How to hatch from an egg of great structural strength. A study of the Common Cuckoo

Brood parasitism represents a unique mode of avian reproduction that requires a number of adaptations. For example, to reduce chances of puncture ejection of their eggs by small hosts, brood parasites may have been selected for laying eggs of unusually great structural strength. However, great structural strength of eggshells should hinder hatching. The goals of our study were to establish if chicks of the Common Cuckoo Cuculus canorus have more difficulty with hatching out of their strong eggs than chicks of species with eggs of similar size, and whether they possess any mechanisms facilitating hatching. To achieve these goals, we compared hatching pattern and selected body characteristics of chicks of the Common Cuckoo with those of another altricial species with eggs of a similar size, the Great Reed Warbler Acrocephalus arundinaceus . Although the rate of pecking was similar in the two species, the Common Cuckoo chicks started pecking earlier in relation to their emergence and consequently required more time and a greater cumulative number of pecks for breaking open their eggs than did young Great Reed Warblers. The two species also differed with respect to the pattern of opening their shells; in contrast to the warbler chicks, which enlarged the original pip circularly, the cuckoo chicks opened the egg by systematically creating a long narrow slit until they emerged. Finally, our study of hatched young revealed several differences; the Cuckoo hatchlings were significantly heavier, had a longer forearm, and their egg tooth was located significantly farther from the tip of the beak. The edge used for cutting through the shell was also significantly longer than that of hatchling Great Reed Warblers. To conclude, our data suggest that hatching is more difficult for a Cuckoo than for a Great Reed Warbler and that Cuckoos possess several mechanisms to overcome the problems of hatching from a structurally strong egg.     

Common Cuckoo Cuculus canorus and host behaviour at Reed Warbler Acrocephalus scirpaceus nests

This study is based on continuous video recordings made at 53 Reed Warbler Acrocephalus scirpaceus nests each day during the laying period. Egg-laying by the Common Cuckoo Cuculus canorus was recorded in 14 (26.4%) of these nests. By analysing the activity of the host birds around and at the nest, we found that this is probably not the only cue used by the Common Cuckoo when locating suitable nests to parasitize. Furthermore, in most cases there was no significant difference between the length of time the host birds spent at the nest in the morning and afternoon, thus providing little support for the hypothesis that the Common Cuckoo lays in the afternoon because it is less likely to be seen by the nest owners then. Parasitized Reed Warblers rejected the Common Cuckoo egg more frequently when they observed the parasite at their nests. However, contrary to what should be expected, most Common Cuckoos laid their eggs in the presence of the host(s), and in general their egg-laying behaviour (for example duration of stay at the nest) was less secretive than described earlier. When partially depredating host clutches, Cuckoos showed the same behavioural pattern at parasitized and unparasitized nests, indicating that the latter may act as a potential reserve for egg-laying.     

Parasitierung und Brutverluste durch den Kuckuck (Cuculus canorus) bei Teich- und Sumpfrohrs?nger (Acrocephalus scirpaceus,A. palustris) in Mittel- und Westeuropa

Zusammenfassung Nach 52 brutbiologischen Untersuchungen und Angaben der Parasitierung durch den KuckuckCuculus canorus bei Teich- und SumpfrohrsängernAcrocephalus scirpaceus,A. palustris wird für Mittel- und Westeuropa eine durchschnittliche Parasitierung von 8,3±7,8 % bei Teich- und von 6,3±6,6 % bei Sumpfrohrsängern berechnet (Tab. 1). Wegen der hohen Streuung beträgt der Median beim Teichrohrsänger 9 % und beim Sumpfrohrsänger nur 1,2 %. Selbst unter der Annahme einer gewissen Unausgewohgenheit des Datenmateriales übertreffen diese Werte bei weitem die aller anderen häufigen Kuckuckswirte in Mittel- und Westeuropa. Die Parasitierung des Teichrohrsängers ist fast flächendeckend, beim Sumpfrohrsänger dagegen mehr lückig über die Region verteilt (Abb. 1). Die Parasitierungsfrequenz scheint im Osten und Süden geringer als im Nordwesten. Ihre hohe Brutbestandsdichte macht die beiden Rohrsänger zu idealen Kuckuckswirten. Es gibt Hinweise, daß die Parasitierung bei beiden Arten zunimmt (Abb. 2). Darüberhinaus werden auch zahlreiche Gelege von den Kuckucksweibchen geraubt. Diese Verluste können viermal so hoch sein wie die durch Parasitierung (s. auch Abb. 3). Beide Arten haben zahlreiche Abwehrmechanismen gegenüber dem Kuckuck, wobei die Eiablehnung durch den Sumpfrohrsänger viel heftiger und effektiver ist als beim Teichrohrsänger. Möglicherweise steht der Sumpfrohrsänger unter einem höheren selektiven Druck für erfolgreiches Brüten.

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Parasitism and egg losses due to the Cuckoo (Cuculus canorus) in Reed and Marsh Warblers (Acrocephalus scirpaceus,A. palustris) in central and western Europe

Summary Both Reed and Marsh Warblers are common Cuckoo hosts. In this paper the frequencies of Cuckoo parasitism in 52 studies dealing with breeding success as well as parasitism in both warblers over a wide range of central and western Europe are analysed. Average parasitism rates are 8.3±7.9 % in Reed and 6.3±6.6 % in Marsh Warblers (tab. 1). Taking the high variation coefficient into consideration the median of Reed Warbler parasitism is 9 % and of Marsh Warbler parasitism only 1.2 %. Due to the uneven distribution of the studies over the region analysed and due to the preference by the researchers for smaller study plots vs large habitats there might be some bias towards higher parasitism figures. Nevertheless, both warblers range on top of the list of Cuckoo hosts and have much higher parasitism rates than other common hosts. Parasitism of the Reed Warbler does occur over the whole region, whereas in the Marsh Warbler it is more unevenly and patchily distributed. Parasitism seems to be higher in the northwestern than in the eastern and southern parts of central and western Europe. Both warblers are ideal hosts due to their high population densities in good habitats. There are indications for an increase of parasitism in both species during the last 30–50 years. Besides parasitism, many clutches of both warblers are predated upon by female Cuckoos. The number of predated nests can be four times as high as the number parasitized (see also Fig. 3). Both species exhibit a broad array of counter-reactions against the Cuckoo. The egg rejection by Marsh Warblers is much stronger and much more effective than in the Reed Warbler. Probably Marsh Warblers are under a higher selection pressure for successful breeding than Reed Warblers or have a different strategy to avoid losses.

     

European Cuckoo Cuculus canorus parasitism and host's rejection behaviour in a heavily parasitized Great Reed Warbler Acrocephalus arundinaceus population

An unusually high frequency (64%) of European Cuckoo Cuculus canorus parasitism was found in Great Reed Warbler Acrocephalus arundinaceus clutches in central Hungary. Sixty-four per cent of the parasitized clutches contained one Cuckoo egg, 23% contained two, 10% had three and 3% had four. This means that 58% of the Cuckoo eggs were found in multiply parasitized clutches. In multiple parasitism the laying second Cuckoo removed an egg from the clutch randomly, so preferred neither the host eggs, nor the concurrent Cuckoo egg. Host response towards the parasitic eggs showed 66% acceptance, 12% ejection, 20% desertion and 2% egg burial. We found great variation in both the host and the parasitic egg colour and pattern. This reduces the chance that the parasitic egg's appearance matched that of the hosts' but, in spite of this, almost perfect mimesis was found in 28% of the Cuckoo eggs. Poorly mimetic Cuckoo eggs were more frequently rejected by Great Reed Warblers than parasite eggs that were very similar to the host eggs. This high level of mimicry sometimes makes it difficult for the observer to identify the parasitic egg, especially when it is similar in size to the host eggs. It is also difficult for the host, as shown by the relatively high recognition error and ejection cost.     

Common Cuckoos Cuculus canorus change their nest‐searching strategy according to the number of available host nests

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.     

Brood-parasitism by the Shining Cuckoo Chrysococcyx lucidus at Kaikoura, New Zealand

For three seasons starting in 1976 I studied the breeding of Shining Cuckoos Chrysococcyx lucidus in forest near Kaikoura, New Zealand. There is no evidence that the cuckoo parasitizes any host on mainland New Zealand other than the Grey Warbler Gerygone igata. A nestling cuckoo returned to within 1 km of its natal site in a subsequent breeding season, presumably after migrating beyond New Zealand. Empirical and theoretical estimates of the area occupied by Shining Cuckoos while breeding are given. Cuckoos near Kaikoura laid during ten weeks, the modal week of laying following seven weeks after the presumed peak of arrival of birds in New Zealand. First clutches of the host escaped parasitism because they were laid before most cuckoos arrived. Parasitized clutches received one cuckoo egg which replaced a host's egg. It was laid before, just after or long after the host began incubating, and mimicry was lacking. Cuckoo eggs, which were about 8% of the adult cuckoo's weight, hatched in 14–17 days. The frequency of parasitism near Kaikoura was 55% of late clutches (n = 40).
At 3–7 days old, nestling Shining Cuckoos evicted from the nest all other contents. The nestling period was at least 19 days. Growth in weight followed a logistic curve and the equation is given. Just over half the cuckoo eggs produced fledglings. The effect of brood-parasitism on the Grey Warbler's productivity was small. Only 17% of late warbler eggs, and late eggs only, were prevented by parasitism from yielding fledglings. Late laying by some Shining Cuckoos (relative to the host's incubational cycle), and late eviction, often led to brief inter-specific competition among nestlings for food. The brief coexistence of young Warblers and Cuckoos in the nest may explain the apparent mimicry by newly-hatched Shining Cuckoos of the host's young.     

Breeding ground correlates of the distribution and decline of the Common Cuckoo Cuculus canorus at two spatial scales

Many migratory bird species are undergoing population declines as a result of potentially multiple, interacting mechanisms. Understanding the environmental associations of spatial variation in population change can help tease out the likely mechanisms involved. Common Cuckoo Cuculus canorus populations have declined by 69% in England but increased by 33% in Scotland. The declines have mainly occurred in lowland agricultural landscapes, but their mechanisms are unknown. At both the local scale within the county of Devon (SE England) and at the national (UK) scale, we analysed the breeding season distribution of Cuckoos in relation to habitat variation, the abundance of host species and the abundance of moth species whose caterpillars are a key food of adult Cuckoos. At the local scale, we found that Cuckoos were more likely to be detected in areas with more semi‐natural habitat, more Meadow Pipits Anthus pratensis (but fewer Dunnocks Prunella modularis) and where, later in the summer, higher numbers of moths were captured whose larvae are Cuckoo prey. Nationally, Cuckoos have become more associated with upland heath characterized by the presence of Meadow Pipit hosts, and with wetland habitats occupied by Eurasian Reed Warbler Acrocephalus scirpaceus hosts. The core distribution of Cuckoos has shifted from south to north within the UK. By the end of 2009, the abundance of macro‐moth species identified as prey had also declined four times faster than that of species not known to be taken by Cuckoos. The abundance of these moths has shown the sharpest declines in grassland, arable and woodland habitats and has increased in semi‐natural habitats (heaths and rough grassland). Our study suggests that Cuckoos are likely to remain a very scarce bird in lowland agricultural landscapes without large‐scale changes in agricultural practices.     

The role of reed management and habitat quality on brood parasitism and chick survival of the brood parasitic Common Cuckoo

Despite efforts on ecosystem restoration and management, biodiversity loss remains one of the major environmental concerns of our time. Beyond the focus on threatened species, animals that indicate regional biodiversity hotspots and population trends, such as brood parasites, should also be targeted by conservation actions. We studied how reed habitat quality and management influence brood parasitism rate and offspring survival in Common Cuckoos Cuculus canorus parasitizing nests of Great Reed Warblers Acrocephalus arundinaceus in six reed habitats in an intensive agricultural landscape. Data collected from 45 sites over 13 years showed that the brood parasitism rate was highest on large canals and was positively influenced by the availability of potential perches (Cuckoo vantage points) and the height where host nests were built. Cuckoo chick survival decreased with water depth and was not affected by other factors. Our results suggest that the habitat-dependent detectability of host nests was central in brood parasitism rate and that water level was central in Cuckoo chick survival. Our study shows that a maintenance of intermediate water levels is the most optimal for maintaining Cuckoo populations in intensive agricultural landscapes. Because brood parasites are excellent bioindicators as their presence predicts regional hotspots of taxonomic and functional diversity as well as population trends in bird communities, knowledge on their habitat requirements is relevant in management targeting diverse bird communities.     

CuckooCuclus canorus parasitism onAcrocephalus Warblers in Southern Moravia in The Czech Republic

Summary The Reed Warbler,Acrocephalus scirpaceus, in the Lednice area, Southern Moravia in the Czech Republic, was parasitized by the Cuckoo,Cuculus canorus, at a rate of at least 18.0 %. The Cuckoo eggs showed poor mimesis with the Reed Warbler eggs, but showed a greater resemblance to the eggs of other species breeding in the area, including the Great Reed Warbler,A. arundinaceus. This latter species was also parasitized, but we did not find enough nests to obtain a reliable estimate for the rate of parasitism. The parasitized Reed Warblers rejected the Cuckoo eggs at a high rate (42.1 %) and therefore both the hatching success and the breeding success of the Cuckoo was considerably lower than shown by comparable results from Britain. On the background of these results (poor mimesis of the Cuckoo eggs and a high rejection rate by the hosts) the question of the degree of specialization versus generalism in the Cuckoo's host preference is discussed.

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Zusammenfassung Teichrohrsänger im Gebiet von Lednice (Südmähren, Tschechei) waren mindestens zu 18 % vom Kuckuck parasitiert. Die Kuckuckseier glichen jenen der Teichrohrsänger nur wenig, waren jedoch den Eiern anderer im Gebiet brütender Arten einschließlich des Drosselrohrsängers ähnlicher. Drosselrohrsänger waren auch parasitiert; wir fanden jedoch nicht genug Nester, um eine Parasitierungsrate ermitteln zu können. 42,1 % der Kuckuckseier wurden vom Teichrohrsänger nicht angenommen; daher waren Schlüpf- und Ausfliegerate des Kuckucks merklich geringer als in vergleichbaren Ergebnissen aus Großbritannien. Vor dem Hintergrund unserer Ergebnisse — geringe Angleichung der Kuckuckseier und hohe Ablehnungsrate durch die Wirtsart — wird die Frage von Spezialisierung und Generalismus in der Wirtswahl des Kuckucks diskutiert.

     

Nest defence,enemy recognition and nest inspection behaviour of experimentally parasitized Reed Warblers Acrocephalus scirpaceus

Capsule Reed Warblers in a regularly parasitized population do not recognize Cuckoo Cuculus canorus as a special enemy and do not change their behaviour at nest immediately after being parasitized.

Aims To assess if an intruder near the nest influences the behaviour of the Cuckoo host.

Methods Host responses to Cuckoo, control Pigeon dummies and human intruder were observed. Host behaviour at 71 nests was video-recorded for 30 minutes at four experimental groups of nests: Cuckoo dummy, Cuckoo dummy + Cuckoo egg, Pigeon dummy, human intruder.

Results Reed Warblers did not respond differently to the Cuckoo and the control species. The experimental procedure had no significant effect on the behaviour of hosts during the study period. We were unable to find any differences in the time spent at the nest, clutch inspection behaviour and nest defence behaviour between morning and afternoon experimental groups. Our results do not support the hypothesis that afternoon laying by the Cuckoo is maintained by a selection pressure from the host. We observed no ejection or egg-pecking during the 30-min period after the experimental parasitism.

Conclusions Low aggression and non-specificity of host responses in our study area are in line with the fact that the Reed Warbler is an intermediate rejecter of Cuckoo eggs as expected from the spatial habitat structure hypothesis.     

Provisioning of nestling Cuckoos Cuculus canorus by Reed Warbler Acrocephalus scirpaceus hosts

Reed Warblers Acrocephalus scirpaceus fostering a single nestling Cuckoo Cuculus canorus bring food to it at roughly the same rate as they do to an average-sized brood (three or four) of their own young. The food brought, mostly flies and beetles, is also similar. We conclude that the Cuckoo does not provide a supernormal stimulus. We show that Reed Warblers, given experimentally-enlarged broods of seven or eight, can substantially increase their feeding rate. This raises the question of why the young Cuckoo does not exploit this 'spare' feeding capacity of the Reed Warbler hosts. We offer three explanations', (i) that the increased begging necessary would attract predators, (ii) that the young Cuckoo is unable to grow faster, and (iii) that it would not be to the advantage of a young Cuckoo, dependent on its foster parents for about 5 weeks (cf. 3 weeks for Reed Warbler young), to provoke a feeding rate that the warblers could not sustain.     

Vocal mimicry by the Black-browed Reed Warbler Acrocephalus bistrigiceps: objective identification of mimetic sounds

Vocal mimicry by the Black-browed Reed Warbler Acrocephalus bistrigiceps was investigated. To identify mimicry objectively, we measured similarities between the sounds of models and those of Warblers by means of Principal Component Analysis (PCA) using a set of acoustic parameters. Of the sounds suspected of being mimicry according to visual inspection of sonagrams, only 57% were identifiable as mimicry according to PCA. Previous studies have not included quantitative criteria for assessing vocal mimicry, and our results suggest that judgements might not be reliable in the absence of objective criteria. Male Warblers incorporated the mimetic sounds into their songs, and each male mimicked 2–5 species. We found no evidence that females preferred males with large mimetic repertoires. This suggests that vocal mimicry has not evolved in response to selection by females in this species, although our analysis did not reveal entire mimetic repertoires in the Warbler songs.     

Presence of Cuckoo reliably indicates high bird diversity: A case study in a farmland area

Here we studied the occurrence of Cuckoo Cuculus canorus and top predators as indicators of biodiversity in agro ecosystems of Western Poland, to identify local hotspots. Bird species richness and land-use diversity were used as measures of biodiversity. The relationship between the presence of Cuckoos and four avian top predators with biodiversity measures were examined using Generalized Linear Mixed Models.Cuckoos were mainly distributed on sites with greater species richness, but were absent from the low species richness sites, while the top predators were distributed uniformly. The performance of the best models using the presence of Cuckoo was 27% higher than the best models using top predators. Our results highlight the predictive capacity of Cuckoos as an indicator of bird species richness than top predators and the usefulness of this species in biodiversity studies. The cookoo is charismatic, widespread across the main types of landscapes, and is easy to detect from its song. Importantly, our findings propose that cookoo can be used as effective and cheap tool to monitor the high bird diversity in different European countries.     

A protective function for aggressive mimicry?

Mimicry often involves a protective element, whereby the risk of predation on mimics is reduced owing to their resemblance to unpalatable models. However, protection from predation has so far seemed unimportant in aggressive mimicry, where mimics are usually predators rather than prey. Here, we demonstrate that bluestriped fangblennies (Plagiotremus rhinorhynchos), which are aggressive mimics of juvenile bluestreak cleaner wrasse (Labroides dimidiatus), derive significant protection benefits from their resemblance to cleaner fish. Field observations revealed that mimetic fangblennies were chased by potential victims less often than individuals of a closely related, ecologically and behaviourally similar but non-mimetic species (Plagiotremus tapeinosoma). After attacks, proximity to models protected mimics from retaliation by victims, but the effect of colour similarity was less clear. Both colour resemblance and physical proximity to models thus appear to protect cleaner-fish mimics from aggression by potential and actual victims of their attacks. Our results suggest that the mimicry types observed in nature, which are usually distinguished on the basis of the benefits accrued to mimics, may in fact overlap greatly in the benefits provided.     

When should Common Cuckoos Cuculus canorus lay their eggs in host nests?

Capsule Brood parasitic Common Cuckoo Cuculus canorus chicks hatch earlier than the nestlings of their Great Reed Warbler Acrocephalus arundinaceus hosts, but hatching priority is less consistent when Cuckoo eggs are laid after the onset of host incubation.

Aim To reveal by field observations what the optimal stage is for Cuckoos to lay their eggs in relation to the host laying cycle to ensure prior hatching of the parasitic chicks.

Methods We monitored the hatching of Cuckoo chicks in relation to the hosts’ laying stage at which the Cuckoo eggs appeared and also monitored host incubation behaviour.

Results Great Reed Warblers incubated more on day 5 after the host's onset of laying relative to day 3. All Cuckoo eggs hatched earlier than hosts when they were laid prior to the onset of host incubation (day 4). Cuckoo eggs also maintained hatching priority in about 2/3 of the nests when laid on days 5–6.

Conclusions Most Cuckoo eggs are laid prior to the onset of host incubation and this, together with other adaptive mechanisms, ensures the prior hatching of Cuckoo eggs. Cuckoo eggs laid after the onset of incubation lose the advantage of prior hatching in approximately 30% of nests.     

大杜鹃和东方大苇莺卵的人工孵卵期和孵化率比较

大杜鹃(Cuculus canorus)是一种专性巢寄生鸟类,进化出了一系列适应对策,如雏鸟普遍出壳较早等,以更好适应寄生生活。本研究使用恒温自动孵化箱对25枚大杜鹃卵和20枚其宿主东方大苇莺(Acrocephalus orientalis)卵进行人工孵化,并对孵卵期的卵重进行连续测量。结果表明,在人工孵化条件下,大杜鹃卵的孵化率(76%)极显著高于东方大苇莺(40%)(χ~2=25.144,df=1,P0.01)。尽管大杜鹃的卵鲜重(t=7.447,df=43,P0.01)和卵体积(t=8.817,df=43,P0.01)均极显著大于东方大苇莺,但两种鸟卵的孵卵期不存在显著性差异(t=1.006,df=16,P0.05)。     

Breeding phenology,reproductive traits and apparent survival of sympatric Marsh Warbler Acrocephalus palustris and Blyth’s Reed Warbler Acrocephalus dumetorum

Capsule: Sympatric Marsh Warblers Acrocephalus palustris and Blyth’s Reed Warblers Acrocephalus dumetorum differ significantly in their life history traits.

Aims: To provide a direct comparison of demographic parameters among two sympatric populations of the closely related Marsh Warbler and Blyth’s Reed Warbler.

Methods: We examined breeding phenology and reproductive traits at a 25?ha study plot. We use program MARK to estimate daily nest survival and adult apparent survival rates.

Results: On average, Marsh Warblers laid the first eggs 3 days later than Blyth’s Reed Warblers. Mean clutch size in the Marsh Warbler was significantly lower than in the Blyth’s Reed Warbler. There are no significant differences between the two species for nest daily survival, duration of incubation and nestling periods. Apparent survival of adults was slightly higher in Marsh Warblers than in Blyth’s Reed Warblers.

Conclusion: Our findings suggest that two ecologically similar sympatric species differ significantly in terms of life history traits. We assume that observed differences could be the result of adaptations to environmental factors in the central parts of the species’ ranges or due to differences in mortality on migratory pathways or wintering grounds.     

Who Resembles Whom? Mimetic and Coincidental Look-Alikes among Tropical Reef Fishes

Studies of mimicry among tropical reef-fishes usually give little or no consideration to alternative explanations for behavioral associations between unrelated, look-alike species that benefit the supposed mimic. I propose and assess such an alternative explanation. With mimicry the mimic resembles its model, evolved to do so in response to selection by the mimicry target, and gains evolved benefits from that resemblance. In the alternative, the social-trap hypothesis, a coincidental resemblance of the model to the “mimic” inadvertently attracts the latter to it, and reinforcement of this social trapping by learned benefits leads to the “mimic” regularly associating with the model. I examine three well known cases of supposed aggressive mimicry among reef-fishes in relation to nine predictions from these hypotheses, and assess which hypothesis offers a better explanation for each. One case, involving precise and complex morphological and behavioral resemblance, is strongly consistent with mimicry, one is inconclusive, and one is more consistent with a social-trap based on coincidental, imprecise resemblance. Few cases of supposed interspecific mimicry among tropical reef fishes have been examined in depth, and many such associations may involve social traps arising from generalized, coincidental resemblance. Mimicry may be much less common among these fishes than is generally thought.     

Apomorphine as an emetic for insectivorous songbirds: effectiveness and post‐release effects on survival and mass change

Emetics can be used to obtain food samples from birds, but they can harm birds during or after treatment. Studies to date suggest that apomorphine is a safe emetic for songbirds, but information is needed about possible post‐release deleterious effects. From March to July 2012, we collected food samples from insectivorous songbirds using apomorphine. We treated 67 Moustached Warblers (Acrocephalus melanopogon), 56 Reed Warblers (Acrocephalus scirpaceus), 15 Great Reed Warblers (Acrocephalus arundinaceus), and 12 Savi's Warblers (Locustella luscinoides). Effectiveness in inducing regurgitation was high (76.7%) and varied among species, being significantly more effective with Reed Warblers (91.1%). No birds died during treatment. To check for possible post‐release negative effects, we considered 53 treated Moustached Warblers and 37 treated Reed Warblers and selected an equal number of untreated individuals (simply captured, banded, and measured). We found no support for differences in survival or recapture probabilities between treated and untreated birds of either species within 21 d after administering apomorphine. We calculated body mass changes of all Moustached Warblers subsequently recaptured (within 21 d) and found no difference between treated (N = 8) and untreated (N = 22) birds, suggesting normal foraging activity after release. Our results suggest that apomorphine is a safe emetic, with no negative effect on survival at least in the short term. The effectiveness of apomorphine with insectivorous songbirds in our study contrasts with the results of some previous studies and confirms the differences in effectiveness among different taxa of songbirds. As with differences in effectiveness among species in our study, this variability in sensitivity to the emetic could be caused by morphological and physiological differences among different taxa.