Testosterone accelerates the onset of photorefractoriness in baya weaver Ploceus philippinus.

The baya weaver Ploceus philippinus, despite its purely tropical origin and tropical/subtropical distribution, exhibits all features of a typically photoperiodic species. The onset of reproduction in this species is triggered by increasing daylength and breeding is terminated by the development of distinct photorefractory phase. In order to ascertain the involvement of androgens in the development of photorefractoriness the long day response of birds was tested after a prior exposure to varied doses of testosterone. Testosterone treatment accelerated the onset of photorefractoriness as judged from the gonadal status, LH-dependent yellow plumage and testosterone-dependent beak pigmentation. While gonadal development and yellow plumage occurred in the control birds due to the stimulatory long photoperiod, the testosterone administered birds failed to show such developments. These findings indicate that testosterone might impair the higher photoresponding mechanisms resulting in the development of photorefractoriness.     

The influence of parasites on host sexual selection

In 1982 Hamilton and Zuk(1) proposed a provocative solution for the unexplained fact that the males of many species exhibit 'showy' traits such as brightly coloured plumage or vigorous courtship displays. They suggested that showy traits are fully expressed only by males who are resistant to parasites and that females examine such traits in order to choose resistant males as mates. Hamilton and Zuk's proposal has been the topic of extensive research and vigorous debate for nearly a decade. This article reviews the research, relevant criticisms and unanswered questions pertaining to the influence of parasites on sexual selection.     

Effects of testosterone on growth, plumage pigmentation, and mortality in Black-headed Gull chicks

In the Black-headed Gull Larus ridibundus, sibling chicks defend small territories against conspecifics with testosterone-dependent aggressive behaviour. The energetic requirements for the performance of this behaviour may trade off against the energetic requirements for growth. There are indications that testosterone suppresses growth in birds and, therefore, regulate this trade-off. In this study, the effect of testosterone on growth and plumage pigmentation of Black-headed Gull chicks was analysed. Young chicks in small groups were treated for ten days with testosterone or sham treated. Testosterone-treated birds showed decreased growth rate (daily increase in body mass, head-bill length and tarsus-length) and a marked decrease in juvenile pigmentation of the plumage (tail-bar, back, and secondary coverts). Field measurements revealed a negative correlation between nest density, which correlates positively with aggressive behaviour of adults, and plumage coloration. Furthermore, these measurements showed an increase in mortality of chicks that had low levels of pigmentation early in life. The data suggest that chicks face a testosterone-regulated trade-off between growth and territory defence.     

Hormonal differentiation of sexual behavior in Japanese quail

The effect of hormones on the development of Japanese quail during the postembryonic period was examined. First, subcutaneous implants of estradiol monobenzoate (EB) and testosterone propionate (TP) were implanted 6–12 hr after hatching. EB and TP had no effect on the differentiation of sexual behavior in genetic males or females. However, EB had marked feminizing effects on plumage in genetic males. Second, the role of gonadal hormones during development was examined by gonadectomizing males and females 6–12 hr after hatching and treating them intramuscularly with EB or TP as adults. EB-treated adult females displayed sexual behavior typical of the genetic female and developed female plumage. A significant proportion of TP-treated females (57%) displayed male sexual behavior patterns. Cloacal gland development and male-type vocalizations were induced. EB-treated males displayed either male or female sexual patterns depending on the stimulus conditions. Third, to test whether bisexuality in gonadectomized males and females is maintained despite steroid treatment and expression of sexual behavior in adulthood, gonadectomized quail which were originally treated with EB received TP and vice versa. The results indicate that in the absence of gonadal hormones after hatching female quail remain bisexual until exposed to estrogen, whereas gonadectomized male quail retain behavioral bisexuality irrespective of prior estrogen or androgen exposure.     

Coming of age in fringillid birds: heterochrony in the ontogeny of secondary sexual characters

The great variation in the timing of development of adult plumages in North American male passerine birds has in recent years provoked much theoretical interest. It has commonly been assumed that the heterochronic process involved is invariably a retardation of the development of adult plumages. On the basis of a phylogenetic analysis of the nine-primaried oscines (Fringillidae), I suggest that the heterochronic process that has operated most frequently in North American taxa is not a retardation, but an acceleration. I also suggest that sexual dimorphism in plumage, and late plumage maturation in males, may arise as a secondary result of selection for neoteny in females with a correlated response in males, and not necessarily, as traditionally thought, as a result of selection for bright plumages in males.     

Reversed plumage ontogeny in a female hummingbird: implications for the evolution of iridescent colours and sexual dichromatism

In polygynous birds, bright plumage is typically more extensive in the sexually competitive males and develops at or after sexual maturity. These patterns, coupled with the importance of male plumage in sexual displays, fostered the traditional hypothesis that bright plumages and sexual dichromatism develop through the actions of sexual selection on males. This view remains problematic for hummingbirds, all of which are polygynous, because their bright iridescent plumages are also important non-sexual signals associated with dominance at floral nectar sources. Here I show that female amethyst-throated sunangels [ Heliangelus amethysticollis (d'Orbigny & Lafresnaye)], moult from an immature plumage with an iridescent gorget to an adult plumage with a non-iridescent gorget. This 'reversed' ontogeny contradicts the notion that iridescent plumage has a sexual function because sexual selection in polygynous birds should be lowest among non-reproductive immature females. Moreover, loss of iridescent plumage in adult females indicates that adult sexual dichromatism in H. amethysticollis is due in large part to changes in female ontogeny. I suggest that both the ontogeny and sexual dichromatism evolved in response to competition for nectar.     

Evolutionary drivers of seasonal plumage colours: colour change by moult correlates with sexual selection,predation risk and seasonality across passerines

Some birds undergo seasonal colour change by moulting twice each year, typically alternating between a cryptic, non‐breeding plumage and a conspicuous, breeding plumage (‘seasonal plumage colours’). We test for potential drivers of the evolution of seasonal plumage colours in all passerines (N = 5901 species, c. 60% of all birds). Seasonal plumage colours are uncommon, having appeared on multiple occasions but more frequently lost during evolution. The trait is more common in small, ground‐foraging species with polygynous mating systems, no paternal care and strong sexual dichromatism, suggesting it evolved under strong sexual selection and high predation risk. Seasonal plumage colours are also more common in species predicted to have seasonal breeding schedules, such as migratory birds and those living in seasonal climates. We propose that seasonal plumage colours have evolved to resolve a trade‐off between the effects of natural and sexual selection on colouration, especially in seasonal environments.     

Testosterone treatment of female Superb Fairy-wrens Malurus cyaneus induces a male-like prenuptial moult, but no coloured plumage

When selection strongly favours a testosterone-dependent trait in males, and this trait is not beneficial to females, a correlated response to selection in females, which also circulate some testosterone, could slow the rate of evolution in males. Here I investigate whether experimental testosterone treatment in female Superb Fairy-wrens Malurus cyaneus can induce the testosterone-dependent sexually selected moult into nuptial plumage, as it does in males. Silastic testosterone implants in females rapidly induced a moult akin to the male prenuptial moult, involving all body areas that are colourful in nuptial males (head, upper back, ear tufts, breast). Moreover, the newly moulted feathers had a similar glistening appearance and morphology as male nuptial feathers. However, the treatment failed to induce production of the blue and black structural colours, and the breast and ear tufts were lighter than the normal grey-brown feathers of females and males in eclipse plumage. Microscopic and ultrastructural analyses of these unusual feathers could further our understanding of structural colour production.     

The role of sexual and natural selection in shaping patterns of sexual dichromatism in the largest family of songbirds (Aves: Thraupidae)

Males and females can be under different evolutionary pressures if sexual and natural selection is differentially operating in each sex. As a result, many species have evolved sexual dichromatism, or differences in coloration between sexes. Although sexual dichromatism is often used as an index of the magnitude of sexual selection, sexual dichromatism is a composite trait. Here, we examine the evolution of sexual dichromatism in one of the largest and most ecologically diverse families of birds, the tanagers, using the avian visual perspective and a species‐level phylogeny. Our results demonstrate that the evolutionary decreases of sexual dichromatism are more often associated with larger and more frequent changes in male plumage coloration, and evolutionary increases are not more often associated with larger changes in either sex. Furthermore, we show that the crown and ventral plumage regions are correlated with sexual dichromatism in males, and that only male plumage complexity is positively correlated with sexual dichromatism. Finally, we demonstrate that light environment is important in shaping both plumage brilliance and complexity. By conducting a multilevel analysis of plumage evolution in males and females, we show that sexual dichromatism evolves via a mosaic of sexual and natural selection in both sexes.     

Mating systems, sperm competition, and the evolution of sexual dimorphism in birds

Comparative analyses suggest that a variety of factors influence the evolution of sexual dimorphism in birds. We analyzed the relative importance of social mating system and sperm competition to sexual differences in plumage and body size (mass and tail and wing length) of more than 1,000 species of birds from throughout the world. In these analyses we controlled for phylogeny and a variety of ecological and life-history variables. We used testis size (corrected for total body mass) as an index of sperm competition in each species, because testis size is correlated with levels of extrapair paternity and is available for a large number of species. In contrast to recent studies, we found strong and consistent effects of social mating system on most forms of dimorphism. Social mating system strongly influenced dimorphism in plumage, body mass, and wing length and had some effect on dimorphism in tail length. Sexual dimorphism was relatively greater in species with polygynous or lekking than monogamous mating systems. This was true when we used both species and phylogenetically independent contrasts for analysis. Relative testis size was also related positively to dimorphism in tail and wing length, but in most analyses it was a poorer predictor of plumage dimorphism than social mating system. There was no association between relative testis size and mass dimorphism. Geographic region and life history were also associated with the four types of dimorphism, although their influence varied between the different types of dimorphism. Although there is much interest in the effects of sperm competition on sexual dimorphism, we suggest that traditional explanations based on social mating systems are better predictors of dimorphism in birds.     

Plumage colour in nestling blue tits: sexual dichromatism,condition dependence and genetic effects

Sexual-selection theory assumes that there are costs associated with ornamental plumage coloration. While pigment-based ornaments have repeatedly been shown to be condition dependent, this has been more difficult to demonstrate for structural colours. We present evidence for condition dependence of both types of plumage colour in nestling blue tits (Parus caeruleus). Using reflectance spectrometry, we show that blue tit nestlings are sexually dichromatic, with males having more chromatic (more 'saturated') and ultraviolet (UV)-shifted tail coloration and more chromatic yellow breast coloration. The sexual dimorphism in nestling tail coloration is qualitatively similar to that of chick-feeding adults from the same population. By contrast, the breast plumage of adult birds is not sexually dichromatic in terms of chroma. In nestlings, the chroma of both tail and breast feathers is positively associated with condition (body mass on day 14). The UV/blue hue of the tail feathers is influenced by paternally inherited genes, as indicated by a maternal half-sibling comparison. We conclude that the expression of both carotenoid-based and structural coloration seems to be condition dependent in blue tit nestlings, and that there are additional genetic effects on the hue of the UV/blue tail feathers. The signalling or other functions of sexual dichromatism in nestlings remain obscure. Our study shows that nestling blue tits are suitable model organisms for the study of ontogenetic costs and heritability of both carotenoid-based and structural colour in birds.     

Development and maturation of plumage in the wandering albatross Diomedea exulans

Changes in the plumage of the wandering albatross Diomedea exulans were studied on the Crozet Islands, using a population of birds of known sex and age and including some birds more than 32 years old. Plumage phases of a cross-section of the male and female populations are presented. Males and females fledge with a dark brown plumage. Between the first and fourth year the male's plumage becomes much whiter than the female's. Between five and 15–18 years old the whitening of plumage in either sex develops in parallel though still separated by the extent of the initial divergence. Male plumage probably attains a definitive snowy stage after 30 years while the plumage of the female does not mature beyond an intermediate stage, which is reached after 20 to 25 years. Maturation of the plumage of head, back and wing are compared. In birds of similar age, breeding birds tend to have a whiter plumage than non-breeders. In the oceanic range of the species, white birds, i.e. mostly adult males, favour cold antarctic waters while dark birds, i.e. mostly adult females and juveniles, are observed in warmer subtropical and subantarctic waters. We discuss the possible adaptive significance of the slow maturation in the plumage of the wandering albatross and of the differences in plumage between sexes and between populations.     

Unusual feather structure allows partial plumage wettability in diving great cormorants Phalacrocorax carbo

The great cormorant Phalacrocorax carbo is thought to have a wettable plumage, providing low body insulation during foraging. Great cormorants should thus be constrained by water temperatures, and show high energy requirements. Surprisingly, this species has one of the widest breeding distributions of all diving birds, and does not require more food than these other species. We explored this apparent paradox by comparing the insulative properties of body plumage in four subspecies of great cormorants ranging from tropical to polar regions. We found that all subspecies retained an insulating air layer in their plumage, which was, however, much thinner than for other species of diving birds. Detailed examination of the plumage showed that each cormorant body feather has a loose, instantaneously wet, outer section and a highly waterproof central portion. This indicates that the plumage of great cormorants is only partly wettable, and that birds maintain a thin layer of air in their plumage. Our findings suggest an unusual morphological-functional adaptation to diving which balances the antagonist constraints of thermoregulation and buoyancy.     

Wettability of juvenile plumage as a major cause of mortality threatens endangered Barau's petrel

Seabirds spend most of their life at sea and have to possess a waterproof plumage to be able to sit on water for extended periods. We tracked juvenile Barau's petrels for the first time, when they leave their birth colony and found that half of the transmitters stopped soon after they first landed on the water off Réunion Island. We suspected from observation at sea that birds may have problems with the waterproofness of their plumage. Therefore during the next season we set up a simple protocol to assess waterproofness of the plumage of the birds just before they fledge. This protocol is based on the calculation of a wettability index expressed as the mass of water logged in the plumage after simulating the bird sitting on the sea surface. We found that at least one third of chicks ready to fledge gained more than 4 g of water in 20 s, indicating that plumage was not waterproof. Within a sample of birds having fledged and before reaching the sea surface, a similar proportion of birds had their plumage not waterproof. For the birds tracked, only those with an index indicating a waterproof plumage successfully dispersed after their first touch on the sea surface. We provide evidence of a possible major cause of mortality of juvenile seabirds that has not been described previously in wild seabirds, but could exist in other species. This issue may be a major cause of threat to the endangered Barau's petrel.     

Pathways to elaboration of sexual dimorphism in bird plumage patterns

Patterns, such as bars and spots, are common in birds. Some patterns can function in camouflage and/or communication and can benefit both males and females, paving the way for elaboration in sexual dimorphism. Historically, sexual dichromatism was predominantly considered to be a consequence of mating systems. However, the distribution of traits between the sexes is not always indicative of function; genetic correlation may cause traits to evolve in both sexes and traits may serve a social function in males and/or females. In addition, sexual dichromatism in bird plumage patterns can be composed of multiple types of patterns within and/or between the sexes. Therefore, there can be more than one type of dimorphism and some are more elaborate than others. Under classical models of genetic correlation, patterns evolve in both sexes followed by a loss of patterning in one sex. Elaborate types of sexual dimorphism in plumage patterns may be due to selection acting on existing patterns and are perhaps derived. Waterfowl (Anseriformes) and gamebirds (Galliformes) arguably have the most striking plumage patterns. Using 288 species from these orders I reconstructed the evolutionary history of plumage pattern dimorphism. There was little support for genetic correlation but elaborate types of dimorphism are probably derived. Backward and forward evolutionary transitions between different types of dimorphism can occur by loss or elaboration. These results demonstrate that plumage patterns are evolutionary labile and current forms may represent shifting adaptations to a changing environment. © 2013 The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 111 , 262–273.     

Melanin‐based sexual dichromatism in the Western Palearctic avifauna implies darker males and lighter females

Melanins are the most common pigments providing coloration in the plumage and bare skin of birds and other vertebrates. Numerous species are dichromatic in the adult or definitive plumage, but the direction of this type of sexual dichromatism (i.e. whether one sex tends to be darker than the other) has not been thoroughly investigated. Using color plates, we analysed the presence of melanin‐based color patches in 666 species belonging to 69 families regularly breeding in the Western Palearctic. Sexual dichromatism based on melanins in at least one integumentary part involved 205 (30.7%) species. The body parts contributing more frequently to dichromatism were the dorsal areas, head and breast, whereas the less dichromatic body parts were the belly and the exposed integumentary parts (i.e. bill and legs). Regarding the phylogenetic spread of dichromatisms, 37 (53.6%) families contained at least one species with melanin‐based sexual dimorphism in the definitive adult plumage. As for the direction of the color difference, males are darker than females in a majority of species, meaning that males tend to produce more eumelanin and females tend to synthesize more pheomelanin. This survey has revealed the high prevalence of melanins in the emergence of sexual dichromatism in birds, at least in the Western Palearctic. Whether the described pattern is due to sexual selection promoting more conspicuous males or to natural selection for more cryptic females remains to be determined. Given that pheomelanin synthesis concurrently consumes the antioxidant glutathione but may also reduces toxic cysteine, sex‐biased physiological factors should also be given consideration in the evolution of bird plumages.     

The effects of elevated testosterone on plumage hue in male House Finches

The majority of studies examining the role of hormones in the proximate mechanisms of plumage coloration in birds have focused on intersexual differences (plumage dichromatism) and on structural- or melanin-based plumage coloration. The relationship between hormones and carotenoid-based plumage color, and in particular intrasexual plumage color variation, has received little attention. We manipulated testosterone levels of both captive and wild male House Finches to determine whether testosterone influences the expression of male plumage color in this species. We found that in captive male House Finches elevated testosterone delayed molt and resulted in drabber, less red plumage, even when birds were supplemented with dietary carotenoids. Elevated testosterone also resulted in drab plumage color in wild males, and appeared to delay molt in wild birds as well. Wild males implanted with testosterone showed wide variation in expression of plumage coloration. Those implanted early in the year molted plumage similar in color to their pre-treatment plumage, but those implanted later molted substantially duller plumage, possibly because delayed molt resulting from elevated testosterone caused these males to molt when carotenoid pigments were not available in sufficient amounts. These observations have the potential to explain previously reported relationships between plumage color and behavior in male House Finches, and highlight the importance of considering the proximate mechanisms of plumage coloration in avian sexual selection.     

Evolution of sexual dichromatism: contribution of carotenoid- versus melanin-based coloration

In birds, carotenoid-based plumage coloration is more dependent on physical condition and foraging abilities and less constrained developmentally than is melanin-based coloration. Thus, female mate choice for honest signals should result in more intense sexual selection on carotenoid- than on melanin-based plumage coloration. Using variation in sexual dimorphism as an indirect measure of the intensity of sexual selection, we tested the prediction mat variation in sexual dimorphism is driven more by change in carotenoid-based coloration between males and females dian by change in melanin-based coloration. Examination of historical changes in carotenoid- versus melanin-based pigmentation in 126 extant species of Cardueline finches supported this prediction. We found that carotenoid-derived coloration changed more frequendy among congeners dian melanin-based coloration. In both sexes, increase in carotenoid-based coloration score, but not in melanin-based coloration score, was strongly associated with increase in sexual dichromatism. In addition, sexual dimorphism in carotenoid-based coloration contributed more to overall dichromatism than dimorphism in melanin-based plumage. Our results supported die hypothesis that melanin-based and carotenoid-based coloration have fundamentally different signal content and suggest that combining melanin-based and carotenoid-based coloration in comparative analyses is not appropriate.     

Secondary poisoning of stoats (Mustela erminea), feral ferrets (Mustela furo), and feral house cats (Felis catus) by the anticoagulant poison,brodifacoum

Abstract

The extent of darkening of melanin‐based plumages in birds has previously been linked with increasing aggressive encounters between individuals. The North Island robin (Petroica longipes) is a territorial New Zealand endemic passerine that displays delayed plumage maturation (darkening of the plumage with age). Aggressive boundary interactions in the robin are relatively common during the breeding season, when territories are protected and juveniles are dispersing. This study tests the hypothesis of aggression‐mediated plumage darkening in a population of North Island robins by examining if males and older (darker) birds are either (1) involved in a higher number of aggressive interactions, or (2) are more often the aggressor than females and younger birds. When sex and age are accounted for, darker individuals will be either (3) involved in a higher number of interactions or (4) more often the aggressor in encounters with other individuals. Data were collected by scoring the plumage darkness of 32 individuals in the field, and observing (1) interaction behaviours, and (2) age and sex of the birds involved in each interaction. The results show no support for any aggression‐mediated plumage darkness in the robin; males and older birds were not involved in more aggressive interactions, and were not more often the aggressor; and neither the frequency of interactions or the number of aggressive interactions were correlated with a darker plumage. Other more complex mechanisms may explain delayed plumage darkness in the North Island robin.     

Coccidial infection does not influence preening behavior in American goldfinches

Preening behavior in birds is important for the maintenance of thermoregulatory and ornamental functions of plumage. It has been repeatedly demonstrated that birds trade off time between plumage maintenance and other activities. However, the condition-dependent constraints of preening remain virtually unstudied. Here, we present the first experimental test of the hypothesis that intestinal parasite infection impairs preening activity. We studied male American goldfinches (Spinus tristis), a species with carotenoid-based plumage coloration. Following pre-alternate (spring) molt, we manipulated the health of males by infecting some birds with Isospora spp. coccidia and keeping others free of the infection. Although the goldfinches increased preening throughout the captive period, we found no significant effect of coccidial treatment on preening behavior. The effect of coccidia on plumage maintenance may be more pronounced under natural conditions where birds have limited access to food and engage in more activities that might limit time available for preening.