Polygyny and its fitness consequences for primary and secondary female pied flycatchers

In polygynous species with biparental care, the amount of paternal support often varies considerably. In the pied flycatcher (Ficedula hypoleuca), females mated with monogamous males receive more male assistance during the nestling phase than females mated with bigynous males, as the latter have to share their mates with another female. Bigynous males, however, give more support to their primary broods than to their secondary broods. Using a long-term dataset (31 years), the present study revealed that direct reproductive success, i.e. number of fledglings, was lower in females that mated with bigynous males, especially in secondary broods without male assistance, than in females that mated with monogamous males. Secondary broods with male assistance were more affected than primary broods. Female survival was independent of mating status. In primary broods, a delayed compensation for inferior direct reproductive success was found in terms of the number of grandoffspring, a phenomenon that did not occur in secondary broods. Delayed compensation in primary broods refers to indirect effects, i.e. good genes. According to the sexy son hypothesis, genetically superior (i.e. sexy) males may have sons with a higher number of broods belonging to a polygynous breeding status than do sons from broods with a monogamous father. This was indeed the case for sons descending from primary broods, but not for sons descending from secondary broods.     

Polygyny in the yellow-headed blackbird: female choice versus male competition

Several assumptions and predictions of the polygyny threshold and sexy son hypotheses, which were proposed to explain the maintenance of polygyny on the basis of female choice, were examined. An alternative neutral mate choice hypothesis in which male competition is responsible for polygyny was also examined. For the yellow-headed blackbird, Xanthocephalus xanthocephalus, neither territory nor male features affected female choice of mate or female reproductive success. In the study population, polygyny occurred because males competed to hold territories in order to gain access to females. Since females settled apparently randomly, males that were more aggreessive and were therefore able to secure large territories had larger harems. Several criteria must be met in order for the neutral mate choice hypothesis to apply. Evidence from the literature suggests that for some species the criteria are not met and polygyny occurs due to female choice. However, several studies provide evidence that the neutral mate choice hypothesis may apply in some populations.     

Polygyny in the pied flycatcher,Ficedula hypoleuca: a test of the deception hypothesis

The deception hypothesis has been proposed as an explanation for polygyny in the pied flycatcher. According to this hypothesis, already-mated males hide their mating status with polyterritorial behaviour and thereby increase their chances of obtaining a second mate. In a study area at Oslo, Norway, secondary females raised 84% as many fledglings as did concurrent monogamous and primary females. The unmated males sang most of the time near their nest site, whereas the already-mated males frequently disrupted singing for longer periods in their secondary territories to visit their primary nest; such visits to the primary nest occurred both before and after the time of their second mating. The behaviour of the males suggests that deception of females is not an evolutionarily stable strategy, as an observant female would soon discern the male's status. Another difficulty with the deception hypothesis is that secondary females laid larger clutches than primary females. The number of young fledged from secondary nests was not dependent on the distance to the primary nest. The deception hypothesis was not supported by the data, and the reduced reproductive success of secondary females may be explained by the cost of searching for a mate.     

Social mating system and reproductive success in house wrens

Current models explaining the establishment and maintenanceof social monogamy and polygyny within avian populations typicallyassume that the reproductive success of polygynous males exceedsthat of monogamous males. This assumption is almost always supportedwhen the number of fledglings or recruits to future breedingpopulations is used to measure adult reproductive success. However,recent studies using DNA markers indicate that simple countsof fledglings or recruits may be a poor estimator of the numberof nestlings sired by the social father. In this paper, we comparethe number of genetic offspring produced by socially monogamousand polygynous house wren (TrogiodyUs atdon) males in nestsat which they were the social father. Polygynous males did,in fact, sire more nestlings in their own nests than did monogamousmales. Moreover, although we have not identified the sires ofextrapair nestlings, we document that even when all extrapairnestlings in this population are hypotheticaOy assigned to monogamousmales, die total reproductive success of polygynous males exceedsthat of monogamous males. These results and those of severalother recent studies are consistent with the assumption thatpolygynous males produce more offspring than monogamous males.     

A test of the "sexy son" hypothesis: sons of polygynous collared flycatchers do not inherit their fathers' mating status

According to the original "sexy son" hypothesis, a female may benefit from pairing with an already-mated male despite a reduction in fecundity because her sons inherit their father's attractiveness. We used data from a long-term study of collared flycatchers (Ficedula albicollis) collected during 24 years to test this prediction. Our results show that the sons of polygynously mated females fledged in poor condition and therefore did not inherit their father's large forehead patch (a condition-dependent display trait) or mating status. From the female's perspective, polygynous pairing resulted in fewer recruited grandchildren than did a monogamous pairing. The reproductive value of sons did not outweigh the fecundity costs of polygyny because the low paternal care reduced the attractiveness of sons. When there are long-lasting parental effects on offspring attractiveness, costs of polygyny may include the production of nonsexy sons.     

Territorial polygyny in house wrens: are females sufficiently compensated for the cost of mate sharing?

We tested two hypotheses to explain the occurrence of polygynyin a box-nesting population of the house wren (Troglodytes aedon),a small, insectivorous songbird. Some proportion of femalesin this population routinely settle with already-mated maleseven though unmated males hold territories relatively shortdistances away. The "polygyny-threshold" hypothesis proposesthat mated males possess territorial resources that compensatefemales for the cost of mate sharing (i.e., reduced aid in feedingyoung). Contrary to a key prediction of this hypothesis, however,we found that secondary females produced fewer offspring thanfemales who chose nearby unmated males. The "sexy son" hypothesisproposes that mated males father attractive, prolific sons,which results in secondary females obtaining as many grandoffspringas expected had they chosen available unmated males. Our datasuggest that if male mating success is at least moderately heritable,secondary females may produce enough fledglings per breedingattempt relative to their monogamously mating counterparts torecoup fitness losses in the next generation. However, fullacceptance of this hypothesis must await confirmation that malemating success is heritable. We suggest a third hypothesisfor why females readily mate polygynously when better, monogamousbreeding options are clearly available. We argue that femalesmay choose mated males because these males possess highquality nest sites (i.e., nest-boxes), and that access to such nestsites would provide females with sufficient compensation forthe costs of polygyny under normal conditions when all availableunmated males would have poorer-quality, natural nest sites.This "expected compensation" hypothesis assumes that polygynouslymating females terminate mate search before they discover thatavailable unmated males also possess nestboxes. A recent theoreticalexploration of mate search strategy suggests that this assumptionis reasonable.     

Breeding Biology and Variable Mating System of a Population of Introduced Dunnocks (Prunella modularis) in New Zealand

Species with variable mating systems provide a unique opportunity to investigate whether females receive direct fitness benefits from additional male partners. The direct benefits provide an obvious explanation for why females would breed polyandrously, in a situation where males clearly do not attain their optimal reproductive success. Evidence for these direct benefits is, however, mixed. Here, we present a detailed study of the breeding biology of the dunnock, Prunella modularis, which inform an investigation into the effects of the social mating system on the reproductive success in a population of dunnocks in Southern New Zealand. We studied 80 different social groups over the course of three breeding seasons. Dunnocks in our population presented a variable mating system, with socially monogamous (45%), socially polyandrous (54%) and socially polygynandrous (1%) groups being observed in the same breeding season. We did not observe any polygynous social units in our study period although polygyny exists in the population. We found little difference in the numbers of eggs laid, and egg volume between monogamous and polyandrous nests. However, polyandrous groups had better hatching and fledging success than monogamous groups (composite d = 0.385, 95% CI: 0.307 to 0.463). Overall our results support the notion that polyandry is beneficial for females.     

Extra-pair paternity in monogamous and polygynous Savannah sparrows,Passerculus sandwichensis

Extra-pair paternity can influence mating systems by affecting the fitness costs associated with polygyny. Polygyny is disadvantageous to males when the time and energetic demands of multiple pairings decrease either a male's success at gaining extra-pair fertilizations or his ability to ensure paternity among harem members. In Savannah sparrows,Passerculus sandwichensison Kent Island, New Brunswick, Canada, multilocus DNA fingerprinting of 136 adults and young revealed substantial female infidelity: overall, 31 of 92 young (33.7%) in 15 of 24 nests (62.5%) were the product of extra-pair fertilizations. Male mating status was a strong predictor of paternity. Each of seven monogamous females produced at least one extra-pair offspring, but only six of 11 primary females (54.5%) and two of six secondary females (33.3%) were unfaithful. As a result, nearly 80% of the young in nests of polygynous males resulted from within-pair fertilizations, compared with only 40% of the young in nests of monogamous males. Kent Island Savannah sparrows are simultaneously polygynous, and the absence of paternity costs associated with polygyny is surprising. The observed pattern of paternity suggests the operation of female choice, although male control of parentage cannot be excluded.     

HERITABILITY AND SELECTION ON TARSUS LENGTH IN THE PIED FLYCATCHER (FICEDULA HYPOLEUCA)

The heritability estimate (±SE) for tarsus length in the pied flycatcher is 0.53 ± 0.10, based on mother-offspring regressions. The heritability is almost the same (0.50 ± 0.22) for offspring transferred to other nests and reared by foster parents, whereas there is no resemblance (0.04 ± 0.23) between the offspring and their foster mothers. Hence, the nest environment does not affect parent-offspring resemblance. However, a full-sib correlation yields an estimate of the heritability twice as high as the parent-offspring regression did, indicating that shared environment effects, which are not correlated with the tarsus length of parents, must be important. An environmental deviation due to food factors affecting tarsus length is demonstrated. The most important food factors are probably associated with 1) polygyny, which leads to reduced paternal feeding at secondary nests, 2) high breeding density, and 3) progress of the breeding season. All three are associated with reductions in offspring mean tarsus length. We estimate selection on tarsus length for the major components of lifetime reproductive success. Offspring with the shortest tarsi have reduced survival from fledging until breeding, and males with tarsus length close to the mean are most successful in attracting mates. Clutch size increases with female tarsus length, except for individuals with very long tarsi. In general, directional selection is weak, but stabilizing selection is rather strong for survival and male mating success.     

Why do pied flycatcher females mate with already-mated males?

The contribution of the pied flycatcher Ficedula hypoleuca male in parental care was studied to examine why some females mate with already-mated males. No difference in feeding rate was found between older and yearling monogamous males, when comparing nests at the same time. Monogamous and primary females were helped significantly more in parental care by the male than were secondary females of polygynous males. Females could only partly compensate for the absence of a male and of nestlings were reduced in nests with low male assistance. Differences in mate and territory quality were far too slight to make it advantageous for females to choose already-mated males instead of mating with monogamous males. We suggest that males, by being polyterritorial, deceive females into accepting polygyny; and females can be deceived since they do not have time to find out the marital status of males.     

Is offspring dispersal related to male mating status? An experiment with the facultatively polygynous spotless starling

Patterns of natal dispersal are generally sex‐biased in vertebrates, i.e. female‐biased in birds and male‐biased in mammals. Interphyletic comparisons in mammals suggest that male‐biased dispersal occurs in polygynous and promiscuous species where local mate competition among males exceeds local resource competition among females. However, few studies have analysed sex‐biased patterns of dispersal at the individual level, and facultatively polygynous species might offer this opportunity. In the spotless starling, polygynous males exhibit their mating status during courtship carrying higher amounts of green plants to nests than monogamous males. We experimentally incorporated green plants to nests during four years to analyse long‐term consequences on breeding success and offspring recruitment rates. We unexpectedly found that experimental sons recruited farther than experimental daughters, while control daughters recruited farther than control sons. A similar pattern was found using observational information from eight years. We discuss this result in the context of local competition hypothesis and speculate that sons dispersed farther from nests controlled by polygynous males to avoid competition with relatives. The amount of green plants in nests affects female perception of male attractiveness and degree of polygyny, although little is known about proximate mechanisms linking this process with the offspring dispersal behaviour. Our results support the idea that male‐biased dispersal is related to polygyny in a facultatively polygynous bird.     

Reproduction and survival of polygynous and monogamous Blue Tit Parus caeruleus

In a seven-year study of Blue Tits in optimal habitat near Antwerp, Belgium, 45 polygynous broods involving 22 males out of 667 successful first broods were found. In another 43 nests no male was found, although a major effort was made to trap all adults. The estimated proportion of polygynous males is 3.4%, if only confirmed cases are considered, but 10.8% if all possible cases are included. One male was paired simultaneously to three females.
Primary females (laying earliest in a triangle) were as successful as monogamous ones. Secondary (laying later in a triangle) and deserted females (nests in which no male was trapped), although still quite successful, raised fewer young and in one plot had a lower probability of recruiting offspring.
Both in males and females, the frequency of polygyny was independent of age. Adult survival did not differ between monogamous and polygynous males. Among females no effect of pairing status on survival was found in one plot, but in a second plot monogamous females survived better than others. It is concluded that in any study of Blue Tits in optimal habitat one could expect to find polygyny.     

Genetic monogamy in single-male groups of acorn woodpeckers, Melanerpes formicivorus

Acorn woodpeckers have one of the most complex social systems of any bird species. Breeding units range in size from monogamous pairs to groups of 15 birds that include multiple breeding males and females as well as nonreproductive helpers-at-the-nest. Groups form when young remain at their natal nest to help their parents breed or when single-sex coalitions of siblings disperse to fill a reproductive vacancy on another territory. Plural breeding and helping behaviour are thought to be favoured through indirect fitness benefits for individuals that would otherwise be unable to breed due to a shortage of reproductive vacancies on territories with acorn stores. We report the results of multi-locus DNA fingerprinting of 51 offspring from 18 nests of 16 socially monogamous pairs of acorn woodpeckers. If socially monogamous females mate outside the pair-bond, indirect fitness benefits for cobreeders and helpers will be significantly reduced. Monogamous pairs accounted for all but one of the 51 offspring we tested; the single exception was apparently sired by the putative father, but the putative mother was excluded from maternity. Our results indicate that individuals remaining on their natal territories as helpers are generally the genetic offspring of the pair they help. They also suggest that single-sex coalitions offspring dispersing together from nests of socially monogamous pairs will be full-siblings.     

A role for female ornamentation in the facultatively polygynous mating system of collared flycatchers

In a polygynous mating system, females settling with alreadymated males often experience low mating success due to the reducedparental contribution of the male. However, there are numerousfactors that may still make it advantageous for some femalesto choose this mating status. Facultative polygyny is believedto be dominated by male advertisement and female choice. Althoughquality differences and competition among females are increasinglyrecognized as important determinants of polygynous settlementpatterns, the importance of signals of female quality in thismating system is largely unknown. Here we examined the relationshipof the white wing patch size (WPS) of female collared flycatchers,a phenotypically plastic and age-dependent ornament, with socialmating status, while controlling for settlement date and age.At the population level, monogamous, primary, and secondaryfemales did not differ in WPS. However, the primary female ofindividual males was more ornamented than the secondary female,and this difference declined with increasing distance betweenprimary and secondary nests. Secondary female ornamentationincreased, whereas that of the primary female did not changewith nest distance. These results suggest a subtle role forfemale ornamentation at polygynous mating. Future studies shouldtherefore take into account mating status when assessing thecosts and benefits of female signals. Moreover, patterns inquality-indicating female traits may contribute to the explanationof differences in reproductive success among females of differentmating status.     

Paternal influence on growth and survival of dark-eyed junco young: do parental males benefit?

Recent studies of typically monogamous passerine birds have suggested that the fitness benefits males derive by caring for their young may not be as great as was previously thought. This study was conducted to determine whether parental care by male dark-eyed juncos, Junco hyemalis, serves to increase either the quantity or quality of young that they produce. Over a 4-year period, males were caught at the time their eggs hatched, and the subsequent growth and survival of the young of unaided females and control pairs were compared. Broods raised by unaided females gained body mass more slowly and fledged at slightly lower mass than those raised by two parents. However, fledging mass was not correlated with survival to independence. There were no differences in tarsus growth between the two treatment groups. Entire brood loss to predators occurred as often among females without male help as it did among those with male help. However, partial brood loss was more common among female-only broods than among controls; this difference was largely attributable to higher rates of starvation and exposure in female-only broods. There appeared to be an interaction between growth and predation. Female-only broods that were below the median mass of combined treatment groups at 5 days of age were more likely than all other broods to experience partial or complete predation. Male impact on offspring survival varied with age of the offspring. When years were combined, males tended to increase survival during the first half of the nestling period, but their impact at the time of nest-leaving was minimal. In all years, from nest-leaving to independence (ca. 2 weeks), broods without male help survived only about half as well as did those with male help. Independent young raised by one parent were as likely to return the following spring as were young raised by two parents. Thus, paternal care benefits males by improving the survivorship of their fledglings, and may also act as a buffer against poor female parental quality and inclement weather. However, the magnitude of these benefits is such that bigamous males might achieve greater reproductive success than monogamous males. Various possible male strategies are discussed.     

Experimental confirmation of the polygyny threshold model for red-winged blackbirds

The polygyny threshold model assumes that polygynous mating is costly to females and proposes that females pay the cost of polygyny only when compensated by obtaining a superior territory or male. We present, to the authors' knowledge, the first experimental field test to demonstrate that females trade mating status against territory quality as proposed by this hypothesis. Previous work has shown that female red-winged blackbirds (Agelaius phoeniceus) in Ontario prefer settling with unmated males and that this preference is adaptive because polygynous mating status lowers female reproductive success. Other evidence suggests that nesting over water increases the reproductive success of female red-winged blackbirds. Here we describe an experiment in which females were given choices between two adjacent territories, one owned by an unmated male without any over-water nesting sites and the other by an already-mated male with over-water sites. Females overwhelmingly preferred the already-mated males, demonstrating that superior territory quality can reverse preferences based on mating status and supporting the polygyny threshold model as the explanation for polygyny in this population.     

Genetic covariance between components of male reproductive success: within‐pair vs. extra‐pair paternity in song sparrows

The evolutionary trajectories of reproductive systems, including both male and female multiple mating and hence polygyny and polyandry, are expected to depend on the additive genetic variances and covariances in and among components of male reproductive success achieved through different reproductive tactics. However, genetic covariances among key components of male reproductive success have not been estimated in wild populations. We used comprehensive paternity data from socially monogamous but genetically polygynandrous song sparrows (Melospiza melodia) to estimate additive genetic variance and covariance in the total number of offspring a male sired per year outside his social pairings (i.e. his total extra‐pair reproductive success achieved through multiple mating) and his liability to sire offspring produced by his socially paired female (i.e. his success in defending within‐pair paternity). Both components of male fitness showed nonzero additive genetic variance, and the estimated genetic covariance was positive, implying that males with high additive genetic value for extra‐pair reproduction also have high additive genetic propensity to sire their socially paired female's offspring. There was consequently no evidence of a genetic or phenotypic trade‐off between male within‐pair paternity success and extra‐pair reproductive success. Such positive genetic covariance might be expected to facilitate ongoing evolution of polygyny and could also shape the ongoing evolution of polyandry through indirect selection.     

Division of labour during incubation in a woodpecker Colaptes auratus with reversed sex roles and facultative polyandry

The contribution of males to incubation has rarely been studied in altricial birds because the pursuit of extra mating opportunities is believed to conflict with incubation. Woodpeckers show reversed sex roles in parental care with males doing most of the nest construction, incubating and brooding of the young while females may be polyandrous. I investigated incubation by each sex at 71 monogamous and four polyandrous nests of the Northern Flicker Colaptes auratus , predicting that males would contribute to incubation according to their energy reserves (body condition) whereas females would contribute based on alternate reproductive opportunities. Nest attendance was 99% with males contributing a mean of 66% of the total incubation including nocturnal incubation. The length of daytime bouts averaged about 2 h and did not differ between the sexes. Consistent with predictions of investment strategies, structurally larger males and those in poorer body condition incubated less than smaller males, perhaps because they required more recess time to forage or to conserve energy. Older females contributed less incubation than young females and polyandrous females contributed less incubation at their secondary nests than monogamous females. Incubation period, nest depredation rate and hatching success were not influenced by bout length, number of bouts or relative contribution of the sexes. Hatching success was 86% at nests of both monogamous and polyandrous females because males compensated for reduced female participation. Because incubation of the sexes is compensatory and not additive, incubation pattern did not influence short-term reproductive success. I conclude that males invest in incubation according to their energy needs, and females may adjust their contributions based on alternate reproductive tactics.     

Males achieve greater reproductive success through multiple broods than through extrapair mating in house wrens

In polygynous species, it is unclear whether extrapair matings provide a better reproductive payoff to males than additional social mates. Male house wrens, Troglodytes aedon, show three types of social mating behaviour: single-brooded monogamy, sequential monogamy (two broods) and polygyny. Thus, male reproductive success can vary depending on the number of mates, the number of broods and the number of extrapair fertilizations. We used microsatellite markers to determine the realized reproductive success (total number of young sired from both within-pair and extrapair fertilizations) of males in these three categories. We found that polygynous males were more likely to be cuckolded than monogamous males; however, half of the polygynous males had a third brood, which resulted in similar reproductive success for sequentially monogamous and polygynous males. Despite the paternity gained from extrapair fertilizations by single-brooded males, males were more successful when they produced multiple broods during a season, either sequentially (monogamy) or simultaneously (polygyny). In our population, multibrooded males were more likely to have prior breeding experience and arrived earlier in the season, which provided a better opportunity to obtain more than one brood and, thus, produce more young.     

A test of the Darwin–Fisher theory for the evolution of male secondary sexual traits in monogamous birds

The Darwin–Fisher theory proposes that the presence of male secondary sexual traits in monogamous birds is selected for by early season breeding of females that are in good condition. These early breeding females have high fecundity because of their good condition, and they select mates based on secondary sex traits. We tested whether this hypothesis may be responsible for the presence of male sexual ornaments in the great frigatebird, a socially and genetically monogamous seabird. Consistent with the Darwin–Fisher theory, we found that reproductive success declined over the season. However, males with more exaggerated ornaments were not chosen as mates earlier in the season than males with less exaggerated ornaments, and selection gradients on these ornaments were not significantly different from zero.