Omocestus viridulus (L.) Naturwissenschaften 71:380–381

    Google Scholar 

  • Hillery CM (1984) Seasonality of two midbrain auditory responses in the treefrog, Hyla chrysoscelis. Copeia 1984:844–852

    Google Scholar 

  • Hollander M, Wolfe DA (1973) Nonparametric statistical methods. John Wiley & Sons, New York

    Google Scholar 

  • Keller CH, Zakon HH, Sanchez DV (1986) Evidence for a direct effect of androgens upon electroreceptor tuning. J Comp Physiol A 158:301–310

    Google Scholar 

  • Kelley DB (1980) Auditory vocal nuclei in the frog brain concentrate sex hormones. Science 207:553–555

    Google Scholar 

  • Kelley DB (1986) Neuroeffectors for vocalization in Xenopus laevis: Hormonal regulation of sexual dimorphism. J Neurobiol 17:231–248

    Google Scholar 

  • Kelley DB, Lieberburg I, McEwen BS, Pfaff DW (1978) Autoradiographic and biochemical studies of steroid hormone-concentrating cells in the brain of Rana pipiens. Brain Res 140:287–305

    Google Scholar 

  • Licht P, McCreery BR, Barnes R, Pang R (1983) Seasonal and stress related changes in plasma gonadotropins, sex steroids and corticosterone in the bullfrog, Rana catesbeiana. Gen Comp Endocrinol 50:124–145

    Google Scholar 

  • Littlejohn MJ (1977) Long-range acoustic communication in anurans: An integrated and evolutionary approach. In: Taylor DH, Guttman SI (eds) The reproductive biology of amphibians. Plenum Press, New York, pp 263–294

    Google Scholar 

  • Lombard ER, Straughan IR (1974) Functional aspects of anuran middle ear structures. J Exp Biol 61:71–93

    Google Scholar 

  • McCasland JS, Konishi M (1981) Interaction between auditory and motor activities in an avian song control nucleus. Proc Natl Acad Sci USA 78:7815–7819

    Google Scholar 

  • Moore FL, Miller LJ (1983) Arginine vasotocin induces sexual behavior of newts by acting on cells in the brain, Peptides 4:97–102

    Google Scholar 

  • Moore FL, Zoeller RT (1979) Endocrine control of amphibian seuxal behavior: evidence for a neurohormone-androgen interaction. Horm Behav 13:207–213

    Google Scholar 

  • Moore FL, Zoeller RT, Spielvogel SP, Baum MJ, Han S-J, Crews D, Tokarz RR (1981) Arginine vasotocin enhances influx of testosterone in the newt brain. Comp Biochem Physiol 70:115–117

    Google Scholar 

  • Müller-Preuss P, Ploog D (1981) Inhibition of auditory cortical neurons during phonation. Brain Res 215:61–76

    Google Scholar 

  • Oldham RS, Gerhardt HC (1975) Behavioral isolating mechanisms of the treefrogs Hyla cinerea and Hyla gratiosa. Copeia 1975:223–231

    Google Scholar 

  • Penna M, Capranica RR (1984) Hormonal activation of vocalization and concomitant threshold changes in the central auditory system of the green treefrog. Soc Neurosci Abstr 10:400

    Google Scholar 

  • Pierantoni R, Jela L, Del Rio G, Rastogi RK (1984) Seasonal plasma sex steroid levels in the female Rana esculenta. Gen Comp Endocrinol 53:126–134

    Google Scholar 

  • Sassoon D, Segil N, Kelley D (1986) Androgen-induced myogenesis and chondrogenesis in the larynx of Xenopus laevis. Dev Biol 113:135–145

    Google Scholar 

  • Schafer HJ, Schmidt U (1982) Seasonal changes in retinal function of the frog Rana ridibunda. Behav Process 7:73–79

    Google Scholar 

  • Schmidt RS (1966) Central mechanisms of frog calling. Behaviour 26:251–285

    Google Scholar 

  • Schmidt RS (1980) Development of anuran calling circuits: effect of testosterone propionate injections. Gen Comp Endocrinol 41:80–83

    Google Scholar 

  • Schmidt RS (1982) Masculinization of toad pretrigeminal nucleus by androgens. Brain Res 244:190–192

    Google Scholar 

  • Schmidt RS (1983) Neural correlates of frog calling: masculinization by androgens. Horm Behav 17:94–102

    Google Scholar 

  • Schmidt RS (1984) Mating call phonotaxis in the female American toad: induction by hormones. Gen Comp Endocrinol 55:150–156

    Google Scholar 

  • Segil N, Silverman L, Kelley D, Rainbow (1983) Androgen binding in the laryngeal muscle of Xenopus laevis: sex differences and hormonal regulation. Soc Neurosci Abstr 9:1094

    Google Scholar 

  • Siboulet R (1981) Variations saisonniers de la teneur plasmatique en testosterone et dihydrotestosterone chez le crapaud de Mauritania (Bufo mauritanicus). Gen Comp Endocrinol 45:71–75

    Google Scholar 

  • Siegel S (1956) Nonparametric statistics for the behavioral sciences. McGraw-Hill, New York

    Google Scholar 

  • Specker JL, Moore FL (1980) Annual cycle of plasma androgens and testicular composition in the rough-skinned newt, Taricha granulosa. Gen Comp Endocrinol 42:297–303

    Google Scholar 

  • Suga N, Schlegel P (1973) Neural attenuation of responses to emitted sounds in echolocating bats. Science 177:82–84

    Google Scholar 

  • Wada M, Gorbman A (1977) Relation of mode of administration of testosterone to evocation of male sex behavior in frogs. Horm Behav 8:310–319

    Google Scholar 

  • Walkowiak W (1980) The coding of auditory signals in the torus emicircularis of the fire-bellied toad and the grass frog: responses to simple stimuli and to conspecific calls. J Comp Physiol 138:131–148

    Google Scholar 

  • Wells KD (1977) The social behavior of anurans. Anim Behav 25:666–693

    Google Scholar 

  • Wetzel DM, Kelley DB (1983) Androgen and gonadotropin effects n male mate calls in South African clawed frogs Xenopus laevis. Horm Behav 17:388–404

    Google Scholar 

  • Wilczynski W, Capranica RR (1984) The auditory system of anuran amphibians. Prog Neurobiol 22:1–38

    Google Scholar 

  • Yovanov S, Feng AS (1983) Effects of estradiol on auditory evoked responses from the frog's auditory midbrain. Neurosci Letters 36:291–297

    Google Scholar 

  • Zakon HH, Wilczynski W (1988) The physiology of the anuran eighth nerve. In: Fritzsch B, Ryan MJ, Wilczynski W, Hetherington TE, Walkowiak W (eds) The evolution of the amphibian auditory system. John Wiley & Sons, New York, pp 125–155

    Google Scholar 

  • Zoeller RT, Moore FL (1988) Brain arginine vasotocin concentrations related to sexual behaviors and hydromineral balance in an amphibian. Horm Behav 22:66–75

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Penna, M., Capranica, R.R. & Somers, J. Hormone-induced vocal behavior and midbrain auditory sensitivity in the green treefrog, Hyla cinerea . J Comp Physiol A 170, 73–82 (1992). https://doi.org/10.1007/BF00190402

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00190402

Key words