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1.
In recent decades, numerous studies have examined factors affecting risk of host nest parasitism in well‐known avian host–parasite systems; however, little attention has been paid to the role of host nest availability. In accordance with other studies, we found that nest visibility, reed density and timing of breeding predicted brood parasitism of Great Reed Warblers Acrocephalus arundinaceus by the Common Cuckoo Cuculus canorus. More interestingly, hosts had a greater chance of escaping brood parasitism if nesting was synchronized. Cuckoo nest searching was governed primarily by nest visibility at high host‐nest density. However, even well‐concealed nests were likely to be parasitized during periods when just a few hosts were laying eggs, suggesting that Cuckoos adjust their nest‐searching strategy in relation to the availability of host nests. Our results demonstrate that host vulnerability to brood parasitism varies temporally and that Cuckoo females are able to optimize their nest‐searching strategy. Moreover, our study indicated that Cuckoos always manage to find at least some nests to parasitize. Thus, in this case, the co‐evolutionary arms race should take place mainly in the form of parasitic egg rejection rather than via frontline pre‐parasitism defence.  相似文献   

2.
In the arms race between avian brood parasites and their hosts, several adaptations and counter‐adaptations have evolved. The most prominent host defence is rejection of parasitic eggs. We experimentally parasitized nests of 10 potential host species breeding in sympatry with four different cuckoo species in an area in Bangladesh using differently coloured model eggs to test host responses. In four species we introduced both mimetic and non‐mimetic eggs. Black Drongos Dicrurus macrocercus, hosts of the Indian Cuckoo Cuculus micropterus, rejected all model eggs. Common Mynas Acridotheres tristis and Jungle Babblers Turdoides striata accepted all eggs regardless of mimicry. These two species are parasitized by Asian Koels Eudynamys scolopaceus, Common Hawk‐cuckoo Hierococcyx varius and, in the case of Jungle Babblers, Jacobin Cuckoos Clamator jacobinus. Pied Mynas Gracupica contra, with no records of parasitism in our study area, also accepted all eggs regardless of mimicry. In the six remaining species, all of which lay spotted eggs, we introduced only non‐mimetic eggs. Black‐hooded Orioles Oriolus xanthornus rejected all model eggs, even though we have found no records of natural parasitism. Long‐tailed Shrikes Lanius schach and House Crows Corvus splendens, hosts of Asian Koels, rejected 75 and 9.1% of model eggs, respectively. Large‐billed Crows Corvus macrorhynchos, apparently not used as hosts in our study area, accepted all blue but rejected all brown model eggs. Oriental Magpie‐Robins Copsychus saularis and Red‐vented Bulbuls Pycnonotus cafer accepted all non‐mimetic model eggs. In Black Drongos, Long‐tailed Shrikes and Black‐hooded Orioles, all model eggs were ejected within 24 h of introduction. The results show considerable variation in egg rejection rates among various species, providing baseline data for further investigation of co‐evolutionary interactions between brood parasites and hosts in this region.  相似文献   

3.
Three species of brood parasites are increasingly being recorded as transoceanic vagrants in the Northern Hemisphere, including two Cuculus cuckoos from Asia to North America and a Molothrus cowbird from North America to Eurasia. Vagrancy patterns suggest that their establishment on new continents is feasible, possibly as a consequence of recent range increases in response to a warming climate. The impacts of invasive brood parasites are predicted to differ between continents because many host species of cowbirds in North America lack egg rejection defenses against native and presumably also against invasive parasites, whereas many hosts of Eurasian cuckoos frequently reject non‐mimetic, and even some mimetic, parasitic eggs from their nests. During the 2014 breeding season, we tested the responses of native egg‐rejecter songbirds to model eggs matching in size and color the eggs of two potentially invasive brood parasites. American Robins (Turdus migratorius) are among the few rejecters of the eggs of Brown‐headed Cowbirds (M. ater), sympatric brood parasites. In our experiments, robins rejected one type of model eggs of a Common Cuckoo (C. canorus) host‐race, but accepted model eggs of a second cuckoo host‐race as well as robin‐mimetic control eggs. Common Redstarts (Phoenicurus phoenicurus), frequent hosts of Common Cuckoos in Eurasia, rejected ~50% of model Brown‐headed Cowbird eggs and accepted most redstart‐mimetic control eggs. Our results suggest that even though some hosts have evolved egg‐rejection defenses against native brood parasites, the invasion of brood parasites into new continents may negatively impact both naïve accepter and coevolved rejecter songbirds in the Northern Hemisphere.  相似文献   

4.
Dozens of studies have documented that brood parasites are well adapted to a brood parasitic lifestyle but not all parasitism events are successful. Co-evolution between brood parasites and their hosts is a dynamic process so it is reasonable to expect that a female brood parasite may commit errors during egg deposition by laying her eggs outside the laying period of the host, with consequent impacts on her fitness. Using an extensive dataset from a long-term study, we evaluated egg-laying patterns and errors related to the timing of egg-laying in the Common Cuckoo Cuculus canorus (hereafter ‘Cuckoo’). Specifically, we tested whether the Cuckoo avoids laying before or on the day of host clutch initiation to reduce the risk of rejection of parasitic eggs, whether laying errors will be more frequent in periods with a lack of active host nests, and whether the laying errors will be more frequent in periods with intense Cuckoo parasitism and a consequent lack of suitable host nests. We found that about one-third of Cuckoo eggs were laid on the host clutch initiation day or 1 day before, and the percentage of Cuckoo eggs laid decreased thereafter. Surprisingly, the probability of Cuckoo egg acceptance by the hosts was not affected by the egg-laying stage of the host clutch. Errors in the timing of egg-laying with fatal consequences (i.e. those precluding Cuckoo hatching because of laying in incubated or deserted clutches) were recorded in about 5% of cases. Only laying date of a Cuckoo egg had a significant effect on the probability of errors, which increased during the breeding season. This may be related to the higher number of deserted and incubated host nests at the site at the end of the breeding season. Errors in egg-laying may be attributed to young and inexperienced females but also impaired body condition or intraspecific competition may cause this behaviour. Future studies, which will test these possible explanations, will help to understand better the mechanism of co-evolutionary arms races and differences between host specialist and generalist brood parasites in various host–parasite systems.  相似文献   

5.
We documented brood parasitism by the poorly studied Large Hawk‐Cuckoo on a previously unknown host species, the Chinese Babax. Furthermore, we describe a new egg colour for the Large Hawk‐Cuckoo. The parasitism rate of Chinese Babax nests over 4 years was 6.9% (11 of 159 nests), with significant temporal variation. The Large Hawk‐Cuckoo laid immaculate white eggs that appeared non‐mimetic to the blue Babax eggs, an impression that was confirmed by avian visual modelling. Nevertheless, most Cuckoo eggs were accepted by the host, suggesting that this host–parasite system may be evolutionarily recent.  相似文献   

6.
Two main mechanisms of egg rejection, the main defence of hosts against brood parasites, have been described: ejection and desertion. Desertion of the parasitized nest is much more costly and is usually exhibited by small‐sized host species unable to remove the parasitic egg. However, nest desertion is frequently assumed to be an anti‐parasite strategy even in medium or large‐sized host species. This assumption should be considered with caution because: 1) large‐sized hosts able to eject the parasitic egg should eject it rather than desert the nest, and 2) breeding birds may desert their nests in response to different disturbances other than brood parasitism. This problem is especially important in the common blackbird Turdus merula because this is a medium‐sized species, potential host of the common cuckoo Cuculus canorus, in which desertion has been frequently reported as a response to cuckoo egg models. Here, we seek to determine whether nest desertion can be considered a response unequivocally directed to the parasitic egg in medium‐sized hosts using the blackbird as the study species. In an experimental study in which we have manipulated levels of mimicry and size of experimental eggs, we have found that both colour (mimetic and non‐mimetic; at least for human vision) and size (small, medium, and large) significantly affected ejection rates but not nest desertion rates. In fact, although large eggs disproportionally provoked nest desertion more frequently than did small or medium‐sized eggs, cuckoo‐sized parasitic eggs were not deserted allowing us to conclude that desertion is unlikely to be an adaptive response to brood parasitism at least for this species.  相似文献   

7.
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.  相似文献   

8.
Brood parasite – host systems continue to offer insights into species coevolution. A notable system is the redstart Phoenicurus phoenicurus parasitized by the ‘redstart‐cuckoo’ Cuculus canorus gens. Redstarts are the only regular cuckoo hosts that breed in cavities, which challenges adult cuckoos in egg laying and cuckoo chicks in host eviction. We investigated parasitism in this system and found high overall parasitism rates (31.1% of 360 redstart nests), but also that only 33.1% of parasitism events (49 of 148 eggs) were successful in laying eggs into redstart nest cups. The majority of cuckoo eggs were mislaid and found on the rim of the nest; outside the nest cup. All available evidence suggests these eggs were not ejected by hosts. The effective parasitism rate was therefore only 12.8% of redstart nests. Redstarts responded to natural parasitism by deserting their nests in 13.0% of cases, compared to desertion rates of 2.8% for non‐parasitized nests. Our egg parasitism experiments found low rates (12.2%) of rejection of artificial non‐mimetic cuckoo eggs. Artificial mimetic and real cuckoo eggs added to nests were rejected at even lower rates, and were always rejected via desertion. Under natural conditions, only 21 cuckoo chicks fledged of 150 cuckoo eggs laid. Adding to this low success, is that cuckoo chicks are sometimes unable to evict all host young, and were more likely to die as a result compared to cuckoo chicks reared alone. This low success seems to be mainly due to the cavity nesting strategy of the redstart which is a challenging obstacle for the cuckoo. The redstart‐cuckoo system appears to be a fruitful model system and we suggest much more emphasis should be placed on frontline defences such as nest site selection strategies when investigating brood parasite–host coevolution.  相似文献   

9.
Most theoretical models of coevolution between brood parasites, whether interspecific or conspecific, and their hosts explicitly assume consistent individual behaviour in host egg‐rejection responses. Accordingly, hosts cast as acceptors always accept, whereas ejectors always reject parasitic eggs when exposed to stable ecological conditions. To date, only few studies have attempted to test this critical assumption of individual repeatability in egg‐rejection responses of hosts. Here, we studied the repeatability of egg rejection in blackbirds (Turdus merula) and song thrush (T. philomelos), species in which females are reported to reject simulated, non‐mimetic foreign eggs at intermediate frequencies at the population level. However, intermediate rates of acceptance and rejection can be consistent with either or both intra‐ and interindividual variability in rejection behaviours. Our experiments revealed generally high individual consistency in these hosts’ responses to experimentally introduced non‐mimetic and mimetic model foreign eggs. Individuals also responded faster on average to second than to first trials within the same breeding attempts, but the difference was statistically significant only in blackbirds. These results are consistent with the critical assumption of co‐evolutionary models, that statistically egg rejection is mostly individually repeatable, but also reveal that some individuals in both species change their responses even within the short time‐window of one breeding attempt. The data suggest that individuals reject foreign eggs faster when perceived parasitism risk is greater because of repeated introductions of experimental parasitic eggs. We provide methodological recommendations to facilitate experimental and meta‐analytical studies of individual egg rejection repeatability and discuss how to reduce technical constraints arising from disparate treatments and variable sample sizes for future studies.  相似文献   

10.
Brood parasites rely entirely on the parental care of host species to raise the parasitic nestlings until independence. The reproductive success of avian brood parasites depends on finding host nests at a suitable stage (i.e. during egg laying) for parasitism and weakly defensive (i.e. non‐ejector) hosts. Finding appropriate nests for parasitism may, however, vary depending on ecological conditions, including parasite abundance in the area, which also varies from one year to another and therefore may influence coevolutionary relationships between brood parasites and their hosts. In this scenario, we explored: 1) the degree of laying synchronization between great spotted cuckoos Clamator glandarius and magpies Pica pica during two breeding seasons, which varied in the level of selection pressure due to brood parasitism (i.e. parasitism rate); 2) magpie responses to natural parasitism in the pre‐laying period and successfulness of parasitic eggs laid at this stage; and 3) magpie responses to experimental parasitism performed at different breeding stages. We found that, during the year of higher parasitism rate, there was an increase in the percentage of parasitic eggs laid before magpies started laying. However, the synchronization of laying was poor both years regardless of the differences in the parasitism rate. The ejection rate was significantly higher during the pre‐egg‐laying and the post‐hatching stages than during the laying stage, and hatching success of parasitic eggs laid during the pre‐egg‐laying stage was zero. Thus, non‐synchronized parasitic eggs are wasted and therefore poor synchronization should be penalized by natural selection. We discuss four different hypotheses explaining poor synchronization.  相似文献   

11.
Avian hosts of brood parasites can evolve anti‐parasitic defenses to recognize and reject foreign eggs from their nests. Theory predicts that higher inter‐clutch and lower intra‐clutch variation in egg appearance facilitates hosts to detect parasitic eggs as egg‐rejection mainly depends on the appearance of the egg. Therefore, we predict that egg patterns and rejection rates will differ when hosts face different intensity of cuckoo parasitism. We tested this prediction in two populations of the plain prinia Prinia inornata: Guangxi in mainland China with high diversity and density of cuckoo species, and Taiwan where there is only one breeding cuckoo species, the oriental cuckoo Cuculus optatus. As expected, egg patterns were similar within clutches but different among clutches (polymorphic eggs) in the mainland population, while the island population produced more uniform egg morphs. Furthermore, the mainland population showed a high rate of egg rejection, while the island population exhibited dramatically reduced egg grasp‐rejection ability in the absence of parasitism by the common cuckoo Cuculus canorus. Our study suggests that prinias show lower intra‐clutch consistency in egg colour and lose egg‐rejecting ability under relaxed selection pressure from brood parasitism.  相似文献   

12.
Avian brood parasites lay their eggs in the nests of their hosts, which rear the parasite's progeny. The costs of parasitism have selected for the evolution of defence strategies in many host species. Most research has focused on resistance strategies, where hosts minimize the number of successful parasitism events using defences such as mobbing of adult brood parasites or rejection of parasite eggs. However, many hosts do not exhibit resistance. Here we explore why some hosts accept parasite eggs in their nests and how this is related to the virulence of the parasite. We also explore the extent to which acceptance of parasites can be explained by the evolution of tolerance; a strategy in which the host accepts the parasite but adjusts its life history or other traits to minimize the costs of parasitism. We review examples of tolerance in hosts of brood parasites (such as modifications to clutch size and multi‐broodedness), and utilize the literature on host–pathogen interactions and plant herbivory to analyse the prevalence of each type of defence (tolerance or resistance) and their evolution. We conclude that (i) the interactions between brood parasites and their hosts provide a highly tractable system for studying the evolution of tolerance, (ii) studies of host defences against brood parasites should investigate both resistance and tolerance, and (iii) tolerance and resistance can lead to contrasting evolutionary scenarios.  相似文献   

13.
In the continuing arms race between hosts and brood parasites, hosts are expected to reduce variation in the appearance of their own eggs within clutches, as it facilitates recognition of parasitic eggs. At the same time, by increasing interclutch variation, hosts should make it more difficult for parasites to evolve perfectly mimetic eggs. In this study, we experimentally manipulated intraclutch variation in the great reed warbler, Acrocephalus arundinaceus, in Hungary, where this species is heavily (c. 64%) parasitized by the common cuckoo, Cuculus canorus. We placed artificial cuckoo eggs, which appeared moderately mimetic to humans, in two groups of nests; in one group we increased variability of egg appearance within clutches by exchanging host eggs among nests. These clutches showed a significantly higher intraclutch variability than natural clutches, which we used as a control group. Our results indicate that it has no effect on rejection behaviour in this species, neither when variation was increased experimentally, nor within the natural range of variation displayed by our population. We suggest that when parasitism is high, selection for reduced intraclutch variation may be less important than frequency‐dependent selection for increased variation between individuals within a host population.  相似文献   

14.
Recent evidence suggests that blue‐green coloration of bird eggshells may be related to female and/or egg phenotypic quality, and that such colour may affect parental effort and therefore the nutritional environment of developing nestlings. Here we suggest that these relationships and the signal function of eggshell coloration would affect the outcome of coevolution between avian brood parasites and their hosts in at least three different non‐exclusive evolutionary pathways. First, by laying blue‐green coloured eggs, cuckoo females may exploit possible sensory biases of their hosts, constraining the evolution of parasitic egg recognition, and thus avoid rejection. Second, because of the relatively high costs of laying blue eggs, cuckoo females may be limited in their ability to mimic costly blue‐green eggs of their hosts because cuckoo females lay many more eggs than their hosts. Furthermore, costs associated with foreign egg recognition errors would be relatively higher for hosts laying blue eggs. Third, cuckoos may use coloration of host eggs for selecting individuals or specific hosts of appropriate phenotypic quality (i.e. parental abilities). We here explored some predictions emerging from the above scenarios and found partial support for two of them by studying egg coloration of European cuckoos (Cuculus canorus) and that of their 25 main hosts, as well as parasitism and rejection rate of hosts. Cuckoo hosts parasitized with more blue, green, and ultraviolet cuckoo eggs, or those laying more blue‐green eggs, were more prone to accept experimental parasitism with artificial cuckoo eggs. In addition, coloration of cuckoo eggs is more variable when parasitizing hosts laying bluer‐greener eggs, even after controlling for the effect of host egg coloration (i.e. degree of egg matching). Globally, our results are consistent with the proposed hypothesis that host egg traits that are related to phenotypic quality of hosts, such as egg coloration, may have important implications for the coevolutionary interaction between hosts and brood parasites. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, 106 , 154–168.  相似文献   

15.
Birds are capable of seeing the ultraviolet light (UV) spectrum and as a consequence have evolved UV‐reflective structures with signalling functions. Avian eggs also reflect in the UV spectrum but the importance of UV egg matching in egg rejection decisions has been equivocal. Here we conducted egg rejection experiments in the congeneric and sympatrically breeding Yellow‐bellied Prinia Prinia flaviventris and Plain Prinia Prinia inornata in Taiwan to assess the role of UV as a cue in egg discrimination. Yellow‐bellied Prinia is a host of Oriental Cuckoo Cuculus optatus, whereas Plain Prinia is not. We coated one prinia egg in the experimental clutches with a cream containing a UV‐blocking agent, while the rest of the eggs were coated with cream only. We also experimentally parasitized prinias with non‐mimetic model eggs with reduced UV reflectance. Yellow‐bellied Prinia and Plain Prinia rejected their own UV‐blocked eggs in 18.2 and 8.3% of the experiments, respectively, and the difference was not significant. However, Yellow‐bellied Prinia rejected 100% of the non‐mimetic eggs, whereas the Plain Prinia rejected only 5%. Hence, UV reflectance alone is a cue in egg discrimination, but the importance of reflectance outside the UV spectrum in these two prinia species is much more responsive to selection as a consequence of brood parasitism.  相似文献   

16.
Interspecific brood parasitism by the common cuckoo (Cuculus canorus) lowers host fitness, and has selected for discrimination and rejection of parasitic eggs in their commonly parasitized hosts. Cognitive demands needed to discriminate and reject cuckoo eggs may have led to augmentation of relative brain size among passerine hosts parasitized by cuckoos. This hypothesis predicts for across species positive relationships of brain size with rejection rate, host suitability and parasitism level. Here we test these predictions while controlling for phylogenetic, ecological and developmental factors known to affect brain size and egg rejection in a comparative study using the cuckoo and their hosts in Europe as a model system. Contrary to expected the rate of rejection of non‐mimetic cuckoo eggs covaried negatively with relative brain size across bird species. Either suitability as cuckoo host, which reflects long‐time duration of exposure to cuckoo parasitism, and level of parasitism, did not relate to brain size. Our results do not support the hypothesis that cuckoo parasitism was a main direct force affecting brain size variation across passerine hosts.  相似文献   

17.
Given the high costs of brood parasitism, avian hosts have adopted different defences to counteract parasites by ejecting the foreign egg or by deserting the parasitized nest. These responses depend mainly on the relative size of the host compared with the parasitic egg. Small hosts must deal with an egg considerably larger than their own, so nest desertion becomes the only possible method of egg rejection in these cases. The use of artificial model eggs made of hard material in egg‐recognition experiments has been criticized because hard eggs underestimate the frequency of egg ejection. However, no available studies have investigated the effect of softer material. Here, we test the potential effect of size of dummy parasitic eggs in relation to egg‐rejection behaviour (egg ejection and nest desertion rates) in Western Bonelli's Warbler Phylloscopus bonelli, a small host, using plasticine non‐mimetic eggs of three different sizes. In addition, we tested the potential effect of material, comparing ejection and desertion responses between real and plasticine eggs. As predicted, small eggs were always ejected, whereas nest desertion occurred more frequently with large eggs, thus suggesting that nest desertion occurs because of the constraints imposed by the large eggs. We found that plasticine may misrepresent the responses to experimental parasitism, at least in small host species, because this material facilitates egg ejection, provoking a decrease in nest desertion rate. Thus, particular caution is needed in the interpretation of the results in egg‐rejection experiments performed using dummy eggs made of soft materials.  相似文献   

18.
MARK BROWN  & MICHAEL J. LAWES 《Ibis》2007,149(2):321-327
Colonial nesters are potentially susceptible to brood parasitism because they present an aggregated source of accessible nests to brood parasites. However, colonial breeding may confer fitness advantages on potential host species that outweigh the costs of parasitism, particularly if colonies are large or dense enough for corporate vigilance to deter parasitism. In addition, some studies have suggested that the spatial habitat structure near host populations is a critical determinant of parasitism rate, with cuckoos targeting those colonies close to cover. We examined the determinants of the likelihood of parasitism by Diderick Cuckoos Chrysococcyx caprius on their main southern African host, the colonially breeding Southern Red Bishop Euplectes orix , from 24 colonies and 1141 nests over two seasons. The likelihood of parasitism by Diderick Cuckoos decreased significantly with increasing colony size and nest density, but not with distance to cover from a colony, providing no support for the spatial habitat structure hypothesis. We suggest that proximate constraints, such as visibility in the semi-closed nest, limit the ability of the host to recognize the Cuckoo egg, giving rise to low rates of rejection of Cuckoo eggs. However, the Cuckoo cannot exploit this apparent weakness when the host breeding population is in large colonies that are protected by corporate vigilance. Consequently, the Diderick Cuckoo – Southern Red Bishop system may represent an evolutionary equilibrium in host and parasite defences.  相似文献   

19.
Many hosts of avian brood parasites such as the common cuckoo (Cuculus canorus) show refined egg discrimination behaviour. Egg recognition in most open‐nesting hosts seems to be based entirely on differences in colour. However, hole‐ and dome‐nesting hosts may rely largely on luminance contrasts. Here, we studied egg rejection behaviour in nightingales (Luscinia megarhynchos), an open‐nesting species that nests in deeply shadowed positions and lays very specific dark olive‐green eggs. Although being theoretically suitable as hosts of the cuckoo, nightingales are very rarely parasitized and no cuckoo egg morph mimicking nightingale eggs is known. Thus, we predicted high rejection rate of foreign eggs, but because of the dim nesting environments, luminance contrasts would be an important cue in egg rejection decisions, similar to cavity‐ or dome‐nesting species. We experimentally parasitized nightingale nests with two groups of model egg types: ‘bright eggs’ and ‘dark eggs’. Within each group, one of the egg types was an effective match while the other type was a poor colour match (whitish vs. pale blue and olive‐green vs. black).We used a discrimination visual model to quantify host‐model egg similarity and compared egg rejection predicted by the model with the observed rejection pattern. Consistent with a scenario of largely luminance‐based egg recognition, blue and white eggs, which had larger achromatic mismatching, were rejected at a higher relative rate than the better achromatic matching black and green eggs. Nightingales showed strong aggression to a cuckoo dummy, suggesting that they were involved in coevolutionary interactions with the cuckoo in the past. However, because of the highly distinct appearance of nightingale eggs relative to the other sympatrically breeding passerines, and the largely luminance‐based egg recognition, this arms race was likely terminated at an early stage.  相似文献   

20.
The southern African subspecies of Jacobin Cuckoo Clamator jacobinus serratus is a brood parasite of a range of host species. While Jacobin Cuckoos do not evict host young, previous research has found that host young rarely survive the nestling period. Here we provide the first records of Jacobin Cuckoo parasitism of a new host species, the Southern Pied Babbler Turdoides bicolor. We investigate rates of brood parasitism and the survival of host young. The Southern Pied Babbler is one of the largest recorded hosts for Jacobin Cuckoos and, unusually, we find that host young tend to survive the nestling period and maintain similar body mass to host young in unparasitized broods. However, host young were less likely to survive to independence than young raised in unparasitized nests, suggesting a post‐fledging reproductive cost to hosts.  相似文献   

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