Plumage Ornaments Research Articles

Male’s age and plumage coloration predicts brood sex ratio in the Common Kingfisher (Alcedo atthis)

Plumage ornaments of birds, both pigment-based and structural, are considered age or condition-dependent, honestly signalling male quality, sexually selected traits, influencing the variation in breeding performance as well as adaptive sex allocation. In the present study, we examine the effect of age of males on the plumage structural colour in Common Kingfisher, and evaluate the breeding output (laying date, total number of young per breeding season, mean number of young per nest, total number of broods) and sex ratio in relation to two ornamental traits (forehead and rump structural colour). During the three years 2016–2018 in the Danube river system (south-western Slovakia), we collected data from 49 males, 102 broods and 645 nestlings. Our data demonstrate that structural colour is a condition-related and age-sensitive signal, while males with increased weight expressed less saturated blue forehead feathers, and old males displayed more saturated cyan rump feathers than young ones. Moreover, the brood sex ratio varies with male coloration in an age-dependent manner. The plumage colour of young males did not affect the brood sex ratio, whereas old males with increasing intensity of cyan rump had more sons than duller ones. Neither single ornamental trait nor age predicted breeding output of kingfisher males. Nevertheless, our results indicate that the blue structural plumage of kingfisher males may serve as an indicator of age and a certain kind of quality with a consequence on adaptive sex allocation in this species.

Coevolutionary maintenance of forked tails and song in hirundines (Aves: Hirundininae)

Both conspicuous plumage ornamentation and song are well‐known examples of sexually selected traits, but their interrelationship is not well known, perhaps in part because of confounding factors, including interspecific variation in ecology, habitat, morphology, and type of ornamentation. Here, using a phylogenetic comparative approach and the 69 species with available information (i.e. 96% of all 72 species), I examined the evolutionary relationship between forked tails and the presence/absence of song in hirundines (Aves: Hirundininae). Hirundines have similar ecology (e.g. aerial insectivores, social monogamy, and biparental provisioning), morphology (e.g. syrinx with nearly complete bronchial rings), and plumage ornamentation (i.e. a sexually selected forked tail), which provides a unique opportunity to examine the evolutionary associations between plumage ornamentation and song. In particular, hirundines have repeatedly lost their ornamentation, forked tails, setting up a condition to test their association with the evolutionary gain/loss of their simple song. After controlling for phylogeny and covariates, I demonstrated that song was less likely to be found in species with forkless tails than in species with forked tails. Two correlates of tail shape, sexual dimorphism in the overall plumage characteristics as a well‐known proxy of sexual selection and incubation type as a measure of extrapair mating opportunity, were not positively related to the presence or absence of song, indicating the importance of forked tails, rather than their correlates. The analysis of the correlated evolution of discrete characters further supported the correlated evolution of the two traits, in which forked tails and song are maintained together and less likely to be lost under the presence of each other. The current study provided macroevolutionary support for the integrated use of visual and acoustic courtship traits.

Social network positions of common waxbills are resilient to prolonged absence and to manipulation of ornamental plumage

Social network positions of common waxbills are resilient to prolonged absence and to manipulation of ornamental plumage

Song overlapping and matching during low‐arousal singing and their relation to visual ornaments, parental care and breeding success in the great tit (Parus major)

AbstractEavesdropping on interactions between conspecific animals provides a low‐cost method for assessing other individuals. Asymmetries in territorial counter‐singing interactions in songbirds provide a rich source of information for eavesdroppers about differences between the singers. Yet, little is known about the relationship between interactive singing in a natural, low‐arousal context among territorial neighbours and individual traits of males. We used a microphone array to monitor natural counter‐singing interactions in great tits (Parus major) during nest building, at the onset of the breeding season. We quantified song overlapping and song matching for 30 pairs (dyads) of interacting males, singing at their nest, respectively. We then compared these behaviours to five traits for 28 males: body condition, plumage ornamentation, offspring provisioning behaviour, offspring weight and breeding site quality. We found no relationship between a male song overlapping or matching behaviour and any of the measured traits. Therefore, our results do not support the idea that short‐term asymmetries in low‐arousal long‐range singing interactions among neighbours reflect differences in these fitness‐related traits. Instead, our findings suggest that such singing asymmetries have less signal value in the absence of an immediate conflict but instead reflect short‐term motivational differences, as shown in previous investigations.

Male aggressiveness during the female fertile phase in relation to extra-pair paternity, plumage ornaments and female traits

In many bird species, physical aggression between males become more frequent during the female’s fertile period, as female encounters with extra-pair males are more frequent and can entail paternity losses. Male aggressiveness during this stage has been proposed as crucial for ensuring male reproductive success. Thus, plumage ornaments could represent honest signals of individual quality that could reflect the aggressiveness of paired territorial males. Furthermore, male aggressiveness could be related to mate quality or defensive capacity. We quantified extra-pair paternity in the broods and investigated the association of male and female traits with the aggressive behaviour of territorial paired males in a Spanish population of Pied Flycatchers (Ficedula hypoleuca), where territorial intrusions were simulated during the female fertile period by placing a taxidermic male mount close to the nest. We predicted that (1) more aggressive males should better protect their mates from intruding males and thereby reduce their paternity losses, (2) males with larger white patches and higher UV reflectance of wing patches should respond more strongly to intrusions, and (3) that males should be more aggressive when mated with higher quality females. We found evidence that males that responded less intensely to a territorial intrusion suffered a higher paternity loss, which offers strong support to the basic tenet of the theory of territoriality as paternity defence. Moreover, both the level of male aggressiveness and control of the territory increased with male UV reflectance of wing patches. Finally, we found, contrary to our prediction, that males were less aggressive when mated with more ornamented females.

Male plumage signal expression is related to feather corticosterone concentration in the Pied Flycatcher Ficedula hypoleuca

Male signals may express the capacity to sustain environmental challenges. In some migratory birds like the Pied Flycatcher Ficedula hypoleuca, plumage ornaments are molted in the winter quarters shortly before spring migration while most feathers are replaced shortly after the breeding season in the breeding areas. The concentration of corticosterone in feathers (CORTf) may relate to baseline CORT levels at the time of molt which could be expressed through plumage signals. Male Pied Flycatchers present white patches on forehead feathers and tertials which are molted before spring migration and on secondaries and primaries replaced after breeding. They also express a variable degree of melanisation of head and back feathers molted in the wintering areas. All these plumage traits have been previously shown to function in social contests and/or mate attraction. Here we have collected tertials on the two wings and two tail feathers, molted in wintering and breeding areas respectively, of males in a Spanish montane population and analysed CORTf in the laboratory with standard enzyme immunoassays. There is no correlation within individuals between CORTf in the two types of feathers, although levels are similar. The size of the forehead patch is negatively associated with CORTf in tail feathers, mainly in small males, while the blackness of head and back is negatively related to CORTf in tertials, mainly in large males. The size of the wing patch composed of patches on feathers molted both in wintering (tertials) and breeding areas (primaries and secondaries) is not related to CORTf in any type of feather. Different male plumage traits thus may reflect circulating CORT levels during molt processes occurring in the wintering respectively breeding range as expressed by CORTf in different types of feathers.

Intersexual social dominance mimicry drives female hummingbird polymorphism.

Female-limited polymorphisms, where females have multiple forms but males have only one, have been described in a variety of animals, yet are difficult to explain because selection typically is expected to decrease rather than maintain diversity. In the white-necked jacobin (Florisuga mellivora), all males and approximately 20% of females express an ornamented plumage type (androchromic), while other females are non-ornamented (heterochromic). Androchrome females benefit from reduced social harassment, but it remains unclear why both morphs persist. Female morphs may represent balanced alternative behavioural strategies, but an alternative hypothesis is that androchrome females are mimicking males. Here, we test a critical prediction of these hypotheses by measuring morphological, physiological and behavioural traits that relate to resource-holding potential (RHP), or competitive ability. In all these traits, we find little difference between female types, but higher RHP in males. These results, together with previous findings in this species, indicate that androchrome females increase access to food resources through mimicry of more aggressive males. Importantly, the mimicry hypothesis provides a clear theoretical pathway for polymorphism maintenance through frequency-dependent selection. Social dominance mimicry, long suspected to operate between species, can therefore also operate within species, leading to polymorphism and perhaps similarities between sexes more generally.

Extra-pair paternity drives plumage colour elaboration in male passerines.

The elaborate ornamental plumage displayed by birds has largely been attributed to sexual selection, whereby the greater success of ornamented males in attaining mates drives a rapid elaboration of those ornaments. Indeed, plumage elaboration tends to be greatest in species with a high variance in reproductive success such as polygynous mating systems. Even among socially monogamous species, many males are extremely colourful. In their now-classic study, Møller and Birkhead (1994) suggested that increased variance in reproductive success afforded by extra-pair paternity should intensify sexual selection pressure and thus an elaboration of male plumage and sexual dichromatism, but the relatively few measures of extra-pair paternity at the time prevented a rigorous test of this hypothesis. In the nearly three decades since that paper's publication, hundreds of studies have been published on rates of extra-pair paternity and more objective measures of plumage colouration have been developed, allowing for a large-scale comparative test of Møller and Birkhead's (1994) hypothesis. Using an analysis of 186 socially monogamous passerine species with estimates of extra-pair paternity, our phylogenetically controlled analysis confirms Møller and Birkhead's (1994) early work, demonstrating that rates of extra-pair paternity are positively associated with male, but not female, colouration and with the extent of sexual dichromatism. Plumage evolution is complex and multifaceted, driven by phylogenetic, ecological, and social factors, but our analysis confirms a key role of extra-pair mate choice in driving the evolution of ornamental traits.

Phenotypic selection on an ornamental trait is not modulated by breeding density in a pied flycatcher population

Most studies of phenotypic selection in the wild have focussed on morphological and life‐history traits and looked at abiotic (climatic) variation as the main driver of selection. Consequently, our knowledge of the effects of biotic environmental variation on phenotypic selection on sexual traits is scarce. Population density can be considered a proxy for the intensity of intrasexual and intersexual competition and could therefore be a key factor influencing the covariation between individual fitness and the expression of sexual traits. Here, we used an individual‐based data set from a population of pied flycatchers (Ficedula hypoleuca) monitored over 24 years to analyze the effect of breeding density on phenotypic selection on dorsal plumage colouration, a heritable and sexually selected ornament in males of this species. Using the number of recruits as a fitness proxy, our results showed overall stabilizing selection on male dorsal colouration, with intermediate phenotypes being favoured over extremely dark and dull individuals. However, our results did not support the hypothesis that breeding density mediates phenotypic selection on this sexual trait. We discuss the possible role of other biotic factors influencing selection on ornamental plumage.

A tail of plumage colouration: disentangling geographic, seasonal and dietary effects on plumage colour in a migratory songbird

Plumage ornamentation in birds serves critical inter‐ and intra‐sexual signaling functions. While carotenoid‐based plumage colouration is often viewed as a classic condition‐dependent sexually selected trait, plumage colouration can be influenced by a wide array of both intrinsic and extrinsic factors. Understanding the mechanisms underlying variation in colouration is especially important for species where the signaling function of ornamental traits is complex or when the literature is conflicting. Here, we examined variation in the yellow/orange tail feathers of American redstarts Setophaga ruticilla passing through two migratory stopover sites in eastern North America during both spring and fall migration to assess the role of geographic variation and seasonality in influencing feather colouration. In addition, we investigated whether diet during moult (inferred via stable isotope analysis of feather δ15N and δ13C) influenced plumage colouration. Our findings indicate that geographic variation, season and diet all influence individual differences in American redstart colouration, represented by both traditional and tetrahedral colour variables. The extent to which these factors influence colour expression however is largely dependent on the colour metric under study, likely because different colour metrics reflect different attributes of the feather (e.g. structural components versus pigment deposition). The effects of diet (δ15N) and season were pronounced for brightness, suggesting a strong effect of diet and feather wear/degradation on feather structure. Though hue, a metric that should strongly reflect pigment deposition, also changed from spring to fall, that effect was dependent on age, with only adults experiencing a reduction in ornamentation. Taken together, our results highlight the numerous sources of variation behind plumage coloration and underscores the difficulty of unraveling complex visual signaling systems, such as those in American redstarts.

Evolutionary trade-off between male colouration and feather moult extent also indirectly determines female moult.

Males and females are often influenced by different selective forces, frequently resulting in diverging phenotypes, for example in colouration. Since an animal's colouration may strongly influence its fitness, causes and consequences of sexual dichromatism in birds could aid in understanding important factors affecting sexual and natural selection. Variation in plumage ornamentation may affect mate attraction or intraspecific antagonistic behaviour. In most passerines, body plumage colouration of juveniles is obtained through the process of feather moult. The number of moulted wing and tail feathers, which also influences the bird's appearance, may affect its fitness. Here, we show that body plumage colouration of male, but not female, passerines is correlated with the number of moulted wing and tail feathers in the early stage of the bird's life for both sexes. Thus, the extent of wing and tail moult in females is not modulated by the female's colouration and can prevent females from reaching their sex-specific optima. This result could be explained by high intersexual genetic correlations, which might make it impossible for the sexes to reach their own trait fitness optima. Our findings may indicate that species-specific, rather than sex-specific, internal correlations shaped bird moult strategy, an important avian life-history trait.

Correlated evolution of distinct signals associated with increased social selection in female white-shouldered fairywrens.

Conspicuous female signals have recently received substantial scientific attention, but it remains unclear if their evolution is the result of selection acting on females independently of males or if mutual selection facilitates female change. Species that express female, but not male, phenotypic variation among populations represents a useful opportunity to address this knowledge gap. White‐shouldered fairywrens (Malurus alboscapulatus) are tropical songbirds with a well‐resolved phylogeny where female, but not male, coloration varies allopatrically across subspecies. We explored how four distinct signaling modalities, each putatively associated with increased social selection, are expressed in two populations that vary in competitive pressure on females. Females in a derived subspecies (M. a. moretoni) have evolved more ornamented plumage and have shorter tails (a signal of social dominance) relative to an ancestral subspecies (M. a. lorentzi) with drab females. In response to simulated territorial intrusions broadcasting female song, both sexes of M. a. moretoni are more aggressive and more coordinated with their mates in both movement and vocalizations. Finally, M. a. moretoni songs are more complex than M. a. lorentzi, but song complexity does not vary between sexes in either population. These results suggest that correlated phenotypic shifts in coloration and tail morphology in females as well as song complexity and aggression in both sexes may have occurred in response to changes in the intensity of social selection pressures. This highlights increased competitive pressures in both sexes can facilitate the evolution of complex multimodal signals.

Inter-annual repeatability and age-dependent changes in plasma testosterone levels in a longitudinally monitored free-living passerine bird.

While seasonal trends in testosterone levels are known from cross-cohort studies, data on testosterone inter-annual individual repeatability in wild birds are rare. Also, our understanding of hormonal age-dependent changes in testosterone levels is limited. We assessed plasma testosterone levels in 105 samples originating from 49 repeatedly captured free-living great tits (Parus major) sampled during the nesting to investigate their relative long-term repeatability and within-individual changes. Furthermore, we examined the inter-annual repeatability of condition-related traits (carotenoid- and melanin-based plumage ornamentation, ptilochronological feather growth rate, body mass, and haematological heterophil/lymphocyte ratio) and their relationships to testosterone levels. We show that testosterone levels are inter-annually repeatable in females, with a non-significant pattern in males, both in absolute values and individual ranks (indicating the maintenance of relative status in a population). In males, we found a quadratic dependence of testosterone levels on age, with a peak in midlife. In contrast, female testosterone levels showed no age-dependent trends. The inter-annual repeatability of condition-related traits ranged from zero to moderate and was mostly unrelated to plasma testosterone concentrations. However, males with elevated testosterone had significantly higher carotenoid-pigmented yellow plumage brightness, a trait presumably involved in mating. Showing inter-annual repeatability in testosterone levels, this research opens the way to further understanding the causes of variation in condition-related traits. Based on a longitudinal dataset, this study demonstrates that male plasma testosterone undergoes age-related changes that may regulate resource allocation. Our results thus suggest that, unlike females, male birds undergo hormonal senescence similar to mammals.

Social and abiotic factors differentially affect plumage ornamentation of young and old males in an Australian songbird

Both abiotic environmental conditions and variation in social environment are known to impact the acquisition of sexual signals. However, the influences of abiotic environmental and social factors are rarely compared to each other. Here we test the relative importance of these factors in determining whether and when male red-backed fairy-wrens, Malurus melanocephalus , moult into ornamented breeding plumage , a known sexual signal. One-year-old male red-backed fairy-wrens vary in whether or not they acquire ornamentation, whereas males age 2 years and older vary in their timing of ornament acquisition. It is unclear whether these processes are determined by the same or different factors, and we examined both events using a combination of long-term breeding records and nonbreeding social networks. We found that 1-year-old males that paired prior to the start of the breeding season were more likely to acquire ornamented plumage, but rainfall did not influence whether 1-year-old males acquired ornamented plumage. Thus, for young individuals, social cues appear to play a larger role than abiotic environmental factors in determining ornament acquisition. For older males, timing of ornamented plumage acquisition was constrained by rainfall, with drier nonbreeding seasons leading to poorer physiological condition and later moult dates. Thus, sexual signal variation in older males appears to be a condition-dependent trait, driven by abiotic environmental and physiological factors rather than social cues. These findings reveal that factors influencing sexual signal expression can vary with age when age classes exhibit different forms of signal variation. Our results suggest that social environment may drive sexual signal variation in young individuals, whereas abiotic environmental variation may drive sexual signal variation in older individuals. • The factors influencing sexual signal expression remain unclear. • Social factors determined whether 1-year-old males acquired ornamented plumage. • Rainfall determined when older males acquired ornamented plumage. • Factors influencing sexual signal expression can vary with age.

Male-like ornamentation in female hummingbirds results from social harassment rather than sexual selection

Ornamentation is typically observed in sexually mature adults, is often dimorphic in expression, and is most apparent during breeding, supporting a role for sexual selection in its evolution.1-4 Yet, increasing evidence suggests that nonsexual social selection may also have a role in the evolution of ornamentation, especially in females.5-9 Distinguishing between these alternatives remains challenging because sexual and nonsexual factors may both play important and overlapping roles in trait evolution.7,10 Here, we show that female ornamentation in a dichromatic hummingbird, the white-necked jacobin (Florisuga mellivora), cannot be explained by sexual selection. Although all males are ornamented, nearly 30% of females have male-like plumage. Remarkably, all juveniles of both sexes express ornamented plumage similar to adult males (androchromatism), but 80% of females acquire non-ornamented plumage (heterochromatism) as they age. This unique ontogeny excludes competition for mates as an explanation for female ornamentation because non-reproductive juveniles are more likely to be ornamented than adults. Instead, avoidance of social harassment appears to underlie this female-limited polymorphism, as heterochrome taxidermy mounts received more aggressive and sexual attention than androchrome mounts from this and other hummingbird species. Monitoring electronically tagged birds at data-logging feeders showed that androchrome females accessed feeders more than heterochrome females, presumably because of reduced harassment. Our findings demonstrate that ornamentation can arise purely through nonsexual social selection, and this hypothesis must be considered in the evolution of not only female-limited polymorphism but also the spectacular ornamentation often assumed to result from sexual selection.

Ornamental Plumage Coloration Interacts with Habitat Urbanization to Predict Problem-Solving in the House Finch Haemorhous mexicanus

Urbanization presents wildlife with many novel environmental challenges and opportunities, including navigating new physical structures and exploiting unique food bases. Thus, animal species that persist or thrive in urban environments may have superior cognitive abilities that allow them to navigate and solve anthropogenic problems. Prior studies have shown neural and behavioral differences between animals inhabiting urban and rural environments, but few have tested cognition-related behavioral responses of animals in an urban context. We administered a novel foraging challenge to caged male House Finches Haemorhous mexicanus — a successful urban and native desert species in the southwestern United States — captured from two urban and two rural locations to examine population differences in problem solving. This task involved opening a tin lid that was slid over the bird's normal small food dish and left only slightly ajar (with no food visible). Male House Finches display exaggerated, sexually selected plumage color that is dependent on diet, so we also tested the hypothesis that more colorful males can better solve foraging problems. We found no differences in problem solving success between urban and rural birds. However, among rural birds, we found that redder males were more likely to solve the foraging task than less-red males. Also, birds that lost more mass during the study were more likely to solve the task, but this was only true among less colorful birds. Our results are consistent with the hypothesis that plumage redness reveals foraging skill in House Finches found in their native environment.

Wildfire affects expression of male sexual plumage through suppressed testosterone circulation in a tropical songbird

Natural disturbances like drought and wildfires are expected to increase in prevalence, so understanding how organisms are affected is a key goal for conservationists and biologists alike. While many studies have illustrated long‐term effects of perturbations on survival and reproduction, little is known of short‐term effects to physiology and sexual signal expression. Ornamental traits have been proposed as reliable indicators of environmental health, yet studies are lacking in the context of natural disturbances. Here we present short‐term (7–65 days) responses of male red‐backed fairywrens Malurus melanocephalus to wildfire near the onset of the typical breeding season. Young males of this species are characterized by plastic expression of sexual plumage phenotypes depending on circulating testosterone and body condition. Using two populations with fairywren captures before and after separate wildfires we illustrate that wildfire suppressed molt into ornamented plumage. Neither baseline plasma corticosterone or furcular fat stores were affected by fire. However, fire seemed to interfere with the termporal increase in plasma testosterone during the pre‐breeding season, leading to a lower proportion of males molting into ornamented plumage. Collectively, these findings suggest that wildfires inhibit or greatly delay acquisition of ornamentation in males through enduring suppression of testosterone circulation.

Female ornamentation, incubation behavior, and reproductive success in a wild bird

In many species, both males and females possess sexual signals, but most research focuses on understanding signal expression in males. Females are often assumed to possess signals as a non-functional by-product of selection on males, but increasing evidence demonstrates functional explanations for variation in female signals. Theory suggests that—for many bird species—differences in long-term fitness associated with female signaling are more likely to be driven by variation in offspring quality than quantity, but research paradigms developed for studying male signals have primarily focused on counting offspring produced. Here, we tested the hypothesis that female ornamentation reliably signals the ability to incubate effectively. We used temperature loggers placed in the nest of common yellowthroat warblers (Geothlypis trichas) to record incubation behavior across multiple breeding attempts. Incubation bout length and the onset of daily activity were highly variable between females, but repeatable within females across multiple nesting attempts. Females with longer bouts and later onset of activity had higher hatching success. Wing length and plumage coloration were not related to incubation length or onset of activity, but were correlated with the total percentage of time spent on the nest each day. However, there was only a trend for repeatability in percentage of time spent on the nest and this measure was not correlated with any metrics of offspring quality or hatching success that we recorded. Therefore, we did not find any single aspect of incubation behavior that was (i) consistent, (ii) related to nestling quality or success, and (iii) signaled by ornamentation. Our results demonstrate the importance of variation in incubation behavior, but also suggest that ornaments are of limited utility as a signal of incubation ability in this species. Nevertheless, our study highlights the need to explore alternative fitness proxies in order to understand variation in female ornamentation. Choosing a high-quality mate is an important determinant of reproductive success and animals often attend to elaborate ornaments as signals of quality during mate choice. In many species, both males and females have ornaments, but most research has focused on male signals and female mate choice. We found that female incubation behavior is associated with both plumage ornaments and hatching success, but there was no single signal that provided reliable information about the aspects of incubation behavior that were related to reproductive success. Our findings suggest that understanding female ornamentation may depend on considering the specific ways that females contribute to offspring survival.

Female and male plumage color is linked to parental quality, pairing, and extrapair mating in a tropical passerine

AbstractSexual selection has been proposed to drive the evolution of elaborate phenotypic traits in males, which often confer success in competition or mating. However, in many species, both males and females display such traits. Studies examining how selection acts on both sexes are scarce. In this study, we investigated whether plumage ornamentation is sexually selected in females and males lovely fairy-wren Malurus amabilis, a cooperatively breeding songbird. We found that female and male plumage color was correlated with parental quality but not with individual quality or survival. We also found evidence of positive assortative mating based on plumage color. Microsatellite analyses of paternity indicated that the lovely fairy-wren has high levels of extrapair paternity (EPP), with 53% of offspring (in 58% of broods of 57% of females) resulting from extrapair (EP) mating. Female and male plumage color did not predict reproductive success or the proportion of EP offspring in their own nest, but less colorful males obtained higher EPP when paired with more colorful females and gained overall higher total paternity (own nest and other nests). We argue that plumage color may be under sex-specific selection, highlighting the importance of looking at both sexes in studies of sexual selection and ornament evolution. The current findings together with the previous study suggest that plumage color in female and male lovely fairy-wrens appears to be an honest signal relevant in both intrasexual and intersexual competition contexts.

Genomic Insights Into the Molecular Basis of Sexual Selection in Birds

Sexual selection is a well-known biological process, yet the genomic basis and patterns of sexual selection are not fully understood. The extravagant ornamental plumage of peacock (Pavo cristatus) was instrumental in shaping Charles Darwin's theory of sexual selection and is considered to be an honest signal of its immunocompetence. Here, we used the recently generated draft genome sequence of peafowl (Pavo cristatus) and carried out a comparative analysis across 11 bird genomes that encompass a range of sexual selection and also had high-quality genomic and phenotypic data publically available to study the genomic basis of sexual selection. We found that varying degree of purifying selection was the predominant mechanism of action for sexual selection at the genome-wide scale and observed that sexual selection mostly influences genes regulating gene expression and protein processing. Specifically, the genome-wide phylogenetically corrected regression analysis supported the continuous or ongoing model of sexual selection. Genes involved in nucleic acid binding and gene expression regulation, including a specific regulator of sex-determination known as TRA2A to be under positive selection in the species with high post-copulatory sexual selection manifested as high sperm competition. We also detected specific feather-related and immune-related gene-pairs evolving under similar selection pressures across the 11 species, including peacock (Pavo cristatus), which is consistent with the Hamilton-Zuk hypothesis. The comparative genomics analysis of 11 avian taxa has provided new insights on the molecular underpinnings of sexual selection and identifies specific genomic regions for future in-depth analysis.