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Voices in the dark: predation risk by owls influences dusk singing in a diurnal passerine

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Abstract

Predation is an important cost of communication in animals and thus a potent selection pressure on the evolution of signaling behavior. Heterospecific eavesdropping by predators may increase the vulnerability of vocalizing prey, particularly during low light, such as at dusk when nocturnal predators are actively hunting. Despite the risk it entails, dawn and dusk chorusing is common in passerines. However, the dusk chorus has not been studied much, neglecting the opportunity for understanding how eavesdropping between predators and prey may shape communication in birds. Here, we report the first demonstration of simulated predation risk (playback of owl vocalizations) altering the dusk chorus of a diurnal passerine, the veery (Catharus fuscescens). Veeries have a pronounced dusk chorus, singing well after sunset and potentially exposing themselves to predation by owls. In response to brief playbacks of owl calls (~30 s of calls presented three times over 25 min), veeries sang fewer songs post-sunset and stopped singing earlier relative to control trials. These changes in singing remained evident 30 min after the last owl stimulus. Although the avian dusk chorus has received relatively little attention to date, our results suggest that the dusk chorus may pose a higher predation risk to singing males that may influence the evolution of singing behavior in diurnal birds.

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References

  • Amrhein V, Kunc HP, Naguib M (2004) Seasonal patterns of singing activity vary with time of day in the nightingale (Luscinia megarhynchos). Auk 121:100–117

    Article  Google Scholar 

  • Andersson M (1994) Sexual selection. Princeton University Press, Princeton

    Google Scholar 

  • Ball M (2000) Vocal behavior of Bicknell’s thrush (Catharus bicknelli). MS thesis, Dalhhousie University, Halifax

  • Balmford A, Thomas ALR, Jones IL (1993) Aerodynamics and the evolution of long tails in birds. Nature 361:628–631

    Article  Google Scholar 

  • Belinsky KL, Hogle JL, Schmidt KA (2012) Veeries experience more acoustic competition at dawn than at dusk. Wilson J Ornithol 124:265–269

    Article  Google Scholar 

  • Berg KS, Brumfield RT, Apanius V (2006) Phylogenetic and ecological determinants of the neotropical dawn chorus. Proc R Soc Lond B 273:999–1005

    Article  CAS  Google Scholar 

  • Campos DP, Bander LA, Raksi A, Blumstein DT (2009) Perch exposure and predation risk: a comparative study in passerines. Acta Ethol 12:93–98

    Article  PubMed  Google Scholar 

  • Catchpole CK, Slater PJB (2008) Bird song: biological themes and variations. Cambridge University Press, Cambridge

    Book  Google Scholar 

  • Deecke VB, Ford JKB, Slater PJB (2005) The vocal behavior of mammal-eating killer whales: communicating with costly calls. Anim Behav 69:395–405

    Article  Google Scholar 

  • Emmering QC, Schmidt KA (2011) Nesting songbirds assess spatial heterogeneity of predatory chipmunks by eavesdropping on their vocalizations. J Anim Ecol 80:1305–1312

    Article  PubMed  Google Scholar 

  • Erne N, Amrhein V (2008) Long-term influence of simulated territorial intrusions on dawn and dusk singing in the winter wren: spring versus autumn. J Ornithol 49:470–486

    Google Scholar 

  • Krams I (2001) Communication in crested tits and the risk of predation. Anim Behav 61:1065–1068

    Article  Google Scholar 

  • La VT (2011) Diurnal and nocturnal birds vocalize at night: a review. Condor 114:245–257

    Google Scholar 

  • Lang AB, Teppner I, Hartbauer M, Romer H (2005) Predation and noise in communication networks of neotropical katydids. In: McGregor P (ed) Animal communication networks. Cambridge University Press, Cambridge, pp 152–169

    Chapter  Google Scholar 

  • Laumann RA, Morales MCB, Cokl A, Borges M (2007) Eavesdropping on sexual vibratory signals of stink bugs (Hemiptera: Pentatomidae) by the egg parasitoid Telenomus podisi. Anim Behav 73:637–649

    Article  Google Scholar 

  • Leopold A, Eynon AE (1961) Avian daybreak and evening song in relation to time and light intensity. Condor 63:269–293

    Article  Google Scholar 

  • Lima SL (2009) Predators and the breeding bird: behavioural and reproductive flexibility under the risk of predation. Biol Rev 84:485–513

    Article  PubMed  Google Scholar 

  • Livezey KB (2007) Barred owl habitat and prey: a review and synthesis of the literature. J Raptor Res 41:177–201

    Article  Google Scholar 

  • Mazur KM, and James PC (2000) Barred owl (Strix varia). In: Poole A, Gill F (eds) The birds of North America, no. 508. The Birds of North America, Inc., Philadelphia, pp 1–24

  • Møller AP, Nielson JT, Garamzegi LZ (2008) Risk-taking by singing males. Behav Ecol 19:41–53

    Article  Google Scholar 

  • Mougeot F, Bretagnolle V (2000) Predation as a cost of sexual communication in nocturnal seabirds: an experimental approach using acoustic signals. Anim Behav 60:647–656

    Article  PubMed  Google Scholar 

  • Nicol JAC, Arnott HJ (1974) Tapeta lucida in the eyes of goatsuckers (Caprimulgidae). Proc R Soc Lond B 187:349–352

    Article  PubMed  CAS  Google Scholar 

  • Otter K, Chruszcz B, Ratcliffe L (1997) Honest advertisement and song output during the dawn chorus of black-capped chickadees. Behav Ecol 8:167–173

    Article  Google Scholar 

  • Peake T (2005) Eavesdropping in communication networks. In: McGregor P (ed) Animal communication networks. Cambridge University Press, Cambridge, pp 13–17

    Chapter  Google Scholar 

  • Poesel A, Kunc HP, Foerter K, Johnsen A, Kempenaers B (2006) Early birds are sexy: male age, dawn song and extra pair paternity in blue tits, Cyanistes (formerly Parus) caeruleus. Anim Behav 72:531–538

    Article  Google Scholar 

  • Rainey HJ, Zuberbühler K, Slater PJB (2004) Hornbills can distinguish between primate alarm calls. Proc R Soc Lond B 271:755–759

    Article  Google Scholar 

  • Randler C (2006) Red squirrels (Sciurus vulgaris) respond to alarm calls of Eurasian jays (Garrulus glandarius). Ethology 112:411–416

    Article  Google Scholar 

  • Roth TC III, Lima SL (2007) The predatory behavior of wintering Accipiter hawks: temporal patterns in activity of predators and prey. Oecologia 152:169–178

    Article  PubMed  Google Scholar 

  • Ryan MJ, Tuttle MD, Taft LJ (1981) The costs and benefits of frog chorusing behavior. Behav Ecol Sociobiol 8:273–278

    Article  Google Scholar 

  • Schmidt KA, Ostfeld RS (2008) Numerical and behavioral effects within a pulse-driven system: consequences for direct and indirect interactions among shared prey. Ecology 89:635–646

    Article  PubMed  Google Scholar 

  • Schmidt KA, Rush SA, Ostfeld RS (2008a) Wood thrush nest success and post-fledging survival across a temporal pulse of small mammal abundance in an oak forest. J Anim Ecol 77:830–837

    Article  PubMed  Google Scholar 

  • Schmidt KA, Lee E, Ostfeld RS, Sieving KS (2008b) Eastern chipmunks increase their perception of predation risk in response to titmouse alarm calls. Behav Ecol 19:759–763

    Article  Google Scholar 

  • Searcy WA, Nowicki S (2008) Bird song and the problem of honest communication. Am Sci 96:114–121

    Article  Google Scholar 

  • Searcy WA, Nowicki S (2005) The evolution of animal communication. Princeton University Press, Princeton

    Google Scholar 

  • Staicer CA, Spector DA, Horn AG (1996) Diel patterns in acoustic signalling. In: Kroodsma DE, Miller EH (eds) Ecology and evolution of acoustic communication in birds. Cornell University Press, Ithaca, pp 426–453

    Google Scholar 

  • Streby HM, Refsnider JM, Peterson SM, Andersen DE (2008) Barred owl predation on hermit thrush and ovenbird fledglings. J Raptor Res 42:296–298

    Article  Google Scholar 

  • Thomas RJ, Szekely T, Cuthill IC, Harper DGC, Newson SE, Frayling TD, Wallis PD (2002) Eye size in birds and the timing of song at dawn. Proc R Soc Lond B 269:831–837

    Article  Google Scholar 

  • Werner EE, Anholt BR (1993) Ecological consequences of the tradeoff between growth and mortality rates mediated by foraging activity. Am Nat 142:242–272

    Article  PubMed  CAS  Google Scholar 

  • Woods CP, Brigham RM (2008) Common poorwill activity and calling behavior in relation to moonlight and predation. Wil J Ornith 120:505–512

    Article  Google Scholar 

  • Zahavi A (1975) Mate selection—a selection for a handicap. J Theor Biol 53:205–214

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

The authors thank Stacy Tekstar, Angela Olsen, and Claire Randall for patiently and meticulously identifying all of the veery songs throughout these long recordings, and Janice Kelly for additional support in the field. Two anonymous reviewers provided constructive comments to an earlier draft of the manuscript. This research was supported in part by a grant to KAS from the National Science Foundation (DEB 0746985).

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Our study was conducted in compliance with the ethical standards of animal care and use at Texas Tech University and the United States of America.

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Correspondence to Kenneth A. Schmidt.

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Communicated by M. Hughes

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Schmidt, K.A., Belinsky, K.L. Voices in the dark: predation risk by owls influences dusk singing in a diurnal passerine. Behav Ecol Sociobiol 67, 1837–1843 (2013). https://doi.org/10.1007/s00265-013-1593-7

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  • DOI: https://doi.org/10.1007/s00265-013-1593-7

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