Organisms can minimize their exposure to risk of death or injury by assessing their environment and modifying their behavior accordingly. There is evidence that the current or recent presence of a predator introduces cues to the environment that organisms may use in risk assessment. However, we know little about whether terrestrial organisms use the remains of victims of predation as one such cue of elevated predation risk. A previous study showed that western scrub-jays (Aphelocoma californica) respond both to dead conspecifics and to encounters with a predator with alarm calling and aggregation (cacophonous aggregations), suggesting that they use dead conspecifics as indirect evidence of predation risk. Here we examine whether western scrub-jays also use dead heterospecifics as an indicator of risk. We find that jays respond with cacophonous aggregations to dead sympatric and allopatric jay-size heterospecifics but react weakly if at all to smaller heterospecifics. This suggests that size may be an important factor in determining whether a dead heterospecific is a relevant cue of risk. To our knowledge this is the first controlled experiment showing an animal using the visual cue provided by a dead heterospecific as an indicator of risk and communicating this risk to other conspecifics.
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Abbott K.R. (2006). Bumblebees avoid flowers containing evidence of past predation events. — Can. J. Zool. 84: 1240-1247.
Anderson D.R. (2008). Model based inference in the life sciences: a primer on evidence, 2nd edn. — Springer, Berlin.
Anderson J.R., Gillies A., Lock L.C. (2010). Pan thanatology. — Curr. Biol. 20: R349-R351.
Andersson M., Norberg R.A. (1981). Evolution of reversed sexual size dimorphism and role partitioning among predatory birds, with a size scaling of flight performance. — Biol. J. Linn. Soc. 15: 105-130.
Apfelbach R., Blanchard C.D., Blanchard R.J., Hayes R.A., McGregor I.S. (2005). The effects of predator odors in mammalian prey species: a review of field and laboratory studies. — Neurosci. Biobehav. Rev. 29: 1123-1144.
Barash D.P. (1976). Mobbing behavior by crows: the effects of the ‘crow-in-distress’ model. — Condor 78: 120.
Barrera J.P., Chong L., Judy K.N., Blumstein D.T. (2011). Reliability of public information: predators provide more information about risk than conspecifics. — Anim. Behav. 81: 779-787.
Bielefeldt J., Rosenfield R.N., Stout W.E., Vos S.M. (1998). The cooper’s hawk in wisconsin: a review of its breeding biology and status. — Passenger Pigeon 60: 111-121.
Bonnaud E., Medina F.M., Vidal E., Nogales M., Tershy B., Zavaleta E., Donlan C.J., Keitt B., Le Corre M., Horwath S.V. (2011). The diet of feral cats on islands: a review and a call for more studies. — Biol. Invas. 13: 581-603.
Carmen W.J. (2004). Noncooperative breeding in the Californian scrub-jay, Studies in avian biology, Vol. 28. — Cooper Ornithological Society, Camarillo, CA.
Chivers D.P., Kiesecker J.M., Wildy E.L., Anderson M.T., Blaustein A.R. (1997). Chemical alarm signalling in terrestrial salamanders: intra- and interspecific responses. — Ethology 103: 599-613.
Chivers D.P., Kiesecker J.M., Wildy E.L., Belden L.K., Kats L.B., Blaustein A.R. (1999). Avoidance response of post-metamorphic anurans to cues of injured conspecifics and predators. — J. Herpetol. 33: 472-476.
Chivers D.P., Mirza R.S., Johnston J.G. (2002). Learned recognition of heterospecific alarm cues enhances survival during encounters with predators. — Behaviour 139: 929-938.
Chivers D.P., Smith R.J.F. (1998). Chemical alarm signalling in aquatic predator-prey systems: a review and prospectus. — Ecoscience 5: 338-352.
Cooper W.E. Jr. (2008). Visual monitoring of predators: occurrence, cost and benefit for escape. — Anim. Behav. 76: 1365-1372.
Curio E. (1978). Adaptive significance of avian mobbing. 1. Teleonomic hypotheses and predictions. — Z. Tierpsychol. 48: 175-183.
Ellis J.M.S. (2008). Which call parameters signal threat to conspecifics in white-throated magpie-jay mobbing calls? — Ethology 114: 154-163.
Evans C.S., Evans L., Marler P. (1993). On the meaning of alarm calls: functional reference in an avian vocal system. — Anim. Behav. 46: 23-38.
Fallow P.M., Magrath R.D. (2010). Eavesdropping on other species: mutual interspecific understanding of urgency information in avian alarm calls. — Anim. Behav. 79: 411-417.
Flasskamp A. (1994). The adaptive significance of avian mobbing V: an experimental test of the ‘move on’ hypothesis. — Ethology 96: 322-333.
Golightly R.T., Faulhaber M.R., Sallee K.L., Lewis J.C. (1994). Food habits and management of introduced red fox in Southern California. — In: Proceedings of the Sixteenth Vertebrate Pest Conference, Santa Clara, CA, 28 February–3 March 1994, p. 15-20.
Gotmark F., Post P. (1996). Prey selection by sparrowhawks, accipiter nisus: relative predation risk for breeding passerine birds in relation to their size, ecology and behaviour. — Phil. Trans. Roy. Soc. Lond. Ser. B: Biol. Sci. 351: 1559-1577.
Griesser M. (2008). Referential calls signal predator behavior in a group-living bird species. — Curr. Biol. 18: 69-73.
Griesser M. (2009). Mobbing calls signal predator category in a kin group-living bird species. — Proc. Roy. Soc. Lond. B: Biol. Sci. 276: 2887-2892.
Griffin A.S. (2004). Social learning about predators: a review and prospectus. — Learn. Behav. 32: 131-140.
Griffin A.S., Boyce H.M., MacFarlane G.R. (2010). Social learning about places: observers may need to detect both social alarm and its cause to learn. — Anim. Behav. 79: 459-465.
Hamilton W.D. (1971). Geometry for the selfish herd. — J. Theor. Biol. 31: 295-311.
Heinrich B. (1999). Mind of the raven: investigations and adventures with wolf-birds. — Cliff Street Books, New York, NY.
Hernandez L., Laundre J.W. (2005). Foraging in the ‘landscape of fear’ and its implications for habitat use and diet quality of Elk cervus elaphus and Bison bison bison. — Wildlife Biol. 11: 215-220.
Hockman J.G., Chapman J.A. (1983). Comparative feeding habits of red foxes (Vulpes vulpes) and gray foxes (Urocyon cinereoargenteus) in Maryland. — Am. Midl. Nat. 110: 276-285.
Howland H.C. (1974). Optimal strategies for predator avoidance: the relative importance of speed and manoeuvrability. — J. Theor. Biol. 47: 333-350.
Iglesias T.L., McElreath R., Patricelli G.L. (2012). Western scrub-jay funerals: cacophonous aggregations in response to dead conspecifics. — Anim. Behav. 84: 1103-1111.
Johnson J.B., Omland K.S. (2004). Model selection in ecology and evolution. — Trends Ecol. Evol. 19: 101-108.
Kats L.B., Dill L.M. (1998). The scent of death: chemosensory assessment of predation risk by prey animals. — Ecoscience 5: 361-394.
Kruuk H. (1976). The biological function of gulls’ attraction towards predators. — Anim. Behav. 24: 146-153.
Laundre J.W., Hernandez L., Altendorf K.B. (2001). Wolves, elk, and bison: reestablishing the “landscape of fear” in Yellowstone National Park, USA. — Can. J. Zool. 79: 1401-1409.
Lima S.L., Dill L.M. (1990). Behavioral decisions made under the risk of predation — a review and prospectus. — Can. J. Zool. 68: 619-640.
Magrath R.D., Bennett T.H. (2012). A micro-geography of fear: learning to eavesdrop on alarm calls of neighbouring heterospecifics. — Proc. Roy. Soc. Lond. B: Biol. Sci. 279: 902-909.
Magrath R.D., Pitcher B.J., Gardner J.L. (2009). Recognition of other species’ aerial alarm calls: speaking the same language or learning another? — Proc. Roy. Soc. Lond. B: Biol. Sci. 276: 769-774.
Manzur T., Navarrete S.A. (2011). Scales of detection and escape of the sea urchin tetrapygus niger in interactions with the predatory sun star heliaster helianthus. — J. Exp. Mar. Biol. Ecol. 407: 302-308.
Marzluff J.M., Angell T. (2007). In the company of crows and ravens. — Yale University Press, New Haven, CT.
McComb K., Baker L., Moss C. (2006). African elephants show high levels of interest in the skulls and ivory of their own species. — Biol. Lett. 2: 26-28.
Miller W.R., Brigham R.M. (1988). “Ceremonial” gathering of black-billed magpies (Pica pica) after the sudden death of a conspecific. — Murrelet 69: 78-79.
Mirza R.S., Chivers D.P. (2003). Fathead minnows learn to recognize heterospecific alarm cues they detect in the diet of a known predator. — Behaviour 140: 1359-1369.
Pearre S., Maass R. (1998). Trends in the prey size-based trophic niches of feral and house cats Felis catus L. — Mamm. Rev. 28: 125-139.
Poole A. (2007). The birds of North American online. — Cornell Laboratory of Ornithology, Ithaca, NY, available online at: http://bna.birds.cornell.edu/bna.
Ramakrishnan U., Coss R.G. (2000). Recognition of heterospecific alarm vocalizations by bonnet macaques (Macaca radiata). — J. Comp. Psychol. 114: 3-12.
Richards D.B., Thompson N.S. (1978). Critical properties of assembly call of common American crow. — Behaviour 64: 184-203.
Robinson S.K. (1985). Coloniality in the yellow-rumped cacique as a defense against nest predators. — Auk 102: 506-519.
Roth T.C., Lima S.L. (2003). Hunting behavior and diet of cooper’s hawks: an urban view of the small-bird-in-winter paradigm. — Condor 105: 474-483.
Seyfarth R.M., Cheney D.L., Marler P. (1980). Vervet monkey alarm calls: semantic communication in a free-ranging primate. — Anim. Behav. 28: 1070-1094.
Shier D.M., Owings D.H. (2007). Effects of social learning on predator training and postrelease survival in juvenile black-tailed prairie dogs, Cynomys ludovicianus. — Anim. Behav. 73: 567-577.
Shrader A.M., Brown J.S., Kerley G.I.H., Kotler B.P. (2008). Do free-ranging domestic goats show ‘landscapes of fear’? Patch use in response to habitat features and predator cues. — J. Arid Environm. 72: 1811-1819.
Templeton C.N., Greene E. (2007). Nuthatches eavesdrop on variations in heterospecific chickadee mobbing alarm calls. — Proc. Natl. Acad. Sci. USA 104: 5479-5482.
Templeton C.N., Greene E., Davis K. (2005). Allometry of alarm calls: black-capped chickadees encode information about predator size. — Science 308: 1934-1937.
Verheggen F.J., Haubruge E., Mescher M.C. (2010). Alarm pheromones — chemical signaling in response to danger. — Vitamins Hormones 83: 215-239.
Warkentin K.M. (2005). How do embryos assess risk? Vibrational cues in predator-induced hatching of red-eyed treefrogs. — Anim. Behav. 70: 59-71.
Webber T. (1984). Form and function of the long-range calls of scrub jays, Aphelocoma coerulescens obscura. — Unpublished PhD Dissertation, University of Florida, Gainesville, FL.
Wisenden B.D. (2000). Olfactory assessment of predation risk in the aquatic environment. — Phil. Trans. R. Soc. Lond. Ser. B: Biol. Sci. 355: 1205-1208.
Yorzinski J.L., Vehrencamp S.L. (2009). The effect of predator type and danger level on the mob calls of the american crow. — Condor 111: 159-168.
Zuberbühler K. (2000). Referential labelling in Diana monkeys. — Anim. Behav. 59: 917-927.
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Organisms can minimize their exposure to risk of death or injury by assessing their environment and modifying their behavior accordingly. There is evidence that the current or recent presence of a predator introduces cues to the environment that organisms may use in risk assessment. However, we know little about whether terrestrial organisms use the remains of victims of predation as one such cue of elevated predation risk. A previous study showed that western scrub-jays (Aphelocoma californica) respond both to dead conspecifics and to encounters with a predator with alarm calling and aggregation (cacophonous aggregations), suggesting that they use dead conspecifics as indirect evidence of predation risk. Here we examine whether western scrub-jays also use dead heterospecifics as an indicator of risk. We find that jays respond with cacophonous aggregations to dead sympatric and allopatric jay-size heterospecifics but react weakly if at all to smaller heterospecifics. This suggests that size may be an important factor in determining whether a dead heterospecific is a relevant cue of risk. To our knowledge this is the first controlled experiment showing an animal using the visual cue provided by a dead heterospecific as an indicator of risk and communicating this risk to other conspecifics.
All Time | Past Year | Past 30 Days | |
---|---|---|---|
Abstract Views | 436 | 95 | 1 |
Full Text Views | 196 | 21 | 0 |
PDF Views & Downloads | 112 | 43 | 0 |