Clutch variation and egg rejection in three hosts of the pallid cuckoo, Cuculus pallidus

Behaviour ◽  
2010 ◽  
Vol 147 (1) ◽  
pp. 19-36 ◽  
Author(s):  
Naomi Langmore ◽  
Michelle Landstrom ◽  
Robert Heinsohn

AbstractIn theory, hosts of avian brood parasites would benefit by modifying their egg appearance in two ways to help identify mimetic foreign eggs: (i) by laying clutches that are more uniform in appearance and (ii) by laying clutches that differ from those of other females in the population. Support for these theories is inconsistent, and few studies have used objective measures of clutch variation. Here we used reflectance spectrophotometry to quantify within-clutch and between-clutch variation of three host species of an Australian brood parasite, the pallid cuckoo (Cuculus pallidus). We used egg-swapping experiments in which subjects were presented with either a conspecific egg or a heterospecific egg to compare the egg rejection responses of a frequently parasitised host, the white-plumed honeyeater (Lichenostomus penicillatus), with two less frequently parasitised hosts, dusky woodswallows (Artamus cyanopterus) and willie wagtails (Rhipidura leucophrys). As predicted, rejection rate increased as contrast between foreign egg and host clutch increased. Further, the major host showed greater between-clutch variation than the occasional hosts, and also rejected more similar-looking eggs. Contrary to predictions however, within-clutch variation was not lower in the major host, nor was it important in predicting the rejection rate of foreign eggs by the three host species.

2021 ◽  
Vol 9 ◽  
Author(s):  
Yanyi Wang ◽  
Miao Tian ◽  
Jingpeng Liu ◽  
Xingyu Lu ◽  
Anders Pape Møller ◽  
...  

Female common cuckoo (Cuculus canorous) predator-like “bubbling” calls distract host parental attention and reduce the egg rejection rate. Such “bubbling” calls are also frequently used to attract males and deter territorial rivals in intraspecies contact, and these calls are an ancestral character in many cuckoo species. Although hosts have had sufficient time to become familiar with this call and evolve anti-parasitic strategies, why are the hosts fooled by this “bubbling” call? We propose two hypotheses. The first hypothesis proposes that call variation reduces the opportunity for host species to correctly assess cuckoo tricks. In contrast, the second hypothesis proposes that the cost of behavior may prevent the antiparasitic strategy from evolving. In the study, we tested the prerequisites of these hypotheses, by investigating whether cuckoo calls vary during the day and testing whether the predator-like calls suppress bird activities. Based on field recordings from three different areas, we found high overlap in the calls generated during different periods. Oriental great reed warblers (Acrocephalus orientalis), a host species, did not show different responses toward the playback of female common cuckoo calls generated before noon or afternoon. Based on bird count data, we found that predator-like call playback is insufficient for suppressing bird activities. Therefore, none of the prerequisites were supported by our field data. We discuss the potential reasons for our findings and hope to inspire more research examining female cuckoo vocalizations.


2015 ◽  
Vol 11 (7) ◽  
pp. 20150296 ◽  
Author(s):  
Iliana Medina ◽  
Naomi E. Langmore

Many bird species can reject foreign eggs from their nests. This behaviour is thought to have evolved in response to brood parasites, birds that lay their eggs in the nest of other species. However, not all hosts of brood parasites evict parasitic eggs. In this study, we collate data from egg rejection experiments on 198 species, and perform comparative analyses to understand the conditions under which egg rejection evolves. We found evidence, we believe for the first time in a large-scale comparative analysis, that (i) non-current host species have rejection rates as high as current hosts, (ii) egg rejection is more likely to evolve when the parasite is relatively large compared with its host and (iii) egg rejection is more likely to evolve when the parasite chick evicts all the host eggs from the nest, such as in cuckoos. Our results suggest that the interactions between brood parasites and their hosts have driven the evolution of egg rejection and that variation in the costs inflicted by parasites is fundamental to explaining why only some host species evolve egg rejection.


Author(s):  
Mark Erno Hauber

Hosts of obligate avian brood parasites can diminish or eliminate the costs of parasitism by rejecting foreign eggs from the nests. A vast literature demonstrates that visual and/or tactile cues can be used to recognize and reject natural or model eggs from the nests of diverse host species. However, data on olfaction-based potential egg recognition cues are both sparse and equivocal: experimentally-applied, naturally-relevant (heterospecific, including parasitic) scents do not appear to increase egg rejection rates in two host species, whereas unnatural scents (human and tobacco scents) do so in one host species. Here I assessed the predictions that (i) human handling of mimetically-painted model eggs would increase rejection rates, and (ii) applying unnatural or natural scents to mimetically or non-mimetically painted model eggs alters these eggs’ respective rejection rates relative to controls. I studied wild American Robins (Turdus migratorius), a robust rejecter species of the eggs of obligate brood parasitic Brown-headed Cowbirds (Molothrus ater). There was no statistical evidence to support either prediction, whereas poorer color-mimicry was still a predicted cause of greater egg rejection in this data set. Nonetheless, future studies could focus on this and other host species and using these and different methods to apply and maintain the scenting of model eggs to more directly test hosts’ use of potential olfactory cues in the foreign-egg rejection process.


2019 ◽  
Author(s):  
Mikus Abolins-Abols ◽  
Mark E. Hauber

AbstractAvian brood parasites and their hosts are engaged in a coevolutionary battle that can result in the evolution of sophisticated trickery by parasites and novel defence behaviours in hosts. Despite the clear evolutionary and ecological significance of host behaviour, however, we know very little about the mechanisms that regulate host defences, which limits our understanding of both inter- and intraspecific variation in host responses to parasitism. Here we tested whether corticosterone, a hormone known to be upregulated in hosts exposed to parasitism, also mediates one of the most frequent host defences – the rejection of foreign eggs. We experimentally reduced corticosterone levels in free-living brood parasite hosts, American robins Turdus migratorius, using mitotane and found that the likelihood of model egg rejection was significantly lower in the mitotane-treated birds relative to the sham-treated birds. These results demonstrate a causal link between glucocorticoids and egg rejection in hosts of avian brood parasites, but the physiological and sensory-cognitive pathways that regulate this effect remain unknown.


The Auk ◽  
2004 ◽  
Vol 121 (4) ◽  
pp. 1172-1186 ◽  
Author(s):  
Brian D. Peer ◽  
Spencer G. Sealy

Abstract We tested grackles (Quiscalus spp.) to determine whether they retain egg rejection behavior in the absence of the selection pressure of brood parasitism. Neither Bronzed Cowbird (Molothrus aeneus) nor Brown-headed Cowbird (M. ater) parasitism was recorded in 797 Great-tailed Grackle (Q. mexicanus) nests. Cross-fostered Bronzed Cowbird nestlings, but not Brown-headed Cowbird nestlings, fledged from Great-tailed Grackle nests, indicating that Brown-headed Cowbird parasitism does not select for rejection in these grackles. Great-tailed Grackle populations sympatric and allopatric with Bronzed Cowbirds rejected 100% of model cowbird eggs. An allopatric population of Boat-tailed Grackle (Q. major), a sister species of the Great-tailed Grackle, also rejected 100% of model eggs. Egg rejection in the Boat-tailed Grackle has apparently been retained in the absence of parasitism for as long as 800,000 years since it split from the Great-tailed Grackle. The Common Grackle (Q. quiscula), which lays the most variable eggs among the grackles, also has the lowest level of egg rejection—which is consistent with the argument that it may have lost most of its rejection behavior in the absence of parasitism. With extreme intraclutch egg-variation, Common Grackles may be more likely to reject their own oddly colored eggs, which would select against rejection behavior in the absence of parasitism. Those results have significant implications for long-term parasite-host coevolution, because they suggest that egg rejection has been retained in most species of Quiscalus in the absence of parasitism. If typical of the world's avifauna, such retention may force brood parasites to specialize on a few host species and to rarely return to using old hosts, which would readily reject their eggs.


2020 ◽  
Vol 223 (20) ◽  
pp. jeb229609
Author(s):  
Alec B. Luro ◽  
Esteban Fernández-Juricic ◽  
Patrice Baumhardt ◽  
Mark E. Hauber

ABSTRACTColor and spatial vision is critical for recognition and discrimination tasks affecting fitness, including finding food and mates, and recognizing offspring. For example, as a counter defense to avoid the cost of raising the unrelated offspring of obligate interspecific avian brood parasites, many host species routinely view, recognize and remove the foreign egg(s) from their nests. Recent research has shown that host species visually attend to both chromatic and spatial pattern features of eggs; yet how hosts simultaneously integrate these features together when recognizing eggs remains an open question. Here, we tested egg rejection responses of American robins (Turdus migratorius) using a range of 3D-printed model eggs covered with blue and yellow checkered patterns differing in relative square sizes. We predicted that robins would reject a model egg if they could visually resolve the blue and yellow squares as separate features, or accept it if the squares blended together and appeared similar in color to the natural blue–green color of robin eggs as perceived by the avian visual system. As predicted, the probability of robins rejecting a model egg increased with greater sizes of its blue and yellow squares. Our results suggest that chromatic visual acuity and viewing distance have the potential to limit the ability of a bird to recognize a foreign egg in its nest, thus providing a limitation to host egg recognition that obligate interspecific avian brood parasites may exploit.


2009 ◽  
Vol 6 (1) ◽  
pp. 67-69 ◽  
Author(s):  
Nozomu J. Sato ◽  
Kihoko Tokue ◽  
Richard A. Noske ◽  
Osamu K. Mikami ◽  
Keisuke Ueda

As avian brood parasitism usually reduces hosts' reproductive success, hosts often exhibit strong defence mechanisms. While such host defences at the egg stage (especially egg rejection) have been extensively studied, defence mechanisms at the nestling stage have been reported only recently. We found a previously unknown anti-parasitism behaviour in the large-billed Gerygone, which is a host species of the little bronze-cuckoo, a host-evicting brood parasite. The hosts forcibly pulled resisting nestlings out of their nests and dumped them. Although it has been suggested that defence mechanisms at the nestling stage may evolve when host defence at the egg stage is evaded by the parasite, the studied host seems to lack an anti-parasitism strategy at the egg stage. This suggests that the evolutionary pathway may be quite different from those of previously studied cuckoo–host systems. Future research on this unique system may give us new insights into the evolution of avian brood parasitism.


Author(s):  
Sarah Katherine Winnicki ◽  
Bill M. Strausberger ◽  
Nick Antonson ◽  
Dirk E. Burhans ◽  
Justin Lock ◽  
...  

Generalist obligate brood parasites are excellent models for studies of developmental plasticity, as they experience a range of social and environmental variation when raised by one of their many hosts. Parasitic Brown-headed Cowbirds (Molothrus ater (Boddaert, 1783)) exhibit host-specific growth rates, yet cowbird growth rates are not predicted by hosts’ incubation or brooding periods. We tested the novel “growth-tuning” hypothesis which predicts that total asynchrony between cowbirds’ and hosts’ nesting periods results in faster parasitic growth in nests where host young fledge earlier than cowbirds. We tested this prediction using previously-published and newly-added nestling mass data across diverse host species. Total nesting period asynchrony (summed across incubation and brooding stages) predicted cowbird growth; 8-day old cowbirds were heavier in host nests with relatively shorter nesting periods. We further explored the drivers of variation in growth using mass measurements of cowbirds in Song Sparrow (Melospiza melodia (Wilson, 1810)) and Red-winged Blackbird (Agelaius phoeniceus (Linnaeus, 1766)) nests. Our top models included host species (cowbirds grew faster in sparrow nests), numbers of nestmates (slowest when raised alone), and sex (males grew faster). These results confirm that multiple social and environmental factors predict directional patterns of developmental plasticity in avian generalist brood parasites.


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