Brood parasitic birds constitute a model system for the study of coevolution.Such parasites are unique by having evolved unusually thick eggshells for their body size.ick eggshells have been hypothesized to evolve as 1) a means of preventing damage to parasite eggs when the brood parasite lays its egg at a distance from the host clutch(the laying damage hypothesis);2) a consequence of host puncture ejection(the puncture resistance hypothesis);3) a means for the brood parasite to allocate calcium to development of a disproportionately large skeleto-muscular system in evicting parasite chicks(the chick vigour hypothesis);or 4) a means of protecting the cuckoo embryo from microorganisms in the nest of the host(the anti-bacterial protection hypothesis).Here we review the literature studying the evolutionary mechanisms promoting thick eggshells in avian brood parasites,and provide proposals for future studies to test their validity.Available data are insu cient to rigorously test exclusive predictions and assumptions of these not necessarily exclusive hypotheses,although the laying damage and the puncture resistance hypotheses seem to currently be the most well supported alternatives.We discuss how quanti cation of rejection modes(grasp ejection,puncture ejection and desertion) may disclose the validity of the puncture resistance hypothesis,and nally we provide perspectives for future research on testing this speci c hypothesis.
Anton ANTONOVBrd G.STOKKEFrode FOSSY梁伟Arne MOKSNESEivin RSKAFT杨灿朝Anders P.MLLER
Polymorphism in egg coloration is prominent in the Common Cuckoo (Cuculus canorus) and a common host, the Ashy-throated Parrotbill (Paradoxornis alphonsianus). Egg polymorphism has probably evolved as a consequence of frequency-dependent selection in both host and parasite, and has, according to human vision, resulted in discrete immaculate white, pale blue and blue egg phenotypes within a single population. However, egg mimicry assessment is not always straightforward, and previous studies have shown that human based comparisons applied to the coloration of bird eggs may be inadequate. Here, we objectively quantify egg color of both parasite and host by spectrophotometry and assess egg mimicry of the Common Cuckoo to the eggs of its Ashy-throated Parrotbill host. Our results revealed that egg reflectance spectra agree well with the assessment based on human vision that cuckoo eggs mimic those of the parrotbill host, in both visible (VIS) and ultraviolet (UV) ranges. However, the white cuckoo egg shows slightly poorer mimicry than the blue cuckoo egg in corresponding host clutches. We suggest that the white parrotbill egg morph (and subsequently the whitish cuckoo egg color) may have evolved after the evolution of the blue egg morph due to strong selection from parasites in the cuckoo-parrotbill system.
Rates of brood parasitism vary extensively among host species and populations of a single host species. In this study, we documented and compared parasitism rates of two sympatric hosts, the Oriental Reed Warbler （Acrocephalus orientalis） and the Reed Parrotbill （Paradoxornis heudei）, in three populations in China. We found that the Common Cuckoo （Cuculus canorus） is the only parasite using both the Oriental Reed Warbler and Reed Parrotbill as hosts, with a parasitism rate of 22.4%-34.3% and 0%-4.6%, respectively. The multiple parasitism rates were positively correlated with local parasitism rates across three geographic populations of Oriental Reed Warbler, which implies that higher pressure of parasitism lead to higher multiple parasitism rate. Furthermore, only one phenotype of cuckoo eggs was found in the nests of these two host species. Our results lead to two conclusions： （1） The Oriental Reed Warbler should be considered the major host of Common Cuckoo in our study sites; and （2） obligate parasitism on Oriental Reed Warbler by Common Cuckoo is specialized but flexible to some extent, i.e., using Reed Parrotbill as a secondary host. Further studies focusing on egg recognition and rejection behaviour of these two host species should be conducted to test our predictions.
Interaction between a parasite and its host could lead to a co-evolutionary arms race. Cuckoo-host system is among the most studied of all brood parasite systems, but the cuckoos of Asia, on the other hand, are much less well known. China has the most abundant cuckoo species in Asia. Many of these co-occur in sympatric areas, posing a potential risk of mis-identification of cuckoo nestlings, especially in Cuculus species. In this study we have provided a practical criterion to identify cuckoo nestlings species in the field and performed molecular phylogeny to confirm our empirical results. These results indicate that two distinct characteristics of cuckoo nestlings, i.e., the gape color pattern and feather traits can be considered as reliable species identification. To our knowledge, this is the first report for species identification of Cuculus nestlings through molecular analysis.
In this exposé we provide the first review of host use by brood parasitic cuckoos in a multiple-cuckoo system in China, based on our own long-term field data and a compilation of observations obtained from the literature. In total, we found that 11 species of cuckoos utilized altogether 55 host species. These hosts belong to 15 families, in which Sylviidae, Turdidae and Timaliidae account for 22.6%, 20.8% and 17.0% of parasitism records, respectively. The Common Cuckoo (Cuculus canorus) had the widest range of host species, accounting for 45.5% of the total number of parasitized species (25 in 10 families) of all parasitism records and is the most frequent brood parasite in the country. Cuckoo species differed in their egg coloration and the extent of egg polymorphism with most of them, e.g. the Common Cuckoo, the Lesser Cuckoo (C. poliocephalus) and the Plaintive Cuckoo (Cacomantis merulinus) laying well mimetic eggs with respect to their hosts based on human being’s visual observations, while others such as the Large Hawk-cuckoo (C. sparverioides), the Himalayan Cuckoo (C. saturatus) and the Asian Emerald Cuckoo (Chrysococcyx maculatus) usually laid non-mimetic eggs. The use of cuckoo hosts and egg color variation in China are compared with those in other parts of their ranges in Asia.
