Host Nestlings Research Articles

Brood parasitism and host-parasite relationships: Cuckoos adapt to reduce the time of hatching ahead of host nestlings by increasing egg thickness

The phenomenon of cuckoos’ brood parasitism is well known and can be investigated using applied mathematical techniques. Among adaptive features of this phenomenon are certain egg parameters that ensure their shortened incubation period (I) and thus the successful survival of their offspring. In particular, the volume of a cuckoo egg is not less than, or exceeds, that of the host species, which should, in theory, increase I. Also, cuckoo eggs have thicker shell than that of nest hosts. Here, we analyzed the available geometric dimensions of eggs in 447 species and found an inverse correlation (−0.585, p < 0.05) between I and the shell thickness-to-egg surface area ratio (T/S). A mathematical relationship was derived to calculate I depending on T/S. This premise was confirmed by comparative calculations using egg images of two parasitic species, common (Cuculus canorus) and plaintive cuckoo (Cacomantis merulinus) and their hosts: great reed warbler (Acrocephalus arundinaceus), European robin (Erithacus rubecula), rufescent prinia (Prinia rufescens), and common tailorbird (Orthotomus sutorius). An average calculated I value for cuckoo eggs was one day less than that for host eggs. Our findings unravel additional details of how cuckoos adapt to brood parasitism and specific host-parasite relationships.

Three sympatric host nestlings eavesdrop on cuckoo nestling distress calls.

In predator-prey interactions, the prey faces extreme challenges from predation, which drives the evolution of defense or anti-predator mechanisms. Compared with adult birds, nestlings are more vulnerable but not helpless. However, data on whether nestlings eavesdrop on the danger signals transmitted by other prey nestlings and the mechanisms of eavesdropping remain limited. In brood parasitism, common cuckoo (Cuculus canorus) nestlings, raised by host adults who are not closely related, offer an instructive system for studying the transmission and recognition of danger signals among nestlings of different species that share special relationships. We played back the distress calls of common cuckoo nestlings to nestlings of three sympatric host species (the oriental reed warbler Acrocephalus orientalis, which is a primary host of the common cuckoo, the reed parrotbill Paradoxornis heudei, an occasional host, and the vinous-throated parrotbill Sinosuthora webbiana, which is not parasitized in the study area) to investigate whether the host nestlings reduced their begging behavior. We also quantified the degree of inhibition toward begging behavior for these nestlings. The results revealed that, in response to the distress calls, the three sympatric host species markedly suppressed their begging behavior. This response can likely be attributed to the innate response of host nestlings caused by the general characteristics of distress calls, rather than the acoustic similarity and phylogenetic relationship between host nestlings and cuckoo nestlings. Furthermore, we observed that upon hearing the distress calls of cuckoo nestlings, the oriental reed warbler nestlings exhibited the greatest reduction in the total number of calls compared to the other two host species, potentially owing to stronger predation and parasitic pressures. This study suggests that host nestlings can detect danger signals emitted by parasitic nestlings; however, further investigation is needed to determine whether they can respond to distress calls from unfamiliar nestlings in different regions.

Host avian species and environmental conditions influence the microbial ecology of brood parasitic brown-headed cowbird nestlings: What rules the roost?

The role of species interactions, as well as genetic and environmental factors, all likely contribute to the composition and structure of the gut microbiome; however, disentangling these independent factors under field conditions represents a challenge for a functional understanding of gut microbial ecology. Avian brood parasites provide unique opportunities to investigate these questions, as brood parasitism results in parasite and host nestlings being raised in the same nest, by the same parents. Here we utilized obligate brood parasite brown-headed cowbird nestlings (BHCO; Molothrus ater) raised by several different host passerine species to better understand, via 16S rRNA sequencing, the microbial ecology of brood parasitism. First, we compared faecal microbial communities of prothonotary warbler nestlings (PROW; Protonotaria citrea) that were either parasitized or non-parasitized by BHCO and communities among BHCO nestlings from PROW nests. We found that parasitism by BHCO significantly altered both the community membership and community structure of the PROW nestling microbiota, perhaps due to the stressful nest environment generated by brood parasitism. In a second dataset, we compared faecal microbiotas from BHCO nestlings raised by six different host passerine species. Here, we found that the microbiota of BHCO nestlings was significantly influenced by the parental host species and the presence of an inter-specific nestmate. Thus, early rearing environment is important in determining the microbiota of brood parasite nestlings and their companion nestlings. Future work may aim to understand the functional effects of this microbiota variability on nestling performance and fitness.

Multiparasitism and repeated parasitism by the great spotted cuckoo Clamator glandarius on its main host, the magpie Pica pica: effects on reproductive success, nest desertion and nest predation

Brood parasites are expected to lay only one egg per parasitized nest, as the existence of several parasitic nestlings in a brood increases competition and can lead the starvation of some of them. However, multiparasitism (laying of two or more eggs by one or more parasitic females in a single host nest) is surprisingly frequent. Here, we study multiparasitism by different females or by the same female (repeated parasitism) in the great spotted cuckoo Clamator glandarius, a non‐evictor brood parasite that mainly parasitizes the magpie Pica pica, and whose chicks may be raised together with host nestlings in the same nest. We used a total of 262 magpie nests found during four breeding seasons. Multiparasitism and repeated parasitism are very frequent because this brood parasite is less virulent than other cuckoo species and magpie hosts can successfully raise more than one parasitic nestling per nest. The total number of cuckoo chicks fledged was higher in multiparasitized nests than in single‐ or double‐parasitized magpie nests. Magpie breeding success (i.e. the proportion of eggs that produce young that leave the nest) did not differ between single‐, double‐, and multiparasitized magpie nests. These results suggest that multiparasitism is an adaptation in the great spotted cuckoo. The intensity of parasitism (number of cuckoo eggs per nest), after controlling for the potential effect of year, did not affect nest desertion or nest predation rate, neither during the incubation nor the nestling periods. This implies that nest concealment does not affect the susceptibility of one nest being parasitized and predated, as nest predation rate was similar regardless of the intensity of parasitism. Predation rate during the nestling phase did not vary according to intensity of parasitism, which does not support either the ‘mutualism' hypothesis or the ‘predation cost of begging' hypothesis.

Polymorphism at the nestling stage and host-specific mimicry in an Australasian cuckoo-host arms race.

Decades of research have shown that the coevolutionary arms race between avian brood parasites and their hosts can promote phenotypic diversification in hosts and brood parasites. However, relatively little is known about the role of brood parasitism in promoting phenotypic diversification of nestlings. We review field data collected over four decades in Australia, New Caledonia and New Zealand to assess potential for coevolutionary interactions between the shining bronze-cuckoo (Chalcites lucidus) and its hosts, and how diversification at the nestling stage may be generating different subspecies. The shining bronze-cuckoo is a specialist parasite of a few hosts in the family Acanthizidae. It has diversified into subspecies, of which the nestlings closely mimic the respective host nestlings in each region. Additionally, some cuckoo subspecies have polymorphic nestlings. The Acanthizidae hosts have similar breeding and nesting habits and only moderately effective frontline defences against parasitism at cuckoo egg laying or at the egg stages. However, some hosts have developed highly effective defences at the nestling stage by recognising and ejecting cuckoo nestlings from the nest. As with the cuckoo nestlings, some hosts have polymorphic nestlings. The coevolutionary interactions in each region suggest different evolutionary stages of the arms race in which either the parasite or the host is currently in the lead. The presence of moderately effective defences at the egg laying and egg stages might explain why some hosts do not have defences at the nestling stage. The south-Pacific cuckoo - host systems are excellent models to explore the evolutionary mechanisms driving the diversification at the nestling stage in the coevolutionary arms race between avian brood parasites and their hosts.

Niche construction through a Goldilocks principle maximizes fitness for a nest-sharing brood parasite.

Generalist brood parasites that share nests with host nestlings can optimize resource acquisition from host parents by balancing the benefits that host nest-mates provide, including attracting increased provisions to the nest, against the costs of competing with the same host young over foster parental resources. However, it is unclear how parasitic chicks cope when faced with more nest-mates than are optimal for their survival upon hatching. We suggest that, in the obligate brood parasitic brown-headed cowbird (Molothrus ater), chicks use a niche construction strategy and reduce larger, more competitive host broods to maximize the parasites' survival to fledging. We experimentally altered brood sizes to test for Goldilocks principle patterns (i.e. a 'just right' intermediate brood size) of cowbird survival in nests of prothonotary warbler (Protonotaria citrea) hosts. We found that intermediate brood sizes of two host nestlings maximized cowbird fledging success relative to 0 or 4 host nest-mates at hatching. Specifically, cowbird nestlings lowered host brood sizes towards this optimum when placed in broods with more host nestlings. The results suggest that cowbirds reduce, but do not eliminate, host broods as a niche construction mechanism to improve their own probability of survival.

Common Cuckoo Nestling Adapts Its Begging Behavior to the Alarm Signaling System of a Host

Cuckoo nestlings thrive as avian brood parasites. To acquire sufficient food from the host parents, cuckoo nestlings generally make louder begging calls than host nestlings, but this may cause them to be more likely to attract the attention of predators. Studies have shown that nestlings would respond to the alarm calls of their parents by begging less, or crouching and remaining silent as an adaptation to reduce the risk of being heard by predators. Nevertheless, research is lacking on how parasite nestlings respond to alarm calls of their host parents. We studied the common cuckoo (Cuculus canorus) and one of the most common cuckoo host species, the oriental reed warbler (Acrocephalus orientalis), using a playback experiment in Yongnianwa National Wetland Park during the breeding seasons from June to July, 2020–2021. The begging behaviors of either cuckoo or host nestlings were quantified by playing back the alarm calls of host adults toward common cuckoo, sparrowhawk (Accipiter nisus), or oriental turtle doves (Streptopelia orientalis). Meanwhile, normal begging without playback, playback of the natural singing (NS) of host adults, and background noise (BN) were included as behavioral reference, non-threatening comparison, and playback control, respectively. The results showed that the cuckoo and host nestlings produced similar levels of begging with or without playback of NS and BN; however, both types of nestlings inhibited their begging intensity after hearing the playback of alarm calls, although they did not respond differently to the various alarm call playbacks. This study therefore elucidated that coevolution has selected the common cuckoo nestlings that adapt their begging behavior to the parent–offspring communication of alarm signaling in their host, oriental reed warblers.

Discrimination and ejection of eggs and nestlings by the fan-tailed gerygone from New Caledonia.

Nestling rejection is a rare type of host defense against brood parasitism compared with egg rejection. Theoretically, host defenses at both egg and nestling stages could be based on similar underlying discrimination mechanisms but, due to the rarity of nestling rejector hosts, few studies have actually tested this hypothesis. We investigated egg and nestling discrimination by the fan-tailed gerygone Gerygone flavolateralis, a host that seemingly accepts nonmimetic eggs of its parasite, the shining bronze-cuckoo Chalcites lucidus, but ejects mimetic parasite nestlings. We introduced artificial eggs or nestlings and foreign gerygone nestlings in gerygone nests and compared begging calls of parasite and host nestlings. We found that the gerygone ejected artificial eggs only if their size was smaller than the parasite or host eggs. Ejection of artificial nestlings did not depend on whether their color matched that of the brood. The frequency of ejection increased during the course of the breeding season mirroring the increase in ejection frequency of parasite nestlings by the host. Cross-fostered gerygone nestlings were frequently ejected when lacking natal down and when introduced in the nest before hatching of the foster brood, but only occasionally when they did not match the color of the foster brood. Begging calls differed significantly between parasite and host nestlings throughout the nestling period. Our results suggest that the fan-tailed gerygone accepts eggs within the size range of gerygone and cuckoo eggs and that nestling discrimination is based on auditory and visual cues other than skin color. This highlights the importance of using a combined approach to study discrimination mechanisms of hosts.

The effect of avian brood parasitism on physiological responses of host nestlings.

Avian obligate brood parasites lay their eggs in the nests of other species that may provide care for the foreign offspring. Brood parasitism often imparts substantial fitness losses upon host nestlings when they are raised alongside the typically more competitive, larger, and older parasitic chick(s). Whereas fitness costs due to reduced host offspring survival in parasitized broods have been studied in detail, the physiological changes in host nestlings caused by parasitic nestmate(s) are less well known. We compared prothonotary warbler (Protonotaria citrea) nestlings, a host of the nest-sharing brown-headed cowbird (Molothrus ater), in experimentally parasitized vs. non-parasitized broods. Our aim was to determine whether cohabitation with brood parasitic young impacted host nestling baseline corticosterone plasma concentrations, immune responses, body condition, and mortality. Corticosterone levels and body condition of host nestlings were similar between nests with or without a cowbird nestmate, whereas host immune responses were lower and nestling mortality was greater in parasitized broods, irrespective of variation in brood size or total brood mass. We detected no trade-offs of baseline corticosterone levels with either immune responses or with body condition. These results suggest that this host species' nestlings experience some adverse fitness-relevant physiological effects in parasitized broods, but are also resilient in other aspects when coping with brood parasitism.

Killing behaviour of adult brood parasites

Abstract Decades of studies have revealed the striking adaptations of avian brood parasites for their unique reproductive lifestyle. Several have reported that adult brood parasites sometimes kill host nestlings, although the reasons for this behaviour remain unclear. Using continuous video-recording and camera traps, we observed the same behaviour in the common cuckoo Cuculus canorus, showing that both host and parasite nestlings can be killed. The latter has never previously been observed in cuckoos. Here, we review this phenomenon and discuss possible explanations.

Multimodal mimicry of hosts in a radiation of parasitic finches.

Brood parasites use the parental care of others to raise their young and sometimes employ mimicry to dupe their hosts. The brood-parasitic finches of the genus Vidua are a textbook example of the role of imprinting in sympatric speciation. Sympatric speciation is thought to occur in Vidua because their mating traits and host preferences are strongly influenced by their early host environment. However, this alone may not be sufficient to isolate parasite lineages, and divergent ecological adaptations may also be required to prevent hybridization collapsing incipient species. Using pattern recognition software and classification models, we provide quantitative evidence that Vidua exhibit specialist mimicry of their grassfinch hosts, matching the patterns, colors and sounds of their respective host's nestlings. We also provide qualitative evidence of mimicry in postural components of Vidua begging. Quantitative comparisons reveal small discrepancies between parasite and host phenotypes, with parasites sometimes exaggerating their host's traits. Our results support the hypothesis that behavioral imprinting on hosts has not only enabled the origin of new Vidua species, but also set the stage for the evolution of host-specific, ecological adaptations.

The gut microbiota of brood parasite and host nestlings reared within the same environment: disentangling genetic and environmental effects.

Gut microbiota are essential for host health and survival, but we are still far from understanding the processes involved in shaping their composition and evolution. Controlled experimental work under lab conditions as well as human studies pointed at environmental factors (i.e., diet) as the main determinant of the microbiota with little evidence of genetic effects, while comparative interspecific studies detected significant phylogenetic effects. Different species, however, also differ in diet, feeding behavior, and environmental characteristics of habitats, all of which also vary interspecifically, and, therefore, can potentially explain most of the detected phylogenetic patterns. Here, we take advantage of the reproductive strategy of avian brood parasites and investigate gut microbiotas (esophageal (food and saliva) and intestinal) of great spotted cuckoo (Clamator glandarius) and magpie (Pica pica) nestlings that grow in the same nests. We also estimated diet received by each nestling and explored its association with gut microbiota characteristics. Although esophageal microbiota of magpies and great spotted cuckoos raised within the same environment (nest) did not vary, the microbiota of cloacal samples showed clear interspecific differences. Moreover, diet of great spotted cuckoo and magpie nestlings explained the microbiota composition of esophageal samples, but not of cloaca samples. These results strongly suggest a genetic component determining the intestinal microbiota of host and parasitic bird species, indicating that interspecific differences in gut morphology and physiology are responsible for such interspecific differences.

Nestlings of the common cuckoo do not mimic begging calls of two closely related Acrocephalus hosts

Nestlings of the obligate brood-parasitic common cuckoo, Cuculus canorus, use diverse signals to manipulate host parents into feeding them. Begging calls, one of the most prominent parent–offspring communication signals, have been suggested to differ between cuckoos parasitizing different host species but the call characteristics involved differ between studies. We studied nestling begging calls of the cuckoo and two closely related cuckoo hosts breeding in sympatry, the great reed warbler, Acrocephalus arundinaceus, and the reed warbler, Acrocephalus scirpaceus, to determine whether cuckoo nestlings adjust their begging calls according to the host species and if these calls vary with cuckoo age and sex. We found that begging calls of host nestlings differed markedly between species but there was no difference in the begging calls of cuckoo nestlings raised by great reed warblers and those raised by reed warblers. These results suggest that cuckoo nestlings do not adjust begging vocalizations to match host species but rather use general begging call features to solicit food. However, their call frequency band narrowed, syllable duration shortened and call rate tended to increase with increasing age. None of the begging call characteristics differed between the sexes. The rapid development of cuckoo begging call parameters during ontogeny suggests that any comparisons of begging calls of cuckoo nestlings raised by different host species must control for nestling age. Finally, some discordant conclusions of this and other studies emphasize how little we understand parasite–host communication.

Brood parasitic nestlings benefit from unusual host defenses against botfly larvae (Philornis spp.)

Brood parasitic birds lay their eggs into the nests of other birds, abandoning parental care of their nestlings to the unsuspecting hosts. Parasite and host nestlings may themselves be parasitized by botfly larvae (Philornis: Muscidae), which burrow under the nestlings’ skin and can seriously affect growth and survival. Here, we provide the first direct evidence that adult baywings (Agelaioides badius), the primary host of the specialist brood parasitic screaming cowbird (Molothrus rufoaxillaris), regularly remove botfly larvae from their own and parasitic nestlings by pulling them out of the nestlings’ skin. This is the only bird species known to remove botfly larvae. By combining nestling cross-fostering with video recording of baywing nests, we show that due to prompt removal, infection with botfly larvae had negligible effects on nestling growth and survival despite high prevalence. Our results provide the first direct observations for larva removal behavior in botfly hosts. Screaming cowbirds may benefit from using baywings as its main host, as larva removal by adult baywings reduces the costs of botfly parasitism. Infection by botfly larvae of the genus Philornis (Muscidae) causes nestling mortality in many Neotropical birds. Despite the lethal effects, most Philornis hosts studied so far lack specific defenses against these larvae. The grayish baywing (Agelaioides badius), primary host of the brood parasitic screaming cowbird (Molothrus rufoaxillaris), is the only species that, based on indirect evidence, would be able to remove Philornis larvae from infected nestlings. We provide the first direct evidence that adult baywings do indeed remove botfly larvae from their own nestlings as well as from parasitic cowbird nestlings and that this unusual defense may increase the survival of own and screaming cowbird nestlings at infected nests.

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.

Non-mimetic shiny cowbird nestlings escape discrimination by baywings in absence of host nest mates

Nestlings of obligate brood parasites must obtain resources from heterospecific hosts that are attuned to the solicitation behaviours of their own progeny. Failing to match the appropriate stimuli may result in suboptimal provisioning or even the starvation of parasite young. Parasitic nestlings could overcome it by sharing the nest with host young, as long as they are able to compete efficiently for parental feedings. Here, we examined if non-mimetic shiny cowbird (Molothrus bonariensis) nestlings reared alone fail to elicit sufficient parental care from the grayish baywing (Agelaioides badius), a host that discriminates between their own and parasitic nestlings based on species-specific begging cues. We manipulated baywing broods to assess the ability of shiny cowbird nestlings to elicit parental provisioning and survive without host nest mates. Host provisioning rates and survival did not differ between shiny cowbirds reared alone and host nestlings in singleton broods. Also, growth patterns of experimental nestlings reared alone were similar to those reported for shiny cowbirds reared alongside baywing young. Hence, we did not find support for the hypothesis that non-mimetic nestlings require the assistance of host nest mates to elicit sufficient parental care from its baywing host. Furthermore, we found that shiny cowbirds that were reared alone continued receiving care from baywings after fledging, unlike shiny cowbirds from mixed broods. Our results add evidence to the idea of opposing selective pressures on the evolution of nest mate acceptance in cowbirds and suggest context-dependent host’s discrimination abilities that deserve further investigation. The evolution of nest mate killing versus tolerance strategies is a long-standing question in the study of brood parasitism. Parasitic nestlings may benefit from sharing the nest with host young if they collectively induce more parental provisioning and the parasite can benefit from it. Host nest mates could also confer protection against discrimination when hosts respond preferentially to stimuli of their own kind. We examined this idea in a generalist brood parasite, the shiny cowbird (Molothrus bonariensis), and a host able to discriminate species-specific begging cues. The results showed that shiny cowbirds reared alone performed well and circumvent host discrimination also after leaving the nest. Our study supports the existence of trade-offs on the evolution of nest mate killing behaviours and adds evidence that context-dependent host’s discrimination abilities similar to those observed towards parasitic eggs can be at play towards parasitic fledglings.

Development and behavior of Plaintive Cuckoo (Cacomantis merulinus) nestlings and their Common Tailorbird (Orthotomus sutorius) hosts

BackgroundOur knowledge of avian brood parasitism is primarily based on studies of a few selected species. Recently, researchers have targeted a wider range of host–parasite systems, which has allowed further evaluation of hypotheses derived from well-known study systems but also disclosed adaptations that were previously unknown. Here we present developmental and behavioral data on the previously undescribed Plaintive Cuckoo (Cacomantis merulinus) nestling and one of its hosts, the Common Tailorbird (Orthotomus sutorius).MethodsWe discovered more than 80 Common Tailorbird nests within an area of 25 km2, and we recorded nestling characteristics, body mass, tarsus length and begging display every 3 days for both species.ResultsPlaintive Cuckoo nestlings followed a developmental pathway that was relatively similar to that of their well-studied relative, the Common Cuckoo (Cuculus canorus). Tailorbird foster siblings were evicted from the nest rim. The cuckoo nestlings gained weight faster than host nestlings, and required 3–9 days longer time to fledge than host nestlings. Predation was high during the early stages of development, but the nestlings acquired a warning display around 11 days in the nest, after which none of the studied cuckoo nestlings were depredated. The cuckoos’ begging display, which appeared more intense than that of host nestlings, was initially vocally similar with that of the host nestlings but began to diverge from the host sound output after day 9.ConclusionsThe developmental data on Plaintive Cuckoo nestlings and their tailorbird host builds an important foundation for future work on the co-evolutionary interactions in this parasite–host system.

Innate development of acoustic signals for host parent–offspring recognition in the brood‐parasitic Screaming CowbirdMolothrus rufoaxillaris

Young birds communicate their need to parents through complex begging displays that include visual and acoustic cues. Nestlings of interspecific brood parasites must ‘tune’ into these communication channels to secure parental care from their hosts. Various studies show that parasitic nestlings can effectively manipulate host parental behaviour through their begging calls, but how these manipulative acoustic signals develop in growing parasites remains poorly understood. We investigated the influence of social experience on begging call development in a host‐specialist brood parasite, the Screaming CowbirdMolothrus rufoaxillaris. Screaming Cowbird nestlings look and sound similar to those of the primary host, the Greyish BaywingAgelaioides badius. This resemblance is likely to be adaptive because Baywings discriminate against fledglings unlike their own and provision nests at higher rates in response to Baywing‐like begging calls than to non‐mimetic begging calls. By means of cross‐fostering and playback experiments, we tested whether the acoustic cues that elicit recognition by Baywings develop innately in Screaming Cowbird nestlings or are acquired through social experience with host parents or nest mates. Our results suggest that begging call structure was partially modulated by experience because Baywing‐reared Screaming Cowbird and host nestlings were acoustically more similar as age increased, whereas acoustic similarity between cross‐fostered and Baywing‐reared Screaming Cowbird nestlings decreased from 4–5 to 8–10 days of age. Cross‐fostered Screaming Cowbirds developed begging calls of lower minimum frequency and broader bandwidth than those of Baywing‐reared Screaming Cowbirds by the age of 8–10 days. Despite the observed differences in begging call structure, however, adult Baywings responded similarly to begging calls of 8‐ to 10‐day‐old cross‐fostered and Baywing‐reared Screaming Cowbirds, suggesting that these were functionally equivalent from the host's perspective. These findings support the idea that, although rearing environment can influence certain begging call parameters, the acoustic cues that serve for offspring recognition by Baywings develop in young Screaming Cowbirds independently of social experience.

Breeding biology of the Fan-tailed Gerygone Gerygone flavolateralis in relation to parasitism by the Shining Bronze-cuckoo Chalcites lucidus

Apart from a few well-studied examples, there is little information regarding the life history and ecological requirements of brood parasites and their hosts in most cuckoo–host systems, particularly in tropical areas. In New Caledonia, the Fan-tailed Gerygone Gerygone flavolateralis, is the exclusive host of the Shining Bronze-cuckoo, Chalcites lucidus. Here, the arms race has escalated to the nestling stage, and both host and parasite have polymorphic (difference in skin coloration) nestlings. This is a novel system for the study of brood parasitism, but very little is known about the breeding biology of the Fan-tailed Gerygone and how this may affect the co-evolutionary interactions with the Shining Bronze-cuckoo. We monitored active nests of the Fan-tailed Gerygone during six breeding seasons, using video monitoring and direct observation. Nest attendance periods of host parents were shorter during laying than during incubation, and therefore parasitism was more likely to occur during the laying period. Cuckoos eggs were on average 2 days more developed than host eggs, and thus cuckoo nestlings usually hatched before host nestlings. Fan-tailed Gerygone nestling phenotypes had similar growth and fledging rates and their frequency did not differ between habitats, indicating no apparent trade-off with skin coloration. The precipitation regime affected predation but not the parasitism rate. The current situation in New Caledonia suggests a higher selection pressure on the parasite than on the host. Our study highlights the importance of data on the breeding biology of the host in the context of studies on brood parasitism.

Visual discrimination of polymorphic nestlings in a cuckoo-host system

Mimicry by avian brood parasites favours uniformity over variation within a breeding attempt as host defence against parasitism. In a cuckoo-host system from New Caledonia, the arms race resulted in both host (Gerygone flavolateralis) and parasite (Chalcites lucidus) having nestlings of two discrete skin colour phenotypes, bright and dark. In our study sites, host nestlings occurred in monomorphic and polymorphic broods, whereas cuckoo nestlings only occurred in the bright morph. Irrespective of their brood colour, host parents recognised and ejected parasite nestlings but never ejected their own. We investigated whether host parents visually recognised their own nestlings by using colour, luminance and pattern of multiple body regions. We found that the parasite mimicked multiple visual features of both host morphs and that the visual difference between host morphs was larger than the difference between the parasite and the mimicked host morph. Visual discrimination alone may result in higher chances of recognition errors in polymorphic than in monomorphic host broods. Host parents may rely on additional sensorial cues, not only visual, to assess nestling identity. Nestling polymorphism may be a trace of evolutionary past and may only have a marginal role in true-recognition of nestlings in the arms race in New Caledonia.