Begging calls and parental feeding decisions in tree swallows (Tachycineta bicolor)

We conducted playback experiments to examine how parent tree swallows (Tachycineta bicolor) use nestling begging calls to distribute feedings to individuals within broods. In a first study, we used a paired-choice test to determine if parents discriminated between the taped begging calls of nestlings deprived of food and those of nestlings that had been recently fed. Our results showed that parents directed their first feeding attempt towards model nestlings near speakers playing deprived calls significantly more often than to models near speakers playing fed calls. They also made more feeding attempts overall to models with deprived calls. In the second study, we varied call rate and amplitude to examine which call features parents might use to discriminate begging calls. Parents directed significantly more first feeding attempts and more feeding attempts overall towards non-begging nestlings near speakers playing high call rates than to nestlings near speakers playing low call rates. They did not, however, discriminate between calls differing in amplitude. Previous studies have shown that parent birds use begging calls to regulate overall feeding rates to the brood. Our results suggest that parent tree swallows also use begging calls when feeding individual nestlings and, in particular, prefer calls associated with increased levels of nestling hunger. Received: 14 February 2000 / Revised: 6 October 2000 / Accepted: 16 October 2000     

Need and nestmates affect begging in tree swallows

We conducted an experiment on nestling tree swallows (Tachycineta bicolor) to examine predictions from signalling models for the evolution of conspicuous begging behaviour. Specifically, we examined the relationship between (1) nestling begging intensity and hunger, (2) begging intensity and parental provisioning and (3) begging intensity and nestmate condition. Forty broods of 9-day-old nestlings were removed from their nests for 1 h and assigned to one of the following three treatments: (1) all nestlings in the brood deprived of food (n = 13), (2) all nestlings in the brood fed (n = 11) or (3) half the nestlings in the brood deprived and half fed (n = 16). Videotapes before and after the treatments showed that begging intensity increased in broods in which all of the nestlings had been deprived and decreased in broods in which all of the nestlings had been fed. Deprived nestlings in the half-and-half treatment did not change their begging intensity in response to treatment, while fed nestlings in this treatment group showed a decrease in begging intensity. Parent tree swallows increased their feeding rate to deprived broods and decreased their rate to fed broods. Within broods, parents decreased their feeding rate to fed nestlings, but showed no significant change in feeding to deprived nestlings. Our results suggest that begging intensity is influenced by hunger and that parents appear to respond to variation in begging intensity. The begging of nestmates also appears to influence begging independently of need. These results are consistent with predictions derived from signalling models of begging. Received: 20 June 1997 / Accepted after revision: 19 January 1998     

Begging signals more than just short-term need: cryptic effects of brood size in the pied flycatcher (Ficedula hypoleuca)

The begging of nestling birds is known to reliably signal short-term nutritional need, which is used by parents to adjust rates of food delivery and patterns of food distribution within broods. To test whether begging signals reflect more than just short-term feeding history, we experimentally created 18 "small" (4-nestling) and 18 "large" (8-nestling) broods in the pied flycatcher (Ficedula hypoleuca). Compared to small broods, large broods were provisioned by parents at a greater rate, but at a lower visit rate per nestling and with no obvious differences in load mass per visit. However, lower rates of food mass delivery per nestling in large broods did not result in any measurable reduction in nestling growth (i.e. "long-term need") or in any increase in the begging effort per individual nestling whilst in the nest. Mid-way through the nestling period we also used hand-feeding laboratory trials to assess in more detail individual begging behaviour and digestive performance of the three mid-ranking nestlings from each brood. More food items were required at the start of each trial to satiate nestlings from large broods, but despite this initial control for "short-term need", nestlings from large broods went on to beg at consistently higher rates and at different acoustic frequencies. Large brood nestlings also produced smaller faecal sacs, which were quantitatively different in content but did not differ in frequency. We suggest that different nutritional histories can produce cryptic changes in nestling digestive function, and that these can lead to important differences in begging signals despite controlling for short term need.     

The role of posturing and calling in the begging display of nestling birds

Nestling birds produce a multicomponent begging display that has visual (e.g. posturing) and vocal (e.g. call rate) elements. Most work on the function of the display has focused on each component separately. However, understanding the evolution of complex displays such as begging requires knowledge of how the components function collectively. The purpose of our study was to determine how postural intensity and calling rate together influence parental feeding decisions in tree swallows, Tachycineta bicolor. We compared how begging components responded to a manipulation in which pairs of nestlings were either free to approach the parent when it arrived to feed (unconfined treatment) or confined to the back of their nestbox by a Plexiglass partition (confined treatment). We found no significant differences in postural intensity between treatments, but calling rate was significantly higher in the confined treatment. In both treatments, postural intensity, but not calling rate, correlated with hunger. Both components positively and independently correlated with the likelihood of a nestling being fed, although the correlation with postural intensity was stronger. Previous work suggested that both posture and call rate advertised hunger in nestling tree swallows. Here, call rate was not associated with hunger, but rather was affected by nestling position. These results suggest that calling may serve an additional role in helping nestlings in disadvantaged positions attract parental attention. The results also suggest that calling may have a complex relationship with hunger, position and nestmates.     

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.     

Nestling American robins compete with siblings by begging

Summary The evolution of intense begging by dependent nestling birds has recently been the subject of several theoretical papers. The interesting problem here is that nestlings should be able to communicate their nutritional status to parents in ways that are less costly energetically and less likely to attract predators. Thus, conspicuous begging behaviour is thought to have evolved as a result of either competition among nestmates or the manipulation of their parents to provide more food than would otherwise be favoured by selection. We studied sibling competition for parental feedings in the American robin (Turdus migratorius). We demonstrate that the probability that an individual nestling received food was related to several indices of begging. When we experimentally prevented parents from feeding part of their brood, both the intensity of begging and the number of feedings subsequently received by food-deprived nestlings increased. Furthermore, the begging intensity of those nestlings that were not food-deprived also increased in response to the begging of their hungrier siblings.Offprint requests to: R. Montgomerie     

Begging affects parental effort in the pied flycatcher, Ficedula hypoleuca

It has been suggested that nestlings use begging to increase their share of parental resources at the expense of current or future siblings. There is ample evidence that siblings compete over food with nestmates by begging, but only short-term effects of begging on parental provisioning rates have been shown. In this study, we use a new experimental design to demonstrate that pied flycatcher (Ficedula hypoleuca) nestlings that beg more are able to increase parental provisioning rates over the major part of the nestling period, thus potentially competing with future siblings. Parents were marked with microchips so that additional begging sounds could be played back when one of the parents visited the nest. By playing back begging sounds consistently at either male or female visits, a sex difference in provisioning rate that lasted for the major part of the nestling period was induced. If each parent independently adjusts its effort to the begging intensity of nestlings, begging may also be the proximate control mechanism for the sexual division of labour. Received: 24 January 1997 / Accepted after revision: 30 August 1997     

Food supply differentially affects sibling negotiation and competition in the barn owl (Tyto alba)

In contrast to most birds, nestling barn owls (Tyto alba) vocalise not only when parents are at the nest but also in their absence. Calls produced in their absence have been shown to facilitate sibling negotiation over the impending food resource. Since nestlings vocalise more vigorously in the presence of parents, they may be calling not to negotiate resources but to compete amongst each other over parental food distribution. A critical issue is to determine whether offspring need differentially affects sibling negotiation and sibling competition, that is vocalisation in the absence and presence of parents. To answer this question, I manipulated the food supply of 26 broods by adding or removing prey items. In the absence of parents, food-added broods vocalised at a significantly lower level than food-removed ones. In contrast, once a parent arrived at the nest, the vocalisation level was not significantly related to the manipulation of brood food supply. This suggests that in the absence of parents, it is more important for food-removed nestlings to vocalise intensely, and that in their presence, the relationship between begging and offspring need tends to vanish. In other words, brood food supply may affect sibling negotiation to a larger extent than sibling competition.     

Bioacoustic distances between the begging calls of brood parasites and their host species: a comparison of metrics and techniques

A variety of bioacoustics distance metrics have been used to assess similarities in the vocalizations of different individuals. Here, we provide a detailed analysis of several acoustic similarity indices, some of which have been developed with the specific aim of characterizing the sensory coding of auditory stimuli. We compare different approaches through the analysis of begging calls of several passerine species and specialist brood parasitic cuckoos that putatively evolved to mimic their hosts. The different bioacoustics distances did not provide consistently correlated similarity patterns, implying that they are sensitive to different sound features. However, the encoded spectrogram alignment method was correlated with all other acoustic distance metrics, suggesting that this method provides a consistent approach to use when the perceptually salient sound parameters are unknown for a particular species. Our analyses confirm that statistical similarity of begging calls can be detected in a New Zealand pair of host and specialist parasite species. We also show detectable similarity in two other Australasian host–parasite pairs and another New Zealand system, but to a more limited extent. By examining phylogenetic patterns in the begging call diversity, we also confirm that specialist cuckoos have evolved to mimic the begging calls of their hosts but host species have not co-evolved to modify their calls in response to begging call similarity by the parasite. Our results illustrate that understanding the function and mechanism of behavioral copying and mimicry requires statistically consistent measures of similarity that are related to both the physical aspects of the particular display and the sensory basis of its perception.     

Female mate choice in the gray treefrog (Hyla versicolor) in three experimental environments

We studied female mate choice by Hyla versicolor in three venues to examine how acoustic and spatial complexity, background noise, and the calling behavior of males might influence preferences manifest in previous laboratory two-stimulus choice tests. Our laboratory-based two-stimulus choice tests with and without broadcasts of chorus noise demonstrated that females prefer long calls relative to short calls when calling efforts of alternatives are equivalent. Background noise impaired the ability of females to discriminate in favor of longer over shorter calls, but the magnitude of the effect was small. Captures of females at eight speakers broadcasting 6- to 27-pulse calls at the edge of a pond revealed strong discrimination against only the shortest call variant. In natural choruses, females may only rarely encounter males using such unattractive vocalizations. Female phonotaxis at an artificial pond with caged and electronically monitored calling males also indicated that consequences of female preferences for temporal aspects of calling observed in two-stimulus choice tests are much attenuated in choruses and explain only small portions (<10%) of the variation in male mating success. Nevertheless, relatively high call duration and calling effort increased male attractiveness. Acoustic interference emerged as another significant factor influencing male mating success and possibly the differences in female choice observed in laboratory and chorus settings. We suggest that the bias of females against both overlapped and very short calls may help explain why males lengthen their calls but lower their rate of delivery in response to increases in chorus size.     

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.     

The effect of pup vocalisations on food allocation in a cooperative mammal, the meerkat (Suricata suricatta)

In the meerkat (Suricata suricatta), a cooperative mongoose, pups follow potential feeders while the group is foraging and emit incessant calls when soliciting food from them. In contrast to a ’stationary’ brood of chicks, in which nestlings are fed at a fixed location, meerkat pups are ’mobile’ and become spread out. The question arises whether meerkat pups that experience different constraints to those facing chicks have evolved similar begging strategies. This paper describes the vocalisations that meerkat pups emit in the context of begging and investigates the influence of these calls on food allocation by older group members and on the behaviour of littermates. Meerkat pups use two types of calls when soliciting food from a potential feeder. The most common is a ’repeat’ call, which pups emit continuously when following an older forager over several hours a day. In addition, when a potential feeder finds a prey item, the pups next to it emit a bout of calls with increased calling rate, amplitude and fundamental frequency, termed ’high-pitched’ calls. Observations, together with playback experiments, showed that more prey was allocated to pups that called longer and more intensely. The pup closest to a feeder was almost always fed. The probability of emitting high-pitched calls did not depend on the time since a pup had received food, and the change from repeat to high-pitched calls occurred suddenly. The main function of the high-pitched call, therefore, does not appear to be to signal a pup’s hunger state. More likely, the two calls, in the context of begging, may be an adaptation to energetic constraints in a mobile feeding system. Pups, which are dispersed during foraging, may emit repeat calls over long periods to prevent potential feeders from eating all the prey themselves. At the moment a potential feeder finds prey, pups may give the more intense high-pitched calls to direct feeders to bring the food item to them and not to a littermate. Therefore, unlike the stationary feeding system where chicks emit one type of begging call when the feeder approaches the nest, meerkats, with a mobile feeding system, have evolved two discrete types of vocalisations in the context of begging. Received: 22 November 1999 / Revised: 1 July 2000 / Accepted: 17 July 2000     

The importance of nestling location for obtaining food in open cup-nests

Observations and experiments were carried out at 34 four-nestling nests of Arabian babblers (Turdoides squamiceps) and feeding events were analyzed according to hatching order and nestling location in the nest. Nestlings were fed in a negative correlation with hatching order. Nestling locations in relation to the provisioners were defined as Near, Far, Right, Left, and Center. Feeders fed closer nestlings more often than those further away, and straight ahead rather than sideways. In the open circular nest, the feeding adults' positions were unpredictable and equally distributed around the nest. Each peripheral position therefore served equally as Near, Far, Right and Left positions. The Center was independent of the arrival direction of the feeders and was advantageous relative to the peripheral positions. The importance of the central position was demonstrated by three experiments. (a) Food deprivation for 1 h caused the first-hatched nestling to occupy the center position and gain more feedings than its siblings. (b) Introduction of a Perspex barrier into the nest, thus eliminating the central position and preventing the nestlings from changing places, led to a loss of importance of hatching order and equal provisioning of the nestlings. (c) Fencing the nest so that entry was possible from only one permanent direction, resulted in the first-hatched nestling occupying the near position more often than its nestmates and obtaining 52% of the feedings provisioned to the whole brood. These findings imply that the architecture of the nest has an important role in food distribution among the nestlings, and contributes to reducing inequalities in the siblings' abilities to obtain food.     

Begging behavior and food acquisition by brown-headed cowbird nestlings

Understanding the selective forces that limit the exaggeration of begging signals is a critical issue in understanding the evolution of begging behavior. I studied the begging behavior of nestlings of the brown-headed cowbird (Molothrus ater), a brood parasite. In the nests of indigo buntings (Passerina cyanea), brown-headed cowbird nestlings received approximately twice as much food per hour than their host nestmates. I tested three hypotheses for the mechanism by which cowbirds acquired more food than their bunting nestmates: the size advantage hypothesis, the signal exaggeration hypothesis, and the novel begging behavior hypothesis. I found support for the hypotheses that cowbirds acquire more food as a result of their larger body size, and due to the exaggeration of begging signals that are not dependent on body size. I did not find support for the role of novel begging behaviors in cowbird food acquisition. These results suggest that food acquisition by host chicks in unparasitized nests could be increased by the exaggeration of begging signals. Recent work suggests that such exaggeration may be limited by the risk of nest predation, but further studies are needed. Received: 12 December 1997 / Accepted after revision: 29 December 1997     

Parent-absent begging in the Brown-headed Cowbird (<Emphasis Type="Italic">Molothrus ater</Emphasis>): the role of short-term need and nestmate size

Although it is well-established that nestlings of many altricial species beg when parents are away from the nest, we have a poor understanding of parent-absent begging in brood parasites, including the proximate factors that may influence begging frequency and intensity. In this study, I examined how parent-absent begging was influenced by competitive asymmetries between host and Brown-headed Cowbird (Molothrus ater) nestlings under disparate levels of short-term need. Food-deprived cowbird nestlings begged more frequently and for a greater proportion of parent-absent period than when food-supplemented, with similar patterns observed in hosts of different sizes. In contrast, three metrics of cowbird begging intensity varied relative to host size but not due to differences in short-term need. Cowbirds consistently begged more frequently and intensively than host nestlings for a given level of short-term need, providing evidence that cowbird begging displays are more frequent and intense than non-parasitic nestlings during both feeding visits and parent-absent periods. In sum, the frequency of begging by cowbirds was only influenced by short-term need, whereas begging intensity during parent-absent events was only influenced by the host against which cowbirds competed. This study demonstrates that host size and short-term need had differing influences on the frequency and intensity of parent-absent begging in cowbirds, although both factors are likely important in limiting the evolution of parent-absent begging in cowbirds. Because it appears to provide no immediate benefits yet may decrease fitness, parent-absent begging should be included in future theoretical models investigating the evolution of begging displays in nestling birds.     

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.     

Provisioning rules in tree swallows

Conflict between parents and offspring may result in offspring exaggerating their needs and parents devaluing their begging signals. To determine whether this occurs, it is first necessary to establish the link between need, begging and parental response. The purpose of our study was to examine these relationships in tree swallows (Tachycineta bicolor). Parents preferentially fed nestlings that begged sooner, reached higher and were closer to the front of the nestbox (Fig. 1). Begging intensity of both individuals and entire broods increased with relatively long periods between feeding visits. Within broods, parents responded to increased begging intensity by increasing their feeding rate, although this effect was relatively weak. Large and small nestlings did not differ in their begging behavior and all nestlings, regardless of size, were fed at similar rates. Despite the overall equity in feeding, male parents preferentially fed larger nestlings while female parents fed smaller nestlings. Nestlings did not increase their begging intensity in response to begging by nestmates. Our results suggest that begging is related to need in this species and that parents respond to variation in begging intensity. Received: 4 May 1995/Accepted after revision: 17 December 1995     

Is obligate siblicidal aggression food sensitive?

In avian species whose chicks show facultative siblicide, attacks increase with food deprivation. In species that show obligate siblicide, this causal relationship is not expected, but no test has been made. When we composed artificial pairs of young brown boobies, Sula leucogaster (an obligately siblicidal species), and supplied variable amounts of food to the older nestlings in each pair, food ingestion was related to the most intense form of attack, pushes, which can cause death by expelling the broodmate from the nest. The less food an older nestling ingested, the more time it spent active and the greater its rate and absolute frequency of pushes, and the more often it expelled its nestmate. Hence, deficient food provision to older nestlings could precipitate siblicidal expulsion of broodmates. Younger nestmates were aggressive too, and the more they were pushed and expelled, the more they pecked. Aggression of senior brown-booby broodmates may be flexible and food sensitive in order to optimize the timing of siblicide or to make siblicide weakly facultative.Communicated by R. Gibson     

Heart rate changes reveal that little blue penguin chicks (Eudyptula minor) can use vocal signatures to discriminate familiar from unfamiliar chicks

Researchers investigating social recognition typically measure only behavioural responses during discrimination tests - physiological changes have been largely ignored. We examined whether little blue penguin chicks (Eudyptula minor) could distinguish siblings from other chicks using auditory cues, by measuring behavioural and heart rate changes during playback experiments. Chicks were exposed to five treatments: the begging calls of siblings, neighbouring chicks and unfamiliar chicks, and two controls (heterospecific begging calls and music). We also determined if chicks developed distinctive begging calls, by using F-ratios to quantify inter- versus intra-individual variability in a range of acoustic parameters, and applying a discriminant-function analysis. Inter-individual variation was greater for pitch than for temporal or amplitude parameters, suggesting that call pitch may be important for individual recognition. The discriminant-function analysis showed each chick's calls were distinctive and could act as a vocal signature. Treatments did not instigate different behavioural responses. However, chick heart rates during playback of sibling calls were significantly higher than those recorded during stranger, but not neighbour, playback. A simple recognition system based on familiarity may allow this plesiomorphic and loosely colonial penguin to gain at least some of the benefits associated with more advanced sibling recognition systems (some highly colonial seabirds discriminate siblings from neighbouring chicks). Heart rate could be a useful measure of social recognition abilities, particularly in species where changes in behaviour are not always evident or are difficult to observe.     

American robin nestlings compete by jockeying for position

Summary We investigated whether nestling American robins (Turdus migratorius) were capable of influencing food distribution in their nests by perceiving that certain sectors of the nest received a relatively high proportion of feedings and positioning themselves accordingly. Feeding observations were obtained from videotape recordings taken at different stages of the nestling period. Parents generally arrived at a predictable location on the nest rim and allocated proportionally more food to nestlings in the central position. The degree of nestling movement was significantly positively correlated with variation in the predictability of parental arrival locations on the nest rim. Furthermore, nestlings moved more in broods suffering brood reduction. This suggests that when competition for food is intense and the location of parental arrival is predictable, nestlings respond by jockeying for access to the most favorable (i.e., central) position in the nest. We conclude that jockeying for position by nestlings can influence the pattern of food allocation by parents, and that hungry nestlings can improve their competitive standing against nestmates by moving to positions where parents are more likely to feed them. Correspondence to: S.B. McRae