Brood mate eviction or brood mate acceptance by brood parasitic nestlings? An experimental study with the non-evictor great spotted cuckoo and its magpie host

Some avian brood parasitic nestlings are highly virulent, destroying all host eggs or nestmates, while others accept growing up together with host nestmates. The traditional idea was that all brood parasitic nestlings would benefit from being alone in the host nest. Thus, why do nestlings of some brood parasitic species accept the company of host offspring in the nest? The trade-off hypothesis suggests that brood parasites must balance the costs and benefits of killing host young because of two major potential costs: risk of nest desertion and loss of begging assistance. Here, we test this hypothesis in a non-evictor cuckoo species, the great spotted cuckoo Clamator glandarius and its main host, the magpie Pica pica, by manipulating brood size (1–3 nestlings) and brood composition (only cuckoo, only magpie or mixed) during three consecutive breeding seasons. None of the broods were abandoned by host parents, and cuckoo nestlings alone in the nest tended to grow faster (i.e. wing length). Thus, none of the predictions of the two potential costs on which the trade-off hypothesis is based apply to the great spotted cuckoo–magpie system. Our experimental study could not directly test why chick killing has not evolved in great spotted cuckoos, but the results point in the direction of several possibilities. We suggest that chick killing in great spotted cuckoos may not be adaptive mainly because another, less costly strategy (i.e. outcompeting host nestmates for food), is efficient for successful parasitism of magpie hosts.     

Does the great spotted cuckoo choose magpie hosts according to their parenting ability?

When brood parasites are about to lay an egg, they have to decide which nest to parasitize. The best nest in which to lay will depend on the parenting ability of the host. We have studied selection of magpie (Pica pica) hosts by great spotted cuckoos (Clamator glandarius). Great spotted cuckoos preferentially parasitize large host nests. Nest volume in magpies is a good indicator of territory quality, since there is a negative relationship between magpie nest size and breeding date, and timing of breeding in magpies is known to be positively related to territory quality. Moreover, magpies occupying high-quality territories have high breeding success. Therefore, nest size is positively related to the quality of magpies. Parasitized magpie nests were of greater volume than the nearest neighbouring nest not parasitized by the great spotted cuckoo. In order to test whether the great spotted cuckoos might select high-quality magpie hosts, we manipulated pairs of parasitized and non-parasitized nests with identical laying dates and habitats, introducing into each of the nests the same number of parasitic and non-parasitic eggs. The number of fledglings reared (magpie plus great spotted cuckoo chicks) in naturally parasitized nests was higher than in experimentally parasitized nests. Thus, the probability of survival of the parasite chicks increased if cuckoo eggs were laid in the nests of high-quality hosts originally chosen by the parasite.     

Location of suitable nests by great spotted cuckoos: an empirical and experimental study

Brood parasites depend entirely on their host species to raise their nestlings until independence. Thus, brood-parasite females must discover and select nests that are at a suitable stage for parasitism, and thus, the location of each parasitic egg is crucial in determining the brood-parasite female’s fitness. In relation to host behaviour, one of the main hypotheses proposed to explain how brood-parasite females find and select a suitable nest posits that the most active hosts during nest building should undergo a higher risk of being parasitised (the “host-activity hypothesis”). Here, using the great spotted cuckoo, Clamator glandarius–magpie, Pica pica system, we found that not only cuckoo females parasitise magpie nests regardless of the location and characteristics of nests, but also that the parasite’s observation of host activity near the nest determines a cuckoo female’s decision of laying in a nest. Only one experimental nest (without host activity) was parasitised before the magpie started laying, while 34.14?% of natural active nests were parasitised before the magpie started laying. These observations support the host-activity hypothesis for nest location in great spotted cuckoos.     

Preferential allocation of food by magpies Pica pica to great spotted cuckoo Clamator glandarius chicks

Adult magpies Pica pica provide parasitic great spotted cuckoo Clamator glandarius nestlings with a diet very similar to that fed to their own chicks. In both naturally and experimentally parasitized nests, great spotted cuckoo chicks were fed at a higher rate than magpie chicks in the same nest. This preferential allocation of food by magpie parents to great spotted cuckoo chicks is consistent with the supernormal stimulus hypothesis, because this result implies that cuckoo chicks provide stronger stimuli for parental care than host chicks. Great spotted cuckoo chicks receive most of the food brought to the nest by the foster parents, because they exploit a series of stimuli which jointly (or sometimes individually) operate as a supernormal stimulus. This hypothesis predicts that if any stimulus is masked, the efficiency of the cuckoo in eliciting parental care will decrease. Here, we analyze experimentally the effects of two of these stimuli, preferential feeding of large nestlings and of nestlings with conspicuous palatal papillae. Firstly, when we experimentally introduced one medium-sized (7–9 days) cuckoo chick into an unparasitized magpie nest where the largest magpie chick was 12–15 days old, the cuckoo did not receive significantly more food than the average or the largest magpie chick. Secondly, when unparasitized nests were experimentally parasitized with a cuckoo chick that had its gape painted to mimic that of magpie chicks, the parasitic cuckoo received less food than the average magpie chick.     

Chick recognition and acceptance: a weakness in magpies exploited by the parasitic great spotted cuckoo

Hosts of brood parasites have evolved the ability to discriminate non-mimetic and even mimetic eggs, but not non-mimetic chicks. Here we demonstrate that the great spotted cuckoo Clamator glandarius does not provide its magpie Pica pica host with a super-normal stimulus that helps to avoid recognition, because single cuckoo chicks introduced into otherwise unparasitized magpie nests are not fed at a higher frequency than single magpie chicks introduced to parasitized magpie nests. Another series of experiments demonstrated that magpies have the ability to discriminate cuckoo chicks, mainly when these are introduced at the end of the nestling period, and especially when the cuckoo chick together with a magpie chick is presented to adult magpies outside the nest. This supports the idea that cuckoos exploit the obligatory reaction of magpies to feed all young that have been hatched in their nests and whose signatures they have learnt. Furthermore, the experimental cuckoo chicks in parasitized magpie nests were more likely to be accepted than they were in non-parasitized nests. This supports the hypothesis that magpies may learn to recognise their own nestlings as those present in the nest and may indicate that a comparison between cuckoo and magpie nestlings is the basis of discrimination.     

Micro-evolutionary change in host response to a brood parasite

The relationship between brood parasites and their hosts is usually assumed to result in coevolution, and documentation of changes in extant populations should thus be possible. Here we describe how the ejection rate of eggs of an obligate brood parasite, the great spotted cuckoo Clamator glandarius, by its host, the magpie Pica pica, has recently increased in an area in southern Spain. The ejection rate of great spotted cuckoo eggs in naturally parasitized nests of the magpie increased at a rate of 0.5% year' during the period 1982–1992. This result was verified in a number of field experiments using nonmimetic and mimetic model eggs. The rate of increase in ejection rate was 4.7% year^-1 for mimetic eggs and 2.3% year^-1 for nonmimetic eggs. There were clear differences in parasitism by the great spotted cuckoo between study plots and years, which makes comparisons of rates of parasitism between areas difficult without considering temporal variation. The recent increase in the ejection response of magpies to great spotted cuckoo eggs was not due to magpies using the abundance of cuckoos as a cue to the intensity of parasitism.     

The multidimensionality of behavioural defences against brood parasites: evidence for a behavioural syndrome in magpies?

Studies of antiparasite defences against cuckoo parasites have largely neglected the possibility that behavioural components of host defence may correlate giving rise to a behavioural syndrome. Furthermore, the different contribution of the host’s sex in nest defence has traditionally been disregarded. Here, we studied magpie (Pica pica) mobbing behaviour towards dummies of great spotted cuckoo (Clamator glandarius) and non-harmful hoopoes (Upupa epops) and egg rejection of parasite eggs in a population of colour-banded magpies. We predicted a positive correlation between the intensity of nest defence and egg rejection within each sex and that females respond more intensely than males to the threat of brood parasitism as they undertake incubation. Magpie males, but not females, defended their nests more intensely in those nests in which cuckoo model eggs were rejected. Individual magpies did significantly differ in their baseline level of nest attentiveness; however, there were no individual differences once pair identity was considered. Males and females defended their nests more intensely when it was exposed to the presence of a great spotted cuckoo dummy. Males, but not females, were more prone to appear at their nests, and females, but not males, were more prone to defend more intensely when their nests were challenged by a parasite threat. Our results thus agree with the view that mobbing behaviour and egg rejection in magpies may actually constitute a pseudosyndrome and highlight the necessity to integrate interindividual variation and the sex of the host in studies of the evolution of host defences.     

Breeding success of a brood parasite is associated with social mating status of its host

Reproductive success of brood parasites varies considerably both among and within host species, mainly due to differences in host egg-rejection rates and survival of parasitic chicks. Here, we investigated the breeding success of the cuckoo (Cuculus canorus) in one of its major hosts, the great reed warbler (Acrocephalus arundinaceus), with respect to host social mating status. In this passerine, polygynous males provide less parental care to their young per nest than monogamous males. Consequently, their less-assisted females may fledge lower numbers of nestlings than monogamous females. This may be especially true for secondary females, which often receive limited or no paternal help with young at all. Based on these findings, we expected higher cuckoo reproductive success in nests of socially monogamous than polygynous great reed warbler males. More specifically, we predicted lower fledging success of cuckoo young in nests of secondary than primary or monogamous females. In line with the prediction, we found higher cuckoo fledging success in nests of monogamous than polygynous males, monogamous nests being more than twice as successful as secondary nests. We detected, however, only a tendency to lower cuckoo success in primary compared to monogamous nests and no differences between primary and secondary nests. Moreover, neither parasitism nor host egg-rejection rates differed among the nests of different status. Our results show, for the first time, that the social mating status of a host may influence the overall reproductive success of a brood parasite and thus should be considered in further studies.     

Feeding frequency and parental division of labour in the double-brooded great tit Parus major

Summary We studied the relative contribution of each sex and total effort expended in feeding nestlings in the great tit Parus major in relation to artificially altered brood size. A recent model suggests that feeding frequency should reflect the optimal trade-off between parental and fledgling survival, the former being negatively, the latter positively, influenced by high feeding frequencies. In both sexes weight loss was linearly related to feeding frequency. Since fledgling survival increases with nestling weight, the conditions of this model are fulfilled. However, in contrast to the predictions of the model, the total feeding frequency for both sexes combined did not differ between control and enlarged broods, but was lower for reduced ones. This outcome was not the result of a physiologically related inability of the parents to increase their delivery rate. Instead, we suggest that parents with enlarged broods could not find sufficient amounts of prey large enough to be economically worth transporting to the nest. Differences in brood-provisioning rates between the sexes may arise because costs and benefits of feeding nestlings may differ. Females lost more weight than males during the nesting period, but maintained a relatively higher weight during the incubation period. The relationship between weight loss and feeding frequency was similar for both sexes. Male and female brood-feeding frequency was related to brood size in a similar way. This is discussed in light of the great tit's mating system and the fact that the great tit is facultatively double-brooded.     

The cost of host egg damage caused by a brood parasite: experiments on great spotted cuckoos (Clamator glandarius) and magpies (Pica pica)

Adult great spotted cuckoos, Clamator glandarius, frequently damage one or more eggs of their magpie host, Pica pica, without removing or eating them. The presence of damaged host eggs could signal parasitism thereby increasing the probability that the parasitic egg is ejected. This hypothesis was tested by experimentally introducing a model cuckoo egg with or without damaged host eggs. Magpie responses to experimental parasitism did not differ significantly between treatments implying that damaged host eggs are not used by magpies to assess parasitism. We followed the fate of magpie eggs naturally damaged by the great spotted cuckoo or experimentally damaged by us. Host response was very similar for naturally or experimentally damaged host eggs, but varied significantly according to the type of egg damage, eggs being removed more frequently when pecked than crushed, while cracked eggs were never removed. However, the egg damage that most readily causes egg removal is albumen leakage. Received: 30 November 1998 / Received in revised form: 7 June 1999 / Accepted: 12 June 1999     

Reproductive effort of colonial and solitary breeding tree sparrows Passer montanus L.

A total of 250 nestboxes were arranged in five plots in a suburban area of Budapest, Hungary (19°04E, 47°41N). In each plot, 25 were placed at 50 m intervals to simulate solitary breeding and 25 3–5 m apart to simulate colonial breeding. Length of nest building period, feeding frequency, nestling mortality, nestlings' diet, productivity and parental condition were compared for colonial and solitary breeding tree sparrows Passer montanus. Parents with long nest-building periods, including the majority of first-year females, produced fewer young than parents which built over short periods. Parents fed nestlings morefrequently and nestlings had lower mortality in second than first broods; whether or not a third brood was reared was determined by the costs invested in first and second broods. Females that laid a third clutch had reared fewer young in first and second broods and were heavier than females that reared many young in two broods. Colonial birds had higher feeding frequencies, more similar diets and suffered lower nestling mortality than solitary parents for first broods, but they fed less frequently, diets were less similar, and nestling mortality was higher in second and third broods. It is suggested that colonial breeders benefited from the social stimulation of simultaneous feeding in first broods, but the advantage of synchronicity in feeding declined in second broods and the sparser breeding spacing of solitary parents was more advantageous for feeding in second and third broods. Birds that changed nest spacing between broods had fed nestlings less frequently and had higher nestling mortality before changing than birds which retained their spacing. Parents which changed from colonies to solitary nests fed more frequently with lower nestling mortality in the next brood than parents which retained colonial nests for their second (and third) brood. Solitary parents did not show such a relationship. The rearing of three broods caused higher weight loss in colonial than solitary parents.Correspondence to: L. Sasvári     

Modeling post-fledging survival of Lark Buntings in response to ecological and biological factors

We evaluated the influences of several ecological, biological, and methodological factors on post-fledging survival of a shortgrass prairie bird, the Lark Bunting (Calamospiza melanocorys). We estimated daily post-fledging survival (n = 206, 82 broods) using radiotelemetry and color bands to track fledglings. Daily survival probabilities were best explained by drought intensity, time in season (quadratic trend), ages < or = 3 d post-fledging, and rank given drought intensity. Drought intensity had a strong negative effect on survival. Rank was an important predictor of fledgling survival only during the severe drought of 2002 when the smallest fledglings had lower survival. Recently fledged young (ages < or = 3 d post-fledging) undergoing the transition from nest to surrounding habitat experienced markedly lower survival, demonstrating the vulnerable nature of this time period. Survival was greater in mid and late season than early season, corresponding to our assumptions of food availability. Neither mark type nor sex of attending parent influenced survival. The model-averaged product of the 22-d survival calculated using mean rank and median value of time in season was 0.360 +/- 0.08 in 2001 and 0.276 +/- 0.08 in 2002. Survival estimates that account for age, condition of young, ecological conditions, and other factors are important for parameterization of realistic population models. Biologists using population growth models to elucidate mechanisms of population declines should attempt to estimate species-specific of post-fledging survival rather than use generalized estimates.     

Offspring reproductive value and nest defense in the magpie (Pica pica)

Summary Magpie (Pica pica) brood defense against a human at the nest was studied in a Mediterranean population with low renesting potential. Variations in two defense measures recorded during 106 trials at 41 different nests were positively correlated with brood age. Ineremental effects due to the number of successive visits to nests by us, brood size, and the time in the breeding season were not significant. Partial correlation analyses showed that visit rate was not an important determinant of nest defense, which thus favors an adaptive explanation of nest defense patterns. Two functional hypotheses to account for the increase in defense intensity with brood age were tested: whether (1) increased parental defense serves to compensate the higher predation risk of older nests or (2) increased parental defense reflects the increasing reproductive value of nestlings as they grow older. Daily mortality and incidende of predation (estimated from contribution of whole-brood losses to total mortality) was higher early in the nestling period, hence providing weak evidence for the assumption on which hypothesis (1) is based. The timing of parental defense intensity did not mirror variations in predation risk for the nest but variations in reproductive value of the brood, as can be estimated from daily mortality, thus supporting hypothesis (2). Magpie parents increased defense intensity in response to premature escaping by almost fully-developed nestlings. Since such a response lowers predation risk for the offspring and increases their probability of survival, this finding supports hypothesis (2), but runs contrary to hypothesis (1). Parents also increased defense in response to play-backs of alarm calls uttered by nestlings during escaping episodes. It is argued that parents should continuously monitor the degree of offspring development in order to assess their reproductive value and that, by alarm calling, chicks honestly make their parents aware of the gain in reproductive value that results from enhancement in locomotory abilities that occur at the end of the nestling period.     

Brood parasitism disproportionately increases nest provisioning and helper recruitment in a cooperatively breeding bird

Obligate avian brood parasites lay their eggs in nests of other species (hosts), which raise parasitic young. Parasitic nestlings are likely to influence host’s parental behaviours as they typically beg for food more vigorously than young host for a given hunger level. However, few studies have tested this idea, with conflicting results. These prior studies were largely limited to biparental hosts, but little is known about the effect of brood parasitism on parental behaviours in hosts that breed cooperatively. We followed a multimodel approach to examine the effect of brood parasitism on nest provisioning and helper recruitment in the baywing (Agelaioides badius), a cooperative breeder parasitised by screaming (Molothrus rufoaxillaris) and shiny (Molothrus bonariensis) cowbirds. Multimodel inference results indicated that feeding visits increased with nestling age, cooperative group size and number of cowbird nestlings in the brood. Brood size had little influence on feeding visits, which further suggests that baywings adjusted their provisioning effort in response to cowbird parasitism. In addition, nests parasitised artificially with shiny cowbird eggs or hatchlings recruited more helpers than unmanipulated nests having only host or screaming cowbird young. Our results provide novel evidence that brood parasitism and cooperative breeding interact in determining the levels of nest provisioning.     

Influences of sex,sex composition of brood and hatching order on mass growth in common terns<Emphasis Type="Italic"> Sterna hirundo</Emphasis>

We studied sex-dependent mass growth of chicks of the monomorphic common tern Sterna hirundo which fledged at a colony site in Wilhelmshaven, Germany, between 1997 and 1999. Brood size, brood mates' sex and hatching order (a-, b- and c-chicks) were known for many individuals, which were sexed by molecular techniques. Daily growth rates and age of fledging were independent of sex. However, in all years male chicks reached higher peak mass and fledged up to 5.2% heavier than female chicks. Broods with at least two fledglings showed that besides sex, brood size interacting with sex composition affected chick mass. In mixed broods, brothers had higher peak and pre-fledging mass than sisters they were reared with. Especially in the combination a-daughter and b-son the brothers were heavier. Lowest mass was found in broods with three nest mates of the same sex. A detailed study of 24 three-fledgling broods showed that male c-chicks were heavier than their siblings. The results reveal an advantage for chicks in mixed broods, especially for sons, and more especially if the son was a c-chick. Higher mass and possibly dominance of sons in c-position might be related to higher maternal androgen levels, which are known to increase with each egg laid. The results suggest that even in a monomorphic species, sons might be more expensive to rear, and are discussed with respect to sibling competition, parental effort, survival of sons, as well as to fitness benefits favoring parents producing sons.     

Parental feeding rate in relation to begging behavior in asynchronously hatched broods of the great tit Parus major

Summary Variations in the begging behaviour of the nestlings of altricial birds can provide the parents with information about the nestlings' nutritional needs and thus influence the parental feeding rate. In a series of four experiments, the stimulus situation encountered by great tits on their feeding visits to the brood was manipulated to explore its effect on feeding rate.A higher feeding rate was observed under the following conditions: (1) after a period of food deprivation, as compared with both normal conditions and satiation through artificial feeding; (2) in periods when recorded begging calls were played during feeding visits, as compared with control periods; (3) after temporary removal from the nest of heavier, as compared with lighter, siblings. The lighter nestlings in the brood benefitted more —in terms of gain in weight — from the increase in parental feeding rate following the playing of begging calls than did the heavier nestlings. Differences in weight spread within broods did not affect the amount of food the parents brought.We conclude that parental feeding rate is affected not simply by the begging of the hungriest nestling, but rather by the behaviour of all the nestlings in the brood, which makes possible an adjustment of the feeding rate to the average hunger level of the brood. The effects of hatching asynchrony and sibling competition on parental feeding rate are discussed.     

When to pay the cost of reproduction? A brood size manipulation experiment in great tits (<Emphasis Type="Italic">Parus major</Emphasis>)

Parental investment (PI) theory assumes that optimal parental investment is a function of expected cost/benefit ratio of current versus future reproduction. This study tests the prediction of PI theory that in a species with high adult mortality, paying of reproductive costs can be induced or prevented by manipulation of brood reproductive value (RV). Analysis of recruitment rates in a 10-year study of great tits (Parus major) showed that brood RV was affected by both fledgling number and quality (body mass and tarsus length). A 4-year brood size manipulation experiment (±2 hatchlings) resulted in reduction of fledgling quality in enlarged versus control and reduced broods, while the fledgling number did not differ between manipulation categories due to increase of nestling mortality with brood size manipulation score. Hence, the experiment resulted in reduction of brood RVs in enlarged broods. Females rearing enlarged broods survived better than those with control and reduced broods, while male survival was not affected by the experiment. This indicates that paying the survival costs for reproduction was a part of normal life history for studied female great tits, and that decisions whether to pay this cost were based on the estimation of brood RV. Recruitment rate was lowest (but extremely male-biased) in reduced broods, while control and increased broods did not differ in the number of locally recaptured offspring.     

Generalist cuckoo bees (Hymenoptera: Apoidea: Sphecodes) are species-specialist at the individual level

Intensive and incessant arms races between a parasite and its host are generally expected to lead to parasite specialization. Nevertheless, some parasitic species still successfully attack wide spectra of hosts. One of the solutions to the evolutionary enigma of the long-term existence of generalist parasites is their specialization at an individual level, a phenomenon well known, e.g., in European common cuckoo. Over its range, it parasitizes a number of bird species; however, individual females are mostly specialists possessing adaptations to a particular host species. In this study, we test the possibility of individual specialization in generalist cuckoo bees, the insect counterparts of avian cuckoos. Females of cuckoo bees lay each egg into a single brood cell in the nests of other bee species. The host’s offspring is destroyed by the parasitic female or later by her larvae, which feed on pollen supplies accumulated by the host. Both studied cleptoparasitic bees (Sphecodes ephippius and Sphecodes monilicornis) are widely distributed in Europe, where they have been reported to use broad host spectra. We recorded several host species (including some previously unknown) for both cuckoo bee species, and confirmed that these parasites are indeed generalist even at a small local scale. However, we demonstrate that exactly as in the avian cuckoos, each female in both species of generalist bee parasites tends to attack just one host species.     

Coevolution,communication, and host chick mimicry in parasitic finches: who mimics whom?

Why do brood parasitic Vidua nestlings mimic the intricate gape patterns of their hosts’ young so precisely? The classic explanation is that mimicry is the outcome of a coevolutionary arms race, driven by host rejection of odd-looking offspring. Selection favors parasitic nestlings that converge on the host young’s mouth markings, and simultaneously benefits hosts whose mouth markings diverge from those of the parasite. The outcome is highly elaborate mouth markings in host young that are accurately mimicked by parasite nestlings. Our review of recent work provides mixed support for this traditional view and, instead suggest that complex mouth markings function to stimulate adequate provisioning, rather than to signal species identity. Thus, similarly elaborate gape morphologies in hosts and parasites could have evolved through nestling competition for parental care. According to this view, and in contrast with existing hypotheses, it is host young that mimic parasitic offspring, in order to compete effectively for food.     

Patterns of brood division and an absence of behavioral plasticity in a neotropical passerine

Studies of parental behavior in various habitats provide an opportunity to gain insight into how different environments may mold strategies of parental care. Brood division by parents has been hypothesized to occur facultatively within and among species. Brood division occurs when each parent cares for specific offspring within a brood. We studied brood division in a neotropical passerine, the western slaty antshrike (Thamnophilus atrinucha). Our results present a unique picture of a highly specialized example of avian brood division. Division was a fixed behavioral pattern in the population studied: all broods divided by fledging and remained divided during the entire post-fledging period. Brood division before fledging, a previously unreported phenomenon, occurred in 40% of nests observed. Parents that preferentially fed a certain offspring (defined as their focal offspring) in the nest fed the same individual after fledging. Each parent fed only its focal offspring in broods of one and two. The male parent cared for the heavier offspring and the first offspring to leave the nest. Siblings were segregated spatially during the time of highest predation risk. These observations suggest that a consistently high risk of predation on offspring has favored initial spatial segregation and inflexibility of brood division behavior in this species. Factors other than predation risk alone may explain the observed patterns of long-term, perfect brood division. Because high predation is common and relatively predictable in the tropics, selection for fixed brood division may be stronger in tropical birds than in the temperate zone.