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Phenotypic Plasticity in Egg Rejection: Evidence and Evolutionary Consequences

  • Francisco Ruiz-Raya
  • Manuel Soler
Chapter
Part of the Fascinating Life Sciences book series (FLS)

Abstract

Rejection of parasitic eggs is the most common and effective defence used by hosts to mitigate the fitness costs imposed by avian brood parasites. Although egg rejection importantly relies on the cognitive abilities of parasitized individuals, both theoretical models and experimental studies have found that some hosts are able to modify their response according to the current conditions of parasitism, which reflects the existence of phenotypic plasticity in host defences. In environments in which the risk of parasitism is variable, plastic responses can be favoured by natural selection as they will allow hosts to avoid potential rejection costs under low risk of parasitism. In this chapter, we review the current evidence of plastic responses in egg rejection and discuss both the evolution and the long-term consequences of phenotypic plasticity for brood parasite–host coevolution. In addition, we suggest addressing the study of egg rejection as a complex process affected by multiple components and governed by decision-making and host motivation, which has important implications for host responses. Despite its apparent benefits, phenotypic plasticity is scarce among host species. Thus, the evolution of phenotypic plasticity in brood parasite–host systems deserves special attention as the maintenance or the loss of plastic responses involves important evolutionary consequences, affecting the long-term outcome of the interaction between brood parasites and their hosts. We conclude this chapter with some suggestions to deal with phenotypic plasticity in future egg-rejection studies.

Keywords

Egg-rejection process Environmental heterogeneity Decision-making Egg recognition Flexible defences Motivation Risk of parasitism Rejection costs 

Notes

Acknowledgements

We greatly thank Naomi Langmore and Brian Peer, who provided useful comments which significantly improved this chapter.

References

  1. Agrawal AA (2001) Phenotypic plasticity in the interactions and evolution of species. Science 294:321–326PubMedCrossRefGoogle Scholar
  2. Álvarez F (1996) Model cuckoo Cuculus canorus eggs accepted by rufous bush chats Cercotrichas galactotes during the parasite’s absence from the breeding area. Ibis 138:340–342CrossRefGoogle Scholar
  3. Antonov A, Stokke BG, Moksnes A, Røskaft E (2009) Evidence for egg discrimination preceding failed rejection attempts in a small cuckoo host. Biol Lett 5:169–171CrossRefPubMedGoogle Scholar
  4. Baglione V, Bolopo D, Canestrari D, Martínez JG, Roldán M, Vila M, Soler M (2017) Spatiotemporal variation of host use in a brood parasite: the role of the environment. Behav Ecol 28:49–58CrossRefGoogle Scholar
  5. Bartol I, Karcza Z, Moskát C, Røskaft E, Kisbenedek T (2002) Responses of great reed warblers Acrocephalus arundinaceus to experimental brood parasitism: the effects of a cuckoo Cuculus canorus dummy and egg mimicry. J Avian Biol 33:420–425CrossRefGoogle Scholar
  6. Briskie JV, Sealy SG, Hobso KA (1992) Behavioral defenses against avian brood parasitism in sympatric and allopatric host populations. Evolution 46:334–340CrossRefPubMedGoogle Scholar
  7. Britton NF, Planqué R, Franks NR (2007) Evolution of defence portfolios in exploiter-victim systems. Bull Math Biol 69:957–988PubMedPubMedCentralCrossRefGoogle Scholar
  8. Brooke MDL, Davies NB (1988) Egg mimicry by cuckoos Cuculus canorus in relation to discrimination by hosts. Nature 335:630–632CrossRefGoogle Scholar
  9. Brooke MDL, Davies NB, Noble DG (1998) Rapid decline of host defences in response to reduced cuckoo parasitism: behavioural flexibility of reed warblers in a changing world. Proc R Soc B 265:1277–1282CrossRefGoogle Scholar
  10. Brooker LC, Brooker MG, Brooker AMH (1990) An alternative population/genetics model for the evolution of egg mimesis and egg crypsis in cuckoos. J Theor Biol 146:123–143CrossRefGoogle Scholar
  11. Burgham MCJ, Picman J (1989) Effect of brown-headed cowbirds on the evolution of yellow warbler anti-parasite strategies. Anim Behav 38:298–308CrossRefGoogle Scholar
  12. Campobello D, Sealy SG (2011) Use of social over personal information enhances nest defense against avian brood parasitism. Behav Ecol 22:422–428CrossRefGoogle Scholar
  13. Chakra MA, Hilbe C, Traulsen A (2014) Plastic behaviors in hosts promote the emergence of retaliatory parasites. Sci Rep 4:4251.  https://doi.org/10.1038/srep04251 CrossRefPubMedPubMedCentralGoogle Scholar
  14. Cruz A, Prather JW, Wiley JW, Weaver PF (2008) Egg rejection behavior in a population exposed to parasitism: village weavers on Hispaniola. Behav Ecol 19:398–403CrossRefGoogle Scholar
  15. Davies NB (2000) Cuckoos, cowbirds and other cheats. T. & A. D. Poyser, LondonGoogle Scholar
  16. Davies NB, Brooke MDL (1988) Cuckoos versus reed warblers: adaptations and counteradaptations. Anim Behav 36:262–284CrossRefGoogle Scholar
  17. Davies NB, Brooke MDL (1989) An experimental study of co-evolution between the cuckoo, Cuculus canorus, and its hosts. I. Host egg discrimination. J Anim Ecol 58:207–224CrossRefGoogle Scholar
  18. Davies NB, Welbergen JA (2008) Cuckoo-hawk mimicry? An experimental test. Proc R Soc B 275:1817–1822PubMedCrossRefGoogle Scholar
  19. Davies NB, Welbergen JA (2009) Social transmission of a host defense against cuckoo parasitism. Science 324:1318–1320PubMedCrossRefGoogle Scholar
  20. Davies NB, Brooke MDL, Kacelnik A (1996) Recognition errors and probability of parasitism determine whether reed warblers should accept or reject mimetic cuckoo eggs. Proc R Soc B 263:925–931CrossRefGoogle Scholar
  21. Davies NB, Butchart SHM, Burke T, Chaline N, Stewart IR (2003) Reed warblers guard against cuckoos and cuckoldry. Anim Behav 65:285–295CrossRefGoogle Scholar
  22. DeWitt TJ, Sih A, Wilson DS (1998) Cost and limits of phenotypic plasticity. Trends Ecol Evol 13:77–81PubMedCrossRefGoogle Scholar
  23. Dingemanse NJ, Wolf M (2013) Between-individual differences in behavioural plasticity within populations: causes and consequences. Anim Behav 85:1031–1039CrossRefGoogle Scholar
  24. Dingemanse NJ, Kazem AJN, Réale D, Wright J (2010) Behavioural reaction norms: animal personality meets individual plasticity. Trends Ecol Evol 25:81–89PubMedCrossRefGoogle Scholar
  25. Feeney WE, Langmore NE (2015) Superb fairy-wrens (Malurus cyaneus) increase vigilance near their nest with the perceived risk of brood parasitism. Auk 132:359–364CrossRefGoogle Scholar
  26. Fordyce JA (2006) The evolutionary consequences of ecological interactions mediated through phenotypic plasticity. J Exp Biol 209:2377–2383PubMedCrossRefGoogle Scholar
  27. Ghalambor CK, McKay JK, Carroll SP, Reznick DN (2007) Adaptive versus non-adaptive phenotypic plasticity and the potential for contemporary adaptation in new environments. Funct Ecol 21:394–407CrossRefGoogle Scholar
  28. Guigueno MF, Sealy SG (2012) Increased investigation of manipulated clutches suggests egg recognition without rejection in a brown-headed cowbird (Molothrus ater) host, the yellow warbler (Setophaga petechia). Auk 129:17–25CrossRefGoogle Scholar
  29. Hale K, Briskie JV (2007) Response of introduced european birds in New Zealand to experimental brood parasitism. J Avian Biol 38:198–204CrossRefGoogle Scholar
  30. Hendry AP (2016) Key questions on the role of phenotypic plasticity in eco-evolutionary dynamics. J Hered 107:25–41PubMedCrossRefGoogle Scholar
  31. Holen ØH, Johnstone RA (2006) Context-dependent discrimination and the evolution of mimicry. Am Nat 167:377–389PubMedGoogle Scholar
  32. Honza M, Požgayová M, Procházka P, Tkadlec E (2007) Consistency in egg rejection behaviour: responses to repeated brood parasitism in the blackcap (Sylvia atricapilla). Ethology 113:344–351CrossRefGoogle Scholar
  33. Kuehn MJ, Peer BD, Rothstein SI (2014) Variation in host response to brood parasitism reflects evolutionary differences and not phenotypic plasticity. Anim Behav 88:21–28CrossRefGoogle Scholar
  34. Kuehn MJ, Peer BD, McCleery RA, Rothstein SI (2016) Yellow warbler defenses are retained in the absence of brood parasitism but enhanced by experience with cowbirds. Behav Ecol 27:279–286CrossRefGoogle Scholar
  35. Lahti DC (2006) Persistence of egg recognition in the absence of cuckoo brood parasitism: pattern and mechanism. Evolution 60:157–168PubMedCrossRefGoogle Scholar
  36. Lang AK, Bollinger EK, Peer BD (2014) Effect of parasite-to-host egg ratio on egg rejection by a Brown-headed cowbird host. Auk 131:694–701CrossRefGoogle Scholar
  37. Langmore NE, Cockburn A, Russell AF, Kilner RM (2009a) Flexible cuckoo chick-rejection rules in the superb fairy-wren. Behav Ecol 20:978–984CrossRefGoogle Scholar
  38. Langmore NE, Stevens M, Maurer G, Kilner RM (2009b) Are dark cuckoo eggs cryptic in host nests? Anim Behav 78:461–468CrossRefGoogle Scholar
  39. Langmore NE, Feeney WE, Crowe-Riddell J, Luan H, Louwrens KM, Cockburn A (2012) Learned recognition of brood parasitic cuckoos in the superb fairy-wren Malurus cyaneus. Behav Ecol 23:799–805CrossRefGoogle Scholar
  40. Lindholm AK (1999) Brood parasitism by the cuckoo on patchy reed warbler populations in Britain. J Anim Ecol 68:293–309CrossRefGoogle Scholar
  41. Lindholm AK (2000) Tests of phenotypic plasticity in reed warbler defences against cuckoo parasitism. Behaviour 137:43–60CrossRefGoogle Scholar
  42. Lindholm AK, Thomas RJ (2000) Differences between populations of reed warblers in defences against brood parasitism. Behaviour 137:25–42CrossRefGoogle Scholar
  43. Lotem A, Nakamura H (1998) Evolutionary equilibria in avian brood parasitism. In: Rothstein S, Robinson S (eds) Parasitic birds and their hosts: studies in coevolution. Oxford University Press, New York, pp 223–235Google Scholar
  44. Lotem A, Nakamura H, Zahavi A (1992) Rejection of cuckoo eggs in relation to host age: a possible evolutionary equilibrium. Behav Ecol 3:128–132CrossRefGoogle Scholar
  45. Lotem A, Nakamura H, Zahavi A (1995) Constraints on egg discrimination and cuckoo-host co-evolution. Anim Behav 49:1185–1209CrossRefGoogle Scholar
  46. Martínez JG, Soler JJ, Soler M, Møller AP, Burke T (1999) Comparative population structure and gene flow of a brood parasite, the great spotted cuckoo (Clamator glandarius), and its primary host, the magpie (Pica pica). Evolution 53:269–278PubMedGoogle Scholar
  47. Martín-Gálvez D, Soler JJ, Martínez JG, Krupa AP, Richard M, Soler M, Møller AP, Burke T (2006) A quantitative trait locus for recognition of foreign eggs in the host of a brood parasite. J Evol Biol 19:543–550PubMedCrossRefGoogle Scholar
  48. Martín-Gálvez D, Soler JJ, Martínez JG, Krupa AP, Soler M, Burke T (2007) Cuckoo parasitism and productivity in different magpie subpopulations predict frequencies of the 457bp allele: a mosaic of coevolution at a small geographic scale. Evolution 61:2340–2348PubMedCrossRefGoogle Scholar
  49. Mendelson TC, Fitzpatrick CL, Hauber ME, Pence CH, RodrÚguez RL, Safran RJ, Stern CA, Stevens JR (2016) Cognitive phenotypes and the evolution of animal decisions. Trends Ecol Evol 31:850–859Google Scholar
  50. Mery F, Burns JG (2010) Behavioural plasticity: an interaction between evolution and experience. Evol Ecol 24:571–583CrossRefGoogle Scholar
  51. Moksnes A, Røskaft E (1989) Adaptations of meadow pipits to parasitism by the common cuckoo. Behav Ecol Sociobiol 24:25–30CrossRefGoogle Scholar
  52. Moksnes A, Røskaft E, Korsnes L (1993) Rejection of cuckoo (Cuculus canorus) eggs by meadow pipits (Anthus pratensis). Behav Ecol 4:120–127CrossRefGoogle Scholar
  53. 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 (Lond 1859) 142:247–258CrossRefGoogle Scholar
  54. Møller AP, Soler JJ (2012) A coevolutionary framework based on temporal and spatial ecology of host-parasite interactions: a missing link in studies of brood parasitism. Chin Birds 3:259–273CrossRefGoogle Scholar
  55. Moran NA (1992) The evolutionary maintenance of alternative phenotypes. Am Nat 139:971–989CrossRefGoogle Scholar
  56. Moskát C, Hauber ME (2007) Conflict between egg recognition and egg rejection decisions in common cuckoo (Cuculus canorus) hosts. Anim Cogn 10:377–386CrossRefPubMedGoogle Scholar
  57. Murren CJ, Auld JR, Callahan H, Ghalambor CK, Handelsman CA, Heskel MA, Kingsolver JG, Maclean HJ, Masel J, Maughan H, Pfennig DW, Relyea RA, Seiter S, Snell-Rood E, Steiner UK, Schlichting CD (2015) Constraints on the evolution of phenotypic plasticity: limits and costs of phenotype and plasticity. Heredity 115:293–301PubMedPubMedCentralCrossRefGoogle Scholar
  58. Nakamura H, Kubota S, Suzuki R (1998) Coevolution between the common cuckoo and its major hosts in Japan. In: Rothstein SI, Robinson SK (eds) Parasitic birds and their hosts: studies in coevolution. Oxford University Press, New York, pp 94–112Google Scholar
  59. Nuismer SL, Thompson JN (2006) Coevolutionary alternation in antagonistic interactions. Evolution 60:2207–2217PubMedCrossRefGoogle Scholar
  60. Nussey DH, Wilson AJ, Brommer JE (2007) The evolutionary ecology of individual phenotypic plasticity in wild populations. J Evol Biol 20:831–844PubMedCrossRefGoogle Scholar
  61. Øien IJ, Honza M, Moksnes A, Roskaft E (1996) The risk of parasitism in relation to the distance from reed warbler nests to cuckoo perches. J Anim Ecol 65:147–153CrossRefGoogle Scholar
  62. Peer BD, Rothstein SI (2010) Phenotypic plasticity in common grackles (Quiscalus quiscula) in response to repeated brood parasitism. Auk 127:293–299CrossRefGoogle Scholar
  63. Peer BD, Rothstein SI, Delaney KS, Fleischer RC (2007) Defence behaviour against brood parasitism is deeply rooted in mainland and island scrub-jays. Anim Behav 73:55–63CrossRefGoogle Scholar
  64. Peer BD, Kuehn MJ, Rothstein SI, Fleischer RC (2011) Persistence of host defence behaviour in the absence of avian brood parasitism. Biol Lett 7:670–673PubMedPubMedCentralCrossRefGoogle Scholar
  65. Piersma T, van Gils JA (2011) The flexible phenotype: a body-centred integration of ecology, physiology, and behaviour. Oxford University Press, OxfordGoogle Scholar
  66. Pigliucci M (2001) Phenotypic plasticity: beyond nature and nurture. Johns Hopkins University Press, BaltimoreGoogle Scholar
  67. Pigliucci M (2005) Evolution of phenotypic plasticity: where are we going now? Trends Ecol Evol 20:481–486PubMedCrossRefGoogle Scholar
  68. Pigliucci M, Murren CJ, Schlichting CD (2006) Phenotypic plasticity and evolution by genetic assimilation. J Exp Biol 209:2362–2367PubMedCrossRefGoogle Scholar
  69. Price TD, Qvarnström A, Irwin DE (2003) The role of phenotypic plasticity in driving genetic evolution. Proc R Soc B 270:1433–1440PubMedCrossRefGoogle Scholar
  70. Robert M, Sorci G (1999) Rapid increase of host defence against brood parasites in a recently parasitized area: the case of village weavers in Hispaniola. Proc R Soc B 266:941–946CrossRefGoogle Scholar
  71. Robert M, Sorci G, Møller A, Hochberg M, Pomiankowski A, Pagel M (1999) Retaliatory cuckoos and the evolution of host resistance to brood parasites. Anim Behav 58:817–824PubMedCrossRefGoogle Scholar
  72. Rodríguez-Gironés MA, Lotem A (1999) How to detect a cuckoo egg: a signal-detection theory model for recognition and learning. Am Nat 153:633–648PubMedGoogle Scholar
  73. Røskaft E, Moksnes A, Stokke BG, Moskát C, Honza M (2002) The spatial habitat structure of host populations explains the pattern of rejection behavior in hosts and parasitic adaptations in cuckoos. Behav Ecol 13:163–168CrossRefGoogle Scholar
  74. Røskaft E, Takasu F, Moksnes A, Stokke BG (2006) Importance of spatial habitat structure on establishment of host defenses against brood parasitism. Behav Ecol 17:700–708CrossRefGoogle Scholar
  75. Rothstein SI (1990) A model system for coevolution: avian brood parasitism. Annu Rev Ecol Syst 21:481–508CrossRefGoogle Scholar
  76. Rothstein SI (2001) Relic behaviours, coevolution and the retention versus loss of host defences after episodes of avian brood parasitism. Anim Behav 61:95–107PubMedCrossRefGoogle Scholar
  77. Ruiz-Raya F, Soler M (2018) Rejection of parasitic eggs: an updated terminology for a complex process. J Avian Biol.  https://doi.org/10.1111/jav.01484
  78. Ruiz-Raya F, Soler M, Sánchez-Pérez LL, Ibáñez-Álamo JD (2015) Could a factor that does not affect egg recognition influence the decision of rejection? PLoS One 10:1–10.  https://doi.org/10.1371/journal.pone.0135624 CrossRefGoogle Scholar
  79. Ruiz-Raya F, Soler M, Roncalli G, Abaurrea T, Ibáñez-Álamo JD (2016) Egg rejection in blackbirds Turdus merula: a by-product of conspecific parasitism or successful resistance against interspecific brood parasites? Front Zool 13:16.  https://doi.org/10.1186/s12983-016-0148-y CrossRefPubMedPubMedCentralGoogle Scholar
  80. Scheiner SM (1993) Genetics and evolution of phenotypic plasticity. Annu Rev Ecol Syst 24:35–68CrossRefGoogle Scholar
  81. Schlichting C, Pigliucci M (1998) Phenotypic evolution: a reaction norm perspective. Sinauer Associates, Sunderland, MAGoogle Scholar
  82. Servedio MR, Lande R (2003) Coevolution of an avian host and its parasitic cuckoo. Evolution 57:1164–1175PubMedCrossRefGoogle Scholar
  83. Snell-Rood E (2013) An overview of the evolutionary causes and consequences of behavioural plasticity. Anim Behav 85:1004–1011CrossRefGoogle Scholar
  84. Soler M (2011) Could egg rejection behaviour be transmitted by social learning? Anim Behav 81:e1–e6CrossRefGoogle Scholar
  85. Soler M (2014) Long-term coevolution between avian brood parasites and their hosts. Biol Rev 89:688–704CrossRefPubMedGoogle Scholar
  86. Soler M, Møller AP (1990) Duration of sympatry and coevolution between the great spotted cuckoo and its magpie host. Nature 343:748–750CrossRefGoogle Scholar
  87. Soler JJ, Soler M (2017) Evolutionary change: facultative virulence by brood parasites and tolerance and plastic resistance by hosts. Anim Behav 125:101–107CrossRefGoogle Scholar
  88. Soler M, Soler JJ, Martínez JG, Møller AP (1994) Micro-evolutionary change in host response to a brood parasite. Behav Ecol Sociobiol 35:295–301CrossRefGoogle Scholar
  89. Soler M, Soler JJ, Martínez JG, Møller AP (1995) Magpie host manipulation by great spotted cuckoos: evidence for an avian mafia. Evolution 49:770–775PubMedCrossRefGoogle Scholar
  90. Soler M, Soler JJ, Martínez JG, Pérez-Contreras T, Møller AP (1998) Micro-evolutionary change and population dynamics of a brood parasite and its primary host: the intermittent arms race hypothesis. Oecologia 117:381–390PubMedCrossRefGoogle Scholar
  91. Soler JJ, Martínez JG, Soler M, Møller AP (1999a) Genetic and geographic variation in rejection behavior of cuckoo eggs by European magpie populations: an experimental test of rejecter-gene flow. Evolution 53:947–956CrossRefPubMedGoogle Scholar
  92. Soler JJ, Sorci G, Soler M, Møller AP (1999b) Change in host rejection behavior mediated by the predatory behavior of its brood parasite. Behav Ecol 10:275–280CrossRefGoogle Scholar
  93. Soler M, Palomino JJ, Martín-Vivaldi M, Soler JJ (2000) Lack of consistency in the response of rufous-tailed scrub robins Cercotrichas galactotes towards parasitic common cuckoo eggs. Ibis 142:151–154CrossRefGoogle Scholar
  94. Soler M, Martín-Vivaldi M, Fernández-Morante J (2012a) Conditional response by hosts to parasitic eggs: the extreme case of the rufous-tailed scrub robin. Anim Behav 84:421–426CrossRefGoogle Scholar
  95. Soler M, Fernández-Morante J, Espinosa F, Martín-Vivaldi M (2012b) Pecking but accepting the parasitic eggs may not reflect ejection failure: the role of motivation. Ethology 118:662–672CrossRefGoogle Scholar
  96. Soler M, Ruiz-Raya F, Roncalli G, Ibáñez-Álamo JD (2017) Relationships between egg-recognition and egg-ejection in a grasp-ejector species. PLoS One 12:e0166283PubMedPubMedCentralCrossRefGoogle Scholar
  97. Stokke BG, Moksnes A, Røskaft E (2005) The enigma of imperfect adaptations in hosts of avian brood parasites. Ornithol Sci 4:17–29CrossRefGoogle Scholar
  98. Stokke BG, Takasu F, Moksnes A, Røskaft E (2007) The importance of clutch characteristics and learning for antiparasite adaptations in hosts of avian brood parasites. Evolution 61:2212–2228PubMedPubMedCentralCrossRefGoogle Scholar
  99. Stokke BG, Hafstad I, Rudolfsen G, Moksnes A, Møller AP, Røskaft E, Soler M (2008) Predictors of resistance to brood parasitism within and among reed warbler populations. Behav Ecol 19:612–620CrossRefGoogle Scholar
  100. Stokke BG, Røskaft E, Moksnes A, Møller AP, Antonov A, FossøY F, Liang W, López-Iborra G, Moskát C, Shykoff JA, Soler M, Vikan JR, Yang C, Takasu F (2016) Disappearance of eggs from nonparasitized nests of brood parasite hosts: the evolutionary equilibrium hypothesis revisited. Biol J Linn Soc 118:215–225CrossRefGoogle Scholar
  101. Takasu F (1998) Modelling the arms race in avian brood parasitism. Evol Ecol 12:969–987CrossRefGoogle Scholar
  102. Thompson JN (2005) The geographic mosaic of coevolution. University of Chicago Press, ChicagoGoogle Scholar
  103. Thorogood R, Davies NB (2013) Reed warbler hosts fine-tune their defenses to track three decades of cuckoo decline. Evolution 67:3545–3555PubMedPubMedCentralCrossRefGoogle Scholar
  104. Welbergen JA, Davies NB (2009) Strategic variation in mobbing as a front line of defense against brood parasitism. Curr Biol 19:235–240PubMedPubMedCentralCrossRefGoogle Scholar
  105. Welbergen JA, Davies NB (2011) A parasite in wolf’s clothing: hawk mimicry reduces mobbing of cuckoos by hosts. Behav Ecol 22:574–579CrossRefGoogle Scholar
  106. Welbergen JA, Davies NB (2012) Direct and indirect assessment of parasitism risk by a cuckoo host. Behav Ecol 23:783–789CrossRefGoogle Scholar
  107. West-Eberhard MJ (2003) Developmental plasticity and evolution. Oxford University Press, OxfordGoogle Scholar
  108. Zölei A, Bán M, Moskát C (2015) No change in common cuckoo Cuculus canorus parasitism and great reed warblers’ Acrocephalus arundinaceus egg rejection after seven decades. J Avian Biol 46:570–576CrossRefGoogle Scholar

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Authors and Affiliations

  1. 1.Departamento de Zoología, Facultad de CienciasUniversidad de GranadaGranadaSpain
  2. 2.Grupo Coevolución, Unidad Asociada al CSICUniversidad de GranadaGranadaSpain

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