Brood parasites lay eggs matching the appearance of host clutches
Jazyk angličtina Země Velká Británie, Anglie Médium electronic-print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24258721
PubMed Central
PMC3843844
DOI
10.1098/rspb.2013.2665
PII: rspb.2013.2665
Knihovny.cz E-zdroje
- Klíčová slova
- brood parasitism, cuckoo, egg coloration, egg mimicry, great reed warbler,
- MeSH
- barva MeSH
- fyziologická adaptace MeSH
- hnízdění * MeSH
- ovum * MeSH
- ptáci fyziologie MeSH
- rozpoznávání (psychologie) MeSH
- vaječná skořápka anatomie a histologie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Interspecific brood parasitism represents a prime example of the coevolutionary arms race where each party has evolved strategies in response to the other. Here, we investigated whether common cuckoos (Cuculus canorus) actively select nests within a host population to match the egg appearance of a particular host clutch. To achieve this goal, we quantified the degree of egg matching using the avian vision modelling approach. Randomization tests revealed that cuckoo eggs in naturally parasitized nests showed lower chromatic contrast to host eggs than those assigned randomly to other nests with egg-laying date similar to naturally parasitized clutches. Moreover, egg matching in terms of chromaticity was better in naturally parasitized nests than it would be in the nests of the nearest active non-parasitized neighbour. However, there was no indication of matching in achromatic spectral characteristics whatsoever. Thus, our results clearly indicate that cuckoos select certain host nests to increase matching of their own eggs with host clutches, but only in chromatic characteristics. Our results suggest that the ability of cuckoos to actively choose host nests based on the eggshell appearance imposes a strong selection pressure on host egg recognition.
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Yoder JB, Nuismer SL. 2010. When does coevolution promote diversification? Am. Nat. 176, 802–817 (doi:10.1086/657048) PubMed DOI
Boulton AM, Polis GA. 2002. Brood parasitism among spiders: interactions between salticids and Diguetia mojavea. Ecology 83, 282–287 (doi:10.2307/2680138) DOI
Cervo R, Macinai V, Dechigi F, Turillazzi S. 2004. Fast growth of immature brood in a social parasite wasp: a convergent evolution between avian and insect cuckoos. Am. Nat. 164, 814–820 (doi:10.1086/425987) PubMed DOI
Sato T. 1986. A brood parasitic catfish of mouthbrooding cichlid fishes in Lake Tanganyika. Nature 323, 58–59 (doi:10.1038/323058a0) PubMed DOI
Davies NB. 2000. Cuckoos, cowbirds and other cheats. London, UK: T & AD Poyser
Rothstein SI. 1990. A model system for coevolution: avian brood parasitism. Annu. Rev. Ecol. Syst. 21, 481–508 (doi:10.1146/annurev.ecolsys.21.1.481) DOI
Feeney WE, Welbergen JA, Langmore NE. 2012. The frontline of avian brood parasite–host coevolution. Anim. Behav. 84, 3–12 (doi:10.1016/j.anbehav.2012.04.011) DOI
Baldamus E. 1853. Neue Beiträge zur Fortpflanzungsgeschichte des europäischen Kuckucks, Cuculus canorus. Naumannia 3, 307–325
Brooke MD, Davies NB. 1988. Egg mimicry by cuckoos Cuculus canorus in relation to discrimination by hosts. Nature 335, 630–632 (doi:10.1038/335630a0) DOI
Gibbs HL, Sorenson MD, Marchetti K, Brooke MD, Davies NB, Nakamura H. 2000. Genetic evidence for female host-specific races of the common cuckoo. Nature 407, 183–186 (doi:10.1038/35025058) PubMed DOI
Fossøy F, Antonov A, Moksnes A, Røskaft E, Vikan JR, Møller AP, Shykoff JA, Stokke BG. 2011. Genetic differentiation among sympatric cuckoo host races: males matter. Proc. R. Soc. B 278, 1639–1645 (doi:10.1098/rspb.2010.2090) PubMed DOI PMC
Moksnes A, Røskaft E. 1995. Egg-morphs and host preference in the common cuckoo (Cuculus canorus): an analysis of cuckoo and host eggs from European museum collections. J. Zool. 236, 625–648 (doi:10.1111/j.1469-7998.1995.tb02736.x) DOI
Starling M, Heinsohn R, Cockburn A, Langmore NE. 2006. Cryptic gentes revealed in pallid cuckoos Cuculus pallidus using reflectance spectrophotometry. Proc. R. Soc. B 273, 1929–1934 (doi:10.1098/rspb.2006.3490) PubMed DOI PMC
Sorenson MD, Payne RB. 2002. Molecular genetic perspectives on avian brood parasitism. Integr. Comp. Biol. 42, 388–400 (doi:10.1093/icb/42.2.388) PubMed DOI
Sorenson MD, Sefc KM, Payne RB. 2003. Speciation by host switch in brood parasitic indigobirds. Nature 424, 928–931 (doi:10.1038/nature01863) PubMed DOI
Clayton DH, Moore J. 1997. Host–parasite evolution: general principles and avian models. Oxford, UK: Oxford University Press
Honza M, Moksnes A, Røskaft E, Stokke BG. 2001. How are different common cuckoo Cuculus canorus egg morphs maintained? An evaluation of different hypotheses. Ardea 89, 341–352
Stoddard MC, Stevens M. 2010. Pattern mimicry of host eggs by the common cuckoo, as seen through a bird's eye. Proc. R. Soc. B 277, 1387–1393 (doi:10.1098/rspb.2009.2018) PubMed DOI PMC
Stoddard MC, Stevens M. 2011. Avian vision and the evolution of egg color mimicry in the common cuckoo. Evolution 65, 2004–2013 (doi:10.1111/j.1558-5646.2011.01262.x) PubMed DOI
Grim T. 2002. Why is mimicry in cuckoo eggs sometimes so poor? J. Avian Biol. 33, 302–305 (doi:10.1034/j.1600-048X.2002.330312.x) DOI
Procházka P, Honza M. 2003. Do common whitethroats (Sylvia communis) discriminate against alien eggs? J. Ornithol. 144, 354–363 (doi:10.1007/bf02465635) DOI
Avilés JM, et al. 2011. The common cuckoo Cuculus canorus is not locally adapted to its reed warbler Acrocephalus scirpaceus host. J. Evol. Biol. 24, 314–325 (doi:10.1111/j.1420-9101.2010.02168.x) PubMed DOI
Avilés JM, Vikan JR, Fossøy F, Antonov A, Moksnes A, Røskaft E, Stokke BG. 2010. Avian colour perception predicts behavioural responses to experimental brood parasitism in chaffinches. J. Evol. Biol. 23, 293–301 (doi:10.1111/j.1420-9101.2009.01898.x) PubMed DOI
Spottiswoode CN, Stevens M. 2010. Visual modelling shows that avian host parents use multiple cues in rejecting parasitic eggs. Proc. Natl Acad. Sci. USA 107, 8672–8676 (doi:10.1073/pnas.0910486107) PubMed DOI PMC
Honza M, Taborsky B, Taborsky M, Teuschl Y, Vogl W, Moksnes A, Røskaft E. 2002. Behaviour of female common cuckoos, Cuculus canorus, in the vicinity of host nests before and during laying: a radiotelemetry study. Anim. Behav. 64, 861–868 (doi:10.1006/anbe.2002.1969) DOI
Wyllie I. 1981. The cuckoo. London, UK: Batsford
Gärtner K. 1981. Das Wegnehmen von Wirtsvogeleiern durch den Kuckuck Cuculus canorus. Ornithologische Mitteilungen 33, 115–131
Moksnes A, Røskaft E, Hagen LG, Honza M, Mork C, Olsen PH. 2000. Common cuckoo Cuculus canorus and host behaviour at reed warbler Acrocephalus scirpaceus nests. Ibis 142, 247–258 (doi:10.1111/j.1474-919X.2000.tb04864.x) DOI
Nakamura H, Miyazawa Y, Kashiwagi K. 2005. Behavior of radio-tracked common cuckoo females during the breeding season in Japan. Ornithol. Sci. 4, 31–41 (doi:10.2326/osj.4.31) DOI
Avilés JM, Stokke BG, Moksnes A, Røskaft E, Åsmul M, Møller AP. 2006. Rapid increase in cuckoo egg matching in a recently parasitized reed warbler population. J. Evol. Biol. 19, 1901–1910 (doi:10.1111/j.1420-9101.2006.01166.x) PubMed DOI
Cherry MI, Bennett ATD, Moskát C. 2007. Do cuckoos choose nests of great reed warblers on the basis of host egg appearance? J. Evol. Biol. 20, 1218–1222 (doi:10.1111/j.1420-9101.2007.01308.x) PubMed DOI
Antonov A, Stokke BG, Fossøy F, Ranke PS, Liang W, Yang CC, Moksnes A, Shykoff J, Røskaft E. 2012. Are cuckoos maximizing egg mimicry by selecting host individuals with better matching egg phenotypes? PLoS ONE 7 e31704 (doi:10.1371/journal.pone.0031704) PubMed DOI PMC
Vorobyev M, Osorio D. 1998. Receptor noise as a determinant of colour thresholds. Proc. R. Soc. Lond. B 265, 351–358 (doi:10.1098/rspb.1998.0302) PubMed DOI PMC
Vorobyev M, Osorio D, Bennett ATD, Marshall NJ, Cuthill IC. 1998. Tetrachromacy, oil droplets and bird plumage colours. J. Comp. Physiol. A Neuroethol. Sens. Neural Behav. Physiol. 183, 621–633 (doi:10.1007/s003590050286) PubMed DOI
Yang CC, et al. 2010. Coevolution in action: disruptive selection on egg colour in an avian brood parasite and its host. PLoS ONE 5, e10816 (doi:10.1371/journal.pone.0010816) PubMed DOI PMC
Gomez D. 2006. AVICOL: a program to analyse spectrometric data, vol. 6 See http://sites.google.com/site/avicolprogram.
Manly BFJ. 1997. Monte Carlo methods. In Randomization, bootstrap, and Monte Carlo methods in biology, pp. 69–78 London, UK: Chapman and Hall
Cassey P, Grim T, Honza M, Hauber ME. 2008. The modelling of avian visual perception model predicts behavioural responses to foreign egg colours. Biol. Lett. 4, 515–517 (doi:10.1098/rsbl.2008.0279) PubMed DOI PMC
Avilés JM. 2008. Egg colour mimicry in the common cuckoo Cuculus canorus as revealed by modelling host retinal function. Proc. R. Soc. B 275, 2345–2352 (doi:10.1098/rspb.2008.0720) PubMed DOI PMC
Avilés JM, Pérez-Contreras T, Navarro C, Soler JJ. 2008. Dark nests and conspicuousness in color patterns of nestlings of altricial birds. Am. Nat. 171, 327–338 (doi:10.1086/527493) PubMed DOI
Osorio D, Vorobyev M. 2005. Photoreceptor spectral sensitivities in terrestrial animals: adaptations for luminance and colour vision. Proc. R. Soc. B 272, 1745–1752 (doi:10.1098/rspb.2005.3156) PubMed DOI PMC
Ödeen A, Håstad O. 2003. Complex distribution of avian color vision systems revealed by sequencing the SWS1 opsin from total DNA. Mol. Biol. Evol. 20, 855–861 (doi:10.1093/molbev/msg108) PubMed DOI
Stoddard MC, Prum RO. 2008. Evolution of avian plumage color in a tetrahedral color space: a phylogenetic analysis of new world buntings. Am. Nat. 171, 755–776 (doi:10.1086/587526) PubMed DOI
Hart NT, Partridge JC, Cuthill IC, Bennett ATD. 2000. Visual pigments, oil droplets, ocular media and cone photoreceptor distribution in two species of passerine bird: the blue tit (Parus caeruelus L.) and the blackbird (Turdus merula L.). J. Comp. Physiol. A Neuroethol. Sens. Neural Behav. Physiol. 186, 375–387 (doi:10.1007/s003590050437) PubMed DOI
Hart NS. 2002. Vision in the peafowl (Aves: Pavo cristatus). J. Exp. Biol. 205, 3925–3935 PubMed
Hart NS. 2001. Variations in cone photoreceptor abundance and the visual ecology of birds. J. Comp. Physiol. A Neuroethol. Sens. Neural Behav. Physiol. 187, 685–697 (doi:10.1007/s00359-001-0240-3) PubMed DOI
Moreno J. 2005. Evidence for the signaling function of egg color in the pied flycatcher Ficedula hypoleuca. Behav. Ecol. 16, 931–937 (doi:10.1093/beheco/ari072) DOI
López de Hierro MDG, De Neve L. 2010. Pigment limitation and female reproductive characteristics influence egg shell spottiness and ground colour variation in the house sparrow (Passer domesticus). J. Ornithol. 151, 833–840 (doi:10.1007/s10336-010-0520-1) DOI
Endler JA, Mielke PW. 2005. Comparing color patterns as birds see them. Biol. J. Linn. Soc. 86, 405–431 (doi:10.1111/j.1095-8312.2005.00540.x) DOI
Maia R, Eliason CHM, Bitton PP, Doucet SM, Shawkey MD. 2013. pavo: an R package for the analysis, visualization and organization of spectral data. Methods Ecol. Evol. 4, 906–913 (doi:10.1111/2041-210X.12069) DOI
R Development Core Team 2012. R: a language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing
Molnár B. 1944. The cuckoo in the Hungarian Plain. Aquila 51, 100–112
Dröscher LM. 1988. A study on radio-tracking of the European cuckoo (Cuculus canorus canorus). Proc. 100th Int. Deutsche Ornithologen-Gesellschaft Meeting. Deutsche Ornithologen-Gesellschaft 187–193
Nakamura H, Miyazawa Y. 1997. Movements, space use and social organisation radio-tracked common cuckoos during the breeding season in Japan. Jpn. J. Ornithol. 46, 23–54 (doi:10.3838/jjo.46.23) DOI
Moskát C, Honza M. 2002. European cuckoo Cuculus canorus parasitism and host's rejection behaviour in a heavily parasitized great reed warbler Acrocephalus arundinaceus population. Ibis 144, 614–622 (doi:10.1046/j.1474-919X.2002.00085.x) DOI
Moskát C, Hauber ME, Avilés JM, Bán M, Hargitai R, Honza M. 2009. Increased host tolerance of multiple cuckoo eggs leads to higher fledging success of the brood parasite. Anim. Behav. 77, 1281–1290 (doi:10.1016/j.anbehav.2009.01.030) DOI
Vogl W, Taborsky M, Taborsky B, Teuschl Y, Honza M. 2002. Cuckoo females preferentially use specific habitats when searching for host nests. Anim. Behav. 64, 843–850 (doi:10.1006/anbe.2002.1967) DOI
Endler JA. 1993. The color of light in forests and its implication. Ecol. Monogr. 63, 1–27 (doi:10.2307/2937121) DOI
Cherry MI, Bennett ATD. 2001. Egg colour matching in an African cuckoo, as revealed by ultraviolet-visible reflectance spectrophotometry. Proc. R. Soc. Lond. B 268, 5565–5571 (doi:10.1098/rspb.2001.2004) PubMed DOI PMC
Honza M, Procházka P, Morongová K, Čapek M, Jelínek V. 2011. Do nest light conditions affect rejection of parasitic eggs? A test of the light environment hypothesis. Ethology 117, 539–546 (doi:10.1111/j.1439-0310.2011.01900.x) DOI
Węgrzyn E, Leniowski K, Rykowska I, Wasiak W. 2011. Is UV and blue-green egg colouration a signal in cavity-nesting birds? Ethol. Ecol. Evol. 23, 121–139 (doi:10.1080/03949370.2011.554882) DOI
Langmore NE, Stevens M, Maurer G, Kilner RM. 2009. Are dark cuckoo eggs cryptic in host nests? Anim. Behav. 78, 461–468 (doi:10.1016/j.anbehav.2009.06.003) DOI
Antonov A, Avilés JM, Stokke BG, Spasova V, Vikan JR, Moksnes A, Yang CC, Liang W, Røskaft E. 2011. Egg discrimination in an open nesting passerine under dim light conditions. Ethology 117, 1128–1137 (doi:10.1111/j.1439-0310.2011.01969.x) DOI
Schaefer HM, Schaefer V, Vorobyev M. 2007. Are fruit colours adapted to consumer vision and birds equally efficient in detecting colourful signals? Am. Nat. 169, S159–S169 (doi:10.1086/510097) PubMed DOI
Moskát C, Szentpéteri J, Barta Z. 2002. Adaptations by great reed warblers to brood parasitism: a comparison of populations in sympatry and allopatry with the common cuckoo. Behaviour 139, 1313–1329 (doi:10.1163/156853902321104181) DOI
Antonov A, Stokke BG, Vikan JR, Fossøy F, Ranke PS, Røskaft E, Moksnes A, Møller AP, Shykoff JA. 2010. Egg phenotype differentiation in sympatric cuckoo Cuculus canorus gentes. J. Evol. Biol. 23, 1170–1182 (doi:10.1111/j.1420-9101.2010.01982.x) PubMed DOI
Honza M, Procházka P, Požgayová M. 2012. Within- and between-season repeatability of eggshell colouration in the great reed warbler Acrocephalus arundinaceus. J. Avian Biol. 43, 91–96 (doi:10.1111/j.1600-048X.2011.05392.x) DOI
Leisler B. 1991. Acrocephalus arundinaceus – Drosselrohrsänger. In Handbuch der Vögel Mitteleuropas, vol. 12, pp. 486–539 Wiesbaden, Germany: Glutz von Blotzheim, UN & Bauer KM
Schulze-Hagen K. 1991. Acrocephalus palustris – Sumpfrohrsänger. In Handbuch der Vögel Mitteleuropas, vol. 12, pp. 377–433 Wiesbaden, Germany: Glutz von Blotzheim UN & Bauer KM
Honkavaara J, Koivula M, Korpimäki E, Siitari H, Viitala J. 2002. Ultraviolet vision and foraging in terrestrial vertebrates. Oikos 98, 505–511 (doi:10.1034/j.1600-0706.2002.980315.x) DOI
Jelínek V, Procházka P, Požgayová M, Honza M. 2013. Common cuckoos Cuculus canorus change their nest-searching strategy according to the number of available host nests. Ibis (doi:10.1111/ibi.12093) DOI
Hart NS, Hunt DM. 2007. Avian visual pigments: characteristics, spectral tuning, and evolution. Am. Nat. 169, S7–S26 (doi:10.1086/510141) PubMed DOI
Mullen P, Pohland G. 2008. Studies on UV reflection in feathers of some 1000 bird species: are UV peaks in feathers correlated with violet-sensitive and ultraviolet-sensitive cones? Ibis 150, 59–68 (doi:10.1111/j.1474-919X.2007.00736.x) DOI
Aidala Z, et al. 2012. Ultraviolet visual sensitivity in three avian lineages: paleognaths, parrots, and passerines. J. Comp. Physiol. A Neuroethol. Sens. Neural Behav. Physiol. 198, 495–510 (doi:10.1007/s00359-012-0724-3) PubMed DOI
Schulze-Hagen K. 1992. Parasitierung und Brutverluste durch Kuckuck (Cuculus canorus) bei Teich- und Sumpfrohrsänger (Acrocephalus scirpaceus, A. palustris) in Mittel- und Westeuropa. J. Ornithol. 133, 237–249 (doi:10.1007/BF01645635) DOI
Lotem A, Nakamura H, Zahavi A. 1992. Rejection of cuckoo eggs in relation to host age: a possible evolutionary equilibrium. Behav. Ecol. 3, 128–132 (doi:10.1093/beheco/3.2.128) DOI
Moskát C, Hauber ME. 2007. Conflict between egg recognition and egg rejection decisions in common cuckoo (Cuculus canorus) hosts. Anim. Cogn. 10, 377–386 (doi:10.1007/s10071-007-0071-x) PubMed DOI
Moskát C, Székely T, Cuthill IC, Kisbenedek T. 2008. Hosts’ response to parasitic eggs: which cues elicit hosts’ egg discrimination? Ethology 114, 186–194 (doi:10.1111/j.1439-0310.2007.01456.x) DOI
Moskát C, Bán M, Székely T, Komdeur J, Lucassen RWG, van Boheemen LA, Hauber ME. 2010. Discordancy or template-based recognition? Dissecting the cognitive basis of the rejection of foreign eggs in hosts of avian brood parasites. J. Exp. Biol. 213, 1976–1983 (doi:10.1242/jeb.040394) PubMed DOI
Soler M, Ruiz-Castellano C, Carra LG, Ontanilla J, Martín-Galvez D. 2013. Do first-time breeding females imprint on their own eggs? Proc. R. Soc. B 280 20122518 (doi:10.1098/rspb.2012.2518) PubMed DOI PMC
Hauber ME, Sherman PW. 2001. Self-referent phenotype matching: theoretical considerations and empirical evidence. Trends Neurosci. 24, 609–616 (doi:10.1016/s0166-2236(00)01916-0) PubMed DOI
Hauber ME, Moskát C, Bán M. 2006. Experimental shift in hosts’ acceptance threshold of inaccurate-mimic brood parasite eggs. Biol. Lett. 2, 177–180 (doi:10.1098/rsbl.2005.0438) PubMed DOI PMC
Bán M, Moskát C, Barta Z, Hauber ME. 2013. Simultaneous viewing of own and parasitic eggs is not required for egg rejection by a cuckoo host. Behav. Ecol. 24, 1014–1021 (doi:10.1093/beheco/art004) DOI
Host genotype and age have no effect on rejection of parasitic eggs