Abstract
The relationship between brood parasites and their hosts is usually assumed to result in coevolution, and documentation of changes in extant populations should thus be possible. Here we describe how the ejection rate of eggs of an obligate brood parasite, the great spotted cuckoo Clamator glandarius, by its host, the magpie Pica pica, has recently increased in an area in southern Spain. The ejection rate of great spotted cuckoo eggs in naturally parasitized nests of the magpie increased at a rate of 0.5% year' during the period 1982–1992. This result was verified in a number of field experiments using nonmimetic and mimetic model eggs. The rate of increase in ejection rate was 4.7% year-1 for mimetic eggs and 2.3% year-1 for nonmimetic eggs. There were clear differences in parasitism by the great spotted cuckoo between study plots and years, which makes comparisons of rates of parasitism between areas difficult without considering temporal variation. The recent increase in the ejection response of magpies to great spotted cuckoo eggs was not due to magpies using the abundance of cuckoos as a cue to the intensity of parasitism.
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References
Bishop YMM, Fienberg SE, Holland PW (1975) Discrete multivariate analysis: theory and applications. MIT Press, Cambridge
Briskie JV, Scaly SG, Hobson KA (1992) Behavioral defenses against avian brood parasitism in sympatric and allopatric host populations. Evolution 46:334–340
Brooke M de L, Davies NB (1988) Egg mimicry by cuckoos Cuculus canorus in relation to discrimination by hosts. Nature 335:630–632
Brown RJ, Brown MN, Brooke M de L, Davies NB (1990) Reactions of parasitized and unparasitized populations of Acrocephalus warblers to model cuckoo eggs. Nature 132:109–111
Cramp S (ed) (1985) The birds of the Western Palearctic. vol 4. Oxford University Press, Oxford
Cruz A, Wiley JW (1989) The decline of an adaptation in the absence of a presumed selection pressure. Evolution 43:55–62
Davies NB, Brooke M de L (1988) Cuckoo versus reed warblers: Adaptations and counteradaptations. Anim Behav 36:262–284
Davies NB, Brooke M de L (1989) An experimental study of co-evolution between the cuckoo, Cuculus canorus, and its hosts. II. Host egg markings, chick discrimination and general discussion. J Anim Ecol 58:225–236
Dawkins R, Krebs JR (1979) Arms races within and between species. Proc R Soc Lond B 205:489–511
Futuyma DJ, Slatkin M (eds) (1983) Coevolution. Sinauer, Sunderland
Harvey PH, Partridge L (1988) Of cuckoo clocks and cowbirds. Nature 335:586–587
Järvinen O, Väisänen RA (1975) Estimating relative densities of breeding birds by the line transect method. Oikos 26:316–322
Kelly C (1987) A model to explore the rate of spread of mimicry and rejection in hypothetical populations of cuckoos and their hosts. J Theor Biol 125:283–299
Lotem A, Nakamura H, Zahavi A (1992) Rejection of cuckoo eggs in relation to host age: a possible evolutionary equilibium. Behav Ecol 3:128–132
Moksnes A, Roskaft E (1989) Adaptations of meadow pipits to parasitism by the common cuckoo. Behav Ecol Sociobiol 24:25–30
Nakamura H (1990) Brood parasitism by the cuckoo Cuculus canorus in Japan and the start of new parasitism on the azurewinged magpie Cyanopica cyanea. Jpn J Ornithol 39:1–8
Payne RB (1973) Individual laying histories and the clutch size and numbers of eggs of parasitic cuckoos. Condor 75:414–438
Payne RB (1977) The ecology of brood parasitism in birds. Annu Rev Ecol Syst 8:1–28
Rothstein SI (1974) Mechanisms of avian egg recognition: possible learned and innate factors. Auk 91:796–807
Rothstein SI (1977) Cowbird parasitism and egg recognition of the northern oriole. Wilson Bull 89:21–32
Rothstein SI (1978) Mechanisms of avian egg recognition: Additional evidence for learned responses. Anim Behav 26:671–677
Rothstein SI (1990) A model system for coevolution: avian brood parasitism. Annu Rev Ecol Syst 21:481–508
Siegel S, Castellan NJ Jr (1988) Nonparametric statistics for the behavioral sciences. McGraw-Hill, New York
Sokal RR, Rohlf FJ (1981) Biometry, 2nd edn. Freeman, San Francisco
Soler M (1990) Relationship between the great spotted cuckoo, Clamator glandarius, and its corvid hosts in a recently colonized area. Ornis Scand 21:212–223
Soler M, Moller AP (1990) Duration of sympatry and coevolution between the great spotted cuckoo and its magpie host. Nature 343:748–750
Soler M, Soler JJ (1991) Growth and development of great spotted cuckoos and their magpie hosts. Condor 93:49–54
Takasu F, Kawasaki K, Nakamura H, Cohen JE, Shigesada N (1993) Modeling the population dynamics of a cuckoo-host association and the evolution of host defences. Am Nat 142:819–839
Zuñiga JM, Redondo T (1992) No evidence for variable duration of sympatry between the great spotted cuckoo and its magpie host. Nature 359:410–411
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Soler, M., Martinez, J.G., Soler, J.J. et al. Micro-evolutionary change in host response to a brood parasite. Behav Ecol Sociobiol 35, 295–301 (1994). https://doi.org/10.1007/BF00170710
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DOI: https://doi.org/10.1007/BF00170710