Evicting cuckoo nestlings from the nest: a new anti-parasitism behaviour (original) (raw)
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Behavioral Ecology and Sociobiology, 2010
Hosts of the common cuckoo (Cuculus canorus), an avian brood parasite, develop antiparasite defense mechanisms to increase their reproductive success. Ejection of the parasite egg and desertion of the parasitized nest are the most typical adaptations in response to brood parasitism, but nest desertion may also occur in response to partial clutch reduction, independently from parasitism. Some great reed warblers (Acrocephalus arundinaceus) showed both mechanisms in the same incidence of cuckoo parasitism: in 18% of successful ejections of the parasite eggs, they deserted their nests. We studied if such cases of post-ejection nest-desertion are caused by brood parasitism or reduced clutch value. We experimentally parasitized clutches consisting of five or three host eggs with two painted conspecific eggs to mimic parasitic eggs, as multiple parasitism is frequent in the area. Although hosts ejected these parasitic eggs in both clutch categories (100% and 67% for the larger and smaller inital clutch sizes, respectively), we found that after manipulation, postejection nest-desertion frequently occurred at small (3-egg) clutches (40%), but rarely at large (5-egg) clutches (17%). The same phenomenon also occurred when unparasitized 3-egg clutches were reduced by two eggs, but not when 5-egg clutches were reduced in the same way. A logistic regression model revealed that only initial clutch size affected nest desertion of parasitized nests in our experiments. Therefore, we conclude that post-ejection nest-desertion is not a second antiparasite mechanism, which might serve as a redundant antiparasite defense, but a reaction to typically small and further decreased clutch size. Keywords Cuckoo. Great reed warbler. Antiparasite defense. Clutch size. Clutch reduction The common cuckoo (Cuculus canorus, hereafter "cuckoo") is a well-known brood parasite, which parasitizes more than a hundred small passerine species breeding in the Palearctic (Wyllie 1981; Davies 2000; Payne 2005). However, the number of regularly used hosts is much smaller, probably just over 20, and at least 17 host-specific races of the cuckoo (the so-called "gentes") with developed egg mimicry were previously found in Europe (Moksnes and Røskaft 1995; Alvarez 1994; Antonov et al. 2007), with additional species in Asia (Higuchi 1998; Lee and Yoo 2004; Takasu et al. 2009). The coevolutionary processes between cuckoos and their avian hosts are typically explained as a coevolutionary arms race (Dawkins and Communicated by M. Soler
Cuckoos versus hosts in insects and birds: adaptations, counter-adaptations and outcomes
Biological Reviews
Avian parents and social insect colonies are victimized by interspecific brood parasites-cheats that procure costly care for their dependent offspring by leaving them in another species' nursery. Birds and insects defend themselves from attack by brood parasites; their defences in turn select counter-strategies in the parasite, thus setting in motion antagonistic co-evolution between the two parties. Despite their considerable taxonomic disparity, here we show striking parallels in the way that co-evolution between brood parasites and their hosts proceeds in insects and birds. First, we identify five types of co-evolutionary arms race from the empirical literature, which are common to both systems. These are: (a) directional co-evolution of weaponry and armoury; (b) furtiveness in the parasite countered by strategies in the host to expose the parasite; (c) specialist parasites mimicking hosts who escape by diversifying their genetic signatures; (d) generalist parasites mimicking...
Persistence of host defence behaviour in the absence of avian brood parasitism
Biology Letters, 2011
The fate of host defensive behaviour in the absence of selection from brood parasitism is critical to long-term host–parasite coevolution. We investigated whether New World Bohemian waxwings Bombycilla garrulus that are allopatric from brown-headed cowbird Molothrus ater and common cuckoo Cuculus canorus parasitism have retained egg rejection behaviour. We found that egg rejection was expressed by 100 per cent of Bohemian waxwings. Our phylogeny revealed that Bohemian and Japanese waxwings Bombycilla japonica were sister taxa, and this clade was sister to the cedar waxwing Bombycilla cedrorum . In addition, there was support for a split between Old and New World Bohemian waxwings. Our molecular clock estimates suggest that egg rejection may have been retained for 2.8–3.0 Myr since New World Bohemian waxwings inherited it from their common ancestor with the rejecter cedar waxwings. These results support the ‘single trajectory’ model of host–brood parasite coevolution that once hosts ...
The evolution of egg rejection by cuckoo hosts in Australia and Europe
Behavioral Ecology, 2005
Exploitation of hosts by brood parasitic cuckoos is expected to stimulate a coevolutionary arms race of adaptations and counteradaptations. However, some hosts have not evolved defenses against parasitism. One hypothesis to explain a lack of host defenses is that the life-history strategies of some hosts reduce the cost of parasitism to the extent that accepting parasitic eggs in the nest is evolutionarily stable. Under this hypothesis, it pays hosts to accept cuckoo eggs if (1) the energetic cost of raising the cuckoo is low, (2) there is time to renest, and clutch size is small. We parasitized the nests of host and nonhost species with nonmimetic model eggs to test whether the evolution of egg recognition by cuckoo hosts could be explained by life-history variables of the host. The most significant factor explaining rates of rejection of model eggs was whether or not a species was a cuckoo host, with hosts rejecting model eggs at a higher rate than nonhosts. Egg-rejection rates were also explained by visibility within the nest and by cuckoo mass. We found little support for the life-history model of egg rejection. Our results suggest that parasitism is always sufficiently costly to select for host defenses and that the evolution of defenses may be limited by proximate constraints such as visibility within the nest.
Foreign egg retention by avian hosts in repeated brood parasitism: why do rejecters accept?
Behavioral Ecology and Sociobiology, 2014
Great reed warblers (Acrocephalus arundinaceus) are frequently parasitized by egg-mimetic common cuckoos (Cuculus canorus) in Hungary, and these hosts reject about a third of parasitic eggs. The timing of parasitism is important, in that the probability of rejection decreases with advancing breeding stages in this host. Also, egg rejection is more common when a clutch is parasitized by a single foreign egg, compared to parasitism by multiple eggs. We repeatedly parasitized great reed warbler clutches with moderately mimetic foreign eggs, either with (1) one foreign egg (single parasitism) and, after 3 days, by all foreign eggs (multiple parasitism), or (2) all foreign eggs and, 3 days later, by only one foreign egg. Hosts ejected 26-53 % of the experimental parasitic eggs in the first stage of the repeated parasitism, but almost all eggs were accepted in the second stage, irrespective of whether the clutch was singly or multiply parasitized. Video-taping of the behavioural responses of hosts to experimental parasitism revealed no evidence for sensory constraints on foreign-egg recognition, because hosts recognized and pecked the parasitic eggs as frequently in the second stage of repeated parasitism, as they did in the first stage. We suggest that the relative timing of parasitism (laying vs. incubation stage), rather than learning to accept earlier-laid foreign eggs, results in higher acceptance rates of cuckoo eggs in repeated parasitism, because there is decreasing natural cuckoo parasitism on this host species and, hence, less need for antiparasitic defences, with the advancing stages of breeding.
Evidence for egg discrimination preceding failed rejection attempts in a small cuckoo host
Biology Letters, 2009
Given the high costs of avian obligate brood parasitism, host individuals are selected to reject parasitic eggs they recognize as foreign. We show that rejection may not necessarily follow egg discrimination when selective removal of the parasitic egg is difficult. We studied egg rejection behaviour in a small host of the common cuckoo Cuculus canorus, the eastern olivaceous warbler Hippolais pallida, by experimental parasitism with model and real non-mimetic cuckoo eggs and video recordings of host behaviour. Hosts pecked 87 per cent (20 out of 23) of the model eggs but eventually accepted 43.5 per cent (10 out of 23) of them. A similar pattern was found for real cuckoo eggs, which were all pecked, but as many as 47 per cent (7 out of 15) of them were accepted. To our knowledge, this is the first demonstration of a cuckoo host discriminating against real parasitic eggs but often accepting them. Our results also show that in host species experiencing difficulties in performing puncture ejection, non-mimetic cuckoo eggs may avoid rejection by means of their unusually high structural strength.
Cuckoo hosts shift from accepting to rejecting parasitic eggs across their lifetime
Evolution; international journal of organic evolution, 2014
One of the best-known outcomes of coevolution between species is the rejection of mimetic parasite eggs by avian hosts, which has evolved to reduce costly cuckoo parasitism. How this behavioral adaptation varies along the life of individual hosts remains poorly understood. Here, we identify for the first time, lifetime patterns of egg rejection in a parasitized long-lived bird, the magpie Pica pica and show that, during the years they were studied, some females accept, others reject, and some others modify their response to model eggs, in all cases switching from acceptance to rejection. Females tested in their first breeding attempt always accepted the model egg, even those individuals whose mothers were egg rejecters. A longitudinal analysis showed that the probability of egg rejection increased with the relative age of the female, but was not related to the risk of parasitism in the population. We conclude that ontogeny plays a fundamental role in the process leading to egg rejec...