Intensity of mouth coloration in Blackcap Sylvia atricapilla nestlings affects food distribution among siblings but not provisioning of the whole brood

Among various begging stimuli, mouth coloration has received increasing attention in recent years, and previous research has demonstrated that mouths of nestling Canaries Serinus canaria get redder with the extent of food deprivation and that parents preferentially feed nestlings of redder gapes. This study assesses whether the intensity of red mouth colour in nestling Blackcaps Sylvia atricapilla is a signal in parent–offspring communication. This is one of the few species with a naturally red gape in which the function of mouth redness has been tested. Three predictions were experimentally tested: (1) reddening the gape of a single nestling within a brood increases its provisioning in relation to other siblings; (2) reddening the gapes of all nestlings within a brood increases parental feeding rate; and (3) food deprivation increases nestling mouth redness. The effect of nestling quality on mouth redness was also assessed. The intensity of gape coloration affected food distribution, but in a way opposite to that expected: an increase in mouth redness of the nestling caused reduced feeding by parents. However, reddening the gapes of all nestlings had no effect on provisioning of the whole brood, suggesting that Blackcap parents use different cues for provisioning particular nestlings and the whole brood. Intensity of mouth redness in Blackcap nestlings was not affected either by food deprivation or by nestling quality in terms of mass and rank in the nest.     

Nestling detectability affects parental feeding preferences in a cavity-nesting bird

In many avian species, nestlings have evolved striking plumage, behaviours and mouth colours to obtain a greater share of parental investment. Studies revealing parental feeding preferences for nestlings with red gapes have proposed that red mouth colour in songbirds can act as a signal of nestling need or condition. Alternative hypotheses suggest that bright nestling mouths in cavity-nesting birds evolved to increase nestling detectability by the parents. We tested whether nestling mouth colour affects parental feeding preferences in great tits, Parus major L. In broods of six young, we experimentally painted mouth gapes and flanges either red or yellow and tested the effect of mouth colour on nestlings' mass gain under two lighting conditions. In nests with high luminosity, there was no significant effect of mouth colour on mass gain. In nests with low luminosity, nestlings with red gapes and flanges gained less mass than nestlings with red gapes and yellow flanges or both yellow gapes and flanges. Our results suggest that, in nests with low luminosity, red mouths decreased nestling detectability to the feeding parents and support the hypothesis that poor luminosity in nesting cavities can select for pale mouths. Overall, our results do not support the hypothesis that red mouth colour signals nestling need or condition to parent great tits.     

Detectability matters: conspicuous nestling mouth colours make prey transfer easier for parents in a cavity nesting bird

An often underappreciated function of signals is to notify receivers of the presence and position of senders. The colours that ornament the mouthparts of nestling birds, for example, have been hypothesized to evolve via selective pressure generated by parents'' inability to efficiently detect and feed nestlings without such visually conspicuous targets. This proposed mechanism has primarily been evaluated with comparative studies and experimental tests for parental allocation bias, leaving untested the central assumption of this detectability hypothesis, that provisioning offspring is a visually challenging task for avian parents and conspicuous mouths help. To test this assumption, I manipulated the mouths of nestling house sparrows to appear minimally and maximally conspicuous, and quantified prey transfer difficulty as the total duration of a feeding event and the number of transfer attempts required. Prey transfer to inconspicuous nestlings was, as predicted, more difficult. While this suggests that detectability constraints could shape nestling mouth colour evolution, even minimally conspicuous nestlings were not prohibitively difficult for parents to feed, indicating that a more nuanced explanation for interspecific diversity in this trait is needed.     

Better red than dead: carotenoid-based mouth coloration reveals infection in barn swallow nestlings

Nestling birds solicit food from their parents by displaying their open brightly coloured gapes. Carotenoids affect gape colour, but also play a central role in immunostimulation. Therefore, we hypothesize that, by differentially allocating resources to nestlings with more brightly coloured gapes, parents favour healthy offspring which are able to allocate carotenoids to gape coloration without compromising their immune defence. We demonstrated that, in the barn swallow Hirundo rustica, (i) parents differentially allocate food to nestlings with an experimentally brighter red gape, (ii) nestlings challenged with a novel antigen (sheep red blood cells, SRBCs) have less bright gape colour than their control siblings, (iii) nestlings challenged with SRBCs but also provided with the principal circulating carotenoid (lutein) have more brightly coloured red gapes than their challenged but unsupplemented siblings and (iv) the gape colour of nestlings challenged with SRBCs and provisioned with lutein exceeds that of siblings that were unchallenged. This suggests that parents may favour nestlings with superior health by preferentially feeding offspring with the brightest gapes.     

Decoding colouration of begging traits by the experimental addition of the appetite enhancer cyproheptadine hydrochloride in magpie Pica pica nestlings

The colouration of some traits in nestlings of altricial birds may influence parental food allocation as it may reflect physical condition or hunger. There is increasing evidence of the relationship between colouration of begging traits and nestling performance. However, evidence of the influence of hunger level on nestling colouration is scarce, mainly because of difficulty of distinguishing between the effects of physical condition and hunger levels. Here, we used the appetite stimulant cyproheptadine hydrochloride to increase the sensation of hunger of magpie Pica pica nestlings for eight days and assessed the effect on the colouration of rictal flanges, mouth and body skin. We found that nestlings administered with cyproheptadine had flanges more conspicuous (chromatic visual contrast), more UV coloured and less yellow coloured than their control nestmates. Conversely, mouths of experimental nestlings were more yellow coloured and less UV coloured than controls. Our pharmacological experiment affected the strength of the relationship between body mass and some colour components of body skin (chromatic and achromatic visual contrasts, UV–chroma and yellow–chroma) and of rictal flanges (chromatic visual contrasts, UV–chroma and yellow–chroma), but not for mouth colouration. These results taken together suggest that the effect of the cyproheptadine on nestling colourations is probably mediated by an increase in hunger levels of nestlings for rictal flanges and body skin colourations, and by an increase in physical condition in the case of mouth coloration.     

Mouth coloration of nestlings covaries with offspring quality and influences parental feeding behavior

Altricial nestlings compete with their nest mates for resourcesdelivered by parents. Parents may allocate food to nestlingsbased on reproductive value of offspring. To test the hypothesisthat mouth coloration acts as a signal of nestling conditionin the barn swallow Hirundo rustica, we investigated whethergape coloration is correlated with offspring quality and age.We also examined the role of ultraviolet (UV) flange colorationin parental allocation in a manipulative experiment. Mouth colorationchanged with age, probably due to accumulation of dietary carotenoidsin the tissue and an increase in the number of collagen layers.Highly UV and redder palates and brighter flanges were associatedwith longer tarsi and greater body mass at day 6 and with feathergrowth at day 12 posthatching. Although we did not find evidencethat UV coloration of flanges is associated with nestling quality,parents preferentially fed young whose flanges reflected higherUV light, compared with experimentally UV-filtered nestlings.These results support the hypothesis that mouth coloration isa reliable signal of nestling condition. In addition, they showthat UV flange coloration influences parental decisions regardingfood allocation.     

Experimental food supplementation affects the physical development,behaviour and survival of Little Owl Athene noctua nestlings

In birds, energy supply during growth is a major predictor of the fledglings' physical condition and survival prospects. Differential quantity and quality of fledglings produced under varying nestling food supplies are likely to affect the number of offspring that recruit into the breeding population. However, the underlying mechanisms and associated consequences are still poorly known. Using a partial cross‐fostering and food supplementation experiment, we estimated the effect of variation in food supply during growth on nestling survival and fledgling phenotypic traits of Little Owls Athene noctua. Survival to fledging was much higher in food‐supplemented nestlings (98.6%) than in control nestlings (82.4%). Furthermore, supplemented nestlings were on average 8.9 g heavier and were more likely to develop subcutaneous fat deposits (99.4 vs. 73.7% of treatment and control nestlings, respectively). Supplemented nestlings also had on average longer wings than control nestlings, but tarsi and culmen did not differ significantly. Furthermore, experimentally supplemented fledglings struggled more when handled and emerged sooner from tonic immobility than control fledglings. The irises of supplemented fledglings were less intensely coloured. The experimentally induced changes in nestling development probably affect individual performance beyond fledging. Nestlings from orchard‐dominated habitats were larger than those from habitats dominated by arable land. As nestling food supply is largely determined by natural food availability, we conclude that habitat quality affects Little Owl productivity and offspring quality, and ultimately, population dynamics.     

Carotenoid-based nestling colouration and parental favouritism in the great tit

While elaborate carotenoid-based traits in adult birds may have evolved as honest signals of individual quality in the context of sexual selection or other social interactions, the function of carotenoid-based colours in juveniles is less well understood. We investigated the hypothesis that carotenoid-based nestling colouration has evolved in response to parental preference of intensely coloured offspring during food provisioning. In a field experiment, we manipulated nestling plumage colouration by a carotenoid-supplementation and analysed the parental food provisioning behaviour before feather appearance and at the end of the nestling stage. Carotenoids per se did not influence the nestlings begging behaviour or parental feeding decisions and we found no evidence that carotenoid-based colouration in nestling great tits has a signalling function in parent-offspring interactions. Parents did not discriminate between intensely coloured and control offspring in their food provisioning and in accordance with this finding intensely coloured nestlings were not heavier or larger at the end of the nestling stage. Alternative explanations for the evolution of carotenoid-based colours in nestling birds are discussed.     

Similarity in the begging calls of nestling Red‐winged Blackbirds

ABSTRACT Although individually distinct begging calls may permit parents to recognize their offspring, birds nesting in dense breeding colonies where fledglings intermingle might benefit from additional adaptations. For example, if the calls of all nestlings in a brood were similar, parents would need to recognize only one brood call instead of the identity calls of each nestling. We recorded nestling Red‐winged Blackbirds (Agelaius phoeniceus) to determine whether their calls function to identify individuals (identity call hypothesis) or broods (brood call hypothesis). We used spectrogram cross‐correlation and dynamic time warping as well as call duration, peak frequency, and frequency range to estimate the similarity of begging calls of nestling Red‐winged Blackbirds. We recorded individual nestlings on day 5 and on day 9 of the nestling period to determine whether calls of individuals were more similar than calls of different nestlings, and whether calls of broodmates were more similar than calls of nestlings from different broods. We found that calls of 8‐d‐old individuals were more similar than calls of different nestlings, but the calls of broodmates were not more similar than those of nestlings from different broods. These results were consistent with the identity call hypothesis. We then compared begging calls of pairs of nestlings recorded separately and together on day 9. We found that the calls of 8‐d‐old nestlings recorded together were more similar than when they were recorded separately. In addition, using playback of begging calls from normal broods and artificial “broods” constructed from the calls of single nestlings, we found that females returned with food sooner in response to the calls of single nestlings (with enhanced call similarity) than to those of normal broods. Our results suggest that similar begging calls may be beneficial for both nestlings and parents, with broodmates fed at higher rates when their calls are more similar and, after fledging, parents needing to recognize only one brood call instead of the identity calls of each fledgling.     

Parental allocation of food to nestling tree swallows: the influence of nestling behaviour, sex and paternity

Parents are expected to invest more in young that provide the greatest fitness returns. The cues that parents use to allocate resources between their offspring have received much recent attention. In birds, parents may use begging intensity, position in the nest or nestling size as cues to provision the most competitive young or those most likely to survive. It may also benefit parents to invest in young differentially by sex or relatedness if the fitness returns of sons and daughters differ or broods are sired by multiple males. We examined the allocation of food to tree swallow, Tachycineta bicolor, nestlings in relation to their begging behaviour, size, sex and paternity. Provisioning by parents was not related to nestling size, sex or paternity. The begging behaviour of nestlings did not differ with respect to sex or paternity. Both parents were more likely to feed nestlings that begged first or were closer to the nest entrance, suggesting that parents allocate food resources in response to cues that nestlings control. As a consequence, brood reduction was facilitated by biased provisioning within the brood in addition to the nestling size hierarchies created by hatching asynchrony. Copyright 2003 Published by Elsevier Science Ltd on behalf of The Association for the Study of Animal Behaviour.      

Acoustic signalling of hunger and thermal state by nestling tree swallows

The begging displays used by altricial nestling birds to solicit care from parents include vigorous movements and loud calling. These begging signals have attracted considerable interest, mainly because their intensity seems excessive for the function of transmitting information about nestling need to parents. However, how information on need is encoded in the various components of the signal, especially its acoustic components, is poorly understood. We examined how begging calls of large and small nestling tree swallows, Tachycineta bicolor, changed during a short period of food deprivation and cooling, as a first step in determining the role that various call characteristics played in advertising nestling need. In contrast to previous studies, we examined several call variables, and related them not only to need for food but also need for warmth. When nestlings were deprived of food, their calls increased in rate and length. Large nestlings also increased the amplitude of their calls. When nestlings were cooled during food deprivation, they decreased the frequency of their calls and their call rate. The latter trend was especially evident in small nestlings. Our results suggest that begging calls carry information not only on the overall hunger level of broods, as emphasized in previous studies, but also on the size, hunger and thermal need of individual nestlings. Further tests are needed to determine whether parents use this information and whether begging calls are optimally designed to convey it. Copyright 2001 The Association for the Study of Animal Behaviour.     

Parental Sex Differences in Food Allocation to Junior Brood Members as Mediated by Prey Size

Individual offspring within a brood may receive different amounts of provisioning from the male and female parents. Some hypotheses suggest that this bias is the result of an active and adaptive choice by parents. An alternative hypothesis is that feeding biases arise as a result of a constraint of fitting large prey items into small gapes. In an experiment with pied flycatchers, Ficedula hypoleuca , we tested for sex-biased allocation to junior nestlings in asynchronous broods and whether this could be explained by active parental choice or by passive allocation according to prey size and gape size. In both control broods and broods with experimentally increased degree of asynchrony, prey types did not differ between parents but females brought smaller prey than males at younger but not older nestling stages. At younger but not older nestling stages, the majority of feeds to junior nestlings were from females, and the smaller nestlings consumed smaller prey than older siblings. However, there was no evidence of active preference of small nestlings by females as parents did not differ in the tendency to bypass a begging senior nestling in order to feed a junior nestling. Provisioning rates by females were lower than those by males when nestlings were young and we suggest that foraging time constraints caused by the need to brood offspring result in females bringing smaller prey than males. In turn, the larger prey brought by males was more often transferred to larger offspring after the smaller ones failed to swallow it. In such cases, 'preferential' feeding of small nestlings by females may simply be a passive side effect of foraging constraints and gape-size limitations.     

Intraseasonal effects of clutch manipulation on parental provisioning and residual reproductive value of eastern phoebes (Sayornis phoebe)

Summary First clutches of double-brooded eastern phoebes Sayornis phoebe were manipulated (up two eggs, down 2 eggs or no change) to test for intraseasonal reproductive tradeoffs and to test whether size of first brood influenced food delivery rates to nestlings and nestling quality in second broods.Considering all nests from both broods, rate of feeding nestlings increased linearly with brood size but nestling mass per nest decreased with increasing brood size. High nestling weights in small broods may have resulted from parents delivering better quality food, but we did not test this.Among treatment groups in first broods, nestlings from decreased broods weighed more than those in control or increased broods. Treatment did not influence the likelihood that second nests would be attempted after successful first nests nor did it alter the interval between nests. Nestlings of parents that renested weighed more than those of parents that did not, regardless of treatment, suggesting that post-fledging care may preclude renesting. Mass of individual females did not change between broods, regardless of brood size. Clutch sizes of second attempts were not affected by manipulations of first broods but increasing first broods reduced the number of nestlings parents were able to raise to day 11 in their second broods. However, manipulation of first broods did not affect mean nestling mass per nest of nestlings that survived to day 11.In phoebes, parents of small first broods are able to raise nestlings in better condition. We predict that in harsh years, parents of small first broods would be more likely to renest. Parents of enlarged first broods sacrificed quality of offspring in second broods, which seems a reasonable strategy if nestlings from second broods have lower reproductive value.     

Features of begging calls reveal general condition and need of food of barn swallow (Hirundo rustica) nestlings

Altricial offspring of birds solicit food provisioning by complexbegging displays, implying acoustic and visual signals. Differentcomponents of begging behavior may function as reliable signalsof offspring state and thus reproductive value, on which parentsbase optimal parental decisions about allocation of criticalresources (e.g., food). We experimentally manipulated componentsof general condition of nestling barn swallows (Hirundo rustica)by (1) altering brood size by cross-fostering an unbalanced number of nestlings between pairs of synchronous broods andthus manipulating the level of within-brood competition forfood, (2) injecting some nestlings with a harmless immunogen,simulating an infection, and (3) preventing part of the nestlingsfrom receiving food for a short period while establishing controlgroups. We recorded rate of begging response by individual nestlings as parents visited the nest and recorded begging calls usinga DAT recorder to analyze six sonagraphic features of vocalizations.Our factorial experiment revealed that nestlings deprived offood begged more frequently when parents visited the nest comparedto their non—food-deprived nest mates. Food deprivationincreased duration of syllables forming begging calls, whereas brood size enlargement resulted in increased latency of responseto parental calls. Heavy nestlings in good body condition vocalizedat a relatively low peak frequency. To our knowledge, thisis the first study in which begging rate and sonagraphic structureof begging calls are shown to reliably reveal a diverse setof components of offspring general state, on which parental decisions may be based.     

Brood size manipulations reveal relationships among physiological performance,body condition and plumage colour in Northern Flicker Colaptes auratus nestlings

Visual signals of quality in offspring, such as plumage colour, should honestly advertise need and/or body condition, but links between nutritional status, physiological performance and the expression of colours are complex and poorly understood. We assess how food stress during rearing affected two physiological measures (T‐cell‐mediated immune function and corticosterone level in feathers: CORT_f) and how these two variables were related to carotenoid and melanin coloration in Northern Flicker Colaptes auratus nestlings. We were also interested in how these two physiological measures were influenced by the sex of the nestling. We experimentally manipulated brood size to alter levels of food availability to nestlings during development. We measured carotenoid‐based colour (chroma and brightness) in wing feathers and the size of melanin spots on breast feathers. In agreement with our prediction, nestlings in the reduced brood treatment had better body condition and stronger immune responses than those in the control and brood enlargement treatments. This supports the hypothesis that immune responses are energetically costly. In contrast, CORT_f was not related to nestling body condition or sex and was unaffected by brood size manipulation. Nestlings of both sexes with stronger T‐cell‐mediated immune responses had larger melanin spots but only males with higher immune responses also had brighter flight feathers. Feather brightness decreased with increasing CORT_f levels. Our study is one of the few to examine the relationship between multiple physiological and plumage measures in nestlings and shows that plumage colour and immune function signalled body condition of nestlings, but that feather corticosterone levels did not.     

Parental versus offspring control on food division within the brood: the role of hatching asynchrony

Using an individual-based simulation model we study how different mechanisms of food division among multiple offspring influence nestling number and quality, as well as parental effort. We consider the combination of different scenarios of food availability (feeding conditions), hatching asynchrony and food division. If parents have full control on how to divide food among offspring, asynchronous broods have higher breeding performance than synchronous ones in a wide range of feeding conditions, giving theoretical support to empirically proved benefits of hatching asynchrony. If parents accept the outcome of sibling competition there is a threshold in feeding conditions below which asynchronous broods produced more fledglings and the reverse was true above the threshold. Interestingly, parents relying on the outcome of nestling competition do not necessarily differ in breeding performance from those which have full control over food allocation. Our study combines hatching asynchrony, provisioning behaviour of parents, jostling behaviour of nestlings and feeding conditions as a network of interacting processes of enormous interest to fully understand the parent–offspring conflict.     

Complex feeding behaviour by magpies in nests with great spotted cuckoo nestlings

Parent decisions about food allocation are usually based on simple time‐saving rules that optimize their own fitness; however, they can sometimes vary depending on the prevailing ecological conditions both outside and inside the nest. Parent–offspring interactions also become more complex when parents suffer from brood parasitism, which implies that they care for the parasite's eggs and unrelated young. The great spotted cuckoo Clamator glandarius is a specialist brood parasite that uses the magpie Pica pica as its primary host. Here, by filming food allocation by magpie parents in natural non‐parasitized and experimentally parasitized and non‐parasitized magpie nests, we have found that magpie provisioning behaviour is highly complex including two types of feedings apart from normal ones. First, false feedings, when the parent touched the chick's beak but did not leave any food, occurred more frequently when feeding a cuckoo than when feeding magpie nestlings. Second, two types of what we have called coax feedings: 2a) when magpie parents induce a nestling to beg by waking it up by touching it softly with the beak, and 2b) when parents disregard begging signals (always from brood parasitic great spotted cuckoos) while coaxing one non‐begging nestling (always one of their own) to feed it. We suggest that brood parasitism, involving selfish excessively begging nestlings, could have acted as a selective pressure for both false and coax feedings to evolve, as both imply ignoring nestlings that beg too much. We also discuss that these parental responses could have evolved either by a discrimination without recognition mechanism, or, more probably, by a recognition‐based discrimination mechanism.     

Philornis infection in blue‐black grassquits: impact on nestlings and risk factors involved

Parasitic botfly larvae (Philornis ssp., Diptera: Muscidae) are found in nests of several bird taxa, although prevalence and impact on nestling survival vary considerably among species. Here we describe patterns of botfly infestation in blue‐black grassquit Volatinia jacarina nestlings. We identified the most typically affected nestling body parts and assessed parasite prevalence, impact on nestling survival, and changes in nestling body shape. Additionally, we tested whether climatic conditions, nest morphology and habitat characteristics are associated with larvae abundance. Blue‐black grassquits had low breeding success (16% of eggs/nestlings survived to fledged; 19% of the nests fledged at least one), but most failures resulted from predation by vertebrate predators. We estimated that 1% of nestlings died due to botfly infestation, and the number of subcutaneous larvae (range 1–18) in a nestling's body did not predict fledging success. Infected chicks exhibited higher tarsus asymmetry. Thus, we argue that although botflies had a small impact on offspring survival, they may reduce fitness in adulthood. There was no evidence that environmental conditions and nest morphology are linked to the number of larvae on nestlings. Nesting areas with higher food supply had lower infestation rates. Possibly, food‐rich habitats allow parents to invest more time in offspring care (brooding nestlings), thus protecting them from fly attacks. Alternatively, vegetation composition could influence local invertebrate diversity, which could provide a natural trophic buffer against adult Philornis. The present study brings to light new perspectives concerning bird–botfly interaction.     

Mouth colour components of begging are dynamic signals of quality in European starling nestlings

Offspring solicit food from their parents through begging signals. Nestling skin and flange coloration are begging signals that appear to convey information about nestling need or condition, and several experiments have shown that modifications of nestling coloration affect parental allocation decisions. However, it is important to examine the short‐term changes in these signalling components in response to food constraints since such dynamic changes are required for signals to indicate condition or need. Using a food deprivation experiment, we tested whether flange and skin reflectance in European starling Sturnus vulgaris nestlings change after a three‐hour interval. We investigated whether flange and skin reflectance changed according to the predictions arising from the ‘signal of quality’ or ‘signal of need’ hypotheses on the function of begging signals. We found that flange carotenoid and UV reflectance changed according to the signal of quality hypothesis with nestlings in good condition increasing their signal expression in response to the food deprivation, whereas those in poor condition decreased their signal expression. With the use of vision modelling, we show that changes in flange reflectance are detectable by starling parents. In contrast, we found a correlation going in the opposite direction for changes in skin UV reflectance. Nestlings with low lipid reserves increased their reflectance compared to nestlings with high reserves. However, vision modelling showed that short‐term changes in skin UV reflectance are not large enough to be detectable by the parents. Our study shows that flange carotenoid and UV reflectance are dynamic components of begging with short‐term variations that can be used by parents as signals of nestling quality.     

Nestling birds put their best flange forward

The offspring of caring parents may evolve specialized traits uniquely adaptive during their dependence on parental care. For example, the mouths of passerine nestlings are often bordered by enlarged and colorful rictal flanges expressed only during the nestling period. Although these traits are commonly hypothesized to act as visual signals during begging, non‐communication functions for the specialized mouth have been proposed as well. To test the hypothesis that nestling flange colors have evolved largely or exclusively as visual signals, I compared the reflectance of flange tissue that would be visible to parents during begging to that of flange tissue not exposed during begging in nestling house sparrows Passer domesticus and cliff swallows Petrochelidon pyrrhonota. Specifically, I tested the prediction that both condition‐dependent color parameters and those associated with visual conspicuousness would be expressed more intensely in tissue displayed during begging. Consistent with this prediction, flange tissue exposed during begging was brighter (reflected more total light), more UV‐rich, and had more intense carotenoid‐based coloration than hidden tissue. These differences do not exclude a non‐signaling function for flanges, but are consistent with the hypothesis that flange colors have evolved as visual signals.