Timing of prenuptial molt as a sexually selected indicator of male quality in superb fairy-wrens (Malurus cyaneus)

Seasonally dichromatic male superb fairy-wrens (Malurus cyaneus)solicit extra-group fertilizations through displays of theirbrightly colored nuptial plumage during visits to females inneighboring territories. This ornamental plumage is lost atthe end of the breeding season, and reacquired before the nextbreeding season after a highly variable period spent in a cryptic,female-like, "eclipse" plumage. Individuals start visiting femalesas soon as they return to nuptial plumage, often several monthsbefore the start of breeding.We examine variation in the timingof acquisition of nuptial plumage in relation to environmentalconditions and the age, social status, and condition of males.We show that males undergo the prenuptial molt earlier as theyage and when in superior condition, and that molt is delayedin years of more adverse winter weather conditions. We proposethat the purpose of male displays may be to advertise theirquality, and that females use this variation in the timing ofacquisition of nuptial plumage to assess the relative qualityof prospective extra-group mates. Molting earlier is apparentlycostlier, so this handicap would appear to be a reliable reflectionof male quality.     

Mate choice in Darwin's Finches

Female Geospiza conirostris on Isla Genovesa, Galapagos, pair preferentially with males who have had previous breeding experience. They choose mates on the basis of courtship behaviour and black adult plumage. By mating with experienced black males, they gain a fitness advantage in terms of fledgling production and recruitment of young into the breeding population. Behavioural signs of past breeding experience and black plumage are reliable age- and condition-dependent traits. We suggest that females use conspicuous black plumage to identify old males at a distance, then interactions through courtship to modify initial assessments. Females paired with inferior males may increase the genetic quality of their offspring by extra-pair copulations; results of heritability analysis of morphology are consistent with this suggestion. Females change mates at a frequency of 12–27% per breeding season. They re-pair with males who are generally old, experienced, and hold territories adjacent to the deserted male. Females that re-pair gain a benefit, whereas males who are deserted within a breeding season incur a cost of more than 50% of their future potential production for that season. We conclude that females in choosing males seek reliable indicators of potential parental care, and in addition they may seek indicators of genetic quality.     

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.     

Costs and benefits of variable breeding plumage in the red-backed fairy-wren

The red-backed fairy-wren is a socially monogamous passerine bird which exhibits two distinct types of breeding male, bright males that breed in bright red and black plumage and dull males that breed in dull brown plumage. Most males spend their first potential breeding season in dull plumage and subsequent breeding seasons in bright plumage, but a relatively small proportion of males develop bright plumage in their first breeding season. This study quantifies morphology, behavior, and reproductive success of dull and bright males to assess the adaptive costs and benefits of bright plumage while controlling for age. Older bright males (two years of age or older) attempted to increase their reproductive success via copulations with extrapair females, whereas younger (one-year old) bright males and dull males did not. Thus, older bright males spent less time on their own territories, intruded on neighboring groups with fertile females more frequently, gave more courtship displays, and had larger sperm storage organs than did younger bright males and dull males. Microsatellite analyses of paternity indicate that the red-backed fairy-wren has extremely high levels of sexual promiscuity, and that older bright males had higher within-brood paternity than dull males or younger bright males. Regardless of age, bright males were more attractive to females in controlled mate choice trials than were dull males, and both age classes of bright males obtained higher quality mates earlier in the breeding season than did dull males, when nesting success was higher. In conclusion, although it appears that bright plumage increases access to higher quality mates, age also plays a central role in determining a male's overall reproductive success because of the high levels of sexual promiscuity exhibited by the red-backed fairy-wren.     

Social mating systems and extrapair fertilizations in passerine birds

Two alternative hypotheses have been proposed to explain howsocial and genetic mating systems are interrelated in birds.According to the first (male trade-off) hypothesis, socialpolygyny should increase extrapair fertilizations because whenmales concentrate on attracting additional social mates, theycannot effectively protect females with whom they have already paired from being sexually assaulted. According to the second(female choice) hypothesis, social polygyny should decreaseextrapair fertilizations because a substantial proportion offemales can pair with the male of their choice, and males caneffectively guard each mate during her fertile period. To discriminatethese alternatives, we comprehensively reviewed informationon social mating systems and extrapair fertilizations in temperatezone passerine birds. We found significant inverse relationshipsbetween proportions of socially polygynous males and frequenciesof extrapair young, whether each species was considered asan independent data point (using parametric statistics) orphylogenetically related species were treated as nonindependent (using contrasts analyses). When social mating systems weredichotomized, extrapair chicks were twice as frequent in monogamousas in polygynous species (0.23 vs. 0.11). We hypothesize thatin socially polygynous species, (1) there is less incentivefor females and males to pursue extrapair matings and (2) femalesincur higher costs for sexual infidelity (e.g., due to physical retaliation or reduction of paternal efforts) than in sociallymonogamous species.     

Female extrapair mate choice in a cooperative breeder: trading sex for help and increasing offspring heterozygosity

Sexual conflict between males and females over mating is common. Females that copulate with extrapair mates outside the pair-bond may gain (i) direct benefits such as resources or increased paternal care, (ii) indirect genetic benefits for their offspring, or (iii) insurance against infertility in their own social mate. Few studies have been able to demonstrate the different contexts in which females receive varying types of benefits from extrapair mates. Here, I examined sexual conflict, female extrapair mate choice, and patterns of extrapair paternity in the cooperatively breeding superb starling Lamprotornis superbus using microsatellite markers. Although extrapair paternity was lower than many other avian cooperative breeders (14% of offspring and 25% of nests), females exhibited two distinct mating patterns: half of the extrapair fertilizations were with males from inside the group, whereas half were with males from outside the group. Females with few potential helpers copulated with extrapair mates from within their group and thereby gained direct benefits in the form of additional helpers at the nest, whereas females paired to mates that were relatively less heterozygous than themselves copulated with extrapair mates from outside the group and thereby gained indirect genetic benefits in the form of increased offspring heterozygosity. Females did not appear to gain fertility insurance from copulating with extrapair mates. This is the first study to show that individuals from the same population mate with extrapair males and gain both direct and indirect benefits, but that they do so in different contexts.     

Male mating strategies and the mating system of great-tailed grackles

Great-tailed grackles (Quiscalus mexicanus) are sexually dimorphic,dichromatic, colonially nesting blackbirds. In this study, males pursued three basic types of conditional mating strategies,each of which employed a different set of mating tactics. Territorialmales defended one or more trees in which several females nested.They achieved reproductive success by siring the offspringof their social mates and through extrapair fertilization.Resident males lived in the colony but did not defend territoriesor have social mates. Transient males passed through the colony, staying no more than a few days, and probably visited more thanone colony. Residents appeared to queue for access to territories,but transients did not. Residents and transients gained allpaternity through extrapair fertilizations and provided noparental care. Territorial males sired the majority of offspring,but residents and transients also sired small numbers of nestlings. Territorial males were larger and had longer tails than nonterritorialmales. The number of social mates was related to body size,and males that sired nestlings were heavier and had longertails than males with no genetic reproductive success. Malesthat gained paternity through extrapair fertilization wereheavier and had longer tails than males that did not. The matingsystem of great-tailed grackles can best be categorized as "non-faithful-female frank polygyny."     

Are there correlates of male Australian Magpie Gymnorhina tibicen reproductive success in a population with high rates of extra‐group paternity?

The reproductive success of a male bird is often correlated with measurable traits that predict his intrinsic quality. Females are thought to base their selection of mates on the latter's 'quality' in order to gain their 'good genes'. Male Australian Magpies Gymnorhina tibicen of the white-backed race tyrannica were trapped in two breeding seasons. Measurements were taken of morphometric and other characteristics in order to discover whether particular traits of males were associated with: (1) percentage of offspring sired in the territory, (2) number of fledglings produced in the territory per season and (3) whether females select males for their 'good genes'. There were no consistently significant correlations between any of the measured variables and male Magpie reproductive success within territories. In particular, none of the traits measured had any consistent correlation with the percentage of offspring sired in a territorial group. This was an unexpected result given that the species is strongly territorial but also engages regularly in extra-group copulations. These findings appear contrary to the predictions of the 'good genes' hypothesis. The general lack of correlation between the variables and level of genetic paternity may in fact be due to females engaging in extra-group mating primarily to avoid breeding with a close relative rather than to choose a high-quality male. In this case, males would not have to be 'high quality', but merely genetically different from the female's social mate.     

Dirty ptarmigan: behavioral modification of conspicuous male plumage

Males of many bird species acquire a conspicuous breeding plumagethrough molt. Male rock ptarmigan (Lagopus mutus), however,become conspicuous in a unique way—as snow melts awayfrom the tundra, their cryptic white winter plumage suddenlybecomes exceptionally conspicuous, and remains so for at least3 weeks. While males remain white, females molt into one ofthe most cryptic plumages known in birds. From our 17-year fieldstudy in arctic North America, we show that, unlike other birds,male rock ptarmigan eventually change from conspicuous to crypticby soiling their plumage, thereby reducing their conspicuousnesssix fold before they molt to their cryptic summer plumage.Individual males began to soil their plumage as soon as theirmates began egg-laying, and were maximally dirty and relatively cryptic by the time incubation began and their mates no longerfertilizable. Thus male plumage conspicuousness appears toserve a reproductive function. Moreover, both polygynous andbachelor males delayed soiling for a few days after monogamousmales, as expected because of the prolonged mating opportunitiesavailable to them. We use these data to address a variety of hypotheses to explain both the conspicuousness of breeding malesand their subsequent plumage soiling. Given the high predationrate recorded for male ptarmigan during the breeding season,we argue that male conspicuousness is best explained by sexualselection and that plumage soiling is an adaptation that reducespredation risk by increasing camouflage.     

Ecological, social, and genetic contingency of extrapair behavior in a socially monogamous bird

Extrapair mating strategies are common among socially monogamous birds, but vary widely across ecological and social contexts in which breeding occurs. This variation is thought to reflect a compromise between the direct costs of mates' extrapair behavior and indirect benefits of extrapair fertilizations (EPF) to offspring fitness. However, in most free-living populations, the complete spatial and temporal distribution of mating attempts, genetic characteristics of available mates, and their relative contribution to EPF strategies are difficult to assess. Here we examined prevalence of EPF in relation to breeding density, synchrony, and genetic variability of available mates in a wild population of house finches Carpodacus mexicanus where all breeding attempts are known and all offspring are genotyped. We found that 15% of 59 nests contained extra-pair offspring and 9% of 212 offspring were sired by extra-pair males. We show experimentally that paired males and females avoided EPF displays in the presence of their social partners, revealing direct selection against EPF behavior. However, at the population level, the occurrence of EPF did not vary with nests dispersion, initiation date, synchrony, or with distance between the nests of extrapair partners. Instead, the occurrence of EPF closely covaried with genetic relatedness of a pool of available mates and offspring of genetically dissimilar mating tended to be resistant to a novel pathogen. These results corroborate findings that, in this population, strong fitness benefits of EPF are specific to each individual, thus highlighting the ecological, social, and genetic contingency of costs and benefits of an individual's extrapair behaviors.     

Ecological correlates of extra-group paternity in mammals

Extra-group paternity (EGP) can form an important part of the mating system in birds and mammals. However, our present understanding of its extent and ecology comes primarily from birds. Here, we use data from 26 species and phylogenetic comparative methods to explore interspecific variation in EGP in mammals and test prominent ecological hypotheses for this variation. We found extensive EGP (46% of species showed more than 20% EGP), indicating that EGP is likely to play an important role in the mating system and the dynamics of sexual selection in mammals. Variation in EGP was most closely correlated with the length of the mating season. As the length of the mating season increased, EGP declined, suggesting that it is increasingly difficult for males to monopolize their social mates when mating seasons are short and overlap among females in oestrus is likely to be high. EGP was secondarily correlated with the number of females in a breeding group, consistent with the idea that as female clustering increases, males are less able to monopolize individual females. Finally, EGP was not related to social mating system, suggesting that the opportunities for the extra-group fertilizations and the payoffs involved do not consistently vary with social mating system.     

Experimental evidence that brighter males sire more extra‐pair young in tree swallows

Across taxa, extra‐pair mating is widespread among socially monogamous species, but few studies have identified male ornamental traits associated with extra‐pair mating success, and even fewer studies have experimentally manipulated male traits to determine whether they are related directly to paternity. As a consequence, there is little experimental evidence to support the widespread hypothesis that females choose more ornamented males as extra‐pair mates. Here, we conducted an experimental study of the relationship between male plumage colour and fertilization success in tree swallows (Tachycineta bicolor), which have one of the highest levels of extra‐pair mating in birds. In this study, we experimentally dulled the bright blue plumage on the back of males (with nontoxic ink markers) early in the breeding season prior to most mating. Compared with control males, dulled males sired fewer extra‐pair young, and, as a result, fewer young overall. Among untreated males, brighter blue males also sired more extra‐pair young, and in paired comparisons, extra‐pair sires had brighter blue plumage than the within‐pair male they cuckolded. These results, together with previous work on tree swallows, suggest that extra‐pair mating behaviour is driven by benefits to both males and females.     

Condition-dependent genetic benefits of extrapair fertilization in female blue tits Cyanistes caeruleus

In many socially monogamous birds, both partners perform extrapair copulations (EPC). As this behaviour potentially inflicts direct costs on females, they are currently hypothesized to search for genetic benefits for descendants, either as 'good' or 'complementary' genes. Although these hypotheses have found some support, several studies failed to find any beneficial consequence of EPC, and whether this behaviour is adaptive to females is subject to discussion. Here, we test these two hypotheses in a natural population of blue tits by accounting for the effect of most parameters known to potentially affect extrapair fertilization. Results suggest that female body mass affected the type of extrapair genetic benefits obtained. Heavy females obtained extrapair fertilizations when their social male was of low quality (as reflected by sexual display) and produced larger extrapair than within-pair chicks. Lean females obtained extrapair fertilizations when their social mate was genetically similar, thereby producing more heterozygous extrapair chicks. Our results suggest that mating patterns may be condition-dependent.     

The social organization of the Scarlet Robin Petroica multicolor and Flame Robin P. phoenicea in southeastern Australia: a comparison between sedentary and migratory flycatchers

Scarlet Robins Petroica multicolor and Flame Robins P. phoenicea occurred sympatrically during the breeding season in southeastern Australia. Scarlet Robins that occur territories in forest habitat remained there throughout the year, while those, mostly first-year birds, that occupied territories in grassland habitat were present only during the non-breeding season. Flame Robins were present for 9 months of the year and were territorial for 6 of those months. The migratory Flame Robin did not show more intense or prolonged territorial or courtship behaviour than the sedentary Scarlet Robin, despite having to obtain territories and mates when it returned each year. It is suggested that the similarities between the two species' social organizations arise partly from high adult survivorship (70–75%) and lengthy breeding seasons (4–5 months). High adult survivorship and scarcity of suitable breeding habitat also caused intense competition for territories and mates, and appears to have led to the evolution of bright, signalling plumages among female and young male Scarlet Robins. Scarcity of females and breeding habitat may have caused delayed maturation of plumage among male Flame Robins.     

Part-Time Mate Guarding Affects Paternity in Male Reed Buntings (Emberiza schoeniclus)

Male mate guarding by close following has been reported in many socially monogamous bird species and is generally believed to function as a paternity guard. Many aspects of the dynamics and effectiveness of this behavior are still however poorly understood. Here, we describe the temporal variation in mate guarding behavior in male reed buntings (Emberiza schoeniclus) with a particular focus on how males allocate their mating effort between mate guarding and extrapair mating in a context of intense sperm competition. In our highly synchronous study population most males have to balance the simultaneous and mutually exclusive demands of mate guarding and seeking extrapair copulations (EPCs). We found that males frequently switched between guarding their mates and performing intrusions to neighboring territories. Both activities seemed to have significant fitness payoffs, as male mate guarding effort had a positive effect on paternity, and a large fraction of extrapair fertilizations occurred during the days when the sire guarded its own female. The reed bunting is thus an example of how discontinuous or part‐time mate guarding can still be effective in securing paternity. Female reed buntings were not particularly active in initiating EPCs as they never were observed performing extraterritorial forays. We argue that the absence of female‐initiated EPCs is a prerequisite for males to trade mate guarding against seeking EPCs. Otherwise, if females circumvent male mate guarding by timing their EPCs to periods of male absence, males should guard their mates almost continuously or rely on alternative paternity guards.     

Late breeding season definitive prebasic molt in males,and late breeding season brood care by females,in central California Wilson’s warblers

I made observations of a central California population of Wilson''s Warbler, Cardellina pusilla, after July 1 over 10 breeding seasons. I sighted males in definitive prebasic molt from July 4 (in 2007) to September 1 (in 1999). Most territorial males molted on their breeding territories, and individual molt lasted up to 46 days. Following prebasic molt, territorial males engaged in subdued “post‐molt singing,” which lasted about 7 days in some males, and which I first heard on August 13 (in 2004) and last heard on September 6 (in 1999). I sighted no female in definitive prebasic molt, or in fresh basic plumage, during the study. Of 13 females sighted ≥ July 21, 11 were in late breeding season uniparental brood care, and I could not rule out late brood care for the other two. Most, and possibly all, females not engaged in late season uniparental brood care apparently vacated their breeding territories before July 21. This departure was much earlier than for resident males, the last of which I sighted on September 10 (in 1999). Early‐departing females presumably underwent prebasic molt after July 21 at locations not known. Remaining late‐nesting females must have molted much later than resident males and likely later than early‐departing females, and at locations unknown. I last sighted two uniparental brood‐tending females, still in worn plumage, on August 26 and 29, respectively. Two unique findings of this study are a male/female difference in location of prebasic molt, and a likely dichotomy of prebasic molt timing between females leaving their breeding territories early and those remaining in uniparental brood care. Another finding, post‐molt singing in most and possible all territorial males, is a largely unrecognized behavior, but one previously reported in several passerine species. Post‐molt singing may reliably indicate completion of prebasic molt.     

Microsatellite identification of extrapair sires in a socially monogamous warbler

Few studies of avian mating systems have identified the siresof extrapair young, and hence it has been difficult to determinethe scale at which reproductive interactions occur. For instance,females may be free to copulate with any male in the population(a "global" scale of interactions), or females may be restrictedto copulating only with males on neighboring territories (a"local" scale). The scale of such interactions has importantconsequences for an understanding of the evolutionary causesand consequences of extrapair fertilizations. We used five hypervariable microsatellite loci and multilocus DNA fingerprintingto examine parentage of more than 400 nestling black-throatedblue warblers (Dendroica caerulescens). Extrapair fertilizationswere common, and the microsatellite markers allowed us to identifythe sires for 89% of the young analyzed. Most identified extrapairsires were males on neighboring or nearby territories, andmost nestlings for whom we could not identify a sire came fromterritories at the edge of the study plot. Thus, reproductive interactions appear to be more local than global in this population.Extrapair fertilizations contributed significantly to totalvariation in male reproductive success. However, the standardizedvariance in male reproductive success (0.68-0.74) was not substantiallygreater than that for females (0.53-0.60), and the contributionof extrapair fertilizations (9-14%) was much lower than thecontribution of within-pair fertilizations (75-77%). This suggeststhat the local scale of reproductive interactions may limitvariation in male reproductive success and hence the opportunityfor selection.     

Plumage redness predicts breeding onset and reproductive success in the House Finch: a validation of Darwin's theory

Darwin (1871) and later Fisher (1958) suggested that sexual selection can drive the evolution of ornamental traits in monogamous species when female preferences for these traits allow well-ornamented males to begin breeding earlier in a season and, as a result, gain reproductive advantages over poorly ornamented males. However, few studies have been conducted to test this fundamental concept upon which much of the sexual selection theory for monogamous species has been based. In this study, we examined the relationship between breeding onset, reproductive success, and male ornamentation in the House Finch Carpodacus mexicanus , a species in which males display bright carotenoid-based plumage pigmentation. In previous work, it has been shown that bright male House Finches are preferred as social mates by females and, as a result, begin nesting earlier in the season than do drab orange and yellow males. Here we show that, by initiating breeding earlier in the season, brightly colored males fledge more offspring in a season than do drab males. Thus, differential timing of breeding generates considerable variance in reproductive success among male House Finches and contributes to sexual selection for male plumage ornamentation in this species.     

Male brood provisioning rates provide evidence for inter‐age competition for mates in female Cooper's Hawks Accipiter cooperii

Life history theory predicts that individuals should maximize lifetime reproductive success (LRS) by breeding as soon as they reach sexual maturity, yet many species delay breeding, either because there are insufficient available mates or breeding sites, or because delayed breeding yields higher LRS. Accipitriform species, such as Cooper's Hawk Accipiter cooperii, exhibit both delayed breeding and delayed plumage maturation. However, in certain circumstances, first‐year females in non‐definitive plumage do breed and apparently compete with older females for high‐quality breeding territories. We predicted that these young females are at a competitive disadvantage compared with older females and that older females would have both higher reproductive success and be able to acquire higher quality nesting territories. We conducted brood counts and measured prey delivery rates by male Cooper's Hawks in an expanding urban population located in Albuquerque, New Mexico (USA), to assess our prediction. We found that older females had higher reproductive success, fledging 1.6 more offspring than younger females, and that they occupied territories where males provisioned at higher rates of 0.37 more prey items per 2‐h period. Our results showed that older females fared better than first‐year females but it is unclear if this is the result of passive or active competition. Older females initiated nesting 14.3 days sooner than first‐year females and thus may have filled vacant, high‐quality territories before first‐year females began seeking mates. Additionally, first‐year females were never observed persistently to confront older females for breeding territories, but they did actively compete against each other. First‐year females may defer to older females who, in a direct competitive interaction, would be most likely to prevail. Thus, delayed plumage maturation in Cooper's Hawks may serve to focus competition for nesting territories within age classes.     

Genetic similarity, extrapair paternity, and offspring quality in Savannah sparrows (Passerculus sandwichensis)

The occurrence of extrapair paternity (EPP) in birds is oftenattributed to the action of good-genes sexual selection wherebyfemales "trade up" on male genetic quality by allocating fertilizationsto males with better genes than those possessed by their socialmate. To date, most studies of EPP in birds focus on absolutemeasures of male quality as a criterion for female choice, althoughmultiple mating by females in other taxa is more commonly ascribedto benefits associated with the individual optimization of offspringgenotypes. Here, we examine whether the genetic similarity ofsocial mates predicts female mating patterns in a populationof Savannah sparrows (Passerculus sandwichensis) where as manyas 70% of adults produce extrapair young (EPY). We considerthe influence of genetic similarity across all stages of a female'sdecision-making process, from pair formation through the decisionto produce EPY, to the allocation of fertilizations to specificextrapair sires. In a 4-year study of 175 males, 206 females,and 506 offspring, females were more likely to produce EPY whenpaired to genetically similar males, but they did not appearto be influenced by the size, age, mass, individual heterozygosity,and genetic diversity of their social mates. In paired comparisons,females were almost twice as likely to decrease their geneticsimilarity to males when producing EPY as they were to increaseit. Nonetheless, females did not select especially dissimilarmales when mating outside the pair-bond nor did they pair disassortativelywith respect to genetic similarity. Relative measures of malequality may influence mating patterns in birds, but only atsome points in a female's decision-making process.