Skip to main content
Log in

The costs and benefits of frog chorusing behavior

  • Published:
Behavioral Ecology and Sociobiology Aims and scope Submit manuscript

Summary

  1. 1.

    A number of predators, including a bat (Trachops cirrhosus), a frog (Leptodactylus pentadactylus), an opossum (Philander opossum), and a crab (Potamocarcinus richmondi), prey on the neotropical frog Physalaemus pustulosus, which calls in choruses on Barro Colorado Island, Panama.

  2. 2.

    Predation rate (no. of frogs eaten/h of observation) and predation risk to individuals (predation rate/chorus size) were determined for choruses of various sizes. There was no correlation between chorus size and predation rate, but there was a significant negative correlation between chorus size and predation risk.

  3. 3.

    There was a significant correlation between the number of females present and chorus size (i.e., number of males). A second order regression indicates that the proportion of females to males, the operational sex ratio, tends to increase with chorus size; thus, males have a higher probability of mating in larger choruses.

  4. 4.

    We suggest that the benefits of lower predation risk and higher mating probabilities associated with larger choruses were responsible for the evolution of communal sexual display in Physalaemus pustulosus.

  5. 5.

    A cost-benefit model predicts that the size of males that join choruses is influenced by the asymmetric benefits related to male size and the behavior of other males in the population.

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

Access this article

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

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Alexander RD (1975) Natural selection and specialized chorusing behavior in acoustical insects. In: Pimentel D (ed) Insects, science and society. Academic Press, New York, pp 35–77

    Google Scholar 

  • Bell PD (1979) Acoustic attraction of herons by crickets. Entomol Soc 87:126–127

    Google Scholar 

  • Bradbury JW (1981) The evolution of leks. In: Alexander RD, Tinkle DW (eds) Natural selection and social behavior: recent research and new ideas. Chiron Press, New York (in press)

    Google Scholar 

  • Bucher TL, Ryan MJ, Bartholomew, GA (1981) Oxygen consumption during resting, calling, and nest building in the frog. Physalaemus pustulosus. Physiol Zool (in press)

  • Cade W (1975) Acoustically orienting parasitoids: fly phonotaxis to cricket songs. Science 190:1312–1313

    Google Scholar 

  • Cade W (1979) The evolution of alternative male reproductive strategies in field crickets. In: Blum M, Blum N (eds) Sexual selection and reproductive competition in insects. Academic Press, New York, pp 343–380

    Google Scholar 

  • Duellman WE (1958) A monographic study of the colubrid snake genus Leptodiera. Bull Am Mus Nat Hist 114:1–57

    Google Scholar 

  • Emlen ST, Oring LW (1977) Ecology, sexual selection, and the bullfrog. Behav Ecol Sociobiol 1:282–317

    Google Scholar 

  • Emlen ST, Oring IW (1977) Ecology, sexual selection, and the evolution of mating systems. Science 197:215–223

    Google Scholar 

  • Hamilton WD (1971) Geometry for the selfish herd. J Theor Biol 31:295–311

    Google Scholar 

  • Howard RD (1978) The influence of male defended oviposition sites on early embryo mortality in bullfrogs. Ecology 59:789–798

    Google Scholar 

  • Jaeger RG (1976) A possible prey-call window in anuran auditory processing. Copeia 1976:833–834

    Google Scholar 

  • Kluge AG (1981) The life history, social organization, and parental behavior of Hyla rosenbergi Boulenger, a nest building gladiator frog. Occas Pap Mus Zool Univ Mich (in press)

  • Ryan MJ (1980a) Female mate choice in a neotropical frog. Science 209:523–525

    Google Scholar 

  • Ryan MJ (1980b) The reproductive behavior of the bullfrog, Rana catesbeiana. Copeia 1980:108–114

    Google Scholar 

  • Ryan MJ (1981) Variation in iguanine social organizations: mating systems in chuckwallas. In: Burghardt GM, Rand AS (eds) Iguanas of the world: ecology, behavior, conservation. Garland Press, New York (in press)

    Google Scholar 

  • Soper RE, Shewell GE, Tyrell D (1976) Cocandamyia auditrix nov. sp. (Diptera: Scatophagidae), a parasite which is attracted to the call of its host. Can Entomol 108:61–68

    Google Scholar 

  • Tuttle MD, Ryan MJ (1981) The evolution of frog vocalizations in the neotropics. Science (in press)

  • Tuttle MD, Taft LK, Ryan MJ (1980) Location of calling frogs by Philander opossum. Biotropica (in press)

  • Walker TJ (1964) Experimental demonstration of a cat locating orthopteran prey by the prey's call. Fla Entomol 47:163–165

    Google Scholar 

  • Wells KD (1977) The social behaviour of anuran amphibians. Anim Behav 25:666–693

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ryan, M.J., Tuttle, M.D. & Taft, L.K. The costs and benefits of frog chorusing behavior. Behav Ecol Sociobiol 8, 273–278 (1981). https://doi.org/10.1007/BF00299526

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00299526

Keywords

Navigation