Allocation of Male Parental Care in Relation to Paternity Within and Among Broods of the Common Yellowthroat (Geothlypis trichas)

The relationship between male parental care and paternity has been investigated in a number of avian species, but in many cases the influences of confounding factors, such as variation in male and territory quality, were not addressed. These sources of variation can be controlled for by making within-male comparisons between successive broods or within-brood comparisons between groups of fledglings in a divided brood. We studied the relationship between male parental care and paternity in the common yellowthroat ( Geothlypis trichas ) at three levels: between groups of fledglings in divided broods, between first and second broods of the same pair, and among all broods in the population. In this study we proposed three hypotheses: first, males in double-brooded pairs should provide relatively more parental care to broods in which they have higher paternity; secondly, after fledging and brood division, males should provide more care to related offspring; and finally, among all broods in the population, paternity should be related positively to male parental care. Brood division occurred in many of the broods studied; however, broods were not divided according to fledgling size or paternity. Furthermore, within divided broods, males fed within-pair and extra-pair fledglings at similar rates. For sequential broods of the same pair, male feeding rates were not associated with differences in paternity between broods. Among all broods in the population, males did not provide relatively less care to broods containing unrelated young. The lack of a relationship between male parental care and paternity suggests that either males cannot assess their paternity or the costs of reducing male parental care outweigh the benefits.     

Brood division in robins

Broods of fledgling robins Erithacus rubecula are sometimes divided between their parents so that each parent feeds only some of the chicks. These associations between a parent and certain of its young (‘family units’) are shown to be stable over periods of days. Brood division is most frequent in broods that are not followed by another nesting attempt. Experimental manipulation of the food supply suggests that brood division is relaxed when food is readily available. An analysis of the interactions between parents and chicks demonstrates that both adults and fledglings play a role in brood division. The possible functions of brood division are discussed with reference to ‘other types of care’, ‘parental efficiency’, ‘cheat countermeasure’ and ‘two types of chick’ hypotheses. Male parents feed chicks with shorter winglengths than do females: since females tend to have shorter winglengths than males, this suggests that chicks are cared for by parents of the opposite sex. Possible causes and consequences of this observation are discussed.     

Buffered development: resilience after aggressive subordination in infancy

Do aggressive dominance and subordination in vertebrate broods and litters affect development? We examined 1,167 fledglings from two-chick broods of the blue-footed booby (Sula nebouxii), a species in which the first-hatched chick dominates with violent attacks throughout the nestling period and subordinates suffer lower fledging success, but if both broodmates survive, they grow to the same size. There was little evidence that dominant fledglings were more likely to recruit into the breeding population than were subordinate fledglings, and there was no evidence that dominant and subordinate recruits differed in their age, date, brood size, or nest success at first reproduction or in their summed brood sizes or total nest success over the first 5 yr or first 10 yr of life. Compared with dominants, subordinate fledglings were less prejudiced by late hatching and established clutches earlier over the first 10 yr, and subordinate recruits had 33% larger broods over the first 5 yr. However, in broods where both chicks fledged, accumulated reproductive success for chicks up to age 5 yr was similar for dominants and subordinates. Exercising dominance throughout infancy apparently does not fortify a chick for the future and may incur a long-term cost, and suffering violent subordination throughout infancy has little or no prejudicial effect and may even steel a chick for adult life.     

Brood provisioning rates and fledgling behavior of Cordilleran Flycatchers in southwestern Colorado

The behavior of young songbirds after fledging is one of the least understood phases of the breeding cycle, although parental provisioning rates and movement of fledglings are key to understanding life history evolution. We studied Cordilleran Flycatchers (Empidonax occidentalis) at two sites in southwestern Colorado, USA, from 2012 to 2017. We banded and sexed breeding adults to determine the relative contributions of males and females to nestling and fledgling care, and attached radio‐transmitters to nestlings to facilitate observations of brood behavior after fledging. Females made 60% and 78% of total observed feedings of nestlings and fledglings, respectively. Parental provisioning rates increased with nestling age, and per‐nestling provisioning rates increased with brood size. Parental provisioning rates declined just before fledging, then increased just after fledging. Fledging times of individuals in broods were asynchronous and concentrated during the late afternoon and early evening. Males stopped caring for fledglings before females even though this species is single‐brooded, with some late‐season broods being abandoned by males. Broods spent the first three weeks after fledging within 400 m of nests, after which they began to disperse. Most aspects of the breeding biology of Cordilleran Flycatchers in our study, including the duration of nestling and fledging periods, female‐dominated provisioning, and movement patterns of fledglings, were similar to those of other Empidonax species. However, the times when young fledged were not concentrated in the morning as reported in most other songbirds, and this result warrants additional study of the timing of fledging in ecologically and taxonomically similar species. The increased per‐nestling provisioning rate with increasing brood size was unexpected, and additional study is needed to determine if this increase results from a trade‐off between adult annual survival and productivity favoring increased provisioning of young in larger broods, or from the existence of high‐quality individuals where larger clutches and higher provisioning rates are linked.     

Cooperation, conflict, and crèching behavior in goldeneye ducks

Crèching behavior, or brood amalgamation, results in offspring being reared by adults other than their genetic parents. Although a variety of hypotheses have been proposed to explain this behavior, most assume either that brood amalgamation is accidental (i.e., nonselected) or that adoption of young is selected for because of social benefits to the young and/or adopting parents. We propose, instead, that brood amalgamation is a function of two separate processes: brood desertion and brood adoption. To examine brood desertion, we develop a graphic model to predict when parents should abandon their young and we test this model experimentally for the Barrow's goldeneye (Bucephala islandica). As predicted, females deserted their offspring when the size of the brood was experimentally reduced. Brood adoption occurred when deserted ducklings joined other broods. However, the success of ducklings in doing so was strongly dependent on the availability of potential host broods and on the age of the recipient broods. Foreign ducklings were readily accepted into young broods (<10 d old) but invariably were rejected from old broods. We could detect no benefits or costs of brood adoption to the host females, contrary to the expectations of a social benefit hypothesis. Our experiments indicate that Crèching behavior is driven by selection on adults to abandon their brood when the benefits of continued investment are outweighed by the reduction in future reproduction and selection on deserted ducklings to join other broods to obtain parental care. Rather than a form of cooperative brood care, Crèching in goldeneyes is perhaps best considered as a form of reproductive parasitism, entailing parent-offspring conflict over brood desertion and intergenerational conflict over adoption of abandoned young.     

To call or not to call: parents assess the vulnerability of their young before warning them about predators

Communication about predators can reveal the effects of both conspecific and heterospecific audiences on signalling strategy, providing insight into signal function and animal cognition. In species that alarm call to their young, parents face a fundamental dilemma: calling can silence noisy offspring and so make them less likely to be overheard, but can also alert predators that young are nearby. Parents could resolve this dilemma by being sensitive to the current vulnerability of offspring, and calling only when young are most at risk. Testing whether offspring vulnerability affects parental strategy has proved difficult, however, because more vulnerable broods are often also more valuable. We tested experimentally whether parent white-browed scrubwren, Sericornis frontalis, assessed brood noisiness when alarm calling near nests. When a model predator was nearby, parents gave more alarm calls when playbacks simulated noisy broods, yet brood noisiness did not affect adult calling when only a control model was present. Parents were therefore sensitive to the tradeoff between silencing young and alerting predators to the presence of nests. Our study demonstrates that receiver vulnerability can affect signalling decisions in species other than primates.     

Costs and benefits of parental care in eastern kingbirds

We manipulated brood sizes of eastern kingbirds (Tyrannus tyrannus)to measure the costs and benefits of parental care and to testwhether kingbirds showed evidence of individual optimizationof reproductive effort. We found that the number of feedingtrips (trips/h) increased and that per capita feeding rates(trips/nestling/h) declined as brood size increased. The declinein per capita feeding rates was mostly due to high feeding rateto broods of one: parents made roughly equal number of tripsto feed each nestling in broods of two to five. Nonetheless,nestling mass declined with brood size, probably because largebroods were fed more small prey. Nestling condition (mass adjustedfor structural size) differed only between broods of one andfive. After controlling for effects of brood size, feeding rateshad no supplementary influence on either nestling size or condition,but productivity and feeding rate were positively and significantlyrelated. Adult male condition did not vary with brood size,manipulated brood size, or total feeding rate, but declinedas the pair's per capita feeding rates increased. In addition,males that returned to breed were in better condition beforeleaving for migration than those that failed to return. Femalecondition tended to decline, and the probability of returningto breed dropped when broods were enlarged. However, femalecondition was independent of the probability of returning. Ourresults show that high feeding rates were costly, but that theycarried benefits (greater productivity). Some evidence for individualoptimization of reproductive effort existed: variability innestling and adult female condition were better explained bychanges in brood size than by the actual number of young inthe nest. However, most evidence supported the alternative thatincreased brood size was equally costly for all birds     

Brood division and transition to independence in Blackbirds Turdus merula

Blackbirds Turdus merula rearing young in the Botanic Garden, Oxford, were observed over three summers (1979–81). Between 0 and 10 days after fledging the young were divided between the parents so that each fed only certain fledglings and refused to feed others. This division was temporally stable. In broods where another nesting attempt followed, the male usually took responsibility for all the young, but in final broods they were divided fairly evenly. The probability of a fledgling surviving to independence declined as the number of young a parent fed increased; thus division should be favoured. However, if the female fed some young the inter-nest interval increased and the potential number of young that could be raised in that season was curtailed. This trade-off is examined by means of a model. After fledging the young improved in their ability to capture prey successfully and increased the size of the prey taken. At 15–24 days after fledging, self-feeding became more profitable than parental feeding and the young became fully independent. The timing of this transition is influenced by the parents, and it is suggested that by dividing the brood, parental feeding can be more carefully regulated so that finer control over the timing of independence is achieved.     

Parental physiological condition and reproductive success in chinstrap penguins (Pygoscelis antarctica)

Recent studies suggest that parental resource allocation may be the most important factor explaining differences in reproductive output among parents. That said at least two different hypotheses of balance between parental foraging effort and resource allocation have been proposed. First, parents with high foraging effort have high reproductive success. Second, parents with higher allocation of resources to offspring have high reproductive success. We tested the second hypothesis using chinstrap penguins (Pygoscelis antarctica) as a model. We evaluated nutritional condition of the parents using blood urea, uric acid, creatine kinase, and cholesterol levels. We evaluated reproductive success according to total mass of the brood and asymmetries inside the brood. We measured the degree of asymmetry using weight and culmen length. Generalized linear models were used to examine relationships between adult plasma urea levels with year, nest position, and degree of asymmetry in chicks. Our results demonstrate that lighter broods were more asymmetric and associated with lower values of adult plasma urea, uric acid, and creatine kinase. We interpret these findings as evidence that the birds allocate fewer resources to their chicks than adults with more symmetric broods are.     

Post-fledging brood and care division in the roseate tern (Sterna dougallii)

Extended post-fledging parental care is an important aspect of parental care in birds, although little studied due to logistic difficulties. Commonly, the brood is split physically (brood division) and/or preferential care is given to a subset of the brood by one parent or the other (care division). Among gulls and tern (Laridae), males and females generally share parental activities during the pre-fledging period, but the allocation of parental care after fledging is little documented. This study examined the behaviour of male and female roseate terns (Sterna dougallii) during the late chick-rearing and early post-fledging periods, and in particular the amount of feeds and the time spent in attendance given to individual chicks/fledglings. Pre-fledging parental care was biparental in all cases. Post-fledging parental care was dependent on the number of fledglings in the brood. Males and females continued biparental care in clutches with one surviving fledgling, while in two-fledgling clutches, males fed the A-fledgling while females fed the B-fledgling. Overall, there was no difference in attendance, only in feeds. This division of care may be influenced by the male only being certain of the paternity of the A-chick but not by chick sex.     

Not for Parents Only: Begging Calls Allow Nest‐Mate Discrimination in Juvenile Zebra Finches

The benefits of recognition of family members may range from inbreeding avoidance to cooperative and coordinated behaviors within the family group. In birds, recognition of family members has almost exclusively been studied between parents and offspring or within cooperatively breeding societies. Yet, recognition of nest‐mates could be of special importance in recently fledged birds of colonial species by helping in locating the nest, maintaining family group cohesion, or allowing detection of feeding opportunities by recognizing the begging calls nest‐mates produced on the return of a parent. Here we study nest‐mate discrimination based on begging calls in fledglings of domesticated zebra finches (Taeniopygia guttata), a gregarious songbird living in loose colonies in which juveniles may gather in crèches and are fed by parents up to 20 d after fledging. Using playback tests, we show that fledglings called more and spent more time near the loudspeaker in response to the begging calls of their nest‐mates than to the calls of other familiar individuals. Because each fledgling was exposed to the repeated association of the begging calls of its nest‐mates and the subsequent feeding of its parents, this preferential response to the nest‐mates' calls could be a conditioned response to the food reward. Whereas fledglings answered more to male fledgling calls than to female fledgling calls, response to playback was influenced neither by the sex of the subject nor by its brood size. Discriminant function analysis based on acoustic parameters showed that begging calls carried an individual signature as well as a brood signature which might account for such nest‐mate discrimination. Begging signals are major study systems of the evolution of communication in the face of conflicts of interest between signalers and receivers. Our results suggest that eavesdropping and communication networks may be other informative frameworks to understand the design of offspring solicitation signals.     

Brood parasitism increases provisioning rate, and reduces offspring recruitment and adult return rates, in a cowbird host

Interspecific brood parasitism in birds presents a special problem for the host because the parasitic offspring exploit their foster parents, causing them to invest more energy in their current reproductive effort. Nestling brown-headed cowbirds (Molothrus ater) are a burden to relatively small hosts and may reduce fledgling quality and adult survival. We documented food-provisioning rates of one small host, the prothonotary warbler (Protonotaria citrea), at broods that were similar in age (containing nestlings 8–9 days old), but that varied in composition (number of warbler and cowbird nestlings) and mass, and measured the effect of brood parasitism on offspring recruitment and adult returns in the host. The rate of food provisioning increased with brood mass, and males and females contributed equally to feeding nestlings. Controlling for brood mass, the provisioning rate was higher for nests with cowbirds than those without. Recruitment of warbler fledglings from unparasitized nests was 1.6 and 3.7 times higher than that of fledglings from nests containing one or two cowbirds, respectively. Returns of double-brooded adult male and female warblers decreased with an increase in the number of cowbirds raised, but the decrease was more pronounced in males. Reduced returns of warbler adults and recruitment of warbler fledglings with increased cowbird parasitism was likely a result of reduced survival. Cowbird parasitism increased the warblers’ investment in current reproductive effort, while exerting additional costs to current reproduction and residual reproductive value. Our study provides the strongest evidence to date for negative effects of cowbird parasitism on recruitment of host fledglings and survival of host adults.     

Competition with a host nestling for parental provisioning imposes recoverable costs on parasitic cuckoo chick's growth

Chicks of the brood parasitic common cuckoo (Cuculus canorus) typically monopolize host parental care by evicting all eggs and nestmates from the nest. To assess the benefits of parasitic eviction behaviour throughout the full nestling period, we generated mixed broods of one cuckoo and one great reed warbler (Acrocephalus arundinaceus) to study how hosts divide care between own and parasitic young. We also recorded parental provisioning behaviour at nests of singleton host nestlings or singleton cuckoo chicks. Host parents fed the three types of broods with similar-sized food items. The mass of the cuckoo chicks was significantly reduced in mixed broods relative to singleton cuckoos. Yet, after the host chick fledged from mixed broods, at about 10-12 days, cuckoo chicks in mixed broods grew faster and appeared to have compensated for the growth costs of prior cohabitation by fledging at similar weights and ages compared to singleton cuckoo chicks. These results are contrary to suggestions that chick competition in mixed broods of cuckoos and hosts causes an irrecoverable cost for the developing brood parasite. Flexibility in cuckoos' growth dynamics may provide a general benefit to ecological uncertainty regarding the realized successes, failures, and costs of nestmate eviction strategies of brood parasites.     

Recognition of Young in A Colonially Nesting Bird

Parents ought to restrict costly parental care to their genetic offspring and, particularly when the risk of misdirecting care is high, parent‐offspring recognition may evolve. I tested whether adult cave swallows, which nest in dense colonies and feed fledglings in mixed‐family groups, discriminate against unrelated young, using temporary chick transfers at two nestling ages and a cross‐fostering experiment. Temporary chick transfers indicated that parents bias feedings toward their own offspring near fledging (18 d) but not at about halfway through the nesting period (10 d). I also examined how parents learn to identify their offspring by cross‐fostering young 3 d after hatching and testing parental response 2 wks later. Adults did not favor their own offspring over unrelated nestlings when both were unfamiliar to the focal parents. However, when parents encountered two of their own offspring, one of which was reared by foster parents, they preferentially fed the familiar nestling. By recognizing young, cave swallow parents reduce some risks of misdirected parental investment (mobile fledglings) but not others (extra‐pair young and intraspecific brood parasitism).     

Sexual conflict among polygynous pied flycatchers feeding young

In the polygynous pied flycatcher, Ficedula hypoleuca, reproductivesuccess of females is constrained by male food provisioningduring the nestling period. Hence, there will be conflictinginterests among the male and each of his mates as to how malefeeding effort should be shared among broods. This paper describesthree experiments designed to examine the parental behaviorof the members of a bigynous trio, i.e., the male and his twomates, in light of these conflicts. In all experiments, primaryand secondary broods were manipulated to hatch on the same dayto reduce the difference in brood-reproductive value due toage. Males divided their effort equally when the two broodswere the same size. However, males did not allocate their investmentin proportion to brood size when brood sizes differed, but investedmore heavily per young in the larger broods. This finding suggeststhat males tried to optimize the joint effort of their two mates.Males and females showed similar responses to experimental reductionin brood demands, which indicates no difference in their willingnessto invest in offspring. When one of the male’s mates wasremoved temporarily, the male increased his total feeding rateand provided proportionately more food to the "motherless" brood.Through flexible allocation of parental investment, males seemable to optimize their reproductive interests in the two broods.The only way a polygynously mated female might successfullyincrease the amount of male assistance at her nest is to makeher own brood more valuable for the male, relative to the otherbroods he might have. We discuss some ways this might be achieved.[Behav Ecol 1991;2:106–115]     

Double brooding and polygyny in Sedge Warblers Acrocephalus schoenobaenus breeding in north-west England

Sedge Warbler breeding was studied at a site in Greater Manchester, UK, during 1991 and 1993. Birds were individually colour-ringed and, in the 2 years of the study, 18 pairs and 38 nesting attempts were observed. In both years, the majority of pairs (> 90%) attempted a second brood after successfully raising their first. Overall nest survival was 44% and the median reproductive output of individual males was 6.5 fledglings in each year (range 0–10 and 0–15 in 1991 and 1993, respectively). After fledging, one or both parents continued to feed the young for up to 15 days (median 11, range 0–15 days). One male was apparently bigamous in 1991 and in 1993, raising four broods successfully in 1993 and 25 fledglings over the 2 years. These observations suggest that double brooding is the normal strategy for Sedge Warblers in this population and that polygyny may be common, although easily overlooked.     

Optimal brood size and its limiting factors in the Rufous Turtle DoveStreptopelia orientalis

Optimal brood size and its limiting factors of the Rufous Turtle Dove,Streptopelia orientalis, were studied at the campus of the University of Tsukuba, Japan, during the breeding season in 1990–92. The dove usually lays two eggs in a nest. I made nests of a brood size of one and three by transferring a hatchling from one nest to the other, and compared their fledging success, factors of breeding failure, weight and tarsus length at fledging, growth rate and nestling period with those of a brood of two. The index of fitness (fledgling weight multiplied by average number of fledglings per nest) was almost the same in broods of two and three. However, the highest variation in fledging weight within the brood and the extension of nestling period were observed in broods of three, which caused the extension of inter-brood interval and consequently the smaller number of broods in the total breeding season. Therefore, broods of three would not have an advantage in producing more offspring than broods of two. Crop milk production had an effect on the growth of nestlings in the early phase of the nestling period, but the rapid growth in the granivorous phase compensated for the growth delay of the smallest nestling in broods of three. Small brood size and a large number of broods in a season would also be more effective under high predation pressure.     

Sex-specific transgenerational effects of early developmental conditions in a passerine

Most studies dealing with the trade-off between offspring number and quality have overlooked the long-term consequences for the progeny. High investment in offspring number usually results in an increased competition among nest mates. The deterioration of the early developmental conditions, due to this increased competition, can impair individual quality over the long term, and subsequently affect survival and lifetime fecundity. Moreover, the consequences of the allocation rule to offspring number vs. quality can extend across generations and give raise to grandparental effects. These transgenerational trade-offs have been explored rarely. In the present study, we manipulated the breeding effort of captive zebra finches ( Taeniopygia guttata ) by offering them enlarged or reduced broods. Offspring reared under these conditions were allowed to breed freely in an outdoor aviary, during their entire lifespan. Second-generation fledglings whose mother was raised in enlarged broods were in lower body condition than offspring whose mother was raised in reduced broods. However, second-generation fledglings were not affected by the brood size experienced by the father. These results show that the solution of parental dilemma, whether producing a small number of high quality offspring or a large number of poor quality descendants, must take into account the long-term transgenerational effects acting on grandchildren.  © 2007 The Linnean Society of London, Biological Journal of the Linnean Society , 2007, 91 , 469–474.     

Vocal begging by nestlings and vulnerability to nest predation in Meadow Pipits Anthus pratensis; to what extent do predation costs of begging exist?

Models of the evolution of parent-offspring communication and of brood size assume that the noisy begging by the young is costly in terms of predation. The present study was designed to investigate cause-and-effect relations between the behaviour of the offspring and adult Meadow Pipits Anthus pratensis and the risk of nest predation. Harriers ( Circus spp.), which can use auditory signals, were the main predators in the study area. I found that the intensity of vocal begging by broods did not influence their survival, despite the fact that the proportion of time that parents sacrificed to nest guarding declined with increased begging and some broods readily begged if a stimulus resembling the approaching parent was produced. The lack of fitness penalties for noisy broods was attributed to the following factors: (1) the open habitat was easy to scan, and parents silenced the young before feeding them if a predator was close (this adaptation was demonstrated in an experiment) and (2) parent birds could not deter harriers searching for prey, and therefore nest guarding did not influence the probability of nest detection. Pitfalls in the interpretation of relations between the vocal begging and the vulnerability to nest predation are discussed.