Begging in Common Redstart Nestlings: Scramble Competition or Signalling of Need?

Begging behaviour by the young affects parental food distribution among nestlings of altricial birds. We present an analysis of two types of begging behaviour (assuming the front nest positions and gaping) based on videotaped natural nestling feeding in European common redstart (Phoenicurus phoenicurus). We test whether these types of begging support the predictions of two mathematical models: scramble competition with competitive asymmetries between nestlings [Anim. Behav. 27 (1979) 1210] or honest signalling model [Nature 352 (1991) 328]. None of the measured variables of nestling or parental behaviour were affected by body weight differences between siblings. In contrast, both gaping and nest positioning were affected by individual differences in nestling hunger. In agreement with the honest signalling model, hungrier nestlings gaped with higher probability and started to gape sooner after the arrival of the parent than did their less hungry nestmates. Those nestlings with the shortest latency to gape also received food more often. Nest positioning was related to nestling hunger in a way unforeseen by the existing models. The intervals between nestling position changes were several times longer than the intervals between parental feeding visits, and parents preferred to feed nestlings in front positions, so nestlings in front positions were always less hungry than nestlings in back. Hence the pattern of movements influenced the feeding decision in favour of the more satiated nestlings and acted against the effect of gaping. Nestling movement seemed to be caused by the less hungry nestlings moving actively from front to rear positions. Low mortality of individual nestlings within broods that survived to fledging and small within‐brood variation in fledging weights indicated low competition among nestmates. We suggest that there are two behavioural mechanisms that contribute to the equalization of fledging weights in common redstart nestlings: the signalling of need through gaping and the regular turnover of nestlings at front positions.     

Brood size and begging intensity in nestling birds

Theoretical models suggest that sibling competition should selectfor conspicuous begging signals. If so, begging intensity mightbe expected to increase with the number of competitiors. Thepurpose of our study was to examine the relationship betweenbegging intensity and brood size using nestling tree swallows(Tachycineta bicolor) as our model. Over 2 years, we videotapedbegging behavior in unmanipulated broods of different sizes.We found that begging intensity increased with brood size. Theaverage weight of nestlings in each brood did not vary withbrood size, but feeding rate per nestling decreased with broodsize, suggesting that nestlings in larger broods begged moreintensively, possibly because they were hungrier. We also conductedan experiment to examine the effect of nest mates on beggingin different-sized broods. We found that nestlings with similarweights, previous competitive environments, and food deprivationbegged more intensively in large broods than in small broods.Overall, our study indicates that begging intensity increaseswith brood size in tree swallows. This relationship may resultfrom interactions among brood mates rather than from lower feeding rates to individual nestlings in larger broods.     

Adaptive developmental plasticity in growing nestlings: sibling competition induces differential gape growth

Sibling competition has been shown to affect overall growth rates in birds. However, growth consists on the coordinated development of a multitude of structures, and there is ample scope for developmental plasticity and trade-offs among these structures. We would expect that the growth of structures that are used in sibling competition, such as the gape of altricial nestlings, should be prioritized under intense competition. We conducted an experiment in the spotless starling (Sturnus unicolor), cross-fostering nestlings to nests with different levels of sibling competition. We predicted that nestlings subjected to higher levels of sibling competition should develop larger gapes than control birds. We found that, halfway through the nestling period, overall size (a composite index of mass, wing, tarsus and bill) was reduced in nests with intense sibling competition, whereas gape width remained unaffected. At the end of the nestling period, experimental nestlings had wider gapes than controls. Additionally, a correlative study showed that nestling gape width increased when feeding conditions worsened and overall size decreased. These patterns could either be due to increased growth of gape flanges or to delayed reabsorption of this structure. Our results show that birds can invest differentially in the development of organs during growth, and that the growth of organs used in sibling competition is prioritized over structural growth.     

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.     

Kind to kin: weak interference competition among white stork Ciconia ciconia broodmates

Altricial nestlings in structured families show a diverse array of behavioural mechanisms to compete for food, ranging from signalling scrambles to aggressive interference. Rates of filial infanticide are moderately high in white storks. It has been hypothesized that this unusual behaviour is an adaptive parental response to the absence of efficient mechanisms of brood reduction (aggression or direct physical interference) by nestlings. To test this latter assumption, we analyzed video recordings of 41 complete feeding episodes at 32 broods during the first half of the nestling period, when nestlings complete 90% of growth and chick mortality and size asymmetries are highest. Parents delivered food to all nestlings simultaneously by regurgitating on the nest floor. No direct (bill to bill) feeding was recorded. Senior nestlings were never observed to limit their junior nestlings from eating food, either by aggression or physical interference. Experimental feeding tests revealed that heavier nestlings handled prey items more efficiently and ate food at a higher speed. The high degree of tolerance shown by senior nestlings is unusual among birds with similar ecological and phylogenetic affinities, such as herons. Tolerance by seniors cannot be easily explained by absence of parental favouritism or proximate factors known to affect the occurrence of sibling aggression in other species (rate of food transfer, brood size, hatching asynchrony or length of nestling period).     

Reduced nestling growth of East African Stonechats Saxicola torquata axillaris in the presence of a predator

We investigated nestling growth of tropical East African Stonechats Saxicola torquata axillaris to evaluate the effects of nest predation, predator presence and food availability. We provided some Stonechat pairs with supplemental food, while others in a similar habitat served as a control. Concomitantly, we assessed the presence of Fiscal Shrikes Lanius collaris in supplemental fed and unsupplemented territories. Fiscal Shrikes prey on adult Stonechats and nestlings. We found that nestling growth was considerably reduced in Stonechat pairs that shared their territory with a Shrike. This effect was greater in nestlings of pairs that did not receive supplemental food. The reduction in nestling growth rates was significantly correlated with a reduced rate of visiting by the parents. Behavioural observations further suggested that parents reduced their feeding visits to the nest presumably to minimize their own predation risk, rather than predation risk of their brood. Our experiments show that the lower reproductive investment in tropical Stonechats can be attributed to risk-sensitive behaviour of the parents, especially when food is in limited supply.     

Food division in the Arabian babbler nest: adult choice or nestling competition?

Many studies have found that food division among nestmates isnegatively correlated with hatrhing order. The hypothesis thatfeedings are distributed according to the provisioners' selectionis compared here with the hypothesis that feedings are dividedas a consequence of nestling competition. Food distributionamong Arabian babbler nestmates was negatively correlated withhatching order and was so skewed that many last-hatched nestlingsdied as a consequence of starvation. No feeding preference wasfound between any adult and any given nestling. No differencewas found in feeding distribution among parents, partial parents,and nonparents. When an older foreign nestling was introducedinto the nest, adults fed the newcomer more intensively thantheir own offspring, implying that feeding division among nestmateswas not determined by die feeders but by the nestlings' relativeability to obtain food. In two-nestling nests, the older nestlingobtained 62% of the feedings, on average. However, followingselective feedings of the second-hatched nestling by the investigator,which equalized the two siblings' feeding amounts by the endof their second day, no difference was found between their feedingrates. The relative advantage of the older nestlings was eliminatedby introducing a barrier into the nest. Under these conditions,feedings were distributed equally among the nestmates. Sinceneither hatching order, previous priority order, nor individualidentification were used by the provisioning adults, the proximatefactor determining food division among the neslings appearsto be the result of nestling competition     

Begging in the absence of parents by nestling tree swallows

Begging by nestling passerine birds has become a model systemfor studies in animal communication. Although most beggingoccurs when parents arrive at the nest to feed (here called"primary begging"), it also occurs between feeding visits andimmediately after parents leave the nest. Begging in thesecontexts (here called "secondary begging") may have relativelylittle influence on the probability of receiving food, but could increase the overall cost of the signal and thus influence nestlingbegging strategies. The purpose of our study was to determinehow often tree swallow (Tachycineta bicolor) nestlings begin contexts other than to parents with food and to examinewhat factors influence the frequency of this begging. Secondarybegging ranged from 7% of measured begging responses at day2 to 30% by day 8 and was more frequent when the interval betweenparental feeding visits was relatively long and when the timeto respond to the arrival of parents with food was short. Increasesin both age and intervisit interval were associated with decreasesin nestling response times, suggesting that secondary beggingmay be related to the speed with which nestlings respond to stimuli. We discuss possible functions of secondary beggingand raise the possibility that it may, in fact, be an error.     

Behavior of adult and young grassland songbirds at fledging

The behavior of adults and young at the time of fledging is one of the least understood aspects of the breeding ecology of birds. Current hypotheses propose that fledging occurs either as a result of parent‐offspring conflict or nestling choice. We used video recordings to monitor the behavior of nestling and adult grassland songbirds at the time of fledging. We observed 525 nestlings from 166 nests of 15 bird species nesting in grasslands of Alberta, Canada, and Wisconsin, USA. Overall, 78% of nestlings used terrestrial locomotion for fledging and 22% used wing‐assisted locomotion. Species varied in propensity for using wing‐assisted locomotion when fledging, with nestling Grasshopper Sparrows (Ammodramus savannarum) and Henslow's Sparrows (Centronyx henslowii) often doing so (47% of fledgings) and nestling Song Sparrows (Melospiza melodia), Common Yellowthroats (Geothlypis trichas), and Chestnut‐collared Longspurs (Calcarius ornatus) rarely doing so (3.5% of fledgings). For 390 fledging events at 127 nests, camera placement allowed adults near nests to be observed. Of these, most young fledged (81.5%) when no adult was present at nests. Of 72 fledging events that occurred when an adult was either at or approaching a nest, 49 (68.1%) involved feeding. Of those 49 fledgings, 30 (62.1%) occurred when one or more nestlings jumped or ran from nests to be fed as an adult approached nests. The low probability of nestlings fledging while an adult was at nests, and the tendency of young to jump or run from nests when adults did approach nests with food minimize opportunities for parents to withhold food to motivate nestlings to fledge. These results suggest that the nestling choice hypothesis best explains fledging by nestlings of ground‐nesting grassland songbirds, and fledging results in families shifting from being place‐based to being mobile and spatially dispersed.     

Brood size, sibling competition, and the cost of begging in great tits (Parus major)

Evolutionary theory of parent-offspring conflict explains beggingdisplays of nestling birds as selfish attempts to influenceparental food allocation. Models predict that this conflictmay be resolved by honest signaling of offspring need to parents,or by competition among nestmates, leading to escalated beggingscrambles. Although the former type of models has been qualitativelysupported by experimental studies, the potential for a beggingcomponent driven by scramble competition cannot be excludedby the evidence. In a brood-size manipulation experiment withgreat tits, Parus major, we explored the scramble componentin the begging activity of great tit nestlings by investigatingthe mechanisms of sibling competition in relation to brood size.While under full parental compensation, the feeding rate pernestling will remain constant over all brood sizes for bothtypes of models; the scramble begging models alone predict anincrease in begging intensity with brood size, if begging costsdo not arise exclusively through predation. Great tit parentsadjusted feeding rates to brood size and fed nestlings at similarrates and with similar prey sizes in all three brood-size categories.Despite full parental compensation, the begging and food solicitationactivities increased with experimental brood size, whereas nestlingbody condition deteriorated. These findings support a scramblecomponent in begging and suggest that the competition-inducedcosts of food solicitation behavior play an important role inthe evolution of parent-offspring communication.     

Removal of a nest-mate elicits an age-dependent increase in plasma corticosterone of nestling Black-legged Kittiwakes

ABSTRACT.   Plasma corticosterone concentrations in birds often increase about 3 min after exposure to a stressor such as capture and handling. When measuring adrenal responsiveness of nestlings in broods with more than one nestling, standardizing capture protocols to equalize the stressor among nestlings if they simultaneously perceive the presence and activity of a researcher as a stressor is logistically difficult. The objective of our study was to determine if nestling Black-legged Kittiwakes ( Rissa tridactyla ) in broods of two mount a corticosterone response when the first nestling is removed from the nest or, alternatively, if each initiates a corticosterone response only at the time it is handled. We obtained blood samples from one nestling within 3 min of initial disturbance of the nest, and then removed and sampled its sibling 10 min later. For younger nestlings, we found no difference in corticosterone levels between those sampled at 3 min and their sibling sampled at 10 min. In contrast, older nestlings sampled at 10 min after initial nest disturbance had elevated corticosterone levels compared to those sampled within 3 min. In addition, nestlings sampled within 3 min of capture had elevated corticosterone when exposed to protracted periods of investigator disturbance at nearby nests. Our results suggest that it is necessary to treat initial disturbance of the nest as the onset of the stress response for all nestlings in multi-nestling broods when handling older nestlings or nestlings of unknown age. In addition, for species that nest in dense colonies, the presence of an investigator at one nest may be a stressor for nestlings in adjacent nests.     

Effect of altitude on male parental expenditure in Mountain Bluebirds ( Sialia currucoides ): are higher-altitude males more attentive fathers?

Male investment of time and energy in caring for offspring varies substantially both between and within bird species. Explaining this variation is of long-standing interest to ornithologists. One factor that may affect male care is breeding site altitude, through its effects on climate. The harsher, less predictable abiotic conditions at higher altitudes are hypothesized to favour increased male investment of time and energy in offspring care. We tested this hypothesis by comparing male parental behaviour in Mountain Bluebirds (Sialia currucoides) nesting at 1500 and 2500 m a.s.l. in the Bighorn Mountains of Wyoming, USA. We compared rates of prey delivery to nestlings at these two altitudes at two times: 1–2 days after hatching, when females spend much of their time brooding young, and 12–13 days later, when brooding has ended and nestling energy demands are peaking. High-altitude males fed nestlings 18 and 28% more often than low-altitude males early and later in the nestling stage, respectively, but only the difference in late-stage feeding rates were significant. Like males, females at the high site also fed nestlings significantly more often than females at the low site later in the nestling stage (45% difference in feeding rates). Consequently, the proportion of all feeding trips made by males at the high site (40%) did not differ significantly from that at the low site (44%). Parents at the high altitude may feed nestlings more often to compensate for their greater thermoregulatory costs. Parents may also be attempting to assist nestlings in storing fat and/or attaining a large size and effective homeothermy as quickly as possible to enhance nestling ability to survive bouts of severe weather which are common at high altitudes.     

Begging to differ: scrubwren nestlings beg to alarm calls and vocalize when parents are absent

Nestling birds face a dilemma: they can increase parental provisioning by begging more intensively, but by doing so may also increase their risk of predation. Nestlings could deal with this dilemma by reducing begging intensity after parents have warned them of a nearby predator. We therefore tested experimentally whether nestling scrubwrens, Sericornis frontalis, increase begging intensity with hunger but reduce it after adult alarm calls. Single 5- and 8-day-old nestlings were temporarily taken into the laboratory for playback experiments. Over a 90-min period of food deprivation we simulated parental visits every 10 min by playing back adult feeding calls. Hungrier nestlings begged louder and longer to simulated parental visits, but contrary to expectation did not beg less if they had previously heard playback of alarm calls, and even begged to the alarm calls themselves. The results were similar for both ‘mobbing’ and ‘flee’ alarm calls. Nestlings also gave distinctive calls in the 10-min interval between simulated parental visits, and the number of these calls increased with hunger and after playback of alarm calls. We suggest that nestlings acquire the ability to respond appropriately to alarm calls late in the nestling period and that therefore parents might be selected to avoid alarm calling when defending young nestlings.Copyright 2003 Published by Elsevier Science Ltd on behalf of The Association for the Study of Animal Behaviour.      

Perching of Tengmalm's Owl (Aegolius funereus) Nestlings at the Nest Box Entrance: Effect of Time of the Day,Age, Wing Length and Body Weight

The behaviour of the nestlings of nocturnal cavity-nesting species has relatively rarely been studied in detail because of problems connected with use of the technical devices required to provide long-term monitoring of individuals. However, long-term observation of nestling behaviour is crucial in order to identify different types of behaviour which may be caused by sibling competition at the end of nesting period. We studied behaviour of 43 Tengmalm''s owl (Aegolius funereus) nestlings at 14 nests using a camera and a chip system. The nestlings perched at the nest box entrance from an average age of 28 days from hatching (range 24–34 days) until fledging, spending around 2 hours per day here in total, in periods ranging from a few seconds to 147 min (7.6±10.9 min, mean ± SD). We found that individual duration of perching at the nest box entrance was significantly influenced by nestlings'' age and wing length and that the duration of perching at the nest box entrance significantly decreased with time of night. However, during daylight hours, time of day had no effect on either probability or duration of nestlings'' perching. We suggest daylight perching at the nest box entrance results from nestlings'' preparation for fledging, while individuals perching here during the night may gain an advantageous position for obtaining food from the parents; another possibility at all times of day is that nestlings can reaffirm their social dominance status by monopolizing the nest box entrance.     

Supplementary feeding increases nestling feather corticosterone early in the breeding season in house sparrows

Several studies on birds have proposed that a lack of invertebrate prey in urbanized areas could be the main cause for generally lower levels of breeding success compared to rural habitats. Previous work on house sparrows Passer domesticus found that supplemental feeding in urbanized areas increased breeding success but did not contribute to population growth. Here, we hypothesize that supplementary feeding allows house sparrows to achieve higher breeding success but at the cost of lower nestling quality. As abundant food supplies may permit both high‐ and low‐quality nestlings to survive, we also predict that within‐brood variation in proxies of nestling quality would be larger for supplemental food broods than for unfed broods. As proxies of nestling quality, we considered feather corticosterone (CORT_f), body condition (scaled mass index, SMI), and tarsus‐based fluctuating asymmetry (FA). Our hypothesis was only partially supported as we did not find an overall effect of food supplementation on FA or SMI. Rather, food supplementation affected nestling phenotype only early in the breeding season in terms of elevated CORT_f levels and a tendency for more variable within‐brood CORT_f and FA. Early food supplemented nests therefore seemed to include at least some nestlings that faced increased stressors during development, possibly due to harsher environmental (e.g., related to food and temperature) conditions early in the breeding season that would increase sibling competition, especially in larger broods. The fact that CORT_f was positively, rather than inversely, related to nestling SMI further suggests that factors influencing CORT_f and SMI are likely operating over different periods or, alternatively, that nestlings in good nutritional condition also invest in high‐quality feathers.     

No need to shout: Effect of signal loudness on sibling communication in barn owls Tyto alba

In animal communication, signal loudness is often ignored and seldom measured. We used a playback experiment to examine the role of vocal loudness (i.e., sound pressure level) in sibling to sibling communication of nestling barn owls Tyto alba. In this species, siblings vocally negotiate among each other for priority access to parental food resources. Call rate and call duration play key roles in this vocal communication system, with the most vocal nestlings deterring their siblings from competing for access to the food item next delivered by parents. Here, we broadcast calls at different loudness levels and call rate to live nestlings. The loudness of playback calls did not affect owlets' investment in call rate, call duration or call loudness. The rate at which playback calls were broadcast affected owlets' call rate but did not influence their response in terms of loudness. This suggests that selection for producing loud signals may be weak in this species, as loud calls may attract predators. Moreover, given that owlets do not overlap their calls and that they communicate to nearby siblings in the silence of the night, loud signals may not be necessary to convey reliable information about food need.     

Is Mate Provisioning Predicted by Ornamentation? A Test with Northern Cardinals (Cardinalis cardinalis)

Male birds of many species feed their mates during courtship and incubation. The amount of food provided can be substantial and even essential for successful reproduction in some species, and can influence female nest attentiveness in many others. Additionally, mate provisioning may predict later nestling feeding rates. Females may thus benefit from being able to determine male provisioning effort. We assessed the expression of several ornaments, known to indicate condition in male northern cardinals (Cardinalis cardinalis), and compared these with mate provisioning rates, nestling feeding rates, and nest attentiveness. We found that male ornamentation may not be indicative of mate provisioning rates. Mate provisioning rate did not co‐vary with reproductive success, male feedings to nestlings, or nest attentiveness of females. However, females which were fed more often during incubation tended to provision nestlings less. Reduced female parental effort following extensive incubation feeding may be indicative of females using incubation feeding to assess future male parental effort. Male hormonal condition that favors high rates of nestling provisioning may be a proximate cause of mate provisioning during incubation, even in the absence of selection, favoring high rates of mate provisioning. Both sexes may have capitalized on this unselected behavior.     

Nestling aggression in broods of a siblicidal kingfisher, the laughing kookaburra

Third-hatched nestling in broods of the laughing kookaburra(Dacelo novaeguineae) are often killed by aggressive attacksfrom their older siblings within days of hatching. By installingsurveillance cameras inside nest hollows, we examined nestlingaggression over the "siblicidal" period, in particular to identifywhether parental behavior and competitive disparities betweennestlings affected aggression, and hence the likelihood ofsiblicide. Aggression decreased as nestlings aged and dominancehierarchies became established. The first-hatched nestling was the most aggressive. Fighting between the first-hatched nestlingand its closest rival (second-hatched nestling) increased whenthe hatch interval between them was short, when the size differencebetween them at hatching was small, and when the second nestlingwas female. Female nestlings are faster-growing than males,so young sisters may be an incipient threat requiring preemptiveaction by older siblings. When the second-hatched nestlingwas female, the first-hatched also attacked the third-hatched nestling more frequently. Thus the third-hatched nestling seemsto experience some of the "overflow" of aggression occurringbetween its two older siblings. Nestlings in siblicidal broodswere not fed less compared to nonsiblicidal broods; this isunsurprising because siblicide occurs when feeding rates arecomparatively low. However, siblicidal nestlings were broodedless, and in shorter bouts, which allowed them more time tofight.     

Increased sibling competition does not increase testosterone or corticosterone levels in nestlings of the spotless starling (Sturnus unicolor)

Nestling begging in passerine birds is a complex behaviour that is shaped by a multitude of ecological factors and could be physiologically mediated by varying levels of steroid hormones. Previous research has shown links between sibling competition and testosterone and corticosterone in several bird species. The spotless starling (Sturnus unicolor) is a medium sized passerine in which nestlings compete intensively for resources, often resulting in marked size hierarchies that can have profound effects on their fitness. We tested the hypothesis that an increase in sibling competition levels would result in increases in testosterone and corticosterone in this species. To this end we conducted a brood size manipulation, creating small, medium and large broods. This manipulation had the expected effect on morphology: nestling size and mass decreased with increasing brood size. Androgen levels varied in response to brood size manipulation but, contrary to expectations, the largest concentrations were found in reduced brood sizes. Corticosterone levels increased with increasing brood size, but this effect disappeared when we corrected for the time taken to process nestlings. Cell-mediated immune response was found to decrease with increasing brood size and testosterone levels. The results suggest that the proposed link between testosterone and corticosterone and sibling competition does not hold in this species, and underlines the diversity of species-specific responsiveness to steroids.     

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.