Brood Parasitic Cuckoos Research Articles

"Isolation by Gentes with Asymmetric Migration" shapes the genetic structure of the common cuckoo in China.

Amid coevolutionary arms races between brood parasitic birds and their diverse host species, the formation of host-specific races, or gentes, has drawn significant research focus. Nevertheless, numerous questions about gentes evolutionary patterns persist. Here, we investigated the potential for gentes evolution across multiple common cuckoo (Cuculus canorus) populations parasitizing diverse host species in China. Using maternal (mitochondrial and W-linked DNA) and biparental (autosomal and Z-linked DNA) markers, we found consistent clustering of cuckoo gentes (rather than geographical populations) into distinct clades in matrilineal gene trees, indicating robust differentiation. In contrast, biparental markers indicated intermixing of all gentes, suggesting asymmetric gene flow regardless of geography. Unlike the mitonuclear discordance commonly resulting from incomplete lineage sorting, adaptive introgression, or demographic disparities, the observed pattern in brood parasitic cuckoos might reflect biased host preferences between sexes. We hereby present the "Isolation by Gentes with Asymmetric Migration" model. According to this model, the maternal line differentiation of the common cuckoo in China is potentially driven by host preferences in females, whereas males maintained the integrity of the cuckoo species through random mating. To achieve this, cuckoo males could perform flexible migration among gentes or engage in early copulation with females before reaching the breeding sites, allowing female cuckoos to store sperm from various gentes. Future studies collecting additional samples from diverse cuckoo gentes with overlapping distribution and investigating the migratory and copulation patterns of each sex would enhance our understanding of sex-biased differentiation among cuckoo populations in China.

Coevolution with hosts underpins speciation in brood-parasitic cuckoos.

Coevolution between interacting species is thought to increase biodiversity, but evidence linking microevolutionary processes to macroevolutionary patterns is scarce. We leveraged two decades of behavioral research coupled with historical DNA analysis to reveal that coevolution with hosts underpins speciation in brood-parasitic bronze-cuckoos. At a macroevolutionary scale, we show that highly virulent brood-parasitic taxa have higher speciation rates and are more likely to speciate in sympatry than less-virulent and nonparasitic relatives. We reveal the microevolutionary process underlying speciation: Hosts reject cuckoo nestlings, which selects for mimetic cuckoo nestling morphology. Where cuckoos exploit multiple hosts, selection for mimicry drives genetic and phenotypic divergence corresponding to host preference, even in sympatry. Our work elucidates perhaps the most common, but poorly characterized, evolutionary process driving biological diversification.

Lack of host specialization despite selective host use in brood parasitic cuckoo catfish.

Host-parasite dynamics involve coevolutionary arms races, which may lead to host specialization and ensuing diversification. Our general understanding of the evolution of host specialization in brood parasites is compromised by a restricted focus on bird and insect lineages. The cuckoo catfish (Synodontis multipunctatus) is an obligate parasite of parental care of mouthbrooding cichlids in Lake Tanganyika. Given the ecological and taxonomic diversity of mouthbrooding cichlids in the lake, we hypothesized the existence of sympatric host-specific lineages in the cuckoo catfish. In a sample of 779 broods from 20 cichlid species, we found four species parasitized by cuckoo catfish (with prevalence of parasitism of 2%-18%). All parasitized cichlids were from the tribe Tropheini, maternal mouthbrooders that spawn over a substrate (rather than in open water). Phylogenetic analysis based on genomic (ddRAD sequencing) and mitochondrial (Dloop) data from cuckoo catfish embryos showed an absence of host-specific lineages. This was corroborated by analyses of genetic structure and co-ancestry matrix. Within host species, parasitism was not associated with any individual characteristic we recorded (parent size, water depth), but was costly as parasitized parents carried smaller clutches of their own offspring. We conclude that the cuckoo catfish is an intermediate generalist and discuss costs, benefits and constraints of host specialization in this species and brood parasites in general.

Multiple parasitism promotes facultative host acceptance of cuckoo eggs and rejection of cuckoo chicks

Many hosts of brood-parasitic cuckoos reject foreign eggs from the nest. Yet where nests commonly receive more than one cuckoo egg, hosts might benefit by instead accepting parasite eggs. This is because cuckoos remove an egg from the nest before adding their own, and keeping cuckoo eggs in the nest reduces the odds that further host eggs are removed by subsequent cuckoos. This ‘clutch dilution effect’ has been proposed as a precondition for the evolution of cuckoo nestling eviction by hosts, but no previous studies have tested this in a host that rejects cuckoo nestlings. We tested the clutch dilution hypothesis in large-billed gerygones, Gerygone magnirostris, which are multiply parasitized by little bronze-cuckoos, Chalcites minutillus. Gerygones evict cuckoo nestlings but accept cuckoo eggs. Consistent with multiple parasitism favouring egg acceptance, we found gerygone egg survival was higher under scenarios of cuckoo egg acceptance than rejection. Yet gerygones were also flexible in their egg acceptance, with 61% abandoning clutches if they contained only cuckoo eggs. Our results thus confirm a clutch dilution effect in gerygones and suggest that multiple parasitism might favour a facultative response to cuckoo eggs, whereby hosts accept or reject cuckoo eggs depending on clutch composition.

Low incidence of cannibalism among brood parasitic cuckoo catfish embryos.

Brood parasites have demanding needs of host resources. Brood parasitic offspring are highly competitive and frequently cause the failure of host broods and the survival of a single parasitic offspring. Accordingly, virulent brood parasites lay a single egg in the same host nest to avoid sibling competition. In the cuckoo catfish (Synodontis multipunctatus), which parasitize mouthbrooding cichlid fishes in Lake Tanganyika, the modes of host and parasite oviposition lead to frequent cases of multiple parasitism. We experimentally tested the prediction that multiple parasitism leads to frequent cannibalism among offspring. Cuckoo catfish embryos prey upon host offspring to obtain nourishment during their 3-week development in the host buccal cavity and may also consume conspecific embryos. The potential benefits of cannibalism in the system are, therefore, twofold; to decrease competition for limited resources (i.e., host brood with rich yolk sacs) and to directly obtain nourishment by consuming rivals. We found that cannibalism indeed provided measurable benefits in terms of increased growth of the cannibals, but cannibalism was rare and typically occurred once all host offspring had been consumed. This implies that cannibalism among cuckoo catfish embryos emerges to mitigate starvation rather than eliminate competition.

A novel method to collect sperm from brood parasitic cuckoos: Urodeum stimulation (UroS) method

Sperm competition has been studied in numerous species as a representative example of postcopulatory sexual selection, where sampling sperm from male is the most basic and important step. Sperm collection can be tricky in birds, however, because unlike mammals, the genitals of birds are generally latent in the cloacal region and their characteristics vary among species. Various methods to collect sperm from different birds have been tested, such as cloacal massage, feces collection, and electro-stimulation, but their applicability varies depending on species. In this study, we introduced the urodeum stimulation method (UroS method) to collect sperm from Cuculus cuckoos, such as the Common Cuckoo (C. canorus). These species are expected to have interesting patterns of pair bonding and sperm competition because of their unique breeding strategy called brood parasitism; however, it remains unexplored. In this study, we described the application of our new method to expel semen from male common cuckoos, measured the volume of semen collected, checked the presence of sperm in the semen sample, and finally estimated its success rate among 82 males. Samples were successfully collected from 76 cuckoos (approximately 93%) and the colors and volumes of the samples were very diverse. Sperm was present in 43 of these samples (57%), showing a sperm observation rate approximately twice as high as that of the conventional cloacal massage method. We believe that this novel method will contribute to a better understanding of postcopulatory sexual selection in avian brood parasites and facilitate the process of sperm collection and artificial insemination in other medium-sized birds.

Avian brood parasites, species assemblage, and bird diversity: A case study using a grid-based survey in South Korea

Identifying proper surrogate species or groups is a challenging but critical step in the application of surrogate species approaches in biodiversity conservation because their effectiveness can vary according to biological communities. Recently, the brood parasitic common cuckoo, Cuculus canorus, has been suggested as a surrogate for describing biodiversity, primarily based on its strong parasitic relationship with other host species. However, the efficiency of cuckoo surrogates has been challenged because of the potential limitations of the methodological approaches. Furthermore, its generality rarely has been explicitly tested in other parasitic species with local biodiversity data collected through conventional schemes such as grid-based sampling. Using bird survey data obtained from a grid-based sampling scheme in South Korea, we evaluated the surrogate efficiency of five cuckoo species for bird diversity (species richness and phylogenetic diversity) and generated surrogate species groups. We found that among the five parasitic cuckoo species breeding in South Korea, the common cuckoo and the Indian cuckoo C. micropterus were effective surrogate species. Among these, only the common cuckoo belonged to the best surrogate species group together with its major host species; the Indian cuckoo showed less effective surrogate efficiency than the common cuckoo. In conclusion, our study shows that the common cuckoo, as a single species and a member of a species assemblage, is an effective indicator species for bird diversity in grid-based survey data. However, the result that not all parasitic cuckoo species performed a surrogate role effectively implies that multiple functions may be associated with the surrogate efficiency of brood parasitic cuckoos, along with the importance of host-parasite relationships.

Thicker eggshells are not predicted by host egg ejection behaviour in four species of Australian cuckoo

Defences of hosts against brood parasitic cuckoos include detection and ejection of cuckoo eggs from the nest. Ejection behaviour often involves puncturing the cuckoo egg, which is predicted to drive the evolution of thicker eggshells in cuckoos that parasitise such hosts. Here we test this prediction in four Australian cuckoo species and their hosts, using Hall-effect magnetic-inference to directly estimate eggshell thickness in parasitised clutches. In Australia, hosts that build cup-shaped nests are generally adept at ejecting cuckoo eggs, whereas hosts that build dome-shaped nests mostly accept foreign eggs. We analysed two datasets: a small sample of hosts with known egg ejection rates and a broader sample of hosts where egg ejection behaviour was inferred based on nest type (dome or cup). Contrary to predictions, cuckoos that exploit dome-nesting hosts (acceptor hosts) had significantly thicker eggshells relative to their hosts than cuckoos that exploit cup-nesting hosts (ejector hosts). No difference in eggshell thicknesses was observed in the smaller sample of hosts with known egg ejection rates, probably due to lack of power. Overall cuckoo eggshell thickness did not deviate from the expected avian relationship between eggshell thickness and egg length estimated from 74 bird species. Our results do not support the hypothesis that thicker eggshells have evolved in response to host ejection behaviour in Australian cuckoos, but are consistent with the hypothesis that thicker eggshells have evolved to reduce the risk of breakage when eggs are dropped into dome nests.

Linking individual attributes and host specialization in brood parasitic cuckoos

Generalist avian brood parasites vary considerably in their degree of host specialization (e.g., number of hosts); some parasitize the nests of just a few host species, whereas others exploit more than 100 species. Several factors, including habitat range, habitat type, and geographic location, have been suggested to account for these variations. However, inter-specific differences in individual attributes, such as personality and plasticity, have rarely been considered as potential factors of such variation, despite their potential relationship to, for example, range expansion. Using cage experiments, we tested the hypothesis that parasitic species exploiting more host species may be more active and exploratory. To this end, we quantified behaviors exhibited by two Cuculus cuckoos (Common Cuckoo C. canorus and Oriental Cuckoo C. optatus) that vary greatly in their number of host species. Specifically, we evaluated exploratory behavior displayed by birds in the cage, such as the number of movements, head-turning, wing-flapping, and stepping. The Common Cuckoo, which has a higher number of host species, tended to exhibit higher levels of exploratory behaviors than the Oriental Cuckoo. Our study showed that the two cuckoo species exhibited different exploratory levels, as predicted by the differences in their number of hosts. Further studies regarding the causality between individual attributes and host specialization with improved experimental methodology would greatly enhance our understanding of the role of individual characteristics in the coevolution of avian brood parasites and their hosts.

First recorded evidence of ejection of a cuckoo egg in a fairy-wren species

Brood-parasitic cuckoos lay their eggs in the nests of other birds, abandoning parental care to their hosts. Many host species have evolved defences to escape or reduce the costs associated with cuckoo parasitism. Superb Fairy-wrens Malurus cyaneus, which are a host to several cuckoo species in Australia, can distinguish cuckoo eggs based on their size or shape, or by using indirect cues such as the timing of egg laying or the presence of an adult cuckoo near the nest. They have previously been shown to reject cuckoo eggs by methods of egg burial or abandonment. These methods are likely to be costlier than ejecting the cuckoo egg from the nest (as seen in some other host species), because of the complete failure of the reproductive attempt, in addition to the costs associated with renesting. In this study, we document with photograph and video footage an incident of a Fan-tailed Cuckoo Cacomantis flabelliformis parasitising a nest of a Superb Fairy-wren in the Australian National Botanic Gardens, Canberra. Shortly after the parasitism event occurred, we recorded the female Fairywren returning to the nest and ejecting the single Cuckoo egg. To our knowledge, this footage represents the first evidence of ejection of a cuckoo egg in this species.

Reed Warbler Hosts Do Not Fine-Tune Mobbing Defenses During the Breeding Season, Even When Cuckoos Are Rare

Hosts of brood parasitic cuckoos often employ mobbing attacks to defend their nests and, when mobbing is costly, hosts are predicted to adjust their mobbing to match parasitism risk. While evidence exists for fine-tuned plasticity, it remains unclear why mobbing does not track larger seasonal changes in parasitism risk. Here we test a possible explanation from parental investment theory: parents should defend their current brood more intensively as the opportunity to replace it declines (re-nesting potential), and therefore “counteract” any apparent seasonal decline to match parasitism risk. We take advantage of mobbing experiments conducted at two sites where reed warblers (Acrocephalus scirpaceus) experience (in Italy), or do not experience (in Finland), brood parasitism. We predicted that mobbing of cuckoos should be higher overall in Italy, but remain constant over the season as in other parasitised sites, whereas in Finland where cuckoos do not pose a local threat, we predicted that mobbing should be low at the beginning of the season but increase as re-nesting potential declined. However, while cuckoos were more likely to be mobbed in Italy, we found little evidence that mobbing changed over the season at either the parasitized or non-parasitized sites. This suggests that re-nesting potential has either little influence on mobbing behavior, or that its effects are obscured by other seasonal differences in ecology or experience of hosts.

Imperfect mimicry of host begging calls by a brood parasitic cuckoo: a cue for nestling rejection by hosts?

Coevolutionary interactions between avian brood parasites and their hosts often lead to the evolution of discrimination and rejection of parasite eggs or chicks by hosts based on visual cues, and the evolution of visual mimicry of host eggs or chicks by brood parasites. Hosts may also base rejection of brood parasite nestlings on vocal cues, which would in turn select for mimicry of host begging calls in brood parasite chicks. In cuckoos that exploit multiple hosts with different begging calls, call structure may be plastic, allowing nestlings to modify their calls to match those of their various hosts, or fixed, in which case we would predict either imperfect mimicry or divergence of the species into host-specific lineages. In our study of the little bronze-cuckoo (LBC) Chalcites minutillus and its primary host, the large-billed gerygone Gerygone magnirostris, we tested whether: (1) hosts use nestling vocalizations as a cue to discriminate cuckoo chicks; (2) cuckoo nestlings mimic the host begging calls throughout the nestling period; and (3) the cuckoo begging calls are plastic, thereby facilitating mimicry of the calls of different hosts. We found that the begging calls of LBCs are most similar to their gerygone hosts shortly after hatching (when rejection by hosts typically occurs) but become less similar as cuckoo chicks get older. Begging call structure may be used as a cue for rejection by hosts, and these results are consistent with gerygone defenses selecting for age-specific vocal mimicry in cuckoo chicks. We found no evidence that LBC begging calls were plastic.

Empirical evidence of different egg morphs that match host eggs in the brush cuckoo (Cacomantis variolosus)

ABSTRACT One of the most efficient defences against obligate brood parasitism in birds is egg ejection, where a host recognises and removes the parasitic egg from the nest. This defence often selects for egg mimicry in parasitic species to reduce the likelihood of egg ejection. If a parasite uses multiple host species with distinctive egg types, this could lead to the evolution of egg gentes (host-specific egg types) in the parasite. There is observational evidence that the brood parasitic Brush Cuckoo (Cacomantis variolosus) might exhibit egg gentes, but there has been no objective study conducted to determine how closely eggs of this cuckoo species resemble those of its hosts from a bird’s visual perspective. Using objective measurements to quantify egg appearance, we found that Brush Cuckoos exhibit at least two egg morphs that closely match the eggs of two of its primary hosts in colour, luminance and volume. While the determination of actual egg gentes in the Brush Cuckoo was beyond the scope of our study, our results are a first and necessary step in determining whether egg gentes might exist in this species. We suggest at least a third egg morph matching another primary host (or at least the genus of that host) might exist, but more data would be necessary to confirm this. Additionally, we provide a mechanism researchers can use to help distinguish between Brush Cuckoo eggs that are closely matched to their host eggs for future studies in this system.

How do brood-parasitic cuckoos reconcile conflicting environmental and host selection pressures on egg size investment?

Brood-parasitic cuckoos lay their eggs in the nests of other birds and thereafter abandon their young to the care of the host. Thus, all maternal investment is restricted to investment in the egg. Optimal investment at this stage is likely to have a large impact on maternal reproductive success. Many bird species optimize the size of their eggs to suit both the prevailing environmental conditions and the number of individuals that will provide care to the chicks. However, relatively few cues are available to avian brood parasites to facilitate optimal investment in their eggs. Moreover, optimization of egg size to suit environmental conditions or the social structure of the host group may be constrained by stronger selection for egg mimicry, which reduces the likelihood of detection and rejection of foreign eggs by the host. We aimed to test how the conflicting selection pressures of (1) selection for large eggs in harsh environmental conditions versus (2) rejection of large eggs by hosts interact to influence the size and shape of Horsfield's bronze-cuckoo, Chalcites basalis , eggs. Using a sliding window approach to investigate periods of climate sensitivity, we show that climatic variables did not predict egg size. Nor did cuckoos modify their egg size or shape in relation to the group size of the host (superb fairy-wren, Malurus cyaneus ). Conversely, host defences did appear to have influenced cuckoo egg morphology: eggs that were relatively short and round had a higher probability of being abandoned by the host than eggs that were long and narrow. This suggests that host defences are the overriding selection pressure on cuckoo egg morphology, and, unlike their hosts, cuckoos do not adapt their eggs to the prevailing climate or host group size. • Female brood-parasitic cuckoos invest only in the egg. • Selection pressures of host rejection and environment on egg size conflict. • Sliding window approach was used to investigate periods of climate sensitivity. • Host defences are the overriding selection pressure on cuckoo egg morphology. • Hosts use adult cuckoo presence and cuckoo egg shape to detect parasitism.

Habitat selection in the lesser cuckoo, an avian brood parasite breeding on Jeju Island, Korea

BackgroundDetermining patterns of habitat use is key to understanding of animal ecology. Approximately 1% of bird species use brood parasitism for their breeding strategy, in which they exploit other species’ (hosts) parental care by laying eggs in their nests. Brood parasitism may complicate the habitat requirement of brood parasites because they need habitats that support both their host and their own conditions for breeding. Brood parasitism, through changes in reproductive roles of sex or individual, may further diversify habitat use patterns among individuals. However, patterns of habitat use in avian brood parasites have rarely been characterized. In this study, we categorized the habitat preference of a population of brood parasitic lesser cuckoos (Cuculus poliocephalus) breeding on Jeju Island, Korea. By using compositional analyses together with radio-tracking and land cover data, we determined patterns of habitat use and their sexual and diurnal differences.ResultsWe found that the lesser cuckoo had a relatively large home range and its overall habitat composition (the second-order selection) was similar to those of the study area; open areas such as the field and grassland habitats accounted for 80% of the home range. Nonetheless, their habitat, comprised of 2.54 different habitats per hectare, could be characterized as a mosaic. We also found sexual differences in habitat composition and selection in the core-use area of home ranges (third-order selection). In particular, the forest habitat was preferentially utilized by females, while underutilized by males. However, there was no diurnal change in the pattern of habitat use. Both sexes preferred field habitats at the second-order selection. At the third-order selection, males preferred field habitats followed by grasslands and females preferred grasslands followed by forest habitats.ConclusionsWe suggest that the field and grassland habitats represent the two most important areas for the lesser cuckoo on Jeju Island. Nevertheless, this study shows that habitat preference may differ between sexes, likely due to differences in sex roles, sex-based energy demands, and potential sexual conflict.

Female-female aggression and male responses to the two colour morphs of female common cuckoos

Female-only colour polymorphism is rare in birds, but occurs in brood parasitic cuckoos (Cuculidae). Obligate brood parasites leave incubation and parental care to other species (hosts), so female-female interactions can play a role in how parasites guard critical resources (host nests) within their laying areas. The plumage of adult female common cuckoos (Cuculus canorus) is either rufous (typically rare) or grey (common), whereas adult male conspecifics are monochromatic (grey). In previous studies, hosts and conspecific males responded with less intensity toward the rare female morph in support of a negative frequency-dependent benefit of female plumage polychromatism. Here, we assessed responses of both conspecific females and males to vocal playbacks of female calls, coupled with one of two 3D models of the different morphs of female cuckoos. At our study population, the rufous female morph was as common as the grey morph; therefore, we predicted similarly high rates of conspecific responses in both treatments. Both female and male cuckoos responded to playbacks acoustically, which demonstrated the primary role of acoustic communication in social interactions amongst cuckoos. Following this, some cuckoos flew closer to the models to inspect them visually. As predicted, no significant differences were detected between the live cuckoos’ responses toward the two colour morphs in this population. We conclude that dichromatism in female cuckoos evolved to serve one or more functions other than conspecific signalling.

Diet specialization and brood parasitism in cuckoo species.

Brood parasitism is a breeding strategy adopted by many species of cuckoos across the world. This breeding strategy influences the evolution of life histories of brood parasite species.In this study, we tested whether the degree on diet specialization is related to the breeding strategy in cuckoo species, by comparing brood parasite and nonparasite species. We measured the gradient of diet specialization of cuckoos, by calculating the Gini coefficient, an index of inequality, on the multiple traits describing the diet of species. The Gini coefficient is a measure of statistical dispersion on a scale between 0 and 1, reflecting a gradient from low to high specialization, respectively. First, we tested the strength of the phylogenetic signal of diet specialization index among cuckoo species worldwide. Then, we ran phylogenetic generalized least square (PGLS) models to compare diet specialization, distribution range, and body mass of parasitic and nonparasitic cuckoo species, considering the phylogenetic signal of data.After adjusting for the phylogenetic signal of the data and considering both, species distribution range and species body mass, brood parasitic cuckoos were characterized by higher diet specialization than nonbrood parasitic species. Brood parasitic species were also characterized by a larger breeding distribution range than nonparasitic species.The findings of this study provide an additional understanding of the cuckoos’ ecology, relating diet and breeding strategies, information that could be important in conservation ecology.

Novel instance of brood parasitic cuckoo nestlings using bright yellow patches to mimic gapes of host nestlings

Here we documented brood parasitism by the poorly studied Whistling Hawk-Cuckoo (Hierococcyx nisicolor) on the Rufous-bellied Niltava (Niltava sundara). We describe new information on egg size and incubation and nestling periods for Whistling Hawk-Cuckoo as well as a novel observation regarding cuckoo nestling and host interaction. Whistling Hawk-Cuckoo chicks displayed a vivid-colored gape when host parents were provisioning food. In addition, Whistling Hawk-Cuckoo chicks displayed bright yellow wing patches to their host parents. We observed that host parents tried to place food onto the wing-patch of the nestling instead of into its mouth. We suggest that chicks displaying such wing patches mimicking nestling gapes might be a common strategy for some brood parasite species of the genus Hierococcyx. This behavior also likely occurs in 2 other cuckoos in this genus, H. pectoralis and H. fugax. Finally, we suggest that the bright yellow uropygial gland of young nestlings might also function as an extra gape for the period when the young nestling is not capable of displaying the yellow wing patches.

Observations on the behaviour and ecology of the Pallid Cuckoo Heteroscenes pallidus in south-eastern Queensland

The Pallid Cuckoo Heteroscenes pallidus is a species of Old World brood-parasitic cuckoo (Tribe: Cuculini) that has received relatively little research attention, resulting in a lack of information on several aspects of its natural history. Over the course of c. 16 weeks (between September 2017 and January 2018), we recorded daily observations of at least six individuals present at the study site at Lake Samsonvale, Queensland. Here we present a summary of our observations including details on habitat preferences, plumages, vocalisations, social behaviour and interactions between Pallid Cuckoos and their potential hosts. We discuss these observations and suggest potential avenues for future research.

True recognition of nestlings by hosts selects for mimetic cuckoo chicks.

Brood parasitic cuckoos lay their eggs in other birds' nests, whereafter the young cuckoo hatches, ejects its nest-mates and monopolizes the care of the host parents. Theory predicts that hosts should not evolve to recognize and reject cuckoo chicks via imprinting because of the risk of mistakenly imprinting on a cuckoo chick in their first brood and thereafter always rejecting their own chicks. However, recent studies have revealed that some hosts do reject cuckoo chicks from the nest, indicating that these hosts' recognition systems either do not rely on first brood imprinting, or use cues that are independent of chick phenotype. Here, we investigate the proximate mechanisms of chick rejection behaviour in the large-billed gerygone (Gerygone magnirostris), a host of the little bronze-cuckoo (Chalcites minutillus). We find that gerygones use true template-based recognition based on at least one visual chick trait (the number of hatchling down-feathers), and that this is further mediated by experience of adult cuckoos at the nest during egg-laying. Given the theoretical constraints of acquiring recognition templates via imprinting, gerygones must possess a template of own-chick appearance that is largely innate. This true recognition has facilitated the evolution of very rapid hatchling rejection and, in turn, striking visual mimicry of host young by little bronze-cuckoo chicks.