Facultative response to a kleptoparasite by the cooperatively breeding pied babbler

In many cases of interspecific kleptoparasitism, hosts developdefensive behaviors to minimize the impact of kleptoparasites.Because vigilance and defensive behaviors are often costly,selection should favor hosts that adjust the amount of investmentneeded to minimize losses to kleptoparasitism. However, examplesof such facultative responses are rare. Here, we investigatethe response of cooperatively breeding pied babblers (Turdoidesbicolor) to the drongo (Dicrurus adsimilis), an avian kleptoparasitethat regularly follows pied babbler groups, often giving alarmcalls to alert the group to predators but also occasionallygiving false alarm calls in order to steal food items. We showthat pied babbler response to drongos varies markedly accordingto babbler group size. In small groups, where there are fewindividuals available to act as sentinels, babblers sentinelless when a drongo is present and respond strongly to drongoalarm calls. However, in large groups, where there are manyindividuals available to participate in predator vigilance,babblers sentinel more often when a drongo is present, rarelyrespond to drongo alarm calls, and aggressively displace drongos,with a consequent decline in the number of successful kleptoparasitismevents. This behavior represent a facultative response to akleptoparasite according to the costs versus benefits of toleratingtheir presence.     

Variable fledging age according to group size: trade-offs in a cooperatively breeding bird

Group living can provide individuals with several benefits, including cooperative vigilance and lower predation rates. Individuals in larger groups may be less vulnerable to predation due to dilution effects, efficient detection or greater ability to repel predators. Individuals in smaller groups may consequently employ alternative behavioural tactics to compensate for their greater vulnerability to predators. Here, we describe how pied babbler (Turdoides bicolor) fledging age varies with group size and the associated risk of nestling predation. Nestling predation is highest in smaller groups, but there is no effect of group size on fledgling predation. Consequently, small groups fledge young earlier, thereby reducing the risk of predation. However, there is a cost to this behaviour as younger fledglings are less mobile than older fledglings: they move shorter distances and are less likely to successfully reach the communal roost tree. The optimal age to fledge young appears to depend on the trade-off between reduced nestling predation and increased fledgling mobility. We suggest that such trade-offs may be common in species where group size critically affects individual survival and reproductive success.     

Parental aggression against dependent young results in task partitioning in a cooperatively breeding bird

In cooperatively breeding species, helpers can alleviate reproductive constraints by assuming the role of primary carers to first-born young, liberating breeders to invest in subsequent broods. However, evidence on how first-born young are transferred to helpers is currently lacking. We propose that breeder-offspring aggression might facilitate inter-brood division and test this idea using data from a wild population of cooperatively breeding pied babblers (Turdoides bicolor). After second-brood young hatch, breeders become increasingly aggressive to first-brood fledglings and attack them when they beg for food. After an attack, fledglings reduce begging. Helpers are much less aggressive to begging fledglings and fledglings subsequently tend to target helpers, rather than breeders, when begging for food. In this way, first-born dependent young are transferred to helpers, resulting in a partitioning of tasks among breeders and helpers. Task partitioning in eusocial insects is thought to be determined by the morphological or physiological characteristics of individuals. This complementary study suggests that flexible behavioural strategies may also result in specialized roles in cooperatively breeding vertebrates.     

The benefits of pair bond tenure in the cooperatively breeding pied babbler (Turdoides bicolor)

The benefits of stable pair bonds (that persist between breeding attempts) have been well described, but are relatively less well known in cooperatively breeding species. If pair bonds are beneficial, then it is possible that the bond between the behaviorally and socially dominant pair may influence factors such as reproductive success and group stability in cooperative species. Here, we used long‐term data to investigate the relationships between pair bond tenure, reproductive success, and group stability in the cooperatively breeding pied babbler (Turdoides bicolor). Pair bond tenure positively influenced both the number of offspring recruited annually per pair and total reproductive success (over entire pair bond duration), indicating that pair bond tenure has an important influence on reproductive success. The likelihood of immigration into the group was lower for groups containing a bonded pair with long tenure, indicating that the duration of pair bonds may impact group stability. These findings suggest that pair tenure, a hitherto relatively unexplored factor in cooperative species, may have an important influence on group dynamics.     

Sex-biased preferential care in the cooperatively breeding Arabian babbler

In many social birds there are sex differences in dispersal patterns, with males commonly remaining in their natal group whereas females typically disperse at adolescence. Group members may therefore increase their fitness by preferentially caring for offspring of a particular sex according to social circumstances. Although previous studies have focussed on intragroup social factors that may affect preferential care, we propose that the relative size of neighbouring groups is of primary importance. Here we show that in the cooperatively breeding Arabian babbler (Turdoides squamiceps), parents preferentially feed male offspring when relative group size is small, and female offspring when group size is large. Unlike parents, helpers consistently favour young of the opposite sex to themselves, suggesting the risk of competition with members of the same sex for future breeding opportunities may override other considerations. These results emphasize the complexity of investment strategies in relation to social circumstances and the variable benefits of raising males vs. females in a species with sex-biased philopatry.     

Costly reproductive competition between females in a monogamous cooperatively breeding bird

In many cooperatively breeding societies, only a few socially dominant individuals in a group breed, reproductive skew is high, and reproductive conflict is common. Surprisingly, the effects of this conflict on dominant reproductive success in vertebrate societies have rarely been investigated, especially in high-skew societies. We examine how subordinate female competition for breeding opportunities affects the reproductive success of dominant females in a monogamous cooperatively breeding bird, the Southern pied babbler (Turdoides bicolor). In this species, successful subordinate reproduction is very rare, despite the fact that groups commonly contain sexually mature female subordinates that could mate with unrelated group males. However, we show that subordinate females compete with dominant females to breed, and do so far more often than expected, based on the infrequency of their success. Attempts by subordinates to obtain a share of breeding impose significant costs on dominant females: chicks fledge from fewer nests, more nests are abandoned before incubation begins, and more eggs are lost. Dominant females appear to attempt to reduce these costs by aggressively suppressing potentially competitive subordinate females. This empirical evidence provides rare insight into the nature of the conflicts between females and the resultant costs to reproductive success in cooperatively breeding societies.     

Reproductive success and helper effects in the cooperatively breeding grey-crowned babbler

Cooperative breeding, where some individuals help to raise offspring that are not their own, is a relatively rare social system in birds. We studied the breeding biology of a declining cooperative breeder, the grey-crowned babbler Pomatostomus temporalis , with the aim of isolating the social factors that affect its reproductive success. Most breeding pairs were assisted by philopatric offspring, although pairs could breed successfully without helpers. Females laid up to four clutches (usually three eggs per clutch) per season. Male (but not female) helpers increased the number of young fledged from individual nests and the likelihood of re-nesting, resulting in higher seasonal fledgling production. Helper effects on brood size and fledgling production were greater in the second year of the study, which was also characterized by higher nest failure. This suggests that helpers enhance reproduction more in poor conditions. Our study demonstrates the interacting effects of social and ecological factors on reproductive success, and that retention of offspring is not always beneficial for the breeders in cooperative species.     

Experimentally reduced male attractiveness increases parental care in the pied flycatcher Ficedula hypoleuca

This study reports effects of experimental manipulations ofreproductive effort and the size of the male's white foreheadpatch (a secondary sexual trait), on provisioning rates, reproductivesuccess, and parental breeding dispersal distance in the piedflycatcher, Ficedula hypoleuca. Parents caring for enlargedbroods resulting from manipulated clutches provisioned nestsat higher rates than parents with reduced broods. Males with a reduced forehead patch fed their nestlings more in relationto males with an unmanipulated forehead patch, and their youngfledging with a longer tarsi. This suggests that males witha reduced attractiveness may perceive their own attractivenessand they devote more time available for parental effort given their poorer prospects in male contest competition and/or femaleattraction for extra-pair copulations. However, their femalesdid not alter their provisioning effort and this runs counterto both the differential allocation and the partner-compensationhypotheses. An artificial decrease in a male secondary sexualtrait led to a wider breeding dispersal distance between successiveyears.     

Compensatory and additive helper effects in the cooperatively breeding Seychelles warbler (Acrocephalus sechellensis)

In cooperatively breeding species, care provided by helpers may affect the dominant breeders’ investment trade‐offs between current and future reproduction. By negatively compensating for such additional care, breeders can reduce costs of reproduction and improve their own chances of survival. Alternatively, helper care can be additive to that of dominants, increasing the fledging fitness of the current brood. However, the influence helpers have on brood care may be affected by group size and territory quality. Therefore, the impact of helping needs to be disentangled from other factors determining offspring investment before conclusive inferences about the effect of help on additive and compensatory care can be made. We used 20 years of provisioning data to investigate the effect of helping on provisioning rates in the facultative cooperatively breeding Seychelles warbler Acrocephalus sechellensis. Our extensive dataset allowed us to statistically disentangle the effects of helper presence, living in larger groups and different food availability. We show compensatory and additive care (i.e., partial compensation) in response to helper provisioning. Helpers lightened the provisioning load of the dominant male and female and increased total provisioning to nestlings. This was irrespective of group size or territory quality (food availability). Moreover, our results illustrate sex‐specific variation in parental care over the course of the breeding event. We discriminate between temporal variation, group size, and territory quality processes affecting cooperative care and as such, gain further insight into the importance of these factors to the evolutionary maintenance of helping behavior.     

Testing the predictions of sex allocation hypotheses in dimorphic,cooperatively breeding riflemen

Evolutionary theory predicts that parents should invest equally in the two sexes. If one sex is more costly, a production bias is predicted in favour of the other. Two well‐studied causes of differential costs are size dimorphism, in which the larger sex should be more costly, and sex‐biased helping in cooperative breeders, in which the more helpful sex should be less costly because future helping “repays” some of its parents’ investment. We studied a bird species in which both processes should favor production of males. Female riflemen Acanthisitta chloris are larger than males, and we documented greater provisioning effort in more female‐biased broods indicating they are likely costlier to raise. Riflemen are also cooperative breeders, and males provide more help than females. Contrary to expectations, we observed no male bias in brood sex ratios, which did not differ significantly from parity. We tested whether the lack of a population‐wide pattern was a result of facultative sex allocation by individual females, but this hypothesis was not supported either. Our results show an absence of adaptive patterns despite a clear directional hypothesis derived from theory. This appears to be associated with a suboptimal female‐biased investment ratio. We conclude that predictions of adaptive sex allocation may falter because of mechanistic constraint, unrecognized costs and benefits, or weak selection.     

Offspring sex ratios correlate with pair-male condition in a cooperatively breeding fairy-wren

We examined sex allocation patterns in island and mainland populationsof cooperatively breeding white-winged fairy-wrens. The markeddifferences in social structure between island and mainlandpopulations, in addition to dramatic plumage variation amongmales both within and between populations, provided a uniquesituation in which we could investigate different predictionsfrom sex allocation theory in a single species. First, we testthe repayment (local resource enhancement) hypothesis by askingwhether females biased offspring sex ratios in relation to theassistance they derived from helpers. Second, we test the malequality (attractiveness) hypothesis, which suggests that femalesmated to attractive high-quality males should bias offspringsex ratios in favor of males. Finally, we test the idea thatfemales in good condition should bias offspring sex ratios towardmales because they are able to allocate more resources to offspring,whereas females in poor condition should have increased benefitsfrom producing more female offspring (Trivers-Willard hypothesis).We used molecular sexing techniques to assess total offspringsex ratios of 86 breeding pairs over 2 years. Both offspringand first brood sex ratios were correlated with the pair-male'sbody condition such that females increased the proportion ofmales in their brood in relation to the body condition (masscorrected for body size) of their social partner. This relationwas both significant and remarkably similar in both years ofour study and in both island and mainland populations. Althoughconfidence of paternity can be low in this and other fairy-wrenspecies, we show how this finding might be consistent with themale quality (attractiveness) hypothesis with respect to malecondition. There was no support for the repayment hypothesis;the presence of helpers had no effect on offspring sex ratios.There was weak support for both the male quality (attractiveness)hypothesis with respect to plumage color and the maternal conditionhypothesis, but their influence on offspring sex ratios wasnegligible after controlling for the effects of pair-male condition.     

Prolonged offspring dependence and cooperative breeding in birds

It has been suggested that the evolution of cooperative breedingin birds is associated with unusually long periods of offspringdependence ; this appears paradoxical because cooperative breedersoften produce more broods than their noncooperatively breedingrelatives. I compared the duration of parental care betweencooperatively and noncooperatively breeding species using phylogeneticallyindependent contrasts and matched pairs. The incubation andnestling periods did not differ between the two parental caresystems, but the duration of postfledging offspring care wassignificantly longer in species that regularly breed cooperatively.This relationship remained when other factors that are thoughtto affect the duration of fledgling care (breeding habitat,body size, latitude of breeding, diet) were controlled statistically.Cooperative breeders appear to provide more prolonged postfledgingcare because additional care providers reduce the costs of parenting, offspring have less incentive to become independent,and a division of labor can develop during reproduction—helperscontinue to feed fledglings while breeders initiate the nextnesting attempt.     

Reproductive suppression in female cooperatively breeding cichlids

Suppression by dominants of female subordinate reproduction has been found in many vertebrate social groups, but has rarely been shown experimentally. Here experimental evidence is provided for reproductive suppression in the group-living Lake Tanganyika cichlid Neolamprologus pulcher. Within groups of three unrelated females, suppression was due to medium- and small-sized females laying less frequently compared with large females, and compared with medium females in control pairs. Clutch size and average egg mass of all females depended on body size, but not on rank. In a second step, a large female was removed from the group and a very small female was added to keep the group size constant. The medium females immediately seized the dominant breeding position in the group and started to reproduce as frequently as control pairs, whereas clutch size and egg mass did not change. These results show that female subordinate cichlids are reproductively capable, but apparently suppressed with respect to egg laying. Nevertheless, some reproduction is tolerated, possibly to ensure continued alloparental care by subordinate females.