Nestling testosterone is associated with begging behaviour and fledging success in the pied flycatcher, Ficedula hypoleuca

Animal signals are hypothesized to be costly in order to honestly reflect individual quality. Offspring solicitation signals given by nestling birds are thought to have evolved to advertise either need or individual quality. We tested the potential role of testosterone (T) in controlling the intensity of these signals by measuring begging behaviour as: (i) duration of the begging display and (ii) maximum height of the begging stretch, and by sampling endogenous T levels in nestling blood. We tested nestling pied flycatchers (Ficedula hypoleuca) using well-established experimental paradigm involving transient food deprivation to encourage begging behaviour and then blood-sampled nestlings at the end of these tests for T levels. Our results show that individual nestlings with the most intense begging displays had the highest circulating levels of T immediately after testing. In addition, we found substantial differences between broods in terms of circulating T. Finally, we found evidence that broods with higher levels of T showed increased fledging success, indicating a benefit for increased T production in nestlings. The potential trade-offs involved in T-mediated begging behaviour are discussed.     

Does testosterone mediate the trade-off between nestling begging and growth in the canary (Serinus canaria)?

Nestling birds solicit food from their parents with vigorous begging displays, involving posturing, jostling and calling. In some species, such as canaries, begging is especially costly because it causes a trade off against nestling growth. Fitness costs of begging like this are predicted by evolutionary theory because they function to resolve conflicts of interest within the family over the provision of parental investment. However, the mechanism that links these costs with nestling behaviour remains unclear. In the present study, we determine if the relationships between nestling androgen levels, nestling begging intensities and nestling growth rates are consistent with the hypothesis that testosterone is responsible for the trade-off between begging and growth. We test this idea with a correlational study, using fecal androgens as a non-invasive method for assaying nestling androgen levels. Our results show that fecal androgen levels are positively correlated with nestling begging intensity, and reveal marked family differences in each trait. Furthermore, changes in fecal androgen levels between 5 and 8 days after hatching are positively associated with changes in nestling begging intensity, and negatively associated with nestling growth during this time. Although these correlational results support our predictions, we suggest that that experimental manipulations are now required to test the direct or indirect role of testosterone in mediating the trade-off between begging and growth.     

Nest predation and the evolution of nestling begging calls

Begging by nestling birds can be conspicuous and loud. Such displays are thought to function in signalling nestling condition and securing parental care, but they also may inadvertently attract the attention of predators. We compared the structure of nestling begging calls to the risk of predation among 24 species of birds breeding in a forest community in central Arizona. After controlling for body size and phylogeny, we found that species subject to greater nest predation had calls with higher frequency (pitch) and lower amplitude (loudness) than species subject to lower rates of nest predation. As these acoustic features make it difficult for potential predators to pinpoint the source of a sound, our results suggest that an increased risk of predation has led to the evolution of begging calls that minimize locatability. The relationship between call structure and the risk of predation also supports the hypothesis that attracting predators is a direct cost of begging and that such costs can constrain any evolutionary escalation in the intensity of nestling begging.     

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.     

Nestling colouration is adjusted to parent visual performance in altricial birds

Hitherto, most of the investigation on the perceptual efficacy of begging signals has dwelled on how patterns of nestling colouration adjust to predominant nest luminosity. However, visual sensitivity of birds varies across species, which raises the question of whether colouration of traits involved in begging displays is adjusted to parent visual capacities. Here, by comparing nestling colouration and visual sensitivity across 22 altricial bird species, we provide a first test of this hypothesis. Firstly, we assessed differences in performance of typical UV‐tuned and violet‐tuned bird eyes when looking at the nestling traits under the light regimes prevailing at their nests. Secondly, while controlling for common ancestry in a comparative approach, we explored variation in colouration of nestlings in relation to parent visual system. The colour discrimination model indicated a general higher performance of the ultraviolet over the violet eye at detecting gape and body skin traits in either open‐ or hole‐nest light conditions. Gape colouration was associated with parental visual system as the nestlings of UVS species displayed more yellow and less pure ultraviolet mouths than the nestlings of VS species. Thus, our results agree with an adaptive parent–offspring communication scenario where the nestlings’ colours tuned the perception capacities of their parents.     

Condition-dependent effects of corticosterone on a carotenoid-based begging signal in house sparrows

Begging is a complex display involving a variety of different visual and auditory signals. Parents are thought to use these signals to adjust their investment in food provisioning. The mechanisms that ensure the honesty of begging displays as indicators of need have been recently investigated. It has been shown that levels of corticosterone (Cort), the hormone released during the stress response, increase during food shortage and are associated with an increased begging rate. In a recent study in house sparrows, although exogenous Cort increased begging rate, parents did not accordingly adjust their provisioning rate. Here, we tested the hypothesis that Cort might affect the expression of other components of begging displays, such as flange color (a carotenoid-based trait). We experimentally increased levels of circulating Cort and investigated the effects of the treatment on (1) the flange coloration of the nestlings, (2) the behavioral response and (3) the parental allocation of food and (4) nestling condition and cell-mediated immune response. We found that Cort affected flange coloration in a condition-dependent way. Cort-injected nestlings had less yellow flanges than controls only when in poor body condition. Parental feeding rate was also affected by the Cort treatment in interaction with flange color. Feeding rate of Cort-injected nestlings was negatively and significantly correlated with flange color (nestlings with yellower flanges receiving more food), whereas feeding rate and flange color were not correlated in control chicks. We also found that nestlings injected with Cort showed a weaker immune response than controls. These results suggest that, indeed, Cort has the potential to affect multiple components of the begging display. As Cort levels naturally raise during fasting, parents have to take into account these multiple components to take a decision as to optimally share their investment among competing nestlings.     

Effects of feeding frequency on nestling begging and digestion

Nestling begging has the potential to provide parents with honest information about both short- and long-term nutritional needs, yet the importance of previous feeding experience remains largely untested in empirical studies. We examined the effect of two experimental feeding rates on nestling begging in Southern Grey Shrikes Lanius meridionalis using differences in load size to equalize the total volume of food received. There was variation in the pattern of begging behaviour between six pairs of siblings during a hand-feeding trial, although individuals maintained a similar begging intensity throughout a 9-h feeding period. Both treatment groups showed elevated begging responses during a terminal deprivation period, but nestlings fed small food items at frequent intervals demonstrated higher begging responses after a period of deprivation than did siblings fed large food items infrequently. As nestlings fed frequently with small food items had greater levels of undigested protein present in their faeces than birds fed large items infrequently, we suggest experimentally induced variation in digestive efficiency may account for the observed differences in begging behaviour. The possible role of learning, the adaptive significance of trade-offs between feeding rate and digestive efficiency, and a possible conflict of interests between parents and offspring are discussed.     

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.     

Effects of elevated yolk androgens on perinatal begging behavior in yellow-legged gull (Larus michahellis) chicks

Maternal hormones may represent an important pathway by which mothers can adaptively adjust offspring traits and performance to suit the prevailing environmental conditions. Earlier studies of birds have shown that egg androgens of maternal origin may enhance post-natal offspring 'begging' displays, functioning to solicit parental care. Here we investigate the effects of elevated egg androgen levels on the prenatal begging behavior of yellow-legged gull (Larus michahellis) chicks. At laying, we experimentally increased the concentration of yolk testosterone (T) within the natural range of variation, and, shortly before hatching, we compared the structural properties, rate, and loudness of vocalizations of embryos developing in T- and oil-injected (control) eggs. In addition, we compared the early post-hatch begging rate (measured as the pecking rate towards a dummy gull head) in chicks of the two experimental groups. We found that T embryos produced louder embryonic vocalizations than controls, whereas structural properties and the calling rate did not differ between T and control embryos. The post-hatch begging rate was unaffected by T treatment, but strongly decreased with increasing chick body mass, suggesting that intensity of the begging display was sensitive to chick state and may therefore reliably indicate the need of food in this species. Therefore, the results of this study show for the first time that prenatal T exposure modulates the quality of embryonic vocalizations, but are not in accordance with previous findings reporting increased post-hatching begging intensity following increased prenatal exposure to androgens.     

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.     

Reliable Information Content and Ontogenetic Shift in Begging Calls of Grey Warbler Nestlings

The most critical assumption of communication models regarding parent–offspring conflict is that food solicitation displays of genetic offspring are honest signals to elicit beneficial parental care. A critical requirement of honesty is the reliable change of perceivable aspects of begging calls with physiological needs. We experimentally tested whether and how the acoustic structure and begging call rate of individual Grey Warbler Gerygone igata nestlings change with hunger level and age. We also examined a rarely documented component of chick begging calls, namely the temporal dynamics of acoustic modulation after nestlings heard parental feeding calls. Begging call structure narrowed in frequency range and, surprisingly, decreased in amplitude as chick hunger levels increased. We also found that begging calls changed with chick age, with the frequency increasing and the duration decreasing for older chicks. These results indicate that the acoustic properties of nestling Grey Warbler begging calls are complex and may be used to signal several aspects of nestling traits, including hunger level and age (or size, a correlate of age). Overall, begging calls of Grey Warbler chicks appear to be honest, implying that parents are likely to benefit from relying on the acoustic features of their progeny’s calls which predict chick need. Our results have important implications regarding the reliability and information content of nestling solicitation signals for the brood parasite shining cuckoo Chrysococcyx lucidus exploiting Grey Warbler parental care, in that these begging‐call mimetic specialist cuckoos might also need to match closely the dynamics of acoustic features of their host chicks’ calls.     

Ambient noise and the design of begging signals

The apparent extravagance of begging displays is usually attributed to selection for features, such as loud calls, that make the signal costly and hence reliable. An alternative explanation, however, is that these design features are needed for effective signal transmission and reception. Here, we test the latter hypothesis by examining how the begging calls of tree swallow (Tachycineta bicolor) nestlings and the response to these calls by parents are affected by ambient noise. In a field study, we found that call length, amplitude and frequency range all increased with increasing noise levels at nests. In the laboratory, however, only call amplitude increased in response to the playback of noise to nestlings. In field playbacks to parents, similar levels of noise abolished parental preferences for higher call rates, but the preference was restored when call amplitude was increased to the level that nestlings had used in the laboratory study. Our results show that nestling birds, like other acoustic signallers, consistently increase call amplitude in response to ambient noise and this response appears to enhance discrimination by receivers. Thus, selection for signal efficacy may explain some of the seemingly extravagant features of begging displays.     

Calling at a cost: elevated nestling calling attracts predators to active nests

Begging by nestling birds has been used to test evolutionary models of signalling but theory has outstripped evidence. Eavesdropping predators potentially impose a cost on begging that ensures signal honesty, yet little experimental evidence exists for such a cost at active nests because the use of artificial nests, long playback bouts and absence of parents may have exaggerated costs. We broadcast short periods (1 h) of either nestling vocalizations or background noise at active white-browed scrubwren, Sericornis frontalis, nests. Nestlings called naturally during both treatments, allowing us to test whether elevated calling increases risk, a key but rarely tested assumption of evolutionary models. Predators visited nests exclusively during periods of elevated calling. Furthermore, playbacks affected neither adult visits nor nestling activity, suggesting that calling alone attracted predators. Adults gave alarm calls and nestlings usually called less when predators approached nests. Predation risk to broods is, therefore, likely to fluctuate substantially over short periods of time, depending on nestling hunger and whether adults or young have detected predators. This study confirms a present-day cost of nestling begging, demonstrates that this cost can be incurred over short periods and supports the importance of parent-offspring antipredator strategies in reducing predation risk.     

Age-Related Changes in Signalling of Need by Nestling Tree Swallows (Tachycineta bicolor)

Despite a large literature on the ontogeny of behaviour, few studies have examined how the function of juvenile behaviour changes during development. One of the most widespread and important juvenile behaviours is begging, the display used by young animals to solicit food from their parents. Begging signals generally vary reliably with offspring need for food and have served as models for understanding the evolution of honest signalling. Little is known, however, about whether the relationship between begging and need varies over the period of rapid juvenile development. Here, we examine whether tree swallow, Tachycineta bicolor, begging calls consistently reflect hunger levels across the 20 d nestling period. We recorded begging calls at 5, 10 and 15 d post‐hatch, during an hour of food deprivation, and related call features to time without food (i.e. hunger) at each age. The overall correlation between call structure and hunger, as measured by canonical correlation, was consistent across ages. The particular features that correlated with hunger varied, however. Call rate and length increased with hunger at all ages, but call amplitude and frequency range increased with hunger at days 10 and 15 only. The results of our study suggest that begging calls consistently convey information about offspring hunger throughout the nestling period, with the number of call features encoding hunger increasing with nestling age. This change may enhance the ability of parents to assess offspring hunger levels by adding redundancy to the signal.     

Benefits of Extra Begging Fail to Compensate for Immunological Costs in Southern Shrike (Lanius meridionalis) Nestlings

Theoretical models aimed at explaining the evolution of honest, informative begging signals employed by nestling birds to solicit food from their parents, require that dishonest signalers incur a net viability cost in order to prevent runaway escalation of signal intensity over evolutionary time. Previous attempts to determine such a cost empirically have identified two candidate physiological costs associated with exaggerated begging: a growth and an immunological cost. However, they failed to take into account the fact that those costs are potentially offset by the fact that nestlings that invest more in begging are also likely to obtain more food. In this study, we test experimentally whether a 25% increase in ingested food compensates for growth and immunological costs of extra begging in southern shrike (Lanius meridionalis) nestlings. Three nestmates matched by size were given three treatments: low begging, high begging-same food intake, and high begging-extra food intake. We found that, while a higher food intake did effectively compensate for the growth cost, it failed to compensate for the immunological cost, measured as T-cell mediated immune response against an innocuous mitogen. Thus, we show for the first time that escalated begging has an associated physiological net cost likely to affect nestling survival negatively.     

Food limitation in asynchronous bluethroat broods: effects on food distribution, nestling begging, and parental provisioning rules

Scramble competition models of begging predict that junior nestlingswill be more affected by food limitation than seniors. Thesemodels assume that food allocation is under offspring controland, hence, predict that this change in food distribution iscaused by a differential behavioral response by seniors andjuniors. By using the bluethroat (Luscinia svecica svecica)as our model species, we induced food limitation by removingthe male parent temporarily. We found that, as predicted, fooddistribution became more biased in disfavor of juniors whenfood was limited. However, there was no significant differencein the behavioral responses of seniors and juniors (i.e., positioningin the nest or begging postures) to food limitation that couldexplain the change in food distribution. Hence, there was noevidence that seniors controlled food distribution. As predictedif parents preferentially fed seniors, nestling rank affectedfood distribution when controlling for variation in nestlingbehaviors. Furthermore, as expected if the increased skew infood distribution under food limitation was caused by activefood allocation by parents, nestling rank had a greater effecton food distribution under food limitation than under normalconditions. The present study suggests that food distributionin passerine birds is determined not only by nestling behaviors(begging posture and positioning) alone but also by parentalpreferences for seniors based on nonsignaling cues, such asbody size.     

Manipulation of hunger levels affects great spotted cuckoo and magpie host nestlings differently

Brood parasitic nestlings usually exhibit an exaggerated begging behaviour, which is mainly attributed to reduced inclusive fitness costs since they typically share the nest with unrelated individuals. However, energetic costs also constrain begging expression and accordingly a relation between food requirements and intensity of begging behaviour could also exist in brood parasites, just as in nesting bird species. Here, we tested this hypothesis in the great spotted cuckoo Clamator glandarius and its main host, the magpie Pica pica, by studying the effect of an appetite enhancer, cyproheptadine hydrochloride, on nestling provisioning and development (size, body mass and cell‐mediated immune response). To study nestling provisioning, neck‐collars were meticulously placed around nestling necks allowing normal respiration but avoiding the ingestion of food delivered by adult magpies during ca 2.5 h. Loss in body mass during neck‐collar trials was used as a proxy for energetic begging costs, while the amount of food received during these trials and growth during the whole nestling period were used as variables reflecting short‐ and long‐term effects of the experimental treatment. During neck‐collar trials, we found that experimental nestlings of both species received more food than control nestlings. However, experimental magpies, but not cuckoos, lost more body mass than control nestlings. These results suggest a short‐term beneficial effect of an escalated begging behaviour in both species that would be energetically cheaper for cuckoos than for magpies. We found positive long‐term effects of the appetite enhancer only in magpies (in terms of tarsus and wing length at fledging, but not in terms of immune response and body mass); suggesting that exaggerated begging would be beneficial for hosts only. We discuss the possible effect of begging behaviour on the risk of predation and on inclusive fitness, but also the possibility that our results may be explained by some kind of limitation in the capability of food assimilation by parasitic species.     

Muting individual nestlings reduces parental foraging for the brood

Nestling birds use vocal and visual behaviours when soliciting food from parents. Such behaviours serve at least two discrete functions: (1) to induce parents to bring more food; and (2) to influence how food is allocated among brood members. Playback experiments have shown that vocalizations serve function 1. Do they also function to influence intrabrood allocation, as contemporary begging theory suggests, or is that governed chiefly by the nonvocal components of begging (neck stretching, gaping, jockeying for position within the nest)? We tested this hypothesis using a novel nonsurgical muting technique to decouple the vocal and visual components of begging in nestling red-winged blackbirds, Agelaius phoeniceus. Single chicks that were muted temporarily (1 h) continued to be fed at roughly the same rate as either the same individual prior to muting or sham-muted nestlings in the same brood. Parents reduced provisioning rates by increasing nest attentiveness in response to changes in the begging behaviour of the brood following treatment. These changes included less time spent begging (visual and vocal) accompanied by a reduction in the collective vocalizations of the brood. Our results suggest that vocalizations function primarily to regulate parental foraging rates, and visual begging displays function primarily to access food (competition).Copyright 2002 Published by Elsevier Science Ltd on behalf of The Association for the Study of Animal Behaviour     

Parent-offspring conflict and the coordination of siblings in gulls

Offspring solicit food from their parents by begging behaviours. Studies on birds suggest that these displays are 'honest signals of need' and adults provide food according to the begging level. However, siblings may compete for parental resources and the begging intensity is expected to change with brood size. Here, we show that in the black-headed gull (Larus ridibundus) an increase of the numbers of siblings can result in a decrease of individual begging cost through nestlings' synchronized signalling. This is in accordance with some mathematical models. As parents respond to the total solicitation emerging from the nest, the probability to get food increases with the number of chicks begging together. The more siblings there are, the more they coordinate their begging while decreasing the number of individual begging bouts. Intra-brood synchronization of begging enables chicks to reduce their effort and hence exerting an important role in parental-offspring negotiation.     

IBERIAN AZURE-WINGED MAGPIE CYANOPICA (CYANA) COOKI NESTLINGS BEGGING CALLS: CALL CHARACTERIZATION AND HUNGER SIGNALLING

ABSTRACT

Nestling begging behaviour has long been seen as a signal by which nestlings solicit care from parents and most of the existing evidence provides some support for it being an honest signal. Begging is a multicomponent signal in which both sound and vision components are usually important. Although it is known that begging encodes information about nestling hunger the present knowledge about the specific behavioural features that convey the information is still scarce. The aim of this study was to describe begging calls of Iberian Azure-winged Magpie Cyanopica (cyana) cooki nestlings and examine how information on nestling hunger might be encoded in the begging calls. Nestlings were experimentally submitted to different periods of food deprivation and the call variation within individuals was studied. The young were individually tested and stimulated to beg by simulating parental visits. When subject to increasing food deprivation periods, nestlings increased the response level to simulated parental visits. The study also found that for the studied size differences, nestlings did not differ in their response level. Results confirmed that information on nestlings' hunger might be encoded in parameters of the calling behaviour. When the food deprivation periods increased, nestlings tended to start begging earlier, begged more often, extended their calling bout and increased the call duration, changing both at the level of the call and vocal begging bout. Overall the results support the view of begging as an honest signal, namely that begging should reflect nestling hunger and that only some call features might encode information about hunger.