Sexual dimorphism,survival, and parental investment in relation to offspring sex in a precocial bird

Differential growth rate between males and females, owing to a sexual size dimorphism, has been proposed as a mechanism driving sex‐biased survival. How parents respond to this selection pressure through sex ratio manipulation and sex‐biased parental investment can have a dramatic influence on fitness. We determined how differential growth rates during early life resulting from sexual size dimorphism affected survival of young and how parents may respond in a precocial bird, the black brant Branta bernicla nigricans. We hypothesized that more rapidly growing male goslings would suffer greater mortality than females during brood rearing and that parents would respond to this by manipulating their primary sex ratio and parental investment. Male brant goslings suffered a 19.5% reduction in survival relative to female goslings and, based on simulation, we determined that a female biased population sex ratio at fledging was never overcome even though previous work demonstrated a slight male‐biased post‐fledging survival rate. Contrary to the Fisherian sex ratio adjustment hypothesis we found that individual adult female brant did not manipulate their primary sex ratio (50.39% male, n = 645), in response to the sex‐biased population level sex ratio. However, female condition at the start of the parental care period was a good predictor of their primary sex ratio. Finally, we examined how females changed their behavior in response to primary sex ratio of their broods. We hypothesized that parents would take male biased broods to areas with increased growth rates. Parents with male biased primary sex ratios took broods to areas with higher growth rates. These factors together suggest that sex‐biased growth rates during early life can dramatically affect population dynamics through sex‐biased survival and recruitment which in turn affects decisions parents make about sex allocation and sex‐biased parental investment in offspring to maximize fitness.     

Larger clutch size increases fledging success and offspring quality in a precocial species

1. We tested the hypothesis that the ability of parents to raise viable offspring limits clutch size in the greater snow goose ( Anser caerulescens atlanticus L.), a precocial bird.
2. We manipulated clutch size by exchanging complete clutches between pairs of nests to increase or decrease the clutch size by zero (control), one, two or three eggs in 314 nests over 2 years.
3. Pre-fledging survival of goslings increased in enlarged broods and decreased in reduced broods compared to control. Consequently, enlarged broods fledged more offspring and the reverse was true for reduced broods.
4. Size and mass of goslings near fledging was also higher in enlarged broods than in control, which suggests that offspring quality was also enhanced by the manipulation. This is contrary to the common trade-off between offspring numbers and quality.
5. Large families were dominant over smaller ones in feeding sites, which could explain the increased survival and growth of enlarged broods.
6. Our results suggest that the ability to raise young does not limit clutch size in this species and that parents could be more successful (i.e. increase both the number and quality of their offspring) by laying more eggs. However, the time required to lay additional eggs reduces the viability of all offspring and may explain why females do not lay more eggs.     

Why do goose parents adopt unrelated goslings? A review of hypotheses and empirical evidence,and new research questions

Adoption of unrelated offspring by successful breeders is one form of brood mixing and alloparental care that is widespread among geese and other waterfowl. Biparental care and long-lasting family bonds in geese are likely to affect the costs and benefits of adoption. Most hypotheses that have been proposed to explain this behaviour assume that the separation of the gosling from its original family is accidental, and that adoption forms the 'best of a bad job' solution. For the gosling, adoption is therefore thought to be the only, and thus adaptive, option. For parents, some hypotheses assume that there are costs of adoption (intergeneration conflict), while others assume that there are benefits (mutually beneficial). The few studies of adoption in wild goose populations indicate cost-neutrality or that there are small benefits to parents of adopting young. This agrees with studies of brood size, which suggest that large families provide benefits for goslings and parents alike. By contrast, most observed adoption attempts involve parental aggression against the lone gosling. However, incidental observations are likely to be biased towards adoptions that involve conspicuous behaviour, such as aggression, and might overlook inconspicuous adoptions. Studies of individually marked goslings are needed to identify the background of the adoption goslings in order to identify whether in geese, as in some larids and altricial species, adoption might be an active strategy of offspring to improve their fitness prospects. In addition, more experimental studies are needed to test predictions about the costs and benefits of large families in geese.     

Spatial structure and parental aggression in eider broods

The spatial position of young animals within a brood affects their survival, so that marginal individuals are at greater risk of predation. Spatial brood structuring may be caused by differences in offspring size, age, hunger, or active parental manipulation through aggression. Nepotistic manipulation of brood structure would confer fitness benefits for parents accepting nondescendant young. However, insufficient kin recognition has often been considered to preclude such nepotism in birds, particularly in precocial waterfowl. We explored the spatial structure of ducklings within broods of eiders, Somateria mollissima, a seaduck with frequent brood amalgamation. We compared the distribution of ducklings of different origin relative to reference females whose kinship to the ducklings was known. We also observed female aggression towards ducklings, to evaluate the role of parental manipulation of brood structure. We found a nonrandom distribution of ducklings within broods; a female's own young were on average closer to her than unrelated young were. We also found evidence for parental nepotism: whether the brood contained unrelated young was the strongest predictor of female aggression towards ducklings. The spatial position, hatch weight and relative size of ducklings showed no significant correlations with each other, suggesting that active parental manipulation may be needed to explain the observed spatial structure. Our study conflicts with previous anecdotal evidence suggesting that brood amalgamation in eiders results in the disintegration of parent-offspring bonds, preventing parental exploitation of nondescendant young. It also opens up the possibility that the spatial position of ducklings depends on their mother's status in the female dominance hierarchy. Copyright 2003 The Association for the Study of Animal Behaviour. Published by Elsevier Ltd. All rights reserved.      

Shared or Unshared Parental Care in Overwintering Brent Geese (Branta bernicla hrota)

We examine brood size effects on the behaviour of wintering parent and juvenile brent geese (Branta bernicla hrota) to test predictions of shared and unshared parental care models. The behaviour of both parents and offspring appear to be influenced by declining food availability over the winter. Parental vigilance increased with brood size and may be explained by vigilance having functions in addition to antipredator behaviour where the benefits are shared among the brood. There was no increase in parental aggression with brood size and this does not fit the prediction of shared care. Nevertheless, large families are able to monopolize better feeding areas compared with smaller families and large families static feed more but walk feed less than do small families, the former apparently being the preferred mode. The presence of additional young, rather than increasing the amount of parental aggression, seems to enhance the family's competitive ability. Because parents with large broods benefit from enhanced access to resources there is likely to be no additional significant cost in the parental care of larger broods (sensu Trivers 1972 ).     

Does Climate or Habitat Affect the Frequency of Cooperative Brood Rearing in Canada Geese?

Canada geese ( Branta canadensis ) are unusual because individuals use either of two different brood-rearing behaviors: cooperative broods (two or more merged broods attended by more than three parents) or two-parent families. We tested whether cooperative broods form in response to habitat or climatic conditions by examining variation in cooperative brood frequencies among Canada geese nesting in Connecticut from 1982 to 1996. Percent of goslings raised in cooperative broods ranged from 0 to 100% at a given site in different years, but the pattern of annual variation was different at each site. The sites were in close proximity to each other and had similar climates; thus, the differences in annual variation among sites was not likely to be a response to climatic conditions. Cooperative brood frequencies also varied among sites in each individual year, but sites with the most gang brooding in one year often had the least the next. Such would not be expected if gang brooding occurred in response to non-ephemeral habitat characteristics. Sites where gang brooding occurred and where it did not have similar food resources and predation risks. These findings failed to support the hypotheses that gang broods form in response to food competition or predation. Sites where gang broods occurred had more parent geese and more goslings than sites where they did not occur. Furthermore, the proportion of goslings raised in gang broods was correlated with the number of goslings and parents at the site. Our results support the hypothesis that gang broods form from the inadvertent mixing of goslings. This single factor, however, was not sufficient to account for all of the observed variation in gang brooding frequencies.     

Energy expenditure, nestling age, and brood size: an experimental study of parental behavior in the great tit Parus major

A brood manipulation experiment on great tits Parus major was performedto study the effects of nestling age and brood size on parentalcare and offspring survival. Daily energy expenditure (DEE)of females feeding nestlings of 6 and 12 days of age was measuredusing the doubly-labeled water technique. Females adjusted theirbrooding behavior to the age of the young. The data are consistentwith the idea that brooding behavior was determined primarilyby the thermoregulatory requirements of the brood. Female DEEdid not differ with nestling age; when differences in body masswere controlled for, it was lower during the brooding periodthan later. In enlarged broods, both parents showed significantlyhigher rates of food provisioning to the brood. Female DEE wasaffected by brood size manipulation, and it did not level offwith brood size. There was no significant effect of nestlingage on the relation between DEE and manipulation. Birds wereable to raise a larger brood than the natural brood size, althoughlarger broods suffered from increased nestling mortality ratesduring the peak demand period of the nestlings. Offspring conditionat fledging was negatively affected by brood size manipulation,but recruitment rate per brood was positively related to broodsize, suggesting that the optimal brood size exceeds the naturalbrood size in this population.     

Brood size and the economy of brood defence: examining Lack's hypothesis in a biparental cichlid fish

Synopsis We tested the explanatory value of two hypotheses reviewed by Lack (1954) in the maintenance of brood size in free-ranging convict cichlidsCichlasoma nigrofasciatum: (1) physiological constraints on egg production, and (2) behavioural constraints imposed by brood defence. Number of free-swimming young in 13 experimental (E) broods was augmented to the upper limit of the size distribution of natural broods (150 young); 18 control (C) broods were handled in the same way but brood size was not changed (mean ± SE = 69.5 ± 11.0). E and C brood sizes were measured at 5 day intervals. At day 20 (just before independence from parental care), 50.3 ± 9.4 (n = 9) young remained in E broods and 30.8 ± 7.8 (n = 8) young remained in C broods (p> 0.05). Offspring number did not differ significantly (p> 0.05) between C and E broods after day 10. Mean growth rate of offspring was significantly lower in E broods than in C broods, perhaps in response to increased density of young in the former. Both the convergence of offspring number in E and C broods and suppression of growth in E broods support a behavioural constraint; that during the first 10 days in which the young are free swimming, two parents are unable to defend large broods as successfully as small broods. A trade-off exists in parental investment between current and future reproduction. Extra-parental investment in current reproduction (eggs) does not result in an increased number of young at independence, therefore a behavioural constraint during brood defence should stabilize the evolution of clutch size.     

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.     

Survival of Dusky Canada Goose Goslings in Relation to Weather and Annual Nest Success

Abstract The dusky Canada goose (Branta canadensis occidentalis) population has been in long-term decline, likely due to reduced breeding productivity, but gosling survival of this population had not been examined. We studied gosling survival in broods of radiomarked adult females on the western Copper River Delta, Alaska, USA, during 1997–1999 and 2001–2003. Survival estimates for dusky Canada goose goslings to 45 days (x̄ = 0.32) were below estimates from most previous studies of geese. Daily survival of goslings increased with age and decreased with date of hatch. Precipitation during the first 3 days post-hatch was negatively related to gosling survival and this effect increased with date. Annual estimates of gosling survival were positively correlated with annual estimates of nest success, suggesting overlap in factors affecting nest and gosling survival. Nest success probably also directly affected gosling survival, because survival decreased with hatch date and more broods hatched from renests during years with low nest success. Gosling survival appears to play an important role in limiting current productivity of this population. Management directed at increasing nest success would likely also improve gosling survival. We recommend additional research directed at examining sources of gosling mortality and the link between nest success and gosling survival.     

Brood amalgamation in the Bristle-thighed Curlew Numenius tahitiensis: process and function

Alloparental care in birds generally involves nonbreeding adults that help at nests or breeding adults that help raise young in communal nests. A less often reported form involves the amalgamation of broods, where one or more adults care for young that are not their own. We observed this phenomenon among Bristle-thighed Curlew Numenius tahitiensis broods in western Alaska during 1990–1992. Amalgamation of broods generally involved the formation of temporary and extended associations. Temporary associations were formed by the incidental convergence of broods soon after they left their nests. During this period, parents defended distinct brood-rearing areas, were antagonistic to conspecifics and remained together for less than 3 days. Extended associations formed when chicks were 1–2 weeks old. Here, parents and their broods occupied distinct, but adjacent, brood-rearing areas and moved around as a unit. Whether a brood participated in either temporary or extended associations or remained solitary appeared to depend on brood density in the immediate area and on hatching date. When chicks were 3–4 weeks old, aggregations of up to ten broods formed wherein young mixed and parents defended a common brood-rearing area. All broods (n = 48) that survived to fledging joined such aggregations. Alloparental care involved only antipredator defence and was not associated with activities such as feeding and brooding. Most female parents abandoned their broods shortly after the young could fly and when aggregations were forming. The female parent of a pair always deserted its young before or on the same day as the male parent and, in every aggregation, one or two males continued to tend young for about 5 days longer than other male parents. In most cases, adults deserted the young 2–6 days before the young departed the area when about 38 days old. Bristle-thighed Curlews also formed temporary associations with American and Pacific Golden Plover Pluvialis dominica and Pluvialis fulva, Whimbrel Numenius phaeopus, Bar-tailed Godwit Limosa lapponica, Western Sandpiper Cal-idris mauri and Long-tailed Skua Stercorarius longicaudus. Curlews and other larger bodied species commonly attack-mobbed predators together, whereas smaller bodied species generally gave alarm calls and circled the predators. For all species, the intensity of antipredator defence by attending adults gradually decreased as young became older and aggregations formed. We suggest that amalgamation of broods among Bristle-thighed Curlew enhances predator defence, aids in the process of flock formation for migrating young, and allows females and some males to desert their young earlier.     

Facultative Adjustment of Brood Sex Ratio in Response to Indirect Manipulation of Behaviour

Sex allocation theory states that parents should adjust their offspring sex ratio according to the expected fitness returns from sons and daughters. Several recent studies indicate that such adaptive manipulation of offspring sex ratio is achievable, and that it may be influenced by e.g. morphological characters. Here we manipulate behaviour through interspecific cross-fostering of great tits ( Parus major ) and blue tits ( Cyanistes caeruleus ), and investigate its effect on the offspring sex ratio of adults that were themselves cross-fostered as chicks. The experience of being raised by a different species has previously been shown to result in aberrant species assortative behaviour and song, and a lowered dominance status during winter. Brood sex ratios of conspecifically breeding pairs with and without cross-fostered members were compared. Broods with at least one cross-fostered parent contained significantly more males than did control broods. Sex of cross-fostered parents did not influence the brood sex ratio. We conclude that female great tits and blue tits seem to be able to adjust the sex ratio of their broods, and that changes in their own or their partners' behaviour may elicit such adjustments.     

Ecological constraints on breeding system evolution: the influence of habitat on brood desertion in Kentish plover

1. One of the fundamental insights of behavioural ecology is that resources influence breeding systems. For instance, when food resources are plenty, one parent is able to care for the young on its own, so that the other parent can desert and became polygamous. We investigated this hypothesis in the context of classical polyandry when females may have several mates within a single breeding season, and parental duties are carried out largely by the male. 2. We studied a precocial wader, the Kentish plover Charadrius alexandrinus, that exhibits variable brood care such that the chicks may be raised by both parents, only by the female or, more often, only by the male. The timing of female desertion varies: some females desert their brood at hatching of the eggs and lay a clutch for a new mate, whereas other females stay with their brood until the chicks fledge. Kentish plovers are excellent organisms with which to study breeding system evolution, as some of their close relatives exhibit classical polyandry (Eurasian dotterel Eudromias morinellus, mountain plover Charadrius montanus), whereas others are polygynous (northern lapwing Vanellus vanellus). 3. Kentish plovers raised their broods in two habitats in our study site in southern Turkey: saltmarsh and lakeshore. Food intake was higher on the lakeshore than in the saltmarsh as judged from feeding behaviour of chicks and adults. As the season proceeded and the saltmarsh dried out, the broods moved toward the lakeshore. 4. As the density of plovers increased on lakeshore, the parents spent more time defending their young, and female parents stayed with their brood longer on the lakeshore. 5. We conclude that the influence of food abundance on breeding systems is more complex than currently anticipated. Abundant food resources appear to have profound implications on spatial distribution of broods, and the social interactions between broods constrain female desertion and polyandry.     

Environmental- and parental condition-related variation in sex ratio of kestrel broods

Variation of brood sex ratio was studied in a Finnish population of Eurasian Kestrels Falco tinnunculus breeding in an unpredictably variable environment. From those young that survived until 2–4 weeks of age, blood was collected and their sex determined from polymorphic DNA profiles produced by hybridisation with a human minisatellite probe. The sex ratio was male-biased during a year of food (vole) scarcity. Furthermore, in broods without mortality, contrasting seasonal trends in sex ratios emerged. In this subsample, the proportion of males increased with later laying date during years of low and moderate food supply, whereas the opposite was true in a year of relatively high food supply. These trends may indicate circumstances that favour the raising of different sex. The proportion of males in the brood was negatively correlated with body condition of both male and female parents, also reflecting an adaptive condition-dependent sex-ratio adjustment, or alternatively the inability of the parents to meet the requirements of the more energetically expensive female offspring. We discuss the limitations that unpredictable conditions during brood raising can impose on adaptive sex-ratio manipulation, particularly in species with sexual size dimorphism and consequent differences in the cost of raising the two sexes.     

Biparental care: short-term manipulation of partner contribution and brood size in the starling, Sturnus vulgaris

In species with biparental care, the evolutionarily stable investmentstrategy depends, among other factors, on the reproductive valueof the brood and on the contribution of one's partner. A shortfallin work rate by one parent should be partially compensated forby its partner, while both parents should invest more effortwhen there are more young. We simultaneously tested these predictionsby attaching weights to one member of pairs of European starlings(Sturnus vulgaris), thus reducing one partner's nest visitationrate, and by daily manipulation of brood sizes (between threeand seven chicks). Both sexes compensated to an equivalent degreefor their partner's lower work rate, while at the same timeadjusting flexibly to the daily brood size changes by increasingvisit rates to larger broods. However, this ability to compensatewas limited in the larger brood sizes, perhaps due to an upperlimit on provisioning rate. Weighted birds and their partnersshowed differences in prey types delivered, relative to controls,taking a lower proportion of leatherjackets. With regard tothe proximate cues affecting parental provisioning rate, beggingnoise levels (automatically recorded by computer from microphonesin the nest-box) increased with brood size, but average lengthof begging bout did not. As expected, visit rates per chickdecreased as brood size increased, and this was reflected inlower weight gains per day by chicks in larger broods. Theseresults agree in general with games theory models but revealimportant departures from our previous work with respect to(1) parents reaching an apparent ceiling to nest visitationrate at high brood sizes and (2) the ability to track thesebrood demands with short-term adjustments.     

Strong evidence for selection for larger brood size in a great tit population

We measured the selection pressure on brood size in a recentlyestablished population of great tits (Parus major L.) in thenorthern Netherlands by manipulating brood size in three years(1995: n = 51, 1997: n = 66, 1998: n = 51), and we estimatedfitness consequences in terms of local survival of both offspringand parents. Enlarged broods had highest fitness; the offspringfitness component was positively affected by manipulation andthe parental fitness component was unaffected. Parental survivaland the probability that parents produced a second clutch werenot affected by the treatment. However, parents that had raisedenlarged broods produced their second clutch later in the season.Clutch size, brood size, and laying date of birds recapturedin the next breeding season were largely independent of thetreatment. We conclude that there is strong evidence for selectionfor larger brood size and reject the individual optimizationhypothesis for this population because the number of young inthe nest predicts fitness independently of the manipulationhistory.     

Do maternal food deprivation and offspring predator cues interactively affect maternal effort in fish?

The state of the environment parents are exposed to during reproduction can either facilitate or impair their ability to take care of their young. Thus, the environmental conditions experienced by parents can have a transgenerational impact on offspring phenotype and survival. Parental energetic needs and the variance in offspring predation risk have both been recognized as important factors influencing the quality and amount of parental care, but surprisingly, they are rarely manipulated simultaneously to investigate how parents adjust care to these potentially conflicting demands. In the maternally mouthbrooding cichlid Simochromis pleurospilus, we manipulated female body condition before spawning and exposure to offspring predator cues during brood care in a two‐by‐two factorial experiment. Subsequently, we measured the duration of brood care and the number and size of the released young. Furthermore, we stimulated females to take up their young by staged predator attacks and recorded the time before the young were released again. We found that food‐deprived females produced smaller young and engaged less in brood care behaviour than well‐nourished females. Final brood size and, related to this, female protective behaviour were interactively determined by nutritional state and predator exposure: well‐nourished females without a predator encounter had smaller broods than all other females and at the same time were least likely to take up their young after a simulated predator attack. We discuss several mechanisms by which predator exposure and maternal nutrition might have influenced brood and offspring size. Our results highlight the importance to investigate the selective forces on parents and offspring in combination, if we aim to understand reproductive strategies.     

Age-dependent reproductive costs and the role of breeding skills in the Collared flycatcher

This study addressed whether there are any age‐related differences in reproductive costs. Of especial interest was whether young individuals increased their reproductive effort, and thereby their reproductive cost, as much as older birds when brood size was enlarged. To address these questions, a brood‐size manipulation experiment with reciprocal cross‐fostering of nestlings of young and middle‐aged female Collared flycatchers, Ficedula albicollis, was performed on the Swedish island of Gotland. Nestlings’ body mass, tarsus length and survival were recorded to estimate the parental ability and parental effort of the experimental female birds. Female survival and clutch size were recorded in the following years to estimate reproductive costs. We found that middle‐aged female flycatchers coped better with enlarged broods than younger females or invested more in reproduction. In the following year, young female birds that had raised enlarged broods laid smaller clutches than the females from all the other experimental groups. This result shows that the young female birds pay higher reproductive costs than the middle‐aged females. Both young and middle‐aged female flycatchers seemed to increase their reproductive effort when brood size was increased. However, such an increase resulted in higher reproductive costs for the young females. The difference in reproductive costs between birds of different ages is most likely a result of insufficient breeding skills of the young individuals.     

Growth of Greater White-Fronted Goose Goslings Relates to Population Dynamics at Multiple Scales

The abundance of greater white-fronted geese (Anser albifrons frontalis) on the Arctic Coastal Plain (ACP) of northern Alaska, USA, has more than tripled since the late 1990s; however, recent rate of annual population growth has declined as population size increased, which may indicate white-fronted geese on the ACP are approaching carrying capacity. We examined rates of gosling growth in greater white-fronted geese at 3 sites on the ACP during 2012–2014 to assist with predictions of future population trends and assess evidence for density-dependent constraints on recruitment. We marked goslings at hatch with individually coded webtags and conducted brood drives during early August to capture, measure, and weigh goslings. Annual estimates of gosling mass at 32 days old (range = 1,190–1,685) indicate that goslings had obtained >60% of asymptotic size. This rate of growth corresponds with that of other goose species and populations with access to high-quality forage and no limitations on forage availability, and is consistent with the overall increase in abundance of white-fronted geese at the ACP scale. Contrary to most previous investigations, age-adjusted mass of goslings did not decline with hatch date. Goslings grew faster in coastal areas than at inland freshwater sites. Taken together, these findings suggest forage was not limiting gosling growth rates in either ecosystem, but forage was of greater quality in coastal areas where goose foraging habitat is expanding because of permafrost subsidence. Spatial patterns of gosling growth corresponded with local-scale patterns of population density and population change; the areas with greatest rates of gosling growth were those with the greatest population density and rates of population increase. We found little evidence to suggest forage during brood rearing was limiting population increase of white-fronted geese on the ACP. Factors responsible for the apparent slowing of ACP-wide population growth are likely those that occur in stages of the annual cycle outside of the breeding grounds. Published 2021. This article is a U.S. Government work and is in the public domain in the USA.     

Azure‐winged Magpies Cyanopica cyanus trade off reproductive success and parental care by establishing a size hierarchy among nestlings

It is common in birds that the sizes of nestlings vary greatly when multiple young are produced in one nest. However, the methods used by parents to establish size hierarchy among nestlings and their effect on parental provisioning pattern may differ between species. In the Azure‐winged Magpie Cyanopica cyanus, we explored how and why parents controlled the sizes of nestlings. Asynchronous hatching was the main cause of size hierarchy within the brood, although the laying of larger eggs later in the laying sequence reduced this effect. Parents with asynchronous broods produced more eggs and fledged more nestlings than those with synchronous broods but their brood provisioning rates, food delivery per feeding bout and feeding efficiency did not differ. We performed a cross‐fostering experiment to synchronize some asynchronous broods. Provisioning rates of asynchronous broods were lower than those of synchronized broods, but the daily growth rates and fledging body mass of their nestlings were not different. Our findings indicate that parents of asynchronous broods can achieve higher reproductive success than those of synchronous broods based on the same parental care, and the same reproductive success as those of synchronized broods based on less parental care. It appears that parent birds can better trade off reproductive success and parental care by establishing a size hierarchy among nestlings.