Communal roosting,thermoregulatory benefits and breeding group size predictability in cooperatively breeding sociable weavers

Extreme temperatures impose energy costs on endotherms through thermoregulation and different adaptations help individuals to cope with these conditions. In social species, communal roosting and huddling are thought to decrease the energetic requirement of thermoregulation under low temperatures. This is likely to represent an important mechanism by which individuals save energy during the coldest parts of the year and hence to represent a non‐breeding benefit of sociality. Here, we investigate the potential thermoregulatory benefits of group living in roosting groups of sociable weavers Philetairus socius, a colonial cooperatively breeding passerine that builds communally a massive nest structure with several independent chambers wherein individuals breed and roost throughout the year. To investigate the benefits of sociality during the non‐breeding season, we studied the thermal environment during roosting in relation to group size. In addition, to understand the link between non‐breeding and breeding sociality in this species we studied group size stability between the pre‐breeding and breeding periods. As expected, we found that the nest chamber's night‐time temperature is strongly related to the number of birds roosting together, especially during cold nights. Specifically, birds in larger groups spent less time below the critical thermal minimum temperature (i.e. the temperature below which energy expenditure increases substantially). They were less exposed to external temperature variations. We also found a positive relationship between the number of birds roosting during winter and the breeding group size, indicating breeding group size predictability. In cooperative breeders such as the sociable weaver, the costs and benefits of sociality are usually studied during the breeding period. This study shows that a better understanding of non‐breeding benefits of group membership and group dynamics between the non‐breeding and breeding periods are necessary for a comprehensive understanding of the benefits of sociality.     

Are clownfish groups composed of close relatives? An analysis of microsatellite DNA variation in Amphiprion percula

A central question of evolutionary ecology is: why do animals live in groups? Answering this question requires that the costs and benefits of group living are measured from the perspective of each individual in the group. This, in turn, requires that the group's genetic structure is elucidated, because genetic relatedness can modulate the individuals’ costs and benefits. The clown anemonefish, Amphiprion percula, lives in groups composed of a breeding pair and zero to four nonbreeders. Both breeders and nonbreeders stand to gain by associating with relatives: breeders might prefer to tolerate nonbreeders that are relatives because there is little chance that relatives will survive to breed elsewhere; nonbreeders might prefer to associate with breeders that are relatives because of the potential to accrue indirect genetic benefits by enhancing anemone and, consequently, breeder fitness. Given the potential benefits of associating with relatives, we use microsatellite loci to investigate whether or not individuals within groups of A. percula are related. We develop seven polymorphic microsatellite loci, with a number of alleles (range 2–24) and an observed level of heterozygosity (mean = 0.5936) sufficient to assess fine‐scale genetic structure. The mean coefficient of relatedness among group members is 0.00 ± 0.10 (n = 9 groups), and there are no surprising patterns in the distribution of pairwise relatedness. We conclude that A. percula live in groups of unrelated individuals. This study lays the foundation for further investigations of behavioural, population and community ecology of anemonefishes which are emerging as model systems for evolutionary ecology in the marine environment.     

Maintenance of Multifemale Social Organization in a Group of <Emphasis Type="Italic">Nomascus concolor</Emphasis> at Wuliang Mountain,Yunnan, China

Many short-term studies have reported groups of black crested gibbons containing ≥2 adult females (Nomascus concolor). We report the stability of multifemale groups in this species over a period of 6 yr. Our focal group and 2 neighboring groups included 2 breeding females between March 2003 and June 2009. We also habituated 1 multifemale group to observers and present detailed information concerning their social relationships over a 9-mo observation period. We investigated interindividual distances and agonistic behavior among the 5 group members. The spatial relationship between the 3 adult members (1 male, 2 females) formed an equilateral triangle. A subadult male was peripheral to the focal group, while a juvenile male maintained a closer spatial relationship with the adult members. We observed little agonistic behavior among the adult members. The close spatial relationship and lack of high rates of agonistic behavior among females suggest that the benefits of living in a multifemale group were equal to or greater than the costs for both females, given their ecological and social circumstances. The focal group occupied a large home range that was likely to provide sufficient food sources for the 2 females and their offspring. Between March 2003 and June 2009, 1 adult female gave 2 births and the other one gave 1 birth. All individuals in the focal group survived to June 2009. A long-term comparative study focused on females living in multifemale groups and females living in pair-living groups would provide insight into understanding the evolutionary mechanisms of the social system in gibbons.     

The cost of being alone: the fate of floaters in a population of cooperatively breeding pied babblers Turdoides bicolor

The occurrence of group-living behaviour has often been explained by the benefits individuals receive through cooperation; including increased reproductive output, vigilance against predators, and load-lightening behaviour. However, to fully understand the benefits of group-living, it is important to quantify the costs of living alone. Here, we look at the fate of floaters (individuals who have no fixed territory and remain alone for extended periods) in a population of cooperatively breeding pied babblers Turdoides bicolor . We found that individuals spent less time foraging and more time vigilant for predators when found as a floater compared to when they were in a group. Consequently, they suffered a continuous loss of body mass, with long-term floaters suffering the highest losses. This had a long-term effect: floaters that eventually did regain a position in a group usually entered as helpers, in contrast to dispersers, who usually entered a new group as breeders. This high cost of living alone highlights the benefits of group-living and may help to understand patterns of delayed dispersal in some social species.     

群居动物中的共同决策

群居的个体能够更好的躲避天敌的捕食,增强与同种其它种群的资源竞争,增加生殖机会与生殖成功率,使信息在个体之间顺畅的交流等。但是群内个体又会在有限的资源下产生群内的个体竞争,从而引起动物群的分裂,失去群居的利益。为了保持动物群的聚合力,当动物群内出现冲突时,需要在群内个体间形成协调各种冲突以及在群内达成共识的机制。依据动物社群组成的不同,领导力机制和自组织机制是协调群内冲突,形成一致决策和联合决策的两种主要机制。从行为生态学的角度入手,阐述了动物群内共同决策的类型,群内冲突的协调机制,共同决策的制定过程,比较了信息因素与利益因素在共同决策制定过程中的影响。旨在藉此推进我国相关领域研究的开展, 为群居动物社会与行为生态学研究者启发思路,并为保护群居濒危物种提供科学依据。     

Translocation as a novel approach to study effects of a new breeding habitat on reproductive output in wild birds

Environmental conditions under which species reproduce have major consequences on breeding success and subsequent fitness. Therefore breeding habitat choice is ultimately important. Studies rarely address the potential fitness pay-offs of alternative natural breeding habitats by experimental translocation. Here we present a new tool to study fitness consequences of free living birds in different habitats. We translocated a migratory passerine, the pied flycatcher (Ficedula hypoleuca), to a novel site, where pairs were subjected to a short stay (2-4 days) in a nest box-equipped aviary before being released. We show that it is technically possible to retain birds in the new area for breeding, allowing the study of reproductive consequences of dispersal under natural conditions. The translocation resulted in an extension of the interval between arrival and egg laying of four days, highlighting the importance of having an adequate control group. Clutch size and nestling parameters did not differ significantly between translocated and unmanipulated females, which suggests that the procedure did not affect birds in their reproductive performance later on. This method could be applied broadly in evolutionary and ecological research, e.g., to study the potential fitness benefits and costs for dispersing to more northern latitudes as a way of adapting to climate change.     

Age-specific cost of first reproduction in female southern elephant seals

When to commence breeding is a crucial life-history decision that may be the most important determinant of an individual''s lifetime reproductive output and can have major consequences on population dynamics. The age at which individuals first reproduce is an important factor influencing the intensity of potential costs (e.g. reduced survival) involved in the first breeding event. However, quantifying age-related variation in the cost of first reproduction in wild animals remains challenging because of the difficulty in reliably recording the first breeding event. Here, using a multi-event capture–recapture model that accounts for both imperfect detection and uncertainty in the breeding status on an 18-year dataset involving 6637 individuals, we estimated age and state-specific survival of female elephant seals (Mirounga leonina) in the declining Macquarie Island population. We detected a clear cost of first reproduction on survival. This cost was higher for both younger first-time breeders and older first-time breeders compared with females recruiting at age four, the overall mean age at first reproduction. Neither earlier primiparity nor delaying primiparity appear to confer any evolutionary advantage, rather the optimal strategy seems to be to start breeding at a single age, 4 years.     

Forcible eviction and prevention of recruitment in the clown anemonefish

How big an animal group will be depends on how the group's sizeis regulated and on the costs and benefits of living in thegroup. To determine which individuals regulate group size ofthe clown anemonefish, Amphiprion percula, I investigated thestrategies involved in the formation, maintenance, and dissolutionof its groups. Groups composed of a single breeding pair andof zero to four nonbreeding subordinates occupied individualsea anemones (Heteractis magnifica), which provided the fishwith oviposition sites and protection from predators. Groupsize increased linearly with anemone size. I used the residualsof this relationship as a measure of the degree of saturationof each anemone. Residents evicted low-rank subordinates andprevented the recruitment of additional subordinates at anemoneswith a high degree of saturation, but not at anemones with alow degree of saturation. These strategies indicate that residentscontrol group membership of their subordinates, and suggestthat residents might incur costs from the presence of subordinatesin more saturated anemones. In general, whenever residents cancontrol group membership, the prevention of recruitment andthe eviction of subordinates will set an upper limit on groupsize.     

Communal defense of territories and the evolution of sociality

The evolution of group living has attracted considerable attention from behavioral ecologists working on a wide range of study species. However, theoretical research in this field has been largely focused on cooperative breeders. We extend this line of work to species that lack alloparental care (hereafter termed "noncooperative species") but that may benefit from grouping by jointly defending a common territory. We adopt a demographically explicit approach in which the rates of births and deaths as well as the dispersal decisions of individuals in the population determine the turnover rates of territories and the competition for breeding vacancies thus arising. Our results reveal that some of the factors thought to affect the evolution of cooperative breeding also affect the evolution of group living in noncooperative species. Specifically, high fecundity and low mortality of resident individuals both increase the degree of habitat saturation and make joining an established group more profitable for nonresidents (floaters). Moreover, if floaters can forcefully take over territories, the degree of habitat saturation also affects the chance that residents become targets of takeovers. In this situation, communal defense of territories becomes an important benefit that further promotes the evolution of group living.     

Evolution of positive and negative density-dependent dispersal

Understanding the evolution of density-dependent dispersal strategies has been a major challenge for evolutionary ecologists. Some existing models suggest that selection should favour positive and others negative density-dependence in dispersal. Here, we develop a general model that shows how and why selection may shift from positive to negative density-dependence in response to key ecological factors, in particular the temporal stability of the environment. We find that in temporally stable environments, particularly with low dispersal costs and large group sizes, habitat heterogeneity selects for negative density-dependent dispersal, whereas in temporally variable environments, particularly with high dispersal costs and small group sizes, habitat heterogeneity selects for positive density-dependent dispersal. This shift reflects the changing balance between the greater competition for breeding opportunities in more productive patches, versus the greater long-term value of offspring that establish themselves there, the latter being very sensitive to the temporal stability of the environment. In general, dispersal of individuals out of low-density patches is much more sensitive to habitat heterogeneity than is dispersal out of high-density patches.     

Ecological,Evolutionary and Social Constraints on Reproductive Effort: Are Hoary Marmots Really Biennial Breeders?

Biennial breeding is a rare life-history trait observed in animal species living in harsh, unproductive environments. This reproductive pattern is thought to occur in 10 of 14 species in the genus Marmota, making marmots useful model organisms for studying its ecological and evolutionary implications. Biennial breeding in marmots has been described as an obligate pattern which evolved as a mechanism to mitigate the energetic costs of reproduction (Evolved Constraint hypothesis). However, recent anecdotal evidence suggests that it is a facultative pattern controlled by annual variation in climate and food availability (Environmental Constraint hypothesis). Finally, in social animals like marmots, biennial breeding could result from reproductive competition between females within social groups (Social Constraint hypothesis). We evaluated these three hypotheses using mark-recapture data from an 8-year study of hoary marmot (Marmota caligata) population dynamics in the Yukon. Annual variation in breeding probability was modeled using multi-state mark-recapture models, while other reproductive life-history traits were modeled with generalized linear mixed models. Hoary marmots were neither obligate nor facultative biennial breeders, and breeding probability was insensitive to evolved, environmental, or social factors. However, newly mature females were significantly less likely to breed than older individuals. Annual breeding did not result in increased mortality. Female survival and, to a lesser extent, average fecundity were correlated with winter climate, as indexed by the Pacific Decadal Oscillation. Hoary marmots are less conservative breeders than previously believed, and the evidence for biennial breeding throughout Marmota, and in other arctic/alpine/antarctic animals, should be re-examined. Prediction of future population dynamics requires an accurate understanding of life history strategies, and of how life history traits allow animals to cope with changes in weather and other demographic influences.     

Assessing the cost of mounting an immune response

The evolution of parasite resistance has often been assumed to be governed by antagonistic selection pressures. Defense against pathogens, by mounting an immune response, confers evident benefits but may also incur costs, so that the optimal level of defense is expected to depend on the balance between benefits and costs. Although the benefits of immune surveillance are well known, estimates of costs are still equivocal. Here we studied the behavioral and physiological modifications associated with exposure to a nonreplicating antigen (lipopolysaccharide [LPS] of Escherichia coli) in a passerine species, the house sparrow (Passer domesticus). We further investigated whether the behavioral and physiological changes provoked by LPS induced measurable repercussions on life-history traits, such as the breeding effort and reproductive success. Finally, we tested whether the trade-off between immune activation and breeding effort was modulated by the workload required to feed the brood. Exposure to LPS reduced activity and increased body mass loss of captive individuals; similarly, LPS injection induced a dramatic drop in feeding rate and reproductive success of breeding females. However, this reduction depended on brood size, suggesting that the strength of the trade-off between immune activation and reproduction was affected by the workload required to feed the brood. Overall, this study stresses the magnitude of costs associated with mounting immune responses and the ecological and evolutionary consequences for natural populations.     

Ecological and Social Determinants of Group Cohesiveness and Within‐Group Spatial Position in Wild Assamese Macaques

Individual spatial positioning plays an important role in mediating the costs and benefits of group living and, as such, shapes different aspects of animal social systems including group structure and cohesiveness. Here, we aim to quantify variation in individual spacing behaviour and its correlates in a group of wild Assamese macaques (Macaca assamensis) in north‐eastern Thailand, which experiences both predation pressure and within‐group feeding competition. Data on individual spatial positions were collected during group scans using GPS devices and results suggest that both group cohesiveness and individual spatial positions within a group can be adjusted to mediate the costs and benefits of group living. Individuals had greater nearest neighbour distances and lower numbers of close neighbours when the group was feeding, compared to when the main group activity was resting/social or moving. This is likely due to the high costs of proximity associated with feeding competition. Immature individuals and females with young infants which are more vulnerable to predation were located closer to the centre of the group than both adult males and females without infants. This indicates the importance of predation risk in driving individual spatial position. Among adults, higher ranking individuals occupied more central positions within the group while lower ranking individuals were more peripheral. It appears that low ranking individuals trade reduced feeding interference and improved feeding success for increased predation risk. This could help explain why females in the study population do not display a rank related skew in energy intake.     

Net costs of group living in a solitary forager, the Eurasian badger (Meles meles)

Group living is expected to evolve under two extreme conditions:when there are net benefits to the individual of living in agroup and when there are net costs to living in a group togetherwith strong ecological constraints on dispersal and independentbreeding. A third condition may facilitate group formation:when the territorial defense of resources that are dispersedwidely or renewed at high rates allows groups to form at nocost to group members. Eurasian badgers are solitary over alarge part of their geographic distribution and forage aloneeven where diey live in territorial groups. To determine whichof the three conditions best explains group living in badgers,we analyzed dispersal and breeding patterns. Using these datawe describe the mechanism of group formation and the net costsor benefits of group living in 16 badger groups in one population.Groups form primarily by the retention of young on their natalterritory. Typically, groups contain one or more sexually maturebut nonbreeding females in addition to one or more breedingfemales. Females do not benefit from group living as indicatedby the lack of relationships, or perhaps negative relationships,between the proportion of adult females that bred in a groupand mean reproductive success, on the one hand, and group sizeand components of group size, on the other. A high reproductivefailure rate among females in this and other populations ofsocial badgers, as compared with a population of solitary badgers,suggests that there is a cost of group living to females. Wepropose that if badgers defend resources whose spatial distributionor high renewal rates allow groups to form on a territory atlitde or no cost to group members, weak ecological constraintson dispersal and independent breeding are sufficient to explainthe formation of groups. Badgers appear to have not evolvedcooperative breeding in response to these ecological conditions,perhaps because badger groups represent an early stage in theevolution of carnivore sociality.     

Cooperative breeding shapes post‐fledging survival in an Afrotropical forest bird

For avian group living to be evolutionary stable, multiple fitness benefits are expected. Yet, the difficulty of tracking fledglings, and thus estimating their survival rates, limits our knowledge on how such benefits may manifest postfledging. We radio‐tagged breeding females of the Afrotropical cooperatively breeding Placid greenbul (Phyllastrephus placidus) during nesting. Tracking these females after fledging permitted us to locate juvenile birds, their parents, and any helpers present and to build individual fledgling resighting datasets without incurring mortality costs or causing premature fledging due to handling or transmitter effects. A Bayesian framework was used to infer age‐specific mortality rates in relation to group size, fledging date, maternal condition, and nestling condition. Postfledging survival was positively related to group size, with fledglings raised in groups with four helpers showing nearly 30% higher survival until independence compared with pair‐only offspring, independent of fledging date, maternal condition or nestling condition. Our results demonstrate the importance of studying the early dependency period just after fledging when assessing presumed benefits of cooperative breeding. While studying small, mobile organisms after they leave the nest remains highly challenging, we argue that the telemetric approach proposed here may be a broadly applicable method to obtain unbiased estimates of postfledging survival.     

Habitat suitability and the constraints of migration in New World warblers

Identifying the factors that influence geographic range limits can illustrate the various ecological, physiological, and evolutionary constraints imposed on a species. The range limits of migratory birds are particularly challenging to study as they occur in disjunct regions at different times of the year, which can impose different constraints. Travel between breeding and wintering regions poses a significant energetic and navigational challenge to birds, although it is not clear how these movements influence breeding dispersal and range expansion. Here I ask whether the possible costs of migration limit the breeding ranges of wood warblers, a group of birds with an extensive history of ecological and evolutionary studies. I used occurrence records for multiple wood warbler species, breeding primarily in the boreal forest of North America, to generate environmental niche models. I tested for over‐prediction of habitat suitability into the western boreal forest, where most these species do not have occurrence records but where there is presumably suitable habitat. I found that some of these vagile taxa, primarily found east of the Rocky Mountains, also have predicted habitat suitability that extends into the north and west, where they have little to no occurrence records. I discuss several possible explanations for this discordance. In particular, the patterns are consistent with the costs of a long‐distance migration limiting the benefits of range expansion, as migration may become too onerous as the distance between breeding and wintering areas increases. These results speak to the process of niche filling more generally and call attention to an under‐appreciated explanation for why migratory species may not fully occupy their fundamental niche.     

The adaptive value of energy storage and capital breeding in seasonal environments

Timing of reproduction in a seasonal cycle is a life history trait with important fitness consequences. Capital breeders produce offspring from stored resources and, by decoupling feeding and reproduction, may bend the constraints caused by seasonality in food or predation. Income breeders, on the other hand, produce offspring from concurrent food intake, with the disadvantage of less flexibility, but with high efficiency and no inventory costs of carrying stores. Here, we assess relative profitability of capital and income breeding in herbivorous zooplankton inhabiting seasonal, high-latitude environments. We apply a state-dependent life history model where reproductive values are used to optimise energy allocation and diapause strategies over the year. Three environmental scenarios were modelled: an early, an intermediate, and a late feeding season. We found that capital breeding was most important in the early season. Capital breeding ranged from 7–9% of the eggs produced but, because of the high reproductive value of early eggs, capital breeding ranged from 9–30% when measured in terms of reproductive value. The main benefit of capital breeding was reproduction prior to the feeding season – when the reproductive value of an egg peaked. In addition, capital breeding was also used to increase egg production rates at times of income breeding. For individuals born late in the season the model predicted a two-year cycle instead of the typical annual life cycle. These individuals could then reap the benefits of early reproduction and capital breeding in their second year instead of income breeding late in the first year. We emphasize the importance of evaluating reproductive strategies such as capital and income breeding from a complete life cycle perspective. In particular, knowing the seasonality in offspring fitness is essential to appreciate evolutionary and population-level consequences of capital breeding.     

Evidence of helping behavior in a free-ranging population of communally breeding warthogs

Cooperative breeding societies are defined by the presence of helpers. Defining helping behavior in cooperatively breeding mammals has been difficult because lactation limits the ability of individuals to provision non-genetic young. As a consequence, “helping” behavior has frequently included predator and conspecific defense and thermoregulation. However, these behaviors are often associated with the benefits of group living and their expression may not warrant a species’ classification as a cooperative breeder (e.g., many ungulates and pinnipeds). In this study, we examine cooperative breeding behavior in the common warthog, Phacochoerus africanus. Warthogs exhibit substantial variation in breeding strategies and females will raise their young alone or in association with other females. The size of warthog groups varies throughout the year and we investigate fission and fusion of individual breeding groups to elucidate the costs and benefits of adopting different reproductive strategies. We found that the cohesion of female groups was related to parturition suggesting that there are benefits to sociality that are related to the production and care of offspring. Additionally, we found that reproductively-aged group members will help other group members by both babysitting and adopting the group’s offspring indicating active selection for cooperation. We did not witness any incidences of yearling group members exhibiting these behaviors indicating differential trade-offs to cooperation possibly related to the helper’s age/experience.     

Metabolic correlates of leg length in breeding arctic shorebirds: the cost of getting high

Aim We test the hypothesis that tarsus length in all shorebirds breeding in the Canadian arctic shows an evolutionary response to average metabolic stress encountered across the breeding range, such that birds nesting in metabolically stressful environments have relatively shorter legs. Longer‐legged birds living in colder environments will experience greater metabolic costs because their torsos are elevated farther away from the ground's wind‐dampening boundary layer. Methods We use weather data (temperature, wind speed, global solar radiation) from 27 arctic weather stations measured over 37 years, and a previously published model of heat transfer, to characterize the metabolic harshness over the breeding season of the ranges of each of the 17 shorebirds of the family Charadriidae nesting in the Canadian arctic. Results After controlling for the lengths of two other body extremities (wing and bill), there was a significant negative relationship between tarsus length and mean metabolic harshness. This result was obtained whether species were treated as independent data points, or in a comparative analysis using standardized independent contrasts. Main conclusions We support a unique extension of Allen's rule: body‐supporting appendages of homeotherms may be shorter in colder environments so as to take advantage of a boundary layer effect, thereby reducing metabolic costs.     

Natal dispersal in great bustards: the effect of sex, local population size and spatial isolation

1. We investigated the causes of natal dispersal in four Spanish areas where 35 breeding groups of the polygynous great bustard Otis tarda were monitored intensively. A total of 392 juveniles were radio-tracked between 1991 and 2006 by ground and via aeroplane to avoid potential biases derived from the non-detection of long-distance dispersers. 2. We explored 10 explanatory variables that were related to individual phenotypic features, habitat and conspecific traits in terms of group size and breeding performance, and spatial distribution of available breeding groups. Probability of group change and natal dispersal distances were investigated separately through multifactorial analyses. 3. Natal dispersal occurred in 47.8% of the birds and median natal dispersal distance of dispersers was 18.1 km (range 4.97-178.42 km). Sex largely determined the dispersal probability, with 75.6% of males being dispersers and 80.0% of females being philopatric, in contrast to the general pattern of female-biased dispersal found in most avian species. 4. Both the frequency of natal dispersal and dispersal distances were affected by the spatial distribution of breeding groups. More isolated groups showed a higher proportion of philopatric individuals, the effect being more evident in males than in females. This implies a reduction in gene flow in fragmented populations, as most genetic exchange is achieved through male dispersal. Additionally, dispersers hatched in more isolated groups tended to exhibit longer dispersal distances, which increases the associated energetic costs and mortality risks. 5. The dispersal decision was influenced by the number of conspecifics in the natal group. The individual probability of natal dispersal was related inversely to the size of the natal group, which supports the balanced dispersal model and the conspecific attraction hypothesis. 6. Overall, our results provide a good example of phenotypic plasticity and reinforce the current view that dispersal is an evolutionary complex trait conditioned by the interaction of individual, social and environmental causes that vary between individuals and populations.