Skip to main content
Log in

Inspection of mob-calls as sources of predator information: response of migrant and resident birds in the Neotropics

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

Abstract

Migrating animals face numerous mortality risks, such as novel predators with which they may not be accustomed. Most animals can recognize predators innately; however, additional predator information can be collected to enhance familiarity. Because migrating birds rarely participate in mobs, they may seek alternative information sources such as cues provided by other birds that can provide information on predator location, identity, and degree of threat. We predicted that Nearctic–Neotropical migrants (hereafter, “migrants”) would react to vocal antipredator cues (e.g., mob-calls) of species residing in areas through which they migrate. To test this, we conducted experiments in Belize during spring migration, using playbacks of mob-calls of black-capped chickadees (Poecile atricapillus) and blue-gray tanagers (Thraupis episcopus); tanagers are familiar to all birds in Belize; chickadees are novel to residents but familiar to migrants. This also allowed us to assess response to novel and out-of-context antipredator signals. Resident birds did not respond to novel chickadee mob-calls, but did respond to familiar tanager calls. Birds overwintering south of our study area, which were migrating during our study, responded most strongly to chickadee playbacks. Conversely, individuals of species that include our study area in their winter range did not respond to either playback. This is the first evidence that birds react to vocal antipredator cues during migration, which may be a strategy used by migrants to learn about predators. Although residents failed to recognize a foreign cue, migrating birds responded most strongly to the out-of-context chickadee cue, associated with breeding grounds >2,000 km northward.

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.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • Belisle M, Desrochers A (2002) Gap-crossing decisions by forest birds: an empirical basis for parameterizing spatially-explicit, individual-based models. Landsc Ecol 17:219–231

    Article  Google Scholar 

  • Betts MG, Hadley AS, Doran PJ (2005) Avian mobbing response is restricted by territory boundaries: experimental evidence from two species of forest warblers. Ethology 111:821–835

    Article  Google Scholar 

  • Boback SM (2005) Natural history and conservation of island boas (Boa constrictor) in Belize. Copeia 4:880–885

    Article  Google Scholar 

  • Brawn JD, Collins TM, Medina M, Bermingham E (1996) Associations between physical isolation and geographical variation within three species of Neotropical birds. Mol Ecol 5:33–46

    Article  Google Scholar 

  • Brown GE (2003) Learning about danger: chemical alarm cues and local risk assessment in prey fishes. Fish Fish 4:227–234

    CAS  Google Scholar 

  • Caro TM (2005) Antipredator defenses in birds and mammals. University of Chicago Press, Chicago

    Google Scholar 

  • Chinchilla FA (1997) Diets of Panthera onca, Felis concolor and Felis pardalis (Carnivora: Felidae) in Parque Nacional Corcovado, Costa Rica. Rev Biol Trop 45:1223–1229

    Google Scholar 

  • Chivers DP, Smith RJF (1994) Fathead minnows, Pimephales promelas, acquire predator recognition when alarm substance is associated with the sight of unfamiliar fish. Anim Behav 48:597–605

    Article  Google Scholar 

  • Conover MR (1987) Acquisition of predator information by active and passive mobbers in ring-billed gull colonies. Behaviour 102:41–57

    Article  Google Scholar 

  • Curio E (1978) The adaptive significance of mobbing. I. Teleonomic hypotheses and predictions. Z Tierpsychol 48:175–183

    Google Scholar 

  • Danchin E, Giraldeau LA, Valone TJ, Wagner RH (2004) Public information: from nosy neighbors to cultural evolution. Science 305:487–491

    Article  PubMed  CAS  Google Scholar 

  • DaSilva JMC, Uhl C, Murray G (1996) Plant succession, landscape management, and the ecology of frugivorous birds in abandoned Amazonian pastures. Conserv Biol 10:491–503

    Article  Google Scholar 

  • Deecke VB, Slater PJB, Ford JKB (2002) Selective habituation shapes acoustic predator recognition in harbour seals. Nature 420:171–173

    Article  PubMed  CAS  Google Scholar 

  • Dierschke V, Delingat J (2001) Stopover behaviour and departure decision of northern wheatears, Oenanthe oenanthe, facing different onward non-stop flight distances. Behav Ecol Sociobiol 50:535–545

    Article  Google Scholar 

  • Dolby AS, Grubb TC (1998) Benefits to satellite members in mixed-species foraging groups: an experimental analysis. Anim Behav 56:501–509

    Article  PubMed  Google Scholar 

  • Drent R, Both C, Green M, Madsen J, Piersma T (2003) Pay-offs and penalties of competing migratory schedules. Oikos 103:274–292

    Article  Google Scholar 

  • Dugatkin LA, Godin JGJ (1992) Prey approaching predators: a cost–benefit perspective. Ann Zool Fenn 29:233–252

    Google Scholar 

  • Edelaar P, Wright J (2006) Potential prey make excellent ornithologists: adaptive, flexible responses towards avian predation threat by Arabian Babblers Turdoides squamiceps living at a migratory hotspot. Ibis 148:664–671

    Article  Google Scholar 

  • Ficken MS, Ficken RW, Witkin SR (1978) Vocal repertoire of the black-capped Chickadee. Auk 95:34–48

    Google Scholar 

  • Fitzgibbon CD (1994) The costs and benefits of predator inspection behavior in Thomson gazelles. Behav Ecol Sociobiol 34:139–148

    Article  Google Scholar 

  • Godin JGJ, Davis SA (1995) Who dares, benefits—predator approach behavior in the guppy (Poecilia reticulata) deters predator pursuit. Proc R Soc Lond B 259:193–200

    Article  Google Scholar 

  • Halupka K, Halupka L (1997) The influence of reproductive season stage on nest defence by meadow pipits (Anthus pratensis). Ethol Ecol Evol 9:89–98

    Google Scholar 

  • Hames RS, Lowe JD, Barker Swarthout S, Rosenberg KV (2006) Understanding the risk to neotropical migrant bird species of multiple human-caused stressors: elucidating processes behind the patterns. Ecol Soc 11, article 24 [online] URL: http://www.ecologyandsociety.org/vol11/iss1/art24/

  • Hilty S (1994) Birds of tropical America. University of Texas Press, Austin

    Google Scholar 

  • Hurd CR (1996) Interspecific attraction to the mobbing calls of black-capped chickadees (Parus atricapillus). Behav Ecol Sociobiol 38:287–292

    Article  Google Scholar 

  • Ishihara M (1987) Effect of mobbing toward predators by the damselfish Pomacentrus coelestis (Pisces, Pomacentridae). J Ethol 5:43–52

    Article  Google Scholar 

  • Jones HL (2003) Birds of Belize. University of Texas Press, Austin

    Google Scholar 

  • Johnson FR, McNaughton EJ, Shelley CD, Blumstein DT (2003) Mechanisms of heterospecific recognition in avian mobbing calls. Aust J Zool 51:577–585

    Article  Google Scholar 

  • Krams I, Krama T (2002) Interspecific reciprocity explains mobbing behaviour of the breeding chaffinches, Fringilla coelebs. Proc R Soc Lond B 269:2345–2350

    Article  Google Scholar 

  • Langham GM, Contreras TA, Sieving KE (2006) Why pishing works: Titmouse (Paridae) scolds elicit a generalized response in bird communities. Ecoscience 13:485–496

    Article  Google Scholar 

  • Latta SC, Wunderle JM (1996) The composition and foraging ecology of mixed-species flocks in pine forests of Hispaniola. Condor 98:595–607

    Article  Google Scholar 

  • Leal M, Rodriguez-Robles JA (1997) Signalling displays during predator–prey interactions in a Puerto Rican anole, Anolis cristatellus. Anim Behav 54:1147–1154

    Article  PubMed  Google Scholar 

  • Lind J, Cresswell W (2005) Determining the fitness consequences of antipredation behavior. Behav Ecol 16:945–956

    Article  Google Scholar 

  • Lind J, Cresswell W (2006) Anti-predation behaviour during bird migration; the benefit of studying multiple behavioural dimensions. J Ornithol 147:310–316

    Article  Google Scholar 

  • Lind J, Jöngren F, Nilsson J, Alm DS, Strandmark A (2005) Information, predation risk and foraging decisions during mobbing in Great Tits Parus major. Ornis Fenn 82:89–96

    Google Scholar 

  • Losito MP, Mirarchi RE, Baldassarre GA (1989) New techniques for time–activity studies of avian flocks in view-restricted habitats. J Field Ornithol 60:388–396

    Google Scholar 

  • Manomet Observatory for Conservation Sciences (1996) Impacts of silvicultural trials on birds and tree regeneration in the Chiquibul Forest Reserve, Belize. Supplement: birds banded and saplings tagged. Report to Ministry of Natural Resources, Belmopan, Belize

  • Marler P (1957) Specific distinctiveness in the communication signals of birds. Behaviour 11:13–39

    Article  Google Scholar 

  • Mathis A, Chivers DP, Smith RJF (1996) Cultural transmission of predator recognition in fishes: intraspecific and interspecific learning. Anim Behav 51:185–201

    Article  Google Scholar 

  • McLean IG, Rhodes G (1991) Enemy recognition and response in birds. Curr Ornithol 8:173–211

    Google Scholar 

  • Mettke-Hofmann C, Gwinner E (2004) Differential assessment of environmental information in a migratory and a nonmigratory passerine. Anim Behav 68:1079–1086

    Article  Google Scholar 

  • Owings DH, Coss RG (1977) Snake mobbing by California ground squirrels—adaptive variation and ontogeny. Behaviour 62:50–69

    Article  Google Scholar 

  • Pijanowska J (1997) Alarm signals in Daphnia? Oecologia 112:12–16

    Article  Google Scholar 

  • Pyle P (1997) Identification guide to North American birds, part 1. Slate Creek, Bolinas

    Google Scholar 

  • R Development Core Team (2006) R: a language environment for statistical computing. R Foundation for Statistical Computing, Vienna

    Google Scholar 

  • Shedd DH (1982) Seasonal variation and function of mobbing and related antipredator behaviors of the American Robin (Turdus migratorius). Auk 99:342–346

    Google Scholar 

  • Sieving KE, Contreras TA, Maute KL (2004) Heterospecific facilitation of forest-boundary crossing by mobbing understory birds in North–Central Florida. Auk 121:738–751

    Article  Google Scholar 

  • Slusarczyk M, Rygielska E (2004) Fish faeces as the primary source of chemical cues inducing fish avoidance diapause in Daphnia magna. Hydrobiologia 526:231–234

    Article  CAS  Google Scholar 

  • Smith SM (1993) Black-capped chickadee (Parus atricapillus). In: Poole A, Gill F (eds) The birds of North America, no 39. The Birds of North America, Philadelphia

    Google Scholar 

  • Srivastava A (1991) Cultural transmission of snake-mobbing in free-ranging Hanuman langurs. Folia Primatol 56:117–120

    Article  PubMed  CAS  Google Scholar 

  • Stutchbury BJM, Morton ES (2001) Behavioral ecology of tropical birds. Academic, London

    Google Scholar 

  • Templeton CN, Greene E (2007) Nuthatches eavesdrop on variations in heterospecific chickadee mobbing alarm calls. Proc Nat Acad Sci 104:5479–5482

    Article  PubMed  CAS  Google Scholar 

  • Templeton CN, Greene E, Davis K (2005) Allometry of alarm calls: black-capped chickadees encode information about predator size. Science 308:1934–1937

    Article  PubMed  CAS  Google Scholar 

  • Tikkanen P, Muotka T, Huhta A (1996) Fishless-stream mayflies express behavioural flexibility in response to predatory fish. Anim Behav 51:1391–1399

    Article  Google Scholar 

  • Turcotte Y, Desrochers A (2002) Playbacks of mobbing calls of black-capped chickadees help estimate the abundance of forest birds in winter. J Field Ornithol 73:303–307

    Google Scholar 

  • Veen T, Richardson DS, Blaakmeer K, Komdeur J (2000) Experimental evidence for innate predator recognition in the Seychelles warbler. Proc R Soc Lond B 267:2253–2258

    Article  CAS  Google Scholar 

  • Winn HE (1960) Biology of the brook stickleback Eucalia inconstans (Kirtland). Am Midl Nat 63:424–438

    Article  Google Scholar 

Download references

Acknowledgment

We are indebted to Trina Fitzgerald (of the Atlantic Bird Observatory) for orchestrating the independent bird-banding studies and commenting on drafts of this manuscript. Two anonymous referees also provided useful comments. Our appreciation is also extended to those who assisted with fieldwork: Kate Dalley, Trina Fitzgerald, Jason Glode, Pete Goulet, and Tina Leonard. We also thank Isidro and Calistro Bol for their field support and station management. Chris Templeton kindly provided recordings of black-capped chickadee calls, while tanager calls were obtained from www.naturesongs.com. The Natural Sciences and Engineering Research Council of Canada (postdoctoral fellowship to JJN, Discovery grants to PDT and LMR), Queen’s University, the National Geographic Society, and the Percy Sladen Memorial Fund supported our research. All field methods used in this research complied with the current laws of Canada and Belize.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Joseph J. Nocera.

Additional information

Communicated by P. Bednekoff

Electronic supplementary material

Below is the link to the electronic supplementary material.

S1

Numbers and migrant status of all migratory bird species captured during passive mist-netting or detected at playbacks black-capped chickadee mob-calls, blue-gray tanager mob-calls, static, or no sound at all in Belize, Central America (DOC 67 KB)

S2

Numbers of all resident bird species captured during passive mist-netting or detected at playbacks black-capped chickadee mob-calls, blue-gray tanager mob-calls, static, or no sound at all in Belize, Central America (DOC 107 KB)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nocera, J.J., Taylor, P.D. & Ratcliffe, L.M. Inspection of mob-calls as sources of predator information: response of migrant and resident birds in the Neotropics. Behav Ecol Sociobiol 62, 1769–1777 (2008). https://doi.org/10.1007/s00265-008-0605-5

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00265-008-0605-5

Keywords

Navigation