Breeding rate is associated with pheomelanism in male and with eumelanism in female barn owls

Melanin-based coloration exists in 2 types: black eumelanismand reddish-brown pheomelanism, which both have a strong heritablecomponent. To test whether these 2 types of melanism are associatedwith alternative adaptations, we carried out a correlative studyover 8 years and an experiment in a Swiss population of barnowls, Tyto alba. This species varies in coloration from reddish-brownto white and from lightly to heavily marked with black spots.Based on the fact that plumage coloration and spottiness aremale- and female-specific secondary sexual characters, respectively,we examined whether the probability of breeding is associatedwith the degree of pheomelanism in males and of eumelanism infemales. In males, recruited nestlings were significantly lessreddish-brown than their nonrecruited nest mates. In females,individuals displaying larger black spots started to breed ata younger age and had a higher survival, and females with experimentallyreduced plumage spottiness bred less often than control females.Therefore, in the barn owl, the degree of male pheomelanismis associated with the probability of being recruited in thelocal population, whereas the degree of female eumelanism correlateswith age at sexual maturity, survival probability, and alsothe probability of skipping reproduction.     

Nonrandom pairing by male barn owls (Tyto alba) with respect to a female plumage trait

In socially monogamous species it is rare for females to bemore intensely colored than males. The barn owl (Tyto alba)is one of the exceptions, as females usually exhibit more andlarger black spots on the plumage. The evolution of sexual dimorphismin plumage traits is commonly assumed to be the result of sexualselection. I therefore examined the prediction that male barnowls do not pair randomly with respect to female plumage spottinessduring a 5-year study in Switzerland. The prediction was supported,as males that changed mates acquired a new female that was similarlyspotted to the previous one, and pairing with respect to plumage spottinesswas positively assortative. Significant repeatability in male pairingwas presumably neither the consequence of sharing the same habitats withfemales displaying a given plumage spottiness nor of morphological characteristicsof the males that could influence mate sampling. A resemblance inplumage spottiness between the mates of sons and of their fathersuggests that repeatability could have resulted from sexualimprinting and/or heritable variance in male preference forspotted females. To test whether males assess female plumagespottiness, I either cut off black spots or small pieces of feathersbut not the spots of already mated females. Males mated to females withreduced plumage spottiness fed their brood at a lower cadencyand achieved a lower reproductive success than other males.This experiment further suggests that female plumage spottinessis a stimulus for males.     

Female plumage spottiness signals parasite resistance in the barn owl (Tyto alba)

The hypothesis that extravagant ornaments signal parasite resistancehas received support in several species for ornamented malesbut more rarely for ornamented females. However, recent theorieshave proposed that females should often be under sexual selection,and therefore females may signal the heritable capacity toresist parasites. We investigated this hypothesis in the sociallymonogamous barn owl, Tyto alba, in which females exhibit on average more and larger black spots on the plumage than males,and in which males were suggested to choose a mate with respectto female plumage spottiness. We hypothesized that the proportionof the plumage surface covered by black spots signals parasiteresistance. In line with this hypothesis, we found that theectoparasitic fly, Carnus hemapterus, was less abundant onyoung raised by more heavily spotted females and those flieswere less fecund. In an experiment, where entire clutches werecross-fostered between nests, we found that the fecundity ofthe flies collected on nestlings was negatively correlatedwith the genetic mother's plumage spottiness. These resultssuggest that the ability to resist parasites covaries with theextent of female plumage spottiness. Among females collecteddead along roads, those with a lot of black spots had a smallbursa of Fabricius. Given that parasites trigger the developmentof this immune organ, this observation further suggests thatmore spotted females are usually less parasitized. The same analyses performed on male plumage spottiness all provided non-significant results. To our knowledge, this study is the first one showingthat a heritable secondary sexual characteristics displayedby females reflects parasite resistance.     

Achromatic plumage reflectance predicts reproductive success in male black-capped chickadees

The size of achromatic (black, white, gray) plumage patchesserves as a male status signal in many species of birds, butvariation in the colors of these patches has received littleattention. We assessed the relation between achromatic plumagereflectance, dominance rank, body condition, and reproductivesuccess in male black-capped chickadees, Poecile atricapillus.We measured plumage reflectance for five body regions of 40male chickadees in late winter and monitored these males throughoutthe following breeding season to determine whether they survivedto breed, whether they successfully paired, whether their partnerlaid eggs, and both their apparent and realized reproductivesuccess. As expected from past studies, a male's dominance ranksignificantly predicted whether his partner laid eggs. However,only achromatic plumage reflectance significantly predictedother measures of male reproductive performance. Among maleswho fledged at least one offspring, both the brightness of whiteplumage regions and the UV-chroma of melanin-based plumage regionswere significant predictors of the proportion of within-pairyoung in their nests. When we consider all males we measured,assigning zero values to males who failed to sire any offspring,the UV-chroma of melanin-based plumage regions was a significantpredictor of realized reproductive success. Bib size was alsorelated to male realized reproductive success. Our findingssuggest that individual variation in achromatic plumage mayplay an important role in sexual signaling in chickadees.     

Plumage phenotypes and mating preferences in Japanese quail

A series of trials was conducted to study the relationship of plumage phenotype with choice of mate. Males which exhibited preferences tended to choose either females of their own kind, those of a plumage color with which they had prior experience, or those of the darker hue in a choice situation.Wild-type males which had no prior experience with albino females, tended to avoid albinos in preference to wild-type hens. This preference persisted when the head and neck plumage of albinos was dyed black, but when the body plumage of the albinos was dyed black, wild-type males did not exhibit a preference between them and wild-type females. The data suggest that body plumage color is a factor in the male choice of females.     

Concordant evolution of plumage colour, feather microstructure and a melanocortin receptor gene between mainland and island populations of a fairy-wren

Studies of the patterns of diversification of birds on islands have contributed a great deal to the development of evolutionary theory. In white-winged fairy-wrens, Malurus leucopterus, mainland males develop a striking blue nuptial plumage whereas those on nearby islands develop black nuptial plumage. We explore the proximate basis for this divergence by combining microstructural feather analysis with an investigation of genetic variation at the melanocortin-1 receptor locus (MC1R). Fourier analysis revealed that the medullary keratin matrix (spongy layer) of the feather barbs of blue males was ordered at the appropriate nanoscale to produce the observed blue colour by coherent light scattering. Surprisingly, the feather barbs of black males also contained a spongy layer that could produce a similar blue colour. However, black males had more melanin in their barbs than blue males, and this melanin may effectively mask any structural colour produced by the spongy layer. Moreover, the presence of this spongy layer suggests that black island males evolved from a blue-plumaged ancestor. We also document concordant patterns of variation at the MC1R locus, as five amino acid substitutions were perfectly associated with the divergent blue and black plumage phenotypes. Thus, with the possible involvement of a melanocortin receptor locus, increased melanin density may mask the blue-producing microstructure in black island males, resulting in the divergence of plumage coloration between mainland and island white-winged fairy-wrens. Such mechanisms may also be responsible for plumage colour diversity across broader geographical and evolutionary scales.     

Structural coloration and sexual selection in the barn swallow Hirundo rustica

Structural coloration has been hypothesized to play a role insexual selection, and we tested whether this was the case ina field study of the barn swallow Hirundo rustica. The dorsaliridescent plumage of barn swallows has a strong reflectancein the ultraviolet (UV) region, with adult males on averagereflecting 8-9% more than adult females, as revealed by a 2-yearstudy in southwestern Spain. The correlation between structural coloration (described by the reflectance in the UV part of thespectrum, UV chroma and blue chroma) and three other secondarysexual characters significantly associated with male matingsuccess (tail length, tail asymmetry, and red facial coloration)was weak and generally nonsignificant. Nor was there a significantrelationship between color parameters and body condition. Wetested for an association between structural coloration of the dorsal plumage and sexual selection in a number of independenttests. Arrival date of males was not significantly relatedto color; there was no significant relationship between colorationand probability of survival or age; mated males did not havestronger reflectance than unmated males; and the duration ofthe premating period was not significantly related to color.Reproductive success was not significantly correlated withplumage coloration in males, nor was the feeding rate of offspringby brightly colored males higher than that of males with lessbright plumage. Given that sample sizes were large, and the power of statistical tests high, we conclude that current sexualselection on the coloration of the dorsal plumage in the barnswallow is, at best, weak.     

Sexually selected male plumage color is testosterone dependent in a tropical passerine bird, the red-backed fairy-wren (Malurus melanocephalus)

Background

Sexual signals, such as bright plumage coloration in passerine birds, reflect individual quality, and testosterone (T) may play a critical role in maintaining signal honesty. Manipulations of T during molt have yielded mixed effects on passerine plumage color, in most cases delaying molt or leading to production of drab plumage. However, the majority of these studies have been conducted on species that undergo a post-nuptial molt when T is low; the role of T in species that acquire breeding plumage during a pre-nuptial molt remains largely unexplored.

Methodology/Principal Findings

We experimentally tested the effects of increased T on plumage color in second-year male red-backed fairy-wrens (Malurus melanocephalus), a species in which after-second-year males undergo a pre-nuptial molt into red/black (carotenoid and melanin-based) plumage and second-year males either assume red/black or brown breeding plumage. T treatment stimulated a rapid and early onset pre-nuptial molt and resulted in red/black plumage acquisition, bill darkening, and growth of the sperm storage organ, but had no effect on body condition or corticosterone concentrations. Control males molted later and assumed brown plumage. T treated males produced feathers with similar but not identical reflectance parameters to those of unmanipulated after-second-year red/black males; while reflectance spectra of red back and black crown feathers were similar, black breast feathers differed in UV chroma, hue and brightness, indicating a potentially age and plumage patch-dependent response to T for melanin- vs. carotenoid-pigmentation.

Conclusions/Significance

We show that testosterone is the primary mechanism functioning during the pre-nuptial molt to regulate intrasexually variable plumage color and breeding phenotype in male red-backed fairy-wrens. Our results suggest that the effects of T on plumage coloration may vary with timing of molt (pre- vs. post-nuptial), and that the role of T in mediating plumage signal production may differ across age classes, plumage patches, and between pigment-types.     

Mate Choice in Experimentally Parasitized Rock Doves: Lousy Males Lose

A recent model by Hamilton and Zuk (1982) suggests that exaggeratedsecondary sexual traits facilitate mate choice for genetic resistanceto parasites. The model predicts that individuals discriminateagainst parasitized mates by scrutinizing traits indicativeof parasite load. In the case of birds and their feather-feedinglice, for example, individuals might avoid parasitized matesbydetecting reduced plumage brightness, reduced courtship display,or increased grooming. I conducted a series of mate choice trialsin which female Rock Doves (Columba livia) were allowed to choosebetween "clean" males without lice and "lousy" males with experimentallyincreased loads. Clean males displayed significantly more oftenthan lousy males and females demonstrated a significant preferencefor clean males. Lousy males were subject to plumage damage;however, none of the damage was externally visible, and thetime spent grooming by clean and lousy males did not differsignificantly. Female louse loads, which were also manipulated,were not significantly related to female mating preferences.These results are consistent with the Hamilton-Zuk model. Theyare also consistent with a model of sexual selection for theavoidance of parasite transmission, which is discussed. Thegeneral relevance of lice and other ectoparasites to modelsof parasite-mediated sexual selection is reviewed.     

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.     

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.     

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.     

黄腹山鹪莺稳定的配偶关系限制雄性欺骗者

多数鸟类通过性特征限制在同性竞争和配偶选择中的“欺骗者”存在,与此相反,雀形目扇尾莺科部分物种表现出繁殖季节性特征消退的身体特征变化模式.在广州市南沙区通过“目字笼”对黄腹山鹪莺配偶关系稳定性的限制机制进行研究,发现虽然雌性个体到访原配个体和对照个体的次数几乎相同,但是雌性个体对原配雄性的单次选择时间明显长于对照雄性个体,总计选择时间也明显长于对照雄性个体.选择实验过程中,原配雄性的跳动次数明显高于对照个体雄性,以竖尾扑哧和鸣声恐吓等为代表的威慑行为次数也明显高于对照雄性个体.结果说明,雌性更青睐于原配个体,配对时间越长,忠诚度越高,而且原配雄性比入侵雄性个体表现出更高的活跃度和威慑行为.繁殖季节性特征消退的物种可以通过保持稳定的配偶关系以限制“欺骗者”存在.可以推测繁殖的巨大投入和雌性之间的同性竞争可能是产生这种配偶稳定性的主要原因.     

Costs and Benefits of Subadult Plumage in Mute Swans: Testing Hypotheses for the Evolution of Delayed Plumage Maturation

In some avian species, young birds capable of reproducing diminish their prospects of doing so by molting into a subadult plumage that accurately signals their subadult status. Several hypotheses have been proposed to explain the evolution of delayed plumage maturation, but testing them usually has involved interspecific comparisons that are hard to interpret. Mute swans (Cygnus olor) exhibit two phenotypes that differ in whether the birds have a gray subadult plumage (SAP phenotype) or molt immediately into an all white adult plumage (AP phenotype). The AP phenotype results from a recessive allele on the X chromosome; both phenotypes occur in the same population and even in the same brood. We compared costs and benefits of both phenotypes in mute swans on the Chesapeake Bay in 1972-1980 and on Long Island Sound in 1982-1989. Swans with the SAP phenotype had higher survival rates from hatching to fledging than AP swans. In the fall, when AP cygnets began to molt into their white plumage, their parents often attacked and drove them off while allowing SAP cygnets from the same brood to remain on their territories for several more months. SAP males had higher survival rates during their first 2 yr of life than AP males, but AP swans bred at a younger age than SAP swans. The only proposed hypothesis for the evolution of delayed plumage maturation that can explain its occurrence in mute swans is the status-signaling hypothesis. This hypothesis argues that males with subadult plumage honestly advertise their age and subordinate status while AP swans are cheaters and engaging in dishonest communication. SAP males acquire a longer period of parental care, suffer less aggression from older birds, and increase their survival but forgo the opportunity to breed at an early age. This is a unique example of how a single gene resulted in either honest or dishonest communication, changed a bird's relationship with its parents and potential mates, and altered the bird's chances to survive and to reproduce.     

Dietary mineral content influences the expression of melanin-based ornamental coloration

Many animals develop bold patches of black or brown colorationthat are derived from melanin pigments and serve as sexual orsocial signals. At present, there is much debate among behavioralecologists over whether melanin-based color signals are costlyto produce. Studies that have manipulated crude aspects of nutrition(i.e., total food intake) or health have generally found melanin-basedplumage ornaments to be less responsive to such factors thanother types of extravagant color (e.g., carotenoid or structuralbased). However, a recently advanced hypothesis argues thatlimited minerals in the diet, such as calcium (Ca), zinc (Zn),and iron (Fe), may serve to increase melanin pigment productionand maintain signal honesty. Here, I experimentally tested whethervariation in the calcium content of the diet affects the colorand extent of melanin-based plumage in male zebra finches (Taeniopygiaguttata). Calcium supplementation increased the size, but notdarkness, of the black breast plumage patch in fledgling andadult males; however, sexually selected, carotenoid-based redbeak coloration was not affected by the diet manipulation. Theseresults are the first to support the idea that acquisition ofminerals from the diet is a unique, limiting factor for theexpression of ornamental melanin coloration in animals.     

Timing of breeding and offspring number covary with plumage colour among Gyrfalcons Falco rusticolus

Plumage colour variation exists among Gyrfalcons throughout their Arctic and sub‐Arctic circumpolar distribution, ranging from white through silver and grey to almost black. Although different colour variants coexist within many populations, a few geographical regions, such as northern Greenland, possess a single variant, suggesting that local environments may influence plumage colour variation. In central‐west Greenland (66.5–67.5°N), where multiple colour variants exist, white male Gyrfalcons fathered significantly earlier clutches than grey males. No significant association was observed between female colour and lay date. However, significantly more offspring were produced by both male and female white Gyrfalcons than by grey variants when controlling for lay date, and silver Gyrfalcons produced an intermediate number of offspring for both sexes. This pattern was further supported by breeding plumage colour pairings. Grey females paired with grey males nested significantly later in the season and produced fewer offspring than those paired with white males, whereas no difference in lay date or offspring number was found between white males paired with white or with grey females. The difference in the number of offspring produced at each nest‐site was also inversely correlated with the distance to the nearest neighbouring nest, and grey males nested in closer proximity to other nests compared with white and silver colour variants. These results suggest that factors associated with territory occupancy and timing of breeding may regulate reproductive success differently between colour variants, with directional selection favouring light‐coloured Gyrfalcons and resulting in earlier lay date and a high frequency of white plumage colour variants in this population. Although gene flow exists between our study population and those further north (>75°N), white Gyrfalcons prevail where the breeding season duration is even shorter, suggesting that nesting chronology in combination with genetic drift may play an important role in influencing plumage colour polymorphism among Gyrfalcon populations.     

Testosterone treatment is immunosuppressive in superb fairy-wrens, yet free-living males with high testosterone are more immunocompetent

The immunocompetence handicap hypothesis proposes that the immunosuppressive effect of testosterone enforces honesty of sexual signalling via a physiological trade-off between signal intensity and immunocompetence. However, evidence that testosterone is immunosuppressive is scant, particularly in birds. I studied the correlation between immunocompetence and testosterone in superb fairy-wrens (Malurus cyaneus), a species with intense intersexual selection. Males are seasonally dichromatic and testosterone increases during the moult from dull brown eclipse plumage into bright nuptial plumage. I determined the primary antibody response to immunization with sheep red blood cells (SRBCs) in (i) control and testosterone-implanted males in captivity, and (ii) a cross-section of free-living males with basal and elevated testosterone (in eclipse plumage, moulting and in nuptial plumage). Experimental treatment with testosterone decreased the likelihood of an antibody response to SRBCs in captive birds. In contrast, free-living males which had acquired the nuptial plumage and had naturally elevated testosterone were more likely to respond to SRBCs than males in eclipse plumage with basal testosterone levels. The association between higher immunocompetence and higher immunosuppressive testosterone could arise if both are positively correlated with male phenotypic quality In addition, the association could result if males compensate for potential immunosuppression by enhancing their humoral immune responses, particularly since high testosterone is linked to other demanding activities such as moulting and courtship displays.     

Dietary carotenoid pigments and immune function in a songbird with extensive carotenoid-based plumage coloration

Carotenoid pigments can directly enhance the immune responsesof vertebrates, and they are used by many animals to createornamental color displays. It has been hypothesized that thesetwo functions of carotenoid pigments are linked: animals musttrade off use of carotenoid pigments for immune function versusornamental display. We tested two key predictions of this hypothesiswith captive American goldfinches, Carduelis tristis, a specieswith extensive carotenoid-based plumage coloration. First, wetested whether the immune systems of male goldfinches are carotenoidlimited during molt by supplying treatment groups with low,approximately normal, or high dietary access to lutein and zeaxanthin.Dietary treatment had a significant effect on plumage and billcolor but not on immunocompetence. We compared the cell-mediatedand humoral immune responses and the course of disease afterinfection for males in the different treatments. We observedno significant effect of the carotenoid content of diet on immuneresponse or disease resistance. Second, we tested whether therewas a positive relationship between immune function and expressionof ornamental coloration by comparing both the pre- and posttreatmentplumage coloration of males to their immune responses. We failedto find the predicted trade-off between ornament display andimmune function. These findings do not support the hypothesisthat songbirds with extensive carotenoid-based plumage displaystrade off the use of carotenoids for ornamentation versus immunefunction.     

Assortative mating by multiple ornaments in northern cardinals (Cardinalis cardinalis)

In positive assortative mating, individuals of similar phenotypemate together more frequently than expected by chance. Assortativemating by a variety of qualities, including ornamentation, iswell documented in birds. Studies of assortative mating by ornamentshave focused on single, highly conspicuous ornaments, but manyspecies of birds possess multiple ornaments in both sexes. Wecompared ornament expressions between mates of northern cardinals(Cardinalis cardinalis) to determine if assortative mating occurredby one or more of the four ornaments displayed by both sexes.All cardinals possess tall head crests and red-orange bills.In addition, males have black face masks and entirely red bodyplumage, whereas females have blackish face masks and red underwingcoverts. We predicted that cardinals mate assortatively by plumagecolor because red plumage expression has been shown to indicatequality in both sexes. We found that cardinals mate assortativelyby plumage and bill color, the two ornaments colored by carotenoidpigments, but not by mask expression or crest length. Whetherthis mating pattern arises by mutual mate choice or intrasexualselection is not known.     

Effects of nestling condition on UV plumage traits in blue tits: an experimental approach

Intraspecific sexual and social communications are among themost important factors shaping costly color traits in birds.Condition capture models assume that only animals in superiorcondition can develop and maintain a colorful plumage. Althoughthere is good evidence that carotenoid-based components of plumagecolors show condition dependence, the situation is more controversialwith the underlying UV-reflecting structural component. We conducteda brood size manipulation in blue tits (Parus caeruleus) toinvestigate condition-dependent effects on plumage colorationin male and female offspring. Carotenoid chroma and UV reflectanceof the yellow breast plumage showed condition-dependent expressionin male and female fledglings. However, only males that wereraised in reduced broods had higher UV reflectance in the UV/bluetail feathers, whereas female tail coloration did not differbetween treatments. Our data suggest that there is a sex-specificeffect on the blue but not the yellow plumage and that thisis related to differences in the signaling function of bothplumage traits. Although sexual selection may already act onmale nestlings to develop colorful tail feathers for the nextbreeding season, the UV/yellow breast feathers are molted duringthe postjuvenile molt, and their signaling value is likely tobe important for both sexes during the extended postfledglingphase.