JOURNAL OF AVIAN BIOLOGY 33: 366–370, 2002
Rejection of common cuckoo Cuculus canorus eggs in relation to
female age in the bluethroat Luscinia secica
Trond Amundsen, Paul T. Brobakken, Arne Moksnes and Eivin Røskaft
Amundsen, T., Brobakken, P. T., Moksnes, A. and Røskaft, E. 2002. Rejection of
common cuckoo Cuculus canorus eggs in relation to female age in the bluethroat
Luscinia secica. – J. Avian Biol. 33: 366–370.
The evolutionary equilibrium hypothesis explains the existence of both acceptors and
rejecters of brood parasite eggs within a host population as resulting from a balance
between the costs of acceptance and the costs of recognition errors. In such equilibria
conditional responses may play an important role. One such response that has been
demonstrated in one common cuckoo Cuculus canorus host species is that first year,
naive breeders accept parasitic eggs at a higher frequency than older and more
experienced birds do. In the present study we tested whether this is the response in
the bluethroat Luscinia secica. We did not find any difference in rejection behaviour
between first-year breeders and older birds. This finding is discussed in relation to
recognition costs, cuckoo egg mimicry and the bluethroat’s present status as a host.
We conclude that the results are best explained by the evolutionary lag hypothesis.
T. Amundsen, P. T. Brobakken, A. Moksnes (correspondence) and E. Røskaft, Depart -
ment of Zoology, Norwegian Uniersity of Science and Technology, NTNU, Realfag -
bygget, N-7491 Trondheim, Norway. E-mail: Arne.Moksnes@chembio.ntnu.no
Interactions between avian brood parasites and their
hosts have received much attention as model systems
for coevolution in the last three decades (Rothstein
1990, Rothstein and Robinson 1998, Davies 1999,
2000). Interspecific brood parasites lay their eggs in the
nests of other bird species and leave incubation and
subsequent parental care to the foster parents. In the
common cuckoo Cuculus canorus, which parasitises
small passerines, different strains or gentes have
evolved. These gentes have become specialised on dif-
ferent host species whose eggs they typically mimic
(Chance 1940, Baker 1942, Moksnes and Røskaft
1995). After hatching, the cuckoo chick evicts all the
eggs or young of the host and is raised by the foster
parents. The consequence of such parasitism is a selec-
tion pressure on hosts for recognition and rejection of
cuckoo eggs. Rejection of parasitic eggs that match
those of the host poorly will in turn select for better egg
mimicry in the cuckoo. These interactions are hypothe-
sised to result in an arms race between host and para-
site, and may ultimately lead to the evolution of
specialised gentes, as described by Davies and Brooke
(1989a). The arms race hypothesis has been experimen-
tally supported by Davies and Brooke (1989b) and
Moksnes et al. (1990).
Even if it is beneficial for hosts to reject cuckoo eggs,
in many host species a proportion of the individuals
accepts parasitic eggs. In fact, there is a mixture of
rejecters and acceptors within many species (see e.g.
Rothstein 1990). The causes of such variation in rejec-
tion behaviour have been much debated. Two main
hypotheses explain why some species have intermediate
rejection rates: (1) the evolutionary lag hypothesis
(Rothstein 1975a, Dawkins and Krebs 1979, Davies
and Brooke 1989a, Moksnes et al. 1990), and (2) the
evolutionary equilibrium hypothesis (Zahavi 1979, Ro-
hwer and Spaw 1988, Brooker and Brooker 1990, Petit
1991, Lotem et al. 1992, Lotem and Nakamura 1998).
The evolutionary lag hypothesis states that it is al-
ways adaptive to reject parasitic eggs, but such be-
haviour may still not have appeared (no rejection) or
spread to fixation in a host population (Rothstein
1975b). According to the evolutionary equilibrium hy-
pothesis, the response towards the parasitic egg is deter-
mined by a compromise between the costs of
acceptance and the costs of recognition errors.
© JOURNAL OF AVIAN BIOLOGY
JOURNAL OF AVIAN BIOLOGY 33:4 (2002) 366